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282 results for “sanctuary”

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dryad36/100

Data from: Survivorship and growth in staghorn coral (Acropora cervicornis) outplanting projects in the Florida Keys National Marine Sanctuary

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publicApr 2020View details →
dryad36/100

Feeding observations on the Grizzled Giant Squirrel at Chinnar Wildlife Sanctuary, Southern Western Ghats, India

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publicDec 2023View details →
dryad36/100

Data from: Observational approaches to chimpanzee behavior in an African sanctuary: implications for research, welfare, and capacity-building

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publicJul 2023View details →
dryad36/100

Data from: Fish chorusing patterns in California (USA) National Marine Sanctuaries

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publicJul 2025View details →
dryad36/100

Data from: First dispersal records of the endangered Banteng (Bos javanicus) in Thung Yai Naresuan West Wildlife Sanctuary, Thailand

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publicJun 2024View details →
dryad36/100

Constructing visualization tools and training resources to assess climate impacts on the channel islands national marine sanctuary NetCDF files

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publicJun 2024View details →
dryad36/100

Mallard response to experimental human disturbance on sanctuary areas is mediated by hunting

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publicDec 2024View details →
zenodo32/100

Ginnaurgarh गिन्नोर्गढ़ (सिहोर जिला Madhya Pradesh). Śaiva sanctuary below fort, images.

<p>Ginnaurgarh गिन्नोर्गढ़ (सिहोर जिला Madhya Pradesh). Śaiva sanctuary below fort, detail of rock-cut images.</p>

opencc-by-4.0Feb 2020View details →
dryad32/100

Data from: Urban forest fragments as unexpected sanctuaries for the rare endemic ghost butterfly from the Atlantic forest.

Anthropogenic land expansion, particularly urbanization, is pervasive, dramatically modifies the environment and is a major threat to wildlife with its associated environmental stressors. Urban remnant vegetation can help mitigate these impacts and could be vital for species unable to survive in harsh urban environments. Although resembling non-urban habitats, urban vegetation remnants are subject to additional environmental stresses. Here we evaluate the occurrence and density of the endemic ghost butterfly (Morpho epistrophus nikolajewna), that was once common, in the highly fragmented Atlantic forest of NE Brazil. We tested whether this butterfly would be found at lower densities in urban forest fragments of contrasting sizes as opposed to rural ones, given the number of environmental stressors found in urban areas. We surveyed 14 forest fragments (range 2.8 to over 3000 ha) of semi-deciduous Atlantic forest in rural and urban locations using transect based distance sampling. The ghost butterflies showed strong seasonality; flying only from April to June. They were only identified in an urban fragment (515 ha), with an estimate of 720 individuals and a density 1.4 ind/ha. All forest fragments had experienced some level of logging in the past, which might have had an effect in the butterfly population. Nevertheless, rural forest fragments were subject to increased particulate matter concentrations, associated to biomass burning, that we suggest might have had a more influential role driving the collapse of rural populations. Our findings show the importance of urban forest remnants to sustain population of this endangered species.

opencc-zeroAug 2020View details →
dryad32/100

Data from: Group-level variation in co-feeding tolerance between two sanctuary-housed communities of chimpanzees (Pan troglodytes)

<p><span><span><span><span><span><span><span><span><span><span><span>Social tolerance in group-living animals can be viewed as a counterweight against competitive interests necessary to obtain coexistence equilibrium and maintain group cohesion. As such, it forms an interesting phenomenon to study at the group-level, but how can this be done most informatively? Here, we use three group-level co-feeding assays and social network analysis to study social tolerance in two groups of chimpanzees living under similar circumstances within a sanctuary to <i>i</i>) reassess whether social tolerance may be a group-specific parameter in chimpanzees and derive inferences about its long-term stability, and <i>ii</i>) compare the characteristics and resultant patterns between two established and one new assay. We show that the three assays expose the same (predicted) group-level differences in social tolerance as in the previous study eight years ago, thereby providing preliminary evidence for stability in group-specific levels of social tolerance in chimpanzees, despite changing group compositions. Furthermore, from an experimental point of view, we identify the new assay as more valid than the two established ones based on the consideration that resources may deplete at different rates across groups, which would consequently alter the need for tolerance differentially. We discuss implications for the study of social tolerance and highlight the importance of taking into account intraspecific variation in social animals.</span></span></span></span></span></span></span></span></span></span></span></p>

opencc-zeroDec 2020View details →
dryad32/100

Local-scale climatic refugia offer sanctuary for a habitat-forming species during a marine heatwave

<p><b>1. </b>Gradual climate change and discrete extreme climatic events have driven shifts in the structure of populations and the distribution of species in many marine ecosystems. The most profound impacts of recent warming trends have been generally observed at species' warm edges and on large conspicuous species. However, given that <span>different species and populations exhibit different responses to warming, and that responses are highly variable at regional scales, </span>there is a need <span>to broaden the evidence to include less conspicuous species and to focus on both local and regional scale processes.</span></p> <p><b>2. </b>We examined the population dynamics of canopy-forming seaweed populations situated at the core range of their distribution during a regional marine heatwave (MHW) event that occurred in the Mediterranean Sea in 2015, to determine between-site variability in relation to the intensity of the MHW. We combined field observations with a thermo-tolerance experiment to elucidate mechanisms underlying observed responses.</p> <p><b>3.</b> Despite our study populations are located in the species core range, the MHW was concomitant with a high mortality and structural shifts in only one of the two surveyed populations, most likely due to differences in habitat characteristics between sites (e.g. degree of shelter and seawater transfer). The experiment showed high mortalities at temperatures of 28 ºC, having the most severe implications for early life stages and fertility, which is consistent with warming being the cause of population changes in the field. Crucially, the regional-scale quantification of the MHW (as described by satellite-derived SSTs) did not capture local-scale variation in MHW conditions at the study sites, which likely explained variation in population-level responses to warming.</p> <p><b>4. </b><i>Synthesis.</i> Enclosed and semi-enclosed seas, such as the Mediterranean Sea, often highly impacted by human perturbations, are also global hotspots for ocean warming and are highly susceptible to future MHWs. Our findings highlight that local-scale variability in the magnitude of extreme climatic events can lead to local extinctions of already fragmented populations of habitat-forming seaweeds, even towards the species' core range. However, our results highlight the potential for local-scale climatic refugia, which could be identified and managed to safeguard the persistence of canopy-forming seaweeds.</p>

opencc-zeroJan 2021View details →
dryad32/100

Data from: Assessment of mesophotic coral ecosystem connectivity for proposed expansion of a marine sanctuary in the northwest Gulf of Mexico: population genetics

While there are several areas containing shallow coral habitats in the Gulf of Mexico (GOM), the availability of suitable reef habitat at mesophotic depths (~30–150 m) along the continental shelf margin suggests the potential for ecologically connected coral populations across hundreds of kilometers in the northwest (NW) GOM. The NW GOM includes a relatively high proportion of mesophotic habitats, including salt diapirs in Flower Garden Banks National Marine Sanctuary (FGBNMS), Bright Bank, and McGrail Bank, the latter two being Habitat Areas of Particular Concern (HAPCs). In response to a proposed expansion plan for the sanctuary boundaries to include additional mesophotic banks in the NW GOM, we investigated the genetic connectivity of the depth-generalist coral Montastraea cavernosa, a ubiquitous member of scleractinian communities throughout the Tropical Western Atlantic. Montastraea cavernosa populations in the NW GOM demonstrated strong connectivity with relatively high levels of gene flow and no significant genetic differentiation occurring over banks up to 120 km apart. Historical migration models based on genetic data predicted panmixia of M. cavernosa across the NW GOM. The comparisons between genetic and biophysical models (see Garavelli et al., 2018; associate manuscript) highlight not only the importance of incorporating multiple assessments of connectivity into management schemes, but also the potentially stochastic nature of oceanographic patterns in the NW GOM and their effect on migration estimates among coral habitats. These trends indicate that M. cavernosa populations have remained well-connected in the NW GOM and that coral populations on each bank have likely been receiving larval recruitment through time. Thus, M. cavernosa populations should be managed as a combined unit within the NW GOM, which supports the proposal to expand the NMS boundaries to include mesophotic habitats beyond West and East FGB.

opencc-zeroDec 2017View details →
zenodo32/100

FIGURE 2. a in A new species of Gegeneophis Peters (Amphibia: Gymnophiona: Caeciliidae) from the surroundings of Mookambika Wildlife Sanctuary, Karnataka, India

FIGURE 2. a. Dorsolateral view of the head, b. Ventral view of the head, c. Ventral view of the body terminus (photographs of the holotype of Gegeneophis madhavai in life).

opennotspecifiedDec 2004View details →
zenodo32/100

FIGURE 15 in Two new species of Lankascincus (Squamata: Scincidae) from Sripada Sanctuary (Peak Wilderness), in Sri Lanka

FIGURE 15. The results of Principle Component Analysis, showing first and second axes. LD—L. deignani, LM—L. munindradasai, LS—L. sripadensis, and LT—L. taprobanensis.

opennotspecifiedDec 2007View details →
zenodo32/100

FIGURE 14 in Two new species of Lankascincus (Squamata: Scincidae) from Sripada Sanctuary (Peak Wilderness), in Sri Lanka

FIGURE 14. Lankascinicus deignani Taylor (1950) paratype female 58 mm SVL FMNH131358 at Field Museum Natural History, USA. (photographed by Dr. Alan Resetar)

opennotspecifiedDec 2007View details →
zenodo32/100

FIGURE 9 in Two new species of Lankascincus (Squamata: Scincidae) from Sripada Sanctuary (Peak Wilderness), in Sri Lanka

FIGURE 9. The scale pattern of head of holotype male NMSL20070501, 58.27 mm SVL, A. the lateral view and B. the dorsal view.

opennotspecifiedDec 2007View details →
zenodo32/100

FIGURE 6 in Two new species of Lankascincus (Squamata: Scincidae) from Sripada Sanctuary (Peak Wilderness), in Sri Lanka

FIGURE 6. The ventral view of head of holotype male Lankascinicus munindradasai NMSL20072101, 40.16 mm SVL

opennotspecifiedDec 2007View details →
zenodo32/100

FIGURE 3 in Two new species of Lankascincus (Squamata: Scincidae) from Sripada Sanctuary (Peak Wilderness), in Sri Lanka

FIGURE 3. The scale pattern of head of holotype male Lankascinicus munindradasai NMSL20072101, 40.16 mm SVL, A. the lateral view and B. the dorsal view.

opennotspecifiedDec 2007View details →
zenodo32/100

FIGURE 5 in Two new species of Lankascincus (Squamata: Scincidae) from Sripada Sanctuary (Peak Wilderness), in Sri Lanka

FIGURE 5. The lateral view of head of holotype male Lankascinicus munindradasai NMSL20072101, 40.16 mm SVL

opennotspecifiedDec 2007View details →
zenodo32/100

FIGURE 4 in Two new species of Lankascincus (Squamata: Scincidae) from Sripada Sanctuary (Peak Wilderness), in Sri Lanka

FIGURE 4. The ventral view of palm and foot of holotype male Lankascinicus munindradasai NMSL20072101, 40.16 mm SVL

opennotspecifiedDec 2007View 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

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