Pterocnemia pennatalesser rhea

Ge­o­graphic Range

Dar­win's Rhea only oc­curs in South Amer­ica--Patag­o­nia, in the Andes in Ar­gentina, Chile, Bo­livia and Peru. ( http://​www.​scz.​org/​pampas/​drhea1.​html)

Habi­tat

Dar­win's Rhea lives ex­clu­sively on the open plains of South Amer­ica, in areas of open scrub, like in the puna of the An­dean plateau, and also in the areas of steppe which ex­tend over the east­ern slope of the Andes and into the low­lands of Patag­o­nia. Dar­win's Rhea prefers to be near a lake, river or swamp for breed­ing, even though its habi­tats are quite arid. (del Hoyo, El­liot, and Sar­gatal, 1992)

Phys­i­cal De­scrip­tion

Dar­win's Rhea stands at 92.5 to 100 cm. It re­sem­bles the os­trich, al­though it is con­sid­er­ably smaller, and is there­fore some­times called the South Amer­i­can os­trich. Its wings are pro­por­tion­ally larger than those of other ratites, though it is also flight­less. It is able to manu­ver quite well when run­ning be­cause of its wings. It has three toes, and a strong claw on the end of each wing that is often used ef­fec­tively as a weapon. Its feath­ers are smooth and soft, and cover its thighs and the top of the tarsi. It has brown plumage with white fleck­ing through­out, though the fe­male is duller and has fewer white spots on the back. The ju­ve­nile is browner, with­out the white spot­ting. The typ­i­cal adult plumage is gained grad­u­ally in the third or fourth year. ( http://​www.​scz.​org/​pampas/​drhea1.​html; del Hoyo, El­liot, and Sar­gatal, 1992)

  • Range mass
    15 to 25 kg
    33.04 to 55.07 lb

Re­pro­duc­tion

The breed­ing sea­son for Dar­win's Rhea is fairly vari­able. At the onset of the sea­son, males com­pete for ter­ri­tory in short fights. After se­cur­ing ter­ri­tory, males at­tempt to at­tract fe­males into it by run­ning at them quickly with out­spread wings. When he has suc­ceeded in gath­er­ing 2-12 fe­males, he then be­gins a courtship dis­play, which in­volves var­i­ous calls and run­ning around them, shak­ing his wings. After cop­u­la­tion, the male leads the fe­males in a group to the nest, where they lay their eggs one after an­other. Then the fe­males leave, also in a group. In the weeks that fol­low, they re­turn every 2 or 3 days to de­posit more eggs. The eggs are yel­low­ish olive green, but fade to buff, and av­er­age 127x87 mm. Once lay­ing is over at a par­tic­u­lar nest, the fe­males leave to mate with an­other male and to lay eggs in the cor­re­spond­ing nest (del Hoyo, El­liot, and Sar­gatal, 1992). The male is then left on his own for in­cu­ba­tion and chick-rear­ing. In­cu­ba­tion be­gins 2-8 days after egg lay­ing be­gins, and may con­tinue for 35-40 days. The male be­comes ag­gres­sive to­ward any­thing that ap­proaches, in­clud­ing fe­males who come to lay more eggs, so often they just lay them nearby. The male rolls the near­est into the nest, but some re­main out of his reach and get left be­hind. Those rot­ting eggs at­tract flies, which be­come food for the male and the newly hatched chicks. The nest usu­ally ends up with 13-30 eggs. When one chick hatches, it be­gins call­ing, stim­u­lat­ing the oth­ers to hatch. Thus they all hatch syn­chro­nously in a pe­riod of 24-28 hours. The chicks are gray­ish brown with black­ish stripes, and the tarsi is fully feath­ered (del Hoyo, El­liot, and Sar­gatal, 1992).

The chicks are led away from the nest by the male after a few days, and they keep in touch by means of con­tact whis­tles. When­ever the chicks are in dan­ger, or too hot, or too cold at night, they ei­ther crouch on the ground or hide under the male's wings. The male is very pro­tec­tive. Lost chicks are often adopted by an­other male with his own chicks, which leads to a wide range of ages within one group. The pe­riod of parental care is 6 months, but the ju­ve­niles gen­er­ally re­main in their groups until they are sex­u­ally ma­ture at 2-3 years old (del Hoyo, El­liot, and Sar­gatal, 1992)

Be­hav­ior

Dar­win's Rhea is fairly so­cia­ble and lives in mixed groups of all ages and both sexes. They nor­mally travel in groups num­ber­ing 5-30 in­di­vid­u­als. Dur­ing the breed­ing sea­son, fe­males tend to break off into small groups while males be­come ter­ri­to­r­ial. It has been ob­served that a small per­cent­age of males go live alone in seclu­sion at an ad­vanced age (del Hoyo, El­liot, and Sar­gatal, 1992). Though they are so­cia­ble, in­di­vid­u­als must keep a cer­tain dis­tance away from each other, or else a "head-for­ward" threat dis­play may ensue. The head-for­ward threat dis­play in­volves the bird throw­ing its head for­ward and hiss­ing with its bill open. It oc­curs most often when the bird is sit­ting.

Dar­win's Rhea can reach speeds of 60 km/h. It is a strong swim­mer and has been ob­served to cross rivers. It has ex­cel­lent eye­sight and good hear­ing. Though it can eas­ily out­run preda­tors, it has a habit of re­trac­ing its steps when being pur­sued, and then sud­denly squat­ting down in the bushes and flat­ten­ing its body against the ground. De­spite its large size, it goes com­pletely un­no­ticed. An­other tac­tic it uses to con­fuse its preda­tors is to run in a zigza­g­ing pat­tern, or to turn sharply at right an­gles. Al­though it is fast, it has low sta­mina, and it runs with its neck hor­i­zon­tal and its wings folded in order to be able to pass more eas­ily through the bushes. It is di­ur­nal, with some ex­cep­tion dur­ing very hot pe­ri­ods (del Hoyo, El­liot, and Sar­gatal, 1992).

A rhea wan­ders while it feeds, and some­times groups with other wild her­bi­vores. This is ben­e­fi­cial for both par­ties be­cause the com­bi­na­tion of the rhea's good eye­sight with the lat­ter's good sense of smell helps them to de­tect preda­tors at a dis­tance more ef­fi­ciently.

Com­mu­ni­ca­tion and Per­cep­tion

Food Habits

The diet of Dar­win's Rhea con­sists of var­i­ous types of plant mat­ter, in­clud­ing roots, fruits, seeds, and leaves. A small per­cent­age of an­i­mal mat­ter is also con­sumed, in­clud­ing in­sects and small ver­te­brates. It drinks lit­tle water, be­cause most of the liq­uid re­quire­ments are sat­is­fied by plants. It also in­gests peb­bles. It does not have to move around a lot for food, be­cause the abun­dance of veg­e­ta­tion in its habi­tat means that it gen­er­ally has suf­fi­cient re­sources all year long (del Hoyo, El­liot, and Sar­gatal, 1992).

Eco­nomic Im­por­tance for Hu­mans: Pos­i­tive

The rhea's habit of wan­der­ing around with cat­tle can be ben­e­fi­cial to farm­ers be­cause it often eats burr-like seeds that be­come en­tan­gled in sheep's wool. It is some­times used for food, and some parts are used for med­i­cine. It is also used for com­mer­cial ends, es­pe­cially the feath­ers. The skin is used for rugs and more com­monly for burn­ing--the smoke pro­duced is be­lieved to be ben­e­fi­cial to the coca plants.

Con­ser­va­tion Sta­tus

It is hunted for its feath­ers, meat, eggs and other body parts. Its habi­tat is being de­stroyed by agri­cul­ture. In some min­ing areas, they are hunted from jeeps. (del Hoyo, El­liot, and Sar­gatal, 1992; http://​www.​scz.​org/​pampas/​drhea1.​html)

Other Com­ments

Dar­win's Rhea lives about 20 years in the wild, and 40 in cap­tiv­ity. Its toes are good luck charms in South Amer­ica.

Con­trib­u­tors

Ali­cia Ivory (au­thor), Uni­ver­sity of Michi­gan-Ann Arbor.

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.

chemical

uses smells or other chemicals to communicate

endothermic

animals that use metabolically generated heat to regulate body temperature independently of ambient temperature. Endothermy is a synapomorphy of the Mammalia, although it may have arisen in a (now extinct) synapsid ancestor; the fossil record does not distinguish these possibilities. Convergent in birds.

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).

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.

scrub forest

scrub forests develop in areas that experience dry seasons.

sexual

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

tactile

uses touch to communicate

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

del Hoyo, J., El­liot, A., and Sar­gatal, J. Hand­book of the Birds of the World, Vol. 1. Lynx Edi­cions, Barcelona, 1992.

http://​www.​scz.​org/​pampas/​drhea1.​html