Water-use efficiency is an important functional trait that can be defined at very different temporal and spatial scales in trees as well as in crops. Transpiration efficiency (TE) is usually defined at tree or even stand level as the ratio between transpired water and accumulated biomass. Intrinsic water-use efficiency (Wi) is defined at instant leaf scale as the ratio net CO2 assimilation rate vs. stomatal conductance (A/gs). Wi is usually estimated by isotopic discrimination against 13CO2 during photosynthesis (Delta). Delta can be measured at the instantaneous time-scale on-line with new spectroscopic techniques, but is usually recorded from the isotopic composition of different metabolic pools (bulk leaf matter, soluble sugars, cellulose in leaves and wood). Delta is a plastic trait and is therefore largely used as an index for short term (interannual) changes in water availability and for climate constraints. Delta is also under tight genetic control in trees like in many other species and shows a large diversity. This was shown for populations from different origins, within populations on ecological clines, and among clones. Furthermore, quantitative genetics approaches identified a few highly significant QTLs for Delta in full-sib offsprings of oaks, maritime pine, chestnut and poplars, and thus identified a small number of genomic regions that are active in the control of Delta. The range of genotypic values identified in these approaches encompasses up to 3-4 ‰, which would translate into 30-50% difference in intrinsic water-use efficiency. Due to technical difficulties, much less evidence is available about the genetic control of Wi and of TE. Moreover, the parameters of the model relating Delta to Wi may also display some degree of genotypic variability, and the suitability of Delta as an index for Wi has been questioned. In this presentation, some evidence will be produced in support for the tight correlation between Delta and Wi in support of the use of Delta as a screening tool for Wi and even TE. Based on the accumulated data demonstrating the large diversity of Wi as well as the tight genetic control over this trait, a few research perspectives will be identified and discussed

The common mussel Mytilus galloprovincialis was selected as unique biomonitor species to implement a regional monitoring programme, the CIESM Mediterranean Mussel Watch (MMW), in the Mediterranean and Black Seas. As of today, and upon standardization of the methodological approach, the MMW Network has been able to quantify Cs-137 levels in mussels from 60 coastal stations and to produce the first distribution map of this artificial radionuclide at the scale of the entire Mediterranean and Black Seas. While: measured Cs-137 levels were found to be very low (usually <1 Bq kg(-1) wet wt) Cs-137 activity concentrations in the Black Sea and North Aegean Sea were up to two orders of magnitude higher than those in the western Mediterranean Basin. Such effects, far from representing a threat to human populations or the environment, reflect a persistent signature of the Chernobyl fallout in this area. (C) 2007 Elsevier Ltd. All rights reserved.

To investigate the consequences of acidification and metal accumulation on the biology of aquatic bryophytes, the acid-tolerant liverwort Scapania undulata (L.) Dum. and the acid-sensitive moss Rhynchostegium riparioides (Hedw.) Cardot were transplanted from one stream to two other streams of differing acidity (pH 5.20 and 6.38). The bryophytes were collected in a circumneutral (pH 6.57) stream in the Vosges Mountains. Metal accumulation was semiquantitatively measured in shoots by energy dispersive TEM X-ray spectroscopy (EDXS). After 1 month, the two species remained green without alteration signs. Although no marked ultrastructural damage was observed in either species, some cells seemed to be necrotic, with flattened chloroplasts, in R. riparioides. Lipid droplet accumulation was observed in some leaf cells of S.undulata when transplanted to the most acidic stream. Metal was mostly localised in the cell wall, and was only sometimes detected in small vacuoles. Under acidic conditions, R. riparioides showed the highest relative amount of Al and the lowest amount of Fe, whereas the acid-tolerant bryophyte species S. undulata contained more Fe and less Al. The capability to limit the uptake of metals into the cytoplasm varies according to the bryophyte species. This could be an explanation of the tolerance of S. undulata to acidification. | International audience

A simple analytical method for the quantitative analysis of fluoroquinolone group antibiotics, enrofloxacin (ENR) and ciprofloxacin (CIP) in soil was developed based on the mechanical extraction with vortex and ultrasonication and solid phase extraction followed by high pressure liquid chromatography-fluorescence detection (HPLC-FLD). Type of extraction solvents and number of extraction cycles were optimized during the method development. The most efficient extraction solvent was found as phosphate buffer at pH 3 in combination with 50% of organic modifier acetonitrile with the extraction cycle of four. Overall method was applied on three different types of soils, namely, sandy, loamy sand and sandy loam and recovery rates ranged between 71-100% for ENR and 61-89% for CIP depending on the portion of organic and clay content in soils. The analytical method was also used for the estimation of fluoroquinolone concentrations in manure amended agricultural soils sampled from the different parts of Turkey and enrofloxacin was detected in the concentration range of 0.013-0.204 mg/kg. In addition, sorption of fluoroquinolone antibiotics on all types of soils was investigated and the highest distribution coefficients (Kd and Kf) of fluoroquinolone compounds were obtained for loamy sand (Kd = 1.29 l/g and Kf = 0.66 for CIP; Kd = 0.97 l/g and Kf = 0.56 for ENR) with the highest organic carbon.

Nonylphenol is the primary breakdown product of nonylphenol ethoxylates, a certain class of nonionic surfactants. Nonylphenol has been found to be toxic to aquatic organisms and has been suspected of being harmful to humans due to its xenoestrogenic properties. Although there are known releases of nonylphenol to the environment, there is a lack of data describing the extent of biodegradation. This study thus focuses on much needed information on the biodegradation kinetics of nonylphenol. Oxygen uptake, cell growth and nonylphenol removal data were collected using batch reactors in an electrolytic respirometer. Nonylphenol removal, cell growth and substrate removal rates were modeled by the Monod, Haldane, Aiba, Webb, and Yano equations. The differential equations were solved by numerical integration to simulate cell growth, substrate removal, and oxygen uptake as a function of time. All models provided similar results with the Haldane model providing the best fit. The values of the kinetic parameters and the activation energy for nonylphenol were determined. These values can be used for predicting fate and transport of nonylphenol in the environment. The validity of applying each model to the biodegradation of nonylphenol was analyzed by computing the R ² values of each equation.

This paper summarizes substance flow analyses for four organic substances in the City of Stockholm, Sweden: diethylhexyl phthalate (DEHP), alkylphenolethoxylates (APEO), polybrominated diphenylethers (PBDE) and chlorinated paraffins (CP). The results indicate that the stocks of APEO, PBDE and CP all are approximately 200-250 tonnes, whereas the DEHP stock is two orders of magnitude larger. Emissions can be linked to imported consumer goods such as electronics (PBDE) and textiles (APEO), and to construction materials (DEHP, CP). For several of the substances considerable amounts remain in the technosphere for a long time, even after use of the substance in new products has been eliminated. For example, the use of DEHP as plasticizer for PVC plastics in cables and floorings has more or less been phased-out, but still these applications make up a stock of some 20,000 tonnes (85% of the total DEHP stock in Stockholm) and emit 28 tonnes of DEHP annually (93% of overall emissions). Likewise, the use of chlorinated paraffins in sealants has been radically reduced, but there are 170 tonnes of CP in sealants in Stockholm making up 75% of the stock, and causing half of the emissions to water and air. These emissions are likely to continue for decades, and the stocks therefore have to be considered when analysing and managing the impact of urban substance flows on the environment.

While hydrophilic compounds are degraded easily in Trickling bed air biofilters (TBABs), hydrophobic compounds are retarded until biological cultures produce a sufficient RNA or enzyme/protein to utilize this compound. Hydrophobic compounds are not readily bio-available which makes them reluctant to biodegradation as mass transfer between the gas and liquid phases is a rate limiting step. To enhance the destruction of hydrophobic compounds in TBABs, the utilization of surfactant was introduced to increase the solubility which helps overcoming the rate limiting step. The surfactant was used as well to limit the growth of excess biomass ensuring smooth flow through the biofilter bed and preventing short circuits. Two different non-ionic non-toxic surfactants were used in this study: Triton X-100 and Tomadol® 25-7. Two lab-scale controlled TBABs were operated for investigating the performance difference for n-Hexane as an example of hydrophobic volatile organic compound (VOC) with and without the addition of surfactant. Operating conditions in both TBABs were as follows: nutrient feed rate (2L/day), air flowrate (1.4L/min), bed depth (60cm), empty bed retention time (120s), bed material (diatomaceous earth pellets) and room-temperature. The inlet concentration was changed from 50 to 100ppmv. Acclimation period, removal profile along biofilter depth, nitrogen consumption, and CO₂ production were compared under continuous loading operation condition. The optimum concentration of surfactant in the nutrient feed was determined by a batch experiment. The effect of different surfactant concentrations on VOC water solubility with time was studied by considering different VOC concentration sets within the TBAB loading rate range.

In this study, we evaluated the relative contribution of atmospheric particulate mercury (Hg(p)) and divalent reactive gaseous mercury (RGM) to mercury dry deposition in Japan. The dry deposition fluxes (on a water surface sampler) and atmospheric PM concentrations of Hg, Cd, Cu, Mn, Ni, Pb and V, which were measured concurrently from April 2004 to March 2006 at 10 sites across the nation, were used in this evaluation. We considered that Hg(p) and RGM, but not Hg⁰, are deposited on the water surface, and that our method of sampling Hg(p) without the use of KCl-coated annular denuders enables the exclusion of a significant amount of RGM artifact. The monthly average dry deposition velocities (= deposition flux/atmospheric PM concentration) of Cd and Pb were found to be similar to each other (Cd/Pb deposition velocities = 1.06 ± 0.58). It was assumed that the deposition velocity of Hg(p) is identical to the mean deposition velocity of Cd and Pb, because the particle size distribution of Hg(p) is likely similar to those of both elements. Using this deposition velocity, the monthly dry deposition flux of Hg(p) was calculated. The average contribution (±1σ) of Hg(p) to the annual deposition flux at ten sites was 26 ± 15%. The mercury dry deposition flux increased generally from spring to early summer, which was attributed mostly to the deposition of RGM. This seasonal change correlated to that in photochemical oxidant (primarily O₃) concentration in air at most sites. These suggest that mercury dry deposition in Japan is predominantly deposition of RGM, which was formed via oxidation of Hg⁰ by O₃ in the atmosphere.

The presence of alpha emitting radionuclides in the environment assumes importance since they are found to be carcinogenic. This paper reports the results of an exhaustive and systematic measurement of alpha radioactivity using solid state nuclear track detector (SSNTD) in drinking water in different parts of India covering the entire Ganges Basin - West Bengal, Bihar and Uttar Pradesh where arsenic contamination is severe. The alpha activity in the samples was found in the range of 8 to 800 Bq/l in West Bengal, 90 to 1,000 Bq/l in Uttar Pradesh and 60 to 1,000 Bq/l in Bihar - much higher alpha activity value than MCL value given by US EPA. The concentration of alpha activity has a positive correlation with that of arsenic.