Contributors | Affiliation | Role |
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Bochdansky, Alexander B. | Old Dominion University (ODU) | Principal Investigator |
Copley, Nancy | Woods Hole Oceanographic Institution (WHOI BCO-DMO) | BCO-DMO Data Manager |
For methodology, see Bochdansky, A. B., M. A. Clouse, G. J. Herndl (2016). (exerpt: PDF)
For Medea 2 Oligonucleotide probe sequences and evaluation details, see Supplemental Files. (PDF)
Raw lengths were converted into micrometers using a calibration curve with relative object distance. The calibration equation is =uncorrected length/(1+0.00893*(object distance/1000)).
BCO-DMO Processing:
- added conventional header with dataset name, PI name, version date, reference information
- renamed parameters to BCO-DMO standard
- transformed Word doc table to flat files
- added lat and lon columns
File |
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CARD_FISH_30um_filter.csv (Comma Separated Values (.csv), 3.28 KB) MD5:68f3362ec738fae4340a46eea9ae5888 Primary data file for dataset ID 658821 |
File |
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Medea 2 Oligonucleotide probe sequences and evaluation details filename: MEDEA_II_cardfish_Oligonucleotide_probe_sequences_eval.pdf (Portable Document Format (.pdf), 155.38 KB) MD5:17521da3260bebaf8c8f2c387695ea1d |
Parameter | Description | Units |
filter_name | Sample label (filter name) indicating the station and pore size of filter | unitless |
station | Station number | unitless |
lat | Latitude; north is positive | decimal degrees |
lon | Longitude; east is positive | decimal degrees |
pore_size | Filter pore size | micrometers (um) |
EKD_NEN | Normalized eukaryote numbers (NEN); number of eukaryotes counted using the EKD probes combined divided by the number of prokaryotes counted using DAPI counter stain | ratio |
EKD_RER | Relative enrichment ratios (RER) of eukaryotes over prokaryotes on the 30 micrometer pore-size filters versus 0.2 micrometer pore-size filters; mathematically: NEN on the 30 micron filter divided by the NEN on the 0.2 micron filters for all eukaryotes | ratio |
Kin_NEN | Normalized eukaryote numbers (NEN); number of kinetoplastids counted using the KIN516 probe divided by the number of prokaryotes counted using DAPI counter stain | ratio |
Kin_RER | Relative enrichment ratios (RER) of kinetoplastids over prokaryotes on the 30 micrometer pore-size filters versus 0.2 micrometer pore-size filters; mathematically: NEN on the 30 micron filter divided by the NEN on the 0.2 micron filters for kinetoplastids | ratio |
LabY_NEN | Normalized eukaryote numbers (NEN); number of labyrithulomycetes counted using the LabY probe divided by the number of prokaryotes counted using DAPI counter stain | ratio |
LabY_RER | Relative enrichment ratios (RER) of labyrithulomycetes over prokaryotes on the 30 micrometer pore-size filters versus 0.2 micrometer pore-size filters; mathematically: NEN on the 30 micron filter divided by the NEN on the 0.2 micron filters for labyrithulomycetes | ratio |
PF2_NEN | Normalized eukaryote numbers (NEN); number of fungi counted using the PF2 probe divided by the number of prokaryotes counted using DAPI counter stain | ratio |
PF2_RER | Relative enrichment ratios (RER) of fungi over prokaryotes on the 30 micrometer pore-size filters versus 0.2 micrometer pore-size filters; mathematically: NEN on the 30 micron filter divided by the NEN on the 0.2 micron filters for fungi | ratio |
Dataset-specific Instrument Name | |
Generic Instrument Name | Fluorescence Microscope |
Dataset-specific Description | Olympus BX51 epifluorescence microscope, U-LH100HG APO mercury burner, 100 x UPlanSApo objective lens, and 20 x ocular magnification. |
Generic Instrument Description | Instruments that generate enlarged images of samples using the phenomena of fluorescence and phosphorescence instead of, or in addition to, reflection and absorption of visible light. Includes conventional and inverted instruments. |
Dataset-specific Instrument Name | |
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. |
Website | |
Platform | R/V Pelagia |
Start Date | 2012-06-23 |
End Date | 2012-07-23 |
Description | Cruise for the MEDEA II project |
Description from NSF award abstract:
In the microbial realm, one of the three domains of life -- the Eukarya -- has received little attention in deep-sea research. This stands in contrast to the fact that in all known aquatic environments, and measured by the amount of material and energy transferred, the link between prokaryotic and eukaryotic cells is one of the most significant trophic interactions on Earth. In terms of volume, the deep sea is the largest biome, and despite its tremendous role in long-term biogeochemical cycles, it has largely been neglected. Biological activity in the deep sea is neither negligible nor homogeneous in space and time. Recent data suggest that biological activity in the dark ocean (as evidenced by respiration rates, bacterial secondary production and a variety of other metrics) is much higher than anticipated from all known organic carbon fuel sources combined (i.e., POC flux, DOC convection, in situ production and active transport by zooplankton). Water masses in the deep ocean represent highly-diverse biogeographic regions with distinct communities and particle distributions. Moreover, because of feeding thresholds, cold temperatures, extreme pressures and unique adaptations that deep-sea microbes exhibit, biological activity rules cannot simply be extrapolated from laboratory cultures and from experiments with surface-dwelling microbes. This study focuses on the fundamental role of eukaryotic microbial communities in deep-sea ecology with the overarching hypothesis that protists represent sensitive biological indicators of utilizable organic carbon. There is good reason to believe that microbial eukaryotes and their activities are better indicators of "new" sources of organic carbon than particle inventories, sediment traps, isotope ratios, or models based on surface production and theoretical flux attenuation. For these new biological indicators to work, however, one needs to separate live from the moribund and dead cells, the bacterivores from saprotrophs, the inactive resting stages from those actively feeding on prokaryotes, the gametes and zoospores from vegetative and feeding stages, and those located on particles from the ones freely suspended in the water column. Each of these groups represents different levels of per-cell energy and carbon requirements.
This study determines the ecological role of eukaryotic microbes in the deep North Atlantic over large geographic regions. The research incorporates two fundamentally different experimental designs that capitalize on different time scales: 1) Short-term incubations (~72 hours) of respiratory activity and bacterivory combined with a high resolution sampling of abundances across large geographic regions performed from a research vessel, and 2) Long-term incubations (=/> 4 weeks) measuring colonization of sinking particles and growth of eukaryotic microbes using free-falling (untethered) vehicles representing the first attempt of physiological rate measurements directly in the deep sea. Methods include new tracers for bacterivory, incubations for single-cell respiration, taxonomic identification using fluorescence in situ hybridization, single-cell genomics, and the first of its kind deep-sea holographic microscope capturing images to a maximum depth of 6000 m at 5 micrometer resolution.
Funding Source | Award |
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NSF Division of Ocean Sciences (NSF OCE) |