昆虫聚集信息素

昆虫聚集信息素是昆虫重要的信息化学物质之一,对昆虫的聚集行为有重要意义。近三十年来,国外鉴定了多种昆虫聚集信息素,主要成分为一些烃、醇、醛、酮、酯、酸、酸酐、胺以及腈类化合物,但其在有害生物可持续治理中的应用潜能尚未充分利用;昆虫聚集信息素的来源多样,除蛹外,多个虫态均有聚集信息素释放,有些学者甚至把一些寄主释放的挥发物作为聚集信息素的组分;同种昆虫,不同生理状态,其聚集信息素可以完全不同或同一信息化学物质的功能不同;但是,并非所有昆虫的聚集行为均为聚集信息素调节,利他素、性信息素以及报警信息素等其它信息化学物质均能导致一些昆虫的聚集。本文综述了5目17科55种昆虫的聚集信息素。     

昆虫利它素

<正> 近年来,在化学生态领域中,对生物间相互关系的形成进行了广泛的研究,现已弄清某些化学物质在这种关系中起着重要的作用。昆虫与昆虫;昆虫与植物之间的联系很大程度上也是依赖化学物质传递信息,例如昆虫求偶、寻找食物、定向栖息场所,搜索寄主、受到侵扰时向同伴告警等过程中都存在化学物质的作用,这类化学物质称为“信号化合物(Semiochemical)”。根据它们的作用过程不同,信号化合物分为两类:一类是种内信号化合物,或者叫做信息素(Pheromone),它是由一种昆虫分泌并释放到体外引起同种昆虫的其它个体产生行为反应的化学物质,当前研究得较为广泛的昆虫性信息素就是属于这一类化合物。另一类是种间信号化合物,或者叫做交互化合物(Allelochemics),它是由一种昆虫分泌并释放到体外引起异种昆虫个体产生行为反应的化学物质。     

信息化合物对昆虫行为的影响

本文综述了来自寄主植物的挥发性物质和同种昆虫或异种昆虫释放的各种信息素及两者的协同作用的信息化合物对昆虫行为的影响。特别强调了寄主植物的气味物质和昆虫信息素协同作用在昆虫寻找寄主、求偶、交配及天敌在寄主识别过程中的重要地位。昆虫对寄主植物的识别是由于识别了植物气味的由一定组分、按照严格比例组成的化学指纹图。昆虫信息素与植物挥发性物质相结合为昆虫寻找求偶、交配场所提供更复杂或更全面的信息。许多昆虫只有在寄主植物或寄主植物气味存在时 ,才能释放性或聚集信息素。天敌在寄主识别、搜索及定位等一系列过程中 ,来自寄主的食料、寄主本身及两者的互作的信息化合物起重要的作用。研究信息化合物对昆虫行为的影响可以探索昆虫各种行为的内在机理 ,更好的了解寄主—昆虫—天敌三层营养关系的相互作用 ,对利用天然活性化合物防治害虫及生物防治提供理论依据     

植物挥发性信息化学物质在昆虫寄主选择行为中的作用

植物信息化学物质在植食性昆虫的寄主定向、产卵、聚集、传粉等行为中发挥着重要作用,对其进行深入研究,不仅有助于阐明植食性昆虫的寄主选择机理,也可为提出新的害虫防治策略提供理论依据.本文概述了近年来昆虫寄主选择定向中起关键作用的植物挥发性信息化学物质的种类、基本特性和作用方式,并就植物挥发性信息化合物应用前景和目前存在的主要问题进行了讨论.     

生物的化学通讯

生物个体（同种或异种）相互之间的有着化学信息联系,昆虫,特别是社会性昆虫化学通讯是其沟通信息的主要方式,我们关于化学通讯的知识大多来自于对昆虫信息素的研究,近来的研究已揭示在植物和植物以及植物和动物之间也存在着化学信息交流。     

寄生蜂取食寄主特性及其在害虫生物防治中的作用

许多寄生性天敌昆虫的雌虫不仅寄生寄主, 而且还能取食寄主。在卵育型（synovigenic）寄生蜂类群中, 取食寄主行为是较为普遍的现象。本文综合近20年相关研究进展, 从寄生蜂类群、取食类型、生态学意义及影响因子等方面对寄生蜂的取食寄主行为进行了归纳总结。寄生蜂通过取食不仅可以杀死寄主, 直接起到控制害虫种群数量的作用, 还能通过取食策略为卵的成熟和再生提供营养来源, 对延长雌虫的寿命也有一定的帮助。对取食寄主行为的了解可为筛选优势寄生性天敌种类、评估寄生蜂在害虫生物防治中的作用提供重要信息。     

同种或异种干扰对花鼠分散贮藏点选择的影响

同种和异种干扰竞争可以增强花鼠(Tamias sibiricus)分散贮食强度,但对其贮藏点选择的影响还不清楚.在半自然围栏内,研究了同种(干扰源为不同性别花鼠)或异种(干扰源为大林姬鼠,Apodemus peninsulae)干扰竞争对花鼠贮藏点选择的影响.结果发现:(1)同种和异种干扰竞争均显著降低了花鼠在高竞争区内的贮藏比例;(2)同种个体存在时,雌性花鼠显著降低了在高竞争区内的贮藏比例,雄性花鼠则显著增加了在中竞争区的埋藏比例.结果表明,花鼠贮藏食物时会避开高竞争区域以降低同种或异种的盗食损失,同时雌雄个体对同种竞争干扰的响应有所差异.     

桑天牛卵长尾啮小蜂的寄主选择定位行为

本文对桑天牛卵长尾啮小蜂Aprostocetus prolixus LaSalle et Huang的寄主选择定位行为进行了系统研究。已有研究表明,寄主植物-寄主昆虫复合体释放的挥发物对寄生蜂有显著的引诱作用。为了查明寄主植物 寄主昆虫复合体中挥发性引诱物质的来源,对不同处理桑枝（正常桑枝、机械损伤桑枝、系统枝、桑天牛Apriona germari（Hope）咬食和产卵桑枝）、桑天牛虫粪及雌雄两性桑天牛所释放的挥发物分别进行了测定。结果显示：不同处理桑枝对寄生蜂都具有显著的引诱作用,而且产卵桑枝的引诱活性最大;桑天牛虫粪的气味对寄生蜂有引诱活性,而雌、雄桑天牛体表挥发物对寄生蜂的引诱效果不明显。桑天牛爬行痕迹对寄生蜂的微栖境接受行为没有影响,而桑天牛虫粪中的信息物质在寄生蜂的微栖境接受过程中起着重要作用。寄生蜂对产卵桑枝段的选择几率明显高于正常桑枝段和咬食桑枝段,而对不同植物上产卵刻槽的选择没有差异; 刻槽表面存在着与此卵寄生蜂寄主识别相关的信息物质。     

昆虫雄性生殖腺分泌物的功能

昆虫两性成功交配后,雄性生殖腺分泌物使雌性昆虫的生理和行为都发生了巨大的改变。昆虫雄性生殖腺分泌物含有多种具有生物活性的分子,这些生物活性分子通过成功交配转移到雌虫生殖道后,对雌虫的生殖活动产生影响,使交配雌虫一段时间内不再交配,使已转移的精子易于在雌虫生殖道内储藏,使卵与精子完成受精过程,还可刺激雌虫产卵和卵的发育,调控排卵和产卵等生殖过程。在精子的转移过程中,雄性生殖腺分泌物中的抗菌媒介质能使雌虫的生殖导管提供友好的环境。此外,一些昆虫的雄性生殖腺分泌物还含有一些有毒的化学物质,保护已产下的卵不被天敌取食和病原体侵染。     

植食性同翅目昆虫寻找和接受植物韧皮部过程中的细胞与化学探试(英文)

植食性同翅目昆虫在最终接受其宿主植物的过程中,将感受从叶表层直到韧皮部筛管途中存在的多种化学物质,并导致不同的刺探和取食行为。本文就植物叶表层存在的糖类和生物碱类物质,叶肉层的多糖类、酸碱度和酚类物质以及韧皮部内的氨基酸、蛋白质、碳水化合物和植物次生物质等对昆虫寻找及取食韧皮部行为的影响作一综述,并且还探讨了植物叶肉层的细胞结构对昆虫刺探及取食行为的可能影响。此外,结合刺探电位(electrical penetration graphs,EPGs)的研究结果,还讨论了昆虫感受植物叶组织内部的各种化学和细胞结构信息的可能机制。     

Scurvy in capybaras bred in captivity in Argentine

In order to determine if the absence of vitamin C in the diet of capybaras (Hydrochoerus hydrochaeris) causes scurvy, a group of seven young individuals were fed food pellets without ascorbic acid, while another group of eight individuals received the same food with 1 g of ascorbic acid per animal per day. Animals in the first group developed signs of scurvy-like gingivitis, breaking of the incisors and death of one animal. Clinical signs appeared between 25 and 104 days from the beginning of the trial in all individuals. Growth rates of individuals deprived of vitamin C was considerably less than those observed in the control group. Deficiency of ascorbic acid had a severe effect on reproduction of another population of captive capybaras. We found that the decrease in ascorbic acid content in the diet affected pregnancy, especially during the first stages. The results obtained suggest that it is necessary to supply a suitable quantity of vitamin C in the diet of this species in captivity.     

Changes in lactate dehydrogenase activity in chicken tissues in hyperthyreosis in ontogenesis

The lactate dehydrogenase activity in reactions of lactate oxidation and synthesis was studied in subfractions of the chicken brain, heart and liver at the embryonal, early postembryonal and adult stages of development after thyroxine administration. It has been shown that during embryogenesis thyroxine predominantly enhanced the rate of lactate oxidation in the mitochondrial tissues. A marked increase in the lactate synthesis was found in cytoplasm of the adult chicken tissues. Specificity of enzyme activity alterations was detected in the chicken brain during ontogenesis after thyroxine administration.     

Role for dopamine in malonate-induced damage in vivo in striatum and in vitro in mesencephalic cultures

Defects in mitochondrial energy metabolism have been implicated in the pathology of several neurodegenerative disorders. In addition, the reactive metabolites generated from the metabolism and oxidation of the neurotransmitter dopamine (DA) are thought to contribute to the damage to neurons of the basal ganglia. We have previously demonstrated that infusions of the metabolic inhibitor malonate into the striata of mice or rats produce degeneration of DA nerve terminals. In the present studies, we demonstrate that an intrastriatal infusion of malonate induces a substantial increase in DA efflux in awake, behaving mice as measured by in vivo microdialysis. Furthermore, pretreatment of mice with tetrabenazine (TBZ) or the TBZ analogue Ro 4-1284 (Ro-4), compounds that reversibly inhibit the vesicular storage of DA, attenuates the malonate-induced DA efflux as well as the damage to DA nerve terminals. Consistent with these findings, the damage to both DA and GABA neurons in mesencephalic cultures by malonate exposure was attenuated by pretreatment with TBZ or Ro-4. Treatment with these compounds did not affect the formation of free radicals or the inhibition of oxidative phosphorylation resulting from malonate exposure alone. Our data suggest that DA plays an important role in the neurotoxicity produced by malonate. These findings provide direct evidence that inhibition of succinate dehydrogenase causes an increase in extracellular DA levels and indicate that bioenergetic defects may contribute to the pathogenesis of chronic neurodegenerative diseases through a mechanism involving DA.     

我国葫芦科植物离体培养研究进展

葫芦科植物包括多种瓜类蔬菜,对其进行离体培养研究具有重要的理论和实践意义。综述了国内在葫芦科植物器官培养、体细胞胚胎发生、花药培养、原生质体培养和体细胞杂交及离体遗传转化等方面取得的研究进展,并对葫芦科植物离体培养、遗传转化与育种的前景作了展望。     

SSTR5 ablation in islet results in alterations in glucose homeostasis in mice

Somatostatin (SST) peptide is a potent inhibitor of insulin secretion and its effect is mediated via somatostatin receptor 5 (SSTR5) in the endocrine pancreas. To investigate the consequences of gene ablation of SSTR5 in the mouse pancreas, we have generated a mouse model in which the SSTR5 gene was specifically knocked down in the pancreatic beta cells (betaSSTR5Kd) using the Cre-lox system. Immunohistochemistry analysis showed that SSTR5 gene expression was absent in beta cells at three months of age. At the time of gene ablation, betaSSTR5Kd mice demonstrated glucose intolerance with lack of insulin response and significantly reduced serum insulin levels. Insulin tolerance test demonstrated a significant increase of insulin clearance in vivo at the same age. In vitro studies demonstrated an absence of response to SST-28 stimulation in the betaSSTR5Kd mouse islet, which was associated with a significantly reduced SST expression level in betaSSTR5Kd mice pancreata. In addition, betaSSTR5Kd mice had significantly reduced serum glucose levels and increased serum insulin levels at 12 months of age. Glucose tolerance test at an older age also indicated a persistently higher insulin level in betaSSTR5Kd mice. Further studies of betaSSTR5Kd mice had revealed elevated serum C-peptide levels at both 3 and 12 months of age, suggesting that these mice are capable of producing and releasing insulin to the periphery. These results support the hypothesis that SSTR5 plays a pivotal role in the regulation of insulin secretion in the mouse pancreas.