Impact of storm Xynthia in 2010 on coastal agricultural areas: the Saint Laurent de la Prée research farm’s experience

Storm Xynthia crossed France’s western coast between 28th February and 1st March 2010. It hit the Vendée and Charente-Maritime departments hardest, as storm surge flooded up to 23,000 ha of coastal agricultural areas (i.e. polders), causing severe damage to farming operations. However, farm-level damage in the aftermath of seawater flooding is an issue that has rarely been explored in the literature. Here we investigated the effects of storm Xynthia on agriculture at the farm scale. We focused on the case study of Saint Laurent de la Prée research farm, a mixed crop–livestock system that was severely hit. All damages were described and economic losses were quantified for the years 2010 and 2011. The results show numerous consequences of the storm in terms of crop and fodder production losses, but also farm infrastructure repairs, crop restoration and animal health problems. Economic damage costs were high, reaching €71,720 in 2010 (€500/ha flooded) and €56,195 (€390/ha) in 2011 for the case study farm. The discussion highlights the farm-level impacts of seawater flooding and the crucial factors that can explain the damage caused to agriculture by storm events in coastal areas. The results are also discussed in the wider context of global warming which is expected to cause sea level rise and more frequent storm events in the future. The vulnerability of coastal agricultural areas to storms thus exposes broader issues of coastal flooding risk management and specifically the allied protection–remediation–adaptation measures. The conclusions underline the need for future research to address prospective scenarios and subsequent adaptive strategies.     

Release of substituents from phenolic compounds during oxidative coupling reactions

Phenolic compounds originating from plant residue decomposition or microbial metabolism form humic-like polymers during oxidative coupling reactions mediated by various phenoloxidases or metal oxides. Xenobiotic phenols participating in these reactions undergo either polymerization or binding to soil organic matter. Another effect of oxidative coupling is dehalogenation, decarboxylation or demethoxylation of the substrates. To investigate these phenomena, several naturally occurring and xenobiotic phenols were incubated with various phenoloxidases (peroxidase, laccase, tyrosinase) or with birnessite (delta-MnO(2)), and monitored for chloride release, CO(2) evolution, and methanol or methane production. The release of chloride ions during polymerization and binding ranged between 0.2% and 41.4%. Using the test compounds labeled with 14C in three different locations (carboxyl group, aromatic ring, or aliphatic chain), it was demonstrated that 14CO(2) evolution was mainly associated with the release of carboxyl groups (17.8-54.8% of the initial radioactivity). Little mineralization of 14C-labeled aromatic rings or aliphatic carbons occurred in catechol, ferulic or p-coumaric acids (0.1-0.7%). Demethoxylation ranged from 0.5% to 13.9% for 2,6-dimethoxyphenol and syringic acid, respectively. Methylphenols showed no demethylation. In conclusion, dehalogenation, decarboxylation and demethoxylation of phenolic substrates appear to be controlled by a common mechanism, in which various substituents are released if they are attached to carbon atoms involved in coupling. Electron-withdrawing substituents, such as -COOH and -Cl, are more susceptible to release than electron-donating ones, such as -OCH(3) and -CH(3). The release of organic substituents during polymerization and binding of phenols may add to CO(2) production in soil.     

Photochemical behaviour of carbendazim in aqueous solution

To elucidate the photochemical behaviour of carbendazim (or MBC) in superficial waters, photolysis studies have been carried out in aqueous solutions at several pH using a UV light source (high pressure mercury arc lamp) or a solar light simulator (xenon arc lamp). The kinetics of photodecomposition of carbendazim was determined using HPLC-DAD and the identification of photoproducts was carried out with HPLC-MS (ESI negative and positive mode). According to the experimental results carbendazim is a rather stable molecule in the dark or in environmental conditions. The pH influence of the environmental medium on the photodegradation rate has been confirmed. The photochemical process can be considerably accelerated in alkaline solutions using HPK-quartz irradiation (quantum efficiency at pH 9 phi = 3.1 x 10(-3) degraded molecule per absorbed photon) while the photodegradation is not as efficient under a simulated sun irradiation (quantum efficiency in the suntest phi = 10(-4) at pH 7). Three photoproducts have been tentatively identified in pure water: 2-aminobenzimidazole, benzimidazole isocyanate and monocarbomethoxy-guanidine (issued from the cleavage of the benzimidazole ring). The last one seems very stable and could be accumulated in the environment.     

Assessment of seasonal variability of biomarkers in three-spined stickleback (Gasterosteus aculeatus L.) from a low contaminated stream: implication for environmental biomonitoring

In this study, wild three-spined sticklebacks were sampled every six weeks, between April and October, in a low contaminated stream. For all fish, physiological indexes, such as condition factor, hepato-, gonado- and nephro-somatic index were calculated to determine fish condition and reproductive status. Moreover, a set of biomarkers including biotransformation enzymes, oxidative stress parameters, neurotoxicity and endocrine disruption markers was measured. The results allowed to determine biomarker variability due to fish gender or sampling season. For example, 7-ethoxyresorufin-O-deethylase activity, glutathione peroxidase as well as vitellogenin and spiggin exhibited strong gender differences. Conversely, lipoperoxidation and acethylcholinesterase activity were characterised by a lack of gender and seasonal variation, and can be considered as more robust parameters for a field application. The present work allowed to establish practical guideline for biomarker measurements in wild sticklebacks and to define a reference system which can be used to analyze variations in future monitoring studies.     

A laser flash photolysis study of the decay of SO4- and Cl2- radical anions in the presence of Cl- in aqueous solutions

The rate constant for the reaction of sulphate radical (SO4-) with Cl- has been determined using laser photolysis, at 248 nm, of peroxodisulphate anions to produce the radicals and time resolved optical absorption of the transient species (at 450 or 480 nm for SO4- and 350 nm for Cl2-) for the kinetic determinations. The experiments were performed, in the absence of added sulphate, as a function of temperature and ionic strength and yielded (at an ionic strength of 0.0157 M): kIV = (9.90+/-0.16) x 10(9) exp((-7.12+/-2.0) kJ mol(-1)/RT) M(-1) s(-1), where the errors reflect the 2sigma statistical error. This reaction produces Cl2-, the formation and decay of which were also monitored allowing a determination of the rate constant of its second-order self-recombination reaction which gave k = (6.50+/-1.40) x 10(8) M(-1) s(-1) at 293 K and zero ionic strength.     

Estimated effects of climate change on flood vulnerability of U.S. bridges

We assessed the potential impacts of increased river flooding from climate change on bridges in the continental United States. Daily precipitation statistics from four climate models and three greenhouse gas (GHG) emissions scenarios (A2, A1B, and B1) were used to capture a range of potential changes in climate. Using changes in maximum daily precipitation, we estimated changes to the peak flow rates for the 100-year return period for 2,097 watersheds. These estimates were then combined with information from the National Bridge Inventory database to estimate changes to bridge scour vulnerability. The results indicate that there may be significant potential risks to bridges in the United States from increased precipitation intensities. Approximately 129,000 bridges were found to be currently deficient. Tens of thousands to more than 100,000 bridges could be vulnerable to increased river flows. Results by region vary considerably. In general, more bridges in eastern areas are vulnerable than those in western areas. The highest GHG emissions scenarios result in the largest number of bridges being at risk. The costs of adapting vulnerable bridges to avoid increased damage associated with climate change vary from approximately $140 to $250 billion through the 21st century. If these costs were spread out evenly over the century, the annual costs would be several billion dollars. The costs of protecting the bridges against climate change risks could be reduced by approximately 30% if existing deficient bridges are improved with riprap.     

An update of the Worldwide Integrated Assessment (WIA) on systemic insecticides. Part 3: alternatives to systemic insecticides

Environmental Science and Pollution Research - Over-reliance on pesticides for pest control is inflicting serious damage to the environmental services that underpin agricultural productivity. The...