岩溶生态系统脆弱性剖析

生态系统的脆弱性评价对于生态系统管理具有重要作用。在分析岩溶生态系统脆弱性特征和影响因素的基础上,构建了针对岩溶自然系统的脆弱性评价指标体系,涵盖了岩溶生态系统的结构脆弱性、生态过程脆弱性、生态功能脆弱性和人为胁迫脆弱性4个方面,评价指标分别是结构稳定性、多样性生境、能量利用和积累、直接使用价值、石漠化程度和速率等。以不同类型的原生岩溶生态系统的生态基准值作为比较基础,评价系统将现有的退化岩溶生态系统的脆弱性划分为轻微脆弱、中度脆弱、重度脆弱以及系统崩溃4级

银和锰之间可能存在的联系

一般认为Ag与Pb、Zn、Cu共生，少数与Au、Sn、Sb、W、As等共生，很少有学者注意到Ag和Nn共生。关于Ag和Nn之间的研究多集中在银锰矿石选矿方面。也有部分学者通过研究渐新世含银矿床中还原锰的离析和生物化学作用。推测前寒武纪的一些生物地球化学作用。从已有的资料看。大多数锰矿床都缺乏银分析数据，过去只认为在表生风化作用下形成的铁-锰帽可能会造成银的富集。并把它划归成铁锰帽型银矿。

岩浆—热液体系成矿流体演化及其金属元素气相迁移研究进展

本文从火山喷气、岩浆热液矿床的成矿流体性质、金属元素在蒸汽相中的溶解及在蒸汽/卤水相的分配实验等方面概述了有关金属元素气相迁移及CO2在成矿过程中作用的研究现状。火山喷气的凝结物中高浓度的Cu、Zn、Pb、As、Ag和Au,以及斑岩型矿床中低密度流体包裹体（蒸汽相）中硫化物矿物的存在,预示着上述金属是以蒸汽相搬运的。金属元素在蒸汽相中溶解实验研究表明,金属元素在蒸汽相中以[Me Xm·（H2O）n]水合物的形式存在,其溶解度随着H2O逸度和HCl逸度的增大而增加;熔体—流体体系分配实验研究揭示,NaCl—H2O体系中存在蒸汽—卤水相分离,在含S条件下Au、As等元素通常以HS-离子络合物的形式优先溶于蒸汽相,Fe、Zn、Pb、Mn、Cs等元素以Cl-离子络合物的形式优先富集于卤水相;Cu在富S热液中优先进入蒸汽相,在富Cl贫S热液中通常富集于卤水相,表明Cu在岩浆热液中是以HS-和Cl-两种络合物的形式迁移的。CO2在Au、Cu等金属元素迁移和沉淀过程中可能起重要的作用,不仅促进NaCl—H2O体系相分离,并且促使HS-络合物在蒸汽相富集以及调节成矿流体的酸碱度。斑岩型Cu—Au矿床的矿化过程可概括为3个阶段：高侵位的斑岩分异出的少量岩浆流体主要形成了青磐岩化带和部分钾硅化带,矿化通常不成规模;深部岩浆房早阶段去气作用分异出的岩浆流体主要在斑岩体早期钾化基础上叠加蚀变并形成广泛的浸染状矿化和石英—硫化物细脉,在斑岩体上部形成高级泥化带并形成低温热液型Cu—Au矿化,此阶段为主矿化期;深部岩浆房晚阶段去气作用形成的岩浆流体可能主要使斑岩体和部分围岩形成绢英岩化,并伴随晚期石英—（方解石）—硫化物脉的沉淀。

贵州织金新华含稀土磷矿床的电子探针研究

位于贵州织金县的新华磷矿是一个超大型磷、稀土综合矿床。已探明磷矿石储量13.148亿吨，稀土氧化物储量144.16万吨。至今稀土元素未找到一条效益理想的综合利用途径.

Synthesis and characterization of manganese-modified MCM-41

Manganese-modified mesoporous MCM-41 molecular sieves were synthesized at the absence of alkaline metal ions under mild alkaline condition using cetylpyridinium bromide surfactant as a template, and characterized with X-ray diffraction, N-2 adsorption, transmission electron microscopy, electron spin resonance (ESR), and nuclear magnetic resonance (NMR) spectroscopies. The synthesized MnMCM-41 has a high pore volume of 1.30 cm(3) g(-1) with a corresponding surface area of 1510 m(2) g(-1). The ESR and Si-29 MAS NMR spectra revealed the presence of framework manganese ions in either the as-synthesized or calcined forms. (C) 2002 Elsevier Science B.V. All rights reserved.

Kinetics of the selective reduction of NO with CH4 over an In-Fe2O3/HZSM-5 catalyst

A kinetic model presented for the selective reduction of NO with CH4 over an InFe2O3/HZSM-5 catalyst by considering the process as a combination of two simultaneous reactions: NO+O2CH4 (reaction 1) and O-2+CH4 (reaction 2). Linear regression calculation was employed to find the kinetic parameters. It was found that although the activation energies of the two reactions were almost identical, the reaction rate constants were dramatically different, namely, k(1)much greater than k(2), indicating that the NO+O-2+CH4 reaction was more preferable to take place on the In-Fe2O3/HZSM-5 catalyst as compared with the O-2+CH4 reaction.

Synthesis and characterization of gallium-based perovskite-type dense membrane with oxygen semipermeability

La0.15Sr0.85Ga0.3Fe0.7O3-delta (LSGFO) and La0.15Sr0.85Co0.3Fe0.7O3-delta (LSCFO) mixed oxygen-ion and electron conducting oxides were synthesized by using a combined EDTA and citrate complexing method, and the corresponding dense membranes were fabricated. The properties of the oxide powders and membranes were characterized with combined SEM, XRD, H-2-TPR, O-2-TPD techniques, mechanical strength and oxygen permeation measurement. The results showed that LSGFO had much higher thermochemical stability than LSCFO due to the higher valence stability of Ga3+. After the temperature-programmed reduction by 5% H-2 in Ar from 20 degreesC to 1020 degreesC, the basic perovskite structure of LSGFO was successfully preserved. LSGFO also favors the oxygen vacancy formation better than LSCFO. Oxygen permeation measurement demonstrated that LSGFO had higher oxygen permeation flux than LSCFO, but they had similar activation energy for oxygen transportation, with a value of 110 and 117 kJ . mol(-1), respectively The difference in oxygen permeation fluxes was correlated with the difference in oxygen vacancy concentrations for the two materials.

Métodos para estimativa de áreas de preservação permanente nas margens dos cursos d'água em grandes bacias: avaliação para a bacia do Rio Ji-Paraná, RO.

O Código Florestal brasileiro, juntamente com a resolução Conama no 303/2002, definiu áreas do território nacional classificadas como de preservação permanente (APP). Essas áreas englobam margens dos cursos e corpos d'água, terrenos com declividade acentuada, bordas de chapadas, topos de morro, entre outras feições. No entanto, a escassez de dados cartográficos em escala adequada e de abrangência nacional dificultam ou até impossibilitam as estimativas do alcance territorial da legislação ambiental brasileira. Um exemplo é a delimitação das APPs nas margens dos rios, que, para identificação correta, requer, além da localização, informações sobre a largura dos cursos d'água na época de cheias, dados raramente disponíveis. Este trabalho utilizou dados provenientes da Agência Nacional de Águas (ANA) para estimar as APPs das margens dos rios pertencentes à bacia do Rio Ji-Paraná, RO, identificados na escala 1:1.000.000, levando-se em consideração as larguras dos cursos d'água. Dados de todas as dez estações fluviométricas presentes na bacia com medidas de cota e perfil transversal da calha foram utilizados para estimar a largura máxima do canal de duas maneiras distintas. A primeira delimitou as sub-bacias definidas pelas estações fluviométricas e considerou que todos os cursos d'água pertencentes à sub-bacia apresentavam a mesma largura observada em seu ponto final. A segunda utilizou a relação empírica obtida entre a área de drenagem e a largura da calha nas nove estações para definir a largura de todos os trechos dos cursos d'água da bacia. Por fim, as APPs nas margens dos rios foram delimitadas seguindo os critérios estabelecidos na resolução Conama no 303/2002. A título de comparação, foram também delimitadas as APPs utilizando larguras constantes de 100 m, 200 m e 500 m de faixa marginal para toda a bacia. Entre os diferentes métodos utilizados, a APP nas margens dos rios variou de 1.541 km2 a 15.876 km2 (2,04% a 21,04% da área da bacia, respectivamente). A grande variação na delimitação das áreas marginais deixa claro que estimativas efetuadas para grandes regiões estarão sempre sujeitas a incertezas, de acordo com os métodos utilizados, e que, portanto, é imprescindível o detalhamento dos procedimentos efetuados para esclarecer as vantagens e limitações a que tais estimativas estão sujeitas.

In situ high temperature X-ray diffraction studies of mixed ionic and electronic conducting perovskite-type membranes

Phase structure and stability of three typical mixed ionic and electronic conducting perovskite-type membranes, SrCo0.8Fe0.2O3-delta (SCF), Ba0.5Sr0.5Co0.8Fe0.2O3-delta (BSCF) and BaCo0.4Fe0.4Zr0.2O3-delta (BCFZ) were studied by in situ high temperature X-ray diffraction at temperatures from 303 to 1273 K and under different atmospheres (air, 2% O-2 in Ar and pure Ar) at 1173 K. By analyzing their lattice parameters the thermal expansion coefficients (TECs) of BSCF, SCF and BCZF are obtained to be 11.5 x 10(-6) K-1, 17.9 x 10(-6) K-1 and 10.3 x 10(-6) K-1, respectively. A relationship between phase stability and TEC was proposed: the higher is the TEC, the lower is the operation stability of the perovskite materials. (C) 2005 Elsevier B.V. All rights reserved.