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ERDDAP
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griddap | Subset | tabledap | Make A Graph | wms | files | Title | Summary | FGDC | ISO 19115 | Info | Background Info | RSS | Institution | Dataset ID | |
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https://pallter-data.marine.rutgers.edu/erddap/tabledap/CruiseChlorophyll.subset | https://pallter-data.marine.rutgers.edu/erddap/tabledap/CruiseChlorophyll | https://pallter-data.marine.rutgers.edu/erddap/tabledap/CruiseChlorophyll.graph | https://pallter-data.marine.rutgers.edu/erddap/files/CruiseChlorophyll/ | Chlorophyll and phaeopigments from water column samples, collected at selected depths aboard Palmer LTER annual cruises off the coast of the Western Antarctic Peninsula, 1991 - 2019. | Phytoplankton chlorophyll sampling was led by Smith from 1991-2002, and then by Vernet from 2003-2008. Schofield is the third, and current lead, beginning in 2009. Methods have been kept consistent as much as possible over the full time series and different Principal Investigators. Chlorophyll a (Chl a) is the principal photosynthetic pigment of phytoplankton, and is used as a proxy measurement for estimating phytoplankton biomass in water samples. Chl a concentrations reflect the distribution of active phytoplankton spatially and with depth in the water column and their changes over time. Phaeopigments are non-photosynthetic pigments that are degradation products of phytoplankton chlorophylls which form during and after phytoplankton blooms. Water samples are collected throughout the water column along the Western Antarctic Peninsula at regular LTER grid stations where Conductivity, Temperature, Depth (CTD) casts are preformed and in surface waters at underway stations, where CTD casts are not done, using the ship's flow-through seawater system. Water samples are filtered onto GF/F filters, and filters kept frozen at -80°C until analysis at Palmer Station following the completion of the cruise. Fluorometric chlorophyll and phaeopigment analysis is conducted at Palmer Station through acetone extraction of the GF/F filters and measurement of the extract on a Turner 10AU Fluorometer. The primary source of error for phaeopigment measurement is Chlorophyll b. If high amounts of Chlorophyll b are present in the sample, phaeopigments may be overestimated.\n\ncdm_data_type = Trajectory\nVARIABLES:\nstudy_name (Study)\nchlorophyll_a (mass_concentration_of_chlorophyll_a_in_sea_water, mg m-3)\nphaeopigment (mg m-3)\nevent\nbottle\ntime (seconds since 1970-01-01T00:00:00Z)\ngrid_line\ngrid_station\nlatitude (degrees_north)\nlongitude (degrees_east)\ndepth (m)\n... (7 more variables)\n | https://pallter-data.marine.rutgers.edu/erddap/metadata/fgdc/xml/CruiseChlorophyll_fgdc.xml | https://pallter-data.marine.rutgers.edu/erddap/metadata/iso19115/xml/CruiseChlorophyll_iso19115.xml | https://pallter-data.marine.rutgers.edu/erddap/info/CruiseChlorophyll/index.htmlTable | https://pal.lternet.edu/![]() | http://pallter-data.marine.rutgers.edu/erddap/rss/CruiseChlorophyll.rss | https://pallter-data.marine.rutgers.edu/erddap/subscriptions/add.html?datasetID=CruiseChlorophyll&showErrors=false&email= | National Science Foundation | CruiseChlorophyll | ||
https://pallter-data.marine.rutgers.edu/erddap/tabledap/CruiseDissolvedOxygen.subset | https://pallter-data.marine.rutgers.edu/erddap/tabledap/CruiseDissolvedOxygen | https://pallter-data.marine.rutgers.edu/erddap/tabledap/CruiseDissolvedOxygen.graph | https://pallter-data.marine.rutgers.edu/erddap/files/CruiseDissolvedOxygen/ | Dissolved oxygen of discrete water column samples at selected depths collected aboard Palmer LTER annual cruises off the coast of the Western Antarctic Peninsula, 1993, 2012. | Dissolved oxygen of discrete water column samples at selected depths collected aboard Palmer LTER annual cruises off the coast of the Western Antarctic Peninsula, 1993 - 2012. Oxygen is produced by phytoplankton photosynthesis and consumed by respiration of phytoplankton, zooplankton and bacteria. Oxygen also enters and exits the ocean via physical exchange with the atmosphere. Oxygen concentrations in the surface ocean may be supersaturated by photosynthesis and turbulence enhancing air-sea exchange via bubble injection; or undersaturated due to excess respiration. In cases where exchange with the atmosphere is limited, and/or respiration exceeds photosynthesis, oxygen concentration can be reduced to very low levels (hypoxia) or entirely depleted (anoxia). This is uncommon in cold Antarctic Seas where respiration is depressed and oxygen solubility is enhanced by low temperature. Different water masses have characteristic oxygen concentrations which serve as tracers for diagnosing physical mixing and advection. Dissolved oxygen was analyzed by Winkler Titration (see Methods) in Conductivity, Temperature, Depth (CTD)-Rosette bottle samples at all depths sampled until 2012. This measurement was discontinued in 2013. The CTD has duplicate oxygen electrodes that provide continuous vertical profiles of oxygen concentration at all depths on all casts. The vessel also has continuous underway, Optode determination of dissolved oxygen in the surface (ship's intake at 6 meters depth) on all cruises. Finally we now routinely measure net community production by Equilibrator Inlet Mass Spectroscopy (EIMS) on LTER cruises\n\ncdm_data_type = Trajectory\nVARIABLES:\nstudy_name (Study)\ntime (seconds since 1970-01-01T00:00:00Z)\nlatitude (degrees_north)\nlongitude (degrees_east)\ndepth (m)\nevent\ngrid_line\ngrid_station\nbottle\noxygen_concentration (mL L-1)\noxygen_concentration_moles (micromoles L-1)\ncomments\n | https://pallter-data.marine.rutgers.edu/erddap/metadata/fgdc/xml/CruiseDissolvedOxygen_fgdc.xml | https://pallter-data.marine.rutgers.edu/erddap/metadata/iso19115/xml/CruiseDissolvedOxygen_iso19115.xml | https://pallter-data.marine.rutgers.edu/erddap/info/CruiseDissolvedOxygen/index.htmlTable | https://pal.lternet.edu/![]() | http://pallter-data.marine.rutgers.edu/erddap/rss/CruiseDissolvedOxygen.rss | https://pallter-data.marine.rutgers.edu/erddap/subscriptions/add.html?datasetID=CruiseDissolvedOxygen&showErrors=false&email= | National Science Foundation | CruiseDissolvedOxygen | ||
https://pallter-data.marine.rutgers.edu/erddap/tabledap/CruiseHighPerformanceLiquidChromatographyPigments.subset | https://pallter-data.marine.rutgers.edu/erddap/tabledap/CruiseHighPerformanceLiquidChromatographyPigments | https://pallter-data.marine.rutgers.edu/erddap/tabledap/CruiseHighPerformanceLiquidChromatographyPigments.graph | https://pallter-data.marine.rutgers.edu/erddap/files/CruiseHighPerformanceLiquidChromatographyPigments/ | Photosynthetic pigments of water column samples and analyzed with High Performance Liquid Chromatography (HPLC), collected aboard Palmer LTER annual cruises off the coast of the Western Antarctica Peninsula, 1991, 2016. | Photosynthetic pigments of water column samples and analyzed with High Performance Liquid Chromatography (HPLC), collected aboard Palmer LTER annual cruises off the coast of the Western Antarctica Peninsula, 1991 - 2016. Phytoplankton pigment sampling was led by Prezelin from 1991-1994, and then by Vernet from 1995-2008. Schofield is the third, and current lead, beginning in 2009. Methods have been kept consistent as much as possible over the full time series and different Principal Investigators. Phytoplankton have a suite of accessory pigments in addition to Chlorophyll a, including other Chlorophyll's (e.g. Chlorophyll b), Xanthophylls, and Carotenes. These accessory pigments can be used as chemotaxonomic markers to assess the composition and distribution of the phytoplankton community. For example, Fucoxanthin is a marker pigment of Diatoms, whereas Alloxanthin is a marker pigment of Cryptophytes. Accessory pigments also assist in photoacclimation and photoprotective processes. Water samples are collected throughout the water column along the Western Antarctic Peninsula at regular LTER grid stations where Conductivity, Temperature, Depth (CTD) casts are preformed and in surface waters at underway stations, where CTD casts are not done, using the ship's flow-through seawater system. Water samples are filtered onto GF/F filters, and filters kept frozen at -80C until analysis. HPLC analysis is completed following Wright et al (1991). Following the guidelines set by NASA SeaHARRE, we use an internal standard and replicate injects on the HPLC to track recovery and replicability of the pigment extraction methods and the HPLC. Data is unavailable for the LMG10-01 cruise due to instrumentation problems and for the LMG12-01 cruise due to a freezer failure which resulted in the loss of samples.\n\ncdm_data_type = Trajectory\nVARIABLES:\nstudy_name (Study)\nevent\ncast_number\nbottle\ntime (seconds since 1970-01-01T00:00:00Z)\nlatitude (degrees_north)\nlongitude (degrees_east)\ndepth (m)\ngrid_line\n... (29 more variables)\n | https://pallter-data.marine.rutgers.edu/erddap/metadata/fgdc/xml/CruiseHighPerformanceLiquidChromatographyPigments_fgdc.xml | https://pallter-data.marine.rutgers.edu/erddap/metadata/iso19115/xml/CruiseHighPerformanceLiquidChromatographyPigments_iso19115.xml | https://pallter-data.marine.rutgers.edu/erddap/info/CruiseHighPerformanceLiquidChromatographyPigments/index.htmlTable | https://pal.lternet.edu/![]() | http://pallter-data.marine.rutgers.edu/erddap/rss/CruiseHighPerformanceLiquidChromatographyPigments.rss | https://pallter-data.marine.rutgers.edu/erddap/subscriptions/add.html?datasetID=CruiseHighPerformanceLiquidChromatographyPigments&showErrors=false&email= | National Science Foundation | CruiseHighPerformanceLiquidChromatographyPigments | ||
https://pallter-data.marine.rutgers.edu/erddap/tabledap/CruisePrimaryProduction.subset | https://pallter-data.marine.rutgers.edu/erddap/tabledap/CruisePrimaryProduction | https://pallter-data.marine.rutgers.edu/erddap/tabledap/CruisePrimaryProduction.graph | https://pallter-data.marine.rutgers.edu/erddap/files/CruisePrimaryProduction/ | Water column primary production from inorganic carbon uptake for 24h at simulated in situ (SIS) light levels in deck incubators, collected aboard Palmer LTER annual cruises off the coast of the Western Antarctic Peninsula, 1995 - 2019. | Primary Production experiments were led by Vernet from 1995-2008. Schofield is the current lead, beginning in 2009. Methods have been kept consistent as much as possible over the full time series and different Principal Investigators. Primary production is the uptake of inorganic carbon and assimilation of it into organic matter by phytoplankton. Primary production rates, expressed as mgC per m3 per day were measured by the uptake of radioactive (14C) sodium bicarbonate. Water samples are collected throughout the water column along the Western Antarctic Peninsula at regular LTER grid stations where Conductivity, Temperature, Depth (CTD) casts are performed. Water is put into borosilicate bottles, inoculated with 1 uCi of NaH14CO3 per bottle, and incubated in an outdoor deck incubator. The incubator is plumbed to the ship sea water system to maintain ambient seawater temperature and bottles are screened to in situ light levels. The uptake of 14C-bicarbonate by the phytoplankton was measured in a scintillation counter after a 24-hour incubation period..Primary Production experiments were led by Vernet from 1995-2008. Schofield is the current lead, beginning in 2009. Methods have been kept consistent as much as possible over the full time series and different Principal Investigators. Primary production is the uptake of inorganic carbon and assimilation of it into organic matter by phytoplankton. Primary production rates, expressed as mgC per m3 per day were measured by the uptake of radioactive (14C) sodium bicarbonate. Water samples are collected throughout the water column along the Western Antarctic Peninsula at regular LTER grid stations where CTD casts are performed. Water is put into borosilicate bottles, inoculated with 1 uCi of NaH14CO3 per bottle, and incubated in an outdoor deck incubator. The incubator is plumbed to the ship sea water system to maintain ambient seawater temperature and bottles are screened to in situ light levels. The uptake of 14C-bicarbonate by the phytoplankton was measured in a scintillation counter after a 24-hour incubation period.\n\ncdm_data_type = Trajectory\nVARIABLES:\nstudy_name (Study)\ntime (seconds since 1970-01-01T00:00:00Z)\nlatitude (degrees_north)\nlongitude (degrees_east)\ndepth (m)\nevent\n... (7 more variables)\n | https://pallter-data.marine.rutgers.edu/erddap/metadata/fgdc/xml/CruisePrimaryProduction_fgdc.xml | https://pallter-data.marine.rutgers.edu/erddap/metadata/iso19115/xml/CruisePrimaryProduction_iso19115.xml | https://pallter-data.marine.rutgers.edu/erddap/info/CruisePrimaryProduction/index.htmlTable | https://pal.lternet.edu/![]() | http://pallter-data.marine.rutgers.edu/erddap/rss/CruisePrimaryProduction.rss | https://pallter-data.marine.rutgers.edu/erddap/subscriptions/add.html?datasetID=CruisePrimaryProduction&showErrors=false&email= | National Science Foundation | CruisePrimaryProduction | ||
https://pallter-data.marine.rutgers.edu/erddap/tabledap/ZooplanktonDensityCurrent.subset | https://pallter-data.marine.rutgers.edu/erddap/tabledap/ZooplanktonDensityCurrent | https://pallter-data.marine.rutgers.edu/erddap/tabledap/ZooplanktonDensityCurrent.graph | https://pallter-data.marine.rutgers.edu/erddap/files/ZooplanktonDensityCurrent/ | Zooplankton collected with a 2-m, 700-um net towed from surface to 120 m, aboard Palmer Station Antarctica LTER annual cruises off the western antarctic peninsula, 2009, 2019. | Zooplankton collected with a 2-m, 700-um net towed from surface to 120 m, aboard Palmer Station Antarctica LTER annual cruises off the western antarctic peninsula, 2009 - 2019. Zooplankton are a morphologically and taxonomically diverse group of animals. Many zooplankton feed on phytoplankton and thus provide a link between primary producers and higher trophic levels. Zooplankton density and biovolume were determined at grid stations on the annual LTER cruises along the western Antarctic Peninsula (WAP). Typically, zooplankton were collected with a 2x2 meter, 700um mesh net fitted with a flow meter and towed obliquely to 120m. Zooplankton distributions vary spatially due to water column characteristics, which affect their predators' distributions. As climate change continues to affect the WAP, the relative abundance of the various zooplankton components can also be expected to change.\\n\\n\n\ncdm_data_type = Trajectory\nVARIABLES:\ntime (Start Time, seconds since 1970-01-01T00:00:00Z)\nend_time (seconds since 1970-01-01T00:00:00Z)\ndepth (m)\nlatitude (degrees_north)\nlongitude (degrees_east)\nlat_end (Latitude, degrees_north)\nlon_end (Longitude, degrees_east)\ncruise_name\nevent\ncruise_tow_number\ngrid_line\ngrid_station\ntow_duration\nheading (degrees)\nspeed_over_ground\nwind_speed_start (Wind Speed, m s-1)\nnet_id\ntow_type\n... (90 more variables)\n | https://pallter-data.marine.rutgers.edu/erddap/metadata/fgdc/xml/ZooplanktonDensityCurrent_fgdc.xml | https://pallter-data.marine.rutgers.edu/erddap/metadata/iso19115/xml/ZooplanktonDensityCurrent_iso19115.xml | https://pallter-data.marine.rutgers.edu/erddap/info/ZooplanktonDensityCurrent/index.htmlTable | https://pal.lternet.edu/![]() | http://pallter-data.marine.rutgers.edu/erddap/rss/ZooplanktonDensityCurrent.rss | https://pallter-data.marine.rutgers.edu/erddap/subscriptions/add.html?datasetID=ZooplanktonDensityCurrent&showErrors=false&email= | National Science Foundation | ZooplanktonDensityCurrent |