Organic geochemistry in a sequence stratigraphic framework. The siliciclastic shelf environment of Cretaceous series, SE France

For a better understanding of siliciclastic shelf environments, correlation between sequence stratigraphy and organic geochemistry is used. Our study is focused on the Cretaceous deposits of Marcoule (Gard, France), particularly on a close-packed siltites layer (200–400 m thick), which is well characterized as a marine flooding facies of a single trangressive–regressive cycle. During the Uppermost Albian and the Lower Cenomanian, the stratigraphic data indicate a change in the depositional environment from offshore to shoreface. Organic geochemistry is used in order to characterize origin and variability of the organic matter in relation to the stratigraphic data. The study is carried out on core samples from 2 drill holes (MAR 203 and MAR 501). Analyses of the aliphatic and aromatic hydrocarbons were performed using GC–MS and focused on biomarker distributions. The biomarkers indicate a contribution of mixed terrestrial and marine organic matter. The changes in molecular signatures are related to variations in the source of organic matter (marine versus terrestrial), preservation conditions (largely influenced by clay and early diagenesis), environmental oxidation-reduction and acidic conditions as well as bioturbation. Various environmental zones, characterized by different molecular signatures, can be distinguished. Resin derived biomarkers can be assigned to higher plant material input and may reflect the evolution and diversity of Gymnospermae versus Angiospermae during the transgressive/regressive cycle. The relative sea-level variations are clearly correlated with the nature and the preservation of the organic matter. For example, the Pr/Ph and Pr/n-C₁₇ ratios as well as the regular steranes distributions underline the maximum flooding surface evidenced by other studies. We observe a good correlation between the organic data and sequence stratigraphy: changes in geochemical signatures reflect the 3rd order depositional cycles.     

Enregistrements sismologiques de l'explosion sur le site de l'usine AZF (Toulouse,France)Seismological records of an explosion at the AZF chemical complex in Toulouse,France

This study presents a detailed analysis of the seismic records of a strong explosion that occurred on 21 September 2001 at a chemical complex located south of Toulouse, France, and provoked important damages. The explosion, which is equivalent to a 3.4 magnitude earthquake, has been recorded at most of the stations of the National Seismological Network, as well as at a station under test at the ‘Observatoire Midi-Pyrénées’, 4.2 km away from the epicentre. The main seismic phases are interpreted using the known crustal structures, and a modelling with synthetic seismograms is performed. To cite this article: A. Souriau et al., C. R. Geoscience 334 (2002) 155–161.     

A model for coupled fluid-flow and mixed-volatile mineral reactions with applications to regional metamorphism

The effect of fluid flow on mixed-volatile reactions in metamorphic rocks is described by an expression derived from the standard equation for coupled chemical-reaction and fluid-flow in porous media. If local mineral-fluid equilibrium is assumed, the expression quantitatively relates the time-integrated flux at any point in a flow-system to the progress of devolatilization reactions and the temperature- and pressure-gradients along the direction of flow. Model calculations indicate that rocks are generally devolatilized by fluids flowing uptemperature and/or down-pressure. Flow down-temperature typically results in hydration and carbonation of rocks. Time-integrated fluid fluxes implied by visible amounts of mineral products of devolatilization reactions are on the order of 5·10²–5·10⁴ mol/cm². The model was applied to regionally metamorphosed impure carbonate rocks from south-central Maine, USA, to obtain estimates of fluid flux, flow-direction, and in-situ metamorphic-rock permeability from petrologic data. Calculated time-integrated fluxes are 10⁴–10⁶ cm³/cm² at 400°–450° C, 3,500 bars. Fluid flowed from regions of low temperature to regions of high temperature at the peak of the metamorphic event. Using Darcy's Law and estimates for the duration of metamorphism and hydrologic head, calculated fluxes are 0.1–20·10^-4 m/year and minimum permeabilities are 10^-10–10^-6 Darcy. The range of inferred permeability is in good agreement with published laboratory measurements of the permeability of metamorphic rocks.     

Contrasting mechanisms of fluid flow through adjacent stratigraphic units during regional metamorphism,south-central Maine,USA

The flow pattern of reactive metamorphic fluid through six outcrops of micaceous, carbonate-bearing sandstones from the Vassalboro Formation was determined by calculating and mapping fluid-rock ratios for numerous samples within each outcrop. The ratio of maximum to minimum measured fluid/rock varied by factors of only 1.3-22.9 in each outcrop. Fluid flow was pervasive at metamorphic grades ranging from the biotite through the sillimanite zones. Average fluid-rock ratio for the outcrops increases with increasing grade of metamorphism from 0.4 in the biotite zone to 1.4 in the sillimanite zone.The flow pattern of reactive fluid through impure sandstones of the Vassalboro Formation was different at low and medium grades from fluid flow through the limestone member of the adjacent Waterville Formation. In the biotite and garnet zones, fluid flow through the Waterville Formation was channelized with channelways corresponding to individual lithologic layers that acted as metamorphic aquifers. Fluid-rock ratios recorded by the aquifers are greater than those recorded by the intervening beds by factors of up to 50–60. At the highest grades of metamorphism (sillimanite zone), however, flow through the Waterville Formation was as pervasive as through the Vassalboro Formation.The Waterville and Vassalboro Formations experienced the same metamorphic event. The difference in pattern of fluid flow through the two formations therefore reflects the important control that lithology exerts on the permeability of rocks during metamorphism. Micaceous, carbonate-bearing sandstones evidently were more permeable than argillaceous carbonate rocks. The greater permeability of the sandstones may result from a greater concentration of grain boundaries between unlike minerals in the rocks.     

P,T, f_{{\text{CO}}_{\text{2}} } and f_{{\text{H}}_{\text{2}} {\text{O}}} during metamorphism of calcareous sediments in the Waterville-Vassalboro area,south-central Maine

In a regional metamorphic terrain where six isograds have been mapped based on mineral reactions that are observed in metacarbonate rocks, the P-T conditions and fugacities of CO₂ and H₂O during metamorphism were quantified by calculations involving actual mineral compositions and experimental data. Pressure during metamorphism was near 3,500 bars. Metamorphic temperatures ranged from 380° C (biotite-chlorite isograd) to 520° C (diopside isograd). \(f_{{\text{CO}}_{\text{2}} }\) and \(f_{{\text{CO}}_{\text{2}} }\) / \(f_{{\text{H}}_{\text{2}} {\text{O}}}\) in general is higher in metacarbonate rocks below the zoisite isograd than in those above the zoisite isograd. Calculated \(f_{{\text{CO}}_{\text{2}} }\) and \(f_{{\text{H}}_{\text{2}} {\text{O}}}\) are consistent with carbonate rocks above the zoisite isograd having equilibrated during metamorphism with a bulk supercritical fluid in which \(P_{{\text{CO}}_{\text{2}} }\) + \(P_{{\text{H}}_{\text{2}} {\text{O}}}\) = P _total. Calculations indicate that below the zoisite isograd, however, \(P_{{\text{CO}}_{\text{2}} }\) + \(P_{{\text{H}}_{\text{2}} {\text{O}}}\) was less than P_total, and that this condition is not due to the presence of significant amounts of species other than CO₂ and H₂O in the system C-O-H-S. Calculated \(P_{{\text{CO}}_{\text{2}} }\) /( \(P_{{\text{CO}}_{\text{2}} }\) + \(P_{{\text{H}}_{\text{2}} {\text{O}}}\) ) is low (0.06–0.32) above the zoisite isograd. The differences in conditions above and below the zoisite isograd may indicate that the formation of zoisite records the introduction of a bulk supercritical H₂O-rich fluid into the metacarbonates. The results of the study indicate that \(f_{{\text{CO}}_{\text{2}} }\) and \(f_{{\text{H}}_{\text{2}} {\text{O}}}\) are constant on a thin section scale, but that gradients in \(f_{{\text{CO}}_{\text{2}} }\) and \(f_{{\text{H}}_{\text{2}} {\text{O}}}\) existed during metamorphism on both outcrop and regional scales.     

Reaction mechanisms,physical conditions,and mass transfer during hydrothermal alteration of mica and feldspar in granitic rocks from south-central Maine,USA

Samples of granitic rock from south-central Maine contain primary igneous minerals altered by hydrothermal fluids. The reaction mechanisms (by which the over-all mineralogical change during the alteration was accomplished) involve several different mineral-fluid reactions at different reaction sites in the rock. The reactions involve both molecular and charged species in solution. The different reaction sites correspond to alteration of different primary igneous minerals. Biotite is partially converted to chlorite+sphene; microcline to muscovite; plagioclase to various combinations of muscovite, epidote, and calcite. The different reaction sites are linked by exchange of ions: some reaction sites produce ions consumed at other sites and vice versa. Physical conditions during the hydrothermal event are estimated from mineralogical and thermochemical data: P = 3,500 (±300) bars; T =425 ° (± 25 °)C. The fluid was characterized by X _{CO 2} = 0–0.13; ln([K⁺]/[H⁺ ]) = 10.0; ln([Ca²⁺]/[H⁺]²)=9.1; ln([Na⁺]/[H⁺]) = 10.5; Fe/(Fe+Mg) = 0.95. Amounts of secondary minerals in altered rock, when compared to the inferred mineral reactions that formed them, indicate that small but significant amounts (0.01–0.3mol/ 1,000cm³ altered rock) of CO₂, H₂O, H⁺, and K⁺ were added to the granites by fluids during the alteration, as well as lesser amounts (< 0.01–0.03 mol/1,000cm³ altered rock) of Mg²⁺, Fe²⁺, Fe³⁺, Mn²⁺, Na⁺, and Ti⁴⁺. The sole element leached from the granitic rocks during alteration was Ca in amounts 0.1–0.3 mol/1,000 cm³ rock. By estimating the composition of the hydrothermal fluids before and after reaction with the granites and by measuring the amount of material added to or subtracted from the granites during the alteration, the amount and volume of hydrothermal fluid involved can be calculated. Two independent calculations require minimum volumes in the range 100–1,000 cm³ fluid/1,000cm³ altered rock to participate in the hydrothermal event.     

The Rwenzori Mountains,a landslide-prone region?

With its exceptionally steep topography, wet climate, and active faulting, landslides can be expected to occur in the Rwenzori Mountains. Whether or not this region is prone to landsliding and more generally whether global landslide inventories and hazard assessments are accurate in data-poor regions such as the East African highlands are thus far unclear. In order to address these questions, a first landslide inventory based on archive information is built for the Rwenzori Mountains. In total, 48 landslide and flash flood events, or combinations of these, are found. They caused 56 fatalities and considerable damage to road infrastructure, buildings, and cropland, and rendered over 14,000 persons homeless. These numbers indicate that the Rwenzori Mountains are landslide-prone and that the impact of these events is significant. Although not based on field investigations but on archive data from media reports and laymen accounts, our approach provides a useful complement to global inventories overlooking this region and increases our understanding of the phenomenon in the Rwenzori Mountains. Considering the severe impacts of landslides, the population growth and related anthropogenic interventions, and the likelihood of more intense rainfall conditions, there is an urgent need to invest in research on disaster risk reduction strategies in this region and other similar highland areas of Africa.     

Interannual-decadal variability of wintertime mixed layer depths in the North Pacific detected by an ensemble of ocean syntheses

Climate Dynamics - The interannual-decadal variability of the wintertime mixed layer depths (MLDs) over the North Pacific is investigated from an empirical orthogonal function (EOF) analysis of an...