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.
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.
- Habitat Regions
- terrestrial
- Other Habitat Features
- urban
- suburban
- agricultural
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.
- Other Physical Features
- endothermic
- bilateral symmetry
- Sexual Dimorphism
- sexes colored or patterned differently
- male more colorful
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.
- Mating System
- polygynous
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.
- Key Reproductive Features
- iteroparous
- seasonal breeding
- gonochoric/gonochoristic/dioecious (sexes separate)
- sexual
- fertilization
- oviparous
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.
- Parental Investment
- female parental care
-
pre-hatching/birth
-
protecting
- female
-
protecting
-
pre-weaning/fledging
-
provisioning
- female
-
protecting
- male
- female
-
provisioning
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.
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.
- Key Behaviors
- motile
- migratory
- daily torpor
- territorial
Home Range
There is no information on a specific home range for rufous hummingbirds.
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.
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.
- Primary Diet
- herbivore
- 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.
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.
- Ecosystem Impact
- pollinates
- 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.
- Positive Impacts
- pollinates crops
Economic Importance for Humans: Negative
There are no known adverse economic effects of
Selasphorus rufus
on humans.
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.
Additional Links
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.
- 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.
- native range
-
the area in which the animal is naturally found, the region in which it is endemic.
- terrestrial
-
Living on the ground.
- 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.
- forest
-
forest biomes are dominated by trees, otherwise forest biomes can vary widely in amount of precipitation and seasonality.
- mountains
-
This terrestrial biome includes summits of high mountains, either without vegetation or covered by low, tundra-like vegetation.
- urban
-
living in cities and large towns, landscapes dominated by human structures and activity.
- suburban
-
living in residential areas on the outskirts of large cities or towns.
- agricultural
-
living in landscapes dominated by human agriculture.
- polygynous
-
having more than one female as a mate at one time
- 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).
- 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
- fertilization
-
union of egg and spermatozoan
- oviparous
-
reproduction in which eggs are released by the female; development of offspring occurs outside the mother's body.
- female parental care
-
parental care is carried out by females
- motile
-
having the capacity to move from one place to another.
- migratory
-
makes seasonal movements between breeding and wintering grounds
- 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
- visual
-
uses sight to communicate
- acoustic
-
uses sound to communicate
- visual
-
uses sight to communicate
- tactile
-
uses touch to communicate
- acoustic
-
uses sound to communicate
- chemical
-
uses smells or other chemicals to communicate
- herbivore
-
An animal that eats mainly plants or parts of plants.
- nectarivore
-
an animal that mainly eats nectar from flowers
- 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.
- 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.
References
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.
California Department of Fish and Wildlife. California Wildlife Habitat Relationships System. B291. Sacramento, CA: California Depart. of Fish and Game. 1988.