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<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX1987245" alias="T_CAR1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987245</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CAR1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Carteriospongia foliascens (Porifera): Field Control</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591257">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591257</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436735</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CAR1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987246" alias="T_CAR2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987246</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CAR2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Carteriospongia foliascens (Porifera): Field Control</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591258">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591258</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436736</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CAR2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987247" alias="T_CAR13">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987247</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CAR13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Carteriospongia foliascens (Porifera): 0mg/L; Recovery</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591259">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591259</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436745</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CAR13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987248" alias="T_COS43">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987248</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_COS43</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Coscinoderma matthewsi (Porifera): 30mg/L; Recovery</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591260">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591260</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436835</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_COS43</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987249" alias="T_COS44">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987249</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_COS44</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Coscinoderma matthewsi (Porifera): 30mg/L; Recovery</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591261">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591261</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436836</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_COS44</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987250" alias="T_COS45">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987250</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_COS45</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Coscinoderma matthewsi (Porifera): 30mg/L; Recovery</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591262">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591262</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436837</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_COS45</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987251" alias="T_COS46">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987251</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_COS46</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Coscinoderma matthewsi (Porifera): 30mg/L; Recovery</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591263">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591263</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436838</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_COS46</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987252" alias="T_COS47">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987252</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_COS47</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Coscinoderma matthewsi (Porifera): 30mg/L; Recovery</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591264">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591264</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436839</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_COS47</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987253" alias="T_COS48">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987253</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_COS48</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Coscinoderma matthewsi (Porifera): 30mg/L; Week4</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591265">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591265</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436840</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_COS48</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987254" alias="T_COS49">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987254</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_COS49</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Coscinoderma matthewsi (Porifera): 30mg/L; Week4</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591266">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591266</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436841</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_COS49</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987255" alias="T_COS50">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987255</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_COS50</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Coscinoderma matthewsi (Porifera): 30mg/L; Week4</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591267">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591267</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436842</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_COS50</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987256" alias="T_COS51">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987256</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_COS51</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Coscinoderma matthewsi (Porifera): 30mg/L; Week4</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591268">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591268</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436843</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_COS51</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987257" alias="T_COS52">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987257</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_COS52</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Coscinoderma matthewsi (Porifera): 30mg/L; Week4</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591269">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591269</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436844</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_COS52</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987258" alias="T_CAR14">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987258</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CAR14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Carteriospongia foliascens (Porifera): 0mg/L; Recovery</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591270">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591270</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436746</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CAR14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987259" alias="T_COS53">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987259</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_COS53</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Coscinoderma matthewsi (Porifera): 100mg/L; Recovery</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591271">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591271</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436845</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_COS53</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987260" alias="T_COS54">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987260</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_COS54</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Coscinoderma matthewsi (Porifera): 100mg/L; Recovery</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591272">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591272</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436846</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_COS54</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987261" alias="T_COS55">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987261</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_COS55</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Coscinoderma matthewsi (Porifera): 100mg/L; Recovery</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591273">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591273</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436847</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_COS55</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987262" alias="T_COS56">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987262</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_COS56</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Coscinoderma matthewsi (Porifera): 100mg/L; Recovery</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591274">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591274</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436848</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_COS56</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987263" alias="T_COS57">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987263</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_COS57</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Coscinoderma matthewsi (Porifera): 100mg/L; Recovery</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591275">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591275</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436849</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_COS57</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987264" alias="T_COS58">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987264</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_COS58</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Coscinoderma matthewsi (Porifera): 100mg/L; Week4</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591276">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591276</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436850</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_COS58</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987265" alias="T_COS59">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987265</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_COS59</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Coscinoderma matthewsi (Porifera): 100mg/L; Week4</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591277">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591277</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436851</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_COS59</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987266" alias="T_COS60">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987266</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_COS60</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Coscinoderma matthewsi (Porifera): 100mg/L; Week4</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591278">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591278</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436852</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_COS60</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987267" alias="T_COS61">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987267</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_COS61</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Coscinoderma matthewsi (Porifera): 100mg/L; Week4</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591279">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591279</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436853</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_COS61</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987268" alias="T_COS62">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987268</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_COS62</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Coscinoderma matthewsi (Porifera): 100mg/L; Week4</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591280">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591280</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436854</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_COS62</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987270" alias="T_CAR15">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987270</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CAR15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Carteriospongia foliascens (Porifera): 0mg/L; Recovery</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591281">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591281</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436747</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CAR15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987272" alias="T_CYM1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987272</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CYM1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Cymbastela coralliophila (Porifera): Field Control</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591282">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591282</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436855</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CYM1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987273" alias="T_CYM2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987273</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CYM2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Cymbastela coralliophila (Porifera): Field Control</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591283">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591283</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436856</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CYM2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987274" alias="T_CYM3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987274</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CYM3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Cymbastela coralliophila (Porifera): Field Control</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591284">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591284</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436857</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CYM3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987275" alias="T_CYM4">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987275</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CYM4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Cymbastela coralliophila (Porifera): Field Control</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591285">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591285</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436858</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CYM4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987276" alias="T_CYM5">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987276</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CYM5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Cymbastela coralliophila (Porifera): Field Control</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591286">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591286</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436859</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CYM5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987277" alias="T_CYM7">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987277</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CYM7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Cymbastela coralliophila (Porifera): Time0 Control</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591287">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591287</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436860</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CYM7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987278" alias="T_CYM8">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987278</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CYM8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Cymbastela coralliophila (Porifera): Time0 Control</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591288">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591288</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436861</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CYM8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987279" alias="T_CYM9">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987279</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CYM9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Cymbastela coralliophila (Porifera): Time0 Control</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591289">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591289</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436862</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CYM9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987280" alias="T_CYM10">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987280</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CYM10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Cymbastela coralliophila (Porifera): Time0 Control</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591290">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591290</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436863</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CYM10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987281" alias="T_CYM11">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987281</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CYM11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Cymbastela coralliophila (Porifera): Time0 Control</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591291">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591291</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436864</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CYM11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987282" alias="T_CAR16">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987282</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CAR16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Carteriospongia foliascens (Porifera): 0mg/L; Recovery</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591293">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591293</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436748</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CAR16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987283" alias="T_CYM13">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987283</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CYM13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Cymbastela coralliophila (Porifera): 0mg/L; Recovery</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591292">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591292</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436865</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CYM13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987284" alias="T_CYM14">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987284</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CYM14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Cymbastela coralliophila (Porifera): 0mg/L; Recovery</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591294">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591294</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436866</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CYM14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987285" alias="T_CYM15">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987285</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CYM15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Cymbastela coralliophila (Porifera): 0mg/L; Recovery</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591297">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591297</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436867</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CYM15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987286" alias="T_CYM16">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987286</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CYM16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Cymbastela coralliophila (Porifera): 0mg/L; Recovery</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591296">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591296</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436868</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CYM16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987287" alias="T_CYM17">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987287</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CYM17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Cymbastela coralliophila (Porifera): 0mg/L; Recovery</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591295">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591295</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436869</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CYM17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987288" alias="T_CYM18">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987288</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CYM18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Cymbastela coralliophila (Porifera): 0mg/L; Week4</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591298">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591298</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436870</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CYM18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987289" alias="T_CYM19">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987289</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CYM19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Cymbastela coralliophila (Porifera): 0mg/L; Week4</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591299">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591299</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436871</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CYM19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987290" alias="T_CYM20">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987290</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CYM20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Cymbastela coralliophila (Porifera): 0mg/L; Week4</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591300">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591300</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436872</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CYM20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987291" alias="T_CYM21">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987291</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CYM21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Cymbastela coralliophila (Porifera): 0mg/L; Week4</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591301">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591301</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436873</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CYM21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987292" alias="T_CYM22">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987292</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CYM22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Cymbastela coralliophila (Porifera): 0mg/L; Week4</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591302">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591302</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436874</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CYM22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987293" alias="T_CAR17">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987293</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CAR17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Carteriospongia foliascens (Porifera): 0mg/L; Recovery</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591303">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591303</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436749</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CAR17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987294" alias="T_CYM43">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987294</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CYM43</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Cymbastela coralliophila (Porifera): 30mg/L; Recovery</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591304">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591304</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436875</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CYM43</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987295" alias="T_CYM44">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987295</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CYM44</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Cymbastela coralliophila (Porifera): 30mg/L; Recovery</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591305">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591305</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436876</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CYM44</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987296" alias="T_CYM45">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987296</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CYM45</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Cymbastela coralliophila (Porifera): 30mg/L; Recovery</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591306">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591306</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436877</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CYM45</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987297" alias="T_CYM46">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987297</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CYM46</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Cymbastela coralliophila (Porifera): 30mg/L; Recovery</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591307">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591307</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436878</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CYM46</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987298" alias="T_CYM47">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987298</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CYM47</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Cymbastela coralliophila (Porifera): 30mg/L; Recovery</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591308">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591308</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436879</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CYM47</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987299" alias="T_CYM48">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987299</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CYM48</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Cymbastela coralliophila (Porifera): 30mg/L; Week4</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591309">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591309</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436880</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CYM48</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987300" alias="T_CYM49">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987300</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CYM49</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Cymbastela coralliophila (Porifera): 30mg/L; Week4</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591310">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591310</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436881</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CYM49</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987301" alias="T_CYM50">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987301</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CYM50</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Cymbastela coralliophila (Porifera): 30mg/L; Week4</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591311">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591311</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436882</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CYM50</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987302" alias="T_CYM51">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987302</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CYM51</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Cymbastela coralliophila (Porifera): 30mg/L; Week4</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591312">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591312</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436883</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CYM51</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987303" alias="T_CYM52">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987303</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CYM52</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Cymbastela coralliophila (Porifera): 30mg/L; Week4</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591313">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591313</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436884</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CYM52</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987304" alias="T_CAR18">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987304</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CAR18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Carteriospongia foliascens (Porifera): 0mg/L; Week4</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591314">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591314</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436750</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CAR18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987305" alias="T_CYM53">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987305</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CYM53</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Cymbastela coralliophila (Porifera): 100mg/L; Recovery</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591315">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591315</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436885</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CYM53</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987306" alias="T_CYM54">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987306</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CYM54</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Cymbastela coralliophila (Porifera): 100mg/L; Recovery</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591316">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591316</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436886</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CYM54</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987307" alias="T_CYM55">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987307</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CYM55</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Cymbastela coralliophila (Porifera): 100mg/L; Recovery</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591317">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591317</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436887</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CYM55</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987308" alias="T_CYM56">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987308</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CYM56</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Cymbastela coralliophila (Porifera): 100mg/L; Recovery</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591318">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591318</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436888</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CYM56</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987309" alias="T_CYM57">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987309</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CYM57</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Cymbastela coralliophila (Porifera): 100mg/L; Recovery</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591319">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591319</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436889</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CYM57</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987310" alias="T_CYM58">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987310</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CYM58</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Cymbastela coralliophila (Porifera): 100mg/L; Week4</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591320">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591320</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436890</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CYM58</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987311" alias="T_CYM59">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987311</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CYM59</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Cymbastela coralliophila (Porifera): 100mg/L; Week4</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591321">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591321</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436891</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CYM59</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987312" alias="T_CYM60">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987312</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CYM60</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Cymbastela coralliophila (Porifera): 100mg/L; Week4</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591322">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591322</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436892</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CYM60</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987313" alias="T_CYM61">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987313</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CYM61</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Cymbastela coralliophila (Porifera): 100mg/L; Week4</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591323">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591323</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436893</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CYM61</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987314" alias="T_CYM62">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987314</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CYM62</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Cymbastela coralliophila (Porifera): 100mg/L; Week4</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591324">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591324</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436894</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CYM62</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987315" alias="T_CAR19">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987315</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CAR19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Carteriospongia foliascens (Porifera): 0mg/L; Week4</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591326">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591326</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436751</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CAR19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987316" alias="T_STY1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987316</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_STY1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Stylissa flabelliformis (Porifera): Field Control</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591325">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591325</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436895</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_STY1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987317" alias="T_STY2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987317</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_STY2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Stylissa flabelliformis (Porifera): Field Control</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591327">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591327</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436896</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_STY2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987318" alias="T_STY3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987318</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_STY3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Stylissa flabelliformis (Porifera): Field Control</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591328">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591328</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436897</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_STY3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987319" alias="T_STY4">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987319</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_STY4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Stylissa flabelliformis (Porifera): Field Control</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591329">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591329</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436898</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_STY4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987320" alias="T_STY5">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987320</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_STY5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Stylissa flabelliformis (Porifera): Field Control</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591330">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591330</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436899</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_STY5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987321" alias="T_STY7">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987321</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_STY7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Stylissa flabelliformis (Porifera): Time0 Control</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591331">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591331</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436900</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_STY7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987322" alias="T_STY8">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987322</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_STY8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Stylissa flabelliformis (Porifera): Time0 Control</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591332">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591332</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436901</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_STY8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987323" alias="T_STY9">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987323</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_STY9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Stylissa flabelliformis (Porifera): Time0 Control</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591333">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591333</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436902</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_STY9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987324" alias="T_STY10">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987324</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_STY10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Stylissa flabelliformis (Porifera): Time0 Control</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591334">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591334</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436903</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_STY10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987325" alias="T_STY11">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987325</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_STY11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Stylissa flabelliformis (Porifera): Time0 Control</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591335">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591335</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436904</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_STY11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987326" alias="T_CAR20">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987326</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CAR20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Carteriospongia foliascens (Porifera): 0mg/L; Week4</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591336">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591336</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436752</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CAR20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987327" alias="T_STY13">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987327</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_STY13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Stylissa flabelliformis (Porifera): 0mg/L; Recovery</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591337">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591337</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436905</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_STY13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987328" alias="T_STY14">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987328</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_STY14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Stylissa flabelliformis (Porifera): 0mg/L; Recovery</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591338">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591338</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436906</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_STY14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987329" alias="T_STY15">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987329</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_STY15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Stylissa flabelliformis (Porifera): 0mg/L; Recovery</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591339">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591339</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436907</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_STY15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987330" alias="T_STY16">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987330</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_STY16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Stylissa flabelliformis (Porifera): 0mg/L; Recovery</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591340">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591340</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436908</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_STY16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987331" alias="T_STY17">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987331</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_STY17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Stylissa flabelliformis (Porifera): 0mg/L; Recovery</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591341">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591341</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436909</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_STY17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987332" alias="T_STY18">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987332</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_STY18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Stylissa flabelliformis (Porifera): 0mg/L; Week4</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591343">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591343</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436910</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_STY18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987333" alias="T_STY19">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987333</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_STY19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Stylissa flabelliformis (Porifera): 0mg/L; Week4</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591342">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591342</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436911</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_STY19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987334" alias="T_STY20">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987334</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_STY20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Stylissa flabelliformis (Porifera): 0mg/L; Week4</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591344">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591344</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436912</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_STY20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987335" alias="T_STY21">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987335</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_STY21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Stylissa flabelliformis (Porifera): 0mg/L; Week4</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591345">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591345</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436913</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_STY21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987336" alias="T_STY22">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987336</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_STY22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Stylissa flabelliformis (Porifera): 0mg/L; Week4</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591346">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591346</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436914</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_STY22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987337" alias="T_CAR21">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987337</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CAR21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Carteriospongia foliascens (Porifera): 0mg/L; Week4</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591347">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591347</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436753</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CAR21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987338" alias="T_STY43">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987338</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_STY43</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Stylissa flabelliformis (Porifera): 30mg/L; Recovery</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591348">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591348</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436915</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_STY43</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987339" alias="T_STY44">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987339</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_STY44</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Stylissa flabelliformis (Porifera): 30mg/L; Recovery</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591349">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591349</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436916</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_STY44</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987340" alias="T_STY45">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987340</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_STY45</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Stylissa flabelliformis (Porifera): 30mg/L; Recovery</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591350">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591350</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436917</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_STY45</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987341" alias="T_STY46">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987341</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_STY46</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Stylissa flabelliformis (Porifera): 30mg/L; Recovery</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591351">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591351</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436918</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_STY46</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987342" alias="T_STY47">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987342</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_STY47</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Stylissa flabelliformis (Porifera): 30mg/L; Recovery</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591352">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591352</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436919</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_STY47</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987343" alias="T_STY48">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987343</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_STY48</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Stylissa flabelliformis (Porifera): 30mg/L; Week4</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591353">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591353</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436920</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_STY48</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987344" alias="T_STY49">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987344</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_STY49</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Stylissa flabelliformis (Porifera): 30mg/L; Week4</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591354">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591354</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436921</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_STY49</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987345" alias="T_STY50">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987345</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_STY50</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Stylissa flabelliformis (Porifera): 30mg/L; Week4</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591355">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591355</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436922</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_STY50</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987346" alias="T_STY51">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987346</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_STY51</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Stylissa flabelliformis (Porifera): 30mg/L; Week4</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591356">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591356</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436923</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_STY51</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987347" alias="T_STY52">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987347</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_STY52</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Stylissa flabelliformis (Porifera): 30mg/L; Week4</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591357">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591357</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436924</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_STY52</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987348" alias="T_CAR22">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987348</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CAR22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Carteriospongia foliascens (Porifera): 0mg/L; Week4</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591358">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591358</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436754</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CAR22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987349" alias="T_STY53">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987349</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_STY53</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Stylissa flabelliformis (Porifera): 100mg/L; Recovery</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591359">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591359</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436925</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_STY53</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987350" alias="T_STY54">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987350</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_STY54</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Stylissa flabelliformis (Porifera): 100mg/L; Recovery</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591360">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591360</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436926</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_STY54</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987351" alias="T_STY55">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987351</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_STY55</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Stylissa flabelliformis (Porifera): 100mg/L; Recovery</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591361">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591361</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436927</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_STY55</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987352" alias="T_STY56">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987352</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_STY56</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Stylissa flabelliformis (Porifera): 100mg/L; Recovery</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591362">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591362</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436928</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_STY56</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987353" alias="T_STY57">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987353</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_STY57</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Stylissa flabelliformis (Porifera): 100mg/L; Recovery</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591363">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591363</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436929</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_STY57</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987354" alias="T_STY58">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987354</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_STY58</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Stylissa flabelliformis (Porifera): 100mg/L; Week4</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591364">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591364</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436930</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_STY58</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987355" alias="T_STY59">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987355</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_STY59</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Stylissa flabelliformis (Porifera): 100mg/L; Week4</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591365">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591365</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436931</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_STY59</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987356" alias="T_STY60">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987356</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_STY60</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Stylissa flabelliformis (Porifera): 100mg/L; Week4</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591366">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591366</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436932</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_STY60</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987357" alias="T_STY61">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987357</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_STY61</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Stylissa flabelliformis (Porifera): 100mg/L; Week4</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591367">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591367</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436933</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_STY61</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987358" alias="T_STY62">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987358</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_STY62</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Stylissa flabelliformis (Porifera): 100mg/L; Week4</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591368">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591368</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436934</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_STY62</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987359" alias="T_CAR3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987359</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CAR3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Carteriospongia foliascens (Porifera): Field Control</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591369">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591369</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436737</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CAR3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987360" alias="T_CAR43">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987360</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CAR43</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Carteriospongia foliascens (Porifera): 30mg/L; Recovery</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591370">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591370</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436755</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CAR43</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987361" alias="T_SW_T4">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987361</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_SW_T4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of seawater (environmental control): 100 mg/L</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Microbial communities in seawater were collected by passing 1L of seawater through 0.2 µm Sterivex filters and DNA was extracted from the filters. Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591371">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591371</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436935</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_SW_T4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987362" alias="T_SW_T5">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987362</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_SW_T5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of seawater (environmental control): 0 mg/L</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Microbial communities in seawater were collected by passing 1L of seawater through 0.2 µm Sterivex filters and DNA was extracted from the filters. Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591372">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591372</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436936</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_SW_T5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987363" alias="T_SW_T7">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987363</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_SW_T7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of seawater (environmental control): 30 mg/L</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Microbial communities in seawater were collected by passing 1L of seawater through 0.2 µm Sterivex filters and DNA was extracted from the filters. Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591373">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591373</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436937</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_SW_T7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987364" alias="T_SW_T9">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987364</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_SW_T9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of seawater (environmental control): 0 mg/L</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Microbial communities in seawater were collected by passing 1L of seawater through 0.2 µm Sterivex filters and DNA was extracted from the filters. Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591374">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591374</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436938</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_SW_T9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987365" alias="T_SW_T10">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987365</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_SW_T10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of seawater (environmental control): 30 mg/L</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Microbial communities in seawater were collected by passing 1L of seawater through 0.2 µm Sterivex filters and DNA was extracted from the filters. Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591375">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591375</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436939</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_SW_T10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987366" alias="T_SW_12">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987366</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_SW_12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of seawater (environmental control): 100 mg/L</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Microbial communities in seawater were collected by passing 1L of seawater through 0.2 µm Sterivex filters and DNA was extracted from the filters. Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591376">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591376</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436940</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_SW_12</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987367" alias="T_SW_T15">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987367</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_SW_T15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of seawater (environmental control): 0 mg/L</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Microbial communities in seawater were collected by passing 1L of seawater through 0.2 µm Sterivex filters and DNA was extracted from the filters. Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591377">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591377</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436941</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_SW_T15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987368" alias="T_SW_T17">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987368</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_SW_T17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of seawater (environmental control): 30 mg/L</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Microbial communities in seawater were collected by passing 1L of seawater through 0.2 µm Sterivex filters and DNA was extracted from the filters. Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591378">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591378</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436942</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_SW_T17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987369" alias="T_SW_18">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987369</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_SW_18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of seawater (environmental control): 100 mg/L</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Microbial communities in seawater were collected by passing 1L of seawater through 0.2 µm Sterivex filters and DNA was extracted from the filters. Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591379">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591379</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436943</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_SW_18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987370" alias="T_CAR44">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987370</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CAR44</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Carteriospongia foliascens (Porifera): 30mg/L; Recovery</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591380">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591380</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436756</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CAR44</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987371" alias="T_CAR45">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987371</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CAR45</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Carteriospongia foliascens (Porifera): 30mg/L; Recovery</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591381">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591381</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436757</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CAR45</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987372" alias="T_CAR46">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987372</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CAR46</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Carteriospongia foliascens (Porifera): 30mg/L; Recovery</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591382">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591382</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436758</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CAR46</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987373" alias="T_CAR47">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987373</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CAR47</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Carteriospongia foliascens (Porifera): 30mg/L; Recovery</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591383">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591383</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436759</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CAR47</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987374" alias="T_CAR48">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987374</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CAR48</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Carteriospongia foliascens (Porifera): 30mg/L; Week4</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591384">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591384</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436760</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CAR48</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987375" alias="T_CAR49">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987375</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CAR49</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Carteriospongia foliascens (Porifera): 30mg/L; Week4</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591385">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591385</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436761</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CAR49</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987376" alias="T_CAR50">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987376</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CAR50</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Carteriospongia foliascens (Porifera): 30mg/L; Week4</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591386">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591386</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436762</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CAR50</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987377" alias="T_CAR51">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987377</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CAR51</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Carteriospongia foliascens (Porifera): 30mg/L; Week4</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591387">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591387</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436763</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CAR51</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987378" alias="T_CAR52">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987378</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CAR52</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Carteriospongia foliascens (Porifera): 30mg/L; Week4</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591388">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591388</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436764</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CAR52</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987379" alias="T_CAR4">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987379</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CAR4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Carteriospongia foliascens (Porifera): Field Control</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591389">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591389</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436738</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CAR4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987380" alias="T_CAR53">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987380</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CAR53</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Carteriospongia foliascens (Porifera): 100mg/L; Recovery</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591390">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591390</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436765</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CAR53</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987381" alias="T_CAR54">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987381</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CAR54</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Carteriospongia foliascens (Porifera): 100mg/L; Recovery</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591391">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591391</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436766</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CAR54</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987382" alias="T_CAR55">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987382</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CAR55</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Carteriospongia foliascens (Porifera): 100mg/L; Recovery</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591392">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591392</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436767</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CAR55</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987383" alias="T_CAR56">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987383</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CAR56</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Carteriospongia foliascens (Porifera): 100mg/L; Recovery</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591393">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591393</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436768</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CAR56</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987384" alias="T_CAR57">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987384</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CAR57</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Carteriospongia foliascens (Porifera): 100mg/L; Recovery</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591394">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591394</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436769</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CAR57</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987385" alias="T_CAR58">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987385</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CAR58</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Carteriospongia foliascens (Porifera): 100mg/L; Week4</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591395">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591395</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436770</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CAR58</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987386" alias="T_CAR59">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987386</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CAR59</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Carteriospongia foliascens (Porifera): 100mg/L; Week4</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591396">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591396</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436771</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CAR59</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987387" alias="T_CAR60">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987387</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CAR60</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Carteriospongia foliascens (Porifera): 100mg/L; Week4</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591397">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591397</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436772</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CAR60</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987388" alias="T_CAR61">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987388</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CAR61</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Carteriospongia foliascens (Porifera): 100mg/L; Week4</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591398">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591398</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436773</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CAR61</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987389" alias="T_CAR62">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987389</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CAR62</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Carteriospongia foliascens (Porifera): 100mg/L; Week4</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591399">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591399</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436774</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CAR62</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987390" alias="T_CAR5">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987390</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CAR5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Carteriospongia foliascens (Porifera): Field Control</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591400">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591400</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436739</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CAR5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987391" alias="T_CLI1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987391</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CLI1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Cliona orientalis (Porifera): Field Control</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591401">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591401</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436775</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CLI1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987392" alias="T_CLI2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987392</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CLI2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Cliona orientalis (Porifera): Field Control</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591402">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591402</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436776</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CLI2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987393" alias="T_CLI3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987393</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CLI3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Cliona orientalis (Porifera): Field Control</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591403">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591403</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436777</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CLI3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987394" alias="T_CLI4">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987394</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CLI4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Cliona orientalis (Porifera): Field Control</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591404">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591404</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436778</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CLI4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987395" alias="T_CLI5">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987395</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CLI5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Cliona orientalis (Porifera): Field Control</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591405">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591405</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436779</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CLI5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987396" alias="T_CLI7">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987396</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CLI7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Cliona orientalis (Porifera): Time0 Control</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591406">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591406</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436780</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CLI7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987397" alias="T_CLI8">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987397</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CLI8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Cliona orientalis (Porifera): Time0 Control</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591407">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591407</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436781</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CLI8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987398" alias="T_CLI9">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987398</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CLI9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Cliona orientalis (Porifera): Time0 Control</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591408">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591408</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436782</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CLI9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987399" alias="T_CLI10">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987399</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CLI10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Cliona orientalis (Porifera): Time0 Control</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591409">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591409</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436783</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CLI10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987400" alias="T_CLI11">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987400</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CLI11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Cliona orientalis (Porifera): Time0 Control</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591410">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591410</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436784</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CLI11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987401" alias="T_CAR7">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987401</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CAR7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Carteriospongia foliascens (Porifera): Time0 Control</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591411">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591411</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436740</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CAR7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987402" alias="T_CLI13">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987402</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CLI13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Cliona orientalis (Porifera): 0mg/L; Recovery</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591413">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591413</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436785</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CLI13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987403" alias="T_CLI14">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987403</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CLI14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Cliona orientalis (Porifera): 0mg/L; Recovery</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591412">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591412</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436786</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CLI14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987404" alias="T_CLI15">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987404</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CLI15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Cliona orientalis (Porifera): 0mg/L; Recovery</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591414">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591414</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436787</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CLI15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987405" alias="T_CLI16">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987405</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CLI16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Cliona orientalis (Porifera): 0mg/L; Recovery</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591415">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591415</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436788</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CLI16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987406" alias="T_CLI17">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987406</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CLI17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Cliona orientalis (Porifera): 0mg/L; Recovery</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591416">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591416</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436789</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CLI17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987407" alias="T_CLI18">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987407</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CLI18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Cliona orientalis (Porifera): 0mg/L; Week4</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591417">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591417</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436790</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CLI18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987408" alias="T_CLI19">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987408</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CLI19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Cliona orientalis (Porifera): 0mg/L; Week4</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591418">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591418</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436791</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CLI19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987409" alias="T_CLI20">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987409</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CLI20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Cliona orientalis (Porifera): 0mg/L; Week4</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591419">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591419</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436792</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CLI20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987410" alias="T_CLI21">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987410</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CLI21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Cliona orientalis (Porifera): 0mg/L; Week4</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591420">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591420</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436793</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CLI21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987411" alias="T_CLI22">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987411</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CLI22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Cliona orientalis (Porifera): 0mg/L; Week4</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591421">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591421</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436794</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CLI22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987412" alias="T_CAR8">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987412</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CAR8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Carteriospongia foliascens (Porifera): Time0 Control</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591422">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591422</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436741</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CAR8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987413" alias="T_CLI43">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987413</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CLI43</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Cliona orientalis (Porifera): 30mg/L; Recovery</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591423">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591423</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436795</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CLI43</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987414" alias="T_CLI44">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987414</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CLI44</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Cliona orientalis (Porifera): 30mg/L; Recovery</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591424">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591424</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436796</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CLI44</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987415" alias="T_CLI45">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987415</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CLI45</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Cliona orientalis (Porifera): 30mg/L; Recovery</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591425">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591425</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436797</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CLI45</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987416" alias="T_CLI46">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987416</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CLI46</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Cliona orientalis (Porifera): 30mg/L; Recovery</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591426">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591426</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436798</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CLI46</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987417" alias="T_CLI47">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987417</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CLI47</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Cliona orientalis (Porifera): 30mg/L; Recovery</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591427">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591427</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436799</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CLI47</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987418" alias="T_CLI48">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987418</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CLI48</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Cliona orientalis (Porifera): 30mg/L; Week4</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591428">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591428</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436800</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CLI48</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987419" alias="T_CLI49">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987419</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CLI49</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Cliona orientalis (Porifera): 30mg/L; Week4</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591429">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591429</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436801</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CLI49</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987420" alias="T_CLI50">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987420</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CLI50</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Cliona orientalis (Porifera): 30mg/L; Week4</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591431">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591431</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436802</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CLI50</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987421" alias="T_CLI51">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987421</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CLI51</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Cliona orientalis (Porifera): 30mg/L; Week4</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591430">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591430</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436803</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CLI51</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987422" alias="T_CLI52">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987422</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CLI52</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Cliona orientalis (Porifera): 30mg/L; Week4</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591432">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591432</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436804</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CLI52</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987423" alias="T_CAR9">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987423</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CAR9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Carteriospongia foliascens (Porifera): Time0 Control</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591433">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591433</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436742</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CAR9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987424" alias="T_CLI53">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987424</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CLI53</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Cliona orientalis (Porifera): 100mg/L; Recovery</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591434">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591434</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436805</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CLI53</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987425" alias="T_CLI54">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987425</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CLI54</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Cliona orientalis (Porifera): 100mg/L; Recovery</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591435">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591435</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436806</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CLI54</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987426" alias="T_CLI55">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987426</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CLI55</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Cliona orientalis (Porifera): 100mg/L; Recovery</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591436">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591436</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436807</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CLI55</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987427" alias="T_CLI56">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987427</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CLI56</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Cliona orientalis (Porifera): 100mg/L; Recovery</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591437">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591437</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436808</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CLI56</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987428" alias="T_CLI57">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987428</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CLI57</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Cliona orientalis (Porifera): 100mg/L; Recovery</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591438">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591438</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436809</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CLI57</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987429" alias="T_CLI58">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987429</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CLI58</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Cliona orientalis (Porifera): 100mg/L; Week4</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591439">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591439</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436810</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CLI58</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987430" alias="T_CLI59">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987430</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CLI59</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Cliona orientalis (Porifera): 100mg/L; Week4</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591440">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591440</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436811</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CLI59</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987431" alias="T_CLI60">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987431</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CLI60</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Cliona orientalis (Porifera): 100mg/L; Week4</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591441">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591441</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436812</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CLI60</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987432" alias="T_CLI61">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987432</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CLI61</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Cliona orientalis (Porifera): 100mg/L; Week4</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591442">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591442</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436813</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CLI61</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987433" alias="T_CLI62">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987433</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CLI62</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Cliona orientalis (Porifera): 100mg/L; Week4</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591443">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591443</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436814</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CLI62</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987434" alias="T_CAR10">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987434</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CAR10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Carteriospongia foliascens (Porifera): Time0 Control</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591445">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591445</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436743</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CAR10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987435" alias="T_COS1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987435</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_COS1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Coscinoderma matthewsi (Porifera): Field Control</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591444">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591444</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436815</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_COS1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987436" alias="T_COS2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987436</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_COS2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Coscinoderma matthewsi (Porifera): Field Control</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591446">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591446</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436816</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_COS2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987437" alias="T_COS3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987437</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_COS3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Coscinoderma matthewsi (Porifera): Field Control</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591447">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591447</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436817</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_COS3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987438" alias="T_COS4">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987438</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_COS4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Coscinoderma matthewsi (Porifera): Field Control</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591448">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591448</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436818</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_COS4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987439" alias="T_COS5">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987439</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_COS5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Coscinoderma matthewsi (Porifera): Field Control</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591449">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591449</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436819</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_COS5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987440" alias="T_COS7">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987440</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_COS7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Coscinoderma matthewsi (Porifera): Time0 Control</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591450">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591450</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436820</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_COS7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987441" alias="T_COS8">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987441</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_COS8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Coscinoderma matthewsi (Porifera): Time0 Control</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591452">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591452</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436821</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_COS8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987442" alias="T_COS9">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987442</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_COS9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Coscinoderma matthewsi (Porifera): Time0 Control</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591451">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591451</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436822</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_COS9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987443" alias="T_COS10">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987443</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_COS10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Coscinoderma matthewsi (Porifera): Time0 Control</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591453">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591453</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436823</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_COS10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987444" alias="T_COS11">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987444</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_COS11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Coscinoderma matthewsi (Porifera): Time0 Control</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591454">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591454</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436824</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_COS11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987445" alias="T_CAR11">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987445</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_CAR11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Carteriospongia foliascens (Porifera): Time0 Control</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591455">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591455</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436744</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_CAR11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987446" alias="T_COS13">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987446</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_COS13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Coscinoderma matthewsi (Porifera): 0mg/L; Recovery</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591456">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591456</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436825</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_COS13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987447" alias="T_COS14">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987447</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_COS14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Coscinoderma matthewsi (Porifera): 0mg/L; Recovery</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591457">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591457</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436826</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_COS14</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987448" alias="T_COS15">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987448</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_COS15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Coscinoderma matthewsi (Porifera): 0mg/L; Recovery</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591458">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591458</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436827</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_COS15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987449" alias="T_COS16">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987449</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_COS16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Coscinoderma matthewsi (Porifera): 0mg/L; Recovery</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591459">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591459</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436828</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_COS16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987450" alias="T_COS17">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987450</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_COS17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Coscinoderma matthewsi (Porifera): 0mg/L; Recovery</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591460">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591460</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436829</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_COS17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987451" alias="T_COS18">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987451</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_COS18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Coscinoderma matthewsi (Porifera): 0mg/L; Week4</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591461">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591461</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436830</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_COS18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987452" alias="T_COS19">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987452</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_COS19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Coscinoderma matthewsi (Porifera): 0mg/L; Week4</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591462">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591462</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436831</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_COS19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987453" alias="T_COS20">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987453</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_COS20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Coscinoderma matthewsi (Porifera): 0mg/L; Week4</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591464">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591464</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436832</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_COS20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987454" alias="T_COS21">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987454</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_COS21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Coscinoderma matthewsi (Porifera): 0mg/L; Week4</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591463">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591463</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436833</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_COS21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1987455" alias="T_COS22">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1987455</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1720495">T_COS22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>16S of Coscinoderma matthewsi (Porifera): 0mg/L; Week4</TITLE>
    <STUDY_REF accession="SRP080228">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP080228</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA330753</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA  extracted from ~0.2 g of sponge tissue using the PowerPlant® Pro DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA). Extracted DNA was shipped to the Australian Centre for Ecogenomics (St. Lucia, QLD, Australia) for sequencing of the 16S rRNA gene using standard procedures. Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f – 806r and sequenced using the HiSeq2500 platform with the V2 chemistry (2 x 250 bp) (Illumina).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1591465">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1591465</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05436834</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>T_COS22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>METAGENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
