Opheodrys vernalisSmooth Green Snake

Ge­o­graphic Range

Smooth green snakes (Opheodrys ver­nalis) live in the north­east­ern and Mid­west­ern United States, as well as south­ern Canada, in­clud­ing south­ern Que­bec, On­tario, Man­i­toba, as far west as Saskatchewan. The largest con­tin­u­ous por­tion of their range stretches from Maine west­ward to North Dakota, with dis­junct pop­u­la­tions in the Mid­west­ern United States. There are pop­u­la­tions as far south as the south­ern coast of Texas. Their ge­o­graphic range also in­cludes North Car­olina, Kansas, Iowa, Illi­nois, Ten­nessee, Mis­souri, Mis­sis­sippi, and west­ern Vir­ginia. (Gilbart, 2012; Grob­man, 1992; Mitchell, 1974; Stu­art, et al., 2014)

Habi­tat

Smooth green snakes are found in grassy, open areas, such as mead­ows, bogs, and open woods. The areas they in­habit typ­i­cally in­clude wet­lands or open water. Smooth green snakes are pri­mar­ily ter­res­trial, but they may also hang in low branches. Dur­ing the day, they can be found bask­ing on boul­ders or logs. (Gilbart, 2012; Grob­man, 1941; Grob­man, 1992; Mitchell, 1974; Mitchell, 2006; Stu­art, et al., 2014)

  • Aquatic Biomes
  • lakes and ponds

Phys­i­cal De­scrip­tion

Smooth green snakes have smooth, bright green dor­sal scales and white or yel­low ven­tral scales. Their col­oration helps them cam­ou­flage in grass or on low branches. Their dor­sal scales are arranged in 15 rows with api­cal pits close to the cen­ter of each scale. Ju­ve­niles mea­sure 8.3 to 16.5 cm upon hatch­ing. Their col­or­ing is duller than adults and tends to range from olive-green to bluish grey.

Adult smooth green snakes mea­sure 30 to 50 cm and weigh 15.3 to 19.5 g. Their tails make up nearly half of their total body length. Their ver­te­bral scales range in width from 0.50 to 0.71 mm, with an av­er­age of 0.62 mm. Smooth green snakes have heads rang­ing from 0.74 to 0.83 mm in width.

Smooth green snakes ex­hibit sub­tle sex­ual di­mor­phism. Fe­males tend to be wider than males and males have longer, more slen­der tails. (Gray, 2005; Grob­man, 1941; Grob­man, 1992; Mitchell, 1974; Mitchell, 2006; Stu­art, et al., 2014)

  • Sexual Dimorphism
  • female larger
  • sexes shaped differently
  • Range mass
    15.3 to 19.5 g
    0.54 to 0.69 oz
  • Average mass
    17 g
    0.60 oz
  • Range length
    30 to 66 cm
    11.81 to 25.98 in
  • Average length
    50 cm
    19.69 in

De­vel­op­ment

Smooth green snakes hatch from eggs, which in­cu­bate for up to 30 days and hatch in late April to Sep­tem­ber. Hatch­lings are 8 to 16 cm long and weigh 1.1 g at birth.

Ju­ve­nile smooth green snakes are not as brightly col­ored as adults and are around half the length. Ju­ve­niles are gray­ish brown in color, which helps them cam­ou­flage with their en­vi­ron­ment. Adults reach 30 to 66 cm in length and reach sex­ual ma­tu­rity at around 2 years old. Smooth green snakes shed their scales as they grow, grad­u­ally de­vel­op­ing their adult col­oration with each shed. They ex­hibit in­de­ter­mi­nate growth, mean­ing they do not stop grow­ing through­out their lifes­pans.

Smooth green snakes ex­hibit tem­per­a­ture-de­pen­dent sex de­ter­mi­na­tion. For eggs that de­velop at tem­per­a­tures above 28 °C, hatch­lings are more likely to be fe­male. For eggs that de­velop below 28 °C, hatch­lings are more likely to be males. Ini­tial in­cu­ba­tion tem­per­a­ture is an im­por­tant de­ter­mi­nant of sex. For ex­am­ple, if the ini­tial in­cu­ba­tion tem­per­a­ture is below 28 °C and changes to a higher tem­per­a­ture later dur­ing in­cu­ba­tion, the re­sult­ing hatch­lings will be males. Typ­i­cally, all of the hatch­lings from a sin­gle clutch of eggs will be one sex. Clutches of eggs typ­i­cally fail when tem­per­a­tures vary more than 10 °C above or below 28 °C. (Aldridge and Sem­l­itsch, 1992; Mitchell, 1974; Plum­mer, 1985a; Plum­mer, 1985b; Sac­er­dote-Ve­lat, et al., 2013)

Re­pro­duc­tion

Smooth green snakes are polyg­y­nan­drous. Fe­males re­lease pheromones to sig­nal their sex­ual ma­tu­rity. Males de­tect the pheromones that fe­males re­lease and con­gre­gate in large num­bers to mate. Males crawl over and bump into fe­males be­fore mat­ing. When fe­males are ready to mate, they lift their tail and ex­pose their cloaca. Dur­ing cop­u­la­tion, males in­sert their hemipenes into the cloaca of their mate and re­lease sperm. (Grob­man, 1992; Naul­leau and Bon­net, 1995; Plum­mer, 1985a; Shine, 2003)

Smooth green snakes re­pro­duce sex­u­ally. They breed once a year, and fe­males ges­tate eggs for an av­er­age of 50 days, lay­ing them be­tween June and Sep­tem­ber. Smooth green snakes lay 3 to 13 eggs per clutch, and eggs in­cu­bate for 4 to 30 days, de­pend­ing on the tem­per­a­ture, with an av­er­age of 27 days. Higher in­cu­ba­tion tem­per­a­tures re­sult in shorter in­cu­ba­tion pe­ri­ods be­fore eggs hatch.

Fe­male smooth green snakes lay their eggs in warm, pro­tected sites, such as mounds or bur­rows with rot­ting veg­e­ta­tion, or un­der­neath fallen logs. Smooth green snakes are sec­ondary cav­ity nesters, choos­ing ex­ist­ing bur­rows that have been va­cated rather than con­struct­ing their own.

Both male and fe­male smooth green snakes reach re­pro­duc­tive ma­tu­rity at around two years old. (Aldridge and Sem­l­itsch, 1992; Grob­man, 1992; Naul­leau and Bon­net, 1995; Plum­mer, 1985a; Seigel and Collins, 2001)

  • Breeding interval
    Smooth green snakes breed once each year
  • Breeding season
    Females lay eggs from June to September, young hatch in August or September
  • Range number of offspring
    3 to 13
  • Average gestation period
    50 days
  • Average time to independence
    0 minutes
  • Average age at sexual or reproductive maturity (female)
    2 years
  • Average age at sexual or reproductive maturity (male)
    2 years

Smooth green snakes ex­hibit lim­ited parental in­vest­ment. Young are im­me­di­ately in­de­pen­dent upon hatch­ing. Fe­males lay their eggs in com­mu­nal nest­ing sites, typ­i­cally in areas that are pro­tected and en­cour­age egg de­vel­op­ment. Males ex­hibit no parental in­vest­ment be­yond the act of mat­ing. (Aldridge and Sem­l­itsch, 1992; Grob­man, 1992; Naul­leau and Bon­net, 1995; Plum­mer, 1985a; Sac­er­dote-Ve­lat, et al., 2013; Shine, 2003)

  • Parental Investment
  • pre-hatching/birth
    • provisioning
      • female
    • protecting
      • female

Lifes­pan/Longevity

Smooth green snakes live an av­er­age of 5 years in the wild, with a max­i­mum recorded lifes­pan of 8 years. In cap­tiv­ity, smooth green snakes live 6 years on av­er­age. Mor­tal­ity in the wild is most often at­trib­uted to pre­da­tion or en­vi­ron­men­tal fac­tors such as flood­ing. (Plum­mer, 1985a; Plum­mer, 1985b; Plum­mer, 1997a; Plum­mer, 1997b; Sac­er­dote-Ve­lat, et al., 2013)

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

Be­hav­ior

Smooth green snakes are mostly soli­tary, al­though large groups form dur­ing breed­ing and nest­ing sea­son and dur­ing win­ter, when in­di­vid­u­als bru­mate to­gether. Smooth green snakes stay in the same gen­eral area through­out their life, but move around to find prey, mates, and shel­ter.

Smooth green snakes are di­ur­nal and ac­tive from April to Oc­to­ber. They are sec­ondary cav­ity nesters, mean­ing they take shel­ter in aban­doned mounds or bur­rows cre­ated by other an­i­mals such as ro­dents.

Smooth green snakes are docile. In cap­tiv­ity, they are not ag­gres­sive to other an­i­mals that do not threaten them. How­ever, when pro­voked, smooth green snakes often re­lease a foul-smelling sub­stance from their anal glands, which can deter po­ten­tial preda­tors.

Smooth green snakes mate be­tween late April and Sep­tem­ber. They are promis­cu­ous, mean­ing that males and fe­males both have mul­ti­ple mates within a sin­gle breed­ing pe­riod. (Grob­man, 1992; Plum­mer, 1997a; Plum­mer, 1997b)

Home Range

Smooth green snakes have an av­er­age home range of 25 km^2. They are not known to ac­tively de­fend a ter­ri­tory.

Com­mu­ni­ca­tion and Per­cep­tion

Smooth green snakes have forked tongues, which they use to de­tect chem­i­cal sig­nals in their en­vi­ron­ment. Smooth green snakes rely on their vomeronasal sys­tem, which di­rects chem­i­cals from their tongue and nose to their Ja­cob­son’s organ. Ja­cob­son’s or­gans help smooth green snakes de­ter­mine the di­rec­tion­al­ity of chem­i­cal sig­nals, which al­lows them to ef­fec­tively track prey, find mates, and avoid preda­tors.

Smooth green snakes also use tac­tile and acoustic meth­ods of com­mu­ni­cat­ing and per­ceiv­ing their en­vi­ron­ment. (Filo­ramo and Schwenk, 2009; Grob­man, 1941; Mitchell, 1974; Seigel and Collins, 2001; Shine, 2003; Stu­art, et al., 2014)

Food Habits

Smooth green snakes are op­por­tunis­tic preda­tors. Around 85% of their diet con­sists of in­sects, such as ants (fam­ily Formi­ci­dae), moths (order Lep­i­doptera), cen­tipedes (class Chilopoda), spi­ders (order Araneae), slugs (class Gas­tropoda), and ter­res­trial worms (phy­lum An­nel­ida). Smooth green snakes use their vomeronasal sys­tems to de­tect chem­i­cals re­leased by prey species. (Mitchell, 1974)

  • Animal Foods
  • insects
  • terrestrial non-insect arthropods
  • mollusks
  • terrestrial worms

Pre­da­tion

Smooth green snakes serve as prey for a va­ri­ety of mam­malian, avian, and rep­til­ian preda­tors. Known mam­malian preda­tors in­clude hu­mans (Homo sapi­ens), black bears (Ursus amer­i­canus), rac­coons (Pro­cyon lotor), red foxes (Vulpes vulpes), and do­mes­tic cats (Felis do­mes­ti­cus). Avian preda­tors in­clude red-tailed hawks (Buteo ja­maicen­sis), great blue herons (Ardea hero­dias), rough-legged hawks (Buteo lago­pus). Larger snakes, such as milk snakes (Lam­pro­peltis tri­an­gu­lum), are also known preda­tors of smooth green snakes.

Smooth green snakes have bright green dor­sal scales, which help them cam­ou­flage in the grass­land and for­est habi­tats where they typ­i­cally live. Smooth green snakes are also small and fast, mak­ing them dif­fi­cult to catch if de­tected. (Aldridge, et al., 1990)

  • Anti-predator Adaptations
  • cryptic

Ecosys­tem Roles

Smooth green snakes serve as prey for mam­mals, birds, and other snake species. They also serve as hosts for par­a­sitic tape­worms (class Ces­toda), par­a­sitic ne­ma­todes (genus Baylisas­caris), and red mites (Der­manys­sus gal­li­nae). (Aldridge, et al., 1990; Grob­man, 1941; Grob­man, 1992; Mitchell, 2006; Red­der, et al., 2006)

Com­men­sal/Par­a­sitic Species

Eco­nomic Im­por­tance for Hu­mans: Pos­i­tive

Smooth green snakes are a part of the in­ter­na­tional pet trade and are oc­ca­sion­ally found in zoos. They also serve as a source of eco­tourism through­out their range. (Aldridge, et al., 1990; Grob­man, 1941; Red­der, et al., 2006; Sac­er­dote-Ve­lat, et al., 2013)

Eco­nomic Im­por­tance for Hu­mans: Neg­a­tive

Smooth green snakes are not ven­omous, but can still bite hu­mans or pets. If left un­treated, their bites can cause in­fec­tions. There are no other known ad­verse ef­fects of smooth green snakes on hu­mans. (Aldridge, et al., 1990; Grob­man, 1941; Red­der, et al., 2006; Stu­art, et al., 2014; Aldridge, et al., 1990; Grob­man, 1941; Red­der, et al., 2006; Stu­art, et al., 2014)

  • Negative Impacts
  • injures humans
    • bites or stings

Con­ser­va­tion Sta­tus

Smooth green snakes are con­sid­ered a species of "least con­cern" on the IUCN Red List. They have no spe­cial sta­tus on other na­tional or in­ter­na­tional con­ser­va­tion lists. How­ever, habi­tat loss due to an­thro­pogenic de­vel­op­ment has neg­a­tively im­pacted pop­u­la­tions of smooth green snakes. In the Rocky Moun­tain re­gion, in­di­vid­u­als are being rein­tro­duced to habi­tats where de­for­esta­tion is not cur­rently a threat. (Aldridge, et al., 1990; Grob­man, 1941; Red­der, et al., 2006; Stu­art, et al., 2014)

Con­trib­u­tors

Lau­ren Mc­Claugh­erty (au­thor), Rad­ford Uni­ver­sity, Karen Pow­ers (ed­i­tor), Rad­ford Uni­ver­sity, April Tin­gle (ed­i­tor), Rad­ford Uni­ver­sity, Emily Clark (ed­i­tor), Rad­ford Uni­ver­sity, Cari Mc­gre­gor (ed­i­tor), Rad­ford Uni­ver­sity, Jacob Vaught (ed­i­tor), Rad­ford Uni­ver­sity, Galen Bur­rell (ed­i­tor), Spe­cial Pro­jects.

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

acoustic

uses sound to communicate

arboreal

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

bog

a wetland area rich in accumulated plant material and with acidic soils surrounding a body of open water. Bogs have a flora dominated by sedges, heaths, and sphagnum.

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.
ecotourism

humans benefit economically by promoting tourism that focuses on the appreciation of natural areas or animals. Ecotourism implies that there are existing programs that profit from the appreciation of natural areas or animals.

ectothermic

animals which must use heat acquired from the environment and behavioral adaptations to regulate body temperature

forest

forest biomes are dominated by trees, otherwise forest biomes can vary widely in amount of precipitation and seasonality.

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.

indeterminate growth

Animals with indeterminate growth continue to grow throughout their lives.

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).

marsh

marshes are wetland areas often dominated by grasses and reeds.

motile

having the capacity to move from one place to another.

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.

pheromones

chemicals released into air or water that are detected by and responded to by other animals of the same species

polygynandrous

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

scrub forest

scrub forests develop in areas that experience dry seasons.

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.

tropical savanna and grassland

A terrestrial biome. Savannas are grasslands with scattered individual trees that do not form a closed canopy. Extensive savannas are found in parts of subtropical and tropical Africa and South America, and in Australia.

savanna

A grassland with scattered trees or scattered clumps of trees, a type of community intermediate between grassland and forest. See also Tropical savanna and grassland biome.

temperate grassland

A terrestrial biome found in temperate latitudes (>23.5° N or S latitude). Vegetation is made up mostly of grasses, the height and species diversity of which depend largely on the amount of moisture available. Fire and grazing are important in the long-term maintenance of grasslands.

vibrations

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

visual

uses sight to communicate

Ref­er­ences

Aldridge, R., J. Green­haw, M. Plum­mer. 1990. The male re­pro­duc­tive cycle of the rough green snake (Opheodrys aes­tivus). Am­phibia-Rep­tilia, 13/3: 165-172.

Aldridge, R., R. Sem­l­itsch. 1992. Fe­male re­pro­duc­tive bi­ol­ogy of the south­east­ern crowned snake (Tan­tilla coro­nata). Am­phibia-Rep­tilia, 13/3: 209-218.

Filo­ramo, N., K. Schwenk. 2009. The mech­a­nism of chem­i­cal de­liv­ery to the vomeronasal or­gans in squa­mate rep­tiles: A com­par­a­tive mor­pho­log­i­cal ap­proach. Jour­nal of Ex­per­i­men­tal Zo­ol­ogy Part B: Mol­e­c­u­lar & De­vel­op­men­tal Evo­lu­tion, 311A/1: 20.

Gilbart, M. 2012. Under Cover: Wildlife of Shrub­lands and Young For­est. Wildlife Man­age­ment In­sti­tute: US Fish & Wildlife Pub­li­ca­tions.

Gray, B. 2005. The Ser­pent's Cast. Lans­ing, Michi­gan: Her­peto­log­i­cal Pub­lish­ing and Dis­tri­b­u­tion.

Grob­man, A. 1941. A Con­tri­bu­tion to the Knowl­edge of Vari­a­tion in Opheodrys ver­nalis (Har­lan), with the De­scrip­tion of a New Sub­species. Uni­ver­sity of Michi­gan: Mis­cel­la­neous Pub­li­ca­tions.

Grob­man, A. 1992. Metamerism in the snake Opheodrys ver­nalis, with a de­scrip­tion of a new sub­species. Jour­nal of Her­petol­ogy, 26/2: 175-186.

Mitchell, J. 1974. The Snakes of Vir­ginia. Uni­ver­sity of Rich­mond: Vir­ginia Wildlife.

Mitchell, J. 2006. Sta­tus of the smooth green snake (Opheodrys ver­nalis) in North Car­olina and Vir­ginia. Ban­is­te­ria, 28: 37-43.

Naul­leau, G., X. Bon­net. 1995. Re­pro­duc­tive ecol­ogy, body fat re­serves and for­ag­ing mode in fe­males of two con­trasted snake species: Vípera aspis (ter­res­trial, vi­vip­a­rous) and Elaphe longíssima (semi-ar­bo­real, oviparous). Am­phibia-Rep­tilia, 16/1: 37-46.

Plum­mer, M. 1985. De­mog­ra­phy of green snakes (Opheodrys aes­tivus). Copeia, 41/4: 373-381.

Plum­mer, M. 1985. Growth and ma­tu­rity in green snakes (Opheodrys aes­tivus). Copeia, 41/1: 28-33.

Plum­mer, M. 1997. Pop­u­la­tion ecol­ogy of green snakes (Opheodrys aes­tivus) re­vis­ited. Her­peto­log­i­cal Mono­graphs, 11/1997: 102-123.

Plum­mer, M. 1997. Speed and en­durance of gravid and non­gravid green snakes, Opheodrys aes­tivus. Copeia, 41/1: 191-194.

Red­der, A., B. Smith, D. Keinath. 2006. "Smooth Green Snake (Opheodrys ver­nalis): A Tech­ni­cal Con­ser­va­tion As­sess­ment" (On-line pdf). So­ci­ety for Con­ser­va­tion Bi­ol­ogy. Ac­cessed March 27, 2015 at http://​www.​fs.​fed.​us/​r2/​projects/​scp/​assessments/​smoothgreensnake.​pdf.

Sac­er­dote-Ve­lat, A., J. Earn­hardt, D. Mulk­erin, D. Boehm, G. Glowacki. 2013. Eval­u­a­tion of head­start­ing and re­lease tech­niques for pop­u­la­tion aug­men­ta­tion and rein­tro­duc­tion of the smooth green snake. An­i­mal Con­ser­va­tion, 17/1: 65-73.

Seigel, R., J. Collins. 2001. Snakes: Ecol­ogy and Be­hav­ior. Cald­well, N.J: Black­burn Press.

Shine, R. 2003. Re­pro­duc­tive strate­gies in snakes. Pro­ceed­ings of the Royal So­ci­ety of Lon­don B, 270/1519: 995-1004.

Stu­art, B., J. Rosado, P. Brinkman. 2014. Al­bert Rogers Cran­dall's smooth green snake (Opheodrys ver­nalis) from North Car­olina. South­east­ern Nat­u­ral­ist, 13/4: 36-43.