Synthetic and natural rubber associated chemicals drive functional and structural changes as well as adaptations to antibiotics in in vitro marine microbiomes.

The leaching of additives from plastics and elastomers (rubbers) has raised concerns due to their potential negative impacts on the environment and the development of antibiotic resistance. In this study, we investigated the effects of chemicals extracted from two types of rubber on microbiomes derived from a benthic sea urchin and two pelagic fish species. Additionally, we examined whether bacterial communities preconditioned with rubber-associated chemicals displayed adaptations to antibiotics. At the highest tested concentrations of chemicals, we observed reduced maximum growth rates and yields, prolonged lag phases, and increased alpha diversity. While the effects on alpha and beta diversity were not always conclusive, several bacterial genera were significantly influenced by chemicals from the two rubber sources. Subsequent exposure of sea urchin microbiomes preconditioned with rubber chemicals to the antibiotic ciprofloxacin resulted in decreased maximum growth rates. This indicates a more sensitive microbiome to ciprofloxacin when preconditioned with rubber chemicals. Although no significant interaction effects between rubber chemicals and ciprofloxacin exposure were observed in bacterial alpha and beta diversity, we observed log-fold changes in two bacterial genera in response to ciprofloxacin exposure. These findings highlight the structural and functional alterations in microbiomes originating from various marine species when exposed to rubber-associated chemicals and underscore the potential risks posed to marine life.

Organic chemicals associated with rubber are more toxic to marine algae and bacteria than those of thermoplastics.

The current study investigated the chemical complexity of fifty plastic (36) and elastomer/rubber (14) methanol extracts from consumer products, focusing on the association with toxicity in two screening assays (bacteria luminescence and marine microalgae). The chemical composition varied considerably between the products and polymers. The most complex sample (car tire rubber) contained 2456 chemical features and the least complex (disposable water bottle) only 39 features, with a median of 386 features across all products. Individual extract toxicity also varied significantly across the products and polymers, with the two toxicity assays showing comparable results in terms of defining low and high toxicity extracts, and correlation between medium toxicity extracts. Chemical complexity and abundance both correlated with toxicity in both assays. However, there were strong differences in toxicity between plastic and elastomer extracts. Overall, 86-93 % of the 14 elastomer extracts and only 33-36 % of other polymer extracts (n = 36) were more toxic than the median. A range of compounds were tentatively identified across the sample set, with several concerning compounds being identified, mostly in the elastomers. While the current focus on plastic chemicals is towards thermoplastics, we show that elastomers may be of more concern from an environmental and human health perspective.

Non-target and suspect screening reveal complex pattern of contamination in Arctic marine zooplankton.

Although increasing, there is still limited knowledge of the presence of 'contaminants of emerging concern' in Arctic marine biota, particularly in lower trophic species. In the present study, we have applied a novel pipeline to investigate the presence of contaminants in a variety of benthic and pelagic low-trophic organisms: amphipods, copepods, arrow worms and krill. Samples collected in Kongsfjorden in Svalbard in 2018 were subject to extraction and two-dimensional gas chromatography coupled to high-resolution mass spectrometry (GC×GC-HRMS). Tentatively identified compounds included plastic additives, antioxidants, antimicrobials, flame retardants, precursors, production solvents and chemicals, insecticides, and pharmaceuticals. Both legacy contaminants (PAHs, PCBs, PBDEs, hexachlorobenzene) as well as novel and emerging contaminants (triclosan, bisphenol A, and ibuprofen) were quantified in several species using target analysis by GC-MS/MS. The significance of these discoveries is discussed considering the potential for detrimental effects caused by these chemicals, as well as suggested local and distant sources of the components to the Arctic environment.