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            <gco:CharacterString>Cite this dataset as: Girguis, P. (2015) Assessments of bacterial and archaeal diversity from three distinct hydrothermal vents in the Middle Valley vent field along the Juan de Fuca Ridge from R/V Atlantis cruise AT15-67 in the Juan de Fuca Ridge in 2010. Biological and Chemical Oceanography Data Management Office (BCO-DMO). (Version 17 November 2015) Version Date 2015-11-17 [if applicable, indicate subset used]. http://lod.bco-dmo.org/id/dataset/626625 [access date]</gco:CharacterString>
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        <gco:CharacterString>Assessments of bacterial and archaeal diversity from three distinct hydrothermal vents in the Middle Valley vent field along the Juan de Fuca Ridge. Dataset Description: &amp;lt;p&amp;gt;Assessments of bacterial and archaeal diversity from three distinct hydrothermal vents in the Middle Valley vent field along the Juan de Fuca Ridge. Samples were recovered from actively venting sulfide deposits in the Middle Valley vent field along the Juan de Fuca Ridge at Needles (48.45778, -128.709), Dead Dog (48.45603,-128.71), and Chowder Hill (48.455543, -128.709) vents.&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;&amp;lt;em&amp;gt;Analysis and write up of these data can be found at:&amp;lt;/em&amp;gt;&amp;lt;br /&amp;gt;
Frank, K.L., Rogers, D. R., Olins, H. C., Vidoudez, C., &amp;amp;amp; Girguis, P. R. 2013. Characterizing the distribution and rates of microbial sulfate reduction at Middle Valley hydrothermal vents. The ISME journal, 7, 1391–1401. doi:&amp;lt;a href=&amp;quot;http://dx.doi.org/10.1038/ismej.2013.17&amp;quot; target=&amp;quot;_blank&amp;quot;&amp;gt;10.1038/ismej.2013.17&amp;lt;/a&amp;gt;&amp;lt;/p&amp;gt; Methods and Sampling: &amp;lt;p&amp;gt;&amp;lt;strong&amp;gt;Sampling and Analytical Methodology&amp;lt;/strong&amp;gt;: Once on board ship, samples were directly transferred to sterile anaerobic seawater and handled/processed using appropriate sterile microbiological techniques. DNA was extracted from this crushed deposit sample with a protocol modified from (Santelli et al. 2008). Subsamples were washed with 0.1 N HCl, followed by two rinses with a sterile solution containing 10 mM Tris (pH 8.0) and 50 mM EDTA. A known mass of material was added to PowerSoil beadbeating tubes(MoBio Laboratories, Carlsbad CA), incubated at 70 degrees C for 10 minutes, and then amended with 200 ng of poly-A. Subsamples were subjected to beadbeating, followed by three cycles of freeze-thaw steps to further lyse cells. Nucleic acids were extracted using hot phenol (60 degrees C for 3 min.), followed by two chloroform:isoamyl separations and precipitated with ethanol. DNA was resuspended in TE (pH 8.0) and quantified using the Qubit™ fluorometer (Life Technologies, Grand Island, NY).&amp;lt;/p&amp;gt;</gco:CharacterString>
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        <gmx:Anchor xlink:href="http://lod.bco-dmo.org/id/award/554913.rdf" xlink:title="OCE-1061934" xlink:actuate="onRequest">Funding provided by NSF Division of Ocean Sciences (NSF OCE) Award Number: OCE-1061934 Award URL: https://www.nsf.gov/awardsearch/show-award?AWD_ID=1061934</gmx:Anchor>
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