Luciano Ungaretti

Bio: Luciano Ungaretti is an academic researcher from University of Pavia. The author has contributed to research in topics: Crystal structure & Staurolite. The author has an hindex of 23, co-authored 48 publications receiving 4870 citations.

Nomenclature of amphiboles Report of the Subcommittee on Amphiboles of the International Mineralogical Association Commission on New Minerals and Mineral Names;Nomenclature of amphiboles Report of the Subcommittee on Amphiboles of the International Mineralogical Association Commission on New Minerals and Mineral Names

Abstract: The International Mineralogical Association's approved amphibole nomenclature has been revised to simplify it, make it more consistent with divisions generally at 50%, define prefixes and modifiers more precisely, and include new amphibole species discovered and named since 1978, when the previous scheme was approved. The same reference axes form the basis of the new scheme and most names are little changed, but compound species names like tremolitic hornblende (now magnesiohornblende) are abolished, as are crossite (now glaucophane or ferroglaucophane or magnesioriebeckite or riebeckite), tirodite (now manganocummingtonite), and dannemorite (now manganogrunerite). The 50% rule has been broken only to retain tremolite and actinolite as in the 1978 scheme; the sodic-calcic amphibole range has therefore been expanded. Alkali amphiboles are now sodic amphiboles. The use of hyphens is defined. New amphibole names approved since 1978 include nyboite, leakeite, kornite, ungarettiite, sadanagaite, and cannilloite. All abandoned names are listed. The formulae and source of the amphibole end-member names are listed and procedures outlined to calculate Fe (super 3+) and Fe (super 2+) where not determined by analysis.

The behaviour of Ti in amphiboles; I, Four- and six-coordinate Ti in richterite

Abstract: The crystal structures and site-populations of 12 richterites have been refined to R indices of 1-2% using single-crystal MoKα X-ray diffraction data. Potassium-fluor-richterites from lamproites are characterized by [4] (Si+Al) sums less than 8.0 apfu (atoms per formula unit), suggesting the presence of other isomorphous tetrahedral substituents; richterites from other environments do not show this feature. The results of the structure refinements (mean bond lengths and mean atomic numbers) and crystal-chemical arguments show [4] i 4+ to occur at the t52) site in lamproitic richterites. Some richterites also show significant amounts of Ti 4+ in octahedral coordination; combination of site occupancy refinement and stereochemical data show [6] Ti 4+ to occur almost entirely at the M(1) site in these amphiboles, locally associated with the occurrence of O 2− at the adjacent O(3) site(s)

Crystal-chemistry and cation ordering in the system diopside-jadeite: A detailed study by crystal structure refinement

Abstract: The Nybo eclogite pod in Norway is characterized by a great variety of clinopyroxene compositions with Jd contents ranging from less than 5% up to nearly 80%, whilst Ac+Hd contents remain almost constant (mostly within 10±5%). Unconstrained X-ray structure refinement has been carried out on 16 pyroxene crystals (8 with C2/c and 8 with P2/n space group) from the Nybo eclogite, and also on one omphacite crystal (from Lago Mucrone in the Sesia-Lanzo Zone, Western Alps) which displays the highest degree of cation ordering yet described. The final discrepancy factors range from 0.014 to 0.029. The population of the sites has been determined on the basis of bond length considerations and of the results of the site occupancy refinement. Six of these crystals were subsequently analysed by electron microprobe. The tetrahedral sites are occupied by Si with negligible amounts of Al. Al, Mg, Fe3+ and Fe2+ occur at the octahedral sites; in the ordered P2/n crystals Al and Fe3+ are concentrated at the M11 site, whilst Mg and Fe2+ are concentrated and the M1 site. The eight-coordinated sites contain Ca and Na with negligible amounts of Fe and/or Mg. Ordering of Ca and Na takes place in the P2/n samples in such a way that in the most ordered crystal the M2 site contains almost exactly 0.75 Na+0.25 Ca and the M21 site 0.25 Na+0.75 Ca. Some geometrical features of the tetrahedra as well as of the octahedra (e.g. tetrahedral quadratic elongation and TILT angle) are not a simple linear function of composition, even when no change in space group occurs. The crystals evidently do not behave like a binary system of the two components, Di and Jd, but behave rather as if the composition Di0.50 Jd0.50 was a distinct end member. The boundaries between disordered and ordered phases in the Nybo pyroxenes fall at about 0.35 and 0.65 Jd/(Di+ Jd), in close agreement with the previous TEM investigations. The degree of order varies with composition following a bell-shaped curve: different coaxial bell-shaped curves can be drawn for crystals which have similar compositions but come from different metamorphic environments. The order vs composition diagrams may be useful for the interpretation of the P-T-t histories of the host rocks.

An internally consistent thermodynamic data set for phases of petrological interest

Abstract: The thermodynamic properties of 154 mineral end-members, 13 silicate liquid end-members and 22 aqueous fluid species are presented in a revised and updated data set. The use of a temperature-dependent thermal expansion and bulk modulus, and the use of high-pressure equations of state for solids and fluids, allows calculation of mineral–fluid equilibria to 100 kbar pressure or higher. A pressure-dependent Landau model for order–disorder permits extension of disordering transitions to high pressures, and, in particular, allows the alpha–beta quartz transition to be handled more satisfactorily. Several melt end-members have been included to enable calculation of simple phase equilibria and as a first stage in developing melt mixing models in NCKFMASH. The simple aqueous species density model has been extended to enable speciation calculations and mineral solubility determination involving minerals and aqueous species at high temperatures and pressures. The data set has also been improved by incorporation of many new phase equilibrium constraints, calorimetric studies and new measurements of molar volume, thermal expansion and compressibility. This has led to a significant improvement in the level of agreement with the available experimental phase equilibria, and to greater flexibility in calculation of complex mineral equilibria. It is also shown that there is very good agreement between the data set and the most recent available calorimetric data.

Nomenclature of amphiboles Report of the Subcommittee on Amphiboles of the International Mineralogical Association Commission on New Minerals and Mineral Names;Nomenclature of amphiboles Report of the Subcommittee on Amphiboles of the International Mineralogical Association Commission on New Minerals and Mineral Names

Abstract: The International Mineralogical Association's approved amphibole nomenclature has been revised to simplify it, make it more consistent with divisions generally at 50%, define prefixes and modifiers more precisely, and include new amphibole species discovered and named since 1978, when the previous scheme was approved. The same reference axes form the basis of the new scheme and most names are little changed, but compound species names like tremolitic hornblende (now magnesiohornblende) are abolished, as are crossite (now glaucophane or ferroglaucophane or magnesioriebeckite or riebeckite), tirodite (now manganocummingtonite), and dannemorite (now manganogrunerite). The 50% rule has been broken only to retain tremolite and actinolite as in the 1978 scheme; the sodic-calcic amphibole range has therefore been expanded. Alkali amphiboles are now sodic amphiboles. The use of hyphens is defined. New amphibole names approved since 1978 include nyboite, leakeite, kornite, ungarettiite, sadanagaite, and cannilloite. All abandoned names are listed. The formulae and source of the amphibole end-member names are listed and procedures outlined to calculate Fe (super 3+) and Fe (super 2+) where not determined by analysis.

Nomenclature of amphiboles; report of the subcommittee on amphiboles of the International Mineralogical Association, Commission on New Minerals and Mineral Names

Abstract: The International Mineralogical Association's approved amphibole nomenclature has been revised to simplify it, make it more consistent with divisions generally at 50%, define prefixes and modifiers more precisely, and include new amphibole species discovered and named since 1978, when the previous scheme was approved. The same reference axes form the basis of the new scheme and most names are little changed, but compound species names like tremolitic hornblende (now magnesiohornblende) are abolished, as are crossite (now glaucophane or ferroglaucophane or magnesioriebeckite or riebeckite), tirodite (now manganocummingtonite), and dannemorite (now manganogrunerite). The 50% rule has been broken only to retain tremolite and actinolite as in the 1978 scheme; the sodic-calcic amphibole range has therefore been expanded. Alkali amphiboles are now sodic amphiboles. The use of hyphens is defined. New amphibole names approved since 1978 include nyboite, leakeite, kornite, ungarettiite, sadanagaite, and cannilloite. All abandoned names are listed. The formulae and source of the amphibole end-member names are listed and procedures outlined to calculate Fe (super 3+) and Fe (super 2+) where not determined by analysis.

Non-ideal interactions in calcic amphiboles and their bearing on amphibole-plagioclase thermometry

Abstract: Amphibole thermodynamics are approximated with the symmetric formalism (regular solution model for within-site non-ideality and a reciprocal solution model for cross-site-terms) in order to formulate improved thermometers for amphibole-plagioclase assemblages. This approximation provides a convenient framework with which to account for composition-dependence of the ideal (mixing-on-sites) equilibrium constants for the equilibria: For A and B all possible within-site and cross-site interactions among the species □−K−Na−Ca−Mg−Fe2+−Fe3+−Al−Si on the A, M4, M1, M3, M2 and T1 amphibole crystallographic sites were examined. Of the 36 possible interaction energy terms, application of the symmetric formalism results in a dramatic simplification to eight independent parameters. Plagioclase nonideality is modelled using Darken's quadratic formalism. We have supplemented an experimental data set of 92 amphibole-plagioclase pairs with 215 natural pairs from igneous and metamorphic rocks in which the pressure and temperature of equilibration are well constrained. Regression of the combined dataset yields values for the eight interaction parameters as well as for apparent enthalpy, entropy and volume changes for each reaction. These parameters are used to formulate two new thermometers, which perform well (±40°C) in the range 400–1000°C and 1–15 kbar over a broad range of bulk compositions, including tschermakitic amphiboles from garnet amphibolites which caused problems for the simple thermometer of Blundy and Holland (1990). For silica-saturated rocks both thermometers may be applied: in silica-undersaturated rocks or magmas thermometer B alone can be applied. An improved procedure for estimation of ferric iron in calcic amphiboles is presented in the appendix.