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Neochoristodera
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Neochoristodera is a lineage of specialised -like fully aquatic . Noted for their long jaws and large size, these animals were predominant across the Northern Hemisphere, occurring in freshwater and coastal environments across the and early .


Systematics
Neochoristoderes form a monophyletic group, however there is no consensus about the relationships of the genera, which have been recovered as a in recent studies. Neochoristodera contains the named genera , , , , , and . Various taxa of uncertain affinities within this group are known, including a partial femur of a choristodere, possibly of a neochoristodere from the Cedar Mountain Formation of the United States and an indeterminate partial skeleton from the Kuwajima Formation of Japan.Matsumoto, R., Manabe, M., & Evans, S. E. (2015). The first record of a long-snouted choristodere (Reptilia, Diapsida) from the Early Cretaceous of Ishikawa Prefecture, Japan. Historical Biology 27(5):1-12.


Evolution
Neochoristoderes first appear in the of , where they co-exist with other choristodere groups like and . Here, a regional absence of aquatic , possibly due to colder temperatures, seems to have opened the ecological niche for these choristoderes to occupy a similar ecological niche.R. Matsumoto and S. E. Evans. 2010. Choristoderes and the freshwater assemblages of Laurasia. Journal of Iberian Geology 36(2):253-274 The oldest known neochoristodere is , from the - aged Mengyin Formation of China.

Other than a possible specimen from the Cedar Mountain Formation, a large gap occurs between these Early Cretaceous faunas and the Late Cretaceous ones. There are no fossils of neochoristoderes in the Asian Late Cretaceous, but the subsequent distribution of in the and implies that there were Asian taxa around this time, seeing as Simoedosauridae is predominantly Asian and only propagated widely after the KT event.

Choristoderes reappear in the fossil record in the of under the genus . This genus survives the KT event unscathed and diversifies in the aftermath, being soon after joined by . Both taxa remain at high latitudes in and until the Eocene, when they mysteriously disappear.

In 2021, fossil remains of indetermine neochoristoderes were described from several sites from the Navesink Formation and Marshalltown Formation (Ellisdale Fossil Site) of , marking the first known occurrence of neochoristoderes from the former landmass Appalachia. Niche modeling based on the presumed niche of Champsosaurus indicates that neochoristoderes may have had a widespread distribution in Appalachia, but the majority of this habitat was not located in areas conducive for Cretaceous fossilization, leading to only a small margin of optimal habitat in New Jersey that preserved choristodere remains.

Competition from has been at times implicated in the extinction of neochoristoderes. There appears to be a niche partitioning between neochoristoderes and long-snouted crocodilians such as , which are absent from freshwater sites in Laurasia until well after neochoristoderes disappear, but competition between both groups, if it even existed, is currently unaccounted for. Ultimately, both and co-existed with a variety of broad-snouted species like and .


Biology
Neochoristoderes are thought to be fully aquatic. They possess laterally flattened, muscular tails and paddle-like limbs, their torsos are dorsoventrally flattened with short but massive ribs and their are heavily ossified, facilitating sinking. While they have their nostrils at the end of the snout as in crocodiles, they are oriented towards the tip instead of dorsally; their eye sockets are similarly forward-facing, implying that these animals did not surface often and probably simply rose the snout in a snorkel-like fashion. As in most choristoderes the skin lacks , instead having small, non-overlapping scales. In adult females are thought to have particularly ossified limbs and pelvises, implying that they could crawl unto land, while adult males and juveniles could not.Katsura, Yoshihiro. (2007). Fusion of sacrals and anatomy in Champsosaurus (Diapsida, Choristodera). Historical Biology, 19(3), 263-271, As most choristoderes are thought to have been or , it is likely that at least some neochoristoderes were too.

Most neochoristoderes have exceptionally large temporal fenestrae, suggesting powerful bite forces; is estimated to have a bite force around 1194 to 1910 N, as opposed to the modern 's 310-497 N.James, M. (2010). The jaw adductor muscles of Champsosaurus and their implications for feeding mechanics. Master’s. University of Alberta Education and Research Archive. In spite of this, most are thought to have had a diet similar to that of modern gharials due to the long and slender jaws, though has a more robust and shorter snout and could have fed on larger prey.

Compared with other choristoderes, which have rather simple teeth, neochoristoderes have teeth completely enveloped in striated with an enamel infolding at the base, labiolingually compressed and hooked, the exception being which has still rather simple teeth aside from the start of an enamel infolding. There is some tooth differentiation, with the anterior teeth being larger than the posterior ones. As with most choristoderes, neochoristoderes have palatal teeth, indicating food manipulation in the mouth.Matsumoto, R., & Evans, S. E. (2016). Morphology and function of the palatal dentition in Choristodera. Journal of Anatomy, 228(3), 414-429.

Nearly all neochoristodere remains occur at high latitudes, suggesting a preference for temperate climates. fossils are known in the and .

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