Middle Pleistocene Pongo from Ganxian Cave in southern China with implications for understanding dental size evolution in orangutans

Fossil Pongo from the Early Pleistocene Gigantopithecus fauna of Chongzuo, Guangxi, southern China

The Boiano Basin is one of the largest Quaternary intermontane basins of the central‐southern Apennines within one of the most tectonically active areas of the Mediterranean region. In order to reconstruct its entire Quaternary stratigraphic, tectonic, and palaeoenvironment evolution, lithofacies and palaeomagnetic analyses have been performed on a 900 m‐deep borehole (CP1) drilled in the southwestern sector of the basin. The Quaternary succession consists of an alternating of alluvial fan and fluvial–marshy deposits for a total thickness of 240 m, unconformably laying on Lower Miocene deposits of the Sannio Unit, thrusted on upper Miocene deposits of the Molise Flysch. In addition, the stratigraphic study and facies distribution of 29 intermediate and shallow wells drilled in the basin, allowing us to define the thickness and lithofacies variations of the Quaternary sedimentary units inside the entire Boiano Basin in the sector of Campochiaro alluvial fan. Our results demonstrate that the Boiano Basin infilling started during the late Early Pleistocene (c. 1.1 Ma) and developed with variation in lithofacies distribution and thickness. The first depositional unit (Early Pleistocene–early Middle Pleistocene in age) was palustrine and fluvial–marshy, the second (Middle Pleistocene in age) was characterized by the occurrence of the first cycle of alluvial fan deposition, the third (late Middle Pleistocene in age) was newly palustrine and fluvial marshy and, finally, the fourth recorded two cycles of alluvial fan deposition (late Middle Pleistocene and Late Pleistocene in age, respectively), interspersed by short periods of palustrinity, tephra layers deposition, and palaeosols development. The study allows the hypothesizing that the Quaternary infilling was accommodated within a graben (or semigraben) structure, affected mainly by extensional fault systems localized in the inner part of the basin and secondly by fault systems bounding the basin.

The Middle and Late Pleistocene mammalian faunas of Japan are described with new opinions on their succession and relation to the continental faunas. Although fossil materials assignable to early Middle Pleistocene are seemingly scarce in Japan, the fauna of that time is considered to have been transitional between the Early and Middle Pleistocene ones. On the other hand, fossil records which are younger than early Middle Pleistocene are abundant from the mainlands of Japan; viz. the Honshu-Shikoku-Kyushu area.In the middle Middle Pleistocene, the fauna of this area contained a considerable number of taxa which are extant today in the area (about 50%). It was also characterized by a high proportion of endemic species and the predominance of temperate forest elements. From this time to the late Middle Pleistocene, several species disappeared from the fauna; at the same time, immigrants from the continent were scarce. The faunal characters of the late Middle Pleistocene were basically identical with those of the preceding time.In the early Late Pleistocene, no mammal seems to have immigrated from the neighboring continent, and faunal composition was almost consistent with that of the late Middle Pleistocene. The elements of that fauna still persisted in the late Late Pleistocene, apart from the extinction of a few forms. In addition to the fact mentioned above, immigration from the northern part of the continent was recognized in the late Late Pleistocene, although it was restricted to a few large herbivore forms and to a short time duration.The introduction of the continental faunas to the mainlands of Japan during Middle and Late Pleistocene times was not so remarkable as previously inferred. Therefore it becomes doubtful that the faunas of the area were drastically replaced by the immigration of the Choukoutien, Wanhsien and Loess faunas of China during those times.

New Light on the Earliest Hominid Occupation in East Asia

Evolutionary trend in dental size in fossil orangutans from the Pleistocene of Chongzuo, Guangxi, southern China

Hominin distribution and density patterns in Pleistocene China: Climatic influences

A reappraisal of the Early to Middle Pleistocene Italian Bovidae

The current study focuses on the emblematic Myopus/Lemmus species complex (tribe Lemmini) in the European Pleistocene fossil record. The members of the two genera occupy distinct ecological niches and have different external appearances, but they are remarkably similar in their dental morphology, so that they were commonly thought of as undistinguishable in the fossil record. Thus, more or less all European Lemmini fossils have been assigned to the genus Lemmus. In the Early Pleistocene site of Schernfeld (Germany), the species Lemmus kowalskii had been described. It was thought by some authors that all Lemmini from Early to late Middle Pleistocene belong to this species.In the current study, we investigated Lemmini molar morphology from Western and Central European sites including Schernfeld (Early Pleistocene), Sackdillinger Höhle (Sackdilling Cave), and Koněprusy C718 (both early Middle Pleistocene), as well as other fossil localities with fewer specimens, formerly assigned to Lemmus kowalskii. Using an extensive modern referential material of Lemmus and Myopus, this study proposes to re-evaluate taxonomic status of the Middle and Early Pleistocene Lemmini. This modern referential also allows a better understanding of the morphology of Lemmus kowalskii specimens and its variability.Our results highlight the very high variation within fossil populations, as well as significant statistical differences between populations of the Early and Middle Pleistocene localities. A large part of these fossil specimens is firmly identified as Myopus sp., including the L. kowalskii holotype. Our identifications demonstrate that in most Early and Middle Pleistocene sites considered in this study, both genera (Lemmus and Myopus) are present. Possible interpretations and consequences for current view of lemming history are discussed, as well as some of the paleoecological and paleoenvironmental implications.

Taxonomical revision of fossil Canis in Middle Pleistocene sites of Zhoukoudian, Beijing, China and a review of fossil records of Canis mosbachensis variabilis in China

Ecological transitions — But for whom? A perspective from the Pleistocene

Quaternary marine transgressions in eastern China

On the basis of the results of former studies by the present authors five main groups of bears are recognized: Ursus gr. minimus - thibetanus (black bears), Ursus gr. etruscus (etruscan bears), Ursus gr. arctos (brown bears), Ursus gr. deningei - spelaeus (cave bears) and Ursus gr. maritimus (white bears). Black bears seem to have disappeared from Europe during the Late Pliocene, immigrated again at the beginning of the Middle Pleistocene, and definitively died out in Europe at the beginning of the Late Pleistocene. Etruscan bears occur more or less contemporaneously in the southern areas of Europe and Asia during the Late Pliocene. The Asian branch apparently became extinct at the end of this period, while the European stock survived, giving rise to more advanced representatives during the Early Pleistocene. Brown bears seem to have originated in Asia. This group dispersed widely in holoarctic areas diversifying into a great number of varieties. They reached Europe presumably at the very end of the Early Pleistocene. The arrival of brown bears in Europe is a crucial event, which approximately coincides with the great faunal turnover which marks the Early-Middle Pleistocene transition. Brown bears replaced the etruscan bears, typical of the Villafranchian faunal assemblages, and gave rise to the cave bear line. Cave bears were very successful in Europe during the Middle and Late Pleistocene and disappeared at the end of the last glaciation or even at the very beginning of the Holocene. White bears presumably originated from northern Eurasian brown bear populations during the Late Pleistocene.

Hominin diversity in East Asia during the Middle Pleistocene: A premolar endostructural perspective

Biostratigraphic correlation of Pleistocene marine deposits and sea levels, Atlantic coastal plain of the southeastern United States

<p>The trend of giant panda (<i>Ailuropoda</i>, Ursidae) body size evolution during the Quaternary has long been observed primarily through dental size analysis. However, exact body mass estimations have been lacking, whereas the dental size is generally viewed as a poor index for body mass estimation. In this study, we assess the accuracy of body mass prediction based on dentition using data from extensive cranial, dental, and postcranial fossil remains recovered in the Shuanghe Cave, Guizhou, southwestern China. Our results support a high degree of accuracy in body mass estimation based on m1 length, likely due to the relatively stable proportion of this tooth to the whole body in the Quaternary <i>Ailuropoda</i>. Our analyses of the body mass evolution of giant pandas since the earliest Pleistocene reveal rapid growth in body mass from <i>A. microta</i> to <i>A. melanoleuca</i> in the Early Pleistocene. This was followed by an initial increase and subsequent decrease in body mass, leading to the modern form since the Middle Pleistocene. The initial period of rapid growth is likely driven by the increasing feeding efficiency on bamboo, facilitating larger body sizes. In contrast, the later fluctuation in body mass coincides with climatic and monsoon change in the Middle and Late Pleistocene, directly impacting bamboo availability. The body mass evolution of the giant panda offers insights into its historical adaptation, highlighting the correlation of evolution and paleoclimatic change during the Quaternary.</p>