Sibo Zhang, Meijuan Yang, Xinghui Xia, Qinyuan Gu, Qun Gao, Junfeng Wang, Shaoda Liu, Xiaokang Li, Yingjie Li, William H. McDowell, Zhifeng Yang
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引用次数: 0
Abstract
Nitrous oxide (N2O) reductase, the sole natural microbial sink for N2O, exists in two microbial clades: nosZI and nosZII. Although previous studies have explored inter-clade ecological differentiation, the intra-clade variations and their implications for N2O dynamics remain understudied. This study investigated both inter- and intra-clade ecological differentiation among N2O reducers, the drivers influencing these patterns, and their effects on N2O emissions across continental-scale river systems. The results showed that both nosZI and nosZII community turnovers were associated with similar key environmental factors, particularly total phosphorus (TP), but these variables explained a larger proportion of variation in the nosZI community. The influence of mean annual temperature (MAT) on community composition increased for more widespread N2O-reducing taxa. We identified distinct ecological clusters within each clade of N2O reducers and observed identical ecological clustering patterns across both clades. These clusters were primarily characterized by distinct MAT regimes, coarse sediment texture as well as low TP levels, and high abundance of N2O producers, with MAT-related clusters constituting predominant proportions. Intra-clade ecological differentiation was a crucial predictor of N2O flux and reduction efficiency. Although different ecological clusters showed varying or even contrasting associations with N2O dynamics, the shared ecological clusters across clades exhibited similar trends. Low-MAT clusters in both the nosZI and nosZII communities were negatively correlated with denitrification-normalized N2O flux and the N2O:(N2O + N2) ratio, whereas high-MAT clusters showed positive correlations. This contrasting pattern likely stems from low-MAT clusters being better adapted to eutrophic conditions and their more frequent co-occurrence with N2O-producing genes. These findings advance our understanding of the distribution and ecological functions of N2O reducers in natural ecosystems, suggesting that warming rivers may have decreased N2O reduction efficiency and thereby amplify temperature-driven emissions.
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.