Charadriiformes

Order of birds

Charadriiformes Rango temporal: Cretácico superior - Presente ,75–0  Ma Pre Ꞓ O S D C PAG T J K Pg norte
Varios miembros de la orden
clasificación cientifica
Reino:	Animalia
Filo:	Chordata
Clase:	Aves
Infraclase:	Neognathae
Clade :	Neoaves
Clade :	Aequorlitornithes
Pedido:	Charadriiformes Huxley , 1867
Familias
Ver texto.

Charadriiformes ( / k ə r æ d r i . Ɪ f ɔr m i z / , desde Charadrius , los género tipo de la familia Charadriidae ) es una orden diverso de pequeñas a medianas y grandes aves . Incluye alrededor de 350 especies y tiene miembros en todas partes del mundo. La mayoría de las aves carradriiformes viven cerca del agua y comen invertebrados u otros animales pequeños; sin embargo, algunos son pelágicos (aves marinas), otros frecuentan los desiertos y algunos se encuentran en bosques densos.

Taxonomía, sistemática y evolución

El pedido se dividía anteriormente en tres subórdenes:

• Los limícolas (o "Charadrii"): aves playeras típicas, la mayoría de las cuales se alimentan sondeando en el lodo o recogiendo objetos de la superficie tanto en ambientes costeros como de agua dulce.
• Las gaviotas y sus aliados (o " Lari "): son especies generalmente de mayor tamaño que extraen peces del mar. Varias gaviotas y skúas también tomarán alimentos de las playas o robarán especies más pequeñas, y algunas se han adaptado a los ambientes del interior.
• Los alcas (o "Alcae") son especies costeras que anidan en acantilados y "vuelan" bajo el agua para pescar.

La taxonomía de Sibley-Ahlquist agrupa a todos los Charadriiformes junto con otras aves marinas y rapaces en un orden Ciconiiformes muy ampliado . Sin embargo, la resolución de la técnica de hibridación ADN-ADN utilizada por Sibley & Ahlquist no fue suficiente para resolver adecuadamente las relaciones en este grupo y, de hecho, parece que los Charadriiformes constituyen un linaje único grande y muy distintivo de aves modernas propias. . ^[1]

Los alces, generalmente considerados distintos debido a su peculiar morfología, están más probablemente relacionados con las gaviotas, siendo la "distinción" el resultado de la adaptación para el buceo. Según una investigación reciente, ^[2] una mejor disposición puede ser la siguiente:

Familias en orden taxonómico

Esta es una lista de las familias carradriiformes , presentadas en orden taxonómico .

• Suborden Scolopaci : limícolas con forma de agachadiza
  • Familia Scolopacidae : agachadiza, playeritos, falaropos y aliados
• Suborden Thinocori : charadriformes aberrantes
  • Familia Rostratulidae : agachadiza pintada
  • Familia Jacanidae : jacanas
  • Familia Thinocoridae : seednipe
  • Familia Pedionomidae : vagabundo de las llanuras
• Suborden Lari : gaviotas y aliados
  • Familia Laridae : gaviotas, charranes y skimmers
  • Familia Alcidae : frailecillos, araos, araos y aliados
  • Familia Stercorariidae : skúas
  • Familia Glareolidae : canasteras y corderos
  • Familia Pluvianidae : chorlito egipcio
  • Familia Dromadidae : chorlito cangrejo
• Suborden Turnici : codornices
  • Familia Turnicidae : codornices
• Suborden Chionidi : rodillas gruesas y aliados
  • Familia Burhinidae : rodillas gruesas
  • Familia Chionididae : sheathbills
  • Familia Pluvianellidae : Chorlito de Magallanes
• Suborden Charadrii : limícolas con aspecto de chorlito
  • Familia Ibidorhynchidae : ibisbill
  • Familia Recurvirostridae : avocetas y zancos
  • Familia Haematopodidae : ostreros
  • Familia Charadriidae : chorlitos y avefrías

De manera más conservadora, el Thinocori podría incluirse en el Scolopaci (este suborden combinado se llama Limicoli) y el Chionidi en el Charadrii. Los subórdenes Thincori, Scolopaci, Chionidi y Charadri se conocen comúnmente como limícolas . Algunas fuentes de taxonomía colocan a la familia Glareolidae en su propio suborden, en lugar de clasificarse en el suborden Lari. ^[3] Los codornices son de posición indeterminada o basal en el grupo Lari-Scolopaci sensu lato . El arreglo que se presenta aquí es un consenso de los estudios recientes. ^[4]

Charadriiformes

Charadrii Chionida Burhinidae   Burhinus     Esacus       Chionidae Chionis   Pluvianellidae Pluvianellus       Charadriida Pluvianidae Pluviano       Pluvialidae Pluvialis       Ibidorhynchidae Ibidorhyncha   Haematopodidae Haematopus     Recurvirostridae   Recurvirostra       Cladorhynchus     Himantopus           Charadriidae Charadriinae   Oreopholus         Phegornis     Zonibyx         Eudromias       Afroxyechus       Charadrius     Thinornis               Vanellinae Vanellus   Anarhynchinae   Erythrogonys       Peltohyas       Eupoda       Anarhynchus     Ochthodromus                       Limicoli Jacanida Thincoroidea Pedionomidae Pedionomus   Thinocoridae   Attagis     Thinocorus       Jacanoidea Rostratulidae   Nycticryphes     Rostratula     Jacanidae     Hydrophasianus     Jacana         Actophilornis       Metopidius       Microparra     Irediparra               Scolopacida Scolopacidae Numeniinae   Bartramia     Numenius       Limosinae Limosa     Arenariinae   Limicola     Ereunetes     Calidris       Arenaria     Prosobonia         Tringinae     Xenus     Phalaropus         Actitis     Tringa       Scolopacinae     Lymnocryptes     Limnodromus         Scolopax       Gallinago       Chubbia     Coenocorypha                       Lari Turnicida   Ortyxelos     Turnix     Larida Glareoloidea Dromadidae Dromas ardeola   Glareolidae   Stiltia     Rhinoptilus       Cursorius     Glareola           Alcoidea Stercorariidae Stercorarius   Alcidae Fraterculinae     Cerorhinca     Fratercula         Ptychoramphus     Aethia       Alcinae   Brachyramphus       Cepphus       Synthliboramphus         Uria     Alle         Alca     †Pinguinus                 Laroidea Laridae Gyginae Gygis   Rynchopinae Rynchops   Anoinae   Anous     Procelsterna     Sterninae   Onychoprion       Sternula       Phaetusa         Gelochelidon     Hydroprogne         Larosterna       Chlidonias       Thalasseus     Sterna                 Larinae   Creagrus       Hydrocoloeus     Rhodostethia         Rissa       Pagophila     Xema           Saundersilarus       Chroicocephalus       Leucophaeus       Larus     Ichthyaetus

Cladogram based on Baker, A.J. et al. (2012)^[5] and Boyd, J. H. et al. (2016) ^[3]

Evolution history

That the Charadriiformes are an ancient group is also borne out by the fossil record. Alongside the Anseriformes, the Charadriiformes are the only other order of modern bird to have an established fossil record within the late Cretaceous, alongside the other dinosaurs. Much of the Neornithes' fossil record around the Cretaceous–Paleogene extinction event is made up of bits and pieces of birds which resemble this order. In many, this is probably due to convergent evolution brought about by semiaquatic habits. Specimen VI 9901 (López de Bertodano Formation, Late Cretaceous of Vega Island, Antarctica) is probably a basal charadriiform somewhat reminiscent of a thick-knee.^[6] However, more complete remains of undisputed charadriiforms are known only from the mid-Paleogene onwards. Present-day orders emerged around the Eocene-Oligocene boundary, roughly 35-30 mya. Basal or unresolved charadriiforms are:

• "Morsoravis" (Late Paleocene/Early Eocene of Jutland, Denmark) - a nomen nudum?
• Jiliniornis (Huadian Middle Eocene of Huadian, China) - charadriid?
• Boutersemia (Early Oligocene of Boutersem, Belgium) - glareolid?
• Turnipax (Early Oligocene) - turnicid?
• Elorius (Early Miocene Saint-Gérand-le-Puy, France)
• "Larus" desnoyersii (Early Miocene of SE France) - larid? stercorarid?
• "Larus" pristinus (John Day Early Miocene of Willow Creek, USA) - larid?
• Charadriiformes gen. et sp. indet. (Bathans Early/Middle Miocene of Otago, New Zealand) - charadriid? scolopacid?^[7]
• Charadriiformes gen. et sp. indet. (Bathans Early/Middle Miocene of Otago, New Zealand) - charadriid? scolopacid?^[8]
• Charadriiformes gen. et sp. indet. (Bathans Early/Middle Miocene of Otago, New Zealand) - larid?^[9]
• Charadriiformes gen. et sp. indet. (Sajóvölgyi Middle Miocene of Mátraszõlõs, Hungary^[10]
• "Totanus" teruelensis (Late Miocene of Los Mansuetos, Spain) - scolopacid? larid?

The "transitional shorebirds" ("Graculavidae") are a generally Mesozoic form taxon formerly believed to constitute the common ancestors of charadriiforms, waterfowl and flamingos. They are now assumed to be mostly basal taxa of the charadriiforms and/or "higher waterbirds", which probably were two distinct lineages 65 mya already,^{[citation needed]} and few if any are still believed to be related to the well-distinct waterfowl. Taxa formerly considered graculavids are:

• Laornithidae - charadriiform? gruiform?
  • Laornis (Late Cretaceous?)
• "Graculavidae"
  • Graculavus (Lance Creek Late Cretaceous - Hornerstown Late Cretaceous/Early Palaeocene) - charadriiform?
  • Palaeotringa (Hornerstown Late Cretaceous?) - charadriiform?
  • Telmatornis (Navesink Late Cretaceous?) - charadriiform? gruiform?
  • Scaniornis - phoenicopteriform?
  • Zhylgaia - presbyornithid?
  • Dakotornis
  • "Graculavidae" gen. et sp. indet. (Gloucester County, USA)

Other wader- or gull-like birds incertae sedis, which may or may not be Charadriiformes, are:

• Ceramornis (Lance Creek Late Cretaceous)
• "Cimolopteryx" (Lance Creek Late Cretaceous)
• Palintropus (Lance Creek Late Cretaceous)
• Torotix (Late Cretaceous)
• Volgavis (Early Paleocene of Volgograd, Russia)
• Eupterornis (Paleocene of France)
• Neornithes incerta sedis (Late Paleocene/Early Eocene of Ouled Abdoun Basin, Morocco)^[11]
• Fluviatitavis (Early Eocene of Silveirinha, Portugal)

Evolution of parental care in Charadriiformes

Shorebirds pursue a larger diversity of parental care strategies than do most other avian orders. They therefore present an attractive set of examples to support the understanding of the evolution of parental care in avians generally.^[12] The ancestral avian most likely had a female parental care system.^[13] The shorebird ancestor specifically evolved from a bi-parental care system, yet the species within the clade Scolopacidae evolved from a male parental care system. These transitions might have occurred for several reasons. Brooding density is correlated with male parental care. Male care systems in birds are shown to have a very low breeding density while female care systems in birds have a high breeding density. (Owens 2005). Certain rates of male and female mortality, male and female egg maturation rate, and egg death rate have been associated with particular systems as well.^[14] It has also been shown that sex role reversal is motivated by the male-biased adult sex ratio.^[15] The reason for such diversity in shorebirds, compared to other birds, has yet to be understood.

See also

• List of Charadriiformes by population

Footnotes

1. Fain & Houde (2004)
2. Ericson et al. (2003), Paton et al. (2003), Thomas et al. (2004a,b), van Tuinen et al. (2004), Paton & Baker (2006)
3. John, Boyd. "Charadriiformes". jboyd.net. Retrieved 2017-07-16.
4. van Tuinen et al. (2004), Paton & Baker (2006)
5. Baker, Allan J.; Yatsenko, Yuri; Tavares, Erika Sendra (2012). "Eight independent nuclear genes support monophyly of the plovers: The role of mutational variance in gene trees". Molecular Phylogenetics and Evolution. 65 (2): 631–641. doi:10.1016/j.ympev.2012.07.018. PMID 22842291.
6. Case, J. A. and C. P. Tambussi. 1999. Maastrichtian record of neornithine birds in Antarctica: comments on a Late Cretaceous radiation
7. Proximal right humerus (MNZ S42416) and proximal left carpometacarpi (MNZ S42415, S42435) of a bird the size of a red-necked stint: Worthy et al. (2007)
8. Several wing and thorax bones of a bird the size of a double-banded plover: Worthy et al. (2007)
9. Premaxillae (MNZ S42681, S42736) and proximal right scapula (MNZ S41058) of a bird apparently similar to the black-billed gull but almost the size of a kelp gull: Worthy et al. (2007)
10. Gál et al. (1998-99)
11. A wading bird the size of a white stork (Ciconia ciconia): Bourdon (2005)
12. Thomas, G. H., T. Székely and J.D. Reynolds. 2007. Sexual conflict and the evolution of breeding systems in shorebirds. Advances in the Study of Behavior. 37: 279–342.
13. Tullberg, B. S., M. Ah–King and H. Temrin. 2002. Phylogenetic reconstruction of parental–care systems in the ancestors of birds. Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences. 357: 251–257.
14. Klug, H., M. B. Bonsall, and S.H Alonzo. 2013. Sex differences in life history drive evolutionary transitions among maternal, paternal, and bi‐parental care. Ecology and Evolution. 3: 792–806.
15. Liker, A., R. P. Freckleton, and T. Székely. 2013. The evolution of sex roles in birds is related to adult sex ratio. Nature Communications. 4: 1587.

References

• Bourdon, Estelle (2006): L'avifaune du Paléogène des phosphates du Maroc et du Togo: diversité, systématique et apports à la connaissance de la diversification des oiseaux modernes (Neornithes) ["Paleogene avifauna of phosphates of Morocco and Togo: diversity, systematics and contributions to the knowledge of the diversification of the Neornithes"]. Doctoral thesis, Muséum national d'histoire naturelle [in French]. HTML abstract
• Ericson, Per G.P.; Envall, I.; Irestedt, M. & Norman, J.A. (2003): Inter-familial relationships of the shorebirds (Aves: Charadriiformes) based on nuclear DNA sequence data. BMC Evol. Biol. 3: 16. doi:10.1186/1471-2148-3-16 PDF fulltext
• Fain, Matthew G. & Houde, Peter (2004): Parallel radiations in the primary clades of birds. Evolution 58(11): 2558–2573. doi:10.1554/04-235 PMID 15612298 PDF 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
• Klug, H., M. B. Bonsall, and S.H Alonzo. 2013. Sex differences in life history drive evolutionary transitions among maternal, paternal, and bi‐parental care. Ecology and Evolution. 3: 792–806.
• Liker, A., R. P. Freckleton, and T. Székely. 2013. The evolution of sex roles in birds is related to adult sex ratio. Nature Communications. 4: 1587.
• Owens, I.P. 2002. Male–only care and classical polyandry in birds: phylogeny, ecology and sex differences in remating opportunities. Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences. 357: 283–293.
• Paton, Tara A. & Baker, Allan J. (2006): Sequences from 14 mitochondrial genes provide a well-supported phylogeny of the Charadriiform birds congruent with the nuclear RAG-1 tree. Mol. Phylogenet. Evol. 39(3): 657–667. doi:10.1016/j.ympev.2006.01.011 PMID 16531074 (HTML abstract)
• Paton, T.A.; Baker, A.J.; Groth, J.G. & Barrowclough, G.F. (2003): RAG-1 sequences resolve phylogenetic relationships within charadriiform birds. Mol. Phylogenet. Evol. 29: 268–278. doi:10.1016/S1055-7903(03)00098-8 PMID 13678682 (HTML abstract)
• Székely, T and J.D. Reynolds. 1995. Evolutionary transitions in parental care in shorebirds. Proceedings of the Royal Society of London. Series B: Biological Sciences. 262: 57–64.
• Thomas, G. H., T. Székely and J.D. Reynolds. 2007. Sexual conflict and the evolution of breeding systems in shorebirds. Advances in the Study of Behavior. 37: 279–342.
• Thomas, Gavin H.; Wills, Matthew A. & Székely, Tamás (2004a): Phylogeny of shorebirds, gulls, and alcids (Aves: Charadrii) from the cytochrome-b gene: parsimony, Bayesian inference, minimum evolution, and quartet puzzling. Mol. Phylogenet. Evol. 30(3): 516–526. doi:10.1016/S1055-7903(03)00222-7 (HTML abstract)
• Thomas, Gavin H.; Wills, Matthew A. & Székely, Tamás (2004): A supertree approach to shorebird phylogeny. BMC Evol. Biol. 4: 28. doi:10.1186/1471-2148-4-28 PMID 15329156 PDF fulltext Supplementary Material
• Tullberg, B. S., M. Ah–King and H. Temrin. 2002. Phylogenetic reconstruction of parental–care systems in the ancestors of birds. Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences. 357: 251–257.
• van Tuinen, Marcel; Waterhouse, David & Dyke, Gareth J. (2004): Avian molecular systematics on the rebound: a fresh look at modern shorebird phylogenetic relationships. J. Avian Biol. 35(3): 191–194. doi:10.1111/j.0908-8857.2004.03362.x PDF fulltext
• 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)