HERPETOLOJİ (Ders Kitabı)
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A Review of Southern Iraq Herpetofauna
Vol. 3 (1): 61-71, 2019 A Review of Southern Iraq Herpetofauna Nadir A. Salman Mazaya University College, Dhi Qar, Iraq *Corresponding author: [email protected] Abstract: The present review discussed the species diversity of herpetofauna in southern Iraq due to their scientific and national interests. The review includes a historical record for the herpetofaunal studies in Iraq since the earlier investigations of the 1920s and 1950s along with the more recent taxonomic trials in the following years. It appeared that, little is known about Iraqi herpetofauna, and no comprehensive checklist has been done for these species. So far, 96 species of reptiles and amphibians have been recorded from Iraq, but only a relatively small proportion of them occur in the southern marshes. The marshes act as key habitat for globally endangered species and as a potential for as yet unexplored amphibian and reptile diversity. Despite the lack of precise localities, the tree frog Hyla savignyi, the marsh frog Pelophylax ridibunda and the green toad Bufo viridis are found in the marshes. Common reptiles in the marshes include the Caspian terrapin (Clemmys caspia), the soft-shell turtle (Trionyx euphraticus), the Euphrates softshell turtle (Rafetus euphraticus), geckos of the genus Hemidactylus, two species of skinks (Trachylepis aurata and Mabuya vittata) and a variety of snakes of the genus Coluber, the spotted sand boa (Eryx jaculus), tessellated water snake (Natrix tessellata) and Gray's desert racer (Coluber ventromaculatus). More recently, a new record for the keeled gecko, Cyrtopodion scabrum and the saw-scaled viper (Echis carinatus sochureki) was reported. The IUCN Red List includes six terrestrial and six aquatic amphibian species. -
Cryptic Speciation Patterns in Iranian Rock Lizards Uncovered by Integrative Taxonomy
Cryptic Speciation Patterns in Iranian Rock Lizards Uncovered by Integrative Taxonomy Faraham Ahmadzadeh1,2*, Morris Flecks2, Miguel A. Carretero3, Omid Mozaffari4, Wolfgang Bo¨ hme2,D. James Harris3, Susana Freitas3, Dennis Ro¨ dder2 1 Department of Biodiversity and Ecosystem Management, Environmental Sciences Research Institute, Shahid Beheshti University, Tehran, Iran, 2 Zoologisches Forschungsmuseum Alexander Koenig, Bonn, Germany, 3 Centro de Investigac¸a˜o em Biodiversidade e Recursos Gene´ticos, Universidade do Porto, Vaira˜o, Porto, Portugal, 4 Aria Herpetological Institute, Tehran, Iran Abstract While traditionally species recognition has been based solely on morphological differences either typological or quantitative, several newly developed methods can be used for a more objective and integrative approach on species delimitation. This may be especially relevant when dealing with cryptic species or species complexes, where high overall resemblance between species is coupled with comparatively high morphological variation within populations. Rock lizards, genus Darevskia, are such an example, as many of its members offer few diagnostic morphological features. Herein, we use a combination of genetic, morphological and ecological criteria to delimit cryptic species within two species complexes, D. chlorogaster and D. defilippii, both distributed in northern Iran. Our analyses are based on molecular information from two nuclear and two mitochondrial genes, morphological data (15 morphometric, 16 meristic and four categorical characters) and eleven newly calculated spatial environmental predictors. The phylogeny inferred for Darevskia confirmed monophyly of each species complex, with each of them comprising several highly divergent clades, especially when compared to other congeners. We identified seven candidate species within each complex, of which three and four species were supported by Bayesian species delimitation within D. -
Timon Lepidus (Daudin, 1802) Timon Lepidus (Daudin, 1802) Lézard Ocellé
Timon lepidus (Daudin, 1802) Timon lepidus (Daudin, 1802) Lézard ocellé Ecologie et statut de l'espèce Section révisée et complétée par Philippe Geniez. cd_ref 79273 Famille Lacertidae Aire de répartition mondiale : Le Lézard ocellé (Timon lepidus, anciennement connu sous le nom de Lacerta lepida fait partie d'un petit genre de la famille des Lacertidae comprenant six espèces, 4 distribuées dans l'ouest du bassin méditerranéen (le groupe de Timon lepidus) et deux dans l'est (groupe de Timon princeps). Sur la base de caractéristiques morphologiques (taille, coloration, forme des dents, etc.), trois sous-espèces sont actuellement retenues au sein de l'espèce lepidus bien que plusieurs auteurs ne les reconnaissent pas toutes : -Timon l. lepidus (Daudin 1802), occupe la majeure partie de la péninsule Ibérique, la moitié sud et l'ouest de la France jusqu'à l'extrême nord-ouest de l'Italie (Cheylan & Grillet 2004, 2005 ; Salvidio et al, 2004). -Timon l. ibericus López-Seoane, 1884 est localisé en Galice (nord-ouest de l’Espagne) et dans le nord du Portugal. -Timon l. oteroi Castroviejo & Matéo, 1998 concerne une population insulaire localisée sur l'île de Sálvora en Galice. Des études phylogénétiques récentes révèlent cependant l'existence de cinq lignées génétiquement et géographiquement bien distinctes au sein de la péninsule Ibérique dont l’une d’elle, la « lignée », la plus répandue, est celle qui est présente en France et en Italie (Miraldo et al., 2011). La sous-espèce oteroi apparaît comme une population insulaire présentant quelques caractéristiques morphologiques liée à l’insularité mais qui entre clairement dans la « lignée » (T. -
Evolution of Oviductal Gestation in Amphibians MARVALEE H
THE JOURNAL OF EXPERIMENTAL ZOOLOGY 266394-413 (1993) Evolution of Oviductal Gestation in Amphibians MARVALEE H. WAKE Department of Integrative Biology and Museum of Vertebrate Zoology, University of California,Berkeley, California 94720 ABSTRACT Oviductal retention of developing embryos, with provision for maternal nutrition after yolk is exhausted (viviparity) and maintenance through metamorphosis, has evolved indepen- dently in each of the three living orders of amphibians, the Anura (frogs and toads), the Urodela (salamanders and newts), and the Gymnophiona (caecilians). In anurans and urodeles obligate vivi- parity is very rare (less than 1%of species); a few additional species retain the developing young, but nutrition is yolk-dependent (ovoviviparity) and, at least in salamanders, the young may be born be- fore metamorphosis is complete. However, in caecilians probably the majority of the approximately 170 species are viviparous, and none are ovoviviparous. All of the amphibians that retain their young oviductally practice internal fertilization; the mechanism is cloaca1 apposition in frogs, spermato- phore reception in salamanders, and intromission in caecilians. Internal fertilization is a necessary but not sufficient exaptation (sensu Gould and Vrba: Paleobiology 8:4-15, ’82) for viviparity. The sala- manders and all but one of the frogs that are oviductal developers live at high altitudes and are subject to rigorous climatic variables; hence, it has been suggested that cold might be a “selection pressure” for the evolution of egg retention. However, one frog and all the live-bearing caecilians are tropical low to middle elevation inhabitants, so factors other than cold are implicated in the evolu- tion of live-bearing. -
Darevskia Raddei and Darevskia Portschinskii) May Not Lead to Hybridization Between Them
Zoologischer Anzeiger 288 (2020) 43e52 Contents lists available at ScienceDirect Zoologischer Anzeiger journal homepage: www.elsevier.com/locate/jcz Research paper Syntopy of two species of rock lizards (Darevskia raddei and Darevskia portschinskii) may not lead to hybridization between them * Eduard Galoyan a, b, , Viktoria Moskalenko b, Mariam Gabelaia c, David Tarkhnishvili c, Victor Spangenberg d, Anna Chamkina b, Marine Arakelyan e a Severtsov Institute of Ecology and Evolution, 33 Leninskij Prosp. 119071, Moscow, Russia b Zoological Museum, Lomonosov Moscow State University, Moscow, Russia c Center of Biodiversity Studies, Institute of Ecology, Ilia State University, Tbilisi, Georgia d Vavilov Institute of General Genetics, Russian Academy of Sciences, Moscow, Russia e Department of Zoology, Yerevan State University, Yerevan, Armenia article info abstract Article history: The two species of rock lizards, Darevsia raddei and Darevskia portschinskii, belong to two different Received 19 February 2020 phylogenetic clades of the same genus. They are supposed ancestors for the hybrid parthenogenetic, Received in revised form Darevskia rostombekowi. The present study aims to identify morphological features of these two species 22 June 2020 and the potential gene introgression between them in the area of sympatry. External morphological Accepted 30 June 2020 features provided the evidence of specific morphology in D. raddei and D. portschinskii: the species Available online 14 July 2020 differed in scalation and ventral coloration pattern, however, they had some proportional similarities Corresponding Editor: Alexander Kupfer within both sexes of the two species. Males of both species had relatively larger heads and shorter bodies than females. Males of D. raddei were slightly larger than males of D. -
Nectophrynoides Tornieri (Anura: Bufonidae) in the Amani Nature Reserve, Tanzania“
DIPLOMARBEIT Titel der Diplomarbeit „The „push-up“ as a calling posture in Nectophrynoides tornieri (Anura: Bufonidae) in the Amani Nature Reserve, Tanzania“ Verfasserin Iris Starnberger angestrebter akademischer Grad Magistra der Naturwissenschaften (Mag.rer.nat.) Wien, 2011 Studienkennzahl lt. A 439 Studienblatt: Studienrichtung lt. Diplomstudium Zoologie (Stzw) UniStG Studienblatt: Betreuerin / Betreuer: Ao. Univ.-Prof. Mag. Dr. Walter Hödl Für meine Eltern und meine Schwester Sonja, die mich immer liebevoll unterstützt und ermutigt haben. 2 Table of Contents INTRODUCTION .............................................................................................................................................4 MATERIALS AND METHODS.......................................................................................................................8 STUDY SITE ......................................................................................................................................................................... 8 EXPERIMENTAL DESIGN ................................................................................................................................................... 8 HABITAT FEATURES....................................................................................................................................................... 10 DATA ANALYSIS ............................................................................................................................................................. -
E-Program DO NOT PRINT!
e-program DO NOT PRINT! You’ll receive a pocket program at registration, so no need to print this one. This e-program includes all presentation sessions and the associated abstracts, which are hyperlinked to the name of the presenter. Plenary abstracts are included in the pocket program. The plan on a page Tuesday June 20 Wednesday June 21 Thursday June 22 Friday June 23 7:30-8:30 am Breakfast: 7:30-8:30am Breakfast: 7:30-8:30am Breakfast: Dining Hall Dining Hall Dining Hall 8:50-10:00am Plenary: 8:50-10:00am Plenary: 8:50-10:00am Plenary: Rick Sabrina Fossette-Halot - Renee Catullo - Chapel. Shine - Chapel. Introduced Chapel. Introduced by Nicki Introduced by Scott Keogh by Ben Philips Mitchell 10:00-10:25 am Tea break 10:00-10:15am Tea break 10:00-10:25am Tea break 10:30-11:54am Short 10:20am -12:00pm Mike Bull 10:30-11:42am Short Talks: Talks: Session 1 - Symposium - Chapel Session 8 - Clubhouse: Clubhouse: upstairs and upstairs and downstairs downstairs 11:45 Conference close (upstairs) 12:00-2:00pm Lunch 12:00-1:00pm Conference 12:00-1:00pm Lunch: Dining (Dining Hall) and ASH photo and lunch Hall or Grab and Go, buses AGM (Clubhouse upstairs) depart for airport from midday High ropes course and 1:00-2:00pm Short Talks: climbing wall open. Book at Session 5 - Clubhouse: registration on Tuesday if upstairs and downstairs interested 2:00 -4:00pm 2:00-3:00pm Speed talks: 2:00-3:00pm Speed talks: Registration, locate Session 2 Clubhouse Session 6 Clubhouse accommodation, light upstairs upstairs fires, load talks, book activities 3:00-3:25pm -
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Tarkhnishvili et al. BMC Evolutionary Biology (2020) 20:122 https://doi.org/10.1186/s12862-020-01690-9 RESEARCH ARTICLE Open Access Genotypic similarities among the parthenogenetic Darevskia rock lizards with different hybrid origins David Tarkhnishvili1* , Alexey Yanchukov2, Mehmet Kürşat Şahin3, Mariam Gabelaia1, Marine Murtskhvaladze1, Kamil Candan4, Eduard Galoyan5, Marine Arakelyan6, Giorgi Iankoshvili1, Yusuf Kumlutaş4, Çetin Ilgaz4, Ferhat Matur4, Faruk Çolak2, Meriç Erdolu7, Sofiko Kurdadze1, Natia Barateli1 and Cort L. Anderson1 Abstract Background: The majority of parthenogenetic vertebrates derive from hybridization between sexually reproducing species, but the exact number of hybridization events ancestral to currently extant clonal lineages is difficult to determine. Usually, we do not know whether the parental species are able to contribute their genes to the parthenogenetic vertebrate lineages after the initial hybridization. In this paper, we address the hypothesis, whether some genotypes of seven phenotypically distinct parthenogenetic rock lizards (genus Darevskia) could have resulted from back-crosses of parthenogens with their presumed parental species. We also tried to identify, as precise as possible, the ancestral populations of all seven parthenogens. Results: We analysed partial mtDNA sequences and microsatellite genotypes of all seven parthenogens and their presumed ansectral species, sampled across the entire geographic range of parthenogenesis in this group. Our results confirm the previous designation of the parental species, but further specify the maternal populations that are likely ancestral to different parthenogenetic lineages. Contrary to the expectation of independent hybrid origins of the unisexual taxa, we found that genotypes at multiple loci were shared frequently between different parthenogenetic species. The highest proportions of shared genotypes were detected between (i) D. -
Body-Size Effect on Egg Size in Eublepharid Geckos (Squamata
Blackwell Publishing LtdOxford, UKBIJBiological Journal of the Linnean Society0024-4066The Linnean Society of London, 20062006 884 527532 Original Article EGG-SIZE ALLOMETRY IN EUBLEPHARID GECKOS L. KRATOCHVÍL and D. FRYNTA Biological Journal of the Linnean Society, 2006, 88, 527–532. With 2 figures Body-size effect on egg size in eublepharid geckos (Squamata: Eublepharidae), lizards with invariant clutch size: negative allometry for egg size in ectotherms is not universal LUKÁT KRATOCHVÍL1* and DANIEL FRYNTA2 1Department of Ecology, Charles University, Vinidná 7, CZ-128 44 Praha 2, the Czech Republic 2Department of Zoology, Charles University, Vinidná 7, CZ-128 44 Praha 2, the Czech Republic Received 1 February 2005; accepted for publication 5 December 2005 Within a single clutch, smaller species of ectotherms generally lay a smaller number of relatively larger eggs than do larger species. Many hypotheses explaining both the interspecific negative allometry in egg size and egg size– number trade-off postulate the existence of an upper limit to the egg size of larger species. Specifically, in lizards, large eggs of large species could have too long a duration of incubation, or they could be too large to pass through the pelvic opening, which is presumably constrained mechanically in larger species. Alternatively, negative allometry could be a result of limits affecting eggs of smaller species. Under the latter concept, hatchling size in smaller species may be close to the lower limit imposed by ecological interactions or physiological processes, and therefore smaller species have to invest in relatively larger offspring. Contrary to these lower limit hypotheses, explanations based on the existence of an upper limit always predict negative egg-size allometry even in animals with invariant clutch size, in which naturally there is no egg size–number trade-off. -
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. -
Species List of Amphibians and Reptiles from Turkey
Journal of Animal Diversity Online ISSN 2676-685X Volume 2, Issue 4 (2020) http://dx.doi.org/10.29252/JAD.2020.2.4.2 Review Article Species list of Amphibians and Reptiles from Turkey Muammer Kurnaz Gümüşhane University, Kelkit Vocational School of Health Services, Department of Medical Services and Techniques 29600, Kelkit / Gümüşhane, Turkey *Corresponding author : [email protected] Abstract Turkey is biogeographically diverse and consequently has a rich herpetofauna. As a result of active herpetological research, the number of species has steadily increased in recent years. I present here a new checklist of amphibian and reptile species distributed in Turkey, revising the nomenclature to reflect the latest taxonomic knowledge. In addition, information about the systematics of many species is also given. In total 35 (19.4%) amphibian and 145 Received: 8 October 2020 (80.6%) reptile species comprise the Turkish herpetofauna. Among amphibians, 16 (45.7%) Accepted: 23 December 2020 anurans and 19 urodelans (54.3%) are present. Among reptiles, 11 (7.6%) testudines, 71 Published online: 31 January 2021 (49%) saurians, 3 (2.1%) amphisbaenians and 60 (41.3%) ophidians are considered part of the herpetofauna. The endemism rate in Turkey is considered relatively high with a total of 34 species (12 amphibian species – 34.3% and 22 reptile species – 15.2%) endemic to Turkey, yielding a total herpetofaunal endemism of 18.9%. While 38 species have not been threat-assessed by the IUCN, 92 of the 180 Turkish herpetofaunal species are of Least Concern (LC), 13 are Near Threatened (NT), 10 are Vulnerable (VU), 14 are Endangered (EN), and 7 are Critically Endangered (CR). -
Biodiversity Profile of Afghanistan
NEPA Biodiversity Profile of Afghanistan An Output of the National Capacity Needs Self-Assessment for Global Environment Management (NCSA) for Afghanistan June 2008 United Nations Environment Programme Post-Conflict and Disaster Management Branch First published in Kabul in 2008 by the United Nations Environment Programme. Copyright © 2008, United Nations Environment Programme. This publication may be reproduced in whole or in part and in any form for educational or non-profit purposes without special permission from the copyright holder, provided acknowledgement of the source is made. UNEP would appreciate receiving a copy of any publication that uses this publication as a source. No use of this publication may be made for resale or for any other commercial purpose whatsoever without prior permission in writing from the United Nations Environment Programme. United Nations Environment Programme Darulaman Kabul, Afghanistan Tel: +93 (0)799 382 571 E-mail: [email protected] Web: http://www.unep.org DISCLAIMER The contents of this volume do not necessarily reflect the views of UNEP, or contributory organizations. The designations employed and the presentations do not imply the expressions of any opinion whatsoever on the part of UNEP or contributory organizations concerning the legal status of any country, territory, city or area or its authority, or concerning the delimitation of its frontiers or boundaries. Unless otherwise credited, all the photos in this publication have been taken by the UNEP staff. Design and Layout: Rachel Dolores