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Fig. 8 in New bioerosion traces in rhynchosaur bones from the Upper Triassic of Brazil and the oldest occurrence of the ichnogenera Osteocallis and Amphifaoichnus
Fig. 8. Indiscrete borings on bone fragments of the rhynchosaurid archosauromorph Hyperodapedon mariensis (Tupi Caldas, 1933) from Buriol Site, Brazil, Hyperodapedon AZ, Carnian. A. UFRGS-PV-1581-T #3; A1, a boring in the opposite face of the arthropod bioerosion trace fossil Amphifaoichnus, but also penetrating it; A2, close up view showing the presence of bone chips in the base of the boring. B. UFRGS-PV-1581-T #7 showing a boring with one rounded termination. C. UFRGS-PV-1581-T #9; C1, an elongated boring with a rounded termination and bone chips scattered on the base; C2, close up view highlighting the bone chips scattered on the base.
Fig. 1. Geological and geographic context. A in New bioerosion traces in rhynchosaur bones from the Upper Triassic of Brazil and the oldest occurrence of the ichnogenera Osteocallis and Amphifaoichnus
Fig. 1. Geological and geographic context. A. Location of the Paraná Basin in Brazil. B. Limits of the Triassic rocks of Rosário do Sul Group and the Triassic rocks of Paraná Basin in Rio Grande do Sul state. C. Location of the Buriol Site, locality of UFRGS-PV-1581-T, and nearby Predebon and Janner sites. D. Chrono-, lito-, and biostratigraphy of southern Brazilian Triassic (modified from Schultz et al. 2020). Arrow indicates stratigraphical position of UFRGS-PV-1581-T; * refers to absolute ages from Langer et al. (2018); ** refers to absolute ages from Philipp et al. (2018).
Fig. 7 in New bioerosion traces in rhynchosaur bones from the Upper Triassic of Brazil and the oldest occurrence of the ichnogenera Osteocallis and Amphifaoichnus
Fig. 7. Subcircular clusters on bone fragments of the rhynchosaurid archosauromorph Hyperodapedon mariensis (Tupi Caldas, 1933) from Buriol Site, Brazil, Hyperodapedon AZ, Carnian. A. UFRGS-PV-1581-T #17; A1, subcircular cluster connected to a cluster of grooves; A2, schematic drawing. B. UFRGS-PV-1581-T #13; B1, subcircular cluster associated to an irregular cluster of grooves (arrow), possibly a partially preserved subcircular cluster; B2, schematic drawing. C. UFRGS-PV-1581-T #16 showing an isolated subcircular cluster of grooves.
Fig. 3 in New bioerosion traces in rhynchosaur bones from the Upper Triassic of Brazil and the oldest occurrence of the ichnogenera Osteocallis and Amphifaoichnus
Fig. 3. Arthropod bioerosion trace fossil Amphifaoichnus isp. on bone fragments of the rhynchosaurid archosauromorph Hyperodapedon mariensis (Tupi Caldas, 1933) from Buriol Site, Brazil, Hyperodapedon AZ, Carnian. A. UFRGS-PV-1581-T #3; A1, close up showing Amphifaoichnus isp. (note the bone chips) associated to a perpendicular boring (dashed outline) and feeding traces of Osteocallis mandibulus Roberts et al., 2007 (arrow; see also Fig. 4A1); A2, axial view of µCT scan showing the internal morphology of the tube, meniscate structures and the perpendicular boring; A3, coronal view of µCT scan showing the trace (dotted surface) and the destruction of both cortical (black outline) and trabecular bone. B. UFRGS-PV-1581-T #4; B1, specimen arrow) showing the uneven distribution of bone chips in the filling; B2, specimen in transversal view showing the rounded morphology of the filling. C. UFRGS-PV-1581-T #10; C1, specimen in negative relief with a small portion of filling still preserved (arrow); C2, close up of filling; C3, specimen in transversal view showing the U-shape of the boring.
Fig. 4 in Ephemeral Occurrence of the Echiuran Listriolobus brevirostris (Annelida: Echiura) in Osaka Bay between 1995 and 2002; a New Record for Japan, Probably Resulting from Human-mediated Introduction
Fig. 4. Relationship between trunk length and proboscis length in 52 fixed specimens of Listriolobus brevirostris, collected from Osaka Bay in 1999 (NSMT-Ec 164 to 183).
Fig. 3 in Ephemeral Occurrence of the Echiuran Listriolobus brevirostris (Annelida: Echiura) in Osaka Bay between 1995 and 2002; a New Record for Japan, Probably Resulting from Human-mediated Introduction
Fig. 3. Internal morphology (dorsal view) of Listriolobus brevirostris from Osaka Bay, collected off Kobe on 26 November 2001 (NSMT-Ec 186). A, anterior end of trunk; B, posterior end of trunk (ventral vessel undetectable due to deterioration). Abbreviations: al, alimentary canal; av, anal vesicle; dv, dorsal vessel; gd, gonoduct; gl, gonostomal lip; im, interbasal muscle; nv, neurointestinal vessel; rc, rectal caecum; re, rectum; rv, ring vessel; tb, terminal bulb; vn, ventral nerve cord: vs, ventral seta; vv, ventral vessel. Scale bars: 1 mm.
Fig. 5 in Ephemeral Occurrence of the Echiuran Listriolobus brevirostris (Annelida: Echiura) in Osaka Bay between 1995 and 2002; a New Record for Japan, Probably Resulting from Human-mediated Introduction
Fig. 5. Seasonal changes in trunk length of Listriolobus brevirostris from Osaka Bay in 1999. Solid bars indicate mature specimen(s), dotted lines, measurements from live specimens, and double-headed arrow of dotted line, the length range in live specimens (see text).
FIG. 1 in New occurrences of crabs (Decapoda, Brachyura, Eubrachyura) in the Pliocene of Florida (United States)
FIG. 1. — Location map of the two fossiliferous localities of the Pliocene Tamiami Formation in Sarasota County, Florida (United States). Locality A: SMR Aggregates quarry (27°20'05"N, 82°19'58"W). Locality B: Old APAC Shell quarry (27°14'18"N, 82°27'11"W). Maps modified after different sources and ViaMichelin.
FIG. 2 in New occurrences of crabs (Decapoda, Brachyura, Eubrachyura) in the Pliocene of Florida (United States)
FIG. 2. — Persephona cf. P. subovata (Rathbun, 1893), USNM PAL 720104 from the Pinecrest Member of Tamiami Formation (middle Piacenzian, Pliocene) of locality A in Sarasota County, Florida (United States): A, dorsal view; B, frontal view; C, left lateral view; D, posterior view. Scale bar: 10 mm. Photographs by À. Ossó.
FIG. 3 in New occurrences of crabs (Decapoda, Brachyura, Eubrachyura) in the Pliocene of Florida (United States)
FIG. 3. — Paractaea cf. P. nodosa (Stimpson, 1860), USNM PAL 720105 from the Pinecrest Member of Tamiami Formation (middle Piacenzian, Pliocene) of locality B in Sarasota County, Florida (United States): A, dorsal view; B, frontal view; C, posterior view. Scale bar: 10 mm. Photographs by À. Ossó.
Figure 1 in A new species of Amblydromalus Chant & McMurtry (Acari: Phytoseiidae), with notes on occurrence of genus in South America
Figure 1 Amblydromalus amazonicusn. sp., female: A – Dorsal idiosoma; B – Ventral idiosoma; C – Spermatheca; D – Chelicera; E – Genu, tíbia and basitarsus of leg IV. Male: F – Ventrianal shield; G – Spermatodactyl.
Figures 128–129 in Scorpions of the Horn of Africa (Arachnida: Scorpiones). Part XXX. Parabuthus (Buthidae) (Part III), with description of three new species from Somaliland and occurrence of Parabuthus eritreaensis Kovařík, 2003
Figures 128–129: Figure 128. Map showing confirmed distribution of Parabuthus spp. In Djibouti, Eritrea, Ethiopia, Somalia, and Somaliland. Figure 129. Parabuthus eritreaensis, female from Somaliland in vivo habitus.
Figures 103–110 in Scorpions of the Horn of Africa (Arachnida: Scorpiones). Part XXX. Parabuthus (Buthidae) (Part III), with description of three new species from Somaliland and occurrence of Parabuthus eritreaensis Kovařík, 2003
Figures 103–110: Parabuthus quincyae sp. n., male holotype. Figure 103. Carapace and tergites I–IV. Figures 104–105. Sternopectinal area and sternites. Figure 106. Sternite VII and metasoma I–II ventral Figures 107–110. Right legs I–IV, retrolateral aspect.
Figures 72–93 in Scorpions of the Horn of Africa (Arachnida: Scorpiones). Part XXX. Parabuthus (Buthidae) (Part III), with description of three new species from Somaliland and occurrence of Parabuthus eritreaensis Kovařík, 2003
Figures 72–93: Figures 72–82: Parabuthus evae sp. n., male holotype. Figures 83–93: Parabuthus cimrmani, male holotype. Figures 72–93. Right pedipalp, chela in dorsal (72, 83), external (73, 84), and ventral (74, 85) views, patella in dorsal (75, 86), external (76, 87), and ventral (77, 88) views, femur and trochanter in internal (78, 89), dorsal (79, 90), and ventral (80, 91) views. Dentate margins of movable (81, 92) and fixed (82, 93) fingers. Trichobothrial pattern indicated in Figures 73–76 and 78–79 by white circles.
Figures 62–71 in Scorpions of the Horn of Africa (Arachnida: Scorpiones). Part XXX. Parabuthus (Buthidae) (Part III), with description of three new species from Somaliland and occurrence of Parabuthus eritreaensis Kovařík, 2003
Figures 62–71: Parabuthus evae sp. n., male holotype. Figure 62. Carapace and tergites I–V. Figure 63. Sternopectinal area and sternites. Figures 64–67. Right legs I–IV, retrolateral aspect. Figure 68. Metasoma V, and telson in lateral view. Figures 69–71. Metasoma and telson in lateral (69), ventral (70), and dorsal (71) views. Scale bars: 10 mm (69–71).
Figures 98–102 in Scorpions of the Horn of Africa (Arachnida: Scorpiones). Part XXX. Parabuthus (Buthidae) (Part III), with description of three new species from Somaliland and occurrence of Parabuthus eritreaensis Kovařík, 2003
Figures 98–102: Parabuthus quincyae sp. n., male holotype. Figure 98. Metasoma V, and telson in lateral view. Figure 99. Metasoma I–III in dorsal view.Figures 100–102. Metasoma and telson in lateral (100), ventral (101), and dorsal (102) views. Scale bar: 10 mm (100–102).
Figures 60–61 in Scorpions of the Horn of Africa (Arachnida: Scorpiones). Part XXX. Parabuthus (Buthidae) (Part III), with description of three new species from Somaliland and occurrence of Parabuthus eritreaensis Kovařík, 2003
Figures 60–61. Parabuthus evae sp. n., male holotype, in dorsal (60) and ventral (61) views. Scale bar: 10 mm.
Figures 49–53 in Scorpions of the Horn of Africa (Arachnida: Scorpiones). Part XXX. Parabuthus (Buthidae) (Part III), with description of three new species from Somaliland and occurrence of Parabuthus eritreaensis Kovařík, 2003
Figures 49–53: Parabuthus dorisae sp. n., male holotype.. Figures 49–52. Right legs I–IV, retrolateral aspect. Figure 53. Type locality, Somaliland, vicinity of God Heeli.
Figures 58–59 in Scorpions of the Horn of Africa (Arachnida: Scorpiones). Part XXX. Parabuthus (Buthidae) (Part III), with description of three new species from Somaliland and occurrence of Parabuthus eritreaensis Kovařík, 2003
Figures 58–59: Parabuthus evae sp. n., male holotype. Figure 58. Female holotype in vivo habitus. Figure 59. Locality, Somaliland, E of Las Anod.
Figures 29–35 in Scorpions of the Horn of Africa (Arachnida: Scorpiones). Part XXX. Parabuthus (Buthidae) (Part III), with description of three new species from Somaliland and occurrence of Parabuthus eritreaensis Kovařík, 2003
Figures 29–35: Parabuthus dorisae sp. n. Figure 29. Juvenile paratype 60 mm long, metasoma IV–V and telson lateral. Figure 30. Juvenile paratype 27 mm long, metasoma and telson lateral. Figures 31–35: Male holotype. Figure 31. Metasoma V, and telson in lateral view. Figure 32. Metasoma I–III in dorsal view.Figures 33–35. Metasoma and telson in lateral (33), ventral (34), and dorsal (35) views. Scale bars: 10 mm (29–30, 33–35).
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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.