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549 results for “use of habitat”
Data from: Foraging behaviour and habitat-use drives niche segregation in sibling seabird species
<p>To mediate competition, similar sympatric species are assumed to utilise different resources, or the same but geographically separated resources. The two giant petrels (<em>Macronectes</em> spp.) are intriguing in that they are morphologically similar seabirds with overlapping diets and distributions. To better understand the mechanisms allowing their co-existence, we investigated intra- and interspecific niche segregation at Marion Island (Southern Indian Ocean), one of the few localities where they breed in sympatry. We used GPS tracks from 94 individuals and remote-sensed environmental data to quantify habitat-use, combined with blood carbon and nitrogen stable isotope ratios from 90 individuals to characterise their foraging habitat and trophic ecology. Females of both species made distant at sea foraging trips and fed at a similar trophic level. However, they used distinct pelagic habitats. In contrast, males of both species mainly foraged on or near land, resulting in significant sexual segregation, but high interspecific habitat and diet overlap. However, some males showed flexible behavioural strategies, also making distant, pelagic foraging trips. Using contemporaneous tracking, environmental and stable isotope data we provide a clear example of how sympatric sibling species can be segregated along different foraging behaviour dimensions.</p>
Dataset for: African manatee (Trichechus senegalensis) habitat suitability at Lake Ossa, Cameroon using trophic state models and predictions of submerged aquatic vegetation
<p>See research article here: https://onlinelibrary.wiley.com/doi/epdf/10.1002/ece3.8202</p> <p>Aim: The present study aims at investigating the past and current trophic status of Lake Ossa and evaluating its potential impact on African manatee health.</p> <p>Location: Lake Ossa is known as a refuge for the threatened African manatees in Cameroon. Little information exists on the water quality and health of the ecosystem as reflected by its chemical and biological characteristics.</p> <p>Methods: Aquatic biotic and abiotic parameters including water clarity, nitrogen, phosphorous and chlorophyll concentrations were measured monthly during four months at each of 18 water sampling stations evenly distributed across the lake. These parameters were then compared with historical values obtained from the literature to examine the dynamic trophic state of Lake Ossa.</p> <p>Results: Results indicate that Lake Ossa’s trophic state parameters doubled in only three decades (from 1985 to 2016), moving from a mesotrophic to a eutrophic state. The decreasing nutrient gradient moving from the mouth of the lake (in the south) to the north indicates that the flow of the adjacent Sanaga River is the primary source of nutrient input. Further analysis suggests that the poor transparency of the lake is not associated with chlorophyll concentrations but rather with the suspended sediments brought-in by the Sanaga River. Consequently, our model demonstrated that despite nutrient enrichment, less than 5% of the lake bottom surface sustained submerged aquatic vegetation. Thus, shoreline emergent vegetation is the primary food available for the local manatee population. During the dry season, water recedes drastically and disconnects from the dominant shoreline emergent vegetation, decreasing accessibility for manatees.</p> <p>Main conclusions: The current study revealed major environmental concerns (eutrophication and sedimentation) that may negatively impact habitat quality for manatees. Efficient land use and water management across the entire watershed may be necessary to mitigate such issues.</p>
Fig. 1 in Natural-Licks Use By Orangutans And Conservation Of Their Habitats In Bornean Tropical Production Forest
Fig. 1. Location maps of Deramakot Forest Reserve in Sabah, Malaysian Borneo (D1 to D4: natural-licks).
Data from: Phenology of penaeid shrimp nursery habitat use: trends and environmental drivers over four decades
<p>These datasets are those used in analysis published in Batchelder et al. 2024 (for full abstract see: https://doi.org/10.3354/meps14741). </p>
Fig. 1 in The impact of land use on species composition and habitat structure in Sudanian savannas - A modelling study in protected areas and agricultural lands of southeastern Burkina Faso
Fig. 1. − Study area including the Pama reserve and neighbouring PAs of the western WAPO complex. The Pama, Tindangou and Madjoari areas are enclaves where agriculture is allowed. The small country map in the lower right shows the position of the study area within Burkina Faso.
Fig. 3 in The impact of land use on species composition and habitat structure in Sudanian savannas - A modelling study in protected areas and agricultural lands of southeastern Burkina Faso
Fig. 3. − Maps of mean maximum plant size (calculated as average of maximum plant size of all species predicted as present within a grid cell). A. Grasses (Poaceae) (30-360 cm); B. Woody species (3-25 m). The color coding stretches from light yellow for the lowest values via orange and red to violet for the highest values.
Fig. 2 in The impact of land use on species composition and habitat structure in Sudanian savannas - A modelling study in protected areas and agricultural lands of southeastern Burkina Faso
Fig. 2. − Maps of species richness. A. All plant species (2-211 spp.); B. Graminoids (0-50 spp.); C. Forbs (0-86 spp.); D. Woody species (0-52 spp.); E. Weedy species (0-48 spp.); F. Non-weedy species (0-140 spp.). The color coding stretches from light yellow for the lowest values via orange and red to violet for the highest values.
Data for: The interaction between metabolic rate, habitat choice, and resource use in a polymorphic freshwater species
<p>Raw respirometry data and respirometry code</p> <p>Data.xlsx is the data about each fish that was used for all analyses including Stable Isotope values, length, weight, sex, and habitat. This is the data that is used in the R code. </p> <p>Example code of the models used in our analyses</p> <p>TEF_metabolism.xlsx is data on the fish that were kept in the lab for almost a year. </p> <p> </p>
Habitats as predictors in species distribution models: Shall we use continuous or binary data?
<p>The representation of a land cover type (i.e., habitat) within an area is often used as an explanatory variable in species distribution models. However, it is possible that a simple binary presence/absence of the suitable habitat might be the most important determinant of the presence/absence of some species and, thus, be a better predictor of species occurrence than the continuous parameter (area). We hypothesize that the binary predictor is more suitable for relatively rare habitats (e.g., wetlands) while for common habitats (e.g., forests) the amount of the focal habitat is a better predictor. We used the Third Atlas of Breeding Birds in the Czech Republic as the source of species distribution data and CORINE Land Cover inventory as the source of the landcover information. To test our hypothesis, we fitted generalized linear models of 32 water and 32 forest bird species. Our results show that for water bird species, models using binary predictors (presence/absence of the habitat) performed better than models with continuous predictors (i.e., the amount of the habitat); for forest species, however, we observed the opposite. Thus, future studies using habitats as predictors of species occurrences should consider the prevalence of the habitat in the landscape, and the biological role of the habitat type in the particular species' life history. In addition, performing a preliminary comparison of the performance of the binary and continuous versions of habitat predictors (e.g., using information criteria) prior to modelling, during variable selection, can be beneficial. These are simple steps that will improve explanatory and predictive performance of models of species distributions in biogeography, community ecology, macroecology, and ecological conservation.</p>
Environmental nucleic acids: a field-based comparison for monitoring freshwater habitats using eDNA and eRNA
<p>Nucleic acids released by organisms and isolated from environmental substrates are increasingly being used for molecular biomonitoring. While environmental DNA (eDNA) has received attention recently, the potential of environmental RNA as a biomonitoring tool remains less explored. Several recent studies using paired DNA and RNA metabarcoding of bulk samples suggest that RNA might better reflect "metabolically active" parts of the community. However, such studies mainly capture organismal eDNA and eRNA. For larger eukaryotes, isolation of extra-organismal RNA will be important, but viability needs to be examined in a field-based setting. In this study we evaluate (a) whether extra-organismal eRNA release from macroeukaryotes can be detected given its supposedly rapid degradation, and (b) if the same field collection methods for eDNA can be applied to eRNA. We collected eDNA and eRNA from water in lakes where fish community composition is well documented, enabling a comparison between the two nucleic acids in two different seasons with monitoring using conventional methods. We found that eRNA is released from macroeukaryotes and can be filtered from water and metabarcoded in a similar manner as eDNA to reliably provide species composition information. eRNA had a small but significantly greater true positive rate than eDNA, indicating that it correctly detects more species known to exist in the lakes. Given relatively small differences between the two molecules in describing fish community composition, we conclude that if eRNA provides significant advantages in terms of lability, it is a strong candidate to add to the suite of molecular monitoring tools.</p>
Sex-based differences in the use of post-fire habitats by invasive cane toads (Rhinella marina)
<p>Wildfires can modify habitat attributes, and those changes may differentially affect males versus females within a species if there is pre-existing niche divergence between the sexes. We used radio-tracking and dissections to study invasive cane toads (<em>Rhinella marina</em>), and performed transect counts on native frogs and cane toads 12 months after extensive fires in forests of eastern Australia. Both toads and native frogs were encountered more frequently in burned sites than in unburned sites. Most microhabitat features were similar between burned versus unburned areas, but fire had differential impacts on the ecology of male versus female toads. In burned areas females were less numerous but were larger, in better body condition, and had consumed more prey (especially, coleopterans and myriapods). The impact of fire on attributes of retreat-sites (e.g., temperature, density of vegetation cover) also differed between the sexes. More generally, intraspecific divergence in ecological traits within a species (as a function of body size as well as sex) may translate into substantial divergences in the impacts of habitat change.</p>
Congruence among multiple indices of habitat preference for species facing human-induced rapid environmental change: A case study using the Brewer's sparrow
<p>Accurate evaluations of habitat preference are key to understanding optimal conditions for wildlife survival and reproduction. Habitat selection, however, usually is evaluated using a single index of preference, and congruence among multiple, relevant indices of preference is examined rarely.</p> <p>We assessed the concordance between patterns of habitat preference using three different indices of breeding site preference in a migratory songbird. Specifically, we compared the chronology of territorial establishment, pair formation, and reproductive initiation of the Brewer's sparrow (<em>Spizella breweri</em>) along a gradient of surface disturbance associated with natural gas development in Wyoming, USA during 2019.</p> <p>We expected all three indices to demonstrate a preference for breeding sites with less surface disturbance, where reproductive success typically is higher. By contrast, all indices suggested suboptimal preference with respect to surface disturbance, with some discrepancy among them. The chronology of settlement and pairing did not vary across the disturbance gradient, whereas nest initiation tended to occur earlier at sites with more disturbance.</p> <p>If the pattern of suboptimal selection of breeding sites that we identified is generalizable across other populations of migratory birds affected by energy development, the resultant lower fitness in those areas may exacerbate population declines.</p> <p>Our results suggest that traditional, single-index approaches to the study of habitat selection, if chosen carefully, may provide adequate inference on habitat preferences. Different metrics, however, can lead to at least subtle differences in patterns of habitat selection. The simultaneous examination of multiple indices of preference across a diversity of systems would help clarify the contexts under which preference metrics can become decoupled.</p>
Chronic wasting disease alters the movement behavior and habitat use of mule deer during clinical stages of infection
<p>Integrating host movement and pathogen data is a central issue in wildlife disease ecology that will allow for a better understanding of disease transmission. We examined how adult female mule deer (<em>Odocoileus hemionus</em>) responded behaviorally to infection with chronic wasting disease (CWD). We compared movement and habitat use of CWD-infected deer (<em>n</em> = 18) to those that succumbed to starvation (and were CWD-negative by ELISA and IHC; <em>n</em> = 8) and others in which CWD was not detected (<em>n</em> = 111, including animals that survived the duration of the study) using GPS collar data from two distinct populations collared in central Wyoming, USA during 2018–2022. CWD and predation were the leading causes of mortality during our study (32 of 91 deaths attributed to CWD and 27 of 91 deaths attributed to predation). Deer infected with CWD moved slower and used lower elevation areas closer to rivers in the months preceding death compared with uninfected deer that did not succumb to starvation. Although CWD-infected deer and those that died of starvation moved at similar speeds during the final months of life, CWD-infected deer used areas closer to streams with less herbaceous biomass than deer that died of starvation. These behavioral differences may allow for the development of predictive models of disease status from movement data, which will be useful to supplement field and laboratory diagnostics or when mortalities cannot be quickly retrieved to assess cause-specific mortality. Furthermore, identifying individuals that are sick before predation events could help to assess the extent to which disease mortality is compensatory with predation. Finally, infected animals began to slow down around four months prior to death from CWD. Our approach for detecting the timing of infection-induced shifts in movement behavior may be useful in application to other disease systems to better understand the response of wildlife to infectious disease.</p>
Fig. 1 in SHORT COMMUNICATION Monitoring a population of Cruziohyla craspedopus (Funkhouser, 1957) using an artificial breeding habitat
Fig. 1. Site map for ABHab points at LPS: dashed line is approximate separation of terra firma and flood plain forest.
Fig. 10 in Can artificial retreat sites help frogs recover after severe habitat devastation? Insights on the use of "coqui houses" after Hurricane Maria in Puerto Rico
Fig. 10. Comparison of the relative abundance, measured as the number of adult Eleutherodactylus coqui observed per sampling night in the experimental transect where artificial coqui houses were made available, versus the control.
Fig. 6 in Can artificial retreat sites help frogs recover after severe habitat devastation? Insights on the use of "coqui houses" after Hurricane Maria in Puerto Rico
Fig. 6. Variation in operative temperatures measured by frog agar models in typical forest microhabitats after Hurricane Maria, showing a significant decrease during the cool-dry season (in blue) during midday (A), and nighttime (B).
Fig. 8 in Can artificial retreat sites help frogs recover after severe habitat devastation? Insights on the use of "coqui houses" after Hurricane Maria in Puerto Rico
Fig. 8. Bar graphs showing coqui house occupancy rate by Eleutherodactylus coqui during the length of this study by daytime (A), and by nighttime (B) surveys. The shaded area in (A) denotes sampling in months during the cool-dry season.
Fig. 7 in Can artificial retreat sites help frogs recover after severe habitat devastation? Insights on the use of "coqui houses" after Hurricane Maria in Puerto Rico
Fig. 7. Box plots showing variation in forest microhabitat temperature by day (A) and night (B) during the cool-dry season (February) of 2015 (a non-hurricane year), and in 2019, 17 months after Hurricane Maria hit Puerto Rico.
Fig. 5 in Can artificial retreat sites help frogs recover after severe habitat devastation? Insights on the use of "coqui houses" after Hurricane Maria in Puerto Rico
Fig. 5. Drastic changes in temperature at the transects in the Palo Colorado forest of El Yunque as a consequence of Hurricane Maria. (A) Ambient temperatures registered by HOBO data logger in the forest understory before, during, and shortly after Hurricane Maria. (B–C) Box plots showing variation in forest microhabitat temperature by day and at night during the month of September in 2015 (a non-hurricane year), and in 2017, the year that Hurricane Maria hit Puerto Rico.
Fig. 2 in Can artificial retreat sites help frogs recover after severe habitat devastation? Insights on the use of "coqui houses" after Hurricane Maria in Puerto Rico
Fig. 2. Change in forest structure in the Palo Colorado forest transect (El Yunque) due to Hurricane Maria and corresponding damage/recovery stages according to Table 1. (A) Before the hurricane. (B) Same site after the hurricane, stage 1. (C) Moderate recuperation, stage 3. (D–E) Canopy dominated by Sierra Palm fronds showing signs of further recuperation of original understory vegetation, stage 4.
ScienceDex guides
Understand access before you commit
These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
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.
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.
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.
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.
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.