|Skeletal reconstruction of Spinosaurus aegyptiacus, National Geographic Museum, Washington, D.C.|
Spinosauridae (meaning "spined lizards") is a family of megalosauroidean theropod dinosaurs. The genus Spinosaurus, from which the family, subfamily, and tribe borrow their names, is the largest terrestrial predator known from the fossil record, and likely reached lengths of 15 m (49 ft). Most spinosaurids lived during the Cretaceous Period, with possible origins in the Late Jurassic, and fossils of them have been recovered worldwide, including in Africa, Europe, South America, Asia, and possibly Australia, although none have been formally named from the latter continent. Spinosaur remains have generally been attributed to the Early to Mid Cretaceous, with the exception of the Ostafrikasaurus from the Late Jurassic.
Spinosaurids were large bipedal carnivores with elongated, crocodile-like skulls lined with conical teeth bearing little to no serrations, and small crests on top of their heads. The teeth in the front end of their lower jaws fanned out into a spoon-shaped structure similar to a rosette, which gave the animal a characteristic look. Their shoulders were robust, prominent and bore stocky forelimbs with giant "hooked" claws on the first finger of their hands. Many genera had unusually tall neural spines on their vertebrae, which supported sails or humps of skin or fat tissue.
Direct fossil evidence and anatomical adaptations indicate that spinosaurids were at least partly piscivorous, with additional fossil finds indicating they also hunted pterosaurs and small to medium-sized dinosaurs. Osteological analyses have suggested a semiaquatic lifestyle for some members of this clade.
- 1 Description
- 2 History of discovery
- 3 Classification
- 4 Paleobiology
- 5 Paleoecology
- 6 Timeline of genera
- 7 Timeline of genera descriptions
- 8 References
- 9 External links
Although reliable size and weight estimates for most taxa are hindered by the lack of good material, all known spinosaurids were large animals. The smallest, Irritator, was between 6 and 8 meters in length and 1 tonne (1.1 short tons) in weight. While Ichthyovenator, Baryonyx, and Suchomimus ranged from 7.5 to 11 meters long, and weighing between 1 and 5.2 tonnes (1.2 and 5.7 short tons). Spinosaurus was the largest, capable of reaching lengths of around 15 meters (49 ft) and weighing around 6.4–7.2 tonnes (7.1–7.9 short tons). This consistency in large body size among spinosaurids could have evolved as a byproduct of their preference for semiaquatic lifestyles, as without the need to compete with other large theropods for food, they would have been able to grow to tremendous lengths.
Spinosaurid skull anatomy is similar in many respects to that of crocodilians. Spinosaurid skulls were long, low and narrow. As in other theropods, various fenestrae (openings) in the skull aided in reducing its weight. In spinosaurs however, the antorbital fenestrae were greatly reduced, akin to those of crocodilians. The tips of the premaxillae (frontmost snout bones) and dentaries (tooth bearing bones of the mandible) were expanded, forming what has been called a "terminal rosette" of enlarged teeth. Behind this expansion, the upper and lower jaws were notched. The maxillae (main upper jaw bones) were long and formed a low branch under the nostrils that connected to the rear of the premaxillae. Spinosaurid teeth were subconical, with an oval to circular cross section and either absent or very fine serrations. Typically, their teeth were either straight or only slightly recurved front to back, and bore a varying number of flutes (ridges) running lengthwise across their tooth crowns.
Lengthwise atop the skull ran a thin and shallow sagittal crest that was usually tallest near or above the eyes, either becoming shorter or disappearing entirely towards the front of the head. Spinosaurus's head crest was comb shaped and bore distinct vertical ridges, while those of Baryonyx and Suchomimus looked like small triangular bumps. Irritator's median crest stopped above the eyes in a bulbous, flattened shape. However, given that the upper surface of its holotype skull was damaged and the tip of its snout was missing, the complete shape of Irritator's crest is unknown. Angaturama (a possible synonym of Irritator) had an unusually tall crest on its premaxillae that nearly overhung the tip of the snout with a small protrusion.
The nostrils were set far back on the skull, at least behind the teeth of the premaxillae, instead of at the front of the snout as in most theropods. Those of Baryonyx and Suchomimus were large and started between the first and fourth maxillary teeth, while Spinosaurus's nostrils were far smaller and more retracted. Irritator's nostrils were positioned similarly to those of Baryonyx and Suchomimus, and were between those of Spinosaurus and Suchomimus in size. Spinosaurids had long secondary palates, bony and rugose structures on the roof of their mouths that are also found in extant crocodilians, but not in most theropod dinosaurs. Oxalaia had a particularly wrinkled and elaborate secondary palate, while most spinosaurs had smoother ones.
Spinosaurids had relatively large and well-built forelimbs, the radius (forearm bone) was stout and usually only half as long as the humerus (upper arm bone). Each manus (hand) wielded an enlarged, strongly recurved claw on the first digit (or "thumb"), and were otherwise typical of tetanurans, bearing three digits. The coracoids were hook shaped. The hindlimbs were somewhat short and mostly conventional of other megalosauroid theropods. Spinosaurus however, had a particularly small pelvic (hip) region and hindlimbs proportional to body size.
The upwards projecting neural spines of spinosaurid vertebrae were very tall, more so than in most theropods. When alive, these spines would have been covered in skin or fat tissue and formed a dorsal sail down the animal's back, a condition that has also been observed in some carcharodontosaurid and ornithopod dinosaurs. The eponymous neural spines of Spinosaurus were extremely long, some of the dorsal (back) vertebrae being over 1-metre (3 ft 3 in) tall. Suchomimus had a lower, ridge-like sail across the majority of its back, hip, and tail region. Baryonyx showed a reduced sail, with only few of the rearmost vertebrae being elongated. Ichthyovenator had a sinusoidal (wave-like) sail that split in two over the pelvic region, with the ends of some neural spines fanning out and bearing elongate, finger-like processes on their rear upper margins. One partial skeleton possibly refferable to Angaturama also had elongated neural spines on its hip region. The presence of a sail in fragmentary genera like Sigilmassasaurus is unknown.
History of discovery
The first spinosaurid fossil, a single conical tooth, was discovered circa 1820 by British paleontologist Gideon Mantell in the Wadhurst Clay Formation. In 1841 Sir Richard Owen mistakenly assigned it to a crocodilian he named Suchosaurus ("crocodile lizard"), a second species, S. girardi, was later named in 1897. However, the spinosaurid nature of Suchosaurus was not recognized until a 1998 redescription of Baryonyx.
The first fossils referred to a spinosaurid were discovered in 1912 at the Bahariya Formation in Egypt. Consisting of dorsal vertebrae, skull fragments, and teeth, these remains became the holotype specimen of the new genus and species Spinosaurus aegyptiacus in 1915, when they were described by German paleontologist Ernst Stromer. The dinosaur's name meant "egyptian spine lizard", in reference to the unusually long neural spines not seen previously in any other theropod. In April 1944, the holotype of S. aegyptiacus was destroyed during an allied bombing raid in World War II. In 1934, Stromer referred a partial skeleton also from the Bahariya Formation to a new species of Spinosaurus, this specimen has since been alternatively assigned to another African spinosaurid, Sigilmassasaurus.
In 1983, a relatively complete skeleton was excavated from the Smokejacks pit in Surrey, Engand. These remains were described by British paleontologists Alan J. Charig and Angela C. Milner in 1986 as the holotype of a new species, Baryonyx walkeri. After the discovery of Baryonyx, many new genera have since been described, the majority on very incomplete remains. However, other finds bear enough fossil material and distinct anatomical features to be assigned with confidence. Paul Sereno and colleagues described Suchomimus in 1998, a baryonychine from Niger on the basis of a partial skeleton found in 1997. Later in 2004, partial jaw bones were recovered from the Alcântara Formation, these were referred to a new genus of spinosaurine named Oxalaia in 2011 by Alexander Kellner.
The family Spinosauridae was named by Stromer in 1915 to include the single genus Spinosaurus. The clade was expanded as more close relatives of Spinosaurus were uncovered. The first cladistic definition of Spinosauridae was provided by Paul Sereno in 1998 (as "All spinosauroids closer to Spinosaurus than to Torvosaurus").
Traditionally, Spinosauridae is divided into two subfamilies: Spinosaurinae, which contains the genera Icthyovenator, Irritator, Oxalaia, Sigilmassasaurus and Spinosaurus, is marked by unserrated, straight teeth, and external nares which are further back on the skull than in Baryonychinae. And Baryonychinae, which contains the genera Baryonyx and Suchomimus, is marked by serrated, slightly curved teeth, smaller size, and more teeth in the lower jaw behind the terminal rosette than in spinosaurines. Others, such as Siamosaurus, may belong to either Baryonychinae or Spinosaurinae, but are too incompletely known to be assigned with confidence. Siamosaurus was classified as a spinosaurine in 2018, but the results are provisional and not entirely conclusive.
The subfamily Spinosaurinae was named by Sereno in 1998, and defined by Holtz and colleagues in 2004 as all taxa closer to Spinosaurus aegyptiacus than to Baryonyx walkeri. And the subfamily Baryonychinae was named by Charig & Milner in 1986. They erected both the subfamily and the family Baryonychinae for the newly discovered Baryonyx, before it was referred to the Spinosauridae. Their subfamily was defined by Holtz and colleagues in 2004, as the complementary clade of all taxa closer to Baryonyx walkeri than to Spinosaurus aegyptiacus. Examinations in 2017 by Marcos Sales and Cesar Schultz indicate that the South American spinosaurids Angaturama and Irritator were intermediate between Baronychinae and Spinosaurinae based on their craniodental features and cladistic analysis. This indicates that Baryonychinae may in fact be non-monophyletic. Their cladogram can be seen below.
The 2018 phylogenetic analysis by Arden and colleagues, which included many unnamed taxa, resolved Baryonychinae as monophyletic, and also coined the new term Spinosaurini for the clade of Sigilmassasaurus and Spinosaurus.
Diet and feeding
Spinosaurid teeth resemble those of crocodiles, which are used for piercing and holding prey. Therefore, teeth with small or no serrations, such as in spinosaurids, were not good for cutting or ripping into flesh but instead helped to ensure a strong grip on a struggling prey animal. Spinosaur jaws were likened by Vullo and colleagues to those of the pike conger eel, in what they hypothesized was convergent evolution for aquatic feeding. Both kinds of animals have some teeth in the end of the upper and lower jaws that are larger than the others and an area of the upper jaw with smaller teeth, creating a gap into which the enlarged teeth of the lower jaw fit, with the full structure called a terminal rosette.
In the past, spinosaurids have often been considered piscivores (fish-eaters) in the main, based on comparisons of their jaws with those of modern crocodilians. British paleontologist Emily J. Rayfield and colleagues, in 2007, conducted biomechanical studies on the skull of Baryonyx, which had a long, laterally compressed skull, comparing it to gharial (long, narrow, tubular) and alligator (flat and wide) skulls. They found that the structure of baryonychine jaws converged on that of gharials, in that the two taxa showed similar response patterns to stress from simulated feeding loads, and did so with and without the presence of a (simulated) secondary palate. The gharial, exemplar of a long, narrow, and tubular snout, is a fish specialist. However, this snout anatomy does not preclude other options for the spinosaurids. The gharial is the most extreme example and a fish specialist; Australian freshwater crocodiles (Crocodylus johnstoni), which have similarly shaped skulls to gharials, also specialize more on fish than sympatric, broad snouted crocodiles and are opportunistic feeders which eat all manner of small aquatic prey, including insects and crustaceans. Thus, spinosaurids' snouts correlate with piscivory; this is consistent with hypotheses of this diet for spinosaurids, in particular baryonychines, but it does not indicate that they were solely piscivorous.
Further study by Andrew R. Cuff and Rayfield in 2013 on the skulls of Spinosaurus and Baryonyx did not recover similarities in the skulls of Baryonyx and the gharial that the previous study did. Baryonyx had, in models where the size difference of the skulls was corrected for, greater resistance to torsion and dorsoventral bending than both Spinosaurus and the gharial, while both spinosaurids were inferior to the gharial, alligator, and slender-snouted crocodile in resisting torsion and medio-lateral bending. When the results from the modeling were not scaled according to size, then both spinosaurids performed better than all the crocodilians in resistance to bending and torsion, due to their larger size. Thus, Cuff and Rayfield suggest that the skulls are not efficiently built to deal well with relatively large, struggling prey, but that spinosaurids may overcome prey simply by their size advantage, and not skull build. Sues and colleagues studied the construction of the spinosaurid skull, and concluded that their mode of feeding was to use extremely quick, powerful strikes to seize small prey items using their jaws, whilst employing the powerful neck muscles in rapid up-and-down motion. Due to the narrow snout, vigorous side-to-side motion of the skull during prey capture is unlikely. Based the size and positions of their nostrils, Sales & Schultz in 2017 suggested that Spinosaurus possessed a greater reliance on its sense of smell and had a more piscivorous lifestyle than Irritator and baryonychines.
Direct fossil evidence shows that spinosaurids fed on fish as well as a variety of other small to medium-sized animals, including dinosaurs. Baryonyx was found with scales of the prehistoric fish Scheenstia in its body cavity, and these were abraded, hypothetically by gastric juices. Bones of a young Iguanodon, also abraded, were found alongside this specimen. If these represent Baryonyx’s meal, the animal was, whether in this case a hunter, or a scavenger, an eater of more diverse fare than fish. Moreover, there is a documented example of a spinosaurid having eaten a pterosaur, as one Irritator tooth was found embedded within the fossil vertebrae of an ornithocheirid pterosaur found in the Romualdo Formation of Brazil. This may represent a predation or a scavenging event. In the Sao Khua Formation of Thailand, isolated tooth crowns from Siamosaurus have been found in association with sauropod remains, indicating possible predation or scavenging.
A 2018 study by Hassler and colleagues of calcium isotopes in the teeth of North African theropods found that spinosaurids had a mixed diet of fish and herbivorous dinosaurs, whereas the other theropods examined (abelisaurids and carcharodontosaurids) mainly fed on herbivorous dinosaurs. This might indicate ecological partitioning between these theropods.
The use of the robust forelimbs and giant recurved claws of spinosaurs remains a debated topic. Charig and Milner speculated in 1986 that Baryonyx may have crouched by the riverbank and used its claws to gaff fish out of the water, similarly to grizzly bears. In 1987, British biologist Andrew Kitchener argued that with both its crocodile-like snout and enlarged claws, Baryonyx seemed to have too many adaptations for piscivory when one would have been enough. Kitchener instead postulated that Baryonyx more likely used its arms to scavenge the corpses of large dinosaurs, such as Iguanodon, by breaking into the carcass with the large claws, and subsequently probing for viscera with its long snout. In their 1997 article, Charig and Milner rejected this hypothesis, pointing out that in most cases, a carcass would have already been largely emptied out by its initial predators. Later research has also ruled out this sort of specialized scavenging. Charig and Milner further suggested that the robust forelimbs and giant thumb claws would have been Baryonyx's primary method of capturing, killing, and tearing apart large prey; whereas its long snout would have been used mostly for fishing. A 2005 study by Canadian paleontologist the François Therrien and colleagues agreed that spinosaur forelimbs were probably used for hunting larger prey items, given that their snouts could not resist the bending stress. In a 2017 review of the family, David Hone and Holtz considered a possible function in digging for water sources or hard to reach prey, as well as burrowing into soil to construct nests.
Cranial crests and neural spines
Theropod heads were often decorated with some form of crest, horn, or rugose structure. Although there has been little discussion on the head crests of spinosaurs, Hone and Holtz in 2017 considered that their most likely use was for displaying to potential mates or as a means of threatening rivals and predators. Such has been suggested for theropod cranial structures before, which may have been aided by unusual or bright coloration to provide further visual cues. Many theories have been proposed over the years for the use of spinosaurid dorsal sails, such as thermoregulation; to aid in swimming; to store energy or insulate the animal; or for display purposes, such as intimidating rivals and predators, or attracting mates.
Juvenile spinosaurid fossils are exceedingly rare and almost unknown. However, an ungual phalanx measuring 21 mm (0.83 in) belonging to a very young Spinosaurus indicates that Spinosaurus and probably by extent other spinosaurids, may have developed their semiaquatic adaptations at birth or while at a very young age and maintained these adaptations throughout their lives. The specimen, found in 1999 and described by Simone Maganuco and Cristiano Dal Sasso and colleagues in 2018, is believed to have come from a very small juvenile measuring 1.78 m (5.8 ft), making said specimen the smallest known example of a spinosaurid currently described.
A 2010 publication by Romain Amiot and colleagues found that oxygen isotope ratios of spinosaurid bones indicates semiaquatic lifestyles. Isotope ratios from teeth from Baryonyx, Irritator, Siamosaurus, and Spinosaurus were compared with isotopic compositions from contemporaneous theropods, turtles, and crocodilians. The study found that, among theropods, spinosaurid isotope ratios were closer to those of turtles and crocodilians. Siamosaurus specimens tended to have the largest difference from the ratios of other theropods, and Spinosaurus tended to have the least difference. The authors concluded that spinosaurids, like modern crocodilians and hippopotamuses, spent much of their daily lives in water. The authors also suggested that semiaquatic habits and piscivory in spinosaurids can explain how spinosaurids coexisted with other large theropods: by feeding on different prey items and living in different habitats, the different types of theropods would have been out of direct competition.
In 2018, an analysis was conducted on the partial tibia of an indeterminate spinosaurine from the early Albian, the bone was from a sub-adult between 7–13 m (22–42 ft) in length still growing moderately fast before its death. This specimen (LPP-PV-0042) was found in the Araripe Basin of Brazil and taken to the University of San Carlos for a CT Scan, where it revealed osteosclerosis (high bone density). This condition had previously only been observed in Spinosaurus, as a possible way of controlling its buoyancy. The presence of this condition on the leg fragment showed that semi-aquatic adaptations in spinosaurids were already present at least 10 million years before Spinosaurus aegyptiacus appeared. According to the Phylogenetic bracketing method, this high bone density might have been present in all spinosaurines.
Spinosaurids are known to exist from as early as the Late Jurassic, through characteristic teeth which were found in Tendaguru, Tanzania, and attributed to Ostafrikasaurus. Baryonychines were common, as represented by Baryonyx, which lived during the Barremian of England and Spain. Baryonyx-like teeth are found from the earlier Hauterivian and later Aptian sediments of Spain, as well as the Hauterivian of England, and the Aptian of Niger. The earliest record of spinosaurines is from Africa; they are present in Albian sediments of Tunisia and Algeria, and in Cenomanian sediments of Egypt and Morocco. Spinosaurines are also found in Hauterivian and Aptian-Albian sediments of Thailand, and southern China. In Africa, baronychines were common in the Aptian, and then replaced by spinosaurines in the Albian and Cenomanian.
Some intermediate specimens extend the known range of spinosaurids past the youngest dates of named taxa. A single baryonychine tooth was found from the mid-Santonian, in the Majiacun Formation of Henan, China.
Confirmed spinosaurids have been found on every continent except for North America and Antarctica, the first of which was discovered in 1912 at the Bahariya Formation in Egypt and described in 1915 as Spinosaurus aegyptiacus. Africa has shown a great abundance in spinosaurid discoveries, such as in the Kem Kem beds of Morocco, which housed an ecosystem containing many large coexisting predators. A fragment of a spinosaurine lower jaw from the Early Cretaceous was also reported from Tunisia, and referred to Spinosaurus. Spinosaurinae's range has also extended to South America, particularly Brazil, with the discoveries of Irritator, Angaturama, and Oxalaia. There was also a fossil tooth in Argentina which has been referred to spinosauridae by Leonardo Salgado and colleagues. This referral is doubted by Gengo Tanaka, who offers Hamadasuchus, a crocodilian, as the most likely animal of origin for these teeth.
Baryonychines have been found in Africa, with Suchomimus and Cristatusaurus, as well as in Europe, with Baryonyx and Suchosaurus. Baryonyx-like teeth are also reported from the Ashdown Sands of Sussex, in England, and the Burgos Province, in Spain. A partial skeleton and many fossil teeth indicate spinosaurids were widespread in Asia. As of 2012, three have been named: Ichthyovenator, Siamosaurus and "Sinopliosaurus" fusuiensis. In 2014, a spinosaurid tooth was discovered in Malaysia; the first dinosaur remains discovered in the country. At la Cantalera-1, a site in the Early Barremanian Blesa Formation in Treul, Spain, two types of spinosaurid teeth were found, and they were assigned, tentatively, as indeterminate spinosaurine and baryonychine taxa. An intermediate spinosaurid was discovered in the Early Cretaceous Eumeralla Formation, Australia. It is known from a single 4 cm long partial cervical vertebra, designated NMV P221081. It is missing most of the neural arch. The specimen is from a juvenile estimated to be about 2 to 3 meters long (6–9 ft). Out of all spinosaurs it most closely resembles Baryonyx. In 2019, it was suggested that the vertebra instead belonged to a megaraptorid theropod, as opposed to a spinosaur.
Timeline of genera
Timeline of genera descriptions
- Ibrahim, Nizar; Sereno, Paul C.; Dal Sasso, Cristiano; Maganuco, Simone; Fabri, Matteo; Martill, David M.; Zouhri, Samir; Myhrvold, Nathan; Lurino, Dawid A. (2014). "Semiaquatic adaptations in a giant predatory dinosaur". Science. 345 (6204): 1613–6. Bibcode:2014Sci...345.1613I. doi:10.1126/science.1258750. PMID 25213375. Supplementary Information
- Sereno, Paul C.; Beck, Allison L.; Dutheil, Didier B.; Gado, Boubacar; Larsson, Hans C. E.; Lyon, Gabrielle H.; Marcot, Jonathan D.; Rauhut, Oliver W. M.; Sadleir, Rudyard W. (1998-11-13). "A Long-Snouted Predatory Dinosaur from Africa and the Evolution of Spinosaurids". Science. 282 (5392): 1298–1302. Bibcode:1998Sci...282.1298S. doi:10.1126/science.282.5392.1298. ISSN 0036-8075. PMID 9812890.
- HONE, David William Elliott; HOLTZ, Thomas Richard (2017). "A Century of Spinosaurs - A Review and Revision of the Spinosauridae with Comments on Their Ecology". Acta Geologica Sinica - English Edition. 91 (3): 1120–1132. doi:10.1111/1755-6724.13328. ISSN 1000-9515.
- Dixon, Dougal (2009). The Ultimate Guide to Dinosaurs. Ticktock Books. ISBN 9781846969881.
- Holtz, Thomas R. Jr. (2011) Dinosaurs: The Most Complete, Up-to-Date Encyclopedia for Dinosaur Lovers of All Ages, Winter 2010 Appendix.
- S., Paul, Gregory (2016-10-25). The Princeton field guide to dinosaurs (2nd ed.). Princeton, N.J. ISBN 9781400883141. OCLC 954055249.
- Therrien, François; Henderson, Donald M. (2007-03-12). "My theropod is bigger than yours … or not: estimating body size from skull length in theropods". Journal of Vertebrate Paleontology. 27 (1): 108–115. doi:10.1671/0272-4634(2007)27[108:mtibty]2.0.co;2. ISSN 0272-4634.
- dal Sasso, C.; Maganuco, S.; Buffetaut, E.; Mendez, M.A. (2005). "New information on the skull of the enigmatic theropod Spinosaurus, with remarks on its sizes and affinities". Journal of Vertebrate Paleontology. 25 (4): 888–896. doi:10.1671/0272-4634(2005)025[0888:NIOTSO]2.0.CO;2. ISSN 0272-4634.
- Aureliano, Tito; Ghilardi, Aline M.; Buck, Pedro V.; Fabbri, Matteo; Samathi, Adun; Delcourt, Rafael; Fernandes, Marcelo A.; Sander, Martin (3 May 2018). "Semi-aquatic adaptations in a spinosaur from the Lower Cretaceous of Brazil". Cretaceous Research. 90: 283–295. doi:10.1016/j.cretres.2018.04.024. ISSN 0195-6671.
- Rayfield, Emily J.; Milner, Angela C.; Xuan, Viet Bui; Young, Philippe G. (2007-12-12). "Functional morphology of spinosaur 'crocodile-mimic' dinosaurs". Journal of Vertebrate Paleontology. 27 (4): 892–901. doi:10.1671/0272-4634(2007)27[892:fmoscd]2.0.co;2. ISSN 0272-4634.
- Sues, H. D.; Frey, E.; Martill, D. M.; Scott, D. M. (2002). "Irritator challengeri, a spinosaurid (Dinosauria: Theropoda) from the Lower Cretaceous of Brazil". Journal of Vertebrate Paleontology. 22 (3): 535–547. doi:10.1671/0272-4634(2002)022[0535:ICASDT]2.0.CO;2.
- Sales, M.A.F.; Schultz, C.L. (2017). "Spinosaur taxonomy and evolution of craniodental features: Evidence from Brazil". PLoS ONE. 12 (11): e0187070. Bibcode:2017PLoSO..1287070S. doi:10.1371/journal.pone.0187070. PMC 5673194. PMID 29107966.
- Bertin, Tor (2010-12-08). "A catalogue of material and review of the Spinosauridae". PalArch's Journal of Vertebrate Palaeontology. 7.
- Charig, A. J.; Milner, A. C. (1997). "Baryonyx walkeri, a fish-eating dinosaur from the Wealden of Surrey". Bulletin of the Natural History Museum of London. 53: 11–70.
- Kellner, Alexander W.A.; Sergio A.K. Azevedeo; Elaine B. Machado; Luciana B. Carvalho; Deise D.R. Henriques (2011). "A new dinosaur (Theropoda, Spinosauridae) from the Cretaceous (Cenomanian) Alcântara Formation, Cajual Island, Brazil" (PDF). Anais da Academia Brasileira de Ciências. 83 (1): 99–108. doi:10.1590/S0001-37652011000100006. ISSN 0001-3765.
- Ibrahim, N.; Sereno, P. C.; Dal Sasso, C.; Maganuco, S.; Fabbri, M.; Martill, D. M.; Zouhri, S.; Myhrvold, N.; Iurino, D. A. (2014). "Semiaquatic adaptations in a giant predatory dinosaur". Science. 345 (6204): 1613–1616. Bibcode:2014Sci...345.1613I. doi:10.1126/science.1258750. PMID 25213375.
- Eddy, DR; Clarke, JA (2011). "New Information on the Cranial Anatomy of Acrocanthosaurus atokensis and Its Implications for the Phylogeny of Allosauroidea (Dinosauria: Theropoda)". PLoS ONE. 6 (3): e17932. Bibcode:2011PLoSO...617932E. doi:10.1371/journal.pone.0017932. PMC 3061882. PMID 21445312.
- Hecht, Jeff. 1998. “Fish Swam in Fear.” New Scientist. November 21. https://www.newscientist.com/article/mg16021610-300-fish-swam-in-fear/.
- Allain, R.; Xaisanavong, T.; Richir, P.; Khentavong, B. (2012). "The first definitive Asian spinosaurid (Dinosauria: Theropoda) from the early cretaceous of Laos". Naturwissenschaften. 99 (5): 369–377. Bibcode:2012NW.....99..369A. doi:10.1007/s00114-012-0911-7. PMID 22528021.
- O Estado de S. Paulo (in Portuguese), 2009-05-14, available at ; O Globo, 2009-05-15, abridgement available at ; university's announcement at Moutinho, Sofia (2009-11-05). "Inaugura dia 14 a exposição Dinossauros no Sertão". Archived from the original on 2011-07-06. Retrieved 2010-01-13.
- Machado, E. B.; Kellner, A. W. A.; Campos, D. A. (2005). "Preliminary information on a dinosaur (Theropoda, Spinosauridae) pelvis from the Cretaceous Santana Formation (Romualdo Member) Brazil". Congresso Latino-Americano de Paleontologia de Vertebrados. 2 (Boletim de resumos): 161–162.
- Evers, Serjoscha W.; Rauhut, Oliver W.M.; Milner, Angela C.; McFeeters, Bradley; Allain, Ronan (2015-10-20). "A reappraisal of the morphology and systematic position of the theropod dinosaurSigilmassasaurusfrom the "middle" Cretaceous of Morocco". PeerJ. 3: e1323. doi:10.7717/peerj.1323. ISSN 2167-8359. PMC 4614847. PMID 26500829.
- Mantell, G.A., 1822, The fossils of the South Downs or Illustrations of the Geology of Sussex, London, Rupton Relfe
- Owen, R. (1840–1845). Odontography. London: Hippolyte Baillière, 655 pp, 1–32
- Owen, R., 1842, Report on British fossil reptiles. Part II. Reports of the meetings of the British Association for the Advancement of Science. 11, pp 61-204
- Sauvage, H. E. (1897–1898). Vertébrés fossiles du Portugal. Contribution à l’étude des poissons et des reptiles du Jurassique et du Crétacique. Lisbonne: Direction des Travaux géologiques du Portugal, 46p
- Milner, A., 2003, "Fish-eating theropods: A short review of the systematics, biology and palaeobiogeography of spinosaurs". In: Huerta Hurtado and Torcida Fernandez-Baldor (eds.). Actas de las II Jornadas Internacionales sobre Paleontologýa de Dinosaurios y su Entorno (2001). pp 129-138
- Smith, Joshua B.; Lamanna, Matthew C.; Mayr, Helmut; Lacovara, Kenneth J. (2006-03-01). "New information regarding the holotype of spinosaurus aegyptiacus". Journal of Paleontology. 80 (2): 400–406. doi:10.1666/0022-3360(2006)080[0400:NIRTHO]2.0.CO;2. ISSN 0022-3360.
- HONE, David William Elliott; HOLTZ, Thomas Richard (June 2017). "A Century of Spinosaurs - A Review and Revision of the Spinosauridae with Comments on Their Ecology". Acta Geologica Sinica - English Edition. 91 (3): 1120–1132. doi:10.1111/1755-6724.13328. ISSN 1000-9515.
- Stromer, E. (1934). "Ergebnisse der Forschungsreisen Prof. E. Stromers in den Wüsten Ägyptens. II. Wirbeltier-Reste der Baharije-Stufe (unterstes Cenoman). 13. Dinosauria". Abhandlungen der Bayerischen Akademie der Wissenschaften Mathematisch-naturwissenschaftliche Abteilung, Neue Folge (in German). 22: 1–79.
- Sereno, Paul C., Allison L. Beck, Didier B. Dutheil, Boubacar Gado, Hans C. E. Larsson, Gabrielle H. Lyon, Jonathan D. Marcot, et al. 1998. “A Long-Snouted Predatory Dinosaur from Africa and the Evolution of Spinosaurids.” Science 282 (5392): 1298–1302. doi:10.1126/science.282.5392.1298.
- Rayfield, Emily J. 2011. “Structural Performance of Tetanuran Theropod Skulls, with Emphasis on the Megalosauridae, Spinosauridae and Carcharodontosauridae.” Special Papers in Palaeontology 86 (November). https://www.researchgate.net/publication/250916680_Structural_performance_of_tetanuran_theropod_skulls_with_emphasis_on_the_Megalosauridae_Spinosauridae_and_Carcharodontosauridae.
- Buffetaut, Eric, and Mohamed Ouaja. 2002. “A New Specimen of Spinosaurus (Dinosauria, Theropoda) from the Lower Cretaceous of Tunisia, with Remarks on the Evolutionary History of the Spinosauridae.” Bulletin de La Société Géologique de France 173 (5): 415–21. doi:10.2113/173.5.415.
- Arden, T.M.S.; Klein, C.G.; Zouhri, S.; Longrich, N.R. (2018). "Aquatic adaptation in the skull of carnivorous dinosaurs (Theropoda: Spinosauridae) and the evolution of aquatic habits in Spinosaurus". Cretaceous Research. In Press: 275–284. doi:10.1016/j.cretres.2018.06.013.
- Sues, Hans-Dieter, Eberhard Frey, David M. Martill, and Diane M. Scott. 2002. “Irritator Challengeri, a Spinosaurid (Dinosauria: Theropoda) from the Lower Cretaceous of Brazil.” Journal of Vertebrate Paleontology 22 (3): 535–47. doi:10.1671/0272-4634(2002)022[0535:ICASDT]2.0.CO;2.
- Vullo, R.; Allain, R.; Cavin, L. (2016). "Convergent evolution of jaws between spinosaurid dinosaurs and pike conger eels". Acta Palaeontologica Polonica. 61. doi:10.4202/app.00284.2016.
- Rayfield, Emily J., Angela C. Milner, Viet Bui Xuan, and Philippe G. Young. 2007. “Functional Morphology of Spinosaur ‘crocodile-Mimic’ Dinosaurs.” Journal of Vertebrate Paleontology 27 (4): 892–901. doi:10.1671/0272-4634(2007)27[892:FMOSCD]2.0.CO;2.
- Cuff, Andrew R., and Emily J. Rayfield. 2013. “Feeding Mechanics in Spinosaurid Theropods and Extant Crocodilians.” PLOS ONE 8 (5): e65295. doi:10.1371/journal.pone.0065295.
- Witton, Mark P. (2018-01-01). "Pterosaurs in Mesozoic food webs: a review of fossil evidence". Geological Society, London, Special Publications. 455 (1): 7–23. Bibcode:2018GSLSP.455....7W. doi:10.1144/SP455.3. ISSN 0305-8719.
- Buffetaut, Eric, David Martill, and François Escuillié. 2004. “Pterosaurs as Part of a Spinosaur Diet.” Nature 430. doi:10.1038/430033a.
- Sales, Marcos A. F.; Lacerda, Marcel B.; Horn, Bruno L. D.; Oliveira, Isabel A. P. de; Schultz, Cesar L. (2016-02-01). "The "χ" of the Matter: Testing the Relationship between Paleoenvironments and Three Theropod Clades". PLOS ONE. 11 (2): e0147031. Bibcode:2016PLoSO..1147031S. doi:10.1371/journal.pone.0147031. ISSN 1932-6203. PMC 4734717. PMID 26829315.
- Hassler, A.; Martin, J. E.; Amiot, R.; Tacail, T.; Godet, F. Arnaud; Allain, R.; Balter, V. (2018). "Calcium isotopes offer clues on resource partitioning among Cretaceous predatory dinosaurs". Proceedings of the Royal Society B: Biological Sciences. 285 (1876): 20180197. doi:10.1098/rspb.2018.0197. PMC 5904318. PMID 29643213.
- Charig, A. J.; Milner, A. C. (1986). "Baryonyx, a remarkable new theropod dinosaur". Nature. 324 (6095): 359–361. Bibcode:1986Natur.324..359C. doi:10.1038/324359a0. PMID 3785404.
- Kitchener, Andrew (1987). "Function of Claws' claws". Nature. 325 (6100): 114. Bibcode:1987Natur.325..114K. doi:10.1038/325114a0. ISSN 0028-0836.
- Therrien, F.; Henderson, D.; Ruff, C. (2005). "Bite me – biomechanical models of theropod mandibles and implications for feeding behavior". In Carpenter, K. (ed.). The Carnivorous Dinosaurs. Indiana University Press. pp. 179–230. ISBN 978-0-253-34539-4.
- Carpenter, Kenneth (2005). The Carnivorous Dinosaurs. Indiana University Press. pp. 285–291. ISBN 9780253345394.
- Halstead, L.B. (1975). The Evolution and Ecology of the Dinosaurs. London: Eurobook Limited. pp. 1–116. ISBN 978-0-85654-018-9.
- "Gimsa, J., Sleigh, R., Gimsa, U., (2015) : "The riddle of Spinosaurus aegyptiacus ' dorsal sail". University of Rostock, Chair for Biophysics, Gertrudenstr. 11A, 18057 Rostock, Germany". Cite journal requires
- Bailey, J.B. (1997). "Neural spine elongation in dinosaurs: sailbacks or buffalo-backs?". Journal of Paleontology. 71 (6): 1124–1146. doi:10.1017/S0022336000036076. JSTOR 1306608.
- Stromer, E. (1915). "Ergebnisse der Forschungsreisen Prof. E. Stromers in den Wüsten Ägyptens. II. Wirbeltier-Reste der Baharije-Stufe (unterstes Cenoman). 3. Das Original des Theropoden Spinosaurus aegyptiacus nov. gen., nov. spec". Abhandlungen der Königlich Bayerischen Akademie der Wissenschaften, Mathematisch-physikalische Klasse (in German). 28 (3): 1–32.[permanent dead link]
- "The smallest biggest theropod dinosaur: A new fossil from Africa represents a small juvenile individual of the huge sail-backed Spinosaurus".
- Amiot, R.; Buffetaut, E.; Lécuyer, C.; Wang, X.; Boudad, L.; Ding, Z.; Fourel, F.; Hutt, S.; Martineau, F.; Medeiros, A.; Mo, J.; Simon, L.; Suteethorn, V.; Sweetman, S.; Tong, H.; Zhang, F.; Zhou, Z. (2010). "Oxygen isotope evidence for semi-aquatic habits among spinosaurid theropods". Geology. 38 (2): 139–142. Bibcode:2010Geo....38..139A. doi:10.1130/G30402.1.
- Buffetaut, Eric. 2008. “Spinosaurid Teeth from the Late Jurassic of Tendaguru, Tanzania, with Remarks on the Evolutionary and Biogeographical History of the Spinosauridae.” https://www.academia.edu/3101178/Spinosaurid_teeth_from_the_Late_Jurassic_of_Tendaguru_Tanzania_with_remarks_on_the_evolutionary_and_biogeographical_history_of_the_Spinosauridae
- Hone, Dave, Xing Xu, Deyou Wang, and Vertebrata PalAsiatica. 2010. “A Probable Baryonychine (Theropoda: Spinosauridae) Tooth from the Upper Cretaceous of Henan Province, China (PDF Download Available).” ResearchGate. January. https://www.researchgate.net/publication/271967379_A_probable_Baryonychine_Theropoda_Spinosauridae_tooth_from_the_Upper_Cretaceous_of_Henan_Province_China.
- Benyoucef, Madani, Emilie Läng, Lionel Cavin, Kaddour Mebarki, Mohammed Adaci, and Mustapha Bensalah. 2015. “Overabundance of Piscivorous Dinosaurs (Theropoda: Spinosauridae) in the Mid-Cretaceous of North Africa: The Algerian Dilemma.” Cretaceous Research 55 (July): 44–55. doi:10.1016/j.cretres.2015.02.002.
- Hendrickx, Christophe, Octávio Mateus, and Eric Buffetaut. 2016. “Morphofunctional Analysis of the Quadrate of Spinosauridae (Dinosauria: Theropoda) and the Presence of Spinosaurus and a Second Spinosaurine Taxon in the Cenomanian of North Africa.” PLOS ONE 11 (1): e0144695. doi:10.1371/journal.pone.0144695.
- Salgado, Leonardo, José I. Canudo, Alberto C. Garrido, José I. Ruiz-Omeñaca, Rodolfo A. García, Marcelo S. de la Fuente, José L. Barco, and Raúl Bollati. 2009. “Upper Cretaceous Vertebrates from El Anfiteatro Area, Río Negro, Patagonia, Argentina.” Cretaceous Research 30 (3): 767–84. doi:10.1016/j.cretres.2009.01.001.
- Tanaka, Gengo. 2017. “Fine Sculptures on a Tooth of Spinosaurus (Dinosauria, Theropoda) from Morocco.” Bulletin of Gunma …. Accessed May 30. https://www.academia.edu/1300482/Fine_sculptures_on_a_tooth_of_Spinosaurus_Dinosauria_Theropoda_from_Morocco.
- Sereno, P.C.; Beck, A.L.; Dutheil, D.B.; Gado, B.; Larsson, H.C.E.; Lyon, G.H.; Marcot, J.D.; Rauhut, O.W.M.; Sadleir, R.W.; Sidor, C.A.; Varricchio, D.D.; Wilson, G.P; Wilson, J.A. (1998). "A long-snouted predatory dinosaur from Africa and the evolution of spinosaurids". Science. 282 (5392): 1298–1302. Bibcode:1998Sci...282.1298S. doi:10.1126/science.282.5392.1298. PMID 9812890. Retrieved 2013-03-19.
- Taquet, P. and Russell, D.A. (1998). "New data on spinosaurid dinosaurs from the Early Cretaceous of the Sahara". Comptes Rendus de l'Académie des Sciences à Paris, Sciences de la Terre et des Planètes 327: 347-353
- Mateus, O.; Araújo, R.; Natário, C.; Castanhinha, R. (2011). "A new specimen of the theropod dinosaur Baryonyx from the early Cretaceous of Portugal and taxonomic validity of Suchosaurus" (PDF). Zootaxa. 2827. 2827: 54–68. doi:10.11646/zootaxa.2827.1.3.
- ResearchSEA (2014). "First discovery of dinosaur fossils in Malaysia". ScienceDaily.
- Alonso, Antonio, and José Ignacio Canudo. 2016. “On the Spinosaurid Theropod Teeth from the Early Barremian (Early Cretaceous) Blesa Formation (Spain).” Historical Biology 28 (6): 823–34. doi:10.1080/08912963.2015.1036751.
- "Australian 'Spinosaur' unearthed". Australian Geographic. Retrieved 2018-04-15.
- Barrett, P. M.; Benson, R. B. J.; Rich, T. H.; Vickers-Rich, P. (2011). "First spinosaurid dinosaur from Australia and the cosmopolitanism of Cretaceous dinosaur faunas". Biology Letters. 7 (6): 933–936. doi:10.1098/rsbl.2011.0466. ISSN 1744-9561. PMC 3210678. PMID 21693488.
- Poropat, Stephen F.; White, Matt A.; Vickers-Rich, Patricia; Rich, Thomas H. (2019). "New megaraptorid (Dinosauria: Theropoda) remains from the Lower Cretaceous Eumeralla Formation of Cape Otway, Victoria, Australia". Journal of Vertebrate Paleontology: e1666273. doi:10.1080/02724634.2019.1666273.
- Spinosauridae on the Theropod Database