Mosasaurus was among the last mosasaur genera, and among the largest. The skull was more robustly built than other mosasaurs, as the mandibles articulated very tightly with the skull. It had a deep, barrel-shaped body, and with its fairly large eyes, poor binocular vision, and poorly developed olfactory bulbs, experts believe that Mosasaurus lived near the ocean surface, where it preyed on fish, turtles, ammonites, and possibly smaller mosasaurs. The animal remained near the surface and although it was able to dive, it evidentially did not venture into deeper waters.

The skull of Mosasaurus tapered off into a short, conical process, and the jaws were armed with massive, sharp, conical teeth. Their paddle-like limbs had five digits in front and four in back. The trunk terminated in a strong tail which, together with serpentine undulation of the whole body, contributed far more to the animal's locomotion that did the limbs.

Because of its robust skull and tightly articulating jaws, Mosasaurus was unable to swallow prey-items whole in the manner of earlier mosasaurs, such as Tylosaurus[citation needed]. Instead, with the aid of its curved, knife-like teeth, Mosasaurus was able to tear its prey into more manageable pieces that could be more easily swallowed.

Mosasaurus ("lizard of the Meuse River") was a genus of mosasaur, a carnivorous, aquatic lizard, somewhat resembling a flippered crocodile, with elongated heavy jaws. The genus lived in the Maastrichtian age of the Cretaceous period (Mesozoic era), around 70-65 millions years ago in the area of modern Western Europe.

As with most mosasaurs, their legs and feet are modified into hydrofoil-like flippers, with the forelimbs larger than the hindlimbs. Like its American relatives Tylosaurus and Hainosaurus, Mosasaurus reached lengths of about 17 meters.


Allosaurus fragilis had an average length of 8.5 meters (28 ft), with the largest definitive Allosaurus specimen (AMNH 680) estimated at 9.7 meters long (32 ft), and an estimated weight of 2.3 metric tons (2.5 short tons).Allosaurus was a typical large theropod, having a massive skull on a short neck, a long tail and reduced forelimbs. As with dinosaurs in general, weight estimates are debatable, and since 1980 have ranged between 1500 kilograms (3300 lb), 1000 to 4000 kilograms (2200 to 8800 lb), and 1010 kilograms (2230 lb) for modal adult weight (not maximum).

Several gigantic specimens have been attributed to Allosaurus, but may in fact belong to other genera. The closely related genus Saurophaganax (OMNH 1708) reached perhaps 10.9 meters (36 ft) in length, and its single species has sometimes been included in the genus Allosaurus as Allosaurus maximus, though recent studies support it as a separate genus. Another potential specimen of Allosaurus, once assigned to the genus Epanterias (AMNH 5767), may have measured 12.1 meters in length (40 ft). A more recent discovery is a partial skeleton from the Peterson Quarry in Morrison rocks of New Mexico; this large allosaurid may be another individual of Saurophaganx.


Skull of the Allosaurus fragilis skeleton mounted in the lobby of the San Diego Natural History Museum. The skull and teeth of Allosaurus were modestly proportioned for a theropod of its size. Paleontologist Gregory S. Paul gives a length of 845 millimeters (33.3 in) for a skull belonging to an individual he estimates at 7.9 meters long (26 ft). Each premaxilla (the bones that formed the tip of the snout), held five teeth with D-shaped cross-sections, and each maxilla (the main tooth-bearing bones in the upper jaw) had between fourteen and seventeen teeth; the number of teeth does not exactly correspond to the size of the bone. Each dentary (the tooth-bearing bone of the lower jaw) had between fourteen and seventeen teeth, with an average count of sixteen.

The skull had a pair of horns above and in front of the eyes. These horns were composed of extensions of the lacrimal bones,and varied in shape and size. There were also lower paired ridges running along the top edges of the nasal bones that led into the horns. The horns were probably covered in a keratin sheath and may have had a variety of functions, including acting as sunshades for the eye, being used for display, and being used in combat against other members of the same species (although they were fragile). There was a ridge along the back of the skull roof for muscle attachment, as is also seen in tyrannosaurids.

Allosaurus is a genus of large theropod dinosaur that lived 155 to 145 million years ago, in the late Jurassic period (Kimmeridgian to Tithonian). The name Allosaurus means "different lizard" and is derived from the Greek αλλος/allos ("different, strange") and σαυρος/sauros ("lizard"). The first remains that can definitely be ascribed to this genus were described in 1877 by Othniel Charles Marsh. As one of the first well-known theropod dinosaurs, it has long attracted attention outside of paleontological circles, and has been a lead dinosaur in several films and documentaries.

Allosaurus was a large bipedal predator with a large skull, equipped with dozens of large, sharp teeth. The preys of the Allosaurus were the Diplodocus or Stegosaurus.


Miacis is an extinct that appeared in the late Paleocene (ca. 60-55 million years ago) and are mammals of the family Miacidae. They are representative of the group of early carnivores that were the ancestors of the modern Order Carnivora, although only the species Miacis cognitus is a true carnivoran. Thus, Miacis may be considered the genus of carnivorous mammals that gave rise to all modern Carnivora (dogs and cats).

Miacis was about the size of a weasel (~30 cm), and lived on the North American and European continents. They retained some of the primitive characteristics that were present in the Creodonts, the sister order of Carnivora, such as low skulls, long slender bodies, long tails, and short legs. It retained the same number of teeth, 44, although some reductions in this number were apparently in progress and some of the teeth were reduced in size.

The hind limbs were longer than the forelimbs, the pelvis was very doglike in form and structure, and some specialized traits were present in the vertebrae. It had retractable claws, agile joints for climbing, and binocular vision. Miacis and related forms had brains that were relatively larger than those of the creodonts, and the increase in brain size as compared with body size probably reflects an increase in intelligence.

Like many other early carnivorans, it was well suited for an arboreal climbing lifestyle with needle sharp claws, and had limbs and joints that resemble those of modern carnivorans. Miacis was probably a very agile forest dweller that preyed upon smaller animals, such as small mammals, reptiles, and birds, and might have also have eaten eggs and fruits.


The Smilodon are among the largest felids, the heaviest specimens of this massively built carnivore may have exceeded 400 kg (880 lb).

A Smilodon had a short tail, powerful legs, muscular neck and long canines. Despite being around the same size as a tiger or lion, Smilodon was more robustly built, comparable to a bear.
It shown to scale to demonstrate the compact muscular buildA fully-grown Smilodon weighed approximately 55 to 360 kg (120 to 790 lb), depending on species.

Smilodon had relatively shorter and more massive limbs than other felines. It had well developed flexors and extensors in its forepaws,[citation needed] which enabled it to pull down large prey. The back limbs had powerfully built adductor muscles which might have helped the cat's stability when wrestling with prey. Its claws were retractable.

Teeth and jaws

They are the longest canines of the saber-toothed cats at about 28 cm (11 in) long in the largest species Smilodon populator. They were probably built more for stabbing than slashing. Despite being more powerfully built than other large cats, Smilodon actually had a weaker bite. Modern big cats have more pronounced zygomatic arches, while Smilodon had smaller zygomatic arches which restricted the thickness and therefore power of the temporalis muscles, and thus reduced Smilodon’s bite force. Analysis of its narrow jaws indicates that it could produce a bite only a third as strong as that of a lion.There seems to a be a general rule that the saber-toothed cats with the largest canines had proportionally weaker bites. However, analyses of canine bending strength (the ability of the canine teeth to resist bending forces without breaking) and bite forces indicate that saber-toothed cats' teeth were stronger relative to the bite force than those of modern "big cats". In addition, Smilodon could open its jaws 120 degrees, whereas the lion can only open its jaws to 65 degrees.

Smilodon probably preyed on a wide variety of large game including bison, Megatherium, Aurochs, deer, American camels, horses and . As it is known for the saber-toothed cat Homotherium, Smilodon might have killed also juvenile mastodons and mammoths.

Smilodon called sabre-toothed cat or sabre-toothed tiger, is an extinct genus of the subfamily machairodontine saber-toothed cats endemic to North America and South America living from the Early Pleistocene through Lujanian stage of the Pleistocene epoch (1.8 mya—10,000 years ago), existing for approximately 1.790 milion years.


Velociraptor was a prehistoric animal measuring up to 2.07 m (6.8 ft) long, 0.5 m (1.6 ft) high at the hip, and weighing up to 15 kg (33 lb). The skull, which grew up to 25 cm (9.8 in) long, was uniquely up-curved, concave on the upper surface and convex on the lower. The jaws were lined with 26–28 widely spaced teeth on each side, each more strongly serrated on the back edge than the front—possibly an adaptation that improved its ability to catch and hold fast-moving prey.

Velociraptor, like other dromaeosaurids, had a large manus ('hand') with three strongly curved claws, which were similar in construction and flexibility to the wing bones of modern birds. The second digit was the longest of the three digits present, while the first was shortest. The structure of the carpal (wrist) bones prevented pronation of the wrist and forced the 'hands' to be held with the palmar surface facing inwards (medially), not downwards. However, whereas most theropods had feet with three digits contacting the ground, dromaeosaurids like Velociraptor walked on only their third and fourth digits. The second digit, for which Velociraptor is most famous, was highly modified and held retracted off of the ground. It bore a relatively large, sickle-shaped claw, typical of dromaeosaurid and troodontid dinosaurs. This enlarged claw, which could be over 6.5 cm (2.6 in) long around its outer edge, was most likely a predatory device used to tear into prey, possibly delivering a fatal blow.

Velociraptor (meaning 'swift seizer') is a genus of dromaeosaurid theropod dinosaur that existed approximately 75 to 71 mya (million years ago) during the later part of the Cretaceous Period. Only two species are currently recognized, although others have been assigned in the past. The type species is V. mongoliensis; fossils of this species have been discovered in both Inner and Outer Mongolia in central Asia. A second species, V. osmolskae, was named in 2008 for skull material from Inner Mongolia.

In 2007, paleontologists reported the discovery of quill knobs on a well-preserved Velociraptor mongoliensis forearm from Mongolia, confirming the presence of feathers in this species


Meganeura monyi was a prehistoric insect resembling and related to the present-day dragonfly of the Carboniferous period (300 million years ago), . With a wingspan of more than 75 cm (2.5 ft) wide, it was the largest known flying insect species ever to appear on Earth. (The Permian Meganeuropsis permiana is another contender). It was predatory, feeding on other insects and even small amphibians.

Controversy has prevailed as to how insects of the Carboniferous period were able to grow so large. The way oxygen is diffused through the insect's body via its tracheal breathing system puts an upper limit on body size, which prehistoric insects seem to have well exceeded. It was originally proposed (Harlé & Harlé, 1911) that Meganeura was only able to fly because the atmosphere at that time contained more oxygen than the present 20%. This theory was dismissed by fellow scientists, but has found approval more recently through further study into the relationship between gigantism and oxygen availability. If this theory is correct, these insect giants would have been perilously susceptible to falling oxygen levels and certainly could not survive in our modern atmosphere.

However, more recent research indicates that insects really do breathe, with "rapid cycles of tracheal compression and expansion". If correct, then there is no need to postulate an atmosphere with higher oxygen partial pressure.
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