The diversity of planktonic bacteria driven by environmental factors in different mariculture areas in the East China Sea.

Planktonic bacteria play a crucial role in sustaining the ecological balance of aquatic ecosystems. However, their seasonal variations in different aquaculture areas within the East China Sea, along with their correlation to environmental factors, have not been extensively explored. In this study, each area with 3 sample points were set up to represent the fish aquaculture area, shellfish aquaculture area and non-aquaculture area. In 2019, we undertook four marine surveys along the Xiasanhengshan uninhabited island, during which we gathered surface seawater samples for both physicochemical analysis and high-throughput sequencing. This allowed us to obtain data about the physicochemical properties and microbial composition in each surveyed region. A short-term eutrophication phenomenon was present in the sea, and the spatial and temporal distribution of planktonic bacteria differed based on the mariculture area. At the phylum level, Proteobacteria accounted for >50 % of the community abundance in winter, spring, and autumn, while Cyanobacteria accounted for >30 % of the community abundance in summer. Because Cyanobacteria blooms are likely in summer, the relationship between Cyanobacteria and environmental factors was studied. Redundancy analysis showed that Cyanobacteria were consistently positively correlated with phosphate. Eutrophication and abnormal proliferation of Cyanobacteria in the study area necessitate ameliorations in the mariculture structure. The variation of genus in Proteobacteria is consistent with that of eutrophication, so some genera in Proteobacteria have the potential to become biological indicator species.

Effects of running time on biological activated carbon filters: water purification performance and microbial community evolution.

Ozone-biologically activated carbon (BAC) filtration is an advanced treatment process that can be applied to remove recalcitrant organic micro-pollutants in drinking water treatment plants (DWTPs). In this study, we continuously monitored a new and an old BAC filter in a DWTP for 1 year to compare their water purification performance and microbial community evolution. The results revealed that, compared with the new filter, the use of the old BAC filter facilitated a slightly lower rate of dissolved organic carbon (DOC) removal. In the case of the new BAC filter, we recorded general increases in the biomass and microbial diversity of the biofilm with a prolongation of operating time, with the biomass stabilizing after 7 months. For both new and old BAC filters, Proteobacteria and Acidobacteria were the dominant bacterial phyla. At the genus level, the microbial community gradually shifted over the course of operation from a predominance of Herminiimonas and Hydrogenophaga to one predominated by Bradyrhizbium, Bryobacter, Hyphomicrobium, and Pedomicrobium, with Bradyrhizobium being established as the most abundant genus in the old BAC filter. Regarding spatial distribution, we detected reductions in the biomass and number of operational taxonomic units with increasing biofilm depth, whereas there was a corresponding increase in microbial diversity. However, compared with the effects of time, the influence of depth on the composition of the biofilm microbial community was considerably smaller. Furthermore, co-occurrence network analysis revealed that the microbial community network of the new filter after 11 months of operation was the most tightly connected, although its modular coefficient was the lowest of those assessed. We speculate that the positive and negative interactions within the network may be attributable to symbiotic or competitive relationships among species. Moreover, there may have been a significant negative interaction between SWB02 and Acidovorax, plausibly associated with a competition for substrates.

Invasion mechanism of Spartina alterniflora by regulating soil sulfur and iron cycling and microbial composition in the Jiuduansha Wetland.

Spartina alterniflora, an invasive plant widely distributed in China's coastal regions, has had a significant impact on the stability of wetland ecosystems and elemental biogeochemical cycles. The invasion of S. alterniflora has been found to lead to the accumulation of sulfides in the soil. The cycling of sulfur and iron in the soil is closely interconnected. Coastal estuarine wetlands are influenced by both freshwater in rivers and seawater tides, as well as the frequent variations in redox conditions caused by tidal fluctuations, which makes the cycling of sulfur and iron in the soil invaded by S. alterniflora more intricate. In this study, field surveys and laboratory experiments were conducted to explore the effects of S. alterniflora invasion and hydrological changes on the cycling of sulfur and iron as well as related functional microorganisms in the soil. The invasion of S. alterniflora showed an increase in soil reduced inorganic sulfur (RIS) components in both high and low marshes of Jiuduansha wetland, with higher content observed in summer and autumn. The tidal simulation experiments revealed abundant sulfate in seawater tidal conditions could promote the formation of acid volatile sulfides (AVS) in the soil of low marshes invaded by S. alterniflora and ensuring the continuous increase in AVS content. Diffusive gradients in-thin-films (DGT) technology indicated the existence of high-concentration soluble S2- enrichment zones in the soil of low marshes invaded by S. alterniflora, which may be related to S. alterniflora root exudates. Tidal action increased the relative abundance of sulfur-reducing bacteria (SRB) in the soil of low marshes, and under the influence of seawater tidal action, SRB exhibited higher relative abundance. However, S. alterniflora might inhibit the activity of iron-reducing bacteria (FeRB) in the soil of low marshes. In conclusion, S. alterniflora may enhance the sulfate reduction rate and promote the formation of free sulfides in tidal salt marsh ecosystems by releasing root exudates that stimulate the activity of SRB, while concurrently inhibiting the activity of FeRB and reducing their competition with SRB. This effect is particularly pronounced in low marshes under seawater tidal conditions. Thus, S. alterniflora is capable of rapidly invading tidal salt marshes by utilizing sulfides effectively.

Effect of aging on the release of di-(2-ethylhexyl) phthalate from biodegradable and petroleum-based microplastics into soil.

Due to microplastics (MPs) being widely distributed in soil, the use of advanced oxidation to remediate organic-contaminated soils may accelerate the aging of MPs in soil and impact the release of di-(2-ethylhexyl) phthalate (DEHP), a potential carcinogen used as a plasticizer in plastics, from MPs. In this study, persulfate oxidation (PO) and temperature treatment (TT) were used to treat biodegradable and petroleum-based MPs, including polylactic acid (PLA), polyvinyl chloride (PVC), and polystyrene (PS). The methods used for evaluating the characteristics changes of MP were X-ray diffraction (XRD) analysis and water contact angle measurement. The effects of aging on DEHP release from MPs were investigated via soil incubation. The results showed PO and TT led to increased surface roughness, oxygen-containing functional group content, and hydrophilicity of the MPs with prolonged aging, consequently accelerating the release of DEHP from the MPs. Interestingly, PLA aged faster than PVC and PS under similar conditions. After 30 days of PO treatment, DEHP release from PLA into the soil increased 0.789-fold, exceeding the increase from PVC (0.454-fold) and PS (0.287-fold). This suggests that aged PLA poses a higher ecological risk than aged PVC or PS. Furthermore, PO treatment resulted in the oxidation and degradation of DEHP on the MP surface. After 30 days of PO treatment, the DEHP content in PLA, PVC, and PS decreased by 19.1%, 25.8%, and 23.5%, respectively. Specifying the types of MPs studied and the environmental conditions would provide a more precise context for the results. These findings provide novel insights into the fate of biodegradable and petroleum-based MPs and the potential ecotoxicity arising from advanced oxidation remediation in contaminated soils.

Effect of particle size and environmental conditions on the release of di(2-ethylhexyl) phthalate from microplastics.

The extensive use and improper handling of plastics have caused extensive microplastic (MP) pollution in terrestrial environments. Di(2-ethylhexyl) phthalate (DEHP), the main additive used in plastics, is toxic to organisms and may pose risks to human and animal reproductive functions. However, research on the release behavior of DEHP from MPs is scarce. In this study, the effects of particle size and environmental conditions (temperature, pH, ionic strength, and cation type) on DEHP release from polylactide (PLA), polystyrene (PS), and polyvinyl chloride (PVC) MPs were determined by performing leaching experiments. The results showed that when particle size decreased, the content of DEHP in the MPs and the amount of released DEHP increased though increasing specific surface area. An increase in temperature also promoted DEHP release; when the temperature increased from 15 °C to 45 °C, the amount of DEHP released from PLA, PS, and PVC increased by 38.4%, 71.0%, and 109%, respectively. The lower the crystallinity, the greater the increase in the amount of DEHP released. Ionic strength inhibited the release of DEHP from MPs. When Na+ concentration increased from 0 to 200 mM, the amount of DEHP released from PLA, PS, and PVC decreased by 27.4%, 41.6%, and 35.3%, respectively. The effect of Ca2+ on DEHP release from MPs was greater than that of Na+. In addition, the process of DEHP release from MPs fit well with a pseudo-first-order kinetic model. The results of this study provide a theoretical basis for managing and controlling the risks associated with plastic wastes.

Spatiotemporal variations and dominated environmental parameters of nitrous oxide (N2O) concentrations from cascade reservoirs in southwest China.

Anthropogenic activity has caused rivers and reservoirs to become sources of nitrous oxide (N2O), which is thought to play an important role in global climate change. There are thermal and DO stratification in deep-water reservoirs with long hydraulic retention time, which change N2O production mechanism compared with shallow-water reservoirs. To promote our understanding of the relationship of N2O production in reservoirs at different depths, spatiotemporal variations in water environmental factors and N2O from cascade reservoirs of Chaishitan (CST), Longtan (LT), Yantan (YT) and Dahua (DH) reservoirs in the Zhujiang River were detected, and the LT and YT reservoirs were compared as representatives of deep-water and shallow-water reservoirs in April and July 2019. The average N2O concentrations in the LT and YT reservoirs were 22.82 ± 2.21 and 21.55 ± 1.65 nmol L-1, respectively. During spring and summer, the WT (water temperature) and DO (dissolved oxygen) concentrations in the YT reservoir were well mixed. In contrast, the LT reservoir, as a deep-water reservoir, had thermal and DO stratifications in both the shallow and middle water, especially in the summer when the solar radiation intensity was high. During summer stratification, the DO concentration in the LT reservoir showed obvious spatial variation, ranging from 1.23 to 9.84 mg L-1, while the DO concentration in the YT reservoir showed very little variation, ranging from 6.45 to 7.09 mg L-1. Structural equation modeling results showed that NH4+ was the main determinant of the N2O concentration in the YT reservoir, and DO was the most influential factor of the N2O concentration in the LT reservoir. These results suggest significant variations in the factors influencing N2O concentration among reservoirs. Additionally, the mechanisms of N2O production differ between deep-water and shallow-water reservoirs. This study highlights the spatio-temporal variations and influential factors contributing to N2O concentration. Furthermore, it discusses the production mechanisms of N2O in different types of reservoirs. These findings contribute to our understanding of N2O distribution in hydropower systems and provide valuable data for the management of hydropower facilities and research on greenhouse gas emissions.

Effects of phosphate addition on the removal of disinfection by-product formation potentials by biological activated carbon filtration.

In drinking water treatment plants (DWTPs), the widely used biological activated carbon filters (BACFs), as the last barrier before disinfection, can remove dissolved organic matter (DOM) known as precursors of disinfection by-products (DBPs). Whether phosphate addition can improve water purification and DBP control of BACFs is still controversial. This study investigated short-term and long-term effects of phosphate addition on controlling DBP formation potentials (FPs) by BACFs via column and batch experiments. The BAC columns presented good water purification performance: they removed around 50 % DOM, nearly all fulvic acid-likes and humic acid-likes as well as 5 %-70 % chlor(am)innated THM4, HAA9 and HAN4 FPs (except chloraminated THM4 FPs)， which was mainly contributed by aerobic bacteria not anoxic bacteria. Phosphate addition within 7-14 days further improved removals of DOM, aromatic organics, fluorescence fractions in DOM as well as HAA9 and HAN4 FPs (especially TCAA FP and TCAN FP) to different extent. However, this improvement did not last longer, and removals of DOM, aromatic organics, two fluorescence fractions (soluble microbial byproduct-likes and humic acid-likes) and DBP FPs decreased despite long-term phosphate addition. Oxic and anoxic batch experiments showed that the positive response of water purification to short-term phosphate addition was also mainly attributed to aerobic bacteria and not to anoxic bacteria. For example, the former decreased DOM and DBP FPs, while the latter increased protein- and tryptophan-like substances as well as chloraminated THM4 FPs. Phosphate addition resulted in EPS increase in anoxic reactors and decrease in oxic reactors. These results indicated that a high dissolved oxygen in BACFs may be helpful for water purification and DBP control. Overall, short-term phosphate addition into phosphorus-limited water is beneficial for BACFs to control DBPs while long-term addition has no effect. Therefore, an intermittent phosphate addition into BACFs is suggested to control DBPs in DWTPs.

Lurgi-Thyssen dust catalytic thermal desorption remediation of di-(2-ethylhexyl) phthalate contaminated soils.

Fe2O3-assisted pyrolysis has been demonstrated to be a cost-effective thermal desorption (TD) technology. Lurgi-Thyssen dust (LTD) is a type of steel slag waste that contains a large amount of Fe2O3. In this study, to reduce energy consumption, LTD was added to contaminated soil to evaluate the feasibility of enhancing the TD removal efficiency of di-(2-ethylhexyl) phthalate (DEHP). The DEHP removal rate increased by 22.39% after adding 2% LTD at 200 °C for 20 min. Because of the catalytic pyrolysis of LTD, DEHP was pyrolyzed to form three types of short-chain esters: mono-(2-ethylhexyl) phthalate (MEHP), di (2-methylbutyl) ester, and methyl 2-ethylhexyl phthalate. The pyrolysis products of DEHP were less toxic and did not affect soil reuse. When the DEHP removal rate was 87.10%, LTD addition decreased the temperature and residence time of TD and alleviated the effect of TD on the soil physicochemical properties. Additionally, the desorption of DEHP from soil fitted the pseudo-second-order kinetic model well. Thus, the addition of LTD to contaminated soil enhanced the efficiency of TD remediation. Moreover, this study could provide a practical and economical strategy for LTD reuse.

Submerged macrophytes regulate diurnal nitrous oxide emissions from a shallow eutrophic lake: A case study of Lake Wuliangsuhai in the temperate arid region of China.

Submerged macrophytes can increase oxygen concentrations of water and promote diel oxygen fluctuations, and this phenomenon is hypothesized to play a vital role in regulating nitrous oxide (N2O) emissions from eutrophic lakes. However, the effects of submerged macrophytes on N2O emissions in shallow eutrophic lakes remain poorly investigated. In this study, Lake Wuliangsuhai, a typical shallow eutrophic lake, was investigated to study the role of submerged macrophytes in regulating N2O emissions. We measured the N2O fluxes and related parameters through continual 72-h in situ diel monitoring in two sampling sections that covered dense submerged macrophyte areas and open water. In this study, the dissolved oxygen (DO) concentration of the water in the submerged macrophyte area exhibited significant diurnal variations, with significantly higher water oxygen concentrations than the open water area during the daytime. The N2O fluxes of Lake Wuliangsuhai ranged from 0.01 to 0.24 µmol m-2 h-1, with an average value of 0.11 µmol m-2 h-1. Moreover, significant diel variations in the N2O flux and net N2O production were observed in the submerged macrophyte areas, where the maximum N2O flux occurred at midday. The molar ratios of NH4+-N to oxygen (N/O ratio) of the water were responsible for the diel variations in the N2O production in the lake. However, the high oxygen concentration of the water was the major regulator of the N2O flux of Lake Wuliangsuhai. Therefore, submerged macrophyte restoration is significant not only for water quality improvement in shallow eutrophic lakes but also for N2O emission mitigation by increasing the DO concentration of the water.

Efficient degradation of Congo red and phenol by a new photocatalyst Ag/AgBr-Al-attapulgite composite under visible light irradiation.

Nowadays the concern on the treatment of refractory organic pollutants (e.g., Congo red and phenolic compounds) in industrial wastewaters and their treated effluents with conventional technologies has been still continuously increasing. In this study, a novel visible light photocatalyst material, Ag/AgBr and Al loading on the attapulgite (ATP), was prepared for efficiently catalyzing the photodegradation of the two refractory substances, and its photocatalytic performance and recyclability were assessed. Results from transmission electron microscopy and X-ray diffraction confirmed the successful loading of Ag/AgBr and Al on the ATP. The prepared Ag/AgBr-Al-ATP composite presented substantially better catalytic performance than Ag/AgBr alone probably because the ATP as a carrier of catalyst provided more contact surface for catalyst Ag/AgBr and Congo red/phenol. In the Ag/AgBr-Al-ATP composite, the photocatalyst AgBr content increased from 20.4 to 34.9% due to the modification of ATP by Al. Correspondingly, the Ag/AgBr-Al-ATP composite presented its excellent photocatalytic performance under visible light irradiation: photodegradation efficiencies of Congo red and phenol of 1.73 mg/100 mg and 0.86 mg/100 mg were achieved. With the increase of pH, the photolysis efficiencies of Congo red and phenol both first increased and then decreased, whereas the optimal photocatalytic performance occurred at pH 7 for Congo red and pH 10 for phenol. The Ag/AgBr-Al composite presented a high catalytic activity for photolysis of Congo red and phenol in all the four consecutive reused cycles. The results in this study comprehensively demonstrated a promising photocatalyst for efficient removal of the similar refractory organics presented in industrial wastewaters, which deserves further investigation and development.

Filamentous green algae Spirogyra regulates methane emissions from eutrophic rivers.

Excessive growth of filamentous green algae in rivers has attracted much attention due to their functional importance to primary production and carbon cycling. However, comprehensive knowledge of how filamentous green algae affect carbon cycling, especially the CH4 emissions from river ecosystems, remains limited. In this study, incubation experiments were conducted to examine the factors regulating CH4 emissions from a eutrophic river with dense growth of filamentous green algae Spirogyra through combinations of biogeochemical, molecular biological, and stable carbon isotope analyses. Results showed that although water dissolved oxygen (DO) in the algae+sediment (A+S) incubation groups increased up to 19 mg L-1, average CH4 flux of the groups was 13.09 µmol m-2 day-1, nearly up to two times higher than that from sediments without algae (S groups). The significant increase of sediment CH4 oxidation potential and methanotroph abundances identified the enhancing sediment CH4 oxidation during Spirogyra bloom. However, the increased water CH4 concentration was consistent with depleted water [Formula: see text] and decreased apparent fractionation factor (αapp), suggesting the important contribution of Spirogyra to the oxic water CH4 production. It can thus be concluded that high DO concentration during the algal bloom promoted the CH4 consumption by enhancing sediment CH4 oxidation, while algal-linked oxic water CH4 production as a major component of water CH4 promoted the CH4 emissions from the river. Our study highlights the regulation of Spirogyra in aquatic CH4 fluxes and will help to estimate accurately CH4 emissions from eutrophic rivers with dense blooms of filamentous green algae. Graphical abstract.

Magnetic Fe3O4@CoFe-LDH nanocomposite heterogeneously activated peroxymonosulfate for degradation of azo-dye AO7.

In this study, a novel core@shell magnetic nanocomposite Fe3O4/CoFe-layered double hydroxide (Fe3O4@CoFe-LDH) was successfully synthesized by the co-precipitation method, and then employed as an efficient heterogeneous catalyst for activation of peroxymonosulfate (PMS) in removal of azo-dye acid orange 7 (AO7). The as-obtained nanocomposite was characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), scanning electron microscopy (SEM) and vibrating sample magnetometer (VSM). The results from these characterizations showed Fe3O4@CoFe-LDH to possess good ferromagnetism and a perfect crystalline structure with a typical core@shell morphology. The system of Fe3O4@CoFe-LDH11/PMS (cobalt : iron molar ratio of 1 : 1) achieved 95.1% removal rate of AO7 (40 mg L-1) within 15 min under the optimized conditions, which outperformed bare Fe3O4 and raw CoFe-LDH11. Meanwhile, Fe3O4@CoFe-LDH11 displayed good adaptability in a wide pH range from 4 to 9 and relatively low PMS activation energy (39.9 kJ mol-1). The interference tests revealed HCO3 - to possess the strongest restriction effect. Only 57.7% AO7 was removed when 10 mM HCO3 - was introduced, which was ascribed to HCO3 - not only serving as a radical scavenger, but also increasing the pH of the system. The radical quenching tests demonstrated SO4˙- as the dominant reactive species during the catalytic reaction. Based on X-ray photoelectron spectroscopy (XPS) analysis, the core structure of Fe3O4 served as an electron donor for accelerating the cycle of Co(ii)/Co(iii) at the active site of the LDH outer shell. Also, Fe3O4@CoFe-LDH exhibited outstanding stability and recyclability, and maintained high degradation efficiency of AO7 even after five cycles. In sum, the proposed magnetic Fe3O4@CoFe-LDH nanocomposite has great potential for remediation of wastewater contaminated with synthetic dyes.

Phytoremediation of soil heavy metals (Cd and Zn) by castor seedlings: Tolerance, accumulation and subcellular distribution.

Cd and Zn pollution was observed to often occur simultaneously in soils. However, previous studies focused on single heavy metal instead of Cd and Zn combined pollution. Castor (Ricinus communis) is considered to have great potential for contaminated soil remediation. The resistance of castor seedlings to heavy metals and the mechanism behind it remain unknown. In this study, the tolerance and accumulation ability of castor seedlings to Cd and Zn were investigated, and the accumulation mechanism involving the subcellular distribution in different tissues was further explored. The results on biomass and chlorophyll revealed that castor seedlings have good tolerance to the pollution with 0-5 mg/kg Cd and 380 mg/kg Zn, while not to the heavy pollution with 25 mg/kg Cd and 380 mg/kg Zn. The maximum accumulation concentrations of Cd and Zn, 175.3 mg Cd/kg and 386.8 mg/kg Zn, appeared in castor seedling root instead of stem and leaf, indicating that root played a significant part in accumulating Zn and Cd. The relative low dosage of Cd (0-5 mg/kg) promoted the accumulation of Zn in the subcellular component, while high dosage (25 mg/kg) inhibited the accumulation of Zn. In subcellular accumulation and distribution of castor seedlings, Cd (27.1%-69.4%) and Zn (39.6%-66.6%) in the cell wall was the highest. With the increase of Cd addition, the accumulation of Cd increased in cell wall while decreased in organelle and soluble fraction. Hydroxyl, amino, amides and carboxyl functional groups on cell wall might provided the main binding sites for Cd and Zn.

Control of the Hydraulic Load on Nitrous Oxide Emissions from Cascade Reservoirs.

Nitrous oxide (N2O) emissions show large variability among dam reservoirs, which makes it difficult to estimate N2O contributions to global greenhouse gases (GHGs). Because river damming alters hydraulic residence time and water depth, the hydraulic load (i.e., the ratio of the mean water depth to the residence time) was hypothesized to control N2O emissions from dam reservoirs. To test this hypothesis, we investigated N2O fluxes and related parameters in the cascade reservoirs along the Wujiang River in Southwest China. The N2O fluxes showed obvious temporal and spatial variations, ranging from -7.86 to 337.22 µmol m-2 d-1, with an average of 12.76 µmol m-2 d-1. Nitrification was the main pathway of N2O production in these reservoirs, and seasonal dissolved oxygen (DO) stratification played an important role in regulating the N2O production. The reservoir N2O flux had a significant negative logarithmic relationship with the hydraulic load, suggesting its control of the N2O emission. This was because the hydraulic load was a prerequisite for regulating the nitrification-denitrification and the DO stratification in the dam reservoirs. This empirical relationship will help to estimate the contribution of reservoir N2O emissions to global GHGs.

Enhancement in adsorption potential of microplastics in sewage sludge for metal pollutants after the wastewater treatment process.

Microplastics (MPs) as new pollutants of environmental concern have been widely detected in sewage sludge, and may act as significant vectors for metal pollutants due to their adsorption property. Our findings show that Cd, Pb, and Co, but not Ni, contents in sewage sludge are lower than that of corresponding metal irons adsorbed on sludge-based MPs, indicating that the MPs accumulate such metal pollutants as Cd in the sludge samples. In contrast to virgin MPs, sludge-based MPs are one order of magnitude higher adsorption capacity for Cd, which reaches up to 2.523 mg g-1, implying that there is a considerable enhancement in adsorption potential of the MPs for metals after the wastewater treatment process. SEM analysis shows that sludge-based MPs have rougher and more porous surface than virgin MPs, and FTIR spectra reveal that functional groups such as CO and OH are found on sludge-based MPs. Further, two-dimensional FTIR correlation spectroscopy indicates that CO and NH functional groups play a vital role in the process that sludge-based MPs adsorb Cd, which are not found in virgin MPs. The results imply that increased adsorption potentials of the sludge-based MPs to Cd are attributed to changes in the MP physicochemical properties during wastewater treatment process. In addition, such factors as pH value, and sludge inorganic and organic components also have an effect on the MP adsorption to Cd. Principal component analysis shows that the MPs could be divided into three categories, i.e. polyamide, rubbery MPs (polyethylene and polypropylene) and glassy MPs (polyvinyl chloride and polystyrene). Their adsorption potentials to Cd follow the decreasing order: polyamide > rubbery MPs > glassy MPs. In summary, these findings indicate that MPs may exert an important influence on fate and transport of metal pollutants during sewage sludge treatment process, which deserves to be further concerned.

Interaction effects of oxytetracycline and copper at different ratios on marine microalgae Isochrysis galbana.

Contamination with both oxytetracycline (OTC) and Cu is prevalent in water. OTC can chelate with Cu to form OTC + Cu composites. Through the study of the effects of the interaction of OTC and Cu on the algae Isochrysis galbana at multiple coordination ratios, it was found that the OTC + Cu complex was antagonistic to algae growth after 24 h of exposure but was synergistic in treatment (T) 3 and T4 after 48 and 72 h. Compared with OTC alone, the addition of Cu addition significantly inhibited the biosynthesis of chlorophyll a, but the ratio (R) in the OTC + Cu and OTC treatments gradually increased from T1 to T4. The addition of Cu also led to a significant increase in malondialdehyde and reactive oxygen species, but R gradually decreased and increased, respectively, from T1 to T4. The accumulation of OTC in algae was considerably promoted by the addition of Cu, with R increasing 1.5 in T2 to 2.6 in T4; moreover, the residue of OTC in water was reduced in the presence of algae. OTC alone dramatically inhibited the absorption of Cu by algae, while in the presence of OTC + Cu, only the two high-OTC treatments showed a significant decrease in Cu absorption. In addition, the absorption of Mg was markedly inhibited in all OTC treatments and the adsorption of K in the high-OTC treatment, but these inhibitory effects were alleviated in the OTC + Cu treatment. These results indicated that the effects of the OTC + Cu complex on algae were different from the effects of OTC and Cu alone.

Determination of the phytoremediation efficiency of Ricinus communis L. and methane uptake from cadmium and nickel-contaminated soil using spent mushroom substrate.

Spent mushroom substrate (SMS) as an organic amendment to plant production has received increasing attention on soil phytoremediation. However, organic amendments are known to contribute to greenhouse gas (GHG) emission from soils. Castor oil plant has a high biomass production and phytoremediation potential for heavy metal-contaminated soils. In the present study, the roles of SMS on phytoremediation efficiency of castor oil plant (Ricinus communis L.) from cadmium (Cd) and nickel (Ni)-contaminated soils were investigated, and the impact of SMS application on methane emission from the contaminated soil were evaluated. Pot experiments with SMS-amended and unamended contaminated soils were conducted to investigate Cd and Ni accumulation in R. communis and CH4 emission. After growing for 3 months in soils with the addition of Cd (10 mg/kg) and Ni (at rates of 200 and 600 mg/kg), the dry biomass and the concentrations of Cd and Ni in the R. communis were measured, and the mobility factors for Cd and Ni were calculated. To assess methane emission, CH4 fluxes and potential rates of CH4 production and oxidation were measured pre- and post-incubation. SMS addition significantly improved the growth of R. communis and gave 19.15~82.46% more dry weight as compared to the single plant cultivation in the contaminated soils. SMS also increased plant Cd uptake and the total amount of Cd accumulation in R. communis increased by 28.1-152.1%, respectively, in signal Cd treatment and Cd-Ni complexation treatment, as compared to the single plant cultivation. The high values of mobility factor for Cd in single plant cultivation and co-application of SMS and R. communis pointed to the potential of R. communis to the Cd mobilization from the contaminated soils. Moreover, the addition of SMS tended to stimulate CH4 uptake that the average increases in CH4 uptake rate were 3.84-fold (in controls) and 2.91-fold (in single Cd treated soils) by the co-application of SMS and R. communis as compared to the single plant cultivation. The results suggested that the application of SMS could improve the growth of R. communis in Cd and Ni-contaminated soil, enhance heavy metal bioaccumulation, and stimulate soil CH4 uptake. Therefore, SMS might be useful for enhancing phytoremediation of heavy metals and mitigate CH4 emission from the contaminated soil. In addition, results in the study implied that implementing carefully designed management strategies (e.g., application of organic residues) during contaminated soil remediation is a promising solution for agricultural waste management and soil phytoremediation.

Comparative study of remediation of Cr(VI)-contaminated soil using electrokinetics combined with bioremediation.

The purpose of this research is to design a new bioremediation-electrokinetic (Bio-EK) remediation process to increase treatment efficiency of chromium contamination in soil. Upon residual chromium analysis, it is shown that traditional electrokinetic-PRB system (control) does not have high efficiency (80.26%) to remove Cr(VI). Bio-electrokinetics of exogenous add with reduction bacteria Microbacterium sp. Y2 and electrokinetics can enhance treatment efficiency Cr(VI) to 90.67% after 8 days' remediation. To optimize the overall performance, integrated bio-electrokinetics were designed by synergy with 200 g humic substances (HS) into the systems. According to our results, Cr(VI) (98.33%) was effectively removed via electrokinetics. Moreover, bacteria and humic substances are natural, sustainable, and economical enhancement agents. The research results indicated that the use of integrated bio-electrokinetics is an effective method to remediate chromium-contaminated soils.

N-fixing trees in wetland restoration plantings: effects on nitrogensupply and soil microbial communities.

To investigate the impact of an exotic Frankia nodulated tree (Alnus trabeculosa) on soil nitrogen content, soil microbial composition, and the abundance of N turnover-related functional microorganism community, we compared the community structure and abundance of key functional genes (nifH, bacterial/archaeal amoA, and nosZ) in the rhizosphere and nonrhizosphere of monoculture of Phragmites australis and A.trabeculosa-P.australis mixed communities by MiSeq Illumina sequencing and real-time PCR, respectively. The introduction of Frankia nodulated tree to recover degraded wetland was effective in the accumulation of soil organic carbon and nitrogen, which was the key factor to impact on the bacterial community composition revealed by canonical correspondence analysis. Acidobacteria and Proteobacteria were the dominant bacterial phylums while seven rare phyla appeared the most phylogenetically different among the investigated soil of two vegetations, including Chlorobi, Cyanobacteria, OD1, OP11, TM6, TM7, and GN02. The gene copy numbers of nifH were ranged from 2.28 × 108 to 2.96 × 109 copies g-1 dry soil in the wetland, and which were significantly higher in soil samples from P. australis than that from A.trabeculosa. While the abundance of nosZ in both rhizosphere and nonrhizosphere soils of A.trabeculosa-P.australis mixed communities was significantly lower compared with P.australis monoculture. The potential nitrification (PNA) (0.15-0.41 mg NOx-N kg-1 dry soil d-1) in the rhizosphere of A. trabeculosa was significantly higher than that of P. australis, and the soil denitrification enzyme activity (DEA) (0.42-0.90 nmol N2O-N g-1 dry soil h-1) was lower in the mixed community compared with monoculture of P. australis. The introduced planting of Frankia nodulated tree effectively accumulated soil organic carbon and nitrogen and reduce the relative abundance and activity of nitrogen-fixing bacteria and denitrification bacteria.

Combined remediation of pyrene-contaminated soil with a coupled system of persulfate oxidation and phytoremediation with ryegrass.

The in situ chemical oxidation technology (ISCO) and phytoremediation for PAHs have been studied respectively, but few focus on the feasibility of combining persulfate with ryegrass. This literature revealed the effect of persulfate oxidation on the growth of ryegrass and the removal ratios of pyrene in the couple system of persulfate oxidation and phytoremediation. The results demonstrated that half of pyrene in test soil was oxidized by persulfate in 7 days and then the residual pyrene concentration was decreased to a lower level by ryegrass in the following 2 months in oxidation treatment and drip washing and plants (OWP) and oxidation treatment and drip washing and plants and fertilization (OWFP) treatment. Ryegrass could grow well after persulfate oxidation with the oxidized soil washed by water. Ryegrass in OWP and OWFP treatments had higher ratios of overground and underground biomass. However, the seeds of ryegrass cannot germinate when drip washing was omitted. Pyrene together with residual persulfate changed soil enzyme activities. Drip washing and the growth of ryegrass made soil enzyme activities tend to returned to normal levels. Persulfate oxidation and phytoremediation were compatible to make contributions to the dissipation of pyrene. Persulfate oxidation activated by heat had higher removal efficiency of PAHs and phytoremediation could further decrease the pyrene concentration in spiked soil.