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Fig. 2 in The youngest ctenocystoids from the Upper Ordovician of the United Kingdom and the evolution of the bilateral body plan in echinoderms
Fig. 2. Stratigraphical position (A) and geographical location (B) of the site where Conollia sporranoides sp. nov. was collected. Adapted from Ingham (1992).
Fig. 3 in The youngest ctenocystoids from the Upper Ordovician of the United Kingdom and the evolution of the bilateral body plan in echinoderms
Fig. 3. Ctenocystoid echinoderm Conollia sporranoides sp. nov. from the Upper Ordovician of Scotland, UK. A. GLAHM 131255/1, partial specimen. B. GLAHM 131255/2, complete specimen. C. GLAHM 131255/3, partial ctenidium in lateral view. D. GLAHM 131255/4, partial ctenidium in adoral view. E. GLAHM 131255/5, partial ctenidium. F. GLAHM 131255/6, partial ctenidium. G. GLAHM 131255/7, complete ctenidium in anterior view. H. GLAHM 131255/8, partial ctenidium in anterior view. I. GLAHM 131255/9, partial ctenidium in anterior view. Photographs of original specimens (A, B), latex casts whitened with ammonium chloride sublimate (C–F), and virtual reconstructions (G–I). Abbreviations: as, articulations for serrated spines; cp, ctenoid plates; ss, serrated spines; ts, thecal spines.
Fig. 1. Representative Cambrian ctenocystoid echinoderms. A, B in The youngest ctenocystoids from the Upper Ordovician of the United Kingdom and the evolution of the bilateral body plan in echinoderms
Fig. 1. Representative Cambrian ctenocystoid echinoderms. A, B. Ctenocystis utahensis Robison and Sprinkle, 1969 from Cambrian Series 3 of the United States. USNM 163252 in dorsal (A 1) and anterior (A 2) views; USNM 595079 in right lateral view (B). C. Undescribed ctenocystoid (Ctenocystoid gen. et sp. nov 1 in Smith et al. 2013) from Cambrian Series 3 of Morocco. NHMUK EE 15428 in dorsal view. D. Courtessolea moncereti Domínguez Alonso, 2004 from Cambrian Series 3 of France. MNHN F.A45783 in dorsal view. E. Courtessolea sp. from Cambrian Series 3 of Spain. MPZ 2009/1234b in ventral view. F. Undescribed ctenocystoid (Ctenocystoid gen. et sp. nov 2 in Smith et al. 2013) from Cambrian Series 3 of Morocco. NHMUK EE 15317 in ventral view. G, H. Jugoszovia archaeocyathoides Dzik and Orłowski, 1995 from Cambrian Series 3 of Poland. ZPAL Ec1/9 in ventral view (G); ZPAL Ec1/1 in anterior view (H). All specimens are latex casts whitened with ammonium chloride sublimate.
Fig. 1 in Trypanosoma cruzi infection in mammals in Florida: New insight into the transmission of T. cruzi in the southeastern United States
Fig. 1. Sampling scheme for the multiscale spatial analysis depicting the sampled sites in Florida. In the state-wide map, green circles indicate a sampled area within the estimated distribution of Triatoma sanguisuga in Florida (gray shaded region) and red circles indicate a sampled site outside of this distribution. The inset depicts the paired site design (peridomestic = blue, sylvatic = green, nearest township to the sampled area = red diamonds, and the average distance of capture from the nearest inhabited household = site associated meter distance). The map was created using QGIS Geographic Information System version 3.22.5-Białowie˙za, htt p://qgis.osgeo.org. County layers map (TIGER/Line Shapefile, 2016, state, Florida, Current County Subdivision State-based) and city locations (TIGER/Line Shapefile, Current, State, Florida, Places) was accessed from the United States Census Bureau, https://catalog.data.gov/dataset. (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 Detection of Dirofilaria immitis via integrated serological and molecular analyses in coyotes from Texas, United States
Fig. 1. Texas locations where samples were collected, including Webb, Maverick, Jim Hogg, Haskell, Throckmorton, Hutchinson, Roberts, Reeves, and Loving counties.
Fig. 2. Maximum likelihood tree constructed from partial cox1 in Spirometra infection in a captive Samar cobra (Naja samarensis) in the United States: An imported case?
Fig. 2. Maximum likelihood tree constructed from partial cox1 gene sequences of Spirometra samples and related taxa. HKY + G + I was used as the best substitution model. Schistocephalus solidus and Dibothriocephalus nihonkaiensis were used as outgroups. (JPN – Japan; KOR – South Korea; CHI and CHN – China; AUS – Australia; IRA – Iran; USA – United States; THA – Thailand; MMR – Myanmar; TZA – Tanzania; IND – India; VNM – Vietnam; KHM – Cambodia; LAO – Laos; COL – Colombia; NZL – New Zealand; IDN – Indonesia; ROU – Romania; SSD – South Sudan; ETH – Ethiopia; POL – Poland; UKR – Ukraine; FIN – Finland; CHL – Chile; BRA – Brazil).
Fig. 1. A in Spirometra infection in a captive Samar cobra (Naja samarensis) in the United States: An imported case?
Fig. 1. A) Presence of Spirometra plerocercoid in subcutaneous tissue of a male Samar cobra (Naja samarensis) from a zoological facility in the USA; B) Plerocercoids isolated from de subcutaneous tissue of the same specimen.
Fig. 1 in Dirofilaria immitis and Dirofilaria striata (Spirurida: Onchocercidae) detected in wild carnivores from Texas, United States
Fig. 1. Map of Texas, US indicating the origin and number of animals sampled by species. Counties of Texas from which samples originated are in blue. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)
Fig. 2. Phylogenetic tree created using a in Dirofilaria immitis and Dirofilaria striata (Spirurida: Onchocercidae) detected in wild carnivores from Texas, United States
Fig. 2. Phylogenetic tree created using a maximum likelihood method (2000 bootstrap replicates) showing the relationship of identified Dirofilaria immitis and one isolate of Dirofilaria striata. Brugia pahangi sequence was used as outgroup.
FIGURE 7 in Two new species of Pseudaetobatus Cappetta, 1986 (Batoidei: Myliobatidae) from the southeastern United States
FIGURE 7. Myliobatiform ray teeth associated with Pseudaetobatus in Alabama and South Carolina, comparative specimens of Aetobatus irregularis from Alabama, and late Eocene Rhinoptera sp. from Georgia. 1, Rhinoptera sp. (Tallahatta Formation), MSC 33915, incomplete median tooth, labial (1.1), lingual (1.2), and occlusal (1.3) views. 2, Rhinoptera sp. (Dry Branch Formation), SC 2001.1.12, lateral tooth, labial (2.1), lingual (2.2), and occlusal (2.3) views. 3, Rhinoptera sp. (Clinchfield Formation), SC 2013.44.8, lateral tooth, labial (3.1), lingual (3.2), and occlusal (3.3) views. 4, Aetomylaeus sp. (Tallahatta Formation), MSC 33931, incomplete lower median tooth, labial (4.1), lingual (4.2), and occlusal (4.3) views. 5, Aetomylaeus sp. (Dry Branch Formation), SC 2001.1, incomplete lower median tooth, labial (5.1), lingual (5.2), and occlusal (5.3) views. 6, Rhinoptera sp. (Clinchfield Formation), SC 2013.44.9, distal-most lateral tooth similar to Pseudaetobatus sp., labial (6.1), lingual (6.2), and occlusal (6.3) views. 7-8, Aetobatus irregularis (Lisbon Formation). 7, SC 2012.47.24, incomplete lower median tooth, occlusal view. 8, SC 2012.47.26, left side of upper? median tooth, distal (8.1), labial (8.2), and occlusal (8.3) views. Scale bars equal 1.0 cm.
FIGURE 5 in Two new species of Pseudaetobatus Cappetta, 1986 (Batoidei: Myliobatidae) from the southeastern United States
FIGURE 5. Pseudaetobatus belli sp. nov. from lower Eocene strata of Alabama and Mississippi. 1, MSC 12699.1, partial upper median tooth, baso-labial (1.1), lingual oblique (1.2), occlusal (1.3), and profile (1.4) views. 2, MSC 35078, partial lower median tooth, labial (2.1), lingual (2.2), lingual oblique (2.3), occlusal (2.4), and profile (2.5) views. 3, MSC 35055, lower right distal-most lateral tooth, basal (3.1), distal (3.2), labial (3.3), mesial (3.4), and occlusal (3.5) views. 4, MSC 35081, partial median tooth, basal (4.1), labial (4.2), lingual (4.3), lingual oblique (4.4), and profile (4.5) views. 5, MSC 35049, lower median tooth, occlusal view. 6, MSC 35071, partial lower median tooth, lingual oblique (6.1), and profile (6.2) views. 7, MSC 35050, lower median tooth, occlusal view. 8, MSC 35061, upper right distal-most lateral tooth, occlusal (8.1), and basal (8.2) views. 9, MSC 12776, upper right distal-most lateral tooth, basal (9.1), labial (9.2), lingual oblique (9.3), occlusal (9.4), distal (9.5), and mesial (9.6) views. 10, MSC 35080, partial median tooth, lingual (10.1), lingual oblique (10.2), and occlusal (10.3) views. 11, MSC 35056, lower right distal-most lateral tooth, distal (11.1), labial (11.2), lingual (11.3), mesial (11.4), and occlusal (labial at left) (11.5) views. 12, MSC 35060, upper right distal-most lateral tooth, basal (12.1), labial (12.2), lingual oblique (12.3), occlusal (12.4), mesial (12.5), and distal (12.6) views. 13, MSC 35079, partial lower median tooth, lingual oblique (13.1), and occlusal (13.2) views. 14, MSC 35065, nearly complete lower median tooth, occlusal view. 15, MSC 35052, partial lower median tooth, occlusal view. Scale bars equal 1.0 cm.
FIGURE 4 in Two new species of Pseudaetobatus Cappetta, 1986 (Batoidei: Myliobatidae) from the southeastern United States
FIGURE 4. Pseudaetobatus belli sp. nov. hypodigm from the type stratum within the lower Eocene (NP 13) Tallahatta Formation, Dale County, Alabama. 1, MSC 35048, lower median tooth, oblique lingual (1.1), occlusal (1.2), basal (1.3), labial (1.4), and lingual (1.5) views. 2, MSC 35054, lower right distal-most lateral tooth, occlusal (2.1), basal (2.2), distal (2.3), mesial (2.4), and labial (2.5) views. 3, MSC 35059, upper right distal-most lateral tooth, oblique lingual (3.1), occlusal (3.2), basal (3.3), and labial (3.4) views. 4, MSC 35062, intermediate lateral tooth, occlusal (4.1) (labial at top), lingual (4.2), labial (4.3), mesial (4.4), and distal (4.5) views. 5, MSC 35058, partial upper? median tooth, occlusal view. 6, Occlusal view of hypothetical reconstruction of part of the lower dentition. This consists of specimens shown in 1 (MSC 35048), 2 (MSC 35054), 4 (MSC 35062), and Figure 5.3 (MSC 35055). 2, 4, and Figure 5.3 were reduced in size to be consistent with 1. 4 was replicated and reversed to represent the left and right tooth rows. 2 and Figure 5.3 are from the right side but were reversed to represent the left side. The resulting composite series was then replicated. Scale bars equal 1.0 cm.
FIGURE 3 in Two new species of Pseudaetobatus Cappetta, 1986 (Batoidei: Myliobatidae) from the southeastern United States
FIGURE 3. Chronostratigraphy, lithostratigraphy, and biostratigraphy of middle-to-upper Eocene strata of south-central South Carolina. Abbreviation: O'burg = Orangeburg.
FIGURE 2 in Two new species of Pseudaetobatus Cappetta, 1986 (Batoidei: Myliobatidae) from the southeastern United States
FIGURE 2. Chronostratigraphy, lithostratigraphy, and biostratigraphy of lower-to-middle Eocene strata of eastern Mississippi and Alabama. Modified from Bybell and Gibson (1985).
FIGURE 1 in Two new species of Pseudaetobatus Cappetta, 1986 (Batoidei: Myliobatidae) from the southeastern United States
FIGURE 1. Generalized geographic map of the southeastern United States, with counties from which Pseudaetobatus teeth were recovered (highlighted in light gray). Specific localities indicated by black dots. 1, Whynot locality, Lauderdale County, MS; 2, site AWa-1, Washington County, AL; 3, site ABu-3, Butler County, AL; 4, site ADl-1, Dale County (type locality Pseudaetobatus belli), AL; 5, Dry Branch localities, Aiken County, SC.
FIGURE 6 in Two new species of Pseudaetobatus Cappetta, 1986 (Batoidei: Myliobatidae) from the southeastern United States
FIGURE 6. Pseudaetobatus undulatus sp. nov. hypodigm and other specimens from the upper Eocene Dry Branch Formation, Aiken County, South Carolina. 1, SC 2013.38.91, upper right distal-most lateral tooth (holotype), basal (1.1), distal (1.2), labial (1.3), mesial (1.4), lingual oblique (1.5), and occlusal (1.6) views. 2, SC 2001.1.4.1, upper left distal-most lateral tooth, labial (2.1), lingual (2.2), and occlusal (2.3) views. 3, SC 2013.38.93.3, lower left distal-most lateral tooth, labial (3.1), lingual (3.2), and occlusal (3.3) views. 4, SC 2001.1.5.2, intermediate lateral tooth (paratype), basal (4.1), distal (4.2), labial (4.3), mesial (4.4), lingual oblique (4.5), and occlusal (4.6) views. 5, SC 2001.1.5.1 (paratype), lower right distal-most lateral tooth, mesial (5.1), lingual oblique (5.2), distal (5.3), labial (5.4), and occlusal (5.5) views. 6, SC 2013.38.84, lower median tooth (paratype), lingual oblique (6.1), basal (6.2), and occlusal (6.3) views. 7, SC 2013.38.90, lower median tooth, lingual oblique view. 8, SC 2013.38.86, upper median tooth (paratype), lingual oblique (8.1), baso-lingual (8.2), and occlusal (8.3) views. 9, Occlusal view of hypothetical reconstruction of part of the upper dentition. This consists of specimens shown in 1 (SC 2001.1.5.2), and 8 (SC 2013.38.86. 1 and 4 were reduced in size to be consistent with 8, and they were reversed to also represent the right tooth rows. The resulting composite series was then replicated. 10, SC 2013.38.85, upper median tooth, occlusal view. Scale bars equal 0.5 cm.
FIGURE 4 in Amateur paleontological societies and fossil clubs, interactions with professional paleontologists, and social paleontology in the United States
FIGURE 4. (Top) Percentage of total responses (N=40) about content and information preferences for future activities that might be mediated by FOSSIL. (Bottom) Examples of real-world (practical) skills for future activities.
FIGURE 3 in Amateur paleontological societies and fossil clubs, interactions with professional paleontologists, and social paleontology in the United States
FIGURE 3. Perceived comfort (%) of amateur respondents contacting other amateurs versus professionals. Along the x-axis, 1 represents "Not comfortable," whereas 6 is "Comfortable," and 7 is "Very Comfortable."
FIGURE 9 in Amateur paleontological societies and fossil clubs, interactions with professional paleontologists, and social paleontology in the United States
FIGURE 9. Theoretical model of the end-members and spectrum of motivations for participating in paleontology.
FIGURE 7 in Amateur paleontological societies and fossil clubs, interactions with professional paleontologists, and social paleontology in the United States
FIGURE 7. Comparison of the growth in the following modes of communication for the FOSSIL project: Facebook likes, Twitter followers, e-newsletter subscribers, Listserv subscribers, and FOSSIL project website, www.myfossil.org.
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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)
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.