Abstract

Aiming to evaluate the influence of pre-existing nuclei on the clinopyroxene crystallization kinetics, time-series experiments were performed using both natural and vitrified starting materials. Experiments were carried out at pressure of 0.8 GPa, temperatures between 1220 and 1250 °C, and dwell times ranging from 0.16 to 12 h. Clinopyroxene growth rates of the runs performed using the natural starting material containing pre-existing nuclei (~2 × 10−7 to ~6 × 10−8 cm∙s−1) are higher than those of the runs performed using the vitrified one (~3 × 10−7 to ~2 × 10−8 cm∙s−1). In both cases the growth rates decrease with increasing time. Conversely, clinopyroxene nucleation rates are lower in the experiments performed using the natural powder (102 and 10 mm−3∙s−1) compared to those performed with the glassy starting material (105 and 103 mm−3∙s−1). The nucleation rates tend to decrease increasing dwell time in all the series up to ~3 h, after which it remains nearly constant. Finally, the combination of the obtained clinopyroxene growth rates with the crystal size analysis of natural clinopyroxenes, allowed to estimate the magma ascent rate and the recharge rate of the Campi Flegrei Volcanic District deep reservoir.

Highlights

  • Knowledge of crystallization kinetics in silicate melts is a fundamental tool in the Earth and material sciences due to the importance of crystallization processes in both natural and synthetic melts [1,2]

  • This study provides constraints on the effect of pre-existing nuclei on clinopyroxene growth and nucleation rates

  • The growth rates calculated in the run performed using natural starting material with pre-existing nuclei are higher than those calculated in the runs performed using the vitrified starting material, while the nucleation rates show the opposite behavior with lower values for the run containing pre-existing nuclei

Read more

Summary

Introduction

Knowledge of crystallization kinetics in silicate melts is a fundamental tool in the Earth and material sciences due to the importance of crystallization processes in both natural and synthetic melts [1,2]. Glassy starting materials (synthetic composition prepared from oxide and carbonate reagents or vitrified natural samples) have the advantage of being completely homogeneous and able to achieve a state of total chemical equilibrium [16,17]; the preparation of these glasses requires multiple fusion cycles at high temperature that strongly affect the nucleation behavior of aluminosilicate melts (e.g., [2,17,18,19]). This is reflected in the experimental products that could be difficult to correlate to crystallization path of natural magmas.

Methods
Results
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call