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Lotheridium is an extinct genus of that lived in what is now Asia during the Late Cretaceous, about 72–66 million years ago. The genus contains a monotypic taxon, Lotheridium mengi, named in 2015 after paleontologist Jin Meng. It is known from a single fossil specimen—a skull with associated lower jaws—found in the Qiupa Formation of Henan Province, China and housed in the collections of the Zhejiang Museum of Natural History. The skull measures in length, suggesting Lotheridium was large compared to most other deltatheroidans. Though the preserved skull is almost complete, it has been flattened and the skull roof was crushed during fossilization.
Lotheridium is believed to be a carnivore. It had a short snout and 46 teeth, among which the upper Canine tooth are the largest and most elongated. Though its lower canines are far smaller than the upper pair, they are still large enough that there are small gaps in the upper jaw to hold them when the mouth is closed. Its molars are adapted for shearing flesh. They bear unique cusps which can be used to differentiate it from its relatives. As with all deltatheroidans, its closest living relatives are the .
As the first deltatheroidan found in central China, Lotheridium showed that the group was more widespread across Asia than previously known. Deltatheroidans are otherwise known from North American adn elsewhere in Asia, and debate exists over which continent the group first evolved in before spreading the other. Dating to the Maastrichtian age, the Qiupa Formation represents a tropical to subtropical depositional environment with a shallow lake and braided river delta. Lotheridium lived alongside a many different species such as dinosaurs, lizards, turtles, and other mammals.
snout of Lotheridium is short and makes up under a third of the skull's length. The short premaxilla bone forms the tip of the upper jaw and bears all the upper incisor teeth, in addition to forming the front margin of the socket for the upper canine tooth. This bone has a large indentation between where the canine and hindmost incisor are positioned, which the tip of the lower canine fits into when the mouth is shut. Most of the incisive foramen (an opening on the hard palate) is also present on the premaxilla. The hind margin of this foramen is on the maxilla bone, as is most of the upper canine socket. This bone has a large opening called the infraorbital foramen, in front of which the maxilla depresses inward, possibly to serve as an attachment point for facial muscles. Behind the maxilla is the lacrimal bone, located behind the eye socket and expanding greatly onto the face. The middle of the skull roof is made up of the , and the hind part of the roof is formed by the larger . Each frontal bears a bony projection called a postorbital process and a ridge behind it called the temporal line. These ridges converge towards the back of the bone and join each other at the border of the frontal and parietal bones, forming a sagittal crest. The cheek bones are strongly arched, forming a structure known as the zygomatic arch on each side of the skull. The arch is mostly made up of a bone called the Jugal bone (though the lacrimal and Squamosal bone bones also contribute to it), which has a projection halfway down its length marking the back of the eye socket. At the hind part of each zygomatic arch is a depression called the mandibular fossa (where the lower jaw articulates), and behind this depression is a bony projection called the postglenoid process. Forming the middle of the underside of the skull is a wide, flat bone called the basisphenoid, with raised ridges on either side of it. Behind it is the basioccipital bone, which makes up the base of the skull and has a V-shaped indentation at its hind part. On either side of the notch is a large, rounded protrusion called an occipital condyle. Part of the middle ear is housed by a hollow, bulging protrusion of the petrosal bone called a promontorium, which bears a groove for a facial nerve and an oval window that opens to the side. Like that of the related Deltatheridium, the promontorium of Lotheridium has no grooves for blood vessels. The supraoccipital bone at the back of the skull has a prominent, backward-pointing structure called a lambdoidal crest.
The robust mandible (lower jaw) is deepest at the point where the third molar tooth is attached, and its underside is slightly curved. Two small openings called mental foramina can be seen from the side of the jaw, located below the first molar and second premolar teeth respectively. The coronoid process of the mandible (a projection behind the teeth) is prominent, its front margin forming a 135° angle with the corresponding tooth row. A depression where the masseter muscle would attach (known as the masseteric fossa) is visible below it. The point where the jaw articulates with the rest of the skull, called the mandibular condyle, is low and almost level with the teeth. On the lingual side of the mandible (the surfaces facing the tongue), the mandibular symphysis (where the two halves of the lower jaw join together) is unfused and an inward-facing bony projection is present at each angle.
Like other derived mammals, Lotheridium has a dental formula of for a total of 46 teeth. That is, each half of the upper jaw bears four incisors, one canine, three premolars and four molars, whereas each half of the lower jaw has three incisors, one canine, three premolars and four molars. The upper canines are very elongated, measuring and pointing downwards almost perpendicular to the jaw. Though not nearly as large as the upper canines, the lower canines are still tall compared to the rest of the teeth, and a small gap is present between the incisors and canines in each half of the upper jaw to accommodate the corresponding lower canine. Each of the upper premolars is separated from the one next to it by a small gap, as are the first and second lower premolars.
The first upper premolar of Lotheridium differs from those of some other extinct metatherians (namely the stagodontids Didelphodon, Eobrasilia and Eodelphis) in lacking a developed pair of accessory cusps. Furthermore, this tooth is proportionately larger in Lotheridium than it is in the aforementioned stagodontids, Malleodectes, Gaylordia, or Didelphopsis. Because the amount of wear on each molar decreases towards the back of the mouth in both the upper and lower jaws, it has been determined that the molars erupt in order from front to back. Unlike in all other deltatheroidans, the (one of the cusps) on the upper molars of Lotheridium stretch further sideways and the lower molars bear small cusps with a shelf-like structure (named "cuspule f"), so these features are used as the to distinguish Lotheridium from its relatives.
The pattern of deltatheroidan dispersal has been debated among experts. Historically, the group was believed to have first evolved in Asia and later spread into North America. This was because the former continent has yielded most of their known specimens, including some of the oldest known at the time (Coniacian-aged fossils of Sulestes from Uzbekistan). However, North American fossils of Atokatheridium and Oklatheridium which predate any known Asian deltatheroidans were later reported in the 2000s, leading some authors to believe that the group originated here. Even so, others continued to believe in an Asian origin for deltatheroidans, citing how Asian genera tend to be recovered in more basal (earlier-diverging) positions in phylogenetic analyses. Being one of the geologically youngest deltatheroidans, Lotheridium does not provide new information on the origins of the group, but its discovery in central China (where deltatheroidans had not been found previously) does show that the group was more widespread in Asia than formerly known.
Based on the amount of wear, the third premolar of both the upper and lower jaws in the only known Lotheridium specimen likely erupted far later than the first and second premolars. In extant marsupials (the closest living relatives of deltatheroidans), only the third Deciduous teeth premolar is replaced by a permanent tooth, whereas the first two are kept throughout the animal's life without replacement. The wear patterns indicate that Lotheridium had the same tooth replacement pattern as marsupials, and that this pattern had already evolved in the common ancestor of marsupials and deltatheroidans. This further suggests that the two groups may have similar feeding systems and reproductive patterns.
The deposits of the Qiupa Formation have yielded fossilized remains of a wide variety of animals which likely lived alongside Lotheridium. Remains of one other mammal species, the large multituberculate Yubaatar zhongyuanensis, have been discovered at this site. Dinosaurs are the most diverse animal group represented in the fossil assemblage of the formation, with the first to be discovered being teeth of a tyrannosaurid originally named as Tyrannosaurus luanchuanensis (sometimes considered a junior synonym of Tarbosaurus bataar). Smaller theropod dinosaurs have also been named from the Qiupa Formation, including the dromaeosaurid Luanchuanraptor, the oviraptorid Yulong mini, the ornithomimid Qiupalong, the alvarezsaurid Qiupanykus, and the enantiornithine bird Yuornis. Partial remains of sauropods, ankylosaurs and possibly protoceratopsids are also known, but have not been attributed to any named genera or species. Aside from dinosaurs, reptiles known from the Qiupa Formation fossil assemblage include the lizards Funiusaurus, Tianyusaurus, and Zhongyuanxi, as well as unnamed turtles.
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