http://lod.bco-dmo.org/id/dataset/2416
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
2009-11-24
ISO 19115-2 Geographic Information - Metadata - Part 2: Extensions for Imagery and Gridded Data
ISO 19115-2:2009(E)
Extracted Chlorophyll and Phaeopigment data collected from R/V Endeavor cruises EN259, EN262, EN264, EN266, and EN267II in the Gulf of Maine and Georges Bank in 1995 as part of the U.S. GLOBEC program (GB project)
2005-08-05
publication
2005-08-05
revision
National Oceanographic Data Center (NODC)
2013-04-04
publication
http://accession.nodc.noaa.gov/0104395
Marine Biological Laboratory/Woods Hole Oceanographic Institution Library (MBLWHOI DLA)
2019-10-28
publication
https://doi.org/10.1575/1912/bco-dmo.2416.1
Dian J. Gifford
University of Rhode Island
principalInvestigator
James P. Manning
Northeast Fisheries Science Center - Woods Hole
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: Gifford, D., Manning, J. (2005) Extracted Chlorophyll and Phaeopigment data collected from R/V Endeavor cruises EN259, EN262, EN264, EN266, and EN267II in the Gulf of Maine and Georges Bank in 1995 as part of the U.S. GLOBEC program (GB project). Biological and Chemical Oceanography Data Management Office (BCO-DMO). (Version 1) Version Date 2005-08-05 [if applicable, indicate subset used]. doi:10.1575/1912/bco-dmo.2416.1 [access date]
Extracted Chlorophyll and Phaeopigment, Georges Bank, 1995. Dataset Description: <h2>Extracted Chlorophyll and Phaeopigment</h2>
<p><strong>DMO note:</strong> The data reported consists of three replicates per each depth horizon sampled.</p>
<p><strong>PI Responsible: Dian J. Gifford</strong></p>
<p>Samples for water column chlorophyll and phaeopigment were collected and analyzed during the following Vital rates 1995 U.S. GLOBEC Georges Bank process cruises:</p>
<p>&nbsp;</p>
<p>&nbsp;</p>
<ul>
<li>EN259</li>
<li>EN262</li>
<li>EN264</li>
<li>EN266</li>
<li>EN267B (aka EN267II and EN267 LEG 2)
<p>Water Collection: Seawater was collected using 10-L teflon-lined Go-flo bottles mounted on the Neil Brown CTD rosette. Water was drained into opaque brown 1-L bottles immediately after collection and refrigerated until processed. Samples were collected onto filters within one hour of water collection. In areas where the water column was well mixed, water was collected from the top, middle and bottom of the water column. When the water column was stratified, water was collected from the top, middles and bottom of the water column as well as around the hydrographic features of interest.</p>
<p>Sample Processing: Samples were prepared for total, &lt;20 µm, and &lt;5 µm chlorophyll and phaeopigment. Samples for total pigments consisted of bulk seawater. Samples for &lt; 20 µm and &lt; 5 µm pigments were passed gently through clean Nitex meshes of appropriate porosity and the filtrate retained for analysis. Three replicate 50-ml samples of each size fraction were collected onto 25 mm GF/F filters, placed into 5 ml of 90% acetone in a capped test tube, and extracted in the freezer for 24 hours prior to analysis.</p>
<p>Sample Analysis: The filters were removed from defrosted test tubes with a clean stainless steel spatula, the tube wiped clean with a Kimwipe, and samples read on a Turner Designs Model 10 fluorometer before and after acidification with 10% HCl (Parsons et al., 1984).</p>
<p>Caveat: In general, pigment concentrations in the &lt;5 µm samples were approximately equal to the &lt;20 µm samples (i.e., there was very little chlorophyll in the 5-20 µm size range: most chlorophyll &lt; 20 µm was also &lt; 5 µm). Because of the difficulty of passing seawater quantitatively through the 5 µm mesh, the &lt;5 µm data are more variable than the Total and &lt; 20 µm data. To avoid confusion, the &lt; 5 µm data are not included in the data files. The data are available, and scientific investigators who need it should contact the PI directly.</p>
<p>Data Use: The data are available for use by any scientific investigator who wishes to use them. The PI must be consulted prior to publication.</p>
<pre>
<strong>Data Submitted by:</strong>
Dian J. Gifford
Graduate School of Oceanography
University of Rhode Island
Narragansett, RI 02882-1197
voice: 401-874-6690
fax: 401-874-6240
e-mail: <a href="mailto:gifford@gsosun1.gso.uri.edu">gifford@gsosun1.gso.uri.edu</a>
<em>updated: Aug 05. 2005, gfh</em>
</pre>
</li>
</ul>
<p>&nbsp;</p>
<p>&nbsp;</p> Methods and Sampling: <p>Seawater was collected using 10-L teflon-lined Go-flo bottles mounted on the Neil Brown CTD rosette. Water was drained into opaque brown 1-L bottles immediately after collection and refrigerated until processed. Samples were collected onto filters within one hour of water collection. In areas where the water column was well mixed, water was collected from the top, middle and bottom of the water column. When the water column was stratified, water was collected from the top, middles and bottom of the water column as well as around the hydrographic features of interest.</p>
Funding provided by National Science Foundation (NSF) Award Number: unknown GB NSF
Funding provided by National Oceanic and Atmospheric Administration (NOAA) Award Number: unknown GB NOAA
completed
Dian J. Gifford
University of Rhode Island
401-874-6690
Narragansett
RI
02882-1197
USA
dgifford@gso.uri.edu
pointOfContact
James P. Manning
Northeast Fisheries Science Center - Woods Hole
508-495-2211
166 Water Street
Woods Hole
MA
02543
USA
james.manning@noaa.gov
pointOfContact
asNeeded
Dataset Version: 1
Unknown
cruiseid
leg
cast
day_local
month_local
year
time_local
lat
lon
depth
chl_a
phaeo
chl_a_20u
phaeo_20u
Go-flo Bottle
theme
None, User defined
cruise id
No BCO-DMO term
cast
day_local
month_local
year
time_local
latitude
longitude
depth
chlorophyll a
total phaeopigment
chl_a_20u
phaeo_20u
featureType
BCO-DMO Standard Parameters
GO-FLO Bottle
instrument
BCO-DMO Standard Instruments
EN259
EN262
EN264
EN266
EN267II
service
Deployment Activity
Gulf of Maine and Georges Bank
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.
U.S. GLOBal ocean ECosystems dynamics
http://www.usglobec.org/
U.S. GLOBal ocean ECosystems dynamics
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).
U.S. GLOBEC
largerWorkCitation
program
U.S. GLOBEC Georges Bank
http://globec.whoi.edu/globec_program.html
U.S. GLOBEC Georges Bank
<p>The U.S. GLOBEC <a href="http://globec.whoi.edu/globec-dir/about_georges_bank.html">Georges Bank</a> Program is a large multi- disciplinary multi-year oceanographic effort. The proximate goal is to understand the population dynamics of key species on the Bank - Cod, <a href="http://globec.whoi.edu/images/haddock103.07.gif">Haddock</a>, and two species of zooplankton (<a href="http://globec.whoi.edu/images/calanus-finmarchicus.html"><em>Calanus finmarchicus</em></a> and <a href="http://globec.whoi.edu/images/pseudocalanus.html"><em>Pseudocalanus</em></a>) - in terms of their coupling to the physical environment and in terms of their <a href="http://globec.whoi.edu/images/targetpp.gif">predators and prey</a>. The ultimate goal is to be able to predict changes in the distribution and abundance of these species as a result of changes in their physical and biotic environment as well as to anticipate how their populations might respond to climate change.</p>
<p>The effort is substantial, requiring broad-scale surveys of the entire Bank, and process studies which focus both on the links between the target species and their physical environment, and the determination of fundamental aspects of these species' life history (birth rates, growth rates, death rates, etc).</p>
<p>Equally important are the modelling efforts that are ongoing which seek to provide realistic predictions of the flow field and which utilize the life history information to produce an integrated view of the dynamics of the populations.</p>
<p>The U.S. GLOBEC Georges Bank <a href="http://globec.whoi.edu/globec-dir/EXCO.html">Executive Committee (EXCO)</a> provides program leadership and effective communication with the funding agencies.</p>
GB
largerWorkCitation
project
eng; USA
oceans
Gulf of Maine and Georges Bank
-68.9588
-65.7268
40.5347
42.3192
1995-01-11
1995-06-16
Georges Bank, Gulf of Maine, Northwest Atlantic Ocean
0
BCO-DMO catalogue of parameters from Extracted Chlorophyll and Phaeopigment data collected from R/V Endeavor cruises EN259, EN262, EN264, EN266, and EN267II in the Gulf of Maine and Georges Bank in 1995 as part of the U.S. GLOBEC program (GB 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/8349.rdf
Name: cruiseid
Units: unknown
Description: <p> Cruise identification</p>
http://lod.bco-dmo.org/id/dataset-parameter/8350.rdf
Name: leg
Units: unknown
Description: <p> Leg of cruise</p>
http://lod.bco-dmo.org/id/dataset-parameter/8351.rdf
Name: cast
Units: dimensionless
Description: <p> Cast number</p>
http://lod.bco-dmo.org/id/dataset-parameter/8352.rdf
Name: day_local
Units: unknown
Description: <p> Day of month, local time</p>
http://lod.bco-dmo.org/id/dataset-parameter/8353.rdf
Name: month_local
Units: unknown
Description: <p> Month of year, local time</p>
http://lod.bco-dmo.org/id/dataset-parameter/8354.rdf
Name: year
Units: unknown
Description: <p> Year</p>
http://lod.bco-dmo.org/id/dataset-parameter/8355.rdf
Name: time_local
Units: HHmm
Description: <p> Local time</p>
http://lod.bco-dmo.org/id/dataset-parameter/8356.rdf
Name: lat
Units: decimal degrees
Description: <p> Latitude</p>
http://lod.bco-dmo.org/id/dataset-parameter/8357.rdf
Name: lon
Units: decimal degrees
Description: <p> Longitude</p>
http://lod.bco-dmo.org/id/dataset-parameter/8358.rdf
Name: depth
Units: meters
Description: <p> Depth of sample</p>
http://lod.bco-dmo.org/id/dataset-parameter/8359.rdf
Name: chl_a
Units: micrograms/liter
Description: <p> Total chlorophyll a</p>
http://lod.bco-dmo.org/id/dataset-parameter/8360.rdf
Name: phaeo
Units: micrograms/liter
Description: <p> Total phaeopigment</p>
http://lod.bco-dmo.org/id/dataset-parameter/8361.rdf
Name: chl_a_20u
Units: micrograms/liter
Description: <p> chlorophyll a pigment, less than 20 micron size fraction </p>
http://lod.bco-dmo.org/id/dataset-parameter/8362.rdf
Name: phaeo_20u
Units: micrograms/liter
Description: <p> phaeopigment, less than 20 micron size fraction </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
37429
https://darchive.mblwhoilibrary.org/bitstream/1912/24716/1/dataset-2416_chlorphaeo__v1.tsv
download
https://doi.org/10.1575/1912/bco-dmo.2416.1
download
onLine
dataset
<p>Seawater was collected using 10-L teflon-lined Go-flo bottles mounted on the Neil Brown CTD rosette. Water was drained into opaque brown 1-L bottles immediately after collection and refrigerated until processed. Samples were collected onto filters within one hour of water collection. In areas where the water column was well mixed, water was collected from the top, middle and bottom of the water column. When the water column was stratified, water was collected from the top, middles and bottom of the water column as well as around the hydrographic features of interest.</p>
from Cruise: EN259 Seawater was collected using 10-L teflon-lined Go-flo bottles mounted on the Neil Brown CTD rosette. Water was drained into opaque brown 1-L bottles immediately after collection and refrigerated until processed. Samples were collected onto filters within one hour of water collection. In areas where the water column was well mixed, water was collected from the top, middle and bottom of the water column. When the water column was stratified, water was collected from the top, middles and bottom of the water column as well as around the hydrographic features of interest.
from Cruise: EN262 Seawater was collected using 10-L teflon-lined Go-flo bottles mounted on the Neil Brown CTD rosette. Water was drained into opaque brown 1-L bottles immediately after collection and refrigerated until processed. Samples were collected onto filters within one hour of water collection. In areas where the water column was well mixed, water was collected from the top, middle and bottom of the water column. When the water column was stratified, water was collected from the top, middles and bottom of the water column as well as around the hydrographic features of interest.
from Cruise: EN264 Seawater was collected using 10-L teflon-lined Go-flo bottles mounted on the Neil Brown CTD rosette. Water was drained into opaque brown 1-L bottles immediately after collection and refrigerated until processed. Samples were collected onto filters within one hour of water collection. In areas where the water column was well mixed, water was collected from the top, middle and bottom of the water column. When the water column was stratified, water was collected from the top, middles and bottom of the water column as well as around the hydrographic features of interest.
from Cruise: EN266 Seawater was collected using 10-L teflon-lined Go-flo bottles mounted on the Neil Brown CTD rosette. Water was drained into opaque brown 1-L bottles immediately after collection and refrigerated until processed. Samples were collected onto filters within one hour of water collection. In areas where the water column was well mixed, water was collected from the top, middle and bottom of the water column. When the water column was stratified, water was collected from the top, middles and bottom of the water column as well as around the hydrographic features of interest.
from Cruise: EN267II Seawater was collected using 10-L teflon-lined Go-flo bottles mounted on the Neil Brown CTD rosette. Water was drained into opaque brown 1-L bottles immediately after collection and refrigerated until processed. Samples were collected onto filters within one hour of water collection. In areas where the water column was well mixed, water was collected from the top, middle and bottom of the water column. When the water column was stratified, water was collected from the top, middles and bottom of the water column as well as around the hydrographic features of interest.
Specified by the Principal Investigator(s)
<p>Sample Processing: Samples were prepared for total, &lt;20 �m, and &lt;5 �m chlorophyll and phaeopigment. Samples for total pigments consisted of bulk seawater. Samples for &lt; 20 �m and &lt; 5 �m pigments were passed gently through clean Nitex meshes of appropriate porosity and the filtrate retained for analysis. Three replicate 50-ml samples of each size fraction were collected onto 25 mm GF/F filters, placed into 5 ml of 90% acetone in a capped test tube, and extracted in the freezer for 24 hours prior to analysis.</p>
<p>Sample Analysis: The filters were removed from defrosted test tubes with a clean stainless steel spatula, the tube wiped clean with a Kimwipe, and samples read on a Turner Designs Model 10 fluorometer before and after acidification with 10% HCl (Parsons et al., 1984).</p>
<p>Caveat: In general, pigment concentrations in the &lt;5 �m samples were approximately equal to the &lt;20 �m samples (i.e., there was very little chlorophyll in the 5-20 �m size range: most chlorophyll &lt; 20 �m was also &lt; 5 �m). Because of the difficulty of passing seawater quantitatively through the 5 �m mesh, the &lt;5 �m data are more variable than the Total and &lt; 20 �m data. To avoid confusion, the &lt; 5 �m data are not included in the data files. The data are available, and scientific investigators who need it should contact the PI directly.</p>
from Cruise: EN259 <p>Sample Processing: Samples were prepared for total, <20 µm,
and <5 µm chlorophyll and phaeopigment. Samples for total
pigments consisted of bulk seawater. Samples for < 20 µm and
< 5 µm pigments were passed gently through clean Nitex meshes of
appropriate porosity and the filtrate retained for analysis. Three
replicate 50-ml samples of each size fraction were collected onto 25
mm GF/F filters, placed into 5 ml of 90% acetone in a capped test
tube, and extracted in the freezer for 24 hours prior to
analysis.</p>
<p>Sample Analysis: The filters were removed from defrosted test
tubes with a clean stainless steel spatula, the tube wiped clean with a Kimwipe, and samples
read on a Turner Designs Model 10 fluorometer before and after
acidification with 10% HCl (Parsons et al., 1984).</p> <p>Caveat:
In general, pigment concentrations in the <5 µm samples were
approximately equal to the <20 µm samples (i.e., there was very
little chlorophyll in the 5-20 µm size range: most chlorophyll <
20 µm was also < 5 µm). Because of the difficulty of passing
seawater quantitatively through the 5 µm mesh, the <5 µm data are
more variable than the Total and < 20 µm data. To avoid
confusion, the < 5 µm data are not included in the data files.
The data are available, and scientific investigators who need it
should contact the PI directly.</p>
from Cruise: EN262 <p>Sample Processing: Samples were prepared for total, <20 µm,
and <5 µm chlorophyll and phaeopigment. Samples for total
pigments consisted of bulk seawater. Samples for < 20 µm and
< 5 µm pigments were passed gently through clean Nitex meshes of
appropriate porosity and the filtrate retained for analysis. Three
replicate 50-ml samples of each size fraction were collected onto 25
mm GF/F filters, placed into 5 ml of 90% acetone in a capped test
tube, and extracted in the freezer for 24 hours prior to
analysis.</p>
<p>Sample Analysis: The filters were removed from defrosted test
tubes with a clean stainless steel spatula, the tube wiped clean with a Kimwipe, and samples
read on a Turner Designs Model 10 fluorometer before and after
acidification with 10% HCl (Parsons et al., 1984).</p> <p>Caveat:
In general, pigment concentrations in the <5 µm samples were
approximately equal to the <20 µm samples (i.e., there was very
little chlorophyll in the 5-20 µm size range: most chlorophyll <
20 µm was also < 5 µm). Because of the difficulty of passing
seawater quantitatively through the 5 µm mesh, the <5 µm data are
more variable than the Total and < 20 µm data. To avoid
confusion, the < 5 µm data are not included in the data files.
The data are available, and scientific investigators who need it
should contact the PI directly.</p>
from Cruise: EN264 <p>Sample Processing: Samples were prepared for total, <20 µm,
and <5 µm chlorophyll and phaeopigment. Samples for total
pigments consisted of bulk seawater. Samples for < 20 µm and
< 5 µm pigments were passed gently through clean Nitex meshes of
appropriate porosity and the filtrate retained for analysis. Three
replicate 50-ml samples of each size fraction were collected onto 25
mm GF/F filters, placed into 5 ml of 90% acetone in a capped test
tube, and extracted in the freezer for 24 hours prior to
analysis.</p>
<p>Sample Analysis: The filters were removed from defrosted test
tubes with a clean stainless steel spatula, the tube wiped clean with a Kimwipe, and samples
read on a Turner Designs Model 10 fluorometer before and after
acidification with 10% HCl (Parsons et al., 1984).</p> <p>Caveat:
In general, pigment concentrations in the <5 µm samples were
approximately equal to the <20 µm samples (i.e., there was very
little chlorophyll in the 5-20 µm size range: most chlorophyll <
20 µm was also < 5 µm). Because of the difficulty of passing
seawater quantitatively through the 5 µm mesh, the <5 µm data are
more variable than the Total and < 20 µm data. To avoid
confusion, the < 5 µm data are not included in the data files.
The data are available, and scientific investigators who need it
should contact the PI directly.</p>
from Cruise: EN266 <p>Sample Processing: Samples were prepared for total, <20 µm,
and <5 µm chlorophyll and phaeopigment. Samples for total
pigments consisted of bulk seawater. Samples for < 20 µm and
< 5 µm pigments were passed gently through clean Nitex meshes of
appropriate porosity and the filtrate retained for analysis. Three
replicate 50-ml samples of each size fraction were collected onto 25
mm GF/F filters, placed into 5 ml of 90% acetone in a capped test
tube, and extracted in the freezer for 24 hours prior to
analysis.</p>
<p>Sample Analysis: The filters were removed from defrosted test
tubes with a clean stainless steel spatula, the tube wiped clean with a Kimwipe, and samples
read on a Turner Designs Model 10 fluorometer before and after
acidification with 10% HCl (Parsons et al., 1984).</p> <p>Caveat:
In general, pigment concentrations in the <5 µm samples were
approximately equal to the <20 µm samples (i.e., there was very
little chlorophyll in the 5-20 µm size range: most chlorophyll <
20 µm was also < 5 µm). Because of the difficulty of passing
seawater quantitatively through the 5 µm mesh, the <5 µm data are
more variable than the Total and < 20 µm data. To avoid
confusion, the < 5 µm data are not included in the data files.
The data are available, and scientific investigators who need it
should contact the PI directly.</p>
from Cruise: EN267II <p>Sample Processing: Samples were prepared for total, <20 µm,
and <5 µm chlorophyll and phaeopigment. Samples for total
pigments consisted of bulk seawater. Samples for < 20 µm and
< 5 µm pigments were passed gently through clean Nitex meshes of
appropriate porosity and the filtrate retained for analysis. Three
replicate 50-ml samples of each size fraction were collected onto 25
mm GF/F filters, placed into 5 ml of 90% acetone in a capped test
tube, and extracted in the freezer for 24 hours prior to
analysis.</p>
<p>Sample Analysis: The filters were removed from defrosted test
tubes with a clean stainless steel spatula, the tube wiped clean with a Kimwipe, and samples
read on a Turner Designs Model 10 fluorometer before and after
acidification with 10% HCl (Parsons et al., 1984).</p> <p>Caveat:
In general, pigment concentrations in the <5 µm samples were
approximately equal to the <20 µm samples (i.e., there was very
little chlorophyll in the 5-20 µm size range: most chlorophyll <
20 µm was also < 5 µm). Because of the difficulty of passing
seawater quantitatively through the 5 µm mesh, the <5 µm data are
more variable than the Total and < 20 µm data. To avoid
confusion, the < 5 µm data are not included in the data files.
The data are available, and scientific investigators who need it
should contact the PI directly.</p>
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
Go-flo Bottle
Go-flo Bottle
PI Supplied Instrument Name: Go-flo Bottle PI Supplied Instrument Description:Seawater was collected using 10-L teflon-lined Go-flo bottles mounted on the Neil Brown CTD rosette. Instrument Name: GO-FLO Bottle Instrument Short Name:GO-FLO Instrument Description: GO-FLO bottle cast used to collect water samples for pigment, nutrient, plankton, etc. The GO-FLO sampling bottle is specially designed to avoid sample contamination at the surface, internal spring contamination, loss of sample on deck (internal seals), and exchange of water from different depths. Community Standard Description: http://vocab.nerc.ac.uk/collection/L05/current/30/
Cruise: EN259
EN259
R/V Endeavor
Community Standard Description
International Council for the Exploration of the Sea
R/V Endeavor
vessel
EN259
Dr Edward Durbin
University of Rhode Island
http://globec.whoi.edu/globec-dir/reports/en259.html
Report describing EN259
Cruise: EN262
EN262
R/V Endeavor
Community Standard Description
International Council for the Exploration of the Sea
R/V Endeavor
vessel
EN262
Cabell S. Davis
Woods Hole Oceanographic Institution
http://globec.whoi.edu/globec-dir/reports/en262/EN262.pdf
Report describing EN262
Cruise: EN264
EN264
R/V Endeavor
Community Standard Description
International Council for the Exploration of the Sea
R/V Endeavor
vessel
EN264
Scott Gallager
Woods Hole Oceanographic Institution
http://globec.whoi.edu/globec-dir/reports/en264.html
Report describing EN264
Cruise: EN266
EN266
R/V Endeavor
Community Standard Description
International Council for the Exploration of the Sea
R/V Endeavor
vessel
EN266
Dian J. Gifford
University of Rhode Island
http://globec.whoi.edu/globec-dir/reports/en266/EN266.pdf
Report describing EN266
Cruise: EN267II
EN267II
R/V Endeavor
Community Standard Description
International Council for the Exploration of the Sea
R/V Endeavor
vessel
EN267II
Cabell S. Davis
Woods Hole Oceanographic Institution
http://globec.whoi.edu/globec-dir/reports/en267L2/EN267L2.pdf
Report describing EN267II
R/V Endeavor
Community Standard Description
International Council for the Exploration of the Sea
R/V Endeavor
vessel