Residual levels, phase distributions, and human health risks of OCPs in the middle reach of the Huai River, China.

Are the residues of organochlorine pesticides (OCPs) in freshwater in China still of concern after prohibition and restriction for decades? The scarcity of monitoring data on OCPs in freshwater in China over the past few years has hampered understanding of this issue. In this study, water and suspended particulate matter (SPM) samples were collected from the middle reach of the Huai River for OCP analyses. Residues of ∑OCPs in water and SPM ranged from ND to 8.6 ng L-1 and 0.50 to 179 ng L-1, with mean concentrations of 1.7 ± 1.3 ng L-1 and 6.1 ± 31 ng L-1, respectively. ∑HCHs (α-, ß-, γ-, and δ-HCH) and ∑HEPTs (heptachlor and heptachlor epoxide) were the most predominant pesticides in the dissolved phase and SPM, respectively, accounting for 43 ± 35% and 27 ± 29% of ∑OCPs. HCHs and heptachlor epoxide mainly existed in the dissolved phase, while heptachlor mainly existed in SPM. The isomeric composition pattern of HCHs in water differed from that in SPM. Briefly, ß-HCH dominated in water, while δ-HCH dominated in SPM. However, the composition pattern of DDT and its metabolites in water was similar to that in SPM. o,p'-DDD and p,p'-DDE dominated in both water and SPM. The ratios of α-/γ-HCH and (DDD + DDE)/DDTs indicated that HCHs and DDTs were mainly derived from historical residues. Risk assessments indicated that OCPs may not pose carcinogenic and non-carcinogenic risks to residents.

Antagonistic Effects, Sources, and Distribution of Selenium and Toxic Metals in Fish from Selenium-Rich and High Cadmium Areas, Dashan Region, China.

The Gongxin River is one of the main rivers in the Dashan Region of Anhui Province in China, which is a Se-rich and high-Cd area, but no research has focused on the concentration, source, antagonism, and health risks of Se and TMs in fish. In this study, 120 fish samples (14 species), 24 sediment samples, and 24 water samples were collected to investigate the antagonistic effects, sources, and health risks of TMs and Se in fish from a typical selenium-rich and high cadmium region. Zn and Se in fish from the Gongxin River were higher than in the background, which might be attributed to the different feeding habits of different fish species. The apparent antagonism between Se and Cu, Pb, and Cd was explored, and the results showed that 30%, 75%, and 100% of the Se/Cu, Se/Pb, and Se/Cd ratios were greater than one, indicating that Cu, Pb, and Cd in fish might be combined with or detoxicated by Se. The source analysis of the elements showed that the geological background was the source of TMs and Se in fish samples. The amounts of Se and TMs were all within China's acceptable level guidelines, signifying no harm to citizens from eating fish.

Application of the multimedia fugacity model in predicting the environmental behaviors of PCBs: Based on field measurements and level III fugacity model simulation.

The comprehensive understanding of PCBs' fate has been impeded by the lack of simultaneous monitoring of PCBs in multiple environmental media in the background areas, which were considered long-term sinks for highly chlorinated PCBs. To address this gap, this study analyzed soils, willow tree barks, water, suspended particulate matter (SPM), and sediment samples collected from the middle reach of the Huaihe River in China for 27 PCBs. The results showed that the levels of ∑27PCBs in the soils were comparable to or lower than the background values worldwide. There were no significant correlations between organic matter and ∑27PCB concentrations in the soils and sediments. Additionally, the contamination of dioxin-like PCBs in the aquatic environment of the study area deserves more attention than in the soils. Applying the level III fugacity model to PCB 52, 77, 101, and 114 revealed that the soil was the primary reservoir, and air-soil exchange was the dominant intermedia transfer process, followed by air-water exchange. Furthermore, simulated results of air-soil and air-water diffusion were compared with those calculated from the field concentrations to predict the potential environmental behaviors of PCBs. Results indicated that the studied river would be a "secondary source" for PCB 52, 77, and 101. However, PCB 52, 77, 101, and 114 would continue to transfer from the air to the soil. This study combines multimedia field measurements and the fugacity model, providing a novel approach to predicting the potential environmental behaviors of PCBs.

Prioritization, sources, and ecological risk of typical antibiotics in the Huai River, a Chinese major river: a warning about aquaculture.

This is the first comprehensive report on antibiotics in the Huai River, a major Chinese river. To illuminate the concentrations, prioritization, spatial distributions, sources, and ecological risks of antibiotics, surface water samples were collected and three types of most widely used antibiotics (16 sulfonamides, 8 tetracyclines, and 14 quinolones) were analyzed. The results indicated that concentrations of ∑quinolones (86 ± 31 ng/L) > ∑tetracyclines (20 ± 13 ng/L) > ∑sulfonamides (11 ± 3.7 ng/L). Oxolinic acid (OXA), cinoxacin(CINX), norfloxacin (NFX), and methacycline (MTC) were the priority antibiotics with mean concentrations > or close to 10 ng/L, however, they were rarely included as target compounds in most previous Chinese investigations. Different spatial distributions of antibiotics were discovered across three reaches separated by two sluices, demonstrating that the sluices may impact antibiotic dissemination. According to the results of the source analysis, the aquaculture industry was the major source of observed antibiotics (49%), followed by livestock & poultry farming (26%) and mixed sources (25%). Because commercial fishing in the Huai River has been prohibited, the aquaculture industry will expand in the next years, and antibiotic contamination caused by the aquaculture industry deserves more attention. The risk quotients were calculated by comparing observed antibiotics to predicted no-effect concentrations, and the results showed that observed antibiotics posed negligible or low integrated risks for Green algae, and medium or low integrated risks for Daphnia magna.

Polycyclic aromatic compounds (PACs) in tree barks and tree cores of a national large-scale coal-fired power base of China: Sources, atmospheric toxicities, and pollution histories.

Polycyclic aromatic compounds (PACs) are important hazardous air pollutants in China due to the country's coal-dominant energy structure. In order to reveal the pollution characteristics, sources, toxicity, and pollution historical trends of PACs in the atmosphere of the middle reach of the Huaihe River (MRHR), a large-scale coal-fired power base of China, tree barks and tree cores were collected and employed as passive air samplers and historical trend recorders, and 76 PACs were identified for the first time. ΣPACs in tree barks ranged from 170 to 3800 ng g-1 (mean = 700 ± 720 ng g-1), with the high concentrations observed mainly in the coal-mining and coal-bearing area. 16 priority PAHs (PriPAHs) were the predominant substances and accounted for 59 ± 8.3 % of ΣPACs. The combustion of coal and fuel oil was the most significant source of PACs, accounting for 43 % of ΣPACs, followed by the combustion of biomass (30 %) and non-combustion sources (27 %). Based on a bark-air partitioning model, volumetric air concentrations for ΣPACs were calculated to be 450-11,000 ng m-3 (mean = 1600 ± 2000 ng m-3). The BaP-toxic equivalent concentrations (TEQBaP) of ΣPACs (mean = 9.7 ± 15 ng m-3) were significantly higher than the Chinese guideline (1 ng m-3) and were mostly caused by coal & fuel oil combustion (55 ± 13 %). High molecular weight PACs were detected in lower percentages in tree cores than in tree barks, indicating that PACs in the particle phase were difficult to enter the tree core. Major PACs decreased in tree core samples between 2000 and 2020 as pollution control efforts improved, however, some PACs showed different trends when influenced by point sources.

Selenium and toxic metals in human hair of the Dashan Region, China: Concentrations, sources, and antagonism effect.

The Dashan Region was a Se-rich region of China. In this study, 131 residents' human hair samples were collected. The concentrations of Se and toxic metals were analyzed, and the health risk was estimated using the concentration data. Cd and As concentrations were significantly higher than in East China. Se and most toxic metal concentrations increased with age (except for the aged people). Furthermore, gender and smoking habits might have a significant impact on toxic metals and Se levels. Multivariable statistics analysis revealed that Se and toxic metals primarily originate in the environment and are then transferred to the human body via the food chain. Dietary habits had an effect on the Se and As concentrations in hair, according to the results of stable isotope analysis. To assess detoxification ability, the Se/ toxic metal molar ratio was used as an indicator. The results demonstrated that the antagonistic effect of Se and Cd, As, Cr, and Hg (molar ratio > 1) could effectively protect residents in the study area from Cd and As pollution in daily life.

Organochlorine pesticides in riparian soils and sediments of the middle reach of the Huaihe River: A traditional agricultural area in China.

Distributions, souces, ecological risks as well as environmental behaviors of 20 organochlorine pesticides (OCPs) in riparian soils and sediments of the middle reach of the Huaihe River, a traditional agricultural area of China, were investigated. ∑OCPs in riparian soils and sediments were 1.8-63 ng g-1 (mean = 19 ± 12 ng g-1) and 1.2-9.9 ng g-1 (mean = 3.0 ± 1.8 ng g-1), respectively. HCHs were the dominant OCPs in both soils and sediments, while high concentrations of ∑HEPTs and ∑DDTs were also detected in some soils and sediments. No correlations were found between concentrations of OCPs and organic matter contents in both soils and sediments. Based on the source analysis, most OCPs in the riparian soils were mainly from historical residues, such as historical usage of technical HCH, DDT, chlordane and endosulfan. OCPs in sediments were influenced not only by surface runoff by also by other factors, e.g. in-situ contamination (DDT-containing antifouling paints in ships) and/or hydraulic transport from some tributaries. Some never-used OCPs, such as heptachlor and aldrin, were widely detected in soils and sediments. This might be attributed to some unknown usages or long-range atmospheric transport of them from other source regions. Ecological risk analysis suggested that DDTs and HCHs in soils would not lead to an adverse effect on soil ecological environment as well as agricultural production, and OCP residues in sediments also would not pose a threat to the sediment-dwelling organisms.

Polycyclic aromatic hydrocarbons (PAHs) in urban stream sediments of Suzhou Industrial Park, an emerging eco-industrial park in China: Occurrence, sources and potential risk.

In this study, urban stream sediment samples were collected in the Suzhou Industrial Park (SIP), one of the earliest national demonstration eco-industrial parks of China. PAHs were analyzed in these sediments, and concentrations of total PAHs were 180-81,000 ng g-1 (5700 ± 14,000 ng g-1). Medium molecular weight (4- ring) PAHs were predominant (42 ± 12%), followed by high molecular weight (5- and 6- ring) PAHs (31 ± 10%). No correlation was found between concentrations of PAHs and land uses of SIP in this study. Diagnostic ratios and a positive matrix factorization (PMF) model indicated that coal/biomass combustion might be the primary PAH source (61%), followed by non-combustion sources (21%) and vehicular emission (18%). According to the spatial analysis, PAHs in the sediments of SIP might be mainly associated with the coal/biomass combustion in the northeast industrial zone. Residential & commercial activities seem not to be the major causes of PAH contamination. Total PAH toxic equivalent concentrations, effect range low/effect range median values, and mean effects range-median quotient all showed that PAHs were present at a low toxicity risk level in most regions of the SIP. However, vigilance is required at some sampling sites with extremely high PAH concentrations or high mean effects range-median quotient.

Volatilization of polycyclic aromatic hydrocarbons (PAHs) over the North Pacific and adjacent Arctic Ocean: The impact of offshore oil drilling.

Air and seawater samples were collected in 2016 over the North Pacific Ocean (NPO) and adjacent Arctic Ocean (AO), and Polycyclic Aromatic Hydrocarbons (PAHs) were quantified in them. Atmospheric concentrations of ∑15 PAHs (gas + particle phase) were 0.44-7.0 ng m-3 (mean = 2.3 ng m-3), and concentrations of aqueous ∑15 PAHs (dissolved phase) were 0.82-3.7 ng L-1 (mean = 1.9 ng L-1). Decreasing latitudinal trends were observed for atmospheric and aqueous PAHs. Results of diagnostic ratios suggested that gaseous and aqueous PAHs were most likely to be related to the pyrogenic and petrogenic sources, respectively. Three sources, volatilization, coal and fuel oil combustion, and biomass burning, were determined by the PMF model for gaseous PAHs, with percent contributions of 10%, 44%, and 46%, respectively. The 4- ring PAHs underwent net deposition during the cruise, while some 3- ring PAHs were strongly dominated by net volatilization, even in the high latitude Arctic region. Offshore oil/gas production activities might result in the sustained input of low molecular weight 3- ring PAHs to the survey region, and further lead to the volatilization of them. Compared to the gaseous exchange fluxes, fluxes of atmospheric dry deposition and gaseous degradation were negligible. According to the extrapolated results, the gaseous exchange of semivolatile aromatic-like compounds (SALCs) may have a significant influence on the carbon cycling in the low latitude oceans, but not for the high latitude oceans.

Atmospheric organochlorine pesticides (OCPs) and polychlorinated biphenyls (PCBs) in the Antarctic marginal seas: Distribution, sources and transportation.

From November 2013 to March 2014, air samples were collected in the Antarctic marginal seas during the 30th Chinese Antarctic research expedition. Organochlorine pesticides (OCPs) and polychlorinated biphenyls (PCBs) were analyzed in these samples. The mean concentrations were observed for hexachlorobenzene (HCB) >ΣPCBs >Σhexachlorocyclohexanes(HCHs) >Σdichlorodiphenyltrichloroethane(DDTs)>Σchlordanes. High levels of HCB were found near east Antarctica and in the Ross Sea, reflecting the re-emission of HCB from environmental reservoirs of these regions. Parent DDTs (p,p'- and o,p'-DDT) were rarely detected, suggesting that atmospheric DDT was predominantly influencedby weathered DDT from some secondarysources. However, fresh inputs of DDTs could not be excluded because there were still some samples with high proportions of parent DDTs. HCHs only were detected in the South Indian Ocean (near Australia), andthis result might be related to the intense emissions of HCHs from southern Australia. Ratios of trans-chlordane/cis-chlordanein most samples were lower than that in technical chlordane, reflecting the main influence of weathered chlordane. High levels of ΣPCBs were found in the Ross Sea, suggesting an intense re-emission of PCBs. Furthermore, atmospheric PCBs near the Antarctic Peninsula were also relatively high, this finding might be attributed to the emissions of PCBs from nearby Antarctic research stations. Comparing with the Arctic, transport of OCPs and PCBs towards Antarctica is more difficult. The Antarctic marginal seas would act as both barriers and "buffer zones"during the transportation processes.

Sources, Fraction Distribution and Health Risk Assessment of Selenium (Se) in Dashan Village, a Se-Rich Area in Anhui Province, China.

Soil, rock, potable water, animal food and human hair samples were collected from the Dashan village, a typical selenium (Se)-rich area of China. Se content and fraction distribution were determined to trace the source of soil Se and evaluate the potential health risk to humans. Total Se contents in soils ranged from 0.60 to 10.46 mg kg- 1. The fractions of soil Se followed the order: residual Se (R-Se) > organic-bound Se (O-Se) > acid soluble Se (A-Se) > exchangeable Se (E-Se) > water soluble Se (W-Se). Total Se contents in rocks ranged from 0.07 to 24.8 mg kg- 1. The dietary Se intake of local residents was estimated to be 261.2 µg day- 1 and hair Se content varied from 0.34 to 1.35 mg kg- 1, suggesting that the potential health risk should be concerned. Weathering of carbonaceous rock was speculated to be the primary source of soil Se according to the contents of Se in rocks, the distribution of Se in soil profiles and the relationships between Se and other elements in soils and parent rocks.

CVD graphene as an electrochemical sensing platform for simultaneous detection of biomolecules.

The development of electrochemical biosensors for the simultaneous detection of ascorbic acid (AA), dopamine (DA), uric acid (UA), tryptophan (Trp), and nitrite ([Formula: see text]) in human serum is reported in this work. Free-standing graphene nanosheets were fabricated on Ta wire using the chemical vapor deposition (CVD) method. CVD graphene, which here served as a sensing platform, provided a highly sensitive and selective option, with detection limits of AA, DA, UA, Trp, and [Formula: see text] of 1.58, 0.06, 0.09, 0.10, and 6.45 µM (S/N = 3), respectively. The high selectivity of the electrode is here explained by a relationship between the bandgap energy of analyte and the Fermi level of graphene. The high sensitivity in the oxidation current was determined by analyzing the influence of the high surface area and chemical structure of free-standing graphene nanosheets on analyte adsorption capacity. This finding strongly indicates that the CVD graphene electrode can be used as a biosensor to detect five analytes in human serum.

Electrochemical Imprinted Polycrystalline Nickel-Nickel Oxide Half-Nanotube-Modified Boron-Doped Diamond Electrode for the Detection of L-Serine.

This paper presents a novel and versatile method for the fabrication of half nanotubes (HNTs) using a flexible template-based nanofabrication method denoted as electrochemical imprinting. With use of this method, polycrystalline nickel and nickel(II) oxide (Ni-NiO) HNTs were synthesized using pulsed electrodeposition to transfer Ni, deposited by radio frequency magnetron sputtering on a porous polytetrafluoroethylene template, onto a boron-doped diamond (BDD) film. The Ni-NiO HNTs exhibited semicircular profiles along their entire lengths, with outer diameters of 50-120 nm and inner diameters of 20-50 nm. The HNT walls were formed of Ni and NiO nanoparticles. A biosensor for the detection of L-serine was fabricated using a BDD electrode modified with Ni-NiO HNTs, and the device demonstrated satisfactory analytical performance with high sensitivity (0.33 µA µM(-1)) and a low limit of detection (0.1 µM). The biosensor also exhibited very good reproducibility and stability, as well as a high anti-interference ability against amino acids such as L-leucine, L-tryptophan, L-cysteine, L-phenylalanine, L-arginine, and L-lysine.

Methylmercury and trace elements in the marine fish from coasts of East China.

Fish consumption is an important source of human exposure to heavy metals. To determine the health risks for metals by consumption of marine fish in China, three species of fish, namely large yellow croaker (Pseudosciaena crocea), small yellow croaker (Pseudosciaena polyactis) and silver pomfret (Pampus argenteus) were collected and analyzed for methylmercury (MeHg), total mercury (T-Hg), selenium, cadmium, cobalt, chromium, copper, iron, manganese, nickel, lead, strontium and zinc. The large yellow croakers had the highest concentrations of mercury, lead, nickel and zinc, and the levels of MeHg were positively correlated to T-Hg. The ratios of MeHg to T-Hg in yellow croakers were significantly higher than those in silver pomfret, indicating differences in accumulation and magnification of MeHg in these two types of fish. The concentration of T-Hg was found to decrease as the Se level in fish tissues increased. Cadmium levels in 16% of the samples were higher than the criterion recommended by the European Commission Regulation. The concentrations of other metals were well below international standards. A human health risk assessment showed that the estimated daily intake of these metals did not exceed the reference dose established by the US Environmental Protection Agency. The hazard quotients (HQs) were all less than 1, indicating a situation of no risk for consumption of these fish.

Antigenic and immunogenic properties of truncated VP28 protein of white spot syndrome virus in Procambarus clarkii.

Previous studies identify VP28 envelope protein of white spot syndrome virus (WSSV) as its main antigenic protein. Although implicated in viral infectivity, its functional role remains unclear. In the current study, we described the production of polyclonal antibodies to recombinant truncated VP28 proteins including deleted N-terminal (rVP28ΔN), C-terminal (rVP28ΔC) and middle (rVP28ΔM). In antigenicity assays, antibodies developed from VP28 truncations lacking the N-terminal or middle regions showed significantly lowered neutralization of WSSV in crayfish, Procambarus clarkii. Further immunogenicity analysis showed reduced relative percent survival (RPS) in crayfish vaccinating with these truncations before challenge with WSSV. These results indicated that N-terminal (residues 1-27) and middle region (residues 35-95) were essential to maintain the neutralizing linear epitopes of VP28 and responsible in eliciting immune response. Thus, it is most likely that these regions are exposed on VP28, and will be useful for rational design of effective vaccines targeting VP28 of WSSV.

Evidence for cell apoptosis suppressing white spot syndrome virus replication in Procambarus clarkii at high temperature.

In shrimp, higher water temperatures (~32°C) can suppress the ability of white spot syndrome virus (WSSV) to replicate and cause mortality, but the mechanisms remain unclear. To investigate whether cell apoptosis might be involved, a Tdt-mediated dUTP nick-end label (TUNEL) method was used to assess levels of chromosomal DNA fragmentation in hepatopancreas and gill cells of Procambarus clarkii crayfish infected with WSSV and maintained at either 32 ± 1°C or 24 ± 1°C. Based on relative cell numbers with yellow-green colored TUNEL-positive nuclei, the apoptotic index was elevated in WSSV-infected crayfish maintained at 32°C. In gill tissue sections examined by transmission electron microscope, cells with nuclei displaying apoptotic bodies or marginated, condensed and fragmented chromatin without concurrent cell cytoplasm damage were also more prevalent. Flow cytometry sorting of annexin-stained cells showed apoptosis to be most prevalent in granular haemocytes, and assays for caspase-3 activity showed it to be most elevated in hepatopancreas tissue. Despite these indicators of cell apoptosis but consistent with WSSV replication being restricted at elevated temperatures, no increases in transcription of the viral anti-apoptosis genes ORF390 and ORF222 were detected by RT-PCR in shrimp maintained at 32°C, possibly due to the elevated levels of cellular apoptosis.

Polychlorinated biphenyls (PCBs) in marine fishes from China: levels, distribution and risk assessment.

Muscle tissues of large yellow croakers (Pseudosciaena crocea) and sliver pomfret (Pampus argenteus) from nine coastal cities of East China including Dalian, Tianjin, Qingdao, Shanghai, Zhoushan, Wenzhou, Fuzhou, Quanzhou and Xiamen were analyzed for polychlorinated biphenyl (PCB) concentrations. Thirty-six PCB congeners were quantified in the fishes, of which 11 congeners were dioxin-like PCBs. The total PCB concentrations of the present study were at the low end of the global range, which may be related to the smaller usage and shorter consumption history of PCBs in China. PCBs 18, 29, 52, 66, 101, 104, 138, 153, 180 and 194 were the major constituents found in the fish samples. Regression analysis showed a strong positive correlation (R(2)=0.800; p<0.001) between total dioxin-like PCBs and total PCB concentrations, and that total PCB concentrations explain 80% of the variability in total dioxin-like PCB concentrations. Among the species investigated, significantly higher concentrations of total PCBs were found in croakers than in pomfrets, which may be attributed to their different feeding and living habits. No significant difference in total PCB concentrations among the cities was observed; principal component analysis (PCA) of PCB profiles indicated that PCB pollution came from similar sources in the sampling areas and that there may be other PCB sources in Dalian and Wenzhou. The calculated carcinogenic risks (CRs) from the two species based on a low consumption group and high consumption group were all greater than 10(-6), suggesting that daily exposure to dioxin-like PCBs via fish consumption results in a lifetime cancer risk of greater than one in one million. In contrast, the hazard quotients (HQs) of noncancer risks were all less than unity.

Hexabromocyclododecanes (HBCDs) in marine fishes along the Chinese coastline.

This study reports concentrations of hexabromocyclododecanes (HBCDs) in two species of marine fish, large yellow croaker (Pseudosciaenacrocea) and silver pomfret (Pampusargenteus) (n = 46), from nine Chinese coastal cities (Dalian, Tianjin, Qingdao, Shanghai, Zhoushan, Wenzhou, Fuzhou, Quanzhou and Xiamen). HBCDs were detectable in all samples analyzed, indicating ubiquitous contamination of these compounds in the Chinese coastal environment. The average total HBCD concentration was 3.7 ng g⁻¹ lipid weight (range: 0.57-10.1 ng g⁻¹ lipid weight), which is relatively lower than other regions of the world, especially Europe, where HBCDs are intensively used. Among the three individual HBCD isomers (α-, ß- and γ-HBCD) in all fish samples, the α-isomer showed a remarkable predominance (from 87.5% to 100% of total contribution), indicating its higher bioaccumulative potential. Geographically, the highest HBCD level present in fish was found in Dalian in northern China, and the lowest occurred in Wenzhou. Estimated daily intakes of HBCDs via fish consumption for the Chinese population were 0.004-1.00 ng kg body weight⁻¹ d⁻¹. These exposure levels were much lower than the effect levels.

Levels and distribution of polybrominated diphenyl ethers (PBDEs) in marine fishes from Chinese coastal waters.

Concentrations of polybrominated diphenyl ethers (PBDEs) in yellow croakers (Pseudosciaena crocea) and silver pomfrets (Pampus argenteus) collected from nine coastal cities along the eastern China coastline were investigated. PBDE congeners with mono- to hexa-brominated substitutions were detected in the samples, indicating their ubiquitous distribution in the marine environment of China. The total PBDE concentration averaged 3.04 ng g⁻¹ lipid wt, a level that was relatively lower than in other regions of the world, especially North America where Penta-BDE was extensively used. Geographically, the highest concentration of PBDEs was found in Xiamen, and the PBDE levels in yellow croakers were significantly higher than those in pomfrets in most of the selected cities, a pattern which may be related to the different feeding habits of the two species. The congener profiles of PBDEs were found to be different from the commonly detected pattern in fishes from other regions of the world (i.e., BDE47>BDE99, BDE100>BDE153, BDE154). BDE47 and BDE154 were the predominant congeners in both species, accounting for more than 60% of the total PBDE concentrations. The reasons for the relatively high proportion of BDE154 may be due to the debromination of higher brominated congeners such as BDE183 and BDE209 by these two species.

Atmospheric HCH concentrations over the Marine Boundary Layer from Shanghai, China to the Arctic Ocean: role of human activity and climate change.

From July to September 2008, air samples were collected aboard the research expedition icebreaker XueLong (Snow Dragon) as part of the 2008 Chinese Arctic Research Expedition Program. Hexachlorocyclohexane (HCH) concentrations were analyzed in all of the samples. The average concentrations (± standard deviation) over the entire period were 33 ± 16, 5.4 ± 3.0, and 13 ± 7.5 pg m⁻³ for α-, ß- and γ-HCH, respectively. Compared to previous studies in the same areas, total HCH (ΣHCH, the sum of α-, ß-, and γ-HCH) levels declined by more than 10 × compared to those observed in the 1990s, but were approximately 4 × higher than those measured by the 2003 China Arctic Research Expedition, suggesting the increase of atmospheric ΣHCH recently. Because of the continuing use of lindane, ratios of α/γ-HCH showed an obvious decrease in North Pacific and Arctic region compared with those for 2003 Chinese Arctic Research Expedition. In Arctic, the level of α-HCH was found to be linked to sea ice distribution. Geographically, the average concentration of α-HCH in air samples from the Chukchi and Beaufort Seas, neither of which contain sea ice, was 23 ± 4.4 pg m⁻³, while samples from the area covered by seasonal ice (∼75°N to ∼83°N), the so-called "floating sea ice region", contained the highest average levels of α-HCH at 48 ± 12 pg m⁻³, likely due to emission from sea ice and strong air-sea exchange. The lowest concentrations of α-HCH were observed in the pack ice region in the high Arctic covered by multiyear sea ice (∼83°N to ∼86°N). This phenomenon implies that the re-emission of HCH trapped in ice sheets and Arctic Ocean may accelerate during the summer as ice coverage in the Arctic Ocean decreases in response to global climate change.