BCO-DMO ERDDAP
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Row Type Variable Name Attribute Name Data Type Value
attribute NC_GLOBAL access_formats String .htmlTable,.csv,.json,.mat,.nc,.tsv,.esriCsv,.geoJson,.odvTxt
attribute NC_GLOBAL acquisition_description String Study Site and CTD Casts  \n Data were collected on four cruises in the Sargasso Sea on board the R/V\nAtlantic Explorer. On each cruise, sampling was conducted at three stations:\nthe center and edge of a mesoscale eddy and at one station outside of the\neddy. Eddies were identified using satellite-derived sea level anomaly (SLA)\ndata provided by Dr. Dennis McGillicuddy and Dr. Valery Kosnyrev of the Woods\nHole Oceanographic Institution. Target eddies (one per cruise) were initially\nidentified on the day of departure; the ship's position within the eddy (at\nthe center or the edge, as appropriate) was confirmed by daily checks of SLA\ndata.\n \nAt each station, high resolution CTD casts to ~2000 m were performed at noon\nto measure core physical, chemical and biological parameters of the water\ncolumn. In addition to the core CTD casts, pre-dawn \\\"Productivity\\\" CTD casts\nwere performed to collect water for measurements of size-fractionated biomass\n(as chl a) and size-fractionated primary productivity. Samples were obtained\nusing the 24 bottle Niskin rosette from 3-4 depths (20 m, 40-50 m, deep\nfluorescence maximum (~80 m), and 100 m). Ten-liter polycarbonate collection\nbottles (covered with black tape) were pre-rinsed with sample water and were\nfilled by draining the Niskin bottles through opaque tubing. All samples were\npre-filtered through a 200 um Nitex screen. Further handling of the samples\nwas done in the dark or under red light.\n \nThe 200 um pre-screened water from pre-dawn productivity casts was used for\nmeasurements of size-fractionated biomass (as chl a) and biomarker\nphotopigments by HPLC and for measurements of size-fractionated primary\nproductivity.\\u00a0 HPLC pigments were also used for taxonomic identification\nof total and size-fractionated phytoplankton groups using ChemTax analyses.\nSamples for microscopy were also taken from productivity casts as verification\nof the ChemTax results using methods described above for core CTD casts.\\u00a0\n \nTotal phytoplankton biomass was measured directly by filtering triplicate\naliquots of 1 to 2 liters of pre-screened water onto GF/F filters. This gave\ntotal chl a in the size fraction 0.7 to 200 um. The biomass of three size\nclasses of phytoplankton was quantified by differential filtration: the\npicophytoplankton (0.7-2 um), the nanophytoplankton (2-20 um) and the\nmicrophytoplankton (20-200 um) as follows. Triplicate aliquots of 1 to 2\nliters of pre-screened water were filtered through a 2 um Nuclepore filter\nthen onto a GF/F filter (= picophytoplankton, 0.7-2 um). Triplicate aliquots\nof pre-screened water were also filtered through a 20 um Nitex mesh then onto\na GF/F filter (= 0.7-20 um). Biomass of the nanophytoplankton size class was\ndetermined by subtracting the picophytoplankton biomass from the 0.7-20 um\nbiomass. Microphytoplankton biomass was determined by subtracting the 0.7-20\num biomass from the total chl a value. Filters were folded and placed in 1.5\nml cryotubes and frozen at -80\\u00b0 C until later analysis at the University\nof South Carolina (USC) using the methods below.\\u00a0\n \nPrimary Prodcutivity Measurements  \n For size-fractionated primary productivity measurements, 200 um pre-screened\nwater collected from discrete depths were dispensed into Nalgene polycarbonate\nincubation bottles (7-8 clear bottles plus 1-2 dark bottles per depth;\n800-1200 ml each). Bottles were spiked with 14C-labeled sodium bicarbonate\n(PerkinElmer Health Sciences Inc.) to a final activity 0.04-0.08 uCi ml-1 per\nbottle. An additional bottle per depth was used as a particulate blank (T0)\n(Barber et al., 1996). The T0 bottles were immediately filtered onto a GF/F,\nacidified with 500 ul 0.5 N HCl and left open to fume for 24 hours (Barber et\nal., 1996). Samples for total counts (Tc; 100 ul) were collected from one\nbottle per depth and combined with 200 ul of phenylethylamine (PEA) and 5 ml\nof scintillation cocktail (EcoLume, MPBiomedicals, Solon, Ohio). All bottles\nwere incubated in situ at the depth of collection. Incubations were started\nbefore sunrise (usually between 05:00 and 06:00 h) and were terminated 24 h\nlater. The productivity array was tracked using a Telonics, Inc. transponder\nplatform subscribed to the ARGOS satellite tracking system.\n \nTotal phytoplankton primary productivity was measured directly by filtering\ntriplicate incubation bottles onto GF/F filters. This gave total primary\nproductivity in the size fraction 0.7 to 200 um. Dark bottle productivity was\nalso measured directly by filtering dark bottles directly onto GF/F filters (=\ndark productivity; 0.7-200 um). Size-fractionated rates of primary\nproductivity of the picophytoplankton, nanophytoplankton and\nmicrophytoplankton were made by differential filtration. Two 1 liter bottles\nwere filtered through a 20 um Nitex mesh then onto a 2 um Nuclepore filter (=\nnanophytoplankton, 2-20 um). Two or three 1 liter bottles were filtered\nthrough a 20 um Nitex mesh then onto a GF/F filter (= 0.7-20 um).\\u00a0\nFilters were treated with 500 ul of 0.5 N HCl and left under a fumehood for 24\nhours, then combined with 10 ml scintillation cocktail.\\u00a0 Radioactivity\nwas determined in disintegrations per minute (DPM) by the shipboard liquid\nscintillation analyzer (Packard Tri-Carb 2000CA).\\u00a0\n \nRates of primary productivity (PP) were calculated in units of mg C m-3 d-1\nusing the methods of Barber et al. (1996) with the addition of dark bottles:\n \n\\u00a0\\u00a0\\u00a0 PP = (DPM24 \\u2013 DPM0 \\u2013 DPMd)/(1.05)(25200 mg C\nm-2)(DPMtot * time)-1\\u00a0\\u00a0\\u00a0 \\u00a0\\u00a0\\u00a0\n \nwhere DPM24 = activity on filter after 24 hour incubation; DPM0 = activity of\n(depth-specific) T0 particulate blank; DPMd = average of (depth-specific) dark\nbottles; DPMtot = total activity DPM of isotope added multiplied by volume of\nwater filtered (DPM ml-1); 1.05 = constant that accounts for preferential\nuptake of the lighter isotope 12C over 14C; 25,200 = concentration (in mg m-2)\nof inorganic carbon in seawater.\n \nThe rate of primary productivity for the picophytoplankton size class was\ndetermined by subtracting the nanophytoplankton productivity from the 0.7-20\num productivity. Primary productivity for the microphytoplankton size class\nwas determined by subtracting the 0.7-20 um productivity from the total\nprimary productivity, 0.7-200 um. Total and size-fractionated rates of primary\nproductivity were integrated to 100 meters using trapezoidal integration (mg C\nm-2 d-1).\n \nMicroscopy  \n Samples preserved in Lugol\\u2019s were settled overnight in a 100 ml\nsedimentation chamber and enumerated at 400x using a Nikon TS-100 Eclipse\ninverted microscope. A minimum of 400 cells per sample were counted to give a\nconfidence interval of \\u00b110 % (Guillard, 1973). Phytoplankton taxa were\nidentified to the lowest taxonomic level possible, that is, in most cases, to\ngenus.\n \nHPLC and ChemTax  \n Samples for HPLC analysis were lyophilized for 24 h at -50\\u00b0 C, placed\nin 90% acetone (0.45-0.55 ml), and extracted at -20\\u00b0 C for 24 h.\\u00a0\nFiltered extracts (350 \\u00b5l) were injected into a Shimadzu HPLC equipped\nwith a monomeric (Rainin Microsorb-MV, 0.46 x 10 cm, 3 \\u00b5m) and a\npolymeric (Vydac 201TP54, 0.46 x 25 cm, 5 um) reverse-phase C18 column in\nseries. A nonlinear binary gradient consisting of the solvents 80% methanol:\n20% 0.50 M ammonium acetate and 80% methanol: 20% acetone was used for pigment\nseparations (Pinckney et al. 1996). Absorption spectra and chromatograms (440\n\\u00b1 4 nm) were acquired using a Shimadzu SPD-M10av photodiode array\ndetector. Pigment peaks were identified by comparison of retention times and\nabsorption spectra with pure standards (DHI, Denmark). The synthetic\ncarotenoid \\u00df-apo-8'-carotenal (Sigma) was used as an internal standard.\nContributions of individual algal groups to total community composition and to\neach size class was determined by chemical taxonomy using the ChemTax matrix\n(Mackey et al., 1996).
attribute NC_GLOBAL awards_0_award_nid String 54642
attribute NC_GLOBAL awards_0_award_number String OCE-1030345
attribute NC_GLOBAL awards_0_data_url String http://www.nsf.gov/awardsearch/showAward.do?AwardNumber=1030345 (external link)
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 ChemTax-based Chl-a in Algal Classes \n  (Reported as ug/L of chlorohyll a in each class) \n Project: Trophic BATS \n PI: Tammi L. Richardson (U. of S. Carolina) \n Co-PIs: Rob Condon (DISL) & Susanna Neuer (Arizona State U.) \n Version: 17 June 2013 \n  \n Note: 'nd' = 'not determined'.
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/ (external link)
attribute NC_GLOBAL data_source String extract_data_as_tsv version 2.3  19 Dec 2019
attribute NC_GLOBAL date_created String 2013-03-11T16:00:14Z
attribute NC_GLOBAL date_modified String 2019-11-01T15:34:31Z
attribute NC_GLOBAL defaultDataQuery String &time<now
attribute NC_GLOBAL doi String 10.1575/1912/bco-dmo.3885.1
attribute NC_GLOBAL Easternmost_Easting double -63.4806
attribute NC_GLOBAL geospatial_lat_max double 33.5007
attribute NC_GLOBAL geospatial_lat_min double 29.5474
attribute NC_GLOBAL geospatial_lat_units String degrees_north
attribute NC_GLOBAL geospatial_lon_max double -63.4806
attribute NC_GLOBAL geospatial_lon_min double -65.7996
attribute NC_GLOBAL geospatial_lon_units String degrees_east
attribute NC_GLOBAL geospatial_vertical_max double 200.0
attribute NC_GLOBAL geospatial_vertical_min double 1.0
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/3885 (external link)
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 Samples were obtained using the 24 bottle Niskin rosette from 3-4 depths.
attribute NC_GLOBAL instruments_0_dataset_instrument_nid String 6102
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/ (external link)
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 SBE 9
attribute NC_GLOBAL instruments_1_dataset_instrument_description String CTD casts were perfomed using a Sea-Bird Electronics SBE-09 plus (24 bottle Niskin rosette).
attribute NC_GLOBAL instruments_1_dataset_instrument_nid String 6101
attribute NC_GLOBAL instruments_1_description String The Sea-Bird SBE 9 is a type of CTD instrument package.  The SBE 9 is the Underwater Unit and is most often combined with the SBE 11 Deck Unit (for real-time readout using conductive wire) when deployed from a research vessel. The combination of the SBE 9 and SBE 11 is called a SBE 911.  The SBE 9 uses Sea-Bird's standard modular temperature and conductivity sensors (SBE 3 and SBE 4). The SBE 9 CTD can be configured with auxiliary sensors to measure other parameters including dissolved oxygen, pH, turbidity, fluorometer, altimeter, etc.). Note that in most cases, it is more accurate to specify SBE 911 than SBE 9 since it is likely a SBE 11 deck unit was used.  more information from Sea-Bird Electronics
attribute NC_GLOBAL instruments_1_instrument_external_identifier String https://vocab.nerc.ac.uk/collection/L05/current/130/ (external link)
attribute NC_GLOBAL instruments_1_instrument_name String CTD Sea-Bird 9
attribute NC_GLOBAL instruments_1_instrument_nid String 488
attribute NC_GLOBAL instruments_1_supplied_name String CTD Sea-Bird 9
attribute NC_GLOBAL instruments_2_acronym String HPLC
attribute NC_GLOBAL instruments_2_dataset_instrument_description String HPLC analysis was performed using a Shimadzu HPLC equipped with a  monomeric (Rainin Microsorb-MV, 0.46 x 10 cm, 3 µm) and a polymeric  (Vydac 201TP54, 0.46 x 25 cm, 5 um) reverse-phase C18 column in series.  Absorption spectra and chromatograms (440 ± 4 nm) were acquired using a  Shimadzu SPD-M10av photodiode array detector.
attribute NC_GLOBAL instruments_2_dataset_instrument_nid String 6103
attribute NC_GLOBAL instruments_2_description String A High-performance liquid chromatograph (HPLC) is a type of liquid chromatography used to separate compounds that are dissolved in solution. HPLC instruments consist of a reservoir of the mobile phase, a pump, an injector, a separation column, and a detector. Compounds are separated by high pressure pumping of the sample mixture onto a column packed with microspheres coated with the stationary phase. The different components in the mixture pass through the column at different rates due to differences in their partitioning behavior between the mobile liquid phase and the stationary phase.
attribute NC_GLOBAL instruments_2_instrument_external_identifier String https://vocab.nerc.ac.uk/collection/L05/current/LAB11/ (external link)
attribute NC_GLOBAL instruments_2_instrument_name String High Performance Liquid Chromatograph
attribute NC_GLOBAL instruments_2_instrument_nid String 506
attribute NC_GLOBAL instruments_2_supplied_name String High Performance Liquid Chromatograph
attribute NC_GLOBAL instruments_3_acronym String Inverted Microscope
attribute NC_GLOBAL instruments_3_dataset_instrument_description String Samples preserved in Lugol’s were settled overnight in a 100 ml  sedimentation chamber and enumerated at 400x using a Nikon TS-100  Eclipse inverted microscope
attribute NC_GLOBAL instruments_3_dataset_instrument_nid String 6222
attribute NC_GLOBAL instruments_3_description String An inverted microscope is a microscope with its light source and condenser on the top, above the stage pointing down, while the objectives and turret are below the stage pointing up. It was invented in 1850 by J. Lawrence Smith, a faculty member of Tulane University (then named the Medical College of Louisiana).\n\nInverted microscopes are useful for observing living cells or organisms at the bottom of a large container (e.g. a tissue culture flask) under more natural conditions than on a glass slide, as is the case with a conventional microscope. Inverted microscopes are also used in micromanipulation applications where space above the specimen is required for manipulator mechanisms and the microtools they hold, and in metallurgical applications where polished samples can be placed on top of the stage and viewed from underneath using reflecting objectives.\n\nThe stage on an inverted microscope is usually fixed, and focus is adjusted by moving the objective lens along a vertical axis to bring it closer to or further from the specimen. The focus mechanism typically has a dual concentric knob for coarse and fine adjustment. Depending on the size of the microscope, four to six objective lenses of different magnifications may be fitted to a rotating turret known as a nosepiece. These microscopes may also be fitted with accessories for fitting still and video cameras, fluorescence illumination, confocal scanning and many other applications.
attribute NC_GLOBAL instruments_3_instrument_external_identifier String https://vocab.nerc.ac.uk/collection/L05/current/LAB05/ (external link)
attribute NC_GLOBAL instruments_3_instrument_name String Inverted Microscope
attribute NC_GLOBAL instruments_3_instrument_nid String 675
attribute NC_GLOBAL instruments_3_supplied_name String Inverted Microscope
attribute NC_GLOBAL keywords String bco, bco-dmo, biological, cast, chemical, cruise, cruise_id, cryptophytes, cyanobacteria, data, dataset, date, date_gmt, depth, diatoms, dinoflagellates, dmo, erddap, fraction, haptophytes, iso, latitude, longitude, management, oceanography, office, pelagophytes, prasinophytes, preliminary, sample, size, size_fraction, time, time_gmt
attribute NC_GLOBAL license String https://www.bco-dmo.org/dataset/3885/license (external link)
attribute NC_GLOBAL metadata_source String https://www.bco-dmo.org/api/dataset/3885 (external link)
attribute NC_GLOBAL Northernmost_Northing double 33.5007
attribute NC_GLOBAL param_mapping String {'3885': {'lat': 'master - latitude', 'depth': 'flag - depth', 'lon': 'master - longitude', 'ISO_DateTime_UTC': 'master - time'}}
attribute NC_GLOBAL parameter_source String https://www.bco-dmo.org/mapserver/dataset/3885/parameters (external link)
attribute NC_GLOBAL people_0_affiliation String University of South Carolina
attribute NC_GLOBAL people_0_person_name String Tammi Richardson
attribute NC_GLOBAL people_0_person_nid String 50838
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 Dauphin Island Sea Lab
attribute NC_GLOBAL people_1_affiliation_acronym String DISL
attribute NC_GLOBAL people_1_person_name String Robert Condon
attribute NC_GLOBAL people_1_person_nid String 51335
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 Arizona State University
attribute NC_GLOBAL people_2_affiliation_acronym String ASU
attribute NC_GLOBAL people_2_person_name String Susanne Neuer
attribute NC_GLOBAL people_2_person_nid String 51336
attribute NC_GLOBAL people_2_role String Co-Principal Investigator
attribute NC_GLOBAL people_2_role_type String originator
attribute NC_GLOBAL people_3_affiliation String Woods Hole Oceanographic Institution
attribute NC_GLOBAL people_3_affiliation_acronym String WHOI BCO-DMO
attribute NC_GLOBAL people_3_person_name String Shannon Rauch
attribute NC_GLOBAL people_3_person_nid String 51498
attribute NC_GLOBAL people_3_role String BCO-DMO Data Manager
attribute NC_GLOBAL people_3_role_type String related
attribute NC_GLOBAL project String Trophic BATS
attribute NC_GLOBAL projects_0_acronym String Trophic BATS
attribute NC_GLOBAL projects_0_description String Fluxes of particulate carbon from the surface ocean are greatly influenced by the size, taxonomic composition and trophic interactions of the resident planktonic community. Large and/or heavily-ballasted phytoplankton such as diatoms and coccolithophores are key contributors to carbon export due to their high sinking rates and direct routes of export through large zooplankton. The potential contributions of small, unballasted phytoplankton, through aggregation and/or trophic re-packaging, have been recognized more recently. This recognition comes as direct observations in the field show unexpected trends. In the Sargasso Sea, for example, shallow carbon export has increased in the last decade but the corresponding shift in phytoplankton community composition during this time has not been towards larger cells like diatoms. Instead, the abundance of the picoplanktonic cyanobacterium, Synechococccus, has increased significantly. The trophic pathways that link the increased abundance of Synechococcus to carbon export have not been characterized. These observations helped to frame the overarching research question, \"How do plankton size, community composition and trophic interactions modify carbon export from the euphotic zone\". Since small phytoplankton are responsible for the majority of primary production in oligotrophic subtropical gyres, the trophic interactions that include them must be characterized in order to achieve a mechanistic understanding of the function of the biological pump in the oligotrophic regions of the ocean.\nThis requires a complete characterization of the major organisms and their rates of production and consumption. Accordingly, the research objectives are: 1) to characterize (qualitatively and quantitatively) trophic interactions between major plankton groups in the euphotic zone and rates of, and contributors to, carbon export and 2) to develop a constrained food web model, based on these data, that will allow us to better understand current and predict near-future patterns in export production in the Sargasso Sea.\nThe investigators will use a combination of field-based process studies and food web modeling to quantify rates of carbon exchange between key components of the ecosystem at the Bermuda Atlantic Time-series Study (BATS) site. Measurements will include a novel DNA-based approach to characterizing and quantifying planktonic contributors to carbon export. The well-documented seasonal variability at BATS and the occurrence of mesoscale eddies will be used as a natural laboratory in which to study ecosystems of different structure. This study is unique in that it aims to characterize multiple food web interactions and carbon export simultaneously and over similar time and space scales. A key strength of the proposed research is also the tight connection and feedback between the data collection and modeling components.\nCharacterizing the complex interactions between the biological community and export production is critical for predicting changes in phytoplankton species dominance, trophic relationships and export production that might occur under scenarios of climate-related changes in ocean circulation and mixing. The results from this research may also contribute to understanding of the biological mechanisms that drive current regional to basin scale variability in carbon export in oligotrophic gyres.
attribute NC_GLOBAL projects_0_end_date String 2014-09
attribute NC_GLOBAL projects_0_geolocation String Sargasso Sea, BATS site
attribute NC_GLOBAL projects_0_name String Plankton Community Composition and Trophic Interactions as Modifiers of Carbon Export in the Sargasso Sea
attribute NC_GLOBAL projects_0_project_nid String 2150
attribute NC_GLOBAL projects_0_start_date String 2010-10
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 29.5474
attribute NC_GLOBAL standard_name_vocabulary String CF Standard Name Table v55
attribute NC_GLOBAL summary String ChemTax based chl-a of algal groups are reported from four cruises in the Sargasso Sea during 2011 and 2012.
attribute NC_GLOBAL time_coverage_end String 2012-07-30T10:35:00Z
attribute NC_GLOBAL time_coverage_start String 2011-02-24T15:10:00Z
attribute NC_GLOBAL title String ChemTax based chl-a of algal groups from R/V Atlantic Explorer cruises AE1102, AE1118, AE1206, AE1219 in the Sargasso Sea, Bermuda Atlantic Time-Series Station (BATS) from 2011-2012 (Trophic BATS project)
attribute NC_GLOBAL version String 1
attribute NC_GLOBAL Westernmost_Easting double -65.7996
attribute NC_GLOBAL xml_source String osprey2erddap.update_xml() v1.3
variable cruise_id String
attribute cruise_id bcodmo_name String cruise_id
attribute cruise_id description String Official cruise identifier e.g. AE1102 = R/V Atlantic  Explorer cruise number 1102.
attribute cruise_id long_name String Cruise Id
attribute cruise_id units String dimensionless
variable date_gmt String
attribute date_gmt bcodmo_name String date_gmt
attribute date_gmt description String Date of sample collection (GMT) in mmddYYYY format.
attribute date_gmt long_name String Date Gmt
attribute date_gmt units String unitless
variable cast byte
attribute cast _FillValue byte 127
attribute cast actual_range byte 1, 39
attribute cast bcodmo_name String cast
attribute cast description String CTD cast number.
attribute cast long_name String Cast
attribute cast units String dimensionless
variable time_gmt String
attribute time_gmt bcodmo_name String time_gmt
attribute time_gmt description String Time of sample collection (GMT); 24-hour clock.
attribute time_gmt long_name String Time Gmt
attribute time_gmt units String HHMM
variable latitude double
attribute latitude _CoordinateAxisType String Lat
attribute latitude _FillValue double NaN
attribute latitude actual_range double 29.5474, 33.5007
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. Positive values = North.
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/ (external link)
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 -65.7996, -63.4806
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. Positive values = East.
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/ (external link)
attribute longitude standard_name String longitude
attribute longitude units String degrees_east
variable time double
attribute time _CoordinateAxisType String Time
attribute time actual_range double 1.2985602E9, 1.3436445E9
attribute time axis String T
attribute time bcodmo_name String ISO_DateTime_UTC
attribute time description String Date/Time (UTC) formatted to ISO 8601 standard in YYYY-mm-ddTHH:MM:SS.ssZ format. T indicates start of time string; Z indicates UTC.
attribute time ioos_category String Time
attribute time long_name String ISO Date Time UTC
attribute time nerc_identifier String https://vocab.nerc.ac.uk/collection/P01/current/DTUT8601/ (external link)
attribute time source_name String ISO_DateTime_UTC
attribute time standard_name String time
attribute time time_origin String 01-JAN-1970 00:00:00
attribute time time_precision String 1970-01-01T00:00:00Z
attribute time units String seconds since 1970-01-01T00:00:00Z
variable depth double
attribute depth _CoordinateAxisType String Height
attribute depth _CoordinateZisPositive String down
attribute depth _FillValue double NaN
attribute depth actual_range double 1.0, 200.0
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 Sample depth.
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/ (external link)
attribute depth positive String down
attribute depth standard_name String depth
attribute depth units String m
variable sample String
attribute sample bcodmo_name String sample
attribute sample description String Sample identification number.
attribute sample long_name String Sample
attribute sample nerc_identifier String https://vocab.nerc.ac.uk/collection/P02/current/ACYC/ (external link)
attribute sample units String dimensionless
variable size_fraction String
attribute size_fraction bcodmo_name String unknown
attribute size_fraction description String Size fraction; whole = whole water (not pre-screened).
attribute size_fraction long_name String Size Fraction
attribute size_fraction units String micrometers
variable cyanobacteria float
attribute cyanobacteria _FillValue float NaN
attribute cyanobacteria actual_range float 0.0, 6.547
attribute cyanobacteria bcodmo_name String chlorophyll a
attribute cyanobacteria description String Contribution by cyanobacteria to total community composition measured in ug/L of Chlorophyll-a.
attribute cyanobacteria long_name String Cyanobacteria
attribute cyanobacteria nerc_identifier String https://vocab.nerc.ac.uk/collection/P01/current/CPHLHPP1/ (external link)
attribute cyanobacteria units String micrograms of Chl-a per liter
variable prasinophytes float
attribute prasinophytes _FillValue float NaN
attribute prasinophytes actual_range float 0.0, 2.612
attribute prasinophytes bcodmo_name String chlorophyll a
attribute prasinophytes description String Contribution by prasinophytes to total community composition measured in ug/L of Chlorophyll-a.
attribute prasinophytes long_name String Prasinophytes
attribute prasinophytes nerc_identifier String https://vocab.nerc.ac.uk/collection/P01/current/CPHLHPP1/ (external link)
attribute prasinophytes units String micrograms of Chl-a per liter
variable cryptophytes float
attribute cryptophytes _FillValue float NaN
attribute cryptophytes actual_range float 0.0, 0.111
attribute cryptophytes bcodmo_name String chlorophyll a
attribute cryptophytes description String Contribution by cryptophytes to total community composition measured in ug/L of Chlorophyll-a.
attribute cryptophytes long_name String Cryptophytes
attribute cryptophytes nerc_identifier String https://vocab.nerc.ac.uk/collection/P01/current/CPHLHPP1/ (external link)
attribute cryptophytes units String micrograms of Chl-a per liter
variable diatoms float
attribute diatoms _FillValue float NaN
attribute diatoms actual_range float 0.0, 0.073
attribute diatoms bcodmo_name String chlorophyll a
attribute diatoms description String Contribution by diatoms to total community composition measured in ug/L of Chlorophyll-a.
attribute diatoms long_name String Diatoms
attribute diatoms nerc_identifier String https://vocab.nerc.ac.uk/collection/P01/current/CPHLHPP1/ (external link)
attribute diatoms units String micrograms of Chl-a per liter
variable pelagophytes float
attribute pelagophytes _FillValue float NaN
attribute pelagophytes actual_range float 0.0, 0.407
attribute pelagophytes bcodmo_name String chlorophyll a
attribute pelagophytes description String Contribution by pelagophytes to total community composition measured in ug/L of Chlorophyll-a.
attribute pelagophytes long_name String Pelagophytes
attribute pelagophytes nerc_identifier String https://vocab.nerc.ac.uk/collection/P01/current/CPHLHPP1/ (external link)
attribute pelagophytes units String micrograms of Chl-a per liter
variable haptophytes float
attribute haptophytes _FillValue float NaN
attribute haptophytes actual_range float 0.0, 2.844
attribute haptophytes bcodmo_name String chlorophyll a
attribute haptophytes description String Contribution by haptophytes to total community composition measured in ug/L of Chlorophyll-a.
attribute haptophytes long_name String Haptophytes
attribute haptophytes nerc_identifier String https://vocab.nerc.ac.uk/collection/P01/current/CPHLHPP1/ (external link)
attribute haptophytes units String micrograms of Chl-a per liter
variable dinoflagellates float
attribute dinoflagellates _FillValue float NaN
attribute dinoflagellates actual_range float 0.0, 0.432
attribute dinoflagellates bcodmo_name String chlorophyll a
attribute dinoflagellates colorBarMaximum double 150.0
attribute dinoflagellates colorBarMinimum double 0.0
attribute dinoflagellates description String Contribution by dinoflagellates to total community composition measured in ug/L of Chlorophyll-a.
attribute dinoflagellates long_name String Dinoflagellates
attribute dinoflagellates nerc_identifier String https://vocab.nerc.ac.uk/collection/P01/current/CPHLHPP1/ (external link)
attribute dinoflagellates units String micrograms of Chl-a per liter

 
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