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            <gmx:Anchor xlink:href="http://lod.bco-dmo.org/id/dataset/739646.rdf" xlink:actuate="onRequest">Dissolved and sinking particulate organic nitrogen data from a large volume mesocosm experiment in the Noumea Lagoon, New Caledonia, measured from January to February 2013</gmx:Anchor>
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                        <gco:Date>2019-11-21</gco:Date>
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            <gco:CharacterString>Cite this dataset as: Knapp, A. (2018) Dissolved and sinking particulate organic nitrogen data from a large volume mesocosm experiment in the Noumea Lagoon, New Caledonia, measured from January to February 2013. Biological and Chemical Oceanography Data Management Office (BCO-DMO). (Version 1) Version Date 2018-07-10 [if applicable, indicate subset used]. doi:10.1575/1912/bco-dmo.739646.1 [access date]</gco:CharacterString>
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        <gco:CharacterString>Dataset Description: &amp;lt;p&amp;gt;These data were published in&amp;amp;nbsp;Knapp et al., 2016, Biogeosciences, Supplementary Table 1.&amp;lt;/p&amp;gt; Methods and Sampling: Sampling and analytical procedures: 

The concentration of total nitrogen (TN) for samples was determined by persulfate oxidation (Solorzano and Sharp, 1980) with adaptations (Knapp et al., 2005), and the resulting NO3- was measured by chemiluminescence (Braman and Hendrix, 1989). DON concentration was determined by subtracting the concentrations of PNsusp, NH4+, and NO3-+NO2- (reported in Berthelot et al., 2015, Biogeosciences) from the measured TN concentration of each sample with a propagated error of +/- 0.5 μM.  The d15N of the resulting NO3- was measured using the denitrifier method (Casciotti et al., 2002; McIlvin and Casciotti, 2011; Sigman et al., 2001). 

The d15N of PNsink was measured using a Thermo Scientific Flash 2000 Elemental Analyzer coupled with a Delta Plus Thermo Scientific mass spectrometer. 

The average standard deviation for individual DON concentration measurements was +/- 0.3 µM. DON concentration was determined by subtracting the concentrations of PNsusp, NH4+, and NO3-+NO2- (reported in Berthelot et al., 2015, Biogeosciences) from the measured TN concentration of each sample with a propagated error of +/- 0.5 μM. 

The d15N of TN was determined via persulfate oxidation of TN to NO3-  (Knapp et al., 2005) and subsequent analysis of NO3- d15N by the denitrifier method, with a propagated error for DON d15N calculated using a Monte Carlo method (Press et al., 1992) of +/- 0.6‰. Samples were calibrated with IAEA N3 and USGS 34 NO3- d15N isotopic reference materials as described in McIlvin and Casciotti, 2011. 

The d15N of PNsink was measured using a Thermo Scientific Flash 2000 Elemental Analyzer coupled
with a Delta Plus Thermo Scientific mass spectrometer. The average standard deviation for standards was +/- 0.06‰.</gco:CharacterString>
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        <gmx:Anchor xlink:href="http://lod.bco-dmo.org/id/award/710561.rdf" xlink:title="OCE-1537314" xlink:actuate="onRequest">Funding provided by NSF Division of Ocean Sciences (NSF OCE) Award Number: OCE-1537314 Award URL: https://www.nsf.gov/awardsearch/show-award?AWD_ID=1537314</gmx:Anchor>
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The availability of nitrogen in the surface ocean plays a critical role regulating rates of primary productivity in the ocean, and thus through modification of the carbon cycle, nitrogen has the capacity to influence climate. The dominant source of biologically available nitrogen to the ocean is through a process known as di-nitrogen (N2) fixation, which involves the reduction of N2 gas dissolved in seawater to ammonium by microbes referred to as diazotrophs. While significant progress has been made identifying a diversity of marine diazotrophs in recent years using molecular tools, quantifying global rates of N2 fixation, and identifying which ocean basin supports the highest fluxes, has remained a vexing question. This research will quantify rates of N2 fixation as well as its importance for supporting production in the southwest Pacific Ocean. Results from this research will shed light on the sensitivities of N2 fixation (temperature, iron concentrations) as well as the extent of spatial and temporal coupling of nitrogen sources and sinks in the ocean. The work will be carried out by an early career scientist, and involve mentoring of young women, middle school girls and minorities, training of undergraduate and graduate researchers, and international collaborations.&lt;/p&gt;
&lt;p&gt;Identifying the spatial distribution of the largest di-nitrogen (N2) fixation fluxes to the ocean remains a critical goal of chemical oceanography. The spatial distribution can inform our understanding of the environmental sensitivities of N2 fixation and the capacity for the dominant marine nitrogen (N) source and sink processes to respond to each other and thus influence the global carbon cycle and climate. In addition to temperature, two factors are at the heart of the current debate over what influences the spatial distribution of N2 fixation in the ocean: 1) the presence of adequate iron to meet the needs of N2 fixing microbes, and, 2) the absolute concentrations as well as ratios of surface ocean nitrate and phosphate concentrations that are low relative to the &quot;Redfield&quot; ratio, which are thought to favor N2 fixing microbes. This project will test the effects of gradients in atmospheric dust deposition on N2 fixation rates when surface waters have relatively constant but favorable nitrate to phosphate concentrations. The work will be carried out in the southwest Pacific, a region highlighted by new modeling work for its unique geochemical characteristics that are expected to favor significant N2 fixation fluxes. Nitrate+nitrite d15N as well as total dissolved nitrogen (TDN) concentration and d15N will be measured in water column samples collected on a French cruise and sediment traps were deployed to capture the sinking particulate N flux. The results will be compared with published work to evaluate which ocean regions support the largest N2 fixation fluxes.&lt;/p&gt;
&lt;p&gt;More information:&lt;/p&gt;
&lt;p&gt;This project was part of the Oligotrophy to UlTra-oligotrophy PACific Experiment (OUTPACE) cruise in the Southwest Pacific between New Caledonia (166°28' E; 22°14' S) and Tahiti (149°36' W; 17°34' S) 0-2000 m&lt;br /&gt;
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The concentration of total nitrogen (TN) for samples was determined by persulfate oxidation (Solorzano and Sharp, 1980) with adaptations (Knapp et al., 2005), and the resulting NO3- was measured by chemiluminescence (Braman and Hendrix, 1989). DON concentration was determined by subtracting the concentrations of PNsusp, NH4+, and NO3-+NO2- (reported in Berthelot et al., 2015, Biogeosciences) from the measured TN concentration of each sample with a propagated error of +/- 0.5 μM.  The d15N of the resulting NO3- was measured using the denitrifier method (Casciotti et al., 2002; McIlvin and Casciotti, 2011; Sigman et al., 2001). 

The d15N of PNsink was measured using a Thermo Scientific Flash 2000 Elemental Analyzer coupled with a Delta Plus Thermo Scientific mass spectrometer. 

The average standard deviation for individual DON concentration measurements was +/- 0.3 µM. DON concentration was determined by subtracting the concentrations of PNsusp, NH4+, and NO3-+NO2- (reported in Berthelot et al., 2015, Biogeosciences) from the measured TN concentration of each sample with a propagated error of +/- 0.5 μM. 

The d15N of TN was determined via persulfate oxidation of TN to NO3-  (Knapp et al., 2005) and subsequent analysis of NO3- d15N by the denitrifier method, with a propagated error for DON d15N calculated using a Monte Carlo method (Press et al., 1992) of +/- 0.6‰. Samples were calibrated with IAEA N3 and USGS 34 NO3- d15N isotopic reference materials as described in McIlvin and Casciotti, 2011. 

The d15N of PNsink was measured using a Thermo Scientific Flash 2000 Elemental Analyzer coupled
with a Delta Plus Thermo Scientific mass spectrometer. The average standard deviation for standards was +/- 0.06‰.</gco:CharacterString>
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  Instrument Name: Elemental Analyzer Instrument Short Name:   Instrument Description: Instruments that quantify carbon, nitrogen and sometimes other elements by combusting the sample at very high temperature and assaying the resulting gaseous oxides. Usually used for samples including organic material. Community Standard Description: http://vocab.nerc.ac.uk/collection/L05/current/LAB01/</gco:CharacterString>
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