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Fig. 21 in Palaeoecology of tropical marine invertebrate assemblages from the Late Triassic of Misurina, Dolomites, Italy
Fig. 21. Heterobranch gastropods from Misurina Landslide, northern Italy, Cassian Formation, Carnian, Upper Triassic. A. Promathildia cf. decorata Klipstein, 1843), PZO 12729, in lateral (A1) and apical (A3) views; A2, close up to show heterostrophic protoconch, in lateral view. B. Promathildia subnodosa (Münster, 1841), PZO 12730, in apertural view. C. Promathildia cf. milierensis Zardini, 1980; PZO 12722, in apertural view (C1); C2, close up to show heterostrophic protoconch, in lateral view; C3, close up to show heterostrophic protoconch, transition to teleoconch well visible, in lateral view. D. Promathildia cf. milierensis Zardini, 1980, PZO 12725, in lateral view. E. Promathildia cf. milierensis Zardini, 1980, PZO 12723, in lateral view. F. Promathildia cf. milierensis Zardini, 1980, PZO 12726, in lateral view. G. Camponaxis lateplicata (Klipstein, 1843), PZO 12731, in lateral view. H. Promathildia cf. milierensis Zardini, 1980, PZO 12727, in lateral view. I. Promathildia cf. milierensis Zardini, 1980; PZO 12724, in lateral view.
Fig. 5 in Bone histology of the graviportal dinocephalian therapsid Jonkeria from the middle Permian Tapinocephalus Assemblage Zone of the Karoo Basin of South Africa
Fig. 5. Transverse section of the rib (BP/1/5409) of cf. Jonkeria sp. from the middle Permian Tapinocephalus Assemblage Zone of the Karoo Basin of South Africa. A1, overall view of the rib showing the highly cancellous nature of the cortex; note that only the top area of the section preserves the compact cortical bone tissue. A2, A3, detail showing slight change in the tissue type around the lines of arrested growths but overall matrix is woven; note: numbers associated with arrowheads indicate lines of arrested growth (LAGs) in ascending order from the medullary region to periosteal periphery. A4, detail showing enlarged erosional cavities (inset). A5, detail showing fibrolamellar bone between lines of arrested growth. A6, detail showing dense woven matrix; note the change in the density of osteocyte lacunae around the LAG (number associated with arrowhead indicates LAG). Abbreviation: wb, woven bone. Photographs under ordinary light (A1, A3, A4, A5), and cross-polarized light with lambda compensator (A2, A6).
Fig. 2 in Bone histology of the graviportal dinocephalian therapsid Jonkeria from the middle Permian Tapinocephalus Assemblage Zone of the Karoo Basin of South Africa
Fig. 2. Transverse sections of the radius (SAM-PK-12233b) of Jonkeria parva (Boonstra, 1955) from the middle Permian Tapinocephalus Assemblage Zone of the Karoo Basin of South Africa. A1, diaphyseal cross-section showing highly vascularized fibrolamellar bone tissue in the outer cortex and the medullary cavity filled with bony trabeculae; note: the numerous enlarged resorption cavities in the perimedullary region. A2, detail showing an annulus with lamellar bone (arrowhead). A3, detail showing extension of an annulus in the cortex (arrowhead). B1, fibrolamellar bone tissue with woven matrix in the outer cortex showing circumferential and reticular organization of the vascular canals; B2, B3, detail showing the change to a reticular organization of the vascular canals. Abbreviations: mr, medullary region; po, primary osteon; tb, trabeculae; wb, woven bone. Photographs under cross-polarized light with lambda compensator (A1–A3, B1, B2) and ordinary light (B3).
Fig. 4 in Bone histology of the graviportal dinocephalian therapsid Jonkeria from the middle Permian Tapinocephalus Assemblage Zone of the Karoo Basin of South Africa
Fig. 4. Thin section of a core of the humerus (SAM-PK-11994) of Jonkeria ingens (Broom, 1923) from the middle Permian Tapinocephalus Assemblage Zone of the Karoo Basin of South Africa. A1, overall view of humerus showing laminar fibrolamellar bone in the outer cortex and the increasingly cancellous nature of the bone towards the medullary cavity; note: numerous enlarged resorption cavities in the perimedullary cavity, and the layer of indurated sediments at the top of the section. A2, A3, highly vascularized laminar fibrolamellar bone. A4, A5, details showing a few isolated simple longitudinal vascular canals and primary osteons. A6, A7, detail showing large resorption cavities lined by narrow deposit of lamellar bone (arrows). Abbreviations: po, primary osteons; rc, resorption cavity; wb, woven bone. Photographs under ordinary light (A1, A2, A4, A6), and cross-polarized light with lambda compensator (A3, A5, A7).
Fig. 3 in Bone histology of the graviportal dinocephalian therapsid Jonkeria from the middle Permian Tapinocephalus Assemblage Zone of the Karoo Basin of South Africa
Fig. 3. Transverse sections of the tarsal (SAM-PK-12233c) of Jonkeria parva (Boonstra, 1955) from the middle Permian Tapinocephalus Assemblage Zone of the Karoo Basin of South Africa. A1, diaphyseal cross-section showing highly vascularized fibrolamellar bone tissue in the outer cortex and cancellous bone tissue with extensively developed bony trabeculae in the medullary cavity; note: numerous enlarged resorption cavities in the perimedullary region. A2, detail showing highly vascularized reticular FLB. A3, A4, detail showing simple longitudinal vascular canals. A5, A6, detail showing reticular vascular canals. Photographs under cross-polarized light with lambda compensator (A1–A3, A5) and ordinary light (A4, A6).
Fig. 6 in Bone histology of the graviportal dinocephalian therapsid Jonkeria from the middle Permian Tapinocephalus Assemblage Zone of the Karoo Basin of South Africa
Fig. 6. Longitudinal section of the rib (BP/1/5409) of cf. Jonkeria sp. from the middle Permian Tapinocephalus Assemblage Zone of the Karoo Basin of South Africa. A1, overall view of the rib showing highly secondarily remodeled cortex; note: numerous enlarged resorption cavities. A2, detail showing woven bone and enlarged resorption spaces. Photographs under ordinary light (A1) and cross-polarized light with lambda compensator (A2).
Fig. 8 in Oligocene plant assemblage from Rębiszów, Lower Silesia: First "volcanic flora" from Poland
Fig. 8. Angiosperms impressions from Łysa Góra near Rębiszów, Poland, late Oligocene. A. Dombeyopsis lobata Unger, 1850, KRAM-P 128/462, leaf. B. cf. Rosa lignitum Heer, 1869, KRAM-P 128/401, leaf. Scale bars 5 mm.
Fig. 6 in Oligocene plant assemblage from Rębiszów, Lower Silesia: First "volcanic flora" from Poland
Fig. 6. Angiosperms impressions from Łysa Góra near Rębiszów, Poland, late Oligocene. A. cf. Trigonobalanopsis rhamnoides (Rossmässler, 1849) Walther and Kvaček, 1988, KRAM-P 128/305, leaf. B. Trigonobalanopsis exacantha (Mai, 1970) Kvaček and Walther, 1988, KRAM-P 128/185, cupules. C. Quercus sp. or Castanopsis sp., KRAM-P 128/313, fruit. D. Populus cf. zaddachii Heer, 1959, KRAM-P 128/511, leaf. E. Sloanea artocarpites (Ettingshausen, 1869) Kvaček and Hably, 2001, KRAM-P 128/433, leaf. F, G. cf. "Quercus" bavarica Knobloch and Kvaček, 2004, leaves. F. KRAM-P 128/79. G. KRAM-P 128/212. H. Eotrigonobalanus furcinervis (Rossmässler, 1840) Walther and Kvaček, 1989, KRAM-P 128/234, leaf. Scale bars: A–C, 5 mm; D–H, 10 mm.
Fig. 5 in Oligocene plant assemblage from Rębiszów, Lower Silesia: First "volcanic flora" from Poland
Fig. 5. Angiosperms impressions from Łysa Góra near Rębiszów, Poland, late Oligocene. A. Carpinus sp. vel Ostrya sp., KRAM-P 128/546, leaf. B. Paliurus favonii Unger, 1847, KRAM-P 128/165, fruit. C, D, F. Majanthemophyllum basinerve (Rossmässler, 1840) Knobloch and Kvaček, 1996, leaves. C. KRAM-P 128/571. D. KRAM-P 128/289. F. KRAM-P 128/212. E. Vitis sp. or Ampelopsis sp., KRAM-P 128/205, leaf. G. Ampelopsis cf. rotundata Chandler, 1925, KRAM-P 128/109, seed. Scale bars: A, C–F, 10 mm; B, G, 1 mm.
Fig. 3 in Oligocene plant assemblage from Rębiszów, Lower Silesia: First "volcanic flora" from Poland
Fig. 3. Angiosperms impressions from Łysa Góra near Rębiszów, Poland, late Oligocene. A. Alnus julianiformis (Sternberg, 1823) Kvaček and Holy, 1974, KRAM-P 128/347, leaf. B. Ulmus fischeri Heer, 1856, KRAM-P 128/149, leaf. C. Liriodendron haueri Ettingshausen, 1869, KRAM-P 128/318, fruit. D. Acer cf. hercynicum Mai, 1978, KRAM-P 128/118, fruit. E. Craigia bronnii (Unger, 1845) Kvaček, Bůžek, and Manchester, 1991, KRAM-P 128/203, fruit. F. Alnus kefersteinii (Goeppert, 1838) Unger, 1845, KRAM-P 128/44, infructescence. Scale bars: A, B, F, 10 mm; C, D, 5 mm; E, 2 mm.
Fig. 7 in Oligocene plant assemblage from Rębiszów, Lower Silesia: First "volcanic flora" from Poland
Fig. 7. Angiosperms impressions from Łysa Góra near Rębiszów, Poland, late Oligocene. A, E. cf. Cedrela macrophylla Andreánszky, 1955, leaves. A. KRAM-P 128/570. E. KRAM-P 128/516. B. Alnus cf. gaudinii (Heer, 1856) Knobloch and Kvaček, 1976, KRAM-P 128/390, leaf. C. cf. Acer tricuspidatum Bronn, 1838, KRAM-P 128/388, leaf. D. Prunus cf. scharfii Gregor, 1978, KRAM-P 128/352, endocarp. Scale bars: A–C, E, 10 mm; D, 1 mm.
Fig. 4 in Oligocene plant assemblage from Rębiszów, Lower Silesia: First "volcanic flora" from Poland
Fig. 4. Angiosperms impressions from Łysa Góra near Rębiszów, Poland, late Oligocene. A. cf. Laurophyllum acutimontanum Mai, 1963, leaf, KRAM-P 128/436. B–D. Daphnogene cinnamomifolia (Brongniart, 1822) Unger, 1850 forma lanceolata sensu Kvaček and Walther (1995), leaves. B. KRAM-P 128/131. C. KRAM-P 128/397. D. KRAM-P 128/298. E. Daphnogene cinnamomifolia (Brongniart, 1822) Unger, 1850 forma cinnamomifolia sensu Kvaček and Walther (1995), KRAM-P 128/256, leaf. F. Acer cf. polymorphoides Mai, 1987, KRAM-P 128/415, fruit. G. Mahonia sp., KRAM-P 128/35, leaf. H. Tsuga cf. moenana Kirchheimer, 1935, KRAM-P 128/75, cone. I. Ostrya atlantidis Unger, 1850, KRAM-P 128/318, fruit. J. cf. Leguminosites sp. or cf. Rhodomyrtophyllum sp., KRAM-P 128/88, leaf. K. Mahonia sp., KRAM-P 128/291, leaf. Scale bars: A–E, 10 mm; H, G, 5 mm; K, 3 mm; F, H, J, 2.5 mm; I, 1 mm.
Fig. 2 in Oligocene plant assemblage from Rębiszów, Lower Silesia: First "volcanic flora" from Poland
Fig. 2. Conifers impressions from Łysa Góra near Rębiszów, Poland, late Oligocene. A. Calocedrus suleticensis (Brabenec, 1909) Kvaček, 1999, KRAM-P 128/38, twig. B. cf. Tsuga sp., KRAM-P 128/50, twigs. C. Cunninghamia cf. miocenica Ettingshausen, 1872, KRAM-P 128/251, cone scale. D. Cryptomeria cf. rhenana Kilpper, 1968, KRAM-P 128/1; twigs (D1), cone (D2). Scale bars: A, B, D1, 10 mm; C, D2, 5 mm.
Fig. 5 in Multispecies leatherback turtle assemblage from the Oligocene Chandler Bridge and Ashley formations of South Carolina, USA
Fig. 5. Ossicles of leatherback turtle cf. Psephophorus sp. from Oligocene of South Carolina, USA. CCNHM 5460 (A) and CCNHM 5543 (B), in dorsal A1, B1), visceral (A2, B2), and sutural (A3, B3) views.
Fig. 3 in Multispecies leatherback turtle assemblage from the Oligocene Chandler Bridge and Ashley formations of South Carolina, USA
Fig. 3. Ossicles of leatherback turtle Natemys sp. 2 from Oligocene of South Carolina, USA. CCNHM 4287.1 (A), CCNHM 4287.2 (B), and CCNHM 4910 (C), in dorsal (A1–C1), visceral (A2–C2), and sutural (A3–C3) views. Arrows indicate the fissure on the visceral and sutural surfaces of CCNHM 4287.2, and note the stratified internal structure of CCNHM 4287.1.
Figure 2 in Polychaete assemblages associated with the invasive green alga Avrainvillea amadelpha and surrounding bare sediment patches in Hawaii
Figure 2. nMDS ordinations of polychaete assemblages: A, using data of all taxa; B, bubbles indicating abundance in number of individuals; C, bubbles indicating values of Shannon–Wiener diversity; D, bubbles indicating values of Pielou's Evenness.
Figure 1 in Polychaete assemblages associated with the invasive green alga Avrainvillea amadelpha and surrounding bare sediment patches in Hawaii
Figure 1. Map of the study area showing the algae ('A' stations; circles) and sediment stations ('S' stations; squares).
Figure 1 in Shallow-water polychaete assemblages in the northwestern Mediterranean Sea and its possible use in the evaluation of good environmental state
Figure 1. (Upper left graph) Map of the studied zone. Blue circles represent sampled stations from the Gulf of Lions and red circles from the Northern Mediterranean Spanish coast. (Lower graph) Schematic diagram showing the distribution of the four studied communities in the mesoscale studied area
Fig. 3 - A in Decapod assemblage from the late Miocene (early-middle Messinian) of the Romagna Apennines nearby Brisighella, Emilia-Romagna (N Italy)
Fig. 3 - A) Monodaeus bortolottii Delle Cave, 1988, MSF 2300 (x 2.6). B) Goneplax cf. G. gulderi Bachmayer, 1953, MSF 2332 (x 10). C) Family, genus and species indet., MSF 2316 (x 16.6).
Fig. 2 - A in Decapod assemblage from the late Miocene (early-middle Messinian) of the Romagna Apennines nearby Brisighella, Emilia-Romagna (N Italy)
Fig. 2 - A) Galathea cf. G. weinfurteri Bachmayer, 1950, MSF 2337 (x 3.1). B) Medorippe ampla Garassino, De Angeli, Gallo Pasini, 2004, MSF 2317 (x 8). C) Palaeomyra bispinosa A. Milne Edwards in E. Sismonda, 1861, MSF 2314 (x 3).
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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.