大兴安岭呼中林区地表死可燃物载荷量空间格局

利用地统计学方法,依据时滞分类标准对大兴安岭呼中林区地表死可燃物进行了对比研究.结果表明:一级地表死可燃物表现为强烈的空间自相关性,占总地表死可燃物载荷量的55.54%,平均载荷量为762.35g·m-2,其载荷量的决定因素是林分因子和立地年龄;二、三级地表死可燃物的平均载荷量之和为610.26g·m-2,具有较弱的空间自相关性,其载荷量的决定因素为干扰历史.地表死可燃物类型和数量影响因素的复杂性和空间异质性是造成插值精度不高的主要原因,但采用实地调查数据,并结合地统计学方法,可快速准确地计算出地表死可燃物载荷量的空间分布格局,可间接为林业管理提供依据.

甘肃省苔类植物初步研究

通过对甘肃省所采集苔类植物标本的鉴定和统计整理,共报道苔类植物18科30属78种及变种,其中包括3个新记录科,分别为:扁萼苔科(Radulaceae)、魏氏苔科(Wiesnerellaceae)、带叶苔科(Pallavicinaceae),11个新记录属和35个新记录种;区系分析表明北温带成分占据优势(占总种数的43.24%),其次是东亚成分(占总种数的22.97%),甘肃省苔类植物区系具有明显的温带性质。

Introduction to Molecular Analysis of Ectomycorrhizal Communities

A number of methods are available for those researchers considering the addition of molecular analyses of ectomycorrhizal (EcM) fungi to their research projects and weighing the various approaches they might take. Analyzing natural EcM fungal communities has traditionally been a highly skilled, time-consuming process relying heavily on exacting morphological characterization of EcM root tips. Increasingly powerful molecular methods for analyzing EcM communities make this area of research available to a much wider range of researchers. Ecologists can gain from the body of work characterizing EcM while avoiding the requirement for exceptional expertise by carefully combining elements of traditional methods with the more recent molecular approaches. A cursory morphological analysis can yield a traditional quantification of EcM fungi based on tip numbers, a unit with functional and historical significance. Ectomycorrhizal root DNA extracts may then be analyzed with molecular methods widely used for characterizing microbiota. These range from methods applicable only to the simple mixes resulting from careful morphotyping, to community-oriented methods that identify many types in mixed samples as well as provide an estimate of their relative abundances. Extramatrical hyphae in bulk soil can also be more effectively studied, extending characterization of EcM fungal communities beyond the rhizoplane. The trend toward techniques permitting larger sample sets without prohibitive labor and time requirements will also permit us to more frequently address the issues of spatial and temporal variability and better characterize the roles of EcM fungi at multiple scales.

旱地长期培肥土壤脲酶和碱性磷酸酶动力学及热力学特征研究

研究了连续25年长期培肥试验条件下土壤脲酶和碱性磷酸酶酶促反应的动力学和热力学特征,从酶学角度揭示长期培肥的效应。结果表明,长期培肥增加了脲酶和碱性磷酸酶酶促反应的Vmax、Vmax/Km和k值;降低了Ea、△G、△H和△S值,说明培肥能提高酶促反应速度、减小活化自由能、加快土壤中物质的生物循环过程。酶促反应动力学参数和热力学参数与土壤性质相关分析表明,酶促反应动力学参数大多依赖于土壤化学性状,基于动力学参数的土壤肥力指标体系可评价土壤肥力水平,且U-Vmax、P-Km、P-Vmax可作为土壤肥力的重要指标。

1、蜜蜂嗅觉学习记忆应用基础研究 2、吗啡和胆碱能拮抗剂联合给药对小鼠Y迷宫空间记忆提取及活动性的影响

一、蜜蜂嗅觉学习记忆应用基础研究特殊气味的探测在刑侦工作中意义重大，常用的警犬探测和仪器分析都有其局限之处。蜜蜂嗅觉灵敏，且学习记忆能力突出，具有为刑侦工作所用的潜力。基于此，我们希望通过训练蜜蜂将其对糖水奖励的伸喙反应与指定气味建立条件反射的原理，配合适当的训练方法，达到利用蜜蜂探测危险气味的目的。在实验中，我们首先比较了不同喂养方式的蜜蜂在气味学习中的差别。由于低浓度气味无法直接使蜜蜂建立条件化，我们采用了逐渐降低气味浓度的方法，成功训练蜜蜂对低浓度(3.6×10-7) 醋酸气味建立了条件反射。结果如下： 1)自然放养与人工孵化两种不同喂养方式的蜜蜂，各两组，分别学习醋酸CS+/薄荷CS-，或柠檬CS+/薄荷CS-的气味配对。以“获得(CS+)，巩固(CS-/CS+ CS+/CS- CS-/CS+)，检测，干净空气假阳性检测”的顺序操作。结果显示自然放养蜜蜂对醋酸气味没有偏好（第一次给醋酸气味伸喙率：6%），学习醋酸气味能力较低（24小时后检测正确率：66%， n=25），相对应，该类蜜蜂对柠檬气味显示出明显偏好(第一次给柠檬气味伸喙率：41%，P< 0.01)，而学习效果（检测正确率：50%，n=20）与醋酸组相近(P>0.05)。人工孵化的蜜蜂对醋酸气味学习能力较自然放养蜜蜂大大提高（检测正确率：96%, n=32， P<0.01），同时对柠檬的学习结果（检测正确率：80%, n=32）也明显提高(0.01

Reversed micelle formation in a model liquid-liquid extraction system

The formation of reversed micelles and the roles of extractant and extracted complexes were investigated in the Cyanex923/n-heptane/H2SO4 system. Interfacial tension (gamma), electrical conductivity (kappa), and water content measurements showed that Cyanex923 had a tendency to self-assemble, forming reversed micelles. The changes in electrical conductivity with concentration of H2SO4 in the organic phase (CH2SO4,(0)) exhibited an S-type curve: a correlation was found between the change in electrical conductivity and the water content as a function of CH2SO4,(0),.

Y2O3 : Eu3+ microspheres: Solvothermal synthesis and luminescence properties

Y2O3 : Eu3+ microspheres, with an average diameter of 3 mu m, were successfully prepared through a large-scale and facile solvothermal method followed by a subsequent heat treatment. X-ray diffraction, Fourier transform infrared spectroscopy, energy-dispersive X-ray spectra, thermogravimetric and differential thermal analysis, inductive coupled plasma atomic absorption spectrometric analysis, scanning electron microscopy, transmission electron microscopy, photoluminescence spectra, as well kinetic decays, and cathodoluminescence spectra were used to characterize the samples. These microspheres were actually composed of randomly aggregated nanoparticles. The formation mechanisms for the Y2O3 : Eu3+ microspheres have been proposed on an isotropic growth mechanism. The Y2O3 : Eu3+ microspheres show a strong red emission corresponding to D-5(0) -> F-7(2) transition (610 nm) of Eu3+ under ultraviolet excitation (259 nm) and low-voltage electron beams excitation (1-5 kV), which have potential applications in fluorescent lamps and field emission displays.

The luminescence of CaYBO4 : RE3+ (RE=Eu, Gd, Tb, Ce) in VUV-visible region

Phosphors CaYBO4:RE3+ (RE = Eu, Gd, Tb, Ce) were synthesized with the method of solid-state reaction at high temperature, and their vacuum ultraviolet (VUV)-visible luminescent properties in VUV-visible region were studied at 20 K. In CaYBO4, it is confirmed that there are two types of lattice sites that can be substituted by rare-earth ions. The host excitation and emission peaks of undoped CaYBO4 are very weak, which locate at about 175 and 350-360nm, respectively. The existence of Gd3+ can efficiently enhance the utilization of host absorption energy and result in a strong emission line at 314 nm. In CaYBO4, Eu3+ has typical red emission with the strongest peak at 610 nm; Tb3+ shows characteristic green emission, of which the maximum emission peak is located at 542 nm. The charge transfer band of CaYBO4:Eu3+ was observed at 228 nm; the co-doping of Gd3+ and Eu3+ can obviously sensitize the red emission of Eu3+. The fluorescent spectra of CaYBO4:Ce3+ is very weak due to photoionization; the co-addition of Ce3+-Tb3+ can obviously quench the luminescence of Tb3+.

Synthesis and luminescence properties of nanocrystalline Gd2O3 : Eu3+ by combustion process

The nanocrystalline Gd2O3:Eu3+ powders with cubic phase were prepared by a combustion method in the presence of urea and glycol. The effects of the annealing temperature on the crystallization and luminescence properties were studied. The results of XRD show pure phase can be obtained, the average crystallite size could be calculated as 7, 8, 45, and 23 run for the precursor and samples annealed at 600, 700 and 800 degrees C, respectively, which coincided with the results from TEM images. The emission intensity, host absorption and charge transfer band intensity increased with increasing the temperature. The slightly broad emission peak at 610 nm for smaller particles can be observed. The ratio of host absorption to O-2-Eu3+ charge transfer band of smaller nanoparticles is much stronger compared with that for larger nanoparticles, furthermore, the luminescence lifetimes of nanoparticles increased with increasing particles size. The effects of doping concentration of Eu3+ on luminescence lifetimes and intensities were also discussed. The samples exhibited a higher quenching concentration of Eu3+, and luminescence lifetimes of nanoparticles are related to annealing temperature of samples and the doping concentration of Eu3+ ions.

Controlled organization of silver nanoparticles into network assemblies by tuning pH values

We demonstrate the pH-induced assembly of 2-mercaptosuccinic acid-functionalized silver nanoparticles (MSA-Ag NPs) in the absence of hard or soft template. Two-dimensional (2D) and three-dimensional (3D) networks of silver NPs were achieved by tuning pH of the medium. The assembly process was monitored using atomic forces microscopy. The key factor affects the formation of network of silver NPs may be intermolecular hydrogen bonding between two carboxylic acid groups of MSA on two adjacent silver NPs.

Synthesis and luminescence properties of Gd2O3 : Eu3+ phosphors

Gd2O3: EU3+ phosphors were prepared by urea homogeneous precipitation with different surfactant and sol-gel method. XRD patterns show that all the obtained samples are in cubic Gd2O3, and the results of FTIR and fluorescent spectra conformed that OP is a good surfactant for preparing the Gd2O3: Eu3+ phosphors. The SEM photographs show that the particles prepared by urea homogeneous precipitation method are all spherical and well-dispersed, and grain morphology can be controlled by different surfactant. XRD and SEM indicate that the particle sizes prepared by sol-gel method are in the range of 5 similar to 30 nm, and the grain sizes increase with increasing of heated temperatures. Luminescence spectra indication that the main emission peaks of all samples are at 610 nm, the intensities are different from samples prepared with different surfactant and the luminescence intensities increase with increasing of annealed temperatures.

Ordered macroporous films from self-assembly of two-armed polymer with a crown ether core

Highly ordered honeycomb-like macroporous films were obtained via self-assembly of a two-armed polymer with a crown ether core under controlled conditions. A possible mechanism is speculated, primarily based on the strong affinity between the crown ether cores. The pore size and arrangement are sensitive to the solvent evaporation rate and the solution concentration. Upon spontaneous drying, the pore diameter (D) depends on the concentration (c) by a relation of D=518c(-0.610).

Computer simulation of Gd(III) speciation in human interstitial fluid

The speciation and distribution of Gd(III) in human interstitial fluid was studied by computer simulation. The results show that at the background concentration, all the Gd(III) species are soluble and no precipitates appear. However as the total concentration of Gd(III) rises above 2.610 x 10(-9) mol/l the insoluble species become predominant. GdPO4 is formed first as a precipitate and then Gd-2(CO3)(3). Among soluble species, free Gd(III), [Gd(HSA)], [Gd(Ox)] and the ternary complexes of Gd(III) with citrate as the primary ligand are main species when the total concentration of Gd(III) is below 2.074 x 10(-2) mol/l. With the total concentration of Gd(III) further rising, [Gd-3(OH)(4)] begins to appear and gradually becomes a predominant species.

Peripheries of molecular projection in three-dimensional space and studies of quantitative structure-activity relationships

A new index, i.e., the periphery representation of the projection of a molecule from 3D space to a 2D plane is described. The results, correlation with toxicity of substituted nitrobenzenes, obtained by using periphery descriptors are much better than that obtained by using the areas (i.e., shadows) of projections of the compounds. Even better results were achieved by using the combination of periphery descriptors and the projections areas as well as the indicated variable K reflecting the action of group NO position on the benzene ring.