There is significant evidence that birds evolved from theropod dinosaurs, specifically, that birds are members of Maniraptora, a group of theropods which includes dromaeosaurs and oviraptorids, among others.[1] As more non-avian theropods that are closely related to birds are discovered, the formerly clear distinction between non-birds and birds becomes less so. Recent discoveries in northeast China (Liaoning Province), demonstrating that many small theropod dinosaurs had feathers, contribute to this ambiguity.
The basal bird Archaeopteryx, from the Jurassic, is well-known as one of the first "missing links" to be found in support of evolution in the late 19th century, though it is not considered a direct ancestor of modern birds. Confuciusornis is another early bird; it lived in the Early Cretaceous. Both may be predated by Protoavis texensis, though the fragmentary nature of this fossil leaves it open to considerable doubt if this was a bird ancestor. Other Mesozoic birds include the Enantiornithes, Yanornis, Ichthyornis, Gansus and the Hesperornithiformes, a group of flightless divers resembling grebes and loons.
The recently (2002) discovered dromaeosaur Cryptovolans was capable of powered flight, possessed a sternal keel and had ribs with uncinate processes. In fact, Cryptovolans makes a better "bird" than Archaeopteryx which is missing some of these modern bird features. Because of this, some paleontologists have suggested that dromaeosaurs are actually basal birds whose larger members are secondarily flightless, i.e. that dromaeosaurs evolved from birds and not the other way around. Evidence for this theory is currently inconclusive, but digs continue to unearth fossils (especially in China) of the strange feathered dromaeosaurs. At any rate, it is fairly certain that avian flight existed in the mid-Jurassic and was "tried out" in several lineages and variants by the mid-Cretaceous.
Although ornithischian (bird-hipped) dinosaurs share the same hip structure as birds, birds actually originated from the saurischian (lizard-hipped) dinosaurs (if the dinosaurian origin theory is correct), and thus arrived at their hip structure condition independently. In fact, the bird-like hip structure also developed a third time among a peculiar group of theropods, the Therizinosauridae.
An alternate theory to the dinosaurian origin of birds, espoused by a few scientists (most notably Lary Martin and Alan Feduccia), states that birds (including maniraptoran "dinosaurs") evolved from early archosaurs like Longisquama, a theory which is contested by most other scientists in paleontology, and by experts in feather development and evolution such as R.O. Prum. See the Longisquama article for more on this alternative.
Modern birds are classified in Neornithes, which are now known to have evolved into some basic lineages by the end of the Cretaceous (see Vegavis). The Neornithes are split into the Paleognathae and Neognathae. The paleognaths include the tinamous (found only in Central and South America) and the ratites. The ratites are large flightless birds, and include ostriches, cassowaries, kiwis and emus (though some scientists suspect that the ratites represent an artificial grouping of birds which have independently lost the ability to fly in a number of unrelated lineages). The basal divergence from the remaining Neognathes was that of the Galloanseri, the superorder containing the Anseriformes (ducks, geese and swans), and the Galliformes (the pheasants, grouse, and their allies). See the chart for more information.
The classification of birds is a contentious issue. Sibley & Ahlquist's Phylogeny and Classification of Birds (1990) is a landmark work on the classification of birds (although frequently debated and constantly revised). A preponderance of evidence seems to suggest that the modern bird orders constitute accurate taxa. However, scientists are not in agreement as to the relationships between the orders; evidence from modern bird anatomy, fossils and DNA have all been brought to bear on the problem but no strong consensus has emerged. More recently, new fossil and molecular evidence is providing an increasingly clear picture of the evolution of modern bird orders. See also: Sibley-Ahlquist taxonomy.
The basal bird Archaeopteryx, from the Jurassic, is well-known as one of the first "missing links" to be found in support of evolution in the late 19th century, though it is not considered a direct ancestor of modern birds. Confuciusornis is another early bird; it lived in the Early Cretaceous. Both may be predated by Protoavis texensis, though the fragmentary nature of this fossil leaves it open to considerable doubt if this was a bird ancestor. Other Mesozoic birds include the Enantiornithes, Yanornis, Ichthyornis, Gansus and the Hesperornithiformes, a group of flightless divers resembling grebes and loons.
The recently (2002) discovered dromaeosaur Cryptovolans was capable of powered flight, possessed a sternal keel and had ribs with uncinate processes. In fact, Cryptovolans makes a better "bird" than Archaeopteryx which is missing some of these modern bird features. Because of this, some paleontologists have suggested that dromaeosaurs are actually basal birds whose larger members are secondarily flightless, i.e. that dromaeosaurs evolved from birds and not the other way around. Evidence for this theory is currently inconclusive, but digs continue to unearth fossils (especially in China) of the strange feathered dromaeosaurs. At any rate, it is fairly certain that avian flight existed in the mid-Jurassic and was "tried out" in several lineages and variants by the mid-Cretaceous.
Although ornithischian (bird-hipped) dinosaurs share the same hip structure as birds, birds actually originated from the saurischian (lizard-hipped) dinosaurs (if the dinosaurian origin theory is correct), and thus arrived at their hip structure condition independently. In fact, the bird-like hip structure also developed a third time among a peculiar group of theropods, the Therizinosauridae.
An alternate theory to the dinosaurian origin of birds, espoused by a few scientists (most notably Lary Martin and Alan Feduccia), states that birds (including maniraptoran "dinosaurs") evolved from early archosaurs like Longisquama, a theory which is contested by most other scientists in paleontology, and by experts in feather development and evolution such as R.O. Prum. See the Longisquama article for more on this alternative.
Modern birds are classified in Neornithes, which are now known to have evolved into some basic lineages by the end of the Cretaceous (see Vegavis). The Neornithes are split into the Paleognathae and Neognathae. The paleognaths include the tinamous (found only in Central and South America) and the ratites. The ratites are large flightless birds, and include ostriches, cassowaries, kiwis and emus (though some scientists suspect that the ratites represent an artificial grouping of birds which have independently lost the ability to fly in a number of unrelated lineages). The basal divergence from the remaining Neognathes was that of the Galloanseri, the superorder containing the Anseriformes (ducks, geese and swans), and the Galliformes (the pheasants, grouse, and their allies). See the chart for more information.
The classification of birds is a contentious issue. Sibley & Ahlquist's Phylogeny and Classification of Birds (1990) is a landmark work on the classification of birds (although frequently debated and constantly revised). A preponderance of evidence seems to suggest that the modern bird orders constitute accurate taxa. However, scientists are not in agreement as to the relationships between the orders; evidence from modern bird anatomy, fossils and DNA have all been brought to bear on the problem but no strong consensus has emerged. More recently, new fossil and molecular evidence is providing an increasingly clear picture of the evolution of modern bird orders. See also: Sibley-Ahlquist taxonomy.
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