In the southwestern Sulaiman geological province (Balochistan, Pakistan), terrestrial detrital facies from the Bugti Hills region have yielded the richest Tertiary vertebrate faunas to be found in Asia thus far. New fossils from five successive and distinct ‘bone beds’ bridge the supposed Oligocene sedimentary hiatus within the Sulaiman geological province; the lowermost continental levels of the previously described Miocene Chitarwata Formation, known as the Bugti Member, are Oligocene in age in the Bugti area. Neither a mixture of heterochronic faunal elements nor endemism of any fauna is evident in this area. Additional microfaunal material from the Bugti Member constrains an Oligocene age for the lower Chitarwata Formation in Zinda Pir (northeast of the Bugti Hills). This Oligocene transition between the marine Kirthar (Eocene) and continental Siwalik (Miocene) deposits consists of a regressive fluvio-deltaic system occupying a vast floodplain. It represents an early-stage molasse in the palaeo-Indus Basin which drained western orogenic highlands resulting from the collision between the Indian and Eurasian plates.
In the absence of a comprehensive pre‐Oligocene fossil record, the origin and early evolution of hystricognathous rodents have long been the subject of much uncertainty. Baluchimyinae (Rodentia) were initially interpreted as a subfamily of the ctenodactyloid Chappatimyidae (sciurognathous), a group considered to be endemic to the Indian subcontinent and to be closely related to hystricognathous rodents. A newly discovered early Oligocene hystricognathous rodent, Bugtimys zafarullahi gen. n. et sp. n., described herein, from the Bugti Hills (Balochistan, Pakistan) sheds new light on the higher level taxonomy of the previously described Baluchimyinae. As a contribution to the phylogenetic debates regarding the origin of Hystricognathi, we present a cladistic assessment of the dental evidence for the Palaeogene hystricognathous rodent cladogenesis. Our phylogenetic results consistently support the monophyly of the Hystricognathiformes clade (including Tsaganomyidae plus Hystricognathi) of which baluchimyine rodents are clearly members. There is, however, no support for the monophyly of a baluchimyine clade. Nonetheless, ‘baluchimyines’ are for the moment reinterpreted as Hystricognathi incertae sedis. Hystricognathous rodents appear to be well diversified at least since the early Oligocene, both in Africa and South America (phiomorphs and caviomorphs, respectively), and also now in south Asia. Furthermore, our phylogenetic results support close relationships between early hystricognathous and Asian ‘ctenodactyloid’ rodents, which clearly points to an Asian origin for Hystricognathi. In this phylogenetic framework, ‘baluchimyines’ and tsaganomyids are representatives of an initial phase of diversification of hystricognathous rodents in Asia. Oligocene phiomorphs and caviomorphs (sister groups) seem therefore to share a common ‘Asian’ hystricognathous ancestor. This reinforces the possibility that the early dispersal of hystricognathous rodents to South America was not from Africa but from Asia.
In the absence of a comprehensive fossil record, the origin and early evolution of Malagasy lemurs have been subject to much uncertainty. We report here the discovery of a strepsirrhine fossil with strong cheirogaleid lemur affinities, Bugtilemur mathesoni gen. et sp. nov., from early Oligocene deposits of the Bugti Hills (Balochistan, Pakistan). Bugtilemur represents the earliest record of Lemuriformes, which hence appear to have already diversified outside of Madagascar at least 30 million years ago. This fossil clearly enhances the critical role of the Indian subcontinent in the early diversification of lemurs and constrains paleobiogeographic models of strepsirrhine lemur evolution.
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