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Comparative Osteology and Evolution of the Lungless Salamanders, Family Plethodontidae David B
COMPARATIVE OSTEOLOGY AND EVOLUTION OF THE LUNGLESS SALAMANDERS, FAMILY PLETHODONTIDAE DAVID B. WAKE1 ABSTRACT: Lungless salamanders of the family Plethodontidae comprise the largest and most diverse group of tailed amphibians. An evolutionary morphological approach has been employed to elucidate evolutionary rela tionships, patterns and trends within the family. Comparative osteology has been emphasized and skeletons of all twenty-three genera and three-fourths of the one hundred eighty-three species have been studied. A detailed osteological analysis includes consideration of the evolution of each element as well as the functional unit of which it is a part. Functional and developmental aspects are stressed. A new classification is suggested, based on osteological and other char acters. The subfamily Desmognathinae includes the genera Desmognathus, Leurognathus, and Phaeognathus. Members of the subfamily Plethodontinae are placed in three tribes. The tribe Hemidactyliini includes the genera Gyri nophilus, Pseudotriton, Stereochilus, Eurycea, Typhlomolge, and Hemidac tylium. The genera Plethodon, Aneides, and Ensatina comprise the tribe Pleth odontini. The highly diversified tribe Bolitoglossini includes three super genera. The supergenera Hydromantes and Batrachoseps include the nominal genera only. The supergenus Bolitoglossa includes Bolitoglossa, Oedipina, Pseudoeurycea, Chiropterotriton, Parvimolge, Lineatriton, and Thorius. Manculus is considered to be congeneric with Eurycea, and Magnadig ita is congeneric with Bolitoglossa. Two species are assigned to Typhlomolge, which is recognized as a genus distinct from Eurycea. No. new information is available concerning Haptoglossa. Recognition of a family Desmognathidae is rejected. All genera are defined and suprageneric groupings are defined and char acterized. Range maps are presented for all genera. Relationships of all genera are discussed. -
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. -
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 -
AMPHIBIA: CAUDATA: PROTEIDAE Catalogue of American Amphibians and Reptiles
m AMPHIBIA: CAUDATA: PROTEIDAE Catalogue of American Amphibians and Reptiles. Dundee, H.A. 1998. Nectlrrlrsprmctntus. Necturr~spunctatus (Gibbes) Dwarf Waterdog Nectlrr~rs: Baird 1850:25 1 . Indicated Necturus -Gibbes. not yet published. Metzohrnnchus punctatris Gibbes 1850: 159. Type locality, "South Santee River, a few miles from its mouth." Holotype, presumably National Museum of Natural History (USNM) 11813 (not seen by author). The first actual specimen was collected in February 1848, by one of Mr. Augustus Shool- bred's negro workers on Shoolbred's plantation but was lost. A few weeks later, additional specimens were presented to Gibbes by Dr. A. Gadsden, and again, shortly thereafter, ad- ditional specimens were given to Gibbes by Mr. Shoolbred. All apparently came from Shoolbred's plantation in 1848. MAP. Range of Necturrrspunctarus. The circle marks the type locality Two others, given to Gibbes by Shoolbred in March 1850, and dots represent most known localities. apparently came from his father's (Dr. Shoolbred) plantation; all were exhibited in Charleston, South Carolina in March 1850 (see Comment). Cope ( 1889) stated that USNM 11 8 13 mander and the smallest species of the genus, maximum TL was the type; it was received from Gibbes and. according to being 189 mm. The tail length ranges from about 3&41% (av- Cope (1 889), was collected in 1850. Cope's mention of cloa- erage 38%) of the TL in adults, with sexual maturity being cal papillae in USNM 11813 would indicate that the speci- reached at approximately 65-70 mm SVL (about 4.5 or more men was a male. -
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. -
Sexual Dimorphism in the Three-Toed Amphiuma, Amphiuma Tridactylum: Sexual Selection Or Ecological Causes?
Copeia 2008, No. 1, 39–42 Sexual Dimorphism in the Three-toed Amphiuma, Amphiuma tridactylum: Sexual Selection or Ecological Causes? Clifford L. Fontenot, Jr.1 and Richard A. Seigel2 Sexual dimorphism is widespread among vertebrates, and may be attributable to sexual selection, differences in ecology between the sexes, or both. The large aquatic salamander, Amphiuma tridactylum, has been suggested to have male biased sexual dimorphism that is attributable to male–male combat, although detailed evidence is lacking. To test this, data were collected on A. tridactylum head and body size, as well as on bite-marks inflicted by conspecifics. Amphiuma tridactylum is sexually dimorphic in several characters. There was no sex difference in body length, but males had heavier bodies than females of the same body length. Larger males had wider and longer heads than larger females, but whether any of these sexually dimorphic characters are attributable to differences in diet is unknown because diet data (by sex) are lacking. There was no difference in the number of bite-marks between males and females, and juveniles also possessed bite-marks, suggesting that the biting is not necessarily related to courtship or other reproductive activities. In addition, fresh bite-marks were present on individuals during months well outside of the breeding season. Biting was observed in the field and lab to occur by both sexes on both sexes, during feeding-frenzy type foraging. Thus, biting is likely related to foraging rather than to courtship. The sexually dimorphic characters remain unexplained, pending sex-specific diet data, but there is no evidence that they are related to male–male combat or to courtship. -
Volume 2, Chapter 14-8: Salamander Mossy Habitats
Glime, J. M. and Boelema, W. J. 2017. Salamander Mossy Habitats. Chapt. 14-8. In: Glime, J. M. Bryophyte Ecology. Volume 2. 14-8-1 Bryological Interaction.Ebook sponsored by Michigan Technological University and the International Association of Bryologists. Last updated 19 July 2020 and available at <http://digitalcommons.mtu.edu/bryophyte-ecology2/>. CHAPTER 14-8 SALAMANDER MOSSY HABITATS Janice M. Glime and William J. Boelema TABLE OF CONTENTS Tropical Mossy Habitats – Plethodontidae........................................................................................................ 14-8-3 Terrestrial and Arboreal Adaptations ......................................................................................................... 14-8-3 Bolitoglossa (Tropical Climbing Salamanders) ......................................................................................... 14-8-4 Bolitoglossa diaphora ................................................................................................................................ 14-8-5 Bolitoglossa diminuta (Quebrada Valverde Salamander) .......................................................................... 14-8-5 Bolitoglossa hartwegi (Hartweg's Mushroomtongue Salamander) ............................................................ 14-8-5 Bolitoglossa helmrichi ............................................................................................................................... 14-8-5 Bolitoglossa jugivagans ............................................................................................................................ -
Tennessee Salamander Identification
1/24/2010 Salamanders of Tennessee Matthew L. Niemiller 21 January 2010 Salamander Anatomy Costal groove Mental gland Cirri Cornified toe pads Nasolabial groove Hellbender Cryptobranchus alleganiensis • Family Cryptobranchidae – Up to 740 mm TL – Lack external gills; gills covered by skin – Flattened heads with small eyes – Conspicuously wrinkled skin along sides to aid in cutaneous respiration – Long oar‐like tails and short robust legs – External fertilization 1 1/24/2010 Mudpuppy Necturus maculosus • Family Proteidae – Up to 40 mm TL – Neotenic; external gills throughout life – Four toes on each foot – Also possess lungs – Long oar‐like tails and short robust legs – Primarily found in rivers in Tennessee Family Ambystomatidae • Large, robust salamanders with short but large, rounded heads • Conspicuous costal grooves present • Nasolabial grooves absent • Possess lungs • Larvae are robust with well‐developed caudal fins and large heads • Six species in Tennessee • Inhabit a variety of habitats but are most common in forests in close proximity to breeding sites, such as ephemeral ponds and flooded meadows • Throughout the majority of the year, adults reside underground in burrows but come to the surface during the breeding season Spotted Salamander Ambystoma maculatum • Up to 248 mm TL • Black to gray ground color with conspicuous yellow to orange paired spots on the dorsum • Males with swollen vents during breeding season • 12 costal grooves • Breeding January ‐ April 2 1/24/2010 Marbled Salamander Ambystoma opacum • Smaller, up to -
Contents & Distribution Data
3 Contents & distribution data Introduction/Einführung ^ 7 Howtousethisbook/Benutzerhinweise 17 References/Literaturverzeichnis 18 Acknowledgments/Danksagung 20 CAUDATA FISCHER VON WALDHEIM, 1813 - Tailed amphibians (newts & salamanders)/Schwanzlurche (Molche & Salamander) HYNOBIIDAE COPE, 1859 - Asiatic salamanders/Asiatische Salamander Salamandrella DYBOWSKI, 1870 - Siberian salamanders/Sibirische Salamander Salamandrella keyserlingii DYBOWSKI, 1870 - Siberian Salamander/Sibirischer Salamander 21 Eastern European Russia (east across Siberia, northern Mongolia, northeaslern China, northern and northwestern North Korea and Hokkaido Island, Japan) PLETHODONTIDAE GRAY, 1850 - Lungless salamanders/Lungenlose Salamander Atylod.es GISTEL, 1868 - Web-toed salamander/Höhlensalamander Atylodes genei (TEMMINCK & SCHLEGEL, 1838) - Sardinian cave Salamander/Sardischer Höhlensalamander 22 Italy (southwestern Sardinia) Speleomantes DUBOIS, 1984 - Web-toed salamanders/Höhlensalamander Speleomantes ambrosii (LANZA, 1954) - Ambrosi's cave Salamander/Ambrosis Höhlensalamander Speleomantes ambrosii ambrosii (LANZA, 1954) - French cave salamander/Französischer Höhlensalamander 24 Extreme southeastern France and extreme northwestern Italy Speleomantes ambrosii bianchii LANZA, CIMMARUTA, FORTI, BULLINI & NASCETTI, 2005 - Apuan Alps cave Salamander/Apuanischer Höhlensalamander 25 Northwestern Italy (Apuan Alps, Tuscany) Speleomantes flavus (STEFANI, 1969) - Monte Albo cave salamander/Monte Albo-Höhlensalamander 26 Italy (northeastern Sardinia) Speleomantes -
Lecture Roadmap General Characteristics
1/24/2013 WFS 433/533 1/24/2013 Lecture roadmap General Characteristics of Caudates Caudate Evolution Caudate Ecology Major Caudate families General Characteristics Very similar body plan - Small head, elongate body, four limbs, and tail Do not hop; use lateral undulation Do not actively vocalize Attract mates via pheromones (mental gland) Elaborate mating rituals (tail straddling) 1 1/24/2013 Caudate Phylogeny More Derived Less Derived Salamander Evolution Important themes in salamander evolution…. - Lunglessness - Small body size - Feeding strategies Convergent evolution; exploitation of different habitats - Tree-tops; prehensile tails (Bolitoglossines) - Longer bodies; reduced limb length - Webbed feet Salamander Evolution Body size variation (miniaturization) Hydromantes supramontis - Terrestrial species (Plethodontids) Lunglessness - General characteristic of terrestrial species Feeding strategies - Hyoid structure evolution - Evolved numerous times independently 2 1/24/2013 Caudate Distribution 10 families (9 depending on source) Low diversity throughout new-world tropics; absent entirely from old-world tropics Biology and ecology poorly understood Mostly Temperate Distribution Adaptive radiations 10 Families General Ecology Inhabit moist environments - Facilitate oxygen exchange Four families fully aquatic - Cryptobranchidae - Amphiumidae - Sirenidae - Proteidae Necturus maculosus Six families terrestrial (not fully) - Plethodontidae - Hynobiidae - Ambystomatidae - Dicamptodontidae (Maybe) - Rhyacotritonidae -
Caudata Density
CAUDATA DENSITY - What typical population density could you expect for the species in a hectare of ideal habitat? Species Common Name Density Cryptobranchidae Giant Salamander Cryptobranchus a. alleganiensis Eastern Hellbender 1-6 / 100m2 of stream in 4 populations in AR and MO (Peterson et al. 1988). N. fork of White River in MO has estimated 428 mature ind./km of stream (Nickerson and Mays 1973). 10 / 80-100m2 in optimal riffle habitats (Petranka 1998). Sirenidae Sirens Siren i. intermedia Eastern Lesser Siren 1.1 S. i. nettingi /m2 in TX (Gehlbach and Kennedy 1978) Siren lacertina Greater Siren Unk Amphiumidae Congo Eels Amphiuma means Two-toed Amphiuma Unk Proteidae Waterdogs Necturus m. maculosus Common Mudpuppy 382 / 700m of river in OH (Matson 1988) Necturus punctatus Dwarf Waterdog Unk Salamandridae True Salamanders Notophthalmus v. viridescens Red-spotted Newt 0.2 - 0.26 adults / sq m (Burton 1977), 0.16 - 2.5 adults / sq m (Morin 1983), 1adult / sq m (Bellis 1968), 0.03 efts / sq m of forest floor (Healy 1975) Ambystomatidae Mole Salamanders Ambystoma barbouri Streamside Salamander Unk Ambystoma jeffersonianum Jefferson Salamander Unk Ambystoma laterale Blue-spotted Salamander 15 and 12 hatchlings/m2 in two study pops in MI, up to 158 hatchlings/m2 in pools (Van Buskirk and Smith 1991) Ambystoma mabeei Mabee's Salamander Unk Ambystoma maculatum Spotted Salamander Unk Ambystoma opacum Marbled Salamander Unk Ambystoma talpoideum Mole Salamander Unk Ambystoma texanum Small-mouthed Salamander Unk Ambystoma t. tigrinum Eastern Tiger Salamander Unk Plethodontidae Lungless Salamanders Aneides aeneus Green Salamander Unk Desmognathus auriculatus Southern Dusky Salamander Unk Desmognathus f. -
The Behavioral Response of Larval Coastal Giant Salamanders, Dicamptodon Tenebrosus, to Chemical Stimuli
THE BEHAVIORAL RESPONSE OF LARVAL COASTAL GIANT SALAMANDERS, DICAMPTODON TENEBROSUS, TO CHEMICAL STIMULI By Larkin G. Chases A Thesis Presented to The Faculty of Humboldt State University In Partial Fulfillment of the Requirements for the Degree Master of Art In Biological Sciences May 2008 THE BEHAVIORAL RESPONSE OF LARVAL COASTAL GIANT SALAMANDERS, DICAMPTODON TENEBROSUS, TO CHEMICAL STIMULI by Larkin G. Chases Approved by the Master's Thesis Committee: John Reiss, Major Professor Date Michael Mesler, Committee Member Date Bruce O’Gara, Committee Member Date Richard Paselk, Committee Member Date Michael Mesler, Graduate Coordinator Date Chris Hopper, Interim Dean for Research and Graduate Studies Date ABSTRACT Nearly all animals are able to detect forms of chemical stimuli. In amphibians, chemoreceptive capabilities are used in a wide variety of contexts, including the detection of predators, conspecifics, and food. The focus of this project was the use of chemoreception in the feeding behavior of larval coastal giant salamanders, Dicamptodon tenebrosus. I investigated natural chemical cues used by larval salamanders to detect, locate, and assess potential food sources in a laboratory setting. Stimuli used in this study were as follows: bologna, agar blank, guano, lipid component of California black worms (Lumbriculus variegatus), cod liver oil, salt, and whole California black worms (Lumbriculus variegatus). All stimuli were housed in an agar-based morsel and presented to test subjects at the end of one arm in a Y-shaped test station. The results of this study provide substantial evidence of coastal giant larvae using chemical cues to detect, assess, and locate a food source. Test subjects actively investigated the test station during trials with all stimuli.