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            <gmx:Anchor xlink:href="http://lod.bco-dmo.org/id/dataset/767285.rdf" xlink:actuate="onRequest">Concentrations of dissolved organic carbon and phenols from Polarstern cruise PS 94-ARK-XXIX/3 from August to October 2015</gmx:Anchor>
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            <gco:CharacterString>Cite this dataset as: Kaiser, K. (2019) Concentrations of dissolved organic carbon and phenols from for Polarstern cruise PS 94-ARK-XXIX/3 from August to October 2015. Biological and Chemical Oceanography Data Management Office (BCO-DMO). (Version 1) Version Date 2019-05-10 [if applicable, indicate subset used]. doi:10.1575/1912/bco-dmo.767285.1 [access date]</gco:CharacterString>
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        <gco:CharacterString>Concentrations of dissolved organic carbon and phenols from for Polarstern cruise PS 94-ARK-XXIX/3 Dataset Description:  Methods and Sampling: &amp;lt;p&amp;gt;Samples were filtered straight from Niskin bottles following established protocols for trace-metal clean sampling (Sample handling protocols for GEOTRACES cruises).&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;Samples for DOC concentration were acidified to pH 2.5 and analyzed by high-temperature combustion on a Shimadzu TOC-L. DOC was calculated as the mean of between three and five injections using a six-point standard curve.&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;Lignin-derived phenols were determined following Yan and Kaiser (2018; Anal. Chem), and Yan and Kaiser (2018; Analytica Chimica Acta). Briefly, C18 extracts were redissolved in 200 μL of 1.1 mol L−1 argon- sparged (10 min) NaOH in a 400 uL Teflon vial (Savillex Corp) and amended with containing 500 mg CuO, and amended with 10μL of10 mmolL−1 CuSO4 and 10μ L of 0.2 molL−1 ascorbic acid. Oxidation was at 150 C for 120 minutes. Following oxidation, the samples were spiked with with a surrogate standard mixture of p- hydroxybenzoic acid-13C7, vanillin-13C6, and syringaldehyde-13C6 and acidified to pH ≈ 2.5 with 6 mol L−1 sulfuric acid in the reaction vials.&amp;amp;nbsp; Clean-up of samples was performed with Waters HLB cartrides and final sample eluates were dried under ultra-high purity argon. Phenols were quantified by liquid chromatography/electrospray ionization-tandem mass spectrometry using a five-point calibration curve bracketing the concentration range. Quantified phenols (TDLP included vanillin, acetovanillone, vanillic acid, syringaldehyde, acetosyringone, syringic acid, coumaric acid, ferulic acid, p-hydroxy-benzaldehyde, p-hydroxy-acetophenone, and p-hydroxy-benzoic acid.&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;Samples were filtered straight from Niskin bottles following established protocols for trace-metal clean sampling (Sample handling protocols for GEOTRACES cruises)&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;Samples for DOC concentration were acidified to pH 2.5 and analyzed by high-temperature combustion on a Shimadzu TOC-L. DOC was calculated as the mean of between three and five injections using a six-point standard curve.&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;Lignin-derived phenols were determined following Yan and Kaiser (2018; Anal. Chem), and Yan and Kaiser (2018; Analytica Chimica Acta). Briefly, C18 extracts were redissolved in 200 μL of 1.1 mol L−1 argon- sparged (10 min) NaOH in a 400 uL Teflon vial (Savillex Corp) and amended with containing 500 mg CuO, and amended with 10μL of10 mmolL−1 CuSO4 and 10μ L of 0.2 molL−1 ascorbic acid. Oxidation was at 150 C for 120 minutes. Following oxidation, the samples were spiked with with a surrogate standard mixture of p- hydroxybenzoic acid-13C7, vanillin-13C6, and syringaldehyde-13C6 and acidified to pH ≈ 2.5 with 6 mol L−1 sulfuric acid in the reaction vials.&amp;amp;nbsp; Clean-up of samples was performed with Waters HLB cartrides and final sample eluates were dried under ultra-high purity argon. Phenols were quantified by liquid chromatography/electrospray ionization-tandem mass spectrometry using a five-point calibration curve bracketing the concentration range. Quantified phenols: TDLP included vanillin, acetovanillone, vanillic acid, syringaldehyde, acetosyringone, syringic acid, coumaric acid, ferulic acid, p-hydroxy-benzaldehyde, p-hydroxy-acetophenone, and p-hydroxy-benzoic acid.&amp;lt;/p&amp;gt;</gco:CharacterString>
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        <gmx:Anchor xlink:href="http://lod.bco-dmo.org/id/award/763578.rdf" xlink:title="OCE-1536506" xlink:actuate="onRequest">Funding provided by NSF Division of Ocean Sciences (NSF OCE) Award Number: OCE-1536506 Award URL: https://www.nsf.gov/awardsearch/show-award?AWD_ID=1536506</gmx:Anchor>
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&amp;lt;p&amp;gt;Samples for DOC concentration were acidified to pH 2.5 and analyzed by high-temperature combustion on a Shimadzu TOC-L. DOC was calculated as the mean of between three and five injections using a six-point standard curve.&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;Lignin-derived phenols were determined following Yan and Kaiser (2018; Anal. Chem), and Yan and Kaiser (2018; Analytica Chimica Acta). Briefly, C18 extracts were redissolved in 200 μL of 1.1 mol L−1 argon- sparged (10 min) NaOH in a 400 uL Teflon vial (Savillex Corp) and amended with containing 500 mg CuO, and amended with 10μL of10 mmolL−1 CuSO4 and 10μ L of 0.2 molL−1 ascorbic acid. Oxidation was at 150 C for 120 minutes. Following oxidation, the samples were spiked with with a surrogate standard mixture of p- hydroxybenzoic acid-13C7, vanillin-13C6, and syringaldehyde-13C6 and acidified to pH ≈ 2.5 with 6 mol L−1 sulfuric acid in the reaction vials.&amp;amp;nbsp; Clean-up of samples was performed with Waters HLB cartrides and final sample eluates were dried under ultra-high purity argon. Phenols were quantified by liquid chromatography/electrospray ionization-tandem mass spectrometry using a five-point calibration curve bracketing the concentration range. Quantified phenols (TDLP included vanillin, acetovanillone, vanillic acid, syringaldehyde, acetosyringone, syringic acid, coumaric acid, ferulic acid, p-hydroxy-benzaldehyde, p-hydroxy-acetophenone, and p-hydroxy-benzoic acid.&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;Samples were filtered straight from Niskin bottles following established protocols for trace-metal clean sampling (Sample handling protocols for GEOTRACES cruises)&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;Samples for DOC concentration were acidified to pH 2.5 and analyzed by high-temperature combustion on a Shimadzu TOC-L. DOC was calculated as the mean of between three and five injections using a six-point standard curve.&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;Lignin-derived phenols were determined following Yan and Kaiser (2018; Anal. Chem), and Yan and Kaiser (2018; Analytica Chimica Acta). Briefly, C18 extracts were redissolved in 200 μL of 1.1 mol L−1 argon- sparged (10 min) NaOH in a 400 uL Teflon vial (Savillex Corp) and amended with containing 500 mg CuO, and amended with 10μL of10 mmolL−1 CuSO4 and 10μ L of 0.2 molL−1 ascorbic acid. Oxidation was at 150 C for 120 minutes. Following oxidation, the samples were spiked with with a surrogate standard mixture of p- hydroxybenzoic acid-13C7, vanillin-13C6, and syringaldehyde-13C6 and acidified to pH ≈ 2.5 with 6 mol L−1 sulfuric acid in the reaction vials.&amp;amp;nbsp; Clean-up of samples was performed with Waters HLB cartrides and final sample eluates were dried under ultra-high purity argon. Phenols were quantified by liquid chromatography/electrospray ionization-tandem mass spectrometry using a five-point calibration curve bracketing the concentration range. Quantified phenols: TDLP included vanillin, acetovanillone, vanillic acid, syringaldehyde, acetosyringone, syringic acid, coumaric acid, ferulic acid, p-hydroxy-benzaldehyde, p-hydroxy-acetophenone, and p-hydroxy-benzoic acid.&amp;lt;/p&amp;gt;</gco:CharacterString>
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Developed by Shimadzu, the 680 degree C combustion catalytic oxidation method is now used worldwide. One of its most important features is the capacity to efficiently oxidize hard-to-decompose organic compounds, including insoluble and macromolecular organic compounds. The 680 degree C combustion catalytic oxidation method has been adopted for the TOC-L series.

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