Temporal trends of hydrocarbons in sediment cores from the Pearl River Estuary and the northern South China Sea

Concentrations and fluxes of unresolved complex mixture of hydrocarbons (UCM) and polycyclic aromatic hydrocarbons (PAHs) were analyzed for two ²¹⁰Pb dated sediment cores from the Pearl River Estuary (PRE) and the adjacent northern South China Sea (NSCS). Compound-specific stable carbon isotopic compositions of individual n-alkanes were also measured for identification of the hydrocarbon sources. The historical records of PAHs in the NSCS reflected the economic development in the Pearl River Delta during the 20th century. PAHs in the NSCS predominantly derive from combustion of coal and biomass, whereas PAHs in the PRE are a mixture of petrogenic and pyrogenic in origins. The isotopic profiles reveal that the petrogenic hydrocarbons in the PRE originate predominantly from local spillage/leakage of lube oil and crude oils. The accumulation rates of pyrogenic PAHs have significantly increased, whereas UCM accumulation has slightly declined in the NSCS in the recent three decades.     

Historical trends of polychlorinated dibenzo-p-dioxins and dibenzofurans in three dated sediment cores from Mexico

This paper describes the first report of dioxins and furans (PCDDs/Fs) in sediment cores from Mexico. Sedimentation rates and vertical fluxes were estimated using ²¹⁰Pb dating. Two cores correspond to marine sediments and one to an endorheic lake. Concentrations of PCDDs/Fs found in the three sites are typical of non-impacted areas with low concentrations when compared to reference values. However the PCDDs/Fs sediment profiles show an increasing concentration trend in the upper core sections. This behavior is different from that found at many sites around the globe where diminishing concentrations have been reported. A strong predominance of OCDD was observed, and a comparison to typical composition profiles of industrial and other sources did not result in clear origin assignments for these measured compounds. We suggest that local sources may be responsible for the increase in concentration and, because these undetermined sources have not been curtailed, their importance is still growing.     

Historical record of polycyclic aromatic hydrocarbons (PAHs) and spheroidal carbonaceous particles (SCPs) in marine sediment cores from Admiralty Bay, King George Island, Antarctica

This paper describes the first results of polycyclic aromatic hydrocarbons (PAHs) and spheroidal carbonaceous particles (SCPs) in sediment cores of Admiralty Bay, Antarctica. These markers were used to assess the local input of anthropogenic materials (particulate and organic compounds) as a result of the influence of human occupation in a sub-Antarctic region and a possible long-range atmospheric transport of combustion products from sources in South America. The highest SCPs and PAHs concentrations were observed during the last 30 years, when three research stations were built in the area and industrial activities in South America increased. The concentrations of SCPs and PAHs were much lower than those of other regions in the northern hemisphere and other reported data for the southern hemisphere. The PAH isomer ratios showed that the major sources of PAHs are fossil fuels/petroleum, biomass combustion and sewage contribution generally close to the Brazilian scientific station.     

Presence of surfactants and their degradation intermediates in sediment cores and grabs from the Cadiz Bay area

The occurrence and distribution of the major surfactants--LAS, AES, APEOs and AEOs--and their degradation intermediates--SPCs, AP and APECs--in a marine-estuarine environment at Spain are presented. Results show that their concentration in surface sediments is clearly correlated with their usage and the existence of wastewater discharges. The degradation processes appear to lead to the formation of SPCs in the case of LAS, and to the shortening of the average ethoxylated chain length in the case of NPEOs, AEOs and AES. Vertical profiles for AEOs and AES are reported for the first time and present the highest values nearest the surface, followed by a sharp decrease with depth for all surfactants, as well as the appearance of degradation intermediates in deeper sedimentary layers. Shorter LAS homologues and SPCs tend to be present in pore water while strongly non-polar intermediates like NP are firmly attached to the sediments.     

Storage and distribution of trace metals and spheroidal carbonaceous particles (SCPs) from atmospheric deposition in the catchment peats of Lochnagar, Scotland.

Lochnagar is a remote mountain lake to the south-east of the Cairngorm region in Scotland. Its catchment receives anthropogenic trace metals solely from atmospheric deposition. Ten peat cores were taken from the catchment and analysis confirmed that they have been contaminated by trace metals. The peats have an high affinity for trace metals and this results in metal accumulation in the surface peat layers. The formation of trace metal sulphides may also reduce remobilisation. In this way, trace metals derived from atmospheric deposition have been scavenged and accumulated. In contaminated peat layers, 77.4% Hg, 89.6% Pb, 93.4% Cu, 72.4% Zn and 86.5% Cd of the total stored are from anthropogenic sources. The accumulated trace metals in the peats can potentially influence the lake system through erosion. Spheroidal carbonaceous particle (SCP) profiles were used to date the peat cores. By referring to the SCP profiles in the peats and comparing these with the trace metal profiles in the lake sediments, the mobility of trace metals in the catchment peats is confirmed.     

Sources and trends of trace elements and polycyclic aromatic hydrocarbons in a shallow lake in the Mediterranean area from sediment archives of the Anthropocene

Environmental Science and Pollution Research - In this study, the anthropogenic contamination in Trasimeno lake (Central Italy) was investigated using three sediment cores spanning over the last...     

2015年2月天津市大气颗粒物数浓度变化及其与气象条件的关系

2015年2月16—28日,采用APS-3321空气动力学粒径谱仪在天津市环境监测中心站连续监测0.5~10 μm间不同粒径大气颗粒物数浓度,并同步记录气象参数,研究了大气颗粒物的数浓度变化和粒径分布特征,运用Spearman统计分析方法初步探讨了气象因素对大气颗粒物数浓度的影响。结果表明,该地区大气颗粒物5 min平均数浓度为285 个·cm-3,其中0.5~1.0 μm粒径颗粒物对总粒子数浓度贡献较大,约占96.7%。观测期间共出现颗粒物数浓度显著增高的9个污染事件,不同粒径中污染事件颗粒物数浓度最大值的主导气象因素不同：对于0.5~1.0 μm,其与相对湿度呈明显的正相关性;对于1.0~2.5 μm,其与气象因素无明显相关性;对于2.5~10 μm,其与相对湿度呈明显负相关性、与风速呈明显正相关性。颗粒物数浓度受气象条件影响较大,其中相对湿度影响最为显著,当相对湿度小于70%时,颗粒物数浓度随着湿度的增加而增加;当相对湿度大于70%时,颗粒物数浓度随着湿度的增加而减少。此外,烟花爆竹燃放对颗粒物数浓度短暂上升贡献突出,主要集中在0.5~1.0 μm粒径的亚微米颗粒物。     

Metal concentrations in water,sediment and gudgeon (Gobio gobio) from a pollution gradient: relationship with fish condition factor

This study assesses the applicability of a sentinel fish species as a biomonitor of metal pollution. Gudgeon (Gobio gobio) were collected from 14 sites in metal polluted lowland rivers in Flanders, including a clear Cd and Zn pollution gradient. Fish tissues were analysed for Cd, Cr, Cu, Ni, Pb and Zn. Metal levels in organs were related to levels in water and sediment. At some sites Cd and Zn levels were up to 50 times higher compared to reference values and literature. Significant relationships between Cd and Zn in fish tissue and environmental levels were found, especially in the pollution gradient where up to 70% of the observed variation could be described. Condition factor differed significantly among the sampling sites but could not be directly related to the environmental metal levels. Nevertheless, in the pollution gradient, threshold tissue concentrations could be defined above which the condition factor was always low.     

Polybrominated diphenyl ethers (PBDEs) and their methoxylated derivatives in pike from Swedish waters with emphasis on temporal trends, 1967-2000

Temporal trends of five tetra- to hexabromodiphenyl ethers [BDE47, BDE99, BDE100, BDE153 and BDE154) and two methoxy-tetraBDEs [6-methoxy-2,2',4,4'- tetraBDE (6-MeO-BDE47) and 2'-methoxy-2,3',4,5'- tetraBDE (2'-MeO-BDE68)] in pike from Lake Bolmen for the years 1967-2000, are presented. All BDE congeners show increasing trends up to the mid-1980s (Sigma5PBDE from 60 to 1600 pg/g wet weight in 1989, i.e. a more than 25-fold increase), and then decrease or level off. The decreasing trends of PBDEs after the 1980s were considerably slower in the present study than was found in a study of an environmental matrix from the Baltic Proper covering the same time period. This difference suggests local sources near Lake Bolmen. The MeO-BDEs show initially decreasing concentrations, which for 6-MeO-BDE47 continues until the early 1990s. The concentrations of 6-MeO-BDE47 in herring from five locations along the Swedish coast increased from south to north in the Baltic Sea. No correlation between the concentrations of the BDE congeners and the MeO-BDEs was observed, indicating sources other than PBDEs for these compounds. The presence of MeO-BDEs in fish from lakes with different characteristics suggests a natural production not favoured by eutrophication, or dependent on sampling season and geographical location.