Behavioral and ecotoxicology of sulfonamide metabolites in the aquatic environment.

Sulfonamides (SAs) are the first broad-spectrum synthetic antimicrobial agents used in human health and veterinary medicine. The majority of SAs entering human body is discharged into aquatic environment in the form of parent material or metabolites. The residues of SAs and their metabolites in the aquatic environment and the development of drug resistance can be serious threats to ecosystems and human health. We summarized recent advances in the research of SAs. The main metabolite types of SAs and the distribution characteristics of metabolites in different aquatic environments were introduced. The ecotoxicology of SAs metabolites, especially the distribution and hazards of sulfonamide resistance genes (sul-ARGs), were discussed with emphasis. Finally, the future research works were proposed. This paper could provide basic information for further research on SAs.

Heavy metal mobility in contaminated sediments under seawater acidification.

The behavior of heavy metals in contaminated sediment is of ecological significance considering the change of pH caused by ocean acidification. This study investigated the mobility of Cd, Cu, Ni, Pb, Fe, and Mn under experimental conditions for seawater acidification via enrichment of CO2 gas at different reaction set-ups. The results indicated that the concerned metals behaved differently in the water compared to the sediment. The heavy metals were considerably transferred from sediment to seawater, and the resultant intensity was controlled by the degree of acidification and the chemical state of specific metals. Moreover, labile fractions of heavy metals in sediments were more susceptible to acidification than other fractions. These findings were observed and confirmed using real-time monitoring conducted via the diffusion gradient technique (DGT). Overall, the results of this study provided new insights into exploring the coupling risk of heavy metals with ocean acidification.

Historical evolutions of sediment quality in bays under serious anthropogenic influences in China, basing on fuzzy comprehensive assessment of heavy metals.

Fuzzy comprehensive assessment was applied, for the first time, to investigate the sediment environmental quality and compare the historical variations of heavy metal pollution in Daya Bay and Jiaozhou Bay, which are representative for sub-tropical and temperate zone of China, respectively. Results shown the Daya Bay had undergone three contrasting stages in the past 100 years. Before 1980s, the sediment was not contaminated by metals and its quality generally conformed to class I of China National Standard for marine sediment quality. During from 1980s to 2000s, however, Daya Bay's environment had experienced significant deterioration. The metal concentrations were significantly higher than the background values, suggesting that there was a sharp increase of metal input. The category of sediment quality fell to class II and class III. Copper was the dominant pollutant during that time. The good thing is sediment quality of Daya Bay has improved to class I since 2000s, and chromium turned to be the major pollutant. As for the Jiaozhou Bay, enrichment of heavy metal was generally not detected and the sediment quality strictly conformed to class I during the recent 90 years. Chromium and zinc were the major pollutants in this bay.

Intensive anthropogenic activities had affected Daya Bay in South China Sea since the 1980s: Evidence from heavy metal contaminations.

Sediment geochemical characteristics were analyzed to assess how anthropogenic activities affected the Daya Bay, a subtropics bay adjacent to the most economically developed region of China. Vertical profiles of heavy metal contents and their enrichment factors indicated the development of Daya Bay environment in the past 100 years basically experienced three stages, which were closely consistent with the economic development. Before 1980s, the concentration of heavy metals was basically at the background level. Contamination of metals, particularly for Cr, Ni, Cu, Zn, Cd, and Pb, generally began in mid-1980s and became serious in 2000s. However, after late-2000s, the sediment quality had been radically improved. Heavy metals in nearshore sediment of Daya Bay were all closely related with import of anthropogenic and/or terrestrial material, whereas those in offshore were likely to be related with joint influence from the anthropogenic activities and the natural processes.

Source identification and risk assessment based on fractionation of heavy metals in surface sediments of Jiaozhou Bay, China.

To identify sources and evaluate ecological risks of heavy metals in sediments of Jiaozhou Bay, contents and chemical fractions of Cd, Cr, Cu, Pb, Zn, Ni, Sb and Sn were studied. Results suggested that higher metal contents appeared at inner bay and near marine dumping area. Labile fractions of heavy metals accounted for 0.5-77% (~36%) of total contents indicating their significant anthropogenic sources. The enrichment levels of Cd and Sb were relatively higher. Cu, Ni, Cd and Zn were at low to medium risks. Cr, Pb, Sn and Sb were at no or low risks. Total contents of heavy metals were mainly controlled by natural sources, while anthropogenic inputs were important sources of labile fractions of heavy metals in sediments of Jiaozhou Bay with industrial and domestic activities as main contributors for Cu, Pb, Zn, Cr, Ni and Sn, and agricultural activities for Cd and regional coal combustion for Sb.

Metals in size-fractionated core sediments of Jiaozhou Bay, China: Records of recent anthropogenic activities and risk assessments.

Total contents and chemical speciation of Co, Ni, Cu, Ga, Mo, Cd, In, Sn, Sb, V, W, Tl, Bi and U in size-fractionated (<32, 32-63 and >63µm) core sediments from Jiaozhou Bay were investigated to reveal their responses to anthropogenic activities. Metal contents showed a decreasing trend with increasing grain sizes. However, the loadings of metal fraction on <32, 32-63 and >63µm grain sizes were 16%, 47% and 37%, respectively. Anthropogenic fluxes and enrichment factors of metals in >63µm fraction were closely linked to anthropogenic activities, with an obvious increase in upper 27cm (1998-2015) and a slight decrease in 2009year. Metals (especially for Cd, Co, Cu and Ni) in >63µm fraction were more easily released, with the highest percentage of acid soluble form and lowest residual form. Thus, the size fraction of >63µm cannot be ignored.

Speciation of heavy metals in different grain sizes of Jiaozhou Bay sediments: Bioavailability, ecological risk assessment and source analysis on a centennial timescale.

Heavy metal contamination is an essential indicator of environmental health. In this work, one sediment core was used for the analysis of the speciation of heavy metals (Cr, Mn, Ni, Cu, Zn, As, Cd, and Pb) in Jiaozhou Bay sediments with different grain sizes. The bioavailability, sources and ecological risk of heavy metals were also assessed on a centennial timescale. Heavy metals were enriched in grain sizes of < 63µm and were predominantly present in residual phases. Moreover, the mobility sequence based on the sum of the first three phases (for grain sizes of < 63µm) was Mn > Pb > Cd > Zn > Cu >Ni > Cr > As. Enrichment factors (EF) indicated that heavy metals in Jiaozhou Bay presented from no enrichment to minor enrichment. The potential ecological risk index (RI) indicated that Jiaozhou Bay had been suffering from a low ecological risk and presented an increasing trend since 1940s owing to the increase of anthropogenic activities. The source analysis indicated that natural sources were primary sources of heavy metals in Jiaozhou Bay and anthropogenic sources of heavy metals presented an increasing trend since 1940s. The principal component analysis (PCA) indicated that Cr, Mn, Ni, Cu and Pb were primarily derived from natural sources and that Zn and Cd were influenced by shipbuilding industry. Mn, Cu, Zn and Pb may originate from both natural and anthropogenic sources. As may be influenced by agricultural activities. Moreover, heavy metals in sediments of Jiaozhou Bay were clearly influenced by atmospheric deposition and river input.

Atmospheric wet deposition of dissolved trace elements to Jiaozhou Bay, North China: Fluxes, sources and potential effects on aquatic environments.

To analyze the fluxes, seasonal variations, sources and potential ecological effects of dissolved trace elements (TEs) in atmospheric wet deposition (AWD), one-year wet precipitation samples were collected and determined for nine TEs in Jiaozhou Bay (JZB) between June 2015 and May 2016. Both the volume-weighted mean (VWM) concentration and flux sequence for the measured TEs was Al > Mn > Zn > Fe > Pb > Se > Cr > Cd > Co. Al was the most abundant TE with a VWM concentration and wet flux of 33.8 µg L-1 and 29.2 mg m-2 yr-1, which were 2 and 3 orders of magnitude higher than those of Co, respectively. The emission intensities of pollutants, rainfall amount and wind speed were the dominating factors influencing seasonal variations of TEs in AWD. Based on enrichment factors, correlation analysis and principal component analysis, most of the TEs in AWD were primarily originated from anthropogenic activities except for Al and Fe, which are typically derived from re-suspended soil dusts. Although the TE inputs by AWD were significantly lower than those by rivers, the TE inputs via short-term heavy rains would distinctly increase surface seawater TE concentrations and then pollute the marine environment of JZB. AWD would have both profound impacts on the biogeochemical cycles of TEs and dual ecological effects (nutrient and toxicity) on aquatic organisms.

[Distribution and Sources of n-alkanes in Surface Seawater of Jiaozhou Bay].

Hydrocarbons emitted by human activities probably constitute the largest class of contaminants that are present in coastal areas, because of widespread use of fossil fuels for power generation and logistics, and accidental spillages. The chemical composition of hydrocarbon mixtures found in the marine environment allowed the identification of relative contributions of different natural and anthropogenic sources. Identification of these hydrocarbons, especially n-alkanes, could act as tracers for the possible sources. To evaluate n-alkanes concentrations with emphasis on source analysis, surface water without visible oil was collected from the cruise in April 2016. Determination and quantification were performed by solvent extraction and gas chromatography-mass spectrometry. Various molecular diagnostic parameters were used to assess the contribution of different sources and origin of n-alkanes in surface seawater of Jiaozhou Bay. Concentrations of total dissolved n-alkanes(C11-C37) were between 1.756-39.09 µg·L-1 with a high carbon number predominance profile without odd-even carbon number preference. The n-alkane concentrations varied spatially depending on the distance away from main input sources and the ability of water exchange. It was at a higher concentration in the northeast and west coastal areas, as well as the mouth of Jiaozhou Bay. And concentrations were relatively lower in the inner area and outside of Jiaozhou Bay. In the sea area with strong water exchange, concentrations of total n-alkanes were around 2.196 µg·L-1, which could be considered as the environmental background level of n-alkanes in Jiaozhou Bay. Those n-alkanes were dominated with C24, with a slightly odd carbon number preference in low carbon n-alkanes and an even carbon number preference in high carbon n-alkanes. The values of CPI for the whole range of n-alkanes series, low carbon n-alkanes, and high carbon n-alkanes were 0.949, 1.026, and 0.980, respectively. Diagnostic indices and curves indicated that the dominant inputs of those n-alkanes were from marine biogenic input such as algae and marine bacteria. The concentration profiles of n-alkanes in other areas were characterized by no odd-even predominance in the range of C21-C33 with peaks center at C24 which were indicative of anthropic contributions as emission sources. N-alkanes dominating with anthropic sources comprised a high proportion(83.7%) of total n-alkanes. Activities of harbors and ships were the main contributors of Jiaozhou Bay n-alkanes. Physical processes, such as evaporation and dilution, were the principal weathering mechanisms. Because of its sufficient environmental capacity, Jiaozhou Bay was still moderately contaminated with petroleum.