Trace element behaviour during interaction between basalt and crustal rocks at 0.5–0.8 GPa: an experimental approach

We experimentally investigate the major and trace elements behavior during the interaction between two partially molten crustal rocks (meta-anorthosite and metapelite) and a basaltic melt at 0.5–0.8 GPa. Results show that a hybrid melt is formed at the basalt-crust contact, where plagioclase crystallizes. This contact layer is enriched in trace elements which are incompatible with plagioclase crystals. Under these conditions, the trace element diffusion coefficients are one order of magnitude larger than those expected. Moreover, the HFSE diffusivity in the hybrid melt is surprisingly higher than the REE one. Such a feature is related to the plagioclase crystallization that changes the trace elements liquid-liquid partitioning (i.e. diffusivity) over a transient equilibrium that will persist as long as the crystal growth proceeds. These experiments suggests that the behaviour of the trace elements is strongly dependent on the crystallization at the magma-crust interface. Diffusive processes like those investigated can be invoked to explain some unusual chemical features of contaminated magmatic suites.     

Carbonate assimilation in magmas: A reappraisal based on experimental petrology

The main effect of magma–carbonate interaction on magma differentiation is the formation of a silica-undersaturated, alkali-rich residual melt. Such a desilication process was explained as the progressive dissolution of CaCO₃ in melt by consumption of SiO₂ and MgO to form diopside sensu stricto. Magma chambers emplaced in carbonate substrata, however, are generally associated with magmatic skarns containing clinopyroxene with a high Ca-Tschermak activity in their paragenesis. Data are presented from magma–carbonate interaction experiments, demonstrating that carbonate assimilation is a complex process involving more components than so far assumed. Experimental results show that, during carbonate assimilation, a diopside–hedenbergite–Ca-Tschermak clinopyroxene solid solution is formed and that Ca-Tschermak/diopside and hedenbergite/diopside ratios increase as a function of the progressive carbonate assimilation. Accordingly, carbonate assimilation reaction should be written as follows, taking into account all the involved magmatic components:CaCO₃^solid + SiO₂^melt + MgO^melt + FeO^melt + Al₂O₃^melt → (Di–Hd–CaTs)_ss^solid + CO₂^fluidThe texture of experimental products demonstrates that carbonate assimilation produces three-phases (solid, melt, and fluid) whose main products are: i) diopside–hedenbergite–Ca-Tschermak clinopyroxene solid solution; ii) silica-undersaturated CaO-rich melt; and iii) C–O–H fluid phase. The silica undersaturation of the melt and, more importantly, the occurrence of a CO₂-rich fluid phase, must be taken into account as they significantly affect partition coefficients and the redox state of carbonated systems, respectively.     

Dependence of clinopyroxene composition on cooling rate in basaltic magmas: Implications for thermobarometry

The compositional variation of clinopyroxene and the partitioning of major elements between clinopyroxene and melt are estimated as a function of the cooling rate. Clinopyroxenes were crystallized under variable cooling regimes (15, 9.4, 3, 2.1, and 0.5 °C/min from 1250 down to 1000 °C) and at isothermal conditions of 1000 °C from a basaltic composition at a pressure of 500 MPa under anhydrous and hydrous (H₂O = 1.3 wt.%) conditions. The clinopyroxene chemistry shows that, as the cooling rate increases, crystals are progressively depleted in Ca, Mg, Fe²⁺ and Si and enriched in Na, Fe³⁺, Al (mainly Al^IV), and Ti. Di and Hd versus CaTs and CaFeTs form a continuous binary solid solution characterized by higher amounts of tschermakitic components with increasing cooling rate. Two parameters (DH = Di + Hd and TE = CaTs + CaFeTs + En) are calculated to describe the effect of cooling rate on the clinopyroxene composition. The variation of DH/TE with increasing cooling rate evidences the kinetic process induced by rapid cooling in basic rocks under hydrous and anhydrous conditions.Dynamic crystallization conditions affect the partitioning of major elements between clinopyroxene and melt; with increasing cooling rate, the value of crystal–melt partition coefficient departs from that obtained at the isothermal condition. However, in spite of these variations, the values of ^cpx–meltKd_Fe–Mg remain almost constant. Therefore, the Fe²–Mg exchange between clinopyroxene and melt is not suitable to prove the (dis)equilibrium conditions in basaltic cooling magmas, giving rise to possible mismatches in the application of thermobarometers. The results of our study are consistent with that observed at the margin of dikes or in the exterior portions of lavas, where the cooling rate is maximized and disequilibrium compositions of clinopyroxene have been found.     

Time-dependent geochemistry of clinopyroxene from the Alban Hills (Central Italy): Clues to the source and evolution of ultrapotassic magmas

We investigated chemical and isotopic compositions of clinopyroxene crystals from well age-constrained juvenile scoria clasts, lava flows, and hypoabyssal magmatic ejecta representative of the whole eruptive history of the Alban Hills Volcanic District. The Alban Hills is a Quaternary ultra-potassic district that was emplaced into thick limestone units along the Tyrrhenian margin of Italy. Alban Hills volcanic products, even the most differentiated, are characterised by low SiO₂ content. We suggest that the low silica activity in evolving magmas can be ultimately due to a decarbonation process occurring at the magma/limestone interface. According to the liquid line of descent we propose, the differentiation process is driven by crystallisation of clinopyroxene + leucite ± apatite ± magnetite coupled with assimilation of a small amount of calcite and/or with interaction with crustal CO₂. By combining age, chemical data, strontium and oxygen isotopic compositions, and REE content of clinopyroxene, we give insights into the evolution of primitive ultrapotassic magmas of the Alban Hills Volcanic District over an elapsed period of about 600 kyr. Geochemical features of clinopyroxene crystals, consistent with data coming from other Italian ultrapotassic magmas, indicate that Alban Hills primary magmas were generated from a metasomatized lithospheric mantle source. In addition, our study shows that the ⁸⁷Sr / ⁸⁶Sr and LREE/HREE of Alban Hills magmas continuously diminished during the 600–35 ka time interval of the Alban Hills eruptive history, possibly reflecting the progressive depletion of the metasomatized mantle source of magmas.     

Predictive assessment of the asbestos content in the Western Italian Alps: an essential tool for an effective approach to risk analysis and management in tunneling operations and muck reuse

The modern approach to the design and management of tunnel excavation, and muck reuse, can be influenced to a great extent by the possible presence of rock formations containing asbestos minerals. This situation creates problems concerning the protection of the workers’ health and the expectable environmental criticalities, while a drastic re-consideration of the muck destination is necessary. Since, in the case of carcinogens, corrective action following exposure or dispersion is not acceptable, detailed knowledge of the characteristics of the material to be excavated is all the more essential. Only on this basis it is possible to design the tunneling operations in a prevention through design approach, so that the tunnel driving techniques, fittings and technologies, and special equipment and modus operandi, can grant, where necessary, minimized risk conditions, and make a correct decision on whether, how and when these measures must be fully activated, since such an approach involves a remarkable impact on costs and work organization. In the Western Alps a detailed identification and quantification of the asbestos content in rocks is a difficult task, due to the fact that the asbestos in the host rocks, mainly serpentinite, shows a highly variable distribution, typical of ophiolitic belts throughout the world, as it is mostly associated with joints and shear zones. The possibilities of a predictive assessment of the asbestos content in the formations to be excavated are here discussed, with special reference to the reliability of the achievable results.     

Sulfur diffusion in basaltic melts

We measured the diffusion coefficients of sulfur in two different basaltic melts at reduced conditions (i.e., in the sulfide stability field), temperatures from 1225°C to 1450°C, pressures of 0.5 and 1 GPa, and water concentrations of 0 and 3.5 wt%. Although each melt is characterized by slightly different sulfur diffusion coefficients, the results can be combined to create a general equation for sulfur diffusion in anhydrous basalts:

     

Endogenous and nonimpact origin of the Arkenu circular structures (al‐Kufrah basin—SE Libya)

Abstract– The twin Arkenu circular structures (ACS), located in the al‐Kufrah basin in southeastern Libya, were previously considered as double impact craters (the “Arkenu craters”). The ACS consist of a NE (Arkenu 1) and a SW structure (Arkenu 2), with approximate diameters of about 10 km. They are characterized by two shallow depressions surrounded by concentric circular ridges and silica‐impregnated sedimentary dikes cut by local faults. Our field, petrographic, and textural observations exclude that the ACS have an impact origin. In fact, we did not observe any evidence of shock metamorphism, such as planar deformation features in the quartz grains of the collected samples, and the previously reported “shatter cones” are wind‐erosion features in sandstones (ventifacts). Conversely, the ACS should be regarded as a “paired” intrusion of porphyritic stocks of syenitic composition that inject the Nubia Formation and form a rather simple and eroded ring dike complex. Stock emplacement was followed by hydrothermal activity that involved the deposition of massive magnetite–hematite horizons (typical of iron oxide copper‐gold deposits). Their origin was nearly coeval with the development of silicified dikes in the surroundings. Plugs of tephritic‐phonolitic rocks and lamprophyres (monchiquites) inject the Nubian sandstone along conjugate fracture zones, trending NNW–SSE and NE–SW, that crosscut the structural axis of the basin.