Apatites dikes

The five types of molybdenum deposits include (i) molybdenum and copper porphyry deposits (ii) Quartz vein and pipes (iii) Pegmatites and apatites dikes (iv) Contact-meta-morphic rocks and tactite bodies of silica bearing limestone and (v) Sedimentary rocks containing bedded deposits. [Pg.63]

Figure 24 Chondrite-normalized abundances of REEs in a wall-rock harzburgite from Lherz (dotted lines— whole-rock analyses), compared with numerical experiments of ID porous melt flow, after Bodinier et al. (1990). The harzburgite samples were collected at 25-65 cm from an amphibole-pyroxenite dike. In contrast with the 0-25 cm wall-rock adjacent to the dike, they are devoid of amphibole but contain minute amounts of apatite (Woodland et al., 1996). The strong REE fractionation observed in these samples is explained by chromatographic fractionation due to diffusional exchange of the elements between peridotite minerals and advective interstitial melt (Navon and Stolper, 1987 Vasseur et al, 1991). The results are shown in (a) for variable t t ratio, where t is the duration of the infiltration process and t the time it takes for the melt to percolate throughout the percolation column (Navon and Stolper, 1987). This parameter is proportional to the average melt/rock ratio in the percolation column. In (b), the results are shown for constant f/fc but variable proportion of clinopyroxene at the scale of the studied peridotite slices (<5 cm). All model parameters may be found in Bodinier et al. (1990). As discussed in the text, this model was criticized by Nielson and Wilshire (1993). An improved version taking into account the gradual solidiflcation of melt down the wall-rock thermal gradient and the isotopic variations was recently proposed by Bodinier et al. (2003).

$Figure 24 Chondrite-normalized abundances of REEs in a wall-rock harzburgite from Lherz (dotted lines— whole-rock analyses), compared with numerical experiments of ID porous melt flow, after Bodinier et al. (1990). The harzburgite samples were collected at 25-65 cm from an amphibole-pyroxenite dike. In contrast with the 0-25 cm wall-rock adjacent to the dike, they are devoid of amphibole but contain minute amounts of apatite (Woodland et al., 1996). The strong REE fractionation observed in these samples is explained by chromatographic fractionation due to diffusional exchange of the elements between peridotite minerals and advective interstitial melt (Navon and Stolper, 1987 Vasseur et al, 1991). The results are shown in (a) for variable t t ratio, where t is the duration of the infiltration process and t the time it takes for the melt to percolate throughout the percolation column (Navon and Stolper, 1987). This parameter is proportional to the average melt/rock ratio in the percolation column. In (b), the results are shown for constant f/fc but variable proportion of clinopyroxene at the scale of the studied peridotite slices (<5 cm). All model parameters may be found in Bodinier et al. (1990). As discussed in the text, this model was criticized by Nielson and Wilshire (1993). An improved version taking into account the gradual solidiflcation of melt down the wall-rock thermal gradient and the isotopic variations was recently proposed by Bodinier et al. (2003).$

The paradox of the spatial decoupling between isotopic contamination and LILE and LREE enrichment was resolved with a numerical simulation of isotopic variations during reactive porous flow (Bodinier et al., 2004). This confirmed that the isotopic contamination (e.g., " Nd/ " Nd) by the infiltrated melt is restricted to the domain between the melt source ( = dike) and the chromatographic front of the element (neodymium)—i.e., —20 cm from the dike in the studied wall rock. Numerical experiments also showed that the fractional solidification of infiltrated melt (due to amphibole cpx precipitation) accounts for the systematic increase in thorium, uranium, LREE, and P2O5, that reach a maximum in the distal apatite-bearing wall rock (>50 cm from the... [Pg.846]

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