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在基流期间,钙质农业溪流中溶解磷迁移的化学控制。

Chemical controls on dissolved phosphorus mobilization in a calcareous agricultural stream during base flow.

机构信息

Department of Civil and Environmental Engineering, University of Maine, Orono, ME 04469, United States of America.

School of Earth and Climate Sciences, University of Maine, Orono, ME 04469, United States of America.

出版信息

Sci Total Environ. 2019 Apr 10;660:876-885. doi: 10.1016/j.scitotenv.2019.01.059. Epub 2019 Jan 7.

Abstract

This study explores the sources and mechanisms of dissolved phosphorus (P) mobilization under base flow conditions in a headwater stream. We characterized the relevant chemical species and processes within the watershed to investigate connections between stream sediment, surface water, and groundwater with respect to P dynamics. Waters were monitored monthly during the 2017 snow-free period for temperature, pH, dissolved oxygen, conductivity, soluble reactive P (SRP), total P, strong acid anions, strong base cations, dissolved organic carbon (DOC), Al, Fe, and Mn. Phosphorus speciation within sediment samples was determined by sequential chemical extractions. The emerging groundwater was under-saturated by up to 40% with respect to O, with pH = 7.24, T = 7.0 °C, and SRP = 3.0 μg L. Groundwater P was up to ~35× the ambient P (410 ppm). Degassing of CO from the emerging groundwater resulted in a significant increase in pH downstream, and an increase in the SRP concentration from 3.0 to a maximum of 40.6 μg L. Laboratory experiments, using homogenized stream sediment, identified a reduction in the P adsorption capacity, and an increase in desorption of native P with increasing pH from ~7.25 (emerging groundwater) to ~8.50 (air-equilibrated surface water). These data allow us to identify the pH-dependent desorption from P-laden sediment as the most significant source of dissolved P in the headwater stream under base flow conditions.

摘要

本研究探讨了基流条件下一条源头溪流中溶解磷 (P) 迁移的来源和机制。我们对流域内的相关化学物质和过程进行了特征描述,以研究溪流沉积物、地表水和地下水之间与 P 动态有关的联系。在 2017 年无雪期,每月监测一次水温、pH 值、溶解氧、电导率、可溶性反应磷 (SRP)、总磷、强酸阴离子、强碱阳离子、溶解有机碳 (DOC)、Al、Fe 和 Mn。通过连续化学提取法确定沉积物样品中的磷形态。新出现的地下水相对于 O 饱和度不足 40%,pH 值为 7.24,T 值为 7.0°C,SRP 值为 3.0μg/L。地下水中的 P 浓度高达环境 P 的 35 倍左右(410ppm)。从新出现的地下水中脱除 CO 导致下游 pH 值显著升高,SRP 浓度从 3.0 增加到 40.6μg/L 的最大值。使用均匀化的溪流沉积物进行的实验室实验表明,随着 pH 值从7.25(新出现的地下水)增加到8.50(空气平衡的地表水),原生 P 的吸附容量降低,解吸增加。这些数据使我们能够确定基流条件下,带磷沉积物中 pH 依赖性解吸是源头溪流中溶解 P 的最重要来源。

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