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Field-scale 13C-labeling of phospholipid fatty acids (PLFA) and dissolved inorganic carbon: tracing acetate assimilation and mineralization in a petroleum hydrocarbon-contaminated aquifer

机译:现场规模的13C标记磷脂脂肪酸(PLFA)和溶解的无机碳:在石油烃污染的含水层中追踪乙酸同化和矿化作用

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摘要

This study was conducted to determine the feasibility of labeling phospholipid-derived fatty acids (PLFA) of an active microbial population with a 13C-labeled organic substrate in the denitrifying zone of a petroleum hydrocarbon-contaminated aquifer during a single-well push-pull test. Anoxic test solution was prepared from 500 l of groundwater with addition of 0.5 mM Br− as a conservative tracer, 0.5 mM NO3−, and 0.25 mM [2-13C]acetate. At 4, 23 and 46 h after injection, 1000 l of test solution/groundwater mixture were sequentially extracted. During injection and extraction phases we measured Br−, NO3− and acetate concentrations, characterized the microbial community structure by PLFA and fluorescent in situ hybridization (FISH) analyses, and determined 13C/12C ratios in dissolved inorganic carbon (DIC) and PLFA. Computed first-order rate coefficients were 0.63±0.08 day−1 for NO3− and 0.70±0.05 day−1 for acetate consumption. Significant 13C incorporation in DIC and PLFA was detected as early as 4 h after injection. At 46 h we measured δ13C values of up to 5614‰ in certain PLFA (especially monounsaturated fatty acids), and up to 59.8‰ in extracted DIC. Profiles of enriched PLFA and FISH analysis suggested the presence of active denitrifiers. Our results demonstrate the applicability of 13C labeling of PLFA and DIC in combination with FISH to link microbial structure and activities at the field scale during a push-pull test
机译:进行这项研究是为了确定在单井推挽试验中,用石油烃污染的含水层反硝化区中13 C标记的有机底物标记活性微生物种群的磷脂源脂肪酸(PLFA)的可行性。 。由500升地下水,添加0.5 mM Br-作为保守示踪剂,0.5 mM NO3-和0.25 mM [2-13C]乙酸盐制备缺氧测试溶液。注入后第4、23和46小时,依次提取1000升测试溶液/地下水混合物。在注入和萃取阶段,我们测量了Br-,NO3-和乙酸盐的浓度,通过PLFA和荧光原位杂交(FISH)分析表征了微生物群落结构,并确定了溶解无机碳(DIC)和PLFA中的13C / 12C比。对于NO3-,计算的一级速率系数为0.63±0.08天-1,对于乙酸盐消耗为0.70±0.05天-1。最早在注射后4小时就检测到DIC和PLFA中有大量13C掺入。在46 h时,我们在某些PLFA(尤其是单不饱和脂肪酸)中测得的δ13C值高达5614‰,而在DIC中测得的δ13C值则高达59.8‰。丰富的PLFA和FISH分析结果表明存在活性反硝化剂。我们的结果证明了PLFA和DIC的13C标记与FISH结合在推挽试验过程中在田间规模上链接微生物结构和活性的适用性

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