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模拟气候变化对流域尺度上农用化学品在水中的归趋和迁移的影响。

Modelling the impacts of climate change on agrochemical fate and transport by water on a catchment scale.

作者信息

Nagesh Poornima, Gassmann Matthias, Eitzinger Josef, de Boer Hugo J, Edelenbosch Oreane Y, van Vuuren Detlef P, Dekker Stefan C

机构信息

Copernicus Institute of Sustainable Development, Utrecht University, Utrecht, the Netherlands.

Department of Hydrology and Substance Balance, University of Kassel, Kassel, Germany.

出版信息

Heliyon. 2024 Aug 3;10(15):e35669. doi: 10.1016/j.heliyon.2024.e35669. eCollection 2024 Aug 15.

Abstract

The export of agrochemicals and their transformation products (TPs) following their application in the agricultural fields poses a threat to water quality. Future changes in climatic conditions (e.g. extreme weather events such as heavy rainfall or extended dry periods) could alter the degradation and mobility of agrochemicals. In this research, we use an integrated modelling framework to understand the impact of extreme climate events on the fate and transport of the agrochemical S-Metolachlor and two of its TPs (M-OXA, Metolachlor Oxanilic Acid and M-ESA, Metolachlor Ethyl Sulfonic Acid). This is done by coupling climate model outputs to the Zin-AgriTra agrochemical reactive transport model in four simulation scenarios. 1) Reference (2015-2018), 2) Very dry (2038-2041), 3) Very wet (2054-2057) and 4) High temperature (2096-2099) conditions of a selected RCP8.5 based regional climate scenario. The modelling framework is tested on an agricultural catchment, Wulka, in Burgenland, Austria. The model results indicate that 13-14 % of applied S-Metolachlor is retained in the soil, and around 85 % is degraded into TPs in the different scenarios. In very dry and high-temperature scenarios, degradation is higher, and hence, there is less S-Metolachlor in the soil. However, a large share of formed M-OXA and M-ESA are retained in the soil, which is transported via overland and groundwater flow, leading to a build-up effect in M-OXA and M-ESA river concentrations over the years. Though a small share of S-Metolachlor and TPs are transported to rivers, their river export is affected by the intensity and amount of rainfall. The very wet and high-temperature scenarios show higher S-Metolachlor and TP concentrations at the catchment outlet due to higher river discharge. The reference scenario shows higher river peak concentrations associated with higher overland flow caused by measured hourly rainfall compared to disaggregated daily precipitation data in the other scenarios.

摘要

农用化学品及其在农田施用后的转化产物(TPs)的排放对水质构成威胁。未来气候条件的变化(如暴雨或长期干旱等极端天气事件)可能会改变农用化学品的降解和迁移情况。在本研究中,我们使用一个综合建模框架来了解极端气候事件对农用化学品S-异丙甲草胺及其两种转化产物(M-OXA,异丙甲草胺草氨酸;和M-ESA,异丙甲草胺乙磺酸)的归趋和迁移的影响。这是通过在四个模拟情景中将气候模型输出与Zin-AgriTra农用化学品反应输运模型耦合来实现的。1)参考情景(2015 - 2018年),2)非常干旱情景(2038 - 2041年),3)非常湿润情景(2054 - 2057年),以及4)基于选定的代表性浓度路径8.5(RCP8.5)区域气候情景的高温情景(2096 - 2099年)。该建模框架在奥地利布尔根兰州的一个农业集水区Wulka上进行了测试。模型结果表明,施用的S-异丙甲草胺有13 - 14%保留在土壤中,在不同情景下约85%降解为转化产物。在非常干旱和高温情景下,降解程度更高,因此土壤中的S-异丙甲草胺含量更低。然而,形成的M-OXA和M-ESA有很大一部分保留在土壤中,它们通过地表径流和地下水流进行迁移,导致多年来M-OXA和M-ESA在河流中的浓度出现累积效应。虽然只有一小部分S-异丙甲草胺和转化产物被输送到河流中,但它们的河流排放受到降雨强度和降雨量的影响。由于河流流量较大,非常湿润和高温情景在集水区出口处显示出更高的S-异丙甲草胺和转化产物浓度。与其他情景中分解的日降水量数据相比,参考情景显示出与实测小时降雨量导致的更高地表径流相关的更高河流峰值浓度。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6cc/11336872/d399bd8d1f24/gr1.jpg

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