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            <gco:CharacterString>Cite this dataset as: Hu, H., Yeung, L., Berelson, W., Young, E. (2018) Depth profiles of dissolved O2 saturation and isotopologues from the R/V Yellowfin and R/V Kilo Moana from 2016-09-14 to 2017-08-28. Biological and Chemical Oceanography Data Management Office (BCO-DMO). (Version 1) Version Date 2018-11-30 [if applicable, indicate subset used]. doi:10.1575/1912/bco-dmo.753594.1 [access date]</gco:CharacterString>
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        <gco:CharacterString>Depth profiles of dissolved O2 saturation and isotopologues Dataset Description: &amp;lt;p&amp;gt;Seawater was sampled from Niskin bottles associated with CTD casts on each cruise. Water for these dissolved gas isotope samples was the first to be sampled from a given Niskin bottle. When possible, bottles from the same cast were sampled, but depth profiles often came from separate casts at the same site.&amp;amp;nbsp;&amp;lt;/p&amp;gt; Methods and Sampling: &amp;lt;p&amp;gt;In general, procedures followed those of Reuer et al. 2007. Briefly, 1 and 2-L bottles were pre-poisoned with 200 μL and 400 μL saturated HgCl2 solution, dried, and then evacuated to a pressure of &amp;amp;lt; 10-3 mbar before the gas-tight valve was closed. The Louwer-Hapert 9mm valve sidearm was then filled with distilled water and capped, making sure to remove all visible bubbles, to retard any atmospheric leaks. During sampling, water from the bottom of the Niskin flask was allowed to flow into the sidearm for several seconds (to flush out the distilled water) before the vacuum valve was opened to allow water to be siphoned into the sampling bottle. After sampling—each bottle typically being half full—the sidearm was filled again with seawater and capped until analysis. All gas samples were analyzed within 4 months of sampling.&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;Before gas analysis, bottles were gently agitated on a shaker table for 48h to equilibrate dissolved gases with the&amp;amp;nbsp;&amp;lt;br /&amp;gt;
headspace at room temperature (25C). Next, bottles were inverted and the seawater pumped out. Finally, the headspace gases were extracted and purified according to Li et al. (2019), Yeung et al. (2016), and Yeung et al. (2018), in which O2 is separated from Ar and N2 by gas chromatography. O2/Ar ratios are standardized relative to atmospheric O2 and air dissolved in distilled water. Bulk δ18O and 17Δ values are standardized against atmospheric O2 and O2 derived from laser-fluorination of San Carlos Olivine (Yeung et al. 2018). Clumped-isotope Δ35 and Δ36 values are standardized against laboratory-generated photolytic and heated-gas standards (Yeung et al. 2014).&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;O2/Ar ratios were determined by integrating the peak areas for each species on an Aglient 7890B gas chromatograph utilizing thermal conductivity detection. Dissolved O2 saturation was determined from these O2/Ar measurements and checked independently through manometric determination of O2 yield and weighing the seawater from which it was extracted. Isotopologue analyses were performed on a custom Nu Instruments Perspective IS high-resolution isotope ratio mass spectrometer at Rice University.&amp;lt;br /&amp;gt;
&amp;lt;br /&amp;gt;
Data was processed as was done in Yeung et al. (2018) for δ18O and 17Δ values and Yeung et al. (2016) for clumped-isotope values. Dissolved oxygen saturation is calculated using potential temperature and salinity and the O2 and Ar saturation calculated using MATLAB programs by Roberta Hamme (O2sol and Arsol from https://web.uvic.ca/~rhamme/download.html). These calculated values were compared to measured values to determine O2/O2sat.&amp;lt;/p&amp;gt;</gco:CharacterString>
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        <gmx:Anchor xlink:href="http://lod.bco-dmo.org/id/award/750417.rdf" xlink:title="OCE-1436590" xlink:actuate="onRequest">Funding provided by NSF Division of Ocean Sciences (NSF OCE) Award Number: OCE-1436590 Award URL: https://www.nsf.gov/awardsearch/show-award?AWD_ID=1436590</gmx:Anchor>
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        <gmx:Anchor xlink:href="http://lod.bco-dmo.org/id/award/750424.rdf" xlink:title="OCE-1533501" xlink:actuate="onRequest">Funding provided by NSF Division of Ocean Sciences (NSF OCE) Award Number: OCE-1533501 Award URL: https://www.nsf.gov/awardsearch/show-award?AWD_ID=1533501</gmx:Anchor>
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        <gmx:Anchor xlink:href="http://lod.bco-dmo.org/id/award/750426.rdf" xlink:title="OCE-1436326" xlink:actuate="onRequest">Funding provided by NSF Division of Ocean Sciences (NSF OCE) Award Number: OCE-1436326 Award URL: https://www.nsf.gov/awardsearch/show-award?AWD_ID=1436326</gmx:Anchor>
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        <gmx:Anchor xlink:href="http://lod.bco-dmo.org/id/award/750436.rdf" xlink:title="OCE-1559004" xlink:actuate="onRequest">Funding provided by NSF Division of Ocean Sciences (NSF OCE) Award Number: OCE-1559004 Award URL: https://www.nsf.gov/awardsearch/show-award?AWD_ID=1559004</gmx:Anchor>
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        <gmx:Anchor xlink:href="http://lod.bco-dmo.org/id/award/750441.rdf" xlink:title="OCE-1559215" xlink:actuate="onRequest">Funding provided by NSF Division of Ocean Sciences (NSF OCE) Award Number: OCE-1559215 Award URL: https://www.nsf.gov/awardsearch/show-award?AWD_ID=1559215</gmx:Anchor>
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Ocean acidification (OA) is the decrease in seawater pH due to increased oceanic uptake of anthropogenic carbon dioxide (CO2) from the atmosphere. The impact of this uptake in the marine environment is lessened by the dissolution of calcium carbonate (CaCO3) to calcium and carbonate ions, allowing carbonate ions to bind free hydrogen ions that cause the decrease in pH. Researchers from the University of Southern California and California Institute of Technology have developed a new method for determining carbonate dissolution rates that work in both laboratory and field settings. Preliminary data using this technique has revealed a distinct difference in measured rates between those obtained in the laboratory and those in the field. It is crucial that laboratory and field measurements be standardized to be able to accurately study and compare dissolution rate studies. As such, the researchers will perform extensive fieldwork and laboratory to bridge the gap between these dissolution rate measurements. Results will be widely useful to the ocean chemistry community, especially modelers, wishing to study any aspect of ocean carbonate chemistry, as well as paleoceanographers using carbonate material to study past ocean conditions. Graduate students will be co-mentored by the researchers, and the University of Southern California's (USC) Young Researcher Program will allow the researchers to involve local high school students. USC International Relations students will be involved in the project, not only gaining scientific experience, but also will learn the policy aspect of the science.&lt;/p&gt;
&lt;p&gt;Calcium carbonate (CaCO3) dissolution helps to mitigate the effects of ocean acidification (OA) and is a key factor in the ocean's alkalinity balance. The researchers have recently developed a novel tracer methodology which can monitor carbonate dissolution rates in both the lab and field. This method traces the transfer of 13C from labeled solids to seawater. Using this method has led to breakthroughs in understanding the controls of CaCO3 dissolution kinetics, but it has also revealed that the measurements made in a lab and in the field are not entirely in line. It is crucial to be able to correlate these two measurements to be able to fully study and understand the dynamics of CaCO3 dissolution. Therefore, the researchers will extend their previous work to standardize the results of measurements in the lab with those in the ocean. The North Pacific Ocean with a gradient in carbonate saturation states will be used for the field study, and lab-based experiments will allow the researchers to constrain variables such as pressure, the dissolved inorganic carbon/alkalinity ratio, and concentrations of phosphate. This research will further understanding of OA, the mechanisms controlling carbonate dissolution, and how the ocean modulates its alkalinity budget.&lt;/p&gt;</gco:CharacterString>
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