Revealing the factors affecting occurrence and distribution of polycyclic aromatic hydrocarbons in water and sediments of Lake Baikal and its tributaries

The concentrations of polycyclic aromatic hydrocarbons (PAH), total carbon (TC), total organic carbon (TOC), total nitrogen (TN) and dissolved inorganic nitrogen (DIN) in water and sediments of Lake Baikal and its tributaries were measured. It was found that according to existing water and sediment quality standards limiting permissible PAH concentrations, both surface waters and sediments in Lake Baikal watershed can be considered as unpolluted with PAHs compounds. Nevertheless, the spatial distribution of PAH concentrations in lake water indicates the existence of some point PAH sources in and around the lake. These sources were natural oil seeps and communal facilities such as residential coal-fired and oil-fired boilers. It was observed that concentrations of PAHs in both water and sediments are controlled by organic matter content and organic matter mineralisation degree, as indicated by PAH-to-carbon and nitrogen-to-carbon ratios respectively. It was found that PAH/TOC and PAH/TC ratios characterise PAH loading on water and sediments respectively, whereas DIN/TOC and TN/TC ratios characterise self-purification of water and sediments respectively. It was proved that PAH/TOC and DIN/TOC ratios can be used as tracers to evaluate the PAH contributions from tributaries to Lake Baikal.     

Inorganic and methyl-mercury speciation in sediments of the Swarzędzkie Lake

Sediment samples were analysed for mercury and methylmercury content in different parts of the bottom sediment of Swarz ?dzkie Lake, which were influenced by different external pollution sources. The results of determination with two methods of mineralization using two separate media (HNO₃/H₂O₂ and HF) were compared. The accuracy of the studied methods was analysed using certified reference material IAEA 405 of river sediment. The recovery of mercury was satisfactory and ranged from 97.5 to 98.8%. Methylmercury compounds in the studied sediments were found in limited concentrations. Their concentrations ranged from 0.26 to 58.1 μg kg^?1, i.e. 1.0–7.4% of the total mercury content. The depth profile displayed high values of both total and methylmercury content at a depth of 10–20 cm, related to the heavy pollution of the lake in the 1980s. Canonical analysis displayed the relationship of both total mercury and methylmercury concentrations with organic matter and phosphorus content in bottom sediments.     

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.     

Response of mercury accumulation to anthropogenic pollution in the past 1000 years based on Lake Huguangyan sediments,Southern China

A new ²¹⁰Pb-dated record of Hg accumulation derived from a sediment core from a Hg-enriched area in Huguangyan Lake (HGY) in South China is presented. Based on synthetic analyses of multi-proxy records including chemical composition, total organic matter, and grain-size distribution in surface sediments and nearby soil samples, it is inferred that the influx of Hg into the lake is mainly a result of atmospheric deposition, with no or minor hydroclimate-induced lithogenic input from the catchment and limited adsorption effects of organic matter and clay. Significantly enhanced anthropogenic input of Hg started in the early 1900s. Since then, several anomalies of Hg accumulation have been the results of wars or intensified economic activities in China. HGY sediments provide a rare and reliable natural archive for detecting atmospheric Hg deposition, which is closely related to anthropogenic activities.

     

Aliphatic and polycyclic aromatic hydrocarbons in the bottom sediments from Klaipėda Harbour,Lithuania (Baltic Sea)

A total of 22 bottom surface sediment samples were collected from Klaip?da Harbour, Lithuania (Baltic Sea). Sediment parameters, such as grain size and concentrations of total organic carbon, aliphatic hydrocarbons (ALHs) and polycyclic aromatic hydrocarbons (PAHs), were determined. Hydrocarbon contamination levels in the sediments were estimated based on classifications provided in the literature, and potential biological effects were assessed based on the effects range low–effects range median values of the Sediment Quality Guidelines and on the total toxic benzo(a)pyrene equivalent. The results demonstrated that concentrations of PAHs and total aliphatic hydrocarbons in the sediments varied between 1.6 and 5456?ng?g^?1 d.w. and 6.9 and 727?μg?g^?1 d.w., respectively. In most cases, the concentrations of ALHs and PAHs in the sediments indicated low to moderate levels of pollution and were not observed to have any significant adverse effects on living biota. To determine possible sources of hydrocarbons, hydrocarbon compositions were analysed, and ALHs’ and PAHs’ specific diagnostic ratios were calculated. According to the results, the Klaip?da Harbour bottom sediments were dominated by PAHs of pyrogenic origin, whereas the origin of ALHs was mixed, that is, anthropogenic with a biogenic (aquatic and terrestrial) input.     

Metal speciation in sediments of polluted and non‐polluted lakes

A five‐step extraction procedure for metal speciation studies (copper, lead, nickel, manganese and zinc) was applied to the analysis of lake sediments characterised by different environmental features. A different partition of metals into the several metal forms was observed. Both the metal fraction sorbed or co‐precipitated on hydrous Mn‐oxides (especially lead and zinc) and that bound to organic matter (especially copper) are high in some samples. A prevalently anthropogenic origin of these metals may be hypothesised on the basis of existing knowledge of the equilibrium and change phenomena occurring among water, particulate and sediments. Conversely, the non‐solubilised forms of metals are abundant in the sediments of lakes that are certainly not polluted. The concentration of manganese is very high in the sediments of Antarctic lakes; sequential extractions show its lithogenic origin. In conclusion, a knowledge of the different types of metal associations in sediments and their percentage can facilitate understanding of both natural and anthropogenic metal enrichment of aquatic systems.     

Polycyclic aromatic hydrocarbons in surface sediments held in experimental mesocosms

Sediment was collected from three locations along a pollution gradient in Narragansett Bay and transplanted to controlled mesocosms. Total hydrocarbons and eleven individual polycyclic aromatic hydrocarbons (PAHs) were measured in these sediments over a period of 394 days. Total hydrocarbon concentrations increased in the “relatively uncontaminated”; (Rhode Island Sound) sediment that was held in the mesocosms, but did not change in the two other sediments. The concentrations of four PAHs: naphthalene, 2‐methyl naphthalene, 1‐methyl naphthalene and biphenyl, decreased in the “contaminated”; (Providence River) sediment during the experiment and the calculated half‐lives for these compounds were 287, 353, 321 and 333 days, respectively.     

Hydrocarbon bioaccumulation from contaminated sediment by the deposit-feeding polychaeteAbarenicola pacifica

This study examines the role of the organic carbon content of sediment in aromatic hydrocarbon bioaccumulation and assesses the importance of two routes of hydrocarbon uptake: (1) the uptake of the particulate contaminant fraction from ingested sediment; (2) the uptake of the dissolved contaminant fraction from interstitial or overlying water. The lugwormAbarenicola pacifica was collected from San Juan Island, Washington, USA, in January 1989, and exposed to three sediments contaminated with [³H]benzo (a) pyrene (BaP). By manipulating the organic content of these sediments, it was possible to establish three treatments with similar BaP concentrations in the interstitial water, but differing in the amount of BaP in the bulk sediment. BaP bioaccumulation over the first few days of exposure was correlated with feeding rate, suggesting that ingested sediments were a source of BaP. The greatest body burden, however, was attained in those individuals held in sediments with the lowest organic carbon content and the lowest BaP concentration. Body burden at steady state was not correlated with either BaP concentrations in bulk sediment (dry weight or organic carbon-normalized bases) or the interstitial water. Increased organic matter decreased BaP bioavailability in a non-linear fashion. Bioaccumulation factors relative to water and organic content were relatively constant between 1 and 2% organic carbon in the sediment, but these same accumulation factors substantially underestimated body burden if applied to sandy sediments with little (0.3%) organic carbon.     

Methane Production in River and Lake Sediments in Taiwan

To investigate the relationship between methane production in the sediments and pollution of the river and lake, biochemical oxygen demand (BOD) and chemical oxygen demand (COD) of the water sample, organic matter content and methane production of the sediment were measured. Experimental results indicated that BOD, COD and organic matter contents were low in Bei-tan Lake, the I-lan River and reservoirs; and methane production of these sediments ranged from 0.24 to 1.06 mg L- 1. However, BOD, COD and organic matter contents were high in the Hsin-dan River, Keelung River, drainage river of Taoyuan County, park pond and fishery pond. Methane production of these sediments was between 11.75 and 54.54 mg L-1. Sediments of drain river and fishery pond had high methane production, at 25.41 to 54.54 mg methane L. Methane production of sediments had a good correlation with BOD, COD and organic matter contents. Methane production was proportional to the increment in incubation temperature from 12 to 40C.     

Spatial variation of phosphorus fractionation in the coral reef sediments of Lakshadweep Archipelago,Indian Ocean

Surface sediments were collected from the shore and lagoons of Kavaratti, Kadamat and Agatti islands of Lakshadweep Archipelago during May 2015 and analysed for the spatial distribution of the micronutrient element, phosphorus. Phosphorus was separated by sequential extraction procedure into five fractions – exchangeable (Ex-P), iron bound, (Fe-P), calcium bound (Ca-P), organic and residual fractions (OP) and total phosphorus (TP). The average relative contribution of each P species to TP was: OP?>?Ca –P?>?Ex – P?>?Fe – P. The high concentration of organic and residual phosphorus (87–96%) compared to inorganic phosphorus is particularly evident at stations characterised by higher total phosphorus concentrations. Among the three forms of IP in the sediments, Ca-P was dominant at all stations. The OC/OP ratio ranged from 3 to 163 in the sediments, suggesting that the organic matter in sediments had been subjected to degradation. Hence, the major contribution towards organic and residual phosphorus form is from the residual fraction comprising biologically resistant or non-available phosphorus form composed of refractory materials. The concentration of phosphorus reported in the present study is higher than that of the earlier studies in Lakshadweep, indicating a terrestrial and anthropogenic in?uence on the sediment.     

Metallic contaminant profiles in sediment cores from Lake Valencia,Venezuela

Total extractable concentrations of AI, Fe, Mn, Pb, Cu, Zn, Hg and organic carbon (C_org) were determined along four sediment cores from Lake Valencia. In one selected core, the percentage labile fractions were determined in order to establish anthropic enrichment factors, the depth reached by the contaminants and their mobilities. The distribution patterns of concentration versus depth reflect the original concentrations of the settling sediments. Only Mn seems to show diagenetic cycling. No enrichment of Fe and Mn occurs in the upper part of the cores, in spite of good water circulation and aeration of bottom lake waters during five months of the year. This immobility can be attributed to the high pH of water (7.6 – 8.9). Pb, Zn, Cu and Hg are enriched in the upper part of the cores, probably reflecting the input of contaminants. These elements show enrichment factors of up to 3.0. Background concentrations of the studied metals are reached below a depth of 30 cm.     

Metal distribution in marine sediments of the Mar Piccolo in Taranto (Ionic Sea,southern Italy)

The spatial distribution of selected metals (Fe, Ni, Mn, Zn, Cu, Pb, Hg and Cd) and their partition in the different chemical forms (speciation) were determined in benthic sediments from Mar Piccolo, Taranto (Ionic Sea, southern Italy). The aim of this study was to assess the degree of sediment contamination and bioavailability of metals, very important for Italian mussel culture, in a semi-enclosed marine ecosystem. In sediments, grain size distribution, total organic carbon (TOC), and humic (HA) and fulvic (FA) acids contents were also determined. The compounds TOC, HA and FA, in fact, have a great influence on metal complexation. High concentrations of copper, lead, zinc and mercury were found, especially in sediments of the first inlet of Mar Piccolo. Statistical analysis of results shows significant correlation among Cu, Pb and Zn concentrations and the influence of organic matter on the sediment distribution of Cu, Pb and Zn. Metal speciation analysis, carried out with sequential extraction method, shows that Fe and Ni are present in sediments mainly as sulphides. Mn and Pb are present principally in an ion-exchangeable form or bound to carbonate and Cu is associated to organic matter. Metal pollution index (MPI), calculated as a weighed mean of the metal contamination factors in each station, shows that with regard to Cu, Ni, Pb and Zn, some stations investigated are unpolluted (MPI <1), whereas in other areas, pollution level is not very high. On the contrary, for mercury, the pollution level in the first inlet of the basin is very high.     

Trace Organic Matter in the Ria Formosa,Portugal

The Ria Formosa lagoon, Portugal, receives organic matter from many natural and anthropogenic sources. This paper presents an overview of the contribution these sources made through the use of lipid biomarkers. Sixty-one surface sediment samples were collected and analysed for a range of lipids. Sewage materials were confined to regions within 2 km of discharge points; phytoplankton biomarkers (sterols and fatty acids) suggest production was greatest in the inner parts of the lagoon that also have greatest inorganic nutrient enrichment; terrestrial organic matter was present in relatively low concentrations as shown by both sterol and fatty alcohols; bacteria were widespread although the Sulphate Reducing Bacteria (SRBs, shown by the presence of 3-OH fatty acids) were located near but not adjacent to sewage discharge points.     

Trace Organic Matter in the Ria Formosa, Portugal

The Ria Formosa lagoon, Portugal, receives organic matter from many natural and anthropogenic sources. This paper presents an overview of the contribution these sources made through the use of lipid biomarkers. Sixty-one surface sediment samples were collected and analysed for a range of lipids. Sewage materials were confined to regions within 2 km of discharge points; phytoplankton biomarkers (sterols and fatty acids) suggest production was greatest in the inner parts of the lagoon that also have greatest inorganic nutrient enrichment; terrestrial organic matter was present in relatively low concentrations as shown by both sterol and fatty alcohols; bacteria were widespread although the Sulphate Reducing Bacteria (SRBs, shown by the presence of 3-OH fatty acids) were located near but not adjacent to sewage discharge points.     

Seasonal variation of heavy metals in sediment of Lake Ulansuhai,China

Sediment samples were collected from 10 sites in Lake Ulansuhai during summer and winter 2009 to reveal seasonal variations in sediment heavy metal levels. The geoaccumulation index (GI) was calculated to assess the severity of metal pollution. The GI values suggest that, in winter, the lake sediments were polluted slightly with Cu (GI=0.66–1.34), Zn (GI=0.59–1.35), Cr (GI=0.49–0.82) and Pb (GI=0.60–0.96), and moderately with Cd (GI=1.03–4.23). The degree of pollution was higher in winter than in summer. By contrast, the degree of pollution was higher in summer than in winter for Hg and As. Correlation analysis can be used to identify factors influencing seasonal variations in heavy metals. The concetrations of Cu, Zn, Pb, Cr and Cd were negatively correlated with water temperature and hydrodynamic conditions, but positively correlated with organic matter concentration in the sediments and with a sediment particle size of<63 μm (p<0.01). Meanwhile, Hg and As concentrations were affected by redox state and salinity. Among the metals tested, Hg and Cd posed a more serious pollution risk.     

Distribution,fractionation and risk assessment of mercury in surficial sediments of Nansi Lake,China

Nansi Lake is composed of four sub-lakes from north to south: Nanyang Lake, Dushan Lake, Zhaoyang Lake and Weishan Lake. An environmental pollution investigation was carried out to determine the fractionation, and pollution assessments of mercury (Hg) in surficial sediments from Nansi Lake. Results showed that the mean concentration of Hg was 3.1 times higher than its background value (0.015 mg kg^?1), and the high concentration of Hg which even reached up to five times than the background value in the part of Dushan Lake and Weishan Lake, which indicated that there are obvious spatial differences. The content of Hg was positively correlated with that of total organic carbon, and negatively correlated with that of pH and SiO₂ in surface sediments. An improved Tessier sequential extraction procedure was used to study the fractions of Hg in sediments. The results indicated that Hg existed primarily in the fraction of residual, which accounts for 58.4% of total mercury (THg), and the percentage of extractable Hg was only 1.93% of total mercury. High concentrations of mercury of non-residual phase were found in part lake area from the Nanyang Lake and the Weishan Lake, which indicating a higher potential ecological risk relative to the other lake areas. Based on the values of enrichment factor and geo-accumulation index, most part of Dushan Lake and Nanyang Lake and Weishan Lake were in a moderate pollution. And based on the fractionation of mercury, risk assessment code of Hg exhibited low risks to the environment in Nansi Lake.     

人为活动对城市湖泊沉积物重金属污染的影响——以武汉墨水湖为例

人类活动使得大量的重金属向水环境中排放,导致了城市湖泊严重的重金属污染.为了研究中国的工业化、城市化发展对城市水体重金属污染的影响,以武汉墨水湖为例,测定了沉积物中几种常见痕量重金属Zn、Pb、Ni、Cu、Cr的含量和富集系数,并运用主成分分析对重金属的污染来源进行了初步探讨.结果表明,墨水湖表层沉积物重金属污染程度较重,主要受人为输入的影响;5种重金属在全湖区域上具有比较高的富集系数,尤以排污口为甚,排污口是重金属富集的主要区域.主成分分析表明,Pb可能主要来自于暴雨径流面源,而Cr可能主要来自于工矿企业的点源排放,其他3种金属则有着大小相当的点、面源输入贡献。以上结果表明,城市化和工业化进程已经给城市湖泊带来了很高的重金属污染负荷.     

Assessment of persistent organic pollutants in soil and sediments from an urbanized flood plain area

Polycyclic aromatic hydrocarbons (PAHs), organochlorine pesticides (OCPs) and phenolic compounds (PCs) are persistent organic compounds. Contamination of these potentially toxic organic pollutants in soils and sediments is most studied environmental compartments. In recent past, studies were carried out on PAHs, OCPs and PCs in various soils and sediments in India. But, this is the first study on these pollutants in soils and sediments from an urbanized river flood plain area in Delhi, India. During 2018, a total of fifty-four samples including twenty-seven each of soil and sediment were collected and analyzed for thirteen priority PAHs, four OCPs and six PCs. The detected concentration of ∑PAHs, ∑OCPs and ∑PCs in soils ranged between 473 and 1132, 13 and 41, and 639 and 2112 µg/kg, respectively, while their concentrations in sediments ranged between 1685 and 4010, 4.2 and 47, and 553 and 20,983 µg/kg, respectively. PAHs with 4-aromatic rings were the dominant compounds, accounting for 51 and 76% of total PAHs in soils and sediments, respectively. The contribution of seven carcinogen PAHs (7CPAHs) in soils and sediments accounted for 43% and 61%, respectively, to ∑PAHs. Among OCPs, p, p’-DDT was the dominant compound in soils, while α-HCH was found to be dominated in sediments. The concentrations of ∑CPs (chlorophenols) were dominated over ∑NPs (nitrophenols) in both the matrices. Various diagnostic tools were applied for the identification of their possible sources in soil and sediments. The observed concentrations of PAHs, OCPs and PCs were more or less comparable with the recently reports from various locations around the world including India. Soil quality guidelines and consensus-based sediment quality guidelines were applied for the assessment of ecotoxicological health effect.

     

Chemical characteristics of fine particulate matter emitted from commercial cooking

The chemical characteristics of fine particulate matter (PM_2.5) emitted from commercial cooking were explored in this study. Three typical commercial restaurants in Shanghai, i.e., a Shanghai-style one (SHS), a Sichuan-style one (SCS) and an Italian-style one (ITS), were selected to conduct PM_2.5 sampling. Particulate organic matter (POM) was found to be the predominant contributor to cooking-related PM_2.5 mass in all the tested restaurants, with a proportion of 69.1% to 77.1%. Specifically, 80 trace organic compounds were identified and quantified by gas chromatography/mass spectrometry (GC/MS), which accounted for 3.8%–6.5% of the total PM_2.5 mass. Among the quantified organic compounds, unsaturated fatty acids had the highest concentration, followed by saturated fatty acids. Comparatively, the impacts of other kinds of organic compounds were much smaller. Oleic acid was the most abundant single species in both SCS and ITS. However, in the case of SHS, linoleic acid was the richest one. ITS produced a much larger mass fraction of most organic species in POM than the two Chinese cooking styles except for monosaccharide anhydrides and sterols. The results of this study could be utilized to explore the contribution of cooking emissions to PM_2.5 pollution and to develop the emission inventory of PM_2.5 from cooking, which could then help the policymakers design efficient treatment measures and control strategies on cooking emissions in the future.