| Contributors | Affiliation | Role |
|---|---|---|
| Hashim, Mohammed | Woods Hole Oceanographic Institution (WHOI) | Principal Investigator |
| Conte, Maureen H. | Bermuda Institute of Ocean Sciences (BIOS) | Co-Principal Investigator |
| Pedrosa Pàmies, Rut | Marine Biological Laboratory (MBL) | Co-Principal Investigator |
| Subhas, Adam V. | Woods Hole Oceanographic Institution (WHOI) | Co-Principal Investigator |
| Bish, David | Indiana University | Scientist |
| Crowley, Stephen F. | University of Liverpool | Scientist |
| Dennis, Paul F. | University of East Anglia (UEA) | Scientist |
| Perry, Chris T. | University of Exeter | Scientist |
| Salter, Michael A. | University of Exeter | Scientist |
| Wilson, Rod W. | University of Exeter | Scientist |
| Hayden, Matthew G. | Woods Hole Oceanographic Institution (WHOI) | Technician |
| Weber, J.C. | Marine Biological Laboratory (MBL) | Technician |
| Rauch, Shannon | Woods Hole Oceanographic Institution (WHOI BCO-DMO) | BCO-DMO Data Manager |
Samples were either measured or compiled in the literature (references are provided in the dataset). Newly measured data were collected using either an IRMS or a Picarro. All sample analyses were calibrated with respect to VPDB via contiguous measurement of local secondary laboratory reference materials.
- Imported original file "Stable isotope data.xlsx" into the BCO-DMO system.
- Flagged "N/A" and "NA" as missing data identifiers (missing data are blank/empty in the final CSV file).
- Made west longitude values negative.
- Renamed fields to comply with BCO-DMO naming conventions.
- Changed spelling from "Staiger" to "Steiger" in the "Source" column.
- Saved the final file as "960397_v1_ofp_carbo_and_oxygen_isotopes.csv".
| File |
|---|
960397_v1_ofp_carbo_and_oxygen_isotopes.csv (Comma Separated Values (.csv), 48.21 KB) MD5:d484c13cf06c4b9d35295f3cb624206c Primary data file for dataset ID 960397, version 1 |
| Parameter | Description | Units |
| Sample_ID_or_Common_name | The ID of the analyzed sample. Note: the sample ID of the individual foraminifera and pteropod data from OFP traps at 3200 m depth was not specified in the studies of Deuser and Ross (1989), Deuser et al. (1982), Fabry and Deuser (1992), and Deuser and Jasper (1993). | unitless |
| Species | Species of the sample if applicable (in case of a biogenic sample) | unitless |
| Sample_type | The type of sample | unitless |
| Latitude | Latitude of sample collection | decimal degrees |
| Longitude | Longitude of sample collection | decimal degrees |
| Diet | Description of diet, if applicable (normal diet or sardine fed) | unitless |
| d13C | Carbon isotope of carbonate (inorganic) | per mil with respect to VPDB |
| d13C_stdev | The standard deviation of carbon isotopes | per mil with respect to VPDB |
| d18O | Oxygen isotope of carbonate (inorganic) | per mil with respect to VPDB |
| O18_stdev | The standard deviation of oxygen isotopes | per mil with respect to VPDB |
| Source | Source of the sample. See Related Publications section of metadata for full citations. | unitless |
| Dataset-specific Instrument Name | Picarro is G-2131i |
| Generic Instrument Name | Gas Analyzer |
| Generic Instrument Description | Gas Analyzers - Instruments for determining the qualitative and quantitative composition of gas mixtures. |
| Dataset-specific Instrument Name | IRMS |
| Generic Instrument Name | Isotope-ratio Mass Spectrometer |
| Generic 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). |
| Website | |
| Platform | OFP_mooring |
| Start Date | 1978-04-06 |
| Description | The Oceanic Flux Program (OFP) time-series began in 1978 at the Hydrostation S hydrographic time-series site (32 05N, 64 15W), located approximately 45 km southeast of Bermuda. The time-series was originally called the SCIFF (Seasonal Changes in Isotopes and Flux of Foraminifera) program.
Location:
1978-1984: 31deg 10min N, 64deg 30min W, 3300m (SCIFF site)
1984-2010: 31deg 50min N, 64deg 10min W, 4500m
2011-present: 31deg 55 N, 64deg 05 W, 4550m |
NSF Award Abstract:
OCE-PRF Towards Quantifying Calcium Carbonate Sediment Dissolution During Marine Diagenesis The goal of the project is to investigate dissolution of calcium carbonate (CaCO3) in sediments below the seafloor and determine its importance to the chemistry of seawater. This project uses sediment samples and chemical data collected from different parts of the ocean during the past five decades by scientific ocean drilling programs. Sediment dissolution of carbonate can lessen the impact of ocean acidification, the process that causes the pH of the ocean to decrease due to the uptake of carbon dioxide (CO2) from the atmosphere. Ocean acidification threatens the survival of marine organisms, such as oysters, clams, and coral reefs, which could alter marine food chains and food supply to humans. By improving understanding of carbonate dissolution in the ocean, results from this project will enable better predictions of the effects of ocean acidification on marine organisms. This will advance the progress of science and contribute to the knowledge that can inform public policy. In addition, understanding carbonate sediment dissolution serves other important purposes. For example, dissolution can create small spaces between sediments that may get filled with groundwater once sediments convert to rocks over millions of years. Thus, understanding the occurrence and spatial distribution of spaces within rocks may help determine the volume and movement of groundwater in subsurface aquifers. This project provides support for a postdoctoral research fellow and research training opportunities for students through the Summer Student Fellowship and Woods Hole-wide Partnership Education Programs at the Woods Hole Oceanographic Institution.
Carbonate mineral dissolution is an integral part of the alkalinity and carbon cycles in the ocean and is expected to play an increasingly significant role in mediating changes in ocean chemistry as atmospheric CO2 continues to rise. The goal of this project is to provide thermodynamic constraints necessary for quantifying carbonate sediment dissolution in marine diagenetic environments. Specifically, the CaCO3 saturation state of pore fluids will be calculated in 365 globally distributed sites from previous scientific ocean drilling expeditions using a specially developed Pitzer ion activity model which is particularly useful for calculating activity coefficients in high ionic strength solutions such as those that characterize most diagenetic environments. These calculations will be substantiated with geochemical and textural analyses of sediment samples from four representative sites to identify the specific diagenetic processes (e.g., dissolution, precipitation, and recrystallization) and document the conditions responsible for their occurrence and prevalence. The immediate advantage of calculating the saturation state of pore fluids is that such data can be used to estimate carbonate sediment dissolution below the seafloor and quantify its contribution to the alkalinity and carbon cycles, which will lead to more accurate predictions of the consequences of ocean acidification. Another benefit of the global saturation state dataset is that it will improve our understanding of authigenic carbonate precipitation and its link to the carbon cycle over Earth history, which has been proposed as a significant sink for carbon. Furthermore, by complementing the thermodynamic calculations with textural and geochemical analyses, this project will parse out various diagenetic processes and identify the sedimentological and geochemical conditions responsible for their occurrence. Such knowledge is crucial for evaluating the impact of diagenesis on the carbonate-hosted paleoenvironmental proxies. Collectively, this project will pave the way towards a mechanistic understanding of carbonate diagenesis. This will provide important constraints on the oceanic alkalinity cycle, carbon burial rates, and geochemical proxies, which ultimately help us better understand the future of our ocean system in the context of climate change.
This award reflects NSF's statutory mission and has been deemed worthy of support through evaluation using the Foundation's intellectual merit and broader impacts review criteria.
| Funding Source | Award |
|---|---|
| NSF Division of Ocean Sciences (NSF OCE) |