Creating Ponds for Amphibians and Reptiles
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A Very European Tale – Britain Still Has Only Three Snake Species, but Its Grass Snake Is Now Assigned to Another Species (Natrix Helvetica)
SHORT COMMUNICATION The Herpetological Bulletin 141, 2017: 44-45 A very European tale – Britain still has only three snake species, but its grass snake is now assigned to another species (Natrix helvetica) UWE FRITZ1* & CAROLIN KINDLER1 1Senckenberg Natural History Collections Dresden, Museum of Zoology, A. B. Meyer Building, 01109 Dresden, Germany *Corresponding author Email: [email protected] ollowing several investigations of the phylogeography and systematics of grass snakes (Fritz et al., 2012; FKindler et al., 2013, 2014; Pokrant et al., 2016), we published a further detailed study on this topic in August (Kindler et al., 2017). Our new investigation revealed that only very limited gene flow occurs between western barred grass snakes and eastern common grass snakes. Consequently, we concluded that the barred grass snake (Fig. 1), previously a subspecies, should be elevated to a full species. August being the ‘silly season’ for news stories led the local media, including the highly respected BBC, to claim that Britain has now an additional snake species, i.e. four instead of three species – the northern viper (Vipera Figure 1. Young N. helvetica showing the distinctive lateral bars berus), the smooth snake (Coronella austriaca) as well as from which the species common name the ‘barred grass snake’ is derived (photo: © Jason Steel) two species of grass snake, the common grass snake (Natrix natrix) and the newly recognised barred grass snake (Natrix helvetica). findings. However, some southern populations identified This upheaval resulted from a complete misunderstanding by Thorpe with barred grass snakes, for instance from of a press release by the Senckenberg Institution. The press northern Italy, turned out to be distinct from N. -
<I>Ichthyosaura Alpestris</I>
Volume 26 (January 2016), 49–56 FULL PAPER Herpetological Journal Published by the British Provenance of Ichthyosaura alpestris (Caudata: Herpetological Society Salamandridae) introductions to France and New Zealand assessed by mitochondrial DNA analysis Jan W. Arntzen1, Tania M. King2, Mathieu Denoël3, Iñigo Martínez-Solano4,5 & Graham P. Wallis2 1Naturalis Biodiversity Center, PO Box 9517, 2300 RA Leiden, The Netherlands 2Department of Zoology, University of Otago, PO Box 56, Dunedin 9054, New Zealand 3Behavioural Biology Unit, Department of Biology, Ecology and Evolution, University of Liège, Quai van Beneden 22, 4020 Liège, Belgium 4CIBIO-InBIO, Centro de Investigação em Biodiversidade e Recursos Genéticos, Campus Agrário de Vairão, Universidade do Porto, Rua Padre Armando Quintas, s/n 4485-661 Vairão, Portugal 5(present address) Ecology, Evolution, and Development Group, Department of Wetland Ecology, Doñana Biological Station, CSIC, c/ Americo Vespucio, s/n, 41092, Seville, Spain The last century has seen an unparalleled movement of species around the planet as a direct result of human activity, which has been a major contributor to the biodiversity crisis. Amphibians represent a particularly vulnerable group, exacerbated by the devastating effects of chytrid fungi. We report the malicious translocation and establishment of the alpine newt (Ichthyosaura alpestris) to its virtual antipode in North Island of New Zealand. We use network analysis of mitochondrial DNA haplotypes to identify the original source population as I. a. apuana from Tuscany, Italy. Additionally, a population in southern France, presumed to be introduced, is identified as I. a. alpestris from western Europe. However, the presence of two differentiated haplotypes suggests a mixed origin. -
Phalangeal Bone Anomalies in the European Common Toad Bufo Bufo from Polluted Environments
Environ Sci Pollut Res DOI 10.1007/s11356-016-7297-6 RESEARCH ARTICLE Phalangeal bone anomalies in the European common toad Bufo bufo from polluted environments Mikołaj Kaczmarski1 & Krzysztof Kolenda 2 & Beata Rozenblut-Kościsty2 & Wioletta Sośnicka 2 Received: 7 March 2016 /Accepted: 20 July 2016 # The Author(s) 2016. This article is published with open access at Springerlink.com Abstract Every spring, many of amphibians are killed by ximately 20 % from the rural and semi-urban sites. In partic- motor vehicles on roads. These road-killed animals can be ular, we found hypertrophic bone cells, misaligned intercellu- used as valuable material for non-invasive studies showing lar substance, and irregular outer edges of bones. We suggest the effect of environmental pollution on amphibian popula- that these malformations are caused by different pollution, e.g. tions. The aims of our research were to check whether the with heavy metals. phalanges of road-killed toads may be useful as material for histological analysis, and whether various degrees of human Keywords Amphibians . Phalangeal bone . Poland . impact influence the level in bone abnormalities in the com- Pollution . Roadkilling . Skeletochronology . Urban area mon toad. We also examined whether the sex and age struc- ture of toads can differ significantly depending in the different sites. We chose three toad breeding sites where road-killed Introduction individuals had been observed: near the centre of a city, the outskirts of a city, and a rural site. We collected dead individ- Current knowledge widely indicates a direct relationship be- uals during spring migration in 2013. The sex of each individ- tween anthropogenic pressures and the deteriorating environ- ual was determined and the toes were used to determine age mental state and/or global extinction of amphibian popula- using the skeletochronology method. -
Toads Have Warts... and That's Good! | Nature Detectives | Summer 2021
Summer 2021 TOADS HAVE WARTS…AND THAT’S GOOD! Warts on your skin are not good. Warts can occur when a virus sneaks into human skin through a cut. A medicine gets rid of the virus and then it’s good-bye ugly wart. Toad warts look slightly like human warts, but toad warts and people warts are not one bit the same. Toad warts are natural bumps on a toad’s back. Toads have larger lumps behind their eyes. The bumps and lumps are glands. The glands produce a whitish goo that is a foul-tasting and smelly poison. The poison is a toad’s ultimate defense in a predator attack. It is toxic enough to kill small animals, if they swallow enough of it. The toxin can cause skin and eye irritation in humans. Some people used to think toad warts were contagious. Touching a toad can’t cause human warts, but licking a toad might make you sick! Toads have other defenses too. Their camouflage green/gray/brown colors blend perfectly into their surroundings. They can puff up with air to look bigger, and maybe less appetizing. Pull Out and Save Pull Out and Pick one up, and it might pee on your hand. Toads Travel, Frogs Swim Toads and frogs are amphibians with some similarities and quite a few differences. Amphibians spend all or part of their life in water. Frogs have moist, smooth skin that loses moisture easily. A toad’s dry, bumpy skin doesn’t lose water as easily as frog skin. Frogs are always in water or very near it, otherwise they quickly dehydrate and die. -
Common Frog Rana Temporaria
Common frog Rana temporaria Description Common frogs are common, widespread and easily recognisable amphibians. They have smooth, moist skin and long stripy legs. Common frogs are usually olive-green, although their colouration can be variable (from brown, yellow, cream or black, to pink, red, or lime-green). They have a dark patch (‘mask’) around the eye and eardrum, and often have other irregular black blotches over their body and limbs. They have large golden eyes with oval horizontal pupils. Frogs hop and jump rather than walk or crawl, and they are most active at night. They hibernate during the winter in pond mud or under piles of rotting leaves, logs or stones. Outside the breeding season, frogs are largely terrestrial and can be found in meadows, gardens and woodland. Breeding takes place in ponds, lakes, canals, and even wet grassland or puddles! Spawning usually occurs in January in the milder areas of the UK, but not until March to April in the North or upland areas. Mating pairs and masses of clumpy frogspawn can often be seen in waterbodies during this time. The eggs hatch into tadpoles within two to three weeks. What they eat Adult frogs eat snails, slugs, worms, insects and other invertebrates caught using their long sticky tongue. Young tadpoles feed on algae, but become carnivorous as they mature. Where and when to see them z Frogs can be spotted in ponds, lakes, canals, meadows, woodlands and gardens most commonly between February and October. z Look for frogspawn just below the surface of the water. Frogs lay a mass of jelly-like eggs, whereas toadspawn is produced in long strings. -
Amphibians and Reptiles in South Wales the Difference Between Amphibians and Reptiles
Amphibians & Reptiles i n S o u t h W a l e s ! ! ! ! ENVT0836 Amphibians and Reptiles in South Wales The difference between Amphibians and Reptiles Grass Snake © SWWARG Amphibians and reptiles are two ancient ! groups of animals that have been on the Smooth Newt © ARC planet for a very long time. The study of amphibians and reptiles is known as Amphibians, such as frogs, toads and ! Herpetology. To simplify matters, both newts, possess a porous skin that, when groups of animals will be referred to moist, exchanges oxygen meaning they throughout this booklet collectively as breathe through their skin. All amphibian Herpetofauna. Examples of both groups species in South Wales have to return to of animals live throughout South Wales water for breeding purposes. Adult and display a fascinating range of amphibians lay spawn in fresh water behaviour and survival tactics. bodies which then hatch and pass through a larval or tadpole stage prior to Common Lizard- female © SWWARG metamorphosing into miniature versions of the adults. • Generally possess smooth, moist skin • Generally slow moving Herpetofauna populations in South Wales • Generally in or around water are under ever increasing pressure due to a variety of reasons such as habitat loss, Common Toad © SWWARG colony isolation and human encroachment. There are many ways in which we can assist this group of misunderstood animals, which this booklet will attempt to highlight so that the reader can make their own valuable contribution towards helping to conserve both the animals and their habitat. ! page one Reptiles such as snakes and lizards, like amphibians, are cold blooded or ectotherms. -
Red-Spotted Newt Fact Sheet
WILDLIFE IN CONNECTICUT WILDLIFE FACT SHEET DENNIS QUINN Eastern Red-spotted Newt Notophthalmus v. viridescens Background and Range The red-spotted newt (also commonly referred to as the eastern newt) is widespread and familiar in many areas of Connecticut. Newts have four distinct life stages: egg, aquatic larvae, terrestrial juvenial (or “eft”), and aquatic adult. Their life cycle is one of the most complex of all the salamanders; starting as an egg, hatching into a larvae with external gills, then migrating to terrestrial habitats as juveniles where gills are replaced with lungs, and returning a few years later to their aquatic habitats as adults which retain their lungs. In Connecticut, the newt is found statewide, but more prominently west of the Connecticut River. The red-spotted newt has many subspecies and an extensive range throughout the United States. Description The adult red-spotted newt has smooth skin that is overall greenish in color, with small black dots scattered on the back and a row of several black-bordered reddish-orange spots on each side of the back. Male newts have black rough patches on the inside of their thighs and on the bottom tip of their hind toes during the breeding season. Adult newts are usually 3 to 5 inches in length. The juvenile, or eft, stage of the red-spotted newt is bright orange in color with small black dots scattered on the back and a row of larger, black-bordered orange spots on each side of the back. The skin is rough and dry compared to the moist and smooth skin of adults and larvae. -
Early Onset of Breeding Season in the Green Toad Bufotes Viridis in Western Poland
Herpetozoa 32: 109–112 (2019) DOI 10.3897/herpetozoa.32.e35825 Early onset of breeding season in the green toad Bufotes viridis in Western Poland Mikołaj Kaczmarski1, Klaudia Szala1, Janusz Kloskowski1 1 Poznan University of Life Sciences, Institute of Zoology, Wojska Polskiego 71c, 60-625, Poznań, Poland http://zoobank.org/083A67C2-D89B-4631-BFEC-D610D396E68F Corresponding author: Mikołaj Kaczmarski ([email protected]) Academic editor: Andreas Maletzky ♦ Received 29 July 2018 ♦ Accepted 9 January 2019 ♦ Published 22 May 2019 Abstract Amphibians are highly sensitive to environmental changes such as climate warming. Here, we report unusually early oviposition in two spatially isolated urban subpopulations of the green toad Bufotes viridis Laurenti, 1768, in Poznań, Western Poland. To our knowledge, we report the earliest breeding date for Central and Eastern Europe, for areas of similar latitude. We ascribe the early onset of B. viridis reproduction to an exceptionally warm spring in Western Poland in 2017. B. viridis shows flexibility in the timing of reproductive activity, however, shifts in breeding phenology may have both beneficial and detrimental population consequences. Key Words Amphibia, Anura, climate change, global warming, phenology, Poznań Global warming affects the phenology of amphibians (e.g. 2017): Park Cytadela [52°25'26"N, 16°55'56"E], a stone Beebee 1995; Muths et al. 2017), inducing shifts in repro- garden/amphitheatre with a permanent shallow concrete ductive periods that may influence amphibian populations pond (area: ca. 5,150 m2) and Park Rataje [52°23'9"N, both directly (e.g. mortality rates) and indirectly (e.g. im- 16°57'20"E], a post-industrial area containing debris and pacts on terrestrial and aquatic habitats, changes in food concrete waste, where, due to a non-permeable clay sub- webs or the spread of diseases) (Blaustein et al. -
A Nephroblastoma in a Fire-Bellied Newt, Cynops Pyrrhogaster1
[CANCER RESEARCH 30, 2691-2694, November 1970] A Nephroblastoma in a Fire-bellied Newt, Cynops pyrrhogaster1 P. Zwart Department for Exotic Animals, Veterinary Faculty, Biltstraat 172, Utrecht, The Netherlands SUMMARY According to the owner, this animal was imported from China via Hongkong, and it appeared to be in good condi A large intraabdominal tumor, consisting of renal blasto- tion at the time of purchase, 6 weeks prior to presentation. matous cells, early defective stages of glomerules, and undif- During the preceding few weeks, the animal had lost ferentiated tubular structures is described in a fully grown appetite, and become very thin and sluggish in its move female fire-bellied newt (Cynops pyrrhogaster). Questions of ments; recently, it had developed a posterior paralysis. Upon nomenclature of renal embryonal tumors in lower vertebrates inspection, the newt appeared emaciated; the movements of are briefly discussed. The tumor is designated a nephro- the hind legs were hampered by a large swelling within the blastoma. abdomen, which dorsally distended the left flank. A firm mass with an irregular surface giving the impression of INTRODUCTION multiloculated, pea-sized cysts was palpable; it appeared to Nephroblastomas seem to be very rare in animals with be adherent to the abdominal wall. A few drops of a watery mesonephritic kidneys (fishes and amphibia), although fluid were obtained on aspiration. In view of the poor immense numbers of many species are kept as pets and in condition of the animal, the rapid development of the laboratories. A single case was recorded in the steelhead disease, and the extent of the swelling, the prognosis was trout (5). -
Italian Crested Newt – Triturus Carnifex Laurenti, 1768 (Amphibia, Caudata, Salamandridae, Pleurodelinae) in the Batrachofauna of Bosnia and Herzegovina
Short Note Hyla VOL. 2015., No.2, pp. 52 - 55 ISSN: 1848-2007 Zimić & Šunje Italian crested newt – Triturus carnifex Laurenti, 1768 (Amphibia, Caudata, Salamandridae, Pleurodelinae) in the batrachofauna of Bosnia and Herzegovina 1 1,2,* ADNAN ZIMIĆ & EMINA ŠUNJE 1Herpetological Association in Bosnia and Hercegovina "ATRA", Sarajevo, B&H 2Faculty of Natural Sciences and Mathematics. Zmaja od Bosne 33-35, Sarajevo, B&H *Corresponding author: [email protected] Bosnia and Herzegovina (B&H) has a high finally elevated to the species level (ARNTZEN et al., biogeographic importance for Balkan batrachofauna 2007; FROST, 2015). Old literature data (e.g. BOLKAY, biodiversity with 12 amphibian chorotypes (JABLONSKI 1929) mentioning T. carnifex in B&H should be treated et al., 2012) and 20 amphibian species (LELO & VESNIĆ, as findings of Triturus macedonicus (Figure 1). 2011; ĆURIĆ & ZIMIĆ, 2014; FROST, 2015). Hereby we Morphologically the three species belonging to the genus present the first official record of the 21st species known Triturus [T. dobrogicus (KIRITZESCU, 1903), T. carnifex for the B&H batrachofauna: Triturus carnifex LAURENTI, (LAURENTI, 1768) and T. macedonicus (KARAMAN, 1768. 1922)] can be distinguished by coloration and spotting During a long amphibian research period in pattern, Wolterstorff index – WI and Number of Rib- B&H (from: MÖELLENDORFF, 1873 – till present), T. Bearing Vertebrae – NRBV (WIELSTRA & ARNTZEN, carnifex has actually never been officially listed in the 2011; ARNTZEN et al., 2015). B&H fauna for two main reasons: (a) although it has From May 25 – 27. 2015, three females and one been known that the species occurs in the northwestern male of T. -
From Montenegro
Correspondence ISSN 2336-9744 (online) | ISSN 2337-0173 (print) The journal is available on line at www.ecol-mne.com Melanism in Natrix natrix and Natrix tessellata (Serpentes: Colubridae) from Montenegro SLA ĐANA GVOZDENOVI Ć1* and MARIO SCHWEIGER 2 1 Montenegrin Ecologist Society, Bulevar Sv. Petra Cetinjskog 73, Podgorica, Montenegro. *Corresponding author. E-mail: [email protected] 2 Vipersgarden, Katzelsberg 4, 5162 Obertrum, Ӧsterreich. E-mail: [email protected] Received 13 November 2014 │ Accepted 10 December 2014 │ Published online 11 December 2014. The coloration in animals plays an important role in predator avoidance (Sweet 1985), inter- and intraspecific communication and sexual selection (Roulin & Bize 2006). Different color morphs occur in many reptiles, and the most frequent one is melanism, especially in snakes (Lorioux et al . 2008). There exist few advantages of this phenomen as: faster heating rates, higher mean body temperatures, protection from overheating (Luiselli 1992; Forsman 1995; Bittner et al . 2002; Tanaka 2005; Clusella-Trullas et al . 2008), but also disadvantages, such as higher predation risk (Clusella-Trullas et al., 2008). Melanism in European snakes has been reported for: Zamenis longissimus , Hierophis viridiflavus , Coronella austriaca , Platyceps najadum , Natrix maura , Natrix natrix , Natrix tessellata , Vipera berus , Vipera aspis (Terhivuo 1990; Cattaneo 2003; Zuffi 2008; Pernetta & Reading 2009; Strugariu & Zamfirescu 2009; Zadravec & Lauš 2011; Mollov 2012; Ajti ć et al . 2013). Figures 1-2. Left (Fig. 1): Black dice snake Natrix tessellata from river Bojana, Ulcinj. Right (Fig. 2): Black grass snake Natrix natrix persa from Tanki rt, Skadar Lake Ecol. Mont., 1 (4), 2014, 231-233 231 MELANISM IN NATRIX NATRIX AND N.TESSELLATA FROM MONTENEGRO In this paper we present melanism in two species: Natrix natrix (Linnaeus, 1758) and Natrix tessellata (Laurenti, 1768) from Montenegro. -
Missouri's Toads and Frogs Booklet
TOADSMissouri’s andFROGS by Jeffrey T. Briggler and Tom R. Johnson, Herpetologists www.MissouriConservation.org © 1982, 2008 Missouri Conservation Commission Equal opportunity to participate in and benefit from programs of the Missouri Department of Conservation is available to all individuals without regard to their race, color, national origin, sex, age or disability. Questions should be directed to the Department of Conservation, P.O. Box 180, Jefferson City, MO 65102, (573) 751-4115 (voice) or 800-735-2966 (TTY), or to the U.S. Fish and Wildlife Service Division of Federal Assistance, 4401 N. Fairfax Drive, Mail Stop: MBSP-4020, Arlington, VA 22203. Cover photo: Eastern gray treefrog by Tom R. Johnson issouri toads and frogs are colorful, harmless, vocal and valuable. Our forests, prairies, rivers, swamps and marshes are Mhome to a multitude of toads and frogs, but few people know how many varieties we have, how to tell them apart, or much about their natural history. Studying these animals and sharing their stories with fellow Missourians is one of the most pleasurable and rewarding aspects of our work. Toads and frogs are amphibians—a class Like most of vertebrate animals that also includes amphibians, salamanders and the tropical caecilians, which are long, slender, wormlike and legless. frogs and Missouri has 26 species and subspecies (or toads have geographic races) of toads and frogs. Toads and frogs differ from salamanders by having an aquatic relatively short bodies and lacking tails at adulthood. Being an amphibian means that tadpole stage they live two lives: an aquatic larval or tadpole and a semi- stage and a semi-aquatic or terrestrial adult stage.