西藏嵩草属（莎草科）的修订

在标本观察和野外调查的基础上,对西藏的嵩草属Kobresia植物进行了分类学修订,共确认了36种和1亚种。更正了6个类群的学名,它们正确的名称是K. esenbeckii,K. fissiglumis,K. gammiei,K. littledalei,K. myosuroides ssp. bistaminata和K. vaginosa。有13个名称,即K. angusta,K. cercostachys var. capillacea,K. clarkeana,K. curticeps var. gyirongensis,K. deasyi,K. glaucifolia,K. hookeri,K. nudicarpa,K. prainii var. elliptica,K. seticulmis,K. stenocarpa,K. stenocarpa var. simplex和K. williamsii处理为异名,其中K. prainii var. elliptica,K. glaucifolia和K. stenocarpa var. simplex为新异名。发现了西藏分布的一个新记录种密穗嵩草K. handel-mazzettii。还收录了最近发表的假钩状嵩草K. pseuduncinoides和阔鳞嵩草K. woodii。此外,重新编制了西藏嵩草属分种和亚种检索表,并较为详细地登记了各类群在西藏的分布地点。     

台南并脊天牛种团的订正研究(鞘翅目,天牛科,沟胫天牛亚科)(英文)

对Breuning(1956)提出的Glenea fainanensis 种团重新进行了研究,并为G.fainanensis,G.inlineata和G.subregularis指定了选模.两个种的地位得到了订正:G.inlineata Pic star.nov.由种下地位G.fainanensis v.inlineata Pic,1943提升为种级阶元,G.subregularis Pic stat.nov.由种下地位G.internedivisa v.subregularis Pic,1943提升为种级阶元.G.tenuivittata Gressitt,1951被确认为G.subregularis Pic的新异名.编制了上述3个种的检索表、给出了成虫整体彩色照片和外生殖器照片.     

中国野青茅属(禾本科)一些种类的修订(Ⅱ)

在标本室研究和野外考察的基础上,对中国野青茅属Deyeuxia的一些种类进行了修订.归并了2个名称,即将Deyeuxia sikangensis Keng并入D. scabrescens (Griseb.) Munro ex Duthie作为异名; 将D. levipes Keng并入D. nivicola Hook. f. 作为异名.确认了D. dispar L. Liou和D. agrostioides L. Liou是两个未合格发表的名称,将前者归并于D. scabrescens,后者归并于D. diffusa Keng.     

安徽大别山粒毛盘菌初探

大别山区森林植物极其丰富多样,区内气候温暖湿润,为粒毛盘菌等腐生真菌生长提供了丰富的基物和适宜的气候条件.对该地区粒毛盘菌等相关类群资源进行了研究,报道了粒毛盘菌属7个分类单元,包括Lachnum ciliare,L. nudipes,L.pudibundum,L.ptgmnaeum,L.subpygmaeum,L.sichuanense和L.virgineum,利用物种描述式表明了种的主要特征,并对其中部分种进行了形态学方面的讨论.     

中国野牡丹科植物补充订正

报道了中国野牡丹科Melastomataceae尖子木属Oxyspora一新记录种——柑叶尖子木O. curtisii King,并绘制了特征线条图。另基于花序和花特征的不同, 将翅茎异形木Allomorphia eupteroton Guillaumin var. teretipetiolata C. Y. Wu ＆ C. Chen由变种提升为种, 归入尖子木属, 即翅茎尖子木Oxyspora teretipetiolata （C. Y. Wu ＆ C. Chen） W. H. Chen ＆ Y. M. Shui, 并补充描述了其花部特征。通过扫描电镜观察了它们的花粉和种子形态, 为分类处理提供了佐证。     

中国玉兰属两新种

描述了中国木兰科玉兰属两新种,奇叶玉兰(Yulania mirifolia D.L.Fu,T B Zhao etZ.X.Chen,sp.nov.)和青皮玉兰(Yulania viridula D.L.Fu,T B Zhao et G.H.Tian,sp.nov.)的形态特征和分布情况,并与近缘种进行了比较。     

野螟亚科一新属和二新种记述(鳞翅目,草螟科)

建立了窗野螟属Torulisquama gen.nov.,记述了2新种,即角窗野螟T. ceratophora sp.nov.和椭圆窗野螟T.ovata sP.nov..文中提供了成虫和外生殖器特征图,编制了窗野螟属分种检索表.模式标本保存在南开大学昆虫标本室.     

中国海鼓虾科角鼓虾属分类研究(甲壳亚门,十足目)

对中国海鼓虾科角鼓虾属系统分类进行了研究.角鼓虾全世界共记录34种,其中中国海记录了9种.本文中记录中国海分布的角鼓虾属Athanas 8种,其中对中国海2新纪录种A.polymorphus Kemp和A.squillophilus Hayashi,进行了描记,并提供了中国角鼓虾种检索表.在中国的材料中:A.japonicus、A.ohsimai、A.polymorphus及A.squillophilus 4种的螯足表现了多态性,A.ohsimai和A.squillophilus的螯足多态性也是首次发现和记载.所有研究测量标本均保存在中国科学院海洋研究所.     

提高人类表现的动态光照明

讨论了基于LED和荧光灯光源以及有无紫外线光谱的动态光照明的分类和应用.介绍了基于荧光灯的动态光照明历史.并讨论了发光二极管技术应用于动态光照明的原因.综述了动态光照影响人体皮质醇,褪黑素,警觉性,体温和情绪的作用机理.并介绍紫外线照射的安全标准.提出了一种理想的动态光照明,此种动态光考虑显色指数,色温,光照度,光谱结构和动态变化.     

不丹和锡金直角步甲属种类(鞘翅目,步甲总科,直角步甲族)

直角步甲属Orthogonius Macleay在不丹和锡金原记录仅1种,即卵直角步甲O.opacus Schmidt-Gobel,本文补充了该种的一些分布记录,并描述了产自不丹和锡金的直角步甲属3新种,即喜直角步甲O.himalayicus sp.nov.、杜氏直角步甲O.dureli sp.nov.和长茎直角步甲O.longiphallus sp.nov.,给出了该地区直角步甲属分种检索表.     

Collagen-like triple helix formation of synthetic (Pro-Pro-Gly)10 analogues: (4(S)-hydroxyprolyl-4(R)-hydroxyprolyl-Gly)10, (4(R)-hydroxyprolyl-4(R)-hydroxyprolyl-Gly)10 and (4(S)-fluoroprolyl-4(R)-fluoroprolyl-Gly)10.

For the rational design of a stable collagen triple helix according to the conventional rule that the pyrrolidine puckerings of Pro, 4-hydroxyproline (Hyp) and 4-fluoroproline (fPro) should be down at the X-position and up at the Y-position in the X-Y-Gly repeated sequence for enhancing the triple helix propensities of collagen model peptides, a series of peptides were prepared in which X- and Y-positions were altogether occupied by Hyp(R), Hyp(S), fPro(R) or fPro(S). Contrary to our presumption that inducing the X-Y residues to adopt a down-up conformation would result in an increase in the thermal stability of peptides, the triple helices of (Hyp(S)-Hyp(R)-Gly)(10) and (fPro(S)-fPro(R)-Gly)(10) were less stable than those of (Pro-Hyp(R)-Gly)(10) and (Pro-fPro(R)-Gly)(10), respectively. As reported by B?chinger's and Zagari's groups, (Hyp(R)-Hyp(R)-Gly)(10) which could have an up-up conformation unfavorable for the triple helix, formed a triple helix that has a high thermal stability close to that of (Pro-Hyp(R)-Gly)(10). These results clearly show that the empirical rule based on the conformational preference of pyrrolidine ring at each of X and Y residues should not be regarded as still valid, at least for predicting the stability of collagen models in which both X and Y residues have electronegative groups at the 4-position.     

Synthesis and luminescence properties of a blue-emitting Sr(3.5) Y(6.5) O(2) (PO(4) )(1.5) (SiO(4) )(4.5) :Eu(2+) phosphor

A novel blue‐emitting Sr_3.5Y_6.5O₂(PO₄)_1.5(SiO₄)_4.5:Eu²⁺ phosphor was synthesized via a solid‐state reaction. Powder X‐ray diffraction (XRD) analysis demonstrated that the Sr_3.5Y_6.5O₂(PO₄)_1.5(SiO₄)_4.5 host had a hexagonal crystal structure in the space group P6₃/m and unit cell parameters a = 9.418 Å, c = 6.900 Å. The as‐prepared phosphor showed a blue emission and all the main emission peaks were located at around 466 nm for different excitation wavelengths of 297, 333 and 391 nm. The temperature dependence of the photoluminescence property was investigated in the range 20–250 °C, and the emission intensity decreased to 71% of the initial value at room temperature on increasing the temperature to 150 °C. According to the classical theory of fluorescent thermal quenching, the activation energy (ΔE) for the thermal quenching luminescence of the as‐prepared Sr_3.45Y_6.5O₂(PO₄)_1.5(SiO₄)_4.5:0.05Eu²⁺ phosphor was determined to be 0.20 eV. Copyright © 2011 John Wiley & Sons, Ltd.     

Role of tfdC(I)D(I)E(I)F(I) and tfdD(II)C(II)E(II)F(II) gene modules in catabolism of 3-chlorobenzoate by Ralstonia eutropha JMP134(pJP4)

The enzymes chlorocatechol-1,2-dioxygenase, chloromuconate cycloisomerase, dienelactone hydrolase, and maleylacetate reductase allow Ralstonia eutropha JMP134(pJP4) to degrade chlorocatechols formed during growth in 2,4-dichlorophenoxyacetate or 3-chlorobenzoate (3-CB). There are two gene modules located in plasmid pJP4, tfdC(I)D(I)E(I)F(I) (module I) and tfdD(II)C(II)E(II)F(II) (module II), putatively encoding these enzymes. To assess the role of both tfd modules in the degradation of chloroaromatics, each module was cloned into the medium-copy-number plasmid vector pBBR1MCS-2 under the control of the tfdR regulatory gene. These constructs were introduced into R. eutropha JMP222 (a JMP134 derivative lacking pJP4) and Pseudomonas putida KT2442, two strains able to transform 3-CB into chlorocatechols. Specific activities in cell extracts of chlorocatechol-1,2-dioxygenase (tfdC), chloromuconate cycloisomerase (tfdD), and dienelactone hydrolase (tfdE) were 2 to 50 times higher for microorganisms containing module I compared to those containing module II. In contrast, a significantly (50-fold) higher activity of maleylacetate reductase (tfdF) was observed in cell extracts of microorganisms containing module II compared to module I. The R. eutropha JMP222 derivative containing tfdR-tfdC(I)D(I)E(I)F(I) grew four times faster in liquid cultures with 3-CB as a sole carbon and energy source than in cultures containing tfdR-tfdD(II)C(II)E(II)F(II). In the case of P. putida KT2442, only the derivative containing module I was able to grow in liquid cultures of 3-CB. These results indicate that efficient degradation of 3-CB by R. eutropha JMP134(pJP4) requires the two tfd modules such that TfdCDE is likely supplied primarily by module I, while TfdF is likely supplied by module II.     

The helix-coil transitions of poly (dA)-poly (dT) and poly (dA-dT)-poly (dA-dT)

Helix–coil transition curves are calculated for poly (dA) poly(dT) and poly (dA-dT) poly (dA-dT) using the integral equation approach of Goel and Montroll.⁵ The transitions are described by the loop entropy model with the exponent of the loop entropy factor, k, remaining an arbitrary constant. The theoretical calculations are compared with experimental transition curves of the two polymers. Results indicate that the stacking energies for these two polymers differ by about 1 kcal/mole of base pairs. Also, a fit between theory and experiment was not possible for k > 1.70.     

Induction of in vitro flowering in Dendrobium Madame Thong-In (Orchidaceae) seedlings is associated with increase in endogenous N(6)-(Delta (2)-isopentenyl)-adenine (iP) and N (6)-(Delta (2)-isopentenyl)-adenosine (iPA) levels

We analysed the endogenous cytokinin levels of Dendrobium Madame Thong-In seedlings grown in vitro during vegetative and flowering-inductive periods. HPLC was used to fractionate the extracts and radioimmunoassay (RIA) was used for assay of zeatin (Z), dihydrozeatin (DZ), N(6)-(Delta(2)-isopentenyl)-adenine (iP) and their derivatives. Coconut water used in experiments was found to contain high level (>136 pmol ml(-1)) of zeatin riboside (ZR). Protocorms and seedlings cultured in medium with coconut water were found to contain 0.5-3.9 pmol g(-1) FW of the cytokinins analysed. Seedlings (1.0-1.5 cm) cultured in flowering-inductive liquid medium containing 6-benzyladenine (BA, 4.4 muM) and coconut water (CW, 15%) contained up to 200 and 133 pmol g(-1) FW of iP and iPA, respectively. These levels were significantly higher than all other cytokinins analysed in seedlings of the same stage and were about 80- to 150-folds higher than seedlings cultured in non-inductive medium. During the transitional (vegetative to reproductive) stage, the endogenous levels of iP (178 pmol g(-1) FW) and iPA (63 pmol g(-1) FW) were also significantly higher than cytokinins in the zeatine (Z) and dihydrozeatin (DZ) families in the same seedlings. Seedlings that grew on inductive medium but remained vegetative contained lower levels of iPA. The importance of the profiles of iP and its derivatives in induction of in vitro flowering of D. Madame Thong-In is discussed.     

Biology of Bactrocera (Zeugodacus) tau (Walker) (Diptera: Tephritidae)

The biology of the fruit fly Bactrocera tau, an important horticultural pest, was studied under laboratory conditions at 25°C and 60–70% relative humidity on Cucurbita maxima. The duration of mating averaged 408.03 ± 235.93 min. After mating, the female fly had a preoviposition period of 11.7 ± 4.49 days. The oviposition rate was 9.9 ± 8.50 eggs and fecundity was 464.6 ± 67.98 eggs/female. Eggs were elliptical, smooth and shiny white, turning darker as hatching approached, and measured 1.30 ± 0.07 mm × 0.24 ± 0.04 mm. The chorion has polygonal microsculpturing and is species-specific with polygonal walls. The egg period lasts for 1.3 ± 0.41 days. The duration of the larval period is 1.2 ± 0.42, 1.7 ± 0.48 and 4.0 ± 0.94 days for first, second and third instars, respectively. Pupation occurs in the sand or soil and pupal periods are 7.0 ± 0.47 days. The life cycle from egg to adult was completed in 14.2 ± 1.69 days; the longevity of mated females and males was 130.33 ± 14.18 and 104.66 ± 31.21 days, respectively. At least two to three generations were observed from June 2008 to June 2009.     

Spectroscopic investigations of Er(3+) :CdO-Bi(2) O(3) -B(2) O(3) glasses

This article reports on the optical properties of Er³⁺ ions doped CdO–Bi₂O₃–B₂O₃ (CdBiB) glasses. The materials were characterized by optical absorption and emission spectra. By using Judd–Ofelt theory, the intensity parameters Ω_λ (λ = 2, 4, 6) and also oscillatory strengths were calculated from the absorption spectra. The results were used to compute the radiative properties of Er³⁺:CdBiB glasses. The concentration quenching and energy transfer from Yb³⁺–Er³⁺ were explained. The stimulated emission cross‐section, full width at half maximum (FWHM) and FWHM × values are also calculated for all the Er³⁺:CdBiB glasses. Copyright © 2011 John Wiley & Sons, Ltd.     

Cationic (tripyrrinato)palladium(II) complexes

The formation of cationic palladium(II)complexes [TrpyPd^II]⁺X⁻ by salt metathesis of the respective trifluoroacetates with different salts of weakly coordinating anions X⁻ was investigated. With non-hydrolizable counterions, cationic mono- and dinuclear complexes are observed depending on the nature of the anion X⁻ and the solvent. The mononuclear cations, which are only formed with X = BAr^F, most probably carry a weakly bound molecule of dichloromethane at the fourth coordination site of Pd^II. When treated with diazoalkanes, only these are sufficiently reactive to form carbene complexes. Four- and five coordinate Lewis base adducts [TrpyPd^IIL]⁺ with L = CH₃NC, tBuNH₂, PMe₃, PEt₃ and PiPr₃ and [TrpyPd^IIL₂]⁺ with L = PMe₃ were prepared from the mononuclear cations [TrpyPd^II]⁺BAr^F−. From structural studies it becomes apparent, that the formation of stable five coordinate Pd^II species is restricted to medium size ligands and depends on the delicate balance between the steric influence of L and the strain, which is induced on the TrpyPd^II unit.