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FIGURE 6 in Two new Bent-toed Geckos of the Cyrtodactylus pulchellus complex from Peninsular Malaysia and multiple instances of convergent adaptation to limestone forest ecosystems

FIGURE 6. Cyrtodactylus lenggongensis sp. nov. from Lenggong Valley, Perak, Peninsular Malaysia. Upper left: male holotype LSUHC 9974. Upper right: juvenile male paratype LSUHC 9976. Lower: type series from left to right; male holotype LSUHC 9974, female paratype LUSHC 9975, male paratype LSUHC 9976, and juvenile female paratype LSUHC 9977.

FIGURE 5 in Two new Bent-toed Geckos of the Cyrtodactylus pulchellus complex from Peninsular Malaysia and multiple instances of convergent adaptation to limestone forest ecosystems

FIGURE 5. Left: limestone forest habitat and karst tower of the type locality of Cyrtodactylus hidupselamanya sp. nov. from Felda Chiku 7, Kelantan, Peninsular Malaysia. Right: Three dimensional Google Earth satellite image view of the karst formation encompassing the type locality illustrating its island-like nature being that it is surrounded by oil palm agriculture. White circles denote approximate collecting sites of the type series. Bottom: edge of the karst tower at the type locality.

FIGURE 4 in Two new Bent-toed Geckos of the Cyrtodactylus pulchellus complex from Peninsular Malaysia and multiple instances of convergent adaptation to limestone forest ecosystems

FIGURE 4. Type series of Cyrtodactylus hidupselamanya sp. nov. from Felda Chiku 7, Kelantan, Peninsular Malaysia. Voucher numbers are in the LSUHC series. LSUHC 12163 is the holotype.

FIGURE 3 in Two new Bent-toed Geckos of the Cyrtodactylus pulchellus complex from Peninsular Malaysia and multiple instances of convergent adaptation to limestone forest ecosystems

FIGURE 3. Cyrtodactylus hidupselamanya sp. nov. from Felda Chiku 7, Kelantan, Peninsular Malaysia. Upper left: male paratype LSUHC12175. Upper right: female paratype LSUHC 12173. Lower left: hatchling paratype LSUHC 12177. Lower right: juvenile paratype LSUHC 12176.

FIGURE 2 in Two new Bent-toed Geckos of the Cyrtodactylus pulchellus complex from Peninsular Malaysia and multiple instances of convergent adaptation to limestone forest ecosystems

FIGURE 2. BEAST chronogram of the Cyrtodactylus pulchellus complex. Black dots represent nodes supported by PP of 0.95 and UFboot of 95 and above. Gray dots are nodes having only UFboot of 95 and above. Red branches framed by dates in mya delimit the time frames within which transformations from granite forest ancestors gave rise to karst ecosystem ancestors. Red circles delimit the most inclusive descendent lineages of those transformations.

FIGURE 1 in Two new Bent-toed Geckos of the Cyrtodactylus pulchellus complex from Peninsular Malaysia and multiple instances of convergent adaptation to limestone forest ecosystems

FIGURE 1. Distribution of the species of the Cyrtodactylus pulchellus complex from the Thai-Malay Peninsula. Enclosed stars represent type localities of the newly described species.

opennotspecifiedDec 2010View details →

FIGURES 1–8 in A new species of genus Thrips (Thysanoptera, Thripinae) from flowers in Peninsular Malaysia

FIGURES 1–8. Thrips razanii sp. n.. (1) Head, dorsal; (2) Pronotum; (3) Antenna; (4) Female; (5) Meso- and metanotum; (6) Male abdominal sternites; (7) Female abdominal tergite VII–VIII; (8) Forewing.

FIGURE 1 in A new, diminutive, upland Sphenomorphus Fitzinger 1843 (Squamata: Scincidae) from the Belum-Temengor Forest Complex, Peninsular Malaysia

FIGURE 1. Distribution of the diminutive, montane and insular, endemic species of Sphenomorphus in Peninsular Malaysia. 1 = Royal Belum State Park, Perak; 2 = Temengor Forest Reserve, Perak; 3 = head waters of the Pelus River, Perak.

FIGURE 3 in A new, diminutive, upland Sphenomorphus Fitzinger 1843 (Squamata: Scincidae) from the Belum-Temengor Forest Complex, Peninsular Malaysia

FIGURE 3. Paratype of Sphenomorphus temengorensis (LSUHC 5650) from the Temengor Forest Reserve, Perak.

FIGURE 2 in A new, diminutive, upland Sphenomorphus Fitzinger 1843 (Squamata: Scincidae) from the Belum-Temengor Forest Complex, Peninsular Malaysia

FIGURE 2. Type series of Sphenomorphus temengorensis. Holotype DWNP 5018 (upper) and paratype LSUHC 5659 (lower).

FIGURES 25–28 in Species of the genus Thrips (Thysanoptera) from Peninsular Malaysia, with a checklist of recorded Thripidae

FIGURES 25–28. Sternites of Thrips species. (25) T. aspinus sternites V–VI; (26) T. parvispinus sternites VI–VII; (27) T. vitticornis sternites VI–VII; (28) T. hanifahi sternites VI–VII.

FIGURES 14–24 in Species of the genus Thrips (Thysanoptera) from Peninsular Malaysia, with a checklist of recorded Thripidae

FIGURES 14–24. Thrips species. (14) T. simplex meso and metanotum; (15) T. parvispinus meso and metanotum; (16) T. vitticornis meso and metanotum; (17) T. florum forewing clavus; (18) T. hawaiiensis forewing clavus; (19) T. hanifahi head; (20) T. flavus head; (21) T. hanifahi pronotum; (22) T. coloratus tergites VII–VIII; (23) T. leeuwenii tergites VII–VIII; (24) T. hanifahi tergites VII–X.

Figure 3 in Repeated evolution of sympatric, palaeoendemic species in closely related, co-distributed lineages of Hemiphyllodactylus Bleeker, 1860 (Squamata: Gekkonidae) across a sky-island archipelago in Peninsular Malaysia

Figure 3. Habitat at the type locality of Hemiphyllodactylus bintik sp. nov., Gunung Tebu, Terenganu, Peninsular Malaysia.

Figure 4 in Repeated evolution of sympatric, palaeoendemic species in closely related, co-distributed lineages of Hemiphyllodactylus Bleeker, 1860 (Squamata: Gekkonidae) across a sky-island archipelago in Peninsular Malaysia

Figure 4. The results of the different partitioning schemes on node age estimates. When applicable, node age estimates from Heinicke et al. (2011) for nuclear DNA (nDNA) only and combined mitochondrial (mtDNA) and nDNA were includ- ed for comparative purposes.

Figure 2 in Repeated evolution of sympatric, palaeoendemic species in closely related, co-distributed lineages of Hemiphyllodactylus Bleeker, 1860 (Squamata: Gekkonidae) across a sky-island archipelago in Peninsular Malaysia

Figure 2. Dorsal and ventral view of the holotype of Hemiphyllodactylus bintik sp. nov. (LSUHC 11216).

Figure 1. A, Bayesian time tree for Hemiphyllodactylus with 95 in Repeated evolution of sympatric, palaeoendemic species in closely related, co-distributed lineages of Hemiphyllodactylus Bleeker, 1860 (Squamata: Gekkonidae) across a sky-island archipelago in Peninsular Malaysia

Figure 1. A, Bayesian time tree for Hemiphyllodactylus with 95% highest posterior density (95% HPD) intervals for major nodes represented by purple bars. Black circles at nodes are posterior probabilities ≥ 0.95; grey circles at nodes are posterior probabilities <0.95. B, Bayesian time tree for the Hemiphyllodactylus harterti group. C, Distribution of the H. harterti group in Peninsular Malaysia.

Subspecies and Distribution. H. u. wrva Hodgson, 1836 — Nepal through Indochina to Peninsular Malaysia. H. u. annamensis Bechthold, 1936 — Vietnam. H. u. formosanus Bechthold, 1936 — Taiwart. H. u. sinensis Bechthold, 1936 — S China (and Hainan I). in Herpestidae

Subspecies and Distribution. H. u. wrva Hodgson, 1836 — Nepal through Indochina to Peninsular Malaysia. H. u. annamensis Bechthold, 1936 — Vietnam. H. u. formosanus Bechthold, 1936 — Taiwart. H. u. sinensis Bechthold, 1936 — S China (and Hainan I).

Distribution. Mainland SE Asia, Peninsular Malaysia, and Sumatra. The Javan Mongoose or the Small Indian Mongoose is said to occur on Hong Kong (since the 1980s), and to have been introduced to some Indonesian islands. in Herpestidae

Distribution. Mainland SE Asia, Peninsular Malaysia, and Sumatra. The Javan Mongoose or the Small Indian Mongoose is said to occur on Hong Kong (since the 1980s), and to have been introduced to some Indonesian islands.

Subspecies and Distribution. H. e. edwardsii Geoffroy Saint-Hilaire, 1818 — SE India and Sri Lanka. H. e. carnaticus Wroughton, 1921 — SW India (Karnatka). H. e. moerens Wroughton, 1915 — Bangladesh, Bhutan, C & NE India, and Nepal. H. e. montanus Bechthold, 1936 — Saudi Arabia to NW India. H. e. pallens Ryley, 1914 — W India (Gujarat). A few old museum specimens are reported from Peninsular Malaysia, whereit is said to have been introduced, butit has not been recorded there since the beginning of the 20" century. in Herpestidae

Subspecies and Distribution. H. e. edwardsii Geoffroy Saint-Hilaire, 1818 — SE India and Sri Lanka. H. e. carnaticus Wroughton, 1921 — SW India (Karnatka). H. e. moerens Wroughton, 1915 — Bangladesh, Bhutan, C & NE India, and Nepal. H. e. montanus Bechthold, 1936 — Saudi Arabia to NW India. H. e. pallens Ryley, 1914 — W India (Gujarat). A few old museum specimens are reported from Peninsular Malaysia, whereit is said to have been introduced, butit has not been recorded there since the beginning of the 20" century.

Subspecies and Distribution. H. b. brachyurus Gray, 1837 — S Thailand, Peninsular Malaysia, and Singapore. H. b. palawanusJ. A. Allen, 1910 — the Philippines (Palawan & Calamian Is). H. b. rajah Thomas, 1921 — Borneo. H. b. sumatrius Thomas, 1921 — Sumatra. in Herpestidae

Subspecies and Distribution. H. b. brachyurus Gray, 1837 — S Thailand, Peninsular Malaysia, and Singapore. H. b. palawanusJ. A. Allen, 1910 — the Philippines (Palawan & Calamian Is). H. b. rajah Thomas, 1921 — Borneo. H. b. sumatrius Thomas, 1921 — Sumatra.