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	Conservation Status (definitions)
IUCN (Red List) Status	Vulnerable (VU) See IUCN account.
NatureServe Status	Use NatureServe Explorer to see status.
CITES	No CITES Listing
Other International Status	None
National Status	None
Regional Status	Florida/Georgia: Endangered

Description
Description: Ambystoma bishopi is a moderately sized salamander species. The snout-vent length (SVL) of A. bishopi males ranges from 40.52-47.08 mm.Adult females have an SVL range of 41.09- 51.17 mm. 14 to 16 costal grooves are present. Tail width and height are sexually dimorphic characters, both of which are smaller in males (Pauly et al. 2007). The skin is smooth dorsally and ventrally, but is wrinkled on the flanks between the axilla and groin. The head is elongate. The snout is tapered. The nostrils are small and located towards the tip of the snout. Eyes are of medium size. A groove goes from the corner of the eye to behind the jaw base (Goin 1950).This species has vomerine teeth. However the arrangement and number are debated. Goin (1950) states the teeth are uniformly arranged into two rows while another study claims variable rows of teeth arrangement (Martof and Gerhardt 1965). The forelimbs are stout. The tail is flattened posteriorly and is shorter than the head and body lengths (Goin 1950).

Diagnosis: A. bishopi can be distinguished from A. cingulatum by its shorter limbs and smaller head (USFWS 2009). Generally, this species has fewer costal grooves than A. cingulatum and a shorter tail. The ventral pattern of A. bishopi consists of indistinct white spots on a dark background, creating a "salt and pepper" look, compared to A. cingulatum, which has distinct white spots on the ventral side (Goin 1950; USFWS 2009). The dorsal side pattern of A. bishopi is more net-like in appearance than the frosted patterning of A. cingulatum (USFWS 2009; Goin 1950).

Tadpole morphology: Larvae are less vividly marked and metamorphose earlier and at a smaller size than A. cingulatum (Goin 1950; Telford 1954). A. bishopi has several stripes either yellow brown or black along the body. Gills are bright red in life (Telford 1954).

A. bishopi and A. cingulatum larvae are difficult to distinguish (Martof and Gerhardt 1965). A. cingulatum larvae have broad, striped heads, with a black stripe extending from the nose to the gills and a second stripe along the upper jaw (Palis 1996). A light lateral stripe is retained in first year fully metamorphosed individuals, but is lost in older individuals (Palis 1997).

Coloration: The dorsal surface of A. bishopi is reticulated, with thin grey lines that form a net-like or banded pattern against a black to brown background (USFWS 2009). These lines surround areas of dark coloration (Martof and Gerhardt 1965). Small white flecks on a dark background cover the ventral surface, creating a "salt and pepper" pattern (Goin 1950). Preserved specimens of A. bishopi, can become dark, making their dorsal pattern unrecognizable (Martof and Gerhardt 1965).

Distribution and Habitat

Country distribution from AmphibiaWeb's database: United States

U.S. state distribution from AmphibiaWeb's database: Alabama, Florida, Georgia

View distribution map using BerkeleyMapper.

Historically, A. bishopi was distributed west of the Apalachicola-Flint River, in the lower Gulf coastal plains of southern Alabama, Georgia, and Northern Florida (Pauly et al. 2007; Whiles et al. 2004). Currently, their known distribution includes portions of the Florida panhandle and southern Georgia, west of the Apalachicola-Flint River (Pauly et al. 2007). No members of this species have been found in Alabama since 1981 (Godwin pers. comm).

Habitat for mature salamanders consists of upland areas with few tress, typically longleaf pines, and grasses. Soil is poorly drained sand, which leads to seasonal ponds and damp surroundings. This habitat will often have an open overstory of widely scattered longleaf pine, little to no midstory, and a diverse community of low growing shrubs which include highly diverse forb and grass communities (Palis 1996).

Larval A. bishopi occupy acidic (pH 3.4 - 5.6) ephemeral wetlands. These wetlands have varying amounts of vegetation, and lack dense midstory growth. Canopy is comprised of a typical Florida wetland assemblage (Palis 1996).

Life History, Abundance, Activity, and Special Behaviors
A. bishopi is a terrestrial, burrow-dwelling salamander that spends the majority of its life among the leaf litter. It emerges from the ground at night during periods of rain to breed (Palis 1996). These migrations have been linked to the presence of cold fronts. The breeding migration begins in October as heavy rains draw adults out (Palis 1997).

Females lay a number of eggs proportional to their size but may produce up to 225 eggs. Eggs are deposited either individually or in small groups beneath leaf litter, logs, shrubs, trees or at the entrance to crayfish burrows before breeding sites begin to fill up (Anderson and WIlliamson 1976; Palis 1996). Eggs may develop to hatching size within three weeks but will not actually hatch until flooded with water. Larvae are nocturnal, hiding most of the day, and feeding in a water column at night. Metamorphosis usually takes place beginning in March and ends in April (Palis 1996). Mature salamanders move to upland areas where they live until returning to ponds to breed (USFWS 2009).

Adults of A. bishopi have been known to consume earthworms while larvae feed on invertebrates, such as crustaceans, isopods (Caecidotea) and amphipods (Crangonyx) (Goin 1950; Whiles et al. 2004).

Trends and Threats
Habitat loss from agricultural conversion or commercial development, pond alteration and additional introduction of predatory fish, fire suppression leading to altered forest habitat and crayfish harvesting comprise the most serious threats to A. bishopi populations (Palis and Hammerson 2008). One threat comes from the introduction of predators or disease to their small breeding pools from larger, permanent water sources via roadside ditches, tire ruts or other such manmade disturbances. "Red-leg" disease (Aeromonas hydrophila) is known to have affected A. talpoideum populations in breeding pools A. bishopi also historically occupied. Chytrid fungus (Batrachochytrium dendrobatidis) and a parasitic nematode (Hedruris siredonis) have also been associated with decreased larval fitness and mass die-offs in other Ambystomatid species, suggesting that they could also pose a threat to A. bishopi. An estimated 36 percent of all known populations have only one breeding pond that they use annually and any disruption could lead to a severe decline (USFWS 2009).

A. bishopi selectively breeds in open canopy, longleaf pines which are particularly fire-adapted. However, fire suppression may lead to changes in the coverage and wetland composition that this species selects for. Further growth could crowd the ecosystem and destroy historical breeding ponds (Bishop and Haas 2005). Though this has not been proven, the potential exists if no consideration is given.

Due to the burrowing nature of the species, adult population numbers are difficult to enumerate. However, no more than 10,000 adults in twenty populations are estimated within the entire range. The population is assumed to be declining rapidly given deforestation, silviculture, and general habitat degradation and fragmenting (Palis and Hammerson 2008).

Possible reasons for amphibian decline

General habitat alteration and loss
Habitat modification from deforestation, or logging related activities
Intensified agriculture or grazing
Urbanization
Disturbance or death from vehicular traffic
Drainage of habitat
Subtle changes to necessary specialized habitat
Habitat fragmentation
Local pesticides, fertilizers, and pollutants
Disease

Comments
Species Authority and Phylogenetic Relationships: A. bishopi was first described by Goin (1950) as Ambystoma cingulatum bishopi. Later this subspecies categorization was refuted by Martof and Gerhardt (1965) and was combined with A. c. cingulatum to form one species, A. cingulatumi. In 2007, A. bishopi was separated from A.cingulatum by Pauly et al. (2007) based on differences in mitochondrial DNA, morphology and allozymes. Because the two species were considered subspecies until 2007 and much of the life history information is assumed to be true for both species (USFWS 2009).

References
 

Anderson, J. D., and Williamson, G. K. (1976). ''Terrestrial mode of reproduction in Ambystoma cingulatum.'' Herpetologica, 32, 214-221.  

Bishop, D.C, Haas, C.A. (2005). ''''Burning trends and potential negative effects of suppressing wetland fires on flatwoods salamanders.'' Natural Areas Journal , 25, 290-294.  

Goin, C. J. (1950). ''A study of the salamander, Ambystoma cingulatum, with the description of a new subspecies.'' Annals of the Carnegie Museum, 31, 229-321.  

Martof, B. S., and Gerhardt, H. C. (1965). ''Observations on the geographic variation in Ambystoma cingulatum.'' Copeia, 1965, 342-346.  

Palis, J. G. (1997). ''Breeding migration of Ambystoma cingulatum in Florida.'' Journal of Herpetology, 31, 71-78.  

Palis, J., Hammerson, G. 2008. Ambystoma cingulatum. In: IUCN 2011. IUCN Red List of Threatened Species. Version 2011.2. www.iucnredlist.org. Downloaded on 15 March 2012.  

Palis, J.G. (1996). ''Flatwoods Salamander (Ambystoma cingulatum Cope). Element stewardship abstract.'' Natural Areas Resource Journal, 16, 49-54.  

Pauly, G.B., Piskurek, O., Shaffer, H.B. (2007). ''Phylogeographic concordance in the southeastern United States: the flatwoods salamander, Ambystoma cingulatum, as a test case.'' Molecular Ecology, 16, 415-429.  

Telford, S. R. (1954). ''A description of the larvae of Ambystoma cingulatum bishopi Goin. including an extension of the range.'' Quarterly Journal of the Florida Academy of Sciences, 17, 233-236.  

United States Fish and Wildlife Service (USFWS) (2009). ''Determination of endangered status for Reticulated Flatwoods Salamander.'' Federal Register, 74(26), 6700-6774.  

Whiles, M. R., Jensen, J. B., and Palis, J. G. (2004). ''Diets of larval flatwoods salamanders, Ambystoma cingulatum, from Florida and South Carolina.'' Journal of Herpetology, 38, 208-214.

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