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        <gco:CharacterString>Dataset Description: &amp;lt;p&amp;gt;See &amp;quot;Data&amp;amp;nbsp;Files&amp;quot; section for access to download the data and analysis code&amp;amp;nbsp;&amp;quot;Ashworth_data_and_analysis.zip&amp;quot;.&amp;amp;nbsp; The sample information and genetic&amp;amp;nbsp;accession identifiers are&amp;amp;nbsp;available as a data table from this page.&amp;lt;/p&amp;gt; Methods and Sampling: &amp;lt;p&amp;gt;&amp;lt;strong&amp;gt;Location:&amp;amp;nbsp;&amp;lt;/strong&amp;gt;&amp;lt;br /&amp;gt;
&amp;lt;br /&amp;gt;
Lab work performed at University of Alabama at Birmingham and University of Texas at Austin; Samples collected from Guam, California, and Gulf of Mexico.&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;&amp;lt;strong&amp;gt;Sampling and analytical procedures:&amp;amp;nbsp;&amp;lt;/strong&amp;gt;&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt; Cultures were obtained from sites in Guam, California, and the Gulf of Mexico near Florida. Cells were isolated from collections made primarily by plankton net with 20 m mesh or by collection of the top millimeters of sediment from the benthos. Individual cells were isolated by glass Pasteur pipet (Andersen) into 15x100 mm glass test tubes in approximately 12 mL of liquid f/2 medium with double the normal concentration of silica (Guillard, Andersen) at a salinity of 32-35 ppt. The f/2 base was seawater collected from the Texas coast of the Gulf of Mexico and passed through a 0.22 um filter. Isolates were maintained under natural light from a north facing window between 20-24oC, or in a Percival growth chamber on a 12:12 light:dark cycle at 27oC in the case of the isolates from Guam. Once unialgal growth was confirmed by microscopy, strains were maintained in triplicate with cells (approximately 0.25 mL) from one tube transferred to three fresh media tubes every 3-4 months.&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;During the strain transfer cycle, one replicate tube was harvested by Pasteur pipet into a 1.5 mL microcentrifuge tube and centrifuged in an Eppendorf 5414 C microcentrifuge at 8,000 rpm for 10 minutes. Liquid media was decanted off the pellet, and the pellet was stored at -80oC until DNA extraction. DNA was extracted from the pellets using a MoBio Powersoil DNA kit, following the manufacturers protocol.&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;The V4 region of the bacterial 16S rRNA gene was amplified using bar-coded PCR primers (Caporaso), purified by gel electrophoresis, and then sequenced using the Illumina MiSeq platform. &amp;amp;nbsp;Quality control and sequence analysis was performed in mothur according to the mothur MiSeq SOP protocol (Schlosss, Kozich).&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;Sequence data is available from the NCBI SRA archive, BioProject PRJNA706454.&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;&amp;lt;br /&amp;gt;
&amp;lt;strong&amp;gt;Species List (ScientificName,AphiaID)&amp;lt;/strong&amp;gt;&amp;lt;br /&amp;gt;
&amp;lt;br /&amp;gt;
Astrosyne radiata,837899&amp;lt;br /&amp;gt;
Roundia cardiophora,627356&amp;lt;br /&amp;gt;
Florella pascuensis,646734&amp;lt;br /&amp;gt;
Triceratium dubium,418600&amp;lt;br /&amp;gt;
Striatella unipunctata,149177&amp;lt;br /&amp;gt;
Hanicella moenia,842549&amp;lt;br /&amp;gt;
Paralia longispina,708079&amp;lt;br /&amp;gt;
Astrosyne radiata,837899&amp;lt;br /&amp;gt;
Neosynedra provincialis,175369&amp;lt;br /&amp;gt;
Leptocylindrus danicus,149106&amp;lt;/p&amp;gt;</gco:CharacterString>
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&amp;lt;br /&amp;gt;
Lab work performed at University of Alabama at Birmingham and University of Texas at Austin; Samples collected from Guam, California, and Gulf of Mexico.&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;&amp;lt;strong&amp;gt;Sampling and analytical procedures:&amp;amp;nbsp;&amp;lt;/strong&amp;gt;&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt; Cultures were obtained from sites in Guam, California, and the Gulf of Mexico near Florida. Cells were isolated from collections made primarily by plankton net with 20 m mesh or by collection of the top millimeters of sediment from the benthos. Individual cells were isolated by glass Pasteur pipet (Andersen) into 15x100 mm glass test tubes in approximately 12 mL of liquid f/2 medium with double the normal concentration of silica (Guillard, Andersen) at a salinity of 32-35 ppt. The f/2 base was seawater collected from the Texas coast of the Gulf of Mexico and passed through a 0.22 um filter. Isolates were maintained under natural light from a north facing window between 20-24oC, or in a Percival growth chamber on a 12:12 light:dark cycle at 27oC in the case of the isolates from Guam. Once unialgal growth was confirmed by microscopy, strains were maintained in triplicate with cells (approximately 0.25 mL) from one tube transferred to three fresh media tubes every 3-4 months.&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;During the strain transfer cycle, one replicate tube was harvested by Pasteur pipet into a 1.5 mL microcentrifuge tube and centrifuged in an Eppendorf 5414 C microcentrifuge at 8,000 rpm for 10 minutes. Liquid media was decanted off the pellet, and the pellet was stored at -80oC until DNA extraction. DNA was extracted from the pellets using a MoBio Powersoil DNA kit, following the manufacturers protocol.&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;The V4 region of the bacterial 16S rRNA gene was amplified using bar-coded PCR primers (Caporaso), purified by gel electrophoresis, and then sequenced using the Illumina MiSeq platform. &amp;amp;nbsp;Quality control and sequence analysis was performed in mothur according to the mothur MiSeq SOP protocol (Schlosss, Kozich).&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;Sequence data is available from the NCBI SRA archive, BioProject PRJNA706454.&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;&amp;lt;br /&amp;gt;
&amp;lt;strong&amp;gt;Species List (ScientificName,AphiaID)&amp;lt;/strong&amp;gt;&amp;lt;br /&amp;gt;
&amp;lt;br /&amp;gt;
Astrosyne radiata,837899&amp;lt;br /&amp;gt;
Roundia cardiophora,627356&amp;lt;br /&amp;gt;
Florella pascuensis,646734&amp;lt;br /&amp;gt;
Triceratium dubium,418600&amp;lt;br /&amp;gt;
Striatella unipunctata,149177&amp;lt;br /&amp;gt;
Hanicella moenia,842549&amp;lt;br /&amp;gt;
Paralia longispina,708079&amp;lt;br /&amp;gt;
Astrosyne radiata,837899&amp;lt;br /&amp;gt;
Neosynedra provincialis,175369&amp;lt;br /&amp;gt;
Leptocylindrus danicus,149106&amp;lt;/p&amp;gt;</gco:CharacterString>
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&amp;lt;p&amp;gt;mothur version &amp;amp;nbsp;1.42.3&amp;lt;br /&amp;gt;
&amp;lt;br /&amp;gt;
BCO-DMO Data Manager processing notes:&amp;lt;br /&amp;gt;
* Species names in file axes.csv run through the World Register of Marine Species (WoRMS) taxa match tool to check taxonomic names.&amp;amp;nbsp; All names matched accepted names exactly as of 2021-07-15.&amp;amp;nbsp; Unique species list with associated AphiaIDs added to the metadata.&amp;lt;br /&amp;gt;
* Sample collection information and accession numbers at NCBI extracted using the NCBI Run Selector.&amp;amp;nbsp; Sample information imported into the BCO-DMO data system.&amp;amp;nbsp;&amp;lt;br /&amp;gt;
* Latitude and longitude split into individual columns and converted to decimal degrees.&amp;amp;nbsp; e.g. lat_lon &amp;quot;24.84 N 80.78 W&amp;quot; -&amp;amp;gt; lat: 24.84, lon: -80.78&amp;lt;br /&amp;gt;
* After email correspondence about a coordinate outlier, the latitude for &amp;quot;USA: San Pedro California, kelp bed&amp;quot; was changed from 38.71 to&amp;amp;nbsp;33.71 after the submitters double-checked their notes.&amp;lt;/p&amp;gt;</gco:CharacterString>
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            <gmd:MD_Identifier>
              <gmd:code>
                <gmx:Anchor xlink:href="http://lod.bco-dmo.org/id/instrument/629890.rdf" xlink:title="Centrifuge" xlink:actuate="onRequest">Eppendorf 5414 C microcentrifuge</gmx:Anchor>
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