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Table 7: Species Changing IUCN Red List Status (2014-2015)
IUCN Red List version 2015.4: Table 7 Last Updated: 19 November 2015 Table 7: Species changing IUCN Red List Status (2014-2015) Published listings of a species' status may change for a variety of reasons (genuine improvement or deterioration in status; new information being available that was not known at the time of the previous assessment; taxonomic changes; corrections to mistakes made in previous assessments, etc. To help Red List users interpret the changes between the Red List updates, a summary of species that have changed category between 2014 (IUCN Red List version 2014.3) and 2015 (IUCN Red List version 2015-4) and the reasons for these changes is provided in the table below. IUCN Red List Categories: EX - Extinct, EW - Extinct in the Wild, CR - Critically Endangered, EN - Endangered, VU - Vulnerable, LR/cd - Lower Risk/conservation dependent, NT - Near Threatened (includes LR/nt - Lower Risk/near threatened), DD - Data Deficient, LC - Least Concern (includes LR/lc - Lower Risk, least concern). Reasons for change: G - Genuine status change (genuine improvement or deterioration in the species' status); N - Non-genuine status change (i.e., status changes due to new information, improved knowledge of the criteria, incorrect data used previously, taxonomic revision, etc.); E - Previous listing was an Error. IUCN Red List IUCN Red Reason for Red List Scientific name Common name (2014) List (2015) change version Category Category MAMMALS Aonyx capensis African Clawless Otter LC NT N 2015-2 Ailurus fulgens Red Panda VU EN N 2015-4 -
Rediscovery of Nycticebus Coucang Insularis Robinson, 1917
Sains Malaysiana 47(10)(2018): 2533–2542 http://dx.doi.org/10.17576/jsm-2018-4710-30 Rediscovery of Nycticebus coucang insularis Robinson, 1917 (Primates: Lorisidae) at Tioman Island and its Mitochondrial Genetic Assessment (Penemuan Semula Nycticebus coucang insularis Robinson, 1917 (Primate: Lorisidae) di Pulau Tioman dan Penilaian Genetik Mitokondrianya) JEFFRINE J. ROVIE-RYAN*, MILLAWATI GANI, HAN MING GAN, GILMOORE G. BOLONGON, TAN CHENG CHENG, NORAZLINDA RAZAK, NORSYAMIMI ROSLI, MOHD AZIZOL AZIZ & KALIP MATKASIM ABSTRACT Slow lorises (Nycticebus) consist of eight species native to Southeast Asia while three species are recognised in Malaysia - N. coucang, N. menagensis and N. kayan. This study reports on the rediscovery of the subspecies N. coucang insularis Robinson, 1917 in Tioman Island and the genetic assessment of its mitochondrial DNA variation. Morphological measurements conform the specimen as the putative N. coucang but with distinct colour and markings. Two mitochondrial DNA segments (cytochrome b and control region) were produced from the subspecies representing their first registered sequences in GenBank. Genetically, the subspecies showed 99% of nucleotide similarity to N. coucang species type for both the DNA segments and constitute its own unique haplotype. Phylogenetic trees constructed using three methods (neighbour joining, maximum likelihood and Bayesian inference) showed two major groups within Nycticebus; the basal group was formed by N. pygmaeus while the second group consisted of the remaining Nycticebus species. The phylogenetic position of the subspecies, however, remains unresolved due to the observed mixing between N. coucang and N. bengalensis. Several reasons could lead to this condition including the lack of well documented voucher specimens and the short DNA fragments used. -
Molecular Data Confirm the Presence of Nycticebus Bengalensis on Langkawi Island, Malaysia
BIODIVERSITAS ISSN: 1412-033X Volume 20, Number 4, April 2019 E-ISSN: 2085-4722 Pages: 1115-1120 DOI: 10.13057/biodiv/d200424 Molecular data confirm the presence of Nycticebus bengalensis on Langkawi Island, Malaysia BADRUL MUNIR MD-ZAIN1,, KHAIRUL SYA’ADAH MOHHOYUA1, NOR RAHMAN AIFAT1, EHWAN NGADI1, NORSHAQINAH AYOB1, JEFFRINE JAPNING ROVIE-RYAN2, AHMAD AMPENG3, ABD RAHMAN MOHD-RIDWAN1,4, MARY E BLAIR5, MUHAMMAD ABU BAKAR ABDUL-LATIFF6 1School of Environmental and Natural Resource Sciences, Faculty of Science and Technology, Universiti Kebangsaan Malaysia. 43600, Bangi, Selangor, Malaysia. Tel.: +60-389-213200, email: [email protected], [email protected] 2Department of Wildlife and National Park (DWNP) Peninsular Malaysia, Km 10 Jalan Cheras, 56100 Kuala Lumpur, Malaysia 3Sarawak Forest Department, Wisma Sumber Alam Jalan Stadium, 93660 Petra Jaya, Kuching, Sarawak, Malaysia 4Centre for Pre-University Studies, Universiti Malaysia Sarawak,94300 Kota Samarahan, Sarawak, Malaysia 5Center for Biodiversity and Conservation, American Museum of Natural History, Central Park West & 79th St, New York, NY 10024, United States 6Centre of Research for Sustainable Uses of Natural Resources (CoR-SUNR), Faculty of Applied Sciences and Technology, Universiti Tun Hussein Onn Malaysia (Pagoh Campus). 84000, Muar, Johor, Malaysia Manuscript received: 23 February 2019. Revision accepted: 24 March 2019. Abstract. Md-Zain BM, Mohhoyua KS, Aifat NR, Ngadi E, Ayob N, Rovie-Ryan JJ, Ampeng A, Mohd-Ridwan AR, Blair ME, Abdul-Latiff MAB. 2019. Molecular data confirm the presence of Nycticebus bengalensis on Langkawi Island, Malaysia. Biodiversitas 20: 1115- 1120. Recent taxonomic reviews have stated the possibility of Bengal Slow Loris (Nycticebus bengalensis) presence in the Northern part of the Malay Peninsula. -
Pongo Abelii)
UvA-DARE (Digital Academic Repository) Orangutan diet: lessons from and for the wild Hardus, M.E. Publication date 2012 Link to publication Citation for published version (APA): Hardus, M. E. (2012). Orangutan diet: lessons from and for the wild. General rights It is not permitted to download or to forward/distribute the text or part of it without the consent of the author(s) and/or copyright holder(s), other than for strictly personal, individual use, unless the work is under an open content license (like Creative Commons). Disclaimer/Complaints regulations If you believe that digital publication of certain material infringes any of your rights or (privacy) interests, please let the Library know, stating your reasons. In case of a legitimate complaint, the Library will make the material inaccessible and/or remove it from the website. Please Ask the Library: https://uba.uva.nl/en/contact, or a letter to: Library of the University of Amsterdam, Secretariat, Singel 425, 1012 WP Amsterdam, The Netherlands. You will be contacted as soon as possible. UvA-DARE is a service provided by the library of the University of Amsterdam (https://dare.uva.nl) Download date:29 Sep 2021 4 Behavioral, Ecological, and Evolutionary Aspects of Meat-Eating by Sumatran Orangutans (Pongo abelii) Madeleine E. Hardus, Adriano R. Lameira, Astri Zulfa, S. Suci Utami Atmoko, Han de Vries, Serge A. Wich Abstract Meat-eating is an important aspect of human evolution, but how meat became a substantial component of the human diet is still poorly understood. Meat eating in our closest relatives, the great apes, may provide insight into the emergence of this trait, but most existing data are for chimpanzees. -
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. -
First Record of Hose's Civet Diplogale Hosei from Indonesia
First record of Hose’s Civet Diplogale hosei from Indonesia, and records of other carnivores in the Schwaner Mountains, Central Kalimantan, Indonesia Hiromitsu SAMEJIMA1 and Gono SEMIADI2 Abstract One of the least-recorded carnivores in Borneo, Hose’s Civet Diplogale hosei , was filmed twice in a logging concession, the Katingan–Seruyan Block of Sari Bumi Kusuma Corporation, in the Schwaner Mountains, upper Seruyan River catchment, Central Kalimantan. This, the first record of this species in Indonesia, is about 500 km southwest of its previously known distribution (northern Borneo: Sarawak, Sabah and Brunei). Filmed at 325The m a.s.l., IUCN these Red List records of Threatened are below Species the previously known altitudinal range (450–1,800Prionailurus m). This preliminary planiceps survey forPardofelis medium badia and large and Otter mammals, Civet Cynogalerunning 100bennettii camera-traps in 10 plots for one (Bandedyear, identified Civet Hemigalus in this concession derbyanus 17 carnivores, Arctictis including, binturong on Neofelis diardi, three Endangered Pardofe species- lis(Flat-headed marmorata Cat and Sun Bear Helarctos malayanus, Bay Cat . ) and six Vulnerable species , Binturong , Sunda Clouded Leopard , Marbled Cat Keywords Cynogale bennettii, as well, Pardofelis as Hose’s badia Civet), Prionailurus planiceps Catatan: PertamaBorneo, camera-trapping, mengenai Musang Gunung Diplogale hosei di Indonesia, serta, sustainable karnivora forest management lainnya di daerah Pegunungan Schwaner, Kalimantan Tengah Abstrak Diplogale hosei Salah satu jenis karnivora yang jarang dijumpai di Borneo, Musang Gunung, , telah terekam dua kali di daerah- konsesi hutan Blok Katingan–Seruyan- PT. Sari Bumi Kusuma, Pegunungan Schwaner, di sekitar hulu Sungai Seruya, Kalimantan Tengah. Ini merupakan catatan pertama spesies tersebut terdapat di Indonesia, sekitar 500 km dari batas sebaran yang diketa hui saat ini (Sarawak, Sabah, Brunei). -
• Thailand 18 – 30 November 2013 Phil Telfer +
x Thailand 18th ʹ 30th November 2013 Phil Telfer + Mark Bibby. A quick summary of a twelve day search for mammals in North and Central Thailand guided by Rattapon Kaichid ( known as Tu ) who together with his wife Jan runs Nature Focus Thailand, they can be very highly recommended. Many thanks to Jon Hall for their email contact which is [email protected] Tu is a really nice guy to ƚƌĂǀĞůǁŝƚŚ͕ŚĞ͛ƐĂŶĞdžĐĞůůĞŶƚĂůů-round wildlife guide and his connections help smooth the way in many of the national parks. Based on our target species, Tu and Jan put together the following itinerary: x Three days ʹ Huai Kha Khaeng wildlife sanctuary x Three days - Khao Yai national park x Four days ʹ Kaeng Krachan national park x One day ʹ Salt pans for Spoon-billed sandpiper x One day ʹ Ban Tha Kham bay for Irawaddy dolphin and Finless porpoise This was quite easy going, giving us a fair bit of time in each of the main centres. I think we did very well scoring 43 species with good views of most of these although we had no luck with any of the mega mammals such as Clouded leopard, Marbled cat, Golden cat or Sun bear which are all possibles and seen from time to time. A couple of weeks before our visit a group had seen a Golden cat catching a dove in front of one of the bird blinds. A Sun bear had been seen crossing the road one morning near the top of the mountain at Kaeng Krachan and a group that arrived there at the same time as us went on to see a Binturong an hour or so later. -
1 the Origin and Evolution of the Domestic Cat
1 The Origin and Evolution of the Domestic Cat There are approximately 40 different species of the cat family, classification Felidae (Table 1.1), all of which are descended from a leopard-like predator Pseudaelurus that existed in South-east Asia around 11 million years ago (O’Brien and Johnson, 2007). Other than the domestic cat, the most well known of the Felidae are the big cats such as lions, tigers and panthers, sub-classification Panthera. But the cat family also includes a large number of small cats, including a group commonly known as the wildcats, sub-classification Felis silvestris (Table 1.2). Physical similarity suggests that the domestic cat (Felis silvestris catus) originally derived from one or more than one of these small wildcats. DNA examination shows that it is most closely related to the African wildcat (Felis silvestris lybica), which has almost identical DNA, indicating that the African wildcat is the domestic cat’s primary ancestor (Lipinski et al., 2008). The African Wildcat The African wildcat is still in existence today and is a solitary and highly territorial animal indigenous to areas of North Africa and the Near East, the region where domestication of the cat is believed to have first taken place (Driscoll et al., 2007; Faure and Kitchener, 2009). It is primarily a nocturnal hunter that preys mainly on rodents but it will also eat insects, reptiles and other mammals including the young of small antelopes. Also known as the Arabian or North African wildcat, it is similar in appearance to a domestic tabby, with a striped grey/sandy-coloured coat, but is slightly larger and with longer legs (Fig. -
The Illegal Exploitation of the Javan Leopard (
Nature Conservation 43: 25–39 (2021) A peer-reviewed open-access journal doi: 10.3897/natureconservation.43.59399 RESEARCH ARticlE https://natureconservation.pensoft.net Launched to accelerate biodiversity conservation The illegal exploitation of the Javan Leopard (Panthera pardus melas) and Sunda Clouded Leopard (Neofelis diardi) in Indonesia Lalita Gomez1,2, Chris R. Shepherd1 1 Monitor Conservation Research Society, Big Lake, Canada 2 Oxford Wildlife Trade Research Group, Oxford Brookes University, Oxford, UK Corresponding author: Chris R. Shepherd ([email protected]) Academic editor: M. Auliya | Received 6 October 2020 | Accepted 15 January 2021 | Published 22 March 2021 http://zoobank.org/17D9AAB6-8A94-4B5A-932F-6633FAD5D42B Citation: Gomez L, Shepherd CR (2021) The illegal exploitation of the Javan Leopard (Panthera pardus melas) and Sunda Clouded Leopard (Neofelis diardi) in Indonesia. Nature Conservation 43: 25–39. https://doi.org/10.3897/ natureconservation.43.59399 Abstract Indonesia is home to the Javan Leopard (Panthera pardus melas) and the Sunda Clouded Leopard (Neofelis diardi), both of which are threatened by habitat loss, human-wildlife conflict issues and the illegal wildlife trade. Leopards and clouded leopards are threatened by the illegal wildlife trade across their range, how- ever, very little is known of the illegal trade in these two species in Indonesia, or of the efforts made to tackle this crime. Both the Javan Leopard and Sunda Clouded Leopard are protected species in Indonesia and both species are listed in Appendix I of the Convention on International Trade in Endangered Species of Wild Fauna and Flora (CITES), meaning commercial international trade is generally prohibited. To better understand the trade, and efforts to end this trade, we collected records of seizures and prosecutions relating to Javan Leopards and Sunda Clouded Leopards in Indonesia for the period 2011–2019. -
The Clouded Leopard in Malaysian Borneo
The clouded leopard in Malaysian Borneo Alan Rabinowitz, Patrick Andau and Paul P. K. Chai The clouded leopard Neofelis nebulosa has already disappeared from part of its range in southern Asia; it is classified as vulnerable by IUCN and is on Appendix I of CITES. Little is known about this secretive forest-dweller anywhere in its range, and the sparse information needs to be augmented so that effective conservation measures may be taken if necessary. In early 1986 the senior author travelled through the interior of Malaysian Borneo, staying at villages and timber camps, to assess the status of the species in the region and to find out more about its behaviour. Clouded leopard in captivity in Thailand (Alan Rabinowitz). Clouded leopard in Malaysian Borneo 107 Downloaded from https://www.cambridge.org/core. IP address: 170.106.40.40, on 29 Sep 2021 at 10:57:47, subject to the Cambridge Core terms of use, available at https://www.cambridge.org/core/terms. https://doi.org/10.1017/S0030605300026648 The clouded leopard is one of the most elusive of the larger felids in Asian forests. With body characteristics that fall between those of large and small cats, it has upper canines that are relatively longer than in any other living felid (Guggisberg, 1975). These tusk-like canines have a sharp posterior edge, which caused Sterndale (1884) to compare the clouded leopard to the extinct sabre-toothed tiger. Occurring over an extensive area of southern Asia, the clouded leopard is the largest wild felid on the island of Borneo. Due to its secretive and solitary habits, however, this cat is seldom observed, and much of the knowledge con- cerning its ecology remains anecdotal. -
Slow Loris Forest Protector Teacher's Pack
2 www.nocturama.org https://www.facebook.com/pages/Little-Fireface-Project/ littlefi[email protected] INTRODUCTION Welcome! Welcome to the Slow Loris—Forest Protector’s Teacher’s Pack and Learning Exercise Book. The purpose of this short booklet is to explain how to use the book and to help to reinforce its message through a series of fun and easy-to- We at the Little Fireface Project (LFP) our so glad you are using this teacher’s use exercises. pack. First we want to tell you about ourselves and our passion about one of the world’s most unique little primates. LFP is a UK Charity based out of Ox- ford Brookes University set up to help save the slow loris through studying In this pack, you will find the following materials to help you and your students them in the wild and through education projects. explore the story of two night-active (nocturnal) primates, slow lorises: a moth- er (Tereh—speedy) and her young son (Bunga—flower). Tereh lovingly teaches Why the slow loris and why a charity dedicated to one group of animals? Well, her son the life skills he needs to be a grown-up slow loris. At the same time, the eight species of slow lorises, found only in Asia, are facing a tough time. Bunga learns that by doing his job in the forest, he helps the forest to grow, They are threatened for many reasons beyond the habitat loss causing many of while helping protect the crops grown by people. Asia’s species to go extinct. -
PICA Project Report (Action A2.2 & 2.3)
PICA Project Report (Action A2.2 & 2.3) Investigation of Pallas’s cat activity patterns and temporal interactions with sympatric species Authors: Katarzyna Ruta, Gustaf Samelius, David Barclay, Emma Nygren PICA - “Conservation of the Pallas’s cat through capacity building, research, and global planning” 1. Introduction: 1.1 Activity patterns of wild felids: Activity patterns form a part of species’ adaptation to their environment (Beltran & Delibes, 1994) and are therefore a fundamental aspect of animal behaviour (Nielsen, 1983; Weller & Bennett, 2001). Felids are generally considered to be crepuscular and nocturnal in their activity (Kitchener, 1991), although they are well adapted to function in a wide range of light conditions (Sunquist & Sunquist, 2002). Numerous abiotic pressures and biotic interactions are known to shape the temporal behaviour of (cat-like) carnivores (Marinho et al., 2018), including changes in temperature (Beltran & Delibes, 1994; Podolski et al., 2013), light (Huck et al., 2017; Heurich et al., 2014) and season (Podolski et al., 2013; Manfredi et al., 2011), sex and reproductive status of the animal (Kolbe & Squires, 2007; Schmidt, 1999; Schmidt et al., 2009), predation risk (Caro, 2005; Farías et al., 2012) and human disturbance (Wolf & Ale, 2009; Ale & Brown, 2009). Owing to the dietary constraints of carnivores whose preys have their own well-defined circadian rhythms (Halle, 2000; Zielinski, 2000), the availability and vulnerability of prey is, however, considered as one of the main influences on predator temporal activity (Zielinski, 1988; Lodé, 1995). According to Optimal Foraging Theory, predators are expected to synchronize their daily activity with the activity of their most profitable prey, increasing the probability of encounters while reducing energy expenditure (MacArthur & Pianka, 1966; Monterroso et al., 2013; Emmons, 1987).