Fe(II) was measured shipboard on the GEOTRACES GP17 (NBP2401) cruise within an hour of collection. Samples were collected from cores obtained by multicoring and from the water column using a trace metal clean rosette. Samples were analyzed by chemiluminescence, utilizing the oxidation of luminol, which is catalyzed by Fe(II). Most samples were collected within the Amundsen Sea Polynya, near the sediment water interface and in surface waters containing a large Phaeocystis bloom. Significant eleva...
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All reagents were prepared in acid-washed opaque low-density polyethylene (LDPE) bottles, to prevent trace metal contamination or degradation of the reagents by light. The luminol reagent was initially prepared as a concentrate, by mixing 0.796 grams (g) sodium luminol (Sigma), 250 milliliters (mL) Optima grade ammonium hydroxide solution (Fisher), high-purity water (18.2 megohms per centimeter (MΩ cm⁻¹)), and approximately 45 mL Optima grade hydrochloric acid (Fisher) to reach a final volume of 1 liter (L) and a pH of 10.25. To produce the working reagent, the concentrated mixture was diluted in high-purity water by a factor of four and heated at 50 degrees Celsius (°C) for 9 to 12 hours in either an oven or a hot water bath. DTPA was prepared in high-purity water with final concentrations of 50 millimolar (mM) DTPA (Sigma-Aldrich) and 200 mM NaOH (Aldrich, trace metals basis). EDTA was prepared in high-purity water with a final concentration of 50 mM EDTA (Aldrich, trace metals basis) and 100 mM NaOH (Aldrich, trace metals basis). The MOPS (3-(N-Morpholino)propanesulfonic acid) buffer was prepared with a final concentration of 100 mM MOPS (Sigma) and 50 mM NaOH (Aldrich, trace metals basis) in high-purity water, so that the final pH was 7.2. All reagents were used within 1 month of preparation.
Because iron(II) oxidizes rapidly in seawater, standards were prepared individually and analyzed immediately. A primary stock of 10⁻² M Fe(II) was prepared by dissolving ammonium iron(II) sulfate in high-purity water acidified to pH 2 using Optima grade hydrochloric acid (Fisher). The low pH slows oxidation to negligible levels, but the standard was replaced monthly. A working stock was prepared by diluting the primary stock by a factor of 10⁴ in high purity, creating a 10⁻⁶ M solution at pH 6. This solution would oxidize to a significant extent within several hours, so it was always prepared fresh immediately before a calibration curve or an experiment using standards. This working stock was then added to iron(II) free seawater, acquired by filtering seawater through a 0.2 micrometer (μm) filter and storing in an opaque bottle at room temperature for at least 24 hours.
Dissolved iron(II) concentrations were measured using a luminol chemiluminescence-based FeLume flow-injection system (Waterville Analytical), with data collection and integration controlled by Waterville Analytical software. The hardware was similar to that used in a number of previous open-ocean studies. A standard quartz flow cell was used in conjunction with a Hamamatsu HC135 photon counter. The flow rate through the peristaltic pump was 2 milliliters per minute (mL min⁻¹). The photon counter integration time was 200 milliseconds (ms), with two measurements per second for up to 360 seconds. All samples were introduced in acid-washed Teflon bottles.
Moffett, J. W., Floback, A. (2025) Fe(II) measured shipboard on the GP17-ANT RVIB Palmer cruise NBP24-01 in the Amundsen Sea from November 2023 to January 2024. Biological and Chemical Oceanography Data Management Office (BCO-DMO). (Version 1) Version Date 2025-08-19 [if applicable, indicate subset used]. http://lod.bco-dmo.org/id/dataset/982741 [access date]
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