PETROLOGY AND GEOCHEMISTRY OF BONINITES FROM THE NORTH TERMINATION OF THE TONGA TRENCH - CONSTRAINTS ON THE GENERATION CONDITIONS OF PRIMARY HIGH-CA BONINITE MAGMAS

被引:349
作者
SOBOLEV, AV
DANYUSHEVSKY, LV
机构
[1] RUSSIAN ACAD SCI, VERNADSKY INST GEOCHEM & ANALYT CHEM, MOSCOW 117975, RUSSIA
[2] UNIV TASMANIA, DEPT GEOL, HOBART, TAS 7001, AUSTRALIA
基金
俄罗斯基础研究基金会;
关键词
D O I
10.1093/petrology/35.5.1183
中图分类号
P3 [地球物理学]; P59 [地球化学];
学科分类号
0708 ; 070902 ;
摘要
We report here a detailed mineralogical, geochemical, and experimental study of a high-Ca boninite suite from the northern termination of the Tonga trench. Most samples are strongly olivine porphyritic and show a significant range of phenocryst compositions including a very refractory olivine-spinel assemblage Fo(94)-Cr-N=87. They are also characterized by a wide range of incompatible-element contents, e.g., (La/Yb)(N) varies from 0.5 to 16, whereas compatible major-element concentrations (Al2O3, FeO, CaO, SiO2, and MgO) remain essentially the same. Primary melt compositions for the suite were established on the basis of an experimental study of melt inclusions in phenocrysts and numerical modelling of the reverse of fractional crystallization. Tongan primary melts are characterized by high MgO contents (22-24 wt.%) and originated in the mantle wedge at pressures of 20-25 kbar and temperatures of 1450-1550 degrees C. H2O contents in primary melts were estimated from direct measurements of melt inclusions by ion probe, and range from 2.0 to 1.0 wt.%, and a strong correlation exists between H2O and other incompatible element contents. The primary melts crystallized in the presence of an H2O-rich fluid in the temperature range 1390-1150 degrees C and pressures of 1.7-0.15 kbar. Continuous degassing of melts took place during crystallization. Trace-element concentrations in primary melts were estimated using proton- and ion-probe analyses of melt inclusions in olivine, and whole-rock analyses. Our data suggest that three independent components (D, E1, and E2) were involved. Component D was a refractory mantle depleted in incompatible elements, likely to be hot 'dry' lherzolite produced by previous melting within a mantle plume. Component E1 was an H2O-rich fluid containing LILE and Th, and had an H2O/K2O value of 20; it was probably produced by dehydration of the subducted slab. Component E2 is thought to have been an incompatible-element-enriched silicate melt of plume origin. Formation of high-Ca boninites requires interaction of hot 'dry' residual mantle, associated with plumes, with a subduction-related H2O-bearing component.
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页码:1183 / 1211
页数:29
相关论文
共 83 条
[1]  
[Anonymous], 1989, BONINITES RELATED RO
[2]  
[Anonymous], GEOCHEM INT
[3]  
ARAI S, 1987, NEUES JB MINER MONAT, P347
[4]  
Arai S., 1990, OPHIOLITES OCEANIC C, P557
[5]  
BAKUMENTKO IT, 1975, DEEPSEATED XENOLITHS, P231
[6]   PETROLOGY AND GEOCHEMISTRY OF BONINITE SERIES VOLCANIC-ROCKS FROM THE MARIANA TRENCH [J].
BLOOMER, SH ;
HAWKINS, JW .
CONTRIBUTIONS TO MINERALOGY AND PETROLOGY, 1987, 97 (03) :361-377
[7]   ROLE OF H2O IN SILICATE MELTS .2. THERMODYNAMIC AND PHASE RELATIONS IN SYSTEM NAALSI3O8-H2O TO 10 KILOBARS, 700 DEGREES CENTIGRADE TO 1100 DEGREES CENTIGRADE [J].
BURNHAM, CW ;
DAVIS, NF .
AMERICAN JOURNAL OF SCIENCE, 1974, 274 (08) :902-940
[8]  
BURNHAM CW, 1979, EVOLUTION IGNEOUS RO, P439
[9]  
Cameron W. E., 1989, BONINITES, P314