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131.
Monitoring the dynamics of vegetation growth and its response to climate change is important to understand the mechanisms underlying ecosystem behaviors. This study investigated the relationship between vegetation growth and climate change during the growing seasons on the Loess Plateau in China by analyzing the normalized difference vegetation index (NDVI) derived from the Land Long Term Data Record dataset from 1982 to 2011. Results showed that growing-season NDVI had increased at an annual rate of 0.0028, particularly in the semi-arid and semi-humid regions. By contrast, the NDVI first increased from 1982 to 1994 (0.0013 year?1, P < 0.05) and then decreased from 1994 to 2011 (0.0016 year?1, P < 0.05) in the arid region. Temperature had a positive effect on NDVI in most periods within and across seasons in the semi-humid region but had no significant effect in the arid region. Precipitation had a positive effect on NDVI in the arid region in summer and in the semi-arid region in autumn. Summer precipitation was important for autumn vegetation growth in the arid region, whereas summer temperature increased autumn vegetation growth in the semi-arid and semi-humid regions. Further analyses supported the lag-time effects of climate change on vegetation growth on the Loess Plateau. Precipitation shifts had 15- to 18-month time lag effects on vegetation growth in the three climate regions. Vegetation NDVI had a 17-month lag response to temperature in the semi-arid region. Human activities should not be neglected in analyzing the relationship between vegetation growth and climate change on the Loess Plateau.  相似文献   
132.
Nonferrous metal is an important basis material for the development of the national economy, and its consumption directly affects economic development. It has great significance in the effective utilization of nonferrous metals, development of an environment-friendly society, and investigation of the decoupling of nonferrous metal consumption and GDP growth. The decoupling indicators for nonferrous metal consumption and GDP growth (D r) in China from 1995 to 2010 were calculated in this study, and the results were analyzed. A productive model based on BP neural network was established. Then, the decoupling indicators for nonferrous metal consumption and GDP growth in China for the period of 2011–2020 were predicted. For the period of 1995–2010, the annual average decoupling indicators were <1 for copper, aluminum, zinc, lead, and nickel, except for tin, which was 0.21. The analysis showed that the decoupling of nonferrous metal consumption and GDP growth is in a less optimistic situation to copper, aluminum, zinc, lead, and nickel in China from 1995 to 2010. The annual average decoupling indicator for tin was 0.21, which indicates relative decoupling. For the period of 2011–2020, the predicted decoupling indicators for copper, aluminum, zinc, lead, nickel, and tin were between 0 and 1. This finding indicates the implementation of relative decoupling. However, the total consumption of nonferrous metals did not decouple from GDP growth.  相似文献   
133.
表面活性剂对多壁碳纳米管吸附Pb~(2+)的影响   总被引:1,自引:0,他引:1  
多壁碳纳米管(MWNT)在吸附有毒气体和重金属离子方面具有极高的应用价值.针对MWNT对水溶液中Pb2+的净化吸附进行了研究,从吸附量,吸附速率、动力学角度考察了表面活性剂、Pb2+浓度对MWNT吸附Pb2+的影响.结果表明,司班-60、吐温-20、阿拉伯树胶等表面活性剂的加入,促进了MWNT在溶液中的分散,导致在Pb2+摩尔浓度为3~18 mmol/L的Lang-muir和Freundlich等温吸附方程中的吸附常数(K)变大,使得MWNT对Pb2+的吸附速率和平衡吸附量都得到提高;随着溶液中Pb2+浓度的增大,MWNT对其吸附量渐至饱和,随后由于Pb2+的位阻作用.吸附量下降;在这3种表面活性剂中,由于司班-60具有相对较小的分子量,其分散的MWNT在Pb2+摩尔浓度为14 mmol/L时,吸附量最大,为230 mg/g.  相似文献   
134.
Spatial gradients of vehicular emitted air pollutants were measured in the vicinity of three roadways in the Austin, Texas area: (1) State Highway 71 (SH-71), a heavily traveled arterial highway dominated by passenger vehicles; (2) Interstate 35 (I-35), a limited access highway north of Austin in Georgetown; and (3) Farm to Market Road 973 (FM-973), a heavily traveled surface roadway with significant truck traffic. A mobile monitoring platform was used to characterize the gradients of CO and NOx concentrations with increased distance from each roadway, while concentrations of carbonyls in the gas-phase and fine particulate matter mass and composition were measured at stationary sites upwind and at one (I-35 and FM-973) or two (SH-71) downwind sites. Regardless of roadway type or wind direction, concentrations of carbon monoxide (CO), nitric oxide (NO), and oxides of nitrogen (NOx) returned to background levels within a few hundred meters of the roadway. Under perpendicular wind conditions, CO, NO and NOx concentrations decreased exponentially with increasing distance perpendicular to the roadways. The decay rate for NO was more than a factor of two greater than for CO, and it comprised a larger fraction of NOx closer to the roadways than further downwind suggesting the potential significance of near roadway chemical processing as well as atmospheric dilution. Concentrations of most carbonyl species decreased with distance downwind of SH-71. However, concentrations of acetaldehyde and acrolein increased farther downwind of SH-71, suggesting chemical generation from the oxidation of primary vehicular emissions. The behavior of particle-bound organic species was complex and further investigation of the size-segregated chemical composition of particulate matter (PM) at increasing downwind distances from roadways is warranted. Fine particulate matter (PM2.5) mass concentrations, polycyclic aromatic hydrocarbons (PAHs), hopanes, and elemental carbon (EC) concentrations generally exhibited concentrations that decreased with distance downwind of SH-71. Concentrations of organic carbon (OC) increased from upwind concentrations immediately downwind of SH-71 and continued to increase further downwind from the roadway. This behavior may have primarily resulted from condensation of semi-volatile organic species emitted from vehicle sources with transport downwind of the roadway.  相似文献   
135.
Measurement of ambient gas-phase total peroxides was performed at the summit of Mount Tai (Mt. Tai, 1534 m above sea level) in central-eastern China during March 22–April 24 and June 16–July 20, 2007. The hourly averaged concentration of peroxides was 0.17 ppbv (± 0.16 ppbv, maximum: 1.28 ppbv) and 0.55 ppbv (± 0.67 ppbv, maximum: 3.55 ppbv) in the spring and summer campaigns, respectively. The average concentration of peroxides at Mt. Tai, which is in a heavily polluted region, was much lower than hydrogen peroxide measurements made at some rural mountain sites, suggesting that significant removal processes took place in this region. An examination of diurnal variation and a correlation analysis suggest that these removal processes could include chemical suppression of peroxide production due to the scavenging of peroxy and hydroxy radicals by high NOx, wet removal by clouds/fogs rich in dissolved sulfur dioxide which reacts quickly with peroxides, and photolysis. These sinks competed with photochemical sources of peroxides, resulting in different mean concentrations and diurnal pattern of peroxides in the spring and summer. A principal component analysis was conducted to quantify the major processes that influenced the variation of peroxide concentrations. This analysis shows that in the spring photochemical production was an important source of peroxides, and the major sink was scavenging during upslope transport of polluted and humid air from the lower part of the planetary boundary layer (PBL) and wet removal by synoptic scale clouds. During the summer, highly polluted PBL air (with high NOx) was often associated with very low peroxides due to the chemical suppression of HO2 by high NOx and wet-removal by clouds/fogs in this sulfur-rich atmosphere, especially during the daytime. Higher concentrations of peroxides, which often appeared at mid-nighttime, were mainly associated with subsidence of air masses containing relatively lower concentrations of NOy.  相似文献   
136.
Vehicular emitted air pollutant concentrations were studied near three types of roadways in Austin, Texas: (1) State Highway 71 (SH-71), a heavily traveled arterial highway dominated by passenger vehicles; (2) Interstate 35 (I-35), a limited access highway north of Austin in Georgetown; and (3) Farm to Market Road 973 (FM-973), a heavily traveled surface roadway dominated by truck traffic. Air pollutants examined include carbon monoxide (CO), oxides of nitrogen (NOx), and carbonyl species in the gas-phase. In the particle phase, ultrafine particle (UFP) concentrations (diameter < 100 nm), fine particulate matter (PM2.5, diameter < 2.5 μm) mass and carbon content and several particle-bound organics were examined. All roadways had an upwind stationary sampling location, one or two fixed downwind sample locations and a mobile monitoring platform that characterized pollutant concentrations fall-off with increased distance from the roadways. Data reported in this paper focus on UFP while other pollutants and near-roadway chemical processes are examined in a companion paper. Traffic volume, especially heavy-duty traffic, wind speed, and proximity to the road were found to be the most important factors determining UFP concentrations near the roadways. Since wind directions were not consistent during the sampling periods, distances along wind trajectories from the roadway to the sampling points were used to study the decay characteristics of UFPs. Under perpendicular wind conditions, for all studied roadway types, particle number concentrations increased dramatically moving from the upwind side to the downwind side. The elevated particle number concentrations decay exponentially with increasing distances from the roadway with sharp concentration gradients observed within 100–150 m, similar to previously reported studies. A single exponential decay curve was found to fit the data collected from all three roadways very well under perpendicular wind conditions. No consistent pattern was observed for UFPs under parallel wind conditions. However, regardless of wind conditions, particle concentrations returned to background levels within a few hundred meters of the roadway. Within measured UFP size ranges, smaller particles (6–25 nm) decayed faster than larger ones (100–300 nm). Similar decay rates were observed among UFP number, surface, and volume.  相似文献   
137.
Using a dynamic numerical atmospheric transport model for organochlorine pesticides (OCPs), the relationship between the East Asian summer monsoon and the fate of α-hexachlorocyclohexane (α-HCH), a banned OCP, in the atmosphere over Northeast Asia was investigated and assessed. The modeled temporal and spatial patterns and variability of α-HCH air concentrations during the summer months of 2005 revealed a strong link between this chemical in the atmosphere over Northeast Asia and the East Asian summer monsoon. At lower atmospheric levels, easterly and southeasterly winds blowing from relatively cold ocean surface convey α-HCH air concentration from southeast China to northeast China. A monsoon front extending from southeast China to Japan, characterized by a strong wind convergence, carried the air concentration to a high elevation of the atmosphere where it was delivered by southerly monsoon flow to northern China and North Pacific Ocean. This summer monsoon associated northward atmospheric transport caused a reversal of the soil/air exchange from outgassing to net deposition during spring–summer period. The modeled wet deposition fluxes of α-HCH agreed well with the changes in the typical summer monsoon rain bands, designated as Meiyu in China, Changma in Korea, and Baiu in Japan. The major wet deposition flux paralleled with the monsoon front as well as the monsoon rain bands. The temporal change in the fluxes exhibits abrupt northward advances, which is associated with a stepwise northward and northeastward advance of the East Asian summer monsoon. The modeled α-HCH outflow in the atmosphere from China occurs mostly in the summer months and through northeast China, featured strongly by the evolution of the summer month. This study suggests that the East Asian summer monsoon provides a major atmospheric pathway and summer outflows to α-HCH over East Asia.  相似文献   
138.
The hydrolysis/precipitation behaviors of Al3+, Al13 and Al30 under conditions typical for flocculation in water treatment were investigated by studying the particulates' size development, charge characteristics, chemical species and speciation transformation of coagulant hydrolysis precipitates. The optimal pH conditions for hydrolysis precipitates formation for AlCl3, PACAl13 and PACAl30 were 6.5–7.5, 8.5–9.5, and 7.5–9.5, respectively. The precipitates' formation rate increased with the increase in dosage, and the relative rates were AlCl3 ? PACAl30 > PACAl13. The precipitates' size increased when the dosage increased from 50 μM to 200 μM, but it decreased when the dosage increased to 800 μM. The Zeta potential of coagulant hydrolysis precipitates decreased with the increase in pH for the three coagulants. The iso-electric points of the freshly formed precipitates for AlCl3, PACAl13 and PACAl30 were 7.3, 9.6 and 9.2, respectively. The Zeta potentials of AlCl3 hydrolysis precipitates were lower than those of PACAl13 and PACAl30 when pH > 5.0. The Zeta potential of PACAl30 hydrolysis precipitates was higher than that of PACAl13 at the acidic side, but lower at the alkaline side. The dosage had no obvious effect on the Zeta potential of hydrolysis precipitates under fixed pH conditions. The increase in Zeta potential with the increase in dosage under uncontrolled pH conditions was due to the pH depression caused by coagulant addition. Al–Ferron research indicated that the hydrolysis precipitates of AlCl3 were composed of amorphous Al(OH)3 precipitates, but those of PACAl13 and PACAl30 were composed of aggregates of Al13 and Al30, respectively. Al3+ was the most un-stable species in coagulants, and its hydrolysis was remarkably influenced by solution pH. Al13 and Al30 species were very stable, and solution pH and aging had little effect on the chemical species of their hydrolysis products. The research method involving coagulant hydrolysis precipitates based on Al–Ferron reaction kinetics was studied in detail. The Al species classification based on complex reaction kinetic of hydrolysis precipitates and Ferron reagent was different from that measured in a conventional coagulant assay using the Al–Ferron method. The chemical composition of Ala, Alb and Alc depended on coagulant and solution pH. The Alb measured in the current case was different from Keggin Al13, and the high Alb content in the AlCl3 hydrolysis precipitates could not used as testimony that most of the Al3+ was converted to highly charged Al13 species during AlCl3 coagulation.  相似文献   
139.
“5·12”汶川地震灾区典型区域生态环境状况影响评价   总被引:2,自引:0,他引:2  
张秋劲  徐亮  周春兰  于飞  刘佳 《四川环境》2009,28(5):96-98,103
“5·12”汶川特大地震发生后。带来的植被破坏、水土流失、次生地质灾害等,给灾区生态环境造成了极大的影响。本文重点以汶川县作为典型区域,运用“3S”技术,通过对汶川县震前、震后的生态环境状况及其变化情况进行定量评价。分析“5·12”大地震对龙门山区生态环境的影响,以期为区域灾后重建提供参考。  相似文献   
140.
Endosulfan in China 1—gridded usage inventories   总被引:9,自引:0,他引:9  
Background, aim, and scope  Endosulfan, an organochlorine pesticide (OCP), is genotoxic in mammalian cells and generally considered to be toxic and classified by the World Health Organization and the US Environmental Protection Agency as priority pollutants and a nominator for inclusion in a future iteration of the persistent organic pollutants treaty. Endosulfan is a currently used pesticide and still being used worldwide. The general trend of total global endosulfan use has increased continuously since the first year when this pesticide was applied. It is critical to create national endosulfan usage/emission inventories for China to carry out source–receptor relation analysis, risk assessment, and other research related to endosulfan in this country. Chinese inventories have been published for some OCPs, such as technical HCH and lindane, DDT, and chlordane; for endosulfan, however, there has not been any usage inventory available on any scales (national or provincial), although endosulfan has been widely used since 1994 in this country. This is the first part of the work. The goal of this paper is to quantify the historical production and usage of endosulfan in China and to compile gridded historical usage inventories of endosulfan for this country. Based on these usage inventories, emission and residue inventories will be created, which is the goal of the second part of the work. Materials and methods  Due to the lack of national production and usage information of endosulfan in China, a method to estimate the use of endosulfan was developed. First, information of crops on which endosulfan is applied and average endosulfan use and annual application frequencies of endosulfan on these crops were collected. Secondly, usage of endosulfan on each crop was estimated using the national cropland area for each province from Chinese government reports. Finally, with the help of GIS (geographic information system), the usage data of this insecticide was allocated to a grid system, with a 1/4° longitude by 1/6° latitude resolution, with a size for each grid cell of approximately 25 km by 25 km. Results and discussion  The use of endosulfan in agriculture in China started on cotton in 1994, and on wheat, tea, tobacco, apples, and other fruits in 1998. Endosulfan usage on cotton, wheat, tea, tobacco, and apples in China has been estimated to be approximately 25,700 t between 1994 and 2004. The province with the highest usage of endosulfan is Henan Province, with a total usage reaching 4,000 t, followed by the uses in Xinjiang Autonomous Region (3,200 t), Shandong Province (3,000 t), Hebei Province (2,100 t), and Anhui Province (1,900 t). Gridded usage inventories of endosulfan at a 1/4° longitude by 1/6° latitude resolution have been created, which indicate that the intensive endosulfan use was in the south of Hebei Province, west of Shandong Province, east of Henan Province, north of Anhui Province, east of Jiangsu Province, and some areas in Yunnan Province and Xinjiang Autonomous Region. General agreement has been found between the usage data from our estimation and the small amount of usage data published in China. Conclusions  This is the first national gridded endosulfan usage inventory produced for China. The annual applications of endosulfan from 1994 to 2004 in China were estimated based on the total areas of major crops, on which endosulfan was applied, and spatial distribution of the application was generated at provincial and prefecture levels. With the help of GIS, endosulfan usage based on prefecture was transferred to a 1/4° longitude by 1/6° latitude gridding system. The satisfaction of the inventories was supported by the consistence between the estimation of the annual usage and the reported annual production of endosulfan. Recommendations and perspectives  This gridded endosulfan usage inventory created in this study will be improved upon availability of new information of endosulfan. The usage inventories can be used to create gridded emission and residue inventories for this insecticide. It is believed that this work will pave the way for further endosulfan studies in China and beyond.  相似文献   
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