Large Water Inventory in Highly Adsorptive Regolith Simulated With a Mars Global Climate Model

IF 4 1区 地球科学 Q1 GEOCHEMISTRY & GEOPHYSICS Journal of Geophysical Research: Planets Pub Date : 2025-02-25 DOI:10.1029/2024JE008697
M. Kobayashi, A. Kamada, T. Kuroda, H. Kurokawa, S. Aoki, H. Nakagawa, N. Terada
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Abstract

This study explores the subsurface water distribution near the surface throughout Mars, using a Mars Global Climate Model (MGCM). We coupled a regolith model that solves the equations of water transport, adsorption, and condensation in the regolith with our MGCM to investigate the effects of inhomogeneous regolith properties on the subsurface water distribution. This regolith model includes a regolith property model that calculates inhomogeneous regolith properties (grain size, porosity, and adsorption coefficient) based on the results of laboratory experiments. The simulations were performed with five different regolith situations over 500 Martian years, aiming for a quasi-steady state of adsorbed water concentration within the top meters of the regolith. Our results revealed a high adsorbed water concentration near the equator (2.0–4.0 kg m−2 for depths within 2 m, with a high adsorption coefficient of ∼200 kg m−3), which was caused by the highly adsorbed regolith, which has a large specific surface area. This indicates the nonnegligible effects of the spatial inhomogeneity of the adsorption coefficient on the adsorbed water distribution. Highly adsorptive regolith also promotes pore ice accumulation in shallower layers at high latitudes because in the winter the freezing of adsorbed water is faster than the water transport in the regolith. In the determination of long-term water retention and runoff on Mars, highly adsorptive regolith acts to retain subsurface water, decelerating water transport within the regolith because the water vapor concentration at equilibrium decreases with increasing adsorption coefficient. This study highlights the significant effects of regolith adsorbability on the subsurface water distribution.

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用火星全球气候模式模拟高吸附性风化层中的大量水
本研究利用火星全球气候模型(Mars Global Climate Model, MGCM)探讨了整个火星地表附近的地下水分布。为了研究非均匀风化层性质对地下水分布的影响,我们将一个求解水在风化层中运移、吸附和凝结方程的风化层模型与我们的MGCM相结合。该风化层模型包括一个风化层性质模型,该模型根据实验室实验结果计算非均匀风化层性质(粒度、孔隙率和吸附系数)。模拟是在5种不同的风化层情况下进行的,时间超过500个火星年,目标是在风化层顶部几米内吸附水浓度的准稳定状态。我们的研究结果表明,赤道附近的吸附水浓度很高(2米深度为2.0-4.0 kg m−2,吸附系数为~ 200 kg m−3),这是由具有大比表面积的高度吸附的风化层引起的。这表明吸附系数的空间不均匀性对吸附水分布的影响不可忽视。高吸附性的风化层也促进了高纬度地区浅层孔隙冰的积累,因为在冬季,被吸附的水的冻结速度快于风化层中的水输送速度。在测定火星上的长期水潴留和径流时,高吸附性的风化层起到了保留地下水的作用,减缓了风化层内的水输送,因为平衡状态下的水蒸气浓度随着吸附系数的增加而降低。该研究强调了表土吸附性对地下水分布的重要影响。
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来源期刊
Journal of Geophysical Research: Planets
Journal of Geophysical Research: Planets Earth and Planetary Sciences-Earth and Planetary Sciences (miscellaneous)
CiteScore
8.00
自引率
27.10%
发文量
254
期刊介绍: The Journal of Geophysical Research Planets is dedicated to the publication of new and original research in the broad field of planetary science. Manuscripts concerning planetary geology, geophysics, geochemistry, atmospheres, and dynamics are appropriate for the journal when they increase knowledge about the processes that affect Solar System objects. Manuscripts concerning other planetary systems, exoplanets or Earth are welcome when presented in a comparative planetology perspective. Studies in the field of astrobiology will be considered when they have immediate consequences for the interpretation of planetary data. JGR: Planets does not publish manuscripts that deal with future missions and instrumentation, nor those that are primarily of an engineering interest. Instrument, calibration or data processing papers may be appropriate for the journal, but only when accompanied by scientific analysis and interpretation that increases understanding of the studied object. A manuscript that describes a new method or technique would be acceptable for JGR: Planets if it contained new and relevant scientific results obtained using the method. Review articles are generally not appropriate for JGR: Planets, but they may be considered if they form an integral part of a special issue.
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