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Text-fig. 6. Ornithorhynchus anatinus. Transverse section through the otic region of the head of a 180-mm specimen. ls: supracapsular lamina; lsc: lateral semicircular canal; mt: musculus temporalis; opa: parietal bone; opl: pluteal bone; ppe: parietal process of endocranium (blue). (Modified from Zeller 1989.) in Cartilago Teniformis And Its Derivatives: Additional Information On The Basic Composition And Evolution Of The Skull
Text-fig. 6. Ornithorhynchus anatinus. Transverse section through the otic region of the head of a 180-mm specimen. ls: supracapsular lamina; lsc: lateral semicircular canal; mt: musculus temporalis; opa: parietal bone; opl: pluteal bone; ppe: parietal process of endocranium (blue). (Modified from Zeller 1989.)
Text-fig. 5. Dorsal view of endocranium of 93 mm human fetus. Derivatives of the teniform cartilages blue. con: orbitonasal commissure; lp: parietal lamina; oc: orbital cartilage; rco: remnants of orbitoparietal commissure. (Modified from Reinbach 1963; cf. Bersch and Reinbach 1970.) in Cartilago Teniformis And Its Derivatives: Additional Information On The Basic Composition And Evolution Of The Skull
Text-fig. 5. Dorsal view of endocranium of 93 mm human fetus. Derivatives of the teniform cartilages blue. con: orbitonasal commissure; lp: parietal lamina; oc: orbital cartilage; rco: remnants of orbitoparietal commissure. (Modified from Reinbach 1963; cf. Bersch and Reinbach 1970.)
Text-fig. 2. Soft-tissue imprints and traces of bioerosion on Middle Ordovician cephalopods from Estonia. a: GIT 819-1, Tragoceras falcatum (SCHLOTHEIM, 1820), drag bands; b: GIT 819-1, T. falcatum, pseudosutures; c: GIT 819-2, Estonioceras sp., drag bands; d: GIT 819-3, cf. Anthoceras vaginatum (SCHLOTHEIM, 1820), drag bands; e: GIT 819-4, cf. Orthoceras regulare SCHLOTHEIM, 1820, drag bands; f: Pits on the body chamber of GIT 819-1, T. falcatum. Specimens oriented with aperture downwards. Scale bars 1 mm. in Conch Structures, Soft-Tissue Imprints And Taphonomy Of The Middle Ordovician Cephalopod Tragoceras Falcatum From Estonia
Text-fig. 2. Soft-tissue imprints and traces of bioerosion on Middle Ordovician cephalopods from Estonia. a: GIT 819-1, Tragoceras falcatum (SCHLOTHEIM, 1820), drag bands; b: GIT 819-1, T. falcatum, pseudosutures; c: GIT 819-2, Estonioceras sp., drag bands; d: GIT 819-3, cf. Anthoceras vaginatum (SCHLOTHEIM, 1820), drag bands; e: GIT 819-4, cf. Orthoceras regulare SCHLOTHEIM, 1820, drag bands; f: Pits on the body chamber of GIT 819-1, T. falcatum. Specimens oriented with aperture downwards. Scale bars 1 mm.
Text-fig. 2. Dorsal view of endocranium of a 31 mm sand lizard (Lacerta agilis). Derivatives of the teniform cartilages blue. cp: cartilago parietectalis (cartilago tecti nasi); cs: sphenethmoidal commissure; tm: taenia marginalis. (Modified from Gaupp 1900.) in Cartilago Teniformis And Its Derivatives: Additional Information On The Basic Composition And Evolution Of The Skull
Text-fig. 2. Dorsal view of endocranium of a 31 mm sand lizard (Lacerta agilis). Derivatives of the teniform cartilages blue. cp: cartilago parietectalis (cartilago tecti nasi); cs: sphenethmoidal commissure; tm: taenia marginalis. (Modified from Gaupp 1900.)
Text-fig. 1. Megastriae and post mortem epicoles on Tragoceras falcatum (SCHLOTHEIM, 1820). Arrows and M1–M3 indicate megastriae, bryozoan colonies are indicated by B1 and B2. a: GIT 819-1, left lateral view; b: body chamber of GIT 819-1, dorsal view; c: body chamber of GIT 819-1, left lateral view; d: GIT 819-1, right lateral view; e: PIMUZ 37299, right lateral view; f: detail of the body chamber of GIT 819-1, right lateral view, encrusted by bryozoans; g: bryozoan colony with Trypanites borings growing on an older bryozoan crust GIT 819-1. Specimens oriented with aperture downwards. Scale bars 10 mm. in Conch Structures, Soft-Tissue Imprints And Taphonomy Of The Middle Ordovician Cephalopod Tragoceras Falcatum From Estonia
Text-fig. 1. Megastriae and post mortem epicoles on Tragoceras falcatum (SCHLOTHEIM, 1820). Arrows and M1–M3 indicate megastriae, bryozoan colonies are indicated by B1 and B2. a: GIT 819-1, left lateral view; b: body chamber of GIT 819-1, dorsal view; c: body chamber of GIT 819-1, left lateral view; d: GIT 819-1, right lateral view; e: PIMUZ 37299, right lateral view; f: detail of the body chamber of GIT 819-1, right lateral view, encrusted by bryozoans; g: bryozoan colony with Trypanites borings growing on an older bryozoan crust GIT 819-1. Specimens oriented with aperture downwards. Scale bars 10 mm.
Text-fig. 2. a–g. Schloenbachia lymensis SPATH, 1926. a–d. S. lymensis from the Plaňany quarry. a. Lateral view. b. Ventral view. c. Whorl section (improved from Soukup 1971). d. Suture line (adopted from Soukup 1971; improved). E – external lobe, A – adventive lobe, U1 and U2 – umbilical lobes. e–g. S. lymensis from the locality Slaný. e, g. Ventro-lateral view showing larger clavi modified into spines closely to the aperture. f. Ventral view. Scale bars equal 10 mm. in Taxonomy And Stratigraphic Distribution Of The Ammonite Schloenbachia Neumayr, 1875 From The Bohemian Cretaceous Basin
Text-fig. 2. a–g. Schloenbachia lymensis SPATH, 1926. a–d. S. lymensis from the Plaňany quarry. a. Lateral view. b. Ventral view. c. Whorl section (improved from Soukup 1971). d. Suture line (adopted from Soukup 1971; improved). E – external lobe, A – adventive lobe, U1 and U2 – umbilical lobes. e–g. S. lymensis from the locality Slaný. e, g. Ventro-lateral view showing larger clavi modified into spines closely to the aperture. f. Ventral view. Scale bars equal 10 mm.
Text-fig. 3. Scanning electron micrographs (a, b) and synchrotron radiation X-ray tomographic microscopy orthoslices (c–e) of flower of Lambertiflora elegans gen. et sp. nov. from the Early Cretaceous Puddledock locality, Virginia, USA (holotype, PP53796, Puddledock sample 082). a) Flower in lateral view showing long pedicel and overlapping elongated tepals; b) Detail of flower showing overlapping elongated tepals; note the numerous holes indicating the position of probable secretory cells; c) Flower in longitudinal section showing overlapping elongated tepals, remains of probable poorly developed stamens or staminodes and probable poorly developed carpels on the central conical gynoecial region of the receptacle (cut between orthoslices xz0510 and 0570); d) Flower in longitudinal section (comparable to c) showing overlapping tepals, poorly developed stamens or staminodes, and probable poorly developed carpels on the central conical gynoecial region of the receptacle; note the prominent cavities from secretory cells scattered through the tissues (cut between orthoslice xz0560 and 0575); e) Flower in transverse section showing overlapping tepals, poorly developed stamens or staminodes, and remains of probable poorly developed carpels (cut between orthoslices xy1160 and 1180). Scale bars = 1 mm (a), 500 µm (b–e). in Multiparted, Apocarpous Flowers From The Early Cretaceous Of Eastern North America And Portugal
Text-fig. 3. Scanning electron micrographs (a, b) and synchrotron radiation X-ray tomographic microscopy orthoslices (c–e) of flower of Lambertiflora elegans gen. et sp. nov. from the Early Cretaceous Puddledock locality, Virginia, USA (holotype, PP53796, Puddledock sample 082). a) Flower in lateral view showing long pedicel and overlapping elongated tepals; b) Detail of flower showing overlapping elongated tepals; note the numerous holes indicating the position of probable secretory cells; c) Flower in longitudinal section showing overlapping elongated tepals, remains of probable poorly developed stamens or staminodes and probable poorly developed carpels on the central conical gynoecial region of the receptacle (cut between orthoslices xz0510 and 0570); d) Flower in longitudinal section (comparable to c) showing overlapping tepals, poorly developed stamens or staminodes, and probable poorly developed carpels on the central conical gynoecial region of the receptacle; note the prominent cavities from secretory cells scattered through the tissues (cut between orthoslice xz0560 and 0575); e) Flower in transverse section showing overlapping tepals, poorly developed stamens or staminodes, and remains of probable poorly developed carpels (cut between orthoslices xy1160 and 1180). Scale bars = 1 mm (a), 500 µm (b–e).
Text-fig. 2. Synchrotron radiation X-ray tomographic microscopy volume renderings (a, b) and orthoslices (c–e) of Mugideiriflora portugallica gen. et sp. nov. from the Early Cretaceous Catefica locality, Portugal (holotype, S174254, Catefica sample 150). Yellow dots – stamens, red dots – carpels. a) Flower in lateral view showing the broad bases of the laminar tepals; b) Flower in longitudinal section showing the flat to slightly concave floral receptacle with a central conical gynoecial region (cut between orthoslices yz0800 and 1220); c) Flower in transverse section showing the numerous laminar tepals in several series and the stamens cut in the region of the poorly differentiated anthers; note cellular differences between outer (op) and inner (in) perianth parts, as well as and transverse sections of anthers, apparently with laterally to slightly dorsally placed pollen sacs (arrow heads) (cut at orthoslice xy0770); d) Flower in transverse section showing the numerous laminar tepals in several series, flattened rhomboidal stamen bases in several series, and poorly differentiated carpels (cut at orthoslice xy0820); e) Flower in transverse section showing the numerous laminar tepals in several series, flattened rhomboidal stamen bases in several series, and poorly differentiated carpels (cut at orthoslice xy0920); f) Flower in longitudinal section showing the shallowly concave floral receptacle with laminar tepals, stamens, and a central conical gynoecial region bearing poorly differentiated carpels (cut at orthoslice yz0900); g) Flower in longitudinal section perpendicular to that in (f) showing stamens and poorly differentiated carpels (cut at orthoslice xz1630). Scale bars = 1 mm (a, b), 500 µm (c–g). in Multiparted, Apocarpous Flowers From The Early Cretaceous Of Eastern North America And Portugal
Text-fig. 2. Synchrotron radiation X-ray tomographic microscopy volume renderings (a, b) and orthoslices (c–e) of Mugideiriflora portugallica gen. et sp. nov. from the Early Cretaceous Catefica locality, Portugal (holotype, S174254, Catefica sample 150). Yellow dots – stamens, red dots – carpels. a) Flower in lateral view showing the broad bases of the laminar tepals; b) Flower in longitudinal section showing the flat to slightly concave floral receptacle with a central conical gynoecial region (cut between orthoslices yz0800 and 1220); c) Flower in transverse section showing the numerous laminar tepals in several series and the stamens cut in the region of the poorly differentiated anthers; note cellular differences between outer (op) and inner (in) perianth parts, as well as and transverse sections of anthers, apparently with laterally to slightly dorsally placed pollen sacs (arrow heads) (cut at orthoslice xy0770); d) Flower in transverse section showing the numerous laminar tepals in several series, flattened rhomboidal stamen bases in several series, and poorly differentiated carpels (cut at orthoslice xy0820); e) Flower in transverse section showing the numerous laminar tepals in several series, flattened rhomboidal stamen bases in several series, and poorly differentiated carpels (cut at orthoslice xy0920); f) Flower in longitudinal section showing the shallowly concave floral receptacle with laminar tepals, stamens, and a central conical gynoecial region bearing poorly differentiated carpels (cut at orthoslice yz0900); g) Flower in longitudinal section perpendicular to that in (f) showing stamens and poorly differentiated carpels (cut at orthoslice xz1630). Scale bars = 1 mm (a, b), 500 µm (c–g).
Text-fig. 1. Scanning electron micrographs of Mugideiriflora portugallica gen. et sp. nov. from the Early Cretaceous Catefica locality, Portugal (holotype, S174254, Catefica sample 150). a) Flower in oblique lateral view showing numerous broad tepals, numerous inwardly curved stamens and the flat floral receptacle with a conical gynoecial region; b–c) Flower in two different oblique apical views showing numerous broad laminar tepals and inwardly curved stamens surrounding the carpels; note cellular differences between outer (op) and inner (in) perianth parts, as well as bases of anthers, apparently with laterally to slightly dorsally placed pollen sacs (arrow heads); d) Detail of flower showing a cluster of poorly differentiated carpels in the center surrounded by elongated stamens; note grooves in the dorsal surface of the stamens indicating the position of the pollen sacs; e) Detail of flower showing the broad bases of the laminar tepals, rhomboidal stamen bases and poorly differentiated carpels; f) Detail of flower showing inwardly arched stamens and poorly differentiated carpels. Scale bars = 1 mm (a–c), 200 µm (d–f). in Multiparted, Apocarpous Flowers From The Early Cretaceous Of Eastern North America And Portugal
Text-fig. 1. Scanning electron micrographs of Mugideiriflora portugallica gen. et sp. nov. from the Early Cretaceous Catefica locality, Portugal (holotype, S174254, Catefica sample 150). a) Flower in oblique lateral view showing numerous broad tepals, numerous inwardly curved stamens and the flat floral receptacle with a conical gynoecial region; b–c) Flower in two different oblique apical views showing numerous broad laminar tepals and inwardly curved stamens surrounding the carpels; note cellular differences between outer (op) and inner (in) perianth parts, as well as bases of anthers, apparently with laterally to slightly dorsally placed pollen sacs (arrow heads); d) Detail of flower showing a cluster of poorly differentiated carpels in the center surrounded by elongated stamens; note grooves in the dorsal surface of the stamens indicating the position of the pollen sacs; e) Detail of flower showing the broad bases of the laminar tepals, rhomboidal stamen bases and poorly differentiated carpels; f) Detail of flower showing inwardly arched stamens and poorly differentiated carpels. Scale bars = 1 mm (a–c), 200 µm (d–f).
Text-fig. 6. Scanning electron micrographs of multicarpellate and apocarpous floral structures from the Early Cretaceous Puddledock locality, Virginia, USA (a, b: PP43701, Puddledock sample 001; c: PP43000x, Puddledock sample 073). a) Anacostia? sp., strongly compressed, elongated receptacle with spirally arranged carpels (red dots; not all shown); note larger size compared to the other floral structures; b) Numerous Anacostia type pollen grains in proximal view from the base of floral structure in (a); note graded reticulum over the proximal pole of the pollen grains; c) Elongated receptacle with numerous carpels in a spiral arrangement, possibly representing an earlier developmental stage of Anacostia? sp. Scale bars = 1 mm (a, c), 10 µm (b). in Multiparted, Apocarpous Flowers From The Early Cretaceous Of Eastern North America And Portugal
Text-fig. 6. Scanning electron micrographs of multicarpellate and apocarpous floral structures from the Early Cretaceous Puddledock locality, Virginia, USA (a, b: PP43701, Puddledock sample 001; c: PP43000x, Puddledock sample 073). a) Anacostia? sp., strongly compressed, elongated receptacle with spirally arranged carpels (red dots; not all shown); note larger size compared to the other floral structures; b) Numerous Anacostia type pollen grains in proximal view from the base of floral structure in (a); note graded reticulum over the proximal pole of the pollen grains; c) Elongated receptacle with numerous carpels in a spiral arrangement, possibly representing an earlier developmental stage of Anacostia? sp. Scale bars = 1 mm (a, c), 10 µm (b).
Text-fig. 3. Tumidopteris astra sp. nov., holotype GIN 4851/343h, morphology of sori. a: part of fertile pinnule; b: one practically complete sorus located on the terminal part of a lateral vein; c: sorus with four visible sporangia; d: partly damaged sorus with three visible sporangia; e: two neighbouring sori. Locality: the borehole IK-675, depth 961.7 m. Scale 1 mm (a, b, e), 500 Μm (c), 100 Μm (d). in A New Species Of The Genus Tumidopteris Naugolnykh From The Permian Of The Pechora Cis-Urals, Russia
Text-fig. 3. Tumidopteris astra sp. nov., holotype GIN 4851/343h, morphology of sori. a: part of fertile pinnule; b: one practically complete sorus located on the terminal part of a lateral vein; c: sorus with four visible sporangia; d: partly damaged sorus with three visible sporangia; e: two neighbouring sori. Locality: the borehole IK-675, depth 961.7 m. Scale 1 mm (a, b, e), 500 Μm (c), 100 Μm (d).
Text-fig. 2. Tumidopteris astra sp. nov., macromorphology. a, c: sterile pinna, spec. GIN 4851/340; b, d: holotype GIN 4851/343h; e: sterile pinna, spec. GIN 4851/344. Localities: the city of Vorkuta, Section 49, layer 254 (a, c), the borehole IK-675, depth 961.7 m (b, d), the borehole IK-677, depth 147.8 m (e). Scale 1 cm (a, b, c, e), 1 mm (d). in A New Species Of The Genus Tumidopteris Naugolnykh From The Permian Of The Pechora Cis-Urals, Russia
Text-fig. 2. Tumidopteris astra sp. nov., macromorphology. a, c: sterile pinna, spec. GIN 4851/340; b, d: holotype GIN 4851/343h; e: sterile pinna, spec. GIN 4851/344. Localities: the city of Vorkuta, Section 49, layer 254 (a, c), the borehole IK-675, depth 961.7 m (b, d), the borehole IK-677, depth 147.8 m (e). Scale 1 cm (a, b, c, e), 1 mm (d).
Text-fig. 6. Comparative analysis of the three genera (Prynadaeopteris RADCZ., Geperapteris S.V.MEYEN, Tumidopteris NAUGOLNYKH) with possible affinity to Gleicheniaceae from the Permian deposits of Angaraland. a–c: Tumidopteris NAUGOLNYKH; d–f: Prynadaeopteris RADCZ. (based on Radczenko 1955, 1956, Naugolnykh 2013); g–i: Geperapteris S.V.MEYEN (based on Meyen 1982, Naugolnykh 2013). Left column – sori in plan (frontal view); central column – leaves; right column – sori in cross-section; FL – flattened sori; HS – hemispherical sori. Scale 1 cm (b, h), 5 mm (e), 1 mm (a, d), 0.5 mm (g); c, f, i – figures schematically drawn without scale. in A New Species Of The Genus Tumidopteris Naugolnykh From The Permian Of The Pechora Cis-Urals, Russia
Text-fig. 6. Comparative analysis of the three genera (Prynadaeopteris RADCZ., Geperapteris S.V.MEYEN, Tumidopteris NAUGOLNYKH) with possible affinity to Gleicheniaceae from the Permian deposits of Angaraland. a–c: Tumidopteris NAUGOLNYKH; d–f: Prynadaeopteris RADCZ. (based on Radczenko 1955, 1956, Naugolnykh 2013); g–i: Geperapteris S.V.MEYEN (based on Meyen 1982, Naugolnykh 2013). Left column – sori in plan (frontal view); central column – leaves; right column – sori in cross-section; FL – flattened sori; HS – hemispherical sori. Scale 1 cm (b, h), 5 mm (e), 1 mm (a, d), 0.5 mm (g); c, f, i – figures schematically drawn without scale.
Text-fig. 3. Scanning electron microscope (SEM) images of a charalean oospore (a), and fragments of probable marchantialean liverwort thalli (b–d); Torres Vedras locality, Portugal. a) Apical view of oospore showing the pattern of spiral ridges and grooves resulting from the enclosing cells of the oogonium. b–d) Thallus fragments in probable ventral view showing two rows of imbricate scales and occasional branching of the thallus (d). Specimens, TV38-S174607 (a), TV43-S174655 (b), TV43-S174654 (c), TV43-S174661 (d). Scale bars 1 mm (b–d), 100 Μm (a). in The Early Cretaceous Mesofossil Flora Of Torres Vedras (Ne Of Forte Da Forca), Portugal: A Palaeofloristic Analysis Of An Early Angiosperm Community
Text-fig. 3. Scanning electron microscope (SEM) images of a charalean oospore (a), and fragments of probable marchantialean liverwort thalli (b–d); Torres Vedras locality, Portugal. a) Apical view of oospore showing the pattern of spiral ridges and grooves resulting from the enclosing cells of the oogonium. b–d) Thallus fragments in probable ventral view showing two rows of imbricate scales and occasional branching of the thallus (d). Specimens, TV38-S174607 (a), TV43-S174655 (b), TV43-S174654 (c), TV43-S174661 (d). Scale bars 1 mm (b–d), 100 Μm (a).
Text-fig. 10. Scanning electron microscope (SEM) images of conifer seeds (a, b) and pollen (c) and monoporate pollen of unknown affinity (d–j); Torres Vedras locality, Portugal. a, b) Unnamed conifer seeds (conifer seed sp. 1); c) Clump of bisaccate pollen grains; d) Fragment with microsporangia that yielded the pollen in (e–j); e, f, h) Monoporate pollen grains folded in various ways, exposing the tiny pore (e, h, arrowheads) or resembling a monocolpate grain (f); g) Detail of pollen grain showing pore (arrowhead) and finely rugulate exine surface that reflects the reticulate infratectal layer beneath the thin tectum; i) Detail of pore showing very slightly thickened margin; j) Spherical orbicules on the surface of two grains. Specimens, TV44-S174594 (a), TV44-S174595 (b), TV44-S174573 (c), TV44-S137904 (d–j). Scale bars 1 mm (a, b), 300 Μm (d), 100 Μm (c), 6 Μm (e, f, h), 3 Μm (g, j), 1.5 Μm (i). in The Early Cretaceous Mesofossil Flora Of Torres Vedras (Ne Of Forte Da Forca), Portugal: A Palaeofloristic Analysis Of An Early Angiosperm Community
Text-fig. 10. Scanning electron microscope (SEM) images of conifer seeds (a, b) and pollen (c) and monoporate pollen of unknown affinity (d–j); Torres Vedras locality, Portugal. a, b) Unnamed conifer seeds (conifer seed sp. 1); c) Clump of bisaccate pollen grains; d) Fragment with microsporangia that yielded the pollen in (e–j); e, f, h) Monoporate pollen grains folded in various ways, exposing the tiny pore (e, h, arrowheads) or resembling a monocolpate grain (f); g) Detail of pollen grain showing pore (arrowhead) and finely rugulate exine surface that reflects the reticulate infratectal layer beneath the thin tectum; i) Detail of pore showing very slightly thickened margin; j) Spherical orbicules on the surface of two grains. Specimens, TV44-S174594 (a), TV44-S174595 (b), TV44-S174573 (c), TV44-S137904 (d–j). Scale bars 1 mm (a, b), 300 Μm (d), 100 Μm (c), 6 Μm (e, f, h), 3 Μm (g, j), 1.5 Μm (i).
Text-fig. 17. Scatter diagram of length and width of Promephitis species from Late Miocene faunas of southern Europe and western Asia. a – Promephitis maeotica, p4, dex, Gaverdovsky, GIN-1144-301: labial (left) and lingual (right) views. b – P. maeotica, p4, sin, reversed, Novoelizavetovka, PIN-355: labial (left) and lingual (right) views. Scale 1 mm. in Late Miocene (Early Turolian) Vertebrate Faunas And Associated Biotic Record Of The Northern Caucasus: Geology, Taxonomy, Palaeoenvironment, Biochronology
Text-fig. 17. Scatter diagram of length and width of Promephitis species from Late Miocene faunas of southern Europe and western Asia. a – Promephitis maeotica, p4, dex, Gaverdovsky, GIN-1144-301: labial (left) and lingual (right) views. b – P. maeotica, p4, sin, reversed, Novoelizavetovka, PIN-355: labial (left) and lingual (right) views. Scale 1 mm.
Text-fig. 8. Tarsometatarsi of fossil and Recent Sylvioidea. a – PIN, № 5528/3 from Volchaya Balka; b – PIN № 5528/4 from Volchaya Balka; c – Sylvia intermedia KESSLER, 2013; d – Sylvia borin (BODDAERT, 1783). a1–d1 – dorsal view; a2–d2 – plantar view; a3–d3 – distal view. Scale bars 1 mm. in Late Miocene (Early Turolian) Vertebrate Faunas And Associated Biotic Record Of The Northern Caucasus: Geology, Taxonomy, Palaeoenvironment, Biochronology
Text-fig. 8. Tarsometatarsi of fossil and Recent Sylvioidea. a – PIN, № 5528/3 from Volchaya Balka; b – PIN № 5528/4 from Volchaya Balka; c – Sylvia intermedia KESSLER, 2013; d – Sylvia borin (BODDAERT, 1783). a1–d1 – dorsal view; a2–d2 – plantar view; a3–d3 – distal view. Scale bars 1 mm.
Text-fig. 7. Fossil urodelans from studied localities. a, b – Mioproteus caucasicus, trunk vertebra, dorsal (a) and lateral (b) views; c, d – Chelotriton paradoxus, trunk vertebra, dorsal (c) and lateral (d) view. Scale bar 1 mm. in Late Miocene (Early Turolian) Vertebrate Faunas And Associated Biotic Record Of The Northern Caucasus: Geology, Taxonomy, Palaeoenvironment, Biochronology
Text-fig. 7. Fossil urodelans from studied localities. a, b – Mioproteus caucasicus, trunk vertebra, dorsal (a) and lateral (b) views; c, d – Chelotriton paradoxus, trunk vertebra, dorsal (c) and lateral (d) view. Scale bar 1 mm.
Text-fig. 19. ONHM TQ 15, right P4/ of a palaeomastodontoid from Taqah, Dhofar Governorate, Oman. a) stereo radicular view, b) stereo occlusal view (scale bar 10 mm). in Large Mammals From The Rupelian Of Oman - Recent Finds
Text-fig. 19. ONHM TQ 15, right P4/ of a palaeomastodontoid from Taqah, Dhofar Governorate, Oman. a) stereo radicular view, b) stereo occlusal view (scale bar 10 mm).
Text-fig. 12. Lower molars of (a) Omanitherium dhofarense and (b) Moeritherium chehbeurameuri. a) stereo occlusal views of ONHM TN 2017-50, posterior lophid of an unworn right lower molar, probably m/2, from Mohammed's molar site, Dhofar, Oman, b) stereo occlusal views of MNHN 1890-14, left lower molar from "Khenchella", Algeria (note the longitudinal sulcus in the centre-line of the tooth of Moeritherium and its absence in Omanitherium). Arrows show the course of the sulcus in the molar from "Khenchella" (scale bar 10 mm). in Large Mammals From The Rupelian Of Oman - Recent Finds
Text-fig. 12. Lower molars of (a) Omanitherium dhofarense and (b) Moeritherium chehbeurameuri. a) stereo occlusal views of ONHM TN 2017-50, posterior lophid of an unworn right lower molar, probably m/2, from Mohammed's molar site, Dhofar, Oman, b) stereo occlusal views of MNHN 1890-14, left lower molar from "Khenchella", Algeria (note the longitudinal sulcus in the centre-line of the tooth of Moeritherium and its absence in Omanitherium). Arrows show the course of the sulcus in the molar from "Khenchella" (scale bar 10 mm).
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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.