甘蓝型油菜双低显性细胞核+细胞质雄性不育系DGCMS-3A的构建及遗传模式研究

 【目的】验证显性核不育两用系与波里马三系的基因型,明确Gd1AB和D3AB显性核不育的遗传模式,并构建显性细胞核+细胞质不育系统。【方法】通过显性核三系与波里马三系相互杂交验证其基因型,分析Mf和Rfc基因的等位性,采用临保系与显性纯合两用系×显性核不育恢复系F2代核不育株测交的方法,推论显性纯合两用系Gd1AB和D3AB的遗传控制模式。C3B为轮回父本与不育胞质的显性核不育株定向回交,以创建显性核不育+细胞质不育。【结果】鉴别了Gd1AB和D3AB的遗传控制模式,确定甘蓝型油菜显性纯合两用系Gd1AB由一对复等位遗传模式控制,而显性纯合两用系D3AB由两对基因互作控制。初步构建出双低显性杂合核不育+细胞质不育系统DGCMS-3A,并证实了选育显性纯合核不育+细胞质不育系的可行性。【结论】显性抑制基因Mf与波里马恢复基因Rfc不等位,Gd1AB的基因型为N（MsMsrfcrfc）×N（MsMfrfcrfc）),D3AB的基因型为N（MsMsmfmfrfcrfc）×N（MsMsMfmfrfcrfc）。显性核不育+细胞质不育可细分为四种遗传模式：双位点互作显性杂合核不育+细胞质不育[S（Msmsmfmfrfcrfc）+S（msmsmfmfrfcrfc）]、单位点复等位显性杂合核不育+细胞质不育[S（Msmfrfcrfc）+S（mfmfrfcrfc）]、双位点互作显性纯合核不育+细胞质不育[S（MsMsmfmfrfcrfc）+S（MsMsMfmfrfcrfc）]、单位点复等位显性纯合核不育+细胞质不育[S（MsMsrfcrfc）+S（MsMfrfcrfc）]。     

Identification of a blue photoluminescent composite material from a combinatorial library

A quaternary combinatorial masking strategy was used in conjunction with photolithography to generate compositionally diverse thin-film phosphor libraries containing 1024 different compositions on substrates 2.5 centimeters square. A parallel imaging system and scanning spectrophotometer were used to identify and characterize compositions in the library with interesting luminescent behavior. Optimal compositions were identified with the use of gradient libraries, in which the stoichiometry of a material was varied continuously. This process led to the identification of an efficient blue photoluminescent composite material, Gd3Ga5O12/SiO2. Experimental evidence suggests that luminescence in this material may arise from interfacial effects between SiO2 and Gd3Ga5O12.     

Ti8C12+-Metallo-Carbohedrenes: A New Class of Molecular Clusters?

During the course of studying the dehydrogenation reactions of hydrocarbons by titanium atoms, ions, and clusters, an exceptionally stable and abundant cluster which contains 8 titaniums and 12 carbons was discovered. "Titration" reactions with ND(3) reveal the uptake of eight molecules, pointing to the fact that the titanium atoms are at exposed positions of similar coordination. A dodecahedral structure of T(h) point group symmetry is proposed to account for the unusual stability of this molecular cluster. The Ti(8)C(12)(+) dodecahedron has 12 pentagonal rings and each of the rings is formed by two titanium and three carbon atoms, where each titanium is bound to three carbons. Based on the model, it is expected that neutral Ti(8)C(12) would be a stable metallo-carbododecahedral molecule and may comprise one member of a new class of molecules, namely metallo-carbohedrenes.     

Quantum solvation of carbonyl sulfide with helium atoms

High-resolution infrared and microwave spectra of He(N)-carbonyl sulfide (He(N)-OCS) clusters with N ranging from 2 to 8 have been detected and unambiguously assigned. The spectra show the formation of a solvation layer beginning with an equatorial "donut" of five helium atoms around the OCS molecule. The cluster moment of inertia increases as a function of N and overshoots the liquid droplet limit for N > 5, implying that even atoms in the first solvation shell are decoupled from the OCS rotation in helium nanodroplets. To the extent that this is due to superfluidity, the results directly explore the microscopic evolution of a phenomenon that is formally macroscopic in nature.     

Anomalous scattering study of the bi distribution in the 2212 superconductor: implications for cu valency

The distribution of the bismuth atoms over the cation sites in the 2212 Bi-Sr-Ca-Cu-O superconductor has been determined by anomalous scattering synchrotron crystallography. The analysis of reflection pairs measured at wavelengths of 0.9243 and 0.9600 angstrom shows a delocalization of the bismuth atoms over the calcium and strontium sites. The "mixed" plane between the CuO(2) layers contains 6.0(1.4) percent bismuth (where the number in brackets represents the statistical standard deviation derived from the least-squares refinement of the data), and a much smaller amount of strontium than often assumed. The strontium deficiency is charge-compensated by the creation of electron holes in the CuO(2) layer. The result supports the view that neither extra oxygen nor overlap of the bismuth 6p and copper 3d bands is needed to account for the holes, which are an essential feature of the superconductivity mechanism.     

Imaging surface atomic structure by means of auger electrons

Measurements of the complete angular distribution of Auger electrons emitted from well-defined platinum[111] single-crystal surfaces have led to the discovery that the distributions are composed of "silhouettes" of surface atoms "back lit" by emission from atoms deeper in the solid. Theoretical simulations of Auger electron angular distributions based upon atomic point emitters and spherical atomic scatterers of uniform cross section are in close agreement with these experimental results, but opposite to previous theoretical predictions. In view of the definitive results obtained and the straightforward agreement between theory and experiment, angular distribution Auger microscopy (ADAM) is useful for direct imaging of interfacial structure and investigation of electron-solid interactions in the physical and biological sciences and engineering. Applicability of ADAM is illustrated by images obtained for monolayers of silver and iodine on platinum[111].     

Synthesis of Linear Acetylenic Carbon: The "sp" Carbon Allotrope

A carbon allotrope based on "sp" hybridization containing alternating triple and single bonds (an acetylenic or linear carbon allotrope) has been prepared. Studies of small (8 to 28 carbon atoms) acetylenic carbon model compounds show that such species are quite stable (130 degrees to 140 degrees C) provided that nonreactive terminal groups or end caps (such as tert-butyl or trifluoromethyl) are present to stabilize these molecules against further reactions. In the presence of end capping groups, laser-based synthetic techniques similar to those normally used to generate fullerenes, produce thermally stable acetylenic carbon species capped with trifluoromethyl or nitrile groups with chain lengths in excess of 300 carbon atoms. Under these conditions, only a negligible quantity of fullerenes is produced. Acetylenic carbon compounds are not particularly moisture or oxygen sensitive but are moderately light sensitive.     

The manganese site of the photosynthetic water-splitting enzyme

As the originator of the oxygen in our atmosphere, the photosynthetic water-splitting enzyme of chloroplasts is vital for aerobic life on the earth. It has a manganese cluster at its active site, but it is poorly understood at the molecular level. Polarized synchrotron radiation was used to examine the x-ray absorption of manganese in oriented chloroplasts. The manganese site, in the "resting" (S1) state, is an asymmetric cluster, which probably contains four manganese atoms, with interatomic separations of 2.7 and 3.3 angstroms; the vector formed by the 3.3-angstrom manganese pair is oriented perpendicular to the membrane plane. Comparisons with model compounds suggest that the cluster contains bridging oxide or hydroxide ligands connecting the manganese atoms, perhaps with carboxylate bridges connecting the 3.3-angstrom manganese pair.     

Chemical cartography: finding the keys to the kinetic labyrinth

Very high resolution lasers allow spectroscopic pictures to be taken following a collision between two molecular reactants. The features of these "pictures" are the electronic, vibrational, rotational, and translational motions of the atomic particles, which relate the quantum states of the reactants to the quantum states of the products. Such state-to-state kinetic information can be used to test the shape and nature of the interaction potential that controls the collision process. The potential itself is akin to a map of the terrain through mountains and valleys where elevation is a measure of energy instead of height. Accurate mapping of this potential surface leads to an understanding of the forces which control rates and mechanisms of chemical reactions. The application of four different advanced laser techniques to the study of collisions between "hot" hydrogen(H) atoms and carbon dioxide(CO(2)) molecules has provided a wealth of information about both reactive and nonreactive collisions for this system. The availability of data for rotationally, vibrationally, and translationally inelastic excitation of CO(2) by H atoms, when compared with data for reactive events producing OH + CO, provides insights into the dynamics of collisions between H and CO(2), and illustrates the future promise of these powerful techniques for elucidating features of potential energy surfaces.     

Images of Io's Sodium Cloud

The first direct images of Io's sodium cloud are reported and analyzed. The observed cloud extends for more than 10(5) kilometers along Io's orbit and is a somewhat "banana-shaped" partial toroid. More sodium atoms precede Io than follow it. A model based on the escape of sodium from a specific localized area on Io provides a reasonable fit to the observed intensity distribution whereas isotropic escape does not.     

Theoretical evidence for a c60 "window" mechanism

On the basis of semiempirical and high-level ab initio calculations, theoretical evidence is presented of a "window" mechanism operable on the surface of C(60) and other fullerenes. Through this mechanism, large holes may be formed in fullerenes excited to their triplet state, openings through which atoms and small molecules can pass. This work provides a theoretical foundation for experiments that have prepared endohedral noble gas compounds of C(60) under thermal excitation. A method is proposed that could increase the efficiency of the process of noble gas insertion into C(60) and provide a more general means to create endohedral fullerene compounds.     

Coupled quantum dots fabricated by cleaved edge overgrowth: from artificial atoms to molecules

Atomically precise quantum dots of mesoscopic size have been fabricated in the gallium arsenide-aluminum gallium arsenide material system by cleaved edge overgrowth, with a high degree of control over shape, composition, and position. The formation of bonding and antibonding states between two such "artificial atoms" was studied as a function of quantum dot separation by microscopic photoluminescence (PL) spectroscopy. The coupling strength within these "artificial molecules" is characterized by a systematic dependence of the separation of the bonding and antibonding levels, and of the PL linewidth, on the "interatomic" distance. This model system opens new insights into the physics of coupled quantum objects.     

Quantum confinement and host/guest chemistry: probing a new dimension

Nanoparticulate metals and semiconductors that have atomic arrangements at the interface of molecular clusters and "infinite" solid-state arrays of atoms have distinctive properties determined by the extent of confinement of highly delocalized valence electrons. At this interface, the total number of atoms and the geometrical disposition of each atom can be used to significantly modify the electronic and photonic response of the medium. In addition to teh novel inherent physical properties of the quantum-confined moieties, their "packaging" into nanocomposite bulk materials can be used to define the confinement surface states and environment, intercluster interactions, the quantum-confinement geometry, and the effective charge-carrier density of the bulk. Current approaches for generating nanostructures of conducting materials are briefly reviewed, especially the use of three-dimensional crystalline superlattices as hosts for quantum-confined semiconductor atom arrays (such as quantum wires and dots) with controlled inter-quantum-structure tunneling.     

The active site of methanol synthesis over Cu/ZnO/Al2O3 industrial catalysts

One of the main stumbling blocks in developing rational design strategies for heterogeneous catalysis is that the complexity of the catalysts impairs efforts to characterize their active sites. We show how to identify the crucial atomic structure motif for the industrial Cu/ZnO/Al(2)O(3) methanol synthesis catalyst by using a combination of experimental evidence from bulk, surface-sensitive, and imaging methods collected on real high-performance catalytic systems in combination with density functional theory calculations. The active site consists of Cu steps decorated with Zn atoms, all stabilized by a series of well-defined bulk defects and surface species that need to be present jointly for the system to work.     

2种来源绿玉树夏季乳汁中碳氢化合物和甾醇的气相色谱质谱分析

采用气相色谱-质谱计算机联用技术分析了栽培在重庆的荷兰和海南绿玉树夏季乳汁的碳氢化合物和甾醇的相对含量．结果表明：海南绿玉树乳汁中9～44个碳原子的链烷的总相对含量为8.55%,羊毛甾醇为62.76%,此外,还含有14.32%的酯类和6.07%硫．荷兰绿玉树乳汁中含18～32个碳原子的链烷的总相对含量为2.91%,羊毛甾醇为72.61%,还有11.42%的酯类和6.02%的硫．     

Escape of hydrogen from venus

Recombination of O(2)(+) represents a source of fast oxygen atoms in Venus' exosphere, and subsequent collisions of oxygen atoms with hydrogen atoms lead to escape of about 10(7) hydrogen atoms per square centimeter per second. Escape of deuterium atoms is negligible, and the ratio of deuterium to hydrogen should increase with time. It is suggested that the mass-2 ion observed by Pioneer Venus is D(+), which implies a ratio of deuterium to hydrogen in the contemporary atmosphere of about 10(-2), an initial ratio of 5 x 10(-5) and an original H(2)O abundance not less than 800 grams per square centimeter.     

QUANTUM COMPUTING: Quantum Entangled Bits Step Closer to IT

In contrast to today's computers, quantum computers and information technologies may in future be able to store and transmit information not only in the state "0" or "1," but also in superpositions of the two; information will then be stored and transmitted in entangled quantum states. Zeilinger discusses recent advances toward using this principle for quantum cryptography and highlights studies into the entanglement (or controlled superposition) of several photons, atoms, or ions.     

Conformation of macromolecules in the gas phase: use of matrix-assisted laser desorption methods in ion chromatography

Conformational data for macromolecules in the gas phase have been obtained by the coupling of a matrix-assisted laser desorption ion source to an ion chromatograph. A series of polyethylene glycol (PEG) polymers "cationized" (converted to a cation) by sodium ions (Na(+)PEG9 to Na(+)PEG19) and a protonated neurotransmitter protein, bradykinin, were studied. Mobilities of Na(+)PEG9 to Na(+)PEG19 are reported. Detailed modeling of Na(+)PEG9 with molecular mechanics methods indicates that the lowest energy structure has the Na(+) ion "solvated" by the polymer chain with seven oxygen atoms as nearest neighbors. The agreement between the model and experiment is within 1 percent for Na(+)PEG9, Na(+)PEG13, and Na(+)PEG17, giving strong support to both the method and the deduced structures. Similar agreement was obtained in initial studies that modeled experimental data for arginine-protonated bradykinin.