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zenodo40/100

Text-fig. 7. Scanning electron micrographs (a, b, d, e, g–k), X-ray microtomographic orthoslices (c) and synchrotron radiation X-ray tomographic microscopy orthoslices (f) of fruits and endocarps of uncertain affinity from Zliv-Řídká Blana locality. a–c: Trebecenia sarcocalis, a – tricarpellate fruit, no. NM-F 3637, b – fruits supported by pentamerous and persistent calyx, no. NMF 3637, c – fruit almost circular in transverse section, no. NM-F 3637; d: Taxon 17, small fruit with slightly sunken stylar region, no. NM-F 3201; e: Taxon 19, spherical fruit, the fruit wall composed of large isodiametric, thick walled cells, no. NM-F 3181; f: Taxon 19, single-seeded fruit, no. NM-F 3621; g: Taxon 20, syncarpous, multicarpellate fruit of ten carpels, no. NM-F 3200; h: Taxon 22, syncarpous, multicarpellate fruit of seven carpels, no. NM-F 3159; i: cf. Sabia menispermoides, endocarp of drupaceous fruits, no. NM-F 4624; j: Taxon 25, endocarp triangular in cross-section, no. NM-F 3218; k: Taxon 24, endocarp spherical in cross-section with a distinctly ribbed and foveolate surface, no. NM-F 3217. in Plant Mesofossils From The Late Cretaceous Klikov Formation, The Czech Republic

Text-fig. 7. Scanning electron micrographs (a, b, d, e, g–k), X-ray microtomographic orthoslices (c) and synchrotron radiation X-ray tomographic microscopy orthoslices (f) of fruits and endocarps of uncertain affinity from Zliv-Řídká Blana locality. a–c: Trebecenia sarcocalis, a – tricarpellate fruit, no. NM-F 3637, b – fruits supported by pentamerous and persistent calyx, no. NMF 3637, c – fruit almost circular in transverse section, no. NM-F 3637; d: Taxon 17, small fruit with slightly sunken stylar region, no. NM-F 3201; e: Taxon 19, spherical fruit, the fruit wall composed of large isodiametric, thick walled cells, no. NM-F 3181; f: Taxon 19, single-seeded fruit, no. NM-F 3621; g: Taxon 20, syncarpous, multicarpellate fruit of ten carpels, no. NM-F 3200; h: Taxon 22, syncarpous, multicarpellate fruit of seven carpels, no. NM-F 3159; i: cf. Sabia menispermoides, endocarp of drupaceous fruits, no. NM-F 4624; j: Taxon 25, endocarp triangular in cross-section, no. NM-F 3218; k: Taxon 24, endocarp spherical in cross-section with a distinctly ribbed and foveolate surface, no. NM-F 3217.

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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

opencc-by-4.0Feb 2022View details →
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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 &lt;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.

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Text-fig. 3. Cercidiphyllum cf. alalongum R.A.SCOTT et E.A.WHEELER, UF 279-24543. a, b: Diffuse-porous wood, exclusively solitary vessels, axial parenchyma rare, thick-walled fibers, TS. c: Scalariform perforation plate with more than 30 bars, RLS. d: Helical thickenings (HT) in vessel element tip, RLS. e: Opposite to scalariform intervessel pits, RLS. f, g: Heterocellular rays 1–2 cells wide, occasionally uniseriate and biseriate portions of similar width, TLS. h: Ray with alternating rows of procumbent and upright (-square) cells, RLS. Scale bars: 200 µm in a; 100 µm in b, f; 50 µm in c, g, h; 20 µm in d, e. in A Diverse Assemblage Of Late Eocene Woods From Oregon, Western Usa

Text-fig. 3. Cercidiphyllum cf. alalongum R.A.SCOTT et E.A.WHEELER, UF 279-24543. a, b: Diffuse-porous wood, exclusively solitary vessels, axial parenchyma rare, thick-walled fibers, TS. c: Scalariform perforation plate with more than 30 bars, RLS. d: Helical thickenings (HT) in vessel element tip, RLS. e: Opposite to scalariform intervessel pits, RLS. f, g: Heterocellular rays 1–2 cells wide, occasionally uniseriate and biseriate portions of similar width, TLS. h: Ray with alternating rows of procumbent and upright (-square) cells, RLS. Scale bars: 200 µm in a; 100 µm in b, f; 50 µm in c, g, h; 20 µm in d, e.

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Text-fig. 5. SRXTM images of Miranthus elegans gen. et sp. nov.; Mira locality, Portugal. a, b: Transverse sections of flower (a, orthoslice xy0665 close to the apex of placenta; b, orthoslice xy0800 in middle part of placenta) showing remains of calyx with distinct bundles (arrows), ovary wall (ow) and numerous ovules (ov) on the central mushroom-shaped globose placenta (pl) with central column (cc). c: Transverse section of flower (orthoslice xy0620) through perianth and ovary (ow) at a level above the placenta showing ovules (ov) and cellular preservation of the sepal bundles (arrows shown for one sepal); note abaxial surface of sepals with thick-walled epidermal cells, thick cuticle, and fine pointed verrucae. d: Longitudinal section of flower (orthoslice xz0500) showing perigynous position of calyx and semi-inferior ovary (ow, ovary wall) with a central placenta (pl), central column (cc) and numerous ovules (ov); note spiny verrucae on abaxial surface of calyx lobes. Specimens, Mira 100-S153145 (a, b), Mira 100-S170155 (c, d, holotype). Scale bars = 600 µm (a–d). in Early Flowers Of Primuloid Ericales From The Late Cretaceous Of Portugal And Their Ecological And Phytogeographic Implications

Text-fig. 5. SRXTM images of Miranthus elegans gen. et sp. nov.; Mira locality, Portugal. a, b: Transverse sections of flower (a, orthoslice xy0665 close to the apex of placenta; b, orthoslice xy0800 in middle part of placenta) showing remains of calyx with distinct bundles (arrows), ovary wall (ow) and numerous ovules (ov) on the central mushroom-shaped globose placenta (pl) with central column (cc). c: Transverse section of flower (orthoslice xy0620) through perianth and ovary (ow) at a level above the placenta showing ovules (ov) and cellular preservation of the sepal bundles (arrows shown for one sepal); note abaxial surface of sepals with thick-walled epidermal cells, thick cuticle, and fine pointed verrucae. d: Longitudinal section of flower (orthoslice xz0500) showing perigynous position of calyx and semi-inferior ovary (ow, ovary wall) with a central placenta (pl), central column (cc) and numerous ovules (ov); note spiny verrucae on abaxial surface of calyx lobes. Specimens, Mira 100-S153145 (a, b), Mira 100-S170155 (c, d, holotype). Scale bars = 600 µm (a–d).

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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.

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Text-fig. 6. Transmitted light microphotographs of permineralized wood from Govone. a, b: cf. Cupressinoxylon sp., radial section, MGPT-PU141105, a – nodular end of ray parenchyma (arrow), b – thick and pitted horizontal walls of ray parenchyma (arrow). c–f: Pinaceae gen. et sp. indet., MGPT-PU141107, c – abnormal discoloration due to ecological disruptions (radial section), d – rays up to 10 cells high, uniseriate, partly biseriate (black arrow), intercellular spaces observed (white arrows) (tangential section), e – large, thick-walled axial resin canal with more than 9 epithelial cells observed, axial resin canal diameter>60 Μm (transverse section), f – spiral thickenings due to compression (white arrow) (radial section). in Remains Of A Subtropical Humid Forest In A Messinian Evaporitebearing Succession At Govone, Northwestern Italy - Preliminary Results

Text-fig. 6. Transmitted light microphotographs of permineralized wood from Govone. a, b: cf. Cupressinoxylon sp., radial section, MGPT-PU141105, a – nodular end of ray parenchyma (arrow), b – thick and pitted horizontal walls of ray parenchyma (arrow). c–f: Pinaceae gen. et sp. indet., MGPT-PU141107, c – abnormal discoloration due to ecological disruptions (radial section), d – rays up to 10 cells high, uniseriate, partly biseriate (black arrow), intercellular spaces observed (white arrows) (tangential section), e – large, thick-walled axial resin canal with more than 9 epithelial cells observed, axial resin canal diameter&gt;60 Μm (transverse section), f – spiral thickenings due to compression (white arrow) (radial section).

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Text-fig. 50. Scanning electron microscope (SEM, a, b) and synchrotron radiation X-ray tomographic microscopy (SRXTM, c–f) images of "Foveolate seed sp. 2"; Catefica locality, Portugal. a, b) Lateral (a) and apical (b) views of seed showing the coarsely foveolate surface; note the truncate apex and the slightly depressed hilar-micropylar region; c) Longitudinal section (volume rendering cut between orthoslices xz0740 and xz0840) through the middle of seed showing the truncate apex with slightly depressed hilar-micropylar region and basal rounded chalazal region; note thick outer integument (oi) composed of an exotesta of thickwalled palisade-like cells and a thin inner integument (ii); d, e, f) Transverse (d, orthoslice xy0800) and longitudinal sections (e, orthoslice xz1100, f, orthoslice yz0800) through seed hilar-micropylar region, showing the exotesta comprised of the thick-walled palisade-like cells of the outer integument (oi), small, thin-walled meso- endotestal cells of the outer integument (arrows) and thin inner integument (ii). Specimen, Catefica 153-S172332 (a–f). Scale bars = 300 Μm (a–f). in The Early Cretaceous Mesofossil Flora Of Catefica, Portugal: Angiosperms

Text-fig. 50. Scanning electron microscope (SEM, a, b) and synchrotron radiation X-ray tomographic microscopy (SRXTM, c–f) images of "Foveolate seed sp. 2"; Catefica locality, Portugal. a, b) Lateral (a) and apical (b) views of seed showing the coarsely foveolate surface; note the truncate apex and the slightly depressed hilar-micropylar region; c) Longitudinal section (volume rendering cut between orthoslices xz0740 and xz0840) through the middle of seed showing the truncate apex with slightly depressed hilar-micropylar region and basal rounded chalazal region; note thick outer integument (oi) composed of an exotesta of thickwalled palisade-like cells and a thin inner integument (ii); d, e, f) Transverse (d, orthoslice xy0800) and longitudinal sections (e, orthoslice xz1100, f, orthoslice yz0800) through seed hilar-micropylar region, showing the exotesta comprised of the thick-walled palisade-like cells of the outer integument (oi), small, thin-walled meso- endotestal cells of the outer integument (arrows) and thin inner integument (ii). Specimen, Catefica 153-S172332 (a–f). Scale bars = 300 Μm (a–f).

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Text-fig. 49. Scanning electron microscope (SEM, a, b) and synchrotron radiation X-ray tomographic microscopy (SRXTM, c–e) images of "Foveolate seed sp. 1"; Catefica locality, Portugal. a) Lateral view of seed showing foveolate surface; note the slightly pointed hilar-micropylar region with the preservation of a presumed secretion (arrow) from the micropyle; b) Detail of seed surface showing shallow pitting and very faint outlines of the undulate anticlinal walls of the exotestal cells; c) Longitudinal section (volume rendering cut between orthoslices yz0450 and yz0460) through the middle of the seed showing the slightly pointed hilarmicropylar region and the rounded chalazal region; note the thick exotesta of the outer integument composed of thick-walled palisade-like cells (oi); note partial preservation of large cells of the nutritive tissue (nu) and the smaller cells of the embryo (em) at the micropylar end of the seed; d, e) Longitudinal sections (d, orthoslice xz0750, e, orthoslice yz0485) through middle of the seed perpendicular to each other showing the hilar-micropylar region with the preservation of a presumed secretion from micropyle (e, arrow), thick palisade-like cells of outer integument (oi), larger cells of the nutritive tissue (nu) and remains of the smaller cells of the embryo (em). Specimen, Catefica 49-S172316 (a–e). Scale bars = 300 Μm (a, c–e), 50 Μm (b). in The Early Cretaceous Mesofossil Flora Of Catefica, Portugal: Angiosperms

Text-fig. 49. Scanning electron microscope (SEM, a, b) and synchrotron radiation X-ray tomographic microscopy (SRXTM, c–e) images of "Foveolate seed sp. 1"; Catefica locality, Portugal. a) Lateral view of seed showing foveolate surface; note the slightly pointed hilar-micropylar region with the preservation of a presumed secretion (arrow) from the micropyle; b) Detail of seed surface showing shallow pitting and very faint outlines of the undulate anticlinal walls of the exotestal cells; c) Longitudinal section (volume rendering cut between orthoslices yz0450 and yz0460) through the middle of the seed showing the slightly pointed hilarmicropylar region and the rounded chalazal region; note the thick exotesta of the outer integument composed of thick-walled palisade-like cells (oi); note partial preservation of large cells of the nutritive tissue (nu) and the smaller cells of the embryo (em) at the micropylar end of the seed; d, e) Longitudinal sections (d, orthoslice xz0750, e, orthoslice yz0485) through middle of the seed perpendicular to each other showing the hilar-micropylar region with the preservation of a presumed secretion from micropyle (e, arrow), thick palisade-like cells of outer integument (oi), larger cells of the nutritive tissue (nu) and remains of the smaller cells of the embryo (em). Specimen, Catefica 49-S172316 (a–e). Scale bars = 300 Μm (a, c–e), 50 Μm (b).

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Text-fig. 47. Synchrotron radiation X-ray tomographic microscopy (SRXTM) images of "One-seeded fruit sp. 1"; Catefica locality, Portugal. a, b) Lateral view of fruits showing slightly sinuous ventral margin and the curved stalk; c, d) Longitudinal sections perpendicular to each other through the median part of fruit and its single seed (c, orthoslice yz0652, d, xz0739) showing the bitegmic seed closely adhering to the fruit wall (fw); the several cell layer thick outer integument (oi) and the membranous inner integument (ii); note the vascular bundle (vb) branching into a dorsal and lateral bundle near the base of the fruit; e) Transverse section (orthoslice xy0600) showing fruit wall (fw) and outer (oi) and inner (ii) integuments of the seed; f) Longitudinal section (orthoslice yz0871) through the micropylar region showing micropyle (mi) formed from membranous inner integument (ii). Specimens, Catefica 49-S174927 (a), Catefica 49-S174923 (b, f), Catefica 49-S174769 (c–e). Scale bars = 300 Μm (a–d), 100 Μm (e, f). in The Early Cretaceous Mesofossil Flora Of Catefica, Portugal: Angiosperms

Text-fig. 47. Synchrotron radiation X-ray tomographic microscopy (SRXTM) images of "One-seeded fruit sp. 1"; Catefica locality, Portugal. a, b) Lateral view of fruits showing slightly sinuous ventral margin and the curved stalk; c, d) Longitudinal sections perpendicular to each other through the median part of fruit and its single seed (c, orthoslice yz0652, d, xz0739) showing the bitegmic seed closely adhering to the fruit wall (fw); the several cell layer thick outer integument (oi) and the membranous inner integument (ii); note the vascular bundle (vb) branching into a dorsal and lateral bundle near the base of the fruit; e) Transverse section (orthoslice xy0600) showing fruit wall (fw) and outer (oi) and inner (ii) integuments of the seed; f) Longitudinal section (orthoslice yz0871) through the micropylar region showing micropyle (mi) formed from membranous inner integument (ii). Specimens, Catefica 49-S174927 (a), Catefica 49-S174923 (b, f), Catefica 49-S174769 (c–e). Scale bars = 300 Μm (a–d), 100 Μm (e, f).

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Text-fig. 3. Synchrotron radiation X-ray tomographic microscopy (SRXTM) images of fruits of Canrightia foveolata sp. nov.; Catefica locality, Portugal. a) Volume rendering of fruit showing prominent rim around the middle of the fruit with reduced tepals (arrowheads) and partly abraded fruit wall exposing the pitted endotesta surface of one of two seeds (arrow); note two of the vascular bundles (vb) extending from the base of the fruit to the tepals; b) Voltex of fruit showing prominent rim around the fruit (arrowhead) and dense precipitation of crystals in the endothelium cells of one of the two seeds in the fruit; c) Longitudinal section of fruit (orthoslice yz0520) showing the inferred hypanthium rim (arrow head) and two seeds, one with a dense precipitation of crystals; note the prominent endothelium cells (asterisks) of the inner integument and the well-developed fruit wall above the seeds; d) Transverse section through basal part of fruit and seeds close to the micropyle (orthoslice xy0312) showing partly abraded fruit wall with five vascular bundles (vb) and details of the seed coat with endotesta (oi-end) surrounding the tegmen consisting of an outer epidermis (ii-o), middle layer (ii-m) and a distinct inner epidermis (endothelium) consisting of radially elongated cells (asterisk); e) Transverse section (orthoslice xy1680) through apical part of the fruit close to chalaza showing the tips of two seeds; note the endotesta (oi-end) surrounded by thick-walled cells of the exotesta (oi-o); f) Transverse section (orthoslice xy1485) through fruit in the region of the hypanthium rim showing sections through the two seeds close to the chalazal region; note endotesta (oi-end) surrounded by larger cells of exotesta (oi-o) and fruit wall (fr). Specimen, Catefica 49-S174249 (holotype, a–f). Scale bars = 300 Μm (a–c, e, f), 100 Μm (d). in The Early Cretaceous Mesofossil Flora Of Catefica, Portugal: Angiosperms

Text-fig. 3. Synchrotron radiation X-ray tomographic microscopy (SRXTM) images of fruits of Canrightia foveolata sp. nov.; Catefica locality, Portugal. a) Volume rendering of fruit showing prominent rim around the middle of the fruit with reduced tepals (arrowheads) and partly abraded fruit wall exposing the pitted endotesta surface of one of two seeds (arrow); note two of the vascular bundles (vb) extending from the base of the fruit to the tepals; b) Voltex of fruit showing prominent rim around the fruit (arrowhead) and dense precipitation of crystals in the endothelium cells of one of the two seeds in the fruit; c) Longitudinal section of fruit (orthoslice yz0520) showing the inferred hypanthium rim (arrow head) and two seeds, one with a dense precipitation of crystals; note the prominent endothelium cells (asterisks) of the inner integument and the well-developed fruit wall above the seeds; d) Transverse section through basal part of fruit and seeds close to the micropyle (orthoslice xy0312) showing partly abraded fruit wall with five vascular bundles (vb) and details of the seed coat with endotesta (oi-end) surrounding the tegmen consisting of an outer epidermis (ii-o), middle layer (ii-m) and a distinct inner epidermis (endothelium) consisting of radially elongated cells (asterisk); e) Transverse section (orthoslice xy1680) through apical part of the fruit close to chalaza showing the tips of two seeds; note the endotesta (oi-end) surrounded by thick-walled cells of the exotesta (oi-o); f) Transverse section (orthoslice xy1485) through fruit in the region of the hypanthium rim showing sections through the two seeds close to the chalazal region; note endotesta (oi-end) surrounded by larger cells of exotesta (oi-o) and fruit wall (fr). Specimen, Catefica 49-S174249 (holotype, a–f). Scale bars = 300 Μm (a–c, e, f), 100 Μm (d).

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Cell wall thickness and composition are involved in photosynthetic limitation

<p><span><span><span><span><span><span><span><span><span><span><span>The key role of cell walls in setting mesophyll conductance to CO<sub>2</sub> (<i>g</i><sub>m</sub>) and, consequently, photosynthesis, is reviewed. First, the theoretical properties of cell walls that can affect <i>g</i><sub>m</sub> are presented. Then, we focus on cell wall thickness (<i>T</i><sub>cw</sub>) reviewing empirical evidence showing that <i>T</i><sub>cw</sub> varies strongly among species and phylogenetic groups in a way that correlates with <i>g</i><sub>m</sub> and photosynthesis i.e. the thicker the mesophyll cell walls, the lower <i>g</i><sub>m</sub> and photosynthesis. Potential interplays of <i>g</i><sub>m</sub>, <i>T</i><sub>cw</sub>, dehydration tolerance and hydraulic properties of leaves are also discussed. Dynamic variations of <i>T</i><sub>cw</sub> in response to the environment and their implications in the regulation of photosynthesis are discussed, and recent evidence suggesting an influence of cell wall composition on <i>g</i><sub>m</sub> are presented. We then propose a hypothetical mechanism for the influence of cell walls on photosynthesis, combining the effects of thickness and composition, particularly pectins. Finally, we discuss the prospects for using biotechnology for enhancing photosynthesis by means of altering cell wall-related genes.</span></span></span></span></span></span></span></span></span></span></span></p>

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Cell wall thickness and composition are involved in photosynthetic limitation

Open the record for dataset details and reuse information.

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zenodo28/100

Text-fig. 4. Synchrotron radiation X-ray tomographic microscopy (SRXTM) images of seeds of Canrightia foveolata sp. nov.; Catefica locality, Portugal. a–d) Volume renderings of abraded seeds in ventral (a), lateral (b, d) and apical (c) views showing the slightly protruding chalaza (arrows) and dense longitudinal grooves with shallow pits in the surface of the endotesta; e) Transverse section of seed (orthoslice xy0665) showing the irregular grooved surface of the endotesta (oi-en) and the tegmen comprised of two layers of thick-walled cells that surround the cells of the prominent endothelium (asterisk); f) Longitudinal section (orthoslice xz1195) through seed showing the thin-walled endothelium cells (asterisk) surrounded by the thicker cells of the outer tegmen and endotesta; g) Longitudinal section (orthoslice yz0727) through seed showing outlines of angular crystals evenly distributed in cells of the endotesta (oi-en); note the outer epidermis of the tegmen (ii-o) composed of thick-walled cells; h) Longitudinal section (orthoslice xz0940) of seed showing details of the chalazal region with course of the vascular bundle (vb), cells of the prominent endothelium (asterisk), crystalliferous endotesta of the outer integument (oi-en) and the distinct thick walled cells of the outer cells of the tegmen (ii-o); i) Longitudinal and tangential section (orthoslice yz0542) through the endotesta (oi-en) showing the outlines of densely spaced crystals. Specimens, Catefica 242-S175178 (a–c, e–h), Catefica 49-S175179 (d, i). Scale bars = 300 Μm (a–d), 100 Μm (e, f, h, i), 50 Μm (g). in The Early Cretaceous Mesofossil Flora Of Catefica, Portugal: Angiosperms

Text-fig. 4. Synchrotron radiation X-ray tomographic microscopy (SRXTM) images of seeds of Canrightia foveolata sp. nov.; Catefica locality, Portugal. a–d) Volume renderings of abraded seeds in ventral (a), lateral (b, d) and apical (c) views showing the slightly protruding chalaza (arrows) and dense longitudinal grooves with shallow pits in the surface of the endotesta; e) Transverse section of seed (orthoslice xy0665) showing the irregular grooved surface of the endotesta (oi-en) and the tegmen comprised of two layers of thick-walled cells that surround the cells of the prominent endothelium (asterisk); f) Longitudinal section (orthoslice xz1195) through seed showing the thin-walled endothelium cells (asterisk) surrounded by the thicker cells of the outer tegmen and endotesta; g) Longitudinal section (orthoslice yz0727) through seed showing outlines of angular crystals evenly distributed in cells of the endotesta (oi-en); note the outer epidermis of the tegmen (ii-o) composed of thick-walled cells; h) Longitudinal section (orthoslice xz0940) of seed showing details of the chalazal region with course of the vascular bundle (vb), cells of the prominent endothelium (asterisk), crystalliferous endotesta of the outer integument (oi-en) and the distinct thick walled cells of the outer cells of the tegmen (ii-o); i) Longitudinal and tangential section (orthoslice yz0542) through the endotesta (oi-en) showing the outlines of densely spaced crystals. Specimens, Catefica 242-S175178 (a–c, e–h), Catefica 49-S175179 (d, i). Scale bars = 300 Μm (a–d), 100 Μm (e, f, h, i), 50 Μm (g).

opencc-by-4.0Dec 2022View details →
zenodo28/100

Text-fig. 23. Synchrotron radiation X-ray tomographic microscopy (SRXTM) images of Ibericarpus cuneiformis gen. et sp. nov.; Catefica locality, Portugal. a) Longitudinal section (orthoslice yz0827) showing fruitlet with apical stigmatic region and a single seed enclosed within the fruitlet wall that has a thick epidermal cuticle; note the tiny embryo (emb) internal to the micropyle (mi) and oriented toward the base of the fruitlet; b) Transverse section through apical part of two fruitlets (orthoslice xy0810) showing the fruitlet wall (fr) composed of small thin-walled cells covered by an epidermis of isodiametric cells (ep) with a thick outer cuticle (cu); c) Longitudinal section (orthoslice xz0370) through basal part of fruitlet perpendicular to section in (a) showing the micropyle (mi), embryo (emb) composed of tiny cells, and the thick cuticle (cu) covering the bulging cells of the fruitlet epidermis. Specimen, Catefica 50-S174907 (a–c). Scale bars = 300 Μm (a–c). in The Early Cretaceous Mesofossil Flora Of Catefica, Portugal: Angiosperms

Text-fig. 23. Synchrotron radiation X-ray tomographic microscopy (SRXTM) images of Ibericarpus cuneiformis gen. et sp. nov.; Catefica locality, Portugal. a) Longitudinal section (orthoslice yz0827) showing fruitlet with apical stigmatic region and a single seed enclosed within the fruitlet wall that has a thick epidermal cuticle; note the tiny embryo (emb) internal to the micropyle (mi) and oriented toward the base of the fruitlet; b) Transverse section through apical part of two fruitlets (orthoslice xy0810) showing the fruitlet wall (fr) composed of small thin-walled cells covered by an epidermis of isodiametric cells (ep) with a thick outer cuticle (cu); c) Longitudinal section (orthoslice xz0370) through basal part of fruitlet perpendicular to section in (a) showing the micropyle (mi), embryo (emb) composed of tiny cells, and the thick cuticle (cu) covering the bulging cells of the fruitlet epidermis. Specimen, Catefica 50-S174907 (a–c). Scale bars = 300 Μm (a–c).

opencc-by-4.0Dec 2022View details →

ScienceDex guides

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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.

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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