TY - JOUR
T1 - Reactive melt transport in the mantle and geochemical signatures of mantle-derived magmas
AU - Reiners, Peter W.
N1 - Funding Information:
I thank Bruce Nelson, Mark Ghiorso, George Bergantz, Stu McCallum, and especially Dave McTigue for helpful discussions and advice in this study. I gratefully acknowledge helpful discussions with participants of the 1996 Canary Islands Chapman Conference on Crustal Contamination in Ocean Island Magmatism, particularly Kari Cooper, Mary Reid, Mike Garcia, John Lassiter, and Dave Clague. Thanks go also to Dave Clague for allowing me to use his unpublished data from Niihau post-erosional basalts. Thorough and careful reviews by an anonymous reviewer, Erik Hauri, and especially Craig Lundstrom greatly improved this paper. This work was funded in part by NSF EAR-9628674 to Bruce Nelson, and University of Washington Geological Sciences Misch and Coombs Fellowships to Peter Reiners.
PY - 1998
Y1 - 1998
N2 - Modeling of equilibrium reactive melt transport in the mantle, including the effects of mineralogic reactions and changes in porosity in the solid matrix, provides a series of robust predictions of the consequences of reactive melt transport on magma trace element compositions. The composition of the leading melt batch through a column of reactive mantle (the melt front) will be shifted towards that of an incipient partial melt of the mantle matrix. Successive melt batches migrating through and emerging from the column will show a temporal-compositional trend reflecting exhaustion of the reactive capacity of the mantle, and will eventually return to the original input melt composition. In cases where the melt source and column matrix are similar in composition, the melt front will be enriched in incompatible elements, and the temporal-compositional trend will be one of decreasing incompatible elements in erupted melt batches with time. Cogenetic melt batches should show some type of chromatographic decoupling in trace element and/or isotopic variations. However, mineralogic reaction in the mantle column, in the form of changing matrix mode, can smooth or mask chromatographic effects on trace element abundances, though not on isotopic compositions. Thus lack of chromatographic decoupling in magma trace element abundances alone does not preclude significant melt-mantle reaction. Mineralogic reactions within the column may also impart distinctive trace element variations to melts. In particular, lherzolite-to-dunite reaction in the matrix produces large variations in heavy rare earth elements in emerging melts, whereas lherzolite-to-pyroxenite reaction produces a series of subparallel rare earth element patterns with decreasing overall abundances with time. Although these models assume end-member conditions and maximum extents of melt-mantle reaction, if reactive melt transport is an important petrogenetic process that strongly influences magma trace element compositions these chemical effects should be observed to some extent in carefully chosen sample suites. Certain magma types show chemical characteristics that are broadly similar to these predicted effects, but more complete sample suites yielding detailed temporal-compositional variations of clearly cogenetic lavas are needed to test the petrogenetic significance of reactive melt transport on erupted magmas.
AB - Modeling of equilibrium reactive melt transport in the mantle, including the effects of mineralogic reactions and changes in porosity in the solid matrix, provides a series of robust predictions of the consequences of reactive melt transport on magma trace element compositions. The composition of the leading melt batch through a column of reactive mantle (the melt front) will be shifted towards that of an incipient partial melt of the mantle matrix. Successive melt batches migrating through and emerging from the column will show a temporal-compositional trend reflecting exhaustion of the reactive capacity of the mantle, and will eventually return to the original input melt composition. In cases where the melt source and column matrix are similar in composition, the melt front will be enriched in incompatible elements, and the temporal-compositional trend will be one of decreasing incompatible elements in erupted melt batches with time. Cogenetic melt batches should show some type of chromatographic decoupling in trace element and/or isotopic variations. However, mineralogic reaction in the mantle column, in the form of changing matrix mode, can smooth or mask chromatographic effects on trace element abundances, though not on isotopic compositions. Thus lack of chromatographic decoupling in magma trace element abundances alone does not preclude significant melt-mantle reaction. Mineralogic reactions within the column may also impart distinctive trace element variations to melts. In particular, lherzolite-to-dunite reaction in the matrix produces large variations in heavy rare earth elements in emerging melts, whereas lherzolite-to-pyroxenite reaction produces a series of subparallel rare earth element patterns with decreasing overall abundances with time. Although these models assume end-member conditions and maximum extents of melt-mantle reaction, if reactive melt transport is an important petrogenetic process that strongly influences magma trace element compositions these chemical effects should be observed to some extent in carefully chosen sample suites. Certain magma types show chemical characteristics that are broadly similar to these predicted effects, but more complete sample suites yielding detailed temporal-compositional variations of clearly cogenetic lavas are needed to test the petrogenetic significance of reactive melt transport on erupted magmas.
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U2 - 10.1093/petroj/39.5.1039
DO - 10.1093/petroj/39.5.1039
M3 - Article
AN - SCOPUS:0031670356
SN - 0022-3530
VL - 39
SP - 1039
EP - 1061
JO - Journal of Petrology
JF - Journal of Petrology
IS - 5
ER -