From Wikipedia, the free encyclopedia
Jump to navigation Jump to search

Temporal range: Late Cretaceous,
~70 Ma
Therizinosaurus arms.jpg
Mounted forelimbs of specimen MPC-D 100/15 at Nagoya City Science Museum
Scientific classification e
Kingdom: Animalia
Phylum: Chordata
Clade: Dinosauria
Clade: Saurischia
Clade: Theropoda
Superfamily: Therizinosauroidea
Family: Therizinosauridae
Genus: Therizinosaurus
Maleev, 1954
Type species
Therizinosaurus cheloniformis
Maleev, 1954

Therizinosaurus (/ˌθɛrɪˌzɪnˈsɔːrəs/; meaning 'scythe lizard') is a genus of very large therizinosaurid that lived in Asia during the Late Cretaceous period in what is now the Nemegt Formation around 70 million years ago. It contains the single type species Therizinosaurus cheloniformis. The first remains of Therizinosaurus were found in 1948 by a Mongolian field expedition at the Gobi Desert and later described by Evgeny Maleev in 1954. The genus is known only from a few bones, including gigantic manual unguals (claw bones), from which it gets its name, and additional findings comprising fore and hindlimb elements that have been discovered during the 1960s–1980s.

Therizinosaurus was a colossal therizinosaur that could grow up to 9–10 m (30–33 ft) long and weigh possibly over 3 t (3,000 kg). Like other therizinosaurs, it would have been a slow-moving, long-necked high browser equipped with a rhamphotheca (horny beak) and a wide torso for food processing. The forelimbs were particularly robust and had three fingers that bore unguals which, unlike other relatives, were very stiffened, elongated, and only had significant curvatures at the tips. Therizinosaurus had the longest known manual unguals of any land animal, reaching above 50 cm (500 mm) in length. Its hindlimbs ended in four functionally weight-bearing toes differing from other theropod groups in which the first toe was reduced to a dewclaw and also resembling the unrelated sauropodomorphs.

It was one of the last and the largest representative of its unique group, the Therizinosauria (formerly known as Segnosauria; the segnosaurs). During and after its original description in 1954, Therizinosaurus had rather complex relationships due to the lack of complete specimens and relatives at the time. Maleev thought the remains of Therizinosaurus to belong to a large turtle-like reptile, and also named a separate family for the genus: Therizinosauridae. Later on, with the discovery of more complete relatives, Therizinosaurus and kin were thought to represent some kind of Late Cretaceous sauropodomorphs or transitional ornithischians, even though at some point it was suggested that it may have been a theropod. After years of taxonomic debate, nevertheless, they are now placed in one of the major dinosaur clades, Theropoda, specifically as maniraptorans. Therizinosaurus is widely recovered within Therizinosauridae by most analyses.

The unusual arms and body anatomy (extrapolated after relatives) of Therizinosaurus have been cited as an example of convergent evolution with chalicotheriines and other primarily herbivorous mammals, suggesting similar feeding habits. The elongated hand claws of Therizinosaurus were more useful when pulling vegetation within reach rather than being used for active attack or defense because of their fragility, however, they may have had some role for intimidation. Its arms also were particularly resistant to stress, which suggests a robust use of these limbs. Therizinosaurus was a very tall animal, likely having a reduced competition over the foliage in its habitat and outmatching predators like Tarbosaurus.

History of discovery[edit]

Cretaceous fossil localities of Mongolia; Therizinosaurus fossils have been collected from the Altan Uul, Hermiin Tsav, and Nemegt localities at the area A (Nemegt Formation)

In 1948, several Mongolian Paleontological expeditions organized by the USSR Academy of Sciences were conducted in the Nemegt Formation of the Gobi Desert, Southwestern Mongolia, with the main objective of new fossils findings. The expeditions unearthed numerous dinosaur and turtle fossil remains from the stratotype locality Nemegt (also known as Nemegt Valley), but the most notable elements collected were three partial manual unguals (claw bones) of considerable size. This set of unguals was found on a subdivision of the Nemegt locality designated as Quarry V near the skeleton of a large theropod, but also in association with other elements including a metacarpal fragment and several ribs fragments. It was labelled under the specimen number PIN 551-483 and later on, these fossils were described by the Russian paleontologist Evgeny Maleev in 1954 who used them to scientifically name the new genus and type species Therizinosaurus cheloniformis, becoming the holotype specimen. The generic name, Therizinosaurus, is derived from the Greek θερίζω (therízo, meaning scythe, reap or cut) and σαῦρος (sauros, meaning lizard) in reference to the enormous manual unguals, and the specific name, cheloniformis, is taken from the Greek χελώνη (chelóni, meaning turtle) and Latin formis as the remains were thought to belong to a turtle-like reptile. Maleev also coined a separate family for this new and enigmatic taxon: Therizinosauridae. Since little was known of Therizinosaurus at the time of the original description, Maleev thought PIN 551-483 belonged to a large, 4.5 m (15 ft) long marine turtle that relied on its giant hand claws to harvest seaweed.[1]

Holotype unguals PIN 551–483 at the Moscow Paleontological Museum; note left ungual cast

Though it was not fully understood what general kind of animal these fossils belonged, in 1970 the Russian paleontologist Anatoly K. Rozhdestvensky was one of the first authors to suggest that Therizinosaurus was a theropod and not a turtle. He made comparisons between Chilantaisaurus and the holotype unguals of Therizinosaurus to propose that these appendages actually came from a carnosaurian dinosaur, thereby interpreting Therizinosaurus as a theropod. Rozhdestvensky also illustrated the three holotypic manual unguals and re-identified the metacarpal fragment as a metatarsal bone, and based on the unusual shape of both metatarsal and ribs fragments he listed them as sauropod remains.[2] These theropodan affinities were also followed by the Polish paleontologist Halszka Osmólska and co-author Ewa Roniewicz in 1970 during their naming and description of Deinocheirus—another large and enigmatic theropod from the formation that was initially known from partial arms. Similar to Rozhdestvensky, they suggested that the holotype unguals were more likely to have belonged to a carnosaurian theropod, rather than a large marine turtle.[3]

Additional specimens[edit]

Arms of specimen MPC-D 100/15 with unguals 100/16 and 100/17 at CosmoCaixa Barcelona

Further expeditions in the Nemegt Formation unearthed more fossils of Therizinosaurus. In 1968 prior to Rozhdestvensky, Osmólska and Roniewicz statements, the upper portion of a manual ungual was found in the Altan Uul locality and labeled as MPC-D 100/17 (formerly IGM or GIN). In 1972, another fragmented ungual (specimen MPC-D 100/16) was discovered at the Upper White Beds of the Hermiin Tsav locality, only preserving its lower portion.[4][5] During the year 1973, a much more complete, larger, and articulated specimen was collected also from Hermiin Tsav. This specimen was labelled as MPC-D 100/15 and consists of both left and right arms including the scapulocoracoids, both humeri (upper arm bones), right ulna with radius and left ulna, two right carpals, the right metacarpus including a complete digit Il, and some ribs with gastralia (belly ribs). As common with fossils, some elements were not entirely preserved such as the scapulocoracoids with broken ends, and the left arm is less complete than the right one. All of these specimens were first described and referred to Therizinosaurus by the Mongolian paleontologist Rinchen Barsbold in 1976. In this new monograph, he pointed out that the rib fragments in MPC-D 100/15 were more slender than the ones from the holotype, and identified MPC-D 100/16 and 100/17 as pertaining to digits I and III, respectively. It was clear to Barsbold that MPC-D 100/15 represented Therizinosaurus as the ungual in this specimen shared the elongation and flattened morphology of all previous specimens. He concluded that Therizinosaurus was a theropod taxon since MPC-D 100/15 matched multiple theropodan characters.[4]

Composite skeletal of the known remains of Therizinosaurus

Also during the year 1973, the specimen MPC-D 100/45 was discovered by the Joint Soviet-Mongolian Paleontological Expedition at the Hermiin Tsav locality. Unlike the previous findings, MPC-D 100/45 is represented by a right hindlimb composed of a very fragmented femur with the lower end of the tibia, astragalus, calcaneum, tarsal IV, a functional tetradacyl feet (four-toed) compromising four partial metatarsals, partially preserved digits I and III, and nearly complete digits II and IV. These newer remains were described by the also Mongolian paleontologist Altangerel Perle in 1982. He regarded the referral of Therizinosaurus and Therizinosauridae to Chelonia (turtles order) to be unlikely, and hypothesized Therizinosaurus and Segnosaurus—at the time of this description regarded as a theropod dinosaur—to be particularly similar based on their respective scapulocoracoid morphology, only differing in size. Perle referred MPC-D 100/45 to Therizinosaurus given that this specimen was found near the location of MPC-D 100/15 and was virtually similar to the described pes for Segnosaurus.[6] In 1990, Barsbold and Teresa Maryanska agreed with Perle in that the hindlimb material from Hermiin Tsav he described in 1982 was therizinosaurian (then called segnosaurians) given that the metatarsus was stocky and the astragalus had a laterally arched ascending process (bony extension), but cast doubt with his referral of it to Therizinosaurus and the segnosaurian identity for this taxon since it was only known from the pectoral girdle and other forelimb elements, making direct comparisons between specimens impossible. They considered this specimen to represent a Late Cretaceous representative of the Segnosauria, but not Therizinosaurus.[7]

In 2010 however, the North American paleontologist Lindsay E. Zanno in her large taxonomic reevaluation of Therizinosauria considered the referral of MPC-D 100/45 to Therizinosaurus to be likely based on the rationale that it was collected in the same stratigraphic context (Nemegt Formation) as the holotype, and shared the robust and four-toed morphology of other therizinosaurids such as Segnosaurus. She also excluded the rib material from the holotype as it was re-identified by Rozhdestvensky to likely have come from a sauropod dinosaur, and not Therizinosaurus itself.[8]


Size of two specimens (holotype in yellow, right) compared to a 1.8 m (5.9 ft) tall human

For maniraptoran standards, Therizinosaurus obtained enormous sizes, estimated to have reach 9 to 10 m (30 to 33 ft) in length with ponderous weights from 3 t (3,000 kg) to possibly over 5 t (5,000 kg).[9][10][11] These dimensions make Therizinosaurus the largest therizinosaur known and the largest known maniraptoran. Along with the contemporaneous ornithomimosaur Deinocheirus, it was the largest maniraptoriform.[12] Though the body remains of Therizinosaurus are relatively incomplete, inferences can be made about its physical characteristics based on more complete and related therizinosaurids. Like other members of its family, Therizinosaurus had a proportionally small skull bearing a rhamphotheca (horny beak) atop its long neck; bipedal gaits; a large belly for foliage processing; and sparse feathering. Other traits that were likely present in Therizinosaurus include a heavily pneumatized (air-filled) vertebral column and a robustly-built, ophistopubic (backwards oriented) pelvis.[13][14][15]

In 2010, Senter and James used hindlimb length equations to predict the total length of the hindlimbs in Therizinosaurus and Deinocheirus. They concluded that an average Therizinosaurus may have had approximately 3 m (9.8 ft) long legs.[16] More recently, Mike Taylor and Matt Wedel suggested that the whole neck would be 2.9 times the size of the humerus, which was 76 cm (760 mm), resulting in a 2.2 m (7.2 ft) long neck based on comparisons with the cervical vertebrae series of Nanshiungosaurus.[17] The most distinctive feature of Therizinosaurus was the presence of gigantic unguals on each of the three digits of its hands. These were common among therizinosaurs but particularly large and stiffened in Therizinosaurus, and they are considered as the longest known from any terrestrial animal.[12]


Diagram of the right arm and shoulder blade (rotated) of MPC-D 100/15

The arm of Therizinosaurus covered 2.4 m (7.9 ft) in total length (humerus, radius and second metacarpal with phalanges lengths).[16] The scapula measured 67 cm (670 mm) long with a stocky and flattened dorsal blade, wide acromial process (bony extension) and a very widened ventral surface. Near the anterior edge of the scapular widening and near the scapulocoracoid suture (bone joint), a foramen was located; it likely functioned as a channel for blood vessels and nerves when alive. The posterior edge of the scapula was robust and the acromion was lightly built, likely fused into a cartilaginous system with its periphery in life. The coracoid measured 36 cm (360 mm) in length, it had a broad and convex lateral surface that formed a slightly inclined concavity near of the scapulocoracoid suture. This concavity bent down towards the scapular widening. Near the scapulocoracoid suture, this edge turned very thin and possibly into cartilage along with the periphery of the coracoid in life, as the case of the scapular edge. A large foramen was also present on the coracoid. The glenoid was broad and deep, slightly pointing to the outer lateral side. It had robust and convex crest-like borders. The supraglenoid thickness was developed in a convex crest-shaped form, it was divided across the top of the scapulocoracoid suture. The attachment for the biceps muscle was prominently developed by a large tubercle with a stocky top, indicating powerful muscles in life.[4][18][8]

The humerus was robustly built, measuring 76 cm (760 mm) long. It had a broad upper end. The deltopectoral crest (deltoid muscle attachment) was particularly long and thick, with its top located approximately 1/3 from the upper end. The length of the crest was no less than 2/3 the length of the whole bone element. The lower end of the humerus was very expanded and flared. The condyles were developed onto the anterior side of the lower expansion while the epicondyles were very broad and projected over the limits of the articular areas. The ulna measured 62.02 cm (620.2 mm) and most of its length was occupied by its straight shaft. The ulnar process was very wide. The upper articular area was divided into inner and outer lateral sides. The lateral side had a triangular-shaped border and was slightly concave; it was limited in a top view by the depression for the upper articulation of the radius. The inner side formed a semilunar-shaped depression that covered the lunar-shaped condyle of the humerus. The radius was 55.04 cm (550.4 mm) long and slightly S-curved. Its upper end was flattened in a lateral direction, very wide, and the distal end was highly robust.[4][18][8]

Skeletal diagram featuring the known unguals of Therizinosaurus

The first lower carpal bone measured 8.23 cm (82.3 mm) tall and 8.53 cm (85.3 mm) wide and had two articulation surfaces on its lowermost end. The upper surface of this carpal was divided by a broad depression that formed the articulation of the carpus. On its inner side, it had a triangular-shaped outline that attached to the upper surface of metacarpal I, occupying a little bit less than the lateral side, which articulates to metacarpal II. These areas were separated by an oblique bony projection. The second lower carpal was smaller than the first one, measuring 5.6 cm (56 mm) tall and 5.93 cm (59.3 mm) wide. Its lower surface was flattened and the articular surface of the carpus extended from the first carpal to the second carpal over the articulation of the two bones.[4][18][8]

The metacarpal I was 14.55 cm (145.5 mm) long and compared to the others it was more stockier. Its lateral side was broad, especially on the uppermost area; the inner border was thin and narrow. The upper articulation was configured into three parts. The lower articular surface was somewhat asymmetric and bent to the inner side from the left one, along with a wide and deep opening. The total length of this metacarpal was larger than 2/3 the length of metacarpal III, which may have been a unique trait of Therizinosaurus. The metacarpal II measured 28.68 cm (286.8 mm) in length and was the most elongated and robust metacarpal. It had an inclined, square-shaped, and flattened upper articulation. The articulation on the lower head had very symmetrical condyles, being divided by a broad, deep depression. The lateral connecting openings were poorly developed. The metacarpal III covered 19.16 cm (191.6 mm) in length and had a very thin shaft compared to the other metacarpals. Its upper articulation was divided into three parts. The lower articular head was asymmetrical with deep and broad openings. As in metacarpal II, the lateral connecting openings were poorly developed.[4][18][8]

Only the second digit of the manus is known in Therizinosaurus. It consisted of two phalanges and a large ungual. The first and second phalanges were somewhat equal in shape and length (14.17 cm (141.7 mm) and 14.38 cm (143.8 mm), respectively), and shared the robust and stocky structure. The upper articular facets were very symmetrical and had a crest—particularly taller in the first phalanx. The top border of this crest was very pointed and thick; it likely served as the site for attachment of the extensor tendons in life. The lower heads were nearly symmetrical, but the central depression was considerably wider and deeper in the first phalanx. The manual unguals of Therizinosaurus were especially enormous and long, estimated to have covered approximately 52 cm (520 mm) in length. Unlike other therizinosaurs they were very straight, side to side flattened, and had sharp curvatures only at the tips, a unique feature of Therizinosaurus. The lower tubercle, where the flexor tendons attached to the ungual, was thick and robust, indicating a large pad in life. The articulation surface that connected the preceding phalanx was slightly concave and divided into two by a central ridge.[4][18][8]


Labelled diagram of the referred pes specimen MPC-D 100/45

Therizinosaurus had a rather stocky and robust tibia that was very wide on its lower end. The metatarsus was robust and short (almost sauropodomorph-like), and composed of five metatarsals. The first four were functional and terminated in weight-bearing digits, hence having a tetradactyl (four-toed) condition. The last or fifth metatarsal was highly reduced bone located at the lateral side of the metatarsus and had no functional significance. Unlike most other theropods groups, the first pedal digit was—though shorter than the others—functional and weight-bearing. The second and third were equally long while the fourth was smaller and somewhat thinner. The pedal unguals were side to side flattened and likely sharp. The morphology of the feet of Therizinosaurus and other therizinosaurids was unique, as the general theropod formula includes tridactyl (three-toed) feet in which the first toe was reduced to a dewclaw and held off the ground.[6][15]


Outdated quadrupedal, sauropodomorph-like restoration of Erlikosaurus

Maleev originally classified Therizinosaurus as to have been a giant marine turtle and the genus was assigned by Maleev to a separate Therizinosauridae given how enigmatic the specimen was.[1] The fossils remained with uncertainty among the scientific community, however, in 1970 Rozhdestvensky was one of the first paleontologists suggesting that Therizinosaurus was actually a theropod dinosaur instead of some turtle. He also suggested that the supposed ribs of the holotype were likely from a different dinosaur, possibly some sauropodomorph.[2] In 1976 Barsbold concluded that Therizinosaurus was a theropod because MPC-D 100/15 matched numerous theropodan characters and Therizinosauridae with Deinocheiridae were probably synonyms.[4] With the discovery and description of Segnosaurus, in 1979 Perle named a new family of dinosaurs, the Segnosauridae. He tentatively placed the family within Theropoda given the similarities of the mandible and dentition to other members.[19] A year later, the new genus Erlikosaurus was named by Barsbold and Perle in 1980. They named a new infraorder called the Segnosauria, composed by Erlikosaurus and Segnosaurus. They also noted that while aberrant and having ornithischian-like pelves, segnosaurs featured similar traits to other theropods.[20] With the discovery of the referred hindlimb to Therizinosaurus in 1982 by Perle, he concluded that Segnosaurus was very similar to the latter based on the pes morphology and they possibly belonged to a single, if not the same group.[6] In 1983, Barsbold named a new genus of segnosaur Enigmosaurus. He analyzed the pelvis of this new genus and pointed out that segnosaurids were so different from other theropods that they could be outside the group or represent a different lineage of theropod dinosaurs.[18] Later on the same year, he intensified the exclusion of segnosaurs from being theropods by noting that their pelves resembled those of sauropod dinosaurs.[21]

Mounted skeleton of Alxasaurus at the Royal Tyrrell Museum. Alxasaurus helped to resolve important aspects about the affinities of the long-enigmatic therizinosaurs

Consequently, the assignment of segnosaurs started to shift towards sauropodomorphs. In 1984, Gregory S. Paul claimed that segnosaurs rather than being aberrant theropods were indeed, sauropodomorphs which successfully managed to remain into the Cretaceous period. He based this idea on anatomical traits such as the skull and similar pes configuration.[22] He maintained his position in 1988 by placing the Segnosauria into the now obsolete Phytodinosauria, and was one of the first to suggest a segnosaur assignment for the enigmatic Therizinosaurus.[23] Other prominent paleontologists like Jacques Gauthier or Paul Sereno supported this vision.[24][25] In 1990, Barsbold and Teresa Maryanska agreed in that the hindlimb material from Hermiin Tsav referred to Therizinosaurus in 1982 was segnosaurian since it matched several traits, but considered it unlikely to belong to the genus and species as there was no overlapping material among specimens. Barsbold and Maryanska also disagreed with previous researchers who classified Deinocheirus as a segnosaur.[7] In the same year, David B. Norman considered Therizinosaurus to be a theropod of uncertain classification.[26]

Feather impressions from the holotype of Beipiaosaurus

However, with the unexpected discovery and description of Alxasaurus in 1993, the widely accepted sauropodomorph affinities of segnosaurs were questioned by paleontologists Dale Russell and Dong Zhiming. This new genus was far more complete than any other segnosaur and multiple anatomical features indicated that it was related to Therizinosaurus. With this, they identified the Therizinosauridae along with the Segnosauridae to be the same group, the former name having taxonomic priority. Due to some primitive characters present in Alxasaurus they coined a new taxonomic rank, the Therizinosauroidea, containing this new taxon and the Therizinosauridae. All of this new information provided data on the affinities of the new-named therizinosauroids. Lastly, Russell and Dong concluded that these animals were actual theropods with unusually aberrant features.[27] In 1994, Clark and colleagues redescribed the very complete skull of Erlikosaurus and even more theropod traits were found this time. They also validated the synonymy of the Segnosauridae with Therizinosauridae and considered therizinosauroids as maniraptoran dinosaurs.[28] In 1997, Rusell coined the infraorder Therizinosauria in order to contain all segnosaurs. This new infraorder was composed of Therizinosauroidea and the more advanced Therizinosauridae. Consequently, Segnosauria became a synonym of Therizinosauria.[29] Though some uncertainties remained, a small and feathered therizinosauroid from China was described in 1999 by Xu Xing and colleagues, the new genus Beipiaosaurus. It definitely confirmed the placement of therizinosaurs among theropods and also their taxonomic place on the Coelurosauria. This discovery also indicated that feathers were highly distributed among theropod dinosaurs.[30]

In 2010, Lindsay Zanno revised the taxonomy of therizinosaurs with extensive detail. She found that many parts on therizinosaur holotype and referred specimens were lost or damaged, and sparse specimens with no overlapping elements were disadvantages when concluding the relationships of the members. Zanno accepted the referral of the specimen IGM 100/45 to Therizinosaurus since it matches multiple therizinosaurid traits but decided not to include the specimen in her taxonomic analysis due to the lack of comparative forelimb remains. She also excluded the supposed ribs that were present on the holotype since they likely came from a different animal and not Therizinosaurus.[8] In 2019, Hartman and colleagues also performed a large phylogenetic analysis of Therizinosauria based on the characters provided by Zanno in her revision. They found similar results to Zanno regarding the family Therizinosauridae but this time with the inclusion of more taxa and specimens. Cladogram below shows the placement of Therizinosaurus within Therizinosauria according to Hartman and colleagues in 2019:[31]

Skeletal reconstructions of various therizinosaurian genera (not to scale); Therizinosaurus in top left

Suzhousaurus Suzhousaurus.JPG


Neimongosaurus Neimongosaurus.jpg


Therizinosaurus Therizinosaurus Restoration.png

Erliansaurus Erliansaurus bellamanus.jpg


Nanchao embryos THERIZINOSAURUS.jpg


Nanshiungosaurus Nanshiungosaurus Restoration.png


Segnosaurus Segnosaurus Restoration.jpg

AMNH 6368 AMNH 6368 Therizinosaur.png

Nothronychus mckinleyi Nothronychus mckinleyi Restoration.png


Erlikosaurus Erlikosaurus Restoration.png


"Nanshiungosaurus" bohlini

Nothronychus graffami Nothronychus graffami Restoration.png



Life restoration of Erliansaurus in a sitting stance. Therizinosaurus may have sat on its pelvis during feeding

In 1993 Dale A. Russell and Donald E. Russell analyzed Therizinosaurus and Chalicotherium (species treated in this study is now regarded as Anisodon[32]) and noted similarities in their respective body plan, even though they form part of different groups. Both genera had large, well-developed, and relatively strong arms; the pelvic girdle was robust and suited for a sitting behavior; and the hindlimb (particularly the foot) structure was robust and shortened. They considered these adaptations to represent an example of convergent evolution—a condition where organisms evolve similar traits without necessarily being related—between extinct mammal and dinosaur genera. Moreover, this body plan is somewhat exhibited by the modern-day gorillas. Because the animals with this type of body plan are known to represent herbivores, the authors suggested this lifestyle for Therizinosaurus. Russell and Russell reconstructed the feeding behavior of Therizinosaurus as being able to sit while consuming foliage from large shrubs and trees. The plant material would have been harvested with its hands and this action was likely favored by its elongated neck which prevented the use of large amounts of force and effort. As its arms were long enough to have touched the ground during certain stances, they could have helped the dinosaur to rise from a prone position. If browsing in a bipedal stance, Therizinosaurus may have been able to reach even higher vegetation supported by its short and robust feet. Whereas Chalicotherium was more suited to hook branches, Therizinosaurus was better at pushing large clumps of foliage because of its long claws. It is also possible that Therizinosaurus was less capable of great precision in its movements than was Chalicotherium, due to the latter having more developed brain, dental and muscular capacities.[33]

Anthony R. Fiorillo and colleagues in 2018 suggested that Therizinosaurus had a reduced bite force that may have been useful for cropping vegetation or foraging, based on relative therizinosaurids such as Erlikosaurus and Segnosaurus. As the bite force started to decrease from primitive to derived therizinosaurians, Therizinosaurus, being a derived member, would have been subject to this evolutionary relationship.[34]

Arms and claws function[edit]

Lateral view of the unguals in specimens MPC-D 100/15, 100/16, and 100/17. Therizinosaurus may have used its claws for grasping foliage

When first described by Maleev in 1954, he considered that the unusually large claws were used to harvest seaweed. This was however, based on the assumption of a giant marine turtle.[1] In 1970, Rozhdestvensky re-examined the claws and suggested a possible function specialized in opening termite mounds or a frugivore diet.[2] Barsbold in 1976 suggested that the unusual claws of Therizinosaurus may have been employed to impale or dig up loose terrain, however, he pointed out their notorious fragility upon impact.[4] In 1995, Lev A. Nessov suggested the elongated claws were used for defense against predators and juveniles could have used their claws for arboreal locomotion, in a similar way to the modern-day sloths or hoatzin chicks.[35]

In 2014, Lautenschlager tested the function of various therizinosaur hand claws—including Therizinosaurus—through digital simulations. Three different functional scenarios were simulated for each claw morphology with a force of 400 N applied in each scenario: scratch/digging; hook-and-pull; and piercing. Though the stocky claws of Alxasaurus resulted in low-stress magnitudes, the stress was greater with the curvature and elongation of the claws in Falcarius, Nothronychus and Therizinosaurus. Some of the highest stress, deformation, and strain magnitudes were obtained in the scratch/digging scenario, the hook-and-pull scenario, in contrast, resulted in lower magnitudes, and lesser ones were found in the piercing scenario. Particularly, the overall stress was most pronounced in the unusual claws of Therizinosaurus, which may represent an exceptional case of elongation specialization. Lautenschlager noted the more strongly curved and elongate claws of some therizinosaurian taxa were poorly functional in a scratch/digging fashion, indicating this as the most unlikely function. Though fossorial (digging) behavior has been reported in several dinosaur species, the large body size largely rules out the possibility of burrow digging in therizinosaurs. Nevertheless, an overall digging action would have been done with the foot claws because, since as in other maniraptorans, feathers on the arms would have interfered with this function. Instead of being used for fossorial behavior, it is more likely that Therizinosaurus make use of its hands in a hook-and-pull fashion to pull or grasp vegetation within reach. This herbivorous behavior would make therizinosaurs mostly similar to the extant anteaters and the extinct ground sloths. Lautenschlager could neither confirm nor disregard that the hand claws could have been used for defense, intraspecific competition, stabilization by grasping tree trunks during high browsing, sexual dimorphism, or gripping mates during mating given the lack of more specimens. He clarified that there is no evidence that the long claws of Therizinosaurus would have been used in active defense or attack, however, it is possible that these appendages could have had some role when facing a threat, such as intimidation.[36]

Scott A. Lee and Zachary Richards in 2018 based on bending resistance measurements of several dinosaur humeri, found the humeri of carnosaur, therizinosaur, and tyrannosaur dinosaurs to be relatively resilient to stress. This increased ability to withstand stress supports the idea that Therizinosaurus and other therizinosaurians used their arms in a robust fashion that generated significant forces. They also suggested that the prominent claws of some members could have been used as a defense against predators and other various functions. Unlike the generally light and agile ornithomimosaurs who avoided predation with speed, Therizinosaurus and relatives relied on arms and claws to face threats.[37]


The Nemegt Formation may have had similar environments to those of the swampy Okavango Delta

The remains of Therizinosaurus have been found in the well-known Nemegt Formation of the Gobi Desert. Although this formation has never been dated radiometrically because of the discontinuity of exposures and absence of datable volcanic rock facies, the vertebrate fossil assemblage suggests an early Maastrichtian stage possibly between 70 million and 68 million years ago. The Nemegt Formation is separated into three informal members. The lower member is mainly composed by fluvial sediments, while middle and upper members consist of alluvial plain, paludal, lacustrine, and fluvial sedimentation.[38][39]

The environments that Therizinosaurus inhabited have been determined by the sedimentation across the formation, the δ13C level preserved on the tooth enamel of many herbivorous dinosaurs and the numerous petrified wood across the formation. They consisted of large meandering and braided rivers with extensive woodlands composed of large, enclosed, canopy-like forests of Araucarias that supported diverse herbivorous dinosaurs like Therizinosaurus. The climate of the formation was relatively temperate (mean annual temperatures between 7.6 and 8.7 °C), characterized by monsoons with cold, dry winters and hot, rainy summers with the addition of mean annual precipitations between 775 mmm and 835 mmm, a precipitation that was subject to prominent seasonal fluctuations.[39][40] The wet environments of the Nemegt Formation may have acted as an oasis-like area that attracted oviraptorids from arid neighbour localities such as the Barun Goyot Formation, as evidenced on the presence of Nemegtomaia in both regions.[41] It has been previously suggested that the Nemegt Formation may have been similar to the modern-day Okavango Delta, which is also composed of mesic (well-watered) surroundings.[42]

Life restoration of a Therizinosaurus pair along with a small group of Prenocephale, and Adasaurus

The paleofauna of the Nemegt Formation was diverse and rich, composed of other dinosaurs such as the alvarezsaurs Mononykus and Nemegtonykus; deinonychosaurs Adasaurus and Zanabazar; ornithomimosaurs Anserimimus and Gallimimus; oviraptorosaurs Avimimus, Rinchenia and Elmisaurus; tyrannosaurids Alioramus and possibly Bagaraatan; ankylosaurids Saichania and Tarchia; and pachycephalosaurids Homalocephale and Prenocephale. The Nemegt megafauna included the ornithomimosaur Deinocheirus; hadrosaurids Barsboldia and Saurolophus; titanosaurs Nemegtosaurus and Opisthocoelicaudia; and the apex predator Tarbosaurus.[43][41][44][45] Additional paleofauna includes birds like Judinornis or Teviornis; abundants freshwater ostracods at numerous localities; fish; terrestrial and aquatic turtles such as Mongolochelys and Nemegtemys; and the crocodylomorph Paralligator.[46][47][48][49]

As the sediments in which Therizinosaurus remains have been found are fluvial-based, it is suggested that it may have preferred to forage on riparian areas.[33] Therizinosaurus due to its prominent height and high-browsing lifestyle, was one of the tallest dinosaurs in the Nemegt Formation paleofauna. It probably had no significant competition with other herbivores over the foliage, however, a niche partitioning with the titanosaurs—also long-necked dinosaurs—of the formation could have occurred. If Therizinosaurus was a grazer, on the other hand, it would have competed with contemporary grazers such as Saurolophus. Although small predators like dromaeosaurids and troodontids did not represent a threat to Therizinosaurus, the only other predator rivaling in size was Tarbosaurus. Because of the greater height of Therizinosaurus, a large Tarbosaurus may have been not able to bite any higher than the thighs or belly of an adult standing Therizinosaurus. The elongated claws may have been useful for self-defense or to intimidate the predator during this situation.[16] It is also possible that Therizinosaurus competed for other various resources with Deinocheirus, Saurolophus, Nemegtosaurus and Opisthocoelicaudia.[42]

See also[edit]


  1. ^ a b c Maleev, E. A. (1954). "Новый черепахообразный ящер в Монголии" [New turtle like reptile in Mongolia]. Priroda (in Russian) (3): 106−108. Translated paper
  2. ^ a b c Rozhdestvensky, A. K. (1970). "О гигантских когтевых фалангах загадочных рептилий мезозоя" [On the giant claws of enigmatic Mesozoic reptiles]. Paleontological Journal (in Russian). 1970 (1): 131−141.
  3. ^ Osmólska, H.; Roniewicz, E. (1970). "Deinocheiridae, a new family of theropod dinosaurs" (PDF). Palaeontologica Polonica (21): 5−19.
  4. ^ a b c d e f g h i Barsbold, R. (1976). "Новые данные о теризинозавре (Therizinosauridae, Theropoda)" [New data on Therizinosaurus (Therizinosauridae, Theropoda)]. In Kramarenko, N. N.; Luvsandansan, B.; Voronin, Y. I.; Barsbold, R.; Rozhdestvensky, A. K.; Trofimov, B. A.; Reshetov, V. Y. (eds.). Paleontology and Biostratigraphy of Mongolia. The Joint Soviet-Mongolian Paleontological Expedition, Transactions (in Russian). Moscow: Nauka Press. pp. 76−92.
  5. ^ Gradziński, R.; Jaworowska, Z. K.; Maryańska, T. (1977). "Upper Cretaceous Djadokhta, Barun Goyot and Nemegt formations of Mongolia, including remarks on previous subdivisions". Acta Geologica Polonica. 27 (3): 281−326.
  6. ^ a b c Perle, A. (1982). "О находке задней конечности Therizinosaurus sp. из верхнего мела Монголии" [On a new finding of the hindlimb of Therizinosaurus sp. from the Late Cretaceous of Mongolia]. Problems in Mongolian Geology (in Russian). 5: 94−98. Translated paper
  7. ^ a b Barsbold, R.; Maryańska, T. (1990). "Saurischia Sedis Mutabilis: Segnosauria". In Weishampel, D. B.; Osmolska, H.; Dodson, P. (eds.). The Dinosauria (1st ed.). Berkeley: University of California Press. pp. 408−415. ISBN 9780520067271.
  8. ^ a b c d e f g Zanno, L. E. (2010). "A taxonomic and phylogenetic re-evaluation of Therizinosauria (Dinosauria: Maniraptora)". Journal of Systematic Palaeontology. 8 (4): 503−543. doi:10.1080/14772019.2010.488045. S2CID 53405097.
  9. ^ Holtz, T. R.; Rey, L. V. (2007). Dinosaurs: The Most Complete, Up-to-Date Encyclopedia for Dinosaur Lovers of All Ages. Random House. ISBN 9780375824197. Genus List for Holtz 2012 Weight Information
  10. ^ Paul, G. S. (2016). The Princeton Field Guide to Dinosaurs (2nd ed.). Princeton, New Jersey: Princeton University Press. pp. 162−168. ISBN 9780691167664.
  11. ^ Campione, N. E.; Evans, D. C. (2020). "The accuracy and precision of body mass estimation in non‐avian dinosaurs". Biological Reviews. 95 (6): 1759–1797. doi:10.1111/brv.12638. PMID 32869488. S2CID 221404013.
  12. ^ a b Molina-Pérez, R.; Larramendi, A. (2016). Dinosaur Facts and Figures: The Theropods and Other Dinosauriformes. Princeton: Princeton University Press. p. 270. doi:10.1515/9780691190594. ISBN 9788416641154. JSTOR j.cdb2hnszb.
  13. ^ Dimond, C. C.; Cabin, R. J.; Brooks, J. S. (2011). "Feathers, Dinosaurs, and Behavioral Cues: Defining the Visual Display Hypothesis for the Adaptive Function of Feathers in Non-Avian Theropods". BIOS. 82 (3): 58–63. doi:10.1893/011.082.0302. JSTOR 23033900. S2CID 98221211.
  14. ^ Lautenschlager, S.; Lawrence, M. W.; Perle, A.; Zanno, L. E.; Emily, J. R. (2014). "Cranial anatomy of Erlikosaurus andrewsi (Dinosauria, Therizinosauria): new insights based on digital reconstruction". Journal of Vertebrate Paleontology. 34 (6): 1263−1291. doi:10.1080/02724634.2014.874529.
  15. ^ a b Hedrick, B. P.; Zanno, L. E.; Wolfe, D. G.; Dodson, P. (2015). "The Slothful Claw: Osteology and Taphonomy of Nothronychus mckinleyi and N. graffami (Dinosauria: Theropoda) and Anatomical Considerations for Derived Therizinosaurids". PLOS ONE. 10 (6): e0129449. Bibcode:2015PLoSO..1029449H. doi:10.1371/journal.pone.0129449. PMC 4465624. PMID 26061728.
  16. ^ a b c Senter, P.; James, R. H. (2010). "Hip heights of the gigantic theropod dinosaurs Deinocheirus mirificus and Therizinosaurus cheloniformis, and implications for museum mounting and paleoecology" (PDF). Bulletin of Gunma Museum of Natural History (14): 1−10.
  17. ^ Taylor, M. P.; Wedel, M. J. (2013). "Why sauropods had long necks; and why giraffes have short necks". PeerJ. 1: e36. arXiv:1209.5439. Bibcode:2012arXiv1209.5439T. doi:10.7717/peerj.36. PMC 3628838. PMID 23638372.
  18. ^ a b c d e f Barsbold, R. (1983). "Хищные динозавры мела Монголии" [Carnivorous dinosaurs from the Cretaceous of Mongolia] (PDF). Transactions of the Joint Soviet-Mongolian Paleontological Expedition (in Russian). 19: 89. Translated paper
  19. ^ Perle, A. (1979). "Segnosauridae - новое семейство позднемеловых хищных динозавров Монголии" [Segnosauridae - a new family of theropods from the Late Cretaceous of Mongolia]. Transactions of the Joint Soviet-Mongolian Paleontological Expedition (in Russian). 8: 45−55. Translated paper
  20. ^ Barsbold, R.; Perle, A. (1980). "Segnosauria, a new suborder of carnivorous dinosaurs" (PDF). Acta Palaeontologica Polonica. 25 (2): 190−192.
  21. ^ Barsbold, R. (1983). "O ptich'ikh chertakh v stroyenii khishchnykh dinozavrov" [Avian features in the morphology of predatory dinosaurs]. Transactions of the Joint Soviet Mongolian Paleontological Expedition (in Russian). 24: 96−103. Translated paper
  22. ^ Paul, G. S. (1984). "The segnosaurian dinosaurs: relics of the prosauropod-ornithischian transition?". Journal of Vertebrate Paleontology. 4 (4): 507–515. doi:10.1080/02724634.1984.10012026. ISSN 0272-4634. JSTOR 4523011.
  23. ^ Paul, G. S. (1988). Predatory Dinosaurs of the World. New York: Simon & Schuster. pp. 185−283. ISBN 9780671619466.
  24. ^ Gauthier, J. (1986). "Saurischian monophyly and the origin of birds". Memoirs of the California Academy of Sciences. 8: 45.
  25. ^ Sereno, P. C. (1989). "Prosauropod monophyly and basal sauropodomorph phylogeny". Abstract of Papers. Forty-Ninth Annual Meeting Society of Vertebrate Paleontology. Journal of Vertebrate Paleontology. 9 (supp. 3). p. 39A. ISSN 0272-4634. JSTOR 4523276.
  26. ^ Norman, D. B. (1990). "Problematic Theropoda: Coelurosauria". In Weishampel, D. B.; Osmolska, H.; Dodson, P. (eds.). The Dinosauria (1st ed.). Berkeley: University of California Press. pp. 280−305. ISBN 9780520067271.
  27. ^ Russell, D. A.; Dong, Z. (1993). "The affinities of a new theropod from the Alxa Desert, Inner Mongolia, People's Republic of China". Canadian Journal of Earth Sciences. 30 (10): 2107−2127. Bibcode:1993CaJES..30.2107R. doi:10.1139/e93-183.
  28. ^ Clark, J. M.; Perle, A.; Norell, M. (1994). "The skull of Erlicosaurus andrewsi, a Late Cretaceous "Segnosaur" (Theropoda, Therizinosauridae) from Mongolia". American Museum Novitates. 3115: 1–39. hdl:2246/3712.
  29. ^ Russell, D. A. (1997). "Therizinosauria". In Currie, P. J.; Padian, K. (eds.). Encyclopedia of Dinosaurs. San Diego: Academic Press. pp. 729−730. ISBN 978-0-12-226810-6.
  30. ^ Xu, X.; Tang, Z.; Wang, X. A. (1999). "A therizinosauroid dinosaur with integumentary structures from China". Nature. 339 (6734): 350−354. Bibcode:1999Natur.399..350X. doi:10.1038/20670. S2CID 204993327.
  31. ^ Hartman, S.; Mortimer, M.; Wahl, W. R.; Lomax, D. R.; Lippincott, J.; Lovelace, D. M. (2019). "A new paravian dinosaur from the Late Jurassic of North America supports a late acquisition of avian flight". PeerJ. 7: e7247. doi:10.7717/peerj.7247. PMC 6626525. PMID 31333906.
  32. ^ Anquetin, J.; Antoine, P.-O.; Tassy, P. (2007). "Middle Miocene Chalicotheriinae (Mammalia, Perissodactyla) from France, with a discussion on chalicotheriine phylogeny". Zoological Journal of the Linnean Society. 151 (3): 577−608. doi:10.1111/j.1096-3642.2007.00327.x.
  33. ^ a b Russell, D. A.; Russell, D. E. (1993). "Mammal-Dinosaur Convergence". National Geographic Research & Exploration. 9 (1): 70−79. ISSN 8755-724X.
  34. ^ Fiorillo, A. R.; McCarthy, P. J.; Kobayashi, Y.; Tomsich, C. S.; Tykoski, R. S.; Lee, Y.-N.; Tanaka, T.; Noto, C. R. (2018). "An unusual association of hadrosaur and therizinosaur tracks within Late Cretaceous rocks of Denali National Park, Alaska". Scientific Reports. 8 (11706): 11706. Bibcode:2018NatSR...811706F. doi:10.1038/s41598-018-30110-8. PMC 6076232. PMID 30076347.
  35. ^ Nessov, L. A. (1995). Динозавры северной евразии: Новые данные о составе комплексов, экологии и палеобиогеографии [Dinosaurs of northern Eurasia: new data about assemblages, ecology, and paleobiogeography] (PDF) (in Russian). Saint Petersburg: Institute of Earth Crust, Saint Petersburg University. pp. 45−46. Translated paper
  36. ^ Lautenschlager, S. (2014). "Morphological and functional diversity in therizinosaur claws and the implications for theropod claw evolution". Proceedings of the Royal Society B. 28 (1785): 20140497. doi:10.1098/rspb.2014.0497. PMC 4024305. PMID 24807260.
  37. ^ Lee, S. A.; Richards, Z. (2018). "The Surprisingly Strong Arms of the Therizinosaur Dinosaurs". The Physics Teacher. 56 (7). doi:10.1119/1.5055323.
  38. ^ Funston, G. F.; Currie, P. J.; Eberth, D. A.; Ryan, M. J.; Chinzorig, T.; Demchig, B.; Longrich, N. R. (2016). "The first oviraptorosaur (Dinosauria: Theropoda) bonebed: evidence of gregarious behaviour in a maniraptoran theropod". Scientific Reports. 6 (35782). doi:10.1038/srep35782. PMC 5073311. PMID 27767062.
  39. ^ a b Eberth, D. A. (2018). "Stratigraphy and paleoenvironmental evolution of the dinosaur-rich Baruungoyot-Nemegt succession (Upper Cretaceous), Nemegt Basin, southern Mongolia". Palaeogeography, Palaeoclimatology, Palaeoecology. 494: 29−50. Bibcode:2018PPP...494...29E. doi:10.1016/j.palaeo.2017.11.018.
  40. ^ Owocki, K.; Kremer, B.; Cotte, M.; Bocherens, H. (2020). "Diet preferences and climate inferred from oxygen and carbon isotopes of tooth enamel of Tarbosaurus bataar (Nemegt Formation, Upper Cretaceous, Mongolia)". Palaeogeography, Palaeoclimatology, Palaeoecology. 537 (109190). Bibcode:2020PPP...537j9190O. doi:10.1016/j.palaeo.2019.05.012.
  41. ^ a b Funston, G. F.; Mendonca, S. E.; Currie, P. J.; Barsbold, R.; Barsbold, R. (2018). "Oviraptorosaur anatomy, diversity and ecology in the Nemegt Basin". Palaeogeography, Palaeoclimatology, Palaeoecology. 494: 101−120. Bibcode:2018PPP...494..101F. doi:10.1016/j.palaeo.2017.10.023.
  42. ^ a b Holtz, T. R. (2014). "Mystery of the horrible hands solved". Nature. 515 (7526): 203−205. Bibcode:2014Natur.515..203H. doi:10.1038/nature13930. PMID 25337885.
  43. ^ Weishampel, D. B.; Barrett, P. M.; Coria, R. A.; Loeuff, J. L.; Xing, X.; Xijin, Z.; Sahni, A.; Gomani, E. M. P. (2004). "Dinosaur Distribution". In Weishampel, D. B.; Dodson, P.; Osmolska, H. (eds.). The Dinosauria (2nd ed.). University of California Press. pp. 596–598. ISBN 0520242092.
  44. ^ Chinzorig, T.; Kobayashi, Y.; Tsogtbaatar, K.; Currie, P. J.; Takasaki, R.; Tanaka, T.; Iijima, M.; Barsbold, R. (2018). "Ornithomimosaurs from the Nemegt Formation of Mongolia: manus morphological variation and diversity". Palaeogeography, Palaeoclimatology, Palaeoecology. 494: 91−100. Bibcode:2018PPP...494...91C. doi:10.1016/j.palaeo.2017.10.031.
  45. ^ Fanti, F.; Bell, P. R.; Currie, P. J.; Tsogtbataar, K. (2020). "The Nemegt Basin — One of the best field laboratories for interpreting Late Cretaceous terrestrial ecosystems". Palaeogeography, Palaeoclimatology, Palaeoecology. 494: 1−4. doi:10.1016/j.palaeo.2017.07.014.
  46. ^ Szczechura, J. (1978). "Fresh-water ostracodes from the Nemegt Formation (Upper Cretaceous) of Mongolia" (PDF). Paleontologia Polonica. 38: 65−121.
  47. ^ Newbrey, M. G.; Brinkman, D. B.; Winkler, D. A.; Freedman, E. A.; Neuman, A. G.; Fowler, D. W.; Woodward, H. N. (2013). "Teleost centrum and jaw elements from the Upper Cretaceous Nemegt Formation (Campanian-Maastrichtian) of Mongolia and a re-identification of the fish centrum found with the theropod Raptorex kreigsteini". In Arratia, G.; Schultze, H.-S.; Wilson, M. V. H. (eds.). Mesozoic Fishes 5 – Global Diversity and Evolution. Verlag Dr. Friedrich Pfeil. pp. 291−303. ISBN 978-3-89937-159-8.
  48. ^ Danilov, I. G.; Hirayama, R.; Sukhanov, V. B.; Suzuki, S.; Watabe, M.; Vitek, N. S. (2014). "Cretaceous soft-shelled turtles (Trionychidae) of Mongolia: new diversity, records and a revision". Journal of Systematic Palaeontology. 12 (7): 799−832. doi:10.1080/14772019.2013.847870. S2CID 86304259.
  49. ^ Turner, A. H. (2015). "A Review of Shamosuchus and Paralligator (Crocodyliformes, Neosuchia) from the Cretaceous of Asia". PLOS ONE. 10 (2): e0118116. Bibcode:2015PLoSO..1018116T. doi:10.1371/journal.pone.0118116. PMC 4340866. PMID 25714338.

External links[edit]