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FIGURE 4 in Two new species of penicillate millipedes (Diplopoda, Polyxenidae) from Phu Quoc Island in southern Vietnam
FIGURE 4. Holotype Unixenus intragramineus sp. n., A. Head capsule with 8 ommatidia on each side, the posterior vertex trichome groups (pv) and 3 sockets of trichobothria (trichobothria a, b and c). B. Collum (Co) and lateral protuberances (Lp) showing the arrangement of trichome sockets; C. Tergite 2 (T2); D. Tergite 10 – the last tergite; E. trichobothria a, b and c (right hand side) (trichobothrium a, posterior position, trichobothrium b, lateral position and trichobothrium c, anterior position); F. Gnathochilarium: the lateral palp (LP) with 13 sensilla and medial palp (MP) with 22 sensilla; G. Labrum showing the pointed spherical papillae on its surface and the structures 4 + 4 lamellae.
FIGURE 7. A in Two new species of penicillate millipedes (Diplopoda, Polyxenidae) from Phu Quoc Island in southern Vietnam
FIGURE 7. A. Holotype Unixenus intragramineus sp. n., the 2nd leg showing seven leg articles (Co: coxa, pre.fe: prefemur, fe: femur, post.fe: post-femur, tib: tibia, T1: tarsus 1, T2: tarsus 2, C: claw) and sex organ – penis (P); (B) A biarticulated seta with a ridged funicle present on the coxa, prefemur, the distal edge of femur and the posterior edge of last sternite; a similar smaller version of a biarticulated seta with a ridged funicle is present in the middle of the femur (C); seta on tibia (D); the setiform seta on tarsus 2 (E). F. Telotarsus–Claw showing all processes: the anterior lateral process (lp), the posterior process (p), the claw (c), the setiform process (s) and the lamella process (l), SEM image of the telotarsus (right hand side). G. The dorsal ornamental trichome sockets of trichomes a (a), trichome b (b), trichomes c (c) and the circular indentation d.
FIGURE 3 in Two new species of penicillate millipedes (Diplopoda, Polyxenidae) from Phu Quoc Island in southern Vietnam
FIGURE 3. The typical beach habitat of Unixenus intragramineus sp. n. lacking leaf litter. This species was found living within the stem of a creeping grass (Poaceae) growing on an unstable, sandy substrate within the intertidal zone of Tranh River beach, where it is subject to intermittent tidal inundation and is often covered by sand particles. A. The foreshore where U. intragramineus sp. n. was found, the white arrow indicates the grass habitat; B. The grass species showing an aggregation of its runners forming a small clump; C. The grass stems were buried in sand in a beach habitat where no leaf litter was present.
FIGURE 10 in Two new species of penicillate millipedes (Diplopoda, Polyxenidae) from Phu Quoc Island in southern Vietnam
FIGURE 10. Holotype Monographis phuquocensis sp. n., A. The antennal articles V, VI, VII and VIII. B. Arrangement of sensilla on the antennal article VII: A conical sensillum (c) located posteriorly, 2 thick bacilliform sensilla (Tbs) and a setiform sensillum (s). C. Sensilla arrangement on the antennal article VI with 4 groups of sensilla of various lengths: Group 1: 7 bacilliform sensilla, which consists of 3 thick bacilliform sensilla distributed between 1 or 2 thin bacilliform sensilla (Tbs a: Thick bacilliform sensilla located in the anterior position, Tbs i: the thick bacilliform sensilla located in an intermedium position, Tbs p: the thick bacilliform sensilla located in the posterior position); followed by a conical sensillum (c); Group 2: 3 medium length thin bacilliform sensilla (tbs m); Group 3: 2 small thin short bacilliform sensilla (tbs s); Group 4: 8 short thick conical sensilla (Tsc) located posteriorly.
FIGURE 3 in Three new species of Micropsalliota (Agaricaceae, Basidiomycota) from central and southern Vietnam
FIGURE 3. Micropsalliota appendiculata (LE F-315913, holotype): (a) basidiomata in situ: (b) pilei with partial veil, (c) basidiospores, (d) basidia, (e) cheilocystidia, (f) pileipellis hyphae. Bars: a–b = 1 cm; c–e = 10μm; f = 20μm.
FIGURE 2 in Three new species of Micropsalliota (Agaricaceae, Basidiomycota) from central and southern Vietnam
FIGURE 2. Phylogenetic tree of Micropsalliota based on nrLSU sequence data. Bootstrap values over 50% are shown along the branches. Sequences generated for this study are shown in bold. The symbol 'T' refers to type materials.
FIGURE 5 in Three new species of Micropsalliota (Agaricaceae, Basidiomycota) from central and southern Vietnam
FIGURE 5. Micropsalliota suricatoides: (a) basidiomata in situ (LE F-348072, holotype), (b) pilei with umbo (LE F-348069), (c) pileus with umbo (LE F-348070, photo N.V. Psurtseva), (d) basidiospores, (e) basidia, (f) cheilocystidia, (g) pileipellis hyphae. Bars: a–c = 1 cm; d–f = 10 μm; g = 20 μm.
FIGURE 4 in Three new species of Micropsalliota (Agaricaceae, Basidiomycota) from central and southern Vietnam
FIGURE 4. Micropsalliota inflata (LE F-315912, holotype): (a) basidiomata in situ: (b) basidiospores, (c) basidia, (d) cheilocystidia, (e) pileipellis hyphae. Bars: a = 1cm; b–d = 10μm; e = 20μm.
FIGURE 1 in Three new species of Micropsalliota (Agaricaceae, Basidiomycota) from central and southern Vietnam
FIGURE 1. Phylogenetic tree of Micropsalliota based on ITS sequence data. Bootstrap values over 50% are shown along the branches. Sequences generated for this study are shown in bold. The symbol 'T' refers to type materials.
FIGURE 1 in Larval external morphology and chondrocranium of Leptobrachella bidoupensis (Anura: Megophryidae), an endemic litter toad from southern Vietnam
FIGURE 1. External morphology of the Leptobrachella bidoupensis tadpole (ZMMU A-7618, Stage 26, TL 41.6 mm, SVL 15.7 mm): (A) dorsal view; (B), lateral view; (C) oral disc; (D) jaw sheaths; (E) narial ornamentation. (F) Young metamorph (Stage 45, TL 25.5 mm, SVL 18.4 mm). (G) Habitat of L. bidoupensis on Bidoup Mountain, Bidoup–Nui Ba National Park, Vietnam.
FIGURE 2 in Larval external morphology and chondrocranium of Leptobrachella bidoupensis (Anura: Megophryidae), an endemic litter toad from southern Vietnam
FIGURE 2. Larval chondrocranium in Leptobrachella bidoupensis (Stage 26, TL 57.4 mm, SVL 19.5 mm): (A) chondrocranium, dorsal view; (B) lower jaw, frontal view; and (C) hyobranchial apparatus, ventral view. Abbreviations: ac articular condyle, appq ascending process of the palatoquadrate, ar adrostral cartilage, bb basibranchial, cbr ceratobranchials, chy ceratohyal, exo exoccipital bone, hbp hypobranchial plate, irc infrarostral cartilage, Mc Meckel's cartilage, mp muscular process, oc otic capsule, pp posterior process, pq palatoquadrate, pro prootic bone, qcc quadratocranial commissure, sb subocular bar, sp spicule, src suprarostral cartilage, th trabecular horns, ts tectum synoticum, ubp urobranchial process. Scale bar 1 mm.
Subspecies and Distribution. T.n.napuF.Cuvier,1822—SMyanmar,Thai/MalayPeninsula,islandsoffWMalayPeninsula(Langkawi&Pangkor),Borneo,SSumatra,BangkaI,islandsoffBorneo(Laut&Serasan). T.n.bangue:Chasen&Kloss,1931—BanggiIandBalembanganI,offNBorneo. T.n.bunguranensisMiller,1901—NatunaIs(=Bunguran),oftWBorneo. T.n.neubronneriSody,1931—NSumatra. T.n.nmiasisLyon,1916—NiasI,offWSumatra. T.n.rufulusMiller,1900—TiomanI,offEMalayPeninsula,RiauandLinggaArchipelagos. T. n. terutus Thomas & Wroughton, 1909 — Terutau I, off W Malay Peninsula. The species was recently reconfirmed for Singapore. Maps that include Vietnam, Cambodia, and Laos in the distribution range are based on the earlier assumption that 7. versicolor was a subspecies of 1. napu. Subsequent studies have indicated that 7. versicolor is a distinct species, and that the range of 1. napu therefore does not extend into Cambodia, Laos, and Vietnam. The northern limit on the Thai-Malay peninsula is not well defined. Specimens of 1. napu have been collected from as far north as Bankachon in southern Myanmar (10° 08" N), but despite fairly intensive camera-trapping in Kui Buri National Park, Thailand (12° N), 7. napu has not been photographed there. At the northern margin ofits range, it is generally rare. It has been reported, for example, that during the flooding of the Chiew Larn Reservoir (Surat Thani Province; about 9° N, 98° 45' E), only six 7. napu were rescued compared with 172 71. kanchil. This area is the transition zone from wetter evergreen forest to drier deciduous types, and it might be that 7° napu is not well adapted to the drier forest types towards the northern limit ofits range. There are unconfirmed reports of the species on Java, where it may have been confused with one of the two color morphs of 7. javanicus. As explained in the Taxonomy section, the subspecific status of the populations of several islands remains unclear. in Tragulidae
Subspecies and Distribution. T.n.napuF.Cuvier,1822—SMyanmar,Thai/MalayPeninsula,islandsoffWMalayPeninsula(Langkawi&Pangkor),Borneo,SSumatra,BangkaI,islandsoffBorneo(Laut&Serasan). T.n.bangue:Chasen&Kloss,1931—BanggiIandBalembanganI,offNBorneo. T.n.bunguranensisMiller,1901—NatunaIs(=Bunguran),oftWBorneo. T.n.neubronneriSody,1931—NSumatra. T.n.nmiasisLyon,1916—NiasI,offWSumatra. T.n.rufulusMiller,1900—TiomanI,offEMalayPeninsula,RiauandLinggaArchipelagos. T. n. terutus Thomas & Wroughton, 1909 — Terutau I, off W Malay Peninsula. The species was recently reconfirmed for Singapore. Maps that include Vietnam, Cambodia, and Laos in the distribution range are based on the earlier assumption that 7. versicolor was a subspecies of 1. napu. Subsequent studies have indicated that 7. versicolor is a distinct species, and that the range of 1. napu therefore does not extend into Cambodia, Laos, and Vietnam. The northern limit on the Thai-Malay peninsula is not well defined. Specimens of 1. napu have been collected from as far north as Bankachon in southern Myanmar (10° 08" N), but despite fairly intensive camera-trapping in Kui Buri National Park, Thailand (12° N), 7. napu has not been photographed there. At the northern margin ofits range, it is generally rare. It has been reported, for example, that during the flooding of the Chiew Larn Reservoir (Surat Thani Province; about 9° N, 98° 45' E), only six 7. napu were rescued compared with 172 71. kanchil. This area is the transition zone from wetter evergreen forest to drier deciduous types, and it might be that 7° napu is not well adapted to the drier forest types towards the northern limit ofits range. There are unconfirmed reports of the species on Java, where it may have been confused with one of the two color morphs of 7. javanicus. As explained in the Taxonomy section, the subspecific status of the populations of several islands remains unclear.
Distribution. Thailand and southern China, mainly the Sanchahe part of the Mengman region and the Darongshu of the Longmen region, both in S. Yunnan, but possibly more widespread with potential presence in Laos, Vietnam, and Myanmar. in Tragulidae
Distribution. Thailand and southern China, mainly the Sanchahe part of the Mengman region and the Darongshu of the Longmen region, both in S. Yunnan, but possibly more widespread with potential presence in Laos, Vietnam, and Myanmar.
FIGURE 3. Typhonium khonkaenensis. A in A new species and a new record of Typhonium (Araceae) from southern Vietnam
FIGURE 3. Typhonium khonkaenensis. A. The species in habitat. B. Whole plant. C. Different forms of leaf blade. D. Inflorescence. E. Spathe. F. Part of spadix showing male, sterile and female zones. G. Spathe, inside. H. Stamens. I. Female flowers. J. Fruits. K. Seeds.
FIGURE 1. Typhonium vietnamense. A in A new species and a new record of Typhonium (Araceae) from southern Vietnam
FIGURE 1. Typhonium vietnamense. A. The species in habitat. B. Whole plant. C. Different forms of leaf blade. D & E. Spathe. F. Longitudinal section of inflorescence. G. Male zone. H. Female zone and staminodes. I. Ovaries. J. Stigmas. K. Stamens. L. Fruits. M. Seeds.
FIGURE 2. Peliosanthes luteoviridis. A. Habit. B, C in Peliosanthes luteoviridis (Asparagaceae), a new species with yellowish green flowers from southern Vietnam
FIGURE 2. Peliosanthes luteoviridis. A. Habit. B, C. Part of foliage leaf, adaxial (B) and abaxial (C) views. D. Fruiting inflorescence (showing seeds). E. Flower, view from below. F. Flower, top view. G, H. Inflorescences. I. Portion of inflorescence. Photos by T.T.D. Pham & K.S. Nguyen from Nguyen Sinh Khang et al. NSK 1354B-1, NSK 1354B-2; correction and design by N. Vislobokov.
FIGURE 1. Peliosanthes luteoviridis. A. Habit. B. Foliage leaf, adaxial view. C. Inflorescences. D, E in Peliosanthes luteoviridis (Asparagaceae), a new species with yellowish green flowers from southern Vietnam
FIGURE 1. Peliosanthes luteoviridis. A. Habit. B. Foliage leaf, adaxial view. C. Inflorescences. D, E. Portions of inflorescence. F. Flower, side view. G. Flower, longitudinal section. Photos: A, B by N.A. Vislobokov from Vislobokov 19203; C‒G by M.S. Romanov from 2019.15598; correction and design by N.A. Vislobokov.
FIGURE. Fruiting heads and peduncles of C. spongifolia. A. Site WP260; two peduncles have lost heads (arrows 1 and 2), the upper part (male zone) of one spadix lies on ground (arrow 3), and six attached heads all touch ground. B–E. Site WP251; a single, detached immature head with bite marks in upper and lower ends, and torn surface at junction with peduncle (at left in D–E). Scale bars: 10 cm with 1 cm units (main image); 8 cm with 2 cm units (lower right); B–C enlarged, without scale. (Bach Ma NP, 2018). Photos: PJM. in Colocasia spongifolia sp. nov. (Araceae) in southern China and central Vietnam
FIGURE. Fruiting heads and peduncles of C. spongifolia. A. Site WP260; two peduncles have lost heads (arrows 1 and 2), the upper part (male zone) of one spadix lies on ground (arrow 3), and six attached heads all touch ground. B–E. Site WP251; a single, detached immature head with bite marks in upper and lower ends, and torn surface at junction with peduncle (at left in D–E). Scale bars: 10 cm with 1 cm units (main image); 8 cm with 2 cm units (lower right); B–C enlarged, without scale. (Bach Ma NP, 2018). Photos: PJM.
FIGURE. Floral habit and structure of C. spongifolia. A. Type specimen in situ with open, spathe limb (apex is reflexed out of view), and green spathe tube (ca. 6 cm long). B. Adjacent plant with inflorescences and prophylls. C. Spadix showing from top: sterile appendix, staminate (male) zone, sterile interstice, and green pistillate (female) zone with tapered, conical form. D. Detail of female zone showing a few basal staminodes. E–G. Berries of the preserved type specimen. G. Dissected berry with orthotropous ovules (some outlined) attached by funicles to parietal placentae (arrows). H. Surface of male zone showing closely-packed synandria. I. Synandria separated to show fused anther sacs beneath apical pores (example in center has 8 pores, 8 anthers) J. Mature fruiting head, with single berry removed to show seed packing and 67 seeds extracted (scale bar units: 1 mm) (Bach Ma NP; type 2020; fruit and seeds 2018). Photos: NVD and PJM. in Colocasia spongifolia sp. nov. (Araceae) in southern China and central Vietnam
FIGURE. Floral habit and structure of C. spongifolia. A. Type specimen in situ with open, spathe limb (apex is reflexed out of view), and green spathe tube (ca. 6 cm long). B. Adjacent plant with inflorescences and prophylls. C. Spadix showing from top: sterile appendix, staminate (male) zone, sterile interstice, and green pistillate (female) zone with tapered, conical form. D. Detail of female zone showing a few basal staminodes. E–G. Berries of the preserved type specimen. G. Dissected berry with orthotropous ovules (some outlined) attached by funicles to parietal placentae (arrows). H. Surface of male zone showing closely-packed synandria. I. Synandria separated to show fused anther sacs beneath apical pores (example in center has 8 pores, 8 anthers) J. Mature fruiting head, with single berry removed to show seed packing and 67 seeds extracted (scale bar units: 1 mm) (Bach Ma NP; type 2020; fruit and seeds 2018). Photos: NVD and PJM.
FIGURE. Stem, roots, and buds of C. spongifolia. A. Cross section of stem in B, showing clear, gummy exudate. B. Mature stem with decumbent part at left, erect part at right, roots and rootlets, brown leaf scars, and single adaxial buds (arrows). C. Young stem, with single, adaxial bud revealed. Scale bars = 2 cm (Bach Ma NP, 2018, 2021). Photos: NVD and PJM. in Colocasia spongifolia sp. nov. (Araceae) in southern China and central Vietnam
FIGURE. Stem, roots, and buds of C. spongifolia. A. Cross section of stem in B, showing clear, gummy exudate. B. Mature stem with decumbent part at left, erect part at right, roots and rootlets, brown leaf scars, and single adaxial buds (arrows). C. Young stem, with single, adaxial bud revealed. Scale bars = 2 cm (Bach Ma NP, 2018, 2021). Photos: NVD and PJM.
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Allen Brain Atlas
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DANDI Archive for NWB datasets
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International Brain Laboratory public data
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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.