Elias D A, Krumholz L R, Wong D, Long P E, Suflita J M
Institute for Energy and the Environment and the Department of Botany and Microbiology, University of Oklahoma, Norman, OK 73019, USA.
Microb Ecol. 2003 Jul;46(1):83-91. doi: 10.1007/s00248-002-1060-x. Epub 2003 May 21.
A characterization of the Shiprock, NM, uranium mill tailing site focused on the geochemical and microbiological factors governing in-situ uranium-redox reactions. Groundwater and aqueous extracts of sediment samples contained a wide concentration range of sulfate, nitrate, and U(VI) with median values of 21.2 mM, 16.1 micro M, and 2.7 micro M, respectively. Iron(III) was not detected in groundwater, but a median value of 0.3 mM in sediment extracts was measured. Bacterial diversity down gradient from the disposal pile reflected the predominant geochemistry with relatively high numbers of sulfate- and nitrate-reducing microorganisms, and smaller numbers of acetogenic, methanogenic, nitrate-dependent Fe(II)-oxidizing, Fe(III)-reducing, and sulfide-oxidizing bacteria. In aquifer slurry incubations, nitrate reduction was always preferred and had a negative impact on sulfate-, Fe(III)-, and U-reduction rates. We also found that sulfate-reduction rates decreased sharply in the presence of clay, while Fe(III)-reduction increased with no clear impact on U reduction. In the absence of clay, iron and sulfate reduction correlated with concentrations of Fe(III) and sulfate, respectively. Rates of U(VI) loss did not correlate with the concentration of any electron acceptor. With the exception of Fe(III), electron donor amendment was largely unsuccessful in stimulating electron acceptor loss over a 2-week incubation period, suggesting that endogenous forms of organic matter were sufficient to support microbial activity. Our findings suggest that efforts to accelerate biological U reduction should initially focus on stimulating nitrate removal.
对新墨西哥州希普罗克铀矿尾矿场的特征进行了研究,重点关注控制原位铀氧化还原反应的地球化学和微生物因素。沉积物样本的地下水和水提取物中硫酸盐、硝酸盐和U(VI)的浓度范围很广,中位数分别为21.2 mM、16.1 μM和2.7 μM。地下水中未检测到铁(III),但沉积物提取物中的中位数为0.3 mM。从处置堆向下的细菌多样性梯度反映了主要的地球化学特征,硫酸盐还原菌和硝酸盐还原菌数量相对较多,而产乙酸菌、产甲烷菌、硝酸盐依赖的Fe(II)氧化菌、Fe(III)还原菌和硫化物氧化菌数量较少。在含水层泥浆培养中,硝酸盐还原总是优先发生,并且对硫酸盐、Fe(III)和U的还原速率有负面影响。我们还发现,在有粘土的情况下,硫酸盐还原速率急剧下降,而Fe(III)还原增加,对U还原没有明显影响。在没有粘土的情况下,铁还原和硫酸盐还原分别与Fe(III)和硫酸盐的浓度相关。U(VI)损失速率与任何电子受体的浓度均无相关性。除Fe(III)外,在为期2周的培养期内,添加电子供体在很大程度上未能刺激电子受体的损失,这表明内源性有机物质足以支持微生物活动。我们的研究结果表明,加速生物还原铀的努力应首先集中在刺激硝酸盐去除上。