Influence of Potamogeton crispus growth on nutrients in the sediment and water of Lake Tangxunhu

An incubation experiment was performed on Potamogeton crispus (P. crispus) using sediment collected from Lake Tangxunhu in the center of China, in order to determine the effects of plant growth on Fe, Si, Cu, Zn, Mn, Mg, P, and Ca concentrations in the sediments and overlying waters. After 3 months of incubation, Ca, Mg, and Si concentrations in the water column were significantly lower, and P and Cu concentrations were significantly higher than in unplanted controls. The effect of P. crispus growth on sediment pore waters and water-extractable elements varied. Concentrations of Ca, Mg, Si, Fe, Cu, and Zn were significantly higher, and P was significantly lower, than in pore waters of the control. Water-extracted concentrations of Fe, Mg, and Si in the sediments were lower, and P was higher, than in the control. Presence of P. crispus generally enhanced concentration gradients of elements between pore waters and overlying waters but not for P. The growth of P. crispus was associated with an increase in water pH and formation of root plaques, resulting in complex effects on the sediment nutritional status

Metal adsorption by quasi cellulose xanthogenates derived from aquatic and terrestrial plant materials

The FTIR spectra, SEM-EDXA and copper adsorption capacities of the raw plant materials, alkali treated straws and cellulose xanthogenate derivatives of Eichhornia crassipes shoot, rape straw and corn stalk were investigated. FTIR spectra indicated that of the three plant materials, the aquatic biomass of Eichhornia crassipes shoot contained more O-H and C=O groups which accounted for the higher Cu²⁺ adsorption capacities of the raw and alkali treated plant material. SEM-EDXA indicated the incorporation of sulphur and magnesium in the cellulose xanthogenate. The Cu²⁺ adsorption capacities of the xanthogenates increased with their magnesium and sulphur contents. However more copper was adsorbed than that can be explained by exchange of copper with magnesium. Precipitation may contribute to the enhanced uptake of copper by the cellulose xanthogenate

Self-concept mediates the relationships between childhood traumatic experiences and adolescent depression in both clinical and community samples

Background: Childhood trauma is a pivotal risk factor for adolescent depression. While the association between childhood trauma and depression is well-established, the mediating role of self-concept has not been acknowledged. Specifically, limited attention has been paid to how childhood maltreatment impacts adolescent depression through physical and social self-concept, both in clinical and community samples. This study aims to investigate how distinct and cumulative childhood trauma affects adolescent depression, as well as the potential mediating role of self-concept in their relationships. Methods: We recruited 227 depressed adolescents (dataset 1, 45 males, age = 15.34 ± 1.96) and 574 community adolescents (dataset 2, 107 males, age = 16.79 ± 0.65). Each participant was assessed on five subtypes of childhood trauma severity, cumulative trauma index, physical and social self-concept, and depression. Mediation models were tested separately in the clinical and community samples. Results: Clinically depressed adolescents experienced a higher level of trauma severity, a greater number of trauma subtypes, and had lower levels of physical and social self-concept compared to community adolescents. Analyses on childhood trauma severity and cumulative trauma index jointly indicated that physical and social self-concept played mediation roles in the relationships between childhood trauma experiences and depression. Moreover, the mediating effects of self-concept were stronger in depressed adolescents when compared to community samples. Conclusions: Our findings suggest that physical and social self-concept play mediating roles in the pathway linking childhood trauma and adolescent depression, particularly in clinically depressed individuals

Diversity of NC10 bacteria associated with sediments of submerged Potamogeton crispus (Alismatales: Potmogetonaceae)

Background The nitrite-dependent anaerobic methane oxidation (N-DAMO) pathway, which plays an important role in carbon and nitrogen cycling in aquatic ecosystems, is mediated by “Candidatus Methylomirabilis oxyfera” (M. oxyfera) of the NC10 phylum. M. oxyfera-like bacteria are widespread in nature, however, the presence, spatial heterogeneity and genetic diversity of M. oxyfera in the rhizosphere of aquatic plants has not been widely reported. Method In order to simulate the rhizosphere microenvironment of submerged plants, Potamogeton crispus was cultivated using the rhizobox approach. Sediments from three compartments of the rhizobox: root (R), near-rhizosphere (including five sub-compartments of one mm width, N1–N5) and non-rhizosphere (>5 mm, Non), were sampled. The 16S rRNA gene library was used to investigate the diversity of M. oxyfera-like bacteria in these sediments. Results Methylomirabilis oxyfera-like bacteria were found in all three sections, with all 16S rRNA gene sequences belonging to 16 operational taxonomic units (OTUs). A maximum of six OTUs was found in the N1 sub-compartment of the near-rhizosphere compartment and a minimum of four in the root compartment (R) and N5 near-rhizosphere sub-compartment. Indices of bacterial community diversity (Shannon) and richness (Chao1) were 0.73–1.16 and 4–9, respectively. Phylogenetic analysis showed that OTU1-11 were classified into group b, while OTU12 was in a new cluster of NC10. Discussion Our results confirmed the existence of M. oxyfera-like bacteria in the rhizosphere microenvironment of the submerged plant P. crispus. Group b of M. oxyfera-like bacteria was the dominant group in this study as opposed to previous findings that both group a and b coexist in most other environments. Our results indicate that understanding the ecophysiology of M. oxyfera-like bacteria group b may help to explain their existence in the rhizosphere sediment of aquatic plant

Synthesis, Characterization, and Evaluation of Boron-Doped Iron Oxides for the Photocatalytic Degradation of Atrazine under Visible Light

Photocatalytic degradation of atrazine by boron-doped iron oxides under visible light irradiation was investigated. In this work, boron-doped goethite and hematite were successfully prepared by sol-gel method with trimethylborate as boron precursor. The powders were characterized by XRD, UV-vis diffuse reflectance spectra, and porosimetry analysis. The results showed that boron doping could influence the crystal structure, enlarge the BET surface area, improve light absorption ability, and narrow their band-gap energy. The photocatalytic activity of B-doped iron oxides was evaluated in the degradation of atrazine under the visible light irradiation, and B-doped iron oxides showed higher atrazine degradation rate than that of pristine iron oxides. Particularly, B-doped goethite exhibited better photocatalytic activity than B-doped hematite

Synthesis and Characterization of Mn–C–Codoped TiO2 Nanoparticles and Photocatalytic Degradation of Methyl Orange Dye under Sunlight Irradiation

Novel visible-light-active Mn–C–TiO2 nanoparticles were synthesized by modified sol-gel method based on the self-assembly technique using polyoxyethylenes orbitan monooleate (Tween 80) as template and carbon precursor and manganese acetate as manganese precursor. The samples were characterized by XRD, FTIR, UV-vis diffuse reflectance, XPS, and laser particle size analysis. The XRD results showed that Mn–C–TiO2 sample exhibited anatase phase and no other crystal phase was identified. High specific surface area, small crystallite size, and small particle size distribution could be obtained by manganese and carbon codoped and Mn–C–TiO2 exhibited greater red shift in absorption edge of samples in visible region than that of C–TiO2 and pure TiO2. The photocatalytic activity of synthesized catalyst was evaluated by photocatalytic oxidation of methyl orange (MO) solution under the sunlight irradiation. The results showed that Mn–C–TiO2 nanoparticles have higher activity than other samples under sunlight, which could be attributed to the high specific surface area, smaller particle size, and lower band gap energy

Photodecomposition of Organic Phosphorus in Aquatic Solution under Solar Irradiation with Nitrate: Kinetics and Influencing Water Parameters

The transformation of organic phosphorus plays an important role in the phosphorus cycle in the natural environment. In this study, a series of laboratory-based experiments were conducted to address the influence of nitrate (NO3-) photochemical activity on the transformation of methyl parathion under solar irradiation. It is demonstrated that the photodecomposition of methyl parathion by NO3- obeys pseudo-first-order reaction kinetics, with the photodecomposition rate increasing with NO3- concentration. The photodecomposition rates of methyl parathion by NO3- were strongly influenced by pH, concentration of humic acid and Fe 31. Higher concentrations of Fe 31 and lower concentrations of humic acid accelerated the photodegradation induced by NO3-. Moreover, compared to alkaline media the acidic media can enhance the rate of methyl parathion degradation. Formation of the hydroxyl radical (center dot OH) was identified through the measurement of photoluminescence spectra (PL) using terephthalic acid as the trapping molecule. The primary transformation pathways of methyl parathion in the presence of NO3- under solar irradiation were proposed through the qualitative and quantitative analysis of byproducts. Intermediates, such as paraoxon, 4-nitrophenol and orthophosphate, were identified, and a mineralization pathway from methyl parathion to orthophosphate was proposed. (C) 2016 American Institute of Chemical Engineer

Controlled-release urea encapsulated by ethyl cellulose/butyl acrylate/vinyl acetate hybrid latex

Fertilizer encapsulation through polymer membranes can reduce fertilizer losses and minimize environmental pollution. In this paper, an emulsion of ethyl cellulose (EC)/vinyl acetate (VAc)/butyl acrylate (BA) was successfully prepared by pre-emulsified semi-continuous seed emulsion polymerization. EC/BA/VAc films showed biodegradability. The influence of the EC content on the properties of EC/BA/VAc films was also investigated by DSC, a water absorbency analysis, etc. Controlled-release urea encapsulated by EC/BA/VAc latex was prepared in a film coating machine and conformed to the standards for slow-release fertilizers of the Committee of European Normalization. The release of urea from controlled-release urea encapsulated by EC/BA/VAc latex containing 0%, 5%, 10%, and 15% EC was 75.1%, 65.8%, 70.1% and 84.1%, respectively, after 42 days, and controlled-release urea encapsulated by EC/BA/VAc latex (5% EC) had the best controlled-release ability. Therefore, controlled-release urea encapsulated by EC/BA/VAc latex has many potential applications in agricultural industry