Crested auklet | |
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Scientific classification | |
Domain: | Eukaryota |
Kingdom: | Animalia |
Phylum: | Chordata |
Class: | Aves |
Order: | Charadriiformes |
Family: | Alcidae |
Genus: | Aethia |
Species: | A. cristatella |
Binomial name | |
Aethia cristatella (Pallas, 1769) | |
Synonyms | |
Alca cristatella |
The crested auklet (Aethia cristatella) is a small seabird of the family Alcidae, distributed throughout the northern Pacific and the Bering Sea. The species feeds by diving in deep waters, eating krill and a variety of small marine animals. It nests in dense colonies of up to 1 million individuals in the Bering Sea and the Sea of Okhotsk. It often breeds in mixed-species colonies with the least auklet, a smaller congener.
The species is known for its sexual ornaments, found in both males and females. These include colorful plumage with a forehead crest, a striking scent recalling citrus fruit, and a loud trumpet call, all of which appear to have evolved through sexual selection. The total population is around 6 million, almost half in North America. It is in general considered to be of least concern, though the Alaskan population faces additional threats from predation and oil spills.
The crested auklet was first described as Alca cristatella in 1769 by the German zoologist Peter Simon Pallas. [2] The specific epithet cristatella is Neo-Latin for "little crested" from Latin cristatus "crested" or "plumed". [3] It is now placed in the genus Aethia that was introduced by the German naturalist Blasius Merrem in 1788. [4] The genus includes four auklet species. There are no recognised subspecies of the crested auklet. [5] Within the genus. it is most closely related to the whiskered auklet (A. pygmaea). [6] The family Alcidae consists of many species of shorebirds including other auklets (not in the genus Aethia), puffins, razorbills, guillemots, and murres. [7]
The crested auklet can measure 18–27 cm (7.1–10.6 in) in length, 34–50 cm (13–20 in) in wingspan and weigh 195–330 g (6.9–11.6 oz). [8] They have a reddish-orange and yellow tipped bill, yellowish white irises, and white auricular plumes from their eyes to their ears. Their bodies, wings, and tails are primarily dark sooty grey, while their legs and feet are grey and claws black. The males and females are very similar, although the females have slightly smaller and less curved bills, additionally slightly smaller crests. [9]
Crested auklets are known for their forehead crests, which is made of black forward-curving feathers. These forehead crests are highly variable, and can have between two and twenty three narrow forward curving feathers. The average auklet has 12 crest feathers, which are of variable length, between 8.1 and 58.5 millimetres. [10] Auklets have auricular plumes and a bright orange bill with curved accessory plates. [11] Like forehead crests, these features vary widely within auklet populations. [9]
The crested auklet is recognized primarily by two characteristics during the breeding season. The first is its crest, a group of bristle feathers located on top of its head above its eyes. The second is a social odor that the auklets produce during the breeding season, described as smelling like tangerines. This odor originates from tiny wick feathers, located in a small patch of skin between the shoulder blades. [12] In winter plumage, their bills are smaller and dull yellow. They lack accessory plates and their crest and auricular plumes are reduced. [9]
Juveniles are similar to winter adults, but without auricular and crest plumes. Their bills are smaller, and colored a dull brownish yellow. [9] Juveniles take 33 days to reach adult size. [13]
Crested auklets are found throughout the northern Pacific Ocean and Bering Sea. They are particularly prevalent during the non-breeding winter months along the Aleutian Islands, Kuril Islands and the Russian island of Sakhalin. They travel to breeding locations on the islands and shorelines of the Sea of Okhotsk and the Bering Sea during the late spring and summer. [1] Their habitats consist of slopes, boulder fields, lava flows, and sea cliffs. They are often found with other auklet species such as the least auklet. [9] On a daily basis, crested auklets circle 500 meters above the sea and the breeding colonies. This circling is triggered by disturbances and predators posing a threat. [13]
Crested auklets primarily forage in deep waters, however sometimes in areas closer to the shore, but always in large flocks. Little is known about the winter diets, however, it is suggested that they feed on a variety of marine invertebrates. Crested auklets are planktivores. Their diet consists mainly of krill, but they are also known to eat copepods, pteropods (such as Limacina ), amphipods and larval fishes. [9] Crested auklets dive from the surface of the water to catch their food. This behavior has been described as underwater "flight". [14]
The crested auklet breeding season begins mid-May and ends mid-August. [15] Their nesting sites are within the rocky crevices of North Pacific coast. They breed in dense colonies of up to one million birds. Because of this, nesting sites are in close proximity, with as little as 0.3 meters between nests. Even so, there is a high degree of territoriality, and adults show a high degree of site fidelity within a year. [16] Because mating occurs at sea and males have no copulatory organ, males must hover over females for a successful mating. Mate choice is mutual, but females do have final choice on breeding partner. [12]
Crested auklets are highly social during the breeding season, before pair formation, and after pair formation. Within a breeding year, however, crested auklets are monogamous, with only 10% of the population having extra-pair copulations. Partners continue to self-advertise to other birds when they are not incubating. While some of this advertising behavior can be linked to extra-pair mating, it is suggested that continuation of the behavior allows birds to find pairs for the next breeding season. Only 45.5% of birds remain with the same partner in the subsequent breeding season. [12]
Both sexes invest highly in parental care; parents share equally in incubating the single egg and raising the chick. Since both sexes are ornamented, crested auklets align with Robert Trivers's parental investment theory, which predicts that with biparental care, mutual choosiness will arise. [17]
Crested auklets are unique in their use of optical, vocal, and olfactory signals in mating. Their communicative behavior is more complex and diversified than that of closely related species. There are three general evolutionary mechanisms proposed to address the origin of the elaborate display traits of crested auklets, and of showy mating signals by males in general:
Asserted dominance, with regards to claimed display area, has been correlated with crest length in both males and females. The existence of these showy monomorphic traits is indicative of intense sexual selection for both sexes. Large-crested adults of both sexes receive higher levels of sexual interest and displays from the opposite sex compared to those with smaller crests. [10] Crested auklets with larger crests are more likely to obtain mates and to form pair bonds earlier. [10]
Based on divorce rate and mortality, more than half of individuals find a new mate each year. [11] Female crest length is the primary factor of male mate switching between years. [21]
While there is variation in displays across populations, crested auklet crests and plume ornaments are consistent in expression within an individual over time. Furthermore, there is little sexual dimorphism or evidence of condition dependence. From studies, it seems to be a survival-neutral ornament. [15] Some studies, however, offer up a functional purpose for these ornaments. One study suggests a link between habitat complexity and facial feathering, where tactile facial elongation helps individuals navigate complex underground crevices. [22] The high density of crested auklet nesting sites can be expected to impose selective pressures on sensory mechanisms. [22]
Crested auklets have a wide variety of single and complex calls. Billing is "defined as pair courtship with mutual cackling vocal display." It is a crucial part of successful pair formation and becomes harmonious once male and female partners are well acquainted. [12] Trumpet calls are one of the most common advertising calls. The call represents a complex but stereotyped vocal sequence that is linked with a specific visual display. [16] Between individuals, the calls differ in duration and frequency. Calls are primarily performed in males, but can also be seen in females. The call is particularly strong in widowed females. [12] These calls stay stable from year to year, and individuals' specific calls are associated with the maintenance of long-term social bonds between pair mates and between neighbors. This suggests that trumpet calls can be used for both short-term and long-term individual recognition. Recognition of neighboring individuals' calls is advantageous because it minimizes energy expenditure on aggressive displays, and prevents conflict between neighbors and trusted individuals (the "dear enemy phenomenon"). [16]
Crested auklets have a distinctive citrus-like plumage odor. The scent is released when there is ruffling of feathers on the nape and upper back of the individual from threat, trumpeting, or billing displays. The cloud of scent released encourages the ruff sniff display. A ruff sniff display is when birds fully insert their half open bill into the other's plumage. This display occurs in the absence of obvious aggression and is important for pair formation. [12] For both sexes, a strong odor attracts more individuals, which then do a ruff sniff display. [21]
Odor secretions increase during the breeding season, highlighting its association with courtship and mate selection. The scent may also act as an ectoparasite repellent. [23] This scent is also found in whiskered auklet. [13]
According to the International Union for Conservation of Nature, crested auklets are of least concern. [1] The global population exceeds 8.2 million individuals, while the North American population is estimated at 2.9 million birds. However, an accurate assessment of the number of birds is difficult, since those on the surface of the colony and in the nearby sea form only a small proportion of the variable and poorly understood population. [1]
There is greater concern for the Alaskan population. There has been high predation by rats which have escaped from fishing vessels in the harbor. The auklets' main predators are gulls, Arctic fox and common ravens. They have also been reported in the stomachs of halibut caught on St. Lawrence Island. Oil spills and collisions with light sources pose additional risks. In Alaska, there is some subsistence hunting of the species. [14]
Sexual selection is a mechanism of evolution in which members of one biological sex choose mates of the other sex to mate with, and compete with members of the same sex for access to members of the opposite sex. These two forms of selection mean that some individuals have greater reproductive success than others within a population, for example because they are more attractive or prefer more attractive partners to produce offspring. Successful males benefit from frequent mating and monopolizing access to one or more fertile females. Females can maximise the return on the energy they invest in reproduction by selecting and mating with the best males.
Auks or alcids are a group of birds of the family Alcidae in the order Charadriiformes. The alcid family includes the murres, guillemots, auklets, puffins, and murrelets. The family contains 25 extant or recently extinct species that are divided into 11 genera. Auks are found throughout the Northern Hemisphere.
Grouse are a group of birds from the order Galliformes, in the family Phasianidae. Grouse are presently assigned to the tribe Tetraonini, a classification supported by mitochondrial DNA sequence studies, and applied by the American Ornithologists' Union, ITIS, International Ornithological Congress, and others.
Peafowl is a common name for two bird species of the genus Pavo and one species of the closely related genus Afropavo within the tribe Pavonini of the family Phasianidae. Male peafowl are referred to as peacocks, and female peafowl are referred to as peahens.
The pigeon guillemot is a species of bird in the auk family, Alcidae. One of three species in the genus Cepphus, it is most closely related to the spectacled guillemot. There are five subspecies of the pigeon guillemot; all subspecies, when in breeding plumage, are dark brown with a black iridescent sheen and a distinctive wing patch broken by a brown-black wedge. Its non-breeding plumage has mottled grey and black upperparts and white underparts. The long bill is black, as are the claws. The legs, feet, and inside of the mouth are red. It closely resembles the black guillemot, which is slightly smaller and lacks the dark wing wedge present in the pigeon guillemot.
The razorbill is a North Atlantic colonial seabird and the only extant member of the genus Alca of the family Alcidae, the auks. It is the closest living relative of the extinct great auk. Historically, it has also been known as "auk", "razor-billed auk" and "lesser auk".
The "typical" pheasant genus Phasianus in the family Phasianidae consists of two species. The genus name is Latin for pheasant.
The lark bunting is a medium-sized American sparrow native to central and western North America. It was designated the state bird of Colorado in 1931.
The macaroni penguin is a species of penguin found from the Subantarctic to the Antarctic Peninsula. One of six species of crested penguin, it is very closely related to the royal penguin, and some authorities consider the two to be a single species. It bears a distinctive yellow crest on its forehead. Its face and upperparts are black and sharply delineated from the white underparts. Adults weigh on average 5.5 kg (12 lb) and are 70 cm (28 in) in length. The male and female are similar in appearance; the male is slightly larger and stronger with a relatively larger bill. Like all penguins, it is flightless, with a streamlined body and wings stiffened and flattened into flippers for a marine lifestyle.
The parakeet auklet is a small seabird of the North Pacific. Parakeet Auklets used to be placed on its own in the genus Cyclorrhynchus but recent morphological and genetic evidence suggest it should be placed in the genus Aethia, making them closely related to crested auklets and least auklets. It is associated with the boreal waters of Alaska, Kamchatka and Siberia. It breeds on the cliffs, slopes and boulder fields of offshore islands, generally moving south during the winter.
The rhinoceros auklet is a seabird and a close relative of the puffins. It is the only extant species of the genus Cerorhinca. Given its close relationship with the puffins, the common name rhinoceros puffin has been proposed for the species.
The whiskered auklet is a small seabird of the auk family. It has a more restricted range than other members of its genus, Aethia, living only around the Aleutian Islands and on some islands off Siberia, and breeding on these islands. It is one of the smallest alcids, only the closely related least auklet being smaller. Its name is derived from the long white feathers on its face that are part of its breeding plumage.
Aethia is a genus of four small (85–300g) auklets endemic to the North Pacific Ocean, Bering Sea and Sea of Okhotsk and among some of North America's most abundant seabirds. The relationships between the four true auklets remains unclear. Auklets are threatened by invasive species such as Norway rats because of their high degree of coloniality and crevice-nesting.
Mate choice is one of the primary mechanisms under which evolution can occur. It is characterized by a "selective response by animals to particular stimuli" which can be observed as behavior. In other words, before an animal engages with a potential mate, they first evaluate various aspects of that mate which are indicative of quality—such as the resources or phenotypes they have—and evaluate whether or not those particular trait(s) are somehow beneficial to them. The evaluation will then incur a response of some sort.
Peale's falcon is a subspecies of the peregrine falcon. This subspecies was first identified by the ornithologist Robert Ridgway in 1873, named in honor of Titian Ramsay Peale. These birds are the largest subspecies of peregrines anywhere in the world.
The long-tailed widowbird is a species of bird in the family Ploceidae. The species are found in Angola, Botswana, the Democratic Republic of the Congo, Kenya, Lesotho, South Africa, Eswatini, and Zambia. The long-tailed widowbird is a medium-sized bird and one of the most common in the territories it inhabits. Adult breeding males are almost entirely black with orange and white shoulders (epaulets), long, wide tails, and a bluish white bill. Females are rather inconspicuous, their feathers streaked tawny and black with pale patches on the chest, breast and back, narrow tail feathers, and horn-colored bills.
A courtship display is a set of display behaviors in which an animal, usually a male, attempts to attract a mate; the mate exercises choice, so sexual selection acts on the display. These behaviors often include ritualized movement ("dances"), vocalizations, mechanical sound production, or displays of beauty, strength, or agonistic ability.
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.
A biological ornament is a characteristic of an animal that appears to serve a decorative function rather than a utilitarian function. Many are secondary sexual characteristics, and others appear on young birds during the period when they are dependent on being fed by their parents. Ornaments are used in displays to attract mates, which may lead to the evolutionary process known as sexual selection. An animal may shake, lengthen, or spread out its ornament in order to get the attention of the opposite sex, which will in turn choose the most attractive one with which to mate. Ornaments are most often observed in males, and choosing an extravagantly ornamented male benefits females as the genes that produce the ornament will be passed on to her offspring, increasing their own reproductive fitness. As Ronald Fisher noted, the male offspring will inherit the ornament while the female offspring will inherit the preference for said ornament, which can lead to a positive feedback loop known as a Fisherian runaway. These structures serve as cues to animal sexual behaviour, that is, they are sensory signals that affect mating responses. Therefore, ornamental traits are often selected by mate choice.
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.