Pseudacris cadaverinaCalifornia Treefrog

Ge­o­graphic Range

Cal­i­for­nia tree frogs, also known as Cal­i­for­nia cho­rus frogs (Pseudacris ca­dav­e­rina), are na­tive to North Amer­i­can re­gions. They are found along the coastal parts of South­ern Cal­i­for­nia in the U.S. and Baja Cal­i­for­nia Norte in Mex­ico (Steb­bins and McGin­nis, 2012). Cal­i­for­nia tree frogs can be found in nu­mer­ous coun­ties in South­ern Cal­i­for­nia in­clud­ing: San Luis Obispo to Joshua Tree Na­tional For­est, San Diego, and Gran­ite Moun­tain Pre­serves (Ervin, 2020). (Ervin, 2020; Steb­bins and McGin­nis, 2012)

Habi­tat

Cal­i­for­nia tree frogs are found within the coastal sage and streams of South­ern Cal­i­for­nia and Baja, Mex­ico; these areas range from 0 to 2,290 m above sea level (Steb­bins and McGin­nis, 2012). Adult Cal­i­for­nia tree frogs have been found to pop­u­late a wide range of habi­tats, such as canyon, desert, and coastal streams up into moun­tain stream chan­nels. Al­though they pre­fer to live alone, they have been ob­served co­hab­it­ing streams with fish that eat in­ver­te­brates (Ervin, 2020).

Dur­ing they day, Cal­i­for­nia tree frogs often seek shel­ter in small voids of boul­ders near the wa­ter­line (Ervin, 2020). While these boul­ders are in di­rect sun­light, Cal­i­for­nia tree frogs se­crete a mu­cous film to pre­vent their ep­ithe­lium lay­ers from dry­ing out via evap­o­ra­tion. They are not ac­tive year-round; how­ever, this species un­der­goes aes­ti­va­tion dur­ing pe­ri­ods of ex­treme heat or cold (Al­varez and Con­tr­eras, 2016). As adults, Cal­i­for­nia tree frogs do not spend a large amount of time in the water; how­ever, dur­ing breed­ing sea­son they have been ob­served sit­ting in clean rocky washes with calm pools (Ervin, 2020). Once their eggs are laid and hatched, ju­ve­niles re­main in their breed­ing pools, in areas be­tween small boul­ders and around the bases of an­nual plants. They live in their breed­ing pools until com­plete meta­mor­pho­sis oc­curs (Ervin, 2020). (Al­varez and Con­tr­eras, 2016; Ervin, 2020; Steb­bins and McGin­nis, 2012)

  • Aquatic Biomes
  • lakes and ponds
  • rivers and streams
  • temporary pools
  • Range elevation
    0 to 2,290 m
    0.00 to ft

Phys­i­cal De­scrip­tion

Cal­i­for­nia tree frog tad­poles grow up to 3.7 cm long and have flat­tened bod­ies (Steb­bins and McGin­nis, 2012). They can be dis­tin­guished from sym­patric Baja Cal­i­for­nia tree frogs (Pseudacris hypochon­dri­aca) by their eyes, which are lo­cated within the out­lines of their heads. Al­ter­na­tively, Baja Cal­i­for­nia tree frogs have their eyes on the outer edges of their eyes (Ervin, 2020). Adult Cal­i­for­nia tree frogs have snout-vent lengths (SVL) rang­ing from 2.5 to 5.1 cm long (Steb­bins and McGin­nis, 2012). Their toe pads are char­ac­ter­ized as large in width and short­ened, with web­bing from me­dial to lat­eral toes. They have rough skin with a wide range of color pat­terns that con­sist of gray or light brown skin with small dark brown spots. The ab­domens of Cal­i­for­nia tree frogs ap­pear white, with yel­low­ish limbs and groins (Steb­bins and McGin­nis, 2012). Males can be dis­tin­guished from fe­males by a dusky yel­low color on their necks (Ervin, 2020). Cal­i­for­nia tree frogs can be dis­tin­guished from Baja Cal­i­for­nia tree frogs (Pseudacris hypochon­dri­aca) by the lack of stripes through each eye (Steb­bins and McGin­nis, 2012). (Ervin, 2020; Steb­bins and McGin­nis, 2012)

  • Sexual Dimorphism
  • sexes colored or patterned differently
  • Range length
    2.5 to 5.1 cm
    0.98 to 2.01 in

De­vel­op­ment

The breed­ing sea­son of Cal­i­for­nia tree frogs be­gins in early Feb­ru­ary, after win­ter rains de­cline. Ma­ture males uti­lize mat­ing calls to at­tract ma­ture fe­males into breed­ing ponds and other aquatic areas. Male mat­ing calls are re­peated sounds of quick, deep, and loud duck-like quacks (Cocroft, 1995). Mat­ing and spawn­ing sea­son hap­pens from Feb­ru­ary to early Oc­to­ber (Steb­bins and McGin­nis, 2012). Clutch sizes are un­known; how­ever, in­di­vid­ual eggs are en­cased in a gelati­nous ad­he­sive en­ve­lope. Eggs are typ­i­cally laid in sin­gle strands that end up merg­ing into clumps (Ervin, 2020). The ad­he­sive prop­erty of eggs al­lows for at­tach­ment to sub­merged leaves and de­bris sur­rounded by boul­ders and rocks, which are found in still or slow-mov­ing pools of water (Ervin, 2020). The sub­mer­sion of eggs al­lows for pro­tec­tion against harm­ful UV rays.

Once lar­vae hatch, com­plete meta­mor­pho­sis in lar­vae can be seen after 40 to 75 days (Steb­bins and McGin­nis, 2012). In Cal­i­for­nia, Cal­i­for­nia tree frogs un­dergo meta­mor­pho­sis from June through Au­gust (Ervin, 2020). Ju­ve­nile frogs com­monly re­main near their natal pools for a short pe­riod after meta­mor­pho­sis; how­ever, some im­me­di­ately begin to move into the sur­round­ing habi­tat. Ju­ve­nile Cal­i­for­nia tree frogs reach sex­ual ma­tu­rity at around two years old (Ervin, 2020). (Cocroft and Ryan, 1995; Ervin, 2020; Steb­bins and McGin­nis, 2012)

Re­pro­duc­tion

When mat­ing, Cal­i­for­nia tree frogs pair in in­guinal am­plexus. This means that males climb onto the backs of fe­males and grip their hips tightly. Fe­males de­posit their eggs into breed­ing ponds for ex­ter­nal fer­til­iza­tion by males (Ervin, 2020). The num­ber of mates each sex has in one breed­ing sea­son or life time is un­known.

  • Key Reproductive Features
  • gonochoric/gonochoristic/dioecious (sexes separate)
  • Average age at sexual or reproductive maturity (female)
    2 years
  • Average age at sexual or reproductive maturity (male)
    2 years

After spawn­ing, both male and fe­male tree frogs leave the breed­ing ponds, im­ply­ing lit­tle-to-no parental care (Ervin, 2020).

  • Parental Investment
  • no parental involvement

Lifes­pan/Longevity

Cal­i­for­nia tree frogs reach ma­tu­rity at around 2 years of age. After this point, their longevity is un­known (Ervin, 2020). How­ever, within the same genus, it is known that Pa­cific tree frogs (Pseudacris regilla) can live up to 8 years in cap­tiv­ity (Croft, 1994). (Cocroft, 1994; Ervin, 2020)

Be­hav­ior

Cal­i­for­nia tree frogs are not seen often, due to their noc­tur­nal ten­den­cies (Steb­bins and McGin­nis, 2012). Dur­ing spring and sum­mer days, Cal­i­for­nia tree frogs are known to seek shel­ter in the shaded crevices of rocks and boul­ders, along pools of water (Ervin, 2020). Dur­ing the fall and win­ter, Cal­i­for­nia tree frogs move to higher el­e­vated crevices to avoid heavy rain­fall drainage (Ervin, 2020).

Ma­ture Cal­i­for­nia tree frogs are rarely seen in the water un­less they are breed­ing or avoid­ing pre­da­tion. Even in these cases, they re­turn back to land shortly after. Cal­i­for­nia tree frogs un­dergo a state of tor­por from De­cem­ber to March, as well as ex­treme hot or cold pe­ri­ods dur­ing the rest of the year (Ervin, 2020). Both adults and tad­poles have cryp­tic col­oration to avoid preda­tors (Steb­bins and McGin­nis, 2012).

Males uti­lize vo­cal­iza­tions not only for mat­ing, but also as warn­ing calls to in­tim­i­date com­pet­ing males (Cocroft and Ryan, 1995). Males often show ag­gres­sive and ter­ri­to­r­ial be­hav­iors to­wards the same sex through com­bat and threat­en­ing vo­cal­iza­tions (Steb­bins and McGin­nis, 2012). (Cocroft and Ryan, 1995; Ervin, 2020; Steb­bins and McGin­nis, 2012)

Home Range

Lit­tle is known about the home range of Cal­i­for­nia tree frogs.

Com­mu­ni­ca­tion and Per­cep­tion

Cal­i­for­nia tree frogs uti­lize vo­cal­iza­tion to com­mu­ni­cate dur­ing mat­ing and com­pe­ti­tion. Dur­ing the breed­ing sea­son, male Cal­i­for­nia tree frogs use ad­ver­tise­ment calls to at­tract fe­males into breed­ing ponds. This mat­ing call is a re­peated pat­tern of fast, loud, low-pitched quack­ing sounds (Cocroft and Ryan, 1995). Mat­ing calls sound dif­fer­ent from the warn­ing calls that males use to pro­tect their ter­ri­tory. These warn­ing calls have been char­ac­ter­ized to have a greater in­ten­sity in pitch than mat­ing calls (Ervin, 2020). It is com­mon for Anu­rans (order Anura) to use binoc­u­lar depth per­cep­tion to lo­cate and de­ter­mine dis­tances from their prey (Ewert, 2001). (Cocroft and Ryan, 1995; Ervin, 2020; Ewert, et al., 2001)

Food Habits

Cal­i­for­nia tree frog tad­poles are known to be gen­er­al­ists, with a diet con­sist­ing of plant ma­te­r­ial, pe­ri­phy­ton from algal mats, and or­ganic de­tri­tus found in their natal ponds (Ervin, 2020). As adults, Cal­i­for­nia tree frogs feed on a va­ri­ety of in­ver­te­brate species in­clud­ing cen­tipedes, spi­ders, grasshop­pers, ants, bee­tles, moths, sow bugs, true bugs, and lacewings (Cun­ning­ham, 1964). Like all Anu­rans, Cal­i­for­nia tree frogs use a spe­cial­ized tongue and sticky saliva to catch and bring prey into their mouths. (Cun­ning­ham, 1964; Ervin, 2020)

  • Animal Foods
  • insects

Pre­da­tion

In stream pools, Cal­i­for­nia tree frogs are highly sus­cep­ti­ble to pre­da­tion by rain­bow trout (On­corhynchus mykiss) and aquatic two-striped garter snakes (Thamnophis ham­mondii) (Ervin, 2020). Two-striped garter snakes have also been ob­served eat­ing adult tree frogs due to their shared ge­o­graphic habi­tat range (Ervin, 2020). Adult Cal­i­for­nia tree frogs are often preyed upon by in­va­sive species such as green sun­fish (Lep­omis cyanel­lus) that were in­tro­duced to south­ern Cal­i­for­nia drainage areas (Ervin, 2020).

Both Cal­i­for­nia tree frog tad­poles and adults use cryp­tic col­oration as an anti-preda­tor mech­a­nism. Cal­i­for­nia tree frog lar­vae use vari­a­tions of brown with gold spots to cam­ou­flage with the sand and sub­strates in their natal ponds (Steb­bins and McGin­nis, 2012). As adults, Cal­i­for­nia tree frogs have dor­sal color pat­terns that re­sem­ble rocks and boul­ders. Cal­i­for­nia tree frogs re­main ex­tremely still when preda­tors ap­proach to avoid de­tec­tion; how­ever, they can rapidly jump into nearby streams if at­tacked while they are perch­ing (Cun­ning­ham, 1964). (Cun­ning­ham, 1964; Ervin, 2020; Steb­bins and McGin­nis, 2012)

  • Anti-predator Adaptations
  • cryptic

Ecosys­tem Roles

Cal­i­for­nia tree frogs play an im­por­tant role in their ecosys­tem by con­trol­ling the pop­u­la­tions of in­sects they con­sume. Tad­poles are a vital food source to rain­bow trout (On­corhynchus mykiss) and adults serve as food for two-striped garter snakes (Thamnophis ham­mondii).

Cal­i­for­nia tree frogs have been ob­served to host par­a­sites, such as lar­val chig­gers (Trom­bi­cul­i­dae) em­bed­ded in their skin. In ad­di­tion, Cal­i­for­nia tree frogs have been seen host­ing nu­mer­ous par­a­sitic species of trema­todes and two par­a­sitic species of ne­ma­todes: (Rhab­dias ranae) and Physa­loptera sp. (Ervin, 2020). (Ervin, 2020)

Com­men­sal/Par­a­sitic Species
  • Trom­bi­cul­i­dae

Eco­nomic Im­por­tance for Hu­mans: Pos­i­tive

Cal­i­for­nia tree frogs act as nat­ural pest con­trol for human pop­u­la­tions by main­tain­ing in­sect pop­u­la­tions.

  • Positive Impacts
  • controls pest population

Eco­nomic Im­por­tance for Hu­mans: Neg­a­tive

Since Cal­i­for­nia tree frogs are not an in­va­sive species and do not pos­sess poi­son glands, they are not known to cause any harm to hu­mans or their prop­erty.

Con­ser­va­tion Sta­tus

Ac­cord­ing to the IUCN Red List, Cal­i­for­nia tree frogs are of least con­cern and have sta­ble pop­u­la­tions (Ham­mer­son and San­tos-Bar­rera, 2004). How­ever, threats of urban and com­mer­cial de­vel­op­ment on their pop­u­la­tions is still being in­ves­ti­gated (Ham­mer­son and San­tos-Bar­rera, 2004). In ad­di­tion, ef­fects of the in­tro­duc­tion of non-na­tive preda­tory fish species on Cal­i­for­nia tree frogs are still un­known (Ervin, 2020). (Ervin, 2020; Ham­mer­son and San­tos-Bar­rera, 2004)

Other Com­ments

Adult Cal­i­for­nia tree frogs and Pa­cific tree frogs (Pseudacris regilla) have been re­ported to nat­u­rally hy­bridize to pro­duce vi­able off­spring (Steb­bins and McGin­nis, 2012). How­ever, at­tempts to mate these two species in a lab set­ting has been un­suc­cess­ful, pro­duc­ing in­vi­able off­spring (Ervin, 2020). (Ervin, 2020; Steb­bins and McGin­nis, 2012)

Con­trib­u­tors

Selina Mar­tinez (au­thor), Cal­i­for­nia State Uni­ver­sity, San Mar­cos, Tracey Brown (ed­i­tor), Cal­i­for­nia State Uni­ver­sity, San Mar­cos, Galen Bur­rell (ed­i­tor), Spe­cial Pro­jects.

Glossary

Neotropical

living in the southern part of the New World. In other words, Central and South America.

World Map

acoustic

uses sound to communicate

bilateral symmetry

having body symmetry such that the animal can be divided in one plane into two mirror-image halves. Animals with bilateral symmetry have dorsal and ventral sides, as well as anterior and posterior ends. Synapomorphy of the Bilateria.

carnivore

an animal that mainly eats meat

chaparral

Found in coastal areas between 30 and 40 degrees latitude, in areas with a Mediterranean climate. Vegetation is dominated by stands of dense, spiny shrubs with tough (hard or waxy) evergreen leaves. May be maintained by periodic fire. In South America it includes the scrub ecotone between forest and paramo.

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.

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.

insectivore

An animal that eats mainly insects or spiders.

metamorphosis

A large change in the shape or structure of an animal that happens as the animal grows. In insects, "incomplete metamorphosis" is when young animals are similar to adults and change gradually into the adult form, and "complete metamorphosis" is when there is a profound change between larval and adult forms. Butterflies have complete metamorphosis, grasshoppers have incomplete metamorphosis.

motile

having the capacity to move from one place to another.

mountains

This terrestrial biome includes summits of high mountains, either without vegetation or covered by low, tundra-like vegetation.

native range

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

nocturnal

active during the night

phytoplankton

photosynthetic or plant constituent of plankton; mainly unicellular algae. (Compare to zooplankton.)

planktivore

an animal that mainly eats plankton

suburban

living in residential areas on the outskirts of large cities or towns.

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.

territorial

defends an area within the home range, occupied by a single animals or group of animals of the same species and held through overt defense, display, or advertisement

visual

uses sight to communicate

Ref­er­ences

Al­varez, C., H. Con­tr­eras. 2016. The ef­fect of de­hy­dra­tion on the meta­bolic rate and lo­co­mo­tor per­for­mance of two species of tree frogs found in South­ern Cal­i­for­nia (Pseudacris regilla and P. ca­dav­e­rina). FASEB JOUR­NAL, 30: 1.

Cocroft, R. 1994. A Cladis­tic Analy­sis of Cho­rus Frog Phy­logeny (Hyl­i­dae: Pseudacris). Her­peto­log­ica, 50.4: 420-437. Ac­cessed Feb­ru­ary 18, 2020 at https://​www.​jstor.​org/​stable/​3892719.

Cocroft, R., M. Ryan. 1995. Pat­terns of ad­ver­tise­ment call evo­lu­tion in toads and cho­rus frogs. The As­so­ci­a­tion for the Study of An­i­mal Be­hav­iour, 49/2: 283-303. Ac­cessed Feb­ru­ary 18, 2020 at https://​doi.​org/​10.​1006/​anbe.​1995.​0043.

Cun­ning­ham, J. 1964. Ob­ser­va­tions on the ecol­ogy of the canyon tree frog, Hyla cal­i­for­niae. Her­peto­log­ica, 20: 55-61.

Ervin, E. 2020. "Hyli­ola ca­dav­e­rina" (On-line). Am­phib­i­aWeb. Ac­cessed March 10, 2020 at http://​amphibiaweb.​org.

Ewert, J., H. Buxbaum-Con­radi, F. Dreisvogt, M. Glagow, C. Merkel-Harff, A. Rottgen, E. Schurg-Pfeif­fer, W. Schwip­pert. 2001. Neural Mod­u­la­tion of Vi­suo­mo­tor Func­tions Un­der­ly­ing Prey-Catch­ing Be­hav­iour in Anu­rans: Per­cep­tion, At­ten­tion, Motor Per­for­mance, Learn­ing. El­se­vier, 417: 61.

Ham­mer­son, G., G. San­tos-Bar­rera. 2004. "Pseudacris ca­dav­e­rina" (On-line). The IUCN Red List of Threat­ened Species. Ac­cessed Feb­ru­ary 18, 2020 at https://​dx.​doi.​org/​10.​2305/​IUCN.​UK.​2004.​RLTS.​T55890A11374045.​en.​.

Steb­bins, R., S. McGin­nis. 2012. Field Guide to Am­phib­ians and Rep­tiles of Cal­i­for­nia. Berke­ley and Los An­ge­les, Cal­i­for­nia: Cal­i­for­nia Nat­ural His­tory Guides.