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OAS accession Detail for 0291594, meta_version: 1. Current meta_version is: 1
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| accessions_id: | 0291594 | archive |
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| Title: | Dissolved Gallium (Ga) from R/V Thomas G. Thompson cruise TN303 (GP16) in the Eastern Tropical Pacific in 2013 (U.S. GEOTRACES EPZT project) (NCEI Accession 0291594) |
| Abstract: | This dataset contains chemical and physical data collected on R/V Thomas G. Thompson during cruise TN303 in the South Pacific Ocean from 2013-10-28 to 2013-12-17. These data include Gallium and depth. The instruments used to collect these data include GO-FLO Teflon Trace Metal Bottle, GeoFish Towed near-Surface Sampler, and Inductively Coupled Plasma Mass Spectrometer. These data were collected by Alan M. Shiller of University of Southern Mississippi as part of the "Geotraces Pacific Section: Gallium, vanadium, and associated elements indicative of dust input and redox cycling (EPZT_Ga_V_others)" and "U.S. GEOTRACES East Pacific Zonal Transect (U.S. GEOTRACES EPZT)" projects and "U.S. GEOTRACES (U.S. GEOTRACES)" program. The Biological and Chemical Oceanography Data Management Office (BCO-DMO) submitted these data to NCEI on 2021-01-07. The following is the text of the dataset description provided by BCO-DMO: Dissolved Gallium (Ga) from R/V Thomas G. Thompson cruise TN303 (GP16) in the Eastern Tropical Pacific in 2013 (U.S. GEOTRACES EPZT project) Dataset Description: Acquisition Description: Clean seawater samples were collected from two sources; a GEOTRACES CTD referred to as GT-C/12L GoFlo, and the Super-GeoFISH towed surface vehicle. For more information on these methods, see the cruise report and the GeoFish Instrument Description. Water column samples were filtered through pre-cleaned, 0.2 μm Pall Acropak Supor filter capsules as described elsewhere (e.g., Cutter & Bruland 2012; Hatta et al., 2015). Near surface water samples were collected using an underway towed-fish pumped seawater system (Bruland et al., 2005) with samples filtered through sequential 0.45 μm Osmonics and 0.2 μm Polycarbonate (PCTE) cartridge filters. Filtered water was collected in 125 mL HDPE bottles (Nalgene) that had been precleaned by soaking in hot 1.2 M HCl (reagent grade) for at least 8 h with subsequent thorough rinsing with ultrapure distilled deionized water (Barnstead E-pure). Samples were acidified in a laminar flow bench aboard ship using 0.5 mL of ultrapure HCl per 125 mL sample. Dissolved Ga was determined by isotope dilution ICP-MS using a ThermoFisher Element 2 operated in low resolution. Samples were concentrated using Mg(OH)₂ co-precipitation (e.g., Shiller & Bairamadgi, 2006; Zurbrick et al., 2012). Briefly, in this technique, a small addition (~70 μL) of clean aqueous ammonia is added to the acidified seawater sample (~7.5 mL) which precipitates a fraction of the dissolved magnesium as the hydroxide, which in turn, scavenges the gallium from solution. An enriched isotope spike of known concentration was prepared using purified enriched ⁷¹Ga (99.8%), obtained from Oak Ridge National Laboratories. Because there is a significant interference of doubly charged ¹³⁸Ba with ⁶⁹Ga, the precipitate was washed three times with a solution of high purity 0.1% NH₄OH to minimize residual Ba. The precipitate was then dissolved in 550 mL ultrapure 3% HNO3 (Seastar Chemicals, Baseline) and analyzed in low resolution using a ThermoFinnigan Element 2 High Resolution Inductively Coupled Plasma Mass Spectrometer (HR-ICP-MS). Isotopes monitored on the ICP-MS were ⁶⁹Ga, ⁷¹Ga, and ¹³⁸Ba. A slight correction for residual Ba was made based on the ratio of responses at masses 69 and 138 to a Ba standard solution. Because the residual salt content varied from sample to sample, it was not possible to matrix-match the Ba correction standard. However, typically, this correction affected the final result by The reagent blank contribution to the dissolved Ga analysis is typically 0.6 pmol/kg and the detection limit (based on 3 times the standard deviation of the blank) is 0.3 pmol/kg. Repeated runs of US GEOTRACES intercalibration samples (GS and GD) and in-house reference solutions suggest a precision of +/- 4.0%; the limit of detection for Ga was 1.5 pmol/kg. Recovery of the method, as determined by repeated analysis of a spiked and unspiked seawater sample was 101.3 +/- 4.7%. |
| Date received: | 20210107 |
| Start date: | 20131028 |
| End date: | 20131217 |
| Seanames: | South Pacific Ocean |
| West boundary: | -152.079 |
| East boundary: | -77.376 |
| North boundary: | -10.224 |
| South boundary: | -16.001 |
| Observation types: | chemical, physical |
| Instrument types: | bottle, mass spectrometer |
| Datatypes: | TOXIC METALS |
| Submitter: | |
| Submitting institution: | Biological and Chemical Oceanography Data Management Office |
| Collecting institutions: | The University of Southern Mississippi |
| Contributing projects: | GEOTRACES |
| Platforms: | THOMAS G. THOMPSON (3250) |
| Number of observations: | |
| Supplementary information: | |
| Availability date: | |
| Metadata version: | 1 |
| Keydate: | 2024-04-21 17:24:09+00 |
| Editdate: | 2024-04-21 17:24:52+00 |