Different effects of seasonal impoundment and land use change on microbiome in a tributary sediment of the three gorgers reservoir.

Anthropogenic activities significantly impact river ecosystem nutrient fluxes and microbial metabolism. Here, we examined the seasonal and spatial variation of sediments physicochemical parameters and the associated microbiome in the Pengxi river, a representative tributary of Three Gorges Reservoir, in response to seasonal impoundment and land use change by human activities. Results revealed that seasonal impoundment and land use change enhanced total organic carbon (TOC), total nitrogen (TN) and ammonium nitrogen (NH4+-N) concentration in the sediment, but have different effects on sediment microbiome. Sediment microbiota showed higher similarity during the seasonal high-water level (HWL) in consecutive two years. The abundant phyla Acidobacteria, Gemmatimonadetes, Cyanobacteria, Actinobacteria and Planctomycetes significantly increased as water level increased. Along the changes in bacterial taxa, we also observed changes in predicted carbon fixation functions and nitrogen-related functions, including the significantly higher levels of Calvin cycle, 4HB/3HP cycle, 3HP cycle and assimilatory nitrate reduction, while significantly lower level of denitrification. Though land use change significantly increased TOC, TN and NH4+-N concentration, its effects on spatial variation of bacterial community composition and predicted functions was not significant. The finding indicates that TGR hydrologic changes and land use change have different influences on the carbon and nitrogen fluxes and their associated microbiome in TGR sediments. A focus of future research will be on assessing on carbon and nitrogen flux balance and the associated carbon and nitrogen microbial cycling in TGR sediment.

Diversity and ecological assembly process of aerobic anoxygenic phototrophic bacteria in a low irradiation area, Three Gorges Reservoir.

Aerobic anoxygenic phototrophic bacteria (AAPB) are significant bacterial groups in aquatic ecosystems, known for their rapid growth and photoheterotrophic characteristics. However, the distribution and ecological assembly process of AAPB in low irradiation freshwater basins remain unclear, warranting further investigation. In this study, we present the diversity, abundance, spatial variations, ecological process, and community interaction of AAPB in sediment of Three Gorges Reservoir (TGR) under low irradiation. Our findings demonstrate the dominant genera of AAPB community that exist in the TGR area also are appeared in different waters, with some regional preference. Moreover, the concentration of pufM gene, an indicator for AAPB, maintains a consistently high numerical level ranging from (2.21 ± 0.44) × 104 to (9.98 ± 0.30) × 107 gene copies/g. Although solar irradiation is suggested as the major factor affecting AAPB, it remains unclear whether and how AAPB differ between regions due to varying solar irradiation levels. Our results show spatial differences between total bacteria and AAPB communities, with significant differences observed only in AAPB. Geographical and environmental factor contributed less than 10% to the spatial difference of community, with sediment type and environmental factors being the key factors influencing microbial community structure. The stochastic process plays a dominant role in the aggregation and replacement of AAPB communities, among which the most contribution is dispersal limitation. For AAPB network, Yoonia and Gemmobacter are the hubs for modules. Those results valuable insights into the AAPB communities in TGR with low irradiation.

Home-field advantage in litter decomposition: A critical review from a microbial perspective.

Litter decomposition is a key component of biogeochemical recycling. It is highly sensitive to changes in microbial community assembly. An interesting phenomenon in litter decomposition is the home-field advantage (HFA), where litter decomposes faster in native locations than in foreign sites. However, the role of the HFA in litter decomposition remains controversial. This review examines current evidence relating to the HFA using the leaf economics spectrum theory and the Lotka-Volterra niche competition model and explains its influence on the microbial assembly process. Here, it is proposed that the microbial community assembly could help to explain the HFA at spatiotemporal scales. This review improves understanding of the role of the succession of microbial communities in HFA litter decomposition and in the elemental cycle of forest systems.

Enhancing sensitivity of microbial fuel cell sensors for low concentration biodegradable organic matter detection: Regulation of substrate concentration, anode area and external resistance.

The relatively low sensitivity is an important reason for restricting the microbial fuel cell (MFC) sensors' application in low concentration biodegradable organic matter (BOM) detection. The startup parameters, including substrate concentration, anode area and external resistance, were regulated to enhance the sensitivity of MFC sensors. The results demonstrated that both the substrate concentration and anode area were positively correlated with the sensitivity of MFC sensors, and an external resistance of 210 Ω was found to be optimal in terms of sensitivity of MFC sensors. Optimized MFC sensors had lower detection limit (1 mg/L) and higher sensitivity (Slope value of the linear regression curve was 1.02), which effectively overcome the limitation of low concentration BOM detection. The essential reason is that optimized MFC sensors had higher coulombic efficiency, which was beneficial to improve the sensitivity of MFC sensors. The main impact of the substrate concentration and anode area was to regulate the proportion between electrogens and nonelectrogens, biomass and living cells of the anode biofilm. The external resistance mainly affected the morphology structure and the proportion of living cells of the anode. This study demonstrated an effective way to improve the sensitivity of MFC sensors for low concentration BOM detection.

Evaluation of simultaneous autotrophic and heterotrophic denitrification processes and bacterial community structure analysis.

This study demonstrated that a combined heterotrophic and autotrophic denitrification (HAD) process is highly effective for the simultaneous removal of acetate, nitrate, and sulfide at an efficiency of 100, 80, and 100 %, respectively. In the HAD system, simultaneous sulfide, acetate, and nitrate removals were observed, which indicated that heterotrophic and autotrophic denitrification occurred simultaneously. When the sulfide was existed in HAD reactor, the main product of sulfide biooxidation was S(0). Once the sulfide was exhausted, the sulfate concentration in the HAD reactor increased and became the main end product. These results provided an alternative method to control the end sulfide biooxidation product by online monitoring sulfide concentration. Nearly half (43 %) of the total clones in our mix-trophic reactor were amphitrophy denitrifiers. The autotrophic denitrifiers, heterotrophic denitrifiers, and amphitrophy denitrifiers coexisted in the HAD reactor to complete the denitrification process. Retrieved bacterial 16S rRNA gene clones affiliated with uncultured Xanthomonadaceae, Thauera, Thiobacillus, and Chromatiales were dominant.

The heterotrophic-combined-with-autotrophic denitrification process: performance and interaction mechanisms.

In this work, the interaction mechanisms between an autotrophic denitrification (AD) and heterotrophic denitrification (HD) process in a heterotrophic-autotrophic denitrification (HAD) system were investigated, and the performance of the HAD system under different S/Ac(-) molar ratios was also evaluated. The results demonstrated that the heterotrophic-combined-with-autotrophic denitrification process is a promising technology which can remove chemical oxygen demand (COD), sulfide and nitrate simultaneously. The reduction rate of NO(3)(-) to NO(2)(-) by the HD process was much faster than that of reducing NO(2)(-) to N2, while the reduction rate of NO(3)(-) to NO(2)(-) by the AD process was slower than that of NO(2)(-) to N2. Therefore, the AD process could use the surplus NO(2)(-) produced by the HD process. This could alleviate the NO(2)(-)-N accumulation and increase the denitrification rate. In addition, the inhibition effects of acetate on AD bacteria and sulfide on HD were observed, and the inhibition was compensated by the promotion effects on NO(2)(-). Therefore, the processes of AD and HD seem to react in parallel, without disturbing each other, in our HAD system.

Estimation of PM10 in the traffic-related atmosphere for three road types in Beijing and Guangzhou, China.

The levels of roadside PM10 in Beijing, China, were investigated in 2011 and 2012 on a seasonal basis to estimate the population exposure to particulates for three road types. The measurements of PM10 were also conducted in the southern Chinese megacity of Guangzhou for comparison purposes. The results showed that roadside PM10 in Beijing correlated strongly with the PM10 background in the urban atmosphere. The levels of PM10 in street canyons were markedly higher than those along the open roads and in crossroad areas because of limited ventilation. An elevation of PM10 was observed in April, which was possibly due to the sand storms that frequently occur in the spring. Based on these observations, roadside PM10 in Beijing could have multiple origins and was to some extent dispersion-governed. In Guangzhou, the roadside PM10 did not closely relate to the background values. The PM10 pollution was greatly affected by local traffic conditions. The simulation of PM10 for different road types was completed during the study period using the Motor Vehicle Emissions Factor Model (MOBILE6.2) as an emission model and the California Line Source Dispersion Model (CALINE4) and Operational Street Pollution Model (OSPM) as dispersion models. The MOBILE6.2/CALINE4 software package was demonstrated to be sufficient for the simulation of PM10 in the open roads and crossroad areas in both Beijing and Guangzhou, and the simulation results of roadside PM10 in the street canyons by the MOBILE6.2/OSPM package were in close agreement with those of the measurements.

Anaerobic ammonium oxidation coupled to Fe(III) reduction: Discovery, mechanism and application prospects in wastewater treatment.

Fe(III) reduction coupled with anaerobic ammonium oxidation is known as Feammox. Feammox, which was first discovered in wetland ecosystems, has the potential to be used in wastewater treatment systems due to its ability to remove ammonium. Feammox can produce N2, NO2- or NO3- through the reduction of Fe(III) and oxidation of ammonium, which is a potential process to nitrogen loss from aquatic ecosystems and terrestrial ecosystems. The Acidimicrobiaceae sp. A6 was the first Feammox functional bacteria that was successfully isolated from wetlands. The nitrogen removal effect of Feammox can be influenced by many environmental factors, such as pH, organic matter, and different sources of Fe(III). Feammox has broad application prospects, but more exploration is needed to apply this principle to wastewater treatment. This review introduces the development, mechanism, functional microbes and factors affecting the Feammox process, and discusses its potential applications.

[Effect of Chelated Iron on Nitrogen Removal Efficiency and Microbial Community Structure in the Anaerobic Ferric Ammonium Oxidation].

In order to understand the characteristics and interactions of the microbial community during the anaerobic ferric ammonium oxidation (FEAMMOX) process, this study investigated the effects of various forms of chelated iron on nitrogen removal efficiency and microbial community structure. After 77 days of reactor operation, the removal efficiency of total nitrogen was 83.32% for the ferric humate group, 43.67% for the ferric citrate group, 55.07% for the ferric sodium ethylene diamine tetraacetate group, and 12.65% for the ferric ammonium triacetate group. After the experiment, the abundance of denitrifying bacteria Comamonadaceae in ferric humate group was 17.57%, the abundance of Clostridium in ferric citrate group was 47.70%; and the abundance of denitrifying bacteria Thermomonas in the ferric sodium ethylene diamine tetraacetate group was 20.11%. This indicates that ferric humate is a more effective electron acceptor for the FEAMMOX process. The result of function prediction shows that the iron, sulfur, and nitrogen cycles are all closely related, with iron and sulfur metabolism playing an important role in nitrogen removal. In the humate group, iron respiration and the nitrogen cycle are more strongly correlated than other groups. Co-occurrence network analysis showed that the keystone species in the FEAMMOX process is Tessaracoccus.

Characterizing the removal routes of seven pharmaceuticals in the activated sludge process.

The removal routes of pharmaceuticals especially biodegradation routes in the activated sludge process are still unclear. Some studies indicated pharmaceuticals were mainly removed via nitrification process (autotrophic biodegradation), while others suggested pharmaceuticals were mainly removed via COD degradation process (heterotrophic biodegradation). These unclear problems limited the improvements of pharmaceuticals removal. In this study, in order to elucidate three biodegradation routes (nitrification, COD degradation, or both nitrification and COD degradation), autotrophic and heterotrophic reactors were individually developed to separate nitrification and COD degradation form the activated sludge process (mix-trophic process including nitrification and COD degradation). Furthermore, the pharmaceuticals removal routes of adsorption, hydrolysis, and oxidation were also studied. Among six degradable pharmaceuticals, heterotrophic biodegradation and adsorption were the major removal routes. Two sulfonamides of five antibiotics were predominantly removed by COD degradation process, while nitrification and adsorption had no contributions. Adsorption, hydrolysis, nitrification, and COD degradation were the main elimination routes of cefalexin. COD degradation and adsorption were the dominant removal routes of norfloxacin. Tetracycline was mainly removed by the adsorption route, and hydrolysis and oxidation also played a role. For two drugs, ibuprofen was removed mainly via nitrification and COD degradation, and no adsorption occurred. Diclofenac could not be removed at all and was persistent in the aerobic conditions. Kinetic studies showed that biodegradation of the two sulfonamides, cefalexin, norfloxacin, and ibuprofen followed first-order kinetics rather than zero-order or second-order kinetics.

Autocatalysis in Reactive Black 5 biodecolorization by Rhodopseudomonas palustris W1.

Autocatalysis in biological decolorization of Reactive Black 5 (RB5) by Rhodopseudomonas palustris W1 was investigated in batch assays. An improvement of 1.5-fold in decolorization rate of RB5 was obtained by supplementing decolorization metabolites from 200 mg l(-1) RB5. Liquid chromatography-mass spectrometry and cyclic voltammetric analysis revealed that the constituent of dye precursors, from azo bonds breakage, with quinone-like structure and reversible oxidation-reduction activity can be used as redox mediators and was responsible for the catalytic reduction of RB5. The required amount of metabolites for catalytic decolorization was quite small, indicating its possible application in real textile wastewater treatment. Furthermore, decolorization metabolites of RB5 were shown as effective in catalyzing anaerobic decolorization of Direct Yellow 11, an azo dye without autocatalyic activity.

Biodecolorization and partial mineralization of Reactive Black 5 by a strain of Rhodopseudomonas palustris.

A strain of photosynthetic bacterium, Rhodopseudomonas palustris W1, isolated from a lab-scale anaerobic moving bed biofilm reactor (MBBR) treating textile effluent was demonstrated to decolorize Reactive Black 5 (RB5) efficiently under anaerobic condition. By a series of batch tests, the suitable conditions for RB5 decolorization were obtained, namely, pH < 10, light presence, glutamine or lactate as carbon source with concentration more than 500 mg/L when lactate is selected, NH4Cl as a nitrogen source with concentration more than 100 mg/L, NaCl concentration not exceeding 5%, and RB5 concentration less than 700 mg/L. In addition, ultraviolet-visible (UV-Vis) spectrum scan and High Performance Liquid Chromatography/Mass Spectrometry (HPLC-MS) were used to analyze the metabolites of RB5 decolorization of W1. The results showed that partial aromatic amines produced with RB5 reduction were further degraded during the extended period. Anaerobic partial mineralization of RB5 was suggested, and a possible degradation pathway was proposed.

New insights in photosynthetic microbial fuel cell using anoxygenic phototrophic bacteria.

Anoxygenic phototrophic bacteria (APB) pay a key role in biogeochemical cycles, and it can convert light energy to chemical energy by photosynthesis process. Photosynthetic microbial fuel cell (photo-MFC) is regarded as a promising energy-harvesting technology, which is also applied to environment treatment in recent years. The previous studies show that photo-MFC with APB have higher power putout than other bioelectrochemical systems. However, photo-MFC with APB is not reviewed due to some limited factors in the development process. In this review, photo-MFC with APB is treated according to its electron transfer pathways, the current understanding, APB strains, application, influence of substrates, and economic assessment. Meanwhile, knowledge of photosynthesis components and electron transfer pathways of APB is crucial for developing new energy and easing the serious energy crisis. Moreover, some new insights (the optimization of light source and self-sustaining bioelectricity generation) are proposed for the future explorations.

The exploration of monochromatic near-infrared LED improved anoxygenic photosynthetic bacteria Rhodopseudomonas sp. for wastewater treatment.

The future wastewater treatment requires high-efficiency and energy-saving technology. Anoxygenic photosynthetic bacteria (APB) is deemed as an eco-friendly microorganism, which could be employed in wastewater treatment. Here, monochromatic near-infrared (MNIR) light emitting diode (LED) was used, and three key factors (light quality, light intensity and photoperiod) of it were analyzed by a response surface methodology (RSM) in APB wastewater treatment. The results showed that light quality was the biggest impact factor in APB wastewater treatment, and nearly 58.07% of NH4+-N and 70.62% of chemical oxygen demand (COD) could be removed based on 46.4% of that theoretically possible. The light quality's study revealed that APB had the highest NH4+-N and COD removal, biomass production, and bacteriochlorophyll a production with 850nm IR LED. Moreover, the application of optimal MNIR LED could not only save energy, but also avoid algae bloom of photo-bioreactors (PBR).

Calcium precipitate induced aerobic granulation.

Aerobic granulation is a novel biotechnology for wastewater treatment. This study refined existing aerobic granulation mechanisms as a sequencing process including formation of calcium precipitate under alkaline pH to form inorganic cores, followed by bacterial attachment and growth on these cores to form the exopolysaccharide matrix. Mature granules comprised an inner core and a matrix layer and a rim layer with enriched microbial strains. The inorganic core was a mix of different crystals of calcium and phosphates. Functional strains including Sphingomonas sp., Paracoccus sp. Sinorhizobium americanum strain and Flavobacterium sp. attached onto the cores. These functional strains promote c-di-GMP production and the expression by Psl and Alg genes for exopolysaccharide production to enhance formation of mature granules.

Fate and transformation of naphthylaminesulfonic azo dye reactive black 5 during wastewater treatment process.

Certain aromatic amines generated by the decolorization of some azo dyes are not removed substantially by conventional anaerobic-aerobic biotreatment. These aromatic amines are potentially toxic and often released in the wastewater of industrial plants. In this study, the fate and transformation of the naphthylaminesulfonic azo dye Reactive Black 5 (RB5) during different phases of a sequencing batch reactor were investigated. The major products of RB5 decolorization during the anaerobic phase include 2-[(4-aminophenyl)sulfonyl]ethyl hydrogen sulfate (APSEHS) and 1-2-7-triamino-8-hydroxy-3-6-naphthalinedisulfate (TAHNDS). During the aerobic phase, APSEHS was hydrolyzed and produced 4-aminobenzenesulfonic acid, which was further degraded via dearomatization. TAHNDS was transformed rapidly via auto-oxidation into TAHNDSDP-1 and TAHNDSDP-2, which were not further removed by the activated sludge during the entire 30-day aerobic phase. In contrast, different behaviors of TAHNDS were observed during the anoxic phase. The transformation of TAHNDS was initiated either by deamination or desulfonation reaction. TAHNDS was then converted into 3,5-diamino-4-hydroxynaphthalene-2-sulfonic acid, which was subsequently removed via ring cleavage reaction under aerobic condition. In conclusion, complete degradation of TAHNDS by activated sludge occurs only during anoxic/aerobic processes instead of the conventional anaerobic/aerobic processes.

TiO2/bi A-SPAES(Ds 1.0) composite membranes for proton exchange membrane in direct methanol fuel cell (DMFC).

A series of TiO2/bi A-SPAES(Ds 1.0) composite membranes with various contents of nano-sized TiO2 particles were prepared through sol-gel method. Scanning electron microscopy (SEM) images indicated the TiO2 particles were well dispersed within polymer matrix. These membranes were used for proton exchange membrane (PEM) for performance evaluation in direct methanol fuel cell (DMFC). These composite membranes showed good thermal stability and mechanical strength. It was found that the water uptake of these membranes enhanced with the TiO2 amount increasing in these composite membranes. Meanwhile, the introduction of TiO2 particles increased the proton conductivity and reduced the methanol permeability. The proton conductivities of these composite membranes with 8% TiO2 particles (0.120 S/cm and 0.128 S/cm) were higher than those of Nafion 117 membrane (0.114 S/cm and 0.117 S/cm) at 80 degrees C and 100 degrees C. Specially, the methanol diffusion coefficient (1.2 x 10(-7) cm2/s) of the composite membrane with 8% TiO2 content was much lower than that of Nafion 117 membrane (2.1 x 10(-6) cm2/s). As a result, the TiO2/bi A-SPAES composite membrane was considered as a promising material for PEM in DMFC.

Influence of calcination on the adsorptive removal of phosphate by Zn-Al layered double hydroxides from excess sludge liquor.

The influence of calcination of Zn-Al layered double hydroxides (LDHs) on their phosphate adsorption capacity was studied in order to improve phosphorus removal from an excess sludge liquor. Powder X-ray diffraction (XRD), Fourier transform infrared (FTIR) spectroscopy, scanning electron microscopy (SEM), thermogravimetry-differential scanning calorimetry (TG-DSC) and nitrogen adsorption-desorption were employed to characterize the raw Zn-Al and the calcined products. The results reveal that the Zn-Al LDHs evolved to a phase of mixed metal oxides with the calcination temperature increasing to 300 degrees C and finally to spinel ZnAl(2)O(4) at 600 degrees C. When the Zn-Al was calcined at 300 degrees C, the interlayer carbonate ions were removed and the greatest BET surface area of 81.20 m(2)/g was achieved. The tested phosphate adsorption capacities of the raw and calcined Zn-Al were closely related to the evolution of physicochemical properties of the LDHs during the calcination. The Zn-Al-300 (Zn-Al LDHs calcined at 300 degrees C) exhibited the highest P uptake of 41.26 mg P/g in 24h. The phosphate adsorption by the raw Zn-Al and the Zn-Al-300 both follows a pseudo-second-order kinetic model; the adsorption isotherms show a good fit with a Langmuir-type equation.

Phosphate adsorption from sewage sludge filtrate using zinc-aluminum layered double hydroxides.

A series of layered double hydroxides (LDHs) with different metal cations were synthesized to remove phosphate in waste sludge filtrate from a municipal wastewater treatment plant for phosphorus recovery and to help control eutrophication. The highest phosphate adsorption capacity was obtained by using Zn-Al-2-300, that is LDHs with Zn/Al molar ratio of 2 and calcined at 300 degrees C for 4h. Circumneutral and mildly alkaline waters appeared suitable for the possible application of Zn-Al LDHs due to the amphoteric nature of aluminum hydroxide. Phosphate adsorption from the sludge filtrate by the LDHs followed pseudo-second-order kinetics, and the adsorption capacity at equilibrium was determined to be approximately 50 mg P/g. Adsorption isotherms showed that phosphate uptake in this study was an endothermic process and had a good fit with a Langmuir-type model. The absorbed phosphate can be effectively desorbed (more than 80%) from LDHs particles by a 5 wt% NaOH solution. The regeneration rate of used LDHs was approximately 60% after six cycles of adsorption-desorption-regeneration.