Quick
Search: 
 
advanced search
 GSW Home    GeoRef Home    My GSW Alerts    Contact GSW    About GSW    Journals List    Help 
Reviews in Mineralogy and Geochemistry Signup for GSW Email News
JOURNAL HOME HELP CONTACT PUBLISHER SUBSCRIBE ARCHIVE SEARCH TABLE OF CONTENTS

Reviews in Mineralogy and Geochemistry; January 2008; v. 69;1; p. 363-402; DOI: 10.2138/rmg.2008.69.10
© 2008 Mineralogical Society of America
This Article
Right arrow Figures Only
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Métrich, N.
Right arrow Articles by Wallace, P. J.
Right arrow Search for Related Content
GeoRef
Right arrow GeoRef Citation

Volatile Abundances in Basaltic Magmas and Their Degassing Paths Tracked by Melt Inclusions

Nicole Métrich

Laboratoire Pierre Sue CNRS-CEA, CE-Saclay Gif sur Yvette, 91191, France, nicole.metrich@cea.fr

Paul J. Wallace

Department of Geological Sciences University of Oregon Eugene, Oregon, 97403-1272, U.S.A., pwallace@uoregon.edu

The first 20% of the full text of this article appears below.


    INTRODUCTION
 
The abundances of CO2, H2O, S and halogens dissolved in basaltic magmas are strongly variable because their solubilities and ability to be fractionated in the vapor phase depend on several parameters such as pressure, temperature, melt composition and redox state. Experimental and analytical studies show that CO2 is much less soluble in silicate melts compared to H2O (e.g., Javoy and Pineau 1991; Dixon et al. 1995). As much as 90% of the initial CO2 dissolved in basaltic melts may be already degassed at crustal depths, whereas H2O remains dissolved because of its higher solubility such that H2O contents of basaltic magmas at crustal depths may reach a few percents. Most subduction-related basaltic magmas are rich in H2O (up to 6–8 wt%; Sisson and Grove 1993; Roggensack et al. 1997; Newman et al. 2000; Pichavant et al. 2002; Grove et al. 2005) compared to mid-ocean ridge basalts (<1 wt%; Sobolev and Chaussidon 1996; Fischer and Marty 2005; Wallace 2005).

During magma movement towards the surface, exsolution of major volatile constituents (CO2, H2O) causes gas bubble nucleation, growth, and possible coalescence that exert a strong control on the dynamics of magma ascent and eruption (Anderson 1975; Sparks 1978; Tait et al. 1989). Gas bubbles have the ability to move faster than magma (Sparks 1978), particularly in low viscosity basaltic magmas. Bubble accumulation, coalescence and foam collapse give rise to differential transfer of gas slugs and periodic gas bursting (Strombolian activity; Jaupart and Vergniolle 1988, 1989) or periodic lava fountains (Vergniolle and Jaupart 1990; Philips and Wood 2001) depending on magma physical properties and ascent rate. It is also thought that strombolian and lava fountain activities . . . [Full Text of this Article]




This article has been cited by other articles:


Home page
Reviews in Mineralogy and GeochemistryHome page
K. D. Putirka
Introduction to Minerals, Inclusions and Volcanic Processes
Reviews in Mineralogy and Geochemistry, January 1, 2008; 69(1): 1 - 8.
[Full Text] [PDF]


Home page
Reviews in Mineralogy and GeochemistryHome page
J. E. Hammer
Experimental Studies of the Kinetics and Energetics of Magma Crystallization
Reviews in Mineralogy and Geochemistry, January 1, 2008; 69(1): 9 - 59.
[Full Text] [PDF]


Home page
Reviews in Mineralogy and GeochemistryHome page
T. H. Hansteen and A. Klugel
Fluid Inclusion Thermobarometry as a Tracer for Magmatic Processes
Reviews in Mineralogy and Geochemistry, January 1, 2008; 69(1): 143 - 177.
[Full Text] [PDF]


Home page
Reviews in Mineralogy and GeochemistryHome page
J. Blundy and K. Cashman
Petrologic Reconstruction of Magmatic System Variables and Processes
Reviews in Mineralogy and Geochemistry, January 1, 2008; 69(1): 179 - 239.
[Full Text] [PDF]


Home page
Reviews in Mineralogy and GeochemistryHome page
A. J.R. Kent
Melt Inclusions in Basaltic and Related Volcanic Rocks
Reviews in Mineralogy and Geochemistry, January 1, 2008; 69(1): 273 - 331.
[Full Text] [PDF]


Home page
Reviews in Mineralogy and GeochemistryHome page
G. Moore
Interpreting H2O and CO2 Contents in Melt Inclusions: Constraints from Solubility Experiments and Modeling
Reviews in Mineralogy and Geochemistry, January 1, 2008; 69(1): 333 - 362.
[Full Text] [PDF]




JOURNAL HOME HELP CONTACT PUBLISHER SUBSCRIBE ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2009 by Mineralogical Society of America