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.     

A new Miocene fauna of snakes from eastern Siberia,Russia.: Was the snake fauna largely homogenous in Eurasia during the Miocene?

Togay, a locality from Ol’khon Island, Baykal Lake, Russia, has yielded a fauna of snakes of Late Middle or early Late Miocene age. It is located in a broad area from which no Neogene snake has been reported; therefore, it represents an important landmark. The fauna includes a non-erycine boid, two or three colubrids, a viperid of the ‘oriental complex’ of Vipera, and perhaps another viperid. This assemblage is astonishingly reminiscent of the snake faunas from the late Early and early Middle Miocene from western and central Europe, it being understood that Miocene faunas are practically unknown in the geographically intermediary area. It may be entertained whether a homogenous snake fauna inhabited Eurasia (except the southern part of the continent) during the Miocene.     

Creodonts and carnivores from the Middle Miocene Muruyur Formation at Kipsaraman and Cheparawa,Baringo District,Kenya

The Middle Miocene Muruyur Formation (ca 14.5 Ma), Tugen Hills, Kenya, has yielded a huge creodont and a variety of carnivores ranging in size from mongoose-sized viverrids and herpestids to lion-sized amphicyonids. The fauna partly fills what used to be a major gap in our knowledge of Neogene African carnivores, spanning the period between the better known Early Miocene assemblages of western Kenya and eastern Uganda, and the Late Miocene and Plio–Pleistocene faunas of East Africa. Present in the deposits are Megistotherium, two species of Hecubides, one species of Agnotherium, Herpestes, Vishnuictis, and one or two undetermined felids.     

The importance of Late Miocene faunal exchanges between Eastern Mediterranean areas and Central Europe

Recent studies of mammal faunas from the Vienna and Pannonian Basins—in particular the assemblage from Kohfidisch in Burgenland (Austria)—provide new data on the faunal turnover at the Vallesian—Turolian transition. They demonstrated a considerable influence of the faunal exchanges between Greco-Iranian, Eastern European and Central European faunal provinces on renewal of mammal communities in Central Europe, particularly at MN10/MN11 boundary around 8.7 Ma. Five new comers from the Balkano-Iranian region (Gazella aff. pigrimi, ?Nisidorcas, Tragoportax gaudryi, Protoryx and Palaeoryx) coexisted in the Early Turolian of Central Europe with the Middle Miocene autochthonous (Orygotherium, Dorcatherium naui, Micromeryx, Euprox, Amphiprox anocerus and Miotragocerus pannoniae) and Late Miocene invaders from Eastern Europe (Procapreolus and Cervavitus). Dispersal events were close related to palaeoenvironmental and climatic changes.     

The Permian fusulinoidean faunas of the Sibumasu and Baoshan blocks: their implications for the paleogeographic and paleoclimatologic reconstruction of the Cimmerian Continent

Permian fusulinoidean faunas occur in mainly four stratigraphic levels in the Baoshan Block of West Yunnan and the Sibumasu Block of Southeast Asia, which constituted part of the eastern Cimmerian Continent. The oldest fauna, from the upper part of the Dingjiazhai Formation in the Baoshan Block, consists of Pseudofusulina, Eoparafusulina, and a new boultoniid genus, and is assignable to the Yakhtashian (=Artinskian). The second one, which occurs in the basal part of the Ratburi Limestone and its equivalent strata in the Sibumasu Block, is represented by Monodiexodina, and is probably referable to the Bolorian (=Kungurian). The third fauna, composed of Eopolydiexodina, Rugososchwagerina, Yangchienia, Chusenella, Jinzhangia, and several other genera, is dated to the Murgabian (=Wordian), and occurs in the lower part of the Shazipo and Daaozi formations in the Baoshan Block and the main part of the Ratburi Limestone in the Sibumasu Block. The youngest fauna of probably Dzhulfian (=Wuchiapingian) age is found in the upper part of the Ratburi Limestone, and contains Nanlingella, Reichelina, Codonofusiella?, and a few staffellid genera. A smaller foraminiferal genus, Shanita, found from the upper part of the Ratburi Limestone and the upper part of the Shazipo Formation is also an important element of the foraminiferal assemblage near the Midian-Dzhulfian (=Capitanian-Wuchiapingian) boundary in the Baoshan and Sibumasu blocks.In the eastern Cimmerian Continent, low generic diversity throughout the Permian and the paucity of Tethys-characterizing neoschwagerinid and verbeekinid genera during Middle Permian time are two remarkable features of the Permian fusulinoidean faunas. In the Cimmerian Continent, the generic diversity of Permian fusulinoidean faunas in space and time gradually increases from the Early Permian to late Middle Permian as well as from the eastern Cimmerian areas to western ones. The temporal increase of the generic diversity can be explained by the northward drift of the Cimmerian Continent during Permian time. In contrast, the lower generic diversity of the eastern Cimmerian Permian fusulinoidean faunas against western ones is possibly due to an oblique arrangement of the continent to paleolatitude. Thus, the western Cimmerian Continent was more proximal to the tropical Tethyan domain than its eastern part. In addition, the Middle Permian Cimmerian paleobiogeographic region is likely to be subdivided into two subregions, the western Tethyan Cimmerian and the eastern Gondwanan Cimmerian, based on the distribution pattern of verbeekinid and neoschwagerinid fusulinoideans and overall generic diversity. The scarce occurrence or total absence of these essentially Tethys-indicating fusulinoideans in the Baoshan and Sibumasu blocks suggests that the eastern Cimmerian Continent was still far from the equatoro-tropical Cathaysian domain and was probably in a warm temperate or subtropical zone until the end of the Permian. The eastern Cimmerian areas finally migrated into a tropical zone by the Late Triassic judging from well-developed Carnian sponge-coral buildups in the Chaiburi Formation in the Sibumasu Block.     

Badenian and Sarmatian s.str. from the Carpathian area: Overview and ongoing research on Hungarian and Romanian small vertebrate evolution

The fossil record from the Carpathian area plays a key role for the understanding of the processes leading to the faunal interchanges between western Europe and Asia Minor during the late part of the Middle Miocene. Important mammal successions are now available from the Central Paratethys, especially Hungary and Romania. Here, we present the current state-of-the-art of the ongoing research concerning these faunas, especially small mammals and herpetofauna. We underscore the relevance of the Middle to earliest Late Miocene fossil record from these countries for chrono(bio)stratigraphic and palaeoenvironmental studies at the Eurasian scale.     

Italian Cenozoic crocodilians: taxa, timing and palaeobiogeographic implications

Crocodylian remains are collected in 39 fossil-bearing localities but only in seven localities specimens with reliable taxonomic attributions, at least to genus level have been collected. Three species have been reported from the early Lutetian Purga di Bolca site: Pristichampsus cf. Pristichampsus rollinati, Asiatosuchus sp., Hassiacosuchus sp. (=Allognathosuchus sp.). The three crocodilians discovered at Purga di Bolca have been reported also from Geiseltal and Messel (Middle Eocene, Germany). Bolca at that time was part of a Tethysian archipelago and no mammals have been found there till now. Crocodilians and turtles clearly arrived from the European mainland across a marine water barrier. Among the other fossiliferous localities of Veneto, very interesting is the Monte Zuello site, of late Middle Eocene age, yielding a longirostrine crocodilian, Megadontosuchus arduini, a tomistomine species. Tomistomines are known in contemporaneous sediments of both Europe and Africa, but the European forms Dollosuchus and Kentisuchus seem the closest taxa. Remains of Oligocene age have been collected in Veneto and Liguria, but the fossils discovered in the second region are teeth or fragmented bones. The fossil crocodilians of Monteviale (Veneto), of Early Oligocene age, have been assigned to two species but they have been recently all identified as Diplocynodon ratelii, known from several European sites of Late Eocene, Oligocene and Miocene age. This species arrived in the Monteviale area from the European mainland across a narrow sea. Several crocodilian fossils of Miocene age are very fragmentary or represented by isolated teeth. In the Middle and Late Miocene of Sardinia, a well-established species, Tomistoma calaritanum is present. Remains of Tomistoma of the same age have been reported in some localities in Tuscany, Apulia, Sicily and Malta. In the Mediterranean area, the genus is known from European and African sites (of older age). The colonisation of Europe by this genus is the result of a dispersion from Africa (or less probably from Asia). During Late Miocene Sardinia and Tuscany belong to the same palaeobioprovince characterized by the Oreopithecus-Maremmia fauna. In Tuscany, a crocodilian identified as Crocodylus bambolii is present in the late Miocene site of Monte Bamboli. If the generic attribution of this form is correct, its ancestors must have arrived from Africa. Another fossil assemblage of Late Miocene age characterizes the Apulia-Abruzzi palaeobioprovince (Hoplitomeryx-Microtia fauna) and testifies complete isolation between the two palaeobioprovinces. In this last area, remains of Crocodylus sp. have been collected in coastal sandstones at Scontrone (Abruzzi) and in several fissure fillings of Gargano of slightly younger age. The ancestors of this species arrived from Africa while no African elements are present among the mammalian fauna. The dispersion of the genus Crocodylus in the Italian palaeoislands may have taken place once, with allopatric differentiation of the two populations (Tuscany-Sardinia and Apulia-Abruzzi) or twice with independent colonisation of each area.     

Provinciality of the Mediterranean lower Jurassic brachiopod fauna: Causes and plate-tectonic implications

The composition of 23 “NW European” and “Mediterranean” Lower Jurassic (Pliensbachian) brachiopod faunas is compared at the species level. On the basis of this quantitative approach, the two “provinces” can be delimited more sharply than by earlier qualitative studies. In the author's opinion the most reasonable cause of the provinciality is as follows: in the Middle Triassic a segment of the European shelf became rifted, detached and drifted toward the open Tethys ocean. Being isolated, the brachiopods of this province could produce evolutionary lineages different from the European ones. If the presence of this contiguous and separate Triassic—Jurassic microcontinent characterized by Mediterranean brachiopod faunas is assumed, this factor should be borne in mind in the reconstructions concerning the closure of the Tethys (= Alpine orogeny).     

柴达木盆地晚中新世三趾马化石

Bohlin描述的柴达木动物群中的三趾马材料非常少 ,仅能证明三趾马在这个地点的存在。近年来新的野外考察在这一地区发现了更多的三趾马化石材料 ,至少包括 3个种 ,即Hipparioncf.H .chiai、H .weihoense和H .teilhardi。H .cf.H .chiai和H .weihoense在柴达木盆地的发现进一步证实了晚中新世早期 (保德早期 )动物群在这个地区的存在。柴达木盆地的H .teilhardi基本上与H .cf.H .chiai和H .weihoense产自同一层位 ,其时代也应为保德早期。H .cf.H .chiai和H .weihoense在柴达木盆地的发现为该地区在晚中新世早期为草原型环境的判断提供了更多的证据。H .teilhardi更细长的远端肢骨也是对开阔环境的一种适应性状     

Paleobiogeography of Mesozoic brachiopod faunas from Andean–Patagonian areas in a global context

During the Mesozoic, the Andean region has played a hinging role between high- and low-latitude faunas, which are, respectively, characterized by stocks that display long-term fidelity. This paper is aimed at providing an updated review of Late Triassic to Late Cretaceous South American articulated brachiopods in the light of previous knowledge at worldwide scale. Late Triassic brachiopods from the Argentine–Chilean Andes show unmistakable Maorian (or Notal) faunal elements alongside some more cosmopolitan genera, with certain influence of Eastern Pacific taxa. By Early Jurassic times, differentiation of Tethyan and Boreal Realms became progressively evident in Europe. In South America, Hettangian–Sinemurian brachiopod faunules from the Argentinian Andes are somewhat impoverished, with mostly cosmopolitan genera showing certain affinities to Maorian species, and with the addition of some endemics later. Increasingly, diverse Pliensbachian Andean brachiopods denote close relationships to Celto-Swabian taxa, then by Domerian times, a certain degree of endemism was developed, though somewhat delayed Tethyan influences, and persistent links with New Zealand are subordinately recognizable, too; most Toarcian assemblages reveal basically Celto-Swabian and Iberian affinities as well. East-west austral links across the Pacific may have been favored by migratory routes fringing the Gondwana margin, whereas faunal exchange with the western end of the Tethys appears to reflect an intermittent shallow-marine connection through the Hispanic Corridor. During the Middle Jurassic, distinction of Tethyan and Boreal Realms was maintained in the northern Hemisphere, and the differentiation of an Ethiopian or Southern Tethyan fauna became better characterized. Aalenian and Bajocian brachiopods of the Andes display generic affinities mainly with those from western Europe, with some minor endemic developments; brachiopods recorded from the Bathonian–Callovian of Argentina (and Chile) also occur along the northern Tethyan margin, yet with some genera extending into Indo-Ethiopian areas. During the Late Jurassic, Boreal faunas from high-latitudes became even more strongly differentiated from low-latitude, Tethyan ones. Oxfordian and Tithonian brachiopods from the Andes apparently belong to genera of cosmopolitan or northern Tethyan affiliation, yet there are few elements in common with other eastern Pacific areas, such as Mexico. Early Cretaceous brachiopods, in addition to Andean basins of Chile and western Argentina, are known also from Patagonia and Tierra del Fuego. They belong mostly to widely distributed, mainly Tethyan genera, with some quasi-cosmopolitan and circum-Pacific components (some shared with Antarctica become noticeable). Late Cretaceous brachiopods from northern Patagonia show significant affinities to Maastrichtian ones of northwest Europe and central Asia, which calls for further assessing the potential role that may have played the trans-Saharan passageway in such dispersal. Broad aspects of Mesozoic brachiopod paleobiogeography are fairly well understood, yet details of ranking and naming of certain units are still in need of more agreement.     

Geopalaeontological setting,chronology and palaeoenvironmental evolution of the Baccinello-Cinigiano Basin continental successions (Late Miocene,Italy)

The Latest Miocene succession of the Baccinello-Cinigiano Basin in southern Tuscany (Italy) recorded a faunal turnover documenting the extinction of an older, insular, endemic faunal complex characterised by the extinct ape Oreopithecus bambolii and the setting of a new, continental, European faunal complex including the colobine monkey Mesopithecus. A similar turnover pattern (Late Miocene ape/Latest Miocene Cercopithecidae) is generally observed in Late Miocene continental successions of Eurasia, from Spain to central Europe, Southwest Europe, the near East, and Southwest Asia. Abundant literature reports that the Late Miocene Eurasian hominoid primate distribution closely tracks the climatic/environmental changes occurring during the 12–9 Ma interval, until their extinction in western Europe. In the primate record, the dispersion of Cercopithecidae and the contraction of hominids is interpreted as an event depicting a pattern of “continentalisation” in the Old World. The sedimentary succession of the Baccinello-Cinigiano basin, one of the longest continuous vertebrate-bearing continental successions in the Neogene Italian record, contributes to the debate on this hypothesis. This paper provides an overview of the main characteristics of the sedimentary succession, the chronological constraints (biochronology, radiometric datings, magnetostratigraphy), and the palaeoenvironmental evolution as derived from palaeobiological approaches and from the study of stable carbon and oxygen isotope contents along the entire sedimentary succession. The 2 myr geological history of the Baccinello Cinigiano Basin, which documents the evolutionary history of Oreopithecus and associated faunas, does not have a direct relation with the event of the Messinian Salinity Crisis. The evolutionary history of Baccinello-Cinigiano Basin and its palaeontological record have been mainly driven by the regional tectonism and palaeogeographic changes that affected the northern Tyrrhenian regions in Late Miocene (Latest Tortonian–Messinian) times.     

Late devonian facies inter-relationships in bordering areas of the North Atlantic and their palaeogeographic implications

Late Devonian faunal and facies relationships are examined in seven around the North Atlantic — in eastern North America, Greenland, western Europe and northwest Africa. A shallow marine (“littoral”) environment, characterized by the genus Cyrtospirifer, is distinguished from a deeper water (“bathyal”) goniatite-conodont milieu on the one hand, and from the “Old Red Sandstone” terrestial facies bearing plant an d fresh-water fish remains on the other.Current or source directions indicate that an “Acadian Divide” existed, separating west-flowing drainage systems in North America from those flowing to the east on the Afro-European side. All species of the osteolepid Latvius, and the majority of species of Glyptopomus are found on the eastern flank. Conversely, the earliest amphibian, Ichthyostega, may have been confined to the western side of the divide.Palaeogeographic reconstruction places northwest Africa fairly close to the Catskill Delta in the Late Devonian, thus accounting for the presence of an “American fauna” in the former. North—south migration of littoral faunas along the Afro-European shores was, however, apparently inhibited.     

Remains of sea turtles from the Ikovo locality (Lugansk Region, Ukraine; Middle Eocene)

Fragmentary remains of sea turtles (Cheloniidae sensu lato: Argillochelys sp., Puppigerus nessovi Averianov, 2005, and Cheloniidae gen. indet.) from the Ikovo locality (Lugansk Region, Ukraine; Lower Lutetian, Middle Eocene) are described. The genera Argillochelys and Puppigerus are recorded for the first time in Eastern Europe. The turtle assemblage from Ikovo is similar at the generic level to West European assemblages (Belgium, Great Britain) of approximately the same age (Lower-Middle Eocene). In the presence of P. nessovi, the Ikovo assemblage is similar to that from the Middle Eocene Dzheroi 2 locality (Uzbekistan).     

Palaeobotanical studies from tropical Africa: relevance to the evolution of forest, woodland and savannah biomes

Fossil plants provide data on climate, community composition and structure, all of which are relevant to the definition and recognition of biomes. Macrofossils reflect local vegetation, whereas pollen assemblages sample a larger area. The earliest solid evidence for angiosperm tropical rainforest in Africa is based primarily on Late Eocene to Late Oligocene (ca. 39-26 Myr ago) pollen assemblages from Cameroon, which are rich in forest families. Plant macrofossil assemblages from elsewhere in interior Africa for this time interval are rare, but new work at Chilga in the northwestern Ethiopian Highlands documents forest communities at 28 Myr ago. Initial results indicate botanical affinities with lowland West African forest. The earliest known woodland community in tropical Africa is dated at 46 Myr ago in northern Tanzania, as documented by leaves and fruits from lake deposits. The community around the lake was dominated by caesalpinioid legumes, but included Acacia, for which this, to my knowledge, is the earliest record. This community is structurally similar to modern miombo, although it is different at the generic level. The grass-dominated savannah biome began to expand in the Middle Miocene (16 Myr ago), and became widespread in the Late Miocene (ca. 8 Myr ago), as documented by pollen and carbon isotopes from both West and East Africa.     

柴达木盆地新近纪犀科化石新材料

近年来在青海柴达木盆地中新世地层内新发现的犀科化石 ,经研究有 3属 3种 ,即Ac erorhinustsaidamensis,Hispanotheriummatritense和Dicerorhinusringstromi,其中后两个种是在这一地区的初次报道。新材料虽较破碎 ,但其发现扩大了H .matritense和D .ringstromi的地理分布范围。更重要的是 ,柴达木动物群原来被确定为晚中新世早期 ,其主要依据是安琪马动物群的残余分子与三趾马动物群共生 ,而此次的发现证明这一地区确实有含H .matritense的中中新世动物群存在。D .ringstromi的发现还证明柴达木盆地有相当于保德动物群时代的晚中新世晚期沉积。     

Leaves and pollen of bamboos from the Polish Neogene

Recently discovered fossil bamboo leaves and pollen are described from the Neogene of Poland. Morphological analysis of fossil leaves from the Late Miocene deposits of the Bełchatów Lignite Mine, Central Poland have allowed them to be determined as “Bambusa” lugdunensis Saporta. It is the first record of this species in the Cenozoic of Poland. The fossils have been compared with other records of bamboos from the Cenozoic of Europe. Pollen grains from the Middle Miocene (Badenian) deposits from the Legnica brown coal deposit (Lower Silesia) provide additional evidence of bamboos. These are assigned to Graminidites bambusoides Stuchlik, and are similar to those of recent Arundinaria. We infer that plant (plants?) that produced the pollen of G. bambusoides could have grown in swamp forests and/or reed marshes. This report provides a general survey of the occurrence of bamboos in the European Neogene, from which the leaves and pollen documented here present important data on the distribution of this group of monocots in Poland and eastern Europe.     

Brittle stars from the upper Cenomanian of the Preafrican platform: First ophiuroid remains for the Cretaceous of Algeria

While Late Cretaceous ophiuroids are relatively well known in Europe, these faunas have been much less studied in North Africa. With the exception of some Tunisian assemblages preliminary described at the turn of the 21st century, nothing is known about the Cretaceous brittle stars of the southwestern Tethyan margin. The present paper seeks to bring the first data about hitherto unknown ophiuroids recently found in the early upper Cenomanian succession of the eastern side of the Preafrican trough (Menaguir section, Algeria). This “community” of brittle stars comprises at least eight species. Most of them are probably new, but have not been formally named here. These are representatives of the families Hemieuryalidae, Amphiuridae, Ophiodermatidae, Ophiacanthidae, Ophiopezidae and probably also Ophiomyxidae and Ophiobyrsidae. Almost all vertebrae are zygospondylous; no streptospondylous vertebrae indicate the absence of the order Euryalida here. Most of the ophiuroids belong to the orders Amphilepidida and Ophiacanthida. Ophiotitanos serrata, Ophiomyxa? aff. jekerica, Ophiojagtus? sp. and some other taxa resembling ophiuroid assemblages from the Late Cretaceous of central, western and northern Europe. With respect to the late Cenomanian age, the depth of the sea and the taxonomic composition, there are some similarities with ophiuroids of the Bohemian Cretaceous Basin. The mid-ramp subtidal facies suggests that brittle stars lived here in a warm, euphotic and probably shallow sea.     

Middle Eocene–Early Pliocene Subantarctic planktic foraminiferal biostratigraphy of Site 1090, Agulhas Ridge

The analysis of planktic foraminiferal assemblages from Site 1090 (ODP Leg 177), located in the central part of the Subantarctic Zone south of South Africa, provided a geochronology of a 330-m-thick sequence spanning the Middle Eocene to Early Pliocene. A sequence of discrete bioevents enables the calibration of the Antarctic Paleogene (AP) Zonation with lower latitude biozonal schemes for the Middle–Late Eocene interval. In spite of the poor recovery of planktic foraminiferal assemblages, a correlation with the lower latitude standard planktic foraminiferal zonations has been attempted for the whole surveyed interval. Identified bioevents have been tentatively calibrated to the geomagnetic polarity time scale following the biochronology of Berggren et al. (1995). Besides planktic foraminiferal bioevents, the disappearance of the benthic foraminifera Nuttallides truempyi has been used to approximate the Middle/Late Eocene boundary. A hiatus of at least 11.7 Myr occurs between 78 and 71 m composite depth extending from the Early Miocene to the latest Miocene–Early Pliocene. Middle Eocene assemblages exhibit a temperate affinity, while the loss of several planktic foraminiferal species by late Middle to early Late Eocene time reflects cooling. During the Late Eocene–Oligocene intense dissolution caused impoverishment of planktic foraminiferal assemblages possibly following the emplacement of cold, corrosive bottom waters. Two warming peaks are, however, observed: the late Middle Eocene is marked by the invasion of the warmer water Acarinina spinuloinflata and Hantkenina alabamensis at 40.5 Ma, while the middle Late Eocene experienced the immigration of some globigerinathekids including Globigerinatheka luterbacheri and Globigerinatheka cf. semiinvoluta at 34.3 Ma. A more continuous record is observed for the Early Miocene and the Late Miocene–Early Pliocene where planktic foraminiferal assemblages show a distinct affinity with southern mid- to high-latitude faunas.     

Şerefköy-2, a new Late Miocene mammal locality from the Yatağan Formation,Muğla,SW Turkey

Here we report on a new fossil locality, ?erefköy-2, from the Yata?an Basin of southwestern Turkey that preserves a well-sampled, abundant, and diverse mammal fauna. Indeed, after three field seasons, more than 1200 catalogued specimens representing 26 mammal species belonging to 14 genera make the ?erefköy-2 mammalian assemblage one of the richest Late Miocene fauna from Anatolia. Five hipparionines, six bovids, including the rare and enigmatic Urmiatherium rugosifrons and the presence of Pliohyrax graecus, strongly support affinities with Late Miocene faunas from Samos Island, Greece. Through a consideration of the identified material and the subsequent comparison with material from well-known Balkan and Anatolian faunas, a Middle Turolian (MN12) age for ?erefköy-2 is indicated.     

Snake fauna (Reptilia: Serpentes) from the Early/Middle Miocene of Sandelzhausen and Rothenstein 13 (Germany)

The Early/Middle Miocene (European Land Mammal Zone MN5) localities of Sandelzhausen and Rothenstein 13 in southern Germany have yielded remains of about 13 ophidian taxa: Eoanilius sp. (Aniliidae), Bavarioboa ultima (Boidae), “Coluber” sp., ?Telescopus sp., Natrix sp., cf. Natrix sp., cf. “Neonatrix” sp., unidentified “colubrines” and “natricines” (Colubridae), Naja sp., an unidentified elapid (Elapidae), Vipera sp. (“Oriental viper”), Vipera sp. (“aspis complex”) (Viperidae). Both faunas document a transitional phase from those reported from several late Early and Middle Miocene sites of Central and Western Europe. The climates of Sandelzhausen and Rothenstein 13, as indicated by ophidian fossils, were warm, although not tropical or subtropical.