Accumulation of organic and inorganic carbon in Pliocene–Pleistocene sediments along the SW African margin

The Ocean Drilling Program Leg 175 recovered a unique series of stratigraphically continuous sedimentary sections along the SW African margin, an area which is presently affected by active coastal upwelling. The accumulation rates of organic and inorganic carbon are a major component of this record. Four Leg 175 sites (1082, 1084, 1085, 1087) are chosen as part of a latitudinal transect from the present northern to southern boundaries of the Benguela Current upwelling system, to decipher the Pliocene–Pleistocene history of biogenic production and its relationship with global and local changes in oceanic circulation and climate. The pattern of CaCO₃ and C_org mass accumulation rates (MARs) over 0.25-Myr intervals indicates that the evolution of carbon burial is highly variable between the northern and the southern Benguela regions, as well as between sites that have similar hydrological conditions. This, as well as the presence over most locations of high-amplitude, rapid changes of carbon burial, reflect the partitioning of biogenic production and patterns of sedimentation into local compartments over the Benguela margin. The combined mapping of CaCO₃ and C_org MARs at the study locations suggests four distinct evolutionary periods, which are essentially linked with major steps in global climate change: the early Pliocene, the mid-Pliocene warm event, a late Pliocene intensification of northern hemisphere glaciation and the Pleistocene. The early Pliocene spatially heterogeneous patterns of carbon burial are thought to reflect the occurrence of mass-gravitational movements over the Benguela slope which resulted in disruption of the recorded biogenic production. This was followed (3.5–3 Ma) by an episode of peak carbonate accumulation over the whole margin and, subsequently, by the onset of Benguela provincialism into a northern and a southern sedimentary regime near 2 Ma. This mid and late Pliocene evolution is interpreted as a direct response to changes in the ventilation of bottom and intermediate waters, as well as to dynamics of the subtropical gyral circulation and associated wind stress.     

Diel variation of benthic respiration in a coral reef sediment (Reunion Island,Indian Ocean)

Oxygen and total dissolved inorganic carbon (DIC) fluxes at the water–sediment interface were measured using benthic chambers to assess the short-term variations of community respiration (CR) in the back reef sediments of Reunion Island (Indian Ocean). Benthic CR had a daily cycle of minimal (6:00 AM) and maximal values (6:00 PM), showing increases of oxygen and DIC fluxes of 2.8- and 3.8-fold, respectively. Average CR values were observed at midday and midnight. The evolution of fluxes was positively related to oxygen concentration in ambient water, but not to temperature changes. In the study area, high daytime primary production augments the amount of energy available for community metabolism and increases benthic respiration. The benthic communities are therefore subjected to short-term variable environmental conditions with oxygen supersaturation during the day, and moderately hypoxic conditions at the end of the night.     

Petroleum accumulation and leakage in a deeply buried carbonate reservoir,Níspero field (Mexico)

The filling history of the Níspero deeply buried Lower Cretaceous carbonate reservoir (below 4000 m) from the south part of Gulf of Mexico was studied using a combination of data from petrography, stable isotopes and fluid inclusions and compared with a one-dimensional burial model to derive timing.     

Gravimetry on the Erimo Seamount, Japan

A gravimetric survey on the sea-bottom was performed on the Erimo Seamount by the French submersible “Nautile”. It took place during the second phase of the Kaiko French-Japanese Program. The reference station was established on the Erimo submarine observatory at a depth of 3942 m and from this point the survey of four stations was carried out. The obtained accuracy of the gravity field measurements was about 0.1 mGal.

A three-dimensional model of the seamount and its surroundings was constrained by the free-air anomaly values from the sea surface and from the sea bottom and by the perfect Seabeam topography survey of the whole area. The model which fitted the observed values best, allowed us to identify a low-density layer of coral limestones and volcaniclastics capping the seamount and to define the geometry of the interface between basalts and coral rocks.     

Multisite surface reaction versus transport control during the hydrolysis of a complex oxide

Dissolution experiments of a tholeiite basalt glass carried out at different pH and T (up to 300°C) using a rotatingdisc apparatus show that, depending on pH and T, dissolution can be controlled by one of the following steps: (1) surface reaction; (2) transport of reactants in solution; and (3) mixed reaction. The activation energies of these different processes were found to be 60, 9 and 15–50 kJ mol⁻¹, respectively. Taking account of these results, it appears likely that surface reactions are not rate limiting for the hydrolysis of most crystalline silicate minerals in hydrothermal and metamorphic processes, and that caution should be exercised when predicting rate of reactions at high temperatures solely on the basis of activation energies measured at low temperatures.

Comparison of experimental and theoretical potentiometric titrations of the basalt glass and its constituent oxides indicates that the adsorption of H⁺ and OH⁻ ions at the basalt surface is metal cation specific and that the net adsorption can be predicted from the sole knowledge of the acidity constants of the network-forming constituent oxides. We found that in the acidic pH region dissolution is promoted by the adsorption of H⁺ on al and Fe surface sites while in the basic region, dissolution is promoted by the adsorption of OH⁻ on Si sites. The combination of the two distinct types of surface sites, Al and Fe on the one hand, and Si on the other hand, results in a dissolution rate minimum at a pH-value between the pH_zpc of the two groups of oxide components. Linear regressions with a slope n=3.8 are observed both in acid and alkaline solutions in logarithmic plots of the rate of dissolution vs. the surface charge. The value of n, which represents the number of protonation or hydroxylation steps prior to metal detachment, has been found equal to the mean valence of the network-forming metals.

Combining concepts of surface coordination chemistry with transition state theory afforded characterisation of the activated complexes involved in basalt dissolution processes. From the values obtained for the thermodynamic properties of activation for basalt dissolution it is assumed that the activated complexes formed during the H₂O-promoted dissolution of the basalt glass are more tightly bonded than those formed during H⁺- or OH⁻-promoted dissolution.     

Effet de la teneur en eau d'un sol sur la réduction bactérienne d'oxydes de fer

Iron-reducing activity of autochthonous bacteria from two temporary hydromorphic soils is evaluated by the study of iron reductive dissolution, as a function of water content. The release of ferrous iron in solution is coupled to the mineralization of soil organic carbon. Water soil saturation is not necessary for iron reductive dissolution, since the highest dissolution is obtained for a wet, but not water-saturated soil (100% of water holding capacity WHC), and dissolution is also very high in a soil at 75% WHC. To cite this article: S.J. Stemmler et al., C. R. Geoscience 336 (2004).     

Seismic scattering and shallow structure of the moon in oceanus procellarum

Long, reverberating trains of seismic waves produced by impacts and moonquakes may be interpreted in terms of scattering in a surface layer overlying a non-scattering elastic medium. Model seismic experiments are used to qualitatively demonstrate the correctness of the interpretation. Three types of seismograms are found, near impact, far impact and moonquake. Only near impact and moonquake seismograms contain independent information. Details are given in the paper of the modelling of the scattering processes by the theory of diffusion.Interpretation of moonquake and artificial impact seismograms in two frequency bands from the Apollo 12 site indicates that the scattering layer is 25 km thick, with a Q of 5000. The mean distance between scatterers is approximately 5 km at 25 km depth and approximately 2 km at 14 km depth; the density of scatterers appears to be high near the surface, decreasing with depth. This may indicate that the scatterers are associated with cratering, or are cracks that anneal with depth. Most of the scattered energy is in the form of scattered surface waves.Communication presented at the Lunar Science Institute Conference on Geophysical and Geochemical Exploration of the Moon and Planets, January 10–12, 1973.     

Evidence of a Mixed-Layer Dynamics Contribution to the Entrainment Process

The internal thermal boundary layer developing over the Mediterranean during a cold-air outbreak associated with a Tramontane event has been studied by means of airborne lidar, in situ sensors, and a modelling approach that consisted of nesting the University of Washington (UW) planetary boundary-layer (PBL) model in an advective zero-order jump model. This approach bypasses some of the deficiencies associated with each model: the absence of the dynamics in the mixed layer for the zero-order jump model and the lack of an inversion at the PBL top for the UW PBL model. Particular attention is given to the parameterization of the entrainment flux at the PBL top. Values of the entrainment closure parameter derived with the model when matching PBL structure observations are much lower than those derived with standard zero-order jump models. They also are in good agreement with values measured in different meteorological situations by other studies. This improvement is a result of the introduction of turbulent kinetic energy production in the mixed layer.     

Etude des solutions solides des néphélines (Na,K)AlSiO4 et (Na,Rb)AlSiO4

Ion exchange equilibrium of nepheline solid solutions (Na, K)AlSiO₄ and (Na, Rb)AlSiO₄ with hydrothermal solutions has been studied at 600°C and 2000 bars. The behaviour of dilute solid solutions was specially investigated.Na-Rb ion exchange data can be represented satisfactorily by a model taking into account the existence of two different sites in the structure of nepheline. At 600°C Rb atoms substitute almost exclusively for Na atoms situated in the larger sites. On the other hand, this model only partially applies to Na-K ion exchange equilibrium.Finally, the importance of the ion exchange data concerning extremely dilute solutions to calculate activity-composition diagrams is emphasized with special reference to the nepheline solid solutions.     

Equilibrium state of diopside-bearing harzburgites from ophiolites: Geobarometric and geodynamic implications

The bulk compositions of coexisting enstatite and diopside in basal lherzolites and clinopyroxene-bearing harzburgites from ophiolitic complexes are typical of solidus/subsolidus equilibria, but for a few texturally distinct magmatic diopsides. They would presumably reflect the state of equilibrium at the time they last coexisted with liquid as the rocks reentered subsolidus conditions. The total lack of correlation between Al and Ca concentrations shows that the compositional scatter observed for any given massif, results from analytical errors related to extensive exsolution and serpentinization, rather than from differences in equilibrium conditions. However, significant differences are found between the residual ophiolitic lherzolites from Hare Bay, Newfoundland, and from Xigaze, Tibet, two massifs selected for their distinct structural and textural features. As for thermobarometry techniques relevant to these rocks, the best barometer found is an empirical relation for the expression of pressure as a virtually temperature-independent function of the ratioK _f=(X _Di ^opx )/(1 –X _Di ^cpx ), in agreement with semi-quantitative models based on natural solid solutions. Temperatures are then simply derived from a surface-fitting expression relating pressure, temperature and diopside-solvus compositions, according to a regularX _En ^cpx solution model (CMS) corrected for the effect of Al in the spinel facies. Application of these techniques yield pressures of 0.4 and 1.4 GPa, i.e. depths from sea-bottom of about 13 and 43 km, for temperatures of 1,170 and 1,300° C for the ophiolitic lherzolites of Tibet and New-foundland, respectively, in good agreement with dry-solidus data by radioactive tracing and with geothermal-model estimates for ridges.