我国文化和旅游产业融合效率的时空动态演化及其驱动机理

采用仁慈型交叉DEA效率模型、冷热点分析、Tobit模型等方法对2010—2019年我国文化产业和旅游产业融合效率的时空动态演化及驱动机理进行了全面探析,结果发现:①2010—2019年我国文化产业和旅游产业融合效率呈波动上升趋势。②研究期内,文化和旅游产业融合效率呈“东部—中部—西部”依次递减,而融合效率增长率呈“东部—西部—中部”依次递减,但融合增长率都不高。③研究期内,文化产业和旅游产业融合效率呈区域差异性和集聚性。④从文化和旅游产业融合效率驱动机制剖析来看,经济发展、居民消费水平、地区城市化水平、信息发达程度、创新能力、政府政策支持力度是我国文化和旅游产业融合效率的驱动因素,促使效率时空动态演化。     

红色旅游资源数字化保护:理论认知与技术路径

中国特色社会主义进入新时期,红色旅游发展受到国家的高度重视,如何保护与利用红色旅游资源成为当前亟需探索的科学问题。结合信息空间理论,深入探究了红色旅游资源数字化保护的技术路径。结果表明:红色旅游资源数字化本质上是以数字形式保护并加以利用的知识转化过程,以此构建了红色旅游资源采集与保存、展示与传播、修复与传承、监测与管理的数字化保护路径。研究结果丰富了红色旅游资源数字化保护的理论支撑与架构体系,可为我国红色旅游资源数字化保护提供基础理论与技术范式参考。     

郑州与福州降水同位素特征及水汽来源对比分析

研究基于郑州与福州两地区GNIP(1985—1992年)大气降水同位素资料,对其大气降水同位素的季节变化以及环境因子进行比较分析。结果表明,郑州地区较福州地区季节变化明显,且两地区与温度和降水量均呈现负相关关系;根据两地区大气降水线方程得出,福州地区大气降水线方程斜率和截距大于郑州地区;两地区的d-excess值夏季高,冬季低;福州地区受台风影响,两地区降水量差别较大导致降水量在决定两地区月加权平均d-excess值时,福州地区整体比郑州地区偏大;采用MeteoInfo软件,并利用由美国国家大气研究中心所提供的气象资料,对两地区气团轨迹进行后向模拟,比较分析得出:郑州地区在夏季大部分水汽来自南海,春季、秋季和冬季的水汽均来自北方大陆;福州地区在夏季的水汽全部水汽来自低纬度的海洋,而春季、秋季和冬季的水汽仅有少部份来自北方大陆。     

济南市PM2.5中二次组分的时空变化特征及其影响因素

为分析济南市PM_2.5中二次组分的时空变化和影响因素,对济南市春季(2019年5月16—25日)、秋季(2019年10月15—24日)和冬季(2019年12月17—2020年1月16日)4个典型点位的PM_2.5样品进行连续采样,并测定了PM_2.5中水溶性离子、有机碳(OC)和元素碳(EC)的含量。结果表明:物流交通区的二次组分质量浓度最高(56.13μg·m^?3),钢铁工业区的二次组分浓度比城市市区高,但是二次组分占比较城市市区低,清洁对照点的浓度和占比最低;济南市4个功能区SO₄^2?和NO₃^?转化率均高于0.1,除清洁对照点外,城市市区、钢铁工业区和物流交通区的SO₄^2?转化率明显高于NO₃^?转化率;济南市春季、秋季和冬季的ρ(NO₃^?)/ρ(SO₄^2?)分别为0.67、2.57和1.98,春季PM_2.5浓度以固定源贡献为主,秋季和冬季以移动源贡献为主;运用ISORROPIA热力学模型分析了含水量和pH对二次组分生成的影响,含水量会随着污染增大而增大,酸度和含水量对二次无机组分的转化机理产生影响,酸度会抑制二次无机组分的生成,而含水量会促进二次组分的生成;后向轨迹聚类分析结果表明,占比最高的轨迹(29.2%)来自东北方向的滨州和东营,基于潜在源贡献因子(WPSCF)和浓度权重轨迹(WCWT)分析PM_2.5中二次组分质量浓度的潜在污染源区域,SO₄^2?的主要贡献源区在济南市区北部的济阳区和东北方向的滨州、东营等,NO₃^?和NH₄⁺的主要贡献源区在济南市区北方向的济阳区、东北方向的章丘区和南方向的莱芜区等。该研究结果可为中国北方城市细颗粒物进一步的治理和防控提供数据支撑和理论依据。     

Mechanistic insight into the biofilm formation and process performance of a passive aeration ditch (PAD) for decentralized wastewater treatment

• A Passive Aeration Ditch was developed to treat decentralized wastewater. • A model was developed to describe the process performance. • A high C/N ratio facilitates microbial growth but nitrification deteriorates. • A high salinity decreases both organic and nitrogen contaminants removal. Decentralized wastewater containing elevated salinity is an emerging threat to the local environment and sanitation in remote coastal communities. Regarding the cost and treatment efficiencies, we propose a passive aeration ditch (PAD) using non-woven polyester fabric as a feasible bubbleless aerator and biofilm carrier for wastewater treatment. Consideration has been first given to PAD’s efficacy in treating saline decentralized wastewater, and then to the impact of chemical oxygen demand-to-nitrogen (C/N) ratio and salinity on biofilm formation. A multispecies model incorporating the salinity effect has been developed to depict the system performance and predict the microbial community. Results showed that the PAD system had great capacity for pollutants removal. The biofilm thickness increased at a higher C/N ratio because of the boost of aerobic heterotrophs and denitrifying bacteria, which consequently improved the COD and total nitrogen removal. However, this led to the deterioration of ammonia removal. Moreover, while a higher salinity benefited the biofilm growth, the contaminant removal efficiencies decreased because the salinity inhibited the activity of aerobic heterotrophs and reduced the abundance of nitrifying bacteria inside the biofilm. Based on the model simulation, feed water with salinity below 2% and C/N ratio in a range of 1 to 3 forms a biofilm that can reach relatively high organic matter and ammonia removal. These findings not only show the feasibility of PAD in treatment of saline decentralized wastewater, but also offer a systematic strategy to predict and optimize the process performance.     

Product identification and toxicity change during oxidation of methotrexate by ferrate and permanganate in water

• Oxidation of methotrexate by high-valent metal-oxo species was first explored. • Fe(VI) presented a higher reactivity to MTX than Mn(VII) at pH 8.0. • Ketonization and cleavage of peptide bond were two initial reaction pathways. • Products of MTX were not genotoxic, neurotoxic, or endocrine-disrupting chemicals. • The less biodegradable products exhibited developmental and acute/chronic toxicity. Accompanying an annual increase in cancer incidence, the global use of anticancer drugs has remarkably increased with their worldwide environmental prevalence and ecological risks. In this study, the oxidation of methotrexate (MTX), a typical anticancer drug with ubiquitous occurrence and multi-endpoint toxicity, by ferrate(VI) (Fe(VI)) and permanganate (Mn(VII))) was investigated in water. Fe(VI) exhibited a higher reactivity with MTX (93.34 M⁻¹ s⁻¹) than Mn(VII) (3.01 M⁻¹ s⁻¹) at pH 8.0. The introduction of Cu(II) and Fe(III) at 1.0 mM improved the removal efficiency of 5.0 μM MTX by 100.0 μM Fe(VI) from 80% to 95% and 100% after 4 min, respectively. Seven oxidized products (OPs) were identified during oxidative treatments, while OP-191 and OP-205 were characterized as specific products for Fe(VI) oxidation. Initial ketonization of the L-glutamic acid moiety and cleavage of the peptide bond of MTX were proposed. Additionally, a multi-endpoint toxicity evaluation indicated no genotoxicity, neurotoxicity, or endocrine-disrupting effects of MTX and its OPs. Particularly, serious developmental toxicity in zebrafish larvae was observed in the treated MTX solutions. Based on the acute and chronic aquatic toxicity prediction, OP-190, OP-192, OP-206, and OP-208 were deemed toxic or very toxic compared to harmful MTX. Furthermore, the reduced biodegradability index from 0.15 (MTX) to −0.5 to −0.2 (OP-192, OP-206, and OP-468) indicated the formation of lower biodegradable OPs. Overall, this study suggests that Fe(VI) and Mn(VII) oxidation are promising treatments for remediating anticancer drug-contaminated water. However, the environmental risks associated with these treatments should be considered in the evaluation of water safety.     

High performance of multi-layered alternating Ni–Fe–P and Co–P films for hydrogen evolution

Judiciously engineering the electrocatalysts is attractive and challenging to exploit materials with high electrocatalytic performance for hydrogen evolution reaction. Herein, we successfully perform the interface engineering by alternately depositing Co–P and Ni–Fe–P films on nickel foam, via facile electroless plating and de-alloying process. This work shows that there is a significant effect of de-alloying process on alloy growth. The electronic structure of layered alloys is improved by interface engineering. The multilayer strategy significantly promotes the charge transfer. Importantly, the Co–P/Ni–Fe–P/NF electrode fabricated by interface engineering exhibits excellent electrocatalytic hydrogen evolution activity with an overpotential of 43.4 mV at 10 mA cm-2 and long-term durability for 72 h in alkaline medium (1 mol L-1 KOH). The innovative strategy of this work may aid further development of commercial electrocatalysts.     

Exploring the spatial pattern of renewable energy technology innovation: evidence from China

Environmental Science and Pollution Research - Considering the obvious regional differences in China, research on the drivers for renewable energy technology innovation (RETI) needs to fully...     

Impact of air pollutants on hospital visits for pediatric asthma in Fuzhou city,southeast China

Environmental Science and Pollution Research - Rapid social development in China has resulted in severe air pollution and adverse impacts on people’s health. Although studies have been...     

How does turions production of Potamogeton crispus L. respond to parental population biomass and living environment

Environmental Science and Pollution Research - Turions production is the dominant means of propagation in Potamogeton crispus L. To understand how parental population and their living environmental...