Search results for " Triassic"

Triasina hantkeni limestones from western Sicily

2010

4D paleoenvironmental evolution of the Early Triassic Sonoma Foreland Basin (western USA)

2017

In the wake of the Mesozoic, the Early Triassic (~251.95 Ma) corresponds to the aftermath of the most severe mass extinction of the Phanerozoic: the end-Permian crisis, when life was nearly obliterated (e.g., 90% of marine species disappeared). Consequences of this mass extinction are thought to have prevailed for several millions of years, implying a delayed recovery lasting the whole Early Triassic, if not more. Several paradigms have been established and associated to a delayed biotic recovery scenario expected to have resulted from harsh and deleterious paleoenvironments. These paradigms include a global anoxia in the marine realm, a “Lilliput” effect, and the presence of “disaster” tax…

Hypercalcified sponges from the Upper Triassic (Norian-Rhaetian) reefs of Sicily

2015

The sponge-dominated Upper Triassic (Norian-Rhaetian) reefs of Sicily yielded the most abundant hypercalcified sponge taxa compared with other time equivalent reefs in the world. Chambered sponges (“Sphinctozoa”) are the most abundant group among the hypercalcified sponges. All together almost 150 species of hypercalcified sponges (including sphinctozoans, inozoans, chaetetids, disjectoporids and spongiomorphids) were recognized in the Norian-Rhaetian reefs occurring in different localities in Sicily. 93 species (30 new, 28 as sp. indet.) of sphinctozoans, belonging to 18 families (2 new: Polytubithalamiidae, Globucatenulaiidae) and 35 genera (4 new: Globucatenula, Polytubithalamia, Rostros…

Integrated stratigraphy of the Norian GSSP candidate Pizzo Mondello section (Sicani Mountains, Sicily)

2008

Synsedimentary-tectonic, soft-sediment deformation and volcanism in the rifted Tethyan margin from the Upper Triassic–Middle Jurassic deep-water carb…

2014

Abstract The Pizzo Lupo section (Sicanian Mts, central Sicily) is an Upper Triassic–Lower Jurassic condensed deep-water succession, where the relationships among synsedimentary tectonic, soft-sediment deformations, volcanism and lithological changes reflect the evolution of a rift-basin. The morphostructural setting of the studied basin appears as a gently dipping slope where a fault-delimited area (graben to halfgraben) was developed. The instability of the sea floor, related to the seismic shocks, was the cause of the gravity-driven deformational sedimentary structures (slumping, breccia channelized bodies). The partly stratified basaltic rocks, with disorganized and chaotic stratificatio…

The evolutionary trend of platform denticulation in Middle Triassic acuminate Gondolellidae (Conodonta)

2017

Kılıç, Ali Murat (Balikesir Author)

On the origin of the southern Permian Basin, Central Europe.

2000

A detailed study of the structural and stratigraphic evolution of the Southern Permian Basin during latest Carboniferous to Early Jurassic times, supported by quantitative subsidence analyses and forward basin modelling for 25 wells, leads us to modify the conventional model for the Rotliegend-Zechstein development of this basin. The Late Permian-Early Jurassic tectonic subsidence curves are typical for a Permian to Early Triassic extensional stage that is followed by thermal subsidence. However, a purely extensional model is extremely problematic because active faulting during this time is 'minor' and generally hard to document. Using inverse techniques to model the subsidence curves, we q…

The revision of Pinacoceras (Ammonoidea, Upper triassic) of the Gemmellaro Collection.

2010

New data on the Upper Triassic reefs of Western Sicily: stratigraphic constraints for the paleogeographic reconstruction of the Sicanian and Trapanes…

2005

Early Triassic proliferation of microbial deposit

2019

International audience; In modern examples of well-developed microbial-dominated deposits associated with metazoan organisms can be currently found in various environments including but not restricted to lagoons in Polynesia (Sprachta et al., 2001), the warm water of the Cuba (e.g., Bouton et al., 2016; Pace et al., 2018), the hypersaline lakes of the Great Salt Lake (USA; e.g., Bouton et al., 2016; Vennin et al., 2019; Vanden Berg, 2019), or the alkaline Satonda Crater Lake in Indonesia (Arp et al., 2003; Satuyana et al., 2010). In Early Triassic, several authors indicated that microbial deposits are frequently associated with sponges, bivalves, brachiopods, ostracods and echinoderms and d…