Dai Jun-Shuai, Zuo Xiao-Hu, Wang Ming-Xia, Yao Yan-Hong, Zhou Zhi-Feng
College of Resources and Environment, Southwest University, Chongqing 400715, China.
Huan Jing Ke Xue. 2018 Jan 8;39(1):422-429. doi: 10.13227/j.hjkx.201706267.
The degradation of soil polycyclic aromatic hydrocarbons (PAHs) under denitrification is one of the most important pathways for anaerobic PAH elimination, but little is known about the effect of nitrate (the terminal electron acceptor for denitrification) on soil denitrification activity and PAH degradation under anaerobic conditions. In this study, the effect of nitrate on soil anthracene anaerobic degradation and denitrification activity was investigated through an anaerobic microcosm experiment. Two groups of treatments without (N) and with (N) nitrate (30 mg·kg) amendment were conducted. Each group contained three treatments with different anthracene concentrations (0, 15, and 30 mg·kg, denoted as A, A, and A, respectively). Therefore, a total of six treatments (NA, NA, NA, NA, NA, and NA) were incubated in darkness at 25℃ for 45 days, and the production rates of NO and CO, abundances of denitrification related genes (:periplasmic nitrate reductase gene; :copper-containing nitrite reductase gene; and :-nitrite reductase gene), and soil anthracene content were measured at 3, 7, 14, and 45 days. The results indicated that the intensive denitrification enzyme activity in each treatment was only detected at day 3, which could be significantly enhanced by both nitrate and anthracene amendments. Subsequently, a sharp decline of denitrification enzyme activity was observed in each treatment, while anthracene showed an obvious inhibition of soil denitrification enzyme activity. The result of a two-way ANOVA also indicated that nitrate, anthracene, and their interactions had significant effects on soil denitrification enzyme activity. The result of a quantitative-PCR indicated that, during the incubation, the abundances of and exhibited an increasing tendency, but the abundance of was relatively constant compared with its former counterparts. The final removal rate of anthracene under anaerobic soil environment was in the range of 33.83%-55.01%, and neither the final removal rate nor the degradation rate of anthracene could be significantly affected by nitrate amendment during incubation. The anthracene degradation rates in the higher anthracene containing treatments (NA and NA) were significantly higher than those in the lower anthracene containing treatments (NA and NA). In summary, nitrate amendments had no effect on soil anthracene anaerobic degradation but could significantly affect soil denitrification enzyme activity and the abundance of denitrification related and genes.
反硝化作用下土壤多环芳烃(PAHs)的降解是厌氧条件下PAHs去除的最重要途径之一,但关于硝酸盐(反硝化作用的终端电子受体)对厌氧条件下土壤反硝化活性和PAH降解的影响知之甚少。在本研究中,通过厌氧微观试验研究了硝酸盐对土壤蒽厌氧降解和反硝化活性的影响。进行了两组处理,一组不添加硝酸盐(N),另一组添加硝酸盐(30 mg·kg,记为N)。每组包含三种不同蒽浓度(0、15和30 mg·kg,分别记为A0、A15和A30)的处理。因此,总共六种处理(NA0、NA15、NA30、NA0、NA15和NA30)在25℃黑暗条件下培养45天,并在第3、7、14和45天测量NO和CO2的产生速率、反硝化相关基因(napA:周质硝酸盐还原酶基因;nirK:含铜亚硝酸盐还原酶基因;nirS:细胞色素cd1亚硝酸盐还原酶基因)的丰度以及土壤蒽含量。结果表明,各处理中强烈的反硝化酶活性仅在第3天检测到,硝酸盐和蒽添加均可显著增强该活性。随后,各处理中反硝化酶活性均急剧下降,而蒽对土壤反硝化酶活性表现出明显的抑制作用。双向方差分析结果还表明,硝酸盐、蒽及其相互作用对土壤反硝化酶活性有显著影响。定量PCR结果表明,在培养过程中,napA和nirK的丰度呈上升趋势,但nirS的丰度与其之前相比相对稳定。厌氧土壤环境下蒽的最终去除率在33.83% - 55.01%范围内,培养过程中硝酸盐添加对蒽的最终去除率和降解率均无显著影响。高蒽含量处理(NA15和NA30)中的蒽降解率显著高于低蒽含量处理(NA0和NA0)。总之,硝酸盐添加对土壤蒽厌氧降解无影响,但可显著影响土壤反硝化酶活性以及反硝化相关napA和nirK基因的丰度。