Mean respiration and excretion rates for plankton from ARSV Laurence M. Gould and RVIB Nathaniel B. Palmer cruises LMG0104, LMG0203, NBP0104, and NBP0204 in the Southern Ocean from 2001-2002 (SOGLOBEC project)

Website: https://www.bco-dmo.org/dataset/2371
Data Type: Cruise Results
Version: 1
Version Date: 2002-12-05

Project
» U.S. GLOBEC Southern Ocean (SOGLOBEC)

Program
» U.S. GLOBal ocean ECosystems dynamics (U.S. GLOBEC)
ContributorsAffiliationRole
Torres, Joseph J.University of South Florida (USF)Principal Investigator
Allison, DickyWoods Hole Oceanographic Institution (WHOI BCO-DMO)BCO-DMO Data Manager

Abstract
Mean respiration and excretion rates for plankton from ARSV Laurence M. Gould and RVIB Nathaniel B. Palmer cruises LMG0104, LMG0203, NBP0104, and NBP0204 in the Southern Ocean from 2001-2002 (SOGLOBEC project)


Coverage

Temporal Extent: 2001-01-01 - 2002-12-31

Dataset Description

Mean respiration and excretion rates for plankton Southern Ocean GLOBEC

Contact:
Jose Torres
College of Marine Science
University of South Florida
140 Seventh Avenue, South
St. Petersburg, FL 33701
jtorres@marine.usf.edu


Methods & Sampling

Collection of specimens. Crustaceans were collected using either mouth-closing Tucker trawls (9.0 m2 or 2.25 m2 mouth area) or downward-looking, vertically deployed plummet nets (1 m2 mouth area). Tucker trawls were equipped with either blind or thermal-turbulence-protecting cod-ends (Childress etal. 1978); plummet nets terminated in bind cod-ends only. Specimens were taken in the upper 1000m of the water column in the vicinity of the marginal ice zone during spring (November-December) 1983, fall (March) 1986, and winter (June-August) 1988 as part of the AMERIEZ (Antarctic Marine Ecosystem Research at the Ice Edge Zone) program to study ice edge biology. Sampling locations were all in the Scotia-Weddell Sea region but moved with seasonal movement of the pack ice edge. Thus, spring and winter collections were in the Scotia Sea in the vicinity of 60 °S, 40°W; fall sampling took place further south, 65°S, 46°W. Collections were made on a continuum from deep in the pack ice out to 300 km seaward of the ice edge in fall and winter. In spring, collections were made in the open water only. Station locations are given in Donnelly et al (1990).


Data Processing Description

Oxygen consumption rates were determined by allowing individuals to deplete the oxygen in a sealed container filled with filtered (0.45 um pore size) seawater. Temperature was maintained at 0.5 °C (+/- 0.1 °C) using a refrigerated water bath. Oxygen partial pressure (PO2) was continuously monitored using a Clark polarographic oxygen electrode (Clark 1956) as an individual reduced oxygen levels to low (10 to 20 mm Hg) partial pressures. Electrodes were calibrated using air- and nitrogen-saturated seawater at the experimental temperature. The time required for consumption of oxygen to low levels varied from 12 to 18 h. Streptomycin and Neomycin (each 25 mg 1-1) were added to the seawater to minimize microbial growth. To control for possible oxygen consumption by microorganishs, an individual was removed after selected runs, its volume was replaced with fresh seawater, and oxygen consumption was again measured for 2 to 4 h. In all cases microbial oxygen consumption was negligibly low.


[ table of contents | back to top ]

Data Files

File
mean_rates_plankton_rs.csv
(Comma Separated Values (.csv), 3.67 KB)
MD5:7cf689ae8a3cf3bbf32e4bcfe7b29526
Primary data file for dataset ID 2371

[ table of contents | back to top ]

Parameters

ParameterDescriptionUnits
speciesSpecies name. text
seasonSeason of the year (fall or winter). text
numberNumber of individuals in the calculation of the mean, four cruises represented. integer
stageSize of the animal. unitless
WetMass_mgMean wet mass of individuals in milligrams, four cruises represented. mg
WetMass_stdevStandard deviation of WetMass. mg
H2OMean percent water in animals, four cruises represented. percent
H2O_stdevStandard deviation of H2O. percent
AshMean percent Ash in animal, four cruises represented. percent
Ash_stdevStandard deviation of Ash. percent
O2_consumedMean O2 consumed per individual per hour, four cruises represented. uL O2 per individual per hour
O2_consumed_stdevStandard deviation of O2_consumed. uL O2 per individual per hour
VO2Mean oxygen consumed per mg wet weight per hour, four cruises represented. uL O2 per mg wet weight per hr
VO2_stdevStandard deviation of VO2. uL O2 per mg wet weight per hr
N_excreteMean of micrograms nitrogen excreted per individual per hour, four cruises represented. ug per individual per hour
N_excrete_stdevStandard deviation of N_excrete. ug per individual per hour
N_excrete_massMean of micrograms nitrogen excreted per milligram of wet mass per hour, four cruises represented. ug N per mg wet mass per hour
N_excrete_mass_stdevStandard deviation of N_excrete_mass. ug N per mg wet mass per hour
OtoNmean oxygen to nitrogen ratio, four cruises represented unitless
OtoN_stdevStandard deviation of OtoN. unitless


[ table of contents | back to top ]

Instruments

Dataset-specific Instrument Name
Tucker Trawl
Generic Instrument Name
Tucker Trawl
Dataset-specific Description
Tucker trawls (9.0 m2 or 2.25 m 2 mouth area) were equipped with either blind or thermal-turbulence-protecting cod-nets (Childress etal. 1978)
Generic Instrument Description
The original Tucker Trawl, a net with a rectangular mouth opening first built in 1951 by G.H. Tucker, was not an opening/closing system, but shortly thereafter it was modified so that it could be opened and closed.  The original had a 183 cm by 183 cm flexible rectangular mouth opening 914 cm long net with 1.8 cm stretched mesh for the first 457 cm and 1.3 cm mesh for last 457 cm. 152 cm of coarse plankton or muslin netting lined the end of the net. Tucker designed the net to collect animals associated with the deep scattering layers, principally euphausiids, siphonophores, and midwater fish. (from Wiebe and Benfield, 2003). Currently used Tucker Trawls usually have 1-m2 openings and can have a single net or multiple nets on the frame.


[ table of contents | back to top ]

Deployments

LMG0104

Website
Platform
ARSV Laurence M. Gould
Report
Start Date
2001-04-20
End Date
2001-06-05
Description
Methods & Sampling
Collection of specimens. Crustaceans were collected using either mouth-closing Tucker trawls (9.0 m2 or 2.25 m2 mouth area) or downward-looking, vertically deployed plummet nets (1 m2 mouth area). Tucker trawls were equipped with either blind or thermal-turbulence-protecting cod-ends (Childress etal. 1978); plummet nets terminated in bind cod-ends only. Specimens were taken in the upper 1000m of the water column in the vicinity of the marginal ice zone during spring (November-December) 1983, fall (March) 1986, and winter (June-August) 1988 as part of the AMERIEZ (Antarctic Marine Ecosystem Research at the Ice Edge Zone) program to study ice edge biology. Sampling locations were all in the Scotia-Weddell Sea region but moved with seasonal movement of the pack ice edge. Thus, spring and winter collections were in the Scotia Sea in the vicinity of 60� S, 40� W; fall sampling took place further south, 65� S, 46� W. Collections were made on a continuum from deep in the pack ice out to 300 km seaward of the ice edge in fall and winter. In spring, collections were made in the open water only. Station locations are given in Donnelly etal (1990).

Processing Description
Oxygen consumption rates were determined by allowing individuals to deplete the oxygen in a sealed container filled with filtered (0.45 um pore size) seawater. Temperature was maintained at 0.5�C (�0.1�C) using a refrigerated water bath. Oxygen partial pressure (PO2) was continuously monitored using a Clark polarographic oxygen electrode (Clark 1956) as an individual reduced oxygen levels to low (10 to 20 mm Hg) partial pressures. Electrodes were calibrated using air- and nitrogen-saturated seawater at the experimental temperature. The time required for consumption of oxygen to low levels varied from 12 to 18 h. Streptomycin and Neomycin (each 25 mg 1-1) were added to the seawater to minimize microbial growth. To control for possible oxygen consumption by microorganishs, an individual was removed after selected runs, its volume was replaced with fresh seawater, and oxygen consumption was again measured for 2 to 4 h. In all cases microbial oxygen consumption was negligibly low.

LMG0203

Website
Platform
ARSV Laurence M. Gould
Report
Start Date
2002-04-07
End Date
2002-05-20
Description
Methods & Sampling
Collection of specimens. Crustaceans were collected using either mouth-closing Tucker trawls (9.0 m2 or 2.25 m2 mouth area) or downward-looking, vertically deployed plummet nets (1 m2 mouth area). Tucker trawls were equipped with either blind or thermal-turbulence-protecting cod-ends (Childress etal. 1978); plummet nets terminated in bind cod-ends only. Specimens were taken in the upper 1000m of the water column in the vicinity of the marginal ice zone during spring (November-December) 1983, fall (March) 1986, and winter (June-August) 1988 as part of the AMERIEZ (Antarctic Marine Ecosystem Research at the Ice Edge Zone) program to study ice edge biology. Sampling locations were all in the Scotia-Weddell Sea region but moved with seasonal movement of the pack ice edge. Thus, spring and winter collections were in the Scotia Sea in the vicinity of 60� S, 40� W; fall sampling took place further south, 65� S, 46� W. Collections were made on a continuum from deep in the pack ice out to 300 km seaward of the ice edge in fall and winter. In spring, collections were made in the open water only. Station locations are given in Donnelly etal (1990).

Processing Description
Oxygen consumption rates were determined by allowing individuals to deplete the oxygen in a sealed container filled with filtered (0.45 um pore size) seawater. Temperature was maintained at 0.5�C (�0.1�C) using a refrigerated water bath. Oxygen partial pressure (PO2) was continuously monitored using a Clark polarographic oxygen electrode (Clark 1956) as an individual reduced oxygen levels to low (10 to 20 mm Hg) partial pressures. Electrodes were calibrated using air- and nitrogen-saturated seawater at the experimental temperature. The time required for consumption of oxygen to low levels varied from 12 to 18 h. Streptomycin and Neomycin (each 25 mg 1-1) were added to the seawater to minimize microbial growth. To control for possible oxygen consumption by microorganishs, an individual was removed after selected runs, its volume was replaced with fresh seawater, and oxygen consumption was again measured for 2 to 4 h. In all cases microbial oxygen consumption was negligibly low.

NBP0104

Website
Platform
RVIB Nathaniel B. Palmer
Report
Start Date
2001-07-22
End Date
2001-08-31
Description
Methods & Sampling
Collection of specimens. Crustaceans were collected using either mouth-closing Tucker trawls (9.0 m2 or 2.25 m2 mouth area) or downward-looking, vertically deployed plummet nets (1 m2 mouth area). Tucker trawls were equipped with either blind or thermal-turbulence-protecting cod-ends (Childress etal. 1978); plummet nets terminated in bind cod-ends only. Specimens were taken in the upper 1000m of the water column in the vicinity of the marginal ice zone during spring (November-December) 1983, fall (March) 1986, and winter (June-August) 1988 as part of the AMERIEZ (Antarctic Marine Ecosystem Research at the Ice Edge Zone) program to study ice edge biology. Sampling locations were all in the Scotia-Weddell Sea region but moved with seasonal movement of the pack ice edge. Thus, spring and winter collections were in the Scotia Sea in the vicinity of 60� S, 40� W; fall sampling took place further south, 65� S, 46� W. Collections were made on a continuum from deep in the pack ice out to 300 km seaward of the ice edge in fall and winter. In spring, collections were made in the open water only. Station locations are given in Donnelly etal (1990).

Processing Description
Oxygen consumption rates were determined by allowing individuals to deplete the oxygen in a sealed container filled with filtered (0.45 um pore size) seawater. Temperature was maintained at 0.5�C (�0.1�C) using a refrigerated water bath. Oxygen partial pressure (PO2) was continuously monitored using a Clark polarographic oxygen electrode (Clark 1956) as an individual reduced oxygen levels to low (10 to 20 mm Hg) partial pressures. Electrodes were calibrated using air- and nitrogen-saturated seawater at the experimental temperature. The time required for consumption of oxygen to low levels varied from 12 to 18 h. Streptomycin and Neomycin (each 25 mg 1-1) were added to the seawater to minimize microbial growth. To control for possible oxygen consumption by microorganishs, an individual was removed after selected runs, its volume was replaced with fresh seawater, and oxygen consumption was again measured for 2 to 4 h. In all cases microbial oxygen consumption was negligibly low.

NBP0204

Website
Platform
RVIB Nathaniel B. Palmer
Report
Start Date
2002-07-31
End Date
2002-09-18
Description
Also see NBP0204 Cruise Data Report

Methods & Sampling
Collection of specimens. Crustaceans were collected using either mouth-closing Tucker trawls (9.0 m2 or 2.25 m2 mouth area) or downward-looking, vertically deployed plummet nets (1 m2 mouth area). Tucker trawls were equipped with either blind or thermal-turbulence-protecting cod-ends (Childress etal. 1978); plummet nets terminated in bind cod-ends only. Specimens were taken in the upper 1000m of the water column in the vicinity of the marginal ice zone during spring (November-December) 1983, fall (March) 1986, and winter (June-August) 1988 as part of the AMERIEZ (Antarctic Marine Ecosystem Research at the Ice Edge Zone) program to study ice edge biology. Sampling locations were all in the Scotia-Weddell Sea region but moved with seasonal movement of the pack ice edge. Thus, spring and winter collections were in the Scotia Sea in the vicinity of 60� S, 40� W; fall sampling took place further south, 65� S, 46� W. Collections were made on a continuum from deep in the pack ice out to 300 km seaward of the ice edge in fall and winter. In spring, collections were made in the open water only. Station locations are given in Donnelly etal (1990).

Processing Description
Oxygen consumption rates were determined by allowing individuals to deplete the oxygen in a sealed container filled with filtered (0.45 um pore size) seawater. Temperature was maintained at 0.5�C (�0.1�C) using a refrigerated water bath. Oxygen partial pressure (PO2) was continuously monitored using a Clark polarographic oxygen electrode (Clark 1956) as an individual reduced oxygen levels to low (10 to 20 mm Hg) partial pressures. Electrodes were calibrated using air- and nitrogen-saturated seawater at the experimental temperature. The time required for consumption of oxygen to low levels varied from 12 to 18 h. Streptomycin and Neomycin (each 25 mg 1-1) were added to the seawater to minimize microbial growth. To control for possible oxygen consumption by microorganishs, an individual was removed after selected runs, its volume was replaced with fresh seawater, and oxygen consumption was again measured for 2 to 4 h. In all cases microbial oxygen consumption was negligibly low.


[ table of contents | back to top ]

Project Information

U.S. GLOBEC Southern Ocean (SOGLOBEC)


Coverage: Southern Ocean


The fundamental objectives of United States Global Ocean Ecosystems Dynamics (U.S. GLOBEC) Program are dependent upon the cooperation of scientists from several disciplines. Physicists, biologists, and chemists must make use of data collected during U.S. GLOBEC field programs to further our understanding of the interplay of physics, biology, and chemistry. Our objectives require quantitative analysis of interdisciplinary data sets and, therefore, data must be exchanged between researchers. To extract the full scientific value, data must be made available to the scientific community on a timely basis.



[ table of contents | back to top ]

Program Information

U.S. GLOBal ocean ECosystems dynamics (U.S. GLOBEC)


Coverage: Global


U.S. GLOBEC (GLOBal ocean ECosystems dynamics) is a research program organized by oceanographers and fisheries scientists to address the question of how global climate change may affect the abundance and production of animals in the sea.

The U.S. GLOBEC Program currently had major research efforts underway in the Georges Bank / Northwest Atlantic Region, and the Northeast Pacific (with components in the California Current and in the Coastal Gulf of Alaska). U.S. GLOBEC was a major contributor to International GLOBEC efforts in the Southern Ocean and Western Antarctic Peninsula (WAP).



[ table of contents | back to top ]

Funding

Funding SourceAward
NSF Antarctic Sciences (NSF ANT)

[ table of contents | back to top ]