Oded Bergman, Katey Walter Anthony, E. Eliani-Russak, Orit Sivan
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Winter methanotrophy was negligible within and above the methanogenic zone, leading to elevated CH<sub>4</sub> production and emission to the atmosphere. This is likely due to reduced microbial methanotrophic activity associated with lower temperatures and nitrogen availability. During summer, strong aerobic methanotrophy near the soil surface reduced CH<sub>4</sub> emissions. Nitrate/nitrite-mediated anaerobic oxidation of methane (AOM) by both archaea (ANME-2d clade) and bacteria (NC10 phylum) occurred at and above the anoxic methanogenic zone, further offsetting CH<sub>4</sub> production. In contrast to CH4 production potentials, which were higher in surface soils in winter compared to summer, we observed higher N<sub>2</sub>O production potentials in summer compared to winter. Nitrous oxide concentrations peaked at 10 cm (7.2 μM) and 105 cm (6.7 μM) and were associated with denitrification; nitrogen-mediated AOM by <i>Methanoperedens</i> (ANME2d). 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引用次数: 0
摘要
大量的碳和氮库不成比例地集中在北极Yedoma永久冻土的更新世泥沙沉积物中。解冻后,这些土壤发生微生物矿化,释放出包括二氧化碳(CO2)、甲烷(CH4)和一氧化二氮(N2O)在内的温室气体(ghg)。在这里,我们将地球化学数据与微生物功能和群落动态相结合,这些数据来自于阿拉斯加内陆水不饱和盐田高地的深层(7米)talik土壤钻孔。我们的研究结果揭示了整个谈话中微生物功能,群落组成和多样性的显著原位季节性变化。甲烷的生成在深海中常年持续。在产甲烷区内外,冬季产甲烷作用可忽略不计,导致CH4的产生和向大气排放增加。这可能是由于较低的温度和氮的可用性降低了微生物的甲烷营养活性。夏季,土壤表层强的好氧甲烷化作用减少了CH4的排放。古生菌(ANME-2d分支)和细菌(NC10门)通过硝酸盐/亚硝酸盐介导的甲烷厌氧氧化(AOM)发生在缺氧产甲烷区及其以上,进一步抵消了CH4的产生。表层土壤CH4生产潜力冬季高于夏季,而N2O生产潜力夏季高于冬季。氧化亚氮浓度在10 cm (7.2 μM)和105 cm (6.7 μM)处达到峰值,与反硝化作用有关;氮介导的methanopenens (ANME2d) AOM。仅在夏季和土壤顶部1 m内,氮相关基因(narG、norB、amoA、Annamox和Feammox)的高表达表明氧化还原动态活跃,可能为AOM提供氮种。由于气候变化导致未来夏季变长,土壤变暖,夏季潜在的N2O产量可能意味着yedoma高地温室气体净排放量增加。
Nitrogen Redox Controls on Greenhouse Gas Production in Yedoma Taliks
Large carbon and nitrogen pools are disproportionately concentrated in the icy, Pleistocene-aged silt deposits of Arctic Yedoma permafrost. Upon thaw, these undergo microbial mineralization, releasing greenhouse gases (GHGs) including carbon dioxide (CO2), methane (CH4), and nitrous oxide (N2O). Here, we present combined geochemical data with microbial function and community dynamics from deep (7-m) talik soil boreholes in water-unsaturated yedoma upland in interior Alaska. Our results reveal significant in situ seasonal shifts in microbial function, community composition, and diversity throughout the talik. Methanogenesis persisted in the deep talik year-round. Winter methanotrophy was negligible within and above the methanogenic zone, leading to elevated CH4 production and emission to the atmosphere. This is likely due to reduced microbial methanotrophic activity associated with lower temperatures and nitrogen availability. During summer, strong aerobic methanotrophy near the soil surface reduced CH4 emissions. Nitrate/nitrite-mediated anaerobic oxidation of methane (AOM) by both archaea (ANME-2d clade) and bacteria (NC10 phylum) occurred at and above the anoxic methanogenic zone, further offsetting CH4 production. In contrast to CH4 production potentials, which were higher in surface soils in winter compared to summer, we observed higher N2O production potentials in summer compared to winter. Nitrous oxide concentrations peaked at 10 cm (7.2 μM) and 105 cm (6.7 μM) and were associated with denitrification; nitrogen-mediated AOM by Methanoperedens (ANME2d). In the summer only and within the top 1 m of soil, high expression of nitrogen-related genes (narG, norB, amoA, Annamox, and Feammox) indicated active redox dynamics, potentially providing nitrogen species for AOM. The potential N2O production in summer may imply higher net GHG emissions from yedoma uplands as climate change leads to longer summers and warmer soils in the future.
期刊介绍:
Global Change Biology is an environmental change journal committed to shaping the future and addressing the world's most pressing challenges, including sustainability, climate change, environmental protection, food and water safety, and global health.
Dedicated to fostering a profound understanding of the impacts of global change on biological systems and offering innovative solutions, the journal publishes a diverse range of content, including primary research articles, technical advances, research reviews, reports, opinions, perspectives, commentaries, and letters. Starting with the 2024 volume, Global Change Biology will transition to an online-only format, enhancing accessibility and contributing to the evolution of scholarly communication.