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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).
Text-fig. 47. Scanning electron microscope (SEM) images of reticulate-foveolate pollen on the surface of a fruit of Serialis antiquum; Torres Vedras locality, Portugal. a, b) Pollen grain showing angular outline and tectum perforated by foveolae of different sizes; note the braided tectum ornamentation formed by aggregations of small ridges (b); aperture not known; c, d) Pollen grain showing angular outline, tectum perforated by foveolae that become smaller toward the presumed pole; note the relatively smooth tectum and faint pattern of braiding ridges (d); aperture not known. Specimens, TV43-S171535-01 (a, b), TV43-S171535-02 (c, d). Scale bars 6 Μm (a, c), 1 Μm (b, 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. 47. Scanning electron microscope (SEM) images of reticulate-foveolate pollen on the surface of a fruit of Serialis antiquum; Torres Vedras locality, Portugal. a, b) Pollen grain showing angular outline and tectum perforated by foveolae of different sizes; note the braided tectum ornamentation formed by aggregations of small ridges (b); aperture not known; c, d) Pollen grain showing angular outline, tectum perforated by foveolae that become smaller toward the presumed pole; note the relatively smooth tectum and faint pattern of braiding ridges (d); aperture not known. Specimens, TV43-S171535-01 (a, b), TV43-S171535-02 (c, d). Scale bars 6 Μm (a, c), 1 Μm (b, d).
Text-fig. 45. Scanning electron microscope (SEM) images of monocolpate pollen of Dinisia portugallica gen. et sp. nov. from a fragmentary stamen; Torres Vedras locality, Portugal. a) Holotype; stamen fragment showing elongated pollen sacs that yielded the pollen in this Text-figure; b) Two pollen grains showing poorly defined distal aperture (arrowhead) and distinctive vermiform reticulum forming luminae of variable shapes and sizes; note especially the irregularly and incomplete reticulum in the grain on the left; c) Reticulum showing smooth, vermiform muri attached to the smooth surface of the foot layer by long columellae; note that columellae often terminate segments of muri that are not closed; d, e) Pollen grains showing proximal surface (d), poorly defined distal aperture (e, arrowhead) and distinctive vermiform reticulum supported by long columellae; note dense covering of small, spherical orbicules on the inner surface of the anther wall. Specimen, TV44-S148216 (holotype). Scale bars 300 Μm (a), 6 Μm (b, d, e), 3 Μm (c). 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. 45. Scanning electron microscope (SEM) images of monocolpate pollen of Dinisia portugallica gen. et sp. nov. from a fragmentary stamen; Torres Vedras locality, Portugal. a) Holotype; stamen fragment showing elongated pollen sacs that yielded the pollen in this Text-figure; b) Two pollen grains showing poorly defined distal aperture (arrowhead) and distinctive vermiform reticulum forming luminae of variable shapes and sizes; note especially the irregularly and incomplete reticulum in the grain on the left; c) Reticulum showing smooth, vermiform muri attached to the smooth surface of the foot layer by long columellae; note that columellae often terminate segments of muri that are not closed; d, e) Pollen grains showing proximal surface (d), poorly defined distal aperture (e, arrowhead) and distinctive vermiform reticulum supported by long columellae; note dense covering of small, spherical orbicules on the inner surface of the anther wall. Specimen, TV44-S148216 (holotype). Scale bars 300 Μm (a), 6 Μm (b, d, e), 3 Μm (c).
Text-fig. 4. Scanning electron microscope (SEM) images of megaspores with possible affinities to Selaginellales; Torres Vedras locality, Portugal. a, b) Hughesisporites galericulatus, lateral view of megaspore (a) with almost smooth surface and spore wall of thin elements forming a dense reticulum (b); c) Trileites sp., proximal view of megaspore with almost smooth surface and raised trilete mark; d–f) Rugotriletes sp., proximal (e) and lateral (f) views of megaspores showing coarsely reticulate-rugulate surface ornamentation and prominent gula around the trilete mark and compact perforate spore wall (d); g, h) Erlansonisporites sp., distal (g) and lateral (h) views of megaspores showing coarsely reticulate-rugulate surface and fibrous spore wall; i, j) Striatriletes sp. 1, megaspore in oblique proximal view (i) showing raised laesurae and irregular striate-rugulate surface, and detail of spore wall (j) showing dense packing of sculptural elements; k, l) Striatriletes sp. 2, megaspore in proximal view (k) showing trilete mark, striate-rugulate surface, and detail of spore wall (l) composed of loosely packed fibers; m) Striatriletes sp. 3, megaspore in proximal view showing raised trilete mark and striate-rugulate surface; n, o) Verrutriletes sp., megaspore in oblique proximal view (n) showing short laesurae of the trilete mark, and the dense verrucate surface (o); p) Megaspore sp. 1, oblique proximal view showing 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. 4. Scanning electron microscope (SEM) images of megaspores with possible affinities to Selaginellales; Torres Vedras locality, Portugal. a, b) Hughesisporites galericulatus, lateral view of megaspore (a) with almost smooth surface and spore wall of thin elements forming a dense reticulum (b); c) Trileites sp., proximal view of megaspore with almost smooth surface and raised trilete mark; d–f) Rugotriletes sp., proximal (e) and lateral (f) views of megaspores showing coarsely reticulate-rugulate surface ornamentation and prominent gula around the trilete mark and compact perforate spore wall (d); g, h) Erlansonisporites sp., distal (g) and lateral (h) views of megaspores showing coarsely reticulate-rugulate surface and fibrous spore wall; i, j) Striatriletes sp. 1, megaspore in oblique proximal view (i) showing raised laesurae and irregular striate-rugulate surface, and detail of spore wall (j) showing dense packing of sculptural elements; k, l) Striatriletes sp. 2, megaspore in proximal view (k) showing trilete mark, striate-rugulate surface, and detail of spore wall (l) composed of loosely packed fibers; m) Striatriletes sp. 3, megaspore in proximal view showing raised trilete mark and striate-rugulate surface; n, o) Verrutriletes sp., megaspore in oblique proximal view (n) showing short laesurae of the trilete mark, and the dense verrucate surface (o); p) Megaspore sp. 1, oblique proximal view showing
Text-fig. 18. Scanning electron microscope (SEM) images of a fruit of Canrightia sp. with associated pollen; Torres Vedras locality, Portugal. a) Fruit in lateral view showing prominent cavities in the fruit wall formed by the scattered oil bodies and the broad hypanthium fused to the base of the fruit (arrowhead); b) Fruit surface showing epidermal cells and the scattered oil cells embedded in the fruit wall (arrowheads); c) Cluster of monocolpate pollen grains in the probable stigmatic region of the fruit; d) Pollen grains showing the long colpus and semitectate-reticulate pollen wall; e) Pollen wall showing the reticulum with large and small lumina, and scattered, compressed columellae supporting the smooth muri. Specimen, TV142-S170213. Scale bars 300 Μm (a), 100 Μm (b), 30 Μm (c), 6 Μm (d), 1 Μm (e). 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. 18. Scanning electron microscope (SEM) images of a fruit of Canrightia sp. with associated pollen; Torres Vedras locality, Portugal. a) Fruit in lateral view showing prominent cavities in the fruit wall formed by the scattered oil bodies and the broad hypanthium fused to the base of the fruit (arrowhead); b) Fruit surface showing epidermal cells and the scattered oil cells embedded in the fruit wall (arrowheads); c) Cluster of monocolpate pollen grains in the probable stigmatic region of the fruit; d) Pollen grains showing the long colpus and semitectate-reticulate pollen wall; e) Pollen wall showing the reticulum with large and small lumina, and scattered, compressed columellae supporting the smooth muri. Specimen, TV142-S170213. Scale bars 300 Μm (a), 100 Μm (b), 30 Μm (c), 6 Μm (d), 1 Μm (e).
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).
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)
Text-fig. 11. Scanning electron microscope (SEM) images of seeds assigned to the BEG group (a–d) and associated pollen grains (e–i); Torres Vedras locality, Portugal. a) Seed of Tomcatia taylorii showing the four horns formed by extensions of the envelope and the central projection of the envelope that surrounds to the micropylar tube; b, c) Seeds of Quadrispermum parvum in lateral (b) and apical (c) views showing the transverse ribs and the central projection of the envelope that surrounds the micropylar tube; d–f) Seeds of Ephedrispermum lusitanicum showing the four-angled seed envelope (d), the micropylar tube surrounded by the tissues of the integument (e), and ephedroid pollen grains on the seed surface (f); g) Apex of seed of Quadrispermum parvum showing simple 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. 11. Scanning electron microscope (SEM) images of seeds assigned to the BEG group (a–d) and associated pollen grains (e–i); Torres Vedras locality, Portugal. a) Seed of Tomcatia taylorii showing the four horns formed by extensions of the envelope and the central projection of the envelope that surrounds to the micropylar tube; b, c) Seeds of Quadrispermum parvum in lateral (b) and apical (c) views showing the transverse ribs and the central projection of the envelope that surrounds the micropylar tube; d–f) Seeds of Ephedrispermum lusitanicum showing the four-angled seed envelope (d), the micropylar tube surrounded by the tissues of the integument (e), and ephedroid pollen grains on the seed surface (f); g) Apex of seed of Quadrispermum parvum showing simple
Text-fig. 3. Stratigraphic section through part of the Ashawq Formation at the Omanitherium type locality, Dhofar Governorate, Oman. Beds A–D are indurated cliff-forming strata identified in the accompanying field photographs (Textfigs 4, 5). Note the increase in marine influence as one ascends through the section, the fauna in Beds A and B being dominated by freshwater molluscs and land snails, with few brackish water specimens, whereas the biota in Bed D is frankly marine with a single specimen of the freshwater snail Pila. Bed C yielded Vermetus, oysters and sponges, but also contains abundant land snails and a low diversity of freshwater gastropods. in Large Mammals From The Rupelian Of Oman - Recent Finds
Text-fig. 3. Stratigraphic section through part of the Ashawq Formation at the Omanitherium type locality, Dhofar Governorate, Oman. Beds A–D are indurated cliff-forming strata identified in the accompanying field photographs (Textfigs 4, 5). Note the increase in marine influence as one ascends through the section, the fauna in Beds A and B being dominated by freshwater molluscs and land snails, with few brackish water specimens, whereas the biota in Bed D is frankly marine with a single specimen of the freshwater snail Pila. Bed C yielded Vermetus, oysters and sponges, but also contains abundant land snails and a low diversity of freshwater gastropods.
Figure 7. Two Cambrian trilobites. A–D in Hybridization in the evolution of animal form and life-cycle
Figure 7. Two Cambrian trilobites. A–D, stages in the development of Sao hirsute: A, protaspis; B–D, early segmented stages. E, adult Agnostus pisiformis. Scale bar = ∼1 mm (A–D from Borradaile et al., 1935; E redrawn after Fortey, 2000.)
Figure 5. Ophiolimna bairdi postlarval development. A–D, 1 in Who's who among baby brittle stars (Echinodermata: Ophiuroidea): postmetamorphic development of some North Atlantic forms
Figure 5. Ophiolimna bairdi postlarval development. A–D, 1 mm dd postlarvae; A, dorsal; B, arm dorsal; C, arm ventral; D, ventral; E, 1.6 mm dd postlarva dorsal; F, 1.6 mm dd ventral; G, same, jaw; H, 2 mm dd postlarva. Abbreviations: BS, buccal scale; MP, mouth papilla; OP, oral plate; others as in Figs 1, 2. Scale bars in millimetres.
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).
Text-fig. 2. Scanning electron microscope (SEM, a, c–f) and synchrotron radiation X-ray tomographic microscopy (SRXTM, b, g) images of the flower of Mugideiriflora portugallica (a, b) and fruits, seeds and pollen of Canrightia resinifera (c–g); Catefica locality, Portugal. a) Oblique, apical view of flower showing multiparted organization with numerous laminar tepals, stamens that are rhomboidal and flattened in transverse section and carpels that are borne on the short conical apex of the receptacle; b) Transverse section (orthoslice xy0800) through basal part of flower showing the elongate bases of the laminar tepals and the flattened rhomboidal bases of the stamens; c) Fruit in lateral view showing irregular surface resulting from the abundant resin bodies in the fruit and hypanthium wall, scars from stamens on the rim of the hypanthium (arrowheads) and the lobed apical stigmatic region (st); d) Broken fruit with one or two seeds missing but showing three pendant, orthotropous seeds with pointed micropylar regions (mi) and a finely pitted crystalliferous endotesta; note the remains of the apical vascular bundles (vb); e) Single seed isolated from a fruit showing two distinct bundles (vb) still attached apically to the chalazal region of the seed, the pointed micropyle (mi) and the finely pitted surface of the crystalliferous endotesta; f) Monocolpate pollen from stigmatic region of fruit showing the long colpus and coarse reticulum; g) Transverse section (orthoslice xy0705) through a fruit showing four seeds all with radially elongated endothelium cells formed from the inner epidermis of the tegmen (asterisks). Specimens, Catefica 150-S174254 (a, b), Catefica 49-S170377 (c), Catefica 49-S170372 (d), Catefica 50-S170401 (e), Catefica 50-S170404 (f), Catefica 50-S174906 (g). Scale bars = 300 Μm (a–e, g), 6 Μm (f). in The Early Cretaceous Mesofossil Flora Of Catefica, Portugal: Angiosperms
Text-fig. 2. Scanning electron microscope (SEM, a, c–f) and synchrotron radiation X-ray tomographic microscopy (SRXTM, b, g) images of the flower of Mugideiriflora portugallica (a, b) and fruits, seeds and pollen of Canrightia resinifera (c–g); Catefica locality, Portugal. a) Oblique, apical view of flower showing multiparted organization with numerous laminar tepals, stamens that are rhomboidal and flattened in transverse section and carpels that are borne on the short conical apex of the receptacle; b) Transverse section (orthoslice xy0800) through basal part of flower showing the elongate bases of the laminar tepals and the flattened rhomboidal bases of the stamens; c) Fruit in lateral view showing irregular surface resulting from the abundant resin bodies in the fruit and hypanthium wall, scars from stamens on the rim of the hypanthium (arrowheads) and the lobed apical stigmatic region (st); d) Broken fruit with one or two seeds missing but showing three pendant, orthotropous seeds with pointed micropylar regions (mi) and a finely pitted crystalliferous endotesta; note the remains of the apical vascular bundles (vb); e) Single seed isolated from a fruit showing two distinct bundles (vb) still attached apically to the chalazal region of the seed, the pointed micropyle (mi) and the finely pitted surface of the crystalliferous endotesta; f) Monocolpate pollen from stigmatic region of fruit showing the long colpus and coarse reticulum; g) Transverse section (orthoslice xy0705) through a fruit showing four seeds all with radially elongated endothelium cells formed from the inner epidermis of the tegmen (asterisks). Specimens, Catefica 150-S174254 (a, b), Catefica 49-S170377 (c), Catefica 49-S170372 (d), Catefica 50-S170401 (e), Catefica 50-S170404 (f), Catefica 50-S174906 (g). Scale bars = 300 Μm (a–e, g), 6 Μm (f).
Data platform (genotyping data set) related to ERDF postdoctoral project No. 1.1.1.2/VIAA/4/20/718 "The role of vitamin D gene polymorphisms and its receptors in the modulation of intestinal inflammation in patients with relapsing and progressive forms of multiple sclerosis".
<p><strong>Data platform </strong><strong>(genotyping dataset)</strong> <strong>related to the ERDF postdoctoral project No. </strong><strong>1.1.1.2/VIAA/4/20/718</strong><strong> “</strong><strong>The role of vitamin D and its receptor gene polymorphisms in the modulation of intestinal inflammation in patients with relapsing and progressive forms of multiple sclerosis</strong><strong>”.</strong></p> <p><strong>About the project and gathered data:</strong></p> <p>The dataset contains genotyping data on 289 sex-balanced samples (approximately 60% women / 40% men)) were created at the the multiple sclerosis (MS) Clinic of the Latvian Maritime Medical Center (LMMC) in 2011 (disease duration of 1-51 years); the collection was updated within the framework of the ERDF MS project (2017-2020) and replenished during the ERDF postdoctoral project No. 1.1.1.2/VIAA/4/20/718 “The role of vitamin D and its receptor gene polymorphisms in the modulation of intestinal inflammation in patients with relapsing and progressive forms of multiple sclerosis” (2021-2023).</p> <p>For the <strong>Genotyping dataset </strong>relevant information for each patient from the MS disease cohort, referring to proteasomal gene genetic variations (microsatellites and SNPs): (HSMS006 <em>(PSMA6),</em> HSMS602 <em>(FAM177A1),</em> HSMS701 <em>(KIAA0391)</em>, HSMS702 <em>(KIAA0391)</em> HSMS801 <em>(KIAA0391)</em>, rs11543947<em>(PSMB5), </em>rs2277460 (mi110), rs1048990 (mi8)<em> (PSMA6),</em> rs1048990 (mi8)<em> (PSMA6),</em> rs2295826/rs2295827<em>(PSMC6),</em> rs2348071 <em>(PSMA3),</em> rs2071543, rs9357155 <em>(PSMB8),</em> rs17587<em>(PSMB9),</em> rs74421874 <em>(PSMD9); </em>rs9275596 from HLA region; vitamin D-related genes (VDR and GC) polymorphisms: rs2228570, rs1544410, rs7975232, rs731236 (<em>VDR</em>) and rs7041, rs4588 <em>(GC).</em></p>
Global Star-formation Properties Extracted from Synthetic Star-forming Regions | Appendix D
<p>We provide in this online-material measured dust surface density maps, dust temperature maps and corresponding <span class="math-tex">\(\chi^2\)</span> maps of a synthetic star-forming region described in detail in Chapter 5 of the PhD thesis.</p> <p>Please cite the following papers:</p> <p>http://adsabs.harvard.edu/abs/2017ApJ...849….3K<br> http://adsabs.harvard.edu/abs/2017ApJS..233....1K<br> http://adsabs.harvard.edu/abs/2017ApJ...849….1K</p>
FIGURE 17. Eriophyes tiliae Nalepa 1890. Deutogyne female. D in Eriophyes species (Acari: Eriophyoidea) inhabiting lime trees (Tilia spp.: Tiliaceae) — supplementary description and morphological variability related to host plants and female forms
FIGURE 17. Eriophyes tiliae Nalepa 1890. Deutogyne female. D. Dorsal view; SA. Lateral view of anterior region; CG. Coxigenital region; IG. Internal genitalia; L1. Leg I; L2. Leg II. em. Empodium (enlarged). Scale bar: 50 µm for D, CG, IG & SA; 25 µm for L1 & L2.
FIGURE 15. Eriophyes tiliae Nalepa 1890. Protogyne female. D in Eriophyes species (Acari: Eriophyoidea) inhabiting lime trees (Tilia spp.: Tiliaceae) — supplementary description and morphological variability related to host plants and female forms
FIGURE 15. Eriophyes tiliae Nalepa 1890. Protogyne female. D. Dorsal view; SA. Lateral view of anterior region; CG. Coxigenital region; IG. Internal genitalia; L1. Leg I; L2. Leg II. em. Empodium (enlarged). Male. E. Epiandrium. Scale bar: 50 µm for D, SA, CG, E & IG; 25 µm for L1 & L2.
FIGURE 1. A–D in A new Neotibicen cicada subspecies (Hemiptera: Cicadidae) from the southeastern USA forms hybrid zones with a widespread relative despite a divergent male calling song
FIGURE 1. A–D, Neotibicen similaris apalachicola, n. subsp., dorsal view, ventral view, pygofer ventral view, pygofer lateral view (holotype specimen 08.US.FL.TRA.03). E–H, N. similaris similaris, dorsal view, ventral view, pygofer ventral view, pygofer lateral view (specimen 08.US.GA.HAH.01). Scale bars = 12.5 mm.
Figure 2. Ascothoracida. A–D in The evolutionary diversity of barnacles, with an updated classification of fossil and living forms
Figure 2. Ascothoracida. A–D, larval diversity of selected Ascothoracida. A, an early, live Baccalaureus nauplius larva. B, an early, live Zibrowia nauplius larva. C, D, a Tessmann's larva or a-cypris (C), with hooked antennules (D). E–N, adult diversity of selected Ascothoracida. E–G, the coral Turbinaria, showing the galls formed by the ascothoracidan Petrarca. Insert in E shows the galls in cross-section, with red Petrarca inside the coral skeleton. F, Petrarca. G, magnified view of Petrarca. H, Synagoga arabesque, with extended, hooked first antennules. I, J, Ascothorax rybakovi on the brittle star Ophiacantha pacifica. K, a free Dengrogaster sp. L–N, the zoanthid Palythoa with Baccalaureus sp. inside. Abbreviation: a1, first antennule. Fig 2C photographed by ND and Dr. Jørgen Olesen, Natural History Museum of Denmark.
Subspecies and Distribution. M. d. decemlineata Grandidier, 1867 — CW Madagascar (Menabe region). M. d. lineata Pocock, 1915 — SW Madagascar (S of the Mangoky River). The previous records ofthis form in the Lac Tsimanampetsotsa area are misidentified specimens of Grandidier's Vontsira. in Eupleridae
Subspecies and Distribution. M. d. decemlineata Grandidier, 1867 — CW Madagascar (Menabe region). M. d. lineata Pocock, 1915 — SW Madagascar (S of the Mangoky River). The previous records ofthis form in the Lac Tsimanampetsotsa area are misidentified specimens of Grandidier's Vontsira.
ScienceDex guides
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Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.