Grouse

Grouse /ɡraʊs/ are a group of birds from the order Galliformes, in the family Phasianidae. Grouse are frequently assigned to the subfamily Tetraoninae (sometimes Tetraonidae), a classification supported by mitochondrial DNA sequence studies,[1] and applied by the American Ornithologists' Union,[2] ITIS,[3] and others.[4] Grouse inhabit temperate and subarctic regions of the Northern Hemisphere, from pine forests to moorland and mountainside,[5] from 83°N (rock ptarmigan in northern Greenland) to 28°N (Attwater's prairie chicken in Texas).[6]

For other uses, see Grouse (disambiguation).

Grouse
Temporal range: Early Pliocene to recent
Male sage grouse
Centrocercus urophasianus
Scientific classification
Kingdom: Animalia
Phylum: Chordata
Class: Aves
Order: Galliformes
Family: Phasianidae
Subfamily: Tetraoninae
Vigors, 1825
Genera

Bonasa
Falcipennis
Centrocercus
Dendragapus
Lagopus
Tetrao
Lyrurus
Tetrastes
Tympanuchus
and see text

Synonyms

Tetraonidae Vigors, 1825

Description

Grouse are heavily built like other Galliformes, such as chickens. They range in length from 31 to 95 cm (12 to 37 in), and in weight from 0.3 to 6.5 kg (0.66 to 14.33 lb). Males are larger than females—twice as heavy in the western capercaillie, the largest member of the family. Grouse have feathered nostrils. Their legs covered in feathers down to the toes, and in winter the toes, too, have feathers or small scales on the sides, an adaptation for walking on snow and burrowing into it for shelter. Unlike other Galliformes, they have no spurs.[6]

Feeding and habits

These birds feed mainly on vegetation—buds, catkins, leaves, and twigs—which typically accounts for over 95% of adults' food by weight. Thus, their diets vary greatly with the seasons. Hatchlings eat mostly insects and other invertebrates, gradually reducing their proportion of animal food to adult levels. Several of the forest-living species are notable for eating large quantities of conifer needles, which most other vertebrates refuse. To digest vegetable food, grouse have big crops and gizzards, eat grit to break up food, and have long intestines with well-developed caeca in which symbiotic bacteria digest cellulose.[6]

Forest species flock only in autumn and winter, though individuals tolerate each other when they meet. Prairie species are more social, and tundra species (ptarmigans, Lagopus) are the most social, forming flocks of up to 100 in winter. All grouse spend most of their time on the ground, though when alarmed, they may take off in a flurry and go into a long glide.[6]

Most species stay within their breeding range all year, but make short seasonal movements; many individuals of the ptarmigan (called rock ptarmigan in the US) and willow grouse (called willow ptarmigan in the US) migrate hundreds of kilometers.[6]

Reproduction

In all but one species (the willow ptarmigan), males are polygamous. Many species have elaborate courtship displays on the ground at dawn and dusk, which in some are given in leks. The displays feature males' brightly colored combs and in some species, brightly colored inflatable sacs on the sides of their necks. The males display their plumage, give vocalizations that vary widely between species, and may engage in other activities, such as drumming or fluttering their wings, rattling their tails, and making display flights. Occasionally, males fight.[6]

The nest is a shallow depression or scrape on the ground—often in cover—with a scanty lining of plant material. The female lays one clutch, but may replace it if the eggs are lost. She begins to lay about a week after mating and lays one egg every day or two; the clutch comprises five to 12 eggs. The eggs have the shape of hen's eggs and are pale yellow, sparsely spotted with brown. On laying the second-last or last egg, the female starts 21 to 28 days of incubation. Chicks hatch in dense, yellow-brown down and leave the nest immediately. They soon develop feathers and can fly shortly before they are two weeks old. The female (and the male in the willow grouse) stays with them and protects them until their first autumn, when they reach their mature weights (except in the male capercaillies). They are sexually mature the following spring, but often do not mate until later years.[6]

Populations
A ruffed grouse in Canada

Grouse make up a considerable part of the vertebrate biomass in the Arctic and Subarctic. Their numbers may fall sharply in years of bad weather or high predator populations—significant grouse populations are a major food source for lynx, foxes, martens, and birds of prey. However, because of their large clutches, they can recover quickly.

The three tundra species have maintained their former numbers. The prairie and forest species have declined greatly because of habitat loss, though popular game birds such as the red grouse and the ruffed grouse have benefited from habitat management. Most grouse species are listed by the IUCN as "least concern" or "near threatened", but the greater and lesser prairie chicken are listed as "vulnerable" and the Gunnison grouse is listed as "endangered". Some subspecies, such as Attwater's prairie chicken and the Cantabrian capercaillie, and some national and regional populations are also in danger.[6]

Sexual size dimorphism

Male size selection

The phenotypic difference between males and females is called sexual dimorphism.[7] Male grouse tend to be larger than female grouse,[7] which seems to hold true across all the species of grouse, with some difference within each species in terms of how drastic the size difference is.[7] The hypothesis with the most supporting evidence for the evolution of sexual dimorphism in grouse is sexual selection.[7] Sexual selection favors large males; stronger selection for larger size in males leads to greater size dimorphism.[7] Female size will increase correspondingly as male size increases, and this is due to heredity (but not to the extent of the male size).[7] This is because females that are smaller will still be able to reproduce without a substantial disadvantage, but this is not the case with males.[7] The largest among the male grouse (commonly dubbed 'Biggrouse') attract the greatest numbers of females during their mating seasons,

Mating behavior selection
Main article: Lek mating

Male grouse display lekking behavior, which is when many males come together in one area and put on displays to attract females.[8] Females selectively choose among the males present for traits they find more appealing.[8] Male grouse exhibit two types: typical lekking and exploded lekking.[7] In typical lekking, males display in small areas, and in exploded lekking, displays are done in areas that do not have many resources for females.[7] Male grouse can also compete with one another for access to female grouse through territoriality, in which a male defends a territory which has resources that females need, like food and nest sites.[7] These differences in male behavior in mating systems account for the evolution of body size in grouse.[7] Males of territorial species were smaller than those of exploded lekking species, and males of typical lekking species were the largest overall.[7] The male birds that exhibit lekking behavior, and have to compete with other males for females to choose them, have higher sexual size dimorphism.[9] This supports the hypothesis of sexual selection affecting male body size and also gives an explanation for why some species of grouse have a more drastic difference between male and female body size than others.

Contrast with other bird species

Sexual size dimorphism can manifest itself differently between grouse and other birds. In some cases, the female is dominant over the male in breeding behavior, which can result in females that are larger than the males.[10]

In culture

Grouse are game, and hunters kill millions each year for food, sport, and other uses. In the United Kingdom, this takes the form of driven grouse shooting. The male black grouse's tail feathers are a traditional ornament for hats in areas such as Scotland and the Alps. Folk dances from the Alps to the North American prairies imitate the displays of lekking males.[6]

Species
ImageGenusExtant Species
Falcipennis – spruce grouse
Dendragapus – blue grouse
Lagopus – ptarmigans
Tetrao – capercaillies
Lyrurus – black grouse
Tetrastes – hazel grouse
Bonasa – ruffed grouse
Centrocercus – sage grouse
Tympanuchus – prairie grouse
gollark: I mean, yours is basically tit for tat, yes?
gollark: That way you lose 0 points (except in the initial signalling sequence?) but *other* people will also lose lots.
gollark: THEY need to cooperate.
gollark: You need to be able to detect them and defect against them utterly.
gollark: No, I think it could work if used wisely.

References

Footnotes
  1. Gutiérrez, R. J.; Barrowclough, G. F.; Groth, J. G. (2000). "A classification of the grouse (Aves: Tetroninae) based on mitochondrial DNA sequences" (PDF). Wildlife Biology. 6 (4): 205–212. doi:10.2981/wlb.2000.017. Archived from the original (PDF) on 2015-03-27.
  2. "AOU Checklist of North and Middle American Birds". American Ornithologists' Union. Retrieved 2014-03-13.
  3. "Tetraoninae". Integrated Taxonomic Information System. Retrieved 2013-03-13.
  4. Boyd, John. "Phasianidae: Turkeys, Grouse, Pheasants, Partridges". Aves – A taxonomy in flux. Retrieved 2014-03-13.
  5. Rands, Michael R.W. (1991). Forshaw, Joseph (ed.). Encyclopaedia of Animals: Birds. London: Merehurst Press. p. 91. ISBN 978-1-85391-186-6.
  6. Storch, Ilse; Bendell, J. F. (2003). "Grouse". In Perrins, Christopher (ed.). The Firefly Encyclopedia of Birds. Firefly Books. pp. 184–187. ISBN 978-1-55297-777-4.
  7. Drovetski, S. V.; Rohwer, S.; Mode, N. A. (2006). "Role of sexual and natural selection in evolution of body size and shape: a phylogenetic study of morphological radiation in grouse". Journal of Evolutionary Biology. 19 (4): 1083–1091. doi:10.1111/j.1420-9101.2006.01097.x. PMID 16780509.
  8. Fiske, Peder; Rintamaki, Pekka; Karvonen, Eevi (1998). "Mating success in lekking males: a meta-analysis". Behavioral Ecology. 9 (4): 328–338. doi:10.1093/beheco/9.4.328.
  9. Soulsbury, Carl D; Kervinen, Matti; Lebigre, Christophe (2014). "Sexual size dimorphism and the strength of sexual selection in mammals and birds". Evolutionary Ecology Research. 16: 63–76.
  10. Mueller, H. C. "The Evolution of Reversed Sexual Dimorphism in Owls: An Empirical Analysis of Possible Selective Factors". The Wilson Bulletin. 98 (3): 387–406.

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