生物地球化学循环
全球变暖
微观世界
环境科学
反硝化细菌
氮气循环
自行车
生态系统
缺氧水域
全球变暖对海洋的影响
反硝化
生态学
环境化学
气候变化
生物地球化学
河口
营养循环
海洋生态系统
污染
硝酸盐
缺氧(环境)
化学
沉积物
中观
硝化作用
磷石膏
全球变化
营养污染
氮气
微生物种群生物学
海洋学
生物量(生态学)
多毛类
作者
Cheng Chen,Y. S. Zhang,Guoyu Yin,Dongyao Sun,Ye Li,Lijun Hou,Min Liu
标识
DOI:10.1021/acs.est.5c08930
摘要
Global warming and microplastics (MPs) pollution are emerging stressors that threaten coastal ecosystems, yet their combined impacts on biogeochemical cycles remain poorly resolved. Here, we integrated a factorial microcosm experiment with stable isotope tracing and molecular techniques to disentangle how warming and MPs jointly regulate nitrogen (N) cycling in coastal sediments. We demonstrate that warming and MPs interacted nonadditively to reshape nitrification, denitrification, and associated nitrous oxide (N2O) production dynamics. Warming reversed the stimulatory effect of polyethylene (PE) on nitrification, turning it inhibitory, and amplified the suppressive impact of poly(butylene adipate-co-terephthalate) (PBAT), primarily through synergistic intensification of anoxic stress. In contrast, warming strengthened PE-driven stimulation of denitrification and mitigated PBAT-induced inhibition, likely due to the selective enrichment of nirS- and nosZ-harboring denitrifiers. Moreover, warming overturned the stimulatory effects of both PE and PBAT on N2O production, shifting toward inhibition through nitrifier denitrification, as substantiated by dual-isotope (15N–18O) tracing and genomic evidence. Collectively, these findings provide novel mechanistic insights into how warming interacts with MPs to reconfigure sedimentary N cycling, with broad implications for predicting the responses and evolution of coastal ecosystems under accelerating global change.
科研通智能强力驱动
Strongly Powered by AbleSci AI