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Fig. 5 in Variation in the colour and shape of capitula in Parkia bicolor (Leguminosae) illustrated by two watercolours from southern Nigeria painted by Dorothy Amaury Talbot (1871-1916)
Fig. 5. – Watercolour of Parkia bicolor A. Chev. by Dorothy Amaury Talbot, mounted upside down, the capitulum on the left
Fig. 2. – Parkia bicolor A. Chev. A in Variation in the colour and shape of capitula in Parkia bicolor (Leguminosae) illustrated by two watercolours from southern Nigeria painted by Dorothy Amaury Talbot (1871-1916)
Fig. 2. – Parkia bicolor A. Chev. A. Capitulum approaching anthesis, Korup National Park, Cameroon; B. Capitulum at anthesis, Bouvala, Ngounié Prov., Gabon. Images not to scale.
Fig. 1 in Variation in the colour and shape of capitula in Parkia bicolor (Leguminosae) illustrated by two watercolours from southern Nigeria painted by Dorothy Amaury Talbot (1871-1916)
Fig. 1. – The principal localities where the Talbots collected specimens of Parkia bicolor A. Chev. in south-eastern Nigeria, and Korup National Park, Cameroon, where Regine Grünmeier studied pollination and floral biology. [QGIS, http://www.qgis.org]
Fig. 5. Nematostylis incarnata Kainul. A in A taxonomic revision of the Malagasy endemic genus Nematostylis (Rubiaceae), with description of two new species
Fig. 5. Nematostylis incarnata Kainul. A. Treelet growing in thicket; B. Flowering branch (note the flush of new leaves with persistent older leaves); C. Bottom-view of an inflorescence, showing leafy bracts; D. Side-view of an inflorescence; E. Infructescence with acropetally maturing fruits (note the now translucent calycophylls); F. Top-view of an inflorescence (note the bright yellow disks of the flowers).
Fig. 3 in A taxonomic revision of the Malagasy endemic genus Nematostylis (Rubiaceae), with description of two new species
Fig. 3. Nematostylis anthophylla (A. Rich. ex DC.) Baill. A. Flower buds; B, C. Habitat and habit; D, E. Flowering branches; F. Young fruits.
Fig. 1 in A taxonomic revision of the Malagasy endemic genus Nematostylis (Rubiaceae), with description of two new species
Fig. 1. Distribution map of Nematostylis anthophylla (A. Rich. ex DC.) Baill. (circles), N. citriflora Kainul. (squares), and N. incarnata Kainul. (triangles) in Madagascar mapped on the bioclimatic zones
Fig. 4. Nematostylis citriflora Kainul. A, B in A taxonomic revision of the Malagasy endemic genus Nematostylis (Rubiaceae), with description of two new species
Fig. 4. Nematostylis citriflora Kainul. A, B. Habit and habitat; C. Leaves; D–G. Flowering branches; H. Young fruits.
Figs 7–12 in Two New Species Of Macrorrhyncha Winnertz (Diptera: Keroplatidae) From Turkey, With Redescription Of Macrorrhyncha Thracica Bechev, Stat. N. And A Key To The Western Palaearctic Species Of The Genus
Figs 7–12. Male terminalia, setae are shown on gonostyles only: 7 = Macrorrhyncha thracica, form of tergite 9 and cerci, dorsal view; 8 = M. thracica, ventral view; 9 = M. thracica – lateral view; 10 = M. geranias, dorsal view; 11 = M. geranias, ventral view; 12 = M. geranias, lateral view
Figs 1–6 in Two New Species Of Macrorrhyncha Winnertz (Diptera: Keroplatidae) From Turkey, With Redescription Of Macrorrhyncha Thracica Bechev, Stat. N. And A Key To The Western Palaearctic Species Of The Genus
Figs 1–6. Male terminalia, setae are shown on gonostyles only: 1 = Macrorrhyncha anatolica, form of tergite 9 and cerci, dorsal view; 2 = M. anatolica, ventral view; 3 = M. anatolica, lateral view; 4 = M. muglensis, form of tergite 9 and cerci, dorsal view; 5 = M. muglensis, ventral view; 6 = M. muglensis, lateral view. Abbreviations: lf = lateral fold of tergite 9, ip = inner process of gonocoxite,
Fig. 8 a-i in Palaeoxylotomical Studies In The Cenozoic Petrified Forests Of Greece. Part Two - Conifers
Fig. 8 a-i, (graphic scale). Glyptostroboxylon tenerum (Kraus) Conwentz, 1884; (Specimen Li.483). a-c: Cross section - quite abrupt transition, distinct growth rings; large thin-walled tracheids; parenchyma few, diffuse; d-f: Tangential section - irregular uniseriate small pits on tracheids; parenchima with nodular end walls (arrow); rays exclusively uniseriate; g-i: Radial section - tracheidal pitting 1-2-seriate, opposite; rays homocellular, cells all procumbent; cross field with 1-2(-3) cupressoid pits or taxodioid (arrows), more numerous in marginal cross fields, and slightly irregular.
Fig. 6 a-i in Palaeoxylotomical Studies In The Cenozoic Petrified Forests Of Greece. Part Two - Conifers
Fig. 6 a-i, (graphic scale). Taxodioxylon taxodii Gothan, 1906. (Specimen Tf.122). a-c: Cross section - quite gradual transition, distinct growth rings; large tracheids; parenchyma few, diffuse; d-f: Tangential section - pitting on tracheids absent; axial parenchyma end-walls nodular (arrow); rays uniseriate; g-i: Radial section - tracheidal pitting 1-2-seriate, pairs opposite; rays homocellular, cells all procumbent; poorly preserved cross field pitting with 1-2(4) taxodioid oculipores.
Fig. 7 a-i in Palaeoxylotomical Studies In The Cenozoic Petrified Forests Of Greece. Part Two - Conifers
Fig. 7 a-i (graphic scale). Glyptostroboxylon rudolphii Dolezych et van der Burgh, 2004; (Specimen Li.481) a-c: Cross section - abrupt transition, quite distinct growth rings; thick-walled tracheids; d-f: Tangential section - few pits on tracheids, parenchyma with nodular transverse wall; rays exclusively uniseriate; g-i:. Radial section - radial pitting 1-3- seriate, opposite; rays homogeneous, parenchymal cells sll procumbent, marginals taller; poorly preserved cross-fields with 1-4 glyptostroboid to taxodioid pits (arrows).
Fig. 4 a-i in Palaeoxylotomical Studies In The Cenozoic Petrified Forests Of Greece. Part Two - Conifers
Fig. 4 a-i. (graphic scale). Tetraclinoxylon velitzelosii Süss, 1997. (Specimen Tf.132). a-c: Cross section - quite abrupt transition, distinct growth rings; tracheids with typicaly round lumina (arrow); parenchyma few; d-f: Tangential section - pitting on tracheids absent; parenchyma with dark remains; low rays (arrow); g-i: Radial section - stiations on tracheids (arrow) and pitting 1(2)-seriate, opposite or irregular; poorly preserved cross fields (arrow).
Fig. 2 a-i in Palaeoxylotomical Studies In The Cenozoic Petrified Forests Of Greece. Part Two - Conifers
Fig. 2 a-i, (graphic scale). Cupressinoxylon akdikii Özgüven-Ertan, 1977 (Specimen Lfk.156). a–c: Cross section - abrupt transition, distinct growth rings; parenchyma few, diffuse; rays uniseriate; d–f: Tangential section - pitting on tracheids absent or rare, as uniseriate small pits (arrow); rays uniseriate; g–i: Radial section - tracheidal pitting 1(-2)- seriate, opposite; rays homogeneous, badly preserved cross fields with 1-2(-3) cupressoid pits (arrow).
Fig. 3 a-i in Palaeoxylotomical Studies In The Cenozoic Petrified Forests Of Greece. Part Two - Conifers
Fig. 3 a-i. (graphic scale). Juniperoxylon acarcae Akkemik, 2020. (Specimen Lfk.266). a–c: Cross section - transition abrupt, distinct growth rings; parenchyma few, diffuse; rays uniseriate; d–f: Tangential section - pitting on tracheids absent; nodular parenchyma end walls (arrow); rays uniseriate; g–i: Radial section - tracheidal pitting uniseriate; rays homocellular, cells all procumbent, marginals taller; tangential end-walls with juniperoid nodules (inclined arrow); poorly preserved cross fields with 1-2 cupressoid pits, usually arranged as vertical pairs pits (horizontal arrow).
Fig. 1 in Palaeoxylotomical Studies In The Cenozoic Petrified Forests Of Greece. Part Two - Conifers
Fig. 1 Map of Greece; * marks the areas where the studied fossil wood samples were collected (according with d-maps.com, with modifications).
Fig. 5 a-i in Palaeoxylotomical Studies In The Cenozoic Petrified Forests Of Greece. Part Two - Conifers
Fig. 5 a-i, (graphic scale). Taxodioxylon gypsaceum (Göpp.) Kräusel, 1949. (Specimen Lfk.313). a-c: Cross section - quite gradual transition, distinct growth rings; parenchyma few, diffuse, or in small lines; d-f: Tangential section - unpitted tracheids; parenchyma with end-wall smooth or weakly nodular; g–i: Radial section - tracheidal pitting 1-3-seriate, opposite; rays homocellular, cells all procumbent; poorly preserved cross fields with 1-3 taxodioid pits (arrow), more numerous in taller marginal cross fields, in 2 superposed rows or slightly irregular.
Fig. 9 a-i in Palaeoxylotomical Studies In The Cenozoic Petrified Forests Of Greece. Part Two - Conifers
Fig. 9 a-i. (graphic scale). Pinuxylon pineoides (Kraus) Koeniguer, 1967; (Specimen Lsv.365). a-c: Cross section - gradual transition, distinct growth rings; parenchyma absent; resin canals of pinoid type, with thin walledepithelial cells, partially destroyed; d-f: Tangential section - tracheids, uniseriate rays, axial canal (4), fusiform ray with ray-canal (5-6); g-i: Radial section - tracheidal pitting 1-2-seriate, opposite (8); rays homocellular, cells all procumbent, ray-tracheids weakly dentate; poorly preserved cross-field with 1-3(4) pinoid pits.
Fig. 2 3D in Probable Juvenile Frontal Of Daspletosaurus Horneri (Dinosauria: Theropoda) From The Two Medicine Formation Of Montana, With Implications For Tyrannosaurid Ontogeny
Fig. 2 3D model of UCM 55499, left frontal of a juvenile cf. Daspletosaurus horneri, in A, dorsal view; B, ventral view; C, rostral view; D, lateral view; E, medial view; F, caudal view. Abbreviations: cbf, cerebral fossa; ccr, crista cranii; cpos, caudal part of postorbital suture; cr, cylinder-like ridge; cs, caudal shelf; dtf, dorsotemporal fossa; dtr, dorsotemporal ridge; es, ethmoid scar; fh, forehead region; ifs, interfrontal suture; lac, lacrimal socket; lss, laterosphenoid suture; ms, joint surface for the mesethmoid; obf, olfactory bulb fossa; or, orbital wall; os, orbital slot; oss, orbitosphenoid suture; pb, postorbital buttress; prf, joint surface for prefrontal; ps, parietal suture; rpos, rostral part of postorbital suture; sc, sagittal crest. The model is courtesy of The Fossil Vertebrate Collection at the University of Colorado Boulder Museum of Natural History.
Fig. 1 UCM 55499 in Probable Juvenile Frontal Of Daspletosaurus Horneri (Dinosauria: Theropoda) From The Two Medicine Formation Of Montana, With Implications For Tyrannosaurid Ontogeny
Fig. 1 UCM 55499, left frontal of a juvenile cf. Daspletosaurus horneri, in A, dorsal view; B, ventral view; C, rostral view; D, lateral view; E, medial view; F, caudal view. Abbreviations: cbf, cerebral fossa; ccr, crista cranii; cpos, caudal part of postorbital suture; cr, cylinder-like ridge; cs, caudal shelf; dtf, dorsotemporal fossa; dtr, dorsotemporal ridge; es, ethmoid scar; fh, forehead region; ifs, interfrontal suture; lac, lacrimal socket; lss, laterosphenoid suture; ms, joint surface for the mesethmoid; obf, olfactory bulb fossa; or, orbital wall; os, orbital slot; oss, orbitosphenoid suture; pb, postorbital buttress; prf, joint surface for prefrontal; ps, parietal suture; rpos, rostral part of postorbital suture; sc, sagittal crest. Images are courtesy of The Fossil Vertebrate Collection at the University of Colorado Boulder Museum of Natural History. vidual variation. Furthermore, the area between the postsurface of TMP 2013.018.0011 (14.2°; Voris et al., 2019: orbital buttress and the caudal shelf in UCM 55499 is fig. 2) and that of the postorbital suture and the ros- extremely thin and plate-like, similar to the condition trocaudal axis (19.7°) in the lateral surface of UCM reported in the holotype of tyrannosaurine Alioramus 55499 are comparable to each other. Additionally, the "altai" (Bever et al., 2013) but differs from the relatively laterosphenoid suture in UCM 55499 is facing caudoven- deep condition in juvenile Gorgosaurus (e.g., Voris et al., trally, unlike the subvertical, caudally-facing suture in 2019: fig. S15). Lastly, Gorgosaurus does not approach Gorgosaurus frontals (e.g., Yun, 2020; pers. obs). This the abundance of Daspletosaurus horneri in the Two appears to be consistent with the description of Voris Medicine Formation (e.g., Farlow & Pianka, 2002; Carr (2018), who noted the angle between frontal and later- et al., 2017; Voris et al., 2020). In summary, the combiosphenoid sutures in Daspletosaurus postorbitals is ob- nation of aforementioned Daspletosaurus-like or tyrantuse, in which the former slopes caudoventrally. Further- nosaurine-like features, differences from similarly-sized more, the mediolateral width of the caudal shelf in UCM Gorgosaurus frontals as well as its provenance favours 55499 is slightly wider than that of the postorbital but- identification of the specimen as Daspletosaurus horneri tress, which is reminiscent to the condition in tyranno- through a balance of probability. saurines (Voris, 2018; Voris et al., 2022). In contrast, the widest part of the albertosaurine frontals is located at the Comparative description: UCM 55499 is an isolated, rostral end of postorbital suture (Voris, 2018; Voris et al., mostly complete left frontal that lacks the nasal process, 2022). Thus, UCM 55499 can be identified as a tyranno- the rostral part of the area that articulated with the presaurine, of which Daspletosaurus horneri is the only frontal, and the dorsal part of the sagittal crest. As preknown example in the Two Medicine Formation. There- served, the maximum rostrocaudal length of the specimen fore, this specimen is probably referable to this taxon. is 82 mm. When measured after the methodology of Cur- Of note, UCM 55499 does resemble Gorgosaurus front- rie (2003a), the width and depth are 44 mm and 18 mm, als by possessing mediolaterally oriented orbital slot in respectively. The specimen is comparable in its dimendorsal view (Voris et al., 2022) but it is interpreted in this sions to small frontals of Daspletosaurus sp., Gorgowork that this apparent similarity is likely due to the saurus libratus, Tarbosaurus bataar, and Tyrannosaurus "transitional" growth stage that the specimen represents, rex, but much smaller than large frontals of any of these between small juveniles with rostrocaudally elongated (Currie, 2003a; Lehman & Wick, 2013). shallow slot (Carr, 1999; Tsuihiji et al., 2011) and the The subcutaneous surface of the "forehead" region is flat, folded, narrow and deep slot present in tyrannosaurine like in some individuals of Daspletosaurus spp., and in adults (Carr, 2020; Voris et al., 2022), or else as an indi- Lythronax argestes (Voris et al., 2020; Yun, 2020; Figs.
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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.