Chlorophyll fluorescence spectral analysis permits detection, monitoring, and evaluation of abiotic stresses upon healthy plants using illumination of a light source in the UV–VIS spectral range. This technique indirectly assesses the amount of physiological stress caused by photosynthetic damage, specifically damage to photosystem II, in plants. The objective of this study was to detect the toxicity of cadmium in maize plants via spectral analysis of chlorophyll fluorescence. The analysis is noninvasive and nondestructive and is used to follow the temporal evolution of changes in the chlorophyll content and physiological state of Zea mays L. seedlings under cadmium stress. Conventional techniques were also used to evaluate the dry matter production and Cd accumulation in plant leaves. Plants exhibited a notable reduction in dry matter production and chlorophyll levels with the administration of increasing doses of Cd in the nutrient solution. The fluorescence analysis was sensitive to changes caused by Cd in maize plants, detecting damage caused by different treatments before visual symptoms were observed. This technique has a practical application and produces rapid results that can be used in the evaluation of Cd-induced stress in plants and the detection of areas contaminated by this element.

A directly amine-functionalized mesoporous silica (AMS) was prepared via an anionic surfactant-mediated synthesis method and used as adsorbents for deep removal of Cu ions from aqueous solution at room temperature. The synthesized AMS had been characterized by X-ray diffraction, nitrogen physisorption measurement, and thermogravimetric analysis. The amine groups prefer to position to the surface of AMS material due to the SN ∼ I mechanism. Copper adsorption process had been studied from both kinetic and equilibrium points of view for AMS material. Experiments proved that the aqueous Cu adsorption rates were fast and adsorption capacity was about 53.3 mg/g.

Many of the environmental problems related to agriculture will still be serious over the next 30 years. However, the seriousness of some of those problems may increase more slowly than in the past or even diminish in other cases (FAO 2002). Agriculture plays two different roles in climate change; on one hand, it suffers from the impact of climate change, on the other hand, it is responsible for 14 % of total greenhouse gases (MMA 2008). Nevertheless, agriculture is also part of the solution, as it is capable of mitigating a significant amount of global emissions, according to the FAO (2001). This paper aims to study the influence of edapho-climate conditions on soil CO2 emissions into the atmosphere. In order to do so, we conducted three field trials in different areas in southern Spain, which have different soil textures and different climate conditions. The results show how interaction between the temperature and rainfall recorded has a greater influence on emissions than each of the factors separately. However, at the same time, the texture of the soil at each of the locations was also found to be the most dominant variable in the gas emission process.

Studies concerning competitive sorption of anions on oxidic materials eligible to be used as soil amendments are crucial for a better understanding of the adsorbent’s effectiveness and ion mobility/availability in the environment. This study evaluated mono-/multi-element adsorption of phosphate and arsenate on aluminum (AMB) and iron mining by-products (IMB; used for comparison) and measured the effect of pH and thermal pretreatments on P and As adsorption on AMB and IMB. We also evaluated whether the desorption of As previously adsorbed on AMB and IMB increases with the addition of increasing doses of P. For adsorption, each adsorbent was reacted at selected pHs with solutions containing As and P individually or in combination. Non-competitive desorption was performed with 30 mmol L⁻¹ NaCl. Arsenate displacement was evaluated by reaction of the adsorbents containing previously adsorbed As with P-containing solutions. The competition between P and As decreased the adsorption of these anions by 2.7 and 23.2 %, respectively. Increasing pH decreased adsorption of both As and P, whereas the thermal pretreatment increased P adsorption by 40 % and As adsorption by 15 %. Phosphate in solution increased As desorption, with each millimoles per kilogram of adsorbed P desorbing as much as 2.3 ± 1.1 mmol kg⁻¹ of As.

Leachable chromium in the incineration fly ash and wastewater sludge has been thermally stabilized by plasma melting at the temperature of 1,773 K. To better understand how chromium is stabilized with the high-temperature treatment, chemical structure of the slags sampled at temperature zones of 1,100–1,700 K has been studied by synchrotron X-ray absorption spectroscopy. The component-fitted X-ray absorption near edge structure spectra of chromium indicate that the main chromium compounds in the sludge and fly ash are Cr(OH)₃, Cr₂O₃, and CrCl₃. A small amount of toxic CrO₃ is also observed in the fly ash. In the plasma melting chamber under the reducing environment, the high-oxidation state chromium is not found. The slags in the plasma melting chamber have much less leachable chromium, which is due to chemical interactions between chromium and SiO₂ in the slags. The existence of the interconnected Cr-O-Si species is observed by refined extended X-ray absorption fine structure spectroscopy. In the Cr₂O₃ phase of the slags, their bond distances, and coordination numbers for the first (Cr-O) and second (Cr-(O)-Cr) shells have insignificant perturbation when experienced with different melting temperatures between 1,300 and 1,700 K. It seems that Cr₂O₃ and chromium encapsulated in the silicate matrix of the slags have relatively much lower leachability. With this concept, to obtain a low chromium leachability slag from the plasma melting process, the residence time of the melting chamber may be decreased, and the slag discharge temperatures may be increased to 1,300 K. This work also exemplifies utilization of molecule-scale data obtained from synchrotron X-ray absorption spectroscopy to reveal how chromium is thermally stabilized in a commercial scale plasma melting process.

Plant growth-promoting rhizobacteria (PGPR) play an important role in the biodegradation of natural and xenobiotic organic compounds in soil. They can also alter heavy metal bioavailability and contribute to phytoremediation in the presence or absence of synthetic metal chelating agents. In this study, the inhibitory effect of Cd2+ and Ni2+ at different concentrations of Ca2+ and Mg2+, and the influence of the widely used chelator EDTA on growth of the PGPR Pseudomonas brassicacearum in a mineral salt medium with a mixture of four main plant exudates (glucose, fructose, citrate, succinate) was investigated. Therefore, the bacteriostatic effect of Cd2+, Ni2+ and EDTA on the maximum specific growth rate and the determination of EC50 values was used to quantify inhibitory impact. At high concentrations of Ca2+ (800 μmol L-1) and Mg2+ (1,250 μmol L-1), only a small inhibitory effect of Cd2+ and Ni2+ on growth of P. brassicacearum was observed (EC50 Cd2+, 18,849 ±â€‰80 μmol L−1; EC50 Ni2+, 3,578 ±â€‰1,002 μmol L−1). The inhibition was much greater at low concentrations of Ca2+ (25 μmol L−1) and Mg2+ (100 μmol L−1) (EC50 Cd2+, 85 ±â€‰0.5 μmol L−1 and EC Ni2+, 62 ±â€‰1.8 μmol L−1). For the chosen model system, a competitive effect of the ions Cd2+ and Ca2+ on the one hand and Ni2+ and Mg2+ on the other hand can be deduced. However, the toxicity of both, Cd2+ and Ni2+, could be significantly reduced by addition of EDTA, but if this chelating agent was added in stoichiometric excess to the cations, it also exhibited an inhibitory effect on growth of P. brassicacearum.

PURPOSE: In order to better understand if the metabolic responses of echinoids could be related to their acid–base status in an ocean acidification context, we studied the response of an intertidal sea urchin species, Paracentrotus lividus, submitted to low pH at two different temperatures. METHODS: Individuals were submitted to control (8.0) and low pH (7.7 and 7.4) at 10°C and 16°C (19 days). The relation between the coelomic fluid acid–base status, the RNA/DNA ratio of gonads and the individual oxygen uptake were studied. RESULTS: The coelomic fluid pH decreased with the aquarium seawater, independently of temperature, but this explained only 13% of the pH variation. The coelomic fluid showed though a partial buffer capacity that was not related to skeleton dissolution ([Mg2+] and [Ca2+] did not differ between pH treatments). There was an interaction between temperature and pH on the oxygen uptake (V O2) which was increased at pH 7.7 and 7.4 at 10°C in comparison with controls, but not at 16°C, indicating an upregulation of the metabolism at low temperature and pH. However, gonad RNA/DNA ratios did not differ according to pH and temperature treatments, indicating that even if maintenance of physiological activities has an elevated metabolic cost when individuals are exposed to stress, they are not directly affected during short-term exposure. Long-term studies are needed in order to verify if gonad production/growth will be affected by low pH seawaters exposure.