Australian zebra finch

Last updated

Australian zebra finch
Taeniopygia guttata - Bushell's Lagoon.jpg
Scientific classification OOjs UI icon edit-ltr.svg
Domain: Eukaryota
Kingdom: Animalia
Phylum: Chordata
Class: Aves
Order: Passeriformes
Family: Estrildidae
Genus: Taeniopygia
Species:
T. castanotis
Binomial name
Taeniopygia castanotis
(Gould, 1837)
Synonyms

Poephila guttata castanotis
Taeniopygia guttata castanotis

Contents

Male in Karratha, Western Australia Taeniopygia guttata -Karratha, Pilbara, Western Australia, Australia -male-8 (2).jpg
Male in Karratha, Western Australia

The Australian zebra finch (Taeniopygia castanotis) [2] is the most common estrildid finch of Central Australia. It ranges over most of the continent, avoiding only the cool humid south and some areas of the tropical far north. The bird has been introduced to Puerto Rico and Portugal. [1] Due to the ease of keeping and breeding the zebra finch in captivity, it has become Australia's most widely studied bird; by 2010, it was the most studied captive model passerine species worldwide, by a considerable margin. [3]

Taxonomy and phylogeny

The Australian zebra finch was described in 1837 by John Gould as Amadina castanotis, about two decades after the Sunda zebra finch (T. guttata) was described. [4] For over a century and a half, the Australian and Sunda zebra finches were classified as a single species, Taeniopygia guttata. They were split by the IUCN Red List and BirdLife International in 2016. The International Ornithological Congress followed suit in 2022 based on studies noting differences in plumage, mtDNA divergence, and assortative mating between both species in captivity. [5] [6]

It is likely that the Australian zebra finch evolved first, with the Sunda zebra finch descending from Australian zebra finches blown out to sea during the Pleistocene. [7]

Habitat and distribution

The Australian zebra finch has the most extensive mainland distribution of the Australian estrilids, being found in about 75% of mainland Australia. The species is generally not found on the coasts, except for the arid western edge. [8]

The Australian zebra finch is generally found in more arid areas. [9] The areas it chooses to occupy are close to water, and places where rain is concentrated after it falls. [10] However, this is likely more related to the abundance of vegetation than the abundance of water as a resource in itself. [11] Within these areas, it is found in grasslands with scattered trees and shrubs, and in open or grassy woodlands. [9] It is also found in cultivated areas, [12] such as rice fields. [13] It usually stays confined to the low coastal areas of the islands it inhabits, but it can move to elevations up to 2,300 metres (7,500 ft) to exploit expanding cultivation and grasslands. [14]

Although Australian zebra finch breeding, for example, is initiated by rainfall, [15] Klaus Immelmann proposed that sustained heavy precipitation is detrimental to the zebra finch. This is supported by the observation that the nest does not shield the chicks or eggs from rain, and rainfall can sometimes result in clutches being abandoned. Furthermore, it is supported by Immelmann's finding that zebra finches left Wyndham after the first heavy rains in November 1959, but returned to breed in April. It is hypothesised that birds in parts of northern Australia migrate inland during the wet season from October to May, and return to the coastal regions during the dryer months. [16]

Life cycle

The life expectancy of an Australian zebra finch is highly variable because of genetic and environmental factors. The zebra finch may reach up to five years in its natural environment. If they are kept caged, they normally live for 5 to 9 years but may live as long as 12 years, [17] with an exceptional case of 14.5 years reported for a caged specimen. [18] The greatest threats to captive zebra finch survival are predation by cats and loss of natural food. [19]

Song and other vocalisations

Australian zebra finches are loud and boisterous singers. Their calls can be a loud beep, meep, oi! or a-ha!. Their song is a few small beeps, leading up to a rhythmic song of varying complexity in males. Each male's song is different, although birds of the same bloodline will exhibit similarities, and all finches will overlay their own uniqueness onto a common rhythmic framework. Due to their extremely fine temporal-auditory discrimination, the zebra finch is able to recognise and respond to micro-auditory details nested within their calls which human ears cannot detect. [20]

Sons generally learn the song of their fathers with little variation. There is a critical sensitive period during which juvenile males learn their songs by imitating a mature, male tutor. [21] Subsong (early, poorly structured vocalisations) evolve into 'plastic song'. This plastic song is variable between renditions but begins to incorporate some recognisable elements of tutor songs. [21] A study conducted by Nottebohm et al., has shown that birds were able to successfully imitate their tutor's song after relatively short exposure (40 playbacks of the motifs lasting 30 seconds total) over the duration of their sensitive learning period. [22] These birds eventually form a "template" of what their correct song should sound like. They rely on auditory feedback for both song learning and practice as juveniles and song maintenance as adults. Adult birds maintain their songs by correcting any deviations from their target song template. During adulthood, by around 90 days, the bird's song goes through a crystallisation phase where their song template is stable and it no longer changes. [21] The learning process can be delayed by exposure to traffic noise. [23]

Male Australian zebra finches begin to sing at puberty, while females lack a singing ability. [17] This is due to a developmental difference, where in the embryo, the male zebra finch produces testosterone, which is transformed into estradiol in the brain, which in turn leads to the development of the nervous system for a song system. [24] There are multiple areas of the brain involved in the production of song. When a bird is singing a learned song, the HVC projects to the robust nucleus of the archistriatum (RA), which itself projects to the hypoglossal motoneurons. These motoneurons control the muscles of the trachea and syrinx. When learning a new song, the HVC sends efferents to Area X in the lobus parolfactorius, which connects to the medial nucleus of the dorsolateral thalamus (DLM). This structure connects to the lateral magnocellular nucleus of the anterior neostriatum (LMAN), which projects to the RA, and continues like a normal learned song would. The function of the various areas involved in learning is still being investigated. [25] Area X is likely involved in the acquisition of a new song, [26] whereas the LMAN likely serves a key role in the plasticity necessary for learning. [25] Activation of song behaviour later depends on androgens. [27]

Because Australian zebra finch males learn their songs from their surroundings, they are often used as avian model organisms to investigate the neural bases of learning, memory, and sensorimotor integration. For example, studies have investigated the role of FoxP2 in song learning and have found that in young finches both knockdown and overexpression of FoxP2 in the striatal song control nucleus, Area X, prevents accurate song learning and tutor imitation. [28] [29] These studies also have implications for human speech. Individuals heterozygous for a point mutation in FOXP2 manifest a speech disorder. [30] Because of similar expression patterns between humans and songbirds, the Australian zebra finch is used as a model to study FoxP2 expression and function. [31] The zebra finch genome was the second bird genome to be sequenced, in 2008, after that of the chicken. [32]

The Australian zebra finch uses an acoustic signal to communicate to embryos. It gives an incubation call to its eggs when the weather is hot—above 26 °C (79 °F)—and when the end of their incubation period is near. This call alters the growth and behaviour of the chicks, with chicks that were given an incubation call having less mass at the end of the nestling phase when they experienced higher nest temperatures. This contrasts with chicks that were not given an incubation call, which have a higher mass at the end of nestling after being exposed to high nest temperatures. Additionally, the chicks called to as an embryo are more likely to call after experiencing high nest temperatures. [33]

Calling behaviour is used by Australian zebra finches to negotiate parental care duties. In an experiment that delayed the return of the males to the nest, it was found that the resulting duets were shorter and calls were made more often. [34] This is the first species that vocal negotiation over parental care has ever been reported. [35]

Behaviour

Breeding

Female with two juveniles in New South Wales, Australia Taeniopygia guttata -Blue Mountains, New South Wales, Australia-8.jpg
Female with two juveniles in New South Wales, Australia
Juvenile zebra finches Zebrafinchchicks.jpg
Juvenile zebra finches

The Australian zebra finch generally breeds in loose colonies of up to 50 nests (although the number of individuals in a colony can be up to about 230 when breeding, and around 350 when not), but it may nest solitarily. It usually places its nest in a thorny shrub poor tree, although it will nest in other structures, natural and artificial. [12] Often, there are multiple nests in one shrub. [9]

In non-arid parts of Australia, colonies are often occupied year-round. [36] During cold days in the non-breeding season, members of these colonies usually feed in flocks for about two hours, breaking up into small groups to rest, preen, sing, and court before foraging again in a large flock until about one hour before sunset, when they return to the colony. On warmer days, some of the small groups return to the colony to build nests and perform their normal activities. During the breeding season, finches finding or building a nest often return after about an hour of feeding, and on cold days they are joined by those incubating or brooding young. Pairs that have not yet laid their eggs sometimes elect to court and mate in special "courting trees" before joining the flock. In the afternoon, most pairs engage in social activities, which often take place at "social trees". [37] The zebra finch frequently does not breed where it was born; of the ringed birds that bred in the Danaher breeding colony ( 36°09′S145°26′E / 36.150°S 145.433°E / -36.150; 145.433 ) from 1985 to 1989, 24% of them were hatched from the colony or in the immediate vicinity. This natal dispersal is not sex-biased, unlike in most passerines. However, males between 36 and 50 days of age are more likely to disperse than females, although after this age, more females disperse than males. [38] Predation is likely a major factor in coloniality; nests in the main colony suffer less predation than nests further away. Pairs with preyed-upon nests are significantly more likely to nest in a bush more than 20 metres (66 ft) away from their previous nesting plant. [39] Another large factor is where others nest: individuals are more likely to nest closer to conspecifics. In addition, reproductive success of conspecifics may play a role in where individuals nest; a study published in 2012 found that this finch was more likely to breed near nests with chicks older than six days (used as a proxy for reproductive success because they fledge about 87% of the time). [40]

The Australian zebra finch builds both a roosting and breeding nest. The former is dome-shaped, has a large entrance on the side, and lacks an entrance tunnel. [41] This nest helps the zebra finch conserve body heat (likely through its roof and walls and by allowing birds to huddle together): an individual in a roosting nest saves about 18% of the energy of one outside. [42] The breeding nest (which generally ranges from about 12 to 24 centimetres (4.7 to 9.4 in) in length [43] ) has a small entrance [41] followed by a tunnel about three to five centimetres (1.2 to 2.0 in) in diameter and up to eight centimetres (3.1 in) in length, which conceals the contents of the nest, leading to the egg chamber, which has (from the outside) a diameter of 12 to 20 centimetres (4.7 to 7.9 in); the latter two are separated by a raised lip, preventing eggs from rolling out. This chamber often sits on an old nest; otherwise, a foundation consisting of many short, stiff stems over horizontal branches is constructed. The walls of the nest range in thickness from one to three centimetres (0.39 to 1.18 in), with an outer layer of longer stiff and rough grass stems and an inner layer of shorter soft and fine stems. The egg chamber is also lined with soft material, such as wool and feathers. [43] Both sites are defended during the day; but while a desperate bird is sometimes let in to the roosting nest during the night, the breeding nest is always guarded. [44]

The Australian zebra finch is an opportunistic breeder, initiating reproductive behaviour about one to three months after water becomes available. This is so that the young hatch when semi-ripe and ripe seeds (their primary food) become available. This finding is in line with the food quality hypothesis of zebra finch breeding, which states that dry grass seed is inadequate as a food source for nestlings, and that higher quality food (like ripening seeds) is needed to sustain them. [15] Thus, in captivity, it can breed year round when provided with sufficient water, [45] and it may attempt to breed several times per breeding season. [46] Zebra finches are socially monogamous, with pair bonds lasting until the death of one of the partners, after which the widowed bird re-pairs. [47] Extra-pair copulation, mating with individuals other than one's mate, occurs occasionally, with females usually soliciting it. [48] Extra-pair parentage is relatively rare in the wild, accounting for about 2% of young. [49] [50] Attempts at forced extra-pair copulations by males occur frequently (about 43.8% of the time in one study); but, females can always successfully resist forced copulations if they so choose. [51]

There are multiple hypotheses as to why extra-pair copulation might have evolved. [52] One theory is the good genes theory, which states that a female chooses extra-pair copulation if the extra-pair male grants its offspring direct benefits as a result of the male's alleles. [53] There are results that seem to support this; a 1992 study found a correlation between the song rate of a male and the attractiveness of it (measured on the basis of how much time the female spent with the male). [48] However, a 2007 study found that the responsiveness of a female (measured by behaviours indicating an intent to copulate or rejection) was not significantly related to the male's beak colour or its song rate. Song rate was instead hypothesised to draw female's attention to males. According to the author, this meant that the validity of the conclusions of the 1992 experiment needed to be reexamined. [51] Combined with the lack of influence that certain morphological traits have, the large control of females over copulation could indicate chase-away sexual selection, [54] where an exaggerated trait is evolved to counter increased resistance by the female to that feature. [55] An additional theory as to why extra-pair copulation might evolve is the between-sex genetic correlation theory. This theory is based on the lack of definite female benefits in extra-pair copulations, and the benefits that males have by being promiscuous. It states that extra-pair mating behaviour could arise from the same set of loci, and thus that strong selection for extra-pair mating behaviour would indirectly select for promiscuous behaviour in females. [52]

There are several traits correlated with increased extra-pair copulations. Spending time with a mate is important; even more important than the attractiveness of a male (as judged by other females; attractiveness as judged by one female was positively correlated with the judgements of other females). [51] Symmetry of both plumage, like chest bands, and artificial features, like leg bands, are preferred by the female, as measured by how often the male is displayed to. [56] Because of the prevalence of extra-pair paternity, males have evolved various mechanisms to try and assure their paternity of a clutch. The male guards its mate by following it and stopping extra-pair copulation attempts. Sperm competition, where two or more males attempt to inseminate a single egg, also occurs. This is indicated by the male in a pair copulating with its mate more often the day before egg-starts. This is because the last male to copulate with a female before the next egg has a 70% to 80% chance of fertilising the egg in question. [57] Another adaptation to sperm competition is the male ejaculating up to seven times more sperm in extra-pair copulations. The increased amount of sperm occurs because of the combination of ejaculate size being controlled by the time between previous copulations, and the fact that extra-pair copulations occur in the male after its period of within-pair copulation period is complete. [58]

The number of eggs ranges from two to eight eggs per clutch, with five being the most common number. [59] These eggs are white or pale greyish blue in colour, and have a size of about 16 by 10 millimetres (0.63 by 0.39 in). They are incubated for 14 to 16 days. [45] From about 5% [49] to 11% of offspring are the result of intraspecific brood parasitism, and in cases of parasitism, there is usually only one parasitic egg per nest. Additionally, parasitised nests often have one more egg than non-parasitised nests. [50] The female may follow a mixed strategy with relation to brood parasitism (being parasitic in addition to incubating its own clutch). From about 32% to 58% of females do this, and almost all (about 96%) lay parasitic eggs before incubating their clutch. Unpaired females sometimes lay parasitic eggs, but paired females do not rely solely on parasitism. A female that parasitised a nest in the past is more likely to do so in the future. Most of these eggs are unsuccessful; that is, the host abandons its otherwise empty nest after a parasitic egg is laid. Additionally, successful parasites are more likely to have future success from parasitism. [46] At least during late incubation, the female zebra finch can distinguish its own eggs on the basis of odour. This method of distinction arises from the visual similarity between parasitic and non-parasitic eggs, and the cost associated with raising an egg other than one's own. [60] When a bird is parasitised during a nesting attempt, it is less likely to be parasitised again during that season and, at the very least, during the next season (although this could be statistical noise). [46]

Young zebra finches fledge about 17 to 18 days after hatching. [9] They feed themselves by around 35 days after hatching, although they are still socially dependent on their parents during this time; the young become socially dependent between 36 and 50 days after hatching. They also develop sexually dimorphic plumage during this period. [38] These finches are quick to attain sexual maturity, [47] with most first attempting to form pair bonds and breed when they get close to 80 days in age. [38] During the second half of the breeding season at the Danaher breeding colony, 44% of pairs attempting to breed were formed by individuals that were born earlier in the season. [47]

Males and females are very similar in size, but are easily distinguished from one another after reaching maturity, as the males usually have bright orange cheek feathers, red beaks (as opposed to the orange beaks of females), and generally more striking black and white patterns. [19]

Inbreeding

Inbreeding causes early death (inbreeding depression) in the zebra finch, although it does not seem to affect fertility. Embryos have a much lower survival rate, with a study finding fertile eggs from sibling pairs had only about a 25% survival rate, compared to about 41% for unrelated pairs. This early difference in survival eventually becomes null after fledging, with about equal survival rates for offspring from both sibling and unrelated pairs. [61] Inbreeding depression mostly arises due to the expression of deleterious recessive alleles. [62]

Diet

The zebra finch primarily eats grass seeds, [13] feeding mostly on semi-ripe and ripe seeds (although it also takes dry seeds [15] ). The seeds are all dehusked, [63] and are found on stems and the ground, with most being taken, at least in the nominate subspecies, from the latter. [9] The grasses they are taken from are commonly between about 1 and 2.6 millimetres (0.039 and 0.102 in) in length, [64] and larger and easily dehusked seeds are preferred. [65] It supplements its diet with insects [9] (mainly ants and termites) caught in short flights from lookout perches, [66] in addition to flowers of the genus Chenopodium . [64] The nestlings diet consists almost entirely of half-ripe [9] and ripe seeds, in addition to green plant material. [15] There are two main reasons why grass seeds are the dietary staple of the zebra finch: they are an abundant and relatively stable food source in this finch's preferred climate, and they are convenient to, for example, dehusk. [67] In some areas, such as the eastern arid zone in Australia, the seeds taken are consistent, whereas in others, like northern Victoria, there are annual changes in the diet, as different species become abundant. [66] The diet of this finch is generally low in species diversity; at Sandringham, Queensland 74% of the seeds eaten over a 15-month period were from Panicum decompositum , for example. [68]

The zebra finch generally forages for seeds on the ground, taking them individually. But, it also eats seeds on the heads of standing grass. To do this, it either flies and pecks out seeds one at a time, or it perches on a nearby branch. It may also take the head to the ground by jumping up and seizing it with its bill or feet. In times of scarcity, the zebra finch can use its bill to dig into the ground to find buried seed. [69] These seeds are generally taken from patches which have fewer husks (when compared to the number of whole seeds) and are larger and more dense. A seed patch may be checked for many months after its supply of seed is depleted. Additionally, colonial roosting and nesting and foraging in flocks can help birds discover new patches of seed. [70]

This bird commonly forages in flocks, although it sometimes forages in pairs or by itself. [13] In the breeding season, small or medium-sized flocks are common, but in the non-breeding season, flocks of up to about 500 birds may be formed. It occasionally forms mixed-species flocks with other estrildids. [9] A feeding flock can be formed by individuals joining those already feeding, or by individuals landing on the ground together. Birds that arrive in this flock later are more likely to rely on scrounging, or taking food from competitors, whereas early arrivals are more likely to find food for themselves. Individuals that tend to explore more may be more dominant (measured by factors such as in what order individuals accessed a food source [71] ), at least in a study that had relatively low food availability and a single source where food could be taken from. These individuals may also be less successful in a scramble competition, where there are multiple points where food can be found. The reason for the latter is hypothesised to be a result of a trade-off between faster speed in sampling an area and lower accuracy in detecting seeds. [72]

Foraging activity in the zebra finch peaks in the first hour after sunrise and the second to last hour before sunset. In the first instance, the increase foraging is generally achieved through many short bouts of foraging, whereas the latter comes from a few long bouts. [73] When food becomes less available, like from August to September in northern Victoria, there is more feeding in the afternoon, less time spent on patches of food before leaving, and the distance between places where food is available is longer. [66] There are generally two groups of individuals based on foraging behaviour. In the first group, the probability of starting or stopping a feeding bout is constant through time, and short meals are more usual. Most birds in this group have longer bouts when the gap between the previous bout is longer. In the second group (which may consist of more birds), the longer a gap is, the more likely the individual is to start feeding again. Additionally, for most birds in this group, the same is true of the stopping of a bout; the longer it is, the more likely it is to be stopped. Feeding is also usually cyclical for the second group. [73]

Drinking and bathing

The Australian zebra finch generally consumes about 24% to 28% of its body weight (or about 3 millilitres (0.11 imp fl oz; 0.10 US fl oz)) in water per day at a temperature of 22 to 23 °C (72 to 73 °F). When at a higher temperature of 40 °C (104 °F), it may drink from 6 to 12 millilitres (0.21 to 0.42 imp fl oz; 0.20 to 0.41 US fl oz) of water per day. The zebra finch also extracts water from seeds, and can get water from metabolising its food. This metabolic water consumption can equal the amount of water that is lost when temperatures are below 23 °C (73 °F), although only for birds that are gradually dehydrated. Suddenly dehydrated birds must be in temperatures below 12 °C (54 °F) before the water lost is equal to that produced by the metabolism. This finch can survive periods of low water consumption; one study that gradually reduced the amount of water given over a period of a few months to just 0.5 to 1 millilitre (0.018 to 0.035 imp fl oz; 0.017 to 0.034 US fl oz) per week at temperatures from 22 to 24 °C (72 to 75 °F) found that the zebra finch could survive these conditions. Additionally, more than half of birds survived in a total water deprivation experiment that ran 513 days long. [11]

When water is close, the Australian zebra finch drinks regularly during the day; if it is over about 5 kilometres (3.1 mi) away, visits generally peak at midday. It prefers to drink from small puddles or other collections of water, especially those with gently sloped banks. Additionally, exposed drinking areas are preferred to more enclosed ones. It can also drink from dew on the tip of leaves. Due to the danger of predation, the zebra finch gathers in flocks in a bush or tree near a waterhole, only going to drink after the group is large enough. It then only drinks for a few seconds. After drinking, the zebra finch generally bathes for around a minute. Then, it dries off and re-oils its plumage in a warm sheltered spot. [11]

The Australian zebra finch needs an average of only 3.6 seconds to drink 1.5 millilitres (0.053 imp fl oz; 0.051 US fl oz) of water. This short amount of time per bout is achieved by this finch's drinking method. It swallows the water it gets while its bill tip is still submerged, unlike most birds that bring their bill tip up to swallow. This unique action is accomplished by having the tongue scoop water into the pharynx. Then, the front of the larynx forces the water into the oesophagus, which, through peristalsis, takes the fluid to the crop. This method could have evolved because the adaptations necessary were already there because of the need to quickly dehusk and swallow seeds. It allows for water to be drunk faster and taken from more diverse sources, such as drops of dew [74] [75] and cattle troughs; the latter requires the bird to drink upside down. [75]

Temperature regulation

The body temperature (as measured from the cloaca ) of the zebra finch may vary from 38 to 44 °C (100 to 111 °F), rising with increasing air temperatures. Body temperatures over 45 °C (113 °F) can cause death within an hour. This finch first cools itself by covering its plumage with water, not moving, and holding its wings out to allow more thinly feathered regions to be exposed. [76] It also has a large capacity for evaporative cooling through the lungs and skin, with measurements of heat lost through evaporative cooling over heat produced being as high as 1.37 at 43.4 °C (110.1 °F). [77] This can occur as a result of panting, which starts to occur when body temperatures reach 42 to 43 °C (108 to 109 °F) (although this may start when the air temperature is as low as 32 °C (90 °F)). This can cause dehydration and may put birds into a lethargic state. [76] Additionally, the zebra finch's simple rete mirabile ophthalmicum (found in the head) makes it unable to cool the brain as effectively as other birds, like the common kestrel. This lacking ability to cool the brain, in combination with dehydration, may cause the mass die-offs found during prolonged periods of high temperatures. [78] For example, in January 1932, temperatures were between 47 and 52 °C (117 and 126 °F) for 16 days in northern Southern Australia, causing upwards of tens of thousands of this bird to die, with many being found in dams. [76] However, so long as drinking water is available, the bird is able to tolerate heat waves on top of the usual high summer temperatures. Tolerance is also achieved through behaviour. In extreme conditions the finch will reduce its activity in the hotter parts of the day, and it is capable of predicting hotter events and will pre-emptively eat and drink in preparation for the hours of enforced inactivity. [79]

Predators

Nest predators of the Australian zebra finch include the tiger snake, brown snake, dragon lizard, pygmy mulga monitor, singing honeyeater, grey-crowned babbler, yellow-throated miner, little crow, Torresian crow, black rat, and house mouse. Carnivorous marsupials are also nest predators, and barn owls take roosting adult zebra finches. [39]

Aviculture

Living space

Zebra finches can be kept in aviaries and cages. [80] They are easy to keep and are suitable even for beginners. The minimum cage dimensions for a pair are around 70 cm × 40 cm × 50 cm (28 in × 16 in × 20 in), with enough horizontal space for flight. The metal bars of the cage should be placed no more than ~1 centimetre (0.39 in) apart. [81] An external aviary should have an indoor space for shelter, where the birds can sleep, rest and hide from bad weather. Because of their social nature they shouldn't be kept alone and should at least be kept in pairs to have company. In addition to providing access to clean, fresh drinking water, zebra finches should have access to a shallow water dish for bathing. [80] [81]

Feeding

The zebra finch diet consists of a seed mixture for small birds. [80] [81] They like different kinds of millet and ears of common cereals and grasses that they can husk themselves. Another important part of their diet are fruits and vegetables, such as apples, cucumbers, grated carrots, bananas, grapes and salad, spinach and other greens. [80] Avocado shouldn't be given due to its toxicity to birds. [80] An important source of minerals is crushed chicken egg shells or cuttlefish bone. [80] [81] Egg food is also recommended. [80] [82]

Nesting

For nesting, it is recommended to provide the birds with a nesting box with the dimensions 15 cm × 15 cm × 15 cm (5.9 in × 5.9 in × 5.9 in) and material for building the nest, such as hay and cotton. If a nest is provided, breeding will typically begin ~1 week after pairing. [83] The female usually lays 5 eggs [59] that are then incubated for 14 - 16 days. [45] Young zebra finches fledge about 17 to 18 days after hatching. [9] They feed themselves by around 35 days after hatching, although they are still socially dependent on their parents during this time; the young become socially independent between 36 and 50 days after hatching. They also develop sexually dimorphic plumage during this period. [38] These finches are quick to attain sexual maturity, with most first attempting to form pair bonds and breed when they get close to 80 days in age. [47]

Health and lifespan in captivity

Zebra finches can have knemicoptes mites, air sac mites, aspergillosis, coccidiosis and blood-sucking mites. [84]

They normally live for 5 to 9 years but may live as long as 12 years or more. [17] [18] This depends on the quality of care, stress, and other factors.

Related Research Articles

<span class="mw-page-title-main">Bird</span> Warm-blooded vertebrates with wings and feathers

Birds are a group of warm-blooded vertebrates constituting the class Aves, characterised by feathers, toothless beaked jaws, the laying of hard-shelled eggs, a high metabolic rate, a four-chambered heart, and a strong yet lightweight skeleton. Birds live worldwide and range in size from the 5.5 cm (2.2 in) bee hummingbird to the 2.8 m common ostrich. There are over 11,000 living species, more than half of which are passerine, or "perching" birds. Birds have wings whose development varies according to species; the only known groups without wings are the extinct moa and elephant birds. Wings, which are modified forelimbs, gave birds the ability to fly, although further evolution has led to the loss of flight in some birds, including ratites, penguins, and diverse endemic island species. The digestive and respiratory systems of birds are also uniquely adapted for flight. Some bird species of aquatic environments, particularly seabirds and some waterbirds, have further evolved for swimming. The study of birds is called ornithology.

<span class="mw-page-title-main">Grey fantail</span> Species of bird

The grey fantail is a small insectivorous bird. There is no sexual dimorphism. It is a common fantail found in Australia, the Solomon Islands, Vanuatu and New Caledonia. The species is considered by many to be conspecific with the New Zealand fantail ; however, differences in its calls lead some authorities to treat it as a separate species. The studies of grey fantail in 1999 by Richard Schodde and Ian Mason recommended that Tasmanian grey fantail was formally classified as R. albiscapa and New Zealand fantails populations as R. fuliginosa

<span class="mw-page-title-main">Tree swallow</span> Species of bird in the Americas

The tree swallow is a migratory bird of the family Hirundinidae. Found in the Americas, the tree swallow was first described in 1807 by French ornithologist Louis Vieillot as Hirundo bicolor. It has since been moved to its current genus, Tachycineta, within which its phylogenetic placement is debated. The tree swallow has glossy blue-green upperparts, with the exception of the blackish wings and tail, and white underparts. The bill is black, the eyes dark brown, and the legs and feet pale brown. The female is generally duller than the male, and the first-year female has mostly brown upperparts, with some blue feathers. Juveniles have brown upperparts, and gray-brown-washed breasts. The tree swallow breeds in the US and Canada. It winters along southern US coasts south, along the Gulf Coast, to Panama and the northwestern coast of South America, and in the West Indies.

<span class="mw-page-title-main">European pied flycatcher</span> Species of bird

The European pied flycatcher is a small passerine bird in the Old World flycatcher family. One of the four species of Western Palearctic black-and-white flycatchers, it hybridizes to a limited extent with the collared flycatcher. It breeds in most of Europe and across the Western Palearctic. It is migratory, wintering mainly in tropical Africa. It usually builds its nests in holes on oak trees. This species practices polygyny, usually bigamy, with the male travelling large distances to acquire a second mate. The male will mate with the secondary female and then return to the primary female in order to help with aspects of child rearing, such as feeding.

<span class="mw-page-title-main">Grasshopper sparrow</span> Species of bird

The grasshopper sparrow is a small New World sparrow. It belongs to the genus Ammodramus, which contains three species that inhabit grasslands and prairies. Grasshopper sparrows are sometimes found in crop fields and they will readily colonize reclaimed grassland. In the core of their range, grasshopper sparrows are dependent upon large areas of grassland where they avoid trees and shrubs. They seek out heterogenous patches of prairie that contain clumps of dead grass or other vegetation where they conceal their nest, and also contain barer ground where they forage for insects, spiders, and seeds. Grasshopper sparrows are unusual among New World sparrows in that they sing two distinct song types, the prevalence of which varies with the nesting cycle. The primary male song, a high trill preceded by a stereotyped series of short chips, is reminiscent of the sounds of grasshoppers and is the origin of this species' name. Like some other birds of the central North American grasslands, this species also moves around a lot, not only via annual migrations, but individuals frequently disperse between breeding attempts or breeding seasons. Grasshopper sparrows are in steep decline across their range, even in the core of the breeding distribution in the tallgrass prairies of the central Great Plains. The Florida grasshopper sparrow is highly endangered.

<span class="mw-page-title-main">Black-throated blue warbler</span> Species of bird

The black-throated blue warbler is a small passerine bird of the New World warbler family. Its breeding ranges are located in the interior of deciduous and mixed coniferous forests in eastern North America. Over the cooler months, it migrates to islands in the Caribbean and Central America. It is very rarely found in western Europe, where it is considered to be a non-indigenous species. The black-throated blue warbler is sexually dimorphic; the adult male has a black face and cheeks, deep blue upperparts and white underparts, while the adult female is olive-brown above and light yellow below.

<span class="mw-page-title-main">Gouldian finch</span> Passerine bird native to Australia

The Gouldian finch, also known as the Gould's finch or the rainbow finch, is a colourful passerine bird that is native to Australia.

<span class="mw-page-title-main">Shiny cowbird</span> Species of bird

The shiny cowbird is a passerine bird in the New World family Icteridae. It breeds in most of South America except for dense forests and areas of high altitude such as mountains. Since 1900 the shiny cowbird's range has shifted northward, and it was recorded in the Caribbean islands as well as the United States, where it is found breeding in southern Florida. It is a bird associated with open habitats, including disturbed land from agriculture and deforestation.

<span class="mw-page-title-main">Australian reed warbler</span> Species of bird

The Australian reed warbler is an Old World warbler in the genus Acrocephalus and is the only Acrocephalus species native to Australia. It has also been observed in Papua New Guinea and nearby islands. The name Acrocephalus refers to the peaked crown found on reed warblers in this genus and can be translated to mean "topmost head" in Greek. The species name australis is translated to mean "southern" in Latin, and refers to the species range, Australia. In its western range the Australian reed warbler is also known as "Koordjikotji" in the local Aboriginal language of Perth and its surrounds.

<span class="mw-page-title-main">Long-tailed paradise whydah</span> Species of bird

The long-tailed paradise whydah or eastern paradise whydah is from the family Viduidae of the order Passeriformes. They are small passerines with short, stubby bills found across Sub-Saharan Africa. They are mostly granivorous and feed on seeds that have ripen and fall on the ground. The ability to distinguish between males and females is quite difficult unless it is breeding season. During this time, the males molt into breeding plumage where they have one distinctive feature which is their long tail. It can grow up to three times longer than its own body or even more. Usually, the whydahs look like ordinary sparrows with short tails during the non-breeding season. In addition, hybridization can occur with these paradise whydahs. Males are able to mimic songs where females can use that to discover their mate. However, there are some cases where females don't use songs to choose their mate but they use either male characteristics like plumages or they can have a shortage of options with song mimicry. Paradise whydahs are brood parasites. They won't destroy the eggs that are originally there but will lay their own eggs in other songbirds nest. Overall, these whydahs are considered least concerned based on the IUCN Red List of threatened species.

Extra-pair copulation (EPC) is a mating behaviour in monogamous species. Monogamy is the practice of having only one sexual partner at any one time, forming a long-term bond and combining efforts to raise offspring together; mating outside this pairing is extra-pair copulation. Across the animal kingdom, extra-pair copulation is common in monogamous species, and only a very few pair-bonded species are thought to be exclusively sexually monogamous. EPC in the animal kingdom has mostly been studied in birds and mammals. Possible benefits of EPC can be investigated within non-human species, such as birds.

<span class="mw-page-title-main">Fairy tern</span> Species of bird

The fairy tern is a small tern which is native to the southwestern Pacific. It is listed as "Vulnerable" by the IUCN and the New Zealand subspecies is "Critically Endangered". Fairy terns live in colonies along the coastlines and estuaries of Australia, New Zealand, and New Caledonia, feeding largely on small, epipelagic schooling fishes, breeding in areas close to their feeding sites. They have a monogamous mating system, forming breeding pairs in which they mate, nest, and care for offspring.

<span class="mw-page-title-main">Rock firefinch</span> Species of bird

The rock firefinch is a species of estrildid finch found in the Jos Plateau of central Nigeria and in Cameroon. It has an estimated global extent of occurrence of 29,000 km2. The rock firefinch was discovered recently, in 1998. Rock firefinches fall in the family Estrildidae, which contains small passerine birds of the Old World and Australasia. Rock firefinches seem to be most closely related to Mali firefinches and Chad firefinches. The species name sanguinodorsalis means blood-red back, which was chosen because it describes the vibrant red back color of the male plumage. The status of the species is evaluated as Least Concern.

<span class="mw-page-title-main">Painted finch</span> Australian bird

The painted finch is a common species of estrildid finch found in Australia. The painted finch acquired its name due to the red and white spotted and mottled underparts of both males and females. The binomial comes from emblema meaning 'mosaic or inlaid work'; and pictum derives from the Latin word pictus, meaning 'painted'. Other names include Emblema finch, mountain finch, painted firetail and Emblema. The painted finch is a popular bird to be kept in captivity and in backyard aviaries.

<span class="mw-page-title-main">Red-eared firetail</span> Species of bird

The red-eared firetail, also known as the boorin, is a small finch-like species of bird. It occurs in dense wetland vegetation of coastal to sub-coastal regions in Southwest Australia. Its appearance is considered appealing, with white spots, black barring and vivid crimson marks at the ear and upper tail. Red-eared firetails are usually only glimpsed briefly, if at all, as they move rapidly and discreetly through their habitat. Most observations occur when their soft voice is heard, or in flight when flushed from the dense scrub. Males and females are similar in colouring and bond as lifelong pairs that occupy a territory centred on their roosting and brooding nest site. The species occupies a similar ecological niche to the beautiful firetail found in the east of Australia, although unlike other species of the genus they only occasionally group together and are almost never seen in large flocks.

A mating call is the auditory signal used by animals to attract mates. It can occur in males or females, but literature is abundantly favored toward researching mating calls in females. In addition, mating calls are often the subject of mate choice, in which the preferences of one gender for a certain type of mating call can drive sexual selection in a species. This can result in sympatric speciation of some animals, where two species diverge from each other while living in the same environment.

<span class="mw-page-title-main">Seabird breeding behavior</span>

The term seabird is used for many families of birds in several orders that spend the majority of their lives at sea. Seabirds make up some, if not all, of the families in the following orders: Procellariiformes, Sphenisciformes, Pelecaniformes, and Charadriiformes. Many seabirds remain at sea for several consecutive years at a time, without ever seeing land. Breeding is the central purpose for seabirds to visit land. The breeding period is usually extremely protracted in many seabirds and may last over a year in some of the larger albatrosses; this is in stark contrast with passerine birds. Seabirds nest in single or mixed-species colonies of varying densities, mainly on offshore islands devoid of terrestrial predators. However, seabirds exhibit many unusual breeding behaviors during all stages of the reproductive cycle that are not extensively reported outside of the primary scientific literature.

<span class="mw-page-title-main">Sexual selection in birds</span> Various types of avian mating rituals/behaviors found in nature

Sexual selection in birds concerns how birds have evolved a variety of mating behaviors, with the peacock tail being perhaps the most famous example of sexual selection and the Fisherian runaway. Commonly occurring sexual dimorphisms such as size and color differences are energetically costly attributes that signal competitive breeding situations. Many types of avian sexual selection have been identified; intersexual selection, also known as female choice; and intrasexual competition, where individuals of the more abundant sex compete with each other for the privilege to mate. Sexually selected traits often evolve to become more pronounced in competitive breeding situations until the trait begins to limit the individual's fitness. Conflicts between an individual fitness and signaling adaptations ensure that sexually selected ornaments such as plumage coloration and courtship behavior are "honest" traits. Signals must be costly to ensure that only good-quality individuals can present these exaggerated sexual ornaments and behaviors.

<span class="mw-page-title-main">Zebra finch</span> Species of finch

The zebra finches are two species of estrildid finch in the genus Taeniopygia found in Australia and Indonesia. They are seed-eaters that travel in large flocks.

<span class="mw-page-title-main">Sunda zebra finch</span> Species of bird

The Sunda zebra finch is a species of bird in the family Estrildidae. It is found in the Lesser Sundas.

References

  1. 1 2 BirdLife International (2018). "Taeniopygia guttata". IUCN Red List of Threatened Species . 2018: e.T103817982A132195948. doi: 10.2305/IUCN.UK.2018-2.RLTS.T103817982A132195948.en . Retrieved 12 November 2021.
  2. ↑ Clayton, N.S.; Birkhead, T. (1989). "Consistency in the scientific name of the zebra finch" (PDF). Auk. 106: 750.
  3. ↑ Griffith, Simon C.; Buchanan, Katherine L. (1 September 2010). "The Zebra Finch: the ultimate Australian supermodel". Emu - Austral Ornithology. 110 (3): v–xii. Bibcode:2010EmuAO.110D...5G. doi:10.1071/MUv110n3_ED. ISSN   0158-4197. S2CID   86055134.
  4. ↑ Zann 1996 , pp. xiii–xiv
  5. ↑ "IOC World Bird List 12.1". IOC World Bird List Datasets. doi:10.14344/ioc.ml.12.1. S2CID   246050277 . Retrieved 29 January 2022.
  6. ↑ Olsson, Urban; Alström, Per (1 May 2020). "A comprehensive phylogeny and taxonomic evaluation of the waxbills (Aves: Estrildidae)". Molecular Phylogenetics and Evolution. 146: 106757. Bibcode:2020MolPE.14606757O. doi: 10.1016/j.ympev.2020.106757 . ISSN   1055-7903. PMID   32028027. S2CID   211048731.
  7. ↑ Zann 1996 , pp. 9–10
  8. ↑ Zann 1996 , p. 19
  9. 1 2 3 4 5 6 7 8 9 Payne, R. (2018). del Hoyo, Josep; Elliott, Andrew; Sargatal, Jordi; Christie, David A.; de Juana, Eduardo (eds.). "Australian Zebra Finch (Taeniopygia castanotis)" . Handbook of the Birds of the World Alive. Barcelona, Spain: Lynx Edicions. doi:10.2173/bow.zebfin2.01. S2CID   216499275 . Retrieved 5 August 2018.
  10. ↑ Zann 1996 , p. 23
  11. 1 2 3 Zann 1996 , pp. 62–68
  12. 1 2 Zann 1996 , p. 27
  13. 1 2 3 Payne, R. (2018). del Hoyo, Josep; Elliott, Andrew; Sargatal, Jordi; Christie, David A.; de Juana, Eduardo (eds.). "Timor Zebra Finch (Taeniopygia guttata)" . Handbook of the Birds of the World Alive. Barcelona, Spain: Lynx Edicions. doi:10.2173/bow.zebfin2.01. S2CID   216499275 . Retrieved 5 August 2018.
  14. ↑ Zann 1996 , p. 17
  15. 1 2 3 4 Zann, Richard A.; Morton, Stephen R.; Jones, Kevin R.; Burley, Nancy T. (1995). "The timing of breeding by zebra finches in relation to rainfall in central Australia". Emu - Austral Ornithology. 95 (3): 208–222. Bibcode:1995EmuAO..95..208Z. doi:10.1071/MU9950208. ISSN   0158-4197.
  16. ↑ Zann 1996 , p. 25
  17. 1 2 3 White, R. & Fraser, A. (2007). "Taeniopygia guttata". Animal Diversity Web. University of Michigan. Retrieved 22 July 2009.
  18. 1 2 "AnAge entry for Taeniopygia guttata". Genomics.senescence.info. Retrieved 25 January 2011.
  19. 1 2 Haddon, Frank (1985). The Golden Book of Australian birds and mammals. Illustrated by Tony Oliver. Golden Press. p. 44. ISBN   978-0-7302-0011-6.
  20. ↑ Dooling, R. J.; Prior, N. H. (2016). "Do we hear what birds hear in birdsong?". Animal Behaviour. 124: 283–289. doi:10.1016/j.anbehav.2016.10.012. PMC   5884127 . PMID   29628517.
  21. 1 2 3 Brainard, Michael S.; Doupe, Allison J. (16 May 2002). "What songbirds teach us about learning". Nature. 417 (6886): 351–358. Bibcode:2002Natur.417..351B. doi:10.1038/417351a. ISSN   0028-0836. PMID   12015616. S2CID   4329603.
  22. ↑ Tchernichovski, Ofer; Lints, Thierry; Mitra, Partha P.; Nottebohm, Fernando (26 October 1999). "Vocal imitation in zebra finches is inversely related to model abundance". Proceedings of the National Academy of Sciences of the United States of America. 96 (22): 12901–12904. Bibcode:1999PNAS...9612901T. doi: 10.1073/pnas.96.22.12901 . ISSN   0027-8424. PMC   23154 . PMID   10536020.
  23. ↑ Brumm, Henrik; Goymann, Wolfgang; Derégnaucourt, Sébastien; Geberzahn, Nicole; Zollinger, Sue Anne (2021). "Traffic noise disrupts vocal development and suppresses immune function". Science Advances. 7 (20): eabe2405. Bibcode:2021SciA....7.2405B. doi: 10.1126/sciadv.abe2405 . PMC   8115921 . PMID   33980481.
  24. ↑ Gahr, M; Konishi, M. (1988). "Developmental changes in estrogen-sensitive neurons in the forebrain of the zebra finch" (PDF). Proceedings of the National Academy of Sciences. 85 (19): 7380–7383. Bibcode:1988PNAS...85.7380G. doi: 10.1073/pnas.85.19.7380 . PMC   282190 . PMID   3174641.
  25. 1 2 Scharff, C; Nottebohm, F (1991). "A comparative study of the behavioral deficits following lesions of various parts of the zebra finch song system: implications for vocal learning". The Journal of Neuroscience. 11 (9): 2896–2913. doi: 10.1523/JNEUROSCI.11-09-02896.1991 . ISSN   0270-6474. PMC   6575264 . PMID   1880555.
  26. ↑ Sohrabji, Farida; Nordeen, Ernest J.; Nordeen, Kathy W. (1990). "Selective impairment of song learning following lesions of a forebrain nucleus in the juvenile zebra finch". Behavioral and Neural Biology. 53 (1): 51–63. doi:10.1016/0163-1047(90)90797-A. ISSN   0163-1047. PMID   2302141.
  27. ↑ Gurney, ME; Konishi, M. (1980). "Hormone-induced sexual differentiation of brain and behavior in zebra finches". Science. 208 (4450): 1380–1383. Bibcode:1980Sci...208.1380G. doi:10.1126/science.208.4450.1380. PMID   17775725. S2CID   11669349.
  28. ↑ Haesler, Sebastian; Rochefort, Christelle; Georgi, Benjamin; Licznerski, Pawel; Osten, Pavel; Scharff, Constance (4 December 2007). "Incomplete and Inaccurate Vocal Imitation after Knockdown of FoxP2 in Songbird Basal Ganglia Nucleus Area X". PLOS Biology. 5 (12): e321. doi: 10.1371/journal.pbio.0050321 . ISSN   1545-7885. PMC   2100148 . PMID   18052609.
  29. ↑ Heston, Jonathan B.; White, Stephanie A. (18 February 2015). "Behavior-linked FoxP2 regulation enables zebra finch vocal learning". The Journal of Neuroscience. 35 (7): 2885–2894. doi:10.1523/JNEUROSCI.3715-14.2015. ISSN   1529-2401. PMC   4331621 . PMID   25698728.
  30. ↑ Lai, Cecilia S. L.; Fisher, Simon E.; Hurst, Jane A.; Vargha-Khadem, Faraneh; Monaco, Anthony P. (4 October 2001). "A forkhead-domain gene is mutated in a severe speech and language disorder". Nature. 413 (6855): 519–523. Bibcode:2001Natur.413..519L. doi:10.1038/35097076. hdl: 11858/00-001M-0000-0012-CB9C-F . ISSN   0028-0836. PMID   11586359. S2CID   4421562.
  31. ↑ Teramitsu, Ikuko; Kudo, Lili C.; London, Sarah E.; Geschwind, Daniel H.; White, Stephanie A. (31 March 2004). "Parallel FoxP1 and FoxP2 Expression in Songbird and Human Brain Predicts Functional Interaction". Journal of Neuroscience. 24 (13): 3152–3163. doi:10.1523/JNEUROSCI.5589-03.2004. ISSN   0270-6474. PMC   6730014 . PMID   15056695.
  32. ↑ Taeniopygia guttata Research Status. Washington University in St. Louis
  33. ↑ Mariette, Mylene M.; Buchanan, Katherine L. (2016). "Prenatal acoustic communication programs offspring for high posthatching temperatures in a songbird". Science. 353 (6301): 812–814. Bibcode:2016Sci...353..812M. doi: 10.1126/science.aaf7049 . PMID   27540172.
  34. ↑ Boucaud, Ingrid CA; Mariette, Mylene M.; Villain, Avelyne S.; Vignal, Clémentine (February 2016). "Vocal negotiation over parental care? Acoustic communication at the nest predicts partners' incubation share". Biological Journal of the Linnean Society . 117 (2): 322–336. doi: 10.1111/bij.12705 . hdl: 10536/DRO/DU:30082281 .
  35. ↑ Izaac, Joshua (2 December 2015). "Zebra finches negotiate parental duties through song". Australian Geographic . Retrieved 5 October 2017.
  36. ↑ Zann 1996 , p. 78
  37. ↑ Zann 1996 , pp. 81–82
  38. 1 2 3 4 Zann, Richard; Runciman, David (2008). "Survivorship, dispersal and sex ratios of zebra finches Taeniopygia guttata in southeast Australia". Ibis. 136 (2): 136–143. doi:10.1111/j.1474-919X.1994.tb01077.x. ISSN   0019-1019.
  39. 1 2 Zann 1996 , p. 76
  40. ↑ Mariette, Mylene M.; Griffith, Simon C. (2012). "Conspecific attraction and nest site selection in a nomadic species, the zebra finch". Oikos. 121 (6): 823–834. Bibcode:2012Oikos.121..823M. doi:10.1111/j.1600-0706.2011.20014.x. ISSN   0030-1299.
  41. 1 2 Kikkawa, Jiro (1980). "Seasonality of nesting by zebra finches at Armidale, NSW". Emu - Austral Ornithology. 80 (1): 13–20. Bibcode:1980EmuAO..80...13K. doi:10.1071/MU9800013. ISSN   0158-4197.
  42. ↑ Zann 1996 , p. 81
  43. 1 2 Zann 1996 , p. 87
  44. ↑ Zann 1996 , p. 73
  45. 1 2 3 Hauber, Mark E. (1 August 2014). The Book of Eggs: A Life-Size Guide to the Eggs of Six Hundred of the World's Bird Species. Chicago: University of Chicago Press. p. 640. ISBN   978-0-226-05781-1.
  46. 1 2 3 Schielzeth, Holger; Bolund, Elisabeth (2010). "Patterns of conspecific brood parasitism in zebra finches". Animal Behaviour. 79 (6): 1329–1337. doi:10.1016/j.anbehav.2010.03.006. ISSN   0003-3472. S2CID   53171704.
  47. 1 2 3 4 Zann 1996 , pp. 84–85
  48. 1 2 Houtman, Anne M. (22 July 1992). "Female Zebra Finches Choose Extra-Pair Copulations with Genetically Attractive Males". Proceedings of the Royal Society B. 249 (1324): 3–6. doi:10.1098/rspb.1992.0075. S2CID   83985353.
  49. 1 2 Griffith, Simon C.; Holleley, Clare E.; Mariette, Mylene M.; Pryke, Sarah R.; Svedin, Nina (2010). "Low level of extrapair parentage in wild zebra finches". Animal Behaviour. 79 (2): 261–264. doi:10.1016/j.anbehav.2009.11.031. ISSN   0003-3472. S2CID   53170552.
  50. 1 2 Birkhead, T. R.; Burke, T.; Zann, R.; Hunter, F. M.; Krupa, A. P. (1990). "Extra-pair paternity and intraspecific brood parasitism in wild zebra finches Taeniopygia guttata, revealed by DNA fingerprinting". Behavioral Ecology and Sociobiology. 27 (5): 315–324. Bibcode:1990BEcoS..27..315B. doi:10.1007/BF00164002. ISSN   0340-5443. S2CID   12744714.
  51. 1 2 3 Forstmeier, Wolfgang (2007). "Do individual females differ intrinsically in their propensity to engage in extra-pair copulations?". PLOS ONE. 2 (9): e952. Bibcode:2007PLoSO...2..952F. doi: 10.1371/journal.pone.0000952 . ISSN   1932-6203. PMC   1978515 . PMID   17895992.
  52. 1 2 Forstmeier, W.; Martin, K.; Bolund, E.; Schielzeth, H.; Kempenaers, B. (2011). "Female extrapair mating behavior can evolve via indirect selection on males". Proceedings of the National Academy of Sciences. 108 (26): 10608–10613. doi: 10.1073/pnas.1103195108 . ISSN   0027-8424. PMC   3127899 . PMID   21670288.
  53. ↑ Forstmeier, Wolfgang; Nakagawa, Shinichi; Griffith, Simon C.; Kempenaers, Bart (2014). "Female extra-pair mating: adaptation or genetic constraint?". Trends in Ecology & Evolution. 29 (8): 456–464. Bibcode:2014TEcoE..29..456F. doi:10.1016/j.tree.2014.05.005. ISSN   0169-5347. PMID   24909948.
  54. ↑ Forstmeier, Wolfgang (2004). "Female resistance to male seduction in zebra finches". Animal Behaviour. 68 (5): 1005–1015. doi:10.1016/j.anbehav.2004.02.003. ISSN   0003-3472. S2CID   53186504.
  55. ↑ Holland, Brett; Rice, William R. (1998). "Perspective: Chase-away sexual selection: Antagonistic seduction versus resistance". Evolution. 52 (1): 1–7. doi: 10.1111/j.1558-5646.1998.tb05132.x . ISSN   0014-3820. PMID   28568154.
  56. ↑ Swaddle, J. P.; Cuthill, I. C. (1994). "Female zebra finches prefer males with symmetric chest plumage". Proceedings of the Royal Society B: Biological Sciences. 258 (1353): 267–271. doi:10.1098/rspb.1994.0172. ISSN   0962-8452. S2CID   85258085.
  57. ↑ Birkhead, T.R.; Hunter, F.M.; Pellatt, J.E. (1989). "Sperm competition in the zebra finch, Taeniopygia guttata". Animal Behaviour. 38 (6): 935–950. doi:10.1016/S0003-3472(89)80135-6. ISSN   0003-3472. S2CID   53168363.
  58. ↑ Birkhead, T. R.; Fletcher, F.; Pellatt, E. J.; Staples, A. (1995). "Ejaculate quality and the success of extra-pair copulations in the zebra finch". Nature. 377 (6548): 422–423. Bibcode:1995Natur.377..422B. doi:10.1038/377422a0. ISSN   0028-0836. S2CID   4263304.
  59. 1 2 Zann 1996 , p. 335
  60. ↑ Moskát, Csaba; Golüke, Sarah; Dörrenberg, Sebastian; Krause, E. Tobias; Caspers, Barbara A. (2016). "Female zebra finches smell their eggs". PLOS ONE. 11 (5): e0155513. Bibcode:2016PLoSO..1155513G. doi: 10.1371/journal.pone.0155513 . ISSN   1932-6203. PMC   4871452 . PMID   27192061.
  61. ↑ Hemmings NL, Slate J, Birkhead TR (2012). "Inbreeding causes early death in a passerine bird". Nature Communications. 3: 863. Bibcode:2012NatCo...3..863H. doi: 10.1038/ncomms1870 . PMID   22643890.
  62. ↑ Charlesworth D, Willis JH (2009). "The genetics of inbreeding depression". Nature Reviews Genetics. 10 (11): 783–96. doi:10.1038/nrg2664. PMID   19834483. S2CID   771357.
  63. ↑ Zann 1996 , p. 45
  64. 1 2 Morton, S. R.; Davies, P. H. (2006). "Food of the zebra finch (Poephila guttata), and an examination of granivory in birds of the Australian arid zone". Australian Journal of Ecology. 8 (3): 235–243. doi:10.1111/j.1442-9993.1983.tb01321.x. ISSN   0307-692X.
  65. ↑ Zann 1996 , pp. 50–51
  66. 1 2 3 Zann 1996 , p. 46
  67. ↑ Zann 1996 , pp. 49–50
  68. ↑ Zann 1996 , p. 48
  69. ↑ Zann 1996 , pp. 51–52
  70. ↑ Zann 1996 , p. 54
  71. ↑ David, Morgan; Auclair, Yannick; Cézilly, Frank (2011). "Personality predicts social dominance in female zebra finches, Taeniopygia guttata, in a feeding context". Animal Behaviour. 81 (1): 219–224. doi:10.1016/j.anbehav.2010.10.008. ISSN   0003-3472. S2CID   53178426.
  72. ↑ David, Morgan; Cézilly, Frank; Giraldeau, Luc-Alain (2011). "Personality affects zebra finch feeding success in a producer–scrounger game". Animal Behaviour. 82 (1): 61–67. doi:10.1016/j.anbehav.2011.03.025. ISSN   0003-3472. S2CID   54412471.
  73. 1 2 Slater, P. J. B. (1974). "The temporal pattern of feeding in the zebra finch". Animal Behaviour. 22 (2): 506–515. doi:10.1016/S0003-3472(74)80050-3. ISSN   0003-3472.
  74. ↑ Zann 1996 , pp. 60–62
  75. 1 2 Heidweiller, J.; Zweers, G. A. (1990). "Drinking mechanisms in the zebra finch and the Bengalese finch". The Condor. 92 (1): 1–28. doi:10.2307/1368379. ISSN   0010-5422. JSTOR   1368379.
  76. 1 2 3 Zann 1996 , pp. 69–71
  77. ↑ Calder, W. A.; King, J. R. (1963). "Evaporative cooling in the zebra finch". Experientia. 19 (11): 603–604. doi:10.1007/BF02151016. ISSN   0014-4754. PMID   14101529. S2CID   22114512.
  78. ↑ Bech, Claus; Midtgård, Uffe (1981). "Brain temperature and the rete mirabile ophthalmicum in the zebra finch (Poephila guttata)". Journal of Comparative Physiology. 145 (1): 89–93. doi:10.1007/BF00782598. ISSN   0174-1578. S2CID   34672423.
  79. ↑ Cooper, Christine Elizabeth; Withers, Philip Carew; Hurley, Laura Leilani; Griffith, Simon Charles (20 November 2019). "The Field Metabolic Rate, Water Turnover, and Feeding and Drinking Behavior of a Small Avian Desert Granivore During a Summer Heatwave". Frontiers in Physiology. 10: 1405. doi: 10.3389/fphys.2019.01405 . PMC   6879461 . PMID   31824330.
  80. 1 2 3 4 5 6 7 "Zebra Finches". Corydon Animal Hospital. 27 February 2019. Retrieved 5 December 2023.
  81. 1 2 3 4 "Zebra finch care | Animal Humane Society". www.animalhumanesociety.org. Retrieved 4 December 2023.
  82. ↑ "Zebra Finch - Taeniopygia guttata or Poephila guttata". www.finchinfo.com. Retrieved 4 December 2023.
  83. ↑ Olson, Christopher R.; Wirthlin, Morgan; Lovell, Peter V.; Mello, Claudio V. (23 October 2014). "Proper Care, Husbandry, and Breeding Guidelines for the Zebra Finch, Taeniopygia guttata". Cold Spring Harbor Protocols. 2014 (12): 1243–1248. doi:10.1101/pdb.prot084780. ISSN   1940-3402. PMC   4574870 . PMID   25342067.
  84. ↑ Myers, Jeannie. "What to Know About the Zebra Finch". WebMD. Retrieved 4 December 2023.

Bibliography

This page is based on this Wikipedia article
Text is available under the CC BY-SA 4.0 license; additional terms may apply.
Images, videos and audio are available under their respective licenses.