4.8 Review

Insight into the distribution of pharmaceuticals in soil-water-plant systems

期刊

WATER RESEARCH
卷 152, 期 -, 页码 38-46

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.watres.2018.12.039

关键词

Plant uptake; Soil pore water; Bioavailability; Bioaccumulation; Translocation

资金

  1. Agriculture and Food Research Initiative Competitive Grant from USDA National Institute of Food and Agriculture [2016-67017-24514]
  2. Michigan AgBioResearch Project GREEEN
  3. NIFA [810866, 2016-67017-24514] Funding Source: Federal RePORTER

向作者/读者索取更多资源

Pharmaceuticals in agricultural soils originating from irrigation with treated wastewater and land applied biosolids can enter field crops. However, little is known about the role of pore water in plant uptake of pharmaceuticals from soils. In this study, the fate, uptake and distribution of fifteen commonly used pharmaceuticals in soil-water-radish systems were investigated to examine the relationship between the accumulation and their physicochemical processes in soils. The results indicate that the distribution of pharmaceuticals between soil and pore water, as well as their biodegradation, combined to govern the bioavailability of pharmaceuticals to plant uptake. Fourteen out of 15 pharmaceuticals could enter radish tissues in which the accumulation ranged from 2.1 to 14080 ng/g. Comparison of bio-concentration factors (BCFs) on the basis of pharmaceutical concentration in bulk soil vs. in pore water implies that pharmaceuticals present in soil pore water are the major bioavailable fractions to plant uptake. The pore water-based BCFs exhibited a positive linear relationship with log D-ow for the pharmaceuticals with >90% as neutral species in soil pore water, while such relationship was not observed between bulk soil-based BCFs and log D-ow mainly due to sorption by soil. Other than hydrophobicity, the dissociation of ionizable pharmaceuticals in the soil pore water and (or) root cells may lead to the ion-trap effects and thus influence the uptake and translocation process. The large molecular-size pharmaceuticals (e.g., tylosin) manifested a minimum uptake due plausibly to the limited permeability of cell membranes. (C) 2019 Elsevier Ltd. All rights reserved.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据