Wang Hong-Ju, Li Qian-Qian, Shen Yu, Gu Ruo-Chen, Sheng Yu, Zhan Xin-Hua
College of Resources and Environmental Sciences, Nanjing Agricultural University, Nanjing 210095, China.
Huan Jing Ke Xue. 2017 Jun 8;38(6):2561-2567. doi: 10.13227/j.hjkx.201612020.
The study of PAHs sorption and bioavailability to different crop roots could help to reveal the environmental behavior of PAHs in the ecosystem and evaluate the ecological risk of PAHs. However, there is little information about the differences in PAHs sorption to different roots and the bioavailability of the sorbed PAHs. In this paper, the experiments were conducted on the sorption/desorption of phenanthrene to soybean and wheat roots under different sorption times and different phenanthrene concentrations. The results showed that the trend of phenanthrene sorption in vivo was first increased and then decreased and finally reached a balance, which was related to the transport delay in vivo; the trend in dead and dried roots was first increased and then reached a balance. The greater specific surface area and the higher fat content, the faster the balance was. Freundlich isotherm was fitted better than Henry isotherm for dead and dried roots, Langmuir isotherm was best fitted in wheat roots. All of the fitted isotherms indicated that the distribution and the surface adsorption could control the phenanthrene sorption. Because of the special binding between living roots and phenanthrene, the fit effect was poor. The phenanthrene sorption capacity of soybean roots was higher than that of wheat, which was related to the high water content, fat content and membrane permeability. The phenanthrene sorbed on the roots was hard to desorb, and the desorption trends were wheat roots> soybean roots; living roots> dried roots> dead roots. The bioavailability of root-sorbed phenanthrene was consistent with the desorption results. Our results could provide data for the assessment of environmental risks of PAHs sorbed onto crop roots.
多环芳烃对不同作物根系的吸附及其生物有效性研究,有助于揭示多环芳烃在生态系统中的环境行为,并评估多环芳烃的生态风险。然而,关于多环芳烃在不同根系上的吸附差异以及吸附态多环芳烃的生物有效性,目前的信息较少。本文开展了菲在不同吸附时间和不同菲浓度下对大豆和小麦根系的吸附/解吸实验。结果表明,菲在活体根系中的吸附趋势为先增加后降低,最终达到平衡,这与体内运输延迟有关;在死根和干根中的趋势为先增加后达到平衡。比表面积越大、脂肪含量越高,达到平衡的速度越快。对于死根和干根,Freundlich等温线的拟合效果优于Henry等温线,Langmuir等温线在小麦根系中拟合效果最佳。所有拟合的等温线均表明,分配作用和表面吸附作用可控制菲的吸附。由于活体根系与菲之间存在特殊的结合作用,拟合效果较差。大豆根系对菲的吸附能力高于小麦根系,这与大豆根系较高的含水量、脂肪含量和膜通透性有关。吸附在根系上的菲难以解吸,解吸趋势为小麦根系>大豆根系;活体根系>干根>死根。根系吸附态菲的生物有效性与解吸结果一致。我们的研究结果可为评估吸附在作物根系上的多环芳烃的环境风险提供数据。