Contributors | Affiliation | Role |
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Lomas, Michael W. | Bigelow Laboratory for Ocean Sciences | Principal Investigator |
Twining, Benjamin | Bigelow Laboratory for Ocean Sciences | Co-Principal Investigator |
Baer, Steven E. | Bigelow Laboratory for Ocean Sciences | Contact |
Rauch, Shannon | Woods Hole Oceanographic Institution (WHOI BCO-DMO) | BCO-DMO Data Manager |
Phytoplankton diversity along with carbon and nitrogen uptake rates from cruise RR1604 along the GO-SHIP IO9 repeat hydrography section of the Indian Ocean.
All nutrient and cell count methodology is described in the published work coming out of this data set (see below).
Samples were initially collected with a CTD/Niskin rosette, as supplied by the ship.
Urea and total dissolved phosphorus (for calculation of dissolved organic phosphorus) were determined on a Thermo Scientific Genesys 10UV spectrophotometer. See Lomas et al. (2010) for a description of the latter.
Cell counts for heterotrophic bacteria and nanoplankton (<20 um) cells were performed on a BD FACSJazz flow cytometer, using standard methods and 0.53 um bead stocks for reference material. Visualization of heterotrophic bacteria was performed with SYBR Green stain.
Biomass calculations were derived from flow cytometry data output, as per Casey et al. (2013).
Larger (>20 um) autotrophs were enumerated on a FlowCam (Fluid Imagining Technologies).
Biomass and isotopic enrichment, used to calculate specific and absolute uptake rates, were assessed on a Thermo Finnegan Delta V mass spectrometer, as operated by the Bigelow Analytical Services team.
Sample accuracy was assessed by using certified standards, for those measurements where standards are available. Certified standards were run with each analytical run and compared to long term control charts for respective analyses. For those analyses where there are no standards (e.g., flow cytometric cell counts) data were assessed for reasonableness based upon extensive experience of the PI’s.
Data processing was performed using mostly Microsoft Excel. Further statistical analyses and graphing were performed with SigmaPlot. All samples collected are included in the report. Any occurences of "nd" in the data mean those samples were not collected.
BCO-DMO Processing:
- modified parameter names to conform with BCO-DMO naming convetions (removed units, replaced spaces with underscores);
- replaced blank cells with "nd" ("no data").
File |
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IO_Phytoplankton.csv (Comma Separated Values (.csv), 9.99 KB) MD5:184fcb3dcf42c7c339764b0935bf81da Primary data file for dataset ID 723191 |
Parameter | Description | Units |
station | Station number | unitless |
latitude | Station latitude; positive values = North | decimal degrees |
longitude | Station longitude; positive values = East | decimal degrees |
depth | Sample depth | meters (m) |
urea | Urea concentration. BD = below detection (the detection limit for the urea method is 0.01 umol L-1). | micromoles per liter (umol L-1) |
DOP | Dissolved organic phosphorus concentration | micromoles per liter (umol L-1) |
chlorophyll_a | Chlorophyll a | milligrams per cubic meter (mg m-3) |
LNA_bacteria | Count of low-nucleic acid heterotrophic bacteria | cells per milliliter (cells ml-1) |
HNA_bacteria | Count of high-nucleic acid heterotrophic bacteria | cells per milliliter (cells ml-1) |
prochlorococcus | Count of Prochlorococcus cells | cells per milliliter (cells ml-1) |
synechococcus | Count of Synechococcus cells | cells per milliliter (cells ml-1) |
picoeukaryotes | Count of picoeukaryote (<3 um) cells | cells per milliliter (cells ml-1) |
nanoeukaryotes | Count of nanoeukaryote (3-20 um) cells | cells per milliliter (cells ml-1) |
bacteria_biomass | Biomass of all bacteria | micrograms carbon per liter (ug C L-1) |
prochlorococcus_biomass | Carbon content of Prochlorococcus cells | micrograms carbon per liter (ug C L-1) |
synechococcus_biomass | Carbon content of Synechococcus cells | micrograms carbon per liter (ug C L-1) |
small_eukaryote_biomass | Carbon content of picoeukaryote and nanoeukaryote cells | micrograms carbon per liter (ug C L-1) |
diatom_biomass | Carbon content of diatoms | micrograms carbon per liter (ug C L-1) |
dinoflagellate_biomass | Carbon content of dinoflagellates | micrograms carbon per liter (ug C L-1) |
ciliate_biomass | Carbon content of ciliates | micrograms carbon per liter (ug C L-1) |
other_large_phyto_biomass | Carbon content of >20 um phytoplankton not included in other categories | micrograms carbon per liter (ug C L-1) |
NO3_V | Nitrate specific uptake | per hour (h-1) |
NO3_V_std_dev | Standard deviation of NO3_V | per hour (h-1) |
NO3_rho | Nitrate absolute uptake | nanomoles per liter per hour (nmol N L-1 h-1) |
NO3_rho_std_dev | standard deviation of NO3_rho | nanomoles per liter per hour (nmol N L-1 h-1) |
NH4_V | Ammonium specific uptake | per hour (h-1) |
NH4_V_std_dev | Standard deviation of NH4_V | per hour (h-1) |
NH4_rho | Ammonium absolute uptake | nanomoles per liter per hour (nmol N L-1 h-1) |
NH4_rho_std_dev | Standard deviation of NH4_rho | nanomoles per liter per hour (nmol N L-1 h-1) |
urea_V | Urea specific uptake | per hour (h-1) |
urea_V_std_dev | Standard deviation of urea V | per hour (h-1) |
urea_rho | Urea absolute uptake | nanomoles per liter per hour (nmol N L-1 h-1) |
urea_rho_std_dev | Standard deviation of urea rho | nanomoles per liter per hour (nmol N L-1 h-1) |
C_V | Bicarbonate specific uptake | per hour (h-1) |
C_V_std_dev | Standard deviation of Bicarbonate specific uptake | per hour (h-1) |
C_rho | Bicarbonate absolute uptake | nanomoles per liter per hour (nmol N L-1 h-1) |
C_rho_std_dev | Standard deviation of C rho | nanomoles per liter per hour (nmol N L-1 h-1) |
Dataset-specific Instrument Name | CTD/Niskin rosette |
Generic Instrument Name | CTD - profiler |
Generic Instrument Description | The Conductivity, Temperature, Depth (CTD) unit is an integrated instrument package designed to measure the conductivity, temperature, and pressure (depth) of the water column. The instrument is lowered via cable through the water column. It permits scientists to observe the physical properties in real-time via a conducting cable, which is typically connected to a CTD to a deck unit and computer on a ship. The CTD is often configured with additional optional sensors including fluorometers, transmissometers and/or radiometers. It is often combined with a Rosette of water sampling bottles (e.g. Niskin, GO-FLO) for collecting discrete water samples during the cast.
This term applies to profiling CTDs. For fixed CTDs, see https://www.bco-dmo.org/instrument/869934. |
Dataset-specific Instrument Name | BD FACSJazz flow cytometer |
Generic Instrument Name | Flow Cytometer |
Dataset-specific Description | Cell counts for heterotrophic bacteria smaller ( |
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 | Thermo Finnegan Delta V mass spectrometer |
Generic Instrument Name | Mass Spectrometer |
Dataset-specific Description | Biomass and isotopic enrichment, used to calculate specific and absolute uptake rates, were assessed on a Thermo Finnegan Delta V mass spectrometer, as operated by the Bigelow Analytical Services team. |
Generic Instrument Description | General term for instruments used to measure the mass-to-charge ratio of ions; generally used to find the composition of a sample by generating a mass spectrum representing the masses of sample components. |
Dataset-specific Instrument Name | CTD/Niskin rosette |
Generic Instrument Name | Niskin bottle |
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. |
Dataset-specific Instrument Name | Thermo Scientific Genesys 10UV spectrophotometer |
Generic Instrument Name | Spectrophotometer |
Dataset-specific Description | Urea and total dissolved phosphorus (for calculation of dissolved organic phosphorus) were determined on a Thermo Scientific Genesys 10UV spectrophotometer. |
Generic Instrument Description | An instrument used to measure the relative absorption of electromagnetic radiation of different wavelengths in the near infra-red, visible and ultraviolet wavebands by samples. |
Website | |
Platform | R/V Roger Revelle |
Start Date | 2016-03-21 |
End Date | 2016-04-28 |
Description from NSF award abstract:
The Indian Ocean accounts for nearly a fifth of global ocean photosynthesis and is likely a key component in global ocean nutrient and carbon cycles. However, the Indian Ocean may be the least studied major marine body on the planet. Our limited understanding suggests extensive variations in physical and chemical environmental conditions, but how this variation influences biodiversity, nutrient stress, and more broadly regional differences in the functioning of phytoplankton is unknown. To help address these gaps, the investigators will conduct a study by joining an already-funded major research cruise to this region. It will cover a northern region with some of the highest temperatures recorded in open ocean waters, an area around 10°S of predicted (but not tested in situ) iron stress, and a southern subtropical gyre with unique nitrogen to phosphorous(or N:P) ratios. The focus of this project is to quantify and synthesize the interconnectedness of environmental conditions, phytoplankton diversity and genome content, and nutrient biogeochemistry, with the goal of understanding how these may lead to unique biogeochemical regions in Indian Ocean. The research will have broader impacts on many levels. First, it will increase public awareness of the role of phytoplankton on ocean functioning, climate, and people's lives through a new partnership with the Aquarium of the Pacific (AOP), which is the fourth most-attended aquarium in the nation. Secondly, the project will train a postdoctoral scholar as well as a graduate and undergraduate students. Third, the research will dramatically increase our basic knowledge ocean biogeochemistry and in many cases will be the first measurements of their kind made in the Indian Ocean.
This project will address two major questions: How do environmental conditions, phytoplankton diversity, phytoplankton physiology, and biogeochemistry vary across the central Indian Ocean? Are there distinct biogeochemical regimes in the central IO? The researchers hypothesize that environmental conditions, including the relative availability of nitrogen (N) and iron (Fe), lead to three distinct phytoplankton communities and biogeochemical regimes. They will employ a series of advanced analytical tools including high sensitivity measurements of dissolved and particulate nutrients (nitrogen, phosphorus, and iron), genomics, bioassays to test for nutrient stress, and cell-sorting of specific taxa followed by measures of nutrient content and uptake. A focus of this project is to quantify and synthesize the interconnectedness of environmental conditions, phytoplankton diversity and genome content, and nutrient biogeochemistry, and how these lead to unique biogeochemical regions in Indian Ocean. This extensive set of observations can ultimately be linked to ocean models and satellite data to provide a comprehensive view of regional differences in chemistry, biodiversity and phytoplankton biogeochemical functioning in the Indian Ocean.
Funding Source | Award |
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NSF Division of Ocean Sciences (NSF OCE) |