Contributors | Affiliation | Role |
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Ducklow, Hugh W. | Marine Biological Laboratory Ecosystems Center (MBL - Ecosystems) | Principal Investigator |
Sieracki, Michael E. | Virginia Institute of Marine Science (VIMS) | Principal Investigator |
Stoecker, Diane | Woods Hole Oceanographic Institution (WHOI) | Principal Investigator |
Verity, Peter | Skidaway Institute of Oceanography (SkIO) | Principal Investigator |
Chandler, Cynthia L. | Woods Hole Oceanographic Institution (WHOI BCO-DMO) | BCO-DMO Data Manager |
Hugh Ducklow - Bacteria production and abundance
Michael Sieracki - Cyanobacteria, phototrophic, heterotrophic nanoplankton
Diane Stoecker - Ciliates, tintinnids, copepods
Peter Verity - Heterotrophic dinoflagellates
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biology.csv (Comma Separated Values (.csv), 56.23 KB) MD5:91717eb6ac57d637b17fce54eedfc5d8 Primary data file for dataset ID 2600 |
Parameter | Description | Units |
year | year as YYYY | dimensionless |
event | event number from event log | dimensionless |
sta | station number from event log | dimensionless |
cast | cast number | dimensionless |
bot | bottle number | dimensionless |
press | pressure | decibars |
ciliates_pl_o | abundance plastidic oligotrich ciliates, submitted by Stoecker | cells/liter |
ciliates_pl_o_C | biomass of plastidic oligotrich ciliates, submitted by Stoecker | nanograms C/liter |
ciliates_npo | abundance of non plastidic oligotrich ciliates, submitted by Stoecker | cells/liter |
ciliates_npo_C | biomass of non plastidic oligotrich ciliates, submitted by Stoecker | nanograms C/liter |
tint | abundance of tintinnids, Stoecker | cells/liter |
tint_C | biomass of tintinnids, Stoecker, | micrograms C/liter |
mesodin | abundance of Mesodinium, Stoecker | cells/liter |
mesodin_C | biomass of Mesodinium, Stoecker | nanograms C/liter |
ciliates_oth_oli | abundance of other oligotrich ciliates, submitted by Stoecker | cells/liter |
ciliates_oth_oli_C | biomass of other oligotrich ciliates, submitted by Stoecker | nanograms C/liter |
ciliates_oth_no | abundance of other non oligotrich ciliates, submitted by stoecher | cells/liter |
ciliates_oth_no_C | biomass of other non oligotrich ciliates, submitted by Stoecker | nanograms C/liter |
copepod_na | abundance of copepod nauplii, Stoecker | cells/liter |
copepod_oth | abundance of other copepods, Stoecker | cells/liter |
foram | abundance of Foraminifer, | Stoecker |
sticho | abundance of Sticholonche, Stoecker | cells/liter |
holotricha | abundance of Holotricha, | Stoecker |
dino_het | abundance of heterotrophic dinoflagellates submitted by Stoecker | cells/liter |
dino_het_C | biomass of heterotrophic dinoflagellates submitted by Stoecker | micrograms C/liter |
dino_het_lt20 | abundance of heterotrophic dinoflagellates, lt 20 microns, submitted by Verity | cells/milliliter |
dino_het_lt20_biov | mean biovolume of heterotrophic dinoflagellates, lt 20 microns, Verity | microns/milliliter |
dino_het_biov_sd | mean biovolume standard deviation of heterotrophic dinoflagellates, lt 20 microns, submitted by Verity | |
hnp_num | number of cells counted and measured of heterotrophic nanoplankton, Sieracki | |
hnp | abundance of heterotrophic nanoplankton, submitted by Sieracki | cells/milliliter |
hnp_cellv | average cell biovolume heterotrophic nanoplankton, submitted by Sieracki | cubic microns/cell |
hnp_biov | biovolume per sample volume of heterotrophic nanoplankton, submitted by Sieracki | microns/milliliter |
hnp_C | biomass of heterotrophic nanoplankton, submitted by Sieracki | micrograms C/liter |
pnp_num | number of cells counted & measured of phototrophic nanoplankton, Sieracki | |
pnp | abundance of phototrophic nanoplankton, submitted by Sieracki | cells/milliliter |
pnp_cellv | average cell biovolume phototrophic nanoplankton, submitted by Sieracki | cubic microns/cell |
pnp_biov | biovolume per sample volume of phototrophic nanoplankton, submitted by Sieracki | microns/milliliter |
pnp_C | biomass of phototrophic nanoplankton, submitted by Sieracki | micrograms C/liter |
bact_cyan_num | number of cells counted & measured of cyanobacteria, submitted by Sieracki | |
bact_cyan | abundance of cyanobacteria, Sieracki | cells/milliliter |
bact_cyan_cellv | average cell biovolume cyanobacteria, submitted by Sieracki | cubic microns/cell |
bact_cyan_biov | biovolume per sample volume of cyanobacteria, submitted by Sieracki | microns/milliliter |
bact_cyan_C | biomass of cyanobacteria, Sieracki | micrograms C/liter |
thy_incorp | thymidine incorporation, Ducklow | picomoles/liter/hour |
leuc_incorp | leucine incorporation, Ducklow | picomoles/liter/hour |
bact_het_mic | heterotrophic bacteria abundance, microscopy, Ducklow | cells/milliliter |
Dataset-specific Instrument Name | Niskin Bottle |
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 | R/V Atlantis II |
Start Date | 1989-04-17 |
End Date | 1989-05-11 |
Description | early bloom cruise; 17 locations; 60N 21W to 46N 18W Methods & Sampling PI: 1) Hugh Ducklow 2)Michael Sieracki 3)Diane Stoecker 4)Peter Verity of: 1) Horn Point Environmental Laboratory 2) Virginia Institute of Marine Science 3) Woods Hole Oceanographic Institute 4) Skidaway Institute of Oceanography dataset: Merged biological measurements from above Investigators dates: April 20, 1989 to June 06, 1989 location: N: 59.7418 S: 46.25 W: -20.81 E: -17.6433 project/cruise: North Atlantic Bloom Experiment/Atlantis II 119, leg 4 ship: R/V Atlantis II Methodology Bacteria (Ducklow) Additional sampling and analytical methodology (Ducklow) Microplankton (Sieracki, Stoecker, Verity) Protozoa (Stoecker) PI-Notes For Michael Sieracki's measurements: ug C/l = biomass, calculated as um3/ml*F where F is a biovolume to carbon conversion factor. F=200 fgC/um3 DMO note: The Data Management Office has changed the units of the parameters "tint_C" from nanograms to micrograms C/liter and "bact_het_mic" from cells/liter*10^9 to cells/milliliter. All organism counts reported by Diane Stoecker were for organisms greater than 20 microns. |
Website | |
Platform | R/V Atlantis II |
Start Date | 1989-05-15 |
End Date | 1989-06-06 |
Description | late bloom cruise; 31 locations; 61N 22W to 41N 17W Methods & Sampling PI: 1) Hugh Ducklow 2)Michael Sieracki 3)Diane Stoecker 4)Peter Verity of: 1) Horn Point Environmental Laboratory 2) Virginia Institute of Marine Science 3) Woods Hole Oceanographic Institute 4) Skidaway Institute of Oceanography dataset: Merged biological measurements from above Investigators dates: April 20, 1989 to June 06, 1989 location: N: 59.7418 S: 46.25 W: -20.81 E: -17.6433 project/cruise: North Atlantic Bloom Experiment/Atlantis II 119, leg 4 ship: R/V Atlantis II Methodology Bacteria (Ducklow) Additional sampling and analytical methodology (Ducklow) Microplankton (Sieracki, Stoecker, Verity) Protozoa (Stoecker) PI-Notes For Michael Sieracki's measurements: ug C/l = biomass, calculated as um3/ml*F where F is a biovolume to carbon conversion factor. F=200 fgC/um3 DMO note: The Data Management Office has changed the units of the parameters "tint_C" from nanograms to micrograms C/liter and "bact_het_mic" from cells/liter*10^9 to cells/milliliter. All organism counts reported by Diane Stoecker were for organisms greater than 20 microns. |
One of the first major activities of JGOFS was a multinational pilot project, North Atlantic Bloom Experiment (NABE), carried out along longitude 20° West in 1989 through 1991. The United States participated in 1989 only, with the April deployment of two sediment trap arrays at 48° and 34° North. Three process-oriented cruises where conducted, April through July 1989, from R/V Atlantis II and R/V Endeavor focusing on sites at 46° and 59° North. Coordination of the NABE process-study cruises was supported by NSF-OCE award # 8814229. Ancillary sea surface mapping and AXBT profiling data were collected from NASA's P3 aircraft for a series of one day flights, April through June 1989.
A detailed description of NABE and the initial synthesis of the complete program data collection efforts appear in: Topical Studies in Oceanography, JGOFS: The North Atlantic Bloom Experiment (1993), Deep-Sea Research II, Volume 40 No. 1/2.
The U.S. JGOFS Data management office compiled a preliminary NABE data report of U.S. activities: Slagle, R. and G. Heimerdinger, 1991. U.S. Joint Global Ocean Flux Study, North Atlantic Bloom Experiment, Process Study Data Report P-1, April-July 1989. NODC/U.S. JGOFS Data Management Office, Woods Hole Oceanographic Institution, 315 pp. (out of print).
The United States Joint Global Ocean Flux Study was a national component of international JGOFS and an integral part of global climate change research.
The U.S. launched the Joint Global Ocean Flux Study (JGOFS) in the late 1980s to study the ocean carbon cycle. An ambitious goal was set to understand the controls on the concentrations and fluxes of carbon and associated nutrients in the ocean. A new field of ocean biogeochemistry emerged with an emphasis on quality measurements of carbon system parameters and interdisciplinary field studies of the biological, chemical and physical process which control the ocean carbon cycle. As we studied ocean biogeochemistry, we learned that our simple views of carbon uptake and transport were severely limited, and a new "wave" of ocean science was born. U.S. JGOFS has been supported primarily by the U.S. National Science Foundation in collaboration with the National Oceanic and Atmospheric Administration, the National Aeronautics and Space Administration, the Department of Energy and the Office of Naval Research. U.S. JGOFS, ended in 2005 with the conclusion of the Synthesis and Modeling Project (SMP).
Funding Source | Award |
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National Science Foundation (NSF) |