Temporal range: Rupelian to present
|Female black-chinned hummingbird|
For an alphabetic species list, see:
Hummingbirds are New World birds that constitute the family Trochilidae. They are among the smallest of birds, most species measuring 7.5–13 cm (3–5 in). Indeed, the smallest extant bird species is a hummingbird, the 5-cm bee hummingbird weighing less than a U.S. penny (2.5 g).
They are known as hummingbirds because of the humming sound created by their beating wings which flap at high frequencies audible to humans. They hover in mid-air at rapid wing-flapping rates, typically around 50 times per second, allowing them also to fly at speeds exceeding 15 m/s (54 km/h; 34 mph).
Hummingbirds have the highest metabolism of any homeothermic animal. To conserve energy when food is scarce, and nightly when not foraging, they go into torpor, a state similar to hibernation, slowing metabolic rate to 1/15th of its normal rate.
A map of the hummingbird family tree—reconstructed from analysis of 284 of the world's 338 known species—shows rapid diversification from 22 million years ago. Hummingbirds fall into nine main clades, the Topazes, Hermits, Mangoes, Brilliants, Coquettes, Patagona, Mountain Gems, Bees, and Emeralds, defining their relationship to nectar-bearing flowering plants and the birds' continued spread into new geographic areas.
While all hummingbirds depend on flower nectar to fuel their high metabolisms and hovering flight, coordinated changes in flower- and bill shape stimulated the formation of new species of hummingbirds and plants. Due to this exceptional evolutionary pattern, as many as 140 hummingbird species can coexist in a specific region, such as the Andes Mountains.
The hummingbird evolutionary tree shows ancestral hummingbirds splitting from insectivorous swifts (family Apodidae) and treeswifts (family Hemiprocnidae) about 42 million years ago, probably in Eurasia. One key evolutionary factor appears to be an altered taste receptor that enabled hummingbirds to seek nectar. By 22 million years ago the ancestral species of current hummingbirds became established in South America, where environmental conditions stimulated further diversification.
The Andes Mountains appear to be a particularly rich environment for hummingbird evolution because diversification occurred simultaneously with mountain uplift over the past 10 million years. Hummingbirds remain in dynamic diversification inhabiting ecological regions across South America, North America, and the Caribbean, indicating an enlarging evolutionary radiation.
Within the same geographic region, hummingbird clades co-evolved with nectar-bearing plant clades, affecting mechanisms of pollination. The same is true for the sword-billed hummingbird (Ensifera ensifera), one of the morphologically most extreme species, and one of its main food plant clades (Passiflora section Tacsonia).
Hummingbirds exhibit sexual size dimorphism according to Rensch's rule, in which males are smaller than females in small species, and males are larger than females in large-bodied species. The extent of this sexual size difference varies among clades of hummingbirds. For example, the Mellisugini clade exhibits a large size dimorphism, with females being larger than males. Conversely, the Lophomithini clade displays very little size dimorphism; males and females are similar in size. Sexual dimorphisms in beak size and shape are also present between male and female hummingbirds, where in many clades, females have longer, more curved beaks favored for accessing nectar from tall flowers. For males and females of the same size, females will tend to have larger beaks.
Sexual size and beak differences likely evolved due to constraints imposed by courtship because mating displays of male hummingbirds require complex aerial maneuvers and are costly in terms of energy. Males tend to be smaller than females, allowing conservation of energy to forage competitively and participate more frequently in courtship. Thus, sexual selection will favor smaller male hummingbirds.
Female hummingbirds tend to be larger, requiring more energy, and their beaks longer to access preferred flowers. Female hummingbirds tend to have longer beaks that allow for more effective reach into crevices of tall flowers for nectar. Thus females are better at foraging, acquiring flower nectar, and supporting the energy demands of their larger body size. Directional selection will thus favor the larger hummingbirds in terms of acquiring food.
Another evolutionary cause of this sexual bill dimorphism is that the selective forces from competition for nectar between the sexes of each species are what drive the sexual dimorphism. Depending on which sex holds territory in the species, it is advantageous for the other sex to have a longer bill and be able to feed on a wide variety of flowers, decreasing intraspecific competition. For example, in species of hummingbirds where males have longer bills, males do not hold a specific territory and have a lek mating system. In species where males have shorter bills than females, males defend their resources and therefore females must have a longer bill in order to feed from a broader range of flower.
Co-evolution with ornithophilous flowers
Hummingbirds are specialized nectarivores and are tied to the ornithophilous flowers upon which they feed. Some species, especially those with unusual bill shapes such as the sword-billed hummingbird and the sicklebills, are co-evolved with a small number of flower species.
Many plants pollinated by hummingbirds produce flowers in shades of red, orange, and bright pink, though the birds will take nectar from flowers of many colors. Hummingbirds can see wavelengths into the near-ultraviolet, but their flowers do not reflect these wavelengths as many insect-pollinated flowers do. This narrow color spectrum may render hummingbird-pollinated flowers relatively inconspicuous to most insects, thereby reducing nectar robbing. Hummingbird-pollinated flowers also produce relatively weak nectar (averaging 25% sugars w/w) containing a high proportion of sucrose, whereas insect-pollinated flowers typically produce more concentrated nectars dominated by fructose and glucose.
Possible beak evolution
In traditional taxonomy, hummingbirds are placed in the order Apodiformes, which also contains the swifts. However, some taxonomists have separated them into their own order, the Trochiliformes. Hummingbirds' wing bones are hollow and fragile, making fossilization difficult and leaving their evolutionary history poorly documented. Though scientists theorize that hummingbirds originated in South America, where species diversity is greatest, possible ancestors of extant hummingbirds may have lived in parts of Europe to what is southern Russia today.
Between 325 and 340 species of hummingbirds are described, depending on taxonomic viewpoint, divided into two subfamilies, the hermits (subfamily Phaethornithinae, 34 species in six genera), and the typical hummingbirds (subfamily Trochilinae, all the others). However, recent phylogenetic analyses suggest that this division is slightly inaccurate, and that there are nine major clades of hummingbirds: the topazes and jacobins, the hermits, the mangoes, the coquettes, the brilliants, the giant hummingbird (Patagona gigas), the mountain-gems, the bees, and the emeralds. The topazes and jacobins combined have the oldest split with the rest of the hummingbirds. The hummingbird family has the second-greatest number of species of any bird family (after the tyrant flycatchers).
Fossil hummingbirds are known from the Pleistocene of Brazil and the Bahamas; however, neither has yet been scientifically described, and fossils and subfossils of a few extant species are known. Until recently, older fossils had not been securely identifiable as those of hummingbirds.
In 2004, Dr Gerald Mayr of the Senckenberg Museum in Frankfurt am Main identified two 30-million-year-old hummingbird fossils. The fossils of this primitive hummingbird species, named Eurotrochilus inexpectatus ("unexpected European hummingbird"), had been sitting in a museum drawer in Stuttgart; they had been unearthed in a clay pit at Wiesloch–Frauenweiler, south of Heidelberg, Germany, and because it was assumed that hummingbirds never occurred outside the Americas, were not recognized to be hummingbirds until Mayr took a closer look at them.
Fossils of birds not clearly assignable to either hummingbirds or a related, extinct family, the Jungornithidae, have been found at the Messel pit and in the Caucasus, dating from 40–35 mya; this indicates that the split between these two lineages indeed occurred at that date. The areas where these early fossils have been found had a climate quite similar to that of the northern Caribbean or southernmost China during that time. The biggest remaining mystery at the present time is what happened to hummingbirds in the roughly 25 million years between the primitive Eurotrochilus and the modern fossils. The astounding morphological adaptations, the decrease in size, and the dispersal to the Americas and extinction in Eurasia all occurred during this timespan. DNA-DNA hybridization results suggest that the main radiation of South American hummingbirds took place at least partly in the Miocene, some 12 to 13 million years ago, during the uplifting of the northern Andes.
In 2013, a 50-million-year-old fossil bird unearthed in Wyoming was found to be a predecessor to both hummingbirds and swifts before the groups diverged.
Lists of genera and species
- List of hummingbird genera
- List of hummingbird species, sortable alphabetically by common or binomial name
Specialized characteristics and metabolism
During evolution, hummingbirds have adapted to the navigational needs of visual processing while in rapid flight or hovering by development of an exceptionally dense array of retinal neurons allowing for increased spatial resolution in the lateral and frontal visual fields. Morphological studies showed that neuronal hypertrophy, relatively the largest in any bird, exists in a brain region called the pretectal nucleus lentiformis mesencephali responsible for refining dynamic visual processing while hovering. Hummingbirds are highly sensitive to the direction and orientation of stimuli in their visual fields, responding in any direction by a change in body position to orient the head and eyes. Hummingbird sensitivity to even minimal motion in the visual field establishes an advantage to precisely hover in place while in complex and dynamic natural environments.
With the exception of insects, hummingbirds while in flight have the highest metabolism of all animals – a necessity to support the rapid beating of their wings during hovering and fast forward flight. Their heart rate can reach as high as 1,260 beats per minute, a rate once measured in a blue-throated hummingbird, with a breathing rate of 250 breaths per minute, even at rest. During flight, oxygen consumption per gram of muscle tissue in a hummingbird is about 10 times higher than that measured in elite human athletes.
Hummingbirds are rare among vertebrates in their ability to rapidly make use of ingested sugars to fuel energetically expensive hovering flight, powering up to 100% of their metabolic needs with the sugars they drink (in comparison, human athletes max out at around 30%). Hummingbirds can use newly ingested sugars to fuel hovering flight within 30–45 minutes of consumption. These data suggest that hummingbirds are able to oxidize sugar in flight muscles at rates high enough to satisfy their extreme metabolic demands. By relying on newly ingested sugars to fuel flight, hummingbirds can reserve their limited fat stores to sustain their overnight fasting or to power migratory flights.
Studies of hummingbirds' metabolisms are relevant to the question of how a migrating ruby-throated hummingbird can cross 800 km (500 mi) of the Gulf of Mexico on a nonstop flight. This hummingbird, like other birds preparing to migrate, stores fat as a fuel reserve, thereby augmenting its weight by as much as 100%, hence increasing potential flying time over open water.
The dynamic range of metabolic rates in hummingbirds requires a parallel dynamic range in kidney function. During a day of nectar consumption with corresponding high water intake that may total five times the body weight per day, hummingbird kidneys process water via glomerular filtration rates (GFR) in amounts proportional to water consumption, thereby avoiding overhydration. During brief periods of water deprivation, however, such as in nighttime torpor, GFR ceases, preserving body water.
Hummingbird kidneys also have a unique ability to control the levels of electrolytes after consuming nectars with high amounts of sodium and chloride or none, indicating that kidney and glomerular structures must be highly specialized for variations in nectar mineral quality. Morphological studies on Anna's hummingbird kidneys showed adaptations of high capillary density in close proximity to nephrons, allowing for precise regulation of water and electrolytes.
During turbulent airflow conditions created experimentally in a wind tunnel, hummingbirds exhibit stable head positions and orientation while hovering at a feeder. When wind gusts from the side, hummingbirds compensate by increasing the amplitude of their wing strokes plane angle and by varying the orientation and enlarging the collective surface area of their tail feathers into the shape of a fan. While hovering, the visual system of a hummingbird separates motions arising from the bird moving through foliage toward an insect or flower for food or from the motion caused by an approaching competitor or predator. In natural settings complex with motion in the visual background, hummingbirds are able to precisely hover in place by rapid coordination of vision with body position.
Song and vocal learning
Consisting of chirps, squeaks, whistles and buzzes, hummingbird songs originate from at least seven specialized nuclei in the forebrain. In a genetic expression study, it was shown that these nuclei enable vocal learning (ability to acquire vocalizations through imitation), a rare trait known to occur in only two other groups of birds (parrots and songbirds) and a few groups of mammals (including humans, whales and dolphins and bats). Within the past 65 million years, only hummingbirds, parrots and songbirds out of 23 bird orders may have independently evolved seven similar forebrain structures for singing and vocal learning, indicating that evolution of these structures is under strong epigenetic constraints possibly derived from a common ancestor.
The blue-throated hummingbird’s song differs from typical oscine songs in its wide frequency range, extending from 1.8 kHz to approximately 30 kHz. It also produces ultrasonic vocalizations which do not function in communication. As blue-throated hummingbirds often alternate singing with catching small ﬂying insects, it is possible the ultrasonic clicks produced during singing disrupt insect ﬂight patterns, making insects more vulnerable to predation.
The metabolism of hummingbirds can slow at night or at any time when food is not readily available: the birds enter a hibernation-like, deep-sleep state (known as torpor) to prevent energy reserves from falling to a critical level. During night-time torpor, body temperature falls from 40 to 18 °C, with heart and breathing rates both slowed dramatically (heart rate to roughly 50 to 180 beats per minute from its daytime rate of higher than 1000).
During torpor, to prevent dehydration, the GFR ceases, preserving needed compounds such as glucose, water, and nutrients. Further, body mass declines throughout nocturnal torpor at a rate of 0.04 g per hour, amounting to about 10% of weight loss each night. The circulating hormone, corticosterone, is one signal that arouses a hummingbird from torpor.
Hummingbirds have long lifespans for organisms with such rapid metabolisms. Though many die during their first year of life, especially in the vulnerable period between hatching and fledging, those that survive may occasionally live a decade or more. Among the better-known North American species, the average lifespan is probably 3 to 5 years. For comparison, the smaller shrews, among the smallest of all mammals, seldom live longer than 2 years. The longest recorded lifespan in the wild relates to a female broad-tailed hummingbird that was banded (ringed) as an adult at least one year old, then recaptured 11 years later, making her at least 12 years old. Other longevity records for banded hummingbirds include an estimated minimum age of 10 years 1 month for a female black-chinned hummingbird similar in size to the broad-tailed hummingbird, and at least 11 years 2 months for a much larger buff-bellied hummingbird.
As far as is known, male hummingbirds do not take part in nesting. Most species build a cup-shaped nest on the branch of a tree or shrub, although a few tropical species normally attach their nests to leaves. The nest varies in size relative to the particular species—from smaller than half a walnut shell to several centimeters in diameter.
Many hummingbird species use spider silk and lichen to bind the nest material together and secure the structure. The unique properties of the silk allow the nest to expand as the young hummingbirds grow. Two white eggs are laid, which despite being the smallest of all bird eggs, are in fact large relative to the adult hummingbird's size. Incubation lasts 14 to 23 days, depending on the species, ambient temperature, and female attentiveness to the nest. The mother feeds her nestlings on small arthropods and nectar by inserting her bill into the open mouth of a nestling, and then regurgitating the food into its crop.
Incubating in Copiapó, Chile
nest with two nestlings in Santa Monica, California
feeding two nestlings in Grand Teton National Park
To serve courtship and territorial competition, many male hummingbirds have plumage with bright, varied coloration resulting both from pigmentation in the feathers and from prism-like cells within the top layers of feathers of the head, gorget, breast, back and wings. When sunlight hits these cells, it is split into wavelengths that reflect to the observer in varying degrees of intensity, with the feather structure acting as a diffraction grating. Iridescent hummingbird colors result from a combination of refraction and pigmentation, since the diffraction structures themselves are made of melanin, a pigment, and may also be colored by carotenoid pigmentation and more subdued black, brown or gray colors dependent on melanin.
By merely shifting position, feather regions of a muted-looking bird can instantly become fiery red or vivid green. In courtship displays for one example, males of the colorful Anna's hummingbird orient their bodies and feathers toward the sun to enhance the display value of iridescent plumage toward a female of interest.
One study of Anna's hummingbirds found that dietary protein was an influential factor in feather color, as birds receiving more protein grew significantly more colorful crown feathers than those fed a low-protein diet. Additionally, birds on a high-protein diet grew yellower (higher hue) green tail feathers than birds on a low-protein diet.
Aerodynamics of flight
Two studies of rufous or Anna's hummingbirds in a wind tunnel used particle image velocimetry techniques to investigate the lift generated on the bird's upstroke and downstroke. The birds produced 75% of their weight support during the downstroke and 25% during the upstroke, with the wings making a "figure 8" motion.
Many earlier studies had assumed that lift was generated equally during the two phases of the wingbeat cycle, as is the case of insects of a similar size. This finding shows that hummingbird hovering is similar to, but distinct from, that of hovering insects such as the hawk moth. Further studies using electromyography in hovering rufous hummingbirds showed that muscle strain in the pectoralis major (principal downstroke muscle) was the lowest yet recorded in a flying bird, and the primary upstroke muscle (supracoracoideus) is proportionately larger than in other bird species. Hummingbird hovering has been estimated to be 20% more efficient than performed by a helicopter drone.
A slow-motion video has shown how the hummingbirds deal with rain when they are flying. To remove the water from their heads, they shake their heads and bodies, similar to a dog shaking, to shed water. Further, when raindrops collectively may weigh as much as 38% of the bird's body weight, hummingbirds shift their bodies and tails horizontally, beat their wings faster, and reduce their wings' angle of motion when flying in heavy rain.
The outer tail feathers of male Anna's (Calypte anna) and Selasphorus hummingbirds (e.g., Allen's, calliope) vibrate during courtship display dives and produce an audible chirp caused by aeroelastic flutter. When courting, the male ascends some 35 meters before diving over an interested female at a speed of 27 m/s, equal to 385 body lengths/second, producing a high-pitched sound. This downward acceleration during a dive is the highest reported for any vertebrate undergoing a voluntary aerial maneuver; in addition to acceleration, the speed, relative to body length, is the largest known for any vertebrate. For instance, it is about twice the diving speed of peregrine falcons in pursuit of prey. At maximum descent speed, about 10 g of gravitational force occurs in the courting hummingbird during a dive. By comparison to humans, this is a g-force acceleration causing near loss of consciousness in fighter pilots during flight of fixed-wing aircraft in a high-speed banked turn.
Hummingbirds cannot make the courtship dive sound when missing their outer tail feathers, and those same feathers could produce the dive-sound in a wind tunnel. The bird can sing at the same frequency as the tail feather chirp, but its small syrinx is not capable of the same volume. The sound is caused by the aerodynamics of rapid air flow past tail feathers, causing them to flutter in a vibration which produces the high-pitched sound of a courtship dive.
Many other species of hummingbirds also produce sounds with their wings or tails while flying, hovering or diving, including the wings of the calliope hummingbird, broad-tailed hummingbird, rufous hummingbird, Allen's hummingbird, and streamertail, as well as the tail of the Costa's hummingbird and the black-chinned hummingbird, and a number of related species. However, the harmonics of sounds during courtship dives vary across species of hummingbirds.
Male rufous and broad-tailed hummingbirds (genus Selasphorus) have a distinctive wing feature during normal flight that sounds like jingling or a buzzing shrill whistle. The trill arises from air rushing through slots created by the tapered tips of the ninth and tenth primary wing feathers, creating a sound loud enough to be detected by female or competitive male hummingbirds and researchers up to 100 m away.
- Announces the sex and presence of a male bird
- Provides audible aggressive defense of feeding territory and an intrusion tactic
- Enhances communication of threat
- Favors mate attraction and courtship
Hummingbirds are restricted to the Americas from south central Alaska to Tierra del Fuego, including the Caribbean. The majority of species occur in tropical and subtropical Central and South America, but several species also breed in temperate climates and some hillstars occur even in alpine Andean highlands at altitudes up to 5,200 metres (17,100 ft).
The greatest species richness is in humid tropical and subtropical forests of the northern Andes and adjacent foothills, but the number of species found in the Atlantic Forest, Central America or southern Mexico also far exceeds the number found in southern South America, the Caribbean islands, the United States, and Canada. While fewer than 25 different species of hummingbirds have been recorded from the United States and fewer than 10 from Canada and Chile each, Colombia alone has more than 160 and the comparably small Ecuador has about 130 species.
The migratory ruby-throated hummingbird breeds in a range from the southeastern United States to Ontario, while the black-chinned hummingbird, its close relative and another migrant, is the most widespread and common species in the southwestern United States. The rufous hummingbird is the most widespread species in western North America.
Most hummingbirds of the U.S. and Canada migrate southward in fall to spend winter in Mexico, the Caribbean Islands, or Central America. A few southern South American species also move north to the tropics during the southern winter. A few species are year-round residents of California and southwestern desert regions of the USA. Among these are Anna's hummingbird, a common resident from southern Arizona and inland California, and buff-bellied hummingbird, an uncommon resident in subtropical woodlands of southern Texas east through the Gulf coast to the Atlantic coast of Florida. Ruby-throated hummingbirds migrate from as far north as Ontario, Canada, in summer, returning to Mexico, South America, southern Texas, and Florida to winter.
The rufous hummingbird breeds farther north than any other species of hummingbird, often breeding in large numbers in temperate western North America and wintering in increasing numbers along the coasts of subtropical Gulf of Mexico and Florida, rather than in western or central Mexico. By migrating in spring as far north as the Yukon or southern Alaska, the rufous hummingbird migrates more extensively and nests farther north than any other hummingbird species, and must tolerate occasional temperatures below freezing in its breeding territory. This cold hardiness enables it to survive temperatures below freezing, provided that adequate shelter and food are available.
As calculated by displacement of body size, the rufous hummingbird makes perhaps the longest migratory journey of any bird in the world. At just over 3 in long, rufous birds travel 3,900-miles one-way from Alaska to Mexico in late summer, a distance equal to 78,470,000 body lengths. By comparison, the 13-inch-long Arctic tern makes a one-way flight of about 11,185 miles, or 51,430,000 body lengths, just 65% of the body displacement during migration by rufous hummingbirds.
The northward migration of rufous hummingbirds occurs along the Pacific flyway and may be time-coordinated with flower and tree leaf emergence in spring in early March, and also with availability of insects as food. Arrival at breeding grounds before nectar availability from mature flowers may jeopardize breeding opportunities, a factor of phenology possibly determining future migratory patterns linked to climate change.
Diet and specializations for food gathering
Hummingbirds drink nectar, a sweet liquid inside certain flowers. Like bees, they are able to assess the amount of sugar in the nectar they eat; they normally reject flower types that produce nectar that is less than 10% sugar and prefer those whose sugar content is higher. Nectar is a mixture of glucose, fructose, and sucrose, and is a poor source of nutrients, so hummingbirds meet their nutritional needs by preying on flying insects and spiders.
Hummingbirds do not spend all day flying, as the energy cost would be prohibitive; the majority of their activity consists simply of sitting or perching. Hummingbirds eat many small meals and consume around half their weight in pure sugar (twice their weight in nectar, if the nectar is 25% sugar) each day. Hummingbirds digest their food rapidly due to their small size and high metabolism; a mean retention time less than an hour has been reported. Hummingbirds spend an average of 10–15% of their time feeding and 75–80% sitting and digesting.
Because they starve so easily, hummingbirds are highly attuned to food sources. Some species, including many found in North America, are territorial and will try to guard food sources (such as a feeder) against other hummingbirds, attempting to ensure a future food supply for itself.
Hummingbird bill shapes vary dramatically, as an adaptation for specialized feeding. Some species, such as hermits (Phaethornis spp.) have long bills that allow them to probe deep into flowers with long corollae. Thornbills have short, sharp bills adapted for feeding from flowers with short corollae and piercing the bases of longer ones. The sicklebills' extremely decurved bills are adapted to extracting nectar from the curved corollae of flowers in the family Gesneriaceae. The bill of the fiery-tailed awlbill has an upturned tip, as in the avocets. The male tooth-billed hummingbird has barracuda-like spikes at the tip of its long, straight bill.
The two halves of a hummingbird's bill have a pronounced overlap, with the lower half (mandible) fitting tightly inside the upper half (maxilla). When a hummingbird feeds on nectar, the bill is usually opened only slightly, allowing the tongue to dart out and into the interior of flowers. Hummingbird bill sizes range from about 5 mm to as long as 100 mm (about 4 in). When catching insects in flight, a hummingbird's jaw flexes downward to widen the gape for successful capture.
Perception of sweet nectar
Perception of sweetness in nectar evolved in hummingbirds during their genetic divergence from insectivorous swifts, their closest bird relatives. Although the only known sweet sensory receptor, called T1R2, is absent in birds, receptor expression studies showed that hummingbirds adapted a carbohydrate receptor identical to the one perceived as umami in humans, essentially repurposing T1R2 to function as a nectar sweetness receptor. This adaptation for taste enabled hummingbirds to detect and exploit sweet nectar as an energy source, facilitating their distribution across geographical regions where nectar-bearing flowers are available.
Tongue as a micropump
Hummingbirds drink with their tongues by rapidly lapping nectar. Their tongues have tubes which run down their lengths and help the hummingbirds drink the nectar. While capillary action was believed to be what drew nectar into these tubes, high-speed photography has revealed that the tubes open down their sides as the tongue goes into the nectar, and then close around the nectar, trapping it so it can be pulled back into the beak. The tongue, which is forked, is compressed until it reaches nectar, then the tongue springs open, the rapid action traps the nectar and the nectar moves up the grooves, like a pump action, with capillary action not involved. Consequently, tongue flexibility enables accessing, transporting and unloading nectar.
Feeders and artificial nectar
In the wild, hummingbirds visit flowers for food, extracting nectar, which is 55% sucrose, 24% glucose and 21% fructose on a dry-matter basis. Hummingbirds also take sugar-water from bird feeders. Such feeders allow people to observe and enjoy hummingbirds up close while providing the birds with a reliable source of energy, especially when flower blossoms are less abundant. A negative aspect of artificial feeders, however, is that the birds may seek less flower nectar for food, so reduce the amount of pollination their feeding naturally provides.
White granulated sugar is the best sweetener to use in hummingbird feeders. A ratio of 1 part sugar to 4 parts water is a common recipe, although hummingbirds will defend feeders more aggressively when sugar content is at 35%, indicating preference for nectar with higher sweetness and sugar content. Brown, turbinado, and "raw" sugars contain iron, which can be deadly to hummingbirds if consumed over long periods. Honey is made by bees from the nectar of flowers, but it is not good to use in feeders because when it is diluted with water, microorganisms easily grow in it, causing it to spoil rapidly.
Red food dye was once thought to be a favorable ingredient for homemade solutions, but is potentially toxic to the birds which are attracted to red flower petals rather than the nectar color. Commercial products sold as "instant nectar" or "hummingbird food" may also contain preservatives and/or artificial flavors as well as dyes, and are not necessary, although the long-term effects of these additives on hummingbirds have not been systematically studied. Although some commercial products contain small amounts of nutritional additives, hummingbirds obtain all necessary nutrients from the insects they eat, rendering added nutrients unnecessary.
Other animals also visit hummingbird feeders. Bees, wasps, and ants are attracted to the sugar-water and may crawl into the feeder, where they may become trapped and drown. Orioles, woodpeckers, bananaquits, raccoons and other larger animals are known to drink from hummingbird feeders, sometimes tipping them and draining the liquid. In the southwestern United States, two species of nectar-drinking bats (Leptonycteris yerbabuenae and Choeronycteris mexicana) visit hummingbird feeders to supplement their natural diet of nectar and pollen from saguaro cacti and agaves.
Superficially similar birds
Some species of sunbirds of Africa, southern and southeastern Asia, and Australia resemble hummingbirds in appearance and behavior, as do perhaps also the honeyeaters of Australia and Pacific islands. These two groups, however, are not related to hummingbirds, as their resemblance is due to convergent evolution.
The hummingbird moth is often mistaken for a hummingbird.
In myth and culture
- Aztecs wore hummingbird talismans, the talismans being representations as well as actual hummingbird fetishes formed from parts of real hummingbirds: emblematic for their vigor, energy, and propensity to do work along with their sharp beaks that mimic instruments of weaponry, bloodletting, penetration, and intimacy. Hummingbird talismans were prized as drawing sexual potency, energy, vigor, and skill at arms and warfare to the wearer.
- The Aztec god of war Huitzilopochtli is often depicted as a hummingbird (right). It was also believed that fallen warriors would return to earth as hummingbirds and butterflies. The Nahuatl word huitzil (hummingbird) is an onomatopoeic word derived from the sounds of the hummingbird's wing-beats and zooming flight.
- One of the Nazca Lines depicts a hummingbird (right).
- Trinidad and Tobago, known as "The land of the hummingbird," displays a hummingbird on that nation's coat of arms, 1-cent coin and emblem of its national airline, Caribbean Airlines (right).
Hummingbirds feeding at 1500fps
Hummingbird feeding from a flower in the University of California Botanical Garden
Hummingbird with yellow pollen on its beak in the University of California Botanical Garden
Juvenile Anna's hummingbird with tongue sticking out
A hummingbird on a feeding fountain in Brazil
Calypte anna perched
Hummingbird attacking larger song sparrow
Hummingbird and honey bee sizes compared
Hummingbird feeding in winter
Hummingbird nesting on a rubber-covered hook
Hummingbird chicks in nest in cactus in Mesa, Arizona
Hummingbird adult in nest in cactus in Mesa, Arizona
A female Anna's Hummingbird perched on a small branch.
Two velvet-purple coronets fighting near a feeding station in the Ecuadorian Chocó cloud forest.
- AeroVironment Nano Hummingbird — artificial hummingbird
- Macroglossum stellatarum — hummingbird hawk-moth
- Hemaris — sphinx moths (hummingbird moths) confused with hummingbirds
- Clark, C. J.; Dudley, R. (2009). "Flight costs of long, sexually selected tails in hummingbirds". Proceedings of the Royal Society B: Biological Sciences. 276 (1664): 2109–2115. doi:10.1098/rspb.2009.0090. PMC 2677254. PMID 19324747.
- Ridgely RS, Greenfield PG (2001). The Birds of Ecuador, Field Guide (1 ed.). Cornell University Press. ISBN 0-8014-8721-8.
- Suarez, R. K. (1992). "Hummingbird flight: Sustaining the highest mass-specific metabolic rates among vertebrates". Experientia. 48 (6): 565–70. doi:10.1007/bf01920240. PMID 1612136.
- "Hummingbirds". Nationalzoo.si.edu. Retrieved 2013-04-01.
- "Hummingbirds' 22-million-year-old history of remarkable change is far from complete". ScienceDaily. 3 April 2014. Retrieved 30 September 2014.
- McGuire, Jimmy A.; Witt, Christopher C.; Altshuler, Douglas L.; Remsen, J. V. (2007-10-01). "Phylogenetic Systematics and Biogeography of Hummingbirds: Bayesian and Maximum Likelihood Analyses of Partitioned Data and Selection of an Appropriate Partitioning Strategy". Systematic Biology. 56 (5): 837–856. doi:10.1080/10635150701656360. ISSN 1063-5157. PMID 17934998.
- McGuire, Jimmy A.; Witt, Christopher C.; Remsen, J. V.; Corl, Ammon; Rabosky, Daniel L.; Altshuler, Douglas L.; Dudley, Robert (Apr 2014). "Molecular Phylogenetics and the Diversification of Hummingbirds". Current Biology. 24 (8): 910–916. doi:10.1016/j.cub.2014.03.016. ISSN 0960-9822. PMID 24704078.
- McGuire, Jimmy A.; Witt, Christopher C.; Jr, J. V. Remsen; Dudley, R.; Altshuler, Douglas L. (2008-08-05). "A higher-level taxonomy for hummingbirds". Journal of Ornithology. 150 (1): 155–165. doi:10.1007/s10336-008-0330-x. ISSN 0021-8375.
- Baldwin, M. W.; Toda, Y.; Nakagita, T.; O'Connell, M. J.; Klasing, K. C.; Misaka, T.; Edwards, S. V.; Liberles, S. D. (2014). "Evolution of sweet taste perception in hummingbirds by transformation of the ancestral umami receptor". Science. 345 (6199): 929–33. doi:10.1126/science.1255097. PMC 4302410. PMID 25146290.
- Abrahamczyk S, Renner SS (2015). "The temporal build-up of hummingbird/plant mutualisms in North America and temperate South America". BMC Evolutionary Biology. 15: 104. doi:10.1186/s12862-015-0388-z.
- Abrahamczyk S, Souto-Vilarós D, McGuire JA, Renner SS (2015). "Diversity and clade ages of West Indian hummingbirds and the largest plant clades dependent on them: a 5–9 Myr young mutualistic system". Biological Journal of the Linnean Society. 114 (4): 848–859. doi:10.1111/bij.12476.
- Abrahamczyk, S.; Souto-Vilaros, D.; Renner, S. S. (2014). "Escape from extreme specialization: Passionflowers, bats and the sword-billed hummingbird". Proceedings of the Royal Society B: Biological Sciences. 281 (1795): 20140888. doi:10.1098/rspb.2014.0888.
- Colwell, Robert K. (2000-11-01). "Rensch's Rule Crosses the Line: Convergent Allometry of Sexual Size Dimorphism in Hummingbirds and Flower Mites". The American Naturalist. 156 (5): 495–510. doi:10.1086/303406. JSTOR 303406.
- Lisle, Stephen P. De; Rowe, Locke (2013-11-01). "Correlated Evolution of Allometry and Sexual Dimorphism across Higher Taxa". The American Naturalist. 182 (5): 630–639. doi:10.1086/673282. JSTOR 673282. PMID 24107370.
- Berns, Chelsea M.; Adams, Dean C. (2012-11-11). "Becoming Different But Staying Alike: Patterns of Sexual Size and Shape Dimorphism in Bills of Hummingbirds". Evolutionary Biology. 40 (2): 246–260. doi:10.1007/s11692-012-9206-3. ISSN 0071-3260.
- Temeles, Ethan J.; Miller, Jill S.; Rifkin, Joanna L. (2010-04-12). "Evolution of sexual dimorphism in bill size and shape of hermit hummingbirds (Phaethornithinae): a role for ecological causation". Philosophical Transactions of the Royal Society of London B: Biological Sciences. 365 (1543): 1053–1063. doi:10.1098/rstb.2009.0284. ISSN 0962-8436. PMC 2830232. PMID 20194168.
- Stiles, Gary (1981). "Geographical Aspects of Bird Flower Coevolution, with Particular Reference to Central America". Annals of the Missouri Botanical Garden. 68 (2): 323–351. doi:10.2307/2398801. JSTOR 2398801.
- Rodríguez-Gironés, M. A.; Santamaría, L. (2004). "Why Are So Many Bird Flowers Red?". PLoS Biol. 2 (10): e350. doi:10.1371/journal.pbio.0020350. PMC 521733. PMID 15486585.
- Altschuler, D. L. (2003). "Flower Color, Hummingbird Pollination, and Habitat Irradiance in Four Neotropical Forests". Biotropica. 35 (3): 344–355. doi:10.1646/02113. JSTOR 30043050.
- Nicolson, S. W. & Fleming, P. A. (2003). "Nectar as food for birds: the physiological consequences of drinking dilute sugar solutions". Plant Syst. Evol. 238: 139–153. doi:10.1007/s00606-003-0276-7.
- Rico-Guevara A, Araya-Salas M (2015). "Bills as daggers? A test for sexually dimorphic weapons in a lekking hummingbird". Behavioral Ecology. 26 (1): 21–29. doi:10.1093/beheco/aru182.
- Mayr, Gerald (March 2005). "Fossil Hummingbirds of the Old World" (PDF). Biologist. 52 (1): 12–16.
- "Oldest hummingbird fossil found". Cbc.ca. 2004-05-06. Retrieved 2009-01-25.
- Bleiweiss, Robert; Kirsch, John A. W.; Matheus, Juan Carlos (1999). "DNA-DNA hybridization evidence for subfamily structure among hummingbirds" (PDF). Auk. 111 (1): 8–19. doi:10.2307/4088500.
- Ksepka, Daniel T.; Clarke, Julia A.; Nesbitt, Sterling J.; Kulp, Felicia B.; Grande, Lance (2013). "Fossil evidence of wing shape in a stem relative of swifts and hummingbirds (Aves, Pan-Apodiformes)". Proceedings of the Royal Society B. 280 (1761): 1761. doi:10.1098/rspb.2013.0580.
- Lisney TJ, Wylie DR, Kolominsky J, Iwaniuk AN (2015). "Eye Morphology and Retinal Topography in Hummingbirds (Trochilidae: Aves)". Brain Behav Evol. 86 (3–4): 176–90. doi:10.1159/000441834. PMID 26587582.
- Iwaniuk AN, Wylie DR (2007). "Neural specialization for hovering in hummingbirds: hypertrophy of the pretectal nucleus Lentiformis mesencephali" (PDF). J Comp Neurol. 500 (2): 211–21. doi:10.1002/cne.21098. PMID 17111358.
- Goller B, Altshuler DL (2014). "Hummingbirds control hovering flight by stabilizing visual motion". Proc Natl Acad Sci U S A. 111 (51): 18375–80. doi:10.1073/pnas.1415975111. PMC 4280641. PMID 25489117.
- Altshuler, D. L.; Dudley, R (2002). "The ecological and evolutionary interface of hummingbird flight physiology". The Journal of Experimental Biology. 205 (Pt 16): 2325–36. PMID 12124359.
- Lasiewski, Robert C. (1964). "Body Temperatures, Heart and Breathing Rate, and Evaporative Water Loss in Hummingbirds". Physiological Zoology. 37 (2): 212–223. doi:10.1086/physzool.37.2.30152332.
- Hargrove, J. L. (2005). "Adipose energy stores, physical work, and the metabolic syndrome: Lessons from hummingbirds". Nutrition Journal. 4: 36. doi:10.1186/1475-2891-4-36. PMC 1325055. PMID 16351726.
- Welch Jr, K. C.; Chen, C. C. (2014). "Sugar flux through the flight muscles of hovering vertebrate nectarivores: A review". Journal of Comparative Physiology B. 184 (8): 945–59. doi:10.1007/s00360-014-0843-y. PMID 25031038.
- Chen, Chris Chin Wah; Welch, Kenneth Collins (2014). "Hummingbirds can fuel expensive hovering flight completely with either exogenous glucose or fructose". Functional Ecology. 28 (3): 589–600. doi:10.1111/1365-2435.12202.
- Welch Jr, K. C.; Suarez, R. K. (2007). "Oxidation rate and turnover of ingested sugar in hovering Anna's (Calypte anna) and rufous (Selasphorus rufus) hummingbirds". Journal of Experimental Biology. 210 (Pt 12): 2154–62. doi:10.1242/jeb.005363. PMID 17562889.
- Skutch, Alexander F. & Singer, Arthur B. (1973). The Life of the Hummingbird. New York: Crown Publishers. ISBN 0-517-50572-X.
- Suarez, R. K.; Gass, C. L. (2002). "Hummingbirds foraging and the relation between bioenergetics and behavior". Comparative Biochemistry and Physiology. Part A. 133 (2): 335–343. doi:10.1016/S1095-6433(02)00165-4. PMID 12208304.
- Bakken, B. H.; McWhorter, T. J.; Tsahar, E.; Martinez del Rio, C. (2004). "Hummingbirds arrest their kidneys at night: diel variation in glomerular filtration rate in Selasphorus platycercus". The Journal of Experimental Biology. 207 (25): 4383–4391. doi:10.1242/jeb.01238. PMID 15557024.
- Bakken, BH; Sabat, P (2006). "Gastrointestinal and renal responses to water intake in the green-backed firecrown (Sephanoides sephanoides), a South American hummingbird". AJP: Regulatory, Integrative and Comparative Physiology. 291 (3): R830–6. doi:10.1152/ajpregu.00137.2006. PMID 16614056.
- Lotz, Chris N.; Martínez Del Rio, Carlos (2004). "The ability of rufous hummingbirds Selasphorus rufus to dilute and concentrate urine". Journal of Avian Biology. 35: 54–62. doi:10.1111/j.0908-8857.2004.03083.x.
- Beuchat CA, Preest MR, Braun EJ (1999). "Glomerular and medullary architecture in the kidney of Anna's Hummingbird". Journal of Morphology. 240 (2): 95–100. doi:10.1002/(sici)1097-4687(199905)240:2<95::aid-jmor1>3.0.co;2-u.
- Ravi S, Crall JD, McNeilly L, Gagliardi SF, Biewener AA, Combes SA (2015). "Hummingbird flight stability and control in freestream turbulent winds". J Exp Biol. 218 (Pt 9): 1444–52. doi:10.1242/jeb.114553. PMID 25767146.
- "Song sounds of various hummingbird species". All About Birds. The Cornell Lab of Ornithology, Cornell University, Ithaca, NY. 2015. Retrieved 25 June 2016.
- Jarvis ED, Ribeiro S, da Silva ML, Ventura D, Vielliard J, Mello CV (2000). "Behaviourally driven gene expression reveals song nuclei in hummingbird brain". Nature. 2000 Aug 10;406(6796):628-32. 406 (6796): 628–32. doi:10.1038/35020570. PMC 2531203. PMID 10949303.
- Gahr M (2000). "Neural song control system of hummingbirds: comparison to swifts, vocal learning (Songbirds) and nonlearning (Suboscines) passerines, and vocal learning (Budgerigars) and nonlearning (Dove, owl, gull, quail, chicken) nonpasserines". J Comp Neurol. 426 (2): 182–96. doi:10.1002/1096-9861(20001016)426:2<182::AID-CNE2>3.0.CO;2-M. PMID 10982462.
- Pytte, C. L.; Ficken, M. S.; Moiseff, A (2004). "Ultrasonic singing by the blue-throated hummingbird: A comparison between production and perception". Journal of Comparative Physiology A. 190 (8): 665–73. doi:10.1007/s00359-004-0525-4. PMID 15164219.
- Hainsworth, F. R.; Wolf, L. L. (1970). "Regulation of oxygen consumption and body temperature during torpor in a hummingbird, Eulampis jugularis". Science. 168 (3929): 368–9. doi:10.1126/science.168.3929.368. PMID 5435893.
- Hiebert, S. M. (1992). "Time-dependent thresholds for torpor initiation in the rufous hummingbird (Selasphorus rufus)". Journal of Comparative Physiology B. 162 (3): 249–55. doi:10.1007/bf00357531. PMID 1613163.
- Hiebert, S. M.; Salvante, K. G.; Ramenofsky, M; Wingfield, J. C. (2000). "Corticosterone and nocturnal torpor in the rufous hummingbird (Selasphorus rufus)". General and Comparative Endocrinology. 120 (2): 220–34. doi:10.1006/gcen.2000.7555. PMID 11078633.
- Powers, D. R.; Brown, A. R.; Van Hook, J. A. (2003). "Influence of normal daytime fat deposition on laboratory measurements of torpor use in territorial versus nonterritorial hummingbirds". Physiological and Biochemical Zoology. 76 (3): 389–97. doi:10.1086/374286. PMID 12905125.
- "The hummingbird project of British Columbia". Rocky Point Bird Observatory, Vancouver Island, British Columbia. 2010. Retrieved 25 June 2016.
- Churchfield, Sara. (1990). The natural history of shrews. Cornell University Press. pp. 35–37. ISBN 0-8014-2595-6.
- Patuxent Wildlife Research Center, Bird Banding Laboratory. Longevity Records AOU Numbers 3930–4920 2009-08-31. Retrieved 2009-09-27.
- Oniki, Y; Willis, E. O. (2000). "Nesting behavior of the swallow-tailed hummingbird, Eupetomena macroura (Trochilidae, Aves)". Brazilian journal of biology = Revista brasleira de biologia. 60 (4): 655–62. doi:10.1590/s0034-71082000000400016. PMID 11241965.
- "Hummingbird nesting (video)". Public Broadcasting System – Nature; from Learner.org, Journey North. 2016. Retrieved 12 May 2016.
- "Hummingbird nesting and fledgling (video)". YouTube. 2011. Retrieved 12 May 2016.
- "Hummingbird Q&A: Nest and eggs". Operation Rubythroat: the Hummingbird Project, Hilton Pond Center for Piedmont Natural History. 2014. Retrieved 21 June 2014.
- "Hummingbird characteristics". learner.org. Annenberg Learner, The Annenberg Foundation. 2015.
- Williamson S (2001). A Field Guide to Hummingbirds of North America. Section: Plumage and Molt. Houghton Mifflin Harcourt. pp. 13–18. ISBN 0-618-02496-4.
- Hamilton WJ (1965). "Sun-oriented display of the Anna's hummingbird" (PDF). The Wilson Bulletin. 77 (1).
- Meadows MG, Roudybush TE, McGraw KJ (2012). "Dietary protein level affects iridescent coloration in Anna's hummingbirds, Calypte anna". J Exp Biol. 215 (16): 2742–50. doi:10.1242/jeb.069351. PMC 3404802. PMID 22837446.
- Rayner, J.M.V. (1995). "Dynamics of vortex wakes of flying and swimming vertebrates". Symp. Soc. Exp. Biol. 49: 131–155. PMID 8571221.
- Warrick DR, Tobalske BW, Powers DR (2005). "Aerodynamics of the hovering hummingbird". Nature. 435 (7045): 1094–7. doi:10.1038/nature03647. PMID 15973407.
- Sapir, N; Dudley, R (2012). "Backward flight in hummingbirds employs unique kinematic adjustments and entails low metabolic cost". Journal of Experimental Biology. 215 (Pt 20): 3603–11. doi:10.1242/jeb.073114. PMID 23014570.
- Tobalske BW, Warrick DR, Clark CJ, Powers DR, Hedrick TL, Hyder GA, Biewener AA (2007). "Three-dimensional kinematics of hummingbird flight". J Exp Biol. 210 (13): 2368–82. doi:10.1242/jeb.005686. PMID 17575042.
- Tobalske, B. W.; Biewener, A. A.; Warrick, D. R.; Hedrick, T. L.; Powers, D. R. (2010). "Effects of flight speed upon muscle activity in hummingbirds". Journal of Experimental Biology. 213 (Pt 14): 2515–23. doi:10.1242/jeb.043844. PMID 20581281.
- Gill V (30 July 2014). "Hummingbirds edge out helicopters in hover contest". BBC News. Retrieved 1 Sep 2014.
- Videler JJ (2005). Avian Flight. Oxford University Press, Ornithology Series. p. 34. ISBN 0-19-856603-4.
- Fernández, M. J.; Dudley, R; Bozinovic, F (2011). "Comparative energetics of the giant hummingbird (Patagona gigas)". Physiological and Biochemical Zoology. 84 (3): 333–40. doi:10.1086/660084. PMID 21527824.
- Morelle R (November 8, 2011). "Hummingbirds shake their heads to deal with rain". BBC News. Retrieved March 22, 2014.
- St. Fleur N (July 20, 2012). "Hummingbird rain trick: New study shows tiny birds alter posture in storms (video)". Huffington Post. Retrieved March 22, 2014.
- Clark, C. J.; Feo, T. J. (2008). "The Anna's hummingbird chirps with its tail: A new mechanism of sonation in birds". Proceedings of the Royal Society B: Biological Sciences. 275 (1637): 955–62. doi:10.1098/rspb.2007.1619. PMC 2599939. PMID 18230592.
- Clark CJ (2014). "Harmonic hopping, and both punctuated and gradual evolution of acoustic characters in Selasphorus hummingbird tail-feathers". PLOS ONE. 9 (4): e93829. doi:10.1371/journal.pone.0093829. PMC 3983109. PMID 24722049.
- Clark, C. J. (2009). "Courtship dives of Anna's hummingbird offer insights into flight performance limits". Proceedings of the Royal Society B: Biological Sciences. 276 (1670): 3047–52. doi:10.1098/rspb.2009.0508. PMC 2817121. PMID 19515669.
- Shender, B. S.; Forster, E. M.; Hrebien, L; Ryoo, H. C.; Cammarota Jr, J. P. (2003). "Acceleration-induced near-loss of consciousness: The "A-LOC" syndrome". Aviation, Space, and Environmental Medicine. 74 (10): 1021–8. PMID 14556561.
- Clark, C. J.; Feo, T. J. (2010). "Why do Calypte hummingbirds "sing" with both their tail and their syrinx? An apparent example of sexual sensory bias". The American Naturalist. 175 (1): 27–37. doi:10.1086/648560. PMID 19916787.
- Clark, C. J.; Elias, D. O.; Prum, R. O. (2013). "Hummingbird feather sounds are produced by aeroelastic flutter, not vortex-induced vibration". Journal of Experimental Biology. 216 (Pt 18): 3395–403. doi:10.1242/jeb.080317. PMID 23737562.
- Clark CJ (2011). "Wing, tail, and vocal contributions to the complex acoustic signals of courting Calliope hummingbirds" (PDF). Current Zoology. 57 (2): 187–196.
- Kovacevic M (2008-01-30). "Hummingbird sings with its tail feathers". Cosmos Magazine. Retrieved 2013-07-13.
- Miller SJ, Inouye DW (1983). "Roles of the Wing Whistle in the Territorial Behaviour of Male Broad-tailed Hummingbirds (Selasphorus platycercus)". Hummingbirds.net, republished from Animal Behavior, 31, 689-700, 1983. Retrieved 13 July 2014.
- Fjeldså, J., & I. Heynen (1999). Genus Oreotrochilus. pp. 623–624 in: del Hoyo, J., A. Elliott, & J. Sargatal. eds. (1999). Handbook of the Birds of the World. Vol. 5. Barn-owls to Hummingbirds. Lynx Edicions, Barcelona. ISBN 84-87334-25-3
- Jaramillo, A., & R. Barros (2010). Species lists of birds for South American countries and territories: Chile.
- Salaman, P., T. Donegan, & D. Caro (2009). Checklist to the Birds of Colombia 2009. Conservation Colombiana 8. Fundación ProAves
- Freile, J. (2009). Species lists of birds for South American countries and territories: Ecuador.
- "The Ontario hummingbird project". The Ontario Hummingbird Project. 2013. Retrieved 3 May 2015.
- Williamson, S. L. (2002). A Field Guide to Hummingbirds of North America (Peterson Field Guide Series). Houghton Mifflin Co., Boston. ISBN 0-618-02496-4
- "The Ontario hummingbird project: migration and range maps". The Ontario Hummingbird Project. 2013. Retrieved March 23, 2014.
- "Rufous Hummingbird". Cornell University Laboratory of Ornithology. 2014. Retrieved 10 April 2014.
- "Hummingbird news: Tracking migration". Journey North, Annenberg Learner, learner.org. Retrieved 22 March 2014.
- McKinney, A. M.; Caradonna, P. J.; Inouye, D. W.; Barr, B; Bertelsen, C. D.; Waser, N. M. (2012). "Asynchronous changes in phenology of migrating Broad-tailed Hummingbirds and their early-season nectar resources". Ecology. 93 (9): 1987–93. doi:10.1890/12-0255.1. PMID 23094369.
- Connor J (15 October 2010). "Not All Sweetness and Light". Cornell University, Laboratory of Ornithology, Allaboutbirds.org, Ithaca, NY.
- Yanega GM, Rubega MA (2004). "Feeding mechanisms: Hummingbird jaw bends to aid insect capture". Nature. 428 (6983): 615. doi:10.1038/428615a. PMID 15071586.
- Unwin, Mike (2011). The Atlas of Birds: Diversity, Behavior, and Conservation. Princeton University Press. p. 57. ISBN 978-1-4008-3825-7.
- Stevens, C. Edward; Hume, Ian D. (2004). Comparative Physiology of the Vertebrate Digestive System. Cambridge University Press. p. 126. ISBN 978-0-521-61714-7.
- Temeles EJ (1996). "A new dimension to hummingbird-flower relationships" (PDF). Oecologia. 105 (4): 517–23. doi:10.1007/bf00330015.
- Baldwin MW, Toda Y, Nakagita T, O'Connell MJ, Klasing KC, Misaka T, Edwards SV, Liberles SD (2014). "Sensory biology. Evolution of sweet taste perception in hummingbirds by transformation of the ancestral umami receptor". Science. 345 (6199): 929–33. doi:10.1126/science.1255097. PMC 4302410. PMID 25146290.
- Li, X (2009). "T1R receptors mediate mammalian sweet and umami taste". Am J Clin Nutr. 90 (3): 733S–737S. doi:10.3945/ajcn.2009.27462G. PMID 19656838.
- Rico-Guevara, Alejandro; Fan, Tai-Hsi; Rubega, Margaret A. (2015-08-22). "Hummingbird tongues are elastic micropumps". Proc. R. Soc. B. 282 (1813): 20151014. doi:10.1098/rspb.2015.1014. ISSN 0962-8452. PMID 26290074.
- Rico-Guevara, A; Rubega, M. A. (2011). "The hummingbird tongue is a fluid trap, not a capillary tube". Proceedings of the National Academy of Sciences. 108 (23): 9356–60. doi:10.1073/pnas.1016944108. PMC 3111265. PMID 21536916.
- Mosher D "High-Speed Video Shows How Hummingbirds Really Drink". Wired.com. May 2, 2011.
- Gorman, James (2015-09-08). "The Hummingbird's Tongue: How It Works". The New York Times. ISSN 0362-4331. Retrieved 2015-09-10.
- Kim, W; Peaudecerf, F; Baldwin, M. W.; Bush, J. W. (2012). "The hummingbird's tongue: A self-assembling capillary syphon". Proceedings of the Royal Society B: Biological Sciences. 279 (1749): 4990–6. doi:10.1098/rspb.2012.1837. PMC 3497234. PMID 23075839.
- Frank, David; Gorman, James (2015-09-08). "ScienceTake | The Hummingbird's Tongue". The New York Times. ISSN 0362-4331. Retrieved 2015-09-10.
- Stahl, J. M.; Nepi, M; Galetto, L; Guimarães, E; Machado, S. R. (2012). "Functional aspects of floral nectar secretion of Ananas ananassoides, an ornithophilous bromeliad from the Brazilian savanna". Annals of Botany. 109 (7): 1243–52. doi:10.1093/aob/mcs053. PMC 3359915. PMID 22455992.
- Avalos, G; Soto, A; Alfaro, W (2012). "Effect of artificial feeders on pollen loads of the hummingbirds of Cerro de la Muerte, Costa Rica". Revista de biologia tropical. 60 (1): 65–73. doi:10.15517/rbt.v60i1.2362. PMID 22458209.
- "Hummingbird Nectar Recipe". Nationalzoo.si.edu. Retrieved 2010-03-20.
- Rousseu, F; Charette, Y; Bélisle, M (2014). "Resource defense and monopolization in a marked population of ruby-throated hummingbirds (Archilochus colubris)". Ecology and Evolution. 4 (6): 776–93. doi:10.1002/ece3.972. PMC 3967903. PMID 24683460.
- "Arizona Veterinary Diagnostic Laboratory Newsletter, April 2005" (PDF). Retrieved 2010-03-20.
- "Feeders and Feeding Hummingbirds (The Entire Article)". Faq.gardenweb.com. 2008-01-09. Retrieved 2009-01-25.
- "Hummingbird F.A.Q.s from the Southeastern Arizona Bird Observatory". Sabo.org. 2008-11-25. Retrieved 2009-01-25.
- Attracting Hummingbirds | Missouri Department of Conservation. Mdc.mo.gov. Retrieved on 2013-04-01.
- Chambers, Lanny (2016). "Please Don't Use Red Dye". Hummingbirds.net. Retrieved 25 June 2016.
- "Should I Add Red Dye to My Hummingbird Food?". Trochilids.com. Retrieved 2010-03-20.
- Williamson, S. (2000). Attracting and Feeding Hummingbirds. (Wild Birds Series) T.F.H. Publications, Neptune City, New Jersey. ISBN 0-7938-3580-1
- "Tucson's Hummingbird Feeder Bats". The Firefly Forest. Retrieved 2010-03-20.
- Prinzinger, R.; Schafer T. & Schuchmann K. L. (1992). "Energy metabolism, respiratory quotient and breathing parameters in two convergent small bird species : the fork-tailed sunbird Aethopyga christinae (Nectariniidae) and the chilean hummingbird Sephanoides sephanoides (Trochilidae)". Journal of Thermal Biology. 17 (2): 71–79. doi:10.1016/0306-4565(92)90001-V.
- Werness, Hope B; Benedict, Joanne H; Thomas, Scott; Ramsay-Lozano, Tiffany (2004). The Continuum Encyclopedia of Animal Symbolism in Art. Continuum International Publishing Group. p. 229. ISBN 978-0-8264-1525-7.
- Fiona MacDonald (2008). How to Be an Aztec Warrior. National Geographic Books. p. 25. ISBN 978-1-4263-0168-1.
- "National Symbols of Trinidad and Tobago". National Library of Trinidad and Tobago, Port of Spain. 2016. Retrieved 18 April 2016.
- "Coins of Trinidad and Tobago". Central Bank of Trinidad and Tobago, Port of Spain. 2015. Retrieved 18 April 2016.
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