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.
9,097
datasets available to search
ShareScore release 0.9.0
Dataset results
9,097 results for “wild”
Fig. 3 in Maintenance of Trypanosoma cruzi, T. evansi and Leishmania spp. by domestic dogs and wild mammals in a rural settlement in Brazil-Bolivian border
Fig. 3. Path analysis on the influences of infections in relation to physical examination of dogs surveyed at Urucum settlement, Corumbá, Mato Grosso do Sul, Brazil in 2015.
Fig. 2 in Maintenance of Trypanosoma cruzi, T. evansi and Leishmania spp. by domestic dogs and wild mammals in a rural settlement in Brazil-Bolivian border
Fig. 2. Three-way Venn diagram illustrating coinfection, single infection or no infection of T. cruzi, T. evansi, and Leishmania spp. in 62 dogs from the Urucum settlement along the Brazil-Bolivia border. Total numbers and percentages are presented.
Fig. 1 in The wild world of Guinea Worms: A review of the genus Dracunculus in wildlife
Fig. 1. Life-cycle of Dracunculus insignis in wildlife and domestic dogs. Arrows in red represent transmission from (A) definitive hosts to intermediate hosts (Cyclopoid copepods) and (B) transmission to definitive hosts via consumption of intermediate hosts. Arrows in blue represent (C) transmission from intermediate hosts to paratenic and transport hosts (amphibains and fish) via consumption of infected copepods and (D) transmission to definitive hosts via consumption of paratenic/transport hosts. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
Fig. 1 in Maintenance of Trypanosoma cruzi, T. evansi and Leishmania spp. by domestic dogs and wild mammals in a rural settlement in Brazil-Bolivian border
Fig. 1. The Brazil-Bolivian border and Urucum settlement (Corumbá, MS) demonstrating the site of collections.
Fig. 3 in A comparison of helminth infections as assessed through coprological analysis and adult worm burdens in a wild host
Fig. 3. The relationship between adult lungworm (A. falciformis) burden and number of larvae per g of faeces in Irish badgers (n = 289).
Fig. 2 in A comparison of helminth infections as assessed through coprological analysis and adult worm burdens in a wild host
Fig. 2. The relationship between adult hookworm (U. criniformis) burden and faecal egg counts (e.p.g) in Irish badgers (n = 289).
Fig. 3. Seasonal detection rate for E. uekii, type B in Surveillance of Eimeria species in wild Japanese rock ptarmigans, Lagopus muta japonica, and insight into parasitic seasonal life cycle at timberline regions of the Japanese Alps
Fig. 3. Seasonal detection rate for E. uekii, type B, and mixed Eimeria spp. oocyst infection in both adults and chicks in 2006 and 2007. Numbers in parentheses below months indicate the total number of fecal samples analyzed. Data for the number of chicks (23 in 2006 and 11 in 2007) were only available for August.
Fig. 1 in Surveillance of Eimeria species in wild Japanese rock ptarmigans, Lagopus muta japonica, and insight into parasitic seasonal life cycle at timberline regions of the Japanese Alps
Fig. 1. Seasonal prevalence of Eimeria spp. infection in Japanese rock ptarmigans from April to November in 2006 and 2007. (a) and (b) show the prevalence of infection in adult birds and chicks, respectively. Numbers above bars indicate the total number of fecal samples analyzed.
Fig. 2 in Surveillance of Eimeria species in wild Japanese rock ptarmigans, Lagopus muta japonica, and insight into parasitic seasonal life cycle at timberline regions of the Japanese Alps
Fig. 2. Photomicrograph of eimerian oocysts detected in the feces of Japanese rock ptarmigans; (a) E. uekii and (b) type B. The scale bar indicates 20 μm.
Fig. 2 in Wild pigs as sentinels for hard ticks: A case study from south-central Florida
Fig. 2. Mean intensity of infestation of adult ticks collected from wild pigs from May 22, 2015 to May 09, 2017. Ticks which could not be identified to species were excluded from this figure. Values of zero indicate that wild pigs were sampled during that month, but no adults of the indicated species were collected.
Fig. 4 in Wild pigs as sentinels for hard ticks: A case study from south-central Florida
Fig. 4. Estimated mean density of host-seeking ticks per 10 m 2 by life stage and habitat type with 95% confidence intervals shown as vertical bars. Numerical values for the estimated mean densities and 95% confidence intervals are reported in Table S5.
Fig. 1 in Wild pigs as sentinels for hard ticks: A case study from south-central Florida
Fig. 1. Location of Buck Island Ranch, Lake Placid, Florida denoted by blue circle. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)
Fig. 3 in Wild pigs as sentinels for hard ticks: A case study from south-central Florida
Fig. 3. Average density of adults collected by dragging from May 14, 2015 to August 29, 2017. Values of zero indicate that drags were conducted during that month in the specified habitat, but no adults of the indicated species were collected. Symbol colors denote habitat and symbol shapes denote tick species. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)
Fig. 6 in Surveillance of Eimeria species in wild Japanese rock ptarmigans, Lagopus muta japonica, and insight into parasitic seasonal life cycle at timberline regions of the Japanese Alps
Fig. 6. Average monthly environmental temperatures on the windward and leeward slopes of Mt. Tateyama from 2006 to 2007. The temperatures on the windward slopes were not measured in April. The table below the graph shows monthly maximum and minimum temperatures.
Fig. 5 in Surveillance of Eimeria species in wild Japanese rock ptarmigans, Lagopus muta japonica, and insight into parasitic seasonal life cycle at timberline regions of the Japanese Alps
Fig. 5. Sporulation rate for Eimeria spp. (mainly E. uekii) after incubation at different temperatures for 48 h. Dark bars indicate sporulation rates of> 85% after incubation for 24 h.
Fig. 2 in Microclimate and host body condition influence mite population growth in a wild bird-ectoparasite system
Fig. 2. Distribution of nest mite population sizes estimated when nests were placed in a Berlese funnel after nestlings had fledged. All nests began the experiment with the same population size (100 live mites), mimicking identical transmission, but ending population sizes 30–35 days later were highly variable. This suggests that factors of the nest environment or hosts may be playing an important role in mite population growth.
Fig. 4 in Microclimate and host body condition influence mite population growth in a wild bird-ectoparasite system
Fig. 4. The relationship between the substrate the nest was built on: concrete, metal, or wood (y-axis) and the number of mites estimated in the field when chicks were 12 days old. Nests built on wooden substrates had significantly more mites compared to nests built on concrete or metal substrates. This graph was made using raw data, but models reported in the text included site as a random effect.
Fig. 3 in Microclimate and host body condition influence mite population growth in a wild bird-ectoparasite system
Fig. 3. Relationship between the number of non-mite arthropods (x-axis) and nest mites (y-axis) that were recovered when experimental nests were removed from the field after nestlings fledged and placed in a Berlese funnel. Nests with more arthropods had significantly fewer nest mites. This graph was made using raw data, but models reported in text had a Poisson distribution and included site as a random effect.
Fig. 2 in Prevalence of Capillaria plica in Danish wild carnivores
Fig. 2. The prevalence of Capillaria plica infections in red foxes per region of Denmark (positive red foxes/total number of red foxes examined). The origin of five red foxes was unknown.
Fig. 1. A in Prevalence of Capillaria plica in Danish wild carnivores
Fig. 1. A typical barrel-shaped Capillaria plica egg in urine sediment from a red fox. The egg show a slightly pitted shell and two opercules with polar plugs. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
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.