http://lod.bco-dmo.org/id/dataset/2964
eng; USA
utf8
dataset
Highest level of data collection, from a common set of sensors or instrumentation, usually within the same research project
Biological and Chemical Oceanography Data Management Office (BCO-DMO)
Unavailable
508-289-2009
WHOI MS#36
Woods Hole
MA
02543
USA
info@bco-dmo.org
http://www.bco-dmo.org
Monday - Friday 8:00am - 5:00pm
For questions regarding this resource, please contact BCO-DMO via the email address provided.
pointOfContact
2010-06-16
ISO 19115-2 Geographic Information - Metadata - Part 2: Extensions for Imagery and Gridded Data
ISO 19115-2:2009(E)
Bacterial abundance and production from bottle samples from R/V Melville cruise COOK19MV from the Southern Ocean, south of New Zealand in 2002 (SOFeX project)
2008-08-15
publication
2008-08-15
revision
BCO-DMO Linked Data URI
2008-08-15
creation
http://lod.bco-dmo.org/id/dataset/2964
Jacques L. Oliver
Virginia Institute of Marine Science
principalInvestigator
Biological and Chemical Oceanography Data Management Office (BCO-DMO)
Unavailable
508-289-2009
WHOI MS#36
Woods Hole
MA
02543
USA
info@bco-dmo.org
http://www.bco-dmo.org
Monday - Friday 8:00am - 5:00pm
For questions regarding this resource, please contact BCO-DMO via the email address provided.
publisher
Cite this dataset as: Oliver, J. L. (2008) Bacterial abundance and production from bottle samples from R/V Melville cruise COOK19MV from the Southern Ocean, south of New Zealand in 2002 (SOFeX project). Biological and Chemical Oceanography Data Management Office (BCO-DMO). (Version 15 August 2008) Version Date 2008-08-15 [if applicable, indicate subset used]. http://lod.bco-dmo.org/id/dataset/2964 [access date]
Bacterial Abundance and Production from bottle samples Methods and Sampling: <pre>
<b>dates:</b> 24 January 2002 to 21 February 2002 (20020124-20020221)
<b>location:</b> N: -52.56100 S: -66.61150 W: -172.69267 E: -166.94733
</pre>
<br><br>
<p class="text">
15 August 2008: Prepared for OCB data system by Cyndy Chandler, OCB DMO (WHOI) from documentation contributed by Jacques Olivier, Helen Quinby, Robert Daniels, and Hugh Ducklow<br>
</p>
<p><strong>Original Excel file contributed: 8 November, 2002 <br>
and downloaded from MBARI by OCB DMO:</strong>
<a href="http://ocb.whoi.edu/SOFeX/PI-NOTES/data_orig/SOFeX_melville_Bacterial_Data.xls" title="orig file">copy of original Excel file</a></p>
<p><strong>Contact:</strong> Jacques Oliver (Email: jloliver@vims.edu)</p>
<p><strong>R/V Melville Bacterial Measurements Methodology</strong><br>
<br>
<strong>Bacterial Abundance Flow cytometry (FCM) </strong></p>
<p> 1. 9.5 ml sample from CTD or TM rosette, fixed to final concentration of 1% formaldehyde <br>
2. Sample frozen at -80 C <br>
3. On land, triplicate samples were analyzed using a Beckman-Coulter Epics Altra equipped with an Enterprise II laser at 488 nm using 190mV (intra-sample variation). <br>
4. About 100 ml of sample were measured following Troussellier et al. (1999) with addition of 2.5 mM SYTO 13 and a 10 minute incubation. <br>
5. This analysis was done on triplicate 1.0 ml samples to which 1.0 mm beads (Molecular Probes, Fluo Spheres, F-8888) were also added at a 10E6/ml concentration. <br> <br>
The beads determined flow rate and uniformity in fluorescence signal. Discrimination was done on a positive green fluorescence and the plot was green fluorescence (devoid of any red fluorescence) against side scatter. Analytical variation was 3%.
</p>
<p><strong>Reference:</strong> Troussellier, M., C. Courties, P. Lebaron, and P.Servais. 1999. FEMS Microbiology Ecology 29: 319-330.</p>
<br>
<p><strong>Bacterial Abundance Acridine orange direct counts (AODC)</strong>
<pre> 1. 10-15 ml sample fixed to final concentration of 1% formaldehyde
2. Sample filtered onto 0.2 micron blackened polycarbonate filter
3. Filter stained with 45% (w/v) acridine orange
4. Filter mounted onto glass slide with immersion oil and coverslip
5. Bacteria enumerated via epifluorescence microscopy
6. Intra-sample variation reported
</pre>
<br>
<p><strong>Reference:</strong> Kirchman, D., Sigda, J., Kapuscinski, R., and Mitchell, R. 1982. Appl. Envrion. Microbiol. 44:376-382 </p>
<br>
<p><strong>Bacterial Production Thymidine (TdR) and Leucine (Leu) Incorporation</strong>
<pre> 1. 1.6 ml sample spiked with tritiated thymidine or tritiated leucine
2. Samples run in triplicate with one negative control containing 6% trichloroacetic acid (TCA)
3. Samples incubated at in situ temperatures in the dark for 8-20 hours (depending on water temp)
4. Incubation stopped by adding TCA (6% final conc.) to each sample
5. Nucleic acid extracted with TCA and ethanol
6. 1.6 ml Ultima Gold scintillation cocktail added
7. 3 minute counts on each sample on scintillation counter </pre>
<br>
<p><strong>Reference:</strong> Smith, D.C. and Azam, F. 1992. Mar. Microb. Food Webs. 6:107-114.</p>
</pre>
</p>
completed
Jacques L. Oliver
Virginia Institute of Marine Science
VA
jloliver@vims.edu
pointOfContact
asNeeded
Dataset Version: 15 August 2008
Unknown
event
date_L
day_S
lon
lat
patch_loc
station
ev_type
bot
depth
light_lev
bact_cyt
bact_aodc
thy_incorp
thy_sd
leuc_incorp
leuc_sd
Niskin Bottle
Trace Metal Bottle
theme
None, User defined
event
No BCO-DMO term
longitude
latitude
station
bottle number
depth
thymidine incorporation rate
standard deviation of thymidine incorporation rate
leucine incorporation rate
standard deviation of leucine incorporation rate
featureType
BCO-DMO Standard Parameters
Niskin bottle
Trace Metal Bottle
instrument
BCO-DMO Standard Instruments
COOK19MV
service
Deployment Activity
Southern Ocean
place
Locations
otherRestrictions
otherRestrictions
Access Constraints: none. Use Constraints: Please follow guidelines at: http://www.bco-dmo.org/terms-use Distribution liability: Under no circumstances shall BCO-DMO be liable for any direct, incidental, special, consequential, indirect, or punitive damages that result from the use of, or the inability to use, the materials in this data submission. If you are dissatisfied with any materials in this data submission your sole and exclusive remedy is to discontinue use.
Ocean Carbon and Biogeochemistry
http://us-ocb.org/
Ocean Carbon and Biogeochemistry
The Ocean Carbon and Biogeochemistry (OCB) program focuses on the ocean's role as a component of the global Earth system, bringing together research in geochemistry, ocean physics, and ecology that inform on and advance our understanding of ocean biogeochemistry. The overall program goals are to promote, plan, and coordinate collaborative, multidisciplinary research opportunities within the U.S. research community and with international partners. Important OCB-related activities currently include: the Ocean Carbon and Climate Change (OCCC) and the North American Carbon Program (NACP); U.S. contributions to IMBER, SOLAS, CARBOOCEAN; and numerous U.S. single-investigator and medium-size research projects funded by U.S. federal agencies including NASA, NOAA, and NSF.
The scientific mission of OCB is to study the evolving role of the ocean in the global carbon cycle, in the face of environmental variability and change through studies of marine biogeochemical cycles and associated ecosystems.
The overarching OCB science themes include improved understanding and prediction of: 1) oceanic uptake and release of atmospheric CO2 and other greenhouse gases and 2) environmental sensitivities of biogeochemical cycles, marine ecosystems, and interactions between the two.
The OCB Research Priorities (updated January 2012) include: ocean acidification; terrestrial/coastal carbon fluxes and exchanges; climate sensitivities of and change in ecosystem structure and associated impacts on biogeochemical cycles; mesopelagic ecological and biogeochemical interactions; benthic-pelagic feedbacks on biogeochemical cycles; ocean carbon uptake and storage; and expanding low-oxygen conditions in the coastal and open oceans.
OCB
largerWorkCitation
program
Iron Synthesis
https://osprey.bco-dmo.org/program/2017
Iron Synthesis
The two main objectives of the Iron Synthesis program (SCOR Working Group proposal, 2005), are:
1. Data compilation: assembling a common open-access database of the in situ iron experiments, beginning with the first period (1993-2002; Ironex-1, Ironex-2, SOIREE, EisenEx, SEEDS-1; SOFeX, SERIES) where primary articles have already been published, to be followed by the 2004 experiments where primary articles are now in progress (EIFEX, SEEDS-2; SAGE, FeeP); similarly for the natural fertilizations S.O.JGOFS (1992), CROZEX (2004/2005) and KEOPS (2005).
2. Modeling and data synthesis of specific aspects of two or more such experiments for various topics such as physical mixing, phytoplankton productivity, overall ecosystem functioning, iron chemistry, CO2 budgeting, nutrient uptake ratios, DMS(P) processes, and combinations of these variables and processes.
SCOR Working Group proposal, 2005. "The Legacy of in situ Iron Enrichments: Data Compilation and Modeling".
http://www.scor-int.org/Working_Groups/wg131.htm
See also: SCOR Proceedings Vol. 42 Concepcion, Chile October 2006, pgs: 13-16 2.3.3 Working Group on The Legacy of in situ Iron Enrichments: Data Compilation and Modeling.
The first objective of the Iron Synthesis program involves a data recovery effort aimed at assembling a common, open-access database of data and metadata from a series of in-situ ocean iron fertilization experiments conducted between 1993 and 2005. Initially, funding for this effort is being provided by the Scientific Committee on Oceanic Research (SCOR) and the U.S. National Science Foundation (NSF).
Through the combined efforts of the principal investigators of the individual projects and the staff of Biological and Chemical Oceanography Data Management Office (BCO-DMO), data currently available primarily through individuals, disparate reports and data agencies, and in multiple formats, are being collected and prepared for addition to the BCO-DMO database from which they will be freely available to the community.
As data are contributed to the BCO-DMO office, they are organized into four overlapping categories:
1. Level 1, basic metadata
(e.g., description of project/study, general location, PI(s), participants);
2. Level 2, detailed metadata and basic shipboard data and routine ship's operations
(e.g., CTDs, underway measurements, sampling event logs);
3. Level 3, detailed metadata and data from specialized observations
(e.g., discrete observations, experimental results, rate measurements) and
4. Level 4, remaining datasets
(e.g., highest level of detailed data available from each study).
Collaboration with BCO-DMO staff began in March of 2008 and initial efforts have been directed toward basic project descriptions, levels 1 and 2 metadata and basic data, with detailed and more detailed data files being incorporated as they become available and are processed.
Related file
Program Documentation
The Iron Synthesis Program is funded jointly by the Scientific Committee on Oceanic Research (SCOR) and the U.S. National Science Foundation (NSF).
FeSynth
largerWorkCitation
program
Southern Ocean Iron Experiment
http://www.mbari.org/expeditions/SOFeX2002/
Southern Ocean Iron Experiment
<p>Before he passed away in 1993, John Martin suggested that an increase in the flow of iron-rich dust to the ocean causes phytoplankton (single celled algae) to grow. The increased photosynthesis removes carbon dioxide from surface waters as the algae create biomass. This carbon dioxide is replaced by carbon dioxide gas that flows into the sea from the atmosphere. Reduced carbon dioxide in the atmosphere cools the planet (CO2 is a greenhouse gas that warms the earth). The results of this work, funded by the National Science Foundation, the Department of Energy, and the US Coast Guard, will be a much better understanding of how biological processes may regulate climate. (see Related Info: Fe cycle)</p>
<p>A direct test of the 'Martin Hypothesis' that trace concentrations of Fe are responsible for phytoplankton's ability to grow by direct experimental addition of Fe to the surface waters. Consequently the distribution of bioavailable Fe in the surface waters determines large geographical areas primary production and the following flux of fixed organic matter to the deep sea. The aim of the SOFeX project is to investigate the effects of iron fertilization on the productivity of the Southern Ocean. The results of this work will contribute significantly to our understanding of important biogeochemical processes which bear directly on the global carbon cycle, atmospheric carbon dioxide concentration, and climate control.</p>
<p>The SOFeX-N and SOFeX-S designations are sometimes used to distinguish between two iron enriched patches - one in low silicate waters north of the polar front (SOFEX-N), and the other in high silicate waters south of the polar front (SOFEX-S). All three ships, Melville (MV), Revelle (RR) and Polar Star (PS), worked in SOFEX-S, but only the Revelle and Melville worked in the SOFeX N patch and shuttled between the two patches.</p>
SOFeX
largerWorkCitation
project
eng; USA
oceans
Southern Ocean
2008-08-15
Southern Ocean, south of New Zealand
0
BCO-DMO catalogue of parameters from Bacterial abundance and production from bottle samples from R/V Melville cruise COOK19MV from the Southern Ocean, south of New Zealand in 2002 (SOFeX project)
Biological and Chemical Oceanography Data Management Office (BCO-DMO)
Unavailable
508-289-2009
WHOI MS#36
Woods Hole
MA
02543
USA
info@bco-dmo.org
http://www.bco-dmo.org
Monday - Friday 8:00am - 5:00pm
For questions regarding this resource, please contact BCO-DMO via the email address provided.
pointOfContact
http://lod.bco-dmo.org/id/dataset-parameter/14965.rdf
Name: event
Units: doYhhmm
Description: <p>unique sampling event number from event log (day of year and time (UTC))</p>
http://lod.bco-dmo.org/id/dataset-parameter/14966.rdf
Name: date_L
Units: dimensionless
Description: <p>NZ local day</p>
http://lod.bco-dmo.org/id/dataset-parameter/14967.rdf
Name: day_S
Units: integer days
Description: <p>South patch local date days since start of first fertilization, day zero=24-Jan ??</p>
http://lod.bco-dmo.org/id/dataset-parameter/14968.rdf
Name: lon
Units: decimal degrees
Description: <p>longitude; negative denotes West</p>
http://lod.bco-dmo.org/id/dataset-parameter/14969.rdf
Name: lat
Units: decimal degrees
Description: <p>latitude; negative denotes South</p>
http://lod.bco-dmo.org/id/dataset-parameter/14970.rdf
Name: patch_loc
Units: dimensionless
Description: <p>sampling location relative to patch see explanation in cruise event log), T = transect</p>
http://lod.bco-dmo.org/id/dataset-parameter/14971.rdf
Name: station
Units: dimensionless
Description: <p>station location number</p>
http://lod.bco-dmo.org/id/dataset-parameter/14972.rdf
Name: ev_type
Units: dimensionless
Description: <p>event type descriptor string</p>
http://lod.bco-dmo.org/id/dataset-parameter/14973.rdf
Name: bot
Units: dimensionless
Description: <p>Niskin bottle number</p>
http://lod.bco-dmo.org/id/dataset-parameter/14974.rdf
Name: depth
Units: meters
Description: <p>depth, calculted from pressure??</p>
http://lod.bco-dmo.org/id/dataset-parameter/14975.rdf
Name: light_lev
Units: percent
Description: <p>light level</p>
http://lod.bco-dmo.org/id/dataset-parameter/14976.rdf
Name: bact_cyt
Units: cells/liter
Description: <p>bacterial abundance, Flow Cytometry (FCM)</p>
http://lod.bco-dmo.org/id/dataset-parameter/14977.rdf
Name: bact_aodc
Units: cells/liter
Description: <p>bacterial abundance, Acridine Orange Direct Count (AODC)</p>
http://lod.bco-dmo.org/id/dataset-parameter/14978.rdf
Name: thy_incorp
Units: picomoles/liter/hour
Description: <p>Thymidine (TdR) incorporation rate</p>
http://lod.bco-dmo.org/id/dataset-parameter/14979.rdf
Name: thy_sd
Units: picomoles/liter/hour
Description: <p>standard deviation of thymidine incorporation rate</p>
http://lod.bco-dmo.org/id/dataset-parameter/14980.rdf
Name: leuc_incorp
Units: picomoles/liter/hour
Description: <p>Leucine incorporation rate</p>
http://lod.bco-dmo.org/id/dataset-parameter/14981.rdf
Name: leuc_sd
Units: picomoles/liter/hour
Description: <p>standard deviation of leucine incorporation rate</p>
GB/NERC/BODC > British Oceanographic Data Centre, Natural Environment Research Council, United Kingdom
Biological and Chemical Oceanography Data Management Office (BCO-DMO)
Unavailable
508-289-2009
WHOI MS#36
Woods Hole
MA
02543
USA
info@bco-dmo.org
http://www.bco-dmo.org
Monday - Friday 8:00am - 5:00pm
For questions regarding this resource, please contact BCO-DMO via the email address provided.
pointOfContact
15154
https://datadocs.bco-dmo.org/file/B11vMZjsJ1NvA/bacteria.csv
bacteria.csv
Primary data file for dataset ID 2964
download
https://osprey.bco-dmo.org/dataset/2964/data/download
download
onLine
dataset
<pre>
<b>dates:</b> 24 January 2002 to 21 February 2002 (20020124-20020221)
<b>location:</b> N: -52.56100 S: -66.61150 W: -172.69267 E: -166.94733
</pre>
<br><br>
<p class="text">
15 August 2008: Prepared for OCB data system by Cyndy Chandler, OCB DMO (WHOI) from documentation contributed by Jacques Olivier, Helen Quinby, Robert Daniels, and Hugh Ducklow<br>
</p>
<p><strong>Original Excel file contributed: 8 November, 2002 <br>
and downloaded from MBARI by OCB DMO:</strong>
<a href="http://ocb.whoi.edu/SOFeX/PI-NOTES/data_orig/SOFeX_melville_Bacterial_Data.xls" title="orig file">copy of original Excel file</a></p>
<p><strong>Contact:</strong> Jacques Oliver (Email: jloliver@vims.edu)</p>
<p><strong>R/V Melville Bacterial Measurements Methodology</strong><br>
<br>
<strong>Bacterial Abundance Flow cytometry (FCM) </strong></p>
<p> 1. 9.5 ml sample from CTD or TM rosette, fixed to final concentration of 1% formaldehyde <br>
2. Sample frozen at -80 C <br>
3. On land, triplicate samples were analyzed using a Beckman-Coulter Epics Altra equipped with an Enterprise II laser at 488 nm using 190mV (intra-sample variation). <br>
4. About 100 ml of sample were measured following Troussellier et al. (1999) with addition of 2.5 mM SYTO 13 and a 10 minute incubation. <br>
5. This analysis was done on triplicate 1.0 ml samples to which 1.0 mm beads (Molecular Probes, Fluo Spheres, F-8888) were also added at a 10E6/ml concentration. <br> <br>
The beads determined flow rate and uniformity in fluorescence signal. Discrimination was done on a positive green fluorescence and the plot was green fluorescence (devoid of any red fluorescence) against side scatter. Analytical variation was 3%.
</p>
<p><strong>Reference:</strong> Troussellier, M., C. Courties, P. Lebaron, and P.Servais. 1999. FEMS Microbiology Ecology 29: 319-330.</p>
<br>
<p><strong>Bacterial Abundance Acridine orange direct counts (AODC)</strong>
<pre> 1. 10-15 ml sample fixed to final concentration of 1% formaldehyde
2. Sample filtered onto 0.2 micron blackened polycarbonate filter
3. Filter stained with 45% (w/v) acridine orange
4. Filter mounted onto glass slide with immersion oil and coverslip
5. Bacteria enumerated via epifluorescence microscopy
6. Intra-sample variation reported
</pre>
<br>
<p><strong>Reference:</strong> Kirchman, D., Sigda, J., Kapuscinski, R., and Mitchell, R. 1982. Appl. Envrion. Microbiol. 44:376-382 </p>
<br>
<p><strong>Bacterial Production Thymidine (TdR) and Leucine (Leu) Incorporation</strong>
<pre> 1. 1.6 ml sample spiked with tritiated thymidine or tritiated leucine
2. Samples run in triplicate with one negative control containing 6% trichloroacetic acid (TCA)
3. Samples incubated at in situ temperatures in the dark for 8-20 hours (depending on water temp)
4. Incubation stopped by adding TCA (6% final conc.) to each sample
5. Nucleic acid extracted with TCA and ethanol
6. 1.6 ml Ultima Gold scintillation cocktail added
7. 3 minute counts on each sample on scintillation counter </pre>
<br>
<p><strong>Reference:</strong> Smith, D.C. and Azam, F. 1992. Mar. Microb. Food Webs. 6:107-114.</p>
</pre>
</p>
from Cruise: COOK19MV <pre>
<b>dates:</b> 24 January 2002 to 21 February 2002 (20020124-20020221)
<b>location:</b> N: -52.56100 S: -66.61150 W: -172.69267 E: -166.94733
</pre>
<br><br>
<p class="text">
15 August 2008: Prepared for OCB data system by Cyndy Chandler, OCB DMO (WHOI) from documentation contributed by Jacques Olivier, Helen Quinby, Robert Daniels, and Hugh Ducklow<br>
</p>
<p><strong>Original Excel file contributed: 8 November, 2002 <br>
and downloaded from MBARI by OCB DMO:</strong>
<a href="http://ocb.whoi.edu/SOFeX/PI-NOTES/data_orig/SOFeX_melville_Bacterial_Data.xls" title="orig file">copy of original Excel file</a></p>
<p><strong>Contact:</strong> Jacques Oliver (Email: jloliver@vims.edu)</p>
<p><strong>R/V Melville Bacterial Measurements Methodology</strong><br>
<br>
<strong>Bacterial Abundance Flow cytometry (FCM) </strong></p>
<p> 1. 9.5 ml sample from CTD or TM rosette, fixed to final concentration of 1% formaldehyde <br>
2. Sample frozen at -80 C <br>
3. On land, triplicate samples were analyzed using a Beckman-Coulter Epics Altra equipped with an Enterprise II laser at 488 nm using 190mV (intra-sample variation). <br>
4. About 100 ml of sample were measured following Troussellier et al. (1999) with addition of 2.5 mM SYTO 13 and a 10 minute incubation. <br>
5. This analysis was done on triplicate 1.0 ml samples to which 1.0 mm beads (Molecular Probes, Fluo Spheres, F-8888) were also added at a 10E6/ml concentration. <br> <br>
The beads determined flow rate and uniformity in fluorescence signal. Discrimination was done on a positive green fluorescence and the plot was green fluorescence (devoid of any red fluorescence) against side scatter. Analytical variation was 3%.
</p>
<p><strong>Reference:</strong> Troussellier, M., C. Courties, P. Lebaron, and P.Servais. 1999. FEMS Microbiology Ecology 29: 319-330.</p>
<br>
<p><strong>Bacterial Abundance Acridine orange direct counts (AODC)</strong>
<pre> 1. 10-15 ml sample fixed to final concentration of 1% formaldehyde
2. Sample filtered onto 0.2 micron blackened polycarbonate filter
3. Filter stained with 45% (w/v) acridine orange
4. Filter mounted onto glass slide with immersion oil and coverslip
5. Bacteria enumerated via epifluorescence microscopy
6. Intra-sample variation reported
</pre>
<br>
<p><strong>Reference:</strong> Kirchman, D., Sigda, J., Kapuscinski, R., and Mitchell, R. 1982. Appl. Envrion. Microbiol. 44:376-382 </p>
<br>
<p><strong>Bacterial Production Thymidine (TdR) and Leucine (Leu) Incorporation</strong>
<pre> 1. 1.6 ml sample spiked with tritiated thymidine or tritiated leucine
2. Samples run in triplicate with one negative control containing 6% trichloroacetic acid (TCA)
3. Samples incubated at in situ temperatures in the dark for 8-20 hours (depending on water temp)
4. Incubation stopped by adding TCA (6% final conc.) to each sample
5. Nucleic acid extracted with TCA and ethanol
6. 1.6 ml Ultima Gold scintillation cocktail added
7. 3 minute counts on each sample on scintillation counter </pre>
<br>
<p><strong>Reference:</strong> Smith, D.C. and Azam, F. 1992. Mar. Microb. Food Webs. 6:107-114.</p>
</pre>
</p>
Specified by the Principal Investigator(s)
<pre>
Change history:
070509: downloaded original data (SOFeX_melville_Bacterial_Data.xls) from SOFeX project data web site.
data prepared database by Dave DuBois (OCB DMO, WHOI)
080815: added to OCB database by Cyndy Chandler, OCB DMO, (cchandler@whoi.edu)
OCB DMO Note: Four worksheets were contained in the original file: Methods, North Patch,
South Patch, and Transects. The Methods worksheet was extracted to file
Methods_Melville_Bact_Abund_Prod.xls. The other three worksheets were combined into one
and were sorted by date. The Latitude value for Transect 3, Station 42 was changed from
6 07.06 S to 66 07.06 S before converting all Lat and Lon values to decimal degrees.
Two bottle cast entries were included for USCG Polar Star on 16-Feb in the original file
and are retained here with data collected during the Melville cruise.
PI note: Date = Local Day (Kiwi). Event # = Julian Day, UTC.
North Patch Summary: 2 IN, 2 OUT.
South Patch Summary: 7 IN, 4 OUT (R/V Melville); 1 IN, 1 OUT (USCG Polar Star).
Transect Summary: 3 transects.
</pre>
from Cruise: COOK19MV <pre>
Change history:
070509: downloaded original data (SOFeX_melville_Bacterial_Data.xls) from SOFeX project data web site.
data prepared database by Dave DuBois (OCB DMO, WHOI)
080815: added to OCB database by Cyndy Chandler, OCB DMO, (cchandler@whoi.edu)
OCB DMO Note: Four worksheets were contained in the original file: Methods, North Patch,
South Patch, and Transects. The Methods worksheet was extracted to file
Methods_Melville_Bact_Abund_Prod.xls. The other three worksheets were combined into one
and were sorted by date. The Latitude value for Transect 3, Station 42 was changed from
6 07.06 S to 66 07.06 S before converting all Lat and Lon values to decimal degrees.
Two bottle cast entries were included for USCG Polar Star on 16-Feb in the original file
and are retained here with data collected during the Melville cruise.
PI note: Date = Local Day (Kiwi). Event # = Julian Day, UTC.
North Patch Summary: 2 IN, 2 OUT.
South Patch Summary: 7 IN, 4 OUT (R/V Melville); 1 IN, 1 OUT (USCG Polar Star).
Transect Summary: 3 transects.
</pre>
Specified by the Principal Investigator(s)
asNeeded
7.x-1.1
Biological and Chemical Oceanography Data Management Office (BCO-DMO)
Unavailable
508-289-2009
WHOI MS#36
Woods Hole
MA
02543
USA
info@bco-dmo.org
http://www.bco-dmo.org
Monday - Friday 8:00am - 5:00pm
For questions regarding this resource, please contact BCO-DMO via the email address provided.
pointOfContact
Niskin Bottle
Niskin Bottle
PI Supplied Instrument Name: Niskin Bottle Instrument Name: Niskin bottle Instrument Short Name:Niskin bottle 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. Community Standard Description: http://vocab.nerc.ac.uk/collection/L22/current/TOOL0412/
Trace Metal Bottle
Trace Metal Bottle
PI Supplied Instrument Name: Trace Metal Bottle Instrument Name: Trace Metal Bottle Instrument Short Name:TM Bottle Instrument Description: Trace metal (TM) clean rosette bottle used for collecting trace metal clean seawater samples. Community Standard Description: http://vocab.nerc.ac.uk/collection/L05/current/30/
Cruise: COOK19MV
COOK19MV
R/V Melville
Community Standard Description
International Council for the Exploration of the Sea
R/V Melville
vessel
COOK19MV
Kenneth H. Coale
Moss Landing Marine Laboratories
http://ocb.whoi.edu/SOFeX/CRUISES/proj_description.pdf
Report describing COOK19MV
R/V Melville
Community Standard Description
International Council for the Exploration of the Sea
R/V Melville
vessel