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Fig. 2 in Description of the tadpole and natural history notes of Incilius spiculatus (Mendelson, 1997), an Endangered toad endemic to the Sierra Madre de Oaxaca, Mexico
Fig. 2. Breeding behavior of Incilius spiculatus. (A–B) Amplexus (axillary type) and oviposition, (C) egg string staggered in unilayered tube, (D–E) dorsal and ventral views of the tadpole head at Gosner stage 24 showing the "elongated mouth," (F) Rio Coyul, San Pedro Yolox; (G) lateral view of tadpole at Gosner stage 39, and (H) lateral view of metamorphic individual.
Fig. 1 in Description of the tadpole and natural history notes of Incilius spiculatus (Mendelson, 1997), an Endangered toad endemic to the Sierra Madre de Oaxaca, Mexico
Fig. 1. Tadpole of Incilius spiculatus. (A) Oral disc at Gosner stage 37, (B) lateral view at Gosner stage 35, and (C) dorsal view at Gosner stage 35.
Fig. 6 in Discovery of a reproducing population of the Mindo Glassfrog, Nymphargus balionotus (Duellman, 1981), at the Río Manduriacu Reserve, Ecuador, with a literature review and comments on its natural history, distribution, and conservation status
Fig. 6. Nymphargus balionotus breeding behavior. (A) Calling male; (B) Male and female in amplexus; (C) Egg mass deposited on the bottom surface on a leaf. Photos by Ross J. Maynard (A) and Jaime Culebras (B–C).
Fig 5 in Discovery of a reproducing population of the Mindo Glassfrog, Nymphargus balionotus (Duellman, 1981), at the Río Manduriacu Reserve, Ecuador, with a literature review and comments on its natural history, distribution, and conservation status
Fig 5. Iris variation in Nymphargus balionotus. Photos by Jaime Culebras (A–C) and Scott Trageser (D).
Fig. 4 in Discovery of a reproducing population of the Mindo Glassfrog, Nymphargus balionotus (Duellman, 1981), at the Río Manduriacu Reserve, Ecuador, with a literature review and comments on its natural history, distribution, and conservation status
Fig. 4. Metamorphic life stage of Nymphargus balionotus; dorsal (A) and ventral (B) views (ZSFQ 3895). Photos by Ross J. Maynard.
Fig. 3 in Discovery of a reproducing population of the Mindo Glassfrog, Nymphargus balionotus (Duellman, 1981), at the Río Manduriacu Reserve, Ecuador, with a literature review and comments on its natural history, distribution, and conservation status
Fig. 3. Pattern and color variation in adult Nymphargus balionotus. (A) Male, uncollected; (B) Male, ZSFQ 0531; (C) Male, uncollected; (D) Male, uncollected; (E–F) Male, ZSFQ 0532; (G–H) Gravid female, uncollected. Photos by Ross J. Maynard.
Fig. 2 in Discovery of a reproducing population of the Mindo Glassfrog, Nymphargus balionotus (Duellman, 1981), at the Río Manduriacu Reserve, Ecuador, with a literature review and comments on its natural history, distribution, and conservation status
Fig. 2. Audio spectrogram (top), oscillogram (middle), and power spectrum (bottom) graphs of a single male Nymphargus balionotus advertisement call.
Fig. 1 in Discovery of a reproducing population of the Mindo Glassfrog, Nymphargus balionotus (Duellman, 1981), at the Río Manduriacu Reserve, Ecuador, with a literature review and comments on its natural history, distribution, and conservation status
Fig. 1. Distribution map of known localities for Nymphargus balionotus. Information tags to the left summarize data reported for each locality, including (in order): name of collection site, department/province, number of specimens reported, elevation, and year specimens were collected or observed. Blue circle represents the Río Manduriacu Reserve; red circle marks the type locality; yellow and gray circles represent remaining localities reported in the literature, with the gray (Campamento Chancos) population believed to be a distinct lineage by Cisneros-Heredia and McDiarmid (2006). Note: the "El Tambo" locality in the department of Cauca, Colombia, has been placed as accurately as possible based on available information (see Discussion).
Fig. 4 in Insights into the natural history of the endemic Harlequin Toad, Atelopus laetissimus Ruiz-Carranza, Ardila-Robayo, and Hernández-Camacho, 1994 (Anura: Bufonidae), in the Sierra Nevada de Santa Marta, Colombia
Fig. 4. Habitat suitability estimate (upper left panel), minimum convex polygon of extent of occurrence (EEO, upper right panel), and area of occupation (AOO, lower left panel) of Atelopus laetissimus. The total deforested area for the analyzed period and species occurrence locations are provided in red.
Figure 3 in Insights into the natural history of the endemic Harlequin Toad, Atelopus laetissimus Ruiz-Carranza, Ardila-Robayo, and Hernández-Camacho, 1994 (Anura: Bufonidae), in the Sierra Nevada de Santa Marta, Colombia
Figure 3. Acoustic repertoire of the advertisement call of Atelopus laetissimus. Conventional pulsed call (A), unpulsed short call (B), partially pulsed short call (C), pulsed short call (D), partially pulsed short call before pulsed call (E), and partially pulsed short call within pulsed call (F). The corresponding author will provide tables of raw data for individual specimens on request.
Fig. 2 in Insights into the natural history of the endemic Harlequin Toad, Atelopus laetissimus Ruiz-Carranza, Ardila-Robayo, and Hernández-Camacho, 1994 (Anura: Bufonidae), in the Sierra Nevada de Santa Marta, Colombia
Fig. 2. Temporal variation of the number of recaptures (A) and movement patterns (B) of Atelopus laetissimus.
Fig. 1 in Insights into the natural history of the endemic Harlequin Toad, Atelopus laetissimus Ruiz-Carranza, Ardila-Robayo, and Hernández-Camacho, 1994 (Anura: Bufonidae), in the Sierra Nevada de Santa Marta, Colombia
Fig. 1. (A) Temporal variation of relative abundance (ind/[h × obs]). (B) Population density (m2) per habitat of Atelopus laetissimus. Roman numerals represent the months of the surveys.
Fig. 5 in Insights into the natural history of the endemic Harlequin Toad, Atelopus laetissimus Ruiz-Carranza, Ardila-Robayo, and Hernández-Camacho, 1994 (Anura: Bufonidae), in the Sierra Nevada de Santa Marta, Colombia
Fig. 5. Estimated annual habitat loss for Atelopus laetissimus in the last decade in the potential distribution (A), area of occurrence (AOO, B), and extent of occurrence (EOO, C).
Fig. 4 in First field report of Trimerodytes percarinatus (Boulenger, 1899) (Reptilia: Squamata: Natricidae) from India with notes on its natural history
Fig. 4 Location of first field sighting of Trimerodytes percarinatus in Namdapha Tiger Reserve, Arunachal Pradesh, India.
Fig. 2 in First field report of Trimerodytes percarinatus (Boulenger, 1899) (Reptilia: Squamata: Natricidae) from India with notes on its natural history
Fig. 2 Comparison between right and left sides of the head of Trimerodytes percarinatus from Namdapha, India.
Fig. 13 in Notes on the natural history and morphology of the Ningshan Lined Snake (Stichophanes ningshaanensis Yuen, 1983; Ophidia: Colubridae) and its distribution in the Shennongjia National Nature Reserve, China
Fig. 13. Comparison of typical head scales and head shapes of Oligodon (top); 8 supralabials, 4 and 5 in contact with eye, 2 pre-oculars, 2 post-oculars, 1+2 temporals, 1 loreal, enlarged, upturned rostral scale, to the head scales of Stichophanes (bottom); 6 supralabials, 3 and 4 in contact with eye, 1 pre-ocular, 2 post-oculars, 1+2 temporals, no loreal, blunt rostral scale. Photos by Kevin R. Messenger.
Fig. 7 in Notes on the natural history and morphology of the Ningshan Lined Snake (Stichophanes ningshaanensis Yuen, 1983; Ophidia: Colubridae) and its distribution in the Shennongjia National Nature Reserve, China
Fig. 7. Courtship behavior by the male, rubbing his chin along the female, observed on 28 June 2006. Photo by Kevin R. Messenger.
Fig. 9. Nine eggs from a female measuring 533 in Notes on the natural history and morphology of the Ningshan Lined Snake (Stichophanes ningshaanensis Yuen, 1983; Ophidia: Colubridae) and its distribution in the Shennongjia National Nature Reserve, China
Fig. 9. Nine eggs from a female measuring 533 mm SVL and 673 mm TL on 30 June 2006. Photo by Kevin R. Messenger.
Fig. 1 in Notes on the natural history and morphology of the Ningshan Lined Snake (Stichophanes ningshaanensis Yuen, 1983; Ophidia: Colubridae) and its distribution in the Shennongjia National Nature Reserve, China
Fig. 1. Locations of field stations and of Stichophanes ningshaanensis (n = 22) within the Shennongjia NNR.
Fig. 12 in Notes on the natural history and morphology of the Ningshan Lined Snake (Stichophanes ningshaanensis Yuen, 1983; Ophidia: Colubridae) and its distribution in the Shennongjia National Nature Reserve, China
Fig. 12. Comparison of right maxillae; Oligodon on the top, with the characteristic kukri-shaped rear teeth which it uses to saw into eggs, distinguished from the anterior teeth (from Coleman et al. 1993), Stichophanes on the bottom, anterior teeth all the same, and a lack of rear-specialized teeth (from Wang et al. 2014).
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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.
Annotated Behaviour and Observability Dataset (ABODe)
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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.