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1.
Mount Hasan is a double-peaked stratovolcano, located in Central Anatolia, Turkey. The magmas erupted from this multi-caldera complex range from basalt to rhyolite, but are dominated by andesite and dacite. Two terminal cones (Big Mt. Hasan and Small Mt. Hasan) culminate at 3253 m and 3069 m respectively. There are four evolutionary stages in the history of the volcanic complex (stage 1: Kecikalesi volcano, 13 Ma, stage 2: Palaeovolcano, 7 Ma, stage 3: Mesovolcano and stage 4: Neovolcano). The eruptive products consist of lava flows, lava domes, and pyroclastic rocks. The later include ignimbrites, phreatomagmatic intrusive breccias and nuées ardentes, sometimes reworked as lahars. The total volume is estimated to be 354 km3, the area extent 760 km2. Textural and mineralogical data suggest that both magma mixing and fractional crystallization were involved in the generation of the andesites and dacites. The magmas erupted from the central volcanoes show a transition with time from tholeite to calc-alkaline. Three generations of basaltic strombolian cones and lava flows were emplaced contemporaneously with the central volcanoes. The corresponding lavas are alkaline with a sodic tendency.  相似文献   

2.
Rejuvenated-stage tuff cones (Honolulu Volcanics) on Koolau volcano, Oahu, Hawaii, contain xenoliths of Koolau shield basalt. Because Koolau subaerial shield lavas represent a Hawaiian geochemical 'end member', and submarine shield lavas have compositions with some affinities to Mauna Loa and Kilauea, we analyzed 28 xenolithic basalts from Salt Lake and Koko Head cones to determine how these seemingly random samplings of the Koolau profile compare to established Koolau geochemistry. Analyses reveal that 24 are shield tholeiitic basalt—the focus of this study—and 4 are rejuvenated-stage basaltic rocks. The tholeiitic xenoliths represent largely upper Koolau shield lavas, as these samples (8.3 to 5.8 wt% MgO) have, with one exception, overall major- and trace-element compositions that overlap those of Koolau subaerial shield lavas. Secondary processes, however, created some distinctions—namely, enrichments/depletions in K, Ba, Sr, SiO2, and FeO, and, due to zeolitization (chabazite with attending okenite and apophyllite), elevated CaO. One xenolithic basalt with 8.2 wt% MgO has higher Ti, Zr, Nb, and Sc, and lower Zr/Nb than subaerial lavas, and appears to represent relatively early, deeper shield—thereby reinforcing that the Koolau shield source varied temporally. Olivine, orthopyroxene, and plagioclase are the phenocrysts (clinopyroxene is rare), and their core compositions range widely across the suite—Fo87.8–72, orthopyroxene Mg#s 85–72, and An74–60. Several xenolithic basalts have both normally and reversely zoned orthopyroxene and plagioclase with a variety of core compositions (e.g., orthopyroxene-core Mg#s 82, 77, and 72, all in one sample). These compositions and zonations record evidence for wide compositional ranges of replenishment (MgO ~13–8 wt%) and reservoir (MgO ~7 to <5 wt%) magmas mixing in varying proportions; however, extreme MgO lavas (~13 and <5 wt%) are not observed as either subaerial or xenolithic basalt, but are indicated by phenocryst cores of Fo87.8 and orthopyroxene-Mg# 72. The Koolau magma-mixing history resembles that of Kilauea, and is unlike the 'steady-state' mixing known for Mauna Loa. Finally, these basalt samples show that any xenolithic occurrence of Koolau lava is subject to the zeolitization prevalent in the tuff-cone hosts.Editorial handling: M. Carroll  相似文献   

3.
Small euhedral chromite crystals are found in olivine macrophenocrysts (Fo80–84) from the basaltic andesites (150 ppm Cr) erupted in 1943–1947, and in orthopyroxene macrophenocrysts of the andesites (75 ppm Cr) erupted in 1947–1952. The majority of the chromite octahedra are 5–20 μm in diameter, and some are found in clusters and linear chains of three or more oriented chromite crystals. The composition of the majority of the chromite grains within olivine and orthopyroxene macrophenocrysts is Fe2+/(Fe2++Mg)=0.5–0.6, Cr/(Cr+Al)=0.5–0.6 and Fe3+/(Fe3++Al+Cr)=0.2–0.3. The chromite crystals in contact with the groundmass are larger, subhedral, and grade in composition from chromite cores to magnetite rims. Comparison of the composition of chromite with those of other volcanic rocks shows that the most primitive Paricutin chromite is richer in total iron and higher in Fe3+/(Fe3++Al+Cr) than primary chromite in most lavas. The linear chains of oriented chromite octahedra are found in olivine and orthopyroxene macrophenocrysts, and in the groundmass. These chromite chains are thought to result from diffusion-controlled crystallization because of the very high partition coefficient (1000) of Cr between chromite and melt. We conclude that chromite was a primary phase in the lavas at the time of extrusion and that magnetite only crystallized after extrusion during cooling of the lava flows. The presence of chromite microphenocrysts in andesitic lavas containing as little as 70 ppm Cr can be explained by dissolved H2O in the melt depressing the liquidus temperature for orthopyroxene such that chromite becomes a liquidus phase. The influence of dissolved H2O can also explain the lack of plagioclase macrophenocrysts in most of the lavas and the relatively high partition coefficient (20) of Ni between olivine and melt and the high partition coefficient (40) of Cr between orthopyroxene and melt. The liquidus temperature of the basaltic andesite is estimated to have been less than 1140°C, assuming H2O>1 wt.%, and the log fO2 to have been above that of the QFM buffer. The chromite and orthopyroxene liquidus temperature of the andesites, assuming H2O>1 wt.%, is estimated to have been 1100°C or less. The derivation of the later andesites from the earlier basaltic andesites has been explained by a combination of fractional crystallization of olivine, orthopyroxene and plagioclase, and assimilation of xenoliths. The significantly lower Cr, Ni and Mg of the andesites may have been in part due to the separation of olivine macrophenocrysts plus enclosed chromite crystals from the earlier basaltic andesites.  相似文献   

4.
Arenal volcano in Costa Rica has been erupting nearly continuously, but at a diminishing rate, since 1968, producing approximately 0.35 km3 of lavas and tephras that have shown consistent variations in chemistry and mineralogy. From the beginning of the eruption in July 1968 to early 1970 (stage 1, vol.=0.12 km3) tephras and lavas became richer in Ca, Mg, Ni, Cr, Fe, Ti, V, and Sc and poorer in Al2O3 and SiO2. Concentrations of incompatible trace elements (including Sr) decreased by 5%–20%. Phenocryst contents increased 20–50 vol%. During stage 2 (1970–1973, vol. = 0.13 km3) concentrations of compatible trace elements rose, and concentrations of incompatible trace elements either remained constant or also rose. Al2O3 contents decreased by 1 wt%. Phenocryst content increased slightly, principally due to increased orthopyroxene. During stage 3 (mid-1974 to the present, vol.= 0.10 km3) concentrations of SiO2 increased by 1 wt%, compatible trace elements decreased slightly, and incompatible trace element concentrations increased by 5% to 10%. Although crystals increased in size during stage 3, their overall abundance stayed roughly constant.Our modeling suggests that early stage-1 magmas were produced by boundary layer fractionation under high-p H2O conditions of an unseen basaltic andesitic magma that intruded into the Arenal system after approximately 500 B.P. Changes in composition during stage 2 resulted from mixing of this more mafic original magma with new magma that had a similar SiO2 content, but higher compatible and incompatible element concentrations. The changes during stage 3 resulted from continued influx of the same magma plus crystal removal.We conclude that the eruption proceeded in the following way. Before 1968 zoned stage-1 magma resided in the deep crust below Arenal. A new magma intruded into this chamber in July 1968 causing ejection of the stage-1 magmas. The intruding magma mixed with mafic portions of the original chamber producing the mixed lavas of stage 2. Continued mixing plus crystal fractionation along the chamber and conduit walls produced stage-3 lavas. The time scales of crustal level magmatic processes at Arenal range 100–103 years, which are 3–6 orders of magnitude shorter than those of larger, more silicic systems.  相似文献   

5.
This paper addresses formation of felsic magmas in an intra‐oceanic magmatic arc. New bathymetric, petrologic, geochemical, and isotopic data for Zealandia Bank and two related volcanoes in the south‐central Mariana arc is presented and interpreted. These three volcanoes are remnants of an older andesitic volcano that evolved for some time and became dormant long enough for a carbonate platform to grow on its summit before reawakening as a rhyodacitic volcano. Zealandia lavas are transitional between low‐ and medium‐K and tholeiitic and calc‐alkaline suites. They define a bimodal suite with a gap of 56–58 wt% SiO2; this suggests that mafic and felsic magmas have different origins. The magmatic system is powered by mantle‐derived basalts having low Zr/Y and flat rare earth element patterns. Two‐pyroxene thermometry yields equilibration temperatures of 1000–1100 °C for andesites and 900–1000 °C for dacites. Porphyritic basalts and andesites show textures expected for fractionating magmas but mostly fine‐grained felsic lavas do not. All lavas show trace element signatures expected for mantle and crustal sources that were strongly melt‐depleted and enriched by subduction‐related fluids and sediment melts. Sr and Nd isotopic compositions fall in the normal range of Mariana arc lavas. Felsic lavas show petrographic evidence of mixing with mafic magma. Zealandia Bank felsic magmatism supports the idea that a large mid‐ to lower‐crustal felsic magma body exists beneath the south‐central Mariana arc, indicating that MASH (mixing, assimilation, storage, and homogenization) zones can form beneath intra‐oceanic as well as continental arcs.  相似文献   

6.
The Torfajökull central volcano in south-central Iceland contains the largest volume of exposed silicic extrusives in Iceland (225 km3). Within SW-Torfajökull, postglacial mildly alkalic to peralkalic silicic lavas and lava domes (67–74 wt.% SiO2) have erupted from a family of fissures 1–2.5 km apart within or just outside a large caldera (12×18 km). The silicic lavas show a fissure-dependent variation in composition, and form five chemically distinct units. The lavas are of low crystallinity (0–7 vol.%) and contain phenocrysts in the following order of decreasing abundance: plagioclase (An10-40), Na-rich anorthoclase (<Or23), clinopyroxene (Fs37-20), FeTi oxides (Usp32-60; Ilm93-88), hornblende (edenitic–ferroedenitic) and olivine (Fo22-37), with apatite, pyrrhotite and zircon as accessory phases. The phenocryst assemblage (0.2–4.0 mm) consistently exhibits pervasive disequilibrium with the host melt (glass). Xenoliths include sparse, disaggregated, and partially fused leucocratic fragments as well as amphibole-bearing rocks of broadly intermediate composition. The values of the silicic lavas are in the range 3.6–4.4, and these are lower than the values of comagmatic, contemporaneous basaltic extrusives within SW-Torfajökull, implying that the former can not be derived from the latter by simple fractional crystallization. FeTi-oxide geothermometry reveals temperatures as low as 750–800°C. To explain the fissure-dependent chemical variations, depletions, low FeTi-oxide temperatures and pervasive crystal-melt disequilibrium, we propose the extraction and collection of small parcels of silicic melt from originally heterogeneous basaltic crustal rock through heterogeneous melting and wall rock collapse (solidification front instability, SFI). The original compositional heterogeneity of the source rock is due to (1) silicic segregations, in the form of pods and lenses characteristically formed in the upper parts of gabbroic intrusives, and (2) extreme isostatic subsidence of the earlier, less differentiated lavas of the Torfajökull central volcano. Ridge migration into older crustal terranes, coupled with establishment of concentrated volcanism at central volcanoes like Torfajökull due to propagating regional fissure swarms, supplies the heat source for this overall process. Continued magmatism in these fissures promotes extensive prograde heating of older crust and the progressive vitality and rise of the central volcano magmatic system that leads to, respectively, SFI and subsidence melting. The ensuing silicic melts (with relict crystals) are extracted, collected and extruded before reaching complete internal equilibrium. Chemically, this appears as a two-stage process of crystal fractionation. In general, the accumulation of high-temperature basaltic magmas at shallow depths beneath the Icelandic rift zones and major central volcanoes, coupled with unique tectonic conditions, allows large-scale reprocessing and recycling of the low- , hydrothermally altered Icelandic crust. The end result is a compositionally bimodal proto-continental crust.  相似文献   

7.
The extensive, complex, continental flood basalt (CFB) province which occurs in Ethiopia and Yemen consists of Oligocene prerift volcanism related to the Africa–Arabia continental break-up. Basalts from the northwestern Ethiopian Plateau exhibit a particularly large range of compositions and, for the first time in the Afro-Arabian CFB province, low-Ti basalts have been encountered. Major and some trace element data have been used to identify distinct geochemical groups and evaluate the role of differentiation processes. Three magma types have been distinguished: two high-Ti groups (HT1 and HT2) and one low-Ti group (LT). The transitional to tholeiitic LT suite exhibits low TiO2 (1–2.6%), Fe2O3* (10.5–14.8%), CaO/Al2O3 (0.4–0.75), Nb/La (0.55–0.85) and high SiO2 (47–51%). In contrast, the HT2 suite exhibits high TiO2 (2.6–5%), Fe2O3* (13.1–14.7%), CaO/Al2O3 (0.9–1.43), Nb/La (1.1–1.4) and low SiO2 (44–48.3%). The HT1 series is intermediate between the LT and HT2 groups. These three groups of lavas originated from different parental magmas. They display distinct differentiation trends, either controlled by the removal of a shallow level gabbroic (Pl+Ol+Cpx) assemblage (LT and HT1 suites) or by deeper Ol+Cpx fractionation (HT2 suite). Most of this thick continental flood lava pile was emplaced over a short time interval (about 1–2 Ma). The three contrasted magma types do not reflect a temporal evolution of their sources but rather a strong spatial control. Indeed, the northwestern Plateau may be subdivided into two different subprovinces as all the low-Ti basalts are located in the northern part of the plateau, and the high-Ti basalts are exposed in the eastern and southern parts. The LT and HT1 basalts display compositional ranges similar to those of the low- and high-Ti groups from other main CFB provinces (e.g. Parana, Deccan, Karoo, Siberia, …). However, the HT2 group exhibits extreme OIB-like compositions. This unusual geochemical signature suggests the involvement of deep mantle in the genesis of the HT2 magmas. The LT compositions rather reflect the participation of the continental lithosphere, through mantle derived melts and/or crustal contamination.  相似文献   

8.
Calc-alkaline rocks of the Hasan Dagi volcano (Central Anatolia, Turkey) are products of arc volcanism triggered by continental collision. Volcanic rocks of the Hasan Dagi range in composition from basalt to rhyolite but are dominated by andesite and dacite. Considering only the mass transfer part of the process leads to an incomplete picture of magma chamber processes. The exclusion of simultaneous calculations of heat and mass transfer between mixing magmas, however, has prevented petrologists from gaining new insights into the magma mixing process. Thus, we report our experimental results in conjunction with modeling with MELTS to test the ideas concerning the petrogenesis of Hasan Dagi volcanic rocks and quantitatively model the relevant petrogenetic processes. Our results demonstrate that the chemical diversity of Hasan Dagi volcano is inconsistent with the closed-system crystallization and differentiation. Thus, (1) our experimental modeling, (2) the agreement between the liquid line of descent defined by the natural rock data and the MELTS calculations, and (3) the agreement between the mineralogy of the rocks and calculated mineralogy corroborate the conclusion that the isobaric–isenthalpic magma mixing of basalt and rhyolite is the major controlling process in the petrogenesis of the Hasan Dagi magmas.  相似文献   

9.
Basalt and diabase from the Cretaceous Dumisseau Formation, southern Haiti have Mg-numbers of 43–63, TiO2 contents of 1.6–3.9% and La abundances of 3.6–15.3 ppm.La/Ta ratios average 10, and indicate that the basalts are oceanic in character, distinct from the arc associations forming the northern part of Haiti. Oldest lavas have low TiO2 (1.6%) and are LREE-depleted, similar to N-MORBs, whereas overlying lavas have higher TiO2 (2–3.9%) and are LREE-enriched, similar to E-MORBs or hotspot basalts.87Sr86Sr ratios vary from 0.70280 to 0.70316,143Nd144Nd from 0.512929 to 0.513121, and206Pb204Pb from 19.00 to 19.27. LREE-depleted lavas have high143Nd144Nd (0.51309–0.51310) typical of MORBs, whereas143Nd144Nd in the LREE-enriched lavas varies widely (0.512929–0.513121).Chemical features of the Dumisseau basalts are equivalent to those of Caribbean seafloor basalts recovered on DSDP Leg 15, and support the contention that the Dumisseau is an uplifted section of Caribbean Sea crust. Oldest lavas are analogous to MORB-like basalts cored at Leg 15 Sites 146, 150, 152 and 153, and the overlying lavas are analogous to incompatible-element-enriched basalts cored at Site 151 on the Beata Ridge. Isotopic compositions of the Dumisseau basalts overlap with those of the eastern Pacific Galapagos and Easter Island hotspots. However, the presence of N-MORB basalts in the lower part of the Dumisseau and at the majority of Leg 15 Sites indicates that the anomalously thick Caribbean crust probably did not originate as a hotspot-related basaltic plateau, but may have been generated by on-ridge or near-ridge hotspot magmatism.  相似文献   

10.
Fluorine contents in about 160 representative Quaternary volcanic rocks and 15 hornblende and biotite phenocrysts in a calc-alkali series in Japan have been determined by a selective ion-electrode method. Tholeiites have the lowest contents and the narrowest range (58–145 ppm), while alkali basalts have the highest contentws and the widest range (301–666 ppm), high-alumina basalts have intermediate values (188–292 ppm). F contents in basalts clearly increase from east to west across the Japanese Islands, as do alkalies, P2O5 REE, U, Th and H2O.The volcanic rocks studied are divided into two groups on the basis of F: (1) witt, increasing % SiO2 or advancing fractionation, F contents show either progressive enrichment; or (2) with increasing fractionation, F contents show rather constant values. The former is produced by fractionation of anhydrous phases from basalt to mafic andesite magmas; the tholeiite series of Nasu volcanic zone (outer zone), northeastern, Japan is a typical example. The latter group is derived through separation of amphibole-bearing phases from basaltic magmas at various depths from upper mantle (about 30 km) to upper crust; the alkali series in southwestern Japan and the calc-alkali series of Chokai volcanic zone (inner zone), northeastern Japan, are examples.  相似文献   

11.
Island arc and continental margin (i.e. western Americas) lavas are divided (based on raw data from literature) into basalts (defined by absence of Ca-poor pyroxene, dominated by quartz-normative tholeiites); basaltic andesites and andesites (subdivided on basis of breaks in SiO2 histogram and taken as <56% and 56–63% SiO2; Ca-poor pyroxene present; amphibole and biotite absent); and hornblende (±biotite) lavas, which prove to be mainly relatively silicic andesites. Relative proportions of these types are (576 samples): 23% basalts, 29% basaltic andesites; 30% andesites; 18% hornblende andesites. The compilation emphasizes the dominance of calcic plagioclase (labradorite-anorthite) amongst the phenocryst phases. Pyroxenes are largely augite and hypersthene (En60–75); olivine (Fo65–85) is common through all compositions. There is an overall close similarity in chemistry and mineralogy between continental margin and island arc lavas, although small consistent differences are apparent (e.g. K2O, TiO2, P2O5).Modal data indicate that 70% of lavas are phenocryst-rich (20–60 vol.%), and that phenocryst contents show a bimodal distribution. Statistically and petrologically significant correlations are found between mineralogy and rock chemistry, most notably between total rock Al2O3 and modal phenocrystic plagioclase (found in all data groups, except hornblende andesites). This, and related data and correlations, indicate that the majority of orogenic magmas are modified by crystal fractionation (including crystal accumulation) processes dominated by plagioclase, and interpreted to occur under relatively low pressures. Dominance of plagioclase suggests phenocryst precipitation occurs typically in water-undersaturated magmas.  相似文献   

12.
The extinct Pleistocene volcano Muriah, situated behind the main Pleistocene—Recent Sunda magmatic arc in north-central Java, has erupted at least two contrasted groups of lavas. One group forms a well-defined compositional series (Anhydrous Series) from leucite basanite to tephritic phonolite, with olivine and tschermakitic clinopyroxene the main phenocrysts. The other group, the “Hydrous Series”, includes compositionally variable tephrites and high-K andesites with common plagioclase, biotite and amphibole. Lavas of the Anhydrous Series are much richer in LIL trace elements than the most potassic lavas of neighbouring active volcanoes, but relative HFS element enrichment is less pronounced. REE patterns have almost constant slopes from La (250–600 times chondrites) to Yb (5–10 times chondrites), while those of lavas of active centres are less light-enriched, and show flattening in the heavy REE. Anhydrous Series initial 87Sr/86Sr ratios (0.7043–0.7046) are lower than those of active centres (0.7047–0.7053). Hydrous Series lavas are intermediate in all these geochemical characteristics.The most mafic A-series leucite basanite, with Mg/(Mg + Fe2+) 0.69, 140 ppm Ni and 620 ppm Cr was probably derived from the primary magma for the series by fractionation of only 5 wt.% olivine. Its REE pattern suggests derivation from a garnet-bearing source. Experiments on this basanite, with up to 10% olivine and 20% orthopyroxene added, and in the presence of H2O and H2O/CO2 mixtures, have shown that for all but very high magma water contents, the olivine and garnet liquidus fields are widely separated by fields of phlogopite and clinopyroxene. There is no liquidus field of orthopyroxene. Hence, if magma production involved an equilibrium melting process alone, the most probable sources are of garnet-bearing phlogopite clinopyroxenite type. Alternatively, this magma may represent the end-product of interaction between a low-K basanite magma from a garnet lherzolite source in the asthenosphere and a phlogopite-bearing lherzolite zone in the lower lithosphere. Its production was probably related to crustal doming and extension superimposed on the dominant subduction regime. Hydrous Series magmas may have resulted from mixing between Anhydrous Series magmas and high-K calc-alkaline basaltic to andesitic magmas more directly related to subduction processes.  相似文献   

13.
A geochemical and isotopic study of lavas from Pichincha, Antisana and Sumaco volcanoes in the Northern Volcanic Zone (NVZ) in Ecuador shows their magma genesis to be strongly influenced by slab melts. Pichincha lavas (in fore arc position) display all the characteristics of adakites (or slab melts) and were found in association with magnesian andesites. In the main arc, adakite-like lavas from Antisana volcano could be produced by the destabilization of pargasite in a garnet-rich mantle. In the back arc, high-niobium basalts found at Sumaco volcano could be produced in a phlogopite-rich mantle. The strikingly homogeneous isotopic signatures of all the lavas suggest that continental crust assimilation is limited and confirm that magmas from the three volcanic centers are closely related. The following magma genesis model is proposed in the NVZ in Ecuador: in fore arc position beneath Pichincha volcano, oceanic crust is able to melt and produces adakites. En route to the surface, part of these magmas metasomatize the mantle wedge inducing the crystallization of pargasite, phlogopite and garnet. In counterpart, they are enriched in magnesium and are placed at the surface as magnesian andesites. Dragged down by convection, the modified mantle undergoes a first partial melting event by the destabilization of pargasite and produces the adakite-like lavas from Antisana volcano. Lastly, dragged down deeper beneath the Sumaco volcano, the mantle melts a second time by the destabilization of phlogopite and produces high-niobium basalts. The obvious variation in spatial distribution (and geochemical characteristics) of the volcanism in the NVZ between Colombia and Ecuador clearly indicates that the subduction of the Carnegie Ridge beneath the Ecuadorian margin strongly influences the subduction-related volcanism. It is proposed that the flattening of the subducted slab induced by the recent subduction (<5 Ma?) of the Carnegie Ridge has permitted the progressive warming of the oceanic crust and its partial melting since ca. 1.5 Ma. Since then, the production of adakites in fore arc position has deeply transformed the magma genesis in the overall arc changing from ‘typical’ calc-alkaline magmatism induced by hydrous fluid metasomatism, to the space- and time-associated lithology adakite/high-Mg andesite/adakite-like andesite/high-Nb basalts characteristic of slab melt metasomatism.  相似文献   

14.
Subduction-related volcanism in the Nevados de Payachata region of the Central Andes at 18°S comprises two temporally and geochemically distinct phases. An older period of magmatism is represented by glaciated stratocones and ignimbrite sheets of late Miocene age. The Pleistocene to Recent phase (0.3 Ma) includes the twin stratovolcanoes Volcan Pomerape and Volcan Parinacota (the Nevados de Payachata volcanic group) and two small centers to the west (i. e., Caquena and Vilacollo). Both stratovolcanoes consist of an older dome-and-flow series capped by an andesitic cone. The younger cone, i. e., V. Parinacota, suffered a postglacial cone collapse producing a widespread debris-avalanche deposit. Subsequently, the cone reformed during a brief, second volcanic episode. A number of small, relatively mafic, satellitic cinder cones and associated flows were produced during the most recent activity at V. Parinacota. At the older cone, i. e., V. Pomerape, an early dome sequence with an overlying isolated mafic spatter cone and the cone-forming andesitic-dacitic phase (mostly flows) have been recognized. The two Nevados de Payachata stratovolcanoes display continuous major- and trace-element trends from high-K2O basaltic andesites through rhyolites (53%–76% SiO2) that are well defined and distinct from those of the older volcanic centers. Petrography, chemical composition, and eruptive styles at V. Parinacota differ between pre- and post-debris-avalanche lavas. Precollapse flows have abundant amphibole (at SiO2 > 59 wt%) and lower Mg numbers than postcollapse lavas, which are generally less silicic and more restricted in composition. Compositional variations indicate that the magmas of the Nevados de Payachata volcanic group evolved through a combination of fractional crystallization, crustal assimilation, and intratrend magma mixing. Isotope compositions exhibit only minor variations. Pb-isotope ratios are relatively low (206Pb/204Pb = 17.95–18.20 and208Pb/204Pb = 38.2–38.5);87Sr/86Sr ratios range 0.70612–0.70707,143Nd/144Nd ratios range 0.51238–0.51230, and 18OSMOW values range from + 6.8%o to + 7.6%o SMOW. A comparison with other Central Volcanic Zone centers shows that the Nevados de Payachata magmas are unusually rich in Ba (up to 1800 ppm) and Sr (up to 1700 ppm) and thus represent an unusual chemical signature in the Andean arc. These chemical and isotope variations suggest a complex petrogenetic evolution involving at least three distinct components. Primary mantle-derived melts, which are similar to those generated by subduction processes throughout the Andean arc, are modified by deep crustal interactions to produce magmas that are parental to those erupted at the surface. These magmas subsequently evolve at shallower levels through assimilation-crystallization processes involving upper crust and intratrend magma mixing which in both cases were restricted to end members of low isotopic contrast.  相似文献   

15.
The Palei-Aike volcanic field, the southernmost unit of the Patagonian plateau lavas, consists of Pleistocene to Recent alkali olivine basalts petrologically and geochemically similar to alkali basalts from diverse tectonic environments. The Palei-Aike basalts have lower SiO2 and Al2O3 and higher TiO2 and P2O3 than published analyses of other Patagonian plateau basalts. Garnet, garnet + spinel-, and phlogopite-peridotites, not reported from other Patagonian plateau lavas or from elsewhere in South America, are common inclusions within Palei-Aike lavas along with spinel-lherzolite, dunite, granulites, and aluminous clinopyroxene megacrysts. The inclusion of these high-pressure assemblages indicates a mantle origin for the Palei-Aike lavas. The Patagonian plateau lavas are located in a tectonic position similar to back-arc basins, and their origin may be a consequence of subduction. The origin and distinct chemical features of the Palei-Aike basalts may be due in part to thermal or mechanical perturbations of the mantle related to changes in plate boundaries and motions in the vicinity of the unstable trench-transform triple junction formed by the South American, Antarctic and Scotia plates.  相似文献   

16.
The Plio-Quaternary volcanic rocks of the south-central Andes (southward from latitude 18°S) contain two associations: calc-alkaline and shoshonitic which coincide with seismic belts as geographically distinct zones aligned parallel to the oceanic trench. There is a continuous gradation from calc-alkaline to shoshonitic associations. The shoshonitic association appears to the north of latitude 26°S; southwards, the calc-alkaline association directly abuts against the continental (Argentinian) alkaline association.Thirty-one lavas from the Plio-Quaternary calc-alkaline Socompa, Lascar, Sairecabur and Tocorpuri and shoshonitic Sierra de Lipez volcanoes were studied. The lavas are porphyric with abundant glass. The distribution and the nature of the phenocrysts vary according to the chemistry of the calc-alkaline lavas. Petrographic evidence for crystal fractionation has been observed. Occasional phenocrysts of alkali feldspars occur in the shoshonitic lavas. The K2O and SiO2 contents increase from calc-alkaline to shoshonitic lavas with distance away from the oceanic trench. In lavas from Socompa, Lascar, Sairecabur and Tocorpuri calc-alkaline volcanoes, K2O, Li and Rb increase and K/Rb and Sr decrease with increasing SiO2; Ba increases with decreasing Sr, probably as a result of plagioclase fractionation. In lavas from Sierra de Lípez shoshonitic volcano, SiO2 is high, K2O is high and rather constant and Li, Rb, Ba and Sr increase with increasing SiO2. Bolivian shoshonitic lavas appear to be genetically related to the calc-alkaline suite.The calc-alkaline lavas may be derived by crystal fractionation from a parental magma of andesitic nature that originated in or above the subjacent Benioff zone.  相似文献   

17.
Submersible investigations along the East Rift segments, the Pito Deep and the Terevaka transform fault of the Easter microplate eastern boundary, and on a thrust-fault area of the Nazca Plate collected a variety of basalts and dolerites. The volcanics consist essentially of depleted (N-MORB), transitional (T-MORB) and enriched (E-MORB) basalts with low (0.01−0.1, < 0.7), intermediate (0.12–0.25, 0.7–1.2) and high (> 0.25, > 1.2–2) K/Ti and(La/Sm)N ratios, respectively. The Fe-Ti-rich ferrobasalt encountered among the N-MORBs are found on the Pito Deep Central volcano, on the Terevaka intra-transform ridge, on the ancient (< 2.5 Ma) Easter microplate (called EMP, comprising the East Rift Inner pseudofaults and Pito Deep west walls) and on thrust-fault crusts. The most enriched (T- and E-MORB) volcanics occur along the East Rift at 25 °50′–27 °S (called 26 °S East Rift) and on the Pito seamount located near the tip of the East Rift at 23 °00′–23 °40′S (called 23 °S East Rift). The diversity in incompatible element ratios of the basalts in relation to their structural setting suggests that the volcanics are derived from a similar heterogenous mantle which underwent variable degrees of partial melting and magma mixing. In addition the Pito seamount volcanics have undergone less crystal fractionation (< 20%) than the lavas from the other Easter microplate structures (up to 35–45%). The tectonic segmentation of the East Rift observed between 23 and 27 °S corresponds to petrological discontinuities related to Mg# variations and mantle melting conditions. The highest Mg# (> 61) are found on topographic highs (2000–2300 m) and lower values (Mg# < 56) at the extremities of the East Rift segments (2500–5600 m depths). The deepest area (5600 m) along the East Rift is located at 23 °S and coincides with a Central volcano constructed on the floor of the Pito Deep. Three major compositional variabilities of the volcanics are observed along the East Rift segments studied: (1) the 26 °S East Rift segment where the volcanics have intermediate Na8 (2.5–2.8%) and Fe8 (8.5–11%) contents; (2) the 23 °S East Rift segment (comprising Pito seamount and Pito Deep Central volcano) which shows the highest (2.9–3.4%) values of Na8 and a low (8–9%) Fe8 content; and (3) the 25 °S (at 24 °50′–26 °10′S) and the 24 °S (at 24 °10′–25 °S) East Rift segments where most of the volcanics have low to intermediate Na8 (2.6–2.0%) and a high range of Fe8 (9–13%) contents. When modeling mantle melting conditions, we observed a relative increase in the extent of partial melting and decreasing melting pressure. These localized trends are in agreement with a 3-D type diapiric upwelling in the sense postulated by Niu and Batiza (1993). Diapiric mantle upwelling and melting localized underneath the 26, 25 and 23 °S (Pito seamount and Central volcano) East Rift segments are responsable for the differences observed in the volcanics. The extent of partial melting varies from 14 to 19% in the lithosphere between 18 and 40 km deep as inferred from the calculated initial (Po=16kbar) and final melting (Pf=7kbar) pressures along the various East Rift segments. The lowest range of partial melting (14–16%) is confined to the volcanics from 23 °S East Rift segment including the Pito seamount and the Central volcano. The Thrust-fault area, and the Terevaka intra-transform show comparable mantle melting regimes to the 25 and 26 °S East Rift segments. The older lithosphere of the EMP interior is believed to have been the site of high partial melting (17–20%) confined to the deeper melting area (29–50 km). This increase in melting with increasing pressure is similar to the conditions encountered underneath the South East Pacific Rise (13–20 °S).  相似文献   

18.
We present the initial results of a quantitative investigation of the volatile geochemistry of Deception Island, an active volcano situated near the spreading axis of a Quaternary ensialic marginal basin (Bransfield Strait, northern Antarctic Peninsula). Fluorine contents in Deception Island magmas (112–461 ppm) are comparable with lavas from a range of tectonic environments but F-K2O relationships most closely compare with continental flood basalts and lavas from island arcs and some marginal basins. Boron contents are high (4.3–16.3 ppm) and the values overlap with those of arc lavas; they provide strong support for the presence of a mantle source component derived from the slab subducted at the coeval trench (by melting at the slab/wedge interface and/or during slab dehydration). Both F and B acted incompatibly in Deception Island magmas but there is significant variation in incompatible-element ratios such as K/F, K/B, P/F, P/B, which strongly suggests that the magmatic system was open to some or all of these elements during differentation. The variations in these ratios also provide evidence for the presence of at least two stages in the magmatic evolution of the volcano. During pre-caldera times, mafic magma was emplaced into the upper crust where it evolved and may have reacted with the crustal envelope, thus changing the contents of some or all of the elements F, B, K and P and their inter-element ratios. A later, large influx of hot, mafic magma into the chamber may have been responsible for a major eruption that ultimately led to the formation of the caldera. K/F, K/B, etc, ratios in the magma chamber were “reset” and subsequently continued to change, possibly by further crustal interaction during melt evolution in post-caldera times.  相似文献   

19.
A bimodal volcanic suite with KAr ages of 0.05–1.40 Ma was collected from the Sumisu Rift using alvin. These rocks are contemporaneous with island arc tholeiite lavas of the Izu-Ogasawara arc 20 km to the east, and provide a present day example of volcanism associated with arc rifting and back-arc basin initiation. Major element geochemistry of the basalts is most similar to that of basalts found in other, more mature back-arc basins, which indicates that back-arc basins need not begin their magmatic evolution with lavas bearing strong arc signatures.Volatile concentrations distinguish Sumisu Rift basalts from island arc basalts and MORB. H2O contents, which are at least four times greater than in MORB, suppress plagioclase crystallization. This suppression results in a more mafic fractionating assemblage, which prevents Al2O3 depletion and delays the initiation of Fe2O3(tot) and TiO2 enrichment. However, unlike arc basalts,Fe3+/ΣFe ratios are only slightly higher than in MORB and are insufficient to cause magnetite saturation early enough to suppress Fe2O3(tot) and TiO2 enrichment. Thus, major element trends are more similar to those of MORB than arcs.H2O, CO2 and S are undersaturated relative to pure phase solubility curves, indicating exsolution of an H2O-rich mixed gas phase. HighH2O/S, highδD, and low (MORB-like)δ34S ratios are considered primary and distinctive of the back-arc basin setting.  相似文献   

20.
The Nevado Sabancaya in southern Peru has exhibited a persistent eruptive activity over eight years following a violent eruption in May–June 1990. The explosive activity consisted of alternated vulcanian and phreatomagmatic events, followed by declining phreatic activity since late 1997. The mean production rate of magma has remained low (106–107 m3 per year).The 1990–1998 eruptive episode produced andesitic and dacitic magmas. The juvenile tephra span a narrow range of compositions (60–64 wt% SiO2). While SiO2 contents do vary slightly, they do not show any systematic variation with time. Phenocryst assemblages in the juvenile rocks consist of mainly plagioclase, associated with high-Ca pyroxene, hornblende, biotite, and iron-titanium oxides. Rare fine-grained magmatic enclaves, with angular to subrounded shapes, are contained within some of the juvenile lava blocks, which were expelled since 1992. They have a homogeneous andesitic composition (57 wt% SiO2) and show randomly oriented interlocking columnar or acicular crystals (plagioclase and amphibole), with interstitial glass and a few voids, which define a quench-textured groundmass.Textural, mineralogical and chemical evidence suggests that the 1990–1998 eruptions have mainly erupted hybrid andesites, except for the 1990 dacite. The hybrid andesites contain a mixed population of plagioclase phenocrysts: Ca-rich clear plagioclase (An40–60), Na-rich clear plagioclase (An25–35), and inversely zoned dusty-rimmed plagioclase with a sodic core (An25–40) surrounded by a Ca-rich mantle (An45–65). Melt-inclusions, wavy dissolution surfaces and stepped zoning within the dusty-rimmed plagioclases are compatible with resorption induced by magma recharge events. Chemical and isotopic lines of evidence also show that andesites are hybrids resulting from magma mixing processes. Repeated magma recharge, incomplete homogenisation and different degrees of crustal assimilation may explain the extended range of isotopic signatures.Our study leads to propose an evolution model for the magmatic system at Nevado Sabancaya. The main magma body consisted of dacitic magmas differentiating through extensive open-system crystallization (AFC). Repeated recharge of more mafic magmas induced magma mixing, leading to the formation of hybrid andesites. A partially crystalline boundary layer formed at the interface between the andesites and the recharge magma. The magmatic enclaves were produced by the disruption and dispersion of this andesitic layer as a result of new magma injection and/or sustained tectonic activity.Periodic magma recharge and interactions with groundwater are two processes that have enabled the explosive regime to remain persistent over an 8-year-long period. What precise mechanism triggers the eruptive activity remains speculative, but it may be related either to new magma injection, or to the sustained tectonic activity that occurred at that time in the vicinity of the volcano, or a combination of both.  相似文献   

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