An adult Western Ratsnake from Johnson County. © Jessica Lawrenz.
An adult Western Ratsnake from Linn County, Kansas. © Suzanne L. Collins, CNAH.
An adult Western Ratsnake from Marshall County. © Lisa Wehrly.
An adult Western Ratsnake consuming a domestic chicken egg in Atchison County. Image © Mark McDaniel.
An adult Western Ratsnake from Shawnee County. © Emery Forrest.
An adult Western Ratsnake from Cherokee County, Kansas. Image © Lisa Wehrly.
An adult Western Ratsnake from Chautauqua County, Kansas. Image © Dan Fogell.
Head of a juvenile Western Ratsnake from Butler County. Image © Jennifer Breitkreutz.
REPTILIA (Reptiles) SQUAMATA (PART) (Snakes) COLUBRIDAE (Harmless Egg-laying Snakes)

Western Ratsnake
Pantherophis obsoletus (Say in James, 1822: 140)
păn-thŭr-ō-fĭs — ŏb-sō-lē-tŭs


Conservation Status:

State: None

Federal: None
NatureServe State: S5 - Secure
NatureServe National: N5 - Secure
NatureServe Global: G5 - Secure
CITES: None
Diagnosis:
HARMLESS. One of the largest snakes in Kansas, the Western Ratsnake is characterized by keeled scales, a divided anal scale, and a generally uniform dark brown or black color on the head, body, and tail. Some adult specimens exhibit an indistinct pattern of dark blotches, and those in south central Kansas may be distinctly blotched. Adults often have extensive red and white (sometimes yellow) colored skin between the scales. The belly is cream or yellow-white, with large indistinct darker areas and may have an overall yellowish to reddish cast. Young specimens are patterned and colored similarly to Great Plains Ratsnakes, but they lose this pattern as they grow older. The blotches on a young Western Ratsnake will be longer than they are wide and often have small projections toward the head and the tail from each corner (on a Great Plains Ratsnake, they will be wider than they are long).The edges of the blotches are not darker than their centers. Young Western Ratsnakes begin to darken appreciably (obfuscating their juvenile pattern) in their third year.
The degree of dorsal darkening varies from completely black individuals throughout most of the state to faintly blotched specimens in south-central Kansas (Miller, 1986, Irwin et al., 1992). Adult males have slightly longer tails and grow larger than females.
Adults normally grow 106.7-183.0 cm (42-72 inches) in total length. The largest specimen from Kansas is a male (KU 216168) from Jefferson County with a total length of 191.2 cm (75­1⁄8 inches) and a weight of 1,729 grams (3 pounds, 13 ounces), collected by Roger Christie on 9 July 1990. The maximum length throughout the range is 218.4 cm (85‌49⁄50 inches) (Boundy, 1995; Powell et al., 2016).

Distribution:
Widely distributed in the more forested eastern half of the state, On the western edge of its range, it is found along riparian corridors. They are commonly found in abandoned buildings and barns and are often the most common large snake in suburban areas.
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Full range depicted by light shaded red area. Export Google Earth (.kml)
  • Occurrence Summary:  
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    Records 
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    Other Observations 
Some county occurrences indicated below may be too imprecise to map above.
County Breakdown: County Name (# occurrences):


Fossil History:
Pleistocene fossil specimens are known from the Borchers (Hibbard, 1970), Deer Park (Hibbard, 1956), Fox Canyon (Hibbard, 1950), Jinglebob, Jones (Ranch), Rexroad (location 3) (Hibbard, 1970), and Wendell Fox Pasture (Hibbard and Bjork, 1971) local faunas of Meade County [currently extralimital], Saw Rock local fauna of Seward County [currently extralimital] (Hibbard,1964), Kentuck local fauna of McPherson County, and Dixon local fauna of Kingman County (Brattstrom, 1967; Holman, 1995).

Natural History:
Gloyd (1928) and Fitch (1956, 1958, 1963) studied this snake in eastern Kansas. The Western Ratsnake generally inhabits forested areas, particularly the rocky hillsides of open woodlands. Along the western edge of its range, it frequents the wooded areas of streams and rivers. These snakes are active from late March to November at air temperatures of 60-88°F. Like many other snakes, this species is primarily active by day during spring and fall but becomes more nocturnal during the hot summer. Western Ratsnakes have home ranges of 10.1 to 12,1 hectares (25-30 acres); they prowl these regions, frequently climbing trees in search of food. Schmidt (1941) stated that Gloyd observed them 3 to 9.1 meters (10 to 30 feet ) above the ground among the branches of trees. Population density is approximately one snake per three acres.
During fall, the Western Ratsnake retreats to den sites on rocky, wooded hillsides which it may share with many other kinds of snakes. It spends the winter months in burrows on these hillsides avoiding cold temperatures. Miller (1977) reported an adult example of this snake active on 9 February in Sumner County; the day was warm and sunny. During an unseasonably mild spell, Capron (1986) observed Western Ratsnakes active in January and February near Oxford.
The Western Ratsnake usually mates in spring, but occasional unions may occur throughout the annual activity period. Gillingham (1979) reported a three-phase courtship behavior similar to that of the Great Plains Western Ratsnake (see preceding account), except that male Western Ratsnakes may bite females prior to copulation. The eggs, which range in number from six to 44 per clutch (Fitch, 1985), are laid beneath or in logs or in moist soil under rocks during June or July. The eggs hatch in one to two months.
Western Ratsnakes constrict their prey and feed on frogs, lizards, snakes, bird eggs, birds, rodents, and rabbits. Henderson (1974) recorded Douglas County examples of this snake eating frogs, birds, and small mammals. Plummer (1977) reported heavy predation by this snake on bank swallows ·along the Kansas River in the same county. This snake frequently robs bird nests, and provokes heckling by concentrations of birds. Blue Jays have been known to attack Western Ratsnakes during nest robbing. Linsdale (1925) reported predation of a Blue Jay nest on 11 July 1923. Cary et al. (1981) reported predation on a bat in Texas County, Missouri. Juveniles eat small frogs, lizards, and small rodents. They are adept climbers. William L. Hoyle discovered a moderate-sized specimen in the cupola of a barn near Grenola (Elk County), Kansas on 29 July 1933 that was consuming the eggs of an English Sparrow (Burt and Hoyle, 1935). Upon subsequent dissection, it was determined adult female English Sparrow was consumed at the same time.
Hawks are the main predator of the Western Ratsnake in Kansas, though it is preyed upon by mammals and other snakes as well (Collins, 1993). Hawks, in particular, easily locate this snake when it is being heckled by other birds during nest raiding. Capron (1985) recorded 53 of these snakes killed by swathing (mowing) machines during agricultural harvests from May to mid-July in southern Kansas.

Occurrence Activity:
Remarks:
This was the first species of amphibian or reptile to be documented in what we can be sure was Kansas (but in an unfortunate twist of politics that all changed) (Taggart 2021).
Thomas Say (1823) described the type specimen of the Western Ratsnake from Isle au Vache (Cow Island), Kansas (a heavily forested island on the Missouri River). His type locality stretches from NE Kansas to western Iowa. Say wrote... "It is not an uncommon species on the Missouri from the vicinity of Isle au Vache to Council Bluff.".
Cow Island was the site of Cantonment Martin, a military camp established as a supply base for Major Stephen H. Long’s engineering expedition of 1819-20 of which Say served as the naturalist. This expedition set out to survey the Rocky Mountains and the major tributaries of the Missouri River.
A flood in 1881 shifted the main channel of the Missouri River west and Cow Island became connected to the Missouri side. For several years, both Kansas and Missouri lay claim to the land that had been Cow Island and the dispute was ultimately settled in 1890 when a court ruled that a boundy would change with the gradual movement of a natural boundary (accretion) but not due to a sudden change (avulsion). Therefore, the land still belonged to Kansas and would for most of the next 60 years.
The Kansas, Missouri, and the US Congress ratified the Kansas-Missouri Boundary compact in 1949 which set the boundary at the center of the current channel of the Missouri River (which by then had been dredged, levied, and straightened so as to become effectively fixed)... and Kansas lost its first type locality.
The oldest existing specimen is in the Royal Ontario Museum (ROM 4228) and was collected in 1886 (no other associated data).
This species exhibits an ontogenetic color shift as it matures. Newborn individuals are light gray with well-defined dark blotches. In their second year, the pattern begins to be obscured as the snake transitions to an overall dark animal.
Specimens from the southwestern portion of its range in the state show a propensity for maintaining more of their blotched pattern as adults (Miller, 1986, Irwin et al., 1992).
Based on the congruence of morphological (Burbrink, 2001, Herpetol. Monogr. 15: 1–53) and mitochondrial data (Burbrink et al., 2000, Evolution 54: 2107–2118), Burbrink divided P. obsoletus into three species (P. alleghaniensis, P. obsoletus and P. spiloides) with no subspecies. Burbrink (2020) further supported the recognition of P. obsoletus as a taxon distinct from P. alleghaniensis and P. spiloides), but see Hillis and Wuster (2021). While not affecting P. obsoletus (and therefore those populations in Kansas), Burbrink (2021) noted that P. alleghaniensis should actually apply to the middle lineage (geographically; east of the Mississippi River and west of the Appalachians and Flint/Apalachicola rivers) and the oldest available name for the eastern lineage is P. quadrivittatus.
Hillis (2022) further the debated the status (specific vs. subspecific) of the Pantherophis obsoletus complex across eastern North America. He argued specifically that Burbrink et al. (2020) demonstrated a wide intergrade zone with no apparent breaks due to reproductive/genetic barriers between the their putative P. alleghaniensis, P. quadrivittatus, and P. obsoletus. There is no standard measure as to what point a hybrid/intergrade zone becomes sufficiently wide to determine if the two (or more) constituent populations are species or 'subspecies'. Nor should there be, as doing so would denigrate the delineation of real species to an arbitrary class threshold (Frost and Hillis, 1990). Hillis (2022) further argues that the reasoning (in part) invoked by Burbrink et al. (2021) for elevating P. alleghaniensis, P. quadrivittatus, and P. obsoletus; (specifically that as P. bairdi and P. obsoletus share a more recent common ancestor with each other than either does with P. alleghaniensis or P. quadrivittatus; recognizing P. bairdi and the remaining taxa as subspecies of P. obsoletus, would render P. obsoletus paraphyletic) is likely due to hybridization. However, all phylogenetic hypotheses are generated from gene data and as such are subject to being misled by xenologous/paralogous relationships of those genes with respect to the true phylogeny (which is unknowable).
Utiger et al. (2002, Russian J. Herpetol. 9: 105–124), using molecular data, divided Elaphe into eight genera. New World Elaphe are part of a clade distinct from Old World species, for which Pantherophis Fitzinger, 1843, was resurrected as the oldest available name. Further splitting of Pantherophis has been proposed (Collins and Taggart, 2008).
On the map (Carte itineraire de Prince Maximilian de Wied dans l'interieur de l'Amerique Septentrionale de Boston a Missouri superieur &c. en 1832, 33 et 34) accompanying the report of Prince Maximilian zu Weid's explorations in North America the area of Doniphan County, north and west of Wathena, is labeled "Wa-con-se-nac or Black Snake Hills".

Bibliography:
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Travis W. Taggart © 1999-2025 — w/ Sternberg Museum of Natural History, Fort Hays State University