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Fig. 3 in New remains attributable to the holotype of the sauropod dinosaur Neuquensaurus australis, with implications for saltasaurine systematics
Fig. 3. Holotypic sacrum of the sauropod Neuquensaurus australis (Lydekker, 1893), MLP Ly 7, from the Late Cretaceous of Neuquén, Argentina. Close−up stereophotographs of sutures between sacral vertebrae 3–6 in ventral view.
Fig. 6 in New remains attributable to the holotype of the sauropod dinosaur Neuquensaurus australis, with implications for saltasaurine systematics
Fig. 6. Holotypic caudal vertebrae of the sauropod Neuquensaurus australis (Lydekker, 1893) from the Late Cretaceous of Neuquén, Argentina. A. MLP Ly 2,?second or third caudal vertebra in left lateral (A1), anterior (A2), posterior (A3), and ventral (A4) views. B. MLP Ly 3,?seventh caudal vertebra in left lateral (B1), anterior (B2), posterior (B3), and ventral (B4) views. C. MLP Ly 5a, b, parts of the?ninth and tenth caudal vertebrae in left lateral (C1), anterior (C2), posterior (C3), and ventral (C4) views. D. MLP Ly 4, mid−caudal vertebra in left lateral (D1), anterior (D2), posterior (D3), and ventral (D4) views. E. MLP Ly 6, mid−posterior caudal vertebra in left lateral (E1), anterior (E2), posterior (E3), and ventral (E4) views. Abbreviation: sprl, spinoprezygapophyseal lamina.
Fig. 3 in An ailuravine rodent from the lower Eocene Cambay Formation at Vastan, western India, and its palaeobiogeographic implications
Fig. 3. Ailuravine rodent Meldimys musak sp. nov., from the lower Eocene Cambay Formation at Vastan (Gujarat, western India), isolated cheek teeth. A. GU/RSR/VAS 608, right dP4, paratype, stereo pair in occlusal view. B. GU/RSR/VAS 606, left P4 (reversed), paratype, stereo pair in occlusal view. C. GU/RSR/VAS 128, left M1 (reversed), paratype in anterior (C1), occlusal (C2 stereo), and posterior (C3) views. D. GU/RSR/VAS 449, right M1, stereo pair in occlusal view. E. GU/RSR/VAS 454, right M2 in occlusal (E1 stereo), posterior (E2), anterior (E3), buccal (E4), and lingual (E5) views; F. GU/RSR/VAS 450, right M2 in occlusal (F1 stereo) and posterior (F2) views. G. GU/RSR/VAS 609, right M2, holotype in buccal (G1), lingual (G2), anterior (G3), occlusal (G4 stereo), and posterior (G5) views.
Ephemeral Piscivory in a Mesopredator Sunfish: Implications for Pond Food Webs
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Figure 7 in Paleohistological studies of bone and teeth in Gyrodus circularis (Gyrodidae: Pycnodontiformes: Actinopterygii). Phylogenetic implications for the Gyrodidae
Figure 7. – Gyrodus circularis. (MNHN. JRE 540). Ground transversal sections (transmitted natural light). A: (MNHN-F-Histos 2748) Detail of alveolar bone showing numerous osteocytes with there ramified osteocytic canalicles. B: (MNHN-F-Histos 2743) Detail of the prearticular bony tissue with some vascular cavities and/or canals (vc). The white arrowheads point to osteoblastic canalicles. C: (MNHNF-Histos 2743) Detail of the contact dentine/bony tissue (de/bo). Bony tissue is crossed by some osteoblastic canalicles whose apical end is ramified (arrowheads). The arrows point to a cementing line between bone and dentine. D: (MNHN-F-Histos 2746) Detail of some osteoblastic canalicles (arrows) starting from vascular canals (vc) in the alveolar bone and of some star-shaped osteocytes (arrowheads). The end of the right osteoblastic canalicle is clearly ramified. Scale bars: A = 25 μm; B = 100 μm; C = 25 μm); D = 25 μm.
Figure 4 in Paleohistological studies of bone and teeth in Gyrodus circularis (Gyrodidae: Pycnodontiformes: Actinopterygii). Phylogenetic implications for the Gyrodidae
Figure 4. – Gyrodus circularis. Ground transversal sections of the teeth roots (transmitted natural light). A: (MNHN-F-Histos 2748) Detail of the orthodentine (od) showing the apical part of the odontoblastic canalicles that are clearly ramified to their extrem- ity (arrows); bo: bone. Inset: detail of a terminal ramification. B: The section (MNHN-F-Histos 2748) shows the contact between the orthodentine (od) with the alveolar bone (bo). The pulp surface of the dentine shows thin mineralized spherules (arrowheads) that project in the pulp cavity; pc = pulp cavity; vc: vascular cavity. C: (MNHN-F-Histos 2743) Detail of the spheritic orthodentine showing the Liesegang lines that mark the successive steps of mineralization in proportion of the thickening of the tooth. The upper Liesegang line is edged by mineralized spherules. The black arrowheads point to the more recent mineralized spherules that project in the pulp cavity (pc). Inset: Detail of several mineralized spherules (white arrowheads) inside the dentinous tissue (arrows). Scale bars: A = 25 μm; Inset A = 10 μm; B = 50 μm; C = 50 μm; inset C = 25 μm.
Figure 3 in Paleohistological studies of bone and teeth in Gyrodus circularis (Gyrodidae: Pycnodontiformes: Actinopterygii). Phylogenetic implications for the Gyrodidae
Figure 3. – Gyrodus circularis. (MNHN. JRE 540). Axial ground section (MNHN-F-Histos 2743). Detail of the crown of teeth No 1. The two parts of the dentine core are clearly seen: the circumpulpar orthodentine (od) with its fine laminations (arrowheads) and the upper thick layer of acrodine (ac) that is crossed by the odontoblastic canalicles that progressively get thinner and stop before the surface of the crown (arrow). The black pigmentation is restricted to the more external acrodine layer. The spheritic dentine (sd) is clearly seen at the top of the pulp cavity (pc). Scale bar = 10 μm.
Figure 2 in Paleohistological studies of bone and teeth in Gyrodus circularis (Gyrodidae: Pycnodontiformes: Actinopterygii). Phylogenetic implications for the Gyrodidae
Figure 2. – Gyrodus circularis. (MNHN. JRE 540). Ground sections (MNHN-F-Histos 2743) (transmitted natural light). A: Axial section (see Fig. 1) of a molariform tooth inserted in a bony sock- et (sb). The dentine walls show numerous mineralized granules (arrowheads). The asterisks point to neighbouring teeth. The alveolar bony tissue runs lightly over the base of the crown. ac: acrodine; bo: bony tissue; oc: odontoblastic canalicles; od: osteodentine. B to D: Three successive transversal sections of five neighbouring teeth (see Fig. 1), crossing different levels of the pulp cavities. Section B (MNHN-F-Histos 2745) crosses the apical crown of the smaller teeth and the higher part of the pulp cavity of the larger tooth. Section C (MNHN-F-Histos 2746) crosses the mid part of the pulp cavities of smaller teeth and the base of pulp cavity of the large one. Section D (MNHN-F-Histos 2748) crosses a relatively low part of the smaller teeth and the base of the pulp cavity of the larger tooth as revealed by the bony arches that occupy the main part of the pulp lumen (arrowhead). The pulp cavities of the four left teeth are circular whereas the pulp cavity of the larger right tooth is lightly ovoid. The walls of the pulp cavities of the five teeth are perfectly circular and constituted of orthodentine. The circum pulpar dentine shows spheritic mineralization (see Figs 3, 4). Each tooth is surrounded by spongy bony tissue characterized by thin trabeculae (see Fig. 6). Scale bars: A = 500 μm; B-D: = 2 mm.
Fig. 2 in Systematics of limbless scincid lizards from northern Madagascar: morphology, phylogenetic relationships and implications for classification (Squamata: Scincidae)
Fig. 2 Paracontias minimus in life. a Dorsolateral view. b Head, lateral view
Fig. 3 in The biology of an isolated Mashona mole-rat population from southern Malawi, with implications for the diversity and biogeography of the genus Fukomys
Fig. 3 Karyogram of a male Fukomys darlingi from Nsanje, Malawi; 2n = 54; aFN = 76. The chromosomes were paired by eye and ordered according to the position of the centromere and chromosome size. The X chromosome was arbitrarily designated. The vertical bar represents 10 µm
Fig. 2 in The biology of an isolated Mashona mole-rat population from southern Malawi, with implications for the diversity and biogeography of the genus Fukomys
Fig. 2 Selected Fukomys molerats from Malawi and adjacent regions. Shown are representatives of F. whytei from southern Tanzania (top left), nominate F. darlingi from Zimbabwe (top right), and F. darlingi from Nsanje in southern Malawi (below left: in the field on the day of capture; below right: captive family at the University of South Bohemia in České Budějovice). Photos by Tim Jackson and R. Šumbera
FIGURE 6 in Morphological convergences in Ameles Burmeister and Pseudoyersinia Kirby: Taxonomic implications of wing reduction and flight predisposition in some West-Mediterranean Amelini (Insecta: Mantodea)
FIGURE 6. Ameles maroccana, male habitus from Moulay-Yakoub (Morocco). Photo by R. Battiston.
FIGURE 2 in Morphological convergences in Ameles Burmeister and Pseudoyersinia Kirby: Taxonomic implications of wing reduction and flight predisposition in some West-Mediterranean Amelini (Insecta: Mantodea)
FIGURE 2. Ameles andreae, male habitus from Sardinia (Italy). Photo by R. Battiston.
Supplementary material 4 from: Davoli F, Cozzo M, Angeli F, Groff C, Randi E (2018) Infanticide in brown bear: a case-study in the Italian Alps – Genetic identification of perpetrator and implications in small populations. Nature Conservation 25: 55-75. https://doi.org/10.3897/natureconservation.25.23776
Table S1. Detailed results of the biological model (consensus and composite) :
Supplementary material 1 from: Davoli F, Cozzo M, Angeli F, Groff C, Randi E (2018) Infanticide in brown bear: a case-study in the Italian Alps – Genetic identification of perpetrator and implications in small populations. Nature Conservation 25: 55-75. https://doi.org/10.3897/natureconservation.25.23776
Text S1. Parameters used for parentage analysis :
Supplementary material 3 from: Davoli F, Cozzo M, Angeli F, Groff C, Randi E (2018) Infanticide in brown bear: a case-study in the Italian Alps – Genetic identification of perpetrator and implications in small populations. Nature Conservation 25: 55-75. https://doi.org/10.3897/natureconservation.25.23776
Text S3. Detailed results of LRmix STUDIO for each suspected male: Global Composite (ADO 0.55) :
Supplementary material 2 from: Davoli F, Cozzo M, Angeli F, Groff C, Randi E (2018) Infanticide in brown bear: a case-study in the Italian Alps – Genetic identification of perpetrator and implications in small populations. Nature Conservation 25: 55-75. https://doi.org/10.3897/natureconservation.25.23776
Text S2. Detailed results of LRmix STUDIO for each suspected male: Global Consensus (ADO 0.65) :
Supplementary material 1 from: Karam-Gemael M, Izzo T, Chagas-Jr A (2018) Why be red listed? Threatened Myriapoda species in Brazil with implications for their conservation. In: Stoev P, Edgecombe GD (Eds) Proceedings of the 17th International Congress of Myriapodology, Krabi, Thailand. ZooKeys 741: 255-269. https://doi.org/10.3897/zookeys.741.21971
Myriapoda threatened species geographic coordinates :
Figure 3 from: Karam-Gemael M, Izzo T, Chagas-Jr A (2018) Why be red listed? Threatened Myriapoda species in Brazil with implications for their conservation. In: Stoev P, Edgecombe GD (Eds) Proceedings of the 17th International Congress of Myriapodology, Krabi, Thailand. ZooKeys 741: 255-269. https://doi.org/10.3897/zookeys.741.21971
Figure 3 Distribution of the Brazilian Myriapoda threatened species. The color of the legend represents the IUCN threatened category: red (Critically endangered – CR), orange (Endangered – EN), and yellow (Vulnerable – VU). Species in blue are only known from subterranean habitats. Species with an asterisk (*) occur inside PAs.
Figure 2 from: Karam-Gemael M, Izzo T, Chagas-Jr A (2018) Why be red listed? Threatened Myriapoda species in Brazil with implications for their conservation. In: Stoev P, Edgecombe GD (Eds) Proceedings of the 17th International Congress of Myriapodology, Krabi, Thailand. ZooKeys 741: 255-269. https://doi.org/10.3897/zookeys.741.21971
Figure 2 Myriapoda species assessement by the current Brazilian Red List. Myriapoda threatened species according to the 2014 Brazilian Red List, which follows IUCN classification categories (CR = Critically endangered, EN = Endangered, VU = Vulnerable, NT = Near threatened, LC = Least concern, DD = Data deficient). Dashed red line indicates threatened categories.
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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.