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”
Figure 1 in Application of multifactorial discriminant analysis in the morphostructural differentiation of wild and cultured populations of Vieja Azul (Andinoacara rivulatus)
Figure 1. (a) Location of 25 anatomic landmark points designed on the left-side view of Andinoacara rivulatus; (b) 32 truss characters making up a truss network. 1- Commissure of the mouth; 2- most cranial point of the upper premaxilla; 3- origin of pelvic fin; 4- origin of dorsal fin; 5- origin of anal fin; 6- most cranial point of the base of the tenth spine of the dorsal fin; 7- ending of anal fin; 8- ending of dorsal fin; 9- ventral origin of caudal fin; 10- dorsal origin of caudal fin; 11- most cranial point of caudal peduncle; 12- most caudal point of caudal peduncle; 13- ending of pectoral fin; 14- end of operculum; 15- cranial edge of the eye; 16- caudal edge of the eye; 17- preoccipital (most posterior aspect of neurocranium); 18- below operculum; 19- origin of pectoral fin; 20- lower end of the head; 21- anal opening; 22- most cranial point of the lower premaxilla; 23- ending of 1st dorsal fin ray; 24- ending of the last anal fin ray; 25- ending of the pelvic fin radius.
Figure S1 in Do Castanea sativa wild provenances influence Dryocosmus kuriphilus Yasumatsu (Hymenoptera: Cynipidae) infestations?
Figure S1. Results of climatic data analysis of the interval June–July (left panel a) and December–February (right panel b) in 2013, 2014, 2015, and 2016. Temperature and relative humidity indicate mean value (dot) and standard error (bars). Rain is the sum of total rainfall in the interval, without confidence interval. The left vertical axis is divided in two sections, the average temperature at bottom, and the relative humidity at the top, respectively. Different letters indicate significant differences between years at p <0.05. Differences between years in temperature and relative humidity were tested with ANOVA and posthoc Tukey HSD test (p <0.05). Difference in rainfall between years were tested with x!-test (p <0.05).
Figure 3 in Do Castanea sativa wild provenances influence Dryocosmus kuriphilus Yasumatsu (Hymenoptera: Cynipidae) infestations?
Figure 3. Infestation by D. kuriphilus on six C. sativa provenances grown in common garden field trial, during the years 2015 (top plots) and 2016 (bottom plots). Panels a) and c) number of gallsper shoot/branch; b) and d) number of cells per gall. Bars represent mean and standard error. Within each plot, different letters indicate significant difference between provenances after Bonferroni posthoc test at p <0.05.
Figure 1 in Do Castanea sativa wild provenances influence Dryocosmus kuriphilus Yasumatsu (Hymenoptera: Cynipidae) infestations?
Figure 1. South Europe map localising the experimental site in Castel Giorgio (Italy) (black dot) where the investigation was conducted. Black stars and codes identify the provenance areas of the chestnuts that were considered in this study.
Fig. 3 in Effects of latitude, host body size, and host trophic guild on patterns of diversity of helminths associated with humans, wild and domestic mammals of Mexico
Fig. 3. Phylogenetic generalized least squares (PGLS) regression of host body mass (values were log-transformed) with richness of helminths associated to wildlife hosts (values were corrected for sampling effort).
Fig. 3 in Detection of haemosporidian parasites in wild and domestic birds in northern and central provinces of Iran: Introduction of new lineages and hosts
Fig. 3. Median joining haplotype network of Haemoproteus lineages. Detected sequences in this study are in bold.
Fig. 2. Bayesian tree reconstructed using 478 in Detection of haemosporidian parasites in wild and domestic birds in northern and central provinces of Iran: Introduction of new lineages and hosts
Fig. 2. Bayesian tree reconstructed using 478-bp mitochondrial cytb gene for avian blood parasites lineages. The amplified sequences in the current study are highlighted in bold. Posterior probability support of>0.8 is displayed for each branch. Schematic tree is summarized in section A and separated clade for each genus is given in sections of B (Plasmodium), C (Haemoproteus), and D (Leucocytozoon).
Fig. 2 in Effects of latitude, host body size, and host trophic guild on patterns of diversity of helminths associated with humans, wild and domestic mammals of Mexico
Fig. 2. Relationships between latitude and the average taxonomic distinctness of overall helminths (A) and nematodes (B).
Fig. 4 in Effects of latitude, host body size, and host trophic guild on patterns of diversity of helminths associated with humans, wild and domestic mammals of Mexico
Fig. 4. Parasite richness and average taxonomic distinctness by host trophic guild (the size of circle represents the number of hosts belonging to each trophic guild).
Fig. 1 in Effects of latitude, host body size, and host trophic guild on patterns of diversity of helminths associated with humans, wild and domestic mammals of Mexico
Fig. 1. Maps showing the geographic locations of the records, classified by phylum of the subsetted database.
Fig. 3 in Molecular identification of Taenia hydatigena and Mesocestoides species based on copro-DNA analysis of wild carnivores in Mongolia
Fig. 3. Phylogenetic tree based on a partial sequence of tapeworms obtained by the maximum likelihood method was conducted using the HKY + G + I nucleotide substitution model. Numbers above branches are percent bootstrap values based on 1,000 replicates. Bootstrap value> 70% are shown. (a) Phylogenetic tree based on the cox1 sequences of T. hydatigenaand Mesocestoides sp. isolates available in the GenBankṜ database were included. Hymenolepis nana served as an out-group. (b) Phylogenetic analysis of the 12SrRNA partial sequence of T. hydatigena, Mesocestoides sp., and M. lineatus inferred using the sequence distance method and maximum likelihood. Hymenolepis nana was used as an out-group.
Fig. 1 in Molecular identification of Taenia hydatigena and Mesocestoides species based on copro-DNA analysis of wild carnivores in Mongolia
Fig. 1. Map of Mongolia showing the distribution of Taenia hydatigena (pentangle), Mesocestoides sp.-1 (square), and Mesocestoides sp.-2 (circle) by province detected by molecular identification of fecal samples from wild carnivores. Mongolia consists of 21 provinces: Arkhangai (Akh), Bayankhongor (Bkh), Bayan-Ulgii (BU), Bulgan (BG), Darkhan-Uul (DU), Dornogobi (DoG), Dundgobi (DuG), Govi-Altai (GA), Khentii (KhE), Khovd (KhO), Khuvsgul (KhU), Orkhon-Uul (OU), Selenge (SE), Sukhbaatar (SB), Tuv (TU), Umnu-Gobi (UG), Uvs (Uv), Uvurkhangai (Ukh), Zavkhan (ZKh), Dornod (D), and Gobi-Sumber (GS). The field survey was conducted in all provinces, unless Dornod (D), and GS (Gobi-Sumber). Ulaanbaatar (U) is the capital city of Mongolia. The field survey was conducted in all provinces, unless Dornod (D), and GS (Gobi-Sumber). Ulaanbaatar (U) is the capital city of Mongolia located in Tuv Province.
Fig. 2 in Toxoplasma gondii infection in European mouflons (Ovis musimon) and captive wild felines from Puebla, M�exico
Fig. 2. Representative PCR-RFLP pattern of T. gondii for SAG3 gene. Single and mixed infections in lions and mouflons tissues were observed. A. PCR for the SAG3 locus of lion 1 (L1, spleen), mouflon 1 (M1, brain) and mouflon 2 (M2, liver) samples. B. A triple infection is highlighted (yellow box). Resulting genotypes are specified at the bottom. In silico digestion was done by www.benchling.com. Reference strains sequences GT1, TGGT1_308020; Me49, TGME49_308020; VEG, TGVEG_308020 are available at www.toxodb.org. MW: molecular weight marker; RH and ME49 are reference strains, type I and II, respectively; M: mouflon, L: lion. (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 Toxoplasma gondii infection in European mouflons (Ovis musimon) and captive wild felines from Puebla, M�exico
Fig. 1. Toxoplasma gondii infection in captive mouflons in 2011 and 2012. A. Anti-T. gondii frequency distribution in fifty-five sera of mouflons sampled in 2011; black arrows indicate positive samples as determined by their position to the right of the normally distributed values of the left population. B. One year later, 41/55 original mouflons were captured, bled, and re-tested for antibodies against this parasite. The cut-off point used was 1.0 RI (dotted lines), which separated the negative population (left) from the positive cases. C. Three mouflons remained positive, five became negative, and four seroconverted positive in 2012 (red, green and blue dots, respectively); one mouflon is on the cut-off (orange dot). D. Immunohistochemistry for T. gondii in tissues from in the spleen of mouflon 1, where an immunopositive cumulus of tachyzoites can be seen (blue arrow). The nuclei of resident lymphocytes and dendritic cells were contrasted with Meyer's hematoxylin. Bar: 50 μm. R = Pearson correlation. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
Fig. 2 in Gastrointestinal and cardiorespiratory endoparasites in the wild felid guigna (Leopardus guigna) in Chile: Richness increases with latitude and first records for the host species
Fig. 2. Parasites recovered from analyzed guignas in Chile: A-anterior extremity of female Molineus sp. (40x); B- caudal extremity of female Molineus sp. with caudal spine (40x); C- oral extremity of female Angiostrongylus sp. (40x); D-lateral view of caudal extremity of female Angiostrongylus sp. (40x); E-caudal extremity of male Angiostrongylus sp., caudal bursa and spicules can be observed (40x); F- lateral view of the rounded caudal extremity of female Oslerus sp. (40x); G-lateral view of the caudal extremity of male Oslerus sp., with characteristic short and stout spicules (40x); H- oral extremity of female Troglostrongylus sp. (100x); I- lateral view of the caudal extremity of male Troglostrongylus sp., long spicules and caudal bursa can be observed (40x).
Fig. 3 in Gastrointestinal and cardiorespiratory endoparasites in the wild felid guigna (Leopardus guigna) in Chile: Richness increases with latitude and first records for the host species
Fig. 3. Parasite richness (number of species/genera) in the analyzed guignas from Chile (a) overall, (b) by geographic zone and (c) by sex. Error bars represent standard error of 5%.
Fig. 1 in Gastrointestinal and cardiorespiratory endoparasites in the wild felid guigna (Leopardus guigna) in Chile: Richness increases with latitude and first records for the host species
Fig. 1. Geographical locations and parasitism status of analyzed guigna samples in Chile. Dotted line boxes delimit the two geographic zones (Center, South) studied in Chile.
Fig. 6 in Gastrointestinal and cardiorespiratory endoparasites in the wild felid guigna (Leopardus guigna) in Chile: Richness increases with latitude and first records for the host species
Fig. 6. Distribution of parasite infection intensity (total number of helminths per guigna) in the analyzed guignas from Chile.
Fig. 1 in Cardiopulmonary nematodes of wild carnivores from Denmark: Do they serve as reservoir hosts for infections in domestic animals?
Fig. 1. Map of Denmark showing Denmark's position in Europe and a map of Denmark showing the regional division and the four major cities.
Fig. 4 in Gastrointestinal and cardiorespiratory endoparasites in the wild felid guigna (Leopardus guigna) in Chile: Richness increases with latitude and first records for the host species
Fig. 4. Richness of gastrointestinal parasites in guignas from Chile, compared (a) by geographic zone and (b) by sex. p values show the statistical significance in the Mann-Whitney U test between (a) center-south and (b) females-males.
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.