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        <gco:CharacterString>Polysaccharide hydrolysis rates for Marmara Sea, Guaymas Basin, and Eastern Mediterranean Sea sediments Dataset Description: &amp;lt;p&amp;gt;Polysaccharide hydrolysis rates for Marmara Sea, Guaymas Basin, and Eastern Mediterranean Sea sediments. The polysaccharide hydrolysis rates for Marmara Sea sediment were generated during methods development experiments.&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;This dataset contains the final hydrolysis rates. Raw data are also available for download&amp;amp;nbsp;&amp;lt;a href=&amp;quot;http://dmoserv3.whoi.edu/data/C-DEBI/Hoarfrost/GPC-activitydata-SedS.zip&amp;quot; target=&amp;quot;_blank&amp;quot;&amp;gt;in a 20.5 MB .zip file&amp;lt;/a&amp;gt;.&amp;lt;br /&amp;gt;
The .zip file contains&amp;amp;nbsp;GPC chromatographic output for incubations with sediment from Guaymas Basin and the Eastern Mediterranean, used for hydrolysis rate calculations (CoreComparison folder). The &amp;quot;MarmaraMethods&amp;quot; folder contains GPC output for methods development experiments conducted using mud from the Marmara Sea. The &amp;quot;stds&amp;quot; folders contain GPC output for a set of standards of known molecular weight, which are necessary for rate calculations (each folder is a different run – depending on when a sample is run on the GPC, the standards run most recently are used as reference for rate calculations).&amp;amp;nbsp;Each file is raw chromatographic output is in fluorescence units (mV) over time for a 75-minute run.&amp;amp;nbsp;&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;The associated processing an analysis scripts are available through GitHub:&amp;amp;nbsp;&amp;lt;a href=&amp;quot;https://github.com/ahoarfrost/SedS&amp;quot; target=&amp;quot;_blank&amp;quot;&amp;gt;https://github.com/ahoarfrost/SedS&amp;lt;/a&amp;gt;&amp;lt;/p&amp;gt; Methods and Sampling: &amp;lt;p&amp;gt;In the Marmara Sea, surficial sediments were collected by multicorer, and deeper sediments from 570-585 cm and 520-530 cm were collected by gravity corer. Eastern Mediterranean sediments were collected by gravity corer. Guaymas Basin sediments were collected by push core.&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;Sediment incubations with fluorescently labeled organic substrates were set up with three live incubations, a kill control, and one live blank. Incubations were subsampled over time, and each subsample was centrifuged and syringe filtered through a 0.2 um GF filter. Porewater containing partially hydrolyzed fluorescent substrate products were processed using gel permeation chromatography with fluorescence detection. Standards of fluorescent substrates of known molecular weight were also run for the purpose of rate calculations.&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;GPC chromatographic analysis was conducted on a Shimadzu liquid chromatography system and a Hitachi fluorescence detector.&amp;lt;/p&amp;gt;</gco:CharacterString>
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        <gmx:Anchor xlink:href="http://lod.bco-dmo.org/id/award/554980.rdf" xlink:title="OCE-0939564" xlink:actuate="onRequest">Funding provided by NSF Division of Ocean Sciences (NSF OCE) Award Number: OCE-0939564 Award URL: https://www.nsf.gov/awardsearch/show-award?AWD_ID=0939564</gmx:Anchor>
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Heterotrophic organisms are central to subsurface microbial communities and play an important role in carbon cycling. Most approaches to measuring enzymatic activities rely on the addition of a fluorescently labeled substrate to a sediment incubation. However, quantifying rates of extracellular enzymatic hydrolysis of organic matter is often problematic due to the tendency for a fluorescently labeled organic substrate to sorb to the sediment matrix. This results in lower fluorescence intensities and distorted, inaccurate hydrolysis rate calculations. In this project, a desorption treatment was developed to counteract the adverse effects of sorption on enzymatic activity measurements. Upon subsampling a sediment incubation amended with a fluorescently labeled substrate, the subsample is treated with a concentrated solution of unlabeled substrate, along with 0.2% sodium dodecyl sulfate (SDS), in order to competitively desorb the adsorbed, fluorescent substrate target. This treatment improves measured fluorescence intensities by a median of 62.5%, and is particularly effective at desorbing high molecular weight substrate products, resulting in debiased hydrolysis rates that are 14.75 nM/hr lower on average. Competitive desorption treatment was demonstrated to be effective for multiple substrates and in a broad range of sediments from diverse geological and geochemical contexts. Future applications of this method will result in more quantitative and comparable hydrolysis rates in subsurface sediments, will enable enzymatic activity measurements in problematic sediments that were previously infeasible, and will facilitate physiological characterization of microbial communities and model organisms in order to better understand heterotrophic carbon cycling in the subsurface environment.&lt;/p&gt;
&lt;p&gt;This project was funded by a &lt;a href=&quot;http://www.darkenergybiosphere.org/research-activities/research-support/fellowships/&quot; target=&quot;_blank&quot;&gt;C-DEBI Graduate Fellowship&lt;/a&gt;.&lt;/p&gt;</gco:CharacterString>
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http://lod.bco-dmo.org/id/dataset-parameter/671019.rdf
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http://lod.bco-dmo.org/id/dataset-parameter/671021.rdf
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http://lod.bco-dmo.org/id/dataset-parameter/671022.rdf
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http://lod.bco-dmo.org/id/dataset-parameter/671023.rdf
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http://lod.bco-dmo.org/id/dataset-parameter/671024.rdf
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http://lod.bco-dmo.org/id/dataset-parameter/671025.rdf
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