The occurrence of carbonatites in oceanic settings is very rare if compared with their continental counterpart, having been reported only in Cape Verde and Canary Islands. This paper provides an overview of the main geochemical characteristics of oceanic carbonatites, around which many debates still exist regarding their petrogenesis. We present new data on trace elements in minerals and whole-rock, together with the first noble gases isotopic study (He, Ne, Ar) in apatite, calcite, and clinopyroxene from Fuerteventura carbonatites (Canary Islands). Trace elements show a similar trend as Cape Verde carbonatites, almost tracing the same patterns on multi-element and REE abundance diagrams. ³He/⁴He isotopic ratios of Fuerteventura carbonatites reflect a shallow (sub-continental lithospheric mantle, SCLM) He signature in their petrogenesis, and they clearly differ from Cape Verde carbonatites, i.e., fluids from a deep and low degassed mantle with a primitive plume-derived He signature are involved in their petrogenesis.

We investigated the carbon isotope composition of mantle source beneath the Hyblean Plateau (southeast Sicily, Italy) by studying CO₂ in fluid inclusions from ultramafic xenoliths recovered in some Miocene diatremes. In order to constrain the processes influencing the isotopic marker of carbon we combined δ¹³C_CO2 results with information about noble gases (He and Ar) obtained in a previous investigation of the same products. Although Ar/CO₂ and He/Ar ratios provide evidence of Rayleigh-type fractional degassing, the isotopic geochemistry of carbon is poorly influenced by this process. Mixing related to metasomatic processes where MORB-type pyroxenitic melts permeate a peridotite mantle probably contaminated by crustal fluids inherited from a fossil subduction can explain the measured δ¹³C and CO₂/³He variations, ranging from −4‰ to −2‰ and from 10⁹ to 10¹⁰, respectively. Simple mass-balance calculations highlighted that the Hyblean peridotite source was mainly contaminated by the carbonate source, being carbonate and organic matter present at a ratio that varied within the range from 7:1 to 4:1.

Ultramafic magmas (MgO ≥ 18 wt%) are generally thought to be primary mantle melts formed at temperatures in excess of 1600 °C. Volatile contents are expected to be low, and accordingly, high-Mg magmas generally do not yield large explosive eruptions. However, there are important exceptions to low explosivity that require an explanation. Here we show that hydrous (hence, potentially explosive) ultramafic magmas can also form at crustal depths at temperatures even lower than 1000 °C. Such a conclusion arose from the study of a silicate glass vein, ~1 mm in thickness, cross-cutting a mantle-derived harzburgite xenolith from the Valle Guffari nephelinite diatreme (Hyblean area, Sicily). The glass vein postdates a number of serpentine veins already existing in the host harzburgite, thus reasonably excluding that the melt infiltrated in the rock at mantle depths. The glass is highly porous at the sub-micron scale, it also bears vesicles filled by secondary minerals. The distribution of some major elements corresponds to a meimechite composition (MgO = 20.35 wt%; Na₂O + K₂O < 1 wt%; and TiO₂ > 1 wt%). On the other hand, trace element distribution in the vein glass nearly matches the nephelinite juvenile clasts in the xenolith-bearing tuff-breccia. These data strongly support the hypothesis that an upwelling nephelinite melt (MgO = 7–9 wt%; 1100 ≤ T ≤ 1250 °C) intersected fractured serpentinites (T ≤ 500 °C) buried in the aged oceanic crust. The consequent dehydroxilization of the serpentine minerals gave rise to a supercritical aqueous fluid, bearing finely dispersed, hydrated cationic complexes such as [Mg²⁺(H₂O)_n]. The high-Mg, hydrothermal solution "flushed" into the nephelinite magma producing an ultramafic, hydrous (hence, potentially explosive), hybrid magma. This hypothesis explains the volcanological paradox of large explosive eruptions produced by ultramafic magmas.

This study focus on the Mt Etna December 2018 eruption with the aim of investigating the geochemical characteristics of the feeding magma. New data on major and trace element geochemistry of olivine-hosted melt inclusions (MI) in volcanic products are presented together with the noble gas geochemistry of fluid inclusions (FI) in olivines. The noble gas geochemistry of fluid inclusions (FIs) in olivines was also investigated. The major element composition of MIs is variable from tephrite/trachybasalt to phonotephrite/basaltic trachyandesite, with SiO₂ = 45.51–52.72 wt%, MgO = 4.01–6.02 wt%, and CaO/Al₂O₃ = 0.34–0.72. Trace element patterns of MIs present a typical enrichment in LILE and LREE, depletion in HFSE, and relatively fractionated REE patterns: (La/Lu) N= 18.8–41.08, with Eu/Eu* = (0.5–1.8). Positive anomalies in Sr (Sr/Sr* = 0.8–2.3) and Ba can be ascribed to the assimilation of plagioclase-rich cumulates in the magmatic reservoir. The variable Ba/La (9.8–15.8), K/Nb (260–1037), Ce/Nb (1.9–3.4), Rb/La (0.4–1.6), and Ba/Nb (10.8–25.8) ratios reveal mixing between two types of end-member magmas comparable to those emitted from 1) the 2001 Upper Vents and 2002–03 Northern Fissures (Type-1) and 2) the 2001 Lower Vents and 2002–03 Southern Fissures (Type-2), respectively. Type-2 represents a magma that was under the influence of a crustal component, whereas Type-1 is compatible with a HIMU–MORB-type heterogeneous mantle source. It appears that the 2018 MIs have captured the two different types of magmas, and the lack of homogenization may imply a very fast ascent (a few months). Compatible with the contemporary presence of primordial HIMU–MORB and crust-contaminated end-members are the data on noble gases from FI that highlighted an ³He/⁴He value of 6.5–6.6Ra. The hypothesis of two different types of magmas, identified by the trace element geochemistry in MIs, is, thus, reinforced by helium isotopic data on FI of the 2018 eruption together with data from other Etnean eruptions and allows the inference of a bicomponent magma mixing.