Zhiguo Pei

The rhizobium-legume symbiosis plays a vital role in the global nitrogen cycle. Although microplastics have been shown to affect this symbiotic system, the accumulation and impacts of nanoplastics (NPs) in rhizobia and their root nodules remain poorly understood, particularly regarding the interactive effects of NPs of different sizes on symbiotic nitrogen fixation. This study demonstrated that polystyrene (PS) NPs exhibited a significant size difference effect on rhizobia and their symbiotic nitrogen-fixing association with soybean (Glycine max). We found that both rhizobia and soybean nodules efficiently internalized PS NPs, with differently sized NPs showing mutual enhancement during the cellular uptake of rhizobia. 100 mg/kg of 20 nm PS NPs severely disrupted the symbiotic nitrogen fixation, reducing nitrogenase activity by 51.3% in single exposures and 28.6% in combined exposure to 200 nm PS NPs. This observed disruption caused by 20 nm PS NPs was associated with suppressed nodule formation (26.0% reduction in number, 50.4% decrease in fresh biomass), diminished leghemoglobin content (64.9% reduction), impaired nutrient acquisition (26.5% decrease in nodule Mo content), reduced rhizobia infection efficiency, impaired plant growth, and modified expression of nodulation- and nitrogen-fixation-related genes. These findings revealed that small-sized PS NPs posed a substantial threat to the rhizobium-legume symbiosis, underscoring the ecological risks of NP pollution in agricultural systems.

The increasing prevalence of organophosphate esters (OPEs) in remote polar ecosystems has raised significant concerns; yet the bioaccumulation and trophic transfer dynamics of these compounds in polar regions remain poorly understood. This study investigated the occurrence and distribution of OPEs in soil, vegetation, marine sediment, and biota from Svalbard, Arctic. Σ₁₀OPEs ranged from 1.12 to 236 ng/g dry weight (dw) and 1.96 to 255 ng/g dw in the Arctic terrestrial and benthic marine matrices, respectively. Triethyl phosphate (TEP), tris(1-chloro-2-propyl) phosphate (TCIPP), tris(2-chloroethyl) phosphate (TCEP), and tri-(2-butoxyethyl) phosphate (TBOEP) were the dominant congeners across all samples. OPEs exhibited bioaccumulation within the soil-vegetation system of the terrestrial environment, while significant trophic dilution occurred in the benthic marine food web. Interestingly, parabolic correlations were observed between log octanol-water partition coefficients (log K_OW) and log-transformed bioconcentration factors (BCFs) in the terrestrial environment, as well as between log K_OW and trophic magnification factors (TMFs) in the benthic marine food web, suggesting that congeners with moderate lipophilicity exhibit the highest potential for bioaccumulation. This study presents the first comprehensive assessment of the bioaccumulation and trophic transfer of OPEs in the Arctic ecosystem, providing critical insights into the environmental behaviors of OPEs in polar regions.

The presence of polyhalogenated carbazoles (PHCZs), which are emerging as dioxin-like contaminants, in remote polar regions has not been reported. This study investigated 11 target PHCZs (Σ₁₁PHCZs) and 25 unknown PHCZs (Σ₂₅UNPs) in soil and sediment samples collected from Ny-Ålesund in the Arctic. The findings revealed that Σ₁₁PHCZs concentrations reached 165.6 ng/g dry weight (dw), with 3,6-dichlorocarbazole and 3-chlorocarbazole being the predominant congeners. The Σ₂₅UNPs concentrations ranged from 1.4 to 92.4 ng/g dw (median: 17.0 ng/g dw), primarily comprising a 1,3,6,8-tetrabromocarbazole isomer. The sediment contained ∼6 times more Σ₂₅UNPs than Σ₁₁PHCZs. Long-range atmospheric transport, oceanic transport, and human activity can potentially affect soils and sediments concurrently. For the first time, halogen substitution patterns in PHCZs, including ClI, ClI₂, and ClI₃, were detected in soil and sediment. Using the toxic equivalent (TEQ) approach, the potential toxic effects linked to the target PHCZ levels were assessed. The TEQ^PHCZs in Arctic soils and sediments indicated low risk, ranging from 8.0 × 10^-3 to 17 pg TEQ/g dw (median: 2.8 pg TEQ/g dw) and 0.1 to 0.4 pg TEQ/g dw (median: 0.3 pg TEQ/g dw), respectively. This study marks the first report on the occurrence, composition, sources, and potential risks posed by PHCZs in the Arctic region.

The pervasive contamination of novel brominated flame retardants (NBFRs) in remote polar ecosystems has attracted great attention in recent research. However, understanding regarding the trophic transfer behavior of NBFRs in the Arctic and Antarctic marine food webs is limited. In this study, we examined the occurrence and trophodynamics of NBFRs in polar benthic marine sediment and food webs collected from areas around the Chinese Arctic Yellow River Station (n = 57) and Antarctic Great Wall Station (n = 94). ∑₇NBFR concentrations were in the range of 1.27-7.47 ng/g lipid weight (lw) and 0.09-1.56 ng/g lw in the Arctic and Antarctic marine biota, respectively, among which decabromodiphenyl ethane (DBDPE) was the predominant compound in all sample types. The biota-sediment bioaccumulation factors (g total organic carbon/g lipid) of NBFRs in the Arctic (0.85-3.40) were 4-fold higher than those in the Antarctica (0.13-0.61). Trophic magnification factors (TMFs) and their 95% confidence interval (95% CI) of individual NBFRs ranged from 0.43 (95% CI: 0.32, 0.60) to 1.32 (0.92, 1.89) and from 0.34 (0.24, 0.49) to 0.92 (0.56, 1.51) in the Arctic and Antarctic marine food webs, respectively. The TMFs of most congeners were significantly lower than 1, indicating a trophic dilution potential. This is one of the very few investigations on the trophic transfer of NBFRs in remote Arctic and Antarctic marine ecosystems, which provides a basis for exploring the ecological risks of NBFRs in polar regions.

Information about the occurrence and trophic transfer of polychlorinated naphthalenes (PCNs) in polar ecosystems is vital but scarce. In this study, PCNs were analyzed in benthic marine sediment and several biological species, collected around the Chinese polar scientific research stations in Svalbard in the Arctic and South Shetland Island in Antarctica. Total PCNs in biota ranged from 28 to 249 pg/g of lipid weight (lw) and from 11 to 284 pg/g lw in the Arctic and Antarctic regions, respectively. The concentrations and toxic equivalent (TEQ) of PCNs in polar marine matrices remained relatively low, and the compositions were dominated by lower chlorinated homologues (mono- to trichlorinated naphthalenes). Trophic magnification factors (TMFs) were calculated for congeners, homologues, and total PCNs in the polar benthic marine food webs. Opposite PCN transfer patterns were observed in the Arctic and Antarctic regions, i.e., trophic dilution and trophic magnification, respectively. This is the first comprehensive study of PCN trophic transfer behaviors in remote Arctic and Antarctic marine regions, providing support for further investigations of the biological trophodynamics and ecological risks of PCNs.