Temporal variation in protein, carbohydrate, and lipid concentrations in Paramuricea clavata (Anthozoa, Octocorallia): evidence for summer–autumn feeding constraints

Temporal variations in protein, carbohydrate, and lipid levels were studied in a passive suspension feeder, the gorgonian Paramuricea clavata. The samples were collected every month for mature and immature colonies over a three-year period (1997–2000). The relationship between biochemical composition and reproductive output was examined on the basis of the 1998 and 1999 data. In female and male P. clavata colonies, the tissue displayed differences in lipid concentrations only in winter–spring, due to the high lipid levels attained by female colonies in this period. Immature colonies showed significant differences in lipid concentration only with respect to mature females in spring. There were clear seasonal trends in the lipid and carbohydrate levels in P. clavata, with maximum values in winter–spring [male lipid 212±75 SD μg mg⁻¹ of organic matter (OM) and female lipid 274±103 SD μg mg⁻¹ of OM; male and female carbohydrate 68±14 SD μg mg⁻¹ of OM], coinciding with maximum food concentration/quality, and minimum values in summer–autumn (male and female lipid 155±57 SD μg mg⁻¹ of OM; male and female carbohydrate 56±14 SD μg mg⁻¹ of OM), coinciding with low food concentration/quality. The relationship between reproductive output and tissue concentrations of lipids, carbohydrates, and proteins was not straightforward, although there was an evident overlap of the lipid accumulation and the gonadal development. The results of this study show that protein, carbohydrate, and lipid levels may provide a record of episodes in the ecological cycle bearing on the trophic aspects of the target species. The results indicate that information on seasonal biochemical levels may explain benthopelagic coupling processes, provided factors such as natural diet, feeding rates, reproduction, and growth are well understood.     

Agricultural practices in grasslands detected by spatial remote sensing

The major decrease in grassland surfaces associated with changes in their management that has been observed in many regions of the earth during the last half century has major impacts on environmental and socio-economic systems. This study focuses on the identification of grassland management practices in an intensive agricultural watershed located in Brittany, France, by analyzing the intra-annual dynamics of the surface condition of vegetation using remotely sensed and field data. We studied the relationship between one vegetation index (NDVI) and two biophysical variables (LAI and fCOVER) derived from a series of three SPOT images on one hand and measurements collected during field campaigns achieved on 120 grasslands on the other. The results show that the LAI appears as the best predictor for monitoring grassland mowing and grazing. Indeed, because of its ability to characterize vegetation status, LAI estimated from remote sensing data is a relevant variable to identify these practices. LAI values derived from the SPOT images were then classified based on the K-Nearest Neighbor (KNN) supervised algorithm. The results points out that the distribution of grassland management practices such as grazing and mowing can be mapped very accurately (Kappa index?=?0.82) at a field scale over large agricultural areas using a series of satellite images.     

Fluorescence Verses Radioactivity Labeling for Lab-Scale Investigation of the Fate of Water-Soluble Polymers in Wastewater Treatment Plants

Water-soluble synthetic polymers are extensively used in cosmetics, detergents and paints. Many end up in wastewater and, later on, in wastewater-treatment plants. In order to gain an insight into their fate in such plants, fluorescence and radioactivity labelings were compared using a lab-scale reactor designed to mimic industrial conditions. Two fermentation media were considered, namely a mixture of E402 and E204 micro-organisms and an activated sludge collected from a water-treatment plant located in the south of France. A sample of low molar mass commercial poly(acrylic acid) (PAA) was labeled by radioactivity with tritium and by coupling the 6-aminofluorescein fluorescent dye. Labeled PAA-containing sludges were allowed to ferment. To monitor the fate of the polymers, aliquots of the fermented mixtures were withdrawn at selected times and centrifuged. Liquid and solid phases were analyzed by scintigraphy or UV spectrometry, depending of the labeling techniques. Both techniques led to similar distributions, c.a. 75% in the supernatant and 25% in the solid phase. Distributions remained constant during the biological tests. There was no degradation of the commercial PAA after aqueous size exclusion chromatography (SEC), in agreement with literature. These features showed that fluorescence-labeling can be used instead of the complex and expensive radiolabeling. The validated fluorescence-based method was then applied to a linear poly(acrylic acid) synthesized by ATRP and labeled with 6-aminofluorescein. There was no significant difference between the commercial and the linear poly(acrylic acid)s. In contrast, a linear PAA with 5% of tert-butyl ester repeating units was predominantly found in the solid phase although adsorption or absorption by micro-organisms could not be demonstrated. The method based on fluorescence labeling should be applicable to other water soluble polymers provided that the dye remains attached to the polymer as it was the case for the studied poly(acrylic acid)s.     

Capillary electrophoresis to analyze water-soluble oligo(hydroxyacids) issued from degraded or biodegraded aliphatic polyesters

In an attempt to increase the range of analytical techniques able to monitor ultimate degradation stages of degradable, biodegradable, and bioresorbable polymers, capillary zone electrophoresis (CZE) was used to analyze tentatively oligomers formed during thermal condensation of lactic, glycolic, anddl-3-hydroxybutyric acids. The influence of the buffer and of capillary coating are discussed in terms of electroosmotic flow. Typical analyses were first performed using a 0.1M borate buffer (pH 8.9) with anodic injection. In the case of lactic acid, seven peaks were well separated, while only three peaks were observed for glycolic acid. A more complex situation was found fordl-3-hydroxybutyric acid oligomers. The first five peaks were split. The major component of each doublet was attributed to hydroxy-terminated oligomers, whereas the satellite peaks were assigned to oligomers bearing a C=C double bond at the noncarboxylic terminus. CZE of pH-sensitive lactic acid oligomers was also performed in 0.05M phosphate buffer (pH 6.8) with cathodic injection after physical coating of the fused-silica capillary with DEAE-Dextran. The buffer-soluble fraction present in lactic acid oligomers was extracted from a dichloromethane solution. Extracts issued from different batches of lactic acid condensates gave a constant water-solubility pattern whose cutoff was at the level of the decamer. CZE was also used to monitor thein vitro aging of aqueous solutions of these water-soluble oligomers. The lactyllactic acid dimer appeared more stable than higher oligomers, thus showing that ultimate stages of the degradation did not proceed at random. These physicochemical characteristics were used to complement the degradation pathway based on diffusion of oligomers duringin vitro aging of large size lactic acid plates made by compression molding. CZE data showed that lactic acid was the only component which was released in the aqueous medium during degradation.Presented by C.B. at the 4th International Workshop on Biodegradable Plastics and Polymers, October 11–14, 1995, Durham, NH, USA.     

Metsulfuron‐methyl soil persistence and mobility in winter wheat and following green manure crops

A procedure has been developed for the analysis of metsulfuron‐methyl in the soil of field crops. The soil extracts are cleaned by repeated TLC, and metsulfuron‐methyl is simultaneously separated from its soil metabolites. Metsulfuron‐methyl is transformed by diazomethane into its N,N ‘‐dimethyl derivative which in the GC (electron capture detection) and GC‐MS apparatus is transformed into a benzisothiazole compound which is measured with great sensitivity. The sensitivity limit is 0.3 μg metsulfuron‐methyl kg^‐1 dry soil. The results of the chemical analyses are confirmed by bioassays using sugar beet as test plant. Metsulfuron‐methyl was measured in the soil of two winter wheat crops after post‐emergence application in the spring of 6 g metsulfuron‐methyl ha^‐1. In the 0–8 cm surface soil layer, the metsulfuron‐methyl soil half‐life was 78 days in 1997, and 67 days in 1998. During crop, metsulfuron‐methyl remained in the 0–8 cm surface soil layer. There, it was at a maximum concentration and herbicide efficiency in a 2 cm‐thick soil layer. This maximum concentration soil layer progressively moved down during crop, attaining the 4–6 cm surface soil layer at crop end. After the winter wheat harvest at the end of July, and the rotary‐tilling of the 0–10 cm surface soil layer before sowing of the green manures, 27% of the metsulfuron‐methyl initial dose still remained in the 0–10 cm surface soil layer. This residue progressively disappeared, and was no more detected at the middle of November. It had no, or only very low inhibiting effect on the growth of the green manures. Thus there is no concern about the possible phytotoxicity of persistent metsulfuron‐methyl soil residues towards the following crops, when metsulfuron‐methyl is applied at the rate of 6 g a.i.ha^‐1.     

Mobility and adsorption of the triketone herbicide mesotrione in the soil of corn crops

The triketone herbicide mesotrione has been applied pre‐emergence at the dose of 150 g a.i. ha^?1 on corn fields grown within the same period of time at different sites on clay, loam, sandy loam or sandy soils. During the crops and one month after the corn harvest, the mobility of mesotrione has been measured in the 0–20 cm surface soil layer, soil samples being taken in the 0–2,2–4,4–6,6–8, 8–10, 10–15 and 15–20 cm surface soil layers. During the first month after the treatment, mesotrione remained in the 0–2 cm surface soil layer. Thereafter, mesotrione was at a higher concentration in a 2 cm‐thick soil layer which progressively moved down in the clay, loam and sandy loam soils. In the sand soil, mesotrione moved down as a uniform diffusion, its concentration being similar in all the 2 cm‐thick layers of the 0–10 cm soil surface layer. Low mesotrione residues (6–10 ug kg^?1 dry soil) attained the 10–15 cm layer faster in the clay and sand soils than in the loam and sandy loam soils. Mesotrione was not detected in the 15–20 cm soil layer of the loam and sandy loam soils, but well in the sand and clay soils. In the soils of the corn crops mesotrione thus mainly remained in the 0–10 cm surface soil layer. This low mobility and depth of penetration conjugated to the rate of mesotrione soil degradation explain why there was no movement of mesotrione toward the deeper soil layers. The adsorption of mesotrione was greatest on the soils recently treated with organic fertilizers, and having a loam or sandy loam texture. The adsorption coefficients explained the lower mobility and the greatest persistence of mesotrione in these soils.     

Mechanical Properties and Lipase-Catalyzed Biodegradation of α-Methyl, ε-Caprolactone/ ε-Caprolactone Copolymers Obtained by Chemical Modification of Poly(ε-caprolactone)

Novel (-caprolactone)-based copolymers of different compositions were synthesized by allowing methyl iodide to react with the polycarbanion that resulted from the action of lithium diisopropylamide on poly(-caprolactone) in THF at –70°C under argon atmosphere. The copolymers were characterized by various techniques, namely ¹H nuclear magnetic resonance, size exclusion chromatography, differential scanning calorimetry, x-ray diffraction and viscoelasticimetry. They were submitted to hydrolytic and lipase-catalyzed enzymatic degradation in comparison with genuine PCL. The Young modulus depended on the degree of methylation. In contrast, loss angle and glass transition temperature did not depend on this parameter. It is shown that the lipase-catalyzed degradation of methylated PCL is much slower than in the case of genuine PCL.