性信息素2，6-二氯酚在长角血蜱交配行为中的作用

长角血蜱Haemaphysalis longicornis的交配行为包括7个时期,行为的完成依赖于性信息素的调节。生物测定表明：雄蜱的行为反应受雌蜱分泌的性信息素影响。堵塞雌蜱盾窝其行为受到抑制,点滴2,6-DCP或雌蜱盾窝腺提取物则被恢复。用气相色谱法测定了雌蜱盾窝腺中2,6-DCP的含量;吸血后1～２天含量最高(11.12 ng/只);吸血后3～５天即交配前下降交维持在一较恒定的水平;吸血后6～７天即交配后明显降低;饱血后检测不到2,6-DCP。2,6-DCP是长角血蜱性信息素的一种成分。     

硬蜱盾窝与盾窝腺的细微结构

用扫描及透射电镜研究硬蜱盾窝与盾窝腺的结构.幼蜱只有横缝状盾窝原基,盾窝腺尚未发育;若蜱盾窝增大,其孔数相应增加;到成蜱阶段,不仅盾窝增大,而且盾窝腺完成发育.对9种雌蜱盾窝进行比较,在其大小和孔数方面有一定差别.亚洲璃眼蜱雄蜱盾窝腺不发达,几个叶瓣贴在一起,组成1—2个腺体组.雌蜱吸血前,叶瓣相互贴在一起.吸血后,球状叶瓣散开,连接叶瓣的导管清楚可见,分泌细胞中颗粒增多,这与其分泌性信息素有关.     

长角血蜱不同发育期盾窝超微结构的比较研究

为阐明蜱类盾窝及其发育特点,用扫描电镜观察了长角血蜱Haemaphysalis longicornis不同发育期盾窝的结构,并分析了血餐对盾窝发育的影响.结果表明：幼蜱仅具1对盾窝原基,且每个盾窝原基有1个盾窝孔;若蜱盾窝有了一定的发育,面积（长径×短径）增大且盾窝孔数增多（2~6个）;成蜱盾窝面积最大,且盾窝孔数达21~35个.盾窝的发育主要在幼蜱蜕皮阶段及若蜱的吸血和蜕皮阶段,雌蜱盾窝孔径显著大于雄蜱（P<0.01）,成蜱、若蜱和幼蜱的盾窝孔孔径在吸血过程中（交配雌蜱除外）各虫期均无显著变化 （P>0.05）.综合分析成蜱与未成熟蜱盾窝孔径,发现它们之间无显著差异 （P>0.05）,这在一定程度上说明蜱类的盾窝孔径在未成熟期可能已经有了雌雄分化.     

蜱类的信息素

<正> 信息素的研究近年有很大进展,昆虫的信息素现在可以分离,提纯,有些还可以合成并在生产实践中应用。近年的研究工作也表明,蜱螨类和昆虫一样,也产生信息素,尤其在蜱类更为普遍。 蜱类的信息素也有两类,即性信息素(sex pheromonc)和集聚信息素(assembly pheromone)。 性信息素在蜱类中普遍存在,现已发现革蜱,花婢、扇头蜱、硬蜱和牛蜱等属的种类都能产生。雌虫在吸血时释放性信息素,以吸引吸食中的雄虫,硬蜱科的性信息素,可用己烷、戊烷或石油醚等有机溶沼提取,它的成分在多数蜱类为2,6-2氯酚(2,6—dichlorophenol),如在血红扇头蜱Rhipicephalus sanguineus(Latreille).安氏革蜱Dermacentor andersoni Stiles,变异革蜱D.variabilis Say等。有些蜱类雌虫的提取物也含有石碳酸     

金泽革蜱的生物学特性研究

金泽革蜱是分布于东洋区的三寄主蜱, 成虫活跃于夏季到晚秋, 其发育历期随季节而不同.雌虫在兔休上吸血时间, 七、八月为16—20天, 十一月只需9天.产卵前期在夏季饱食的雌虫为13—27天;十一月饱食者产生滞育, 至少需244天.产卵期持续31—43天(七、八月), 总产卵量为1749—8995粒.雌虫产卵显与饱血雌虫体重之间有非常显著的正相关(r=0.989, p<0.001).金泽革蜱的产卵力(饱食后每毫克体重产卵数)为7.631.卵期为55—79天(九、十月), 幼虫在兔体上吸血4—6天, 饱食后经18—29天脱皮为若虫, 若虫寿命可达124天.     

雌星豹蛛性信息素的行为学证据

采用星豹蛛(Pardosa astrigera)成熟雄蛛求偶时潜伏时间、静止时间、身体震动和第一墩步足伸展次数等行为参数,利用行为学方法测定了不同性别、日龄和生殖状态的星豹蛛雌蛛释放的拖丝对雄蛛求偶行为的影响。结果表明,雄蛛第一对步足伸展和身体震动等典型求偶行为是进行星豹蛛性信息素生物测定的可靠评价指标。星豹蛛雄蛛能通过拖丝上的性信息素辨别星豹蛛的性别、日龄和生殖状态。雄蛛在成熟3周未交配雌蛛拖丝处理过滤纸上潜伏时间和静止时间都相应最短,在交配未产卵雌蛛、雌亚成蛛和成熟雄蛛拖丝上时间中等,在卵孵化雌蛛拖丝处理滤纸上潜伏时间和静止时间都相应最长。成熟3周未交配雌蛛和交配未产卵雌蛛释放的拖丝都能引起雄蛛第一对步足伸展和身体震动等典型求偶行为,雄蛛对成熟3周未交配雌蛛拖丝典型求偶行为的频率都相应高于交配未产卵雌蛛。卵孵化雌蛛释放的拖丝虽也能引起雄蛛第一对步足伸展行为,但其伸展频率显著降低;而其它拖丝都不能引起雄蛛典型求偶行为。     

实验室条件下长角血蜱的生物学特性研究

实验室条件[(27±1)℃;75%RH;6L：18D]下,长角血蜱完成其生活史需135.8d：卵的孵化期为38.5d：幼虫吸血前期、吸血期和蜕皮前期分别为5.3d,3.8d和13.9d;若虫吸血前期、吸血期和蜕皮前期分别为7.2d,5.4d和16.9d;成虫吸血前期、吸血期、产卵前期和产卵期分别为7.6d,9.4d,7.8d和20.0d。雌虫饱食体重与产卵量之间存在非常显著的正相关(r＝0.9496,P<0.001)。雌虫的生殖效率指数REI＝11.06,生殖适合度指 数RFI＝7.19。生活周期在不同季节无明显变化。雄虫吸血期受雌虫吸引而成功地交配,这一过程是在吸引性信息素的作用下完成的。     

烟夜蛾雄蛾性附腺因子对雌蛾性信 息素合成的抑制作用

烟夜蛾Helicoverpa assulta处女蛾在交配后1 h,其性信息素滴度即显著降低,72 h内未见恢复。生测结果表明,烟夜蛾性信息素合成抑制因子主要来源于雄蛾性附腺。不同日龄雄蛾性附腺提取物的抑制活性无显著差异。光暗期对其活性具显著影响,暗期中雄蛾的性附腺物质对雌蛾性信息素合成具有较强抑制作用,而光期中雄蛾的性附腺物质不具抑制活性。在暗期的不同时间处理,对处女蛾性信息素合成的抑制作用无显著差异。雄蛾性附腺提取物对雌蛾性信息素合成的抑制作用与注射剂量有明显的相关性,0.2 ME（雄蛾当量）是产生显著抑制作用的最小剂量。对交配雌蛾注射性信息素生物合成激活神经肽（PBAN）提取物后,其性信息素合成又可恢复,这说明雌蛾交配后,性信息素滴度降低的原因是由于缺少了PBAN的调控。     

小菜蛾对合成植物挥发物的活性反应

在室内检验了小菜蛾已交配和未交配雌、雄成虫对3种合成植物挥发物乙酸顺-3-己烯酯（Z-3-hexenyl acetate,ACTE）、异硫氰酸丙烯酯（allyl isothiocyanate,NCS）和顺-3-己烯醇（Z-3-hexen-1-ol,OH）的触角电位(EAG)反应。不同浓度（0.008 μg/μL、0.08 μg/μL、0.2 μg/μL、0.8 μg/μL、8 μg/μL、20 μg/μL和40 μg/μL）实验表明,随着刺激化合物浓度的提高,小菜蛾反应活性增强。但小菜蛾的性别及其交配状态可能影响其对3种化合物的反应强度：不同性别及交配状态的小菜蛾对ACTE的反应差异不大;未交配雌、雄虫对OH的反应强于已交配雌、雄虫;未交配雌虫对低浓度的NCS反应较强,NCS超过一定浓度时已交配雌虫的反应强于未交配雌虫,雄虫对NCS反应较小且与交配状态无关。以小菜蛾性信息素作为对照,在湖北长阳和越南河内试验了这3种植物挥发物诱芯（6 μL/诱芯）对小菜蛾的引诱作用。结果表明,在湖北,第1天时 ACTE、NCS对雄虫具有很强的引诱作用,引诱量显著大于性诱剂的引诱量,但随着诱芯放置时间延长,NCS引诱作用迅速下降,第2天时引诱作用已经很小;ACTE的引诱作用下降缓慢,第4天的诱蛾量才显著小于性信息素的诱蛾量,OH的引诱力较弱。在河内,ACTE、NCS、OH第1天对小菜蛾引诱作用很强,引诱量大于性信息素,但差异不显著;随着诱芯放置时间延长,3种挥发物对小菜蛾的引诱量均下降很快,第4天的引诱力就很弱。3种植物挥发物的混合物(体积比1∶1∶1)对小菜蛾的引诱作用与性信息素相似,且诱蛾活性持效期相对较长。无论在越南或湖北,植物挥发物或其混合物均很少引诱到雌虫。     

小木蠹蛾性行为和性信息素产生与释放的时辰节律

观察了小木蠹蛾Holcocerus insularis的性行为反应,并采用腺体提取、空气收集 、触角电位和田间试验等方法对雌蛾产生和释放性信息素的时辰节律进行了研究。结果表明： (1) 该虫羽化24 h后性成熟,婚飞和交配活动主要在1：00～4：00,交配历时15～45 min;(2) 大部分雌蛾一生交配1～3次,雄蛾多数一生只交配1次,雌雄比为1∶0.89; (3) 雌蛾腺体提取物中性信息素含量同蛾龄有关,2日龄雌蛾腺体性信息素含量最高;(4) 雌蛾腺体中性信息素含量在1：00时最高,而性信息素释放高峰在2：30。     

Studies to evaluate the effectiveness of sex pheromone-impregnated formulations for control of populations of the American dog tick,Dermacentor variabilis (Say) (Acari: Ixodidae)

The sex pheromone, 2,6-dichlorophenol, was combined with a pesticide to control populations of the American dog tick,Dermacentor variabilis (Say). This pheromone persisted in the fur of treated dogs for at least 18 days. The mixture of pheromone and pesticide was much more effective in reducing mating among the surviving ticks than the treatments without pheromone. The pheromone-pesticide mixture also killed significantly more ticks than the treatment without pheromone. This increased effectiveness was due almost entirely to the significantly greater kill of male ticks. Combining the sex pheromone with pesticide treatments offers a means of suppressing tick populations by curtailing their mating and subsequent reproductive success. The potential applications of this technique and the benefits to be expected are discussed.     

Effect of age and mating on pheromone production in the female olive fruit fly, Dacus oleae (Gmel.)

Virgin female olive fruit flies began producing sex pheromone on the third day after emergence. Production of sex pheromone appears to be cyclical with peaks of production recurring at about 10-day intervals, each peak lasting 2–3 days. As the female ages, the quantity of sex pheromone produced during the period of high pheromone production decreases, but it is always higher than the quantity present in the pheromone gland during the rest of female life.Mated females produced less sex pheromone the first 10 days after mating which then increased to near the same level of that in virgin females.     

Role of the male claw sensilla in perception of female mounting sex pheromone in Dermacentor variabilis,Dermacentor andersoni and Amblyomma americanum

The foreleg claw sensilla of male D. variabilis, D. andersoni and A. americanum ticks indlude the receptors that perceive the female contact mounting sex pheromone (MSP). In all three tick species, the foreleg claw sensilla comprise six anteriorly-directed setae arranged in three symmetrical pairs, two each on the opposite sides of the apotele of the claw and one on the ventral side. Morphological study and behavioral bioassays of these setae revealed that only the dorsal and middle (=lateral) pairs of claw sensilla are mechanogustatory. While the ventral pair are strictly mechanoreceptors. The dorsal and middle sensory setae exhibit a single pore-like structure located at or near their tip, a feature characteristic of mechanogustatory sensilla. These setae are similar to those found on the palps that are believed to function as pheromone receptors. In all three tick species, male mounting and postmounting behaviors were suppressed only when the dorsal and middle pairs of claw sensilla were ablated or covered with gelatin; normal behavior was restored when the gelatin was removed. Doscresponse bioassays were conducted with D. variabilis males to authenticate the results of the gelatin tests. The results of these bioassays demonstrated that the gelatin coat was impervious to the pheromone. The characteristics of the ixodid tick mating system that distinguish it from mating processes in other arthropods are discussed.     

Circadian mating activity and effect of pheromone pre-exposure on pheromone response rhythms in the moth Spodoptera littoralis

Mating in moths is generally mediated by female-produced sex pheromones. Mating activity, female pheromone production/release and male pheromone responsiveness all show diurnal variations in many species. We found that the response of the male Egyptian cotton leafworm, Spodoptera littoralis, to sex pheromone gland extracts showed a diel rhythm in olfactometer tests, and the variation was persistent for at least 1 day in constant darkness. High male response to sex pheromone was correlated in time with high mating and locomotor activity. Male S. littoralis, maintained in constant darkness and exposed to pheromone gland extracts on a daily basis, showed an induced temporal variation in response after several days, in contrast to unexposed males. This suggests that in the absence of other external zeitgebers, exposure to sex pheromone may function to synchronise circadian behavioural rhythms in male moths. The daily rhythm in mating activity in S. littoralis is also shown to be persistent for at least 2 days in constant darkness. Pairs mated significantly less when either the male or female had been raised in a light:dark cycle 10 h out of phase, indicating that the proposed circadian rhythm in mating activity is composed of rhythmic mating preference/ability in both sexes.     

Inhibition of mating behaviour before feeding in the tick Aponomma hydrosauri

When on their host, both male and female adults of the reptile tick Aponomma hydrosauri require at least five days of feeding before normal mating behaviour will start. In off-host trials, fed females attract significantly more male contact than do unfed females, but unfed males show normal mating behaviour. All aspects of female mating behaviour are inhibited before feeding. Male mating behaviour has two stages: one comprises detachment and searching, the other, courtship behaviour. Only the former is inhibited before male feeding. This suggests the female signal has two components: one initiating searching, and the other initiating courtship. Males will always respond to the second component, but only after feeding will they respond to the first.     

Evidence for a mounting sex pheromone in the brown ear tick Rhipicephalus appendiculatus,Neuman 1901 (Acari: Ixodidae)

The presence of a mounting sex pheromone was demonstrated on the surface of fed female Rhipicephalus appendiculatus. This pheromone, which is present on the female cuticle, allows the male to recognise the female. The pheromone was removed by cleaning the female in hexane, resulting in the loss of male mating behaviour in in vitro experiments. Male mating behaviour was resumed when extract made from fed female cuticle was replaced on cleaned females. When the extract was transferred to innanimate objects typical male mating behaviour was released. Preliminary chemical analyses indicated that the active component of the extract was contained in the sterol ester fraction of the extract.     

Modelling female mating success during mass trapping and natural competitive attraction of searching males or females

Simulation models of insects encountering sex pheromone with or without mass trapping in which the searching sex is either male (moths and many insect species) or female (some true bugs, beetles, and flies) were developed. The searching sex moved as a correlated random walk, while the opposite sex remained stationary (calling) and released an attractive sex pheromone. The searching sex was caught when encountering a pheromone‐baited trap, and females mated when encountering a male. An encounter with pheromone was defined by the searcher's interception of a circle termed the effective attraction radius (EAR_c). Parameters of movement (speed and duration), initial numbers of calling sex and searching sex, number of traps, area, and EAR_c of traps and calling sex were varied individually to evaluate effects on the percentage of females mating. In the natural condition without traps, female mating success in both models was identical. Increasing the EAR_c of the calling sex caused diminishing increases in female mating success, suggesting that evolution of larger pheromone release and EAR_c is limited by increasing costs (production/sensitivity) relative to diminishing increases and benefits of mating encounters. With mass trapping, increasing the EAR_c of traps or density of traps caused similar declines in female mating in both models, but the female‐searching model predicted slightly lower mating success than the male‐searching model. Increasing the EAR_c of calling insects or the initial density of insects caused similar increases in female mating in both models, but again the female‐searching model had slightly lower mating success than the male‐searching model. The models have implications for mating lek formation and for understanding the variables affecting the success of mass trapping programs for insect pests with either male or female sex pheromones.     

Production and perception of pheromones by the beetle Tribolium confusum

Adults of Tribolium confusum secrete two pheromones. The first, produced by the male, is attractive to both sexes and the second, produced by the female, is attractive to the male only. Pheromone production and perception was studied in relation to habituation, beetle age, time of day and previous mating. A living source of each pheromone habituates the responding beetles, the male pheromone habituating more strongly; female pheromone habituates only in the absence of the male pheromone. Habituation to one pheromone was always accompanied by an enhanced response to the other.Five days after emergence, production of male pheromone reaches a peak that is maintained. Production of female pheromone peaks after 3 days. Both sexes are responsive to male pheromone immediately upon eclosion, males reaching maximum response at 14 days, females at 8 days. Males are also responsive to female pheromone upon eclosion reaching maximum response at 8 days; female response to female pheromone is imperceptible. Males but not females display a 24 hr rhythm in pheromone production. Mated beetles did not differ significantly from unmated beetles in their ability to perceive pheromones. Alteration in male pheromone production after mating was detected by females but not males; this pheromone may, therefore, act as both a sex and aggregation pheromone.