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Mantle magmas interact with surrounding rocks during their ascent and storage in the continental crust, leading to open system processes as wall rock partial melting. In this study, we have experimentally investigated the reactions between a leucosome depleted migmatite and a primitive K-basaltic of Campi Flegrei (Italy). Experiments were carried out at pressure of 0.8 GPa temperatures from 1250 °C to 1050 °C and constant temperature and thermal gradient conditions. The experimental products consist of biotite-free migmatite, glass and crystals of clinopyroxene, olivine, plagioclase and Cr-spinel with proportions that vary as a function of temperature. Open system isothermal experiments indicate that the chemistry of melts and phase relationships are controlled by the high Al2O3 content of leucosome depleted migmatite with the glass composition shifting from K-trachybasalt towards shoshonite as the temperature decreases from 1200 °C to 1125 °C. At temperatures 1150°C, migmatite assimilation is not exclusively due to the assimilation fractional crystallization process because evidence of mingling and mixing is observed. T-gradient experiment shows melt composition ranging from shoshonite to phono-tephrite moving from the slightly crystalline zone (T = 1250 –1210 °C) at the bottom of the capsule towards the highly crystalline zone (T = 1160 –1140 °C). This SiO2-constant trend indicates that at temperature below the basalt solidus, the assimilation of leucosome depleted crust is represented almost exclusively by the biotite breakdown, leading to the increase in Al, Mg, Fe, Ti, and K activities in the system. The shoshonitic composition obtained in our experiments could represent the parental magma for both Campi Flegrei volcanic district and Vesuvius magmatic systems, indicating modification in a deep storage zone through mixing with the partial melts derived from restitic continental crust.

Time-series experiments were carried out in a piston-cylinder apparatus at 0.8 GPa and 1030-1080 °C using a hydrous K-basalt melt as the starting material to determine the element partition coefficients between amphibole and silicate glass. Major, minor, and trace element compositions of amphibole and glass were determined with a combination of electron microprobe and laser ablation inductively coupled plasma mass spectrometry. Results show that the main mineral phase is calcic amphibole, and the coexisting glass compositions range from basaltic trachyandesite to andesite. We estimated the ideal radius, the maximum partition coefficient and the apparent Young's modulus of the A, M1-M2-M3, and M4-M4′ sites of amphibole. The influence of melt and amphibole composition, temperature, and pressure on the partition coeficients between amphiboles and glasses has also been investigated by comparing our data with a literature data set spanning a wide range of pressures (0.6-2.5 GPa), temperatures (780-1100 °C), and compositions (from basanite to rhyolite). Finally, we modeled a deep fractional crystallization process using the amphibole-melt partition coeficients determined in this study, observing that significant amounts of amphibole crystallization (>30 wt%) well reproduce the composition of an andesitic melt similar to that of the calc-alkaline volcanic products found in Parete and Castelvolturno boreholes (NW of Campi Flegrei, Italy).

Time-series crystallization/dissolution experiments were conducted on a natural potassic basalt seeded with bytownitic plagioclases (Plg) at atmospheric pressure, in air, at 1180-1240 °C and isothermal dwell time up to 20 hours. Plg-seed presence promotes the early formation of new-Plg, dampening the clinopyroxene (Cpx) crystallization. New-Plgs grow at a rate from 10-6 up to 10-8 cm·s-1 as the dwell time increases. Seeds overgrow at similar rate. Cpx crystallizes with a delay of at least 3 hours; this has a significant impact on the composition of both residual melt and new-Plgs. For undercooling >35 °C the Cpx delay causes a strong supersaturation of this phase in the melt resulting in a decrease in the new-Plg nucleation rate by 2 orders of magnitude in the 3 h-experiment. In the 15h-run, Cpx coarsening and the decrease of crystallinity suggest the achievement of a near-equilibrium conditions. Cpx growth rate is in the order of 10-7 cm·s-1 showing very limited variation. Finally, for the investigated superheating (5-15 °C) only the long lasting experiments allows an estimation of Plg dissolution rate (10-9 cm·s-1) although changes in the melt composition are already detectable in the 3h-runs. As a whole our results suggest that in natural systems, the takeover of antecrysts/ xenocrysts by a magma can induce on a short time scales, changes in its initial nucleation behavior with remarkable petrological implications for the solidification paths and eruptive dynamics of potassic magmatic systems.

The study of the oxidation state of lithospheric mantle-derived rocks allows modelling the deep cycle of volatiles (e.g., C, H, O, N and S) in the Earth's interior, which in turn plays a role in magma genesis, metasomatism and volcanic degassing. At the oxygen fugacity (i.e., fO2) recorded by residual abyssal peridotites, volatile elements like carbon are predicted to be in the immobile form of graphite. However, the compilation of the redox state of worldwide-distributed continental xenoliths shows evidence of their oxidation and refertilization through time by deeply formed subduction-related metasomatic fluids. The analyses of fluid inclusions in mantle-derived minerals like olivine (or pyroxenes) represent a snapshot of the volatile circulation in depth, whose noble gases signature (He, Ar, Ne) is used to identify their possible source. This study aims to reconstruct the origin of mantle metasomatism underneath the Hyblean Plateau (Sicily, Italy) and its redox history through the investigation of spinel-peridotite nodules, combining fO2 estimates with noble gases and fluid inclusions chemistry from hand-picked olivine grains. We analyzed eight mantle xenoliths classified as spinel lherzolites and spinel harzburgites from the Valle Guffari (Hyblean Plateau, Sicily). The calculated logfO2 is higher than that of most cratonic xenoliths worldwide ranging between 0.28 and 1.27 log units above to the fayalite-magnetite-quartz (FMQ) reference buffer. Micro-Raman measurements on olivine grains with dendritic trails of (metasomatic) fluid inclusions reveal an assemblage made of Mg-Ca carbonates ± sulfide ± elemental sulfur ± CO2 in the most reduced sample, and Mg-Ca carbonates ± sulfates ± CO2 in the most oxidized sample, the latter associated with a silicate glass and (secondary) hydrous phases. Both assemblages are taken as evidence of the product of crystallization of deeply originated volatile-bearing silicate melts. Analyses of He, Ar, and Ne in olivine grains confi

We present new experimental data on major and trace element partition coefficients (D) between clinopyroxene and a K-basaltic melt from Procida Island (Campi Flegrei Volcanic District, south Italy). Time-series experiments were conducted at 0.8 GPa and 1080–1250 °C aiming to investigate the role of the crystallization kinetics on trace elements partitioning behaviour at a pressure relevant for deep magmatic reservoirs. Results indicate that large ion lithophile elements (LILE) are incompatible (e.g., DSr ≤ 0.15), light rare elements (LREE; e.g., DLa ≤ 0.20) are always more incompatible than heavy rare elements (HREE), which in some cases result to be compatible with clinopyroxene (e.g., DDy = 1.40); high field strength elements (HFSE) are generally incompatible (DHFSE ≤ 0.8), while transition elements (TE) range from slightly incompatible (e.g., DV = 0.6) to highly compatible (e.g., DCr = 63). The calculated D values for LILEs, REEs, HFSEs, and TEs tend to decrease with the increase of temperature and to increase with increasing tetrahedrally-coordinated aluminium content, in agreement with the previous studies. Moreover, we observed the influence of the growth rate on the partition coefficients, with the highest DREE values calculated in the runs with the highest growth rate (~10−7 cm s−1), due to the less efficient rejection of incompatible elements during rapid crystal growth, that in this study is not linked to disequilibrium conditions, but to the presence of pre-existing nuclei. Additionally, the apparent increase in DREE values with time observed in some runs is not referable to a change in time but rather to the different degrees of polymerization, expressed as the ratios NBO/T of these melts, strictly related to a loss of Fe occurred during the experiments, and thus to a different melt viscosity. Finally, the application of the experimental clinopyroxene-melt partition coefficients highlights that the deepest step of the magmatic differentiation in the Camp

Dissolution of clinopyroxene (cpx) in a K-basaltic melt from the Campi Flegrei Volcanic District (Italy) has been investigated through dissolution and dissolution-crystallization experiments at pressure of 0.8 GPa, superliquidus temperature of 1350 °C, and dwell times between 0.5 and 1 h. The obtained dissolution rates range from 7.9·10−6 cm s−1 to 6.1·10−6 cm s−1 as a function of dwell time. In the dissolution-crystallization experiment (1300 °C; 0.8 GPa; 2 h), the formation of overgrowth rims accompanied by new cpx crystals suggests that the injection of recharge magmas in basaltic reservoir may lead to inverse or oscillatory zonation. The interaction between cpx and K-basaltic melt at ~1570 °C was studied by in situ radiography using synchrotron radiation combined with the Paris-Edinburgh press. This resulted in cpx resorption to occur depending on the temperature conditions with respect to the liquidus temperature of the cpx (TcpxL). The calculated cpx dissolution rates are ~5·10−3 cm s−1 at T ≤ TcpxL and ~ 3·10−2 cm s−1 at T ≥ TcpxL. The role of crystal dissolution in the estimation of magma residence times has been also tested for a natural magmatic system by interpolating the dissolution rates (~10−5–10−6 cm s−1) with the textural data of cpx phenocrysts from the Agnano-Monte Spina pyroclastic deposit at Campi Flegrei caldera (Campanian region, Italy). Results from calculations indicate that the time required for partial or complete resorption of phenocrysts varies from ~0.5 to ~40 h, and that the effect of crystal dissolution may be relevant to estimate magma residence times whether significant dissolution occurs during magma mixing processes.

Amphibole growth rates were experimentally determined at hydrous (3.3–4.2 wt% H2O), isobaric (0.8 GPa) conditions, variable temperature (1030 and 1080 °C) and dwell time (0.25, 3, 6, and 9 h), using as starting material a primitive alkaline basalt from Procida island (Campi Flegrei Volcanic District, south Italy). Amphibole growth rates decrease from 1.5·10−7 to 2.9·10−8 cm s−1 as the duration of the experiments increase from 0.25 to 9 h. Moreover, increasing both temperature and water content leads to similar growth rate increase at constant dwell time. The comparison between amphibole and clinopyroxene growth rates determined at the same experimental conditions reveals for amphibole a faster growth relatively to the coexisting clinopyroxene, regardless of the dwell time. Furthermore, the experimental time appears to be a critical parameter for the composition of synthetic amphiboles; specifically, edenite is the dominant composition in short experiments (≤3 h), particularly, at low temperature (1030 °C), whereas the magnesiohastingsitic amphibole becomes progressively more important shifting towards longer duration and higher temperature run conditions. The magnesiohastingsite, on the basis of the amphibole-liquid Fe-Mg exchange coefficient values, results to be the compositional term representative of amphibole-melt equilibrium at the investigated P-T-H2O conditions. Finally, experimental growth rates from this study have been used to investigate the crystallization time of natural amphiboles and clinopyroxenes from the Oligo-Miocene cumulates of north-western Sardinia (i.e. Capo Marargiu Volcanic District, Italy), yielding crystallization times of 1.46–3.12 yr.