Abstract Both silicate melts and aqueous fluids are thought to play critical roles in the chemical differentiation of the Earth's crust and mantle. Yet their relative effects are poorly constrained. We have addressed this issue by measuring partition coefficients for 50 trace and minor elements in experimentally produced aqueous fluids, coexisting basanite melts, and peridotite minerals. The experiments were conducted at 1.0–4.0 GPa and 950–1200°C in single capsules containing (either 40 or 50 wt %) H 2 O and trace element‐enriched basanite glass. This allowed run products to be easily identified and analyzed by a combination of electron microprobe and LAM‐ICP‐MS. Fluid and melt compositions were reconstructed from mass balances and published solubility data for H 2 O in silicate melts. Relative to the basanite melt, the solutes from H 2 O‐fluids are enriched in SiO 2 , alkalis, Ba, and Pb, but depleted in FeO, MgO, CaO, and REE. With increasing pressure, the mutual solubility of fluids and melts increases rapidly with complete miscibility between H 2 O and basanitic melts occurring between 3.0 and 4.0 GPa at 1100°C. Although LREE are favored over HREE in the fluid phase, they are less soluble than the HFSE (Nb, Ta, Zr, Hf, and Ti). Thus, the relative depletions of HFSE that are characteristic of arc magmas must be due to a residual phase that concentrates HFSE (e.g., rutile). Otherwise, H 2 O‐fluids have the capacity to impart many of the geochemical characteristics that distinguish some rocks and melts from the deep mantle lithosphere (e.g., MARID and lamproites).
Laser ablation ICP-MS enables streamlined, high-sensitivity measurements of rare earth element (REE) abundances in geological materials. However, many REE isotope mass stations are plagued by isobaric interferences, particularly from diatomic oxides and argides. In this study, we compare REE abundances quantitated from mass spectra collected with low-resolution (m/Δm = 300 at 5% peak height) and medium-resolution (m/Δm = 2500) mass discrimination. A wide array of geological samples was analyzed, including USGS and NIST glasses ranging from mafic to felsic in composition, with NIST 610 employed as the bracketing calibrating reference material. The medium-resolution REE analyses are shown to be significantly more accurate and precise (at the 95% confidence level) than low-resolution analyses, particularly in samples characterized by low (<μg/g levels) REE abundances. A list of preferred mass stations that are least susceptible to isobaric interferences is reported. These findings impact the reliability of REE abundances derived from LA-ICP-MS methods, particularly those relying on mass analyzers that do not offer tuneable mass-resolution and/or collision cell technologies that can reduce oxide and/or argide formation. Graphical Abstract ᅟ.
Abstract The lower crustal domain of the Ivrea‐Verbano Zone (NW Italy) hosts five ~300‐m‐wide pipe‐like ultramafic intrusions that are metasomatized and exhibit Ni‐Cu‐PGE sulphide mineralization. To better constrain the role of metasomatism in the ore genesis, we studied the best‐preserved pipe at Valmaggia which was emplaced 249 Myrs ago. Phlogopite 40 Ar/ 39 Ar analyses show that the pipe was infiltrated by metasomatic fluids derived from the subcontinental lithospheric mantle (SCLM) in two pulses at ~208 Ma and ~189 Ma which introduced sulphides into the pipe. Consequently, the pipe repeatedly acted as a preferred path for mass transfer from the SCLM into the lower crust over >60 Myrs (i.e., emplacement to second metasomatic pulse). Uplifted block margins, such as the Ivrea‐Verbano Zone, are potentially important exploration targets for magmatic sulphides. We argue that exploration strategies should focus on structures such as pipes that can focus metasomatic agents during ascent through the lithosphere.