Diamond Python Morelia Spilota Spilota
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Problems of Python Classification and Hybrid Pythons
PROBLEMS OF PYTHON CLASSIFICATION AND HYBRID PYTHONS. By: Raymond Hoser, 170 Lawson Street, Redfern, NSW, 2016, Australia. Contents: Introduction - Summary of the problems in classifying Australia's pythons - Hybrids between species - Acknowledge ments - References. INTRODUCTION Australasia's pythons attract disproportionate in terest from herpetologists within Australia and elsewhere. There is also considerable debate in relation to the relationships between species, with various arrangements being proposed. Authors including Cogger (1986), Schmida (1985), and Stafford (1986), have tended to follow 'con sensus opinion' when assigning generic names to Australasian pythons. References in relation to general and more specific aspects of Australian pythons can be found in Haser (1981 a , 1981 b, 1981 c and 1982), and elsewhere. This short paper gives a summary of the problems facing Australian python taxonomists and gives details of an unusual captive breeding that resulted in hybrids between species being produced. SUMMARY OF THE PROBLEMS IN CLASSIFYING AUSTRALIA'S PYTHONS With the exception of the Black headed python and Woma (Genus Aspidites), all other Australian py thons have at various times been assigned to a number of different genera. Numerous schemes of 134 classification for the rema1n1ng Australian spe cies of python have been proposed. These include Hoser (1982), McDowell (1975), and Stull (1935). The schemes range from the placing of all species in the genus Python shared with other non Austra lian species, to placing the species in question in up to seven genera. Namely Bot"h:PochiZus3 Chon dropython3 Liasis3 LisaZia3 Liasis3 MoreZia3 and Python. The assignment of given species within a particular genus is also a matter of conflict. -
Broad-Headed Snake (Hoplocephalus Bungaroides)', Proceedings of the Royal Zoological Society of New South Wales (1946-7), Pp
Husbandry Guidelines Broad-Headed Snake Hoplocephalus bungaroides Compiler – Charles Morris Western Sydney Institute of TAFE, Richmond Captive Animals Certificate III RUV3020R Lecturers: Graeme Phipps, Jacki Salkeld & Brad Walker 2009 1 Occupational Health and Safety WARNING This Snake is DANGEROUSLY VENOMOUS CAPABLE OF INFLICTING A POTENTIALLY FATAL BITE ALWAYS HAVE A COMPRESSION BANDAGE WITHIN REACH SNAKE BITE TREATMENT: Do NOT wash the wound. Do NOT cut the wound, apply substances to the wound or use a tourniquet. Do NOT remove jeans or shirt as any movement will assist the venom to enter the blood stream. KEEP THE VICTIM STILL. 1. Apply a broad pressure bandage over the bite site as soon as possible. 2. Keep the limb still. The bandage should be as tight as you would bind a sprained ankle. 3. Extend the bandage down to the fingers or toes then up the leg as high as possible. (For a bite on the hand or forearm bind up to the elbow). 4. Apply a splint if possible, to immobilise the limb. 5. Bind it firmly to as much of the limb as possible. (Use a sling for an arm injury). Bring transport to the victim where possible or carry them to transportation. Transport the victim to the nearest hospital. Please Print this page off and put it up on the wall in your snake room. 2 There is some serious occupational health risks involved in keeping venomous snakes. All risk can be eliminated if kept clean and in the correct lockable enclosures with only the risk of handling left in play. -
Investigations Into the Presence of Nidoviruses in Pythons Silvia Blahak1, Maria Jenckel2,3, Dirk Höper2, Martin Beer2, Bernd Hoffmann2 and Kore Schlottau2*
Blahak et al. Virology Journal (2020) 17:6 https://doi.org/10.1186/s12985-020-1279-5 RESEARCH Open Access Investigations into the presence of nidoviruses in pythons Silvia Blahak1, Maria Jenckel2,3, Dirk Höper2, Martin Beer2, Bernd Hoffmann2 and Kore Schlottau2* Abstract Background: Pneumonia and stomatitis represent severe and often fatal diseases in different captive snakes. Apart from bacterial infections, paramyxo-, adeno-, reo- and arenaviruses cause these diseases. In 2014, new viruses emerged as the cause of pneumonia in pythons. In a few publications, nidoviruses have been reported in association with pneumonia in ball pythons and a tiger python. The viruses were found using new sequencing methods from the organ tissue of dead animals. Methods: Severe pneumonia and stomatitis resulted in a high mortality rate in a captive breeding collection of green tree pythons. Unbiased deep sequencing lead to the detection of nidoviral sequences. A developed RT-qPCR was used to confirm the metagenome results and to determine the importance of this virus. A total of 1554 different boid snakes, including animals suffering from respiratory diseases as well as healthy controls, were screened for nidoviruses. Furthermore, in addition to two full-length sequences, partial sequences were generated from different snake species. Results: The assembled full-length snake nidovirus genomes share only an overall genome sequence identity of less than 66.9% to other published snake nidoviruses and new partial sequences vary between 99.89 and 79.4%. Highest viral loads were detected in lung samples. The snake nidovirus was not only present in diseased animals, but also in snakes showing no typical clinical signs. -
Carpet Python Morelia Spilota (Lacépède, 1804) Including Undisturbed Remnant Bushland Near Perth and the Darling Size Ranges, Yanchep National Park, and Garden Island
Carpet Python Morelia spilota (Lacépède, 1804) including undisturbed remnant bushland near Perth and the Darling Size Ranges, Yanchep National Park, and Garden Island. Populations also occur on St Francis Island (South Australia), and islands of the Averages 2.0 m total length, though individuals have been reported Archipelago of the Recherche (Western Australia). to 4.0 m in length. Morelia spilota variegata Weight Distributed across South Australia, Victoria, inland NSW, Morelia spilota imbricata Queensland, Northern Territory, and the Kimberley region of Western Australia. Males For further information regarding the distribution of this species Up to 1.1 kg please refer to www.naturemap.dec.wa.gov.au Females Up to 4.5 kg Habitat Subspecies Photo: Babs & Bert Wells/DEC Morelia spilota variegata Occurs in mesic (areas with moderate amounts of moisture) to semi- Three subspecies are currently recognised: arid habitats, from the Kimberley region to northern Victoria. • Morelia spilota imbricata (southern Western Australia and eastern South Australia) Morelia spilota imbricata • Morelia spilota spilota (eastern NSW and lowland New Guinea) This subspecies has been recorded in semi-arid coastal and inland habitats consisting of Banksia woodland, eucalypt woodlands, and • Morelia spilota variegata (remainder of range including northern grasslands. Western Australia) Behaviour Description In the summer months, the Carpet Python is active either at night, or Colour patterns vary across their geographic range. In Western at dawn and dusk. In cooler months it may be active during the Australia, the colour varies from pale to dark brown, with blackish daytime and occasionally has been seen to bask in the sun on cool blotches or variegations, which may form cross bands. -
Population Ecology of a Cryptic Arboreal Snake (Hoplocephalus Bitorquatus)
CSIRO PUBLISHING Australian Journal of Zoology https://doi.org/10.1071/ZO18009 Population ecology of a cryptic arboreal snake (Hoplocephalus bitorquatus) Michael B. Shelton A,C, Ross L. Goldingay A and Stephen S. Phillips B ASchool of Environment, Science and Engineering, Southern Cross University, Lismore, NSW 2480, Australia. BBiolink Ecological Consultants, 9 Marshall Street, Uki, NSW 2484, Australia. CCorresponding author. Email: [email protected] Abstract. Biologists have traditionally been reluctant to study arboreal snakes due to low rates of capture. Overlooking such taxa can mislead interpretations of population trends for data-deficient species. We used regularly spaced transect searches and standard capture–mark–recapture techniques to describe population structure, growth rates, survival and capture probability in a population of the pale-headed snake (Hoplocephalus bitorquatus) in southern Queensland. We obtained data from 194 captures of 113 individual snakes between 2009 and 2015. Using the Cormack–Jolly–Seber method, we estimated apparent annual survival in subadult snakes at 0.23 Æ 0.01 (s.e.) and 0.81 Æ 0.08 for adults. Capture probability was estimated at 0.16 Æ 0.14 per session in subadult snakes and 0.33 Æ 0.06 for adults. Within the red gum forests of our study site, we estimate pale-headed snake density at ~13 Æ 7ha–1. Using von Bertalanffy growth modelling, we predict that snakes reach sexual maturity after about four years and may live for up to 20. Our results suggest that the species is a ‘k’ strategist, characterised by slow maturation and low fecundity. These traits suggest that populations will recover slowly following decline, exacerbating the risk of local extinction. -
Spatial Ecology of a Threatened Python (Morelia Spilota Imbricata) and the Effects of Anthropogenic Habitat Change
Austral Ecology (2005) 30, 261–274 Spatial ecology of a threatened python (Morelia spilota imbricata) and the effects of anthropogenic habitat change D. PEARSON,1 R. SHINE2* AND A. WILLIAMS1 1Department of Conservation and Land Management, Wanneroo, Western Australia, Australia and 2School of Biological Sciences A08, University of Sydney, Sydney, New South Wales 2006, Australia (Email: [email protected]) Abstract Large predators play important ecological roles, but often are sensitive to habitat changes and thus are early casualties of habitat perturbation. Pythons are among the largest predators in many Australian environments, and hence warrant conservation-orientated research. Carpet pythons (Morelia spilota imbricata) have declined across much of south-western Australia presumably because of habitat clearance and degradation. Information on habitat use, home range sizes and movements is needed to plan for the conservation of this important predator. We studied pythons at two study sites (Garden Island and Dryandra Woodland) with markedly different climates, habitat types and disturbance histories. We surgically implanted radio-transmitters in 91 pythons and tracked them for periods of 1 month to 4 years. Dryandra pythons remained inactive inside tree hollows during cooler months (May–September), whereas some (especially small) pythons on Garden Island continued to move and feed. Overall weekly displacements (mean = 100–150 m) were similar at the two study sites and among sex/ age classes, except that reproductive females were sedentary during summer while they were incubating eggs. Home ranges averaged 15–20 ha. Adult male pythons had larger home ranges than adult females at Dryandra, but not at Garden Island. Radio-tracked snakes at Dryandra exhibited high site fidelity, returning to previously occupied logs after long absences and reusing tree hollows for winter shelter. -
Inclusion Body Disease in Australian Snakes Jun 2013
Inclusion body disease in Australian snakes Fact sheet Introductory statement Inclusion body disease (IBD) is an important disease of snakes because of its 100% mortality rate and lack of definite knowledge regarding epidemiology, diagnosis, treatment and prevention. While IBD appears to be present in captive Australian snakes its diagnosis is still extremely problematic. Until recently diagnosis was purely histological, determined by the presence of inclusion bodies. However, inclusion bodies are not specific to IBD and are found in many viral infections. It seems entirely plausible that at least some of the snakes diagnosed with IBD were infected with a different virus. Recently arenavirus has been identified in snakes with IBD. A diagnostic test is now available in Australia. The effect of IBD on wild Australian snake populations is unknown as the IBD status of Australia’s snakes, captive and free living, is also unknown. Aetiology Previously it was thought that IBD may be caused by a virus of the family Retroviridae (Schumacher et al. 1994). Although retroviruses have been isolated from affected snakes it has not been shown definitely that they were the cause of the disease (Jacobson et al. 2001). More recently researchers have found arenaviruses in six out of eight snakes diagnosed with IBD in the USA and eight IBD positive snakes examined in The Netherlands. These findings led the authors to speculate that arenavirus may be the causative agent of IBD (Stenglein et al. 2012; Bodewes et al. 2013). Natural hosts IBD is mainly a disease of the family Boidae (boas and pythons) but cases have also been described in an eastern kingsnake (Lampropeltis getulus), and a collection of palm vipers (Bothriechis marchi) (Raymond et al. -
NSW REPTILE KEEPERS' LICENCE Species Lists 1006
NSW REPTILE KEEPERS’ LICENCE SPECIES LISTS (2006) The taxonomy in this list follows that used in Wilson, S. and Swan, G. A Complete Guide to Reptiles of Australia, Reed 2003. Common names generally follow the same text, when common names were used, or have otherwise been lifted from other publications. As well as reading this species list, you will also need to read the “NSW Reptile Keepers’ Licence Information Sheet 2006.” That document has important information about the different types of reptile keeper licenses. It also lists the criteria you need to demonstrate before applying to upgrade to a higher class of licence. THESE REPTILES CAN ONLY BE HELD UNDER A REPTILE KEEPERS’ LICENCE OF CLASS 1 OR HIGHER Code Scientific Name Common Name Code Scientific Name Common Name Turtles Monitors E2018 Chelodina canni Cann’s Snake-necked Turtle G2263 Varanus acanthurus Spiney-tailed Monitor C2017 Chelodina longicollis Snake-necked Turtle Q2268 Varanus gilleni Pygmy Mulga Monitor G2019 Chelodina oblonga Oblong Turtle G2271 Varanus gouldii Sand Monitor Y2028 Elseya dentata Northern Snapping Turtle M2282 Varanus tristis Black-Headed Monitor K2029 Elseya latisternum Saw-shelled Turtle Y2776 Elusor macrurus Mary River Turtle E2034 Emydura macquarii Murray Short-necked Turtle Skinks T2031 Emydura macquarii dharra Macleay River Turtle A2464 Acritoscincus platynotum Red-throated Skink T2039 Emydura macquarii dharuk Sydney Basin Turtle W2331 Cryptoblepharus virgatus Cream-striped Wall Skink T2002 Emydura macquarii emmotti Emmott’s Short-necked Turtle W2375 -
Genus Antaresia
MONITOR - JOURNAL OF THE VICTORIAN HERPETOLOGICAL SOCIETY 10 (2/3) 1999:24-32MONITOR Copyright - JOURNALVictorian OFHerpetological THE VICTORIAN Society HERPETOLOGICAL SOCIETY 10 (2/3) 1999 AUSTRALIA’S DWARF PYTHONS – GENUS ANTARESIA RAYMOND T. HOSER 41 Village Avenue, Doncaster, Victoria, 3108, Australia. Phone:+61 3 9857-4491 Fax: +61 3 9857-4664 E-mail: [email protected] INTRODUCTION comment as dogma, readers should be aware that it Australia’s dwarf pythons were, until the early 1980’s, has been argued by some that the Wells and Wellington classified by most herpetologists as a single species, description was inadequate in terms of diagnostic namely the Children’s Python (Liasis childreni). An information and is therefore invalid. Wells and 1873 classification of the eastern form ‘maculosus’ had Wellington counter that their information as printed is long been regarded as being a junior synonym and sufficient as per ICZN rules, particularly when thus a part of the same species. Few herpetologists in referenced with the specimen lodged at a public the early 1980’s were even aware that such a synonymy museum, to wit the Australian Museum in Sydney. even existed. However the preceding dispute is probably not the main Things began to change when in 1981 I wrote a paper reason why the Wells and Wellington name wasn’t formally describing the Western Australian form as a adopted by most authors following its publication. You new species. At the same time I also sought to see shortly thereafter there was a petition to the ICZN redescribe the Ant-hill Python as Liasis perthensis (as by a substantial number of Australian herpetologists a full species) in a separate paper, which was by that that called for the complete suppression of three works stage erroneously regarded by most as being an invalid by Wells and Wellington (1984, 1985a, 1985b), which name applied to western populations of the so-called included the one relevant here. -
Review of Species Selected on the Basis of the Analysis of 2016 CITES Export Quotas
UNEP-WCMC technical report Review of species selected on the basis of the Analysis of 2016 CITES export quotas (Version edited for public release) Review of species selected on the basis of the Analysis of 2016 CITES export quotas. Prepared for The European Commission, Directorate General Environment, Directorate E - Global & Regional Challenges, LIFE ENV.E.2. – Global Sustainability, Trade & Multilateral Agreements, Brussels, Belgium Published September 2016 Copyright European Commission 2016 Citation UNEP-WCMC. 2016. Review of species selected on the basis of the Analysis of 2016 CITES export quotas. UNEP-WCMC, Cambridge. The UNEP World Conservation Monitoring Centre (UNEP-WCMC) is the specialist biodiversity assessment centre of the United Nations Environment Programme, the world’s foremost intergovernmental environmental organization. The Centre has been in operation for over 30 years, combining scientific research with policy advice and the development of decision tools. We are able to provide objective, scientifically rigorous products and services to help decision-makers recognize the value of biodiversity and apply this knowledge to all that they do. To do this, we collate and verify data on biodiversity and ecosystem services that we analyze and interpret in comprehensive assessments, making the results available in appropriate forms for national and international level decision-makers and businesses. To ensure that our work is both sustainable and equitable we seek to build the capacity of partners where needed, so that they can provide the same services at national and regional scales. The contents of this report do not necessarily reflect the views or policies of UNEP, contributory organisations or editors. The designations employed and the presentations do not imply the expressions of any opinion whatsoever on the part of UNEP, the European Commission or contributory organisations, editors or publishers concerning the legal status of any country, territory, city area or its authorities, or concerning the delimitation of its frontiers or boundaries. -
Final Environmental Assessment for Listing Large Constrictor Snakes As Injurious Wildlife Under the Lacey Act
Final Environmental Assessment For Listing Large Constrictor Snakes As Injurious Wildlife under the Lacey Act Python molurus [including Burmese python (Python molurus bivittatus) and Indian python (Python molurus molurus)], Northern African Python (Python sebae), Southern African Python (Python natalensis), and Yellow Anaconda (Eunectes notaeus), Prepared by: U.S. Fish and Wildlife Service South Florida Ecological Services Office 1339 20th Street Vero Beach, Florida 32960 January 2012 Abstract This document contains a Final Environmental Assessment (EA), which examines the potential environmental impacts of the Proposed Action to list as injurious nine large constrictor snake species including Python molurus [Burmese python (Python molurus bivittatus) and Indian python (Python molurus molurus); also referred to as Burmese python below unless otherwise noted], reticulated python (Broghammerus reticulatus or Python reticulatus), Northern African python (Python sebae), Southern African python (Python natalensis), boa constrictor (Boa constrictor), yellow anaconda (Eunectes notaeus), DeSchauensee’s anaconda (Eunectes deschauenseei), green anaconda (Eunectes murinus), and Beni anaconda (Eunectes beniensis)]. The draft environmental assessment was released to the public for review and comment on March 12, 2010. All public comments received regarding the draft environmental assessment are presented in the Appendix of this document, along with the U.S. Fish and Wildlife Service’s written response to each comment. In this environmental assessment, -
Hdl 111334.Pdf
SUBMITTED VERSION This is the pre-peer reviewed version of the following article: Damien Esquerré, Emma Sherratt, J. Scott Keogh Evolution of extreme ontogenetic allometric diversity and heterochrony in pythons, a clade of giant and dwarf snakes Evolution, 2017; 71(12):2829-2844 © 2017 The Author(s). Evolution © 2017 The Society for the Study of Evolution. which has been published in final form at http://dx.doi.org/10.1111/evo.13382. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions." PERMISSIONS https://authorservices.wiley.com/author-resources/Journal-Authors/licensing/self-archiving.html Submitted (preprint) Version The submitted version of an article is the author's version that has not been peer-reviewed, nor had any value added to it by Wiley (such as formatting or copy editing). The submitted version may be placed on: the author's personal website the author's company/institutional repository or archive not for profit subject-based preprint servers or repositories Self-archiving of the submitted version is not subject to an embargo period. We recommend including an acknowledgement of acceptance for publication and, following the final publication, authors may wish to include the following notice on the first page: "This is the pre-peer reviewed version of the following article: [FULL CITE], which has been published in final form at [Link to final article using the DOI]. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self- Archived Versions." The version posted may not be updated or replaced with the accepted version (except as provided below) or the final published version (the Version of Record).