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C12H12I2Te4, M(r) = 920.44, monoclinic, P2(1)/n, a = 10.942 (2), b = 14.924 (2), c = 11.415 (2) angstrom, beta = 104.32 (1)-degrees, V = 1806.0 (5) angstrom 3, Z = 4, D(x) = 3.38 g cm-3, lambda(Mo K-alpha) = 0.71069 angstrom, mu = 100.7 cm-1, F(000) = 1592, T = 294 K, R = 0.033 for 1828 observed reflections. One of the Te atoms is bonded to the two I atoms, which are on either side of the molecular plane. The Te-I distances are 2.963 (1) and 2.961 (1) angstrom, which means oxidation at the Te atom instead of at the C = C bonds.

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A hydrodynamic-thermodynamic equation set was set up to reflect the formational mechanism and evolution of the Northern Yellow (Huanghai) Sea cold water mass (NYSCWM) and its density circulation. Appropriate mathematical physical models were established by using some physical postulations. An approximate analytic solution to expound the distributions of temperature and three-dimensional current velocity, which can be used to expound the formational mechanism of the NYSCWM and its density circulation is obtained by using the theory of boundary layer and perturbational analyses.

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能量代谢指动物在进行生理活动(如摄食、消化以及动物的活动等)时所消耗能量的总和,一般以动物的呼吸率利排泄率来估计动物的能量代谢。其主要研究内容是闸明生物能量代谢的基木规律以及与环境闪子的关系。菲律宾蛤仔(Ruditapesphil ippmarum)是我国一种重要的养殖贝类,关于其能量代谢的研究却较少,这种状况妨碍了菲律宾蛤仔养殖生态理论的完善和养殖技术的提高。本研究主要对菲律宾蛤仔呼吸率和排泄率的基本规律(能量代谢与体重的关系、能量代谢的昼夜变化)及其与环境因子(饵料浓度、水温、栖息底质环境)的关系进行探讨。研究结果如下:1.不同体重菲律宾蛤仔代谢率小同。实验川菲律宾蛤仔分三种大小:l(干肉重为0.07-0.14g)、ll(干肉重0.27-0.34g)、III(干肉重0.45~0.63g)。温度包括:26℃(八月)、20℃(十月)、1 5℃(十二月)、9℃(一月)。实验共设四个饵料浓度:2.28±0.25,6.454±0.44,10.284±0.82,15.414±1.56mgTPM/L(TPM,总颗粒物),饵料中POM(颗粒有机物)含量都为4.68±1.64 mg/L。常温下菲律宾蛤仔代谢率随着体重的增大而增大。15℃、20~C、26℃时蛤仔呼吸率与干肉重呈明显的幂函数关系R=aW~b,a值变动范围为0.1076-0.3309;b值变动范围为0.239l~0.8381;蛤仔排泄率与干肉重也呈明显的幂函数关系N=aW~b,a值变动范围为14.213~68.362:b值变动范围为0.3673-1.1 532。9℃(饵料浓度为2.28±0.25mgTPM/L)、20℃(饵料浓度为10.284-0.82mgTPM/L)、26℃(饵料浓度为6.454±0.44mgTPM/L)时不同体重蛤仔氧氮比差异显著,其它情况下不同体重蛤仔氧氮比差异不显著。2.常温下菲律宾蛤仔代谢率受饵料浓度的影响,不同大小蛤仔受饵料浓度的影响程度不同。I组蛤仔呼吸率受饵料浓度的显著影响,II组III组蛤仔呼吸率只在9℃(一月)和26~C(八月)时受饵料浓度的显著影响。26℃时影响最显著,26℃时I组蛤仔在饵料浓度为2.28±0.25,6.45±0.44,l0.28±0.82,15.4l±1.56mgTPM/L时呼吸率分别是O.086,0.146,0.073,0.093(mlO_2/h);ll组蛤仔在上述浓度饵料中呼吸率分别是0.138,0.214,0.J 26,0.12l(mlO_2/h);III组蛤仔在上述浓度饵料中呼吸率分别是0.129,0.266,0.186,0.192(mlO_2/h)。菲律宾蛤仔呼吸率在饵料浓度为6.45±0.44 mgTPM/L时最高,蛤仔呼吸率在其它饵料浓度时都会降低。菲律宾蛤仔排泄率在饵料浓度为10.28±0.82 mgTPM/L和15.4l士1.56mgTPM/L时显著高于其它浓度组,9℃时这种趋势更明显,9℃时饵料浓度为2.28±0.25,6.454±044,lO.284±0.82,15.41±1.56mgTPM/L中I组蛤仔排泄率分别是4.297,2.874,8.003,6.658(μgNH_3-N/h);II组蛤仔在上述浓度饵料中排泄率分别是4.011,3.609,10.427,12.732(μgNH_3-N/h);III组蛤仔在上述浓度饵料中排泄率分别是2.28 l,6.452,10.283,15.417(μgNH_3-N/h)。3.菲律宾蛤仔代谢率受自然温度的显著影Ⅱ向。I组蛤仔在9℃、15℃、20℃、26℃时呼吸率平均为0.057,0.085,0.039,O.099;II组蛤仔在上述四个温度中呼吸率平均为0.08,O.128,0.089,0.149(mlO_2/h),I组和II组蛤仔在9℃和20~C时呼吸率较低,在26℃时呼吸率最高。III组蛤仔在上述四个温度中呼吸率平均为0.09,O.1 59,O.143,O.193(mlO_2/h),在9℃时llI组蛤仔呼吸率显著低于其它温度组。温度为9℃、15℃、20℃、26℃时l组蛤仔排泄率平均为5.458,13.169,4.946,11.138(μgNH_3-N/h):II组蛤仔在上述温度中排泄率平均为7.695,23.578,8.319,23.90l(μgNH_3-N/h);III组蛤仔在上述温度中排泄率平均为11.738,27.443,15.658,35.407(μgNH_3-N/h),蛤仔排泄率在15℃和26℃时均高于9℃和20℃。4.摄食状态与饥饿状态菲律宾蛤仔代谢率有明显不同。26℃时蛤仔静止状态呼吸率平均为0.336(m102/g干重.h),摄食状态呼吸率平均为0.656(ml0_2干重.h),摄食状态呼吸率比静止状态平均升高了0 32(ml0_2/g干重.h);26℃时蛤仔静止状态排泄率平均为39.471(μgNH_3-N/g干重.h),摄食状态排泄率平均为88.08(μgNH_3-N/g干重.h),摄食状态排泄率比静止状态排泄率平均升高了48.6(μgNH_3-N/g干重.h)。摄食状态代谢率平均是静止状态的2~3倍。根据摄食引起的呼吸率和排泄率升高量得出每氧化产生lμgNH_3-N需0_2量平均为7.05μl。5.人工控制温度对菲律宾蛤仔代谢率有明显影响。不同大小蛤仔受温度的影响程度不同。在温度5℃、10℃、l 5℃、20℃、26℃,I组和II组蛤仔呼吸率都随着温度的升高而升高,在10℃~l5℃和20℃~26℃这二个温度变化范围内呼吸率变化最大,在20℃~26℃时I组蛤仔呼吸率变动范围为O.85~1.04(m10_2/g干重.h)、II组蛤仔变动范围为0.57~0.86(ml0_2/g干重.h)。III组蛤仔呼吸率只在5℃~l0℃时明显增高,变动范围为0.09~0.5l(m10_2/g干重.h),在10℃~26℃范围内变化不大。I组和II组蛤仔排泄率随着温度的升高而升高,变动幅度较大,在5℃~26℃范围内其排泄率变动范围为10.32~81.53(μgNH_3-N/g干重.h);而 III组蛤仔排泄率只在5℃~15℃时随着温度的升高而升高,其排泄率变动范围为6.75~23.77(μgNH_3-N/g干重.h),在15℃~26℃范围内几乎不变。III组蛤仔的适温范围比I组和II组蛤仔广。菲律宾蛤仔在5℃和10℃时氧氮比变化明显,变动范围为2.76~11.44,在15~26℃时变化不大。6.菲律宾蛤仔代谢率有明显的日节律性,呈正弦曲线型变化。蛤仔夜问代谢率明显升高。I组蛤仔夜间呼吸率平均为0.867(m10_2/g干重.h),白天呼吸率平均为O.504(m10_2/g干重.h);II组蛤仔夜间呼吸率平均为0.438(m10_2/g干重.h),白天呼吸率平均为0.36l(m102/g干重.h);III组蛤仔夜间呼吸率平均为0.409(m10_2/g干重.h),白天呼吸率平均为0.252(m102/g干重.h)。在22:00-23:00菲律宾蛤仔呼吸率最高。7.底质环境对菲律宾蛤仔的代谢率有明显影响。在饥饿状态下菲律宾蛤仔在泥沙底质中呼吸率平均为l 406(m10_2/g干重h),在无泥沙环境中呼吸率平均为O.963(ml0_2/g干重.h);摄食状态下菲律宾蛤仔在泥沙底质中呼吸率平均为1.59l(m102/g干重.h),在无泥沙环境中呼吸率平均为1.115(m10_2/g干重.h)。在饥饿状态下菲律宾蛤仔在泥沙底质中排泄率平均为78.934(μgNH_3-N/g 干重.h),在无泥沙环境巾排泄率平均为45.043(μgNH_3-N/g干重.h);摄食状态下菲律宾蛤仔在泥沙底质中排泄率平均为87.12l(μgNH_3-N/g干重.h),在无泥沙底质中排泄率平均为58.354(μgNH_3-N/g干重.h)。蛤仔在泥沙环境中呼吸率和排泄率都明显升高。

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用饱和溶液法制备了二茂铁酰腙类化合物乙酰基二茂铁呋喃甲酰腙(A FH) 与β-环糊精的包结物。元素分析及溶解常数测定结果证明两者形成了1∶1 包结物.。从溶解度曲线计算得出包合常数为227. 3 L ·mol- 1. 通过UV , FT IR, X 射线粉末衍射研究了包结特性, 并用NMR 技术推断了包结物的结构。

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矾山明矾石矿床位于江山-绍兴深断裂南东侧,海西印支褶皱带的南东侧,中国板块东南构造区与太平洋板块的交接处,属于中国板块东南构造区。该矿床产在矾山破火山口内,是一个超大型明矾石矿床,同时矿床中的钒、镓含量也达到了综合利用的品位。该矿床研究程度低,缺少地球化学特征研究。因此,本次工作系统研究了该矿床常量元素、微量元素、稀土元素、硫和铅同位素地球化学特征。本次对明矾石矿床的研究获得以下几点初步认识: 1:成矿物质来源于火山岩。矿区火山岩中的K、Al、Na等矿石元素含量明显比其他地区高,并且从围岩→矿化围岩→矿石呈明显的富集趋势。稀土资料和铅同位素资料也都表明成矿物质来源于中生代火山岩。 2:V、Ga含量达到了综合利用的品位。微量元素资料表明,矿石中V平均含量为211.6ppm,Ga平均含量为16.78ppm,都大于地壳丰度,尤其是V远大于地壳丰度;同时发现,成矿时V以V¬5+形式通过与Al3+发生类质同像进入明矾石晶格,而矿石中Ga含量除与Al3+外还与Fe3+含量有关。 3:明矾石的稀土元素地球化学特征比较复杂。根据δEu值不同可分为三类: Eu弱负异常型,Eu弱正异常型和Eu强正异常型。影响稀土元素分布的因素主要为成矿原岩中富含碱性长石和成矿时的氧逸度和温度,另外矿石结构(如孔隙度)对稀土元素分布也有影响。研究表明,矿石稀土配分模式为轻稀土富集型,与火山岩基本一致。 4:硫同位素研究发现,黄铁矿的δ34S值为1.9~3.2‰,明矾石的δ34S值为13.62~16.02‰,后者明显大于前者。本次研究认为黄铁矿的δ34S值代表当时的岩浆源硫,而明矾石较大的δ34S值为岩浆硫经过同位素分馏的结果。铅同位素研究发现,明矾石矿石的206Pb/204Pb=17.963~18.606,207Pb/204Pb=15.439~15.672,208Pb/204Pb=38.405~38.796。通过与中生代火山岩和基底变质岩的对比,本次研究认为明矾石的铅源为中生代火山岩来源,与基底变质岩并无直接的来源关系。 5:通过明矾石矿床的地球化学特征研究,结合实际地质特征和前人研究成果,本次研究提出了以下矿床成因:明矾石矿床形成环境为浅成低温氧化环境;成矿物质来源于围岩,成矿所需的硫源为分馏的岩浆硫;矿床形成时期为73~95Ma,比围岩晚10~20Ma;矿床成因为火山热液交代成因。 浙江省中生代火山岩成矿体系主要指受浙江省中生代火山构造、岩浆活动控制的一系列不同类型的矿床组合。成矿体系主要受江绍深断裂带和中生代陆相火山岩控制。前人对成矿体系中的单一矿床研究较多,但是缺少横向对比研究。本次工作主要通过对成矿体系中的两类矿床(金属矿床和非金属矿床)进行对比研究,结合中生代火山岩演化过程,初步探索成矿体系中各类矿床间的联系以及成矿体系与火山岩演变的关系。本次工作取得以下几点初步认识: 1:成矿体系中各类矿床的整体分布受江绍深断裂、温州-镇海大断裂等一些深大断裂控制。各矿床的具体控(容)矿构造都为次级压-压扭性断裂和破火山口构造,其中破火山口构造在成矿过程中占非常重要的作用。 2:成矿体系中各类矿床的成矿温度低,深度浅,为典型的浅成低温矿床。 3:铅同位素资料表明,矿床的铅源为中生代火山岩来源,与基底并无直接联系。氢氧同位素资料表明,各类矿床的成矿流体以中生代大气降水为主,岩浆水占很少部分或并无参与成矿。 4:成矿体系存在明显的成矿成岩时差,金属矿床在12.44~45.6Ma,萤石矿床为25~75Ma,其他非金属矿床为10~20Ma;铅锌(银)金等金属矿床为具有明显的两期成矿特征。

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A avaliacao de cultivares de trigo no Parana, com fins de recomendacao, e realizada pelas Instituicoes: IAPAR, Embrapa Soja, COODETEC e Fundacao Agraria de Pesquisa, atraves da instalacao de ensaios de rendimento nas principais regioes triticolas do Estado. Sao relatados os resultados obtidos em 1996 de 17 experimentos do Ensaio Intermediario Paranaense (IPR), 25 experimentos do Centro-Sul Brasileiro (CSBR) e 24 experimentos do Ensaio em Cultivo (ECR), para solos com aluminio, instalados em Londrina, Faxinal, Campo Mourao, Cascavel, Pato Branco, Arapoti, Tibagi, Ponta Grossa e Guarapuava, representando as regioes Norte, Oeste, Sudoeste e Sul do Estado. Os rendimentos dos ensaios instalados em Faxinal foram prejudicados por chuva de granizo. Devido a pouca precipitação, os ensaio instalados em Londrina e Cascavel receberam irrigacao, para assegurar a emergencia uniforme das plantas. A ocorrencia de doencas foi muito baixa, principalmente nas regioes Norte e Oeste. No Sul e Sudoeste, onde a precipitacao foi mais elevada, ocorreu maior incidencia de doencas fungicas e os pesos do hectolitro foram menores. Em alguns experimentos obteve-se produtividade media superior a 5 t/ha, considerada elevada para o trigo. No ensaio IPR, foram promovidas, em funcao do rendimento e outras caracteristicas, as linhagens OC 962, OC 963, OC 968, ORL 93320, PF 90120 e PF 9293. No CSBR, destacaram-se e foram mantidas as linhagens OC 959, OC 9511, ORL 9285, PF 9099, PF 91205 e PG 9337. No ECR, destacaram-se, em mais de uma regiao, as cultivares EMBRAPA-27, OR 1, IAPAR 46, IAPAR 60, IAPAR 78 e T. BR 23.

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O estado do Parana apresenta uma diversidade de clima, com invernos irregulares em relacao a precipitacoes pluviometricas e ocorrencia de geadas, e tambem, com relacao aos tipos de solos, que influem na adaptacao e no desempenho dos genotipos de trigo. Em vista disto, ha necessidade de um maior numero de cultivares, com caracteristicas diferenciadas para serem utilizadas pelos produtores. O presente trabalho tem por objetivo avaliar, nas zonas A e B, em solos com ate 5% de saturacao de aluminio, os novos genotipos de trigo criados pelas diferentes instituicoes que desenvolvem trabalhos de melhoramento genetico de trigo. Esta avaliacao e realizada pelo Instituto Agronomico do Parana (IAPAR), pelo Centro Nacional de Pesquisa de Soja (Embrapa Soja) e pela Cooperativa Central de Desenvolvimento Tecnologico e Economico (COODETEC), atraves da instalacao de diferentes ensaios de competicao de genotipos. Os resultados aqui relatados sao resultantes de dez experimentos do Ensaio Intermediario Paranaense (IPS), doze experimentos do Ensaio Centro-Sul Brasileiro (CSBS) e onze experimentos do Ensaio de Cultivares em Cultivo (ECS), para solos com ate 5% de saturacao de aluminio, instalados em 1996, em diferentes epocas, nas localidade de Cambara, Londrina, Engenheiro Beltrao, Palotina e Sao Miguel do Iguacu. Devido a longa estiagem ocorrida no periodo de abril a julho, no Norte do estado (zona A1), alguns experimentos foram prejudicados e, outros perdidos. Em Londrina e Palotina, os experimentos receberam irrigacoes na fase inicial para propiciar uma boa germinacao e desenvolvimento das plantas. A incidencia de molestias foi baixa, em ambas as zonas predominando no entanto, uma razoavel infeccao de oidio, nas semeaduras mais tardias, e de ferrugem da folha. Observou-se uma variabilidade dos genotipos quanto ao grau de tolerancia e/ou suscetibilidade a estas molestias, como tambem, uma resposta no rendimento de graos ao controle destas, pelo uso de fungicidas especificos. Os rendimentos obtidos, em geral, foram muitos bons, alcancando, em alguns casos, a 6,7 t/ha. No ensaio IPS, em funcao do rendimento de graos e outras caracteristicas, foram selecionadas as linhagens IA 952, IWT 9430, LD 941, LD 946, OC 962, OC 963, OC 965, ORL 92203 e PR 961. NO CSBS, foram mantidas as linhagens IOR 90226 e PF 91450. No ECS, destacaram-se, em ambas as zonas, as cultivares IAPAR 60, IAPAR 78 e OR 1. Considerando os resultados de rendimentos de graos e outras caracteristicas agronomicas e, principalmente, a qualidade da farinha para panificacao, foram recomendadas como novas cultivares, as linhagens IDS 934-21 e OC 939, denominadas, respectivamente, de Manitoba 97 e COODETEC 101.

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Edkins Jenny, 'The Criminalisation of Mass Starvations: From Natural Disaster to Crime Against Humanity', In: 'The New Famines: Why Famines Persist in an Era of Globalisation', (New York: Routledge), pp.50-65, 2006 RAE2008

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Russell M. Morphew, Hazel A. Wright, E. James LaCourse, Debra J. Woods and Peter M. Brophy (2007). Comparative proteomics of excretory-secretory proteins released by the liver fluke Fasciola hepatica in sheep host bile and during in vitro culture ex host. Molecular and Cellular Proteomics, 6 (6), 963-972. Sponsorship: BBSRC / EU RAE2008

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In this thesis we relate the formal description of various cold atomic systems in the energy eigenbasis, to the observable spatial mode dynamics. Herein the `spatial mode dynamics' refers to the direction of photon emission following the spontaneous emission of an excited fermion in the presence of a same species and spin ideal anisotropic Fermi sea in its internal ground state. Due to the Pauli principle, the presence of the ground state Fermi sea renders the phase space, anisotropic and only partially accessible, thereby a ecting the direction of photon emission following spontaneous emission. The spatial and energetic mode dynamics also refers to the quantum `tunneling' interaction between localised spatial modes, synonymous with double well type potentials. Here we relate the dynamics of the wavefunction in both the energetic and spatial representations. Using this approach we approximate the relationship between the spatial and energetic representations of a wavefunction spanning three spatial and energetic modes. This is extended to a process known as Spatial Adiabatic Passage, which is a technique to transport matter waves between localised spatial modes. This approach allows us to interpret the transport of matter waves as a signature of a geometric phase acquired by the one of the internal energy eigenstates of the system during the cyclical evolution. We further show that this geometric phase may be used to create spatial mode qubit and qutrit states.

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En este artículo, presento las ideas del profesor Ubiratan D’Ambrosio sobre la Etnomatemática, sus objetivos, su metodología, la relación entre Etnomatemática y Educación Matemática, la enseñanza de las matemáticas en aulas multiculturales, y sus comentarios sobre una caracterización de los trabajos de investigación en Etnomatemática realizados en Colombia. Caracterización publicada en: Blanco, H. La Etnomatemática en Colombia. Un programa en construcción. BOLEMA, año 19, No. 26. 2006. Esta entrevista fue realizada el sábado, 20 de marzo de 2004 en el VI Congreso de Historia de las Ciencias y la Tecnología. Buenos Aires, Argentina.

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In recent history, a number of tragic events have borne a consistent message; the social structures that existed prior to and during the evacuation significantly affected the decisions made and the actions adopted by the evacuating population in response to the emergency. This type of influence over behaviour has long been neglected in the modelling community. This paper is an attempt to introduce some of these considerations into evacuation models and to demonstrate their impact. To represent this type of behaviour within evacuation models a mechanism to represent the membership and position within social hierarchies is established. In addition, individuals within the social groupings are given the capacity to communicate relevant pieces of data such as the need to evacuate—impacting the response time—and the location of viable exits—impacting route selection. Furthermore, the perception and response to this information is also affected by the social circumstances in which individuals find themselves. Copyright © 2005 John Wiley & Sons, Ltd.