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671.
Bernard Charlier Olivier Namur Simon Malpas Cédric de Marneffe Jean-Clair Duchesne Jacqueline Vander Auwera Olivier Bolle 《Lithos》2010,117(1-4):119-134
The late-Proterozoic Allard Lake ilmenite deposit is located in the Havre-Saint-Pierre anorthosite complex, part of the allochtonous polycyclic belt of the Grenville Province. Presently the world's largest Fe–Ti oxide deposit, it had a pre-mining amount in excess of 200 Mt at grades over 60 wt.% hemo-ilmenite. The main ore body is a funnel-shaped intrusion, measuring 1.03 × 1.10 km and 100–300 m-thick. Two smaller bodies are separated by faults and anorthosite. The ore is an ilmenite-rich norite (or ilmenitite) made up of hemo-ilmenite (Hem22.6–29.4, 66.2 wt.% on average), andesine plagioclase (An45–50), aluminous spinel and locally orthopyroxene. Whole-rock chemical compositions are controlled by the proportions of ilmenite and plagioclase ± orthopyroxene which supports the cumulate origin of the deposit. Ore-forming processes are further constrained by normal and reverse fractionation trends of Cr concentration in cumulus ilmenite that reveal multiple magma emplacements and alternating periods of fractional crystallization and magma mixing. Mixing of magmas produced hybrids located in the stability field of ilmenite resulted in periodic crystallization of ilmenite alone. The unsystematic differentiation trends in the Allard Lake deposit, arising from a succession of magma pulses, hybridisation, and the fractionation of hemo-ilmenite alone or together with plagioclase suggest that the deposit formed within a magma conduit. This dynamic emplacement mechanism associated with continuous gravity driven accumulation of Fe–Ti oxides and possibly plagioclase buoyancy in a fractionating ferrobasalt explains the huge concentration of hemo-ilmenite. The occurrence of sapphirine associated with aluminous spinel and high-alumina orthopyroxene (7.6–9.1 wt.% Al2O3) lacking exsolved plagioclase supports the involvement of a metamorphic overprint during the synchronous Ottawan orogeny, which is also responsible for strong textural equilibration and external granule of exsolved aluminous spinel due to slow cooling. 相似文献
672.
Structures affected by mining subsidence are exposed to heavy damage potential in relation to the induced tensile or compressive horizontal ground strains. This study intends to specify and compare the mining subsidence effect in terms of building transmitted movements or induced stresses, given the soil–structure interaction phenomena produced at the interface between a “stiff” elastic structure and a “flexible” elastoplastic soil. 相似文献
673.
Dehydration of dioctahedral aluminous phyllosilicates: thermodynamic modelling and implications for thermobarometric estimates 总被引:1,自引:1,他引:0
Benoît Dubacq Olivier Vidal Vincent De Andrade 《Contributions to Mineralogy and Petrology》2010,159(2):159-174
We propose a solid-solution model for dioctahedral aluminous phyllosilicates accounting for the main compositional variations,
including hydration, observed in natural smectites, interlayered illite/smectite, illites, and phengites from diagenetic to
high-grade metamorphic conditions. The suggested formalism involves dehydrated micas and hydrated pyrophyllite-like thermodynamic
end-members. With these end-members, the equilibrium conditions of quartz + water + K-bearing mica-like phyllosilicates of
fixed 2:1 composition are represented by a line in P–T space along which the interlayer water content varies. The relevant thermodynamic properties required for the calculation
of equilibrium conditions were derived using a set of 250 natural data of known maximal temperature and pressure conditions,
which covers a range between 25°C and few MPa to 800°C and 5 GPa. The temperatures calculated at fixed pressure with our model
are in fair agreement with those reported in the literature for the 250 natural data. At low temperature and pressure, the
amount of interlayer water in K-deficient phengite and illite is predicted to reach 100% of the apparent vacancies, which
is consistent with previous values reported in the literature. Although the amount of interlayer water is predicted to decrease
with pressure and temperature, it is calculated to be significant in K-deficient phengite from LT–HP pelites metamorphosed
at about 350°C, 10 kbar. The presence of molecular water in the interlayer site of such phengites has been confirmed by FTIR
mapping. Its implications for P–T estimates are discussed. 相似文献
674.
Hydraulic conductivity distribution in crystalline rocks, derived from inflows to tunnels and galleries in the Central Alps, Switzerland 总被引:4,自引:3,他引:1
Inflow data from 23 tunnels and galleries, 136 km in length and located in the Aar and Gotthard massifs of the Swiss Alps, have been analyzed with the objective (1) to understand the 3-dimensional spatial distribution of groundwater flow in crystalline basement rocks, (2) to assess the dependency of tunnel inflow rate on depth, tectonic overprint, and lithology, and (3) to derive the distribution of fracture transmissivity and effective hydraulic conductivity at the 100-m scale. Brittle tectonic overprint is shown to be the principal parameter regulating inflow rate and dominates over depth and lithology. The highest early time inflow rate is 1,300 l/s and has been reported from a shallow hydropower gallery intersecting a 200-m wide cataclastic fault zone. The derived lognormal transmissivity distribution is based on 1,361 tunnel intervals with a length of 100 m. Such interval transmissivities range between 10?9 and 10?1 m2/s within the first 200–400 m of depth and between 10?9 and 10?4 m2/s in the depth interval of 400–1,500 m below ground surface. Outside brittle fault zones, a trend of decreasing transmissivity/hydraulic conductivity with increasing depth is observed for some schistous and gneissic geological units, whereas no trend is identified for the granitic units. 相似文献
675.
Nicolas Estrade Jean Carignan Jeroen E. Sonke Olivier F.X. Donard 《Geostandards and Geoanalytical Research》2010,34(1):79-93
With the emergence of new analytical techniques and the expansion of scientific fields explored by using mercury isotopes, the community needs reference materials (RM) to validate and assure the accuracy of the results. The present work investigates (1) the characterisation of secondary RM in order to validate analytical systems, (2) the effects of two complex matrices on isotopic determination using stannous chloride cold vapour generation coupled to MC-ICP-MS (CV-MC-ICP-MS), (3) the effects of multiple digestion techniques for total Hg extraction and (4) the characterisation of nine geo-bio-environmental RM. Two secondary mono-elemental RMs analysed using two different analytical setups yielded isotopic compositions on δ202Hg of −3.54 ± 0.27‰ (CRPG-F65A, 2SD, n = 38) and +2.59 ± 0.19‰ (CRPG-RL24H, 2SD, n = 30) relative to the CRM NIST SRM 3133. These two RMs cover the whole range of Hg isotopic fractionation in natural samples and are made available to the scientific community. Complex fly ash and hydroxysulfate green rust matrices were synthesised, spiked with NIST SRM 3133, then digested and finally analysed versus the mono-elemental NIST SRM 3133 to show potential effect of these complex matrices during CV-MC-ICP-MS. Three digestions techniques, including traditional acid digestion, microwave digestion and high pressure-high temperature digestion, were applied to the lichen RM BCR-482 in order to compare advantages and drawbacks of these methods. Finally, the isotopic compositions of nine RMs including soils (NIST SRM 2711; GXR-2; GSS-4), sediment (GSD-10), jasperoid (GXR-1), ore deposit (GXR-3), fly ashes (BCR-176; BCR-176R) and lichen (BCR-482) are reported. These selected materials have δ202Hg values ranging from −1.75‰ to +0.11‰. Some RMs also presented mass-independent fractionation with Δ199Hg and Δ201Hg of up to −0.6‰. 相似文献
676.
In this paper, we applied a reliable technique for measuring Fe isotope variations in coastal seawater at nanomolar levels. Iron was directly pre-concentrated from acidified seawater samples onto a nitrilotriacetic acid chelating resin and further purified using anion-exchange resin. Sample recovery, determined using a standard addition method, was essentially quantitative. Iron was then determined using a high-resolution multicollector ICP-MS (Neptune) coupled to an ApexQ desolvation introduction system. The external precision for δ56Fe values was 0.11‰ (2s) when using total a Fe quantity between 25 and 100 ng. We initially applied this technique to measure the Fe isotope composition of dissolved Fe from several coastal environments in the north-eastern United States and we observed a range of δ56Fe values between -0.9‰ and 0.1‰ relative to the IRMM-14 reference material. Iron isotope compositions of several reference water materials for inter-laboratory comparisons were also reported. Our results suggest that iron in coastal seawater, derived from benthic diagenesis and/or groundwater has negative Fe isotopic signatures that are distinct from other iron sources such as atmospheric deposition and rivers. 相似文献
677.
Djim M. L. Diongue Christine Stumpp Olivier Roupsard Didier Orange Frederic C. Do Serigne Faye 《水文研究》2023,37(1):e14787
Sustainable water management in semi-arid agriculture practices requires quantitative knowledge of water fluxes within the soil-vegetation-atmosphere system. Therefore, we used stable-isotope approaches to evaluate evaporation (Ea), transpiration (Ta), and groundwater recharge (R) at sites in Senegal's Groundnut basin and Ferlo Valley pasture region during the pre-monsoon, monsoon, and post-monsoon seasons of 2021. The approaches were based upon (i) the isothermal evaporation model (for quantifying Ea); (ii) water and isotope mass balances (to partition Ea and Ta for groundnut and pasture); and (iii) the piston displacement method (for estimating R). Ea losses derived from the isothermal evaporation model corresponded primarily to Stage II evaporation, and ranged from 0.02 to 0.09 mm d−1 in the Groundnut basin, versus 0.02–0.11 mm d−1 in Ferlo. At the groundnut site, Ea rates ranged from 0.01 to 0.69 mm d−1; Ta was in the range 0.55–2.29 mm d−1; and the Ta/ETa ratio was 74%–90%. At the pasture site, the ranges were 0.02–0.39 mm d−1 for Ea; 0.9–1.69 mm d−1 for Ta; and 62–90% for Ta/ETa. The ETa value derived for the groundnut site via the isotope approach was similar to those from eddy covariance measurements, and also to the results from the previous validated HYDRUS-1D model. However, the HYDRUS-1D model gave a lower Ta/ETa ratio (23.2%). The computed groundwater recharge for the groundnut site amounted to less than 2% of the local annual precipitation. Recommendations are made regarding protocols for preventing changes to isotopic compositions of water in samples that are collected in remote arid regions, but must be analysed days later. The article ends with suggestions for studies to follow up on evidence that local aquifers are being recharged via preferential pathways. 相似文献