Selasphorus rufusrufous hummingbird

Ge­o­graphic Range

Ru­fous hum­ming­birds (Se­las­pho­rus rufus) are mi­gra­tory birds that in­habit the Nearc­tic re­gion. Mi­gra­tory dis­tances av­er­age 2,700 km, but can be as long as 4,000 km. Ru­fous hum­ming­birds travel in a loop pat­tern when mi­grat­ing, rather than a lin­ear path­way.

The breed­ing sea­son lasts from April to July. The hum­ming­birds’ range in­cludes Wash­ing­ton state in the United States north­ward to British Co­lum­bia, Canada. This range is roughly 200 km along the Pa­cific north­west­ern coast of North Amer­ica.

Dur­ing win­ter mi­gra­tion (July-early Sep­tem­ber), the hum­ming­birds travel south­ward through the west­ern US to reach south­ern Cal­i­for­nia and nearly all Mex­ico (ex­cept the south­ern penin­sula). These birds re­main there until late Feb­ru­ary or early March. By March, they travel north­ward along the coast of Cal­i­for­nia to reach Wash­ing­ton again by the end of April. (Healy and Calder, 2006; Supp, et al., 2015)

Habi­tat

In the breed­ing sea­son, ru­fous hum­ming­birds in­habit ter­res­trial habi­tats such as mead­ows, parks, or­chards, conif­er­ous forests, chap­ar­ral and gar­dens. Typ­i­cal areas for these hum­ming­birds are plen­ti­ful with an abun­dance of green plants. The urban areas of Wash­ing­ton state and British Co­lum­bia offer in­clude suit­able habi­tats at high el­e­va­tions and sea­son­ally cool en­vi­ron­ments.

Dur­ing the win­ter, ru­fous hum­ming­birds mi­grate to warmer lo­cales in Mex­ico’s and south­ern Cal­i­for­nia’s moun­tain­ous and wood­land re­gions.

Through­out their range, ru­fous hum­ming­birds live at el­e­va­tions of 1830m to 3000m.

In their mi­gra­tory jour­ney, these hum­ming­birds spend most of their time in the south­west of the US. Be­cause these areas are more desert-like, they are dryer and there­fore do not pro­vide ad­e­quate food sup­ply. (Calder, 1984; Healy and Calder, 2006; Tello-Ramos, et al., 2015)

  • Range elevation
    1830 to 3000 m
    6003.94 to 9842.52 ft

Phys­i­cal De­scrip­tion

Ru­fous hum­ming­birds weigh 2.6-5.7 g (av­er­age 3.4 g). On av­er­age, they are 9.5 cm long with a wingspan of 11.4 cm. There are in­suf­fi­cient data on birth size of these hum­ming­birds. They can have spots of color, but over­all are dull in ap­pear­ance. Males ap­pear to be more col­or­ful than fe­males.

Ru­fous hum­ming­birds have black bills that be­come smoother in adults.

Young birds start with darker skin with­out feath­ers, but have grey strip­ing down ei­ther side of the back. As they grow from hatch­lings to nearly a month old, the feath­ers of the throat re­gion begin to get green with bronze spot­ting. The head be­gins to ap­pear more red or burnt or­ange in color. The fe­males’ throat ap­pear to have more bronze spot­ting and the males’ throat ap­pear or­ange. The fe­males’ throat ap­pear wider than those of males.

In adults, the top of the head down to the nape of the neck is metal­lic bronze-green. This ap­pears duller in fe­males than males. The bronze-green feather color is a theme for most of the body in adults. The face and throat ap­pear more bright red in males and bronze-green in fe­males. Fe­males’ bod­ies have more hints of pur­ple than males.

Subadult hum­ming­birds be­come more rusty red in color, es­pe­cially near the pos­te­rior end of the bird. Feath­ers be­come larger in num­ber on the en­tirety of the bird. Males' tails show metal­lic spot­ting with hints of bronze and green.

Basal meta­bolic rate has been re­ported as 0.0685 W, or 0.018034 W/g. (AnAge, 2014; Healy and Calder, 2006)

  • Sexual Dimorphism
  • sexes colored or patterned differently
  • male more colorful
  • Range mass
    2.6 to 5.7 g
    0.09 to 0.20 oz
  • Average mass
    3.4 g
    0.12 oz
  • Average length
    9.5 cm
    3.74 in
  • Average wingspan
    11.4 cm
    4.49 in
  • Average basal metabolic rate
    0.0685 W cm3.O2/g/hr
  • Average basal metabolic rate
    0.06853 W
    AnAge

Re­pro­duc­tion

Ru­fous hum­ming­birds have a breed­ing sea­son from April to July. Males dive in a “J” mo­tion to at­tract fe­males. After the ini­tial at­trac­tion, mat­ing en­sues on the ground. These ac­tions con­tinue through­out the breed­ing sea­son. These hum­ming­birds are con­sid­ered polyg­y­nous. (Calder, 1973; Healy and Calder, 2006; Hurly, et al., 2001; Tamm, et al., 1989)

These birds have one clutch per year. Eggs are laid be­gin­ning in April with the ma­jor­ity from mid-May until the mid-July. Eggs are laid in nests that are close to the ground and well hid­den in plants and lower branches of trees. These nests, made by fe­males, are made of soft plants and sup­ported by bark, moss and spi­der webs. In gen­eral, the av­er­age clutch size is 2 eggs yearly with an in­cu­ba­tion pe­riod of 15-17 days. Young hum­ming­birds fledge when they are around 15 days old. If the fledg­ing is suc­cess­ful, the hum­ming­birds will not re­turn to the nest and live in­de­pen­dently. There are no data on age of sex­ual ma­tu­rity for ru­fous hum­ming­birds. (Calder, 1973; Cam­field, 2006; Healy and Calder, 2006; Hurly, et al., 2001)

  • Breeding interval
    Rufous hummingbirds breed yearly.
  • Breeding season
    The breeding season for rufous hummingbirds is from April to July.
  • Average eggs per season
    2
  • Average eggs per season
    2
    AnAge
  • Range time to hatching
    15 to 17 days
  • Average fledging age
    15 days
  • Average time to independence
    15 days

In­cu­ba­tion is per­formed by fe­males only. Dur­ing warm weather the fe­male can leave the nest when nec­es­sary for as long as an hour. Fe­males are re­spon­si­ble for their young for as long as they are in the nest. Both par­ents are re­spon­si­ble for feed­ing their off­spring. It’s likely that parental in­volve­ment ceases when the birds reach the fledg­ling stage at 15 days old. (Calder, 1973; Healy and Calder, 2006)

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

Lifes­pan/Longevity

Ru­fous hum­ming­birds, have an av­er­age lifes­pan of 6 years in the wild. Bird band­ing data show the longest liv­ing ru­fous hum­ming­bird to be 8 years and 11 months old. Lifes­pan can be es­ti­mated based on mass of the bird. Ac­cord­ing to Miller and Gass (1985), 3 g hum­ming­birds would have an av­er­age life ex­pectancy of 5.5-5.8 years whereas a 4 g hum­ming­bird would have one of 5.8-6.1 years. There is not suf­fi­cient data for lifes­pan of ru­fous hum­ming­birds in cap­tiv­ity. (Healy and Calder, 2006; Miller and Gass, 1985)

  • Range lifespan
    Status: wild
    8.9 (high) years
  • Average lifespan
    Status: wild
    6 years
  • Average lifespan
    Status: wild
    6 years
  • Average lifespan
    Status: wild
    107 months
    Bird Banding Laboratory

Be­hav­ior

Ru­fous hum­ming­birds are known for their quick, fig­ure-eight move­ment of their wings. This al­lows them to hover as they for­age for food.

These hum­ming­birds are not a so­cial species. Males are highly ter­ri­to­r­ial, not al­low­ing fe­males to share feed­ing grounds dur­ing breed­ing sea­sons. Fe­males feed lower to the ground whereas males hover higher. To keep up with high en­ergy de­mands, the hum­ming­birds must feed con­stantly. To con­serve en­ergy, ru­fous hum­ming­birds can enter a tor­por state. This state is achieved at night­time as well as dur­ing hot days. The big­ger, more en­ergy rich their meals are, the longer tor­por pe­riod they can en­dure. (Healy and Calder, 2006; Tello-Ramos, et al., 2015)

Home Range

There is no in­for­ma­tion on a spe­cific home range for ru­fous hum­ming­birds. ("Cal­i­for­nia Wildlife Habi­tat Re­la­tion­ships Sys­tem", 1988; Healy and Calder, 2006)

Com­mu­ni­ca­tion and Per­cep­tion

Ru­fous hum­ming­birds are not very so­cial, and the ma­jor­ity of sounds they pro­duce are as warn­ing sig­nals. They let out a chip­ping noise to alert oth­ers of dan­ger. In breed­ing, males vi­su­ally at­tract fe­males by a div­ing mo­tion, and do not rely on acoustic mes­sages.

They view the world in color using the UV spec­trum. This is how they make re­ward as­so­ci­a­tions with flow­ers. When mi­grat­ing and for­ag­ing, mem­ory and vi­sual cues are im­por­tant. Spe­cific col­ors, red and yel­low, and lo­ca­tions of flow­ers allow these hum­ming­birds to find re­li­able fuel. (Healy and Calder, 2006)

Food Habits

Ru­fous hum­ming­birds are pri­mar­ily nec­tari­vores but also eat small in­sects. Be­cause they have such a high me­tab­o­lism, they must eat often, eat­ing about half their body weight each day. When they know they will be using a great amount of en­ergy (i.e. mi­grat­ing), they will in­crease their food in­take to ac­com­mo­date those ac­tiv­i­ties. When for­ag­ing for nec­tar, they re­turn where they have had suc­cesses be­fore and use color cues for which flow­ers may sup­ply their next meal. (Cam­field, 2006; Healy and Calder, 2006; Lotz, et al., 2003)

  • Animal Foods
  • insects
  • Plant Foods
  • nectar
  • flowers

Pre­da­tion

Preda­tors prey on hum­ming­birds while hum­ming­birds are hov­er­ing over plants to feed. They are in a more vul­ner­a­ble and un­aware state dur­ing this pe­riod. Pre­da­tion does not play a sig­nif­i­cant role in the mor­tal­ity rate of adult hum­ming­birds.

Ru­fous hum­ming­birds, typ­i­cally males, are known to chase off preda­tors or in­trud­ers to pro­tect their ter­ri­tory. Hum­ming­birds will also make alert sounds to warn oth­ers of im­pos­ing threats. (Cam­field, 2006; Carig­nan, 1988; Healy and Calder, 2006; Wells, 2007)

  • Known Predators
    • No known predators

Ecosys­tem Roles

Ru­fous hum­ming­birds are pol­li­na­tors, which con­tributes to plant re­pro­duc­tion. Haemo­pro­teus archilochus is a pro­to­zoan that uses many ver­te­brates as hosts, in­clud­ing ru­fous hum­ming­birds. This pro­to­zoan at­tacks and de­stroys ery­thro­cytes. Or­nithoica vic­ina and Mi­crolynchia pusilla are species of Hip­po­boscid flies that are par­a­sitic to many birds, in­clud­ing ru­fous hum­ming­birds. These flies are vec­tors to many dis­eases that are harm­ful to birds and mam­mals alike, in­clud­ing malaria. Try­panosoma avium is a par­a­sitic pro­ta­zoan that feeds on the blood and blood mar­row of many bird species, in­clud­ing ru­fous hum­ming­birds. This par­a­site often en­ters the blood­stream of the hum­ming­bird via in­fected hip­po­boscid flies. (Amaya-Mar­quez, 2009; Healy and Calder, 2006; Mc­Clure, 1984; Sta­bler, et al., 1966; Valk­i­u­nas, 2005)

  • Ecosystem Impact
  • pollinates
Com­men­sal/Par­a­sitic Species
  • Pro­to­zoan Haemo­pro­teus archilochus
  • Pro­to­zoan Try­panosoma avium
  • Hip­po­boscid flies

Eco­nomic Im­por­tance for Hu­mans: Pos­i­tive

Ru­fous hum­ming­birds act as pol­li­na­tors. Pol­li­na­tion is a vital re­quire­ment for the growth of many plants and crops. Hu­mans in­di­rectly ben­e­fit from hum­ming­birds’ eco­nomic role when they con­sume foods that have been pol­li­nated. (Alar­con, et al., 2008; Amaya-Mar­quez, 2009; Healy and Calder, 2006)

  • Positive Impacts
  • pollinates crops

Eco­nomic Im­por­tance for Hu­mans: Neg­a­tive

There are no known ad­verse eco­nomic ef­fects of Se­las­pho­rus rufus on hu­mans. (Alar­con, et al., 2008; Amaya-Mar­quez, 2009; Healy and Calder, 2006)

Con­ser­va­tion Sta­tus

Ac­cord­ing to the IUCN Red list, ru­fous hum­ming­birds are listed as a species of “Least Con­cern.” They are pro­tected under the US Mi­gra­tory Bird Act, which pro­hibits the traf­fick­ing and sale of these birds. There is no species sta­tus for the US Fed­eral list or CITES due to large ge­o­graph­i­cal ranges and pop­u­la­tion sizes. Feed­ers cre­ated by hu­mans (Homo sapi­ens) aid hum­ming­birds in win­ter months when food is less read­ily avail­able for them. In re­cent years, the pop­u­la­tions are de­clin­ing, pos­si­bly due to de­for­esta­tion. How­ever, the rate of de­cline does not put the species at risk. Ru­fous hum­ming­birds are being mon­i­tored but no con­ser­va­tion ac­tion plan is cur­rently en­acted. (BirdLife In­ter­na­tional, 2015; Wells, 2007)

Con­trib­u­tors

Car­rie An­der­son (au­thor), Rad­ford Uni­ver­sity, Cari Mc­gre­gor (ed­i­tor), Rad­ford Uni­ver­sity, Zeb Pike (ed­i­tor), Rad­ford Uni­ver­sity, Karen Pow­ers (ed­i­tor), Rad­ford Uni­ver­sity, April Tin­gle (ed­i­tor), Rad­ford Uni­ver­sity, Jacob Vaught (ed­i­tor), Rad­ford Uni­ver­sity, Genevieve Bar­nett (ed­i­tor), Col­orado State Uni­ver­sity.

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

acoustic

uses sound to communicate

agricultural

living in landscapes dominated by human agriculture.

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.

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.

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.

female parental care

parental care is carried out by females

fertilization

union of egg and spermatozoan

forest

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

herbivore

An animal that eats mainly plants or parts of plants.

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).

migratory

makes seasonal movements between breeding and wintering grounds

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.

nectarivore

an animal that mainly eats nectar from flowers

oviparous

reproduction in which eggs are released by the female; development of offspring occurs outside the mother's body.

polygynous

having more than one female as a mate at one time

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

suburban

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

tactile

uses touch to communicate

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

urban

living in cities and large towns, landscapes dominated by human structures and activity.

visual

uses sight to communicate

Ref­er­ences

Cal­i­for­nia De­part­ment of Fish and Wildlife. Cal­i­for­nia Wildlife Habi­tat Re­la­tion­ships Sys­tem. B291. Sacra­mento, CA: Cal­i­for­nia De­part. of Fish and Game. 1988.

Alar­con, R., N. Waser, J. Oller­ton. 2008. Year-to-year vari­a­tion in the topol­ogy of a plant-pol­li­na­tor in­ter­ac­tion net­work. Oikos, 117/12: 1796-1807.

Amaya-Mar­quez, M. 2009. Flo­ral con­stancy in bees: A re­vi­sion of the­o­ries and a com­par­i­son with other pol­li­na­tors. Re­vusta Colom­bri­ana de En­to­molo­gia, 35/2: 206-216.

AnAge, 2014. "AnAge - Me­tab­o­lism" (On-line). AnAge entry for Se­las­pho­rus rufus. Ac­cessed April 19, 2016 at http://​genomics.​senescence.​info/​species/​entry.​php?​species=Selasphorus_​rufus.

BirdLife In­ter­na­tional, 2015. "Se­las­pho­rus rufus" (On-line). The IUCN Red List of Threat­ened Species 2015: e.T22688296A85086092. Ac­cessed Jan­u­ary 27, 2016 at http://​www.​iucnredlist.​org/​details/​summary/​22688296/​0.

Calder, W. 1984. Size, Func­tion and Life His­tory. New York: Courier Cor­per­a­tion.

Calder, W. 1973. The tim­ing of ma­ter­nal be­hav­ior of the broad-tailed hum­ming­bird pre­ced­ing nest fail­ure. The Wil­son Bul­letin, 85/3: 283-290.

Cam­field, A. 2006. Re­source value af­fects ter­ri­to­r­ial de­fense by broad-tailed and ru­fous hum­ming­birds. Jour­nal of Field Or­nithol­ogy, 77/2: 120-125.

Carig­nan, J. 1988. Pre­da­tion on Ru­fous hum­ming­bird by Pray­ing Man­tid. The Texas Jour­nal of Sci­ence, 40/1: 157-158.

Healy, S., W. Calder. 2006. "Ru­fous Hum­ming­bird (Se­las­pho­rus rufus)" (On-line). The Birds of North Amer­ica (A. Poole. Ed.). Ac­cessed Jan­u­ary 24, 2016 at http://​bna.​birds.​cornell.​edu/​bna/​species/​053.

Hurly, T., R. Scott, S. Healy. 2001. The func­tion of dis­plays of male Ru­fous hum­ming­birds. The Con­dor, 103/3: 647-651.

Lasiewski, R. 1964. Body tem­per­a­tures, heart and breath­ing rate, and evap­o­ra­tive water loss in hum­ming­birds. Phys­i­o­log­i­cal Zo­ol­ogy, 37/2: 212-223.

Lotz, C., C. Mar­tinez del Rio, S. Nicol­son. 2003. Hum­ming­birds pay a high cost for a warm drink. Jour­nal of Com­par­a­tive Phys­i­ol­ogy, 173/6: 455-462.

Mc­Clure, H. 1984. The oc­cur­rence of Hip­po­boscid flies on some species of birds in South­ern Cal­i­for­nia. Jour­nal of Field Or­nithol­ogy, 55/2: 230-240.

Miller, R., C. Gass. 1985. Sur­vivor­ship in hum­ming­birds: Is pre­da­tion im­por­tant?. The Auk, 102/1: 175-178.

Nuri Flo­res-Abreu, I., T. Hurly, S. Healy. 2013. Three-di­men­sional spa­tial learn­ing in hum­ming­birds. An­i­mal Be­hav­iour, 85/3: 579-584.

Sta­bler, R., P. Holt, N. Kitzmiller. 1966. Try­panosoma avium in the blood and bone mar­row from 677 Col­orado birds. The Jour­nal of Par­a­sitol­ogy, 52/6: 1141-1144.

Supp, S., F. La Sorte, T. Cormier, M. Lim, D. Pow­ers, S. Wething­ton, S. Goetz, C. Gra­ham. 2015. Cit­i­zen-sci­ence data pro­vides new in­sight into an­nual and sea­sonal vari­a­tion in mi­gra­tion pat­terns. Ecos­phere, 6/1: 15.

Tamm, S., D. Arm­strong, Z. Tooze. 1989. Dis­play be­hav­ior of male cal­liope hum­ming­birds dur­ing the breed­ing sea­son. The Con­dor, 91/2: 272-279.

Tello-Ramos, M., T. Hurly, C. Hig­gott, S. Healy. 2015. Time-place learn­ing in wild, free-liv­ing hum­ming­birds. An­i­mal Be­hav­iour, 104/2015: 123-129.

Valk­i­u­nas, G. 2005. Avian Malaria Par­a­sites and other Haemo­sporidia. Boca Raton: CRC press.

Wells, J. 2007. Birder's Con­ser­va­tion Hand­book: 100 North Amer­i­can Birds at Risk. Prince­ton: Prince­ton Uni­ver­sity Press.