Hall J A, Mailloux B J, Onstott T C, Scheibe T D, Fuller M E, Dong H, DeFlaun M F
Geophysical Laboratory, Carnegie Institute Washington, 5251 Broad Branch Rd., N.W, Washington, DC 20015, USA.
J Contam Hydrol. 2005 Feb;76(3-4):295-314. doi: 10.1016/j.jconhyd.2004.11.003. Epub 2005 Jan 11.
Twenty-eight bacterial and Br transport experiments were performed in the field to determine the effects of physical and chemical heterogeneity of the aquifer sediment. The experiments were performed using groundwater from two field locations to examine the effects of groundwater chemistry on transport. Groundwater was extracted from multilevel samplers and pumped through 7-cm-long columns of intact sediment or repacked sieved and coated or uncoated sediment from the underlying aquifer. Two bacterial strains, Comamonas sp. DA001 and Paenibacillus polymyxa FER-02, were injected along with Br into the influent end of columns to examine the effect of cell morphology and cell surface properties on bacterial transport. The effects of column sediment grain size and mineral coatings coupled with groundwater geochemistry were also investigated. Significant irreversible attachment of DA001 was observed in the Fe oxyhydroxide-coated columns, but only in the suboxic groundwater where the concentrations of dissolved organic carbon (DOC) were ca. 1 ppm. In the oxic groundwater where DOC was ca. 8 ppm, little attachment of DA001 to the Fe oxyhydroxide-coated columns was observed. This indicates that DOC can significantly reduce bacterial attachment due electrostatic interactions. The larger and more negatively charged FER-02 displayed increasing attachment with decreasing grain size regardless of DOC concentration, and modeling of FER-02 attachment revealed that the presence of Fe and Al coatings on the sediment also promoted attachment. Finally, the presence of Al coatings and Al containing minerals appeared to significantly retard the Br tracer regardless of the concentration of DOC. These findings suggest that DOC in shallow oxic groundwater aquifers can significantly enhance the transport of bacteria by reducing attachment to Fe, Mn and Al oxyhydroxides. This effect appears to be profound for weakly and strongly charged hydrophilic bacteria and may contribute to differences in observations between laboratory experiments versus field-scale investigations particularly if the groundwater pH remains subneutral and Fe oxyhydroxide phases exist. These observation validate the novel approach taken in the experiments outlined here of performing laboratory-scale experiments on site to facilitate the use of fresh groundwater and thus be more representative of in situ groundwater conditions.
为确定含水层沉积物物理和化学非均质性的影响,在野外进行了28次细菌和溴运移实验。实验使用了来自两个野外地点的地下水,以研究地下水化学性质对运移的影响。从多级采样器中抽取地下水,然后将其泵入由7厘米长的原状沉积物柱,或由下层含水层筛分、涂覆或未涂覆的沉积物重新装填而成的柱中。将两种细菌菌株,即食酸丛毛单胞菌DA001和多粘类芽孢杆菌FER-02与溴一起注入柱的进水端,以研究细胞形态和细胞表面性质对细菌运移的影响。同时还研究了柱沉积物粒度和矿物涂层与地下水地球化学的综合影响。在氢氧化铁涂层柱中观察到DA001有显著的不可逆附着,但仅在溶解有机碳(DOC)浓度约为1 ppm的缺氧地下水中。在DOC约为8 ppm的有氧地下水中,未观察到DA001在氢氧化铁涂层柱上有明显附着。这表明DOC可通过静电相互作用显著减少细菌附着。无论DOC浓度如何,更大且带更多负电荷的FER-02随着粒度减小附着增加,FER-02附着的模型显示沉积物上铁和铝涂层的存在也促进了附着。最后,无论DOC浓度如何,铝涂层和含铝矿物的存在似乎显著阻滞了溴示踪剂。这些发现表明,浅层有氧地下水含水层中的DOC可通过减少与铁、锰和氢氧化铝的附着,显著增强细菌的运移。这种效应对于带弱电荷和强电荷的亲水性细菌似乎尤为显著,可能导致实验室实验与现场规模调查结果的差异,特别是当地下水电导率保持亚中性且存在氢氧化铁相时。这些观察结果验证了此处概述的实验所采用的新方法,即在现场进行实验室规模的实验,以便使用新鲜地下水,从而更能代表原位地下水条件。