枣镰翅小卷蛾性信息素通讯系统

采用单个雌蛾性信息素腺体分析技术对枣镰翅小卷蛾Ancylis sativa Liu雌蛾性信息素的组分和组分间的精确比例进行了测定,结果表明,枣镰翅小卷蛾雌蛾的性信息素系统由二个顺反异构体组分组成,即反-9-十二碳烯醋酸酯(E9-12∶Ac)和顺-9-十二碳烯醋酸酯(Z9-12∶Ac)组成,E9-12∶Ac与Z9-12∶Ac的比例为6.5∶3.5;雌蛾产生和释放性信息素具有时辰节律性,在光周期14L∶10D、温度为21℃时,性信息素产生的高峰期为进入黑暗期6.5 h;不同日龄雌蛾产生的性信息素有差异,1日龄最低,2日龄最高,3～5日龄居中,不同日龄雌蛾产生的性信息素组分间的比例无显著差异;对3个世代雌蛾产生的性信息素的量及组分间的比例的研究表明,越冬代含量最高,为(10.1±7.0)ng/头,第2代为(9.5±4.6)ng/头,第1代仅为(1.4±1.0)ng/头,3个世代性信息素组分间的比例无显著差异,在63.1%～64.3%(E)范围内。     

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.     

Mating Effect on Sex Pheromone Production of the Oriental tobacco budworm,Helicoverpa assulta

This study was undertaken to clarify the suppression phenomenon of sex pheromone production after mating and its relationship to the physiological mechanism in adult females of Helicoverpa assulta, and determine the mating factor from males causing depletion of sex pheromonc production. Sex pheromone production of H. assulta females was mostly terminated in 3 hours after mating. Mated females maintained with a low titer of sex pheromone until 3 days when it started to increase again, which showed a characteristic of species mating more than once. The mated female again produced pheromone upon injection of pheromone biosynthesis activating neuropeptide (PBAN) or extracts of brain-suboesophageal ganglion complexes (Br-Sg) of mated female, which were shown similar pheromonotropic activities as compared with virgin females. These results indicated that the mating did not inhibit the receptivity of pheromone gland itself and PBAN biosynthesis in suboesophageal ganglion of the mated females. And it seems to support that the depletion of sex pheromone production is responsible for blocking of PBAN release from head. To investigate the mating factor from adult males, when extracts of reproductive organs of male were injected into hemocoel of virgin females evoking depletion of sex pheromone production as shown in mated female. The results suggest that a chemical substance(s) from the male reproductive organs could be responsible for the loss of sex pheromone biosynthesis in H. assulta.     

Sex pheromone titre in the glands of Spodoptera litura females: circadian rhythm and the effects of age and mating

The present study investigates the effects of age and mating status on the circadian variations of gland sex pheromone titre in female Spodoptera litura Fabricius. Similar to other nocturnal moths, S. litura females exhibit circadian variations of gland sex pheromone contents, with higher levels during scotophase and lower levels during photophase. The sex pheromone titre in the glands peaks during the first scotophase after eclosion and sharply declines afterwards. Higher pheromone contents during scotophase may facilitate female reproductive activities, and the negative relationship between pheromone titre and female calling is likely the result of pheromone release during female calling. Interestingly, the present study demonstrates that mated S. litura females have significantly higher sex pheromone titre in their pheromone glands (PGs) than virgin females. This finding contrasts with all previous studies of other insect species, in which mating generally reduces the sex pheromone titre in female PGs. In S. litura, mating and male accessory gland fluids can suppress female calling behaviours and re‐matings. These results suggest that the suppression of female calling behaviours by mating and male accessory gland fluids may significantly reduce the release of sex pheromones and thus result in higher sex pheromone titre in the PGs of mated females.     

Endocrine regulation of female contact sex pheromone production in the German cockroach, Blattella germanica

ABSTRACT The amount of the major component of the cuticular sex pheromone, 3, 11-dimethyl-2-nonacosanone, on individual female German cockroaches, Blattella germanica (L.), as a function of age was determined by gas-liquid-chromatographic analysis. Accumulation of phermone increased with age in both virgin and mated females. During the first gono-trophic cycle, the pheromone accumulated most rapidly when oocyte growth rates were maximal (days 5–10), and least rapidly while the female carried an ootheca (days 11–32). Pheromone accumulation was similar in virgin and mated females when the same physiological stages (determined by oocyte maturation) were considered. Inhibition of Juvenile Hormone release, through allatectomy, chemicals (precocene or fluoromevalonate), or through mechanical egg case implants, suppressed or delayed pheromone production and oocyte growth. The Juvenile Hormone analogue ZR512 induced allatectomized or head-ligated females and females with chemically or mechanically inhibited corpora allata to produce pheromone and enlarge their basal oocytes. Finally, ZR512 applied to intact females stimulated pheromone production in a dose-dependent manner.     

蜀柏毒蛾生殖行为及性信息素产生与释放节律

为了探索蜀柏毒蛾Parocneria orienta Chao性信息素产生和释放规律, 为利用性信息素监测和防治蜀柏毒蛾奠定基础, 本研究在野外及室内温度22±1℃、 相对湿度75%~80%、 光周期14L∶10D条件下观察研究了蜀柏毒蛾成虫的羽化、 求偶、 交尾、 产卵行为, 触角电位反应测定处女雌蛾性信息素产生与释放的时辰节律。结果表明： 蜀柏毒蛾羽化行为全天可见, 主要集中在1:00-5:00, 占总羽化量的44.94%, 7:30-11:00进行婚飞和交尾, 交尾高峰期出现在8:30左右, 交配时间少则2 h, 多则8 h, 求偶、 交配均发生在光期。随着日龄的增加, 召唤时间前移并且延长, 1日龄的处女雌蛾交尾时间较短; 雌蛾羽化当天就可交尾, 2日龄雌蛾交尾率最高, 达36.67%。雌蛾分多处产卵, 雌蛾一生最高产卵量达402粒, 最低产卵量为78粒。羽化当天的雌蛾体内性信息素含量较低, 第2天最高, 以后逐日下降; 2日龄蜀柏毒蛾处女雌蛾性信息素的产生量从7:00起逐渐增加, 8:30-9:30时最高, 9:30后逐渐减小。雄蛾对处女雌蛾腺体提取物的触角电位反应在8:30-9:00最强, 说明8:30-9:00是雌蛾产生和释放性信息素的高峰期。蜀柏毒蛾的羽化、 求偶、 交尾及性信息素的产生与释放存在一定的时辰节律, 野外处女雌蛾诱蛾试验证实了性信息素释放与交配行为在时辰节律上的一致性。     

Effects of decapitation and PBAN injection on amounts of triacylglycerols in the sex pheromone gland of Manduca sexta (L.)

The correlation between triacylglycerols containing conjugated diene fatty acyl moieties and pheromone aldehydes in the sex pheromone glands of females of Manduca sexta was investigated. Females decapitated 15 h after adult emergence neither called nor produced pheromone during the natural period of pheromone production on the subsequent two nights. However, these females could be stimulated to produce sex pheromone for prolonged periods by repeated injection of synthetic pheromone biosynthesis activating neuropeptide (PBAN). Gas chromatographic analysis of methanolysis products of lipids extracted from the pheromone glands of decapitated and intact females showed no differences in the amounts of fatty acyl precursors of pheromone. High performance liquid chromatographic analysis of the triacylglycerols containing conjugated diene analogues of the pheromone components (diene TG), obtained 24 and 48 h after decapitation, showed that the total amounts of these components were not affected by decapitation. The amounts of all diene TG peaks declined significantly when decapitated females were stimulated to produce pheromone during a 7 h period by repeated injection of PBAN at 3 h intervals but recovered when pheromone production subsided. These results indicate that PBAN induces liberation of pheromone precursors from the triacylglycerols during pheromone biosynthesis but does not induce replenishment of this storage pool. © 1996 Wiley-Liss, Inc.

1 This article is a US Government work and, as such, is in the public domain in the United States of America

     

Grasshopper sexual pheromone: a component of the defensive secretion in Taeniopoda eques

ABSTRACT. Both male and female Taeniopoda eques (Burmeister) emit a defensive secretion from their thoracic spiracles. The secretion from mature females was found to act as a sex pheromone, eliciting mating behaviour in males. Females became chemically attractive to males about 16–18 days after eclosion. The antennae are shown to be the site of pheromone reception in males. Feeding upon natural host plants was not a prerequisite for pheromone production.     

Termination of sex pheromone production in mated females of the silkworm moth

A mating duration of more than 6 h was necessary to permanently terminate the production of the sex pheromone (bombykol) in the silkworm moth, Bombyx mori L. (Lepidoptera: Bombycidae), although the female formed a bursa copulatrix including a spermatophore and laid fertilized eggs even after mating for only 0.5 h. The 6-h mated female again produced bombykol if given an injection of synthetic pheromonotropic neuropeptide (PBAN), which is known to activate pheromone biosynthesis in a virgin female. Extracts of brain-suboesophageal ganglion (SG) complexes, which were removed from 6- and 24-h mated females, showed strong pheromonotropic activities. These results indicated that the pheromone gland of the mated female maintained its ability to biosynthesize bombykol; however, it could not produce pheromone due to a suppression of PBAN secretion from the SG. Furthermore, bombykol titers did not decrease after mating in females with a transected ventral nerve cord, even after the injection of a spermatophore extract, suggesting that the suppression of PBAN secretion was mediated by a neural signal and not by a substance in the spermatophore. The mated females accumulated (10E, 12Z)-10,12-hexadecadienoic acid, a precursor of bombykol biosynthesis, in their pheromone glands as did decapitated females. © 1996 Wiley-Liss, Inc.     

Periodicity of pheromone release from female white peach scale

ABSTRACT The sex pheromone of the female white peach scale, Pseudaulacaspis pentagona (Targioni-Tozzetti), is released by newly-mature females to correspond with the daily eclosion rhythm of males. As with male eclosion, pheromone release commences relative to the onset of light and is suppressed by increasing temperature. Once pheromone release begins it is maintained until the initiation of the scotophase. Pheromone release does not occur during the scotophase. When sexually mature females remain unmated for 5 days, the release of pheromone begins earlier in the day than it does with newly mature females.     

Electrophysiological investigations of sex pheromone reception and release in Bruchidius atrolineatus

ABSTRACT. Male antennal sensitivity to female sex pheromone in Bruchidius atrolineatus was investigated electrophysiologically (EAG). The existence of receptors for this pheromone was shown in the antennae of males. (No such receptors exist in the antennae of females.) Young (age < 24h) males gave an EAG of amplitude 25–30% of the response of older males. Diapausing males several days old gave a much smaller response than active males of the same age.
EAGs were used to test the production/release of pheromone by groups of twenty females. Before they are 24 h old, active females do not produce/release the pheromone; older females release it at an almost constant rate. Sexually diapausing females do not produce and/or release the sex pheromone.
In sexually active females, mating inhibits pheromone release almost immediately. There is a correlation between reproductive status of the females (development of ovaries, oogenesis) and the production or release of the pheromone. A corresponding correlation also exists in the males whose antennae show a very low sensitivity when they are young or when they are in reproductive diapause.     

PBAN regulation of pheromone biosynthesis in female tobacco hornworm moths,Manduca sexta (L.)

Manduca sexta females that were decapitated produced no pheromone during the scotophase following decapitation, indicating that they were free of pheromone biosynthesis activating neuropeptide (PBAN). When deuterated hexadecanoic or (Z)-11-hexadecenoic acid was applied to the sex pheromone glands of decapitated or intact females of the same age, and allowed to incubate in vivo for 24 h, deuterium labeled Δ-11- and Δ-10, 12-unsaturated 16-carbon fatty acids were produced in both types of females. Injection of PBAN into intact or decapitated females 23 h after application of labeled acids had no effect on the production of unsaturated labeled fatty acids. However, deuterium labeled aldehydes were produced only in females that were injected with PBAN. Therefore, in this species, PBAN activates the process by which fatty acyl precursors in the pheromone gland are converted into the pheromonal aldehydes. © 1995 Wiley-Liss, Inc.

1 This article is a US Government work and, as such, is in the public domain in the United States of America.

     

Electrophysiological and Behavioral Responses of Female Beet Armyworm Spodoptera exigua (Hübner) to the Conspecific Female Sex Pheromone

Electroantennogram (EAG) recordings showed that female Spodoptera exigua can detect their own sex pheromones (two single components and their mixture), displaying a similar dose–response pattern to that of males, although intensities of female responses were much less at all doses compared with males. Furthermore, the female calling behavior was inhibited and late-shifted by the presence of the female sex pheromone. When the pheromone components were presented, the calling female proportion in the peak calling period was significantly reduced and the calling peak time and calling termination time postponed, compared with controls. Although the calling behavior was inhibited, the pheromone titer of treated females was not different to the control, implying a reduced pheromone biosynthesis in the pheromone glands of treated moths. However, observations during the olfactometer experiments revealed that there were no obvious behavioral responses of females exposed to sex pheromone stimuli including whole gland extracts, 0.1, 1 or 10 μg binary pheromone mixtures.     

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。     

Sex pheromone-releasing behaviour in females of the dermestid beetle,Trogoderma glabrum

Adult Trogoderma glabrum females assume stationary postures characterized by abdominal elevation and partial exposure of the ovipositor segments. The postural activity was studied in relation to sex pheromone production and was designated calling, or sex pheromone-releasing behaviour because it was accompanied by an increase in the rate of release of sex pheromone(s). Calling was largely restricted to an 8 hr interval centered toward the middle of a 16 hr photophase. Mating frequency and female pheromone content increased during the same interval. Because females extracted during the calling period yielded at least 10 times more pheromone than extracts prepared at other times, and because pheromone activity released during one calling period was estimated to be at least 10-fold higher than that which could be extracted from whole females several hours prior to the start of calling, heightened production of active pheromone(s) was postulated to occur during calling. Functional significance of the calling posture is discussed in relation to sex pheromone gland location.     

Drosophila melanogaster sex peptide stimulates juvenile hormone synthesis and depresses sex pheromone production in Helicoverpa armigera

Previous studies demonstrate that virgin female adult Helicoverpa armigera (Lepidoptera: Noctuidae) moths exhibit calling behaviour and produce sex pheromone in scotophase from the day after emergence, and that mating turns off both of these pre-mating activities. In the fruit fly Drosophila melanogaster, a product of the male accessory glands, termed sex peptide (SP), has been identified as being responsible for suppressing female receptivity after transfer to the female genital tract during mating. Juvenile hormone (JH) production is activated in the D. melanogaster corpus allatum (CA) by SP in vitro. We herein demonstrate cross-reactivity of D. melanogaster SP in the H. armigera moth: JH production in photophase virgin female moth CA in vitro is directly activated in a dose-dependent manner by synthetic D. melanogaster SP, and concurrently inhibits pheromone biosynthesis activating neuropeptide (PBAN)-activated pheromone production by isolated pheromone glands of virgin females. Control peptides (locust adipokinetic hormone, AKH-I, and human corticotropin, ACTH) do not inhibit in vitro pheromone biosynthesis. Moreover, SP injected into virgin H. armigera females, decapitated 24 h after eclosion, or into scotophase virgin females, suppresses pheromone production. In the light of these results, we hypothesize the presumptive existence of a SP-like factor among the peptides transmitted to female H. armigera during copulation, inducing an increased level of JH production and depressing the levels of pheromone produced thereafter.     

褛裳夜蛾的交配行为及雄蛾对性腺提取物的反应节律

详细观察了褛裳夜蛾成虫的交配行为,利用风洞、触角电位技术研究了雄蛾对性腺提取物的反应节律,通过林间诱蛾试验进行了验证,旨在为褛裳夜蛾性信息素的精确提取及性信息素组份分离、鉴定提供依据。研究结果表明:成虫的求偶、交配行为均发生在暗期,有一定的节律性:雌蛾在羽化3d以后开始求偶,1周左右表现最为强烈,3-4日龄雌蛾在暗期4-6h开始求偶,最大求偶率在暗期6-8h;5-9日龄在进入暗期就开始求偶,最大求偶率出现在暗期4-6h。风洞试验表明,3-7日龄的雄蛾对性腺提取物均有明显的性行为反应,5日龄雄蛾在暗期4-6h对性腺提取物的反应最为强烈。3-6日龄的成虫在暗期4-6h开始交配,而7-8日龄的成虫于暗期2-4h开始交配,6日龄的成虫交配率最高,交配高峰在暗期4-8h。雄蛾对性腺提取物的触角电位反应也有一定的节律性:雄蛾对4日龄雌蛾性腺提取物开始有电生理反应,对6-7日龄暗期5h性腺提取物反应最为强烈。林间诱蛾试验测定了性腺提取物的引诱活性,7日龄雌蛾性腺提取物林间诱蛾量最高,引诱高峰在暗期4-6h,该结果也验证了褛裳夜蛾雄蛾对性腺提取物的反应节律。     

Ultrastructural changes associated with pheromone production in the sex pheromone gland of Diatraea saccharalis

An ultrastructural study of the sex pheromone gland of female adult sugarcane borers suggests that pheromone is not produced during the first 2 hr after emergence but reaches a peak 48 hr after emergence. The sex pheromone gland is composed of two cell types and a number of structural changes observed to occur in the cells of the sex pheromone gland prior to pheromone production are described.     

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。     

Calling Behavior and Rhythms of Sex Pheromone Production in the Black Cutworm Moth in China

The hourly and daily variation of calling behavior and sex pheromone production by the female black cutworm moth, Agrotis ypsilon (Rottemberg), were investigated. Both calling behavior and titers of five sex pheromone components showed distinct diel rhythms, and peak periods of calling and pheromone titer were synchronous. Females began to call on the first night after eclosion and called mainly during the second half of the scotophase. The percentage of females calling increased in 1 to 3-d-old females and decreased in 3 to 7-d-old females. Females advanced their calling time with increasing age (1 to 7 d). GC-MS analysis of hexane extracts of pheromone glands revealed that the titers of the five sex pheromone components were very low on the first night after eclosion, but increased sharply and peaked on the third night. Titers decreased greatly with increasing age (3 to 7 d), but from the onset of the scotophase to 4.5 h into scotophase, titers remained invariate. However, from 4.5 to 7 h, pheromone titers, especially that of the primary component Z7-12:Ac, increased sharply and peaked. After the peak, the titers decreased greatly at 8 h, and thereafter decreased gradually to the level before 4.5 h. The quantity of each component almost reached zero after lights-on.