溶解有机碳
微塑料
化学
微生物种群生物学
环境化学
生物降解
低密度聚乙烯
变形菌纲
聚合物
有机质
聚乙烯
沉积物
碳纤维
戊酸盐
可生物降解聚合物
微生物降解
食品科学
基因组
傅里叶变换红外光谱
作者
Manman Cao,Feng Wang,Fei Wang,Haodong Huang,Shuai Ma,Junhong Li,Na Xiao,Ruiyi Xie,Ke Sun
标识
DOI:10.1021/acs.est.6c10516
摘要
Abstract Biodegradable polymers are promoted as alternatives to conventional plastics, but their effects on sediment dissolved organic matter (DOM) and microbial communities remain unclear. Here, we estimated impacts of two nonbiodegradable (low-density polyethylene (LDPE) and poly(ethylene terephthalate) (PET)) and two biodegradable (polylactide (PLA) and poly(butylene succinate) (PBS)) polymers on DOM composition and microbial functional profiles using Fourier transform ion cyclotron resonance mass spectrometry (FT-ICR MS) and metagenomic sequencing. The tested nonbiodegradable polymers shifted DOM toward recalcitrance. In contrast, biodegradable polymers exhibited divergent trajectories: PLA shifted from labile at day 30 to recalcitrant by day 60, whereas PBS showed the opposite trend toward instability. Microbial communities shifted from high-abundance Deltaproteobacteria (∼12%) at day 30 to Alphaproteobacteria (∼16%) and Actinomycetia (∼15%) at day 60. Glycolysis genes were less abundant under LDPE and PET, while fatty acid β-oxidation genes were enriched under LDPE, PET, and PLA. Spearman correlation and Mantel tests revealed that MP-driven DOM changes were associated with microbial community restructuring and bacterial diversity. This study highlights that biodegradable polymers cannot be assumed to have negligible sediment ecological impacts simply because of their degradable classification.
科研通智能强力驱动
Strongly Powered by AbleSci AI