Phasianus

Last updated

Phasianus
Temporal range: Late Miocene-Recent, 5.4–0  Ma
Pheasant.jpg
Mongolian ringneck-type common pheasant (P. colchicus) cock
Scientific classification OOjs UI icon edit-ltr.svg
Domain: Eukaryota
Kingdom: Animalia
Phylum: Chordata
Class: Aves
Order: Galliformes
Family: Phasianidae
Tribe: Phasianini
Genus: Phasianus
Linnaeus, 1758
Type species
Phasianus colchicus
Species

The "typical" pheasant genus Phasianus in the family Phasianidae consists of two species. The genus name is Latin for pheasant.

Contents

Taxonomy

The genus Phasianus was introduced in 1758 by the Swedish naturalist Carl Linnaeus in the tenth edition of his Systema Naturae . [1] The genus name is Latin for "pheasant". The word is derived from the Ancient Greek φἀσιἀνος, phāsiānos, meaning "(bird) of the Phasis". The birds were found by the Argonauts on the banks of the River Phasis (now the Rioni) in Colchis on the east coast of the Black Sea (now western Georgia). [2] The type species of the genus is the common pheasant (Phasianus colchicus). [3]

Species

The genus contains just two species. [4]

MaleFemaleNameCommon nameDistribution
A beautiful pheasant in full glory searching food along the Rhine river - panoramio.jpg Phasianus colchicus 4 hen (Lukasz Lukasik).jpg Phasianus colchicus common pheasant Asia introduced to Europe, North America
Phasianus versicolor in Japan.JPG Phasianus versicolor female.JPG Phasianus versicolor green pheasant Japan

The common pheasant (P. colchicus) has about 30 recognised subspecies forming five or six distinct groups; one is only found on the island of Taiwan off the southern coast of continental China, and the rest on the Asian mainland, reaching west to the Caucasus. Some subspecies have been introduced to Europe, North America and elsewhere, where they have hybridized and become well established.

The green pheasant (P. versicolor) is a species from Japan that which the fossil record suggest diverged about 2.0–1.8 million years ago from P. colchicus. [5]

Fossil remains of a Phasianus pheasant have been found in Late Miocene rocks in China. Additionally, fossil material belonging to a new species of Phasianus was described in 2020 as P. bulgaricus. The fossils were recovered from Miocene (Turolian) strata in Bulgaria. [6] Thus, like many other phasianid genera, this lineage dates back more than 5,000,000 years.

Sexual selection

Phasianus pheasants are a harem polygynous species that are a highly sexually dimorphic genus, where males are large and elaborately ornamented with brightly coloured plumage, ear tufts, wattles, spurs, and long tails, compared to females that are non-ornamented with a dull cryptic plumage. [7] [8] [9] They have a polygynous mating system that is based upon males defending mating territories during breeding season in the early spring to control access to females with higher quality resources and defence against predation. [7] [10] [11] Females are free to move between different male territories, allowing them to benefit from direct or indirect benefits by choosing high quality mates and areas with better resources for their offspring. [11] Phasianus chicks are precocial so males provide no parental care for their young. [7] [10] [11]

A male's ornaments and weaponry are a symbol of status that allow females and rivals to examine a male's fitness and fighting ability. [7] During breeding season, males court females or challenge other males by enlarging their sexual traits, sloping their body towards their opponent or mate while spreading their tail and plumage, inflating the wattle and raising their ear tufts. [11] Older males usually have more exaggerated ornaments and weaponry than younger males, and are more likely to mate and control larger territories. [12] Submissive or juvenile males will conceal their wattle display from bigger males, reducing their chance of mating but minimizing their risk of injury by avoiding physical conflict with a more dominant male. [11] The general brightness of the plumage may also be used to identify healthy males from unhealthy males. [7] Only in cases where males exhibit similar characteristics, do males attack one another. [13]

To display these traits throughout breeding season entails a physiological cost, leading to an endurance rivalry between males, where only males that can afford to display these breeding rituals will pass on their genes to their offspring. [11] [13] An example of this can be seen in the length of a male's spur and the wattle display that is enlarged during sexual displays; both are considered costly as they are highly dependent on nutrition and testosterone levels. [8] [9] [14] [15] [16] Females generally prefer brighter wattles and longer spurs. [8] The brightness in the wattle comes from storing a carotenoid pigment known as astaxanthin in their diet that is inhibited by an infestation of parasites. [8] Only healthy individuals in good physical condition can afford to fully express bigger and brighter wattles, which may also be associated with disease resistance. [8] [16] Spurs function not only as weapons in combat between males but also as an important cue in female choice as the length of the spur signifies the male's phenotypic condition (age, weight, size) and viability. [10] [14] Studies have found that longer spurs resulted in bigger harem sizes compared to males with shorter spurs. [15]

Females will benefit from choosing males with higher expressed ornaments, as her offspring will also inherit these genes, increasing their survival and chance for reproduction (sexy son hypothesis). [11]

Related Research Articles

<span class="mw-page-title-main">Sexual selection</span> Mode of natural selection involving the choosing of and competition for mates

Sexual selection is a mode of natural selection 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.

<span class="mw-page-title-main">Pheasant</span> Bird in family Phasianidae

Pheasants are birds of several genera within the family Phasianidae in the order Galliformes. Although they can be found all over the world in introduced populations, the pheasant genera's native range is restricted to Eurasia. The classification "pheasant" is paraphyletic, as birds referred to as pheasants are included within both the subfamilies Phasianinae and Pavoninae, and in many cases are more closely related to smaller phasianids, grouse, and turkey than to other pheasants.

<span class="mw-page-title-main">Grouse</span> Tribe of birds

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.

<span class="mw-page-title-main">Peafowl</span> Group of large game birds

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.

<span class="mw-page-title-main">Common pheasant</span> Species of bird

The common pheasant is a bird in the pheasant family (Phasianidae). The genus name comes from Latin phasianus, "pheasant". The species name colchicus is Latin for "of Colchis", a country on the Black Sea where pheasants became known to Europeans. Although Phasianus was previously thought to be closely related to the genus Gallus, the genus of junglefowl and domesticated chickens, recent studies show that they are in different subfamilies, having diverged over 20 million years ago.

<span class="mw-page-title-main">Sexual dimorphism</span> Condition where males and females exhibit different characteristics

Sexual dimorphism is the condition where sexes of the same species exhibit different morphological characteristics, particularly characteristics not directly involved in reproduction. The condition occurs in most dioecious species, which consist of most animals and some plants. Differences may include secondary sex characteristics, size, weight, color, markings, or behavioral or cognitive traits. Male-male reproductive competition has evolved a diverse array of sexually dimorphic traits. Aggressive utility traits such as "battle" teeth and blunt heads reinforced as battering rams are used as weapons in aggressive interactions between rivals. Passive displays such as ornamental feathering or song-calling have also evolved mainly through sexual selection. These differences may be subtle or exaggerated and may be subjected to sexual selection and natural selection. The opposite of dimorphism is monomorphism, when both biological sexes are phenotypically indistinguishable from each other.

<span class="mw-page-title-main">Bowerbird</span> Family of birds

Bowerbirds make up the bird family Ptilonorhynchidae. They are renowned for their unique courtship behaviour, where males build a structure and decorate it with sticks and brightly coloured objects in an attempt to attract a mate.

<span class="mw-page-title-main">Green pheasant</span> Species of bird

The green pheasant, also known as the Japanese green pheasant, is an omnivorous bird native to the Japanese archipelago, to which it is endemic. Some taxonomic authorities consider it a subspecies of the common pheasant, Phasianus colchicus. It is the national bird of Japan.

<span class="mw-page-title-main">Ruff (bird)</span> Species of bird

The ruff is a medium-sized wading bird that breeds in marshes and wet meadows across northern Eurasia. This highly gregarious sandpiper is migratory and sometimes forms huge flocks in its winter grounds, which include southern and western Europe, Africa, southern Asia and Australia.

<span class="mw-page-title-main">Blood pheasant</span> Species of bird

The blood pheasant or blood partridge is a galliforme bird in the pheasant family Phasianidae and the only species in the genus Ithaginis. It is a relatively small, short-tailed pheasant that is widespread in the lower Himalayas ranging across North and East India, Nepal, Bhutan, South China and northern Myanmar. It has been classified as Least Concern on the IUCN Red List since 2009, and the global blood pheasant population is thought to be stable.

<span class="mw-page-title-main">Satyr tragopan</span> Species of bird

The satyr tragopan also known as the crimson horned pheasant, is a pheasant found in the Himalayan reaches of India, Tibet, Nepal and Bhutan. They reside in moist oak and rhododendron forests with dense undergrowth and bamboo clumps. They range from 2400 to 4200 meters in summer and 1800 meters in winter. The male is about 70 cm long.

<span class="mw-page-title-main">Crested auklet</span> Species of bird

The crested auklet 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.

<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.

<span class="mw-page-title-main">Guianan cock-of-the-rock</span> Species of bird

The Guianan cock-of-the-rock is a species of cotinga, a passerine bird from South America. It is about 30 cm (12 in) in length and weighs about 200 to 220 g. It is found in tropical rainforests, near its preferred habitat of rocky outcrops. The female's plumage is brownish/dark smokey grey in colour, and generally less noticeable than the males because of their nesting work in rocky areas. The male's feathers are a bright orange. Both have a heavy body, broad-based bill and wear a remarkable half-moon crest on the head. It is one of two species of the genus Rupicola, the other being the Andean cock-of-the-rock. The Guianan cock-of-the-rock lives across the forested region of northeastern South America. Its diet consists mostly of fruit, but they sometimes feast on small snakes and lizards.

<i>Syrmaticus</i> Genus of birds

The genus Syrmaticus contains the five species of long-tailed pheasants. The males have short spurs and usually red facial wattles, but otherwise differ wildly in appearance. The hens (females) and chicks of all the species have a rather conservative and plesiomorphic drab brown color pattern. 5 species are generally accepted in this genus.

<span class="mw-page-title-main">Mate choice</span> One of the primary mechanisms under which evolution can occur

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.

<span class="mw-page-title-main">Wattle (anatomy)</span> Fleshy growth on the head or neck of a bird

A wattle is a fleshy caruncle hanging from various parts of the head or neck in several groups of birds and mammals. Caruncles in birds include those found on the face, wattles, dewlaps, snoods, and earlobes. Wattles are generally paired structures but may occur as a single structure when it is sometimes known as a dewlap. Wattles are frequently organs of sexual dimorphism. In some birds, caruncles are erectile tissue and may or may not have a feather covering.

<span class="mw-page-title-main">Courtship display</span> Communication to start a relationship with someone or to get sexual contact

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.

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.

<span class="mw-page-title-main">Sexual selection in birds</span>

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.

References

  1. Linnaeus, Carl (1758). Systema Naturae per regna tria naturae, secundum classes, ordines, genera, species, cum characteribus, differentiis, synonymis, locis (in Latin). Vol. 1 (10th ed.). Holmiae (Stockholm): Laurentii Salvii. p. 158.
  2. Jobling, James A. (2010). The Helm Dictionary of Scientific Bird Names. London: Christopher Helm. p. 302. ISBN   978-1-4081-2501-4.
  3. Peters, James Lee, ed. (1934). Check-List of Birds of the World. Vol. 2. Cambridge, Massachusetts: Harvard University Press. p. 121.
  4. Gill, Frank; Donsker, David; Rasmussen, Pamela, eds. (July 2021). "Pheasants, partridges, francolins". IOC World Bird List Version 11.2. International Ornithologists' Union. Retrieved 23 August 2021.
  5. Lixun Zhang, Bei An,Niclas Backstrom, Naifa Liu (2013). "Phylogeography-Based Delimitation of Subspecies Boundaries in the Common Pheasant (Phasianus colchicus)". Biochem Genet.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  6. Boev, Zlatozar (2020-03-18). "First European Neogene record of true pheasants from Gorna Sushitsa (SW Bulgaria)". Historia naturalis bulgarica. 41 (5): 33–39. doi: 10.48027/hnb.41.05001 .
  7. 1 2 3 4 5 Mateos, C.; Carranza, J. (1997). "Signals in intra-sexual competition between ring-necked pheasant males". Animal Behaviour. 53 (3): 471–485. doi:10.1006/anbe.1996.0297. S2CID   53197441.
  8. 1 2 3 4 5 Ohlsson, T.; Smith, H. G.; Raberg, L.; Hasselquist, D. (2002). "Pheasant sexual ornaments reflect nutritional conditions during early growth". Proceedings of the Royal Society B: Biological Sciences. 269 (1486): 21–27. doi:10.1098/rspb.2001.1848. PMC   1690866 . PMID   11788032.
  9. 1 2 Briganti, F.; Papeschi, A.; Mugnai, T.; Dessì-Fulgheri, F. (1999). "Effect of testosterone on male traits and behaviour in juvenile pheasants". Ethology Ecology and Evolution. 11 (2): 171–178. Bibcode:1999EtEcE..11..171B. doi:10.1080/08927014.1999.9522834.
  10. 1 2 3 Goransson, G.; Von Schantz, T.; Groberg, I.; Helgee, A.; Wittzell, H. (1990). "Male characteristics, viability and harem size in the pheasant, Phasianus colchicus". Animal Behaviour. 40 (1): 89–104. doi:10.1016/S0003-3472(05)80668-2. S2CID   53145860.
  11. 1 2 3 4 5 6 7 Mateos, C (1998). "Sexual selection in the ring-necked pheasant: A review". Ethology Ecology and Evolution. 10 (4): 313–332. Bibcode:1998EtEcE..10..313M. doi:10.1080/08927014.1998.9522846.
  12. Grahn, M.; Von Schantz, T. (1994). "Fashion and age in pheasants: Age differences in mate choice". Proceedings: Biological Sciences. 255 (1344): 237–241. doi:10.1098/rspb.1994.0034. S2CID   140563409.
  13. 1 2 Mateos, C.; Carranza, J. (1999). "Effects of male dominance and courtship display on female choice in the ring-necked pheasant". Behavioral Ecology and Sociobiology. 45 (3/4): 235–244. doi:10.1007/s002650050558. S2CID   2494456.
  14. 1 2 von Schantz, T.; Göransson, G.; Andersson, G.; Fröberg, I.; Grahn, M.; Helgée, A.; Wittzell, H. (1989). "Female choice selects for a viability-based male trait in pheasants". Nature. 337 (6203): 166–9. Bibcode:1989Natur.337..166V. doi:10.1038/337166a0. PMID   2911350. S2CID   4372336.
  15. 1 2 Mateos, C.; Carranza, J. (1996). "On the intersexual selection for spurs in the ring-necked pheasant". Behavioral Ecology. 7 (3): 362–369. doi: 10.1093/beheco/7.3.362 .
  16. 1 2 Papeschi, A.; Dessì-Fulgheri, F. (2003). "Multiple ornaments are positively related to male survival in the common pheasant". Animal Behaviour. 65 (1): 143–147. doi:10.1006/anbe.2002.2013. S2CID   53149679.

Commons-logo.svg Media related to Phasianus at Wikimedia Commons