武汉市城郊乡村旅游地的类型划分及时空分布特征研究

在对武汉市城郊534个乡村旅游地进行类型划分的基础上，运用数理统计和空间分析法，对其时空分布特征和影响因素进行研究，得出以下结论：(1）武汉市城郊乡村旅游地在发展过程中，呈现出四个明显的发展时段，旅游极化发展形成的空间冷热点区随时间而发生变化，现已在武汉市西北、西部和南部形成三大旅游集聚区。（2）武汉市城郊乡村旅游地类型日益多元化，从发展初期的休闲观光和乡村文化两种类型逐步增加至休闲观光、乡村文化、农事体验、农业科技、特色村镇等五种类型；不同类型的乡村旅游地发展速度、规模、极化趋势各异。(3）与中心城区距离、相关政策、道路交通条件、水文因素、旅游资源禀赋等均对乡村旅游地的时空分布特征产生影响，各个因素对不同类型旅游地时空分布的影响存在一定差别。     

曲霉菌降解机械润滑油的研究

分离出能高效降解机油的真菌并研究其使用方法.从机械润滑油污染的土中分离出2株真菌,GXUA和GXUB.形态鉴定为曲霉属(Aspergillus)菌.rDNA的ITS序列同源性分析表明,GXUA与A.tubingens,GXUB与A.fumigatus菌株SRRC 43完全同源.根据均匀设计的油-矿质液中的摇床发酵结果,混合菌体对机油的降解效率高于单菌株,最佳发酵条件为25 g菌丝体/L矿质液,pH=5.0,26 ℃.在此条件下,于10 g机油/L矿质液中摇床发酵9 d,其降解效率为95.90%.液-质色谱分析表明,混合菌能降解机油中700～900 Dt的大分子.用两菌株的孢子和其他两种生物材料试制了实验室级的颗粒(直径1 cm)生物制剂.在实验室级水平上,按500粒/m2水面和150粒/kg土用量分别处理具有约2 mm厚油膜的水(自来水和海水)和50 g机油/kg土的土壤,处理后的水和土壤中残余油量符合国家有关环境污染控制标准,添加油酸钠和H2O2能够显著提高降解效率.     

空调压缩机冷媒爆炸反应特征分析

冷媒与空气的反应特征对空调压缩机安全性有重要影响.本文采用最小自由能原理,分别对两种冷媒R407C和R410A与空气的混合气体的爆炸反应参数进行了数值计算,得到了不同初始压力和不同冷媒含量条件下,混合气体爆炸反应温度和压力,分析了混合气体反应压力条件和爆炸极限范围.结果表明:初始压力低于0.2 MPa时,R407C-空气混合气体和R410A-空气混合气体均不会发生爆炸;初始压力超过0.3 MPa时,混合气体能够发生爆炸,爆炸反应温度和压力随着初始压力的升高而升高;R407C和R410A质量分数分别在34%、35%左右,混合气体反应温度和压力达到最大值.R407C和R410A易燃易爆特征相近;但爆炸范围都比氟利昂(R22)气体宽,即同样的条件下更容易发生爆炸.该计算结果能够为新型冷媒R407C和R410A的安全使用提供一定的依据.     

大气臭氧浓度升高对丛枝菌根(AM)及其功能的影响

通过模拟大气O₃浓度(0.02μL·L^-1、0.1μL·L^-1和0.2μL·L^-1)升高,观察其对丛枝菌根(AM)及功能的影响.结果表明,大气O₃浓度升高对菌根侵染率影响较小,但对孢子和外生菌丝影响显著,高浓度O₃时的孢子数比自然O₃浓度时增加1倍,低、高浓度O₃分别使AM外生菌丝量比自然浓度时下降48.7%和85.6%.随着O相似文献   

Effect of arsenic on chloroplast ultrastructure and calcium distribution in arsenic hyperaccumulator Pteris vittata L

This study investigated the impacts of arsenic (As) on the chloroplast ultrastructure and calcium (Ca) distribution in Chinese brake (Pteris vittata L.) mainly by histochemical methods, with an emphasis on the possible function of Ca in As detoxification and accumulation in P. vittata. P. vittata was grown in an artificially contaminated soil added with different concentrations of Na(2)HAsO(4) (0, 100, 300 and 800 mg kg(-1) As dry soil) for 24 weeks in a greenhouse. The addition of As did not affect the chloroplast ultrastructure of young pinna, meanwhile most of the membrane systems of chloroplasts in mature pinna were severely damaged under high As condition. Calcium concentration in the fronds of P. vittata was not significantly affected by the addition of As, but Ca concentration in the mature pinna significantly increased by As addition, consistent with the position appearing As toxicity. When no As was added, most of calcium precipitates distributed around the inner membrane of vacuole. But when the pinna appeared plasmolysis, more calcium precipitates resided outside the cell membrane and bigger particles evenly distributed in the cytoplasm. All the results indicated that Ca had a close relation with As toxicity in P. vittata.     

Zinc tolerance and accumulation in Pteris vittata L. and its potential for phytoremediation of Zn- and As-contaminated soil

A field investigation and pot experiments were conducted to determine the potential of arsenic (As) hyperaccumulator, Pteris vittata L., to remediate sites co-contaminated with zinc (Zn) and As. We found that P. vittata L. had a very high tolerance to Zn and grew normally at sites with high Zn concentrations. In addition, P. vittata L. could effectively take up Zn into its fronds, with a maximum of 737 mg kg(-1) under field conditions. In pot experiments, the accumulated Zn concentration increased significantly as the Zn treatment was raised from 0 to 2000 mg kg(-1), with a maximum Zn accumulation of 0.22 mg pot(-1). Although the concentration of As in P. vittata L. was reduced by the addition of Zn, total frond accumulation of As was elevated when the Zn treatment was increased from 0 to 1000 mg kg(-1), with a maximum As accumulation of 8.3 mg pot(-1) in the presence of 1000 mg kg(-1) Zn. The high Zn tolerance, relatively high ability to accumulate Zn, and great capacity to accumulate As under conditions of suppression by high Zn suggest that P. vittata L. could be useful for the remediation of sites co-contaminated with Zn and As.     

Polycyclic aromatic hydrocarbons (PAHs) in the aerosol in Beijing, China, measured by aminopropylsilane chemically-bonded stationary-phase column chromatography and HPLC/fluorescence detection

We developed a useful analytical method for the determination of polycyclic aromatic hydrocarbons (PAH) concentrations in the aerosol of China. We used an accelerated solvent extraction (ASE) method for the extraction of PAHs from the aerosol samples, in order to reduce the extraction time and the solvent volume used. The optimum purification method was developed, with aminopropylsilane chemically-bonded stationary-phase column chromatography, in order to remove many co-extractives which cannot be removed by conventional purification methods using silica-gel column chromatography. HPLC/fluorescence detection (FLD) was adopted as the analytical method, because it has very high sensitivity to PAH and it is easy to install, operate, and maintain as compared with GC/MS. With the analytical method developed in this study, the recovery and precision (RSD) for most of the PAHs ranged from 75% to 129% and from 2.8% to 22.7%, respectively. The concentrations of PAHs in the aerosol samples collected from October 2003 to April 2005 in Beijing, China were determined using the newly developed method. SigmaPAHs, which is the sum of the concentrations of all detected PAHs, was 177.8 +/- 239.9 ng m(-3) (n = 64). The SigmaPAHs concentration in the heating season (305.1 +/- 279.0 ng m(-3), n = 33) was 7.2 times higher than that in the non-heating season (42.3 +/- 32.0 ng m(-3), n = 31). These strong seasonal variations in atmospheric PAH concentration are possibly due to coal combustion for residential heating in winter.     

简化连续提取法评价污染土壤中Zn、Cd的植物有效性

以0.01 mol·L^-1CaCl₂和0.005 mol·L^-1 DTPA作为提取剂,用简化的3步连续提取法对贵州省赫章县土法炼锌污染土壤中Zn、Cd的形态进行了分析.结果显示,污染土壤中Zn、Cd主要以残渣态的形式存在,CaCl₂提取态和DTPA提取态Zn、Cd平均仅占全量的0.63%、3.91%和10.94%、10.13%.土壤中不同形态Zn、Cd含量与玉米中Zn、Cd含量的相关分析结果显示,CaCl₂提取态金属与玉米中金属含量没有显著的相关关系,而DTPA提取态、残渣态以及总量Zn、Cd与玉米根、茎叶中Zn、Cd含量显著正相关.这些结果表明CaCl₂提取态Zn、Cd对土壤中该元素的植物有效态可能不具重要贡献,而DTPA提取态金属和金属总量在一定程度上能作为评价土壤中元素植物有效性的标准.     

恶臭假单胞菌Pseudomonas putida 5-x细胞壁膜系统的Cu2+吸附性能

对1株从电镀废水中分离出的革兰氏阴性菌恶臭假单胞菌P.putida 5-x的细胞表面组分对Cu²⁺的吸附性能进行了分析研究.结果表明,分离的P.putida 5-x细胞壁膜的Cu²⁺吸附容量是完整细胞的5倍之多.细胞表面组分如肽聚糖层、细胞外膜和细胞内膜在P.putida 5-x细胞壁膜的Cu²⁺吸附过程中都发挥了作用.肽聚糖层、细胞外膜和内膜在P.putida 5-x细胞壁膜中的含量依次为细胞内膜>外膜>肽聚糖层,而它们的Cu²⁺吸附容量的大小依次为肽聚糖层>外膜>内膜.在P.putida 5-x细胞壁膜对Cu²⁺的吸附过程中,肽聚糖层贡献了不到15%的吸附容量,而细胞外膜和内膜分别贡献了30%～35%和25%～30%.P.putida 5-x细胞外膜中的磷脂含量明显比其它报道的革兰氏阴性细菌的细胞外膜高,这可能是P.putida 5-x细胞外膜具有较高Cu²⁺吸附容量的主要原因,并由此导致P.putida 5-x细胞壁膜的高Cu2+吸附容量.     

Quantitation of Hydroxyl Radicals from Photolysis of Fe(III)-Citrate Complexes in Aerobic Water (5 pp)

Background For their high photoreactivity, Fe(III)-carboxylate complexes are important sources of H2O2 for some atmospheric and surface waters. Citrate is one kind of carboxylate, which can form complexes with Fe(III). In our previous study, we have applied Fe(III)-citrate complexes to degrade and decolorize dyes in aqueous solutions both under UV light and sunlight. Results have shown that carboxylic acids can promote the photodegradation efficiency. It is indicated that the photolysis of Fe(III)-citrate complexes may cause the formation of some reactive species (e. g. H2O2 and ·OH). This work is attempted to quantify hydroxyl radicals generated in the aqueous solution containing Fe(III)-citrate complexes and to interpret the photoreactivity of Fe(III)-citrate complexes for degrading organic compounds. Methods By using benzene as the scavenger to produce phenol, the photogeneration of ·OH in the aqueous solution containing Fe (III)-citrate complexes was determined by HPLC. Results and Discussion In the aqueous solution containing 60.0/30.0 mM Fe(III)/citrate and 7.0 mM benzene at pH 3.0, 96.66 mM ·OH was produced after irradiation by a 250W metal halide light (l ≥ 313 nm) for 160 minutes. Effects of initial pH value and concentrations of Fe(III) and citrate on ·OH radical generation were all examined. The results show that the greatest photoproduction of ·OH in the aqueous solution (pH ranged from 3.0 to 7.0) was at pH 3.0. The photoproduction of ·OH increased with increasing Fe(III) or citrate concentrations. Conclusion In the aqueous solutions containing Fe(III)-citrate complexes, ·OH radicals were produced after irradiation by a 250W metal halide light. It can be concluded that Fe(III)-citrate complexes are important sources of ·OH radicals for some atmospheric and surface waters. Recommendations and Outlook It is believed that the photolysis of Fe(III)-citrate complexes in the presence of oxygen play an important role in producing ·OH both in atmospheric waters and surface water where high concentrations of ferric ions and citrate ions exist. The photoproduction of ·OH has a high oxidizing potential for the degradation of a wide variety of natural and anthropogenic organic and inorganic substances. We can use this method for toxic organic pollutants such as organic dyes and pesticides.