Dinosaur: For Other Uses, See
Dinosaur: For Other Uses, See
Dinosaurs
Temporal range: Late TriassicPresent, 231.4 0 Mya
Pre
Pg
N
A collection of fossil dinosaur skeletons. Clockwise from
armored ankylosaur)
Scientific classification
Kingdom: Animalia
Phylum: Chordata
Clade: Dinosauriformes
Clade: Dinosauria
Owen, 1842
Major groups
Ornithischia
Heterodontosauridae
Genasauria
Neornithischia
Thyreophora
Saurischia
Sauropodomorpha
Theropoda
Dinosaurs are a diverse group of reptiles[note 1] of the clade Dinosauria that first appeared during
the Triassic period. Although the exact origin and timing of the evolution of dinosaurs is the subject
of active research,[1] the current scientific consensus places their origin between 231 and 243 million
years ago.[2] They became the dominant terrestrial vertebrates after the TriassicJurassic extinction
event 201 million years ago. Their dominance continued through
the Jurassic and Cretaceousperiods and ended when the CretaceousPaleogene extinction
event led to the extinction of most dinosaur groups 66 million years ago.
The fossil record indicates that birds are modern feathered dinosaurs,[3] having evolved
from theropod ancestors during the Jurassic Period.[4] As such, birds were the only dinosaur lineage
to survive the mass extinction event.[5] Throughout the remainder of this article, the term "dinosaur" is
sometimes used generically to refer to the combined group of avian dinosaurs (birds) and non-avian
dinosaurs (all other dinosaurs); at other times it is used to refer to the non-avian dinosaurs
specifically, while the avian dinosaurs are sometimes simply referred to as "birds". This article deals
primarily with non-avian dinosaurs.
Dinosaurs are a varied group of animals from taxonomic, morphological and ecological standpoints.
Birds, at over 10,000 living species,[6] are the most diverse group of vertebrates
besides perciform fish.[7] Using fossil evidence, paleontologists have identified over 500
distinct genera[8] and more than 1,000 different species of non-avian dinosaurs.[9] Dinosaurs are
represented on every continent by both extant species (birds) and fossil remains.[10] Through the first
half of the 20th century, before birds were recognized to be dinosaurs, most of the scientific
community believed dinosaurs to have been sluggish and cold-blooded. Most research conducted
since the 1970s, however, has indicated that all dinosaurs were active animals with
elevated metabolisms and numerous adaptations for social interaction. Some are herbivorous,
others carnivorous. Evidence suggests that egg laying and nest building are additional traits shared
by all dinosaurs.
While dinosaurs were ancestrally bipedal, many extinct groups included quadrupedal species, and
some were able to shift between these stances. Elaborate display structures such as horns or crests
are common to all dinosaur groups, and some extinct groups developed skeletal modifications such
as bony armor and spines. While the dinosaurs' modern-day surviving avian lineage (birds) are
generally small due to the constraints of flight, many prehistoric dinosaurs (non-avian and avian)
were large-bodiedthe largest sauropod dinosaurs are estimated to have reached lengths of 39.7
meters (130 feet)[11] and heights of 18 meters (59 feet)[12] and were the largest land animals of all
time. Still, the idea that non-avian dinosaurs were uniformly gigantic is a misconception based in part
on preservation bias, as large, sturdy bones are more likely to last until they are fossilized. Many
dinosaurs were quite small: Xixianykus, for example, was only about 50 cm (20 in) long.
Since the first dinosaur fossils were recognized in the early 19th century, mounted fossil dinosaur
skeletons have been major attractions at museums around the world, and dinosaurs have become
an enduring part of world culture. The large sizes of some dinosaur groups, as well as their
seemingly monstrous and fantastic nature, have ensured dinosaurs' regular appearance in best-
selling books and films, such as Jurassic Park. Persistent public enthusiasm for the animals has
resulted in significant funding for dinosaur science, and new discoveries are regularly covered by the
media.
Contents
[hide]
1Etymology
2Definition
o 2.1General description
o 2.2Distinguishing anatomical features
3Evolutionary history
o 3.1Origins and early evolution
o 3.2Evolution and paleobiogeography
4Classification
o 4.1Taxonomy
5Biology
o 5.1Size
5.1.1Largest and smallest
o 5.2Behavior
o 5.3Communication
o 5.4Reproductive biology
o 5.5Physiology
6Origin of birds
o 6.1Feathers
o 6.2Skeleton
o 6.3Soft anatomy
o 6.4Behavioral evidence
7Extinction of major groups
o 7.1Impact event
o 7.2Deccan Traps
o 7.3Possible Paleocene survivors
8History of study
o 8.1"Dinosaur renaissance"
o 8.2Soft tissue and DNA
9Cultural depictions
10See also
11Notes
12References
13Further reading
14External links
Etymology
The taxon Dinosauria was formally named in 1842 by paleontologist Sir Richard Owen, who used it
to refer to the "distinct tribe or sub-order of Saurian Reptiles" that were then being recognized in
England and around the world.[13] The term is derived from the Greek words (deinos, meaning
"terrible", "potent", or "fearfully great") and (sauros, meaning "lizard" or "reptile").[13][14] Though
the taxonomic name has often been interpreted as a reference to dinosaurs' teeth, claws, and other
fearsome characteristics, Owen intended it merely to evoke their size and majesty.[15]
Other prehistoric animals, including mosasaurs, ichthyosaurs, pterosaurs, plesiosaurs,
and Dimetrodon, while often popularly conceived of as dinosaurs, are not taxonomically classified as
dinosaurs.
Definition
Using one of the above definitions, dinosaurs can be generally described as archosaurs with hind
limbs held erect beneath the body.[22] Many prehistoric animal groups are popularly conceived of as
dinosaurs, such as ichthyosaurs, mosasaurs, plesiosaurs, pterosaurs,
and pelycosaurs (especially Dimetrodon), but are not classified scientifically as dinosaurs, and none
had the erect hind limb posture characteristic of true dinosaurs.[23] Dinosaurs were the dominant
terrestrial vertebrates of the Mesozoic, especially the Jurassic and Cretaceous periods. Other
groups of animals were restricted in size and niches; mammals, for example, rarely exceeded the
size of a domestic cat, and were generally rodent-sized carnivores of small prey.[24]
Dinosaurs have always been an extremely varied group of animals; according to a 2006 study, over
500 non-avian dinosaur genera have been identified with certainty so far, and the total number of
genera preserved in the fossil record has been estimated at around 1850, nearly 75% of which
remain to be discovered.[8] An earlier study predicted that about 3400 dinosaur genera existed,
including many that would not have been preserved in the fossil record.[25] By September 17, 2008,
1047 different species of dinosaurs had been named.[9]
In 2016, the estimated number of dinosaur species that existed in the Mesozoic era was estimated
to be 1,5432,468.[26][27] Some are herbivorous, others carnivorous, including seed-eaters, fish-eaters,
insectivores, and omnivores. While dinosaurs were ancestrally bipedal (as are all modern birds),
some prehistoric species were quadrupeds, and others, such as Ammosaurus and Iguanodon, could
walk just as easily on two or four legs. Cranial modifications like horns and crests are common
dinosaurian traits, and some extinct species had bony armor. Although known for large size, many
Mesozoic dinosaurs were human-sized or smaller, and modern birds are generally small in size.
Dinosaurs today inhabit every continent, and fossils show that they had achieved global distribution
by at least the early Jurassic period.[10] Modern birds inhabit most available habitats, from terrestrial
to marine, and there is evidence that some non-avian dinosaurs (such as Microraptor) could fly or at
least glide, and others, such as spinosaurids, had semi-aquatic habits.[28]
Distinguishing anatomical features
While recent discoveries have made it more difficult to present a universally agreed-upon list of
dinosaurs' distinguishing features, nearly all dinosaurs discovered so far share certain modifications
to the ancestral archosaurian skeleton, or are clear descendants of older dinosaurs showing these
modifications. Although some later groups of dinosaurs featured further modified versions of these
traits, they are considered typical for Dinosauria; the earliest dinosaurs had them and passed them
on to their descendants. Such modifications, originating in the most recent common ancestor of a
certain taxonomic group, are called the synapomorphies of such a group.[29]
A detailed assessment of archosaur interrelations by Sterling Nesbitt[30] confirmed or found the
following twelve unambiguous synapomorphies, some previously known:
in the skull, a supratemporal fossa (excavation) is present in front of the supratemporal fenestra,
the main opening in the rear skull roof
epipophyses, obliquely backward pointing processes on the rear top corners, present in the
anterior (front) neck vertebrae behind the atlas and axis, the first two neck vertebrae
apex of deltopectoral crest (a projection on which the deltopectoral muscles attach) located at or
more than 30% down the length of the humerus (upper arm bone)
radius, a lower arm bone, shorter than 80% of humerus length
fourth trochanter (projection where the caudofemoralis muscle attaches on the inner rear shaft)
on the femur (thighbone) is a sharp flange
fourth trochanter asymmetrical, with distal, lower, margin forming a steeper angle to the shaft
on the astragalus and calcaneum, upper ankle bones, the proximal articular facet, the top
connecting surface, for the fibula occupies less than 30% of the transverse width of the element
exoccipitals (bones at the back of the skull) do not meet along the midline on the floor of the
endocranial cavity, the inner space of the braincase
in the pelvis, the proximal articular surfaces of the ischium with the ilium and the pubis are
separated by a large concave surface (on the upper side of the ischium a part of the open hip
joint is located between the contacts with the pubic bone and the ilium)
cnemial crest on the tibia (protruding part of the top surface of the shinbone) arcs anterolaterally
(curves to the front and the outer side)
distinct proximodistally oriented (vertical) ridge present on the posterior face of the distal end of
the tibia (the rear surface of the lower end of the shinbone)
concave articular surface for the fibula of the calcaneum (the top surface of the calcaneum,
where it touches the fibula, has a hollow profile)
Nesbitt found a number of further potential synapomorphies, and discounted a number of
synapomorphies previously suggested. Some of these are also present in silesaurids, which Nesbitt
recovered as a sister group to Dinosauria, including a large anterior trochanter, metatarsals II and IV
of subequal length, reduced contact between ischium and pubis, the presence of a cnemial crest on
the tibia and of an ascending process on the astragalus, and many others.[16]
A variety of other skeletal features are shared by dinosaurs. However, because they are either
common to other groups of archosaurs or were not present in all early dinosaurs, these features are
not considered to be synapomorphies. For example, as diapsids, dinosaurs ancestrally had two pairs
of temporal fenestrae (openings in the skull behind the eyes), and as members of the diapsid group
Archosauria, had additional openings in the snout and lower jaw.[31] Additionally, several
characteristics once thought to be synapomorphies are now known to have appeared before
dinosaurs, or were absent in the earliest dinosaurs and independently evolved by different dinosaur
groups. These include an elongated scapula, or shoulder blade; a sacrum composed of three or
more fused vertebrae (three are found in some other archosaurs, but only two are found
in Herrerasaurus);[16] and a perforate acetabulum, or hip socket, with a hole at the center of its inside
surface (closed in Saturnalia, for example).[32][33] Another difficulty of determining distinctly
dinosaurian features is that early dinosaurs and other archosaurs from the late Triassic are often
poorly known and were similar in many ways; these animals have sometimes been misidentified in
the literature.[34]
Hip joints and hindlimb postures of: (left to right) typical reptiles (sprawling), dinosaurs and mammals (erect),
and rauisuchians (erect)
Dinosaurs stand with their hind limbs erect in a manner similar to most modern mammals, but
distinct from most other reptiles, whose limbs sprawl out to either side.[35] This posture is due to the
development of a laterally facing recess in the pelvis (usually an open socket) and a corresponding
inwardly facing distinct head on the femur.[36] Their erect posture enabled early dinosaurs to breathe
easily while moving, which likely permitted stamina and activity levels that surpassed those of
"sprawling" reptiles.[37] Erect limbs probably also helped support the evolution of large size by
reducing bending stresses on limbs.[38] Some non-dinosaurian archosaurs, including rauisuchians,
also had erect limbs but achieved this by a "pillar erect" configuration of the hip joint, where instead
of having a projection from the femur insert on a socket on the hip, the upper pelvic bone was
rotated to form an overhanging shelf.[38]
Evolutionary history
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Orange labels: known ice ages.
Also see: Human timeline and Nature timeline
By the early Cretaceous and the ongoing breakup of Pangaea, dinosaurs were becoming strongly
differentiated by landmass. The earliest part of this time saw the spread of
ankylosaurians, iguanodontians, and brachiosaurids through Europe, North America, and northern
Africa. These were later supplemented or replaced in Africa by
large spinosauridand carcharodontosaurid theropods,
and rebbachisaurid and titanosaurian sauropods, also found in South America. In Asia, maniraptoran
coelurosaurians like dromaeosaurids, troodontids, and oviraptorosaurians became the common
theropods, and ankylosaurids and early ceratopsians like Psittacosaurus became important
herbivores. Meanwhile, Australia was home to a fauna of basal ankylosaurians, hypsilophodonts,
and iguanodontians.[48] The stegosaurians appear to have gone extinct at some point in the late early
Cretaceous or early late Cretaceous. A major change in the early Cretaceous, which would be
amplified in the late Cretaceous, was the evolution of flowering plants. At the same time, several
groups of dinosaurian herbivores evolved more sophisticated ways to orally process food.
Ceratopsians developed a method of slicing with teeth stacked on each other in batteries, and
iguanodontians refined a method of grinding with tooth batteries, taken to its extreme
in hadrosaurids.[49] Some sauropods also evolved tooth batteries, best exemplified by the
rebbachisaurid Nigersaurus.[51]
There were three general dinosaur faunas in the late Cretaceous. In the northern continents of North
America and Asia, the major theropods were tyrannosaurids and various types of smaller
maniraptoran theropods, with a predominantly ornithischian herbivore assemblage of hadrosaurids,
ceratopsians, ankylosaurids, and pachycephalosaurians. In the southern continents that had made
up the now-splitting Gondwana, abelisaurids were the common theropods, and titanosaurian
sauropods the common herbivores. Finally, in Europe,
dromaeosaurids, rhabdodontid iguanodontians, nodosaurid ankylosaurians, and titanosaurian
sauropods were prevalent.[48] Flowering plants were greatly radiating,[49]with the first grasses
appearing by the end of the Cretaceous.[52] Grinding hadrosaurids and shearing ceratopsians
became extremely diverse across North America and Asia. Theropods were also radiating as
herbivores or omnivores, with therizinosaurians and ornithomimosaurians becoming common.[49]
The CretaceousPaleogene extinction event, which occurred approximately 66 million years ago at
the end of the Cretaceous period, caused the extinction of all dinosaur groups except for
the neornithine birds. Some other diapsid groups, such as
crocodilians, sebecosuchians, turtles, lizards, snakes, sphenodontians, and choristoderans, also
survived the event.[53]
The surviving lineages of neornithine birds, including the ancestors of modern ratites, ducks and
chickens, and a variety of waterbirds, diversified rapidly at the beginning of the Paleogene period,
entering ecological niches left vacant by the extinction of Mesozoic dinosaur groups such as the
arboreal enantiornithines, aquatic hesperornithines, and even the larger terrestrial theropods (in the
form of Gastornis, eogruiids, bathornithids, ratites, geranoidids, mihirungs, and "terror birds"). It is
often cited that mammals out-competed the neornithines for dominance of most terrestrial niches but
many of these groups co-existed with rich mammalian faunas for most of the Cenozoic.[54] Terror
birds and bathornithids occupied carnivorous guilds alongside predatory mammals,[55][56] and ratites
are still being fairly successful as mid-sized herbivores; eogruiids similarly lasted from the Eocene
to Pliocene, only becoming extinct very recently after over 20 million years of co-existence with
many mammal groups.[57]
Classification