The 1999 List of Threatened Fauna and Flora of Sri Lanka
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Gliding Dragons and Flying Squirrels: Diversifying Versus Stabilizing Selection on Morphology Following the Evolution of an Innovation
vol. 195, no. 2 the american naturalist february 2020 E-Article Gliding Dragons and Flying Squirrels: Diversifying versus Stabilizing Selection on Morphology following the Evolution of an Innovation Terry J. Ord,1,* Joan Garcia-Porta,1,† Marina Querejeta,2,‡ and David C. Collar3 1. Evolution and Ecology Research Centre and the School of Biological, Earth and Environmental Sciences, University of New South Wales, Kensington, New South Wales 2052, Australia; 2. Institute of Evolutionary Biology (CSIC–Universitat Pompeu Fabra), Passeig Marítim de la Barceloneta, 37–49, Barcelona 08003, Spain; 3. Department of Organismal and Environmental Biology, Christopher Newport University, Newport News, Virginia 23606 Submitted August 1, 2018; Accepted July 16, 2019; Electronically published December 17, 2019 Online enhancements: supplemental material. Dryad data: https://doi.org/10.5061/dryad.t7g227h. fi abstract: Evolutionary innovations and ecological competition are eral de nitions of what represents an innovation have been factors often cited as drivers of adaptive diversification. Yet many offered (reviewed by Rabosky 2017), this classical descrip- innovations result in stabilizing rather than diversifying selection on tion arguably remains the most useful (Galis 2001; Stroud morphology, and morphological disparity among coexisting species and Losos 2016; Rabosky 2017). Hypothesized innovations can reflect competitive exclusion (species sorting) rather than sympat- have drawn considerable attention among ecologists and ric adaptive divergence (character displacement). We studied the in- evolutionary biologists because they can expand the range novation of gliding in dragons (Agamidae) and squirrels (Sciuridae) of ecological niches occupied within communities. In do- and its effect on subsequent body size diversification. We found that gliding either had no impact (squirrels) or resulted in strong stabilizing ing so, innovations are thought to be important engines of selection on body size (dragons). -
A Compilation and Analysis of Food Plants Utilization of Sri Lankan Butterfly Larvae (Papilionoidea)
MAJOR ARTICLE TAPROBANICA, ISSN 1800–427X. August, 2014. Vol. 06, No. 02: pp. 110–131, pls. 12, 13. © Research Center for Climate Change, University of Indonesia, Depok, Indonesia & Taprobanica Private Limited, Homagama, Sri Lanka http://www.sljol.info/index.php/tapro A COMPILATION AND ANALYSIS OF FOOD PLANTS UTILIZATION OF SRI LANKAN BUTTERFLY LARVAE (PAPILIONOIDEA) Section Editors: Jeffrey Miller & James L. Reveal Submitted: 08 Dec. 2013, Accepted: 15 Mar. 2014 H. D. Jayasinghe1,2, S. S. Rajapaksha1, C. de Alwis1 1Butterfly Conservation Society of Sri Lanka, 762/A, Yatihena, Malwana, Sri Lanka 2 E-mail: [email protected] Abstract Larval food plants (LFPs) of Sri Lankan butterflies are poorly documented in the historical literature and there is a great need to identify LFPs in conservation perspectives. Therefore, the current study was designed and carried out during the past decade. A list of LFPs for 207 butterfly species (Super family Papilionoidea) of Sri Lanka is presented based on local studies and includes 785 plant-butterfly combinations and 480 plant species. Many of these combinations are reported for the first time in Sri Lanka. The impact of introducing new plants on the dynamics of abundance and distribution of butterflies, the possibility of butterflies being pests on crops, and observations of LFPs of rare butterfly species, are discussed. This information is crucial for the conservation management of the butterfly fauna in Sri Lanka. Key words: conservation, crops, larval food plants (LFPs), pests, plant-butterfly combination. Introduction Butterflies go through complete metamorphosis 1949). As all herbivorous insects show some and have two stages of food consumtion. -
Frontiers in Zoology Biomed Central
Frontiers in Zoology BioMed Central Research Open Access Does the DNA barcoding gap exist? – a case study in blue butterflies (Lepidoptera: Lycaenidae) Martin Wiemers* and Konrad Fiedler Address: Department of Population Ecology, Faculty of Life Sciences, University of Vienna, Althanstrasse 14, 1090 Vienna, Austria Email: Martin Wiemers* - [email protected]; Konrad Fiedler - [email protected] * Corresponding author Published: 7 March 2007 Received: 1 December 2006 Accepted: 7 March 2007 Frontiers in Zoology 2007, 4:8 doi:10.1186/1742-9994-4-8 This article is available from: http://www.frontiersinzoology.com/content/4/1/8 © 2007 Wiemers and Fiedler; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Abstract Background: DNA barcoding, i.e. the use of a 648 bp section of the mitochondrial gene cytochrome c oxidase I, has recently been promoted as useful for the rapid identification and discovery of species. Its success is dependent either on the strength of the claim that interspecific variation exceeds intraspecific variation by one order of magnitude, thus establishing a "barcoding gap", or on the reciprocal monophyly of species. Results: We present an analysis of intra- and interspecific variation in the butterfly family Lycaenidae which includes a well-sampled clade (genus Agrodiaetus) with a peculiar characteristic: most of its members are karyologically differentiated from each other which facilitates the recognition of species as reproductively isolated units even in allopatric populations. -
Zoologische Mededelingen Uitgegeven Door Het
ZOOLOGISCHE MEDEDELINGEN UITGEGEVEN DOOR HET RIJKSMUSEUM VAN NATUURLIJKE HISTORIE TE LEIDEN (MINISTERIE VAN CULTUUR, RECREATIE EN MAATSCHAPPELIJK WERK) Deel 56 no. 10 7 mei 1982 NOMENCLATURAL PROBLEMS RELATING TO ATRACTUS TRILINEATUS WAGLER, 1828 by M. S. HOOGMOED Rijksmuseum van Natuurlijke Historie, Leiden, The Netherlands INTRODUCTION The Rijksmuseum van Natuurlijke Historie material of Brachyorrhos albus (L., 1758), which had been on loan to Dr. S. B. McDowell, New York, was returned to us with the remark that reg.no. RMNH 48 from Java certainly did not belong to that species. Dr. McDowell suggested it might be an Atractus, and following his suggestion I examined this specimen. It soon became evident that Dr. McDowell had been right and that the specimen did belong to Atractus trilineatus Wagler, a species only known from Trinidad, eastern Venezuela and western Guyana (Hoogmoed, 1979: 275). HISTORY The specimen concerned (RMNH 48) belongs to the oldest part of the collec- tion of the RMNH. It turned out to have been investigated by many ancient authors and it was discovered that it is a type specimen of several nominal species. Before trying to reconstruct the history of this specimen it seems useful to give a short description. It is a female with a total length of 205 mm, the snout-vent length is 194 mm, the tail length 11 mm. Ventrals 142, anal undivid- ed, 11 subcaudals in two rows. Upper labials eight, of which the fourth and the fifth touch the eye, two postoculars, no preocular, temporals 1 + 2, lower labials eight, of which four are in contact with the chinshields. -
The Superfamily Calopterygoidea in South China: Taxonomy and Distribution. Progress Report for 2009 Surveys Zhang Haomiao* *PH D
International Dragonfly Fund - Report 26 (2010): 1-36 1 The Superfamily Calopterygoidea in South China: taxonomy and distribution. Progress Report for 2009 surveys Zhang Haomiao* *PH D student at the Department of Entomology, College of Natural Resources and Environment, South China Agricultural University, Guangzhou 510642, China. Email: [email protected] Introduction Three families in the superfamily Calopterygoidea occur in China, viz. the Calo- pterygidae, Chlorocyphidae and Euphaeidae. They include numerous species that are distributed widely across South China, mainly in streams and upland running waters at moderate altitudes. To date, our knowledge of Chinese spe- cies has remained inadequate: the taxonomy of some genera is unresolved and no attempt has been made to map the distribution of the various species and genera. This project is therefore aimed at providing taxonomic (including on larval morphology), biological, and distributional information on the super- family in South China. In 2009, two series of surveys were conducted to Southwest China-Guizhou and Yunnan Provinces. The two provinces are characterized by karst limestone arranged in steep hills and intermontane basins. The climate is warm and the weather is frequently cloudy and rainy all year. This area is usually regarded as one of biodiversity “hotspot” in China (Xu & Wilkes, 2004). Many interesting species are recorded, the checklist and photos of these sur- veys are reported here. And the progress of the research on the superfamily Calopterygoidea is appended. Methods Odonata were recorded by the specimens collected and identified from pho- tographs. The working team includes only four people, the surveys to South- west China were completed by the author and the photographer, Mr. -
Ecology and Demography of the Critically Endangered Kandian Torrent Toad Adenomus Kandianus: a Long-Lost Endemic Species of Sri Lanka
Ecology and demography of the Critically Endangered Kandian torrent toad Adenomus kandianus: a long-lost endemic species of Sri Lanka S URANJAN K ARUNARATHNA,SUJAN H ENKANATHTHEGEDARA,DINESH G ABADAGE M ADHAVA B OTEJUE,MAJINTHA M ADAWALA and T HILINA D. SURASINGHE Abstract The tropical island nation of Sri Lanka is a bio- Keywords Adenomus kandianus, Amphibia, Bufonidae, diversity hotspot with a high diversity and endemism of am- conservation, Critically Endangered, montane streams, phibians. The endemic, stream-dwelling Kandian torrent Sri Lanka, tropical rainforests toad Adenomus kandianus is Critically Endangered and was considered to be extinct until its rediscovery in . The species is now known from two localities in tropical Introduction montane forests. We conducted a -year study using tran- sect surveys and opportunistic excursions to assess habitat he South Asian tropical island of Sri Lanka is rich in associations, demographics and abundance of A. kandianus Tamphibian diversity (Meegaskumbura et al., ). in and around Pidurutalagala Conservation Forest. We re- Of the country’s described amphibian species corded a mean of . post-metamorphs per year, with a (c. %) are endemic and . % are restricted to rainforests density of , individual per m , with occurrence within (Surasinghe, ; Wickramasinghe et al., ). Sri Lanka’s a narrow extent (c. km ) of the stream channel. amphibians are threatened by deforestation, environmental Behaviour and microhabitat selection varied depending on pollution and road traffic (Pethiyagoda et al., ; sex and stage of maturity. The species preferred moderately Karunarathna et al., ). These anthropogenic stressors have sized montane streams with rocky substrates and woody contributed to the extinction of amphibian species, and de- debris, colder temperatures, and closed-canopy, intact ri- clining populations of nearly half of the extant species (MOE, parian forests. -
A Manual for Commercial Production of the Tiger Barb, ~C~T Etnlnmmi
saeAU-8-97-002 C3 A Manual for Commercial Production of the Tiger Barb, ~c~t etnlnmmI. A T p y P i d T k Sp By: Clyde S. Tamaru, Ph.D. Brian Cole, M.S. Richard Bailey, B.A. Christopher Brown, Ph.o. Center for Tropical and Subtropical Aquaculture Publication Number 129 Commercial Production of Tiger 8arbs ACKNOWLEDGEMENTS This manual is a combined effort of three institutions, United States Department of Agriculture Center for Tropical and Subtropical Aquaculture CTSA!, and University of Hawaii Sea Grant Extension Service SGES! and Aquaculture Development Program ADP!, Department of Land and Natural Resources, State of Hawaii. Financial support for this project was provided by the Center for Tropical and Subtropical Aquaculture through grants from the US Department of Agriculture USDA grant numbers 93-38500-8583 and 94-38500-0065!. Production of the manual is also funded in part by a grant from the National Oceanic and Atmospheric Administration, project kA/AS-1 which is sponsored by the University of Hawaii Sea Grant College Program, School of Ocean Earth Science and Technology SOEST!, under institutional Grant No. NA36RG0507 from NOAA Office of Sea Grant, Department of Commerce, UNIHI-SEAGRANT-TR-96-01. Support for the production of the manual was also provided by the Aquaculture Development Program, Department of Land and Natural Resources, State of Hawaii, as part of their Aquaculture Extension Project with University of Hawaii Sea Grant Extension, Service Contract Nos. 9325 and 9638. The views expressed herein are those of the authors and do not necessarily reflect the views of USDA or any of its sub-agencies. -
Are Represented by 47 Spp. India’S Independence,Pp
Odonatological Abstracts 1997 mation Lanthus and abundance on sp. Cordulegastersp. and biomass is included. (14416) ALFRED, J.R.B. & A. KUMAR, 1997. Fauna 1998 ofDelhi: faunal analysis (basedon available data). Slate Fauna Ser. zool. Surv. India 6: 891-903. — (Second Author: Northern Regional Stn, Zool. Surv. India, (14420) ALFRED, A.K. DAS & A.K. Dehra Dun-248195,India). SANYAL, [Eds], 1998. [Faunal diversity in India:] Odonata. In\ J.R.B. Alfred Faunal A tabelar review of animal spp. recorded from Delhi, et al., [Eds], diversity fam. The odon. in India: commemorative volume in the 50th India;no species lists, numbers per only. a year of 172-178, ENVIS Centre, are represented by 47 spp. India’s independence,pp. Zool. Surv. India, Calcutta. — (First Author: Director, (14417) KUMAR, A., 1997. Fauna of Delhi: Odonata, Zool. Surv. India, 234/4, A.J.C. Bose Rd, Calcutta- imagos. State Fauna Ser. zool. Surv. India 6: 147-159. -700020, India). in — (Northern Regional Stn, Zool. Surv. India, Dehra The earliest reference to Indian dragonflies appears Dun-248195,India). the Sangam literature, dated prior to the 8th century and known from the A revised and updatedchecklist (47 spp.) ofthe odon. AD. At present, 449 spp. sspp. are inch 4 for the first Indian 23% of which endemic. A review fauna ofDelhi, India, spp. published territory, are and is ofthe numbers of known from various time. Precise locality data, descriptive notes presented spp. for 21 remarks onbionomy are presented spp. regions, and some considerations on conservation future studies strategies and are provided. (14418) KUMAR, A., 1997. -
Summary Report of Freshwater Nonindigenous Aquatic Species in U.S
Summary Report of Freshwater Nonindigenous Aquatic Species in U.S. Fish and Wildlife Service Region 4—An Update April 2013 Prepared by: Pam L. Fuller, Amy J. Benson, and Matthew J. Cannister U.S. Geological Survey Southeast Ecological Science Center Gainesville, Florida Prepared for: U.S. Fish and Wildlife Service Southeast Region Atlanta, Georgia Cover Photos: Silver Carp, Hypophthalmichthys molitrix – Auburn University Giant Applesnail, Pomacea maculata – David Knott Straightedge Crayfish, Procambarus hayi – U.S. Forest Service i Table of Contents Table of Contents ...................................................................................................................................... ii List of Figures ............................................................................................................................................ v List of Tables ............................................................................................................................................ vi INTRODUCTION ............................................................................................................................................. 1 Overview of Region 4 Introductions Since 2000 ....................................................................................... 1 Format of Species Accounts ...................................................................................................................... 2 Explanation of Maps ................................................................................................................................ -
Marine Reptiles Arne R
Virginia Commonwealth University VCU Scholars Compass Study of Biological Complexity Publications Center for the Study of Biological Complexity 2011 Marine Reptiles Arne R. Rasmessen The Royal Danish Academy of Fine Arts John D. Murphy Field Museum of Natural History Medy Ompi Sam Ratulangi University J. Whitfield iG bbons University of Georgia Peter Uetz Virginia Commonwealth University, [email protected] Follow this and additional works at: http://scholarscompass.vcu.edu/csbc_pubs Part of the Life Sciences Commons Copyright: © 2011 Rasmussen et al. 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, provided the original author and source are credited. Downloaded from http://scholarscompass.vcu.edu/csbc_pubs/20 This Article is brought to you for free and open access by the Center for the Study of Biological Complexity at VCU Scholars Compass. It has been accepted for inclusion in Study of Biological Complexity Publications by an authorized administrator of VCU Scholars Compass. For more information, please contact [email protected]. Review Marine Reptiles Arne Redsted Rasmussen1, John C. Murphy2, Medy Ompi3, J. Whitfield Gibbons4, Peter Uetz5* 1 School of Conservation, The Royal Danish Academy of Fine Arts, Copenhagen, Denmark, 2 Division of Amphibians and Reptiles, Field Museum of Natural History, Chicago, Illinois, United States of America, 3 Marine Biology Laboratory, Faculty of Fisheries and Marine Sciences, Sam Ratulangi University, Manado, North Sulawesi, Indonesia, 4 Savannah River Ecology Lab, University of Georgia, Aiken, South Carolina, United States of America, 5 Center for the Study of Biological Complexity, Virginia Commonwealth University, Richmond, Virginia, United States of America Of the more than 12,000 species and subspecies of extant Caribbean, although some species occasionally travel as far north reptiles, about 100 have re-entered the ocean. -
Impact of Fishing with Tephrosia Candida (Fabaceae) on Diversity
Impact of fishing with Tephrosia candida (Fabaceae) on diversity and abundance of fish in the streams at the boundary of Sinharaja Man and Biosphere Forest Reserve, Sri Lanka Udaya Priyantha Kankanamge Epa & Chamari Ruvandika Waniga Chinthamanie Mohotti Department of Zoology & Environmental Management, Faculty of Science, University of Kelaniya, Kelaniya 11600, Sri Lanka; [email protected], [email protected] Received 07-V-2015. Corrected 04-III-2016. Accepted 31-III-2016. Abstract: Local communities in some Asian, African and American countries, use plant toxins in fish poisoning for fishing activities; however, the effects of this practice on the particular wild fish assemblages is unknown. This study was conducted with the aim to investigate the effects of fish poisoning using Tephrosia candida, on freshwater fish diversity and abundance in streams at the boundary of the World Natural Heritage site, Sinharaja Forest Reserve, Sri Lanka. A total of seven field trips were undertaken on a bimonthly basis, from May 2013 to June 2014. We surveyed five streams with similar environmental and climatological conditions at the boundary of Sinharaja forest. We selected three streams with active fish poisoning practices as treatments, and two streams with no fish poisoning as controls. Physico-chemical parameters and flow rate of water in selected streams were also measured at bimonthly intervals. Fish were sampled by electrofishing and nets in three randomly selected confined locations (6 x 2 m stretch) along every stream. Fish species were identified, their abundances were recorded, and Shannon-Weiner diversity index was calculated for each stream. Streams were clustered based on the Bray-Curtis similarity matrix for fish composition and abundance. -
Phylogeny and Historical Biogeography of Lauraceae
PHYLOGENY Andre'S. Chanderbali,2'3Henk van der AND HISTORICAL Werff,3 and Susanne S. Renner3 BIOGEOGRAPHY OF LAURACEAE: EVIDENCE FROM THE CHLOROPLAST AND NUCLEAR GENOMES1 ABSTRACT Phylogenetic relationships among 122 species of Lauraceae representing 44 of the 55 currentlyrecognized genera are inferredfrom sequence variation in the chloroplast and nuclear genomes. The trnL-trnF,trnT-trnL, psbA-trnH, and rpll6 regions of cpDNA, and the 5' end of 26S rDNA resolved major lineages, while the ITS/5.8S region of rDNA resolved a large terminal lade. The phylogenetic estimate is used to assess morphology-based views of relationships and, with a temporal dimension added, to reconstructthe biogeographic historyof the family.Results suggest Lauraceae radiated when trans-Tethyeanmigration was relatively easy, and basal lineages are established on either Gondwanan or Laurasian terrains by the Late Cretaceous. Most genera with Gondwanan histories place in Cryptocaryeae, but a small group of South American genera, the Chlorocardium-Mezilauruls lade, represent a separate Gondwanan lineage. Caryodaphnopsis and Neocinnamomum may be the only extant representatives of the ancient Lauraceae flora docu- mented in Mid- to Late Cretaceous Laurasian strata. Remaining genera place in a terminal Perseeae-Laureae lade that radiated in Early Eocene Laurasia. Therein, non-cupulate genera associate as the Persea group, and cupuliferous genera sort to Laureae of most classifications or Cinnamomeae sensu Kostermans. Laureae are Laurasian relicts in Asia. The Persea group