Spring Salamander (Gyrinophilus Porphyriticus) in Canada, Prepared Under Contract with Environment Canada
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
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. -
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. -
Northern Spring Salamander Fact Sheet
WILDLIFE IN CONNECTICUT STATE THREATENED SPECIES © COURTESY D. QUINN © COURTESY Northern Spring Salamander Gyrinophilus p. porphyriticus Background and Range The northern spring salamander is a brightly-colored member of the lungless salamander family (Plethodontidae). True to its name, it resides in cool water springs and streams, making it an excellent indicator of a clean, well- oxygenated water source. Due to its strict habitat and clean water requirements, it is only found in a handful of locations within Connecticut. The Central Connecticut Lowlands divide this amphibian's range into distinct populations. Litchfield and Hartford Counties support the greatest populations of spring salamanders. This salamander is listed as a threatened species in Connecticut. In North America, the spring salamander occurs from extreme southeastern Canada south through New England, west to Ohio, and south down the Appalachians as far as northern Georgia and Alabama. Description This large, robust salamander ranges in color from salmon to reddish-brown to purplish-brown, with a translucent white underbelly. The snout appears “square” when viewed from above and the salamander has well-defined grooves near its eyes to its snout. The tail is laterally flattened with a fin-like tip. Young spring salamanders are lighter in color and have small gills. Their coloration does not have deeper reddish tints until adulthood. Total length ranges from 5 to 7.5 inches. Habitat and Diet Spring salamanders require very clean, cool, and well-oxygenated water. They can be found in streams, brooks, and seepage areas. Preferred habitat lies within steep, rocky hemlock forests. This species is intolerant to disturbances. -
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. -
Cave Biodiversity of the Southern Cumberland Plateau Kirk S
b-3-guidebook_Guidebook3 6/18/2014 10:01 PM Page 159 Cave Biodiversity of the Southern Cumberland Plateau Kirk S. Zigler, NSS 62696; Matthew L. Niemiller, NSS 53235; and Danté B. Fenolio The South Cumberland Region of Tennessee, Alabama, and Georgia (Figure 1) is known for its tremendous diversity of caves, including huge pits, massive stream passages, and tight crawls. Less well known is that the region also supports tremendous cave biodiversity (Niemiller, Zigler, and Fenolio, 2013). Here we discuss many of the species that inhabit caves of the region, focusing on the southern Cumberland Plateau. Cave Biodiversity Four ecological classes of organisms can be found in caves: trogloxenes, subtroglophiles, eutroglophiles, and troglobionts (Culver and Pipan, 2009). Trogloxenes are not typically found in caves and cannot persist there for long periods of time. They must either find their way back to the surface or ultimately perish. Subtroglophiles are commonly found in caves but are associated with surface habitats for at least part of their life cycle. Some are seasonal inhabitants of caves and others move back and forth from cave to surface habitats for feeding, such as cave-roosting bats, cave crickets, and Allegheny Woodrats (Neotoma magister). Eutroglophiles are commonly found underground but can be found in surface habitats. Unlike trogloxenes and subtroglophiles, eutroglophiles can complete their entire life cycle Figure 1 - The South Cumberland Region at the junction of underground. Examples include the Cave Salamander Tennessee, Alabama, and Georgia. Figure courtesy of Nick Hollingshead. (Eurycea lucifuga) and the Cave Orbweaver (Meta ovalis). Troglobionts are obligate, permanent residents of subterranean habitats. -
Amphibian and Reptile Checklist
KEY TO ABBREVIATIONS ___ Eastern Rat Snake (Pantherophis alleghaniensis) – BLUE RIDGE (NC‐C, VA‐C) Habitat: Varies from rocky timbered hillsides to flat farmland. The following codes refer to an animal’s abundance in ___ Eastern Hog‐nosed Snake (Heterodon platirhinos) – PARKWAY suitable habitat along the parkway, not the likelihood of (NC‐R, VA‐U) Habitat: Sandy or friable loam soil seeing it. Information on the abundance of each species habitats at lower elevation. AMPHIBIAN & comes from wildlife sightings reported by park staff and ___ Eastern Kingsnake (Lampropeltis getula) – (NC‐U, visitors, from other agencies, and from park research VA‐U) Habitat: Generalist at low elevations. reports. ___ Northern Mole Snake (Lampropeltis calligaster REPTILE C – COMMON rhombomaculata) – (VA‐R) Habitat: Mixed pine U – UNCOMMON forests and open fields under logs or boards. CHECKLIST R – RARE ___ Eastern Milk Snake (Lampropeltis triangulum) – (NC‐ U, VA‐U) Habitat: Woodlands, grassy balds, and * – LISTED – Any species federally or state listed as meadows. Endangered, Threatened, or of Special Concern. ___ Northern Water Snake (Nerodia sipedon sipedon) – (NC‐C, VA‐C) Habitat: Wetlands, streams, and lakes. Non‐native – species not historically present on the ___ Rough Green Snake (Opheodrys aestivus) – (NC‐R, parkway that have been introduced (usually by humans.) VA‐R) Habitat: Low elevation forests. ___ Smooth Green Snake (Opheodrys vernalis) – (VA‐R) NC – NORTH CAROLINA Habitat: Moist, open woodlands or herbaceous Blue Ridge Red Cope's Gray wetlands under fallen debris. Salamander Treefrog VA – VIRGINIA ___ Northern Pine Snake (Pituophis melanoleucus melanoleucus) – (VA‐R) Habitat: Abandoned fields If you see anything unusual while on the parkway, please and dry mountain ridges with sandier soils. -
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. -
Distribution and Relative Abundance of Tennessee Cave Salamanders (Gyrinophilus Palleucus and Gyrinophilus Gulolineatus) with an Emphasis on Tennessee Populations
Herpetological Conservation and Biology 3(1):1-20. Submitted: 18 September 2007; Accepted: 28 December 2007 DISTRIBUTION AND RELATIVE ABUNDANCE OF TENNESSEE CAVE SALAMANDERS (GYRINOPHILUS PALLEUCUS AND GYRINOPHILUS GULOLINEATUS) WITH AN EMPHASIS ON TENNESSEE POPULATIONS 1,2 1,3 BRIAN T. MILLER AND MATTHEW L. NIEMILLER 1 Department of Biology, Middle Tennessee State University, Murfreesboro, Tennessee 37132, USA 2 Corresponding author, e-mail: [email protected] 3 Present Address: Department of Ecology and Evolutionary Biology, University of Tennessee, Knoxville, Tennessee 37996, USA, e-mail: [email protected] Abstract.—The Tennessee Cave Salamander complex (Gyrinophilus palleucus and G. gulolineatus) consists of three obligate cave-dwelling taxa inhabiting subterranean waters of east and central Tennessee, north Alabama, and northwest Georgia. Although ranges of these taxa are poorly understood, their populations are reportedly small and declining. The IUCN lists G. gulolineatus as "Endangered" and G. p. necturoides as "Vulnerable"; whereas, NatureServe lists G. gulolineatus (G1) and G. p. necturoides (G2G3T1) as Critically Imperiled. To better determine the distribution and relative abundance of extant populations, we searched 113 cave streams in middle and east Tennessee, seven in northwest Georgia, 13 in north Alabama and two in southern Kentucky. We found 1183 salamanders, including 63 G. gulolineatus, 681 G. palleucus, and 439 G. porphyriticus (Spring Salamanders), during 229 surveys of 135 caves. Gyrinophilus palleucus and G. gulolineatus were observed in more caves (30) than G. porphyriticus (17 caves). Members of the complex were found at 52% (12 of 23) of historic caves and at 16% (18 of 110) of non-historic caves. We extended the known distribution of G. -
Amphibian Habitat Usage of Two Restored Bogs in Shady Valley, Johnson County, Tennessee
East Tennessee State University Digital Commons @ East Tennessee State University Electronic Theses and Dissertations Student Works 8-2009 Amphibian Habitat Usage of Two Restored Bogs in Shady Valley, Johnson County, Tennessee. Amy P. Lucas East Tennessee State University Follow this and additional works at: https://dc.etsu.edu/etd Part of the Terrestrial and Aquatic Ecology Commons Recommended Citation Lucas, Amy P., "Amphibian Habitat Usage of Two Restored Bogs in Shady Valley, Johnson County, Tennessee." (2009). Electronic Theses and Dissertations. Paper 1785. https://dc.etsu.edu/etd/1785 This Thesis - Open Access is brought to you for free and open access by the Student Works at Digital Commons @ East Tennessee State University. It has been accepted for inclusion in Electronic Theses and Dissertations by an authorized administrator of Digital Commons @ East Tennessee State University. For more information, please contact [email protected]. Amphibian Habitat Usage of Two Restored Bogs in Shady Valley, Johnson County, Tennessee A thesis presented to the faculty of the Department of Biological Sciences East Tennessee State University In partial fulfillment of the requirements for the degree Master of Science in Biology by Amy P. Lucas August 2009 Dr. Fred Alsop, III – Chair Dr. Thomas Laughlin Dr. James Stewart Keywords: Amphibians, Salamanders, Shady Valley, Pitfall Trap ABSTRACT Amphibian Habitat Usage of Two Restored Bogs in Shady Valley, Johnson County, Tennessee by Amy P. Lucas Adjacent terrestrial habitat surrounding wetlands are critical for the survival and success of many species that use them. The primary purpose of this study was to determine amphibian movement from adjacent habitats into Orchard Bog, a restored bog located in Shady Valley, Johnson County, Tennessee. -
Common Name: TENNESSEE CAVE SALAMANDER Scientific Name: Gyrinophilus Palleucus Palleucus Mccrady Other Commonly Used Names: Pa
Common Name: TENNESSEE CAVE SALAMANDER Scientific Name: Gyrinophilus palleucus palleucus McCrady Other Commonly Used Names: pale salamander Previously Used Scientific Names: none Family: Plethodontidae Rarity Ranks: G2G3/S1 State Legal Status: Threatened Federal Legal Status: none Description: The Tennessee cave salamander is a moderately sized, paedomorphic salamander (10 - 24 cm [4 - 9½ inches] in total length) that retains gills throughout life. Adult dorsal coloration is variable, ranging from an immaculate pale brown or pink to beige or brown with some populations possessing black spots. The belly is paler than the dorsum. Juveniles of this species are pale and lack spots. The eyes are small, and the head is long with a squared-off, spatulate snout. Gills are typically reduced, stubby, and pale; however, they may be bright red and bushy, particularly when stressed. A well-developed lateral-line system with noticeably unpigmented, sensory pores is present, and the tail is flattened from side to side with a well- developed fin. Similar Species: The eyes of Tennessee cave salamander are noticeably smaller than those of the closely related spring salamander ( Gyrinophilus porphyriticus ). In Tennessee cave salamander, the diameter of the eye is less than 25% of the length of the snout; whereas in spring salamander, the diameter of the eye is greater than 30% of the snout length. Molecular evidence suggests that the Frick's Cave population is unique from other cave-dwelling Gyrinophilus in the region. Habitat: The Tennessee cave salamander inhabits subterranean water and is generally found in cave streams. Populations with relatively high density are associated with inflowing streams and a concomitant increase in organic matter. -
Baseline Survey and Habitat Analysis of Aquatic Salamanders in the Pigeon River, North Carolina
University of Tennessee, Knoxville TRACE: Tennessee Research and Creative Exchange Masters Theses Graduate School 12-2009 Baseline survey and habitat analysis of aquatic salamanders in the Pigeon River, North Carolina Nikki J. Maxwell The University of Tennessee-Knoxville, [email protected] Follow this and additional works at: https://trace.tennessee.edu/utk_gradthes Part of the Biology Commons Recommended Citation Maxwell, Nikki J., "Baseline survey and habitat analysis of aquatic salamanders in the Pigeon River, North Carolina. " Master's Thesis, University of Tennessee, 2009. https://trace.tennessee.edu/utk_gradthes/545 This Thesis is brought to you for free and open access by the Graduate School at TRACE: Tennessee Research and Creative Exchange. It has been accepted for inclusion in Masters Theses by an authorized administrator of TRACE: Tennessee Research and Creative Exchange. For more information, please contact [email protected]. To the Graduate Council: I am submitting herewith a thesis written by Nikki J. Maxwell entitled "Baseline survey and habitat analysis of aquatic salamanders in the Pigeon River, North Carolina." I have examined the final electronic copy of this thesis for form and content and recommend that it be accepted in partial fulfillment of the equirr ements for the degree of Master of Science, with a major in Wildlife and Fisheries Science. J. Larry Wilson, Major Professor We have read this thesis and recommend its acceptance: Matthew J. Gray, Lisa I. Muller Accepted for the Council: Carolyn R. Hodges Vice Provost and Dean of the Graduate School (Original signatures are on file with official studentecor r ds.) To the Graduate Council: I am submitting herewith a thesis written by Nikki J.