Jump to content

Phorusrhacidae

From Wikipedia, the free encyclopedia
(Redirected from Terror Bird)
"Terror Bird" redirects here. For the studio album, see Terrorbird.
Phorusrhacidae
Temporal range: Middle Eocene – Late Pleistocene[1][2]
~43–0.1 Ma
Reconstructed skeleton of Titanis walleri, Florida Museum of Natural History
Scientific classification Edit this classification
Domain: Eukaryota
Kingdom: Animalia
Phylum: Chordata
Class: Aves
Order: Cariamiformes
Superfamily: †Phorusrhacoidea
Ameghino, 1889
Family: †Phorusrhacidae
Ameghino, 1889[3]
Type species
†Phorusrhacos longissimus
Ameghino, 1887
Subfamilies
  • †Phsyornithinae
  • †Mesembriornithinae
  • †Patagornithinae
  • †Phorusrhacinae
  • †Psilopterinae
Synonyms
Family synonymy
  • Pelecyornidae Ameghino, 1891
  • Brontornithidae Moreno & Mercerat, 1891
  • Darwinornithidae Moreno & Mercerat, 1891
  • Stereornithidae Moreno & Mercerat, 1891
  • Patagornithidae Mercerat, 1897
  • Hermosiornidae Rovereto, 1914
  • Psilopteridae Dolgopol de Saez, 1927
  • Devincenziidae Kraglievich, 1932
  • Mesembriorniidae Kraglievich, 1932

Phorusrhacids, colloquially known as terror birds, are an extinct family of large carnivorous, mostly flightless birds[a] that were among the largest apex predators in South America during the Cenozoic era. Their definitive fossil records range from the Middle Eocene to the Late Pleistocene around 43 to 0.1 million years ago,[1][2] though some specimens suggest that they were present since the Early Eocene.

They ranged in height from 1 to 3 m (3 to 10 ft). One of the largest specimens from the Early Pleistocene of Uruguay, possibly belonging to Devincenzia, would have weighed up to 350 kilograms (770 lb).[5][6] Their closest modern-day relatives are believed to be the 80-centimetre-tall (31 in) seriemas. Titanis walleri, one of the larger species, is known from Texas and Florida in North America. This makes the phorusrhacids the only known large South American predator to migrate north in the Great American Interchange that followed the formation of the Isthmus of Panama land bridge (the main pulse of the interchange began about 2.6 Ma ago; Titanis at 5 Ma was an early northward migrant).[7]

It was once believed that T. walleri became extinct in North America around the time of the arrival of humans,[8] but subsequent datings of Titanis fossils provided no evidence for their survival after 1.8 Ma.[9] However, reports from Uruguay of new findings of phorusrachids such as a specimen of Psilopterus dating to 96,040 ± 6,300 years ago would imply that phorusrhacids survived in South America until the late Pleistocene.[b]

Phorusrhacids may have even made their way into Africa and Europe, if the genus Lavocatavis from Algeria and Eleutherornis from France and Switzerland are included.[10][11] However, the taxonomic placement of both taxa within phorusrhacids are considered highly questionable, and their remains are too fragmentary to be included in phylogenetic analyses.[12][13][14] Possible specimens have also been discovered from the La Meseta Formation of Seymour Island, Antarctica, suggesting that this group had a wider geographical range in the Paleogene.[15]

The closely related bathornithids occupied a similar ecological niche in North America across the Eocene to Early Miocene; some, like Paracrax, were similar in size to the largest phorusrhacids.[16][17] At least one analysis recovers Bathornis as sister taxa to phorusrhacids, on the basis of shared features in the jaws and coracoid,[18] though this has been seriously contested, as these might have evolved independently for the same carnivorous, flightless lifestyle.[19]

Description

[edit]
Phorusrhacinae skulls compared

The neck can be divided into three main regions. In the higher regions of the neck, the phorusrhacid has bifurcate neural spines (BNS), while it has high neural spines in its lower regions. This suggests that the phorusrhacid had a highly flexible and developed neck allowing it to carry its heavy head and strike with terrifying speed and power. Although the phorusrhacid externally looks like it has a short neck, its flexible skeletal neck structure proves that it could expand farther beyond the expected reach and intimidate its prey using its height, allowing it to strike more easily. Once stretched out into its full length in preparation for a downward strike, its developed neck muscles and heavy head could produce enough momentum and power to cause fatal damage to the terror bird's prey.[20]

Kelenken guillermoi, from the Langhian stage of the Miocene epoch, some 15 million years ago, discovered in the Collón Curá Formation in Patagonia in 2006, represents the largest bird skull yet found. The fossil has been described as being a 71-centimetre (28 in), nearly intact skull. The beak is roughly 46 cm (18 in) long and curves in a hook shape that resembles an eagle's beak. Most species described as phorusrhacid birds were smaller, 60–90 cm (2.0–3.0 ft) tall, but the new fossil belongs to a bird that probably stood about 3 m (9.8 ft) tall. Scientists theorize that the large terror birds were extremely nimble and quick runners, able to reach speeds of 48 km/h (30 mph).[21] Examination of phorusrhacid habitats also indicates that phorusrhacids may have presented intense competition to predatory metatherian sparassodonts such as borhyaenids and thylacosmilids, causing the mammalian predators to choose forested habitats to avoid the more successful and aggressive avian predators on the open plains.[22]

The feet of the phorusrhacids had four toes, the first of which, known as the hallux, was reduced and did not touch the ground, while the others, corresponding to the second, third and fourth toes, were kept on the ground. Analysis of the resistance of the toes based on biomechanical models of curved beams, in particular of the second toe and its nail claw, indicate that it was modified into a "sickle claw" and was relatively uniform in various species and said claw would be relatively curved and large, which implies the need to keep it elevated to avoid wear or breakage due to contact with the ground, which would be achieved with a well-developed extensor tubercle and soft tissue pads on the fingers. The second toe, which was shorter and had fewer phalanges, also had more resistance and would make it easier to hold the claw off the ground and retain prey, a compromise with its predatory function and movement on the run, as occurs with modern seriemas, although to a lesser degree of specialization than dromaeosaurid dinosaurs.[23] This is further supported by footprints from the Late Miocene of the Río Negro Formation, showcasing a trackway made by a mid-to-large sized terror bird with functionally didactyl footprints, the inner toe with the sickle claw raised mostly off the ground akin to their Mesozoic counterparts.[24]

Skull structure

[edit]
CT scan of the skull of P 14357, holotype of Andalgalornis ferox in the collections of the Field Museum of Natural History
Phorusrhacid skulls
Comparison of different phorusrhacid skulls

In the past, these birds were thought to have high beaks, round orbits, and vaulted braincases[25] though there was never enough empirical evidence to support this. However, new fossils have been discovered in Comallo, Argentina. These skulls reveal that the terror bird has a triangular dorsal view, a rostrum that is hooked and more than half the length of the actual skull, and a more compact caudal portion. The external nares and antorbital fenestras (areas found in the nose) were found to be more square than triangular. These all contribute to a skull that is more rectangular in view rather than triangular.[25] The structure of the fossils also suggest that these birds may have been swifter than originally thought.[25]

A skull from a smaller subspecies of this bird was also found recently. With this fossil, it was found that the internal structure of the beak is hollow and reinforced with thin-walled trabeculae. There is also an absence of both zona flexoria palatina and zona flexoria arcus jugalis, which are key features that relate to the evolution of cranial akinesis. The discovery of this skull allows for the establishment of primary osteological homologies, which are useful in comparative anatomy, functional morphology, and phylogenetic studies.[26]

Palaeobiology

[edit]
Restoration of Andalgalornis

Most phorusrhacids were very fast runners. All members possessed a large, sharp beak, a powerful neck and sharp talons. However, even with these attributes, the phorusrhacids are often assumed to have preyed on relatively small animals (about the size of a rabbit) that could be dispatched with a minimum of struggle. This is because with the phorusrhacids' beak proportions, the jaw could not generate a great deal of bite force with which to kill the prey. This is disputable as many big-game hunting predators such as Smilodon, great white sharks and Allosaurus have weaker bite forces and often laterally weak skulls as adaptations towards, not away from, killing large prey, relying instead on the presence of a cutting edge, a wide gape made possible by the reduction of jaw musculature, and the driving force of the body or neck.[27][28] Since phorusrhacids share many of the same adaptations, such as a large, laterally flattened skull with a sharp-edged beak and powerful neck musculature, it is possible that they were specialized predators of relatively large prey.

The bones of the beak were tightly fused together, making the beak more resilient to force from the front to back direction, thus suggesting that it could cause a great amount of harm through pecking as opposed to side-to-side head movements like shaking prey. Generally speaking, it is thought that a terror bird would use its feet to injure prey by kicking it, and to hold the prey down and dispatch by pecking at it with its large beak. Larger prey may also have been attacked by pecking and kicking,[29] or by using the beak as a blade to strike at or slash vital organs.

Only known phorusrhacid trackway, named Rionegrina, which confirms that they held their second toe off the ground like seriemas and dromaeosaurs

It has been recently shown that at least some phorusrhacids like Andalgalornis, while very fast runners in a straight line, were poor at tight turns at speed, which contradicts the idea of phorusrhacids being agile predators of small prey.[30]

Diet

[edit]

All phorusrhacids are thought to have been carnivorous. The strong downwards curve from the tip of this beak suggests that it ripped the flesh from the body of other animals; many extant bird species with this feature are carnivorous. CT scans performed on the skull of a phorusrhacid reveal that the species would not have been able to shake its prey side to side, but rather exert significant downward force.[31] Florentino Ameghino claimed in a letter to Édouard Trouessart that he had specimens from Argentina of "petrified masses preserving skeletons of large rodents, Interatheriidae [small notoungulates] and even Proterotheriidae [deer-sized litopterns], with all their bones crushed and corroded, piled on with no apparent order and forming a nearly spherical mass with the skull in the center" that resembled giant owl pellets, suggesting that phorusrhacids may have swallowed their prey whole and regurgitated the indigestible parts similar to owls.[32][33] However, Ameghino never formally described these specimens and they have not yet been relocated, making it difficult to determine if they are phorusrhacid pellets.[33] Fossilized pellets from northwestern Argentina have also been suggested to pertain to small phorusrhacids like Procariama.[34]

Classification

[edit]

The etymology of the name Phorusrhacidae is based on the type genus Phorusrhacos. When first described by Florentino Ameghino in 1887, the etymology of Phorusrhacos was not given. Current thinking is that the name is derived from a combination of the Greek words "phoros", which means bearer or bearing, and "rhakos", which translates to wrinkles, scars or rents.[35] Researchers have compared Phorusrhacidae with the living families of Cariamidae and Sagittariidae, but their differences in body mass are too drastic and, thus, one cannot overly depend on these living families for answers.

During the early Cenozoic, after the extinction of the non-bird dinosaurs, mammals underwent an evolutionary diversification, and some bird groups around the world developed a tendency towards gigantism; this included the Gastornithidae, the Dromornithidae, the Palaeognathae, and the Phorusrhacidae.[36] Phorusrhacids are an extinct group within Cariamiformes, the only living members of which are the two species of seriemas in the family Cariamidae. While they are the most taxon-rich group within Cariamiformes, the interrelationships between phorusrhacids are unclear due to the incompleteness of their remains.[37] A lineage of related predatory birds, the bathornithids, occupied North America prior to the arrival of phorusrhacids, living from the Eocene to Miocene and filled a similar niche to phorusrhacids.[38] Only one genus belongs in the family, Bathornis, according to a 2016 analysis by paleontologist Gerald Mayr, who noted that Bathornis was more lightly built, with longer limbs proportionally and skulls more akin to those of Cariama.[39]

The red-legged seriema, the closest living relative of phorusrhacids

Phylogenetic analysis of Cariamiformes and their relatives according to Mayr (2016) in his redescription of Bathornis:[39] A 2024 study finds Bathornis as closer to seriemas than phorusrhacids were.[14]

Following the revision by Alvarenga and Höfling (2003), there are now 5 subfamilies, containing 14 genera and 18 species:[40] These species were the product of adaptive radiation.[41] The following classification is based on LaBarge, Garderner & Organ (2024), and taxa identified as incertae sedis were all excluded from phylogenetic analysis in their study (except for Brontornis):[14]

Family Phorusrhacidae

Reconstructed skeleton of Paraphysornis at the Museu Nacional, Rio de Janeiro

Alvarenga and Höfling did not include the Ameghinornithidae from Europe in the phorusrhacoids; these have meanwhile turned out to be more basal members of Cariamae.[48] Though traditionally considered as members of the Gruiformes, based on both morphological and genetic studies (the latter being based on the seriema[49]) Cariamiformes may belong to a separate group of birds, Australaves, and their closest living relatives, according to nuclear sequence studies, are a clade consisting of Falconidae, Psittaciformes and Passeriformes.[50][51]

The following cladogram follows the analysis of Degrange and colleagues, 2015:[47]

Phorusrhacidae 
Physornithinae
Phorusrhacinae
Patagornithinae

Extinction

[edit]

During the Miocene and early Pliocene epochs, there was an increase in the phorusrhacid population size in South America, suggesting that, in that time frame, the various species flourished as predators in the savanna environment.

With the emergence of the Isthmus of Panama 2.7 million years ago, carnivorous dogs, bears, and cats from North America were able to cross into South America, increasing competition.[52] (They had been preceded by procyonids as early as 7.3 million years ago.[7]) The population of phorusrhacids declined thereafter according to older hypotheses, suggesting that competition with newly arrived predators was a major contributor to their extinction.[53] Similar ideas have been considered for sparassodonts and for South America's terrestrial sebecid crocodilians.[54]

However, the role of competitive displacement in South American predator lineages has been questioned by some researchers.[55] The timing of turnover events and the decline of South American predators do not correlate well with the arrival of large carnivores like canids or sabretooths (although they do correlate well with the earlier-arriving procyonids, which evolved to large body size in South America, but these were omnivorous[56]), with native South American predator lineages (including most phorusrhacids and all sparassodonts and sebecids) dying out well before the arrival of most larger placental carnivores.[57] Bathornithids, which were similar in ecology and are likely close relatives of phorusrhacids, existed entirely within North America during part of the Cenozoic and competed successfully for a time with large carnivorans such as nimravids,[17] before becoming extinct in the Early Miocene, about 20 million years ago. The phorusrhacid Titanis expanded northward into southern North America during the Interchange and coexisted for several million years with large canids and big cats like Xenosmilus, before its extinction about 1.8 million years ago.

There were some suggestions that phorusrhacids, like the majority of Pleistocene megafauna, were killed off by human activity such as hunting or habitat change. This idea is no longer considered valid, as improved dating on Titanis specimens show that the last phorusrhacids went extinct over one million years before humans arrived.[9] However, several fossil finds of smaller forms have been described from the late Pleistocene of Uruguay in South America. Psilopterus may have been present until 96,040 ± 6,300 years ago (maximum age obtained from the bottom of the fossil-containing stratum), which would extend the existence of the smaller members of this group of avian predators considerably.[2] Another unidentified smaller type which may be a possible psilopterine[2] from the La Paz Local Fauna of Uruguay has also been dated to the late Pleistocene, perhaps 17,620 ± 100 years ago based on radiocarbon analysis using accelerator mass spectrometry (AMS) for the molar enamel samples of a proboscidean from the same site,[58] but the validity of this previous radiocarbon dating has been considered highly questionable due to the enamel's lack of collagen;[59] the tibia of Macrauchenia patachonica from the same site has been more precisely dated to a mean value of approximately 21,600 ± 1,000 years ago based on gamma spectrometry and radiocarbon dating.[60]

Notes

[edit]
  1. ^ It has been suggested that psilopterines like Psilopterus may have been able to fly briefly in a clumsy manner, primarily to reach the treetops for nesting and protection, on the basis of body mass estimates and hindlimb proportions being similar to those of certain birds like Psophia and Otis which often walk but are able to run and fly.[4][1]
  2. ^ To be specific, this is the maximum age obtained from the bottom of the fossil-containing stratum.[2]

References

[edit]
  1. ^ a b c Acosta Hospitaleche, C.; Jones, W. (2024). "Insights on the oldest terror bird (Aves, Phorusrhacidae) from the Eocene of Argentina". Historical Biology: An International Journal of Paleobiology: 1–9. doi:10.1080/08912963.2024.2304592. S2CID 267475903.
  2. ^ a b c d e Jones, W.; Rinderknecht, A.; Alvarenga, H.; Montenegro, F.; Ubilla, M. (2017). "The last terror birds (Aves, Phorusrhacidae): new evidence from the late Pleistocene of Uruguay". Paläontologische Zeitschrift. 92 (2): 365–372. doi:10.1007/s12542-017-0388-y. S2CID 134344096.
  3. ^ Ameghino, F (1889). "Contribuición al conocimiento de los mamíferos fósiles de la República Argentina" [Contribution to the knowledge of fossil mammals in the Argentine Republic]. Actas Academia Nacional Ciencias de Córdoba (in Spanish). 6: 1–1028.
  4. ^ Degrange, F.J. (2015). "Hind limb morphometry of terror birds (Aves, Cariamiformes, Phorusrhacidae): functional implications for substrate preferences and locomotor lifestyle". Earth and Environmental Science Transactions of the Royal Society of Edinburgh. 106 (4): 257–276. Bibcode:2015EESTR.106..257D. doi:10.1017/S1755691016000256. hdl:11336/44728.
  5. ^ a b Alvarenga, H. M. F.; Höfling, E. (2003). "Systematic revision of the Phorusrhacidae (Aves: Ralliformes)". Papéis Avulsos de Zoologia. 43 (4): 55–91. doi:10.1590/S0031-10492003000400001.
  6. ^ Blanco, Rudemar Ernesto; Jones, Washington W (2005). "Terror birds on the run: a mechanical model to estimate its maximum running speed". Proceedings of the Royal Society B: Biological Sciences. 272 (1574): 1769–1773. doi:10.1098/rspb.2005.3133. PMC 1559870. PMID 16096087.
  7. ^ a b Woodburne, M. O. (2010-07-14). "The Great American Biotic Interchange: Dispersals, Tectonics, Climate, Sea Level and Holding Pens". Journal of Mammalian Evolution. 17 (4): 245–264. doi:10.1007/s10914-010-9144-8. PMC 2987556. PMID 21125025.
  8. ^ Baskin, J. A. (1995). "The giant flightless bird Titanis walleri (Aves: Phorusrhacidae) from the Pleistocene coastal plain of South Texas". Journal of Vertebrate Paleontology. 15 (4): 842–844. Bibcode:1995JVPal..15..842B. doi:10.1080/02724634.1995.10011266.
  9. ^ a b c MacFadden, Bruce J.; Labs-Hochstein, Joann; Hulbert, Richard C.; Baskin, Jon A. (2007). "Revised age of the late Neogene terror bird (Titanis) in North America during the Great American Interchange". Geology. 35 (2): 123–126. Bibcode:2007Geo....35..123M. doi:10.1130/G23186A.1. S2CID 67762754.
  10. ^ Mourer-Chauviré, C.; Tabuce, R.; Mahboubi, M’hammed; Adaci, Mohammed; Bensalah, Mustapha (2011). "A Phororhacoid bird from the Eocene of Africa". Naturwissenschaften. 98 (10): 815–823. Bibcode:2011NW.....98..815M. doi:10.1007/s00114-011-0829-5. PMID 21874523. S2CID 19805809.
  11. ^ a b c Angst, D.; Buffetaut, E.; Lécuyer, C.; Amiot, R. (2013). ""Terror Birds" (Phorusrhacidae) from the Eocene of Europe Imply Trans-Tethys Dispersal". PLOS ONE. 8 (11): e80357. Bibcode:2013PLoSO...880357A. doi:10.1371/journal.pone.0080357. PMC 3842325. PMID 24312212.
  12. ^ a b c Mayr, G. (2017). "Cariamiforms and Diurnal Birds of Prey". Avian Evolution: The Fossil Record of Birds and its Paleobiological Significance. Chichester: Wiley-Blackwell. pp. 189–204. ISBN 978-1119020769.
  13. ^ a b Mayr, G. (2022). "Accipitriformes (New World Vultures, Hawks, and Allies), Falconiformes (Falcons), and Cariamiformes (Seriemas and Allies)". Paleogene Fossil Birds. Fascinating Life Sciences. Springer Cham. pp. 153–176. doi:10.1007/978-3-030-87645-6_8. ISBN 978-3-030-87644-9.
  14. ^ a b c LaBarge, T. W.; Gardner, J. D.; Organ, C. L. (2024). "The evolution and ecology of gigantism in terror birds (Aves, Phorusrhacidae)". Proceedings of the Royal Society B: Biological Sciences. 291 (2021). 20240235. doi:10.1098/rspb.2024.0235. PMC 11040249. PMID 38654650. Supplementary Information
  15. ^ Acosta Hospitaleche, Carolina; Jones, Washington (2024). "Were terror birds the apex continental predators of Antarctica? New findings in the early Eocene of Seymour Island". Palaeontologia Electronica. 27 (1): 1–31. doi:10.26879/1340.
  16. ^ Benton, R. C.; Terry, D. O. Jr.; Evanoff, E.; McDonald, H. G. (25 May 2015). The White River Badlands: Geology and Paleontology. Indiana University Press. p. 95. ISBN 978-0253016089.
  17. ^ a b Cracraft, J. (1968). "A review of the Bathornithidae (Aves, Gruiformes), with remarks on the relationships of the suborder Cariamae". American Museum Novitates (2326): 1–46. hdl:2246/2536.
  18. ^ Agnolin, Federico L. (2009). Sistemática y Filogenia de las Aves Fororracoideas (Gruiformes, Cariamae) [Systematics and Phylogeny of Phororrhacoid Birds (Gruiformes, Cariamae)] (in Spanish). Fundación de Historia Natural Felix de Azara. pp. 1–79.
  19. ^ Mayr, G.; Noriega, J. (2013). "A well-preserved partial skeleton of the poorly known early Miocene seriema Noriegavis santacrucensis (Aves, Cariamidae)". Acta Palaeontologica Polonica. doi:10.4202/app.00011.2013. hdl:11336/41730.
  20. ^ Tambussi, CP; de Mendoza, R; Degrange, FJ; Picasso, MB. (2013). "Flexibility along the Neck of the Neogene Terror Bird Andalgalornis steulleti (Aves Phorusrhacidae)". PLOS ONE. 7 (5): e37701. Bibcode:2012PLoSO...737701T. doi:10.1371/journal.pone.0037701. PMC 3360764. PMID 22662194.
  21. ^ Bertelli, Sara; Chiappe, Luis M; Tambussi, Claudia (2007). "A New Phorusrhacid (Aves: Cariamae) from the Middle Miocene of Patagonia, Argentina". Journal of Vertebrate Paleontology. 27 (2): 409–419. doi:10.1671/0272-4634(2007)27[409:ANPACF]2.0.CO;2. S2CID 85693135.
  22. ^ Antón, Mauricio (2013). Sabertooth. Bloomington, Indiana: University of Indiana Press. p. 61. ISBN 9780253010421.
  23. ^ Jones, Washington W. (2010). Nuevos aportes sobre la paleobiología de los fororrácidos (Aves: Phorusrhacidae) basados en el análisis de estructuras biológicas [New contributions on the paleobiology of phororrhacids (Aves: Phorusrhacidae) based on the analysis of biological structures] (PDF) (PhD thesis) (in Spanish). Uruguay: Universidad de la República - Facultad de Ciencias.
  24. ^ Melchor, R; Feola, S (September 2023). "First terror bird footprints reveal functionally didactyl posture". Nature. 13 (1): 16474. Bibcode:2023NatSR..1316474M. doi:10.1038/s41598-023-43771-x. PMC 10542783. PMID 37777554.
  25. ^ a b c Chiappe, Luis M.Bertelli; Sara (2006). "Palaeontology: Skull Morphology Of Giant Terror Birds". Nature. 443 (7114): 929. Bibcode:2006Natur.443..929C. doi:10.1038/443929a. PMID 17066027. S2CID 4381103.
  26. ^ Degrange, Federico J.; Tambussi, Claudia P. (2011). "Re-examination of Psilopterus lemoinei (Aves, Phorusrhacidae), a late early Miocene little terror bird from Patagonia (Argentina)". Journal of Vertebrate Paleontology. 31 (5): 1080–1092. Bibcode:2011JVPal..31.1080D. doi:10.1080/02724634.2011.595466. S2CID 86790415.
  27. ^ Bakker, Robert; et al. (1998). "Brontosaur Killers: Late Jurassic Allosaurids as Sabre-tooth Cat Analogues" (PDF). GAIA. 15 (8): 145–158.
  28. ^ Nash, Duane (2015-09-02). "Terror Birds Cometh: A New Hypothesis Unlocking Phorusrhacid Feeding Dynamics & Ecology". Antediluvian Salad.
  29. ^ Wroe, Stephen; et al. (2010). "Mechanical Analysis Of Feeding Behavior In The Extinct "Terror Bird' Andalgalornis steulleti (Gruiformes: Phorusrhacidae)". PLOS ONE. 5 (8): 1–7. Bibcode:2010PLoSO...511856D. doi:10.1371/journal.pone.0011856. PMC 2923598. PMID 20805872.
  30. ^ King, Logan; Barrick, Reese (October 2016). Semicircular canal shape within Aves and non-avian Theropoda: Utilizing geometric morphometrics to correlate life history with canal cross-sectional shape. Society of Vertebrate Paleontology 76th Annual Meeting At: Salt Lake City, Utah, United States.
  31. ^ "Ancient "terror bird" used powerful beak to jab like an agile boxer". OHIO: Research. Aug 18, 2010. Archived from the original on 2017-05-16.
  32. ^ Ameghino, Florentino (1936). Torcelli, A.J. (ed.). Obras completas y correspondencia cientifica de Florentino Ameghino. Vol. 21. La Plata: Taller de Impresiones Oficiales. p. 573.
  33. ^ a b Angst, D.; Buffetaut, E. (16 November 2017). Palaeobiology of giant flightless birds. Oxford: Elsevier Science. pp. 157–158. ISBN 978-1785481369. OCLC 1012400051.
  34. ^ Nasif, Norma L.; Esteban, Graciela I.; Ortiz, Pablo E. (2009). "Novedoso hallazgo de egagrópilas en el Mioceno tardío, Formación Andalhuala, provincia de Catamarca, Argentina". Serie Correlación Geológica. 25 (105–114).
  35. ^ Creisler, Ben (2012-06-26). "Phorusrhacos "wrinkle bearer (jaw)": Etymology and Meaning". usc.edu dinosaur (Mailing list). Archived from the original on 2016-03-04.
  36. ^ Ksepka, Daniel (6 February 2017). "Flights of Fancy in Avian Evolution". American Scientist. 102: 36. doi:10.1511/2014.106.36. Retrieved 11 May 2023.
  37. ^ Degrange, Federico J. (2020). "A revision of skull morphology in Phorusrhacidae (Aves, Cariamiformes)". Journal of Vertebrate Paleontology. 40 (6): e1848855. Bibcode:2020JVPal..40E8855D. doi:10.1080/02724634.2020.1848855. S2CID 234119602.
  38. ^ Cracraft, J. (1968). "A review of the Bathornithidae (Aves, Gruiformes), with remarks on the relationships of the suborder Cariamae". American Museum Novitates (2326).
  39. ^ a b Mayr, Gerald (2016). "Osteology and phylogenetic affinities of the middle Eocene North American Bathornis grallator —one of the best represented, albeit least known Paleogene cariamiform birds (seriemas and allies)". Journal of Paleontology. 90 (2): 357–374. Bibcode:2016JPal...90..357M. doi:10.1017/jpa.2016.45. ISSN 0022-3360. S2CID 88936361.
  40. ^ Alvarenga, Herculano M.F.; Höfling, Elizabeth (2003). "Systematic revision of the Phorusrhacidae (Aves: Ralliformes)". Papéis Avulsos de Zoologia. 43 (4): 55–91. doi:10.1590/S0031-10492003000400001.
  41. ^ Cenizo, Marcos M. (2012). "Review Of The Putative Phorusrhacidae From The Cretaceous And Paleogene Of Antarctica: New Records Of Ratites And Pelagornithid Birds" (PDF). Polish Polar Research. 33 (3): 239–258. doi:10.2478/v10183-012-0014-3.
  42. ^ Federico L. Agnolin & Pablo Chafrat (2015). "New fossil bird remains from the Chichinales Formation (Early Miocene) of northern Patagonia, Argentina". Annales de Paléontologie. 101 (2): 87–94. Bibcode:2015AnPal.101...87A. doi:10.1016/j.annpal.2015.02.001.
  43. ^ Alvarenga, HMF; Höfling, E (2003). "Systematic revision of the Phorusrhacidae (Aves: Ralliformes)" (PDF). Papéis Avulsos de Zoologia. 43 (4): 55–91. doi:10.1590/s0031-10492003000400001.
  44. ^ Alvarenga, Herculano (2014). "South American and Antarctic Continental Cenozoic Birds — Paleobiogeographic Affinities and Disparities". Ameghiniana. 51 (3). Asociacion Paleontologica Argentina: 266. doi:10.5710/amgh.v51i3.2. ISSN 0002-7014. S2CID 126914134.
  45. ^ Tambussi, Claudia; Ubilla, Martín; Perea, Daniel (1999). "The youngest large carnassial bird (Phorusrhacidae, Phorusrhacinae) from South America (Pliocene-Early Pleistocene of Uruguay)". Journal of Vertebrate Paleontology. 19 (2): 404–406. Bibcode:1999JVPal..19..404T. doi:10.1080/02724634.1999.10011154. ISSN 0272-4634. JSTOR 4524003.
  46. ^ Chandler, Robert M; Jefferson, George T; Lindsay, Lowell; Vescera, Susan P (2013-04-01). The Terror Bird, Titanis (Phorusrhacidae) from Pliocene Olla Formation, Anza-Borrego Desert State Park, Southern California (PDF). Raising Questions in the central Mojave Desert: The 2013 Desrt Symposium Field Guide and Proceedings. pp. 181–183. Archived from the original (PDF) on 2023-07-21.
  47. ^ a b Federico J. Degrange; Claudia P. Tambussi; Matías L. Taglioretti; Alejandro Dondas; Fernando Scaglia (2015). "A new Mesembriornithinae (Aves, Phorusrhacidae) provides new insights into the phylogeny and sensory capabilities of terror birds". Journal of Vertebrate Paleontology. 35 (2): e912656. Bibcode:2015JVPal..35E2656D. doi:10.1080/02724634.2014.912656. hdl:11336/38650. S2CID 85212917.
  48. ^ Mayr, Gerald (2005-04-15). "Old World phorusrhacids (Aves, Phorusrhacidae): a new look at Strigogyps ("Aenigmavis") sapea (Peters 1987)" (abstract). PaleoBios. 25 (1): 11–16. Retrieved 2008-07-04.
  49. ^ Hackett, Shannon J.; et al. (2008-06-27). "A Phylogenomic Study of Birds Reveals Their Evolutionary History". Science. 320 (5884): 1763–1768. Bibcode:2008Sci...320.1763H. doi:10.1126/science.1157704. PMID 18583609. S2CID 6472805.
  50. ^ Alexander Suh; et al. (2011-08-23). "Mesozoic retroposons reveal parrots as the closest living relatives of passerine birds". Nature Communications. 2 (8): 443. Bibcode:2011NatCo...2..443S. doi:10.1038/ncomms1448. PMC 3265382. PMID 21863010.
  51. ^ 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). "Whole-genome analyses resolve early branches in the tree of life of modern birds" (PDF). Science. 346 (6215): 1320–1331. Bibcode:2014Sci...346.1320J. doi:10.1126/science.1253451. hdl:10072/67425. PMC 4405904. PMID 25504713. Archived from the original (PDF) on 2019-12-06. Retrieved 2018-05-27.
  52. ^ Webb, S. David (23 August 2006). "The Great American Biotic Interchange: Patterns and Processes". Annals of the Missouri Botanical Garden. 93 (2): 245–257. doi:10.3417/0026-6493(2006)93[245:TGABIP]2.0.CO;2. S2CID 198152030.
  53. ^ Marshall, Larry G. (1994). "The Terror Birds of South America" (PDF). Scientific American. 270 (2). Springer Science and Business Media LLC: 90–95. Bibcode:1994SciAm.270b..90M. doi:10.1038/scientificamerican0294-90. ISSN 0036-8733.
  54. ^ Gasparini, Zulma (September 1984). "New Tertiary Sebecosuchia (Crocodylia: Mesosuchia) from Argentina". Journal of Vertebrate Paleontology. 4 (1): 85–95. Bibcode:1984JVPal...4...85G. doi:10.1080/02724634.1984.10011988. JSTOR 4522967.
  55. ^ Naish, Darren (30 May 2001). "Dumb Metatherians vs Evil, Smart Placentals". USC dinosaur (Mailing list). Archived from the original on 2011-11-20.
  56. ^ Kraglievich, J.L.; Olazabal, A.G. (1959-01-01). "Los prociónidos extinguidos del género Chapalmalania Ameghino". Revista del Museo Argentino de Ciencias Naturales (in Spanish). 6. Museo Argentino de Ciencia Naturales: 1–59. ISSN 1514-5158.
  57. ^ Prevosti, Francisco J; Forasiepi, Analía; Zimicz, Natalia (2013). "The Evolution Of The Cenozoic Terrestrial Mammalian Predator Guild In South America: Competition Or Replacement?". Journal of Mammalian Evolution. 20 (1): 3–21. doi:10.1007/s10914-011-9175-9. hdl:11336/2663. S2CID 15751319.
  58. ^ Alvarenga, H.; Jones, W.; Rinderknecht, A. (2010). "The youngest record of phorusrhacid birds (Aves, Phorusrhacidae) from the late Pleistocene of Uruguay" (PDF). Neues Jahrbuch für Geologie und Paläontologie - Abhandlungen. 256 (2): 229–234. doi:10.1127/0077-7749/2010/0052.
  59. ^ Corona, Andrea; Perea, Daniel; Toriño, Pablo; Goso, Cesar (2012). "Taphonomy, sedimentology and chronology of a fossiliferous outcrop from the continental Pleistocene of Uruguay". Revista Mexicana de Ciencias Geológicas. 29 (2): 514–525 – via ResearchGate.
  60. ^ Cid, A.S.; Anjos, R.M.; Zamboni, C.B.; Cardoso, R.; Muniz, M.; Corona, A.; Valladares, D.L.; Kovacs, L.; Macario, K.; Perea, D.; Goso, C.; Velasco, H. (2014). "Na, K, Ca, Mg, and U-series in fossil bone and the proposal of a radial diffusion–adsorption model of uranium uptake". Journal of Environmental Radioactivity. 136: 131–139. Bibcode:2014JEnvR.136..131C. doi:10.1016/j.jenvrad.2014.05.018. hdl:11336/5799. PMID 24953228.
[edit]
Wikimedia Commons has media related to Phorusrhacidae.
Retrieved from "https://en.wikipedia.org/w/index.php?title=Phorusrhacidae&oldid=1253064735"