广东橘小实蝇寄生蜂调查

本文记述广东省橘小实蝇的寄生蜂4科8种,包括茧蜂科Braconidae的阿费氏茧蜂Fopius arisanus（Sonan,1932）、凡氏费氏茧蜂Fopius vandenboschi（Fullaway,1952）、长尾全裂茧蜂Diachasmimorpha longicaudata（Ashmead,1905）和弗氏短背茧蜂Pasyttalia fletcheri（Silvestri,1916）、姬小峰科Eulophidae的印啮小蜂Aceratoneuromyia indica（Silvestri,1910）、小蜂科Chalcididae的吉氏角头小蜂Dirhinus giffardii（Silvestri,1914）和匙胸瘿蜂科Eucoilidae的柔匙胸瘿蜂属Aganaspis sp．1和Aganaspis sp．2。     

橘小实蝇寄生蜂切割潜蝇茧蜂的人工繁殖技术

切割潜蝇茧蜂[Psyttalia incisi(S ilvestri)]是福建疫区寄生于橘小实蝇[Bactrocera dorsalis(Hendel)]幼虫—蛹期的重要本地寄生蜂。利用室内大量繁殖的橘小实蝇幼虫作为寄主,在室内条件下对其进行人工繁殖技术研究,并设计了人工繁蜂的质量控制和工艺流程。旨在将来提供足够数量的寄生蜂来满足田间放蜂的需要,尽早实现对橘小实蝇的持续、有效地治理。     

应用寄生蜂和不育雄虫防控田间橘小实蝇

食品安全已成为当今社会广受关注的问题。尽管国内的一些学者就阿里山潜蝇茧蜂[Fopius arisanus(Sonan)]和橘小实蝇SIT技术分别开展了不同程度的研究,然而关于应用该蜂和不育雄虫对橘小实蝇[Bactrocera dorsalis(Hendel)]进行田间联合防治的研究还未见相关报道。为此,为探讨天敌昆虫和雄性不育技术对橘小实蝇的田间综合治理(IPM)技术,开展了阿里山潜蝇茧蜂和橘小实蝇不育雄虫的田间释放试验:首先应用性引诱剂降低田间野生雄虫数量;而后,释放橘小实蝇不育雄虫,进一步降低田间橘小实蝇种群数量;最后,释放阿里山潜蝇茧蜂对田间残余的橘小实蝇卵进行追踪寄生,以达到持续控制的目的。通过监测整个防控期田间橘小实蝇的种群数量以及果实受害率和防治效果作为评价指标评价该防治方法的综合防治效果。结果表明:应用阿里山潜蝇茧蜂、橘小实蝇不育雄虫并配合引诱剂的综合措施对橘小实蝇的种群数量有明显控制作用,田间总体防治效果可达90%左右。此外,提出完善橘小实蝇田间防控措施的建议,并提出该研究的不足以及有待进一步开展研究的方向。     

布氏潜蝇茧蜂对橘小实蝇幼虫寄生作用的研究

在试验室条件下研究了布氏潜蝇茧蜂Fopius vandenboschi(Fullaway)的寄生习性。结果表明:该寄生蜂嗜好寄生低龄的橘小实蝇幼虫;橘小实蝇幼虫的密度对布氏潜蝇茧蜂的寄生有明显的影响;被寄生的幼虫数随寄主自身密度的增加而增加,当寄主幼虫密度达每果片30只以上时,寄生数量的增加幅度就趋于下降,用Holling圆盘方程模拟为Na=0.9051N/(1 0.0163N)。此外,布氏潜蝇茧蜂的自身密度对寄生作用也有影响,随着寄生蜂数量的增加,寄生蜂的发现域逐渐变小,用Hassell-Varley方程表示为α=0.4655P-0.5807。     

基于CiteSpace的国内实蝇科寄生蜂研究可视化分析

为了全面客观地了解近国内实蝇科寄生蜂的研究现状和发展脉络,为从事该科昆虫研究和利用的学者与决策者提供数据参考,本文从文献计量学角度,利用可视化分析工具CiteSpace,从发文时间、数量、作者、机构、关键词的共现和聚类、研究演进等角度,分析了国内实蝇科寄生蜂在CNKI数据库中的文献情况。经CiteSpace分析发现,作者群体中陈家骅贡献量最大、中心度最高;研究机构中福建农林大学发文量最多。从关键词共现分析可知实蝇科寄生蜂研究的高频关键词为橘小实蝇、阿里山潜蝇茧蜂、寄生蜂;经关键词聚类发现实蝇科寄生蜂研究可聚类为阿里山潜蝇茧蜂、体型大小、切割潜蝇茧蜂、养殖方法、瓜实蝇5个方向。并通过关键词时间序列的可视化展示,直观地了解国内实蝇科寄生蜂研究的发展脉络。     

长尾潜蝇茧蜂对橘小实蝇幼虫的寄生效能

以橘小实蝇幼虫为寄主,在(25±1)℃,RH(70±10)%,光照周期14L∶10D的条件下,研究了在不同密度的寄生蜂与寄主条件下的长尾潜蝇茧蜂寄生效能。结果表明:不同密度的橘小实蝇幼虫对长尾潜蝇茧蜂的寄生作用有明显的影响,其寄生效应符合功能反应模型HollingⅡ型,方程为Na=0.7291No/(1 0.02362No)。长尾潜蝇茧蜂自身密度对寄生作用也存在干扰效应,用Hassell-Varley模型可表示为a=0.1993P-0.2966。     

湿度对橘小实蝇及寄生蜂存活与发育的影响

研究外来入侵害虫橘小实蝇及其寄生蜂在不同湿度条件下的存活与发育能力,以预测其在福建的适生分布区。结果表明:在25℃条件下,不同相对湿度对切割潜蝇茧蜂成蜂种群寿命影响大小依次为75%>95%>55%>35%,其中75%相对湿度下种群平均寿命最长,采用二次曲线模型并求得最适相对湿度为75.2%;不同相对湿度对橘小实蝇种群寿命的影响大小依次为75%>55%>95%>35%,采用二次曲线模型并求得最适相对湿度为68.7%,二者可能具有相似的分布区域。同时,从存活曲线分布的情况来看,切割潜蝇茧蜂在不同湿度下的存活曲线分布较橘小实蝇更集中,表明橘小实蝇对湿度的变化表现出更强的敏感性。同时,湿度低于35%时,不能交配并繁殖后代;处于较高湿度时,对其后代体形大小没有显著影响。     

阿里山潜蝇茧蜂Fopius arisanus的发育起点温度和有效积温

对橘小实蝇卵寄生蜂阿里山潜蝇茧蜂Fopius arisanus(Sonan)的发育起点温度和有效积温进行了研究。结果表明,阿里山潜蝇茧蜂的卵、幼虫、蛹、雌成虫、雄成虫和世代的发育起点温度分别为9.7、8.8、8.5、8.7、8.7和9.3℃;有效积温分别为25.2.200.2、133.6、344.4、242.8和440.2日度。在19-31℃之间,阿里山潜蝇茧蜂的发育历期随温度的升高而缩短。     

寄生蜂对橘小实蝇控害作用的研究进展

橘小实蝇是一种世界性的检疫害虫,危害多种蔬菜和水果的重要害虫。寄生蜂作为橘小实蝇的重要天敌,对其防治起着重要的作用。本文归纳整理了橘小实蝇寄生蜂主要种类及生物学、生态学特性,并对主要寄生蜂的寄生选择偏好性、寄生能力评价、种群消长影响因素以及其保护利用、人工大量繁育技术研究等进行总结,旨在为更好的开展橘小实蝇寄生蜂的研究及最终实现其大规模应用提供一定的参考。     

阿里山潜蝇茧蜂对橘小实蝇卵的寄生效能

在温度25℃、相对湿度75%、光周期L∶D=12∶12的条件下,研究了阿里山潜蝇茧蜂对橘小实蝇卵的寄生效能。结果表明:橘小实蝇卵的密度变化对阿里山潜蝇茧蜂的寄生作用有很大影响,可用功能反应模型HollingⅡ型模拟,其模拟方程为Na=0.9082N0/(1 0.0046N0);阿里山潜蝇茧蜂成虫的自身密度对寄生作用也有较大影响,可用Hassell-Varley模型模拟,其模拟方程为α=0.2858P-0.3448。     

Physicochemical and biological properties of 6(1),6(3),6(5)-tri-O-alpha-maltosyl-cyclomaltoheptaose (6(1),6(3),6(5)-tri-O-alpha-maltosyl-beta-cyclodextrin)

A unique multibranched cyclomaltooligosaccharide (cyclodextrin, CD) of 6(1),6(3),6(5)-tri-O-alpha-maltosyl-cyclomaltoheptaose [6(1),6(3),6(5)-tri-O-alpha-maltosyl-beta-cyclodextrin, (G(2))(3)-betaCD] was prepared. The physicochemical and biological properties of (G(2))(3)-betaCD were determined together with those of monobranched CDs (6-O-alpha-D-glucopyranosyl-alpha-cyclodextrin (G(1)-alphaCD), 6-O-alpha-D-glucopyranosyl-beta-cyclodextrin (G(1)-betaCD), and 6-O-alpha-maltosyl-beta-cyclodextrin (G(2)-betaCD)). NMR spectra of (G(2))(3)-betaCD were measured using various 2D NMR techniques. The solubility of (G(2))(3)-betaCD in water and MeOH-water solutions was extremely high in comparison with nonbranched betaCD and was about the same as that of the other monobranched betaCDs. The formation of an inclusion complex of (G(2))(3)-betaCD with stereoisomers (estradiol, retinoic acid, quinine, citral, and glycyrrhetinic acid) depends on the cis-trans isomers of guest compounds. The cis isomers of estradiol, retinoic acid, and glycyrrhetinic acid were included more than their trans isomers, while the trans isomers of citral and quinine fit more tightly than their cis isomers. (G(2))(3)-betaCD was the most effective host compound in the cis-trans resolution of glycyrrhetinic acid. Among the branched betaCDs, (G(2))(3)-betaCD exhibited the weakest hemolytic activity in human erythrocytes and showed negligible cytotoxicity in Caco-2 cells up to 200 microM. These results indicate unique characteristics of (G(2))(3)-betaCD in some biological responses of cultured cells.     

Spectral and thermodynamic properties of Ag(I), Au(III), Cd(II), Co(II), Fe(III), Hg(II), Mn(II), Ni(II), Pb(II), U(IV), and Zn(II) binding by methanobactin from Methylosinus trichosporium OB3b

Methanobactin (mb) is a novel chromopeptide that appears to function as the extracellular component of a copper acquisition system in methanotrophic bacteria. To examine this potential physiological role, and to distinguish it from iron binding siderophores, the spectral (UV–visible absorption, circular dichroism, fluorescence, and X-ray photoelectron) and thermodynamic properties of metal binding by mb were examined. In the absence of Cu(II) or Cu(I), mb will bind Ag(I), Au(III), Co(II), Cd(II), Fe(III), Hg(II), Mn(II), Ni(II), Pb(II), U(VI), or Zn(II), but not Ba(II), Ca(II), La(II), Mg(II), and Sr(II). The results suggest metals such as Ag(I), Au(III), Hg(II), Pb(II) and possibly U(VI) are bound by a mechanism similar to Cu, whereas the coordination of Co(II), Cd(II), Fe(III), Mn(II), Ni(II) and Zn(II) by mb differs from Cu(II). Consistent with its role as a copper-binding compound or chalkophore, the binding constants of all the metals examined were less than those observed with Cu(II) and copper displaced other metals except Ag(I) and Au(III) bound to mb. However, the binding of different metals by mb suggests that methanotrophic activity also may play a role in either the solubilization or immobilization of many metals in situ.     

Circular dichroism spectra of DNA quadruplexes [d(G(5)T(5))](4) as formed with G(4) and T(4) tetrads and [d(G(5)T(5)). d(A(5)C(5))]2 as formed with Watson-Crick-like (G-C)(2) and (T-A)(2) tetrads

We utilize electrophoresis and find that a thermally treated equimolar mixture of the oligonucleotide d(G(5)T(5)) and its complementary oligonucleotide d(A(5)C(5)) exhibits either two bands or a single band in one lane, depending on the conditions of the incubation solutions. The thermally treated d(G(5)T(5)) solution loaded in a different lane exhibits a single band of the parallel quadruplex [d(G(5)T(5))](4), which is composed of homocyclic hydrogen-bonded G(4) and T(4) tetrads previously proposed. For the thermally treated equimolar mixture of d(G(5)T(5)) and d(A(5)C(5)), the fast band is assigned to a Watson-Crick d(G(5)T(5)). d(A(5)C(5)) duplex, so that the slow band with the same low mobility as that of [d(G(5)T(5))](4) may be assigned to either [d(G(5)T(5))](4) itself or a [d(G(5)T(5)). d(A(5)C(5))](2) quadruplex. If the latter compound is true, this may be the antiparallel quadruplex composed of the heterocyclic hydrogen-bonded G-C-G-C and T-A-T-A tetrads proposed previously. After removing these three bands for the duplex and two kinds of hypothetical quadruplexes, we electrophoretically elute the corresponding compounds in the same electrophoresis buffer using an electroeluter. The eluted compounds are ascertained to be stable by electrophoresis. The circular dichroism (CD) and UV absorption spectra measured for the three isolated compounds are found to be clearly different. For the electrophoretic elution of the hypothetical [d(G(5)T(5))](4) quadruplex, the result of the molecularity of n = 4 obtained from the CD melting curve analysis provides further support for the formation of the parallel [d(G(5)T(5))](4) quadruplex already proposed. For the thermally treated equimolar mixture of d(G(5)T(5)) and d(C(5)A(5)), the fast band with a molecularity of n = 2 corresponds to the Watson-Crick duplex, d(G(5)T(5)). d(A(5)C(5)). The slow band with a molecularity of n = 4 indicates the antiparallel quadruplex [d(G(5)T(5)). d(A(5)C(5))](2), whose observed CD and UV spectra are different from those of [d(G(5)T(5))](4). By electrophoresis, after reannealing the eluted compound [d(G(5)T(5)). d(A(5)C(5))](2), a distinct photograph showing the band splitting of this quadruplex band into the lower duplex and upper quadruplex bands is not possible; but by a transilluminator, we occasionally observe this band splitting with the naked eye. The linear response polarizability tensor calculations for the thus determined structures of the [d(G(5)T(5))](4) quadruplex, the McGavin-like [d(G(5)T(5)). d(A(5)C(5))](2) quadruplex, and the Watson-Crick d(G(5)T(5)). d(A(5)C(5)) duplex are found to qualitatively predict the observed CD and UV spectra.     

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.     

The frequencies of Gm(1), Gm(2), Gm(4), Gm(12), and Inv(1) in Hessen (Germany)

Summary The serum groups Gm(1) [Gm(a)], Gm(2) [Gm(x)], Gm(4) [Gm(f)]. Gm(12) [Gm(b)] and Inv(1) [Inv(1)] of 2000 sera of healthy blood donors from the land Hesse were examined. The results obtained were compared with those known until now. Three persons, not related to each other, possessed the extremely rare phenotype Gm(-1, 2, 4, 12) [Gm (a-x+b+f+)]. In 0.75% of the cases we found a discordant behaviour of the factors Gm(4) and Gm(12) [Gm(f) and Gm(b)].

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Zusammenfassung 2000 Seren von gesunden Blutspendern aus Hessen wurden bezüglich der Gamma-Globulin-Serumgruppen Gm(1) [Gm(a)], Gm(2) [Gm(x)], Gm(4) [Gm(f)]. Gm(12) [Gm(b)] und Inv(1) [Inv(1)] untersucht. Die gefundenen Resultate wurden mit den bisher bekannten verglichen. Drei miteinander nicht verwandte Personen wiesen den äußerst seltenen Phänotyp Gm(-1, 2, 4, 12) [Gm(a-x+b+f+)] auf. In 0.75% der Fälle fanden wir ein diskordantes Verhalten der Faktoren Gm(4) und Gm(12) [Gm(f) und Gm(b)].

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Director: Prof. Dr. W. Wachsmuth

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Director: Prof. Dr. W. Spielmann

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The nomenclature suggested by WHO at a round-table conference over genes, genotypes and allotypes of immunglobulins is used. The conference took place in Geneva on the 1965 31. 5. to the 5. 6. [5].

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With technical assistance of S. Mohs.