Effectiveness of Ti-in-amphibole thermometry and performance of different thermometers across lower continental crust up to UHT metamorphism

IF 3.5 2区 地球科学 Q1 GEOCHEMISTRY & GEOPHYSICS Contributions to Mineralogy and Petrology Pub Date : 2024-06-03 DOI:10.1007/s00410-024-02149-6
Omar Bartoli, Bruna B. Carvalho, Federico Farina
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Abstract

Metabasites are important constituents of deep crustal sections and are the favored rock type for studying lower crustal amphibolite to granulite transitions. However, metapelites may develop a larger number of temperature-sensitive mineral assemblages and are particular useful when extreme ultrahigh temperature (UHT) conditions are envisaged. A recent calibration of the Ti-in-amphibole thermometer by Liao et al. (2021) was supposed to make thermometry on metabasites quick and easy to apply. However, their calibration is based on experiments which were not originally designed to investigate in detail the temperature dependence of Ti in amphibole. In addition, a possible effect of aTiO2 and/or pressure on the Ti content of amphibole was not fully taken into account. This resulted in a calibration uncertainty of ± 70 °C (2σ), much higher than that of other single-mineral thermometers. In this study we firstly test the newly calibrated Ti-in-amphibole thermometer across the mid to lower crustal section of the Ivrea–Verbano Zone (IVZ; NW Italy) and compare the performance of different thermometric techniques across the sequence. Ti-in-amphibole thermometry records increasing peak temperatures from amphibolite (600–700 °C), transition (750–800 °C) and granulite (850–950 °C) zones. Titanium content of amphibole may be modified by retrograde fluid influx returning temperatures c. 200–300 °C lower than in non-altered domains. The comparison reveals that Zr-in-rutile thermometer in pelitic granulites seems to be more prone to post-peak resetting than the Ti-in-amphibole thermometry in nearby mafic rocks. This behavior is also confirmed by amphibole analyses from other UHT localities, where the performance of Ti-in-amphibole thermometry is comparable with that of Al-in-orthopyroxene in pelitic granulites. However, Ti-in-amphibole temperatures are underestimated in rutile-bearing samples and this limitation is not solely restricted to rocks containing high H2O contents as previously thought. Derived constraints on the diffusivity of Ti through amphibole demonstrate the robustness of the Ti-in-amphibole thermometer to later thermal disturbances. However, ad-hoc experiments are still necessary to improve the accuracy and precision of calibration and to extend its applicability. This advance will make mafic granulites routine targets for studies devoted to understanding the regional extent of UHT metamorphism.

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Ti-in-闪石测温的有效性和不同测温仪在下大陆地壳直至超高温变质过程中的性能
玄武岩是深地壳剖面的重要组成部分,也是研究下地壳闪长岩向花岗岩转变的首选岩石类型。然而,偏闪长岩可能形成更多对温度敏感的矿物组合,在极端超高温(UHT)条件下尤其有用。Liao 等人(2021 年)最近对闪石中的钛温度计进行了校准,这本应使偏长岩的温度测量快速、简便地得到应用。然而,他们的校准是基于一些实验,而这些实验最初并不是为了详细研究闪石中 Ti 的温度依赖性而设计的。此外,也没有充分考虑到二氧化钛和/或压力对闪石中 Ti 含量可能产生的影响。这导致了 ± 70 °C (2σ) 的校准不确定性,远高于其他单矿物温度计。在这项研究中,我们首先在伊夫雷亚-韦尔巴诺区(IVZ;意大利西北部)的地壳中下部测试了新校准的钛合闪石温度计,并比较了不同测温技术在整个序列中的性能。闪石中的钛测温记录了闪长岩(600-700 °C)、过渡带(750-800 °C)和花岗闪长岩(850-950 °C)区不断升高的峰值温度。闪长岩中的钛含量可能因逆行流体流入而发生变化,返回温度比未发生变化的区域低约 200-300 ℃。比较结果表明,与附近黑云母岩中的闪石钛含量测温法相比,球粒花岗岩中的金红石锆含量测温法似乎更容易发生峰后重置。来自其他超高温炉地点的闪石分析也证实了这一行为,在这些地方,辉绿岩中的钛-闪石测温仪的性能与球粒花岗岩中的铝-正辉石测温仪的性能相当。然而,在含金红石的样品中,钛辉石内温度被低估了,而且这种局限性并不像以前认为的那样仅限于含高浓度 H2O 的岩石。推导出的钛在闪石中的扩散约束条件证明了钛在闪石中温度计对后期热扰动的稳健性。然而,为了提高校准的准确性和精确性并扩大其适用范围,仍有必要进行临时实验。这一进展将使黑云母花岗岩成为了解超高温变质作用区域范围的常规研究目标。
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来源期刊
Contributions to Mineralogy and Petrology
Contributions to Mineralogy and Petrology 地学-地球化学与地球物理
CiteScore
6.50
自引率
5.70%
发文量
94
审稿时长
1.7 months
期刊介绍: Contributions to Mineralogy and Petrology is an international journal that accepts high quality research papers in the fields of igneous and metamorphic petrology, geochemistry and mineralogy. Topics of interest include: major element, trace element and isotope geochemistry, geochronology, experimental petrology, igneous and metamorphic petrology, mineralogy, major and trace element mineral chemistry and thermodynamic modeling of petrologic and geochemical processes.
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