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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 |
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data | graph | files | public | [MO - virioplankton abundance] - Virioplankton abundance from multiple cruises at the Bermuda AtlanticTime Series Station (BATS), Western Sargasso Sea from 2000-2011 (Ocean Microbial Observatory project) (Transitions in the Surface Layer and the Role of Vertically Stratified Microbial Communities in the Carbon Cycle - An Oceanic Microbial Observatory) | F I M | background | BCO-DMO | bcodmo_dataset_543808 |
Row Type | Variable Name | Attribute Name | Data Type | Value |
---|---|---|---|---|
attribute | NC_GLOBAL | access_formats | String | .htmlTable,.csv,.json,.mat,.nc,.tsv,.esriCsv,.geoJson |
attribute | NC_GLOBAL | acquisition_description | String | Methodology:\u00a0from\u00a0Parsons et al (2011): Study site and sample collection: Samples were collected aboard the\u00a0RV Weatherbird II\u00a0or the\u00a0RV Atlantic Explorer\u00a0at the BATS site (31\u00b0 40\u2032 N, 64\u00b010\u2032 W). All cruises were conducted as part of the larger BATS program and sampled at least monthly with biweekly sampling between February and April. This sampling strategy has been successful in revealing the major temporal microbial and biogeochemical patterns at this site (Carlson and Ducklow, 1996;\u00a0Steinberg et al., 2001;\u00a0Morris et al., 2005;\u00a0Carlson et al., 2009;\u00a0Treusch et al., 2009;\u00a0Lomas et al., 2010). A broader assessment of the BATS biogeochemical data is presented in\u00a0Deep Sea Research II\u00a0in 1996 (volume 43, issues 2\u20133) and 2001 (volume 48, issues 8\u20139). Samples for virioplankton (0, 20, 40, 60, 80, 100, 140, 160, 200, 250 and 300\u2009m) and bacterioplankton (0, 10, 20, 40, 60, 80, 100, 120, 140, 160, 200, 250 and 300\u2009m) were collected at the BATS site from January 2000 to December 2009 via conductivity, temperature, depth profiling rosette equipped with 12\u2009l Niskin bottles. The 120\u2009m virioplankton sample was added after October 2007. Throughout the entire time-series, all virioplankton samples were fixed with 0.02\u2009um filtered formalin (1% final concentration), placed in 5\u2009ml cryovials and flash frozen in liquid nitrogen (Wen et al., 2004) until processing (within 12 weeks of collection). Samples for bacterioplankton abundance were fixed with 0.2\u2009um filtered gluteraldehyde (1% final concentration) and stored at either 4\u2009\u00b0C for 72\u2009h or flash frozen and subsequently stored at \u221280\u2009\u00b0C for up to 6 months until processing as described in\u00a0Steinberg et al (2001). Storage tests demonstrated no appreciable loss of virioplankton or bacterioplankton abundance when stored in liquid nitrogen for periods up to 6 months (unpublished data). Picophytoplankton samples were collected at the same depths through 250\u2009m from October 2001 to December 2009 (Casey et al., 2007). Samples for fluorescence\u00a0in situ\u00a0hybridization (FISH) of specific heterotrophic bacterioplankton lineages were collected from the upper 300\u2009m from January 2003 to December 2005 (Carlson et al., 2009). Biogeochemical and physical data collected at the BATS site are available at\u00a0[http://bats.bios.edu](\\"http://bats.bios.edu\\"). The MLD was determined as the depth where potential density (sigma-t) of the water was equal to sea surface sigma-t\u00a0plus the equivalent in sigma-t\u00a0to a 0.2\u2009\u00b0C decrease in temperature (Sprintall and Tomczak, 1992). Contour plots were created in Ocean Data View (R Schlitzer,\u00a0[https://odv.awi.de/](\\"https://odv.awi.de/\\")) with VG Gridding and linear mapping adjusted to the median of each data set. Statistics (Pearson's correlation and two-tailed Student's\u00a0t-test for unequal variances), ratios and percent contributions were determined using Microsoft Excel. Virioplankton abundance: Virioplankton abundance was enumerated according to the methods of\u00a0Noble and Fuhrman (1998). Briefly, water samples were filtered on to 0.02\u2009um Anodisc aluminum oxide filters (Whatman, Kent, UK), stained with SYBR Green I (Molecular Probes Inc., Eugene, OR, USA), and enumerated via epifluorescence microscopy using an Olympus AX70 microscope (Olympus, Tokyo, Japan) equipped with a Toshiba CCD video camera (Irvine, CA, USA) and Pro- series Capture Kit version 4.5 (I-CUBE, Crofton, MD, USA). Ten images from each sample were processed with scripts written in Image Pro Plus (Media Cybernetics, Bethesda, MD, USA) for particles sized 0.01\u20130.27\u2009um2, using the clean borders function (cells touching the edge of the image or grid were omitted). We consider these estimates of viral abundance conservative because it is possible that some viral particles less than one pixel were omitted from the final count. We performed pairwise comparisons of automated versus manual enumeration of virioplankton abundance to determine any discrepancies between the two approaches. Samples collected along a gradient from offshore (BATS;\u00a0n=92) to onshore waters of Bermuda (n=32) were highly correlated with automated counts being slightly greater than manual counts (slope=1.07,\u00a0r=0.99,\u00a0n=134). The lower estimates of viral abundance from manual counts may have resulted from image fading during enumeration and/or operator fatigue. We argue that for this study, the automated image analysis was the most reliable approach for viral particle enumeration. The coefficient of variation for the automated counts averaged 11% (n=1517). |
attribute | NC_GLOBAL | awards_0_award_nid | String | 514363 |
attribute | NC_GLOBAL | awards_0_award_number | String | OCE-0802004 |
attribute | NC_GLOBAL | awards_0_data_url | String | http://www.nsf.gov/awardsearch/showAward?AWD_ID=0802004 |
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 | Virioplankton abundance at BATS site, 2000-2011 C. Carlson (UC-SB) version: 2020-05-04 |
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 | dataset_current_state | String | Final and no updates |
attribute | NC_GLOBAL | date_created | String | 2014-12-23T18:13:37Z |
attribute | NC_GLOBAL | date_modified | String | 2020-05-11T19:09:23Z |
attribute | NC_GLOBAL | defaultDataQuery | String | &time<now |
attribute | NC_GLOBAL | doi | String | 10.26008/1912/bco-dmo.543808.1 |
attribute | NC_GLOBAL | Easternmost_Easting | double | -63.988 |
attribute | NC_GLOBAL | geospatial_lat_max | double | 31.81 |
attribute | NC_GLOBAL | geospatial_lat_min | double | 31.352 |
attribute | NC_GLOBAL | geospatial_lat_units | String | degrees_north |
attribute | NC_GLOBAL | geospatial_lon_max | double | -63.988 |
attribute | NC_GLOBAL | geospatial_lon_min | double | -64.312 |
attribute | NC_GLOBAL | geospatial_lon_units | String | degrees_east |
attribute | NC_GLOBAL | geospatial_vertical_max | double | 502.375 |
attribute | NC_GLOBAL | geospatial_vertical_min | double | 0.9 |
attribute | NC_GLOBAL | geospatial_vertical_positive | String | down |
attribute | NC_GLOBAL | geospatial_vertical_units | String | m |
attribute | NC_GLOBAL | infoUrl | String | https://www.bco-dmo.org/dataset/543808 |
attribute | NC_GLOBAL | institution | String | BCO-DMO |
attribute | NC_GLOBAL | instruments_0_acronym | String | Niskin bottle |
attribute | NC_GLOBAL | instruments_0_dataset_instrument_description | String | 12 liter Niskin bottles |
attribute | NC_GLOBAL | instruments_0_dataset_instrument_nid | String | 543815 |
attribute | NC_GLOBAL | instruments_0_description | String | 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. |
attribute | NC_GLOBAL | instruments_0_instrument_external_identifier | String | https://vocab.nerc.ac.uk/collection/L22/current/TOOL0412/ |
attribute | NC_GLOBAL | instruments_0_instrument_name | String | Niskin bottle |
attribute | NC_GLOBAL | instruments_0_instrument_nid | String | 413 |
attribute | NC_GLOBAL | instruments_0_supplied_name | String | Niskin bottle |
attribute | NC_GLOBAL | instruments_1_acronym | String | CTD |
attribute | NC_GLOBAL | instruments_1_dataset_instrument_nid | String | 543816 |
attribute | NC_GLOBAL | instruments_1_description | String | The Conductivity, Temperature, Depth (CTD) unit is an integrated instrument package designed to measure the conductivity, temperature, and pressure (depth) of the water column. The instrument is lowered via cable through the water column and permits scientists observe the physical properties in real time via a conducting cable connecting the CTD to a deck unit and computer on the ship. The CTD is often configured with additional optional sensors including fluorometers, transmissometers and/or radiometers. It is often combined with a Rosette of water sampling bottles (e.g. Niskin, GO-FLO) for collecting discrete water samples during the cast. This instrument designation is used when specific make and model are not known. |
attribute | NC_GLOBAL | instruments_1_instrument_external_identifier | String | https://vocab.nerc.ac.uk/collection/L05/current/130/ |
attribute | NC_GLOBAL | instruments_1_instrument_name | String | CTD profiler |
attribute | NC_GLOBAL | instruments_1_instrument_nid | String | 417 |
attribute | NC_GLOBAL | instruments_1_supplied_name | String | CTD |
attribute | NC_GLOBAL | instruments_2_acronym | String | Fluorescence Microscope |
attribute | NC_GLOBAL | instruments_2_dataset_instrument_description | String | Olympus AX70 microscope (Olympus, Tokyo, Japan) equipped with a Toshiba CCD video camera (Irvine, CA, USA) |
attribute | NC_GLOBAL | instruments_2_dataset_instrument_nid | String | 543818 |
attribute | NC_GLOBAL | instruments_2_description | String | A Fluorescence (or Epifluorescence) Microscope Image Analysis System uses semi-automated color image analysis to determine cell abundance, dimensions and biovolumes from an Epifluorescence Microscope. An Epifluorescence Microscope (conventional and inverted) includes a camera system that generates enlarged images of prepared samples. The microscope uses excitation ultraviolet light and the phenomena of fluorescence and phosphorescence instead of, or in addition to, reflection and absorption of visible light. |
attribute | NC_GLOBAL | instruments_2_instrument_external_identifier | String | https://vocab.nerc.ac.uk/collection/L05/current/LAB06/ |
attribute | NC_GLOBAL | instruments_2_instrument_name | String | Fluorescence Microscope Image Analysis System |
attribute | NC_GLOBAL | instruments_2_instrument_nid | String | 508 |
attribute | NC_GLOBAL | instruments_2_supplied_name | String | Epifluorescence Microscope |
attribute | NC_GLOBAL | instruments_3_acronym | String | Flow Cytometer |
attribute | NC_GLOBAL | instruments_3_dataset_instrument_description | String | Becton Dickenson (Franklin Lakes, NJ, USA; formerly Cytopeia) high speed jet-in-air InFlux flow cytometer, using a 488 nm blue excitation laser, appropriate Chl-a (692±20 nm) and phycoerythrin (580±15 nm) bandpass filters. |
attribute | NC_GLOBAL | instruments_3_dataset_instrument_nid | String | 543819 |
attribute | NC_GLOBAL | instruments_3_description | String | 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) |
attribute | NC_GLOBAL | instruments_3_instrument_external_identifier | String | https://vocab.nerc.ac.uk/collection/L05/current/LAB37/ |
attribute | NC_GLOBAL | instruments_3_instrument_name | String | Flow Cytometer |
attribute | NC_GLOBAL | instruments_3_instrument_nid | String | 660 |
attribute | NC_GLOBAL | instruments_3_supplied_name | String | Flow Cytometer |
attribute | NC_GLOBAL | keywords | String | abund, abund_vir, abund_vir_sd, bco, bco-dmo, biological, chemical, cruise, cruise_ID, data, dataset, date, date_in, decyear, depth, depth_mixed, depth_nom, dmo, erddap, latitude, longitude, management, oceanography, office, preliminary, station, vir |
attribute | NC_GLOBAL | license | String | https://www.bco-dmo.org/dataset/543808/license |
attribute | NC_GLOBAL | metadata_source | String | https://www.bco-dmo.org/api/dataset/543808 |
attribute | NC_GLOBAL | Northernmost_Northing | double | 31.81 |
attribute | NC_GLOBAL | param_mapping | String | {'543808': {'lat_in': 'master - latitude', 'depth': 'master - depth', 'lon_in': 'master - longitude'}} |
attribute | NC_GLOBAL | parameter_source | String | https://www.bco-dmo.org/mapserver/dataset/543808/parameters |
attribute | NC_GLOBAL | people_0_affiliation | String | University of California-Santa Barbara |
attribute | NC_GLOBAL | people_0_affiliation_acronym | String | UCSB |
attribute | NC_GLOBAL | people_0_person_name | String | Craig Carlson |
attribute | NC_GLOBAL | people_0_person_nid | String | 50575 |
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 | Oregon State University |
attribute | NC_GLOBAL | people_1_affiliation_acronym | String | OSU |
attribute | NC_GLOBAL | people_1_person_name | String | Dr Stephen Giovannoni |
attribute | NC_GLOBAL | people_1_person_nid | String | 514364 |
attribute | NC_GLOBAL | people_1_role | String | Co-Principal Investigator |
attribute | NC_GLOBAL | people_1_role_type | String | originator |
attribute | NC_GLOBAL | people_2_affiliation | String | Woods Hole Oceanographic Institution |
attribute | NC_GLOBAL | people_2_affiliation_acronym | String | WHOI BCO-DMO |
attribute | NC_GLOBAL | people_2_person_name | String | Nancy Copley |
attribute | NC_GLOBAL | people_2_person_nid | String | 50396 |
attribute | NC_GLOBAL | people_2_role | String | BCO-DMO Data Manager |
attribute | NC_GLOBAL | people_2_role_type | String | related |
attribute | NC_GLOBAL | project | String | Ocean Microbial Observatory |
attribute | NC_GLOBAL | projects_0_acronym | String | Ocean Microbial Observatory |
attribute | NC_GLOBAL | projects_0_description | String | (Adapted from the NSF award abstract) The premise of this project is that stratified bacterioplankton clades engage in specialized biogeochemical activities that can be identified by integrated oceanographic and microbiological approaches. Specifically, the objective of this project is to assess if the mesopelagic microbial community rely on diagenetically altered organic matter and subcellular fragments that are produced by microbial processes in the euphotic zone and delivered into the upper mesopelagic by sinking or mixing. In past efforts this microbial observatory had greater success cultivating members of the euphotic zone microbial community, and revealed an unanticipated growth requirement for reduced sulfur compounds in alphaproteobacteria of the SAR11 clade. Genomic information showed that intense competition for substrates imposes trade-offs on bacterioplankton - there are regions of N dimensional nutrient space where specialists win. We postulate that specific growth requirements may explain some the regular spatial and temporal patterns that have been observed in upper mesopelagic bacterioplankton communities, and the difficulties of culturing some of these organisms. The specific objectives of this project are: 1) to produce 13C and 15N labeled subcellular (e.g., soluble, cell wall, and membrane) and DOM fractions from photosynthetic plankton cultures and use stable isotope probing to identify specific clades in the surface and upper mesopelagic microbial community that assimilate fractions of varying composition and lability. 2) to use fluorescence in situ hybridization approaches to monitor temporal and spatial variability of specific microbial populations identified from the SIP and HTC experiments. To increase resolution we will use CARD-FISH protocols. 3) to measure the proteomes of bacterioplankton communities to identify highly translated genes in the surface layer and upper mesopelagic, and community responses to seasonal nutrient limitation. 4) and, to cultivate these organisms via high throughput culturing (HTC) by pursuing the hypothesis that they require specific nutrient factors and/or diagenetically altered organic substrates. Complete genome sequences from key organisms will be sought and used as queries to study patterns of natural variation in genes and populations that have been associated with biogeochemically important functions. |
attribute | NC_GLOBAL | projects_0_end_date | String | 2014-07 |
attribute | NC_GLOBAL | projects_0_geolocation | String | Bermuda Atlantic Time-Series study site |
attribute | NC_GLOBAL | projects_0_name | String | Transitions in the Surface Layer and the Role of Vertically Stratified Microbial Communities in the Carbon Cycle - An Oceanic Microbial Observatory |
attribute | NC_GLOBAL | projects_0_project_nid | String | 514365 |
attribute | NC_GLOBAL | projects_0_project_website | String | http://www.bios.edu/research/projects/oceanic-microbial-observatory/ |
attribute | NC_GLOBAL | projects_0_start_date | String | 2008-08 |
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 | Southernmost_Northing | double | 31.352 |
attribute | NC_GLOBAL | standard_name_vocabulary | String | CF Standard Name Table v55 |
attribute | NC_GLOBAL | summary | String | Virioplankton abundances were measured from samples collected from January 2000 to December 2011 at the Bermuda Atlantic Time Series Station (BATS), Western Sargasso Sea, as part of the larger BATS program aboard the R/V Weatherbird II or the R/V Atlantic Explorer. Supporting data provided by the BATS time-series program and are available at (http://bats.bios.edu/). |
attribute | NC_GLOBAL | title | String | [MO - virioplankton abundance] - Virioplankton abundance from multiple cruises at the Bermuda AtlanticTime Series Station (BATS), Western Sargasso Sea from 2000-2011 (Ocean Microbial Observatory project) (Transitions in the Surface Layer and the Role of Vertically Stratified Microbial Communities in the Carbon Cycle - An Oceanic Microbial Observatory) |
attribute | NC_GLOBAL | version | String | 1 |
attribute | NC_GLOBAL | Westernmost_Easting | double | -64.312 |
attribute | NC_GLOBAL | xml_source | String | osprey2erddap.update_xml() v1.5 |
variable | station | String | ||
attribute | station | bcodmo_name | String | station |
attribute | station | description | String | BATS cruise number during which sample was collected |
attribute | station | long_name | String | Station |
attribute | station | units | String | unitless |
variable | cruise_ID | int | ||
attribute | cruise_ID | _FillValue | int | 2147483647 |
attribute | cruise_ID | actual_range | int | 101360101, 2026700416 |
attribute | cruise_ID | bcodmo_name | String | cruise_id |
attribute | cruise_ID | description | String | BATS cruise ID for the sample that matches the BATS sample collected from the same niskin |
attribute | cruise_ID | long_name | String | Cruise ID |
attribute | cruise_ID | units | String | unitless |
variable | date_in | String | ||
attribute | date_in | bcodmo_name | String | date |
attribute | date_in | description | String | date of collection at the time of CTD entry year month day |
attribute | date_in | long_name | String | Date In |
attribute | date_in | nerc_identifier | String | https://vocab.nerc.ac.uk/collection/P01/current/ADATAA01/ |
attribute | date_in | units | String | unitless |
variable | decyear | double | ||
attribute | decyear | _FillValue | double | NaN |
attribute | decyear | actual_range | double | 2000.0761, 2011.93973 |
attribute | decyear | bcodmo_name | String | year_decimal |
attribute | decyear | description | String | decimal year |
attribute | decyear | long_name | String | Decyear |
attribute | decyear | units | String | unitless |
variable | latitude | double | ||
attribute | latitude | _CoordinateAxisType | String | Lat |
attribute | latitude | _FillValue | double | NaN |
attribute | latitude | actual_range | double | 31.352, 31.81 |
attribute | latitude | axis | String | Y |
attribute | latitude | bcodmo_name | String | latitude |
attribute | latitude | colorBarMaximum | double | 90.0 |
attribute | latitude | colorBarMinimum | double | -90.0 |
attribute | latitude | description | String | Latitude at the time of CTD entry in degrees N |
attribute | latitude | ioos_category | String | Location |
attribute | latitude | long_name | String | Latitude |
attribute | latitude | nerc_identifier | String | https://vocab.nerc.ac.uk/collection/P09/current/LATX/ |
attribute | latitude | source_name | String | lat_in |
attribute | latitude | standard_name | String | latitude |
attribute | latitude | units | String | degrees_north |
variable | longitude | double | ||
attribute | longitude | _CoordinateAxisType | String | Lon |
attribute | longitude | _FillValue | double | NaN |
attribute | longitude | actual_range | double | -64.312, -63.988 |
attribute | longitude | axis | String | X |
attribute | longitude | bcodmo_name | String | longitude |
attribute | longitude | colorBarMaximum | double | 180.0 |
attribute | longitude | colorBarMinimum | double | -180.0 |
attribute | longitude | description | String | Longitude at the time of CTD entry in degrees W |
attribute | longitude | ioos_category | String | Location |
attribute | longitude | long_name | String | Longitude |
attribute | longitude | nerc_identifier | String | https://vocab.nerc.ac.uk/collection/P09/current/LONX/ |
attribute | longitude | source_name | String | lon_in |
attribute | longitude | standard_name | String | longitude |
attribute | longitude | units | String | degrees_east |
variable | depth | double | ||
attribute | depth | _CoordinateAxisType | String | Height |
attribute | depth | _CoordinateZisPositive | String | down |
attribute | depth | _FillValue | double | NaN |
attribute | depth | actual_range | double | 0.9, 502.375 |
attribute | depth | axis | String | Z |
attribute | depth | bcodmo_name | String | depth |
attribute | depth | colorBarMaximum | double | 8000.0 |
attribute | depth | colorBarMinimum | double | -8000.0 |
attribute | depth | colorBarPalette | String | TopographyDepth |
attribute | depth | description | String | the actual depth in meters |
attribute | depth | ioos_category | String | Location |
attribute | depth | long_name | String | Depth |
attribute | depth | nerc_identifier | String | https://vocab.nerc.ac.uk/collection/P09/current/DEPH/ |
attribute | depth | positive | String | down |
attribute | depth | standard_name | String | depth |
attribute | depth | units | String | m |
variable | depth_nom | short | ||
attribute | depth_nom | _FillValue | short | 32767 |
attribute | depth_nom | actual_range | short | 1, 400 |
attribute | depth_nom | bcodmo_name | String | depth_n |
attribute | depth_nom | colorBarMaximum | double | 8000.0 |
attribute | depth_nom | colorBarMinimum | double | -8000.0 |
attribute | depth_nom | colorBarPalette | String | TopographyDepth |
attribute | depth_nom | description | String | bottle target depths in meters |
attribute | depth_nom | long_name | String | Depth |
attribute | depth_nom | standard_name | String | depth |
attribute | depth_nom | units | String | meters |
variable | depth_mixed | short | ||
attribute | depth_mixed | _FillValue | short | 32767 |
attribute | depth_mixed | actual_range | short | 8, 248 |
attribute | depth_mixed | bcodmo_name | String | depth_mixed_layer |
attribute | depth_mixed | colorBarMaximum | double | 8000.0 |
attribute | depth_mixed | colorBarMinimum | double | -8000.0 |
attribute | depth_mixed | colorBarPalette | String | TopographyDepth |
attribute | depth_mixed | description | String | mixed layer depth in meters; MLD was determined as the depth where potential density (sigma-t) of the water was equal to sea surface sigma-t plus the equivalent in sigma-t to a 0.2 1C decrease in temperature (Sprintall and Tomczak 1992). |
attribute | depth_mixed | long_name | String | Depth |
attribute | depth_mixed | standard_name | String | depth |
attribute | depth_mixed | units | String | meters |
variable | abund_vir | float | ||
attribute | abund_vir | _FillValue | float | NaN |
attribute | abund_vir | actual_range | float | 0.14, 11.703 |
attribute | abund_vir | bcodmo_name | String | cell_concentration |
attribute | abund_vir | description | String | Virioplankton abundance 10^9 cells per liter |
attribute | abund_vir | long_name | String | Abund Vir |
attribute | abund_vir | units | String | 10^9 cells per liter |
variable | abund_vir_sd | float | ||
attribute | abund_vir_sd | _FillValue | float | NaN |
attribute | abund_vir_sd | actual_range | float | 0.014, 5.308 |
attribute | abund_vir_sd | bcodmo_name | String | cell_concentration |
attribute | abund_vir_sd | colorBarMaximum | double | 50.0 |
attribute | abund_vir_sd | colorBarMinimum | double | 0.0 |
attribute | abund_vir_sd | description | String | standard deviation for Virioplankton Abundance in 10^9 cells per liter |
attribute | abund_vir_sd | long_name | String | Abund Vir Sd |
attribute | abund_vir_sd | units | String | 10^9 cells per liter |
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.