Ziwei Yao

Congener specific distributions of polybrominated diphenyl ethers (PBDEs) in sediment and mussel (Mytilus edulis) of the Bo Sea, China.

Congener specific distributions of polybrominated diphenyl ethers (PBDEs) were investigated in sediment and mussel (Mytilus edulis) collected from the coast of Bo Sea, China. The median values of BDE-209 and SigmaPBDEs (including BDE-17, -28, -47, -66, -71, -85, -99, -100, -138, -153, -154, -183 and -190) were 2.29 and 0.16 ng g(-1)dry weight in sediment, and 2.43 and 0.68 ng g(-1)dry weight in mussel, respectively. BDE-209 was the predominant congener (61-99% in mussel and 75-99% in sediment except for one sample with 17%). Different congener patterns (excluding BDE-209) were observed between sediment and mussel, which were attributed to individual congeners bioaccumulation potential and/or the ability to metabolize. The four most abundant congeners were BDE-47 (40.3%), -99 (22.5%), -71 (8.9%) and -28 (5.8%) in sediment, and -47 (36.4%), -28 (14.5%), -154 (8.6%) and -71 (8.6%) in mussel, respectively. The ratios of BDE-47/BDE-99 and BDE-100/BDE-99 in sediment were lower than those in mussel, indicating higher transformation and uptake rate of BDE-99 in mussel. The biota-sediment accumulation factor (BSAF) of individual PBDE congeners declined with the increase of their logarithm of octanol-water partition coefficients (log K(OW)) except for BDE-154, indicating congeners with higher logK(OW) were more likely to retain in sediment. These can be explained with a high affinity of these compounds for carbonaceous geosorbents, and molecular steric hindrance that limits large, very hydrophobic organic compounds from penetrating the cellular membranes.

Occurrence, distribution, and bioaccumulation of antibiotics in coastal environment of Dalian, China

Seawater, sediment, and aquatic organism samples were collected from 20 sampling sites in coastal environment of Dalian in August, 2011. The occurrence, distribution, and bioaccumulation of 20 antibiotics categorizing into three groups, including 14 sulfonamides (SAs), two chloramphenicols (CAPs) and four tetracyclines (TCs), were investigated. The results suggested that tetracyclines were the predominant antibiotics in the seawater (range: 2.11-9.23 ng L(-1)), while sulfonamides were the dominant antibiotics in both sediments (range: 1.42-71.32 μg kg(-1)) and aquatic organisms (range: 2.18-63.87 μg kg(-1)). The sorption coefficient Kd,s values revealed that sulfameter, sulfadiazine, sulfamethoxypyridazine, sulfamonomethoxine, chloramphenicol, and doxycycline presented higher sorption capacities than the other antibiotics. The average BAFs suggested that sulfamethazine, sulfamethiazole, sulfamonomethoxine, and doxycycline were potentially bioaccumulative, while sulfadiazine, sulfameter, sulfamethoxypyridazine, and chloramphenicol were bioaccumulative.

Bioaccumulation and Trophic Transfer of Short Chain Chlorinated Paraffins in a Marine Food Web from Liaodong Bay, North China

Short chain chlorinated paraffins (SCCPs) are under the evaluation for inclusion into the Stockholm Convention on persistent organic pollutants. However, information on their bioconcentration and biomagnification in marine ecosystems is unavailable, limiting the evaluation of their ecological risks. In this study, seawater, sediment, zooplankton, invertebrates, and fishes collected from Liaodong Bay, Bohai Sea, North China were analyzed to investigate the residual level, congener group profile, bioaccumulation, and trophic transfer of SCCPs in a marine food web. The total concentrations of SCCPs ranged from 4.1 to 13.1 ng L(-1) in seawater, 65 to 541 ng g(-1) (dw) in sediment, and 86 to 4400 ng g(-1) (ww) in organisms. Correspondence analysis indicated the relative enrichment of C10Cl5 and C11Cl5 formula groups in most aquatic organisms. Both the logarithm bioaccumulation factors (log BAFs: 4.1-6.7) and biota-sediment accumulation factors (BSAFs: 0.1-7.3) of individual congeners implied the bioaccumulation of SCCPs. The trophic magnification factor (TMF) of ∑SCCPs was determined to be 2.38 in the zooplankton-shrimp-fish food web, indicating biomagnification potential of SCCPs in the marine ecosystem. The TMF values of individual congener groups significantly correlated with their log KOW values.

Congener-specific distribution and bioaccumulation of short-chain chlorinated paraffins in sediments and bivalves of the Bohai Sea, China.

Short-chain chlorinated paraffins (SCCPs) are a new type of persistent organic pollutants that are of great environmental concern because of their wide distribution. In this study, surface sediments and bivalve samples were collected from the coastal area of the Bohai Sea in China. Total SCCP (ΣSCCP) concentrations in surface sediments and bivalves ranged from 97.4 ng g(-1) dry weight (dw) to 1756.7 ng g(-1) dw and 476.4-3269.5 ng g(-1) dw, respectively. C10-CPs and C11-CPs were the predominant homologue groups in all sediments and bivalves. Specific congener composition analysis and correspondence analysis indicated that the local SCCP source mainly came from CP-42 and CP-52 products, and riverine input had an important function. The biota-sediment accumulation factors of ΣSCCPs for bivalves ranged from 1.08 to 1.61, and a significant correlation indicated that the SCCP congener with higher chlorination degree was more likely to be accumulated in bivalves.

Correlations between physicochemical properties of PAHs and their distribution in soil, moss and reindeer dung at Ny-Ålesund of the Arctic

Concentrations of 16 polycyclic aromatic hydrocarbons (PAHs) in soil, moss and reindeer dung collected at Ny-Alesund of the Arctic were measured to investigate their accumulation trends and distribution in the three compartments. Compared with the other regions, the proportions of 2 + 3 ring PAHs to the total PAHs were higher, whereas the proportions of 5 + 6 ring PAHs were lower in the three compartments at Ny-Alesund. Significant log/log-linear relationship was observed between the sub-cooled liquid vapor pressure (p(L)( degrees )) and the soil/moss quotient (Q(SM)). The relation was similar to the relationship between the gas/particle partition coefficient (K(P)) and p(L)( degrees ) of PAHs, implying Q(SM) would be a mirror image of K(P). Excellent log/log-linear relationships were observed between Q(SM) and K(OA) as well as between the moss/dung quotient (Q(MD)) and K(OW). The results presented here indicate the physicochemical properties are suitable for characterizing the distribution of PAHs in soil, moss and reindeer dung.

Sulfonamide antibiotics in the Northern Yellow Sea are related to resistant bacteria: Implications for antibiotic resistance genes

Antibiotic resistance gene (ARG) residues and the mode of transmission in marine environments remain unclear. The sulfonamide (SAs) concentrations, different genes and total bacterial abundance in seawater and sediment of the Northern Yellow Sea were analyzed. Results showed the genes sul I and sul II were present at relatively high concentrations in all samples, whereas the gene sul III was detected fewer. The ARGs concentrations in the sediment were 10(3) times higher than those in water, which indicated sediment was essential ARG reservoir. Statistical analysis revealed the total antibiotic concentration was positively correlated with the relative abundance of the gene sul I and sul II. The relative abundances of the gene sul I and the gene sul II were also correlated positively with those of the gene int1. This correlation demonstrated that SAs exerted selective pressure on these ARGs, whereas the gene int1 could be implicated in the propagation of the genes sul I and sul II in marine environments.

Fate of sulfonamide resistance genes in estuary environment and effect of anthropogenic activities

With the exacerbating problem of antibiotic resistance, antibiotic resistance genes (ARGs) as emerging contaminants are found at elevated levels in inland aquatic environments, especially in regions of intensive agricultural and urban activity. However, little quantitative data exist on the migration and attenuation of ARGs in estuary ecosystem, which is central to predicting their fate after release into marine environment. Moreover, the relevance of multiple chemical contaminants and water quality constituents should be understood to amplify and attenuate antibiotic resistance levels. To determine the prevalence and examine the fate of sulfonamide ARGs (sul-ARGs) in two estuaries under different effects of anthropogenic activities, we analyzed the sul-ARGs (sul1, sul2, and sul3), class 1 integrons (int1), and bacterial biomass in surface water samples from Daliaohe and Liaohe river estuaries. We also evaluated five types of antibiotics, heavy metals, and various bulk water quality constituents. Results showed that sul-ARGs were widespread in Daliaohe and Liaohe river estuaries, but the distribution did not correlate with the concentration of sulfonamides. Significant reduction in the abundance of sul-ARGs was also observed with increased salinity. Nevertheless, the trend in the change of concentrations of sul-ARGs was different in the two estuaries. Statistical analysis of the results indicated that several metals were significantly and positively correlated with sul-ARGs. Pearsons correlation coefficients were higher than those determined between antibiotic residues and sul-ARGs. Furthermore, the relative abundance of sul-ARGs was significantly and positively correlated with the relative abundance of int1 which suggested that the propagation of sul-ARGs was facilitated by class 1 integrons in estuaries.

Distribution and characteristic of PAHs in snow of Fildes Peninsula.

Polycyclic aromatic hydrocarbons (PAHs) investigation in different matrices has been reported largely, whereas reports on snow samples were limited. Snow, as the main matrix in the polar region, has an important study meaning. PAHs in snow samples were analyzed to investigate the distribution and contamination status of them in the Antarctic, as well as to provide some references for global migration of PAHs. Snow samples collected in Fildes Peninsula were enriched and separated by solid-phase membrane disks and eluted by methylene dichloride, then quantified by gas chromatography/mass spectrometry. All types of PAHs were detected except for Benzo(a)pyrene. Principal component analysis method was applied to characterize them. Three factors (Naphthalene, Fluorene and Phenanthrene) accounted for 60.57%, 21.61% and 9.80%, respectively. The results showed that the major PAHs sources maybe the atmospheric transportation, and the combustion of fuel in Fildes Peninsula. The comparison of concentration and types of PAHs between accumulated snow and fresh snow showed that the main compound concentrations in accumulated snow samples were higher than those in fresh ones. The risk assessment indicated that the amount of PAHs in the snow samples would not lead to ecological risk.

Distribution characteristics and indicator significance of Dechloranes in multi-matrices at Ny-Ålesund in the Arctic

In recent years, Dechloranes have been widely detected in the environment around the world. However, understanding and knowledge of Dechloranes in remote regions, such as the Arctic, remain lacking. Therefore, the concentrations of 5 Dechloranes in surface seawater, sediment, soil, moss, and dung collected from Ny-Ålesund in the Arctic were measured with the concentrations 93 pg/L, 342, 325, 1.4, and 258 pg/g, respectively, which were much lower than those in Asian and European regions. The mean ratios of anti-Dechlorane Plus (DP) to total DP (ƒanti) in seawater, sediment, soil, moss, dung, and atmospheric samples were 0.36, 0.21, 0.18, 0.27, 0.66, and 0.43, respectively. Results suggested that the main source of DP in seawater, sediment, soil, and moss was long-range atmospheric transport. However, the ratio identified in dung was different, for which the migration behavior of the organism is probably the main source of DP.

Gas/particle partitioning of polycyclic aromatic hydrocarbons in coastal atmosphere of the north Yellow Sea, China

Samples of gas- and particle-phase polycyclic aromatic hydrocarbons (PAHs) were collected at three sampling stations (Xiaomai Island, Laohutan, and Zhangzi Island) in the north Yellow Sea, China during November 2008 and September 2009 to study their atmospheric transport potential and the gas/particle distributions. The composition of PAHs was dominated by gaseous compounds. The percentages of the particle-phase PAHs to the total concentrations were found to be higher during the heating period than the non-heating period. The ratios of naphthalene and acenaphthene to phenanthrene, chrysene and dibenzo(a,h)anthracene showed an increasing trend from Xiaomai Island to Zhangzi Island, which can be called as the local atmospheric distillation of PAHs. Gas/particle partitioning coefficients (Kp) and their relationship with the sub-cooled liquid vapor pressures (pºL) of PAHs were investigated. The regressions of logKp versus logpºL gave significant correlations for all samples of the three sites with r2 values in the range 0.56–0.66 (pu2009<u20090.01). Both Junge–Pankow adsorption model and octanol–air partition coefficient absorption model tended to underestimate the sorption for most PAHs, but the absorption model appeared to be more suitable for predicting the particle fraction of PAHs than the Junge–Pankow model.