Search Results (2)

Microplastics (MPs), defined as plastic particles of less than 5 mm, pose a significant global environmental threat, particularly in aquatic ecosystems, due to their persistence and potential harmful effects on wildlife and human health. They can absorb persistent organic pollutants (POPs), like polycyclic aromatic hydrocarbons (PAHs) and polychlorinated biphenyls (PCBs), raising concerns about their impact on biota. To elucidate this impact, the present study employed attenuated total reflectance Fourier transform infrared spectroscopy (ATR-FTIR) to analyse the characteristics of MPs sourced from commercial cosmetics. We investigated the toxicity of MPs on Caenorhabditis elegans and two entomopathogenic nematode species, Steinernema feltiae (the enviroCORE strain SB12(1)) and Steinernema carpocapsae (a commercial strain from e-NEMA) in laboratory bioassays. Nematodes were exposed to various concentrations of MPs and other pollutants, including atrazine, 1,3-dichloropropene, naphthalene, and fluorene, in controlled settings over 72 to 96 h. Additionally, high-throughput 18S rDNA sequencing was used to analyse nematode biodiversity in sediments from the River Barrow (RB) in SE Ireland. Our findings revealed that MPs increased nematode mortality and adversely affected community structure, as indicated by nematode maturity and sigma maturity indices, suggesting a potential disruption of the ecological balance in river sediments. This highlighted the ecological risks posed by MP pollution and emphasised the urgent need for further research into the health of benthic ecosystems in Ireland, particularly in relation to how MPs may influence nematode community dynamics and biodiversity. Full article

In September 2009, a series of sediment cores were collected across the Alaskan Beaufort Sea shelf-slope. Sediment and porewater organic carbon (OC) concentrations and stable carbon isotope ratios (δ¹³C) were measured to investigate spatial variations in sediment organic matter (OM) sources and distribution of these materials across the shelf. Cores were collected along three main nearshore (shelf) to offshore (slope) sampling lines (transects) from east-to-west along the North Slope of Alaska: Hammerhead (near Camden Bay), Thetis Island (near Prudhoe Bay), and Cape Halkett (towards Point Barrow). Measured sediment organic carbon (TOC) and porewater dissolved organic carbon (DOC) concentrations and their respective δ¹³C values were used to investigate the relative contribution of different OM sources to sediment OC pool cycled at each location. Sources of OM considered included: water column-sourced phytodetritus, deep sediment methane (CH₄), and terrestrial, tundra/river-sourced OM. Results of these measurements, when coupled with results from previous research and additional analyses of sediment and porewater composition, show a pattern of spatial variation in sediment OC concentrations, OM source contributions, and OM cycled along the Alaskan Beaufort Sea shelf. In general, measured sediment total organic carbon (TOC) concentrations, δ¹³C_TOC values, porewater DOC concentrations, and δ¹³C_DOC values are consistent with an east-to-west transport of modern Holocene sediments with higher OC concentrations primarily sourced from relatively labile terrestrial, tundra OM sources and phytodetritus along the Alaskan Beaufort shelf. Sediment transport along the shelf results in the medium-to-long term accumulation and burial of sediment OM focused to the west which in turn results in higher biogenic CH₄ production rates and higher upward CH₄ diffusion through the sediments resulting in CH₄⁻AMO-sourced contribution to sediment OC westward along the shelf. Understanding current OM sources and distributions along the Alaskan Beaufort shelf is important for enhancing models of carbon cycling in Arctic coastal shelf systems. This will help support the prediction of the climate response of the Arctic created in the face of future warming scenarios. Full article