Mammalian biostratigraphy, geochronology, and zoogeographic relationships of the Late Miocene Maragheh fauna, Iran

Palaeoclimatic and palaeoenvironmental interpretations of the Late Oligocene, Late Miocene–Early Pliocene in the Çankırı-Çorum Basin

Sedimentary and structural evolution of the Eastern South Korea Plateau (ESKP), East Sea (Japan Sea)

Reconstruction of past vegetation and climates in the Cankiri-Corum Basin, one of the largest basins of Central Anatolia, is important for understanding the regional palaeovegetation. In this study, the palaeovegetational and palaeoclimatic proxies of the basin within the late middle Miocene and early Pleistocene interval are presented using the Integrated Plant Record (IPR) vegetation analysis and the coexistence approach (CA). The IPR analysis allows the reconstruction of six types of zonal vegetation: broad-leaved deciduous forests (BLDF), mixed mesophytic forests (MMF), broad-leaved evergreen forests (BLEF), xeric open woodlands and xeric grasslands or steppes, all identified from the microfloras of Cankiri-Corum Basin. During the late middle Miocene, warm temperate and humid climatic conditions prevailed and the palaeovegetation in the Cankiri-Corum Basin was represented by BLEF and an ecotone between MMF and BLEF. The cooling from the late middle Miocene to early late Miocene had begun as well, as low precipitation periods in the climatic conditions during the same time interval were recorded in the basin. Presumably, the proportion of broad-leaved deciduous elements remained balanced because the palaeotopography did not change significantly during the late Miocene in the Cankiri-Corum Basin. The recorded cooling could be related to a global climatic change from the middle to late Miocene. During the Tortonian to Messinian transition, the palaeovegetation type was represented by BLDF and suggests a continuous cooling trend in the basin. The palaeovegetation types of the late late Miocene comprise MMF in the northern part of the Cankiri-Corum Basin and xeric grassland or steppe in the southern part of the basin. Warm and dry climatic conditions were recorded from the Tortonian to the Messinian; these warm conditions during the Messinian could be correlated to the Messinian salinity crisis. According to the IPR analysis results, the northern part of the Cankiri-Corum Basin palaeotopography seems to be higher in altitude than the southern part. Palaeovegetation types in the latest late Miocene and early Pliocene were characterised by MMF and an ecotone between BLDF and MMF in the northern part of the Cankiri-Corum Basin and open woodland vegetation in the southern part of the basin. The percentage of the broad-leaved deciduous component from the latest late Miocene and early Pliocene decreases in the Cankiri-Corum Basin, which could be related to beginning uplift starting changes in the palaeotopography. In the early Pliocene, this uplift was continued in the basin.

Italian Cenozoic crocodilians: taxa, timing and palaeobiogeographic implications

In evolutionary paleontology of terrestrial biotas, the Miocene is the most important age especially for evolution of hominids and mammalian faunas. The modern mammalian fauna appeared from the end of this age in Eurasia. In Sub-Saharan Africa, the assemblage of the late Miocene mammalian faunas was very poor, and these faunas were represented by only few faunas. Therefore, this incompleteness of the late Miocene East African faunas, it is very difficult to analyze faunal turnover of Sub-Saharan mammalian faunas and compare with Eurasian and Sub-Saharan faunas of this age.The paleontological contribution of the Japan and Kenya joint expedition to the Samburu Hills, northern Kenya covered this gap of mammalian evolution in Sub-Saharan Africa.In this work, the Miocene mammalian faunas in Sub-Saharan Africa is examined the half-life (Kurtén 1959, 1972, 1988) of each faunal assemblages (sets).Assemblage of the mammalian faunas from early Miocene was comparatively stable and had long half life in Sub-Saharan Africa on the basis of the results of this work.However, mammalian assemblage changed drastically at the middle Miocene (Astaracian) in Sub-Saharan Africa.A great number of early to middle Miocene mammalian taxa were extinct and the modern mammalian taxa appeared in this period. The half life of middle and late Miocene mammalian faunas is shortened compared with the early Miocene faunas in the East Africa. This geological event of faunal turnover occurred by the immigration and divergence of open land taxa.It is evident that the rise of open land taxa is related to the environmental change for the plateau phonolite and basalt volcanism in the middle Miocene East Africa (Pickford 1981) and the worldwide warm and arid event (savannitisation) of continental temperate zone in the middle to late Miocene (Liu 1988). In the middle Miocene (16 Ma) Pacific region, it has been proposed that the tropical event is recognized from shallow marine faunas of the Southwestern Japan (Tsuchi 1986). African and Eurasian land connection was also established before the middle Miocene (16 Ma±) (Bernor et al. 1987).The Astaracian faunal turnover in Sub-Saharan Africa is considered to be caused by immigration and diversity of open country mammalian taxa and that was related to the worldwide middle Miocene warm event and the plateau volcanism in middle Miocene East Africa. Furthermore, the Pleistocene and modern taxa and their direct ancestors of Sub-Saharan Africa appeared from the late Miocene faunas of East Africa. It has been made clear that the Namurungule Fauna is the forerunner of the modern Sub-Saharan mammalian fauna of savanna environments.As mentioned before, the Hominid Fossil was found from the Namurungule Formation (late Miocene) of northern Kenya. The savannitisation in the Sub-Saharan Africa began in middle Miocene. The origin of hominid bipedalism seems to be closely related to the environmental change from forest to open land (Foley 1984). Human evolution in East Africa is accelerated by the savannitisation of Sub-Saharan Africa which commenced earlier than that of Eurasia and continued throughout the Neogene.

Miocene stratigraphy and mammal fauna from the Sulaiman Range, Southwestern Himalayas, Pakistan

Miocene-Pliocene foraminifera recovered from three subsurface sections in the Yufutsu Oil and Gas Field, southern Hokkaido, are studied in detail to infer paleoceanographic and paleobathymetric implications and to clarify the history of the basin. Foraminiferal faunas indicate a progressive increase in bathymetry from a brackish shallow marine to a bathyal condition during the Middle Miocene. The basin then came under the spell of volcanism and nearly 1000 m of basalt-basaltic andesite flows accumulated until the top of the volcano emerged out of the sea. After the cessation of volcanic activity, the basin subsided and cold bathyal conditions prevailed in which diatomaceous-siliceous sediment was accumulated during the Late Miocene. The periodic episodes of subsidence are inferred to have been related to the genesis of the Japan Sea. The basin witnessed a major hiatus during the Late Miocene-Early Pliocene. During the Late Pliocene, coarse clastic sediments accumulated in the region in a cold bathyal condition of deposition. The clastic sediment is thought to have derived from the eastern upland where the Upper Cretaceous and Paleogene sedimentary rocks were exposed. It is supposed that the hiatus in the Late Miocene-Early Pliocene is a result of an upheaval of central Hokkaido, which unstabilized the sediment and changed bottom current condition.The Early to Middle Miocene microfauna of the region is similar to those of the Japan Sea region, whereas the Late Miocene fauna is different in abundance of agglutinated foraminifera. Such faunal differences between the study area and Japan Sea region of Honshu in the Late Miocene are mainly due to the variable distances from the proto-Tsugaru Strait that let carbonate-saturated Pacific seawater into the Japan Sea.

<p>We present a structural study on late Miocene-early Pliocene out-of-sequence thrusts affecting the southern Apennine chain. The analyzed structures are exposed in the Campania region (southern Italy). Here, leading thrusts bound the N-NE side of the carbonate ridges that form the regional mountain backbone. In several outcrops, the Mesozoic carbonates are superposed onto the unconformable wedge-top basin deposits of the upper Miocene Castelvetere Group, providing constraints to the age of the activity of this thrusting event. We further analyzed the tectonic windows of Giffoni and Campagna, located on the rear of the leading thrust. We reconstructed the orogenic evolution of this part of the orogen. The first was related to the in-sequence thrusting with minor thrusts and folds, widespread both in the footwall and in the hanging wall. A subsequent extension has formed normal faults crosscutting the early thrusts and folds. All structures were subsequently affected by two shortening stages, which also deformed the upper Miocene wedge top basin deposits of the Castelvetere Group. We interpreted these late structures as related to an out-of-sequence thrust system defined by a main frontal E-verging thrust and lateral ramps characterized by N and S vergences. Associated with these thrusting events, LANFs were formed in the hanging wall of the major thrusts. Such out-of-sequence thrusts are observed in the whole southern Apennines and record a thrusting event that occurred in the late Messinian-early Pliocene. We related this tectonic episode to the positive inversion of inherited normal faults located in the Paleozoic basement. These envelopments thrust upward crosscut the allochthonous wedge, including, in the western zone of the chain, the upper Miocene wedge-top basin deposits. Finally, we suggest that the two tectonic windows are the result of the formation of an E-W trending regional antiform, associated with a late S-verging back-thrust, that has been eroded and crosscut by Early Pleistocene normal faults.</p>

A shortage of Cenozoic vertebrate fossils in the Tibetan Plateau has been an obstacle in our understanding of biological evolution in response to changes in tectonism, topography, and environment. This is especially true for Paleogene records, so far known by only two sites along the northern rim of the Plateau. We report a Hongyazi Basin in northern Tibetan Plateau that produces at least three mammalian faunas that span Oligocene through late Miocene. Located at the foothills of the Danghe Nanshan and presently connected to the northern margin of the Suganhu Basin through the Greater Haltang River, the intermountain basin is controlled by the tectonics of the Danghe Nanshan to the north and Chahan’ebotu Mountain to the south, making the basin sediments well suited for inferring the evolutionary history of these two mountain ranges. At the bottom of the local section, the Oligocene Haltang Fauna is best compared to the early Oligocene Desmatolagus-Karakoromys decessus assemblage in the Dingdanggou Fauna in Tabenbuluk Basin. The Middle Miocene Ebotu Fauna from the middle Hongyazi section shares many taxa with the late Middle Miocene Tunggur mammal assemblage in Inner Mongolia, such as Heterosminthus orientalis, Megacricetodon sinensis, Democricetodon lindsayi, and Alloptox gobiensis. Toward the top of the section, the Hongyazi Fauna includes late Miocene elements typical of Hipparion faunas of North China. All three faunas are of typical North China-Central Asian characteristics, suggesting a lack of geographic barriers for faunal differentiation through the late Miocene. Sedimentary packages producing these faunas are arrayed from north to south in progressively younger strata, consistent with a compressive regime to accommodate shortening between Danghe Nanshan and Chahan’ebotu Mountain by thrust faults and folds. With additional constraints from vertebrate fossils along the northern flanks of the Danghe Nanshan, an eastward propagation of the Danghe Nanshan is postulated.

Oceanographic significance of Pacific late miocene calcareous nannoplankton

Over the past 10 million years, coastal-marine settings along the Peruvian Margin have undergone profound geographic and oceanographic transformations, resulting in extensive changes in coastal-marine communities. While mollusk taxonomy research is slowly being integrated into ecosystem-wide analyses, which have historically centered on vertebrates, a long-term chronostratigraphically controlled analysis of molluscan diversity and compositional changes has not been undertaken for this region. We compiled a database covering 152 species, 97 genera, and 51 families of mollusk fossils from the Peruvian Margin (13–16°S) to assess long-term diversification patterns and faunal turnover from the late Miocene to the present. We identified two distinctive molluscan assemblages. The first, dating to the late Miocene (10–6 Ma), underwent a substantial shift during the Mio-Pliocene transition (6–4 Ma), culminating in a second assemblage more akin to modern counterparts. This shift resulted in an increase in diversity, with the younger assemblage (6–0 Ma) exhibiting greater genus richness than the former late Miocene assemblage. The turnover at 6–4 Ma was driven by peaks in bivalve origination (6–5 Ma) along with elevated extinction rates for gastropods (6–5 Ma) and bivalves (5–4 Ma). Ecological analyses revealed that no single ecological trait consistently changed during this interval, indicating that the turnover resulted from a broad reorganization of ecological strategies. We propose that the major molluscan turnover during the late Miocene–early Pliocene is associated with geomorphological changes related to the Andean uplift, the disappearance of semi-embayments, and a sea-level rise.

The paleomagnetic stratigraphy, biostratigraphy, and paleoclimatology have been studied in two marine sections of late Miocene to early Pliocene age in New Zealand. A total of over 850 separately oriented cores were collected from 270 sites. The Blind River section (41°43′ S.) is now adjacent to the southernmost subtropical (temperate) water mass, but planktonic foraminifera indicate that the area was covered by subantarctic water during much of late Miocene and early Pliocene time. The Mangapoike River section (38°55′ S.) records temperature oscillations mainly within the subtropical water mass during late Miocene–early Pliocene age, with perhaps one subantarctic interval during latest Miocene time. The Miocene-Pliocene boundary in New Zealand has consistently been placed at the first evolutionary appearance of Globorotalia puncticulata at the boundary between the late Miocene Kapitean Stage and the early Pliocene Opoitian Stage. This boundary lies within sediments deposited during the Gilbert Reversed Epoch between the Nunivak Event (base at 4.14 m.y. B.P.) and the Gilbert C Event (top at 4.33 m.y. B.P.) in both sections. Thus, the Miocene-Pliocene boundary, as recognized in New Zealand, is dated as 4.3 ± 0.1 m.y., which appears to be slightly younger than the type (International) Miocene-Pliocene boundary in Italy (4.9 to 5.1 m.y.). Biostratigraphic ranges of planktonic foraminifera between New Zealand and the Mediterranean differ in detail, perhaps due to different paleo-oceanographic histories. A major cooling episode during the early Gilbert Reversed Epoch is recorded at Blind River and Mangapoike River. This cooling is more pronounced in the southern section examined, where it is represented by the occurrence of a central subantarctic planktonic foraminiferal assemblage. In the northern section, cooling was also pronounced, although of shorter duration, represented by a probably northern subantarctic assemblage. The Miocene-Pliocene boundary in Europe has still only been dated indirectly by means of non-Mediterranean sections. Interpretation of late Cenozoic paleomagnetic data from Mediterranean deep-sea cores collected from Glomar Challenger is rejected.

<p>The late Miocene-early Pliocene geology of the Makara and Ruakokoputuna Valleys in the northern Aorangi Range, south-east Wairarapa, is described in detail. In this area, a succession of Neogene sedimentary units laps onto basement rocks of Cretaceous age, and late Miocene-early Pliocene stratigraphy varies markedly, from bathyal mudstone to high energy coastal environments, over distances of only a few kilometres. Sections were measured at four key locations, which provided reference sites for stratigraphic changes across the study area. Additional detailed field mapping was carried out around Te Ahitaitai Ridge. Depositional environments were interpreted using grain size analysis, macrofossil and foraminiferal assemblages, and palynology. Foraminiferal biostratigraphy was used to constrain the ages of samples. Data obtained by these methods were combined with previous authors’ work to produce a synthesis map, unit correlations, and geological cross-sections of the Makara and Ruakokoputuna Valleys. Late Miocene-early Pliocene geological history is interpreted, and a depositional model is proposed to explain the presence of giant cross-beds in the Clay Creek Limestone. Despite major differences in lithology, the Clay Creek Limestone and Bells Creek Mudstone are shown to be partially laterally equivalent, while the overlying Makara Greensand is shown to be a diachronous unit which ranges from late Miocene (Kapitean) to early Pliocene (Opoitian) in age. This revised stratigraphy raises questions about the current classification of the Palliser and Onoke Groups, and provides new insights into regional geological history. The late Miocene-early Pliocene stratigraphy records a history of regional subsidence, punctuated by episodes of deformation which caused localised uplift and erosion. Previous seismic imaging studies identified one such episode of accelerated crustal shortening and deformation in the Wairarapa region near the Miocene-Pliocene boundary. The Clay Creek Limestone has proven to be a useful marker horizon for constraining the timing and style of deformation, which is interpreted to have occurred prior to 7.2 Ma. Major differences in stratigraphy between the upthrown and downthrown sides of the Mangaopari Fault indicate that the fault was active during this deformational episode. Lithostratigraphic units from the study area have been correlated with units in other parts of the Wairarapa, and these correlations suggest that late Miocene deformation in the region may have propagated from south to north.</p>

<p>The late Miocene-early Pliocene geology of the Makara and Ruakokoputuna Valleys in the northern Aorangi Range, south-east Wairarapa, is described in detail. In this area, a succession of Neogene sedimentary units laps onto basement rocks of Cretaceous age, and late Miocene-early Pliocene stratigraphy varies markedly, from bathyal mudstone to high energy coastal environments, over distances of only a few kilometres. Sections were measured at four key locations, which provided reference sites for stratigraphic changes across the study area. Additional detailed field mapping was carried out around Te Ahitaitai Ridge. Depositional environments were interpreted using grain size analysis, macrofossil and foraminiferal assemblages, and palynology. Foraminiferal biostratigraphy was used to constrain the ages of samples. Data obtained by these methods were combined with previous authors’ work to produce a synthesis map, unit correlations, and geological cross-sections of the Makara and Ruakokoputuna Valleys. Late Miocene-early Pliocene geological history is interpreted, and a depositional model is proposed to explain the presence of giant cross-beds in the Clay Creek Limestone. Despite major differences in lithology, the Clay Creek Limestone and Bells Creek Mudstone are shown to be partially laterally equivalent, while the overlying Makara Greensand is shown to be a diachronous unit which ranges from late Miocene (Kapitean) to early Pliocene (Opoitian) in age. This revised stratigraphy raises questions about the current classification of the Palliser and Onoke Groups, and provides new insights into regional geological history. The late Miocene-early Pliocene stratigraphy records a history of regional subsidence, punctuated by episodes of deformation which caused localised uplift and erosion. Previous seismic imaging studies identified one such episode of accelerated crustal shortening and deformation in the Wairarapa region near the Miocene-Pliocene boundary. The Clay Creek Limestone has proven to be a useful marker horizon for constraining the timing and style of deformation, which is interpreted to have occurred prior to 7.2 Ma. Major differences in stratigraphy between the upthrown and downthrown sides of the Mangaopari Fault indicate that the fault was active during this deformational episode. Lithostratigraphic units from the study area have been correlated with units in other parts of the Wairarapa, and these correlations suggest that late Miocene deformation in the region may have propagated from south to north.</p>

Interpretations of seismic, gravity and magnetic anomalies and structural data on the coastal zone of southern part of Central Viet Nam (SCVN) and the adjacent Tertiary basins suggest several phases in the tectonic evolution of the study region since the Late Cretaceous to Quaternary. In this paper, we try to clarify the tectonic evolution of SCVN and the adjacent continental margin. The Cretaceous – Paleocene tectonic phase commenced after cessation of the West Pacific plutonic magmatic activity that produced numerous diabases and aplite dykes of mainly sub-meridian orientation. It was characterized by N–S compression and E–W extension. The geomorphology and geology ofSE Asiawere considerably changed during the Neotectonic phases caused by collision between the Indian plate and the Eurasian continent. Two tectonic phases – Early and Late Neotectonic – are separated by a regional unconformity represented by a boundary surface between below strongly deformed strata (synrift) and above less deformed formations (post-rift). The Early Neotectonic phase was related to the left-lateral movement of the Red River Fault Zone (RRFZ) and includes two tectonic sub-phases: Eocene – Oligocene (NW–SE compression), and Oligocene – Miocene (E–W compression). Activity in the Oligocene-Miocene sub-phase gave birth to rift basins in the continental margin of the SCVN. The Late Neotectonic phase began since the RRFZ stopped left-lateral movement and the East Viet Nam (orSouth China) Sea stopped spreading. The Late Neotectonic phase is also divided into two tectonic sub-phases: Late Early Miocene (sub-meridian compression), and Late Miocene – Pliocene (NE–SW compression). The Late Miocene – Pliocene sub-phase is characterized by vertical movements that caused episodic uplifting of the onland terrains, and subsidence of the offshore Phu Khanh basin. Besides, Miocene – Pliocene-Quarternary basaltic eruptions were widespread all over the southern Indosinian terrain and the continental margin.