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1.
Mantle xenoliths in within-plate Cenozoic alkaline mafic lavas from NE Spain are used to assess the local subcontinental lithospheric mantle geotherm and the influence of melting and metasomatism on its oxidation state. The xenoliths are mainly anhydrous spinel lherzolites and harzburgites and gradations between, with minor pyroxenites. Most types show protogranular textures, but transitional protogranular–porphyroclastic and equigranular lherzolites also exist. Different thermometers used in the estimates provide higher subsolidus equilibrium temperatures for harzburgites (1,062 ± 29°C) than for lherzolites (972 ± 89°C), although there is overlap; the lowest temperatures correspond to porphyroclastic lherzolites, whereas pyroxenites give the highest temperatures (up to 1,257°C). Maximum pressures for subsolidus equilibrium of peridotites are at 2.0–1.8 GPa. Later they followed adiabatic decompression and harzburgites registered lower pressures (1.02 ± 0.19 GPa) than lherzolites (1.41 ± 0.27 GPa). One pyroxenite gives values consistent with the spinel lherzolite field (1.08 GPa). The shallowest barometric data are in agreement with the highest local conductive geotherms, which implies that the lithosphere–asthenosphere boundary is at 70–60 km minimum depth. Higher equilibrium temperatures for the harzburgites could be explained by the existence of mafic magma bodies or dykes at the lower crust–mantle boundary. Paleo-fO2 conditions during partial melting as inferred from the covariation between V and MgO concentrations are mainly between QFM−1 and QFM−2 in log units. However, most thermobarometric fO2 estimates are between QFM−1 and QFM+1, suggesting oxidation caused by later metasomatism during uplift and cooling.  相似文献   

2.
Deep-seated xenoliths entrained in the Hannuoba basalts of the northern Sino-Korean Craton include mafic and felsic granulites, mantle wall-rock from spinel– and garnet–spinel peridotite facies, and basaltic crystallisation products from the spinel-pyroxenite and garnet-pyroxenite stability fields. The mineral compositions of the xenoliths have been used to estimate temperatures and, where possible, pressures of equilibration, and to construct a geothermal framework to interpret the upper mantle and lower crustal rock-type sequences for the region. The xenolith-derived paleogeotherm is constrained in the depth interval of 45–65 km and like others from areas of young basalt magmatism, is elevated and strongly convex toward the temperature axis. Two-pyroxene granulites give the lowest temperatures and garnet pyroxenites the highest, while the spinel lherzolites fall between these two groups. The present-day Moho beneath the Hannuoba area is defined at 42 km by seismic data, and coincides with the deepest occurrence of granulite. Above this boundary, there is a lower crust–upper mantle transition zone about 10-km thick, in which spinel lherzolites and mafic granulites (with variable plagioclase contents) are intermixed. It is inferred that this underplating has resulted in a lowering of the original pre-Cenozoic Moho (then coinciding with the crust–mantle boundary, CMB) from about 30 km to its present-day position and was due to intrusions of basaltic magmas that displaced peridotite mantle wall-rock and equilibrated to mafic granulites. Trace element patterns of the diopsides (analysed by laser ablation-ICPMS) from the Cr-diopside series spinel lherzolites and associated layered xenoliths (spinel lherzolites and pyroxenites) indicate a fertile uppermost mantle with moderate depletion by low degrees of partial melting and little evidence of metasomatic activity. The similarity in major and trace element compositions of the minerals in both rock types suggests that the layered ultramafic xenoliths formed by mantle deformation processes (metamorphic segregation), rather than by melt veining or metasomatism.  相似文献   

3.
High-temperature peridotite massifs occur as lensoid bodies with high-pressure granulites in the southern Bohemian massif. In lower Austria the peridotites comprise garnet lherzolites lacking primary spinel, rare garnet and garnet-spinel harzburgites, and harzburgites containing Cr-rich primary spinel instead of garnet. These phase assemblages suggest initial high-pressure equilibration and are consistent with results from garnet-orthopyroxene geobarometry indicating equilibration at around 3–3.5 GPa. Maximum temperature estimates obtained on core compositions of coexisting minerals from the peridotites are not higher than ca. 1100 °C. In contrast, pyroxene megacryst compositions, garnet exsolution textures in the garnet pyroxenites, and results from geothermometry indicate much higher original equilibration temperatures in most of the pyroxenites (up to 1400 °C). High temperatures, modal zoning, the occasional presence of Mg-rich garnetites and chemical evidence suggest that the pyroxenites are cumulates which crystallized from low-degree melts derived from the sub-lithospheric mantle. Isothermal interpolation of the high temperatures to an upper mantle adiabat suggests that the melts were derived from a minimum depth of 180–200 km. The formation of small garnet II grains and garnet exsolution lamellae in the pyroxenites and pyroxene megacrysts may reflect isobaric cooling of the cumulates from temperatures above 1400 °C to ca. 1100–1200 °C (at 3–3.5 GPa) to approach the ambient lithospheric isotherm. This model differs from other models in which the formation of garnet II was explained by an increase in pressure during cooling in a subduction zone. Isobaric cooling was followed by near-isothermal decompression from 3–3.5 GPa to 1.5–2 GPa at 1000–1200 °C, as indicated by the increase of Al in pyroxenes near garnet. Further cooling in the spinel lherzolite stability field is indicated by spinel exsolution lamellae in pyroxenes from lherzolites. The formation of symplectites and kelyphites indicate sub-millimetre scale re-equilibration during exhumation in the course of the Carboniferous collision in the Bohemian massif. The peridotite massifs represent fragments of normal (non-cratonic) lithospheric mantle from a Paleozoic convergent plate margin. Received: 22 July 1996 / Accepted 28 February 1997  相似文献   

4.
Mantle derived xenoliths in India are known to occur in the Proterozoic ultrapotassic rocks like kimberlites from Dharwar and Bastar craton and Mesozoic alkali igneous rocks like lamrophyres, nephelinites and basanites. The xenoliths in kimberlites are represented by garnet harzburgites, lherzolites, wehrlite, olivine clinopyroxenites and kyaniteeclogite varieties. The PT conditions estimated for xenoliths from the Dharwar craton suggest that the lithosphere was at least 185 km thick during the Mid-Proterozoic period. The ultrabasic and eclogite xenoliths have been derived from depths of 100–180 km and 75–150 km respectively. The Kalyandurg and Brahmanpalle clusters have sampled the typical Archaean subcontinental lithospheric mantle (SCLM) with a low geotherm (35 mW/m2) and harzburgitic to lherzolitic rocks with median Xmg olivine > 0.93. The base of the depleted lithosphere at 185–195 km depth is marked by a 10–15 km layer of strongly metasomatised peridotites (Xmg olivine > ∼0.88). The Anampalle and Wajrakarur clusters 60 km to the NW show a distinctly different SCLM; it has a higher geotherm (37.5 to 40 mW/m2) and contains few subcalcic harzburgites, and has a median Xmg olivine = 0.925. In contrast, the kimberlites of the Uravakonda and WK-7 clusters sampled quite fertile (median Xmg olivine ∼0.915) SCLM with an elevated geotherm (> 40 mW/m2). The lamrophyres, basanites and melanephelinites associated with the Deccan Volcanic Province entrain both ultramafic and mafic xenoliths. The ultramafic group is represented by (i) spinel lherzolites, harzburgites, and (ii) pyroxenites. Single pyroxene granulite and two pyroxene granulites constitutes the mafic group. Temperature estimates for the West Coast xenoliths indicate equilibration temperatures of 500–900°C while the pressure estimates vary between 6–11 kbar corresponding to depths of 20–35 km. This elevated geotherm implies that the region is characterized by abnormally high heat flow, which is also supported by the presence of linear array of hot springs along the West Coast. Spinel peridotite xenoliths entrained in the basanites and melanephelinites from the Kutch show low equilibrium temperatures (884–972°C). The estimated pressures obtained on the basis of the absence of both plagioclase and garnet in the xenoliths and by referring the temperatures to the West Coast geotherm is ∼ 15 kbar (40–45 km depth). The minimum heat flow of 60 to 70 mW/m2 has been computed for the Kutch xenolith (Bhujia hill), which is closely comparable to the oceanic geotherm. Xenolith studies from the West Coast and Kutch indicate that the SCLM beneath is strongly metasomatised although the style of metasomatism is different from that below the Dharwar Craton.  相似文献   

5.
Clinopyroxene-rich, poorly metasomatised spinel lherzolites are rare worldwide but predominate among xenoliths in five Quaternary basaltic eruption centres in Tariat, central Mongolia. High-precision analyses of the most fertile Tariat lherzolites are used to evaluate estimates of primitive mantle compositions; they indicate Mg#PM = 0.890 while lower Mg# in the mantle are likely related to metasomatic enrichments in iron. Within a 10 × 20 km area, and between ~45 and ≥60 km depth, the sampled xenoliths suggest that the Tariat mantle does not show km-scale chemical heterogeneities and mainly consists of residues after low-degree melt extraction at 1–3 GPa. However, accessory (<1%) amphibole and phlogopite are unevenly distributed beneath the eruption centres. Ca abundances in olivine are controlled by temperature whereas Al and Cr abundances also depend on Cr/Al in coexisting spinel. Comparisons of conventional and high-precision analyses obtained for 30 xenoliths show that high-quality data, in particular for whole-rocks and olivines, are essential to constrain the origin of mantle peridotites. Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users.  相似文献   

6.
Ultramafic xenoliths were found in recent alkali basalts from São Tomé Island. These include spinel peridotites (lherzolites, harzburgites and dunites) and pyroxenites (orthopyroxenites and clinopyroxenites). Textures and mineral compositions indicate that pyroxenites originated from crystal/liquid separation processes operating on magmas similar to those giving rise to their present host rocks whereas spinel peridotite xenoliths had an accidental origin; Fo (>89) and Ni (>0.36 wt.%) contents in olivines, Mg# (91–95) of orthopyroxenes and low Ti in clinopyroxene (primary crystals: TiO2<0.06 wt.%) and in spinel (TiO2<0.1 wt.%) are within the range reported for abyssal peridotites, indicating São Tomé spinel peridotites represent refractory residues of melting. Nevertheless, the lack of correlation between mineral chemistry and modal composition suggests that spinel peridotite xenoliths are not simple residues and were affected by infiltration of fluid/melts within the mantle. The wide temperature range obtained for spinel peridotites (700 to >1150 °C) is compatible with a long period of pre-entrainment cooling supporting Fitton's [Tectonophysics 94 (1983) 473] hypothesis that proposes oceanic lithosphere uprising in the Cameroon Volcanic Line prior to the initiation of the current thermal regime, related to São Tomé magmatism. The association of upper mantle (peridotite) xenoliths with igneous cumulates (pyroxenites) suggests that the spinel peridotite suite originated in the uppermost mantle above the São Tomé magma storage zone(s), probably in a region of high strain rate, near the boundary between the mantle and the overlying oceanic crust.  相似文献   

7.
In peridotites, olivine, clinopyroxene, and orthopyroxene are complex solid solutions with wide stability fields. Depending mostly on bulk composition and pressure, these minerals may be accompanied by plagioclase (low pressure), spinel (moderate pressure), or garnet (high pressure), resulting in 4-phase and rarer 5-phase assemblages. Although a particular mineral assemblage is stable over a range of P–T, the compositions of the individual minerals vary with changing P–T conditions. Application of standard geothermobarometers to olivine–clinopyroxene–orthopyroxene–spinel peridotites is problematic. An alternative approach is to use a bulk rock composition to calculate equilibrium phase diagrams to determine the conditions under which a particular assemblage is stable. This requires consideration of the 7-component system SiO2–Al2O3–Cr2O3–FeO–MgO–CaO–Na2O, internally consistent thermodynamic data for end members, and reliable mixing models for all mineral solutions. Experimental studies in simpler systems, and solution models from the literature, permit derivation of multicomponent thermodynamic mixing models for the key minerals. The models, when applied to xenoliths from Kilbourne Hole, constrain P and T of equilibration and are less sensitive to mineral compositional variations, or uncertainty in activity models, than standard thermobarometry. Our modeling provides the first tightly constrained pressure estimates for Kilbourne Hole, placing the xenoliths in the spinel stability field at depths (30–45 km) that correspond to the uppermost mantle beneath the Rio Grande Rift. The fine-grained equigranular lherzolite, porphyroclastic lherzolite, and some harzburgite-dunite specimens equilibrated at average conditions of 11.5 Kbar-930°C, 12 Kbar-990°C, and 13 Kbar-1,080°C, respectively. The mantle beneath the Rio Grande Rift is layered; the fine-grained equigranular lherzolite derives from relatively shallow depth (35 km average), and the porphyroclastic lherzolite from slightly deeper levels. Lying 5–10 km beneath both lherzolites, the harzburgite-dunite represents a depth where melt extraction has significantly altered mantle chemistry and where local thermodynamic equilibrium has not been maintained.  相似文献   

8.
Upper mantle xenoliths from the southern Rio Grande rift axis (Potrillo and Elephant Butte) and flank (Adam’s Diggings) have been investigated to determine chemical depletion and enrichment processes. The variation of modal, whole rock, and mineral compositions reflect melt extraction. Fractional melting is the likely process. Fractional melting calculations show that most spinel peridotites from rift axis locations have undergone <5% melting versus 7–14% melting for xenoliths from the rift shoulder, although the total range of fractional melting overlaps at all three locations. In the rift axis, deformed (equigranular and porphyroclastic texture) spinel peridotites are generally characterized by significantly less fractional melting (2–5%) than undeformed (protogranular) xenoliths (up to 16%). This difference may reflect undeformed xenoliths being derived from greater depths and higher temperatures than deformed rocks. Spinel peridotites from the axis and shoulder of the Rio Grande rift have undergone mantle metasomatism subsequent to melt extraction. Under the rift shoulder spinel peridotites have undergone both cryptic and patent (modal) metasomatism, possibly during separate events, whereas the upper mantle under the rift axis has undergone only cryptic metasomatism by alkali basaltic magma.  相似文献   

9.
Coarse-grained, granular spinel lherzolites xenoliths from the Premier kimberlite show evidence of melt extraction and metasomatic enrichment, documenting a complex history for the shallow mantle beneath the Bushveld complex. Compositions of orthopyroxene, clinopyroxene and spinel indicate equilibration within the spinel–peridotite facies of the upper mantle, at depths from 80 to 100 km and temperatures from 720 to 850 °C. Bulk compositions have lower Mg-number [atomic 100 Mg/(Mg + Fe*)] than previously studied spinel peridotites from Premier, and have higher Mg/Si than low-temperature coarse grained garnet lherzolites, suggesting shallower melting conditions or metasomatic enrichment. Clinopyroxene in one sample is highly LREE-depleted indicating very minor modification of a residue of 20% melt extraction, whereas the calculated REE pattern for a melt in equilibrium with a mildly LREE-depleted sample is similar to MORB or late Archean basalt, possibly related to the Bushveld Complex. Bulk and mineral compositions suggest minimal refertilization by silicate melts in four out of six samples, but REE patterns indicate introduction of a LIL-enriched component that may be related to kimberlite.  相似文献   

10.
Neogene basanite lavas of Kozákov volcano, located alongthe Lusatian fault in the northeastern Czech Republic, containabundant anhydrous spinel lherzolite xenoliths that providean exceptionally continuous sampling of the upper two-thirdsof central European lithospheric mantle. The xenoliths yielda range of two-pyroxene equilibration temperatures from 680°Cto 1070°C, and are estimated to originate from depths of32–70 km, based on a tectonothermal model for basalticunderplating associated with Neogene rifting. The sub-Kozákovmantle is layered, consisting of an equigranular upper layer(32–43 km), a protogranular intermediate layer that containsspinel–pyroxene symplectites after garnet (43–67km), and an equigranular lower layer (67–70 km). Negativecorrelations of wt % TiO2, Al2O3, and CaO with MgO and clinopyroxenemode with Cr-number in the lherzolites record the effects ofpartial fusion and melt extraction; Y and Yb contents of clinopyroxeneand the Cr-number in spinel indicate 5 to 15% partial melting.Subsequent metasomatism of a depleted lherzolite protolith,probably by a silicate melt, produced enrichments in the largeion lithophile elements, light rare earth elements and highfield strength elements, and positive anomalies in primitivemantle normalized trace element patterns for P, Zr, and Hf.Although there are slight geochemical discontinuities at theboundaries between the three textural layers of mantle, theretends to be an overall decrease in the degree of depletion withdepth, accompanied by a decrease in the magnitude of metasomatism.Clinopyroxene separates from the intermediate protogranularlayer and the lower equigranular layer yield 143Nd/144Nd valuesof 0·51287–0·51307 (Nd = +4·6 to+8·4) and 87Sr/86Sr values of 0·70328–0·70339.Such values are intermediate with respect to the Nd–Srisotopic array defined by anhydrous spinel peridotite xenolithsfrom central Europe and are similar to those associated withthe present-day low-velocity anomaly in the upper mantle beneathEurope. The geochemical characteristics of the central Europeanlithospheric mantle reflect a complex evolution related to Devonianto Early Carboniferous plate convergence, accretion, and crustalthickening, Late Carboniferous to Permian extension and gravitationalcollapse, and Neogene rifting, lithospheric thinning, and magmatism. KEY WORDS: xenoliths; lithospheric mantle; REE–LILE–HFSE; Sr–Nd isotopes; Bohemian Massif  相似文献   

11.
A suite of mainly spinel peridotite and subordinate pyroxenite xenoliths and megacrysts were studied in detail, enabling us to characterize upper mantle conditions and processes beneath the modern North American–Eurasian continental plate boundary. The samples were collected from 37-Ma-old basanites cropping out in the Main Collision Belt of the Chersky Range, Yakutia Republic (Russian Far East). The spinel lherzolites reflect a mantle sequence, equilibrated at temperatures of 890–1,025 °C at pressures of 1.1–2 GPa, with melt extraction estimated to be around 2–6 %. The spinel harzburgites are characterized by lower P–T equilibration conditions and estimated melt extraction up to 12 %. Minor cryptic metasomatic processes are recorded in the clinopyroxene trace elements, revealing that percolating hydrous fluid-rich melts and basaltic melts affected the peridotites. One of the lherzolites preserves a unique melt droplet with primary dolomite in perfect phase contact with Na-rich aluminosilicate glass and sodalite. On the basis of the well-constrained P–T frame of the xenolith suite, as well as the rigorously documented melt extraction and metasomatic history of this upper mantle section, we discuss how a carbonated silicate melt infiltrated the lherzolite at depth and differentiated into an immiscible carbonate and silicate liquid shortly before the xenolith was transported to the surface by the host basalt. Decreasing temperatures triggered crystallization of primary dolomite from the carbonate melt fraction and sodalite as well as quenched glass from the Na-rich aluminosilicate melt fraction. Rapid entrainment and transport to the Earth’s surface prevented decarbonatization processes as well as reaction phenomena with the host lherzolite, preserving this exceptional snapshot of upper mantle carbonatization and liquid immiscibility.  相似文献   

12.
 Lherzolite xenoliths in Miocene to Pleistocene basalts from five sites in the Hamar-Daban range in southern Siberia provide sampling of the mantle close to the axis of the Baikal rift. These anhydrous spinel lherzolites commonly have foliated fabrics and spongy rims around clinopyroxene, and many contain accessory feldspar. The feldspar occurs in reaction zones adjacent to spinel and orthopyroxene (where it appears to have been formed by the reaction: spl+opx+cpx+fluid →fs+ol) and less commonly as thin, irregular veins. The feldspars have variable compositions but are generally alkali-rich; their K2O content ranges from 0.3 to 11.2% and is much higher than in plagioclase from orogenic lherzolites (usually <0.1% K2O). The temperature range for the Hamar-Daban xenolith suite (950–1010° C) is more restricted than for spinel peridotite xenoliths from other occurrences in the Baikal area. The feldspar-bearing lherzolites yield equilibration temperatures similar to or slightly lower than feldspar-free ones. The majority of the Hamar-Daban lherzolites are fertile and clinopyroxene-rich, as for most other occurrences in the Baikal region. Trace element compositions of selected xenoliths and their clinopyroxenes were determined by ICP-MS, INAA and proton microprobe. Feldspar-bearing xenoliths are enriched in alkalies indicating that feldspar formation is associated with addition of material and is not simply due to isochemical phase changes. Most xenoliths and their clinopyroxenes studied are depleted in light REE and have contents of Sr, Zr and Y common for fertile or moderately depleted mantle peridotites. Few are moderately enriched in LREE, Sr, Th and U. Sr-Nd isotope compositions of clinopyroxenes indicate long-term depletion in incompatible elements similar to unmetasomatised xenoliths from other occurrences south and east of Lake Baikal. The formation of feldspar and of spongy aggregates after clinopyroxene, and the enrichment in alkalies appear to be recent phenomena related to infiltration of an alkali-rich, H2O-poor fluid into spinel peridotites. Received: 20 March 1995 / Accepted: 26 June 1995  相似文献   

13.
Water partitioning between mantle minerals from peridotite xenoliths   总被引：1，自引：1，他引：1  
The speciation and amount of water dissolved in nominally anhydrous silicates comprising eight different mantle xenoliths has been quantified using synchrotron micro-FTIR spectroscopy. Samples studied are from six geographic localities and represent a cross-section of the major upper mantle lithologies from a variety of tectonic settings. Clinopyroxene contains between 342 and 413 ppm H2O. Orthopyroxene, olivine and garnet contain 169–201, 3–54 and 0 to <3 ppm H2O, respectively. Pyroxenes water contents and the distribution of water between ortho- and clinopyroxene is identical regardless of sample mineralogy (D watercpx/opx = 2.1 ± 0.1). The total water contents of each xenolith are remarkably similar (113 ± 14 ppm H2O). High-resolution spectroscopic traverses show that the concentration and speciation of hydrous defects dissolved in each phase are spatially homogeneous within individual crystals and identical in different crystals interspersed throughout the xenolith. These results suggest that the amount of water dissolved in the silicate phases is in partial equilibrium with the transporting melt. Other features indicate that xenoliths have also preserved OH signatures of equilibrium with the mantle source region: Hydroxyl stretching modes in clinopyroxene show that garnet lherzolites re-equilibrated under more reducing conditions than spinel lherzolites. The distribution of water between pyroxenes and olivine differs according to xenolith mineralogy. The distribution of water between clinopyroxene and olivine from garnet peridotites (D watercpx/oliv(gnt) = 22.2 ± 24.1) is a factor of four greater than mineral pairs from spinel-bearing xenoliths (D watercpx/oliv(sp) = 88.1 ± 47.8). Such an increase in olivine water contents at the spinel to garnet transition is likely a global phenomenon and this discontinuity could lead to a reduction of the upper mantle viscosity by 0.2–0.7 log units and a reduction of its electrical resistivity by a factor of 0.5–0.8 log units.  相似文献   

14.
At the San Luis Potosí (SLP) volcanic field (Central Mexico), Quaternary basanites and tuff breccias have sampled a suite of ultramafic xenoliths, predominately spinel lherzolites, spinel-olivine websterites, spinel pyroxenites, and hornblende-rich pyroxenites. Spinel lherzolites from the La Ventura maars have protogranular to equigranular textures, those from the Santo Domingo maars are strongly sheared. Both spinel-lherzolite types show similar whole-rock major and trace-element abundances. They are fertile to slightly depleted with mineralogical and geochemical heterogeneities induced by partial melting processes. Pyroxenites with either magmatic or metamorphic textures are high-pressure cumulates. Hornblende-rich pyroxenites are genetically linked to the host basanites. Most of the protogranular spinel lherzolites contain veinlets of glass along grain boundaries. These glasses are chemically homogeneous and have trachybasaltic to trachyandesitic compositions. Mg- and Fe2+-partitioning between olivine and glass suggests chemical equilibrium between the melts represented by the glasses and the spinel-lherzolite mineral assemblage at about 1,000°C and 10 to 15 kbar. The melts are interpreted to be of upper mantle origin. They may have been formed by in-situ partial melting in the presence of volatiles or represent percolating melts chemically buffered by the spinel-lherzolite mineral assemblage at uppermost mantle conditions. Mineral chemistry in all rock types of the whole xenolith suite reveals distinct disequilibrium features reflecting partial re-equilibration stages towards lower temperatures estimated to be from 1,050°C to 850°C at 9 to 15 kbar. The presence of similar zoning and exsolution features mainly documented in pyroxenes along with similar maximum and minimum temperatures requires all sampled xenoliths to have undergone the same temperature regime within the upper mantle. The sheared spinel lherzolites from the Sto. Domingo field are interpreted as formerly protogranular material which was sheared during uplift and cooling. The estimated mantle temperatures are higher than those predicted by low heat-flow measurements at the SLP fild, indicating that surface heat flow has not equilibrated to elevated temperatures at depth. This strongly supports a young perturbation event beneath the SLP area and connects the onset of uplift and cooling of the SLP-mantle segment with the back-arc extensional regime of the Quaternary volcanic cycle of the Transmexican Volcanic Belt.  相似文献   

15.
Our knowledge of the lithosphere beneath the Carpathian–Pannonian Region (CPR) has been greatly improved through petrologic, geochemical and isotopic studies of upper mantle xenoliths hosted by Neogene–Quaternary alkali basalts. These basalts occur at the edge of the Intra-Carpathian Basin System (Styrian Basin, Nógrád-Gömör and Eastern Transylvanian Basin) and its central portion (Little Hungarian Plain, Bakony-Balaton Highland).The xenoliths are mostly spinel lherzolites, accompanied by subordinate pyroxenites, websterites, wehrlites, harzburgites and dunites. The peridotites represent residual mantle material showing textural and geochemical evidence for a complex history of melting and recrystallization, irrespective of location within the region. The lithospheric mantle is more deformed in the center of the studied area than towards the edges. The deformation may be attributed to a combination of extension and asthenospheric upwelling in the late Tertiary, which strongly affected the central part of CPR subcontinental lithosphere.The peridotite xenoliths studied show bulk compositions in the following range: 35–48 wt.% MgO, 0.5–4.0 wt.% CaO and 0.2–4.5 wt.% Al2O3 with no significant differences in regard to their geographical location. On the other hand, mineral compositions, particularly of clinopyroxene, vary according to xenolith texture. Clinopyroxenes from less deformed xenoliths show higher contents of ‘basaltic’ major elements compared to the more deformed xenoliths. However, clinopyroxenes in more deformed xenoliths are relatively enriched in strongly incompatible trace elements such as light rare earth elements (LREE).Modal metasomatic products occur as both hydrous phases, including pargasitic and kearsutitic amphiboles and minor phlogopitic micas, and anhydrous phases — mostly clinopyroxene and orthopyroxene. Vein material is dominated by the two latter phases but may also include amphibole. Amphibole mostly occurs as interstitial phases, however, and is more common than phlogopite. Most metasomatized peridotites show chemical and (sometimes) textural evidence for re-equilibration between metasomatic and non-metasomatic phases. However, amphiboles in pyroxenites are sometimes enriched in K, Fe and LREE. The presence of partially crystallized melt pockets (related to amphiboles and clinopyroxenes) in both peridotites and pyroxenites is an indication of decompression melting and, rarely, incipient partial melting triggered by migrating hydrous melts or fluids. Metasomatic contaminants may be ascribed to contemporaneous subduction beneath the Carpathian–Pannonian Region between the Eocene and Miocene.Sulfide inclusions are more abundant in protogranular and porphyroclastic xenoliths relative to equigranular types. In mantle lithologies, sulfide bleb compositions vary between pentlandite and pyrrhotite correlating with the chemistry and texture of the host xenoliths. While sulfides in peridotites are relatively rich in Ni, those in clinopyroxene-rich xenoliths are notably Fe-rich.  相似文献   

16.
Mafic and ultramafic xenoliths in a basaltic cone at The Anakies in south-eastern Australia are geochemically equivalent to continental basaltic magmas and cumulates. The xenolith microstructures range from recognizably meta-igneous for intrusive rocks to granoblastic for garnet pyroxenites. Contact relationships between different rock types within some xenoliths suggest a complex petrogenesis of multiple intrusive, metamorphic and metasomatic events at the crust/mantle boundary during the evolution of south-eastern Australia. Unaltered spinel lher-zolite, typical of the uppermost eastern Australian mantle, is interleaved with or veined by the metamorphosed intrusive rocks of basaltic composition. Geothermobarometry calculations by a variety of methods show a concordance of equilibration temperatures ranging from 880°C to 980°C and pressures of 12 to 18 kbar (1200-1800 mPa). These physical conditions span the gabbro to granulite to eclogite transition boundaries. The water-vapour pressure during equilibration is estimated to be about 0.5% of the load pressure, using amphibole breakdown data. Large fluid inclusions of pure CO2 are abundant in the mineral phases in the xenoliths, and it is suggested that flux of CO2 from the mantle has been an important heat source and fluid medium during metamorphism of the mafic and ultramafic protoliths at the lower crust/upper mantle boundary. The calculated pressures and temperatures suggest that the south-eastern Australian crust has sustained a high geothermal gradient. In addition, the nature of the mineral assemblages and the contact relationships of granulitic rock with spinel lherzolite, characteristic of mantle material, suggest that the Moho is not a discrete feature in this region, but is represented by a transition zone approximately 20 km thick. These inferences are in agreement with geophysical data (including seismic, heat-flow and electrical resistivity data) determined for south-eastern Australia. Underplating at the crust/mantle boundary by continental basaltic magmas may be an important alternative or additional mechanism to the conventional andesite model for crustal accretion.  相似文献   

17.
The Mesozoic lithospheric mantle beneath the North China craton remains poorly constrained relative to its Palaeozoic and Cenozoic counterparts due to a lack of mantle xenoliths in volcanic rocks. Available data show that the Mesozoic lithospheric mantle was distinctive in terms of its major, trace element, and isotopic compositions. The recent discovery of mantle peridotitic xenoliths in Late Cretaceous mafic rocks in the Jiaodong region provides an opportunity to further quantify the nature and secular evolution of the Mesozoic lithospheric mantle beneath the region. These peridotitic xenoliths are all spinel-facies nodules and two groups, high-Mg# and low-Mg# types, can be distinguished based on textural and mineralogical features. High-Mg# peridotites have inequigranular textures, high Mg# (up to 92.2) in olivines, and high Cr# (up to 55) in spinels. Clinopyroxenes in the high-Mg# peridotites are generally LREE-enriched ((La/Yb)N>1) with variable REE concentrations, and have enriched Sr–Nd isotopic compositions (87Sr/86Sr = 0.7046–0.7087; 143Nd/144Nd = 0.5121–0.5126). We suggest that the high-Mg# peridotites are fragments of the Archaean and/or Proterozoic lithospheric mantle that underwent extensive interaction with both carbonatitic and silicate melts prior to or during Mesozoic time. The low-Mg# peridotites are equigranular, are typified by low Mg# ( < 90) in olivines, and by low Cr# ( < 12) in spinels. Clinopyroxenes from low-Mg# peridotites have low REE abundances (ΣREE = 12 ppm), LREE-depleted REE patterns ((La/Yb)N < 1), and depleted Sr–Nd isotopic features, in contrast to the high-Mg# peridotites. These geochemical characteristics suggest that the low-Mg# peridotites represent samples from the newly accreted lithospheric mantle. Combined with the data of mantle xenoliths from the Junan and Daxizhuang areas, a highly heterogeneous, secular evolution of the lithosphere is inferred for the region in Late Cretaceous time.  相似文献   

18.
Magmatic systems of large continental igneous provinces   总被引：1，自引：1，他引：0  
Large igneous provinces (LIPs) formed by mantle superplume events have irreversibly changed their composition in the geological evolution of the Earth from high-Mg melts (during Archean and early Paleoproterozoic) to Phanerozoic-type geochemically enriched Fe-Ti basalts and picrites at 2.3 Ga. We propose that this upheaval could be related to the change in the source and nature of the mantle superplumes of different generations. The first generation plumes were derived from the depleted mantle, whereas the second generation (thermochemical) originated from the core-mantle boundary (CMB). This study mainly focuses on the second (Phanerozoic) type of LIPs, as exemplified by the mid-Paleoproterozoic Jatulian–Ludicovian LIP in the Fennoscandian Shield, the Permian–Triassic Siberian LIP, and the late Cenozoic flood basalts of Syria. The latter LIP contains mantle xenoliths represented by green and black series. These xenoliths are fragments of cooled upper margins of the mantle plume heads, above zones of adiabatic melting, and provide information about composition of the plume material and processes in the plume head. Based on the previous studies on the composition of the mantle xenoliths in within-plate basalts around the world, it is inferred that the heads of the mantle (thermochemical) plumes are made up of moderately depleted spinel peridotites (mainly lherzolites) and geochemically-enriched intergranular fluid/melt. Further, it is presumed that the plume heads intrude the mafic lower crust and reach up to the bottom of the upper crust at depths ～20 km. The generation of two major types of mantle-derived magmas (alkali and tholeiitic basalts) was previously attributed to the processes related to different PT-parameters in the adiabatic melting zone whereas this study relates to the fluid regime in the plume heads. It is also suggested that a newly-formed melt can occur on different sides of a critical plane of silica undersaturation and can acquire either alkalic or tholeiitic composition depending on the concentration and composition of the fluids. The presence of melt-pockets in the peridotite matrix indicates fluid migration to the rocks of cooled upper margin of the plume head from the lower portion. This process causes secondary melting in this zone and the generation of melts of the black series and differentiated trachytic magmas.  相似文献   

19.
Quaternary basalts in the Cerro del Fraile area contain two types of mantle xenoliths; coarse-grained (2–5 mm) C-type spinel harzburgites and lherzolites, and fine-grained (0.5–2 mm) intensely metasomatized F-type spinel lherzolites. C-type xenoliths have high Mg in olivine (Fo = 90–91) and a range in Cr# [Cr/ (Cr + Al) = 0.17–0.34] in spinel. Two C-type samples contain websterite veinlets and solidified patches of melt that is now composed of minute quenched grains of plagioclase + Cr-spinel + clinopyroxene + olivine. These patches of quenched melts are formed by decompression melting of pargasitic amphibole. High Ti contents and common occurrence of relic Cr-spinel in the quenched melts indicate that the amphibole is formed from spinel by interaction with the Ti-rich parental magma of the websterite veinlets. The fO2 values of these two C-type xenoliths range from ΔFMQ −0.2 to −0.4, which is consistent with their metasomatism by an asthenospheric mantle-derived melt. The rest of the C-type samples are free of “melt,” but show cryptic metasomatism by slab-derived aqueous fluids, which produced high concentrations of fluid-mobile elements in clinopyroxenes, and higher fO2 ranging from ΔFMQ +0.1 to +0.3. F-type lherzolites are intensely metasomatized to form spinel with low Cr# (∼0.13) and silicate minerals with low MgO, olivine (Fo = ∼84), orthpyroxene [Mg# = Mg/(Mg + ΣFe) = ∼0.86] and clinopyroxene (Mg# = ∼0.88). Patches of “melt” are common in all F-type samples and their compositions are similar to pargasitic amphibole with low TiO2 (<0.56 wt%), Cr2O3 (<0.55 wt%) and MgO (<16.3 wt%). Low Mg# values of silicate minerals, including the amphibole, suggest that the metasomatic agent is most likely a slab melt. This is supported by high ratios of Sr/Y and light rare earth elements (REE)/heavy REE in clinopyroxenes. F-type xenoliths show relatively low fO2 (ΔFMQ −0.9 to −1.1) compared to C-type xenoliths and this is explained by the fusion of organic-rich sediments overlying the slab during the slab melt. Trench-fill sediments in the area are high in organic matter. The fusion of such wet sediments likely produced CH4-rich fluids and reduced melts that mixed with the slab melt. High U and Th in bulk rocks and clinopyroxene in F-type xenoliths support the proposed interpretation.  相似文献   

20.
An alkali basalt near Glen Innes, northeastern New South Wales, contains a suite of Cr-diopside group ultramafic xenoliths which includes some spinel peridotites but which is dominated by a diverse spinel pyroxenite assemblage. Pyroxenite xenoliths range from subcalcic clinopyroxenites (composed largely of unmixed prismatic subcalcic clinopyroxene megacrystals and lesser orthopyroxene megacrystals) to equant mosaic textured websterites (orthopyroxene and Ca-rich clinopyroxene ± spinel). Rare orthopyroxenite xenoliths also occur. The pyroxenite xenoliths are characterised by high 100Mg/(Mg + Fe2+) ratios (M˜ 90) and low concentrations of Ti, K, P, La, Ce and Zr. The websterites are mineralogically and chemically similar to many spinel pyroxenites occurring as layers or dykes in peridotite massifs such as those at Ronda in southern Spain and at Ariège (French Pyrénées). T / P estimates indicate crystallization temperatures of 1250–1350 °C for subcalcic clinopyroxene-orthopyroxene megacrystal pairs and 900–1000 °C for the equilibrated mosaic textured websterites and associated peridotites at pressures of 9–13 kbar. Subcalcic clinopyroxene megacrystals, websterites and orthopyroxenites have LREE-depleted chondrite-normalised REE abundances with (La/Yb)CN < 1 and their convex-upwards REE patterns are typical of subcalcic clinopyroxene-dominated cumulates. The pyroxenites are not residua from partially melted pyroxenite layers or dykes in mantle peridotites nor are they completely crystallized protobasaltic or protopicritic magmas. They are interpreted as high-pressure crystal segregations from basaltic magmas (probably mildly alkaline or transitional) flowing within narrow mantle conduits (the flow crystallization model of Irving, 1980). The parental magma(s) was Ti-poor (0.6–0.7% TiO2) and relatively Mg-rich (M˜ 74 − 70). Pyroxenite genesis was a two-stage process involving crystallization of tschermakitic subcalcic clinopyroxenes and orthopyroxenes  ±spinel as liquidus or near-liquidus phases at 1250–1350 °C and 9–13 kbar to yield “primary” subcalcic clinopyroxenites which then re-equilibrated at 900–1000 °C and similar pressures to produce the mosaic textured “secondary” websterites. The pyroxenites show a wide range of 143Nd/144Nd and 87Sr/86Sr values (0.513298–0.512473 and 0.702689–0.704659, respectively). Their isotopic ratios appear to have been variably modified by exchange with adjacent mantle peridotites or migrating basaltic melts. Received: 11 December 1995 / Accepted: 3 December 1996  相似文献   

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