Results 251 to 260 of about 31,001 (301)
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Late Miocene Desiccation of the Mediterranean
Nature, 1973This article presents evidence that the Mediterranean Sea was a desiccated deep basin some 6 million years ago.
K. J. HSÜ, W. B. F. RYAN, M. B. CITA
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Phylogenetic analysis of Middle-Late Miocene apes
Journal of Human Evolution, 2022Despite intensive study, many aspects of the evolutionary history of great apes and humans (Hominidae) are not well understood. In particular, the phylogenetic relationships of many fossil taxa remain poorly resolved. This study aims to provide an updated hypothesis of phylogenetic relationships for Middle-Late Miocene fossil apes, focusing on those ...
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On late miocene abyssal hydrography
Marine Micropaleontology, 1981Abstract This contribution is a summary of our studies on late Miocene isotope stratigraphy. We interpret the results using simple models and present additional evidence that the δ 13 C shift at 6.2 Ma was a time-stratigraphic event. The average deep-water metabolic CO 2 and nutrient content remained unchanged across the δ 13 C shift, but the net ...
Michael L. Bender, David W. Graham
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Bone Smashing by Late Miocene Hominidae
Nature, 1968Bones found in the Upper Miocene Fossil Beds of Fort Ternan, Kenya, show evidence of having been broken up by some kind of blunt instrument.
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Postcranial evidence of late Miocene hominin bipedalism in Chad
Nature, 2022Bipedal locomotion is one of the key adaptations that define the hominin clade. Evidence of bipedalism is known from postcranial remains of late Miocene hominins as early as 6 million years ago (Ma) in eastern Africa1-4. Bipedality of Sahelanthropus tchadensis was hitherto inferred about 7 Ma in central Africa (Chad) based on cranial evidence5-7.
G. Daver +8 more
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A Lakeland Area in the Late Miocene
2011Fossil plants recovered from the Late Miocene (Messinian) Hreðavatn-Stafholt Formation grew in a landscape dominated by lakes of different sizes that were connected by small rivers and swampland. Well-drained areas bordering these wetlands were covered by mixed broadleaved deciduous and conifer forests dominated by Pinaceae, Rosaceae, and Acer.
Thomas Denk +3 more
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Late Miocene drying of central Australia
Palaeogeography, Palaeoclimatology, Palaeoecology, 2019Abstract A back to the future approach to climate change refines Neogene records of paleoclimatic cooling and drying as future climate states for a warming world. Near Alcoota station in central Australia is a late Miocene fossil mammal site for Alcoota (10 Ma) and Ongeva (8 Ma) local faunas.
Xuegang Mao, Gregory Retallack
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Late Miocene vegetation of the Pannonian Basin
Palaeogeography, Palaeoclimatology, Palaeoecology, 2017Abstract The Pannonian Basin system provides sufficient data to study local and regional vegetation in the context of palaeoclimate and palaeogeography. The present study attempts to make use of the latest results in stratigraphy and track vegetation change throughout the Late Miocene. Vegetation layers are reconstructed for five time slices, from 10.
Torsten Utescher +3 more
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Late Miocene Pockmarks in the Danish Central Graben - Origin and Significance
68th EAGE Conference and Exhibition incorporating SPE EUROPEC 2006, 2006Late Miocene pockmarks have been identified and mapped in 3D seismic surveys covering large parts of the Danish Central Graben. The upper Miocene succession comprises a thick westward progradational wedge of clay, silt and sand grade siliciclastic sediments. The majority of the pockmarks are located in the clay prone toesets.
Andresen, K. +2 more
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ASTROCHRONOLOGY OF LATE MIDDLE MIOCENE MEDITERRANEAN SECTIONS
2004High-resolution cyclostratigraphy and calcareous plankton astrobiochronology have been obtained from the latest Langhian to the earliest Tortonian of the Mediterranean. The investigated areas (Malta, Tremiti, and Sicily) are located in different geological settings, and the three studied sections show different cyclicity. Direct correlation between the
Iaccarino, SM +11 more
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