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1.
The investigation of rocks, minerals, and melt inclusions showed that porphyritic alkaline picrites and meimechites crystallized from different parental magmas. At a similar ultrabasic composition, the alkaline picrite melts were enriched in K2O relative to Na2O, and contained up to 0.12–0.13 wt % F and less Cr, Ni, and H2O (only 0.01–0.16 wt % H2O, versus 0.6–1.6 wt % in the meimechite melts) compared with the meimechite magmas. The crystallization of alkaline picrite melts occurred under stable conditions at relatively low temperatures without abrupt changes: olivine and clinopyroxene crystallized at 1340–1285 and 1230–1200°C, respectively, as compared with 1600–1450 and 1230–1200°C in the meimechites. The alkaline picrite melts evolved toward melanephelinite, nephelinite, tephrite, and trachydolerite; whereas the meimechite magmas gave rise to subalkaline picritic rocks. The partitioning of vanadium between olivine and melt suggests that the meimechite magma crystallized under more oxidizing conditions compared with the alkaline picrite melts: the KDV values for the meimechite melts (0.011–0.016) were three times lower than those for the alkaline picrite melts (0.045–0.052). The parental magmas of the alkaline picrites and meimechites were enriched in trace elements relative to mantle levels by factors of tens to hundreds. The alkaline picrite magma showed lower LILE and LREE contents compared with the meimechite magma. The magmas had also different indicator ratios of incompatible elements, including those immobile in aqueous fluids. It was concluded that the meimechite and alkaline picrite melts were derived from different mantle sources. The former were generated at lower degrees of melting of an undepleted mantle source, and the meimechite melts were produced by high-degree melting of a probably lherzolite-harzburgite source.  相似文献   

2.
The evolution of a carbonated nephelinitic magma can be followed by the study of a statistically significant number of melt inclusions, entrapped in co-precipitated perovskite, nepheline and magnetite in a clinopyroxene- and nepheline-rich rock (afrikandite) from Kerimasi volcano (Tanzania). Temperatures are estimated to be 1,100°C for the early stage of the melt evolution of the magma, which formed the rock. During evolution, the magma became enriched in CaO, depleted in SiO2 and Al2O3, resulting in immiscibility at ~1,050°C and crustal pressures (0.5–1 GPa) with the formation of three fluid-saturated melts: an alkali- and MgO-bearing, CaO- and FeO-rich silicate melt; an alkali- and F-bearing, CaO- and P2O5-rich carbonate melt; and a Cu–Fe sulfide melt. The sulfide and the carbonate melt could be physically separated from their silicate parent and form a Cu–Fe–S ore and a carbonatite rock. The separated carbonate melt could initially crystallize calciocarbonatite and ultimately become alkali rich in composition and similar to natrocarbonatite, demonstrating an evolution from nephelinite to natrocarbonatite through Ca-rich carbonatite magma. The distribution of major elements between perovskite-hosted coexisting immiscible silicate and carbonate melts shows strong partitioning of Ca, P and F relative to FeT, Si, Al, Mn, Ti and Mg in the carbonate melt, suggesting that immiscibility occurred at crustal pressures and plays a significant role in explaining the dominance of calciocarbonatites (sövites) relative to dolomitic or sideritic carbonatites. Our data suggest that Cu–Fe–S compositions are characteristic of immiscible sulfide melts originating from the parental silicate melts of alkaline silicate–carbonatite complexes.  相似文献   

3.
This paper reviews the results of investigations of melt inclusions in minerals of carbonatites and spatially associated silicate rocks genetically related to various deep-seated undersaturated silicate magmas of alkaline ultrabasic, alkaline basic, lamproitic, and kimberlitic compositions. The analysis of this direct genetic information showed that all the deep magmas are inherently enriched in volatile components, the most abundant among which are carbon dioxide, alkalis, halides, sulfur, and phosphorus. The volatiles probably initially served as agents of mantle metasomatism and promoted melting in deep magma sources. The derived magmas became enriched in carbon dioxide, alkalis, and other volatile components owing to the crystallization and fractionation of early high-magnesium minerals and gradually acquired the characteristics of carbonated silicate liquids. When critical compositional parameters were reached, the accumulated volatiles catalyzed immiscibility, the magmas became heterogeneous, and two-phase carbonate-silicate liquid immiscibility occurred at temperatures of ≥1280–1250°C. The immiscibility was accompanied by the partitioning of elements: the major portion of fluid components partitioned together with Ca into the carbonate-salt fraction (parental carbonatite melt), and the silicate melt was correspondingly depleted in these components and became more silicic. After spatial separation, the silicate and carbonate-silicate melts evolved independently during slow cooling. Differentiation and fractionation were characteristic of silicate melts. The carbonatite melts became again heterogeneous within the temperature range from 1200 to 800–600°C and separated into immiscible carbonate-salt fractions of various compositions: alkali-sulfate, alkali-phosphate, alkali-fluoride, alkali-chloride, and Fe-Mg-Ca carbonate. In large scale systems, polyphase silicate-carbonate-salt liquid immiscibility is usually manifested during the slow cooling and prolonged evolution of deeply derived melts in the Earth’s crust. It may lead to the formation of various types of intrusive carbonatites: widespread calcite-dolomite and rare alkali-sulfate, alkali-phosphate, and alkali-halide rocks. The initial alkaline carbonatite melts can retain their compositions enriched in P, S, Cl, and F only at rapid eruption followed by instantaneous quenching.  相似文献   

4.
We present a comprehensive mineral chemical dataset (～400 analyses) on subalkaline meimechitic (Mg-number?=?74–80) and ferropicritic (Mg-number?=?67–69) dike samples from the Antarctic extension of the Karoo large igneous province (LIP) in Vestfjella, western Dronning Maud Land. Some of the meimechites, previously considered to be cumulates from ferropicritic magmas, are characterized by forsteritic olivine (with core composition up to Fo92) that is in, or close to Fe-Mg equilibrium with the host rock. The olivines are subhedral to euhedral, contain Ti-rich (volcanic) spinel inclusions, have a high CaO content (≥0.19 wt. %), and are thus unlikely to represent xenocrysts from mantle peridotite. Igneous amphibole is found in olivine-hosted, crystallized melt inclusions, indicating that the parental magmas had a H2O content of 1–2 wt. %. The olivine data suggests generation of extremely MgO-rich (up to 25 wt. %) melts during the Karoo magmatism. Based on our petrogenetic modeling, such melts are likely to have originated from the partial melting of garnet peridotite at high pressures (5–6 GPa) and mantle potential temperatures (>1,600°C) that are compatible with the involvement of a mantle plume in the generation of the Karoo LIP. A geochemical comparison of the Vestfjella meimechites with meimechites from the Siberian Traps LIP and the assumed komatiitic parental melts of the Horingbai picrites (Paraná-Etendeka LIP) reveals key similarities, suggesting that all these suites were generated from broadly similar sources and/or by similar melting processes in anomalously hot subcontinental mantle.  相似文献   

5.
Gabbro inclusions from Tindfjallajökull are divided into two types: I. Panidiomorphic gabbros of non-cumulative origin composed of plagioclase + olivine ± clinopyroxene and interstitil vesicular glass. They have formed in equilibrium with the host magma and may either represent a marginal facies or a highly solidified magma body. In the latter case the host magma or part of it could be mobilized interstitial liquid. II. Allotriomorphic-hypidiomorphic tholeiitic olivine gabbro and diorite xenoliths with scarce Ti-pargasite which have undergone less than 10% partial melting in the host magma forming melts of alkali basaltic or Hekla andesite-like compositions dependent on the original mineral assemblage. Such liquids, enriched in K2O and possibly other incompatible elements, may contaminate basaltic magmas rising slowly through a gabbroic lower crust. Large scale production of andesites by partial melting of such rocks is not possible but would need more hydrous or differentiated source rocks.  相似文献   

6.
Melt inclusions in olivine Fo83–72 from tephras of 1867, 1971 and 1992 eruptions of Cerro Negro volcano represent a series of basaltic to andesitic melts of narrow range of MgO (5.6–8 wt %) formed by ~46 wt % fractional crystallization of olivine (~6 wt %), plagioclase (~27 wt %), pyroxene (~13 wt %) and magnetite (<1 wt %) from primitive basaltic melt (average SiO2 = 49 wt %, MgO = 7.6 wt %, H2O = 6 wt %) as it ascended to the surface from the depth of about 14 km. The crystallization occurred at increasing liquidus temperature from 1,050 to 1,090 °C in the pressure range from 400 to 50 MPa and was induced by release of mixed H2O–CO2 fluid from the melt at decreasing pressure. Matrix glass compositions fall at the high-Si end of the melt inclusion trend and represent the final stage of melt crystallization during and after eruption. The bulk compositions of erupted Cerro Negro magmas (tephras and lavas) range from high- to low-MgO (3–10 wt %) basalts, which form a compositional array crossing the trend of melt inclusions so that virtually no rock from Cerro Negro has composition akin to true melt represented by the inclusions. The variations of the bulk magma (rocks) and melt (melt inclusions) compositions can be generated in a dyke connecting a deep primitive magma reservoir with the Cerro Negro edifice. While the melt inclusions represent the compositional trend of instantaneous melts along the magma pathway at decreasing pressure and H2O content, occurrence of low-Mg to high-Mg basalts reflects the process of phenocryst re-distribution in progressively evolving melt. The crystallization scenario is anticipated to operate everywhere in dykes feeding basaltic volcanoes and can explain the predominance of plagioclase-rich high-Al basalts in island arc as well as typical compositional variations of magmas during single eruptions.  相似文献   

7.
The Okete Volcanics form small volume monogenetic volcanoes situated around the flanks of larger tholeiitic cones of the Plio-Pleistocene Alexandra Volcanics, in the back-arc tectonic environment of western North Island, New Zealand. The lavas and tuffs of the Okete Volcanics have compositions which include basanites, alkali olivine basalts, olivine tholeiites, and hawaiites. Most rocks have Mg numbers >66, >250 p.p.m. Ni, >500 p.p.m. Cr, and often contain ultramafic xenoliths, which indicate that they are very close to being primary magmas. The Okete Volcanics show geochemical trends, from basanite to hawaiite, of progressive depletion of both compatible and incompatible trace elements, progressive increase in Al2O3, and heavy REE and Y enrichment with crossingover REE patterns in the hawaiites. These geochemical trends can be accounted for by varying degrees of partial melting of a light REE enriched garnet peridotite with subsequent modification of the melts near source or during ascent by fractional crystallization of olivine and minor clinopyroxene. Mass balance calculations cannot quantitatively constrain the degree of partial melting or fractional crystallization, but nevertheless indicate that the Okete alkali olivine basalts, olivine tholeiites, and hawaiites have been derived by successively larger degrees of partial melting relative to basanites, and have also been progressively more modified by fractional crystallization than have the basanites. Sources of the alkalic melts lay at depths corresponding to >20 kb, and most of the ultramafic xenoliths, apart from some which may be cognate cumulates, are unrelated to the magmas that brought them to the surface. Magmas have changed in composition with time from older smaller-volume volcanoes of basanite or alkali olivine basalt compositions, to younger and more voluminous volcanoes which contain hawaiites. The geochemical trends shown by the Okete Volcanics and their spatial association with voluminous tholeiitic volcanism, are features which are different from those observed elsewhere in the Pliocene to Recent basaltic fields of northern North Island, and may be related to their unique tectonic setting, situated in a distinct structural domain.  相似文献   

8.
The Neoproterozoic Korab Kansi mafic-ultramafic intrusion is one of the largest (100 km2) intrusions in the Southern Eastern Desert of Egypt. The intrusion consists of Fe-Ti-bearing dunite layers, amphibole peridotites, pyroxenites, troctolites, olivine gabbros, gabbronorites, pyroxene gabbros and pyroxene-hornblende gabbros, and also hosts significant Fe-Ti deposits, mainly as titanomagnetite-ilmenite. These lithologies show rhythmic layers and intrusive contacts against the surrounding granites and ophiolitic-island arc assemblages. The wide ranges of olivine forsterite contents (Fo67.9-85.7), clinopyroxene Mg# (0.57–0.95), amphibole Mg# (0.47–0.88), and plagioclase compositions (An85.8-40.9) indicate the role of fractional crystallization in the evolution from ultramafic to mafic rock types. Clinopyroxene (Cpx) has high REE contents (2–30 times chondrite) with depleted LREE relative to HREE, like those crystallized from ferropicritic melts generated in an island-arc setting. Melts in equilibrium with Cpx also resemble ferropicrites crystallized from olivine-rich mantle melts. Cpx chemistry and its host rock compositions have affinities to tholeiitic and calc-alkaline magma types. Compositions of mafic-ultramafic rocks are depleted in HFSE (e.g. Nb, Ta, Zr, Th and U) relative to LILE (e.g. Li, Rb, Ba, Pb and Sr) due to the addition of subduction-related hydrous fluids (rich in LILE) to the mantle source, suggesting an island-arc setting. Fine-grained olivine gabbros may represent quenched melts approximating the primary magma compositions because they are typically similar in assemblage and chemistry as well as in whole-rock chemistry to ferropicrites. We suggest that the Korab Kansi intrusion crystallized at temperatures ranging from ~700 to 1100 °C from ferropicritic magma derived from melting of metasomatized mantle at <5 Kbar. These hydrous ferropicritic melts were generated in the deep mantle and evolved by fractional crystallization under high ƒO2 at relatively shallow depth. Fractionation formed calc-alkaline magmas during the maturation of an island arc system, reflecting the role of subduction-related fluids. The interaction of metasomatized lithosphere with upwelling asthenospheric melts produced the Fe and Ti-rich ferropicritic parental melts that are responsible for precipitating large quantities of Fe-Ti oxide layers in the Korab Kansi mafic-ultramafic intrusion. The other factors controlling these economic Fe-Ti deposits beside parental melts are high oxygen fugacity, water content and increasing degrees of mantle partial melting. The generation of Ti-rich melts and formation of Fe-Ti deposits in few layered intrusions in Egypt possibly reflect the Neoproterozoic mantle heterogeneity in the Nubian Shield. We suggest that Cryogenian-Tonian mafic intrusions in SE Egypt can be subdivided into Alaskan-type intrusions that are enriched in PGEs whereas Korab Kansi-type layered intrusions are enriched in Fe-Ti-V deposits.  相似文献   

9.
The Koetong Suite of Silurian, 2-mica granitoids was derived from a metasedimentary source and emplaced into Ordovician sediments and metasediments along the eastern margin of the Western Metamorphic Belt of South-eastern Australia. Whole-rock geochemical considerations preclude derivation of the magmas represented by the granitoids from exposed Ordovician metasediments. The magmas were generated by partial melting of material similar in composition to garnet-cordierite gneisses exposed in the adjacent metamorphic belt. Melting at pressures in excess of 5 Kb and temperatures about 750°C produced peraluminous magmas and, when the degree of partial melting approached 25–30%, these magmas became mobile and moved vertically into the overlying Ordovician sediments. During movement from the source region to the zone of emplacement, separation of the melt and refractory residue components of the magma resulted in a range of compositions so that whole-rock analyses of the granitoids are linearly related on major and trace element variation diagrams. Processes such as crystal fractionation and crystal accumulation may have operated locally. The magmas were largely composed of solid material throughout their emplacement histories and the amount of melt may not have exceeded 30–45% at any stage. Metasedimentary inclusions are a reflection of source heterogeneity.After emplacement of the magmas, in situ crystallization of a relatively anhydrous assemblage of minerals led to water contents in residual, intercrystalline, melts sufficiently high for muscovite to begin crystallization at pressures around 4 Kb. Subsequent saturation of intercrystalline residual melt and loss of the resultant volatile phase caused the development of eutectoid intergrowths involving muscovitebiotite-quartz and alkali feldspar.  相似文献   

10.
Kerimasi calciocarbonatite consists principally of calcite together with lesser apatite, magnetite, and monticellite. Calcite hosts fluid and S-bearing Na–K–Ca-carbonate inclusions. Carbonatite melt and fluid inclusions occur in apatite and magnetite, and silicate melt inclusions in magnetite. This study presents statistically significant compositional data for quenched S- and P-bearing, Ca-alkali-rich carbonatite melt inclusions in magnetite and apatite. Magnetite-hosted silicate melts are peralkaline with normative sodium-metasilicate. On the basis of our microthermometric results on apatite-hosted melt inclusions and forsterite–monticellite phase relationships, temperatures of the early stage of magma evolution are estimated to be 900–1,000°C. At this time three immiscible liquid phases coexisted: (1) a Ca-rich, P-, S- and alkali-bearing carbonatite melt, (2) a Mg- and Fe-rich, peralkaline silicate melt, and (3) a C–O–H–S-alkali fluid. During the development of coexisting carbonatite and silicate melts, the Si/Al and Mg/Fe ratio of the silicate melt decreased with contemporaneous increase in alkalis due to olivine fractionation, whereas the alkali content of the carbonatite melt increased with concomitant decrease in CaO resulting from calcite fractionation. Overall the peralkalinity of the bulk composition of the immiscible melts increased, resulting in a decrease in the size of the miscibility gap in the pseudoquaternary system studied. Inclusion data indicate the formation of a carbonatite magma that is extremely enriched in alkalis with a composition similar to that of Oldoinyo Lengai natrocarbonatite. In contrast to the bulk compositions of calciocarbonatite rocks, the melt inclusions investigated contain significant amount of alkalis (Na2O + K2O) that is at least 5–10 wt%. The compositions of carbonatite melt inclusions are considered as being better representatives of parental magma composition than those of any bulk rock.  相似文献   

11.
Data obtained on lamprophyres from the carbonatite–volcanic unit in the lower horizon of the Tomtor Massif indicate that the rocks and zoned diopside and kaersutite phenocrysts in them are enriched in incompatible elements more significantly than is typical of alkaline ultramafic rocks of the Maymecha–Kotui and Kola provinces. The concentrations of these elements and their indicator ratios in the cores and intermediate zones of the diopside and kaersutite phenocrysts significantly vary, and this suggests that the minerals might have crystallized from different melts. This is consistent with the earlier conclusions, which were derived from studying melt inclusions, that the phenocrysts crystallized from mixing alkaline mafic melts of sodic and potassic types and different Mg–number which were enriched in the carbonatite component. The cores of the diopside phenocrysts started to crystallize from sodic mafic magma in a magmatic chamber, while the intermediate and outermost zones of this mineral crystallized from mixed sodic–potassic mafic melts. The carbonatite component was separated from the sodic mafic melt at high temperature (>1150°C) during diopside core crystallization. The bulk compositions of the alkaline lamprophyres and of the diopside and kaersutite phenocrysts contain lower normalized concentrations of HREE than LREE. This led us to conclude that the parental sodic and potassic mafic melts were derived from an enriched mantle source material under garnet–facies parameters, as is typical of continental rifts. It is noteworthy that the potassic mafic melt was derived at greater depths and lower degrees of melting of the mantle source than the sodic melt. The iron–rich sodic melt from which the cores of the diopside phenocrysts started to crystallize was enriched in V, REE, Y, and volatile components (H2O, CO2, F, Cl, and S). The onset of carbonate–silicate liquid immiscibility was marked by the redistribution of REE and Y into the carbonatite melt. The potassic, more Mg–rich mafic melt from which the intermediate and outermost zones of the diopside phenocrysts crystallized was enriched in Ti, Nb, Zr, and REE and always remained homogeneous when this mineral crystallized.  相似文献   

12.
Basaltic lavas form the isolated Quaternary volcanic centers of Diamond Craters and occur at Cow Lakes in S.E. Oregon. The exposed rocks are olivine and plagioclase phyric alkali olivine basalts. The holocrystalline groundmasses contain plagioclase, titanaugite, olivine, Fe-Ti oxides and minor apatite, and occur in the high-alumina (greater than 17%) petrographic province of the northwestern Great Basin.The whole rock and phenocryst compositions provide enough information to define the equilibrium state of the magmas. The solutions to the thermodynamic equations are valid for systems of known bulk composition and can be used to evaluate whether rock compositions are close to magma compositions. Two of the lavas from Diamond Craters have whole rock and phenocryst compositions consistent with their being natural melts. Rock compositions that reflect the effects of crystal separation (open systems) are recognized by significant differences in predicted versus observed phenocryst modes. The P-T conditions of phenocryst saturation and the crystallization history of the magmas can be inferred from petrologic data combined with thermodynamic modelling and mass balance constraints. The initial melts are inferred to have equilibrated at 0.8–1.0 GPa and 1210–1240°C. The majority of the lavas from Diamond Craters have compositions that reflect olivine and plagioclase crystal separation. These lavas can be related to two possible parent rock compositions by small amounts (2–8% by weight) of olivine and plagioclase separation.  相似文献   

13.
New data have been obtained on the distribution of the petrogenetic and rare-earth elements in the meimechite-series of rocks in Polar Siberia. It is shown that the meimechites, alkali picrites, and khatangites are comagmatic. The compositions of the primitive melts for the meimechite series have been estimated. It is suggested that the primary meimechite magmas were produced during the melting of lithosphere harzburgites that were enriched in incompatible elements due to infiltration of diapir melts with a low degree of partial melting.  相似文献   

14.
Tholeiites accompanying a majority of alkali basalts are restricted to the highly productive central part of the CECV plume activity in Vogelsberg and Hessian Depression. They mainly occur as quartz tholeiites which according to experiments of partial melting and material balances are products of olivine tholeiitic primary melts. The differentiation from olivine to quartz tholeiitic melts took place in lower crustal magma chambers where olivine tholeiitic melt intruded due to a density comparable with that of the country rocks. The fractionation due to separation of olivine and some clinopyroxene caused contamination of tholeiite magmas by tonalitic partial melts from the wall rocks of the magma chambers. The latter process is indicated by relatively high Rb, K and Pb and low Nb concentrations and by Nd, Sr and Pb isotopes. Contaminating crustal melts, which roughly attained a proportion of 10%, contained very low 143Nd/144Nd ratios from a Nd/Sm fractionation as old as 2.6 Ga. This is the first evidence from mafic rocks of this high age in the lower crust beneath Central Europe. Modelling with incompatible elements allows to recognize olivine tholeiites as products of about 1% partial melting of plume rocks consisting of 35% primitive and 65% depleted mantle materials. The production of tholeiites other than alkali basalts is restricted to the highest plume activity and the largest fraction of MORB type source rocks. Received: 10 December 1999 / Accepted: 23 June 2000  相似文献   

15.
In this paper, we discuss the formation conditions of rhyolites and results of their interaction with later portions of basic magmas on the basis of the investigation of melt and fluid inclusions in minerals from a rhyolite xenolith and host neovolcanic basalts of the Cleft segment of the Juan de Fuca Ridge. In terms of bulk chemistry and the compositions of melt inclusions in pyroxene and olivine phenocrysts, the basic rocks of the southern part of this segment are typical MOR basalts. Their olivine, clinopyroxene, and plagioclase crystallized at temperatures of 1160–1280°C and a pressure range between 20 and 100 MPa. The xenolith is a leucocratic rock with negligible amounts of mafic minerals, which clearly distinguishes it from the known occurrences of silicic rocks in the rift valleys of MOR. The rhyolite melt crystallized at temperatures of 900–880°C. The final stages of rhyolite melt crystallization at temperatures of 780–800°C were accompanied by the release of a saline aqueous fluid with high chloride contents. Based on the geochemical characteristics of melt inclusions and melting products, it can be suggested that the magmatic melt was produced by melting of metamorphosed oceanic crust within the Cleft segment under the influence sof saline aqueous fluid trapped in the pores and interstices of the rock. The rock represented by the xenolith is a late differentiation product of such melts. The ultimate products of silicic melt fractionation show high volatile contents: H2O > 3.0 wt %, Cl ～ 2.0 wt %, and F ～ 0.1 wt %. The interaction of the xenolith with the host basaltic melt occurred at temperatures equal or slightly higher than those of ferrobasalt melts (1190–1180°C). During ascent the xenolith occurred for a few tens of hours in high-temperature basic magma, and diffusion exchange between the basaltic and silicic melts was very minor.  相似文献   

16.
The compositions of parental melts of Tolbachinsky Dol (Kamchatka) basalts were estimated from the compositions of olivine-hosted (Fo90.5-83.1) primitive melt inclusions in the rocks of the Northern breakthrough of the Great Tolbachik Fissure Eruption (1975 A.C.) and of the late-Holocene cone “1004”. The parental melts contain 100–150 ppm Cu and 0.16–0.30 wt % S. These concentrations are much higher than those determined for the initial magmas of mid-ocean ridge basalts (MORB), for example of the Juan de Fuca ridge (Cu = 55–105 ppm, S=0.09–0.12 wt %). Modeling of mantle melting under variable redox conditions demonstrated that the high Cu and S contents in the Tolbachinsky Dol melts can be obtained by 6–12% melting of DMM-like source under oxidized conditions (ΔQFM = +1.2 ± 0.1) and do not require a significant (>30–35% for S) subduction-related influx of these elements to the mantle source. The high contents of Cu and S in the Tolbachinsky Dol melts are largely explained by the increase of sulfide solubility in a silicate melt under oxidized conditions. In contrast, relatively reduced (ΔQFM ～ 0) conditions of MORB generation result in low contents of Cu and S in their initial magmas. The estimated ΔQFM values agree well with the data obtained using the Cr-spinel–olivine oxybarometer. The high oxygen potential of Tolbachinsky Dol primary magmas is inherited by more evolved magmas, thus favouring Cu enrichment up to 270 ppm during magma fractionation, approaching maximum copper contents in the global systematics of island-arc rocks.  相似文献   

17.
A great volume of original information on the formation of the ultrabasic rocks of the Siberian Platform has been accumulated owing to the study of melt inclusions in Cr-spinels. The inclusions show the general tendencies in the behavior of the magmatic systems during the formation of the ultrabasic massifs of the Siberian Platform, tracing the main evolution trend of decreasing Mg number with SiO2 increase in the melts with subsequent transition from picrites through picrobasalts to basalts. The compositions of the melt inclusions indicate that the crystallization conditions of the rocks of the concentrically zoned massifs (Konder, Inagli, Chad) sharply differ from those of the Guli massif. Numerical modeling using the PETROLOG and PLUTON softwares and data on the composition of inclusions in Cr-spinels yielded maximum crystallization temperatures of the olivines from the dunites of the Konder (1545–1430°C), Inagli (1530–1430°C), Chad (1460–1420°C), and Guli (1520–1420°C) massifs, and those of Cr-spinels from the Konder (1420–1380°C), Inagli (up to 1430°C), Chad (1430–1330°C), and Guli (1410–1370°C) massifs. Modeling of the Guli massif with the PLUTON software using the compositions of the melt inclusions revealed the possible formation of the alkaline rocks at the final reverse stage of the evolution of the picritic magmas (with decrease of SiO2 and alkali accumulation) after termination of olivine crystallization with temperature decrease from 1240–1230°C to 1200–1090°C. Modeling with the PLUTON software showed that the dunites of the Guli massif coexisted with Fe-rich (with moderate TiO2 contents) melts, the crystallization of which led (beginning from 1210°C) to the formation of pyroxenes between cumulate olivine. Further temperature decrease (from 1125°C) with decreasing FeO and TiO2 contents provided the formation of clinopyroxenes of pyroxenites. For the Konder massif, modeling with the PLUTON software indicates the possible formation of kosvites from picrobasaltic magmas beginning from 1350°C and the formation of clinopyroxenites and olivine–diopside rocks from olivine basaltic melts from 1250°C.  相似文献   

18.
Here we combine petrological-geochemical and thermomechanical modeling techniques to explain origin of primary magmas of both Maimecha–Kotui meimechites and the Gudchikhinskaya basalts of Norilsk region, which represent, respectively, the end and the beginning of flood magmatism in the Siberian Trap Province.We have analyzed the least altered samples of meimechites, their olivine phenocrysts, and melt inclusions in olivines, as well as samples of dunites and their olivines, from boreholes G-1 and G-3 within the Guli volcanoplutonic complex in the Maimecha–Kotui igneous province of the northern Siberian platform. The Mn/Fe and Ni/MgO ratios in olivines indicate a mantle peridotite source of meimechites. Meimechite parental magma that rose to shallow depths was rich in alkalis and highly magnesian (24 wt.% MgO), largely degassed, undersaturated by sulfide liquid and oxidized. At greater depths, it was, likely, high in CO2 (6 wt.%) and H2O (2 wt.%) and resulted from partial melting of initially highly depleted and later metasomatized harzburgite some 200 km below the surface. Trace-element abundances in primary meimechite magma suggest presence of garnet and K-clinopyroxene, in the mantle source and imply for genetic link to the sources of the early Siberian flood basalts (Gudchikhinskaya suite) and kimberlites. The analyzed dunite samples from the Guli complex have chemistry and mineralogy indicating their close relation to meimechites.We have also computed thermomechanical model of interaction of a hot mantle plume with the shield lithosphere of variable thickness, using realistic temperature- and stress-dependent visco-elasto-plastic rocks rheology and advanced finite element solution technique.Based on our experimental and modeling results we propose that a Permian–Triassic plume, with potential temperature of about 1650 °C transported a large amount of recycled ancient oceanic crust (up to 15%) as SiO2-supersaturated carbonated eclogite. Low-degree partial melting of eclogite at depths of 250–300 km produced carbonate-silicate melt that metasomatized the lithospheric roots of the Siberian shield. Further rise of the plume under relatively attenuated lithosphere (Norilsk area) led to progressive melting of eclogite and formation of reaction pyroxenite, which then melted at depths of 130–180 km. Consequantly, a large volume of melt (Gudchikhinskaya suite) penetrated into the lithosphere and caused its destabilization and delamination. Delaminated lithosphere that included fragments of locally metasomatized depleted harzburgite subsided into the plume and was heated to the temperatures of the plume interior with subsequent generation of meimechite magma. Meimechites showed up at the surface only under thicker part of the lithosphere aside from major melting zone above because otherwise they were mixed up in more voluminous flood basalts. We further suggest that meimechites, uncontaminated Siberian flood basalts and kimberlites all shear the same source of strongly incompatible elements, the carbonated recycled oceanic crust carried up by hot mantle plume.  相似文献   

19.
Partial melting has been shown to be an important mechanism for intracrustal differentiation and granite petrogenesis. However, a series of compositional differences between granitic melt from experiments and natural granites indicate that the processes of crustal differentiation are complex. To shed light on factors that control the processes of crustal differentiation, and then the compositions of granitic magma, a combined study of petrology and geochemistry was carried out for granites (in the forms of granitic veins and parautochthonous granite) from a granulite terrane in the Tongbai orogen, China. These granites are characterized by high SiO2 (>72 wt%) and low FeO and MgO (<4 wt%) with low Na2O/K2O ratios (<0.7). Minerals in these granites show variable microstructures and compositions. Phase equilibrium modelling using P–T pseudosections shows that neither anatectic melts nor fractionated melts match the compositions of the target granites, challenging the conventional paradigm that granites are the crystallized product of pure granitic melts. Based on the microstructural features of minerals in the granites, and a comparison of their compositions with crystallized minerals from anatectic melts and minerals in granulites, the minerals in these granitoids are considered to have three origins. The first is entrained garnets, which show comparable compositions with those in host granulites. The second is early crystallized mineral from melts, which include large plagioclase and K-feldspar (with high Ca contents) crystals as well as a part of biotite whose compositions can be reproduced by crystallization of the anatectic melts. The compositions of other minerals such as small grained plagioclase, K-feldspar and anorthoclase in the granites with low Ca contents are not well reconstructed, so they are considered as the third origin of crystallized products of fractionated melts. The results of mass balance calculation show that the compositions of these granites can be produced by mixing between different proportions of crystallized minerals and fractionated melts with variable amounts of entrained minerals. However, the calculated modal proportions of different crystallized minerals (plagioclase, K-feldspar, biotite and quartz) in the granites are significantly different from those predicted by melt crystallization modelling. Specifically, some rocks have lower modes of biotite and plagioclase, whereas others show lower K-feldspar modes than those produced by melt crystallization. This indicates that the crystallized minerals would be differentially separated from the primary magmas to form the evolved magmas that produce these granites. Therefore, the crystal entrainment and differential melt-crystal separation make important contributions to the composition of the target granites. Compared with leucogranites worldwide, the target granites show comparable compositions. As such, the leucogranites may form through the crystal fractionation of primary granitic magmas at different extents in addition to variable degrees of partial melting.  相似文献   

20.
The genesis of basaltic magmas   总被引：29，自引：2，他引：29  
This paper reports the results of a detailed experimental investigation of fractionation of natural basaltic compositions under conditions of high pressure and high temperature. A single stage, piston-cylinder apparatus has been used in the pressure range up to 27 kb and at temperatures up to 1500° C to study the melting behaviour of several basaltic compositions. The compositions chosen are olivine-rich (20% or more normative olivine) and include olivine tholeiite (12% normative hypersthene), olivine basalt (1% normative hypersthene) alkali olivine basalt (2% normative nepheline) and picrite (3% normative hypersthene). The liquidus phases of the olivine tholeiite and olivine basalt are olivine at 1 Atmosphere, 4.5 kb and 9 kb, orthopyroxene at 13.5 and 18 kb, clinopyroxene at 22.5 kb and garnet at 27 kb. In the alkali olivine basalt composition, the liquidus phases are olivine at 1 Atmosphere and 9 kb, orthopyroxene with clinopyroxene at 13.5 kb, clinopyroxene at 18 kb and garnet at 27 kb. The sequence of appearance of phases below the liquidus has also been studied in detail. The electron probe micro-analyser has been used to make partial quantitative analyses of olivines, orthopyroxenes, clinopyroxenes and garnets which have crystallized at high pressure.These experimental and analytical results are used to determine the directions of fractionation of basaltic magmas during crystallization over a wide range of pressures. At pressures corresponding to depths of 35–70 km separation of aluminous enstatite from olivine tholeiite magma produces a direct fractionation trend from olivine tholeiites through olivine basalts to alkali olivine basalts. Co-precipitation of sub-calcic, aluminous clinopyroxene with the orthopyroxene in the more undersaturated compositions of this sequence produces derivative liquids of basanite type. Magmas of alkali olivine basalt and basanite type represent the lower temperature liquids derived by approximately 30% crystallization of olivine-rich tholeiite at 35–70 km depth. At depths of about 30 km, fractionation of olivine-rich tholeiite with separation of both olivine and low-alumina enstatite, joined at lower temperatures by sub-calcic clinopyroxene, leads to derivative liquids with relatively constant SiO2 (48 to 50%) increasingly high Al2O3 (15–17%) contents and retaining olivine + hypersthene normative chemistry (5–15% normative olivine). These have the composition of typical high-alumina olivine tholeiites. The effects of low pressure fractionation may be superimposed on magma compositions derived from various depths within the mantle. These lead to divergence of the alkali olivine basalt and tholeiitic series but convergence of both the low-alumina and high-alumina tholeiites towards quartz tholeiite derivative liquids.The general problem of derivation of basaltic magmas from a mantle of peridotitic composition is discussed in some detail. Magmas are considered to be a consequence of partial melting but the composition of a magma is determined not by the depth of partial melting but by the depth at which magma segregation from residual crystals occurs. Magma generation from parental peridotite (pyrolite) at depths up to 100 km involves liquid-crystal equilibria between basaltic liquids and olivine + aluminous pyroxenes and does not involve garnet. At 35–70 km depth, basaltic liquids segregating from a pyrolite mantle will be of alkali olivine basalt type with about 20% partial melting but with increasing degrees of partial melting, liquids will change to olivine-rich tholeiite type with about 30% melting. If the depth of magma segregation is about 30 km, then magmas produced by 20–25% partial melting will be of high-alumina olivine tholeiite type, similar to the oceanic tholeiites occurring on the sea floor along the mid-oceanic ridges.Hypotheses of magma fractionation and generation by partial melting are considered in relation to the abundances and ratios of trace elements and in relation to isotopic abundance data on natural basalts. It is shown that there is a group of elements (including K, Ti, P, U, Th, Ba, Rb, Sr, Cs, Zr, Hf and the rare-earth elements) which show enrichment factors in alkali olivine basalts and in some tholeiites, which are inconsistent with simple crystal fractionation relationships between the magma types. This group of elements has been called incompatible elements referring to their inability to substitute to any appreciable extent in the major minerals of the upper mantle (olivine, aluminous pyroxenes). Because of the lack of temperature contrast between magma and wall-rock for a body of magma near to its depth of segregation in the mantle, cooling of the magma involves complementary processes of reaction with the wall-rook, including selective melting and extraction of the lowest melting fraction. The incompatible elements are probably highly concentrated in the lowest melting fraction of the pyrolite. The production of large overall enrichments in incompatible elements in a magma by reaction with and highly selective sampling of large volumes of mantle wall-rock during slow ascent of a magma is considered to be a normal, complementary process to crystal fractionation in the mantle. This process has been called wall-rock reaction. Magma generation in the mantle is rarely a simple, closed-system partial melting process and the isotopic abundances and incompatible element abundances of a basalt as observed at the earth's surface may be largely determined by the degree of reaction with the mantle or lower crustal wall-rocks and bear little relation to the abundances and ratios of the original parental mantle material (pyrolite).Occurrences of cognate xenoliths and xenocrysts in basalts are considered in relation to the experimental data on liquid-crystal equilibria at high pressure. It is inferred that the lherzolite nodules largely represent residual material after extraction of alkali olivine basalt from mantle pyrolite or pyrolite which has been selectively depleted in incompatible elements by wall-rock reaction processes. Lherzolite nodules included in tholeiitic magmas would melt to a relatively large extent and disintegrate, but would have a largely refractory character if included in alkali olivine basalt magma. Other examples of xenocrystal material in basalts are shown to be probable liquidus crystals or accumulates at high pressure from basaltic magma and provide a useful link between the experimental study and natural processes.  相似文献   

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