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338 results for “geographic range”
Fig. 1 in Consistency in fruit preferences across the geographical range of the frugivorous bats Artibeus, Carollia and Sturnira (Chiroptera)
Fig. 1. Number of records for the four fruit genera most frequently consumed by Artibeus, Carollia and Sturnira (total number of records for each bat species) based on literature review.
Fig. 6 in Expanding the geographic and geochronologic range of early pinnipeds: New specimens of Enaliarctos from Northern California and Oregon
Fig. 6. Mandibles and vertebrae of pinniped mammal Enaliarctos sp. (UWBM 89114) from Moolack Beach, Lincoln County, Oregon, Astoria Formation, late early Miocene. Two sides of the block (A, B). Photographs (A1, B1), explanatory drawings (A2, B2). Abbreviations: CV, cervical vertebra; TV, thoracic vertebra.
Fig. 1 in Expanding the geographic and geochronologic range of early pinnipeds: New specimens of Enaliarctos from Northern California and Oregon
Fig. 1. Locality map for fossils of enaliarctines. Map of Oregon and California (A), the coastline near Newport, Oregon (B), the coastline near Point Arena, California (C).
Fig. 3 in Expanding the geographic and geochronologic range of early pinnipeds: New specimens of Enaliarctos from Northern California and Oregon
Fig. 3. Mandible of pinniped mammal Enaliarctos mealsi (UCMP 114474) from Schooner Gulch, Mendocino County, California, earliest Miocene; in lingual (A), occlusal (B), and labial (C) views.
Fig. 5 in Expanding the geographic and geochronologic range of early pinnipeds: New specimens of Enaliarctos from Northern California and Oregon
Fig. 5. Elements of pinniped mammal Enaliarctos sp., cf. E. tedfordi Berta, 1991 (UCMP 253400) from Ona Beach, Lincoln County, Oregon, Yaquina Formation, early late Oligocene; overview of original block (A), lingual (B), occlusal (C), and labial (D) views; matrix preserving impression of lingual side of p4 and m1 (E).
Fig. 8 in Expanding the geographic and geochronologic range of early pinnipeds: New specimens of Enaliarctos from Northern California and Oregon
Fig. 8. Time calibrated composite phylogenetic hypothesis of early pinnipedimorphs and putative allies, with an emphasis on Oligo-Miocene pinnipedimorphs from the eastern North Pacific. Topology based on Boessenecker and Churchill (2015), except as follows: Enaliarctos from Berta (1991); Phocoidea after Boessenecker and Churchill (in press). Placement of Pacificotaria from Deméré and Berta (2001), conjectural placement (dashed lines) of Puijila and Kolponomos after Tedford et al. (1994) and Rybczynski et al. (2009), Enaliarctos sp. (UWBM 89114) based on shared dental synapomorphies with E. emlongi and E. mitchelli. Geochronologic ranges from Table 3 (this study), Boessenecker and Churchill (2015: supplementary information, in press: supplementary information), and Rybczynski et al. (2009).
Fig. 4 in Expanding the geographic and geochronologic range of early pinnipeds: New specimens of Enaliarctos from Northern California and Oregon
Fig. 4. Metacarpal of pinniped mammal Enaliarctos mealsi Mitchell and Tedford, 1973 (UCMP 276804) from Schooner Gulch, Mendocino County, California, earliest Miocene; in dorsal (A), lateral (B), and ventral/palmar C) views.
Fig. 2 in Expanding the geographic and geochronologic range of early pinnipeds: New specimens of Enaliarctos from Northern California and Oregon
Fig. 2. Stratigraphic columns of Oregon (A) and California (B) localities. Columns based on Snavely et al. (1964) and Phillips et al. (1976); paleomagnetic and K/Ar dates from Prothero et al. (2001a, b) and Phillips et al. (1976). In the interest of clarity non-enaliarctine marine carnivores are omitted. Modified from Moore (1963) and Phillips et al. (1976). Abbreviations: FAD, first appearance datum; LAD, last appearance datum; t, type locality/horizon.
Fig. 2. A in Prevalence and geographic distribution of Babesia conradae and detection of Babesia vogeli in free-ranging California coyotes (Canis latrans)
Fig. 2. A) PCR positivity (indicated by color) of coyotes (Canis latrans) carcasses recovered (▴) in each county between 2015 and 2019. B) Map of southern California including Los Angeles, Orange, Ventura, San Bernardino, Riverside, and San Diego counties showing B. conradae PCR positivity (indicated by color) in each city where coyote carcasses were recovered. The number of coyotes sampled at each location is indicated by the size of the circle.
Fig. 3 in Prevalence and geographic distribution of Babesia conradae and detection of Babesia vogeli in free-ranging California coyotes (Canis latrans)
Fig. 3. Maximum likelihood phylogenetic tree of Babesia positive coyotes (Canis latrans) collected in California from 2015 to 2019 with 7 different published reference sequences from other Babesia species for comparison. Scale bar represents percent of genetic variation along tree branches. Labels include coyote ID and location found. Alphanumeric values in parenthesis denote published GenBank sequence. Clades in <60% of bootstraps are collapsed.
Fig. 1 in Prevalence and geographic distribution of Babesia conradae and detection of Babesia vogeli in free-ranging California coyotes (Canis latrans)
Fig. 1. Base pair differences in a 70 base pair region of the 18S gene from Babesia conradae DNA sequences isolated from California coyotes (Canis latrans) splenic samples collected between 2015 and 2019 compared to published sequence available in GenBank.
Fig. 3 in A tale of two nematodes: Climate mediates mustelid infection by nematodes across the geographical range
Fig. 3. Prediction of prevalence and infection intensity of Aonchotheca putorii and Molineus patens in the Northern Hemisphere based on averaged model estimates, using the WorldClim climate data set. Areas outside of the range of climatic variables used for model fitting are filled with checkerboard pattern. Transparency of the prediction colour reflects the coefficient of variation (CV) of predicted values (i.e. more uncertain prediction has more pattern tint). Predictions assumed the stomach was included in the analyses. (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 A tale of two nematodes: Climate mediates mustelid infection by nematodes across the geographical range
Fig. 1. Geographical location of study sites for the nematode parasites Aonchotheca putorii and Molineus patens, within the Palaearctic and Nearctic in seven mustelid host species. Details of the samples are given in Table S1.
Fig. 2 in A tale of two nematodes: Climate mediates mustelid infection by nematodes across the geographical range
Fig. 2. Model results for Aonchotheca putorii and Molineus patens infection parameters in seven mustelid species. Panels show model-averaged predictions of prevalence and infection intensity depending on the part of the alimentary tract analysed and climatic conditions (seasonality in precipitation and mean temperature of the warmest quarter). Points and lines show the mean, whiskers or shading denote 95% confidence intervals. Remaining explanatory variables were kept at their mean values or most common factor levels. The distribution of the data is shown at the bottom axes as a histogram or density plots.
Figure 3 in New adult host records for three Buprestidae (Coleoptera) rarely encountered in the United States and significant extension of the known geographic range of Agrilus pilosicollis Fisher
Figure 3. Dicerca mutica LeConte, ♂. a) Dorsal view. b) Ventral view. c) Lateral view. d) 5th abdomi-
Figure 2 in New adult host records for three Buprestidae (Coleoptera) rarely encountered in the United States and significant extension of the known geographic range of Agrilus pilosicollis Fisher
Figure 2. Agrilus pilosicollis Fisher ♀. a) Dorsal view. b) Ventral view. c) Lateral view. d) Lateral view of pronotum. e) Proclaw.
Figure 6 in Courtship song of the South African lacewing Chrysoperla zastrowi (Esben-Petersen) (Neuroptera: Chrysopidae): evidence for a trans-equatorial geographic range?
Figure 6. Scatterplot of the first two roots of a discriminant function analysis of nine song features (see text) of Cc5, C. zastrowi, C. lucasina, C. mediterranea and C. agilis. Each data point represents a single individual, coded by taxon.
Figure 2 in Courtship song of the South African lacewing Chrysoperla zastrowi (Esben-Petersen) (Neuroptera: Chrysopidae): evidence for a trans-equatorial geographic range?
Figure 2. Oscillograms (volts on y-axis) and sonagrams (Hertz on y-axis) of typical solo (non-dueting) vibrational songs. (A) Cc5, five volleys or shortest repeated units (SRUs); (B) Cc5, detail of a single volley/SRU; (C) C. zastrowi, five volleys or shortest repeated units (SRUs), drawn to same time scale as A. Song features discussed in the text are labeled.
Figure 4 in Courtship song of the South African lacewing Chrysoperla zastrowi (Esben-Petersen) (Neuroptera: Chrysopidae): evidence for a trans-equatorial geographic range?
Figure 4. Two key morphological features of lacewing taxa. (A) Fore wing of Cc5 (above) and C. zastrowi (beneath). Note the contrasting perpendicular versus oblique orientation of the Rs-M crossvein in the two taxa. (B) Lateral view of the lip/chin of sternite 8+9 of the male abdominal apex. Letters A–G represent landmarks used to determine relative shapes and sizes of the lip and chin. All specimens of both Cc5 and C. zastrowi showed line segment AB.BC, indicating a relatively broad, protruding lip.
Figure 3 in Courtship song of the South African lacewing Chrysoperla zastrowi (Esben-Petersen) (Neuroptera: Chrysopidae): evidence for a trans-equatorial geographic range?
Figure 3. Oscillograms comparing typical heterosexual duets, drawn to the same time scale. (A) Cc5; (B) C. zastrowi. Note the presence of occasional transient volley breaks (arrows) in the songs of both taxa.
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.