An additional specimen of a large-bodied Miocene hominoid from Chiang Muan, northern Thailand

Chiang Muan is the first Miocene fossil site in Southeast Asia, from which large-bodied Miocene hominoids have been discovered (Kunimatsu et al., Primate Res 16:299, 2000a). In this article, we describe a hominoid lower molar (CMu15-501) recovered from the Upper Lignite Member of Chiang Muan. The age of Chiang Muan is estimated to be latest Middle or earliest Late Miocene (around 11 Ma), based on the mammalian fauna.This revised version was published online in April 2005 with corrections to the cover date of the issue.     

L’industrie lithique du site Pléistocène inférieur de Pirro Nord (Apricena, Italie du sud) : une occupation humaine entre 1,3 et 1,7 Ma

The site of Pirro Nord (also known as Cava Pirro or Cava Dell’Erba) is known in literature since the 1970's of the last century as a palaeontological site, of which the mammalian fossil association constitutes a reference (local) fauna for the European latest Villafranchian. This fossil association is also known for the occurrence of some African elements. During the 2005, a lithic industry has been found in three karst fissures, together with the typical elements of the Pirro Nord vertebrate assemblage. The biochronological assessment based on the vertebrate assemblage attributes it to a time interval bracketed between 1.3 Ma and 1.7 Ma. Thus the site of Pirro Nord represents the oldest human occupation of Europe so far known. The lithic assemblage, attributable to the Mode 1, is constituted by three cores and seven flakes, and is made only on flint. Lithic artefacts have been found in stratigraphic context during the preliminary surveys of the three fissures, that they will be the object of systematic excavations in the years to come.     

Les Megacricetodon du gisement karstique miocène moyen de Blanquatère 1 (Pyrénées-Orientales, Sud de la France) : nouvelles espèces, implications biochronologique et phylogénique

Three Megacricetodon species are recognized in the Middle Miocene locality of Blanquatère 1 (Languedoc-Roussillon province, France). Two are new, the small-sized M. tautavelensis nov. sp. the medium to large-sized M. aunayi nov. sp., the third one being the already known M. “collongensis-gersii”, a medium-sized species found in other Miocene localities of the area. Size and morphology differentiate these species. Such a high number of contemporaneous species of the genus Megacricetodon is found for the first time in a Miocene locality in the region and indicate that the evolution of this genus in western Europe is likely more complicated. It may testify both of a biogeographical differentiation and of migration events. According to our calibration charts, the deposit is dated ca. 16 Ma ago. The position of Vieux-Collonges (MN 5) and Sansan (MN 6) on the biochronological scale is also discussed, as well as the estimated age of the biozonal boundaries MN 3/MN 4, MN 4/MN 5 and MN 5/MN 6.     

Small mammal (rodents and lagomorphs) European biogeography from the Late Oligocene to the mid Pliocene

Aim To analyse the fossil species assemblages of rodents and lagomorphs from the European Neogene in order to assess what factors control small mammal biogeography at a deep‐time evolutionary time‐scale. Location Western Europe: 626 fossil‐bearing localities located within 31 regions and distributed among 18 successive biochronological units ranging from c. 27 Ma (million years ago; Late Oligocene) to c. 3 Ma (mid Pliocene). Methods Taxonomically homogenized pooled regional assemblages are compared using the Raup and Crick index of faunal similarity; then, the inferred similarity matrices are visualized as neighbour‐joining trees and by projecting the statistically significant interregional similarities and dissimilarities onto palaeogeographical maps. The inferred biogeographical patterns are analysed and discussed in the light of known palaeogeographical and palaeoclimatic events. Results Successive time intervals with distinct biogeographical contexts are identified. Prior to c. 18 Ma (Late Oligocene and Early Miocene), a relative faunal homogeneity (high interregional connectivity) is observed all over Europe, a time when major geographical barriers and a weak climatic gradient are known. Then, from the beginning of the Middle Miocene onwards, the biogeography is marked by a significant decrease in interregional faunal affinities which matches a drastic global climatic degradation and leads, in the Late Miocene (c. 11 Ma), to a marked latitudinal pattern of small mammal distribution. In spite of a short rehomogenization around the Miocene/Pliocene boundary (6–4 Ma), the biogeography of small mammals in the mid Pliocene (c. 3 Ma) finally closely reflects the extant situation. Main conclusions The resulting biogeographical evolutionary scheme indicates that the extant endemic situation has deep historical roots corresponding to global tectonic and climatic events acting as primary drivers of long‐term changes. The correlation of biogeographical events with climatic changes emphasizes the prevalent role of the climate over geography in generating heterogeneous biogeographical patterns at the continental scale.     

Mountain uplift explains differences in Palaeogene patterns of mammalian evolution and extinction between North America and Europe

Patterns of late Palaeogene mammalian evolution appear to be very different between Eurasia and North America. Around the Eocene–Oligocene (EO) transition global temperatures in the Northern Hemisphere plummet: following this, European mammal faunas undergo a profound extinction event (the Grande Coupure), while in North America they appear to pass through this temperature event unscathed. Here, we investigate the role of surface uplift to environmental change and mammalian evolution through the Palaeogene (66–23 Ma). Palaeogene regional surface uplift in North America caused large-scale reorganization of precipitation patterns, particularly in the continental interior, in accord with our combined stable isotope and ecometric data. Changes in mammalian faunas reflect that these were dry and high-elevation palaeoenvironments. The scenario of Middle to Late Eocene (50–37 Ma) surface uplift, together with decreasing precipitation in higher-altitude regions of western North America, explains the enigma of the apparent lack of the large-scale mammal faunal change around the EO transition that characterized western Europe. We suggest that North American mammalian faunas were already pre-adapted to cooler and drier conditions preceding the EO boundary, resulting from the effects of a protracted history of surface uplift.     

Diversification and extinction patterns among Neogene perimediterranean mammals

The best mammalian fossil record during the Neogene of Western Europe is that of the rodents, the most successful and diversified mammal order. The study of origination and extinction during the Neogene (24-3 Ma BP) in one of the best-documented areas, Spain and southern France, gives an insight into the dynamics of these communities and indicates the possible nature of the driving forces. Three main periods of time show a high rate of origination: the late Burdigalian (17.5 Ma BP), the early Vallesian (11.5-11 Ma BP) and the early Pliocene (4.2-3.8 Ma BP). Two of these high origination-rate periods are immediately followed by important extinction events during which all cohorts are deeply affected (11.5-11 Ma BP and 4.2-3.8 Ma BP). The most important extinction event seems to occur during the early Vallesian (11.5-11 Ma BP), which probably includes the middle/late Miocene boundary. At the Miocene/Pliocene boundary, and during the early Pliocene, the faunal turnover seems to become faster, inducing a strong decrease of the mean species duration. Whereas the main immigration event, which occurs at 17.5 Ma BP, can be related to other faunal migrations in terms of the closure of the Tethys, as it occurs also in eastern Africa and in southwest Asia, the middle/late Miocene boundary event may have been related to a period of ice growth in the Southern Hemisphere. The extinction event that affects the planktonic foraminifera at 12 Ma BP cannot be chronologically correlated to this southwestern European land-mammal extinction event, because the calibration of the marine fossil record during that time-span has to be precise. Some limited terrestrial faunal exchanges that occur during the Messinian between southwestern Europe and northwestern Africa do not deeply affect the general faunal dynamics. Both allochthonous cohorts of immigrants become rapidly extinct. Several endemic rodent faunas, indicating insular conditions, have been reported from the southern edge of the western European continent from the middle Miocene up to the Pliocene. All show low taxonomic diversity, strong endemism and short survival. Some of them, like those of the Gargano Islands during the late Miocene, underwent peculiar morphological changes and also speciation. The large number of rodent genera coevolving in the Gargano Islands is indicative of the large surface areas of these islands. The general geographic pattern of southwestern Europe during the Neogene may therefore correspond to a large continental province including Spain and southern France with some kind of fast-modifying archipelago on its southern rim.     

Miocene to Pliocene vegetation reconstruction and climate estimates in the Iberian Peninsula from pollen data

Pollen analysis of Miocene and Pliocene sediments from the Iberian Peninsula shows a progressive reduction in plant diversity through time caused by the disappearance of thermophilous and high-water requirement plants. In addition, an increase in warm-temperate (mesothermic), seasonal-adapted “Mediterranean” taxa, high-elevation conifers and herbs (mainly Artemisia) occurred during the Middle and Late Miocene and Pliocene. This has mainly been interpreted as a response of the vegetation to global and regional processes, including climate cooling related to the development of the East Antarctic Ice Sheet and then the onset of the Arctic Ice Sheet, uplift of regional mountains related to the Alpine uplift and the progressive movement of Eurasia towards northern latitudes as a result of the northwards subduction of Africa. The development of steppe-like vegetation in southern Iberia is ancient and probably started during the Oligocene. The onset of a contrasted seasonality in temperature during the Mid-Pliocene superimposed on the pre-existing seasonality in precipitation, the annual length of which increased southward. The Mediterranean climatic rhythm (summer drought) began about 3.4 Ma and caused the individualization of modern Mediterranean ecosystems. Quaternary-type Mediterranean climatic fluctuations started at 2.6 Ma (Gelasian) resulting in repeated steppe vs. forest alternations. A latitudinal climatic gradient between the southern and the northern parts of the Iberian Peninsula existed since the Middle Miocene.     

Geochronological and Taxonomic Revisions of the Middle Eocene Whistler Squat Quarry (Devil’s Graveyard Formation,Texas) and Implications for the Early Uintan in Trans-Pecos Texas

The Whistler Squat Quarry (TMM 41372) of the lower Devil’s Graveyard Formation in Trans-Pecos Texas is a middle Eocene fossil locality attributed to Uintan biochronological zone Ui1b. Specimens from the Whistler Squat Quarry were collected immediately above a volcanic tuff with prior K/Ar ages ranging from ∼47–50 Ma and below a tuff previously dated to ∼44 Ma. New ⁴⁰Ar/³⁹Ar analyses of both of the original tuff samples provide statistically indistinguishable ages of 44.88±0.04 Ma for the lower tuff and 45.04±0.10 Ma for the upper tuff. These dates are compatible with magnetically reversed sediments at the site attributable to C20r (43.505–45.942 Ma) and a stratigraphic position above a basalt dated to 46.80 Ma. Our reanalysis of mammalian specimens from the Whistler Squat Quarry and a stratigraphically equivalent locality significantly revises their faunal lists, confirms the early Uintan designation for the sites, and highlights several biogeographic and biochronological differences when compared to stratotypes in the Bridger and Uinta Formations. Previous suggestions of regional endemism in the early Uintan are supported by the recognition of six endemic taxa (26% of mammalian taxa) from the Whistler Squat Quarry alone, including three new taxa. The revised faunal list for the Whistler Squat Quarry also extends the biostratigraphic ranges of nine non-endemic mammalian taxa to Ui1b.     

Palynological evidence for Late Miocene-Pliocene vegetation evolution recorded in the red clay sequence of the central Chinese Loess Plateau and implication for palaeoenvironmental change

In northern China, the Late Miocene-Pliocene red clay in the eastern Loess Plateau fills a gap of climate records between the well-known loess-soil sequences of the last 2.6 Ma and the Miocene loess-soil sequences from the western Loess Plateau. Previous studies indicate that the red clay is also of wind-blown origin, covering the period from ∼ 7-8 to ∼ 2.6 Ma. The red clay therefore provides a good archive to reconstruct paleoecological succession and paleoclimate change. In this study, a palynological investigation was conducted on the late Miocene-Pliocene red clay sequence at Xifeng, central Loess Plateau, which provides new insights into the nature of the evolution of vegetation and climate change from ∼ 6.2 to ∼ 2.4 Ma. Our results show that during this period the central Loess Plateau region was covered mainly by a steppe vegetation, indicating long lasting dry climatic condition. Three vegetational zones were recognized during this period. Zone A (∼ 6.2 to ∼ 5.8 Ma) is characterized by a steppe ecosystem; Zone B (∼ 5.8 to ∼ 4.2 Ma) is characterized by a significant increase of temperate forest plants, indicating a relatively humid regional climate; Zone C (∼ 4.2 to ∼ 2.4 Ma) indicates a typical steppe ecosystem. The vegetation shift at about 4.5-3.7 Ma, when the temperate forest plants decrease, the vegetation gradually changed to typical grassland and even to desert steppe. This is interpreted to represent a drying event. The uplift of the Tibetan Plateau at about 4.5 Ma that resulted in the intensification of the monsoon reversal is thought to have played an important role in this significant ecological change. High-latitude cooling may have partially contributed to the climate shift during ∼ 4.5 to ∼ 3.7 Ma in the Loess Plateau region, and most likely was the driving force for the ecological shift at about 3.7 Ma.     

The Middle Miocene climatic transition in the Southern Ocean: Evidence of paleoclimatic and hydrographic changes at Kerguelen plateau from planktonic foraminifers and stable isotopes

Middle Miocene (14.8–11.9 Ma) deep-sea sediments from ODP Hole 747A (Kerguelen Plateau, southern Indian Ocean) contain abundant, well-preserved and diverse planktonic foraminiferal assemblages. A detailed study of the climatic and hydrographic changes that occurred in this region during the Middle Miocene Climatic Transition led to the identification of an intense cooling phase (the Middle Miocene Shift). Abundance fluctuations of planktonic foraminiferal species with different paleoclimatic affinities, and oxygen and carbon stable isotopes have been integrated in a multi-proxy approach. Reconstruction of changes in foraminiferal faunal composition and diversity through time were the basis for identification of three foraminiferal biofacies. The most prominent faunal change took place at 13.8 Ma, when a fauna with warm-water affinity (marked by high abundance of Globorotalia miozea group and Globoturborotalita woodi plexus) was replaced by an oligotypic, opportunistic fauna with typical polar characters and dominated by neogloboquadrinids. This faunal change is interpreted as the result of foraminiferal migration from adjacent bioprovinces, caused by modifications in climate and hydrography. A positive 2.0‰ shift in δ¹⁸O (interpreted as the Mi3 event) and a related positive 1.0‰ shift in δ¹³C (corresponding to the CM6 event) accompanied this faunal turnover. These are interpreted to reflect substantial reorganization of Southern Ocean waters, the northward migration of the Polar Front and a strong increase in primary productivity. The second faunal change took place at 12.9 Ma and was characterized by the gradual decrease in abundance of the neogloboquadrinids and the recovery of Globorotalia praescitula/scitula group and Globigerinita glutinata. A positive 1.5‰ shift in δ¹⁸O (interpreted as the Mi4 event) and a concurrent gradual negative shift in δ¹³C accompanied this faunal change, witnessing further modifications of the climate/ocean system. Variations in sea surface temperature, considered as the main factor causing changes of surface hydrography at the Kerguelen Plateau, seem to have been driven by obliquity and long-term eccentricity, thus suggesting a key role played by the astronomical forcing on the evolution of Southern Ocean dynamics during the Middle Miocene. Also an evident 1.2 Myr modulation of the δ¹³C record suggests a main control of the long-term obliquity cycles on the carbon cycle dynamics. Particularly, the Mi3/CM6 events exactly fit with a node of the 1.2 Myr modulation cycles. This confirms the key role played by orbital parameters on high-latitude temperatures and Antarctic ice volume, and indirectly on global carbon burial and/or productivity. This climatic transition was marked also by changes in surface hydrography. From 14.8 to 13.8 Ma an intermediate-strength thermocline controlled by seasonality developed just below the photic zone. Weaker seasonality characterized the interval from 13.8 to 12.9 Ma, when the thermocline became shallower and sharper and favored intermediate-water foraminifers. From 12.9 Ma, seasonality increased again and an intermediate-strength thermocline re-developed.     

Gliridae (Rodentia,Mammalia) with a simple dental pattern: a new genus and new species from the European Early and Middle Miocene

A new genus of Gliridae, Simplomys gen. nov. is proposed. It contains glirids with a simplified dental pattern from the European Early and Middle Miocene. Simplomys gen. nov. includes several species originally described as Pseudodryomys such as Simplomys simplicidens, Simplomys robustus, Simplomys julii, and Simplomys aljaphi. In addition, a new species, Simplomys meulenorum sp. nov. , is proposed from the Spanish Miocene. The species of this genus share not only a very reduced and simplified dental morphology, but also unique dental proportions that clearly separate them from any other genera of Gliridae. Simplomys gen. nov. is recorded in most of the fossil faunas from the Early and Middle Miocene of the Iberian Peninsula, and shows the maximum diversity in this area during Mammal Neogene Zones MN 3 and MN 4. The genus has been also recorded in other European countries such as France, Germany, and Switzerland, conferring to this very characteristic taxon an important role for biochronological correlations within the European continent. © 2009 The Linnean Society of London, Zoological Journal of the Linnean Society, 2009, 157 , 622–652.     

Some considerations on small mammal evolution in Southern Germany,with emphasis on Late Burdigalian–Earliest Tortonian (Miocene) cricetid rodents

The recent advances regarding the complex chronobiostratigraphy of Middle Miocene terrestrial deposits of southern Germany are reviewed. We propose new and revised correlations between the Swiss and South German faunas framework for ongoing research. We restrict our analysis to the cricetid and microtoid muroid rodents, especially the Megacricetodon and cricetodontine groups, because of their importance for this purpose. Faunal turnovers reflect global climate changes. Species level endemism is punctuated by several immigration events, and a possible westward spread of faunal associations is suggested at around 13.8 Ma and, at the end of the Middle Miocene, by introduction of Late Miocene lineages from the east.     

Stratigraphic interpretation of the Kulu Formation (Early Miocene, Rusinga Island, Kenya) and its implications for primate evolution

Early Miocene fossils from Rusinga Island, Kenya, provide some of the best evidence for catarrhine evolution and diversification, and, together with more than eighty-five other mammalian species, form an important comparative reference for understanding faunal succession in East Africa. While there is consensus over the stratigraphic position of most of Rusinga's volcaniclastic deposits, the lacustrine Kulu Formation has been placed in various parts of the geological sequence by different researchers. To resolve this discrepancy, we conducted detailed geological analyses which indicate that the Kulu Formation was formed in the Early Miocene during a period of volcanic inactivity and subsidence following the early, mainly explosive hyper-alkaline phase of the Kisingiri complex and prior to the final eruptions of nephelinitic lavas. The underlying Hiwegi and older formations were locally deformed and deeply eroded before sedimentation began in the Kulu basin, so that the Kulu sediments may be significantly younger than the 17.8 Ma Hiwegi Formation and not much older than the overlying Kiangata Agglomerata-Lunene Lava series, loosely dated to ca. 15 Ma. The overall similarities between Kulu and Hiwegi faunas imply long-term ecological stability in this region. Our stratigraphic interpretation suggests that the Kulu fauna is contemporaneous with faunas from West Turkana, implying that differences between these assemblages—particularly in the primate communities—reflect paleobiogeographic and/or paleocological differences. Finally, the position of the Kulu Formation restricts the time frame during which the substantial faunal turnover seen in the differences between the primate and mammalian communities of Rusinga and Maboko Islands could have occurred.     

Bio-magnetostratigraphy and environment of the oldest Eurasian hominoid from the Early Miocene of Engelswies (Germany)

The paleobiogeography of hominoids exhibits a puzzling pattern of migrations between and within Africa and Eurasia. A precise dating of hominoid-bearing localities is therefore essential to reveal the timing, direction and possible causes of dispersals. Here, we present a bio-magnetostratigraphic analysis of the section of Engelswies (Southern Germany, Upper Freshwater Molasse, North Alpine Foreland Basin) where the oldest Eurasian hominoid was found. Our paleomagnetic results reveal a very short normal and a reverse magnetic polarity for the entire section. The polarity record is correlated to the Astronomical Tuned Neogene Time Scale using an integrated stratigraphic approach. This approach follows the chronostratigraphic framework for the Upper Freshwater Molasse, which combines magnetostratigraphy with biostratigraphic, lithostratigraphic and ⁴⁰Ar/³⁹Ar dating results. According to this outcome, the reverse polarity of the Engelswies section most likely correlates to magnetochron C5Cr. The origin of the short normal polarity remains enigmatic. The magnetostratigraphic calibration and the evolutionary level of the Engelswies small mammal fauna suggest an age of 17.1-17.0 Ma (Early Karpatian, Early Miocene) for the oldest Eurasian hominoid, and roughly confirm the estimates of Heizmann and Begun (2001). The estimated age suggests that the first hominoids in Eurasia are contemporaneous with Afro-Arabian afropithecins, and dispersal may have been facilitated by intra-Burdigalian (∼18-17 Ma) sea-level low stands and the beginning of the Miocene Climate Optimum. The paleoclimatic and environmental reconstruction of the Engelswies locality indicates a lakeshore environment near dense subtropical rain forest vegetation, where paratropical temperatures (mean annual temperature around 20 °C) and humid conditions (mean annual precipitation > 1.100 mm) prevailed.     

Contexte géographique et géologique du site de Kocabaş, Bassin de Denizli,Anatolie, Turquie

The site of Kocaba? is located in the Denizli Basin, in western Anatolia, 400 km southwest of Ankara, 360 km south of Istanbul, 200 km east-southeast of Izmir and 150 km northwest of Antalya. The Denizli Basin depression, at the junction of the Buyuk Menderes and Gediz grabens, which began to form at the beginning of the Miocene, was filled in around the edges, along fault lines, by significant travertine formations, some of which are still active today. The age of the Kocaba? travertines, which yielded the Kocaba? Homo erectus skullcap, was evaluated by thermoluminescence at 828,000 years, by electron spin resonance (ESR) at 1,110,000 years and by the ²⁶Al/¹⁰Be cosmogenic nuclide method to more than 1.22 Ma and less than 1.5 Ma, a date which has been confirmed by magnetostratigraphy and biochronology.     

Khoratpithecus piriyai, a Late Miocene hominoid of Thailand

A Khoratpithecus piriyai lower jaw corresponds to a well-preserved Late Miocene hominoid fossil from northeastern Thailand. Its morphology and internal structure, using a microcomputed tomography scan, are described and compared to those of other known Miocene hominoids. It originated from fluviatile sand and gravel deposits of a large river, and was associated with many fossil tree trunks, wood fragments, and large vertebrate remains. A biochronological analysis by using associated mammal fauna gives an estimated geological age between 9-6 Ma. The flora indicates the occurrence of a riverine tropical forest and wide areas of grassland. K. piriyai displays many original characters, such as the great breadth of its anterior dentition, suggesting large incisors, large lower M3, a canine with a flat lingual wall, and symphysis structure. Several of its morphological derived characters are shared with the orangutan, indicating sister-group relationship with that extant ape. This relationship is additionally strongly supported by the absence of anterior digastric muscle scars. These shared derived characters are not present in Sivapithecus, Ankarapithecus, and Lufengpithecus, which are therefore considered more distant relatives to the orangutan than Khoratpithecus. The Middle Miocene K. chiangmuanensis is older, displays more primitive dental characters, and shares several dental characters with the Late Miocene form. It is therefore interpreted as its probable ancestor. But its less enlarged M3 and more wrinkled enamel may suggest an even closer phylogenetic position to orangutan ancestors, which cannot yet be supported because of the incomplete fossil record. Thus Khoratpithecus represents a new lineage of Southeast Asian hominoids, closely related to extant great ape ancestors.     

Re-interpreting the biochronology of the La Celia and Los Gargantones mammal sites (Late Miocene,Murcia, Spain)

The biochronological age of the small-mammal populations of Los Gargantones 1, 2 and La Celia (upper Miocene, La Celia sub-basin, Murcia, Spain) is re-interpreted. The presence in Los Gargantones of Occitanomys adroveri, Parapodemus barbarae, Parapodemus cf. gaudryi, Huerzelerimys turoliensis, Atlantoxerus cf. adroveri, and Alilepus evidences a correlation to MN12 (∼7.5–7 Ma) rather than to MN11 (∼9–7.5 Ma), as inferred previously. The assemblage corresponds to that of the more eastern, near-coast sites of Crevillente 8 and 15, situated in the Alicante area. The stratigraphically highest site of La Celia contains Hispanomys adroveri, a species also indicative of MN12. The presence of Castromys cf. littoralis together with an advanced O. adroveri points to a slightly younger age than that of Los Gargantones, approaching that of MN13 sites. The assemblage best matches that of Crevillente 17. Other species described in this paper are Prolagus crusafonti, Prolagus sp., Parasorex cf. ibericus, Panelimnoecus cf. repenningi, and Blarinella aut Petenyia sp. indet.     

New Catarrhine fossils from Moroto II, Early Middle Miocene (ca 17.5 Ma) Uganda

During the 1998–2003 field seasons of the Uganda Palaeontology Expedition, dental remains of three catarrhine species were recovered from Moroto II, Uganda. Micromammals from the locality indicate a late Early Miocene to basal Middle Miocene (ca 17.5–17 Ma) age, younger than Rusinga (17.8 Ma), but similar in age to Buluk (17.2 Ma) and Kalodirr (17.2 Ma). This paper describes and interprets new catarrhines from the site, one of which is a victoriapithecid monkey, the second a new genus and species of small-bodied ape, and the third a large hominoid. A fourth species collected in the 1960's is attibuted to Afropithecus turkanensis. To cite this article: M. Pickford et al., C. R. Palevol 2 (2003).     

The spread of grass-dominated habitats in Turkey and surrounding areas during the Cenozoic: Phytolith evidence

The arrival of hipparionine horses in the eastern Mediterranean region around 11 Ma was traditionally thought to mark the simultaneous westward expansion of savanna vegetation across Eurasia. However, recent paleoecological reconstructions based on tooth wear, carbon isotopes, and functional morphology indicate that grasses played a minor role in Late Miocene ecosystems of the eastern Mediterranean, which were more likely dry woodlands or forests. The scarcity of grass macrofossils and pollen in Miocene floras of Europe and Asia Minor has been used to support this interpretation. Based on the combined evidence, it has therefore been suggested that Late Miocene ungulate faunal change in the eastern Mediterranean signals increased aridity and landscape openness, but not necessarily the development of grass-dominated habitats.

To shed new light on the Miocene evolution of eastern Mediterranean ecosystems, we used phytolith assemblages preserved in direct association with faunas as a proxy for paleovegetation structure (grassland vs. forest). We extracted phytoliths and other biogenic silica from sediment samples from well-known Early to Late Miocene ( 20–7 Ma) faunal localities in Greece, Turkey, and Iran. In addition, a Middle Eocene sample from Turkey yielded phytoliths and served as a baseline comparison for vegetation inference.

Phytolith analysis showed that the Middle Eocene assemblage consists of abundant grass phytoliths (grass silica short cells) interpreted as deriving from bambusoid grasses, as well as diverse forest indicator phytoliths from dicotyledonous angiosperms and palms, pointing to the presence of a woodland or forest with abundant bamboos. In contrast, the Miocene assemblages are dominated by diverse silica short cells typical of pooid open-habitat grasses. Forest indicator phytoliths are also present, but are rare in the Late Miocene (9–7 Ma) assemblages. Our analysis of the Miocene grass community composition is consistent with evidence from stable carbon isotopes from paleosols and ungulate tooth enamel, showing that C₄ grasses were rare in the Mediterranean throughout the Miocene. These data indicate that relatively open habitats had become common in Turkey and surrounding areas by at least the Early Miocene ( 20 Ma), > 7 million years before hipparionine horses reached Europe and arid conditions ensued, as judged by faunal data.     

India at the cross-roads of human evolution

The Indian palaeoanthropological record, although patchy at the moment, is improving rapidly with every new find. This broad review attempts to provide an account of (a) the Late Miocene fossil apes and their gradual disappearance due to ecological shift from forest dominated to grassland dominated ecosystem around 9-8 Ma ago, (b) the Pliocene immigration/evolution of possible hominids and associated fauna, (c) the Pleistocene record of fossil hominins, associated fauna and artifacts, and (d) the Holocene time of permanent settlements and the genetic data from various human cultural groups within India. Around 13 Ma ago (late Middle Miocene) Siwalik forests saw the emergence of an orangutan-like primate Sivapithecus. By 8 Ma, this genus disappeared from the Siwalik region as its habitat started shrinking due to increased aridity influenced by global cooling and monsoon intensification. A contemporary and a close relative of Sivapithecus, Gigantopithecus (Indopithecus), the largest ape that ever-lived, made its first appearance at around 9 Ma. Other smaller primates that were pene-contemporaneous with these apes were Pliopithecus (Dendropithecus), Indraloris, Sivaladapis and Palaeotupia. The Late Pliocene and Early Pleistocene witnessed northern hemisphere glaciations, followed by the spread of arid conditions on a global scale, setting the stage for hominids to explore “Savanahastan”. With the prominent expansion of grassland environments from East Africa to China and Indonesia in the Pliocene, monkeys and baboons dispersed into the Indian subcontinent from Africa along with other mammals. Though debated, there are several claims of the presence of early hominins in this part of the world during the Late Pliocene, based primarily on the recovery of Palaeolithic tools. Fossils of our own ancestor and one of the first globe-trotters, early Homo erectus, has been documented from the Early Pleistocene of East Africa, Western Asia and Southeast Asia, thus indirectly pointing towards Indian subcontinent as a possible migration corridor between these regions. The only definite pre-Homo sapiens fossil hominin remains come from the Central Narmada Valley and are thought to be of Middle to late Pleistocene age, and the cranium has been shown to be closely linked to archaic Homo sapiens/H. heidelbergensis of Europe. Around ∼74,000 yrs ago, a super volcanic eruption in Sumatra caused the deposition of Youngest Toba Tephra, that covered large parts of the Indian peninsula. Just around this time anatomically-and-behaviorally modern humans or Homo sapiens possibly arrived into India as evidenced by the so called Middle and Upper Palaeolithic assemblages and associated symbolic evidence. The available genetic data reveals that the gene pool to which modern Indians races belong was extremely diverse and had variable mixed links with both European and Asian populations.