Comparative diffusion coefficients of major and trace elements in olivine at approximately 950 degrees C from a xenocryst included in dioritic magma
Comparative diffusion coefficients of major and trace elements in olivine at approximately 950 degrees C from a xenocryst included in dioritic magma
Geology (Boulder) (April 2010) 38 (4): 331-334
- Asia
- China
- concentration
- diffusion
- diorites
- experimental studies
- Far East
- geochemistry
- hybridization
- ICP mass spectra
- igneous rocks
- ions
- laboratory studies
- laser ablation
- laser methods
- magmas
- major elements
- mass spectra
- mathematical models
- natural materials
- nesosilicates
- North China Platform
- olivine
- olivine group
- orthosilicates
- plutonic rocks
- silicates
- spectra
- theoretical models
- trace elements
- xenocrysts
The concentration profiles of 13 trace elements (Li, Na, Al, P, Ca, Sc, Ti, V, Cr, Mn, Co, Ni, and Y) were determined in a natural mantle olivine xenocryst included in a hybridized hydrous dioritic magma during cooling from approximately 1000 degrees C, which allow trace-element chemical diffusion coefficients to be evaluated relative to Mg-Fe interdiffusion under conditions that are difficult to access in the laboratory. The effective diffusion coefficients of many elements (Li, Ca, Sc, Mn, Co, Ni, and Y) fell within a factor of three of the corresponding Mg-Fe interdiffusion coefficient, in agreement with results from laboratory experiments at higher temperatures. By contrast, the concentration profiles for Na, Ti, and V implied much faster diffusion rates, while P showed no discernible diffusion. The Al and Cr profiles, which were well correlated with each other, were complex and variable on a small length scale due to local precipitation of spinel. These data show that the diffusion coefficients of cations in olivine are not simple functions of ionic charge or ionic radius, but they are likely controlled by the availability of suitable diffusion pathways.