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            <gmx:Anchor xlink:href="http://lod.bco-dmo.org/id/dataset/817797.rdf" xlink:actuate="onRequest">Sediment geochemistry from push cores collected during HOV Alvin dives during the R/V Atlantis cruise AT42-05 in Guaymas Basin, Gulf of California (27 00.00 N, -111 20.00 W) in November 2018</gmx:Anchor>
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                <gmx:Anchor xlink:href="http://orcid.org/0000-0003-1610-451X" xlink:title="ORCID" xlink:actuate="onRequest">Samantha B. Joye</gmx:Anchor>
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                <gmx:Anchor xlink:href="https://ror.org/0130frc33" xlink:title="ROR ID" xlink:actuate="onRequest">University of North Carolina at Chapel Hill</gmx:Anchor>
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            <gco:CharacterString>Cite this dataset as: Joye, S. B., Teske, A. P., Peterson, R. N. (2021) Sediment geochemistry from push cores collected during HOV Alvin dives during the R/V Atlantis cruise AT42-05 in Guaymas Basin, Gulf of California (27 00.00 N, -111 20.00 W) in November 2018. Biological and Chemical Oceanography Data Management Office (BCO-DMO). (Version 1) Version Date 2020-07-02 [if applicable, indicate subset used]. doi:10.26008/1912/bco-dmo.817797.1 [access date]</gco:CharacterString>
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        <gco:CharacterString>Sediment geochemistry AT42-05 Dataset Description: &amp;lt;p&amp;gt;Sediment geochemistry from push cores obtained using the human-occupied deep-diving vehicle (HOV) Alvin dives 4991-5000 during the R/V Atlantis cruise AT42-05 in Guaymas Basin, Gulf of California (27 00.00 N, -111 20.00 W) in November&amp;amp;nbsp; 2018.&amp;lt;/p&amp;gt; Methods and Sampling: &amp;lt;p&amp;gt;Sediment samples were collected by the DSV Alvin using PVC push cores.&amp;amp;nbsp; Upon arrival at the surface the cores were described and cataloged prior to being sectioned into discrete depth intervals.&amp;amp;nbsp; Porewater was separated from the sediment using a manually-actuated pore water press.&amp;amp;nbsp; Porewater and sediment samples were preserved and analyzed as follows:&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;1) Nutrients (DOC, TDN, NOx, NO2, NH4, PO4, TDP): Porewater sample was filtered through a pre-rinsed 0.2 um regenerated cellulose Target2 syringe filter (Thermo Scientific, Prod. No. F25047), collected into an HDPE bottle and stored frozen at -20°C until analysis.&amp;amp;nbsp; Individual analytes were analyzed as follows:&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;DOC was determined using high temperature catalytic combustion and an NDIR detector following the method described in Sugimura and Suzuki, 1988 (&amp;lt;em&amp;gt;A high-temperature catalytic oxidation method for the determination of non-volatile dissolved organic carbon in seawater by direct injection of liquid sample. Mar. Chem., 24: 105-131&amp;lt;/em&amp;gt;).&amp;amp;nbsp;&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;TDN was determined using high temperature combustion and a chemiluminescence detector following the method described in Watanabe et. al, 2007 (&amp;lt;em&amp;gt;Conversion efficiency of the high-temperature combustion technique for dissolved organic carbon and total dissolved nitrogen analysis.&amp;amp;nbsp; Intern. J. Environ. Anal. Chem., 87: 387-399&amp;lt;/em&amp;gt;).&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;NOx was determined using chemical reduction and a nitric oxide detector following the method described by Garside, 1982 (&amp;lt;em&amp;gt;A chemiluminescent technique for the determination of nanomolar concentrations of nitrate and nitrite in seawater. Mar. Chem. 11: 159-167&amp;lt;/em&amp;gt;).&amp;amp;nbsp;&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;NO2 was determined using the colorimetric method described by Bendschneider and Robinson, 1952 (&amp;lt;em&amp;gt;A new spectrophotometric method for the determination of nitrite in sea water.&amp;lt;/em&amp;gt; J. &amp;lt;em&amp;gt;Mar. Res.&amp;lt;/em&amp;gt;, 11: 87) as reproduced by Parsons, Marta, and Lalli, 1984 (&amp;lt;em&amp;gt;Determination of Nitrite. &amp;lt;/em&amp;gt;&amp;amp;nbsp;&amp;lt;em&amp;gt;A manual of chemical and biological methods for seawater analysis pp. 7-9&amp;lt;/em&amp;gt;).&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;NH4 was determined using the colorimetric method described by Solorzano, 1969 (&amp;lt;em&amp;gt;Determination of ammonia in natural waters by the phenolhypochlorite method.&amp;lt;/em&amp;gt;&amp;amp;nbsp; &amp;lt;em&amp;gt;Limnol. Oceanogr., 14: 799-801&amp;lt;/em&amp;gt;).&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;PO4 was determined using the colorimetric method described by Strickland and Parsons, 1972 (&amp;lt;em&amp;gt;Determination of reactive phosphorus&amp;lt;/em&amp;gt;. &amp;lt;em&amp;gt;A practical handbook of seawater analysis. Fisheries Research Board of Canada, pp. 49-52&amp;lt;/em&amp;gt;).&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;TDP was determined using the colorimetric method described by Solorzano and Sharp, 1980 (&amp;lt;em&amp;gt;Determination of total dissolved phosphorous and particulate phosphorous in natural waters.&amp;lt;/em&amp;gt;&amp;amp;nbsp; &amp;lt;em&amp;gt;Limnol. Oceanogr., 25: 754-758).&amp;lt;/em&amp;gt;&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;Sediment pH was determined using a sediment probe (Oakton, Prod. No. 35634-50) and measured immediately during core sectioning; the probe was calibrated using NBS standards.&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;Pore water pH was determined using a Ross electrode (Thermo Fisher, Prod. No. 8103BNUWP) that was calibrated using NBS standards.&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;2) Alkalinity: Porewater alkalinity was determined using the spectrophotometric method described by Sarazin et al., 1999 (&amp;lt;em&amp;gt;A rapid and accurate spectroscopic method for alkalinity measurements in sea water samples. Water Research 33:290-294)./&amp;lt;/em&amp;gt;&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;3) CH4: Sediment samples (3 cubic centimeters) were collected into a glass serum vial, preserved with 1M NaOH (3 milliliters), crimp-sealed with a butyl rubber stopper and stored at room temperature until analysis.&amp;amp;nbsp; CH4 was determined by headspace analysis using an SRI 8610C gas chromatograph equipped with a flame ionization detector and SRI Hayesep D 6’x1/8” column (Prod. No. 8600-PKDB).&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;4) H2S: Porewater sample was collected into a 15 mL centrifuge tube containing 2M zinc acetate and stored at 5°C until analysis.&amp;amp;nbsp; H2S was determined using the colorimetric method described by Cline, 1969 (&amp;lt;em&amp;gt;Spectrophotometric determination of hydrogen sulfide in natural waters.&amp;amp;nbsp; Limnol. Oceanogr., 14: 454-458&amp;lt;/em&amp;gt;).&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;5) Sulfate (SO4): Porewater sample was filtered through a pre-rinsed 0.2 μm regenerated cellulose Target2 syringe filter (Thermo Scientific, Prod. No. F25047) into a 7 mL scintillation vial. Samples were acidified with 10 μL of concentrated HNO3 per 1 mL sample, sealed with a PTFE lined cap, and stored at room temperature until analysis. Sample analysis was performed using KOH eluent supplied by a Dionex EGC III KOH Eluent Generator Cartridge (Prod. No. 074532), Dionex CR-ATC Continuously Regenerated Trap Column (Prod. No. 060477), Dionex AERS 500 Electronically Regenerated Suppressor (Prod. No. 082541), Dionex IonPac AG19 Guard Column (Prod. No. 062888), Dionex IonPac AS19 Analytical Column (Prod. No. 062886) and Dionex CRD 200 RFIC Carbonate Removal Device (Prod. No. 062986). Reference - Weston et al. 2006, Biogeochemistry 77: 375-408.&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;6) Chloride (Cl): Porewater sample was filtered through a pre-rinsed 0.2 μm regenerated cellulose Target2 syringe filter (Thermo Scientific, Prod. No. F25047) into a 7 mL scintillation vial. Samples were acidified with 10 μL of concentrated HNO3 per 1 mL sample, sealed with a PTFE lined cap, and stored at room temperature until analysis. Sample analysis was performed using KOH eluent supplied by a Dionex EGC III KOH Eluent Generator Cartridge (Prod. No. 074532), Dionex CR-ATC Continuously Regenerated Trap Column (Prod. No. 060477), Dionex AERS 500 Electronically Regenerated Suppressor (Prod. No. 082541), Dionex IonPac AG19 Guard Column (Prod. No. 062888), Dionex IonPac AS19 Analytical Column (Prod. No. 062886) and Dionex CRD 200 RFIC Carbonate Removal Device (Prod. No. 062986). Reference - Weston et al. 2006, Biogeochemistry 77: 375-408.&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;7) Calculated Values: Values for NO3, DIN, DON, DOP were calculated as follows:&amp;lt;br /&amp;gt;
NO3 = NOx - NO2&amp;lt;br /&amp;gt;
DIN = NOx + NH4&amp;lt;br /&amp;gt;
DON = TDN - DIN&amp;lt;br /&amp;gt;
DOP= TDP - PO4&amp;lt;/p&amp;gt;</gco:CharacterString>
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        <gmx:Anchor xlink:href="http://lod.bco-dmo.org/id/award/505556.rdf" xlink:title="OCE-1357360" xlink:actuate="onRequest">Funding provided by NSF Division of Ocean Sciences (NSF OCE) Award Number: OCE-1357360 Award URL: https://www.nsf.gov/awardsearch/show-award?AWD_ID=1357360</gmx:Anchor>
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            <gmx:Anchor xlink:href="http://orcid.org/0000-0003-1610-451X" xlink:title="ORCID" xlink:actuate="onRequest">Samantha B. Joye</gmx:Anchor>
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Hydrothermally active sediments in the Guaymas Basin are dominated by novel microbial communities that catalyze important biogeochemical processes in these seafloor ecosystems. This project will investigate genomic potential, physiological capabilities and biogeochemical roles of key uncultured organisms from Guaymas sediments, especially the high-temperature anaerobic methane oxidizers that occur specifically in hydrothermally active sediments (ANME-1Guaymas). The study will focus on their role in carbon transformations, but also explore their potential involvement in sulfur and nitrogen transformations. First-order research topics include quantifying anaerobic methane oxidation under high temperature,in situ concentrations of phosphorus and methane , and with alternate electron acceptors; sulfate and sulfur-dependent microbial pathways and isotopic signatures under these conditions; and nitrogen transformations in methane-oxidizing microbial communities, hydrothermal mats and sediments.&lt;/p&gt;
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	Name: ALVIN_Dive
	Units: unitless
	Description: &lt;p&gt;Alvin dive number&lt;/p&gt; 
http://lod.bco-dmo.org/id/dataset-parameter/818115.rdf
	Name: Site
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http://lod.bco-dmo.org/id/dataset-parameter/818116.rdf
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http://lod.bco-dmo.org/id/dataset-parameter/818117.rdf
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http://lod.bco-dmo.org/id/dataset-parameter/818118.rdf
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http://lod.bco-dmo.org/id/dataset-parameter/818119.rdf
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http://lod.bco-dmo.org/id/dataset-parameter/818120.rdf
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http://lod.bco-dmo.org/id/dataset-parameter/818121.rdf
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http://lod.bco-dmo.org/id/dataset-parameter/818122.rdf
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http://lod.bco-dmo.org/id/dataset-parameter/818123.rdf
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http://lod.bco-dmo.org/id/dataset-parameter/818124.rdf
	Name: salinity
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http://lod.bco-dmo.org/id/dataset-parameter/818125.rdf
	Name: NO2_uM
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http://lod.bco-dmo.org/id/dataset-parameter/818126.rdf
	Name: NO2_uM_bdl
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http://lod.bco-dmo.org/id/dataset-parameter/818127.rdf
	Name: Nox_uM
	Units: micromol/L
	Description: &lt;p&gt;Pore water concentrations of nitrite and nitrate; method detection limit = 0.2&lt;/p&gt; 
http://lod.bco-dmo.org/id/dataset-parameter/818128.rdf
	Name: NO3_uM
	Units: micromol/L
	Description: &lt;p&gt;Pore water concentrations of nitrate (Nox - NO2); method detection limit = 0.1&lt;/p&gt; 
http://lod.bco-dmo.org/id/dataset-parameter/818129.rdf
	Name: DIN_uM
	Units: micromol/L
	Description: &lt;p&gt;Pore water concentrations of dissolved inorganic nitrogen; method detection limit = 0.2&lt;/p&gt; 
http://lod.bco-dmo.org/id/dataset-parameter/818130.rdf
	Name: TDN_uM
	Units: micromol/L
	Description: &lt;p&gt;Pore water concentrations of total dissolved nitrogen; method detection limit = 0.5&lt;/p&gt; 
http://lod.bco-dmo.org/id/dataset-parameter/818131.rdf
	Name: NH4_uM
	Units: micromol/L
	Description: &lt;p&gt;Pore water concentrations of ammonium; method detection limit = 0.1&lt;/p&gt; 
http://lod.bco-dmo.org/id/dataset-parameter/818132.rdf
	Name: DON_uM
	Units: micromol/L
	Description: &lt;p&gt;Pore water concentrations of dissolved organic nitrogen; method detection limit = 1&lt;/p&gt; 
http://lod.bco-dmo.org/id/dataset-parameter/818133.rdf
	Name: PO4_uM
	Units: micromol/L
	Description: &lt;p&gt;Pore water concentrations of phosphate; method detection limit = 0.1&lt;/p&gt; 
http://lod.bco-dmo.org/id/dataset-parameter/818134.rdf
	Name: TDP_uM
	Units: micromol/L
	Description: &lt;p&gt;Pore water concentrations of total dissolved phosphate; method detection limit = 0.1&lt;/p&gt; 
http://lod.bco-dmo.org/id/dataset-parameter/818135.rdf
	Name: DOP_uM
	Units: micromol/L
	Description: &lt;p&gt;Pore water concentrations of dissolved organic phosphate; method detection limit = 0.1&lt;/p&gt; 
http://lod.bco-dmo.org/id/dataset-parameter/818136.rdf
	Name: DOP_uM_bdl
	Units: unitless
	Description: &lt;p&gt;BDL flag for pore water concentrations of dissolved organic phosphate (bdl = below detection limit); method detection limit = 0.1&lt;/p&gt; 
http://lod.bco-dmo.org/id/dataset-parameter/818137.rdf
	Name: DIN_DIP
	Units: unitless
	Description: &lt;p&gt;Pore water ratios of dissolved inorganic nitrogen to dissolved inorganic phosphate; method detection limit = 0.1&lt;/p&gt; 
http://lod.bco-dmo.org/id/dataset-parameter/818138.rdf
	Name: DON_DOP
	Units: unitless
	Description: &lt;p&gt;Pore water ratios of dissolved organic nitrogen to dissolved organic phosphate; method detection limit = 0.5&lt;/p&gt; 
http://lod.bco-dmo.org/id/dataset-parameter/818139.rdf
	Name: DOC_uM
	Units: micromol/L
	Description: &lt;p&gt;Porewater concentrations of dissolved organic carbon; method detection limit = 1&lt;/p&gt; 
http://lod.bco-dmo.org/id/dataset-parameter/818140.rdf
	Name: Alkalinity_mM
	Units: mmol/L
	Description: &lt;p&gt;Pore water alkalinity; method detection limit = 0.05&lt;/p&gt; 
http://lod.bco-dmo.org/id/dataset-parameter/818141.rdf
	Name: CH4_uM
	Units: micromol/L
	Description: &lt;p&gt;Pore water concentrations of methane; method detection limit = 0.1&lt;/p&gt; 
http://lod.bco-dmo.org/id/dataset-parameter/818142.rdf
	Name: H2S_mM
	Units: mmol/L
	Description: &lt;p&gt;Pore water concentrations of hydrogen sulfide; method detection limit = 0.1&lt;/p&gt; 
http://lod.bco-dmo.org/id/dataset-parameter/818143.rdf
	Name: H2S_mM_bdl
	Units: unitless
	Description: &lt;p&gt;BDL flag for pore water concentrations of hydrogen sulfide (bdl = below detection limit); method detection limit = 0.1&lt;/p&gt; 
http://lod.bco-dmo.org/id/dataset-parameter/818144.rdf
	Name: Sulfate_mM
	Units: mmol/L
	Description: &lt;p&gt;Pore water concentrations of sulfate; method detection limit = 0.1&lt;/p&gt; 
http://lod.bco-dmo.org/id/dataset-parameter/818145.rdf
	Name: Chloride_mM
	Units: mmol/L
	Description: &lt;p&gt;Pore water concentrations of chloride&lt;/p&gt; 
http://lod.bco-dmo.org/id/dataset-parameter/818146.rdf
	Name: Porosity_pcent
	Units: %
	Description: &lt;p&gt;Sediment porosity&lt;/p&gt; 
http://lod.bco-dmo.org/id/dataset-parameter/818147.rdf
	Name: SOM_LOI_pcent
	Units: %
	Description: &lt;p&gt;Sediment organic matter (Loss on ignition); method detection limit = 0.2&lt;/p&gt; 
http://lod.bco-dmo.org/id/dataset-parameter/818148.rdf
	Name: TPN_pcent
	Units: %
	Description: &lt;p&gt;Sediment total particulate nitrogen&lt;/p&gt; 
http://lod.bco-dmo.org/id/dataset-parameter/818149.rdf
	Name: TPC_pcent
	Units: %
	Description: &lt;p&gt;Sediment total particulate carbon&lt;/p&gt; 
http://lod.bco-dmo.org/id/dataset-parameter/818150.rdf
	Name: POC_pcent
	Units: %
	Description: &lt;p&gt;Sediment particulate organic carbon&lt;/p&gt; 
http://lod.bco-dmo.org/id/dataset-parameter/818151.rdf
	Name: PIC_pcent
	Units: %
	Description: &lt;p&gt;Sediment particulate inorganic carbon&lt;/p&gt; 
http://lod.bco-dmo.org/id/dataset-parameter/818152.rdf
	Name: PIC_pcent_bdl
	Units: unitless
	Description: &lt;p&gt;BDL flag for sediment particulate inorganic carbon (bdl = below detection limit)&lt;/p&gt; 
http://lod.bco-dmo.org/id/dataset-parameter/818153.rdf
	Name: TPP_umol_P_g_sediment
	Units: micromol P/gram sediment
	Description: &lt;p&gt;Sediment total particulate phosphate&lt;/p&gt; 
http://lod.bco-dmo.org/id/dataset-parameter/818154.rdf
	Name: TPP_pcent
	Units: %
	Description: &lt;p&gt;Sediment total particulate phosphate (percent)&lt;/p&gt; 
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                <gco:CharacterString>&amp;lt;p&amp;gt;Sediment samples were collected by the DSV Alvin using PVC push cores.&amp;amp;nbsp; Upon arrival at the surface the cores were described and cataloged prior to being sectioned into discrete depth intervals.&amp;amp;nbsp; Porewater was separated from the sediment using a manually-actuated pore water press.&amp;amp;nbsp; Porewater and sediment samples were preserved and analyzed as follows:&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;1) Nutrients (DOC, TDN, NOx, NO2, NH4, PO4, TDP): Porewater sample was filtered through a pre-rinsed 0.2 um regenerated cellulose Target2 syringe filter (Thermo Scientific, Prod. No. F25047), collected into an HDPE bottle and stored frozen at -20°C until analysis.&amp;amp;nbsp; Individual analytes were analyzed as follows:&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;DOC was determined using high temperature catalytic combustion and an NDIR detector following the method described in Sugimura and Suzuki, 1988 (&amp;lt;em&amp;gt;A high-temperature catalytic oxidation method for the determination of non-volatile dissolved organic carbon in seawater by direct injection of liquid sample. Mar. Chem., 24: 105-131&amp;lt;/em&amp;gt;).&amp;amp;nbsp;&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;TDN was determined using high temperature combustion and a chemiluminescence detector following the method described in Watanabe et. al, 2007 (&amp;lt;em&amp;gt;Conversion efficiency of the high-temperature combustion technique for dissolved organic carbon and total dissolved nitrogen analysis.&amp;amp;nbsp; Intern. J. Environ. Anal. Chem., 87: 387-399&amp;lt;/em&amp;gt;).&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;NOx was determined using chemical reduction and a nitric oxide detector following the method described by Garside, 1982 (&amp;lt;em&amp;gt;A chemiluminescent technique for the determination of nanomolar concentrations of nitrate and nitrite in seawater. Mar. Chem. 11: 159-167&amp;lt;/em&amp;gt;).&amp;amp;nbsp;&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;NO2 was determined using the colorimetric method described by Bendschneider and Robinson, 1952 (&amp;lt;em&amp;gt;A new spectrophotometric method for the determination of nitrite in sea water.&amp;lt;/em&amp;gt; J. &amp;lt;em&amp;gt;Mar. Res.&amp;lt;/em&amp;gt;, 11: 87) as reproduced by Parsons, Marta, and Lalli, 1984 (&amp;lt;em&amp;gt;Determination of Nitrite. &amp;lt;/em&amp;gt;&amp;amp;nbsp;&amp;lt;em&amp;gt;A manual of chemical and biological methods for seawater analysis pp. 7-9&amp;lt;/em&amp;gt;).&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;NH4 was determined using the colorimetric method described by Solorzano, 1969 (&amp;lt;em&amp;gt;Determination of ammonia in natural waters by the phenolhypochlorite method.&amp;lt;/em&amp;gt;&amp;amp;nbsp; &amp;lt;em&amp;gt;Limnol. Oceanogr., 14: 799-801&amp;lt;/em&amp;gt;).&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;PO4 was determined using the colorimetric method described by Strickland and Parsons, 1972 (&amp;lt;em&amp;gt;Determination of reactive phosphorus&amp;lt;/em&amp;gt;. &amp;lt;em&amp;gt;A practical handbook of seawater analysis. Fisheries Research Board of Canada, pp. 49-52&amp;lt;/em&amp;gt;).&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;TDP was determined using the colorimetric method described by Solorzano and Sharp, 1980 (&amp;lt;em&amp;gt;Determination of total dissolved phosphorous and particulate phosphorous in natural waters.&amp;lt;/em&amp;gt;&amp;amp;nbsp; &amp;lt;em&amp;gt;Limnol. Oceanogr., 25: 754-758).&amp;lt;/em&amp;gt;&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;Sediment pH was determined using a sediment probe (Oakton, Prod. No. 35634-50) and measured immediately during core sectioning; the probe was calibrated using NBS standards.&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;Pore water pH was determined using a Ross electrode (Thermo Fisher, Prod. No. 8103BNUWP) that was calibrated using NBS standards.&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;2) Alkalinity: Porewater alkalinity was determined using the spectrophotometric method described by Sarazin et al., 1999 (&amp;lt;em&amp;gt;A rapid and accurate spectroscopic method for alkalinity measurements in sea water samples. Water Research 33:290-294)./&amp;lt;/em&amp;gt;&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;3) CH4: Sediment samples (3 cubic centimeters) were collected into a glass serum vial, preserved with 1M NaOH (3 milliliters), crimp-sealed with a butyl rubber stopper and stored at room temperature until analysis.&amp;amp;nbsp; CH4 was determined by headspace analysis using an SRI 8610C gas chromatograph equipped with a flame ionization detector and SRI Hayesep D 6’x1/8” column (Prod. No. 8600-PKDB).&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;4) H2S: Porewater sample was collected into a 15 mL centrifuge tube containing 2M zinc acetate and stored at 5°C until analysis.&amp;amp;nbsp; H2S was determined using the colorimetric method described by Cline, 1969 (&amp;lt;em&amp;gt;Spectrophotometric determination of hydrogen sulfide in natural waters.&amp;amp;nbsp; Limnol. Oceanogr., 14: 454-458&amp;lt;/em&amp;gt;).&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;5) Sulfate (SO4): Porewater sample was filtered through a pre-rinsed 0.2 μm regenerated cellulose Target2 syringe filter (Thermo Scientific, Prod. No. F25047) into a 7 mL scintillation vial. Samples were acidified with 10 μL of concentrated HNO3 per 1 mL sample, sealed with a PTFE lined cap, and stored at room temperature until analysis. Sample analysis was performed using KOH eluent supplied by a Dionex EGC III KOH Eluent Generator Cartridge (Prod. No. 074532), Dionex CR-ATC Continuously Regenerated Trap Column (Prod. No. 060477), Dionex AERS 500 Electronically Regenerated Suppressor (Prod. No. 082541), Dionex IonPac AG19 Guard Column (Prod. No. 062888), Dionex IonPac AS19 Analytical Column (Prod. No. 062886) and Dionex CRD 200 RFIC Carbonate Removal Device (Prod. No. 062986). Reference - Weston et al. 2006, Biogeochemistry 77: 375-408.&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;6) Chloride (Cl): Porewater sample was filtered through a pre-rinsed 0.2 μm regenerated cellulose Target2 syringe filter (Thermo Scientific, Prod. No. F25047) into a 7 mL scintillation vial. Samples were acidified with 10 μL of concentrated HNO3 per 1 mL sample, sealed with a PTFE lined cap, and stored at room temperature until analysis. Sample analysis was performed using KOH eluent supplied by a Dionex EGC III KOH Eluent Generator Cartridge (Prod. No. 074532), Dionex CR-ATC Continuously Regenerated Trap Column (Prod. No. 060477), Dionex AERS 500 Electronically Regenerated Suppressor (Prod. No. 082541), Dionex IonPac AG19 Guard Column (Prod. No. 062888), Dionex IonPac AS19 Analytical Column (Prod. No. 062886) and Dionex CRD 200 RFIC Carbonate Removal Device (Prod. No. 062986). Reference - Weston et al. 2006, Biogeochemistry 77: 375-408.&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;7) Calculated Values: Values for NO3, DIN, DON, DOP were calculated as follows:&amp;lt;br /&amp;gt;
NO3 = NOx - NO2&amp;lt;br /&amp;gt;
DIN = NOx + NH4&amp;lt;br /&amp;gt;
DON = TDN - DIN&amp;lt;br /&amp;gt;
DOP= TDP - PO4&amp;lt;/p&amp;gt;</gco:CharacterString>
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- data submitted in Excel file &amp;quot;Joye_OCE_1357360_Data_Submission_AT4205_sediment.xlsx&amp;quot; sheet 1 extracted to csv&amp;lt;br /&amp;gt;
- added conventional header with dataset name, PI name, version date&amp;lt;br /&amp;gt;
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