Pelagornis | |
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Reconstruction of a P. miocaenus skeleton at the NMNH. | |
Scientific classification | |
Domain: | Eukaryota |
Kingdom: | Animalia |
Phylum: | Chordata |
Class: | Aves |
Order: | † Odontopterygiformes |
Family: | † Pelagornithidae |
Genus: | † Pelagornis Lartet, 1857 |
Type species | |
†Pelagornis miocaenus Lartet, 1857 | |
Species | |
†P. miocaenusLartet, 1857 Contents | |
Synonyms | |
see text |
Pelagornis is an extinct genus of prehistoric pseudotooth birds, a group of extinct seabirds. Species span from the Oligocene to the Early Pleistocene. Members of Pelagorinis represent among the largest pseudotooth birds, with one species. P. sandersi, having the widest wingspan of any bird known.
Four species have been formally described, but several other named taxa of pseudotooth birds might belong in Pelagornis too. The type species Pelagornis miocaenus is known from Aquitanian (Early Miocene) sediments – formerly believed to be of Middle Miocene age – of Armagnac (France). The original specimen on which P. miocaenus was founded was a left humerus almost the size of a human arm. The scientific name – "the most unimaginative name ever applied to a fossil" in the view of Storrs L. Olson [1] – does in no way refer to the bird's startling and at that time unprecedented proportions, and merely means "Miocene pelagic bird". Like many pseudotooth birds, it was initially believed to be related to the albatrosses in the tube-nosed seabirds (Procellariiformes), but subsequently placed in the Pelecaniformes where it was either placed in the cormorant and gannet suborder (Sulae) or united with other pseudotooth birds in a suborder Odontopterygia. [2]
While P. miocaenus was the first pseudotooth bird species to be described scientifically, its congener Pelagornis mauretanicus was only named in 2008. It was a slightly distinct and markedly younger species. Its remains have been found in 2.5 Ma Gelasian (Late Pliocene/Early Pleistocene, MN17) deposits at Ahl al Oughlam (Morocco). [3]
Additional fossils are placed in Pelagornis, usually without assignment to species, mainly due to their large size and Miocene age. From the United States, such specimens have been found in the Middle Miocene Calvert Formation of Maryland and Virginia, and the contemporary Pungo River Formation of the Lee Creek Mine in North Carolina (though at least one other pelagornithid is probably represented among this material too). USNM 244174 (a tarsometatarsus fragment) was found near Charleston, South Carolina and assigned to P. miocaenus, and the slightly smaller left tarsometatarsal middle trochlea USNM 476044 might also belong here. A broken but fairly complete sternum probably of this genus, specimen LHNB (CCCP)-1, is known from the Serravallian-Tortonian boundary (Middle to Late Miocene) near Costa da Caparica in Portugal. Contemporary are certain specimens [4] from the Bahía Inglesa Formation of Chile, while other material from this formation [5] as well as remains from the Pisco Formation of Peru are from the Late Miocene to Early Pliocene. [6]
It is not clear whether the South American fossils – of similar size and age and not including directly comparable bones – are from one or two species. A very worn sternum and some other remains from the Miocene of Oregon as well as roughly contemporary material from California are sometimes assigned to Pelagornis, but this appears to be an error; if not of the contemporary North Pacific Osteodontornis , the specimen is better regarded as indeterminable. Given the distance in space and time involved, all Pacific material may well have been a species different from P. miocaenus or even from birds closer to Osteodontornis. Indeed, some of the older Bahía Inglesa Formation remains [7] tentatively referred to Pelagornis were at first assigned to the mysterious Pseudodontornis longirostris in error, and a proximal (initially misidentified as distal) humerus piece (CMNZ AV 24,960), from the Waiauan (Middle-Late Miocene) cliffs near the mouth of the Waipara River (North Canterbury, New Zealand) seems to differ little from either O. orri or P. miocaenus. The Pisco Formation specimens – which may be from the same species as the Bahía Inglesa ones, or from its direct descendant – on the other hand seem to be well distinct from Osteodontornis. It must be remembered, however, that the Isthmus of Panama had not been formed yet during the Miocene. [8]
Pelagornis sandersi was described in July 2014, whose fossil remains date from 25 million years ago, during the Chattian age of the Oligocene. [9] [10] The only known fossil of P. sandersi was first uncovered in 1983 at Charleston International Airport, South Carolina, discovered by James Malcom, while working construction building a new terminal there. At the time the bird lived, 25 million years ago, global temperatures were higher, and the area where it was discovered was an ocean. [11] [12] After excavation, the fossil of P. sandersi was catalogued and put in storage at the Charleston Museum, where it remained until it was rediscovered by paleontologist Dan Ksepka in 2010. [13] [14] The bird is named after Albert Sanders, the former curator of natural history at the Charleston Museum, who led the excavation of P. sandersi. [15] It currently sits at the Charleston Museum, where it was identified as a new species by Ksepka in 2014. [10]
A humerus from the Muséum d'Histoire naturelle de Bordeaux was labelled "Pelagornis Delfortrii 1869". Though the name from the label had been listed in the synonymy of P. miocaenus, neither does it seem to be a validly established taxon nor was the specimen compared with P. miocaenus remains. It seems to refer to one of the syntypes of the procellariiform Plotornis delfortrii – found at Léognan (France) and also of Aquitanian age – from which that species was described in the 1870s by Alphonse Milne-Edwards: when the nomen nudum "Pelagornis delfortrii" is listed in the synonymy of P. miocaenus, the pseudotooth bird is claimed to be known from the Léognan deposits also, whereas it has not actually been found there. Pseudodontornis , meanwhile, is a generally Paleogene genus of huge pseudotooth birds. All its species are not uncommonly considered synonymous with earlier-described taxa. The (probably) Eo-Oligocene type species Pseudodontornis longirostris might belong in Pelagornis, though given its uncertain age and provenance a comparison with undisputed Pelagornis material – which is currently lacking – would seem to be necessary before such a step is taken. In that respect, Palaeochenoides mioceanus was also hypothesized to include P. longirostris, and would need to be compared with Pelagornis to see whether it does not belong here too. [16]
There has been little dedicated study of the relationships of Pelagornis, for while quite a lot of remains are known from the present genus, those of most other pseudotooth birds are few and far between and direct comparisons are further hampered by the damaged state of most remains. The large Gigantornis eaglesomei from the Middle Eocene Atlantic was established based on a broken but not too incomplete sternum and might actually belong in Dasornis . In Gigantornis the articular facet for the furcula consists of a flat section at the very tip of the sternal keel and a similar one set immediately above it at an outward angle, and the spina externa is shaped like an Old French shield in cross-section. The slightly smaller LHNB (CCCP)-1 has a less sharply protruding sternal keel, the articular facet for the furcula consists of a large knob at the forward margin, and the spina externa is narrow in cross-section. While these differences are quite conspicuous, the two fossils are clearly of closely related huge dynamically soaring seabirds, and considering the 30 million years or so that separate Gigantornis and LHNB (CCCP)-1, the Paleogene taxon may be very close to the Miocene bird's ancestor nonwithstanding their differences. [17]
In any case, the family name of the pseudotooth birds, Pelagornithidae, as the senior synonym has widely replaced the once-commonly used Pseudodontornithidae. It may be that Pseudodontornis belongs to a distinct lineage of these birds, and then the family name would perhaps be revalidated. Also, the presumed similarity between Dasornis [18] and the smaller Odontopteryx seems to be a symplesiomorphy that is not informative regarding their relationships to each other and with Pelagornis. Rather, it is likely that the huge pseudotooth birds form a clade, and in this case, Pseudodontornithidae like Cyphornithidae and Dasornithidae is correctly placed in the synonymy of Pelagornithidae even if several families were accepted in the Odontopterygiformes. [19]
The sole specimen of P. sandersi has a wingspan estimated between approximately 6.06 and 7.38 m (19.9 and 24.2 ft), [9] giving it the largest wingspan of any flying bird yet discovered, twice that of the wandering albatross, which has the largest wingspan of any extant bird (up to 3.7 m (12 ft)). [20] In this regard, it supplants the previous record holder, the also extinct Argentavis magnificens . The skeletal wingspan (excluding feathers) of P. sandersi is estimated at 5.2 m (17 ft) while that of A. magnificens is estimated at 4 m (13 ft). [15] [21]
The fossil specimens show that P. miocaenus was one of the largest pseudotooth birds, hardly smaller in size than Osteodontornis or the older Dasornis . Its head must have been about 40 cm (16 in) long in life, and its wingspan was probably more than 5 m (16 ft), perhaps closer to 6 metres (20 ft).
Like all members of the Pelagornithidae, P. sandersi had tooth-like or knob-like extensions of the bill's margin, called "pseudo-teeth," which would have enabled the living animal to better grip and grasp slippery prey. According to Ksepka, P. sandersi's teeth "don’t have enamel, they don’t grow in sockets, and they aren’t lost and replaced throughout the creature’s life span." [11] Unlike in its contemporary Osteodontornis but like in the older Pseudodontornis , between each two of Pelagornis's large "teeth" was a single smaller one. The salt glands inside the eye sockets were extremely large and well-developed in Pelagornis.
Pelagornis differed from Dasornis and its smaller contemporary Odontopteryx in having no pneumatic foramen in the fossa pneumotricipitalis of the humerus, a single long latissimus dorsi muscle attachment site on the humerus instead of two distinct segments, and no prominent ligamentum collaterale ventrale attachment knob on the ulna. Further differences between Odontopteryx and Pelagornis are found in the tarsometatarsus: in the latter, it has a deep fossa of the hallux' first metatarsal bone, whereas its middle-toe trochlea is not conspicuously expanded forward. From the humerus pieces of specimen LACM 127875, found in the Eo-Oligocene Pittsburg Bluff Formation near Mist, Oregon (United States), P. miocaenus differs in an external tuberosity that is not as much extended towards shoulder and that is separated from the elbow end by a wider depression. The head of the humerus is turned more to the inward side and the large protuberance found there is not as far towards the end. The Waipara River humerus mentioned above agrees with P. miocaenus in that respect. If the Oregon fossils are related to Cyphornis and/or Osteodontornis, and if the traits as found in P. miocaenus and the New Zealand specimen are apomorphic, the latter two may indeed be very close relatives. [22]
P. sandersi had short, stumpy legs, and was probably only able to fly by hopping off cliff edges. [21] This is supported by its location being near coasts. Originally, there were controversies over whether or not P. sandersi would be able to fly. Previously, the assumed maximum wingspan of a flying bird was 17 ft (5.2 m), because it was hypothesized that above 17 ft, the power required to keep the bird in flight would surpass the power capacity of the bird's muscles. However, this calculation is based on the assumption that the bird in question stays aloft by repeatedly flapping its wings, whereas P. sandersi more likely glided on ocean air currents close to the water, which is less power-intensive than reaching high altitudes. [14] [23] It has been estimated that it was able to fly at up to 60 km/h (37 mph). [21] P. sandersi's long wingspan and gliding power would have enabled it to travel long distances without landing while hunting. [12] Due to P. sandersi's size, the bird likely molted all of its flight feathers at once, similarly to a grebe, since larger feathers take longer to regrow. [12] P. sandersi is theorized to have glided and traveled similarly to a modern albatross, however, according to Dan Ksepka, its closest modern relatives are chickens and ducks. [13]
Some scientists expressed surprise at the idea that this species could fly at all, given that, at between 22 and 40 kg (48 and 88 lb), it would be considered too heavy by the predominant theory of the mechanism by which birds fly. [24] Dan Ksepka of the National Evolutionary Synthesis Center in Durham, North Carolina, who identified that the discovered fossils belonged to a new species, thinks it was able to fly in part because of its relatively small body and long wings, [25] and because it, like the albatross, spent much of its time over the ocean. [11] Ksepka is currently focused on solving how P. sandersi evolved and what caused the species to go extinct. [13]
Fossils of Pelagornis have been found in: [26]
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The bird family Sulidae comprises the gannets and boobies. Collectively called sulids, they are medium-large coastal seabirds that plunge-dive for fish and similar prey. The 10 species in this family are often considered congeneric in older sources, placing all in the genus Sula. However, Sula and Morus (gannets) can be readily distinguished by morphological, behavioral, and DNA sequence characters. Abbott's booby (Papasula) is given its own genus, as it stands apart from both in these respects. It appears to be a distinct and ancient lineage, maybe closer to the gannets than to the true boobies.
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Argentavis is an extinct genus of teratornithid known from three sites in the Epecuén and Andalhualá Formations in central and northwestern Argentina dating to the Late Miocene (Huayquerian). The type species, A. magnificens, is sometimes called the giant teratorn. Argentavis was among the largest flying birds to ever exist, holding the record for heaviest flying bird, although it was surpassed in wingspan after the 2014 description of Pelagornis sandersi, which is estimated to have possessed wings some 20% longer than those of Argentavis.
Teratornithidae is an extinct family of very large birds of prey that lived in North and South America from the Late Oligocene to Late Pleistocene. They include some of the largest known flying birds. Its members are known as teratorns.
Limnofregata is an extinct genus of primitive frigatebird. The two known species were described after fossils from the Early Eocene Green River Formation of Wyoming. A number of good complete and partial skeletons, some with feather impressions, are known of the type species, Limnofregata azygosternon, and L. hasegawai is known from two skulls and most of one torso.
Osteodontornis is an extinct seabird genus. It contains a single named species, Osteodontornis orri, which was described quite exactly one century after the first species of the Pelagornithidae was. O. orri was named after Santa Barbara Museum of Natural History paleontologist Phil C. Orr, for his recognition of the importance of the specimen.
The Pelagornithidae, commonly called pelagornithids, pseudodontorns, bony-toothed birds, false-toothed birds or pseudotooth birds, are a prehistoric family of large seabirds. Their fossil remains have been found all over the world in rocks dating between the Early Paleocene and the Pliocene-Pleistocene boundary.
"Precursor" is a controversial prehistoric bird genus from the Early Eocene. It was established based on fossils found in England, including in the famous London Clay deposits. Three species are included in the genus: "P." parvus, the type species, "P." magnus, and "P." litorum, all named by Colin Harrison and Cyril Walker in 1977.
Copepteryx is an extinct genus of flightless bird of the family Plotopteridae, endemic to Japan during the Oligocene living from 28.4 to 23 mya, meaning it existed for approximately 5.4 million years.
Odontopteryx is a genus of the extinct pseudotooth birds or pelagornithids. These were probably rather close relatives of either pelicans and storks, or of waterfowl, and are here placed in the order Odontopterygiformes to account for this uncertainty.
Cyphornis is a genus of the prehistoric pseudotooth birds. These were probably rather close relatives of either pelicans and storks, or of waterfowl, and are here placed in the order Odontopterygiformes to account for this uncertainty.
Dasornis is a genus of prehistoric pseudotooth birds. These were probably close relatives of either pelicans and storks or waterfowl; they are placed in the order Odontopterygiformes to account for this uncertainty.
Gigantornis eaglesomei is a very large prehistoric bird described from a fragmentary specimen from the Eocene of Nigeria. It was originally described as a representative of the albatross family, Diomedeidae, but was later referred to the pseudotooth or bony-toothed bird family, Pelagornithidae. Gigantornis is one of the largest pseudotooth birds, with an inferred wingspan of about 6 m (20 ft) it is among the largest birds ever.
Palaeochenoides is a genus of the prehistoric pseudotooth birds of somewhat doubtful validity. These were probably rather close relatives of either pelicans and storks, or of waterfowl, and are here placed in the order Odontopterygiformes to account for this uncertainty.
Pseudodontornis is a rather disputed genus of the prehistoric pseudotooth birds. The pseudotooth birds or pelagornithids were probably rather close relatives of either pelicans and storks, or of waterfowl, and are here placed in the order Odontopterygiformes to account for this uncertainty. Up to five species are commonly recognized in this genus.
Tympanonesiotes is a somewhat doubtfully valid genus of the prehistoric pseudotooth birds. These were probably rather close relatives of either pelicans and storks, or of waterfowl, and are here placed in the order Odontopterygiformes to account for this uncertainty.
Macrodontopteryx is a genus of the prehistoric pseudotooth birds of somewhat doubtful validity. These animals were probably rather close relatives of either pelicans and storks, or of waterfowl, and are here placed in the order Odontopterygiformes to account for this uncertainty.
Xenerodiops is a genus of extinct birds, containing one species, Xenerodiops mycter. Its fossil remains were found in Egypt by Elwyn L. Simons and first formally described in 1987. It lived in the Oligocene. It has been placed in its own family, Xenerodiopidae; the alternative view is that this family is synonymous with Ardeidae, the herons.