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Text-fig. 8. Pterocaryoxylon sp., a–c, e: UF 279-85024; d, f: UF 279-24551. a, b: Wood semi-ring-porous, vessels solitary and in short radial multiples, axial parenchyma scanty vasicentric, marginal, and in narrow lines, TS. c: Crowded alternate intervessel pitting, simple perforation plate (PP), TLS. d: Vessel-axial parenchyma pitting similar to intervessel pitting, RLS. e: Rays mostly 1–3 cells wide, occasionally 4 cells, uniseriate rays probably mostly square to upright cells, TLS. f: Rays heterocellular, body cells procumbent. Scale bars: 200 µm in a, b; 100 µm in e, f; 50 µm in c; 20 µm in d. in A Diverse Assemblage Of Late Eocene Woods From Oregon, Western Usa
Text-fig. 8. Pterocaryoxylon sp., a–c, e: UF 279-85024; d, f: UF 279-24551. a, b: Wood semi-ring-porous, vessels solitary and in short radial multiples, axial parenchyma scanty vasicentric, marginal, and in narrow lines, TS. c: Crowded alternate intervessel pitting, simple perforation plate (PP), TLS. d: Vessel-axial parenchyma pitting similar to intervessel pitting, RLS. e: Rays mostly 1–3 cells wide, occasionally 4 cells, uniseriate rays probably mostly square to upright cells, TLS. f: Rays heterocellular, body cells procumbent. Scale bars: 200 µm in a, b; 100 µm in e, f; 50 µm in c; 20 µm in d.
Text-fig. 7. Hamamelidoxylon crystalliferum sp. nov., UF 279-34464. a: Diffuse porous wood with exclusively solitary vessels, tending to be angular in outline, TS. b: Growth ring boundary, marked by radially narrowed fibers, latewood vessels narrower than earlywood vessels of the next ring, fibers thick-walled, no axial parenchyma visible, TS. c: Scalariform intervessel pits in narrow vessel (left), fibers with distinctly bordered pits, TLS. d: Scalariform perforation plate, tyloses (T) formation from marginal ray cell, TLS. e: Scalariform perforation plates with fewer than 15 bars (PP), RLS. f: Vessel-ray parenchyma pits with in A Diverse Assemblage Of Late Eocene Woods From Oregon, Western Usa
Text-fig. 7. Hamamelidoxylon crystalliferum sp. nov., UF 279-34464. a: Diffuse porous wood with exclusively solitary vessels, tending to be angular in outline, TS. b: Growth ring boundary, marked by radially narrowed fibers, latewood vessels narrower than earlywood vessels of the next ring, fibers thick-walled, no axial parenchyma visible, TS. c: Scalariform intervessel pits in narrow vessel (left), fibers with distinctly bordered pits, TLS. d: Scalariform perforation plate, tyloses (T) formation from marginal ray cell, TLS. e: Scalariform perforation plates with fewer than 15 bars (PP), RLS. f: Vessel-ray parenchyma pits with
Text-fig. 1. Pistacia terrazasae sp. nov., a: UF 279-85025; b–i: UF 279-24545. a: Ring-porous wood with widely spaced solitary earlywood vessels; latewood vessels in radial multiples of 4 or more and in clusters, TS. b: Growth ring boundary, fiber walls thin to thick, TS. c: Simple perforation plates, alternate intervessel pits, helical thickenings in vessels, TLS. d: Multiseriate rays to 4-seriate, tyloses in vessels, helical thickenings throughout body of vessel element, and alternate intervessel pitting, TLS. e: Vessel-ray parenchyma pitting with reduced borders, oval in outline, RLS. f: Marginal row of upright cells, one inflated and crystalliferous, procumbent body cells, RLS. g: Multiseriate rays mostly 3-seriate, occasionally 4-seriate, uniseriate rays usually <10 cells tall, TLS. h: Ray with enlarged crystalliferous marginal cell, to left of C, TLS. i: Ray with canal, TLS. Scale bars: 200 µm in a, g; 100 µm in b, d, h; 50 µm in c, i; 20 µm in e, f. in A Diverse Assemblage Of Late Eocene Woods From Oregon, Western Usa
Text-fig. 1. Pistacia terrazasae sp. nov., a: UF 279-85025; b–i: UF 279-24545. a: Ring-porous wood with widely spaced solitary earlywood vessels; latewood vessels in radial multiples of 4 or more and in clusters, TS. b: Growth ring boundary, fiber walls thin to thick, TS. c: Simple perforation plates, alternate intervessel pits, helical thickenings in vessels, TLS. d: Multiseriate rays to 4-seriate, tyloses in vessels, helical thickenings throughout body of vessel element, and alternate intervessel pitting, TLS. e: Vessel-ray parenchyma pitting with reduced borders, oval in outline, RLS. f: Marginal row of upright cells, one inflated and crystalliferous, procumbent body cells, RLS. g: Multiseriate rays mostly 3-seriate, occasionally 4-seriate, uniseriate rays usually <10 cells tall, TLS. h: Ray with enlarged crystalliferous marginal cell, to left of C, TLS. i: Ray with canal, TLS. Scale bars: 200 µm in a, g; 100 µm in b, d, h; 50 µm in c, i; 20 µm in e, f.
Text-fig. 4. Fagus dodgei sp. nov., a, b, d–h: UF 279-34468; c: UF 279-30165. a: Wood diffuse-porous to semi-ring-porous with distinct latewood zone with narrower vessels; vessels solitary and in short multiples; diffuse, diffuse-in-aggregates axial parenchyma visible in latewood, TS. b: Growth ring boundary, TS. c: Opposite intervessel pitting, TLS. d: Scalariform perforation plate with fewer than 10 bars, RLS. e: Simple perforation plates (PP), RLS. f: Vessel-ray parenchyma pitting with reduced borders and frequently oval in outline, RLS. g: Rays 1–4(–5)-seriate with variable numbers of marginal rows, TLS. h: Rays of two distinct sizes, widest rays>10-seriate, TLS. Scale bars: 200 µm in a, h; 100 µm in b, e, g; 50 µm in d, f. in A Diverse Assemblage Of Late Eocene Woods From Oregon, Western Usa
Text-fig. 4. Fagus dodgei sp. nov., a, b, d–h: UF 279-34468; c: UF 279-30165. a: Wood diffuse-porous to semi-ring-porous with distinct latewood zone with narrower vessels; vessels solitary and in short multiples; diffuse, diffuse-in-aggregates axial parenchyma visible in latewood, TS. b: Growth ring boundary, TS. c: Opposite intervessel pitting, TLS. d: Scalariform perforation plate with fewer than 10 bars, RLS. e: Simple perforation plates (PP), RLS. f: Vessel-ray parenchyma pitting with reduced borders and frequently oval in outline, RLS. g: Rays 1–4(–5)-seriate with variable numbers of marginal rows, TLS. h: Rays of two distinct sizes, widest rays>10-seriate, TLS. Scale bars: 200 µm in a, h; 100 µm in b, e, g; 50 µm in d, f.
Text-fig. 2. Celtis popsii sp. nov., UF 279-34460. a: Growth ring with earlywood of multiple rows of vessels solitary and in radial multiples; latewood vessels in wavy tangential bands, TS. b: Growth ring boundary, latewood vessels in multiples with axial parenchyma confluent, TS. c: Simple perforation plates, alternate intervessel pits, polygonal in outline, TLS. d: Vessel-ray parenchyma pits to right of VRP, oval in outline, with slightly reduced borders, RLS. e: Rays tending to two sizes, some multiseriate rays with distinct sheath cells, multiseriate rays usually with 1 marginal row of square to upright cells, occasionally with 4 or more; uniseriate rays less than 10 cells high, TLS. f: Detail of multiseriate ray with distinct sheath cells, vessel element end walls, TLS. Scale bars: 200 µm in a, e; 100 µm in b; 50 µm in c, f; 20 µm in d. in A Diverse Assemblage Of Late Eocene Woods From Oregon, Western Usa
Text-fig. 2. Celtis popsii sp. nov., UF 279-34460. a: Growth ring with earlywood of multiple rows of vessels solitary and in radial multiples; latewood vessels in wavy tangential bands, TS. b: Growth ring boundary, latewood vessels in multiples with axial parenchyma confluent, TS. c: Simple perforation plates, alternate intervessel pits, polygonal in outline, TLS. d: Vessel-ray parenchyma pits to right of VRP, oval in outline, with slightly reduced borders, RLS. e: Rays tending to two sizes, some multiseriate rays with distinct sheath cells, multiseriate rays usually with 1 marginal row of square to upright cells, occasionally with 4 or more; uniseriate rays less than 10 cells high, TLS. f: Detail of multiseriate ray with distinct sheath cells, vessel element end walls, TLS. Scale bars: 200 µm in a, e; 100 µm in b; 50 µm in c, f; 20 µm in d.
Text-fig. 4. a: Conglomeratic to massive sandstone facies 1, facies A are composed of Andesit (AF), Clay (CF) and Sandstone (SF) fragments lain on medium-sandstone. b: Conglomeratic to massive sandstone facies, outcropping of massive sandstone facies comprises of fine to medium grain size of grey to yellowish sandstone. c: Heterolithic sandstone-mudstone facies, intercalation of fine sand with silt and shale as type form of heterolithic sandstone mudstone as indicated by a high sand/shale ratio. d: Example outcrops of heterolithic sandstone-mudstone 2 indicated by low sand/shale ratio. e: Heterolithic fine sand and mudstone and mudstone facies, intercalation of thin sandstone and shale. f: Representative of slump deposits outcrops belong to conglomeratic to massive sandstone facies, which is indicated by the intercalation of sandstone and shale and some disturbed beds or layers as seen in slump deposits. The facies type is normally deposited within the basin floor, channel margin or as a product of the overbank deposits. In this figure the slump deposit is shown as internal bedding, some occurred on the bedding-plane. Trend slope measurement of the fold-axis revealed values N 135°E and N 108°E. in Lithofacies And Ichnofacies Of Turbidite Deposits, West Java, Indonesia
Text-fig. 4. a: Conglomeratic to massive sandstone facies 1, facies A are composed of Andesit (AF), Clay (CF) and Sandstone (SF) fragments lain on medium-sandstone. b: Conglomeratic to massive sandstone facies, outcropping of massive sandstone facies comprises of fine to medium grain size of grey to yellowish sandstone. c: Heterolithic sandstone-mudstone facies, intercalation of fine sand with silt and shale as type form of heterolithic sandstone mudstone as indicated by a high sand/shale ratio. d: Example outcrops of heterolithic sandstone-mudstone 2 indicated by low sand/shale ratio. e: Heterolithic fine sand and mudstone and mudstone facies, intercalation of thin sandstone and shale. f: Representative of slump deposits outcrops belong to conglomeratic to massive sandstone facies, which is indicated by the intercalation of sandstone and shale and some disturbed beds or layers as seen in slump deposits. The facies type is normally deposited within the basin floor, channel margin or as a product of the overbank deposits. In this figure the slump deposit is shown as internal bedding, some occurred on the bedding-plane. Trend slope measurement of the fold-axis revealed values N 135°E and N 108°E.
Text-fig. 16. Photomicrographs of thin sections of specimen BP/16/1734, Terminalioxylon mozambicense sp. nov. from Mhengere Hill, Gorongosa, Mozambique. a: TS with round vessels, scanty paratracheal to vasicentric parenchyma, diffuse and narrow terminal or initial bands; b: TS at higher magnification, note the very narrow rays; c: TLS, vessels with small alternate pits, and partly tylosed; d–g: TLS with crystals (small white arrows) in the parenchyma cells, medium to thick-walled fibres and uniseriate, low rays; h: TLS, rays up to 20 cells high; i: RLS rays with procumbent body cells and 1–2 rows of marginal upright cells. in Stratigraphy, Chronology And Palaeontology Of The Tertiary Rocks Of The Cheringoma Plateau, Mozambique
Text-fig. 16. Photomicrographs of thin sections of specimen BP/16/1734, Terminalioxylon mozambicense sp. nov. from Mhengere Hill, Gorongosa, Mozambique. a: TS with round vessels, scanty paratracheal to vasicentric parenchyma, diffuse and narrow terminal or initial bands; b: TS at higher magnification, note the very narrow rays; c: TLS, vessels with small alternate pits, and partly tylosed; d–g: TLS with crystals (small white arrows) in the parenchyma cells, medium to thick-walled fibres and uniseriate, low rays; h: TLS, rays up to 20 cells high; i: RLS rays with procumbent body cells and 1–2 rows of marginal upright cells.
Text-fig. 10. Extant pans east of Inhaminga (18°26′28″'S: 35°35′45″E) surrounded by woodland. The pans typically have an arid, vegetation-free, marginal zone and a water-logged sump. Some pans are connected to each other by shallow overflow valleys. Image modified from Google Earth. in Stratigraphy, Chronology And Palaeontology Of The Tertiary Rocks Of The Cheringoma Plateau, Mozambique
Text-fig. 10. Extant pans east of Inhaminga (18°26′28″'S: 35°35′45″E) surrounded by woodland. The pans typically have an arid, vegetation-free, marginal zone and a water-logged sump. Some pans are connected to each other by shallow overflow valleys. Image modified from Google Earth.
Text-fig. 13. a, d–g: Acer aemilianum. b, c: Acer palmatum and A. sieboldianum modern leaves (NMNS Cleared Leaf Database). a: Oriolo MSF 661, 7-lobed leaf. b: Specimen U 1049, lobe detail showing finely serrate leaf margin. c: Specimen T 0246, 9-lobed leaf with coarsely serrate leaf margin. d: Oriolo MSF 645-1, 9-lobed leaf with two small additional lobes. e: Oriolo MSF 645. f: Oriolo MSF 660, 9-lobed specimen. g: Oriolo MSF 660-1. White arrows indicate position along lamina lobes where marginal serration starts. Scale bars 10 mm (a–c, f, g), 50 mm (d, e). in The Late Early Pleistocene Flora Of Oriolo, Faenza (Italy): Assembly Of The Modern Forest Biome
Text-fig. 13. a, d–g: Acer aemilianum. b, c: Acer palmatum and A. sieboldianum modern leaves (NMNS Cleared Leaf Database). a: Oriolo MSF 661, 7-lobed leaf. b: Specimen U 1049, lobe detail showing finely serrate leaf margin. c: Specimen T 0246, 9-lobed leaf with coarsely serrate leaf margin. d: Oriolo MSF 645-1, 9-lobed leaf with two small additional lobes. e: Oriolo MSF 645. f: Oriolo MSF 660, 9-lobed specimen. g: Oriolo MSF 660-1. White arrows indicate position along lamina lobes where marginal serration starts. Scale bars 10 mm (a–c, f, g), 50 mm (d, e).
Text-fig. 4. Charred grass from diatomite of Saint-Bauzile. a: Overview of diatomite slab with one larger specimen of charred grass (left) and several smaller, lath-shaped charcoal fragments; SM.B 22260; scale bar = 1 cm. b: Detail of vein exhibited on split grass blade, with stomata oriented parallel to vein. c: Stomata oriented in rows and bands parallel to veins exposed on split grass blade. d: Surface of grass leaf with rectangular, elongated cells with strongly undulating margins in an intercostal area. in Evidence For Wildfires During Deposition Of The Late Miocene Diatomites Of The Konservat-Lagerstätte Lake Saint-Bauzile (Ardèche, France) - Preliminary Results
Text-fig. 4. Charred grass from diatomite of Saint-Bauzile. a: Overview of diatomite slab with one larger specimen of charred grass (left) and several smaller, lath-shaped charcoal fragments; SM.B 22260; scale bar = 1 cm. b: Detail of vein exhibited on split grass blade, with stomata oriented parallel to vein. c: Stomata oriented in rows and bands parallel to veins exposed on split grass blade. d: Surface of grass leaf with rectangular, elongated cells with strongly undulating margins in an intercostal area.
Text-fig. 2. Nymphaea sp. from the Miocene Clarkia Lake flora, Locality P-33. a: Photograph of the fossil leaf. b: Sketch of leaf showing the salient features of shape, basal lobes and margin, eccentric insertion point of the abaxial petiole, and primary actinodromous venation. Dashed lines represent torn edge of lamina; dotted line is outline of right basal lobe. Line drawing by P. Martin Sander. Scale bar applies to both photo and drawing. in First Water Lily, A Leaf Of Nymphaea Sp., From The Miocene Clarkia Flora, Northern Idaho, Usa: Occurrence, Taphonomic Observations, Floristic Implications
Text-fig. 2. Nymphaea sp. from the Miocene Clarkia Lake flora, Locality P-33. a: Photograph of the fossil leaf. b: Sketch of leaf showing the salient features of shape, basal lobes and margin, eccentric insertion point of the abaxial petiole, and primary actinodromous venation. Dashed lines represent torn edge of lamina; dotted line is outline of right basal lobe. Line drawing by P. Martin Sander. Scale bar applies to both photo and drawing.
Text-fig. 1. Context and location of the Govone outcrop. a: Location of the Piedmont Basin at the northern margin of the Mediterranean Basin and distribution of Messinian evaporites. b: Simplified geological map of the Piedmont Basin showing the location of the Govone outcrop close to the town of Alba. in Remains Of A Subtropical Humid Forest In A Messinian Evaporitebearing Succession At Govone, Northwestern Italy - Preliminary Results
Text-fig. 1. Context and location of the Govone outcrop. a: Location of the Piedmont Basin at the northern margin of the Mediterranean Basin and distribution of Messinian evaporites. b: Simplified geological map of the Piedmont Basin showing the location of the Govone outcrop close to the town of Alba.
Text-fig. A3. a: Leaf morphotype 1 Tebano MSF SG 049. b: Leaf morphotype 2 Oriolo MSF 631. c: Leaf morphotype 3 Oriolo MSF n.n. d, f: Leaf morphotype 4. d: Oriolo MSF 891. e: Oriolo MSF 856. f: Oriolo MSF 858. g: Leaf morphotype 5 Oriolo MSF 783. h: Leaf morphotype 6 Oriolo MSF 952. i: Leaf morphotype 7 Oriolo MSF 862. j, l: Leaf morphotype 8. j: Oriolo MSF 912. k: Oriolo MSF 662. l: Oriolo MSF 662-1. m: Leaf morphotype 9 Oriolo MSF 715. n: Leaf morphotype 10 Oriolo MSF 716. o: Leaf morphotype 11, overview and detail of margin Oriolo MSF 880. p–z: Various rosaceous leaves/ leaflets. p: Oriolo MSF 943. q: Oriolo MSF 890. r: Oriolo MSF 950. s: Oriolo MSF 958. t: Oriolo MSF 966 aff. Sorbus. u: Oriolo MSF 956. v: Oriolo MSF 961. w: Oriolo MSF 962. x: Oriolo MSF 874. y: Oriolo MSF 883. z: Oriolo MSF 960. in The Late Early Pleistocene Flora Of Oriolo, Faenza (Italy): Assembly Of The Modern Forest Biome
Text-fig. A3. a: Leaf morphotype 1 Tebano MSF SG 049. b: Leaf morphotype 2 Oriolo MSF 631. c: Leaf morphotype 3 Oriolo MSF n.n. d, f: Leaf morphotype 4. d: Oriolo MSF 891. e: Oriolo MSF 856. f: Oriolo MSF 858. g: Leaf morphotype 5 Oriolo MSF 783. h: Leaf morphotype 6 Oriolo MSF 952. i: Leaf morphotype 7 Oriolo MSF 862. j, l: Leaf morphotype 8. j: Oriolo MSF 912. k: Oriolo MSF 662. l: Oriolo MSF 662-1. m: Leaf morphotype 9 Oriolo MSF 715. n: Leaf morphotype 10 Oriolo MSF 716. o: Leaf morphotype 11, overview and detail of margin Oriolo MSF 880. p–z: Various rosaceous leaves/ leaflets. p: Oriolo MSF 943. q: Oriolo MSF 890. r: Oriolo MSF 950. s: Oriolo MSF 958. t: Oriolo MSF 966 aff. Sorbus. u: Oriolo MSF 956. v: Oriolo MSF 961. w: Oriolo MSF 962. x: Oriolo MSF 874. y: Oriolo MSF 883. z: Oriolo MSF 960.
Text-fig. 11. a: Sapindopsis sp., 3rd Kamenka, Frentsevka Formation, early-middle Albian, spec. IBSS 40-1; b, c: Trochodendroides sp., Konstantinovka, Galenki Formation, early-middle Albian, spec. IBBS 11/145, b – upper part of leaf, c – crenate margin; d: Dicotylophyllum sp. 2, Konstantinovka, Galenki Formation, early-middle Albian, spec. IBBS 11/133; e: Sapindopsis cf. angusta (HEER) SEWARD et V.M.CONWAY, Andreev Inlet, Frentsevka Formation, early-middle Albian, spec. IBSS 28/104; f: Sapindopsis variabilis FONTAINE, Bikin River, Alchan Formation, early-middle Albian, spec. IBSS 4561/124-1; g: Laurophyllum sp., Konstantinovka, Galenki Formation, early-middle Albian, spec. IBBS 11/131. Scale bar 1 cm in a, b, d, f, g and 5 mm in c, e. in Angiosperm Diversification In The Early Cretaceous Of Primorye, Far East Of Russia
Text-fig. 11. a: Sapindopsis sp., 3rd Kamenka, Frentsevka Formation, early-middle Albian, spec. IBSS 40-1; b, c: Trochodendroides sp., Konstantinovka, Galenki Formation, early-middle Albian, spec. IBBS 11/145, b – upper part of leaf, c – crenate margin; d: Dicotylophyllum sp. 2, Konstantinovka, Galenki Formation, early-middle Albian, spec. IBBS 11/133; e: Sapindopsis cf. angusta (HEER) SEWARD et V.M.CONWAY, Andreev Inlet, Frentsevka Formation, early-middle Albian, spec. IBSS 28/104; f: Sapindopsis variabilis FONTAINE, Bikin River, Alchan Formation, early-middle Albian, spec. IBSS 4561/124-1; g: Laurophyllum sp., Konstantinovka, Galenki Formation, early-middle Albian, spec. IBBS 11/131. Scale bar 1 cm in a, b, d, f, g and 5 mm in c, e.
Pest defenses under weak selection exert a limited influence on the evolution of height growth and drought avoidance in marginal pine populations
<p>Whilst droughts, intensified by climate change, have been affecting forests worldwide, pest epidemics are a major source of uncertainty for assessing drought impacts on forest trees. Thus far, little information has documented the adaptability and evolvability of traits related to drought and pests simultaneously. We conducted common-garden experiments to investigate how several phenotypic traits (i.e., height growth, drought avoidance based on water-use efficiency inferred from δ<sup>13</sup>C, and pest resistance based on defense traits) interact in five mature lodgepole pine populations established in four progeny trials in western Canada. The relevance of interpopulation variation in climate sensitivity highlighted that seed-source warm populations had greater adaptive capability than cold populations. In test sites, warming generated taller trees with higher δ<sup>13</sup>C and increased the evolutionary potential of height growth and δ<sup>13</sup>C across populations. We found, however, no pronounced gradient in defenses and their evolutionary potential along populations or test sites. Response to selection was weak in defenses across test sites, but high for height growth, particularly at warm test sites. Response to selection of δ<sup>13</sup>C varied depending on its selective strength relative to height growth. We conclude that warming could promote the adaptability and evolvability of growth response and drought avoidance with limited evolutionary influence from pest (biotic) pressures.</p>
Text-fig. 9. Carpolithes (a–r). a–d: Carpolithes sp. 5. USNM PAL 772370. Scale bar = 5 mm, reflected light, palladium coated. a: Lateral view of seed, apex up, possible raphe descending from apex toward viewer. b: Lateral view of seed, apex up, possible raphe on right. c: Lateral view, opposite side, apex up, possible raphe on left. d: Apical view, note central pit with raphe descending towards bottom margin. e–h: Carpolithes sp. 6. USNM PAL 772371. Scale bar = 5 mm. e: Basal view illustrating depression and keel in plane of bisymmetry, reflected light, palladium coated. f–h: Micro-CT scan surface rendering. f: Lateral view showing relatively smooth rounded surface. g: Specimen rotated 180° from (f), surface partially eroded. h: Longitudinal view, showing median keel. i–m: Carpolithes sp. 7 USNM PAL 772372. Scale bar = 5 mm. i: View of intact face of globose fruit, possible apical constriction at top. j: Lateral view, intact surface to right, possible apical constriction at top, both micro-CT scan surface renderings. k: Apical view. l: Face view illustrating the mineral filling and the fine, radiating structure of the fruit wall on the left and right margins, both reflected light, palladium coated. m: Closeup of the cellular layer on the left of (l), micro-CT scan surface rendering. n–p: Carpolithes sp. 8. USNM PAL 772373. Scale bar = 3 mm, reflected light, palladium coated. n: Lateral view of pyrene-like structure, one ridge running vertically in the center of view, the other two forming the left and right margins. o: Lateral view of pyrene-like structure, ridge in (n) on the left. p: End-on view illustrating one convex, one concave, and one relatively flat to very slightly concave face. q, r: Carpolithes sp. 9 USNM PAL 772374. Scale bar = 5 mm, reflected light, palladium coated. q: Exterior of the smooth broken half-sphere. r: Interior of the broken half-sphere. in The Early Middle Eocene Wagon Bed Carpoflora Of Central Wyoming, U.S.A.
Text-fig. 9. Carpolithes (a–r). a–d: Carpolithes sp. 5. USNM PAL 772370. Scale bar = 5 mm, reflected light, palladium coated. a: Lateral view of seed, apex up, possible raphe descending from apex toward viewer. b: Lateral view of seed, apex up, possible raphe on right. c: Lateral view, opposite side, apex up, possible raphe on left. d: Apical view, note central pit with raphe descending towards bottom margin. e–h: Carpolithes sp. 6. USNM PAL 772371. Scale bar = 5 mm. e: Basal view illustrating depression and keel in plane of bisymmetry, reflected light, palladium coated. f–h: Micro-CT scan surface rendering. f: Lateral view showing relatively smooth rounded surface. g: Specimen rotated 180° from (f), surface partially eroded. h: Longitudinal view, showing median keel. i–m: Carpolithes sp. 7 USNM PAL 772372. Scale bar = 5 mm. i: View of intact face of globose fruit, possible apical constriction at top. j: Lateral view, intact surface to right, possible apical constriction at top, both micro-CT scan surface renderings. k: Apical view. l: Face view illustrating the mineral filling and the fine, radiating structure of the fruit wall on the left and right margins, both reflected light, palladium coated. m: Closeup of the cellular layer on the left of (l), micro-CT scan surface rendering. n–p: Carpolithes sp. 8. USNM PAL 772373. Scale bar = 3 mm, reflected light, palladium coated. n: Lateral view of pyrene-like structure, one ridge running vertically in the center of view, the other two forming the left and right margins. o: Lateral view of pyrene-like structure, ridge in (n) on the left. p: End-on view illustrating one convex, one concave, and one relatively flat to very slightly concave face. q, r: Carpolithes sp. 9 USNM PAL 772374. Scale bar = 5 mm, reflected light, palladium coated. q: Exterior of the smooth broken half-sphere. r: Interior of the broken half-sphere.
Text-fig. 10. a–d: Araliaephyllum luciferum (KRYSHT.) GOLOVN., Partizansk, Severosuchan Formation, Aptian, a – spec. TSNIGRM 3013/1, lectotype, b – spec TSNIGRM 3013/2, c – spec. TSNIGRM 3013/4, d – spec. TSNIGRM 3013/3; e, j: Pandanites ahnertii (KRYSHT.) GOLOVN., Konstantinovka, Lipovtsy Formation, Aptian, TSNIGRM 3013/5, e – fragment of leaf margin, j – general view, j1 – lectotype, j2 – leaf, figured in (e); f: Araliaephyllum ussuriense (KRASSILOV) GOLOVN., Andreev Inlet, Frentsevka Formation, early-middle Albian, spec. IBBS 28/103; g: Araliaephyllum vittenburgii GOLOVN. et VOLYNETS, Podgorodenka coalfield, Galenki Formation, early-middle Albian, spec. IBBS 41/1, g1 – spec. IBBS 41/1a, holotype, g2 – spec. IBBS 41/1b; h: Dicotylophyllum sp. 1, Podgorodenka coalfield, Lipovtsy Formation, Aptian, spec. IBBS 28L-4; i: Sapindopsis sp., 3rd Kamenka, Frentsevka Formation, early-middle Albian, spec. IBSS 325/8. Scale bar 5 mm in a–h and 1 cm in i, j. in Angiosperm Diversification In The Early Cretaceous Of Primorye, Far East Of Russia
Text-fig. 10. a–d: Araliaephyllum luciferum (KRYSHT.) GOLOVN., Partizansk, Severosuchan Formation, Aptian, a – spec. TSNIGRM 3013/1, lectotype, b – spec TSNIGRM 3013/2, c – spec. TSNIGRM 3013/4, d – spec. TSNIGRM 3013/3; e, j: Pandanites ahnertii (KRYSHT.) GOLOVN., Konstantinovka, Lipovtsy Formation, Aptian, TSNIGRM 3013/5, e – fragment of leaf margin, j – general view, j1 – lectotype, j2 – leaf, figured in (e); f: Araliaephyllum ussuriense (KRASSILOV) GOLOVN., Andreev Inlet, Frentsevka Formation, early-middle Albian, spec. IBBS 28/103; g: Araliaephyllum vittenburgii GOLOVN. et VOLYNETS, Podgorodenka coalfield, Galenki Formation, early-middle Albian, spec. IBBS 41/1, g1 – spec. IBBS 41/1a, holotype, g2 – spec. IBBS 41/1b; h: Dicotylophyllum sp. 1, Podgorodenka coalfield, Lipovtsy Formation, Aptian, spec. IBBS 28L-4; i: Sapindopsis sp., 3rd Kamenka, Frentsevka Formation, early-middle Albian, spec. IBSS 325/8. Scale bar 5 mm in a–h and 1 cm in i, j.
Fig. 1. – Flower structure. A. Scrophularia sulaimanica S.A in Taxonomic revision of the broad-margined calyx species of Scrophularia (Scrophulariaceae) in Iran, with one new species
Fig. 1. – Flower structure. A. Scrophularia sulaimanica S.A. Ahmad; B. Scrophularia haematantha Boiss. & Heldr.; C. Scrophularia kollakii S.A. Ahmad; D. Scrophularia mesopotamica Boiss.; E. Scrophularia pruinosa Boiss.; F. Scrophularia rosulata Stiefelh.; G. Scrophularia sanguinea Grau; H. Scrophularia sardashtensis Ranjbar & Rahch.; I. Scrophularia valida Grau.
Fig. 5 in Taxonomic revision of the broad-margined calyx species of Scrophularia (Scrophulariaceae) in Iran, with one new species
Fig. 5. – Holotype of Scrophularia sardashtensis Ranjbar & Rahch. A. Habit; B. Upper cauline leaf (abaxial surface); C. Upper cauline leaf (adaxial surface).
Fig. 3 in Taxonomic revision of the broad-margined calyx species of Scrophularia (Scrophulariaceae) in Iran, with one new species
Fig. 3. – Distribution map of the broad-margined calyx species of Scrophularia L. in Iran. Scrophularia haematantha Boiss. & Heldr. (white squares), S. kollakii S.A. Ahmad (black stars), S. mesopotamica Boiss. (black triangles), S. pruinosa Boiss. (black squares), S. rosulata Stiefelh. (black circles), S. sanguinea Grau (white circles), S. sardashtensis Ranjbar & Rahch. (black diamonds), S. sulaimanica S.A. Ahmad (white stars), and S. valida Grau (white triangles).
ScienceDex guides
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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.