Jianhui Tang

Occurrence and distribution of antibiotics in coastal water of the Bohai Bay, China: Impacts of river discharge and aquaculture activities

The presence of 21 antibiotics in six different groups was investigated in coastal water of the Bohai Bay. Meantime, to illuminate the potential effects caused by the river discharge and aquaculture activities, wastewater from three breeding plants and surface water from six rivers flowing into the Bohai Bay were also analyzed for the selected antibiotics. The result revealed that measured antibiotics in the North Bobai Bay were generally higher than those in the South, highlighting the remarkable effects of high density of human activities on the exposure of antibiotics in environment. The antibiotics found in the six rivers were generally higher than those in the Bohai Bay reflecting the important antibiotics source of river discharge. This study reveals that the high consumption of some antibiotics in aquaculture activities may pose high ecological risk to the bay.

Occurrence and risks of antibiotics in the Laizhou Bay, China: Impacts of river discharge

The presence of thirteen antibiotics categorized into four different groups (fluoroquinolones, macrolides, sulfonamides and trimethoprim) was investigated in the rivers discharging to the Laizhou Bay and the seawater of the bay, and the impacts of river discharge on the marine environment were assessed. The results revealed that the same antibiotics predominated in both the river water and the seawater. Additionally, the detected antibiotics in the river water were generally higher than those in the inner bay and in the open bay, reflecting the importance of the riverine inputs as a source of antibiotics. Risk assessment based on the calculated risk quotients (RQ) showed that enoxacin, ciprofloxacin, and sulfamethoxazole in the two aquatic environments both posed high ecological risks (RQ>1) to the most sensitive aquatic organisms Vibrio fischeri, Microcystis aeruginosa and Synechococcus leopoliensis, respectively.

Relationships of trace gases and aerosols and the emission characteristics at Lin'an, a rural site in eastern China, during spring 2001

A face milling tool comprises a holder and a bit of slice-like form of circular or lobed outline detachably secured on a seating by a screw or the like traversing a central aperture and presented so that the side wall is the rake face and the end face is the clearance face. The bit can be indexed on the securing means. A lobed bit has convex cutting edges of much larger radius than the average radius of the bit.

Occurrence and distribution of antibiotics in the Beibu Gulf, China: Impacts of river discharge and aquaculture activities

The occurrence and distribution of eleven selected antibiotics belonging to three groups were investigated in the Beibu Gulf. In addition, the potential effects of water discharged from four rivers and aquaculture activities were analyzed. Erythromycin-H₂O, sulfamethoxazole and trimethoprim were the most frequently detected compounds, with mean concentrations ranging from 0.51 to 6.30 ng L⁻¹. The concentrations of the rivers were generally higher than those of the gulf, implying that river discharge has an important effect on the Beibu Gulf. The concentrations of erythromycin-H₂O, sulfamethoxazole and sulfadimidine in the vicinity of aquaculture activities were higher, suggesting that a higher intensity of aquaculture activities could contribute to increasing levels of antibiotics in the environment. According to MEC (measured environmental concentration)/PNEC (predicted no-effect concentration), erythromycin, sulfamethoxazole and clarithromycin may present possible environmental risk to Pseudokirchneriella subcapitata, Synechococcus leopoliensis and P. subcapitata, respectively; therefore, attention should be given to the long-term ecological effects caused by the continuous discharge of antibiotics in the Beibu Gulf.

Preliminary measurements of aromatic VOCs in public transportation modes in Guangzhou, China

This study examined the exposure level of aromatic volatile organic compounds (VOCs) in public transportation modes in Guangzhou, China. A total of 40 VOC samples were conducted in four popular public commuting modes (subway, taxis, non-air-conditioned buses and air-conditioned buses) while traversing in urban areas of Guangzhou. Traffic-related VOCs (benzene, toluene, ethylbenzene, m/p-xylene and o-xylene) were collected on adsorbent tubes and analyzed by thermal desorption (TD) and gas chromatography/mass-selective detector (GC/MSD) technique. The results indicate that commuter exposure to VOCs is greatly influenced by the choice of public transport. For the benzene measured, the mean exposure level in taxis (33.6 microg/m(3)) was the highest and was followed by air-conditioned buses (13.5 microg/m(3)) and non-air-conditioned buses (11.3 microg/m(3)). The exposure level in the subway (7.6 microg/m(3)) is clearly lower than that in roadway transports. The inter-microenvironment variations of other target compounds were similar to that of benzene. The target VOCs were well correlated to each other in all the measured transports. The concentration profile of the measured transport was also investigated and was found to be similar to each other. Based on the experiment results, the average B/T/E/X found in this study was about (1.0/4.3/0.7/1.4). In this study, the VOC levels measured in evening peak hours were only slightly higher than those in afternoon non-peak hours. This is due to the insignificant change of traffic volume on the measured routes between these two set times. The out-dated vehicle emission controls and slow-moving traffic conditions may be the major reasons leading elevated in-vehicle exposure level in some public commuting journeys.

Occurrence and spatial distribution of organophosphate ester flame retardants and plasticizers in 40 rivers draining into the Bohai Sea, north China.

Organophosphate esters (OPEs) are alternatives to polybrominated diphenyl ethers, often used as flame-retardants and plasticizers. There are few reports of OPEs in river water. This study focused on the occurrence and spatial distribution of 11 OPE congeners and one synthetic intermediate triphenylphosphine oxide (TPPO) in 40 major rivers entering into the Bohai Sea. Total OPEs ranged from 9.6 to 1549 ng L(-1), with an average of 300 ng L(-1). Tris(1-chloro-2-propyl) phosphate (TCPP) (4.6-921 ng L(-1), mean: 186 ng L(-1)) and tris(2-choroethyl) phosphate (TCEP) (1.3-268 ng L(-1), mean: 80.2 ng L(-1)) were the most abundant OPEs and their distribution patterns are similar, indicating the same source (r = 0.61, P < 0.05) and the influence of large production and consumption of chlorinated OPEs in the region. Priority should be given to TCPP, PCEP and TPPO due to their high concentrations in the rivers and potential threat to aquatic organisms.

Occurrence and risks of antibiotics in the coastal aquatic environment of the Yellow Sea, North China

Eleven antibiotics in three different categories were investigated in two types of coastal bays (a semi-enclosed bay and an open bay) of the Yellow Sea and in fresh water (rivers and sewage treatment plants [STP] effluents) that discharged into the bays. The results revealed the presence of three predominant antibiotics: dehydration erythromycin, sulfamethoxazole and trimethoprim. These antibiotics were detected in the seawater and fresh water with concentrations of <0.23-50.4 ng L(-1) and <0.25-663.1 ng L(-1), respectively. In terms of the regional distribution of the compounds within the two types of bays, higher concentrations (<0.23-50.4 ng L(-1)) and higher spatial variations (coefficients of variation: 98%-124%) were found in the semi-enclosed Jiaozhou Bay due to the poor water-exchange ability and to fresh-water inputs through rivers and/or STP effluents. In contrast, lower concentrations (<0.23-3.0 ng L(-1)) and lower spatial variations (coefficients of variation: 36%-75%) were present in the open Yantai Bays due to the strong water-exchange with the open sea. The source apportionment suggested that 1) fresh-water inputs were the primary source of macrolides in the coastal water, and 2) mariculture affected the relative pollution levels of trimethoprim, sulfamethoxazole and sulfathiazole in the bays. In addition, a risk assessment based on the calculated risk quotient (RQ) showed that the dehydrated erythromycin, sulfamethoxazole and clarithromycin detected at most of the sampling sites in Jiaozhou Bay could pose high (RQ>1) risks to the most sensitive aquatic microorganisms, such as Synechococcus leopoliensis and Pseudokirchneriella subcapitata, whilst in the Yantai Bays, the compounds could pose medium risks (1≥RQ>0.1) to the same aquatic microorganisms.

Source of surface ozone and reactive nitrogen speciation at Mount Waliguan in western China : new insights from the 2006 summer study

measurement period of 2006 (55%) than that of 2003 (25%). The abnormally high values of NOy observed in 2003 were suspected to be due to the positive interference from ammonia (NH3) to the particular catalytic converter used in that study. Varied diurnal patterns were observed for the various NOy components. The ozone production efficiencies (DO3/DNOz), which were estimated from the slope of the O3‐NOz scatterplot, were 7.7–11.3 for the polluted plumes from central and eastern China. The speciation of reactive nitrogen was investigated for the first time in the remote free troposphere in western China. PAN and particulate NO3 − were the most abundant reactive nitrogen species at WLG, with average proportions of 32% and 31%, followed by NOx (24%) and HNO3 (20%). The relatively large contribution of particulate NO3 − to NOy was due to the presence of high concentrations of NH3 and crustal particles, which favor the formation of particulate nitrate. An analysis of backward trajectories for the recent 10 years revealed that air masses from central and eastern China dominated the airflow at WLG in summer, suggesting strong impact of anthropogenic forcing on the surface ozone and other trace constituents on the Plateau.

Distribution and air-sea exchange of current-use pesticides (CUPs) from East Asia to the high Arctic Ocean.

Surface seawater and marine boundary layer air samples were collected on the ice-breaker R/V Xuelong (Snow Dragon) from the East China Sea to the high Arctic (33.23-84.5° N) in July to September 2010 and have been analyzed for six current-use pesticides (CUPs): trifluralin, endosulfan, chlorothalonil, chlorpyrifos, dacthal, and dicofol. In all oceanic air samples, the six CUPs were detected, showing highest level (>100 pg/m(3)) in the Sea of Japan. Gaseous CUPs basically decreased from East Asia (between 36.6 and 45.1° N) toward Bering and Chukchi Seas. The dissolved CUPs in ocean water ranged widely from <MDL to 111 pg/L. Latitudinal trends of α-endosulfan, chlorpyrifos, and dicofol in seawater were roughly consistent with their latitudinal trends in air. Trifluralin in seawater was relatively high in the Sea of Japan (35.2° N) and evenly distributed between 36.9 and 72.5° N, but it remained below the detection limit at the highest northern latitudes in Chukchi Sea. In contrast with other CUPs, concentrations of chlorothalonil and dacthal were more abundant in Chukchi Sea and in East Asia. The air-sea gas exchange of CUPs was generally dominated by net deposition. Latitudinal trends of fugacity ratios of α-endosulfan, chlorothalonil, and dacthal showed stronger deposition of these compounds in East Asia than in Chukchi Sea, while trifluralin showed stronger deposition in Chukchi Sea (-455 ± 245 pg/m(2)/day) than in the North Pacific (-241 ± 158 pg/m(2)/day). Air-sea gas exchange of chlorpyrifos varied from net volatilizaiton in East Asia (<40° N) to equilibrium or net deposition in the North Pacific and the Arctic.

Distribution and long-range transport of polyfluoroalkyl substances in the Arctic, Atlantic Ocean and Antarctic coast.

The global distribution and long-range transport of polyfluoroalkyl substances (PFASs) were investigated using seawater samples collected from the Greenland Sea, East Atlantic Ocean and the Southern Ocean in 2009-2010. Elevated levels of ΣPFASs were detected in the North Atlantic Ocean with the concentrations ranging from 130 to 650 pg/L. In the Greenland Sea, the ΣPFASs concentrations ranged from 45 to 280 pg/L, and five most frequently detected compounds were perfluorooctanoic acid (PFOA), perfluorohexanesulfonate (PFHxS), perfluorohexanoic acid (PFHxA), perfluorooctane sulfonate (PFOS) and perfluorobutane sulfonate (PFBS). PFOA (15 pg/L) and PFOS (25-45 pg/L) were occasionally found in the Southern Ocean. In the Atlantic Ocean, the ΣPFASs concentration decreased from 2007 to 2010. The elevated PFOA level that resulted from melting snow and ice in Greenland Sea implies that the Arctic may have been driven by climate change and turned to be a source of PFASs for the marine ecosystem.