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Figure 8 in Two new species of Bonnetina tarantulas (Theraphosidae: Theraphosinae) from Mexico: contributions to morphological nomenclature and molecular characterization of types
Figure 8. Bonnetina tenuiverpis sp. n. (A) Type locality (near Zuluapan, State of Mexico, Mexico); (B) landscape surrounding type locality. Photos by Carlos E. Santibáñez.
Figure 13 in Two new species of Bonnetina tarantulas (Theraphosidae: Theraphosinae) from Mexico: contributions to morphological nomenclature and molecular characterization of types
Figure 13. Bonnetina juxtantricola sp. n. Female allotype. (A) Carapace; (B) posterior margin of carapace, showing thick erect setae; (C) ocular area, dorsal view; (D) sternum; (E) labium and maxillae; (F) spermatheca, dorsal view; (G) spermatheca, ventral view. Scale lines: 1 mm.
Figure 5 in Two new species of Bonnetina tarantulas (Theraphosidae: Theraphosinae) from Mexico: contributions to morphological nomenclature and molecular characterization of types
Figure 5. Bonnetina tenuiverpis sp. n. Male holotype. (A) Left tibia–metatarsus I joint, ventral view, showing prolateral (left) and retrolateral (right) apophyses; (B) left tibia–metatarsus I joint, retrolateral view, showing retrolateral (left) and accessory (front) apophyses and nodule of granules; (C) left metatarsus I, prolateral view. Arrow indicates nodule of granules. Scale lines: 0.5 mm.
Figure 4 in Two new species of Bonnetina tarantulas (Theraphosidae: Theraphosinae) from Mexico: contributions to morphological nomenclature and molecular characterization of types
Figure 4. Bonnetina tenuiverpis sp. n. Male holotype, left pedipalpal bulb, SEM images. (A) Embolus apical half, prolateral view; (B) embolus apex, ventral–frontal view; (C) apex, prolateral view; (D) apex, frontal view. Arrow colours represent keels: prolateral superior (black), sperm pore (white), dorsal (grey) and prolateral inferior (hatched). Chevron: sperm pore. Scale lines: 10 µm (except A: 100 µm).
Figure 12 in Two new species of Bonnetina tarantulas (Theraphosidae: Theraphosinae) from Mexico: contributions to morphological nomenclature and molecular characterization of types
Figure 12. Bonnetina juxtantricola sp. n. Male holotype. (A) Left tibia–metatarsus I joint, ventral view, showing prolateral (left) and retrolateral (right) apophyses; (B) left tibia–metatarsus I joint, retrolateral view, showing retrolateral (left) and accessory (front) apophyses and nodule of granules; (C) left metatarsus I, prolateral view. White arrows: nodule of granules; grey arrows: basal metatarsi I rounded structures. Scale lines: 1 mm.
Figure 11 in Two new species of Bonnetina tarantulas (Theraphosidae: Theraphosinae) from Mexico: contributions to morphological nomenclature and molecular characterization of types
Figure 11. Bonnetina juxtantricola sp. n. Male holotype, right pedipalpal bulb, SEM images. (A) Embolus, prolateral view; (B) sperm pore; (C) embolus, ventral–retrolateral view; (D) apex, frontal view. Arrow colours represent keels: prolateral superior (black), sperm pore (white), prolateral sub-apical (grey) and prolateral inferior (hatched). Chevron: sperm pore.
Figure 7 in Two new species of Bonnetina tarantulas (Theraphosidae: Theraphosinae) from Mexico: contributions to morphological nomenclature and molecular characterization of types
Figure 7. Bonnetina tenuiverpis sp. n. Spermathecae. (A) Female allotype, dorsal view; (B) female allotype, ventral view; (C) female paratype AMNH, dorsal view; (D) female paratype CNAN-T0757, dorsal view. Scale lines: 1 mm.
Figure 6 in Two new species of Bonnetina tarantulas (Theraphosidae: Theraphosinae) from Mexico: contributions to morphological nomenclature and molecular characterization of types
Figure 6. Bonnetina tenuiverpis sp. n. Female allotype. (A) Carapace; (B) posterior margin of carapace, showing thin setae; (C) ocular area, dorsal view; (D) sternum; (E) labium and maxillae; (F) ventral view of metatarsus and tarsus of left leg III. Scale lines: 1 mm.
Figure 1 in Two new species of Bonnetina tarantulas (Theraphosidae: Theraphosinae) from Mexico: contributions to morphological nomenclature and molecular characterization of types
Figure 1. Bonnetina tenuiverpis sp. n. Habitus. (A) Male holotype; (B) female allotype. Scale line: 10 mm. Photos by David Ortiz.
Figure 1 from: Salvador RB, Ablett JD (2020) Type specimens of Streptaxidae from Henry C. Burnup in the collection of the Museum of New Zealand Te Papa Tongarewa. African Invertebrates 61(2): 107-117. https://doi.org/10.3897/afrinvertebr.61.58085
Figure 1 Burnup's type specimens in the NMNZ collection. All figures to scale (bar = 1 mm), except for Fig. 1G, not to scale (bar = 0.5 mm) A paratype of Ennea farquhari var. avena Burnup, 1914, NMZN M.207153 B paratype of Ennea farquhari var. avena Burnup, 1914, NMZN M.207154 C paratype of Ennea maritzburgensis var. contracta Burnup, 1914, NMNZ M.207175 D paratype of Ennea darglensis var. illovoensis Burnup, 1914, NMNZ M.207156 E paratype of Ennea inhluzaniensis Burnup, 1914, NMNZ M.207160 F specimen of Gulella elliptica manca (Burnup, 1914), NMNZ M.207151 G paratype of Ennea melvilli Burnup, 1914, NMNZ M.207157 H paratype of Ennea mooiensis Burnup, 1914, NMNZ M.207158 I paratype of Ennea ponsonbyi Burnup, 1914, NMNZ M.207159 J paratype of Ennea isipingoensis var. sturanyi Burnup, 1914, NMNZ M.207149.
Data from: A new method for estimating locomotion type in large ground birds
Estimating the locomotion type of fossil ground birds is necessary for a better understanding of their ecology. Until now, only one method has allowed us to estimate the locomotion of fossil ground birds, but its application is complicated in the majority of fossil cases because it requires data from the three bones from the same hindlimb of one individual. Here, we propose a new method using only the maximum length and minimum width of the tarsometatarsus to estimate the locomotion of these fossil birds. This method is easy to apply and better distinguishes the intermediate cases between graviportal (walking) and cursorial (running) birds. This study shows that the species of large ground birds of the families Gastornithidae and Brontornithidae were all graviportal, probably because of their large body mass. More unexpectedly, it also shows that some Phorusrhacidae (e.g. Paraphysornis), usually described as cursorial birds, were in fact graviportal, probably because of their considerable body mass. All these new data about locomotion provide a better understanding of the ecology of fossil ground birds.
FIGURE 2 in Status of Cyrtosia marginata Perris (Diptera: Mythicomyiidae) with remarks on the type and new distribution records
FIGURE 2. Cyrtosia marginata Perris, male habitus, lateral view. From Jersey, Channel Islands.
FIGURE 20. Erenna cornuta Pugh, 2001. Type B bracts. Scale bar 5 in A description of two new species of the genus Erenna (Siphonophora: Physonectae: Erennidae), with notes on recently collected specimens of other Erenna species
FIGURE 20. Erenna cornuta Pugh, 2001. Type B bracts. Scale bar 5 mm.
FIGURE 19. Erenna cornuta Pugh, 2001. Type A bracts. Scale bar 5 in A description of two new species of the genus Erenna (Siphonophora: Physonectae: Erennidae), with notes on recently collected specimens of other Erenna species
FIGURE 19. Erenna cornuta Pugh, 2001. Type A bracts. Scale bar 5 mm.
FIGURE 8 in A new species of Tanacetipathes from Brazil, with a redescription of the type species T. tanacetum (Pourtales) (Cnidaria, Anthozoa, Antipatharia)
FIGURE 8. Holotype of Tanacetipathes paula, n. sp (MNRJ 6031). Spines on pinnules.
FIGURE 18 in Two new species of Pamphobeteus Pocock 1901 (Araneae: Mygalomorphae: Theraphosidae) from Brazil, with a new type of stridulatory organ
FIGURE 18. Pamphobeteus grandis sp. nov.. Male. Photo: Rick C. West.
FIGURES 7–8 in Two new species of Pamphobeteus Pocock 1901 (Araneae: Mygalomorphae: Theraphosidae) from Brazil, with a new type of stridulatory organ
FIGURES 7–8. Pamphobeteus crassifemur sp. nov.. 7, Male. 8, Female. Photos: R. Bertani.
FIGURE 2 in Long-legged flies (Diptera: Dolichopodidae) in the collection of the Natal Museum: A review of C. H. Curran's types, new synonyms, and new combinations
FIGURE 2. Acropsilus vorax (Curran), hypopygium, left lateral view. Scale bar: 0.1 mm
FIGURE 1 in Long-legged flies (Diptera: Dolichopodidae) in the collection of the Natal Museum: A review of C. H. Curran's types, new synonyms, and new combinations
FIGURE 1. Acropsilus vorax (Curran), wing. Scale bar: 0.5 mm.
FIGURE 1 in Two new species of Chondrocladia (Demospongiae: Cladorhizidae) with a new spicule type from the deep south Pacific, and a discussion of the genus Meliiderma
FIGURE 1. Maps showing the collecting areas.
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.