Response of the common reed (Phragmites australis) to nutrient enrichment depends on the growth stage and degree of enrichment: A mesocosm experiment.

Human-induced nutrient enrichment is a major stressor in aquatic ecosystems that has resulted in the alteration of ecosystem structures and functions. However, to date, relatively few studies have explored the temporal dynamics of reed biomass and morphological and biochemical traits under different nutrient levels, as well as the phenological pattern. Based on a mesocosm experiment, we monitored the aboveground and underground biomass of reed at the different plant growth stages, along with plant height, ramet and leaf number, leaf length and width, and carbohydrate and nutrient contents in different organs. We found that the significantly different ratio of aboveground to underground biomass was only observed at the late flowering stage between the slight enrichment (S-E) and heavy enrichment (H-E) groups. The start of the fast-growth phase of the aboveground part and underground part was delayed in the higher nutrient enrichment groups. The length of the fast-growth phase of the aboveground part was the same in the medium enrichment (M-E) and H-E groups and longer than that in the S-E group. For the underground part, the longest fast-growth phase was found in the S-E group (105 days), followed by the H-E and M-E groups (46 and 41 days, respectively). As the nutrient level increased, both increased and decreased values were observed for the 29 monitored morphological and biochemical traits, and the magnitude changed with the different growth stages. Moreover, different degrees of nutrient enrichment could differentially enhance or weaken the relationships among the groups between total biomass and the integrated morphological trait, between structural carbohydrate (SC) and total nitrogen (TN) contents, between total organic carbon (TOC) and TN, between total phosphorus (TP) contents, between TOC and SC contents. Our findings highlight a crucial contribution of ambient nutrient supply to temporal variation in plant biomass and phenological, morphological and biochemical traits.

Facile Synthesis of Magnetic Biochar Derived from Burley Tobacco Stems towards Enhanced Cr(VI) Removal: Performance and Mechanism.

In this study, ferric-loaded magnetic burley tobacco stem biochar (MBTS) was synthesized via pyrolysis to improve the removal of Cr(VI). The results showed that MBTS had an adsorption capacity of 54.92 mg Cr(VI)/g, which was about 14 times higher than raw burley tobacco stem biochar (i.e., 3.84 mg/g). According to the findings obtained, a three-step mechanism of Cr(VI) removal by MBTS was further put forward, i.e., (1) Cr(VI) exchanged with hydroxyl groups on MBTS, (2) the reduction in Cr(VI) to Cr(III) mediated by oxygen-containing groups, and (3) the chelation of produced Cr(III) with the amino groups on MBTS. FTIR spectra further revealed that C-N, C-H, and C=C groups played an important role in Cr(VI) removal. Furthermore, the adsorption equilibrium and kinetics of Cr(VI) on MBTS could better be described by the Langmuir equation and pseudo-second-order rate equation. This study clearly demonstrated that ferric-loaded biochar derived from burley tobacco stems could serve as a cost-effective magnetic adsorbent for the high-efficiency removal of soluble Cr(VI) from wastewater. Tobacco stem-adsorbed Cr(VI) realized a green path for treating waste by waste.

Determination of trans-fatty acids in food samples based on the precolumn fluorescence derivatization by high performance liquid chromatography.

Trans-fatty acids are unsaturated fatty acids that are considered to have health risks. 1,3,5,7-Tetramethyl-8-butyrethylenediamine-difluoroboradiaza-s-indacene is a highly sensitive fluorescent labeling reagent for carboxylic acids developed by our lab. In this study, using this precolumn fluorescent derivatization reagent, a rapid and accurate high-performance liquid chromatography with fluorescence detection method was developed for the determination of two trans-fatty acids in food samples. Under the optimized derivative conditions, two trans-fatty acids were tagged with the fluorescent labeling reagent in the presence of 1-ethyl-3-(3-dimethyl-aminopropyl) carbodiimide at 25°C for 30 min. Then, the baseline separation of trans- and cis-fatty acids and their saturated fatty acid with similar structures was achieved with less interference using a reversed-phased C18 column with isocratic elution in 14 min. With fluorescence detection at λex /λem  = 490 /510 nm, the linear range of the TFAs was 1.0-200 nM with low detection limits in the range of 0.1-0.2 nM (signal-to-noise ratio = 3). In addition, the proposed approach was successfully applied for the detection of trans-fatty acids in food samples, and the recoveries using this method ranged from 96.02 to 109.22% with low relative standard deviations of 1.2-4.3% (n = 6).

Physiological Responses and Phytotoxicities of Lythrum salicaria to Decabromodiphenyl Ether (BDE-209).

Decabromodiphenyl ether (BDE-209), a member of a major group of brominated flame retardants, is detected in aquatic environments at considerable levels and induces physiological and toxic effects on aquatic plants. In this study, the physiological responses induced by and the toxic effects of BDE-209 at different concentrations (0, 0.2, 0.5 and 1.0 mg L-1) in Lythrum salicaria were examined. OJIP transient curves indicated that BDE-209 treatment negatively affected photosystem II (PSII) grouping. Additionally, the results showed that BDE-209 inhibited seedling development and elevated reactive oxygen species (ROS), phosphorylated histone H2AX (γ-H2AX), malondialdehyde (MDA) levels and antioxidative enzyme activities in the roots and shoots of L. salicaria. The results revealed that BDE-209 exposure contributed to ROS accumulation, which was considered as the probable toxicity mechanism. The current results provided an insight into the development of L. salicaria with high BDE-209 tolerance.

Treatment performance and microbial response to dibutyl phthalate contaminated wastewater in vertical flow constructed wetland mesocosms.

Phthalic acid esters (PAEs), especially dibutyl phthalate (DBP) pollution in the environment, have attracted worldwide attention. Four Phragmites australis-based, mesocosm-scale vertical flow constructed wetlands (VFCWs) with different hydraulic loading rates (HLRs) were operated for one year to study the removal efficiency and mechanisms of DBP in the reclaimed water. The average removal efficiencies for DBP were 93.77 ± 3.27%, 94.9 ± 2.60% and 97.0 ± 3.00% in the VFCWs under HLRs of 0.33, 0.22 and 0.11 m/d, respectively. DBP can be accumulated and degraded by wetland plants and its concentration in the roots (0.256-8.45 mg/kg) were higher than in the leaves (0.243-0.482 mg/kg). The concentrations of primary and secondary metabolites mono-n-butyl phthalate (MBP) and phthalic acid (PA) were 0.142-2.35 mg/kg and 0.113-0.545 mg/kg respectively in the plant tissues. The concentrations of DBP were 38.2-271 µg/kg in the substrates. Mass balance for DBP indicates that the estimated plant uptake and substrate adsorption of total DBP is negligible. This suggests that biodegradation and other process are the primary pathways for DBP removal in VFCWs. The results of 16S rDNA and ITS rDNA high-throughput sequencing indicated that both bacterial and fungal community diversity decreased with the exposure of DBP. Janthinobacterium, Flavobacterium and Curvularia genera may be the main participants in the biodegradation of DBP in the CWs.

Removal efficiency and enzymatic mechanism of dibutyl phthalate (DBP) by constructed wetlands.

Four vertical-flow constructed wetland systems were set up in the field in order to study the removal efficiency and possible enzymatic mechanism of the constructed wetlands in treating sewage containing different concentrations of dibutyl phthalate (DBP). Under DBP spiked concentrations of 0.5, 1.0, and 2.0 mg/L, good DBP removal rates of 62.08, 82.17, and 84.17% were achieved, respectively. Meanwhile, certain removal effects of general water quality parameters were observed in all four constructed wetlands: with high average removal rates of nitrate nitrogen (NO3--N) and chemical oxygen demand (COD) of 91.10~93.89 and 82.83~89.17%, respectively, with moderate removal efficiencies of total nitrogen (TN), total phosphorus (TP), ammonia nitrogen (NH4+-N) of 44.59~49.67, 30.58~37.18, and 28.52~37.45%, respectively. Compared to the control, an increase of enzyme activities of urease, phosphatase, dehydrogenase, and nitrate reductase was observed in the treatments with DBP addition. In the presence of 0.5 mg/L of DBP concentration, the urease, phosphatase, and dehydrogenase activities reached the highest levels, with an increase of 350.02, 36.57, and 417.88% compared with the control, respectively. It appeared that the low concentration of DBP might better stimulate the release of enzymes.

Seasonal variation of microbial community for the treatment of tail water in constructed wetland.

Effects of seasons and hydraulic loading rates (HLR) on the treatment performance and the response of the microbial community of vertical flow constructed wetland treating tail water were investigated. The seasonal treatment performance was evaluated at four HLR of 125, 250, 375 and 500 mm/d, respectively. The microbial community was detected by MiSeq Illumina platform at HLR 125 and 375 mm/d. The wetland showed significantly higher chemical oxygen demand (COD) and total nitrogen (TN), total phosphorus (TP) at HLR 125 mm/d, compared with other HLR. Overall removal efficiency was 61.47%, 71.40% and 76.31% for COD, TN and TP, respectively, while no significant differences for COD, TN and TP removal were found at HLR of 250, 375 and 500 mm/d. The best removal efficiency for COD and TN was achieved in summer and autumn, while the best TP removal was achieved in winter. Nitrification bacteria (Nitrosomonas and Nitrospira) were significantly higher in HLR 125 mm/d, whereas sequences associated with denitrification had no significant difference at the two HLR. The results can partially explain the significantly higher NH4+-N removal in HLR 125 mm/d and relatively low nitrogen performance in winter.

Determination of fatty acids in bio-samples based on the pre-column fluorescence derivatization with 1,3,5,7-tetramethyl-8-butyrethylenediamine-difluoroboradiaza-s-indacene by high performance liquid chromatography.

1,3,5,7-Tetramethyl-8-butyrethylenediamine-difluoroboradiaza-s-indacene (TMBB-EDAN) has been designed and synthesized as a highly fluorescent labeling reagent for carboxylic acids. By using TMBB-EDAN, a sensitive and rapid method based on high performance liquid chromatography-fluorescence detection for the determination of twelve fatty acids (FAs) in bio-samples has been developed. Under optimized conditions, these FAs were tagged with TMBB-EDAN in the presence of 1-ethyl-3-(3-dimethyla-minopropyl) carbodiamide at 20°C for 30min and then the baseline separation was achieved on a C18 column with a linear gradient elution in 26min. With fluorescence detection at λex/λem=490nm/510nm, the linear ranges of FAs were from 3.0 to 300nM and the detection limits with a signal-to-noise ratio of 3 were in the 0.2-0.4nM range. The proposed method offers advantages of milder derivatization condition and much better sensitivity for the determination of FAs, when compared to the reported fluorescence derivatization-based methods.

[Isolation and characterization of the centromeric BAC clones from different genomes in genus Oryza].

Centromeres play an important role in ensuring the correct segregation and transmission of chromosome during mitosis and meiosis in eukaryotes. In this research, we constructed five BAC libraries for diploid wild rice with different genomes. Together with the technique of colony blot hybridization and fluorescence in situ hybridization (FISH), centromere-related BAC clones were screened and characterized from different genomes. Meanwhile, co-hybridization was detected between these clones and the five genomes. The results from this study demonstrated that: (1) there were centromere-specific satellite repeat in Oryza officinalis (CC genome) and O. brachyantha (FF genome), respectively, and centromere-specific CRR-related sequence was found in O. brachyantha; (2) homology sequences of CentO and CRR of O. sativa (AA genome) were detected on all centromeres of O. glaberrima (AA genome), O. punctata (BB genome) and O. australiensis (EE genome); And (3) the two somatic chromosomes of O. officinalis comprised of homology sequences of CentO satellites as revealed FISH analysis probed with RCS2. Homology sequences of CRR of O. sativa were also detected on all centromeres of O. officinalis. The results provided a foundation toward cloning the centromeric sequences from different genomes of genus Oryza, studying centromere organization and evolution of different genome, analyzing the relationship between centromeric structure and function among different genome.