Skip Navigation

This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (PDF) Freely available
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (13)
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by ASHWORTH, J. R.
Right arrow Articles by CHAMBERS, A. D.
Right arrow Search for Related Content
GeoRef
Right arrow GeoRef Citation
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Journal of Petrology Volume 41 Number 2 Pages 285-304 2000
© Oxford University Press 2000

Symplectic Reaction in Olivine and the Controls of Intergrowth Spacing in Symplectites

J. R. ASHWORTH,* and A. D. CHAMBERS

SCHOOL OF EARTH SCIENCES, UNIVERSITY OF BIRMINGHAM, EDGBASTON, BIRMINGHAM B15 2TT, UK

Symplectite growth is analysed in terms of non-equilibrium thermodynamics and maximum rate of energy dissipation. For a given reaction, the spacing {lambda} of lamellae or rods is predicted to be proportional to the cube root of L{delta}/v, where v is reaction rate and L is the Onsager diffusion coefficient of a reference element in the reaction front of width {delta}. The result is comparable with, but not identical to, metallurgical theory for discontinuous precipitation in alloys. It is reasoned that concentration-gradient constraints place a lower limit on {lambda}, which depends on grain-boundary energy {gamma}. An upper limit {gamma} ~ 0·3 J/m2 is thus estimated using literature data from experimental oxidation of olivine. Combined with new observations on exsolution symplectites in olivine from the Lilloise intrusion, Greenland, this suggests that the exsolution reaction took place above 800°C. Using previous modelling of a corona with a symplectic layer, {gamma} ~ 1 J/m2 is estimated for hornblende–spinel symplectite. The energy driving diffusion plus grain-boundary production in the reaction front was a small proportion of the overall affinity of the corona reaction. The theory explains symplectite growth over a wide range of igneous and metamorphic temperatures and timescales.

KEY WORDS: discontinuous precipitation; energy dissipation; grain-boundary energy; olivine; symplectite


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
J PetrologyHome page
L. A. Coogan, G. R. T. Jenkin, and R. N. Wilson
Contrasting Cooling Rates in the Lower Oceanic Crust at Fast- and Slow-spreading Ridges Revealed by Geospeedometry
J. Petrology, November 1, 2007; 48(11): 2211 - 2231.
[Abstract] [Full Text] [PDF]


Home page
American MineralogistHome page
T. N. Yang, T. N. Yang, Z. Q. Xu, and M. Leech
Mass balance during retrogression of eclogite-facies minerals in the Rongcheng eclogite, eastern Sulu ultrahigh-pressure terrane, China
American Mineralogist, October 1, 2004; 89(10): 1525 - 1532.
[Abstract] [Full Text] [PDF]


Home page
American MineralogistHome page
W. D. Carlson
Scales of disequilibrium and rates of equilibration during metamorphism
American Mineralogist, February 1, 2002; 87(2-3): 185 - 204.
[Abstract] [Full Text] [PDF]


Home page
American MineralogistHome page
G. Markl, M. Marks, and R. Wirth
The influence of T, aSiO2, and fO2 on exsolution textures in Fe-Mg olivine: An example from augite syenites of the Ilimaussaq Intrusion, South Greenland
American Mineralogist, January 1, 2001; 86(1-2): 36 - 46.
[Abstract] [Full Text] [PDF]



Disclaimer:
Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.