Abstract
Mineral buffers control the composition of most volatile components of magmas and dissolved species in geothermal fluids. The only element which occurs in significant quantities in volcanic and geothermal fluids and is not controlled by mineral buffers is chlorine. It is argued that in absence of marine influence, geothermal fluids reflect the chlorine content of associated magmatic fluids. The chlorine content of oceanic volcanic rocks has a positive correlation with elements, which are believed to indicate a heterogenous source region. Since the source is generally believed to be the Earth's mantle, the implication is that the mantle is heterogenous with regard to chlorine and other volatiles. Such heterogeneities would have important consequences for genesis and distribution of ore. All major magma types of the oceanic environment occur in Iceland. Their spatial distribution is closely related to a volcanotectonic pattern, suggesting crustal control. A geophysical model of crustal accretion in a rift zone is used in conjunction with classical petrology to predict geochemical processes in a rift zone crust. The model has two kinematic parameters—drift rate and subsidence rate—which combined describe trajectories of mass particles deposited on the surface. When considering in conjunction with thermal gradients of the rift zone a series of metamorphic reactions and chemical fractionation processes are bound to occur, eventually resulting in a layering of the oceanic crust. The physical parameters result in a derived variable, rift zone residence time, which depends on the width of a rift zone. Long residence times in a wide rift zone lead to multistage recycling of material. Other properties of the model, based on geometric arrangement of productive fissure swarms within a rift zone, explain off-rift volcanism as directly related to rift zone processes, either as plate trapped magmatic domains or a transgressive thermal anomaly into an older crust. Off-rift volcanism is accordingly not fed directly by mantle derived liquids. The model predicts that all volcanic fluids, with the exception of those which are associated with the most primitive olivine tholeiites, are partly or wholly recycled through all stages of hydrothermal and metamorphic reactions. In that sense associated volcanic and geothermal systems are a part of the same chemical fractionation column. It is concluded that the chemistry of fluids in volcanic and geothermal systems can be viewed in the perspective of predictable crustal fractionation processes before any conclusion need be drawn concerning more deep seated causes for chemical anomalies.
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