氮肥水平对不同土壤CH4排放的影响

鉴于氮肥施用对农田CH₄排放的影响还有很大不确定性,室外盆栽试验于2002年在南京农业大学实施.选取3个供试土壤,各土壤设置对照和低、中、高3个不同氮肥水平,施入尿素量分别为0 g/盆钵(对照) ,0.64g/盆钵,(低氮水平) ,1.28g/盆钵(中氮水平) ,1.93g/盆钵(高氮水平) .结果表明在水稻生长季,不同氮肥(尿素)施用量对稻田土壤CH₄排放影响表现为不同土壤之间,及不同氮肥水平之间CH₄排放均存在显著差异.无氮肥施入的情况下,3种土壤的CH₄季节性累积排放量存在显著差异,分别为6.7g/m²,12.6g/m² 和8.3g/m².施加氮肥后,3种土壤的CH4排放量随氮肥施入量的增加,均表现为降低趋势,不同土壤CH₄排放量存在差异,土壤背景氮含量最高的F(江苏溧水)土壤的CH4排放都比相应氮肥水平下的G(江苏涟水)和H(江苏农科院)土壤的CH₄排放低1倍左右.更进一步发现从低氮到中氮水平,3种土壤CH₄排放量随氮肥用量的增加降低幅度最大,而此时各土壤的NH₄-N含量随氮肥用量增加明显提高,推断造成CH₄排放降低的主要可能原因是各土壤的氨态氮含量的增加所致.从中氮到高氮水平3种土壤的CH₄排放量的变化不尽相同,G和H土壤的CH₄排放量随氮肥用量的增加而降低,而F土壤在中氮和高氮水平下的CH4排放量没有明显变化,值分别为30g/m².     

北京市大气PM2.5中矿物成分的污染特征

为了解北京市大气细粒子中矿物成分的浓度水平和污染特征,在清华园和车公庄进行了连续1a的PM_2.5累积周采样和全样品分析.Al、Si、Ca、Mg和Fe等地壳元素的周变化相似,最大周均浓度均出现在春季有强沙尘天气的一周;其季节变化显著,显示季节性的源排放以及气象条件对矿物成分的含量影响显著.土壤尘的季节平均浓度从夏季逐步上升,至次年春季达到最高(21.1 μg·m^-3),表明春季频繁发生的沙尘天气对土壤尘细粒子有重要贡献.大量的建筑活动可能大大增加了北京细粒子中Ca的负荷,应加强其排放控制.     

中国西部本底大气中CO的连续测量

在中国西北部的瓦里关全球基准站(36°17'N,100°54'E,3810m asl)建立了气相色谱-汞置换法大气CO连续测量系统.组装调试和运行标定表明,色谱方法的基线稳定,分离度高,检测方法可靠,系统具有高自动化的操作性能和严格的质量控制,其设计完全符合世界气象组织(WMO)全球大气本底测量的要求.根据采样现场大气CO浓度的变化,采用经国际比对的CO标准气系列,用峰高外标法设定可调整的标准工作曲线计算环境CO浓度,系统对CO的检测限低至1×10^-9(V/V),检测精度小于0.1%,准确度在±0.05%以内,可提供我国本底地区近地层大气CO连续而精确的现场测量结果.     

种植密度和降水对冬小麦田N2O排放的影响

为研究种植密度对农田N2O排放的影响和探讨N₂O排放季节性波动的原因,于1999～2000年小麦生长季在南京市郊江宁县进行了不同播种量(0、90、180和270kg/hm²)的大田试验.观测分析结果表明:在相同的气象条件和田间管理下,播种～越冬阶段的N₂O排放不受播种量的影响,返青～成熟阶段的N₂O排放通量与播种量成正比.裸地条件下的N₂O排放与播量为90kg/hm²下的排放无明显差异.造成该生长季内N₂O排放季节性波动的主要原因是降水,返青～成熟阶段的N₂O排放通量随观测日前6d的加权平均降水量呈指数增加.     

短期干旱胁迫对马尾松排放挥发性有机物的影响

为探究干旱环境对BVOCs排放的影响,应用动态封闭式采样系统和热脱附-气相色谱-飞行质谱仪,对短期干旱胁迫作用下马尾松的BVOCs排放进行了实验室测量,定量分析BVOCs排放速率和排放组成的变化.结果表明,干旱胁迫时异戊二烯的排放受到抑制,排放速率降低约50%;单萜烯和倍半萜烯的排放水平增强,排放速率分别为137.85和0.98μg/（m²·h）,是未受胁迫时的2.9和2.0倍.除反式-α-香柠檬烯外,干旱胁迫促进各单萜烯和倍半萜烯化合物的排放,是未受胁迫时的1.3~42.4倍,其中3-蒈烯排放的响应最敏感,α-葑烯、α-水芹烯和石竹烯的响应最弱.干旱胁迫时单萜烯和倍半萜烯的排放组成有所变化,但主导的化合物种类不变,单萜烯以α-蒎烯、香桧烯和β-蒎烯为主,占比分别为48%、17%和17%;倍半萜烯以石竹烯和长叶烯为主,占比分别为57%和34%.     

Characterization of atmospheric aerosol (PM10 and PM2.5) from a medium sized city in São Paulo state, Brazil

Air pollution causes deleterious effects on human health with aerosols being among the most polluting agents.The objective of this work is the characterization of the PM_(2.5) and PM_(10) aerosol mass in the atmosphere.The methods of analysis include WD-XRF and EDS.Data were correlated with meteorological information and air mass trajectories(model HYSPLIT)by multivariate analysis.A morphological structural analysis was also carried out to identify the probable sources of atmospheric aerosols in the city of Sao Jose do Rio Preto,Brazil.The mean mass concentration values obtained were 24.54 μg/m~3 for PM_(10),above the WHO annual standard value of 20 μg/m~3 and 10.88 μg/m~3 for PM_(2.5) whose WHO recommended limit is10 μg/m~3.WD-XRF analysis of the samples revealed Si and Al as major components of the coarse fraction.In the fine fraction,the major elements were Al and S.The SEM-FEG characterization allowed identifying the morphology of the particles in agglomerates,ellipsoids and filaments in the PM_(10),besides spherical in the PM_(2.5).The analysis by EDS corroborated WD-XRF results,identifying the crustal elements,aluminosilicates and elements of anthropogenic origin in the coarse fraction.For the fine fraction crustal elements were also identified;aluminosilicates,black carbon and spherical particles(C and O) originating from combustion processes were predominant.The use of multivariate analysis to correlate air mass trajectories with the results of the morpho-structural characterization of the particulate matter allowed confirmation of the complex composition of the particles resulting from the combination of both local and long-distance sources.     

Treatability studies of naphthalene in soil,water and air with persulfate activated by iron(Ⅱ)

Chemical oxidation was applied to an artificially contaminated soil with naphthalene (NAP). Evaluation of NAP distribution and mass reduction in soil, water and air phases was carried out through mass balance. Evaluation of NAP distribution and mass reduction in soil, water and air phases was carried out through mass balance. The importance of the air phase analysis was emphasized by demonstrating how NAP behaves in a sealed system over a 4 hr reaction period. Design of Experiments method was applied to the following variables: sodium persulfate concentration [SP], ferrous sulfate concentration [FeSO₄], and pH. The system operated with a prefixed solid to liquid ratio of 1:2. The following conditions resulted in optimum NAP removal [SP] = 18.37 g/L, [FeSO₄] = 4.25 g/L and pH = 3.00. At the end of the 4 hr reaction, 62% of NAP was degraded. In the soil phase, the chemical oxidation reduced the NAP concentration thus achieving levels which comply with Brazilian and USA environmental legislations. Besides the NAP partitioning view, the monitoring of each phase allowed the variabilities assessment over the process, refining the knowledge of mass reduction. Based on NAP distribution in the system, this study demonstrates the importance of evaluating the presence of semi-volatile and volatile organic compounds in the air phase during remediation, so that there is greater control of the system as to the distribution and presence of the contaminant in the environment. The results highlight the importance of treating the contaminant in all its phases at the contaminated site.     

Effect of substituents in hydroxyl radical-mediated degradation of azo pyridone dyes: Theoretical approaches on the reaction mechanism

Understanding the degradation behavior of azo dyes in photocatalytic wastewater treatment is of fundamental and practical importance for their application in textile-processing and other coloration industries. In this study, quantum chemistry, as density functional theory, was used to elucidate different degradation pathways of azo pyridone dyes in a hydroxyl radical (HO^?)-initiated photocatalytic system. A series of substituted azo pyridone dyes were synthesized by changing the substituent group in the para position of the benzene moiety, ranging from strong electron-donating to strong electron-withdrawing groups. The effect of dye molecular structure on the photocatalytic degradation reaction mechanism was analyzed and quantification of substituent effects on the thermodynamic and kinetics parameters was performed. Potential energy surface analysis revealed the most susceptible reaction site for the HO^? attack. The calculated reaction barriers are found to be strongly affected by the nature of substituent group with a good correlation using Hammett σ_p constants and experimentally determined reaction rates. The stability of pre-reaction complexes and transition state complexes were analyzed applying the distortion-interaction model. The increased stability of the transition state complexes with the distancing from the substituent group has been established.     

Reactive uptake of NO2 on volcanic particles: A possible source of HONO in the atmosphere

The heterogeneous degradation of nitrogen dioxide (NO₂) on five samples of natural Icelandic volcanic particles has been investigated. Laboratory experiments were carried out under simulated atmospheric conditions using a coated wall flow tube (CWFT). The CWFT reactor was coupled to a blue light nitrogen oxides analyzer (NO_x analyzer), and a long path absorption photometer (LOPAP) to monitor in real time the concentrations of NO₂, NO and HONO, respectively. Under dark and ambient relative humidity conditions, the steady state uptake coefficients of NO₂ varied significantly between the volcanic samples probably due to differences in magma composition and morphological variation related with the density of surface OH groups. The irradiation of the surface with simulated sunlight enhanced the uptake coefficients by a factor of three indicating that photo-induced processes on the surface of the dust occur. Furthermore, the product yields of NO and HONO were determined under both dark and simulated sunlight conditions. The relative humidity was found to influence the distribution of gaseous products, promoting the formation of gaseous HONO. A detailed reaction mechanism is proposed that supports our experimental observations. Regarding the atmospheric implications, our results suggest that the NO₂ degradation on volcanic particles and the corresponding formation of HONO is expected to be significant during volcanic dust storms or after a volcanic eruption.     

Bioaccumulation and depuration of chromium in the selected organs and whole body tissues of freshwater fish Cirrhinus mrigala individually and in binary solutions with nickel

Contamination of aquatic ecosystems with heavy metals has been receiving increased worldwide attention due to their harmful e ects on human health and other organisms in the environment. Most of the studies dealing with toxic e ects of metals deal with single metal species, while the aquatic organisms are typically exposed to mixtures of metals. Hence, in order to provide data supporting the usefulness of freshwater fish as indicators of heavy metal pollution, it has been proposed in the present study to investigate the bioaccumulation and depuration of chromium in the selected organs of freshwater fingerlings Cirrhinus mrigala, individually and in binary solutions with nickel. The results show that the kidney is a target organ for chromium accumulation, which implies that it is also the “critical” organ for toxic symptoms. The results further show that accumulation of nickel in all the tissues of C. mrigala is higher than that of chromium. In addition, the metal accumulations of the binary mixtures of chromium and nickel are substantially higher than those of the individual metals, indicating synergistic interactions between the two metals. Theoretically the simplest explanation for an additive joint action of toxicants in a mixture is that they act in a qualitatively similar way. The observed data suggest that C. mrigala could be suitable monitoring organisms to study the bioavailability of water-bound metals in freshwater habitats.