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Morphometrical Variations of Malaysian Hipposideros Species
Malaysian Journal of Mathematical Sciences 6(1): 47-57 (2012) Morphometrical Variations of Malaysian Hipposideros Species Siti Nurlydia Sazali, Charlie J. Laman and M.T. Abdullah Department of Zoology, Faculty of Resource Science and Technology, Universiti Malaysia Sarawak, 94300 Kota Samarahan, Sarawak, Malaysia E-mail: [email protected] ABSTRACT A study on the morphometrical variations among four Malaysian Hipposideros species was conducted using voucher specimens deposited in Universiti Malaysia Sarawak (UNIMAS) Zoological Museum and the Department of Widlife and National Park (DWNP) Kuala Lumpur. Twenty two individuals from four species of Hipposideros ater , H. bicolor , H. cineraceus and H. dyacorum were morphologically measured, in which a total of 27 linear parameters of body, skull and dentals of each were appropriately recorded. The statistical data were later subjected to discriminant function analysis (DFA) and canonical variate analysis (CVA) using SPSS version 15.0 and unweighted pair-group method average (UPGMA) cluster analysis using Minitab version 14.4. The highest character loadings observed in Function l, Function 2 and Function 3 were the forearm length (FA), the third digit second phalanx length (D3P2L) and the palatal length (PL) with standardised canonical discriminant function coefficient values of 21.910, 5.770 and 5.095, respectively. These three characters were identified as the best diagnostic features for discriminating these closely related species of Hipposideros . Hence, this morphometric approach could be a promising tool as an alternative to the molecular DNA analysis for identification of Chiroptera species. Keywords: Hipposideros , morphometric, discriminant function analysis cluster analysis, species identification. 1. INTRODUCTION Bats belong to the order Chiroptera and can be distinguished from all other mammals by their ability to fly, which is a result of the modification of their forelimbs into wings (Payne et al . -
Carnivores of Syria 229 Doi: 10.3897/Zookeys.31.170 RESEARCH ARTICLE Launched to Accelerate Biodiversity Research
A peer-reviewed open-access journal ZooKeys 31: 229–252 (2009) Carnivores of Syria 229 doi: 10.3897/zookeys.31.170 RESEARCH ARTICLE www.pensoftonline.net/zookeys Launched to accelerate biodiversity research Carnivores of Syria Marco Masseti Department of Evolutionistic Biology “Leo Pardi” of the University of Florence, Italy Corresponding author: Marco Masseti (marco.masseti@unifi .it) Academic editors: E. Neubert, Z. Amr | Received 14 April 2009 | Accepted 29 July 2009 | Published 28 December 2009 Citation: Masseti, M (2009) Carnivores of Syria. In: Neubert E, Amr Z, Taiti S, Gümüs B (Eds) Animal Biodiversity in the Middle East. Proceedings of the First Middle Eastern Biodiversity Congress, Aqaba, Jordan, 20–23 October 2008. ZooKeys 31: 229–252. doi: 10.3897/zookeys.31.170 Abstract Th e aim of this research is to outline the local occurrence and recent distribution of carnivores in Syria (Syrian Arab Republic) in order to off er a starting point for future studies. The species of large dimensions, such as the Asiatic lion, the Caspian tiger, the Asiatic cheetah, and the Syrian brown bear, became extinct in historical times, the last leopard being reputed to have been killed in 1963 on the Alauwit Mountains (Al Nusyriain Mountains). Th e checklist of the extant Syrian carnivores amounts to 15 species, which are essentially referable to 4 canids, 5 mustelids, 4 felids – the sand cat having been reported only recently for the fi rst time – one hyaenid, and one herpestid. Th e occurrence of the Blandford fox has yet to be con- fi rmed. Th is paper is almost entirely the result of a series of fi eld surveys carried out by the author mainly between 1989 and 1995, integrated by data from several subsequent reports and sightings by other authors. -
Legacies and Gifts
202 Oryx Oryx 100% Fund The following grants have been made from the Oryx 100% Fund: £500 to the Durham University Himalayan Expedition to complete a study of the Himalayan tahr in Langtang National Park; £500 to the University of East Anglia Nepal Expedition for surveys of the pygmy hog and hispid hare; £500 to Professor Daniel Torres-Navarro, University of Chile, for studies of the fur seal on Juan Fernandez; £300 to Katherine Homewood and Margaret Renshaw to study infant development and socialisation in the Tana mangabey, part of a con- tinuing study of this endangered monkey; £300 to Godofredo Stutzin for camera equipment and binoculars for the use of guards protecting the Chilean huemul; £250 to Dr E. O. Moll, East Illinois University, for development of a management programme for Malaysian sea and river turtles; £250 to Sompoad Srikosarmatara, Mahidol University, Bangkok, for a study of the pileated gibbon in the Khao Sqi Dao Wildlife Sanctuary; £250 to the Wildlife and Nature Protection Society of Sri Lanka to offset costs of conservation leaflets for tourists {Oryx, Dec. 1977, p.l 17); £20 to J. A. Fowler of Leicester Polytechnic for ecological studies in the maritime approaches to the Sullom Voe Oil Terminal, Shetland. Legacies and Gifts FPS is most grateful for the following gifts of £20 and over, totalling £9794, and for other smaller gifts received between October 1977 and March 1978: Legacies L. Sheriff £6300 Mrs G.H. Soward £25 Gifts Anonymous £2000 Dr A.A. Spriggs £50 Mrs V.H. Williams £25 Oryx 100% Fund St Katharine's Fund (including £450 earmarked for the East African Wild Life Society) £750 F. -
WILDLIFE CONSERVATION ACT 2010 2 Laws of Malaysia ACT 716
Wildlife Conservation 1 LAWS OF MALAYSIA Act 716 WILDLIFE CONSERVATION ACT 2010 2 Laws of Malaysia ACT 716 Date of Royal Assent ... ... 21 October 2010 Date of publication in the Gazette ... ... ... 4 November 2010 Publisher’s Copyright C PERCETAKAN NASIONAL MALAYSIA BERHAD All rights reserved. No part of this publication may be reproduced, stored in a retrieval system or transmitted in any form or by any means electronic, mechanical, photocopying, recording and/or otherwise without the prior permission of Percetakan Nasional Malaysia Berhad (Appointed Printer to the Government of Malaysia). Wildlife Conservation 3 LAWS OF MALAYSIA Act 716 WILDLIFE CONSERVATION ACT 2010 ARRANGEMENT OF SECTIONS PART I PRELIMINARY Section 1. Short title and commencement 2. Application 3. Interpretation PART II APPOINTMENT OF OFFICERS, ETC. 4. Appointment of officers, etc. 5. Delegation of powers 6. Power of Minister to give directions 7. Power of the Director General to issue orders 8. Carrying and use of arms PART III LICENSING PROVISIONS Chapter 1 Requirement for licence, etc. 9. Requirement for licence 10. Requirement for permit 11. Requirement for special permit 4 Laws of Malaysia ACT 716 Chapter 2 Application for licence, etc. Section 12. Application for licence, etc. 13. Additional information or document 14. Grant of licence, etc. 15. Power to impose additional conditions and to vary or revoke conditions 16. Validity of licence, etc. 17. Carrying or displaying licence, etc. 18. Change of particulars 19. Loss of licence, etc. 20. Replacement of licence, etc. 21. Assignment of licence, etc. 22. Return of licence, etc., upon expiry 23. Suspension or revocation of licence, etc. -
African Bat Conservation News
Volume 35 African Bat Conservation News August 2014 ISSN 1812-1268 © ECJ Seamark, 2009 (AfricanBats) Above: A male Cape Serotine Bat (Neoromicia capensis) caught in the Chitabi area, Okavango Delta, Botswana. Inside this issue: Research and Conservation Activities Presence of paramyxo and coronaviruses in Limpopo caves, South Africa 2 Observations, Discussions and Updates Recent changes in African Bat Taxonomy (2013-2014). Part II 3 Voucher specimen details for Bakwo Fils et al. (2014) 4 African Chiroptera Report 2014 4 Scientific contributions Documented record of Triaenops menamena (Family Hipposideridae) in the Central Highlands of 6 Madagascar Download and subscribe to African Bat Conservation News published by AfricanBats at: www.africanbats.org The views and opinions expressed in articles are no necessarily those of the editor or publisher. Articles and news items appearing in African Bat Conservation News may be reprinted, provided the author’s and newsletter refer- ence are given. African Bat Conservation News August 2014 vol. 35 2 ISSN 1812-1268 Inside this issue Continued: Recent Literature Conferences 7 Published Books / Reports 7 Papers 7 Notice Board Conferences 13 Call for Contributions 13 Research and Conservation Activities Presence of paramyxo- and coronaviruses in Limpopo caves, South Africa By Carmen Fensham Department of Microbiology and Plant Pathology, Faculty of Natural and Agricultural Sciences, University of Pretoria, 0001, Republic of South Africa. Correspondence: Prof. Wanda Markotter: [email protected] Carmen Fensham is a honours excrement are excised and used to isolate any viral RNA that student in the research group of may be present. The identity of the RNA is then determined Prof. -
Downloaded from Brill.Com09/27/2021 09:14:05PM Via Free Access 218 Rode-Margono & Nekaris – Impact of Climate and Moonlight on Javan Slow Lorises
Contributions to Zoology, 83 (4) 217-225 (2014) Impact of climate and moonlight on a venomous mammal, the Javan slow loris (Nycticebus javanicus Geoffroy, 1812) Eva Johanna Rode-Margono1, K. Anne-Isola Nekaris1, 2 1 Oxford Brookes University, Gipsy Lane, Headington, Oxford OX3 0BP, UK 2 E-mail: [email protected] Keywords: activity, environmental factors, humidity, lunarphobia, moon, predation, temperature Abstract Introduction Predation pressure, food availability, and activity may be af- To secure maintenance, survival and reproduction, fected by level of moonlight and climatic conditions. While many animals adapt their behaviour to various factors, such nocturnal mammals reduce activity at high lunar illumination to avoid predators (lunarphobia), most visually-oriented nocturnal as climate, availability of resources, competition, preda- primates and birds increase activity in bright nights (lunarphilia) tion, luminosity, habitat fragmentation, and anthropo- to improve foraging efficiency. Similarly, weather conditions may genic disturbance (Kappeler and Erkert, 2003; Beier influence activity level and foraging ability. We examined the 2006; Donati and Borgognini-Tarli, 2006). According response of Javan slow lorises (Nycticebus javanicus Geoffroy, to optimal foraging theory, animal behaviour can be seen 1812) to moonlight and temperature. We radio-tracked 12 animals as a trade-off between the risk of being preyed upon in West Java, Indonesia, over 1.5 years, resulting in over 600 hours direct observations. We collected behavioural and environmen- and the fitness gained from foraging (Charnov, 1976). tal data including lunar illumination, number of human observ- Perceived predation risk assessed through indirect cues ers, and climatic factors, and 185 camera trap nights on potential that correlate with the probability of encountering a predators. -
Nonhuman Primates
Zoological Studies 42(1): 93-105 (2003) Dental Variation among Asian Colobines (Nonhuman Primates): Phylogenetic Similarities or Functional Correspondence? Ruliang Pan1,2,* and Charles Oxnard1 1School of Anatomy and Human Biology, University of Western Australia, Crawley, Perth, WA 6009, Australia 2Institute of Zoology, Chinese Academy of Sciences, Beijing 100080, China (Accepted August 27, 2002) Ruliang Pan and Charles Oxnard (2003) Dental variation among Asian colobines (nonhuman primates): phy- logenetic similarities or functional correspondence? Zoological Studies 42(1): 93-105. In order to reveal varia- tions among Asian colobines and to test whether the resemblance in dental structure among them is mainly associated with similarities in phylogeny or functional adaptation, teeth of 184 specimens from 15 Asian colobine species were measured and studied by performing bivariate (allometry) and multivariate (principal components) analyses. Results indicate that each tooth shows a significant close relationship with body size. Low negative and positive allometric scales for incisors and molars (M2s and M3s), respectively, are each con- sidered to be related to special dental modifications for folivorous preference of colobines. Sexual dimorphism in canine eruption reported by Harvati (2000) is further considered to be associated with differences in growth trajectories (allometric pattern) between the 2 sexes. The relationships among the 6 genera of Asian colobines found greatly differ from those proposed in other studies. Four groups were detected: 1) Rhinopithecus, 2) Semnopithecus, 3) Trachypithecus, and 4) Nasalis, Pygathrix, and Presbytis. These separations were mainly determined by differences in molar structure. Molar sizes of the former 2 groups are larger than those of the latter 2 groups. -
Controlled Animals
Environment and Sustainable Resource Development Fish and Wildlife Policy Division Controlled Animals Wildlife Regulation, Schedule 5, Part 1-4: Controlled Animals Subject to the Wildlife Act, a person must not be in possession of a wildlife or controlled animal unless authorized by a permit to do so, the animal was lawfully acquired, was lawfully exported from a jurisdiction outside of Alberta and was lawfully imported into Alberta. NOTES: 1 Animals listed in this Schedule, as a general rule, are described in the left hand column by reference to common or descriptive names and in the right hand column by reference to scientific names. But, in the event of any conflict as to the kind of animals that are listed, a scientific name in the right hand column prevails over the corresponding common or descriptive name in the left hand column. 2 Also included in this Schedule is any animal that is the hybrid offspring resulting from the crossing, whether before or after the commencement of this Schedule, of 2 animals at least one of which is or was an animal of a kind that is a controlled animal by virtue of this Schedule. 3 This Schedule excludes all wildlife animals, and therefore if a wildlife animal would, but for this Note, be included in this Schedule, it is hereby excluded from being a controlled animal. Part 1 Mammals (Class Mammalia) 1. AMERICAN OPOSSUMS (Family Didelphidae) Virginia Opossum Didelphis virginiana 2. SHREWS (Family Soricidae) Long-tailed Shrews Genus Sorex Arboreal Brown-toothed Shrew Episoriculus macrurus North American Least Shrew Cryptotis parva Old World Water Shrews Genus Neomys Ussuri White-toothed Shrew Crocidura lasiura Greater White-toothed Shrew Crocidura russula Siberian Shrew Crocidura sibirica Piebald Shrew Diplomesodon pulchellum 3. -
Interim Report
Interim Report Distribution, ecology and habitat use of the Himalayan gray langur Semnopithecus ajax in Jammu and Kashmir, India. Background Himalayan gray langur, Semnopithecus ajax, is considered endangered due to its endemicity to Himalayan region and its declining population size (Groves and Molur, 2008). This primate was formerly considered a subspecies of Semnopithecus entellus (Brandon-Jones 2004, Brandon-Jones and others 2004; and Napier 1985). However, recent studies confirm its status as a species, Semnopithecus ajax (Groves 2001; Ashalakshmi 2015). Due to pre- existing confusion in taxonomy, its current distribution and conservation status are poorly understood. An assessment of (1) geographical distribution and population status, (2) conservation status, and (3) habitat use and feeding ecology are the need of the hour to develop conservation action plans for this species, across its natural range. The very first sighting record of this species was likely from Sikkim at 2700m in 1855 (Hooker 1855). Later it has been recorded in various other parts of Himalayas, e.g., in Nepal (Bishop 1975), Himachal Pradesh (Sugiyama 1976), Pakistan (Roberts 1997) and Kashmir (Lawrence 1895; Brandon-Jones 2004; Molur 2008). In this study, I propose to assess the geographical distribution, status, habitat use and feeding ecology of Himalayan gray langur in Kashmir. Kashmir (32° N, 72° E; Jammu & Kashmir state), in north western India, is an oval-shaped valley surrounded with a chain of mountains ranging from 1600m to 5000m and above. The valley has a mix of forests, orchards, croplands, and human habitation. Due to altitudinal variation, there is variation in temperature and vegetation type. -
Hipposideros Vittatus – Striped Leaf-Nosed Bat
Hipposideros vittatus – Striped leaf-nosed Bat Assessment Rationale The species is only known from the northern part of the assessment region (extent of occurrence estimated at 1,419 km2), where it occurs in Pafuri, Kruger National Park. Although it qualifies for Vulnerable D2 based on limited number of locations, there are no plausible threats. While no information exists on population size in the assessment region, it is numerous outside South Africa. Thus we assume the population is fairly large and stable in Kruger National Park. We list this species as Least Concern. Regional population effects: The subpopulations that occur in northern Kruger National Park are part of a population that is continuous across the border occurring throughout most of Zimbabwe and Mozambique. The Melissa Donnelly, iNaturalist species overall is widespread in the rest of Africa. Striped Leaf-nosed Bats have a high wing-loading (Norberg & Rayner 1987), and presumably good dispersal potential, Regional Red List status (2016) Least Concern and thus rescue effects are possible. National Red List status (2004) Not Evaluated Reasons for change Non-genuine change: Distribution New information Although fairly sparse within its distribution, this species Global Red List status (2008) Near Threatened A ranges through much of southern, Central and East Africa. The northeastern extent of its range extends from Ethiopia TOPS listing (NEMBA) (2007) None and Somalia to Kenya, Tanzania, Malawi, Zambia and CITES listing None Mozambique. It has a patchy distribution through Central Africa in the Democratic Republic of Congo, Central Endemic No African Republic, Angola, and spreads westwards to Nigeria and Guinea. The southern portion of its Sexual dimorphism is evident in this species; distribution includes Zimbabwe, Botswana, Namibia and apart from the differences in colouring, females the extreme northeastern regions of South Africa. -
Endangered Species
Not logged in Talk Contributions Create account Log in Article Talk Read Edit View history Endangered species From Wikipedia, the free encyclopedia Main page Contents For other uses, see Endangered species (disambiguation). Featured content "Endangered" redirects here. For other uses, see Endangered (disambiguation). Current events An endangered species is a species which has been categorized as likely to become Random article Conservation status extinct . Endangered (EN), as categorized by the International Union for Conservation of Donate to Wikipedia by IUCN Red List category Wikipedia store Nature (IUCN) Red List, is the second most severe conservation status for wild populations in the IUCN's schema after Critically Endangered (CR). Interaction In 2012, the IUCN Red List featured 3079 animal and 2655 plant species as endangered (EN) Help worldwide.[1] The figures for 1998 were, respectively, 1102 and 1197. About Wikipedia Community portal Many nations have laws that protect conservation-reliant species: for example, forbidding Recent changes hunting , restricting land development or creating preserves. Population numbers, trends and Contact page species' conservation status can be found in the lists of organisms by population. Tools Extinct Contents [hide] What links here Extinct (EX) (list) 1 Conservation status Related changes Extinct in the Wild (EW) (list) 2 IUCN Red List Upload file [7] Threatened Special pages 2.1 Criteria for 'Endangered (EN)' Critically Endangered (CR) (list) Permanent link 3 Endangered species in the United -
Cic Pheonotype List Caprinae©
v. 5.25.12 CIC PHEONOTYPE LIST CAPRINAE © ARGALI 1. Altai Argali Ovis ammon ammon (aka Altay Argali) 2. Khangai Argali Ovis ammon darwini (aka Hangai & Mid Altai Argali) 3. Gobi Argali Ovis ammon darwini 4. Northern Chinese Argali - extinct Ovis ammon jubata (aka Shansi & Jubata Argali) 5. Northern Tibetan Argali Ovis ammon hodgsonii (aka Gansu & Altun Shan Argali) 6. Tibetan Argali Ovis ammon hodgsonii (aka Himalaya Argali) 7. Kuruk Tagh Argali Ovis ammon adametzi (aka Kuruktag Argali) 8. Karaganda Argali Ovis ammon collium (aka Kazakhstan & Semipalatinsk Argali) 9. Sair Argali Ovis ammon sairensis 10. Dzungarian Argali Ovis ammon littledalei (aka Littledale’s Argali) 11. Tian Shan Argali Ovis ammon karelini (aka Karelini Argali) 12. Kyrgyz Argali Ovis ammon humei (aka Kashgarian & Hume’s Argali) 13. Pamir Argali Ovis ammon polii (aka Marco Polo Argali) 14. Kara Tau Argali Ovis ammon nigrimontana (aka Bukharan & Turkestan Argali) 15. Nura Tau Argali Ovis ammon severtzovi (aka Kyzyl Kum & Severtzov Argali) MOUFLON 16. Tyrrhenian Mouflon Ovis aries musimon (aka Sardinian & Corsican Mouflon) 17. Introd. European Mouflon Ovis aries musimon (aka European Mouflon) 18. Cyprus Mouflon Ovis aries ophion (aka Cyprian Mouflon) 19. Konya Mouflon Ovis gmelini anatolica (aka Anatolian & Turkish Mouflon) 20. Armenian Mouflon Ovis gmelini gmelinii (aka Transcaucasus or Asiatic Mouflon, regionally as Arak Sheep) 21. Esfahan Mouflon Ovis gmelini isphahanica (aka Isfahan Mouflon) 22. Larestan Mouflon Ovis gmelini laristanica (aka Laristan Mouflon) URIALS 23. Transcaspian Urial Ovis vignei arkal (Depending on locality aka Kopet Dagh, Ustyurt & Turkmen Urial) 24. Bukhara Urial Ovis vignei bocharensis 25. Afghan Urial Ovis vignei cycloceros 26.