Discrete zircons, up to 9 mm in length, occur in alluvial deposits from the Veneto area. They are likely derived from the disaggregation of lamprophyric rocks belonging to a regional, pervasive dyke-swarm. Zircon and REE phases occur in both alkaline lamprophyres and connate calcite-bearing felsic lithics and their debris in lamprophyre breccia. We present 36 new complete U–Pb and trace element analyses of zircons and associated inclusions. We used a statistical approach on a larger dataset using new and literature data to evaluate the confidence figure to give an estimation of age of zircons. Inclusions suggest a genetic link with an S–CO₂–ZrO–BaO–SrO–CaO-rich fluid/melt possibly associated with carbonate-rich alkaline parental magma and a metasomatised mantle source. This paper confirms the importance of calcite–syenite and lamprophyre genetic link and zircon magmatic origin, in contrast with hydrothermal and metamorphic zircons. U–Pb dating by LA-ICP-MS provides time constrains (40.5–48.4 Ma, Lutetian), consistent with the age of the alkaline magmatic event. Trace element data indicate a link to anorogenic magmatism associated with mantle upwelling. Complex zoning is highlighted by cathodoluminescence images. The Veneto zircons are helpful for regional geological information and may have commercial potential as a critical resource for green technologies.

We investigated hellandite-group mineral phases from the Roman Region, alkali syenite ejecta, by multimethod analyses. They show a complex crystallisation history including co-precipitation of hellandite-(Ce) with brockite, resorption, sub-solidus substitution with mottanaite-(Ce), exsolution of perthite-like ferri-mottanaite-(Ce), overgrowth of an oscillatory-zoned euhedral shell of ferri-mottanaite-(Ce) and late, secondary precipitation of pyrochlore in the cribrose hellandite-(Ce) core. LREE/HREE crossover and a negative Eu anomaly in hellandite-group minerals follows fO₂ increase during magma cooling. The distinction among the hellandite-group minerals is based on the element distribution in the M1, M2, M3, M4 and T sites. Additional information on miscibility relationship among the hellandite sensu strictu, tadzhikite, mottanaite, ferri-mottanaite and ciprianiite endmembers derives from molar fraction calculation. We observed that change in composition of hellandite-group minerals mimic the ligands activity in carbothermal-hydrothermal fluids related to carbonatitic magmatism.