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1.
Mt. Baker is a dominantly andesitic stratovolcano in the northern Cascade arc. In this study, we show that the andesites are not all derived from similar sources, and that open-system processes were dominant during their petrogenesis. To this end, we discuss petrographic observations, mineral chemistry, and whole rock major and trace element chemistry for three of Mt. Baker’s late Pleistocene to Holocene lava flow units. These include the basalt and basaltic andesite of Sulphur Creek (SC) (51.4–55.8 wt% SiO2, Mg# 57–58), the Mg-rich andesite of Glacier Creek (GC) (58.3–58.7 wt% SiO2, Mg# 63–64), and the andesite and dacite of Boulder Glacier (BG) (60.2–64.2 wt% SiO2, Mg# 50–57). Phenocryst populations in all units display varying degrees of reaction and disequilibrium textures along with complicated zoning patterns indicative of open-system processes. All lavas are medium-K and calc-alkaline, but each unit displays distinctive trace element and REE characteristics that do not correlate with the average SiO2 content of the unit. The mafic lavas of SC have relatively elevated REE abundances with the lowest (La/Yb)N (~4.5). The intermediate GC andesites (Mg- and Ni-rich) have the lowest REE abundances and the highest (La/Yb)N (~6.7) with strongly depleted HREE. The more felsic BG lavas have intermediate REE abundances and (La/Yb)N (~6.4). The high-Mg character of the GC andesites can be explained by addition of 4% of a xenocrystic olivine component. However, their depleted REE patterns are similar to other high-Mg andesites reported from Mt. Baker and require a distinct mantle source. The two dominantly andesitic units (GC and BG) are different enough from each other that they could not have been derived from the same parent basalt. Nor could either of them have been derived from the SC basalt by crystal fractionation processes. Crystal fractionation also cannot explain the compositional diversity within each unit. Compositional diversity within the SC unit (basalt to basaltic andesite) can, however, be successfully modeled by mixing of basalt with compositions similar to the dacites in the BG unit. Given that the BG dacites erupted at ~80–90 ka, and a similar composition was mixed with the SC lavas at 9.8 ka, the process that produced this felsic end-member must have been repeatedly active for at least 70 ka.  相似文献   

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

3.
Unusually magnesian (Mg# ∼76) basalts have been sampled from a small submarine volcano situated on the Mariana arc magmatic front. Total alkalis range from 1.7 to 1.94%, Al2O3 from 9.09 to 10.3% and CaO from 13.9 to 14.09%. These lavas can be classified based on mineralogy as picrite and ankaramite. Olivine-hosted melt inclusions (MIs) have median MgO contents of 17.17–17.86 wt%, 0.35–0.5% TiO2, 42–50% SiO2 and 1.66–3.43% total alkalis, which suggest that the parental magmas were primitive mantle melts. Trace element concentrations for both MIs and lavas are arc-like, although more depleted than most arc lavas. Chlorine (182–334 ppm) and H2O contents (0.11–0.64 wt%) in the MIs are consistent with the estimated median oxygen fugacities (log ΔFMQ of + 1.53–1.66) which lie at the low end of the range estimates for arc basalts and picrites (ΔFMQ = + 1 to + 3). Isotopic compositions of Sr, Nd, Hf and Pb are similar to those of other Mariana arc lavas and indicate derivation from an Indian Ocean mantle domain. The averaged magmatic temperature estimate from several geothermometers was 1,367°C at 1–1.5 GPa. We propose that high-Mg magmagenesis in this region results from the adiabatic decompression melting of relatively anhydrous but metasomatized mantle wedge. This melting is attributed to enhanced upwelling related to unusual tectonics on the over-riding plate related to a tear or other discontinuity on the subducted slab.Electronic Supplementary Material Supplementary material is available for this article at and is accessible for authorized users.  相似文献   

4.
High-Mg basaltic andesites and andesites occur in the central trans-Mexican volcanic belt, and their primitive geochemical characteristics suggest equilibration with mantle peridotite. These lavas may represent slab melts that reequilibrated with overlying peridotite or hydrous partial melts of a peridotite source. Here, we experimentally map the liquidus mineralogy for a high-Mg basaltic andesite (9.6 wt% MgO, 54.4 wt% SiO2, Mg# = 75.3) as a function of temperature and H2O content over a range of mantle wedge pressures. Our results permit equilibration of this composition with a harzburgite residue at relatively high water contents (>7 wt%) and low temperatures (1,080–1,150°C) at 11–14 kbar. However, in contrast to the high Ni contents characteristic of olivine phenocrysts in many such samples from central Mexico, those of olivine phenocrysts in our sample are more typical of mantle melts that have fractionated a small amount of olivine. To account for this and the possibility that the refractory mantle source may have had olivine more Fo-rich than Fo90, we numerically evaluated alternative equilibration conditions, using our starting bulk composition adjusted to be in equilibrium with Fo92 olivine. This shifts equilibration conditions to higher temperatures (1,180–1,250°C) at mantle wedge pressures (11–15 kbar) for H2O contents (>3 wt%) comparable to those analyzed in olivine-hosted melt inclusions from this region. Comparison with geodynamic models shows that final equilibration occurred shallower than the peak temperature of the mantle wedge, suggesting that basaltic melts from the hottest part of the wedge reequilibrated with shallower mantle as they approached the Moho.  相似文献   

5.
The origin of compositional heterogeneities among the magmas parental to mid-ocean ridge basalts (MORB) was investigated using a single rock piece of the olivine-phyric basalt from 43°N, Mid-Atlantic Ridge (AII D11-177). The exceptional feature of this sample is presence of very primitive olivine crystals (90–91 mol% Fo) that are significantly variable in terms of CaO (0.15–0.35 wt%). A population of low-Ca olivine (0.15–0.25 wt% CaO) is also notably distinct from high-Ca olivine population in AII D11-177, and primitive MORB olivine in general, in having unusual assemblage of trapped mineral and glass inclusions. Mineral inclusions are represented by high-magnesian (Mg# 90.7–91.1 mol%) orthopyroxene and Cr-spinel, distinctly enriched in TiO2 (up to 5 wt%, c.f. <1 wt% in common MORB spinel). Glass inclusions associated with orthopyroxene and high-Ti Cr-spinel have andesitic compositions (53–58 wt% SiO2). Compared to the pillow-rim glass and “normal” MORB inclusions, the Si-rich glass inclusions in low-Ca olivine have strongly reduced Ca and elevated concentrations of Ti, Na, K, P, Cl, and highly incompatible trace elements. Strong variability is recorded among glass inclusions within a single olivine phenocrysts. We argue that the observed compositional anomalies are mineralogically controlled, and thus may arise from the interaction between hot MORB magmas and crystal cumulates in the oceanic crust or magma chamber.  相似文献   

6.
The Edgecumbe volcanic field is a Holocene volcanic province located on Kruzof Island, SE Alaska. Exposed within the 260 km2 field are basalt, andesitic basalt, andesite, dacite and rhyodacite. The rhyodacites were erupted after the basalts and before the andesites. The volcanics, which are Al-rich (14–18 wt%) and lack an iron enrichment trend, range from tholeiites (47 wt% SiO2) through rhyodacites (72%), but a compositional gap of approximately 9 wt% separates the dacites and rhyodacites. Initial 87Sr/86Sr ranges from 0.70297 in the basalts to 0.70440 in a pyroxene andesite. δ 18O increases across the suite: 5.8‰ to 7.9‰. Plagioclase (An32–86) is the dominant phenocryst in all but one lava. Olivine (Fo58–86) occurs in the basic lavas (<53 wt% SiO2), but is replaced by orthopyroxene (En43–73) and clinopyroxene (En31Wo41-En48Wo40) in the more siliceous volcanics. In the basalts and rhyodacites, plagioclase is weakly zoned, but extreme zoning (<30 mole% An) is characteristic of phenocrysts in the intermediate lavas. Fractionation of the observed phenocryst assemblages could not have produced the more silicous volcanics. Instead they were generated by partial melting of intrusive basement (87Sr/86Sr=0.70487; δ 18O: 8.7–9.3) by basaltic magma and subsequent assimilation. Mass balance calculations show the rhyodacites are almost pure partial melt (<5% basaltic component) whereas the intermediate lavas contain between 30 and 60% partial melt.  相似文献   

7.
This paper characterizes late Holocene basalts and basaltic andesites at Medicine Lake volcano that contain high pre-eruptive H2O contents inherited from a subduction related hydrous component in the mantle. The basaltic andesite of Paint Pot Crater and the compositionally zoned basaltic to andesitic lavas of the Callahan flow erupted approximately 1000 14C years Before Present (14C years b.p.). Petrologic, geochemical and isotopic evidence indicates that this late Holocene mafic magmatism was characterized by H2O contents of 3 to 6 wt% H2O and elevated abundances of large ion lithophile elements (LILE). These hydrous mafic inputs contrast with the preceding episodes of mafic magmatism (from 10,600 to ∼3000 14C years b.p.) that was characterized by the eruption of primitive high alumina olivine tholeiite (HAOT) with low H2O (<0.2 wt%), lower LILE abundance and different isotopic characteristics. Thus, the mantle-derived inputs into the Medicine Lake system have not always been low H2O, primitive HAOT, but have alternated between HAOT and hydrous subduction related, calc-alkaline basalt. This influx of hydrous mafic magma coincides temporally and spatially with rhyolite eruption at Glass Mountain and Little Glass Mountain. The rhyolites contain quenched magmatic inclusions similar in character to the mafic lavas at Callahan and Paint Pot Crater. The influence of H2O on fractional crystallization of hydrous mafic magma and melting of pre-existing granite crust beneath the volcano combined to produce the rhyolite. Fractionation under hydrous conditions at upper crustal pressures leads to the early crystallization of Fe-Mg silicates and the suppression of plagioclase as an early crystallizing phase. In addition, H2O lowers the saturation temperature of Fe and Mg silicates, and brings the temperature of oxide crystallization closer to the liquidus. These combined effects generate SiO2-enrichment that leads to rhyodacitic differentiated lavas. In contrast, low H2O HAOT magmas at Medicine Lake differentiate to iron-rich basaltic liquids. When these Fe-enriched basalts mix with melted granitic crust, the result is an andesitic magma. Since mid-Holocene time, mafic volcanism has been dominated primarily by hydrous basaltic andesite and andesite at Medicine Lake Volcano. However, during the late Holocene, H2O-poor mafic magmas continued to be erupted along with hydrous mafic magmas, although in significantly smaller volumes. Received: 4 January 1999 / Accepted: 30 August 1999  相似文献   

8.
Near-liquidus crystallization experiments have been carried out on two basalts (12.5 and 7.8 wt% MgO) from Soufriere, St Vincent (Lesser Antilles arc) to document the early stages of differentiation in calc-alkaline magmas. The water-undersaturated experiments were performed mostly at 4 kbar, with 1.6 to 7.7 wt% H2O in the melt, and under oxidizing conditions (ΔNNO = −0.8 to +2.4). A few 10 kbar experiments were also performed. Early differentiation of primitive, hydrous, high-magnesia basalts (HMB) is controlled by ol + cpx + sp fractionation. Residual melts of typical high-alumina basalt (HAB) composition are obtained after 30–40% crystallization. The role of H2O in depressing plagioclase crystallization leads to a direct relation between the Al2O3 content of the residual melt and its H2O concentration, calibrated as a geohygrometer. The most primitive phenocryst assemblage in the Soufriere suite (Fo89.6 olivine, Mg-, Al- and Ti-rich clinopyroxene, Cr–Al spinel) crystallized from near-primary (Mg# = 73.5), hydrous (∼5 wt% H2O) and very oxidized (ΔNNO = +1.5–2.0) HMB liquids at middle crustal pressures and temperatures from ∼1,160 to ∼1,060°C. Hornblende played no role in the early petrogenetic evolution. Derivative HAB melts may contain up to 7–8 wt% dissolved H2O. Primitive basaltic liquids at Soufriere, St Vincent, have a wide range of H2O concentrations (2–5 wt%).  相似文献   

9.
Silicic volcanic deposits (>65 wt% SiO2), which occur as domes, lavas and pyroclastic deposits, are relatively abundant in the Macolod Corridor, SW Luzon, Philippines. At Makiling stratovolcano, silicic domes occur along the margins of the volcano and are chemically similar to the silicic lavas that comprise part of the volcano. Pyroclastic flows are associated with the Laguna de Bay Caldera and these are chemically distinct from the domes and lavas at Makiling stratovolcano. As a whole, samples from the Laguna de Bay Caldera contain lower concentrations of MgO and higher concentrations of Fe2O3(t) than the samples from domes and lavas. The Laguna de Bay samples are more enriched in incompatible trace elements. The silicic rocks from the domes, Makiling Volcano and Laguna de Bay Caldera all contain high alkalis and high K2O/Na2O ratios. Melting experiments of primitive basalts and andesites demonstrate that it is difficult to produce high K2O/Na2O silicic magmas by fractional crystallization or partial melting of a low K2O/Na2O source. However, recent melting experiments (Sisson et al., Contrib Mineral Petrol 148:635–661, 2005) demonstrate that extreme fractional crystallization or partial melting of K-rich basalts can produce these silicic magmas. Our model for the generation of the silicic magmas in the Macolod Corridor requires partial melting of mantle-derived, evolved, moderate to K-rich, crystallized calc-alkaline magmas that ponded and crystallized in the mid-crust. Major and trace element variations, along with oxygen isotopes and ages of the deposits, are consistent with this model. Electronic Supplementary Material Supplementary material is available for this article at  相似文献   

10.
Primitive chemical characteristics of high-Mg andesites (HMA) suggest equilibration with mantle wedge peridotite, and they may form through either shallow, wet partial melting of the mantle or re-equilibration of slab melts migrating through the wedge. We have re-examined a well-studied example of HMA from near Mt. Shasta, CA, because petrographic evidence for magma mixing has stimulated a recent debate over whether HMA magmas have a mantle origin. We examined naturally quenched, glassy, olivine-hosted (Fo87–94) melt inclusions from this locality and analyzed the samples by FTIR, LA-ICPMS, and electron probe. Compositions (uncorrected for post-entrapment modification) are highly variable and can be divided into high-CaO (>10 wt%) melts only found in Fo > 91 olivines and low-CaO (<10 wt%) melts in Fo 87–94 olivine hosts. There is evidence for extensive post-entrapment modification in many inclusions. High-CaO inclusions experienced 1.4–3.5 wt% FeOT loss through diffusive re-equilibration with the host olivine and 13–28 wt% post-entrapment olivine crystallization. Low-CaO inclusions experienced 1–16 wt% olivine crystallization with <2 wt% FeOT loss experienced by inclusions in Fo > 90 olivines. Restored low-CaO melt inclusions are HMAs (57–61 wt% SiO2; 4.9–10.9 wt% MgO), whereas high-CaO inclusions are primitive basaltic andesites (PBA) (51–56 wt% SiO2; 9.8–15.1 wt% MgO). HMA and PBA inclusions have distinct trace element characteristics. Importantly, both types of inclusions are volatile-rich, with maximum values in HMA and PBA melt inclusions of 3.5 and 5.6 wt% H2O, 830 and 2,900 ppm S, 1,590 and 2,580 ppm Cl, and 500 and 820 ppm CO2, respectively. PBA melts are comparable to experimental hydrous melts in equilibrium with harzburgite. Two-component mixing between PBA and dacitic magma (59:41) is able to produce a primitive HMA composition, but the predicted mixture shows some small but significant major and trace element discrepancies from published whole-rock analyses from the Shasta locality. An alternative model that involves incorporation of xenocrysts (high-Mg olivine from PBA and pyroxenes from dacite) into a primary (mantle-derived) HMA magma can explain the phenocryst and melt inclusion compositions but is difficult to evaluate quantitatively because of the complex crystal populations. Our results suggest that a spectrum of mantle-derived melts, including both PBA and HMA, may be produced beneath the Shasta region. Compositional similarities between Shasta parental melts and boninites imply similar magma generation processes related to the presence of refractory harzburgite in the shallow mantle.  相似文献   

11.
We report the oxygen isotope composition of olivine and orthopyroxene phenocrysts in lavas from the main magma types at Mt Shasta and Medicine Lake Volcanoes: primitive high-alumina olivine tholeiite (HAOT), basaltic andesites (BA), primitive magnesian andesites (PMA), and dacites. The most primitive HAOT (MgO > 9 wt%) from Mt. Shasta has olivine δ18O (δ18OOl) values of 5.9–6.1‰, which are about 1‰ higher than those observed in olivine from normal mantle-derived magmas. In contrast, HAOT lavas from Medicine Lake have δ18OOl values ranging from 4.7 to 5.5‰, which are similar to or lower than values for olivine in equilibrium with mantle-derived magmas. Other magma types from both volcanoes show intermediate δ18OOl values. The oxygen isotope composition of the most magnesian lavas cannot be explained by crustal contamination and the trace element composition of olivine phenocrysts precludes a pyroxenitic mantle source. Therefore, the high and variable δ18OOl signature of the most magnesian samples studied (HAOT and BA) comes from the peridotitic mantle wedge itself. As HAOT magma is generated by anhydrous adiabatic partial melting of the shallow mantle, its 1.4‰ range in δ18OOl reflects a heterogeneous composition of the shallow mantle source that has been influenced by subduction fluids and/or melts sometime in the past. Magmas generated in the mantle wedge by flux melting due to modern subduction fluids, as exemplified by BA and probably PMA, display more homogeneous composition with only 0.5‰ variation. The high-δ18O values observed in magnesian lavas, and principally in the HAOT, are difficult to explain by a single-stage flux-melting process in the mantle wedge above the modern subduction zone and require a mantle source enriched in 18O. It is here explained by flow of older, pre-enriched portions of the mantle through the slab window beneath the South Cascades.  相似文献   

12.
The Valley of Mexico and surrounding regions of Mexico and Morelos states in central Mexico contain more than 250 Quaternary eruptive vents in addition to the large, composite volcanoes of Popocatépetl, Iztaccíhuatl, and Nevado de Toluca. The eruptive vents include cinder and lava cones, shield volcanoes, and isolated andesitic and dacitic lava flows, and are most numerous in the Sierra Chichináutzin that forms the southern terminus of the Valley of Mexico. The Chichináutzin volcanic field (CVF) is part of the E-W-trending Mexican Volcanic Belt (MVB), a subduction-related volcanic arc that extends across Mexico. The crustal thickness beneath the CVF (∼50 km) is the greatest of any region in the MVB and one of the greatest found in any arc worldwide. Lavas and scoriae erupted from vents in the CVF include alkaline basalts and calc-alkaline basaltic andesites, andesites, and dacites. Both alkaline and calc-alkaline groups contain primitive varieties that have whole rock Mg#, MgO, and Ni contents, and liquidus olivine compositions (≤Fo90) that are close to those expected of partial melts from mantle peridotite. Primitive varieties also show a wide range of incompatible trace element abundances (e.g. Ba 210–1080 ppm; Ce 25–100 ppm; Zr 130–280 ppm). Data for primitive calc-alkaline rocks from both the CVF and other regions of the MVB to the west are consistent with magma generation in an underlying mantle wedge that is depleted in Ti, Zr, and Nb and enriched in large ion lithophile (K, Ba, Rb) and light rare earth (La, Ce) elements. Extents of partial melting estimated from Ti and Zr data are lower for primitive calc-alkaline magmas in the CVF than for those from the regions of the MVB to the west where the crust is thinner. The distinctive major element compositions (low CaO and Al2O3, high SiO2) of the primitive calc-alkaline magmas in the CVF indicate a more refractory mantle source beneath this region of thick crust. In contrast, primitive alkaline magmas from the CVF and other regions of the MVB show compositional similarities to intraplate-type alkali basalts erupted behind the arc in the Mexican Basin and Range province. These similarities are consistent with the hypothesis that slab-induced convection in the mantle wedge beneath the MVB causes advection of asthenospheric mantle from behind the arc to the region of magma generation. Trace element systematics of primitive magmas in the MVB reveal substantial variability in both the extent of mantle wedge enrichment by subduction processes and in the composition of mantle heterogeneities that are related to previous extraction of alkaline to sub-alkaline basaltic melts. Received: 23 June 1998 / Accepted: 23 December 1998  相似文献   

13.
The bulk (post-eruptive) wt% FeO concentration in each of 11 phenocryst-poor (<5%) andesite and dacite (60–69 wt% SiO2) lavas from different monogenetic vents in the Mexican arc has been measured by titration, in duplicate. The results match, within analytical error, the wt% FeO content of the magmas during phenocryst growth (pre-euptive), which were calculated on the basis of oxygen fugacity and temperature results from Fe–Ti two-oxide oxygen barometry. The average deviation between the pre- and post-eruptive FeO concentrations is ±0.15 wt%. Application of the plagioclase-liquid hygrometer shows that at the time of phenocryst growth, these 11 magmas contained from ~3–8 wt% H2O, which was extensively degassed upon eruption. There is no evidence that degassing of ≤8 wt% H2O changed the oxidation state of these magmas. Calculations of pre-eruptive and post-eruptive oxygen fugacity values relative to the Ni-NiO buffer (in terms of log10 units) for the 11 samples span a similar range; pre-eruptive ∆NNO = −0.9 to +0.7 and post-eruptive ∆NNO = −0.4 to +0.8. The data further show that extensive groundmass (closed-system) crystallization had no affect on bulk Fe3+/Fe2+ ratios. Finally, there is no systematic variation in the range of pre-eruptive Fe3+/FeT values of the samples as a function of SiO2 concentration (i.e., differentiation). Therefore, the results of this study indicate that the elevated Fe3+/FeT ratios of arc andesites and dacites, compared with magmas erupted in other tectonic settings, cannot be attributed to the effects of (1) degassing of H2O, (2) closed-system crystallization, and/or (3) differentiation effects, but instead must be inherited from their parental source rocks (i.e., mantle-derived arc basalts).  相似文献   

14.
The lava sequence of the central-western Deccan Traps (from Jalgaon towards Mumbai) is formed by basalts and basaltic andesites having a significant variation in TiO2 (from 1.2 to 3.3 wt%), Zr (from 84 to 253 ppm), Nb (from 5 to 16ppm) and Ba (from 63 to 407 ppm), at MgO ranging from 10 to 4.2 wt%. Most of these basalts follow a liquid line of descent dominated by low pressure fractionation of clinopyroxene, plagioclase and olivine, starting from the most mafic compositions, in a temperature range from 1220° to 1125°C. These rocks resemble those belonging to the lower-most formations of the Deccan Traps in the Western Ghats (Jawhar, Igatpuri and Thakurvadi) as well as those of the Poladpur formation. Samples analyzed for87Sr/86Sr give a range of initial ratios from 0.70558 to 0.70621. A group of flows of the Dhule area has low TiO2 (1.2–1.5 wt%) and Zr (84–105 ppm) at moderate MgO (5.2–6.2 wt%), matching the composition of low-Ti basalts of Gujarat, low-Ti dykes of the Tapti swarm and Toranmal basalts, just north of the study area. This allows chemical correlations between the lavas of central Deccan, the Tapti dykes and the north-western outcrops. The mildly enriched high field strength element contents of the samples with TiO2 > 1.5 wt% make them products of mantle sources broadly similar to those which generated the Ambenali basalts, but their high La/Nb and Ba/Nb, negative Nb anomalies in the mantle normalized diagrams, and relatively high87Sr/86Sr, make evident a crustal input with crustally derived materials at less differentiated stages than those represented in this sample set, or even within the sub-Indian lithospheric mantle.  相似文献   

15.
 This paper uses the geochemistry of primitive mafic lavas from the Rungwe volcanic province (southwestern Tanzania) to infer the source mineralogy and melting history. Post-Miocene mafic lavas from Rungwe include alkali basalts, basanites, nephelinites and picrites with up to 18.9 wt% MgO; nephelinites (>13.5% normative nepheline) are restricted to Kiejo volcano in the southern portion of the province. Rungwe lavas differ from most Western Rift volcanics in that they are not unusually potassic (K2O/Na2O ca. 0.40). Sparsely phyric mafic lavas contain phenocrysts and xenocrysts of plagioclase (An82–90), clinopyroxene (4.5–9.5 wt% Al2O3), and olivine (Fo79–88); one basanite contains a 1 mm xenocryst of apatite included in magnesian clinopyroxene. All samples have high abundances of incompatible elements (e.g., 0.7–2.2 wt% P2O5) and are enriched in REE relative to HFSE (Hf, Zr, Ti, Y), Cs, Ba, and K. Some incompatible element ratios are constant throughout the Rungwe suite (e.g., Zr/Nb, Sr/Ce, K/Rb), but other ratios are extremely variable and exceed the range measured in global Ocean Island Basalts (OIB) (e.g., Ba/Nb, Sm/Zr, La/Nb, Pb/Ce, Nb/U). The range in degree of silica saturation, and its excellent correlation with P2O5/Al2O3, indicate that the Rungwe suite records variable degrees of melting. Variations of individual incompatible trace element abundances in nephelinite and basanite samples suggest that the source contains metasomatic amphibole, ilmenite, apatite, and zircon. The Rungwe suite is interpreted as a series of low-percentage melts of CO2-rich peridotite at pressures that span the garnet-spinel transition. A geochemical comparison of Rungwe samples to lavas from other Western Rift volcanic centers requires that the source mineralogy varies along the rift axis, although each province is underlain by metasomatized peridotite. The incompatible trace element signatures of Western Rift lavas indicate that the source area is typically homogeneous on the scale of individual volcanoes, although lavas from each volcano reflect a range in degree of melting. Significantly, volcanoes with distinct geochemistry are always separated by major rift faults, suggesting that volcanic and tectonic surface features may correspond to metasomatic provinces within the subcontinental lithospheric mantle. Received: 30 May 1994 / Accepted: 5 April 1995  相似文献   

16.
We have conducted high pressure (to 3 kbar), water saturated melting experiments on an andesite (62 wt% SiO2) and a basaltic andesite (55 wt% SiO2) from western Mexico. A close comparison between the experimental phase assemblages and their compositions, and the phenocryst assemblages of the lavas, is found in water saturated liquids, suggesting that the CO2 content was minimal in the fluid phase. Thus the historic lavas from Volcan Colima (with phenocrysts of orthopyroxene, augite, plagioclase, and hornblende) were stored at a temperature between 950–975 °C, at a pressure between 700–1500 bars, and with a water content of 3.0–5.0 wt%. A hornblende andesite (spessartite) from Mascota, of nearly identical composition but with only amphibole phenocrysts, had a similar temperature but equilibrated at a minimum of 2000 bars pressure with a dissolved water content of at least 5.5 wt% in the liquid. Experiments on the basaltic andesite show that the most common natural phenocryst assemblages (olivine, ±augite, ±plagioclase) could have precipitated at temperatures from 1000–1150 °C, in liquids with a wide range of dissolved water content (∼2.0–6.0 wt%) and a corresponding pressure range. A lava of the same bulk composition with phenocrysts of hornblende, olivine, plagioclase, and augite is restricted to temperatures below 1000 °C and pressures below 2500 bars, corresponding to <5.5 wt% water in the residual liquid. Although there is some evidence for mixing in the andesites (sporadic olivine phenocrysts), the broad theme of the history of both lava types is that the phenocryst assemblages for both the andesitic magmas and basaltic andesitic magmas are generated from degassing and reequilibration on ascent of initially hydrous parents containing greater than 6 wt% water. Indeed andesitic magmas could be related to a basaltic andesite parent by hornblende-plagioclase fractionation under the same hydrous conditions. Received: 10 December 1996 / Accepted: 21 August 1997  相似文献   

17.
Between 1759 and 1774, Jorullo Volcano and four associated cinder cones erupted an estimated 2 km3 of magma which evolved progressively with time from early, hypersthene-normative, primitive basalts to late-stage, quartz-normative, basaltic andesites. All lavas contain <6 vol% phenocrysts of magnesian olivine (Fo90-70) with Cr-Al-Mg-spinel inclusions, and microphenocrysts of plagioclase and augite; late-stage basaltic andesites also carry phenocrysts of plagioclase, augite, and rare orthopyroxene, hornblende pseudomorphs, and microphenocrysts of titanomagnetite. Olivine-melt compositions indicate liquidus temperatures ranging from 1,230° C to 1,070° C in the early- and late-stage lavas, respectively; \(f_{{\text{O}}_{\text{2}} } \) was about 0.6 log units above the Ni-NiO buffer in the early lavas but increased to 2.5 log units above Ni-NiO in the late lavas, perhaps through groundwater-magma interaction. Smooth major and trace element compositional trends in the lavas can be largely modeled by simple crystal fractionation of olivine, augite, plagioclase, and minor spinel. La, Ce, and other incompatible elements (Rb, Sr, Ba, Hf, Th, Ta), however, are anomalously enriched in the latestage lavas, whereas the heavy rare earth elements (Dy, Yb, Lu) are anomalously depleted. The modeled crystal fractionation event must have occurred at lower-crustal to upper-mantle pressures (8–15 kb), although the crystals actually present in the Jorullo lavas appear to have formed at low pressures. Thus, a two-stage crystallization history is implied. Despite the presence of granitic xenoliths in middle-stage lavas from Jorullo, bulk crustal assimilation appears to have played an insignificant role in generating the compositional trends among the lavas. As MgO decreases from 9.3 to 4.3 wt% through the suite, Al2O3 increases from 16.4 to 19.1 wt%. Most highalumina basalts reported in the literature have 18 to 21 wt% Al2O3, but are too depleted in MgO, Ni, and Cr to have been generated directly through mantle partial melting. These high-alumina basalts have probably undergone significant fractionation of olivine, augite, plagioclase, and spinel from primitive parental basalts similar to the early Jorullo lavas. Such primitive basalts are rarely erupted in mature arcs and may be completely absent from mature stratovolcanoes. Cerro La Pilita is a late-Quaternary cinder and lava cone centered just 3 km south of Jorullo. The primitive trachybasalts of Cerro La Pilita, however, are radically different from the Jorullo basalts. They are nepheline normative with high concentrations of K2O (>2.5 wt%), P2O5 (>0.9 wt%), Ba (1,200 ppm), Sr (>2,000 ppm), and many other incompatible elements, and contain crystals of hornblende and apatite in addition to olivine, spinel, augite, and plagioclase. The magmas of these two neighboring volcanoes cannot be related to one another by any simple mechanism, and must represent fundamentally different partial melting events in the mantle. The contrasts between Jorullo and Cerro La Pilita demonstrate the difficulty in defining simple relationships between magma type and distance from the trench in the Mexican Volcanic Belt.  相似文献   

18.
Major and trace element and isotopic ratios (Sr, Nd and Pb) are presented for mafic lavas (MgO > 4 wt%) from the southwestern Yabello region (southern Ethiopia) in the vicinity of the East African Rift System (EARS). New K/Ar dating results confirm three magmatic periods of activity in the region: (1) Miocene (12.3–10.5 Ma) alkali basalts and hawaiites, (2) Pliocene (4.7–3.6 Ma) tholeiitic basalts, and (3) Recent (1.9–0.3 Ma) basanite-dominant alkaline lavas. Trace element and isotopic characteristics of the Miocene and Quaternary lavas bear a close similarity to ocean island basalts that derived from HIMU-type sublithospheric source. The Pliocene basalts have higher Ba/Nb, La/Nb, Zr/Nb and 87Sr/86Sr (0.70395–0.70417) and less radiogenic Pb isotopic ratios (206Pb/204Pb = 18.12–18.27) relative to the Miocene and Quaternary lavas, indicative of significant contribution from enriched subcontinental lithospheric mantle in their sources. Intermittent upwelling of hot mantle plume in at least two cycles can explain the magmatic evolution in the southern Ethiopian region. Although plumes have been originated from a common and deeper superplume extending from the core–mantle boundary, the diversity of plume components during the Miocene and Quaternary reflects heterogeneity of secondary plumes at shallower levels connected to the African superplume, which have evolved to more homogeneous source.  相似文献   

19.
Aoba picrites in Vanuatu arc (Southwestern Pacific) offer the opportunity to address the question of the origin of Si-undersaturated arc magmas, through the geochemical study of their olivine-hosted melt inclusions. These latter delineate a differentiation trend of calc-alkaline silica-undersaturated basalts, with typical trace-element patterns of arc magmas. The most primitive melt inclusions, preserved in olivines with Fo ≥ 89, have normative nepheline compositions with CaO/Al2O3 > 0.8, but belong to three distinct populations differing in their enrichment or depletion in LILE, Cl, and alkalis (Rb, K). The dominant population is characterized by medium-LILE concentrations (La/Yb ~ 7–8) and represents the parental magma of the Aoba lavas. The two others (La/Yb ~ 20 and 2) are either significantly enriched or extremely depleted in LILE, Cl, and alkalis. This compositional variability of primitive magma batches requires the multi-stage mixing between melts generated by partial melting of both peridotite and clinopyroxene-rich lithologies. Medium-LILE magma derives from the mixing between peridotite- and clinopyroxenite-derived melts, whereas the high- and low-LILE melts involve amphibole-bearing and amphibole-free clinopyroxenite sources, respectively.  相似文献   

20.
An experimental investigation of plagioclase crystallization in broadly basaltic/andesitic melts of variable Ca# (Ca/(Ca+Na)*100) and Al# (Al/(Al+Si)*100) values and H2O contents has been carried out at high pressures (5 and 10 kbar) in a solid media piston-cylinder apparatus. The H2O contents of glasses coexisting with liquidus or near-liquidus plagioclases in each experiment were determined via an FTIR spectroscopic technique. This study has shown that melt Ca# and Al#, H2O content and crystallization pressure all control the composition of liquidus plagioclase. Increasing melt Ca# and Al# increase An content of plagioclase, whereas the effect of increasing pressure is the opposite. However, the importance of the role played by each of these factors during crystallization of natural magmas varies. Melt Ca# has the strongest control on plagioclase An content, but melt Al# also exerts a significant control. H2O content can notably increase the An content of plagioclase, up to 10 mol % for H2O-undersaturated melts, and 20 mol % for H2O-saturated melts. Exceptionally calcic plagioclases (up to An100) in some primitive subduction-related boninitic and related rocks cannot be attributed to the presence of the demonstrated amounts of H2O (up to 3 wt %). Rather, they must be due to the involvement of extremely refractory (CaO/Na2O>18) magmas in the petrogenesis of these rocks. Despite the refractory nature of some primitive MORB glasses, none are in equilibrium with the most calcic plagioclase (An94) found in MORB. These plagioclases were likely produced from more refractory melts with CaO/Na2O = 12–15, or from melts with exceptionally high Al2O3(>18%). Magmas of appropriate compositions to crystallize these most calcic plagioclases are sometimes found as melt inclusions in near liquidus phenocrysts from these rocks, but are not known among wholerock or glass compositions. The fact that such melts are not erupted as discrete magma batches indicates that they are effectively mixed and homogenized with volumetrically dominant, less refractory magmas. The high H2O contents (∼ 6 wt%) in some high-Al basaltic arc magmas may be responsible for the existence of plagioclases up to An95 in arc lavas. However, an alternative possibility is that petrogenesis involving melts with abnormally high CaO/Na2O values (> 8) may account for the presence of highly anorthitic plagioclases in these rocks. Received: 31 August 1993 / Accepted: 20 May 1994  相似文献   

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