Distribution and sources of polycyclic aromatic hydrocarbons in Wuhan section of the Yangtze River, China

Polycyclic aromatic hydrocarbons (PAHs) are important organic contaminants with great significance for China, where coal burning is the main source of energy. In this study, concentrations, distribution between different phases, possible sources and eco-toxicological effect of PAHs of the Yangtze River were assessed. PAHs in water, suspended particulate matters (SPM) and sediment samples at seven main river sites, 23 tributary and lake sites of the Yangtze River at the Wuhan section were analyzed. The total concentrations of PAHs in the studied area ranged from 0.242 to 6.235 μg/l in waters and from 31 to 4,812 μg/kg in sediment. The average concentration of PAHs in SPM was 4,677 μg/kg, higher than that in sediment. Benzo(a)pyrene was detected only at two stations, but the concentrations were above drinking water standard. The PAHs level of the Yangtze River was similar to that of some other rivers in China but higher than some rivers in foreign countries. There existed a positive relationship between PAHs concentrations and the TOC contents in sediment. The ratio of specific PAHs indicated that PAHs mainly came from combustion process, such as coal and wood burning. PAHs may cause potential toxic effect but will not cause acute biological effects in sedimentary environment of the Wuhan section of the Yangtze River.     

南疆棉田土壤中邻苯二甲酸酯(PAEs)的测定

采用超声萃取和柱分离技术,利用气相色谱法,对棉田环境激素类污染物质邻苯二甲酸酯进行了表层土壤(0～20 cm)分布测定.结果表明,棉田土壤中DMP、DEP、DIBP、DBP、DAP、DEHP 6种环境激素类污染物均被检出,土壤中PAEs的总含量为1 532.987 mg/kg,其中DEHP的含量最高,DIBP、DBP次...     

重庆典型岩溶区地下河水体PAEs分布特征研究

分别采集了重庆典型岩溶区5条地下河水体10个样品,用气相色谱法对样品中的邻苯二甲酸酯类(PAEs)含量进行测定,分析其在重庆典型岩溶区地下河水体中的分布特征。结果表明,常见的19种邻苯二甲酸酯类(PAEs)在重庆典型岩溶区地下河水体中均有检出,其浓度范围为103.29~2268.78μg/L;5种被美国环保局列为优先控制的PAEs类污染物中,邻苯二甲酸二丁酯(DBP)和邻苯二甲酸双(2-乙基己基)酯是主要的污染物;与国内外其他地区水体进行比较,重庆典型岩溶区地下河水体PAEs含量处于较高污染水平。     

Influence of High Levels of Total Suspended Solids on Measurement of Cod and Bod in the Yellow River, China

Using the Yellow River, China, the study explores the problem of the use of COD and BOD₅ as water quality management parameters in the presence of very high levels of suspended sediment (TSS) that characterize this river. Although the amount of natural organic matter per unit of suspended sediment of the Yellow River is not high, the very high concentration of mineral sediment in the Yellow River results in a large concentration of organic matter, which artificially inflates the laboratory values of COD and, as a consequent, leads to greatly exaggerated reports of pollution of the Yellow River. BOD₅ can more accurately reflect the pollution of the Yellow River than COD; however, measured values of BOD under-report the actual values due to settling of the sediment in the incubation chamber resulting in values that are 21.6--38.3% less than the actual values. Therefore corrections are required for laboratory COD and BOD values so that the values are not artifacts of the sediment regime. Our work provides new insight into this phenomenon and demonstrates how correction factors may be determined and used with pollution data. Our work also suggests that the actual pollution levels of the Yellow River are probably not as high as reported by monitoring agencies.     

集中式饮用水源地邻苯二甲酸酯类物质分布特征与健康风险评估

以某地区7个集中式饮用水源地为研究对象,采用固相萃取气相色谱-质谱法(SPE-GC-MS)对水体中16种邻苯二甲酸酯的分布特征和溯源进行了研究,并利用健康风险评估模型对水体PAEs进行了健康风险评价。结果表明:邻苯二甲酸二正丁酯、邻苯二甲酸二(2-乙基己基)酯、邻苯二甲酸二异丁酯和邻苯二甲酸二正辛酯在所有PAEs同系物中含量丰富,而所有样品均无邻苯二甲酸二(2-甲氧基)乙酯和邻苯二甲酸二戊酯的检出;二水厂和亨达水务断面Σ_(16)PAEs浓度最高,四水厂和五水厂断面Σ_(16)PAEs浓度最低;水体12种PAEs共提出3个主成分,揭示了91%的影响因子;层次聚类分析表明:7个采样断面聚为2类,分别代表了内河和长江水体。水体中PAEs的致癌风险值和非致癌风险值均远低于参考值,说明研究水体PAEs不会对居民构成致癌风险或其他明显的健康风险,但需加强该地区PAEs使用的规范与监管,强化末端处理,以规避风险。     

Impact of irreversible sorption of phthalate acid esters on their sediment quality criteria

The equilibrium partitioning (EqP) method has been applied to establish sediment quality criteria (SQC); however, it does not consider the nonlinear irreversible sorption of many organic contaminants. In this research, the sorption and desorption of two phthalate esters (PAEs), dimethyl phthalate (DMP) and di(2-ethylhexyl) phthalate (DEHP), in four natural sediments collected from the Yangtze River and the Yellow River were studied; the impact of irreversible sorption of DMP and DEHP on SQC has been evaluated. Based on the reversible and irreversible biphasic sorption model, the values of maximum irreversible sorption capacity (q(max)(irr)) were 125.19 μg g(-1)-337.37 μg g(-1) for DMP and 515.87 μg g(-1)-591.40 μg g(-1) for DEHP. The q(max)(irr) value was positively related to the organic carbon and black carbon contents, cation exchange capacity, and surface area of the sediments. The values of the irreversible sorption coefficient K(oc)(irr) for both DEHP and DMP in the four sediments approximated to a constant of 10(6.46 ± 0.38), which was 1-2 orders of magnitude higher than their reversible sorption coefficient K(oc)(irr). The values of SQC for PAEs based on the EqP method were modified by involving the irreversible sorption. The modified SQC of DEHP could be 2 to 20 times higher than the value predicted by the EqP method, and the assessment results for DEHP contamination in the sediments with the modified SQC were more reasonable than those with the non-modified SQC. It indicated that the current SQC based on the EqP method may be unnecessarily strict for specific organic compounds and the irreversible sorption should be taken into account.     

Natural and anthropogenic contamination of the Fratta-Gorzone river (Veneto, Italy)

Stream-bed sediment samples were collected in 2001 and 2004 along the Fratta-Gorzone River (Italy) to assess the level of heavy metal contamination. The river stretch most affected by discharges of tannery effluent showed total and pseudo-total Cr levels (up to 2,860 mg/kg) that greatly exceed national and international chemical sediment quality standards. The most contaminated section of the river bed is located downstream of the main industrial discharge. However, a large fraction of the Cr present in the sediment appears to be of lithogenic origin. At most sites, more than 50% of Cr is not soluble in aqua-regia and thus unlikely to be very mobile or easily bio-available. A negligible risk to the benthic community can be inferred for Pb, Zn, Cd, Cu and Ni. This work highlights the limitation of using existing chemical sediment quality standards alone for risk assessment. The collection and analysis of suspended solids, the determination of river discharge and of dissolved Cr at 10 field stations allowed to estimate the particulate and dissolved Cr load and to locate the river stretch that was the likely source of contaminated sediment. The pumping of dilution water from the Adige River into the Fratta-Gorzone River did not produce the expected contaminant dilution effect due to re-suspension of contaminated solid particles and the release of Cr in solution.     

Distribution patterns of nitroaromatic compounds in the water, suspended particle and sediment of the river in a long-term industrial zone (China)

Nitroaromatic compounds are known to be hazardous to ecological and human health. To assess the status of nitroaromatic compounds contamination in the main rivers in the important industrial bases of the northeastern China, we collected water, suspended particulate matter (SPM) and sediment samples from 28 sites in the Daliao River watershed and analysed them for eight nitroaromatic compounds by gas chromatography. The total concentrations of eight nitrobenzenes in the water column including aqueous and SPM phases ranged from 740 to 15,828 ng L^???1, with a mean concentration of 3,460 ng L^???1. The total concentrations of eight nitrobenzenes in the sediment were 7.47 to 8,185.76 ng g^???1, with a mean concentration of 921.98 ng g^???1, and several times higher than those found from the Yellow River in China. 4-Nitrotoluene was the predominant contaminant in the water and sediment of the three rivers of the Daliao River watershed. 2,6-Dichloro-4-nitroaniline was generally dominant in the SPM. The levels of nitroaromatic compounds were different among different sites in the Daliao River watershed, mainly caused by the distribution of pollution sources. No obvious correlation was found between the total concentrations of eight nitrobenzenes concentrations and TOC or the slit-clay content of the sediments.     

Metal Pollution Assessment of Sediment and Water in the River Hindon, India

The metal pollution in water and sediment of the River Hindon in western Uttar Pradesh (India) was assessed for Cd, Cr, Cu, Fe, Mn, Ni, Pb and Zn. The metal concentrations in water showed wide temporal variation compared with bed sediment because of variability in water discharge and variations in suspended solid loadings. Metal concentrations in bed sediments provided a better evaluation of the degree and the extent of contamination in the aquatic environment, Santagarh and Atali being the most polluted sites of the river. The ratio of heavy metals to conservative elements (Fe, Al, etc.) may reveal the geochemical imbalances due to the elevated metal concentrations normally attributed to anthropogenic sources. Metal/Al ratios for the bed sediments of the river Hindon were used to determine the relative mobility and general trend of relative mobility occurred Fe > Mn > Zn > Cr > Ni > Pb > Cu > Cd.     

Distribution and contamination assessment of heavy metals in sediment of the Second Songhua River, China

The Second Songhua River was subjected to a large amount of raw or primary effluent from chemical industries in Jilin city in 1960s to 1970s, resulting in serious mercury pollution. However, an understanding of other trace metal pollution has remained unclear. The objective of this study was to investigate trace metal contamination in the sediment of the river. Bottom sediment samples were taken in the river between Jilin city and Haerbin city in 2005. An uncontaminated sediment profile was taken in the Nen River at the same time. Total concentrations of Al, Fe, Mg, Ca, K, Na, Ti, Mn, V, Sc, Co, Cu, Cr, Ni, Pb and Zn in the sediment samples were measured by ICP-MS or ICP-OES, following digestion with various acids. Concentrations of Co, Cu, Cr, Ni, Pb and Zn in the surface sediments were 5.1–14.7, 18.5–78.9, 2.4–75.4, 7.2–29.0, 13.5–124.4, and 21.8–403.1 mg/kg, respectively, generally decreasing along the course of the river from Jilin city to Haerbin city. Background concentrations of trace metals were reconstructed by geochemical normalization to a conservative element scandium. Results showed that concentrations of Co, Cr, and Ni in the sediment were generally only slightly higher than or equal to their background values, while concentrations of Cu, Pb, and Zn in the some sediment samples were significantly higher than their background values. In detail, the sediment at Jilin city was moderately contaminated by Cu, and the sediment of the Second Songhua River was moderately contaminated by Pb and Zn. The top layer (0–10 cm depth) and bottom layers (30–46 cm depth) of one sediment profile at Wukeshu town were generally moderately polluted by Pb and Zn. Synthetically, the surface sediment in the studied river section was classified as natural sediment without ecological risk by the sediment pollution index (SPI) of Cu, Cr, Ni, Pb and Zn. Only the 30–45 cm depth of the sediment profile at Wukeshu town was classified as low polluted sediment by the SPI of these metals, recording a historical contamination of the river in the 1960s to 1970s. This buried contamination of trace metals might pose a potential risk to water column under disturbance of sediment. Foundation item: The National Basic Research Priorities Program of China (2004CB418502)     

西安市表层土壤中邻苯二甲酸酯(PAEs)含量与构成

通过在西安市三环内6个功能区布设62个采样点,采样分析其表层土壤中邻苯二甲酸酯(PAEs)质量比及其构成特征。结果表明,西安市表层土壤中DMP、DEP、BBP、DnBP、DEHP和DnOP平均值分别为0.188 mg/kg、0.187 mg/kg、0.091 mg/kg、4.174 mg/kg、6.122 mg/kg和0.188 mg/kg,6种PAEs总质量比(∑6PAEs)范围为1.54 mg/kg^153.17 mg/kg,平均值为10.95 mg/kg。6个功能区∑6PAEs从高到低为交通区>工业区>混合区>公园>文教区>住宅区。与其他城市表层土壤中PAEs值比较发现,DMP处于高水平,DEP、DnBP、DEHP和∑6 PAEs处于较高水平,BBP和DnOP处于中等水平。     

Spatial and temporal variation in suspended sediment, organic matter, and turbidity in a Minnesota prairie river: implications for TMDLs

The Minnesota River Basin (MRB), situated in the prairie pothole region of the Upper Midwest, contributes excessive sediment and nutrient loads to the Upper Mississippi River. Over 330 stream channels in the MRB are listed as impaired by the Minnesota Pollution Control Agency, with turbidity levels exceeding water quality standards in much of the basin. Addressing turbidity impairment requires an understanding of pollutant sources that drive turbidity, which was the focus of this study. Suspended volatile solids (SVS), total suspended solids (TSS), and turbidity were measured over two sampling seasons at ten monitoring stations in Elm Creek, a turbidity impaired tributary in the MRB. Turbidity levels exceeded the Minnesota standard of 25 nephelometric units in 73% of Elm Creek samples. Turbidity and TSS were correlated (r ²?=?0.76), yet they varied with discharge and season. High levels of turbidity occurred during periods of high stream flow (May–June) because of excessive suspended inorganic sediment from watershed runoff, stream bank, and channel contributions. Both turbidity and TSS increased exponentially downstream with increasing stream power, bank height, and bluff erosion. However, organic matter discharged from wetlands and eutrophic lakes elevated SVS levels and stream turbidity in late summer when flows were low. SVS concentrations reached maxima at lake outlets (50 mg/l) in August. Relying on turbidity measurements alone fails to identify the cause of water quality impairment whether from suspended inorganic sediment or organic matter. Therefore, developing mitigation measures requires monitoring of both TSS and SVS from upstream to downstream reaches.     

Distribution of heavy metals in water, particulate matter and sediments of Gediz River (Eastern Aegean)

The present paper is the first document of heavy metal levels in surficial sediment, water and particulate matter of the Gediz River collected from five different sites in August, October 1998, February, June 1999. The present work attempts to establish the status of distribution and environmental implications of metals in the sediment, water and particulate matter and their possible sources of derivation. The concentrations of mercury ranged 0.037–0.81, 120–430; lead 0.59–1.5, 190–8,100; copper 0.24–1.6, 30–180; zinc 0.19–2.9, 10–80; manganese 30–170, 20–490; nickel 0.39–9.0, 100–510; iron 1.3–687, 100–6,200 μg/l in water and particulate matter, respectively. The maximum values in water were generally obtained in summer periods due to industrial and agricultural activities at Muradiye. The particulate metal concentrations also generally showed increased levels from the upper Gediz to the mouth of the river. Calculation of metal partition coefficients shows that the relative importance of the particulate and the water phases varies in response to water hydrochemistry and suspended solid content, but that most elements achieve a conditional equilibrium in the Gediz River. The metals ranged between Hg: 0.25–0.49, Cr: 59–814, Pb: 38–198, Cu: 15–148, Zn: 34–196, Mn: 235–1,371, Ni: 35–175, and Fe: 10,629–72,387 mg/kg in sediment. The significant increase of metals found in Muradiye suggested a pollution effect, related to anthropogenic wastes. Also, relatively high concentrations of Ni and Mn occurred in sampling site upstream, due to geochemical composition of the sediments. Maximum values of contamination factor for metals were noticed for sediment of Muradiye. The sampling stations have very high degree of contamination indicating serious anthropogenic pollution.     

贵州省部分地区土壤中酞酸酯类污染现状调查

对贵州省部分地区表层土壤中酞酸酯类的污染状况进行了调查。分别在遵义地区、黔南地区、黔东南地区和毕节地区采集483个土壤样品分析,结果表明,样品中酞酸酯总质量比(ΣPAEs)为未检出~8.22 mg/kg,均值为0.63 mg/kg。其中DEHP和DBP为主要污染物,均值分别为0.32 mg/kg和0.24 mg/kg,检出率分别为90.89%和97.10%。     

Behavior of di(2-ethylhexyl) phthalate discharged from domestic waste water into aquatic environment

The behavior of di(2-ethylhexyl) phthalate (DEHP) discharged from domestic waste water into river water, sediment and submerged aquatic vegetation was investigated. The concentrations of DEHP were found to be between 8-25 microg L(-1) in river water, 1,000-2,000 microg kg(-1) in sediment and less than 20-2,000 microg kg(-1) in submerged aquatic vegetation. The experiments performed in laboratory were on the biodegradation of DEHP in water and sediment, and also adsorption equilibrium of DEHP between water and sediment. The results obtained from the investigations made it clear that the high enrichment of DEHP from water to sediment was caused from not only its high adsorptive potential but also slow degradation in sediment.     

Assessment of the exposure of two fish species to metals pollution in the Ogun river catchments, Ketu, Lagos, Nigeria

The concentrations of metals (Ca, Cd, Fe, Mn, Pb and Zn) were determined by flame atomic absorption spectrophotometry in water, sediments and fish samples in the Ogun river catchments, Ketu, Lagos, which is an important bird nesting, fishing and drinking water source. The results show that the southern tip bothering the Lagos lagoon is where the highest metal concentrations are found in the fish species (Tilapia sp. and Chrysichthys sp.), whereas the Agboyi creek segment near the lagoon with higher surrounding human population density recorded higher levels of metals in sediments and water samples. The two fish species accumulated different amounts of metals. However, the differences were not statistically different at p < 0.05. There is a significant correlation (p < 0.05) for Cd concentration in water. The concentrations of Pb in sampling points 3 and 4 as well as Cd, Mn and Fe in all six sampling points exceeds the World Health Organization (WHO) limits for drinking water. Levels of metals obtained for sediments are within the range reported for Nigeria’s river sediments. Based on this study, the human risks for heavy metals in the harvested fish species from the Ogun river catchments, Ketu, are low for now as the concentrations were below the recommended Food and Agriculture Organization (FAO) maximum limits for Pb (0.5 mg/Kg), Cd (0.5 mg/Kg), and Zn (30 mg/Kg) in fish.     

Distributions of phthalic esters carried by total suspended particulates in Nanjing, China

Atmospheric trace phthalic esters (PAEs) carried by total suspended particulates were systematically investigated. A total of 450 air samples were collected at six typical locations and three specific micro-environmental sites (a stadium with a new plastic track, new cars, and a farming greenhouse with plastic film) in Nanjing metropolitan area of China from April 2009 to January 2010. The samples were analyzed by high-performance liquid chromatography and ultraviolet detection. The results are summarized as follows: (1) The dominant PAEs are dimethyl phthalate (DMP), dibutyl phthalate (DBP), and diethylhexyl phthalate (DEHP), which were found in the atmosphere of Nanjing. The average concentrations of DMP, DBP, and DEHP were 10.5?±?1.2, 62.3?±?4.5, and 33.3?±?2.5?ng?m(-3), respectively, constituting 9.9%, 58.7%, and 31.4% of total PAEs (106?±?8.2?ng?m(-3)). (2) The dynamic variations of atmospheric PAEs in the three specific micro-environmental sites showed that the PAE concentrations in the stadium with a new plastic track reduced to normal after 1?month remediation, while new cars need 6?months to remove their effect. The levels of PAEs in a farming greenhouse with plastic film were relatively high, but little PAEs accumulated in vegetables. (3) The vertical profiles from 1.5 to 40?m above ground display some fluctuations in PAE concentration, but no significant height dependence. This information will make a valuable contribution to the examination of the influence of atmospheric PAEs on the environment and human health.     

Characteristics of and Human Influences on Nitrogen Contamination in Yellow River System, China

Nitrogen (N) contamination in the Yellow River mainstream and its tributaries was studied using data from 1960 to 2000 from 312 monitoring sites in the Yellow River system. Data showed that N concentrations in the Yellow River have increased since 1960, especially after 1990. N concentrations in the Yellow River mainstream increased from the upper reaches (less than 1.0 mg L(-1) for TN and less than 0.10 mg L(-1) for NH4(+)-N) to lower reaches (higher than 4-5 mg L(-1) for TN and higher than 1.0 mg L(-1) for NH4(+)-N). However, the highest N contaminations (50-250 mg L(-1) for TN and 10-20 mg L(-1) for NH4(+)-N) was found in some tributaries, which was attributed as an effect of industrial wastewater and municipal sewage. Nitrogen concentrations from several monitoring sites were positively correlated with several regional socio-economic indices, such as population density, fertilization rates, livestock, industrial input and GDP. Depending on location, seasonal N concentrations contrasted among watersheds. Monitoring stations located in rural and agricultural areas showed higher N concentrations during the flood season while those located in areas with urban and industrial centers showed higher N concentration during the dry season. Mainstream flow and N concentrations showed a strong inverse relationship; with higher N concentrations as the river flow declined. Intensive water extraction for agricultural irrigation and increasing N input to the river from fertilized agricultural fields could explain the increasing N concentrations during extensive droughts.     

Mineral compositions and sources of the riverbed sediment in the desert channel of Yellow River

The Yellow River flows through an extensive, aeolian desert area and extends from Xiaheyan, Ningxia Province, to Toudaoguai, Inner Mongolia Province, with a total length of 1,000 km. Due to the construction and operation of large reservoirs in the upstream of the Yellow River, most water and sediment from upstream were stored in these reservoirs, which leads to the declining flow in the desert channel that has no capability to scour large amount of input of desert sands from the desert regions. By analyzing and comparing the spatial distribution of weight percent of mineral compositions between sediment sources and riverbed sediment of the main tributaries and the desert channel of the Yellow River, we concluded that the coarse sediment deposited in the desert channel of the Yellow River were mostly controlled by the local sediment sources. The analyzed results of the Quartz-Feldspar-Mica (QFM) triangular diagram and the R-factor models of the coarse sediment in the Gansu reach and the desert channel of the Yellow River further confirm that the Ningxia Hedong desert and the Inner Mongolian Wulanbuhe and Kubuqi deserts are the main provenances of the coarse sediment in the desert channel of the Yellow River. Due to the higher fluidity of the fine sediment, they are mainly contributed by the local sediment sources and the tributaries that originated from the loess area of the upper reach of the Yellow River.     

Heavy Metal Transport and Behavior in the Lower Columbia river, USA

The primary objective of this study was to evaluate temporal changes in heavy metal content of lower Columbia River sediment following terminated or reduced soluble heavy metal loading from the world's largest lead-zinc refinery and mining districts in the USA and Canada. Sediment cores were collected from two fine sediment depositional sites (∼600 km downstream) in August 1999 and were analyzed for total metal content, texture, and age/dating parameters. Zinc, cadmium and lead contents in 1999 declined by only a factor of two over their depth profile maxima (dated as between 1970 and 1980). In sharp contrast, more than a 10-fold decrease in dissolved metal loading occurred during this same period. Zinc in filtered Columbia River water at downstream locations also declined by > 10-fold, consistent with the reduced upper river solute-metal loading. Once soluble metal releases are reduced or terminated, the solute half-time in Columbia River water is months versus ∼20 yr for adsorbed metals on surficial (or resuspended) bed sediments. The much slower rate of decline for sediment, as compared to the solute phase, is attributed to resuspension, transport and redeposition of irreversibly bound metals from upstream sedimentary deposits. This implies downstream exposure of benthic or particle-ingesting biota can continue for years following source remediation and/or termination of soluble metal releases. Accordingly, contaminant contents of both particulate and solute phases of river water, as well as sediment core sections, are suggested for assessing long-term biotic exposure/response to mitigation activities in the Columbia River and similar fluvial ecosystems.