Genera: Aenigmatolimnas - Amaurolimnas - Amaurornis - Anurolimnas - Aramides - Aramidopsis - Atlantisia - Canirallus - Coturnicops - Crecopsis - Crex - Cyanolimnas - Dryolimnas - Eulabeornis - Fulica - Gallicrex - Gallinula - Gallirallus - Gymnocrex - Habroptila - Himantornis - Laterallus - Lewinia - Megacrex - Micropygia - Neocrex - Nesoclopeus - Pardirallus - Porphyrio- Porphyrula - Porzana - Rallina - Rallus - Rougetius - Sarothrura - †Pleistorallus - †Vitirallus
Worthy, T.H. 2004: The fossil rails (Aves: Rallidae) of Fiji with descriptions of a new genus and species. Journal of the Royal Society of New Zealand, 34: 295-314.
The rails, or Rallidae, are a large cosmopolitan family of small to medium-sized birds. The family exhibits considerable diversity and the family also includes the crakes, coots, and gallinules. Many species are associated with wetlands, although the family is found in every terrestrial habitat except dry deserts, polar regions and alpine areas above the snow line.
Members of the Rallidae are found on every continent except Antarctica. There are numerous island species. The most common habitats are marshland or dense forest. Rails are especially fond of dense vegetation.
The most typical family members occupy dense vegetation in damp environments near lakes, swamps, or rivers. Reed beds are a particularly favoured habitat. They are omnivorous, and those that migrate do so at night: most nest in dense vegetation. In general, they are shy and secretive birds, and are difficult to observe.
Most species walk and run vigorously on strong legs, and have long toes which are well adapted to soft, uneven surfaces. They tend to have short, rounded wings and although they are generally weak fliers, they are, nevertheless, capable of covering long distances.
Island species often become flightless, and many of them are now extinct following the introduction of terrestrial predators such as cats, rats and pigs.
Many reedbed species are secretive (apart from loud calls), crepuscular, and have laterally flattened bodies. In the Old World, long-billed species tend to be called rails and short-billed species crakes. North American species are normally called rails irrespective of bill length. The smallest of these is the Swinhoe's Rail, at 13 cm (5 inches) and 25 grams.
The larger species are also sometimes given other names. The black coots are more adapted to open water than their relatives, and some other large species are called gallinules and swamphens. The largest of this group is the Takahē, at 65 cm (26 inches) and 2.7 kg (6 lbs).
The rails have suffered disproportionally from human changes to the environment and it is estimated that several hundred species of island rail have become extinct because of this. Several island species of rail remain endangered and conservation organisations and governments continue to work to prevent their extinction.
The rails are a fairly homogeneous family of small to medium sized ground living birds. They vary in length from 12 cm to 63 cm and in weight from 20 g to 3000 g. Some species have long necks and in many cases they are laterally compressed. The bill is the most variable feature within the family: in some species it is longer than the head (like the Clapper Rail of the Americas), in others it may be short and wide (as in the coots), or massive (as in the purple gallinules). A few coots and gallinules have a "frontal shield", which is a fleshy rearward extension of the upper bill. The most complex frontal shield is found in the Horned Coot.
Rails exhibit very little sexual dimorphism in either plumage or size.
Flight and flightlessness
The wings of all rails are short and rounded. The flight of those Rallidae able to fly, while not very powerful, can be sustained for long periods of time and many species undertake annual migrations. The weakness of their flight, however, means that they are easily blown off course and thus are common vagrants, a characteristic that has led them to colonize many isolated oceanic islands. Furthermore, these birds often prefer to run rather than fly, especially when in dense habitat. Some are also flightless at some time during their moult period.
Many island rails are flightless because small island habitats without threatening predators often eliminate the need to fly or move long distances. Flight makes intense demands, with the keel and flight muscles taking up to a quarter of a bird's weight in Rallidae species. Reducing the flight muscles, along with the corresponding lowering in metabolic demands, reduces the flightless rail's energy expenditures. For this reason flightlessness makes it easier to survive and colonize an island where resources may be limited. Flightlessness can evolve extremely rapidly in island rails; it took as little as 125,000 years for the Laysan Rail to lose the power of flight and evolve the reduced, stubby wings only useful to keep balance when running quickly.
Behavior and ecology
In general, members of Rallidae are omnivorous generalists. Many species will eat invertebrates, as well as fruit or seedlings. A few species are primarily vegetarian.
The calls of Rallidae species vary and are often quite loud. Some are whistle-like or squeak-like, while others are "unbirdlike". Loud calls are useful in dense vegetation or at night where it is difficult to see another member of the species. Some calls are territorial.
The breeding behavior of many Rallidae species are poorly understood or unknown. Most are thought to be monogamous, although polygyny and polyandry have been reported.
Most often, there are five to ten eggs. Clutches as small as one or as large as fifteen eggs are known.
Egg clutches may not always hatch at the same time. Chicks become mobile after a few days. They will often remain dependent on their parents until fledging, which happens at around one month of age.
Rallidae and humans
Some of the larger, more abundant rails are hunted and their eggs collected for food. The Wake Island Rail was hunted to extinction by the starving Japanese garrison after the island was cut off from supply during World War II.
The Guam Rail is an example of an island species that has been badly affected by introduced species.
At least two species - the Common Moorhen and the American Purple Gallinule - have been considered pests.
Threats and conservation
Due to their tendencies towards flightlessness, many island species have been unable to cope with introduced species. The most dramatic human caused extinctions occurred in the Pacific Ocean as people colonised the islands of Melanesia, Polynesia and Micronesia, during which an estimated 750-1800 species of bird went extinct, half of which were rails. Some species which came close to extinction, such as the Lord Howe Woodhen, and the Takahē, have made modest recoveries due to the efforts of conservation organisations. The Guam Rail came perilously close to extinction when Brown tree snakes were introduced to Guam but some of the last remaining individuals were taken into captivity and are breeding well, although attempts to reintroduce it have met with mixed results.
Systematics and evolution
The family Rallidae has traditionally been grouped with two families of larger birds, the cranes and bustards, as well as several smaller families of usually "primitive" mid-sized amphibious birds, to make up the order Gruiformes. The alternative Sibley-Ahlquist taxonomy, which has been widely accepted in America, raises the family to ordinal level as the Ralliformes. Given the uncertainly about gruiform monophyly, this may or may not be correct; it certainly seems more justified than most of the Sibley-Ahlquist proposals. On the other hand, such a group would probably also include the Heliornithidae (finfoots and Sungrebe), an exclusively tropical group that is somewhat convergent with grebes, and usually united with the rails in the Ralli.
Extant (living) genera
Himanthornis - Nkulengu Rail
Sarothrura - flufftails (9 species)
Canirallus (3 species)
Coturnicops (3 species)
Micropygia - Ocellated Crake
Rallina - forest-rails (8 species)
Anurolimnas (3 species)
Atlantisia - Inaccessible Island Rail
Laterallus (10 species)
Nesoclopeus (1 living species, 1 recently extinct)
Gallirallus - Austropacific rails (11-12 living species, 3-5 recently extinct)
Rallus - typical rails (some 9 living species)
Lewinia (3 species; sometimes included in Rallus)
Dryolimnas (1 living species, 1 recently extinct)
Crecopsis - African Crake (sometimes included in Crex)
Crex - Corn Crake
Rougetius - Rouget's Rail
Aramidopsis - Snoring Rail
Aramides - wood-rails (8-9 living species, possibly 1 recently extinct)
Amaurolimnas - Uniform Crake
Gymnocrex (3 species)
Amaurornis - bush-hens (9 species)
Porzana - typical crakes (13 living species, 4-5 recently extinct)
Aenigmatolimnas - Striped Crake
Cyanolimnas - Zapata Rail
Neocrex (2 species)
Pardirallus (3 species)
Eulabeornis - Chestnut Rail
Habroptila - Invisible Rail
Megacrex - New Guinea Flightless Rail
Gallicrex - Watercock
Porphyrio - swamphens and purple gallinules (6 living species, 2-5 recently extinct; includes Notornis and Porphyrula)
Gallinula - typical gallinules (7-9 living species, 1-3 recently extinct; includes Edithornis and Pareudiastes)
Fulica - coots (c.10 living species, 1 recently extinct)
Additionally, there are many prehistoric rails of extant genera, known only from fossil or subfossil remains, such as the Ibiza Rail (Rallus eivissensis). These have not been listed here; see the genus accounts and the articles on fossil and Late Quaternary prehistoric birds for these species.
Pieter van den Broecke's 1617 drawing of the Red Rail of Mauritius, Aphanapteryx bonasia
Recently extinct genera
Genus Nesotrochis - cave-rails (3 species; extinct prehistoric or later)
Genus Diaphorapteryx - Hawkins' Rail (extinct 19th century)
Genus Aphanapteryx (2 species; extinct mid-18th century)
Genus Cabalus - Chatham Rail (sometimes included in Gallirallus; extinct c. 1900)
Genus Mundia - Ascension Flightless Crake - formerly included in Atlantisia; (late 17th century)
Genus Aphanocrex - St Helena Swamphen (formerly included in Atlantisia; extinct 16th century)
The undescribed Fernando de Noronha Rail, genus and species undetermined, probably survived to historic times.
Late Quaternary prehistoric extinctions
Genus Capellirallus - Snipe-rail
Genus Vitirallus - Viti Levu Rail. The holotype of Vitirallus watlingiis in the collection of the Museum of New Zealand Te Papa Tongarewa.
Genus Hovacrex - Hova-gallinule
and see genus accounts
Fossil species of long-extinct prehistoric rails are richly documented from the well-researched formations of Europe and North America, as well from the less comprehensively studied strata elsewhere:
Genus Eocrex (Wasatch Early Eocene of Steamboat Springs, USA)
Genus Palaeorallus (Wasatch Early Eocene of Wyoming, USA)
Genus Parvirallus (Early - Middle Eocene of England)
Genus Aletornis (Bridger Middle Eocene of Uinta County, USA)[verification needed] - includes Protogrus
Genus Fulicaletornis (Bridger Middle Eocene of Henry's Fork, USA)
Genus Latipons (Middle Eocene of Lee-on-Solent, England)
Genus Ibidopsis (Hordwell Late Eocene of Hordwell, UK)
Genus Quercyrallus (Late Eocene -? Late Oligocene of France)
Genus Belgirallus (Early Oligocene of WC Europe)
Genus Rallicrex (Corbula Middle/Late Oligocene of Kolzsvár, Romania)
Rallidae gen. et sp. indet. (Late Oligocene of Billy-Créchy, France)
Genus Palaeoaramides (Late Oligocene/Early Miocene - Late Miocene of France)
Genus Rhenanorallus (Late Oligocene/Early Miocene of Mainz Basin, Germany)
Genus Paraortygometra (Late Oligocene/?Early Miocene -? Middle Miocene of France) - includes Microrallus
Genus Pararallus (Late Oligocene? - Late Miocene of C Europe) - possibly belongs in Palaeoaramides
Rallidae gen. et sp. indet. (Bathans Early/Middle Miocene of Otago, New Zealand)
Rallidae gen. et sp. indet. (Bathans Early/Middle Miocene of Otago, New Zealand)
Genus Miofulica (Anversian Black Sand Middle Miocene of Antwerp, Belgium)
Genus Miorallus (Middle Miocene of Sansan, France -? Late Miocene of Rudabánya, Hungary)
Genus Youngornis (Shanwang Middle Miocene of Linqu, China)
Rallidae gen. et sp. indet. (Sajóvölgyi Middle Miocene of Mátraszõlõs, Hungary)
Rallidae gen. et sp. indet. (Middle Miocene of Grive-Saint-Alban, France)
Rallidae gen. et sp. indet. (Late Miocene of Lemoyne Quarry, USA)
Rallidae gen. et sp. indet. UMMP V55013-55014; UMMP V55012/V45750/V45746 (Rexroad Late Pliocene of Saw Rock Canyon, USA)
Rallidae gen. et sp. indet. UMMP V29080 (Rexroad Late Pliocene of Fox Canyon, USA)
Genus Creccoides (Blanco Late Pliocene/Early Pleistocene of Crosby County, USA)
Rallidae gen. et sp. indet. (Bermuda, West Atlantic)
Rallidae gen. et sp. indet. (formerly Fulica podagrica) (Late Pleistocene of Barbados)
Genus Pleistorallus (mid-Pleistocene New Zealand). The holotype of Pleistorallus flemingiis in the collection of the Museum of New Zealand Te Papa Tongarewa.
Doubtfully placed here
These taxa may or may not have been rails:
Genus Ludiortyx (Late Eocene) - includes "Tringa" hoffmanni, "Palaeortyx" blanchardi, "P." hoffmanni
Genus Telecrex (Irdin Manha Late Eocene of Chimney Butte, China)
Genus Amitabha (Bridger middle Eocene of Forbidden City, USA) - phasianid?
Genus Palaeocrex (Early Oligocene of Trigonias Quarry, USA)
Genus Rupelrallus (Early Oligocene of Germany)
Neornithes incerta sedis (Late Oligocene of Riversleigh, Australia)
Genus Euryonotus (Pleistocene of Argentina)
The presumed scolopacid wader Limosa gypsorum (Montmartre Late Eocene of France) is sometimes considered a rail and then placed in the genus Montirallus.
^ a b Horsfall & Robinson (2003): pp. 206-207
^ a b Horsfall & Robinson (2003): p. 208
^ a b Horsfall & Robinson (2003): p. 210
^ Horsfall & Robinson (2003): p. 209
^ McNab & Ellis (2006)
^ McNab (1994)
^ Slikas et al. (2002)
^ Horsfall & Robinson (2003): p.207
^ a b Horsfall & Robinson (2003): pp. 209-210
^ a b Horsfall & Robinson (2003): p. 211
^ BLI (2007)
^ Steadman (2006)
^ "Vitirallus watlingi; holotype". Collections Online. Museum of New Zealand Te Papa Tongarewa. Retrieved 18 July 2010.
^ Mlíkovský (2002)
^ A small species of rail: Hugueney et al. (2003)
^ Dozens of mostly broken isolated skull and limb bones of a rail or crake the size of a Slaty-breasted or small Buff-banded Rail: Worthy et al. (2007)
^ Quadrate (MNZ S.40957) and 2 femora (MNZ S.42658, S.42785) of a rail or crake the size of a large Buff-banded Rail: Worthy et al. (2007)
^ Several limb bones of a smallish rail: Gál et al. (1998-99)
^ Partial hand of a Common Moorhen-sized rail: Ballmann (1969)
^ Storrs L. Olson: A new species of Nesotrochis from Hispaniola, with notes on other fossil rails from the West Indies (Aves: Rallidae) In: Proceedings of the Biological Society of Washington 87, 38:p 439-450, 1974
^ Worthy, T.H. 1997: A mid-Pleistocene rail from New Zealand. Alcheringa: an Australasian journal of palaeontology, 21: 71-78. doi:10.1080/03115519708619186
^ "Pleistorallus flemingi; holotype". Collections Online. Museum of New Zealand Te Papa Tongarewa. Retrieved 18 July 2010.
^ Specimen QM F40203. A left carpometacarpus piece of a bird about the size of Lewin's Rail. Probably from a rail, but it is too damaged to determine its affiliations more precisely: Boles (2005)
^ Olson (1985), Mlíkovský (2002)
Ballmann, Peter (1969): Les Oiseaux miocènes de la Grive-Saint-Alban (Isère) [The Miocene birds of Grive-Saint-Alban (Isère)]. Geobios 2: 157-204. [French with English abstract] doi:10.1016/S0016-6995(69)80005-7 (HTML abstract)
BirdLife International (BLI) (2007): Wake Island Rail BirdLife Species Factsheet. Retrieved 2007-07-04.
Boles, Walter E. (2005): A New Flightless Gallinule (Aves: Rallidae: Gallinula) from the Oligo-Miocene of Riversleigh, Northwestern Queensland, Australia. (2005) Records of the Australian Museum 57(2): 179–190. ODF fulltext
Gál, Erika; Hír, János; Kessler, Eugén & Kókay, József (1998–99): Középsõ-miocén õsmaradványok, a Mátraszõlõs, Rákóczi-kápolna alatti útbevágásból. I. A Mátraszõlõs 1. lelõhely [Middle Miocene fossils from the sections at the Rákóczi chapel at Mátraszőlős. Locality Mátraszõlõs I.]. Folia Historico Naturalia Musei Matraensis 23: 33-78. [Hungarian with English abstract] PDF fulltext
Horsfall, Joseph A. & Robinson, Robert (2003): Rails. In: Perrins, Christopher (ed.): Firefly Encyclopedia of Birds. Firefly Books.
Hugueney, Marguerite; Berthet, Didier; Bodergat, Anne-Marie; Escuillié, François; Mourer-Chauviré, Cécile & Wattinne, Aurélia (2003): La limite Oligocène-Miocène en Limagne: changements fauniques chez les mammifères, oiseaux et ostracodes des différents niveaux de Billy-Créchy (Allier, France) [The Oligocene-Miocene boundary in Limagne: faunal changes in the mammals, birds and ostracods from the different levels of Billy-Créchy (Allier, France)] [French with English abstract]. Geobios 36(6): 719–731. doi:10.1016/j.geobios.2003.01.002 (HTML abstract)
McNab, B.K. (1994): Energy conservation and the evolution of flightlessness in birds. Am. Nat. 144(4): 628-642. HTML abstract and first page image
McNab, B.K. & Ellis, H.I. (2006): Flightless rails endemic to islands have lower energy expenditures and clutch sizes than flighted rails on islands and continents. Comparative Biochemistry and Physiology A - Molecular & Integrative Physiology 145(3): 295-311. doi:doi:10.1016/j.cbpa.2006.02.025 (HTML fulltext)
Mlíkovský, Jirí (2002): Cenozoic Birds of the World, Part 1: Europe. Ninox Press, Prague. ISBN 80-901105-3-8 PDF fulltext
Olson, Storrs L. (1985): Section X.D.2.b. Scolopacidae. In: Farner, D.S.; King, J.R. & Parkes, Kenneth C. (eds.): Avian Biology 8: 174-175. Academic Press, New York.
Slikas, B.; Olson, Storrs L. & Fleischer, R.C. (2002): Rapid, independent evolution of flightlessness in four species of Pacific Island rails (Rallidae): an analysis based on mitochondrial sequence data. J. Avian Biol. 33(1): 5-14. doi:10.1034/j.1600-048X.2002.330103.x (HTML fulltext)
Steadman, David William (2006): Extinction and Biogeography of Tropical Pacific Birds. University of Chicago Press. ISBN 0226771423.
Worthy, Trevor H.; Tennyson, A.J.D.; Jones, C.; McNamara, J.A. & Douglas, B.J. (2007): Miocene waterfowl and other birds from central Otago, New Zealand. J. Syst. Palaeontol. 5(1): 1-39. doi:10.1017/S1477201906001957 (HTML abstract)