Co-Effects of Nitrogen Fertilizer and Straw-Decomposing Microbial Inoculant on Decomposition and Transformation of Field Composted Wheat Straw.

Although straw is an abundant and useful agricultural byproduct, it, however, exhibits hardly any decomposition and transformation. Despite the successful application of chemical and biological substrates for accelerating straw decomposition, the co-effects and mechanisms involved are still unknown. Herein, we performed a 120 day field trial to examine the co-effects of a nitrogen fertilizer (N) and a straw-decomposing microbial inoculant (SDMI) on the straw mass, nutrient release, and the straw chemical structure of composted wheat straw in the Chaohu Lake area, East China. For this purpose, four treatments were selected with straw: S (straw only), NS (N + straw), MS (SDMI + straw), and NMS (N + SDMI + straw). Our results indicated that NMS caused a higher straw decomposition rate than S, NS, and MS (p < 0.05) after 120 days of composting. The N, P, and K discharge rates in treating with NMS were higher than other the treatments at 120 days. The A/OA ratios of the straw residues were gradually increased during the composting, but the treatment of NMS and MS was lower than the CK at the latter stage. The RDA showed that the decomposition rate, nutrient release, and the chemical structure change in the straw were cumulative, while respiration was strongly correlated with lignin peroxidase, manganese peroxidase, and neutral xylanase. In conclusion, nitrogen fertilizer or straw-decomposing microbial inoculant application can improve the decomposition rate and nutrient release with oxidase activity intensified. However, the co-application of nitrogen fertilizer and a straw-decomposing microbial inoculant promoted straw decomposition and enzyme activity better than a single application and showed a lower decomposition degree, which means more potential for further decomposing after 120 days.

[Variations in Ozone Concentration in Seven Regions Under Different Temperature and Humidity Conditions].

In recent years, the situation of ozone pollution in China has become increasingly severe, with PM2.5 being the main pollutant in the atmospheric environment of several cities. Meteorological conditions, particularly temperature and humidity, have a great influence on ozone formation. Therefore, understanding and quantifying the impact of the variation in temperature and humidity on ozone level can effectively provide the theoretical basis for the government to prevent and control ozone pollution. By analyzing the relationship among the daily maximum temperature (Tmax), relative humidity (RH), and the maximum 8-h running average ozone (O3-8h) measured from January 1, 2015 to July 31, 2022, a linear positive correlation between O3-8h and Tmax was observed in the seven regions with serious ozone pollution, and the temperature penalty factor ranged from 2.1-6.0 µg·(m3·â„ƒ)-1; a nonlinear correlation between O3-8h and RH was also observed, and O3-8h was the highest when RH was 55%. The sensitivity of different regions to Tmax and RH was slightly different; generally, the most suitable meteorological conditions for ozone formation were 29℃ ≤ Tmax< 38℃ and 40% ≤ RH<70%. In the Yangtze River Delta, Jiangsu-Anhui-Shandong-Henan, and the middle reaches of the Yangtze River, under extreme high temperature conditions (Tmax ≥ 35℃), O3-8h stopped increasing with the increase in temperature and even dropped; simultaneously, it was often accompanied with a small increase in particulate matter. It may be related to the heterogeneous reaction of some precursors with higher water vapor content and the increase in ozone heterogeneous sink.

Synthetical effect of microplastics and chiral drug amphetamine on a primary food source algae Chlorella pyrenoids.

The biological effects and fate of the chiral illicit drug amphetamine in the presence and absence of microplastics on freshwater algae (Chlorella pyrenoids), including acute toxicity, growth inhibition, photosynthetic pigment content, oxidative stress, lipid peroxidation, and enantioselective fate were assessed. An agglomeration and the shading effects of microplastics in algae suspension were also determined. Microplastics were observed to increase the toxicity of amphetamine to algae and reduce algae cell growth. Exposed Chlorella pyrenoids exhibited a reduced algae cell counts in an agglomeration test, wherein algae cells decreased between 18% and 56% among treatment groups exposed to 5-50 mg L-1 of microplastics. The agglomeration test suggested that microplastics might significantly increase the adverse effect on algae. Furthermore, our experiments demonstrated enantioselective degradation of amphetamine in algae, and demonstrated that the S-enantiomer was preferably degraded by algae cells. Adding microplastics to the algae suspension significantly reduced the enantioselectivity, with an EF value of 0.41 compared with amphetamine-alone group (0.34) after 21 d exposure. These results demonstrated the first evidence of microplastics acting as a vehicle to enhance amphetamine toxicity to Chlorella pyrenoids, as well as provided new insights into the co-effect of microplastics and organic contaminants on food source.

[Carbon Dioxide Mitigation Co-effect Analysis of Structural Adjustment Measures in the "2+26" Cities in the Jing-Jin-Ji Region and Its Surroundings].

The Three-Year Action Plan for Winning the Blue Sky Defense Battle states that structural adjustments of industrial, energy, transportation, and land use are important to significantly reduce CO2 and air pollutant emissions. This co-effect is evident but has not been quantified at the city-cluster level. This study developed an emission inventory for the "2+26" cities of the Jing-Jin-Ji region and its surroundings and quantitatively analyzed the impacts of measures in the Three-Year Action Plan for Winning the Blue Sky Defense Battle on the emissions of CO2 and major air pollutants using Greenhouse Gas and Air Pollution Interactions and Synergies in the "2+26" cities model (GAINS-JJJ). The results showed that in the "2+26" cities, the emission reductions in CO2, primary PM2.5, SO2, NOx, and NH3 under policy scenario 2020 were 29.1 Mt (equivalent to 2% of the emissions in 2017), 203.8 (21%), 281.8 (27%), 485.5 (17%), and 34.3 kt (3%), respectively, relative to 2017. In terms of the cities or sectors, the higher the pollutant emissions, the higher the reduction achieved. The CO2 mitigation co-effect results showed that industrial adjustment measures, such as eliminating backward production capacity, upgrades on industrial boilers, and phasing out small and polluting factories, contributed the most to the co-effect of CO2 emission reduction, whereas NOx presented the highest co-effects, with CO2 among the different air pollutants.

Co-effect assessment on regional air quality: A perspective of policies and measures with greenhouse gas reduction potential.

Clean air policies have achieved remarkable air quality improvement in China for the last decade. However, as more importance was attached to climate issues and further improvement of air quality, policies with greenhouse gas (GHG) reduction potential were supposed to play a significant role. Here, we designed a conventional legislation pathway scenario (CLP) and an enhanced greenhouse gas reduction scenario (EGR), to estimate the co-effects of policies effective in GHG reduction on air pollutant control and air quality improvement in the Yangtze River Delta (YRD) region from 2014 to 2020, adopting a measure-specific evaluation method and an integrated WRF-CAMx model simulation. Results showed that: 1) With the implementation of enhanced measures with GHG reduction potential, emissions of SO2, NOx, PM2.5, PM10, VOCs and NH3 decreased by 16.4 %, 21.6 %, 18.6 %, 16.5 %, 23.9 % and 15.4 % in EGR scenario respectively, compared with CLP scenario. And the annual mean simulated concentrations of PM2.5, SO2 and NO2 of the YRD decreased by 11.2 %, 15.4 % and 20.6 %, respectively. 2) The average 8-h maxima (MDA8) concentration of O3 presented a slightly increasing trend under the impacts of measures with GHG reduction potential, which might be on account of the unbalanced control of NOx and VOCs, the two major precursors of O3. 3) Based on the source apportionment analysis, major partition of total ozone in the four receptors in YRD was from regional transportation, rather than local formation. And the major sectors contributing to ozone were industry and transportation sector. This study quantitatively assessed the co-benefits of GHG-control-effective policies and specific measures on air quality improvement, which would help to provide implications for future policy-making to achieve air pollution and climate change co-control.

Study on the co-effect of maifanite-based photocatalyst and humic acid in the photodegradation of organic pollutant.

In this study, the co-effect of clay mineral-based photocatalyst and humic acid on the photodegradation of dye was revealed for the first time. The clay mineral-based photocatalyst, maifanite/g-C3N4, was prepared using the co-calcining method. The physical and chemical properties of the maifanite/g-C3N4 photocatalysts with various ratios were characterized by multiple characterization methods, including SEM, XPS, BET, UV-Vis, FTIR, contact angle, and XRD. The respective degradation experiment of humic acid and RhB was performed using maifanite/g-C3N4 photocatalysts. The degradation process of mixture solution of humic acid and RhB was measured using EEM and UV-vis. The result indicates that in the presence of humic acid, low ratio of maifanite/g-C3N4 inhibits the production of by-products derived from the interaction of humic acid and the degradation of RhB. However, high ratio of maifanite/g-C3N4 is not conducive to the degradation of RhB. The ratio of 1:3 for maifanite/g-C3N4 is optimal for the photodegradation of RhB in the presence of humic acid. This article provides a new perspective to develop the co-effect of clay mineral and humic acid in the photodegradation of organic pollutant.

Bimetallic co-effect of Au-Pd alloyed nanoparticles on mesoporous silica modified g-C3N4 for single and simultaneous photocatalytic oxidation of phenol and reduction of hexavalent chromium.

Perception of surface plasmonic resonance in heterogeneous photocatalysis not only has impact on basic science of sustainable energy development, but also generates green technologies for wastewater treatment, selective oxidation and reduction reactions. In the present study Au/Pd bimetallic alloyed nanoparticles were effectively decorated on mesoporous silica modified g-C3N4 (graphitic carbon nitride) nanosheets by a simple one-pot calcinations strategy. The formation of Au/Pd alloyed nanoparticles has been supported by XRD, UV-vis DRS, TEM and XPS studies. The photocatalytic performance of the photocatalysts were investigated by performing tandem reaction for simultaneous oxidation of phenol and reduction of Cr (VI). The photocatalytic performances were found to be significant for either single phenol species or single Cr (VI), but quite appreciable photocatalytic performance was observed for a solution containing Cr (VI)-phenol mixture. The synergetic effect of Au/Pd alloyed nanoparticle and enhanced photocurrent (1.4 mA/cm2) generated by the nano-composite further supports the activity. The results of tandem reaction not only reveals the feasibility of carrying out degradation of two important pollutants simultaneously from waste water, but also gives us an enlightenment to efficiently degrade mixture of pollutants without using any additional chemical as trapping agent in the photocatalytic process.