The Zords of Power Rangers Dino Thunder were dinosaur-based cyborgs created by Tommy Oliver and Anton Mercer during their collaboration. They were mostly maintained by Tommy's friend Hayley. The Dinozords (first called Biozords), created by Anton Mercer and Tommy Oliver with the rest of their dinosaur-related experiments, they were commandeered by Mesogog. He unleashed the Tyrannozord, Pterazord, and Tricerazord upon the Rangers, but they were taken over by the Dino Thunder Rangers. Other Dinozords were unleashed throughout the series. The Tyrannozord, Tricerazord, Pterazord, and the Mezodon Rover were destroyed battling the Zelzord. The fate of the other Zords was not shown or discussed on screen.
Primary Zords
Tyrannozord: A red Tyrannosaurus Rex Zord that forms the majority of the Thundersaurus Megazord (head, torso, left arm, legs and the Dino Drill), controlled by Conner McKnight the Red Dino Ranger. It was destroyed in the finale.
Tricerazord: A blue Triceratops Zord that forms the right arm and Toro Shield of the Thundersaurus Megazord, controlled by Ethan James the Blue Dino Ranger. It was destroyed in the finale.
Pterazord: A yellow Pteranodon Zord that forms helmet and chestplate of the Thundersaurus Megazord, as well at the Pterarang weapon, controlled by Kira Ford the Yellow Dino Ranger. It was destroyed in the finale.
Brachiozord: A black Brachiosaurus Carrierzord that carries the Tyranno, Tricera, and Ptera Zords, as well as the Auxiliary Zords. Has been shown to fire electric blasts from its mouth. Controlled by Tommy Oliver the Black Dino Ranger. This may be a reference to Titanus the Carrierzord from Mighty Morphin Power Rangers.
Dragozord: A white Tupuxuara Zord that forms arms, legs, and weapons of the Dino Stegazord, and the wings of the Valkasaurus Megazord. Can create gusts of wind by flapping its wings. Controlled by Trent Fernandez the White Dino Ranger. Where it got its name is a mystery since "Drago" means Dragon in Latin.
Mezodon Rover: The personal Zord of the Triassic Ranger, the Mezodon Rover has two forms. One is that of a giant chariot pulled by the "Styracozord" (a crimson colored Styracosaurus zord), called the Triassic Megarover. In the chariot form, the Mezodon Rover's wheels can ignite and be used to ram into enemies. It also was controlled by Tommy (in 'A Test of Trust') and Ethan (in 'Thunder Struck'). It can combine with Cephalozord, Dimetrazord, Parasaurzord and Ankylozord to form Triceramax Megazord. It was destroyed by Ethan to destroy the Zelzord after it was set to self destruct.
Auxiliary Zords
Cephalozord: A violet Pachycephalosaurus Zord that forms the Punch weapon arm (right side) for the Thundersaurus Megazord and Dino Stegazord. It also forms the right arm of the Triceramax Megazord. Usually summoned by Tommy, but can also be controlled by Ethan.
Dimetrozord: A cyan Dimetrodon Zord that forms the Saw weapon arm (left side) for the Thundersaurus Megazord and Dino Stegazord. It also forms the inner right leg of the Triceramax Megazord. Usually summoned by Tommy, but can also be controlled by Kira.
Stegozord: A crimson Stegosaurus Zord that becomes a hovercraft for the Thundersaurus and Valkasaurus Megazord. Helps the Thundersaurus Megazord do a "Surf's Up" slash/drill attack. It forms the body and the head for the Dino Stegazord. Traditionally, it is Trent's Zord but it could also be Tommy's second Zord, seeing as how he entered Dino Stegazord, when he temporarily commanded it, and the Valkasaurus Megazord through the Stegozord.
Parasaurzord: A green Parasaurolophus Zord that forms the Scissor Blade weapon (left side) arm for the Thundersaurus Megazord. It also forms the inner left leg of the Triceramax Megazord. Usually summoned by Tommy, but can be controlled by Kira.
Ankylozord: An orange Ankylosaurus Zord that forms the Shield Drill weapon arm (right side) for the Thundersaurus Megazord. It also forms the left arm of the Triceramax Megazord. Usually summoned by Tommy, but can also be controlled by Ethan.
Replicant Zords
Carnotaur Zord: An indigo-and-teal Carnotaurus Zord that forms the majority of the Blizzard Megazord (head, chest, legs, left arm, and the Blizzard Drill).
Chasmosaur Zord: A silver-and-violet Chasmosaurus Zord that forms the right arm and the Blizzard Shield of the Blizzard Megazord.
CAUTION... this blog may contain some offensive material in some of the posts (but Im not one to judge others whatsoever). Since 2010 this blog is now an archive for upcoming movies or video games. For more current affairs, do check out my Facebook page, thanks.
Monday, January 30, 2012
Saturday, January 28, 2012
Dinosaurs Live highlight 28: Triceratops
Triceratops is a genus of herbivorous ceratopsid dinosaur which lived during the late Maastrichtian stage of the Late Cretaceous Period, around 68 to 65 million years ago (Mya) in what is now North America. It was one of the last dinosaur genera to appear before the great Cretaceous–Paleogene extinction event. The term Triceratops, which literally means "three-horned face," is derived from the Greek τρί- (tri-) meaning "three", κέρας (kéras) meaning "horn", and ὤψ (ops) meaning "face".
Bearing a large bony frill and three horns on its large four-legged body, and conjuring similarities with the modern rhinoceros, Triceratops is one of the most recognizable of all dinosaurs and the best known ceratopsid. It shared the landscape with and was preyed upon by the fearsome Tyrannosaurus, though it is less certain that the two did battle in the manner often depicted in traditional museum displays and popular images.
The exact placement of the Triceratops genus within the ceratopsid group has been debated by paleontologists. Two species, T. horridus and T. prorsus, are considered valid although many other species have been named. Recent research suggests that the contemporaneous Torosaurus, a ceratopsid long regarded as a separate genus, actually represents Triceratops in its mature form.
Triceratops has been documented by numerous remains collected since the genus was first described in 1889, including at least one complete individual skeleton. Paleontologist John Scannella observed: "It is hard to walk out into the Hell Creek Formation and not stumble upon a Triceratops weathering out of a hillside." Forty-seven complete or partial skulls were discovered in just that area during the decade 2000–2010. Specimens representing life stages from hatchling to adult have been found.
Description
The function of the frills and three distinctive facial horns has long inspired debate. Traditionally these have been viewed as defensive weapons against predators. More recent theories, noting the presence of blood vessels in the skull bones of ceratopsids, find it more probable that these features were primarily used in identification, courtship and dominance displays, much like the antlers and horns of modern reindeer, mountain goats, or rhinoceros beetles. The theory finds additional support if Torosaurus represents the mature form of Triceratops, as this would mean the frill also developed holes (fenestrae) as individuals reached maturity, rendering the structure more useful for display than defense.
Individual Triceratops are estimated to have reached about 7.9 to 9.0 m (26.0–29.5 ft) in length, 2.9 to 3.0 m (9.5–9.8 ft) in height, and 6.1–12.0 tonnes (13,000–26,000 lb) in weight. The most distinctive feature is their large skull, among the largest of all land animals. The largest known skull (specimen BYU 12183) is estimated to have been 2.5 metres (8.2 ft) in length when complete, and could reach almost a third of the length of the entire animal. It bore a single horn on the snout, above the nostrils, and a pair of horns approximately 1 m (3 ft) long, with one above each eye. To the rear of the skull was a relatively short, bony frill, adorned with epoccipitals in some specimens. Most other ceratopsids had large fenestrae in their frills, while those of Triceratops were noticeably solid.
Friday, January 27, 2012
Dinosaurs Live highlight 27: Stegosaurus
Stegosaurus (meaning "roof lizard" or "covered lizard" in reference to its bony plates) is a genus of armored stegosaurid dinosaur. They lived during the Late Jurassic period (Kimmeridgian to early Tithonian), some 155 to 150 million years ago in what is now western North America. In 2006, a specimen of Stegosaurus was announced from Portugal, showing that they were present in Europe as well. Due to its distinctive tail spikes and plates, Stegosaurus is one of the most recognizable dinosaurs. At least three species have been identified in the upper Morrison Formation and are known from the remains of about 80 individuals.
A large, heavily built, herbivorous quadruped, Stegosaurus had a distinctive and unusual posture, with a heavily rounded back, short forelimbs, head held low to the ground and a stiffened tail held high in the air. Its array of plates and spikes has been the subject of much speculation. The spikes were most likely used for defense, while the plates have also been proposed as a defensive mechanism, as well as having display and thermoregulatory functions. Stegosaurus had a relatively low brain-to-body mass ratio. It had a short neck and small head, meaning it most likely ate low-lying bushes and shrubs. It was the largest of all the stegosaurians (bigger than genera such as Kentrosaurus and Huayangosaurus) and, although roughly bus-sized, it nonetheless shared many anatomical features (including the tail spines and plates) with the other stegosaurian genera.
Description
Averaging around 9 meters (30 ft) long and 4 meters (14 ft) tall, the quadrupedal Stegosaurus is one of the most easily identifiable dinosaurs, due to the distinctive double row of kite-shaped plates rising vertically along its rounded back and the two pairs of long spikes extending horizontally near the end of its tail. Although a large animal, it was dwarfed by its contemporaries, the giant sauropods. Some form of armor appears to have been necessary, as it coexisted with large predatory theropod dinosaurs, such as the fearsome Allosaurus and Ceratosaurus.
The hind feet each had three short toes, while each forefoot had five toes; only the inner two toes had a blunt hoof. All four limbs were supported by pads behind the toes. The forelimbs were much shorter than the stocky hindlimbs, which resulted in an unusual posture. The tail appears to have been held well clear of the ground, while the head of Stegosaurus was positioned relatively low down, probably no higher than 1 meter (3.3 ft) above the ground.
The long and narrow skull was small in proportion to the body. It had a small antorbital fenestra, the hole between the nose and eye common to most archosaurs, including modern birds, though lost in extant crocodylians. The skull's low position suggests that Stegosaurus may have been a browser of low-growing vegetation. This interpretation is supported by the absence of front teeth and their replacement by a horny beak or rhamphotheca. Stegosaurian teeth were small, triangular and flat; wear facets show that they did grind their food. The inset placement in the jaws suggests that Stegosaurus had cheeks to keep food in their mouths while they chewed.
Despite the animal's overall size, the braincase of Stegosaurus was small, being no larger than that of a dog. A well-preserved Stegosaurus braincase allowed Othniel Charles Marsh to obtain in the 1880s a cast of the brain cavity or endocast of the animal, which gave an indication of the brain size. The endocast showed that the brain was indeed very small, maybe the smallest among the dinosaurs. The fact that an animal weighing over 4.5 metric tons (5 short tons) could have a brain of no more than 80 grams (2.8 oz) contributed to the popular old idea that dinosaurs were unintelligent, an idea now largely rejected.
Thursday, January 26, 2012
Dinosaurs Live highlight 26: Ornithomimus
Ornithomimus ("bird mimic") is a genus of ornithomimid dinosaur from the Late Cretaceous Period of what is now North America.
In 1890 Ornithomimus velox was named by Othniel Charles Marsh on the basis of a foot and partial hand from the Maastrichtian Denver Formation. Another seventeen species have been named since. Most of these have subsequently been assigned to new genera or shown to be not directly related to Ornithomimus. The best material of species still considered part of the genus has been found in Canada, representing the earlier Edmontonian-age Ornithomimus edmontonicus Sternberg 1933, known from several skeletons. However, on some of these the new genus Dromiceiomimus including Dromiceiomimus brevitertius (Parks 1926) has been based, causing taxonomic problems of priority and identity that are still unresolved.
Ornithomimus was a relatively small swift bipedal animal, equipped with a small toothless beaked head, that may indicate an omnivorous diet.
Description
Like other ornithomimids, Ornithomimus is characterized by a foot with three weight-bearing toes, long slender arms and a long neck with a birdlike, elongated, toothless, beaked skull. It was bipedal and superficially resembled an ostrich, except for its long tail. It would have been a swift runner. It had very long limbs, hollow bones, and a large brain and eyes. The brains of ornithomimids were large for dinosaurs, but this may not necessarily be a sign of greater intelligence; some paleontologists think that the enlarged portions of the brain were dedicated to kinesthetic coordination. Their hands are remarkably sloth-like in appearance, which led Henry Fairfield Osborn to suggest that they were used to hook branches during feeding.
Ornithomimus differs from other ornithomimids, such as Struthiomimus, in having a short back, long slender forearms, very slender, straight hand and foot claws and in having metacarpals and fingers of similar lengths.
The three Ornithomimus species today seen as possibly valid, differ rather in size. In 2010 Gregory S. Paul estimated the length of O. edmontonicus at 3.8 metres, its weight at 170 kilograms (370 lb). One of its specimens, CMN 12228, preserves a femur (thigh bone) 46.8 centimetres (18.4 in) long. O. sedens was by Paul estimated at 4.8 metres and 350 kilograms (770 lb). O. velox, the type species of Ornithomimus, is based on material of a much smaller animal. Whereas the holotype of O. edmontonicus, CMN 8632, preserves a second metacarpal eighty-four millimetres long, the same element with O. velox measures only fifty-three millimetres.
Paleobiology
The diet of Ornithomimus is still debated. As theropods, ornithomimids might have been carnivorous but their body shape would also have been suited for a partly or largely herbivorous lifestyle. Suggested food includes insects, crustaceans, fruit, leaves, branches, eggs, and the meat of lizards and small mammals.
Ornithomimus had legs that seem clearly suited for rapid locomotion, with the tibia about 20% longer than the femur. The large eye sockets suggest a keen visual sense, and also suggest the possibility that they were nocturnal.
Wednesday, January 25, 2012
Dinosaurs Live highlight 25: Iguanodon
Iguanodon (meaning "iguana-tooth") is a genus of ornithopod dinosaur that lived roughly halfway between the first of the swift bipedal hypsilophodontids and the ornithopods' culmination in the duck-billed dinosaurs. Many species of Iguanodon have been named, dating from the Kimmeridgian age of the Late Jurassic Period to the Cenomanian age of the Late Cretaceous Period from Asia, Europe, and North America. However, research in the first decade of the 21st century suggests that there is only one well-substantiated species: I. bernissartensis, that lived from the late Barremian to the earliest Aptian ages (Early Cretaceous) in Belgium, between about 126 and 125 million years ago. Iguanodon's most distinctive features were its large thumb spikes, which were possibly used for defence against predators, combined with long prehensile fifth fingers able to forage for food.
Named in 1825 by English geologist Gideon Mantell, Iguanodon was the second dinosaur formally named, after Megalosaurus. Together with Megalosaurus and Hylaeosaurus, it was one of the three genera originally used to define Dinosauria. A large, bulky herbivore, Iguanodon is a member of Iguanodontia, along with the duck-billed hadrosaurs. The taxonomy of this genus continues to be a topic of study as new species are named or long-standing ones reassigned to other genera.
Scientific understanding of Iguanodon has evolved over time as new information has been obtained from the fossils. The numerous specimens of this genus, including nearly complete skeletons from two well-known bonebeds, have allowed researchers to make informed hypotheses regarding many aspects of the living animal, including feeding, movement, and social behaviour. As one of the first scientifically well-known dinosaurs, Iguanodon has occupied a small but notable place in the public's perception of dinosaurs, its artistic representation changing significantly in response to new interpretations of its remains.
Description
Iguanodon was a bulky herbivore that could shift from bipedality to quadrupedality. The best-known species, I. bernissartensis, is estimated to have weighed about 3 tonnes (3.5 tons) on average, and measured about 10 metres long (33 ft) as an adult, with some specimens possibly as long as 13 metres (43 ft). This genus had a large, tall but narrow skull, with a toothless beak probably covered with keratin, and teeth like those of an iguana, but much larger and more closely packed.
The arms were long (up to 75% the length of the legs in I. bernissartensis) and robust,[4] with rather inflexible hands built so that the three central fingers could bear weight. The thumbs were conical spikes that stuck out away from the three main digits. In early restorations, the spike was placed on the animal's nose. Later fossils revealed the true nature of the thumb spikes, although their exact function is still debated. They could have been used for defense, or for foraging for food. The little finger was elongated and dextrous, and could have been used to manipulate objects. The legs were powerful, but not built for running, and each foot had three toes. The backbone and tail were supported and stiffened by ossified tendons, which were tendons that turned to bone during life (these rod-like bones are usually omitted from skeletal mounts and drawings). Overall, in body structure, it was not too dissimilar from its later relatives, the hadrosaurids.
Tuesday, January 24, 2012
Dinosaurs Live highlight 24: Nanotyrannus
Nanotyrannus ("dwarf tyrant") is a genus of tyrannosaurid dinosaur, known only from two juvenile specimens, which may in fact represent juvenile specimens of the contemporary species Tyrannosaurus rex.
Description: Differences from the T-Rex
The primary differences that some scientists have used to distinguish Nanotyrannus lancensis from Tyrannosaurus rex primarily concern the number of teeth. Nanotyrannus had more teeth in its upper and lower jaws than an adult Tyrannosaurus. N. lancensis had 14-15 teeth in each side of the upper jaw (maxilla) and 16 teeth in each side of the lower jaw (dentary). T. rex, on the other hand, had 11-12 tooth positions in the upper jaw and 11-14 in the lower. The exact implications of this difference in tooth count has been controversial. In his 1999 study of tyrannosaurid growth patterns, Carr showed that in Gorgosaurus libratus, the number of teeth decreased as the animal grew, and he used this data to support the hypothesis that N. lancensis is simply a juvenile T. rex. The team of scientists who studied growth in the related Tarbosaurus bataar found little to no decrease in tooth count as that species grew, even though they had juvenile specimens much younger than the Nanotyrannus specimens. These researchers also noted, however, that in both Tyrannosaurus and Gorgosaurus, there were significant differences in tooth count between individuals of the same age group, and that tooth count may vary on an individual basis not related to growth.
Another difference cited by those who support the validity of N. lancensis is the presence of a small foramen, or pit, in the quadratojugal, a bone in the back corner of the skull. Both the holotype and the "Jane" specimen have this feature, suggesting it is not a deformity, and it is not known in any adult tyrannosaurid specimens. It is possible that this is again an individual variant, or that it was a feature lost as the animals grew, though studies of other juvenile tyrannosaurids do not show an equivalent feature.
Monday, January 23, 2012
Dinosaurs Live highlight 23: Utahraptor
Utahraptor (meaning "Utah's predator" or "Utah thief") is a genus of theropod dinosaurs, including the largest known members of the family Dromaeosauridae. Fossil specimens date to the upper Barremian stage of the early Cretaceous period (in rock strata dated to 126 ± 2.5 million years ago). It contains a single species, Utahraptor ostrommaysorum.
Description
The holotype specimen of Utahraptor is fragmentary, consisting of skull fragments, a tibia, claws and some caudal (tail) vertebra. These few elements suggest an animal about twice the size of Deinonychus. Like other dromaeosaurids, Utahraptor had large curved claws on their second toes. One claw specimen is preserved at 22 centimetres (8.7 in) in length and is thought to reach 24 centimetres (9.4 in) restored.
The largest described U. ostrommaysorum specimens are estimated to have reached up to 7 m (23 ft) long and somewhat less than 500 kg (1,100 lb) in weight, comparable to a grizzly bear in size. Some undescribed specimens in the BYU collections may have reached up to 11 m (36 ft) long, though these await more detailed study.
It is thought that Utahraptor may be closely related to the smaller Dromaeosaurus and the giant Mongolian dromaeosaurid genus Achillobator.
Although feathers have never been found in association with Utahraptor specimens, there is strong phylogenetic evidence suggesting that all dromaeosaurids possessed them. This evidence comes from phylogenetic bracketing, which allows paleontologists to infer traits that exist in a clade based on the existence of that trait in a more basal form. The genus Microraptor is one of the oldest known dromaeosaurids, and is phylogenetically more primitive than Utahraptor. Since Microraptor possessed feathers, it is reasonable to assume that this trait was present in all of Dromaeosauridae. Feathers were very unlikely to have evolved more than once in dromaeosaurids, so assuming that Utahraptor lacked feathers would require positive evidence that they did not have them. So far, there is nothing to suggest that feathers were lost in larger, more derived species of dromaeosaurs.
Sunday, January 22, 2012
Dinosaurs Live highlight 22: Pachycephalosaurus
Pachycephalosaurus (meaning "thick headed lizard," from Greek pachys-/παχυς- "thick", kephale/κεφαλη "head" and sauros/σαυρος "lizard") is a genus of pachycephalosaurid dinosaur. It lived during the Late Cretaceous Period (Maastrichtian stage) of what is now North America. Remains have been excavated in Montana, South Dakota, and Wyoming. It was an herbivorous or omnivorous creature which is only known from a single skull and a few extremely thick skull roofs. This dinosaur is monotypic, meaning the type species, P. wyomingensis, is the only known species. Pachycephalosaurus was one of the last non-avian dinosaurs before the K–T extinction event. Another dinosaur, Tylosteus of western North America, has been synonymized with Pachycephalosaurus.
Like other pachycephalosaurids, Pachycephalosaurus was a bipedal omnivore with an extremely thick skull roof. It possessed long hindlimbs and small forelimbs. Pachycephalosaurus is the largest known pachycephalosaur.
The thick skull domes of Pachycephalosaurus and related genera gave rise to the hypothesis that pachycephalosaurs used their skulls in intraspecific combat. This hypothesis has been disputed in recent years.
Description
The anatomy of Pachycephalosaurus is poorly known, as only skull remains have been described. Pachycephalosaurus is famous for having a large, bony dome atop its skull, up to 25 cm (10 in) thick, which safely cushioned its tiny brain. The dome's rear aspect was edged with bony knobs and short bony spikes projected upwards from the snout. The spikes were probably blunt, not sharp.
The skull was short, and possessed large, rounded eye sockets that faced forward, suggesting that the animal had good vision and was capable of binocular vision. Pachycephalosaurus had a small muzzle which ended in a pointed beak. The teeth were tiny, with leaf-shaped crowns. The head was supported by an "S"- or "U"-shaped neck.
Pachycephalosaurus was probably bipedal and was the largest of the pachycephalosaurid (bone-headed) dinosaurs. It has been estimated that Pachycephalosaurus was around 4.5 metres (15 ft) long and weighed 450 kilograms (990 lb). Based on other pachycephalosaurids, it probably had a fairly short, thick neck, short fore limbs, a bulky body, long hind legs and a heavy tail, which was likely held rigid by ossified tendons.
Classification
Pachycephalosaurus gives its name to the Pachycephalosauria, a clade of herbivorous ornithischian ("bird hipped") dinosaurs which lived during the Late Cretaceous Period in North America and Asia. Despite their bipedal stance, they were likely more closely related to the ceratopsians than the ornithopods.
Saturday, January 21, 2012
Dinosaurs Live highlight 21: Protoceratops
Protoceratops (from Greek proto-/πρωτο- "first", cerat-/κερατ- "horn" and -ops/-ωψ "face", meaning "First Horned Face") is a genus of sheep-sized (1.5 to 2 m long) herbivorous ceratopsian dinosaur, from the Upper Cretaceous Period (Campanian stage) of what is now Mongolia. It was a member of the Protoceratopsidae, a group of early horned dinosaurs. Unlike later ceratopsians, however, it was a much smaller creature that lacked well-developed horns and retained some primitive traits not seen in later genera.
Protoceratops had a large neck frill, which may have served to protect the neck, to anchor jaw muscles, to impress other members of the species, or combinations of these functions. Described by Walter Granger and W.K. Gregory in 1923, Protoceratops was initially believed to be an ancestor of the North American ceratopsians. Researchers currently distinguish two species of Protoceratops (P. andrewsi and P. hellenikorhinus), based in part by their respective sizes.
Description
Protoceratops was a quadrupedal dinosaur that was partially characterized by its distinctive neck frill at the back of its skull. The frill itself contained two large parietal fenestra (holes in the frill), while its cheeks had large jugal bones. The exact size and shape of the neck frill varied by individual; some specimens had short, compact frills, while others had frills nearly half the length of the skull. The frill consists mostly of the parietal bone and partially of the squamosal. Some researchers, including Peter Dodson attribute the different sizes and shapes of these bones to sexual dimorphism, as well as the age of the specimen, at the time of death.
Protoceratops was approximately 1.8 meters (6 ft) in length and 0.6 meters (2 ft) high at the shoulder. A fully grown adult would have weighed less than 400 pounds (180 kg). The large numbers of specimens found in high concentration suggest that Protoceratops lived in herds.
Protoceratops was a relatively small dinosaur with a proportionately large skull. Despite being herbivorous, Protoceratops appears to have had muscular jaws capable of a powerful bite. These jaws were packed with dozens of teeth, well suited for chewing tough vegetation. The skull consisted of a massive frontal beak, and four pairs of fenestrae (skull openings). The foremost hole, the naris, was considerably smaller than the nostrils seen in later genera. Protoceratops had large orbits (the holes for its eyes), which measured around 50 millimeters in diameter. Behind the eye was a slightly smaller fenestra, known as the "infratemporal fenestra."
Daily activity patterns
The large eyes of Protoceratops has been suggested as evidence for a nocturnal lifestyle. However, subsequent comparisons between the scleral rings of Protoceratops and modern birds and reptiles have indicated a more cathemeral lifestyle, being active throughout the day during short intervals. This suggests that the fight between Protoceratops and the primarily nocturnal Velociraptor indicated by the fighting specimens may have occurred at twilight or under low-light conditions.
Friday, January 20, 2012
Dinosaurs Live highlight 20: Omeisaurus
Omeisaurus (meaning "Omei lizard") is a genus of sauropod dinosaur from the Middle Jurassic Period (Bathonian-Callovian stage) of what is now China. Its name comes from Mount Emei, where it was discovered in the lower Shaximiao Formation of Sichuan Province.
Like other sauropods, Omeisaurus was herbivorous and large. It measured 10 to 15.2 metres (30 to 50 ft) long, 4 metres (12 ft) high and weighed 4 tons.
Omeisaurus was first described in 1939. It was named after the sacred mountain Omeishan, which is were the first fossil example of Omeisaurus was found. Most skeletons of Omeisaurus were found in the 1970s and 1980s, during the great “Chinese Dinosaur rush”. There have been six species of Omeisaurus named so far: O. junghsiensis, O. changshouensis, O. fuxiensis, O. tianfuensis, O. luoquanensis, and O. maoianus. All of these but the last were named after the locations where they were found. O. fuxiensis was the smallest species, measuring around 35 feet (11 m) long. O. tianfuensis had the longest neck of the genus, around 30 feet (9.1 m) long. The only dinosaur with a longer neck was Mamenchisaurus. A club tail fossil discovered in the same bone bed as the Omeisaurus fossils was thought to belong to this genus, but is now believed to belong to a large specimen of Shunosaurus.
Mounted skeletons of Omeisaurus are on display at the Zigong Dinosaur Museum in Zigong, Sichuan Province and at Beipei Museum, near Chongqing, both in China.
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