BCO-DMO ERDDAP
Accessing BCO-DMO data |
log in
Brought to you by BCO-DMO |
Grid DAP Data | Sub- set | Table DAP Data | Make A Graph | W M S | Source Data Files | Acces- sible | Title | Sum- mary | FGDC, ISO, Metadata | Back- ground Info | RSS | E | Institution | Dataset ID |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
data | graph | files | public | [Light stress grazing: prey and predator exposure] - Prey and predator exposure results from light stress in phytoplankton and dinoflagellate grazing response experiments from August to September of 2018 (Environmental stress and signaling based on reactive oxygen species among planktonic protists) | I M | background | BCO-DMO | bcodmo_dataset_779050 |
Row Type | Variable Name | Attribute Name | Data Type | Value |
---|---|---|---|---|
attribute | NC_GLOBAL | access_formats | String | .htmlTable,.csv,.json,.mat,.nc,.tsv |
attribute | NC_GLOBAL | acquisition_description | String | Phytoplankton light stress \u2013 dinoflagellate grazing experiments General information Emiliania huxleyi strains were grown in f/50 without added Si, except for CCMP1516 which was grown in f/2 for experiments D and I and in f/50 otherwise. All other phytoplankton were grown in f/2 medium without added Si. Most strains (designated CCMP) were obtained from the National Center for Marine Algae and Microbiota except Heterocapsa rotundata, which was from the Norwegian Culture Collection of Algae (NORCCA). Heterotrophic dinoflagellates Amphidinium longum and Oxyrrhis marina were isolated from marine waters of the Salish Sea, grown in ciliate medium (Gifford 1985), and maintained on a mixture of phytoflagellate species. All cultures of any type were grown at a salinity of 30 and a temperature of 15\u00b0C. Phytoplankton were grown at a range of low to moderate irradiances, depending on experiment on a 12L:12D cycle. Heterotrophic dinoflagellates were grown at 10-20 \u00b5mol photons m-2 s-1 on a 12L:12D cycle. Before use in experiments, dinoflagellate predators were fed only Rhodomonas sp. 755 (A. longum) or Dunaliella tertiolecta (O. marina) and allowed to consume these prey until they were nearly gone from the culture. Cells were exposed to experimental light treatments outdoors in a shallow tank filled with flowing seawater supplied from nearby coastal waters. Temperature during experiments was monitored at regular intervals with a thermometer mounted in an unscreened incubation bottle, and ranged from 14-15\u00b0C except for Exp. A, where it averaged 17\u00b0C. Light (incident photosynthetically active radiation, or PAR) was measured with a Li-Cor 2\u03c0 sensor, and logged at 5-min intervals so that total experiment light dose (mol photons m-2) could be computed for specific incubation periods. Control treatments were incubated in 60-ml polycarbonate bottles screened with sufficient neutral density screening to approximate growth irradiances. Higher light exposures were achieved using fewer (or no) layers of neutral density screening, depending on experiment. Except for Exp. E, which used polycarbonate bottles only, all high light treatments used 60-ml Teflon bottles, which are transparent to UV wavelengths. In some experiments high light treatments included both Teflon (UV-transparent) and polycarbonate (UV- opaque) bottles, to isolate the effects of UV on protist responses. Bottles were incubated at ~10 cm depth in the outdoor tank. Experiments A-F exposed only the phytoplankton prey to the light stress treatments (\u2018Single_factor_grazing (prey-only)\u2019 data set [https://www.bco-dmo.org/dataset/779043](\\"https://www.bco- dmo.org/dataset/779043\\")). Cultures were divided into incubation bottles (n=3-5 depending on experiment) and placed in the outdoor tank for 60-120 min. Photosynthetic efficiency (Fv/Fm) was monitored before cells were taken outside (t=0) and, after gentle mixing, at 30-min intervals during the incubations (\u2018FvFm\u2019 data set [https://www.bco- dmo.org/dataset/779033](\\"https://www.bco-dmo.org/dataset/779033\\")). After outdoor exposure, phytoplankton were returned to the laboratory and a subsample from each replicate was added to a corresponding 30-ml polycarbonate bottle containing heterotrophic dinoflagellate predator A. longum to initiate predation experiments. The remainder of the phytoplankton culture volume was placed in an incubator at the culture growth irradiance level, and Fv/Fm monitored at regular intervals during this recovery period. Prey concentrations for predation experiments ranged from 5.0 x 103 cells ml-1 for dinoflagellate Heterocapsa rotundata to 5.0 x 104 cells ml-1 for the various E. huxleyi strains. Prey biomass densities were equivalent for all prey types, at ~500 \u00b5g C liter-1. Carbon per cell for each phytoplankton species was estimated from measured cell volumes and published C:volume conversion factors (Menden-Deuer & Lessard 2000). A. longum concentrations were ~1-2 x 103 cells ml-1, and O. marina concentration (Exp. I only, see below) was 260 cells ml-1. For \u2018prey only exposure\u2019 experiments, predation tests were conducted for 50 min in a laboratory incubator at 15\u00b0C and ~50 \u00b5mol photons m-2 s-1. For \u2018prey and predator exposure\u2019 experiments, predation tests were conducted for 40-60 min under either control or high light outdoor illumination conditions. Predation tests were terminated by adding cells to cold 10% glutaraldehyde and DAPI stain (final concentrations 0.5% and 0.1 \u00b5g ml-1, respectively). After fixation overnight in 4\u00b0C and darkness, samples were filtered (3 or 5 \u00b5m pore-size polycarbonate filters), mounted on slides, and frozen for later examination by epifluorescence microscopy. UV excitation was used to locate and identify dinoflagellate predators from the DAPI-induced fluorescence of their nuclei. Ingested prey were detected using blue light excitation, from the orange (cryptophyte) or red (all other prey) autofluorescence of the prey pigments inside the predator food vacuoles Because A. longum uses a peduncle to feed on cryptophytes, rather than phagocytizing intact cells, the number of ingested prey per predator cannot be quantified for this predator \u2013 prey combination. Therefore for all predator and prey types, each micrograzer cell was scored as \u2018feeding\u2019 or \u2018not feeding\u2019. At least 250 micrograzers per slide were scored; predation intensity was calculated as fraction of the population feeding (= # micrograzers with ingested prey / total # micrograzers scored). Experiments G, H, and I used a matrix design in which predators and prey were exposed to experimental irradiances separately, then combined in various ways and predation measured in outdoor irradiance conditions (\u2018Prey and predator exposure\u2019 data set [https://www.bco- dmo.org/dataset/779050](\\"https://www.bco-dmo.org/dataset/779050\\")). Cultures of predators and prey were incubated in separate bottles for the first 1-1.2 h of exposure time. After that, appropriate volumes of prey with various exposure histories were introduced into predator bottles with various exposure histories, and those predation tests incubated for an additional 40-60 min at the original predator irradiance level. Fv/Fm was monitored throughout (\u2018Photosynthetic efficiency\u2019 data set [https://www.bco- dmo.org/dataset/779033](\\"https://www.bco-dmo.org/dataset/779033\\")), first in the original phytoplankton-only bottles and then in the remaining phytoplankton volume after predation tests were initiated, and finally through a recovery period in the laboratory as described above. At the end of the predation test period, samples were fixed and slides prepared as described above. For more information see Strom et al. (2020). |
attribute | NC_GLOBAL | awards_0_award_nid | String | 614837 |
attribute | NC_GLOBAL | awards_0_award_number | String | OCE-1434842 |
attribute | NC_GLOBAL | awards_0_data_url | String | http://www.nsf.gov/awardsearch/showAward.do?AwardNumber=1434842 |
attribute | NC_GLOBAL | awards_0_funder_name | String | NSF Division of Ocean Sciences |
attribute | NC_GLOBAL | awards_0_funding_acronym | String | NSF OCE |
attribute | NC_GLOBAL | awards_0_funding_source_nid | String | 355 |
attribute | NC_GLOBAL | awards_0_program_manager | String | David L. Garrison |
attribute | NC_GLOBAL | awards_0_program_manager_nid | String | 50534 |
attribute | NC_GLOBAL | cdm_data_type | String | Other |
attribute | NC_GLOBAL | comment | String | Prey and predator exposure results from light stress PI: Suzanne Strom Data Version 1: 2019-10-15 |
attribute | NC_GLOBAL | Conventions | String | COARDS, CF-1.6, ACDD-1.3 |
attribute | NC_GLOBAL | creator_email | String | info at bco-dmo.org |
attribute | NC_GLOBAL | creator_name | String | BCO-DMO |
attribute | NC_GLOBAL | creator_type | String | institution |
attribute | NC_GLOBAL | creator_url | String | https://www.bco-dmo.org/ |
attribute | NC_GLOBAL | data_source | String | extract_data_as_tsv version 2.3 19 Dec 2019 |
attribute | NC_GLOBAL | date_created | String | 2019-10-11T16:13:19Z |
attribute | NC_GLOBAL | date_modified | String | 2020-03-19T20:25:50Z |
attribute | NC_GLOBAL | defaultDataQuery | String | &time<now |
attribute | NC_GLOBAL | doi | String | 10.26008/1912/bco-dmo.779050.1 |
attribute | NC_GLOBAL | infoUrl | String | https://www.bco-dmo.org/dataset/779050 |
attribute | NC_GLOBAL | institution | String | BCO-DMO |
attribute | NC_GLOBAL | instruments_0_acronym | String | LI-COR Biospherical PAR |
attribute | NC_GLOBAL | instruments_0_dataset_instrument_description | String | Irradiance measurements: Li-Cor 1400 data logger with 2-pi (cosine) photosynthetically active radiation (PAR) sensor |
attribute | NC_GLOBAL | instruments_0_dataset_instrument_nid | String | 779056 |
attribute | NC_GLOBAL | instruments_0_description | String | The LI-COR Biospherical PAR Sensor is used to measure Photosynthetically Available Radiation (PAR) in the water column. This instrument designation is used when specific make and model are not known. |
attribute | NC_GLOBAL | instruments_0_instrument_external_identifier | String | https://vocab.nerc.ac.uk/collection/L22/current/TOOL0074/ |
attribute | NC_GLOBAL | instruments_0_instrument_name | String | LI-COR Biospherical PAR Sensor |
attribute | NC_GLOBAL | instruments_0_instrument_nid | String | 480 |
attribute | NC_GLOBAL | instruments_0_supplied_name | String | Li-Cor 1400 data logger with 2-pi (cosine) photosynthetically active radiation (PAR) sensor |
attribute | NC_GLOBAL | instruments_1_acronym | String | Fluorometer |
attribute | NC_GLOBAL | instruments_1_dataset_instrument_description | String | Photosynthetic efficiency measurements: Pulse-Amplitude Modulated Fluorometer: Walz Water PAM |
attribute | NC_GLOBAL | instruments_1_dataset_instrument_nid | String | 779055 |
attribute | NC_GLOBAL | instruments_1_description | String | 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. |
attribute | NC_GLOBAL | instruments_1_instrument_external_identifier | String | https://vocab.nerc.ac.uk/collection/L05/current/113/ |
attribute | NC_GLOBAL | instruments_1_instrument_name | String | Fluorometer |
attribute | NC_GLOBAL | instruments_1_instrument_nid | String | 484 |
attribute | NC_GLOBAL | instruments_1_supplied_name | String | Pulse-Amplitude Modulated Fluorometer: Walz Water PAM |
attribute | NC_GLOBAL | keywords | String | available, bco, bco-dmo, biological, bottle, chemical, combined, Combined_PAR_dose, data, dataset, date, dmo, dose, erddap, experiment, Experiment_ID, feeding, fraction, Fraction_Feeding, management, micrograzer, Micrograzer_Bottle_Type, Micrograzer_PAR_Dose, Micrograzer_Species, num, Num_Micrograzer_Screens, Num_Phytoplankton_Screens, number, oceanography, office, par, photosynthetically, phytoplankton, Phytoplankton_Bottle_Type, Phytoplankton_PAR_dose, Phytoplankton_Species, preliminary, radiation, replicate, Replicate_Number, screens, species, time, type |
attribute | NC_GLOBAL | license | String | https://www.bco-dmo.org/dataset/779050/license |
attribute | NC_GLOBAL | metadata_source | String | https://www.bco-dmo.org/api/dataset/779050 |
attribute | NC_GLOBAL | param_mapping | String | {'779050': {}} |
attribute | NC_GLOBAL | parameter_source | String | https://www.bco-dmo.org/mapserver/dataset/779050/parameters |
attribute | NC_GLOBAL | people_0_affiliation | String | University of Washington |
attribute | NC_GLOBAL | people_0_affiliation_acronym | String | UW |
attribute | NC_GLOBAL | people_0_person_name | String | Suzanne Strom |
attribute | NC_GLOBAL | people_0_person_nid | String | 50471 |
attribute | NC_GLOBAL | people_0_role | String | Principal Investigator |
attribute | NC_GLOBAL | people_0_role_type | String | originator |
attribute | NC_GLOBAL | people_1_affiliation | String | Woods Hole Oceanographic Institution |
attribute | NC_GLOBAL | people_1_affiliation_acronym | String | WHOI BCO-DMO |
attribute | NC_GLOBAL | people_1_person_name | String | Amber York |
attribute | NC_GLOBAL | people_1_person_nid | String | 643627 |
attribute | NC_GLOBAL | people_1_role | String | BCO-DMO Data Manager |
attribute | NC_GLOBAL | people_1_role_type | String | related |
attribute | NC_GLOBAL | project | String | Protist signaling |
attribute | NC_GLOBAL | projects_0_acronym | String | Protist signaling |
attribute | NC_GLOBAL | projects_0_description | String | Description from NSF proposal: This proposal arises from the central premise that the oxidative stress response is an emergent property of phototrophic cellular systems, with implications for nearly every aspect of a phytoplankton cell’s life in the upper ocean. Oxidative stress (OS) arises from the uncompensated production of reactive oxygen species (ROS) within a cell, which can occur in response to a myriad of environmental stressors (e.g. nutrient limitation, temperature extremes, toxins, variable light exposure). In addition to the biochemical damage and physiological impairment that OS can cause, the phytoplankton OS response also includes increased net production and extracellular release of ROS, osmolytes, and other compounds that are known or suspected to be potent signals regulating protist behavior. We hypothesize that, through chemical signaling, oxidative stress acts to govern relationships among environmental variability, phytoplankton condition, and protist predation. Our proposed study of these integrated signaling and response processes has three overarching objectives: 1) Create and characterize oxidatively stressed phytoplankton. We will use light stress (variable exposure to visible light and UV) to create oxidatively stressed phytoplankton in the laboratory. Common coastal taxa with contrasting stress responses will be characterized using an array of fluorescent probes, biochemical measurements, and physiological assays. In addition, intracellular production and extracellular release of ROS and the associated chemical signal DMSP will be quantified. Use of Phaeodactylum tricornutum light stress mutants will add an independent means of connecting OS to signal production and predation response. 2) Examine protist predator responses to oxidatively stressed phytoplankton and associated chemical signals. Responses will be investigated by means of manipulation experiments and thorough characterization of associated signal chemistry. Assessment of predator response will be via predation rate measurements and population aggregation/dispersal behaviors in structured columns. 3) Investigate the prevalence of OS, its environmental correlates, and the microzooplankton predation response in the natural waters of a well-characterized local embayment. Application of ROS probes and OS assays to the natural environment and the design of OS manipulation experiments will be informed by the laboratory experiments using local protist species. Our work will help to elucidate some of the multiple ways in which the OS response can affect phytoplankton fitness, contributing information that can be used to characterize the position of key coastal species along an OS response spectrum. Ultimately such information could be used in trait-based conceptual and numerical models in a manner analogous to cell size and other 'master traits'. Our research will also inform the relatively new and exciting field of chemical signaling in planktonic communities, exploring DMSP- and ROS-based signaling between two of the most significant groups in the plankton, the eukaryotic phytoplankton and their protist predators. Finally, findings will help elucidate the links between environmental stress, phytoplankton response, and predation in planktonic ecosystems. These links relate to central issues in biological oceanography, including the predator-prey interactions that influence bloom demise, and the mechanisms by which protists feed selectively and thereby structure prey communities. The proposed research is a cross-cutting endeavor that unites subjects usually studied in isolation through a novel conceptual framework. Thus the findings have the potential to generate broadly applicable new insights into the ecological and evolutionary regulation of this key trophic link in planktonic food webs. |
attribute | NC_GLOBAL | projects_0_end_date | String | 2017-08 |
attribute | NC_GLOBAL | projects_0_geolocation | String | Salish Sea: 48.5, -122.75 |
attribute | NC_GLOBAL | projects_0_name | String | Environmental stress and signaling based on reactive oxygen species among planktonic protists |
attribute | NC_GLOBAL | projects_0_project_nid | String | 614838 |
attribute | NC_GLOBAL | projects_0_start_date | String | 2014-09 |
attribute | NC_GLOBAL | publisher_name | String | Biological and Chemical Oceanographic Data Management Office (BCO-DMO) |
attribute | NC_GLOBAL | publisher_type | String | institution |
attribute | NC_GLOBAL | sourceUrl | String | (local files) |
attribute | NC_GLOBAL | standard_name_vocabulary | String | CF Standard Name Table v55 |
attribute | NC_GLOBAL | summary | String | Matrix data from light stress in phytoplankton and dinoflagellate grazing response experiments from August of 2016 to September of 2018. Both predators and prey were exposed to experimental irradiances and then tested in an array of combinations. These data were published in Strom et al. (2020). |
attribute | NC_GLOBAL | title | String | [Light stress grazing: prey and predator exposure] - Prey and predator exposure results from light stress in phytoplankton and dinoflagellate grazing response experiments from August to September of 2018 (Environmental stress and signaling based on reactive oxygen species among planktonic protists) |
attribute | NC_GLOBAL | version | String | 1 |
attribute | NC_GLOBAL | xml_source | String | osprey2erddap.update_xml() v1.3 |
variable | Experiment_ID | String | ||
attribute | Experiment_ID | bcodmo_name | String | exp_id |
attribute | Experiment_ID | description | String | Shows letter (A-I) corresponding to experiment ID system used in Strom et al. (submitted), followed by experiment ID used in Strom lab. |
attribute | Experiment_ID | long_name | String | Experiment ID |
attribute | Experiment_ID | units | String | unitless |
variable | Experiment_Date | String | ||
attribute | Experiment_Date | bcodmo_name | String | date |
attribute | Experiment_Date | description | String | Calendar date on which experiment was conducted ISO 8601 Date format yyyy-mm-dd |
attribute | Experiment_Date | long_name | String | Experiment Date |
attribute | Experiment_Date | nerc_identifier | String | https://vocab.nerc.ac.uk/collection/P01/current/ADATAA01/ |
attribute | Experiment_Date | source_name | String | Experiment_Date |
attribute | Experiment_Date | time_precision | String | 1970-01-01 |
attribute | Experiment_Date | units | String | unitless |
variable | Phytoplankton_Species | String | ||
attribute | Phytoplankton_Species | bcodmo_name | String | animal_group |
attribute | Phytoplankton_Species | description | String | Shows species and strain number (CCMP), where available, for phytoplankton used in light stress experiments (H. rotundata strain number refers to SCCAP culture collection). See species list (supplemental document) for species codes and the corresponding species names. |
attribute | Phytoplankton_Species | long_name | String | Phytoplankton Species |
attribute | Phytoplankton_Species | units | String | unitless |
variable | Micrograzer_Species | String | ||
attribute | Micrograzer_Species | bcodmo_name | String | animal_group |
attribute | Micrograzer_Species | description | String | Shows species and strain number (CCMP), where available, for micrograzers used in light stress experiments |
attribute | Micrograzer_Species | long_name | String | Micrograzer Species |
attribute | Micrograzer_Species | units | String | unitless |
variable | Phytoplankton_Bottle_Type | String | ||
attribute | Phytoplankton_Bottle_Type | bcodmo_name | String | bottle |
attribute | Phytoplankton_Bottle_Type | description | String | Incubation bottle material for phytoplankton during first phase of experiment, when phytoplankton and grazers were exposed separately; PC = polycarbonate; Tef = Teflon |
attribute | Phytoplankton_Bottle_Type | long_name | String | Phytoplankton Bottle Type |
attribute | Phytoplankton_Bottle_Type | units | String | unitless |
variable | Num_Phytoplankton_Screens | byte | ||
attribute | Num_Phytoplankton_Screens | _FillValue | byte | 127 |
attribute | Num_Phytoplankton_Screens | actual_range | byte | 0, 7 |
attribute | Num_Phytoplankton_Screens | bcodmo_name | String | sample_descrip |
attribute | Num_Phytoplankton_Screens | description | String | Number of neutral density screen layers used to shade incubation bottles containing phytoplankton during first phase of experiment |
attribute | Num_Phytoplankton_Screens | long_name | String | Num Phytoplankton Screens |
attribute | Num_Phytoplankton_Screens | units | String | unitless |
variable | Phytoplankton_PAR_dose | float | ||
attribute | Phytoplankton_PAR_dose | _FillValue | float | NaN |
attribute | Phytoplankton_PAR_dose | actual_range | float | 0.04, 4.81 |
attribute | Phytoplankton_PAR_dose | bcodmo_name | String | PAR |
attribute | Phytoplankton_PAR_dose | description | String | Total dose of photosynthetically active radiation received by phytoplankton during first phase of outdoor ‘light stress’ incubation period |
attribute | Phytoplankton_PAR_dose | long_name | String | Phytoplankton PAR Dose |
attribute | Phytoplankton_PAR_dose | units | String | mol photons m-2 |
variable | Micrograzer_Bottle_Type | String | ||
attribute | Micrograzer_Bottle_Type | bcodmo_name | String | bottle |
attribute | Micrograzer_Bottle_Type | description | String | Incubation bottle material for micrograzers (predators) during both first phase of experiment, when phytoplankton and grazers were exposed separately, as well as during second phase, when prey and predators were combined; PC = polycarbonate; Tef = Teflon |
attribute | Micrograzer_Bottle_Type | long_name | String | Micrograzer Bottle Type |
attribute | Micrograzer_Bottle_Type | units | String | unitless |
variable | Num_Micrograzer_Screens | byte | ||
attribute | Num_Micrograzer_Screens | _FillValue | byte | 127 |
attribute | Num_Micrograzer_Screens | actual_range | byte | 0, 7 |
attribute | Num_Micrograzer_Screens | bcodmo_name | String | sample_descrip |
attribute | Num_Micrograzer_Screens | description | String | Number of neutral density screen layers used to wrap bottles during initial exposure phase. Micrograzer exposure conditions. |
attribute | Num_Micrograzer_Screens | long_name | String | Num Micrograzer Screens |
attribute | Num_Micrograzer_Screens | units | String | unitless |
variable | Micrograzer_PAR_Dose | float | ||
attribute | Micrograzer_PAR_Dose | _FillValue | float | NaN |
attribute | Micrograzer_PAR_Dose | actual_range | float | 0.04, 4.81 |
attribute | Micrograzer_PAR_Dose | bcodmo_name | String | PAR |
attribute | Micrograzer_PAR_Dose | description | String | Total dose of photosynthetically active radiation received by micrograzers during first phase of outdoor ‘light stress’ incubation period, when phytoplankton and micrograzers were exposed separately |
attribute | Micrograzer_PAR_Dose | long_name | String | Micrograzer PAR Dose |
attribute | Micrograzer_PAR_Dose | units | String | mol photons m-2 |
variable | Combined_PAR_dose | float | ||
attribute | Combined_PAR_dose | _FillValue | float | NaN |
attribute | Combined_PAR_dose | actual_range | float | 0.04, 3.3 |
attribute | Combined_PAR_dose | bcodmo_name | String | PAR |
attribute | Combined_PAR_dose | description | String | Total dose of photosynthetically active radiation received by micrograzers plus phytoplankton during second phase of experiment when prey and predators were combined |
attribute | Combined_PAR_dose | long_name | String | Combined PAR Dose |
attribute | Combined_PAR_dose | units | String | mol photons m-2 |
variable | Replicate_Number | byte | ||
attribute | Replicate_Number | _FillValue | byte | 127 |
attribute | Replicate_Number | actual_range | byte | 1, 6 |
attribute | Replicate_Number | bcodmo_name | String | replicate |
attribute | Replicate_Number | colorBarMaximum | double | 100.0 |
attribute | Replicate_Number | colorBarMinimum | double | 0.0 |
attribute | Replicate_Number | description | String | Identifies an individual replicate bottle |
attribute | Replicate_Number | long_name | String | Replicate Number |
attribute | Replicate_Number | units | String | unitless |
variable | Fraction_Feeding | float | ||
attribute | Fraction_Feeding | _FillValue | float | NaN |
attribute | Fraction_Feeding | actual_range | float | 0.13, 0.81 |
attribute | Fraction_Feeding | bcodmo_name | String | unknown |
attribute | Fraction_Feeding | colorBarMaximum | double | 1.0 |
attribute | Fraction_Feeding | colorBarMinimum | double | 0.0 |
attribute | Fraction_Feeding | description | String | Fraction of the total enumerated micrograzer population that contained ingested phytoplankton prey after the 40-60 min predation test period under outdoor illumination conditions. |
attribute | Fraction_Feeding | long_name | String | Fraction Feeding |
attribute | Fraction_Feeding | units | String | dimensionless |
The information in the table above is also available in other file formats (.csv, .htmlTable, .itx, .json, .jsonlCSV1, .jsonlCSV, .jsonlKVP, .mat, .nc, .nccsv, .tsv, .xhtml) via a RESTful web service.