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NARROW
GeoRef Subject
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all geography including DSDP/ODP Sites and Legs
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Paragloborotalia opima
Middle Eocene to Middle Miocene planktonic foraminiferal biostratigraphy for internal basins (Monferrato and northern Apennines, Italy)
TAXONOMY, BIOSTRATIGRAPHY, AND PHYLOGENY OF OLIGOCENE AND EARLY MIOCENE PARAGLOBOROTALIA AND PARASUBBOTINA
ABSTRACT The taxonomy, phylogeny, and biostratigraphy of Oligocene and early Miocene Paragloborotalia and Parasubbotina are reviewed. The two genera are closely related; Paragloborotalia was derived from Parasubbotina in the early Eocene. Parasubbotina was more diverse during the middle Eocene, while Paragloborotalia experienced considerable diversification during the mid-Oligocene and in the latest Oligocene-earliest Miocene. A significant finding has been the synonymization of Globorotalia ( Tuborotalia ) mendacis Blow, and Turborotalia primitiva Brönnimann and Resig with Globorotalia birnageae Blow. The following species from the time interval of interest are regarded as valid: Paragloborotalia acrostoma (Wezel), Paragloborotalia birnageae (Blow), Paragloborotalia continuosa (Blow), Paragloborotalia incognita (Walters) Paragloborotalia kugleri (Bolli), Paragloborotalia mayeri (Cushman and Ellisor), Paragloborotalia nana (Bolli), Paragloborotalia opima (Bolli), Paragloborotalia pseudocontinuosa (Jenkins), Paragloborotalia pseudokugleri (Blow), Paragloborotalia semivera (Hornibrook), Paragloborotalia siakensis (LeRoy), Parasubbotina hagni (Gohrbandt), and Parasubbotina varianta (Subbotina). Paragloborotalia is a long-lived group of planktonic foraminifera that spanned the early Eocene to late Miocene and provided the root stock for the evolution of multiple smooth, nonspinose, and keeled globorotaliid lineages during the Neogene. The early Oligocene forms of Paragloborotalia (nana, opima, siakensis, pseudocontinuosa ) have 4 or 5 globular chambers in the final whorl with radial spiral sutures and a broadly rounded periphery. A trend from radial to curved spiral sutures is observed in late Oligocene and earliest Miocene lineages. Most species of Paragloborotalia had wide distributions, but some were more common in tropical to warm subtropical waters (e.g., siakensis, kugleri ) and were especially dominant in the equatorial Pacific divergence zone (e.g., nana, opima, and pseudocontinuosa ) analogous to modern tropical upwelling Neogloboquadrina. Other species thrived in cool subtropical and temperate waters (e.g., acrostoma, incognita ).
Oligocene biozones in correlation with standard zonation ( Martini, 1971 ; ...
(A, B) Catapsydrax dissimilis . Depth: 4605–4610 m (15,108–15,124 ft), Bur...
Distribution and relative abundance of benthic foraminiferal species across...
ERRATA
Planktic/benthic index, benthic foraminiferal indices, and relative abundan...
SEM images of selected Oligocene planktonic foraminifera from the NKK-1 bor...
Oligocene Planktic Foraminiferal Taxonomy and Evolution: An Illustrated Revision of Ocean Drilling Program Site 803
Biostratigraphy and sequence stratigraphy of the Oligocene succession, offshore Nile Delta, southeastern Mediterranean, Egypt, and its paleoenvironmental implications
Nukhul Formation in Wadi Baba, southwest Sinai Peninsula, Egypt
Electron microscope images of planktonic foraminifera from the upper Eocene...
A REVISED TROPICAL TO SUBTROPICAL PALEOGENE PLANKTONIC FORAMINIFERAL ZONATION
TAXONOMY AND STABLE ISOTOPE PALEOECOLOGY OF WELL-PRESERVED PLANKTONIC FORAMINIFERA FROM THE UPPERMOST OLIGOCENE OF TRINIDAD
Oligocene–Miocene basin evolution in SE Anatolia, Turkey: Constraints on the closure of the eastern Tethys gateway
Abstract The Oligocene–Miocene was a time characterized by major climate changes as well as changing plate configurations. The Middle Miocene Climate Transition (17 to 11 Ma) may even have been triggered by a plate tectonic event: the closure of the eastern Tethys gateway, the marine connection between the Mediterranean and Indian Ocean. To address this idea, we focus on the evolution of Oligocene and Miocene foreland basins in the southernmost part of Turkey, the most likely candidates to have formed this gateway. In addition, we take the geodynamic evolution of the Arabian–Eurasian collision into account. The Muş and Elazığ basins, located to the north of the Bitlis–Zagros suture zone, were most likely connected during the Oligocene. The deepening of both basins is biostratigraphically dated by us to occur during the Rupelian (Early Oligocene). Deep marine conditions (between 350 and 750 m) prevailed until the Chattian (Late Oligocene), when the basins shoaled rapidly to subtidal/intertidal environment in tropical to subtropical conditions, as indicated by the macrofossil assemblages. We conclude that the emergence of this basin during the Chattian severely restricted the marine connection between an eastern (Indian Ocean) and western (Mediterranean) marine domain. If a connection persisted it was likely located south of the Bitlis–Zagros suture zone. The Kahramanmaraş basin, located on the northern Arabian promontory south of the Bitlis–Zagros suture zone, was a foreland basin during the Middle and Late Miocene, possibly linked to the Hatay basin to the west and the Lice basin to the east. Our data indicates that this foreland basin experienced shallow marine conditions during the Langhian, followed by a rapid deepening during Langhian/Serravallian and prevailing deep marine conditions (between 350 and 750 m) until the early Tortonian. We have dated the youngest sediments underneath a subduction-related thrust at c . 11 Ma and suggest that this corresponds to the end of underthrusting in the Kahramanmaraş region, i.e. the end of subduction of Arabia. This age coincides in time with the onset of eastern Anatolian volcanism, uplift of the East Anatolian Accretionary Complex, and the onset of the North and East Anatolian Fault Zones accommodating westward escape tectonics of Anatolia. After c . 11 Ma, the foreland basin south of the Bitlis formed not (or no longer) a deep marine connection along the northern margin of Arabia between the Mediterranean Sea and the Indian Ocean. We finally conclude that a causal link between gateway closure and global climate change to a cooler mode, recorded in the Mi3b event (δ 18 O increase) dated at 13.82 Ma, cannot be supported.