Temporal range: Late Cretaceous, 70 Ma
|Reconstructed skeleton, Royal Ontario Museum, Toronto, Canada|
Sampson et al., 2001
|Species:||† M. knopfleri|
Sampson et al., 2001
Masiakasaurus is a genus of small predatory theropod dinosaurs from the Late Cretaceous of Madagascar. In Malagasy, masiaka means "vicious"; thus, the genus name means "vicious lizard". The type species, Masiakasaurus knopfleri, was named after the musician Mark Knopfler, whose music inspired the expedition crew. It was named in 2001 by Scott D. Sampson, Matthew Carrano, and Catherine A. Forster. Unlike most theropods, the front teeth of M. knopfleri projected forward instead of straight down. This unique dentition suggests that they had a specialized diet, perhaps including fish and other small prey. Other bones of the skeleton indicate that Masiakasaurus were bipedal, with much shorter forelimbs than hindlimbs. M. knopfleri reached an estimated adult body length of around 2 metres (6 ft 7 in).
Masiakasaurus lived around 70 million years ago, along with animals such as Majungasaurus, Rapetosaurus, and Rahonavis. Masiakasaurus was a member of the group Noasauridae, small predatory ceratosaurs found primarily in South America.
Masiakasaurus were small-bodied ceratosaurs that grew up to around 1.8 to 2 metres (5.9 to 6.6 ft) in length. The most distinctive characteristic of Masiakasaurus is the forward-projecting, or procumbent, front teeth. The teeth are heterodont, meaning that they have different shapes along the jaw. The first four dentary teeth of the lower jaw project forward, with the first tooth angled only 10° from horizontal. These teeth are long and spoon-shaped with hooked edges. They have carinae, or sharp edges, that are weakly serrated. Serrations are more evident in the posterior teeth, which are also recurved and laterally compressed. The margin of the dentary curves downward so that the tooth sockets of the front teeth are directed forward. The front teeth of the upper jaw are also procumbent, and the margin of the premaxilla curves slightly upward to direct them outward.
Unlike the skulls of abelisaurids, which are very deep, the skull of Masiakasaurus is long and low. The lacrimal and postorbital bones around the eye are textured with bumpy projections. Not including the highly modified jaws and teeth, the skull of Masiakasaurus possesses many general ceratosaurian characteristics. Overall, its morphology is intermediate between abelisaurids and more basal ceratosaurs.
The neck is relatively narrow in comparison to abelisaurids and bear stout neck ribs. While many theropods have s-shaped necks, the ribs would make the neck rather stiff in Masiakasaurus, and the back of the neck is positioned almost horizontally, giving it only a slighter curve. Like those of other abelisauroids, the vertebrae are heavily pneumaticized, or hollowed, and have relatively short neural spines. Pneumaticity is limited to the neck and foremost back vertebrae, however. Pneumatic cavities are also present in the braincase.
The scapulocoracoid, a bone that makes up the pectoral girdle, is large and broad. While abelisaurids have arms that are extremely reduced in size, Masiakasaurus and other noasaurids had longer forelimbs. The humerus is slender and the bones of the hand are relatively short. The related genus Noasaurus has a raptorial ungual which was originally interpreted as a sickle-like claw on the foot, but has more recently been considered a claw of the hand. The penultimate phalanx, a finger bone that immediately precedes the raptorial ungual in Noasaurus, is also known in Masiakasaurus and has a similar appearance. The enlarged ungual, however, is unknown in Masiakasaurus. The hand bore three large fingers with stout - but not particularly sharp - claws, and a highly reduced fourth finger.
Remains of Masiakasaurus have been found in the Late Cretaceous Maevarano Formation in northwestern Madagascar and were first described in the journal Nature in 2001. Fragmentary bones comprising around 40% of the skeleton were collected near the village of Berivotra. Several parts of the skull, including the distinctive teeth, were found. The humerus, pubis, hind limbs, and several vertebrae were also collected.
In 2011, additional specimens of Masiakasaurus were described. The braincase, premaxilla, facial bones, ribcage, portions of the hands and pectoral girdle, and much of the cervical and dorsal vertebral column were described for the first time. The discovery of this new material clarified many aspects of noasaurid anatomy and made the genus among the best known dinosaurs. The new finds did however not allow for a detailed study of its evolutionary relationships among ceratosaurs. With the new material, around 65% of the skeleton is currently known.
In its initial 2001 description, Masiakasaurus was classified as a basal abelisauroid related to Laevisuchus and Noasaurus, two poorly known genera named in 1933 and 1980, respectively. In the following year, Carrano et al. (2002) placed Masiakasaurus along with Laevisuchus and Noasaurus in the family Noasauridae. They conducted a phylogenetic analysis of abelisauroids using characteristics from Masiakasaurus. Below is a cladogram from an updated version of their analysis showing the phylogenetic placement of Masiakasaurus.
Carrano et al. (2002) distinguished two forms of Masiakasaurus, a robust form and a gracile form. The robust morph includes specimens with thicker bones and more pronounced projections for the attachment of ligaments and muscles. The gracile form includes specimens that are more slender and have less pronounced muscle attachments. It also has unfused tibiae, unlike the fused tibiae of the robust form. These two varieties may be an indication of sexual dimorphism in Masiakasaurus, but they may also represent two distinct populations.
One specimen of Masiakasaurus, a right scapulocoracoid, bears holes that may be puncture marks from predation or scavenging. Majungasaurus, a large abelisaurid from the Maevarano Formation, may have preyed upon Masiakasaurus. The holes may also have been the result of an infection.
The procument front teeth of Masiakasaurus were likely an adaptation for grasping small prey. They would have been unsuitable for tearing larger food apart. In the front of the jaws, carinae are restricted to the base of the teeth and would not have been used to tear prey. The back teeth, however, share the same general characteristics as those of most other theropods, suggesting that they served a similar function in Masiakasaurus such as cutting and slicing.
Several feeding behaviors have been proposed for Masiakasaurus on the basis of its unusual dentition. Because the front teeth would have been well suited for grasping, Masiakasaurus may have consumed small vertebrates, invertebrates, and possibly even fruits. It may also have been piscivorous, catching fish with the ends of its jaws and cutting and tearing them with its back teeth. Another feeding method that has been proposed for Masiakosaurus would be as a fossorial predator, hunting burrowing animals much like the Ethopian Wolf due to the fact that it has many features in common with other fossorial predators and that fish are relatively rare in the semiarid environment of Late Cretaceous Madagascar.
In 2013, Lee and O'Connor observed that Masiakasaurus would be a good subject for an analysis of theropod growth, considering that there is an abundance of fossil material to examine from a broad range of ontogenetic stages. The study showed that Masiakasaurus grew determinately, and reached full maturity at a small body size. Competing theories that Masiakasaurus specimens represent the juvenile form of a larger-bodied theropod were not supported by the data. Masiakasaurus took 8 to 10 years to grow the size of a large dog. This indicates a rate of growth that is 40% slower than that of comparably sized non-avian theropods, a finding that is supported by the unusual prominence of parallel-fibered bone which is known to be associated with relatively slow growth. However, individuals in this genus grew 40% faster than crocodylians. Lee and O'Connor noted that the evolution of slow growth gave this dinosaur the advantage of minimizing the nutritional investment allocated toward structural growth while living in a semiarid and seasonally stressful environment.
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