Cfreptiles & Amphibians

Total Page:16

File Type:pdf, Size:1020Kb

Cfreptiles & Amphibians WWW.IRCF.ORG TABLE OF CONTENTS IRCF REPTILES &IRCF AMPHIBIANS REPTILES • VOL &15, AMPHIBIANS NO 4 • DEC 2008 • 189 27(2):228–230 • AUG 2020 IRCF REPTILES & AMPHIBIANS CONSERVATION AND NATURAL HISTORY TABLE OF CONTENTS FEATURE ARTICLES . ChasingPredation Bullsnakes (Pituophis catenifer sayi )on in Wisconsin: an Egg Mass of the On the Road to Understanding the Ecology and Conservation of the Midwest’s Giant Serpent ...................... Joshua M. Kapfer 190 Terai. The Shared History Treefrog, of Treeboas (Corallus grenadensis) andPolypedates Humans on Grenada: taeniatus A Hypothetical Excursion ............................................................................................................................Robert W. Henderson 198 (Anura:RESEARCH Rhacophoridae), ARTICLES by Flesh Fly Larvae . The Texas Horned Lizard in Central and Western Texas ....................... Emily Henry, Jason Brewer, Krista Mougey, and Gad Perry 204 . The Knight Anole (Anolis equestris) in Florida .............................................(Diptera:Brian J. Camposano, Kenneth Sarcophagidae) L. Krysko, Kevin M. Enge, Ellen M. Donlan, and Michael Granatosky 212 CONSERVATION ALERT Bitupan Boruah and Abhijit Das . World’s Mammals in Crisis ............................................................................................................................................................. 220 . MoreWildlife Than Mammals Institute ............................................................................................................................... of India, Chandrabani, Dehradun, Uttarakhand-248001, India ([email protected])....................................... 223 . The “Dow Jones Index” of Biodiversity ........................................................................................................................................... 225 HUSBANDRY . Captive Care of the Central Netted Dragon ....................................................................................................... Shannon Plummer 226 he terrestrial eggs of anurans are vulnerable to attack an incidence of predation by dipteran larvae on an egg mass Tby predators suchPROFILE as fly larvae (Bokermann 1957; Villa of the Terai Treefrog (Polypedates taeniatus). 1977, 1980; Villa and. Kraig Townsend Adler: A Lifetime 1983; Promoting Davis Herpetology and ................................................................................................ Disney Among the foam nesting Michael L. rhacophorids,Treglia 234 Polypedates tae- 2003). Dipteran larvaeCOMMENTARY in the families Psychodidae (Villa niatus (Fig. 1) is restricted to the fragmented grassland patches 1980), Drosophilidae,. The EphydridaeTurtles Have Been Watching (Menin Me ........................................................................................................................ and Giaretta of India and Nepal (Anders Eric et Gangloff al. 1998;238 Ahmed and Dutta 2003), Phoridae (VoneshBOOK REVIEW 2000), Psychodidae, Syrphidae 2000; Schleich and Kästle 2002; Das et al. 2012). Deuti et al. (Villa et al. 1982; Davis. Threatened and Amphibians Disney of the 2003), World edited Tabanidae by S.N. Stuart, M. Hoffmann,(2018) J.S.recently Chanson, described N.A. Cox, acoustic behavior and larval devel- (Mohanty-Hejmadi andR. Dutta Berridge, P.1988), Ramani, andCalliphoridae B.E. Young .............................................................................................................. (Yorke opment of the species in West Robert Bengal. Powell 243 1983; Lin et al. 2000; Lue and Lin 2000; Karraker 2013), During August 2018, we observed a breeding congrega- CONSERVATION RESEARCH REPORTS: Summaries of Published Conservation Research Reports ................................. 245 and Sarcophagidae (FiladelfoNATURAL HISTORYet al. 2013) RESEARCH are known REPORTS to: Summariesfeed of Publishedtion of Reports P. taeniatus on Natural History in a................................. patch of Narrowleaf 247 Cattail (Typha on anuran eggs. However, NEWBRIEFS to the ............................................................................................................................... best of our knowledge, the angustifolia) at .......................................................Bidurkuti (29.28301ºN, 248 78.10165ºE; 208 m EDITORIAL INFORMATION ..................................................................................................................................................... 251 only report of predation FOCUS on ON egg CONSERVATION masses of Indian: A Project anurans You Can Supportis ...............................................................................................asl), Bijnor District, Uttar Pradesh, 252India. Males perched at by Mohanty-Hejmadi and Dutta (1988). Herein we report heights ranging from the ground to approximately 1.5 m and Front Cover. Shannon Plummer. Back Cover. Michael Kern Totat et velleseque audant mo Totat et velleseque audant mo estibus inveliquo velique rerchil estibus inveliquo velique rerchil erspienimus, quos accullabo. Ilibus erspienimus, quos accullabo. Ilibus aut dolor apicto invere pe dolum aut dolor apicto invere pe dolum fugiatis maionsequat eumque fugiatis maionsequat eumque moditia erere nonsedis ma sectiatur moditia erere nonsedis ma sectia- ma derrovitae voluptam, as quos tur ma derrovitae voluptam, as accullabo. Fig. 1. Terai Treefrogs (Polypedates taeniatus): Calling male on a perch (A) and an amplecting pair constructing a foam nest on the ground (B). Photographs by Bitupan Boruah. Copyright © 2020. Bitupan Boruah. All rights reserved. 228 IRCF Reptiles & Amphibians ISSN 1098-6324 BORUAH AND DAS IRCF REPTILES & AMPHIBIANS • 27(2):228–230 • AUG 2020 Acknowledgements We are thankful to the National Mission for Clean Ganga (NMCG), Government of India, for financial support; the Director and Dean, Wildlife Institute of India, Dehradun, for constant support; and the Forest Department of Uttar Pradesh for permission to carry out this study. We thank Arkojyoti Sarkar for help during fieldwork. Literature Cited Ahmed, M.F. and S.K. Dutta. 2000. First record of Polypedates taeniatus (Boulenger, 1906) from Assam, north-eastern India. Hamadryad 25: 49–50. Anders, C.C., A. Deiner, and H.H. Schleich. 1998. First record of Polypedates tae- niatus (Boulenger 1906) from Nepal (Amphibia, Anura: Rhacophoridae), pp. 73–86. In: H.H. Schleich, and W. Kastle (eds.), Contribution to the Herpetology of South Asia (Nepal, India). Veroff Fuhlrott Museum, Wuppertal, Germany. Bokermann, W.C. 1957. Frog eggs parasitized by dipterous larvae. Herpetologica 13: 231–232. da Silva, I.C.O., S.S. de Carvalho, K. Ceron, D.J. Santana, and L.E.R. Tavares. Fig. 2. Ventral (A) and lateral (B) views of flesh fly larvae (Diptera: 2019. A case of dipteran parasitism in Trachycephalus typhonius (Anura: Sarcophagidae) that had been feeding on the eggs of Terai Treefrogs Hylidae), with a summary of myiasis parasitism in anurans. Phyllomedusa 18: (Polypedates taeniatus). Scale bars = 1 mm. Photographs by Abhijit Das. 283–292. Das, A., D. Basu, L. Converse, and S.R.C. Choudhury. 2012. Herpetofauna of Katerniaghat Wildlife Sanctuary, Uttar Pradesh, India. Journal of Threatened Taxa 4: 2553–2568. started calling after 1830 h. Amplecting pairs constructed Davis, R.A. and R.H.L. Disney. 2003. Natural history and description of Aphiura breviceps Schmitz, a scuttle fly (Diptera: Phoridae) whose larvae prey on foam nests at the bases of cattails or under grass near tempo- the eggs of frogs (Anura: Myobatrachidae) in Western Australia. Austral rary puddles, probably to minimize the risk of desiccation if Entomology 42: 18–21. exposed to direct sunlight. Deuti, K., B.H.C.K. Murthy, and P.G.S. Sethy. 2018. A new distribution record of Polypedates taeniatus (Amphibia: Anura: Rhacophoridae) with notes on its On 20 August 2018, we found some cream-colored lar- breeding call and post-embryonic developmental stages. Records of Zoological vae in a fresh foam nest that had been constructed during the Survey of India 118: 298–306. previous night. Those larvae, 4.6–10.0 mm (mean = 6.2 ± 2.6 Filadelfo, T., B.Q. Carvalho-Zimbres, P.D. Dantas, C.A. Mello-Patiu, and R. Albuquerque-Brandão. 2013. Egg clutches and predation of Phyllomedusa mm, n = 4) in length, had consumed the entire egg mass. We azurea (Anura, Hylidae) nests in a temporary pond in central Brazil. identified the predatory larvae (Fig. 2) as flesh flies (Diptera: Herpetology Notes 6: 485–488. Sarcophagidae) using keys in Gómez-Hoyos et al. (2012), Gómez-Hoyos, D.A., T. Suárez-Joaqui, and O.H. Marín-Gómez. 2012. Flesh fly myiasis (Diptera: Sarcophagidae) in Pristimantis thectopternus (Anura: Szpila et al. (2015), and da Silva et al. (2019). Sarcophagid Strabomantidae) from Colombia. Herpetology Notes 5: 27–29. larvae can be differentiated from the larvae of flies in other Karraker, N.E. 2013. Shading mediates the interaction between an amphibian and dipteran families by the position of the posterior spiracles a predatory fly. Herpetologica 69: 257–264. Kusano, T., A. Sakai, and S. Hatanaka. 2005. Natural egg mortality and clutch size in a concave spiracular field (da Silva et al. 2019). We were of the Japanese treefrog, Rhacophorus arboreus (Amphibia: Rhacophoridae). unable to identify these larvae to a lower taxonomic level as Current Herpetology 24: 79–84. differentiation is possible only with adults (Mello-Patiu and Lin, S., C. Kuo, and K. Lue. 2000. Oviposition behavior and host selection of the frogfly,
Recommended publications
  • Impacts of the Toba Eruption and Montane Forest Expansion on Diversification in Sumatran
    bioRxiv preprint doi: https://doi.org/10.1101/843664; this version posted March 18, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. 1 Original Article Impacts of the Toba eruption and montane forest expansion on diversification in Sumatran parachuting frogs (Rhacophorus) Running head: Demography of Toba eruption Kyle A. O’Connell*1,2,3,4, Jamie R. Oaks5, Amir Hamidy6, Kyle J. Shaney7, Nia Kurniawan8, Eric N. Smith3, Matthew K. Fujita3 1Global Genome Initiative, National Museum of Natural History, Smithsonian Institute, Washington, DC, 20560, USA. 2Division of Amphibians and Reptiles, Department of Vertebrate Zoology, National Museum of Natural History, Smithsonian Institute, Washington, DC, 20560, USA. 3Department of Biology and Amphibian and Reptile Diversity Research Center, The University of Texas at Arlington, Arlington, Texas 76019, USA 4Department of Biological Sciences, The George Washington University, Washington, DC, 20052 5Department of Biological Sciences and Museum of Natural History, Auburn University, Auburn, Alabama 36849 6Zoology Division, Museum Zoologicum Bogoriense, Research Center for Biology, Indonesian Institute of Sciences. Gd. Widyasatwaloka Jl. Raya Jakarta Bogor km 46 Cibinong, Bogor, West Java, Indonesia. 7Institute of Ecology, National Autonomous University of Mexico, Mexico City, Mexico. bioRxiv preprint doi: https://doi.org/10.1101/843664; this version posted March 18, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity.
    [Show full text]
  • Diet Composition and Overlap in a Montane Frog Community in Vietnam
    Herpetological Conservation and Biology 13(1):205–215. Submitted: 5 November 2017; Accepted: 19 March 2018; Published 30 April 2018. DIET COMPOSITION AND OVERLAP IN A MONTANE FROG COMMUNITY IN VIETNAM DUONG THI THUY LE1,4, JODI J. L. ROWLEY2,3, DAO THI ANH TRAN1, THINH NGOC VO1, AND HUY DUC HOANG1 1Faculty of Biology and Biotechnology, University of Science, Vietnam National University-HCMC, 227 Nguyen Van Cu Street, District 5, Ho Chi Minh City, Vietnam 2Australian Museum Research Institute, Australian Museum,1 William Street, Sydney, New South Wales 2010, Australia 3Centre for Ecosystem Science, School of Biological, Earth and Environmental Sciences, University of New South Wales, Sydney, New South Wales 2052, Australia 4Corresponding author, e-mail: [email protected] Abstract.—Southeast Asia is home to a highly diverse and endemic amphibian fauna under great threat. A significant obstacle to amphibian conservation prioritization in the region is a lack of basic biological information, including the diets of amphibians. We used stomach flushing to obtain data on diet composition, feeding strategies, dietary niche breadth, and overlap of nine species from a montane forest in Langbian Plateau, southern Vietnam: Feihyla palpebralis (Vietnamese Bubble-nest Frog), Hylarana montivaga (Langbian Plateau Frog), Indosylvirana milleti (Dalat Frog), Kurixalus baliogaster (Belly-spotted Frog), Leptobrachium pullum (Vietnam Spadefoot Toad), Limnonectes poilani (Poilane’s Frog), Megophrys major (Anderson’s Spadefoot Toad), Polypedates cf. leucomystax (Common Tree Frog), and Raorchestes gryllus (Langbian bubble-nest Frog). To assess food selectivity of these species, we sampled available prey in their environment. We classified prey items into 31 taxonomic groups. Blattodea was the dominant prey taxon for K.
    [Show full text]
  • (Rhacophoridae, Pseudophilautus) in Sri Lanka
    Molecular Phylogenetics and Evolution 132 (2019) 14–24 Contents lists available at ScienceDirect Molecular Phylogenetics and Evolution journal homepage: www.elsevier.com/locate/ympev Diversification of shrub frogs (Rhacophoridae, Pseudophilautus) in Sri Lanka T – Timing and geographic context ⁎ Madhava Meegaskumburaa,b,1, , Gayani Senevirathnec,1, Kelum Manamendra-Arachchid, ⁎ Rohan Pethiyagodae, James Hankenf, Christopher J. Schneiderg, a College of Forestry, Guangxi Key Lab for Forest Ecology and Conservation, Guangxi University, Nanning 530004, PR China b Department of Molecular Biology & Biotechnology, Faculty of Science, University of Peradeniya, Peradeniya, Sri Lanka c Department of Organismal Biology & Anatomy, University of Chicago, Chicago, IL, USA d Postgraduate Institute of Archaeology, Colombo 07, Sri Lanka e Ichthyology Section, Australian Museum, Sydney, NSW 2010, Australia f Museum of Comparative Zoology, Harvard University, Cambridge, MA 02138, USA g Department of Biology, Boston University, Boston, MA 02215, USA ARTICLE INFO ABSTRACT Keywords: Pseudophilautus comprises an endemic diversification predominantly associated with the wet tropical regions ofSri Ancestral-area reconstruction Lanka that provides an opportunity to examine the effects of geography and historical climate change on diversi- Biogeography fication. Using a time-calibrated multi-gene phylogeny, we analyze the tempo of diversification in thecontextof Ecological opportunity past climate and geography to identify historical drivers of current patterns of diversity and distribution. Molecular Diversification dating suggests that the diversification was seeded by migration across a land-bridge connection from India duringa Molecular dating period of climatic cooling and drying, the Oi-1 glacial maximum around the Eocene-Oligocene boundary. Lineage- Speciation through-time plots suggest a gradual and constant rate of diversification, beginning in the Oligocene and extending through the late Miocene and early Pliocene with a slight burst in the Pleistocene.
    [Show full text]
  • Anura, Rhacophoridae)
    Zoologica Scripta Patterns of reproductive-mode evolution in Old World tree frogs (Anura, Rhacophoridae) MADHAVA MEEGASKUMBURA,GAYANI SENEVIRATHNE,S.D.BIJU,SONALI GARG,SUYAMA MEEGASKUMBURA,ROHAN PETHIYAGODA,JAMES HANKEN &CHRISTOPHER J. SCHNEIDER Submitted: 3 December 2014 Meegaskumbura, M., Senevirathne, G., Biju, S. D., Garg, S., Meegaskumbura, S., Pethiya- Accepted: 7 May 2015 goda, R., Hanken, J., Schneider, C. J. (2015). Patterns of reproductive-mode evolution in doi:10.1111/zsc.12121 Old World tree frogs (Anura, Rhacophoridae). —Zoologica Scripta, 00, 000–000. The Old World tree frogs (Anura: Rhacophoridae), with 387 species, display a remarkable diversity of reproductive modes – aquatic breeding, terrestrial gel nesting, terrestrial foam nesting and terrestrial direct development. The evolution of these modes has until now remained poorly studied in the context of recent phylogenies for the clade. Here, we use newly obtained DNA sequences from three nuclear and two mitochondrial gene fragments, together with previously published sequence data, to generate a well-resolved phylogeny from which we determine major patterns of reproductive-mode evolution. We show that basal rhacophorids have fully aquatic eggs and larvae. Bayesian ancestral-state reconstruc- tions suggest that terrestrial gel-encapsulated eggs, with early stages of larval development completed within the egg outside of water, are an intermediate stage in the evolution of ter- restrial direct development and foam nesting. The ancestral forms of almost all currently recognized genera (except the fully aquatic basal forms) have a high likelihood of being ter- restrial gel nesters. Direct development and foam nesting each appear to have evolved at least twice within Rhacophoridae, suggesting that reproductive modes are labile and may arise multiple times independently.
    [Show full text]
  • Predation of Feihyla Hansenae (Hansen's Bush Frog) Eggs by A
    NATURAL HISTORY NOTE The Herpetological Bulletin 139, 2017: 36-37 Predation of Feihyla hansenae (Hansen’s bush frog) eggs by a nursery web spider SINLAN POO1,2*, FRANCESCA T. ERICKSON3, SARA A. MASON4 & BRADLEY D. NISSEN5 1Memphis Zoo, 2000 Prentiss Place, Memphis, Tennessee 38112, USA 2Sakaerat Environmental Research Station, Wang Nam Khieo, Nakhon Ratchasima 30370, Thailand. 3U.S. Geological Survey Brown Treesnake Project, P.O. Box 8255 MOU-3, Dededo, 96912 Guam. 4Nicholas Institute for Environmental Policy Solutions, Duke University, Durham, North Carolina 27710, USA. 5Watershed Protection Department, City of Austin, 505 Barton Springs Road, Austin, Texas 78704, USA. *Corresponding author Email: [email protected] eihyla hansenae (Cochran, 1927) is an arboreal- breeding frog distributed in Thailand, Cambodia, and FMyanmar (Taylor, 1962; Aowphol et al., 2013). Eggs are laid in a gelatinous hemispherical clutch overhanging ponds and are cared for by female frogs until they hatch (Average egg stage = 5 days). Maternal care, viz. suppling water (Poo & Bickford, 2013) and deterring invertebrate predators (Poo et al., 2016a), is essential to the development and survival of eggs. The primary source of egg mortality is predation (Poo & Bickford, 2013). Known egg predators include ants, katydids, and snakes (Poo & Bickford, 2013; Poo et al., 2016b). In cases of partial clutch predation, threats from egg predators can lead to premature hatching in F. hansenae (Poo & Bickford, 2014), which can negatively affect the fitness and survival of hatchlings in subsequent Figure 1. Predation of F. hansenae egg clutch by N. cf. life stages (Gomez-Mestre & Warkentin, 2007). albocinctus. Here, we report the first observation of F.
    [Show full text]
  • Distribution of Anuran Species in Loboc Watershed of Bohol Island, Philippines
    Vol. 3 January 2012Asian Journal of Biodiversity Asian Journal of Biodiversity CHED Accredited Research Journal, Category A Art. #86, pp.126-141 Print ISSN 2094-1519 • Electronic ISSN 2244-0461 doi: http://dx.doi.org/10.7828/ajob.v3i1.86 Distribution of Anuran Species in Loboc Watershed of Bohol Island, Philippines REIZL P. JOSE [email protected] Bohol Island State University, Bilar Campus, Bohol, Philippines +63 928-3285009 Date Submitted: Jan. 8, 2011 Final Revision Accepted: March 14, 2011 Abstract - The Philippines is rich in biodiversity and Bohol Island is among the many places in the country requiring attention for conservation efforts. For this reason, a survey o f anurans was conducted in Loboc Watershed, the forest reserve in the island. Different sampling techniques were used. Three transect lines was established and were positioned perpendicular to water bodies parallel to the existing trails. A 10x10 meter quadrat size was established along each transect line. A visual encounter technique was used along each established quadrat and identification was done using a field guide. Fifteen species of anurans were recorded. One species belongs to families Bufonidae (Bufo marinus) and Megophryidae (Megophryis stejnegeri); two to family Microhylidae (Kalophrynus pleurostigma and Kaluola picta); six family Ranidae (Fejervarya cancrivora, Limnonectes leytensis, Limnonectes magnus, Platymantis guentheri, Playmantis corrugatus, and Rana grandocula) and five Rhacophoridae (Nyctixalus spinosus, Polypedates leucomystax leucomystax, Polypedates leucomystax quadrilineatus, Rhacophorus appendiculatus and Rhacoporus pardalis). The disturbed nature of the area still recorded endemic and threatened species. This suggests that forests and critical habitats in the area need to be protected and conserved. 126 Distribution of Anuran Species in Loboc Watershed..
    [Show full text]
  • Vertical and Horizontal Trophic Networks in the Aroid-Infesting Insect Community of Los Tuxtlas Biosphere Reserve, Mexico
    insects Article Vertical and Horizontal Trophic Networks in the Aroid-Infesting Insect Community of Los Tuxtlas Biosphere Reserve, Mexico Guadalupe Amancio 1 , Armando Aguirre-Jaimes 1, Vicente Hernández-Ortiz 1,* , Roger Guevara 2 and Mauricio Quesada 3,4 1 Red de Interacciones Multitróficas, Instituto de Ecología A.C., Xalapa, Veracruz 91073, Mexico 2 Red de Biologia Evolutiva, Instituto de Ecología A.C., Xalapa, Veracruz 91073, Mexico 3 Laboratorio Nacional de Análisis y Síntesis Ecológica, Escuela Nacional de Estudios Superiores Unidad Morelia, Universidad Nacional Autónoma de México, Morelia 58190 Michoacán, Mexico 4 Instituto de Investigaciones en Ecosistemas y Sustentabilidad, Universidad Nacional Autónoma de México, Morelia 58190 Michoacán, Mexico * Correspondence: [email protected] Received: 20 June 2019; Accepted: 9 August 2019; Published: 15 August 2019 Abstract: Insect-aroid interaction studies have focused largely on pollination systems; however, few report trophic interactions with other herbivores. This study features the endophagous insect community in reproductive aroid structures of a tropical rainforest of Mexico, and the shifting that occurs along an altitudinal gradient and among different hosts. In three sites of the Los Tuxtlas Biosphere Reserve in Mexico, we surveyed eight aroid species over a yearly cycle. The insects found were reared in the laboratory, quantified and identified. Data were analyzed through species interaction networks. We recorded 34 endophagous species from 21 families belonging to four insect orders. The community was highly specialized at both network and species levels. Along the altitudinal gradient, there was a reduction in richness and a high turnover of species, while the assemblage among hosts was also highly specific, with different dominant species.
    [Show full text]
  • Amphibian Community Structure Along Elevation Gradients in Eastern Nepal Himalaya Janak R
    Khatiwada et al. BMC Ecol (2019) 19:19 https://doi.org/10.1186/s12898-019-0234-z BMC Ecology RESEARCH ARTICLE Open Access Amphibian community structure along elevation gradients in eastern Nepal Himalaya Janak R. Khatiwada1,2, Tian Zhao1* , Youhua Chen1, Bin Wang1, Feng Xie1, David C. Cannatella3 and Jianping Jiang1 Abstract Background: Species richness and composition pattern of amphibians along elevation gradients in eastern Nepal Himalaya are rarely investigated. This is a frst ever study in the Himalayan elevation gradient, the world’s highest mountain range and are highly sensitive to the efects of recent global changes. The aim of the present study was to assess amphibian community structure along elevation gradients and identify the potential drivers that regulate community structures. Amphibian assemblages were sampled within 3 months in both 2014 and 2015 (from May to July) using nocturnal time constrained and acoustic aids visual encounter surveys. In total, 79 transects between 78 and 4200 m asl were sampled within 2 years feld work. A combination of polynomial regression, generalized linear models, hierarchical partitioning and canonical correspondence analysis were used to determine the efects of eleva- tion and environmental variables on species richness, abundance, and composition of amphibian communities. Results: Species richness and abundance declined linearly with increasing elevation, which did not support the Mid- Domain Model. Among all the environmental variables, elevation, surface area and humidity were the best predictors of species richness, abundance and composition of amphibians. The majority of amphibian species had narrow eleva- tion ranges. There was no signifcant correlation between species range size and elevation gradients.
    [Show full text]
  • AMPHIBIANS and REPTILES of Morningside, Sri Lanka
    AMPHIBIANS and REPTILES of Morningside, Sri Lanka 1 Peter Janzen Justus-von-Liebig-Schule, Duisburg, Germany Photos: Peter Janzen © Peter Janzen [[email protected]] Male (M), Female (F), Juvenile (Juv.), Endemic (E) and Poisonous (P). [fieldguides.fieldmuseum.org] [1061] version 1 3/2019 1 Adenomus kelaartii (E) 2 Duttaphrynus melanostictus 3 Euphlyctis cyanophlyctis 4 Euphlyctis cyanophlyctis BUFONIDAE BUFONIDAE DICROGLOSSIDAE DICROGLOSSIDAE 5 Fejervarya kirtisinghei (E) 6 Fejervarya kirtisinghei (E) 7 Fejervarya kirtisinghei (E) 8 Microhyla karunaratnei (E) DICROGLOSSIDAE DICROGLOSSIDAE DICROGLOSSIDAE MICROHYLIDAE 9 Microhyla karunaratnei (E) 10 Microhyla karunaratnei (E) 11 Uperodon obscurus (E) 12 Uperodon obscurus (E) MICROHYLIDAE MICROHYLIDAE MICROHYLIDAE MICROHYLIDAE 13 Uperodon obscurus (E) 14 Uperodon obscurus (E) 15 Lankanectes corrugatus (E) 16 Indosylvirana temporalis MICROHYLIDAE MICROHYLIDAE NYCTIBATRACHIDAE RANIDAE 17 Indosylvirana temporalis 18 Indosylvirana temporalis 19 Indosylvirana temporalis 20 Indosylvirana temporalis RANIDAE RANIDAE RANIDAE RANIDAE AMPHIBIANS and REPTILES of Morningside, Sri Lanka 2 Peter Janzen Justus-von-Liebig-Schule, Duisburg, Germany Photos: Peter Janzen © Peter Janzen [[email protected]] Male (M), Female (F), Juvenile (Juv.), Endemic (E) and Poisonous (P). [fieldguides.fieldmuseum.org] [1061] version 1 3/2019 21 Indosylvirana temporalis 22 Indosylvirana temporalis 23 Polypedates cruciger (E) 24 Polypedates cruciger (E) RANIDAE RANIDAE RHACOPHORIDAE RHACOPHORIDAE 25 Polypedates cruciger (E) 26 Polypedates
    [Show full text]
  • Diptera: Drosophilidae)
    Zootaxa 1069: 1–32 (2005) ISSN 1175-5326 (print edition) www.mapress.com/zootaxa/ ZOOTAXA 1069 Copyright © 2005 Magnolia Press ISSN 1175-5334 (online edition) Molecular systematics and geographical distribution of the Drosophila longicornis species complex (Diptera: Drosophilidae) DEODORO C. S. G. OLIVEIRA1, 2, PATRICK M. O’GRADY1, 3, WILLIAM J. ETGES4, WILLIAM B. HEED5 & ROB DeSALLE1 1Division of Invertebrate Zoology, American Museum of Natural History, New York, NY, USA; email: [email protected] 2Department of Biology, University of Rochester, Rochester, NY, USA; email: [email protected] 3Department of Biology, University of Vermont, VT, USA; email: [email protected] 4Department of Biological Sciences, University of Arkansas, Fayetteville, AR, USA; email: [email protected] 5Department of Ecology and Evolutionary Biology, The University of Arizona, Tucson, AZ, USA; email: [email protected] Abstract Here we examine the phylogenetic relationships of eleven species previously hypothesized to be members of the Drosophila longicornis complex (repleta group, mulleri subgroup) using combined analyses of four mitochondrial genes. This complex, as currently redefined, is composed of the longicornis cluster (D. longicornis, D. pachuca, D. propachuca, and D. mainlandi), the ritae cluster (D. desertorum, D. mathisi, and D. ritae), and several miscellaneous species (D. hamatofila, D. hexastigma, D. spenceri, and an undescribed species “from Sonora”). A maximum likelihood inference also includes the huckinsi cluster (D. huckinsi and D. huichole) as the most distant members in the longicornis complex, a condition not recovered using maximum parsimony. We were unable to diagnose species in the triad of sibling species D. longicornis, D. pachuca, and D. propachuca using rapidly evolving mitochondrial DNA data, and we discuss possible species concept conflict for this triad.
    [Show full text]
  • Refuse Containers As a Source of Flies in Honolulu and Nearby Communities
    Vol. XVII, No. 3, August, 1961 477 Refuse Containers as a Source of Flies in Honolulu and Nearby Communities Donald P. Wilton DIVISION OF SANITATION HAWAII STATE DEPARTMENT OF HEALTH HONOLULU, HAWAII {Submitted for publication December, I960) The garbage can has long been recognized as an important site of domestic fly production. Quarterman et al. (1949) found garbage cans second only to the city dump as a source of flies in Savannah, Georgia. They reported fly breeding in or under 60 per cent of the containers examined. Fifty per cent of the infested media detected by Schoof et al. (1954) in fly breeding surveys conducted in Charleston, West Virginia were garbage. A similar situation was found by Siverly and Schoof (1955) in Phoenix, Arizona. Kilpatrick and Bogue (1956) demonstrated fly emergence from ground surfaces under and near garbage cans at Mission and Pharr, Texas. As an illustration of the significance of garbage as a breeding medium for domestic flies, it was stated by Siverly and Schoof (1955) that as many as 70,000 flies have been produced by one cubic foot of this material. Campbell and Black (i960) reporting on an investigation of prepupal migration of fly larvae from refuse containers in Concord, California recommended twice-a- week refuse collection during hot weather. They suggested that this would remove refuse before any significant migration (and hence, any significant fly production) could occur. Often, however, routine refuse collection fails to remove all the material in the can. As pointed out by Quarterman et al. (1949), a sludge-like deposit which is not dislodged when the container is upended frequently builds up in the bottoms of neglected cans.
    [Show full text]
  • Trapping Drosophila Repleta (Diptera: Drosophilidae) Using Color and Volatiles B
    Trapping Drosophila repleta (Diptera: Drosophilidae) using color and volatiles B. A. Hottel1,*, J. L. Spencer1 and S. T. Ratcliffe3 Abstract Color and volatile stimulus preferences of Drosophila repleta (Patterson) Diptera: Drosophilidae), a nuisance pest of swine and poultry facilities, were tested using sticky card and bottle traps. Attractions to red, yellow, blue, orange, green, purple, black, grey and a white-on-black contrast treatment were tested in the laboratory. Drosophila repleta preferred red over yellow and white but not over blue. Other than showing preferences over the white con- trol, D. repleta was not observed to have preferences between other colors and shade combinations. Pinot Noir red wine, apple cider vinegar, and wet swine feed were used in volatile preference field trials. Red wine was more attractiveD. to repleta than the other volatiles tested, but there were no dif- ferences in response to combinations of a red wine volatile lure and various colors. Odor was found to play the primary role in attracting D. repleta. Key Words: Drosophila repleta; color preference; volatile preference; trapping Resumen Se evaluaron las preferencias de estímulo de volátiles y color de Drosophila repleta (Patterson) (Diptera: Drosophilidae), una plaga molesta en las instalaciones porcinas y avícolas, utilzando trampas de tarjetas pegajosas y de botella. Su atracción a los tratamientos de color rojo, amarillo, azul, anaranjado, verde, morado, negro, gris y un contraste de blanco sobre negro fue probado en el laboratorio. Drosophila repleta preferio el rojo mas que el amarillo y el blanco, pero no sobre el azul. Aparte de mostrar una preferencia por el control de color blanco, no se observó que D.
    [Show full text]