The mixing of magmas is a common phenomenon in explosive eruptions. Concentration variance is a useful metric of this process and its decay (CVD) with time is an inevitable consequence during the progress of magma mixing. In order to calibrate this petrological/volcanological clock we have performed a time-series of high temperature experiments of magma mixing. The results of these experiments demonstrate that compositional variance decays exponentially with time. With this calibration the CVD rate (CVD-R) becomes a new geochronometer for the time lapse from initiation of mixing to eruption. The resultant novel technique is fully independent of the typically unknown advective history of mixing – a notorious uncertainty which plagues the application of many diffusional analyses of magmatic history. Using the calibrated CVD-R technique we have obtained mingling-to-eruption times for three explosive volcanic eruptions from Campi Flegrei (Italy) in the range of tens of minutes. These in turn imply ascent velocities of 5-8 meters per second. We anticipate the routine application of the CVD-R geochronometer to the eruptive products of active volcanoes in future in order to constrain typical “mixing to eruption” time lapses such that monitoring activities can be targeted at relevant timescales and signals during volcanic unrest.
The mobility of chemical elements in magmas plays a key role in the homogenization of the compositional gradients that attend the processes of magma differentiation. The action of chemical gradients and their homogenization in the melt phase influences, for example, the rates of crystallization, assimilation of country rocks and magma mixing. The latter is a ubiquitous petrologic process involved in planetary evolution1,2,3,4,5,6. Magma mixing is also recognized to be a major process in generating extreme compositional variations in magmas5,7,8. It is also commonly associated with highly explosive volcanic eruptions9,10,11,12. Its detailed understanding is therefore of primary importance for petrology and volcanology, with direct implications for volcanic monitoring during volcano unrest and as a consequence, for hazard mitigation planning and risk analysis.
In principle the rate of homogenization of compositional gradients in natural melts can be quantified by chemical diffusion modeling13,14,15,16. Such quantification however requires a comprehensive model of multicomponent melt diffusion and a knowledge of the advective history of the mingling magmatic system. The former is highly underconstrained by current models. The models that have been proposed to account for the multi-component nature of diffusion processes in igneous systems16,17,18 are typically based on the modeling of three or four components. Natural silicate melts contain far more relevant chemical species. The lack of a general model, accounting for the role of all chemical components and their interdependence in dynamic systems, significantly hinders our understanding of magmatic systems. The latter is an even greater problem as the advective history of mingling magmas is a chaotic process which cannot be unravelled by attempting to numerically “undo” the process of magmatic flow. The new methods presented here, based on the concept of the time decay of the variance of chemical composition during mingling, frees us from both of the above constraints in estimating the timescale of the mingling process.
Time-series magma mixing experiments
Here we perform a novel assessment of element mobility and chemical homogenization in silicate melt systems via the concept of Concentration Variance Decay (CVD). This new analysis is applied here to time-series experiments performed on mixing volcanic melts using a high-temperature (1,200 °C) centrifuge furnace (Fig. 1).
The initial compositions of end-members were an alkali basalt and a phonolite from the Campi Flegrei volcanic system (Italy)19. The centrifugal force exerted by rotation has accelerated the injection of the basalt into the phonolite (see Methods section). During injection tendrils of basalt are entrained into the phonolite triggering a “fountain-like” process of mingling. This configuration of the experimental sample and the resulting mixing dynamics are intended to simulate the triggering of magma mixing in nature via injection of mafic magmas into felsic magma chambers20,21. The time evolution of the mixing process results in the progressive mixing of the tendrils of basaltic melt with the phonolitic melt (Fig. 1).
The mixing patterns observed may be described as filaments, swirls and bands ranging down to the micron length scale. These morphologies and length scales are topologically similar to those observed in natural rock samples where the mingling has been frozen-in4. The mixing process results in a transition from initially sharp chemical fluctuations oscillating between the two end-member compositions (Fig. 2) through progressive reduction of the amplitude and variability of these chemical fluctuations, to a final homogeneous hybrid composition (Fig. 2 and Supplementary Dataset).
We evaluated the degree of homogeneity of the mixture using the normalized concentration variance
where and are the concentration variances of a given chemical element (Ci) at time t (corresponding to the duration of the experiment) and time t = 0, respectively. Specifically, we calculated sample variance for the transects and population variance for the end-members; this procedure has been used consistently for both experimental and natural samples (see below). We observe that decreases rapidly, relaxing towards zero within 120 minutes (Fig. 3). The Concentration Variance Decay (CVD) for all chemical elements was fitted using the Matlab® software by an exponential function of the form
where C0, R and C1 are fitting parameters and t is the mixing time. The values of fitting parameters are reported in Table 1. The rate R at which concentration variance decays (CVD-R) is a metric quantifying element mobility during mixing (Fig. 3).
In Fig. 4 the estimated values of the rate of CVD (R) for all analyzed chemical elements are plotted against their ionic radii. Several observations can be made. Na shows the highest mobility, followed by Al. The other major elements (i.e. Mg, Ca, K, Si, Ti and Fe) show R values in the range 0.11–0.08. That same interval of R values is exhibited by several trace elements such as Nb, Ta, Zr, Hf, U, Th, Eu, Sr, Ba, Rb and Cs. Rare Earth Elements (REEs) display a distinct behavior: i) their R values are lower and ii) R decreases progressively with ionic radius. The exception to this trend is Eu whose R is comparable with the other elements (Fig. 4).
It is somewhat instructive to observe correlations between the results of the CVD-R and published tracer or self-diffusion data. Where data exist, the mobilities tracked in this study can be compared with coefficients of diffusivity in multicomponent systems. Note that as of yet virtually no systematic studies report the diffusion coefficients for the complete set of relevant major and trace elements in natural melts and thus our comparison is, at best, a partial one. The major alkalis (i.e. Na and K) have much larger diffusion coefficients relative to the other major elements13,14. Our results corroborate this behavior for Na, but not for K. The melts analyzed in Baker13,14 have maximum K2O contents of ca. 4%. The content of K2O in the melts from Campi Flegrei used in our experiments is higher (up to ca. 8%). It has been shown13 that the diffusion coefficient of a chemical element has the tendency to decrease with the abundance of the same element in the melt. This may explain why K displays a lower mobility than Na in our melts. As for the other major elements, the limited variation in R reflects similar mobility (Fig. 4), in agreement with known diffusivities13,14.
Systematic studies of trace element diffusivities are few22,23,24. Available data indicate that Rb, Sr and Ba have the highest values of diffusivities; whereas diffusivity values for REEs are lower22,23,24, in agreement with our results (Fig. 4). However, for the case of element diffusivity in jadeitic melts, U and Th have been shown to have the lowest diffusivities24, contrary to what we observe. Nb, Ta, Zr and Hf, are generally regarded as slowly diffusing species22,24. In apparent contrast our results demonstrate that their high R values are similar to those estimated for Th, Sr, or Rb. The systematic decrease of R values from light to heavy REEs is in general agreement with literature data22,24. As for Eu, it can be present in the divalent state in silicate melts, while the other REEs occur only in the trivalent state. This presumably yields a larger mobility for Eu22,24.
The above analysis illustrates that, whereas some elements exhibit similarities between R and the diffusion coefficient, others do not. This fact highlights that diffusion coefficients estimated for individual melts can in general not be robustly applied to the study of the space and time complexity generated by mixing processes. In contrast, the use of CVD-R values incorporates, in a single variable, the sum of a range of processes that affect element mobility, including: 1) partitioning of chemical elements into structurally different melts25, 2) the dependence of diffusivities on multicomponent composition16, 3) the influence of advection on apparent diffusive fluxes26 and 4) the potential development of “uphill” diffusion patterns15. Thus the variable R provides a first order cumulative assessment of element mobility. It does not of course identify the dominant mechanisms driving elemental diffusion. The understanding of the interplay of all the variables influencing element mobility will likely require combined thermodynamic- and fluid dynamic-based numerical simulations in future.
Estimate of mixing-to-eruption time
We now apply the CVD-R method to the Campi Flegrei system in order to estimate the timescales of magma mixing immediately preceding eruptions (i.e. the mixing-to-eruption time interval). Note that the rationale we employ here (using experimental data to make inferences about natural processes) is based on the consideration that the space and time evolution of magma mixing processes is governed by the development of chaotic dynamics. This assertion is well-substantiated in previous studies employing natural samples4,27, numerical simulations28,29 and experiments7,30. The stretching and folding dynamics of fluid elements, responsible for the development of chaotic dynamics, are also responsible for the production of scale-invariant fractal structures. This results in the generation of self-similar compositional domains propagating in the magmatic mass over several orders of magnitude28,31. It has, for example, been demonstrated that compositional heterogeneity generated by magma mixing propagates from the meter to the micron length-scale4. It follows that magmatic systems can be analyzed at any length scale and they will provide, statistically, the same type of information. Importantly, this justifies the use of smaller experimental samples in the effort to explain natural processes on a much wider range of scales.
The concentration variance  was calculated (Table 1) for each analyzed chemical element in three pyroclastic sequences which correspond to three explosive eruptions (Averno, Astroni and Agnano-Monte Spina) of the Campi Flegrei volcanic system (Italy)19 where magma mixing is extraordinarily well-documented32. The three sequences are geochemically zoned (Fig. 5) indicating the occurrence of compositional gradients in these volcanic systems and highlighting the contemporaneous presence of melts with different compositions (with more mafic magmas underlying more evolved magmas) (see Supplementary Dataset). Small-scale compositional fluctuations (of the order of a few tens of centimeters) along the pyroclastic sequences also provide evidence for the action of mixing dynamics acting in the plumbing systems before the onset of eruptions. The plots display the current position of samples in the stratigraphic sequences (so that they need to be reversed to visualize the chemical zoning in the original magma reservoirs). To estimate the mixing time we first calculated the variance values for each chemical element measured on natural samples (see Methods section; Table 1). Next, using the exponential empirical relationships derived from experiments for each element, the mixing time was estimated (Table 1). Results indicate that mixing lasted for 18 ± 5 (s.d.), 13 ± 4 (s.d.) and 15 ± 4 (s.d.) minutes for Averno, Astroni and Agnano-Monte Spina events, respectively. These estimates are statistically robust as they are based on a large number of chemical elements converging to short timescales. We nevertheless further tested the robustness of our statistical analysis by randomly removing from the pyroclastic sequences a progressively increasing number of samples. Results indicate that timescales can be estimated with an uncertainty comparable to the uncertainty resulting from averaging the time estimates for all chemical elements (i.e. of the order of ± 4–5 min s.d.). This holds for removing up to 75% of the data from the three stratigraphic sections. If a larger percentage of samples is removed, time estimates start to fluctuate as the number of samples become subcritical with respect to representativeness. This implies that, for example, in the case of the Averno pyroclastic sequence, collecting about 15 samples in the stratigraphic section is enough to obtain robust mixing-to-eruption timescales.
Previously33 the Averno and Astroni events were suggested to have mixing-to-eruption times on the order of days. These times are now shifted to tens of minutes on the basis of our experimental calibration. We believe that these new timescales are more realistic. In particular, previous mixing experiments were performed by placing a phonolite on the top of a trachyte and stirring using a spindle vertically positioned into the crucible33. Given the gravitationally stable configuration (denser trachyte at the bottom and lighter phonolite at the top) there was little chance for mixing. In particular, mixing occurred essentially at the interface between the two melts by diffusion. This was reflected in longer timescales. The new experiments presented here were performed by injecting the basalt into the phonolite. This is considered as the main mechanism for the replenishment and mixing in natural magma chambers20,21. This process generated a large amount of contact interfaces between the two melts, increasing chemical exchanges, as observed in several natural samples showing magma mixing patterns4,28,34. In addition, these two compositions have been envisaged as the most likely end-members participating to magma mixing processes in the Campi Flegrei volcanic area35. Therefore, we are prone to believe that, given the more realistic conditions of the new experiments, these timescales are more robust than previous one.
Timescales obtained in this work indicate that very little time elapsed from the moment mixing started to eruption. These results are in agreement with recent numerical simulations of magma mixing36 that highlight mixing timescales of a few hours to attain complete hybridization of magmas for the Campi Flegrei magmatic systems. Our results constrain mixing durations before eruption to tens of minutes. Establishing whether the mixing process caused the eruptions or vice versa is not easy (for example the ascent of magmas towards the Earth’s surface may have provoked mixing of stratified plumbing systems). In both cases, however, estimating the mixing-to-eruption duration is highly valuable as it provides unprecedented information about the timing elapsing between the beginning of instability in the plumbing system and the eruption. Estimates of the location of the shallow magma reservoirs that were involved in the recent eruptive activity of the Campi Flegrei volcanic systems studied here indicate depths around four to five kilometers37,38. This implies average ascent velocities of the magma of the order of 5–8 meters per second and point to very rapid magma ascent through the sub-volcanic systems. These ascent velocities are of the same order of magnitude as those recently estimated, for example, for calc-alkaline rhyolitic magmas (ca. 1 m/s)39. The slightly higher ascent velocity values derived here can possibly be explained by the fact that K-alkaline magmas from Campi Flegrei have lower viscosities compared to calc-alkaline rhyolitic magmas. The higher alkali contents lead to a strongly reduced viscosity of Campi Flegrei magmas favoring higher ascent velocities. These ascent velocities are also very close to the fragmentation front velocities achievable due to decompression fragmentation, a necessary condition for sustained eruptive flow40. In addition and perhaps most importantly, these magma bodies experienced mixing processes: the introduction of hot and low viscosity mafic melts into higher viscosity melts may have promoted fluidization of the magmatic mass12 and heating due to the retrograde solubility of H2O41,42, further accelerating their migration towards the surface.
These results have implications for civil protection planning of future volcanic crisis because these high velocities of ascending magmas may imply little warning in volcanic crises.
It is important to note that the method we propose to estimate the mixing-to-eruption timescale has been tested using end-members from the Campi Flegrei and applied to the same volcanic system. If the end-member compositions are changed, the rheological properties and the relative mobility of the elements can change. Substantially different end-member couples require new experiments to derive empirical relationships to be used to infer the mixing-to-eruption timescales for other magmatic/volcanic systems.
We anticipate our findings to be a starting point towards a unifying model explaining chemical exchanges in magmatic systems and supplying information on the use of chemical element mobility as geochronometers for volcanic eruptions. This may provide unparalleled clues for building an inventory of past and recent volcanic eruption timescales and could be decisive for hazard assessment in active volcanic areas.
Natural end-members used in the experiments come from Agnano Monte-Spina B1-B2 phonolitic tuff and the glass matrix of the alkali-basalt from Minopoli (Campi Flegrei volcanic area, Italy)43. These compositions are considered as suitable end-members for magma mixing processes in the study area35. The values of measured viscosity and calculated density of the basaltic and the phonolitic melt at 1200 °C are ca. 200 and 20000 Pas and 2.82 and 2.50 g/cm3, respectively. Starting materials for the experiments have been prepared by melting these natural products. End-members were completely homogenized at 1,400 °C in a NaberthermTM furnace for 24 hours. Successively, the homogeneity and the absence of crystals in the samples were tested. Glass cylinders with 0.5 cm height and 0.5 cm diameter were drilled, polished on both sides and mounted, one on top of the other, inside a Pt-capsule (diameter, d = 0.5 cm; length, l = 1.0 cm). The Pt-capsule was sealed on the top and the bottom leaving a small (ca. 0.5 mm) aperture to allow for eventual gas release. The relative mass fractions of the phonolitic and basaltic melts for the experiments were 50%–50%.
The centrifuge used to perform the experiments is a Cryofuge 8500i (Heraeus InstrumentsTM) modified to host a high-temperature furnace (up to 1,200 °C). Three Pt–PtRh10 (type S- Kanthal™ wire) thermocouples were used to monitor the temperature at the top, bottom and the middle of the Pt-capsule containing the samples. A slip-ring assemblage provided the electric power supply and thermocouple reading from the furnace. Sliding electrical contacts (copper rings and brass-carbon brushes from Kontakt-Kohlen Kever, Koln) of the slip-ring assemblage consist of a rotating central section (rings) and a stationary outer section (brushes). More details about the machine are reported in Dorfman et al.44. Before running the experiment the slip-ring assemblage was mounted on the shaft of the centrifuge. This machine was used in the past for different purposes (e.g. measurements of viscosity using the falling-sphere method, experiments of unmixing using basaltic magma) and detailed technical information are reported in Dorfman et al.44 and Veksler et al.45.
The Pt-capsules containing the end-members were then introduced into the outer container of the centrifuge. The same conditions were used for all experiments. A rotation speed (n) of 1850 rpm was used to perform experiments at the temperature of 1,200 °C. We performed three experiments at different times: 5, 20 and 120 minutes.
Experiments were performed at Reynolds number (Re) of the order of 10−10. Experiments, therefore, were performed under laminar fluid dynamics conditions as these conditions are likely to prevail in magmatic systems46,47. Re was calculated as reported in Yuan and Zheng48.
where Fc = ρVω2Rc is the centrifugal force, ρ is density, V is the volume of the capsule, ω is the angular velocity of the centrifuge, Rc is the distance between the experimental capsule and the center of rotation of the centrifuge (i.e. 26.5 cm), l and d are the length and the diameter of the capsule and μ is viscosity. Average values of density (ρ) and viscosity (μ) were calculated considering the initial proportions of end-members (i.e. 50%–50%).
At the end of experiments the samples were quenched in air by turning off the centrifuge rotation and the heating. During quenching, the temperature of the sample dropped from 1,200 to 1,100 °C in 10 s, from 1,100 to 1,000 °C in 15 s; further cooling to 800 °C required approximately 1.5–2 minutes. The experimental samples were then cut in the middle part and prepared for optical inspections, electron microprobe and ICP-MS-Laser Ablation analyses.
Major and trace elements were measured on an average of 100 data points along each electron microprobe at the Department of Earth and Environmental Sciences, LMU-Munich. Analytical conditions were: 15 kV acceleration voltage and 20 nA beam current. In order to avoid alkali loss during analyses a defocused 10-μm beam was used. Synthetic wollastonite (Ca, Si), periclase (Mg), corundum (Al), natural orthoclase (K) and albite (Na) were used as standards. The PAP procedure49 was used to perform the matrix correction. For all analyzed elements standard deviations were lower than 2.5%. Trace elements determinations were performed using the Laser Ablation ICP-MS microanalysis facility installed at the Department of Physics and Geology of the University of Perugia (Italy)50. Analyses were performed using a spot size of 40 μm; consecutive data points were analyzed with a spacing of 40 μm. This allowed us to appreciate in details the compositional variability in the studied experiments. Analytical precision was better than 10% (s.d.) for all analyzed elements51.
The total number of analyzed natural samples for Astroni (Astroni 6 eruption)33, Averno (Averno 2 eruption)33 and Agnano-Monte Spina37 pyroclastic sequences was 36, 62 and 38, respectively. Samples are mostly glassy with a few crystals of ca. 6%, 3% and 4% for Astroni, Averno and Agnano-Monte Spina, respectively. We consider this crystal contents having a negligible effect on the chemical variability of natural rocks compared to the variability triggered by the magma mixing process. Each sample consists of several (10-15) pumice fragments collected in the same stratigraphic level33. Details on sample preparation for geochemical analysis are given in Perugini et al.33. Major elements were analyzed by combined X-ray fluorescence and wet chemical techniques. Trace elements were analyzed by LA-ICP-MS graphite electrode tetraborate fusion by using the method described in Petrelli et al.50,51 at the Department of Physics and Geology, University of Perugia (Italy). Normalized concentration variance for each element used in the estimate of mixing-to-eruption timescale was calculated as the ratio between the concentration variance among all samples and the variance between the two most extreme compositions found in the stratigraphic sequence.
How to cite this article: Perugini, D. et al. Concentration variance decay during magma mixing: a volcanic chronometer. Sci. Rep. 5, 14225; doi: 10.1038/srep14225 (2015).
Abe, Y. Thermal and chemical evolution of the terrestrial magma ocean. Phys. Earth Planet. Inter. 100, 27–39 (1997).
Anderson, D. L. Isotopic evolution of the mantle: the role of magma mixing. Earth Planet. Sci. Lett. 57, 1–12 (1982).
Kratzmann, D. J., Carey, S., Scasso, R. & Naranjo, J. A. Compositional variations and magma mixing in the 1991 eruptions of Hudson volcano, Chile. Bull. Volcanol. 71, 419–439 (2009).
Perugini, D., Poli, G. & Mazzuoli, R. Chaotic advection, fractals and diffusion during mixing of magmas: Evidence from lava flows. J. Volcanol. Geotherm. Res. 124, 255–279 (2003).
Slaby, E. et al. Chaotic three-dimensional distribution of Ba, Rb and Sr in feldspar megacrysts grown in an open magmatic system. Contrib. To Mineral. Petrol. 162, 909–927 (2011).
Morgavi, D., Perugini, D., De Campos, C. P., Ertel-Ingrisch, W. & Dingwell, D. B. Time evolution of chemical exchanges during mixing of rhyolitic and basaltic melts. Contrib. to Mineral. Petrol. 166, 615–638 (2013).
De Campos, C. P., Perugini, D., Ertel-Ingrisch, W., Dingwell, D. B. & Poli, G. Enhancement of magma mixing efficiency by chaotic dynamics: an experimental study. Contrib. To Mineral. Petrol. 161, 863–881 (2011).
Perugini, D., De Campos, C. R., Dingwell, D. B., Petrelli, M. & Poli, G. Trace element mobility during magma mixing: Preliminary experimental results. Chem. Geol. 256, 146–157 (2008).
Druitt, T. H., Costa, F., Deloule, E., Dungan, M. & Scaillet, B. Decadal to monthly timescales of magma transfer and reservoir growth at a caldera volcano. Nature 482, 77–97 (2012).
Leonard, G. S., Cole, J. W., Nairn, I. A. & Self, S. Basalt triggering of the c. AD 1305 Kaharoa rhyolite eruption, Tarawera Volcanic Complex, New Zealand. J. Volcanol. Geotherm. Res. 115, 461–486 (2002).
Martin, V. M. et al. Bang! Month-scale eruption triggering at Santorini volcano. Science 321, 1178 (2008).
Kent, A. J. R., Darr, C., Koleszar, A. M., Salisbury, M. J. & Cooper, K. M. Preferential eruption of andesitic magmas through recharge filtering. Nat. Geosci. 3, 631–636 (2010).
Baker, D. R. Chemical Interdiffusion of Dacite and Rhyolite - Anhydrous Measurements at 1 Atm and 10 Kbar, Application of Transition-State Theory and Diffusion in Zoned Magma Chambers. Contrib. To Mineral. Petrol. 104, 407–423 (1990).
Baker, D. R. Interdiffusion of Hydrous Dacitic and Rhyolitic Melts and the Efficacy of Rhyolite Contamination of Dacitic Enclaves. Contrib. To Mineral. Petrol. 106, 462–473 (1991).
Watson, E. B. & Jurewicz, S. R. Behavior of alkalies during diffusive interaction of granitic xenoliths with basaltic magma. J. Geol. 92, 121–131 (1984).
Zhang, Y. Geochemical kinetics. (Princeton Univ Press, 2008).
Chakraborty, S., Dingwell, D. B. & Rubie, D. C. Multicomponent diffusion in ternary silicate melts in the system K2 O-Al2O3-SiO2: II. Mechanisms, systematics and geological applications. Geochim. Cosmochim. Acta 59, 265–277 (1995).
Liang, Y., Richter, F. M. & Chamberlin, L. Diffusion in silicate melts: III. Empirical models for multicomponent diffusion. Geochim. Cosmochim. Acta 61, 5295–5312 (1997).
Civetta, L. et al. Geochemical zoning, mingling, eruptive dynamics and depositional processes - The Campanian Ignimbrite, Campi Flegrei caldera, Italy. J. Volcanol. Geotherm. Res. 75, 183–219 (1997).
Campbell, I. H. & Turner, J. S. The Influence of Viscosity on Fountains in Magma Chambers. J. Petrol. 27, 1–30 (1986).
Jellinek, A. M., Kerr, R. C. & Griffiths, R. W. Mixing and compositional stratification produced by natural convection 1. Experiments and their application to Earth’s core and mantle. J. Geophys. Res. Earth 104, 7183–7201 (1999).
Behrens, H. & Hahn, M. Trace element diffusion and viscous flow in potassium-rich trachytic and phonolitic melts. Chem. Geol. 259, 63–77 (2009).
Mungall, J. E., Dingwell, D. B. & Chaussidon, M. Chemical diffusivities of 18 trace elements in granitoid melts. Geochim. Cosmochim. Acta 63, 2599–2610 (1999).
Nakamura, E. & Kushiro, I. Trace element diffusion in jadeite and diopside melts at high pressures and its geochemical implication. Geochim. Cosmochim. Acta 62, 3151–3160 (1998).
Watson, E. B. Two-liquid partition coefficients: Experimental data and geochemical implications. Contrib. To Mineral. Petrol. 56, 119–134 (1976).
Perugini, D., Petrelli, M. & Poli, G. Diffusive fractionation of trace elements by chaotic mixing of magmas. Earth Planet. Sci. Lett. 243, 669–680 (2006).
Flinders, J. & Clemens, J. D. Non-linear dynamics, chaos, complexity and enclaves in granitoid magmas. Trans. R. Soc. Edinburgh-Earth Sci. 87, 217–223 (1996).
Perugini, D., Ventura, G., Petrelli, M. & Poli, G. Kinematic significance of morphological structures generated by mixing of magmas: a case study from Salina Island (southern Italy). Earth Planet. Sci. Lett. 222, 1051–1066 (2004).
Petrelli, M., Perugini, D. & Poli, G. Transition to chaos and implications for time-scales of magma hybridization during mixing processes in magma chambers. Lithos 125, 211–220 (2011).
Perugini, D., De Campos, C. P., Ertel-Ingrisch, W. & Dingwell, D. B. The space and time complexity of chaotic mixing of silicate melts: Implications for igneous petrology. Lithos 155, 326–340 (2012).
Morgavi, D., Perugini, D., Campos, C. P. De, Ertel-Ingrisch, W. & Dingwell, D. B. Morphochemistry of patterns produced by mixing of rhyolitic and basaltic melts. J. Volcanol. Geotherm. Res. 253, 87–96 (2013).
Pappalardo, L., Piochi, M., D’Antonio, M., Civetta, L. & Petrini, R. Evidence for multi-stage magmatic evolution during the past 60 kyr at Campi Flegrei (Italy) deduced from Sr, Nd and Pb isotope data. J. Petrol. 43, 1415–1434 (2002).
Perugini, D., Poli, G., Petrelli, M., De Campos, C. P. & Dingwell, D. B. Time-scales of recent Phlegrean Fields eruptions inferred from the application of a ‘diffusive fractionation’ model of trace elements. Bull. Volcanol. 72, 431–447 (2010).
Wada, K. Fractal Structure of Heterogeneous Ejecta from the Me-Akan Volcano, Eastern Hokkaido, Japan - Implications for Mixing Mechanism in a Volcanic Conduit. J. Volcanol. Geotherm. Res. 66, 69–79 (1995).
Arienzo, I., Civetta, L., Heumann, A., Worner, G. & Orsi, G. Isotopic evidence for open system processes within the Campanian Ignimbrite (Campi Flegrei-Italy) magma chamber. Bull. Volcanol. 71, 285–300 (2009).
Montagna, C. P., Papale, P. & Longo, A. Timescales of mingling in shallow magmatic reservoirs. Geol. Soc. London, Spec. Publ. 422, SP422.6; 10.1144/SP422.6 (2015).
Arienzo, I., Moretti, R., Civetta, L., Orsi, G. & Papale, P. The feeding system of Agnano-Monte Spina eruption (Campi Flegrei, Italy): Dragging the past into present activity and future scenarios. Chem. Geol. 270, 135–147 (2010).
Di Renzo, V. et al. The magmatic feeding system of the Campi Flegrei caldera: Architecture and temporal evolution. Chem. Geol. 281, 227–241 (2011).
Castro, J. M. & Dingwell, D. B. Rapid ascent of rhyolitic magma at Chaiten volcano, Chile. Nature 461, 780–783 (2009).
Richard, D., Scheu, B., Mueller, S. P., Spieler, O. & Dingwell, D. B. Outgassing: Influence on speed of magma fragmentation. J. Geophys. Res. Solid Earth 118, 862–877 (2013).
Russell, J. K. Magma mixing processes: insights and constraints from thermodynamic calculations. Rev. Mineral. Geochemistry 24, 153–190 (1990).
Ryan, A. G., Russell, J. K., Nichols, A. R. L., Hess, K.-U. & Porritt, L. A. Experiments and models on H2O retrograde solubility in volcanic systems. Am. Mineral. 100, 774–786 (2015).
De Vita, S. et al. The Agnano-Monte Spina eruption (4100 years BP) in the restless Campi Flegrei caldera (Italy). J. Volcanol. Geotherm. Res. 91, 269–301 (1999).
Dorfman, A., Hess, K. U. & Dingwell, D. Centrifuge-assisted falling-sphere viscometry. Eur. J. Mineral. 8, 507–514 (1996).
Veksler, I. V., Dorfman, A. M., Borisov, A. A., Wirth, R. & Dingwell, D. B. Liquid immiscibility and the evolution of basaltic magma. J. Petrol. 48, 2187–2210 (2007).
Glazner, A. F. Magmatic life at low Reynolds number. Geology 42, 935–938 (2014).
Girard, G. & Stix, J. Buoyant replenishment in silicic magma reservoirs: Experimental approach and implications for magma dynamics, crystal mush remobilization and eruption. J. Geophys. Res. 114, B08203; 10.1029/2008JB005791 (2009).
Yuan, L. A. & Zheng, Y. F. A Microdevice for the Mixing of a Highly Viscous Biosample With Water/Membrane Protein Solution Using Microchannel and Centrifugation. Jala 16, 68–81 (2011).
Pouchou, L. & Pichoir, F. A new model for quantitative X-ray microanalysis: Part I: applications to the analysis of homogeneous samples. Rech. Aerospatielle 3, 13–38 (1984).
Petrelli, M., Perugini, D., Poli, G. & Peccerillo, A. Graphite electrode lithium tetraborate fusion for trace element determination in bulk geological samples by laser ablation ICP-MS. Microchim. Acta 158, 275–282 (2007).
Petrelli, M., Perugini, D., Alagna, K. E., Poli, G. & Peccerillo, A. Spatially resolved and bulk trace element analysis by laser ablation - inductively coupled plasma - mass spectrometry (LA-ICP-MS). Period. Di Mineral. 77, 3–21 (2008).
We are grateful for funding from the Alexander von Humboldt Stiftung (DP), DFG-ICDP project DI 431/31-1, AOBJ: 564369, a research professorship of the Bundesexzellenzinitiative (LMUexcellent), the Advanced Investigator ERC grant 247076 EVOKES (DBD), the Consolidator ERC grant 612776 CHRONOS (DP), Deutsche Forschungsgemeinschaft project GZ-CA 905/1-1 (CDC and DBD). FAPESP provided a Visiting Professor grant regular project 2015/118500 and thematic project (2009/50493-8) (CDC). We thank A. Dorfman for the help in preparing the experiments. Y. Lavallée provided comments that greatly improved the manuscript.
The authors declare no competing financial interests.
About this article
Cite this article
Perugini, D., De Campos, C., Petrelli, M. et al. Concentration variance decay during magma mixing: a volcanic chronometer. Sci Rep 5, 14225 (2015). https://doi.org/10.1038/srep14225
High-K calc-alkaline to shoshonitic intrusions in SE Tibet: implications for metasomatized lithospheric mantle beneath an active continental margin
Contributions to Mineralogy and Petrology (2021)
Geochemical and Sr–Nd isotopic features of the Zaro volcanic complex: insights on the magmatic processes triggering a small-scale prehistoric eruption at Ischia island (south Italy)
International Journal of Earth Sciences (2020)
Scientific Reports (2019)
Pre-eruptive conditions and triggering mechanism of the ~ 16 ka Santa Bárbara explosive eruption of Sete Cidades Volcano (São Miguel, Azores)
Contributions to Mineralogy and Petrology (2019)
Timescales of water accumulation in magmas and implications for short warning times of explosive eruptions
Nature Communications (2018)