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Copyright: © 2011 Janzen and Bopage. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, Amphibian & Reptile Conservation 5(2):1-13. provided the original author and source are credited. The herpetofauna of a small and unprotected patch of tropical rainforest in Morningside, Sri Lanka 1,3PETER JANZEN AND 2MALAKA BOPAGE 1Rheinallee 13, 47119 Duisburg, GERMANY 2Biodiversity Education & Exploration Society (BEES) 63/c Wackvella road Galle 80000, SRI LANKA Abstract.—Morningside is an exceptional area in Sri Lanka with highly endemic herpetofauna. How- ever, this relictual forest area lies inside a tea plantation and is mostly lacking conservation protec- tion. Species inventories of remaining rainforest patches are currently incomplete, and information about the behavior and ecology of the herpetofauna of Morningside is poorly known. In our survey, we identified 13 amphibian species and recorded an additional two species that could not be identi- fied with existing keys. We determined 11 reptile species from this patch of forest, and another un- identifiedCnemaspis gecko was recorded. We did not assess the herpetofauna outside of this forest patch. Some species are described for the first time in Morningside, suggesting a wider distribution in Sri Lanka. We also document a call from a male Pseudophilautus cavirostris for the first time. Perspectives for future surveys are given. Key words. Survey, Morningside, Sri Lanka, herpetofauna, conservation, Pseudophilautus cavirostris Citation: Jansen, P. and Bopage, M. 2011. The herpetofauna of a small and unprotected patch of tropical rainforest in Morningside, Sri Lanka. -
Keanekaragaman Jenis Squamata Di Kawasan Wisata Air Terjun Roro Kuning Kecamatan Loceret Kabupaten Nganjuk the Diversity of Spec
Simki-Techsain Vol. 01 No. 01 Tahun 2017 ISSN : XXXX-XXXX KEANEKARAGAMAN JENIS SQUAMATA DI KAWASAN WISATA AIR TERJUN RORO KUNING KECAMATAN LOCERET KABUPATEN NGANJUK THE DIVERSITY OF SPECIES SQUAMATA IN THE TOURIST AREA WATERFALL RORO KUNING KECAMATAN LOCERET KABUPATEN NGANJUK Oleh: SEPTI WULANDARI 13.1.01.06.0034 Dibimbing oleh : Dr. Sulistiono, M.Si. Tisa Rizkika N. A., S.Pd., M.Sc. PROGRAM STUDI PENDIDIKAN BIOLOGI FAKULTAS KEGURUAN DAN ILMU PENDIDIKAN (FKIP) UNIVERSITAS NUSANTARA PGRI KEDIRI 2017 Simki-Techsain Vol. 01 No. 01 Tahun 2017 ISSN : XXXX-XXXX Artikel Skripsi Universitas Nusantara PGRI Kediri SURAT PERNYATAAN ARTIKEL SKRIPSI TAHUN 2017 Yang bertanda tangan di bawah ini: Nama Lengkap :Septi Wulandari NPM :13.1.01.06.0034 Telepun/HP :0857 8529 3572 Alamat Surel (Email) :[email protected] Judul Artikel :Keanekaragaman Jenis Squamata di Kawasan Wisata Air Terjun Roro Kuning Kecamatan Loceret Kabupaten Nganjuk Fakultas – Program Studi :FKIP-Pendidikan Biologi Nama Perguruan Tinggi :Universitas Nusantara PGRI Kediri Alamat Perguruan Tinggi :Jl. KH. Achmad DahlanNo. 76, Mojoroto, Kota Kediri Dengan ini menyatakan bahwa : a. artikel yang saya tulis merupakan karya saya pribadi (bersama tim penulis) dan bebas plagiarisme; b. artikel telah diteliti dan disetujui untuk diterbitkan oleh Dosen Pembimbing I dan II. Demikian surat pernyataan ini saya buat dengan sesungguhnya. Apabila di kemudian hari ditemukan ketidaksesuaian data dengan pernyataan ini dan atau ada tuntutan dari pihak lain, saya bersedia bertanggungjawab dan diproses sesuai dengan ketentuan yang berlaku. Mengetahui Kediri, 7 Agustus 2017 Pembimbing I Pembimbing II Penulis Dr. Sulistiono, M.Si. Tisa Rizkika N. A., S.Pd., M.Sc. Septi Wulandari NIDN. -
On the Andaman and Nicobar Islands, Bay of Bengal
Herpetology Notes, volume 13: 631-637 (2020) (published online on 05 August 2020) An update to species distribution records of geckos (Reptilia: Squamata: Gekkonidae) on the Andaman and Nicobar Islands, Bay of Bengal Ashwini V. Mohan1,2,* The Andaman and Nicobar Islands are rifted arc-raft of 2004, and human-mediated transport can introduce continental islands (Ali, 2018). Andaman and Nicobar additional species to these islands (Chandramouli, 2015). Islands together form the largest archipelago in the In this study, I provide an update for the occurrence Bay of Bengal and a high proportion of terrestrial and distribution of species in the family Gekkonidae herpetofauna on these islands are endemic (Das, 1999). (geckos) on the Andaman and Nicobar Islands. Although often lumped together, the Andamans and Nicobars are distinct from each other in their floral Materials and Methods and faunal species communities and are geographically Teams consisted of between 2–4 members and we separated by the 10° Channel. Several studies have conducted opportunistic visual encounter surveys in shed light on distribution, density and taxonomic accessible forested and human-modified areas, both aspects of terrestrial herpetofauna on these islands during daylight hours and post-sunset. These surveys (e.g., Das, 1999; Chandramouli, 2016; Harikrishnan were carried out specifically for geckos between and Vasudevan, 2018), assessed genetic diversity November 2016 and May 2017, this period overlapped across island populations (Mohan et al., 2018), studied with the north-east monsoon and summer seasons in the impacts of introduced species on herpetofauna these islands. A total of 16 islands in the Andaman and and biodiversity (e.g., Mohanty et al., 2016a, 2019), Nicobar archipelagos (Fig. -
Squamate Reptiles Challenge Paradigms of Genomic Repeat Element Evolution Set by Birds and Mammals
ARTICLE DOI: 10.1038/s41467-018-05279-1 OPEN Squamate reptiles challenge paradigms of genomic repeat element evolution set by birds and mammals Giulia I.M. Pasquesi1, Richard H. Adams1, Daren C. Card 1, Drew R. Schield1, Andrew B. Corbin1, Blair W. Perry1, Jacobo Reyes-Velasco1,2, Robert P. Ruggiero2, Michael W. Vandewege3, Jonathan A. Shortt4 & Todd A. Castoe1 1234567890():,; Broad paradigms of vertebrate genomic repeat element evolution have been largely shaped by analyses of mammalian and avian genomes. Here, based on analyses of genomes sequenced from over 60 squamate reptiles (lizards and snakes), we show that patterns of genomic repeat landscape evolution in squamates challenge such paradigms. Despite low variance in genome size, squamate genomes exhibit surprisingly high variation among spe- cies in abundance (ca. 25–73% of the genome) and composition of identifiable repeat ele- ments. We also demonstrate that snake genomes have experienced microsatellite seeding by transposable elements at a scale unparalleled among eukaryotes, leading to some snake genomes containing the highest microsatellite content of any known eukaryote. Our analyses of transposable element evolution across squamates also suggest that lineage-specific var- iation in mechanisms of transposable element activity and silencing, rather than variation in species-specific demography, may play a dominant role in driving variation in repeat element landscapes across squamate phylogeny. 1 Department of Biology, University of Texas at Arlington, 501S. Nedderman Drive, Arlington, TX 76019, USA. 2 Department of Biology, New York University Abu Dhabi, Saadiyat Island, United Arab Emirates. 3 Department of Biology, Institute for Genomics and Evolutionary Medicine, Temple University, Philadelphia, PA 19122, USA. -
Potential Risks of Plant Invasions in Protected Areas of Sri Lanka Under Climate Change with Special Reference to Threatened Vertebrates
Electronic Supplementary Materials Journal: Climate Potential Risks of Plant Invasions in Protected Areas of Sri Lanka under Climate Change with Special Reference to Threatened Vertebrates Champika Kariyawasam1,2,*, Lalit Kumar1 and Sujith Ratnayake1,2 Table S1. Fourteen priority IAPS used for MaxEnt model run (adapted from MMD&E [1]). NP = national park; SNR = strict nature reserve. Life form Affected climatic Referen Species Common (Year of Mechanism Impact zones (Protected ce (Family) name introductio areas) n) Reduce native Wet zone Alstonia Compete for Hard Tree species (Peak Wilderness macrophylla resources [2] milkwood (unknown) regeneration sanctuary, Sinharaja (Apocynaceae) and Hantana forests) Grow rapidly and Convert wetlands Wet zone Annona glabra Pond Tree produce high into terrestrial (Muthurajawela [3-4] (Annonaceae) apple (unknown) biomass ecosystems wetland sanctuary) Montane zone (Knuckles forest, Austroeupatoriu Inhibit natural Austroeup Shrub Exclude native Horton Plains NP, m inulifolium succession by native [5] atorium (unknown) woody species Peak wilderness (Asteraceae) species sanctuary, Hakgala SNR) Clidemia hirta Soapbush, Compete with Alter forest Wet zone (Melastomatace Koster's Herb (1894) native species in [6] regeneration (Sinharaja forest) ae) curse gaps Dillenia Alter soil physical Impact nutrient Shrubby Tree Lowland wet zone suffruticosa and chemical absorption of [7] Dillenia (1882) (Sinharaja forest) (Dilleniaceae) properties native plants Suppress undergrowth plant Shade out native species plants -
Dr. Kalana CV
Maduwage Kalana Prasad University Lecturer / Professor in Biochemistry / Biomedical Researcher http://med.pdn.ac.lk/departments/biochemistry/staff/kalana.html https://scholar.google.com/citations?user=lf3F3OsAAAAJ&hl=en https://www.researchgate.net/proile/Kalana_Maduwage Google Scholar citations: 764, h-index 17 (April 2019) E.mail: [email protected] Date of birth: 5 November 1980 Residence: 55A Galkanda Road, Aniwatta, Kandy, 20000, Sri Lanka Contact: +94 7 1414 5738 Skype: kalanamaduwage Summary I have a Ph.D. in Clinical Pharmacology from the University of Newcastle, Australia, and am now working as a professor at department of Biochemistry, Faculty of Medicine, University of Peradeniya, Sri Lanka. I teach both undergraduate and postgraduate medical students in addition to preparing relevant teaching / learning material. In addition to being the founder- coordinator and chief examiner for the Integrated Human Biology modules of our M.B.,B.S. programme, I have nine years of experience in medical teaching, including three years’ teaching experience in the School of Medicine and Public Health of the University of Newcastle, Australia. My Ph.D. dissertation was on the coagulant effects of Sri Lankan snake venoms and the eficacy of antivenoms. This built on my M.Phil. programme (‘Systematics, venom characteristics and clinical features following envenomation by Sri Lankan hump-nosed vipers’) and M.B.,B.S at the University of Peradeniya. I have forty-two publications in SCI journals, 12 of these as irst author, and have won six international awards for research and thirteen national awards for research. I am focused and hardworking, and am familiar with clinical, pathophysiological and treatment aspects of snake envenomation. -
NHBSS 061 1G Hikida Fieldg
Book Review N$7+IST. BULL. S,$0 SOC. 61(1): 41–51, 2015 A Field Guide to the Reptiles of Thailand by Tanya Chan-ard, John W. K. Parr and Jarujin Nabhitabhata. Oxford University Press, New York, 2015. 344 pp. paper. ISBN: 9780199736492. 7KDLUHSWLOHVZHUHÀUVWH[WHQVLYHO\VWXGLHGE\WZRJUHDWKHUSHWRORJLVWV0DOFROP$UWKXU 6PLWKDQG(GZDUG+DUULVRQ7D\ORU7KHLUFRQWULEXWLRQVZHUHSXEOLVKHGDV6MITH (1931, 1935, 1943) and TAYLOR 5HFHQWO\RWKHUERRNVDERXWUHSWLOHVDQGDPSKLELDQV LQ7KDLODQGZHUHSXEOLVKHG HJ&HAN-ARD ET AL., 1999: COX ET AL DVZHOODVPDQ\ SDSHUV+RZHYHUWKHVHERRNVZHUHWD[RQRPLFVWXGLHVDQGQRWJXLGHVIRURUGLQDU\SHRSOH7ZR DGGLWLRQDOÀHOGJXLGHERRNVRQUHSWLOHVRUDPSKLELDQVDQGUHSWLOHVKDYHDOVREHHQSXEOLVKHG 0ANTHEY & GROSSMANN, 1997; DAS EXWWKHVHERRNVFRYHURQO\DSDUWRIWKHIDXQD The book under review is very well prepared and will help us know Thai reptiles better. 2QHRIWKHDXWKRUV-DUXMLQ1DEKLWDEKDWDZDVP\ROGIULHQGIRUPHUO\WKH'LUHFWRURI1DWXUDO +LVWRU\0XVHXPWKH1DWLRQDO6FLHQFH0XVHXP7KDLODQG+HZDVDQH[FHOOHQWQDWXUDOLVW DQGKDGH[WHQVLYHNQRZOHGJHDERXW7KDLDQLPDOVHVSHFLDOO\DPSKLELDQVDQGUHSWLOHV,Q ZHYLVLWHG.KDR6RL'DR:LOGOLIH6DQFWXDU\WRVXUYH\KHUSHWRIDXQD+HDGYLVHGXV WRGLJTXLFNO\DURXQGWKHUH:HFROOHFWHGIRXUVSHFLPHQVRIDibamusZKLFKZHGHVFULEHG DVDQHZVSHFLHVDibamus somsaki +ONDA ET AL 1RZ,DPYHU\JODGWRNQRZWKDW WKLVERRNZDVSXEOLVKHGE\KLPDQGKLVFROOHDJXHV8QIRUWXQDWHO\KHSDVVHGDZD\LQ +LVXQWLPHO\GHDWKPD\KDYHGHOD\HGWKHSXEOLFDWLRQRIWKLVERRN7KHERRNLQFOXGHVQHDUO\ DOOQDWLYHUHSWLOHV PRUHWKDQVSHFLHV LQ7KDLODQGDQGPRVWSLFWXUHVZHUHGUDZQZLWK H[FHOOHQWGHWDLO,WLVDYHU\JRRGÀHOGJXLGHIRULGHQWLÀFDWLRQRI7KDLUHSWLOHVIRUVWXGHQWV -
Species Account
REPTILIA Order OPHIDIA (Snakes) I. Family COLUBRIDAE Ahaetulla prasina Green Vine Snake This snake was found in Renah Kayu Embun and Napal Licin survey sites at elevation 1400 meters asl and 300 meters asl respectively. Usually it can be seen in degraded habitat including plantation, secondary growth and house compounds, to primary rain forest (Inger and Stuebing, 2005; Kurniati, 2003). It occurs from lowlands up to mountain forests over 1500 meters asl (Kurniati et al., 2001; Kurniati, 2003). It is common species at low elevation (Inger and Stuebing, 2005), but become rare at high elevation such as Renah Kayu Embun survey site. This species is known from South-east Asia, East Indies (Sulawesi and The Lesser Sunda) (Stuebing and Inger, 1999: de Lang and Vogel, 2005). Figure 91. A. prasina (Photograph by H. Kurniati). Amphiesma sp This undescribed snake was found in Muara Labuh survey site at elevation 800 meters asl. It was a nocturnal snake that inhabited strong moving stream bank. The morphology of this snake is similar to A. kerinciense (David and Das, 2003). Possibly, it is a new species, but future study is needed. Figure 92. Amphiesma sp from Muara Labuh (Photograph by H. Kurniati). Aplopeltura boa Blunt-headed Tree Snake This snake was found in Upper Rupit River and Tapan survey sites at elevation 150 meters asl and 550 meters asl respectively. It inhabited lowland primary rain forest. It occurs at elevation between sea level to 1200 meters asl (Kurniati, 2003), but it is confined to be lowland. In Tapan survey site, it was rarely observed. -
Conservation Matters: CITES and New Herp Listings
Conservation matters:FEATURE | CITES CITES and new herp listings The red-tailed knobby newt (Tylototriton kweichowensis) now has a higher level of protection under CITES. Photo courtesy Milan Zygmunt/www. shutterstock.com What are the recent CITES listing changes and what do they mean for herp owners? Dr. Thomas E.J. Leuteritz from the U.S. Fish & Wildlife Service explains. id you know that your pet It is not just live herp may be a species of animals that are protected wildlife? Many covered by CITES, exotic reptiles and but parts and Damphibians are protected under derivatives too, such as crocodile skins CITES, also known as the Convention that feature in the on International Trade in Endangered leather trade. Plants Species of Wild Fauna and Flora. and timber are also Initiated in 1973, CITES is an included. international agreement currently Photo courtesy asharkyu/ signed by 182 countries and the www.shutterstock.com European Union (also known as responsibility of the Secretary of the How does CITES work? Parties), which regulates Interior, who has tasked the U.S. Fish Species protected by CITES are international trade in more than and Wildlife Service (USFWS) as the included in one of three lists, 35,000 wild animal and plant species, lead agency responsible for the referred to as Appendices, according including their parts, products, and Convention’s implementation. You to the degree of protection they derivatives. can help USFWS conserve these need: Appendix I includes species The aim of CITES is to ensure that species by complying with CITES threatened with extinction and international trade in specimens of and other wildlife laws to ensure provides the greatest level of wild animals and plants does not that your activities as a pet owner or protection, including restrictions on threaten their survival in the wild. -
Deep‐Time Convergent Evolution in Animal Communication Presented
Received: 18 November 2020 | Revised: 15 April 2021 | Accepted: 19 April 2021 DOI: 10.1111/ele.13773 LETTER Deep- time convergent evolution in animal communication presented by shared adaptations for coping with noise in lizards and other animals Terry J. Ord1 | Danielle A. Klomp1 | Thomas C. Summers1 | Arvin Diesmos2 | Norhayati Ahmad3 | Indraneil Das4 1Evolution & Ecology Research Centre Abstract and the School of Biological, Earth and Environmental Sciences, University of New Convergence in communication appears rare compared with other forms of ad- South Wales, Sydney, NSW, Australia aptation. This is puzzling, given communication is acutely dependent on the envi- 2Herpetology Section, Zoology Division, National Museum of the Philippines, ronment and expected to converge in form when animals communicate in similar Manila, Philippines habitats. We uncover deep- time convergence in territorial communication between 3Department of Biological Sciences and Biotechnology, Universiti Kebangsaan two groups of tropical lizards separated by over 140 million years of evolution: Malaysia, Bangi, Malaysia the Southeast Asian Draco and Caribbean Anolis. These groups have repeatedly 4Institute of Biodiversity and Environmental Conservation, Universiti converged in multiple aspects of display along common environmental gradients. Malaysia Sarawak, Kota Samarahan, Malaysia Robot playbacks to free- ranging lizards confirmed that the most prominent con- vergence in display is adaptive, as it improves signal detection. We then provide Correspondence Terry J. Ord, Evolution & Ecology evidence from a sample of the literature to further show that convergent adap- Research Centre and the School of Biological, Earth and Environmental tation among highly divergent animal groups is almost certainly widespread in Sciences, University of New South Wales, nature. -
Vol. 25 No. 1 March, 2000 H a M a D R Y a D V O L 25
NO.1 25 M M A A H D A H O V D A Y C R R L 0 0 0 2 VOL. 25NO.1 MARCH, 2000 2% 3% 2% 3% 2% 3% 2% 3% 2% 3% 2% 3% 2% 3% 2% 3% 2% 3% 4% 5% 4% 5% 4% 5% 4% 5% 4% 5% 4% 5% 4% 5% 4% 5% 4% 5% HAMADRYAD Vol. 25. No. 1. March 2000 Date of issue: 31 March 2000 ISSN 0972-205X Contents A. E. GREER & D. G. BROADLEY. Six characters of systematic importance in the scincid lizard genus Mabuya .............................. 1–12 U. MANTHEY & W. DENZER. Description of a new genus, Hypsicalotes gen. nov. (Sauria: Agamidae) from Mt. Kinabalu, North Borneo, with remarks on the generic identity of Gonocephalus schultzewestrumi Urban, 1999 ................13–20 K. VASUDEVAN & S. K. DUTTA. A new species of Rhacophorus (Anura: Rhacophoridae) from the Western Ghats, India .................21–28 O. S. G. PAUWELS, V. WALLACH, O.-A. LAOHAWAT, C. CHIMSUNCHART, P. DAVID & M. J. COX. Ethnozoology of the “ngoo-how-pak-pet” (Serpentes: Typhlopidae) in southern peninsular Thailand ................29–37 S. K. DUTTA & P. RAY. Microhyla sholigari, a new species of microhylid frog (Anura: Microhylidae) from Karnataka, India ....................38–44 Notes R. VYAS. Notes on distribution and breeding ecology of Geckoella collegalensis (Beddome, 1870) ..................................... 45–46 A. M. BAUER. On the identity of Lacerta tjitja Ljungh 1804, a gecko from Java .....46–49 M. F. AHMED & S. K. DUTTA. First record of Polypedates taeniatus (Boulenger, 1906) from Assam, north-eastern India ...................49–50 N. M. ISHWAR. Melanobatrachus indicus Beddome, 1878, resighted at the Anaimalai Hills, southern India ............................. -
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HAMADRYAD Vol. 27. No. 2. August, 2003 Date of issue: 31 August, 2003 ISSN 0972-205X CONTENTS T. -M. LEONG,L.L.GRISMER &MUMPUNI. Preliminary checklists of the herpetofauna of the Anambas and Natuna Islands (South China Sea) ..................................................165–174 T.-M. LEONG & C-F. LIM. The tadpole of Rana miopus Boulenger, 1918 from Peninsular Malaysia ...............175–178 N. D. RATHNAYAKE,N.D.HERATH,K.K.HEWAMATHES &S.JAYALATH. The thermal behaviour, diurnal activity pattern and body temperature of Varanus salvator in central Sri Lanka .........................179–184 B. TRIPATHY,B.PANDAV &R.C.PANIGRAHY. Hatching success and orientation in Lepidochelys olivacea (Eschscholtz, 1829) at Rushikulya Rookery, Orissa, India ......................................185–192 L. QUYET &T.ZIEGLER. First record of the Chinese crocodile lizard from outside of China: report on a population of Shinisaurus crocodilurus Ahl, 1930 from north-eastern Vietnam ..................193–199 O. S. G. PAUWELS,V.MAMONEKENE,P.DUMONT,W.R.BRANCH,M.BURGER &S.LAVOUÉ. Diet records for Crocodylus cataphractus (Reptilia: Crocodylidae) at Lake Divangui, Ogooué-Maritime Province, south-western Gabon......................................................200–204 A. M. BAUER. On the status of the name Oligodon taeniolatus (Jerdon, 1853) and its long-ignored senior synonym and secondary homonym, Oligodon taeniolatus (Daudin, 1803) ........................205–213 W. P. MCCORD,O.S.G.PAUWELS,R.BOUR,F.CHÉROT,J.IVERSON,P.C.H.PRITCHARD,K.THIRAKHUPT, W. KITIMASAK &T.BUNDHITWONGRUT. Chitra burmanica sensu Jaruthanin, 2002 (Testudines: Trionychidae): an unavailable name ............................................................214–216 V. GIRI,A.M.BAUER &N.CHATURVEDI. Notes on the distribution, natural history and variation of Hemidactylus giganteus Stoliczka, 1871 ................................................217–221 V. WALLACH.