Microplastics alter nitrous oxide production and pathways through affecting microbiome in estuarine sediments.

Increasing microplastics (MPs) pollution in estuaries profoundly impacts microbial ecosystems and biogeochemical processes. Nitrous oxide (N2O), a powerful greenhouse gas, is an important intermediate product of microbial nitrogen cycling. However, how MPs regulate N2O production and its pathways remain poorly understood. Here, impacts of traditional petroleum-based and emerging biodegradable MPs on microbial N2O production and its pathways were studied through dual-isotope (15N-18O) labeling technique and molecular methods. Results indicated that both traditional petroleum-based and emerging biodegradable MPs promoted sedimentary N2O production, whereas pathways varied. Biodegradable polylactic acid (PLA) MPs displayed greater promotion of N2O production than petroleum-based MPs, polyvinyl chloride (PVC) and polyethylene (PE), of which PLA promoted through nitrifier nitrification (NN) and heterotrophic denitrification (HD), PE through nitrifier denitrification and HD, and PVC through NN. By combining the analysis of N2O production rates with sediment chemical and microbiological properties, we demonstrated that the enrichment of nitrifying and denitrifying bacteria, as well as related functional genes directly and/or indirectly increased N2O production primarily by interacting with carbon and nitrogen substrates. Different response of nitrogen cycling microbes to MPs led to the difference in N2O increase pathways, of which nitrifying bacteria significantly enriched in all MPs treatments due to the niches provided by MPs. However, part of denitrifying bacteria significantly enriched in treatments containing PLA and PE MPs, which may serve as organic carbon substrates. This work highlights that the presence of MPs can promote sedimentary N2O production, and the emerging biodegradable MPs represented by PLA may have a greater potential to enhance estuarine N2O emissions and accelerate global climate change.

[Distribution of matrix-bound phosphine in surface sediments of Jinpu Bay].

This work investigated the distribution of matrix-bound phosphine in surface sediments of Jinpu Bay and associated environmental factors in summer, using the gas chromatography combined with a pulsed flame detector (GC-PFPD). It showed that phosphine ubiquitously presented in the sediments of Jinpu Bay. Contents of matrix-bound phosphine varied between 62. 58 and 190. 81 ng.kg-1, with the average value of 114.42 ng.kg-1. In addition, the spatial distribution of matrix-bound phosphine indicated that matrix-bound phosphine in inshore sediments had relatively higher contents than those in offshore sediments. Statistical analysis showed that matrix-bound phosphine significantly related to organic phosphorus and alkaline phosphatase activity ( R = 0. 882, P = 0. 01; R = 0. 819, P =0. 023). However, there were no correlations between matrix-bound phosphine and organic nitrogen, inorganic phosphorus and sediment grain sizes. These results implied that accumulation and distribution of matrix-bound phosphined were mainly affected by the decomposition of organic phosphorus by microorganisms.