GLORIA

GEOMAR Library Ocean Research Information Access

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
  • 1
    Publication Date: 2021-01-14
    Description: We present elemental maps and intra-crystal compositional profiles conducted on a representative clinopyroxene phenocryst from the 1974 eccentric lava flows at Mt. Etna volcano (Sicily, Italy). The eruption was fed by deep-seated and primitive magmas ascending through pathways bypassing the central volcanic conduits. These magmas show MgO and Cr contents higher (and REE + Y lower) than those characterizing younger and more evolved eruptions, albeit the bulk rock compositions of both primitive and more evolved products are invariably classified as trachybasalts in the TAS (total alkali vs. silica) diagram. Mafic recharge episodes are recorded by the complex textural features of the clinopyroxene, with a subrounded core enclosed within a concentrically zoned mantle. The core is enriched in Mg + Fe2++Na and depleted in Fe3++Ca relative to the mantle. The jadeite (Jd) component decreases from core to mantle and is counterbalanced by higher Ca-Tschermak (CaTs) contents, as the number of TAl cations in tetrahedral coordination increases. The Jd-rich core incorporates high proportions of rare earth elements and Y (REE + Y) and low concentrations of high field strength elements (HFSE) and transition elements (TE, such as Ni, Cr and Sc), whereas the opposite occurs for the CaTs-rich mantle. The decoupling of REE + Y and HFSE argues against simple changes in melt composition and indicates an additional mechanism driving trace element zonations. Thermobarometric calculations indicate that the early-formed Jd-rich core equilibrated with the host magma at mantle depths (750–950 MPa and 1190–1210 °C), whereas the later CaTs-rich mantle formed at shallower crustal levels (400–700 MPa and 1150–1180 °C) after magma recharge. Quantitative modeling of apparent cation partitioning between clinopyroxene and melt (Di) indicates that DHFSE increase from the Jd-rich core to the CaTs-rich mantle. In contrast, DREE+Y increase up to one order of magnitude at the Jd-rich core due to the enhanced stability of an Na0.5REE + Y0.5MgSiO6 end-member. We infer that compositional changes in clinopyroxene due to the different P-T conditions of the plumbing system may control the concentrations of REE + Y in residual melts derived after partial crystallization and differentiation of primitive magmas, such as those feeding the 1974 eccentric eruption. On this basis, we use DREE+Y measured across the core-mantle interface to constrain the geochemical evolution of recent 2000–2013 magmas at Mt. Etna volcano by Rayleigh fractional crystallization. Results indicate that magma dynamics proceed via a stepwise polybaric-polythermal process accounting for 1) crystallization of Jd-rich clinopyroxenes at high-P, high-T conditions, 2) upward migration of crystal-bearing magmas due to replenishment phenomena with input of fresh magmas and 3) crystallization of CaTs-rich clinopyroxene in low-P, low-T reservoirs. The resulting total amount (~40 vol%) of clinopyroxene fractionated agrees with geophysical data suggesting the presence of highly crystalline magmatic bodies at shallow to intermediate crustal levels below Mt. Etna.
    Description: Published
    Description: 105382
    Description: 3V. Proprietà chimico-fisiche dei magmi e dei prodotti vulcanici
    Description: JCR Journal
    Repository Name: Istituto Nazionale di Geofisica e Vulcanologia (INGV)
    Type: article
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 2
    Publication Date: 2020-02-06
    Description: The magmatic architecture and physicochemical processes inside volcanoes influence the style and timescale of eruptions. A long-standing challenge in volcanology is to establish the rates and depths of magma storage and the events that trigger eruption. Magma feeder systems are remarkably crystal-rich, and the growth stratigraphy of minerals sampled by erupted magmas can reveal a wealth of information on pre-eruptive processes. Here we combine detailed textural and chemical data acquired on large (〉5 mm), euhedral augite megacrysts from Roman era activity (Pizzo scoria cone, 2.4–1.8 ka) at Stromboli (Italy) to investigate the plumbing system prior to the onset of current steady-state activity. Our dataset includes novel laser ablation time-of-flight mass spectrometry (LA-ICP-TOFMS) maps, which rapidly visualise multi-element zoning patterns across entire megacryst sections. The clinopyroxene data are complemented with geochemical constraints on mineral and melt inclusions, and adhering glassy tephra. Megacrysts are sector and oscillatory zoned in trace elements, yet their major element compositions are relatively uniform and in equilibrium with shoshonite-buffered melts. Mild sector zoning documents dynamic crystallisation under conditions of low undercooling during magma residence and growth. Clinopyroxene-melt thermobarometric and hygrometric calibrations, integrated with thermodynamically derived equilibrium equations, accurately track the P-T-H2O path of magmas. The refined models return restricted crystallisation depths that are deeper than those reported previously for historical and current eruptions, but consistent with deep clinopyroxene-dominated crystallisation (≥10 km), resembling other water-rich alkaline mafic systems. Megacryst cores are overgrown by oscillatory zoned mantles recording continuous input of magma that failed to trigger eruption. Crystal rims are characterised by a mild increase in compatible transition metals Cr and Ni, and depletion in incompatible elements, indicative of pre-eruptive mafic replenishment and magma mixing. The volcanic system appears to have been dominated by protracted periods of replenishment, convection, and crystal residence, punctuated by rapid megacryst evacuation and eruption upon arrival of more mafic magma (days-weeks). Since the inception of current steady-state activity, eruption-triggering melts have become appreciably more mafic, suggesting that intrusion of primitive magma may be a key driver of the steady-state regime.
    Description: Published
    Description: Article 239
    Description: 3V. Proprietà chimico-fisiche dei magmi e dei prodotti vulcanici
    Description: JCR Journal
    Repository Name: Istituto Nazionale di Geofisica e Vulcanologia (INGV)
    Type: article
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 3
    Publication Date: 2019-03-29
    Description: The 1669 eruption of Mt Etna was one of the most voluminous and devastating of its flank eruptions in historical times. Despite a large body of relevant research, knowledge of the timing and duration of magma transfer and magma recharge through the internal plumbing system preceding and during the eruption is still limited. To address that lack of knowledge, we apply a three-way integrated method, linking systems analysis of crystals, a time-integrated study of zoned olivine populations, and a forward-modelling approach using thermodynamic calculations. Analysis of 202 olivine crystals erupted during the initial (pre-March 20, i.e. SET1) and the final (post-March 20; i.e. SET2 and MtRs) stages of the eruption reveals the existence of three magmatic environments (MEs) in which the majority of the olivine cores [M1 (= Fo75–78)] and rims [i.e. M5 (= Fo51–59) and M3 (= Fo65–69)] formed. Application of the rhyolite-MELTS software allowed us to constrain the key intensive variables associated with these MEs. We find that temperature, water content and oxidation state vary between these MEs. Application of diffusion modelling to the zoned olivine crystals allowed us to reconstruct the timing and chronology of melt and crystal transfer prior to and during the 1669 flank eruption. We find that, following the formation of the olivine cores [M1 (= Fo75–78)], the reservoir M1 was intruded by batches of more evolved, degassed and possibly aphyric M5-type magma, commencing 1·5 years prior to eruptive activity. This is the origin of the SET1 olivine rims (i.e. Fo51–59). In the months prior to eruption, timescale data show that recharge activity along the newly established pathway M1–M5 increased notably. Starting in November 1668, only a few weeks after the first intrusive episode into the M1 reservoir, a second pulse of magma injections (M3-type magma) occurred and a new pathway M1–M3 opened; this is how the SET2 olivine rims (i.e. Fo65–69) formed. For several weeks a bifurcated transport system with two dominant magma pathways developed along M1–M5 and M1–M3 dyke injections. Accompanied by vigorous seismicity, in the days immediately before eruption the local magma transfer dynamics changed and the M1–M5 recharge activity slowed down, as shown by a relative lack of crystals recording shorter timescales. M1–M3 recharge, however, remained high and persisted following the eruption onset on March 11, during which the SET1 lavas were drained. We propose that the change of the local magma transfer dynamics might be linked to changes in the local stress field brought on during eruption. This may potentially have been due to repeated dyke injections into Etna’s shallow plumbing system disrupting the early M1–M5 pathway and at the same time stabilizing the M1–M3 route as a dominant feeder. This transfer of system feeding would reproduce the observed syn-eruptive recharge and mixing in the weeks following eruption onset, culminating in the eruption of the later SET2 lavas.
    Description: Published
    Description: 443–472
    Description: 1V. Storia eruttiva
    Description: 2V. Struttura e sistema di alimentazione dei vulcani
    Description: JCR Journal
    Repository Name: Istituto Nazionale di Geofisica e Vulcanologia (INGV)
    Type: article
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 4
    Publication Date: 2020-02-06
    Description: Isothermal and undercooling experiments were conducted on one of the most primitive trachybasalts from Mt. Etna volcano in order to examine the crystallization mechanisms controlling the textural and compositional variability of clinopyroxene. Experiments were performed at 400–800 MPa, 1050–1200 °C, 0–4 wt.% H2O and at oxygen fugacity 2 log units above the Ni-NiO + 2 buffer. In isothermal experiments, the final resting temperature is approached from room temperature and clinopyroxene growth is dominated by an interface-controlled mechanism, leading to the formation of small (∼10 µm) and euhedral crystals with homogeneous compositions. Conversely, in undercooling experiments, the final resting temperature is approached after annealing at temperature above the liquidus, imposing an effective degree undercooling (ΔT) to the system. In presence of undercooling, the crystallization of clinopyroxene is dominated by a diffusion-controlled mechanism that determines the formation of large (〉100 µm) crystals, constituted by two compositionally distinct domains, enriched in Al2O3 + TiO2 and SiO2 + MgO, respectively. The maximum growth rate (Gmax) decreases progressively from ∼10−7 to ∼10−8 cm/s as the degree of undercooling increases from ∼20 to ∼230 °C, due to the increase in nucleation rate. At low to moderate degrees of undercooling (ΔT = 23–41 °C) clinopyroxene is prevalently euhedral to subhedral, whereas at high degrees of undercooling, the crystal shape changes from prevalently subhedral (ΔT = 73–123 °C) to skeletal and dendritic (ΔT = 132–233 °C). Hourglass sector zoning similar to that documented for natural phenocrysts from eruptions at Mt. Etna volcano is observed only at low degrees of undercooling (ΔT = 23–32 °C). This type of zoning develops in the form of the cation exchange [Si + Mg]{-111} ↔ [Al + Ti]{100} and demonstrates that hourglass sector zoning is an effective indicator of sluggish kinetic effects caused by relatively low degrees of undercooling. In contrast, at increasing degrees of undercooling (ΔT 〉 32 °C), strong melt supersaturation determines the early formation of Al2O3 + TiO2-rich dendritic crystals and further SiO2 + MgO-rich overgrowths, as the bulk system attempts to return to a near-equilibrium state between the advancing crystal surface and the feeding melt. The experimentally-determined relationship between ΔT and clinopyroxene chemistry is used to reconstruct the crystallization conditions of natural clinopyroxenes from 1974 and 2002–2003 eccentric eruptions at Mt. Etna volcano. Clinopyroxene rims record much higher degrees of undercooling (up to ∼110 °C) than crystal mantles associated with magma recharge at depth (mostly 0–40 °C). Hence, the rims track decompression-induced degassing and cooling during the ascent of magma towards the surface.
    Description: Published
    Description: 258-276
    Description: 3V. Proprietà chimico-fisiche dei magmi e dei prodotti vulcanici
    Description: JCR Journal
    Repository Name: Istituto Nazionale di Geofisica e Vulcanologia (INGV)
    Type: article
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 5
    Publication Date: 2020-02-06
    Description: Sector-zoned clinopyroxene is common in igneous rocks, but has been overlooked in the study of magmatic processes. Whilst concentric zoning is commonly used as a record of physicochemical changes in the melt feeding crystal growth, clinopyroxene is also highly sensitive to crystallisation kinetics. In sector-zoned crystals, the fidelity of compositional changes as recorders of magma history is dubious and the interplay between thermodynamic and kinetic controls remains poorly understood. Here we combine electron probe and laser ablation micro-chemical maps of titanaugite crystals from Mt. Etna (Sicily, Italy) to explore the origin of sector zoning at the major and trace element levels, and its implications for the interpretation of magmatic histories. Elemental maps afford the possibility to revisit sector zoning from a spatially controlled perspective. The most striking observation is a clear decoupling of elements into sectors vs. concentric zones within single crystals. Most notably, Al-Ti enrichments and Si-Mg depletions in the prism sectors {1 0 0}, {1 1 0} and {0 1 0} relative to the hourglass (or basal) sectors {−1 1 1} correlate with enrichments in rare earth elements and highly charged high field strength elements due to cation exchanges driven by kinetic effects. In contrast, transition metals (Cr, Ni, Sc) show little partitioning into sectors and strong enrichments in concentric zones following resorbed surfaces, interpreted as evidence of mafic recharge and magma mixing. Our results document that kinetic partitioning has minor effects on the compositional variations of cations with low charge relative to the ideal charge/radius of the structural site they occupy in the clinopyroxene lattice. We suggest that this may be due to a lower efficiency in charge balance mechanisms compared to highly charged cations. It follows that compatible metals such as Cr can be considered trustworthy recorders of mafic intrusions and eruption triggers even in sector-zoned crystals. We also observe that in alkaline systems where clinopyroxene crystallisation takes place at near-equilibrium conditions, sector zoning should have little effect on Na-Ca partitioning and in turn, on the application of experimentally calibrated thermobarometers. Our data show that whilst non-sector-zoned crystals form under relatively stagnant conditions, sector zoning develops in response to low degrees of undercooling, such as during slow magma ascent. Thus, we propose that the chemistry of sector-zoned crystals can provide information on magma history, eruption triggers, and possibly ascent rates.
    Description: Published
    Description: 265-283
    Description: 3V. Proprietà chimico-fisiche dei magmi e dei prodotti vulcanici
    Description: JCR Journal
    Repository Name: Istituto Nazionale di Geofisica e Vulcanologia (INGV)
    Type: article
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 6
    Publication Date: 2020-05-28
    Description: The Campi Flegrei caldera (southern Italy) is one of the most hazardous volcanic systems on Earth, having produced 〉60 eruptions in the past 15 ka. The caldera remains active and its potential for future eruptions is high, posing a danger to the dense population living nearby. Despite this, our understanding of pre-eruptive processes and the architecture of the sub-volcanic system are poorly constrained. Here, we combine established petrological techniques, geothermobarometric evaluation, and high resolution trace element crystal mapping, to present a multifaceted, coherent reconstruction of the complex pre eruptive dynamics and eruption timescales of Astroni volcano located in the eastern sector of Campi Flegrei caldera. The Astroni volcano is an important case study for investigating plumbing system processes and dynamics at Campi Flegrei caldera because it produced the most recent (ca. 4 ka ago) Plinian eruption within the caldera (Astroni 6); current long-term forecasting studies postulate that a similar sized event in this location is a probable future scenario. Geothermobarometric results indicate interaction between an evolved, shallow magma chamber, and a less evolved, deeper pocket of magma, in agreement with previous studies focused on the Astroni 6 eruption products. In addition, a range of textural and trace element zoning patterns point to a complex evolution of both magmas prior to their subsequent interaction. High resolution trace element crystal maps reveal discrete zonations in compatible elements. These zonations, combined with knowledge of Kfeldspar growth rates, highlight a recharge event in the shallow plumbing system a few hours to days before the Astroni 6 eruption.
    Description: Published
    Description: 464-477
    Description: 2V. Struttura e sistema di alimentazione dei vulcani
    Description: JCR Journal
    Keywords: Physics - Geophysics ; Physics - Geophysics
    Repository Name: Istituto Nazionale di Geofisica e Vulcanologia (INGV)
    Type: article
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 7
    Publication Date: 2021-12-22
    Description: Systematic variations in the crystal cargo and whole-rock isotopic compositions of mantle-derived basalts in the intraplate Dunedin Volcano (New Zealand) indicate the influence of a complex mantle-to-crust polybaric plumbing system. Basaltic rocks define a compositional spectrum from low-alkali basalts through mid-alkali basalts to high-alkali basalts. High-alkali basalts display clinopyroxene crystals with sector (hourglass) and oscillatory zoning (Mg#61–82) as well as Fe-rich green cores (Mg#43–69), whereas low-alkali basalts are characterized by clinopyroxenes with unzoned overgrowths (Mg#69–83) on resorbed mafic cores (Mg#78–88), coexisting with reversely zoned plagioclase crystals (An43–68 to An60–84 from core to rim). Complex magma dynamics are indicated by distinctive compositional variations in clinopyroxene phenocrysts, with Cr-rich zones (Mg#74–87) indicating continuous recharge by more mafic magmas. Crystallization of olivine, clinopyroxene and titanomagnetite occurred within a polybaric plumbing system extending from upper mantle to mid-crustal depths (485–1059 MPa and 1147–1286°C), whereas crystallization of plagioclase with subordinate clinopyroxene and titanomagnetite proceeded towards shallower crustal levels. The compositions of high-alkali basalts and mid-alkali basalts resemble those of ocean island basalts and are characterized by FOZO-HIMU isotopic signatures (87Sr/86Sri = 0.70277–0.70315, 143Nd/144Ndi = 0.51286–0.51294 and 206Pb/204Pb = 19.348–20.265), whereas low-alkali basalts have lower incompatible element abundances and isotopic compositions trending towards EMII (87Sr/86Sri = 0.70327–70397, 143Nd/144Ndi = 0.51282–0.51286 and 206Pb/204Pb = 19.278–19.793). High- and mid-alkali basalt magmas mostly crystallized in the lower crust, whereas low-alkali basalt magma recorded deeper upper mantle clinopyroxene crystallization before eruption. The variable alkaline character and isotope composition may result from interaction of low-alkaline melts derived from the asthenosphere with melts derived from lithospheric mantle, possibly initiated by asthenospheric melt percolation. The transition to more alkaline compositions was induced by variable degrees of melting of metasomatic lithologies in the lithospheric mantle, leading to eruption of predominantly small-volume, high-alkali magmas at the periphery of the volcano. Moreover, the lithosphere imposed a filtering effect on the alkalinity of these intraplate magmas. As a consequence, the eruption of low-alkali basalts with greater asthenospheric input was concentrated at the centre of the volcano, where the plumbing system was more developed.
    Description: Published
    Description: egab062
    Description: 2V. Struttura e sistema di alimentazione dei vulcani
    Description: 3V. Proprietà chimico-fisiche dei magmi e dei prodotti vulcanici
    Description: 4V. Processi pre-eruttivi
    Description: JCR Journal
    Keywords: alkali basalts ; Dunedin Volcano ; thermobarometry ; primary magma ; lithospheric mantle filter ; Igneous Petrology ; Thermobarometry ; Mantle melting and metasomatism ; Magmatic plumbing systems
    Repository Name: Istituto Nazionale di Geofisica e Vulcanologia (INGV)
    Type: article
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 8
    Publication Date: 2023-10-26
    Description: The Present-day (〈1.2 kyr) activity of Stromboli (Aeolian Islands, Southern Italy) is fed by a vertically-extended mush column with an open-conduit configuration. The eruptive products are the result of periodic supply of mafic magma (low porphyritic or Lp-magma) from depth into a homogeneous shallow reservoir (highly porphyritic or Hp-magma). Clinopyroxene phenocrysts from the 2003–2017 activity exhibit marked diopside-augite heterogeneities caused by continuous Lp-Hp magma mixing and antecryst recycling. Diopsidic bands record Lp-recharge injected into the shallow Hp-reservoir, whereas resorbed diopsidic cores testify to the continuous disruption and cannibalism of relic antecrysts from the mush. The transition between diopside (∼1175 °C) and augite (∼1130 °C) takes place at comparable P (∼190 MPa) and H2O (0.5–2.4 wt%) conditions. Short timescales (∼1 year) for diopsidic bands from the 2003 paroxysm document restricted temporal intervals between mafic injection, magma mixing and homogenization in the Hp-reservoir. Longer timescales (∼4–182 years) for diopsidic cores indicate protracted antecryst remobilization times. By comparing clinopyroxenes from the Present-day and Post-Pizzo eruptions, we argue a distinct phase in the life of Stromboli volcano is evident from the 2003 paroxysm onwards. More efficient mechanisms of mush disruption and cannibalism involve diopsidic antecrysts remobilized and transported by Lp-magmas permeating the mush, in concert with gravitational instability of the solidification front and melt migration within the shallow Hp-reservoir. Magmatic injections feeding the persistent Present-day activity are more intensively mixed and homogenized prior to eruption, reflecting small recharge volumes and/or a more mafic system in which the mafic inputs are less pronounced.
    Description: Published
    Description: 105440
    Description: 3V. Proprietà chimico-fisiche dei magmi e dei prodotti vulcanici
    Description: 4V. Processi pre-eruttivi
    Description: JCR Journal
    Repository Name: Istituto Nazionale di Geofisica e Vulcanologia (INGV)
    Type: article
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 9
    Publication Date: 2023-11-21
    Description: Within subvolcanic plumbing systems, along volcanic conduits and post-eruptive emplacement, mineral textures and compositions are governed by complex kinetic (undercooling) and dynamic (convective) processes that deviate from theoretical models and equilibrium criteria. In this perspective, we have investigated the partitioning of major and trace cations between clinopyroxene and phonotephritic melt under convective stirring conditions at high degrees of undercooling (−ΔTnominal = 30–60 °C) and atmospheric pressure. We have integrated this novel data set with conventional static (no physical perturbation) clinopyroxene-melt compositions obtained under interface- and diffusion-controlled growth regimes. Results show that clinopyroxene growth kinetics and diffusion boundary layers caused by melt supersaturation are partly mitigated by the homogenizing effects of stirring. Because of continuous supply of fresh melt to the advancing crystal surface, the partitioning of major and trace cations is governed by local equilibrium effects, which are interpreted as the extension of equilibrium thermodynamic principles to non-equilibrium bulk systems. Major cations are incorporated into the clinopyroxene structure via the coupled substitution [M1Mg, TSi] ↔ [M1Ti, TAl] and in conformity with the thermodynamic mixing properties of CaMgSiO2, CaAl2SiO6, and CaTiAl2O6 components. The complementary relationship between lattice strain (ΔGstrain) and electrostatic (ΔGelectrostatic) energies of heterovalent substitutions is the most appropriate thermodynamic description for the accommodation of trace cations in the clinopyroxene lattice site (i.e., ΔGpartitioning = ΔGstrain + ΔGelectrostatic). The excess energy of partitioning ΔGpartitioning changes principally with Al in tetrahedral coordination and determines the type and number of charge-balanced and -imbalanced configurations taking place in the structural sites of clinopyroxene. An important outcome from dynamic stirring experiments is that superimposition of convective mass transfer on melt supersaturation phenomena causes the formation of Cr-rich concentric zones under closed system crystallization conditions. However, these Cr-rich zones do not correlate with enrichment in other compatible elements and depletion in incompatible elements, as would be expected in natural open systems characterized by input of more primitive magmas. While the convective transport acts to reduce the diffusive length scale of chemical species in the experimental melt, fresh Cr cations are more easily incorporated into the concentric zones due to crystal field effects. Together, our findings reveal that during magma ascent and emplacement, convective stirring may promote clinopyroxene crystallization and minimize kinetic effects on clinopyroxene zoning.
    Description: Published
    Description: 120531
    Description: 3V. Proprietà chimico-fisiche dei magmi e dei prodotti vulcanici
    Description: JCR Journal
    Repository Name: Istituto Nazionale di Geofisica e Vulcanologia (INGV)
    Type: article
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 10
    Publication Date: 2023-02-21
    Description: Sector-zoned clinopyroxene records kinetic effects imposed by variable degrees of magma undercooling, ΔT, and can be utilised to track the dynamics of magmatic systems. The partitioning of trace elements into sectors grown in different crystallographic orientations can be used as a proxy for ΔT. However, an experimental assessment of the relationship between trace element zoning and ΔT has been lacking to date. Here we present trace element data from a series of undercooling crystallisation experiments on a primitive trachybasalt from Mt. Etna (Italy), at conditions of crustal storage (400 MPa, NNO + 2), and ΔT ranging from 23 to 173 °C. Changes in ΔT were modulated by varying both resting and liquidus temperatures, the latter via the melt-H2O content of the experiments. The resting temperature was retained for 24 h to ensure the attainment of near-equilibrium conditions. High-resolution elemental mapping reveals the distribution of trace elements in individual clinopyroxene zones. Increasing ΔT drives a shift from polyhedral morphologies with Al-rich prism and Al-poor hourglass sectors (ΔT = 23–25 °C), to skeletal (ΔT = 75–123 °C) and dendritic (ΔT = 132–173 °C) crystals with Al-rich skeletons and Al-poor overgrowths. Aluminium-rich zones have higher concentrations of rare earth elements (REE) and high field strength elements (HFSE) than Al-poor zones across all investigated ΔT conditions, and overall, Al, REE and HFSE contents increase with ΔT. This indicates that tetrahedral aluminium (TAl) and associated charge-balancing mechanisms govern the incorporation of REE and HFSE within clinopyroxene. Lattice strain parameters for REE in the M2 site indicate the incorporation of light relative to heavy REE in clinopyroxene is controlled by competing effects between the strain-free partition coefficient, D0, and the optimum cation radius, r0. Critically, the middle and heavy REE switch from incompatible to compatible with increasing ΔT. Used to model fractional crystallisation, our data demonstrate that fractionation of clinopyroxene at low ΔT controls pre-eruptive melt evolution. Importantly, this indicates crystallisation of clinopyroxene in the deep portions of Mt. Etna’s plumbing system is not rapid and is unlikely to result in the early formation of dendrites. We develop a parameterisation of ΔT based on REE partitioning between experimental clinopyroxene and coexisting melt, which can be applied to sector-zoned augite crystallising from mafic alkaline magmas, to reconstruct dynamic processes and thermal pathways during magma transport and storage. Applied to sector-zoned clinopyroxene microphenocrysts and groundmass microcrysts from the 1974 eccentric eruption at Mt. Etna, our parameterisation tracks an increase in ΔT with magma ascent and eruption, following recharge of Cr-rich mafic magma at depth. Sector-zoned clinopyroxene can track ΔT variations leading to volcanism at Mt. Etna and could be applied to quantify magma dynamics in other active volcanoes.
    Description: This work was supported by a Foundation Research Excellence Award from The University of Queensland (UQ-FREA RM2019001828, T.U.), the Advance Queensland Women’s Research Assistance Program from the Queensland Government (WRAP109-2019RD1 RM2020002371, T.U.) and the HP-HT laboratory of Experimental Geophysics and Volcanology (INGV, Rome). A.M. was supported by the Australian Government Research Training Program (RTP). S.M, M.M. and A.P. were supported by the MIUR project “Time scales of solidification in magmas: Applications to Volcanic Eruptions, Silicate Melts, Glasses, Glass- Ceramics” (PRIN 2017J277S9).
    Description: Published
    Description: 249-268
    Description: 3V. Proprietà chimico-fisiche dei magmi e dei prodotti vulcanici
    Description: 4V. Processi pre-eruttivi
    Description: JCR Journal
    Keywords: Clinopyroxene ; Sector Zoning ; Trace element partitioning ; Undercooling ; Dendritic crystals ; Rare earth elements ; LA ICP-MS Mapping ; Mt. Etna ; 04.08. Volcanology
    Repository Name: Istituto Nazionale di Geofisica e Vulcanologia (INGV)
    Type: article
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...