Reactions of copper(I) aryloxides with phenyl isothiocyanate: steric and ligand control in the oligomerization of [N-phenylimino(aryloxy)methanethiolato]copper(I) complexes

The preparation of five different copper(I) complexes [CuSC(=NPh)(OAr)}L(n)]m (1-5) formed by the insertion of PhNCS into the Cu-OAr bond and the crystal structure analyses of three of them have been carried out. A monomeric species 1 (OAr = 2,6-dimethylphenoxide) is formed in the presence of excess PPh3 (n = 2, m = 1) and crystallizes as triclinic crystals with a = 12.419(4) angstrom, b = 13.298(7) angstrom, c = 15.936(3) angstrom, alpha = 67.09(3)-degrees, beta = 81.63(2)-degrees, gamma = 66.54(3)-degrees, V = 2224(2) angstrom3, and Z = 2. The structure was refined by the least-squares method to final R and R(w) values of 0.038 and 0.044, respectively, for 7186 unique reflections. Copper(I) 2,5-di-tert-butyl-4-methylphenoxide results in the formation of a dimeric species 2 in the presence of P(OMe)3 (n = 1, m = 2), where the coordination around Cu is trigonal. Crystals of 2 were found to be orthorhombic with a = 15.691(2) angstrom, b = 18.216(3) angstrom, c = 39.198(5) angstrom, v = 11204(3) angstrom3, and Z = 8. Least-squares refinement gave final residuals of R = 0.05 and R(w) = 0.057 with 6866 unique reflections. A tetrameric species 3 results when PPh3 is replaced by P(OMe)3 in the coordination sphere of copper(I) 2,6-dimethylphenoxide. It crystallizes in the space group P1BAR with a = 11.681 (1) angstrom, b = 13.373(2) angstrom, c = 20.127(1) angstrom, a = 88.55(l)-degrees, beta = 89.65(l)-degrees, gamma = 69.28(1)-degrees, V = 2940(l) angstrom3, and Z = 2. Least-squares refinement of the structure gave final values of 0.043 and 0.05 for R and R(w) respectively using 12214 unique reflections. In addition, a dimeric species 4 is formed when 1 equiv of PPh3 is added to the copper(I) 4-methylphenoxide, while with an excess of PPh3 a monomeric species 5 is isolated. Some interconversions among these complexes are also reported.

Synthesis, properties and crystal structures of diastereomeric areneruthenium(II) chiral Schiff-base complexes

Diastereomers (SRu,Sc)-1a and (RRu,Sc)-1b, in a ratio of 85: 15 and formulated as [Ru(η-MeC6H4Pri-p)Cl(L*)], have been prepared by treating [{Ru(η-MeC6H4Pri-p)Cl2}2] with the sodium salt of (S)-α-methylbenzylsalicylaldimine (HL*) in tetrahydrofuran at –70 °C. The reaction of 1(1a+1b) with AgClO4 in acetone followed by an addition of PPh3 or 4-methylpyridine (4Me-py) leads to the formation of adducts [Ru(η-MeC6H4Pri-p)(PPh3)(L*)]ClO42[(SRu,Sc)2a, (FRu,Sc)2b] and [Ru(η-MeC6H4Pri-p)(4Me-py)(L*)]ClO43[(SRu,Sc)3a, (RRu,Sc)3b] in the diastereomeric ratios (SRu,Sc) : (RRu,Sc) of 2 : 98 and 76 : 24, respectively. Complex 1 crystallises with equal numbers of 1a and 1b molecules in an asymmetric unit of monoclinic space group P21 with a= 10.854(1), b= 17.090(1), c= 12.808(4)Å, β= 110.51(1)°, and Z= 4. The structure was refined to R= 0.0552 and R′= 0.0530 with 2893 reflections having I[gt-or-equal] 1.5σ(I). The absolute configurations of the chiral centres in the optically pure single crystal of the PPh3 adduct have been obtained from an X-ray study. Crystals of formulation [Ru(η-MeC6H4Pri-p)-(PPh3)(L*)]2[ClO4][PF6]·1.5 CHCl3, obtained in presence of both ClO4 and PF6 anions, belong to the non-centric triclinic space group P1 with a= 10.852(2), b= 14.028(1), c= 15.950(2)Å, α= 91.51(1), β= 105.97(1), γ= 106.11(1)°, and Z= 2. The final residuals were R= 0.0713, R′= 0.0752 with 7283 reflections having I[gt-or-equal] 2.5σ(I). The crystal structures of 1a,1b, and the PPh3 adduct (2b,2b′) consist of a ruthenium(II) centre bonded to a η-p-cymene, a bidentate chelating Schiff base, and a unidentate ligand (Cl or PPh3). The chirooptical properties of the complexes have been studied using 1H NMR and CD spectral data. The presence of a low-energy barrier for the intermediate involved in these reactions, showing both retention as well as inversion of the metal configuration, is discussed.

Organometallic Chemistry of Diphosphazanes. 11. Reactions of fac-[Mo(CO)3(MeCN){.eta.2-Ph2PN(Pri)PPh(DMP)}] (DMP = 3,5-Dimethyl-1-Pyrazolyl) with Diphosphazanes and Diphosphinoalkanes and Oxidative Addition with Iodine

The use of fac-[Mo(CO)(3)(MeCN)(eta(2)-L(1))] (1a) {L(1) = Ph(2)PN(Pr-i)PPh(DMP)}(2) as a precursor to metalloligands and bimetallic, heterotrimetallic, and heptacoordinated complexes is reported. The reaction of 1a with diphosphazane, dppa, or a diphosphinoalkane such as dppm or dppe yields the fac-eta(1)-diphosphine substituted metalloligands, fac-[Mo(CO)(3)(eta(2)-L(1))(eta(1)-PXP)] {PXP = dppa (2), dppm (3), and dppe (4)}. These undergo isomerization to yield the corresponding mer-diphosphine complexes (5-7). Oxidation of the uncoordinated phosphorus atom of the mer-eta(1)-dppm-substituted complex eventually provides mer-[Mo(CO)(3)-(eta(2)-L(1)){eta(1)-Ph(2)PCH(2)P(O)Ph(2)}](8). The structure of the latter complex has been confirmed by single crystal X-ray diffraction {triclinic system, P ($) over bar 1; a = 11.994(3), b = 14.807(2), c = 15.855(3) Angstrom; alpha = 114.24(1), beta = 91.35(2), and gamma = 98.95(1)degrees; Z = 2, 4014 data (F-0 > 5 sigma(F-0)), R = 0.066, R(W) = 0.069}. Treatment of the dppe metalloligand 7 with [PtCl2(COD)] yields the heterotrimetallic complex cis-[PtCl2{mer-[Mo(CO)(3)(eta(2)-L(1))(eta(1)-dppe]}(2)] (9). Attempts to prepare a related trimetallic complex with the dppm-containing metalloligand were unsuccessful; only the tetracarbonyl complex cis-[Mo(CO)(4)(eta(2)-L(1))] (1b) and cis-[PtCl2(eta(2)-dppm)] were obtained. Reaction of la with dppe in the ratio 2:1 yields the mer-mer dinuclear complex [{mer-[Mo(CO)(3)(eta(2)-L(1))]}(2)(mu-dppe)] (10) bridged by dppe. Oxidation of 1a with iodine yields the Mo(II) heptacoordinated complex [MoI2(CO)(2)(eta(3)-L(1))] (11) with tridentate PPN coordination. The same Mo(II) complex 11 is also obtained by the direct oxidation of the tetracarbonyl complex cis-[Mo(CO)(4)(eta(2)-L(1))] (1b) with iodine. The structure of 11 has been confirmed by X-ray diffraction studies {monoclinic system, Cc; a = 10.471(2), b = 19.305(3), c = 17.325(3) Angstrom; beta = 95.47(2)degrees; Z = 4, 3153 data (F-0 > 5 sigma(F-0)), R = 0.049, R(W) = 0.051}. This complex exhibits an unusual capped-trigonal prismatic geometry around the metal. A similar heptacoordinated complex 12 with a chiral diphosphazane ligand {L(3) = (S,R)-P(h)2PN-(*CHMePh)*PPh(DMP)} has also been synthesized.

Ethyl 6-methyl-2-sulfanylidene-4-[4(trifluoromethyl)phenyl]-1,2,3,4-tetrahyd ropyrimidine-5-carboxylate

The title compound, C(15)H(15)F(3)N(2)O(2)S, adopts a conformation with an intramolecular C-H center dot center dot center dot pi interaction. The dihedral angles between the planes of the 4-(trifluoromethyl) phenyl and ester groups with the plane of the six-membered tetrahydropyrimidine ring are 81.8 (1) and 16.0 (1)degrees, respectively. In the crystal structure, intermolecular N-H center dot center dot center dot S hydrogen bonds link pairs of molecules into dimers and N-H center dot center dot center dot O interactions generate hydrogen-bonded molecular chains along the crystallographic a axis.

(2E)-1-(5-Chlorothiophen-2-yl)-3-(2,3-dimethoxyphenyl)prop-2-en-1-one

In the title compound, C(15)H(13)ClO(3)S, the chlorothiophene and dimethoxyphenyl groups are linked by a prop-2-en-1-one group. The C=C double bond exhibits an E conformation. The molecule is non-planar, with a dihedral angle of 31.12 (5)degrees between the chlorothiophene and dimethoxyphenyl rings. The methoxy group at position 3 is coplanar with the benzene ring to which it is attached, with a C-O-C-C torsion angle of -3.8 (3)degrees. The methoxy group attached at position 2 of the benzene ring is in a (+)synclinal conformation, as indicated by the C-O-C-C torsion angle of -73.6 (2)degrees. In the crystal, two different C-H center dot center dot center dot O intermolecular interactions generate chains of molecules extending along the b axis.

Methyl 2,2-bis(2,4-dinitrophenyl)ethanoate

In the title compound, C(15)H(10)N(4)O(10), the dihedral angle between the aromatic rings is 89.05 (16)degrees. One O atom of one of the nitro groups is disordered over two sites in a 0.70:0.30 ratio. In the crystal, the molecules are linked by weak C-H center dot center dot center dot O interactions.

Structural characterization of backbone-expanded helices in hybrid peptides: (αγ) n and (αβ) n sequences with unconstrained β and γ homologues of L-Val

Learning your αβγ's: The diversity of hydrogen-bonding patterns in backbone-expanded hybrid helices is shown by crystal-structure determination of several oligomeric peptides (see scheme; C=gray; H=white; O=red; N=blue). C 12 helices were observed in the αγ peptide series for n=2-8. In comparison, the αα peptide and αβ peptide sequences show C 10 and mixed C 14/C 15 helices, respectively. Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

A Rodinian suture in western India: New insights on India-Madagascar correlations

We report detailed evidence for a new paleo-suture zone (the Kumta suture) on the western margin of southern India. The c. 15-km-wide, westward dipping suture zone contains garnet-biotite, fuchsite-haematite, chlorite-quartz, quartz-phengite schists, biotite augen gneiss, marble and amphibolite. The isochemical phase diagram estimations and the high-Si phengite composition of quartz-phengite schist suggest a near-peak condition of c. 18 kbar at c. 550 degrees C, followed by near-isothermal decompression. The detrital SHRIMP U-Pb zircon ages from quartz-phengite schist give four age populations ranging from 3280 to 2993 Ma. Phengite from quartz-phengite schist and biotite from garnet-biotite schist have K-Ar metamorphic ages of ca. 1326 and ca. 1385 Ma respectively. Electron microprobe-CHIME ages of in situ zircons in quartz-phengite schist (ca. 3750 Ma and ca. 1697 Ma) are consistent with the above results. The Bondla ultramafic-gabbro complex in the west of the Kumta suture compositionally represents an arc with K-Ar biotite ages from gabbro in the range 1644-1536 Ma. On the eastern side of the suture are weakly deformed and unmetamorphosed shallow westward-dipping sedimentary rocks of the Sirsi shelf, which has the following upward stratigraphy: pebbly quartzite/sandstone, turbidite, magnetite iron formation, and limestone; farther east the lower lying quartzite has an unconformable contact with ca. 2571 Ma quartzo-feldspathic gneisses of the Dharwar block with a ca. 1733 Ma biotite cooling age. To the west of the suture is a c. 60-km-wide Karwar block mainly consisting of tonalite-trondhjemite-granodiorite (TTG) and amphibolite. The TTGs have U-Pb zircon magmatic ages of ca. 3200 Ma with a rare inherited core age of ca. 3601 Ma. The K-Ar biotite cooling age from the TTGs (1746 Ma and 1796 Ma) and amphibolite (ca. 1697 Ma) represents late-stage uplift. Integration of geological, structural and geochronological data from western India and eastern Madagascar suggest diachronous ocean closure during the amalgamation of Rodinia; in the north at around ca. 1380 Ma, and a progression toward the south until ca. 750 Ma. Satellite imagery based regional structural lineaments suggests that the Betsimisaraka suture continues into western India as the Kumta suture and possibly farther south toward a suture in the Coorg area, representing in total a c. 1000 km long Rodinian suture. (C) 2013 Elsevier B.V. All rights reserved.

Dual Stress and Thermally Driven Mechanical Properties of the Same Organic Crystal: 2,6-Dichlorobenzylidene-4-fluoro-3-nitroaniline

An elastic organic crystal, 2,6-dichlorobenzylidine-4-fluoro-3-nitroaniline (DFNA), which also shows thermosalient behavior, is studied. The presence of these two distinct properties in the same crystal is unusual and unprecedented because they follow respectively from isotropy and anisotropy in the crystal packing. Therefore, while both properties lead from the crystal structure, the mechanisms for bending and thermosalience are quite independent of one another. Crystals of the low-temperature (a) form of the title compound are bent easily without any signs of fracture with the application of deforming stress, and this bending is within the elastic limit. The crystal structure of the a-form was determined (P2(1)/c, Z = 4, a = 3.927(7) angstrom, b = 21.98(4) angstrom, c = 15.32(3) angstrom). There is an irreversible phase transition at 138 degrees C of this form to the high-temperature beta-form followed by melting at 140 degrees C. Variable-temperature X-ray powder diffraction was used to investigate the structural changes across the phase transition and, along with an FTIR study, establishes the structure of the beta-form. A possible rationale for strain build-up is given. Thermosalient behavior arises from anisotropic changes in the three unit cell parameters across the phase transition, notably an increase in the b axis parameter from 21.98 to 22.30 angstrom. A rationale is provided for the existence of both elasticity and thermosalience in the same crystal. FTIR studies across the phase transition reveal important mechanistic insights: (i) increased pi...pi repulsions along 100] lead to expansion along the a axis; (ii) change in alignment of C-Cl and NO2 groups result from density changes; and (iii) competition between short-range repulsive (pi...pi) interactions and long-range attractive dipolar interactions (C-Cl and NO2) could lie at the origin of the existence of two distinctive properties.

Influencia de diferentes períodos de destete sobre peso de la hembra al destete (PHD), peso de la camada al destete (PCD) y peso de la hembra al segundo parto (PHP2) en conejas primiparas, en el municipio de Rivas

El presente ensayo se realizó con el objetivo de medir el efecto de tres períodos de destete diferentes (20, 40 y 60 días respectivamente) sobre el Peso de la hembra al destete (PHD), Peso de la camada al destete (PCD) y Peso de la hembra al segundo parto (PHP2) en conejas primíparas. Para el análisis de los datos fue utilizado un Diseño Completamente Aleatorio (D.C.A.) con 4 repeticiones (hembras primíparas) para el destete de 20 días, 5 repeticiones para el destete de 40 días y 4 repeticiones para el destete de 60 días. La información utilizada para los análisis estadísticos provino de datos recaudados en registros reproductivos, de un conejar compuesto de 13 conejas y un padrote. La edad y peso promedio de los animales al inicio del ensayo fueron homogéneos (7 meses y 3.007 Kg respectivamente). El ensayo se realizó en el municipio de Rivas ubicado a 111 km de la ciudad de Managua, a 11º 26' de latitud Norte y 85º 44' de longitud Oeste, a una elevación de 57.77 m.s.n.m. Las variables en estudio fueron: Peso de la hembra al destete (PHD), Peso de la camada al destete (PCD), Peso de la hembra al segundo parto (PHP2). Los valores y desviación estándar para dichas variables fue de : 2.94483 ± 0.3071 Kg, promedios 2.8629 ± 1.5308 Kg y 3.0635 ± 0.2212 Kg, respectivamente. En el ANDEVA realizado para las diferentes variables, el efecto de los tratamientos sobre el Peso de la hembra al destete resultó no significativo. No así, para con las variables Peso de la camada al destete (PCD) y Peso de la hembra al segundo parto (PHP2), donde el efecto de los tratamientos sobre estas fue significativo. El efecto de la covariable (Peso de la hembra al primer parto) solamente resultó significativo para la variable Peso de la hembra al destete (PHD). Mediante la Separación de medias por la Prueba de DUNCAN se obtuvieron los siguientes promedios de las variables por tratamiento; Peso de la hembra al destete (PHD): 1.3469 Kg (t: 20 días), 2.9508 Kg (t: 40 días) y 2.9194 Kg (t: 60 días). Para el Peso de la camada al destete (PCD), los valores fueron: 1.3469 kg (t: 20 días), 2.6571 Kg (t: 40 días) y 4.6363 Kg (t: 60 días). Para el Peso de la hembra al segundo parto (PHP2) los valores fueron: 3.2895 Kg (t: 20 días), 3.0030 Kg (t: 40 días) y 2.9131 Kg (t: 60 días). Con la realización del Análisis de los Costos para hembras, se determinaron valores de 105.29, 127.42 y 148.65 (córdobas), para una hembra al destete en los tratamientos de 20, 40 y 60 días de destete respectivamente. Los costos para una hembra al segundo parto fueron: C$ 130.77 (t: 20 días), C$ 147.03 (t: 40 días) y C$168.26 (t: 60 días). Para gazapo al nacimiento los costos por tratamiento fueron los siguientes: C$ 4.43 (t: 20 días), C$ 4.60 (t: 40 días) y C$ 4.87 (t 60 días. Así también, se determinaron los costos de un gazapo al destete, obteniéndose valores de C$ 7.90, C$ 11.53 y C$15.82 para los tratamientos de 20, 40 y 60 días de destete respectivamente.

微/纳米氧化锌（ZnO）的生长、性质及其应用研究

纳米氧化锌（ZnO）是一种直接宽带隙半导体材料，室温下其禁带隙宽为本3.37 eV，激子束缚能为60 meV。纳米ZnO有明显的尺寸效应、表面和界面效应等，物理化学性能优越。在压电材料、铁电材料、平面显示、表面声波、传感器、场发射器件、激光、光催化等方面有着广泛的用途。近年来，对纳米ZnO材料的研究成为国内外的一个热点。 本论文研究了用化学气相沉积（CVD）法制备微/纳米ZnO材料。通过控制实验条件，合成了多种特殊结构和形貌的微/纳米ZnO材料，并用扫描电子显微镜（SEM）、高分辨率透射电镜（HR-TEM）、X-射线衍射仪（XRD）、Raman光谱和光致发光（PL）等对材料的结构和光学性能进行了表征。采用CVD法，在温度为630 °C，氧气流量为15 sccm，氩气流量为300 sccm的条件下，制备了一种纳米带冠四足状ZnO（T-ZnO）。此结构ZnO材料的每根足顶端均有一规则的六方帽形结构，具有很大的比表面积。实验结果表明：合成的ZnO材料为纤维锌矿结构单晶，并且沿着(0001)方向生长；室温下的PL谱有两个激发峰，一个是在393 nm处相对较弱的近带紫外峰，另一个是在511 nm处强峰。而材料在600 °C下氧气中退火30 min后，511 nm附近的绿光激发辐射峰则基本消失了，这说明在511 nm处的绿光激发辐射峰可能是由于氧空位引起的。此外，通过改变实验条件，还得到了其他多种结构的微/纳米ZnO材料。 通过大量实验，找到了一种在低温下合成微/纳米ZnO材料的新方法，即水蒸气氧化法。用ZnI2作为锌源，水蒸气作为氧化剂，实验温度在300～500 °C范围内，大大低于通常CVD法的500～1500 °C。采用此法，用硅做基底，得到了一系列有趣的实验结果，大多数情况下ZnO纳米晶自组装成很规则的圆。而在瓷舟中收集到的纳米ZnO跟普通CVD法结果相似，可以得到锥状、棒状等结构的纳米晶，但其生长方式与硅基底上的有很大差别。此外，用水蒸气氧化法，还实现了ZnO纳米晶在碳纳米管（CNTs）上的直接生长，而且其PL性能增强，这可能是纳米ZnO和CNTs相互耦合的结果。在700 °C温度下，以锌粉和ZnI2作为锌源，用水蒸气作为氧化剂，在硅基底的正反面分别得到了纳米棒和纳米推子阵列。此外，还对水蒸气氧化法的化学反应机理进行了分析，实验结果证明：固态ZnI2在受热和一定真空度下先蒸发成ZnI2分子，ZnI2分子遇到水蒸气发生反应生成偶极ZnO分子，这些ZnO偶极分子在硅基底上通过静电力自组装成特殊的几何形状。 此外，还通过分子动力学模拟的方法，对材料的力学性能进行了研究，得到了ZnO的弹性常数和体弹性模量，模拟值跟其他研究人员的实验和模拟结果吻合得很好，并估出算了ZnO晶体的表面能和断裂韧性。 本论文还对制备材料的光催化性能进行了系统的研究，采用CVD法制备ZnO，对铬黑T（EBT）进行光催化降解实验。通过正交实验方法，得到了ZnO催化降解EBT的最佳工艺条件，即催化剂用量为5 g/L，光照强度为120 W，反应温度为20 °C，反应时间为120 min，EBT浓度为10 mg/L，溶液pH值为4。 在最佳实验条件下，20分钟内有95%的EBT被降解完，30分钟内则全部降解。因此，ZnO在EBT的降解中催化效率很高，在废水处理中具有潜在的应用前景。

中国西北地区分布的几种荒漠植物的生理生态学特性研究

白沙蒿(Artemisia sphaerocephala Krasch.)是中国西北部沙漠的流动及固定沙丘上广泛分布的优势种灌木。瘦果小而轻;借助显微镜和扫描电镜对瘦果的形态结构进行了观察，其种子的种皮与果皮愈合，果皮外层为很厚的粘液层，其粘液层在遇湿后迅速吸水膨胀，其重量增至原来的589倍。在自然生境中，粘液物质将沙粒粘附于瘦果的周围，使瘦果的重量发生变化。瘦果能长时间在水上漂浮，粘液物质有助于种子的萌发和苗的发育。白沙蒿产生三种不同颜色的瘦果，其种子具有不同的萌发速率但最终达到相同的萌发率。瘦果的粘液物质对白沙蒿种子的传播与萌发具有重要的生态意义。白沙蒿种子为需光种子，种子在光下萌发而在暗中受到抑制。种子萌发的适宜温度为250 C，在100 C和300 C萌发速率和萌发率都很低，萌发在50 C受到抑制。种子在沙中被埋越深，其萌发速率和萌发率就越低。在沙平面下2厘米或更深层沙土下出苗率为零。但是，当将种子上层沙土移走，只保留0.5厘米沙土覆盖种子，这些种子的萌发率达到原先就位于沙土下0.5厘米的种子的萌发率，但是后者的萌发速率较高。土壤水分含量越高，从1. 7%到14. 7%，其萌发就越快。土壤水分含量从19.4%起，种子的萌发受到了延迟，苗的发育受到了抑制。 梭梭(Haloxylon ammodendron)是我国西北荒漠中分布的多年生植物，属中亚荒漠植被成分。其种子萌发的最适温度为loo C，亚适宜温度为15-20 0C。从200C起，温度越高，萌发比率越低。种子无论在光下和暗中都能萌发，萌发率无显著性差异。浓度低于0.2 molL的NaCl溶液对萌发的影响不大;但从0.8 mol/L起，萌发率随着浓度增高而降低，直至为零。将在盐溶液中处理9d的种子转移至蒸馏水后，原来较高浓度下的种子具有较高的萌发恢复率。不同浓度下的种子的萌发率和萌发恢复率要比蒸馏水中的低，表明NaCl处理后的部分种子永久地失去萌发力。梭梭的种子为短命种子，在自然状态下，种子的含水量为8.5%，寿命约为10个月。将梭梭种子含水量降至2. 5%和1.4%，其耐贮藏力增强。经过500 C下5天和10天的人工加速老化后，超干种子表现出较强的抗老化能力。与对照相比，超干种子萌发率、根长及活力指数等均显著提高。较低的电导率和较高的脱氢酶活性，说明种子在超干处理后表现出了膜系统的完整性和较高的种子生活力。超干处理既能显著提高梭梭种子的耐贮性，也能有效保持种质的稳定性，是梭梭种质资源保护的重要途径之一。 沙柳（Salix psammophila）是毛乌素沙地流动沙丘和固定沙丘上广泛分布的重要固沙植物。沙柳叶片的光合速率呈现出双峰型的日动态变化，在午后14点出现光合午休现象。蒸腾速率呈现出单峰型的日动态变化，蒸腾在午后15点达到最大。水分利用效率在早晨9点后保持在2.5 μmol C02．mmol-l H20左右。叶片水分亏缺也表现出规律性的变化。从早晨开始，叶片水分亏缺逐渐增强，在18时达到最大值。比较生长季节的不同时期环境因子的变化情况表明，春末的光照强度和气温比夏末高，但土壤水分含量则相反。沙柳在春末的光合速率、蒸腾速率分别是夏末的79%和72.4%，表明水分亏缺是影响沙柳生长发育的主要限制因素。

毛乌素沙地油蒿与籽蒿种子萌发对光照的反应

油蒿(Artemisia ordosica)与籽蒿(Artemisia sphaerocephala)为毛乌素沙地的优势物种，广泛用于我国北方干旱、半干旱区的生态恢复。油蒿与籽蒿种子萌发对温度、水分等环境条件的反应已有较为明确的研究结果，但关于这两种蒿属植物种子萌发对光照反应的研究目前存在两种不同的结论，对飞播技术的改善造成一定影响。 影响油蒿与籽蒿种子萌发对光照反应的因素较多。如种源地、结实部位、种子颜色、种子保存方式与时间、实验条件、温度等。考虑种源地、种子保存时间与方式、结实部位及温度，从多方面系统研究油蒿与籽蒿种子萌发对光照的反应。结果表明当温度较低时(10:20C)，萌发率和萌发速率在黑暗条件下显著高于在光照条件下。采自榆林地区的种子萌发状况相对较差，萌发率和萌发速率在大多数情况下显著低于其他两地;各种源地上下部种子萌发率有一定差异，大多数结实部位为上部的种子最终萌发率和萌发速率高于下部的种子;保存几周的种子萌发率变化不大，但在温度较高和较低时，随着种子保存时间的延长，萌发率下降较快，而在适宜温度下种子萌发率变化不明显;种子保存方式的不同造成种子萌发情况的差异，但差异不明显;黑暗条件下比近似黑暗条件下的种子萌发率略低。上述因素对种子萌发均具有一定影响，但总体特征是种子萌发对光照的反应表现为强光抑制种子的萌发，黑暗促进种子萌发。当温度较高时(15:25C)，光照与黑暗条件下种子萌发率差异不大，但黑暗条件下种子的萌发速率显著高于光照条件下;当其它条件相同时，种子萌发率和萌发速率显著高于温度较低时(10:20C)。因而，适宜的温度和黑暗条件有利于油蒿与籽蒿种子的萌发。在飞播实践时应为种子创造一定的沙埋条件，创造有利于种子萌发的黑暗环境，促进种子的萌发，提高飞播工作的成效。

海南黄牛和徐闻黄牛线粒体DNA的多态性及其品种分化关系

以14种限制性内切酶分析来自海南岛的海南黄牛和雷州半岛的徐闻黄牛的线粒体DNA限制性片段长度多态性(mtDNA RFLP)。结果只有一种限制性内切酶(sal I)在海南黄牛中检测到多态性, 且其中的C型(15.0, 1.3)尚未见报道。结果还显示, 两个品种6个个体的mtDNA基因单倍型全部表现为A型, 即瘤牛的血统, 并表明两个品种的亲缘关系很近。

Bacillus pallidus sp nov., isolated from forest soil

A Gram-positive bacterium, designated strain CW 7(T), was isolated from forest soil in Anhui Province, south-east China. Cells were strictly aerobic, motile with peritrichous flagella and rod-shaped. The strain grew optimally at 30-37 degrees C and pH 7.0-8.0. The major fatty acids of strain CW 7(T) were anteiso-C-15:0, iso-C-15:0 and anteiso-C-17:0. The predominant menaquinone was MK-7. The cell-wall peptidoglycan contained meso-diaminopimelic acid. The G + C content of the genomic DNA was 42.3 mol%. Phylogenetic analysis indicated that strain CW 7(T) belonged to a monophyletic cluster within the genus Bacillus and showed 16S rRNA gene sequence similarities of less than 96.5% to recognized species of the genus Bacillus. The results of the polyphasic taxonomic study, including phenotypic, chemotaxonomic and phylogenetic analyses, showed that strain CW 7(T) represents a novel species of the genus Bacillus, for which the name Bacillus pallidus sp. nov. is proposed. The type strain is CW 7(T) (=KCTC 13200(T)=CCTCC AB 207188(T)=LMG 24451(T)).