Bonner Zoologische Beiträge
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<I>Morethia</I> (Lacertilia: Scincidae)
A NEW SPECIES OF MORETHIA (LACERTILlA: SCINCIDAE) FROM NORTHERN AUSTRALIA, WITH COMMENTS ON THE BIOLOGY AND RELATIONSHIPS OF THE GENUS ALLEN E. GREER The Australian Museum, Sydney ABSTRACT Morethia is a genus of Iygosomine skinks endemic to Australia. This paper provides a description of a new species of Morethia from northern Australia, a diagonsis of the genus, and a discussion of its intra and intergeneric relationships. It also includes a key to the eight currently recognized species of Morethia and notes on their colour pattern, reproduction, behaviour, habitat and distribution. A NEW SPECIES OF MORETHIA In his revision of the Western Australian species of the endemic Australian genus Morethia, Storr (1972) noted that the form ruficauda was "replaced by an undescribed race" in the far north of the Northern Territory. A few years later while reviewing the genus, I "rediscovered" this undescribed form and interpreted it as a distinct species. Dr Storr has graciously allowed me to describe this species, and in appreciation of his original contribution to the taxonomy of the genus (Storr 1972), I take pleasure in naming it Marethia starri New Species Figs 1, 2 (top), and 9 HOLOTYPE: Northern Territory Museum R 1815 - 4.5 km. S. of Noonamah, Northern Territory (12°40' 5., 131°04' E.). Collected by Messrs G. F. Gow and R. W. Wells on 10 November 1975. PARATYPES: Unless speCifically mentioned otherwise, all localities are in the extreme northern part of the Northern Territory. Australian Museum: R 12384 - Yirrkala; R 17411 - Port Keats Mission; R 37225- Koongarra, Mt. Brockman Range; R 41960 - Maningrida Settlement; R 71991- Yirrkala; R 72862 - appox. -
Resource Allocation to Reproduction in Animals
Biol. Rev. (2014), 89, pp. 849–859. 849 doi: 10.1111/brv.12082 Resource allocation to reproduction in animals Sebastiaan A. L. M. Kooijman1,∗ and Konstadia Lika2 1Department of Theoretical Biology, VU University Amsterdam, de Boelelaan 1087, 1081 HV Amsterdam, The Netherlands 2Department of Biology, University of Crete, Voutes University Campus, 70013 Heraklion, Crete, Greece ABSTRACT The standard Dynamic Energy Budget (DEB) model assumes that a fraction κ of mobilised reserve is allocated to somatic maintenance plus growth, while the rest is allocated to maturity maintenance plus maturation (in embryos and juveniles) or reproduction (in adults). All DEB parameters have been estimated for 276 animal species from most large phyla and all chordate classes. The goodness of fit is generally excellent. We compared the estimated values of κ with those that would maximise reproduction in fully grown adults with abundant food. Only 13% of these species show a reproduction rate close to the maximum possible (assuming that κ can be controlled), another 4% have κ lower than the optimal value, and 83% have κ higher than the optimal value. Strong empirical support hence exists for the conclusion that reproduction is generally not maximised. We also compared the parameters of the wild chicken with those of races selected for meat and egg production and found that the latter indeed maximise reproduction in terms of κ, while surface-specific assimilation was not affected by selection. We suggest that small values of κ relate to the down-regulation of maximum body size, and large values to the down-regulation of reproduction. We briefly discuss the ecological context for these findings. -
The Herpetofauna of Timor-Leste: a First Report 19 Doi: 10.3897/Zookeys.109.1439 Research Article Launched to Accelerate Biodiversity Research
A peer-reviewed open-access journal ZooKeys 109: 19–86 (2011) The herpetofauna of Timor-Leste: a first report 19 doi: 10.3897/zookeys.109.1439 RESEARCH ARTICLE www.zookeys.org Launched to accelerate biodiversity research The herpetofauna of Timor-Leste: a first report Hinrich Kaiser1, Venancio Lopes Carvalho2, Jester Ceballos1, Paul Freed3, Scott Heacox1, Barbara Lester3, Stephen J. Richards4, Colin R. Trainor5, Caitlin Sanchez1, Mark O’Shea6 1 Department of Biology, Victor Valley College, 18422 Bear Valley Road, Victorville, California 92395, USA; and The Foundation for Post-Conflict Development, 245 Park Avenue, 24th Floor, New York, New York 10167, USA 2 Universidade National Timor-Lorosa’e, Faculdade de Ciencias da Educaçao, Departamentu da Biologia, Avenida Cidade de Lisboa, Liceu Dr. Francisco Machado, Dili, Timor-Leste 3 14149 S. Butte Creek Road, Scotts Mills, Oregon 97375, USA 4 Conservation International, PO Box 1024, Atherton, Queensland 4883, Australia; and Herpetology Department, South Australian Museum, North Terrace, Adelaide, South Australia 5000, Australia 5 School of Environmental and Life Sciences, Charles Darwin University, Darwin, Northern Territory 0909, Australia 6 West Midland Safari Park, Bewdley, Worcestershire DY12 1LF, United Kingdom; and Australian Venom Research Unit, Department of Pharmacology, University of Melbourne, Vic- toria 3010, Australia Corresponding author: Hinrich Kaiser ([email protected]) Academic editor: Franco Andreone | Received 4 November 2010 | Accepted 8 April 2011 | Published 20 June 2011 Citation: Kaiser H, Carvalho VL, Ceballos J, Freed P, Heacox S, Lester B, Richards SJ, Trainor CR, Sanchez C, O’Shea M (2011) The herpetofauna of Timor-Leste: a first report. ZooKeys 109: 19–86. -
An Annotated Type Catalogue of the Dragon Lizards (Reptilia: Squamata: Agamidae) in the Collection of the Western Australian Museum Ryan J
RECORDS OF THE WESTERN AUSTRALIAN MUSEUM 34 115–132 (2019) DOI: 10.18195/issn.0312-3162.34(2).2019.115-132 An annotated type catalogue of the dragon lizards (Reptilia: Squamata: Agamidae) in the collection of the Western Australian Museum Ryan J. Ellis Department of Terrestrial Zoology, Western Australian Museum, Locked Bag 49, Welshpool DC, Western Australia 6986, Australia. Biologic Environmental Survey, 24–26 Wickham St, East Perth, Western Australia 6004, Australia. Email: [email protected] ABSTRACT – The Western Australian Museum holds a vast collection of specimens representing a large portion of the 106 currently recognised taxa of dragon lizards (family Agamidae) known to occur across Australia. While the museum’s collection is dominated by Western Australian species, it also contains a selection of specimens from localities in other Australian states and a small selection from outside of Australia. Currently the museum’s collection contains 18,914 agamid specimens representing 89 of the 106 currently recognised taxa from across Australia and 27 from outside of Australia. This includes 824 type specimens representing 45 currently recognised taxa and three synonymised taxa, comprising 43 holotypes, three syntypes and 779 paratypes. Of the paratypes, a total of 43 specimens have been gifted to other collections, disposed or could not be located and are considered lost. An annotated catalogue is provided for all agamid type material currently and previously maintained in the herpetological collection of the Western Australian Museum. KEYWORDS: type specimens, holotype, syntype, paratype, dragon lizard, nomenclature. INTRODUCTION Australia was named by John Edward Gray in 1825, The Agamidae, commonly referred to as dragon Clamydosaurus kingii Gray, 1825 [now Chlamydosaurus lizards, comprises over 480 taxa worldwide, occurring kingii (Gray, 1825)]. -
Mitochondrial Genomes of Two Polydora
www.nature.com/scientificreports OPEN Mitochondrial genomes of two Polydora (Spionidae) species provide further evidence that mitochondrial architecture in the Sedentaria (Annelida) is not conserved Lingtong Ye1*, Tuo Yao1, Jie Lu1, Jingzhe Jiang1 & Changming Bai2 Contrary to the early evidence, which indicated that the mitochondrial architecture in one of the two major annelida clades, Sedentaria, is relatively conserved, a handful of relatively recent studies found evidence that some species exhibit elevated rates of mitochondrial architecture evolution. We sequenced complete mitogenomes belonging to two congeneric shell-boring Spionidae species that cause considerable economic losses in the commercial marine mollusk aquaculture: Polydora brevipalpa and Polydora websteri. The two mitogenomes exhibited very similar architecture. In comparison to other sedentarians, they exhibited some standard features, including all genes encoded on the same strand, uncommon but not unique duplicated trnM gene, as well as a number of unique features. Their comparatively large size (17,673 bp) can be attributed to four non-coding regions larger than 500 bp. We identifed an unusually large (putative) overlap of 14 bases between nad2 and cox1 genes in both species. Importantly, the two species exhibited completely rearranged gene orders in comparison to all other available mitogenomes. Along with Serpulidae and Sabellidae, Polydora is the third identifed sedentarian lineage that exhibits disproportionally elevated rates of mitogenomic architecture rearrangements. Selection analyses indicate that these three lineages also exhibited relaxed purifying selection pressures. Abbreviations NCR Non-coding region PCG Protein-coding gene Metazoan mitochondrial genomes (mitogenomes) usually encode the set of 37 genes, comprising 2 rRNAs, 22 tRNAs, and 13 proteins, encoded on both genomic strands. -
Fowlers Gap Biodiversity Checklist Reptiles
Fowlers Gap Biodiversity Checklist ow if there are so many lizards then they should make tasty N meals for someone. Many of the lizard-eaters come from their Reptiles own kind, especially the snake-like legless lizards and the snakes themselves. The former are completely harmless to people but the latter should be left alone and assumed to be venomous. Even so it odern reptiles are at the most diverse in the tropics and the is quite safe to watch a snake from a distance but some like the Md rylands of the world. The Australian arid zone has some of the Mulga Snake can be curious and this could get a little most diverse reptile communities found anywhere. In and around a disconcerting! single tussock of spinifex in the western deserts you could find 18 species of lizards. Fowlers Gap does not have any spinifex but even he most common lizards that you will encounter are the large so you do not have to go far to see reptiles in the warmer weather. Tand ubiquitous Shingleback and Central Bearded Dragon. The diversity here is as astonishing as anywhere. Imagine finding six They both have a tendency to use roads for passage, warming up or species of geckos ranging from 50-85 mm long, all within the same for display. So please slow your vehicle down and then take evasive genus. Or think about a similar diversity of striped skinks from 45-75 action to spare them from becoming a road casualty. The mm long! How do all these lizards make a living in such a dry and Shingleback is often seen alone but actually is monogamous and seemingly unproductive landscape? pairs for life. -
Level 2 Fauna Survey.Pdf
Fauna Survey (Level 2) Phase 1 (September 2016) and Phase 2 (April 2017) Lake Wells Potash Project Australian Potash Ltd September 2017 Report Number: 01-000017-1/2 VERSION 4 On behalf of: Australian Potash Limited PO Box 1941 WEST PERTH, WA 6872 Prepared by: Greg Harewood Zoologist PO Box 755 BUNBURY WA 6231 M: 0402 141 197 E: [email protected] LAKE WELLS POTASH PROJECT – AUSTRALIAN POTASH LTD – L2 FAUNA SURVEY - PHASE 1 & 2 – SEPTEMBER 2017 – V4 TABLE OF CONTENTS SUMMARY .............................................................................................................. III 1. INTRODUCTION ............................................................................................... 1 1.1 BACKGROUND ................................................................................................ 1 1.2 SURVEY AREA ................................................................................................. 1 1.3 SURVEY SCOPE .............................................................................................. 1 2. METHODS ........................................................................................................ 3 2.1 FAUNA INVENTORY - LITERATURE REVIEW ............................................... 3 2.1.1 Database Searches .................................................................................................................. 3 2.1.2 Previous Fauna Surveys in the Area ........................................................................................ 3 2.2 FAUNA INVENTORY – DETAILED -
Spencer Box 1 a Horn
Pitt Rivers Museum ms collections Spencer papers Box 1 A Horn correspondence Horn Letter 1 [The Adelaide Club] 17 Ap/ 94 Dear Mr. Spencer I am gradually getting things focussed here and think we can get a start on the 3d May [1] re photography I am having a small dark tent made one that can be suspended from the branch of a tree like a huge extinguisher about 4 ft in diameter I am going to take a 1/2 plate Camera with rapid rectilinear lens, and glass plates. You need not bring any rapid plates for your whole plate Camera as in the bright light up there one can get splendid instantaneous results with the Ordinary plate. Please make your Collecting plant as light as is consistent with efficiency as everything has to be carried on camels. Have you ever tried the “Tondeur” developer it is splendid for travelling as it is a one mixture solution and I find gives good results when used even a dozen times, it is a mixture of Hydrogen “Ersine” & can be had at Baker & Rouse’s I told Stirling [2] to write you to engage Keartland [3] Believe me Sincerely yrs WA Horn [4] Horn Letter 2 [The Adelaide Club] 9 June / 94 My dear Spencer, The photos of Ayers Chambers Pillar turned out fairly but a little light fogged & over exposed I got a very good one of a Tempe Downs blackfellow in the act of throwing a spear and another throwing a boomerang. if Gillen [5] has any really good [sic] you might try and get the negatives – When you are turning through the Gibber country get Harry [6] to shew you the hoards made by the ants they really seem to have moved stones by a pound in weight in order to get a clear track— I had a very rough trip by the mail it is really something to remember especially over the Gibbers and the dust was awful I hope you will be able to get Ayers rock as it would be a great addition to the book Sincerely thine [?] W A Horn Horn Letter 3 New University Club St James St. -
Literature Cited in Lizards Natural History Database
Literature Cited in Lizards Natural History database Abdala, C. S., A. S. Quinteros, and R. E. Espinoza. 2008. Two new species of Liolaemus (Iguania: Liolaemidae) from the puna of northwestern Argentina. Herpetologica 64:458-471. Abdala, C. S., D. Baldo, R. A. Juárez, and R. E. Espinoza. 2016. The first parthenogenetic pleurodont Iguanian: a new all-female Liolaemus (Squamata: Liolaemidae) from western Argentina. Copeia 104:487-497. Abdala, C. S., J. C. Acosta, M. R. Cabrera, H. J. Villaviciencio, and J. Marinero. 2009. A new Andean Liolaemus of the L. montanus series (Squamata: Iguania: Liolaemidae) from western Argentina. South American Journal of Herpetology 4:91-102. Abdala, C. S., J. L. Acosta, J. C. Acosta, B. B. Alvarez, F. Arias, L. J. Avila, . S. M. Zalba. 2012. Categorización del estado de conservación de las lagartijas y anfisbenas de la República Argentina. Cuadernos de Herpetologia 26 (Suppl. 1):215-248. Abell, A. J. 1999. Male-female spacing patterns in the lizard, Sceloporus virgatus. Amphibia-Reptilia 20:185-194. Abts, M. L. 1987. Environment and variation in life history traits of the Chuckwalla, Sauromalus obesus. Ecological Monographs 57:215-232. Achaval, F., and A. Olmos. 2003. Anfibios y reptiles del Uruguay. Montevideo, Uruguay: Facultad de Ciencias. Achaval, F., and A. Olmos. 2007. Anfibio y reptiles del Uruguay, 3rd edn. Montevideo, Uruguay: Serie Fauna 1. Ackermann, T. 2006. Schreibers Glatkopfleguan Leiocephalus schreibersii. Munich, Germany: Natur und Tier. Ackley, J. W., P. J. Muelleman, R. E. Carter, R. W. Henderson, and R. Powell. 2009. A rapid assessment of herpetofaunal diversity in variously altered habitats on Dominica. -
Journal of J. G. Macdonald on an Expedition from Port Denison to The
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Frogs & Reptiles NE Vic 2018 Online
Reptiles and Frogs of North East Victoria An Identication and Conservation Guide Victorian Conservation Status (DELWP Advisory List) cr critically endangered en endangered Reptiles & Frogs vu vulnerable nt near threatened dd data deficient L Listed under the Flora and Fauna Guarantee Act (FFG, 1988) Size: of North East Victoria Lizards, Dragons & Skinks: Snout-vent length (cm) Snakes, Goannas: Total length (cm) An Identification and Conservation Guide Lowland Copperhead Highland Copperhead Carpet Python Gray's Blind Snake Nobbi Dragon Bearded Dragon Ragged Snake-eyed Skink Large Striped Skink Frogs: Snout-vent length male - M (mm) Snout-vent length female - F (mm) Austrelaps superbus 170 (NC) Austrelaps ramsayi 115 (PR) Morelia spilota metcalfei – en L 240 (DM) Ramphotyphlops nigrescens 38 (PR) Diporiphora nobbi 8.4 (PR) Pogona barbata – vu 25 (DM) Cryptoblepharus pannosus Snout-Vent 3.5 (DM) Ctenotus robustus Snout-Vent 12 (DM) Guide to symbols Venomous Lifeform F Fossorial (burrows underground) T Terrestrial Reptiles & Frogs SA Semi Arboreal R Rock-dwelling Habitat Type Alpine Bog Montane Forests Alpine Grassland/Woodland Lowland Grassland/Woodland White-lipped Snake Tiger Snake Woodland Blind Snake Olive Legless Lizard Mountain Dragon Marbled Gecko Copper-tailed Skink Alpine She-oak Skink Drysdalia coronoides 40 (PR) Notechis scutatus 200 (NC) Ramphotyphlops proximus – nt 50 (DM) Delma inornata 13 (DM) Rankinia diemensis Snout-Vent 7.5 (NC) Christinus marmoratus Snout-Vent 7 (PR) Ctenotus taeniolatus Snout-Vent 8 (DM) Cyclodomorphus praealtus -
A Brief Overview of the Taxonomy and Nomenclature of the Genus
Australasian Journal of Herpetology 57 Australasian Journal of Herpetology 34:57-63. ISSN 1836-5698 (Print) Published 20 July 2017. ISSN 1836-5779 (Online) A brief overview of the taxonomy and nomenclature of the genus Diplodactylus Gray 1832 sensu lato, with the formal naming of a new subgenus for the Diplodactylus byrnei Lucas and Frost, 1896 species group and two new species within this subgenus. RAYMOND T. HOSER 488 Park Road, Park Orchards, Victoria, 3134, Australia. Phone: +61 3 9812 3322 Fax: 9812 3355 E-mail: snakeman (at) snakeman.com.au Received 25 March 2017, Accepted 28 May 2017, Published 20 July 2017. ABSTRACT The taxonomy of the genus Diplodactylus Gray 1832 sensu lato was well resolved at the genus level by Oliver et al. (2007) and to a lesser extent other authors over the past 30 years to 2017. However a group known as the Wüster gang as detailed by Hoser (2015a-f) have unlawfully stopped most herpetologists from using taxonomy and nomenclature proposed by authors outside of their mob. As a result names formally proposed by Wells and Wellington (1989) for obvious species groups have been forcibly suppressed in herpetology since they were first published. This has remained the case even after Oliver et al. (2007) confirmed the validity of their genus-level classification in terms of three names they proposed. Taking an ultra-conservative position, Oliver et al. (2007) split Diplodactylus Gray 1832 sensu lato into three genera, using the first available names of Diplodactylus Gray 1832, Lucasium Wermuth, 1965 and Rhynchoedura Günther, 1867 for three main groups that diverged from one another in excess of 20 MYA.