通过屋顶暴露方法模拟聚碳酸酯微塑料在长江水样的长期老化行为

由于较低的自然老化速率,微塑料在实际水体长期户外暴露过程中老化行为的数据仍较缺乏.通过聚碳酸酯（Polycarbonate,PC）微塑料在长江表层水样的18个月户外暴露试验以揭示自然老化过程对微塑料表面特征及对金属离子(Cr⁶⁺和Co²⁺)吸附行为的重要影响.结果显示,户外暴露改变了PC微塑料的理化性质,包括表面开裂、粒径降低、亲水性和熔点增加以及表面氧化（产生羰基和羟基）.同时,户外老化过程明显影响微塑料对金属离子的吸附行为.原始和低老化程度PC对金属离子的吸附主要通过物理作用控制,而高老化程度微塑料由于产生含氧功能团对金属离子的吸附主要由化学过程如络合和共价键等作用控制.并且,不同老化程度PC微塑料对Cr⁶⁺和Co²⁺的吸附性能不同.对于Cr⁶⁺,PC的吸附性能随其老化程度增加呈先升高后降低的趋势,然而对于Co²⁺,平衡吸附性能随老化程度增加呈增加的趋势.户外老化过程产生含氧官能团、破碎和开裂以及生物膜可能是影响吸附性能的主要因素.本研究证实了长期户外...     

农业土地利用转变对土壤团聚体组成及碳、氮含量的影响

为探究农业土地利用转变对土壤团聚体组成、稳定性及有机碳（SOC）、全氮（TN）含量变化的影响,选取玉米地、玉米地转变为姜地、稻田和稻田转变为姜地4种农业土地利用类型为研究对象,对土壤水稳性团聚体的组成、稳定性及SOC、TN含量进行测定与分析.结果表明： ①玉米地转变为姜地后,>0.25 mm粒级的大团聚体减少21.48%（p<0.01）,>0.25 mm稳定性团聚体的含量（DR_0.25）显著降低53.39%;稻田转变为姜地后,大团聚体差异不显著,<0.053 mm粒级的粉黏团聚体增加8.93%（p<0.01）;冗余分析和相关分析表明,土壤含水量是团聚体组成和 稳定性的重要影响因素;②玉米地转变为姜地后,0.25~1 mm粒级团聚体中SOC、TN含量分别减少52.68%、50.98%,粉黏团聚体（<0.053 mm）中SOC和TN含量增加约2倍（p<0.01）;稻田转变为姜地后,>0.25 mm的大团聚体和0.053~0.25 mm的微团聚体中的SOC、TN含量均减少（p<0.05）,其中,大团聚体碳氮比与团聚体组成和稳定性存在相关关系（p<0.05）;③所有处理均为大团聚体SOC、TN贡献率最高,转变后的姜地较玉米地、稻田的土壤粉黏团聚体的SOC、TN贡献率显著增加,尤其是较玉米地的粉黏团聚体SOC、TN贡献率增加3倍（p<0.01）;④平均质量 直径（MWD）和几何平均直径（GMD）与大团聚体的SOC、TN含量呈显著正相关（p<0.05）,分形维数（D）与MWD及1~2 mm粒级大团聚体的SOC、TN含量呈显著负相关（p<0.01）,DR_0.25与大团聚体的SOC、TN含量呈显著正相关（p<0.01）.总体上,玉米地和稻田两种用地转变为姜地后,土壤团聚体的组成发生较大变化,团聚体稳定性变化虽不显著,但大团聚体中SOC、TN含量降低,粉黏团聚体中SOC、TN含量增加.本研究的开展对农田科学管理和可持续生产具有重要的指导意义.     

中国冰雪资源高质量开发：理论审视、实践转向与挑战应对

推动冰雪资源高质量开发,是实现联合国可持续发展目标的新路径与新模式,是践行“两山理论”的重要环节,也是落实全民健身国家战略、助力体育强国建设的重要手段。在实际建设的理论指导层面,社会学所倡导的幸福感理论明确了冰雪资源高质量开发的终极目标,资源经济学的资源价值理论为冰雪资源的价值认识及价格核算提供了科学工具,地理学的人地关系理论是探究空间分异规律及人地系统耦合路径的理论基石。基于我国冰雪资源开发实践的系列转变及现实挑战,提出我国冰雪资源高质量开发的实现路径,即坚持观念创新的发展方式、多重协调的发展要求、积极开放的发展理念以及主客共赢的发展目标。     

基于无人机影像的城市植被精细分类

针对传统植被资源调查方法工作量大、成本高、效率低的问题,利用高分辨率无人机遥感影像,联合地物光谱-纹理-空间信息,构建了一种适用于描述城市不同植被种类的多维特征空间,在此基础上对三种应用广泛的分类算法(基于像素的、面向对象的支持向量机及深度学习Mobile-Unet语义分割模型)开展了对比分析研究.结果表明:本文提出的联合地物光谱-纹理-空间信息的特征空间构建方法能够有效地描述城市不同类型植被的特征差异,提升影像分割、植被分类的精度;在分类精度上,基于像素和面向对象的支持向量机分类结果的总体精度均超过90%,深度学习方法的总体分类精度为84%;在算法效率上,传统机器学习方法也优于深度学习方法.因此,得出结论针对城市小区域、小样本的植被精细分类,传统机器学习分类方法比深度学习方法效果更好.     

基于RuO2-IrO2/Ti和Fe0电极的电氧化-电絮凝处理含Tl废水

基于RuO₂-IrO₂/Ti形稳电极和Fe⁰牺牲电极实现电氧化-电絮凝(EO-EC)一体化处理含Tl (I)废水,并与单一的电絮凝(EC)进行比较,探讨了EO-EC处理含Tl废水的机理.结果表明,相较于单一EC,EO-EC (1:1)组合技术适应于宽pH (4-10)以及电流密度范围(5-20mA/cm²)下含Tl废水高效处理,且不易发生钝化;活性氯以及氧化还原电位在Tl (I)间接氧化Tl (III)过程中扮演重要角色,沉淀分析表明生成的Tl (OH)_3(s)与絮体Fe (OH)_3(am)共沉淀,纤铁矿位点可吸附残留Tl (I).EO-EC一体化技术可满足实际含Tl废水达标处理(<2µg/L)且具有经济可行性.     

未来RCP4.5情景下黄海DMS浓度变化模拟与分析

使用CORDEX-EA过去气候态(2000-2009年)与RCP4.5情景下近未来气候态(2041-2050年)大气强迫结果驱动中国东部陆架海域耦合DMS模块生态模型,模拟了黄海过去及近未来表层DMS浓度(C_DMS),探究了黄海近未来C_DMS时空分布的变化及其影响因素.结果表明:近未来黄海C_DMS的年循环发生变化,北黄海C_DMS极高值出现月份由5、9月转变为4、10月,南黄海由4、9月转变为4、8月;局部C_DMS高值区也发生变化,春季山东半岛附近海域、夏季苏北浅滩、南黄海中东部、秋季南黄海东部C_DMS高值区加强,夏季山东半岛附近C_DMS高值区减弱.近未来热通量、风应力对山东半岛、南黄海中东部海域C_DMS影响较大;降水量、云量对西朝鲜湾C_DMS的影响占优;苏北浅滩C_DMS受多个气候因子共同作用.     

Extracellular polymeric substance induces biogenesis of vivianite under inorganic phosphate-free conditions

Vivianite is often found in reducing environments rich in iron and phosphorus from organic debris degradation or phosphorus mineral dissolution. The formation of vivianite is essential to the geochemical cycling of phosphorus and iron elements in natural environments. In this study, extracellular polymeric substances (EPS) were selected as the source of phosphorus. Microcosm experiments were conducted to test the evolution of mineralogy during the reduction of polyferric sulfate flocs (PFS) by Shewanella oneidensis MR-1 (S. oneidensis MR-1) at EPS concentrations of 0, 0.03, and 0.3 g/L. Vivianite was found to be the secondary mineral in EPS treatment when there was no phosphate in the media. The EPS DNA served as the phosphorus source and DNA-supplied phosphate could induce the formation of vivianite. EPS impedes PFS aggregation, contains redox proteins and stores electron shuttle, and thus greatly promotes the formation of minerals and enhances the reduction of Fe(III). At EPS concentration of 0, 0.03, and 0.3 g/L, the produced HCl-extractable Fe(II) was 107.9, 111.0, and 115.2 mg/L, respectively. However, when the microcosms remained unstirred, vivianite can be formed without the addition of EPS. In unstirred systems, the EPS secreted by S. oneidensis MR-1 could agglomerate at some areas, resulting in the formation of vivianite in the proximity of microbial cells. It was found that vivianite can be generated biogenetically by S. oneidensis MR-1 strain and EPS may play a key role in iron reduction and concentrating phosphorus in the oligotrophic ecosystems where quiescent conditions prevail.     

Identification and characterization of Fe3O4/peroxodisulfate advanced oxidation products from sulfameter

Sulfonamides (SAs) are one of the most widely used antibiotics and their residuals in the environment could cause some negative environmental issues. Advanced oxidation such as Fenton-like reaction has been widely applied in the treatment of SAs polluted water. Degradation rates of 95%-99.7% were achieved in this work for the tested 8 SAs, including sulfisomidine, sulfameter (SME), phthalylsulfathiazole, sulfamethoxypyridazine, sulfamonomethoxine, sulfisoxazole, sulfachloropyridazine, and sulfadimethoxine, in the Fe₃O₄/peroxodisulfate (PDS) oxidation system after the optimization of PDS concentration and pH. Meanwhile, it was found that a lot of unknown oxidation products were formed, which brought up the uncertainty of health risks to the environment, and the identification of these unknown products was critical. Therefore, SME was selected as the model compound, from which the oxidation products were never elucidated, to identify these intermediates/products. With liquid chromatography-high resolution tandem mass spectrometry (LC-HRMS/MS), 10 new products were identified, in which 2-amino-5-methoxypyrimidine (AMP) was confirmed by its standard. The investigation of the oxidation process of SME indicated that most of the products were not stable and the degradation pathways were very complicated as multiple reactions, such as oxidation of the amino group, SO₂ extrusion, and potential cross-reaction occurred simultaneously. Though most of the products were not verified due to the lack of standards, our results could be helpful in the evaluation of the treatment performance of SAs containing wastewater.     

Year-round observation of atmospheric inorganic aerosols in urban Beijing: Size distribution, source analysis, and reduction mechanism

To investigate particle characteristics and find an effective measure to control severe particle pollution, year-round observation of size-segregated inorganic aerosols was conducted in Beijing from January to December, 2016. The sampled atmospheric particles all presented bimodal size distribution at four pollution levels (clear, slight pollution, moderate pollution and severe pollution), and peak values appeared at the size range of 0.7-2.1 μm and >9.0 μm, respectively. As dominant particle compositions, NO₃⁻, SO₄²⁻, and NH₄⁺ in four pollution levels all showed significant peaks in fine mode, especially at the size range of 1.1-2.1 μm. Secondary inorganic aerosols accounted for about 67.6% (36.3% (secondary sulfates) + 31.3% (secondary nitrates)) of the total sources of fine particles in urban Beijing. Severe pollution of fine particles was mainly caused by the air masses transported from nearby western and southern areas, which are industrial and densely populated region, respectively. Sensitivity tests further revealed that the control measures focusing on ammonium emission reduction was the most effective for particle pollution mitigation, and fine particles all showed nonlinear responses after reducing ammonium, nitrate, and sulfate concentrations, with the fitting curves of y = -120.8x - 306.1x² + 290.2x³, y = -43.5x - 67.8x², and y = -25.8x - 110.4x² + 7.6x³, respectively (y and x present fine particle mass variation (μg/m³) and concentration reduction ratio (CRR)/100 (dimensionless)). Overall, our study presents useful information for understanding the characteristics of atmospheric inorganic aerosols in urban Beijing, as well as offers policy makers with effective measure for mitigating particle pollution.     

功能化材料Zr@AC对水中难降解农药阿特拉津的去除特征

我国农药阿特拉津的污染十分严重,对生态系统造成了非常不利的影响. 为了实现对水环境中阿特拉津的高效去除和吸附剂的重复利用,该研究通过溶液浸渍和高温煅烧技术将金属锆负载到活性炭上,制备出功能化材料Zr@AC,使用扫描电镜(SEM)、X射线衍射仪(XRD)、傅里叶变换红外吸收光谱仪(FTIR)和比表面及孔径分析仪(BET)对材料的形貌和组成进行了表征,并考察了Zr@AC对水中阿特拉津的去除效果. 结果表明:①当浸渍液锆离子的质量分数为7.0%、浸渍时间为9.0 h、煅烧温度为500 ℃和煅烧时间为5.0 h时,制备的Zr@AC具有较大的比表面积、较多的中孔和微孔以及丰富的活性位点. ②对阿特拉津的去除研究表明,当溶液pH为4.0、温度为25 ℃、Zr@AC投加量为60.0 mg/L时,经过90 min的反应,Zr@AC对阿特拉津的吸附容量最大,达到93.8 mg/g. ③动力学模拟研究表明,该吸附过程遵循拟二级动力学模型,且Freundlich等温吸附模型的拟合结果要优于Langmuir等温吸附模型,说明Zr@AC对阿特拉津的吸附存在化学吸附和多分子层吸附的双重作用. ④经过5次重复试验后,Zr@AC对阿特拉津的去除率仍有83.9%. 研究显示,Zr@AC可作为水中去除阿特拉津的吸附剂,是一种很有前途、可重复多次使用的材料.