Contributors | Affiliation | Role |
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Goetze, Erica | University of Hawaiʻi at Mānoa (SOEST) | Principal Investigator |
Lenz, Petra H. | University of Hawaiʻi at Mānoa (SOEST) | Co-Principal Investigator |
Selph, Karen E. | University of Hawaiʻi at Mānoa (SOEST) | Co-Principal Investigator |
Copley, Nancy | Woods Hole Oceanographic Institution (WHOI BCO-DMO) | BCO-DMO Data Manager |
Five combined bottle incubation and seawater dilution experiments were performed over a two-week period where the in-situ 2-35 µm total cell biomass ranged from 37 – 158 µg C L-1. Both Parvocalanus crassirostris and Bestiolina similis grazed a range of prey types and sizes, and shifted their selectivity of prey groups over the two-week period. In general, P. crassirostris grazed on a wider spectrum of prey than B. similis, which avoided the smallest potential prey (2-5 µm) across all dates. Both species had similar overall grazing rates as well as high daily carbon rations (at times >100%), and selected for the largest cells when they were more abundant. The trophic impact of each species was driven largely by in situ nauplius abundance, which was higher for P. crassirostris, from 0.8 to 8.9 nauplii L-1, than for B. similis, which ranged from 0.2 to 0.8 nauplii L-1. Our results suggest that the two species overlap in their potential prey, however, P. crassirostris appears to target a wider variety of prey, with B. similis preferring larger cells.
BCO-DMO Processing:
- added conventional header with dataset name, PI name, version date, reference information
- renamed parameters to BCO-DMO standard
- reformatted date from d-Mon-yy to yyyy-mm-dd
- transformed table rows and columns
- added lat/lon columns
File |
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physical_KB.csv (Comma Separated Values (.csv), 385 bytes) MD5:76c3d31c75517c35fbe9e9a1cb463b8f Primary data file for dataset ID 637695 |
Parameter | Description | Units |
date_local | local date | yyyy-mm-dd |
lat | latitude; north is positive | decimal degrees |
lon | longitude; east is positive | decimal degrees |
irradiance | solar irradiance as measured at HIMB | uE/sec/m^2 |
wind_spd | wind speed | knots |
wind_dir | wind direction: N=north; S=south; E=east; W=west | unitless |
sal | salinity at 2 meters depth | PSU |
temp | water temperature | degees Celsius |
chl_a | chlorophyll | micrograms/liter |
chl_std_err | chlorophyll standard error | micrograms/liter |
Dataset-specific Instrument Name | |
Generic Instrument Name | Anemometer |
Generic Instrument Description | An anemometer is a device for measuring the velocity or the pressure of the wind. It is commonly used to measure wind speed. Aboard research vessels, it is often mounted with other meteorological instruments and sensors. |
Dataset-specific Instrument Name | |
Generic Instrument Name | Flow Cytometer |
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 | |
Generic Instrument Name | Fluorometer |
Generic Instrument Description | A fluorometer or fluorimeter is a device used to measure parameters of fluorescence: its intensity and wavelength distribution of emission spectrum after excitation by a certain spectrum of light. The instrument is designed to measure the amount of stimulated electromagnetic radiation produced by pulses of electromagnetic radiation emitted into a water sample or in situ. |
Dataset-specific Instrument Name | |
Generic Instrument Name | Photosynthetically Available Radiation Sensor |
Generic Instrument Description | A PAR sensor measures photosynthetically available (or active) radiation. The sensor measures photon flux density (photons per second per square meter) within the visible wavelength range (typically 400 to 700 nanometers). PAR gives an indication of the total energy available to plants for photosynthesis. This instrument name is used when specific type, make and model are not known. |
Dataset-specific Instrument Name | |
Generic Instrument Name | Water Temperature Sensor |
Generic Instrument Description | General term for an instrument that measures the temperature of the water with which it is in contact (thermometer). |
Website | |
Platform | lab UHawaii_SOEST |
Start Date | 2012-03-16 |
End Date | 2013-06-05 |
Description | microzooplankton studies |
Description from NSF Award Abstract:
The most abundant metazoans in the open sea are often the earliest developmental stages of copepods, their nauplii. Nauplii remain under-studied due to the limitations of conventional techniques and an historical emphasis on studying the larger mesozooplankton. However, there is increasing recognition that nauplii play important roles in food web dynamics, and considerable evidence that nauplii may be important trophic intermediaries between microbial and classical food webs due to their high abundance, high weight-specific ingestion rates, and ability to feed on relatively small particles. This team of investigators is developing a novel molecular approach to studying diverse populations of nauplii in mixed field samples based on quantitative Polymerase Chain Reaction (qPCR). They propose to complete development and validation of this qPCR-based technique for enumeration of nauplii, and evaluate its utility in the field. The specific objectives of this research are to identify and reduce technical and biological sources of error in the methodology, determine the accuracy of the method across a range of environmental conditions, and complete one paired field experiment that compares the grazing impact of naupliar and protozoan micro-grazers in a model subtropical coastal ecosystem.
Note: This project is funded by an NSF EAGER award.
Related publications:
Jungbluth, M.J., Goetze, E., and Lenz, P.H. 2013. Measuring copepod naupliar abundance in a subtropical bay using quantitative PCR. Marine Biology, 160: 3125-3141. doi: 10.1007/s00227-013-2300-y
Jungbluth, M.J., and Lenz, P.H. 2013. Copepod diversity in a subtropical bay based on a fragment of the mitochondrial COI gene. Journal of Plankton Research, 35(3): 630-643. doi: 10.1093/plankt/fbt015
Funding Source | Award |
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NSF Division of Ocean Sciences (NSF OCE) |