Northern Rivers Feral Deer Identification Guide
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
About Pigs [PDF]
May 2015 About Pigs Pigs are highly intelligent, social animals, displaying elaborate maternal, communicative, and affiliative behavior. Wild and feral pigs inhabit wide tracts of the southern and mid-western United States, where they thrive in a variety of habitats. They form matriarchal social groups, sleep in communal nests, and maintain close family bonds into adulthood. Science has helped shed light on the depths of the remarkable cognitive abilities of pigs, and fosters a greater appreciation for these often maligned and misunderstood animals. Background Pigs—also called swine or hogs—belong to the Suidae family1 and along with cattle, sheep, goats, camels, deer, giraffes, and hippopotamuses, are part of the order Artiodactyla, or even-toed ungulates.2 Domesticated pigs are descendants of the wild boar (Sus scrofa),3,4 which originally ranged through North Africa, Asia and Europe.5 Pigs were first domesticated approximately 9,000 years ago.6 The wild boar became extinct in Britain in the 17th century as a result of hunting and habitat destruction, but they have since been reintroduced.7,8 Feral pigs (domesticated animals who have returned to a wild state) are now found worldwide in temperate and tropical regions such as Australia, New Zealand, and Indonesia and on island nations, 9 such as Hawaii.10 True wild pigs are not native to the New World.11 When Christopher Columbus landed in Cuba in 1493, he brought the first domestic pigs—pigs who subsequently spread throughout the Spanish West Indies (Caribbean).12 In 1539, Spanish explorers brought pigs to the mainland when they settled in Florida. -
Water Consumption by Rusa Deer (Cervus Timorensis) Stags As Infl Uenced by Different Types of Food
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by University of Queensland eSpace Animal Science 2005, 80: 83-88 Water intake of rusa stags in Australia 1357-7298/04/40500083$20.00 © 2005 British Society of Animal Science Water consumption by rusa deer (Cervus timorensis) stags as infl uenced by different types of food W. Yape Kii and G. McL. Dryden† School of Animal Studies, University of Queensland, Gatton, Queensland 4345, Australia †Email : [email protected] Abstract During winter in southern Queensland, eight rusa deer stags aged 4 years were given ad libitum lucerne (Medicago sativa) hay and confi ned in individual metabolism pens for 26 days. Stags ate 2·04 kg dry matter (DM) per day and drank 6·4 kg water per day, while the drinking water : food DM ratio was 3·3 l/kg. In experiment 2, seven rusa stags were given ad libitum lucerne hay or oaten (Avena spp. ) hay with or without barley grain supplementation (200 g/day) for 56 days (four periods). This experiment was conducted from 26 July to 19 September 2001, when the stags were exhibiting the behaviour characteristic of the rut. Rusa stags ate 1·19 and 1·17 kg DM per day of lucerne and oaten hay respectively. Rusa stags given oaten hay drank slightly more water than those that received lucerne hay (5·34 and 4·47 kg/day, respectively). The drinking water : food DM ratios were 3·81 and 4·67 kg/kg for lucerne and oaten hay, respectively. -
Spread Oaks White-Tailed Deer and Wild Pig Opportunities
Spread Oaks White-tailed Deer and Wild Pig Opportunities Welcome to the great outdoors at Spread Oaks Ranch! We have a typical mid-latitude fall/winter, meaning our weather can vary from hot to cold, dry to wet. You’ll hunt along the Colorado River floodplain and its river bottom hardwoods and savannahs that provide a remarkably scenic backdrop to your hunt from one of our deer and pig blinds. In addition to a morning waterfowl hunt, your Spread Oaks Lodge hunting season package includes an afternoon hunt with the option to take one doe and an unlimited numbers of wild pigs and coyotes. Costs. The opportunity to shoot a doe at the ranch is part of the hunting season package. All whitetail bucks 130” or less are priced at $500. If rack is >130” we use standard high fence pricing: 131 to 139” @ $2,000; 140 to 149” @ $3,500; 150 to 159” @ $5,000; 160 to 169” @ $5,500; 170 to 179” @ $6,500; 180 to 189” @ $7,500; 190 to 199” @ $8,500; racks greater than 200” priced at $10,000. Pricing for bucks is the same for both river bottom “low fence” and high fence deer. Our $100 guide fee is designed for safety and to ensure that the “right” deer are harvested, however, experienced hunters can elect not to use a guide for either deer or hog. Staff will help you decide who, if any, in your group will need a guide. If you wish to take your harvest with you, all you need is a cooler and we’ll handle the rest. -
An Analysis of the Phylogenetic Relationship of Thai Cervids Inferred from Nucleotide Sequences of Protein Kinase C Iota (PRKCI) Intron
Kasetsart J. (Nat. Sci.) 43 : 709 - 719 (2009) An Analysis of the Phylogenetic Relationship of Thai Cervids Inferred from Nucleotide Sequences of Protein Kinase C Iota (PRKCI) Intron Kanita Ouithavon1, Naris Bhumpakphan2, Jessada Denduangboripant3, Boripat Siriaroonrat4 and Savitr Trakulnaleamsai5* ABSTRACT The phylogenetic relationship of five Thai cervid species (n=21) and four spotted deer (Axis axis, n=4), was determined based on nucleotide sequences of the intron region of the protein kinase C iota (PRKCI) gene. Blood samples were collected from seven captive breeding centers in Thailand from which whole genomic DNA was extracted. Intron1 sequences of the PRKCI nuclear gene were amplified by a polymerase chain reaction, using L748 and U26 primers. Approximately 552 base pairs of all amplified fragments were analyzed using the neighbor-joining distance matrix method, and 19 parsimony- informative sites were analyzed using the maximum parsimony approach. Phylogenetic analyses using the subfamily Muntiacinae as outgroups for tree rooting indicated similar topologies for both phylogenetic trees, clearly showing a separation of three distinct genera of Thai cervids: Muntiacus, Cervus, and Axis. The study also found that a phylogenetic relationship within the genus Axis would be monophyletic if both spotted deer and hog deer were included. Hog deer have been conventionally classified in the genus Cervus (Cervus porcinus), but this finding supports a recommendation to reclassify hog deer in the genus Axis. Key words: Thailand, the family Cervidae, protein kinase C iota (PRKCI) intron, phylogenetic tree, taxonomy INTRODUCTION 1987; Gentry, 1994). Cervids, or what is commonly called “deer,” are mostly characterized The family Cervidae is one of the most by antlers with a bony inner core and velvet skin specious families of artiodactyls, with an extensive cover. -
Sus Celebensis Muller and Schlegel 1843) in TANJUNG PEROPA WILDLIFE RESERVE, SOUTHEAST SULAWESI
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Media Konservasi Media Konservasi Vol. 13, No. 2 Agustus 2008 : 90 – 93 DEMOGRAPHIC PARAMETERS AND BEHAVIOURS OF SULAWESI WARTY PIG (Sus celebensis Muller and Schlegel 1843) IN TANJUNG PEROPA WILDLIFE RESERVE, SOUTHEAST SULAWESI 1 1 2, 3 1 M. JAMALUDIN , A. H. MUSTARI , J.A. BURTON , J. B. HERNOWO 1 Department of Forest Resources Conservation and Ecotourism, Faculty of Forestry, Bogor Agricultural University. 2VBS, Royal (Dick) School of Veterinary Studies, The University of Edinburgh, EH9 1QH, Scotland, UK. 3CRC, Royal Zoological Society of Antwerp, Koningin Astridplein 26, 2018 Antwerp, Belgium. Diterima 20 Pebruari 2008/Disetujui 30 April 2008 ABSTRACT Studi ini bertujuan untuk mengetahui kepadatan populasi, ukuran populasi, struktur umur, jumlah anak per kelahiran (litter size) dan perilaku babi hutan sulawesi (warty pig) di Suaka Margasatwa Tanjung Peropa di Sulawesi Tenggara. Hasil penelitian menunjukkan bahwa kepadatan populasi babi hutan sulawesi di suaka margasatwa mencapai 43 individu per km2 berarti jumlah populasi total diperkirakan sebanyak 13.594 individu (dalam area berhutan seluas 389,37 km2). Di bagian selatan suaka margasatwa dimana studi ini dilaksanakan secara invensif, didapatkan jumlah individu menurut struktur umur berturut-turut untuk bayi, muda, dewasa dan tua adalah 34, 29, 23 dan 2 individu. Seks rasio 1 : 1,44 untuk populasi total dan 1:1,25 untuk populasi reproduktif, dan litter size adalah 1-3 bayi. Kategori perilaku yang diamati terdiri dari mencari makan, berkubang dan istirahat. Sedangkan perilaku sosial babi hutan sulawesi yang ditemukan terdiri dari perilaku makan, berkubang, aktivitas seksual dan penghindaran predator. -
Shells and Ochre in Middle Paleolithic Qafzeh Cave, Israel: Indications for Modern Behavior
Journal of Human Evolution 56 (2009) 307–314 Contents lists available at ScienceDirect Journal of Human Evolution journal homepage: www.elsevier.com/locate/jhevol Shells and ochre in Middle Paleolithic Qafzeh Cave, Israel: indications for modern behavior Daniella E. Bar-Yosef Mayer a,*, Bernard Vandermeersch b, Ofer Bar-Yosef c a The Leon Recanati Institute for Maritime Studies and Department of Maritime Civilizations, University of Haifa, Haifa 31905, Israel b Laboratoire d’Anthropologie des Populations du Passe´, Universite´ Bordeaux 1, Bordeaux, France c Department of Anthropology, Harvard University, Cambridge MA 02138, USA article info abstract Article history: Qafzeh Cave, the burial grounds of several anatomically modern humans, producers of Mousterian Received 7 March 2008 industry, yielded archaeological evidence reflecting their modern behavior. Dated to 92 ka BP, the lower Accepted 15 October 2008 layers at the site contained a series of hearths, several human graves, flint artifacts, animal bones, a collection of sea shells, lumps of red ochre, and an incised cortical flake. The marine shells were Keywords: recovered from layers earlier than most of the graves except for one burial. The shells were collected and Shell beads brought from the Mediterranean Sea shore some 35 km away, and are complete Glycymeris bivalves, Modern humans naturally perforated. Several valves bear traces of having been strung, and a few had ochre stains on Glycymeris insubrica them. Ó 2008 Elsevier Ltd. All rights reserved. Introduction and electron spin resonance (ESR) readings that placed both the Skhul and Qafzeh hominins in the range of 130–90 ka BP (Schwarcz Until a few years ago it was assumed that seashells were et al., 1988; Valladas et al., 1988; Mercier et al., 1993). -
MALE GENITAL ORGANS and ACCESSORY GLANDS of the LESSER MOUSE DEER, TRAGULUS Fa VAN/CUS
MALE GENITAL ORGANS AND ACCESSORY GLANDS OF THE LESSER MOUSE DEER, TRAGULUS fA VAN/CUS M. K. VIDYADARAN, R. S. K. SHARMA, S. SUMITA, I. ZULKIFLI, AND A. RAZEEM-MAZLAN Faculty of Biomedical and Health Science, Universiti Putra Malaysia, 43400 UPM Serdang, Selangor, Malaysia (MKV), Faculty of Veterinary Medicine and Animal Sciences, Universiti Putra Malaysia, 43400 UPM Serdang, Selangor, Malaysia (RSKS, SS, /Z), Downloaded from https://academic.oup.com/jmammal/article/80/1/199/844673 by guest on 01 October 2021 Department of Wildlife and National Parks, Zoo Melaka, 75450 Melaka, Malaysia (ARM) Gross anatomical features of the male genital organs and accessory genital glands of the lesser mouse deer (Tragulus javanicus) are described. The long fibroelastic penis lacks a prominent glans and is coiled at its free end to form two and one-half turns. Near the tight coils of the penis, on the right ventrolateral aspect, lies a V-shaped ventral process. The scrotum is prominent, unpigmented, and devoid of hair and is attached close to the body, high in the perineal region. The ovoid, obliquely oriented testes carry a large cauda and caput epididymis. Accessory genital glands consist of paired, lobulated, club-shaped vesic ular glands, and a pair of ovoid bulbourethral glands. A well-defined prostate gland was not observed on the surface of the pelvic urethra. Many features of the male genital organs of T. javanicus are pleisomorphic, being retained from suiod ancestors of the Artiodactyla. Key words: Tragulus javanicus, male genital organs, accessory genital glands, reproduc tion, anatomy, Malaysia The lesser mouse deer (Tragulus javan gulidae, and Bovidae (Webb and Taylor, icus), although a ruminant, possesses cer 1980). -
The Phylogenetic Roots of Human Lethal Violence José María Gómez1,2, Miguel Verdú3, Adela González-Megías4 & Marcos Méndez5
LETTER doi:10.1038/nature19758 The phylogenetic roots of human lethal violence José María Gómez1,2, Miguel Verdú3, Adela González-Megías4 & Marcos Méndez5 The psychological, sociological and evolutionary roots of 600 human populations, ranging from the Palaeolithic era to the present conspecific violence in humans are still debated, despite attracting (Supplementary Information section 9c). The level of lethal violence the attention of intellectuals for over two millennia1–11. Here we was defined as the probability of dying from intraspecific violence propose a conceptual approach towards understanding these roots compared to all other causes. More specifically, we calculated the level based on the assumption that aggression in mammals, including of lethal violence as the percentage, with respect to all documented humans, has a significant phylogenetic component. By compiling sources of mortality, of total deaths due to conspecifics (these sources of mortality from a comprehensive sample of mammals, were infanticide, cannibalism, inter-group aggression and any other we assessed the percentage of deaths due to conspecifics and, type of intraspecific killings in non-human mammals; war, homicide, using phylogenetic comparative tools, predicted this value for infanticide, execution, and any other kind of intentional conspecific humans. The proportion of human deaths phylogenetically killing in humans). predicted to be caused by interpersonal violence stood at 2%. Lethal violence is reported for almost 40% of the studied mammal This value was similar to the one phylogenetically inferred for species (Supplementary Information section 9a). This is probably the evolutionary ancestor of primates and apes, indicating that a an underestimation, because information is not available for many certain level of lethal violence arises owing to our position within species. -
Evolution of Sambar As Prey of Tiger, Leopard, Wild Dog & Man
Secrets of the Sambar - Vol 3. Evolution of Sambar As Prey of Tiger, Leopard, Wild Dog & Man Sambar have co-evolved as the favourite prey of the tiger for at least twelve thousand years. So it is not surprising that wildlife biologist Dr. A. J. T. Johnsingh tells his students and trainee forest officers that in the hilly areas of India, ‘sambar conservation is tiger conservation’ for sambar are biologically, behaviourally and ecologically adapted to be the best prey of tiger. Dr A. J. T. Johnsingh t is commonly stated by hunters and wildlife Right: The stalk and subsequent pursuit illustrated biologists that sambar are an incredibly elusive on the following pages culminated with the tigress and wary creature whose senses have been delivering one powerful bite, crushing the calves I cervical vertebrae and windpipe. The calf emitted honed to a keen edge as the direct result of having evolved as prey of the tiger. This statement implies a shrieking wail and instantly death was upon it. that sambar evolved through the process of natural As Forest Officer Gobind Sagar Bhardwaj was selection or what is often referred to as ‘survival busy photographing every moment of this once in of the fittest’. That is, those who were best adapted a lifetime wild action, his heart was thumping and to their environment survived to reproduce and he was gushing with adrenalin fueled excitement. pass on their genes to their offspring, and the best adapted offspring survived and passed on their However, tigers do not seem to single out the genes to their offspring and so forth. -
Zoologische Mededelingen Uitgegeven Door Het
ZOOLOGISCHE MEDEDELINGEN UITGEGEVEN DOOR HET RIJKSMUSEUM VAN NATUURLIJKE HISTORIE TE LEIDEN (MINISTERIE VAN CULTUUR, RECREATIE EN MAATSCHAPPELIJK WERK) Deel 45 no. 7 15 Februari 1971 ON THE IDENTITY OF CERVUS NIGRICANS BROOKE, 1877, WITH REMARKS UPON OTHER DEER FROM THE PHILIPPINES by L. J. DOBRORUKA Zoological Garden, Prague With 2 text-figures and 3 plates A great number of papers deal with the deer of the Philippine Islands but in spite of this fact the taxonomy and the nomenclature are still not clear. The first author who recapitulated all known facts about the Philippine deer was Brooke (1877), who also described a new species, Cervus nigricans. The description is exact, with figures of the habitus and the skull of the indicated holotype (♀), and in my opinion Haltenorth (1963) had no reason to con- sider C. nigricans a nomen nudum. The validity of the name Cervus nigricans is in full agreement with the International Code of Zoological Nomenclature, adopted by the XVth International Congress of Zoology. Cervus nigricans is rather rare in the collections of museums and, there- fore, I am much obliged to Dr. A. M. Husson for allowing me to examine the material of the Rijksmuseum van Natuurlijke Historie in Leiden. The material of this museum was mentioned already in Brooke's paper (1877:59) and is therefore most valuable for a study of this species, apart from the type material, of course. At the present time the following material of this species is available in the Leiden Museum: No. 19605 ♂ — mounted specimen and skull from Manila, Philippines. Presented by M. -
Handraising Exotic Animals Western Plains
HANDRAISING EXOTIC ANIMALS WESTERN PLAINS ZOO GENERAL DIRECTIVES: * All neonates (newborn) to be given colostrum for the first 24 - 36 hours where possible. Bovids, cervids, camelids, hippos etc. (order: Artiodactyla) to receive bovine colostrum. Equids, tapir, rhinos etc. (order: Perissodactyla) to receive equine colostrum. * All milk formulas to be gradually increased to 100% strength concentrations as recommended. i.e. Commence at 25% - 50% concentrations supplemented with vytrate, staged up by 25% at 24 hour intervals until 100% is reached. Use pre-boilded water to make up formulas. * Young to be fed 12 - 20% of their bodyweight in milk formula each day, divided equally between feeds. If innadequate volumes of formula are suckled then the neonate is to be tube fed until intake is adequate from the bottle. * Number of feeds per day is determined by species. * Weigh initially and weight gain/loss to be monitored at least weekly. * Routine is extremely important. Feeding times must be set and adhered to. It is usually better for one person to initiate feeding and to introduce other feeders as soon as possible to avoid neonates imprinting on one person. * All young need to be stimulated to urinate and defaecate after each feed by gentle patting - never rub. Ensure they are left clean afterwards. * Hygiene is of great importance. Bottles and teats need to be washed thoroughly and soaked in sterilising solution (Halasept). Utensils are to be rinsed with pre-boiled water before use. Face wipes are not shared with anus wipes etc. Cloths to be washed daily. All young to be left with a clean mouth after the feed (includes chin, lips etc.) * Milk temperature is to be fed at body temperature. -
Sexual Selection and Extinction in Deer Saloume Bazyan
Sexual selection and extinction in deer Saloume Bazyan Degree project in biology, Master of science (2 years), 2013 Examensarbete i biologi 30 hp till masterexamen, 2013 Biology Education Centre and Ecology and Genetics, Uppsala University Supervisor: Jacob Höglund External opponent: Masahito Tsuboi Content Abstract..............................................................................................................................................II Introduction..........................................................................................................................................1 Sexual selection........................................................................................................................1 − Male-male competition...................................................................................................2 − Female choice.................................................................................................................2 − Sexual conflict.................................................................................................................3 Secondary sexual trait and mating system. .............................................................................3 Intensity of sexual selection......................................................................................................5 Goal and scope.....................................................................................................................................6 Methods................................................................................................................................................8