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.     

Monitoring the toxicity of phenolic chemicals to activated sludge using a novel optical scanning respirometer.

This paper reports the development of optical scanning respirometer for determining the toxicity of chemicals to activated sludge. The respirometer is used to measure the dissolved oxygen concentration by monitoring the luminescence intensity of ruthenium dye immobilized in a polymer film in contact with the wastewater sample. The intensity is related to the extent of oxygen quenching of luminescence. The toxicity of chemicals can be evaluated by measuring the inhibition on respiration rate of microorganism using the scanning respirometer. The IC50 values (concentration of a chemical that exhibits 50% respiration inhibition) of various phenolic chemicals in activated sludge were determined. The performance of this method is compared with other toxicity methods. The experimental results indicate that the reproducibility and sensitivity of this respirometer are reasonably good.     

CHEMICAL CONSTITUENTS IN STORM FLOW VS. DRY WEATHER DISCHARGES IN CALIFORNIA STORM WATER CONVEYANCES1

ABSTRACT: This research evaluated concentration data for selected water quality parameters in selected California urban separate storm sewer systems during storm event discharges and during dry weather conditions. We used existing monitoring data from multiple regulatory agencies and municipalities originally collected for compliance or local characterization, which allowed systematic assessment of seasonal patterns over a wide region. Long term mean concentration for most parameters in most streams was higher during storm discharges than during dry weather flows to at least 95 percent confidence in 20 of 45 comparative evaluations, and lower statistical confidence in 22 other comparisons. Some regional differences emerged: in four evaluated streams in the San Francisco Bay Area, total concentration of lead, copper and zinc were lower during dry weather than during storm flows to at least 99.9 percent confidence, with only one exception; while the other four evaluated California streams showed the same tendency, but to much lower statistical confidence.     

A roadmap for the conservation of freshwater mussels in Europe

Europe has a long history of human pressure on freshwater ecosystems. As pressure continues to grow and new threats emerge, there is an urgent need for conservation of freshwater biodiversity and its ecosystem services. However, whilst some taxonomic groups, mainly vertebrates, have received a disproportionate amount of attention and funds, other groups remain largely off the public and scientific radar. Freshwater mussels (Bivalvia, Unionida) are an alarming example of this conservation bias and here we point out six conceptual areas that need immediate and long-term attention: knowledge, threats, socioeconomics, conservation, governance and education. The proposed roadmap aims to advance research, policy and education by identifying the most pressing priorities for the short- and long-term conservation of freshwater mussels across Europe.     

Leak detection of hydrogen–natural gas mixtures in pipes using the characteristics method of specified time intervals

This paper presents a technique for detection and location of leaks in a single pipe, by means of transient analysis, of hydrogen–natural gas mixtures flows. The method uses transient pressure waves initiated by the sudden closure of a downstream shut-off valve. The presence of a leak in a pipe partially reflects these pressure waves and allows for the location of the leak. Pressure waves are governed by two coupled non-linear, hyperbolic partial differential equations with pressure dependent coefficients. The fluid pressure and velocity are considered as two principal dependent variables. To determine the leak location, the mathematical formulation has been solved by the characteristics method of specified time intervals. The computed results describe the influence of the leak on pressure time-history and the effect of hydrogen mass fraction in the mixture on the leak discharge behaviour. It was found that transient pressure is much important in the case of hydrogen than that in the case of natural gas.     

Enhanced multi-metal extraction with EDDS of deficient and excess dosages under the influence of dissolved and soil organic matter

This study investigated the influence of dissolved and soil organic matter on metal extraction from an artificially contaminated soil. With high concentration of DOM, the extraction of Cu, Zn and Pb was enhanced by forming additional metal-EDDS complexes under EDDS deficiency. However, the enhancement of metal extraction under EDDS excess was probably due to the soil structure being disrupted owing to humic acid enhanced Al and Fe dissolution, which induced more metals dissolving from the soils. Fulvic acid was found to enhance metal extraction to a greater extent compared with humic acid because of its high content of the carboxylic functional group. Cu extraction from the soil with high organic matter content using EDDS was the lowest due to the high binding affinity of Cu to SOM, whereas Zn extraction became the highest because of a preference for EDDS to extract Zn due to the high stability constant of ZnEDDS.     

Influences of redox transformation, metal complexation and aggregation of fulvic acid and humic acid on Cr(VI) and As(V) removal by zero-valent iron

This study investigated the removal kinetics and mechanisms of Cr(VI) and As(V) by Fe(0) in the presence of fulvic acid (FA) and humic acid (HA) by means of batch experiments. The focus was on the involvements of FA and HA in redox reactions, metal complexation, and iron corrosion product aggregation in the removal of Cr(VI) and As(V) removal by Fe(0). Synthetic groundwater was used as the background electrolyte to simulate typical groundwater. The results showed faster Cr(VI) removal in the presence of HA compared to FA. Fluorescence spectroscopy revealed that no redox reaction occurred in the FA and HA. The results of the speciation modeling indicate that the free Fe(II) concentration was higher in the presence of HA, resulting in a higher removal rate of Cr(VI). However, the removal of As(V) was inhibited in the HA solution. Speciation modeling showed that the concentration of dissolved metal-natural organic matter (metal-NOM) complexes significantly affected the aggregation of the iron corrosion products which in turn affected the removal of As(V). The aggregation was found to be induced by gel-bridging of metal-NOM with the iron corrosion products. The effects of metal-NOM on the aggregation of the iron corrosion products were further confirmed by TEM studies. Larger sizes of iron corrosion products were formed in the FA solution compared to HA solution. This study can shed light on understanding the relationships between the properties of NOM (especially the content of metal-binding sites) and the removal of Cr(VI) and As(V) by Fe(0).     

Mercury species of sediment and fish in freshwater fish ponds around the Pearl River Delta, PR China: human health risk assessment

This study investigated total mercury (THg) and methylmercury (MeHg) concentrations in five species of freshwater fish and their associated fish pond sediments collected from 18 freshwater fish ponds around the Pearl River Delta (PRD). The concentrations of THg and MeHg in fish pond surface sediments were 33.1-386 ng g(-1) dry wt and 0.18-1.25 ng g(-1) dry wt, respectively. The age of ponds affected the surface sediment MeHg concentration. The vertical distribution of MeHg in sediment cores showed that MeHg concentrations decreased with increasing depth in the top 10 cm. In addition, a significant correlation was observed between %MeHg and DNA from Desulfovibrionacaea or Desulfobulbus (p<0.05) in sediment cores. Concentrations of THg and MeHg in fish muscles ranged from 7.43-76.7 to 5.93-76.1 ng g(-1) wet wt, respectively, with significant linear relationships (r=0.97, p<0.01, n=122) observed between THg and MeHg levels in fish. A significant correlation between THg concentrations in fish (herbivorous: r=0.71, p<0.05, n=7; carnivorous: r=0.77, p<0.05, n=11) and corresponding sediments was also obtained. Risk assessment indicated that the consumption of largemouth bass and mandarin fish would result in higher estimated daily intakes (EDIs) of MeHg than reference dose (RfD) for both adults and children.     

Significance of metal exchange in EDDS-flushing column experiments

Chelating agents have been widely studied for extracting heavy metals from contaminated soils, and the effectiveness of EDDS ([S,S]-ethylene-diamine-disuccinic acid) has aroused extensive attention because of its biodegradability in the natural environment. However, in the course of EDDS-flushing, metal exchange of newly extracted metal-EDDS complexes with other sorbed metals and mineral cations may result in metal re-adsorption on the soil surfaces. Therefore, this study investigated the relative significance of metal exchange under different travel distances of chelant complexes, characteristics of soil contamination, and solution pH in the column experiments. As a result of metal exchange, the elution of Zn and Pb was retarded and the cumulative extraction was lower than those of Ni and Cu, especially over a longer travel distance. Compared with the field-contaminated soils, the effects of metal exchange were even more substantial in the artificially contaminated soil because of a greater amount of extractable metals and a larger proportion of weakly bound fractions. By contrast, metal exchange was insignificant at pH 8, probably due to less adsorption of metal-EDDS complexes. These findings highlight the conditions under which metal exchange of metal-EDDS complexes and the resulting impacts are more significant during EDDS-flushing.     

Zero-valent iron and iron oxide-coated sand as a combination for removal of co-present chromate and arsenate from groundwater with humic acid

The combination of zero-valent iron (Fe⁰) and iron oxide-coated sand (IOCS) was used to remove Cr(VI) and As(V) from groundwater in this study. The efficiency and the removal mechanism of Cr(VI) and As(V) by using this combination, with the influence of humic acid (HA), were investigated using batch experiments. Results showed that, compared to using Fe⁰ or IOCS alone, the Fe⁰-IOCS can perform better on the removal of both Cr(VI) and As(V). Metal extraction studies showed that As(V) was mainly removed by IOCS and iron corrosion products while Cr(VI) was mainly removed by Fe⁰ and its corrosion products. Competition was found between Cr(VI) and As(V) for the adsorption sites on the iron corrosion products. HA had shown insignificant effects on Cr(VI) removal but some effects on As(V) removal kinetics. As(V) was adsorbed on IOCS at the earlier stage, but adsorbed/coprecipitated with the iron corrosion products at the later stage.