Gamebird

Galliformes is an order of heavy-bodied ground-feeding birds that includes turkeys, chickens, quail, and other landfowl. Gallinaceous birds, as they are called, are important in their ecosystems as seed dispersers and predators, and are often reared by humans for their meat and eggs, or hunted as game birds.

The order contains about 290 species, inhabiting every continent except Antarctica, and divided into five families: Phasianidae (including chicken, quail, partridges, pheasants, turkeys, peafowl (peacocks) and grouse), Odontophoridae (New World quail), Numididae (guinea fowl), Cracidae (including chachalacas and curassows), and Megapodiidae (incubator birds like malleefowl and brush-turkeys). They adapt to most environments except for innermost deserts and perpetual ice.

Many gallinaceous species are skilled runners and escape predators by running rather than flying. Males of most species are more colorful than the females, with often elaborate courtship behaviors that include strutting, fluffing of tail or head feathers, and vocal sounds. They are mainly nonmigratory. Several species have been domesticated during their long and extensive relationships with humans.

The name ''galliformes'' derives from " gallus", Latin for "rooster". Common names are gamefowl or gamebirds, landfowl, gallinaceous birds, or galliforms. Galliforms and waterfowl (order Anseriformes) are collectively called ''fowl''.

Systematics and evolution

The living Galliformes were once divided into seven or more families. Despite their distinctive appearance, grouse and turkeys probably do not warrant separation as families due to their recent origin from partridge- or pheasant-like birds. The turkeys became larger after their ancestors colonized temperate and subtropical North America, where pheasant-sized competitors were absent. The ancestors of grouse, though, adapted to harsh climates and could thereby colonize subarctic regions. Consequently, the Phasianidae are expanded in current taxonomy to include the former Tetraonidae and Meleagrididae as subfamilies.

The Anseriformes ( waterfowl) and the Galliformes together make up the Galloanserae. They are basal among the living neognathous birds, and normally follow the Paleognathae (ratites and tinamous) in modern bird classification systems. This was first proposed in the Sibley-Ahlquist taxonomy and has been the one major change of that proposed scheme that was almost universally adopted. However, the Galliformes as they were traditionally delimited are called Gallomorphae in the Sibley-Ahlquist taxonomy, which splits the Cracidae and Megapodiidae as an order "Craciformes". This is not a natural group, however, but rather an erroneous result of the now-obsolete phenetic methodology employed in the Sibley-Ahlquist taxonomy. Phenetic studies do not distinguish between plesiomorphic and apomorphic characters, which leads to basal lineages appearing as monophyletic groups.

Historically, the buttonquails (Turnicidae), mesites (Mesitornithidae) and the hoatzin (''Opisthocomus hoazin'') were placed in the Galliformes, too. The former are now known to be shorebirds adapted to an inland lifestyle, whereas the mesites are probably closely related to pigeons and doves. The relationships of the hoatzin are entirely obscure, and it is usually treated as a monotypic order Opisthocomiformes to signify this.

The fossil record for the Galliformes is incomplete.

Evolution

Galloanserae-like birds were one of the main survivors of the K-T Event, that killed off the rest of the dinosaurs. The dominant birds of the dinosaur era were the enantiornithes, toothed birds that dominated the trees and skies. Unlike those enantiornithes, the ancestors of the galliformes were a niche group that were toothless and ground-dwelling. When the asteroid impact killed off all non-avian dinosaurs, and the dominant birds, it destroyed all creatures that lived in trees and on open ground. The enantiornithes were wiped out, but the ancestors of galliformes were small and lived in the ground (unlike water for Anseriformes) which protected them from the blast and destruction.

Fossils of these galliform-like birds originate in the Late Cretaceous, most notably those of '' Austinornis lentus''. Its partial left tarsometatarsus was found in the Austin Chalk near Fort McKinney, Texas, dating to about 85 million years ago (Mya). This bird was quite certainly closely related to Galliformes, but whether it was a part of these or belongs elsewhere in the little-known galliform branch of Galloanserae is not clear. However, in 2004, Clarke classified it as a member of the larger group Pangalliformes, more closely related to chickens than to ducks, but not a member of the crown group that includes all modern galliformes. Another specimen, PVPH 237, from the Late Cretaceous Portezuelo Formation (Turonian- Coniacian, about 90 Mya) in the Sierra de Portezuelo (Argentina) has also been suggested to be an early galliform relative. This is a partial coracoid of a neornithine bird, which in its general shape and particularly the wide and deep attachment for the muscle joining the coracoid and the humerus bone resembles the more basal lineages of galliforms.

Additional galliform-like pangalliformes are represented by extinct families from the Paleogene, namely the Gallinuloididae, Paraortygidae and Quercymegapodiidae. In the early Cenozoic, some additional birds may or may not be early Galliformes, though even if they are, they are unlikely to belong to extant families:
* †'' Argillipes'' (London Clay Early Eocene of England)
* †'' Coturnipes'' (Early Eocene of England, and Virginia, USA?)
* †'' Palaeophasianus'' (Willwood Early Eocene of Bighorn County, USA)
* †'' Percolinus'' (London Clay Early Eocene of England)
* †'' Amitabha'' (Bridger middle Eocene of Forbidden City, USA) – phasianid?
* †''"Palaeorallus" alienus'' (middle Oligocene of Tatal-Gol, Mongolia)
* †'' Anisolornis'' (Santa Cruz Middle Miocene of Karaihen, Argentina)

From the mid-Eocene onwards – about 45 Mya or so, true galliforms are known, and these completely replace their older relatives in the early Neogene. Since the earliest representatives of living galliform families apparently belong to the Phasianidae – the youngest family of galliforms, the other families of Galliformes must be at least of Early Eocene origin but might even be as old as the Late Cretaceous. The ichnotaxon ''Tristraguloolithus cracioides'' is based on fossil eggshell fragments from the Late Cretaceous Oldman Formation of southern Alberta, Canada, which are similar to chachalaca eggs, but in the absence of bone material, their relationships cannot be determined except that they are apparently avian in origin.

Modern genera of phasianids start appearing around the Oligocene-Miocene boundary, roughly 25–20 Mya. It is not well known whether the living genera of the other, older, galliform families originated around the same time or earlier, though at least in the New World quail, pre-Neogene forms seem to belong to genera that became entirely extinct later on.

A number of Paleogene to mid-Neogene fossils are quite certainly Galliformes, but their exact relationships in the order cannot be determined:

* †Galliformes gen. et sp. indet. (Oligocene) – formerly in ''Gallinuloides''; phasianid?
* †'' Palaealectoris'' (Agate Fossil Beds Early Miocene of Sioux County, USA) – tetraonine?

List of major taxa

For a long time, the pheasants, partridges, and relatives were indiscriminately lumped in the Phasianidae, variously including or excluding turkeys, grouse, New World quail, and guineafowl, and divided into two subfamilies – the Phasianinae (pheasant-like forms) and the Perdicinae (partridge-like forms). This crude arrangement was long considered to be in serious need of revision, but even with modern DNA sequence analyses and cladistic methods, the phylogeny of the Phasianidae has resisted complete resolution.Kimball ''et al.'' (1999, 2001), Crowe ''et al.'' (2006a,b)

A tentative list of the higher-level galliform taxa, listed in evolutionary sequence, is:
* †'' Archaeophasianus'' Lambrecht 1933 (Oligocene? – Late Miocene)
* †'' Argillipes'' Harrison & Walker 1977
* †'' Austinornis'' Clarke 2004 'Pedioecetes'' Baird 1858">Pedioecetes.html" ;"title="'Pedioecetes">'Pedioecetes'' Baird 1858(Austin Chalk Late Cretaceous of Fort McKinney, USA)
* †''Chambiortyx'' Mourer-Chauviré et al. 2013
* †'' Coturnipes'' Harrison & Walker 1977
* †'' Cyrtonyx tedfordi'' (Barstow Late Miocene of Barstow, USA)
* †'' Linquornis'' Yeh 1980 (middle Miocene)
* †'' Namaortyx'' Mourer-Chauviré, Pickford & 2011
* †'' Palaeorallus alienus'' Kuročkin 1968 nomen dubium
* †'' Sobniogallus'' Tomek et al. 2014
* †'' Tristraguloolithus'' Zelenitsky, Hills & Curri 1996 otaxa- cracid?* †'' Procrax'' Tordoff & Macdonald 1957 (middle Eocene? – Early Oligocene)
* †'' Paleophasianus'' Wetmore 1940
* †'' Taoperdix'' Milne-Edwards 1869 (Late Oligocene)
* Family † Gastornithidae? Fürbringer, 1888
** '' Gastornis'' Hébert, 1855 (vide Prévost, 1855) iatryma Cope, 1876(Paleocene-Eocene)
*Family † Sylviornithidae? Mourer-Chauviré & Balouet, 2005
**†'' Sylviornis'' Poplin, 1980 (Holocene)
**†'' Megavitiornis'' Worthy, 2000 (Holocene)

* Family † Paraortygidae Mourer-Chauviré 1992
** †'' Pirortyx'' Brodkorb 1964
** †'' Scopelortyx'' Mourer-Chauviré, Pickford & Senut 2015
** †'' Paraortyx'' Gaillard 1908 sensu Brodkorb 1964
** †'' Xorazmortyx'' Zelenkov & Panteleyev 2019
* Family † Quercymegapodiidae Mourer-Chauviré 1992
** †'' Taubacrex'' Alvarenga 1988
** †'' Ameripodius'' Alvarenga 1995
** †'' Quercymegapodius'' Mourer-Chauviré 1992
* Family Megapodiidae – mound-builders and scrubfowl, or megapodes
** †'' Mwalau'' Worthy et al. 2015 (Lini's megapode)
** †'' Ngawupodius'' & Ivison 1999
** '' Brushturkey group''
*** '' Talegalla'' Lesson 1828
*** '' Leipoa'' Gould 1840 'Progura'' de Vis 1889; ''Chosornis">Progura.html" ;"title="'Progura">'Progura'' de Vis 1889; ''Chosornis'' de Vis 1889; ''Palaeopelargus'' de Vis 1892] (Malleefowl)
*** ''Alectura'' Gray 1831 [''Catheturus'' Swainson 1837] (Australian Brushturkeys)
*** ''Aepypodius'' Oustalet 1880
** '' Scrubfowl group''
*** '' Macrocephalon'' Müller 1846 'Megacephalon'' Gray 1846; ''Megacephalon">Megacephalon.html" ;"title="'Megacephalon">'Megacephalon'' Gray 1846; ''Megacephalon'' Gray 1844 nomen nudum; ''Galeocephala'' Mathews 1926] (Maleos)
*** ''Eulipoa'' Ogilvie-Grant 1893 (Moluccan Megapodes)
*** ''Megapodius'' Gaimard 1823 non (sic) Mathews 1913 [''Megathelia'' Mathews 1914; '' Amelous'' Gloger 1841]
* Family Cracidae – chachalacas, guans and curassows
** †'' Archaealectrornis'' Crowe & Short 1992 (Oligocene)
** †'' Boreortalis'' Brodkorb 1954
** †'' Palaeonossax'' Wetmore 1956 (Brule Late Oligocene of South Dakota, USA)
** Penelopinae Bonaparte 1851 (Guans)
*** '' Chamaepetes'' Wagler 1832 (black & sickle-winged guan)
*** ''Penelopina'' Reichenbach 1861 (Highland Guans)
*** '' Aburria'' Reichenbach 1853 'Opetioptila'' Sundevall 1873; ''Pipile">Opetioptila.html" ;"title="'Opetioptila">'Opetioptila'' Sundevall 1873; ''Pipile'' Bonaparte 1856 non ''Pipilo'' Vieillot 1816; ''Cumana'' Coues 1900]
*** ''Penelope (genus), Penelope'' Merrem 1786 [''Penelopsis'' Bonaparte 1856]
** Cracinae Rafinesque 1815
*** '' Ortalis'' Merrem 1786 'Ganix'' Rafinesque 1815">Ganix.html" ;"title="'Ganix">'Ganix'' Rafinesque 1815 (Chachalacas)
*** ''Oreophasis'' Gray 1844 (Horned Guans)
*** Cracini Rafinesque 1815 (Curassows)
**** ''Nothocrax'' Burmeister 1856 (Nocturnal Curassows)
**** ''Pauxi'' Temminck 1813 'Ourax'' Cuvier 1817; ''Lophocerus">Ourax.html" ;"title="'Ourax">'Ourax'' Cuvier 1817; ''Lophocerus'' Swainson 1837 non Hemprich & Ehrenberg 1833; ''Urax'' Reichenbach 1850]
**** ''Mitu (bird), Mitu'' Lesson 1831 (razor-billed curassows)
**** ''Crax'' Linnaeus 1758
* Suborder Phasiani
** Family † Gallinuloididae – tentatively placed here
*** †'' Gallinuloides'' Eastman 1900 'Palaeobonasa'' Shufeldt 1915">Palaeobonasa.html" ;"title="'Palaeobonasa">'Palaeobonasa'' Shufeldt 1915*** †''Paraortygoides'' Mayr 2000
** Family Numididae – guineafowl
*** ''Guttera'' Wagler 1832
*** '' Numida'' Linnaeus 1764 'Querelea'' Reichenbach 1852">Querelea.html" ;"title="'Querelea">'Querelea'' Reichenbach 1852(Helmeted Guineafowl)
*** ''Acryllium'' Gray 1840 (Vulturine Guineafowl)
*** ''Agelastes'' Bonaparte 1850
** Family Odontophoridae – New World quail
*** †'' Miortyx'' Miller 1944
*** †'' Nanortyx'' Weigel 1963
*** †'' Neortyx'' Holman 1961
*** Ptilopachinae Bowie, Coehn & Crowe 2013
**** '' Ptilopachus'' Swainson 1837
*** Odontophorinae Gould 1844
**** '' Rhynchortyx'' Ogilvie-Grant 1893 (Tawny-faced Quail)
**** '' Oreortyx'' Baird 1858 'Orortyx'' Coues 1882">Orortyx.html" ;"title="'Orortyx">'Orortyx'' Coues 1882(Mountain Quail)
**** ''Dendrortyx'' Gould 1844 (Wood Partridges)
**** '' Philortyx'' Gould 1846 non Des Murs 1854 (Banded Quail)
**** ''Colinus'' Goldfuss 1820 [''Eupsychortyx'' Gould 1844; '' Gnathodon'' 1842; ''Ortygia'' Boie 1826; '' Philortyx'' Des Murs 1854 non Gould 1846] (Bobwhites)
**** '' Callipepla'' Wagler 1832 'Lophortyx'' Bonaparte 1838">Lophortyx.html" ;"title="'Lophortyx">'Lophortyx'' Bonaparte 1838()
**** ''Cyrtonyx'' Gould 1844 ()
**** ''Dactylortyx'' Ogilvie-Grant 1893 (Singing Quail)
**** ''Odontophorus'' Vieillot 1816 [''Dentophorus'' Boie 1828] (Wood Quail)
** Family Phasianidae – pheasants, partridges and relatives
*** †'' Alectoris” pliocaena'' Tugarinov 1940b
*** †'' Bantamyx'' Kuročkin 1982
*** †'' Centuriavis lioae'' Ksepka ''et al.'', 2022
*** †'' Diangallus'' Hou 1985
*** †'' "Gallus" beremendensis'' Jánossy 1976b
*** †'' "Gallus" europaeus'' Harrison 1978
*** †'' Lophogallus'' Zelenkov & Kuročkin 2010
*** †'' Megalocoturnix'' Sánchez Marco 2009
*** †'' Miophasianus'' Brodkorb 1952 Miophasianus'' Lambrecht 1933 nomen nudum ; ''Miogallus">' Miophasianus'' Lambrecht 1933 nomen nudum ; ''Miogallus'' Lambrecht 1933 ]
*** †''Palaeocryptonyx'' Depéret 1892 [''Chauvireria'' Boev 1997; ''Pliogallus'' Tugarinov 1940b non Gaillard 1939; ''Lambrechtia'' Janossy 1974 ]
*** †'' Palaeortyx'' Milne-Edwards 1869 'Palaeoperdix'' Milne-Edwards 1869">Palaeoperdix.html" ;"title="'Palaeoperdix">'Palaeoperdix'' Milne-Edwards 1869*** †''Plioperdix'' Kretzoi 1955 [''Pliogallus'' Tugarinov 1940 nec Gaillard 1939]
*** †''Rustaviornis'' Burchak-Abramovich & Meladze 1972
*** †''Schaubortyx'' Brodkorb 1964
*** †'' Shandongornis'' Yeh 1997
*** †'' Shanxiornis'' Wang et al. 2006
*** †'' Tologuica'' Zelenkov & Kuročkin 2009
*** Subfamily Rollulinae Bonaparte, 1850
*** Subfamily Phasianinae
****Tribe Lerwini von Boetticher, 1939 – snow partridge
****Tribe Ithaginini Wolters 197 – blood pheasant
****Tribe Lophophorini Gray, 1841 – monals, monal-partridges, and tragopans
****Tribe Pucrasiini Wolters 1976 – koklass pheasant
****Tribe Meleagridini – turkey
****Tribe Tetraonini Leach 1820 – grouse
****Tribe Rhizotherini – long-billed partridges
****Tribe Phasianini Horsfield 1821 – true pheasants and partridges
****
***Subfamily Pavoninae
****Tribe Pavonini Rafinesque 1815 – peafowl, arguses, and ''Tropicoperdix'' partridges
****Tribe Polyprectronini Blyth 1852 – peacock-pheasants, Asian spurfowl, and crimson-headed partridge
****Tribe Gallini Brehm 1831 – junglefowl, bamboo partridges, and true francolins
****Tribe Coturnicini Reichenbach, 1848 - Old World quail, snowcocks, and allies

The relationships of many pheasants and partridges were formerly very badly resolved and much confounded by adaptive radiation (in the former) and convergent evolution (in the latter). Thus, the bulk of the Phasianidae was alternatively treated as a single subfamily Phasianinae. The grouse, turkeys, true pheasants, etc., would then become tribes of this subfamily, similar to how the Coturnicinae are commonly split into a quail and a spurfowl tribe. In 2021, Kimball ''et al''. found the family to comprise three distinct subfamilies, with two containing multiple genera; these results were followed by the International Ornithological Congress.

The partridge of Europe is not closely related to other partridge-like Galliformes, as already indicated by its sexually dimorphic coloration and possession of more than 14 rectrices, traits it shares with the other advanced phasianids. However, among these its relationships are obscure; it is unclear whether it is closer to the turkeys or to certain short-tailed pheasants like '' Ithaginis'', '' Lophophorus'', '' Pucrasia'', and '' Tragopan''. In 2021, Kimball ''et al''. found it to belong to the subfamily Phasianini, alongside the true pheasants.

Phylogeny

Living Galliformes based on the work by John Boyd.John Boyd's websit

Description

As their name suggests they are chicken-like in appearance, with rounded bodies and blunt wings, and range in size from small at 15 cm (6 inches) to large at 120 cm (4 feet). They are mainly terrestrial birds and their wings are short and rounded for short-distance flight. Galliforms are anisodactyly, anisodactyl like passerines, but some of the adult males grow spurs that point backwards.

Gallinaceous birds are arboreal or terrestrial animals; many prefer not to fly, but instead walk and run for locomotion. They live 5–8 years in the wild and up to 30 years in captivity. They can be found worldwide and in a variety of habitats, including forests, deserts, and grasslands. They use visual displays and vocalizations for communication, courtship, fighting, territoriality, and brooding.

They have diverse mating strategies: some are monogamous, while others are polygamous or polygynandrous. Male courtship behavior includes elaborate visual displays of plumage. They breed seasonally in accordance with the climate and lay three to 16 eggs per year in nests built on the ground or in trees.

Gallinaceous birds feed on a variety of plant and animal material, which may include fruits, seeds, leaves, shoots, flowers, tubers, roots, insects, snails, worms, lizards, snakes, small rodents, and eggs.

These birds vary in size from the diminutive king quail (''Coturnix chinensis'') (5 in) long and weighing 28–40 g (1–1.4 oz) to the largest extant galliform species, the North American wild turkey (''Meleagris gallopavo''), which may weigh as much as 14 kg (30.5 lb) and may exceed 120 cm (47 in).

The galliform bird species with the largest wingspan and largest overall length (including a train of over 6 feet) is most likely the green peafowl (''Pavo muticus''). Most galliform genera are plump-bodied with thick necks and moderately long legs, with rounded and rather short wings. Grouse, pheasants, francolins, and partridges are typical in their outwardly corpulent silhouettes.

Adult males of many galliform birds have one to several sharp horny spurs on the back of each leg, which they use for fighting. In several lineages, pronounced sexual dimorphism occurs, and among each galliform clade, the more apomorphic ("advanced") lineages tend to be more sexually dimorphic.

Flightlessness

While most Galliformes are rather reluctant flyers, truly flightless forms are unknown among the extant members of the order. Though they are often mischaracterised as weak-flying, Galliformes are actually highly specialised for their particular flight style, bearing extremely powerful flight muscles, and some species are even migratory. Adult snowcocks are, however, flightless, requiring gravity to launch, although juveniles can still fly relatively well.

Nonetheless, a few birds outside the Galliformes crown-group did produce flightlessness.

The genus '' Sylviornis'', a huge prehistorically extinct species of New Caledonia, was flightless, but as opposed to most other flightless birds like ratites or island rails which become flightless due to arrested development of their flight apparatus and subsequently evolve to larger size, ''Sylviornis'' seems to have become flightless simply due to its bulk, with the wing reduction following consequently, not being the reason for its flightlessness.

The gigantic Australian mihirungs, which may be closer to Galliformes than to Anseriformes as traditionally expected, achieved flightlessness more traditionally, strongly reducing their wings and keel. They were massive herbivorous birds, among the largest avian dinosaurs of all time.

By contrast, the stem-galliform '' Scopelortyx'' appears to have been more aerial than modern fowl, with a flight style more suited for gliding and soaring.

Behaviour and ecology

Most of the galliform birds are more or less resident, but some of the smaller temperate species (such as quail) do migrate over considerable distances. Altitudinal migration is evidently quite common amongst montane species, and a few species of subtropical and subarctic regions must reach their watering and/or foraging areas through sustained flight. Species known to make extensive flights include the ptarmigans, sage-grouse (''Centrocercus''), crested partridge, green peafowl, crested argus, mountain peacock-pheasant (''Polyplectron inopinatum''), koklass pheasant (''Pucrasia macrolopha''), Reeves's pheasant, and (''Syrmaticus reevesii''). Other species — most of the New World quail (also known as the ‘toothed quail’), the enigmatic stone partridge (''Ptilopachus petrosus'') of Africa, guineafowl, and eared pheasants (''Crossoptilon'') — are all notable for their daily excursions on foot which may take them many miles in a given day.

Some Galliformes are adapted to grassland habitat, and these genera are remarkable for their long, thin necks, long legs, and large, wide wings. Fairly unrelated species like the crested fireback (''Lophura ignita''), vulturine guineafowl (''Acryllium vulturinum''), and malleefowl (''Leipoa ocellata'') are outwardly similar in their body types (see also convergent evolution).

Most species that show only limited sexual dimorphism are notable for the great amount of locomotion required to find food throughout the majority of the year. Those species that are highly sedentary but with marked ecological transformations over seasons exhibit marked distinct differences between the sexes in size and/or appearance. Eared-pheasants, guineafowl, toothed quail, and the snow partridge (''Lerwa lerwa'') are examples of limited sexual differences and requirements for traveling over wide terrain to forage.

Winter ecology

Gallinaceous birds are well adapted to regions with cold winters. Their larger size, increased plumage, and lower activity levels help them to withstand the cold and conserve energy. Under such conditions, they are able to change their feeding strategy to that of a ruminant. This allows them to feed on and extract energy and nutrients from coarse, fibrous plant material, such as buds, twigs, and conifer needles. This provides a virtually unlimited source of accessible food and requires little energy to harvest.

Food and feeding

Herbivorous to slightly omnivorous galliforms, forming the majority of the group, are typically stoutly built and have short, thick bills primarily adapted for foraging on the ground for rootlets or the consumption of other plant material such as heather shoots. The young birds will also take insects.

Peafowl, junglefowl and most of the subtropical pheasant genera have very different nutritional requirements from typical Palearctic genera. The Himalayan monal (''Lophophorus impejanus'') has been observed digging in the rotting wood of deadfall in a similar manner to woodpeckers to extract invertebrates, even bracing itself with aid of its squared tail. The cheer pheasant (''Catreus wallichi''), crested argus (''Rheinardia ocellata''), the crested partridge (''Rollulus roulroul'') and the crested guineafowl (''Guttera pucherani'') are similar ecologically to the Himalayan monal in that they too forage in rotting wood for termites, ant and beetle larvae, molluscs, crustaceans and young rodents.

Typical peafowl (''Pavo''), most of the peacock-pheasants (''Polyplectron''), the Bulwer's pheasant (''Lophura bulweri''), the ruffed pheasants ('' Chrysolophus'') and the hill partridges ('' Arborophila'') have narrow, relatively delicate bills, poorly suited for digging. These galliform genera prefer instead to capture live invertebrates in leaf litter, in sand, or shallow pools or along stream banks. These genera are also outwardly similar in that they each have exceptionally long, delicate legs and toes and the tendency to frequent seasonally wet habitats to forage, especially during chick-rearing. The blue peafowl (''Pavo cristatus'') is famed in its native India for its appetite for snakes – even poisonous cobras – which it dispatches with its strong feet and sharp bill. The Lady Amherst's pheasant (''Chrysolophus amherstiae''), green peafowl (''Pavo muticus''), Bulwer's pheasant and the crestless fireback (''Lophura erythrophthalma'') are notable for their aptitude to forage for crustaceans such as crayfish and other aquatic small animals in shallow streams and amongst rushes in much the same manner as some members of the rail family ( Rallidae). Similarly, although wild turkeys (''Meleagris gallopavo'') have a diet primarily of vegetation, they will eat insects, mice, lizards, and amphibians, wading in water to hunt for the latter. Domestic hens (''Gallus domesticus'') share this opportunistic behaviour and will eat insects, mice, worms, and amphibians.

The tragopans ('' Tragopan''), mikado pheasant (''Syrmaticus mikado''), and several species of grouse and ptarmigan are exceptional in their largely vegetarian and arboreal foraging habitats; grouse are especially notable for being able to feed on plants rich in terpenes and quinones—such as sagebrush or conifers—which are often avoided by other herbivores. Many species of moderate altitudes—for example the long-tailed pheasants of the genus '' Syrmaticus''—also find a great deal of their daily nutritional requirements in the tree canopies, especially during the snowy and rainy periods when foraging on the ground is dangerous and less than fruitful for a variety of reasons. Although members of the genus ''Syrmaticus'' are capable of subsisting almost entirely on vegetarian materials for months at a time, this is not true for many of the subtropical genera. For example, the great argus (''Argusianus argus'') and crested argus may do most of their foraging during rainy months in the canopy of the jungle, as well. There they are known to forage on slugs, snails, ants, and amphibians to the exclusion of plant material. How they forage in the forest canopy during the rainy months is unknown.

Reproduction

Most galliforms are very prolific, with clutches regularly exceeding 10 eggs in many species. In contrast to most birds which are – at least for a particular breeding season – monogamous, galliforms are often polygynous or polygamous. Such species can be recognized by their pronounced sexual dimorphism.

Galliform young are very precocious and roam with their mothers – or both parents in monogamous species – mere hours after hatching. The most extreme case are the Megapodiidae, where the adults do not brood, but leave incubation to mounds of rotting vegetation, volcanic ash, or hot sand. The young must dig out of the nest mounds after hatching, but they emerge from the eggs fully feathered, and upon leaving the mound, they are able to fly considerable distances.

Common species

Grouse and ptarmigans - Family Tetraonidae

Grouse, ptarmigans, and prairie chickens are all chicken-like birds with short, curved, strong bills, part of the family Tetraonidae. This group includes 25 species residing mostly in North America. They are mainly ground-dwellers and have short, rounded wings for brief flights. They are well adapted to winter by growing feather "snowshoes" on their feet and roosting beneath the snow. They range in size from the white-tailed ptarmigan to the sage grouse. Their plumage is dense and soft and is most commonly found in shades of red, brown, and gray to camouflage to the ground. They are polygamous and male courtship behavior includes strutting and dancing and aggressive fighting for possession of females. The typical clutch size is between seven and 12 eggs.

Turkeys - Family Meleagrididae

Turkeys are large, long-legged birds that can grow up to in height and weigh up to in the wild. They have a long, broad, rounded tail with 14–19 blunt feathers. They have a naked, wrinkled head and feathered body. The North American wild turkey – ''Meleagris gallopavo'' – has five distinct subspecies (Eastern, Rio Grande, Florida sceola Merriam's, and Gould's). Hybrids also exist where the ranges of these subspecies overlap. All are native only to North America, though transplanted populations exist elsewhere. Their plumage differs slightly by subspecies, but is generally dark to black for males, with buff to cream highlights, and generally drab brown for females. The feathers are quite iridescent and can take on distinct reddish/copper hues in sunlight. Their feathers are well defined with broad, square ends, giving the bird the appearance of being covered in scales. Males have a "beard" of coarse black bristles hanging from the center of their upper breasts and tend to have more vibrantly colored plumage than do females. They breed in the spring and their typical clutch size is between 10 and 12 eggs. The ocellated turkey (''Meleagris ocellata''), a different species of turkey, currently exists only in a portion of the Yucatán peninsula. After the 19th and early 20th centuries, wild turkey populations dropped significantly because of hunting and habitat loss. However, populations now flourish again due to hunting management and transplanting. The ocellated turkey, not commonly hunted, is currently threatened due to ongoing habitat loss in the Yucutan.

Pheasants, quail, and partridges - Family Phasianidae

The family is divided into four groups: 30 species of new world quail, residing between Paraguay and Canada, 11 species of Old World quail in Africa, Australia, and Asia, 94 species of partridges, and 48 species of pheasants. This family includes a wide range of bird sizes from a quail to pheasants up to almost . Pheasants and quail have heavy, round bodies and rounded wings. Though they have short legs, they are very fast runners when escaping predators.

Chachalacas - Family Cracidae

Chachalacas are found in the chaparral ecosystems from southern Texas through Mexico and Costa Rica. They are mainly arboreal and make their nests in trees above the ground. They are large, long-legged birds that can grow up to long. They have long tails and are chicken-like in appearance. Their frail-looking yet sturdy nests are made of sticks and leaves. Their clutch size is three or four eggs. The males make a unique, loud, mating call that give them their name. Chachalacas feed mainly on berries, but also eat insects. They are a popular game bird, as their flesh is good to eat. They are also commonly domesticated as pets.

References

Further reading

* Agnolin, Federico L.; Novas, Fernando E. & Lio, Gabriel (2006): Neornithine bird coracoid from the Upper Cretaceous of Patagonia. ''Ameghiniana'' 43(1): 245–248
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* Crowe, Timothy M.; Bloomer, Paulette; Randi, Ettore; Lucchini, Vittorio; Kimball, Rebecca T.; Braun, Edward L. & Groth, Jeffrey G. (2006a): Supra-generic cladistics of landfowl (Order Galliformes). ''Acta Zoologica Sinica'' 52(Supplement): 358–361
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* Crowe, Timothy M.; Bowie, Rauri C.K.; Bloomer, Paulette; Mandiwana, Tshifhiwa G.; Hedderson, Terry A.J.; Randi, Ettore; Pereira, Sergio L. & Wakeling, Julia (2006b): Phylogenetics, biogeography and classification of, and character evolution in, gamebirds (Aves: Galliformes): effects of character exclusion, data partitioning and missing data. ''Cladistics'' 22(6): 495–532. PDF fulltext
* Dyke, Gareth J; Gulas, Bonnie E. & Crowe, Timothy M. (2003): Suprageneric relationships of galliform birds (Aves, Galliformes): a cladistic analysis of morphological characters. '' Zool. J. Linn. Soc.'' 137(2): 227–244. PDF fulltext
* Kimball, Rebecca T.; Braun, Edward L.; Zwartjes, P.W.; Crowe, Timothy M. & Ligon, J. David (1999): A molecular phylogeny of the pheasants and partridges suggests that these lineages are not monophyletic. '' Mol. Phylogenet. Evol.'' 11(1): 38–54. PDF fulltext

* Kimball, Rebecca T.; Braun, Edward L.; Ligon, J. David; Lucchini, Vittorio & Randi, Ettore (2001): A molecular phylogeny of the peacock-pheasants (Galliformes: ''Polyplectron'' spp.) indicates loss and reduction of ornamental traits and display behaviours. '' Biol. J. Linn. Soc.'' 73(2): 187–198. PDF fulltext
* Kimball, Rebecca T.; Braun, Edward L.; Ligon, J. David; Randi, Ettore & Lucchini, Vittorio (2006): Using molecular phylogenetics to interpret evolutionary changes in morphology and behavior in the Phasianidae. ''Acta Zoologica Sinica'' 52(Supplement): 362–365
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* Smith, Edward J.; Shi, Li & Tu, Zhijian (2005): ''Gallus gallus'' aggrecan gene-based phylogenetic analysis of selected avian taxonomic groups. ''Genetica'' 124(1): 23–32. (HTML abstract)
* Zelenitsky, Darla K.; Hills, L.V. & Currie, Philip J. (1996): Parataxonomic classification of ornithoid eggshell fragments from the Oldman Formation (Judith River Group; Upper Cretaceous), Southern Alberta. ''Canadian Journal of Earth Sciences'' 33(12): 1655–1667.