Displaying in the dark: light-dependent alternative mating tactics in the Alpine newt

Environment plays a major role for determining the kind of courtship behaviours or alternative mating tactics employed, but the effect of physical variables on fitness has received little attention. The Alpine newt courts during both day and night times and exhibits a complex suite of behaviours involving olfactory, visual and tactile cues. Displaying in both dark and light conditions may increase the number of mating opportunities and alleviate predation risk, but the frequency and efficacy of the various tactics deployed may vary across light conditions, leading males to vary their use of these tactics across different light regimes. To test this hypothesis, we video-recorded sexual encounters at two light intensities in a controlled experimental design. When courting in the dark, males used comparatively more olfactory rather than visual displays. They also relied more on positive feedback from the female before releasing a spermatophore for her to pick up. The particular mix of tactics used under each light condition is likely to be adaptive because in the dark (1) visual communication is hampered, making olfactory displays possibly more effective and (2) males depositing spermatophores are more likely to lose fertilizations to competitors. Mating in light and dark conditions has similar reproductive payoffs, which shows that displaying in the dark is not detrimental and may even be advantageous if predation risk is reduced at night. These results confirm the importance of taking into account physical variables to understand the evolution of sexual communication in animals.     

Options for water storage and rainwater harvesting to improve health and resilience against climate change in Africa

West and East Africa experience high variability of rainfall that is expected to increase with climate change. This results in fluctuations in water availability for food production and other socioeconomic activities. Water harvesting and storage can mitigate the adverse effects of rainfall variability. But past studies have shown that when investments in water storage are not guided by environmental health considerations, the increased availability of open water surface may increase the transmission of water-related diseases. This is demonstrated for schistosomiasis associated with small reservoirs in Burkina Faso, and for malaria in Ethiopia around large dams, small dams, and water harvesting ponds. The concern is that the rush to develop water harvesting and storage for climate change adaptation may increase the risk for already vulnerable people, in some cases more than canceling out the benefits of greater water availability. Taking health issues into account in a participatory approach to planning, design, and management of rainwater harvesting and water storage, as well as considering the full range of water storage options would enable better opportunities for enhancing resilience against climate change in vulnerable populations in sub-Saharan Africa.     

Applicability of a continuous-flow system inner-coated with S-doped titania for the photocatalysis of dimethyl sulfide at low concentrations

The present study investigated the photocatalytic activity of an S-doped TiO₂ photocatalyst with regards to dimethyl sulfide degradation under visible-light irradiation, along with its deactivation and reactivation. The dimethyl sulfide conversion was between 85% and 93% for the lowest relative humidity range (10–20%) and close to 100% for the two higher relative humidity ranges (45–55% and 80–90%). The conversion was also close to 100% for the two lowest input concentrations (0.039 and 0.195 ppm), while it was between 91% and 96% at 3.9 ppm and between 85% and 90% at 7.9 ppm. In contrast to the input concentration dependences on conversion, the calculated degradation rates increased as input concentrations increased. The dimethyl sulfide conversion at low concentrations (≤0.39 ppm), which are associated with non-occupational inn occurring. However, catalyst deactivations were observed during the photocatalytic process whdoor air quality issues, was up to nearly 100% for long time periods (at least 603 h), without any significant catalyst deactivatioen higher concentrations (3.9 and 7.8 ppm) were used. The photocatalyst, reactivated by using two types of air (dried and humidified) under visible-light irradiation, did not regain all of its initial activities. Sulfate groups were qualitatively identified as the reaction products on the photocatalyst surface. In addition, gaseous byproducts, quantitatively determined, included dimethyl disulfide, methanol, and SO₂. It is noteworthy that the peak concentration of dimethyl disulfide (0.79 ppm = 790 ppb), generated over the photocatalytic process with the highest dimethyl sulfide input concentration, exceeded the odor threshold value of 0.1–3.6 ppb for dimethyl disulfide.     

Determination of seventeen endocrine disruptor compounds and their spatial and seasonal distribution in Ria Formosa Lagoon (Portugal)

In spite of its outstanding ecological and touristic importance the Ria Formosa Lagoon shows signs of anthropogenic pollution. Nonetheless, until the present survey no studies had ever documented the measurement of natural and pharmaceutical estrogens (17β-estradiol, estrone, and 17α-ethynylestradiol), xenoestrogenic industrial pollutants (4-octylphenol, 4-nonylphenol, and their mono and diethoxylates and bisphenol A), phytoestrogens (formononetin, biochanin A, daidzein, genistein), and sitosterol in this area. The 17 compounds measured herein are known as endocrine disrupters (EDCs) and act over the endocrine system even in few amounts (ng L^?1–μg L^?1). Thus to conclude about the influx of EDCs in the lagoon, water samples were taken every 2 months, during 1 year (2010), in low tide at nine sites distributed along the coastline. Water samples (1 L) were preconcentrated in the Oasis HLB cartridges and cleaned in silica cartridges before their analysis by GC-MS. Data showed the ubiquitous presence of potentially hazardous amounts of estrogens (particularly of ethynylestradiol, up to 24.3 ng L^?1), nonylphenol (up to 547 ng L^?1), and sitosterol (up to 12,300 ng L^?1), mainly in summer, suggesting that the increase of the local number of inhabitants (tourists), the rise of the water temperature (up to 26 °C), and the blooming of local flora may interfere with the water quality parameters. This makes the lagoon a potential model to study. Taking into account the data, it was concluded that there are conditions for the occurrence of endocrine disruption in aquatic animals, even in areas included in the natural park of the Formosa. Besides, both the high amounts of un-ionized ammonia (up to 0.3 mg L^?1) and phosphates (up to 1.6 mg L^?1) my pose risks for local fauna and humans.     

Feasibility of a tandem photocatalytic oxidation–adsorption system for removal of monoaromatic compounds at concentrations in the sub-ppm-range

Unlike previous photocatalytic oxidation (PCO) studies incorporated with adsorption, this study investigates the feasibility of applying a tandem PCO-adsorption hybrid technique regarding low-level monoaromatic compound removal. The PCO efficiencies decreased as the hydraulic diameter (HD) increased. A PCO reactor of a medium HD size was selected for further experiments. Under conditions relevant to the use of the PCO system, the CO level measured during the PCO process was minimal in comparison to indoor CO levels. Trace level formations of formaldehyde and acetaldehyde were observed during the photocatalytic process, but these compounds were undetectable at the activated carbon unit outlet. The degradation efficiencies, obtained from the PCO unit, exhibited a dependence on both the inlet concentration (IC) and relative humidity (RH), whereas those from the PCO-adsorption hybrid system did not. Under specific conditions, the PCO unit presented a high degradation efficiency of close to, or exceeding 90%, in regards to ethyl benzene, o-xylene, and m,p-xylene. However, the benzene air concentrations, after being treated by the PCO unit, substantially exceeded the USEPA inhalation reference concentration guideline of 30 μg m⁻³ (corresponding to 0.01 ppm). In contrast, the PCO-adsorption hybrid system presented a high removal efficiency of close to 100% regarding all compounds, regardless of the IC or RH range. Consequently, it is suggested that the PCO-adsorption hybrid system has a synergistic advantage of photocatalysis and adsorption in regards to the BTEX elimination process.     

The anthropogenic atmospheric elements fraction: A new interpretation of elemental deposits on tree barks

The superficial deposit on the bark surface of several trees (mainly Fraxinus excelsior L.) was sampled in the experimental station of the university campus in Grenoble (France). Its composition was studied by scanning electron microscopy–energy dispersive X-ray emission (SEM–EDX) and, after digestion, by inductively coupled plasma-mass spectrometry (ICP-MS). The deposit was composed of 81.3% ± 7.4 organic matter, 9.4% ± 4.9 of geogenic minerals issued from the atmosphere (atmospheric geogenic fraction: AGF) and 9.3% ± 2.7 of a mixture of elements which was called anthropogenic atmospheric elements fraction (AAEF). The SEM–EDX analysis showed the presence of particles of geogenic compounds such as different types of silicates, phosphates, carbonates, sulphates, oxides and also particles of metals such as iron or of alloys of Fe–Zn, Fe–Ni, Ni–Cr and Ca sulphates or phosphates. Typical spheres of “fly ashes” composed of pure iron or Al-silicates were detected. Using the SEM–EDX analysis of the deposit and the average local soil composition, an empiric formula for the AGF (without polluting elements) was chosen, which presented a clear analogy with the global formula of the upper continental crust. In the same way, a formula for the pure organic matter fraction was chosen. Withdrawing the elements corresponding to these two fractions allows a tentative estimation of the content of the AAEF which was supposed to better represent the elemental anthropogenic contamination issued from the atmosphere. In the station, most of Sb, Cd, Sn, Pb, Cu, V and Zn were found in the AAEF. This AAEF composition was compared to that of the deposit in a highway tunnel where Pb and Cu were at a very high level. The meaning and the limits of the AAEF concept were critically discussed.     

Monitoring and assessing processes of organic chemicals removal in constructed wetlands

Physical, chemical and biological processes interact and work in concert during attenuation of organic chemicals in wetland systems. This review summarizes the recent progress made towards understanding how the various mechanisms attributed to organic chemicals removal interact to form a functioning wetland. We also discuss the main degradation pathways for different groups of contaminants and examine some of the key characteristics of constructed wetlands that control the removal of organic chemicals. Furthermore, we address possible comprehensive approaches and recent techniques to follow up in situ processes within the system, especially those involved in the biodegradation processes.     

Differential global profiling as a new analytical strategy for revealing micropollutant treatment by-products: application to ethinylestradiol and chlorination water treatment

The detection and structural elucidation of micropollutants treatment by-products are major issues to estimate efficiencies of the processes employed for drinking water production versus endocrine disruptive compounds contamination. This issue was mainly investigated at the laboratory scale and in high concentration conditions. However, potential by-products generated after chlorination can be influenced by the dilution factor employed in real conditions. The present study proposes a new methodology borrowed to the metabolomic science, using liquid chromatography coupled to high-resolution mass spectrometry, in order to reveal potential chlorination by-products of ethinylestradiol in spiked real water samples at the part-per-billion level (5 μg L⁻¹). Conventional targeted measurements first demonstrated that chlorination with sodium hypochlorite (0.8 mg L⁻¹) led to removals of ethinylestradiol over 97%. Then, the developed differential global profiling approach permitted to reveal eight chlorination by-products of EE2, six of them being described for the first time. Among these eight halogenated compounds, five have been structurally identified, demonstrating the potential capabilities of this new methodology applied to environmental samples.     

Defining Chlorophyll-a Reference Conditions in European Lakes

The concept of “reference conditions” describes the benchmark against which current conditions are compared when assessing the status of water bodies. In this paper we focus on the establishment of reference conditions for European lakes according to a phytoplankton biomass indicator—the concentration of chlorophyll-a. A mostly spatial approach (selection of existing lakes with no or minor human impact) was used to set the reference conditions for chlorophyll-a values, supplemented by historical data, paleolimnological investigations and modelling. The work resulted in definition of reference conditions and the boundary between “high” and “good” status for 15 main lake types and five ecoregions of Europe: Alpine, Atlantic, Central/Baltic, Mediterranean, and Northern. Additionally, empirical models were developed for estimating site-specific reference chlorophyll-a concentrations from a set of potential predictor variables. The results were recently formulated into the EU legislation, marking the first attempt in international water policy to move from chemical quality standards to ecological quality targets.     

Synthesis of zeolite from waste fly ash for adsorption of CO2

Zeolitic sorbents for CO₂ adsorption were prepared from waste coal fly ash (FA) through hydrothermal treatment at various ratios of NaOH/FA and NaAlO₂/FA, including an initial alkali fusion step. The fusion step decomposed the fly ash into very small amorphous particulate zeolite forms. The fly ash was converted to Na-P1 type with a NaOH/FA ratio of 0.5 and Na-A type with a NaAlO₂/FA ratio of 0.53. The product properties were affected by the reaction temperature: Na-P1 and Na-A types were formed at 100°C. Temperatures above 140°C led to the formation of more sodalite because of the redissolving and recrystallization of zeolite crystals. Alkali metal and alkaline earth metal cations were impregnated in the synthesized Na-P1 and Na-A zeolite through an ion-exchange method. The completed zeolitic sorbents were applied to the adsorption of low-level CO₂. As a result of the experiments, calcium ions were found to be the best for CO₂ adsorption owing to their electrostatic behavior and acid-base interaction.