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            <gmx:Anchor xlink:href="http://lod.bco-dmo.org/id/dataset/808834.rdf" xlink:actuate="onRequest">Underway/continuous measurements of O2, O2/Ar and optically-based POC in the North Pacific from 2017-09-05 to 2017-09-27</gmx:Anchor>
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            <gco:CharacterString>Cite this dataset as: White, A. E., Quay, P. (2020) Underway/continuous measurements of O2, O2/Ar and optically-based POC in the North Pacific from 2017-09-05 to 2017-09-27. Biological and Chemical Oceanography Data Management Office (BCO-DMO). Version Date 2020-04-09 [if applicable, indicate subset used]. http://lod.bco-dmo.org/id/dataset/808834 [access date]</gco:CharacterString>
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        <gco:CharacterString>Underway/continuous measurements of O2, O2/Ar and optically-based POC in the North Pacific Dataset Description: &amp;lt;p&amp;gt;The cruise (KM1713) transited from Seward, AK to Honolulu, HI from 3-26 September 2017 onboard the R/V Kilo Moana. Six extended stations (Stn), three in subpolar waters (Stn 1 at 55°N, Stn 2 at 50°N, and Stn 3 at 46°N), one in the transition zone between subpolar and subtropical waters (Stn 4 at 42°N), and two in the subtropical gyre (Stn 5 at 34°N, and Stn 6 at 24°N) were occupied for 2-3 day periods during which continuous measurements of conductivity, temperature, O2, O2/Ar and beam attenuation were measured continuously on surface seawater supplied via the ships’ intake line and using CTD profiles of conductivity, temperature, pressure, oxygen, and the particulate beam attenuation coefficient conducted at ~2-hr intervals. An autonomous profiling float was deployed for ~ 2 days at four stations, retrieving CTD and oxygen profiles at approximately 3-hour intervals. Another float with same mission design was deployed near station ALOHA (22.45° N, 158° W) during July 2017 to provide mixed-layer averaged O2 near station 6. When available, the ship followed the trajectory of the profiling float, yielding a near-Lagrangian sampling strategy with the aim to minimize horizontal mixing effects.&amp;lt;/p&amp;gt; Methods and Sampling: &amp;lt;p&amp;gt;&amp;lt;strong&amp;gt;Underway/continuous measurements of O2, O2/Ar and optically-based POC&amp;lt;/strong&amp;gt;&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;Continuous measurements of surface O2, O2/Ar, POC, and beam attenuation coefficients used seawater supplied from an uncontaminated seawater intake line located at ~7m depth.&amp;amp;nbsp; All continuous measurements were binned into hourly averages at each station. Continuous measurements of dissolved O2 concentration using an Optode (Aanderaa) and the dissolved O2/Ar&amp;amp;nbsp; gas ratios using an equilibrator inlet mass spectrometer (EIMS) system [Cassar et al., 2009] were obtained at each station. Dissolved oxygen data (Optode) were corrected for pressure and salinity following Uchida et al. [2008]. O2/Ar measured by the EIMS were calibrated to O2/Ar measurements by mass spectrometer on discrete water samples collected in the mixed layer during the cruise (n=58). Saturated O2 concentrations and O2/Ar values were calculated using the solubility equations of García and Gordon [1992] for O2 and Hamme and Emerson [2004] for Ar. Diurnal changes in O2/Ar data measured by the EIMS instrument were corrected for fluctuations in total gas pressure based on concurrent changes in N2/Ar, yielding O2/Ar*, (i.e., % deviation in O2/Ar* = % deviation O2/Ar – a*% deviation N2/Ar, where ‘a’ represents a calibration factor between N2/Ar and O2/Ar deviations determined at each station). Diurnal changes in O2 were determined by multiplying the relative deviation from the mean O2 measured by the Optode by the mean surface Winkler O2 concentration measured at each station (Eq. 1), where i refers to each datapoint in time, and overbars denotes the mean values while on each station. The diurnal changes in O2/Ar and O2/Ar* were calibrated to Winkler concentrations using the same procedure.&amp;lt;/p&amp;gt;

&amp;lt;div&amp;gt;Continuous measurements of the beam attenuation coefficient (660 nm) were obtained with a C-Star instrument (Sea-Bird Scientific).&amp;amp;nbsp; A debubbler and a valve control device were used to divert water to a 0.2 μm membrane filter for the first 10 minutes of every hour to provide background estimates of beam attenuation due to water and dissolved substances [Slade et al., 2010]. These blank values were linearly interpolated throughout the cruise and subtracted from the raw measurements to provide particulate beam attenuation coefficient (cp, m-1).&amp;amp;nbsp;&amp;lt;/div&amp;gt;

&amp;lt;p&amp;gt;Discrete water samples (collected on combusted GF/F filters with filter blank corrections following the Hawaiian&amp;amp;nbsp;Ocean Time Series (HOT) protocols, http://hahana.soest.hawaii.edu/hot/methods/pcpn.html) were collected from the ship’s uncontaminated seawater system to determine particulate organic carbon (POC) concentrations every ~2.5 hours (n=107 in total) using a semi-automated filtration device [based on the design of Holser et al., 2011]. Underway POC were scaled to mean near-surface (&amp;amp;lt;10 m) samples collected at each station (n=12; r2=0.92) and these corrected values were then used to convert cp measurements to POC using Eq. 2, where&amp;amp;nbsp; is the mean in situ POC measured at each station.&amp;lt;/p&amp;gt;</gco:CharacterString>
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        <gmx:Anchor xlink:href="http://lod.bco-dmo.org/id/award/792395.rdf" xlink:title="OCE-1849012" xlink:actuate="onRequest">Funding provided by NSF Division of Ocean Sciences (NSF OCE) Award Number: OCE-1849012 Award URL: https://www.nsf.gov/awardsearch/show-award?AWD_ID=1849012</gmx:Anchor>
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        <gmx:Anchor xlink:href="http://lod.bco-dmo.org/id/award/792400.rdf" xlink:title="OCE-1536121" xlink:actuate="onRequest">Funding provided by NSF Division of Ocean Sciences (NSF OCE) Award Number: OCE-1536121 Award URL: https://www.nsf.gov/awardsearch/show-award?AWD_ID=1536121</gmx:Anchor>
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Source: Department of Geosciences, Princeton University, Princeton, New Jersey 08544, USA. ncassar@princeton.edu

Abstract
The oxygen (O(2)) concentration in the surface ocean is influenced by biological and physical processes. With concurrent measurements of argon (Ar), which has similar solubility properties as oxygen, we can remove the physical contribution to O(2) supersaturation and determine the biological oxygen supersaturation. Biological O(2) supersaturation in the surface ocean reflects the net metabolic balance between photosynthesis and respiration, i.e., the net community productivity (NCP). We present a new method for continuous shipboard measurements of O(2)/Ar by equilibrator inlet mass spectrometry (EIMS). From these measurements and an appropriate gas exchange parametrization, NCP can be estimated at high spatial and temporal resolution. In the EIMS configuration, seawater from the ship's continuous intake flows through a cartridge enclosing a gas-permeable microporous membrane contactor. Gases in the headspace of the cartridge equilibrate with dissolved gases in the flowing seawater. A fused-silica capillary continuously samples headspace gases, and the O(2)/Ar ratio is measured by mass spectrometry. The ion current measurements on the mass spectrometer reflect the partial pressures of dissolved gases in the water flowing through the equilibrator. Calibration of the O(2)/Ar ion current ratio (32/40) is performed automatically every 2 h by sampling ambient air through a second capillary. A conceptual model demonstrates that the ratio of gases reaching the mass spectrometer is dependent on several parameters, such as the differences in molecular diffusivities and solubilities of the gases. Laboratory experiments and field observations performed by EIMS are discussed. We also present preliminary evidence that other gas measurements, such as N(2)/Ar and pCO(2) measurements, may potentially be performed with EIMS. Finally, we compare the characteristics of the EIMS with the previously described membrane inlet mass spectrometry (MIMS) approach.

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