Search results for "14"
showing 10 items of 9841 documents
The end of the Messinian salinity crisis: Evidences from the Chelif Basin (Algeria).
2007
How did the Messinian Salinity Crisis end is a matter of intense debate between two opposite concepts i.e., the generalised dilution event, the so-called Lago–Mare, followed by the sudden restoration of the marine conditions at the base of the Zanclean, or the early partial or complete marine refill that would have happened earlier during the upper Messinian. The Chelif Basin of Northwestern Algeria, one of the greatest Messinian marginal basins of the Mediterranean, provides an exceptional opportunity to study in detail how this major paleoenvironmental change occurred through continuous sedimentary records of the Miocene–Pliocene boundary. Five sections representative of both the central …
Smithian shoreline migrations and depositional settings in Timpoweap Canyon (Early Triassic, Utah, USA).
2014
AbstractIn Timpoweap Canyon near Hurricane (Utah, USA), spectacular outcrop conditions of Early Triassic rocks document the geometric relationships between a massive Smithian fenestral-microbial unit and underlying, lateral and overlying sedimentary units. This allows us to reconstruct the evolution of depositional environments and high-frequency relative sea-level fluctuations in the studied area. Depositional environments evolved from a coastal plain with continental deposits to peritidal settings with fenestral-microbial limestones, which are overlain by intertidal to shallow subtidal marine bioclastic limestones. This transgressive trend of a large-scale depositional sequence marks a lo…
Climatic fluctuations and seasonality during the Late Jurassic (Oxfordian–Early Kimmeridgian) inferred from delta18O of Paris Basin oyster shells.
2008
10 pages; International audience; Oxygen isotope data from biostratigraphically well-dated oyster shells from the Late Jurassic of the eastern Paris Basin are used to reconstruct the thermal evolution of western Tethyan surface waters during the Early Oxfordian–Early Kimmeridgian interval. Seventy eight oyster shells were carefully screened for potential diagenetic alteration using cathodoluminescence microscopy. Isotope analyses were performed on nonluminescent parts of shells (n=264). Intra-shell δ18O variability was estimated by microsampling along a transect perpendicular to the growth lines of the largest oyster shell. The sinusoidal distribution of the δ18O values along this transect …
Middle Triassic sharks from the Catalan Coastal ranges (NE Spain) and faunal colonization patterns during the westward transgression of Tethys
2020
Abstract Palaeogeographic changes that occurred during the Middle Triassic in the westernmost Tethyan domain were governed by a westward marine transgression of the Tethys Ocean. The transgression flooded wide areas of the eastern part of Iberia, forming new epicontinental shallow-marine environments, which were subsequently colonized by diverse faunas, including chondrichthyans. The transgression is recorded by two successive transgressive–regressive cycles: (1) middle–late Anisian and (2) late Anisian–early Carnian. Here, we describe the chondrichthyan fauna recovered from several Middle Triassic stratigraphic sections (Pelsonian-Longobardian) located at the Catalan Coastal Basin (western…
Palynofacies and calcareous nannofossils in the Upper Kimmeridgian, southeastern Paris basin (France)
2005
AbstractThe Upper Kimmeridgian Members “Calcaires blancs supérieurs” and the “Marnes à exogyres supérieures” of the southeastern Paris basin were investigated for their palynofacies and calcareous nannofossils. These members display alternating limestone-marl lithotypes and represent shallow marine palaeoenvironments. The lower carbonate member is interpreted as a proximal palaeoenvironment (palaeobathymetry = 5 to 10 m), where storm and swell deposits were prevalent and the salinity was occasionally weak. The relative richness of brown phytoclasts in this part is favoured by good preservation related to restricted conditions. These conditions would explain the dominance of the nannofoss…
First report of Gogia (Eocrinoidea, Echinodermata) from the Early-Middle Cambrian of Sonora (Mexico), with biostratigraphical and palaeoecological co…
2009
10 pages; International audience; The blastozoan echinoderm genus Gogia is reported for the first time in the Early and the Middle Cambrian of Mexico. Reports in different members of the section of San José de Gracia (Sonora State, northwestern Mexico) extend the palaeogeographical range of the genus to the South Laurentia, and the stratigraphic range of Gogia granulosa to the whole first half of middle Middle Cambrian. Isolated plates occur in rocks deposited in detrital inner platform and complete specimens, in carbonate outer platform, confirming their ability to live in diverse environments. Their presence in these different environments through the Early-Middle Cambrian on Laurentia ag…
Pseudoskirroceras, a remarkable but poorly known Early Pliensbachian Tethyan ammonite genus: New data from the High Atlas (Morocco).
2007
13 pages; International audience; The discovery of new Early Pliensbachian ammonite faunas in Central High Atlas (Morocco) allows the re-examination of the taxonomic, stratigraphical and palaeogeographical framework of the genus Pseudoskirroceras, an intriguing but until now poorly known Tethyan taxon. For the first time, several specimens of Pseudoskirroceras mastodon (Fucini, 1935) the type species of the genus, have been collected in a well-known stratigraphical context. This material allows the evaluation of intra-specific variability and consequently the assessment of the taxonomical relevance of various geometrical and ornamental features. The best diagnostic features are the clearly …
COMMENT TO LEHRMANN ET AL. NEW SECTIONS AND OBSERVATIONS FROM THE NANPANJIANG BASIN, SOUTH CHINA
2016
In the study of Earth-surface environmental processes during the events associated with the Permian–Triassic boundary, a key issue is the nature of the latest Permian pre-extinction surface in shallow marine limestones in numerous sites, principally within the Tethyan realm. Sediments below this surface pre-date the extinction event, so that the limestones comprising these latest Permian facies contain diverse fossil remains of organisms that lived just before the extinction. At all reported sites, this surface is disconformably overlain by post-extinction sediments, which contain microbialites in many places, particularly in Tethys. The nature of the youngest pre-extinction surface remains…
Using growth and geochemical composition of Clathromorphum compactum to track multiscale North Atlantic hydro-climate variability
2020
International audience; Records of ocean/atmosphere dynamics over the past centuries are essential to understand processes driving climate variability. This is particularly true for the Northwest Atlantic which is a key region with an essential role in global climate regulation. Over the past two decades, coralline red algae have been increasingly used as environmental and climatic archives for the marine realm and hold the potential to extend long-term instrumental measurements. Here, we investigate the possibility to extract climate and environmental information from annual growth patterns and geochemical composition of the coralline red algae, Clathromorphum compactum, from Saint-Pierre …
2020
Skeletal remains in archaeological strata are often assumed to be of similar ages. Here we show that combined Sr and O isotope analyses can serve as a powerful tool for assessing fish provenance and even for identifying fossil fish teeth in archaeological contexts. For this purpose, we established a reference Sr and O isotope dataset of extant fish teeth from major water bodies in the Southern Levant. Fossil shark teeth were identified within Iron Age cultural layers dating to 8–9th century BCE in the City of David, Jerusalem, although the reason for their presence remains unclear. Their enameloid 87Sr/86Sr and δ18OPO4 values [0.7075 ± 0.0001 (1 SD, n = 7) and 19.6 ± 0.9‰ (1 SD, n = 6), res…