分类： 生物学 >> 生物进化论 提交时间： 2024-03-15
摘要： All the extant rhino species belong to Rhinocerotini and either have one horn (a nasal horn) or two horns (a nasal horn and frontal horn). So far, the earliest Rhinocerotini to have been identified in China is the “Dicerorhinus” cixianensis, which was based on a juvenile skull with an associated mandible from the Middle Miocene locality of Jiulongkou in Cixian County, HebeiProvince of northern China. Our analyses suggest that there are similarities between this specimenand the modern genus, Dicerorhinus, but it differs in several cranial traits and therefore cannotbe assigned to the modern genus. Instead, it is closer to the Middle Miocene Lartetotheriumfrom Europe, especially the specimen from La Retama in Spain and should be assigned to thatgenus, indicating the presence of intracontinental dispersal at this time. The Jiulongkou faunais the only Middle Miocene fauna with Rhinocerotini in China, and, together with the faunalcomposition, this implies a more humid and closed environment, in contrast to those found inwestern China. We suggest that the position of the posterior border of the nasal notch is a goodindication of the specimen’s evolutionary level in Rhinocerotini. The anterior position of the nasalnotch as seen in modern Dicerorhinus, together with its certain similarities to L. cixianensis aswell as its differences with more specialized species of the Dihoplus-Pliorhinus-Stephanorhinus-Coelodonta lineage, supports the conclusion that Dicerorhinus experienced little change during anearly 10 Myr evolutionary history, possibly due to the low selection pressure seen in the tropical/subtropical forests in southeastern Asia.
分类： 生物学 >> 动物学 提交时间： 2020-03-31 合作期刊: 《古脊椎动物学报》
摘要： The elephantimorph proboscideans, Serridentinus gobiensis Osborn & Granger, 1932, and Miomastodon tongxinensis Chen, 1978, from the Middle Miocene of northern China, were revised as Zygolophodon gobiensis (Osborn & Granger, 1932). However, their phylogenetic positions are still being debated because of their intermediate morphology between the typical bunodont (Gomphotheriidae) and zygodont (Mammutidae) elephantimorphs. In the present paper, we compare their dental and mandibular morphology with that of the Eurasian Z. turicensis, Gomphotherium subtapiroideum, and G. tassyi, as well as the North American Mio. merriami and G. productum. It appears that S. gobiensis and Mio. tongxinensis share with Mio. merriami the slightly more bunodont molar morphology than that of Z. turicensis, e.g., the thicker enamel, thicker pretrite crescentoids, higher interlophid enamel pillars in buccal view, and the narrower contour majorly caused by the narrower posttrite half loph(id)s. S. gobiensis and Mio. merriami also possess an “erected oval cross-sectioned mandibular tusk”, in which the cross-section is mediolaterally compressed (dorsoventral diameter being larger than the mediolateral one). Whereas, in Z. turicensis and G. productum, the mandibular tusk is “laid oval cross-sectioned”, in which the cross-section is dorsoventrally compressed (dorsoventral diameter is smaller than the mediolateral one). Therefore, it is reasonable to revive the genus Miomastodon Osborn, 1922, which contains the species that were previously attributed to Zygolophodon, but they have relatively bunodont molar morphology (i.e., the robust type of the Z. turicensis group). The mandibular tusk with erected oval cross-section seems to be a synapomorphy of Miomastodon species. Furthermore, the molar morphology of G. subtapiroideum and G. tassyi also exhibits intermediate status between the typical bunodonts and zygodonts. However, the mandibular symphysis of G. subtapiroideum and G. tassyi is stronger than that of Miomastodon, and the mandibular tusk is pyriform cross-sectioned. The validity of Miomastodon and G. subtapiroideum/tassyi obscures the boundary between the Gomphotheriidae and Mammutidae, and suggests that the evolutions of the Gomphotheriidae and Mammutidae are deeply involved in with each other, rather than straightforwardly detached. This phenomenon has been revealed by a collagen sequence analysis among Notiomastodon, Mammut, and extant elephants, which should be further studied.
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