Daniel Hermitte

Post-collisional transition from calc-alkaline to alkaline volcanism during the Neogene in Oranie (Algeria): magmatic expression of a slab breakoff

Abstract During the Neogene, a magmatic change from calc-alkaline to alkaline types occurred in all the regions surrounding the western Mediterranean. This change has been studied in Oranie (western Algeria). In this area, potassic to shoshonitic calc-alkaline andesites (with La/Nb ratios in the range 4–6) were mainly erupted between 12 and 9 Ma. They were followed (between 10 and 7 Ma) by basalts displaying geochemical features which are transitional between calc-alkaline and alkaline lavas (La/Nb=1–1.7). After a ca. 3-Ma quiescence period, volcanic activity resumed, with the eruption of OIB-type alkaline basalts (La/Nb=0.5–0.6), from 4 to 0.8 Ma. A combined geochemical approach, using incompatible elements and Sr, Nd and O isotopes, allows us to conclude that the transitional basalts derived from the melting of a heterogeneous mantle source, at the boundary between lithosphere and asthenosphere. We propose that melting of a previously subduction-modified lithospheric mantle occurred between 12 and 10 Ma, in response to the upwelling of hot asthenosphere flowing up into an opening gap above a detached sinking slab. As a result, calc-alkaline magmas were formed. From 10 to 7 Ma, the transitional basalts were generated through melting of the boundary mantle zone between the lithosphere and the upwelling asthenosphere. During that stage, the contribution of the lithospheric source was still predominant. Then, as sinking of the oceanic slab progressed, the increasing uprise of the asthenosphere led to the formation and emplacement (from 4 to 0.8 Ma) of typical within-plate alkaline basalts derived from a plume-modified asthenospheric mantle.

Chemical fluxes during hydrothermal alteration of a 1200-m long section of dikes in the oceanic crust, DSDP/ODP Hole 504B

Abstract Chemical interactions between seawater and the oceanic crust have been widely investigated during recent years. However, most of these studies concern the uppermost volcanic part of the crust. The contribution of the underlying sheeted dike complex to the global budget of the oceans is inferred solely from some ophiolite studies and from the 500-m high-level dike section of DSDP/ODP 504B which was drilled in 1981. Hole 504B is the only place where a continuous and long (1260 m) section in the sheeted dike complex has been cored, and it is now regarded as a reference section for the upper oceanic crust. Many petrological and chemical data from these dolerites are available, including the relative proportions of veins, extensively altered adjacent rocks, and less altered “host-rocks”. For these three reasons, considering the entire dike section penetrated by Hole 504B is a unique chance to study chemical fluxes related to hydrothermal alteration of this part of the oceanic crust. The calculation of any chemical flux implies knowledge of the chemical composition of the fresh precursor (protolith). Previously, mean compositions of glasses (=P1a) or basalts from the Hole 504B volcanics have been used as protoliths. In this paper, we calculate and discuss the use of various protoliths based on dolerites from Hole 504B. We show that the most adequate and realistic protolith is the mean of individual protoliths that we calculated from the acquisition, by automatic mode, of about 1000 microprobe analyses in each thin-section of dolerite from the Hole 504B lower dikes. Consequently, PFm is further used to calculate chemical fluxes in the dike section of Hole 504B. The chemical compositions of the host-rocks adjacent to alteration halos tend to converge to that of PFm with depth, except for Fe2O3t and TiO2. Because the volume percent of alteration halos increases with depth, the total fluxes related to these halos increase with depth. This explains why the mean flux (host-rocks+halos+veins) of the upper dikes is roughly similar to the mean flux of the lower dikes. During the alteration of the entire Hole 504B dike section, the dolerites gained relatively large quantities of Fe2O3t (+4.0 g/100 cm3) and released much SiO2 (−6.8 g/100 cm3), CaO (−5.8 g/100 cm3), and TiO2 (1.6 g/100 cm3), and minor Al2O3 (−0.7 g/100 cm3) and MgO (−0.7 g/100 cm3). We show the importance of the choice of the protolith in the calculation of chemical budget, particularly for elements showing low flux values. In Hole 504B, the Mg uptake by the volcanics during low temperature alteration added to the Mg release by the dikes gives a net flux of −0.07×1014 g/year. We propose that part of the Mg uptake by the oceanic crust, which is necessary to compensate the rivers input (−1.33×1014 g/year), occurs in the underlying gabbros and/or in sections which are altered such as Trinity and Troodos ophiolites. Compared with ophiolites, fluxes calculated for elements other than Mg for the entire crust are generally similar (in tendency, if not in absolute value) to that we obtained from Hole 504B.

First paleoseismological constraints on the strongest earthquake in France (Provence) in the twentieth century

We have identified surface ruptures of M ≥ 6 earthquakes on a branch of the propagating reverse fault system that produced the strongest event recorded in France during the twentieth century (1909 Lambesc earthquake, Provence). The rate of slip on that branch is 0.05–0.3 mm/yr with a corresponding return period for M ≥ 6 events of 700–5000 yr. In addition to possibly identifying the 1909 earthquake surface rupture, by recognizing successive surface breaks of large earthquakes, this study calls for a reassessment of seismic hazard in Provence.

Slow Active Fault Detection and Imaging Using Multiple Geophysical Methods

Decreasing water table and pollution are critical problems in effective groundwater management in the Netherlands. In order to develop effective control measures to address these problems, water management scenarios need to be simulated in a groundwater model. The ice-pushed ridges of the Veluwe area are one of the main groundwater reservoirs in the Netherlands.