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1.
Experimental melting relationships for a mafic minette (mica-lamprophyre) from Buell Park, Arizona were determined under fO2 conditions equivalent to the ironwüstite-graphite and quartz-fayalite-magnetite buffers, at pressures of 10–20 kbar. A comparison between experimental products and phenocrysts in the most primitive minettes indicates that those lavas preserve a near-liquidus assemblage of olivine, diopside and Ti-rich phlogopite crystallized in the upper mantle under fO2QFM and in the presence of an H2O-bearing fluid phase. It is suggested that micalamprophyric (minette) magmas may originate from a metasomatized, garnet-bearing peridotitic source at deeper levels in the mantle (P20 kbar) but can also be in equilibrium with a phlogopite-bearing wehrlite (±opx) source at pressures of 17–20 kbar, under reducing or oxidizing mantle conditions. Owing to their rapid crystallization rate and high liquidus temperatures, a series of potassic daughter melts (potassic latites and felsic minettes) can be formed by segregation from mafic minette parents during their ascent through the cooler continental crust. The preservation of olivine in equilibrium with phlogopite phenocrysts in primitive minettes precludes a petrogenetic process dominated by assimilation/fractional crystallization in a shallow magma chamber and supports a model by which some lamprophyric magmas are brought to near surface conditions at temperatures in the range of 1,000–1,200° C and chilled rapidly.  相似文献   

2.
The Jurassic Bangong Lake ophiolite, NW Tibet, is a key element within the western part of the Bangong–Nujiang suture zone, which marks the boundary between the Lhasa and Qiangtang blocks. It is a tectonic mélange consisting of numerous blocks of peridotite, mafic lavas and dikes. The mantle peridotites include both clinopyroxene-bearing and clinopyroxene-free harzburgites. The Cpx-bearing harzburgite contains Al-rich spinel with low Cr#s (20–25), resembling peridotites formed in mid-ocean ridge settings. On the other hand, the Cpx-free harzburgite is highly depleted with Cr-rich spinel (Cr# = 69–73), typical of peridotites formed in subduction zone environments. Mafic rocks include lavas of N-MORB and E-MORB affinity and boninites. The N-MORB rocks consist of pillow lavas and mafic dikes, whereas the E-MORB rocks are brecciated basalts. The boninites have high SiO2 (53.2–57.9 wt%), MgO (6.5–12.5 wt%), Cr (166–752 ppm) and Ni (63–213 ppm) and low TiO2 (0.22–0.37 wt%) and Y (5.34–8.10 ppm), and are characterized by having U-shaped, chondrite-normalized REE patterns. The N-MORB and E-MORB lavas probably formed by different degrees of partial melting of primitive mantle, whereas the boninites reflect partial melting of depleted peridotite in a suprasubduction zone environment. The geochemistry of the ophiolite suggests that it is a fragment of oceanic lithosphere formed originally at a mid-ocean ridge (MOR) and then trapped above an intraoceanic subduction zone (SSZ), where the mantle peridotites were modified by boninitic melts. The Bangong–Nujiang suture zone is believed to mark the boundary between two blocks within Gondwanaland rather than to separate Gondwanaland from Eurasia.  相似文献   

3.
Anhydrous P-T phase relations, including phase compositions and modes, are reported from 10–31 kbar for a near-primary high-alumina basalt from the South Sandwich Islands in the Scotia Arc. The water content of natural subduction-related basalt is probably <0.5 wt.% and thus, these results are relevant to the generation of primary basaltic magmas in subduction zones. At high pressures (>27 kbar) garnet is the liquidus phase followed by clinopyroxene, then quartz/coesite at lower temperatures. At intermediate pressures (17–27 kbar), clinopyroxene is the liquidus phase followed by either garnet, quartz, plagioclase, then orthopyroxene or plagioclase, quartz, garnet, then orthopyroxene depending on the pressure within this interval. At all lower pressures, plagioclase is the liquidus phase followed at much lower temperatures (100° C at 5 kbar) by clinopyroxene. The absence of olivine from the liquidus suggests that the composition studied here could not have been derived from a more mafic parent by olivine fractionation at any pressure investigated, and supports the interpretation that it is primary. If so, these results also preclude an origin for this melt by partial melting of olivine-rich mantle periddotite and suggest instead that it was generated by partial melting of the descending slab (quartz eclogite) leaving clinopyroxene, garnet, or both in the residue. The generally flat REE patterns for low-K series subduction related basalts argue against any significant role for garnet, however, and it is thus concluded that the composition studied here was extracted at 20–27 kbar after sufficiently high degrees of partial melting (50%) to totally consume garnet in the eclogite source. Melting experiments on three MORB composition, although not conclusive, are in agreement with this mechanism. Results at 30 kbar support an origin for tonalite/trondhjemite series rocks by lower degrees of melting (15–30%), leaving both garnet and clinopyroxene in the residue.  相似文献   

4.
Wadeite of composition Zr2K4Si6O18, synthesized at 1 atm, is stable between 12–25 kb at 800 °–1,250 ° C; conditions appropriate to those of partial melting of an anomalous K-enriched upper mantle. If published hypotheses for the generation of high potash mafic to ultramafic lavas based on partial melting of such an anomalous mantle are correct, wadeite is a possible K-bearing mineral, in addition to phlogopide and K-richterite, stable under mantle conditions. The restricted occurrence of wadeite to rocks of West Kimberley, Australia and Leucite Hills, Wyoming is believed to be due to their high K/Al and Zr contents relative to other high potash rocks. The cell constants of wadeite of Zr2K4Si6O18 composition are in agreement with those of natural Zr-rich wadeite and with the values predicted from synthetic wadeites with smaller tetravalents ions in the Zr site.  相似文献   

5.
碧口群火山岩岩石成因研究   总被引：13，自引：1，他引：12  
新元古代(846~776Ma)碧口群火山岩喷发于大陆板内裂谷环境。该火山岩系以基性火山岩为主,酸性火山岩次之,中性火山岩少见。根据岩石地球化学数据,碧口群裂谷基性熔岩总体上属于低Ti/Y(<500)岩浆类型。元素和同位素数据表明,碧口群基性熔岩的化学变化不是由一个共同的母岩浆的结晶分异作用所产生。它们极有可能是源于地幔柱源(εNd(t)≈+3,87Sr/86Sr(t)≈0.704,La/Nb≈0.7)。地壳混染作用对于碧口群裂谷基性熔岩的形成有重要贡献。我们的研究揭示,碧口群火山岩存在空间上的岩石地球化学变化。东部红岩沟和辛田坝—黑木林地区的碧口群基性熔岩以拉斑玄武岩为主,产生于幔源石榴子石稳定区的高度部分熔融。相反,西部白杨—碧口地区的碧口群基性熔岩的母岩浆则是形成于幔源的尖晶石-石榴子石过渡带:碱性熔岩是产生于部分熔融程度较低的条件下,拉斑玄武质熔岩则是产生于部分熔融条件较高的条件下。它们经受了浅层位辉长岩质(cpx+plag±ol)分离作用,化学变异较大。  相似文献   

6.
A wide compositional continuum of basalts has been erupted from near-ridge seamounts constructed on the Cocos Plate between the Clipperton and Orozco Francture Zones. They range from highly evolved to moderately primitive (3.0–7.8% MgO), LREE-enriched alkali basalts, to moderately evolved to near-primary (5.2–9.5% MgO) tholeiites indistinguishable from N-type MORB. The data set of 159 quench glass analyses exhibits a remarkably consistent variation in both major and trace element composition that is keyed to variations in (La/Sm). Modeling of potential liquid lines of descent at pressures ranging from 1 bar to 8 kbar shows that this covariation is partially due to systematic differences in liquid lines of descent, where the alkaline lavas have undergone substantially more high pressure clinopyroxene fractionation and substantially less low pressure plagioclase fractionation than the tholeiites. In addition, systematic variation in the composition of the more primitive glasses indicates that they were derived from mixing of discrete enriched and depleted melts in the heterogenous seamount mantle source at pressures of 8–10 kbar and greater, and that clinopyroxene may be a residual phase during partial melting. These results show that porous media flow in the seamount mantle source is minor and that melt transport is accomplished primarily through cracking and diking. This study supports suggestions that the general homogeneity of basalt along the EPR is due to mixing in sub-axial magma chambers and mush zones, with additional mixing during partial mantle melting and melt segregation.  相似文献   

7.
Alan R. Hastie  Andrew C. Kerr 《Earth》2010,98(3-4):283-293
The Caribbean oceanic plateau formed in the Pacific realm when it erupted onto the Farallon plate from the Galapagos hotspot at ～ 90 Ma. The plateau was subsequently transported to the northeast and collided with the Great Arc of the Caribbean thus initiating subduction polarity reversal and the consequent tectonic emplacement of the Caribbean plate between the North and South American continents. The plateau represents a large outpouring of mafic volcanism, which has been interpreted as having formed by melting of a hot mantle plume. Conversely, some have suggested that a slab window could be involved in forming the plateau. However, the source regions of oceanic plateaus are distinct from N-MORB (the likely source composition for slab window mafic rocks). Furthermore, melt modelling using primitive (high MgO) Caribbean oceanic plateau lavas from Curaçao, shows that the primary magmas of the plateau contained ～ 20 wt.% MgO and were derived from 30 to 32% partial melting of a fertile peridotite source region which had a potential temperature (Tp) of 1564–1614 °C. Thus, the Caribbean oceanic plateau lavas are derived from decompression melting of a hot upwelling mantle plume with excess heat relative to ambient upper mantle. Extensional decompression partial melting of sub-slab asthenosphere in a slab window with an ambient mantle Tp cannot produce enough melt to form a plateau. The formation of the Caribbean oceanic plateau by melting of ambient upper mantle in a slab window setting, is therefore, highly improbable.  相似文献   

8.
K, Na and Ca are the most common elements transported during mantle metasomatism and result in formation of phlogopite (K), amphibole (Na) and clinopyroxene (Ca) by various reactions. This review presents models for this type of metasomatism based on experiments on the pyrolite-K2CO3-H2O, pyrolite-Na2 CO3-H2O systems and on the pyrolite-CaCO3 system. The addition of K2CO3 and Na2CO3 lowers the liquidus of pyrolite providing a low temperature, alkali-rich hydrous melt which may ascend and metasomatize overlying mantle regions. Several reactions are proposed for the formation of phlogopite and amphibole (pargasite-edenite) in these systems. The compositions of amphiboles correspond to those found in metasomatized mantle xenoliths. In contrast, Ca-metasomatism is considered to be mainly an anhydrous process in which orthopyroxene and carbonate react to produce clinopyroxene, olivine and CO2. High pressure liquids in this model system are of carbonatitic composition and this low viscosity melt can ascend converting harzburgite mantle assemblages to olivine-rich wehrlite. Based on an inverse experimental approach, moderately high degrees of partial melting of a model metasomatized alkali clinopyroxenite xenolith yield liquids at 30kb which are very comparable in composition to the lavas enclosing such types of xenoliths. Experimental modelling of mantle metasomatism produces assemblages which are in good agreement with the mineral assemblages and textural relationships found in metasomatized mantle xenoliths from areas such as West Eifel and South-West Uganda.  相似文献   

9.
Compositions of the major phenocryst minerals (olivine, phlogopite) and groundmass minerals (olivine, phlogopite, kalsilite), and a glass phase have been determined from a biotite mafurite occurring as an ejected block in the highly K-rich ultramafic rocks of south west Uganda. Comparison of the phenocryst mineral compositions with those determined from recent high pressure experiments on biotite mafurite composition suggests this rock may have formed by partial melting of a K-enriched mantle source containing both H2O and CO2 at approximately 1,250 ° C and 30 kb. The absence of crystalline leucite but its presence as a major component of the glass phase and textural relations in the groundmass indicate that the final consolidation of the biotite mafurite took place at pressures greater than atmospheric. The presence of phlogopite, olivine, kalsilite, and glass mainly of leucite composition may suggest that consolidation took place under the conditions where these phases were in equilibrium. Based on the experimentally determined conditions for the reaction of phlogopite break down to olivine+kalsilite +liquid+vapor, a crude estimation of the consolidation conditions for ejected blocks of biotite mafurite are 1,150 °–1,180 ° C at a of 1–2 kb.  相似文献   

10.
D.H. Green 《Tectonophysics》1973,17(3):285-297
The pyrolite model composition provides a satisfactory source composition for mantle-derived magmas insofar as major elements and “compatible” trace elements are concerned but there is evidence for mantle inhomogeneity in the abundances of “incompatible” minor and trace elements (e.g., K, Ti, P, Rb, Sr, light rare earth elements etc.). The composition of a magma, assuming a constant source composition, varies according to the pressure, temperature and water pressure or water content of the source region. The latter two variables essentially determine the degree of partial melting of the source region and in considering the chemical composition of the melt and nature of the residual phases, this parameter is of prime importance.For high degrees (> 20% approx.) of partial melting of a pyrolite source region, magmas are of tholeiitic character but are of increasingly undersaturated and alkaline type for lower degrees of partial melting and high pressures. For any chosen degree of melting and fixed water content of the source region, magmas are more olivine-rich at higher pressures. For any chosen pressure and chosen degree of partial melting, magmas are less olivine-rich at high water contents (and thus lower temperatures). Quartz tholeiite magmas may be derived by ~ 30% melting of pyrolite under water-saturated conditions at pressures up to between 17 kbar and 20 kbar. These generalizations may be applied to understand the characteristic magmatism of mid-oceanic ridges, island chains, oceanic islands and orogenic regions.  相似文献   

11.
The water-undersaturated melting relationships of a mafic, peralkaline, potassic madupite (with about 3% H2O as shown by chemical analysis) from the Leucite Hills, Wyoming, have been studied at pressures up to 30 kb. At low pressures (<5 kb) leucite is the dominant liquidus phase, but it is replaced at higher pressures by clinopyroxene plus olivine (<5–7 kb), clinopyroxene (7–12.5 kb), clinopyroxene plus minor spinel (12.5–17.5 kb), and clinopyroxene alone (17.5–> 30 kb). At all pressures there is a reaction relationship with falling temperature between melt, olivine and probably clinopyroxene to yield phlogopite. Apatite is stable within the melting interval to pressures above 25 kb. Electron microprobe analyses demonstrate that the clinopyroxene is diopsidic, with low aluminium and titanium contents. Pressure has relatively little effect on the composition of the pyroxene. Phlogopite is also aluminium-poor and has only a moderate titanium content. The experimental results indicate that madupite is not the partial melting product of hydrous lherzolite or garnet lherzolite in the upper mantle and it seems improbable that it is derived by melting of mantle peridotite with a mixed H2O-CO2 volatile component. Madupite could, however, be the partial melting product of mica-pyroxenite or mica-olivine-pyroxenite in the upper mantle. It is pointed out that the chemistry of some potassium-rich volcanics may have been affected by volatile transfer and other such processes during eruption and that experimental studies of material affected in this way have little bearing upon the genesis of potassic magmas. Finally, the experimental results enable constraints to be placed upon the P-T conditions of the formation of richterite-bearing mica nodules found in kimberlites and associated rocks. Maximum conditions are 25 kb and 1,100 ° C.  相似文献   

12.
The Mafic and Ultramafic Lavas of the Belingwe Greenstone Belt, Rhodesia   总被引：3，自引：3，他引：3  
The Belingwe Greenstone Belt (2.8 x 109 yrs old) contains a7 km succession of mafic and ultramafic lavas and high-levelintrusions which overlie a thin sedimentary formation, itselfunconformable on a granitic basement. The lavas range in compositionfrom andesites (4 per cent MgO) to peridotitic komatiites (32per cent MgO). The mineralogy and textures of the most magnesianlavas demonstrate that they were extruded in a completely liquidstate. If the source mantle had an MgO content around 40 percent, then partial melts in the range 35 per cent to 55 percent would be required to produce the most magnesian liquidsobserved. Chemical constraints on the petrogenesis of the ultramafic lavasallow estimates of source mantle composition. In particular,if the source had an MgO content around 40 per cent, then theoverall source composition would be similar to that of garnetIherzolite nodules in kimberlites. The calculated REE contentsof the source are close to chondritic. If all the ultramaficlavas were derived from the same source then the variation inliquid composition may have been controlled by orthopyroxeneas well as olivine during partial melting at depth. The evolutionof the less magnesian komatiites, basalts, and andesites canbe explained by lower degrees of partial melting of a commonsource, and by high-level fractionation of parent liquids similarto those extruded as ultramafic lavas. Physical constraints on the origin of the lavas imply derivationfrom a depth of 150 km or more, at temperatures of 1600–2000°C.  相似文献   

13.
Since Mesozoic time, Java and Bali have formed part of an evolving system of island arcs comprising the Sunda arc of Indonesia. The present tectonic setting is relatively simple with subduction occurring at the Java Trench to the south. A north-dipping Benioff seismic zone delineates an underthrust lithospheric slab to depths of approximately 600 km beneath the Java Sea. Quaternary lavas of the normal island arc association range from tholeiites to high-K calc-alkaline lavas over Benioff zone depths from 120–250 km, respectively. More abundant calc-alkaline lavas lie between these extremes. High-K alkaline lavas are found over Benioff zone depths in excess of 300 km.Both within and between these groups of rocks there are consistent spatial variations in the observed geochemistry. For approximately 200 rocks, incompatible elements such as K, Rb, Cs, Sr, Ba, light REE, U and Th show an increase in abundance of almost an order of magnitude with increasing depth to the seismic zone. Abundances of compatible elements show little consistent variation and trace elements such as Ni, Co, Cr, and Sc are characteristically depleted except in some of the alkaline lavas. Major element abundances in rocks of the normal island arc association show little variation, except for K and P, which both increase in abundance across the arc and Al, which shows a relative decrease.The major and trace element data are inconsistent with the derivation of the analyzed rocks by partial melting of the crustal component of the subducted lithosphere. On the other hand, low Ni abundances (20 ppm) in the basalts suggest that most of the lavas are fractionated and few if any represent primary mantle-derived melts. The spatial variations in the geochemistry of erupted lavas across Java and Bali are best explained by a combination of two processes: melting of a geochemically zoned mantle source and smaller degrees of partial melting of that material at progressively greater depths. Primary tholeiitic magmas could be formed by 20–25% melting at depths of 30–40 km, primary high-K calc-alkaline magmas by 5–15% melting at 40–60 km depth, and primary alkaline magmas by 5% melting at depths of 80–90 km. The geochemical zoning in the mantle, which is also manifested by increasing 87Sr/86Sr ratios in lavas across the arc, is interpreted to result from the addition of a small melt fraction derived from the crustal component of the subducted lithosphere.  相似文献   

14.
Ultrabasic magmas and high-degree melting of the mantle   总被引：1，自引：0，他引：1  
As the degree of melting of mantle peridotite increases, the liquids that are formed become more basic and less viscous, and the spacing between residual crystals increases. The settling velocities of residual crystals in partial melts consequently will increase by several orders of magnitude, from 9.4 × 10–4 cm/s to 4.3 × 10–1 cm/s for a 1 cm olivine grain, as the proportion of liquid increases from 15 to 60%.To produce an ultrabasic komatiitic magma from a source with commonly assumed mantle composition requires 50 to 80% melting. Before this degree of melting can be reached, a highly fluid picritic magma produced by 30 to 50% melting will segregate from the source. Ultrabasic magmas probably form by a sequential melting process and are derived from a residuum composed of refractory minerals and trapped liquid left by previous episodes of partial melting and magma extraction. Trace element concentrations in ultrabasic komatiite lavas are consistent with this theory.  相似文献   

15.
Amphibole-bearing mafic inclusions (low to medium-K high-alumina basalt to basaltic andesite) comprise 4.1 vol% of calc-alkaline rhyolite and rhyodacite lavas on Akrotiri Peninsula, Santorini, Greece. Physical features indicate a magmatic origin for the inclusions, involving mingling with the host silicic magma and quenching. Water contents of the mafic magmas are estimated to have been above 4% at water pressures of 1.8 kbars or more at temperatures of approximately 950–1,000 °C. Three evolutionary stages are inferred in their petrogenesis. In the first stage infiltration of slab fluids promotes partial melting in the mantle to generate primitive wet basaltic magmas enriched in LREE, LILE, Th and U in comparison to N-type MORB. In the second stage storage and crystal differentiation of primitive magmas occurred in the lithospheric mantle or deep crust, involving olivine, spinel and clinopyroxene followed by amphibole and plagioclase. In the third stage differentiated mafic magma intrudes into porphyritic silicic magma at shallower crustal levels (estimated at 7–10 km). Mingling and quenching of the mafic magmas within the silicic host causes chemical or physical interactions between the inclusions and the host prior to and during eruption. The silicic lavas have geochemical affinities with the mafic inclusions, but are relatively depleted in MREE, HREE and Y and enriched in Rb relative to Ba and K. These observations are consistent with involvement of amphibole in magma genesis due either to crystal differentiation from wet basalt or to partial melting of mafic rocks with residual amphibole. Crystallization of wet basalt in the deep crust is preferred on the basis of physical considerations.Electronic Supplementary Material Supplementary material is available for this article if you access the article at . A link in the frame on the left on that page takes you directly to the supplementary material.Editorial responsibility: I. Parsons  相似文献   

16.
Process identification diagrams based on trace element data show that mafic lavas from Tubuai, including alkali basalts, basanites, analcitites and nephelinites, result from different degrees of partial melting of an isotopically homogeneous mantle source. Our fractionation-corrected data are consistent with a batch melting model or a dynamic melting model involving a threshold value for melt separation close to 1% and degrees of melting ranging from 5–8% (alkali basalts) to 1.5–3% (nephelinites). The relative source concentration pattern, calculated using an inverse numerical method, shows an enrichment in highly incompatible elements. We propose that the Tubuai lava suite was derived from a two-stage partial melting process. Melting first affected the plume material located within the transition zone between garnet and spinel domains, producing alkali basalts and basanites. Then, the melting zone migrated upwards to the base of the overlying spinel-bearing lithospheric mantle, producing highly silica-undersaturated lavas. The lower lithosphere had previously been enriched by intrusion of pyroxenite veins representing plume-derived melts which percolated away from the main magma conduits. Received: 11 June 1996 / Accepted: 8 January 1997  相似文献   

17.
The Cape Verde islands are characterized by the presence of very strongly alkalic lavas. Cenozoic volcanics—covering the broadest compositional range present in the archipelago—and ranging from alkali-basalts to phonolites, associated with plutonic essexites and nepheline syenites, were analyzed for Sr isotopic compositions and concentrations in K, Rb and Sr. The close values of the Sr87/Sr86 ratios (ranging from 0.7029 to 0.7033) indicate a comagmatic origin for the different rock types; no correlation appears between the Sr isotopic composition and the K-content of the lavas, thus indicating that the lavas with high K2O/K2O + Na2O ratio are generated from a primary magma by differentiation at shallow depths. The values of the Sr isotopic composition are distinctly lower than most values obtained for lavas of other oceanic islands. The origin of the magma type is discussed on the basis of these isotopic compositions and the K/Rb and Rb/Sr ratios: it is suggested that the primary magma has a nephelinitic composition and was formed by partial melting of a small fraction of undepleted mantle peridotite, containing phlogopite; the deeper part of the mantle where this nephelinitic magma generates would have a strontium isotopic ratio of about 0.703 and a Rb/Sr ratio lower than that of the upper part.  相似文献   

18.
This study presents new geochemical data on rocks from the Vespor suite, an important mafic unit from the Juruena arc, Roosevelt-Juruena terrain, SW Amazonian craton, northwest Mato Grosso, Brazil, attempting to define their tectonic setting and type of mantle source. The Juruena arc may be part of a magmatic belt (Jamari and Juruena arcs) at the southwestern Amazonian craton during assembly of the Columbia supercontinent. The investigated rocks represent a Paleoproterozoic subduction-related mafic suite of sigmoidal bodies, composed mainly of gabbro, norite, gabbronorite and diorite, that underwent amphibolite facies metamorphism. Here we present also preliminary petrology aspects and zircon U–Pb geochronology. Geochemical character and variation trends of major and trace elements as well as selected trace element ratios suggest that Vespor suite rocks have a tholeiitic lineage of arc affinity controlled by fractional crystallization with a prominent iron enrichment trend. Gabbros, norites and gabbronorites are characterized by enrichment of LILE and weakly to moderately differentiated HFSE patterns, suggesting their deviation from an enriched heterogeneous lithospheric mantle source. Vespor suite rocks are characterized by depletion of Nb–Ta, P and Ti, with flat distribution of HFSE, markedly large variations in most of the LILE, positive anomalies displayed by Ba, K, Th, Sr, Pb and weak negative anomalies of Hf–Zr. These features reflect limited degrees of crustal contamination associated with a subduction-related magma process where the mantle wedge was chemically modified. In addition, the enrichment in LILE and Pb, low values of the ratios (Lan/Smn – 0.83 to 4.58) and (Nbn/Lan – 0.04 to 0.45), but high Th/Yb ratios, gently to moderately sloping REE profiles (La/Ybn = 2.53–7.37), negative anomalies in HFSE (Ta, Zr, Hf, and Ti), and positive anomalies in LILE (Th, Ba, Sr), suggest derivation from a metasomatized lithospheric mantle source above a subduction zone with weak crustal contamination. Both the composition of the mantle source and the degree of partial melting that produced the parental magmas of these rocks, determined by using REE abundance and ratios, indicate that gabbroic/dioritic melts were generated at different degrees of melting of the source: about 5–20% partial melting of a garnet-spinel lherzolite, around 1–10% partial melting of spinel lherzolite source, and approximately 1–5% partial melting of intermediate source composition, and crystallizing between 1.773 and 1.764 Ma.  相似文献   

19.
Five mafic lava flows located on the southern flank of Mount Baker are among the most primitive in the volcanic field. A comprehensive dataset of whole rock and mineral chemistry reveals the diversity of these mafic lavas that come from distinct sources and have been variably affected by ascent through the crust. Disequilibrium textures present in all of the lavas indicate that crustal processes have affected the magmas. Despite this evidence, mantle source characteristics have been retained and three primitive endmember lava types are represented. These include (1) modified low-K tholeiitic basalt (LKOT-like), (2) typical calc-alkaline (CA) lavas, and (3) high-Mg basaltic andesite and andesite (HMBA and HMA). The Type 1 endmember, the basalt of Park Butte (49.3–50.3 wt% SiO2, Mg# 64–65), has major element chemistry similar to LKOT found elsewhere in the Cascades. Park Butte also has the lowest overall abundances of trace elements (with the exception of the HREE), indicating it is either derived from the most depleted mantle source or has undergone the largest degree of partial melting. The Type 2 endmember is represented by the basalts of Lake Shannon (50.7–52.6 wt% SiO2, Mg# 58–62) and Sulphur Creek (51.2–54.6 wt% SiO2, Mg# 56–57). These two lavas are comparable to calc-alkaline rocks found in arcs worldwide and have similar trace element patterns; however, they differ from each other in abundances of REE, indicating variation in degree of partial melting or fractionation. The Type 3 endmember is represented by the HMBA of Tarn Plateau (51.8–54.0 wt% SiO2, Mg# 68–70) and the HMA of Glacier Creek (58.3–58.7 wt% SiO2, Mg# 63–64). The strongly depleted HREE nature of these Type 3 units and their decreasing Mg# with increasing SiO2 suggests fractionation from a high-Mg basaltic parent derived from a source with residual garnet. Another basaltic andesite unit, Cathedral Crag (52.2–52.6 wt% SiO2, Mg# 55–58), is an Mg-poor differentiate of the Type 3 endmember. The calc-alkaline lavas are least enriched in a subduction component (lowest H2O, Sr/PN, and Ba/Nb), the LKOT-like lavas are intermediate (moderate Sr/PN and Ba/Nb), and the HMBA are most enriched (highest H2O, Sr/PN and Ba/Nb). The generation of the LKOT-like and calc-alkaline lavas can be successfully modeled by partial melting of a spinel lherzolite with variability in composition of slab flux and/or mantle source depletion. The HMBA lavas can be successfully modeled by partial melting of a garnet lherzolite with slab flux compositionally similar to the other lava types, or less likely by partial melting of a spinel lherzolite with a distinctly different, HREE-depleted slab flux.  相似文献   

20.
Three linear zones of active andesite volcanism are present in the Andes — a northern zone (5°N–2°S) in Colombia and Ecuador, a central zone (16°S–28°S) largely in south Peru and north Chile and a southern zone (33°S–52°S) largely in south Chile. The northern zone is characterized by basaltic andesites, the central zone by andesite—dacite lavas and ignimbrites and the southern zone by high-alumina basalts, basaltic andesites and andesites. Shoshonites and volcanic rocks of the alkali basalt—trachyte association occur at scattered localities east of the active volcanic chain,The northern and central volcanic zones are 140 km above an eastward-dipping Benioff zone, while the southern zone lies only 90 km above a Benioff zone. Continental crust is ca. 70 km in thickness below the central zone, but is 30–45 km thick below northern and southern volcanic zones. The correlation between volcanic products and their structural setting is supported by trace element and isotope data. The central zone andesite lavas have higher Si, K, Rb, Sr and Ba, and higher initial Sr isotope ratios than the northern or southern zone lavas. The southern zone high-alumina basalts have lower Ce/Yb ratios than volcanics from the other zones. In addition, the central zone andesite lavas show a well-defined eastward increase in K, Rb and Ba and a decrease in Sr.Andean andesite magmas are a result of a complex interplay of partial melting, fractional crystallization and “contamination” processes at mantle depths, and contamination and fractional crystallization in the crust. Variations in andesite composition across the central Andean chain reflect a diminishing degree of partial melting or an increase in fractional crystallization or an increase in “contamination” passing eastwards. Variations along the Andean chain indicate a significant crustal contribution for andesites in the central zone, and indicate that the high-alumina basalts and basaltic andesites of the southern zone are from a shallower mantle source region than other volcanic rocks. The dacite-rhyolite ignimbrites of the central zone share a common source with the andesites and might result from fractional crystallization of andesite magma during uprise through thick continental crust. The occurrence of shoshonites and alkali basalts eat of the active volcanic chain is attributed to partial melting of mantle peridotite distant from the subduction zone.  相似文献   

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