Evaluation of biogenic and anthropogenic inputs of aliphatic hydrocarbons to Lake Taihu sediments using biomarkers

Surficial sediments from 13 sites throughout Lake Taihu, one of the largest urbanized freshwater lake systems in China, were analyzed for biomarkers (e.g., n-alkanes and hopanes) to track the origin of organic inputs (biogenic or anthropogenic), and, thus, to identify any ‘hot spots’ of hydrocarbon contamination. A distinct spatial distribution of aliphatic hydrocarbons in sediments was observed in Lake Taihu. At the northern tip of the lake (i.e., Meiliang and Wuli Bays), the highest mean aliphatic hydrocarbon concentration, with a significant contribution of an unresolved complex mixture (UCM), was found, indicating possible anthropogenic petroleum contamination (mainly from untreated and partially treated industrial and domestic sewage from Wuxi, Changzhou and other cities). This was supported by the n-alkane indices (e.g., small Carbon Preference Index and odd-to-even values) and a high degree of maturity of the hopane biomarkers. However, hydrocarbons from East Taihu were mainly biogenic, with the lowest mean concentrations, negligible or no contribution of UCM, abundance of vascular plant C₂₃–C₃₃ n-alkanes with a high odd-to-even predominance, and the presence of biogenic hopanes (e.g., 17β(H), 21β(H)-hopanes and hopenes). In the other areas of the lake, however, the predominance of biogenic in combination with petrogenic hydrocarbons was indicated by the biomarkers.     

The impact of petroleum hydrocarbons (diesel) on periphyton in an impacted tropical estuary based on in situ microcosms

The distribution of petroleum hydrocarbons and their effects on the periphytic algal biomass using in situ microcosms were investigated in Ponggol estuary located on the northeastern coast of Singapore. Dissolved or dispersed petroleum hydrocarbon (DDPH) concentrations in the surface and bottom waters and absorbed or adsorbed petroleum hydrocarbon (AAPH) concentrations in sediments were monitored from July 1999 to June 2000. Results showed concentrations ranging from 4.42 to 248.94 μg l⁻¹, from 0.35 to 1099.65 μg l⁻¹, and from 20.55 to 541.01 mg kg⁻¹ for DDPH in surface and bottom waters and AAPH in sediments, respectively. Accidental spillages of fuel from dredgers operating in the estuary, fuel and engine oil from recreational boats, shipping operations in the adjacent strait, and runoff monsoon drains in the vicinity were some of the possible sources of petroleum hydrocarbons in the estuary. An assessment of environmentally realistic concentrations of petroleum hydrocarbons on periphytic algal biomass using in situ microcosms revealed signs of acute toxicity. A reduction in periphytic algal biomass (with respect to controls) of 68-93% was observed for various treatments exposed to diesel.     

Characterization of 2T engine oil degrading indigenous bacteria,isolated from high altitude (Mussoorie), India

The biodegradability of petroleum hydrocarbons such as polycyclic aromatic hydrocarbons (PAHs) and n-branched alkanes etc. of 2T engine oil were studied in aqueous media using bacterial strain isolated from petroleum contaminated soil of high altitude. Out of five petroleum degrading bacterial strain one of the most growing bacteria was identified as Enterobacter strain by morphological, physiological, biochemical and partial sequencing of 16S rDNA. This strain was capable of degrading 75 ± 3% of n-alkanes, 32 ± 5% PAHs, and the abiotic loss was 24 ± 6% during 10 days incubation period. 85 ± 2% of n-alkanes and 51 ± 3% PAHs were biodegraded in 20 days. The abiotic loss during this period was 15 ± 3%. In 30 days of incubation period 98% ± 1% n-alkanes and 75 ± 3% PAHs were degraded. As expected abiotic losses were smaller with increasing long chain alkanes and PAH’s concentration. An increment in oil degradation was correlated to an increase in cell number indicating that the bacterial isolate was responsible for the oil degradation. The hydrocarbon contents were measured by Shimadzu QP-2000 Gas chromatography/mass spectrometry by ULBON HR-1 column.     

On polynuclear aromatic hydrocarbons contamination levels in the ecosystem of Lake Peipsi in the 1970s–1980s

The data on benzo(a)pyrene (BaP) and other polynuclear aromatic hydrocarbons (PAH) pollution of Lake Peipsi and its tributaries in the 1970s–1980s have been summarized. Systematic data on the pollution of Lake Peipsi by BaP are available. The BaP content in lake water varied from <0.1 to 237 ng 1^–1. The content and qualitative composition of PAH varied in different observations. PAH were accumulated mainly in the bottom sediments; in their surface layer BaP concentrations were 10³–10⁶ times higher than in water. The concentration of the PAH in bottom sediments varied from 16 to 580 µg kg^–1 in the lake and from 40 to 2800 µg kg^–1 in its tributaries. The content of BaP in fish and biota was not high. Among the pollution sources the atmospheric pollution played quite a significant role. The lake was also polluted by oil spillage and fuel exhausts from boats and ships. The PAH concentration in the water of the tributaries was somewhat higher than in the area of Lake Peipsi.     

Hydrocarbon degradation potential of salt marsh plant–microorganisms associations

Estuaries are often considered sinks for contaminants and the cleanup of salt marshes, sensitive ecosystems with a major ecological role, should be carried out by means of least intrusive approaches, such as bioremediation. This study was designed to evaluate the influence of plant–microorganisms associations on petroleum hydrocarbons fate in salt marshes of a temperate estuary (Lima River, NW Portugal). Sediments un-colonized and colonized (rhizosediments) by different plants (Juncus maritimus, Phragmites australis, Triglochin striata and Spartina patens) were sampled in four sites of the lower and middle estuary for hydrocarbon degrading microorganisms (HD), total cell counts (TCC) and total petroleum hydrocarbons (TPHs) assessment. In general, TPHs, HD and TCC were significantly higher (P < 0.05) in rhizosediments than in un-colonized sediments. Also recorded were differences on the abundance of hydrocarbon degraders among the rhizosediment of the different plants collected at the same site (J. maritimus < P. australis < T. striata), with statistically significant differences (P < 0.05) between J. maritimus and T. striata. Moreover, strong positive correlations—0.81 and 0.84 (P < 0.05), between biotic (HD) and abiotic (organic matter content) parameters and TPHs concentrations were also found. Our data clearly suggest that salt marsh plants can influence the microbial community, by fostering the development of hydrocarbon-degrading microbial populations in its rhizosphere, an effect observed for all plants. This effect, combined with the plant capability to retain hydrocarbons around the roots, points out that salt marsh plant–microorganisms associations may actively contribute to hydrocarbon removal and degradation in estuarine environments.     

Hydrocarbon accumulation in freshwater sediments of an urban catchment

The top and bottom of two sediment cores collected from an urban receiving basin in NW London, and stormwater samples from the attendant catchment, have been analysed for their hydrocarbon content. In surface sediments, basal sediments and stormwater, total aliphatic hydrocarbon levels are 445–690 μg g⁻¹ dry wt., 43–224 μg g⁻¹ and 0.36–1.10 mg l⁻¹, respectively; and total levels of polyaromatic hydrocarbons (PAHs) are 780–1 100 μg g⁻¹, 310–640 μg g¹ and 5.83–18.21 mg l⁻¹, respectively. Biodegradation of aliphatics is assessed by phytane:n-C₁₈ and pristane: n-C₁₇ ratios. Hydrocarbon sources are determined from phytane: pristane ratios, odd: even carbon chain length ratios, the presence of an unresolved complex mixture, and by comparison of the amount of methyl-substituted PAH s with that of the parent compounds. Comparison of total levels between surface and basal sediments shows a 1 to 3 fold increase in total PAHs and a 3 to 10 fold increase in aliphatic hydrocarbons over a 120 year period.     

Differences in Sediment Organic Matter Composition and PAH Weathering between Non-Vegetated and Recently Vegetated Fuel Oiled Sediments

We examined polycyclic aromatic hydrocarbon (PAH) attenuation in contaminated field sediments after only 2 years of plant growth. We collected sediments from vegetated and non-vegetated areas at the Indiana Harbor Canal (IHC), an industrialized area with historic petroleum contamination of soils and sediments. PAH concentrations, PAH weathering indices, and organic matter composition in sediments colonized by Phragmites, cattails, or willow trees were compared to the same indices for non-vegetated sediments. We hypothesized that bulk sediment and humin fractions with measurable increases in plant organic matter content would show measurable changes to PAH attenuation as indicated by more weathered PAH diagnostic ratios or reduced PAH concentrations. Carbon-normalized PAH concentrations were lower in vegetated bulk sediments but higher in vegetated humin fractions relative to non-vegetated sediment fractions. Total organic carbon content was not indicative of more weathered N₃/P₂ ratios or reduced PAH concentrations in vegetated sediment fractions. More weathered N₃/P₂ ratios were observed with increased modern carbon (plant carbon) content of vegetated sediment fractions. Phragmites sediments contained more modern carbon (plant carbon) and more weathered PAH ratios [C₃-naphthalenes and C₂-phenanthrenes (N₃/P₂)] than willow, cattail, and non-vegetated sediments.     

Metagenomic analysis of microbial communities across a transect from low to highly hydrocarbon-contaminated soils in King George Island,Maritime Antarctica

Soil samples from a transect from low to highly hydrocarbon-contaminated soils were collected around the Brazilian Antarctic Station Comandante Ferraz (EACF), located at King George Island, Antarctica. Quantitative PCR (qPCR) analysis of bacterial 16S rRNA genes, 16S rRNA gene (iTag), and shotgun metagenomic sequencing were used to characterize microbial community structure and the potential for petroleum degradation by indigenous microbes. Hydrocarbon contamination did not affect bacterial abundance in EACF soils (bacterial 16S rRNA gene qPCR). However, analysis of 16S rRNA gene sequences revealed a successive change in the microbial community along the pollution gradient. Microbial richness and diversity decreased with the increase of hydrocarbon concentration in EACF soils. The abundance of Cytophaga, Methyloversatilis, Polaromonas, and Williamsia was positively correlated (p-value = <.05) with the concentration of total petroleum hydrocarbons (TPH) and/or polycyclic aromatic hydrocarbons (PAH). Annotation of metagenomic data revealed that the most abundant hydrocarbon degradation pathway in EACF soils was related to alkyl derivative-PAH degradation (mainly methylnaphthalenes) via the CYP450 enzyme family. The abundance of genes related to nitrogen fixation increased in EACF soils as the concentration of hydrocarbons increased. The results obtained here are valuable for the future of bioremediation of petroleum hydrocarbon-contaminated soils in polar environments.     

Distribution and Association Form of Polynuclear Aromatic Hydrocarbons in Sediments from Tokyo Bay

Polynuclear aromatic hydrocarbons (PAH), including fluoranthene, pyrene, benzo(a)-anthracene, chrysene, benzo(a)pyrene (benzo(e)pyrene), dibenzo(a,h)anthracene and benzo(ghi)perylene, were identified and determined in sediments from Tokyo Bay. Their concentrations were proved to be in a range from several tens to several hundreds µg/kg of dry samples. This seems to suggest that the smaller are the average particle sizes of sediments and the higher are the total amounts of PAH concentrations.

Statistically significant positive correlations were observed between the following pairs: total amount of PAH vs. clay content; total amount of PAH vs. the sum of (clay + silt) contents; total amount of PAH vs. ignition loss. In addition, significant positive correlations were statistically found between ignition loss and clay content as well as the sum of (clay + silt) contents.     

Distribution, sources and potential toxicological significance of polycyclic aromatic hydrocarbons (PAHs) in Taihu Lake sediments, China

Taihu Lake is one of the largest freshwater lakes in China. The lake is very shallow with a mean depth of 1.9 m and an area of 2428 km². This is the first time that polycyclic aromatic hydrocarbon concentrations in the surface sediments of Taihu Lake have been analyzed. A distinctive spatial distribution of PAHs was observed. Sediments from Lake Wulihu and Meiliang Bay (sites 1–5) had significantly higher PAH concentrations (858–5260 g kg^–1 dw) than any other area of Taihu Lake. These high PAH levels were associated with the input of untreated and partially treated domestic and industrial sewage from Wuxi, Changzhou, Wujin and other cities. Special PAH ratios, such as phenanthrene/anthracene and fluoranthene/pyrene, were calculated to evaluate the relative importance of different origins. The data confirmed a relatively high level of petrogenic contamination in sites 1–5 (mainly sewage discharge and the river runoff). The other samples were further from the sources of pollution and have relatively low PAH concentrations (410–768 g kg^–1 dw). The sources of PAHs in these sites (6–13) were characterized by combustion-derived PAH contamination associated with atmospheric deposition. In addition, effects range low (ERL) and effects range median (ERM) guidelines (Long et al., 1995) were used to estimate the potential of adverse effects resulting from PAH contamination in Taihu Lake sediments. The results indicated that some sites in the northern part of the lake had levels of PAH that exceeded the ERL value. This was interpreted to mean that acute biological effects may occasionally be expected to occur.     

Mycotoxins in horse feed

A total of 62 samples of commercial horse feed preparations (complementary feeds) containing cereal mixtures (“muesli” or mash, n = 39; pelleted feeds, n = 12), and plain horse feed grains (maize, n = 5; oats, n = 4; barley, n = 2) were purchased from 21 different producers/distributors from the German market. All samples were analysed by competitive enzyme immunoassays (EIA) for six different mycotoxins (mycotoxin groups). Analytes (detection limit, mean recovery) were: deoxynivalenol (DON, 10 μg/kg, 84%), zearalenone (ZEA, 5 μg/kg, 93%), fumonisin B₁ (FB₁, 2 μg/kg, 113%), T-2 toxin (T-2, 0.1 μg/kg, 71%), sum of T-2 + HT-2 toxin (T-2/HT2, 0.2 μg/kg, 97%), ochratoxin A (OTA, 0.2 μg/kg, 67%), and total ergot alkaloids (Generic Ergot Alkaloids “GEA”, 30 μg/kg, 132%). All samples contained DON (16–4,900 μg/kg, median 220 μg/kg), T-2/HT-2 (0.8–230 μg/kg, median 24 μg/kg), and T-2 (0.3–91 μg/kg, median 7 μg/kg). ZEA was detected in 98% of the samples (7–310 μg/kg, median 61 μg/kg). Most samples (94%) were positive for FB₁ (2–2,200 μg/kg, median 27 μg/kg). Ergot alkaloids were detected in 61% of samples (28–1,200 μg/kg, median 97 μg/kg), OTA was found in 42% of samples (0.2–4 μg/kg, median 0.35 μg/kg). The results demonstrate that a co-contamination with several mycotoxins is very common in commercial horse feed from the German market. The toxin concentrations were in most cases well below the levels which are usually considered as critical or even toxic. The highest mycotoxin concentrations were mostly found in single-grain cereal feed: the maximum values for DON and FB₁ were found in maize, the highest T-2/HT-2 toxin concentrations were found in oats, and the highest concentration of ergot alkaloids was found in barley. In composed feeds, no correlation between cereal composition and mycotoxin levels could be found.     

Potential of restoration and phytoremediation with Juncus roemerianus for diesel-contaminated coastal wetlands

Oil spills may considerably damage sensitive coastal wetlands. In this study, the tolerance limits of a dominant coastal salt marsh plant, Juncus roemerianus, to diesel oil and its phytoremediation effectiveness in wetland environments were investigated in the greenhouse. J. roemerianus was transplanted into salt marsh sediment contaminated with diesel fuel at concentrations of 0, 20, 40, 80, 160, 320, and 640 mg diesel g^?1 dry sediment. Plant stem density, shoot height, aboveground biomass and belowground biomass were detrimentally impacted at high oil dosages even 1 year after transplantation. Tolerance limits were estimated between 160 and 320 mg g^?1 based on various plant variables. Importantly, J. roemerianus enhanced oil degradation; at the 40 mg/g diesel dosage, concentrations of residual total petroleum hydrocarbons (TPH) in the sediment planted with J. roemerianus were significantly lower than those of unplanted sediments 1 year after treatment initiation. Furthermore, concentrations of total targeted polycyclic aromatic hydrocarbons (PAHs) and n-alkanes in the J. roemerianus planted treatment were, respectively, about 3% and 15% of the unplanted treatment. Concentration reduction in all categories of hydrocarbons suggested that J. roemerianus effectively phytoremediated the diesel-contaminated wetlands.     

Microbial communities and their ability to oxidize n-alkanes in the area of release of gas- and oil-containing fluids in Mid-Baikal (Cape Gorevoi Utes)

The microbial community in the area of oil seep in Mid-Baikal (Cape Gorevoi Utes) was studied. The number of microorganisms that oxidize normal hydrocarbons, petroleum, and easily accessible organic matter in the water mass of the lake, bottom sediments, and bitumen structures was studied in 2005?C2009. The high heterogeneity of the distribution of microorganisms associated with the deparaffination of oil in the areas of oil seeps was noted. The maximum concentrations of hydrocarbon-oxidizing microorganisms in the samples of bottom water above bitumen structures (up to 2200 ± 175 CFU/mL) and in bitumen structures themselves (up to 170 000 ± 13 000 CFU/g) were determined. A model experiment showed that in the conditions of low temperatures (4°C) the degradation of the fraction of oil n-alkanes by the natural microbial community reaches 90% over a period of 60 days.     

Biosurfactant production and hydrocarbon-degradation by halotolerant and thermotolerant Pseudomonas sp.

A hydrocarbon degrading and biosurfactant producing, strain DHT2, was isolated from oil-contaminated soil. The organism grew and produced biosurfactant when cultured in variety of substrates at salinities up to 6 g l⁻¹ and temperatures up to 45°C. It was capable of utilizing crude oil, fuels, alkanes and PAHs as carbon source across the wide range of temperature (30–45°C) and salinity (0–6%). Over the range evaluated, the salinity and temperature did not influence the degradation of hydrocarbon and biosurfactant productions. Isolate DHT2 was identified as Pseudomonas aeruginosa by analysis of 16S rRNA sequences (100% homology) and biochemical analysis. PCR and DNA hybridization studies revealed that enzymes involved in PAH metabolism were related to the naphthalene dioxygenase pathway. Observation of both tensio-active and emulsifying activities indicated that biosurfactants were produced by DHT2 during growth on both, water miscible and immiscible substrates, including PAH. The biosurfactants lowered the surface tension of medium from 54.9 to 30.2 dN/cm and formed a stable emulsion. The biosurfactant produced by the organism emulsified a range of hydrocarbons with hexadecane as best substrate and toluene was the poorest. These findings further indicate that the isolate could be useful for bioremediation and bio-refining application in petroleum industry.     

Isolation of hydrocarbon-degrading extremely halophilic archaea from an uncontaminated hypersaline pond (Camargue, France)

Little information exists about the ability of halophilic archaea present in hypersaline environments to degrade hydrocarbons. In order to identify the potential actors of hydrocarbon degradation in these environments, enrichment cultures were prepared using samples collected from a shallow crystallizer pond with no known contamination history in Camargue, France, with n-alkanes provided as source of carbon and energy. Five alkane-degrading halophilic archaeal strains were isolated: one (strain MSNC 2) was closely related to Haloarcula and three (strains MSNC 4, MSNC 14, and MSNC 16) to Haloferax. Biodegradation assays showed that depending on the strain, 32 to 95% (0.5 g/l) of heptadecane was degraded after 30 days of incubation at 40°C in 225 g/l NaCl artificial medium. One of the strains (MSNC 14) was also able to degrade phenanthrene. This work clearly shows for the first time the potential role of halophilic archaea belonging to the genera Haloarcula and Haloferax in the degradation of hydrocarbons in both pristine and hydrocarbon-contaminated hypersaline environments.     

Identification of Castasterone,Typhasterol and Teasterone from the Pollen of Zea mays

From the pollen of Zea mays, three brassinosteroids, castasterone, typhasterol and teasterone, were identified by GC/MS and/or ¹H NMR. Their concentrations in the pollen were shown by GC/SIM to be about 120 μg/kg fr.wt. (castasterone), 6.6 μg/kg fr.wt. (typhasterol) and 4.1 μg/kg fr.wt. (teasterone). It was also found that the anther contained a fairly large amount of brassinosteroids by a bioassay.     

Statistical analysis and optimization of nitrogen,phosphorus, and inoculum concentrations for the biodegradation of petroleum hydrocarbons by response surface methodology

In order to optimize and evaluate the influence of nitrogen, phosphorus, and inoculum concentrations on the biodegradation of hydrocarbon contaminated effluents, experiments based on central composite design (CCD) method were carried out for 3 days, employing C1 mixed culture and intermittent aeration. The independent variables were nitrogen concentration (X ₁), phosphorus concentration (X ₂), and inoculum concentration (X ₃) and the removal of total petroleum hydrocarbons (TPH) was the dependent variable. The optimized nutrients ratio (C:N:P = 100:20:2.7) and inoculum concentration (1.32 g/l) provided TPH removal of 71.8% after processing for three days. Analysis using gas chromatography identified five hydrocarbons classes: paraffins, isoparaffins, olefins, naphthenics, and aromatics. The naphthenic compounds did not degrade as readily as the other hydrocarbons that were identified. The following degradation percentages were obtained: 87.1% for the paraffins, 77.7% for the isoparaffins, 78.6% for the olefins, 38.4% for the naphthenics, and 71.7% for the aromatics.     

Elucidation of polycyclic aromatic hydrocarbon sources in the sinking particles in Lake Biwa, Japan

We examined monthly changes in polycyclic aromatic hydrocarbons (PAHs) in sediment trap samples collected from the northern basin of Lake Biwa, Japan, from September 2003 to July 2004 to elucidate the sources of PAHs in the lake. The most abundant concentrations were those of pyrene and fluoranthene, at μg g⁻¹ levels throughout the sampling period, with a strong positive relationship (r = 0.996, n = 10, P < 0.01). From the monthly changes in each PAH concentration and their ratios, we suspected two different sources: petroleum sources of lighter PAHs and combustion sources of middle to heavier PAHs. Because pyrene and fluoranthene decreased significantly with time during the sampling period (P < 0.05) and an abnormally high ratio of phenanthrene to anthracene was reported in September 2003, it appears that petroleum was accidentally spilled in September 2003. Although perylene was commonly found at μg g⁻¹ levels in the sediment, its concentration was comparable with those of the other PAHs in sediment trap samples. As perylene showed no significant relationship with other PAHs or other indicator molecules, we suspect that the source of perylene was different from those of other PAHs, and the perylene was mainly formed from its precursors after deposition.     

Polycyclic Aromatic Hydrocarbons in Coastal Sediment of Klang Strait,Malaysia: Distribution Pattern,Risk Assessment and Sources

Concentration, source, and ecological risk of polycyclic aromatic hydrocarbons (PAHs) were investigated in 22 stations from surface sediments in the areas of anthropogenic pollution in the Klang Strait (Malaysia). The total PAH level in the Klang Strait sediment was 994.02±918.1 µg/kg dw. The highest concentration was observed in stations near the coastline and mouth of the Klang River. These locations were dominated by high molecular weight PAHs. The results showed both pyrogenic and petrogenic sources are main sources of PAHs. Further analyses indicated that PAHs primarily originated from pyrogenic sources (coal combustion and vehicular emissions), with significant contribution from petroleum inputs. Regarding ecological risk estimation, only station 13 was moderately polluted, the rest of the stations suffered rare or slight adverse biological effects with PAH exposure in surface sediment, suggesting that PAHs are not considered as contaminants of concern in the Klang Strait.     

Background levels of polycyclic aromatic hydrocarbons (PAH) and selected metals in new England urban soils

Polycyclic aromatic hydrocarbons (PAH) are byproducts of combustion and are ubiquitous in the urban environment They are also present in industrial chemical wastes, such as coal tar, petroleum refinery sludges, waste oils and fuels, and wood‐treating residues. Thus, PAHs are chemicals of concern at many waste sites. Risk assessment methods will yield risk‐based cleanup levels for PAHs that range from 0.1 to 0.7 mg/kg. Given their universal presence in the urban environment, it is important to compare risk‐based cleanup levels with typical urban background levels before utilizing unrealistically low cleanup targets. However, little data exist on PAH levels in urban, nonindustrial soils. In this study, 60 samples of surficial soils from urban locations in three New England cities were analyzed for PAH compounds. In addition, all samples were analyzed for total petroleum hydrocarbons (TPH) and seven metals. The upper 95% confidence interval on the mean was 3 mg/kg for benzo(a)pyrene toxic equivalents, 12 mg/kg for total potentially carcinogenic PAH, and 25 mg/kg for total PAH. The upper 95% confidence interval was 373 mg/kg for TPH, which exceeds the target level of 100 mg/kg used by many state regulatory agencies. Metal concentrations were similar to published background levels for all metals except lead. The upper 95% confidence interval for lead was 737 mg/kg in Boston, 463 mg/kg in Providence, and 378 mg/kg in Springfield.