Nano and Microplankton Abundances from RVIB Nathaniel B. Palmer, R/V Roger Revelle NBP-96-4A, NBP-97-1, KIWI6, KIWI7, KIWI8, KIWI9 cruises in the Southern Ocean, 1997-1998 (U.S. JGOFS AESOPS project)

Website: https://www.bco-dmo.org/dataset/2744
Version: final
Version Date: 2002-03-13

Project
» U.S. JGOFS Antarctic Environment and Southern Ocean Process Study (AESOPS)

Program
» U.S. Joint Global Ocean Flux Study (U.S. JGOFS)
ContributorsAffiliationRole
Landry, Michael R.University of California-San Diego (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


Dataset Description

Nano and Microplankton Abundances


Methods & Sampling

M.Landry: Nano and microplankton abundances by epifluorescence microscopy

W.Smith: Nano and microplankton abundance and carbon biomass
 

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Parameters

ParameterDescriptionUnits
eventevent number from event log
stastation number from event log
castcast number
cast_typeCTD = CTD rosette TM = trace metal rosette
botbottle number
depth_nnominal sample depth meters
diatom_cen_gt2Centric diatoms abundance cells/liter
diatom_cen_gt2_CCentric diatoms biomass micrograms C/liter
diatom_pen_gt2Pennate diatoms abundance cells/liter
diatom_pen_gt2_CPennate diatoms biomass micrograms C/liter
Phaeo_ant_gt2Ph.antarctica colonial cell abundance cells/liter
Phaeo_ant_gt2_CPh.antarctica colonial cell biomass micrograms C/liter
dino_auto_gt2Autotrophic dinoflagellate abundance cells/liter
dino_auto_gt2_CAutotrophic dinoflagellate biomass micrograms C/liter
dino_het_gt2Heterotrophic dinoflagellate abundance cells/liter
dino_het_gt2_CHeterotrophic dinoflagellate biomass micrograms C/liter
nanoflag_auto_gt2Autotrophic nanoflagellate abundance (excluding dinoflagellates) cells/liter
nanoflag_auto_gt2_CAutotrophic nanoflagellate biomass (excluding dinoflagellates) micrograms C/liter
nanoflag_het_gt2Heterotrophic nanoflagellate abundance (excluding dinoflagellates) cells/liter
nanoflag_het_gt2_CHeterotrophic nanoflagellate biomass (excluding dinoflagellates) micrograms C/liter
mesod_rub_gt2Mesodinium rubrum abundance cells/liter
mesod_rub_gt2_CMesodinium rubrum biomass micrograms C/liter
ciliates_n_gt2non-loricate ciliate abundance cells/liter
ciliates_n_gt2_Cnon-loricate ciliate biomass micrograms C/liter
olig_mix_gt2Plastidic oligotrich abundance including dinoflagellates (Torodinium-like) cells/liter
olig_mix_gt2_CPlastidic oligotrich biomass including dinoflagellates (Torodinium-like) micrograms C/liter
tint_gt2Tintinnid (loricate ciliate) abundance cells/liter
tint_gt2_CTintinnid (loricate ciliate) biomass micrograms C/liter
hnp_1d5_2abundances of heterotrophic nanoplankton, with lengths between 1.5 and 2 um cells/ml
hnp_2_5abundances of heterotrophic nanoplankton, with lengths between 2 and 5 um cells/ml
hnp_5_10abundances of heterotrophic nanoplankton, with lengths between 5 and 10 um cells/ml
hnp_10_20abundances of heterotrophic nanoplankton, with lengths between 10 and 20 um cells/ml
hmpabundances of heterotrophic microplankton, with lengths greater than 20 um cells/ml
anp_1d5_2abundances of autotrophic nanoplankton, with lengths between 1.5 and 2 um cells/ml
anp_2_5abundances of autotrophic nanoplankton, with lengths between 2 and 5 um cells/ml
anp_5_10abundances of autotrophic nanoplankton, with lengths between 5 and 10 um cells/ml
anp_10_20abundances of autotrophic nanoplankton, with lengths between 10 and 20 um cells/ml
ampabundances of autotrophic microplankton, with lengths greater than 20 um cells/ml
diatomabundance of diatoms cells/ml
hnp_C_1d5_2biomass of heterotrophic nanoplankton, with lengths between 1.5 and 2 um ug C/liter
hnp_C_2_5biomass of heterotrophic nanoplankton, with lengths between 2 and 5 um ug C/liter
hnp_C_5_10biomass of heterotrophic nanoplankton, with lengths between 5 and 10 um ug C/liter
hnp_C_10_20biomass of heterotrophic nanoplankton, with lengths between 10 and 20 um ug C/liter
hmp_Cbiomass of heterotrophic microplankton, with lengths greater than 20 um ug C/liter
anp_C_1d5_2biomass of autotrophic nanoplankton, with lengths between 1.5 and 2 um ug C/liter
anp_C_2_5biomass of autotrophic nanoplankton, with lengths between 2 and 5 um ug C/liter
anp_C_5_10biomass of autotrophic nanoplankton, with lengths between 5 and 10 um ug C/liter
anp_C_10_20biomass of autotrophic nanoplankton, with lengths between 10 and 20 um ug C/liter
amp_Cbiomass of autotrophic microplankton, with lengths greater than 20 um ug C/liter
diatom_Cbiomass of diatoms ug C/liter


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Instruments

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.


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Deployments

NBP-96-04A

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.

NBP-97-01

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.

KIWI6

Website
Platform
R/V Roger Revelle
Report
Start Date
1997-10-20
End Date
1997-11-24
Description
Polar Front Survey I

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

KIWI7

Website
Platform
R/V Roger Revelle
Report
Start Date
1997-12-02
End Date
1998-01-03
Description
Polar Front Process I

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

KIWI8

Website
Platform
R/V Roger Revelle
Report
Start Date
1998-01-08
End Date
1998-02-08
Description
Polar Front Survey II

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

KIWI9

Website
Platform
R/V Roger Revelle
Report
Start Date
1998-02-13
End Date
1998-03-19
Description
Polar Front Process II

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


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Project Information

U.S. JGOFS Antarctic Environment and Southern Ocean Process Study (AESOPS)


Coverage: Southern Ocean, Ross Sea


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.



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Program Information

U.S. Joint Global Ocean Flux Study (U.S. JGOFS)


Coverage: Global


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).



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