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成虫滞育的主要特点是生殖受到了抑制,其调控涉及到咽侧体、脑和前胸腺的作用,但主要以咽侧体的作用为主.滞育期间,咽侧体的活性很低,分泌的保幼激素量极微,而咽侧体的活性高低直接受脑所分泌的神经激素所调控. 相似文献
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家蚕蜕皮与变态的内分泌调控 总被引:2,自引:1,他引:2
家蚕的蜕皮与变态是由前胸腺分泌的脱皮素(molting hormone或 ecdysteroid简称 MH)及由咽侧体分泌的保幼激素(juvenile hormone)控制的,而促有前胸腺激素(prothoracicotropic hormone,以下简称PTTH)的功能为刺激前胸腺分泌蜕皮素。笔者近10年来从家蚕内分泌体系的一系列研究中发现,蜕皮素浓度的变化可以通过控制咽侧体的保幼激素的生物合成来影响幼虫发育,而PTTH的信息传递可通过调控前胸腺的功能,进而影响血淋巴中蜕皮素浓度。 相似文献
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刚羽化的淡色库蚊(Culex pipiens pallens)去首后,其第I卵泡停滞在N期,不能进一步发育。 5天以上日龄滞育蚊去首后,第I卵泡约在去首后24小时即从N期开始发育。 组织切片发现,滞育蚊咽侧体(CA)体积小,形态瘦长,略呈圆锥形,胞核着色深,排列紧密,胞质少,似处于失活状态。 滞育蚊卵巢转种到发育蚊体内,其卵泡可以发育,而转种到滞育蚊体内则不能发育。类保幼激素(JHA,ZR515)及从发育蚊血淋巴液中提取的粗制保幼激素都能使滞育蚊的卵泡发育。 相似文献
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南京地区棉铃虫越冬蛹滞育的解除与发育 总被引:8,自引:0,他引:8
南京地区棉铃虫Heliclverpa armigera (Hubner)越冬蛹滞育的解除时间及解除后发育与温度的关系等问题。结果表明,该地区越冬蛹于12月中旬前后解除滞育,12月下旬至3月上旬处于休眠状态,3月下旬至4月上旬温度上升至约10℃~12℃后眼点开始移动。发现该虫在滞育后的发育中,眼点移动前期的发育速率、发育起始温度及血淋巴总蛋白含量动态明显不同于眼点移动后期或非滞育蛹。 相似文献
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淡色库蚊生殖滞育的神经内分泌调节 总被引:2,自引:0,他引:2
刚羽化的淡色库蚊(Culex pipiens pallens)去首后,其第I卵泡停滞在N期,不能进一步发育。 5天以上日龄滞育蚊去首后,第I卵泡约在去首后24小时即从N期开始发育。 组织切片发现,滞育蚊咽侧体(CA)体积小,形态瘦长,略呈圆锥形,胞核着色深,排列紧密,胞质少,似处于失活状态。 滞育蚊卵巢转种到发育蚊体内,其卵泡可以发育,而转种到滞育蚊体内则不能发育。类保幼激素(JHA,ZR515)及从发育蚊血淋巴液中提取的粗制保幼激素都能使滞育蚊的卵泡发育。 相似文献
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丝带凤蝶滞育与非滞育蛹及其成虫的形态学观察 总被引:3,自引:0,他引:3
丝带凤蝶Sericinus montelus是一种有开发价值的观赏昆虫,以蛹滞育越冬,成虫存在多型现象。本研究从体色、个体大小和蛹腹部刺突长度等方面比较了丝带凤蝶滞育与非滞育蛹及其成虫的形态差异。与非滞育蛹相比,滞育蛹体色较深,触角末端的淡黄色与体色差异明显,3日龄滞育蛹腹部第9节刺突长度是3日龄非滞育蛹的4倍左右,这些差异可以用于该虫蛹滞育早期判别。滞育蛹羽化成虫的翅展和尾突长度显著小于非滞育蛹羽化成虫,且腹部及翅面斑纹也存在明显的差异,这些差异与丝带凤蝶春型、夏型成虫的描述相一致,表明丝带凤蝶成虫季节多型是与滞育相关联的。 相似文献
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烟夜蛾滞育蛹和非滞育蛹的耐寒性 总被引:1,自引:0,他引:1
对烟夜蛾Helicoverpa assultaGuen?e不同日龄滞育蛹和非滞育蛹的过冷却点和结冰点测定结果表明,在预蛹至5日龄蛹期,过冷却点和结冰点均逐渐下降。在预蛹期和3日龄蛹期,滞育蛹的过冷却点与非滞育蛹差异不显著;5日龄蛹时,滞育蛹和非滞育蛹的过冷却点分别下降至(-15.7±1.8)℃和(-13.5±1.2)℃,结冰点分别降至(-12.7±2.7)℃和(-9.5±1.3)℃,两类蛹间的差异均达极显著水平。自然越冬后,滞育蛹的存活率显著高于非滞育蛹,在土壤不同深处越冬的蛹的存活率存在差异,距土表15cm深的蛹存活率最高。 相似文献
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昆虫促前胸腺激素研究进展 总被引:4,自引:0,他引:4
昆虫促前胸腺激素研究进展李毅平龚和(中国科学院动物研究所,北京100080)关键词促前胸腺激素受体信号系统促前胸腺激素(prothoracicotropichor-monePTTH)因其促进前胸腺(PG)合成和分泌蜕皮激素而得名,以前也称为脑激素,因... 相似文献
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The imidazole derivative KK-42 is a synthetic insect growth regulator known previously to be capable of averting embryonic diapause in several Lepidoptera, but whether it also affects diapauses occurring in other developmental stages remains unknown. In the present study, we examined the effect of KK-42 on pupal diapause in two species of Lepidoptera, the Chinese oak silkworm Antheraea pernyi and the corn earworm Helicoverpa zea, and in one species of Diptera, the flesh fly Sarcophaga crassipalpis. In A. pernyi, KK-42 delayed pupal diapause termination under the long day conditions that normally break diapause in this species. Likewise, in H. zea, KK-42 delayed termination of pupal diapause, a diapause that, in this species, is normally broken by high temperature. KK-42-treated pupae of these two species eventually terminated diapause and successfully emerged as adults, but the timing of diapause termination was significantly delayed. KK-42 also significantly increased the incidence of pupal diapause in H. zea and S. crassipalpis when administered to larvae that were environmentally programmed for diapause, but it was not capable of inducing pupal diapause in H. zea if larvae were reared under environmental conditions that do not normally evoke the diapause response. Experiments with H. zea showed that the effect of KK-42 on pupal diapause was dose- and stage-dependent, but not temperature-dependent. Results presented here are consistent with a link between KK-42 and the ecdysteroid signaling pathway that regulates pupal diapause. 相似文献
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Regulation of host diapause by an insect parasitoid 总被引:1,自引:0,他引:1
SANDRA D. MOORE 《Ecological Entomology》1989,14(1):93-98
Abstract. 1. The interaction between larval development and parasitism by the braconid wasp Cotesia koebelei (Riley), was investigated in a population of the butterfly Euphydryas editha (Boisduval) (Nymphalidae). In this population, the butterfly host has an obligatory overwintering larval diapause.
2. It was found that E. editha larvae harbouring parasitoids were more likely to pass through an extra feeding instar before entering diapause than were non-parasitized conspecifics.
3. In addition, some individuals that were experimentally exposed to multiple parasitoid attacks bypassed diapause completely; these larvae passed through five or six feeding instars, reaching sizes typical of final instar post-diapause larvae.
4. The observed effect of superparasitism occurred regardless of whether the host larvae subsequently produced mature parasitoids, suggesting that parasitoid attack is sufficient to invoke the response.
5. It is proposed that the parasitoid C.koebelei regulates the number of pre-diapause feeding instars of its insect host E. editha, and that some component of the female venom, injected at oviposition, is responsible for this regulation. 相似文献
2. It was found that E. editha larvae harbouring parasitoids were more likely to pass through an extra feeding instar before entering diapause than were non-parasitized conspecifics.
3. In addition, some individuals that were experimentally exposed to multiple parasitoid attacks bypassed diapause completely; these larvae passed through five or six feeding instars, reaching sizes typical of final instar post-diapause larvae.
4. The observed effect of superparasitism occurred regardless of whether the host larvae subsequently produced mature parasitoids, suggesting that parasitoid attack is sufficient to invoke the response.
5. It is proposed that the parasitoid C.koebelei regulates the number of pre-diapause feeding instars of its insect host E. editha, and that some component of the female venom, injected at oviposition, is responsible for this regulation. 相似文献
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J Ilan 《The Journal of biological chemistry》1968,243(22):5859-5866
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Eco-physiological phases of insect diapause 总被引:4,自引:0,他引:4
Kostál V 《Journal of insect physiology》2006,52(2):113-127
Insect diapause is a dynamic process consisting of several successive phases. The conception and naming of the phases is unsettled and, sometimes, ambiguous in the literature. In this paper, the ontogeny of diapause was reviewed and the most often used terms and the best substantiated phases were highlighted, explained and re-defined. The aim was to propose relatively simple and generally applicable terminological system. The phases of diapause induction, preparation, initiation, maintenance, termination and post-diapause quiescence were distinguished. The specific progression through diapause phases in each species, population (genotype), or even individual, is based on (thus far largely unknown) physiological processes, the actual expression of which is significantly modified by diverse environmental factors. Thus, such phases are eco-physiological in their nature. 相似文献
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The effect of larval photoperiod on pupal colour and diapause in swallowtail butterflies 总被引:1,自引:0,他引:1
ABSTRACT.
- 1 There are significant differences in the effects of larval photo-period on diapause and pupal colour among the species Papilio polyxenes Fabr., P.troilus L., Battus philenor (L.) and Eurytides marcellus (Cramer).
- 2 Diapause and pupal colour in P.polyxenes and P.troilus are strongly influenced by larval photoperiod, short photophase eliciting brown diapausing pupae. Photoperiods of 15L:9D permit the expression of the green and brown pupal colour alternatives.
- 3 Pupal colour in B.philenor and E.marcellus is not affected by larval photoperiod, but short photophase induces diapause in these species.
- 4 All species except B.philenor show an association between brown pupal colour and diapause: Emarcellus when reared on long (midsummer) photophase, P.polyxenes and P.troilus when reared on short (autumnal) photophase.
- 5 In P.polyxenes, short photophase can affect pupal colour responses directly, whether the individual enters diapause or not.
- 6 Differences among the species are related to differences in the ecology of their natural pupation sites.