小叶黑面神与小叶头细蛾互惠共生系统的种群调控机制(英文)

【目的】探索小叶黑面神Breynia vitis-idaea对小叶头细蛾Epicephala vitisidaea种群数量的调控机制。【方法】跟踪记录小叶黑面神物候及头细蛾的生物学。解剖在小叶黑面神上访花头细蛾的外生殖器,鉴定头细蛾种类。对不同时期小叶黑面神有梗和无梗的果实进行解剖,统计果实内幼虫数量、果实表面孔的数量以及果实表面产卵疤数量,计算头细蛾幼虫存活率。统计不同时期小叶黑面神有梗和无梗的果实的比例。【结果】在福建厦门小叶黑面神每年有5个花果期,相应地,为小叶黑面神传粉的头细蛾每年有5个生活世代。通过解剖,该种头细蛾被鉴定为小叶头细蛾。一头小叶头细蛾幼虫需要消耗2~4粒种子才能发育成熟。小叶黑面神有两种不同形态的果实:有梗和无梗。头细蛾幼虫在无梗果实内的存活率明显高于有梗果实,并且晚秋时期头细蛾幼虫的存活率要高于夏季。小叶黑面神无梗果实的比例在晚秋(82.04%)要高于夏季(31.53%)。【结论】本研究揭示了维持互利共生体系稳定的机制。小叶黑面神能够通过果实基部果梗的有无来调节小叶头细蛾幼虫的存活率。小叶黑面神通过季节性的调节有梗果实的比率,既有效避免了夏季种子被过度消耗的风险,又提高了头细蛾在冬季的存活率。小叶黑面神这种自身调控机制对维持小叶黑面神与小叶头细蛾互惠共生系统的稳定性起到了至关重要的作用。     

头细蛾专性授粉体系中区域性共生多样化研究

头细蛾属昆虫与叶下珠科植物互利共生体系中头细蛾复合体的区域性物种组成的具体情况是互利共生多样性研究模型选取的重要参考指标。本研究通过对全世界头细蛾属昆虫与叶下珠科植物协同进化体系中非一对一互利共生关系进行系统的整理,并对小果叶下珠Phyllanthus microcarpus、黑面神Breynia fruticosa、圆果算盘子Glochidion sphaerogynum、革叶算盘子Glochidion daltonii 4种植物相关的互利共生模式在不同分布区头细蛾物种成分以及种群动态进行研究。结果显示:在广西小果叶下珠居群上共生3种头细蛾,这3种头细蛾在同年的第一个世代只出现2种,在云南和海南小果叶下珠上全年只发现2种,而在广州目前饲养的头细蛾成虫更是仅有叔头细蛾1种;革叶算盘子在云南和四川有2种共生头细蛾,而在广西和海南均仅有1种;在海南和厦门黑面神与喙果黑面神共享2种头细蛾,而在广西和广东黑面神上仅发现1种头细蛾;圆果算盘子是目前发现共生头细蛾物种最复杂的寄主植物,在海南记载有4种头细蛾,但在云南圆果算盘子上仅发现优头细蛾1种。4种寄主植物相关的互利共生体系中头细蛾物种组成在不同的分布地均发生了不同程度的区域性共生多样化,甚至在同一地区的不同世代之间也存在着头细蛾物种数量的变化,这对于深入理解具有互利共生关系的物种间协同进化多样性形成机制具有重要的意义。     

中国头细蛾属昆虫(鳞翅目,细蛾科)与大戟科植物互利共生关系研究进展

细蛾科头细蛾属昆虫与大戟科算盘子属、叶下珠属和黑面神属植物互利共生关系的发现为研究昆虫与植物协同演化过程提供了一个全新的模式。目前,国内对头细蛾与大戟科植物的互利共生关系了解和研究都很少。本文介绍了头细蛾的分类、生物学和形态适应;大戟科相关5属植物(算盘子属、叶下珠属、黑面神属、白饭树属和守宫木属)的生物地理学,开花生物学,花的结构与传粉系统的关系;寄主植物与传粉者的对应关系;互利共生关系的维持机制等。研究表明中国有丰富的头细蛾与大戟科植物资源,开展其互利共生关系的研究有重要科学意义。很多新的、复杂的头细蛾与大戟科植物的生态关系和大量的头细蛾种类有待我们去发现和研究。     

叶下珠头细蛾与小果叶下珠互利共生的研究——生物学及系统稳定性

【目的】为了确定小果叶下珠Phyllanthus microcarpus与叶下珠头细蛾Epicephala sp.之间专性互利共生系统稳定性的增强是否主要通过彼此之间相互遏制对方对自身进行过度开采。【方法】通过对小果叶下珠上共生的叶下珠头细蛾形态及生物学的研究,记述了叶下珠头细蛾专性寄生寄主植物时的行为特性及共生双方利益得失。【结果】叶下珠头细蛾在广西一年两代,成虫的羽化数量与寄主植物雌雄花总数峰值变化同步;幼虫对小果叶下珠果实的寄生率为96%,单个果实内幼虫寄生数量1,但平均每个果实内被取食的种子为56.9%,叶下珠头细蛾低龄幼虫相对较高的死亡率限制了其对寄主种子的过度取食;果实内种子的适度保留和低龄幼虫的高死亡率是小果叶下珠-叶下珠头细蛾互利共生体系维持稳定的关键因素。【结论】小果叶下珠的表型性状出现了趋异性进化,叶下珠头细蛾与不同表型的小果叶下珠均有互利共生关系。因此,对叶下珠头细蛾形态及生物学进行详细研究有助于深入了解小果叶下珠与头细蛾共生体系物种组成多样性及进化生物学,并为探讨大戟科植物同头细蛾属昆虫协同互利共生多样性形成原因提供依据。     

叶下珠头细蛾与小果叶下珠互利共生的研究--生物学及系统稳定性

【目的】为了确定小果叶下珠 Phyllanthus microcarpus 与叶下珠头细蛾 Epicephala sp.之间专性互利共生系统稳定性的增强是否主要通过彼此之间相互遏制对方对自身进行过度开采。【方法】通过对小果叶下珠上共生的叶下珠头细蛾形态及生物学的研究,记述了叶下珠头细蛾专性寄生寄主植物时的行为特性及共生双方利益得失。【结果】叶下珠头细蛾在广西一年两代,成虫的羽化数量与寄主植物雌雄花总数峰值变化同步;幼虫对小果叶下珠果实的寄生率为96%,单个果实内幼虫寄生数量＞1,但平均每个果实内被取食的种子为56.9%,叶下珠头细蛾低龄幼虫相对较高的死亡率限制了其对寄主种子的过度取食;果实内种子的适度保留和低龄幼虫的高死亡率是小果叶下珠-叶下珠头细蛾互利共生体系维持稳定的关键因素。【结论】小果叶下珠的表型性状出现了趋异性进化,叶下珠头细蛾与不同表型的小果叶下珠均有互利共生关系。因此,对叶下珠头细蛾形态及生物学进行详细研究有助于深入了解小果叶下珠与头细蛾共生体系物种组成多样性及进化生物学,并为探讨大戟科植物同头细蛾属昆虫协同互利共生多样性形成原因提供依据。     

黑面神雌花气味传粉前后的变化及其生态意义

该文以与头细蛾传粉相关的叶下珠科植物黑面神为材料,采用动态顶空吸附法分别收集了该物种雌花传粉前后释放的挥发物,利用气相色谱-质谱联用技术分析了其化学成分,探索了三者间花气味的异同,并对其生态意义进行了讨论。结果表明:从该物种传粉前、传粉期和传粉后的雌花气味中共分离出22种挥发物(传粉前12种,传粉期15种和传粉后13种),以脂肪族衍生物和萜类物质为主。3-己烯醛、反-2-己烯醛、顺-3-己烯-1-醇、顺-乙酸-3-己烯酯、反-β-罗勒烯、β-石竹烯、β-蛇麻烯、反,反-α-金合欢烯和长叶烯是其主要挥发物。传粉前后雌花气味的化学种类及组成发生了显著分化,且这种变化主要是由于各时期主要挥发物发生改变而引起的。反-β-罗勒烯在传粉期含量最高,而在传粉后显著下降,3-己烯、反-2-己烯醛、顺-3-己烯-1-醇和顺-乙酸-3-己烯酯在传粉前含量均最高,β-石竹烯含量在传粉后显著升高,且长叶烯仅在传粉后出现。在传粉期和传粉后β-蛇麻烯和反,反-α-金合欢烯的含量均显著上升。同时,传粉期雌花的释放量明显高于传粉前和传粉后的。综上结果显示,黑面神雌花传粉前后花气味发生了质与量的改变。初步推测黑面神雌花传粉前后花气味的分化可能会有效阻止头细蛾对其进行再次访问,限制头细蛾在其雌花中过度产卵,进而来减少传粉头细蛾对宿主种子的取食,这无疑对维持叶下珠科植物-头细蛾专性传粉互利共生体系的稳定性具有重要的化学生态意义。     

三室算盘子寄主上弯头细蛾的生物学特性及花气味成分分析

【目的】为了从生物学和化学生态学角度探讨弯头细蛾Epicephala ancylopa和寄主三室算盘子Glochidion sp.间专性传粉的互利共生关系稳定性。【方法】本研究在野外观察和室内实验的基础上,对专性传粉育幼互利共生体系中三室算盘子、弯头细蛾生物学特性进行详细研究,探究互利共生双方利益得失;用动态顶空吸附法分别收集三室算盘子雄花和雌花气味物质,运用气相色谱-质谱联用技术(GC-MS)分析并鉴定其有效成分,用峰面积归一化与内标法定性定量;最后通过主成分分析法比较雄花和雌花之间气味化学成分的差异性。【结果】弯头细蛾在云南省普洱太阳河国家森林公园每年有1个世代,成虫和幼虫的活动时间分别在3-4月和8-10月。三室算盘子结实率为44.20%,被蛀食率为69.94%,平均每头幼虫消耗2.55枚种子来满足自身生长发育,寄主植物留有83.06%完好的种子,以维持互利共生关系的稳定。三室算盘子雌雄花气味中共鉴定出24种挥发物,主要以单萜类和倍半萜类物质为主,其中(Z)-罗勒烯和β-榄香烯两种萜类物质含量最高(分别为47.11%和22.72%),推测其是吸引弯头细蛾传粉的主要气味成分;雄花和雌花之间气味化学成分存在明显的差异,具有两性异型性。【结论】弯头细蛾通过以卵越夏和以蛹越冬对策,实现成虫发生期与三室算盘子花期的精准匹配。弯头细蛾成虫白天静伏,傍晚开始活动,三室算盘子花的气味物质也只在晚上才明显释放,且雌雄花气味化学成分的两性异型性有利于弯头细蛾辨别雌雄花,以完成采集花粉与传粉行为。该研究结果为头细蛾属昆虫与算盘子属植物专性传粉互利共生关系稳定性的维持机制提供了新的依据,也为深入开展通过触角电生理检测和生物行为实验来筛选吸引传粉头细蛾的活性物质提供了理论依据。     

优头细蛾(鳞翅目:细蛾科)的生物学特性及生存对策研究

【目的】探探索优头细蛾Epicephala sp.适应圆果算盘子Glochidion sphaerogynum特点而采取的生存对策,对揭示圆果算盘子与优头细蛾协同进化关系有重要的意义。【方法】本文通过对圆果算盘子物候、优头细蛾生活史、成虫活动规律以及圆果算盘子种子被幼虫蛀食情况这几方面的研究对优头细蛾适应性生存对策进行了探讨。【结果】圆果算盘子在整个算盘子属中呈现了一些与众不同的特点,特别体现在物候和雌花形态这两方面。在海南鹦哥岭,圆果算盘子每年只有一个花期,优头细蛾每年相应只有一个世代。优头细蛾是圆果算盘子的专性寄生者,承担着为圆果算盘子传粉的任务。头细蛾幼虫出果率为56.33%,完整种子保存率为56.58%,每头幼虫平均消耗4.53粒种子。【结论】优头细蛾通过以卵越夏对策,能够实现成虫发生期与圆果算盘子花期精准匹配。成虫选择了在雌花顶端小孔插入产卵器的产卵方式,并形成了与之相应的雌花选择和先产卵后传粉的生存对策,这样的产卵对策是适应圆果算盘子雌花形态的表现,同时对提高传粉效率、限制种子过度开采等方面体现了积极作用。     

革叶算盘子与两种头细蛾互惠共生体系的生物学研究

探索担头细蛾Epicephala duoplantaria和革叶头细蛾Epicephala daltonii共同为革叶算盘子Glochidion daltonii传粉的"一对二"协同进化模式。本文在野外观察和室内实验的基础上,对两种传粉头细蛾个体发育过程中生活习性和生活史进行详细研究并对比,记述共生双方利益得失;对比研究两种头细蛾幼虫形态特征的异同。结果表明,担头细蛾和革叶头细蛾在革叶算盘子上每年均为1个世代,幼虫和成虫的活动时间分别在2月-4月和4月-5月;革叶算盘子结实率为11.20%-27.02%,其中被蛀食率为26.47%-44.83%;果实中的种子败育率为26.03%-34.68%,种子被头细蛾蛀食率为9.29%-17.95%;平均每头幼虫消耗2.59-2.94粒种子来满足自身生长发育,每个植株留有49.53%-62.63%完好的种子,以维持互惠共生关系的稳定;产卵方式的差异导致担头细蛾的种群数量远高于革叶头细蛾;两种头细蛾的幼虫形态趋同进化但各自具有特性,这与革叶算盘子的形态特征及两种头细蛾习性有关。担头细蛾和革叶头细蛾共同为革叶算盘子传粉,形成了特殊的"一对二"协同进化互惠共生体系,推测担头细蛾是寄主转移来的传粉者,但该互惠共生体系并不稳定。     

危害黄杉球果的实小卷蛾属一新种(鳞翅目:卷蛾科)(英文)

记述了实小卷蛾属 (小卷蛾亚科 ,花小卷蛾族 )的一个新种 ,黄杉实小卷蛾RetiniapseudotsugaicolaLiuetWu ,sp .nov .。其幼虫危害黄杉PseudotsugasinensisDode的球果 ,在云南省禄劝县云龙乡球果受害率达 80 %～ 90 %。该新种雄性外生殖器的抱器瓣在腹面中央凹陷很深 ,抱器腹拐角几乎呈直角 ,抱器端的腹角尖 ,可与该属其它种相区别。该新种的雌性外生殖器与松实小卷蛾R .cristata很相似 ,但成虫的花纹完全不同 ,该新种前翅的中横带很宽 ,且布满了灰绿色和灰黄色的云状纹 ,而松实小卷蛾前翅的中横带则较窄 ,翅端有明显的肛上纹。在昆明禄劝县一年发生 1代 ,以蛹在球果中越冬。越冬蛹于翌年 3月下旬开始羽化。 4月上旬至 7月下旬是幼虫危害期。老熟幼虫 7月下旬开始陆续化蛹越冬。提供了成虫外形、翅脉、雌雄外生殖器解剖图及幼虫的毛序图。模式标本保存在中国科学院动物研究所     

Diffuse Coevolution between Two Epicephala Species (Gracillariidae) and Two Breynia Species (Phyllanthaceae)

The diffuse coevolution between two moth species (Epicephala lativalvaris and E. mirivalvata) and two plant species (Breynia fruticosa and B. rostrata) is reported based on field observations and indoor experiments conducted in Hainan and Fujian, China. Study results showed that the two Epicephala species jointly pollinated the two Breynia species, which led to a unique obligate pollination mutualism of two-to-two species specificity. A single Epicephala larva exclusively fed on seeds of host plants and developed to maturity by consuming all six seeds of each fruit, whereas a fraction of intact fruits were left to ensure the reproduction of plants within the whole population. Larvae of the two Epicephala species are competitive for resources; the population of E. mirivalvata is much smaller than that of E. lativalvaris, which has resulted from the differences in the female ovipositor structures and oviposition mode. The life history of Epicephala species highly coincides with the phenology of Breynia plants, and different phenology of B. fruticosa resulted in the different life history of the two Epicephala species in Hainan and Fujian. The natural hybridization of two host plants, possibly induced by the alternate pollination of two Epicephala species, is briefly discussed.     

Obligate pollination mutualism in Breynia (Phyllanthaceae): further documentation of pollination mutualism involving Epicephala moths (Gracillariidae)

This paper reports obligate seed-parasitic pollination mutualisms in Breynia vitis-idea and B. fruticosa (Phyllanthaceae). The genus Breynia is closely related to Glochidion and Gomphidium (a subgenus of Phyllanthus), in which pollination by species-specific, seed-parasitic Epicephala moths (Gracillariidae) have been previously reported. At night, female Epicephala moths carrying numerous pollen grains on their proboscises visited female flowers of B. vitis-idea, actively pollinated flowers, and each subsequently laid an egg. Examination of field-collected flowers indicated that pollinated flowers of B. vitis-idea and B. fruticosa almost invariably had Epicephala eggs, suggesting that these moths are the primary pollinators of the two species. Single Epicephala larvae consumed a fraction of seeds within developing fruit in B. vitis-idea and all seeds in B. fruticosa. However, some of the fruits were left untouched, and many of these had indication of moth oviposition, suggesting that egg/larval mortality of Epicephala moths is an important factor assuring seed set in these plants. The overall similarity of the specialized floral structure among Breynia species may indicate that this pollination system is fairly widespread within the genus.     

Evolution of obligate pollination mutualism in New Caledonian Phyllanthus (Euphorbiaceae)

About half a dozen obligate pollination mutualisms between plants and their seed-consuming pollinators are currently recognized, including fig-fig wasp, yucca-yucca moth, and the recently discovered Glochidion tree-Epicephala moth mutualisms. A common principle among these interactions is that the pollinators consume only a limited amount of the seed crop within a developing fruit (or fig in the case of fig-fig wasp mutualism), thereby ensuring a net benefit to plant reproduction. A novel obligate, seed-parasitic pollination mutualism between two species of New Caledonian Phyllanthus (Euphorbiaceae), a close relative of Glochidion, and Epicephala moths (Gracillariidae) is an exception to this principle. The highly specialized flowers of Phyllanthus are actively and exclusively pollinated by species-specific Epicephala moths, whose larvae consume all six ovules of the developing fruit. Some flowers pollinated by the moths remain untouched, and thus a fraction of the fruits is left intact. Additional evidence for a similar association of Epicephala moths in other Phyllanthus species suggests that this interaction is a coevolved, species-specific pollination mutualism. Implications for the evolutionary stability of the system, as well as differences in mode of interaction with respect to the Glochidion-Epicephala mutualism, are discussed.     

A non‐pollinating moth inflicts higher seed predation than two co‐pollinators in an obligate pollination mutualism

1. Mutualisms are relationships of mutual exploitation, in which interacting species receive a net benefit from their association. In obligate pollination mutualisms (OPMs), female pollinators move pollen between the flowers of a single plant species and oviposit eggs within the female flowers that they visit. 2. Competition between co‐occurring pollinator species is predicted to increase pollinator virulence, i.e. laying more eggs or consuming more seeds per fruit. Plants involved in OPMs frequently host various non‐pollinating seed parasites and parasitoids that may influence the outcome of the mutualism. Quantifying the prevalence of parasites and parasitoids and competition between pollinators is important for understanding the factors that influence OPM evolutionary stability. 3. This study investigated the pollination mutualism occurring between the leaf flower plant, Breynia oblongifolia, and its co‐pollinating Epicephala moths. A third moth, Herpystis, also occurs in B. oblongifolia fruits as a non‐pollinating seed parasite. 4. Breynia oblongifolia fruits were collected to quantify seed predation and compare seed predation costs between the three moth species. Results showed that the larvae of the two pollinator species consume similar numbers of seeds, and that adults deposit similar numbers of eggs per flower. As such, no evidence of increases in virulent behaviours was detected as a result of competition between co‐pollinators. 5. By contrast, the seed parasite Herpystis consumed more seeds than either pollinator species, and fruit crops with a high proportion of Herpystis had significantly lower net seed production. 6. This work adds to the growing understanding of the ecology and dynamics of plant–pollinator mutualisms.     

Evolution of obligate pollination mutualism in the tribe Phyllantheae (Phyllanthaceae)

The landmark discovery of obligate pollination mutualism between Glochidion plants and Epicephala moths has sparked increased interest in the pollination systems of Phyllantheae plants. In this paper I review current information on the natural history and evolutionary history of obligate pollination mutualism in Phyllantheae. Currently, an estimated >500 species are mutualistic with Epicephala moths that actively pollinate flowers and whose progeny feed on the resulting seeds. The Phyllantheae also includes species that are not mutualistic with Epicephala moths and are instead pollinated by bees and/or flies or ants. Phylogenetic analyses indicate that the mutualism evolved independently five times within Phyllantheae, whereas active pollination behavior, a key innovation in this mutualism, evolved once in Epicephala . Reversal of mutualism has occurred at least once in both partner lineages, involving a Breynia species that evolved an alternative pollination system and a derived clade of Epicephala that colonized ant-pollinated Phyllantheae hosts and thereby lost the pollinating habit. The plant–moth association is highly species specific, although a strict one-to-one assumption is not perfectly met. A comparison of plant and moth phylogenies suggests signs of parallel speciation, but partner switches have occurred repeatedly at a range of taxonomic levels. Overall, the remarkable species diversity and multiple originations of the mutualism provide excellent opportunities to address many important questions on mutualism and the coevolutionary process. Although research on the biology of the mutualism is still in its infancy, the Phyllantheae– Epicephala association holds promise as a new model system in ecology and evolutionary biology.     

传粉细蛾与大戟科植物专性授粉的互惠共生体系

在已知的昆虫与植物所形成的专性授粉互惠共生体系中,榕树—榕小蜂、丝兰—丝兰蛾体系是经典实例,国内外学者已经从不同角度进行了大量的研究,为我们理解植物—传粉者互惠共生体系协同进化的机理和历史积累了宝贵的资料。近些年的研究发现鳞翅目细蛾科头细蛾属昆虫与大戟科植物之间也存在相似的协同进化关系。文章对国内外学者有关传粉细蛾与大戟科植物互惠共生协同进化的研究进行了整理。     

The Mutual Adaption Between the Ovipositor of <Emphasis Type="Italic">Epicephala eriocarpa</Emphasis> and the Style of <Emphasis Type="Italic">Glochidion eriocarpum</Emphasis>

Specialization of adaptive devices can reflect the coevolution of closely interactive relationship between partners in mutualism. Glochidion eriocarpum and Epicephala eriocarpa have formed a strict species-specific mutualism over a long term of evolution. Based on field observation and the anatomical study of adult specimens, we clarified the morphological and biological characteristics of E. eriocarpa and performed morphological analyses of the specialized female genitalia for the first time. Epicephala eriocarpa had four generations per year. Adaptive specialization in the mutualism was expressed by morphological variations in the relative length of the ovipositor and the flower style. The mean length of the apophyses posteriores, which constituted 38% of E. eriocarpa body size, was unique among known Epicephala species. The variations among partners suggested that the flower style might have selected an optimal ovipositor length in its pollinator. This indicated that highly specialized structures resulted from mutual specificity and reciprocal adaptation among interacting partners in “one-to-one” mutualism. The evolutionary characteristics of pollinators might be more sensitive to outside stimulation than their partners and could express the process of adaptive evolution better. Moreover, our analyses help to further understand the evolutionary mechanism and driving force of cospeciation in obligate pollination mutualism.     

Repeated independent evolution of obligate pollination mutualism in the Phyllantheae-Epicephala association

The well-known fig-fig wasp and yucca-yucca moth mutualisms are classic examples of obligate mutualisms that have been shaped by millions of years of coevolution. Pollination systems involving obligate seed parasites are only expected to evolve under rare circumstances where their positive effects are not swamped by abundant co-pollinators and heavy costs resulting from seed destruction. Here, we show that, in Phyllantheae, specialization to pollination by Epicephala moths evolved at least five times, involving more than 500 Phyllantheae species in this obligate association. Active pollination behaviour evolved once in Epicephala, 10-20 Myr after the initial divergence of their host plants. The pollinating Epicephala moths thus radiated on an already-diverged host lineage and successively colonized new Phyllantheae hosts, thereby giving rise to repeated independent evolution of the specialized pollination system in Phyllantheae. The present evolutionary success of this association rests entirely upon active pollination by Epicephala, making this a distinct example of an evolutionary key innovation. Overall, our findings provide a clear empirical demonstration of how a combination of evolutionary innovation and partner shifts facilitates the spread of mutualism in a coevolving species interaction.     

西藏飞蝗的生物学特性

西藏飞蝗Locusta.migratoria tibetensis Chen在四川甘孜州1年发生1代,某些地方(乡城县)1年发生不完整的2代,即以卵越冬,翌年3月下旬开始孵化出土,4月中、下旬为孵化盛期,1~3龄始盛期为4月中旬~5月中旬,高峰期为5月下旬,7月上旬初始羽化,7月下旬~8月上旬为羽化盛期,8月上旬始见产卵,8月下旬~9月上旬为产卵盛期,第1代成虫较早产下的卵块在条件适宜的情况下可于当年9月上旬孵化出土,但孵化出的蝗蝻不能越冬。该虫卵、全蝻期及全世代的发育起点温度分别为14.2,16.1,14.6℃,有效积温为179.1日.度、360.0日.度、787.8日.度。在18,21,24,27和30℃等5种恒温条件下其平均世代历期214.4,133.3,79.2,66.3和50.7d。