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1.
G.B. Piccardo  L. Guarnieri 《Lithos》2011,124(3-4):200-214
Hundred-meter wide cumulate bodies and decimetric dykelets of gabbro-norites are widespread within the distal ophiolitic peridotites from the Jurassic Ligure-Piemontese oceanic basin, now emplaced in the Alpine–Apennine orogenic system. These peridotites derived from the sub-continental mantle of the pre-Triassic Europe–Adria lithosphere and underwent profound modifications of their structural and compositional characteristics via melt–rock interaction during diffuse percolation by porous flow of upwelling asthenospheric melts. Gabbro-norite cumulates show the peculiar association of high forsteritic olivine, high-Mg# clinopyroxenes and orthopyroxenes and high anorthitic plagioclase with respect to mineral compositions in common ophiolitic and oceanic MORB gabbros. Abundance and early crystallization of magnesian orthopyroxene suggests that parental magmas of the gabbro-noritic cumulates were relatively silica-rich basaltic liquids. Clinopyroxenes and plagioclase have anomalously low Sr and LREE, resulting in highly fractionated C1-normalized LREE patterns in clinopyroxenes and negatively fractionated C1-normalized LREE patterns in plagioclases.Modal mineralogy and mineral major and trace element compositions indicate that these gabbro-norites crystallized from MORB-type basaltic liquids that were strongly depleted in Na, Ti, Zr, Sr and other incompatible trace elements relative to any erupted liquids of MORB-type ophiolites and modern oceanic lithosphere. Computed melt compositions in equilibrium with gabbro-norite clinopyroxenes are closely similar to depleted MORB-type single melt increments after 5–7% of fractional melting of a DM asthenospheric mantle source under spinel-facies conditions.Present knowledge on the ophiolitic peridotites of Monte Maggiore indicate that they were formed by interaction of lithospheric mantle protoliths with depleted, MORB-type single melt increments produced by the ascending asthenosphere. Their composition was progressively modified from olivine-saturated to orthopyroxene-saturated by the early reactive melt–peridotite interaction (i.e., pyroxene dissolution and olivine precipitation).Gabbro-norite cumulates marked the change from diffuse porous flow percolation to intrusion and crystallization when cooling by conducive heat loss became dominant on heating by melt percolation. Progressive upwelling and cooling of the host peridotite during rifting caused transition to more brittle conditions and to hydration and serpentinization.The Monte Maggiore peridotite body was then intruded along fractures by variably evolved, Mg–Al- to Fe–Ti-rich gabbroic dykes. Computed melt compositions in equilibrium with clinopyroxenes from less evolved gabbro dykes are closely similar to aggregated MORBs. The event of gabbro intrusion indicates that aggregated MORB-type liquids: i) migrated through and stagnated in the mantle lithosphere and ii) underwent evolution into shallow ephemeral magma chambers to form the parental magmas of the gabbroic dykes and the basaltic lava flows of the Ligurian oceanic crust.  相似文献   

2.
Reequilibration of chromite within Kilauea Iki lava lake,Hawaii   总被引：11，自引：0，他引：11  
Chromite mainly occurs as tiny inclusions within or at the edges of olivine phenocrysts in the 1959 Kilauea Iki lava lake. Liquilus chromite compositions are only preserved in scoria that was rapidly quenched from eruption temperatures. Analyses of drill core taken from the lava lake in 1960, 1961, 1975, 1979, and 1981 show that chromite becomes richer in Fe+2, Fe+3, Ti and poorer in Mg, Al, Cr than the liquidus chromite. The amount of compositional change depends on the time elapsed since eruption, the cooling history of the sample, the extent of differentiation of the interstitial melt, and the position of the chromite inclusion within the olivine phenocryst. Compositional changes of the chromite inclusions are thought to be a result of reequilibration with the residual melt by cationic diffusion (Mg, Al, Cr outwards and Fe+2, Fe+3, Ti inwards) through olivine. The changing chemical potential gradients produced as the residual melt cools, crystallizes and differentiates drives the reequilibration process. Major and minor element zoning profiles in olivine phenocrysts suggest that volume diffusion through olivine may have been the major mechanism of cationic transport through olivine. The dramatic compositional changes observed in chromite over the 22 years between eruption and 1981 has major implications for othe molten bodies.  相似文献   

3.
The exceptional occurrence of fluorine-rich mineral phases in the benmoreitic lava dome of Mt. Calvario (south-western flank of Mt. Etna) has given the opportunity to understand the genetic process allowing their crystallization. Both primary and secondary mineral associations were found, namely: plagioclase, clinopyroxene, olivine, fluorapatite and iron oxides as primary assemblage, whereas fluoro-edenite and fluorophlogopite, ferroan-enstatite, hematite, pseudobrookite and tridymite as secondary mineralization. In addition to some major and trace elements (e.g., Fe, Ti, Na, K, P, Ba, Rb, Sm, Zr), particularly fluorine and chlorine concentrations of the whole rock are significantly higher than other Etnean prehistoric benmoreites, and cannot be accounted for common differentiation processes in the feeding system. The selective enrichment in some elements has been here attributed to volatile flushing occurring in the plumbing system, with fluid/melt ratio of ~0.65:1. The resulting high amount of fluorine, coupled with its high solubility even at low pressure for benmoreitic melts, finally led to nucleation and growth of F-rich mineral phases during syn- and post-eruptive conditions.  相似文献   

4.
The late Pleistocene caldera complex of the Sierra La Primavera, Jalisco, México, contains well-exposed lava flows and domes, ash-flow tuff, air-fall pumice, and caldera-lake sediments. All eruptive units are high-silica rhyolites, but systematic chemical differences correlate with age and eruptive mode. The caldera-producing unit, the 45-km3 Tala Tuff, is zoned from a mildly peralkaline first-erupted portion enriched in Na, Rb, Cs, Cl, F, Zn, Y, Zr, Hf, Ta, Nb, Sb, HREE, Pb, Th, and U to a metaluminous last-erupted part enriched in K, LREE, Sc, and Ti; Al, Ca, Mg, Mn, Fe, and Eu are constant within analytical errors. The earliest post-caldera lava, the south-central dome, is nearly identical to the last-erupted portion of the Tala Tuff, whereas the slightly younger north-central dome is chemically transitional from the south-central dome to later, moremafic, ring domes. This sequence of ash-flow tuff and domes represents the tapping of progressively deeper levels of a zoned magma chamber 95,000 ± 5,000 years ago. Since that time, the lavas that erupted 75,000, 60,000, and 30,000 years ago have become decreasingly peralkaline and progressively enriched only in Si, Rb, Cs, and possibly U. They represent successive eruption of the uppermost magma in the post-95,000-year magma chamber.Eruptive units of La Primavera are either aphyric or contain up to 15% phenocrysts of sodic sanidine quartz >ferrohedenbergite >fayalite>ilmenite±titanomagnetite. Whereas major-element compositions of sanidine, clinopyroxene, and fayalite phenocrysts changed only slightly between eruptive groups, concentrations of many trace elements changed by factors of 5 to 10, resulting in crystal/glass partition coefficients that differ by factors of up to 20 between successively erupted units. The extreme variations in partitioning behavior are attributed to small changes in bulk composition of the melt because major-element compositions of the phenocrysts and temperature, pressure, and oxygen fugacity of the magma all remained essentially constant.Crystal settling and incremental partial melting by themselves appear incapable of producing either the chemical gradients within the Tala Tuff magma chamber or the trends with time in the post-caldera lavas. Transport of trace metals as volatile complexes within the thermal and gravitational gradient in volatilerich but water-undersaturated magma is considered the dominant process responsible for compositional zonation in the Tala Tuff. The evolution of the post-caldera lavas with time is thought to involve the diffusive emigration of trace elements from a relatively dry magma as a decreasing proportion of network modifiers and/or a decreasing concentration of complexing ligands progressively reduced trace-metal-site availability in the silicate melt.  相似文献   

5.
Mount Erebus is an active volcano in Antarctica located on Ross Island. A convecting lava lake occupies the summit crater of Mt. Erebus. Since December 1980 the seismic activity of Mt. Erebus has been continuously monitored using a radio-telemetered network of six seismic stations. The seismic activity observed by the Ross Island network during the 1982–1983 field season shows that: (1)Strombolian eruptions occur frequently at the Erebus summit lava lake at rates of 2–5 per day; (2)centrally located earthquakes map out a nearly vertical, narrow conduit system beneath the lava lake; (3)there are other source regions of seismicity on Ross Island, well removed from Mt. Erebus proper. An intense earthquake swarm recorded in October 1982 near Abbott Peak, 10 km northwest of the summit of Mt. Erebus, and volcanic tremor accompanying the swarm, may have been associated with new dike emplacement at depth.  相似文献   

6.
Lead isotope variability in olivine-hosted melt inclusions from Iceland   总被引：2，自引：0，他引：2  
The lead isotope and trace element compositions of a suite of olivine-hosted melt inclusions in primitive lava flows from the Reykjanes Peninsula in Iceland show extreme variability. Much of this variability is present in the composition of inclusions from one hand specimen of Háleyjabunga, a depleted picrite lava shield that erupted 13 ka. 208Pb/206Pb compositions in this sample span 50-90% of the total range found in Atlantic MORB, indicating that high-amplitude compositional heterogeneity is present in the mantle source of melts that aggregated to form a single eruption. The trace element and isotopic trends in the melt inclusions are coincident with those in whole rock samples from young lava flows of the Reykjanes Peninsula, and extend the total range of variation towards more depleted compositions. The incompatible trace element and lead isotope compositions of the inclusions are strongly coupled and lie close to binary mixing trends between the extreme melt inclusion compositions. These relationships indicate that the trace element variation in the melt inclusions reflects heterogeneity in the composition of the mantle source entering the melting region under the Reykjanes Peninsula. Large positive Sr concentration anomalies are present in three of the inclusions, but do not correlate with indicators of mantle melting or source variations and are likely to arise by reaction with plagioclase during crustal storage. Fractional melting of heterogeneous mantle is predicted to generate melts with a wide range of compositions, filling a large volume in trace element-isotope space. However, the compositional variations observed in the melt inclusions lie close to binary mixing curves. These observations may be accounted for by a two-stage model of melt mixing. The first stage occurs in porous channels that transport melt in the mantle and takes place before inclusion entrapment. This mixing stage generates a bimodal distribution of melt compositions that is supplied from the channels to sub-Moho and lower crustal magma lenses. The second stage of mixing occurs in these chambers, producing the binary mixing trends recorded in the inclusion compositions. The distribution of isotopic compositions observed in the melt inclusions and whole rock samples from the Reykjanes Peninsula is therefore controlled by melt mixing. These results have important implications for the interpretation of basalt composition in terms of distinct compositional entities within the upwelling solid mantle under mid-ocean ridges and ocean islands.  相似文献   

7.
Rock textures commonly preserve a record of the near-surface crystallization history of volcanic rocks. Under conditions of simple cooling without convection or mixing, textures will reflect sample cooling rate, the temperature at which crystallization was initiated, and the distribution of mineral phase precipitation across the crystallization interval. Compilation of plagioclase size and number density data on natural (dike, sill and lava lake) and experimental samples suggests that (1) growth and nucleation rates of plagioclase in natural basaltic samples are a predictable function of cooling rate, and (2) the observed crystallization rate dependence on cooling rate is similar to that observed in experiments initiated at subliquidus temperatures. Comparison of natural and experimental samples thus suggests that most basalts crystallize under conditions of heterogeneous nucleation, with the number density of preexisting nucleii partially controlling textural responses to cooling rate changes. Time scales of crystallization and cooling in magmatic systems are intimately linked through a balance between heat removal from the system and heat evolved through crystallization. Evaluation of textural data in the context of recent numerical models of crystallization in simple (one- and two-component systems) provides new insight into regularities in the crystallization behavior of basaltic magmas. For example, the rate of change in crystal size (and number density, as dictated by mass balance) has been used as a measure of the relative importance of time scales of crystallization and cooling in numerical models of crystallizing systems. In natural samples, plagioclase size scales with the length scale of cooling such that a logarithmic plot of grain size as a function of normalized distance across the dike has a slope that appears approximately independent of dike width (solidification time). Comparison with available textural data for other phenocryst phases suggests that the same may be true for pyroxene and magnetite crystallization, with each phase having a characteristic slope probably controlled by the thermodynamic properties of the crystallizing phase. Measured crystal size distributions are unimodal and show maximum frequencies in the smaller size classes; distributions broaden and the grain size at peak frequency increases with increasing crystallization times (decreasing cooling rates). In contrast, partially crystallized Makaopuhi lava lake samples have crystal size distributions that decrease exponentially with increasing crystal size. Measured size distributions in dikes can be explained by late stage modification of Makaopuhi-type distributions through loss of small crystals, possibly the consequence of growth without nucleation. Finally, this compilation of the textural response of basaltic magmas to changes in cooling rate suggests that empirical calibrations of crystallization rate dependence on cooling rate from natural samples provide a reasonable model for plagioclase crystallization in near-surface basaltic systems. Predicted growth rates will be slow and relatively constant (10-10–10-11 cm/s) for crystallization times expected in most shallow volcanic systems (<1000 years).  相似文献   

8.
西藏白朗地区蛇绿岩火山岩中单斜辉石的化学特征   总被引：2，自引：0，他引：2       下载免费PDF全文
近年来,应用岩石的地球化学和矿物学特征区分不同构造位置的现代火山岩,已被人们所注意。同时,根据这种观测资料所确定的一般特征,亦已广泛地应用于古火山岩,并获得了一些古地质环境的概念。  相似文献   

9.
The least-altered, Permian mafic volcanic rocks from the Pang Mayao area, Phrao District, Chiang Mai Province, part of Chiang Rai–Chiang Mai volcanic belt, have been analyzed and are found to be mid-ocean ridge and ocean–island basalts. The mid-ocean ridge basalts occur as lava flows or dike rocks. They are equigranular, fine- to medium-grained and consist largely of plagioclase, clinopyroxene and olivine. These basalt samples are tholeiitic, and have compositions very similar to T-MORB from the region where the Du Toit Fracture Zone intersects the Southwest Indian Ridge. The ocean–island basalt occurs as pillow breccia, and lava flows or dike rocks. They are slightly to moderately porphyritic, with phenocrysts/microphenocrysts of clinopyroxene, olivine, plagioclase and/or Fe–Ti oxide. The groundmass is very fine-grained, and made up largely of felty plagioclase laths with subordinate clinopyroxene. These basalt samples are alkalic, and chemically analogous to those from Haleakala Volcano, Maui, Hawaiian Chain. These mafic volcanic rocks may have been formed in a major ocean basin rather than in a mature back-arc basin.  相似文献   

10.
We present field relationships, petrography, and mineral major and trace element data for the Neoproterozoic Dariv Igneous Complex of the Altaids of Western Mongolia. This unique complex of high-K plutonic rocks is composed of well-exposed, km-scale igneous intrusions of wehrlites, phlogopite wehrlites, apatite-bearing phlogopite clinopyroxenites, monzogabbros, monzodiorites, and clinopyroxene-bearing monzonites, all of which are intruded by late stage lamprophyric and aplitic dikes. The biotite-dominated igneous complex intrudes depleted harzburgitic serpentinite. The observed lithological variability and petrographic observations suggest that the plutonic rocks can be ascribed to a fractionation sequence defined by olivine + clinopyroxene ± Fe–Ti oxides → phlogopite + apatite → K-feldspar + plagioclase → amphibole + quartz. Notably, phlogopite is the dominant hydrous mafic mineral. Petrogenesis of the observed lithologies through a common fractionation sequence is supported by a gradual decrease in the Mg# [molar Mg/(Fetotal + Mg) × 100] of mafic minerals. Crystallization conditions are derived from experimental phase petrology and mineral chemistry. The most primitive ultramafic cumulates crystallized at ≤0.5 GPa and 1,210–1,100 °C and oxygen fugacity (fO2) of +2–3 ?FMQ (log units above the fayalite–quartz–magnetite buffer). Trace element modeling using clinopyroxene and apatite rare earth element compositions indicates that the dominant mechanism of differentiation was fractional crystallization. The trace element composition of a parental melt was calculated from primitive clinopyroxene compositions and compares favorably with the compositions of syn-magmatic lamprophyres that crosscut the fractionation sequence. The parental melt composition is highly enriched in Th, U, large ion lithophile elements, and light rare earth elements and has a pronounced negative Nb–Ta depletion, suggestive of an alkaline primitive melt originating from a subduction-imprinted mantle. Comparison with a global compilation of primitive arc melts demonstrates that Dariv primitive melts are similar in composition to high-K primitive melts found in some continental arcs. Thus, the high-K fractionation sequence exposed in the Dariv Igneous Complex may be a previously unrecognized important fractionation sequence resulting in alkali-rich upper crustal granitoids in continental arc settings.  相似文献   

11.
This study documents the petrography and whole-rock major and trace element geochemistry of 38 samples mainly from a drill core through the entire Fedorivka layered intrusion (Korosten Pluton), as well as mineral compositions (microprobe analyses and separated mineral fraction analyses of plagioclase, ilmenite, magnetite and apatite) of 10 samples. The Fedorivka layered intrusion can be divided into 4 lithostratigraphic units: a Lower Zone (LZ, 72 m thick), a Main Zone (MZ, 160 m thick), and an Upper Border Zone, itself subdivided into 2 sub-zones (UBZ2, 40 m thick; UBZ1, 50 m thick). Igneous lamination defines the cumulate texture, but primary cumulus minerals have been affected by trapped liquid crystallization and subsolidus recrystallization. The dominant cumulus assemblage in MZ and UBZ2 is andesine (An39–42), iron-rich olivine (Fo32–42), augite (En29–35Fs24–29Wo42–44), ilmenite (Hem1–6), Ti-magnetite (Usp52–78), and apatite. The data reveal a continuous evolution from the floor of the intrusion (LZ) to the top of MZ, due to fractional crystallization, and an inverse evolution in UBZ, resulting from crystallization downwards from the roof. The whole-rock Fe/Mg ratio and incompatible element contents (e.g. Rb, Nb, Zr, REE) increase in the fractionating magma, whereas compatible elements (e.g. V, Cr) steadily decrease. The intercumulus melt remained trapped in the UBZ cumulates due to rapid cooling and lack of compaction, and cumulus mineral compositions re-equilibrated (e.g. olivine, Fe–Ti oxides). In LZ, the intercumulus melt was able to partially or totally escape. The major element composition of the MZ cumulates can be approximated by a mixing (linear) relationship between a plagioclase pole and a mafic pole, the latter being made up of all mafic minerals in (nearly) constant relative proportions. By analogy with the ferrobasaltic/jotunitic liquid line of descent, defined in Rogaland, S. Norway, and its conjugated cumulates occurring in the Transition Zone of the Bjerkreim-Sokndal intrusion (Rogaland, a monzonitic (57% SiO2) melt is inferred to be in equilibrium with the MZ cumulates. The conjugated cumulate composition falls (within error) on the locus of cotectic compositions fixed by the 2-pole linear relationship. Ulvöspinel is the only Ti phase in some magnetites that have been protected from oxidation. QUIlF equilibria in these samples show that magnetite and olivine in MZ have retained their liquidus compositions during subsolidus cooling. This permits calculation of liquidus fO2 conditions, which vary during fractionation from ΔFMQ = 0.7 to − 1.4 log units. Low fO2 values are also evidenced by the late appearance of cumulus magnetite (Fo42) and the high V3+-content of the melt, reflected in the high V-content of the first liquidus magnetite (up to 1.85% V).  相似文献   

12.
The partition of Si, Al, Ti, Fe3+, Mg, Fe2+, Mn, Ca and Na between coexisting Ca-rich and Ca-poor pyroxenes from a wide variety of igneous and metamorphic rocks have been investigated systematically. Many of the distributions, and especially those for the partition of Ti, Mg, Fe2+, Mn and Na, indicate characteristic trends for pyroxenes from the various petrologic groups identified. The partition of Mg, Fe2+ and Mn correlate with inferred cooling rates, the partition co-efficients of pyroxenes from extruded and other quickly cooled rocks most nearly approaching unity. In contrast, the partition of Si and Ti and the absolute amounts of Al may be related to the physicochemical conditions prevailing during original crystallisation; Ti being particularly relatively enriched in Ca-rich pyroxenes of ultramafic associations. The trends of the compositions of the Ca-rich pyroxenes plotted in the pyroxene quadrilateral also correlate with cooling rates and comparison with the limited data available on the phase relations of coexisting pyroxenes suggests that sub-solidus chemical readjustments have occurred in both phases.  相似文献   

13.
The compositional variation of clinopyroxene and the partitioning of major elements between clinopyroxene and melt are estimated as a function of the cooling rate. Clinopyroxenes were crystallized under variable cooling regimes (15, 9.4, 3, 2.1, and 0.5 °C/min from 1250 down to 1000 °C) and at isothermal conditions of 1000 °C from a basaltic composition at a pressure of 500 MPa under anhydrous and hydrous (H2O = 1.3 wt.%) conditions. The clinopyroxene chemistry shows that, as the cooling rate increases, crystals are progressively depleted in Ca, Mg, Fe2+ and Si and enriched in Na, Fe3+, Al (mainly AlIV), and Ti. Di and Hd versus CaTs and CaFeTs form a continuous binary solid solution characterized by higher amounts of tschermakitic components with increasing cooling rate. Two parameters (DH = Di + Hd and TE = CaTs + CaFeTs + En) are calculated to describe the effect of cooling rate on the clinopyroxene composition. The variation of DH/TE with increasing cooling rate evidences the kinetic process induced by rapid cooling in basic rocks under hydrous and anhydrous conditions.Dynamic crystallization conditions affect the partitioning of major elements between clinopyroxene and melt; with increasing cooling rate, the value of crystal–melt partition coefficient departs from that obtained at the isothermal condition. However, in spite of these variations, the values of cpx–meltKdFe–Mg remain almost constant. Therefore, the Fe2–Mg exchange between clinopyroxene and melt is not suitable to prove the (dis)equilibrium conditions in basaltic cooling magmas, giving rise to possible mismatches in the application of thermobarometers. The results of our study are consistent with that observed at the margin of dikes or in the exterior portions of lavas, where the cooling rate is maximized and disequilibrium compositions of clinopyroxene have been found.  相似文献   

14.
The Laki eruption involved 10 fissure-opening episodes thatproduced 15·1 km3 of homogeneous quartz-tholeiite magma.This study focuses on the texture and chemistry of samples fromthe first five episodes, the most productive period of the eruption.The samples comprise pumiceous tephra clasts from early falloutdeposits and lava surface samples from fire-fountaining andcone-building activity. The fluid lava core was periodicallyexposed at the surface upon lobe breakout, and its characteristicsare preserved in glassy selvages from the lava surface. In allsamples, plagioclase is the dominant mineral phase, followedby clinopyroxene and then olivine. Samples contain <7 vol.% of euhedral phenocrysts (>100 µm) with primitivecores [An* = 100 x Ca/(Ca + Na) >70; Fo > 75; En* = 100x Mg/(Mg + Fe) >78] and more evolved rims, and >10 vol.% of skeletal, densely distributed groundmass crystals (<100µm), which are similar in composition to phenocryst rims(tephra: An*58–67, Fo72–78, En*72–81; lava:An*49–70, Fo63–78, En57–78). Tephra and lavahave distinct vesicularity (tephra: >40 vol. %; lava: <40vol. %), groundmass crystal content (tephra: <10 vol. %;lava: 20–30 vol. %), and matrix glass composition (tephra:5·4–5·6 wt % MgO; lava: 4·3–5·0wt % MgO). Whole-rock and matrix glass compositions define atrend consistent with liquid evolution during in situ crystallizationof groundmass phases. Plagioclase–glass and olivine–glassthermometers place the formation of phenocryst cores at 10 kmdepth in a melt with 1 wt % H2O, at near-liquidus temperatures(1150°C). Phenocryst rims and groundmass crystals formedclose to the surface, at 10–40°C melt undercoolingand in an 10–20°C cooler drier magma (0–0·1wt % H2O), causing an 10 mol % drop in An content in plagioclase.The shape, internal zoning and number density of groundmasscrystals indicate that they formed under supersaturated conditions.Based on this information, we propose that degassing duringascent had a major role in rapidly undercooling the melt, promptingintensive shallow groundmass crystallization that affected themagma and lava rheology. Petrological and textural differencesbetween tephra and lava reflect variations in the rates of magmaascent and the timing of surface quenching during each eruptiveepisode. That in turn affected the time available for crystallizationand subsequent re-equilibration of the melt to surface (degassed)conditions. During the explosive phases, the rates of magmaascent were high enough to inhibit crystallization, yieldingcrystal-poor tephra. In contrast, pervasive groundmass crystallizationoccurred in the lava, increasing its yield strength and causinga thick rubbly layer to form during flow emplacement. Lava selvagescollected across the flow-field have strikingly homogeneousglass compositions, demonstrating the high thermal efficiencyof fluid lava transport. Cooling is estimated as 0·3°C/km,showing that rubbly surfaced flows can be as thermally efficientas tube-fed phoehoe lavas. KEY WORDS: lava; crystallization; basalt; cooling rate; pressure; geobarometry; P–T conditions; plagioclase; degassing; Laki, Iceland  相似文献   

15.
Materials balance calculations are presented to document the progressive bulk chemical changes in metagreywacke and metapelite with separation of increments of granite of minimum melt composition. During partial melting, enrichment of Fe relative to Mg in granite and strong absorption of water leave residual rocks with increasing proportions of such Mg-rich phases as cordierite and progressively dehydrated. Extraction of most granitic compositions from metapelites results in increasing the Al value of residua, while extraction of an alkali granite melt from metagreywacke is necessary to change the Al values in their residua (from peraluminous to sub- or metaluminous). Under essentially constant temperature conditions, complex isograds may develop locally reflecting the bulk chemical changes produced by melt removal. Natural amphibolite/granulite facies rocks from three locations in Canada are compared with the calulated trends.  相似文献   

16.
 The use of ocean floor basalt chemistry as a tool to investigate mantle composition and processes requires that we work with basalts that have been modified little since leaving the mantle. One source of such basalts is melt inclusions trapped in primitive crystals. However, obtaining information from these melt inclusions is complicated by the fact that melt inclusions in natural basalts are essentially always altered by post-entrapment crystallization. This requires that we develop techniques for reconstructing the original trapped liquid compositions. We conducted a series of experiments to reverse the effects of post-entrapment crystallization by re-heating the host crystals to their crystallization temperature. For these experiments we used plagioclase crystals separated from a single Gorda Ridge lava. The crystallization temperature for these crystals was determined by a set of incremental re-heating experiments to be ∼1240–1260° C. The inclusions are primitive, high Ca-Al basaltic melts, saturated with plagioclase, olivine and Al-rich chromite at low pressure. The inclusion analyses can be linked to the host lava composition by low pressure fractionation. The major element composition of the re-homogenized melt inclusions within each crystal is relatively constant. However, the incompatible element analyses have extremely wide ranges. The range of La/Sm and Ti/Zr from inclusions analyzed from a single sample from the Gorda Ridge exceeds the range reported for lavas sampled from the entire ridge. The pyroxene compositions predicted to be in equilibrium with the melt inclusion trace element signature cover much of the range represented by pyroxenes from abyssal peridotites. The volumetric proportions of the magmas entering the base of the crust can be evaluated using frequency distribution of melt inclusion compositions. This distribution suggests that the array of magmas was skewed towards the more depleted compositions, with little evidence for an enriched component in this system. This pattern is more consistent with a dynamic flow model of the mantle or of a passive flow model where the melts produced in the peripheral areas of the melting regime were not focused to the ridge. Received: 5 January 1995 / Accepted: 13 June 1995  相似文献   

17.
Magma mixing can occur in a fluid manner to produce banded pumice or in a brittle manner to form enclaves. We propose that the critical control on mixing style is a competition between developing networks of crystals in the intruding magma that impart a strength to the magma and melting and disrupting those networks in the host. X-ray computed tomography analysis demonstrates that banded pumice from the 1915 Mt. Lassen eruption lacks crystal networks. In contrast, rhyodacite hosts with mafic enclaves from Chaos Crags contain well-developed networks of large crystals. We present a one-dimensional conductive cooling model that predicts mixing style, either ductile or brittle, as a function of magma compositions, temperatures, and the size of the intruding dike. Our model relies on three assumptions: (1) Mixing is initiated by the injection of a hot dike into a cooler magma body with a yield strength; (2) when magma crystallinity exceeds a critical value, 13 vol% plagioclase, the magma develops a yield strength; and (3) when total crystallinity exceeds 40 vol%, the magma has a penetrative crystal network and is effectively solid. Importantly, because the two magmas are of different compositions, their crystallinities and viscosities do not have the same variations with temperature. As the intruding magma cools, it crystallizes from the outside in, while simultaneously, host magma temperature near the intruder rises. Mixing of the two magmas begins when the host magma is heated sufficiently to (1) disrupt the crystal network and (2) initiate convection. If the shear stress exerted by the convecting host magma on the dike is greater than the yield strength of the dike margin (and dike crystallinity does not exceed 40 %), then fluid mixing occurs, otherwise enclaves form by brittle deformation of the dike. Application of the model to magma compositions representative of Lassen and Chaos Crags shows that emplacement of dikes <1 m thick should produce enclaves, whereas thicker dikes should generate fluid mixing and form banded pumice within days to weeks of emplacement. Similar relationships apply to other modeled magmatic systems, including Pinatubo, Unzen, and Ksudach/Shtuybel’ volcanoes. For all studied systems, the absolute size of the intruding dike, not just its proportion relative to the host, influences mixing style.  相似文献   

18.
The town of Zafferana Etnea, located on the southeastern slope of Mt. Etna volcano (Italy), has been repeatedly threatened by lava flows in recent centuries. The last serious threat occurred during the 1991–1993 eruption, when the lava front came to a halt only 1.7 km from the centre of town. Morphostructural data derived from light detection and ranging (LiDAR) surveys carried out on Etna in 2005 have enabled us to evaluate the risk of lava invasion in a section (16 km2) of the Zafferana Etnea territory. Qualitative and quantitative results are obtained combining the information derived from LiDAR analysis with geological, morphological and structural data using geographic information systems technology (GIS). The study quantifies in unprecedented detail the areal extent and volume of forested and urban areas and its degree of exposure to different levels of hazard from future lava invasion. Nearly 52% of the urban texture fall into areas of moderate to high risk from lava invasion. Future land use planning should take these findings into account and promote new development preferentially in areas of lower risk.  相似文献   

19.
We simulated the process of magma–carbonate interaction beneath Mt. Vesuvius in short duration piston-cylinder experiments under controlled magmatic conditions (from 0 to 300 s at 0.5 GPa and 1,200 °C), using a Vesuvius shoshonite composition and upper crustal limestone and dolostone as starting materials. Backscattered electron images and chemical analysis (major and trace elements and Sr isotopes) of sequential experimental products allow us to identify the textural and chemical evolution of carbonated products during the assimilation process. We demonstrate that melt–carbonate interaction can be extremely fast (minutes), and results in dynamic contamination of the host melt with respect to Ca, Mg and 87Sr/86Sr, coupled with intense CO2 vesiculation at the melt–carbonate interface. Binary mixing between carbonate and uncontaminated melt cannot explain the geochemical variations of the experimental charges in full and convection and diffusion likely also operated in the charges. Physical mixing and mingling driven by exsolving volatiles seems to be a key process to promote melt homogenisation. Our results reinforce hypotheses that magma–carbonate interaction is a relevant and ongoing process at Mt. Vesuvius and one that may operate not only on a geological, but on a human timescale.  相似文献   

20.
The quasiequilibrium directed crystallization technique was used for experimental simulation of zoning characteristic of Cu-rich pyrrhotite-chalcopyrite and pyrrhotite-cubanite-mooihoekite-haycockite ores at the Oktyabr??sky deposit. Directed crystallization of samples I (Fe 32.55, Cu 10.70, Ni 5.40, S. 51.00, Pt = Pd = Rh = Ir= Au = Ag = 0.05 at %) and II (Fe 33.74, Cu 15.94, Ni 1.48, S. 48.75, Pt = Pd = 0.05 at %) was performed. These samples approximate average composition of the ore. Monosulfide (mms) and intermediate (iss) solid solutions progressively crystallized from the melt. The curves of ore element distribution in samples have been drawn. The partition coefficients (k) of ore elements between solid solutions and sulfide melt have been determined depending on melt composition. The paths of melt, mss, and iss compositions are supplemented by tie lines connecting compositions of equilibrium liquid and solid phases. The phase composition of samples after cooling was studied using an optical microscope, XRD, and microprobe. The zoning of sample I is described by the following sequence of phases: monoclinic pyrrhotite ?? hexagonal pyrrhotite + tetragonal chalcopyrite ?? tetragonal and cubic chalcopyrite + pentlandite + bornite. Crystallized sample II consists of four zones: (1) hexagonal pyrrhotite and isocubanite; (2) hexagonal pyrrhotite, cubanite, and pentlandite; (3) low-S pc-phase close to haycockite and pentlandite; and (4) mooihoekite, pentlandite, and bornite mixtures. This sequence corresponds to the secondary zoning, which reflects both the primary fractionation of components and the solid-phase reactions during cooling of the crystallized sample. The Rh, Ru, and Ir partition coefficients between mss and melt have been measured, and speciation of PGM in samples has been identified. The results obtained are compared with typical natural Cu-rich sulfide ore of the Oktyabr??sky deposit.  相似文献   

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