长三角绿色技术创新网络结构特征与优化策略

绿色技术创新作为区域技术创新体系的重要组成部分,是维持区域发展可持续性、增强区域竞争优势的重要驱动力.基于区域一体化的研究视角,通过采集长三角绿色技术专利合作及绿色技术转移数据,运用Gephi复杂网络分析方法,对长三角绿色技术创新网络进行结构分析.结果 表明:(1)长三角绿色技术创新网络发育程度较低,大量城市在绿色技术创新网络中较边缘化;(2)绿色技术创新依赖创新主体间知识互动,地理邻近促进了创新合作行为的产生和知识的扩散;(3)长三角绿色技术创新网络"强-强联系"与"核心-边缘"结构特征明显,绿色技术专利合作网络呈现"一超多强"的多中心格局,绿色技术转让网络呈现单中心格局;(4)区域一体化下,长三角绿色技术创新网络兼具邻近性和等级性特征,不同类型城市参与创新网络应有差异;进而,提出长三角绿色技术创新网络优化策略.创新点在于:建立了区域一体化与技术创新网络的关联,探讨了绿色技术创新的空间组织形式,强调了地理邻近对于绿色技术创新网络的重要性.     

试论生态文明制度体系的构建

建立健全生态文明制度体系是推进我国生态文明建设的重点。党的十八届三中全会通过的《中共中央关于全面深化改革若干重大问题的决定》指出,生态文明制度体系应当包括决策制度、评价制度、管理制度与考核制度等内容。立足社会主义制度建设的中国特色,针对我国生态文明建设的具体需求,本文将生态文明制度体系解构为四大板块:绿色高效决策制度、生态有价评估制度、生态环境监管制度与生态优先考核制度,并进一步明确了各项制度构建工作的具体内容。生态文明制度体系的构建和不断完善,将为全面建成人与自然和谐的美丽中国提供系统保障。     

Evaluation of photolysis and hydrolysis of pyraclostrobin in aqueous solutions and its degradation products in paddy water

This study evaluated the hydrolysis and photolysis kinetics of pyraclostrobin in an aqueous solution using ultra-high-performance liquid chromatography–photodiode array detection and identified the resulting metabolites of pyraclostrobin by hydrolysis and photolysis in paddy water using high-resolution mass spectrometry coupled with liquid chromatography. The effect of solution pH, metal ions and surfactants on the hydrolysis of pyraclostrobin was explored. The hydrolysis half-lives of pyraclostrobin were 23.1–115.5?days and were stable in buffer solution at pH 5.0. The degradation rate of pyraclostrobin in an aqueous solution under sunlight was slower than that under UV photolysis reaction. The half-lives of pyraclostrobin in a buffer solution at pH 5.0, 7.0, 9.0 and in paddy water were less than 12?h under the two light irradiation types. The metabolites of the two processes were identified and compared to further understand the mechanisms underlying hydrolysis and photolysis of pyraclostrobin in natural water. The extracted ions obtained from paddy water were automatically annotated by Compound Discoverer software with manual confirmation of their fragments. Two metabolites were detected and identified in the pyraclostrobin hydrolysis, whereas three metabolites were detected and identified in the photolysis in paddy water.     

Determination of the residue dynamics and dietary risk of thiamethoxam and its metabolite clothianidin in citrus and soil by LC-MS/MS

A modified quick, easy, cheap, effective, rugged and safe (QuEChERS) method was developed for the determination of thiamethoxam and its metabolite clothianidin in citrus (including the whole citrus, peel and pulp) and soil samples by liquid chromatography-tandem mass spectrometry. The sample was extracted with acetonitrile and purified with octadecylsilane. The detection limits of both compounds were 0.0001–0.0002?mg kg^–1, while the limit of quantification of thiamethoxam was 0.002?mg kg^–1 and the limit of quantitation of metabolites was 0.001?mg kg^–1. The recovery was 70.37%–109.76%, with inter-day relative standard deviations (RSD) (n?=?15) values ≤9.46% for the two compounds in the four matrices. The degradation curve of thiamethoxam in whole citrus and soil was plotted using the first-order kinetic model. The half-life of the whole citrus was 1.9–6.2?days, and the half-life of the soil was 3.9–4.2?days. The terminal residue of thiamethoxam (the sum of thiamethoxam and clothianidin, expressed as thiamethoxam) was found to be concentrated on the peel. The final residual amount of thiamethoxam in the edible portion (pulp) was less than 0.061?mg kg^–1. The risk quotient values were all below 1, indicating that thiamethoxam as a citrus insecticide does not pose a health risk to humans at the recommended dosage.     

The regulatory role of endogenous iron on greenhouse gas emissions under intensive nitrogen fertilization in subtropical soils of China

Environmental Science and Pollution Research - Anaerobic batch experiments were conducted to study the regulatory role of endogenous iron in greenhouse gas emissions under intensive nitrogen...     

Fungicidal values of bio-oils and their lignin-rich fractions obtained from wood/bark fast pyrolysis

Pine wood, pine bark, oak wood and oak bark were pyrolyzed in an auger reactor. A total of 16 bio-oils or pyrolytic oils were generated at different temperatures and residence times. Two additional pine bio-oils were produced at the National Renewable Energy Laboratory in a fluidized-bed reactor at different temperatures. All these bio-oils were fractionated to obtain lignin-rich fractions which consist mainly of phenols and neutrals. The pyrolytic lignin-rich fractions were obtained by liquid-liquid extraction. Whole bio-oils and their lignin-rich fractions were studied as potential environmentally benign wood preservatives to replace metal-based CCA and copper systems that have raised environmental concerns. Each bio-oil and several lignin-rich fractions were tested for antifungal properties. Soil block tests were conducted using one brown-rot fungus (Gloeophyllum trabeum) and one white-rot fungus (Trametes versicolor). The lignin-rich fractions showed greater fungal inhibition than whole bio-oils for a impregnation solution 10% concentration level. Water repellence tests were also performed to study wood wafer swelling behavior before and after bio-oil and lignin-rich fraction treatments. In this case, bio-oil fractions did not exhibit higher water repellency than whole bio-oils. Comparison of raw bio-oils in soil block tests, with unleached wafers, at 10% and 25% bio-oil impregnation solution concentration levels showed excellent wood preservation properties at the 25% level. The good performance of raw bio-oils at higher loading levels suggests that fractionation to generate lignin-rich fractions is unnecessary. At this more effective 25% loading level in general, the raw bio-oils performed similarly. Prevention of leaching is critically important for both raw bio-oils and their fractions to provide decay resistance. Initial tests of a polymerization chemical to prevent leaching showed some success.     

Distribution of elements in needles of Pinus massoniana (Lamb.) was uneven and affected by needle age

Macronutrients (P, S, K, Na, Mg, Ca), heavy metals (Fe, Zn, Mn, Cu, Pb, Cr, Ni, Cd,) and Al concentrations as well as values of Ca/Al in the tip, middle and base sections, and sheaths of current year and previous year needles of Pinus massoniana from Xiqiao Mountain were analyzed and the distribution patterns of those elements were compared. The results indicated that many elements were unevenly distributed among the different components of needles. Possible deficiency of P, K, Ca, Mn and Al toxicity occurred in needles under air pollution. Heavy metals may threaten the health of Masson pine. Needle sheaths were good places to look for particulate pollutants, in this case including Fe, Cu, Zn, Pb, Cr, Cd and Al.     

长江河口近岸水体自然净化作用及其初步评价

按照水体的净化机理，结合长江口和上海滨岸带近岸水体的物理、化学和生物等因素的实际特征，对近岸水体的自然净化作用进行了阐述和分析。并在历史资料和实测资料基础上，就近岸水体的自然净化作用进行了评价。评价结果表明，因长江河口近岸水体存在较强的自然净化作用机制，近岸水体体的自然净化能力较强，环境容量较大，但由于污染物输入量的不断增加，部分岸段近岸水体的环境质量有逐渐下降的趋势；近岸水体的自然净化作用具有明显的季节性变化，长江口南岸水域洪水季节水体的自然净化作用比估水季节强，而杭州湾北岸水域的自然净化作用表现为相反的变化趋势，因此建议在近岸污水排放过程中应考虑近岸水体的净化能力，遵循水体的自然净化作用规律。     

典型西南工业城市柳州市核心区大气污染物时空分布与气象因素研究

为研究柳州市核心区大气污染物浓度时空变化规律与气象因素之间的关系,统计分析了2018年全年研究区内6个自动监测站点PM_(2.5)、PM_(10)、SO_2、NO_2、O_3和CO的浓度监测数据和气象站气象数据,并对28次超标日污染物来源进行了解析.结果显示:①核心区颗粒污染物污染较为严重,且以PM_(2.5)为主的细颗粒污染物仍为柳州市主要的大气污染物;各污染物月均浓度季节差异显著,除NO_2外柳州大气污染物浓度下降明显,指示柳州市多项节能减排综合整治措施成效显著;PM_(2.5)、PM_(10)、CO受早晚高峰期影响,浓度日变化均呈双峰型;NO_2在不同季节峰型不同,作为O_3前体物其浓度日变化与O_3相反,呈现"早峰午谷"的变化趋势.②通过对污染物浓度插值发现,由于核心区主要工商业区位于西部且处于主导风向下风向,故PM_(2.5)和SO_2浓度西北高、东南低,PM_(10)、NO_2和CO浓度西南高、东北低;核心区东部的山区为O_3生成带来大量前体物,使O_3浓度东南高、西北低.③由于气候特征,核心区春、夏季主要气象因素均为降水量;秋季的主要气象因素是风速,风速与污染物的负相关关系表明了风的扩散效应;冬季大部分污染物与气象因素的相关性不显著,表明人为因素对污染物的影响大于气象因素;核心区大气污染物主要来源于局地排放和区域传输,且南北主导风向对大气污染影响最大.④HYSPLIT模型结果指示柳州超标日大气污染物主要来自于珠三角地区,且陆源颗粒物浓度普遍比海洋源高,来自南部的远距离输送气流颗粒物含量最低,表明远距离输送为影响颗粒物传播的主要原因.