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| griddap | Subset | tabledap | Make A Graph | wms | files | Title | Summary | FGDC | ISO 19115 | Info | Background Info | RSS | Institution | Dataset ID | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| https://pallter-data.marine.rutgers.edu/erddap/tabledap/IsotopicNicheWAPFoodWebComponents.subset | https://pallter-data.marine.rutgers.edu/erddap/tabledap/IsotopicNicheWAPFoodWebComponents | https://pallter-data.marine.rutgers.edu/erddap/tabledap/IsotopicNicheWAPFoodWebComponents.graph | https://pallter-data.marine.rutgers.edu/erddap/files/IsotopicNicheWAPFoodWebComponents/ | Isotopic signatures of penguin food-web components along the western Antarctic Peninsula, 2009-2011 | We evaluated regional variation in reproductive isotopic niche among breeding populations of Adélie (Pygoscelis adeliae), chinstrap (P. antarctica), and gentoo (P. papua) penguins west of the Antarctic Peninsula (AP) to test a hypothesis for sea ice-associated food-web correlates of breeding population change. We rely on signatures of naturally occurring carbon (13C/12C, δ13C) and nitrogen (15N/14N, δ15N) stable isotopes (SI) as integrated proxies of penguin trophic foraging and food-web structure. Each season, study nests, where pairs of adults were present, were individually marked and chosen before the onset of egg-laying, and consistently monitored. When study nests were found at the one-egg stage, both adults were captured to obtain blood samples used for molecular sexing and stable isotope analyses, and measurements of structural size and body mass. At the time of capture, each adult penguin was quickly blood sampled (~1 ml) from the brachial vein. After handling, individuals at study nests were further monitored to ensure the pair reached clutch completion, i.e., two eggs. At approximate an average nest age of five and 15 days, offspring from study nests were captured and quickly blood sampled (<= ~500 µl for day five chicks, and <= ~1 ml for day 15 chicks) from the tarsus vein using a sterile needle and heparinized capillary tubes for day five chicks, and a sterile 3 ml syringe and heparinized infusion needle for day 15 chicks, again to obtain blood tissue for SI analyses. Study nests were monitored for chick survival to 25 days. At five weeks into chick-rearing, older crèched chicks of all three species were captured and quickly blood sampled from study rookeries near Anvers Island. Handling of crèched chicks occurred over a one or two day period, which varied seasonally and by species depending on nest initiation dates. Adélie penguin chicks at Avian Island were sampled on the same day Anvers Island Adélie penguin chicks were sampled. Adélie penguin chicks at Charcot Island, sampled during one season only on 25 January 2010, were handled three days after Anvers Island and Avian Island Adélie penguin chicks were sampled that year, i.e., 22 January 2010. Blood samples from crèched chicks (~1 ml) were taken from the brachial vein using a sterile 3 ml syringe and heparinized infusion needle following sampling procedures used for adult penguins to obtain blood tissue for SI analyses. Stable isotope analyses were conducted at the Stable Isotope Facility at the University of California, Davis using an elemental analyzer interfaced with an isotope ratio mass spectrometer\n\ncdm_data_type = Other\nVARIABLES:\ntime (seconds since 1970-01-01T00:00:00Z)\n... (16 more variables)\n | https://pallter-data.marine.rutgers.edu/erddap/info/IsotopicNicheWAPFoodWebComponents/index.htmlTable | https://pal.lternet.edu/
| http://pallter-data.marine.rutgers.edu/erddap/rss/IsotopicNicheWAPFoodWebComponents.rss | https://pallter-data.marine.rutgers.edu/erddap/subscriptions/add.html?datasetID=IsotopicNicheWAPFoodWebComponents&showErrors=false&email= | National Science Foundation | IsotopicNicheWAPFoodWebComponents | ||||
| https://pallter-data.marine.rutgers.edu/erddap/tabledap/AdeliePenguinMicroSatellite.subset | https://pallter-data.marine.rutgers.edu/erddap/tabledap/AdeliePenguinMicroSatellite | https://pallter-data.marine.rutgers.edu/erddap/tabledap/AdeliePenguinMicroSatellite.graph | https://pallter-data.marine.rutgers.edu/erddap/files/AdeliePenguinMicroSatellite/ | Nuclear genetic markers used to infer population genetic structure among breeding Adelie penguins from four regional rookeries along the western Antarctic Peninsula, 2008-2011.\\n | We used nuclear and mitochondrial DNA (mtDNA, data archived in GenBank) markers to better understand historical population genetic structure and gene flow given relatively recent and ongoing reductions in sea ice habitats and changes in numbers of breeding adult Adelie penguins at regional rookeries along the western Antarctic Peninsula. Study nests near Anvers Island, where pairs of adults were present, were individually marked and chosen before the onset of egg-laying, and consistently monitored each season (2008-2009). When study nests were found at the one-egg stage, both adults were captured to obtain blood samples used for population genetic analyses. At the time of capture, each adult penguin was quickly blood sampled (~1 ml) from the brachial vein using a and non-heparinized, sterile 3 ml syringe infusion needle. After handling, individuals at study nests were further monitored to ensure the pair reached clutch completion, i.e., two eggs. Adélie penguin chicks at Avian Island were sampled over two years (2009-2010), Adelie chicks as Prospect Point were sampled during one year (2011), while chicks at Charcot Island were sampled during two seasons (2010-2011). Blood samples from crèched chicks (~1 ml) were taken from the brachial vein using a sterile 3 ml syringe and infusion needle following sampling procedures used for adult penguins. Genetic analyses were conducted at the wildlife genetics laboratory, Alaska Science Center - United States Geological Survey (USGS), under the supervision of geneticist Dr. S.L. Talbot.\\n\\nData presented here are raw data only and do not include any derived data products. For any meta-analyses with other microsatellite data, proper calibration across labs must be completed. Data were produced at the Alaska Science Center, USGS wildlife genetics laboratory under the supervision of Dr. Sandra Talbot (stalbot@usgs.gov). Questions regarding data or any laboratory cross-validation should be directed to Dr. Kristen Gorman (kgorman@sfu.ca).\n\ncdm_data_type = Other\nVARIABLES:\nstudy_name (Study)\nsample_number\nsample_number_region\nspecies\nregion\nreproductive_stage\nindividual_id\n... (21 more variables)\n | https://pallter-data.marine.rutgers.edu/erddap/info/AdeliePenguinMicroSatellite/index.htmlTable | https://pal.lternet.edu/
| http://pallter-data.marine.rutgers.edu/erddap/rss/AdeliePenguinMicroSatellite.rss | https://pallter-data.marine.rutgers.edu/erddap/subscriptions/add.html?datasetID=AdeliePenguinMicroSatellite&showErrors=false&email= | National Science Foundation | AdeliePenguinMicroSatellite | ||||
| https://pallter-data.marine.rutgers.edu/erddap/tabledap/StructuralSizeMeasurementsAndIsotopicSignaturesAdeliePenguins.subset | https://pallter-data.marine.rutgers.edu/erddap/tabledap/StructuralSizeMeasurementsAndIsotopicSignaturesAdeliePenguins | https://pallter-data.marine.rutgers.edu/erddap/tabledap/StructuralSizeMeasurementsAndIsotopicSignaturesAdeliePenguins.graph | https://pallter-data.marine.rutgers.edu/erddap/files/StructuralSizeMeasurementsAndIsotopicSignaturesAdeliePenguins/ | Structural size measurements and isotopic signatures of foraging among adult male and female Adélie penguins (Pygoscelis adeliae) nesting along the Palmer Archipelago near Palmer Station, 2007-2009 | Sexual segregation in vertebrate foraging niche is often associated with sexual size dimorphism (SSD), i.e., ecological sexual dimorphism. We examined ecological sexual dimorphism among sympatric nesting Pygoscelis penguins near Palmer Station, Antarctica, asking whether environmental variability in the form of winter sea ice is associated with differences in male and female pre-breeding foraging niche. Each season, study nests, where pairs of adults were present, were individually marked and chosen before the onset of egg-laying, and consistently monitored. When study nests were found at the one-egg stage, both adults were captured to obtain blood samples used for molecular sexing and stable isotope analyses, and measurements of structural size and body mass. At the time of capture, each adult penguin was quickly blood sampled (~1 ml) from the brachial vein. After handling, individuals at study nests were further monitored to ensure the pair reached clutch completion, i.e., two eggs. Molecular analyses were conducted at Simon Fraser University following standard PCR protocols, and stable isotope analyses were conducted at the Stable Isotope Facility at the University of California, Davis using an elemental analyzer interfaced with an isotope ratio mass spectrometer\n\ncdm_data_type = Other\nVARIABLES:\nstudy_name (Study)\nsample_number\nspecies\nregion\nisland_name\nreproductive_stage\nindividual_id\nfull_clutch\ntime (seconds since 1970-01-01T00:00:00Z)\nculmen_length (mm)\nculmen_depth (mm)\nflipper_length (mm)\nbody_mass (grams)\nsex\nratio_of_15n_to_14n (percent)\nratio_of_13c_to_12c (percent)\ncomments\n | https://pallter-data.marine.rutgers.edu/erddap/info/StructuralSizeMeasurementsAndIsotopicSignaturesAdeliePenguins/index.htmlTable | https://pal.lternet.edu/
| http://pallter-data.marine.rutgers.edu/erddap/rss/StructuralSizeMeasurementsAndIsotopicSignaturesAdeliePenguins.rss | https://pallter-data.marine.rutgers.edu/erddap/subscriptions/add.html?datasetID=StructuralSizeMeasurementsAndIsotopicSignaturesAdeliePenguins&showErrors=false&email= | National Science Foundation | StructuralSizeMeasurementsAndIsotopicSignaturesAdeliePenguins | ||||
| https://pallter-data.marine.rutgers.edu/erddap/tabledap/StructuralSizeMeasurementsAndIsotopicSignaturesChinstrapPenguins.subset | https://pallter-data.marine.rutgers.edu/erddap/tabledap/StructuralSizeMeasurementsAndIsotopicSignaturesChinstrapPenguins | https://pallter-data.marine.rutgers.edu/erddap/tabledap/StructuralSizeMeasurementsAndIsotopicSignaturesChinstrapPenguins.graph | https://pallter-data.marine.rutgers.edu/erddap/files/StructuralSizeMeasurementsAndIsotopicSignaturesChinstrapPenguins/ | Structural size measurements and isotopic signatures of foraging among adult male and female Chinstrap penguins (Pygoscelis antarcticus) nesting along the Palmer Archipelago near Palmer Station, 2007-2009 | Sexual segregation in vertebrate foraging niche is often associated with sexual size dimorphism (SSD), i.e., ecological sexual dimorphism. We examined ecological sexual dimorphism among sympatric nesting Pygoscelis penguins near Palmer Station, Antarctica, asking whether environmental variability in the form of winter sea ice is associated with differences in male and female pre-breeding foraging niche. Each season, study nests, where pairs of adults were present, were individually marked and chosen before the onset of egg-laying, and consistently monitored. When study nests were found at the one-egg stage, both adults were captured to obtain blood samples used for molecular sexing and stable isotope analyses, and measurements of structural size and body mass. At the time of capture, each adult penguin was quickly blood sampled (~1 ml) from the brachial vein. After handling, individuals at study nests were further monitored to ensure the pair reached clutch completion, i.e., two eggs. Molecular analyses were conducted at Simon Fraser University following standard PCR protocols, and stable isotope analyses were conducted at the Stable Isotope Facility at the University of California, Davis using an elemental analyzer interfaced with an isotope ratio mass spectrometer\n\ncdm_data_type = Other\nVARIABLES:\ntime (Date Egg, seconds since 1970-01-01T00:00:00Z)\nsample_number\nspecies\nregion\nisland_name (Island)\nreproductive_stage (Stage)\nindividual_id\nfull_clutch (Clutch Completion)\ndorsal_ridge_length (Culmen Length)\ndorsal_ridge_depth (Culmen Depth, mm)\nflipper_length\nbody_mass (grams)\nsex\nratio_15n_14n (Delta 15 N, 1)\nratio_13c_12c (Delta 13 C, 1)\nnotes (Comments)\n | https://pallter-data.marine.rutgers.edu/erddap/info/StructuralSizeMeasurementsAndIsotopicSignaturesChinstrapPenguins/index.htmlTable | https://pal.lternet.edu/
| http://pallter-data.marine.rutgers.edu/erddap/rss/StructuralSizeMeasurementsAndIsotopicSignaturesChinstrapPenguins.rss | https://pallter-data.marine.rutgers.edu/erddap/subscriptions/add.html?datasetID=StructuralSizeMeasurementsAndIsotopicSignaturesChinstrapPenguins&showErrors=false&email= | National Science Foundation | StructuralSizeMeasurementsAndIsotopicSignaturesChinstrapPenguins | ||||
| https://pallter-data.marine.rutgers.edu/erddap/tabledap/StructuralSizeMeasurementsAndIsotopicSignaturesGentooPenguins.subset | https://pallter-data.marine.rutgers.edu/erddap/tabledap/StructuralSizeMeasurementsAndIsotopicSignaturesGentooPenguins | https://pallter-data.marine.rutgers.edu/erddap/tabledap/StructuralSizeMeasurementsAndIsotopicSignaturesGentooPenguins.graph | https://pallter-data.marine.rutgers.edu/erddap/files/StructuralSizeMeasurementsAndIsotopicSignaturesGentooPenguins/ | Structural size measurements and isotopic signatures of foraging among adult male and female gentoo penguins (Pygoscelis papua) nesting along the Palmer Archipelago near Palmer Station, 2007-2009 | Sexual segregation in vertebrate foraging niche is often associated with sexual size dimorphism (SSD), i.e., ecological sexual dimorphism. We examined ecological sexual dimorphism among sympatric nesting Pygoscelis penguins near Palmer Station, Antarctica, asking whether environmental variability in the form of winter sea ice is associated with differences in male and female pre-breeding foraging niche. Each season, study nests, where pairs of adults were present, were individually marked and chosen before the onset of egg-laying, and consistently monitored. When study nests were found at the one-egg stage, both adults were captured to obtain blood samples used for molecular sexing and stable isotope analyses, and measurements of structural size and body mass. At the time of capture, each adult penguin was quickly blood sampled (~1 ml) from the brachial vein. After handling, individuals at study nests were further monitored to ensure the pair reached clutch completion, i.e., two eggs. Molecular analyses were conducted at Simon Fraser University following standard PCR protocols, and stable isotope analyses were conducted at the Stable Isotope Facility at the University of California, Davis using an elemental analyzer interfaced with an isotope ratio mass spectrometer\n\ncdm_data_type = Other\nVARIABLES:\nstudy_name (Study)\nsample_number\nspecies\nregion\nisland_name\nreproductive_stage\nindividual_id\nfull_clutch\ntime (seconds since 1970-01-01T00:00:00Z)\nculmen_length (mm)\nculmen_depth (mm)\nflipper_length (mm)\nbody_mass (grams)\nsex\nratio_of_15n_to_14n (percent)\nratio_of_13c_to_12c (percent)\ncomments\n | https://pallter-data.marine.rutgers.edu/erddap/info/StructuralSizeMeasurementsAndIsotopicSignaturesGentooPenguins/index.htmlTable | https://pal.lternet.edu/
| http://pallter-data.marine.rutgers.edu/erddap/rss/StructuralSizeMeasurementsAndIsotopicSignaturesGentooPenguins.rss | https://pallter-data.marine.rutgers.edu/erddap/subscriptions/add.html?datasetID=StructuralSizeMeasurementsAndIsotopicSignaturesGentooPenguins&showErrors=false&email= | National Science Foundation | StructuralSizeMeasurementsAndIsotopicSignaturesGentooPenguins |