Contrasting radon background levels in volcanic settings: clues from 220Rn activity concentrations measured during long-term deformation experiments

To better understand the mechanisms leading to different radon background levels in volcanic settings, we have performed two long-term deformation experiments of 16 days using a real-time setup that enables us to monitor any variation of radon activity concentration during rock compression. Our measurements demonstrate that, in the case of highly porous volcanic rocks, the emanating power of the substrate changes as a function of the volcanic stress conditions. Constant magmatic pressures, such as those observed during dike intrusions and hydrothermal fluid injections, can result in pervasive pore collapse that is mirrored by a significant radon decrease until a constant emanation is achieved. Conversely, repeated cycles of stress due to, for example, volcano inflation/deflation cycles, cause a progressive radon increase a few days (but even weeks and months) before rupture. After rock failure, however, the formation of new emanation surfaces leads to a substantial increase of the radon signal. Our results suggest that surface deformation in tectonic and volcanic settings, such as inflation/deflation or constant magmatic pressures, have important repercussions on the emanating power of volcanic substrates.     

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.     

Magma–carbonate interaction: An experimental study on ultrapotassic rocks from Alban Hills (Central Italy)

The Alban Hills ultrapotassic volcanic district is one of the main districts emplaced during Quaternary time along the Tyrrhenian margin of Italy. Alban Hills lava flows and scoria clasts are made up essentially of clinopyroxenes and leucites and their chemical composition is mostly K-foiditic. Differentiated products (MgO < 3 wt.%) are characterised by low SiO₂ concentration (< 50 wt.%) and geochemical features indicate that this unique differentiation trend is driven by crystal fractionation plus carbonate crust interaction. Notably, the Alban Hills Volcanic District was emplaced into thick limestone units. With the aim of constraining the magmatic differentiation, we performed experiments on the Alban Hills parental composition (plagioclase-free phono-tephrite) under anhydrous, hydrous, and hydrous-carbonated conditions. Experiments were carried out at 1 atm, 0.5 GPa and 1 GPa, temperatures ranging from 1050 to 1300 °C, and H₂O and CaCO₃ in the starting material up to 2 and 7 wt.%, respectively. The experiments performed at 0.5 GPa are the most representative of the Alban Hills plumbing system. Clinopyroxene and leucite are the main phases occurring under all the investigated conditions and the liquidus phases. Nevertheless, our experimental results demonstrate that the occurrence of CaCO₃ in the starting material strongly affects phase relations. Experiments performed under hydrous conditions crystallize magnetite and phlogopite at relatively high temperature. This early crystallization drives the glass composition towards a silica enrichment, resulting in a differentiation trend moving from phono-tephritic (Alban Hills parental composition) to phonolitic compositions. This is in contrast with micro-textural evidence showing late crystallization of magnetite and phlogopite in the natural products and with the composition of the juvenile products. On the contrary, in the CaCO₃-bearing experiments (i.e., simulating magma–carbonate interaction) the magnetite and phlogopite stability fields are strongly reduced. As a consequence, the melt differentiation is mainly controlled by the cotectic crystallization of clinopyroxene and leucite, resulting in a differentiation trend moving towards K-foiditic compositions. These experimental results are in agreement with micro-textural features and chemical compositions of Alban Hills natural products and with the magmatic differentiation model inferred by geochemical data. Magma–carbonate interaction is not a rare process and its occurrence has been demonstrated for different plumbing systems. However, the uniqueness of the Alban Hills liquid line of descent suggests that the efficacy of the carbonate contamination process is controlled by different factors, the dynamics of the plumbing system being one of the most important.     

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.     

Deformation and fluid flow during orogeny at the palaeo-Pacific active margin of Gondwana: the Early Palaeozoic Robertson Bay accretionary complex (north Victoria Land, Antarctica)

Structural investigations, integrated with X‐ray diffraction, fluid inclusion microthermometry and oxygen‐stable isotope analyses are used to reconstruct the deformation history and the palaeo‐fluid circulation during formation of the low‐grade, turbidite‐dominated Early Palaeozoic Robertson Bay accretionary complex of north Victoria Land (Antarctica). Evidence for progressive deformation is elucidated by analysing the textural fabric of chronologically distinct, thrust‐related quartz vein generations, incrementally developed during progressive shortening and thickening of the Robertson Bay accretionary complex. Our data attest that orogenic deformation was mainly controlled by dissolution–precipitation creep, modulated by stress‐ and strain‐rate‐dependent fluid pressure cycling, associated with local and regional permeability variations induced by the distribution and evolution of the fracture network during regional thrusting. Fracture‐related fluid pathways constituted efficient conduits for episodic fluid flow. The dominant migrating fluid was pre‐to‐syn‐folding and associated with the migration of warm (160–200 °C) nitrogen‐ and carbonic (CO₂ and CH₄)‐bearing fluids. Both fluid advection and diffusive mass transfer are recognized as operative mechanisms for fluid–rock interaction and vein formation during continuous shortening. In particular, fluid–rock interaction was the consequence of dissolution–precipitation creep assisted by tectonically driven cooling fluids moving through the rock section as a result of seismic pumping. The most likely source of the migrating fluids would be the frontal part of the growing accretionary complex, where fluids from the deep levels in the hinterland are driven trough channelization operated by the thrust‐related fracture (fault) systems.     

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.     

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.     

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.     

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.