瓜蚜寄主植物对多异瓢虫捕食功能反应的影响

本研究比较了瓜蚜Aphis gossypii Glover 5种主要寄主植物对多异瓢虫Hippodamia variegta(Goeze)捕食功能反应的影响。结果表明,瓜蚜寄主植物对多异瓢虫功能反应有显著的影响。在大多数猎物密度下, 1~3龄幼虫对南瓜和黄瓜上瓜蚜的捕食量较瓢葫芦和哈密瓜上的高;在蚜虫密度较低时（≤ 50头/皿）,4龄幼虫和成虫对南瓜和黄瓜上瓜蚜的捕食量较高,而蚜虫密度≥ 70头/皿时,对瓢葫芦和搅瓜上瓜蚜的捕食量较高。多异瓢虫各龄幼虫和成虫对5种寄主植物上瓜蚜的功能反应均符合Holling II反应。随着瓢虫龄期的增大,猎物处理时间缩短,瞬时攻击率增大,最大捕食量增加。多异瓢虫成虫处理猎物的时间较长于4龄幼虫,而瞬时攻击率和最大捕食量小于4龄幼虫。多异瓢虫捕食不同寄主植物上饲养的瓜蚜时,猎物处理时间、瞬时攻击率和最大捕食量不同。     

七星瓢虫成虫对枸杞木虱的捕食作用

为了测定七星瓢虫成虫对枸杞木虱4种虫态的捕食作用,分别在室内测定七星瓢虫的捕食功能反应、种内干扰、自身密度干扰、捕食偏好性以及在田间七星瓢虫对枸杞木虱的捕食效果.结果表明: 七星瓢虫对枸杞木虱的捕食功能反应符合Holling Ⅱ型方程,其中对卵的最大捕食量为112.6粒,对1～2龄若虫、3～5龄若虫、成虫的最大捕食量分别为536、415和113.9头;田间罩笼试验结果证明,七星瓢虫成虫在其生长周期30 d内能使枸杞木虱总虫口密度下降80.1%;七星瓢虫对1～2龄枸杞木虱若虫的搜寻效率参数a=0.9451,处理时间参数T_h=0.001865,整体优于卵、3～5龄若虫与成虫,且在每皿100头的猎物密度下七星瓢虫的最大捕食率能达80.2%,益害比参考值为1∶100.七星瓢虫对枸杞木虱的捕食作用受自身密度的影响显著大于种内干扰.在混合猎物密度为每皿100头下,七星瓢虫更偏好木虱成虫,在密度为每皿300头下,七星瓢虫更偏向于木虱若虫.表明七星瓢虫是很有控制潜力的捕食性天敌,人工释放七星瓢虫成虫可有效取食枸杞木虱初孵若虫,降低木虱为害.     

中华草蛉、龟纹瓢虫和异色瓢虫对B型烟粉虱的捕食功能反应

室内研究了中华草蛉Chrysopa sinicaTjeder、龟纹瓢虫Propylaea japonica(Thunberg)和异色瓢虫Leis axyridis(Pallas)对B型烟粉虱Bemisiatabaci(Gennadius)若虫的捕食功能反应和寻找效应。结果表明,3种天敌成虫和幼虫的捕食量均随着猎物密度的增加而上升,当猎物增加到一定水平,捕食量趋向稳定,捕食功能反应曲线符合HollingⅡ型方程。异色瓢虫、中华草蛉和龟纹瓢虫成虫和幼虫对烟粉虱若虫的捕食量差异显著,理论最大日捕食量分别为417,263,156头和625,238,108头。3种天敌对烟粉虱若虫的寻找效应随着天敌密度的增加而下降,干扰作用逐渐增强,其寻找效应表现为龟纹瓢虫(0.5656)>异色瓢虫(0.4371)>中华草蛉(0.4029),对烟粉虱的控制能力表现为异色瓢虫>龟纹瓢虫>中华草蛉。     

七星瓢虫成虫对绣线菊蚜捕食作用的室内测试

在实验室内测定了七星瓢虫成虫对苹果绣线菊蚜的捕食作用,结果表明,七星瓢虫成虫对绣线菊蚜密度的功能反应可用Holing-Ⅱ型圆盘方程较好地拟合,捕食作用在一定范围内随猎物密度的增加而加大;七星瓢虫成虫对绣线菊蚜的捕食作用率随着自身密度增加而减小,相互之间存在一定的干扰,自身密度的功能反应能用Hassell数学模型较好地反映。     

多异瓢虫成虫对枸杞木虱的捕食作用

【目的】为了测定多异瓢虫Hippodamia variegata(Goeze)成虫对枸杞木虱Paratrioza sinica Yang&Li的捕食作用。【方法】在室内测定了多异瓢虫的捕食功能反应、种内干扰、自身密度干扰、捕食偏好性,并通过罩笼试验研究多异瓢虫在田间对枸杞木虱的捕食效果。【结果】结果表明,多异瓢虫对枸杞木虱的捕食功能反应符合HollingⅡ型方程,对卵、1~2龄若虫、3~5龄若虫以及成虫的最大捕食量分别为80.4粒、410.0头、350.8头和102.5头。田间罩笼试验结果证明,在多异瓢虫成虫生长周期30 d内能使枸杞木虱总虫口密度下降85.4%;多异瓢虫对枸杞木虱成虫的搜寻效率a=0.8252为4种木虱虫态最佳,而对枸杞木虱卵处理时间Th=0.002283为4种木虱虫态中最佳;在100头/皿的猎物密度下多异瓢虫均能展现其最大捕食率,益害比参考值为1∶100。多异瓢虫对枸杞木虱的捕食作用受自身密度的影响显著大于种内干扰;在100头/皿混合猎物密度下,多异瓢虫更偏好木虱成虫,在300头/皿下,多异瓢虫更偏向于木虱若虫。【结论】研究表明,多异瓢虫是具有控制潜力的捕食性天敌,人工释放多异瓢虫成虫可有效防治枸杞木虱。     

两种瓢虫对刺槐蚜的捕食作用

在实验室条件下研究了龟纹瓢虫成虫和异色瓢虫成虫对不同密度刺槐蚜的捕食功能反应,符合HollingⅡ 型功能反应模型,其模型分别为:Na=0.4050/1+0.0073N和Na=0.4227N/1+0.0046N,x2值均小于X20. 05=9.49,最大捕食量分别为55.6头和90.9头.圆盘方程理论值与实测值相符.随着瓢虫密度的增加,单个瓢虫捕食率下降,龟纹瓢虫和异色瓢虫自身密度的干扰效应模型分别为:E=0.208P-0.235,E=0.236P-0.324.     

不同龄期异色瓢虫对烟蚜的捕食潜能研究

异色瓢虫是烟田烟蚜的优势天敌种类之一,本文在室内进行了异色瓢虫成虫及各龄幼虫对烟草蚜虫的捕食功能反应试验,采用Holling-Ⅱ型功能反应模型进行拟合以明确其捕食潜能,利用Hassell模型和Watt模型拟合并测定了异色瓢虫种内干扰以及自身密度对烟蚜捕食作用的影响,结果表明:异色瓢虫各虫态对烟蚜的捕食量有明显的差异,在相同的烟蚜密度条件下,异色瓢虫4龄幼虫的日最大捕食量最大,为107.41头;其次是成虫,其日最大捕食量为94.34头;3龄幼虫、2龄幼虫和1龄幼虫的日最大捕食量分别为40.32头、14.25头和12.15头。在一定空间和相同比例猎物存在的条件下,种内干扰作用对1龄异色瓢虫幼虫的捕食量影响最为明显,干扰常数为1.1731,而对4龄幼虫干扰最小。各虫态自身密度对其捕食作用的干扰效应明显,1-4龄异色瓢虫幼虫以及成虫的竞争参数b值分别为0.5199、0.1848、0.1351、0.6757、0.6528。本研究表明异色瓢虫对烟蚜捕食潜力很大,尤其是4龄幼虫及成虫对烟蚜具有较大的捕食潜能。     

孪斑唇瓢虫成虫对桑白蚧的捕食功能

在实验室条件下,研究孪斑唇瓢虫Chilocorus geminus Zaslavskij成虫对桑白蚧Pseudau lacaspis pentagona(Targioni-Tozzetti)各虫态的捕食功能反应,寻找效应和干扰效应。结果表明,孪斑唇瓢虫成虫对桑白蚧各虫态的功能反应均符合Holling-Ⅱ型圆盘方程。孪斑唇瓢虫成虫对桑白蚧各虫态的寻找效应随自身密度的增加而降低。根据Holling-Ⅲ型功能反应新模型拟合出1头孪斑唇瓢虫成虫对桑白蚧各虫态的最佳寻找密度分别为:成虫26.7头、卵185.2粒、1龄若虫47.9头、2龄若虫46.8头。当孪斑唇瓢虫成虫与桑白蚧各虫态的数量同比例增加时,孪斑唇瓢虫成虫个体间的相互干扰系数为0.3901,0.7891和0.9827;当桑白蚧2龄若虫数量不变而孪斑唇瓢虫成虫数量增加时,孪斑唇瓢虫成虫个体间的相互干扰系数为0.0960。     

异色瓢虫对白毛蚜捕食作用的研究

试验研究了异色瓢虫Leis axyridis(Pallas)各龄幼虫和戌虫对白毛蚜Chaitophorus po-pulialbae无翅成蚜的捕食功能反应及其成虫的寻找效应。功能反应均属Holling II型。异色瓢虫成虫寻找效应和自身密度之间的关系用Hasell & arley(1969)模型E=QP-m 和Beddington(1975)模型E=aT/［1+btm(P-1)]进行了模拟,Beddington模型更好地反映寻找效应和瓢虫密度之间的 关系。寻找效应与瓢虫成虫自身密度和蚜虫密度之间的关系用Bcddington(1995)模型E＝aT/[1+aT_mN十bt_m(P-1)]进行描述,表明寻找效应(E)随瓢虫密度(P)和猎物蚜虫密度(N)的增大而下降     

六斑月瓢虫对菊小长管蚜的捕食作用

六斑月瓢虫对菊小长管蚜的捕食功能反应符合HollingⅡ型方程。功能反应受到温度、容器大小和捕食者密度的影响。在同一温度下,六斑月瓢虫的捕食量随着猎物密度的增加而增大,寻找效应随着猎物密度的增加而降低。在15℃～25℃范围内,随着温度的升高,捕食的菊小长管蚜高龄若蚜头数增多,而在25℃～35℃有相反的趋势,以25℃下的捕食数量最大,平均达95头/天,捕食上限达392.1头。相同猎物密度条件下,温度与六斑月瓢虫捕食作用的关系可用二次曲线拟合,捕食的最适温度（25℃左右）与菊小长管蚜发生高峰季节的温度相吻合。六斑月瓢虫的捕食作用有较强的种内干扰反应,随着捕食者密度的增大,平均捕食量逐渐减少,捕食作用率也相应地降低,搜索常数Q为0.9003,干扰系数m为0.9816,E=0.9003P^-0.9816。实际应用时,要充分考虑气象因子、瓢蚜密度比等对防效的影响,以期获得最佳防治效果。     

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.     

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.     

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.