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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.

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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).

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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).

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Text-fig. 5. Scanning electron micrographs (d–g) and synchrotron radiation X-ray tomographic microscopy orthoslices (a–c) of flowers of Atlantocarpus virginiensis gen. et sp. nov. (a–d: holotype, PP43780, Puddledock sample 156), Atlantocarpus sp. from the Early Cretaceous Buarcos locality (e, f: S105025, Buarcos sample 244) and receptacle of Atlantocarpus? from the Early Cretaceous Vale de Água locality (g: S101300, Vale de Água sample 141). a) Flower in lateral view showing scar from a single bract (br), attachment scars of tepals (t) and stamens (st) on the expanded basal portion of elongated receptacle and young carpels; b) Flower in lateral view showing expanded basal portion of the elongated receptacle and young carpels; c) Flower in longitudinal section showing expanded basal portion of the elongated receptacle and young carpels; note the irregular, possibly expanded stigmatic region (arrow heads), (orthoslice yz0340); d) Flower in lateral view showing attachment scars of tepals (t) and stamens (st) on the expanded basal portion of elongated receptacle and young carpels with possible grooved stigmatic regions (arrow heads); e) Flower in lateral view showing expanded basal portion of elongated receptacle and young carpels; f) Detail of flower in (e) showing in Multiparted, Apocarpous Flowers From The Early Cretaceous Of Eastern North America And Portugal

Text-fig. 5. Scanning electron micrographs (d–g) and synchrotron radiation X-ray tomographic microscopy orthoslices (a–c) of flowers of Atlantocarpus virginiensis gen. et sp. nov. (a–d: holotype, PP43780, Puddledock sample 156), Atlantocarpus sp. from the Early Cretaceous Buarcos locality (e, f: S105025, Buarcos sample 244) and receptacle of Atlantocarpus? from the Early Cretaceous Vale de Água locality (g: S101300, Vale de Água sample 141). a) Flower in lateral view showing scar from a single bract (br), attachment scars of tepals (t) and stamens (st) on the expanded basal portion of elongated receptacle and young carpels; b) Flower in lateral view showing expanded basal portion of the elongated receptacle and young carpels; c) Flower in longitudinal section showing expanded basal portion of the elongated receptacle and young carpels; note the irregular, possibly expanded stigmatic region (arrow heads), (orthoslice yz0340); d) Flower in lateral view showing attachment scars of tepals (t) and stamens (st) on the expanded basal portion of elongated receptacle and young carpels with possible grooved stigmatic regions (arrow heads); e) Flower in lateral view showing expanded basal portion of elongated receptacle and young carpels; f) Detail of flower in (e) showing

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Text-fig. 4. Synchrotron radiation X-ray tomographic microscopy orthoslices of flowers of Lambertiflora virginiense gen. et sp. nov. from the Early Cretaceous Puddledock locality, Virginia, USA (holotype, PP53796, Puddledock sample 081). White dots – tepals, yellow dots – stamens or staminodes, red dot – central conical gynoecial region. a) Flower in longitudinal section showing elongated overlapping tepals, remains of probable poorly developed stamens or staminodes and probable poorly developed carpels on the central conical gynoecial region of the receptacle (orthoslice yz0454); b) Flower in transverse section showing rhomboidal bases of 30 tepals, nine poorly developed stamens or staminodes, and the central poorly differentiated gynoecial region of the receptacle (orthoslice xy1160); c) Flower in transverse section at the level of the floral receptacle showing 30 tepals, nine of the poorly developed stamens or staminodes, and the central poorly differentiated gynoecial region of the receptacle (orthoslice xy1250). Scale bars = 250 µm (a–c). in Multiparted, Apocarpous Flowers From The Early Cretaceous Of Eastern North America And Portugal

Text-fig. 4. Synchrotron radiation X-ray tomographic microscopy orthoslices of flowers of Lambertiflora virginiense gen. et sp. nov. from the Early Cretaceous Puddledock locality, Virginia, USA (holotype, PP53796, Puddledock sample 081). White dots – tepals, yellow dots – stamens or staminodes, red dot – central conical gynoecial region. a) Flower in longitudinal section showing elongated overlapping tepals, remains of probable poorly developed stamens or staminodes and probable poorly developed carpels on the central conical gynoecial region of the receptacle (orthoslice yz0454); b) Flower in transverse section showing rhomboidal bases of 30 tepals, nine poorly developed stamens or staminodes, and the central poorly differentiated gynoecial region of the receptacle (orthoslice xy1160); c) Flower in transverse section at the level of the floral receptacle showing 30 tepals, nine of the poorly developed stamens or staminodes, and the central poorly differentiated gynoecial region of the receptacle (orthoslice xy1250). Scale bars = 250 µm (a–c).

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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).

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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.

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Text-fig. 50. Scanning electron microscope (SEM) and synchrotron radiation X-ray tomographic microscopy (SRXTM) images of a flower and mature carpels of Reyanthus lusitanicus gen. et sp. nov.; Torres Vedras locality, Portugal. a) Holotype; multicarpellate flower showing numerous carpels surrounded by remains of the androecium and perianth; note the bract subtending the flower (arrowhead); b, c) Longitudinal sections perpendicular to section in (f) (b, SRXTM orthoslice xz0461) and (c, SRXTM cut voltex xz0540-0580) showing receptacle, carpels and remains of the androecium and perianth; note prominent cavities formed by the oil cells, subtending bract (arrow) and bract subtending fragmentary bud (arrowhead); d, e) Apical (d) and lateral (e) views of gynoecium showing laterally flattened carpels and dorsi-ventrally flattened stamen or staminode (* in e); f) Longitudinal section (SRXTM orthoslice yz0405) of gynoecium showing conical receptacle and carpels with densely spaced oil cells; g, h) Mature carpel of Reyanthus lusitanicus gen. et sp. nov. showing slightly curved form, rounded apex and base that tapers toward the attachment to the receptacle; i) Surface of carpel showing embedded oil cells; j) Transverse section through three carpels showing attachment of developing ovules near the ventral sutures and oil cells in the wall just below the surface (SRXTM cut voltex xy0770-0845). Specimens TV299-S136716 (holotype; a–f), TV299-S136717 (g–j). Scale bars 300 Μm (a–d, f–h), 150 Μm (e, j), 30 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. 50. Scanning electron microscope (SEM) and synchrotron radiation X-ray tomographic microscopy (SRXTM) images of a flower and mature carpels of Reyanthus lusitanicus gen. et sp. nov.; Torres Vedras locality, Portugal. a) Holotype; multicarpellate flower showing numerous carpels surrounded by remains of the androecium and perianth; note the bract subtending the flower (arrowhead); b, c) Longitudinal sections perpendicular to section in (f) (b, SRXTM orthoslice xz0461) and (c, SRXTM cut voltex xz0540-0580) showing receptacle, carpels and remains of the androecium and perianth; note prominent cavities formed by the oil cells, subtending bract (arrow) and bract subtending fragmentary bud (arrowhead); d, e) Apical (d) and lateral (e) views of gynoecium showing laterally flattened carpels and dorsi-ventrally flattened stamen or staminode (* in e); f) Longitudinal section (SRXTM orthoslice yz0405) of gynoecium showing conical receptacle and carpels with densely spaced oil cells; g, h) Mature carpel of Reyanthus lusitanicus gen. et sp. nov. showing slightly curved form, rounded apex and base that tapers toward the attachment to the receptacle; i) Surface of carpel showing embedded oil cells; j) Transverse section through three carpels showing attachment of developing ovules near the ventral sutures and oil cells in the wall just below the surface (SRXTM cut voltex xy0770-0845). Specimens TV299-S136716 (holotype; a–f), TV299-S136717 (g–j). Scale bars 300 Μm (a–d, f–h), 150 Μm (e, j), 30 Μm (i).

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Text-fig. 31. Scanning electron microscope (SEM) images of monocolpate pollen of Burgeria striata gen. et sp. nov. from a pollen clump; Torres Vedras locality, Portugal. a) Holotype; pollen clump that yielded the pollen in this Text-figure; b) Pollen grains showing the distal colpus and the undulating tectum perforated by scattered punctae; c–e) Equatorial (c) and distal views (d, e) of pollen grains showing the long distal colpus with granular ornamentation and the undulating tectum perforated by scattered punctae; f) Detail of section through pollen wall showing thick tectum with fine striate ornamentation, perforated by punctae and supported by short stout columellae attached to the thin foot layer; g–h) Surface of tectum (g) and orbicule (h) showing fine striate ornamentation. Specimen, TV44-S149216 (holotype). Scale bars 300 Μm (a), 30 Μm (b), 6 Μm (c–e), 1.5 Μm (f–h). 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. 31. Scanning electron microscope (SEM) images of monocolpate pollen of Burgeria striata gen. et sp. nov. from a pollen clump; Torres Vedras locality, Portugal. a) Holotype; pollen clump that yielded the pollen in this Text-figure; b) Pollen grains showing the distal colpus and the undulating tectum perforated by scattered punctae; c–e) Equatorial (c) and distal views (d, e) of pollen grains showing the long distal colpus with granular ornamentation and the undulating tectum perforated by scattered punctae; f) Detail of section through pollen wall showing thick tectum with fine striate ornamentation, perforated by punctae and supported by short stout columellae attached to the thin foot layer; g–h) Surface of tectum (g) and orbicule (h) showing fine striate ornamentation. Specimen, TV44-S149216 (holotype). Scale bars 300 Μm (a), 30 Μm (b), 6 Μm (c–e), 1.5 Μm (f–h).

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Text-fig. 22. Scanning electron microscope (SEM) images of fragmentary stamens (a, b) with in situ pollen of Clavatipollenites sp. 1 (c–g); Torres Vedras locality, Portugal. a, b) Fragmentary tetrasporangiate stamens; c–e) Distal view of pollen grains showing large, rounded aperture and the irregular verrucate aperture membrane; f) Proximal view of pollen grains showing dense reticulum; g) Section through the fractured pollen wall showing foot layer, columellae and muri with faint supratectal ornamentation. Specimens, TV44-S105013 (a, c, d), TV44-S105019 (b, e–g). Scale bars 300 Μm (a, b), 6 Μm (c–f), 3 Μm (g). 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. 22. Scanning electron microscope (SEM) images of fragmentary stamens (a, b) with in situ pollen of Clavatipollenites sp. 1 (c–g); Torres Vedras locality, Portugal. a, b) Fragmentary tetrasporangiate stamens; c–e) Distal view of pollen grains showing large, rounded aperture and the irregular verrucate aperture membrane; f) Proximal view of pollen grains showing dense reticulum; g) Section through the fractured pollen wall showing foot layer, columellae and muri with faint supratectal ornamentation. Specimens, TV44-S105013 (a, c, d), TV44-S105019 (b, e–g). Scale bars 300 Μm (a, b), 6 Μm (c–f), 3 Μm (g).

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Text-fig. 24. Scanning electron microscope (SEM) images (a, c, d) and synchrotron radiation X-ray tomographic microscopy (SRXTM) images (b, e) of fruits and seeds of Serialis antiqua (a, b) and Serialis parva (c–e); Torres Vedras locality, Portugal. a, b) Serialis antiqua lateral view of fruit showing smooth partly abraded fruit wall (a) and longitudinal section (b, SRXTM orthoslice yz0862) showing six closely adhering seeds, some of which are mature with well-preserved nutritive tissue; c–e) Serialis parva lateral view of fruit showing faint ribs (c), finely pitted seed surface with undulate anticlinal walls of the exotestal cells (d), and transverse section showing two closely adhering seeds (SRXTM orthoslice xy0913, e). Specimens, TV43-S174480 (a, b), TV43-S170076 (c), TV43-S170079 (d), TV43-S174477 (e). Scale bars 300 Μm (a–c, e), 50 Μm (d). 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. 24. Scanning electron microscope (SEM) images (a, c, d) and synchrotron radiation X-ray tomographic microscopy (SRXTM) images (b, e) of fruits and seeds of Serialis antiqua (a, b) and Serialis parva (c–e); Torres Vedras locality, Portugal. a, b) Serialis antiqua lateral view of fruit showing smooth partly abraded fruit wall (a) and longitudinal section (b, SRXTM orthoslice yz0862) showing six closely adhering seeds, some of which are mature with well-preserved nutritive tissue; c–e) Serialis parva lateral view of fruit showing faint ribs (c), finely pitted seed surface with undulate anticlinal walls of the exotestal cells (d), and transverse section showing two closely adhering seeds (SRXTM orthoslice xy0913, e). Specimens, TV43-S174480 (a, b), TV43-S170076 (c), TV43-S170079 (d), TV43-S174477 (e). Scale bars 300 Μm (a–c, e), 50 Μm (d).

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Text-fig. 20. Scanning electron microscope (SEM) images of fruits of Hedyflora (a–d), stamen with in situ Asteropollis sp. pollen (e–g), and Hedyosmum-like staminate inflorescence (h); Torres Vedras locality, Portugal. a, b) Hedyflora sp. 1, lateral and apical views of fruits showing the triangular cross-section, remains of three tepals, apical style and the three lateral "windows" in the hypanthium; c, d) Hedyflora sp. 2, lateral views of fruits showing three well-preserved tepals, apical style and the lateral "windows" in the hypanthium; note the papillae on the lateral wall and around the base of the style; e, f, g) Stamen (f) with in situ pollen of Asteropollis sp. showing the poorly defined star-shaped apertural area (e) and reticulate tectum, with the muri ornamented by small verrucae (g); h) Hedyosmum-like staminate inflorescence with five whorls of tetrasporangiate stamens. Specimens, TV43-S101749 (a, b), TV43-S101307 (c, d), TV44-S137917 (e–g), TV39-S101220 (h). Scale bars 300 Μm (a–d, f, h), 6 Μm (e), 1.5 Μm (g). 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. 20. Scanning electron microscope (SEM) images of fruits of Hedyflora (a–d), stamen with in situ Asteropollis sp. pollen (e–g), and Hedyosmum-like staminate inflorescence (h); Torres Vedras locality, Portugal. a, b) Hedyflora sp. 1, lateral and apical views of fruits showing the triangular cross-section, remains of three tepals, apical style and the three lateral "windows" in the hypanthium; c, d) Hedyflora sp. 2, lateral views of fruits showing three well-preserved tepals, apical style and the lateral "windows" in the hypanthium; note the papillae on the lateral wall and around the base of the style; e, f, g) Stamen (f) with in situ pollen of Asteropollis sp. showing the poorly defined star-shaped apertural area (e) and reticulate tectum, with the muri ornamented by small verrucae (g); h) Hedyosmum-like staminate inflorescence with five whorls of tetrasporangiate stamens. Specimens, TV43-S101749 (a, b), TV43-S101307 (c, d), TV44-S137917 (e–g), TV39-S101220 (h). Scale bars 300 Μm (a–d, f, h), 6 Μm (e), 1.5 Μm (g).

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Text-fig. 15. Scanning electron microscope (SEM) images of seeds of Pazliopsis reyi (a–c) and Anaspermum operculatum gen. et sp. nov. (d–j). a) Seed in lateral view showing poorly preserved remains of fruit wall and rough surface of the exotesta; b) Section through the wall of a broken seed showing palisade cells of the exotesta; c) Seed surface showing sunken very deeply sinuous outlines of the exotesta cells; d–f, h, i) Seeds in lateral view (holotype figured in d) showing the pointed micropylar-hilar area, the rounded chalazal end, the smooth surface of the exotesta composed of cells with sinuous cell outlines, and the distinct course of the raphe; g) Surface of the exotesta showing the distinctive cell outlines formed by the sinuous anticlinal walls of the palisade cells; j) Apical view of seed showing the prominent operculum. Specimens, TV43-S171534 (a), TV44-S136683 (b), TV43-S136745 (c), TV43-S136740 (holotype; d), TV43-S136746 (e), TV43-S136739 (f), TV43-S170083 (g), TV S136743 (h), TV43-S136742 (i), TV38-S174608 (j). Scale bars 300 Μm (a, b, d–f, h, i), 50 Μm (j), 30 Μm (c, g). 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. 15. Scanning electron microscope (SEM) images of seeds of Pazliopsis reyi (a–c) and Anaspermum operculatum gen. et sp. nov. (d–j). a) Seed in lateral view showing poorly preserved remains of fruit wall and rough surface of the exotesta; b) Section through the wall of a broken seed showing palisade cells of the exotesta; c) Seed surface showing sunken very deeply sinuous outlines of the exotesta cells; d–f, h, i) Seeds in lateral view (holotype figured in d) showing the pointed micropylar-hilar area, the rounded chalazal end, the smooth surface of the exotesta composed of cells with sinuous cell outlines, and the distinct course of the raphe; g) Surface of the exotesta showing the distinctive cell outlines formed by the sinuous anticlinal walls of the palisade cells; j) Apical view of seed showing the prominent operculum. Specimens, TV43-S171534 (a), TV44-S136683 (b), TV43-S136745 (c), TV43-S136740 (holotype; d), TV43-S136746 (e), TV43-S136739 (f), TV43-S170083 (g), TV S136743 (h), TV43-S136742 (i), TV38-S174608 (j). Scale bars 300 Μm (a, b, d–f, h, i), 50 Μm (j), 30 Μm (c, g).

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Text-fig. 17. Scanning electron microscope (SEM) and synchrotron radiation X-ray tomographic microscopy (SRXTM) images of a fruit of Canrightia elongata sp. nov. (a–g) and isolated Canrightia-like seeds (h–j); Torres Vedras locality, Portugal. a–c) Holotype; fruit in lateral view showing four fused tepals at the base (c, upper arrowheads) and prominent cavities in the fruit wall formed by scattered oil bodies and possible subtending bract (c, lower arrowhead); d) Transverse section (SRXTM orthoslice xy1510) through the fruit showing three locules, one with the remains of the endothelium (top left, 1), the other two (2, 3) with remains of presumed endosperm tissue; note that the locule to the right (3) is crushed; e, f) Radial longitudinal (e; SRXTM orthoslice xz1212) 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. 17. Scanning electron microscope (SEM) and synchrotron radiation X-ray tomographic microscopy (SRXTM) images of a fruit of Canrightia elongata sp. nov. (a–g) and isolated Canrightia-like seeds (h–j); Torres Vedras locality, Portugal. a–c) Holotype; fruit in lateral view showing four fused tepals at the base (c, upper arrowheads) and prominent cavities in the fruit wall formed by scattered oil bodies and possible subtending bract (c, lower arrowhead); d) Transverse section (SRXTM orthoslice xy1510) through the fruit showing three locules, one with the remains of the endothelium (top left, 1), the other two (2, 3) with remains of presumed endosperm tissue; note that the locule to the right (3) is crushed; e, f) Radial longitudinal (e; SRXTM orthoslice xz1212)

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Text-fig. 14. Scanning electron microscope (SEM) and synchrotron radiation X-ray tomographic microscopy (SRXTM) images of seeds of Gastonispermum antiquum sp. nov. (a–e) and possible fruits (f–h); Torres Vedras locality, Portugal. a–c) Lateral view of seeds (holotype figured in b) showing the hilar-micropylar area and the course of the raphe; note the close association of hilum (arrowhead) and micropyle; d) Detail of seed wall showing the undulating surface of the exotesta composed of cells with sinuous cell outlines; e) Longitudinal section (orthoslice xy0914) through the hilar-micropylar area showing the hilum (arrowhead), the thickening of the endotesta around the micropyle and the course of the raphe within the exotesta (arrow); f–h) Fruits containing 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. 14. Scanning electron microscope (SEM) and synchrotron radiation X-ray tomographic microscopy (SRXTM) images of seeds of Gastonispermum antiquum sp. nov. (a–e) and possible fruits (f–h); Torres Vedras locality, Portugal. a–c) Lateral view of seeds (holotype figured in b) showing the hilar-micropylar area and the course of the raphe; note the close association of hilum (arrowhead) and micropyle; d) Detail of seed wall showing the undulating surface of the exotesta composed of cells with sinuous cell outlines; e) Longitudinal section (orthoslice xy0914) through the hilar-micropylar area showing the hilum (arrowhead), the thickening of the endotesta around the micropyle and the course of the raphe within the exotesta (arrow); f–h) Fruits containing

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Text-fig. 5. Palynomorphs from Late Miocene deposits. Gaverdovsky section, North Caucasus. a – Abies minor ANANOVA; b – Picea sp.; c – Keteleeria cf. dubia CHLONOWA; d – Taxodiaceae gen.; e – Podocarpidites podocarpoides (THIERGART) KRUTZSCH; f – Pinus labdaca KRUTZSCH; g – Fagus cf. tenella PAN.; h – Juglans gracilis ANANOVA; I – Carya cf. spackmania TRAV.; j – Pterocarya sp.; k – Ulmus sp.; l – Zelkova cf. miocenica ANANOVA; m – Liquidambar sp.; n – Pediastrum simplex MEYEN; o – Spirogyra sp.; p – redeposited Palaeogene dinocyst Wilsonidinium lineidentatum (DEFLANDRE et COOKSON, 1955) LENTIN et WILLIAMS, 1976. Scale bar 40 μm for all photographs. in Late Miocene (Early Turolian) Vertebrate Faunas And Associated Biotic Record Of The Northern Caucasus: Geology, Taxonomy, Palaeoenvironment, Biochronology

Text-fig. 5. Palynomorphs from Late Miocene deposits. Gaverdovsky section, North Caucasus. a – Abies minor ANANOVA; b – Picea sp.; c – Keteleeria cf. dubia CHLONOWA; d – Taxodiaceae gen.; e – Podocarpidites podocarpoides (THIERGART) KRUTZSCH; f – Pinus labdaca KRUTZSCH; g – Fagus cf. tenella PAN.; h – Juglans gracilis ANANOVA; I – Carya cf. spackmania TRAV.; j – Pterocarya sp.; k – Ulmus sp.; l – Zelkova cf. miocenica ANANOVA; m – Liquidambar sp.; n – Pediastrum simplex MEYEN; o – Spirogyra sp.; p – redeposited Palaeogene dinocyst Wilsonidinium lineidentatum (DEFLANDRE et COOKSON, 1955) LENTIN et WILLIAMS, 1976. Scale bar 40 μm for all photographs.

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Text-fig. 3. Correlation model of the studied sections of Late Miocene deposits. a. Tuapse highway bridge. b. Gaverdovsky. c. Volchaya Balka. 1. reversed polarity; 2. normal polarity; 3. unstudied interval. in Late Miocene (Early Turolian) Vertebrate Faunas And Associated Biotic Record Of The Northern Caucasus: Geology, Taxonomy, Palaeoenvironment, Biochronology

Text-fig. 3. Correlation model of the studied sections of Late Miocene deposits. a. Tuapse highway bridge. b. Gaverdovsky. c. Volchaya Balka. 1. reversed polarity; 2. normal polarity; 3. unstudied interval.

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Text-fig. 1. Geographic location of the studied sections. 1. Gaverdovsky, 2. Volchaya Balka, 3. Tuapse highway bridge, 4. Maikop city park. in Late Miocene (Early Turolian) Vertebrate Faunas And Associated Biotic Record Of The Northern Caucasus: Geology, Taxonomy, Palaeoenvironment, Biochronology

Text-fig. 1. Geographic location of the studied sections. 1. Gaverdovsky, 2. Volchaya Balka, 3. Tuapse highway bridge, 4. Maikop city park.

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Text-fig. 16. a) MNHN LBE 007, symphysis with left and right i/1 of Barytherium sp. from Dor el Talha, Libya. (a1 – superior stereo views of the symphysis, a2 – stereo distal view of right i/1 (arrow 1 shows the interstitial contact facet close to the apex caused by abrasion against the right i/2), a3 – section of right i/1 viewed from the radicular end to show the extent of the enamel cover (below the arrows 2) and the dome-shaped dentine mass on the lingual aspect (above the arrows), a4 – stereo occlusal views of right i/1 (note the orientation of the apical wear facet), a5 – stereo mesial view) (scale bar 5 cm); b–c) NHMUK M 82167b, distal stereo views of lower central incisors of Arcanotherium savagei from Dor el Talha, Libya, to show the interstitial wear facets near cervix caused by abrasion against the i/2s (b – left i/1, c – right i/1) (scale bar 10 cm). in Large Mammals From The Rupelian Of Oman - Recent Finds

Text-fig. 16. a) MNHN LBE 007, symphysis with left and right i/1 of Barytherium sp. from Dor el Talha, Libya. (a1 – superior stereo views of the symphysis, a2 – stereo distal view of right i/1 (arrow 1 shows the interstitial contact facet close to the apex caused by abrasion against the right i/2), a3 – section of right i/1 viewed from the radicular end to show the extent of the enamel cover (below the arrows 2) and the dome-shaped dentine mass on the lingual aspect (above the arrows), a4 – stereo occlusal views of right i/1 (note the orientation of the apical wear facet), a5 – stereo mesial view) (scale bar 5 cm); b–c) NHMUK M 82167b, distal stereo views of lower central incisors of Arcanotherium savagei from Dor el Talha, Libya, to show the interstitial wear facets near cervix caused by abrasion against the i/2s (b – left i/1, c – right i/1) (scale bar 10 cm).

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Text-fig. 5. Upper part of the stratigraphic section at the Omanitherium type locality. B–D correspond to the beds identified in the stratigraphic section (Text-fig. 3). The workers are excavating at the type locality. in Large Mammals From The Rupelian Of Oman - Recent Finds

Text-fig. 5. Upper part of the stratigraphic section at the Omanitherium type locality. B–D correspond to the beds identified in the stratigraphic section (Text-fig. 3). The workers are excavating at the type locality.

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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.

allen-brain-atlas
neuroscienceopenDocumentation, web resources, and API references are available online.
Last verified 2026-04-30Open record

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.

abode-home-cage
behavioral-neuroscienceopenThe DataShare record exposes download links for annotations, documentation, license text, and the zipped per-snippet data directory.
Last verified 2026-04-30Open record

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.

dandi-nwb
electrophysiologyopenPublished Dandiset metadata and archive endpoints are available through the production DANDI API.
Last verified 2026-04-30Open record

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.

ibl
behavioral-neuroscienceopenPublic sessions can be searched and loaded from the IBL public data server through ONE.
Last verified 2026-04-29Open record

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.

openneuro
neuroscienceopenPublished datasets are available on demand over the internet.
Last verified 2026-04-29Open record

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