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The Sheahan Diamond Literature Reference Compilation - Technical, Media and Corporate Articles based on Major Region - Italy
The Sheahan Diamond Literature Reference Compilation is compiled by Patricia Sheahan who publishes on a monthly basis a list of new scientific articles related to diamonds as well as media coverage and corporate announcements called the Sheahan Diamond Literature Service that is distributed as a free pdf to a list of followers. Pat has kindly agreed to allow her work to be made available as an online digital resource at Kaiser Research Online so that a broader community interested in diamonds and related geology can benefit. The references are for personal use information purposes only; when available a link is provided to an online location where the full article can be accessed or purchased directly. Reproduction of this compilation in part or in whole without permission from the Sheahan Diamond Literature Service is strictly prohibited. Return to Diamond Region Index
Sheahan Diamond Literature Reference Compilation - Scientific Articles by Author for all years
Each article reference in the SDLRC is tagged with one or more key words assigned by Pat Sheahan to highlight the main topics of the article. In addition most references have been tagged with one or more region words. In an effort to make it easier for users to track down articles related to a specific region, KRO has extracted these region words and developed a list of major region words presented in the Major Region Index to which individual region words used in the article reference have been assigned. Each individual Region Report contains in chronological order all the references with a region word associated with the Major Region word. Depending on the total for each reference type - technical, media and corporate - the references will be either in their own technical, media or corporate Region Report, or combined in a single report. Where there is a significant number of technical references there will be a technical report dedicated to the technical articles while the media and corporate references are combined in a separate region report. References that were added in the most recent monthly update are highlighted in yellow within the Region Report. The Major Region words have been defined by a scale system of "general", "continent", "country", "state or province" and "regional". Major Region words at the smaller scales have been created only when there are enough references to make isolating them worthwhile. References not tagged with a Region are excluded, and articles with a region word not matched with a Major Region show up in the "Unknown" report.
Kimberlite - diamondiferous
Lamproite - diamondiferous
Lamprophyre - diamondiferous
Other - diamondiferous
Kimberlite - non diamondiferous
Lamproite - non diamondiferous
Lamprophyre - non diamondiferous
Other - non diamondiferous
Kimberlite - unknown
Lamproite - unknown
Lamprophyre - unknown
Other - unknown
Future Mine
Current Mine
Former Mine
Click on icon for details about each occurrence. Works best with Google Chrome.
CITATION: Faure, S, 2010, World Kimberlites CONSOREM Database (Version 3), Consortium de Recherche en Exploration Minérale CONSOREM, Université du Québec à Montréal, Numerical Database on consorem.ca. NOTE: This publicly available database results of a compilation of other public databases, scientific and governmental publications and maps, and various data from exploration companies reports or Web sites, If you notice errors, have additional kimberlite localizations that should be included in this database, or have any comments and suggestions, please contact the author specifying the ID of the kimberlite: [email protected]
Minette inclusions in the rhyodacitic lavas of Mt. Amiata(CentralItaly); mineralogical and chemical evidence of mixing between Tuscan and Roman type lavas
Journal of Vol. Geotherm. Research, Vol. 19, No. 1-2, pp. 1-35
Potassic volcanism working group post congress excursion -volcanism in the Umbria-latium ultra alkaline district, Italy
International Conference on active volcanoes and risk mitigation, Field trip Sept. 2-, Department Scienze Della Terra, Piazza University of 06100 Perugia
Zirconolite and Zr Th U minerals in chromities of the Finero complex, western Alps, Italy: evidence for carbonatite type metasomatism in a subcontinental ... mantle plume.
Variable temperature 27Al and 29Si NMR studies of synthetic forsterite and Fe bearing Dora Maira pyrope garnet: temperature dependence and mechanisms of paramagnetically shifted peaks.
Earth and Planetary Science Letters, Vol. 447, pp. 151-160.
Mantle, Europe, Italy
Kimberlite formation, volcanism, melting
Abstract: Kimberlites are the most deep-seated magmas in the mantle and ascend to the surface at an impressive speed, travelling hundreds of kilometres in just hours while carrying a substantial load of xenolithic material, including diamonds. The ascent dynamics of these melts are buoyancy-controlled and certainly driven by outgassing of volatile species, presumably H2O and CO2, summing to concentration level of ca 15 -30 wt.% in kimberlite melts. We provide H2O -CO2 solubility data obtained on quenched glasses that are synthetic analogues of kimberlite melts (SiO2 content ranging from 18 to 28 wt.%). The experiments were conducted in the pressure range 100 to 350 MPa. While the CO2 solubility can reach 20 wt.%, we show that the H2O solubility in these low silica melts is indistinguishable from that found for basalts. Moreover, whereas in typical basalts most of the water exsolves at shallower pressure than the CO2, the opposite relationship is true for the low-SiO2 composition investigated. These data show that kimberlites can rise to depths of the upper crust without suffering significant degassing and must release large quantities of volatiles (>15 wt.%) within the very last few kilometres of ascent. This unconventional degassing path may explain the characteristic pipe, widening-upward from a ?2.5 km deep root zone, where kimberlites are mined for diamonds. Furthermore, we show that small changes in melt chemistry and original volatile composition (H2O vs. CO2) provide a single mechanism to explain the variety of morphologies of kimberlite pipes found over the world. The cooling associated to such massive degassing must freeze a large quantity of melt explaining the occurrence of hypabyssal kimberlite. Finally, we provide strong constraints on the primary volatile content of kimberlite, showing that the water content reported for kimberlite magma is mostly reflective of secondary alteration.
Abstract: This paper is an updated overview, including many new data, of what is known about Italian alkaline-carbonatite complexes, plus a new description of a carbothermal residua-related district, and its potential for mineral deposits. The Italian carbonatite occurrences can be divided into two belts. The first is a 350 km long and 75 km wide belt along the Apennines mountain range mainly with primary extrusive carbonatites generally from monogenic volcanoes and from the Vulture volcanic complex; the second belt is 60 km long and 20 km wide in the Northern Latium region in which carbothermal residua carbonatites and fluorite mineralisation deposited by high-temperature fluids rich in CO2, SO2 and fluorine are occurring in caldera volcanoes. Several of the raw materials, such as Light Rare Earth Elements, vanadium, niobium, zirconium, fluorite and phosphate are identified as critical as well as other commodities, occur in Italian carbonatites and alkaline rocks. At the Pianciano quarry (Bracciano) fluorite-rich ore (fluor-ore = fluorite in a mineralised gangue) is actually exploited as flux for cement, but Rare Earth Elements (+ V) could be a notable by-product (300,000 metric tonnes, equivalent to 4.2% of European resources). Pyrochlore, monazite, apatite, and britholite bearing subvolcanic rocks in ejecta from the Vulture volcano are of a near-economic grade, but their geological constraints are not known. A conceptual framework of combined geological and geochemical data improves the general understanding of this regional magmatic system, aimed at laying the foundations of a future geological model disclosing unrecognised potential exploration targets. However, this paper is not intended for direct use by the exploration industry; rather it is principally aimed at mineralogists and petrologists who could develop strategies for the identification of unexposed or unrecognised deposits.
Abstract: Micas from mafic ultrapotassic rocks with lamproitic affinity from several localities of the Central Mediterranean region were studied through single-crystal X-ray diffraction (SC-XRD), electron microprobe analysis (EMPA) and Secondary Ion Mass Spectrometry (SIMS); Mössbauer Spectroscopy (MöS), when feasible, was also applied to minimise the number of unknown variables and uncertainties. Lamproitic samples analysed cover the most important Central Mediterranean type localities, from Plan d'Albard (Western Alps) to Sisco (Corsica), Montecatini Val di Cecina and Orciatico (Tuscany, Italy) and Torre Alfina (Northern Latium, Italy). The studied crystals show distinctive chemical and structural features; all of them belong to the phlogopite-annite join and crystallise in the 1 M polytype, except for micas from Torre Alfina, where both 1 M and 2 M1 polytypes were found. Studied micas have variable but generally high F and Ti contents, with Mg/(Mg + Fe) ranging from ~ 0.5 to ~ 0.9; 2M1 crystals from Torre Alfina radically differ in chemical composition, showing high contents of Ti and Fe as well as of Al in both tetrahedra and octahedra, leading to distinctive structural distortions, especially in tetrahedral sites. SIMS data indicate that studied micas are generally dehydrogenated with OH contents ranging from ~ 0.2 apfu (atoms per formula unit) for Orciatico and Torre Alfina to ~ 1.4 for Plan d'Albard crystals; this feature is also testified by the length of the c parameter, which decreases with the loss of hydrogen and/or the increase of the F ? OH substitution. Chemical and structural data suggest that the entry of high charge octahedral cations is mainly balanced by an oxy mechanism and, to a lesser extent, by a M3 +,4 +-Tschermak substitution. Our data confirm that Ti preferentially partitions into the M2 site and that different Ti and F contents, as well as different K/Al values, are both dependant upon fH2O and the composition of magma rather than controlled by P and T crystallisation conditions. The obtained data help to discriminate among lamproite-like rocks formed within a complex geodynamic framework but still related to a destructive tectonic margin and evidence different trends for micas from the youngest Torre Alfina (Northern Latium) lamproites, referred to the Apennine orogeny and those of the older lamproites from Orciatico, Montecatini Val di Cecina (Tuscany), Western Alps, and Corsica, the latter referred to the Alpine orogeny. Phlogopite crystals from the older lamproites fall within the compositional and structural field of worldwide phlogopites from both within-plate and subduction-related settings. Phlogopite from the Plio-Pleistocene lamproite-like occurrence in Tuscany and Northern Latium, despite crystals with low Mg# of the Torre Alfina rock plot well within the general field of the other crystals in less evolved samples, follows a different evolution trend similar to that of shoshonites from Tuscany and Northern Latium. On this basis, we argue that the observed differences are inherited by slight differences in the magma compositions that are related with different genetic and evolution pathways.
Geochimica et Cosmochimica Acta, Vol. 233, pp. 95-114.
Europe, Italy
shoshonites
Abstract: The diffusive exchange of 30 trace elements (Cs, Rb, Ba, Sr, Co, Y, La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, Lu, Ta, V, Cr, Pb, Th, U, Zr, Hf, Sn and Nb) during the interaction of natural mafic and silicic alkaline melts was experimentally studied at conditions relevant to shallow magmatic systems. In detail, a set of 12 diffusion couple experiments have been performed between natural shoshonitic and rhyolitic melts from the Vulcano Island (Aeolian archipelago, Italy) at a temperature of 1200?°C, pressures from 50 to 500?MPa, and water contents ranging from nominally dry to ca. 2 wt.%. Concentration-distance profiles, measured by Laser Ablation ICP-MS, highlight different behaviours, and trace elements were divided into two groups: (1) elements with normal diffusion profiles (13 elements, mainly low field strength and transition elements), and (2) elements showing uphill diffusion (17 elements including Y, Zr, Nb, Pb and rare earth elements, except Eu). For the elements showing normal diffusion profiles, chemical diffusion coefficients were estimated using a concentration-dependent evaluation method, and values are given at four intermediate compositions (SiO2 equal to 58, 62, 66 and 70 wt.%, respectively). A general coupling of diffusion coefficients to silica diffusivity is observed, and variations in systematics are observed between mafic and silicic compositions. Results show that water plays a decisive role on diffusive rates in the studied conditions, producing an enhancement between 0.4 and 0.7 log units per 1 wt.% of added H2O. Particularly notable is the behaviour of the trivalent-only REEs (La to Nd and Gd to Lu), with strong uphill diffusion minima, diminishing from light to heavy REEs. Modelling of REE profiles by a modified effective binary diffusion model indicates that activity gradients induced by the SiO2 concentration contrast are responsible for their development, inducing a transient partitioning of REEs towards the shoshonitic melt. These results indicate that diffusive fractionation of trace elements is possible during magma mixing events, especially in the more silicic melts, and that the presence of water in such events can lead to enhanced chemical diffusive mixing efficiency, affecting also the estimation of mixing to eruption timescales.
Diamond & Related Materials, Vol. 90, pp. 188-193.
Europe, Italy
diamond radiation
Abstract: During the last decades many studies have been carried out to investigate how point defects and aggregates respond and evolve in natural Type Ia diamonds as a result of treatments, and a number of underlying mechanisms have been identified and interpreted. However, the analysis of radiation-induced creation/ionization of defects, as well as their migration and aggregation in secondary defect structures, often requires experimental approaches which can hardly constitute a simple-to-use diagnostic tool for the identification of artificially treated diamonds. Here we disclose a novel simple indicator of artificial exposure of Type Ia diamonds to ionizing radiations and subsequent annealing. This indicator consists in narrow photoluminescence lines in the red region, between 681 and 725?nm, we recently found to result from vacancies trapped by interstitial carbon aggregates and platelets. Our results demonstrate that interstitial structures become sites of vacancy trapping - by thermal migration of radiation-induced vacancies - only when diamond undergoes treatments. We give the rigorous validation of the new spectroscopic probe of artificial treatments analysing photoluminescence and infrared absorption spectra of well-known H1b and H1c centres in a hundred samples. Importantly, the method is based on emission lines which do not require neither high photon-energy excitation nor cryogenic temperatures.
Nature Communications, doi.org/10.1038/ s41467-019-11072-5 10p. Pdf
Europe, Italy
subduction
Abstract: Recycling of Earth’s crust through subduction and delamination contributes to mantle heterogeneity. Melt inclusions in early crystallised magmatic minerals record greater geochemical variability than host lavas and more fully reflect the heterogeneity of magma sources. To date, use of multiple isotope systems on small (
Abstract: The Mt. Vulture (Basilicata, Southern Italy) is an alkaline carbonatite volcano whose extrusive rocks are mafic, alkaline with different Na/K ratios, mainly SiO2 undersaturated, with relatively high contents of Cl, S, F, and CO2 [1]. Their composition ranges from basalts to basanites to tephrite to phono-tephrites and phonolites. Along with this magma suite have been erupted mantle xenolith bearing-carbonatitic melilitites and carbonatites [1, 2]. Holocrystalline ejecta have been studied in detail to reconstruct the composition of the subvolcanic/plutonic bodies beneath Mt. Vulture. The ejacta are haüine-bearing clinopyoxenites with variable content of olivine, amphibole and phlogopite, haüine foidolites with some nepheline and leucite, haüine-calcite-syenites, syenites, calcite melilitolites, K-feldspar bering-alvikites and a sovite [3]. There is a continuous variation in the modal and geochemical composition between clinopyroxenite and foidolite, that might be related to the chemical evolution shown by the extrusive rocks. The ejecta show an enrichment trend in LILE, LREE and HFSE consistent with fractional crystallisation evolution, from clinopyroxenites to foidolites and from foid-syenites to syenites. The foid-syeniites are rich in U, Pb, Sr, LREE and contain britholite, wholerite, Upyrochlore. The most evolved syenite however, is less enriched in REE but contains elevate content of U and HFSE. The sovite contains intercumulus alkali carbonates. A glimemerite vein in a haüine foidolite contain REE-rich apatite, shorlomite and U-pyrochlore. These findings suggest that alkaline-alogen-H2O-CO2 rich fluids can be formed during sub-volcanic/plutonic fractional crystallisation. These fluids can produce fenitisation and/or can form mineralisation enriched in REE and HFSE. The ejecta suite studied represents the intrusive complex beneath the volcano and these rock types are typical of ring complexes in alkaline carbonatite volcanoes.
Abstract: A new discovery of carbonatites at Pianciano, Ficoreto and Forcinelle in the Roman Region demonstrates that Italian carbonatites are not just isolated, mantle xenoliths-bearing, primitive diatremic rocks but also evolved sub-type fluor-calciocarbonatite (F?10 wt.%) associated with fluor ore (F?30 wt.%). New data constrain a multi-stage petrogenetic process, 1-orthomagmatic, 2-carbothermal, 3-hydrothermal. Petrography and geochemistry are conducive to processes of immiscibility and decarbonation, rather than assimilation and crystal fractionation. A CO2-rich, ultra-alkaline magma is inferred to produce immiscible melilite leucitite and carbonatite melts, at lithospheric mantle depths. At the crustal level and in the presence of massive CO2 exsolution, decarbonation reactions may be the dominant processes. Decarbonation consumes dolomite and produces calcite and periclase, which, in turn, react with silica to produce forsterite and Ca silicates (monticellite, melilite, andradite). Under carbothermal conditions, carbonate breakdown releases Sr, Ba and LREE; F and S become concentrated in residual fluids, allowing precipitation of fluorite and barite, as well as celestine and anhydrite. Fluor-calciocarbonatite is the best candidate to exsolve fluids able to deposit fluor ore, which has a smaller volume. At the hydrothermal stage, REE concentration and temperature dropping allow the formation of LREEF2+ and LREECO3+ ligands, which control the precipitation of interstitial LREE fluorcarbonate and silicates -(bastnäsite-(Ce)- Ce(CO3)F and -britholite-(Ce)- (Ce,Ca)5(SiO4,PO4)3(OH,F) . Vanadates such as wakefieldite, CeVO4, vanadinite, Pb5(VO4)3Cl and coronadite Pb(Mn4+6 Mn3+2)O16 characterise the matrix. At temperatures of ?100°C analcime, halloysite, quartz, barren calcite, and zeolites (K-Ca) precipitate in expansion fractures, veins and dyke aureoles.
Abstract: A new discovery of carbonatites at Pianciano, Ficoreto and Forcinelle in the Roman Region demonstrates that Italian carbonatites are not just isolated, mantle xenoliths-bearing, primitive diatremic rocks but also evolved sub-type fluor-calciocarbonatite (F~10 wt.%) associated with fluor ore (F~30 wt.%). New data constrain a multi-stage petrogenetic process, 1-orthomagmatic, 2-carbothermal, 3-hydrothermal. Petrography and geochemistry are conducive to processes of immiscibility and decarbonation, rather than assimilation and crystal fractionation. A CO2-rich, ultra-alkaline magma is inferred to produce immiscible melilite leucitite and carbonatite melts, at lithospheric mantle depths. At the crustal level and in the presence of massive CO2 exsolution, decarbonation reactions may be the dominant processes. Decarbonation consumes dolomite and produces calcite and periclase, which, in turn, react with silica to produce forsterite and Ca silicates (monticellite, melilite, andradite). Under carbothermal conditions, carbonate breakdown releases Sr, Ba and LREE; F and S become concentrated in residual fluids, allowing precipitation of fluorite and barite, as well as celestine and anhydrite. Fluor-calciocarbonatite is the best candidate to exsolve fluids able to deposit fluor ore, which has a smaller volume. At the hydrothermal stage, REE concentration and temperature dropping allow the formation of LREEF2+ and LREECO3+ ligands, which control the precipitation of interstitial LREE fluorcarbonate and silicates -(bastnäsite-(Ce)- Ce(CO3)F and -britholite-(Ce)- (Ce,Ca)5(SiO4,PO4)3(OH,F) . Vanadates such as wakefieldite, CeVO4, vanadinite, Pb5(VO4)3Cl and coronadite Pb(Mn4+6 Mn3+2)O16 characterise the matrix. At temperatures of =100°C analcime, halloysite, quartz, barren calcite, and zeolites (K-Ca) precipitate in expansion fractures, veins and dyke aureoles.
Abstract: Naturalistic and geo?mineralogical museum collections are one of the most relevant sources for research on meteorites the world over. Here, we present the description of a new Italian meteorite that has been recently discovered at the Royal Mineralogical Museum of Naples in Italy.
Earth and Planetary Science Letters, Vol. 558, 115763, 6p. Pdf
Europe, Italy
UHP
Abstract: The stabilization of coesite is a diagnostic indicator of ultrahigh-pressure metamorphism and in many cases it implies that a rock has been subducted to a minimum depth of 80 km. Coesite typically occurs as rare relicts in rigid host minerals, but most commonly transforms into ?-quartz pseudomorphs during exhumation. The abundance of coesite-bearing rocks in orogens worldwide is a contentious issue in the petrological community, despite evidence from numerical modeling that suggests that coesite formation should be a common geological process during ultrahigh-pressure metamorphism. This knowledge gap must be addressed to improve the understanding of the geological aspects of subduction-zone geodynamics. Here we report that minuscule coesites (<20 ?m) occur as abundant inclusions in garnet-rich layers from the Italian Western Alps. The discovery of such intact inclusions may fill the gaps in the predicted and observed abundances of coesite worldwide. Through integrated approaches with resolutions down to the nano-scale, we show that these garnet-hosted inclusions are composed entirely of coesite. Our results suggest that common coesite-derived quartz pseudomorphs are less typical structures in ultrahigh-pressure metamorphic rocks and the minuscule coesite in many rocks may be overlooked because of its size. These findings open up new research directions for constraining the extent of deeply subducted rocks and their rheology.
Geological Society, London Special Publication, doi.org/10.1144/SP513-2021-36 49p. Pdf
Europe, Italy, France, Spain, Serbia, Macedonia, Turkey
lamproites
Abstract: High-MgO lamproite and lamproite-like (i.e., lamprophyric) ultrapotassic rocks are recurrent in the Mediterranean and surrounding regions. They are associated in space and time with ultrapotassic shoshonites and high-K calc-alkaline rocks. This magmatism is linked with the geodynamic evolution of the westernmost sector of the Alpine-Himalaya collisional margin, which followed the closure of the Tethys ocean. Subduction-related lamproites, lamprophyres, shoshonites and high-K calc-alkaline suites were emplaced in the Mediterranean region in the form of shallow level intrusions (e.g., plugs, dykes, and laccoliths), and small volume lava flows, with very subordinate pyroclastic rocks, starting from the Oligocene, in the Western Alps (Northern Italy), through the Late Miocene in Corsica (Southern France) and in Murcia-Almeria (South-Eastern Spain), to the Plio-Pleistocene in Southern Tuscany and Northern Latium (Central Italy), in the Balkan peninsula (Serbia and Macedonia), and in the Western Anatolia (Turkey). The ultrapotassic rocks are mostly lamprophyric, but olivine latitic lavas with a clear lamproitic affinity are also found, as well as dacitic to trachytic differentiated products. Lamproite-like rocks range from slightly silica under-saturated to silica over-saturated composition, have relatively low Al2O3, CaO, and Na2O contents, resulting in plagioclase-free parageneses, and consist of abundant K-feldspar, phlogopite, diopsidic clinopyroxene and highly forsteritic olivine. Leucite is generally absent and it is rarely found only in the groudmasses of Spanish lamproites. Mediterranean lamproites and associated rocks share an extreme enrichment in many incompatible trace elements and depletion in High Field Strength Elements and high, and positively correlated Th/La and Sm/La ratios. They have radiogenic Sr and unradiogenic Nd isotope compositions, high 207Pb over 206Pb and high time integrated 232Th/238U. Their composition requires an originally depleted lithospheric mantle source metasomatised by at least two different agents: i) a high Th/La and Sm/La (i.e., SALATHO) component deriving from lawsonite-bearing, ancient crustal domains likely hosted in mélanges formed during the diachronous collision of the northward drifting continental slivers from Gondwana; ii) a K-rich component derived from a recent subduction and recycling of siliciclastic sediments. These metasomatic melts produced a lithospheric mantle source characterised by network of felsic and phlogopite-rich veins, respectively. Geothermal readjustment during post-collisional events induced progressive melting of the different types of veins and the surrounding peridotite generating the entire compositional spectrum of the observed magmas. In this complex scenario, orogenic Mediterranean lamproites represent rocks that characterise areas that were affected by multiple Wilson cycles, as observed in the the Alpine-Himalayan realm.
Geochimica et Cosmochimica Acta, Vol. 306, pp. 143-170. pdf
Europe, Italy
subduction
Abstract: The volatile transfer in subduction zones and the role of sulfate as a vector for the mobilization of oxidized components from down-going slabs remain hotly debated issues. Orogenic spinel and garnet peridotite lenses from the Ulten Zone (Eastern Alps, Italy), exhumed as part of felsic metamorphic terranes in continental collision zones, bear witness to mass transfer processes in these pivotal environments. In this study, we carried out a multi-method investigation of mantle sulfides coexisting with four generations of carbonates, indicating coupled sulfur and carbon mobility throughout the peridotites’ metamorphic evolution as part of the Variscan subduction architecture. Detailed petrography, bulk rock measurements, in situ chemical and geochemical analyses of sulfides as well as Sr isotope analyses of associated clinopyroxene and amphibole are combined with the aim to constrain the origin, nature and effect of multiple C-O-H-S-bearing fluids and melts the peridotites interacted with. The first, pre-peak, metasomatic pulse (Stage 1) is represented by an H2S-CO2-bearing melt from the subduction-modified hot mantle wedge, which formed a pyroxenite layer hosting matrix pentlandite with ?34S of +2.77‰. Matrix carbonates occasionally occur in the coarse-grained peridotite under eclogite-facies conditions (Stage 2), with heavier ?34S (up to +3.43‰), radiogenic Sr (87Sr/86Srclinopyroxene > 0.7052) and elevated Pb abundances. These are ascribed to interaction with isotopically heavy melts carrying recycled crustal component, permissive of, but not requiring, involvement of oxidized S species. Conversely, isotopically lighter matrix pentlandite (?34S = ?1.62 to +0.67‰), and radiogenic Sr in amphibole (87Sr/86Sr = 0.7056) and associated dolomite (published data) from fine-grained garnet-amphibole peridotites may point to involvement of H2S-CO2-bearing crustal fluids, which variably equilibrated with the mantle before interacting with the peridotites. The post-peak Stage 3 marks the entrapment of peridotites into a tectonic mélange. Here, kelyphitization of garnet is catalyzed by further ingress of a S-bearing fluid (?34S = ?0.38‰), while carbonate veining with occasional sulfides bear witness to channelized fluid flow. Sulfide and amphibole grains in retrogressed spinel peridotites reveal the highest contents of fluid-mobile elements (As, Sb) and 87Sr/86Sramphibole up to 0.7074, suggesting late interactions with isotopically heavy crustal fluids at high fluid-rock ratios. Textural observations indicate that, during Stage 4, serpentinization of peridotites at low ƒS2 played an active role not only in CO2 release by conversion of dolomite to calcite + brucite intergrowths, but also in local removal of 32S during the final exhumation stage. Late channelized sulfur remobilization is evidenced by the serpentine + magnetite (±millerite ± calcite) vein carrying > 300 ppm S. Overall, the relatively narrow range of sulfur isotope composition (?34S = ?1.62 to +3.76‰) is indicative of limited interaction with isotopically heavy crustal liquids, and points to a subordinate role of subduction-derived sulfate throughout the extended fluid(melt)/rock evolution of the Ulten Zone peridotites, first in the mantle wedge and then as part of a tectonic mélange.
Abstract: The goal of this work is to investigate the diamond collection preserved at the Natural History Museum of the University of Firenze (MSN-FI) using a multidisciplinary approach. The mixed methods combine historical research with spectroscopic techniques to gain a deeper understanding of this collection of great historical, scientific and gemmological interest. This study concerns the analysis of 61 diamonds that are relatively small in both size and weight, mostly unworked and sometimes rich in inclusions. These specimens were acquired by MSN-FI from diverse collectors and institutions from 1824 until the most recent acquisitions in the 1990s. The FTIR spectroscopy was performed on 45 specimens. The results show the physical classification of diamonds in three groups (IaAB, IaA, and IaB) and reveal the presence of hydrogen as ethylene -CH?=?CH- or vinylidene?>?C?=?CH2 group.
Abstract: During my doctoral studies, in the late 1980s, I realised that the Italian kamafugites (kalsilite melilitites) had to be related to carbonatite magmatism. I started a detailed study of the kamafugitic sites, and I explored remote areas deep in Italy’s Apennine mountains. When I found the Polino carbonatite, I put a few drops of acid on it, and the rock reacted. I have a vivid memory of my heart beating faster. I had found it! My fellow geologists were somewhat sceptical, but the late Professor Giorgio Marinelli (1922-1993) encouraged me and predicted many new carbonatite discoveries. He was right. Overcoming my Latin temperament, I focused on the concept that carbonatites, however unusual as rocks, cannot be dismissed as simple geological oddities but require detailed and comprehensive study. I am fond of all the history that marked my latest 40 years of life, and it reminds me of the many friends and mentors that I have had, especially when I was a young researcher. Sadly, some of them are no longer with us. I am so grateful to them, and I consider it a life-changing experience to have met them
