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263 results for “Uplands”

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zenodo32/100

FIG. 4 in Small scale habitat preferences of Myotis daubentonii, Pipistrellus pipistrellus, and potential aerial prey in an upland river valley

FIG. 4. Relationship between aerial insect number (pooled for altitude and all habitat types) with air temperature (r² = 0.092)

opennotspecifiedNov 2017View details →
zenodo32/100

F. 7 in Small scale habitat preferences of Myotis daubentonii, Pipistrellus pipistrellus, and potential aerial prey in an upland river valley

F. 7. Bat activity expressed as 0 ± SD bat passes hr-1 in relation to habitat type (water state) of both M. daubentonii and IG P. pipistrellus, pooled for all four altitudes

opennotspecifiedNov 2017View details →
zenodo32/100

FIG. 6 in Small scale habitat preferences of Myotis daubentonii, Pipistrellus pipistrellus, and potential aerial prey in an upland river valley

FIG. 6. Percentage of most prevalent aerial insects found during the 40 nights of sweep net sampling along river Wharfe. Samples been pooled for altitude and habitat type. Insect families represented by <0.1 % not shown

opennotspecifiedNov 2017View details →
zenodo32/100

FIG. 3 in Small scale habitat preferences of Myotis daubentonii, Pipistrellus pipistrellus, and potential aerial prey in an upland river valley

FIG. 3. Mean ± SD of number of aerial insects caught with sweep net above water surface (and over grass = control), pooled for all four altitudes (n = 40 nights)

opennotspecifiedNov 2017View details →
zenodo32/100

FIG. 5 in Small scale habitat preferences of Myotis daubentonii, Pipistrellus pipistrellus, and potential aerial prey in an upland river valley

FIG. 5. Relationship between numbers of aerial insects caught with a sweep net (pooled for all altitudes and habitat types) above the water surface with minimum wind speed

opennotspecifiedNov 2017View details →
zenodo32/100

FIG. 2 in Small scale habitat preferences of Myotis daubentonii, Pipistrellus pipistrellus, and potential aerial prey in an upland river valley

FIG. 2. Wind direction (degrees) expressed as windroses at for 10 nights from highest (a) to lowest (d) altitudes along river Wharfe

opennotspecifiedNov 2017View details →
zenodo32/100

Data of aquatic macro invertebrates and environmental conditions of upland lakes at Amazon

<p>Data of aquatic macro invertebrates and environmental conditions of upland lakes at Amazon</p>

opencc-by-4.0May 2023View details →
dryad32/100

Data from: Habitat usage of Daubenton's bat (Myotis daubentonii), common pipistrelle (Pipistrellus pipistrellus), and soprano pipistrelle (Pipistrellus pygmaeus) in a North Wales upland river catchment

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publicMay 2019View details →
dryad32/100

Topography and logging structure liana community assemblages in an upland evergreen forest, Ghana

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publicMay 2025View details →
dryad32/100

Data from: Sensory drive does not explain reproductive character displacement of male acoustic signals in the Upland Chorus Frog (Pseudacris feriarum)

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publicJan 2014View details →
dryad32/100

Livestock grazing impacts upon components of the breeding productivity of a common upland insectivorous passerine: results from a long-term experiment

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publicApr 2020View details →
dryad32/100

Data from: Rewilding in the English Uplands: policy and practice

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publicSep 2019View details →
dryad32/100

Evaluating the success of upland hay meadow restoration in the North Pennines, UK, using green hay transfer

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publicFeb 2022View details →
dryad32/100

Detecting the presence of nesting nightjar in upland clear-fell using drone-mounted thermal cameras

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publicFeb 2021View details →
dryad32/100

Data from: Prescribed burning impacts on ecosystem services in the British uplands: a methodological critique of the EMBER project

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publicAug 2019View details →
dryad32/100

Data from: Upland rush management advocated by agri-environment schemes increases predation of artificial wader nests

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publicFeb 2021View details →
edi32/100

Effects of Salicaceae species litter type and moisture at 10 paired wetland by upland plots:Specialization, maintenance of diversity and ecosystem consequences of growth defense trade-offs in a model system: the hyper-diverse willow communities of Cedar Creek

Cedar Creek includes a diversity of habitats, which support an astonishing number of species (15) from a single evolutionary lineage: the willow family (Salicaceae). The physiological tolerances and abiotic mechanisms that maintain natural diversity in this hyper-diverse system are beginning to be understood; the role of biotic interactions, however, remains a major gap in understanding. We hypothesize that insect herbivory plays a critical role in niche partitioning, providing an important explanation for high willow diversity. Using a replicated series of common gardens and insect herbivore manipulations in resource rich and resource poor habitats, we are testing for evolved trade-offs between defense investment and growth rate. We expect specialized plant syndromes to emerge along the continuum from ???herbivore escape??? via fast growth in high resource environments to ???anti-herbivore protection??? via heavy investment in defense in low resource environments. Evolved growth/defense strategies that promote diversity are also likely to have ecosystem consequences due to foliar chemical influences on decomposition and the composition and diversity of the insect communities they support. The proposed research takes advantage of natural diversity, providing an important model system at Cedar Creek.

openCC0Mar 2018View details →
zenodo28/100

Figure 1 in Comparison of the species composition of Gamasina mite communities (Acari: Mesostigmata) in selected caves of the Kraków-Cz stochowa Upland (southern Poland) and their immediate surroundings

Figure 1. Comparison of the species composition of Gamasina mite communities at the sampling sites based on Bray–Curtis distance (for abbreviations see Table 1).

opencc-by-4.0Nov 2014View details →
dryad28/100

Data from: Linking species thermal tolerance to elevational range shifts in upland dung beetles

Climate warming has been proposed as the main cause of the recent range shifts seen in many species. Although species' thermal tolerances are thought to play a key role in determining responses to climate change, especially in ectotherms, empirical evidence is still limited. We investigate the connection between species' thermal tolerances, elevational range and shifts in the lower elevational limit of dung beetle species (Coleoptera, Aphodiidea) in an upland region in the northwest of England. We measured thermal tolerances in the laboratory, and used current and historical distribution data to test specific hypotheses about the area's three dominant species, particularly the species most likely to suffer from warming: Agollinus lapponum. We found marked differences between species in their minimum and maximum thermal tolerance and in their elevational range and patterns of abundance. Overall, differences in thermal limits among species matched the abundance patterns along the elevation gradient expected if distributions were constrained by climate. A. lapponum abundance increased with elevation and this species showed lower maximum and minimum thermal limits than Acrossus depressus, for which abundance declined with elevation. Consistent with lower tolerance to high temperature, we recorded an uphill retreat of the low elevation limit of A. lapponum (177 m over 57 years) in line with the increase in summer temperature observed in the region over the same period. Moreover, this species has been replaced at low and mid-elevations by the other two warm-tolerant species (A. depressus and Agrilinus ater). Our results provide empirical evidence that species' thermal tolerance constrains elevational ranges and contributes to explain the observed responses to climate warming. A mechanistic understanding of how climate change directly affects species, such as the one presented here, will provide a robust base to inform predictions of how individual species and whole assemblages may change in the future.

opencc-zeroDec 2017View details →
zenodo28/100

FIGURES 23–26 in New species and records for the mayfly families Caenidae, Leptohyphidae and Coryphoridae (Ephemeroptera, Pannota) from Venezuelan Guayana's Uplands

FIGURES 23–26. Study sites: 23, Kaku Parú; 24, Kavanayén; 25, Mareman Parú; 26, Aponwao.

opennotspecifiedDec 2011View 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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