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            <gmx:Anchor xlink:href="http://lod.bco-dmo.org/id/dataset/840875.rdf" xlink:actuate="onRequest">Concentrations of mercury forms and ancillary parameters in size fractionated plankton samples and in water collected during 2014 from Long Island Sound and the adjacent shelf</gmx:Anchor>
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            <gco:CharacterString>Cite this dataset as: Mason, R. P., Gosnell, K. J. (2021) Concentrations of mercury forms and ancillary parameters in size fractionated plankton samples and in water collected during 2014 from Long Island Sound and the adjacent shelf. Biological and Chemical Oceanography Data Management Office (BCO-DMO). (Version 1) Version Date 2021-06-07 [if applicable, indicate subset used]. doi:10.26008/1912/bco-dmo.840875.1 [access date]</gco:CharacterString>
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        <gco:CharacterString>Methods and Sampling: &amp;lt;p&amp;gt;&amp;lt;strong&amp;gt;Sampling and analytical procedures:&amp;lt;/strong&amp;gt;&amp;lt;br /&amp;gt;
Methods are described in detail in Gosnell et al. (2017).&amp;amp;nbsp;&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;Samples were collected to represent three separate seasons during 2014:&amp;amp;nbsp; Spring (May 20th-22nd), Summer (August 2nd-5th), and Fall (September 9th-11th).&amp;amp;nbsp; Plankton and water samples were collected from Western Long Island Sound (WLIS) and Eastern Long Island Sound (ELIS) stations in the spring and summer, while the fall collection included stations in Central Long Island Sound (CLIS), as well as along the shelf break (SB) and mid-shelf (MS) region.&amp;amp;nbsp;&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;At each station, triplicate substations were sampled approximately one mile apart at each site during the spring and summer seasons, while duplicate substations were sampled during the fall. Water samples were collected using a trace-metal clean GoFlo bottle attached to a Kevlar line, or with a trace-metal clean rosette system. Water was kept cold and dark until processing.&amp;amp;nbsp; Water samples were filtered for particulate methylmercury (MeHg) and total mercury (HgT), total suspended solids (TSS) and chlorophyll a (Chl a). Filtrate was saved for dissolved mercury and methylmercury, nutrients, and dissolved organic carbon (DOC) measurements. A CTD was deployed concurrent with water collections, and recorded the vertical profiles of fluorescence, oxygen, temperature, and salinity. Separate phytoplankton (seston) fractions were obtained by sequentially filtering the seawater through polycarbonate filters of sizes 0.2 µm, 5&amp;amp;nbsp;µm&amp;amp;nbsp;and 20 µm. Larger particulate material was excluded by initially passing water through a 200 µm mesh. Zooplankton were collected by attaching an opening/closing 200 µm net (Seatec) to the Kevlar line. Deployments were from 2 meters above the bottom up to 1 meter from the surface. Depths ranged from 11 meter in Long Island Sound, to 100 meter at the Mid-Shelf&amp;amp;nbsp;and Shelf Break stations. Zooplankton were separated into size fractions of 0.2–0.5 millimeters, 0.5–1 mm, 1–2 mm, and&amp;amp;nbsp; &amp;amp;gt;2 mm&amp;amp;nbsp;via mesh screens.&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;Each sample was digested in 4.5 M HNO3 acid solution at 60 degrees C for at least 12 hours prior to analysis. For MeHg analysis, a subsample was neutralized with KOH, diluted to a final volume of 30 mililiters, buffered with acetate buffer (pH of 4.9), and ethylated with sodium tetraethylborate (Hammerschmidt et al. 2013). Water samples were analyzed without acid digestion (Munson et al., 2014). Samples were then analyzed using a Tekran 2700 methylmercury analyzer with cold vapor atomic fluorescence (CVAFS) detection, and an external calibration curve (r2 &amp;amp;gt;0.998). For total Hg analysis (HgT), the remaining digest was diluted, bromine monochloride (BrCl) was added for a minimum 24 hours preceding analysis to decompose organic matter and convert all Hg into the ionic form. Hydroxylamine hydrochloride was added to degrade excess BrCl oxidant prior to analysis using a manual system with tin chloride (SnCl2) reduction, purging with N2 onto a trap containing gold-coated beads for quantification using a Tekran 2500 CVAFS detector, and an external calibration curve (r2 &amp;amp;gt;0.999). For water samples, the acidified water was treated with BrCl and then processed as for biota digests. Chlorophyll and phaeopigment were analyzed using a Trilogy fluorometer, and DOC was analyzed using a Shimazdu TOC/TN instrument.&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;&amp;lt;strong&amp;gt;Additional information:&amp;lt;/strong&amp;gt;&amp;lt;br /&amp;gt;
QA/QC information is given in Table 1. (see Supplemental Files section below)&amp;amp;nbsp;&amp;lt;br /&amp;gt;
&amp;lt;br /&amp;gt;
Results of these data are shown in Figs 2-5 and Table 1 in Gosnell et al. (2017). Additional calculated information (%MeHg, bioconcentration factors) is included in the same paper in additional tables. Stable isotope data for C, N and S for zooplankton is also reported.&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;&amp;lt;strong&amp;gt;Problem report:&amp;lt;/strong&amp;gt;&amp;lt;br /&amp;gt;
Not all size fractions of samples were collected at all locations because of biota variability. Missing information is indicated in the dataset as 'nd'. Additionally,&amp;amp;nbsp;Spring and Summer samples were collected only at two sites with additional Fall&amp;amp;nbsp;sampling at three other sites.&amp;lt;/p&amp;gt;</gco:CharacterString>
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        <gmx:Anchor xlink:href="http://lod.bco-dmo.org/id/award/810508.rdf" xlink:title="OCE-1634048" xlink:actuate="onRequest">Funding provided by NSF Division of Ocean Sciences (NSF OCE) Award Number: OCE-1634048 Award URL: https://www.nsf.gov/awardsearch/show-award?AWD_ID=1634048</gmx:Anchor>
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The accumulation of mercury (Hg) in seafood is a public health concern. The presence of Hg in seafood depends to a large degree on the air-sea exchange of Hg, with atmospheric deposition leading to accumulation of Hg in the ocean. The pathways to seafood start with the uptake of Hg by phytoplankton from seawater where is has always been assumed to accumulate to be eaten by grazers and passed on to larger organisms. This project challenges this assumption with preliminary data that suggests certain phytoplankton species can transform Hg to volatile forms (mercury vapor &amp;amp; dimethylmercury) that are lost to the atmosphere, a processes that removes Hg from the ocean rather than simply concentrating it into the ecosystem and seafood. This process, which has not been studied before, could dramatically alter our view of the Hg cycle in the ocean. The researchers funded by this project will look for the specific phytoplankton species that are capable of volatilizing Hg and quantify the rates at which they do so. They will also examine the suspected role of associated sulfur and selenium compounds in the process, as well as quantifying the changes in the Hg isotopic values for potential use as chemical tracers of the source of Hg in the ecosystem and food supply. These results should allow oceanographers to better quantify and refine our knowledge of Hg cycling in the ocean. The project will support participation of graduate students, a postdoctoral scientist, and incorporation of new information directly into courses taught by the researchers. Funding will also support continuing activities by the participants in activities that disseminate information on mercury and its effect on public and environmental health.&lt;/p&gt;
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	Name: Longitude
	Units: decimal degrees
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	Name: Num_samples
	Units: each
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	Name: MeHg
	Units: picomol per gram (wet weight)
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	Units: picomol per gram (wet weight)
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	Name: HgT
	Units: picomol per gram (wet weight)
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	Name: HgT_stdev
	Units: picomol per gram (wet weight)
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	Name: Depth_description
	Units: units
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	Name: Diss_HgT
	Units: picomol per liter
	Description: &lt;p&gt;Dissolved total mercury (&amp;lt;0.2 µm)&lt;/p&gt; 
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	Name: Diss_MeHg
	Units: picomol per liter
	Description: &lt;p&gt;Dissolved methylmercury (&amp;lt;0.2 µm)&lt;/p&gt; 
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	Name: Part_HgT
	Units: picomol per gram (dry weight)
	Description: &lt;p&gt;Particulate total mercury on a dry weight basis&lt;/p&gt; 
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	Name: Part_MeHg
	Units: picomol per gram (dry weight)
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	Units: milligram per liter (dry weight)
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	Units: microgram per liter (µg/L)
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                <gco:CharacterString>&amp;lt;p&amp;gt;&amp;lt;strong&amp;gt;Sampling and analytical procedures:&amp;lt;/strong&amp;gt;&amp;lt;br /&amp;gt;
Methods are described in detail in Gosnell et al. (2017).&amp;amp;nbsp;&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;Samples were collected to represent three separate seasons during 2014:&amp;amp;nbsp; Spring (May 20th-22nd), Summer (August 2nd-5th), and Fall (September 9th-11th).&amp;amp;nbsp; Plankton and water samples were collected from Western Long Island Sound (WLIS) and Eastern Long Island Sound (ELIS) stations in the spring and summer, while the fall collection included stations in Central Long Island Sound (CLIS), as well as along the shelf break (SB) and mid-shelf (MS) region.&amp;amp;nbsp;&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;At each station, triplicate substations were sampled approximately one mile apart at each site during the spring and summer seasons, while duplicate substations were sampled during the fall. Water samples were collected using a trace-metal clean GoFlo bottle attached to a Kevlar line, or with a trace-metal clean rosette system. Water was kept cold and dark until processing.&amp;amp;nbsp; Water samples were filtered for particulate methylmercury (MeHg) and total mercury (HgT), total suspended solids (TSS) and chlorophyll a (Chl a). Filtrate was saved for dissolved mercury and methylmercury, nutrients, and dissolved organic carbon (DOC) measurements. A CTD was deployed concurrent with water collections, and recorded the vertical profiles of fluorescence, oxygen, temperature, and salinity. Separate phytoplankton (seston) fractions were obtained by sequentially filtering the seawater through polycarbonate filters of sizes 0.2 µm, 5&amp;amp;nbsp;µm&amp;amp;nbsp;and 20 µm. Larger particulate material was excluded by initially passing water through a 200 µm mesh. Zooplankton were collected by attaching an opening/closing 200 µm net (Seatec) to the Kevlar line. Deployments were from 2 meters above the bottom up to 1 meter from the surface. Depths ranged from 11 meter in Long Island Sound, to 100 meter at the Mid-Shelf&amp;amp;nbsp;and Shelf Break stations. Zooplankton were separated into size fractions of 0.2–0.5 millimeters, 0.5–1 mm, 1–2 mm, and&amp;amp;nbsp; &amp;amp;gt;2 mm&amp;amp;nbsp;via mesh screens.&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;Each sample was digested in 4.5 M HNO3 acid solution at 60 degrees C for at least 12 hours prior to analysis. For MeHg analysis, a subsample was neutralized with KOH, diluted to a final volume of 30 mililiters, buffered with acetate buffer (pH of 4.9), and ethylated with sodium tetraethylborate (Hammerschmidt et al. 2013). Water samples were analyzed without acid digestion (Munson et al., 2014). Samples were then analyzed using a Tekran 2700 methylmercury analyzer with cold vapor atomic fluorescence (CVAFS) detection, and an external calibration curve (r2 &amp;amp;gt;0.998). For total Hg analysis (HgT), the remaining digest was diluted, bromine monochloride (BrCl) was added for a minimum 24 hours preceding analysis to decompose organic matter and convert all Hg into the ionic form. Hydroxylamine hydrochloride was added to degrade excess BrCl oxidant prior to analysis using a manual system with tin chloride (SnCl2) reduction, purging with N2 onto a trap containing gold-coated beads for quantification using a Tekran 2500 CVAFS detector, and an external calibration curve (r2 &amp;amp;gt;0.999). For water samples, the acidified water was treated with BrCl and then processed as for biota digests. Chlorophyll and phaeopigment were analyzed using a Trilogy fluorometer, and DOC was analyzed using a Shimazdu TOC/TN instrument.&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;&amp;lt;strong&amp;gt;Additional information:&amp;lt;/strong&amp;gt;&amp;lt;br /&amp;gt;
QA/QC information is given in Table 1. (see Supplemental Files section below)&amp;amp;nbsp;&amp;lt;br /&amp;gt;
&amp;lt;br /&amp;gt;
Results of these data are shown in Figs 2-5 and Table 1 in Gosnell et al. (2017). Additional calculated information (%MeHg, bioconcentration factors) is included in the same paper in additional tables. Stable isotope data for C, N and S for zooplankton is also reported.&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;&amp;lt;strong&amp;gt;Problem report:&amp;lt;/strong&amp;gt;&amp;lt;br /&amp;gt;
Not all size fractions of samples were collected at all locations because of biota variability. Missing information is indicated in the dataset as 'nd'. Additionally,&amp;amp;nbsp;Spring and Summer samples were collected only at two sites with additional Fall&amp;amp;nbsp;sampling at three other sites.&amp;lt;/p&amp;gt;</gco:CharacterString>
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&amp;lt;p&amp;gt;BCO-DMO Processing:&amp;lt;br /&amp;gt;
- data was rearranged to list both Zooplankton and Phytoplankton species by season, location, and size&amp;lt;br /&amp;gt;
- values rounded to four decimal places for MeHg and HgT columns&amp;lt;br /&amp;gt;
- added&amp;amp;nbsp;fields for sample type, size ID, and description of depth&amp;lt;br /&amp;gt;
- replaced asterisk in standard deviation with 'nd' and created a column to list the number of samples&amp;amp;nbsp;&amp;lt;br /&amp;gt;
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          </gmi:identifier>
          <gmi:type>
            <gco:CharacterString>Tekran 2500 Total Mercury Analysis System</gco:CharacterString>
          </gmi:type>
          <gmi:description>
            <gco:CharacterString>PI Supplied Instrument Name: Tekran 2500 Total Mercury Analysis System PI Supplied Instrument Description:Tekran 2500 Total Mercury Analysis System (not automated; cold vapor atomic fluorescence spectrometry) Instrument Name: Tekran 2500 CVAFS mercury detector Instrument Short Name:   Instrument Description: Tekran 2500 Total Mercury Analysis System (not automated; cold vapor atomic fluorescence spectrometry)</gco:CharacterString>
          </gmi:description>
        </gmi:MI_Instrument>
      </gmi:instrument>
      <gmi:instrument>
        <gmi:MI_Instrument>
          <gmi:identifier>
            <gmd:MD_Identifier>
              <gmd:code>
                <gmx:Anchor xlink:href="http://lod.bco-dmo.org/id/instrument/652.rdf" xlink:title="Total Organic Carbon Analyzer" xlink:actuate="onRequest">Shimadzu TOC/TN analyzer</gmx:Anchor>
              </gmd:code>
            </gmd:MD_Identifier>
          </gmi:identifier>
          <gmi:type>
            <gco:CharacterString>Shimadzu TOC/TN analyzer</gco:CharacterString>
          </gmi:type>
          <gmi:description>
            <gco:CharacterString>PI Supplied Instrument Name: Shimadzu TOC/TN analyzer PI Supplied Instrument Description:DOC was analyzed on a Shimadzu TOC/TN analyzer. Instrument Name: Total Organic Carbon Analyzer Instrument Short Name:TOC analyzer   Instrument Description: A unit that accurately determines the carbon concentrations of organic compounds typically by detecting and measuring its combustion product (CO2). See description document at: http://bcodata.whoi.edu/LaurentianGreatLakes_Chemistry/bs116.pdf Community Standard Description: http://vocab.nerc.ac.uk/collection/L05/current/LAB04/</gco:CharacterString>
          </gmi:description>
        </gmi:MI_Instrument>
      </gmi:instrument>
      </gmi:MI_AcquisitionInformation>
  </gmi:acquisitionInformation>
</gmi:MI_Metadata>
