穴蚁蛉的自然种群动态

本文主要报道了穴蚁蛉 Myrmeleon(Morter) sagax(Walker)幼虫的野外自然种群数量动态。穴蚁蛉 1年发生 1代 ,在自然界其幼虫 3～ 5月份数量平稳略有下降 ,5、6月间数量迅速下降 ,6月初数量最少 ;7～ 9月份数量迅速上升 ,而后下降 ;新一代穴蚁蛉幼虫 (蚁狮 )在 6月份出现。其种群 ,秋季以 1龄幼虫数量为多 ,冬季主要以 2龄幼虫为主越冬 ,春季以 3龄蚁狮占优势。春季野外采集来的蚁狮 ,在每日光照 14小时、每周两饲 (每次饲 1头米蛾 Corcyra cephalonica成虫 )的条件下饲养 ,结果发现 ,采集回时处于 3龄期的蚁狮比自然界大约提前 1个月结茧化蛹和羽化 ;而采集回时处于 2龄期的蚁狮则和自然界中的情况基本一致。     

粤北蚁狮生态学的初步研究

根据多年来对粤北蚁狮的调查和试验,研究了粤北自然界穴蚁蛉的生活史,蚁狮４种生境类型,５目数十种昆虫食物分布和坐等式的捕食方式．结果表明,在一定范围内,饲食量一定时,饲食频率增大１倍,蚁狮个体发育历期缩短２０％,３５天内幼虫结茧化蛹率提高４１．７５％．     

蚁蛉生物学研究进展

蚁蛉科Myrmeleontidae昆虫的幼虫俗称蚁狮,我国古人很早就将其入药,是一种具有良好开发利用前景的药用昆虫。文章对蚁蛉分类学、生物学、人工饲养、药用价值和杀虫活性物质分离等方面的研究进行综述,以期较全面了解蚁蛉的研究进展,为进一步研究、开发和利用蚁蛉提供参考。     

四种昆虫饵料对穴蚁蛉幼虫生长发育及消化利用的影响

选择4种可规模化饲养的昆虫——米蛾Corcyra cephalonica、家蝇Musca domestica、斜纹夜蛾Spodoptera litura、甜菜夜蛾Spodoptera exigu幼虫来饲养穴蚁蛉Myrmeleon sagax(Walker)幼虫(俗称蚁狮),研究这4种饵料对蚁狮生长发育及消化利用的影响。结果显示,用家蝇幼虫饲养的蚁狮,其体重增长、相对生长率、化蛹率、蛹重均显著高于用斜纹夜蛾和甜菜夜蛾幼虫饲养的蚁狮,而幼虫历期则比斜纹夜蛾和甜菜夜蛾幼虫饲养的短;用米蛾幼虫饲养,虽然蚁狮体重增长、化蛹率和蛹重与用家蝇幼虫饲养的差异不显著,但其相对生长率却显著低于用家蝇幼虫饲养的蚁狮,幼虫历期也比用家蝇幼虫饲养的明显延长。同时食物消化利用的结果显示,用4种饵料饲养蚁狮,它们的近似消化率差异不显著,但食物利用率和食物转化率均以家蝇幼虫饲养的蚁狮最高。经分析比较,在4种饵料昆虫中,以用家蝇幼虫每4d喂蚁狮1次的饲养效果最佳。     

泛蚁蛉对筑穴材料选择性研究

研究了泛蚁蛉幼虫对筑穴材料选择性,并分析了筑穴材料中的含水量对泛蚁蛉幼虫筑穴率的影响.泛蚁蛉各龄期幼虫均偏爱在细上粒中筑穴;各龄幼虫在70～40目颗粒中有最高的筑穴率和最大的穴直径,2、3龄在颗粒组合1/3Ⅰ+1/3Ⅱ+1/3Ⅴ中也有较高的筑穴率和大的穴直径,且筑穴率和穴直径与在70～40目颗粒中无明显差异;当筑穴材料中的含水量小于3%时,各龄泛蚁蛉幼虫均有较高的筑穴率.     

蚁狮的行动

蚁狮是脉翅目(Neruopera)蚁蛉科(Myrmel-eontidae)的幼虫。蚁狮有会做陷阱及不会做陷阱的两种。笔者所叙述的是属于前一种。     

穴蚁蛉幼虫全长均一化cDNA文库的构建

通过构建穴蚁蛉幼虫(俗称蚁狮)全长均一化cDNA文库,以期了解蚁狮的抗菌肽、毒素蛋白以及其它药用蛋白种类,为日后筛选、克隆表达和分离纯化这些药用蛋白奠定基础.用针刺诱导蚁狮产生抗茵物质后,分离纯化总RNA,结合SMART全长文库与DSN(duplex-specific nuclease)均一化技术,构建全长均一化cDNA文库,并通过平板计数和菌落PCR方法鉴定文库.随机挑选192个单克隆进行5′端测序,并与NCBI数据库进行比对分析.结果显示,构建出的文库平均插入片段长度为1 200bp,原始文库的滴度达到7.5×105 CFU/mL,而扩增文库则为1.95×1011CFU/mL.在所挑选的单克隆中,共获得190条有效序列,平均读长1 340 bp,文库重组率达到98.96%.与NCBI数据库比对后发现,这些序列可能是一些编码蚁狮免疫、消化及毒性蛋白的基因.     

真牛假牛分分清

正提到"牛",相信大家的脑海里很快会蹦出许多关键词。动物中有不少叫牛不是牛的动物。它们究竟哪里"牛"呢?咱们看过就知道——沙牛沙牛也叫地牯牛,它们还有个更国际化的名字——蚁狮。蚁狮长得像一种灰扑扑的甲虫。事实上,它们是蚁蛉的幼虫,最喜欢吃蚂蚁、萤火虫等昆虫。蚁狮的头部有两个镰刀状大腭,大多呈张开状,看起来和牛的犄角有几分相似,所以它们被称为沙牛。     

中国棘蚁蛉族分类研究(脉翅目,蚁蛉科)

对中国棘蚁蛉族Acanthaclisini进行了分类研究和修订,共记述中国棘蚁蛉族4属5种(包括2新纪录属、2新纪录种):尾棘蚁蛉Acanthaclisis pallida Mclachlan,单中大蚁蛉Centroclisis negligens(Navás),南击大蚁蛉Heoclisis kawaii(Nakahara),追击大蚁蛉Heoclisis japonica(Maclachlan)和黎母硕蚁蛉Stiphroneura inclusa(Walker).其中棘蚁蛉属Acanthaclisis和硕蚁蛉属Stiphroneura为中国新纪录属,尾棘蚁蛉A.pallida Mclachlan和黎母硕蚁蛉S.inclusa(Walker)为中国新纪录种.确定了Alloclisis hainanica Yang为Centro-clisis negligens(Navás)的新异名,Neriga limoiana Yang为Stiphroneura inclusa(Walker)的新异名.编写了中国棘蚁蛉族分种检索表.标本保存在中国农业大学昆虫系标本馆和中国科学院动物所.     

穴蚁蛉幼虫期的食物量对各虫态历期的影响研究

穴蚁蛉在自然条件下１年发生１代,本实验证明,不同的饲食频率可影响幼虫的发育历期,在每天饲给１头米蛾成虫的情况下,１年可发生３代。１个世代可以在全历期都处于长日照和没有低温的条件下完成,其发育可以不需要光周期变化诱发,１５日饲食１次的穴蚁蛉,３龄 虫     

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.     

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.     

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.