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Hauptverfasser: Noman, Md Abu, Trevathan-Tackett, Stacey M, Macreadie, Peter I, Connolly, Rod M, Chen, Zhao Liang, He, Ding, Adyel, Tanveer M
Format: Artículo científico
Sprache:en
Veröffentlicht: Environmental pollution (Barking, Essex : 1987) 2026
Schlagworte:
Online-Zugang:https://pubmed.ncbi.nlm.nih.gov/41448335/
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author Noman, Md Abu
Trevathan-Tackett, Stacey M
Macreadie, Peter I
Connolly, Rod M
Chen, Zhao Liang
He, Ding
Adyel, Tanveer M
author_facet Noman, Md Abu
Trevathan-Tackett, Stacey M
Macreadie, Peter I
Connolly, Rod M
Chen, Zhao Liang
He, Ding
Adyel, Tanveer M
Noman, Md Abu
Trevathan-Tackett, Stacey M
Macreadie, Peter I
Connolly, Rod M
Chen, Zhao Liang
He, Ding
Adyel, Tanveer M
collection PubMed - marine biology
contents Unravelling the molecular fingerprint of plastic accumulation on blue carbon sediment. Noman, Md Abu Trevathan-Tackett, Stacey M Macreadie, Peter I Connolly, Rod M Chen, Zhao Liang He, Ding Adyel, Tanveer M Geologic Sediments Plastics Carbon Environmental Monitoring Water Pollutants, Chemical Polyesters Polyethylene Terephthalates A disproportionately large accumulation of plastic waste has turned blue carbon ecosystems (mangrove forests, tidal marshes, and seagrass meadows) into hotspots of plastic pollution. Although our understanding of the effects of plastics on coastal ecosystems has advanced considerably, the underlying effects on blue carbon sediment biogeochemistry are yet to be assessed. Here, we examined the potential organic matter turnover and degradability of conventional plastics, i.e. polyethylene terephthalate (PET) and polypropylene (PP) and biodegradable plastic, i.e. polylactic acid (PLA) in a controlled microcosm experiment containing mangrove sediments. We measured dissolved organic carbon (DOC) leaching, changes in sediment dissolved organic matter (DOM), and the simultaneous greenhouse gas emissions caused by plastics. After 90 days of incubation, low molecular weight PP was visibly degraded on the surface, but high molecular weight PET and PLA were not. The degradation of PP and granular structure of PET led to higher DOC content and number of DOM molecules in sediment compared to that of PLA. Initially, PET contributed higher bio-labile compounds to the sediment, but after 90 days of incubation biologically recalcitrant compounds were more prominent. Despite contributing less DOC and DOM, sediment with PLA emitted higher CO, suggesting that PLA may accelerate the degradation of native organic matter, whereas PP reduced the cumulative emission. In short, both conventional and biodegradable plastics affect sediment biogeochemistry by altering DOC content, DOM composition and turnover. This study provides new insights into the signature of different plastics in blue carbon sediment dynamics.
format Artículo científico
id pubmed_41448335
institution PubMed
language en
publishDate 2026
publisher Environmental pollution (Barking, Essex : 1987)
record_format pubmed
spellingShingle Unravelling the molecular fingerprint of plastic accumulation on blue carbon sediment.
Noman, Md Abu
Trevathan-Tackett, Stacey M
Macreadie, Peter I
Connolly, Rod M
Chen, Zhao Liang
He, Ding
Adyel, Tanveer M
Geologic Sediments
Plastics
Carbon
Environmental Monitoring
Water Pollutants, Chemical
Polyesters
Polyethylene Terephthalates
Unravelling the molecular fingerprint of plastic accumulation on blue carbon sediment. Noman, Md Abu Trevathan-Tackett, Stacey M Macreadie, Peter I Connolly, Rod M Chen, Zhao Liang He, Ding Adyel, Tanveer M Geologic Sediments Plastics Carbon Environmental Monitoring Water Pollutants, Chemical Polyesters Polyethylene Terephthalates A disproportionately large accumulation of plastic waste has turned blue carbon ecosystems (mangrove forests, tidal marshes, and seagrass meadows) into hotspots of plastic pollution. Although our understanding of the effects of plastics on coastal ecosystems has advanced considerably, the underlying effects on blue carbon sediment biogeochemistry are yet to be assessed. Here, we examined the potential organic matter turnover and degradability of conventional plastics, i.e. polyethylene terephthalate (PET) and polypropylene (PP) and biodegradable plastic, i.e. polylactic acid (PLA) in a controlled microcosm experiment containing mangrove sediments. We measured dissolved organic carbon (DOC) leaching, changes in sediment dissolved organic matter (DOM), and the simultaneous greenhouse gas emissions caused by plastics. After 90 days of incubation, low molecular weight PP was visibly degraded on the surface, but high molecular weight PET and PLA were not. The degradation of PP and granular structure of PET led to higher DOC content and number of DOM molecules in sediment compared to that of PLA. Initially, PET contributed higher bio-labile compounds to the sediment, but after 90 days of incubation biologically recalcitrant compounds were more prominent. Despite contributing less DOC and DOM, sediment with PLA emitted higher CO, suggesting that PLA may accelerate the degradation of native organic matter, whereas PP reduced the cumulative emission. In short, both conventional and biodegradable plastics affect sediment biogeochemistry by altering DOC content, DOM composition and turnover. This study provides new insights into the signature of different plastics in blue carbon sediment dynamics.
title Unravelling the molecular fingerprint of plastic accumulation on blue carbon sediment.
topic Geologic Sediments
Plastics
Carbon
Environmental Monitoring
Water Pollutants, Chemical
Polyesters
Polyethylene Terephthalates
url https://pubmed.ncbi.nlm.nih.gov/41448335/