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            <gco:CharacterString>Cite this dataset as: Worden, A. Z. (2011) Links to accessions for 18S rDNA, chloroplast and metagenomics (picoeukaryote) data from multiple cruises from the Sargasso Sea and CalCOFI line 67 from 2001-2009 (PHYTO_GENOME project). Biological and Chemical Oceanography Data Management Office (BCO-DMO). (Version 18 January 2011) Version Date 2011-01-18 [if applicable, indicate subset used]. http://lod.bco-dmo.org/id/dataset/3373 [access date]</gco:CharacterString>
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        <gco:CharacterString>Links to Accessions for 18S rDNA , chloroplast and metagenomics data Dataset Description: &amp;lt;p&amp;gt;Accessions for 18S rDNA , chloroplast and metagenomics data&amp;lt;br /&amp;gt;
&amp;lt;br /&amp;gt;
Biliphyte sequences from this study have been deposited in GenBank under Accession No. EU368003-EU368039&amp;lt;br /&amp;gt;
&amp;lt;br /&amp;gt;
Cuvelier ML, Ortiz A, Kim E, Moehlig H, Richardson DE, Heidelberg JF, Archibald JM, Worden AZ (2008).&amp;lt;br /&amp;gt;
Widespread distribution of a unique marine protistan lineage. Environmental Microbiology. Vol. 10:1621-1634.&amp;lt;br /&amp;gt;
&amp;lt;br /&amp;gt;
Prymnesiophyte sequences from this study have been deposited in GenBank under Accession Nos.&amp;lt;br /&amp;gt;
HM581528-HM581638 and HM565909-HM565914. Other scaffolds with predicted genes from this Whole&amp;lt;br /&amp;gt;
Genome Shotgun/454 project have been deposited at DNA Data Bank of Japan/European Molecular Biology&amp;lt;br /&amp;gt;
Laboratory/GenBank under the accession no. AEAR00000000. The version described in this paper is&amp;lt;br /&amp;gt;
the first version, AEAR01000000.&amp;lt;br /&amp;gt;
&amp;lt;br /&amp;gt;
Cuvelier ML, Allen* AE, Monier* A, McCrow JP, Messie M, Tringe SG, Woyke T, Welsh RM, Ishoey T,&amp;lt;br /&amp;gt;
Lee JH, Binder BJ, DuPont CL, Latasa M, Guigand C, Buck KR, Hilton J, Thiagarajan M, Caler E,&amp;lt;br /&amp;gt;
Read B, Lasken RS, Chavez FP &amp;amp;amp; AZ Worden (2010). Targeted metagenomics and ecology of globally&amp;lt;br /&amp;gt;
important uncultured eukaryotic phytoplankton. Proceedings of the National Academy of Sciences USA.&amp;lt;br /&amp;gt;
&amp;lt;br /&amp;gt;
Alveolate sequences from this study have been deposited in GenBank under:&amp;lt;br /&amp;gt;
EU818567-EU818691, EU836584-EU836597, EU818578-EU818566, EU817966-EU818077,&amp;lt;br /&amp;gt;
EU836613-EU836615; EU817882-EU817965; EU836616-EU816617&amp;lt;br /&amp;gt;
&amp;lt;br /&amp;gt;
Guillou L, Viprey M, Chambouvet A, Welsh RM, Kirkham AR, Massana R, Scanlan DJ and&amp;amp;nbsp;AZ Worden (2008).&amp;lt;br /&amp;gt;
Widespread occurrence and genetic diversity of marine parasitoids belonging to Syndiniales (Alveolata).&amp;lt;br /&amp;gt;
Environmental Microbiology. DOI: 10.1111/j.1462-2920.2008.01731.x&amp;lt;/p&amp;gt; Methods and Sampling: &amp;lt;p&amp;gt;Samples were typically taken at the surface and deep chlorophyll maximum using a niskin rosette, all contextual data available (typically temperature and salinity) was deposited with the GenBank Submission for each sequence.&amp;lt;br /&amp;gt;
&amp;lt;br /&amp;gt;
&amp;lt;u&amp;gt;Field sites and sample collection&amp;lt;/u&amp;gt;&amp;lt;br /&amp;gt;
Five cruises were conducted, two transects from coastal New England to the BATS site (R/V Endeavor cruise EN351 and R/V Oceanus cruise OC413) and three transects across the Florida Straits (R/V Walton Smith cruises WS0503, WS0518, WS0528) with characteristics as in Table 1. Samples were collected in surface and DCM waters using a Sea-Bird Niskin Rosette equipped with standard CTD and PAR detectors (see also below). For DNA extraction samples, 1 l of seawater was gravity filtered through 2 um pore size filters (GE Osmonics, Minnetonka, MN, USA) and then onto a 0.45 um pore size (2001) or 0.2 um pore size (2005) Supor filter (Pall Gelman, Ann Arbor, MI, USA) using vacuum. For FISH samples whole seawater (no size fractionation) was preserved with 1% paraformaldahyde (final concentration) for at least 1 h in the dark at 4&amp;amp;deg;C. For each replicate, volumes of 180 ml or more of seawater were gently filtered onto a 25 mm, 0.2 um Anodisc filter (Whatman, Maidstone, England). The filters were then subjected to an ethanol dehydration series at 50%, 80%, 100% (diluted in sterile, 18.2 &amp;amp;deg; H2O) for 3 min each and stored at -80&amp;amp;deg;C. Flow cytometry samples were preserved with 0.25% (final concentration) fresh electron microscopy grade glutaraldehyde (Tousimis, Rockville, MD, USA), flash frozen in liquid nitrogen and moved to -80&amp;amp;deg;C for long-term storage.&amp;lt;/p&amp;gt;</gco:CharacterString>
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        <gmx:Anchor xlink:href="http://lod.bco-dmo.org/id/award/54904.rdf" xlink:title="OCE-0836721" xlink:actuate="onRequest">Funding provided by NSF Division of Ocean Sciences (NSF OCE) Award Number: OCE-0836721 Award URL: https://www.nsf.gov/awardsearch/show-award?AWD_ID=0836721</gmx:Anchor>
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                <gco:CharacterString>&amp;lt;p&amp;gt;Samples were typically taken at the surface and deep chlorophyll maximum using a niskin rosette, all contextual data available (typically temperature and salinity) was deposited with the GenBank Submission for each sequence.&amp;lt;br /&amp;gt;
&amp;lt;br /&amp;gt;
&amp;lt;u&amp;gt;Field sites and sample collection&amp;lt;/u&amp;gt;&amp;lt;br /&amp;gt;
Five cruises were conducted, two transects from coastal New England to the BATS site (R/V Endeavor cruise EN351 and R/V Oceanus cruise OC413) and three transects across the Florida Straits (R/V Walton Smith cruises WS0503, WS0518, WS0528) with characteristics as in Table 1. Samples were collected in surface and DCM waters using a Sea-Bird Niskin Rosette equipped with standard CTD and PAR detectors (see also below). For DNA extraction samples, 1 l of seawater was gravity filtered through 2 um pore size filters (GE Osmonics, Minnetonka, MN, USA) and then onto a 0.45 um pore size (2001) or 0.2 um pore size (2005) Supor filter (Pall Gelman, Ann Arbor, MI, USA) using vacuum. For FISH samples whole seawater (no size fractionation) was preserved with 1% paraformaldahyde (final concentration) for at least 1 h in the dark at 4&amp;amp;deg;C. For each replicate, volumes of 180 ml or more of seawater were gently filtered onto a 25 mm, 0.2 um Anodisc filter (Whatman, Maidstone, England). The filters were then subjected to an ethanol dehydration series at 50%, 80%, 100% (diluted in sterile, 18.2 &amp;amp;deg; H2O) for 3 min each and stored at -80&amp;amp;deg;C. Flow cytometry samples were preserved with 0.25% (final concentration) fresh electron microscopy grade glutaraldehyde (Tousimis, Rockville, MD, USA), flash frozen in liquid nitrogen and moved to -80&amp;amp;deg;C for long-term storage.&amp;lt;/p&amp;gt;</gco:CharacterString>
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displacement amplification of flow cytometrically sorted&amp;lt;br /&amp;gt;
cells with subsequent Sanger and 454-FLX sequencing. See&amp;lt;br /&amp;gt;
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            <gmi:platform>
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    <gmi:citation>
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        <gmd:code>
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           xlink:title="32EV" xlink:actuate="onRequest">R/V Endeavor</gmx:Anchor>
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      </gmd:MD_Identifier>
    </gmi:identifier>
    <gmi:description>
      <gmx:Anchor xlink:href="http://lod.bco-dmo.org/id/platform/53992.rdf" xlink:title="R/V Endeavor" xlink:actuate="onRequest">vessel</gmx:Anchor>
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    <gmi:instrument gco:nilReason="unknown"/>
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