Coereba flaveolabananaquit

Ge­o­graphic Range

Co­ereba flave­ola (ba­nanaquit) is com­mon mainly in South Amer­ica. It is most often found within the range from south­ern Mex­ico to north­ern Ar­gentina and largely east­ward through­out South Amer­ica. It oc­cu­pies most of the Caribbean Is­lands and on rare oc­ca­sions is found in Florida (Merola-Zwart­jes 1998).

Habi­tat

The ba­nanaquit cov­ers a range of habi­tats within its ge­o­graph­i­cal area. The birds are most com­monly found at low el­e­va­tions and rarely in the high moun­tain­ous forests. They are pre­sent in open fields, areas of cover, the dense, humid rain forests, and even in cer­tain desert areas. Ob­servers have spot­ted the ba­nanaquit at a va­ri­ety of el­e­va­tions, rang­ing from sea level up to 4000 ft, but is most com­monly seen in the low­lands (usu­ally below 760 ft). Al­though, C. flave­ola is pre­sent in many habi­tats, it is most com­mon in the trop­i­cal re­gion in areas with some cover (Allen 1961; Wun­derle 1984).

Phys­i­cal De­scrip­tion

The tiny adult ba­nanaquit ranges from about 10.5 to 11.5 cm in length. It has a dark, slen­der, curved beak. Al­though its plumage varies slightly across its ge­o­graphic range, the adult plumage is nearly sex­u­ally monomor­phic. In the male, the feath­ers on the above side are dark gray, while its crown is more black and the un­der­side/rump is bright yel­low. A long, promi­nent, white eye­brow (su­per­cil­ium) sits di­rectly above the eye and many times a white spot (specu­lum) oc­curs on its gen­er­ally black wings. The throat is a lighter shade of gray than the back and in cer­tain races the tail-feath­ers are tipped white. The fe­male ba­nanaquit is very sim­i­lar, ex­cept that her crown is nar­rowly darker, her throat whitish as op­posed to gray, and her rump is more of an olive-yel­low shade. The young ba­nanaquit has feath­ers that are far more dull than its par­ents' and ap­pear more olive-yel­low over its en­tire body. Cer­tain races of the ba­nanaquit tend to be en­tirely black, while oth­ers lack cer­tain col­ors or de­f­i­n­i­tion in their plumage (Allen 1961; Ridgely and Tudor 1989; Fjeldsa and Krabbe 1990).

Re­pro­duc­tion

Re­pro­duc­tion varies slightly among the sub­species of C. flave­ola. Typ­i­cally, though, the ba­nanaquit will raise sev­eral broods within a year and gen­er­ally the breed­ing sea­son lasts for five months. In cer­tain areas the ba­nanaquit breeds at the end of the dry sea­son (March through early Au­gust). Breed­ing is also often syn­chro­nized with the first rains early in the wet sea­son. Other times, though, breed­ing does not show any re­la­tion­ship to the sea­sonal weather pat­terns.

Ba­nanaquit broods may con­tain from one to three eggs. The eggs them­selves are a white-cream color (some­times pink­ish) with brown/salmon spots that vary in dis­tri­b­u­tion (Allen 1961; Wun­derle 1984).

Lifes­pan/Longevity

Be­hav­ior

The ba­nanaquit, a fast-paced, seem­ingly ner­vous bird, is not colo­nial. It tends to be soli­tary and no­madic. It does not show any ev­i­dence of claim­ing in­di­vid­ual ter­ri­to­ries. Males court fe­males, for the most part, with­out act­ing at all de­fen­sively to­wards other males, which char­ac­ter­izes poly­ter­ri­torism.

The bird, in areas where it is most com­mon, may be­come very tame around human set­tle­ments. Na­tives of South Amer­ica find, from time to time, the ba­nanaquit on their kitchen table look­ing for sugar. Its song is char­ac­ter­ized as "in­sect-like," twit­ter­ing, and shrill.

Both the male and fe­male ba­nanaquit build their own globe-shaped nests using leaves, grasses, and plant fibers. The dis­tinc­tive nests have a side en­trance hole and are lined with bits of smaller mat­ter (thread, paper, feath­ers, spi­der web­bing, etc.).

Nest­ing gen­er­ally goes on through­out the year, each sex de­fend­ing a small area sur­round­ing its own roost­ing nest. Prior to breed­ing the male spends his time singing around his own nest and also in the area sur­round­ing a fe­male's nest to at­tract her as a mate. There is ev­i­dence that the breed­ing pairs par­take in some form of courtship rit­ual, which often in­cludes fac­ing each other, bow­ing, turn­ing heads, scrap­ing, and fly­ing in a num­ber of di­rec­tions.

Be­fore a fe­male lays her eggs, the male re­mains very close (within 2 m) to his mate. He is very pro­tec­tive as they feed and gather ma­te­ri­als for a brood­ing nest (dif­fer­ent from her roost­ing nest). Once the eggs have been laid and in­cu­ba­tion has begun the male be­comes far less at­ten­tive. He goes back to singing in the vicin­ity of his own nest and court­ing other fe­males.

At one time the ba­nanaquit was thought to be monog­a­mous, how­ever now mate switch­ing is rec­og­nized as a com­mon prac­tice.

Al­though the males never as­sist in in­cu­bat­ing and most of the feed­ing and other care is done by the fe­male, some males will help in feed­ing and pro­tec­tion. Fe­males, though, play the major role in pro­tect­ing the broods from other male and fe­male ba­nanaquits, as well as other nest preda­tors (in­clud­ing ants, rats, and snakes). (Allen, 1961; Ridgely and Tudor, 1989; Wun­derle, 1984)

Com­mu­ni­ca­tion and Per­cep­tion

Food Habits

Co­ereba flave­ola, often com­pared to hum­ming­birds, takes flower nec­tar as its pri­mary source of food. Al­though it does use its sharp beak to pierce flow­ers from the side to feed, much like some hum­ming­birds, the ba­nanaquit can­not hover like a hum­ming­bird. For this rea­son the bird must al­ways perch while feed­ing and many times hangs up­side down from a branch in­stead of sit­ting up­right. In ad­di­tion to nec­tar, it eats a num­ber of other food items that in­clude fruits, in­sects, and other small arthro­pods. The ba­nanaquit en­joys many kinds of fruit, in­clud­ing ripe ba­nanas. It may also pick small in­sects from the un­der­sides of leaves and eats flies, bee­tles, cater­pil­lars, ants, bees, and spi­ders (Allen 1961; Skutch and Stiles 1989).

Eco­nomic Im­por­tance for Hu­mans: Pos­i­tive

Co­ereba flave­ola does not ben­e­fit hu­mans in many ways. Re­cent stud­ies have shown that ba­nanaquits, in ad­di­tion to hum­ming­birds, pol­li­nate at least three species of Brome­lioideae (a sub­fam­ily of bromeliad plants).

Peurto Rico has adopted the ba­nanaquit as its na­tional bird, and many Caribbean and South Amer­i­can coun­tries have fea­tured the bird on their postage stamps (Saz­ima and Saz­ima 1999).

Eco­nomic Im­por­tance for Hu­mans: Neg­a­tive

Ba­nanaquits often get to flower nec­tar through the side of the flower. It pierces the flower and re­trieves the nec­tar for its own ben­e­fit. This means that the flower is ei­ther left un­pol­li­nated or will die (Skutch and Stiles 1989).

Con­ser­va­tion Sta­tus

Co­ereba flave­ola does not ap­pear to be en­dan­gered in any way across its ge­o­graphic range. It is a rather abun­dant species in the areas in which it oc­curs.

Other Com­ments

As ba­nanaquits cover a wide ge­o­graphic range made up largely of is­lands, there are a num­ber of sub­species. In the Caribbean re­gion the species has a "highly vari­able phe­no­type." This long chain of is­lands could only have been pop­u­lated through a process of over-wa­ter dis­per­sal. Each is­land has ended up with its own sub­species of ba­nanaquit. Two main groups are rec­og­nized. The Ba­hamian group in­cludes the Ba­hamas (C.f. ba­hamen­sis), Cay­man Is­lands (C. f. sharpei), coastal is­lands off of Yu­catan (C. f. caboti), and a few oth­ers. The An­til­lean group in­cludes Puerto Rico (C. f. por­tori­cen­sis), St. Croix (C. f. new­toni), Bar­ba­dos (C. f. bar­baden­sis), and a few oth­ers. The sub­species vary mostly in plumage.

In­ter­est­ingly, the highly suc­cess­ful ba­nanaquit in­hab­its ba­si­cally every is­land in the Caribbean ex­cept for Cuba.

Bi­ol­o­gists place C. flave­ola in its own group be­tween the war­bler and tan­ager groups (Allen 1961; Morse 1989; Seutin and Gilles 1994).

Con­trib­u­tors

Erin Hay­den (au­thor), Uni­ver­sity of Michi­gan-Ann Arbor, Phil Myers (ed­i­tor), Mu­seum of Zo­ol­ogy, 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.

forest

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

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.

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.

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

Allen, R. 1961. Birds of the Caribbean. New York: The Viking Press.

Fjeldsa, J., N. Krabba. 1990. Birds of the High Andes. Svend­borg, Den­mark: Zo­o­log­i­cal Mu­seum, Uni­ver­sity of Copen­hagen, and Apollo Books.

Merola-Zwart­jes, M. July 1998. Meta­bolic rates, tem­per­a­ture reg­u­la­tion, and the en­er­getic im­pli­ca­tions of roost nests in the Ba­hamas (*Co­ereba flave­ola*). Auk, 115(3): 432-433.

Morse, D. 1989. Amer­i­can War­blers. Cam­bridge, Mass­a­chu­setts: Har­vard Uni­ver­sity Press.

Ridgely, R., G. Tudor. 1989. The birds of South Amer­ica: the os­cine passer­ines (Vol 1). Austin, Texas: Uni­ver­sity of Texas Press.

Saz­ima, M., I. Saz­ima. Jan­u­ary 1999. The perch­ing bird of *Co­ereba flave­ola* as a co-pol­li­na­tor of bromeliad flow­ers in south­east­ern Brazil. Cana­dian Jour­nal of Zo­ol­ogy, 77(1): 45-51.

Seutin, , Gilles. Au­gust 1994. His­tor­i­cal Bio­geog­ra­phy of the Ba­nanaquit in the Caribbean Re­gion: A Mi­to­chon­dr­ial DNA As­sess­ment. Evo­lu­tion, 48(4): 1043.

Stiles, F., A. Skutch. 1989. A Guide to the Birds of Costa Rica. Ith­ica, New York: Cor­nell Uni­ver­sity Press.

Wun­derle, J. 1984. Mate switch­ing and a sea­sonal in­crease in polyg­yny in the ba­nanaquit. Be­hav­iour, 88(1-2): 123-144.