Vernacular Name AMPHIUMA, ONE-TOED (Aka: Congo Eel, Congo Snake, Ditch Eel, Fish Eel and Lamprey Eel)

Total Page:16

File Type:pdf, Size:1020Kb

Vernacular Name AMPHIUMA, ONE-TOED (Aka: Congo Eel, Congo Snake, Ditch Eel, Fish Eel and Lamprey Eel) 1/6 Vernacular Name AMPHIUMA, ONE-TOED (aka: Congo Eel, Congo Snake, Ditch Eel, Fish Eel and Lamprey Eel) GEOGRAPHIC RANGE Eastern Gulf coast. HABITAT Wetlands: slow moving or stagnant freshwater rivers/streams/creeks and bogs, marshes, swamps, fens and peat lands. CONSERVATION STATUS IUCN: Near Threatened (2016). Population Trend: Decreasing. Because of the limited extent of its occurrence and because of the declining extent and quality of its habitat, this species is close to qualifying for Vulnerable. COOL FACTS Amphiumas are commonly known as "Congo eels," a misnomer. First of all, amphiumas are amphibians, rather than fish (which eels are). This notwithstanding, amphiumas bear resemblance to the elongate fishes. It is easy to overlook the diminutive legs, and the lack of any external gills adds to the similarity between the amphiumas and eels. Amphiumas are adapted for digging and tunneling. They seem to spend most of the time in muddy burrows and are rarely observed in the wild. They never fully metamorphose and retain larval characteristics in varying degrees into adulthood: one pair of the larval gill slits is retained and never disappears, no eyelids, no tongue and the presence of 4 gill arches with a single respiratory opening between the 3 rd--4th arches. Amphiumas have two pairs of limbs, and the three species, all of which occur in the S.E. U.S, differ in regard to the number of toes at the ends of these limbs: one, two or three. These amphiumas possess tiny, single-toed limbs, one pair just behind the small gill opening at each side of the neck and another pair just ahead of the longitudinal anal slit . Because of its small size relative to other amphiumas and reduced number of toes, the one- Amphiuma, One-toed 2/6 toed amphiuma is considered a dwarf species Despite an aquatic lifestyle, they breathe air through their lungs by periodically poking the nostrils above the surface of the water. They can exist up to 3 years without food. Amphiuma cells, especially the red blood cells, are the largest known in vertebrates and have long been used in physiological studies and in the classroom. Its fossil history dates back 65 million years, almost to the time of the disappearance of the dinosaurs. DIET In wild: aquatic, mud-dwelling invertebrates, presumably small clams, earthworms, larval aquatic insects, small beetles, worms, crustaceans, crayfish, amphibian larvae and snails. In zoo: Notably lacking from the diet are dragonfly naiads, salamander larvae, frog tadpoles, and small fish that co-habit the same mucky sites . MEDIAN LIFE EXPECTANCY Unknown. ENEMIES - DEFENSE Enemies: turtles (common snapping, mud, musk), snakes (mud, red-bellied water, brown water, queen, ring-necked, and cottonmouths), frogs (southern leopard, bronze), 2-toed amphiumas, feral pigs, raccoons, large wading birds and humans. Defense: a noxious skin secretion, producing foam, which is bitter tasting and slightly numbing. MATING - CARE OF THE YOUNG Courtship and reproductive process: Not yet recorded. Adult males may fight during the reproductive season. Nest: the female builds a nest in a moist place under logs, leaves or other cover. Fertilization: internal through the direct transfer of the spermatophore from the male’s cloaca into the female’s cloaca. Gestation: up to 6 months. Egg laying: probably occurs in the summer (June, July). Clutch size: Usually 50-200 eggs laid in rosary-like strings with a constriction between each egg. Hatching: occurs late summer/early fall. Hatchlings: 2” long. May have thin, feathery gills and a short larval life for a few days before metamorphosing into air-breathing juveniles. Parental Care: females care for the eggs by coiling around the egg mass. Sexual Maturity: at about 1 year. Mating Frequency: females reproduce biennially; males reproduce annually. SOCIAL INTERACTION Out of the water, they may emit a whistling sound. Amphiuma, One-toed 3/6 LIFE STYLE Activity Period: nocturnal, retreating into burrows during the day. Feeding Habits: - they lie in wait for passing prey or prowl in search of prey . - strong teeth and a powerful bite assist in subduing prey. Locomotion: lateral undulations. Aquatic. - However, they are capable, though rare, of exiting the water and traveling short distances on land, especially on wet nights or when females are brooding eggs. - Although they tend to keep to the thick bottom-layer of muck, which is anaerobic, one- toed amphiumas must come to the surface to breathe. During dry periods and droughts, to avoid desiccation, they will burrow into the moist mud, at least 12” underground (have been found at 3’ depths), where they can reside until the next rain. They are adapted for digging and tunneling. Seasonal migrations: in winter they have occasionally been found under large logs buried along stream courses in first-order stream valleys where the species is not found in the spring, summer or fall, presumably to find protection from cold weather in warmer headwater seepages. PHYSICAL General Description: an elongate, cylindrical, eel-like salamander. - Body: Cylindrical and highly elongated. Diameter: Slightly more than the width of a pencil. - Lacks costal grooves (unlike the other 2 amphiumids). - Gills: No external gills in adults. Single gill slit on each side of the neck in pharyngeal region. Size: 8.5”-12.5” long. No sexual dimorphism in body size. Considerably smaller than the other 2 amphiuma species. Body Covering: skin is smooth and slippery. Exudes slippery mucus. Is shed periodically and may be eaten, thus helping to sustain the species. Color: dark reddish brown or gray to grayish brown; the belly is only slightly lighter than the top side. Head: flat, pointed. Conical, cylindrical. - Snout: rounded, not depressed. Sensory Organs. - Eyes: very small. Eyelids absent. Dentition: distinct crowns. Strong. Their bite can be painful. Limbs: highly reduced. 4 extremely tiny limbs (0.4”-0.7”) relative to the body size; almost vestigial. Each limb has 1 toe. Not of use in locomotion. Amphiuma, One-toed 4/6 Tail: laterally compressed. About 22%-25% of the total length. Lungs: present. Breathe air through their lungs by periodically poking the nostrils above the surface of the water. Lungs begin to work after about 4 months when the external gills disappear. Can also breathe through the pharynx and the skin. TAXONOMY Phylum / Subphylum Chordata / Vertebrata Class / Subclass Amphibia / Lisamphibia Order / Suborder Caudata (Urodela) / Salamandroidea Family Amphiumidae Genus / Species Amphiuma pholeter It is thought that the generic name comes from the Greek words “ amphi” (on both sides) and “pneuma” (breath). This may refer to the permanent gill openings on both sides of the body. REFERENCES - Banks, R. C., R. W. MacDiarmid, A. L. Gardner, and W. C. Starnes 2003. Checklist of Vertebrates of the United States, the U.S. Territories, and Canada. - Frost, Darrel R. 1997. Amphibian Species of the World, A Taxonomic and Geographic Reference. Second edition. New York, New York, U.S.A. - Hammerson, Geoffrey, Dale Jackson 2004. Amphiuma pholeter. In: IUCN 2012. IUCN Red List of Threatened Species. Version 2012.1. www.iucnredlist.org - Hutchins, Michael, William E. Duellman and Neil Schlager, Editors. 2004. Grzimek’s Animal Life Encyclopedia. Vol. 6: Amphibians. Farmington Hills, MI. Gale Group. - Lannoo, Michael, ed: Amphibian Declines: The Conservation Status of United States Species , 2005. The Regents of the University of California), used with permission of University of California Press. - Means, D. Bruce. 2004. One-toed Amphiuma, Amphiuma pholeter Neill. In Ralph E. Mirarchi, ed. Vertebrate and Selected Invertebrate Wildlife of Alabama. - Mount, Robert H. 1975. The Reptiles and Amphibians of Alabama . The University of Alabama Press: Tuscaloosa, Alabama. - AmphibiaWeb: 2007. Berkeley, California: Amphibia Web. http://amphibiaweb.org/. - Frost, Darrell and The American Museum of Natural History. research.amnh.org/herpetology/amphibia/references.php?id=25257;1998-2007 - Georgia Museum of Natural History and Georgia Department of Natural Resources 1 June 2000; museum.nhm.uga.edu/gawildlife/amphibians/caudata/amphiumidae/apholeter.html - Larson, Allan. 1996. Amphiumidae. Amphiumas. Version 01 January 1996 (under construction). http://tolweb.org/Amphiumidae/15440/1996.01.01 in The Tree of Life Web Project, http://tolweb.org/ - Means, Bruce D. www.outdooralabama.com/watchable-wildlife/what/Amphibians/Salamanders/ota.cfm Amphiuma, One-toed 5/6 - Myers, P., R. Espinosa, C. S. Parr, T. Jones, G. S. Hammond, and T. A. Dewey. 2006. The Animal Diversity Web (online). http://animaldiversity.org. - National Zoo Fact Sheet: http://natzoo.si.edu/Animals/ReptilesAmphibians/Facts/FactSheets/Threetoedamphiuma.cfm - NatureServe. 2006. NatureServe Explorer: An online encyclopedia of life [web application]. Version 6.1. NatureServe, Arlington, Virginia. http://www.natureserve.org/explorer. - Salamanders of Georgia and South Carolina. Photos by J.D. Willson. www.uga.edu/srelherp/salamanders/amppho.htm - www.caudata.org/cc/species/Amphiuma/Amphiuma.shtml - The IUCN Red List of Threatened Species. Version 2016-1. <www.iucnredlist.org>. Downloaded on 02 July 2016. Prepared by: Judith Ehrman, docent Date: 04-01-07 Photo by: Lyn Tunmer, PZ Graphics Map by: Judy Ehrman – Bob Sloane, docents Approved by: Date: Reformatted by: Judith Ehrman and Bob Sloane, docents Date: 06-19-12 Amphiuma, One-toed 6/6 This page intentionally left blank .
Recommended publications
  • 2020 Mississippi Bird EA
    ENVIRONMENTAL ASSESSMENT Managing Damage and Threats of Damage Caused by Birds in the State of Mississippi Prepared by United States Department of Agriculture Animal and Plant Health Inspection Service Wildlife Services In Cooperation with: The Tennessee Valley Authority January 2020 i EXECUTIVE SUMMARY Wildlife is an important public resource that can provide economic, recreational, emotional, and esthetic benefits to many people. However, wildlife can cause damage to agricultural resources, natural resources, property, and threaten human safety. When people experience damage caused by wildlife or when wildlife threatens to cause damage, people may seek assistance from other entities. The United States Department of Agriculture, Animal and Plant Health Inspection Service, Wildlife Services (WS) program is the lead federal agency responsible for managing conflicts between people and wildlife. Therefore, people experiencing damage or threats of damage associated with wildlife could seek assistance from WS. In Mississippi, WS has and continues to receive requests for assistance to reduce and prevent damage associated with several bird species. The National Environmental Policy Act (NEPA) requires federal agencies to incorporate environmental planning into federal agency actions and decision-making processes. Therefore, if WS provided assistance by conducting activities to manage damage caused by bird species, those activities would be a federal action requiring compliance with the NEPA. The NEPA requires federal agencies to have available
    [Show full text]
  • Chassahowitzka Chassahowitzka Plan Comprehensive Conservation
    U.S. Fish & Wildlife Service Chassahowitzka NationalWildlifeRefuge Chassahowitzka National Wildlife Refuge Refuge Manager: Michael Lusk, (Project Leader) 1502 S.E. Kings Bay Drive Crystal River, FL 34429 Phone: (352) 563-2088 / ext. 202 Fax: (352) 795-7961 E-mail: [email protected] U.S. Fish & Wildlife Service 1 800/344 WILD http://www.fws.gov Chassahowitzka National Wildlife Refuge Comprehensive ConservationPlan September 2012 Comprehensive Conservation Plan USFWS Photos Photo Credits: Operation Migration, by Keith Ramos Dog Island, by Amber Breland Chass Aerial, by Joyce Kleen Comprehensive Conservation Plans provide long-term guidance for manage- ment decisions; set forth goals, objectives, and strategies needed to accom- plish refuge purposes; and identify the Fish and Wildlife Service’s best esti- mate of future needs. These plans detail program planning levels that are sometimes substantially above current budget allocations and, as such, are primarily for Service strategic planning and program prioritization purposes. The plans do not constitute a commitment for staffing increases, operational and maintenance increases, or funding for future land acquisition. Chassahowitzka National Wildlife Refuge Comprehensive Conservation Plan U.S. Department of the Interior Fish and Wildlife Service Southeast Region September 2012 COMPREHENSIVE CONSERVATION PLAN CHASSAHOWITZKA NATIONAL WILDLIFE REFUGE Citrus and Hernando Counties, Florida U.S. Department of the Interior Fish and Wildlife Service Southeast Region Atlanta, Georgia September
    [Show full text]
  • AMPHIBIANS of OHIO F I E L D G U I D E DIVISION of WILDLIFE INTRODUCTION
    AMPHIBIANS OF OHIO f i e l d g u i d e DIVISION OF WILDLIFE INTRODUCTION Amphibians are typically shy, secre- Unlike reptiles, their skin is not scaly. Amphibian eggs must remain moist if tive animals. While a few amphibians Nor do they have claws on their toes. they are to hatch. The eggs do not have are relatively large, most are small, deli- Most amphibians prefer to come out at shells but rather are covered with a jelly- cately attractive, and brightly colored. night. like substance. Amphibians lay eggs sin- That some of these more vulnerable spe- gly, in masses, or in strings in the water The young undergo what is known cies survive at all is cause for wonder. or in some other moist place. as metamorphosis. They pass through Nearly 200 million years ago, amphib- a larval, usually aquatic, stage before As with all Ohio wildlife, the only ians were the first creatures to emerge drastically changing form and becoming real threat to their continued existence from the seas to begin life on land. The adults. is habitat degradation and destruction. term amphibian comes from the Greek Only by conserving suitable habitat to- Ohio is fortunate in having many spe- amphi, which means dual, and bios, day will we enable future generations to cies of amphibians. Although generally meaning life. While it is true that many study and enjoy Ohio’s amphibians. inconspicuous most of the year, during amphibians live a double life — spend- the breeding season, especially follow- ing part of their lives in water and the ing a warm, early spring rain, amphib- rest on land — some never go into the ians appear in great numbers seemingly water and others never leave it.
    [Show full text]
  • Aquatic Feeding in Salamanders
    CHAPTER 3 Aquatic Feeding in Salamanders STEPHEN M. DEBAN AND DAVID B. WAKE Museum of Vertebrate Zoology and Department oflntegrative Biology University of California Berkeley, California 94720 I. INTRODUCTION canum. Some undergo partial metamorphosis and pos- A. Systematics sess both adult and larval features when reproductive, B. Natural History such as the fully aquatic Cryptobranchus. Others are C. Feeding Modes and Terminology primarily terrestrial and become secondarily aquatic 11. MORPHOLOGY as metamorphosed adults, notably during the breed- A. Larval Morphology ing season. The family Salamandridae contains the B. Adult Morphology most representatives of this type, known commonly C. Sensory and Motor Systems as newts. 111. FUNCTION A. Ingestion Behavior and Kinematics Salamanders covered in this chapter may be terres- B. Prey Processing trial, semiaquatic, or fully aquatic. They may return to C. Functional Morphology the water only periodically and may feed on both land D. Biomechanics and in water. Discussion here focuses on the aquatic E. Metamorphosis feeding biology of these taxa. Terrestrial feeding of F. Performance semiaquatic and terrestrial salamanders is discussed G. Variation in the next chapter. Here we describe the various feed- IV. DIVERSITY AND EVOLUTION ing behaviors: foraging, ingestion (prey capture), prey A. Features of Salamander Families processing, intraoral prey transport, and swallowing. B. Phylogenetic Patterns of Feeding Form and Function We review the relevant morphology and function of V. OPPORTUNITIES FOR FUTURE RESEARCH the sensory and motor systems and analyze the bio- References mechanical function of the feeding apparatus. Finally, we consider the evolution of aquatic feeding systems within and among the major taxa of salamanders.
    [Show full text]
  • TRAPPING SUCCESS and POPULATION ANALYSIS of Siren Lacertina and Amphiuma Means
    TRAPPING SUCCESS AND POPULATION ANALYSIS OF Siren lacertina AND Amphiuma means By KRISTINA SORENSEN A THESIS PRESENTED TO THE GRADUATE SCHOOL OF THE UNIVERSITY OF FLORIDA IN PARTIAL FULFILLMENT OF THE REQUIREMENTS FOR THE DEGREE OF MASTER OF SCIENCE UNIVERSITY OF FLORIDA 2003 ACKNOWLEDGMENTS I thank my committee members Lora Smith, Franklin Percival, and Dick Franz for all their support and advice. The Department of Interior's Student Career Experience Program and the U.S. Geological Survey's Amphibian Research and Monitoring Initiative provided funding for this project. I thank those involved with these programs who have helped me over the last three years: David Trauger, Ken Dodd, Jamie Barichivich, Jennifer Staiger, Kevin Smith, and Steve Johnson. Numerous people helped with field work: Audrey Owens, Maya Zacharow, Chris Gregory, Matt Chopp, Amanda Rice, Paul Loud, Travis Tuten, Steve Johnson, and Jennifer Staiger, Lora Smith, and the UF Wildlife Field Techniques Courses of2001-2002. Paul Moler and John Jensen provided advice and shared their wealth of herpetological knowledge. I thank the staff of Okefenokee National Wildlife Refuge and Steve Coates, manager of the Ordway Preserve, for their assistance on numerous occasions and for permission to conduct research on their property. Marinela Capanu of the IFAS Statistical Consulting Unit assisted with statistical analysis. Julien Martin, Bob Dorazio, Rob Bennets, and Cathy Langtimm provided advice on population analysis. I also thank the administrative staff of the Florida Caribbean Science Center and the Florida Cooperative Fish and Wildlife Research Unit. I am much indebted to all of these people, without whom this thesis would not have been possible.
    [Show full text]
  • Tall Timbers Bibliography
    Tall Timbers Bibliography Article Citations by Tall Timbers Authors Include the Following Areas of Interest Fire Research Quail Research Conservation Wildlife Management Outreach Geospatial Techniques & Tools Forest Management This Bibliography includes almost 1,400 articles published by Tall Timbers Staff and Associates, since 1958. It is a searchable PDF file. In Adobe Acrobat, it can be searched by author, date or subject matter. From the Edit menu, chose Find (Ctrl+F ) or Advanced Search (Shift+Ctrl+F). Bibliography 1. Engstrom, R.T. and G. Mikusinski. 1998. Ecological neighborhoods in red-cockaded woodpecker populations. The Auk. Vol. 115(2):473-478. 2. Abele, L.G. and D.B. Means. 1977. Sesarma jarvisi and Sesarma cookei: montane, terrestrial grapsid crabs in Jamaica (Decapoda). Crustaceana. Vol. 32(1):91-93. 3. Larson, B.C., W.K. Moser, and V.K. Mishra. 1998. Some relationships between silvicultural treatments and symmetry of stem growth in a red pine stand. Northern Journal of Applied Forestry. Vol. 15(2):90-93. 4. Altieri, M.A. 1981. Effect of time of disturbance on the dynamics of weed communities in north Florida. Geobios. Vol. 8(4):145-151. 5. Altieri, M.A. and J.D. Doll. 1978. The potential of allelopathy as a tool for weed management in crop fields. Pans. Vol. 24(4):495-502. 6. Loughry, W.J. and C.M. McDonough. 1998. Spatial patterns in a population of nine-banded armadillos (Dasy pus novemcinctus). The American Midland Naturalist. Vol. 140(1):161-169. 7. McNair, D.B. and J.A. Gore. 1998. Occurrences of flamingos in northwest Florida, including a recent record of the greater flamingo (Phoenicopterus ruber).
    [Show full text]
  • The Salamanders of Tennessee
    Salamanders of Tennessee: modified from Lisa Powers tnwildlife.org Follow links to Nongame The Salamanders of Tennessee Photo by John White Salamanders are the group of tailed, vertebrate animals that along with frogs and caecilians make up the class Amphibia. Salamanders are ectothermic (cold-blooded), have smooth glandular skin, lack claws and must have a moist environment in which to live. 1 Amphibian Declines Worldwide, over 200 amphibian species have experienced recent population declines. Scientists have reports of 32 species First discovered in 1967, the golden extinctions, toad, Bufo periglenes, was last seen mainly species of in 1987. frogs. Much attention has been given to the Anurans (frogs) in recent years, however salamander populations have been poorly monitored. Photo by Henk Wallays Fire Salamander - Salamandra salamandra terrestris 2 Why The Concern For Salamanders in Tennessee? Their key role and high densities in many forests The stability in their counts and populations Their vulnerability to air and water pollution Their sensitivity as a measure of change The threatened and endangered status of several species Their inherent beauty and appeal as a creature to study and conserve. *Possible Factors Influencing Declines Around the World Climate Change Habitat Modification Habitat Fragmentation Introduced Species UV-B Radiation Chemical Contaminants Disease Trade in Amphibians as Pets *Often declines are caused by a combination of factors and do not have a single cause. Major Causes for Declines in Tennessee Habitat Modification -The destruction of natural habitats is undoubtedly the biggest threat facing amphibians in Tennessee. Housing, shopping center, industrial and highway construction are all increasing throughout the state and consequently decreasing the amount of available habitat for amphibians.
    [Show full text]
  • I Online Supplementary Data – Sexual Size Dimorphism in Salamanders
    Online Supplementary data – Sexual size dimorphism in salamanders Supplementary data S1. Species data used in this study and references list. Males Females SSD Significant test Ref Species n SVL±SD n SVL±SD Andrias davidianus 2 532.5 8 383.0 -0.280 12 Cryptobranchus alleganiensis 53 277.4±5.2 52 300.9±3.4 0.084 Yes 61 Batrachuperus karlschmidti 10 80.0 10 84.8 0.060 26 Batrachuperus londongensis 20 98.6 10 96.7 -0.019 12 Batrachuperus pinchonii 5 69.6 5 74.6 0.070 26 Batrachuperus taibaiensis 11 92.9±12.1 9 102.1±7.1 0.099 Yes 27 Batrachuperus tibetanus 10 94.5 10 92.8 -0.017 12 Batrachuperus yenyuadensis 10 82.8 10 74.8 -0.096 26 Hynobius abei 24 57.8±2.1 34 55.0±1.2 -0.048 Yes 92 Hynobius amakusaensis 22 75.4±4.8 12 76.5±3.6 0.014 No 93 Hynobius arisanensis 72 54.3±4.8 40 55.2±4.8 0.016 No 94 Hynobius boulengeri 37 83.0±5.4 15 91.5±3.8 0.102 Yes 95 Hynobius formosanus 15 53.0±4.4 8 52.4±3.9 -0.011 No 94 Hynobius fuca 4 50.9±2.8 3 52.8±2.0 0.037 No 94 Hynobius glacialis 12 63.1±4.7 11 58.9±5.2 -0.066 No 94 Hynobius hidamontanus 39 47.7±1.0 15 51.3±1.2 0.075 Yes 96 Hynobius katoi 12 58.4±3.3 10 62.7±1.6 0.073 Yes 97 Hynobius kimurae 20 63.0±1.5 15 72.7±2.0 0.153 Yes 98 Hynobius leechii 70 61.6±4.5 18 66.5±5.9 0.079 Yes 99 Hynobius lichenatus 37 58.5±1.9 2 53.8 -0.080 100 Hynobius maoershanensis 4 86.1 2 80.1 -0.069 101 Hynobius naevius 72.1 76.7 0.063 102 Hynobius nebulosus 14 48.3±2.9 12 50.4±2.1 0.043 Yes 96 Hynobius osumiensis 9 68.4±3.1 15 70.2±3.0 0.026 No 103 Hynobius quelpaertensis 41 52.5±3.8 4 61.3±4.1 0.167 Yes 104 Hynobius
    [Show full text]
  • Amphiumidae Cryptobranchidae Proteidae
    Amphiumidae Amphiuma means – Two-toed Amphiuma cryptobranchidae Cryptobranchus alleganiensis – Hellbender Proteidae Necturus maculosus – Mudpuppy Sirenidae Siren intermedia – Lesser Siren Ambystomatidae Ambystoma gracile – Northwestern Salamander Ambystoma tigrinum – Tiger Salamander Ambystoma macrodactylum – Long-toed Salamander Ambystoma californiense – California Tiger Salamander Dicamptodontidae Dicamptodon ensatus – California Giant Salamander Dicamptodon tenebrosus – Pacific Giant Salamander Rhyacotritonidae Rhyacotriton variegatus – Southern Torrent Salamander Salamandridae Taricha torosa – California Newt Taricha Sierrae – Sierra Newt Taricha rivularis – Red-bellied Newt Taricha granulosa – Rough-skinned Newt Plethodontidae Aneides flavipunctatus – Black Salamander Aneides vagrans – Wandering Salamander Aneides ferreus – Clouded Salamander Aneides lugubris – Arboreal Salamander Plethodontidae Ensatina eschscholtzii – Ensatina Plethodontidae Batrachoseps attenuatus – California Slender Salamander Batrachoseps gavilanensis – Gabilan Mountains Slender Salamander Plethodontidae Plethodon dunni – Dunn’s Salamander Plethodon stormi – Siskiyou Mountains Salamander Plethodon elongatus – Del Norte Salamander Plethodon asupak – Scott Bar Salamander Plethodontidae Hydromantes brunus – Limestone Salamander Hydromantes platycephalus – Mount Lyell Salamander Hydromantes shastae – Shasta Salamander Ascaphidae Ascaphus truei – Tailed Frog Pelobatidae Spea hammondii – Western Spadefoot Spea intermontana – Great Basin Spadefoot Scaphiopus couchi
    [Show full text]
  • Key to the Identification of Streamside Salamanders
    Key to the Identification of Streamside Salamanders Ambystoma spp., mole salamanders (Family Ambystomatidae) Appearance : Medium to large stocky salamanders. Large round heads with bulging eyes . Larvae are also stocky and have elaborate gills. Size: 3-8” (Total length). Spotted salamander, Ambystoma maculatum Habitat: Burrowers that spend much of their life below ground in terrestrial habitats. Some species, (e.g. marbled salamander) may be found under logs or other debris in riparian areas. All species breed in fishless isolated ponds or wetlands. Range: Statewide. Other: Five species in Georgia. This group includes some of the largest and most dramatically patterned terrestrial species. Marbled salamander, Ambystoma opacum Amphiuma spp., amphiuma (Family Amphiumidae) Appearance: Gray to black, eel-like bodies with four greatly reduced, non-functional legs (A). Size: up to 46” (Total length) Habitat: Lakes, ponds, ditches and canals, one species is found in deep pockets of mud along the Apalachicola River floodplains. A Range: Southern half of the state. Other: One species, the two-toed amphiuma ( A. means ), shown on the right, is known to occur in A. pholeter southern Georgia; a second species, ,Two-toed amphiuma, Amphiuma means may occur in extreme southwest Georgia, but has yet to be confirmed. The two-toed amphiuma (shown in photo) has two diminutive toes on each of the front limbs. Cryptobranchus alleganiensis , hellbender (Family Cryptobranchidae) Appearance: Very large, wrinkled salamander with eyes positioned laterally (A). Brown-gray in color with darker splotches Size: 12-29” (Total length) A Habitat: Large, rocky, fast-flowing streams. Often found beneath large rocks in shallow rapids. Range: Extreme northern Georgia only.
    [Show full text]
  • Streamside Salamander Identification Guide
    Key to the Identification of Streamside Salamanders 1 Ambystoma spp., mole salamanders (Family Ambystomatidae) Appearance: Medium to large stocky salamanders. Large round heads with bulging eyes. Larvae are also stocky and have elaborate gills. Size: 3-8” (Total length). Spotted salamander, Ambystoma maculatum Habitat: Burrowers that spend much of their life below ground in terrestrial habitats. Some species, (e.g. marbled salamander) may be found under logs or other debris in riparian areas. All species breed in fishless isolated ponds or wetlands. Range: Statewide. Other: Five species in Georgia. This group includes some of the largest and most dramatically patterned terrestrial species. Marbled salamander, Ambystoma opacum Amphiuma spp., amphiuma (Family Amphiumidae) Appearance: Gray to black, eel-like bodies with four greatly reduced, non-functional legs (A). Size: up to 46” (Total length) Habitat: Lakes, ponds, ditches and canals, one species is found in deep pockets of mud along the Apalachicola River floodplains. A Range: Southern half of the state. A Other: One species, the two-toed amphiuma (A. means), shown on the right, is known to occur in A. pholeter southern Georgia; a second species, ,Two-toed amphiuma, Amphiuma means may occur in extreme southwest Georgia, but has yet to be confirmed. The two-toed amphiuma (shown in photo) has two diminutive toes on each of the front limbs. 2 Cryptobranchus alleganiensis, hellbender (Family Cryptobranchidae) Appearance: Very large, wrinkled salamander with eyes positioned laterally (A). Brown-gray in color with darker splotches Size: 12-29” (Total length) A Habitat: Large, rocky, fast-flowing streams. Often found beneath large rocks in shallow rapids.
    [Show full text]
  • (Amphibia, Urodela) from the Late Jurassic of Qinglong, Hebei Province, China
    RESEARCH ARTICLE A New Basal Salamandroid (Amphibia, Urodela) from the Late Jurassic of Qinglong, Hebei Province, China Jia Jia, Ke-Qin Gao* School of Earth and Space Sciences, Peking University, 5 Yiheyuan Road, Beijing, 100871, China * [email protected] a11111 Abstract A new salamandroid salamander, Qinglongtriton gangouensis (gen. et sp. nov.), is named and described based on 46 fossil specimens of juveniles and adults collected from the Upper Jurassic (Oxfordian) Tiaojishan Formation cropping out in Hebei Province, China. OPEN ACCESS The new salamander displays several ontogenetically and taxonomically significant fea- Citation: Jia J, Gao K-Q (2016) A New Basal tures, most prominently the presence of a toothed palatine, toothed coronoid, and a unique Salamandroid (Amphibia, Urodela) from the Late pattern of the hyobranchium in adults. Comparative study of the new salamander with previ- Jurassic of Qinglong, Hebei Province, China. PLoS ONE 11(5): e0153834. doi:10.1371/journal. ously known fossil and extant salamandroids sheds new light on the early evolution of the pone.0153834 Salamandroidea, the most species-diverse clade in the Urodela. Cladistic analysis places Editor: William Oki Wong, Institute of Botany, CHINA the new salamander as the sister taxon to Beiyanerpeton, and the two taxa together form the basalmost clade within the Salamandroidea. Along with recently reported Beiyanerpe- Received: December 11, 2015 ton from the same geological formation in the neighboring Liaoning Province, the discovery Accepted: April 2, 2016 of Qinglongtriton indicates that morphological disparity had been underway for the sala- Published: May 4, 2016 mandroid clade by early Late Jurassic (Oxfordian) time. Copyright: © 2016 Jia, Gao.
    [Show full text]