Hurricane resulted in releasing more nitrogenous than carbonaceous disinfection byproduct precursors in coastal watersheds.

The frequency of Atlantic hurricanes has been predicted to increase significantly by the end of this century. Watershed disturbance initiated by hurricanes can alter dissolved organic matter (DOM) quantity and quality in source water dramatically. DOM is an important disinfection by-product (DBP) precursor, and thus hurricanes can have a significant impact on water treatability and drinking water safety. The interactions between land use and land cover (LULC) of a watershed and DBP formation potential (FP) in source water under hurricane events have rarely been evaluated. Here, we quantified the FPs of two carbonaceous (trihalomethanes [THMs] and haloacetic acids [HAA]) and two nitrogenous (haloacetonitrile [HAN] and N-nitrosodimethylamine [NDMA]) DBPs at eighteen sub-watersheds with varying LULC along the Yadkin-Pee Dee River basin across North and South Carolina during and after the flooding condition caused by the 2016 Hurricane Matthew. Using chlorine as a disinfectant, THM FP was 238% (±117%) higher (p < .001) under the flooding condition than baseflow condition, while HAA FP did not change significantly as a result of the flooding. DOM composition under the flooding condition changed in favor of the formation of THMs rather than HAAs by a decrease of fulvic acid-like compounds and an increase in DOM aromaticity (SUVA). The FPs of studied DBPs under the flooding condition compared with the baseflow, followed the order of HAN (356.5%) > NDMA (246.4%) > THM (115.2%) using chloramine as a disinfectant. Higher HAN FP and NDMA FP compared to THM FP suggested that more nitrogenous than carbonaceous DBPs precursors were released during this hurricane event. LULC analysis revealed that forested wetlands were the major contributor of THM, HAA, and HAN precursors, whereas NDMA precursor was derived from developed areas. This unique study highlights the dynamic interplay between LULC and exports of carbonaceous and nitrogenous DBPs precursors during and after hurricanes.

Occurrence and distribution of microplastics at selected coastal sites along the southeastern United States.

To investigate the occurrence and distribution of microplastics in the southeastern coastal region of the United States, we quantified the amount of microplastics in sand samples from multiple coastal sites and developed a predictive model to understand the drift of plastics via ocean currents. Sand samples from eighteen National Park Service (NPS) beaches in the Southeastern Region were collected and microplastics were isolated from each sample. Microplastic counts were compared among sites and local geography was used to make inferences about sources and modes of distribution. Samples were analyzed to identify the composition of particles using Fourier transform infrared spectroscopy (FTIR). To predict the spatiotemporal distribution and movements of particles via coastal currents, a Regional Ocean Modeling System (ROMS) was applied. Microplastics were detected in each of the sampled sites although abundance among sites was highly variable. Approximately half of the samples were dominated by thread-like and fibrous materials as opposed to beads and particles. Results of FTIR suggested that 24% consisted of polyethylene terephthalate (PET), while about 68% of the fibers tested were composed of man-made cellulosic materials such as rayon. Based on published studies examining sources of microplastics, the shape of the particles found here (mostly fibers) and the presence of PET, we infer the source of microplastics in coastal areas is mainly from urban areas, such as wastewater discharge, rather than breakdown of larger marine debris drifting in the ocean. Local geographic features, e.g., the nearness of sites to large rivers and urbanized areas, explain variance in amount of microplastics among sites. Additionally, the distribution of simulated particles is explained by ocean current patterns; computer simulations were correlated with field observations, reinforcing the idea that ocean currents can be a good predictor of the fate and distribution of microplastics at the sites sampled here.

Occurrence of microplastics in the beach sand of the Chinese inner sea: the Bohai Sea.

The occurrence of microplastics in the beach sand of the Bohai Sea was investigated for the first time. The Bohai Sea is the largest Chinese inner sea and its coastal region is one of the most densely urbanized and industrialized zones of China. Samples from three costal sites (i.e., Bijianshan, Xingcheng and Dongdaihe) were collected, quantified and identified for microplastic analysis. Effects of sample depth and tourism activity were investigated. Surface samples (2 cm) contained higher microplastic concentrations than deep samples (20 cm). Samples from the bathing beach exhibited higher microplastic concentrations than the non-bathing beach, suggesting the direct contribution of microplastics from tourism activity. Of eight types of microplastics that were found, PEVA (polyethylene vinyl acetate), LDPE (light density polyethylene) and PS (polystyrene) were the largest in abundances. Moreover, the non-plastic items from samples were analyzed and results revealed that the majority abundance of the observed non-plastics were viscose cellulose fibers. Further studies are required to evaluate the environmental hazards of microplastics, especially as they may "act as a contaminant transporter" to the Bohai Sea ecosystem.