Eukaryotic phytoplankton flow cytometric results from salp grazing incubations conducted on R/V Tangaroa cruise TAN1810 during Oct-Nov 2018 (NCEI Accession 0278015)
This dataset contains biological and survey - biological data collected on R/V Tangaroa during cruise TAN1810 from 2018-10-23 to 2018-11-21. These data include stage. The instruments used to collect these data include Flow Cytometer, Niskin bottle, and Plankton Net. These data were collected by Michael Stukel of Florida State University, Moira Decima of University of California-San Diego, and Karen E. Selph of University of Hawaii at Manoa as part of the "Collaborative Research: Quantifying trophic roles and food web ecology of salp blooms of the Chatham Rise (Salp Food Web Ecology)" project. The Biological and Chemical Oceanography Data Management Office (BCO-DMO) submitted these data to NCEI on 2022-09-13.
The following is the text of the dataset description provided by BCO-DMO:
Eukaryotic Phytoplankton Flow Cytometry from Salp Incubations
The following is the text of the dataset description provided by BCO-DMO:
Eukaryotic Phytoplankton Flow Cytometry from Salp Incubations
Dataset Citation
- Cite as: Stukel, Michael; Decima, Moira; Selph, Karen E. (2023). Eukaryotic phytoplankton flow cytometric results from salp grazing incubations conducted on R/V Tangaroa cruise TAN1810 during Oct-Nov 2018 (NCEI Accession 0278015). [indicate subset used]. NOAA National Centers for Environmental Information. Dataset. https://www.ncei.noaa.gov/archive/accession/0278015. Accessed [date].
Dataset Identifiers
ISO 19115-2 Metadata
gov.noaa.nodc:0278015
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Ordering Instructions | Contact NCEI for other distribution options and instructions. |
Distributor |
NOAA National Centers for Environmental Information +1-301-713-3277 NCEI.Info@noaa.gov |
Dataset Point of Contact |
NOAA National Centers for Environmental Information ncei.info@noaa.gov |
Time Period | 2018-10-23 to 2018-11-21 |
Spatial Bounding Box Coordinates |
West: 174.095
East: 179.9428
South: -45.5503
North: -42.742
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Data Presentation Form | Digital table - digital representation of facts or figures systematically displayed, especially in columns |
Dataset Progress Status | Complete - production of the data has been completed Historical archive - data has been stored in an offline storage facility |
Data Update Frequency | As needed |
Supplemental Information | Acquisition Description: This dataset seeks to quantify food web flows through contrasting salp-dominated and salp-absent water parcels near the Chatham Rise off western New Zealand where salp blooms are a predictable phenomenon. Paired 20-liter plankton kreisels or 30-liter pseudo-kreisels were gently filled (using silicon tubing) with mixed layer seawater collected by CTD-Niskin rosette casts at ~22:00 local time. Salps for incubations were collected at ~23:00 local time using the salp net. The net was towed slowly and briefly (5-10 minutes) through the mixed layer. Healthy specimens, i.e., those that showed no physical damage, were then gently transferred (using a large ladle) into a bucket containing filtered surface seawater Specimens were further observed (15-30 minutes) to ensure they actively swam (i.e., that they appeared healthy). They were then transferred into one of the paired kreisels (+Salp treatment), while the second kreisel was used as a control treatment with prey only. We successfully collected and incubated S. thompsoni blastozooids and oozooids ranging in size from 50 – 128 millimeters. We also conducted three incubations with a chain of blastozooids (6-8 millimeter individuals) released by an oozooid inside of one of the plankton kreisels. We found that this was the only way to successfully obtain such small blastozooids in healthy conditions. We also incubated a 112-millimeter Thetys vagina oozooid. Water was circulated within the kreisels using a peristaltic pump and silicon tubing. Just after salp transfer to the kreisels, initial samples for flow cytometry were taken from each experimental and control kreisel. Additional time points were taken approximately every 2 hours and analyzed in near real time to allow us to monitor salp grazing. Incubations typically lasted ~24 hours. Samples from the salp incubations were analyzed at sea on a Becton-Dickinson Accuri C6 Plus flow cytometer to estimate the abundance and size of eukaryotic phytoplankton. Samples (~660 µL) were run live within ~1-2 h of collection, discriminating on the Chl a fluorescence signal. We estimated cell diameter from forward light scatter after developing a relationship based on analyses of multiple polystyrene bead sizes (0.99-10 µm diameter). We note that forward scatter is an imperfect proxy for equivalent spherical diameter, and thus the absolute cell sizes determined in our study should be assumed to have associated uncertainty. For additional details on all methods, see Stukel et al. (in review). Note: This dataset is also provided in .mat (MATLAB) format under Supplemental Files. |
Purpose | This dataset is available to the public for a wide variety of uses including scientific research and analysis. |
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Data Center keywords | NODC COLLECTING INSTITUTION NAMES THESAURUS NODC SUBMITTING INSTITUTION NAMES THESAURUS Global Change Master Directory (GCMD) Data Center Keywords |
Platform keywords | NODC PLATFORM NAMES THESAURUS BCO-DMO Platform Names Global Change Master Directory (GCMD) Platform Keywords ICES/SeaDataNet Ship Codes |
Instrument keywords | NODC INSTRUMENT TYPES THESAURUS BCO-DMO Standard Instruments Global Change Master Directory (GCMD) Instrument Keywords Originator Instrument Names |
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Project keywords | BCO-DMO Standard Projects Provider Cruise IDs Provider Funding Award Information |
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Last Modified: 2024-05-31T15:15:28Z
For questions about the information on this page, please email: ncei.info@noaa.gov
For questions about the information on this page, please email: ncei.info@noaa.gov