Flightless birds are birds that cannot fly. They have, through evolution, lost the ability to fly. [1] There are over 60 extant species, [2] including the well-known ratites (ostriches, emus, cassowaries, rheas, and kiwis) and penguins. The smallest flightless bird is the Inaccessible Island rail (length 12.5 cm, weight 34.7 g). The largest (both heaviest and tallest) flightless bird, which is also the largest living bird in general, is the common ostrich (2.7 m, 156 kg).
Many domesticated birds, such as the domestic chicken and domestic duck, have lost the ability to fly for extended periods, although their ancestral species, the red junglefowl and mallard, respectively, are capable of extended flight. A few particularly bred birds, such as the Broad Breasted White turkey, have become totally flightless as a result of selective breeding; the birds were bred to grow massive breast meat that weighs too much for the bird's wings to support in flight.
Flightlessness has evolved in many different birds independently, demonstrating repeated convergent evolution. [3] There were families of flightless birds, such as the now-extinct Phorusrhacidae, that evolved to be powerful terrestrial predators. Taking this to a greater extreme, the terror birds (and their relatives the bathornithids), eogruids, geranoidids, gastornithiforms, and dromornithids (all extinct) all evolved similar body shapes – long legs, long necks and big heads – but none of them were closely related. Furthermore, they also share traits of being giant, flightless birds with vestigial wings, long legs, and long necks with some of the ratites, although they are not related. [4] [5]
Divergences and losses of flight within ratite lineage occurred right after the K-Pg extinction event wiped out all non-avian dinosaurs and large vertebrates 66 million years ago. [6] The immediate evacuation of niches following the mass extinction provided opportunities for Palaeognathes to distribute and occupy novel environments. New ecological influences selectively pressured different taxa to converge on flightless modes of existence by altering them morphologically and behaviorally. The successful acquisition and protection of a claimed territory selected for large size and cursoriality in Tertiary ancestors of ratites. [7] Temperate rainforests dried out throughout the Miocene and transformed into semiarid deserts, causing habitats to be widely spread across the growingly disparate landmasses. Cursoriality was an economic means of traveling long distances to acquire food that was usually low-lying vegetation, more easily accessed by walking. [7] Traces of these events are reflected in ratite distribution throughout semiarid grasslands and deserts today. [8]
Gigantism and flightlessness in birds are almost exclusively correlated due to islands lacking mammalian or reptilian predators and competition. [9] However, ratites occupy environments that are mostly occupied by a diverse number of mammals. [10] It is thought that they first originated through allopatric speciation caused by breakup of the supercontinent Gondwana. [11] However, later evidence suggests this hypothesis first proposed by Joel Cracraft in 1974 is incorrect. [12] Rather ratites arrived in their respective locations via a flighted ancestor and lost the ability to fly multiple times within the lineage.
Gigantism is not a requirement for flightlessness. The kiwi do not exhibit gigantism, along with tinamous, even though they coexisted with the moa and rheas that both exhibit gigantism. This could be the result of different ancestral flighted birds arrival or because of competitive exclusion. [11] The first flightless bird to arrive in each environment utilized the large flightless herbivore or omnivore niche, forcing the later arrivals to remain smaller. In environments where flightless birds are not present, it is possible that after the K/T Boundary there were no niches for them to fill. They were pushed out by other herbivorous mammals. [10]
New Zealand had more species of flightless birds (including the kiwi, several species of penguins, the takahē, the weka, the moa, and several other extinct species) than any other such location. One reason is that until the arrival of humans roughly a thousand years ago, there were no large mammalian land predators in New Zealand; the main predators of flightless birds were larger birds. [13]
Ratites belong to the superorder Palaeognathae, which include the volant tinamou, and are believed to have evolved flightlessness independently multiple times within their own group. [4] [6] [7] [10] Some birds evolved flightlessness in response to the absence of predators, for example on oceanic islands. Incongruences between ratite phylogeny and Gondwana geological history indicate the presence of ratites in their current locations is the result of a secondary invasion by flying birds. [14] It remains possible that the most recent common ancestor of ratites was flightless and the tinamou regained the ability to fly. [15] However, it is believed that the loss of flight is an easier transition for birds than the loss and regain of flight, which has never been documented in avian history. [7] Moreover, tinamou nesting within flightless ratites indicates ancestral ratites were volant and multiple losses of flight occurred independently throughout the lineage. This indicates that the distinctive flightless nature of ratites is the result of convergent evolution. [16]
Two key differences between flying and flightless birds are the smaller wing bones of flightless birds [17] and the absent (or greatly reduced) keel on their breastbone, which anchors muscles needed for wing movement. [18]
Adapting to a cursorial lifestyle causes two inverse morphological changes to occur in the skeleto-muscular system: the pectoral apparatus used to power flight is paedorphically reduced while peramorphosis leads to enlargement of the pelvic girdle for running. [11] Repeated selection for cursorial traits across ratites suggests these adaptions comprise a more efficient use of energy in adulthood. [7] The name "ratite" comes from the Latin ratis, raft, a vessel with no keel. Their flat sternum is distinct from the typical sternum of flighted birds because it lacks a keel, like a raft. This structure is the place where flight muscles attach and thus allow for powered flight. [16] However, ratite anatomy presents other primitive characters meant for flight, such as the fusion of wing elements, a cerebellar structure, the presence of a pygostyle for tail feathers, and an alula on the wing. [12] These morphological traits suggest some affinities to volant groups. Palaeognathes were one of the first colonizers of novel niches and were free to increase in abundance until the population was limited by food and territory. A study looking at energy conservation and the evolution of flightlessness hypothesized intraspecific competition selected for a reduced individual energy expenditure, which is achieved by the loss of flight. [19]
Some flightless varieties of island birds are closely related to flying varieties, implying flight is a significant biological cost. [19] Flight is the most costly type of locomotion exemplified in the natural world. The energy expenditure required for flight increases proportionally with body size, which is often why flightlessness coincides with body mass. [8] By reducing large pectoral muscles that require a significant amount of overall metabolic energy, ratites decrease their basal metabolic rate and conserve energy. [19] [20] A study looking at the basal rates of birds found a significant correlation between low basal rate and pectoral muscle mass in kiwis. On the contrary, flightless penguins exhibit an intermediate basal rate. This is likely because penguins have well-developed pectoral muscles for hunting and diving in the water. [19] For ground-feeding birds, a cursorial lifestyle is more economical and allows for easier access to dietary requirements. [7] Flying birds have different wing and feather structures that make flying easier, while flightless birds' wing structures are well adapted to their environment and activities, such as diving in the ocean. [21]
Species with certain characteristics are more likely to evolve flightlessness. For example, species that already have shorter wings are more likely to lose flight ability. [22] Some species will evolve flatter wings so that they move more efficiently underwater at the cost of their flight. [23] Additionally, birds that undergo simultaneous wing molt, in which they replace all of the feathers in their wings at once during the year, are more likely to evolve flight loss. [24]
A number of bird species appear to be in the process of losing their powers of flight to various extents. These include the Zapata rail of Cuba, the Okinawa rail of Japan, and the Laysan duck of Hawaii. All of these birds show adaptations common to flightlessness, and evolved recently from fully flighted ancestors, but have not yet completely given up the ability to fly. They are, however, weak fliers and are incapable of traveling long distances by air. [25]
Although selection pressure for flight was largely absent, the wing structure has not been lost except in the New Zealand moas. [11] Ostriches are the fastest running birds in the world and emus have been documented running 50 km/h. [8] At these high speeds, wings are necessary for balance and serving as a parachute apparatus to help the bird slow down. Wings are hypothesized to have played a role in sexual selection in early ancestral ratites and were thus maintained. This can be seen today in both the rheas and ostriches. These ratites utilize their wings extensively for courtship and displays to other males. [12] Sexual selection also influences the maintenance of large body size, which discourages flight. The large size of ratites leads to greater access to mates and higher reproductive success. Ratites and tinamous are monogamous and mate only a limited number of times per year. [26] High parental involvement denotes the necessity for choosing a reliable mate. In a climatically stable habitat providing year-round food supply, a male's claimed territory signals to females the abundance of resources readily available to her and her offspring. [20] Male size also indicates his protective abilities. Similar to the emperor penguin, male ratites incubate and protect their offspring anywhere between 85 and 92 days while females feed. They can go up to a week without eating and survive only off fat stores. The emu has been documented fasting for as long as 56 days. [8] If no continued pressures warrant the energy expenditure to maintain the structures of flight, selection will tend towards these other traits.
In penguins, wing structure is maintained for use in locomotion underwater. [27] Penguins evolved their wing structure to become more efficient underwater at the cost of their efficiency in the air. [28]
The only known species of flightless bird in which wings completely disappeared was the gigantic, herbivorous moa of New Zealand, hunted to extinction by humans by the 15th century. In moa, the entire pectoral girdle is reduced to a paired scapulocoracoid, which is the size of a finger. [29]
Many flightless birds are extinct; this list shows species that are either still extant or became extinct in the Holocene (no more than 11,000 years ago). Extinct species are indicated with a cross (†). A number of species suspected, but not confirmed to be flightless, are also included here.
Longer-extinct groups of flightless birds include the Cretaceous patagopterygiformes, hesperornithids, the Cenozoic phorusrhacids ("terror birds") and related bathornithids, the unrelated eogruids, geranoidids, gastornithiforms, and dromornithids (mihirungs or "demon ducks"), and the plotopterids.
Kiwi are flightless birds endemic to New Zealand of the order Apterygiformes. The five extant species fall into the family Apterygidae and genus Apteryx. Approximately the size of a domestic chicken, kiwi are the smallest ratites.
The common ostrich, or simply ostrich, is a species of flightless bird native to certain large areas of Africa. It is one of two extant species of ostriches, the only living members of the genus Struthio in the ratite order of birds. The other is the Somali ostrich, which was recognized as a distinct species by BirdLife International in 2014 having been previously considered a distinctive subspecies of ostrich.
Cassowaries are flightless birds of the genus Casuarius in the order Casuariiformes. They are classified as ratites: flightless birds without a keel on their sternum bones. Cassowaries are native to the tropical forests of New Guinea, The Moluccas, and northeastern Australia.
Ratites are a polyphyletic group consisting of all birds within the infraclass Palaeognathae that lack keels and cannot fly. They are mostly large, long-necked, and long-legged, the exception being the kiwi, which is also the only nocturnal extant ratite.
Struthionidae is a family of flightless birds, containing the extant ostriches and their extinct relatives. The two extant species of ostrich are the common ostrich and Somali ostrich, both in the genus Struthio, which also contains several species known from Holocene fossils such as the Asian ostrich. The common ostrich is the more widespread of the two living species, and is the largest living bird species. The extinct genus Pachystruthio from the Late Pliocene-Early Pleistocene of Eurasia is one of the largest birds ever.
Elephant birds are extinct flightless birds belonging to the order Aepyornithiformes that were native to the island of Madagascar. They are thought to have become extinct around 1000 AD, likely as a result of human activity. Elephant birds comprised three species, one in the genus Mullerornis, and two in Aepyornis.Aepyornis maximus is possibly the largest bird to have ever lived, with their eggs being the largest known for any amniote. Elephant birds are palaeognaths, and their closest living relatives are kiwi, suggesting that ratites did not diversify by vicariance during the breakup of Gondwana but instead convergently evolved flightlessness from ancestors that dispersed more recently by flying.
Ostriches are large flightless birds. Two living species are recognised, the common ostrich, native to large areas of sub-Saharan Africa, and the Somali ostrich, native to the Horn of Africa.
The southern cassowary, also known as double-wattled cassowary, Australian cassowary, or two-wattled cassowary, is a large flightless black bird, found in Indonesia, Papua New Guinea, and northeastern Australia. It is one of the three living species of cassowary, alongside the dwarf cassowary and the northern cassowary. It is a ratite and therefore related to the emu, ostrich, rhea and kiwi.
The great spotted kiwi, great grey kiwi or roroa is a species of kiwi endemic to the South Island of New Zealand. The great spotted kiwi, as a member of the ratites, is flightless. It is the largest of the kiwi. The rugged topography and harsh climate of the high altitude alpine part of its habitat render it inhospitable to a number of introduced mammalian predators, which include dogs, ferrets, cats, and stoats. Because of this, populations of this species have been less seriously affected by the predations of these invasive species compared to other kiwi. Nonetheless, there has been a 43% decline in population in the past 45 years, due to these predators and habitat destruction. This has led it to be classified as vulnerable. There are less than 16,000 great spotted kiwis in total, almost all in the more mountainous parts of northwest Nelson, the northwest coast, and the Southern Alps. A minority live on island reserves.
The Casuariiformes is an order of large flightless birds that has four surviving members: the three species of cassowary, and the only remaining species of emu. They are divided into either a single family, Casuariidae, or more typically two, with the emu splitting off into its own family, Dromaiidae.
Palaeognathae is an infraclass of birds, called paleognaths or palaeognaths, within the class Aves of the clade Archosauria. It is one of the two extant infraclasses of birds, the other being Neognathae, both of which form Neornithes. Palaeognathae contains five extant orders consisting of four flightless lineages, termed ratites, and one flying lineage, the Neotropic tinamous. There are 47 species of tinamous, five of kiwis (Apteryx), three of cassowaries (Casuarius), one of emus (Dromaius), two of rheas (Rhea) and two of ostriches (Struthio). Recent research has indicated that paleognaths are monophyletic but the traditional taxonomic split between flightless and flighted forms is incorrect; tinamous are within the ratite radiation, meaning flightlessness arose independently multiple times via parallel evolution.
Porzana is a genus of birds in the crake and rail family, Rallidae. Its scientific name is derived from Venetian terms for small rails. The spotted crake is the type species.
The Chilean tinamou is a type of tinamou commonly found in high elevation shrubland in subtropical regions of central Chile.
The great Oʻahu rail or great Oʻahu crake is a little-known extinct bird species from Oʻahu, Hawaiʻi, attested only by a few subfossil bones. The holotype is a right tarsometatarsus found in a flooded sinkhole on the ʻEwa Plain near Barbers Point, the southwestern tip of Oʻahu.
Proapteryx micromeros is an extinct kiwi known from the 16–19 million-year-old early Miocene sediments of the St Bathans Fauna of Otago, New Zealand.
Notopalaeognathae is a clade that contains the order Rheiformes (rheas), the clade Novaeratitae, and the clade Dinocrypturi. Notopalaeognathae was named by Yuri et al. (2013) and defined in the PhyloCode by Sangster et al. (2022) as "the least inclusive crown clade containing Rhea americana, Tinamus major, and Apteryx australis". The exact relationships of this group, including its recently extinct members, have only recently been uncovered. The two lineages endemic to New Zealand, the kiwis and the extinct moas, are not each other's closest relatives: the moas are most closely related to the Neotropical tinamous, and the kiwis are sister to the extinct elephant birds of Madagascar, with kiwis and elephant birds together sister to the cassowaries and emu of New Guinea and Australia. The South American rheas are either sister to all other notopalaeognaths or sister to Novaeratitae. The sister group to Notopalaeognathae is Struthionidae.
Novaeratitae is a proposed clade that was originally defined to contain the recent common ancestors of the orders Casuariiformes and Apterygiformes (kiwis). This clade was named by Yuri et al. (2013) and phylogenetically defined in the PhyloCode by Sangster et al. (2022) as "the least inclusive crown clade containing Apteryx australis and Casuarius casuarius". Recently it has been determined that the elephant birds of the extinct order Aepyornithiformes were the closest relatives of the kiwis, and therefore are part of this group. The implication is that ratites had lost flight independently in each group, as the elephant birds are the only novaeratites found outside Oceania. This clade has been contested by other studies, which find the relationships between the four main clades of non-ostrich palaeognaths to be an unresolved polytomy, with only slightly more genetic support for Novaeritiae over alternative proposals.