区分青瓷和海绿石用于环境解释:综述

Pragya Singh , Santanu Banerjee , Tathagata Roy Choudhury , Satadru Bhattacharya , Kanchan Pande
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引用次数: 1

摘要

青瓷岩和海绿石在物理、化学和矿物学特征方面具有可比性。这两种矿物的形成都需要在半封闭的微环境中稍微缺氧的条件,以促进Fe吸收到结构中。尽管海绿石在海洋沉积物中普遍存在,但青瓷石在海洋和非海洋环境中都会形成,更常见的是通过改变中镁铁质岩石。对地质柱数据的审查表明,这两种矿物在中生代和新生代更为常见,这可能与广泛的火山活动有关。青瓷石和海绿石的成分变化很大,受孔隙水微环境中阳离子的可用性控制。青瓷的主要元素组成与演化到高度演化的海绿石有很大的重叠。青瓷和海绿石的现有数据和代表性样品揭示了X射线衍射参数和傅里叶变换红外光谱的细微差异。青瓷显示出比海绿石更清晰的基底反射和hkl反射。其特征是在小于1.51Å时表现出明显的11 1’–021、003–022、023和130–13 1’和060反射,表明其晶体结构比海绿石更有序。青瓷石和海绿石的FTIR光谱显示出相似的吸收带,尽管青瓷石中的Si–O弯曲、Si–O拉伸和OH–拉伸带比海绿石更清晰且分辨良好。因此,对于古环境解释,有必要检查X射线衍射参数和FTIR光谱的细微差异,以确认这两种矿物的鉴定。青瓷岩的成分与寄主岩及沉积环境密切相关。与镁铁质岩石伴生的青瓷岩显示出相对较高的Fe、Mg和较低的Al含量。相比之下,那些与长英质至中等成分岩石相关的岩石显示出略高的Al含量和较低的Fe、Mg含量。青瓷岩的矿物化学因海洋和大陆环境而异。海生青瓷的Fe、Mg含量高于非海生青玉,Al含量较低。与富含Fe和Mg的青瓷相比,具有相对较高Al的青瓷可能显示出略低的层间K,用于电荷平衡。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Distinguishing celadonite from glauconite for environmental interpretations: a review

Celadonite and glauconite are comparable in terms of physical, chemical and mineralogical characteristics. Formation of both these minerals requires slightly oxygen-depleted conditions in a semi-confined micro-environment, facilitating the uptake of Fe into the structure. Although glauconite is ubiquitous in marine deposits, celadonite forms in both marine and non-marine environments, more commonly by altering intermediate to mafic rocks. A review of data across the geological column shows that both these minerals are more common in the Mesozoic and Cenozoic, which may be related to extensive volcanism. The composition of celadonite and glauconite is highly variable and is controlled by the availability of cations within the pore water micro-environment. The major element composition of celadonite overlaps with that of evolved to highly evolved glauconite to a large extent. Existing data and representative samples of celadonite and glauconite reveal subtle differences in X-ray diffraction parameters and Fourier transform infrared (FTIR) spectra. Celadonite shows sharper basal and hkl reflections than glauconite. It characteristically exhibits distinct 11 1¯–021, 003–022, 023 and 130–13 1¯, and 060 reflections at less than 1.51 Å, indicating a better-ordered crystallographic structure than glauconite. The FTIR spectra of celadonite and glauconite show similar absorption bands although Si–O bending, Si–O stretching and OH–stretching bands are sharper and well resolved in celadonite than that of glauconite. For palaeoenvironmental interpretations, it is, therefore, necessary to examine the subtle differences in X-ray diffraction parameters and FTIR spectra to confirm the identification of these two minerals. The composition of celadonite relates closely to the host rock and depositional environment. The celadonite associated with mafic rock shows relatively high Fe, Mg and low Al contents. In contrast, those associated with felsic to intermediate composition rocks show slightly higher contents of Al and lower content of Fe, Mg. The mineral chemistry of celadonite varies from marine to continental settings. Marine celadonite contains higher Fe, Mg and lesser Al than their non-marine counterpart. Celadonite with relatively higher Al may show slightly lower interlayer K than Fe and Mg-rich celadonite for charge balancing.

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