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91.
Damien Pas Anne-Christine Da Silva Thomas Suttner Erika Kido Pierre Bultynck Monica Pondrelli Carlo Corradini David De Vleeschouwer Claudia Dojen Frédéric Boulvain 《International Journal of Earth Sciences》2014,103(2):519-538
The development and behavior of million year-scaled depositional sequences recorded within Palaeozoic carbonate platform has remained poorly examined. Therefore, the understanding of palaeoenvironmental changes that occur in geological past is still limited. We herein undertake a multi-disciplinary approach (sedimentology, conodont biostratigraphy, magnetic susceptibility (MS), and geochemistry) of a long-term succession in the Carnic Alps, which offers new insights into the peculiar evolution of one of the best example of Palaeozoic carbonate platform in Europe. The Freikofel section, located in the central part of the Carnic Alps, represents an outstanding succession in a fore-reef setting, extending from the Latest Givetian (indet. falsiovalis conodont zones) to the Early Famennian (Lower crepida conodont zone). Sedimentological analysis allowed to propose a sedimentary model dominated by distal slope and fore-reef-slope deposits. The most distal setting is characterized by an autochthonous pelagic sedimentation showing local occurrence of thin-bedded turbiditic deposits. In the fore-reef slope, in a more proximal setting, there is an accumulation of various autochthonous and allochthonous fine- to coarse-grained sediments originated from the interplay of gravity-flow currents derived from the shallow-water and deepwater area. The temporal evolution of microfacies in the Freikofel section evolves in two main steps corresponding to the Freikofel (Unit 1) and the Pal (Unit 2) limestones. Distal slope to fore-reef lithologies and associate changes are from base to top of the section: (U1) thick bedded litho- and bioclastic breccia beds with local fining upward sequence and fine-grained mudstone intercalations corresponding, in the fore-reef setting, to the dismantlement of the Eifelian–Frasnian carbonate platform during the Early to Late Frasnian time (falsiovalis to rhenana superzones) with one of the causes being the Late Givetian major rift pulse; (U2) occurrence of thin-bedded red nodular and cephalopod-bearing limestones with local lithoclastic grainstone intercalations corresponding to a significant deepening of the area and the progressive withdrawal of sedimentary influxes toward the basin, in relation with Late Frasnian sea-level rise. MS and geochemical analyses were also performed along the Freikofel section and demonstrate the inherent parallel link existing between variation in MS values and proxy for terrestrial input. Interpretation of MS in terms of palaeoenvironmental processes reflects that even though distality remains the major parameter influencing MS values, carbonate production and water agitation also play an important role. 相似文献
92.
Christophe Grenier Damien Régnier Emmanuel Mouche Hakim Benabderrahmane François Costard Philippe Davy 《Hydrogeology Journal》2013,21(1):257-270
The impact of glaciation cycles on groundwater flow was studied within the framework of nuclear waste storage in underground geological formations. The eastern section of the Paris Basin (a layered aquifer with impervious/pervious alternations) in France was considered for the last 120 ka. Cold periods corresponded with arid climates. The issue of talik development below water bodies was addressed. These unfrozen zones can maintain open pathways for aquifer recharge. Transient thermal evolution was simulated on a small-scale generic unit of the landscape including a “river” and “plain”. Coupled thermo-hydraulic modeling and simplified conductive heat transfer were considered for a broad range of scenarios. The results showed that when considering the current limited river dimensions and purely conductive heat transfer, taliks are expected to close within a few centuries. However, including coupled advection for flows from the river to the plain (probably pertinent for the eastern Paris Basin aquifer recharge zones) strongly delays talik closure (millennium scale). The impact on regional underground flows is expected to vary from a complete stop of recharge to a reduced recharge, corresponding to the talik zones. Consequences for future modeling approaches of the Paris Basin are discussed. 相似文献
93.
Laura Torres-Rondon Simon Damien Carrière Konstantinos Chalikakis Vincent Valles 《Comptes Rendus Geoscience》2013,345(5-6):241-250
Deltaic aquifers are complex due to the important heterogeneity of their structure and their hydrogeological functioning. Auger drilling provides localized, but very robust geological and hydrogeological information, while geophysical surveys can provide integrated subsurface information. An effective, easy-to-use and low-cost methodology combining geological/hydrogeological information from Auger drillings and the results from three geophysical techniques (Electromagnetic mapping, Electrical Sounding and Electrical Resistivity Tomography) is being developed to characterize the structure of a typical Mediterranean deltaic aquifer. A first hypothesis about hydrodynamic properties of the aquifer is also obtained. The study area is located in the Rhone delta (Middle Camargue/southern France). Integration of geophysical and geological techniques allowed identifying the presence and lateral extension of the Saint-Ferréol paleochannel, the vertical contact between lagoonal–fluvial deposits and the marine clayed silt that separate the superficial aquifer from the deeper aquifer. Likewise, high north–south heterogeneity and east–west homogeneity were highlighted in the study area. Presence of clay in sandy deposits in the low areas implies changes in lateral hydraulic permeability. This fact, jointed to the low hydraulic gradient, suggests a slow groundwater flow in the local system. The Rhone delta presents a typical configuration of a Mediterranean deltaic aquifer, thus this methodological approach can be used for similar deltaic Mediterranean systems. 相似文献
94.
Geordie Mark Damien R. W. Foster Peter J. Pollard Patrick J. Williams Justin Tolman Michael Darvall Kevin L. Blake 《地学学报》2004,16(2):54-61
Sodic–calcic alteration is common in mineralized hydrothermal systems, yet the relative importance of igneous vs. basinal fluid sources remains controversial. One of the most extensive volumes of sodic–calcic rocks occurs near Cloncurry, NW Queensland, and was formed by overlapping hydrothermal systems that were active synchronously with emplacement of mid‐crustal batholithic granitoids (c. 1.55–1.50 Ga). Altered rocks contain albite–oligoclase, actinolite, diopside, titanite and magnetite. Alteration was localized by: (A) composite veins and breccias containing crystallized magma intimately intergrown with hydrothermal precipitates; (B) intrusions that host setting A veins and breccias; and (C) extensive breccia and vein systems linked to regional fault systems. Isotope analyses of actinolites in settings A and B indicate calculated δ18OH2O (+8.2 to +10.6‰) and variably depleted δDH2O (?130 to ?54‰) compared with typical magmatic fluids, whereas those from setting C typically indicate calculated δ18OH2O (+8.0 to +12.8‰) and δDH2O (?29 to ?99‰). The lowest δDH2O values are interpreted as representing residual fluids after significant (> 90%) open‐system magmatic degassing. Overall the stable isotope, field, geochronological and geobarometric data suggest that these sodic–calcic alteration systems were formed by the episodic incursion of magmatic fluids that underwent minor isotopic modification as a result of varying degrees of interaction with country rocks. 相似文献
95.
The composition of carbonate minerals formed in past and present oceans is assumed to be significantly controlled by temperature and seawater composition. To determine if and how temperature is kinetically responsible for the amount of Mg incorporated in calcite, we quantified the influence of temperature and specific dissolved components on the complex mechanism of calcite precipitation in seawater. A kinetic study was carried out in artificial seawater and NaCl-CaCl2 solutions, each having a total ionic strength of 0.7 M. The constant addition technique was used to maintain [Ca2+] at 10.5 mmol kg−1 while [] was varied to isolate the role of this variable on the precipitation rate of calcite.Our results show that the overall reaction of calcite precipitation in both seawater and NaCl-CaCl2 solutions is dominated by the following reaction:
96.
Abstract— Four particles extracted from track 80 at different penetration depths have been studied by analytical transmission electron microscopy (ATEM). Regardless of their positions within the track, the samples present a comparable microstructure made of a silica rich glassy matrix embedding a large number of small Fe‐Ni‐S inclusions and vesicles. This microstructure is typical of strongly thermally modified particles that were heated and melted during the hypervelocity impact into the aerogel. X‐ray intensity maps show that the particles were made of Mg‐rich silicates (typically 200 nm in diameter) cemented by a fine‐grained matrix enriched in iron sulfide. Bulk compositions of the four particles suggest that the captured dust particle was an aggregate of grains with various iron sulfide fraction and that no extending chemical mixing in the bulb occurred during the deceleration. The bulk S/Fe ratios of the four samples are close to CI and far from the chondritic meteorites from the asteroidal belt, suggesting that the studied particles are compatible with chondritic‐porous interplanetary dust particles or with material coming from a large heliocentric distance for escaping the S depletion. 相似文献
97.
Laurent Truche Gilles Berger Damien Guillaume 《Geochimica et cosmochimica acta》2010,74(10):2894-2914
The kinetics of abiotic redox reactions induced by hydrogen are poorly documented although it represents a growing area of interest in terms of both nuclear waste storage assessment and the comprehensive study of hydrogen-rich fluid in mid-ocean ridge hydrothermal systems. We present an experimental kinetics study of pyrite reduction into pyrrhotite under significant H2 pressure and mid-hydrothermal conditions. We describe the mechanism and kinetic behavior of this reaction by combining textural and solution analyses under various conditions of temperature, pyrite particles size, H2 pressure and pH. When pH is controlled by calcite, the reaction presents all the characteristics of a coupled dissolution-precipitation mechanism occurring at the pyrite-pyrrhotite interface. By considering the chemical affinity of the coupled reaction as a function of reaction extent, we demonstrate that the spatial coupling is induced both by pyrite as a substrate for pyrrhotite nucleation and by the role of fluid chemistry at the reaction front. Far from equilibrium with respect to pyrite, the kinetics of sulfide production associated with the reaction are linearly related to the square root of time with an activation energy of 53 kJ/mol. This value is higher than what is expected for a diffusion-controlled kinetic regime. We suggest that the reaction rate is controlled both by pyrite reductive dissolution and by sulfide diffusion through the porous pyrrhotite microstructure. We provide a simple sulfide production-rate expression on the basis of our measured rate constants that can be used in geochemical modeling to further evaluate the impact of hydrogen on pyrite under nuclear waste disposal conditions. 相似文献
98.
Here we report on two separate ongoing, multi-year investigations on the dependence of the dissolution rate (R) of albite feldspar on fluid saturation state, as defined by the Gibbs free energy of reaction (ΔGr) for dissolution. The investigations are based on dissolution at pH 9.2, 150 °C and pH 3.3, 100 °C. Both studies reveal that the R–ΔGr relation is highly non-linear and sigmoidal. The kinetic data from the first study, being the most complete, can be fitted with a sigmoidal rate curve that is composed of two separate, parallel rate laws that represent distinct mechanisms of dissolution. The switch between one dominant mechanism and the other may be controlled by a critical free energy. The fact that in both studies the same type of sigmoidal R–ΔGr relation exists for dissolution at different pH and temperature condition suggests that this behavior may be universal for albite and other feldspars. Moreover, the experimental data contradict the commonly used R–ΔGr relation that is loosely based on transition state theory (TST). This has important implications with respect to the accuracy of geochemical codes that model water–rock interactions at near-equilibrium conditions. 相似文献
99.
In-Street Wind Direction Variability in the Vicinity of a Busy Intersection in Central London 总被引：3，自引：2，他引：1
Ahmed A. Balogun Alison S. Tomlin Curtis R. Wood Janet F. Barlow Stephen E. Belcher Robert J. Smalley Justin J. N. Lingard Sam J. Arnold Adrian Dobre Alan G. Robins Damien Martin Dudley E. Shallcross 《Boundary-Layer Meteorology》2010,136(3):489-513
We present results from fast-response wind measurements within and above a busy intersection between two street canyons (Marylebone Road and Gloucester Place) in Westminster, London taken as part of the DAPPLE (Dispersion of Air Pollution and Penetration into the Local Environment; www.dapple.org.uk ) 2007 field campaign. The data reported here were collected using ultrasonic anemometers on the roof-top of a building adjacent to the intersection and at two heights on a pair of lamp-posts on opposite sides of the intersection. Site characteristics, data analysis and the variation of intersection flow with the above-roof wind direction (θ ref ) are discussed. Evidence of both flow channelling and recirculation was identified within the canyon, only a few metres from the intersection for along-street and across-street roof-top winds respectively. Results also indicate that for oblique roof-top flows, the intersection flow is a complex combination of bifurcated channelled flows, recirculation and corner vortices. Asymmetries in local building geometry around the intersection and small changes in the background wind direction (changes in 15- min mean θ ref of 5°–10°) were also observed to have profound influences on the behaviour of intersection flow patterns. Consequently, short time-scale variability in the background flow direction can lead to highly scattered in-street mean flow angles masking the true multi-modal features of the flow and thus further complicating modelling challenges. 相似文献
100.
The boron isotope-pH technique is founded on a theoretical model of carbonate δ11B variation with pH that assumes that the boron isotopic composition of carbonates mirrors the boron isotopic composition of borate in solution (δ11Bcarb = δ11Bborate). Knowledge of the fractionation factor for isotope exchange between boric acid and borate in solution (α4-3), the equilibrium constant for the dissociation of boric acid (pKB*), as well as the isotopic composition of boron in seawater (δ11Bsw) are required parameters of the model.The available data suggests that both the value of α4-3 and the history of δ11Bsw are poorly constrained. However, if one assumes that δ11Bcarb = δ11Bborate, an empirical value for α4-3 can be estimated from the results of inorganic carbonate precipitation experiments. This exercise yields an α4-3 value of ∼0.974 in accordance with recent theoretical estimates, but substantially deviates from the theoretical value of 0.981 often used to estimate paleo-ocean pH. Re-evaluation of ocean pH using an α4-3 value of 0.974 and published foraminiferal δ11B values for the Cenozoic yield pH estimates that are relatively invariant, but unrealistically high (∼8.4-8.6). Uncertainty increases as foraminiferal ‘vital effects’ are considered and different models for secular changes in seawater δ11B are applied.The inability to capture realistic ocean pH possibly reflects on our understanding of the isotopic relationship between carbonate and borate, as well as the mechanism of boron incorporation in carbonates. Given the current understanding of boron systematics, pH values estimated using this technique have considerable uncertainty, particularly when reconstructions exceed the residence time of boron in the ocean. 相似文献