Find research datasets worth reusing

opennotspecifiedDec 2014View details →

FIGURES 18–21 in Comparative morphology and taxonomy of Sciacharis s. str., Chathamaenus Franz and Maorinus Franz (Coleoptera: Staphylinidae: Scydmaeninae)

FIGURES 18–21. Pterothorax in ventral view: Sciacharis (s. str.) fulva Broun (18); Sciacharis (s. str.) chathamensis (Franz), comb. n. with (19) and without (20) setation; Sciacharis (Maorinus) sp. (21). Abbreviations: ar, anterior ridge; lmfa, lateral mesofurcal arm; mcp, mesocoxal projection; mff, mesofurcal fovea; mscc, mesocoxal cavity; msvp, mesoventral intercoxal process; mtvp, metaventral intercoxal process; pl, posterior lobe; pre, prepectus; si, setose impression; v3, metaventrite; vlf, ventrolateral foveae.

opennotspecifiedAug 2011View details →

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.

FIGURE 2 in Comparative morphology and taxonomy of the tiger moth genus Epanycles Butler (Lepidoptera, Erebidae, Arctiinae, Arctiini, Ctenuchina), with notes on related genera

FIGURE 2. Male and female genitalia of Epanycles imperialis. A) Male genitalia, dorsal view; B) Same, lateral view; C) Same, posterior view; D) Aedeagus; E) Female genitalia, dorsal view; F) Same, lateral view. Scale bars: 1 mm.

FIGURE 3 in Comparative morphology and taxonomy of the tiger moth genus Epanycles Butler (Lepidoptera, Erebidae, Arctiinae, Arctiini, Ctenuchina), with notes on related genera

FIGURE 3. Male and female genitalia of Hyaleucerea gigantea. A) Male genitalia, dorsal view; B) Same, lateral view; C) Same, posterior view; D) Aedeagus; E) Female genitalia, lateral view; F) Same, dorsal view; G) Same, ventral view. Scale bars: 1 mm.

FIGURE 5 in Comparative morphology and taxonomy of the tiger moth genus Epanycles Butler (Lepidoptera, Erebidae, Arctiinae, Arctiini, Ctenuchina), with notes on related genera

FIGURE 5. Male and female genitalia of Sciopsyche tropica. A) Male genitalia, dorsal view; B) Same, lateral view; C) Same, posterior view; D) Aedeagus; E) Female genitalia, lateral view; F) Same, dorsal view; G) Same, ventral view. Scale bars: 1 mm.

FIGURE 1 in Comparative morphology and taxonomy of the tiger moth genus Epanycles Butler (Lepidoptera, Erebidae, Arctiinae, Arctiini, Ctenuchina), with notes on related genera

FIGURE 1. Habitus of the species treated herein. A) Epanycles imperialis from Taperinha, Pará, Brazil (MZSP); B) Hyaleucerea gigantea from San Pedro, Cosñipata Valley, Cuzco, Peru (MZSP); C) Hyaleucerea erythrotela from Fazenda Taperinha, Santarém, Pará, Brazil (MZSP); D) Eucereon obscurum from Serra do Navio, Amapá, Brazil (MNRJ); E) Eucereon archias from Paramaribo, Suriname (NHMUK); F) Sciopsyche tropica from Angra dos Reis, Rio de Janeiro, Brazil (MZSP); G) Episcepsis endodasia from Boracéia, São Paulo, Brazil (MZSP); H) Episcepsis luctuosa, Suriname; I) Syntype of Episcepsis satania, Santa Rosa, Mexico.

FIGURE 4 in Comparative morphology and taxonomy of the tiger moth genus Epanycles Butler (Lepidoptera, Erebidae, Arctiinae, Arctiini, Ctenuchina), with notes on related genera

FIGURE 4. Male genitalia of Eucereon obscurum. A) Male genitalia, dorsal view; B) Same, lateral view; C) Aedeagus. Scale bars: 1 mm.

FIGURE 4 in Comparative seed morphology of the Antillean genus Calycogonium (Melastomataceae: Miconieae) as a source of characters to untangle its complex taxonomy

FIGURE 4. Seeds of Calycogonium apleurum, Calycogonium grisebachii, and Tetrazygia brachycentra. A–B. Calycogonium apleurum. C–D. Calycogonium grisebachii. E–F. Tetrazygia brachycentra. (scale bars A, C, E=100 µm; B=200 µm; D, F=10 µm; for voucher information see appendix 1).

FIGURE 3. Seed Types III–V.Type III.A–B. Calycogonium angulatum.C–D. Calycogonium domatiatum.Type IV in Comparative seed morphology of the Antillean genus Calycogonium (Melastomataceae: Miconieae) as a source of characters to untangle its complex taxonomy

FIGURE 3. Seed Types III–V.Type III.A–B. Calycogonium angulatum.C–D. Calycogonium domatiatum.Type IV: E. Calycogonium saxicola. F. Tetrazygia lanceolata. G. Tetrazygia eleagnoides. H. Tetrazygia bicolor. Type V: I. Calycogonium pseudofloribundum. J. Calycogonium revolutum. K. Pachyanthus discolor, detail of testa. L. Calycogonium cocoense detail of testa. (scale bars A, C, E–G, =100 µm; I–J, =500 µm; B, D, K–L=10 µm; for voucher information see appendix 1).

FIGURE 2 in Comparative seed morphology of the Antillean genus Calycogonium (Melastomataceae: Miconieae) as a source of characters to untangle its complex taxonomy

FIGURE 2. Seed Types IIa, IIb, III. Type IIa:A–B. Miconia baracoensis. C. Pachyanthus monocephalus. D. Calycogonium clidemiodes. Type IIb: E–G. Miconia uninervis. Type III: H.Calycogonium glabratum. I. Miconia moensis. J. Pachyanthus pedicellatus. K–L. Calycogonium rhamnoideum. (scale bars A, C–F, =500 µm; H–K= 100 µm; B,G, L=10 µm; for voucher information see appendix 1).

FIGURE 1 in Comparative seed morphology of the Antillean genus Calycogonium (Melastomataceae: Miconieae) as a source of characters to untangle its complex taxonomy

FIGURE 1. Seed Types Ia, Ib.Type Ia: A. Calycogonium reticulatum. B. Clidemia cf. wrightii. C. Clidemia cf. barbeyana. D. Calycogonium heterophyllum, detail of testa. Type Ib: E. Calycogonium hispidulum. F–G. Calycogonium tetragonolobum. (scale bars A–C, E–G=100 µm; D=20 µm; for voucher information see appendix 1).

FIGURE 21. Maximum parsimony 16S rRNA phylogram for the Boophis albipunctatus group. From 485 total characters, 391 were constant and 72 in Integrative taxonomy of Malagasy treefrogs: combination of molecular genetics, bioacoustics and comparative morphology reveals twelve additional species of Boophis 2383

FIGURE 21. Maximum parsimony 16S rRNA phylogram for the Boophis albipunctatus group. From 485 total characters, 391 were constant and 72 parsimony informative. MP searches retained 26 trees of which a strict consensus is shown. Consensus support values higher than 50, from 2000 bootstrap replicates, are shown; an asterisk indicates Bayesian posterior probabilities equal or higher than 95%. Species newly described herein are in bold.

FIGURE 27 in Integrative taxonomy of Malagasy treefrogs: combination of molecular genetics, bioacoustics and comparative morphology reveals twelve additional species of Boophis 2383

FIGURE 27. Spectrogram and waveform of call type 1 of Boophis luciae sp. nov. from Andasibe (recorded on 1 February 1995, air temperature 22°C).

FIGURE 19 in Integrative taxonomy of Malagasy treefrogs: combination of molecular genetics, bioacoustics and comparative morphology reveals twelve additional species of Boophis 2383

FIGURE 19. (A) Male holotype of Boophis sandrae sp. nov. (ZMA 20133) from Ranomafana; (B) female paratype of Boophis sandrae sp. nov. (ZSM 236/2006) from Ambatolahy.

FIGURE 10 in Integrative taxonomy of Malagasy treefrogs: combination of molecular genetics, bioacoustics and comparative morphology reveals twelve additional species of Boophis 2383

FIGURE 10. Male holotype of Boophis entingae sp. nov. (ZSM 2083/2007): (A) dorsolateral view; (B) ventral view; (C) detail showing colouration of posterior surfaces of thigh.

FIGURE 8 in Integrative taxonomy of Malagasy treefrogs: combination of molecular genetics, bioacoustics and comparative morphology reveals twelve additional species of Boophis 2383

FIGURE 8. Male of Boophis brachychir (ZSM 2157/2007) from Forêt d'Ambre Special Reserve: (A) dorsolateral view; (B) ventral view.

FIGURE 5 in Integrative taxonomy of Malagasy treefrogs: combination of molecular genetics, bioacoustics and comparative morphology reveals twelve additional species of Boophis 2383

FIGURE 5. Spectrograms and waveforms of advertisement calls of: (A) Boophis andrangoloaka from Ambohitantely Special Reserve (recorded on 18 January 2005, air temperature app. 18°C); (B) Boophis rhodoscelis from Ranomafanakely, Ranomafana National Park (recorded on 28 January 2004, air temperature app. 21°C).

FIGURE 9 in Integrative taxonomy of Malagasy treefrogs: combination of molecular genetics, bioacoustics and comparative morphology reveals twelve additional species of Boophis 2383

FIGURE 9. Spectrogram, corresponding waveform and expanded waveform of the advertisement call of Boophis brachychir from Manongarivo Special Reserve (recorded on 1 February 2003, air temperature 24.5°C).

FIGURE 7. Maximum parsimony 16S in Integrative taxonomy of Malagasy treefrogs: combination of molecular genetics, bioacoustics and comparative morphology reveals twelve additional species of Boophis 2383

FIGURE 7. Maximum parsimony 16S rRNA phylogram of species of the Boophis goudoti group. From 510 total characters, 340 were constant and 130 parsimony informative. MP searches retained 3681 trees of which a strict consensus is shown. Consensus support values higher than 50, from 2000 bootstrap replicates, are shown; an asterisk indicates Bayesian posterior probabilities equal or higher than 95%. Species newly described or resurrected herein are in bold.

FIGURE 25 in Integrative taxonomy of Malagasy treefrogs: combination of molecular genetics, bioacoustics and comparative morphology reveals twelve additional species of Boophis 2383

FIGURE 25. Comparative waveform sections (each 2000 ms duration) of advertisement calls of species in the Boophis albipunctatus group: (A) Boophis schuboeae (Ranomafana National Park, 23°C); (B) Boophis haingana sp. nov. (Andohahela National Park, low altitude, 23.2°C); (C) Boophis haingana sp. nov. (Andohahela National Park, 1600 m a.s.l., 17.6°C); (D) Boophis ankaratra (Manjakatompo, 18°C); (E) Boophis miadana sp. nov. (Andohahela National Park, 1550 m a.s.l., 17.6°C).