Find research datasets worth reusing
Search datasets from major research repositories and use ShareScore to quickly assess how well each record supports discovery, access, and reuse.
549
datasets available to search
ShareScore release 0.9.0
Dataset results
549 results for “use of habitat”
Fig. 3 in Seasonal, Lunar and Tidal Influences on Habitat Use of Indo-Pacific Humpback Dolphins in Beibu Gulf, China.
Fig. 3. Map of humpback dolphin sightings based on (a) dry and wet seasons, (b) lunar phases and (c) tidal phases for the humpback dolphins in northern Beibu Gulf.
Fig. 4 in Seasonal, Lunar and Tidal Influences on Habitat Use of Indo-Pacific Humpback Dolphins in Beibu Gulf, China.
Fig. 4. The profile of distance from estuary (a) and water depth (b) of humpback dolphin sightings in northern Beibu Gulf among different seasons, lunar phases and tidal phases, and significance tests (c, d). Note: "*" indicates a significance at P <0.05, "**" indicates a significance at P <0.01.
Fig. 2 in Seasonal, Lunar and Tidal Influences on Habitat Use of Indo-Pacific Humpback Dolphins in Beibu Gulf, China.
Fig. 2. Definitions for high and low tidal phases in the Beibu Gulf, China, as used in the present study.
Fig. 6 in Habitat Use and Migratory Life History of Salangid Icefish (Salangidae) Revealed by Otolith Sr/Ca Ratios
Fig. 6. Icefish (Salanx ariakensis) collected from the Yangtze River estuary show diverse otolith Sr/Ca profiles that represent whole-life residence in the sea (a), the movement from the river to the sea at during juvenile stage (b) and the movement from the sea to the river at adult stage (c).
Fig. 5 in Habitat Use and Migratory Life History of Salangid Icefish (Salangidae) Revealed by Otolith Sr/Ca Ratios
Fig. 5. Icefish (Neosalanx anderssoni) collected from Qinhuangdao (Bohai Sea) display variably high otolith Sr/Ca ratios, indicating marine residence for the fish.
Fig. 4 in Habitat Use and Migratory Life History of Salangid Icefish (Salangidae) Revealed by Otolith Sr/Ca Ratios
Fig. 4. Icefish (Neosalanx tangkahkeii) collected from the Pearl River estuary display consistently high otolith Sr/Ca ratios, indicating brackish and marine residence for these 10 fish.
Fig. 2 in Habitat Use and Migratory Life History of Salangid Icefish (Salangidae) Revealed by Otolith Sr/Ca Ratios
Fig. 2. Otolith of the icefish (Neosalanx anderssoni) collected in Qinhuangdao (Bohai Sea) showing the daily growth increments and electron microprobe transect from the core to the edge for measuring Sr/Ca ratios. Arrows point out the rectangular beam marks after the analysis by the eletron microprobe.
Fig. 1 in Habitat Use and Migratory Life History of Salangid Icefish (Salangidae) Revealed by Otolith Sr/Ca Ratios
Fig. 1. Approximate sampling locations (indicated by the arrows) of the icefish in the Bohai Sea, the Yangtze River estuary, Taihu Lake and the Pearl River estuary.
Fig. 3 in Habitat Use and Migratory Life History of Salangid Icefish (Salangidae) Revealed by Otolith Sr/Ca Ratios
Fig. 3. Consistently low otolith Sr/Ca ratios of the icefish, Neosalanx tangkahkeii (a) and, Protosalanx chinensis (b) collected from Taihu Lake and Protosalanx chinensis (c) collected from the Yangtze River estuary.
Fig. 7. A in Habitat Use and Migratory Life History of Salangid Icefish (Salangidae) Revealed by Otolith Sr/Ca Ratios
Fig. 7. A diagram shows the habitat use and migratory life history of the icefish species reconstructed from their otolith Sr/ Ca profiles.
Fig. 3 in New record of a blood-feeding terrestrial leech, Haemadipsa rjukjuana Oka, 1910 (Haemadipsidae, Arhynchobdellida) on Heuksando Island and possible habitat estimation in the current and future Korean Peninsula using a Maxent model
Fig. 3. Current (A and F) and future distribution models (B-E, G-J) for Haemadipsa rjukjuana in Korea. Dark gray represents over 0.5 MaxEnt value (suitable habitat) and light gray represents below 0.5 (unsuitable habitat). A is projected to the current climate conditions (2020), and F was built with the restricted spatial area between Heuksando Island and Gageodo Island. B-E are projections of the Maxent model to SSP585 of GISS-E2-1 climate scenarios by NASA and G-J were SSP585 of INM-CM4-8 scenarios by The Institute of Numerical Mathematics. B-E and G-J are respectively 2040, 2060, 2080, and 2100.
Fig. 2 in New record of a blood-feeding terrestrial leech, Haemadipsa rjukjuana Oka, 1910 (Haemadipsidae, Arhynchobdellida) on Heuksando Island and possible habitat estimation in the current and future Korean Peninsula using a Maxent model
Fig. 2. Projection of MaxEnt Haemadipsa rjukjuana distribution model from Heuksando Island and Gageodo Island to the current climate condition of South Korea. Red color (lower value) represents less suitable habitats and blue (higher value close to 1.0) represents suitable habitats for H. rjukjuana.
Fig. 1 in New record of a blood-feeding terrestrial leech, Haemadipsa rjukjuana Oka, 1910 (Haemadipsidae, Arhynchobdellida) on Heuksando Island and possible habitat estimation in the current and future Korean Peninsula using a Maxent model
Fig. 1. The map of study sites (inset) and the Korean Peninsula. Haemadipsa rjukjuana was identified from the regions shaded in gray.
Figure 2 in Carbon primary sources and estuarine habitat use by two congeneric ariid catfishes in a subtropical coastal lagoon
Figure 2. Carbon isotope ratios (d13C) and total length (TL, mm) of individuals of Genidens genidens (closed circles) and Genidens barbus (open circles) collected in the interface between the estuarine and freshwater zones of Patos Lagoon in present study. DISCUSSION According to the model of the life cycle suggested by ARAúJO (1988), G. barbus move between freshwater to the estuary during their first year of life. After reaching sexual maturity, adults migrate to the ocean, returning to freshwater to spawn. Our work with stable isotopes corroborates the general movement pattern proposed in this model by providing evidence that the primary producers at the estuary are an important source of carbon for juveniles of G. barbus during the initial phase of their development. There is no current model describing the life cycle of G. genidens at the Patos Lagoon. ARAúJO (1988) mentioned that this species remains in the upper limit of the estuarine zone or in the limnetic portion of the lagoon and that its juveniles are occasionally found in the estuary. Based on fish sampling restricted to the mixohaline zone of the Patos Lagoon, some authors classified this species as estuarine resident (CHAO et al. 1985, ARAúJO 1988). However, VIEIRA et al. (2010) demonstrated that G. genidens occurs from the estuary to the uppermost northern portion of the lagoon, which is located ~180 km from the lagoon's connection with the sea, and can remain year round at freshwater. Our work provides new evidence that this catfish species derives energy from the estuarine and freshwater zones of
Fig. 5. Native plant hosting M in Distribution, habitat use and plant associations of Moluchia brevipennis (Saussure, 1864) (Blattodea: Ectobiidae): an endemic cockroach from Chilean Mediterranean Matorral biome
Fig. 5. Native plant hosting M. brevipennis cockroaches at our study site. (A) Cockroaches feeding pollen from Oenothera acaulis (Onagraceae) flowers, (B) Puya venusta (Bromeliaceae) inflorescences with cockroaches reaching nectar sources, (C) Carpobrotus chilensis (Aizoaceae) with cockroach inside inflorescence and climbing branch, (D) Haplopappus chrysantemifolius (Asteraceae) with adult and nymphs feeding on florets from floral head, black bar indicates a 1 cm scale.
Fig. 2 in Distribution, habitat use and plant associations of Moluchia brevipennis (Saussure, 1864) (Blattodea: Ectobiidae): an endemic cockroach from Chilean Mediterranean Matorral biome
Fig. 2. Distribution of sampled sites at Los Molles. Right panel show South America map highlighting central Los Molles locality in Chile's Mediterranean Matorral area. Left panel correspond to a detailed map of Los Molles showing sampling details. Black dots correspond to active collecting and gray dots to trapping, see Table 1 for more details.
Figure 3 in Diet and habitat use of the endangered Persian leopard (Panthera pardus saxicolor) in northeastern Iran*
Figure 3. Leopard distribution map (based on direct observation, scat, track, and prey carcass locations) and habitat overlap of the leopard with wild pig (Sus scrofa), porcupine (Hystrix indica), wild goat (Capra aegagrus), wild sheep (Ovis orientalis), and pika (Ochotona rufescens) in SNP.
Figure 1 in Using of fluctuating asymmetry in adult Pelophylax ridibundus (Amphibia: Anura: Ranidae) meristic traits as a method for assessing developmental stability of population and environmental quality of their habitat: industrial area in southern Bulgaria
Figure 1. An indicative map of the sites in southern Bulgaria where P. ridibundus individuals were captured in 2019.
Figure 2 in Using of fluctuating asymmetry in adult Pelophylax ridibundus (Amphibia: Anura: Ranidae) meristic traits as a method for assessing developmental stability of population and environmental quality of their habitat: industrial area in southern Bulgaria
Figure 2. Photos of some asymmetric P. ridibundus individuals from site 1: the Chaya River in southern Bulgaria. Legend: a–d: asymmetric morphological traits on the back of the body and hind limbs of frogs, e–f: asymmetric morphological traits on the fingers of frogs. Trait 1 – number of stripes on the dorsal side of the thigh (femur); trait 2 – number of spots on the dorsal side of the thigh; trait 3 – number of stripes on the dorsal side of the shank (crus); trait 4 – number of spots on the dorsal side of the shank; trait 5 – number of stripes on the foot (pes); trait 6 – number of spots on the foot; trait 7 – number of stripes and spots on the back (dorsum); trait 8 – number of white spots on the ventral side of the second finger of the hind leg; trait 9 – number of white spots on the ventral side of the third finger of the hind leg; trait 10 – number of white spots on the ventral side of the fourth finger of the hind leg.
Fig. 2 in Use Of Intertidal Mangrove And Sea Wall Habitats By Coral Reef Fishes In The Wakatobi Marine Park, Indonesia
Fig. 2. Number of species seen at the two intertidal sites, and the number showing low (<33%), medium (33-67%) and high (>67%) site-fidelity
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.