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Fig. 3 in Activity patterns of frugivorous phyllostomid bats in an urban fragment in southwest Amazonia, Brazil
Fig. 3. Number of captures of the four most abundant species, according to the rainfall in the ParQue Zoobotânico, Rio Branco, state of Acre, northern Brazil.
Fig. 2 in Activity patterns of frugivorous phyllostomid bats in an urban fragment in southwest Amazonia, Brazil
Fig. 2. Number of captures of the four most abundant species throughout the night period, according to hours after sunset, in the ParQue Zoobotânico, Rio Branco, state of Acre, northern Brazil.
Fig. 1 in Activity patterns of frugivorous phyllostomid bats in an urban fragment in southwest Amazonia, Brazil
Fig. 1. Location of the forest fragment (ParQue Zoobotânico) in the urban area of Rio Branco, Acre, southwestern Amazonia, Brazil.
Fig. 1 in Bird diversity in an urban ecosystem: the role of local habitats in understanding the effects of urbanization
Fig. 1. Bird species richness and overall abundance recorded in point counts (surveyed on September 2013) in the municipality of Canoas, Rio Grande do Sul, Brazil.
Fig. 2 in Bird diversity in an urban ecosystem: the role of local habitats in understanding the effects of urbanization
Fig. 2. Ordination diagram presenting the first two axes of the Canonical Correspondence Analysis (CCA) (percent of explained variability: axis I = 7.1%, axis II = 1.9%) based on the distribution of species abundance in 118 sample units (dots) in the urban area of Canoas, Rio Grande do Sul, Brazil, and its correlation with seven explanatory variables (arrows). The first axis shows the urbanization gradient (negatives values on left = more urbanized regions; positive values on right = less urbanized regions). All axes were significant (Monte Carlo test with 9,999 permutations: P <0.001). Species names are given in full in Appendix 1. Variables are described in Tab. I.
Fig. 6 in Gastro-intestinal parasites of urban rhesus macaques (Macaca mulatta) in the Kathmandu Valley, Nepal
Fig. 6. The prevalence of parasites is examined in relation to a) location and b) season. Multicolor triangles and circles in the plots represent individual data points (triangles) and centroid of each specific grouping factor (circle).
Fig. 3 in Gastro-intestinal parasites of urban rhesus macaques (Macaca mulatta) in the Kathmandu Valley, Nepal
Fig. 3. Photomicrographs of various GI parasites of the rhesus macaques at 400×: Trophozoite of E. histolytica (A), Cyst of E. histolytica (B), Cyst of E. coli (C), Cyst of Iodomoeba butschlii (D), Cyst of Giardia spp. (E), Trophozoite of Balantioides coli (F), Cyst of Balantioides coli (G), Egg of Trichuris spp. (H), Egg of Strongyloides spp. (I), Larva of Strongyloides spp. (J), Egg of Hookworm (K), Egg of Trichostrongylus spp. (L), Egg of Ascarid spp. (M), Egg of Physaloptera spp. (N), Egg of Toxocara spp.(O), Egg of Toxocara spp. (P), Egg of Strongyle spp. (Q), Egg of Strongyle spp.(R), Oocyst of Cryptosporidium spp. (S), Unknown spp. 1 (T).
Fig. 1 in Gastro-intestinal parasites of urban rhesus macaques (Macaca mulatta) in the Kathmandu Valley, Nepal
Fig. 1. Map showing the four fecal collection sites of the urban rhesus macaques in the Kathmandu Valley.
Fig. 2 in A single Haemoproteus plataleae haplotype is widespread in white ibis (Eudocimus albus) from urban and rural sites in southern Florida
Fig. 2. Typical Haemoproteus plataleae stages from three infected white ibis (Eudocimus alba) from South Florida. All ibis were genetically confirmed to be infected with the EUDRUB01 lineage. A-E, an ibis from Juno Beach urban park; F, an ibis from Indian Creek urban park; and G-L, an ibis from the Solid Waste site. The latter bird had rare round forms (K-L), which were absent from other H. plataleae-infected ibis. Younger stages (C, H, I) had a an evident 'cleft' between the gametocyote and erythrocyte nucleus.
Fig. 3 in A single Haemoproteus plataleae haplotype is widespread in white ibis (Eudocimus albus) from urban and rural sites in southern Florida
Fig. 3. Phylogenetic relationship of Haemoproteus plataleae from white ibis (Eudocimus albus) with other Haemoproteus spp.
Fig. 1 in A single Haemoproteus plataleae haplotype is widespread in white ibis (Eudocimus albus) from urban and rural sites in southern Florida
Fig. 1. Box plots of parasitemia values of Haemoproteus plataleae in white ibis (Eudocimus albus) sampled from South Florida from 2010 to 2022 by year (A.), season (B.), and age (C. and D.). C. shows all ibis with general adult vs. juvenile age class designations and D. shows data for the subset of ibis that were aged to specific year for juveniles (1, 2, or 3 yrs old). Years 2015 and 2017 were significantly different from each other, but both were similar to other years. For remaining figures, factors that are differently colored are significantly different from each other. Note that the x-axis maximum varies between plots.
Fig. 3 in Effect of urbanization on zoonotic gastrointestinal parasite prevalence in endemic toque macaque (Macaca sinica) from different climatic zones in Sri Lanka
Fig. 3. GI parasite genera types identified from fecal samples of toque macaques. I. Protozoan types: (A) Balantidium cyst, (B) Balantidium trophozoite, (C) Endolimax cyst, (D) Entamoeba cyst, (E) Isospora cyst. (F) Unidentified protozoan cyst; II. Cestode types: (G) Bertiella ova, (H) Diphyllobothrium ova, (I) Hymenolepis ova; III. Trematode types: (J–K) Unidentified trematode ova; IV. Acanthocephalan type: (L) Moniliformis ova; V. Nematode types: (M) Oesophagostomum ova, (N) Strongyloides ova, (O) Ascaris ova, (P) Trichuris ova, (Q) Strongyle/ Hookworm ova, (R) Enterobius ova, (S)Trichostrongylus ova, (T) Unidentified nematode ova.
Fig. 2 in Effect of urbanization on zoonotic gastrointestinal parasite prevalence in endemic toque macaque (Macaca sinica) from different climatic zones in Sri Lanka
Fig. 2. Map of Sri Lanka with sampling localities in the dry and the wet zones and the montane region.
Fig. 4 in Effect of urbanization on zoonotic gastrointestinal parasite prevalence in endemic toque macaque (Macaca sinica) from different climatic zones in Sri Lanka
Fig. 4. Number of parasite genera types (species richness) infecting M. s. aurifrons, M. s. sinica and M. s. opisthomelas in urban, suburban, and wild habitats.
Fig. 1 in Effect of urbanization on zoonotic gastrointestinal parasite prevalence in endemic toque macaque (Macaca sinica) from different climatic zones in Sri Lanka
Fig. 1. The three subspecies of macaque's endemic to Sri Lanka. (A) Common macaque (Macaca sinica sinica), (B) dusky or pale-fronted macaque (M. s. aurifrons), and (C) hill-zone macaque (M. s. opisthomelas) (image courtesy: Madura De Silva).
Fig. 5 in Urban biodiversity: Cuterebriasis in free-ranging Robinson's mouse opossum (Marmosa robinsoni) in the suburbs of Barranquilla, Colombia
Fig. 5. Second instar of Cuterebra sp. from M. robinsoni. Note the body spines appear evenly distributed in the larva's body.
Fig. 4 in Urban biodiversity: Cuterebriasis in free-ranging Robinson's mouse opossum (Marmosa robinsoni) in the suburbs of Barranquilla, Colombia
Fig. 4. Development stages of Cuterebra sp. found in different hosts of M. robinsoni. A. Second instar. B. Third instar.
Fig. 2 in Urban biodiversity: Cuterebriasis in free-ranging Robinson's mouse opossum (Marmosa robinsoni) in the suburbs of Barranquilla, Colombia
Fig. 2. Primers used to amplify and sequence the mitochondrial cytochrome Oxidase subunit I gene (COX1) of Cuterebra sp. List of primers: Droso-mt1490 5′- TTTCWACWAATCATAAAGATATYGG-3′, Droso-mt1729 5′-GGAGCYCCTGAYATRGCATTYCC-3′, Droso-mt1819 5′-GTRCCAGCYCCRTTTTCTAC-3′, Droso-mt2162 5′- CAACATTTATTYTGATTYTTTGG-3′, Droso-mt2169 5′-TAAACTTCAGGRTGWCCAAARAATCA-3′ y Droso-mt2680 5′-GYTAATCCWGTAAATAAWGG-3′.
Fig. 1 in Urban biodiversity: Cuterebriasis in free-ranging Robinson's mouse opossum (Marmosa robinsoni) in the suburbs of Barranquilla, Colombia
Fig. 1. Map of the Atlantic department of Colombia showing the four areas (red dots) of study of M. robinsoni: Palomar, Carreto, Luriza, and Zona Franca Celsia (visualized with Google Earth Pro). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
Fig. 3. Free range M. robinsoni with interscapular wounds. A in Urban biodiversity: Cuterebriasis in free-ranging Robinson's mouse opossum (Marmosa robinsoni) in the suburbs of Barranquilla, Colombia
Fig. 3. Free range M. robinsoni with interscapular wounds. A. External appearance of bot fly larva wound. B. Extraction of Cuterebra sp. larvae.
ScienceDex guides
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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.