Opheodrys aestivusRough greensnake

Ge­o­graphic Range

Opheodrys aes­tivus, com­monly known as the rough green snake, is found widely through­out the south­east­ern United States. It is found fre­quently as far north as south­ern New Jer­sey and can be found along the East Coast into the Florida Keys. The west­ern range stretches to cen­tral Ok­la­homa, Texas, and into north­ern Mex­ico. (Gray, 2005; Mitchell, 1994)

Habi­tat

Rough green snakes are typ­i­cally found on for­est edges near ponds or lakes. Al­though they are ar­bo­real snakes, they for­age in dense veg­e­ta­tion along pond and lake shore­lines dur­ing the day. Their nights are spent coiled in the branches of trees. Rough green snakes choose perches based on dis­tance from shore­lines, height in branches, and thick­ness of the branch. Rough green snakes are most com­monly found in de­cid­u­ous trees, shrubs, hedgerows, and fields. (Mitchell, 1994; Plum­mer, 1981; Plum­mer, 1997a)

Phys­i­cal De­scrip­tion

Rough green snakes are small and thin. The dor­sal and lat­eral sur­faces are a uni­form green, the un­der­belly, chin and labial scales range from yel­low­ish-green to cream. Males and fe­males have no dif­fer­ences in color or pat­tern, but fe­males are larger in length and mass, while males have a longer tail length. Ju­ve­nile rough green snakes look like smaller adults, ex­cept they are lighter in color. Since these snakes are di­ur­nal and tend not to avoid the heat of the day, their peri­toneum is black and dense. This is be­lieved to be an adap­ta­tion that acts as an ul­tra­vi­o­let ra­di­a­tion shield, keep­ing these snakes from be­com­ing too hot. Fe­males range from 11 to 54 g in mass, with an av­er­age of 26.7 g, males are from 9 to 27 g, with an av­er­age of 16.3 g. Av­er­age lengths are 947 mm in fe­males and 892 mm in males. (Mitchell, 1994; Plum­mer, 1993)

  • Sexual Dimorphism
  • sexes alike
  • female larger
  • Range mass
    female: 11 male: 9 to female: 54 male: 27 g
    to oz
  • Average mass
    female: 26.7 male: 16.3 g
    oz
  • Average length
    female: 947 male: 892 mm
    in

De­vel­op­ment

When com­pared to other snakes, Opheodrys aes­tivus em­bryos are well-de­vel­oped upon egg lay­ing. This al­lows for a short in­cu­ba­tion pe­riod out­side of the fe­male, thus short­en­ing the span for preda­tors to eat the de­fense­less eggs. These eggs usu­ally range from 21.4 to 33.6 mm long, 9.3 to 11.1 mm wide, and 1.2 to 2.4 g. Upon hatch­ing, their length av­er­ages 128 to 132 mm and weigh 1.1 g (Mitchell, 1994). Most growth oc­curs in the first year of life. Fe­males grow at a faster pace and reach larger sizes than males. Ac­cord­ing to Plum­mer (1985), the growth of rough green snakes fol­lows the Von Berta­lanffy model, which al­lows any size snake to be aged rel­a­tively ac­cu­rately. How­ever, this model is more ac­cu­rate for younger snakes; error is pos­i­tively cor­re­lated with age. (Mitchell, 1994; Plum­mer, 1985a)

Re­pro­duc­tion

Rough green snakes re­pro­duce sex­u­ally with in­ter­nal fer­til­iza­tion. These snakes are promis­cu­ous, with males leav­ing al­most im­me­di­ately after cop­u­la­tion (Rich­mond, 1956). Courtship be­hav­ior of rough green snakes con­sists of vi­sual ori­en­ta­tion of males to­wards fe­males, ap­proach, body con­tact, and body align­ment. Some motor pat­terns that are dis­played dur­ing these stages are dor­sal crawl­ing, chin rub­bing, tail wav­ing, and head jerk­ing. Once aligned with a fe­male, a male be­gins with tail search cop­u­la­tory at­tempts in en­er­getic spurts fol­lowed by pe­ri­ods of mo­tion­less­ness. On av­er­age, align­ment is ac­com­plished in about 2:45 min­utes and the cop­u­la­tory se­quences av­er­age about 16:04 min­utes (Gold­smith, 1988). (Gold­smith, 1988; Mitchell, 1994; Rich­mond, 1956)

Rough green snakes reach sex­ual ma­tu­rity at 21 months in males and 21 to 33 months in fe­males (Plum­mer, 1985). Al­though they breed every spring, fall mat­ings have been noted (Mitchell, 1994). The ges­ta­tion pe­riod can range from 5 to 12 weeks, de­pend­ing on tem­per­a­tures, and they typ­i­cally lay their eggs dur­ing June and July (Plum­mer, 1990). Clutch size is 3 to 12 soft-shelled eggs (Mitchell, 1994). Males first breed in the spring of their sec­ond year, usu­ally around 21 months. How­ever only half of fe­males par­tic­i­pate in breed­ing dur­ing their sec­ond spring, while the other half de­lays an ad­di­tional 12 months. Re­pro­duc­tively ma­ture fe­males can range from 360 to 400 mm snout-vent length, while sex­u­ally-ma­ture males av­er­age 300 mm (Plum­mer, 1985). (Gold­smith, 1984; Mitchell, 1994; Plum­mer, 1985a; Plum­mer, 1990a)

  • Breeding interval
    Breeding occurs once yearly.
  • Breeding season
    Rough green snakes breed in the spring.
  • Range number of offspring
    3 to 12
  • Average number of offspring
    6.2
  • Range gestation period
    5 to 12 weeks
  • Average gestation period
    6 weeks
  • Range age at sexual or reproductive maturity (female)
    21 to 33 months
  • Range age at sexual or reproductive maturity (male)
    20 to 21 months
  • Average age at sexual or reproductive maturity (male)
    21 months

Fe­male rough green snakes near­ing ovipo­si­tion leave their usual ar­bo­real habi­tat to travel on the ground away from the shore­line. They seek out hol­lows in dead or liv­ing trees, de­cay­ing logs, under rocks or under boards in sandy soil. Such areas pro­vide suf­fi­cient mois­ture lev­els for egg-lay­ing. These lo­ca­tions are usu­ally about 30.0 m (+/- 9.0 m) away from the shore­line. After ovipo­si­tion, fe­males re­turn to the shore­line and re­sume her ar­bo­real post. Fe­males have no fur­ther con­tact with their eggs after hatch­ing (Plum­mer, 1990). (Plum­mer, 1990b)

  • Parental Investment
  • no parental involvement
  • pre-fertilization
    • protecting
      • female
  • pre-hatching/birth
    • provisioning
      • female
    • protecting
      • female

Lifes­pan/Longevity

Sur­vival rates are not well known for ju­ve­nile rough green snakes. How­ever, adults have low sur­vivor­ship, which may partly ex­plain why these snakes be­come sex­u­ally ma­ture early and lay rather large clutches an­nu­ally. The main causes of mor­tal­ity are en­vi­ron­men­tal fac­tors (hot, dry con­di­tions) and pre­da­tion. This species has an av­er­age life ex­pectancy of 5 years, but they can reach up to 8 years. (Gold­smith, 1984; Plum­mer, 1985b; Plum­mer, 1997a; Plum­mer, 1997b)

  • Average lifespan
    Status: wild
    8 years
  • Typical lifespan
    Status: wild
    8 (high) years
  • Average lifespan
    Status: wild
    5 years

Be­hav­ior

Rough green snakes are ar­bo­real and di­ur­nal. They spend their nights coiled on the far ends of tree branches near the shore­line (Plum­mer, 1997). Al­though ar­bo­real, they spend time on the ground for­ag­ing. They are seden­tary and will not bite as a de­fense, but rather flee into dense veg­e­ta­tion where they are cam­ou­flaged (Mitchell, 1994). Rough green snakes are ac­tive ex­cept in the cold win­ter months, usu­ally De­cem­ber to Feb­ru­ary, de­pend­ing on ge­o­graphic lo­ca­tion and tem­per­a­ture (Mitchell, 1994). The cold months are spent in hi­ber­na­tion. Rough green snakes are soli­tary, but there is a pos­si­bil­ity that they use com­mu­nal egg-lay­ing (Palmer & Braswell, 1976). (Mitchell, 1994; Palmer and Braswell, 1976; Plum­mer, 1997a)

  • Average territory size
    201 m^2

Home Range

Rough green snakes have a home range of roughly 67 m in shore length, while only stray­ing about 3 m away from the shore it­self. Home ranges vary year to year by about 50 m (Plum­mer, 1997). They are not ter­ri­to­r­ial. (Mitchell, 1994; Plum­mer, 1997a)

Com­mu­ni­ca­tion and Per­cep­tion

Rough green snakes use their tongue to sense chem­i­cal cues. They also have keen eye­sight, al­low­ing them to eas­ily spot move­ment of prey. Mat­ing be­hav­iors in­volve tac­tile and vi­sual cues. (Cooper, 2007)

Food Habits

Rough green snakes are in­sec­ti­vores, con­sum­ing crick­ets, grasshop­pers, other in­sects, and spi­ders (Mitchell, 1994). They ex­clu­sively use their ex­tra­or­di­nary vi­sion to hunt live prey. Even a slight move­ment of a leg or an­ten­nae is suf­fi­cient to draw the at­ten­tion of these snakes to the lo­ca­tion of their prey (Gold­smith, 1986). Ac­cord­ing to Gold­smith (1986), dur­ing the ini­tial phase of their ap­proach, these snakes use fast and ir­reg­u­lar move­ments, but they slow down as they fur­ther ap­proach their prey. When rough green snakes are about 3 cm from prey, they as­sume spring-like curves with their body, fol­lowed by a straight­en­ing of the body, al­low­ing the snake to pro­pel its head to­ward the prey, strik­ing ei­ther at the head or tho­rax. Rough green snakes some­times raise their head above the sub­strate im­me­di­ately upon strik­ing in order to get prey away from any­thing that may aid their es­cape. Prey is worked fur­ther into the mouth and swal­lowed by move­ments of the jaw. Prey is usu­ally swal­lowed head first. (Gold­smith, 1986; Mitchell, 1994)

  • Animal Foods
  • insects
  • terrestrial non-insect arthropods

Pre­da­tion

Many an­i­mals prey up on these snakes, in­clud­ing larger snakes, birds, do­mes­tic cats, and even some spi­ders (Plum­mer, 1990; Mitchell, 1994). Their only de­fense mech­a­nism is cam­ou­flage. (Mitchell, 1994; Plum­mer, 1990a)

  • Anti-predator Adaptations
  • cryptic

Ecosys­tem Roles

Rough green snakes are a source of prey for larger snakes, birds, and other small preda­tors. There are a few known par­a­sites that af­fect rough green snakes. They are in­fected oc­ca­sion­ally with Cryp­tosporid­ium species, which af­fects the gas­troin­testi­nal tract, caus­ing ep­ithe­lial necro­sis. (Brower and Cran­field, 2001; Plum­mer, 1981)

Com­men­sal/Par­a­sitic Species
  • Cryp­tosporid­ium species

Eco­nomic Im­por­tance for Hu­mans: Pos­i­tive

Al­though not com­mon pets, do­mes­ti­ca­tion of these snakes has be­come in­creas­ingly pop­u­lar be­cause they are easy to care for. (Plum­mer, 1981)

Eco­nomic Im­por­tance for Hu­mans: Neg­a­tive

There are no known ad­verse ef­fects of Opheodrys aes­tivus on hu­mans.

Con­ser­va­tion Sta­tus

Rough green snakes are listed as a species of least con­cern. Due to their ap­par­ent pop­u­la­tion sta­bil­ity, no con­ser­va­tion ef­forts are planned. (Plum­mer, 1985b)

Con­trib­u­tors

Kaelin Cre­ange (au­thor), Rad­ford Uni­ver­sity, Karen Pow­ers (ed­i­tor), Rad­ford Uni­ver­sity, Tanya Dewey (ed­i­tor), Uni­ver­sity of Michi­gan-Ann Arbor.

Glossary

Nearctic

living in the Nearctic biogeographic province, the northern part of the New World. This includes Greenland, the Canadian Arctic islands, and all of the North American as far south as the highlands of central Mexico.

World Map

arboreal

Referring to an animal that lives in trees; tree-climbing.

carnivore

an animal that mainly eats meat

chemical

uses smells or other chemicals to communicate

cryptic

having markings, coloration, shapes, or other features that cause an animal to be camouflaged in its natural environment; being difficult to see or otherwise detect.

diurnal
  1. active during the day, 2. lasting for one day.
heterothermic

having a body temperature that fluctuates with that of the immediate environment; having no mechanism or a poorly developed mechanism for regulating internal body temperature.

hibernation

the state that some animals enter during winter in which normal physiological processes are significantly reduced, thus lowering the animal's energy requirements. The act or condition of passing winter in a torpid or resting state, typically involving the abandonment of homoiothermy in mammals.

insectivore

An animal that eats mainly insects or spiders.

iteroparous

offspring are produced in more than one group (litters, clutches, etc.) and across multiple seasons (or other periods hospitable to reproduction). Iteroparous animals must, by definition, survive over multiple seasons (or periodic condition changes).

native range

the area in which the animal is naturally found, the region in which it is endemic.

oviparous

reproduction in which eggs are released by the female; development of offspring occurs outside the mother's body.

pet trade

the business of buying and selling animals for people to keep in their homes as pets.

polygynandrous

the kind of polygamy in which a female pairs with several males, each of which also pairs with several different females.

riparian

Referring to something living or located adjacent to a waterbody (usually, but not always, a river or stream).

seasonal breeding

breeding is confined to a particular season

sedentary

remains in the same area

sexual

reproduction that includes combining the genetic contribution of two individuals, a male and a female

solitary

lives alone

tactile

uses touch to communicate

temperate

that region of the Earth between 23.5 degrees North and 60 degrees North (between the Tropic of Cancer and the Arctic Circle) and between 23.5 degrees South and 60 degrees South (between the Tropic of Capricorn and the Antarctic Circle).

terrestrial

Living on the ground.

vibrations

movements of a hard surface that are produced by animals as signals to others

visual

uses sight to communicate

Ref­er­ences

Brower, A., M. Cran­field. 2001. Cryp­tosporid­ium sp.-As­so­ci­ated En­teri­tis with­out Gas­tri­tis in Rough Green Snakes. Jour­nal of Zoo and Wildlife Med­i­cine, Vol. 32, No. 1: 101-105.

Cooper, W. 2007. El­e­vated tongue-flick­ing rate to cricket sur­face chem­i­cals by the arthro­po­di­v­o­rous rough green snake Opheodrys aes­tivus. AM­PHIBIA-REP­TILIA, Vol­ume: 28 Issue: 3: 413-417.

Gold­smith, S. 1988. Courtship Be­hav­ior of the Rough Green Snake, Opheodrys aes­tivus (Col­u­bri­dae: Ser­pentes). The South­west­ern Nat­u­ral­ist, Vol. 33, No. 4: 473-477.

Gold­smith, S. 1984. As­pects of the Nat­ural His­tory of the Rough Green Snake, Opheodrys aes­tivus (Col­u­bri­dae). The South­west­ern Nat­u­ral­ist, Vol. 29, No. 4: 445-452.

Gold­smith, S. 1986. Feed­ing Be­hav­ior of an Ar­bo­real, In­sec­tiv­o­rous Snake (Opheodrys aes­tivus) (Col­u­bri­dae). The South­west­ern Nat­u­ral­ist, Vol. 31, No. 2: 246-249.

Gray, B. 2005. The Ser­pent's Cast - A Guide to the Iden­ti­fi­ca­tion of Shed Skins from Snakes of the North­east and Mid-At­lantic States. Lans­ing, Michi­gan: ECO Her­peto­log­i­cal Pub­lish­ing & Dis­tri­b­u­tion.

Mitchell, J. 1994. The Rep­tiles of Vir­ginia. Wash­ing­ton and Lon­don: Smith­son­ian In­sti­tu­tion Press.

Palmer, W., A. Braswell. 1976. Com­mu­nal Egg Lay­ing and Hatch­lings of the Rough Green Snake, Opheodrys aes­tivus. Jour­nal of Her­petol­ogy, Vol. 10, No. 3: 257-259.

Plum­mer, M. 1990. Nest­ing Move­ments, Nest­ing Be­hav­ior, and Nest Sites of Green Snakes (Opheodrys aes­tivus) Re­vealed by Ra­dioteleme­try. Her­peto­log­ica, Vol. 46, No. 2: 190-195.

Plum­mer, M. 1983. An­nual Vari­a­tion in Stored Lipids and Re­pro­duc­tion in Green Snakes (Opheodrys aes­tivus). Copeia, Vol. 1983, No. 3: 741-745.

Plum­mer, M. 1985. De­mog­ra­phy of Green Snakes (Opheodrys aes­tivus). Her­peto­log­ica, Vol. 41, No. 4: 373-381.

Plum­mer, M. 1987. Ge­o­graphic Vari­a­tion in Body Size of Green Snakes (Opheodrys aes­tivus). Copeia, Vol. 1987, No. 2: 483-485.

Plum­mer, M. 1985. Growth and Ma­tu­rity in Green Snakes (Opheodrys aes­tivus). Her­petolig­ica, 41: 28-33.

Plum­mer, M. 1981. Habi­tat Uti­liza­tion, Diet and Move­ments of a Tem­per­ate Ar­bo­real Snake (Opheodrys aes­tivus). Jour­nal of Her­petol­ogy, Vol. 15, No. 4: 425-432.

Plum­mer, M. 1990. High Pre­da­tion on Green Snakes, Opheodrys aes­tivus. Jour­nal of Her­petol­ogy, Vol. 24, No. 3: 327-328.

Plum­mer, M. 1997. Pop­u­la­tion Ecol­ogy of Green Snakes (Opheodrys aes­tivus) Re­vis­ited. Her­peto­log­i­cal Mono­graphs, Vol. 11: 102-123.

Plum­mer, M. 1997. Speed and En­durance of Gravid and Non­gravid Green Snakes, Opheodrys aes­tivus. Copeia, Vol. 1997, No. 1: 191-194.

Plum­mer, M. 1993. Ther­mal Ecol­ogy of Ar­bo­real Green Snakes (Opheodrys aes­tivus). Jour­nal of Her­petol­ogy, Vol. 27, No. 3: 254-260.

Plum­mer, M., H. Snell. 1988. Nest Site Se­lec­tion and Water Re­la­tions of Eggs in the Snake, Opheodrys aes­tivus. Copeia, Vol. 1988, No. 1: 58-64.

Rich­mond, N. 1956. Au­tumn Mat­ing of the Rough Green Snake. Her­peto­log­ica, Vol. 12, No. 4: 325.

Rich­mond, N. 1952. Opheodrys aes­tivus in Aquatic Habi­tats in Vir­ginia. Her­peto­log­ica, Vol. 8, No. 2: 38.

Tin­kle, D. 1960. A Pop­u­la­tion of Opheodrys aes­tivus (Rep­tilia: Squa­mata). Copeia, Vol. 1960, No. 1: 29-34.