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F I G U R E 2 in Current progress and future prospects for understanding genetic diversity of seed plants in China
F I G U R E 2 Number of articles on genetic diversity for seed plants in different fields. The data comes from the results of Web of Science (www.webofscience.com/wos/alldb/basic‐search, accessed: January 17th, 2024) using the search rule: TS = (seed plant genetic diversity) OR TS = (flowering plant genetic diversity) OR TS = (germplasm genetic diversity) OR TS = (angiosperm genetic diversity) OR TS = (gymnosperm genetic diversity). The numbers in parentheses represent the number of articles published in different fields. The overlapping areas show studies that cover multiple fields.
F I G U R E 1 A in A healing place: Reimagining the modern botanic garden as a physic garden
F I G U R E 1 A modern "physic garden," as I have described here: Royal Botanic Gardens Melbourne (Melbourne Gardens), one of two botanic gardens managed by Royal Botanic Gardens Victoria. Photo: Royal Botanic Gardens Victoria, July 2020.
F I G U R E 1 in Current progress and future prospects for understanding genetic diversity of seed plants in China
F I G U R E 1 Number of articles on genetic diversity in different sequencing stages, with lines of red, blue, and green representing studies for all organisms, plants, and seed plants, respectively. Molecular markers and their first published time are provided in the blue boxes. Three major public databases (NCBI, EMBL, and BioSino) and their established time are shown in the red boxes. The data comes from the results of Web of Science (www.webofscience.com/wos/alldb/basic‐search, accessed: January 17th, 2024) using the search rules: TS = (genetic diversity) for all, TS = (plants genetic diversity) OR TS = (ferns genetic diversity) OR TS = (moss genetic diversity) OR TS = (angiosperm genetic diversity) OR TS = (gymnosperm genetic diversity) for plants, and TS = (seed plant genetic diversity) OR TS = (flowering plant genetic diversity) OR TS = (germplasm genetic diversity) OR TS = (angiosperm genetic diversity) OR TS = (gymnosperm genetic diversity) for seed plants.
PLATE IVA. Metioche Stal, 1877. (A–J), Metioche japonica (Ichikawa, 2001): A, Male; B, Inner margin of eyes more brightlyrimmed; C, Male sub-genital plate; D, Fore tibiae without tympanum on both sides; E, Shape of last segment of maxillary palpi-securiform; F, Male genitalia; G, Female; H, Tegmina convex; I, Female ovipositor upturned, shaped; apex sharp with teeth on; J, subgenital plate triangular. in JHABAR MAL, RAJENDRA NAGAR & R. SWAMINATHAN (2014) Record of Natula matsuurai Sugimoto (Orthoptera: Gryllidae: Trigonidiinae) and other sword-tailed crickets from India. Zootaxa, 3760(3): 458-462.
PLATE IVA. Metioche Stal, 1877. (A–J), Metioche japonica (Ichikawa, 2001): A, Male; B, Inner margin of eyes more brightlyrimmed; C, Male sub-genital plate; D, Fore tibiae without tympanum on both sides; E, Shape of last segment of maxillary palpi-securiform; F, Male genitalia; G, Female; H, Tegmina convex; I, Female ovipositor upturned, shaped; apex sharp with teeth on; J, subgenital plate triangular.
PLATE III. Trigonidium Rambur, 1839. (A–H), Trigonidium humbertianum (Saussure, 1878): A, Male; B, Female; C, Eyesrounded protruding; D–E, Fifth joint of maxillary palpi large and triangular; F, Anterior tibiae with tympanum on both sides; G, Female ovipositor curved, compressed, acute at apex; H, Male sub-genital plate feebly notched at apex. in JHABAR MAL, RAJENDRA NAGAR & R. SWAMINATHAN (2014) Record of Natula matsuurai Sugimoto (Orthoptera: Gryllidae: Trigonidiinae) and other sword-tailed crickets from India. Zootaxa, 3760(3): 458-462.
PLATE III. Trigonidium Rambur, 1839. (A–H), Trigonidium humbertianum (Saussure, 1878): A, Male; B, Female; C, Eyesrounded protruding; D–E, Fifth joint of maxillary palpi large and triangular; F, Anterior tibiae with tympanum on both sides; G, Female ovipositor curved, compressed, acute at apex; H, Male sub-genital plate feebly notched at apex.
PLATE IIB. Paratrigonidium Brunner, 1893. (A–E), Paratrigonidium nitidum Brunner, 1893: A, Male elytra membranous & harpvein only one; B, Palpi long, yellowish, fifth joint of maxillary palpi long, feebly widening at apex; C, Lateral field of tegmina inmale blackish, presenting 3 parallel veins and the fourth incomplete; D, The hind femur with a feeble brownish band/stripe; E, The female ovipositor fulvous at base, darkened in the middle. Trigonidium Rambur, 1839. (F–I), Trigonidium humbertianum (Saussure, 1878): F, Anterior tibiae with tympanum on both sides; G, Fifth joint of maxillary palpi large and triangular; H, Female ovipositor curved, compressed, acute at apex; I, Male sub-genital plate feebly notched at apex. in JHABAR MAL, RAJENDRA NAGAR & R. SWAMINATHAN (2014) Record of Natula matsuurai Sugimoto (Orthoptera: Gryllidae: Trigonidiinae) and other sword-tailed crickets from India. Zootaxa, 3760(3): 458-462.
PLATE IIB. Paratrigonidium Brunner, 1893. (A–E), Paratrigonidium nitidum Brunner, 1893: A, Male elytra membranous & harpvein only one; B, Palpi long, yellowish, fifth joint of maxillary palpi long, feebly widening at apex; C, Lateral field of tegmina inmale blackish, presenting 3 parallel veins and the fourth incomplete; D, The hind femur with a feeble brownish band/stripe; E, The female ovipositor fulvous at base, darkened in the middle. Trigonidium Rambur, 1839. (F–I), Trigonidium humbertianum (Saussure, 1878): F, Anterior tibiae with tympanum on both sides; G, Fifth joint of maxillary palpi large and triangular; H, Female ovipositor curved, compressed, acute at apex; I, Male sub-genital plate feebly notched at apex.
PLATE IIA. Paratrigonidium Brunner, 1893. (A–K), Paratrigonidium nitidum Brunner, 1893: A–B, Male and female black, shining;the male with membranous elytra, while female elytra corneous, convex with plain, longitudinal veins. Vertex flattened and sloping; C, Head wide and black; antenae yellow with first joint black; D, Pronotum black, pubescent; E, Palpi long, yellowish, fifth joint of maxillary palpi long, feebly widening at apex; F, Tympanum external; G, Male elytra membranous; H, The hind femurwith a feeble brownish band/stripe; I, Legs yellowish; J, Lateral field of tegmina in male blackish, presenting 3 parallel veins andthe fourth incomplete; K, The female ovipositor fulvous at base, darkened in the middle, cerci long. in JHABAR MAL, RAJENDRA NAGAR & R. SWAMINATHAN (2014) Record of Natula matsuurai Sugimoto (Orthoptera: Gryllidae: Trigonidiinae) and other sword-tailed crickets from India. Zootaxa, 3760(3): 458-462.
PLATE IIA. Paratrigonidium Brunner, 1893. (A–K), Paratrigonidium nitidum Brunner, 1893: A–B, Male and female black, shining;the male with membranous elytra, while female elytra corneous, convex with plain, longitudinal veins. Vertex flattened and sloping; C, Head wide and black; antenae yellow with first joint black; D, Pronotum black, pubescent; E, Palpi long, yellowish, fifth joint of maxillary palpi long, feebly widening at apex; F, Tympanum external; G, Male elytra membranous; H, The hind femurwith a feeble brownish band/stripe; I, Legs yellowish; J, Lateral field of tegmina in male blackish, presenting 3 parallel veins andthe fourth incomplete; K, The female ovipositor fulvous at base, darkened in the middle, cerci long.
PLATE IVB. Metioche Stal, 1877. (A–G), Metioche japonica (Ichikawa, 2001): A, Eyes rounded, large and widely separated; B,Antennae: Scape and pedicel dark black, flagellum light in colour; C, Shape of last segment of maxillary palpi-securiform; D, Female sub-genital plate triangular; E, Male sub-genital plate; F, Male genitalia; G, Female ovipositor upturned, sabre shaped; apexsharp with teeth on ventre. in JHABAR MAL, RAJENDRA NAGAR & R. SWAMINATHAN (2014) Record of Natula matsuurai Sugimoto (Orthoptera: Gryllidae: Trigonidiinae) and other sword-tailed crickets from India. Zootaxa, 3760(3): 458-462.
PLATE IVB. Metioche Stal, 1877. (A–G), Metioche japonica (Ichikawa, 2001): A, Eyes rounded, large and widely separated; B,Antennae: Scape and pedicel dark black, flagellum light in colour; C, Shape of last segment of maxillary palpi-securiform; D, Female sub-genital plate triangular; E, Male sub-genital plate; F, Male genitalia; G, Female ovipositor upturned, sabre shaped; apexsharp with teeth on ventre.
PLATE IB. Natula Gorochov, 1987. (A–K), Natula matsuurai (Sugimoto, 2001): A, Head; B, Maxillary palpi; C, Second tarsal segment; D, Tympanum on fore tibia; E, Forewing lateral view showing longitudinal veins; F, Hind femur without stripe; G, Male Forewing mirror longer than wide; H, Female sub-genital plate triangular; I, Male sub-genital plate longer than wide, hind margin with a small projected median lobe; J, Hind tibial spines (3 pairs) on both sides; K, Ovipositor upcurved with a dorsal groove in JHABAR MAL, RAJENDRA NAGAR & R. SWAMINATHAN (2014) Record of Natula matsuurai Sugimoto (Orthoptera: Gryllidae: Trigonidiinae) and other sword-tailed crickets from India. Zootaxa, 3760(3): 458-462.
PLATE IB. Natula Gorochov, 1987. (A–K), Natula matsuurai (Sugimoto, 2001): A, Head; B, Maxillary palpi; C, Second tarsal segment; D, Tympanum on fore tibia; E, Forewing lateral view showing longitudinal veins; F, Hind femur without stripe; G, Male Forewing mirror longer than wide; H, Female sub-genital plate triangular; I, Male sub-genital plate longer than wide, hind margin with a small projected median lobe; J, Hind tibial spines (3 pairs) on both sides; K, Ovipositor upcurved with a dorsal groove
PLATE IA. Natula Gorochov, 1987. (A–L), Natula matsuurai (Sugimoto, 2001): A, Male; B, Female; C, Face with a transverse dark strip near epistomal suture; D, Fifth joint of maxillary palpi hatchet shaped; E, Lateral field of tegmina deeper than lateral lobe of pronotum; F, Hind tibia with 3 pairs of dorsal spines on both sides but largest inner apical spurs as long as or half of basitarsus; G, Fore tibia with oval shaped outer and inner tympanum; H, Harp vein only one, Mirror area occupying half dorsal surface, not divided with a small concentric inner veinlet; I, Pronotum with roundly convex anterior margin; J, Female ovipositor strongly upcurved, half as long as hind femur, three fifth area from base widened and bumpy, with a dorsal groove, cerci as long as ovipositor; K, Male sub-genital plate longer than wide, hind margin narrowly truncated with a small projected median lobe, two styli present; L, Female sub-genital plate roundly triangular. in JHABAR MAL, RAJENDRA NAGAR & R. SWAMINATHAN (2014) Record of Natula matsuurai Sugimoto (Orthoptera: Gryllidae: Trigonidiinae) and other sword-tailed crickets from India. Zootaxa, 3760(3): 458-462.
PLATE IA. Natula Gorochov, 1987. (A–L), Natula matsuurai (Sugimoto, 2001): A, Male; B, Female; C, Face with a transverse dark strip near epistomal suture; D, Fifth joint of maxillary palpi hatchet shaped; E, Lateral field of tegmina deeper than lateral lobe of pronotum; F, Hind tibia with 3 pairs of dorsal spines on both sides but largest inner apical spurs as long as or half of basitarsus; G, Fore tibia with oval shaped outer and inner tympanum; H, Harp vein only one, Mirror area occupying half dorsal surface, not divided with a small concentric inner veinlet; I, Pronotum with roundly convex anterior margin; J, Female ovipositor strongly upcurved, half as long as hind femur, three fifth area from base widened and bumpy, with a dorsal groove, cerci as long as ovipositor; K, Male sub-genital plate longer than wide, hind margin narrowly truncated with a small projected median lobe, two styli present; L, Female sub-genital plate roundly triangular.
FIG. 5. — A-E, G, I-K in Two new species of Collembola (Hexapoda) from Saliente Cave (Almería, Spain)
FIG. 5. — A-E, G, I-K, Pseudosinella najtae Jordana & Baquero, n. sp.: labrum showing the ciliated chaetae (A); labium chaetotaxy (B); head chaetotaxy (the nomenclature follows Gisin & Da Gama 1969, and in brackets Soto-Adames (2010) (C); Ant. II–IV (D); claw (E); male genital complex (G); dens end and mucro (I); Abd. II–IV chaetotaxy (J); Abd. IV macrochaeta B5 (K); F, H, Pseudosinella infrequens Gisin & Da Gama, 1969 (drawings from holotype): claw and empodium (F); dens end and mucro (H). Scale bars: A, 4 μm; B, 15 μm; C, D, G, I, 20 μm; E, 10 μm.
FIG. 6. —A-C, E-G, Deutonura jeromoltoi n in Two new species of Poduromorpha (Collembola) from the Mercantour National Park (Alpes-Maritimes, France), with comments on pseudopore patterns
FIG. 6. —A-C, E-G, Deutonura jeromoltoi n. sp.; D, D. gibbosa Porco, Bedos & Deharveng, 2010: A, dorsal chaetotaxy, Black spots, pseudopores; B, labrum chaetotaxy; C, ventro-distal sclerification of labrum in D. jeromoltoi n. sp.; D, idem in D. gibbosa; E, labium; F, left Ant. III-IV in dorsal view; G, left Ant. III-IV in ventral view. Names of antennal chaetae after Smolis, 2008. Scale bars: A, 100 µm; B-E, 20 µm.
BRACHYDERINAE AND OTIORHYNCHINAE. A, TRIGONOPS IMPURA; B, VITICIS GUAMAI!.; C, TRJGONOPS INCRJNITA; D, T. HIRSUTA; E, T. INAEQUALIS, HOLOTYPE MALE; F, T. /NUS/TATA; G, T. VULGARJS; B, T. INAF.QUALIS, FEMALE; I, T. CONVEXA. (PHOTOGRAPHS BY W. TWIGG-SMiffl.) in Curculionidae of Guam
BRACHYDERINAE AND OTIORHYNCHINAE. A, TRIGONOPS IMPURA; B, VITICIS GUAMAI!.; C, TRJGONOPS INCRJNITA; D, T. HIRSUTA; E, T. INAEQUALIS, HOLOTYPE MALE; F, T. /NUS/TATA; G, T. VULGARJS; B, T. INAF.QUALIS, FEMALE; I, T. CONVEXA. (PHOTOGRAPHS BY W. TWIGG-SMiffl.)
FrGURI> 1.-it-e, Scatopse g11amensis: a, wing of female X 34; b, clasper of male X 225; c, hypopygium of male, ventral aspect X 45 (a, mesosome, c, clasper); d, mesosome of male, ventral aspect X 225; e, terminalia of female, ventral aspect X 225. f, g, Psectrosciara breviconiis: f, wing of female X 45; g, antennae of female X 225. h, Culicoides guttifer deMeijere, var. histrio, inner processes of male; caudal end directed downward X 225. i, Eukraiohelea inusitata, wing of female X 24. j, Smittia insitlsa, ventral aspect of half of hypopygium X 225. k, Chironomus insolens, ventral aspect of half of hypopygium X 112. 1, Chironomus eximiiis, latero-ventral aspect of half of hypopygium X 225 in Some New Species Of Nemocerous Diptera From Guam
FrGURI> 1.-it-e, Scatopse g11amensis: a, wing of female X 34; b, clasper of male X 225; c, hypopygium of male, ventral aspect X 45 (a, mesosome, c, clasper); d, mesosome of male, ventral aspect X 225; e, terminalia of female, ventral aspect X 225. f, g, Psectrosciara breviconiis: f, wing of female X 45; g, antennae of female X 225. h, Culicoides guttifer deMeijere, var. histrio, inner processes of male; caudal end directed downward X 225. i, Eukraiohelea inusitata, wing of female X 24. j, Smittia insitlsa, ventral aspect of half of hypopygium X 225. k, Chironomus insolens, ventral aspect of half of hypopygium X 112. 1, Chironomus eximiiis, latero-ventral aspect of half of hypopygium X 225
Fig. 8. Male genitalia. A, C, E, G, I, K. Dorsal view. B, D, F, H, J, L. Ventral view. A–B in Description of four new species of the subgenus Tachycines (Gymnaeta) Adelung, 1902 (Orthoptera: Rhaphidophoridae) from caves in China and additional notes on some previously known species
Fig. 8. Male genitalia. A, C, E, G, I, K. Dorsal view. B, D, F, H, J, L. Ventral view. A–B. Tachycines (Gymnaeta) quadratus sp. nov., holotype, ♂ (HBU). C–D. Tachycines (Gymnaeta) shiziensis sp. nov., holotype, ♂ (HBU). E–F. Tachycines (Gymnaeta) sparsispinus sp. nov., holotype, ♂ (HBU). G–H. Tachycines (Gymnaeta) papilious sp. nov., holotype, ♂ (HBU). I–J. Tachycines (Gymnaeta) latellai (Rampini & Di Russo, 2008), ♂. K–L. Tachycines (Gymnaeta) omninocaecus (Gorochov, Rampini & Di Russo, 2006), ♂.
Raw data for the article: Human Amnion Epithelial Cells Impair T Cell Proliferation: The Role of HLA-G and HLA-E Molecules
<p>The immunoprivilege status characteristic of human amnion epithelial cells (hAECs) has been recently highlighted in the context of xenogenic transplantation. However, the mechanism(s) involved in such regulatory functions have been so far only partially been clarified. Here, we have analyzed the expression of HLA-Ib molecules in isolated hAEC obtained from full term placentae. Moreover, we asked whether these molecules are involved in the immunoregulatory functions of hAEC. Human amnion-derived cells expressed surface HLA-G and HLA-F at high levels, whereas the commonly expressed HLA-E molecule has been measured at a very low level or null on freshly isolated cells. HLA-Ib molecules can be expressed as membrane-bound and soluble forms, and in all hAEC batches analyzed we measured high levels of sHLA-G and sHLA-E when hAEC were maintained in culture, and such a release was time-dependent. Moreover, HLA-G was present in extracellular vesicles (EVs) released by hAEC. hAEC suppressed T cell proliferation in vitro at different hAEC:T cell ratios, as previously reported. Moreover, inhibition of T cell proliferation was partially reverted by pretreating hAEC with anti-HLA-G, anti-HLA-E and anti-β2 microglobulin, thus suggesting that HLA-G and -E molecules are involved in hAEC-mediated suppression of T cell proliferation. Finally, either large-size EV (lsEV) or small-size EV (ssEV) derived from hAEC significantly modulated T-cell proliferation. In conclusion, we have here characterized one of the mechanism(s) underlying immunomodulatory functions of hAEC, related to the expression and release of HLA-Ib molecules.</p>
Fig. 35. A–E, Pseudosesarma crassimanum. A–G in Revision of the intertidal and semiterrestrial crab genera Chiromantes Gistel, 1848, and Pseudosesarma Serène & Soh, 1970 (Crustacea: Brachyura: Sesarmidae), using morphology and molecular phylogenetics, with the establishment of nine new genera and two new species
Fig. 35. A–E, Pseudosesarma crassimanum. A–G, lectotype male (16.3 × 14.6 mm) (NHM 1886.52b), Myanmar; H–M, male (15.9 × 14.3 mm) (ZRC 2008.0442), Ranong; N–R, male (15.9 × 14.5 mm) (RMNH-D23313), Singapore. A, N, pleon; B–F, right G1; G, right G2; H–L, O–R, left G1; M, left G2. Scales: A = 2.0 mm; B, G, H, I, M, O, P = 1.0 mm; N = 5.0 mm; C–F, J–L, Q, R = 0.5 mm. After Ng & Schubart (2017: fig. 11).
FIGURE 5. Chiropteran mandibles. A. Mormoops blainvillei, B. Pteronotus macleayii, C. Pteronotus parnellii, D. Pteronotus quadridens, E. Brachyphylla nana, F. Erophylla bombifrons, G. Monophyllus redmani, H in Quaternary Bat Diversity in the Dominican Republic
FIGURE 5. Chiropteran mandibles. A. Mormoops blainvillei, B. Pteronotus macleayii, C. Pteronotus parnellii, D. Pteronotus quadridens, E. Brachyphylla nana, F. Erophylla bombifrons, G. Monophyllus redmani, H. Phyllonycteris poeyi. Scale bar = 5 mm.
Text-fig. 8. a, o – Miostrellus petersbuchensis, Petersbuch 28: a – NMA P28/0335, right maxillary bone with P4–M3, holotype, ventral view; o – NMA P28/0449, right mnd with C inf., p4–m3, occlusal view; b–f, k, n – M. cf. noctuloides: b – BSP 1962 XIX 4198, right M3, Erkertshofen 1, occlusal view; c – BSP 1962 XIX 4195, left M1, Erkertshofen 1, occlusal view; d – PCMRCh4, left C sup., Petersbuch 2, lingual (d1) and occlusal (d2) views; e – BSP 1974 XIV 1204, left C sup., Erkertshofen 2, occlusal (e1) and lingual (e2) views; f – PCMRCh23, right P4, Petersbuch 2, occlusal view; k – BSP 1974 XIV 1200, right C inf., Erkertshofen 2, occlusal view; n – BSP 1962 XIX 4192, right mnd with m1–2; Erkertshofen 1, lateral (n1) and occlusal (n2) views; g – Eptesicus cf. aurelianensis, BSP 1962 XIX 4197, right M2, Erkertshofen 1, occlusal view; h, i – cf. Miostrellus sp., Erkertshofen 2: h – BSP 1974 XIV 1203, left m1, occlusal view; i – BSP 1974 XIV 1207, right P4; j, l, m – Miostrellus cf. petersbuchensis, Petersbuch 2, occlusal views: j – PCMRCh5, left m1; l – PCMRCh7, left p4; m – PCMRCh6, right mnd with m1. in The Early Miocene Bats (Chiroptera, Mammalia) From The Karstic Sites Of Erkertshofen And Petersbuch 2 (Southern Germany)
Text-fig. 8. a, o – Miostrellus petersbuchensis, Petersbuch 28: a – NMA P28/0335, right maxillary bone with P4–M3, holotype, ventral view; o – NMA P28/0449, right mnd with C inf., p4–m3, occlusal view; b–f, k, n – M. cf. noctuloides: b – BSP 1962 XIX 4198, right M3, Erkertshofen 1, occlusal view; c – BSP 1962 XIX 4195, left M1, Erkertshofen 1, occlusal view; d – PCMRCh4, left C sup., Petersbuch 2, lingual (d1) and occlusal (d2) views; e – BSP 1974 XIV 1204, left C sup., Erkertshofen 2, occlusal (e1) and lingual (e2) views; f – PCMRCh23, right P4, Petersbuch 2, occlusal view; k – BSP 1974 XIV 1200, right C inf., Erkertshofen 2, occlusal view; n – BSP 1962 XIX 4192, right mnd with m1–2; Erkertshofen 1, lateral (n1) and occlusal (n2) views; g – Eptesicus cf. aurelianensis, BSP 1962 XIX 4197, right M2, Erkertshofen 1, occlusal view; h, i – cf. Miostrellus sp., Erkertshofen 2: h – BSP 1974 XIV 1203, left m1, occlusal view; i – BSP 1974 XIV 1207, right P4; j, l, m – Miostrellus cf. petersbuchensis, Petersbuch 2, occlusal views: j – PCMRCh5, left m1; l – PCMRCh7, left p4; m – PCMRCh6, right mnd with m1.
Text-fig. 7. a–e, h, i – Myotis cf. reductus: a – BSP 1974 XIV 1209, left M2, Erkertshofen 2, occlusal view; b – BSP 1974 XIV 1208, right M1, Erkertshofen 2, occlusal view; c – left maxillary fragment with M1–2, NMA P28/0345, Petersbuch 28, ventral view; d – BSP 1974 XIV 1199, left C inf., Erkertshofen 2, lingual (c1) and occlusal (c2) views; e – SNSB-BSPG 1962 XIX 4200, left mnd without teeth; Erkertshofen 1, occlusal (e1) and lateral (e2) views; h – BSP 1974 XIV 1202, left p4, Erkertshofen 2, occlusal view; i – PCMRCh87, right m3, Petersbuch 2, occlusal view; f, g – cf. Myotis sp., right C inf., Petersbuch 2, lingual view: f – PCMRCh25, g – PCMRCh88; j – M. aff. reductus, NMA P62/0331, right dentary fragment with p4–m1, Petersbuch 62, occlusal view. in The Early Miocene Bats (Chiroptera, Mammalia) From The Karstic Sites Of Erkertshofen And Petersbuch 2 (Southern Germany)
Text-fig. 7. a–e, h, i – Myotis cf. reductus: a – BSP 1974 XIV 1209, left M2, Erkertshofen 2, occlusal view; b – BSP 1974 XIV 1208, right M1, Erkertshofen 2, occlusal view; c – left maxillary fragment with M1–2, NMA P28/0345, Petersbuch 28, ventral view; d – BSP 1974 XIV 1199, left C inf., Erkertshofen 2, lingual (c1) and occlusal (c2) views; e – SNSB-BSPG 1962 XIX 4200, left mnd without teeth; Erkertshofen 1, occlusal (e1) and lateral (e2) views; h – BSP 1974 XIV 1202, left p4, Erkertshofen 2, occlusal view; i – PCMRCh87, right m3, Petersbuch 2, occlusal view; f, g – cf. Myotis sp., right C inf., Petersbuch 2, lingual view: f – PCMRCh25, g – PCMRCh88; j – M. aff. reductus, NMA P62/0331, right dentary fragment with p4–m1, Petersbuch 62, occlusal view.
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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
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