不同粒径纳米TiO2对大型溞的毒性效应及腐殖酸的调控作用

为评估纳米TiO₂在环境水体中的暴露风险,选用大型溞作为模式生物,研究了不同粒径纳米TiO₂（20、40、60和100 nm）对大型溞毒性效应的影响,并探究了腐殖酸对不同粒径纳米TiO₂毒性效应的调控作用.结果表明,粒径是影响纳米TiO₂颗粒毒性效应的重要因素,以大型溞半数致死时间（LT₅₀）为指标,不同粒径纳米TiO₂对大型溞的毒性作用强弱顺序依次为：20 nm颗粒 > 40 nm颗粒 > 60 nm颗粒 > 100 nm颗粒（p<0.05）.腐殖酸的存在可以显著降低纳米TiO₂颗粒对大型溞的毒性作用,腐殖酸对小尺寸纳米TiO₂颗粒的毒性抑制作用更为明显（p<0.05）.大型溞体内ROS水平与抗氧化系统相关酶活分析表明,纳米TiO₂导致大型溞体内活性氧自由基（ROS）浓度升高是其产生毒性作用的重要原因,腐殖酸的存在可以显著降低大型溞体内由于纳米TiO₂暴露而引起的ROS浓度上升（p<0.05）,进而减轻纳米TiO₂对大型溞的毒性作用.此外,腐殖酸可以减小不同粒径纳米TiO₂之间的毒性差异.本研究结果可为纳米TiO₂在环境水体中的暴露风险评估提供参考依据.     

景区动态承载力估算方法及其应用

景区承载力是旅游学研究的重要领域,由于现有景区承载力估算模型以景区由“均质的可游览空间”构成为假设前提,通过面积和游客单位游览面积进行景区承载力的估算,未涉及游客进入景区游览行为的动态性。由于游客不能瞬时填满整个景区,景区承载力具有时空特性,故建立景区动态承载力计算的概念模型,并构建以停留区、通道以及出入口等要素为空间实体的网络结构逻辑模型,从而提出基于网络结构的景区动态承载力估算方法,选取南京总统府景区作为实验区域,验证所提出的模型和算法。将地理信息科学应用于旅游管理,有利于确定景区承载力的具体量化水平,使景区管理分时管控措施得到有效发挥,进而促进旅游景区实现更高质量的经济社会效益。     

全球化变革下的中国对外自然资源流动及其关键研究问题

应对全球化变革及其不确定性,认识中国对外自然资源流动的特征与问题,是保障国家资源安全的基础,对实现高质量、可持续发展有重要意义。对应国际劳动分工从产业间贸易、产业内贸易到全球价值链的不同阶段,理解中国对外自然资源流动有不同的理论视角。现有研究主要关注自然资源以原始形态和制成品中的隐含形态在国家之间的流动,讨论了中国对外自然资源流动在供给与需求、利用强度与效率、资源禀赋与流向,以及全局与局部影响之间的矛盾。未来研究仍面临理论和现实的挑战。在理论方面,适应全球价值链分工发展,引入全球生产网络理论探讨企业间互动关系如何塑造自然资源流动路径,能更好地适应中国从“引进来”向“走出去”的转变,以及当下自然资源综合治理的研究需求。在现实方面,应对日益增强的不确定性,亟需深化对自然资源流动网络韧性,以及“双循环”互促关系的认识。     

中央苏区红色旅游资源跨区域整合开发研究：文化生态学视角

红色旅游资源是革命精神的核心载体,其保护和旅游利用面临着破碎化、片段化、静态化等问题,亟需开展整合开发研究。以中央苏区核心区为例,基于文化生态学理论,采用GIS空间分析方法和修正的引力模型,研究红色旅游资源空间格局和文化生态变迁,在此基础上提出整合开发的策略,结论如下：（1）红色旅游资源点空间上呈现局部聚集特征,赣南苏区形成章贡区、瑞金市、于都县“金三角”分布格局,闽西苏区则形成新罗区、永定区、上杭县、连城县“银菱形”分布格局;（2）闽西和赣南苏区各重大事件红色旅游资源点在空间上8.9~106.6 km的范围内,形成带状或面状的文化生态基底,并呈现一致向服务业主导型转变的发展态势;（3）红色旅游资源网络联系方向与服务业主导型文化生态方向错位发展,这是赣南和闽西红色旅游资源内部网络联系度较强,跨区域网络联系度较弱的重要原因。在此基础上,遵循红色旅游资源文化生态空间一体化、文化生态演变全域化、文化生态发展动态化的原则,提出空间集聚区优先整合开发、高发展指数红色旅游资源跨省域优先整合开发、跨主导类型关键节点优先整合开发三个整合开发对策,以期促进中央苏区红色旅游高质量发展。     

氯和紫外消毒过程中胞外抗性基因的产生特征

考察了城市污水氯和紫外消毒过程中不同物理形态的胞外抗性基因的产生行为与及微生物群落的关联特征.结果表明,氯消毒尽管使胞内抗性基因丰度下降,但使结合型胞外抗性基因丰度明显上升（0.7±0.1）log,而游离型胞外抗性基因丰度下降（0.2±0.1）log.紫外消毒也使胞内抗性基因下降,但使游离型胞外抗性基因显著上升（0.4±0.2）log,而结合型胞外抗性基因丰度下降（0.3±0.1）log.氯消毒后,结合型胞外DNA（a-eDNA）中变形菌门丰度下降而其他菌门的丰度上升,细菌多样性指数由4.2上升到4.7;而游离型胞外DNA（f-eDNA）中变形菌门上升了6.6%,多样性指数则从3.5降低到2.8.紫外消毒后,a-eDNA中变形菌门丰度下降了36.6%,多样性则上升到4.8,而f-eDNA中细菌丰度变化较小.分子生态网络分析揭示了抗性基因与细菌间广泛的寄存关系,tetA、tetX、sulI和sulII分别与17、15、15和5种菌属间存在共现性,表明抗性基因潜在宿主的变化是导致消毒后胞外抗性基因产生的关键原因.本研究表明氯和紫外消毒不能消除抗性基因风险,反而通过导致不同胞外抗性基因的大量产生,使风险的形式发生变化.     

兼氧条件下厨余垃圾发酵液作碳源的反硝化性能

在兼氧条件下,利用厨余垃圾厌氧发酵液调节反硝化系统的碳氮比（COD/TN,C/N）,并考察了其脱氮性能.结果表明,不同C/N条件下,反应系统均未出现有机物的积累,但高C/N条件下的亚硝酸盐最大积累浓度和积累速率高于低C/N;随着进水C/N的增大,反应整体脱氮率和反硝化速率不断增大,当C/N为13时,反硝化速率达到了最大值,为9.79mg/（gVSS·h）,其脱氮率超过95%;相同C/N条件下,反硝化速率和最大亚硝酸盐积累浓度均与进水硝酸盐浓度成正比.此外,实验结果表明,兼氧条件下的反硝化过程虽不易出现COD残留,但去除单位氮所需的有机物更多,且整体反硝化速率以及亚硝酸盐还原速率均低于厌氧条件.     

多元复合调理剂对镉砷污染农田土壤微生物群落结构的影响

通过温室盆栽试验,研究多元复合调理剂（石灰石、铁粉、硅肥和钙镁磷肥,简称LISP）对土壤基本理化性质、Cd和As的生物有效性和微生物群落结构的影响.结果表明,LISP可改变土壤基本理化性质,降低土壤有效态Cd和As含量,并改变土壤微生物群落结构.在0.4%的LISP添加下,土壤pH值、有效磷和总磷含量较CK处理分别显著（P< 0.05）提高0.57单位、130.6%和18.38%,同时土壤有效态Cd和As含量较对照分别显著（P< 0.05）降低21.76%和16.39%.高通量测序结果表明,添加LISP可维持污染土壤中正常微生物群落的多样性和丰富度,而显著改变土壤微生物群落的组成和结构,其中厚壁菌门、放线菌门和浮霉菌门等门水平物种的相对丰度增加,而绿弯菌门、酸杆菌门和疣微菌门等门水平物种的相对丰度降低.冗余分析和Mantel检验分析表明,土壤pH值、有效磷以及有效态Cd和As含量是影响土壤微生物群落结构的主要环境因子.上述结果表明,LISP是一种有效的、生态安全的调理剂用于农田土壤Cd和As污染土壤修复.     

Efficient degradation of Rhodamine B by magnetically recoverable Fe3O4-modified ternary CoFeCu-layered double hydroxides via activating peroxymonosulfate

Environment-friendly nano-catalysts capable of activating peroxymonosulfate (PMS) have received increasing attention recently. Nevertheless, traditional nano-catalysts are generally well dispersed and difficult to be separated from reaction system, so it is particularly important to develop nano-catalysts with both good catalytic activity and excellent recycling efficiency. In this work, magnetically recoverable Fe₃O₄-modified ternary CoFeCu-layered double hydroxides (Fe₃O₄/CoFeCu-LDHs) was prepared by a simple co-precipitation method and initially applied to activate PMS for the degradation of Rhodamine B (RhB). X-ray diffraction (XRD), fourier transform infrared spectrometer (FT-IR), scanning electron microscope (SEM), transmission electron microscopy (TEM), Brunauer-Emmett-Teller method (BET), and vibrating sample magnetometer (VSM) were applied to characterize morphology, structure, specific surface area and magnetism. In addition, the effects of several key parameters were evaluated. The Fe₃O₄/CoFeCu-LDHs exhibited high catalytic activity, and RhB degradation efficiency could reach 100% within 20 min by adding 0.2 g/L of catalyst and 1 mmol/L of PMS into 50 mg/L of RhB solution under a wide pH condition (3.0-7.0). Notably, the Fe₃O₄/CoFeCu-LDHs showed good super-paramagnetism and excellent stability, which could be effectively and quickly recovered under magnetic condition, and the degradation efficiency after ten cycles could still maintain 98.95%. Both radicals quenching tests and electron spin resonance (ESR) identified both HO? and SO₄^?? were involved and SO₄^?? played a dominant role on the RhB degradation. Finally, the chemical states of the sample's surface elements were measured by X-ray photoelectron spectroscopy (XPS), and the possible activation mechanism in Fe₃O₄/CoFeCu-LDHs/PMS system was proposed according to comprehensive analysis.     

Identification of close relationship between atmospheric oxidation and ozone formation regimes in a photochemically active region

Understanding ozone (O₃) formation regime is a prerequisite in formulating an effective O₃ pollution control strategy. Photochemical indicator is a simple and direct method in identifying O₃ formation regimes. Most used indicators are derived from observations, whereas the role of atmospheric oxidation is not in consideration, which is the core driver of O₃ formation. Thus, it may impact accuracy in signaling O₃ formation regimes. In this study, an advanced three-dimensional numerical modeling system was used to investigate the relationship between atmospheric oxidation and O₃ formation regimes during a long-lasting O₃ exceedance event in September 2017 over the Pearl River Delta (PRD) of China. We discovered a clear relationship between atmospheric oxidative capacity and O₃ formation regime. Over eastern PRD, O₃ formation was mainly in a NO_x-limited regime when HO₂/OH ratio was higher than 11, while in a VOC-limited regime when the ratio was lower than 9.5. Over central and western PRD, an HO₂/OH ratio higher than 5 and lower than 2 was indicative of NO_x-limited and VOC-limited regime, respectively. Physical contribution, including horizontal transport and vertical transport, may pose uncertainties on the indication of O₃ formation regime by HO₂/OH ratio. In comparison with other commonly used photochemical indicators, HO₂/OH ratio had the best performance in differentiating O₃ formation regimes. This study highlighted the necessities in using an atmospheric oxidative capacity-based indicator to infer O₃ formation regime, and underscored the importance of characterizing behaviors of radicals to gain insight in atmospheric processes leading to O₃ pollution over a photochemically active region.     

Numerical simulation of overtopping breach processes caused by failure of landslide dams

Environmental Fluid Mechanics - Based on the mechanism of landslide dam failure caused by overtopping, a simplified mathematical model for simulating dam breach overtopping flow processes was...