No abstract

No abstract

No abstract

International audienceThe Turkish part of the Tethyan realm is represented by a series of terranes juxtaposed through Alpine convergent movements and separated by complex suture zones. Different terranes can be defined and characterized by their dominant geological background. The Pontides domain represents a segment of the former active margin of Eurasia, where back-arc basins opened in the Triassic and separated the Sakarya terrane from neighbouring regions. Sakarya was re-accreted to Laurasia through the Balkanic mid-Cretaceous orogenic event that also affected the Rhodope and Strandja zones. The whole region from the Balkans to the Caucasus was then affected by a reversal of subduction and creation of a Late Cretaceous arc before collision with the Anatolian domain in the Eocene. If the Anatolian terrane underwent an evolution similar to Sakarya during the Late Paleozoic and Early Triassic times, both terranes had a diverging history during and after the Eo-Cimmerian collision. North of Sakarya, the Küre back-arc was closed during the Jurassic, whereas north of the Anatolian domain, the back-arc type oceans did not close before the Late Cretaceous. During the Cretaceous, both domains were affected by ophiolite obduction, but in very different ways: north directed diachronous Middle to Late Cretaceous mélange obduction on the Jurassic Sakarya passive margin; Senonian synchronous southward obduction on the Triassic passive margin of Anatolia. From this, it appears that the Izmir-Ankara suture, currently separating both terranes, is composite, and that the passive margin of Sakarya is not the conjugate margin of Anatolia. To the south, the Cimmerian Taurus domain together with the Beydağları domain (part of the larger Greater Apulian terrane), were detached from north Gondwana in the Permian during the opening of the Neotethys (East-Mediterranean basin). The drifting Cimmerian blocks entered into a soft collision with the Anatolian and related terranes in the Eo-Cimmerian orogenic phase (Late Triassic), thus suturing the Paleotethys. At that time, the Taurus plate developed foreland-type basins, filled with flysch-molasse deposits that locally overstepped the lower plate Taurus terrane and were deposited in the opening Neotethys to the south. These olistostromal deposits are characterized by pelagic Carboniferous and Permian material from the Paleotethys suture zone found in the Mersin mélange. The latter, as well as the Antalya and Mamonia domains are represented by a series of exotic units now found south of the main Taurus range. Part of the Mersin exotic material was clearly derived from the former north Anatolian passive margin (Huğlu-type series) and re-displaced during the Paleogene. This led us to propose a plate tectonic model where the Anatolian ophiolitic front is linked up with the Samail/Baër-Bassit obduction front found along the Arabian margin. The obduction front was indented by the Anatolian promontory whose eastern end was partially subducted. Continued slab roll-back of the Neotethys allowed A...

No abstract

No abstract

The time span between the Variscan and Alpine cycles is not devoid of any major tectonic activity, and corresponds to the Cimmerian cycle. Between the Early Permian and Late Triassic, the Eocimmerian cycle was marked by the closure of Palaeotethys and opening of Neotethys and of an array of south Eurasian back-arc basins. This was followed by the break-up of Pangaea and the Early Jurassic opening of the central Atlantic and Alpine Tethys. However, in the area of the Eocimmerian collision, the geodynamic evolution is relatively uninfluenced by this event, and a new cycle of Cimmerian deformation affected the Hellenides, Dinarides, Balkans and Pontides in Jurassic-Early Cretaceous times. The anti-clockwise rotation of Africa during the Late Cretaceous heralded the onset of Alpine orogenic processes, characterized first by major east-west shortening, and opening and closure of younger oceanic basins of back-arc type.

Conchostracans or clam shrimp (order Conchostraca Sars) are arthropods with a carapace consisting of two chitinous lateral valves. Triassic conchostracans range in size from 2 to 12.5 mm long and are common in deposits that formed in fresh water lakes, isolated ponds and brackish areas. Their dessication- and freeze-resistant eggs can be dispersed by wind over long distances. Therefore many conchostracan species are distributed throughout the entire northern hemisphere. In the Late Permian to Middle Triassic interval, several of these forms are also found in Gondwana. Many wide-ranging conchostracan species have short stratigraphic ranges, making them excellent guide forms for subdivision of Triassic time and for long-range correlations. The stratigraphic resolution that can be achieved with conchostracan zones is often as high as for ammonoid and conodont zones found in pelagic marine deposits. This makes conchostracans the most useful group available for biostratigraphic subdivision and correlation in continental lake deposits. Upper Triassic Gondwanan conchostracan faunas are different from conchostracan faunas of the northern hemisphere. In the Norian, some slight provincialism can be observed even within the northern hemisphere. For example, the Sevatian Redondestheria seems to be restricted to North America and Acadiestheriella n. gen. so far has been found only in the Sevatian deposits from the Fundy Basin of southeastern Canada. Here we establish a conchostracan zonation for the Changhsingian (Late Permian) to Hettangian (Early Jurassic) of the northern hemisphere that, for the most part, is very well correlated with the marine scale. This zonation is especially robust for the Changhsingian to early Anisian, late Ladinian to Cordevolian and Rhaetian to Hettangian intervals. For most of the Middle and Upper Triassic, this zonation is still preliminary. Five new genera, six new species and a new subspecies of conchostracans are described that are stratigraphically important.