长白山森林景观破碎的遥感探测(英文)

天然林数量的减少以及质量的降低对中国的生态环境和经济发展产生不利影响。虽然林地的破碎对各种自然灾害起到关键性作用 ,林地是如何被破碎的尚不十分清楚。应用卫星遥感技术 ,以及地理信息系统和空间分析手段研究中国东北一原始的针阔混交林的破碎过程。结果表明 ,本来完整的原始森林 ,已经被一种“复叶”状小面积皆伐作业分割为零碎的斑块。采伐地的面积平均为 1 5 hm2 ,但随着采伐的继续 ,采伐地段连为一体 ,增大了采伐迹地的面积 ,从而保留的林地面积越来越小。采伐地点的选择没有考虑物种和环境的保护。林地破碎的特征是保留林地面积的缩小 ,中、小林地数量的增加 ,林地斑块形状的改变 ,以及林缘长度的增加。最后就保护东北森林植被完整性的角度提出林业政策与森林经营的改进意见

喀斯特高原山区的景观格局变化垂直分异性——以贵州省普定后寨地下河流域中下游为例

利用多时相多数据源遥感影像数据(航片、TM影像及SPOT-5影像),采用GIS空间分析技术和数理统计分析相结合的方法,以贵州省普定县后寨地下河流域中下游地区为例,从海拔和坡位2个方面来探讨喀斯特地区的景观格局变化的垂直分异特征。结果表明:林地斑块在海拔范围为1300~1350 m及1450~1550 m的区域内,变化是最大的;水田和旱地斑块在海拔范围为1219~1300 m及1350~1450 m的区域内,变化最大。景观格局在山脊和谷底内变化相对较大,其中变化最大的是林地斑块;景观格局在陡坡和缓坡地区的变化相对较小,但是也存在一定的变化,该区域中变化较大的为水田和旱地斑块。在海拔范围为1300~1500 m的山脊和谷底区域内,景观斑块类型发生的变化较大。该区域应作为喀斯特高原山区的生态环境保护特别关注的区域。

黄土高原不同演替阶段草地植被细根垂直分布特征与土壤环境的关系

研究了黄土区不同演替阶段草地植被细根垂直分布特征与土壤环境的关系,结果表明不同演替阶段草地植被细根生物量、根长密度、表面积、直径和比根长均具有明显的垂直分布特征。细根生物量、根长密度和细根表面积一般随土层加深而逐渐减少,且集中分布于0~40cm土层;随着演替的进行,除20a弃耕地外,0~80 cm土层细根生物量、根长密度和细根表面积逐渐增加;除25a弃耕地外,细根直径随演替进行逐渐减小。0~100 cm土层土壤含水量随演替进行而增加,不同演替阶段深层土壤水分较表层稳定。土壤容重的变化趋势为9<4<15<20<25a弃耕地,根系对表层土壤水分和容重的影响较大,而对深层土壤水分与容重影响较少。不同演替阶段细根各参数和土壤水分、容重差异均达到显著水平。各弃耕地细根参数之间,细根参数和土壤环境因子之间存在不同程度的相关关系,土壤含水量在草本植被的不同演替阶段均是影响其细根垂直分布的关键因素。土壤容重在演替早期对草本植被根系的影响较小,随着演替进行其影响作用进一步增强。

用二进小波分析方法对华北地区强震活动期的研究

利用二进小波变换对华北地区1300～1996年的强震时间序列进行了多尺度分解,并据此划分了不同的地震活动期。认为公元1300年之后,华北地区的强震存在两个平静期(1350～1450年、1700～1780年)和两个活跃期(1450～1700年、1780～1996年)。与以往华北强震的活动期划分方案进行比较,本文的结果在总体规律上与以前的研究差别不大,但在第三、第四地震活动期中活跃期起始界限的划分上比其它方法略有提前,而在平静期的划分上相对较短。文中采用32a尺度的小波分析信号进行分析,既考虑了较大尺度上地震

Phase separation and crystallization in a melt-spun Ti45Zr35Ni17Cu3 alloy

Structure and crystallization behavior of amorphous and quasicrystalline Ti45Zr35Ni17Cu3 alloy have been studied. DSC trace of the amorphous alloy obtained during continuous heating to 1300 K shows distinctly an exothermic peak and two endothermic peaks.

Self-Assembled Growth of Agln(MoO4)(2) Submicroplates into Hierarchical Structures and Their Near-Infrared Luminescent Properties

Layer-controlled hierarchical flowerlike AgIn(MoO4)(2) microstructures with "clean" surfaces using submicroplates as building blocks without introducing any template have been fabricated through a low-cost hydrothermal method. The near-infrared luminescence of lanthanide ion (Nd, Er, and Yb) doped AgIn(MoO4)(2) microstructures, in the 1300-1600 nm region, was discussed and is of particular interest for telecommunication applications. X-ray diffraction, scanning electron microscopy, transmission electron microscopy, electron diffraction, and photoluminescence spectra were used to characterize these materials.

CuIn(WO4)(2) nanospindles and nanorods: controlled synthesis and host for lanthanide near-infrared luminescence properties

CuIn(WO4)(2) porous nanospindles and nanorods were synthesized through a low-cost hydrothermal method without introducing any template or surfactants. An interesting formation mechanism, namely "oriented attachment", was observed for the growth of nanorods based on the experimental process and the anisotropic intrinsic crystalline structure of CuIn(WO4)(2), which is uncommon in such a system. The near-infrared luminescence of lanthanide ions (Er, Nd, Yb and Ho) doped CuIn(WO4)(2) nanostructures, especially in the 1300-1600 nm region, was discussed and of particular interest for telecommunications applications. X-Ray diffraction, scanning electron microscopy, transmission electron microscopy, electron diffraction and photoluminescence spectra were used to characterize these materials.

Synthesis and chain-length dependent properties of monodisperse oligo(9,9-di-n-octylfluorene-2,7-vinylene)s

A series of monodisperse oligo(9,9-di-n-octylfluorene-2,7-vinylene)s (OFVs) with fluorene units up to 11 has been synthesized following a divergent approach. Chain length was found to affect not only photophysical properties but also thermal properties. Absorption and photoluminescence spectra are red-shifted with increasing chain length. The effective conjugated length has been extrapolated to be as long as 19 fluorene vinylene units, indicative of a well-conjugated system. With the number of fluorene units > 5, the oligomers exhibit nematic mesomorphism. Glass transition temperature (T-g) and clearing point temperature (T-c) increase with increasing molecular length and with those of OFV11 up to 71 and 230 degrees C, respectively. The oligomers can form uniform films by solution casting for fabrication of light-emitting diodes. With a device structure of ITO/ PEDOT:PSS/OFV11/Ca/Al, a current efficiency of 0.8 cd.A(-1) at a brightness of 1300 cd.m(-2) along with a maximum brightness of 2690 cd.m(-2) have been realized. This performance is notably superior to that of the corresponding polymer.

Near-infrared luminescent mesoporous materials covalently bonded with ternary lanthanide [Er(III), Nd(III), Yb(III), Sm(III), Pr(III)] complexes

New near-infrared-luminescent mesoporous materials were prepared by linking ternary lanthanide (Er3+, Nd3+, Yb3+, Sm3+, Pr3+) complexes to the ordered mesoporous MCM-41 through a functionalized 1,10-phenanthroline (phen) group 5-(N,N-bis-3-(triethoxysilyl)propyl)ureyl-1,10-phenanthroline. The resulting materials (denoted as Ln(hfth)(3)phen-M41 and Pr(tfnb)(3)phen-M41; Ln=Er, Yb, Nd, Sm; hfth = 4,4,5,5,6,6,6-heptafluoro-1-(2-thienyl)hexane-1,3-dionate; tfnb = 4,4,4-trifluoro-1-(2-naphthyl)- 1, 3-butanedionate) were characterized by powder X-ray diffraction, N-2 adsorption/desorption, and elemental analysis. Luminescence spectra of these lanthanide-complex functionalized materials were recorded, and the luminescence decay times were measured. Upon excitation at the absorption of the organic ligands, all these materials show the characteristic NIR luminescence of the corresponding lanthanide (Er3+, Nd3+, Yb3+, Sm3+, Pr3+) ions by sensitization from the organic ligands moiety. The good luminescent performances enable these NIR-luminescent mesoporous materials to have possible applications in optical amplification (operating at 1300 or 1500 nm), laser systems, or medical diagnostics.

Processing, microstructure and mechanical properties of W50Al50 bulk alloy obtained by mechanical alloying and hot-pressing

The Al50W50 alloy bulk bodies were fabricated by using mechanical alloying and hot-pressing in this work. The Al50W50 alloy had excellent thermal stability up to 1300 degreesC under vacuum and Its optimum microhardness, bending strength and compressive strength were 10.21 GPa, 570 MPa and 2.07 GPa, respectively.

Synthesis and characterization of a novel biodegradable, thermoplastic polyurethane elastomer

A series of biodegradable, thermoplastic polyurethane elastomers poly (epsilon-caprolactone-co-lactide)polyurethane [PCLA-PU] were synthesized from a random copolymer Of L-lactide (LA) and epsilon-caprolactone (CL), hexamethylene diisocyanate, and 1,4-butanediol. The effects of the LA/CL monomer ratio and hard-segment content on the thermal and mechanical properties of PCLA-PUs were investigated. Gel permeation chromatography, IR, C-13 NMR, and X-ray diffraction were used to confirm the formation and structure of PCLA-PUs. Through differential scanning calorimetry, tensile testing, and tensile-recovery testing, their thermal and mechanical properties were characterized. Their glass-transition temperatures were below -8 degrees C, and their soft domains became amorphous as the LA content increased. They displayed excellent mechanical properties, such as a tensile strength as high as 38 MPa, a tensile modulus as low as 10 MPa, and an elongation at break of 1300%. Therefore, they could find applications in biomedical fields, such as soft-tissue engineering and artificial skin.

Phenylene vinylene-based electroluminescent polymers with electron transport block in the main chain

We report a new route for the design of soluble phenylene vinylene (PV) based electroluminescent polymers bearing electron-deficient oxadizole (OXD) and triazole (TZ) moieties in the main chains with the aryloxy linkage. Both series of the PV-based polymers were prepared by Wittig reaction. By properly adjusting the OXD and/or TZ content through copolymerization, we can achieve an enhanced balance of hole- and electron injections, such that the device efficiency is significantly improved. Light-emitting diodes fabricated from P1, P2, P3, P4, P5, P6, and P7 with the configuration of Indium-Tin Oxide (ITO)/Poly (styrene sulfonic acid) doped poly (ethylenedioxythiophene) (PEDOT)/polymer/Ca/Al, emit bright green light with the maximum peak around 500 nm. For the device using the optimal polymer (P4) as emitting layer, a maximum brightness of 1300 cd/m(2) at 20 V and a maximum luminance efficiency of 0.325 cd/A can be obtained.

Syntheses, structures and near-IR luminescent studies on ternary lanthanide (Er-III, Ho-III, Yb-III, Nd-III) complexes containing 4,4,5,5,6,6,6-heptafluoro-1-(2-thienyl)hexane-1,3-dionate

The ligand Hhfth [4,4,5,5,6,6,6-heptafluoro-1-(2-thienyl)hexane-1,3-dione], which contains a heptafluoropropyl group, has been used to synthesize several new ternary lanthanide complexes (Ln = Er, Ho, Yb, Nd) in which the synergistic ligand is 1,10-phenanthroline (phen) or 2,2'-bipyridine (bipy). The two series of complexes are [Ln(hfth)(3)phen] [abbreviated as (Ln)1, where Ln = Er, Ho, Yb] and [Ln(hfth)(3)bipy] [abbreviated as (Ln)2, where Ln = Er, Ho, Yb, Nd]. Members of the two series have been structurally characterized. The growth morphology, diffuse reflectance (DR) spectra, thermogravimetric analyses, and photophysical studies of these complexes are described in detail. After ligand-mediated excitation of the complexes, they all show the characteristic near-infrared (NIR) luminescence of the corresponding Ln(3+) ions (Ln = Er, Ho, Yb, Nd). This is attributed to efficient energy transfer from the ligands to the central Ln(3+) ions, i.e. an antenna effect. The heptafluorinated substituent in the main hfth sensitizer serves to reduce the degree of vibrational quenching. With these NIR-luminescent lanthanide complexes, the luminescent spectral region from 1300 to 1600 nm, which is of particular interest for telecommunication applications, can be covered completely.

Induction effect of Ca2+ on ion-channel behavior of supported phospholipid membranes

As a kind of supported bilayer lipid membranes, hybrid bilayer membrane (HBM) was applied to the interaction between Ca2+ and lipid for the first time. By using Fe(CN)(6)(3-) as a probe, we found that Ca2+ could induce the ion channel of HBM to be in open state. STM images study proved this phenomenon.