Salamanders of Rhode Island Red-Backed Salamanders Are a Common and Plentiful Am- Not Yet Widespread
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Kentucky Salamanders of the Genus Desmognathus: Their Identification, Distribution, and Morphometric Variation
KENTUCKY SALAMANDERS OF THE GENUS DESMOGNATHUS: THEIR IDENTIFICATION, DISTRIBUTION, AND MORPHOMETRIC VARIATION A Thesis Presented to the Faculty of the College of Science and Technology Morehead State University In Partial Fulfilhnent of the Requirements for the Degree Master of Science in Biology by Leslie Scott Meade July 24, 2000 1CAMDElJ CARROLL LIBRARY MOREHEAD, KY 40351 f'\Sl.l 11-feSfS 5q7,g'5' M 'ff I k Accepted by the Faculty of the College of Science and Technology, Morehead State University, in partial fulfillment ofthe requirements for the Master of Science Degree. ~ C ~ Director of Thesis Master's Committee: 7, -.2't-200c) Date 11 Kentucky Salamanders of the Genus Desmognathus: Their Identification, Distribution, and Morphometric Variation The objectives of this study were to ( 1) summarize the taxonomic and natural history data for Desmognathus in Kentucky, (2) compare Kentucky species and sub species of Desmognathus with regard to sexual dimorphism, (3) analyze interspecific variation in morphology of Kentucky Desmognathus, and (4) compile current range maps for Desmognathus in Kentucky. Species and subspecies examined included D. ochrophaeus Cope (Allegheny Mountain Dusky Salamander), D. fuscus fuscus (Green) (Northern Dusky Salamander), D. fuscus conanti Rossman (Spotted Dusky Salamander), D. montico/a Dunn (Seal Salamander), and D. welteri Barbour (Black Mountain Dusky Salamander). Salamanders were collected in the field or borrowed from museum collections. Taxonomic and natural history data for Kentucky Desmo gnathus were compiled from literature, preserved specimens, and direct observations. Morphometric characters examined included total length, snout-vent length, tail length, head length, head width, snout length, vent length, tail length/total length, snout-vent length/total length, and snout length/head length. -
<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. -
Spotted Salamander (Ambystoma Maculafum)
Spotted Salamander (Ambystoma maculafum) RANGE: Nova Scotia and the Gaspe Peninsula to s. On- BREEDINGPERIOD: March to mid-April. Mass breeding tario, s. through Wisconsin, s. Illinois excluding prairie migrations occur in this species: individuals enter and regions, toe. Kansas andTexas, and through the Eastern leave breeding ponds using the same track each year, United States, except Florida, the Delmarva Peninsula, and exhibit fidelity to breeding ponds (Shoop 1956, and s. New Jersey. 1974). Individuals may not breed in consecutive years (Husting 1965). Breeding migrations occur during RELATIVE ABUNDANCEIN NEW ENGLAND:Common steady evening rainstorms. though populations declining, probably due to acid pre- cipitation. EGG DEPOSITION:1 to 6 days after first appearance of adults at ponds (Bishop 1941 : 114). HABITAT:Fossorial; found in moist woods, steambanks, beneath stones, logs, boards. Prefers deciduous or NO. EGGS/MASS:100 to 200 eggs, average of 125, laid in mixed woods on rocky hillsides and shallow woodland large masses of jelly, sometimes milky, attached to stems ponds or marshy pools that hold water through the sum- about 15 cm (6 inches) under water. Each female lays 1 to mer for breeding. Usually does not inhabit ponds con- 10 masses (average of 2 to 3) of eggs (Wright and Allen taining fish (Anderson 1967a). Terrestrial hibernator. In 1909).Woodward (1982)reported that females breeding summer often wanders far from water source. Found in in permanent ponds produced smaller, more numerous low oak-hickory forests with creeks and nearby swamps eggs than females using temporary ponds. in Illinois (Cagle 1942, cited in Smith 1961 :30). -
The Natural History, Distribution, and Phenotypic Variation of Cave-Dwelling Spring Salamanders, Gyrinophilus Spp
Marshall University Marshall Digital Scholar Theses, Dissertations and Capstones 2005 The aN tural History, Distribution, and Phenotypic Variation of Cave-dwelling Spring Salamanders, Gyrinophilus spp. Cope (Plethodontidae), in West Virginia Michael Steven Osbourn Follow this and additional works at: http://mds.marshall.edu/etd Part of the Aquaculture and Fisheries Commons, and the Ecology and Evolutionary Biology Commons Recommended Citation Osbourn, Michael Steven, "The aN tural History, Distribution, and Phenotypic Variation of Cave-dwelling Spring Salamanders, Gyrinophilus spp. Cope (Plethodontidae), in West Virginia" (2005). Theses, Dissertations and Capstones. Paper 735. This Thesis is brought to you for free and open access by Marshall Digital Scholar. It has been accepted for inclusion in Theses, Dissertations and Capstones by an authorized administrator of Marshall Digital Scholar. For more information, please contact [email protected]. The Natural History, Distribution, and Phenotypic Variation of Cave-dwelling Spring Salamanders, Gyrinophilus spp. Cope (Plethodontidae), in West Virginia. Thesis submitted to The Graduate College of Marshall University In partial fulfillment of the Requirements for the degree of Master of Science Biological Sciences By Michael Steven Osbourn Thomas K. Pauley, Committee Chairperson Daniel K. Evans, PhD Thomas G. Jones, PhD Marshall University May 2005 Abstract The Natural History, Distribution, and Phenotypic Variation of Cave-dwelling Spring Salamanders, Gyrinophilus spp. Cope (Plethodontidae), in West Virginia. Michael S. Osbourn There are over 4000 documented caves in West Virginia, potentially providing refuge and habitat for a diversity of amphibians and reptiles. Spring Salamanders, Gyrinophilus porphyriticus, are among the most frequently encountered amphibians in caves. Surveys of 25 caves provided expanded distribution records and insight into ecology and diet of G. -
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. -
2008 Amphibian Distribution Surveys in Wadeable Streams and Ponds in Western and Southeast Oregon
INFORMATION REPORTS NUMBER 2010-05 FISH DIVISION Oregon Department of Fish and Wildlife 2008 Amphibian Distribution Surveys in Wadeable Streams and Ponds in Western and Southeast Oregon Oregon Department of Fish and Wildlife prohibits discrimination in all of its programs and services on the basis of race, color, national origin, age, sex or disability. If you believe that you have been discriminated against as described above in any program, activity, or facility, or if you desire further information, please contact ADA Coordinator, Oregon Department of Fish and Wildlife, 3406 Cherry Drive NE, Salem, OR, 503-947-6000. This material will be furnished in alternate format for people with disabilities if needed. Please call 541-757-4263 to request 2008 Amphibian Distribution Surveys in Wadeable Streams and Ponds in Western and Southeast Oregon Sharon E. Tippery Brian L. Bangs Kim K. Jones Oregon Department of Fish and Wildlife Corvallis, OR November, 2010 This project was financed with funds administered by the U.S. Fish and Wildlife Service State Wildlife Grants under contract T-17-1 and the Oregon Department of Fish and Wildlife, Oregon Plan for Salmon and Watersheds. Citation: Tippery, S. E., B. L Bangs and K. K. Jones. 2010. 2008 Amphibian Distribution Surveys in Wadeable Streams and Ponds in Western and Southeast Oregon. Information Report 2010-05, Oregon Department of Fish and Wildlife, Corvallis. CONTENTS FIGURES....................................................................................................................................... -
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. -
Dusky Salamander Desmognathus Fuscus
WILDLIFE IN CONNECTICUT WILDLIFE FACT SHEET PAUL J. FUSCO PAUL Dusky Salamander Desmognathus fuscus Background and Range The northern dusky salamander is in the lungless salamander family (Plethodontidae). This species was historically distributed widely in streams, springs, and seepage areas throughout Connecticut. However, it has become scarce in more developed areas of the state, especially in Fairfield, New Haven, and Hartford Counties. The northern dusky salamander ranges from south Quebec and southern New Brunswick, down the Appalachians to its southernmost point in mid-South Carolina. Its western extent reaches east Indiana and the eastern half of Kentucky. In Connecticut, it is found statewide but only sparsely in New London and Fairfield counties. Description This stout, medium-sized salamander exhibits variable brown coloration with mottling, and a translucent belly that has “salt and pepper” patterning. The tail is flattened laterally, with a knife-like top edge. A small white line runs from the jaw to the eye, and a groove goes from each nostril to the jaw edge. Hind legs are noticeably larger than forelimbs. Younger individuals have a greater range in color from olive to chestnut to dark tan. Larvae possess a few pairs of yellowish spots bordered with a dark, wavy lateral line that goes along the back. Larvae can be confused with the larger two-lined salamander; however, the two-lined has less pronounced rear limbs. Habitat and Diet The northern dusky is usually found in or near freshwater, such as streams, springs, and/or areas with seepage. CONNECTICUT DEPARTMENT OF ENERGY & ENVIRONMENTAL PROTECTION ● WILDLIFE DIVISION These sites tend to be associated with closed canopy deciduous or coniferous forests. -
Tail Bifurcation in a Northern Dusky Salamander, Desmognathus Fuscus (Caudata: Plethodontidae)
Herpetology Notes, volume 10: 181-182 (2017) (published online on 25 April 2017) Tail bifurcation in a Northern Dusky Salamander, Desmognathus fuscus (Caudata: Plethodontidae) Sean M. Hartzell1,* Tail bifurcation, a condition in which a portion of species Bolitoglossa heiroreias, Plethodon cinereus the tail duplicates after mechanical damage, typically and P. glutinosus (Henle et al., 2012; Medina-Florez resulting from attempted predation, is occasionally and Townsend, 2014). Henle et al. (2012) report no observed in lizards (e.g., Cordes and Walker, 2013; references concerning tail bifurcation in the genus Tamar et al., 2013; Passos et al., 2014; Pheasey et Desmognathus, suggesting the observation reported al., 2014). However, few reports have appeared in herein may be novel for D. fuscus and potentially the literature regarding tail bifurcations in natural for the genus Desmognathus. While the cause of tail populations of post-larval amphibians (Henle et al., bifurcation observed in the D. fuscus is unknown, likely, 2012). Henle et al. (2012) exhaustively reviewed the this arose from damage during a predation attempt, as literature and reported 19 references documenting post has been suggested in cases of tail bifurcation in other larval tail bifurcation in 13 salamander species among salamanders (Henle et al., 2012). eight genera (Ambystoma, Plethodon, Chioglossa, Cynops, Lissotriton, Notophthalmus, Salamandra, and Triturus). More recently, Medina-Florez and Townsend (2014) reported tail bifurcation in Bolitoglossa heiroreias. Herein, I report an observation of tail bifurcation in Desmognathus fuscus (Rafinesque, 1820) a semiaquatic salamander native to the eastern United States and portions of extreme southeastern Canada (Petranka, 1998). On 22 December 2016 at 1200 h, a young, post-larval Desmognathus fuscus (ca. -
Subterranean Reproduction of the Southern Two-Lined Salamander (Eurycea Cirrigera) from Short Mountain, Tennessee
Herpetological Conservation and Biology 2(2):106-112. Submitted: 15 April 2007; Accepted: 7 July 2007 SUBTERRANEAN REPRODUCTION OF THE SOUTHERN TWO-LINED SALAMANDER (EURYCEA CIRRIGERA) FROM SHORT MOUNTAIN, TENNESSEE 1,2 1 MATTHEW L. NIEMILLER AND BRIAN T. MILLER 1Department of Biology, Middle Tennessee State University, Murfreesboro, Tennessee 37132, USA 2Corresponding author/Present Address: Department of Ecology and Evolutionary Biology, University of Tennessee, Knoxville, Tennessee 37996, USA, e-mail: [email protected] Abstract.—The Southern Two-lined Salamander, Eurycea cirrigera, typically inhabits the margins of small, rocky streams, springs, and seeps in forested areas. The species is found only occasionally in subterranean habitats and, consequently, is considered a cave visitor (accidental or trogloxene). However, we discovered egg clutches in the deep cave zone of a subterranean stream during January and February 2005, indicating that some individuals are adapted to reproduce in caves. Eggs were attached singly to form monolayer masses on the undersurfaces of submerged rocks; females were found attending three of nine clutches. We determined the total number of eggs/clutch, mass surface area, egg and embryo size, and stage of development using digital images of each clutch. Embryo length correlated positively with developmental stage. Duration of embryonic period ranged from 35-42 days; consequently, eggs were laid from early to mid-January and larvae hatched from late February to early March. Adult males and females migrated into the cave to breed during late autumn. Males exited the cave after mating; whereas, females brooded their eggs and exited the cave only after eggs hatched. Larvae drifted downstream and out of the cave following heavy winter and early spring rains. -
Successful Reproduction of the Mole Salamander Ambystoma Talpoideum in Captivity, with an Emphasis on Stimuli Environmental Determinants
SHORT NOTE The Herpetological Bulletin 141, 2017: 28-31 Successful reproduction of the mole salamander Ambystoma talpoideum in captivity, with an emphasis on stimuli environmental determinants AXEL HERNANDEZ Department of Environmental Sciences, Faculty of Sciences and Technics, University Pasquale Paoli of Corsica, Corte, 20250, France Author Email: [email protected] ABSTRACT - Generating and promoting evidence-based husbandry protocols for urodeles, commonly known as newts and salamanders, is urgently needed because most of the up-to-date ex situ programs are focused on frogs and toads than Urodela. Data on biology, life history, ecology and environmental parameters are lacking for many species and are needed to establish suitable husbandry and breeding conditions in captive environments. Two adult females and two adult males, of the mole salamander Ambystoma talpoideum successfully reproduced in captivity. It was found that reproduction of this species depends on various complex stimuli: including natural photoperiod 12:12, rainwater (acidic to neutral pH) and an aquarium full of various debris. Additionally high temperature variations ranging from 2 °C to 17 °C (a decrease followed by an increase) between November and February showed that it is possible to breed adults in aquariums provided the right stimuli are applied at the right moment of time in winter. A. talpoideum shows an explosive breeding mode as previously reported for the whole genus Ambystoma. INTRODUCTION with an emphasis on the environmental determinant stimuli involved. These data may assist in improving breeding these ince the 1980s, the current global amphibian extinction salamanders under artificial conditions. crisis has been discussed and acknowledged (Wake, A.