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184 results for “Marine mammals”

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dryad32/100

Data from: Risk of extinction of a unique skate population due to predation by a recovering marine mammal

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publicJul 2020View details →
dryad32/100

Climate change impacts on seabirds and marine mammals: the importance of study duration, thermal tolerance and generation time

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publicNov 2021View details →
dryad32/100

Data from: The contrasting hidden consequences of parasitism: effects of a hematophagous nematode (Uncinaria sp.) in the development of a marine mammal swimming behavior.

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publicMar 2019View details →
dryad32/100

Data from: Accelerometers can measure total and activity-specific energy expenditure in free-ranging marine mammals only if linked to time-activity budgets

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publicAug 2017View details →
dryad32/100

Panmixia in a sea ice-associated marine mammal: evaluating genetic structure of the Pacific walrus (Odobenus rosmarus divergens) at multiple spatial scales

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publicFeb 2020View details →
dryad32/100

Raw data for predicting sample success for large-scale ancient DNA studies on marine mammals

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publicJan 2021View details →
dryad32/100

Data from: Acoustic risk balancing by marine mammals: anthropogenic noise can influence the foraging decisions by seals

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publicJun 2021View details →
dryad32/100

Data from: Marine strontium isotopes preserved in fossil shark teeth calibrate Neogene land mammal evolution

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publicJan 2025View details →
dryad32/100

Advances in thermal physiology of diving marine mammals: The dual role of peripheral perfusion

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publicOct 2021View details →
edi32/100

At-sea seabird censuses. Data on the species encountered (including marine mammals), their abundance, distribution and behavior. Data collected aboard cruises off the coast of the Western Antarctic Penninsula, 1993 - 2018.

The objectives of the LTER seabird component during the 92-93 season cruises were similar. These objectives included 1) determining the pelagic abundance and distribution of Adelie Penguins, 2) examining how the physical and biological characteristics of the marine environment influence these parameters and, 3) using these data to identify foraging areas that may be important to Adelie populations being studied as part of land-based work at Palmer Station. Secondary objectives included documenting the abundance and distribution of other seabirds and marine mammals within the LTER study area. The focus of the January cruise was the nearshore foraging habitat,which required sampling at smaller scales. All seabird censuses were thus conducted within approximately 100 kms of Palmer Station while traversing a sampling grid with stations at 10km intervals. The first two days (18-20 January) of this cruise were spent covering the selected grid as rapidly as possible resulting in 45 transects spaced at 45-60 minute intervals. There were no stops at the 10km stations during this Fast Grid phase. Upon completion of the Fast Grid, a force 12 gale suspended data collection for 24 hours. From January 22-25 the grid direction was reversed and the grid repeated. During this Slow Grid phase, 2-M net tows were done at 10km intervals and BOPS and 1-M and 2-M net tows every 20 km. All seabird censuses during the cruise were done using the procedures outlined in the previous paragraph.

openCustomFeb 2020View details →
edi32/100

At-sea seabird censuses. Data on the species encountered (including marine mammals), their abundance, distribution and behavior. Data collected aboard cruises off the coast of the Western Antarctic Penninsula, 1993, 1999 and 2001.

The objectives of the LTER seabird component during the 92-93 season cruises were similar. These objectives included 1) determining the pelagic abundance and distribution of Adelie Penguins, 2) examining how the physical and biological characteristics of the marine environment influence these parameters and, 3) using these data to identify foraging areas that may be important to Adelie populations being studied as part of land-based work at Palmer Station. Secondary objectives included documenting the abundance and distribution of other seabirds and marine mammals within the LTER study area. The focus of the January cruise was the nearshore foraging habitat,which required sampling at smaller scales. All seabird censuses were thus conducted within approximately 100 kms of Palmer Station while traversing a sampling grid with stations at 10km intervals. The first two days (18-20 January) of this cruise were spent covering the selected grid as rapidly as possible resulting in 45 transects spaced at 45-60 minute intervals. There were no stops at the 10km stations during this Fast Grid phase. Upon completion of the Fast Grid, a force 12 gale suspended data collection for 24 hours. From January 22-25 the grid direction was reversed and the grid repeated. During this Slow Grid phase, 2-M net tows were done at 10km intervals and BOPS and 1-M and 2-M net tows every 20 km. All seabird censusesduring the cruise were done using the procedures outlined in theprevious paragraph.

openCustomMar 2017View details →
edi32/100

At-sea seabird censuses. Data on the species encountered (including marine mammals), their abundance, distribution and behavior. Data collected aboard cruises off the coast of the Western Antarctic Penninsula, 1993 - 2018.

The objectives of the LTER seabird component during the 92-93 season cruises were similar. These objectives included 1) determining the pelagic abundance and distribution of Adelie Penguins, 2) examining how the physical and biological characteristics of the marine environment influence these parameters and, 3) using these data to identify foraging areas that may be important to Adelie populations being studied as part of land-based work at Palmer Station. Secondary objectives included documenting the abundance and distribution of other seabirds and marine mammals within the LTER study area. The focus of the January cruise was the nearshore foraging habitat, which required sampling at smaller scales. All seabird censuses were thus conducted within approximately 100 kms of Palmer Station while traversing a sampling grid with stations at 10km intervals. The first two days (18-20 January) of this cruise were spent covering the selected grid as rapidly as possible resulting in 45 transects spaced at 45-60 minute intervals. There were no stops at the 10km stations during this Fast Grid phase. Upon completion of the Fast Grid, a force 12 gale suspended data collection for 24 hours. From January 22-25 the grid direction was reversed and the grid repeated. During this Slow Grid phase, 2-M net tows were done at 10km intervals and BOPS and 1-M and 2-M net tows every 20 km. All seabird censuses during the cruise were done using the procedures outlined in the previous paragraph. Seventy-two 30-minute transects and 15 station censuses were completed during the January cruise. Athough seabirds were widely distributed throughout the study area, the highest densities and greatest biomass occurred consistently within 2-5 km of Anvers Island and several major island groups to the south and west near the Antarctic Peninsula. Adelie Penguins were the dominant component of this seabird assemblage in terms of both abundance and biomass. South Polar Skuas ranked second and Black-browed Al

openCustomFeb 2020View details →
edi32/100

At-sea seabird censuses. Data on the species encountered (including marine mammals), their abundance, distribution and behavior. Data collected aboard cruises off the coast of the Western Antarctic Penninsula, 1993, 1999 and 2001.

The objectives of the LTER seabird component during the 92-93 season cruises were similar. These objectives included 1) determining the pelagic abundance and distribution of Adelie Penguins, 2) examining how the physical and biological characteristics of the marine environment influence these parameters and, 3) using these data to identify foraging areas that may be important to Adelie populations being studied as part of land-based work at Palmer Station. Secondary objectives included documenting the abundance and distribution of other seabirds and marine mammals within the LTER study area. The focus of the January cruise was the nearshore foraging habitat,which required sampling at smaller scales. All seabird censuses were thus conducted within approximately 100 kms of Palmer Station while traversing a sampling grid with stations at 10km intervals. The first two days (18-20 January) of this cruise were spent covering the selected grid as rapidly as possible resulting in 45 transects spaced at 45-60 minute intervals. There were no stops at the 10km stations during this Fast Grid phase. Upon completion of the Fast Grid, a force 12 gale suspended data collection for 24 hours. From January 22-25 the grid direction was reversed and the grid repeated. During this Slow Grid phase, 2-M net tows were done at 10km intervals and BOPS and 1-M and 2-M net tows every 20 km. All seabird censusesduring the cruise were done using the procedures outlined in theprevious paragraph.

openCustomMar 2017View details →
dryad28/100

Data from: Movement and seasonal energetics mediate vulnerability to disturbance in marine mammal populations

<p>In marine environments noise from human activities is increasing dramatically, causing animals to alter their behavior and forage less efficiently. These alterations incur energetic costs that can result in reproductive failure, death, and may ultimately influence population viability; yet the link between population dynamics and individual energetics is poorly understood. We present an energy budget model for simulating effects of acoustic disturbance on populations. It accounts for environmental variability and individual state, while incorporating realistic animal movements. Using harbor porpoises (<i>Phocoena phocoena</i>) as a case study, we evaluated population consequences of disturbance from seismic surveys and investigated underlying drivers of vulnerability. The framework reproduced empirical estimates of population structure and seasonal variations in energetics. The largest effects predicted for seismic surveys were in late summer and fall, and were unrelated to local abundance, but instead to lactation costs, water temperature, and body fat. Our results demonstrate that consideration of temporal variation in individual energetics and their link to costs associated with disturbances is imperative when predicting disturbance impacts. These mechanisms are general to animal species, and the framework presented here can be used for gaining new insights into the spatiotemporal variability of animal movements and energetics that control population dynamics.</p>

opencc-zeroOct 2020View details →
dryad28/100

Data from: Foraging and fasting can influence contaminant concentrations in animals: an example with mercury contamination in a free-ranging marine mammal

Large fluctuations in animal body mass in relation to life-history events can influence contaminant concentrations and toxicological risk. We quantified mercury concentrations in adult northern elephant seals (Mirounga angustirostris) before and after lengthy at sea foraging trips (n = 89) or fasting periods on land (n = 27), and showed that mercury concentrations in blood and muscle changed in response to these events. The highest blood mercury concentrations were observed after the breeding fast, whereas the highest muscle mercury concentrations were observed when seals returned to land to moult. Mean female blood mercury concentrations decreased by 30% across each of the two annual foraging trips, demonstrating a foraging-associated dilution of mercury concentrations as seals gained mass. Blood mercury concentrations increased by 103% and 24% across the breeding and moulting fasts, respectively, demonstrating a fasting-associated concentration of mercury as seals lost mass. In contrast to blood, mercury concentrations in female's muscle increased by 19% during the post-breeding foraging trip and did not change during the post-moulting foraging trip. While fasting, female muscle mercury concentrations increased 26% during breeding, but decreased 14% during moulting. Consequently, regardless of exposure, an animal's contaminant concentration can be markedly influenced by their annual life-history events.

opencc-zeroDec 2017View details →
zenodo28/100

Figure 6 in Pliocene marine mammals from the Whalers Bluff Formation of Portland, Victoria, Australia

Figure 6. cf. Tursiops sp. (Pliocene Whalers Bluff Formation, Portland, Victoria, Australia), right periotic, NMV P218266 (AC). A, ventral view. B, cranial view. C, medial view. D, lateral view. Scale bar equals 10 mm.

opencc-by-4.0Dec 2005View details →
zenodo28/100

Figure 8 in Pliocene marine mammals from the Whalers Bluff Formation of Portland, Victoria, Australia

Figure 8. Delphinidae gen. et sp. undet. A (Pliocene Whalers Bluff Formation, Portland, Victoria, Australia), right periotic, NMV P218264 (AC). A, ventral view. B, cranial view. C, medial view. D, lateral view. Scale bar equals 10 mm.

opencc-by-4.0Dec 2005View details →
zenodo28/100

FIGURE 4 in Feeding in marine mammals: An integration of evolution and ecology through time

FIGURE 4. Anatomical features associated with filter feeding in crabeater seal (Lobodon carcinophaga skull, public domain image), and gray whale (Eschrichtius robustus skull, authors' work).

opencc-by-4.0Dec 2020View details →
zenodo28/100

FIGURE 10 in Feeding in marine mammals: An integration of evolution and ecology through time

FIGURE 10. Odontoceti stem and familial level diversity through time. The group "Delphinoidea" includes Delphinidae, Monodontidae, and Phocoenidae, as well as extinct members of this crown group of uncertain phylogenetic placement. The "river dolphins" closely related to these taxa (Inioidea and Lipotidae) are plotted separately to emphasize their diversity in the fossil record compared to the present. "Ziphioidea" includes Ziphiidae and closely related stem taxa as identified by Bianucci et al. (2016). Dashed vertical lines: black, epoch boundaries; gray, age boundaries.

opencc-by-4.0Dec 2020View details →
zenodo28/100

FIGURE 6 in Feeding in marine mammals: An integration of evolution and ecology through time

FIGURE 6. Generic level diversity of marine mammal groups through time. Dashed vertical lines: black, epoch boundaries; gray, age boundaries. All silhouettes used in Figures 6-20 are the authors' own work.

opencc-by-4.0Dec 2020View details →

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Allen Brain Atlas

Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.

allen-brain-atlas
neuroscienceopenDocumentation, web resources, and API references are available online.
Last verified 2026-04-30Open record

Annotated Behaviour and Observability Dataset (ABODe)

ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.

abode-home-cage
behavioral-neuroscienceopenThe DataShare record exposes download links for annotations, documentation, license text, and the zipped per-snippet data directory.
Last verified 2026-04-30Open record

DANDI Archive for NWB datasets

DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.

dandi-nwb
electrophysiologyopenPublished Dandiset metadata and archive endpoints are available through the production DANDI API.
Last verified 2026-04-30Open record

International Brain Laboratory public data

The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.

ibl
behavioral-neuroscienceopenPublic sessions can be searched and loaded from the IBL public data server through ONE.
Last verified 2026-04-29Open record

OpenNeuro

OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.

openneuro
neuroscienceopenPublished datasets are available on demand over the internet.
Last verified 2026-04-29Open record