Contributors | Affiliation | Role |
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Goldstein, Steven L. | Lamont-Doherty Earth Observatory (LDEO) | Principal Investigator |
Pena, Leopoldo D. | University of Barcelona (U Barcelona) | Co-Principal Investigator |
Wu, Yingzhe | Lamont-Doherty Earth Observatory (LDEO) | Student, Contact |
Bolge, Louise L. | Lamont-Doherty Earth Observatory (LDEO) | Technician |
Copley, Nancy | Woods Hole Oceanographic Institution (WHOI BCO-DMO) | BCO-DMO Data Manager |
Seawater samples were collected in the GEOTRACES GA02 Cruise Leg 3 from Punta Arenas (Chile) to Las Palmas (Spain), March-April 2011. 5-10 L of seawater were collected depending on the sample depth and stored in a cubitainer for each sample. The samples were filtered using 0.2 μm Sartobran cartridges and acidified using ultrapure Seastar hydrochloric acid (HCl) to pH ~ 2 shortly after sampling.
We preconcentrated rare earth elements from seawater using C18 cartridges (Waters Corp., Sep-Pak classic C18 cartridge 360 mg 55-105 μm) loaded with complexing agent of 2-ethylhexyl hydrogen phosphate (HDEHP) and 2-ethylhexyl dihydrogen phosphate (H2MEHP), which was first proposed by Shabani et al. (1992). In this study, we followed the method by Jeandel et al. (1998), Lacan and Jeandel (2004), Pahnke et al. (2012). Specifically, C18 cartridges were first cleaned in a 0.5N HCl bath overnight, then 10 mL of 6N HCl were introduced through the cartridge, and then they were flushed with > 500 mL of Milli-Q water. Cartridges were in a neutral environment (MilliQ® water) after cleaning. For each 5 L sample, 300 μL of complexing agent HDEHP/H2MEHP was loaded on a clean cartridge. Seawater samples were adjusted to pH ~ 3.5 by adding Optima® ammonium hydroxide. The seawater samples were pumped through the cartridges at 20mL/min by a peristaltic pump. Afterward, the cartridges were eluted with 10 mL of 0.01N HCl to remove barium. After barium elution, the cartridges were eluted with 35 mL of 6N hydrochloric acid at 10 mL/min by the peristaltic pump to collect the REEs. The REEs were dried and further purified by Eichrom RE-spec column chemistry. Nd fractions were extracted from REEs by LN-spec column chemistry.
The Nd isotopic ratios were measured on MC-ICP-MS (a ThermoScientific Neptune-Plus®) at Lamont-Doherty Earth Observatory of Columbia University. Nd fractions from column chemistry were dried by evaporation and dissolved in 600-800 μL of 3% nitric acid (HNO3). The international Nd standard JNdi-1 was analyzed between every sample and the average of the standards is reported relative to the recommended value of 143Nd/144Nd = 0.512115 (Tanaka, 2000). For different concentrations of JNdi-1, the measured 143Nd/144Nd isotopic ratios were 0.512079 ± 0.000014 (2σ, n = 126) for 20ppb solutions, 0.512079 ± 0.000013 (2σ, n = 190) for 15 ppb solutions, and 0.512058 ± 0.000022 (2σ, n = 37) for 10ppb solutions. Nd isotopic ratios were normalized to 146Nd/144Nd = 0.7219 for mass fractionation.
We are awaiting the results of Nd isotopic ratios at the crossover station (~40°S and ~42°W) from University of Cambridge.
The Nd isotopic composition is expressed as εNd = [(143Nd/144Ndsample/143Nd/144NdCHUR) - 1] × 104, where 143Nd/144NdCHUR = 0.512638 (Jacobsen and Wasserburg, 1980).
BCO-DMO Processing notes:
- added conventional header with dataset name, PI name, version date
- modified parameter names to conform with BCO-DMO naming conventions
- blank values replaced with no data value 'nd'
- replaced spaces with underscores
- converted BTL_ISO_DateTime_UTC to standard format
- reduced decimals of Nd values
File |
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Nd_diss_GA02.csv (Comma Separated Values (.csv), 48.84 KB) MD5:d127dcb6ff635a73256323d6ca5027a5 Primary data file for dataset ID 672203 |
Parameter | Description | Units |
cruise_id | Cruise name | unitless |
cruise_name | Cruise section | unitless |
station | Station number | unitless |
cast | Cast number | unitless |
cast_type | Cast type | unitless |
instrument | Sampling Device | unitless |
bottle | Bottle number | unitless |
BODC_Bottle | British Oceanographic Data Center Bottle Number | unitless |
depth_CTD | Sampling depth of CTD | meters |
depth_GEOTRC_CTD_round | Sampling depth rounded to nearest meter | meters |
BTL_ISO_DateTime_UTC | UTC date and time of collection formatted as yyyy-mm--ddTHH:MM:SSZ | unitless |
lat_sta | Latitude; north is positive | degrees north |
lon_sta | Longitude; east is positive | degrees east |
press_CTD | Sampling pressure of CTD | dbar |
temp_CTD | Sampling temperature of CTD | degrees Celsius |
sal_CTD | Sampling salinity of CTD | PSU |
O2_CTD | Sampling oxygen concentration of CTD | micromole/kilogram (umol/kg) |
Phosphate | Phosphate concentration | micromole/kilogram (umol/kg) |
Silicate | Silicate concentration | micromole/kilogram (umol/kg) |
Nitrate | Nitrate concentration | micromole/kilogram (umol/kg) |
Nd_143_144_D_Ratio | 143Nd/144Nd isotopic ratio | dimensionless |
Nd_143_144_D_Ratio_Flag | Quality flag: Flag 1: data evaluated as Good; Flag 2: data quality not evaluated or unknown; Flag 3: data quality assessed to be questionable; Flag 4: data quality assessed to be Bad; Flag 9: no data | unitless |
Nd_143_144_D_Ratio_Int_2SE | Internal 2 standard errors of each sample | dimensionless |
Nd_143_144_D_Ratio_Ext_2SD | External 2 standard deviations of repeatedly measured JNdi standards during the analysis | dimensionless |
Nd_D_Epsilon | Final 143Nd/144Nd normalized to 0.512638 in parts per 10000 | dimensionless |
Nd_D_Epsilon_Flag | Quality flag: Flag 1: data evaluated as Good; Flag 2: data quality not evaluated or unknown; Flag 3: data quality assessed to be questionable; Flag 4: data quality assessed to be Bad; Flag 9: no data | unitless |
Nd_D_Epsilon_Int_2SE | Internal 2 standard errors of each sample normalized to 0.512638 in parts per 10000 | dimensionless |
Nd_D_Epsilon_Ext_2SD | External 2 standard deviations of repeatedly measured JNdi standards during the analysis normalized to 0.512638 in parts per 10000 | dimensionless |
Dataset-specific Instrument Name | |
Generic Instrument Name | CTD - profiler |
Generic Instrument Description | The Conductivity, Temperature, Depth (CTD) unit is an integrated instrument package designed to measure the conductivity, temperature, and pressure (depth) of the water column. The instrument is lowered via cable through the water column. It permits scientists to observe the physical properties in real-time via a conducting cable, which is typically connected to a CTD to a deck unit and computer on a ship. The CTD is often configured with additional optional sensors including fluorometers, transmissometers and/or radiometers. It is often combined with a Rosette of water sampling bottles (e.g. Niskin, GO-FLO) for collecting discrete water samples during the cast.
This term applies to profiling CTDs. For fixed CTDs, see https://www.bco-dmo.org/instrument/869934. |
Dataset-specific Instrument Name | MC-ICP-MS (ThermoScientific Neptune-Plus) |
Generic Instrument Name | Inductively Coupled Plasma Mass Spectrometer |
Dataset-specific Description | Measured Nd isotopic ratios |
Generic Instrument Description | An ICP Mass Spec is an instrument that passes nebulized samples into an inductively-coupled gas plasma (8-10000 K) where they are atomized and ionized. Ions of specific mass-to-charge ratios are quantified in a quadrupole mass spectrometer. |
Dataset-specific Instrument Name | |
Generic Instrument Name | Niskin bottle |
Generic Instrument Description | A Niskin bottle (a next generation water sampler based on the Nansen bottle) is a cylindrical, non-metallic water collection device with stoppers at both ends. The bottles can be attached individually on a hydrowire or deployed in 12, 24, or 36 bottle Rosette systems mounted on a frame and combined with a CTD. Niskin bottles are used to collect discrete water samples for a range of measurements including pigments, nutrients, plankton, etc. |
Website | |
Platform | RRS James Cook |
Report | |
Start Date | 2011-02-03 |
End Date | 2011-06-03 |
Extracted from the NSF award abstract:
Neodymium (Nd) isotopes are increasingly used in paleoceanographic studies as "quasi-conservative" water mass tracers. However, the limitations of this proxy are not yet fully understood. The proposed work aims to address this uncertainty by critically evaluating the behavior of Nd isotopes as tracers of water mass mixing. The project, led by researchers at Columbia University's Lamont-Doherty Earth Observatory, will analyze in-hand seawater and surface sediment samples collected along a meridional transect in the southwest Atlantic (0 to 50 degrees S) during a GEOTRACES cruise. The sample suite will be used to test 1) whether Nd isotope ratios deviate from expected values for mixing along circulation transport paths, 2) whether Nd isotopes behave quasi-conservatively away from continental margins, 3) whether seafloor features (e.g., continental shelf, volcanic seamounts) add significant external Nd to the system, and 4) whether the Southern Hemisphere wind zones impact Nd isotope values through aeolian deposition. The relationship between Nd isotopes in authigenic surface sediments and those in the overlying seawater will be calibrated for the first time.
By testing an emerging tool in the study of past ocean dynamics, this research will enable a more accurate understanding of changes in the ocean-climate system. The project will support an early-career researcher and a graduate student. Undergraduate students will be involved through an NSF-supported summer internship program at LDEO.
GEOTRACES is a SCOR sponsored program; and funding for program infrastructure development is provided by the U.S. National Science Foundation.
GEOTRACES gained momentum following a special symposium, S02: Biogeochemical cycling of trace elements and isotopes in the ocean and applications to constrain contemporary marine processes (GEOSECS II), at a 2003 Goldschmidt meeting convened in Japan. The GEOSECS II acronym referred to the Geochemical Ocean Section Studies To determine full water column distributions of selected trace elements and isotopes, including their concentration, chemical speciation, and physical form, along a sufficient number of sections in each ocean basin to establish the principal relationships between these distributions and with more traditional hydrographic parameters;
* To evaluate the sources, sinks, and internal cycling of these species and thereby characterize more completely the physical, chemical and biological processes regulating their distributions, and the sensitivity of these processes to global change; and
* To understand the processes that control the concentrations of geochemical species used for proxies of the past environment, both in the water column and in the substrates that reflect the water column.
GEOTRACES will be global in scope, consisting of ocean sections complemented by regional process studies. Sections and process studies will combine fieldwork, laboratory experiments and modelling. Beyond realizing the scientific objectives identified above, a natural outcome of this work will be to build a community of marine scientists who understand the processes regulating trace element cycles sufficiently well to exploit this knowledge reliably in future interdisciplinary studies.
Expand "Projects" below for information about and data resulting from individual US GEOTRACES research projects.
Funding Source | Award |
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NSF Division of Ocean Sciences (NSF OCE) |