New World vulture
|New World vultures|
|Approximate Cathartidae range map
Yellow – Summer-only range of turkey vulture
The New World vulture or condor family Cathartidae contains seven species in five genera, all but one of which are monotypic. It includes five vultures and two condors found in warm and temperate areas of the Americas. The "New World" vultures were widespread in both the Old World and North America during the Neogene.
New World vultures do not form a monophyletic clade with the superficially similar family of Old World vultures, but similarities between the two groups are due to convergent evolution. Many now consider them to be in their own order Cathartiformes, closely related to, but distinct from, Old World vultures and allies (Accipitriformes).
Vultures are scavenging birds, feeding mostly from carcasses of dead animals without apparent ill effects. Bacteria in the food source, pathogenic to other vertebrates, dominate the vulture’s gut flora, and vultures benefit from the bacterial breakdown of carrion tissue. New World vultures have a good sense of smell, whereas Old World vultures find carcasses exclusively by sight. A particular characteristic of many vultures is a bald head, devoid of feathers.
Taxonomy and systematics
The New World vultures comprise seven species in five genera. The genera are Coragyps, Cathartes, Gymnogyps, Sarcoramphus, and Vultur. Of these, only Cathartes is not monotypic. The family's scientific name, Cathartidae, comes from cathartes, Greek for "purifier". Although New World vultures have many resemblances to Old World vultures they are not very closely related. Rather, they resemble Old World vultures because of convergent evolution.
New World vultures were traditionally placed in a family of their own in the Falconiformes. However, in the late 20th century some ornithologists argued that they are more closely related to storks on the basis of karyotype, morphological, and behavioral data. Thus some authorities placed them in the Ciconiiformes with storks and herons; Sibley and Monroe (1990) even considered them a subfamily of the storks. This was criticized, and an early DNA sequence study was based on erroneous data and subsequently retracted. There was then an attempt to raise the New World vultures to the rank of an independent order, Cathartiformes not closely associated with either the birds of prey or the storks and herons.
However, recent multi-locus DNA studies on the evolutionary relationships between bird groups indicate that New World vultures are related to the other birds of prey, excluding the Falconidae which are distantly related to other raptors, and are not close to storks. In this analysis, the New World vultures should be part of a new order Accipitriformes instead, or perhaps as part of an order (Cathartiformes) closely related to, but distinct from, other birds of prey (besides falcons). New World vultures are a sister group to Accipitriformes when the latter is viewed as a group consisting of Accipitridae, the osprey and secretarybird. Both groups are basal members of the recently recognized clade Afroaves.
|Common and binomial names||Image||Description||Range|
|South America and north to US|
|Throughout the Americas to southern Canada|
|Lesser yellow-headed vulture
|South America and north to Mexico|
|Greater yellow-headed vulture
|Amazon Basin of tropical South America|
|California, and formerly widespread in the mountains of western North America.|
|Southern Mexico to northern Argentina|
Extinct species and fossils
The fossil history of the Cathartidae is complex, and many taxa that may possibly have been New World vultures have at some stage been treated as early representatives of the family. There is no unequivocal European record from the Neogene.
It is clear that the Cathartidae had a much higher diversity in the Plio-Pleistocene, rivalling the current diversity of Old World vultures and their relatives in shapes, sizes, and ecological niches. Extinct taxa are:
- Diatropornis ("European vulture") Late Eocene/Early Oligocene –? Middle Oligocene of France
- Phasmagyps Chadronian of Colorado.
- Cathartidae gen. et sp. indet. (Late Oligocene of Mongolia)
- Brasilogyps Late Oligocene – Early Miocene of Brazil
- Hadrogyps ("American dwarf vulture") Middle Miocene of SW North America
- Cathartidae gen. et sp. indet. Late Miocene/Early Pliocene of Lee Creek Mine, USA
- Pliogyps ("Miocene vulture") Late Miocene – Late Pliocene of S North America
- Perugyps ("Peruvian vulture)" Pisco Late Miocene/Early Pliocene of SC Peru
- Dryornis ("Argetinean vulture") Early–Late? Pliocene of Argentina; may belong to modern genus Vultur
- Cathartidae gen. et sp. indet. (Middle Pliocene of Argentina
- Aizenogyps ("South American vulture") Late Pliocene of SE North America
- Breagyps ("long-legged vulture)" Late Pleistocene of SW North America
- Geronogyps Late Pleistocene of Argentina and Peru
- Gymnogyps varonai late Quaternary of Cuba 
- Wingegyps ("Amazonian vulture") Late Pleistocene of Brazil 
- Cathartidae gen. et sp. indet. (Cuba)
New World vultures are generally large, ranging in length from the lesser yellow-headed vulture at 56–61 centimeters (22–24 inches) up to the California and Andean condors, both of which can reach 120 centimeters (48 inches) in length and weigh 12 or more kilograms (26 or more pounds). Plumage is predominantly black or brown, and is sometimes marked with white. All species have featherless heads and necks. In some, this skin is brightly colored, and in the king vulture it is developed into colorful wattles and outgrowths.
All New World vultures have long, broad wings and a stiff tail, suitable for soaring. They are the best adapted to soaring of all land birds. The feet are clawed but weak and not adapted to grasping. The front toes are long with small webs at their bases. No New World vulture possesses a syrinx, the vocal organ of birds. Therefore the voice is limited to infrequent grunts and hisses.
The beak is slightly hooked and is relatively weak compared with those of other birds of prey. This is because it is adapted to tear the weak flesh of partially rotted carrion, rather than fresh meat. The nostrils are oval and are set in a soft cere. The nasal passage is not divided by a septum (it is "perforate"), so that when looking from the side, one can see through the beak. The eyes are prominent, and, unlike those of eagles, hawks, and falcons, they are not shaded by a brow bone. Members of Coragyps and Cathartes have a single incomplete row of eyelashes on the upper lid and two rows on the lower lid, while Gymnogyps, Vultur, and Sarcoramphus lack eyelashes altogether.
New World vultures have the unusual habit of urohidrosis, or defecating on their legs to cool them evaporatively. As this behavior is also present in storks, it is one of the arguments for a close relationship between the two groups.
Distribution and habitat
New World vultures are restricted to the western hemisphere. They can be found from southern Canada to South America. Most species are mainly resident, but the turkey vulture populations breeding in Canada and the northern US migrate south in the northern winter. New World vultures inhabit a large variety of habitats and ecosystems, ranging from deserts to tropical rainforests and at heights of sea level to mountain ranges, using their highly adapted sense of smell to locate carrion. These species of birds are also occasionally seen in human settlements, perhaps emerging to feed upon the food sources provided from roadkills.
Behaviour and ecology
All living species of New World vultures and condors are scavengers. Their diet is overwhelmingly composed of carrion, and they are commonly seen in carcasses. Other additions to the diet include fruit (especially rotten fruit) and garbage. An unusual characteristic of the species in genus Cathartes is a highly developed sense of smell, which they use to find carrion. They locate carrion by detecting the scent of ethyl mercaptan, a gas produced by the bodies of decaying animals. The olfactory lobe of the brains in these species, which is responsible for processing smells, is particularly large compared to that of other animals. Other species, such as the American black vulture and the king vulture, have weak senses of smell and find food only by sight, sometimes by following Cathartes vultures and other scavengers. The head and neck of New World vultures are featherless as an adaptation for hygiene; this lack of feathers prevents bacteria from the carrion it eats from ruining its feathers and exposes the skin to the sterilizing effects of the sun.
Tolerance to bacterial toxins in decaying meat
Vultures posess "a ferociously acidic digestive system and intestines loaded with two fiendish kinds of bacteria". This is the result of a study in which the microbial community or microbiome of the facial skin and the large intestine of 50 (turkey and black) vultures were characterized. Facial flora and gut flora overlapped somewhat, but facial flora was much more diverse than the gut flora, in opposition to other vertebrates. Two anaerobic faecal bacteria groups that are pathogenic in other vertebrates stood out: Clostridia and Fusobacteria. They were remarkably common in the gut with Clostridia DNA sequence counts between 26% and 85% relative to total sequence counts, and Fusobacteria between 0.2% and 54% in black vultures and a bit more at 2% to 69% relative to total counts in turkey vultures. Unexpectedly, both Clostridia (7% to 40%) and Fusobacteria (0.2% to 23%) were also present on the facial skin samples, which are exposed to air. It is assumed that vultures acquire these when they insert their heads into the body cavities of decaying prey, and that their gut predominance results from Clostridia and Fusobacteria outcompeting other bacterial groups. Genes that encode tissue-degrading enzymes and toxins associated with Clostridium perfringens found in the vulture gut metagenome support the hypothesis, that vultures benefit from the bacterial breakdown of carrion while tolerating bacterial toxins.
New World vultures and condors do not build nests, but lay eggs on bare surfaces. On average one to three eggs are laid, depending on the species. Chicks are naked on hatching and later grow down. Like most birds the parents feed the young by regurgitation. The young are altricial, fledging in 2 to 3 months.
Status and conservation
The California condor is critically endangered. It formerly ranged from Baja California to British Columbia, but by 1937 was restricted to California. In 1987, all surviving birds were removed from the wild into a captive breeding program to ensure the species' survival. In 2005, there were 127 Californian condors in the wild. As of October 31, 2009 there were 180 birds in the wild. The Andean condor is near threatened. The American black vulture, turkey vulture, lesser yellow-headed vulture, and greater yellow-headed vulture are listed as species of Least Concern by the IUCN Red List. This means that populations appear to remain stable, and they have not reached the threshold of inclusion as a threatened species, which requires a decline of more than 30 percent in ten years or three generations. The king vulture is also listed as Least Concern, although there is evidence of a decline in the population.
The American black vulture and the king vulture appear in a variety of Maya hieroglyphs in Mayan codices. The king vulture is one of the most common species of birds represented. Its glyph is easily distinguishable by the knob on the bird's beak and by the concentric circles that represent the bird's eyes. It is sometimes portrayed as a god with a human body and a bird head. According to Mayan mythology, this god often carried messages between humans and the other gods. It is also used to represent Cozcaquauhtli, the thirteenth day of the month in the Mayan calendar. In Mayan codices, the American black vulture is normally connected with death or shown as a bird of prey, and its glyph is often depicted attacking humans. This species lacks the religious connections that the king vulture has. While some of the glyphs clearly show the American black vulture's open nostril and hooked beak, some are assumed to be this species because they are vulture-like and painted black, but lack the king vulture's knob.
- Jarvis, E. D.; Mirarab, S.; Aberer, A. J.; Li, B.; Houde, P.; Li, C.; Ho, S. Y. W.; Faircloth, B. C.; Nabholz, B.; Howard, J. T.; Suh, A.; Weber, C. C.; Da Fonseca, R. R.; Li, J.; Zhang, F.; Li, H.; Zhou, L.; Narula, N.; Liu, L.; Ganapathy, G.; Boussau, B.; Bayzid, M. S.; Zavidovych, V.; Subramanian, S.; Gabaldon, T.; Capella-Gutierrez, S.; Huerta-Cepas, J.; Rekepalli, B.; Munch, K. et al. (2014-12-12). "Whole-genome analyses resolve early branches in the tree of life of modern birds". Science 346 (6215): 1320–1331. doi:10.1126/science.1253451.
- Myers (2008)
- Brookes (2006)
- Phillips (2000)
- Sibley and Ahlquist (1991)
- de Boer (1975)
- Ligon (1967)
- König (1982)
- Griffiths (1994)
- Fain & Houde (2004)
- Avise (1994)
- Brown (2009)
- Cracraft et al. (2004)
- Gibb et al. (2007)
- Ericson et al. (2006)
- Hackett et al. (2008)
- Griffiths, C. S.; Barrowclough, G. F.; Groth, J. G.; Mertz, L. A. (2007-11-06). "Phylogeny, diversity, and classification of the Accipitridae based on DNA sequences of the RAG-1 exon". Journal of Avian Biology 38 (5): 587–602. doi:10.1111/j.2007.0908-8857.03971.x.
- BirdLife International (2009a)
- BirdLife International (2009)
- Mayr (2006)
- Emslie (1988)
- Wetmore, A. (1927). "Fossil Birds from the Oligocene of Colorado". Proceedings of the Colorado Museum of Natural History 7 (2): 1–14.
- Stucchi (2005)
- Suárez (2003)
- Alvarenga (2004).
- Suarez (2004)
- Zim et al. (2001)
- Reed (1914)
- Ryser & Ryser (1985)
- Krabbe (1990)
- Feduccia (1999)
- Kemp and Newton (2003)
- Howell and Webb (1995)
- Terres (1991)
- Allaby (1992)
- Fisher (1942)
- Harris (2009)
- Farmer (2008)
- Snyder (2006)
- Stone (1992)
- Will Dunham (26 November 2014). "Gut check: how vultures dine on rotting flesh, and like it". Reuters (Thomson Reuters). Retrieved 27 November 2014.
- Michael Roggenbuck, Ida Bærholm Schnell,Nikolaj Blom et al (25 November 2014). "The microbiome of New World vultures". Nature Communications 5 (5498). doi:10.1038/ncomms6498.
- "San Diego Zoo's Animal Bytes: California Condor". The Zoological Society of San Diego's Center for Conservation and Research for Endangered Species. Retrieved 2009-12-29.
- BirdLife International (2001)
- Tozzer (1910)
- Allaby, Michael (1992). The Concise Oxford Dictionary of Zoology. Oxford: Oxford University Press ISBN 0-19-286093-3, p. 348
- Alvarenga, H. M F. & S. L. Olson. (2004). "A new genus of tiny condor from the Pleistocene of Brazil (Aves: Vulturidae)." Proceedings of the Biological Society of Washington 117(1) 1 9
- American Ornithologists' Union (2009) Check-list of North American Birds, Tinamiformes to Falconiformes 7th Edition. AOU. Retrieved 6 October 2009
- American Ornithologists' Union (2010) Check-list of North American Birds, Tinamiformes to Falconiformes 7th Edition. AOU. Retrieved 3 August 2010
- Avise, J. C.; Nelson, W. S. & Sibley, C. G. (1994) "DNA sequence support for a close phylogenetic relationship between some storks and New World vultures" Proc. Natl. Acad. Sci. USA 91(11): 5173–5177. doi:10.1073/pnas.91.11.5173 (PDF). Erratum, PNAS 92(7); 3076 (1995). doi:10.1073/pnas.92.7.3076b
- BirdLife International (2004). 2001 Categories & Criteria (version 3.1). International Union for Conservation of Nature and Natural Resources. Retrieved 9 September 2007.
- BirdLife International (2009). Vultur gryphus. In: IUCN 2008. IUCN Red List of Threatened Species. Retrieved 6 October 2009.
- BirdLife International (2009a). Gymnogyps californianus. In: IUCN 2008. IUCN Red List of Threatened Species. Retrieved 6 October 2009.
- Brookes, Ian (editor-in-chief) (2006). The Chambers Dictionary, ninth edition. Edinburgh: Chambers. ISBN 0-550-10185-3. p. 238
- Brown J. W. & D. P. Mindell (2009) "Diurnal birds of prey (Falconiformes)" pp. 436–439 in Hedges S. B. and S. Kumar, Eds. (2009) The Timetree of Life Oxford University Press. ISBN 019953503
- de Boer, L. E. M.(1975) "Karyological heterogeneity in the Falconiformes (Aves)" Cellular and Molecular Life Sciences 31(10): 1138–1139. doi:10.1007/BF02326755 PMID 1204722
- Campbell, Kenneth E. Jr. & Tonni, E. P. (1983): "Size and locomotion in teratorns" (PDF) Auk 100(2): 390–403
- Cracraft, J., F. K. Barker, M. Braun, J. Harshman, G. J. Dyke, J. Feinstein, S. Stanley, A. Cibois, P. Schikler, P. Beresford, J. García-Moreno, M. D. Sorenson, T. Yuri, and D. P. Mindell. (2004) "Phylogenetic relationships among modern birds (Neornithes): toward an avian tree of life." pp. 468–489 in Assembling the tree of life (J. Cracraft and M. J. Donoghue, eds.). Oxford University Press, New York.
- Emslie, Steven D. (1988) "An early condor-like vulture from North America" The Auk 105:3 529–535
- Ericson, Per G. P.; Anderson, Cajsa L.; Britton, Tom; Elżanowski, Andrzej; Johansson, Ulf S.; Kallersjö, Mari; Ohlson, Jan I.; Parsons, Thomas J.; Zuccon, Dario & Mayr, Gerald (2006): Diversification of Neoaves: integration of molecular sequence data and fossils. Biology Letters, in press. doi:10.1098/rsbl.2006.0523 PMID 17148284
- Farmer A, Francl, K (2008) Cathartes aura University of Michigan Animal Diversity Web. Retrieved 8 October 2009
- Feduccia, J. Alan. (1999) The Origin and Evolution of Birds Yale University Press ISBN 0-226-05641-4 p. 300
- Fisher, Harvey I. (1942) "The Pterylosis of the Andean Condor" Condor 44(1): 30–32.
- Gibb, G. C., O. Kardailsky, R. T. Kimball, E. L. Braun, and D. Penny. 2007. Mitochondrial genomes and avian phylogeny: complex characters and resolvability without explosive radiations. Molecular Biology Evolution 24: 269–280.
- Harris, Tim (2009). Complete Birds Of The World. Washington D.C: National Geographic Society. ISBN 978-1-4262-0403-6. p. 72
- Hackett, S. J.; Kimball, R. T.; Reddy, S.; Bowie, R. C. K.; Braun, E. L.; Braun, M. J.; Chojnowski, J. L.; Cox, W. A.; Han, K. -L.; Harshman, J.; Huddleston, C. J.; Marks, B. D.; Miglia, K. J.; Moore, W. S.; Sheldon, F. H.; Steadman, D. W.; Witt, C. C.; Yuri, T. (2008-06-27). "A Phylogenomic Study of Birds Reveals Their Evolutionary History". Science 320 (5884): 1763–1768. doi:10.1126/science.1157704. PMID 18583609. Retrieved 2011-05-26.
- Howell, Steve N.G., and Sophie Webb (1995). A Guide to the Birds of Mexico and Northern Central America. New York: Oxford University Press ISBN 0-19-854012-4, p. 174
- Kemp, Alan, and Ian Newton (2003): New World Vultures. In Christopher Perrins, ed., The Firefly Encyclopedia of Birds. Firefly Books. ISBN 1-55297-777-3. p. 146
- Krabbe, Niels & Fjeldså, Jon. 1990: Birds of the High Andes. Apollo Press ISBN 87-88757-16-1 p. 88
- Ligon, J. D. (1967): Relationships of the cathartid vultures. Occasional Papers of the Museum of Zoology, University of Michigan 651: 1–26.
- Mayr, G. (2006). "A new raptorial bird from the Middle Eocene of Messel, Germany." Historical Biology 18(2): 95–102
- Myers, P., R. Espinosa, C. S. Parr, T. Jones, G. S. Hammond, and T. A. Dewey. (2008) Family Cathartidae University of Michigan Animal Diversity Web Retrieved 5 October 2009
- Phillips, Steven J, Comus, Patricia Wentworth (Arizona-Sonora Desert Museum) (2000) A natural history of the Sonoran Desert University of California Press ISBN 0-520-21980-5 p,377
- Reed, Chester Albert (1914): The bird book: illustrating in natural colors more than seven hundred North American birds, also several hundred photographs of their nests and eggs. University of Wisconsin. p. 198
- Remsen, J. V., Jr., C. D. Cadena, A. Jaramillo, M. Nores, J. F. Pacheco, M. B. Robbins, T. S. Schulenberg, F. G. Stiles, D. F. Stotz, and K. J. Zimmer. A classification of the bird species of South America. American Ornithologists' Union.
- Ryser Fred A. & A. Ryser, Fred Jr. 1985: Birds of the Great Basin: A Natural History. University of Nevada Press. ISBN 0-87417-080-X p. 211
- Sibley, Charles G. and Burt L. Monroe (1990) Distribution and Taxonomy of the Birds of the World. Yale University Press. ISBN 0-300-04969-2
- Sibley, Charles G., and Jon E. Ahlquist (1991) Phylogeny and Classification of Birds: A Study in Molecular Evolution. Yale University Press. ISBN 0-300-04085-7
- Snyder, Noel F. R. & Snyder, Helen (2006). Raptors of North America: Natural History and Conservation. Voyageur Press. ISBN 0-7603-2582-0 p. 40
- Stone, Lynn M. (1992) Vultures Rourke Publishing Group ISBN 0-86593-193-3 p. 14
- (Spanish) Stucchi, Marcelo; Emslie Steven D. (2005) "Un Nuevo Cóndor (Ciconiiformes, Vulturidae) del Mioceno Tardío-Plioceno Temprano de la Formación Pisco, Perú." The Condor 107:(1) 107 113 doi:10.1650/7475
- Suárez, W.; Emslie, S.D. (2003). "New fossil material with a redescription of the extinct condor Gymnogyps varonai (Arredondo, 1971) from the Quaternary of Cuba (Aves: Vulturidae)". Proceedings of the Biological Society of Washington 116 (1): 29–37.
- Suarez, William (2004) "The identity of the fossil raptor of the genus Amplibuteo (Aves: Accipitridae) from the Quaternary of Cuba" Caribbean Journal of Science 40: (1) 120 125
- Terres, J. K. & National Audubon Society (1991). The Audubon Society Encyclopedia of North American Birds. Reprint of 1980 edition. ISBN 0-517-03288-0 p 957
- Tozzer, Alfred Marston & Allen, Glover Morrill (1910). Animal Figures in the Maya Codices. Harvard University Plates 17 & 18
- Wink, M. (1995): Phylogeny of Old and New World vultures (Aves: Accipitridae and Cathartidae) inferred from nucleotide sequences of the mitochondrial cytochrome b gene. Zeitschrift für Naturforschung 50 (11–12): 868–882.
- Zim, Herbert Spencer; Robbins, Chandler S.; Bruun, Bertel (2001) Birds of North America: A Guide to Field Identification Golden Publishing. ISBN 1-58238-090-2
|Wikimedia Commons has media related to Cathartidae.|
- New World Vulture videos, photos and sounds on the Internet Bird Collection
- New World Vulture sounds on xeno-canto.org
- New World Vulture photos on beautyofbirds.com