Biology:Phorusrhacidae

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Short description: Extinct family of flightless birds

Phorusrhacidae
Temporal range: Early Eocene – Late Pleistocene[1]
~53–0.1 Ma
Skeleton of Titanis at the Florida Museum of Natural History.jpg
Reconstructed skeleton of Titanis walleri, Florida Museum of Natural History
Scientific classification e
Domain: Eukaryota
Kingdom: Animalia
Phylum: Chordata
Class: Aves
Order: Cariamiformes
Superfamily: †Phorusrhacoidea
Ameghino, 1889
Family: †Phorusrhacidae
Ameghino, 1889[2]
Type species
†Phorusrhacos longissimus
Ameghino, 1887
Subfamilies
  • †Brontornithinae?
  • †Mesembriornithinae
  • †Patagornithinae
  • †Phorusrhacinae
  • †Psilopterinae
Synonyms

Phorusrhacids, colloquially known as terror birds, are an extinct family of large carnivorous flightless birds that were among the largest apex predators in South America during the Cenozoic era; their conventionally accepted temporal range covers from 53 to 0.1 million years (Ma) ago.[1]

They ranged in height from 1 to 3 m (3 to 10 ft). 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).[3]

It was once believed that T. walleri became extinct in North America around the time of the arrival of humans,[4] but subsequent datings of Titanis fossils provided no evidence for their survival after 1.8 Ma.[5] However, reports from Uruguay of new findings of a relatively small form (Psilopterus) dating to 18,000[6] and 96,000[7] years ago would imply that phorusrhacids survived there until very recently (i.e., until the late Pleistocene); the initial report of such a recent date has been questioned.[8]

Phorusrhacids may have even made their way into Africa; the genus Lavocatavis was discovered in Algeria, but its status as a true phorusrhacid is questioned.[9] A possible European form, Eleutherornis, has also been identified, suggesting that this group had a wider geographical range in the Paleogene.[10][11]

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.[12][13] At least one analysis recovers Bathornis as sister taxa to phorusrhacids, on the basis of shared features in the jaws and coracoid,[14] though this has been seriously contested, as these might have evolved independently for the same carnivorous, flightless lifestyle.[15]

Description

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.[16]

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).[17] 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.[18]

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.[19] 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.[20]

Skull structure

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[21] 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.[21] The structure of the fossils also suggest that these birds may have been swifter than originally thought.[21]

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.[22]

Palaeobiology

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.[23][24] 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,[25] 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.[26]

Diet

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.[27] 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.[28][29] However, Ameghino never formally described these specimens and they have not yet been relocated, making it difficult to determine if they are phorusrhacid pellets.[29] Fossilized pellets from northwestern Argentina have also been suggested to pertain to small phorusrhacids like Procariama.[30]

Classification

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.[31] 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.[32] 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.[33] 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.[34] 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.[35]

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:[35]

 
 

Opisthocomidae

 
 

Paracrax

 
 

Elaphrocnemus

 
 Cariamiformes 
 

Bathornis

 
 

Ameghinornis

 
 

Dynamopterus

 
 
 

Cariama

 
 

Phorusrhacidae

 
 
 
 

Following the revision by Alvarenga and Höfling (2003), there are now 5 subfamilies, containing 14 genera and 18 species:[36] These species were the product of adaptive radiation.[37]

Superfamily Phorusrhacoidea

  • Genus Lavocatavis – Middle Eocene Glib Zegdou Formation of Algeria
Reconstructed skeleton of Paraphysornis at the Museu Nacional, Rio de Janeiro

Family Phorusrhacidae

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.[43] Though traditionally considered as members of the Gruiformes, based on both morphological and genetic studies (the latter being based on the seriemaCite error: Closing </ref> missing for <ref> tag (They had been preceded by procyonids as early as 7.3 million years ago.[3]) The population of phorusrhacids declined thereafter according to older hypotheses, suggesting that competition with newly arrived predators was a major contributor to their extinction.[44] Similar ideas have been considered for sparassodonts and for South America's terrestrial sebecid crocodilians.[45]

However, the role of competitive displacement in South American predator lineages has been questioned by some researchers.[46] 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[47]), 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.[48] 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,[13] before becoming extinct in the Early Miocene, about 20 million years ago. The phorusrhacid Titanis expanded northward into a 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.[5] However, several fossil finds of smaller forms have been described from the late Pleistocene of South America. Psilopterus may have been present until 96,040 ± 6,300 years ago.[7] Another unidentified smaller type has also been dated to the late Pleistocene, perhaps 18,000 years ago.[6] These finds, if accepted, extend the existence of the smaller members of this group of avian predators considerably.

References

  1. ↑ 1.0 1.1 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. 
  2. ↑ Ameghino, F (1889). "Contribuición al conocimiento de los mamíferos fósiles de la República Argentina" (in es). Actas Academia Nacional Ciencias de Córdoba 6: 1–1028. 
  3. ↑ 3.0 3.1 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. PMID 21125025. 
  4. ↑ 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. doi:10.1080/02724634.1995.10011266. Bibcode: 1995JVPal..15..842B. 
  5. ↑ 5.0 5.1 5.2 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. doi:10.1130/G23186A.1. Bibcode: 2007Geo....35..123M. 
  6. ↑ 6.0 6.1 Alvarenga, H.; Jones, W.; Rinderknecht, A. (2010). "The youngest record of phorusrhacid birds (Aves, Phorusrhacidae) from the late Pleistocene of Uruguay". Neues Jahrbuch für Geologie und Paläontologie - Abhandlungen 256 (2): 229–234. doi:10.1127/0077-7749/2010/0052. http://www.museuhistorianatural.com/pesquisa_arquivos/2010/Phorusrh._Pleist.sup.Alvarenga.pdf. 
  7. ↑ 7.0 7.1 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.  Note: their date of 96 thousand years BP is the maximum age, obtained from the bottom of the fossil-containing stratum.
  8. ↑ Agnolin, Federico (2014-06-26). "La posición sistemática de Hermosiornis (Aves, Phororhacoidea) y sus implicancias filogenéticas" (in es). Revista del Museo Argentino de Ciencias Naturales. Nueva serie 15 (1): 39–60. doi:10.22179/revmacn.15.167. ISSN 1853-0400. http://revista.macn.gob.ar/ojs/index.php/RevMus/article/view/167/158. 
  9. ↑ Mourer-Chauviré, C. (2011). "A Phororhacoid bird from the Eocene of Africa". Naturwissenschaften 98 (10): 815–823. doi:10.1007/s00114-011-0829-5. PMID 21874523. Bibcode: 2011NW.....98..815M. 
  10. ↑ Angst, Delphine; Buffetaut, Eric (2012). "A Large Phorusrhacid Bird From the Middle Eocene of France". 8th International Meeting of the Society of Avian Paleontology and Evolution. p. 9. http://www2.nrm.se/ve/birds/sape/SAPE_abstracts_2012.pdf. 
  11. ↑ 11.0 11.1 11.2 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. doi:10.1371/journal.pone.0080357. PMID 24312212. Bibcode: 2013PLoSO...880357A. 
  12. ↑ 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. https://books.google.com/books?id=ZcFtCQAAQBAJ&pg=PA95. 
  13. ↑ 13.0 13.1 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. 
  14. ↑ Agnolin, Federico L. (2009) (in es). Sistemática y Filogenia de las Aves Fororracoideas (Gruiformes, Cariamae). Fundación de Historia Natural Felix de Azara. pp. 1–79. 
  15. ↑ 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. 
  16. ↑ 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. doi:10.1371/journal.pone.0037701. PMID 22662194. Bibcode: 2012PLoSO...737701T. 
  17. ↑ 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:ANPACF2.0.CO;2]. 
  18. ↑ Antón, Mauricio (2013). Sabertooth. Bloomington, Indiana: University of Indiana Press. p. 61. ISBN 9780253010421. 
  19. ↑ 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 español). Uruguay: Universidad de la República - Facultad de Ciencias.
  20. ↑ Melchor, R; Feola, S (September 2023). "First terror bird footprints reveal functionally didactyl posture". Nature 13 (1): 16474. doi:10.1038/s41598-023-43771-x. PMID 37777554. Bibcode: 2023NatSR..1316474M. 
  21. ↑ 21.0 21.1 21.2 Chiappe, Luis M.Bertelli; Sara (2006). "Palaeontology: Skull Morphology Of Giant Terror Birds". Nature 443 (7114): 929. doi:10.1038/443929a. PMID 17066027. Bibcode: 2006Natur.443..929C. 
  22. ↑ 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. doi:10.1080/02724634.2011.595466. Bibcode: 2011JVPal..31.1080D. 
  23. ↑ Bakker, Robert (1998). "Brontosaur Killers: Late Jurassic Allosaurids as Sabre-tooth Cat Analogues". GAIA 15 (8): 145–158. https://www.researchgate.net/publication/40662858. 
  24. ↑ Nash, Duane (2015-09-02). "Terror Birds Cometh: A New Hypothesis Unlocking Phorusrhacid Feeding Dynamics & Ecology". http://antediluviansalad.blogspot.com/2015/09/terror-birds-cometh-new-theory.html. 
  25. ↑ Wroe, Stephen (2010). "Mechanical Analysis Of Feeding Behavior In The Extinct "Terror Bird' Andalgalornis steulleti (Gruiformes: Phorusrhacidae)". PLOS ONE 5 (8): 1–7. doi:10.1371/journal.pone.0011856. PMID 20805872. Bibcode: 2010PLoSO...511856D. 
  26. ↑ 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. 
  27. ↑ "Ancient "terror bird" used powerful beak to jab like an agile boxer". Aug 18, 2010. https://www.ohio.edu/research/communications/terrorbirds.cfm. 
  28. ↑ Ameghino, Florentino (1936). Obras completas y correspondencia cientifica de Florentino Ameghino. 21. La Plata: Taller de Impresiones Oficiales. p. 573. 
  29. ↑ 29.0 29.1 Angst, D.; Buffetaut, E. (16 November 2017). Palaeobiology of giant flightless birds. Oxford: Elsevier Science. pp. 157–158. ISBN 978-1785481369. OCLC 1012400051. https://books.google.com/books?id=aU4ADQAAQBAJ&q=fossilized%20pellets. 
  30. ↑ 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). 
  31. ↑ 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.
  32. ↑ Ksepka, Daniel (6 February 2017). "Flights of Fancy in Avian Evolution" (in en). American Scientist 102: 36. doi:10.1511/2014.106.36. https://www.americanscientist.org/article/flights-of-fancy-in-avian-evolution. Retrieved 11 May 2023. 
  33. ↑ Degrange, Federico J. (2020). "A revision of skull morphology in Phorusrhacidae (Aves, Cariamiformes)". Journal of Vertebrate Paleontology 40 (6): e1848855. doi:10.1080/02724634.2020.1848855. Bibcode: 2020JVPal..40E8855D. https://www.researchgate.net/publication/348614159. 
  34. ↑ Cracraft, J. (1968). "A review of the Bathornithidae (Aves, Gruiformes), with remarks on the relationships of the suborder Cariamae". American Museum Novitates (2326). https://archive.org/details/reviewbathornit2326crac/reviewbathornit2326crac/. 
  35. ↑ 35.0 35.1 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)" (in en). Journal of Paleontology 90 (2): 357–374. doi:10.1017/jpa.2016.45. ISSN 0022-3360. Bibcode: 2016JPal...90..357M. https://www.cambridge.org/core/product/identifier/S0022336016000457/type/journal_article. 
  36. ↑ 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. 
  37. ↑ Cenizo, Marcos M. (2012). "Review Of The Putative Phorusrhacidae From The Cretaceous And Paleogene Of Antarctica: New Records Of Ratites And Pelagornithid Birds". Polish Polar Research 33 (3): 239–258. doi:10.2478/v10183-012-0014-3. https://www.degruyter.com/downloadpdf/j/popore.2012.33.issue-3/v10183-012-0014-3/v10183-012-0014-3.pdf. 
  38. ↑ 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. doi:10.1016/j.annpal.2015.02.001. Bibcode: 2015AnPal.101...87A. 
  39. ↑ Alvarenga, Herculano (2014). "South American and Antarctic Continental Cenozoic Birds — Paleobiogeographic Affinities and Disparities". Ameghiniana (Asociacion Paleontologica Argentina) 51 (3): 266. doi:10.5710/amgh.v51i3.2. ISSN 0002-7014. 
  40. ↑ 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". Raising Questions in the central Mojave Desert: The 2013 Desrt Symposium Field Guide and Proceedings. pp. 181–183. http://www.desertsymposium.org/DS_2013_Raising_Questions.pdf. 
  41. ↑ Alvarenga, HMF; Höfling, E (2003). "Systematic revision of the Phorusrhacidae (Aves: Ralliformes)". Papéis Avulsos de Zoologia 43 (4): 55–91. doi:10.1590/s0031-10492003000400001. http://www.scielo.br/pdf/paz/v43n4/17491.pdf. 
  42. ↑ 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. doi:10.1080/02724634.2014.912656. Bibcode: 2015JVPal..35E2656D. 
  43. ↑ 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. http://www.ucmp.berkeley.edu/science/paleobios/abstracts_21to25.php. Retrieved 2008-07-04. 
  44. ↑ Marshall, Larry G. (1994). "The Terror Birds of South America". Scientific American (Springer Science and Business Media LLC) 270 (2): 90–95. doi:10.1038/scientificamerican0294-90. ISSN 0036-8733. Bibcode: 1994SciAm.270b..90M. http://usuarios.geofisica.unam.mx/cecilia/cursos/TerrorBirds-Marshall94.pdf. 
  45. ↑ Gasparini, Zulma (September 1984). "New Tertiary Sebecosuchia (Crocodylia: Mesosuchia) from Argentina". Journal of Vertebrate Paleontology 4 (1): 85–95. doi:10.1080/02724634.1984.10011988. Bibcode: 1984JVPal...4...85G. 
  46. ↑ Naish, Darren (30 May 2001). "Dumb Metatherians vs Evil, Smart Placentals". USC dinosaur (Mailing list). Archived from the original on 2011-11-20.
  47. ↑ Kraglievich, J.L.; Olazabal, A.G. (1959-01-01). "Los prociónidos extinguidos del género Chapalmalania Ameghino" (in es). Revista del Museo Argentino de Ciencias Naturales (Museo Argentino de Ciencia Naturales) 6: 1–59. ISSN 1514-5158. https://www.researchgate.net/publication/284098225. 
  48. ↑ 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. 

External links

Wikidata ☰ Q752173 entry



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