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首页> 外文期刊>Journal of Advances in Modeling Earth Systems >What Controls the Water Vapor Isotopic Composition Near the Surface of Tropical Oceans? Results From an Analytical Model Constrained by Large‐Eddy Simulations
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What Controls the Water Vapor Isotopic Composition Near the Surface of Tropical Oceans? Results From an Analytical Model Constrained by Large‐Eddy Simulations

机译:什么控制热带海洋表面附近的水蒸气同位素组合物?由大涡模拟的分析模型产生的结果

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The goal of this study is to understand the mechanisms controlling the isotopic composition of the water vapor near the surface of tropical oceans, at the scale of about a hundred kilometers and a month. In the tropics, it has long been observed that the isotopic compositions of rain and vapor near the surface are more depleted when the precipitation rate is high. This is called the “amount effect.” Previous studies, based on observations or models with parameterized convection, have highlighted the roles of deep convective and mesoscale downdrafts and rain evaporation. But the relative importance of these processes has never been quantified. We hypothesize that it can be quantified using an analytical model constrained by large‐eddy simulations. Results from large‐eddy simulations confirm that the classical amount effect can be simulated only if precipitation rate changes result from changes in the large‐scale circulation. We find that the main process depleting the water vapor compared to the equilibrium with the ocean is the fact that updrafts stem from areas where the water vapor is more enriched. The main process responsible for the amount effect is the fact that when the large‐scale ascent increases, isotopic vertical gradients are steeper, so that updrafts and downdrafts deplete the subcloud layer more efficiently. Plain Language Summary Water molecules can be light (one oxygen atom and two hydrogen atoms) or heavy (one hydrogen atom is replaced by a deuterium atom). These different molecules are called water isotopes, and their relative concentration in water is called the isotopic composition. The isotopic composition of the precipitation recorded in ice cores or in speleothems can be used to reconstruct past climates. However, the factors controlling the isotopic composition are complex. To better understand these factors, as a first step, we try to understand what controls the isotopic composition of the water vapor near the surface of tropical oceans. It is known to be affected by storm activity. Storms act to deplete the near‐surface water vapor of the heaviest isotopes. To understand how, we use a high‐resolution atmospheric model, with a horizontal grid spacing of 750?m. Such a model explicitly resolves the ascents and descents in the storms and in nearby clouds. We find that storms deplete the near‐surface water vapor mainly because the ascending air export enriched water vapor from the near‐surface to high levels. This conclusion is in contrast with previous studies, which highlighted more the role of descending air and of partial evaporation of the falling?rain.
机译:本研究的目标是了解控制热带海洋表面附近的水蒸气同位素组成的机制,在大约一百公里和一个月的规模。在热带地区,已经观察到,当沉淀率高时,表面附近的雨和蒸汽的同位素组成更加耗尽。这被称为“数量效应”。以前的研究基于具有参数化对流的观测或模型,突出了深度对流和Mesoscale下降和雨蒸发的作用。但这些过程的相对重要性从未被量化。我们假设它可以使用由大涡模拟的分析模型进行量化。大涡模拟的结果确认只有在降水速率变化导致大规模循环中的变化导致的情况下,才能模拟经典量效果。我们发现,与海洋的平衡相比,耗尽水蒸气的主要过程是上升到水蒸气更富含水蒸气的区域。负责数量效应的主要过程是,当大规模上升增加时,同位素垂直梯度是陡峭的,使得上升气流和下降过程更有效地耗尽了副载量。普通语言摘要水分子可以是光(一个氧原子和两个氢原子)或重的(一个氢原子被氘原子取代)。这些不同的分子称为水同位素,它们在水中的相对浓度称为同位素组合物。记录在冰核或斯派科人中的沉淀的同位素组成可用于重建过去的气候。然而,控制同位素组合物的因素是复杂的。为了更好地了解这些因素,作为第一步,我们试图了解热带海洋表面附近的水蒸气的同位素组成。已知受风暴活动的影响。 Storms采取耗尽最重的同位素的近地表水蒸气。要了解如何,我们使用高分辨率大气模型,水平网格间距为750?m。这种模型明确地解析了风暴中的升级和下降和附近的云层。我们发现风暴主要耗尽近地水蒸汽,主要是因为上升的空气出口富含水蒸气从近表面到高水平。这一结论与先前的研究相比,这突出了下降空气的作用和落下的掉落的偏离的作用。

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