Contributors | Affiliation | Role |
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Menden-Deuer, Susanne | University of Rhode Island (URI-GSO) | Principal Investigator |
Franzè, Gayantonia | University of Rhode Island (URI-GSO) | Scientist |
Rauch, Shannon | Woods Hole Oceanographic Institution (WHOI BCO-DMO) | BCO-DMO Data Manager |
See complete methodology in Franzè and Menden-Deuer, 2020.
Clonal cultures of Oxyrrhis marina (CCMP 3375), Gyrodinium dominans (SPMC 103), and Protoperidinium bipes were established from single-cell isolation. Herbivorous protists were acclimated to each target temperature before growth rates were measured. Due to the wide temperature range tested (0−22°C), cultures were moved from the initial temperature of 15°C through gradual transitions limited to at most 3°C. The experimental Day 0 (D0) was defined as the first day on which acclimated growth rates were measured. To determine predator and prey abundance, samples were preserved in acid Lugol at a 2% final concentration (Menden-Deuer et al. 2001) and enumerated using a Sedgewick-Rafter slide (1 ml volume) and a Nikon Eclipse E800 light microscope equipped with phase contrast. Herbivore biovolume was calculated based on linear dimensions obtained from ≥35 cells measured at each time point and temperature treatment using an image analysis system consisting of a high-resolution digital camera (Allied Vision, Stingray F45) and ImageJ software (version 1.5i).
Growth rates of the 3 herbivorous species were determined at 7 incubation temperatures: 0, 2, 5, 10, 15, 18, and 22°C. Changes in O. marina, G. dominans, and P. bipes abundance and biomass were determined over 24 h incubations of the triplicate 150 ml bottles and used to calculate growth rates (μ d−1) assuming exponential growth: μ = ln(Nt/N0)/t, where: N0 and Nt are the initial and final cell abundance (or biomass) respectively, and t is the experiment duration in days. Measurements were made at Day 0 and again after 10 and 30 days.
Statistical analyses were performed using R (version 1.2.1335) and Prism 7.
BCO-DMO Processing:
- renamed fields to comply with BCO-DMO naming conventions;
- replaced "NM" with "nd" (no data).
File |
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temp_dependent_biovolume.csv (Comma Separated Values (.csv), 4.73 KB) MD5:dcfd55da92fb427d72fd5a0964ce0d2b Primary data file for dataset ID 857328 |
Parameter | Description | Units |
Event | cell imaged to determine size | unitless |
Species | Name of the species used for the experiment | unitless |
ESD_um3_0C | Equivalent spherical diameter at incubation temperature of 0 degrees Celsius | cubic micrometer (um^3) |
ESD_um3_2C | Equivalent spherical diameter at incubation temperature of 2 degrees Celsius | cubic micrometer (um^3) |
ESD_um3_5C | Equivalent spherical diameter at incubation temperature of 5 degrees Celsius | cubic micrometer (um^3) |
ESD_um3_10C | Equivalent spherical diameter at incubation temperature of 10 degrees Celsius | cubic micrometer (um^3) |
ESD_um3_15C | Equivalent spherical diameter at incubation temperature of 15 degrees Celsius | cubic micrometer (um^3) |
ESD_um3_18C | Equivalent spherical diameter at incubation temperature of 18 degrees Celsius | cubic micrometer (um^3) |
ESD_um3_22C | Equivalent spherical diameter at incubation temperature of 22 degrees Celsius | cubic micrometer (um^3) |
Dataset-specific Instrument Name | Allied Vision, Stingray F45 |
Generic Instrument Name | Camera |
Dataset-specific Description | Cell measurements were performed using a high-resolution digital camera (Allied Vision, Stingray F45) and ImageJ software (version 1.5i). |
Generic Instrument Description | All types of photographic equipment including stills, video, film and digital systems. |
Dataset-specific Instrument Name | I-36LLVL Series, Percival Scientific |
Generic Instrument Name | In-situ incubator |
Dataset-specific Description | Experiments were conducted using temperature-controlled incubators (I-36LLVL Series, Percival Scientific). |
Generic Instrument Description | A device on a ship or in the laboratory that holds water samples under controlled conditions of temperature and possibly illumination. |
Dataset-specific Instrument Name | Nikon Eclipse E800 light microscope |
Generic Instrument Name | Microscope - Optical |
Dataset-specific Description | Microscopy counts were performed with a Nikon Eclipse E800 light microscope. |
Generic Instrument Description | Instruments that generate enlarged images of samples using the phenomena of reflection and absorption of visible light. Includes conventional and inverted instruments. Also called a "light microscope". |
NSF Award Abstract:
Plankton, single-celled organisms that inhabit the world's oceans are responsible for the generation of oxygen, cycling energy and matter between the atmosphere and the deep ocean and are the basis for virtually all seafood harvested. These life-giving functions critically depend on the relative rates at which plankton grow and get eaten. How temperature influences those rates is essential to understand plankton responses to environmental changes and ocean dynamics. It is well established that plankton grow faster when temperatures are higher however, whether feeding has a similar temperature dependence is unknown. That means oceanographers are missing key data required to build global predictive models. This project will fill essential knowledge gaps and measure physiological rates of singled celled zooplankton across temperature gradients representing the global ocean, from polar to tropical regions and throughout the seasonal cycle. Researchers will combine laboratory experiments with specimens taken from the coastal ocean (Narragansett Bay), which is exemplary in its strong seasonal temperature variations. These data will provide a clear picture of the production capacity and activity of plankton in a global and dynamic ocean. The project supports an early career scientist, as well as graduate and undergraduate students. Scientists will continue communicating their research to the public through large-scale outreach events, education at the high-school level, and engagement through online and other media. Moreover, researchers will continue collaborating with the Metcalf Institute for Marine & Environmental Reporting to support their Annual Science Immersion Workshop for Journalists and their ongoing work to disseminate research findings through web-based seminars.
Grazing is the single largest loss factor of marine primary production and thus affects a key transfer rate between global organic and inorganic matter pools. Remarkably, data for herbivorous protist growth and grazing rates at temperatures representative of the vast polar regions and during winter and spring periods are extremely sparse. By combining laboratory experiments with ground truthing fieldwork, this project alleviates a central knowledge gap in oceanography and delivers the empirical measurements necessary to derive algorithms to incorporate temperature dependence of heterotrophic protist growth and grazing rates into biogeochemical models. The extraordinary seasonal temperature fluctuations in a temperate coastal estuary (Narragansett Bay) are exploited to measure rates of heterotrophic protists isolated from different temperatures and seasons and to quantify the temperature and acclimation responses of these ecotypes. This project delivers data urgently needed to solve the conundrum of whether herbivorous growth and predation is depressed at low temperatures, implying low trophic transfer rates and high carbon export, or if predation proceeds at rates comparable to temperate systems with primary production largely lost to predation. Large temperature gradients in the global ocean mean that cross-biome and biogeochemical models are particularly sensitive to assumptions about the temperature dependence in modeled rate processes. Establishment of the dependence of heterotrophic plankton physiological rates (growth and grazing) to gradients of temperature, mimicking realistic conditions experienced by plankton in a changing ocean, is a key step towards integrating much needed biological information in biogeochemical modeling efforts. This project makes a significant contribution to linking ecological research with ecosystem models by providing empirically rooted algorithms of the temperature dependence of protistan herbivory and growth rates, key processes in the transformation of organic matter in global biogeochemical cycles and tools critically missing in ecosystem models.
Funding Source | Award |
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NSF Division of Ocean Sciences (NSF OCE) |