Pre- and post-industrial levels of polycyclic aromatic hydrocarbons in sediments from the Estuary and Gulf of St. Lawrence (eastern Canada).

The concentrations of 23 polycyclic aromatic hydrocarbons (PAHs; 16 parent PAHs and 7 alkyl-PAHs) were determined in 45 surface sediment and 7 basal sediment box core samples retrieved from the Estuary and Gulf of St. Lawrence in eastern Canada. The concentration sums of 16 priority PAHs (Σ16PAHs) in the surface sediments (representing modern times or at least younger than the last decade) ranged from 71 to 5672 ng g-1. Σ16PAHs in the basal sediments ranged from 93 to 172 ng g-1 among the pre-industrial samples (pre-1900 common era or CE) and from 1216 to 1621 ng g-1 among the early post-industrial samples (~1930s and ~1940s CE). The highest Σ16PAH values occurred in samples retrieved from the Baie-Comeau-Matane area, an area affected by intense industrial anthropogenic activities. Source-diagnostic PAH ratios suggest a predominance of pyrogenic sources via atmospheric deposition, with a minor contribution of petrogenic seabed pockmark sources. The PAH concentrations in the sediments from the study areas reveal low ecological risks to benthic or other organisms living near the water-sediment interface.

Spatial and temporal distributions of polycyclic aromatic hydrocarbons in sediments from the Canadian Arctic Archipelago.

The concentrations of 23 polycyclic aromatic hydrocarbons (PAHs; 16 parent and 7 alkylated PAHs) were determined in 113 surface marine sediment samples, 13 on-land sediment samples and 8 subsampled push cores retrieved from the Canadian Arctic Archipelago (CAA). PAHs were extracted via accelerated solvent extraction and quantified via gas chromatography-mass spectrometry. The sums of the concentrations of 16 priority PAHs in the surface sediments ranged from 7.8 to 247.7 ng g-1 (dry weight basis, dw). The PAH inputs to the sediments have remained constant during the last century. Source-diagnostic ratios and statistical analysis suggest that the PAHs in the CAA mainly originate from natural petrogenic sources, with some pyrogenic sources. Temporal trends did not indicate major source shifts and largely indicated petrogenic inputs. Overall, the sediments retrieved from the CAA have low PAH concentrations, which indicates a low ecological risk for benthic or other organisms living near the water-sediment interface.

Under ice spills of conventional crude oil and diluted bitumen: Physiological resilience of the blue mussel and transgenerational effects.

Spillages at sea of diluted bitumen (dilbit) from oil sands have received little attention until now. To our best knowledge, there are no reports on the impact of a severe exposure to dilbit on the Blue mussel (Mytilus edulis). In this study, adult Blue mussels were exposed to one conventional crude oil (Heidrun) and two dilbits (Cold Lake Blend and Access Western Blend) for a period of 7 days in an ice-covered environment and then maintained for three months until the spawning season. The exposed mussels were monitored for aromatic hydrocarbon bioaccumulation, physiological energetic budget, cellular stress, byssus production and gametogenesis. In spring, spawning was induced to characterize breeding success. Bioaccumulation of polycyclic aromatic hydrocarbons (PAHs) was detected after three days of exposure, with higher concentrations of PAHs associated to the conventional oil (5.49 ± 0.12 µg·g-1 d.w.) compared to both dilbits (0.91 ± 0.02 µg·g-1; 0.51 ± 0.03 µg·g-1 d.w.). Despite a fast depuration rate and a good resilience of the exposed mussels, significant negative effects were observed at the cellular, physiological and fitness levels, especially in offspring. Our results suggest a higher toxicity of the diluted bitumen compared to the conventional crude despite the lower bioaccumulation of total PAHs. Dilbit treatments caused evident negative transgenerational effects on unexposed F1 generation.

Selected dehydrogenases in Yarrowia lipolytica JMY 861: their role in the synthesis of flavor compounds.

The presence of selected dehydrogenases, including alcohol dehydrogenase (ADH-YL) and aldehyde dehydrogenase (ALDH-YL), in Yarrowia lipolytica JMY 861, and their potential role in flavor synthesis were investigated. The experimental findings showed that using reduced form of nicotinamide adenine dinucleotide (NADH) as cofactor, the ADH-YL activity in vitro was 6-fold higher than that with reduced form of nicotinamide adenine dinucleotide phosphate (NADPH); however, under the experimental conditions used in this study, an ALDH-YL activity was not detected. The in situ hexanal reduction reaction was found to be instantaneous; however, when the yeast cells suspension was diluted 150 times, the initial relative hexanal concentration was increased by 84.1%. The chromatographic analyses indicated the conversion, in situ, of linoleic acid hydroperoxides (HPODs) into volatile C6-compounds after 60 min of HPODs addition to the yeast cells suspension.

Presence and distribution of persistent toxic substances in sediments and marine organisms of Potter Cove, Antarctica.

Levels of butyltin compounds, polychlorinated biphenyls, and heavy metals were analyzed in marine sediments and organisms (Notothenia coriiceps, Laternula elliptica, and Nacella concinna), each of which has a different feeding strategy, in Potter Cove, Antarctica. PCBs were lower than detection limits in all samples. Only butyltin compounds were detected in a restricted area near the scientific station. Chromium, copper, magnesium, lead (Pb), and zinc had similar behavior in the cove, probably because they are regulated by similar process and conditions. However, Pb levels in some sites of the cove seem to be related to human activities in the area. Cadmium levels were relatively low, with the highest values found close to the shoreline, which is probably influenced by seasonal streams draining waters from Potter Peninsula. Results showed that despite the fact that Jubany Station has been operating for > 50 years, surface sediment and biota from Potter Cove do not exhibit levels of pollutants representing environmental concern.

Sorption characteristics of polycyclic aromatic hydrocarbons in aluminum smelter residues.

High temperature carbon oxidation in primary aluminum smelters results in the release of polycyclic aromatic hydrocarbons (PAH) into the environment. The main source of PAH are the anodes, which are composed of petroleum coke (black carbon, BC) and coal tar pitch. To elucidate the dominant carbonaceous phase controlling the environmental fate of PAH in aluminum smelter residues (coke BC and/or coal tar), the sorptive behavior of PAHs has been determined, using passive samplers and infinitesink desorption methods. Samples directly from the wet scrubber were studied as well as ones from an adjacent 20-year old storage lagoon and roof dust from the smelter. Carbon-normalized distribution coefficients of native PAHs were 2 orders of magnitude higher than expected based on amorphous organic carbon (AOC)/water partitioning, which is in the same order of magnitude as reported literature values for soots and charcoals. Sorption isotherms of laboratory-spiked deuterated phenanthrene showed strong (-100 times stronger than AOC) but nonetheless linear sorption in both fresh and aged aluminum smelter residues. The absence of nonlinear behavior typical for adsorption to BC indicates that PAH sorption in aluminum smelter residues is dominated by absorption into the semi-solid coal tar pitch matrix. Desorption experiments using Tenax showed that fresh smelter residues had a relatively large rapidly desorbing fraction of PAH (35-50%), whereas this fraction was strongly reduced (11-16%) in the lagoon and roof dust material. Weathering of the coal tar residue and/or redistribution of PAH between coal tar and BC phases could explain the reduced availability in aged samples.

Lipase-catalyzed transesterification of dihydrocaffeic acid with flaxseed oil for the synthesis of phenolic lipids.

Lipase-catalyzed transesterification reaction of dihydrocaffeic acid (DHCA) with flaxseed oil in organic solvent media was investigated. Using equal molar concentration of DHCA and flaxseed oil, only phenolic monoacylglycerols were obtained with a transesterification yield (TY) of 18.9%. A 1:4 DHCA to flaxseed oil ratio resulted in the production of both phenolic mono and diacylglycerols, with TY of 39.6 and 27.8%, respectively. On the other hand, when 1:8 ratio of DHCA to flaxseed oil was used, the TY of phenolic diacylglycerols (46.0%) was higher than that of the phenolic monoacylglycerols (33.3%). The TY of phenolic diacylglycerols increased from 25.1 to 55.8%, when the ratio of the hexane/2-butanone reaction medium was changed from 65:35 to 85:25 (v/v); however, the TY of phenolic monoacylglycerols decreased slightly from 34.0 to 31.8%. The relative proportion of the C(18:3)n-3 was higher in the phenolic mono and diacylglycerols, 64.9 and 59.5%, respectively, as compared to the original flaxseed oil, 53.1%. The radical scavenging ability of phenolic lipids was significant; however, it was about half than that of alpha-tocopherol.

Highly persistent butyltins in northern marine sediments: a long-term threat for the Saguenay Fjord (Canada).

An exhaustive study of the distribution of butyltin species was conducted in the sediment of the Saguenay Fjord (Canada), a semi-enclosed marine system with sediment permanently submitted to sub-Arctic cold conditions. Concentrations of total butyltins (tributyltin [TBT], dibutyltin, and monobutyltin) ranged from 6 to 288 ng Sn/g dry weight and were typical of those reported for contaminated coastal areas despite limited seasonal traffic of commercial vessels in the fjord. The distribution profiles of butyltin species in four sediment cores clearly indicated the high persistence of TBT that was dominating other species. The particular oceanographic conditions of the Saguenay Fjord (low seawater temperature, anoxic sediments, and low exchange rate of deep waters) combined with a high sediment/pore-water partition coefficient (Kdobs = 1.0 x 10(4) to 1.2 x 10(4) L/kg) and a low sediment/ water diffusive flux of TBT (J1 = 13 x 10(-8) mol/m2/year) are responsible for the burial and preservation of TBT in this marine ecosystem. The half-life of TBT in deep sediment was estimated to be approximately 87+/-17 years (+/-SEM), which implies a much slower degradation rate than any previously reported. Finally, a flood event that occurred five years before the sampling enabled us to calculate a very slow diffusive flux from the preflood to the postflood layer (J2 = 2 x 10(-8) mol/m2/year), indicating an almost permanent sequestration of TBT in the buried layers.

Degradation of petroleum hydrocarbons in two sub-antarctic soils: influence of an oleophilic fertilizer.

In order to determine the long-term effects of fertilizer on the degradation rate and the toxicity of hydrocarbons in sub-Antarctic soils contaminated by petroleum hydrocarbons, a field study was initiated in December 2000 on two different soils of the Kerguelen Islands (69 degrees 42'E, 49 degrees 19'S). The number of hydrocarbon-degrading bacteria (HDB) increased greatly after crude-oil and diesel-fuel contamination, and the fertilizer addition had a favorable effect on HDB growth and activity. Hydrocarbon-degrading bacteria counts remained high until the end of the experiment although the total hydrocarbon content in all contaminated soils was reduced to 80 to 90% of their initial value after 330 d. Degradation of n-alkanes was enhanced significantly in the presence of the fertilizer, while the degradation of polycyclic aromatic hydrocarbons (PAHs) was only barely enhanced. Toxicity results showed a noticeable reduction with time, although toxicity remained present and important in both soils at the end of the experiment. In addition, fertilized plots showed a toxic signal greater than unfertilized ones. Overall results clearly show that fertilizer addition improves the rate of degradation of both oil contaminants. However, remaining toxic residues may constitute a drawback of the fertilizer-assisted biodegradation process at low temperatures.