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1.
Using our database of the compositions of melt inclusions and quenched glasses of basaltic magmas from mid-ocean ridges (MORB), the average concentrations and ratios of H2O, Cl, F, S, K2O, Ce, and Dy were determined in these magmas. Assuming that the concentration ratios of volatile components to K2O are constant in the MORB magmas and their sources (depleted mantle, DM), and taking an average K2O content in the DM of 72 ppm, the following average contents were estimated for the DM: 158 ppm H2O, 6.6 ppm Cl, and 8.3 ppm F. Using an S/Dy ratio of 212 for MORB melts and a Dy concentration of 0.531 ppm in the DM, the concentration of S in the DM was estimated as 113 ppm. Our value for the average content of Cl is much higher than estimates obtained by other authors. This discrepancy could be due either to the assimilation of crustal (and hydrospheric) Cl by MORB magmas or to the deep mantle recycling of Cl. The latter mechanism is supported by the statistically significant positive correlation of Cl with K2O, H2O, and F. Such a correlation is not consistent with the hypothesis of basaltic magma contamination by seawater-derived chloride brines. Similar to other surface processes, the assimilation of crustal material operates within the existing global correlations and disturbs them. Based on the average integrated degree of mantle melting and the average degree of MORB magma differentiation (0.05), the average contents of potassium and volatile components in N-MORB and E-MORB mantle sources were estimated as 39 and 126 ppm K2O, 103 and 197 ppm H2O, 4.0 and 10.7 ppm Cl, and 3.9 and 9.1 ppm F, respectively. It is not likely that normal MORB magmas can be derived from depleted mantle that experienced a previous partial melting event (for instance, during the extraction of the primordial continental crust in the Early Precambrian), which was referred to as the ultradepleted mantle. Ordinary (not ultradepleted) MORB magmas can be derived either by the melting of a zone enriched DM (for instance, progressively enriched in incompatible components with depth), which is hardly possible, or by the continuous addition (mixing) of an enriched component to the ultradepleted mantle at the expense of sediments and crustal materials involved in deep recycling.  相似文献   

2.
The effects of H2O, CO2, CH4 and HF on partial melting of a model phlogopite harzburgite mantle are considered with regard to the production of ultrapotassic magmas. Fluorine has a polymerising effect in H2O-poor conditions, but in the presence of abundant H2O where HF rather than F is dominant, the overall effect is depolymerisation. Methane also dissolves by forming (OH)– groups, and so has a depolymerising effect. Group I ultrapotassic rocks (lamproites) probably originate from primary magmas with SiO2 contents ranging from around 40 wt% to at least 52 wt%. This range can be explained by differing depths of origin from a similar source with a similar reduced H2O-CH4-HF volatile mixture. The formation of silica-rich initial melts from a model phlogopite harzburgite is assisted by the presence of CH4 and HF. Dissociation of less than 0.1 wt% H2O, driven by H2 loss, is sufficient to cause oxidation during emplacement to observed oxidation states. Silica-poor ultrapotassic rocks could be produced at higher pressures in a reduced environment, or in an oxidised environment with high CO2/(CO2 + H2O) ratios.Group II (African Rift) potassic rocks may originate in H2O-poor conditions in which fluorine will maintain a large phlogopite phase field, so that initial melts will be magnesian and silica-undersaturated.  相似文献   

3.
Volatiles and major elements in submarine glasses from Loihi seamount and Kilauea volcano. Hawaii were analyzed by high temperature mass spectrometry and the electron microprobe. Loihi glasses are subdivided into three groups: tholeiitic, transitional and alkali basalts. The glasses are evolved: Mg numbers range from 48–58. The alkalic lavas are the most evolved.Total volatiles range from 0.73 to 1.40 wt.%. H2O shows a positive linear correlation with K2O content [H2O = 0.83 (± .09) K2O + 0.08 (± .06)]. Concentrations of H2O are higher in the alkalic lavas, but Cl and F abundances are highly variable. Variations in ratios of incompatible elements (K2O, P2O5, H2O) indicate that each group was derived from a distinct source. CO2 contents range from 0.05 to 0.19 wt.% but show no systematic correlation with rock type or Mg #. A well-defined decrease in glass CO2 content with increasing vesicularity is shown by the alkalic lavas. CO2 may have been outgassed from the tholeiitic and transitional magmas prior to eruption during storage in a shallow magma chamber. Reduced carbon species (CO and CH4) were found in small amounts in most of the alkalic samples. Although the redox histories of Hawaiian lavas are poorly known, these new data indicate the presence of a reduced source for Loihi magmas.The Kilauea tholeiitic glasses are evolved (Mg # 48.3 to 55) and have higher H2O contents (av. 0.54 wt.%) than Loihi tholeiites (av. 0.42 wt.%) at the same Mg # (~55). Cl is distinctly lower in Kilauea glasses (0.01 wt.%) compared to Loihi glasses (0.09 wt.%). The data indicate significant source differences for the two volcanoes, consistent with results of other geochemical studies.Loihi tholeiites have distinctly higher 3He/4He ratios than Kilauea tholeiites and are the highest measured in submarine basalts (KURZ et al., 1983). These high ratios have been used to invoke a primitive source for Loihi basalts. The high Cl content of these basalts, the highest we have ever measured in submarine basalts, may be a fingerprint of this primitive source, as previously noted for Icelandic basalts (Schillinget al. 1980).  相似文献   

4.
Textural evidence for the partial breakdown of staurolite-biotite and andalusite-biotite assemblages to cordierite-orthoamphibole implies high temperature metasomatic depletion of K2O in semi-pelitic rocks from Springton, South Australia. The origin of the reaction textures is discussed with reference to K2O-T diagrams derived from the topologically equivalent K2O–(-H2O) diagram showing both discontinuous and Fe–Mg continuous reactions. The involvement of fluids in the metasomatic process is implied by the scale of K2O removal and suggests that the outcrop pattern of cordierite-gedrite rocks reflects, at least in part, a heterogeneous distribution of advecting fluids in the metamorphic pile at high temperatures.Mineral abbreviations used in text and figures ab albite - alm almandine - als aluminosilicate - and andalusite - anth anthophyllite - bt biotite - cd cordierite - fe-bt Fe-rich biotite - fe-cd Fe-rich cordierite - fe-oa Fe-rich orthoamphibole - fe-st Fe-staurolite - gt garnet - ksp potassium feldspar - ky kyanite - mg-cd Mg-rich cordierite - mg-oa Mg-rich orthoamphibole - mg-st Mg-rich staurolite - mu muscovite - oa orthoamphibole - phl phlogopite - plag plagioclase - py pyrope - sill sillimanite - st staurolite - v vapour  相似文献   

5.
The Serra Geral (Paraná) continental flood basalt (SG-CFB) province in Brazil is associated with the Jurassic-Cretaceous breakup of Gondwanaland and the transition of continental to oceanic magmatism during the opening of the South Atlantic Ocean. A suite of 24 samples representative of the SG-CFB in Rio Grande do Sul, southern Brazil, shows a compositional continuum from basalt (50–53 wt% SiO2, Mg# 60-45), to basaltic andesite, to andesite, rhyodacite, and rhyolite (73 wt% SiO2). Certain compositional aspects of the mafic rocks (e.g., TiO2, K2O, CaO, Zr/Nb, Zr/Y, Ti/Zr) resemble those of basaltic dikes and flows associated with the opening of the North Atlantic Ocean.Fractionation trends are apparent in MgO variation diagrams and calculations show that basalt-basaltic andesite continuums are largely due to removal of plagioclase and clinopyroxene. These mafic rocks can be categorized as (i) having higher or lower incompatible-element contents (e.g. K2O 0.6–1.5 wt%; Rb 12–43 ppm; Ba 125–240 ppm) due to incorporation of Brazilian Archean crust or rhyolitic magma by basalt from a particular source material or to partial-melting differences of that source, and (ii) as having higher or lower TiO2, Sr, Ba, and P contents due to source heterogeneities. Crustal components are obvious in certain basaltic samples, as where K2O > 1 wt%, SiO2 > 51%, and TiO2 1%, but are insignificant in others (e.g., compositions close to those of South Atlantic basin basalts). Calculations indicate origins for intermediate and silicic rocks by removal of pl, cpx, and Ti-magnetite from basaltic andesite, but crust and magma-mixing affecting basaltic-andesite fractionates were likely also involved. Where contamination is insignificant, Zr, Nb, and Y abundances indicate T-type MORE source material like that for certain S. Atlantic Ocean basalts. Source material was essentially a 91 hybrid of N-type and P-type MORB components. N-type MORB lithosphere followed SG-CFB because decompression due to rifting crust enabled partial melting of uppermost (depleted) mantle.  相似文献   

6.
Rabaul caldera is a large volcanic depression at the north-east tip of New Britain, Papua New Guinea. The lavas range in composition from basalt to rhyolite and have a calc-alkalic affinity but also display features typical of tholeiites, including moderate absolute iron enrichment in flows cropping out around the caldera. The basalts contain phenocrysts of plagioclase and clinopyroxene with less abundant olivine and titanomagnetite. In the basaltic andesites olivine is rare, while orthopyroxene and titanomagnetite are common along with plagioclase and clinopyroxene. Orthopyroxene is also found mantling olivine in some of the basalts while in both rock types pigeonitic augite is a fairly common constituent of the groundmass. Plagioclase in both basalt and basaltic andesite often exhibits sieve texture and analysis of the glass blebs show them to be of similar composition to the bulk rock. Phenocrystic clinopyroxene is a diopsidic augite in both basalt and basaltic andesite. Al2O3 content of the clinopyroxene is moderately high (4%) and often shows considerable variation in any one grain. Calculations show that the microphenocrysts probably crystallised near the surface, while phenocrysts crystallised at around 7 kb (21 km). Neither the basalts nor the basaltic andesites would have been in equilibrium at any geologically reasonable P and T with quartz eclogite. Equilibration between mantle peridotite and a. typical Rabaul basaltic liquid could have occurred around 35 kb and 1270 °C. A basaltic andesite liquid yields a temperature of 1263 °C and a pressure of 28 kb for equilibration with mantle peridotite.Partial melting of sufficient volumes of mantle peridotite at these P's and T's requires about 15% H2O, but there is no evidence that these magmas ever contained large amounts of water. It is proposed that the Rabaul magmas were initially generated by partial melting of subducted lithosphere and subsequently modified by minor partial melting as they passed through the overlying mantle peridotite.  相似文献   

7.
Glass inclusions in olivine and diopside phenocrysts from pyroclasts of various eruptions of Vesuvius are representative of the magmas that supplied the volcano in the last 4–5000 years. During this interval the volcano alternated between open conduit activity (e.g. 1944 and 1906 eruptions) with long pauses interupted by Plinian and sub-Plinian eruptions (e.g. 3360 B.P. Avellino, A.D. 79 Pompei, A.D. 472 Pollena). The eruptive behaviour was conditioned in all cases by the presence of shallow reservoirs: two cases are distinguished: (1) small and very shallow, 1906-type; (2) large and deeper Plinian-sub-Plinian magma chamber. Lapilli of 1906 lava fountains contain olivine (Fo89.5–90.4) including Cr-spinel [Cr/(Cr+Al)] (Cr#>75) and volatile-K-rich tephritic glasses, which represent the first recognized Vesuvius primary magmas. Mg-poorer olivine (Fo83–89) also occurs in 1906 and 1944 products; it formed within the shallow reservoir, together with pyroxene and leucite, between 1200 and 1130°C, from K-tephritic melts (MgO=6–8 wt%). The Plinian and sub-Plinian pumices contain diopside, phlogopite and minor olivine (Fo85–87) representing adcumulates wrenched from the chamber walls. Glass inclusions in diopside (and some olivine) range from K-basalt to K-tephrite (MgO=6–8 wt%), with homogenization temperature of 1130–1170°C. They have been regarded as representative of the magmas supplying the Plinian-sub-Plinian chamber(s). The Avellino glass inclusions have K-basaltic compositions, contrasting with the mostly K-tephritic Pompei and Pollena inclusions. They display lower C1 and P contents with respect to the younger tephritic melts, and these variations should reflect primary features of the mantle-derived magmas. The primary and the near-primary Vesuvius magmas, as illustrated by melt inclusions, emphasize high K, P and volatile (H2O, Cl, F, S) contents, with high K2O/H2O (2–2.5), Cl/F (2.5) and Cl/S (2–3) ratios, consistent with a metasomatized mantle source, and distinguishing the Vesuvius potassic primary magmas from those of the northern part of the Roman Province.  相似文献   

8.
High temperature mass spectrometric analyses of glasses from quenched pillow rims of andesites dredged from 1170 m water depth in the northern portion of the Mariana Island arc indicate substantially less H2O (~ 1 wt.%) and more CO2 (~ 0.24 wt.%) than previously reported for volcanic arc rocks. Glass-vapor inclusions within plagioclase phenocrysts from quenched rims have CO2H2O ratios of 1:1. These results are similar to analyses of basaltic samples from the Mariana Trough (a back-arc basin). Generally, F and Cl contents are higher and S lower in the arc rocks compared to the samples from the back-arc basin. These results favor models for the production of island arc magmas which involve melting of the subducted slab, rather than just melting of the overlying mantle wedge because of the high volatile content needed to produce island arc magmas from peridotite (10–15 wt.%). The trough samples, although similar in non-volatile composition to mid-ocean ridge rocks, have much higher H2O. somewhat higher CO2 and lower S contents. Either near surface addition of voiatiles has enriched the magmas or H2O must be a more important component in the generation and evolution of back-arc basin lavas than in the genesis of mid-ocean ridge basalts.  相似文献   

9.
Crystallization experiments of basaltic andesite mafic endmember from the 24 ka Lower Pollara eruption (Salina, Aeolian Islands, Italy) were investigated at 200 MPa, 950–1100 °C, in the H2O activity (aH2O) range ~0.3 to 1, and at two ranges of oxygen fugacity (fO2) between ~FMQ to FMQ+1 and ~FMQ+2 to FMQ+3.3 (log bars, FMQ is fayalite-magnetite-quartz). Comparison of the produced phase assemblages and phase compositions with the natural sample reveals that the storage conditions were ~1050 °C, ~2.8 wt% H2O in the melt (aH2O ~0.5), and relatively oxidizing (~FMQ+2.5). The composition of plagioclase in the groundmass indicates a period of cooling to ≤950 °C. The overall differentiation trends of the Salina volcanics can be explained by fractional crystallization close to H2O saturated conditions (~5 wt% H2O in the melt at 200 MPa) and most likely by accumulation of plagioclase, i.e., in basaltic andesites, and by various degree of mixing–mingling between the corresponding differentiates. The slightly elevated K2O contents of the most mafic basaltic andesites that can be found in the lowermost unit of the Lower Pollara pyroclastics reveal earlier processes of moderately hydrous fractional crystallization at higher temperature (>~1050 °C). Fractional crystallization with decreasing influence of H2O causes a moderate decrease of MgO and a significant increase of K2O relative to SiO2 in the residual liquids. It is exemplarily shown that the crystallization of SiO2-rich phases at high temperature and low aH2O of only moderately K2O-rich calc-alkaline basalts can produce shoshonitic and high potassic rocks similar to those of Stromboli and Volcano. This suggests that the observed transition from calc-alkaline to shoshonitic and high potassic volcanism at the Aeolian Arc over time can be initiated by a general increase of magmatic temperatures and a decrease of aH2O in response to the extensional tectonics and related increase of heat flow and declining influence of slab-derived fluids.  相似文献   

10.
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11.
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   

12.
Granitoid rocks of the compositionally zoned Late Cretaceous Toulumne Intrusive Suite in the central Sierra Nevada, California, have initial87Sr/86Sr values (Sri) and143Nd/144Nd values (Ndi) that vary from 0.7057 to 0.7067 and from 0.51239 to 0.51211 respectively. The observed variation of both Sri and Ndi and of chemical composition in rocks of the suite cannot be due to crystal fractionation of magma solely under closed system conditons. The largest variation in chemistry, Ndi, and Sri is present in the outer-most equigranular units of the Tuolumne Intrusive Suite. Sri varies positively with SiO2, Na2O, K2O, and Rb concentrations, and negatively with Ndi, Al2O3, Fe2O3, MgO, FeO, CaO, MnO, P2O5, TiO2, and Sr concentrations. This covariation of Sri, Ndi and chemistry can be modeled by a process of simple mixing of basaltic and granitic magmas having weight percent SiO2 of 48.0 and 73.3 respectively. Isotopic characteristic of the mafic magma are Sri=0.7047, Ndi=0.51269 and 18O=6.0, and of the felsic magma are Sri=0.7068, Ndi=0.51212 and 18O=8.9. The rocks sampled contain from 50 to 80% of the felsic component. An aplite in the outer equigranular unit of the Tuolumne Intrusive Suite apparently was derived by fractional crystallization of plagioclase and hornblende from magma with granudiorite composition that was a product of mixing of the magmas described above. Siliceous magmas derived from the lower crust, having a maximum of 15 percent mantle-derived mafic component, are represented by the inner prophyritic units of the Tuolumne Intrusive Suite.  相似文献   

13.
Calc-alkaline granitoid rocks of the Oligocene-Pliocene Chilliwack batholith, North Cascades, range from quartz diorites to granites (57–78% SiO2), and are coeval with small gabbroic stocks. Modeling of major element, trace element, and isotopic data for granitoid and mafic rocks suggests that: (1) the granitoids were derived from amphibolitic lower crust having REE (rare-earth-element) and Sr-Nd isotopic characteristics of the exposed gabbros; (2) lithologic diversity among the granitoids is primarily the result of variable water fugacity during melting. The main effect of fH 2 O variation is to change the relative proportions of plagioclase and amphibole in the residuum. The REE data for intermediate granitoids (quartz diorite-granodiorite; Eu/Eu*=0.84–0.50) are modeled by melting with fH 2 O<1 kbar, leaving a plagioclase + pyroxene residuum. In contrast, data for leucocratic granitoids (leuco-granodiorites and granites; Eu/Eu* =1.0–0.54) require residual amphibole in the source and are modeled by melting with fH 2 O=2–3 kbar. Consistent with this model, isotopic data for the granitoids show no systematic variation with rock type (87Sr/86Sri =0.7033–0.7043; Nd(0)=+3.3 to +5.5) and overlap significantly with data for the gabbroic rocks (87Sr/86Sri =0.7034–0.7040; Nd(0)=+3.3 to +6.9). The fH 2 O variations during melting may reflect additions of H2O to the lower crust from crystallizing basaltic magmas having a range of H2O contents; Chillwack gabbros document the existence of such basalts. One-dimensional conductive heat transfer calculations indicate that underplating of basaltic magmas can provide the heat required for large-scale melting of amphibolitic lower crust, provided that ambient wallrock temperatures exceed 800°C. Based on lithologic and geochemical similarities, this model may be applicable to other Cordilleran batholiths.  相似文献   

14.
The average compositions (including H2O, Cl, F, and S contents) and chemical structure of oceanic mantle plumes were estimated on the basis of the ratios of incompatible volatile components, potassium, and some other elements in the basaltic magmas of ocean islands (melt inclusions and quenched glasses). The following average concentrations were estimated for the plume mantle: 510 ppm K2O, 520 ppm H2O, 21 ppm Cl, 55 ppm F, and 83 ppm S; these values are significantly higher than those of the depleted mantle (except for S). The abundances of H2O, Cl, and S are lower than in the primitive mantle. The normalized H2O content in the plume mantle is similar to the concentrations of similarly incompatible La and Ce but lower than the concentrations of K2O, Cl, and Sr. This is at odds with the idea of wet mantle plumes. Three types of basaltic magmas corresponding to three types of plume sources (M1, M2, and M3) were distinguished. The concentrations of incompatible elements in these reservoirs were estimated using two models, assuming either an isochemical mantle or a moderately enriched composition of plume material. The latter model gave the following average concentrations of H2O, Cl, F, and S: 130, 33, 11, and 110 ppm for M1, 110, 12, 65, and 45 ppm for M2; 530, 29, 49, and 110 ppm for M3. The plume mantle is not homogeneous, and its heterogeneity is related to the existence of three main compositions, one of which (M1) is similar to the mantle of mid-ocean ridges, and two others (M2 and M3) are moderately enriched in K2O, TiO2, P2O5, F, and incompatible trace elements. The compositions of M2 and M3 are strongly different in H2O, Cl, and S contents. The M2 mantle reservoir is significantly poorer in these components and richer in incompatible trace elements than M3. The plume mantle was formed mainly by the mixing of three sources: ultradepleted mantle, moderately enriched relatively dry mantle, and moderately enriched H2O-rich mantle. In addition to the three main components of the plume mantle, there are probably minor components enriched in chlorine and depleted in fluorine. It is supposed that all these components are entrained into the plume mantle through the mantle recycling of components of the oceanic and continental crust. The established relationships are in agreement with the zonal model of a mantle plume, which includes a hot central part poor in H2O, Cl, and S; an outer part enriched in volatile and nonvolatile incompatible elements; and enclosing mantle material interacting with the plume.  相似文献   

15.
Changes in magmatic assemblages and crystal stability as a response of CO2-flushing in basaltic systems have rarely been directly addressed experimentally, making the role of CO2 in magma dynamics still controversial and object of scientific debate. We conducted a series of experiments to understand the response of magmas from Etna volcano to CO2 flushing. We performed a first experiment at 300 MPa to synthesize a starting material composed of crystals of some hundreds of µm and melt pools. This material is representative of an initial magmatic assemblage composed of plagioclase, clinopyroxene and a water-undersaturated melt with 1.6 wt% H2O. In a second step, the initial assemblage was equilibrated at 300 and 100 MPa with fluids having different XCO 2 fl (CO2/(H2O + CO2)). At low XCO 2 fl (< 0.2 to 0.4), plagioclase is completely dissolved and clinopyroxene show dissolution textures. For relatively high XCO 2 fl (0.9 at 300 MPa), the flushing of a CO2-rich fluid phase leads to an increase of the amount of clinopyroxene and a decrease of the abundance of plagioclase at 300 MPa. This decrease of plagioclase proportion is associated with a change in An content. Our experiments demonstrate that flushing basaltic systems with fluids may drastically affect crystal textures and phase equilibria depending on proportions of H2O and CO2 in the fluid phase. Since texture and crystal proportions are among the most important parameters governing the rheology of magmas, fluid flushing will also influence magma ascent to the Earth’s surface. The experimental results open new perspectives to decipher the textural and compositional record of minerals observed in volcanic rocks from Mt. Etna, and at the same time offer the basis for interpreting the information preserved in minerals from other basaltic volcanoes erupting magmas enriched in CO2.  相似文献   

16.
Amphibole has been discussed to potentially represent an important phase during early chemical evolution of arc magmas, but is not commonly observed in eruptive arc rocks. Here, we present an in-depth study of metastable calcic amphibole megacrysts in basaltic andesites of Merapi volcano, Indonesia. Radiogenic Sr and Nd isotope compositions of the amphibole megacrysts overlap with the host rock range, indicating that they represent antecrysts to the host magmas rather than xenocrysts. Amphibole-based barometry suggests that the megacrysts crystallised at pressures of >500 MPa, i.e., in the mid- to lower crust beneath Merapi. Rare-earth element concentrations, in turn, require the absence of magmatic garnet in the Merapi feeding system and, therefore, place an uppermost limit for the pressure of amphibole crystallisation at ca. 800 MPa. The host magmas of the megacrysts seem to have fractionated significant amounts of amphibole and/or clinopyroxene, because of their low Dy/Yb ratios relative to the estimated compositions of the parent magmas to the megacrysts. The megacrysts’ parent magmas at depth may thus have evolved by amphibole fractionation, in line with apparently coupled variations of trace element ratios in the megacrysts, such as e.g., decreasing Zr/Hf with Dy/Yb. Moreover, the Th/U ratios of the amphibole megacrysts decrease with increasing Dy/Yb and are lower than Th/U ratios in the basaltic andesite host rocks. Uranium in the megacrysts’ parent magmas, therefore, may have occurred predominantly in the tetravalent state, suggesting that magmatic fO2 in the Merapi plumbing system increased from below the FMQ buffer in the mid-to-lower crust to 0.6–2.2 log units above it in the near surface environment. In addition, some of the amphibole megacrysts experienced dehydrogenation (H2 loss) and/or dehydration (H2O loss), as recorded by their variable H2O contents and D/H and Fe3+/Fe2+ ratios, and the release of these volatile species into the shallow plumbing system may facilitate Merapi’s often erratic eruptive behaviour.  相似文献   

17.
Water Content of Basalt Erupted on the ocean floor   总被引：1，自引：0，他引：1  
Deep sea pillow basalts dredged from the ocean floor show that vesicularity changes with composition as well as with depth. Alkalic basalts are more vesicular than tholeiitic basalts erupted at the same depth. The vesicularity data, when related to experimentally determined solubility of water in basalt, indicate that K-poor oceanic tholeiites originally contained about 0.25 percent water, Hawaiian tholeiites of intermediate K-content, about 0.5 percent water, and alkali-rich basalts, about 0.9 percent water. Analyses of fresh basalt pillows show a systematic increase of H2O+ as the rocks become more alkalic. K-poor oceanic tholeiites contain 0.06–0.42 percent H2O+, Hawaiian tholeiites, 0.31–0.60 percent H2O+, and alkali rich basalts 0.49–0.98 percent H2O+. The contents of K2O, P2O5, F, and Cl increase directly with an increase in H2O+ content such that at 1.0 weight percent H2O+, K2O is 1.58 percent, P2O5 is 0.55 percent, F is 0.07 percent, and Cl is 0.1 percent. The measured weight percent of deuterium on the rim of one Hawaiian pillow is –6.0 (relative to SMOW); this value, which is similar to other indications of magmatic water, suggests that no appreciable sea water was absorbed by the pillow during or subsequent to eruption on the ocean floor.Concentrations of volatile constituents in the alkali basalt melts relative to tholeiitic melts can be explained by varying degrees of partial melting of mantle material or by fractional crystallization of a magma batch.Publication authorized by the Director, U.S. Geological Survey.  相似文献   

18.
Based on the generalization of data on melt inclusions and quenched glasses, the average compositions of subduction (island arc and active continental margin settings) basic magmas were estimated. The main geochemical features of the average composition of these magmas are significant depletion in Nb and Ta, less significant depletion in Ti, Zr, and Sm, and enrichment in Cl, H2O, F, and P in the primitive mantlenormalized patterns. The average normalized contents of moderately incompatible HREE in these magmas are close to those in the basic magmas of other geodynamic settings. Subduction basic magmas exhibit negative correlation of Li, Y, Dy, Er, Yb, Lu, and Ti contents with MgO content. Most of incompatible elements (Nb, Ta, U, Th, LREE) do not correlate with MgO, but correlate with each other and K2O. Variations in element contents are related to crystallization differentiation, magma mixing, and possibly, participation of several sources. The water content in the island arc basic magmas varies from almost zero value to more than 6 wt %. Most compositions are characterized by weak negative correlation between H2O and MgO contents, but some compositions define a negative correlation close to that in magmas of mid-ocean ridges (MOR). Considered magmas demonstrate distinct positive correlation between MgO content and homogenization temperature, practically coinciding with that of MOR magmas. Modeling of phase equilibria revealed widening of crystallization field of olivine in the magmas of subduction zones compared to MOR magmas. This can be related to the high water content in subduction magmas. Simultaneous liquidus crystallization of olivine and clinopyroxene in subduction magmas occurs at pressure approximately 5 kbar higher than that of MOR magmas. Based on the average ratios of trace element to K2O content, we determined the average compositions for subduction magma sources. Relative to depleted mantle, they are enriched in all incompatible elements, with positive anomalies of U, Rb, Ba, B, Pb, Cl, H2O, F, and S, and negative anomalies of Th, K, Be, Nb, Ta, Li, Nd, Pb, and Ti. A general elevated content of incompatible elements indicates a reworking of the rocks of mantle wedge by fluids and melts that were released from the upper layers of subducted plate.  相似文献   

19.
Summary ¶The Campanian Ignimbrite rock samples include two compositionally distinct populations of clinopyroxene phenocrysts, and the entrapped MI (melt inclusions) are also different in composition. The cores of the more MgO-enriched phenocrysts carry basaltic trachyandesite MI that contain >6wt.% MgO, whereas other phenocrysts contain MI with <4wt.% MgO. The MgO-enriched MI also contain comparatively greater abundances of F, CaO, TiO2, P2O5, SO2, and Sr and show marginally higher ratios of (CaO/Al2O3) than the low-MgO MI. Most of the high-MgO MI also contain comparatively more H2O. The MgO-enriched MI are restricted to diopsidic clinopyroxenes and show minimal compositional variability, demonstrating that they were derived from a common magmatic source or sources. We interpret these MI to represent primary, mafic magma. In contrast, the more evolved, low-MgO melt inclusions, which are restricted to salitic clinopyroxenes, span the compositional range of trachyandesite to trachyte. The low-MgO fractions of Campanian Ignimbrite magma evolved via fractional crystallization with or without mingling or mixing with more primitive, high-MgO magma.Interestingly, the MI from the Giugliano sample also cluster into low-MgO and high-MgO fractions, and the evolutionary trends for major, minor, and trace elements mirror those exhibited by the Campanian Ignimbrite MI, suggesting that both magmas were derived from similar or the same source(s) and that the processes of magma evolution were equivalent for both magmas.The MI also indicate that the Campanian Ignimbrite and Giugliano magmas did not form by evolution of Taurano magma, because the geochemical trends expressing melt evolution of the former and latter magmas are too dissimilar. Most Taurano MI show higher (CaO/Al2O3) and contain less SiO2, (Na2O+K2O), Cl, Li, Rb, Cs, Sr, Nb, Th, and U than the high-MgO and low-MgO Campanian Ignimbrite and Giugliano MI, indicating that the Taurano MI represent magmas which were much more primitive.Received July 15, 2002; revised version accepted March 27, 2003  相似文献   

20.
A spatially abrupt geochemical boundary is preserved within four plutonic complexes along the western margin of the Cretaceous Idaho Batholith near McCall, Idaho. These intrusives ranging in composition from tonalite to granite were emplaced across a regional boundary between accreted oceanic-arc terranes and the continental margin, and their isotopic, major-element, and trace-element geochemistry provide detailed information about this change in crustal characteristics at depth, indicating that the boundary is nearly vertical and extends deep into the lithosphere. The Hazard Creek complex, emplaced west of the transition in wall-rock lithology, has initial 87Sr/86Sr (Ri) less than 0.7045 and 18O greater than 7.5, indicating little or no continental crust in its source region; however, elevated 18O requires some incorporation of rocks formed or altered at the earth's surface. A large shift in Ri and 18O is observed across the 5–8 km wide Little Goose Creek complex, which was emplaced across the wall-rock boundary. This is interpreted as mixing between: (1) a basaltic or andesitic magma with low K2O and high Na2O, Al2O3, and Sr, similar to that forming the Hazard Creek complex; and (2) materials similar to Precambrian sedimentary sedimentary rocks with low Sr, high 18O (+15) and high Ri (0.83 at 100 Ma). The Payette River complex, emplaced east of the wall-rock boundary, exhibits at least one additional component with low 18O (+6), moderate Ri (0.708) and mafic composition. This component is inferred to be old basaltic material in the lower crust or upper mantle similar to that inferred to be a minor part of the Peninsular Ranges Batholith in SE California (Silver et al. 1979; Hill et al. 1986). The easternmost complex in the Idaho transect is made up of granites that may contain a component of granitic cratonal basement. The entire west-to-east geochemical transition from oceanic-arc magmas to cratonal magmas takes place over a lateral distance of less than 20 km. Although the zone of transitional protolith dominated by metasedimentary rocks is unusually narrow and may have been in part tectonically removed, the striking geochemical similarities between this traverse and several other transects across much broader areas of Nevada and California suggest that the craton itself was not rifted apart, but that juxtaposition of the accreted oceanic-arc terranes occurred along the preexisting craton margin. The data confirm that the isotopic geochemistry of granitoid plutons can be used as a probe of deep lithospheric character, and that major lateral variations in the lithosphere on the order of one to two kilometers in width can be recognized in favorable circumstances.  相似文献   

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