These data were used for an analysis of Steller sea lion pup health and condition by Lander et al. (2013). Serum chemistry and hematological values were measured by analysis of blood samples taken from 1,231 Steller sea lion pups (<2 months old). Pups were captured by hand or with hoop nets at 37 rookeries across their Alaskan range during mid-June to early July. Blood samples were collected from the caudal gluteal vein into EDTA and serum separator tubes. For details on analytical methodology, see Lander et al. (2013).

The data consist of blood chemistry and hematology from sea otters captured at sites along the Aleutian archipelago, the Alaska Peninsula, the Gulf of Alaska, and Prince William sound between 2004 and 2012. The data include the blood chemistry and hematology findings as well as general capture location, if the sea otter population in that area is declining, capture date, age estimate, age class, sex, and a unique sea otter number connecting the sample to gene expression data.

The data consist of blood chemistry and hematology from sea otters captured at sites along the Aleutian archipelago, the Alaska Peninsula, the Gulf of Alaska, and Prince William sound between 2004 and 2012. The data include the blood chemistry and hematology findings as well as general capture location, if the sea otter population in that area is declining, capture date, age estimate, age class, sex, and a unique sea otter number connecting the sample to gene expression data.

This data set contains information on blood chemistry and hematological parameters of captive Pacific Common Eiders (Somateria mollissima v-nigrum) for reference periods and after satellite transmitter implantation. These data were collected for health assessments, to evaluate seasonal changes in regularly measured biomarkers, to assess the physiological responses to dive conditioning, and to measure responses to surgical implantation of a satellite transmitter.

Three data sets are included here to aid in assessment of the sea otter population collapse in southwest Alaska. One data set consists of results of sea otter surveys conducted between 1959 and 2015 at Bering Island, Russia and a selection of western Aleutian Islands in Alaska. Sea otter counts are reduced to a comparable value of otters per linear kilometer. Another data set consists per-capita and per kilometer recovery rates of stranded sea otter carcasses from locations ranging from Bering Island, Russia, several Aleutian Islands, sites along the Alaska Peninsula, and Prince William Sound, Alaska. These data are mainly from the period 1991-2009 and are from stable populations as well as those in decline or post decline. The third data set consists of blood chemistry and hematology of sea otters captured from along this same north Pacific region from 2004-2012. This data set can be used to help assess sea otter health in this region. Gene transcription data from some of the subject sea otters can be found at Bowen, L., Ballachey, B. E., Bodkin, J. L., Miles, A. K., Esler, D. and Kloecker, K. A., 2017, Sea Otter Gene Transcription Data from Kodiak, the Alaska Peninsula, and Prince William Sound, Alaska, 2005-2012: U.S. Geological Survey data release, https://doi.org/10.5066/F789141P. These data support the following publication: M. Tim Tinker, James L. Bodkin, Lizabeth Bowen, Brenda Ballachey, Gena Bentall, Alexander Burdin, Heather Coletti, George Esslinger, Brian B. Hatfield, Michael C. Kenner, Kimberly Kloecker, Brenda Konar, A. Keith Miles, Daniel H. Monson, Michael J. Murray, Ben Weitzman and James A. Estes, 2021, Sea otter population collapse in southwest Alaska: assessing ecological covariates, consequences, and causal factors: Ecological Monographs

This data set contains Steller sea lion diet data based on analysis of scats collected during summer (May-September) and winter (November-April) rookeries and haulouts in Alaska during 1990 to 2009. Prey items from 87 prey taxa were identified using hard parts including bones, otoliths, and cephalopod beaks. Frequency of occurrence was calculated for 375 site-year-season combinations, and used in the analysis published by Sinclair et al. (2013). This dataset includes the thirteen primary prey taxa (frequency of occurrence >= 5%) identified in the Sinclair et al. (2013) study.

This database contains counts of Steller sea lion pups on rookeries in Alaska made between 1961 and 2019. Pup counts are conducted in June-July. Pups are counted from the ground (by walking along the rookery), from cliff-side overlooks, and from aerial images (vertical orientation). Pup counts conducted in late June-mid July are considered to represent a complete census of pups produced at each site during the year.

These data are in four tables relating to complete blood count (CBC), biochemistry, blood gas analysis, corticosterone, serum protein electrophoresis, and sample attribute data of adult Pacific (Gavia pacifica) and Red-throated Loons (G. stellata) breeding in northern Alaska in 2023.

This dataset is one table with data collected and derived from polar bears sampled in Alaska's southern Beaufort Sea during 1983-2018. Collected data includes demographic and morphometric information. Derived data includes blood-based analyte values determined from whole blood and serum samples. Serum samples were analyzed on an Abaxis VS2 Biochemistry Analyzer and whole blood samples were analyzed on an Abaxis HM5 Diagnostic Analyzer. VS2 analysis quantified values of 13 biochemistry analytes for the period 1983-2016. Complete blood count (CBC) analyte values were quantified from the HM5 analysis for the period 2005-2018. These data were used to (i) generate reference ranges of serum biochemistry analyte values for healthy polar bears (Fry et al. 2019), and (ii) examine factors that may influence biochemistry and CBC analyte values over time (Fry et al. 2023).

This database contains counts of adult and juvenile (non-pup) Steller sea lions on rookeries and haulouts in Alaska made between 1904 and 2019. Non-pup counts have been conducted throughout the year. Breeding season (June-mid July) non-pup counts are used for population trend analysis, while counts at other times are used for analyses of distribution and for other purposes. Non-pups are counted from the ground (by walking along the rookery), from cliff-side overlooks, and from aerial imagery (oblique and vertical orientation). Non-pup counts represent only a fraction of the total number of animals that may use a site. Sea lions haul-out less frequently in winter than in summer; thus, winter counts represent a smaller fraction of the total population than summer counts.