Bearded Dragon by Catherine Love, DVM Updated 2021
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Temperature-Induced Colour Change Varies Seasonally in Bearded
applyparastyle "body/p[1]" parastyle "Text_First" Biological Journal of the Linnean Society, 2018, 123, 422–430. With 4 figures. Temperature-induced colour change varies seasonally in Downloaded from https://academic.oup.com/biolinnean/article-abstract/123/2/422/4774525 by University of Melbourne Library user on 01 November 2018 bearded dragon lizards VIVIANA CADENA,1* KATRINA RANKIN,1 KATHLEEN R. SMITH,1 JOHN A. ENDLER,2 and DEVI STUART-FOX1 1School of BioSciences, The University of Melbourne, Parkville, VIC 3010, Australia 2Centre for Integrative Ecology, School of Life and Environmental Sciences, Deakin University, Waurn Ponds, VIC 3220, Australia Received 14 September 2017; revised 17 November 2017; accepted for publication 18 November 2017 The benefits of colour change are expected to vary seasonally because of changes in reproductive activity, tem- perature and, potentially, predation risk; yet temporal variation in colour change has seldom been examined. We measured colour change in spring and autumn using captive individuals from two differently coloured populations of the central bearded dragon lizard, Pogona vitticeps. We predicted that colour change should be greater in spring than autumn because of the added requirements of reproductive and territorial activity. To elicit colour change in a standardized way, we placed lizards inside temperature-controlled chambers and measured colour at 15, 25, 35 and 40 °C, repeating experiments in spring and autumn. Lizards from both populations changed from dark grey to light yellowish or orange-brown (increasing luminance and saturation) with increasing temperature in both seasons, and both populations changed colour to a similar extent. As predicted, the maximal extent of temperature-induced colour change (in particular, luminance change) was greater in spring than autumn. -
Intelligence of Bearded Dragons Sydney Herndon
Murray State's Digital Commons Honors College Theses Honors College Spring 4-26-2021 Intelligence of Bearded Dragons sydney herndon Follow this and additional works at: https://digitalcommons.murraystate.edu/honorstheses Part of the Behavior and Behavior Mechanisms Commons Recommended Citation herndon, sydney, "Intelligence of Bearded Dragons" (2021). Honors College Theses. 67. https://digitalcommons.murraystate.edu/honorstheses/67 This Thesis is brought to you for free and open access by the Honors College at Murray State's Digital Commons. It has been accepted for inclusion in Honors College Theses by an authorized administrator of Murray State's Digital Commons. For more information, please contact [email protected]. Intelligence of Bearded Dragons Submitted in partial fulfillment of the requirements for the Murray State University Honors Diploma Sydney Herndon 04/2021 i Abstract The purpose of this thesis is to study and explain the intelligence of bearded dragons. Bearded dragons (Pogona spp.) are a species of reptile that have been popular in recent years as pets. Until recently, not much was known about their intelligence levels due to lack of appropriate research and studies on the species. Scientists have been studying the physical and social characteristics of bearded dragons to determine if they possess a higher intelligence than previously thought. One adaptation that makes bearded dragons unique is how they respond to heat. Bearded dragons optimize their metabolic functions through a narrow range of body temperatures that are maintained through thermoregulation. Many of their behaviors are temperature dependent, such as their speed when moving and their food response. When they are cold, these behaviors decrease due to their lower body temperature. -
Niche Modeling for the Genus Pogona (Squamata: Agamidae) in Australia: Predicting Past (Late Quaternary) and Future (2070) Areas of Suitable Habitat
Niche modeling for the genus Pogona (Squamata: Agamidae) in Australia: predicting past (late Quaternary) and future (2070) areas of suitable habitat Julie E. Rej1,2 and T. Andrew Joyner2 1 Department of Wildlife Ecology, The Wilds, Cumberland, OH, USA 2 Department of Geosciences, East Tennessee State University, Johnson City, TN, USA ABSTRACT Background: As the climate warms, many species of reptiles are at risk of habitat loss and ultimately extinction. Locations of suitable habitat in the past, present, and future were modeled for several lizard species using MaxEnt, incorporating climatic variables related to temperature and precipitation. In this study, we predict where there is currently suitable habitat for the genus Pogona and potential shifts in habitat suitability in the past and future. Methods: Georeferenced occurrence records were obtained from the Global Biodiversity Information Facility, climate variables (describing temperature and precipitation) were obtained from WorldClim, and a vegetation index was obtained from AVHRR satellite data. Matching climate variables were downloaded for three different past time periods (mid-Holocene, Last Glacial Maximum, and Last Interglacial) and two different future projections representative concentration pathways (RCPs 2.6 and 8.5). MaxEnt produced accuracy metrics, response curves, and probability surfaces. For each species, parameters were adjusted for the best possible output that was biologically informative. Results: Model results predicted that in the past, there was little suitable habitat for P. henrylawsoni and P. microlepidota within the areas of their current range. Past areas of suitable habitat for P. barbata were predicted to be similar to the current 16 March 2018 Submitted prediction. Pogona minor and P. -
Bearded Dragon (Pogona Vitticeps) Care Compiled by Dr
Bearded Dragon (Pogona vitticeps) Care Compiled by Dr. Dayna Willems Brief Description Native to the arid regions of Australia, bearded dragons are popular pets in captivity due to their docile nature and fairly basic care requirements compared to other reptiles. Adults can get up to two feet in length. There are several color morphs available like citrus, tangerine, and reds, and then several based on their scale texture as well. Lifespan With good care the average lifespan is about 8-10 years. Sexing Determining the gender of your bearded dragon can be difficult, especially as juveniles. Beard color is not a reliable indicator. Males will head bob to attract a female but some females will also head bob as a show of dominance. If you look at the underside of the tail just past the vent males should have two bulges side by side where the hemipenes (reproductive organs) sit in the base of the tail. Females will not have this. If your beardie's hemipenes briefly come out of the body while defecating then it is definitely male. Males also tend to have larger femoral pores as adults that can fill with waxy substance (normal). Caging • Juveniles: At least 20 gallon tank. • Adults: At least 40 gallon tank. • One bearded dragon per cage. Substrate • Newspaper, artificial turf like reptile carpet, flat stones or no floor covering are best. • AVOID sand (especially calcium sand) and bark/mulch should - your dragon might consume sand or fine- particle products on the cage floor, and this could lead to intestinal impaction. • A flat rock under the basking light will warm evenly and provide a good basking spot. -
Adenoviruses in Free-Ranging Australian Bearded Dragons
Veterinary Microbiology 234 (2019) 72–76 Contents lists available at ScienceDirect Veterinary Microbiology journal homepage: www.elsevier.com/locate/vetmic Adenoviruses in free-ranging Australian bearded dragons (Pogona spp.) T ⁎ Timothy H Hyndmana, Jonathon G Howardb, Robert JT Doneleyc, a Murdoch University, School of Veterinary Medicine, Murdoch, Western Australia, 6150, Australia b Exovet Pty Ltd., East Maitland, New South Wales, 2323, Australia c UQ Veterinary Medical Centre, University of Queensland, School of Veterinary Science, Gatton, Queensland 4343, Australia ARTICLE INFO ABSTRACT Keywords: Adenoviruses are a relatively common infection of reptiles globally and are most often reported in captive Helodermatid adenovirus 2 central bearded dragons (Pogona vitticeps). We report the first evidence of adenoviruses in bearded dragons in Atadenovirus their native habitat in Australia. Oral-cloacal swabs and blood samples were collected from 48 free-ranging Diagnostics bearded dragons from four study populations: western bearded dragons (P. minor minor) from Western Australia Diagnosis (n = 4), central bearded dragons (P. vitticeps) from central Australia (n = 2) and western New South Wales (NSW) (n = 29), and coastal bearded dragons (P. barbata) from south-east Queensland (n = 13). Samples were tested for the presence of adenoviruses using a broadly reactive (pan-adenovirus) PCR and a PCR specific for agamid adenovirus-1. Agamid adenovirus-1 was detected in swabs from eight of the dragons from western NSW and one of the coastal bearded dragons. Lizard atadenovirus A was detected in one of the dragons from western NSW. Adenoviruses were not detected in any blood sample. All bearded dragons, except one, were apparently healthy and so finding these adenoviruses in these animals is consistent with bearded dragons being natural hosts for these viruses. -
Bearded Dragons Native to Australia
BEARDED DRAGON CARE There are many species of Bearded Dragons native to Australia. The main species kept in captivity include the Eastern Beared Dragon Pogona barbata, Central Bearded Dragon Pogona vitticeps and Pygmy Bearded Dragon Pogona henrylawsoni. Their gentle nature & somewhat curious behaviours can make them interesting pets. Some Dragons will grow to around 50-60cm in length (including tail) & live to around 12-15 years. Below is an outline of the ‘basic’ requirements for keeping Dragons as pets. Please note: All Australian Dragon lizards are protected species in Australia. Seek individual state & territory requirements for legalities on keeping Dragons as pets. Housing .Bearded Dragons can be housed indoors. They require suitable artificial heat & light sources as outlined below .Suitable enclosures include plastic tubs or plastic-fronted cabinets at least 1m long x 0.5m wide .Enclosure set-up depends on the size/age of the Dragon. Provide ‘hide’ boxes & branches to climb & ‘bask’ on .Substrates (enclosure floor covering) are most simply & hygienically provided by means of newspaper or recycled paper kitty litter. Artificial grass can also make a good, easy to clean substrate option .Disinfect cages each week (use bleach diluted 1:10 with water. Rinse well afterwards). ‘Spot’ clean as necessary .Dragons are territorial. Adult males will often fight if housed together .A shallow water bowl can be offered. Ensure the Dragon can’t drown in it. For juveniles it is necessary to spray them daily with water for them to drink. Avoid large water bowls, Dragons come from dry areas & prefer lower humidity .Heating. Provide them with a ‘temperature gradient’ in their enclosure. -
Code of Practice Captive Reptile and Amphibian Husbandry Nature Conservation Act 1992
Code of Practice Captive Reptile and Amphibian Husbandry Nature Conservation Act 1992 ♥ The State of Queensland, Department of Environment and Science, 2020 Copyright protects this publication. Except for purposes permitted by the Copyright Act, reproduction by whatever means is prohibited without prior written permission of the Department of Environment and Science. Requests for permission should be addressed to Department of Environment and Science, GPO Box 2454 Brisbane QLD 4001. Author: Department of Environment and Science Email: [email protected] Approved in accordance with section 174A of the Nature Conservation Act 1992. Acknowledgments: The Department of Environment and Science (DES) has prepared this code in consultation with the Department of Agriculture, Fisheries and Forestry and recreational reptile and amphibian user groups in Queensland. Human Rights compatibility The Department of Environment and Science is committed to respecting, protecting and promoting human rights. Under the Human Rights Act 2019, the department has an obligation to act and make decisions in a way that is compatible with human rights and, when making a decision, to give proper consideration to human rights. When acting or making a decision under this code of practice, officers must comply with that obligation (refer to Comply with Human Rights Act). References referred to in this code- Bustard, H.R. (1970) Australian lizards. Collins, Sydney. Cann, J. (1978) Turtles of Australia. Angus and Robertson, Australia. Cogger, H.G. (2018) Reptiles and amphibians of Australia. Revised 7th Edition, CSIRO Publishing. Plough, F. (1991) Recommendations for the care of amphibians and reptiles in academic institutions. National Academy Press: Vol.33, No.4. -
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 -
Developmental Asynchrony and Antagonism of Sex Determination
www.nature.com/scientificreports OPEN Developmental asynchrony and antagonism of sex determination pathways in a lizard with Received: 18 July 2018 Accepted: 19 September 2018 temperature-induced sex reversal Published: xx xx xxxx Sarah L. Whiteley 1,2,3, Vera Weisbecker 3, Arthur Georges 1, Arnault Roger Gaston Gauthier 4, Darryl L. Whitehead4 & Clare E. Holleley 1,2 Vertebrate sex diferentiation follows a conserved suite of developmental events: the bipotential gonads diferentiate and shortly thereafter sex specifc traits become dimorphic. However, this may not apply to squamates, a diverse vertebrate lineage comprising of many species with thermosensitive sexual development. Of the three species with data on the relative timing of gonad diferentiation and genital dimorphism, the females of two (Niveoscincus ocellatus and Barisia imbricata) exhibit a phase of temporary pseudohermaphroditism or TPH (gonads have diferentiated well before genital dimorphism). We report a third example of TPH in Pogona vitticeps, an agamid with temperature- induced male to female sex reversal. These fndings suggest that for female squamates, genital and gonad development may not be closely synchronised, so that TPH may be common. We further observed a high frequency of ovotestes, a usually rare gonadal phenotype characterised by a mix of male and female structures, exclusively associated with temperature-induced sex reversal. We propose that ovotestes are evidence of a period of antagonism between male and female sex-determining pathways during sex reversal. Female sexual development in squamates is considerably more complex than has been appreciated, providing numerous avenues for future exploration of the genetic and hormonal cues that govern sexual development. -
Pathogenesis of Isospora Amphiboluri in Bearded Dragons (Pogona Vitticeps)
animals Article Pathogenesis of Isospora amphiboluri in Bearded Dragons (Pogona vitticeps) Michael Walden and Mark A. Mitchell * School of Veterinary Medicine, Louisiana State University, Skip Bertman Drive, Baton Rouge, LA 70803, USA; [email protected] * Correspondence: [email protected]; Tel.: +1-225-921-6803 Simple Summary: Coccidia are common parasites of captive animals. While there have been a number of studies evaluating the life cycles of these parasites in domestic pets and livestock, there has been limited research assessing the impact of these parasites on reptiles. Bearded dragons are a common pet lizard and are known to be infected by their own species of coccidia, Isospora amphiboluri. To determine the best practices for controlling this parasite in captive bearded dragons, it is important that we learn about what the parasite does once it infects the bearded dragon. This study found that Isospora amphiboluri infects the small and large intestines of bearded dragons. In addition, the time (pre-patent period) from exposure to shedding the parasite in feces is 15–22 days. This information is important for developing treatment and management protocols for captive bearded dragons to reduce their exposure to this parasite. Abstract: Isospora amphiboluri is a common coccidian found in captive bearded dragons (Pogona vitticeps). To minimize the impact of this parasite, it is important to characterize its pathogenesis so that we can develop appropriate methods for diagnosis and treatment. Forty-five juvenile bearded dragons were used for this two-part study. In the first part, ten bearded dragons were infected with 20,000 oocysts per os, while a control group of five animals received only water. -
2011: Husbandry, Diseases and Veterinary Care of The
MASTER CLASS HUSBANDRY, DISEASES AND VETERINARY CARE OF THE BEARDED DRAGON, Pogona vitticeps Paul Raiti, DVM, DABVP (Reptile and Amphibian Practice) Beverlie Animal Hospital, Mt. Vernon, NY 10552, USA ABSTRACT: Bearded dragons are a popular reptile. This paper reviews natural history, husbandry, behavior, nutrition, and reproduction of the bearded dragon. In addition, important aspects of physical examination, diagnostic techniques, and common diseases are included. KEY WORDS: bearded dragon INTRODUCTION The bearded dragon’s (Pogona vitticeps) appearance, docility, captive hardiness, omnivorous diet, diurnal activity and manageable size (<20 in) have combined to make this reptile very popular (Christie, 1993). Several pairs were imported from Germany in the 1980’s and were the founding stock of the captive population in the United States today. Bearded dragons consist of 8 species all of which are from the eastern and central (inland) parts of Australia (Weis, 2001). The “true” Rankin’s dragon (P. henrylawsoni ) is rarely available in the pet industry due to health issues associated with inbreeding and hybridization with P. vitticeps. The inland species has proven to be the most hardy and consistently reproductive in captivity. Assorted color varieties and sizes are available in the pet trade including sandfire and pastel color morphs and the so called “German giants.” Most recently, there are dragons with reduced scale size (leatherbacks) and scaleless (silkbacks) mutations. Lack of genetic diversity may be a contributing factor for unthriftiness and susceptibility to disease. NATURAL HISTORY Bearded dragons belong to the family Agamidae. Agamids are the fourth largest family of lizards with some 300 species spread throughout Africa across Asia and into Australia. -
Chlamydosaurus Kingii) and Bearded Dragon (Pogona Vitticeps
LUCRĂRI ŞTIINłIFICE MEDICINĂ VETERINARĂ VOL. XLII (1), 2009, TIMIŞOARA ADVOCATE – THERAPEUTICAL SOLUTION IN PARASITICAL INFESTATION IN FRILLNECK LIZARD ( CHLAMYDOSAURUS KINGII ) AND BEARDED DRAGON ( POGONA VITTICEPS ) AMA GROZA¹, NARCISA MEDERLE², GH. DĂRĂBU޲ ¹Veterinary praxis Super Pet ²Faculty of Veterinary Medicine Timisoara, Department of Parasitology, 119 Calea Aradului, 300645,Timiaoara, Romania Summary This is the first study in treatment with Advocate in bearded dragon ( Pogona vitticeps ) and for frillneck lizard ( Chlamydosaurus kingii ) that has been made in Roumania. Six bearded dragon ( Pogona vitticeps ) and for frillneck lizard ( Chlamydosaurus kingii ) were examined by clinical method. The faeces samples were examined by direct smear method and Willis method. The pacients were treated with Advocate (imidacloprid and moxidectin), spot-on administration, 0,2 ml/kg, repeated after 14 days (total 3 treatments). The treatment was efficacious and faecal samples were Kalicephalus and Oxiuris negative. Treatment with Advocate did not eliminate Isospora oocysts . Key words : advocate, frillineck lizard, bearded dragon, parasitical infestation In 1972, Ippen revealed that in necropsies performed on over 1100 reptiles from a zoological parc 40% of the specimens were actively infested with parasites; in 79% in this cases parasites were incrimined as the cause of deadh. In 1983, the parasitic lesions were found second to bacterial lesions among necropsy findings in captive reptiles. These dates emphasis the importance of parasites to the rapidly emerging fields of herpetoculture and reptile veterinary medicine. Faecal samples are examined for the presence of protozoans, parasitic ova and larvae. Excretions from the reptile cloaca are often a mixture of urine, urates and faeces. Parasites can be diagnose from faecal smears and flotations, as well as from other samples and by visual inspection (2, 5, 7).