Setophaga ruticillaAmerican redstart

Ge­o­graphic Range

Com­monly known as Amer­i­can red­starts, Se­tophaga ru­ti­cilla is a Neotrop­i­cal mi­grant war­bler that spends por­tions of the year in both the Nearc­tic and the Neotrop­i­cal re­gions. Dur­ing the spring and sum­mer, Se­tophaga ru­ti­cilla breeds across much of Canada and the United States. It in­hab­its the south­ern re­gions of Canada from the east to west coast. In the United States, Se­tophaga ru­ti­cilla may be found in lim­ited re­gions of the north­ern Mid­west, and most states east of the Mis­sis­sippi River. Ex­clu­sions in­clude por­tions of Ken­tucky, Ten­nessee, Florida, Geor­gia, and North and South Car­olina. This species mi­grates bian­nu­ally across much of the United States and Cen­tral Amer­ica to reach its win­ter­ing grounds in south­ern Cen­tral and north­west­ern South Amer­ica. Se­tophaga ru­ti­cilla also over­win­ters on many Caribbean is­lands in­clud­ing Ja­maica and Cuba. (Sherry and Holmes, 1997)

Habi­tat

Se­tophaga ru­ti­cilla se­lects vary­ing habi­tats de­pend­ing on the sea­son and ge­o­graphic lo­ca­tion. Dur­ing the breed­ing sea­son, this war­bler in­hab­its open-canopy, mostly de­cid­u­ous forests, sec­ond growth, and for­est edge across much of the United States and south­ern Canada. This in­sec­tiv­o­rous bird often shares its for­ag­ing habi­tats with other war­blers, and is found feed­ing in the mid to lower re­gions of a tree or shrub. Se­tophaga ru­ti­cilla prefers to build its nest well within dense shrubs or the fork of a low tree, and males will se­lect ter­ri­to­ries that con­tain sev­eral of these po­ten­tial nest sites.

Dur­ing mi­gra­tion, Se­tophaga ru­ti­cilla stopover in dense shrubby habi­tats where food is abun­dant. On their win­ter­ing grounds in Cen­tral and South Amer­ica, this war­bler may be found in nearly all woody habi­tats but tend to avoid non-forested agri­cul­tural areas. It is often found in shade-grown cof­fee plan­ta­tions which pro­vide na­tive trees and shrubs, as well as cof­fee trees. El­e­va­tions oc­cu­pied vary by lo­ca­tion, as this species may be found at el­e­va­tions up to 3,000 m in South Amer­ica, but only up to 1,500 in Ja­maica. Dur­ing the non-breed­ing sea­son, Se­tophaga ru­ti­cilla is in­flu­enced by strong dom­i­nance hi­er­ar­chies that re­sult in sex­ual habi­tat seg­re­ga­tion. Older males ex­hibit the most dom­i­nant be­hav­ior and will oc­cupy pre­ferred, re­source-abun­dant habi­tats (man­groves). Fe­males and other sub­or­di­nate in­di­vid­u­als are thus re­stricted to lower qual­ity habi­tats (scrub), which re­sults in greater mass loss and lower sur­vivor­ship rates dur­ing the non-breed­ing sea­son. Stud­ies have shown that in pre­ferred habi­tats, sex ratio is 3:2 (mostly males) while in lower qual­ity the ratio is 1:3 (mostly fe­males). (Ehrlich, et al., 1988; Marra and Holmes, 2001; Sherry and Holmes, 1997)

  • Range elevation
    3,000 (high) m
    ft

Phys­i­cal De­scrip­tion

Se­tophaga ru­ti­cilla is a smaller war­bler mea­sur­ing 13.3 cm in length and weigh­ing 8.3 g. Adult males have mostly black up­per­parts with bold patches of or­ange. The sides of breast, bases of wing feath­ers, and bases of the outer tail feath­ers fea­ture large patches of bright or­ange. The belly and un­der­tail coverts are white. Adult fe­males fea­ture the same pat­tern, but have mostly gray up­per­parts with patches of bright yel­low or or­ange in older fe­males. They have olive-col­ored backs and the wings and tail feath­ers are a darker gray than the head. Throat, belly, and un­der­tail coverts are pale gray to white. First year males closely re­sem­ble fe­males and will ob­tain adult male plumage after the first breed­ing sea­son. Fe­males and young males may also fea­ture a slight white eye-ring and pale su­per­cil­lium. All sexes and ages have black legs, feet and bills. The short bill is very sim­i­lar to in­sect-eat­ing fly­catch­ers in being rel­a­tively flat and sur­rounded by ric­tal bris­tles. ("Na­tional Ge­o­graphic Com­plete Birds of North Amer­ica", 2006; Sherry and Holmes, 1997; Sib­ley, 2000)

  • Sexual Dimorphism
  • sexes colored or patterned differently
  • male more colorful
  • Range mass
    6 to 9 g
    0.21 to 0.32 oz
  • Average mass
    8.3 g
    0.29 oz
  • Range length
    11 to 14 cm
    4.33 to 5.51 in
  • Average length
    13.3 cm
    5.24 in
  • Average wingspan
    19.7 cm
    7.76 in

Re­pro­duc­tion

Like most war­blers, Se­tophaga ru­ti­cilla is pre­dom­i­nantly monog­a­mous with rare cases of polygamy. Three stages of courtship have been de­scribed: pair-for­ma­tion, pre-nest build­ing, and nest build­ing. Pair-for­ma­tion typ­i­cally be­gins im­me­di­ately after fe­males ar­rive on the breed­ing grounds. Males aeri­ally chase po­ten­tial mates, who will only fly a short dis­tance and then per­form a tail-spread­ing dis­play and give harsh chip notes. Once es­tab­lished, pairs will visit po­ten­tial nest sites within the male's ter­ri­tory. Nest sites are se­lected by fe­males, and males will closely fol­low fe­males dur­ing this pe­riod, pre­sum­ably to guard them from other males. Males give two main types of dis­plays dur­ing nest-build­ing: fluff dis­plays and bow dis­plays. Fluff dis­plays in­volve rais­ing the feath­ers on the head and back, while feath­ers are sleek for bow dis­plays and the male will lower his body to the ground while keep­ing his head ver­ti­cal and tail spread. (Ehrlich, et al., 1988; Ficken, 1963; Sherry and Holmes, 1997)

Se­tophaga ru­ti­cilla is a Neotrop­i­cal mi­grant that trav­els to North Amer­ica to breed in the spring. Courtship and pair-for­ma­tion be­gins within a week of the ar­rival of fe­males, which oc­curs from mid- to late May. After a pair has formed, the fe­male alone se­lects the nest site which is typ­i­cally up against a tree trunk, hid­den in dense veg­e­ta­tion. The cup-shaped nest con­sists of tightly-wo­ven, fine ma­te­ri­als such as grass, feath­ers, roots, birch bark, or an­i­mal hair. Once the nest is com­plete, the fe­male lays be­tween 2 and 5 white or cream-col­ored eggs which are speck­led with vary­ing amounts of brown. The clutch is in­cu­bated by the fe­male for 10 to 13 days. The young fledge after 9 days in the nest, and may re­main with one par­ent for up to 3 weeks after fledg­ing. First-year males are able to re­pro­duce dur­ing their first breed­ing sea­son, but they re­tain the fe­male-like plumage which may con­tribute to low re­pro­duc­tive suc­cess (less than 50% of first-year males) until year 2. In con­trast, most first-year fe­males suc­cess­fully re­pro­duce dur­ing their first breed­ing sea­son. There is ev­i­dence for a skewed sex ratio that re­sults in a sur­plus of un­mated males. (Ehrlich, et al., 1988; Sherry and Holmes, 1997)

  • Breeding interval
    American redstarts breed once yearly
  • Breeding season
    The breeding season for American redstarts occurs from mid- or late May through the end of July
  • Range eggs per season
    2 to 5
  • Average eggs per season
    4
  • Range time to hatching
    10 to 13 days
  • Average time to hatching
    12 days
  • Average fledging age
    9 days
  • Range time to independence
    3 (high) weeks
  • Average age at sexual or reproductive maturity (female)
    <1 years
  • Average age at sexual or reproductive maturity (male)
    <1 years

Male Se­tophaga ru­ti­cilla are very ter­ri­to­r­ial and will ac­tively de­fend their ter­ri­to­ries, mates, and young. Fe­males se­lect a suit­able nest­ing site and con­struct the en­tire nest alone. Once eggs are laid, fe­males also per­form all in­cu­ba­tion for an av­er­age of 12 days. The young are al­tri­cial at birth and thus re­quire sig­nif­i­cant parental in­vest­ment. The help­less hatch­lings are brooded by the fe­male alone, as the male lacks a brood patch. Both par­ents par­tic­i­pate equally in feed­ing the young, and each mate makes be­tween 4 and 13 feed­ing trips per hour. Both par­ents also re­move fecal sacs from the nest to re­duce pre­da­tion and keep san­i­tary nest con­di­tions. After the young fledge at 9 days of age, each par­ent typ­i­cally cares for cer­tain off­spring only. The two par­ents often sep­a­rate with their re­spec­tive young, al­though the male typ­i­cally stays near the nest site. (Ehrlich, et al., 1988; Sherry and Holmes, 1997)

One study has demon­strated a cor­re­la­tion be­tween male col­oration and level of parental in­vest­ment. Male Se­tophaga ru­ti­cilla that fea­tured brighter or­ange col­oration on the flanks made sig­nif­i­cantly more trips to the nest and over­all spent more time at the nest. There­fore, male flank col­oration may play a role in sex­ual se­lec­tion and may ex­plain why first-year males have low lev­els of re­pro­duc­tive suc­cess until they ob­tain their adult, black and or­ange col­oration. (Ger­main, et al., 2010)

  • Parental Investment
  • altricial
  • male parental care
  • female parental care
  • pre-fertilization
    • provisioning
    • protecting
      • male
      • female
  • pre-hatching/birth
    • provisioning
      • male
      • female
    • protecting
      • male
      • female
  • pre-weaning/fledging
    • provisioning
      • male
      • female
    • protecting
      • male
      • female
  • pre-independence
    • provisioning
      • male
      • female
    • protecting
      • male
      • female

Lifes­pan/Longevity

The old­est Se­tophaga ru­ti­cilla on record was a male banded in adult plumage (mak­ing it at least 2 years old) which was re-cap­tured ap­prox­i­mately 9 years later, mak­ing it at least 10 years old. There is ev­i­dence that many fe­males live to be at least 5. Se­tophaga ru­ti­cilla is not kept in cap­tiv­ity and thus there is no data for cap­tive lifes­pan. An­nual sur­vival rates are es­ti­mated to be be­tween 50 and 60%. Fe­males are thought to suf­fer a slightly higher mor­tal­ity rate as they spend sig­nif­i­cantly more time on the nest (brood­ing) and are often con­sumed by nest preda­tors. (Sherry and Holmes, 1997)

  • Range lifespan
    Status: wild
    10 (high) years
  • Typical lifespan
    Status: wild
    5 to 10 days

Be­hav­ior

Se­tophaga ru­ti­cilla is a Neotrop­i­cal war­bler that makes a bian­nual jour­ney be­tween Cen­tral or South Amer­ica and the United States or Canada. It is an ac­tive species that is often glimpsed while it flits about within dense veg­e­ta­tion. Se­tophaga ru­ti­cilla is known for it's dis­tinc­tive for­ag­ing be­hav­ior of flick­ing it's brightly col­ored tail to stir up in­sects from fo­liage. Like most Neotrop­i­cal mi­grants, this war­bler per­forms long mi­gra­tions at night but is di­ur­nal out­side of the mi­gra­tory pe­riod. It is a highly ter­ri­to­r­ial species, and will vig­or­ously de­fend ter­ri­tory dur­ing the breed­ing and non-breed­ing sea­sons. Dur­ing the non-breed­ing sea­son, higher-ranked males will oc­cupy higher qual­ity habi­tats such as moist man­groves. Fe­males and sub­or­di­nate males are chased out to habi­tats of lower qual­ity in­clud­ing dry scrub forests. Males that are higher in the hi­er­ar­chy typ­i­cally are older, have more ex­ten­sive black bibs, and brighter or­ange col­oration. Likely due to it's highly ter­ri­to­r­ial na­ture, this species is rarely seen with more than one other Se­tophaga ru­ti­cilla. How­ever, dur­ing mi­gra­tion it will often join multi-species groups. (Marra and Holmes, 2001; Sherry and Holmes, 1997)

  • Range territory size
    0.01 (high) km^2

Home Range

Se­tophaga ru­ti­cilla typ­i­cally de­fends a breed­ing ter­ri­tory of less than 1 hectare. Size may vary with habi­tat qual­ity, pop­u­la­tion den­sity, and age of de­fend­ing male. (Sherry and Holmes, 1997)

Com­mu­ni­ca­tion and Per­cep­tion

Se­tophaga ru­ti­cilla pri­mar­ily uses vocal and vi­sual forms of com­mu­ni­ca­tion. Male Se­tophaga ru­ti­cilla give dis­tinc­tive songs which are used to de­fend ter­ri­tory or at­tract mates. Songs of this species are highly vari­able but are gen­er­ally rapid and high pitched. Songs may re­peat the same 1 or 2 phrases or have 2 to 8 dif­fer­ent phrases given in rapid suc­ces­sion. Some songs end in an ac­cented, ter­mi­nal note while oth­ers sim­ply end un­ac­cented. Se­tophaga ru­ti­cilla uses these dif­fer­ent song types to com­mu­ni­cate in dif­fer­ent sit­u­a­tions. Re­peated songs with ac­cented end­ings are typ­i­cally used for at­tract­ing mates, or while males are in close prox­im­ity to their mates. Un­mated males usu­ally use only this song type. After males se­cure a mate, they then switch to singing se­r­ial songs to de­fend their ter­ri­to­ries against neigh­bor­ing birds. Like many birds, a sig­nif­i­cant amount of song vari­a­tion is due to local di­alects. Many Se­tophaga ru­ti­cilla in­di­vid­u­als can be iden­ti­fied by dis­tinct char­ac­ter­is­tics of their song such as pat­tern, fre­quency, or dis­tinc­tive syl­la­bles. Males of this species can quickly learn the songs of neigh­bor­ing ri­vals and in­cor­po­rate them into their own songs, lead­ing to unique neigh­bor­hood di­alects.

Se­tophaga ru­ti­cilla also uses body pos­tures and move­ments as com­mu­ni­ca­tion. Dur­ing courtship, males will often chase po­ten­tial mates in a some­what ag­gres­sive man­ner and in­ter­ested fe­males will re­spond by fly­ing a short dis­tance, then giv­ing a tail-spread­ing dis­play. Males often give two types of dis­plays to­wards fe­males: fluff dis­plays and bows. Fluff dis­plays con­sist of fluff­ing the body feath­ers, par­tic­u­larly the bright or­ange flanks. There is ev­i­dence that brighter or­ange flanks cor­re­late to higher lev­els of male parental in­vest­ment, and rais­ing these feath­ers may serve to ad­ver­tise parental qual­ity. Bow dis­plays are typ­i­cally given later in courtship, when a male sleeks his feath­ers, low­ers his breast to the ground, and holds his head ver­ti­cally.

This species is highly ter­ri­to­r­ial year-round and em­ploys song, body pos­tures, and aer­ial at­tacks to deter in­trud­ers. As dis­cussed above, males often ad­ver­tise ter­ri­tory bound­aries through singing, but fe­males also give a va­ri­ety of chips and short notes to­wards in­trud­ers. Both males and fe­males as­sume threat­en­ing body pos­tures in­clud­ing head-for­ward dis­plays with droop­ing wings and bill agape, and tail-spread­ing dis­plays with tail held near ver­ti­cally. Males also give a wings-out dis­play where they raise and spread their wings, likely to dis­play the or­ange wing patches. Males also make dis­tinc­tive cir­cling flights dur­ing ter­ri­to­r­ial dis­putes. Two neigh­bor­ing males (oc­ca­sion­ally fe­males) will al­ter­nate short, de­lib­er­ate, cir­cling flights in pur­suit of each other.

Like most birds, Se­tophaga ru­ti­cilla per­ceives the en­vi­ron­ment through au­di­tory, vi­sual, tac­tile, and chem­i­cal stim­uli. (Ficken, 1962; Sherry and Holmes, 1997)

Food Habits

Se­tophaga ru­ti­cilla is nearly ex­clu­sively in­sec­tiv­o­rous, but will oc­ca­sion­ally con­sume berries or seeds dur­ing the fall when in­sect abun­dance de­creases. Mor­pho­log­i­cally, the flat­tened beak and ric­tal bris­tles are sim­i­lar to old and new world fly­catch­ers (Mus­c­i­cap­i­dae and Tyran­nidae, re­spec­tively) and thus these species share sim­i­lar for­ag­ing be­hav­iors and diets. Se­tophaga ru­ti­cilla em­ploys the fo­liage glean­ing method to cap­ture prey and often flicks its brightly-pat­terned tail to flush sta­tion­ary prey. Fly­ing prey is then pur­sued and caught aeri­ally, after which the bird lands on a dif­fer­ent perch than it alighted from. Se­tophaga ru­ti­cilla is known for highly en­er­getic for­ag­ing habits and is often seen rapidly hop­ping through all heights of veg­e­ta­tion. It prefers to for­age from twigs and branches ver­sus tree trunks or limbs. Over­all, this species is a very flex­i­ble, op­por­tunis­tic feeder that can eas­ily adapt to vary­ing habi­tat, sea­son, in­sect com­mu­nity, veg­e­ta­tion struc­ture, and time of day. Diet con­sists largely of cater­pil­lars, moths, flies, leafhop­pers and plan­thop­pers, small wasps, bee­tles, aphids, stone­flies, and spi­ders. Few berries and seeds are con­sumed, but are most often from bar­berry (Berberis), ser­vice­berry (Ame­lanchier), and mag­no­lia (Mag­no­lia). (Ehrlich, et al., 1988; Sherry and Holmes, 1997)

  • Animal Foods
  • insects
  • terrestrial non-insect arthropods
  • Plant Foods
  • seeds, grains, and nuts
  • fruit

Pre­da­tion

Se­tophaga ru­ti­cilla is vul­ner­a­ble to both ter­res­trial and aer­ial preda­tors. High­est rates of pre­da­tion occur dur­ing the breed­ing sea­son when eggs and help­less nestlings are abun­dant and easy prey for ter­res­trial preda­tors. Fe­males mostly brood dur­ing this pe­riod and thus often fall prey to nest preda­tors. Com­mon ter­res­trial preda­tors in­clude red squir­rels, fish­ers, east­ern chip­munks, black bears, fly­ing squir­rels, fox snakes, and do­mes­tic cats. Aer­ial preda­tors take nestlings, eggs, or even adults in flight. Pos­si­ble aer­ial preda­tors in­clude jaegers, blue jays, com­mon ravens, north­ern saw-whet owls, com­mon grack­les, north­ern goshawks, and sharp-shinned hawks, and Cooper's hawks. (Mc­Cal­lum and Han­non, 2001; Sherry and Holmes, 1997)

Ecosys­tem Roles

As an in­sec­ti­vore, Se­tophaga ru­ti­cilla con­sumes sig­nif­i­cant amounts of in­sects and likely has an im­pact on local in­sect com­mu­ni­ties. This species also con­sumes small amounts of fruits and seeds dur­ing the fall which may con­tribute to seed dis­tri­b­u­tion for the plant species it feeds upon. Eggs, nestlings, and adults are con­sumed by a wide va­ri­ety of preda­tors. Like many birds, this species is host to sev­eral ec­topar­a­sites in­clud­ing three lice species and one tick. Se­tophaga ru­ti­cilla is a com­mon host for brown-headed cow­birds and cur­rently will ac­cept and suc­cess­fully raise cow­bird chicks. Pop­u­la­tions of Se­tophaga ru­ti­cilla that are ex­posed to Molothrus ater will react more ag­gres­sively to adults than pop­u­la­tions that have en­coun­tered them less often. (Ehrlich, et al., 1988; Sherry and Holmes, 1997)

Com­men­sal/Par­a­sitic Species

Eco­nomic Im­por­tance for Hu­mans: Pos­i­tive

Se­tophaga ru­ti­cilla is a com­mon vis­i­tor to shade-grown cof­fee plan­ta­tions in Cen­tral and South Amer­ica. These in­sec­tiv­o­rous war­blers are at­tracted to the ample veg­e­ta­tion pro­vided on these plan­ta­tions and will con­sume large amounts of crop pests. This species, along with other in­sec­ti­vores, help to re­duce farmer re­liance on pes­ti­cides. (Sherry and Holmes, 1997)

  • Positive Impacts
  • controls pest population

Eco­nomic Im­por­tance for Hu­mans: Neg­a­tive

There are no known ad­verse ef­fects of Se­tophaga ru­ti­cilla on hu­mans.

Con­ser­va­tion Sta­tus

Se­tophaga ru­ti­cilla is listed as least con­cern by the In­ter­na­tional Union for Con­ser­va­tion of Na­ture and Nat­ural Re­sources (IUCN) an ac­count of its wide ge­o­graphic range and rel­a­tively sta­ble pop­u­la­tion size. Re­cent pop­u­la­tion data how­ever, has shown this species to be in slight de­cline and num­bers should be mon­i­tored closely in the fu­ture. Like many de­clin­ing Neotrop­i­cal mi­grants, this species likely suf­fers from habi­tat loss on both the win­ter­ing and breed­ing grounds. The main causes for habi­tat loss is log­ging for human con­ver­sion of land to urban or res­i­den­tial areas. Se­tophaga ru­ti­cilla also prefers shrubby, early-suc­ces­sional habi­tats which nat­u­rally age and progress to ma­ture forests which are less suit­able. This species also suf­fers sig­nif­i­cant fa­tal­i­ties from im­pacts with man-made struc­tures dur­ing night mi­gra­tion. Over four fall mi­gra­tions, two tow­ers in Florida ac­counted for over 1,600 Se­tophaga ru­ti­cilla deaths. Se­tophaga ru­ti­cilla is also a com­mon host for brown-headed cow­birds which de­crease re­pro­duc­tive suc­cess. Cur­rently, there are few con­ser­va­tion ef­forts being made for this species, as it is still of least con­cern. In gen­eral, ef­forts are being made to cre­ate sus­tain­able log­ging prac­tices that sup­port the cre­ation of early-suc­ces­sional habi­tat. Sus­tain­able farm­ing prac­tices, such as shade-grown cof­fee, are be­com­ing more preva­lent on Cen­tral and South Amer­i­can coun­tries that strike a bal­ance be­tween agri­cul­ture and pro­vid­ing habi­tat for song­birds. Many local Audubon chap­ters are pro­mot­ing "lights out" cam­paigns that work with busi­nesses to turn lights off in large sky­scrap­ers dur­ing peak mi­gra­tion sea­son, which re­duces mi­grat­ing bird col­li­sions and fa­tal­i­ties. (Sherry and Holmes, 1997)

Con­trib­u­tors

Rachelle Ster­ling (au­thor), Spe­cial Pro­jects, Tanya Dewey (ed­i­tor), Uni­ver­sity of Michi­gan-Ann Arbor, George Ham­mond (ed­i­tor), An­i­mal Di­ver­sity Web Staff, Tri­cia Jones (ed­i­tor), Uni­ver­sity of Michi­gan-Ann Arbor, ADW Zookeeper (ed­i­tor), Uni­ver­sity of Michi­gan-Ann Arbor.

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

Neotropical

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

World Map

acoustic

uses sound to communicate

agricultural

living in landscapes dominated by human agriculture.

altricial

young are born in a relatively underdeveloped state; they are unable to feed or care for themselves or locomote independently for a period of time after birth/hatching. In birds, naked and helpless after hatching.

arboreal

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

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

chemical

uses smells or other chemicals to communicate

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

ranking system or pecking order among members of a long-term social group, where dominance status affects access to resources or mates

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.

female parental care

parental care is carried out by females

forest

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

insectivore

An animal that eats mainly insects or spiders.

introduced

referring to animal species that have been transported to and established populations in regions outside of their natural range, usually through human action.

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).

male parental care

parental care is carried out by males

migratory

makes seasonal movements between breeding and wintering grounds

monogamous

Having one mate at a time.

motile

having the capacity to move from one place to another.

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.

seasonal breeding

breeding is confined to a particular season

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.

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.

visual

uses sight to communicate

Ref­er­ences

2006. Na­tional Ge­o­graphic Com­plete Birds of North Amer­ica. Wash­ing­ton, D.C.: Na­tional Ge­o­graphic So­ci­ety.

Ehrlich, P., D. Dobkin, D. Wheye. 1988. The Birder's Hand­book: A Field Guide to the Nat­ural His­tory of North Amer­i­can Birds. New York, NY: Simon and Schus­ter.

Ficken, M. 1962. Ag­o­nis­tic be­hav­ior and ter­ri­tory in the Amer­i­can Red­start. The Auk, 79: 607-632.

Ficken, M. 1963. Courtship of the Amer­i­can Red­start. The Auk, 80: 307-317.

Ger­main, R., M. Reudink, P. Marra, L. Rat­cliffe. 2010. Carotenoid-based Male Plumage Pre­dicts Parental In­vest­ment in the Amer­i­can Red­start. The Wil­son Jour­nal of Or­nithol­ogy, 122/2: 318-325.

Marra, P., R. Holmes. 2001. Con­se­quences of dom­i­nance-me­di­ated habi­tat seg­re­ga­tion in Amer­i­can red­starts dur­ing the non­breed­ing sea­son. The Auk, 118/1: 92-104.

Mc­Cal­lum, C., S. Han­non. 2001. Ac­cip­iter pre­da­tion of Amer­i­can red­start nestlings. The Con­dor, 103/1: 192-194.

Sherry, T., R. Holmes. 1997. "Amer­i­can Red­start (Se­tophaga ru­ti­cilla)" (On-line). The Birds of North Amer­ica On­line. Ac­cessed June 13, 2011 at http://​bna.​birds.​cornell.​edu/​bna/​species/​277.

Sib­ley, D. 2000. The Sib­ley's Guide to Birds. New York: Al­fred A. Knopf, Inc.