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141.
The purpose of this research is to improve the retrieval accuracy for the suspended sediment concentration(SSC) from in situ and satellite remote sensing measurements in turbid East China estuarine and coastal waters. For this aim, three important tasks are formulated and solved: 1) an estimation of remote-sensing reflectance spectra R_(rs)(λ) after atmospheric correction; 2) an estimation of R_(rs)(λ) from the radiometric signals above the air-water surface; and 3) an estimation of SSC from R_(rs)(λ). Six different models for radiometric R_(rs)(λ) determination and 28 models for SSC versus R_(rs)(λ) are analyzed based on the field observations made in the Changjiang River estuary and its adjacent coastal area. The SSC images based on the above-mentioned analysis are generated for the area. 相似文献
142.
‘Invisible gold’ in bismuth chalcogenides 总被引:1,自引:0,他引:1
Cristiana L. Ciobanu Nigel J. Cook Joël Brugger Leonid V. Danyushevsky 《Geochimica et cosmochimica acta》2009,73(7):1970-1999
Gold concentrations have been determined by LA-ICPMS in bismuth chalcogenides (tellurides and sulfosalts, minerals with modular structures; chalcogen X = Te, Se, and S) from 27 occurrences. Deposit types include epithermal, skarn, intrusion-related and orogenic gold. The samples comprised minerals of the tetradymite group, aleksite series, bismuth sulfosalts (cosalite, lillianite, hodrushite, bismuthinite, and aikinite), and accompanying altaite. Gold concentrations in phases of the tetradymite group range from <0.1 to 2527 ppm. Phases in which Bi > X tend to contain lower gold concentrations than Bi2X3 minerals (tellurobismuthite and tetradymite). Cosalite and lillianite contain Au concentrations ranging up to 574 and 3115 ppm, respectively. Bismuthinite derivatives have lower Au concentrations: <2 ppm in bismuthinite and up to 542 ppm in aikinite. In our samples, Au concentrations in altaite range from <0.2 to 1662 ppm.Smoother parts of the LA-ICPMS profiles suggest lattice-bound gold, whereas irregularities on the profiles are best explained by the presence of gold particles (?1 μm in diameter). Plotting Au vs. Ag for the entire dataset gives a wedge-shaped distribution, suggesting that Ag underpins Au uptake in both bismuth tellurides and sulfosalts. In the tellurides, correlation trends suggest statistical substitution of Ag(Au), together with Pb, into the octahedral site in the layers. In sulfosalts, Au follows coupled substitutions in which M1+ (Ag, Cu) enters the structure. In tellurides, the presence of van der Waals gaps at chalcogen-chalcogen contacts provides for p-type semi-conductive properties critical for gold scavenging from fluids. Such weak bonds may also act as sites for nucleation of Au (nano)particles. In sulfosalts, contacts between different species that replace one another are also highly predictable to act as traps for (nano)particulate gold.Invisible gold in Bi-chalcogenides is useful to (i) identify trends of orefield zonation, (ii) discriminate between ‘melt’ and ‘fluid-driven’ scavenging, and (iii) interpret replacement and remobilisation processes. Bismuth chalcogenides have the potential to be significant Au carriers in sulfide-poor Au systems, e.g., intrusion-related gold, with impact on the overall Au budget if mean Au concentrations are high enough and the minerals are sufficiently abundant. 相似文献
143.
Yuenyong Panjasawatwong Leonid V. Danyushevsky Anthony J. Crawford Keith L. Harris 《Contributions to Mineralogy and Petrology》1995,118(4):420-432
An experimental investigation of plagioclase crystallization in broadly basaltic/andesitic melts of variable Ca# (Ca/(Ca+Na)*100)
and Al# (Al/(Al+Si)*100) values and H2O contents has been carried out at high pressures (5 and 10 kbar) in a solid media piston-cylinder apparatus. The H2O contents of glasses coexisting with liquidus or near-liquidus plagioclases in each experiment were determined via an FTIR
spectroscopic technique. This study has shown that melt Ca# and Al#, H2O content and crystallization pressure all control the composition of liquidus plagioclase. Increasing melt Ca# and Al# increase
An content of plagioclase, whereas the effect of increasing pressure is the opposite. However, the importance of the role
played by each of these factors during crystallization of natural magmas varies. Melt Ca# has the strongest control on plagioclase
An content, but melt Al# also exerts a significant control. H2O content can notably increase the An content of plagioclase, up to 10 mol % for H2O-undersaturated melts, and 20 mol % for H2O-saturated melts. Exceptionally calcic plagioclases (up to An100) in some primitive subduction-related boninitic and related rocks cannot be attributed to the presence of the demonstrated
amounts of H2O (up to 3 wt %). Rather, they must be due to the involvement of extremely refractory (CaO/Na2O>18) magmas in the petrogenesis of these rocks. Despite the refractory nature of some primitive MORB glasses, none are in
equilibrium with the most calcic plagioclase (An94) found in MORB. These plagioclases were likely produced from more refractory melts with CaO/Na2O = 12–15, or from melts with exceptionally high Al2O3(>18%). Magmas of appropriate compositions to crystallize these most calcic plagioclases are sometimes found as melt inclusions
in near liquidus phenocrysts from these rocks, but are not known among wholerock or glass compositions. The fact that such
melts are not erupted as discrete magma batches indicates that they are effectively mixed and homogenized with volumetrically
dominant, less refractory magmas. The high H2O contents (∼ 6 wt%) in some high-Al basaltic arc magmas may be responsible for the existence of plagioclases up to An95 in arc lavas. However, an alternative possibility is that petrogenesis involving melts with abnormally high CaO/Na2O values (> 8) may account for the presence of highly anorthitic plagioclases in these rocks.
Received: 31 August 1993 / Accepted: 20 May 1994 相似文献