Impacts of shipyard oil leakage on the PAHs and PCBs occurrence in Xiangshan Bay, China.

Here, we studied the shipyard impacts on the distribution of PAHs and PCBs in the semi-enclosed Xiangshan Bay, an important mariculture zone in China. The results showed that the shipyard caused a pollution plume for PAHs but not for PCBs. As characteristic pollutants of oil leakage, the PAHs had concentrations of up to 55.82 ng L-1 in the water, 2235.04 ng g-1 in suspended particulate matter (SPM), and 1489.60 ng g-1 in sediment. The PAHs in water and SPM were dominated by phenanthrene and pyrene that were mostly derived from lubricant and diesel, while those in sediments were dominated by the high-molecular-weight PAHs, such as indeno[1,2,3-c,d]pyrene. In contrast, the PCBs concentrations reached up to 10.17 ng L-1, 79.72 ng g-1, and 124.33 ng g-1 in the seawater, SPM, and sediment samples, respectively, and they did not show spatial patterns affected by the shipyard. Moreover, the health risk assessment indicated that the shipyard discharge caused a substantial PAHs ecological risk to the adjacent and downstream water environment. Therefore, point source discharge in semi-enclosed bays should be paid close attention to due to the strong pollutant transport effect.

Impacts of haze on the photobleaching of chromophoric dissolved organic matter in surface water.

Sunlight plays an important role in the photochemical processes of chromophoric dissolved organic matter (CDOM), which is closely related to water self-purification and primary productivity of healthy aquatic ecosystem health. The fine particles of haze, a widespread air pollutant, absorb natural ultraviolet (UV) irradiation and have an unknown degree of influence on the photochemical transformation of CDOM. Here, an in-situ experiment investigating how the amount and composition of CDOM changes under hazy conditions was conducted in Ningbo, southeastern China, a city that frequently suffers from seasonal haze pollution. The results indicated that haze attenuated UV light under different weather conditions. The UV intensities were reduced from 1124.90 ± 91.58 to 510.26 ± 40.26 µW cm-2 and 748.54 ± 101.68 to 316.32 ± 40.48 µW cm-2 on sunny and cloudy days, respectively; these values approached those on rainy days (186.97 ± 28.58 µW cm-2). Consequently, the loss of dissolved organic carbon during the irradiation test was reduced on hazy days (e.g., from 5.63% to 2.59% on sunny/hazy days). The impact of haze on CDOM photobleaching was further assessed by an excitation-emission matrix (EEM) combined with parallel factor (PARAFAC) analysis. On hazy days, the EEM-PARAFAC components were saved from photobleaching to different degrees; and humic-like substances showed a stronger protective effect from haze than protein-like substances because of their higher photosensitivity. Consequently, haze could cause more terrestrial CDOM to remain in surface water. UV intensity played a critical role in the composition characteristics of CDOM. This study identifies the linkage between atmospheric pollution and water quality and demonstrates that long-term and large-scale haze may adversely influence aquatic ecology through pollutant/nutrient accumulation.