Picophytoplankton abundances of live samples determined by flow cytometry (shipboard analysis) on R/V Melville cruise MV1008 in the Costa Rica Dome in 2010 (CRD FLUZiE project)

Website: https://www.bco-dmo.org/dataset/516327
Data Type: Cruise Results
Version: 1
Version Date: 2014-06-02

Project
» Costa Rica Dome FLUx and Zinc Experiments (CRD FLUZiE)

Programs
» Integrated Marine Biogeochemistry and Ecosystem Research -US (IMBER-US)
» Ocean Carbon and Biogeochemistry (OCB)
ContributorsAffiliationRole
Landry, Michael R.University of California-San Diego Scripps (UCSD-SIO)Principal Investigator
Selph, Karen E.University of Hawaiʻi at Mānoa (SOEST)Contact
Rauch, ShannonWoods Hole Oceanographic Institution (WHOI BCO-DMO)BCO-DMO Data Manager

Abstract
Picophytoplankton abundances from live samples were analyzed within 1-3 hrs on a Beckman-Coulter EPIC XL flow cytometer. Cell populations include Synechococcus and Photosynthetic Eukaryotes. Samples were collected on the MV1008 cruise in the Costa Rica Dome (CRD) region of the Eastern Tropical Pacific Ocean.


Coverage

Spatial Extent: N:10.2998 E:-86.735 S:6.6219 W:-92.9871
Temporal Extent: 2010-06-24 - 2010-07-24

Dataset Description

Picophytoplankton abundances from live samples were analyzed within 1-3 hrs on a Beckman-Coulter EPIC XL flow cytometer. Cell populations include Synechococcus and Photosynthetic Eukaryotes. Samples were collected on the MV1008 cruise in the Costa Rica Dome (CRD) region of the Eastern Tropical Pacific Ocean.


Methods & Sampling

Samples were collected from the CTD-Rosette PVC Niskin bottles, kept on ice in the dark until analyzed within 1-3 hr on a Beckman-Coulter EPICS XL flow cytometer, equipped with one 488 nm 1 mW laser for excitation. Samples (2.2 mL) were delivered quantitatively to the instrument using an Orion syringe pump, at a rate of 0.44 mL per minute. Signals from the Chlorophyll (680±20 nm), Phycoerythrin (575±20 nm), and the forward and side scatter detectors were used to delineate Synechococcus, and Photosynthetic eukaryotes. Calibration beads (6 um and 20 um yellow-green beads) were used to normalize cellular fluorescence values and assure optimal instrument settings. Raw data files (listmode) were processed in FlowJo software (Treestar Inc.).


Data Processing Description

Raw data, representing 2.2 mL of sample, was corrected for run volume, to arrive at cellular concentrations (cells/mL).


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Data Files

File
picophyto_fcm_ship.csv
(Comma Separated Values (.csv), 16.12 KB)
MD5:d4ec1aa3388e7afbfd34375400e89d9e
Primary data file for dataset ID 516327

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Parameters

ParameterDescriptionUnits
event

Number referring to the particular activity (event) on the FluZiE cruise.

integer
cast

CTD Cast number from the FluZiE cruise.

integer
niskin

Niskin bottle that the sample was taken from.

integer
date_local

Date of CTD cast (local time zone of UTC -6). in the format mmddyyyy

unitless
lon

Longitude in degrees East.

decimal degrees
lat

Latitude in degrees North.

decimal degrees
depth

Sample depth.

meters
cycle

Type and number of cruise sampling event. Either "Stn_n" or "Cycle_n". A transect of stations was sampled from 29 June to 03 July. Five quasi-Lagrangian experiments called "cycles" were conducted during the remainder of the cruise.

text
coccus_s

Abundance of Synechococcus abundance.

cells per milliliter (cells/mL)
peuk

Abundance of Photosynthetic Eukaryotes.

cells per milliliter (cells/mL)


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Instruments

Dataset-specific Instrument Name
Beckman-Coulter Altra flow cytometer
Generic Instrument Name
Flow Cytometer
Dataset-specific Description
Samples were run on a Beckman-Coulter Altra flow cytometer, equipped with one 488 nm 1W laser for excitation.
Generic Instrument Description
Flow cytometers (FC or FCM) are automated instruments that quantitate properties of single cells, one cell at a time. They can measure cell size, cell granularity, the amounts of cell components such as total DNA, newly synthesized DNA, gene expression as the amount messenger RNA for a particular gene, amounts of specific surface receptors, amounts of intracellular proteins, or transient signalling events in living cells. (from: http://www.bio.umass.edu/micro/immunology/facs542/facswhat.htm)

Dataset-specific Instrument Name
Niskin bottle
Generic Instrument Name
Niskin bottle
Dataset-specific Description
Samples were collected from the CTD-Rosette PVC Niskin bottles.
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

MV1008

Website
Platform
R/V Melville
Report
Start Date
2010-06-22
End Date
2010-07-25
Description
Research on the cruise was aimed at acquiring a better understanding of plankton dynamics, carbon and nutrient fluxes, and potential trace element limitation in the Costa Rica Dome region of the eastern tropical Pacific. The specific science objectives were: 1) to assess grazing and trace metal/nutrient controls on primary production and phytoplankton standing stocks; 2) to quantify carbon and elemental fluxes and export rates from the euphotic zone; and 3) to measure microbial population, processes, stable isotope abundances associated with the OMZ and nitrite maxima. Operations included: 4-day sediment trap deployments, daily process experiments conducted on satellite-tracked drifters, CTD and trace-metal rosette sampling, shipboard grow-out experiments, net sampling for zooplankton biomass and grazing assessments, and MOCNESS stratified tows to 1000 m. BCO-DMO Note: March 2013 (CLC): The original CTD profile data (85 casts) have been submitted by R2R to NODC.  Jim Moffett (USC) was a participant on this cruise and is interested in getting a copy of the full set of CTD cast data (deep and shallow casts). He plans to contact SIO ODF group or Mike Landry (Chief Scientist). Original cruise data are available from the NSF R2R data catalog.


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Project Information

Costa Rica Dome FLUx and Zinc Experiments (CRD FLUZiE)

Coverage: Costa Rica Dome, Eastern Tropical Pacific Ocean


Research was aimed at improved understanding of plankton dynamics, carbon and nutrient fluxes, and potential trace element limitation in the Costa Rica Dome region of the eastern tropical Pacific. The specific science objectives of the 2010 R/V Melville cruise (MV1008) were:
1) to assess grazing and trace metal/nutrient controls on primary production and phytoplankton standing stocks;
2) to quantify carbon and elemental fluxes and export rates from the euphotic zone; and
3) to measure microbial population, processes, stable isotope abundances associated with the OMZ and nitrite maxima.

Additional information about MV1008 can be found in the cruise report (PDF).

NOTE: The original proposal and award abstract are not relevant. The project was originally funded by NSF as experimental tests of phytoplankton controls in the Arabian Sea. Piracy concerns in the region led to the cancellation of the research cruise in 2009, and a Change of Scope request was approved to focus the project on related issues in the Costa Rica Dome (CRD).

Though this project is not formally affiliated with any large program, it aligns with IMBER's emphasis on community ecology and biogeochemistry, and the OCB focus on carbon-based measurements of production, grazing and export processes.



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Program Information

Integrated Marine Biogeochemistry and Ecosystem Research -US (IMBER-US)


Coverage: global


The BCO-DMO database includes data from IMBER endorsed projects lead by US funded investigators. There is no dedicated US IMBER project or data management office. Those functions are provided by US-OCB and BCO-DMO respectively.

The information in this program description pertains to the Internationally coordinated IMBER research program. The projects contributing data to the BCO-DMO database are those funded by US NSF only. The full IMBER data catalog is hosted at the Global Change Master Directory (GCMD). 

IMBER Data Portal: The IMBER project has chosen to create a metadata portal hosted by the NASA's Global Change Master Directory (GCMD). The GCMD IMBER data catalog provides an overview of all IMBER endorsed and related projects and links to datasets, and can be found at URL http://gcmd.nasa.gov/portals/imber/.

IMBER research will seek to identify the mechanisms by which marine life influences marine biogeochemical cycles, and how these, in turn, influence marine ecosystems. Central to the IMBER goal is the development of a predictive understanding of how marine biogeochemical cycles and ecosystems respond to complex forcings, such as large-scale climatic variations, changing physical dynamics, carbon cycle chemistry and nutrient fluxes, and the impacts of marine harvesting. Changes in marine biogeochemical cycles and ecosystems due to global change will also have consequences for the broader Earth System. An even greater challenge will be drawing together the natural and social science communities to study some of the key impacts and feedbacks between the marine and human systems.

To address the IMBER goal, four scientific themes, each including several issues, have been identified for the IMBER project: Theme 1 - Interactions between Biogeochemical Cycles and Marine Food Webs; Theme 2 - Sensitivity to Global Change: How will key marine biogeochemical cycles, ecosystems and their interactions, respond to global change?; Theme 3 - Feedback to the Earth System: What are the roles of the ocean biogeochemistry and ecosystems in regulating climate?; and Theme 4 - Responses of Society: What are the relationships between marine biogeochemical cycles, ecosystems, and the human system?


Ocean Carbon and Biogeochemistry (OCB)


Coverage: Global


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.



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Funding

Funding SourceAward
NSF Division of Ocean Sciences (NSF OCE)

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