Phosphate-solubilizing bacteria improve the antioxidant enzyme activity of Potamogeton crispus L. and enhance the remediation effect on Cd-contaminated sediment.

Phosphorus-solubilizing bacteria (PSB) assisted phytoremediation of cadmium (Cd) pollution is an effective method, but the mechanism of PSB-enhanced in-situ remediation of Cd contaminated sediment by submerged plants is still rare. In this study, PSB (Leclercia adecarboxylata L1-5) was inoculated in the rhizosphere of Potamogeton crispus L. (P. crispus) to explore the effect of PSB on phytoremediation. The results showed that the inoculation of PSB effectively improved the Cd extraction by P. crispus under different Cd pollution and the Cd content in the aboveground and underground parts of P. crispus all increased. The µ-XRF images showed that most of the Cd was enriched in the roots of P. crispus. PSB especially showed positive effects on root development and chlorophyll synthesis. The root length of P. crispus increased by 51.7 %, 80.5 % and 74.2 % under different Cd pollution, and the Ca/Cb increased by 38.9 %, 15.2 % and 8.6 %, respectively. Furthermore, PSB enhanced the tolerance of P. crispus to Cd. The contents of soluble protein, MDA and H2O2 in 5 mg·kg-1 and 7 mg·kg-1 Cd content groups were decreased and the activities of antioxidant enzymes were increased after adding PSB. The results showed that the application of PSB was beneficial to the in-situ remediation of submerged plants.

Tuning microscopic structure of La-MOFs via ligand engineering effect towards enhancing phosphate adsorption.

The selection of different organic ligands when synthesizing metal organic framework (MOFs) can change their effects on the adsorption performance. Here, four La-MOFs adsorbents (La-SA, La-FA, La-TA and La-OA) with different organic ligands and structures were synthesized by solvothermal method for phosphate adsorption, and the relationship between their adsorption properties and structures was established. Among four La-MOFs, their phosphate adsorption capacities and adsorption rates followed La-SA > La-FA > La-TA > La-OA. The results indicated that average pore diameter played a key role in phosphate adsorption and there was a positive correlation between average pore diameter and adsorption capacity (R2 = 0.86). Coexisting ion experiments showed that phosphate adsorptions on three La-MOFs (La-SA, La-FA and La-TA) were inhibited in the presence of CO32- and HCO3-. The inhibition of CO32- was the most pronounced and the results of redundancy analysis pointed out that it was mainly due to the change of pH value. In contrast, La-OA showed enhanced phosphate adsorption in the presence of CO32- and HCO3-, and the combination of pH experiments showed that phosphate adsorption by La-OA was increased under alkaline conditions. Further combined with FT-IR, XRD, high resolution energy spectra of XPS (La 3d, P 2p and O 1s) and XANES, the adsorption mechanisms were derived electrostatic attraction, chemical precipitation and inner sphere complexation, and the last two were identified as the main mechanisms. Moreover, it can be identified from XPS 2p that the phosphate adsorption on La-FA and La-OA were mainly in the LaPO4 state, while La-SA and La-TA mainly existed in the form of LaPO4·xH2O crystals and inner sphere complexes. From the perspective of material morphology, this work provides a thought for the rational design of MOFs with adjustable properties for phosphate adsorption.

Dynamic characteristics of net anthropogenic phosphorus input to the upper Yangtze River Basin from 1989 to 2019: Focus on the phosphate ore rich area in China.

Phosphorus (P), a non-renewable essential resource, faces heavy exploitation and contributes to eutrophication in aquatic environments. Assessing P input is vital for a healthier P cycle in the Upper Yangtze River (UYR), a phosphate ore rich basin, where P mining and P chemical enterprises have prominent pollution problems. This study modified the net anthropogenic phosphorus input (NAPI) model to include ore mining P input (Pore). We analyzed the evolutionary characteristics of P input in five sub-basins of UYR from 1989 to 2019 using prefecture-level data, and assessed the uncertainty of the data. NAPI in all sub-basins exhibited an upward and then downward trend during 1989-2019, with the inflection point occurring in 2015 or 2016, showing a net increase of about 1.1 times (568-1162 kg P km-2 yr-1) in the whole UYR basin. Among the components of NAPI, P fertilizer inputs (Pfer) and food/non-food and feed P inputs (Pf/nf&feed) contributed comparably, though the growth rate of Pfer was most notable basin-wide. Pore proportion increased significantly (about 3-fold), with a peak of 20%, especially in Wujiang sub-basin. The multi-year (1989-2019) average NAPI in UYR rose sequentially from west to east, with hotspot areas mainly concentrated in the Sichuan-Chongqing urban agglomeration and cities of Hubei province. The regional P input closely related to the population density and the level of agricultural development, certainly the phosphate mining was also unignorable. This study emphasizes that based on current status of NAPI development in UYR, targeted management for different regions should focus on improving agricultural P use efficiency and rational exploitation of P mineral resources.

Bioremediation system consisted with Leclercia adecarboxylata and nZVI@Carbon/Phosphate for lead immobilization: The passivation mechanisms of chemical reaction and biological metabolism in soil.

Bioremediation is one of the most promising strategies for heavy metal immobilization. A new remediation system was demonstrated in this research, which combined phosphate solubilizing bacteria (PSB) with nZVI@Carbon/Phosphate (nZVI@C/P) composite to remediate lead contaminated soil. Experimental results indicated that the new system (nZVI@C/P + PSB) could effectively convert the labile Pb into the stable fraction after 30 days of incubation, which increased the maximum residual fraction percentage of Pb by 70.58%. The characterization results showed that lead may exist in the forms of Pb5(PO4)3Cl, PbSO4 and 3PbCO3·2Pb(OH)2·H2O in the soil treated with nZVI@C/P + PSB. Meanwhile, soil enzyme activities and Leclercia abundance were enhanced in the treated soil compared with CK during the incubation time. In addition, the specialized functions (e.g. ABC transporters, siderophore metabolism, sulfur metabolism and phosphorus metabolism) in PSB and nZVI@C/P + PSB group were also enhanced. These phenomena proved that the key soil metabolic functions may be maintained and enhanced through the synergistic effect of incubated PSB and nZVI@C/P. The study demonstrated that this new bioremediation system provided feasible way to improve the efficacy for lead contaminated soil remediation.

Anaerobic syntrophic system composed of phosphate solubilizing bacteria and dissimilatory iron reducing bacteria induces cadmium immobilization via secondary mineralization.

Secondary mineralization is a promising method for remediating cadmium (Cd) pollution in sediments, but the poor stability of Cd-containing secondary minerals is a bottleneck that limits the development of this approach. The existence of phosphate can enhance the formation of stable secondary minerals and points a new direction for Cd immobilization. In this research, a novel syntrophic system composed of phosphate solubilizing bacteria (PSB) and dissimilatory iron reducing bacteria (DIRB) was established and the effect and mechanism of Cd immobilization in the system were also explored. The results showed that under the conditions of DIRB:PSB (V:V)= 3:1, syntrophic bacteria dosage of 5% and glucose dosage of 5 g/L, Cd incorporated in the secondary minerals could account for about 60% of the total Cd. In the pH range of 5-9, alkaline environment was conducive to the immobilization of Cd and the percentage of combined Cd was up to 58%, while the combined Cd in secondary minerals decreased from 62% to 56% with the increase of initial Cd concentration from 0.1 to 0.3 mmol/L. In addition, XRD, XPS, Mössbauer and other characterization results showed that secondary minerals, such as Cd exchange hydroxyapatite (Cd-HAP) and kryzhanovskite (Fe3(PO4)2(OH)3) were formed in this new system. The established syntrophic system of PSB and DIRB is thus a prospective bioremediation technology for Cd immobilization in sediments and can avoid the potential risk might be caused by the addition of phosphorus-containing materials.

Humic acid and fulvic acid facilitate the formation of vivianite and the transformation of cadmium via microbially-mediated iron reduction.

The effects of humic acids (HA) and fulvic acids (FA) on the fate of Cd in anaerobic environment upon microbial reduction of Cd-bearing ferrihydrite (Fh) with Geobacter metallireducens were investigated. The results showed that HA and FA could promote the reductive dissolution of Fh and the formation of vivianite. After incubation of 38 d, vivianite accounted for 47.19%, 59.22%, and 48.53% of total Fe in biological control batch (BCK), HA and FA batches (C/Fe molar ratio of 1.0), respectively, by Mössbauer spectroscopy analysis. In terms of Cd, HA and FA could promote the release of adsorbed Cd during the initial bioreduction process, but reassuringly, after 38 d the dissolved Cd with HA and FA addition batches were 0.58-0.91 and 0.99-1.08 times of the BCK, respectively. The proportions of residual Cd in HA batches were higher than FA and BCK batches, indicating that HA was better than FA in immobilizing Cd. This might be because the quinone groups in HA could act as electron shuttle. This study showed that HA facilitated the transformation of vivianite better than FA, and Cd can be stabilized by resorption or co-precipitation with vivianite, providing a theoretical support for the translocation of Cd in sediment-water interface.

Boosting CO2 hydrogenation to methane over Ni-based ETS-10 zeolite catalyst.

The activation and conversion of the CO2 molecule have always been the most vexing challenge due to its chemical inertness. Developing highly active catalysts, which could overcome dynamic limitations, has emerged as a provable and effective method to promote CO2 activation-conversion. Herein, ETS-10 zeolite-based catalysts, with active nickel species introduced by in situ doping and impregnation, have been employed for CO2 methanation. Conspicuous CO2 conversion (39.7%) and perfect CH4 selectivity (100%) were achieved over the Ni-doped ETS-10 zeolite catalyst at 280°C. Comprehensive analysis, which include X-ray diffraction, N2 adsorption-desorption, SEM, TEM, H2 chemisorption, CO2 temperature programmed desorption, and X-ray photoelectron spectroscopy, was performed. Also, the results indicated that the resultant hierarchical structure, high metal dispersion, and excellent CO2 adsorption-activation capacity of the Ni-doped ETS-10 zeolite catalyst played a dominant role in promoting CO2 conversion and product selectivity.

Dispersive 2D Triptycene-Based Crystalline Polymers: Influence of Regioisomerism on Crystallinity and Morphology.

The merging of good crystallinity and high dispersibility into two-dimensional (2D) layered crystalline polymers (CPs) still represents a challenge because a high crystallinity is often accompanied by intimate interlayer interactions that are detrimental to the material processibility. We herein report a strategy to address this dilemma using rationally designed three-dimensional (3D) monomers and regioisomerism-based morphology control. The as-synthesized CPs possess layered 2D structures, where the assembly of layers is stabilized by relatively weak van der Waals interactions between C-H bonds other than the usual π-π stackings. The morphology and dispersibility of the CPs are finely tuned via regioisomerism. These findings shed light on how to modulate the crystallinity, morphology, and ultimate function of crystalline polymers using the spatial arrangements of linking groups.

Intra-/extra-cellular antibiotic resistance responses to sewage sludge composting and salinization of long-term compost applied soils.

Municipal sewage sludge, a reservoir of antibiotic resistance genes (ARGs), is usually composted as fertilizer for agricultural application especially in arid and semi-arid areas. The evolution patterns of intracellular ARGs (iARGs) and extracellular ARGs (eARGs) during composting and their responses to soil salinization after long-term compost application kept unclear previously, which were systematically studied in the current study. The variation and dissemination risk of eARGs and iARGs with the salinization of farmland soils was also evaluated. Extra/intra-cellular ARGs relative abundance varied drastically through composting process. Generally, the relative abundance of the cell-free eARGs (f-eARGs) and the cell-adsorbed eARGs (a-eARGs) were 4.62 and 3.54 folds (median) higher than that of iARGs, respectively, during the entire composting process, which held true even before the sludge composting (false discovery rate, FDR p < 0.05). There was no significant difference in relative abundance between f-eARGs and a-eARGs. The relative abundance of eARGs gradually decreased with composting time but was relatively higher than iARGs. It was worth noting that iARGs rebounded in the maturation phase. However, an over ten-year application of the eARG-rich compost led to much more severe contamination of iARGs than eARGs in soil. Soil salinization caused remarkable rise of eARGs by 943.34-fold (FDR p < 0.05). The variation of ARGs during composting and soil salinization was closely related to the change of microbial community structure. In compost, the bacterial communities mainly interacting with ARGs were the Firmicutes (54 unique and 35 shared core genera); and the bacterial communities playing major roles in ARGs during soil salinization were Proteobacteria (116 unique and 53 shared core genera) and Actinobacteria (52 unique and 27 shared core genera). These findings are important for assessing the transmission risk of ARGs in compost application to farmland in arid and semi-arid areas.

Efficient phosphorus recovery as struvite by microbial electrolysis cell with stainless steel cathode: Struvite purity and experimental factors.

Phosphorus (P) recovery from waste streams is an essential choice due to the coming global P crisis. One promising solution is to recover P by microbial electrolysis cell (MEC). Both the P recovery effectiveness and product quality are of critical importance for application. In this study, a two-chamber MEC was constructed and the effects of applied voltage, NaAc concentration, Mg/P molar ratio, N/P molar ratio, and initial P concentration on P recovery and product purity were explored. The maximum P recovery efficiency of 99.64 % and crystal accumulation rate over 106.49 g/m3-d were achieved. Struvite (MAP) was confirmed as the final recovered product and the purity obtained could reach up to 99.95 %. Besides, higher applied voltage, N/P molar ratio and initial P concentration could promote P recovery efficiency, while the purity of MAP showed correlation with applied voltage, Mg/P molar ratio, N/P molar ratio and initial P concentration. The correlation between NaAc concentration and both of the above was not very significant. A lower energy consumption of 4.1 kWh/kg P was observed at the maximum P recovery efficiency. In addition, the efficiency of P recovery from real wastewater also could reach nearly 88.25 %. These results highlight the promising potential of efficient phosphorus recovery from P-rich wastewater by MEC.

Noval porous phosphate-solubilizing bacteria beads loaded with BC/nZVI enhanced the transformation of lead fractions and its microecological regulation mechanism in soil.

Soil lead pollution becomes a serious environmental problem. Microbial remediation has received widespread attentions due to high efficiency and no secondary pollution. In this research, a noval porous spherical phosphate-solubilizing bacteria bead loaded with biochar/nZVI (Bio-bead) was used to passivate lead in soil, and the effects and microecological regulation mechanisms of this process were also investigated. The results showed that the pH, OM, and AP of soil in the Bio-bead group were increased and the ORP was decreased over time compared with the blank group. The proportion of stable (oxidizable and residue) fractions of lead in Bio-bead group (45%) was much higher than that of the blank group (35%). In addition, the result of microbial community structure showed that Bio-beads did not change the species of dominant bacterial, excepting the abundance of Pseudomonas increased significantly and the abundance of Sphingomonas reduced during remediation. Redundancy analysis showed that pH, OM, AP and the ratio of residual and oxidizable fractions lead in soil were positively correlated with the abundance of Pseudomonas, while ORP was negatively correlated with the abundance of Pseudomonas. These findings have proved that Bio-bead is a potential strategy for remediation of lead-contaminated soil even in complexed soils.

Trehalose Regulates Starch, Sorbitol, and Energy Metabolism to Enhance Tolerance to Blue Mold of "Golden Delicious" Apple Fruit.

The efficacy of trehalose on the lesion diameter of apples (cv. Golden Delicious) inoculated with Penicillium expansum was evaluated to screen the optimal concentration. The changes in gene expression and activity of the enzyme in starch, sorbitol, and energy metabolism were also investigated in apples after trehalose treatment. The results revealed that trehalose dipping reduced the lesion diameter of apples inoculated with P. expansum. Trehalose suppressed the activities and gene expressions of ß-amylase, NAD-sorbitol dehydrogenase, and NADP-sorbitol dehydrogenase, whereas it decreased the sorbitol 6-phosphate dehydrogenase gene expression and amylose, amylopectin, total starch, and reducing sugar contents. Additionally, trehalose improved the gene expressions and activities of α-amylase, starch-branching enzymes, total amylase, H+-ATPase, and Ca2+-ATPase, as well as soluble sugar, adenosine triphosphate, and adenosine diphosphate contents and energy charge in apples. These findings imply that trehalose could induce tolerance to the blue mold of apple fruit by regulating starch, sorbitol, and energy metabolism.

Reactivity triggered by an organic microcrystal interface: a case study involving an environmentally benign, aromatic boric acid reaction.

A novel reactivity-triggering strategy for inert organic molecules was developed via the chemical properties of a crystal-solution interface. Upon self-assembling to form a {002} crystal interface, inactive 9-anthracene boric acid was transformed into an ultra-high active state, triggering a catalyst-free, environmentally benign, aromatic substitution and oxidation reaction, which achieved 99% yield in 1 h under ambient conditions.

Mitigation of methylmercury production in eutrophic waters by interfacial oxygen nanobubbles.

In mercury (Hg)-polluted eutrophic waters, algal blooms are likely to aggravate methylmercury (MeHg) production by causing intensified hypoxia and enriching organic matter at the sediment-water interface. The technology of interfacial oxygen (O2) nanobubbles is proven to alleviate hypoxia and may have potential to mitigate the risks of MeHg formation. In this study, incubation column experiments were performed using sediment and overlying water samples collected from the Baihua Reservoir (China), which is currently suffering from co-contamination of Hg and eutrophication. The results indicated that after the application of O2 nanobubbles, the %MeHg (ratio of MeHg to total Hg) in the overlying water and surface sediment decreased by up to 76% and 56% respectively. In addition, the MeHg concentrations decreased from 0.54 ± 0.15 to 0.17 ± 0.01 ng L-1 in the overlying water and from 56.61 ± 9.23 to 25.48 ± 4.08 ng g-1 in the surface sediment. The decline could be attributed to the alleviation of anoxia and the decrease of labile organic matter and bioavailable Hg. In addition, hgcA gene abundances in the overlying water and surface sediment decreased by up to 69% and 44% after the addition of O2 nanobubbles, as is consistent with MeHg occurrence in such areas. Accordingly, this work proposed a promising strategy of using interfacial oxygen nanobubbles to alleviate the potentially enhanced MeHg production during algal bloom outbreaks in Hg-polluted eutrophic waters.

Interfacial oxygen nanobubbles reduce methylmercury production ability of sediments in eutrophic waters.

Eutrophication can induce hypoxia/anoxia and rich organic matter at the sediment-water interface in surface waters. When eutrophic waters are impacted with mercury (Hg) pollution, methylmercury (MeHg) production ability (MPA) of surface sediment would increase and more MeHg might be produced. To tackle this risk, this study firstly collected samples of surface sediment and overlying water from a typical eutrophic lake-Taihu Lake. Then from a sediment-water simulation system, we demonstrated that eutrophic waters were able to methylate Hg spontaneously, and that sediment is the major Hg sink in the system. After the addition of HgCl2 solution (approximately 1 mg L-1 in the slurry), MeHg concentrations in the sediment increased by 11.7 times after 48 h. The subsequent column experiments proved that O2 nanobubbles could significantly decrease the MPA of surface sediment, by up to 48%. Furthermore, we found that O2 nanobubbles could remediate anoxia mainly by increasing dissolved oxygen (from 0 to 2.1 mg L-1), oxidation-reduction potentials (by 37% on average), and sulfate (by 31% on average) in the overlying water. In addition, O2 nanobubbles could also help decrease organic matter concentration, as was revealed by the decline of dissolved organic carbon in the overlying water (by up to 57%) and total organic carbon in surface sediment (by up to 37%). The remediation of anoxia and reduction of organic matter could contribute to the decrease of hgcA gene abundance (by up to 86%), and thus result in the reduction of MPA after the addition of O2 nanobubbles. This study revealed the risk of MeHg production in case Hg pollution occurs in eutrophic waters and proposed a feasible solution for MeHg remediation.

Retraction Note: Simulation and spatiotemporal pattern of air temperature and precipitation in Eastern Central Asia using RegCM.

This paper has been retracted.

Self-Stabilized Amorphous Organic Materials with Room-Temperature Phosphorescence.

The stability of pure organic room-temperature phosphorescent (RTP) materials in air has been a research hotspot in recent years. Without crystallization or encapsulation, a new strategy was proposed to obtain self-stabilized organic RTP materials, based on a complete ionization of a photo-induced charge separation system. The ionization of aromatic phenol 4-carbazolyl salicylaldehyde (CSA) formed a stable H-bonding anion-cation radical structure and led to the completely amorphous CSA-I film. Phosphorescent lifetimes as long as 0.14 s at room temperature and with direct exposure to air were observed. The emission intensity was also increased by 21.5-fold. Such an amorphous RTP material reconciled the contradiction between phosphorescence stability and vapor permeability and has been successfully utilized for peroxide vapor detection.

Optimization of pretreatment procedure for MeHg determination in sediments and its applications.

Methylmercury (MeHg) in sediment is difficult to be determined due to its low concentration and binding compounds like sulfide and organic matter. Moreover, wet sediment samples have been suggested to behave differently from certified reference materials in MeHg analysis. Optimal pretreatment procedure for MeHg determination in sediments has not been ascertained and whether the procedure could apply to sediment samples with complex matrix merits further research. This work firstly compared recovery results of five pretreatment procedures for MeHg determination using ERM-CC580. Using the optimal pretreatment procedure, recovery results were analyzed in different sediment samples after manipulation of moisture content, organic matter, and acid volatile sulfide. The procedure using CuSO4/HNO3 as leaching solutions and mechanical shaking as extraction method was proved to produce the most satisfactory recovery results (100.67 ± 6.75%, mean ± standard deviation). And when moisture content varied from 20 to 80%, average recovery results in sediment samples ranged from 100 to 125%. Furthermore, before and after the manipulation of organic matter or acid volatile sulfide, spiking recovery results varied little and were all within acceptable limit (85~105%). Therefore, the procedure of CuSO4/HNO3-mechanical is proposed as a universal pretreatment method for MeHg determination in sediment samples with various characteristics.

Visual Exploration of Neural Document Embedding in Information Retrieval: Semantics and Feature Selection.

Neural embeddings are widely used in language modeling and feature generation with superior computational power. Particularly, neural document embedding - converting texts of variable-length to semantic vector representations - has shown to benefit widespread downstream applications, e.g., information retrieval (IR). However, the black-box nature makes it difficult to understand how the semantics are encoded and employed. We propose visual exploration of neural document embedding to gain insights into the underlying embedding space, and promote the utilization in prevalent IR applications. In this study, we take an IR application-driven view, which is further motivated by biomedical IR in healthcare decision-making, and collaborate with domain experts to design and develop a visual analytics system. This system visualizes neural document embeddings as a configurable document map and enables guidance and reasoning; facilitates to explore the neural embedding space and identify salient neural dimensions (semantic features) per task and domain interest; and supports advisable feature selection (semantic analysis) along with instant visual feedback to promote IR performance. We demonstrate the usefulness and effectiveness of this system and present inspiring findings in use cases. This work will help designers/developers of downstream applications gain insights and confidence in neural document embedding, and exploit that to achieve more favorable performance in application domains.

Hypoxia Remediation and Methane Emission Manipulation Using Surface Oxygen Nanobubbles.

Algal blooms in eutrophic waters often induce anoxia/hypoxia and enhance methane (CH4) emissions to the atmosphere, which may contribute to global warming. At present, there are very few strategies available to combat this problem. In this study, surface oxygen nanobubbles were tested as a novel approach for anoxia/hypoxia remediation and CH4 emission control. Incubation column experiments were conducted using sediment and water samples taken from Lake Taihu, China. The results indicated that algae-induced anoxia/hypoxia could be reduced or reversed after oxygen nanobubbles were loaded onto zeolite micropores and delivered to anoxic sediment. Cumulated CH4 emissions were also reduced by a factor of 3.2 compared to the control. This was mainly attributed to the manipulation of microbial processes using the surface oxygen nanobubbles, which potentially served as oxygen suppliers. The created oxygen-enriched environment simultaneously decreased methanogen but increased methanotroph abundances, making a greater fraction of organic carbon recycled as carbon dioxide (CO2) instead of CH4. The CH4/CO2 emission ratio decreased to 3.4 × 10-3 in the presence of oxygen nanobubbles, compared to 11 × 10-3 in the control, and therefore the global warming potential was reduced. This study proposes a possible strategy for anoxia/hypoxia remediation and CH4 emission control in algal bloom waters, which may benefit global warming mitigation.