Contributors | Affiliation | Role |
---|---|---|
Landry, Michael R. | University of California-San Diego Scripps (UCSD-SIO) | Principal Investigator |
Smith, Walker O. | Virginia Institute of Marine Science (VIMS) | Principal Investigator |
Chandler, Cynthia L. | Woods Hole Oceanographic Institution (WHOI BCO-DMO) | BCO-DMO Data Manager |
Nano and Microplankton Abundances
M.Landry: Nano and microplankton abundances by epifluorescence microscopy W.Smith: Nano and microplankton abundance and carbon biomass
Parameter | Description | Units |
event | event number from event log | |
sta | station number from event log | |
cast | cast number | |
cast_type | CTD = CTD rosette | |
bot | bottle number | |
depth_n | nominal sample depth | meters |
diatom_cen_gt2 | Centric diatoms abundance | cells/liter |
diatom_cen_gt2_C | Centric diatoms biomass | micrograms C/liter |
diatom_pen_gt2 | Pennate diatoms abundance | cells/liter |
diatom_pen_gt2_C | Pennate diatoms biomass | micrograms C/liter |
Phaeo_ant_gt2 | Ph.antarctica colonial cell abundance | cells/liter |
Phaeo_ant_gt2_C | Ph.antarctica colonial cell biomass | micrograms C/liter |
dino_auto_gt2 | Autotrophic dinoflagellate abundance | cells/liter |
dino_auto_gt2_C | Autotrophic dinoflagellate biomass | micrograms C/liter |
dino_het_gt2 | Heterotrophic dinoflagellate abundance | cells/liter |
dino_het_gt2_C | Heterotrophic dinoflagellate biomass | micrograms C/liter |
nanoflag_auto_gt2 | Autotrophic nanoflagellate abundance (excluding dinoflagellates) | cells/liter |
nanoflag_auto_gt2_C | Autotrophic nanoflagellate biomass (excluding dinoflagellates) | micrograms C/liter |
nanoflag_het_gt2 | Heterotrophic nanoflagellate abundance (excluding dinoflagellates) | cells/liter |
nanoflag_het_gt2_C | Heterotrophic nanoflagellate biomass (excluding dinoflagellates) | micrograms C/liter |
mesod_rub_gt2 | Mesodinium rubrum abundance | cells/liter |
mesod_rub_gt2_C | Mesodinium rubrum biomass | micrograms C/liter |
ciliates_n_gt2 | non-loricate ciliate abundance | cells/liter |
ciliates_n_gt2_C | non-loricate ciliate biomass | micrograms C/liter |
olig_mix_gt2 | Plastidic oligotrich abundance including dinoflagellates (Torodinium-like) | cells/liter |
olig_mix_gt2_C | Plastidic oligotrich biomass including dinoflagellates (Torodinium-like) | micrograms C/liter |
tint_gt2 | Tintinnid (loricate ciliate) abundance | cells/liter |
tint_gt2_C | Tintinnid (loricate ciliate) biomass | micrograms C/liter |
hnp_1d5_2 | abundances of heterotrophic nanoplankton, with lengths between 1.5 and 2 um | cells/ml |
hnp_2_5 | abundances of heterotrophic nanoplankton, with lengths between 2 and 5 um | cells/ml |
hnp_5_10 | abundances of heterotrophic nanoplankton, with lengths between 5 and 10 um | cells/ml |
hnp_10_20 | abundances of heterotrophic nanoplankton, with lengths between 10 and 20 um | cells/ml |
hmp | abundances of heterotrophic microplankton, with lengths greater than 20 um | cells/ml |
anp_1d5_2 | abundances of autotrophic nanoplankton, with lengths between 1.5 and 2 um | cells/ml |
anp_2_5 | abundances of autotrophic nanoplankton, with lengths between 2 and 5 um | cells/ml |
anp_5_10 | abundances of autotrophic nanoplankton, with lengths between 5 and 10 um | cells/ml |
anp_10_20 | abundances of autotrophic nanoplankton, with lengths between 10 and 20 um | cells/ml |
amp | abundances of autotrophic microplankton, with lengths greater than 20 um | cells/ml |
diatom | abundance of diatoms | cells/ml |
hnp_C_1d5_2 | biomass of heterotrophic nanoplankton, with lengths between 1.5 and 2 um | ug C/liter |
hnp_C_2_5 | biomass of heterotrophic nanoplankton, with lengths between 2 and 5 um | ug C/liter |
hnp_C_5_10 | biomass of heterotrophic nanoplankton, with lengths between 5 and 10 um | ug C/liter |
hnp_C_10_20 | biomass of heterotrophic nanoplankton, with lengths between 10 and 20 um | ug C/liter |
hmp_C | biomass of heterotrophic microplankton, with lengths greater than 20 um | ug C/liter |
anp_C_1d5_2 | biomass of autotrophic nanoplankton, with lengths between 1.5 and 2 um | ug C/liter |
anp_C_2_5 | biomass of autotrophic nanoplankton, with lengths between 2 and 5 um | ug C/liter |
anp_C_5_10 | biomass of autotrophic nanoplankton, with lengths between 5 and 10 um | ug C/liter |
anp_C_10_20 | biomass of autotrophic nanoplankton, with lengths between 10 and 20 um | ug C/liter |
amp_C | biomass of autotrophic microplankton, with lengths greater than 20 um | ug C/liter |
diatom_C | biomass of diatoms | ug C/liter |
Dataset-specific Instrument Name | Niskin Bottle |
Generic Instrument Name | Niskin bottle |
Dataset-specific Description | CTD clean rosette (Niskin) bottles were used to collect water samples. |
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. |
Dataset-specific Instrument Name | Trace Metal Bottle |
Generic Instrument Name | Trace Metal Bottle |
Dataset-specific Description | Trace metal (TM) clean rosette bottles were used to collect water samples. |
Generic Instrument Description | Trace metal (TM) clean rosette bottle used for collecting trace metal clean seawater samples. |
Website | |
Platform | RVIB Nathaniel B. Palmer |
Report | |
Start Date | 1996-10-02 |
End Date | 1996-11-08 |
Description | Ross Sea Process Study 1 Methods & Sampling PI: Walker O. Smith of: University of Tennessee dataset: Nano and microplankton abundance and carbon biomass dates: October 18, 1996 to November 05, 1996 location: N: -76.4615 S: -78.0348 W: 168.9967 E: -175.9873 project/cruise: AESOPS/NBP96-4A - Ross Sea Process 1 Cruise ship: R/V Nathaniel B. Palmer Methodology Note 1: Although Phaeocystis antarctica colonial cells fall in the nano-size (2-20 micron) phytoplankton, they are part of colonies ranging from 10 to 200 microns. Note 2: Diatoms, dinoflagellates and ciliates range in size from 2-200 microns. Note 3: In the parameter names listed below, gt2 indicates that cells were in the nano-size phytoplankton range, greater than 2 microns. |
Website | |
Platform | RVIB Nathaniel B. Palmer |
Report | |
Start Date | 1997-01-13 |
End Date | 1997-02-11 |
Description | Ross Sea Process Study 2 Methods & Sampling PI: Walker O. Smith of: University of Tennessee dataset: Nano and microplankton abundance and carbon biomass dates: January 13, 1997 to February 08, 1997 location: N: -76.4455 S: -78.043 W: 168.9581 E: -176.0241 project/cruise: AESOPS/NBP97-1 - Ross Sea Process Cruise 2 ship: R/V Nathaniel B. Palmer Methodology Note 1: Although Phaeocystis antarctica colonial cells fall in the nano-size (2-20 micron) phytoplankton, they are part of colonies ranging from 10 to 200 microns. Note 2: Diatoms, dinoflagellates and ciliates range in size from 2-200 microns. Note 3: In the parameter names listed below, gt2 indicates that cells were in the nano-size phytoplankton range, greater than 2 microns. |
Website | |
Platform | R/V Roger Revelle |
Report | |
Start Date | 1997-10-20 |
End Date | 1997-11-24 |
Description | Polar Front Survey I. Additional information about this cruise can be found at https://usjgofs.whoi.edu/aesops/aboutrr6.html Methods & Sampling PI: Michael R. Landry of: University of Hawaii dataset: Nano and microplankton abundances by epifluorescence microscopy dates: October 23, 1997 to November 18, 1997 location: N: -57 S: -62.3658 W: -170.6927 E: -168.2947 project/cruise: AESOPS/KIWI06; APFZ Polar Front Survey 1 cruise ship: R/V Roger A. Revelle Sampling Methodology |
Website | |
Platform | R/V Roger Revelle |
Report | |
Start Date | 1997-12-02 |
End Date | 1998-01-03 |
Description | Polar Front Process I. Additional information about this cruise can be found at https://usjgofs.whoi.edu/aesops/aboutrr7.html Methods & Sampling PI: Michael R. Landry of: University of Hawaii dataset: Nano and microplankton abundances by epifluorescence microscopy dates: December 04, 1997 to December 26, 1997 location: N: -53.0302 S: -64.7418 W: -174.7295 E: -168.8333 project/cruise: AESOPS/KIWI07; APFZ Polar Front Process 1 cruise ship: R/V Roger A. Revelle Sampling Methodology |
Website | |
Platform | R/V Roger Revelle |
Report | |
Start Date | 1998-01-08 |
End Date | 1998-02-08 |
Description | Polar Front Survey II. Additional information about this cruise can be found at https://usjgofs.whoi.edu/aesops/aboutrr8.html Methods & Sampling PI: Michael R. Landry of: University of Hawaii dataset: Nano and microplankton abundances by epifluorescence microscopy dates: January 12, 1998 to January 28, 1998 location: N: -57 S: -67.52 W: -170.1117 E: -169.9983 project/cruise: AESOPS/KIWI08; APFZ Polar Front Survey 2 cruise ship: R/V Roger A. Revelle Sampling Methodology |
Website | |
Platform | R/V Roger Revelle |
Report | |
Start Date | 1998-02-13 |
End Date | 1998-03-19 |
Description | Polar Front Process II. Additional information about this cruise can be found at https://usjgofs.whoi.edu/aesops/aboutrr9.html Methods & Sampling PI: Michael R. Landry of: University of Hawaii dataset: Nano and microplankton abundances by epifluorescence microscopy dates: February 15, 1998 to March 11, 1998 location: N: -52.9678 S: -71.3072 W: -174.7338 E: -165.9145 project/cruise: AESOPS/KIWI09; APFZ Polar Front Process 2 cruise ship: R/V Roger A. Revelle Sampling Methodology |
The U.S. Southern Ocean JGOFS program, called Antarctic Environment and Southern Ocean Process Study (AESOPS), began in August 1996 and continued through March 1998. The U.S. JGOFS AESOPS program focused on two regions in the Southern Ocean: an east/west section of the Ross-Sea continental shelf along 76.5°S, and a second north/south section of the Southern Ocean spanning the Antarctic Circumpolar Current (ACC) at ~170°W (identified as the Polar Front). The science program, coordinated by Antarctic Support Associates (ASA), comprised eleven cruises using the R.V.I.B Nathaniel B. Palmer and R/V Roger Revelle as observational platforms and for deployment and recovery of instrumented moorings and sediment-trap arrays. The Ross-Sea region was occupied on six occasions and the Polar Front five times. Mapping data were obtained from SeaSoar, ADCP, and bathymetric systems. Satellite coverage was provided by the NASA SeaWiFS and the NOAA/NASA Pathfinder programs.
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).