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            <gmx:Anchor xlink:href="http://lod.bco-dmo.org/id/dataset/668475.rdf" xlink:actuate="onRequest">Raw sediment C isotope values collected in Massachusetts from 2012 to 2015</gmx:Anchor>
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            <gco:CharacterString>Cite this dataset as: Spivak, A. (2016) Raw sediment C isotope values collected in Massachusetts from 2012 to 2015. Biological and Chemical Oceanography Data Management Office (BCO-DMO). (Version 1) Version Date 2016-12-02 [if applicable, indicate subset used]. http://lod.bco-dmo.org/id/dataset/668475 [access date]</gco:CharacterString>
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        <gco:CharacterString>Raw sediment C isotope values. Dataset Description: &amp;lt;p&amp;gt;Raw sediment C isotope values.&amp;lt;/p&amp;gt; Methods and Sampling: &amp;lt;p&amp;gt;&amp;lt;strong&amp;gt;Methodology from Spivak, AC and J Ossolinski. 2016. Limited effects of nutrient enrichment on bacterial carbon sources in salt marsh tidal creek sediments. Marine Ecology Progress Series. 544:107-130.&amp;amp;nbsp;&amp;lt;a href=&amp;quot;https://www.researchgate.net/publication/289501077_Limited_effects_of_nutrient_enrichment_on_bacterial_carbon_sources_in_salt_marsh_tidal_creek_sediments&amp;quot; target=&amp;quot;_blank&amp;quot;&amp;gt;10.3354/meps11587&amp;lt;/a&amp;gt;&amp;lt;/strong&amp;gt;&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;Sediment samples for organic matter composition were collected by placing a hard plastic sleeve around a polyvinyl chloride (PVC) corer (5 cm diameter x 15 cm deep) and then removing the corer. The plastic sleeve remained in place to maintain the integrity of the sediment column and mark the core location. The top 0.5 cm of each core was collected into pre-combusted vials and frozen (-80 deg C) until analysis for total organic carbon content and stable isotopes (d&amp;lt;span style=&amp;quot;font-size:10.8333px&amp;quot;&amp;gt;13&amp;lt;/span&amp;gt;C). Samples were dried to constant mass (60 deg C), homogenized with a Retsch Mixer Mill 200, and acidified to remove carbonates prior to analysis by the WHOI Organic Mass Spectrometry Facility with a Carlo Erba 1108 elemental analyzer interfaced to Finnigan-MAT DeltaPlus isotope ratio mass spectrometer (IRMS). Isotopic data are reported as d-values in units of per mil (0/00). For sediments from the isotope labeling experiments, resulting d-values were converted to atom % to calculate excess &amp;lt;span style=&amp;quot;font-size:10.8333px&amp;quot;&amp;gt;13&amp;lt;/span&amp;gt;C (absolute amount &amp;lt;span style=&amp;quot;font-size:10.8333px&amp;quot;&amp;gt;13&amp;lt;/span&amp;gt;C incorporated), using the equations:&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;&amp;lt;img alt=&amp;quot;&amp;quot; src=&amp;quot;https://datadocs.bco-dmo.org/d3/data_docs/Benthic_PP_at_TIDE/equations.png&amp;quot; /&amp;gt;&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;where VPDB is the Vienna Pee Dee Belemnite standard (0.011237) and concentrations are expressed in moles carbon per m2, by accounting for sediment bulk density (0.52 g cm&amp;lt;span style=&amp;quot;font-size:10.8333px&amp;quot;&amp;gt;-3&amp;lt;/span&amp;gt;) and core depth (0.5 cm). Sediment samples collected just prior to application of &amp;lt;span style=&amp;quot;font-size:10.8333px&amp;quot;&amp;gt;13&amp;lt;/span&amp;gt;C-labeled NaHCO&amp;lt;span style=&amp;quot;font-size:10.8333px&amp;quot;&amp;gt;3&amp;lt;/span&amp;gt; or &amp;lt;em&amp;gt;S. alterniflora &amp;lt;/em&amp;gt;detritus served as controls.&amp;lt;/p&amp;gt;</gco:CharacterString>
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        <gmx:Anchor xlink:href="http://lod.bco-dmo.org/id/award/529582.rdf" xlink:title="OCE-1233678" xlink:actuate="onRequest">Funding provided by NSF Division of Ocean Sciences (NSF OCE) Award Number: OCE-1233678 Award URL: https://www.nsf.gov/awardsearch/show-award?AWD_ID=1233678</gmx:Anchor>
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&amp;lt;p&amp;gt;Sediment samples for organic matter composition were collected by placing a hard plastic sleeve around a polyvinyl chloride (PVC) corer (5 cm diameter x 15 cm deep) and then removing the corer. The plastic sleeve remained in place to maintain the integrity of the sediment column and mark the core location. The top 0.5 cm of each core was collected into pre-combusted vials and frozen (-80 deg C) until analysis for total organic carbon content and stable isotopes (d&amp;lt;span style=&amp;quot;font-size:10.8333px&amp;quot;&amp;gt;13&amp;lt;/span&amp;gt;C). Samples were dried to constant mass (60 deg C), homogenized with a Retsch Mixer Mill 200, and acidified to remove carbonates prior to analysis by the WHOI Organic Mass Spectrometry Facility with a Carlo Erba 1108 elemental analyzer interfaced to Finnigan-MAT DeltaPlus isotope ratio mass spectrometer (IRMS). Isotopic data are reported as d-values in units of per mil (0/00). For sediments from the isotope labeling experiments, resulting d-values were converted to atom % to calculate excess &amp;lt;span style=&amp;quot;font-size:10.8333px&amp;quot;&amp;gt;13&amp;lt;/span&amp;gt;C (absolute amount &amp;lt;span style=&amp;quot;font-size:10.8333px&amp;quot;&amp;gt;13&amp;lt;/span&amp;gt;C incorporated), using the equations:&amp;lt;/p&amp;gt;

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&amp;lt;p&amp;gt;where VPDB is the Vienna Pee Dee Belemnite standard (0.011237) and concentrations are expressed in moles carbon per m2, by accounting for sediment bulk density (0.52 g cm&amp;lt;span style=&amp;quot;font-size:10.8333px&amp;quot;&amp;gt;-3&amp;lt;/span&amp;gt;) and core depth (0.5 cm). Sediment samples collected just prior to application of &amp;lt;span style=&amp;quot;font-size:10.8333px&amp;quot;&amp;gt;13&amp;lt;/span&amp;gt;C-labeled NaHCO&amp;lt;span style=&amp;quot;font-size:10.8333px&amp;quot;&amp;gt;3&amp;lt;/span&amp;gt; or &amp;lt;em&amp;gt;S. alterniflora &amp;lt;/em&amp;gt;detritus served as controls.&amp;lt;/p&amp;gt;</gco:CharacterString>
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