Chlorophyll-a on F/V Sea Eagle and F/V Frosti salmon trawl cruises in the Northeast Pacific in 2000 as part of the U.S. GLOBEC program (NEP project)

Website: https://www.bco-dmo.org/dataset/2463
Data Type: Cruise Results
Version: 1
Version Date: 2007-04-11

Project
» U.S. GLOBEC Northeast Pacific (NEP)

Program
» U.S. GLOBal ocean ECosystems dynamics (U.S. GLOBEC)
ContributorsAffiliationRole
Brodeur, Richard DNational Oceanic and Atmospheric Administration (NOAA)Co-Principal Investigator
Pool, Suzan SOregon State University (OSU-CIMRS)Co-Principal Investigator
Allison, DickyWoods Hole Oceanographic Institution (WHOI BCO-DMO)BCO-DMO Data Manager

Abstract
Chlorophyll-a on F/V Sea Eagle and F/V Frosti salmon trawl cruises in the Northeast Pacific in 2000 as part of the U.S. GLOBEC program (NEP project)


Coverage

Spatial Extent: N:44.7043 E:-124.1283 S:41.8276 W:-126.0131
Temporal Extent: 2000-05-29 - 2002-08-17

Dataset Description

U.S. GLOBEC Northeast Pacific, California Current System
Mesoscale Process Studies Chlorophyll a Data

During juvenile salmonid trawling cruises, additional sampling included CTD profiles, neuston net tows, and chlorophyll a water samples. At most stations, data on all parameters were collected.

Contacts for this data set are:
Dr. Richard Brodeur
Northwest Fisheries Science Center
National Oceanographic and Atmospheric Administration
Newport, OR 97365
Phone: 541-867-0336
Email: rick.brodeur@noaa.gov

Suzan Pool
Cooperative Institute of Marine Resources
Oregon State University
Newport, OR 97365
Phone: 541-867-0195
Email: suzan.pool@noaa.gov


Methods & Sampling

Replicate samples for in-vitro chlorophyll a were collected from 3-m depth with a 1-l Niskin water sampler. Sampling done at all stations at which salmon trawling was done; additional sampling at most stations was a CTD, plankton sampling.


Data Processing Description

Samples were immediately filtered through GF/F glass fiber filters, then frozen for further analysis in the laboratory. One of two replicates was processed whereas the other was a back up sample. Chlorophyll a was processed using the cold-acetone extraction method and measured with a Turner Designs 10-AU fluorometer (Arar and Collins, 1997).


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Data Files

File
chl_a_3m.csv
(Comma Separated Values (.csv), 33.92 KB)
MD5:9538fbfb73d628e26480cbaa60b0d569
Primary data file for dataset ID 2463

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Related Publications

Arar, E. J. AND G. B. COLLINS. Method 445.0 In Vitro Determination of Chlorophyll a and Pheophytin ain Marine and Freshwater Algae by Fluorescence. U.S. Environmental Protection Agency, Washington, DC, 1997. https://cfpub.epa.gov/si/si_public_record_report.cfm?Lab=NERL&dirEntryId=309417
Methods

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Parameters

ParameterDescriptionUnits
yr

year

dimensionless
cruise_id

cruise ID

dimensionless
cast

cast number within cruise

dimensionless
sta_std

standard station name

dimensionless
lat

latitude (decimal degrees)

decimal degrees
lon

longitude (decimal degrees)

decimal degrees
depth_w

bottom depth of station (meters)

meters
month_local

local month

dimensionless
day_local

local day

dimensionless
time_local

local time (24-hr)

dimensionless
inst

sampling instrument

dimensionless
depth

sample depth (meters)

meters
chl_a

chlorophyll a concentration (ug/L)

ug/L
phaeo

phaeophytin a concentration (ug/L)

ug/L
comments

comments about particular sample

dimensionless
timezone

Time zone, relative to GMT time.

hours
ship

Name of the vessel.

dimensionless


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Instruments

Dataset-specific Instrument Name
Niskin Bottle
Generic Instrument Name
Niskin bottle
Dataset-specific Description
Niskin bottle sample at 3-m depth. Replicate samples for in-vitro chlorophyll a were collected from 3-m depth with a 1-l Niskin water sampler.
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.


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Deployments

SE0005

Website
Platform
F/V Sea Eagle
Report
Start Date
2000-05-29
End Date
2000-06-11
Description
Methods & Sampling
Replicate samples for in-vitro chlorophyll a were collected from 3-m depth with a 1-l Niskin water sampler.

Processing Description
Samples were immediately filtered through GF/F glass fiber filters, then frozen for further analysis in the laboratory. One of two replicates was processed whereas the other was a back up sample. Chlorophyll a was processed using the cold-acetone extraction method and measured with a Turner Designs 10-AU fluorometer (Arar and Collins, 1997).

SE0007

Website
Platform
F/V Sea Eagle
Report
Start Date
2000-07-28
End Date
2000-08-12
Description
Methods & Sampling
Replicate samples for in-vitro chlorophyll a were collected from 3-m depth with a 1-l Niskin water sampler.

Processing Description
Samples were immediately filtered through GF/F glass fiber filters, then frozen for further analysis in the laboratory. One of two replicates was processed whereas the other was a back up sample. Chlorophyll a was processed using the cold-acetone extraction method and measured with a Turner Designs 10-AU fluorometer (Arar and Collins, 1997).

FR0206-01

Website
Platform
F/V Frosti
Report
Start Date
2002-05-31
End Date
2002-06-08
Description
Event logs provide an overall summary of the sampling activities during a cruise. A hard copy of the event log is also included in the cruise report. Further documentation about event logs is available in Chief Scientist Data Reporting Requirements. For further information contact the Data Management Office Last updated November 03, 2006; gfh 20 May 2011, dld - This cruise consisted of Leg 1 and Leg 2. Metadata is edited to reflect this information which was gleaned from the event log and the cruise report. Leg 1 departed Astoria, OR late on 31 May and ended with a brief port stop in Newport, OR to exchange some science personnel and take on supplies on 8 June. The Chief Scientist was Robert Emmett. Leg 2 began late in the afternoon of 8 June departing from Newport, OR and ended 18 June in Newport, OR. The Chief Scientist was Richard Brodeur.

Methods & Sampling
Replicate samples for in-vitro chlorophyll a were collected from 3-m depth with a 1-l Niskin water sampler.

Processing Description
Samples were immediately filtered through GF/F glass fiber filters, then frozen for further analysis in the laboratory. One of two replicates was processed whereas the other was a back up sample. Chlorophyll a was processed using the cold-acetone extraction method and measured with a Turner Designs 10-AU fluorometer (Arar and Collins, 1997).

FR0208

Website
Platform
F/V Frosti
Report
Start Date
2002-08-01
End Date
2002-08-17
Description
Methods & Sampling
Replicate samples for in-vitro chlorophyll a were collected from 3-m depth with a 1-l Niskin water sampler.

Processing Description
Samples were immediately filtered through GF/F glass fiber filters, then frozen for further analysis in the laboratory. One of two replicates was processed whereas the other was a back up sample. Chlorophyll a was processed using the cold-acetone extraction method and measured with a Turner Designs 10-AU fluorometer (Arar and Collins, 1997).

FR0206-02

Website
Platform
F/V Frosti
Report
Start Date
2002-06-08
End Date
2002-06-18
Description
Event logs provide an overall summary of the sampling activities during a cruise. A hard copy of the event log is also included in the cruise report. Further documentation about event logs is available in Chief Scientist Data Reporting Requirements. For further information contact the Data Management Office Last updated November 03, 2006; gfh 20 May 2011, dld - This cruise consisted of Leg 1 and Leg 2. Metadata is edited to reflect this information which was gleaned from the event log and the cruise report. Leg 1 departed Astoria, OR late on 31 May and ended with a brief port stop in Newport, OR to exchange some science personnel and take on supplies on 8 June. The Chief Scientist was Robert Emmett. Leg 2 began late in the afternoon of 8 June departing from Newport, OR and ended 18 June in Newport, OR. The Chief Scientist was Richard Brodeur.

Methods & Sampling
Replicate samples for in-vitro chlorophyll a were collected from 3-m depth with a 1-l Niskin water sampler.

Processing Description
Samples were immediately filtered through GF/F glass fiber filters, then frozen for further analysis in the laboratory. One of two replicates was processed whereas the other was a back up sample. Chlorophyll a was processed using the cold-acetone extraction method and measured with a Turner Designs 10-AU fluorometer (Arar and Collins, 1997).


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Project Information

U.S. GLOBEC Northeast Pacific (NEP)


Coverage: Northeast Pacific Ocean, Gulf of Alaska


Program in a Nutshell

Goal: To understand the effects of climate variability and climate change on the distribution, abundance and production of marine animals (including commercially important living marine resources) in the eastern North Pacific. To embody this understanding in diagnostic and prognostic ecosystem models, capable of capturing the ecosystem response to major climatic fluctuations.

Approach: To study the effects of past and present climate variability on the population ecology and population dynamics of marine biota and living marine resources, and to use this information as a proxy for how the ecosystems of the eastern North Pacific may respond to future global climate change. The strong temporal variability in the physical and biological signals of the NEP will be used to examine the biophysical mechanisms through which zooplankton and salmon populations respond to physical forcing and biological interactions in the coastal regions of the two gyres. Annual and interannual variability will be studied directly through long-term observations and detailed process studies; variability at longer time scales will be examined through retrospective analysis of directly measured and proxy data. Coupled biophysical models of the ecosystems of these regions will be developed and tested using the process studies and data collected from the long-term observation programs, then further tested and improved by hindcasting selected retrospective data series.



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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).



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Funding

Funding SourceAward
NSF Division of Ocean Sciences (NSF OCE)
National Oceanic and Atmospheric Administration (NOAA)

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