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            <gmx:Anchor xlink:href="http://lod.bco-dmo.org/id/dataset/931843.rdf" xlink:actuate="onRequest">Biogenic and lithogenic silica concentrations from marine suspended particles collected during the 2011 CLIVAR S04P expedition on RVIB Nathaniel B. Palmer from February 19 to April 19, 2011</gmx:Anchor>
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            <gco:CharacterString>Cite this dataset as: Morton, P. L., Krause, J. W. (2025) Biogenic and lithogenic silica concentrations from marine suspended particles collected during the 2011 CLIVAR S04P expedition on RVIB Nathaniel B. Palmer from February 19 to April 19, 2011. Biological and Chemical Oceanography Data Management Office (BCO-DMO). (Version 1) Version Date 2025-09-03 [if applicable, indicate subset used]. doi:10.26008/1912/bco-dmo.931843.1 [access date]</gco:CharacterString>
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        <gco:CharacterString>Biogenic and lithogenic silica in Southern Ocean marine suspended particulate material (0-1000 m) Dataset Description:  Methods and Sampling: &amp;lt;p&amp;gt;Water (2-10.9 liters) from each GO-Flo was filtered over a 47-millimeter (mm) diameter, 0.4-micrometer (µm) pore size PCTE filter (Measures et al., 2008). Samples were stored in new Whatman petri slides, double-bagged, at room temperature until ready for processing. The filters were subdivided into thirds or quarters using a ceramic rotary blade on a clean acrylic panel.&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;One subsection (1/3 or 1/4) was processed for biogenic and lithogenic silica concentrations, according to Krause et al. (2009) and Brzezinski and Nelson (1995). In brief, the filter subsample was submerged in 0.2 N NaOH for 2 hours in Teflon tubes to dissolve the silica. The resulting solution was reacted with ammonium molybdate, metol, and oxalic acid to produce silicomolybous acid, the absorbance of which was measured spectrophotometrically.&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;Lithogenic silica concentrations were determined using a subsample of the original NaOH digest solution, which was diluted with DI water and centrifuged. The supernatant was taken to dryness then digested again using HF over 48 hours. Boric acid was added to the HF solution, which was then reacted and analyzed in the same way as the biogenic silica digest solutions.&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;Concentrations were determined using matrix-matched standards for both the biogenic and lithogenic digest solutions.&amp;lt;/p&amp;gt;</gco:CharacterString>
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        <gmx:Anchor xlink:href="http://lod.bco-dmo.org/id/award/752515.rdf" xlink:title="OCE-1658311" xlink:actuate="onRequest">Funding provided by NSF Division of Ocean Sciences (NSF OCE) Award Number: OCE-1658311 Award URL: https://www.nsf.gov/awardsearch/show-award?AWD_ID=1658311</gmx:Anchor>
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Better documenting the record of rapid climate changes and the mechanisms for these events, and evaluating the potential for abrupt climate changes in the future;
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Detecting and describing any climate changes that may occur.

Program Data: The data from most projects associated with the US CLIVAR program are not managed by BCO-DMO. Information about these projects and their results are available from the Program and Data site URLs shown above. However, there are a few exceptions, and those projects are listed below when the project section is expanded.</gco:CharacterString>
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Ocean research over the last several decades has increasingly shown the great importance of iron chemistry on marine biological processes. In certain areas of the ocean where iron is scarce, it can limit biological growth even though other essential nutrients like nitrogen and phosphorus are abundant. Consequently, to fully understand and quantify biological productivity in the ocean, a complete knowledge of all sources and sinks for iron is essential. The researchers funded for this project have already generated exciting preliminary data that suggest a potentially large, yet, unquantified pathway for iron removal. Diatoms, phytoplankton with shells made of silica, are shown to incorporate traces of iron into their shells, making it unavailable for rapid recycling or use by marine organisms in surface waters. Given the great abundance of diatoms in many parts of the ocean, this could represent a major, unstudied removal mechanism that regulates the concentration of iron in seawater. This research could transform current understanding of how iron is removed from the ocean, and it will impact understanding of both the chemical and biological processes involving iron in seawater. The investigator also plans outreach in K-12 schools by providing educational courses for Earth Science teachers and will support graduate student training in advanced chemical analysis and oceanography.&lt;/p&gt;
&lt;p&gt;High-resolution synchrotron-based chemical techniques will allow determination of the concentration and oxidation state of iron bound within diatom frustules. This analytical advance has created the ability for unique evaluation of iron sequestration into biogenic silica as a major pathway for iron removal from the ocean. Samples from the Pacific sector of the Southern Ocean have been collected in a previous CLIVAR field campaign and a subset of these are available for new synchrotron analysis of iron (Fe) with Near Edge X-ray Fluorescence Spectroscopy (Fe-NEXFS) and submicron scale X-ray fluorescence mapping, as well as a variety of other chemical characterizations. With these methods, the project will determine the importance of iron sequestered into biogenic silica as a new and unquantified loss term in the oceanic Fe cycle and examine the changing chemical complexes of iron during vertical transport of silica particles through the water column.&lt;/p&gt;</gco:CharacterString>
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&amp;lt;p&amp;gt;One subsection (1/3 or 1/4) was processed for biogenic and lithogenic silica concentrations, according to Krause et al. (2009) and Brzezinski and Nelson (1995). In brief, the filter subsample was submerged in 0.2 N NaOH for 2 hours in Teflon tubes to dissolve the silica. The resulting solution was reacted with ammonium molybdate, metol, and oxalic acid to produce silicomolybous acid, the absorbance of which was measured spectrophotometrically.&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;Lithogenic silica concentrations were determined using a subsample of the original NaOH digest solution, which was diluted with DI water and centrifuged. The supernatant was taken to dryness then digested again using HF over 48 hours. Boric acid was added to the HF solution, which was then reacted and analyzed in the same way as the biogenic silica digest solutions.&amp;lt;/p&amp;gt;

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- Added DATE column from the bottle file; joining data by station number.
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