北京城区屋面径流中PAHs的污染特征与来源解析

以北京典型城区屋面径流中的PAHs为研究对象,在2008年雨季采集了不同地点的屋面径流,分析了溶解相和颗粒相PAHs的质量浓度,对屋面径流中PAHs的质量浓度特征、时空变化规律及来源进行了讨论。结果表明,屋面径流具有较严重的PAHs污染,16种PAHs在溶解相中的总质量浓度为563.85~937.01 ng.L-1,来源主要是机动车排放（31.9%）、煤燃烧（39.6%）、天然气燃烧（15.3%）及石油类的挥发（14.2%）;在颗粒相中的总质量浓度为844.48~1372.62 ng.L-1,来源主要包括燃煤（51.8%）、汽油（38.1%）和柴油（10.1%）的燃烧等。BaP的EMC平均值（172 ng.L-1）远远超过我国污水排放标准（30 ng.L-1）,且以颗粒相为主。不同地点采集的屋面径流中的PAHs质量浓度大部分表现出较明显的初期效应和时间变化,而在不同采样点之间则没有明显的空间差异。     

扩散管差分法测定大气中氨和颗粒物铵盐

本文用扩散管差分法和多种叠层滤膜法大气中颗的铵盐和气态氨，扩散管关分法可以有铲分离测量颗粒物铵盐和气态氨，避免了采样时惰性上颗粒物硝酸铵分解的人为影响。     

北京东南郊大气中多环芳烃的相分配及其致癌毒性表征

采用索氏提取法提取2005年3月至2006年1月间北京市东南郊3个采样点大气总悬浮颗粒物(TSP)样品和气相样品中的多环芳烃(PAHs),利用GC/MS分析其质量浓度,对PAHs在颗粒相和气相间的分配行为进行研究。结果表明,2环组分在气相PAHs中占优势地位,全年平均在95%左右;4环组分在颗粒相PAHs中全年平均占56%左右;5~6环组分几乎全部分布在颗粒相中。引入苯并[a]芘等当量毒性因子(TEFs),探讨致癌毒性组分在2相间的分配行为,研究发现低毒高质量浓度的低环组分与高毒低质量浓度的高环组分对致癌性贡献相当;利用苯并[a]芘等效质量浓度与16种PAHs组分质量浓度进行多元线性回归,得到的回归方程用于粗略计算大气中PAHs致癌性组分的等效质量浓度;在分析PAHs分配行为的季节变化规律基础上,结合气象参数和空气污染指数分析PAHs在大气气相和颗粒相中分配系数的影响因素,并提出了分配系数与气象参数和API指数的回归方程,并利用回归方程来计算PAHs组分在大气中的分配系数。     

Distribution and vertical migration of polycyclic aromatic hydrocarbons in forest soil pits of southeastern Tibet

PAHs could be transported to Tibetan Plateau in accompany with atmospheric circulation. The forest regions were found be an important sink for PAHs, while their distributions and migrations in forest are still uncertain. In this study, soil profile samples were collected in southeastern Tibet and the concentrations, distributions, and migration of PAHs in forest region were investigated. The PAHs levels in the forest soils were at the low end of remote sites, ranged from 27.4 to 120.3 ng g^?1 on a dry weight based. Due to low ambient temperature and high organic carbon content, enrichment of PAHs was found in higher altitude on north side. According to the soil profiles, the vertical distributions of PAHs in organic layers were mainly influenced by pedogenesis, while the vertical distributions in mineral layers were dominated by downward leaching effect. Enrich factor (EF) of PAHs was estimated, and the values in organic layers were positively correlated with the octanol–air partition coefficients (K _OA), but EFs in mineral layers decreased with the K _OA values. PAHs in the surface soils on the north side of forest were relatively stable, while the migration of PAHs on the south sides and other clearing sites was more active. The leaching rates of PAHs in clearing site ranged between 1.42 and 29.3%. The results from this study are valuable on the characterization of PAHs in Tibetan Plateau.     

Pah characteristics in ambient air within a steel industrial complex

Ambient air samples at ten sites in an iron and steel industrial complex were collected from June to December for analyzing polycyclic aromatic hydrocarbons (PAHs). Sixteen species of PAH components in air samples were identified. The results indicate that both gaseous phase and particle‐bound PAHs at the top of the cokemaking plants are unusually high. The profiles of particle‐bound PAHs indicate that the predominant species at the top of, the coke oven batteries are those of high molecular weight components. The major components of particle‐bound PAHs at sampling sites near the fenceline, however, include the medium molecular weight components. The PAH profiles of air samples within the industrial complex show a strong similarity to those of cokemaking plant samples. The concentrations and the specific content of benzo(a)pyrene in the iron and steel industrial complex are higher than those values measured in urban area, petrochemical industry park, and open‐air burning area.     

Polycyclic aromatic hydrocarbons in red mullet (Mullus bavbatus) and sediments from the Eastern Aegean Sea

The distribution of polycyclic aromatic hydrocarbons (PAHs) was investigated in red mullet (Mullus barbatus) and sediment samples in the eastern Aegean Sea. The data were collected during cruises in July and November 1994, in the framework of National Marine Measurement and Monitoring Programme in the Aegean Sea. PAHs were detected in the tissue of Mullus barbatus of different sex and size from nine sampling sites throughout the study area ranging from 0.03 to 0.46 ug/g (fresh weight). The observations show the high levels of PAHs were found in tissues of females. The average concentration of PAHs in Aegean Sea sediments ranged from 0.20 to 1.8 ug/g (dry weight). No significant correlation was observed between PAH and sedimentary organic carbon.     

Occurrence and particle-size distributions of polycyclic aromatic hydrocarbons in the ambient air of coking plant

The purpose of this study was to characterize the occurrence and size distributions of ten species of polycyclic aromatic hydrocarbons (PAHs) in the ambient air of coking plants. Particulate-matter samples of four size fractions, including ≤2.1, 2.1–4.2, 4.2–10.2, and ≥10.2 μm, were collected using a Staplex234 cascade impactor during August 2009 at two coking plants in Shanxi, China. The PAHs were analyzed by a gas chromatograph equipped with a mass-selective detector. The concentrations of total particulate-matter PAHs were 1,412.7 and 2,241.1 ng/m³ for plants I and II, and the distributions showed a peak within the 0.1–2.1 μm size range for plant I and the 0.1–4.2 μm for plant II. The size distributions of individual PAHs (except fluoranthene) exhibited a considerable peak within the 0.1–2.1 μm size range in coking plant I, which can be explained by the gas–particle partition mechanism. The ambient air of the coking plant was heavily polluted by PAHs associated with fine particles (≤2.1 μm), and benzo[b]fluoranthene made the largest contribution to total PAHs. The exposure levels of coking-plant workers to PAHs associated with fine particles were higher than to PAHs associated with coarse particles. Benzo[b]fluoranthene, benzo[a]pyrene, and dibenzo[a,h]anthracene should be the primary pollutants monitored in the coking plant. This research constitutes a significant contribution to assessing the exposure risk of coking-plant workers and providing basic data for PAH standards for ambient air in coking plants.     

Particle-bound polycyclic aromatic hydrocarbons in typical urban of Yunnan-Guizhou Plateau: Characterization,sources and risk assessment

• The sampling was conducted in city on the Yunnan-Guizhou Plateau for one year. • The groups of PAHs revealed their different environmental fates and migration paths. • Seasonal biomass burning could affect the concentration by long-distance transport. • Industrial sources and traffic emissions were the main contributor of PAHs. • Living in industrial areas or winter had higher health risk by exposure PAHs in PM_2.5. Monthly particle-phase ambient samples collected at six sampling locations in Yuxi, a high-altitude city on the edge of Southeast Asia, were measured for particle-associated PAHs. As trace substances, polycyclic aromatic hydrocarbons (PAHs) are susceptible to the influences of meteorological conditions, emissions, and gas-particulate partitioning and it is challenging job to precise quantify the source and define the transmission path. The daily concentrations of total PM_2.5-bound PAHs ranged from 0.65 to 80.76 ng/m³, with an annual mean of 11.94 ng/m³. Here, we found that the concentration of PM_2.5-bound PAHs in winter was significantly higher than that in summer, which was mainly due to source and meteorology influence. The increase of fossil combustion and biomass burning in cold season became the main contributors of PAHs, while precipitation and low temperature exacerbated this difference. According to the concentration variation trend of PM_2.5-bound PAHs and their relationship with meteorological conditions, a new grouping of PAHs is applied, which suggested that PAHs have different environmental fates and migration paths. A combination of source analysis and trajectory model supported local sources from combustion of fossil fuel and vehicle exhaust contributed to the major portion on PAHs in particle, but on the Indochina Peninsula the large number of pollutants emitted by biomass burning during the fire season would affect the composition of PAHs through long-range transporting. Risk assessment in spatial and temporal variability suggested that citizens living in industrial areas were higher health risk caused by exposure the PM_2.5-bound PAHs than that in other regions, and the risk in winter was three times than in summer.     

Hydrocarbons contamination and microbial degradation in mangrove sediments of the Niger Delta region (Nigeria)

The distribution of aliphatic hydrocarbons and polycyclic aromatic hydrocarbons (PAHs), and their degradability by bacteria in epipelic and benthic sediments from Qua Iboe Estuary mangrove ecosystem and associated creeks were investigated. The research findings revealed that total aliphatic hydrocarbons in sediments ranged from 16.82 mg·kg ^?1 to 210 mg kg ^?1, wheras total PAHs ranged from 6.30 to 35.55 mg·kg ^?1 dry weight of sediment. Low molecular mass (i.e. the 2–3-ring) PAHs were predominant in almost all the sampling points, whereas the higher molecular masses (4-, 5- and 6-ring PAHs) had the lowest concentrations. In general, the sediment samples ES ₂ (39.7%), ES ₃ (24.8%), BS ₁ (46.7%), BS ₂ (49.9%) and BS ₃ (44.2%) showed<50% contributions of Σ combustion–derived PAH (COMP-PAH) concentration to the Σ PAH concentrations, whereas ES ₁ (57%) contained>50% of COMP-PAHs. Our results have also shown that many mangrove bacteria have strong capacity to utilise Qua Iboe Light (QL) crude oil as the sole source of carbon and energy, while lower number of bacterial species including Bacillus sp., Micrococcus sp., Pseudomonas aeruginosa, Alcaligenes sp. and Flavobacterium sp. exhibited detectable PAHs degradability; and as such may serve as efficient degraders of QL crude oil contamination of mangrove ecosystem.     

Distribution pattern of polycyclic aromatic hydrocarbons in particle-size fractions of coking plant soils from different depth

The concentrations of 16 priority polycyclic aromatic hydrocarbons (PAHs) in four size fractions (<2, 2–20, 20–200, >200 μm) in soils at different depth from a heavily contaminated crude benzol production facility of a coking plant were determined using GC–MS. Vertically, elevated total PAHs concentrations were observed in the soils at 3.0–4.5 m (layer B) and 6.0–7.5 m (layer C), relatively lower at 1.5–3.0 m (layer A) and 10.5–12.0 m (layer D). At all sampling sites, the silt (2–20 μm) contained the highest PAHs concentration (ranged from 726 to 2,711 mg/kg). Despite the substantial change in PAHs concentrations in soils with different particle sizes and lithologies, PAHs composition was similarly dominated by 2–3 ring species (86.5–98.3 %), including acenaphthene, fluorene, and phenanthrene. For the contribution of PAHs mass in each fraction to the bulk soil, the 20–200 μm size fraction had the greatest accumulation of PAHs in loamy sand layers at 1.0–7.5 m, increasing with depth; while in deeper sand layer at 10.5–12.0 m, the >200 μm size fraction showed highest percentages and contributed 81 % of total PAHs mass. For individual PAH distribution, the 2–3 ring PAHs were highly concentrated in the small size fraction (<2 and 2–20 μm); the 4–6 ring PAHs showed the highest concentrations in the 2–20 μm size fraction, increasing with depth. The distribution of PAHs was primarily determined by the sorption on soil organic matter and the characteristics of PAHs. This research should have significant contribution to PAH migration study and remediation design for PAHs-contaminated sites.     

Single particle analysis of ambient aerosols in Shanghai during the World Exposition, 2010: two case studies

ATSI Model 3800 aerosol time-of-flight mass spectrometer (ATOFMS) was deployed for single-particle analysis in Shanghai during the World Exposition (EXPO), 2010. Measurements on two extreme cases: polluted day (1st May) and clean day (25th September) were compared to show how meteorological conditions affected the concentration and composition of ambient aerosols. Mass spectra of 90496 and 50407 particles were analyzed respectively during the two sampling periods. The ART-2a neural network algorithm was applied to sort the collected particles. Seven major classes of particles were obtained: dust, sea salt, industrial, biomass burning, organic carbon (OC), elementary carbon (EC), and NH₄-rich particles. Number concentration of ambient aerosols showed a strong anti-correlation with the boundary layer height variation. The external mixing states of aerosols were quite different during two sampling periods because of different air parcel trajectories. Number fraction of biomass burning particles (43.3%) during polluted episode was much higher than that (21.6%) of clean time. Air parcels from the East China Sea on clean day diluted local pollutant concentration and increased the portion of sea salt particle dramatically (13.3%). The large contribution of biomass burning particles in both cases might be an indication of a constant regional background of biomass burning emission. Mass spectrum analysis showed that chemical compositions and internal mixing states of almost all the particle types were more complicate during polluted episode compared with those observed in clean time. Strong nitrate signals in the mass spectra suggested that most of the particles collected on polluted day had gone through some aging processes before reaching the sampling site.     

Evidence for covalently bonded chlorine–fullerene formed by ozonation and chlorination at room temperature

This article reports for the first time that fullerene (nC₆₀) can form chlorinated disinfection by-products in aqueous systems at ambient temperature. The ability of nC₆₀ to form colloidal suspensions in aqueous media increases the chance that these particles will migrate in the environment and then in drinking water supply systems. Since nC₆₀ is not completely removed by conventional water treatment, any residual nC₆₀ is likely to be oxidized during disinfection process. While the ozonation of nC₆₀ has been studied, little is known about the reaction between nC₆₀ and chlorine. To address this issue, we subjected aqueous nC₆₀ suspensions to chlorination and sequential ozonation/chlorination at ozone dosages of 4.5, 10, 15 and 24 mg O₃/mg nC₆₀. The morphology and physicochemical properties of oxidized nC₆₀ aggregates were evaluated by scanning electron microscopy, transmission electron microscopy, UV–visible absorption spectroscopy and X-ray photoelectron spectroscopy (XPS). We found that while the particles in the as-prepared nC₆₀ were predominantly spheres, the ozonation of nC₆₀ resulted in the formation of irregularly shaped aggregates. The concentration of atomic carbon found by XPS in the nC₆₀ samples decreased from 92 % for the as-prepared nC₆₀ to 50 % for the aggregates ozonated at 24 mg O₃/mg nC₆₀ and then chlorinated at 68 mg Cl₂/L and allowed to react for 100 min. The presence of Cl atoms covalently bonded to C atoms was confirmed by XPS peaks corresponding to a binding energy (E _b) of 200.1–202.4 eV. This demonstrates the need to better assess and monitor the formation of potentially toxic chlorinated disinfection by-products from carbon nanomaterials during water treatment.     

Oyster shell reduces PAHs and particulate matter from incense burning

This is the first report showing reduction of particle matter and PAHs from incense burning by addition of oyster shell. Worshiping ancestors and gods by burning incense sticks and joss paper is a very important tradition in many Asian regions. More than 45 % of families in Taiwan burn incense twice a day. Unlike joss paper burning, most of the incense burning occurs indoors, thus creating a risk for human health. Previous reports have indeed evidenced toxicity of incense, notably due to particulate matter and polycyclic aromatic hydrocarbons (PAHs). However, there are few methods to reduce particle matter and PAHs from incense burning. We hypothesize that oyster shell may be used to reduce incense fumes toxicity. Indeed a large amount of unused oyster shell is discarded due to increasing seafood consumption. Here, two types of incense were made in the laboratory, and then 5–30 % of oyster shells were added to the incense to study the reduction of particle matter and PAHs. Results show that reduction of particle matter and PAH emission increased with oyster shell addition. The reduction of emission factors is ?35 % for mean particle matter, ?21 % for particle-phase PAHs, and ?37 % for benzo[a]pyrene equivalent concentration (BaP_eq), using 30 % oyster shell additive. The addition of 10 % oyster shell reduces the burning time by 8.3 min, increases the burning rate by 3.4 mg/min, and reduces particle matter by 6.4 mg/g incense, particle-phase PAHs by 0.67 μg/g incense, and BaP_eq by 0.23 μg/g incense. The reductions of particle matter, particle-phase PAHs, and BaP_eq correspond to about 640 metric tons, 67, and 23 kg, respectively, per year. Our findings will help to produce safer and cleaner incense.     

Beurteilung des Ozonrisikos für die Waldregionen Bayerns am Beispiel des Jahres 2002 und des Extremtrockenjahres 2003 auf der Basis der externen Ozonexposition und der internen Ozonaufnahme

Background, aim, and scope Increasing background concentrations of ground-level tropospheric ozone and more frequent and prolonged summer drought incidences due to climate change are supposed to increase the stress on Bavarian forests. For such scenarios growth reduction and yield losses are predicted. Sustainable forest management in Bavaria aims to significantly increase the proportion of beech (Fagus sylvatica L.) because of its broad ecological amplitude. In our regional study different approaches for calculating ozone impact were used to estimate the risks for Bavarian forests in the average climatic, rather moist year 2002 and the extremely dry year 2003.Materials and methods Measurements were conducted for eleven forest ecosystem sites and two forest research sites representing typical Bavarian forest stands under different climatic conditions and situated in different altitudes. For risk assessment currently used approaches were applied either based on the calculation of the cumulative ozone exposure (external dose; MPOC maximal permitted ozone concentration; critical level AOT40_phen? accumulated ozone exposure over a threshold of 40 nl [O₃] l^–1, for the effective phenolgy of beech) or based on the calculation of the phytomedically relevant ozone flux into the stomata (internal dose, critical level AF_st>1,6, accumulated stomatal flux above a flux threshold of 1.6 nmol O₃?m^–2 PLA; PLA = projected leaf area). For calculations continuously recorded ozone concentrations and meteorological and phenological data from nearby rural open field background measuring stations from the national air pollution control and from forested sites were used. Additionally ozone induced leaf symptoms were assessed.Results The exposure-based indices AOT40_phen and MPOC as well as the flux-based index AF_st>1.6suggest that Bavarian forests are at risk from O₃ during a rather moist average year concerning climate conditions (2002) as well as in an extreme dry year (2003). Thus, growth reductions of 5?% are predicted when thresholds are exceeded. Threshold exceedance occurred in both years at all plots, mostly already at the beginning of the growing season and often even many times over. Ozone induced leaf symptoms could be detected only on a few plots in a very slight occurrence.Discussion The results for the applied critical level indices differed depending on climatic conditions during the growing seasons: Regarding exposure-based indices, the highest degree of threshold exceedance occurred in the dry year of 2003 at all plots; the flux-based approach indicated the highest stomatal ozone uptake and thus an increased risk at moist sites or during humid years, whereas the risk was decreasing at dry sites with prolonged water limitation. Hence, soil and accordingly plant water availability was the decisive factor for the flux-modelled internal ozone uptake via stomata. Drought and increased ozone impact can generate synergistic, but also antagonistic effects for forest trees. At water limited rather dry forest sites restricted transpiration and thus production, but concurrently lower ozone uptake and reduced risk for damage can be expected.Conclusions, recommendations, and perspectives For realistic site-specific risk assessment in forest stands the determination of the internal ozone dose via modeling flux based internal stomatal ozone uptake is more appropriate than the calculation of the external ozone dose. The predicted 5?% growth reductions are in discrepancy with the frequently observed increment increase during the last decades in forest stands. Comprehensive and significant statistical verification for ozone induced forest growth reduction as well as the systematic validation of thresholds for ozone in the field is still lacking. However, a multiplicity of different specific new and retrospective growth analysis data should allow closing the gap. Moreover, the determination of canopy transpiration with sap flow measurements is a novel approach to provide cause-effect related, site specific results for the effective internal ozone dose as well as for canopy water supply and consecutively for regional risk estimation. A further future objective is the refinement of O₃ flux modelling by further consideration of soil/water budget characteristics and the above mentioned improved estimations of crown and canopy transpiration. Further, the introduction of threshold ranges for forest trees in view of their specific regional climatic conditions and their validation in real forest stands is necessary for developing meaningful ozone risk predictions for forests.     

The impact on tropospheric ozone formation on the implementation of a program for mobile emissions control: a case study in São Paulo,Brazil

The main sources of reactive hydrocarbons (RHC) and nitrogen oxides (NO_x), ozone precursors, in the Metropolitan Area of São Paulo (MASP) in the southeast of Brazil are emissions from vehicles fleets. Ambient surface ozone and particulate matter concentrations are air quality problem in the MASP. This study examined the impact that implementing a control program for mobile emissions has on ozone concentrations, An episode of high surface ozone concentrations occurring in the MASP during the March 13–15, 2000 period was used as a case study that was modeled for photochemical oxidants using the California Institute of Technology/Carnegie Mellon University three-dimensional photochemical model. Different scenarios were analyzed in relationship to the implementation of the Programa Nacional de Controle de Poluição por Veículos Automotores (PROCONVE, National Program to Control Motor Vehicle Pollution). Scenario 1 assumed that all vehicles were operating within PROCONVE guidelines. Scenarios 2 and 3 considered hypothetical situations in which the PROCONVE was not implemented. Scenario 2 set the premise that vehicles were using pre-1989 technology, whereas scenario 3 allowed for technological advances. A base case scenario, in which the official emission inventory for the year 2000 was employed, was also analyzed. The CIT model results show agreement with most measurements collected during 13–15 March 2000 modeling episode. Mean normalized bias for ozone, CO, RHC and NO _x are approximately 9.0, 6.0, ?8.3, 13.0%, respectively. Tropospheric ozone concentrations predicted for scenario 2 were higher than those predicted for scenarios 1, 3 and base case. This study makes a significant contribution to the evaluation of air quality improvement and provides data for use in evaluating the economic costs of implementing a program of motor vehicle pollution control aimed at protecting human health.     

Historical record of anthropogenic polycyclic aromatic hydrocarbons in a lake sediment from the southern Tibetan Plateau

High-altitude lake sediments can be used as natural archives to reconstruct the history of pollutants. In this work, the temporal distribution of polycyclic aromatic hydrocarbons (PAHs) was determined in a sediment core collected from the southern Tibetan Plateau (TP), which was dated by using the ²¹⁰Pb dating method and validated with the ¹³⁷Cs fallout peak. The concentrations of the anthropogenic PAHs (Σ₈PAH) in the sediment core ranged from 0.83 to 12 ng/g dw, and the fluxes of the Σ₈PAH were in the range of 2.1–27 g/cm²/year. The temporal variations in the concentration and input flux of anthropogenic PAHs were low with little variability before the 1950s, and then gradually increased from the 1950s to the 1980s, and an accelerated increase was observed after the early 1980s. The content of total organic carbon played an insignificant role in affecting the time trends of PAHs in the sediment core. Diagnostic concentration fractions of PAH components indicate PAHs in the lake sediment of the southern TP which are mainly from biomass burning and/or from long-range atmospheric transport.     

Laboratory evaluation of kinetic parameters for lake sediment denitrification models

Laboratory experiments using the acetylene blockage technique showed that denitrification rates in sediments from Lake Okeechobee, Florida, are described by Michaelis-Menten nitrate dependence and Arrhenius temperature dependence (E_act = 15.5 kcal, but do not appear to be affected by seasonal differences in the supply of carbon substrates in this eutrophic lake. Peak nitrate concentrations in the sediments are in the range of the half-saturation constant, and thus, for a given temperature, k_d varies by a factor of approximately two over the typical range of nitrate concentrations. Most diagenetic sediment denitrification models employ a single-valued rate constant k_d, to describe nitrate dependence. However, the use of a constant k_d for eutrophic lake sediments may result in a significantly erroneous estimate of annual denitrification loss.     

城市高架桥降雨径流多环芳烃（PAHs）污染特征及其生态风险评价

以上海市高架桥降雨径流作为研究对象,分析了4场高架路面降雨径流溶解相、颗粒相16种PAHs的质量浓度和场次降雨径流平均浓度（Event Mean Concentration）。探讨了城市高架降雨径流中PAHs质量浓度特征、动态变化过程和污染状况。通过对无量纲累积径流量和无量纲累积污染物负荷曲线M（V）进行幂函数拟合,对4场降雨径流不同环数和总PAHs冲刷强度进行了定量表征。以水样中8种PAHs的监测质量浓度及其对3至40种水生生物的LC50为基础数据,采用推广风险系数法对径流水体PAHs进行了生态风险评价。结果表明：地表径流中溶解态PAHs的质量浓度为27.9~979.4 ng·L-1,主要以3环和4环组分为主;颗粒态PAHs中的质量浓度为1120.1~4892.6 ng·L-1,主要以4-6环的组分为主。径流样品中PAHs更容易吸附在颗粒物上,PAHs主要以颗粒相为主,且4-6环颗粒相PAHs所占比例更高,也显示了化石燃料不完全燃烧的特征。4场降雨径流以2013-05-26次降雨EMC值最大,PAHs污染水平最高。其中通过对BaP的EMC值计算,发现4场降雨径流中BaP的EMC值皆超过了国家的排放标准,应引起相关监测管理部门重视。4场降雨径流均表现不同程度的初始冲刷效应,雨强和径流量是影响初始冲刷的2个重要因素。初始冲刷散点拟合状况良好,定量表征发现2013-06-27次降雨初始冲刷强度最大。风险商表征说明,径流水体PAHs造成的生态风险较小,但部分单体PAH对水生生物的生态影响不容忽视。     

Effects of ocean acidification, temperature and nutrient regimes on the appendicularian Oikopleura dioica: a mesocosm study

Increasing pCO₂ is hypothesized to induce shifts in plankton communities toward smaller cells, reduced carbon export rates and increased roles of gelatinous zooplankton. Appendicularians, among the most numerous pan-global “gelatinous” zooplankton, continuously produce filter-feeding houses, shortcutting marine food webs by ingesting submicron particles, and their discarded houses contribute significantly to carbon fluxes. We present a first mesocosm-scale study on the effects of temperature, pCO₂ and bloom structures on the appendicularian, Oikopleura dioica. There were effects of temperature and nutrients on phytoplankton communities. No shifts in functional phytoplankton groups, nor changes in particle sizes/morphotypes, known to impact appendicularian feeding, were observed under manipulated pCO₂ conditions. However, appendicularian abundance was positively correlated with increased pCO₂, temperature and nutrient levels, consistent with hypotheses concerning gelatinous zooplankton in future oceans. This suggests appendicularians will play more important roles in marine pelagic communities and vertical carbon transport under projected ocean acidification and elevated temperature scenarios.     

Residual levels and health risk of polycyclic aromatic hydrocarbons in freshwater fishes from Lake Small Bai-Yang-Dian, Northern China

The residual levels of polycyclic aromatic hydrocarbons (PAHs) in the liver, brain, gill and muscle tissues of four common edible freshwater fish species including crucian carp, snakehead fish, grass carp and silver carp collected from Lake Small Bai-Yang-Dian in northern China were measured by GC-MS. The distribution and composition pattern of PAHs in the fish tissues, and the effects of lipid contents in fish tissues and the octanol-water partition coefficient (Kow) of PAHs congeners on them were analyzed. The human health risk of PAHs though fish consumptions was estimated. The following results were obtained: (1) The average residual levels of total PAHs (PAH₁₆) on wet weight base in the different tissues of each fish species ranged from 4.764 to 144.254 ng/g ww. The differences in the average residual levels on wet weight base for PAH₁₆ within four fish species were not statistically significant (P > 0.05); however, these within four fish tissues were statistically significant (P < 0.01). (2) There were very similar distribution patterns of PAH congeners among both the fish tissues and the fish species, as indicated by statistically significant positive interrelationships (R = 0.58-0.97, P < 0.01 or P < 0.05). Low molecular weight (LMW) PAHs predominated the distribution in the fish tissues, accounting for 89.97% of total PAHs. Phe was the most dominant component, according for 37.79% of total PAHs, followed by Ant (18.59%), Flo (12.59%), Nap (10.79%), Fla (9.82%) and Pyr (6.43%). (3) The PAHs residues and distribution in the fish tissues are dependent on both the Kow of PAH congeners and the lipid contents in the fish tissues. There was a significant positive relationship (R = 0.7116, P < 0.0001) between lipid contents and PAHs residual levels. The statistically significant negative relationships (P < 0.05) were found between LogKow and log-transformed PAHs contents on wet weight base for all fish tissues except for the muscle tissue of snakehead fish, the brain and liver tissues of crucian carp. (4) The risk levels of total PAHs were lower than 10⁻⁵ for the muscle tissues of four studied fish species and for the brain tissues of grass carp and snakehead fish; while these were higher than 10⁻⁵ for the brain tissues of crucian carp and silver carp. The risk levels of total PAHs in the liver tissues of four studied fish species except for snakehead fish exceeded 10⁻⁵ for 2-4.5 times. However, the potency equivalent concentration (PEC) of total PAHs in four studied fish tissues were still lower than the maximum permissible BaP limits for crops and baked meat and for plants in the national criterions. The distributions of PAH congeners in fish were well simulated by a level III fugacity model, especially for low molecule weight PAHs.