The origin of birds is a contentious and central topic within evolutionary biology. A close relationship between birds and dinosaurs was first proposed in the nineteenth century after the discovery of the primitive bird Archaeopteryx in Germany. Most researchers now support the view that birds are a group of theropod dinosaurs that evolved during the Mesozoic Era.
Birds share a myriad of unique skeletal features with dinosaurs.[1] Moreover, fossils of more than twenty species of dinosaur have been collected which preserve feathers. There are even very small dinosaurs, such as Microraptor and Anchiornis, which have long, vaned, arm and leg feathers forming wings. The Jurassic basal avialan Pedopenna also shows these long foot feathers. Witmer (2009) has concluded that this evidence is sufficient to demonstrate that avian evolution went through a four-winged stage.[2]
Fossil evidence also demonstrates that birds and dinosaurs shared features such as hollow, pneumatized bones, gastroliths in the digestive system, nest-building and brooding behaviors. The ground-breaking discovery of fossilized Tyrannosaurus rex soft tissue allowed a molecular comparison of cellular anatomy and protein sequencing of collagen tissue, both of which demonstrated that T. rex and birds are more closely related to each other than either is to Alligator.[3] A second molecular study robustly supported the relationship of birds to dinosaurs, though it did not place birds within Theropoda, as expected. This study utilized eight additional collagen sequences extracted from a femur of Brachylophosaurus canadensis, a hadrosaur.[4]
Only a few scientists still debate the dinosaurian origin of birds, suggesting descent from other types of archosaurian reptiles. Among the consensus that supports dinosaurian ancestry, the exact sequence of evolutionary events that gave rise to the early birds within maniraptoran theropods is a hot topic. The origin of bird flight is a separate but related question for which there are also several proposed answers.
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Scientific investigation into the origin of birds began shortly after the 1859 publication of Charles Darwin's On the Origin of Species, the ground-breaking book which described his theory of evolution by natural selection.[5] In 1860, a fossilized feather was discovered in Germany's Late Jurassic solnhofen limestone. Christian Erich Hermann von Meyer described this feather as Archaeopteryx lithographica the next year,[6] and Richard Owen described a nearly complete skeleton in 1863, recognizing it as a bird despite many features reminiscent of reptiles, including clawed forelimbs and a long, bony tail.[7]
Biologist Thomas Henry Huxley, known as "Darwin's Bulldog" for his ferocious support of the new theory of evolution, almost immediately seized upon Archaeopteryx as a transitional fossil between birds and reptiles. Starting in 1868, Huxley made detailed comparisons of Archaeopteryx with various prehistoric reptiles and found that it was most similar to dinosaurs like Hypsilophodon and Compsognathus.[8][9] The discovery in the late 1870s of the iconic "Berlin specimen" of Archaeopteryx, complete with a set of reptilian teeth, provided further evidence. Huxley was the first to propose an evolutionary relationship between birds and dinosaurs, although he was opposed by the very influential Owen. Huxley's conclusions were accepted by many biologists, including Baron Franz Nopcsa,[10] while others, notably Harry Seeley,[11] argued that the similarities were due to convergent evolution.
A turning point came in the early twentieth century with the writings of Gerhard Heilmann of Denmark. An artist by trade, Heilmann had a scholarly interest in birds and from 1913 to 1916 published the results of his research in several parts, dealing with the anatomy, embryology, behavior, paleontology, and evolution of birds.[12] His work, originally written in Danish as Vor Nuvaerende Viden om Fuglenes Afstamning, was compiled, translated into English, and published in 1926 as The Origin of Birds.
Like Huxley, Heilmann compared Archaeopteryx and other birds to an exhaustive list of prehistoric reptiles, and also came to the conclusion that theropod dinosaurs like Compsognathus were the most similar. However, Heilmann noted that birds possessed clavicles (collar bones) fused to form a bone called the furcula ("wishbone"), and while clavicles were known in more primitive reptiles, they had not yet been recognized in dinosaurs. Since he was a firm believer in Dollo's law, which states that evolution is not reversible, Heilmann could not accept that clavicles were lost in dinosaurs and re-evolved in birds. He was therefore forced to rule out dinosaurs as bird ancestors and ascribe all of their similarities to convergent evolution. Heilmann stated that bird ancestors would instead be found among the more primitive "thecodont" grade of reptiles.[13] Heilmann's extremely thorough approach ensured that his book became a classic in the field, and its conclusions on bird origins, as with most other topics, were accepted by nearly all evolutionary biologists for the next four decades.[14]
Clavicles are relatively delicate bones and therefore in danger of being destroyed or at least damaged beyond recognition. Nevertheless clavicles had been found in theropod dinosaurs before Heilman wrote his book, but had gone unrecognized.[15] The absence of clavicles in dinosaurs became the orthodox view despite the discovery of clavicles in the primitive theropod Segisaurus in 1936.[16] The next report of clavicles in a dinosaur was in 1983, and that was in a Russian article published before the end of the Cold War.[17]
Contrary to what Heilman believed, paleontologists now accept that clavicles and in most cases furculae are a standard feature not just of theropods but of saurischian dinosaurs. Up to late 2007 ossified furculae (i.e. made of bone rather than cartilage) have been found in nearly all types of theropods except the most basal ones, Eoraptor and Herrerasaurus.[18] The original report of a furcula in the primitive theropod Segisaurus (1936) has been confirmed by a re-examination in 2005.[19] Joined, furcula-like clavicles have also been found in Massospondylus, an Early Jurassic sauropodomorph.[20]
The tide began to turn against the 'thecodont' hypothesis after the 1964 discovery of a new theropod dinosaur in Montana. In 1969, this dinosaur was described and named Deinonychus by John Ostrom of Yale University.[21] The next year, Ostrom redescribed a specimen of Pterodactylus in the Dutch Teyler Museum as another skeleton of Archaeopteryx.[22] The specimen consisted mainly of a single wing and its description made Ostrom aware of the similarities between the wrists of Archaeopteryx and Deinonychus.[23]
In 1972, British paleontologist Alick Walker hypothesized that birds arose not from 'thecodonts' but from crocodile ancestors like Sphenosuchus.[24] Ostrom's work with both theropods and early birds led him to respond with a series of publications in the mid-1970s in which he laid out the many similarities between birds and theropod dinosaurs, resurrecting the ideas first put forth by Huxley over a century before.[25][26][27] Ostrom's recognition of the dinosaurian ancestry of birds, along with other new ideas about dinosaur metabolism,[28] activity levels, and parental care,[29] began what is known as the Dinosaur renaissance, which began in the 1970s and continues to this day.
Ostrom's revelations also coincided with the increasing adoption of phylogenetic systematics (cladistics), which began in the 1960s with the work of Willi Hennig.[30] Cladistics is a method of arranging species based strictly on their evolutionary relationships, using a statistical analysis of their anatomical characteristics. In the 1980s, cladistic methodology was applied to dinosaur phylogeny for the first time by Jacques Gauthier and others, showing unequivocally that birds were a derived group of theropod dinosaurs.[31] Early analyses suggested that dromaeosaurid theropods like Deinonychus were particularly closely related to birds, a result which has been corroborated many times since.[32][33]
The early 1990s saw the discovery of spectacularly preserved bird fossils in several Early Cretaceous geological formations in the northeastern Chinese province of Liaoning.[34][35] In 1996, Chinese paleontologists described Sinosauropteryx as a new genus of bird from the Yixian Formation,[36] but this animal was quickly recognized as a theropod dinosaur closely related to Compsognathus. Surprisingly, its body was covered by long filamentous structures. These were dubbed 'protofeathers' and considered to be homologous with the more advanced feathers of birds,[37] although some scientists disagree with this assessment.[38] Chinese and North American scientists described Caudipteryx and Protarchaeopteryx soon after. Based on skeletal features, these animals were non-avian dinosaurs, but their remains bore fully formed feathers closely resembling those of birds.[39] "Archaeoraptor", described without peer review in a 1999 issue of National Geographic,[40] turned out to be a smuggled forgery,[41] but legitimate remains continue to pour out of the Yixian, both legally and illegally. Feathers or "protofeathers" have been found on a wide variety of theropods in the Yixian,[42][43] and the discoveries of extremely bird-like dinosaurs,[44] as well as dinosaur-like primitive birds,[45] have almost entirely closed the morphological gap between theropods and birds.
A small minority, including ornithologists Alan Feduccia and Larry Martin, continues to assert that birds are instead the descendants of earlier archosaurs, such as Longisquama or Euparkeria.[46][47] Embryological studies of bird developmental biology have raised questions about digit homology in bird and dinosaur forelimbs.[48] However, due to the cogent evidence provided by comparative anatomy and phylogenetics, as well as the dramatic feathered dinosaur fossils from China, the idea that birds are derived dinosaurs, first championed by Huxley and later by Nopcsa and Ostrom, enjoys near-unanimous support among today's paleontologists.[14]
A new theory of bird origins suggests that selection for the expansion of skeletal muscle, rather than the evolution of flight, was the driving force for the emergence of this clade.[49] Muscles became larger in prospectively endothermic saurians, according to this hypothesis, as a response to the loss of the vertebrate mitochondrial uncoupling protein UCP1.[50] In mammals, UCP1 functions within brown adipose tissue to protect newborns against hypothermia. In modern birds and their ancestors, skeletal muscle serves a similar function. In this view, bipedality and other avian skeletal alterations were side effects of muscle hyperplasia, with further evolutionary modifications of the forelimbs, including adaptations for flight or swimming, and vestigiality, being secondary consequences of two-leggedness.
Archaeopteryx has historically been considered the first bird, or Urvogel. Although newer fossil discoveries eliminated the gap between theropods and Archaeopteryx, as well as the gap between Archaeopteryx and modern birds, phylogenetic taxonomists, in keeping with tradition, almost always use Archaeopteryx as a specifier to help define Aves.[51][52] Aves has more rarely been defined as a crown group consisting only of modern birds.[31] Nearly all palaeontologists regard birds as coelurosaurian theropod dinosaurs.[14] Within Coelurosauria, multiple cladistic analyses have found support for a clade named Maniraptora, consisting of therizinosauroids, oviraptorosaurs, troodontids, dromaeosaurids, and birds.[32][33][53] Of these, dromaeosaurids and troodontids are usually united in the clade Deinonychosauria, which is a sister group to birds (together forming the node-clade Eumaniraptora) within the stem-clade Paraves.[32][54]
Other studies have proposed alternative phylogenies in which certain groups of dinosaurs that are usually considered non-avian are suggested to have evolved from avian ancestors. For example, a 2002 analysis found oviraptorosaurs to be basal avians.[55] Alvarezsaurids, known from Asia and the Americas, have been variously classified as basal maniraptorans,[32][33][56][57] paravians,[53] the sister taxon of ornithomimosaurs,[58] as well as specialized early birds.[59][60] The genus Rahonavis, originally described as an early bird,[61] has been identified as a non-avian dromaeosaurid in several studies.[54][62] Dromaeosaurids and troodontids themselves have also been suggested to lie within Aves rather than just outside it.[63][64]
Many distinct anatomical[65] features are shared by birds and theropod dinosaurs. Some of the more interesting similarities are discussed here:
Archaeopteryx, the first good example of a "feathered dinosaur", was discovered in 1861. The initial specimen was found in the solnhofen limestone in southern Germany, which is a lagerstätte, a rare and remarkable geological formation known for its superbly detailed fossils. Archaeopteryx is a transitional fossil, with features clearly intermediate between those of modern reptiles and birds. Discovered just two years after Darwin's seminal Origin of Species, its discovery spurred the nascent debate between proponents of evolutionary biology and creationism. This early bird is so dinosaur-like that, without a clear impression of feathers in the surrounding rock, at least one specimen was mistaken for Compsognathus.[66]
Since the 1990s, a number of additional feathered dinosaurs have been found, providing even stronger evidence of the close relationship between dinosaurs and modern birds. Most of these specimens were unearthed in Liaoning province, northeastern China, which was part of an island continent during the Cretaceous period. Though feathers have been found only in the lagerstätte of the Yixian Formation and a few other places, it is possible that non-avian dinosaurs elsewhere in the world were also feathered. The lack of widespread fossil evidence for feathered non-avian dinosaurs may be because delicate features like skin and feathers are not often preserved by fossilization and thus are absent from the fossil record.
A recent development in the debate centers around the discovery of impressions of "protofeathers" surrounding many dinosaur fossils. These protofeathers suggest that the tyrannosauroids may have been feathered.[67] However, others claim that these protofeathers are simply the result of the decomposition of collagenous fiber that underlaid the dinosaurs' integument.[47]
The feathered dinosaurs discovered so far include Beipiaosaurus, Caudipteryx, Dilong, Microraptor, Protarchaeopteryx, Shuvuuia, Sinornithosaurus, Sinosauropteryx, and Jinfengopteryx, along with dinosaur-like birds, such as Confuciusornis, which are anatomically closer to modern avians. All of them have been found in the same area and formation, in northern China. The Dromaeosauridae family, in particular, seems to have been heavily feathered and at least one dromaeosaurid, Cryptovolans, may have been capable of flight.
Because feathers are often associated with birds, feathered dinosaurs are often touted as the missing link between birds and dinosaurs. However, the multiple skeletal features also shared by the two groups represent the more important link for paleontologists. Furthermore, it is increasingly clear that the relationship between birds and dinosaurs, and the evolution of flight, are more complex topics than previously realized. For example, while it was once believed that birds evolved from dinosaurs in one linear progression, some scientists, most notably Gregory S. Paul, conclude that dinosaurs such as the dromaeosaurs may have evolved from birds, losing the power of flight while keeping their feathers in a manner similar to the modern ostrich and other ratites.
Comparisons of bird and dinosaur skeletons, as well as cladistic analysis, strengthens the case for the link, particularly for a branch of theropods called maniraptors. Skeletal similarities include the neck, pubis, wrist (semi-lunate carpal), arm and pectoral girdle, shoulder blade, clavicle, and breast bone.
Large meat-eating dinosaurs had a complex system of air sacs similar to those found in modern birds, according to an investigation which was led by Patrick M. O'Connor of Ohio University. The lungs of theropod dinosaurs (carnivores that walked on two legs and had birdlike feet) likely pumped air into hollow sacs in their skeletons, as is the case in birds. "What was once formally considered unique to birds was present in some form in the ancestors of birds", O'Connor said. The study was funded in part by the National Science Foundation.[68][69]
Computed tomography (CT) scans conducted in 2000 of the chest cavity of a specimen of the ornithopod Thescelosaurus found the apparent remnants of complex four-chambered hearts, much like those found in today's mammals and birds.[70] The idea is controversial within the scientific community, coming under fire for bad anatomical science[71] or simply wishful thinking.[72]
A study published in 2011 applied multiple lines of inquiry to the question of the object's identity, including more advanced CT scanning, histology, X-ray diffraction, X-ray photoelectron spectroscopy, and scanning electron microscopy. From these methods, the authors found that: the object's internal structure does not include chambers but is made up of three unconnected areas of lower density material, and is not comparable to the structure of an ostrich's heart; the "walls" are composed of sedimentary minerals not known to be produced in biological systems, such as goethite, feldspar minerals, quartz, and gypsum, as well as some plant fragments; carbon, nitrogen, and phosphorus, chemical elements important to life, were lacking in their samples; and cardiac cellular structures were absent. There was one possible patch with animal cellular structures. The authors found their data supported identification as a concretion of sand from the burial environment, not the heart, with the possibility that isolated areas of tissues were preserved.[73]
The question of how this find reflects metabolic rate and dinosaur internal anatomy is moot, though, regardless of the object's identity.[73] Both modern crocodilians and birds, the closest living relatives of dinosaurs, have four-chambered hearts (albeit modified in crocodilians), so dinosaurs probably had them as well; the structure is not necessarily tied to metabolic rate.[74]
Fossils of the troodonts Mei and Sinornithoides demonstrate that the dinosaurs slept like certain modern birds, with their heads tucked under their arms.[75] This behavior, which may have helped to keep the head warm, is also characteristic of modern birds.
When laying eggs, female birds grow a special type of bone in their limbs. This medullary bone, which is rich in calcium, forms a layer inside the hard outer bone that is used to make eggshells. The presence of endosteally derived bone tissues lining the interior marrow cavities of portions of a Tyrannosaurus rex specimen's hind limb suggested that T. rex used similar reproductive strategies, and revealed the specimen to be female.[76] Further research has found medullary bone in the theropod Allosaurus and ornithopod Tenontosaurus. Because the line of dinosaurs that includes Allosaurus and Tyrannosaurus diverged from the line that led to Tenontosaurus very early in the evolution of dinosaurs, this suggests that dinosaurs in general produced medullary tissue.[77]
Several Citipati specimens have been found resting over the eggs in its nest in a position most reminiscent of brooding.[78]
Numerous dinosaur species, for example Maiasaura, have been found in herds mixing both very young and adult individuals, suggesting rich interactions between them.
A dinosaur embryo was found without teeth, which suggests some parental care was required to feed the young dinosaur, possibly the adult dinosaur regurgitated food into the young dinosaur's mouth (see altricial). This behaviour is seen in numerous bird species; parent birds regurgitate food into the hatchling's mouth.
Both birds and dinosaurs use gizzard stones. These stones are swallowed by animals to aid digestion and break down food and hard fibres once they enter the stomach. When found in association with fossils, gizzard stones are called gastroliths.[79] Gizzard stones are also found in some fish (mullets, mud shad, and the gilaroo, a type of trout) and in crocodiles.
One of the best examples of soft tissue impressions in a fossil dinosaur was discovered in Petraroia, Italy. The discovery was reported in 1998, and described the specimen of a small, very young coelurosaur, Scipionyx samniticus. The fossil includes portions of the intestines, colon, liver, muscles, and windpipe of this immature dinosaur.[80]
In the March 2005 issue of Science, Dr. Mary Higby Schweitzer and her team announced the discovery of flexible material resembling actual soft tissue inside a 68-million-year-old Tyrannosaurus rex leg bone from the Hell Creek Formation in Montana. After recovery, the tissue was rehydrated by the science team. The seven collagen types obtained from the bone fragments, compared to collagen data from living birds (specifically, a chicken), suggest that older theropods and birds are closely related.
When the fossilized bone was treated over several weeks to remove mineral content from the fossilized bone marrow cavity (a process called demineralization), Schweitzer found evidence of intact structures such as blood vessels, bone matrix, and connective tissue (bone fibers). Scrutiny under the microscope further revealed that the putative dinosaur soft tissue had retained fine structures (microstructures) even at the cellular level. The exact nature and composition of this material, and the implications of Dr. Schweitzer's discovery, are not yet clear; study and interpretation of the specimens is ongoing.[81]
The successful extraction of ancient DNA from dinosaur fossils has been reported on two separate occasions, but upon further inspection and peer review, neither of these reports could be confirmed.[82] However, a functional visual peptide of a theoretical dinosaur has been inferred using analytical phylogenetic reconstruction methods on gene sequences of related modern species such as reptiles and birds.[83] In addition, several proteins have putatively been detected in dinosaur fossils,[84] including hemoglobin.[85]
Debates about the origin of bird flight are almost as old as the idea that birds evolved from dinosaurs, which arose soon after the discovery of Archaeopteryx in 1862. Two theories have dominated most of the discussion since then: the cursorial ("from the ground up") theory proposes that birds evolved from small, fast predators that ran on the ground; the arboreal ("from the trees down") theory proposes that powered flight evolved from unpowered gliding by arboreal (tree-climbing) animals. A more recent theory, "wing-assisted incline running" (WAIR), is a variant of the cursorial theory and proposes that wings developed their aerodynamic functions as a result of the need to run quickly up very steep slopes, for example to escape from predators.
The cursorial theory of the origin of flight was first proposed by Samuel Wendell Williston, and elaborated upon by Baron Nopcsa. This hypothesis proposes that some fast-running animals with long tails used their arms to keep their balance while running. Modern versions of this theory differ in many details from the Williston-Nopcsa version, mainly as a result of discoveries since Nopcsa's time.
Nopcsa theorized that increasing the surface area of the outstretched arms could have helped small cursorial predators to keep their balance, and that the scales of the forearms became elongated, evolving into feathers. The feathers could also have been used as a trap to catch insects or other prey. Progressively, the animals would have leapt for longer distances, helped by their evolving wings. Nopcsa also proposed that there were three main stages in the evolution of flight. First, passive flight was realized, in which the developed wing structures served as a sort of parachute. Second, active flight was possible, in which the animal achieved flight by flapping its wings. He used Archaeopteryx as an example of this second stage. Finally, birds gained the ability to soar.[86]
It is now thought that feathers did not evolve from scales, as feathers are made of different proteins.[87] More seriously, Nopcsa's theory assumes that feathers evolved as part of the evolution of flight, and recent discoveries prove that assumption is false.
Feathers are very common in coelurosaurian dinosaurs (including the early tyrannosauroid Dilong).[88] Modern birds are classified as coelurosaurs by nearly all palaeontologists,[89] though not by a few ornithologists.[90][91] The modern version of the "from the ground up" hypothesis argues that birds' ancestors were small, feathered, ground-running predatory dinosaurs (rather like roadrunners in their hunting style[92]) that used their forelimbs for balance while pursuing prey, and that the forelimbs and feathers later evolved in ways that provided gliding and then powered flight. The most widely suggested original functions of feathers include thermal insulation and competitive displays, as in modern birds.[93][94]
All of the Archaeopteryx fossils come from marine sediments, and it has been suggested that wings may have helped the birds run over water in the manner of the Jesus Christ Lizard (Common basilisk).[95]
Most recent refutations of the "from the ground up" hypothesis attempt to refute the modern version's assumption that birds are modified coelurosaurian dinosaurs. The strongest attacks are based on embryological analyses which conclude that birds' wings are formed from digits 2, 3, and 4 (corresponding to the index, middle, and ring fingers in humans; the first of a bird's three digits forms the alula, which they use to avoid stalling in low-speed flight, for example when landing); but the hands of coelurosaurs are formed by digits 1, 2, and 3 (thumb and first two fingers in humans).[96] However, these embryological analyses were immediately challenged on the embryological grounds that the "hand" often develops differently in clades that have lost some digits in the course of their evolution, and that birds' "hands" do develop from digits 1, 2, and 3.[97][98][98] This debate is complex and not yet resolved - see "Digit homology" below.
The WAIR hypothesis was prompted by observation of young chukar chicks, and proposes that wings developed their aerodynamic functions as a result of the need to run quickly up very steep slopes such as tree trunks, for example to escape from predators.[99] This makes it a specialized type of cursorial ("from the ground up") theory. Note that in this scenario birds need downforce to give their feet increased grip.[100][101] But early birds, including Archaeopteryx, lacked the shoulder mechanism by which modern birds' wings produce swift, powerful upstrokes; since the downforce on which WAIR depends is generated by upstrokes, it seems that early birds were incapable of WAIR.[102] Because WAIR is a behavioural trait without osteological specializations, the phylogenetic placement of the flight stroke before the divergence of Neornithes makes it impossible to determine if WAIR is ancestral to the avian flight stroke or derived from it.[103]
Most versions of the arboreal hypothesis state that the ancestors of birds were very small dinosaurs that lived in trees, springing from branch to branch. This small dinosaur already had feathers, which were co-opted by evolution to produce longer, stiffer forms that were useful in aerodynamics, eventually producing wings. Wings would have then evolved and become increasingly refined as devices to give the leaper more control, to parachute, to glide, and to fly in stepwise fashion. The arboreal hypothesis also notes that, for arboreal animals, aerodynamics are far more energy efficient, since such animals simply fall in order to achieve minimum gliding speeds.[104][105]
Several small dinosaurs from the Jurassic or Early Cretaceous, all with feathers, have been interpreted as possibly having arboreal and/or aerodynamic adaptations. These include Scansoriopteryx, Epidexipteryx, Microraptor, Pedopenna, and Anchiornis. Anchiornis is particularly important to this subject, as it lived at the beginning of the Late Jurassic, long before Archaeopteryx.[106]
Analysis of the proportions of the toe bones of the most primitive birds Archaeopteryx and Confuciusornis, compared to those of living species, suggest that the early species may have lived both on the ground and in trees.[107]
One study suggested that the earliest birds and their immediate ancestors did not climb trees. This study determined that the amount of toe claw curvature of early birds was more like that seen in modern ground-foraging birds than in perching birds.[108]
Archaeopteryx was the first and for a long time the only known feathered Mesozoic animal (or dinosaur, if one accepts the majority view that birds are modified dinosaurs). As a result, discussion of the evolution of birds and of bird flight centered on Archaeopteryx at least until the mid-1990s.
There has been debate about whether Archaeopteryx could really fly. It appears that Archaeopteryx had the brain structures and inner-ear balance sensors that birds use to control their flight.[109] Archaeopteryx also had a wing feather arrangement like that of modern birds and similarly asymmetrical flight feathers on its wings and tail. But Archaeopteryx lacked the shoulder mechanism by which modern birds' wings produce swift, powerful upstrokes (see diagram above of supracoracoideus pulley); this may mean that it and other early birds were incapable of flapping flight and could only glide.[102]
But the discovery since the early 1990s of many feathered dinosaurs means that Archaeopteryx is no longer the key figure in the evolution of bird flight. Other small, feathered coelurosaurs from the Cretaceous and Late Jurassic show features that may be precursors of avian flight, for example: Rahonavis, a ground-runner which had a Velociraptor-like raised sickle claw on the second toe and which some paleontologists think was better adapted for flight than Archaeopteryx;[110] Scansoriopteryx, an arboreal dinosaur that may provide some support for the "from the trees down" theory;[111] Microraptor, an arboreal dinosaur that may have been capable of powered flight but, if so, more like a biplane, as it had well-developed feathers on its legs.[112] As early as 1915, some scientists had argued that the evolution of bird flight may have gone through a four-winged (or tetrapteryx) stage.[113][114]
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A hypothesis, credited to Gregory Paul and propounded in his books Predatory Dinosaurs of the World (1988) and Dinosaurs of the Air (2002), suggests that some groups of non-flying carnivorous dinosaurs, especially deinonychosaurs but perhaps others such as oviraptorosaurs, therizinosaurs, alvarezsaurids and ornithomimosaurs, are actually descended from birds. Paul also proposed that the bird ancestor of these groups was more advanced in its flight adaptations than Archaeopteryx. This would mean that Archaeopteryx is thus less closely related to extant birds than these dinosaurs are.[115]
Paul's hypothesis received additional support when Mayr et al. (2005) analyzed a new, tenth specimen of Archaeopteryx, and concluded that Archaeopteryx was the sister clade to the Deinonychosauria, but that the more advanced bird Confuciusornis was within the Dromaeosauridae. This result supports Paul's hypothesis, suggesting that the Deinonychosauria and the Troodontidae are part of Aves, the bird lineage proper, and secondarily flightless.[116] This paper, however, excluded all other birds and thus did not sample their character distributions. The paper was criticized by Corfe and Butler (2006) who found the authors could not support their conclusions statistically. Mayr et al. agreed that the statistical support was weak, but added that it is also weak for the alternative scenarios.[117]
Paul's hypothesis about the position of Archaeopteryx is not supported by current cladistic analyses which generally find that Archaeopteryx is closer to birds, within the clade Avialae, than it is to deinonychosaurs or oviraptorosaurs. However, the version of this theory stating that some non-flying carnivorous dinosaurs may have had flying ancestors is supported by some fossils. Especially, Microraptor, Pedopenna, and Anchiornis all have winged feet, share many features, and lie close to the base of the clade Paraves. This suggests that the ancestral paravian was a four-winged glider, and that larger Deinonychosaurs secondarily lost the ability to glide, while the bird lineage increased in aerodynamic ability as it progressed.[2]
There is a debate between embryologists and paleontologists whether the hands of theropod dinosaurs and birds are essentially different, based on phalangeal counts, a count of the number of phalanges (fingers) in the hand. This is an important and fiercely debated area of research because its results may challenge the consensus that birds are descendants of dinosaurs.
Embryologists and some paleontologists who oppose the bird-dinosaur link, have long numbered the digits of birds II-III-IV on the basis of multiple studies of the development in the egg.[118][119][120] [121][122] This is based on the fact that in most amniotes, the first digit to form in a 5-fingered hand is digit IV, which develops a primary axis. Therefore, embryologists have identified the primary axis in birds as digit IV, and the surviving digits as II-III-IV. The fossils of advanced theropod (Tetanurae) hands appear to have the digits I-II-III (some genera within Avetheropoda also have a reduced digit IV[123]). If this is true, then the II-III-IV development of digits in birds is an indication against theropod (dinosaur) ancestry. However, with no ontogenical (developmental) basis to definitively state which digits are which on a theropod hand (because no non-avian theropods can be observed growing and developing today), the labelling of the theropod hand is not absolutely conclusive.
Paleontologists have traditionally identified avian digits as I-II-III. They argue that the digits of birds number I-II-III, just as those of theropod dinosaurs do, by the conserved phalangeal formula. The phalangeal count for archosaurs is 2-3-4-5-3; many archosaur lineages have a reduced number of digits, but have the same phalangeal formula in the digits that remain. In other words, paleontologists assert that archosaurs of different lineages tend to lose the same digits when digit loss occurs, from the outside to the inside. The three digits of dromaeosaurs, and Archaeopteryx have the same phalangeal formula of I-II-III as digits I-II-III of basal archosaurs. Therefore, the lost digits would be V and IV. If this is true, then modern birds would also possess digits I-II-III.[122] Also, one research team has proposed a frame-shift in the digits of the theropod line leading to birds (thus making digit I into digit II, II to III, and so forth).[124][125] However, such frame shifts are rare in amniotes and would have had to occur solely in the forelimbs and not the hindlimbs (a condition presently unknown in any animal) in the bird-theropod lineage in order to be consistent with the theropod origin of birds.[126] This is called Lateral Digit Reduction (LDR) versus Bilateral Digit Reduction (BDR) (see also Limusaurus[127])