Novel magnetic carbonaceous bio-char was hydrothermal prepared from microalgae under different loadings of iron and its structures and surface chemistry were characterized with Fourier transform infrared (FTIR), X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), and nitrogen adsorption-desorption isotherm (BET). The morphology of bio-char changed from sheet to particle as iron loading increased and its surface area also increased. When 3.0 g of dried microalgae and 6.0 mmol iron salt ((NH₄)₂SO₄·FeSO₄·6H₂O) were mixed and treated, the obtained bio-char possessing the highest amount of oxygen-containing functional groups resulted in the best adsorption performance on tetracycline (TC). This adsorption process was fitted to Langmuir adsorption isotherm and the maximum adsorption capacity was 95.86 mg/g, which is higher than other bio-char reported. The iron loading contributed to the higher adsorption capacity of bio-char, which may be due to three factors, the high surface area, more hydrogen bonding, and bridging effects of the structural Fe for TC. Our data suggest that bio-char may have more important role in stabilization of pollutants in the environment.

Ecological remediation is an important measure for the protection of lake water quality in removing nutrients, such as nitrate (NO₃⁻). In this study, four bioremediation processes (bare sediment, immobilized nitrogen cycling bacteria (INCB) added, Elodea nuttallii added, E. nuttallii-INCB assemblage) were operated at a lab to elucidate the effect of macrophyte appearance and INCB addition on NO₃⁻removal and achieve the optimal processes for biomediation.¹⁵ N-NO₃solution was added to microcosms to identify the key nitrogen transformation processes responsible for NO₃⁻removal. Results showed that nitrate removal was significantly enhanced after the addition of INCB and E. nuttallii. In the treatments with INCB added, E. nuttallii added, and INCB and E. nuttallii-INCB assemblage, nitrate removal ratio achieved 94.74, 98.76, and 99.15 %, respectively. In contrast, only 23.47 % added nitrate was removed in the control. Plant uptake and denitrification played an important role in nitrogen removal. The water quality was substantially improved by the addition of INCB and macrophyte that can accelerate denitrification and promote nitrogen assimilation of plants. The results indicated that plant uptake and microbial denitrification were key processes for nitrate removal.

Hydroponic experiments were conducted with rice seedlings (Oryza sativa L. cv. ND1) exposed to methylene blue (MB) to investigate the accumulation of hydrogen peroxide (H₂O₂) and activities and gene expression of antioxidant enzymes. Results showed that a linear decrease in relative growth rate and water use efficiency was observed with rice seedlings with increasing MB concentrations. MB-induced accumulation of H₂O₂was evident in both roots and shoots. The activities of antioxidative enzymes were analyzed and found to be different at different MB treatment concentrations. The activities of enzymes related to the ascorbate-glutathione cycle were more sensitive to MB treatments than other antioxidative enzymes. Transcript level, by real-time quantitative PCR, of antioxidative enzymes showed that the analyzed genes were differently expressed during different MB concentrations in both roots and shoots. The isoform analysis of superoxide dismutase (SOD) gene showed that the expressions of Cu/ZnSOD and MnSOD were relatively constant, where significant upregulation of FeSOD was observed with rice seedlings exposed to high MB concentrations. Furthermore, the expression of CAT, POD, and MDHAR genes responded biphasically to MB treatments by showing negligible changes at 1.56–15.63 μM MB and significant induction at 31.36–62.52 μM MB. The expression of GR, APX, and DHAR genes showed a remarkable induction to MB. Our results suggest that on transcription level, and in accordance with enzymatic responses, enzymes of GR, APX, and DHAR play central role in the H₂O₂detoxification in rice seedlings under MB exposure.

Biodegradation of naphthalene by Ralstonia eutropha (also known as Cupriavidus necator) in a packed-bed airlift reactor with net draft tube (PBALR-nd) was studied; the Kissiris pieces were the packing material. The reactor hydrodynamics has been characterized under abiotic conditions and the dependencies of the superficial gas velocity (UG) on the gas holdup (εG), liquid mixing time, and mass transfer coefficient were determined. The improving role of the net draft tube in this small column reactor (height 42 cm, ID 5 cm) was confirmed. The flow regime was described using the εGα UG ⁿ expression, and bubbly flow was observed in PBALR-nd at UG< 2.83 cm/s. In the second step of the present work, the kinetics of biodegradation was modeled using the Haldane and Aiba equations. The fitting of the experimental results to the models were done according to the nonlinear least square regression technique. The biokinetic constants (qₘ, Kₛ, and Kᵢ) were estimated and qₘas the specific biodegradation rate was equaled to 0.415 and 0.24 mgₙₐₚₕ./mgcₑₗₗ h for the Haldane and Aiba equations, respectively. The goodness of fit reported as R²and root-mean-square error (RMSE) showed the adequate fitness of the Haldane and Aiba models in predicting naphthalene biodegradation kinetics. On the basis of the HPLC results, a hypothetical pathway for the biodegradation was presented.

As it flows through a dense steelmaking area, the Fensch River does transport iron-rich particles and colloids, displaying high contents in metallic contaminants (Zn, Cr, Pb, Cu, Ni, and As). Chemical analysis using inductively coupled plasma mass spectrometry (ICP-MS) was carried out on three compartments—waters, suspended materials, and sediments—along the river linear. The variations of metallic trace element concentrations along the river were shown to be partially related to external inputs (industrial and domestic wastewaters and urban surfaces leaching). However, some discrepancies of element partitioning were evidenced. Pb, Cu, and Mn tend to concentrate in suspended particulate and in dissolved fraction, while Cr and As follow the trend of Fe and concentrate within sediments of the most downstream station, just before the junction with Moselle waters. Zn appears strongly associated to iron-rich particles, resulting in a decrease of its concentration in waters for the last station. Along the Fensch linear, the variation of metal partitioning between water and particulate phases is accompanied with strong modifications of the nature and mineralogy of iron-rich particles, as evidenced by microanalyses using electron and X-ray beams. The combination of bulk analyses using ICP-MS and microanalyses applied to the three compartments allowed us to propose a three-step process “settling–weathering–resuspension” to explain Zn partitioning.

Chlordecone is an organochlorine insecticide that has been widely used to control banana weevil in the French West Indies. As a result of this intense use, up to 20,000 ha are contaminated by this insecticide in the French West Indies, and this causes environmental damage and health problems. A scenario of exposure was drawn by French authorities, based on land usage records. Many efforts have been made to monitor the occurrence of chlordecone and its main metabolites using different analytical methods, including GC, GC/MS, LC/MS, and NIRS. Although these different methods allow for the detection and quantification of chlordecone from soils, none of them estimate the bottleneck caused by extraction of this organochlorine from soils with high adsorption ability. In this study, we used¹³C₁₀-chlordecone as a tracer to estimate chlordecone extraction yield and to quantify chlordecone in soil extracts based on the¹³C/¹²C isotope dilution. We report the optimization of¹³C₁₀-chlordecone extraction from an Andosol. The method was found to be linear from 0.118 to 43 mg kg⁻¹in the Andosol, with an instrumental detection limit estimated at 8.84 μg kg⁻¹. This method showed that chlordecone ranged from 35.4 down to 0.18 mg kg⁻¹in Andosol, Nitisol, Ferralsol, and Fluvisol soil types. Traces of the metabolite β-monohydrochlordecone were detected in the Andosol, Nitisol, and Ferralsol soil samples. This last result indicates that this method could be useful to monitor the fate of chlordecone in soils of the French West Indies.

Candle composition is expected to influence the air pollutants emissions, possibly leading to important differences in the emissions of volatile organic compounds and polycyclic aromatic hydrocarbons. In this regard, the purity of the raw materials and additives used can play a key role. Consequently, in this work emission factors for some polycyclic aromatic hydrocarbons, aromatic species, short-chain aldehydes and particulate matter have been determined for container candles constituted by different paraffin waxes burning in a test chamber. It has been found that wax quality strongly influences the air pollutant emissions. These results could be used, at least at a first glance, to foresee the expected pollutant concentration in a given indoor environment with respect to health safety standards, while the test chamber used for performing the reported results could be useful to estimate the emission factors of any other candle in an easy-to-build standardised environment.

To investigate the spatial and seasonal variations of nitrous oxide (N₂O) fluxes and understand the key controlling factors, we explored N₂O fluxes and environmental variables in high marsh (HM), middle marsh (MM), low marsh (LM), and mudflat (MF) in the Yellow River estuary throughout a year. Fluxes of N₂O differed significantly between sampling periods as well as between sampling positions. During all times of day and the seasons measured, N₂O fluxes ranged from −0.0051 to 0.0805 mg N₂O m⁻² h⁻¹, and high N₂O emissions occurred during spring (0.0278 mg N₂O m⁻² h⁻¹) and winter (0.0139 mg N₂O m⁻² h⁻¹) while low fluxes were observed during summer (0.0065 mg N₂O m⁻² h⁻¹) and autumn (0.0060 mg N₂O m⁻² h⁻¹). The annual average N₂O flux from the intertidal zone was 0.0117 mg N₂O m⁻² h⁻¹, and the cumulative N₂O emission throughout a year was 113.03 mg N₂O m⁻², indicating that coastal marsh acted as N₂O source. Over all seasons, N₂O fluxes from the four marshes were significantly different (p < 0.05), in the order of HM (0.0256 ± 0.0040 mg N₂O m⁻² h⁻¹) > MF (0.0107 ± 0.0027 mg N₂O m⁻² h⁻¹) > LM (0.0073 ± 0.0020 mg N₂O m⁻² h⁻¹) > MM (0.0026 ± 0.0011 mg N₂O m⁻² h⁻¹). Temporal variations of N₂O emissions were related to the vegetations (Suaeda salsa, Phragmites australis, and Tamarix chinensis) and the limited C and mineral N in soils during summer and autumn and the frequent freeze/thaw cycles in soils during spring and winter, while spatial variations were mainly affected by tidal fluctuation and plant composition at spatial scale. This study indicated the importance of seasonal N₂O contributions (particularly during non-growing season) to the estimation of local N₂O inventory, and highlighted both the large spatial variation of N₂O fluxes across the coastal marsh (CV = 158.31 %) and the potential effect of exogenous nitrogen loading to the Yellow River estuary on N₂O emission should be considered before the annual or local N₂O inventory was evaluated accurately.

Development and optimisation of alternative strategies to reduce the use of classic chemical inputs for protection against diseases in vineyard is becoming a necessity. Among these strategies, one of the most promising consists in the stimulation and/or potentiation of the grapevine defence responses by the means of elicitors. Elicitors are highly diverse molecules both in nature and origins. This review aims at providing an overview of the current knowledge on these molecules and will highlight their potential efficacy from the laboratory in controlled conditions to vineyards. Recent findings and concepts (especially on plant innate immunity) and the new terminology (microbe-associated molecular patterns, effectors, etc.) are also discussed in this context. Other objectives of this review are to highlight the difficulty of transferring elicitors use and results from the controlled conditions to the vineyard, to determine their practical and effective use in viticulture and to propose ideas for improving their efficacy in non-controlled conditions.

In this work, principal component analysis/multiple linear regression (PCA/MLR), positive matrix factorization (PMF), and UNMIX model were employed to apportion potential sources of polycyclic aromatic hydrocarbons (PAHs) in surface sediments from middle and lower reaches of the Yellow River, based on the measured PAHs concentrations in sediments collected from 22 sites in November 2005. The results suggested that pyrogenic sources were major sources of PAHs. Further analysis indicated that source contributions of PAHs compared well among PCA/MLR, PMF, and UNMIX. Vehicles contributed 25.1–36.7 %, coal 34.0–41.6 %, and biomass burning and coke oven 29.2–33.2 % of the total PAHs, respectively. Coal combustion and traffic-related pollution contributed approximately 70 % of anthropogenic PAHs to sediments, which demonstrated that energy consumption was a predominant factor of PAH pollution in middle and lower reaches of the Yellow River. In addition, the distributions of contribution for each identified source category were studied, which showed similar distributed patterns for each source category among the sampling sites.