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            <gco:CharacterString>Cite this dataset as: Doherty, S. C., Christensen, S., Davis, C. V., McCarthy, M. D. (2025) Compound-specific carbon stable isotopes of amino acids in planktic foraminifera from Santa Barbara Basin sediment traps from 2018 to 2021. Biological and Chemical Oceanography Data Management Office (BCO-DMO). (Version 1) Version Date 2025-11-26 [if applicable, indicate subset used]. doi:10.26008/1912/bco-dmo.986825.1 [access date]</gco:CharacterString>
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        <gco:CharacterString>Carbon CSI-AA SBB trap foraminifera Dataset Description:  Methods and Sampling: &amp;lt;p&amp;gt;Samples were collected using a McLane Parflux 78H sediment trap deployed at depths &amp;amp;gt;400 meters (m) in the central Santa Barbara Basin (34.2450389, -120.0592917). The sampling interval was 10 to 14 days, and samples were preserved in borate-buffered formalin solution. A 1/16th split of the sediment trap sample was used. Samples were rinsed with tap water over a 125-micron sieve, and foraminifera tests were removed from other trap material using a fine paintbrush. Foraminifera tests were dried on a micropaleontology slide, then species were identified by test morphology and sorted. Tests of the three most abundant species were removed to separate micropaleontology slides. These tests were inspected under a dissecting microscope to ensure no organic particles were adhered to the exterior or interior of tests. Any organic particles were gently removed with a wet brush. The removed tests were counted and weighed on a microbalance. Tests from multiple sediment trap samples were combined to achieve a sample of 5-10 milligrams (mg). This combined sample was gently rinsed with methanol three times, then dried.&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;Compound-specific stable isotopes were measured at the UC Santa Cruz Stable Isotope Lab. Tests were demineralized by adding ~1 milliliter (mL) 1N HCl to dissolve carbonate, then stored at 4 degrees Celsius (°C) overnight to complete the demineralization reaction. The HCl was then evaporated under N&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;. The remaining organic matter was then hydrolyzed with ~ 1mL 6N HCl at 110°C for 20 hours after the vial was purged with N&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt; to remove oxygen. Samples were purified by cation-exchange chromatography with DOWEX 50WX8-400 resin. Amino acids were measured as trifluoroacetyl isopropyl ester derivatives following Silfer et al. (1991). After drying under N&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;, samples were esterified with a 1:5 mixture of acetyl chloride:isopropanol at 110 °C for 60 minutes. Samples were dried again under N&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;, then trifluoroacetylation was completed using a 1:3 mixture of trifluoroacetic anhydride (TFAA) and dichloromethane (DCM) at 110 °C for 15 minutes. Inorganic salts were removed from samples by liquid-liquid extraction of derivatized amino acids in chloroform and an aqueous phosphate buffer. Trifluoroacetylation was completed again after liquid-liquid extraction. Samples were dried and dissolved in ethyl acetate for gas chromatography-isotope ratio mass spectrometry (GC-IRMS).&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;Amino acid stable isotopes were measured on a Thermo 1310 Trace gas chromatograph coupled to an Isolink II (Thermo combustion reactor 1000°C), Conflo IV, and Thermo Delta V Plus IRMS at the UCSC-SIL. Amino acids were separated for δ15N analyses using a BPX5 column (60 m×0.32 mm, 1 μm film thickness; SGE Analytical Science, Trajan, Austin, TX, USA) and for δ13C analyses using a DB-5 column (50 m× 0.32 mm 0.52 μm film thickness; Agilent Technologies, Santa Clara, CA, USA). Samples were analyzed alongside a set of amino acid standards of known δ13C and δ15N values. The injector temperature was 250°C with He column flow rate of 2 mL/min. The GC temperature program for carbon isotope analysis was: initial temp = 75°C hold for 2 min; ramp 1 = 4°C/min to 90°C, hold for 4 min; ramp 2 = 4°C/min to 185°C, hold for 5 min; ramp 3 = 10°C/min to 250°C, hold for 2 min; ramp 4 = 20°C/min to 300°C, hold for 5 min.&amp;lt;/p&amp;gt;</gco:CharacterString>
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        <gmx:Anchor xlink:href="http://lod.bco-dmo.org/id/award/982733.rdf" xlink:title="OCE-2303608" xlink:actuate="onRequest">Funding provided by NSF Division of Ocean Sciences (NSF OCE) Award Number: OCE-2303608 Award URL: https://www.nsf.gov/awardsearch/show-award?AWD_ID=2303608</gmx:Anchor>
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Current climate change is unique in human history. To understand how the Earth and life on it responds to comparable change it is necessary to look millions of years in the past. A huge amount of what we know about past climate comes from the fossils of marine plankton. Specifically, a group of single-celled organisms called foraminifera. Foraminifera make tiny fossil shells which capture the chemistry of the water they grew in. As a result, they can be used to reconstruct ancient ocean waters and climate. To use the fossil shells of foraminifera to their greatest effect, the ecology of the living creature must be understood. Variables like what the foraminifera ate, what depth it lived at, and whether it had symbionts will all impact how shell chemistry is interpreted. Compound-specific nitrogen and carbon isotopes of specific amino acids (CSI-AA) represent a unique approach to study these variables in living plankton. This proposal would test how well this approach can be applied to fossil shells. If successful, this would provide powerful ways to describe the ecology of long extinct planktic foraminifera. In doing so, one may better understand the records they hold of Earth’s past. The project broader impacts include support for a postdoctoral researcher, development of a career-opportunities workshop to introduce students from Primarily Undergraduate Institutions to geoscience research, and content contributions to a summer program for at-risk STEM transfer students at UC Santa Cruz.&lt;/p&gt;
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&amp;lt;p&amp;gt;Compound-specific stable isotopes were measured at the UC Santa Cruz Stable Isotope Lab. Tests were demineralized by adding ~1 milliliter (mL) 1N HCl to dissolve carbonate, then stored at 4 degrees Celsius (°C) overnight to complete the demineralization reaction. The HCl was then evaporated under N&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;. The remaining organic matter was then hydrolyzed with ~ 1mL 6N HCl at 110°C for 20 hours after the vial was purged with N&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt; to remove oxygen. Samples were purified by cation-exchange chromatography with DOWEX 50WX8-400 resin. Amino acids were measured as trifluoroacetyl isopropyl ester derivatives following Silfer et al. (1991). After drying under N&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;, samples were esterified with a 1:5 mixture of acetyl chloride:isopropanol at 110 °C for 60 minutes. Samples were dried again under N&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;, then trifluoroacetylation was completed using a 1:3 mixture of trifluoroacetic anhydride (TFAA) and dichloromethane (DCM) at 110 °C for 15 minutes. Inorganic salts were removed from samples by liquid-liquid extraction of derivatized amino acids in chloroform and an aqueous phosphate buffer. Trifluoroacetylation was completed again after liquid-liquid extraction. Samples were dried and dissolved in ethyl acetate for gas chromatography-isotope ratio mass spectrometry (GC-IRMS).&amp;lt;/p&amp;gt;

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            <gco:CharacterString>PI Supplied Instrument Name: Thermo 1310 Trace gas chromatograph coupled to an Isolink II and Conflo IV PI Supplied Instrument Description:Amino acid stable isotopes were measured on a Thermo 1310 Trace gas chromatograph coupled to an Isolink II (Thermo combustion reactor 1000°C), Conflo IV, and Thermo Delta V Plus IRMS at the UCSC-SIL. Instrument Name: Gas Chromatograph Mass Spectrometer Instrument Short Name:   Instrument Description: Instruments separating gases, volatile substances or substances dissolved in a volatile solvent by transporting an inert gas through a column packed with a sorbent to a detector for assay by a mass spectrometer.</gco:CharacterString>
          </gmi:description>
        </gmi:MI_Instrument>
      </gmi:instrument>
      <gmi:instrument>
        <gmi:MI_Instrument>
          <gmi:identifier>
            <gmd:MD_Identifier>
              <gmd:code>
                <gmx:Anchor xlink:href="http://lod.bco-dmo.org/id/instrument/469.rdf" xlink:title="Isotope-ratio Mass Spectrometer" xlink:actuate="onRequest">Thermo Delta V Plus IRMS</gmx:Anchor>
              </gmd:code>
            </gmd:MD_Identifier>
          </gmi:identifier>
          <gmi:type>
            <gco:CharacterString>Thermo Delta V Plus IRMS</gco:CharacterString>
          </gmi:type>
          <gmi:description>
            <gco:CharacterString>PI Supplied Instrument Name: Thermo Delta V Plus IRMS PI Supplied Instrument Description:Amino acid stable isotopes were measured on a Thermo 1310 Trace gas chromatograph coupled to an Isolink II (Thermo combustion reactor 1000°C), Conflo IV, and Thermo Delta V Plus IRMS at the UCSC-SIL. Instrument Name: Isotope-ratio Mass Spectrometer Instrument Short Name:IR Mass Spec; IRMS   Instrument Description: The Isotope-ratio Mass Spectrometer is a particular type of mass spectrometer used to measure the relative abundance of isotopes in a given sample (e.g. VG Prism II Isotope Ratio Mass-Spectrometer). Community Standard Description: http://vocab.nerc.ac.uk/collection/L05/current/LAB16/</gco:CharacterString>
          </gmi:description>
        </gmi:MI_Instrument>
      </gmi:instrument>
      <gmi:instrument>
        <gmi:MI_Instrument>
          <gmi:identifier>
            <gmd:MD_Identifier>
              <gmd:code>
                <gmx:Anchor xlink:href="http://lod.bco-dmo.org/id/instrument/708.rdf" xlink:title="Microscope - Optical" xlink:actuate="onRequest">dissecting microscope</gmx:Anchor>
              </gmd:code>
            </gmd:MD_Identifier>
          </gmi:identifier>
          <gmi:type>
            <gco:CharacterString>dissecting microscope</gco:CharacterString>
          </gmi:type>
          <gmi:description>
            <gco:CharacterString>PI Supplied Instrument Name: dissecting microscope PI Supplied Instrument Description:Tests were inspected under a dissecting microscope. Instrument Name: Microscope - Optical Instrument Short Name:   Instrument Description: Instruments that generate enlarged images of samples using the phenomena of reflection and absorption of visible light. Includes conventional and inverted instruments. Also called a &quot;light microscope&quot;. Community Standard Description: http://vocab.nerc.ac.uk/collection/L05/current/LAB05/</gco:CharacterString>
          </gmi:description>
        </gmi:MI_Instrument>
      </gmi:instrument>
      <gmi:instrument>
        <gmi:MI_Instrument>
          <gmi:identifier>
            <gmd:MD_Identifier>
              <gmd:code>
                <gmx:Anchor xlink:href="http://lod.bco-dmo.org/id/instrument/518.rdf" xlink:title="Sediment Trap" xlink:actuate="onRequest">McLane PARFLUX 78HW-13 sediment trap</gmx:Anchor>
              </gmd:code>
            </gmd:MD_Identifier>
          </gmi:identifier>
          <gmi:type>
            <gco:CharacterString>McLane PARFLUX 78HW-13 sediment trap</gco:CharacterString>
          </gmi:type>
          <gmi:description>
            <gco:CharacterString>PI Supplied Instrument Name: McLane PARFLUX 78HW-13 sediment trap PI Supplied Instrument Description:A McLane PARFLUX 78HW-13 sediment trap was used to collect samples. Instrument Name: Sediment Trap Instrument Short Name:Sediment Trap   Instrument Description: Sediment traps are specially designed containers deployed in the water column for periods of time to collect particles from the water column falling toward the sea floor. In general a sediment trap has a jar at the bottom to collect the sample and a broad funnel-shaped opening at the top with baffles to keep out very large objects and help prevent the funnel from clogging. This designation is used when the specific type of sediment trap was not specified by the contributing investigator. Community Standard Description: http://vocab.nerc.ac.uk/collection/L05/current/33/</gco:CharacterString>
          </gmi:description>
        </gmi:MI_Instrument>
      </gmi:instrument>
      </gmi:MI_AcquisitionInformation>
  </gmi:acquisitionInformation>
</gmi:MI_Metadata>
