同位素和微生物组分析表明,排干泥炭地森林土壤中控制N2O通量的n循环过程的多样性

Mohit Masta, Sharvari S. Gadegaonkar, Holar Sepp, Mikk Espenberg, J. Pärn, K. Kirsimäe, Ü. Mander
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引用次数: 0

摘要

一氧化二氮(N2O)是一种主要的温室气体,其在大气中的存在不断增加。因此,了解其生产和消费机制非常重要。2020年夏季,我们利用硝酸钾15N 98%原子(Sigma Aldrich)和氯化铵15N 98%原子(Sigma Aldrich)在不同水分条件下的重氮示踪剂进行了实验室实验,以深入了解N2O的产生机制及其对土壤水分的依赖。我们将示踪剂应用于泥炭样品(Kärevere,爱沙尼亚),放置在36个塑料桶(12个对照,12个硝酸盐处理和12个氨处理)中(半径-10厘米,高度-20厘米),土壤高度为10厘米,顶部空间为10厘米用于气体收集。我们在所有水桶上安装了氧气传感器、地下水位指示器和温度传感器。我们重点研究了物理条件(土壤氧、温度、地下水位和土壤湿度)、气体(N2O)排放数据、土壤化学、气体同位素15N、土壤同位素和土壤微生物学,以全面了解N2O气体产生的过程。在氨处理下,排放量增加了十倍以上,这可能是由于氮循环的多个过程在起作用。当氧条件由缺氧状态(Omg/L=0)转变为亚氧状态(Omg/L=0.5–6)时,N2O排放量增加,当氧状态(Omg/L>6)时,N2O排放量减少。此外,在硝酸盐处理期间,我们发现负的位点偏好和18O值表明硝化-反硝化作用。在氨处理下,我们记录到阴性和高阳性位点偏好值,表明存在多种生产机制。这是意料之中的,因为氨触发了氮循环中的多个过程。在一些样品中,我们观察到与N2O产生样品相比,N2O消耗在场地偏好上几乎没有变化。这表明一些细菌反硝化作用伴随着普遍的硝化反硝化作用。我们还观察到,在两种处理下,重氧随位点偏好的增加而增加。这表明N2O的减少(Ostrom等,2007)作为氧化还原支持15N和18O富集。在这些实验室实验之后,我们在爱沙尼亚Agali的一个排水泥炭地森林中进行了同样的大规模实验。在本次实验中,我们通过实验排水和驱水建立了1m2的三角形中生态系统,以实现不同的氧气条件。n循环控制基因qPCR分析的初步结果支持氨氧化和反硝化作为N2O来源的优势。
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Isotope and microbiome analysis indicates variety of N-cycle processes controlling N2O fluxes in a drained peatland forest soil

Nitrous oxide (N2O) is a major greenhouse gas whose presence in atmosphere is continuously increasing. Hence it’s important to understand its production and consumption mechanisms. During the summer of 2020, we conducted lab experiments using heavy nitrogen tracers of Potassium Nitrate 15N 98% atom (Sigma Aldrich) and Ammonium Chloride 15N 98% atom (Sigma Aldrich) under different moisture conditions to get an insight into N2O production mechanisms and on their dependence on soil moisture. We applied the tracer to peat samples (Kärevere, Estonia) placed in 36 (12 control, 12 nitrate treatment & 12 ammonia treatment) plastic buckets (radius-10cm, height-20cm) with soil height of 10 cm and a 10 cm head space left for gas collection. We installed oxygen sensors, water table indicators and temperature sensors on all buckets. We focused on studying physical conditions (soil oxygen, temperature, water table and soil moisture), gas (N2O) emission data, soil chemistry, gas isotope 15N, soil isotope and soil microbiology to get a complete picture of the processes involved in production of N2O gas. Under the ammonia treatment, emissions increased more than ten-fold which could be due to multiple processes of the nitrogen cycle in play. N2O emissions increased as the oxygen conditions shifted from anoxic (Omg/L=0) to sub-oxic (Omg/L=0.5–6) and then decreased as oxygen conditions reached the oxic (Omg/L>6) state. Furthermore, we witnessed negative site preference and 18O values during the nitrate treatment indicating nitrifier-denitrification. Under the ammonia treatment, we recorded both negative as well as high positive site preference values indicating presence of multiple production mechanisms. This was expected as ammonia triggers multiple processes in the nitrogen cycle. In some samples, we observed N2O consumption with little change in site preference as compared to the N2O producing samples. This indicates some bacterial-denitrification along with the prevailing nitrifier-denitrification. We also observed that under both treatments, heavy oxygen increased with increasing site preference. This indicates reduction of N2O (Ostrom et al, 2007) as redox supports 15N and 18O enrichments. After these lab experiments, we conducted the same experiment at a large scale in a drained peatland forest in Agali, Estonia. In this experiment, we established 1m2 triangle-shape mesocosms using experimental draining and flooding to achieve varying oxygen conditions. Preliminary results of qPCR analysis of N-cycle control genes support the domination of ammonia oxidation and denitrification as sources of N2O.

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