Spatial distribution of lindane in topsoil of Northern France

Lindane is a persistent organochlorine insecticide and the use of this insecticide in agriculture was banned in France in 1998. In this study we investigated the concentrations of lindane in topsoil in Northern France and used robust geostatistics to map the geographical distribution of lindane. The study was based on a 16 km × 16 km grid covering an area of ca 25 000 km². Lindane was found in all soils, even those from non-agricultural-application areas. Very low ratios of α-/γ-HCH and δ-/γ-HCH suggested that a long time had passed since technical HCH was used in the studied area, or that emission sources of lindane were still present. A strong gradient in lindane concentration was observed, with the highest lindane concentrations in an area located in the northern region. Results suggested that some of the lindane observed in the high concentration area may have come from volatilization of old lindane applied to intensively cultivated areas, which was then transported by prevailing winds coming from the south-west and deposited in a densely inhabited depression.     

Comparison of seasonal variations of ozone exposure and fluxes in a Mediterranean Holm oak forest between the exceptionally dry 2003 and the following year

Ozone and energy fluxes have been measured using the eddy covariance technique, from June to December 2004 in Castelporziano near Rome (Italy), and compared to similar measurements made in the previous year. The studied ecosystem consisted in a typical Mediterranean Holm oak forest. Stomatal fluxes have been calculated using the resistance analogy and by inverting the Penmann-Monteith equation. Results showed that the average stomatal contribution accounts for 42.6% of the total fluxes. Non-stomatal deposition proved to be enhanced by increasing leaf wetness and air humidity during the autumnal months. From a comparison of the two years, it can be inferred that water supply is the most important limiting factor for ozone uptake and that prolonged droughts alter significantly the stomatal conductance, even 2 months after the soil water content is replenished. Ozone exposure, expressed as AOT40, behaves similarly to the cumulated stomatal flux in dry conditions whereas a different behaviour for the two indices appears in wet autumnal conditions. A difference also occurs between the two years.     

Importance of natural sedimentation in the fate of microcystins

Sedimentation processes of microcystins (MCs), cyanobacterial toxins, were studied in three reservoirs located in Central Spain in which the cyanobacterial community was dominated by the genus Microcystis. MCs were detected in the sediment traps deployed in all reservoirs. In Santillana reservoir, MCs were identified in sediment traps even though they could not be found in the pelagial samples. In the other reservoirs studied, sedimentation rates for MC-containing particles during the bloom period ranged from 0.43 to 2.53 mg m⁻² d⁻¹. Interestingly, this very high sedimentation of toxic biomass is not exclusively related to decaying blooms or autumnal sedimentation due to a drop in water temperature. Instead, it seems that MC-containing colonies may be settling constantly during the bloom period and we were able to estimate that during such a Microcystis dominated bloom, around 4.5% of pelagial MCs may be involved in sedimentation. Further, these settling colonies seem to maintain good cell integrity and MCs seem not to be excreted massively. A certain loss of toxin content along the vertical settling may be attributed to minor losses due to cell lysis or to variations in MC cell quota explained by reduced production or internal consumption. Our results for the first time establish specific settling rates for MC-containing particles in freshwaters and definitely identify sedimentation as a major destination for these toxins. These data may contribute to improve managing strategies concerning risks associated with MCs.     

Decadal changes in atmospheric CO2 concentration and δ13C over two seas and two oceans: Italy to New Zealand

Continuous measurements of the CO₂ concentration were repeatedly carried out from 1996 to 2007 between Italy and New Zealand by means of a Siemens Ultramat 5E analyzer assembled for shipboard use. Along the ship routes discrete air samples were collected from 1998 to 2005 using four-litre Pyrex flasks. The δ¹³C of the CO₂ from the flask air samples was measured according to well-established techniques. The decadal changes of these two variables can now be evaluated from these results. Large variations of the CO₂ concentration were normally recorded in the Mediterranean and the Red Sea. Completely different trends of the CO₂ concentration were observed in the Red Sea (30° N to about 13° N) between 2007 (a marked southward decrease) and 2005 and 2003 when a marked southward increase is apparent, at least between 23° and 13° N. A further difference among different expeditions is related to the decrease or increase of the CO₂ concentration in the Gulf of Aden. The backward trajectories of the air masses help to explain, at least partially, these differences. In the Indian Ocean and Southern Ocean a decrease of a few ppmv of the CO₂ concentration takes place from Cape Guardafui (Northern Somaliland) to southern New Zealand, particularly during 2005 and 2007. The yearly rate of increase of the CO₂ concentration between 1996 and 2007 for the Indian Ocean is of about 1.9 ppmv yr^?1, in excellent agreement with the NOAA/CMDL measurements carried out during the same period at Mahé Isld. (Indian Ocean) and Cape Grim (Tasmania). The δ¹³C results obtained from the CO₂ of flask samples collected in the Mediterranean show the effect of anthropogenic emissions, though this is considerably smaller than expected. This inconsistency may be related to the large terrestrial biospheric sink of CO₂ in the Northern Hemisphere. The results obtained from the Red Sea are quite variable through time and space, particularly in its southern section; their interpretation is not easy. The Indian Ocean and the Southern Ocean show rather homogeneous δ¹³C results even though a variable carbon isotope shift can be calculated from period/cruise to period/cruise. In the case of the Indian Ocean the mean δ¹³C value from the flask air samples collected in 2005 is ?8.29‰ and the calculated rate of the carbon isotope shift between 1998 and 2005 is ?0.034‰ yr^?1, considerably larger than that calculated at the closest NOAA station (Mahé Isld.) of ?0.026‰ yr^?1. This discrepancy may be, at least partially, caused by the small number of measurements carried out at sea. However, the atmosphere over the Indian Ocean is less affected by anthropogenic emissions than in other areas.     

A Management Tool for Assessing Aquaculture Environmental Impacts in Chilean Patagonian Fjords: Integrating Hydrodynamic and Pellets Dispersion Models

This article introduces a management tool for salmon farming, with a scope in the local sustainability of salmon aquaculture of the Aysen Fjord, Chilean Patagonia. Based on Integrated Coastal Zone Management (ICZM) principles, the tool combines a large 3-level nested hydrodynamic model, a particle tracking module and a GIS application into an assessment tool for particulate waste dispersal of salmon farming activities. The model offers an open source alternative to particulate waste modeling and evaluation, contributing with valuable information for local decision makers in the process of locating new facilities and monitoring stations.     

Impact of underestimating the effects of cold temperature on motor vehicle start emissions of air toxics in the United States

Analyses of U.S. Environmental Protection Agency (EPA) certification data, California Air Resources Board surveillance testing data, and EPA research testing data indicated that EPA's MOBILE6.2 emission factor model substantially underestimates emissions of gaseous air toxics occurring during vehicle starts at cold temperatures for light-duty vehicles and trucks meeting EPA Tier 1 and later standards. An unofficial version of the MOBILE6.2 model was created to account for these underestimates. When this unofficial version of the model was used to project emissions into the future, emissions increased by almost 100% by calendar year 2030, and estimated modeled ambient air toxics concentrations increased by 6-84%, depending on the pollutant. To address these elevated emissions, EPA recently finalized standards requiring reductions of emissions when engines start at cold temperatures.     

Spatial and temporal trends of polycyclic aromatic hydrocarbons in wild mussels from the Cantabrian coast (N Spain) after the Prestige oil spill

Polycyclic aromatic hydrocarbon (PAH) levels were determined in tissues of wild mussels (Mytilus galloprovincialis) collected at 17 stations along the Cantabrian coast (N Spain), from Navia (Asturias) to Fuenterrabía (Basque Country), in order to assess the extent of the environmental impact caused by the Prestige oil spill (November 13, 2002). Six sampling campaigns were carried out in April, June and November in 2003 and 2004. The comparison of PAH data with those obtained earlier in 2000 showed a widespread pyrolytic and petrogenic contamination and allowed an estimation, for the first time, of the background pollution in the region and identification of the chronic hotspots. The spatial distribution found in the first samples after the oil spill revealed the eastern area as the most affected due to the continuous arrival of fuel slicks since early summer 2003. Several stations in this area showed increased total PAH concentrations of up to 15 times the pre-spill levels, which did not recover until April 2004, more than one year after the accident. Molecular parameters within the aliphatic and aromatic fractions were determined to assess the presence of Prestige oil in these samples.     

Tracing the fate of PCBs in forest ecosystems

Forests were shown to play an important role in influencing atmospheric concentrations and transport of persistent organic pollutants (POPs) in the environment. World forests cover more than 4 billion hectares and contain up to 80% of the above ground organic carbon. Given the lipophilic nature of POPs, this suggests that forests can influence the environmental fate of POPs at a global scale. POP accumulation in forest canopies still presents points of concern given the complexity of these ecosystems. In particular, the role of ecological parameters such as LAI (leaf area index) and SLA (specific leaf area) and their dynamics during the growing season was not sufficiently investigated yet. This paper reviews, compares and interprets a unique case study in which air and leaf concentrations and deposition fluxes for selected polychlorinated biphenyls (PCBs) were measured in three different forest types exposed to the same air masses. In order to trace the air-leaf-soil path of these compounds, a dynamic model of POP accumulation into forest canopy was applied. The dynamics of the canopy biomass strongly affected the trend of leaf concentration with time. Growth dilution effect can prevent the more chlorinated compounds from reaching the partitioning equilibrium before litter fall, while the more volatile compounds can approach equilibrium in the range of few weeks. An amount of up to 60 ng of PCBs per square metre of ground surface was predicted to be stored in each of the selected forests at fully developed canopy. Dry gaseous deposition fluxes to forest canopy were estimated to reach a maximum value of about 0.5-1.5 ng m(-2) d(-1) during the spring period.     

Evaluation of GC-ion trap-MS/MS methodology for monitoring PCDD/Fs in infant formulas

The application of high resolution gas chromatography in combination with low resolution mass spectrometry with electron ionization and MS/MS detection (HRGC-MS/MS) is tested for its use in the analysis of PCDD/Fs in infant formulas. Development of the analytical method was based upon EPA directrices and international recommendations. Calibration linearity was tested and average relative response for any native and labelled compound over the five-point calibration range below 14% was found. The precision and accuracy of the proposed analytical procedure are also presented. Results obtained are in agreement with EPA criteria. The method is applied to the analysis of a number of initial and follow-on milk based infant formulas. In general, HRGC-MS/MS constitutes an interesting method for the analysis of dioxins in such matrices.     

Improving ecological risk assessment by including bioavailability into species sensitivity distributions: an example for plants exposed to nickel in soil

The variability of species sensitivity distribution (SSD) due to contaminant bioavailability in soil was explored by using nickel as metal of concern. SSDs of toxicity test results of Avena sativa L. originating from different soils and expressed as total content and available (0.01 M CaCl2) extractable concentration were compared to SSDs for terrestrial plants derived from literature toxicity data. Also the 'free' nickel (Ni2+) concentration was calculated and compared. The results demonstrated that SSDs based on total nickel content highly depend on the experimental conditions set up for toxicity testing (i.e. selected soil and pH value) and thus on metal bioavailability in soil, resulting in an unacceptable uncertainty for ecological risk estimation. The use in SSDs of plant toxicity data expressed as 0.01 M CaCl2 extractable metal strongly reduced the uncertainty in the SSD curve and thus can improve the ERA procedure remarkably by taking bioavailability into account.