Evolving metasomatic agent in the Northern Andean subduction zone, deduced from magma composition of the long-lived Pichincha volcanic complex (Ecuador)

Geochemical studies of long-lived volcanic complexes are crucial for the understanding of the nature and composition of the subduction component of arc magmatism. The Pichincha Volcanic Complex (Northern Andean Volcanic Zone) consists of: (1) an old, highly eroded edifice, the Rucu Pichincha, whose lavas are mostly andesites, erupted from 1,100 to 150 ka; and (2) a younger, essentially dacitic, Guagua Pichincha composite edifice, with three main construction phases (Basal Guagua Pichincha, Toaza, and Cristal) which developed over the last 60 ka. This structural evolution was accompanied by a progressive increase of most incompatible trace element abundances and ratios, as well as by a sharp decrease of fluid-mobile to fluid-immobile element ratios. Geochemical data indicate that fractional crystallization of an amphibole-rich cumulate may account for the evolution from the Guagua Pichincha andesites to dacites. However, in order to explain the transition between the Rucu Pichincha andesites and Guagua Pichincha dacites, the mineralogical and geochemical data indicate the predominance of magma mixing processes between a mafic, trace-element depleted, mantle-derived end-member, and a siliceous, trace-element enriched, adakitic end-member. The systematic variation of trace element abundances and ratios in primitive samples leads us to propose that the Rucu Pichincha magmas came from a hydrous-fluid metasomatized mantle wedge, whereas Guagua Pichincha magmas are related to partial melting of a siliceous-melt metasomatized mantle. This temporal evolution implies a change from dehydration to partial melting of the slab, which may be associated with an increase in the geothermal gradient along the slab due to the presence of the subducted Carnegie Ridge at the subduction system. This work emphasizes the importance of studying arc-magma systems over long periods of time (of at least 1 million of years), in order to evaluate the potential variations of the slab contribution into the mantle source of the arc magmatism.     

Adakitic magmas in the Ecuadorian Volcanic Front: Petrogenesis of the Iliniza Volcanic Complex (Ecuador)

The Iliniza Volcanic Complex (IVC) is a poorly known volcanic complex located 60 km SSW of Quito in the Western Cordillera of Ecuador. It comprises twin peaks, North Iliniza and South Iliniza, and two satellite domes, Pilongo and Tishigcuchi. The study of the IVC was undertaken in order to better constrain the role of adakitic magmas in the Ecuadorian arc evolution. The presence of volcanic rocks with an adakitic imprint or even pristine adakites in the Ecuadorian volcanic arc is known since the late 1990s. Adakitic magmas are produced by the partial melting of a basaltic source leaving a garnet rich residue. This process can be related to the melting of an overthickened crust or a subducting oceanic crust. For the last case a special geodynamic context is required, like the subduction of a young lithosphere or when the subduction angle is not very steep; both cases are possible in Ecuador. The products of the IVC, made up of medium-K basaltic andesites, andesites and dacites, have been divided in different geochemical series whose origin requires various interactions between the different magma sources involved in this subduction zone. North Iliniza is a classic calc-alkaline series that we interpret as resulting from the partial melting of the mantle wedge. For South Iliniza, a simple evolution with fractional crystallization of amphibole, plagioclase, clinopyroxene, magnetite, apatite and zircon from a parental magma, being itself the product of the mixing of 36% adakitic and 64% calc-alkaline magma, has been quantified. For the Santa Rosa rhyolites, a slab melting origin with little mantle interactions during the ascent of magmas has been established. The Pilongo series magma is the product of a moderate to high degree (26%) of partial melting of the subducting oceanic crust, which reached the surface without interaction with the mantle wedge. The Tishigcuchi series shows two stages of evolution: (1) metasomatism of the mantle wedge peridotite by slab melts, and (2) partial melting (10%) of this metasomatized source. Therefore, the relative ages of the edifices show a geochemical evolution from calc-alkaline to adakitic magmas, as is observed for several volcanoes of the Ecuadorian arc.     

安徽女山橄榄岩包体的氧同位素比值和微量元素组成：地幔交代作用

本文的研究对象是9个来自安徽女山新生代玄武岩的橄榄岩包体,利用激光氟化技术系统分析了橄榄石、单斜辉石和斜方辉石的氧同位素比值;利用LA-ICPMS技术分析了单斜辉石的微量元素组成。结果显示,女山橄榄岩存在辉石与橄榄石之间的氧同位素不平衡分馏现象,其中△Cpx-Ol18O(=δ18OCpx-δ18OOl)出现低至-0．5‰的负值;含角闪石包体中的单斜辉石明显富集大离子亲石元素(LILE,如Sr、Th、LREE)和亏损高场强元素(HFSE,如Nb、Zr、Ti)。氧同位素的数据表明,女山上地幔曾经经历过俯冲洋壳流体参与的交代作用,根据单斜辉石和橄榄石之间氧同位素分馏值△Cpx-Ol18O与包体形成深度之间的负相关性,提出了一个“上升 缓冲”的流体交代模型。虽然微量元素特征也表明女山上地幔受到过地壳流体的影响,但是氧同位素的不平衡分馏和LILE的富集／HFSE的亏损并不是同步的,对这种现象的可能解释是:引起氧同位素不平衡分馏的交代作用和造成女山单斜辉石微量元素特征的交代作用不是同一期的,即女山上地幔曾经发生过至少2次交代事件。     

Rainfall chemistry: long range transport versus below cloud scavenging. A two-year study at an inland station (Opme, France)

The present study investigates the chemical composition of wet atmospheric precipitation samples on a daily and an intra-event timescales in Opme, an experimental meteorological station located near Clermont-Ferrand, France. The samples have been collected from November 2005 to October 2007. A total of 217 rainwater samples, integrated for 24 h, were collected and analyzed for pH, conductivity, Na⁺, K⁺, Mg²⁺, NH₄⁺, Ca²⁺, Cl⁻, NO₃⁻ , SO₄²⁻ , PO₄³⁻ and HCO₃⁻. The composition of the rainwater collected appeared to be controlled by the following potential sources: neutralisation process (association among calcium, ammonium with nitrate and sulphate), marine and terrestrial sources. In order to determine the role of long-range transport, the integrated events were classified according to four origins of air-masses: (1) West, (2) North and East, (3) South including Iberian and Italian Peninsulae and (4) local. This analysis allows identifying the source areas of the different association of elements defined. Although calcium is always dominant, total content of rainfall is variable and neutralisation process can be more or less efficient and specific. Rainout (long-range transport) and washout (below-cloud scavenging) were investigated through intra-event measurements of chemical species. Four rain-events have been selected according to the four classes of origins of air-masses. It appears that the first fractions are responsible for an important part of the chemical content of the whole event. Terrestrial species, locally emitted, induce the neutralisation process of acid species. Local meteorological conditions, such as wind’s speed and direction, play an important role as they could provoke recharges of the below cloud air column during the event.     

Trace element distribution in peridotite xenoliths from Tok, SE Siberian craton: A record of pervasive, multi-stage metasomatism in shallow refractory mantle

Spinel peridotite xenoliths in alkali basalts at Tok, SE Siberian craton range from fertile lherzolites to harzburgites and wehrlites; olivine-rich (70-84%) rocks are dominant. REE patterns in the lherzolites range from nearly flat for fertile rocks (14-17% cpx) to LREE-enriched; the enrichments are positively correlated with modal olivine, consistent with high-permeability of olivine-rich rocks during melt percolation. Clinopyroxene in olivine-rich Tok peridotites typically has convex-upward trace element patterns (La/Nd_PM < 1 and Nd/Yb_PM ? 1), which we consider as evidence for equilibration with evolved silicate liquids (with higher REE and lower Ti contents than in host basalts). Whole-rock patterns of the olivine-rich xenoliths range from convex-upward to LREE-enriched (La/Nd_PM > 1); the LREE-enrichments are positively correlated with phosphorus abundances and are mainly hosted by accessory phosphates and P-rich cryptocrystalline materials. In addition to apatite, some Tok xenoliths contain whitlockite (an anhydrous, halogen-poor and Na-Mg-rich phosphate), which is common in meteorites and lunar rocks, but has not been reported from any terrestrial mantle samples. Some olivine-rich peridotites have generations of clinopyroxene with distinct abundances of Na, LREE, Sr and Zr. The mineralogical and trace element data indicate that the lithospheric mantle section represented by the xenoliths experienced a large-scale metasomatic event produced by upward migration of mafic silicate melts followed by percolation of low-T, alkali-rich melts and fluids. Chromatographic fractionation and fractional crystallisation of the melts close to the percolation front produced strong LREE-enrichments, which are most common in the uppermost mantle and are related to carbonate- and P₂O₅-rich derivatives of the initial melt. Reversal and gradual retreat of the percolation front during thermal relaxation to ambient geotherm (“retrograde” metasomatism) caused local migration and entrapment of small-volume residual fluids and precipitation of volatile-rich accessory minerals. A distinct metasomatic episode, which mainly produced “anhydrous” late-stage interstitial materials was concomitant with the alkali basaltic magmatism, which brought the xenoliths to the surface.     

Geochemistry and geochronology of mafic rocks from Bamenda Mountains (Cameroon): Source composition and crustal contamination along the Cameroon Volcanic Line

Mafic rocks from the Bamenda volcanic province along the Cameroon Volcanic Line have been dated from 17 to 0 Ma. Associated with some trachytes and rhyolites, this volcanism covers a period of more than 25 Ma. The studied rocks are basalts to mugearites. Most of them have been contaminated by continental crust during their transit to the surface. The oldest rocks are the most contaminated. One group of samples shows high Eu, Sr and Ba contents. This characteristic is not due to crustal contamination process, but has a mantle source origin. We argue that these characteristics have been acquired by mixing of melts formed by partial melting of mantle pyroxenites with melts formed in mantle peridotites. Such pyroxenites have been observed as mantle xenoliths in the Adamaoua province, and their chemical and isotopic compositions are consistent with such a model.     

Late Pleistocene and Holocene activity of the Atacazo–Ninahuilca Volcanic Complex (Ecuador)

The Atacazo–Ninahuilca Volcanic Complex (ANVC) is located in the Western Cordillera of Ecuador, 10 km southwest of Quito. At least six periods of Pleistocene to Holocene activity (N1 to N6) have been preserved in the geologic record as tephra fallouts and pyroclastic flow deposits. New field data, including petrographic and whole-rock geochemical analyses of over forty soil and tephra sections, 100 pumice and lithic samples, and 10 new ¹⁴C ages allow us to constrain: (1) the tephra fall isopachs and detailed characteristics of the last two events (N5–N6) including volume estimates of the tephra and pyroclastic flow deposits and the corresponding volcanic explosivity index (VEI); (2) the petrographical and geochemical correlations between domes, tephras, and pyroclastic flow deposits; and, (3) the timing of the last 4 eruptive events and a period of quiescence that endured a few thousand years (1000–4000).     

L'hétérogénéité du manteau supérieur à l'aplomb du volcan de Nyos (Cameroun) révélée par les enclaves ultrabasiques

Volcanic deposits from the lake Nyos (Cameroon) contain ultrabasic xenoliths: lherzolites, harzburgites and websterites, sometimes containing amphibole. Major and trace element compositions of clinopyroxene and amphibole allow the recognition of an old depletion event followed by two episodes of incompatible-element enrichment. One is high in light rare-earth elements, while the other one is low in these elements, but high in U and Th. Their relative chronology is not yet established. To cite this article: R. Temdjim et al., C. R. Geoscience 336 (2004).