Dakotaraptor

, Rocky Mountain Dinosaur Resource Center In 2005, paleontologist Robert DePalma in Harding County, South Dakota discovered a fluvial bonebed bearing the remains of a variety of dinosaurian and non-dinosaurian remains, which yielded a partial skeleton attributed by DePalma to a large dromaeosaurid. Subsequently, the same site produced additional dromaeosaurid remains. In 2015, the type species Dakotaraptor steini was named and described by Robert A. DePalma, David A. Burnham, Larry Dean Martin, Peter Lars Larson, and Robert Thomas Bakker. The generic name, Dakotaraptor, combines a reference to South Dakota and the Dakota people with the Latin word raptor, meaning "plunderer". The specific name, steini, honors paleontologist Walter W. Stein. Dakotaraptor was one of eighteen dinosaur taxa from 2015 to be described in open access or free-to-read journals. The holotype, PBMNH.P.10.113.T, was found in a sandstone layer of the upper Hell Creek Formation, dating to the late Maastrichtian. It consists of a partial skeleton of an adult individual, albeit without a skull. It contains a piece of a back vertebra, ten tail vertebrae, both humeri, both ulnae, both radii, the first and second right metacarpals, three claws of the left hand, a right thighbone, both shinbones, a left astragalus bone, a left calcaneum, the left second, third and fourth metatarsal, the right fourth metatarsal, and the second and third claw of the right foot. An assigned furcula was later excluded from the specimen. In 2016, DePalma et al. recognized that none of the referred furculae actually belonged to Dakotaraptor and excluded them from its hypodigm. In 2024, even the dinosaurian elements of Dakotaraptor were questioned, with supposed traits diagnostic for dromaeosaurs also referrable to caenagnathids and ornithomimosaurians. ==Description==

Size , Velociraptor'' and a human Dakotaraptor is exceptionally large for a dromaeosaurid, with an estimated adult length of . This approaches the size of one of the largest known dromaeosaurids, Utahraptor. Dakotaraptor, however, does not have the proportions and adaptations of Utahraptor, but more closely resembles smaller dromaeosaurids, like Deinonychus. Distinguishing traits Apart from its large size, the description of 2015 indicated some additional distinguishing traits. On the fourth foot claw, the boss that serves as an attachment for the tendon of the flexor muscle is reduced in size. The "blood groove" on the outer side of the fourth claw of the foot, towards the tip, is fully enclosed over half of its length, forming a bony tubular structure. The second and third claws of the foot have sharp keels at their undersides. The second foot claw, the "sickle claw", equals 29% of the thighbone length. On the shinbone, the crista fibularis, the crest that contacts the calfbone, is long and lightly built, with a height that does not exceed 9% of the crest length. The upper edge of this crest ends in a hook. On the second metacarpal, of the two condyles that contact the finger, the inner one is almost as large as the outer one. The outer side of the second metacarpal has but a shallow groove for the ligament that connects it to the third metacarpal. When the arm is seen in a flat position, of the second metacarpal, the edge between the wrist joint and the upper shaft is straight in top view. The teeth have fifteen to twenty denticles per on the rear edges and twenty to twenty-seven denticles on the front edges. Skeleton Vertebral column The vertebrae of the back are highly pneumatised, filled with trabecular bone that shows many air spaces. On the middle tail vertebrae, the front joint processes, the prezygapophyses, are extremely elongated with an estimated intact length of , spanning about ten vertebrae. This helps to stiffen out the tail. Arms The wing of Dakotaraptor was given much attention in the describing article. Here, "wing" is used as an anatomical descriptive term not related to its functionality, since Dakotaraptor was flightless. This is similar to the term "wing" for the same appendages in ostriches, emus, and other flightless birds. It is meant to express that the arm is equipped with long feathers resembling those of flight feathers in birds that can actually fly. Many of the wing bones were discovered (humerus, radius, ulna, two of the three metacarpal wrist bones, and parts of the finger digits), so the wing is very complete. The humerus, the upper arm bone, is relatively long, slender, and somewhat bent to the inside. The most notable anatomical feature is the row of very prominent bumps along a ridge on the lower edge of the ulna, one of the forearm bones. These are called ulnar papillae, more commonly known as quill knobs. In birds and some other theropod dinosaurs, these bumps were spots for reinforced attachment of the remiges, or wing feathers. When quill knobs are present, this is considered a strong indication that the animal had long remiges on the wings. Since quill knobs are rare in the fossil record, paleontologists mainly relied on phylogenetic bracketing to determine if a species was likely to have had wing feathers - if a relative on a "higher" branch of the evolutionary tree had the feathers and one on a "lower" down branch had them too, then a species in the middle position likely did as well. Dakotaraptor’s quill knobs show that the animal unequivocally had prominent wing feathers, making it the largest dromaeosaurid with confirmed plumage of that type. The quill knobs of Dakotaraptor have a diameter of about , which shows that these feathers were rather large. It was estimated that a complete series might include fifteen of these papillae ulnares. The ulna is long and the other lower arm bone, the radius, measures . The hand bones show that their joints allowed for little mobility. The wingspan of Dakotaraptor was estimated at , not taking into account possible primary remiges longer than the hand. The second metacarpal of the metacarpus of the hand, the bone that primary remiges attach to, also had a flat bony shelf as its dorsal surface. The shelf made a perfect spot for the primary feathers to lay across in their life-attachment. Legs Overall, the legs of Dakotaraptor are lightly built and have long elements, contrary to the robust, stocky legs of Utahraptor. Dakotaraptor more closely resembles the agile, springy smaller dromaeosaurids and would have been well-suited to running and pursuit predation. The length of the thighbone is . It is relatively shorter and more lightly built than that of Utahraptor. On the contrary, the shinbone is rather elongated. The holotype shinbone is, with a length of , the longest dromaeosaurid tibia known. It is 22% longer than the thighbone, indicating high running capability. The shinbone's cnemial crest has a sharp corner pointing to the front. Its fibular crest ends in a hook-shaped process pointing up, a condition that is unique in the entirety of Theropoda. The astragalus and calcaneum, the upper ankle bones, are fused and similar to those in Bambiraptor. The top of the calcaneum has but a small contact facet for the calfbone, indicating that this fibula must have had a very narrow lower end. The metatarsus has an estimated length of , which makes it rather long when compared to the remainder of the leg. The foot claws of Dakotaraptor include a typical dromaeosaurid raptorial second claw, or "sickle claw", which was used for killing or holding down prey. It is large and robust with a diameter of and a length of measured along the outer curve. This equals 29% of the length of the thighbone (as previously mentioned), compared to 23% in Deinonychus. The claw is transversely flattened and has a droplet-shaped cross-section. The flexor tubercle, a large bump near the base, served as an attachment site for flexor muscles - the larger it was, the greater the slashing strength. Dakotaraptor has a flexor tubercle that is larger relative to overall claw size than it is in other discovered dromaeosaurids, potentially giving it the strongest slashing strength of any known member of this group. The flexor tubercle on the third claw of the foot is almost non-existent, being very reduced in size compared to other dromaeosaurids. This suggests a more minimized use of that claw. As these are the bony cores of the claws, they would have been covered in a keratinous sheath that extended the "nail" and ended in a sharp tip. The third claw is keeled too, but is much smaller, with a tip to joint length of and a curve length of . The groove on its outer side towards the tip ends in a bone tunnel, which is a rare condition. ==Classification==

Dakotaraptor was placed in Dromaeosauridae. A cladistic analysis showed that it was the sister taxa of Dromaeosaurus. They again formed a clade with Utahraptor, of which clade Achillobator was the direct side branch. Despite being related to other large dromaeosaurids, Dakotaraptor was suggested to represent a separate fourth instance of dromaeosaurid size increase, besides Deinonychus, Unenlagia, and the Achillobator plus Utahraptor clade. If this study proves correct, then Dakotaraptor would have been one of the northernmost genera of Unenlagiine known. In the recently performed phylogenetic analysis by Currie and Evans in 2019, Dakotaraptor was again recovered as an eudromaeosaur, though the authors noted that the holotype may not represent one individual. }} In their description of Dineobellator, Jasinski et al. (2020) (using the same dataset as Currie and Evans (2019)) again recovered this position for Dakotaraptor, but also noted the likely status of Dakotaraptor as a chimaera, casting doubt on this placement as too basal because of the potential composite nature of the taxon. Teeth are the only overlapping features between Acheroraptor and Dakotaraptor. However Acheroraptor is significantly smaller and differs from Dakotaraptor only in that it possesses vertical ridges on the tooth crowns. ==Paleobiology==

'' is the victim. The keeled claw of the second toe, the "sickle claw", was used to bring down prey and had a more robust flexor tubercle than that of Utahraptor. On the contrary, the third foot claw was relatively smaller in size than with other dromaeosaurids and seems not to have had an important function in attacking prey. Two morphs, a robust one and a gracile one, were present in the fossil material. A study of the bone histology showed that both morphs were adults, so the lighter build of some bones was not caused by a young age. Individual variety or pathologies might account for the difference, but the simplest explanation is sexual dimorphism. It can as yet not be deduced which morph was male and which morph was female. On the ulna of the lower arm, wide quill knobs are present, attachment points for large pennaceous feathers (as previously mentioned). Adult Dakotaraptor individuals were much too heavy to fly. Despite this flightless condition, the feathers were not reduced. There is a variety of possible alternative functions for its wings, including shielding of eggs, display, intimidation, and keeping balance while pinning down prey with the sickle claw. These functions, however, do not necessitate quill knobs and the describing authors considered it likely that Dakotaraptor descended from a smaller flying ancestor that had them. ==Paleoecology==

of the Hell Creek Formation (Dakotaraptor in caramel brown) Dakotaraptor is the second medium-sized predator discovered in the Hell Creek Formation after Nanotyrannus, intermediate in length between the giant tyrannosaurid Tyrannosaurus and smaller deinonychosaurians, like Acheroraptor. ==Notes==