Hyperolius viridiflavus

Ge­o­graphic Range

Hy­per­olius virid­i­flavus, or African reed frogs, are a wide­spread species that oc­cupy most suit­able habi­tats (ponds and lakes) through­out north­west­ern Ethiopia, through South­ern Sudan to west­ern Kenya, Rwanda, Uganda, Bu­rundi, north­west­ern Tan­za­nia, north­east­ern De­mo­c­ra­tic Re­pub­lic of Congo, and most likely east­ern Cen­tral African Re­pub­lic. (Schiøtz, et al., 2004)

Habi­tat

Hy­per­olius virid­i­flavus lives in the trop­i­cal African sa­vanna. It is as­so­ci­ated with emerg­ing veg­e­ta­tion in sa­vanna, grass­lands, and at the mar­gins of forests, lakes, rivers, and swamps, where these frogs may live in high den­si­ties. Hy­per­olius virid­i­flavus also lives in areas as­so­ci­ated with hu­mans, like cul­ti­vated land and gar­dens. This species breeds in a va­ri­ety of aquatic habi­tats from very small to large ponds that may be per­ma­nent but are usu­ally tem­po­rary. It ranges from low al­ti­tudes to 2,400 m in Ethiopia. (Schiøtz, et al., 2004; Schiøtz, 1999)

  • Aquatic Biomes
  • lakes and ponds
  • rivers and streams
  • temporary pools
  • Range elevation
    2,400 (high) m
    ft

Phys­i­cal De­scrip­tion

Hy­per­olius virid­i­flavus is a highly vari­able species that ex­hibits con­sid­er­able poly­mor­phism in color pat­tern. Some pop­u­la­tions con­tain dis­tinct morphs while in oth­ers there is gra­da­tion among ex­tremes. It is widely re­garded as a su­per­species with more than fifty sub­species rec­og­nized. The sub­species are di­vided into two sub­groups, par­al­lelus and virid­i­flavus, based on vari­a­tion in ge­o­graphic range and col­oration. There is some con­tro­versy about the tax­on­omy of H. virid­i­flavus that is dis­cussed fur­ther in the other com­ments sec­tion.

Hy­per­olius virid­i­flavus is a small to medium sized frog species with an av­er­age mass of 2 g and body length of 15 to 30 mm, de­pend­ing on the sub­species.

This species ex­hibits sex­ual di­mor­phism with males slightly smaller than fe­males. Fe­males are more col­or­ful than males; their adult pat­tern is re­ferred to as Phase F which is highly vari­able and con­tains sev­eral dis­tinct morphs. Ma­ture males fre­quently re­main in the ju­ve­nile phase (Phase J), which ranges from brown­ish to green with paired light dor­so­lat­eral lines.

Mem­bers of this species have hor­i­zon­tal pupils, ex­ten­sive web­bing of the feet, a brief snout, and a very large, sha­greened, gular flap. They lack an ex­ter­nal metatarsal tu­ber­cle. Males have a large di­lat­able vocal sac. Fe­males have a tran­verse gular flap All sub­species have a sub­der­mal dark bluish lat­eral streak caused by black pig­men­ta­tion of the mus­cu­lus obliquus ab­dom­i­nal mus­cle. This band is some­times dif­fi­cult to see if the sides of the frog are heav­ily pig­mented. The band dif­fers in place­ment be­tween the sexes.

The sub­species have dif­fer­ent col­oration rang­ing from solid light green in the H. virid­i­flavus mwan­zae to light brown in H. virid­i­flavus pan­ther­i­nus to very brightly spot­ted and striped in H. virid­i­flavus tau­nia­tus. The feet are fre­quently brightly col­ored. (Grafe, et al., 1992; Schiøtz, et al., 2004; Schiøtz, 1999)

  • Sexual Dimorphism
  • female larger
  • sexes colored or patterned differently
  • female more colorful
  • Average mass
    2 g
    0.07 oz
  • Range length
    14 to 33 mm
    0.55 to 1.30 in

De­vel­op­ment

Hy­per­olius virid­i­flavus eggs hatch into tad­poles two to five days after lay­ing, de­pend­ing on the tem­per­a­ture of the water. Tad­poles take eight weeks to meta­mor­phose into ju­ve­niles. Ju­ve­niles ma­ture sex­u­ally in three to twelve months de­pend­ing on the cli­mate. Ju­ve­nile H. virid­i­flavus have a dif­fer­ent col­oration than adults, re­ferred to as Phase J, which is light brown to green in color. Sex­u­ally ma­ture males fre­quently main­tain the ju­ve­nile col­oration through­out adult­hood. Phase F, the adult phase, is a highly vari­able color pat­tern with dis­tinct morphs. (Bubac, 2009; Grafe and Lisen­mair, 1989; Schiøtz, 1999)

Re­pro­duc­tion

Hy­per­olius virid­i­flavus breeds dur­ing the wet sea­son. The length of the breed­ing ac­tiv­ity varies among sub­species but typ­i­cally lasts sev­eral months. This species is polyg­y­nan­drous. At the be­gin­ning of the breed­ing sea­son, males mi­grate to bod­ies of water such as shal­low ponds and form call­ing cho­ruses to at­tract mates. Males main­tain an in­di­vid­ual call­ing space through com­bat. Males typ­i­cally call at dusk and ex­pend con­sid­er­able en­ergy try­ing to at­tract a mate. Fe­males H. virid­i­flavus may se­lect larger males as mates. Fe­males ap­proach males and ini­ti­ate am­plexus. Am­plexus is ax­il­lary (the male holds the fe­male around the armpits). The eggs are laid on veg­e­ta­tion under the water in ponds, lakes, and slow-mov­ing streams. Fe­male H. virid­i­flavus pro­duce mul­ti­ple clutches dur­ing the breed­ing sea­son. (Bubac, 2009; Grafe and Lisen­mair, 1989; Grafe, et al., 1992)

Hy­per­olius virid­i­flavus breeds dur­ing the wet sea­son. The length of the breed­ing ac­tiv­ity varies among sub­species but typ­i­cally lasts sev­eral months. Fe­males have mul­ti­ple clutches over the course of the breed­ing sea­son. The av­er­age size of a clutch is 330 eggs. Eggs hatch after 2 to 5 days, and have meta­mor­phosed into ju­ve­niles by 8 weeks of age. Ju­ve­niles of both sexes be­come sex­u­ally ma­ture at 4 to 12 months old.

Hy­per­olius virid­i­flavus has been shown to ex­pe­ri­ence pro­tog­yny, or fe­male to male sex change, in the lab­o­ra­tory. The new males were able to fer­til­ize the eggs of fe­males. This likely oc­curs when the sex ratio within a pop­u­la­tion is heav­ily weighted to­wards males.

Hy­per­olius virid­i­flavus is semel­parous, but may breed mul­ti­ple times in its one breed­ing sea­son. This re­pro­duc­tive strat­egy is largely due to cli­matic fac­tors, as no adults have been doc­u­mented sur­viv­ing the an­nual, harsh dry sea­son. Even in lab­o­ra­tory set­tings, in­di­vid­u­als will senesce shortly after the breed­ing sea­son. (Grafe and Lisen­mair, 1989)

  • Breeding interval
    Female Hyperolius viridiflavus produce a new clutch every 10 to 20 days during the breeding season.
  • Breeding season
    Hyperolius viridiflavus breed during the wet season which typically lasts several months.
  • Range number of offspring
    94 to 800
  • Range time to hatching
    2 to 5 days
  • Range age at sexual or reproductive maturity (female)
    4 to 12 months
  • Range age at sexual or reproductive maturity (male)
    4 to 12 months

Hy­per­olius virid­i­flavus pro­vides no parental in­vest­ment other than yolk and sperm for the eggs. (Bubac, 2009)

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

Lifes­pan/Longevity

Hy­per­olius virid­i­flavus lives in an en­vi­ron­ment with widely fluc­tu­at­ing weather con­di­tions. Shortly after the breed­ing sea­son, these frogs face a se­vere dry sea­son when they must rely on stored water. Adults do not han­dle this water short­age as well as ju­ve­niles. Adults do not gen­er­ally sur­vive the dry sea­son, and in areas with pro­longed dry sea­sons adults are prob­a­bly an­nual. Lin­sen­mair has never found an adult H. virid­i­flavus ni­tidu­lus that has sur­vived the dry sea­son in West Africa. Even under lab­o­ra­tory con­di­tions, adult H. virid­i­flavus senesce quickly after the end of breed­ing ac­tiv­ity. Males also ex­pe­ri­ence high mor­tal­ity be­cause they are highly vocal and are there­fore more sus­cep­ti­ble to pre­da­tion by acousti­cally-hunt­ing preda­tors. (Geise and Lin­sen­mair, 1988; Grafe and Lisen­mair, 1989)

  • Typical lifespan
    Status: wild
    1 (high) years

Be­hav­ior

These frogs uti­lize ex­posed call­ing sites and males ex­hibit ter­ri­to­r­ial be­hav­ior dur­ing the breed­ing sea­son at these sites. In order to main­tain an in­di­vid­ual call­ing site, males en­gage in in­tense and pro­longed com­bat. Dur­ing the dry sea­son, H. virid­i­flavus aes­ti­vates. Ju­ve­niles es­ti­vate on dry veg­e­ta­tion in ex­posed po­si­tions, in­stead of bur­row­ing in the ground. This be­hav­ior is unique among frogs. Only ju­ve­niles are able to sur­vive the dry sea­son; they do so by re­duc­ing me­tab­o­lism and ad­just­ing water econ­omy. Adults are not able to make these changes and gen­er­ally do not sur­vive the dry sea­son. Ju­ve­niles do not move, eat, uri­nate, or defe­cate dur­ing the dry sea­son. Ju­ve­niles must rely on stored water for sev­eral months dur­ing the dry sea­son so they must min­i­mize evap­o­ra­tive water loss. The dor­sal and ven­tral skin of H. virid­i­flavus is dif­fer­en­ti­ated in order to max­i­mize water con­ser­va­tion and up­take. Dur­ing the dry sea­son the skin turns white be­cause of built-up purine crys­tals in the skin. (Geise and Lin­sen­mair, 1988; Grafe and Lisen­mair, 1989)

Home Range

There is no in­for­ma­tion on home range for this species.

Com­mu­ni­ca­tion and Per­cep­tion

Hy­per­olius virid­i­flavus has a melodic call like a xy­lo­phone that is more tonal than that of other species in this genus. Their calls are a char­ac­ter­is­tic part of the African night sounds. Males have an ex­posed call­ing site and form cho­ruses in order to at­tract mates.

Hy­per­olius virid­i­flavus ni­tidu­lus males have two dis­tinct calls, a mat­ing call and a ter­ri­to­r­ial call. The ter­ri­to­r­ial call is longer and deeper than the mat­ing call, and lasts from 0.28 to 0.36 sec­onds and has a fre­quency of 0.98 to 2.6 kHz. The mat­ing call is a short metal­lic click that lasts be­tween 0.10 to 0.24 s and has a fre­quency of 2.04 to 3.43 kHz, de­pend­ing on the size of the frog. Fe­male H. virid­i­flavus can­not make sounds.

Mem­bers of this species use keen vi­sual per­cep­tion in order to cap­ture in­sects. They have bulging eyes and hor­i­zon­tal pupils. (Bubac, 2009; Grafe and Lisen­mair, 1989; Schiøtz, et al., 2004; Schiøtz, 1999)

Food Habits

Hy­per­olius virid­i­flavus are in­sec­ti­vores that feed on many dif­fer­ent types of in­sects in­clud­ing flies in the gen­era Drosophila, Musca, Phormia, Lu­cilia, and Cal­liphora. The free-liv­ing tad­poles of Hy­per­olius virid­i­flavus ni­tidu­lus eat algae. (Bubac, 2009)

  • Animal Foods
  • insects
  • Plant Foods
  • algae

Pre­da­tion

Hy­per­olius virid­i­flavus has a bright warn­ing col­oration that wards off preda­tors. Drag­on­fly lar­vae, bee­tle lar­vae, tur­tles, ray-finned fish and water snakes eat the tad­poles of H. virid­i­flavus. (Bubac, 2009)

Ecosys­tem Roles

Hy­per­olius virid­i­flavus is a preda­tor of in­sects in the African sa­vanna. It is also the prey of sev­eral species of an­i­mals. (Grafe and Lisen­mair, 1989)

Eco­nomic Im­por­tance for Hu­mans: Pos­i­tive

This species is a part of the in­ter­na­tional pet trade al­though not at high lev­els. (Schiøtz, et al., 2004)

Eco­nomic Im­por­tance for Hu­mans: Neg­a­tive

There are no known ad­verse ef­fects of Hy­per­olius virid­i­flavus on hu­mans. How­ever, the Masai of East Africa have a su­per­sti­tion that their cat­tle will die if they eat these frogs be­cause of their bright warn­ing col­oration. (Schiøtz, 1999)

Con­ser­va­tion Sta­tus

Hy­per­olius virid­i­flavus is listed as least con­cern by the In­ter­na­tional Union for Con­ser­va­tion of Na­ture be­cause of its very wide dis­tri­b­u­tion and tol­er­ance of a broad range of habi­tats. It also likely has a large pop­u­la­tion size with no sig­nif­i­cant threats. This species is oc­ca­sion­ally found in the in­ter­na­tional pet trade, but not at a high enough level to pose a threat to it. (Schiøtz, et al., 2004)

Other Com­ments

The tax­on­omy of Hy­per­olius virid­i­flavus is com­plex and has been the sub­ject of much de­bate. Much of the dif­fi­culty has come from the de­pen­dence on dor­sal color pat­terns as tax­o­nomic char­ac­ters. Schiøtz ar­gues that H. virid­i­flavus is a su­per­species with many sub­species that can be di­vided into two sub­groups, par­al­lelus and virid­i­flavus based on col­oration and ge­o­graphic range. Wiec­zorek has bro­ken up the var­i­ous sub­species of H. virid­i­flavus into ten full species based on mi­to­chon­dr­ial DNA. Adult H. virid­i­flavus are unique be­cause they can re­gen­er­ate fully func­tional dig­its after am­pu­ta­tion. (Richards, et al., 1975; Schiøtz, 1975; Wiec­zorek, et al., 2001)

Con­trib­u­tors

Jen­nifer Brady (au­thor), Uni­ver­sity of Michi­gan-Ann Arbor, Phil Myers (ed­i­tor), Uni­ver­sity of Michi­gan-Ann Arbor, Rachelle Ster­ling (ed­i­tor), Spe­cial Pro­jects.

Glossary

Ethiopian

living in sub-Saharan Africa (south of 30 degrees north) and Madagascar.

World Map

acoustic

uses sound to communicate

agricultural

living in landscapes dominated by human agriculture.

aposematic

having coloration that serves a protective function for the animal, usually used to refer to animals with colors that warn predators of their toxicity. For example: animals with bright red or yellow coloration are often toxic or distasteful.

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

choruses

to jointly display, usually with sounds, at the same time as two or more other individuals of the same or different species

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

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

external fertilization

fertilization takes place outside the female's body

fertilization

union of egg and spermatozoan

freshwater

mainly lives in water that is not salty.

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.

insectivore

An animal that eats mainly insects or spiders.

marsh

marshes are wetland areas often dominated by grasses and reeds.

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.

natatorial

specialized for swimming

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.

polymorphic

"many forms." A species is polymorphic if its individuals can be divided into two or more easily recognized groups, based on structure, color, or other similar characteristics. The term only applies when the distinct groups can be found in the same area; graded or clinal variation throughout the range of a species (e.g. a north-to-south decrease in size) is not polymorphism. Polymorphic characteristics may be inherited because the differences have a genetic basis, or they may be the result of environmental influences. We do not consider sexual differences (i.e. sexual dimorphism), seasonal changes (e.g. change in fur color), or age-related changes to be polymorphic. Polymorphism in a local population can be an adaptation to prevent density-dependent predation, where predators preferentially prey on the most common morph.

rainforest

rainforests, both temperate and tropical, are dominated by trees often forming a closed canopy with little light reaching the ground. Epiphytes and climbing plants are also abundant. Precipitation is typically not limiting, but may be somewhat seasonal.

riparian

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

saltatorial

specialized for leaping or bounding locomotion; jumps or hops.

seasonal breeding

breeding is confined to a particular season

sedentary

remains in the same area

semelparous

offspring are all produced in a single group (litter, clutch, etc.), after which the parent usually dies. Semelparous organisms often only live through a single season/year (or other periodic change in conditions) but may live for many seasons. In both cases reproduction occurs as a single investment of energy in offspring, with no future chance for investment in reproduction.

sexual

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

swamp

a wetland area that may be permanently or intermittently covered in water, often dominated by woody vegetation.

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

tropical

the region of the earth that surrounds the equator, from 23.5 degrees north to 23.5 degrees south.

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.

visual

uses sight to communicate

Ref­er­ences

Bubac, C. 2009. "Hy­per­olius ni­tidu­lus" (On-line). Am­phib­i­aWeb. Ac­cessed April 05, 2010 at http://​amphibiaweb.​org/​cgi/​amphib_​query?​where-genus=Hyperolius&​where-species=nitidulus.

Drewes, R. 1984. A phy­lo­ge­netic analy­sis of the Hy­per­oli­idae (Anura) : treefrogs of Africa, Mada­gas­car, and the Sey­chelles Is­lands. San Fran­cisco: Cal­i­for­nia Acad­emy of Sci­ences.

Geise, W., K. Lin­sen­mair. 1988. Adap­ta­tions of the Reed Frog Hy­per­olius virid­i­flavis (Am­phibia, Anura, Hy­per­oli­idae) to Its Arid En­vi­ron­ment. IV. Eco­log­i­cal sig­nif­i­cance of Water Econ­omy with Com­ments on Ther­moreg­u­la­tion and En­ergy Al­lo­ca­tion. Oe­colo­gia, 77, No. 3: 327-338. Ac­cessed April 05, 2010 at http://​www.​jstor.​org/​stable/​4218784.

Grafe, T., R. Schmuckt, K. Lisen­mair. 1992. Re­pro­duc­tive En­er­get­ics of the African Reed Frogs, Hy­per­olius virid­i­flavus and Hy­per­olius mar­mora­tus. Phys­i­o­log­i­cal Zo­ol­ogy, 65: 153-171. Ac­cessed Feb­ru­ary 20, 2010 at http://​www.​opus-bayern.​de/​uni-wuerzburg/​volltexte/​2009/​3118/​pdf/​Linsenmair_​Reproductive.​pdf.

Grafe, T., K. Lisen­mair. 1989. Pro­tog­y­nous Sex Change in the Reed Frog Hy­per­olius virid­i­flavus. Copeia, 4: 1024-1029. Ac­cessed Feb­ru­ary 20, 2010 at http://​www.​jstor.​org/​pss/​1445989.

Richards, C., B. Carl­son, S. Rogers. 1975. Re­gen­er­a­tion of dig­its and fore­limbs in the Kenyan reed frog Hy­per­olius virid­i­flavus fer­niquei Con­tri­bu­tion num­ber 52 from the Am­phib­ian Fa­cil­ity. Sup­ported in part by grants from the Mus­cu­lar Dy­s­tro­phy As­so­ci­a­tions of Amer­ica and NIH Grant No. 1 PO6 RR 00572 to George W. Nace.. Jour­nal of Mor­phol­ogy, 146: 431-445. Ac­cessed Feb­ru­ary 21, 2010 at <http://​hdl.​handle.​net/​2027.​42/​50260>.

Schiøtz, A. 1975. The Treefrogs of East­ern Africa. Copen­hagen: Steen­stru­pia.

Schiøtz, A. 1999. Treefrogs of Africa. Frank­furt am Main: Edi­tion Chi­maira.

Schiøtz, A. 2008. "Hy­per­olius virid­i­flavus" (On-line). Am­phib­i­aWeb. Ac­cessed Feb­ru­ary 20, 2010 at http://​amphibiaweb.​org/​cgi/​amphib_​query?​query_​src=aw_​lists_​soundInclude_&​where-genus=Hyperolius&​where-species=viridiflavus.

Schiøtz, A., A. Chan­ning, J. Poyn­ton, M. Largen. 2004. "Hy­per­olius virid­i­flavus" (On-line). IUCN Red List of Threat­ened Species. Ac­cessed Feb­ru­ary 20, 2010 at http://​www.​iucnredlist.​org/​apps/​redlist/​details/​56219/​0.

Schmuckt, R., K. Lisen­mair. 1988. Adap­ta­tions of the reed frog Hy­per­olius virid­i­flavus (Am­phibia, Anura, Hy­per­oli­idae) to its arid en­vi­ron­ment. Oe­colo­gia, 75: 354-361. Ac­cessed Feb­ru­ary 21, 2010 at http://​www.​jstor.​org/​pss/​4218582.

Wiec­zorek, A., R. Drewes, A. Chan­ning. 2001. Phy­lo­ge­netic re­la­tion­ships within the Hy­per­olius virid­i­flavus com­plex (Anura: Hy­per­oli­idae), and com­ments on tax­o­nomic sta­tus. Am­phibia-Rep­tilia, 22: 155-166. Ac­cessed Feb­ru­ary 19, 2010 at http://​www.​ingentaconnect.​com/​content/​brill/​amre/​2001/​00000022/​00000002/​art00002.