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1.
Volcán San Pedro in the Andean Southern Volcanic Zone(SVZ) Chile, comprises Holocene basaltic to dacitic lavas withtrace element and strontium isotope ratios more variable thanthose of most Pleistocene lavas of the underlying Tatara–SanPedro complex. Older Holocene activity built a composite coneof basaltic andesitic and silicic andesitic lavas with traceelement ratios distinct from those of younger lavas. Collapseof the ancestral volcano triggered the Younger Holocene eruptivephase including a sequence of lava flows zoned from high-K calc-alkalinehornblende–biotite dacite to two-pyroxene andesite. Notably,hornblende–phlogopite gabbroic xenoliths in the daciticlava have relatively low 87Sr/86Sr ratios identical to theirhost, whereas abundant quenched basaltic inclusions are moreradiogenic than any silicic lava. The latest volcanism rebuiltthe modern 3621 m high summit cone from basaltic andesite thatis also more radiogenic than the dacitic lavas. We propose thefollowing model for the zoned magma: (1) generation of hornblende–biotitedacite by dehydration partial melting of phlogopite-bearingrock similar to the gabbroic xenoliths; (2) forceful intrusionof basaltic magma into the dacite, producing quenched basalticinclusions and dispersion of olivine and plagioclase xenocryststhroughout the dacite; (3) cooling and crystallization–differentiationof the basalt to basaltic andesite; (4) mixing of the basalticandesite with dacite to form a small volume of two-pyroxenehybrid andesite. The modern volcano comprises basaltic andesitethat developed independently from the zoned magma reservoir.Evolution of dacitic and andesitic magma during the Holoceneand over the past 350 kyr reflects the intrusion of multiplemafic magmas that on occasion partially melted or assimilatedhydrous gabbro within the shallow crust. The chemical and isotopiczoning of Holocene magma at Volcán San Pedro is paralleledby that of historically erupted magma at neighboring VolcánQuizapu. Consequently, the role of young, unradiogenic hydrousgabbro in generating dacite and contaminating basalt may beunderappreciated in the SVZ. KEY WORDS: Andes; dacite; gabbro; Holocene; strontium isotopes  相似文献   

2.
Summary Mantle-derived xenoliths from Baarley in the Quaternary West Eifel volcanic field contain six distinct varieties of glass in veins, selvages and pools. 1) Silica-undersaturated glass rich in zoned clinopyroxene microlites that forms jackets around and veins within the xenoliths. This glass is compositionally similar to groundmass glass in the host basanite. 2) Silica-undersaturated alkaline glass that contains microlites of Cr-diopside, olivine and spinel associated with amphibole in peridotites. This glass locally contains corroded primary spinel and phlogopite. 3) Silica-undersaturated glass associated with diopside, spinel ± olivine and rh?nite microlites in partly to completely broken down amphibole grains in clinopyroxenites. 4) Silica-undersaturated to silica-saturated, potassic glass in microlite-rich fringes around phlogopite grains in peridotite. 5) Silica-undersaturated potassic glass in glimmerite xenoliths. 6) Silica-rich glass around partly dissolved orthopyroxene crystals in peridotites. Geothermometry of orthopyroxene–clinopyroxene pairs (P = 1.5 GPa) gives temperatures of ∼ 850 °C for unveined xenoliths to 950–1020 °C for veined xenoliths. Clinopyroxene – melt thermobarometry shows that Cr-diopside – type 2 glass pairs in harzburgite formed at 1.4 to 1.1 GPa and ∼ 1250 °C whereas Cr-diopside – type 2 glass pairs in wehrlite formed at 0.9 to 0.7 GPa and 1120–1200 °C. This bimodal distribution in pressure and temperature suggests that harzburgite xenoliths may have been entrained at greater depth than wehrlite xenoliths. Glass in the Baarley xenoliths has three different origins: infiltration of an early host melt different in composition from the erupted host basanite; partial melting of amphibole; reaction of either of these melts with xenolith minerals. The composition of type 1 glass suggests that jackets are accumulations of relatively evolved host magma. Mass balance modelling of the type 2 glass and its microlites indicates that it results from breakdown of disseminated amphibole and reaction of the melt with the surrounding xenolith minerals. Type 3 glass in clinopyroxenite xenoliths is the result of breakdown of amphibole at low pressure. Type 4 and 5 glass formed by reaction between phlogopite and type 2 melt or jacket melt. Type 6 glass associated with orthopyroxene is due to the incongruent dissolution of orthopyroxene by any of the above mentioned melts. Compositional gradients in xenolith olivine adjacent to type 2 glass pools and jacket glass can be modelled as Fe–Mg interdiffusion profiles that indicate melt – olivine contact times between 0.5 and 58 days. Together with the clinopyroxene – melt thermobarometry calculations these data suggest that the glass (melt) formed over a short time due to decompression melting of amphibole and infiltration of evolved host melt. None of the glass in these xenoliths can be directly related to metasomatism or any other process that occurred insitu in the mantle. Received November 23, 1999; revised version accepted September 5, 2001  相似文献   

3.
  1. Xenoliths of ultrabasic, ultramafic, gabbroic or syenitic type occur in Teneriffe: dunites and clino-pyroxenites in the old alkalic basalt formations of Teno and Anaga peninsulas; gabbroic xenoliths in the Pedro Gil region; nepheline-syenite xenoliths in the Las Canadas and Vilaflor regions where intermediate and phonolitic lavas are abundant; ultramafic, clino-pyroxenite and syenitic xenoliths in the Anaga peninsula where there are many intrusions of nepheline-syenite and phonolitic syenite. Several xenoliths show signs of cataclasis, recrystallisation or reaction of their minerals with the host liquids.
  2. The ultrabasic, ultramafic and anorthoclase-rich xenoliths appear to be of cumulus origin, subtracted from basic to intermediate alkalic liquids. Major cumulus phases are: magnesium-rich olivine, sub-silicic, aluminous pyroxene, titanomagnetite, sub-silicic potassic kaersutite, and anorthoclase. It is suggested that the xenoliths formed at depths between 11 km and 30 km, largely under wet conditions that helped suppress formation of cumulus plagioclase.
  3. The subtraction of kaersutite from liquids of intermediate composition is thought to be a means of producing the gap in silica content between the Teneriffe trachybasalts and the more siliceous trachyphonolites and phonolites. It is also suggested that the subtraction of kaersutite and anorthoclase would considerably deplete residual liquids in alumina whilst enriching then in soda and this might be the means of producing peralkaline liquids.
  4. The presence of the xenoliths supports the geophysical data that indicated that Teneriffe has a sub-crustal structure of plutonic rocks. Correlation of the Teneriffe plutonic xenoliths with exposed plutonic basement rocks from other Canary Islands, which are believed to have similar sub-crustal structures, is considered necessary.
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4.
St. Kitts lies in the northern Lesser Antilles, a subduction-related intraoceanic volcanic arc known for its magmatic diversity and unusually abundant cognate xenoliths. We combine the geochemistry of xenoliths, melt inclusions and lavas with high pressure–temperature experiments to explore magma differentiation processes beneath St. Kitts. Lavas range from basalt to rhyolite, with predominant andesites and basaltic andesites. Xenoliths, dominated by calcic plagioclase and amphibole, typically in reaction relationship with pyroxenes and olivine, can be divided into plutonic and cumulate varieties based on mineral textures and compositions. Cumulate varieties, formed primarily by the accumulation of liquidus phases, comprise ensembles that represent instantaneous solid compositions from one or more magma batches; plutonic varieties have mineralogy and textures consistent with protracted solidification of magmatic mush. Mineral chemistry in lavas and xenoliths is subtly different. For example, plagioclase with unusually high anorthite content (An≤100) occurs in some plutonic xenoliths, whereas the most calcic plagioclase in cumulate xenoliths and lavas are An97 and An95, respectively. Fluid-saturated, equilibrium crystallisation experiments were performed on a St. Kitts basaltic andesite, with three different fluid compositions (XH2O = 1.0, 0.66 and 0.33) at 2.4 kbar, 950–1025 °C, and fO2 = NNO ? 0.6 to NNO + 1.2 log units. Experiments reproduce lava liquid lines of descent and many xenolith assemblages, but fail to match xenolith and lava phenocryst mineral compositions, notably the very An-rich plagioclase. The strong positive correlation between experimentally determined plagioclase-melt KdCa–Na and dissolved H2O in the melt, together with the occurrence of Al-rich mafic lavas, suggests that parental magmas were water-rich (> 9 wt% H2O) basaltic andesites that crystallised over a wide pressure range (1.5–6 kbar). Comparison of experimental and natural (lava, xenolith) mafic mineral composition reveals that whereas olivine in lavas is predominantly primocrysts precipitated at low-pressure, pyroxenes and spinel are predominantly xenocrysts formed by disaggregation of plutonic mushes. Overall, St. Kitts xenoliths and lavas testify to mid-crustal differentiation of low-MgO basalt and basaltic andesite magmas within a trans-crustal, magmatic mush system. Lower crustal ultramafic cumulates that relate parental low-MgO basalts to primary, mantle -derived melts are absent on St. Kitts.  相似文献   

5.
In order to shed light on upper crustal differentiation of mantle-derived basaltic magmas in a subduction zone setting, we have determined the mineral chemistry and oxygen and hydrogen isotope composition of individual cumulus minerals in plutonic blocks from St. Vincent, Lesser Antilles. Plutonic rock types display great variation in mineralogy, from olivine–gabbros to troctolites and hornblendites, with a corresponding variety of cumulate textures. Mineral compositions differ from those in erupted basaltic lavas from St. Vincent and in published high-pressure (4–10 kb) experimental run products of a St. Vincent high-Mg basalt in having higher An plagioclase coexisting with lower Fo olivine. The oxygen isotope compositions (δ18O) of cumulus olivine (4.89–5.18‰), plagioclase (5.84–6.28‰), clinopyroxene (5.17–5.47‰) and hornblende (5.48–5.61‰) and hydrogen isotope composition of hornblende (δD = −35.5 to −49.9‰) are all consistent with closed system magmatic differentiation of a mantle-derived basaltic melt. We employed a number of modelling exercises to constrain the origin of the chemical and isotopic compositions reported. δ18OOlivine is up to 0.2‰ higher than modelled values for closed system fractional crystallisation of a primary melt. We attribute this to isotopic disequilibria between cumulus minerals crystallising at different temperatures, with equilibration retarded by slow oxygen diffusion in olivine during prolonged crustal storage. We used melt inclusion and plagioclase compositions to determine parental magmatic water contents (water saturated, 4.6 ± 0.5 wt% H2O) and crystallisation pressures (173 ± 50 MPa). Applying these values to previously reported basaltic and basaltic andesite lava compositions, we can reproduce the cumulus plagioclase and olivine compositions and their associated trend. We conclude that differentiation of primitive hydrous basalts on St. Vincent involves crystallisation of olivine and Cr-rich spinel at depth within the crust, lowering MgO and Cr2O3 and raising Al2O3 and CaO of residual melt due to suppression of plagioclase. Low density, hydrous basaltic and basaltic andesite melts then ascend rapidly through the crust, stalling at shallow depth upon water saturation where crystallisation of the chemically distinct cumulus phases observed in this study can occur. Deposited crystals armour the shallow magma chamber where oxygen isotope equilibration between minerals is slowly approached, before remobilisation and entrainment by later injections of magma.  相似文献   

6.
DOWNES  H. 《Journal of Petrology》2001,42(1):233-250
The petrology and geochemistry of shallow continental lithosphericmantle (SCLM) can be studied via (1) tectonically emplaced ultramaficmassifs and (2) mantle xenoliths entrained in alkaline magmas.Data from these two separate sources are used to identify processesthat have formed and modified the SCLM. In western and centralEurope where the continental crust consolidated in Phanerozoictimes, both sources of information are available for study.Rock types found in ultramafic massifs in Europe are generallysimilar to those found in ultramafic xenolith suites. The mostfrequent lithology is anhydrous spinel lherzolite, grading towardsharzburgite. Massifs reveal pyroxenite layering, harzburgitebands and cross-cutting mafic and ultramafic dykes. The PhanerozoicEuropean SCLM xenoliths and massifs show broad mineralogicaland chemical similarities to Phanerozoic continental spinelperidotites world-wide. The main process that controls the geochemistryof the SCLM is depletion by removal of basaltic melt. Differencesfrom this norm reflect significantly different processes inthe SCLM, such as interaction with melts and fluids. Such processesprobably gave rise to hornblendite veins and pyroxenite layers,although the latter have also been interpreted as recycled oceaniccrust. Rare earth element data for whole-rock peridotites andtheir constituent clinopyroxenes show a variety of patterns,including light rare earth element (LREE) depletion as a resultof removal of basaltic melt, LREE enrichment caused by metasomatism,and U-shaped REE patterns that are probably due to interactionwith carbonatite melts. Extended mantle-normalized incompatibletrace element patterns for whole rocks show enrichment in Rband Ba in peridotites considered to have been subduction-metasomatized,whereas those considered to be carbonate-metasomatized havestrong negative anomalies in Zr, Nb and Hf. Mantle amphibolesare strongly enriched in LREE when found in veins, but can beLREE depleted if they are interstitial. Radiogenic isotope ratiosfor xenoliths and massifs largely overlap, although the xenolithsshow a significant clustering around a ‘plume-component’identical to the Neogene alkaline magmatism of Europe. Thiscomponent is lacking in the massifs, most of which were emplacedinto the crust before the onset of Neogene plume activity. Infiltrationof carbonatite melts is observed petrographically in some xenolithsand evidenced by low Ti/Eu ratios in bulk rocks, but is veryrare. The effect of passage of hydrous fluids from subductingslabs is also seen in some suites and massifs, being exhibitedmainly as unusual Sr and Pb isotope ratios, although enrichmentin K, Rb and Ba, and the presence of modal phlogopite, may alsopoint to subduction-metasomatism. KEY WORDS: peridotites; xenoliths; orogenic massifs; Europe  相似文献   

7.
A rare composite xenolith and abundant cumulative pyroxenites obtained from the Mesozoic Fangcheng basalts on the eastern North China Craton record a complex history of melt percolation and circulation in the subcontinental lithospheric mantle. The composite xenolith has a dunite core and an olivine clinopyroxenite rim. The dunite is of cumulative origin and has a granular recrystallized texture and extremely low Mg# [100 Mg/(Mg + Fe) = 81–82] contents in olivines. The olivine clinopyroxenite contains larger clinopyroxene and/or orthopyroxene with a few fine-grained olivine and tiny phlogopite, feldspar, and/or carbonate minerals interstitial to clinopyroxene. The clinopyroxene has low Mg# (83–85). Compositional similarity between dunitic olivine and pyroxenitic one indicates a sequential crystallization of dunite and pyroxenite from a precursor melt. Pyroxenite xenoliths include olivine websterites and clinopyroxenites, both are of cumulative origin. Estimation of the melt from major oxides in olivines and REE concentrations in clinopyroxenes in these composite and pyroxenite xenoliths suggests a derivation from subducted crustal materials, consistent with the highly enriched EMII-like Sr and Nd isotopic ratios observed in the pyroxenites. Occurrence of phlogopite, feldspar and carbonate minerals in some xenoliths requires the melt rich in alkalis (K, Na), silica and volatiles (water and CO2) at the latest stage as well, similar to highly silicic and potassic melts. Thus, the occurrence of these composite and pyroxenite xenoliths provides an evidence for voluminous injection of recycled crustal melts into the lithosphere beneath the southeastern North China Craton at the Late Mesozoic, a reason for the rapid lithospheric enrichment in both elemental and isotopic compositions.  相似文献   

8.
The Tunk Lake pluton of coastal Maine, USA is a concentrically zoned granitic body that grades from an outer hypersolvus granite into subsolvus rapakivi granite, and then into subsolvus non-rapakivi granite, with gradational contacts between these zones. The pluton is partially surrounded by a zone of basaltic and gabbroic enclaves, interpreted as quenched magmatic droplets and mushes, respectively, as well as gabbroic xenoliths, all hosted by high-silica granite. The granite is zoned in terms of mineral assemblage, mineral composition, zircon crystallization temperature, and major and trace element concentration, from the present-day rim (interpreted as being closer to the base of the chamber) to the core (interpreted as being closer to the upper portions of the chamber). The ferromagnesian mineral assemblage systematically changes from augite and hornblende with augite cores in the outermost hypersolvus granite to hornblende, to hornblende and biotite, and finally, to biotite only in the subsolvus granite core of the pluton. Sparse fine-grained basaltic enclaves that are most common in the outermost zone of the pluton suggest that basaltic magma was present in the lower portions of the magma chamber at the same time that the upper portions of the magma chamber were occupied by a granitic crystal mush. However, the slight variations in initial Nd isotopic ratio in granites from different zones of the pluton suggest that contamination of the granitic melt by basaltic melt played little role in generating the compositional gradation of the pluton. The zone of basaltic and gabbroic chilled magmatic enclaves, and gabbroic xenoliths, hosted by high-silica granite, that partially surround the pluton is interpreted as mafic layers at the base of the pluton that were disrupted by invading late-stage high-silica magma. These mafic layers are likely to have consisted of basaltic lava layers and basalt that chilled against granitic magma to produce coarse-grained gabbroic mush. Basaltic and gabbroic magmatic enclaves and gabbroic xenoliths are hornblende-bearing, suggesting that their parent melts were relatively hydrous. The water-rich nature of the underplating mafic magmas may have prevented extensive invasion of the granitic magma by these magmas, owing to the much greater viscosity of the granitic magma than the mafic magmas in the temperature range over which magma interaction could have occurred.  相似文献   

9.
Mantle xenoliths in alkaline lavas of the Kerguelen Islandsconsist of: (1) protogranular, Cr-diopside-bearing harzburgite;(2) poikilitic, Mg-augite-bearing harzburgite and cpx-poor lherzolite;(3) dunite that contains clinopyroxene, spinel phlogopite, andrarely amphibole. Trace element data for rocks and mineralsidentify distinctive signatures for the different rock typesand record upper-mantle processes. The harzburgites reflectan initial partial melting event followed by metasomatism bymafic alkaline to carbonatitic melts. The dunites were firstformed by reaction of a harzburgite protolith with tholeiiticto transitional basaltic melts, and subsequently developed metasomaticassemblages of clinopyroxene + phlogopite ± amphiboleby reaction with lamprophyric or carbonatitic melts. We measuredtwo-mineral partition coefficients and calculated mineral–meltpartition coefficients for 27 trace elements. In most samples,calculated budgets indicate that trace elements reside in theconstituent minerals. Clinopyroxene is the major host for REE,Sr, Y, Zr and Th; spinel is important for V and Ti; orthopyroxenefor Ti, Zr, HREE, Y, Sc and V; and olivine for Ni, Co and Sc. KEY WORDS: mantle xenoliths; mantle metasomatism; partition coefficients; Kerguelen Islands; trace elements  相似文献   

10.
An unusual quartz-bearing orthopyroxene-rich websterite xenolithhas been found in an alkali basaltic tuff at Szigliget, Bakony–BalatonHighland Volcanic Field (BBHVF), western Hungary. Ortho- andclinopyroxenes are enriched in light rare earth elements (LREE),middle REE and Ni, and depleted in Nb, Ta, Sr and Ti comparedwith ortho- and clinopyroxenes occurring in either peridotiteor lower crustal granulite xenoliths from the BBHVF. Both ortho-and clinopyroxenes in the xenolith contain primary and secondarysilicate melt inclusions, and needle-shaped or rounded quartzinclusions. The melt inclusions are rich in SiO2 and alkalisand poor in MgO, FeO and CaO. They are strongly enriched inLREE and large ion lithophile elements, and display negativeNb, Ta and Sr anomalies, and slightly positive Pb anomalies.The xenolith is interpreted to represent a fragment of an orthopyroxene-richbody that crystallized in the upper mantle from a hybrid meltthat formed by interaction of mantle peridotite with a quartz-saturatedsilicate melt that was released from a subducted oceanic slab.Although the exact composition of the slab melt cannot be determined,model calculations on major and trace elements suggest involvementof a metasedimentary component. KEY WORDS: quartz; mantle; silicate melt inclusion; SiO2-rich melt; subduction; Carpathian-Pannonian Region  相似文献   

11.
 Mantle xenoliths hosted by the Historic Volcan de San Antonio, La Palma, Canary Islands, fall into two main group. Group I consists of spinel harzburgites, rare spinel lherzolites and spinel dunites, whereas group II comprises spinel wehrlites, amphibole wehrlites, and amphibole clinopyroxenites. We here present data on group I xenoliths, including veined harzburgites and dunites which provide an excellent basis for detailed studies of metasomatic processes. The spinel harzburgite and lherzolite xenoliths have modal ol−opx−cpx ratios and mineral and whole rock major element chemistry similar to those found in Lanzarote and Hierro, and are interpreted as highly refractory, old oceanic lithospheric mantle. Spinel dunites are interpreted as old oceanic peridotite which has been relatively enriched in olivine and clinopyroxene (and highly incompatible elements) through reactions with basaltic Canarian magmas, with relatively high melt/peridotite ratio. Group I xenoliths from La Palma differ from the Hierro and Lanzarote ones by a frequent presence of minor amounts of phlogopite (and amphibole). Metasomatic processes are also reflected in a marked enrichment of strongly incompatible relative to moderately incompatible trace elements, and in a tendency for Fe−Ti enrichment along grain boundaries in some samples. The veins in the veined xenoliths show a gradual change in phase assemblage and composition of each phase, from Fe−Ti-rich amphibole+augite+Fe−Ti-oxides+apatite+basaltic glass, to Ti-poor phlogopite+Cr-diopside±chromite+ Si−Na−K-rich glass+fluid. Complex reaction zones between veins and peridotite include formation of clinopyroxene±olivine+glass at the expense of orthopyroxene in harzburgite, and clinopyroxene+spinel±amphibole±glass at the expense of olivine in dunite. The dramatic change in glass composition from the broadest to the narrowest veins includes increasing SiO2 from 44 to 67 wt%, decreasing TiO2/Al2O3 ratio from >0.24 to about 0.02, and increasing K2O and Na2O from 1.8 to >7.0 wt% and 3.8 to 6.7 wt%, respectively. The petrographic observations supported by petrographic mixing calculations indicate that the most silicic melts in the veined xenoliths formed as the result of reaction between infiltrating basaltic melt and peridotite wall-rock. The highly silicic, alkaline melt may represent an important metasomatic agent. Pervasive metasomatism by highly silicic melts (and possibly fluids unmixed from these) may account for the enriched trace element patterns and frequent presence of phlogopite in the upper mantle under La Palma. Received: 15 January 1996 / Accepted 30 May 1996  相似文献   

12.
Extrusive and intrusive igneous rocks represent different parts of a magmatic system and ultimately provide complementary information about the processes operating beneath volcanoes. To shed light on such processes, we have examined and quantified the textures and mineral compositions of plutonic and cumulate xenoliths and lavas from Bequia, Lesser Antilles arc. Both suites contain assemblages of iddingsitized olivine, plagioclase, clinopyroxene and spinel with rare orthopyroxene and ilmenite. Mineral zoning is widespread, but more protracted in lavas than xenoliths. Plagioclase cores and olivine have high anorthite (An?≤?98) and low forsterite (Fo?≤?84) compositions respectively, implying crystallisation from a hydrous mafic melt that was already fractionated. Xenolith textures range from adcumulate to orthocumulate with variable mineral crystallisation sequences. Textural criteria are used to organize the xenoliths into six groups. Amphibole, notably absent from lavas, is a common feature of xenoliths, together with minor biotite and apatite. Bulk compositions of xenoliths deviate from the liquid line of descent of lavas supporting a cumulate origin with varying degrees of reactive infiltration by evolved hydrous melts, preserved as melt inclusions in xenolith crystals. Volatile saturation pressures in melt inclusions indicate cumulate crystallization over a 162–571 MPa pressure range under conditions of high dissolved water contents (up to 7.8 wt% H2O), consistent with a variety of other thermobarometric estimates. Phase assemblages of xenoliths are consistent with published experimental data on volatile-saturated low-magnesium and high-alumina basalts and basaltic andesite from the Lesser Antilles at pressures of 200–1000 MPa, temperatures of 950–1050 °C and dissolved H2O contents of 4–7 wt%. Once extracted from mid-crustal mushes, residual melts ascend to higher levels and undergo H2O-saturated crystallization in shallow, pre-eruptive reservoirs to form phenocrysts and glomerocrysts. The absence of amphibole from lavas reflects instability at low pressures, whereas its abundance in xenoliths testifies to its importance in mid-crustal differentiation processes. A complex, vertically extensive (6 to at least 21 km depth) magmatic system is inferred beneath Bequia. Xenoliths represent fragments of the mush incorporated into ascending magmas. The widespread occurrence of evolved melts in the mush, but the absence of erupted evolved magmas, in contrast to islands in the northern Lesser Antilles, may reflect the relative immaturity of the Bequia magmatic system.  相似文献   

13.
Residence times of plagioclase crystals in magma reservoirs can be determined by modeling the compositional zoning of trace elements in these crystals. We present a formulation to model diffusion of trace elements in plagioclase paying special attention to certain thermodynamic and kinetic aspects. In particular, we account for the compositional dependence on anorthite content of the chemical potential and diffusion coefficients of trace elements (e.g., Mg), the choice of suitable boundary conditions and potential effects of diffusion in more than one dimension. We show that contrary to intuition, diffusive fluxes of trace elements may be coupled to major element concentration gradients, and ignoring such coupling can lead to incorrect estimates of timescales. We illustrate application of the model using plagioclase crystals from a suite of gabbroic xenoliths from a Holocene dacitic lava flow of Volcán San Pedro (Chilean Andes, 36°S). The inferred timescale for metasomatism of the xenoliths by evolved liquids is on the order of 100 (30 to 148) yr and serves to illustrate how trace element zoning in plagioclase provides a window into timescales of magmatic processes inaccessible by isotopic or other methods.  相似文献   

14.
The Quaternary Tatara–San Pedro volcanic complex (36°S,Chilean Andes) comprises eight or more unconformity-bound volcanicsequences, representing variably preserved erosional remnantsof volcanic centers generated during  相似文献   

15.
Anorthositic rocks compose 35–40% of the Middle Proterozoic(Keweenawan; 1?1 Ga) Duluth Complex—a large, compositemafic body in northeastern Minnesota that was intruded beneatha comagmatic volcanic edifice during the formation of the Midcontinentrift system. Anorthositic rocks, of which six general lithologictypes occur in one area of the complex, are common in an earlyseries of intrusions. They are characterized on a local scale(meters to kilometers) by nonstratiform distribution of rocktypes, variably oriented plagioclase lamination, and compositeintrusive relationships. Variably zoned, subhedral plagioclaseof nearly constant average An (60) makes up 82–98% ofthe anorthositic rocks. Other phases include granular to poikiliticolivine (Fo66–38), poikilitic clinopyrox-ene (En'73–37),subpoikilitic Fe-Ti oxides, and various late-stage and secondaryminerals. Whole-rock compositions of anorthositic rocks are modelled bymass balance to consist of three components: cumulus plagioclase(70–95 wt.%), minor cumulus olivine (0–5%), anda gabbroic postcumulus assemblage (5–27%) representinga trapped liquid. The postcumulus assemblage has textural andcompositional characteristics which are consistent with crystallizationfrom basaltic magma ranging from moderately evolved olivinetholeiite to highly evolved tholeiite (mg=60–25). Sympatheticvariations of mg in plagioclase and in mafic minerals suggestthat cumulus plagioclase, though constant in An, was in approximateequilibrium with the variety of basaltic magma compositionswhich produced the postcumulus assemblages. Standard models of mafic cumulate formation by fractional crystallizationof basaltic magmas in Duluth Complex chambers, although ableto explain the petrogenesis of younger stratiform troctoliticto gabbroic intrusions, are inadequate to account for the field,petrographic, and geochemical characteristics of the anorthositicrocks. Rather, we suggest an origin by multiple intrusions ofplagioclase crystal mushes—basaltic magmas charged withas much as 60% intratelluric plagioclase. The high concentrationsof cumulus plagioclase (70–95%) estimated to compose theanorthositic rocks may reflect expulsion of some of the transportingmagma during emplacement or early postcumulus crystallizationof only plagioclase from evolved hyperfeldspathic magma. Althoughthe evolved compositions of anorthositic rocks require significantfractionation of mafic minerals, geophysical evidence indicatesthat ultramafic rocks are, as exposure implies, rare in theDuluth Complex and implies that plagioclase crystal mushes werederived from deeper staging chambers. This is consistent withinterpretations of olivine habit and plagioclase zoning. Moreover,plagioclase could have been segregated from coprecipitatingmafic phases in such lower crustal chambers because of the buoyancyof plagioclase in basaltic magmas at high pressure. The geochemicaleffects of plagioclase suspension in basaltic magmas are consistentwith observed compositions of cumulus plagioclase in the anorthositicrocks and with the geochemical characteristics of many comagmaticbasalts. The petrogenesis of the anorthositic rocks and theoverall evolution of Keweenawan magmas can be related to thedynamics of intracontinental rift formation.  相似文献   

16.
Seven alkali basalt centers in the southern Canadian Cordilleracontain mantle xenolith suites that comprise spinel Cr-diopsideperidotites, spinel augite-bearing wehrlites and orthopyroxene-poorlherzolites, and minor pyroxenites. The Cr-diopside peridotitesappear to be residues of the extraction of Mg-rich basalts byup to 15% partial melting (median 5–10%) of a pyrolite-likesource in the spinel stability field. The xenoliths are similarto other mantle xenolith suites derived from beneath convergentcontinental margins, but are less depleted, less oxidized, andhave lower spinel mg-number than peridotites found in fore-arcsettings. Their dominant high field strength element depletedcharacter, however, is typical of arc lavas, and may suggestthat fluids or melts circulating through the Canadian Cordilleralithosphere were subduction related. Modeling using MELTS isconsistent with the augite-bearing xenoliths being formed byinteraction between crystallizing alkaline melts and peridotite.Assimilation–fractional crystallization modeling suggeststhat the trace element patterns of liquids in equilibrium withthe augite xenoliths may represent the initial melts that reactedwith the peridotite. Moreover, the compositions of these meltsare similar to those of some glasses observed in the mantlexenoliths. Melt–rock interaction may thus be a viablemechanism for the formation of Si- and alkali-rich glass inperidotites. KEY WORDS: Canadian Cordillera; mantle xenolith; peridotite; wehrlite; melt–rock reaction  相似文献   

17.
Abundant spinel peridotite xenoliths occur in late Cenozoic alkali basaltic rocks in the Sikhote-Alin region at the Pacific margin of the Asian continent. Major- and trace-element compositions of representative peridotite xenolith are documented for four occurrences located in different structural units of the continental margin. In each locality, the majority of xenoliths have distinctive microstructures, modal and chemical compositions that are typical for a given xenolith suite. Significant textural and compositional differences between the four xenolith suites suggest that the upper mantle beneath the Sikhote-Alin consists of distinct domains with contrasting composition. The inferred large-scale mantle heterogeneities may be due to juxtaposition of lithospheric blocks of different provenance during accretion of the Sikhote-Alin to the Asian continent.

Trace-element patterns of the xenoliths and their minerals obtained ICP-MS technique provide evidence of depletion and enrichment events and indicate contrasting behaviour of REE, HFSE and other incompatible trace elements. The HFSE behave non-concordantly, in particular, some xenoliths have highly fractionated Zr/Hf, Ti/Zr, Nb/Ta, La/Nb and U/Th ratios relative to their values in the primitive mantle. The fractionated compositions may be related to the interaction of evolved subduction-related fluids and melts with lithospheric mantle at the Mesozoic-early Cenozoic active continental margin or to metasomatism during later continental rifting.  相似文献   


18.
Cliff S.J. Shaw   《Lithos》1997,40(2-4):243-259
The Coldwell alkaline complex is a large (> 350 km2) gabbro and syenite intrusion on the north shore of Lake Superior. It was emplaced at 1108 Ma during early magmatic activity associated with the formation of the Mid-Continent Rift of North America. The eastern gabbro forms a partial ring dyke on the outer margin of the complex and consists of at least three discrete intrusions. The largest of these is the layered gabbro that comprises a 300 m thick fine- to medium-grained basal unit overlain by up to 1100 m of variably massive to layered gabbroic cumulates which vary from olivine gabbro to anorthosite. Several xenoliths of Archaean metamorphic rocks that range in size from 10's to 100's of meters are present in the central part of the intrusion. Within discrete horizons in the layered gabbro are many centimeter- to meter-scale, gabbroic xenoliths. The main cumulus minerals, in order of crystallization, are plagioclase, olivine and clinopyroxene ± Fe-Ti oxides. Biotite and Fe-Ti-oxide are the dominant intercumulus phases. Orthopyroxene occurs not as a cumulus phase but as peritectic overgrowths on cumulus olivine. A detailed petrographic and mineral chemical study of samples from two stratigraphically controlled traverses through the layered gabbro indicates that the stratigraphy cannot be correlated along the 33 km strike of the ring dyke. Mineral compositions show both normal and reversed fractionation trends. These patterns are interpreted to record at least three separate intrusions of magma into restricted dilatant zones within the ring dyke possibly associated with ongoing caldera collapse. Calculations of parental melt composition using mineral — melt equilibria show that even the most primitive gabbros crystallized from an evolved magma with mg# of 0.42-0.49. The presence of orthopyroxene overgrowths on cumulus olivine suggests rising silica activity in the melt during crystallization and implies a subalkaline parentage for the layered gabbro.  相似文献   

19.
Petrology of Santorini Volcano, Cyclades, Greece   总被引:1,自引:1,他引:1  
The Pliocene to Recent lavas, dyke rocks, and cognate xenolithsof Santorini island group belong to four distinct series, eachof high-alumina basalt-andesite-dacite type. The oldest seriesincludes hornblende dacites and minor basaltic andesites. Theformer contain hornblende-rich cognate xenoliths of basalticcomposition, which consist essentially of crystals ‘floating’in residual acid liquid (glass). The chemical variation of theseries, like that of lavas of volcanic centres north-west ofSantorini, is of ‘calc-alkali’ type. The second and third series consist of a range of lavas frombasalt to rhyodacite. No hydrous mineral occurs as a stablephase. Augite is the phenocrystal pyroxene of basalts; augiteand hypersthene of andesites and dacites. The groundmass pyroxenesof basalts and most andesites are augite and pigeonite, whiledistinctive hornblende xenocryst-bearing andesites of the secondseries, and acid lavas of both second and third, carry augiteand hypersthene in the groundmass. Interstitial glass increasesin proportion from basalts to andesites, and forms a major componentof acid lavas. The second series, like the oldest, lacks absoluteiron enrichment. The third, however, shows weak iron enrichmentof andesitic relative to basaltic compositions. Of the youngest (historic) series, only the acid members (hyalodacites)have been extruded as lavas. The more basic members are representedby non-cumulate xenoliths of basaltic to andesitic compositionwhich, like those of the oldest series, consist of a mesh ofcrystals set in abundant glass. This modern series also displaysfeeble absolute iron enrichment. The compositional range of minerals other than plagioclase isvery limited in the two xenolithic series, but much greaterin the two lava series. Glass compositions are virtually constantwithin individual series. Estimates of temperatures and oxygenfugacities of Fe-Ti oxide mineral equilibration, and deductionsfrom liquid compositional trends indicate that the oldest serieswas characterized by higher fO2, and fH2O, and lower temperaturesthan the three younger, ‘dry’ series. Its silicaenrichment trend appears to have been controlled chiefly byfractionation of silica-poor hornblende, rather than magnetiteas in the younger series. The presence, in all series, of xenolithsof gabbroic cumulates, and the constancy of glass compositionssuggests that each series was generated by the tapping of adifferentiating highalumina basalt magma in a high level magmachamber.  相似文献   

20.
 Hydrogen and oxygen isotope analyses have been made of hydrous minerals in gabbros and basaltic xenoliths from the Eocene Kap Edvard Holm intrusive complex of East Greenland. The analyzed samples are of three types: (1) primary igneous hornblendes and phlogopites that crystallized from partial melts of hydrothermally altered basaltic xenoliths, (2) primary igneous hornblendes that formed during late–magmatic recrystallization of layered gabbroic cumulates, and (3) secondary actinolite, epidote and chlorite that formed during subsolidus alteration of both xenoliths and gabbros. Secondary actinolite has a δ18O value of −5.8‰ and a δD value of −158‰. These low values reflect subsolidus alteration by low–δ18O, low–δD hydrothermal fluids of meteoric origin. The δD value is lower than the −146 to −112‰ values previously reported for amphiboles from other early Tertiary meteoric–hydrothermal systems in East Greenland and Scotland, indicating that the meteoric waters at Kap Edvard Holm were isotopically lighter than typical early Tertiary meteoric waters in the North Atlantic region. This probably reflects local climatic variations caused by formation of a major topographic dome at about the time of plutonism and hydrothermal activity. The calculated isotopic composition of the meteoric water is δD=−110 ± 10‰, δ18O ≈−15‰. Igneous hornblendes and phlogopites from pegmatitic pods in hornfelsed basaltic xenoliths have δ18O values between −6.0 and −3.8‰ and δD values between −155 and −140‰. These are both much lower than typical values of fresh basalts. The oxygen isotope fractionations between pegmatitic hornblendes and surrounding hornfelsic minerals are close to equilibrium fractionations for magmatic temperatures, indicating that the pegmatites crystallized from low–δ18O partial melts of xenoliths that had been hydrothermally altered and depleted in 18O prior to stoping. The pegmatitic minerals may have crystallized with low primary δD values inherited from the altered country rocks, but these values were probably overprinted extensively by subsolidus isotopic exchange with low–δD meteoric–hydrothermal fluids. This exchange was facilitated by rapid self–diffusion of hydrogen through the crystal structures. Primary igneous hornblendes from the plutonic rocks have δ18O values between +2.0 and +3.2‰ and δD values between −166 and −146‰. The 18O fractionations between hornblendes and coexisting augites are close to equilibrium fractionations for magmatic temperatures, indicating that the hornblendes crystallized directly from the magma and subsequently underwent little or no oxygen exchange. The hornblendes may have crystallized with low primary δD values, due to contamination of the magma with altered xenolithic material, but the final δD values were probably controlled largely by subsolidus isotopic exchange. This inference is based partly on the observation that coexisting plagioclase has been extensively depleted in 18O via a mineral–fluid exchange reaction that is much slower than the hydrogen exchange reaction in hornblende. It is concluded that all hydrous minerals in the study area, whether igneous or secondary, have δD values that reflect extensive subsolidus isotopic equilibration with meteoric–hydrothermal fluids. Received: 22 March 1994 / Accepted: 26 January 1995  相似文献   

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