Pener M P
Department of Zoology, Hebrew University of Jerusalem, Israel.
Chronobiol Int. 1992 Apr;9(2):102-13. doi: 10.3109/07420529209064521.
Environmental cues, mostly photoperiod and temperature, mediated by effects on the neuroendocrine system, control reproductive diapause in female insects. Arrest of oocyte development characterizes female reproductive diapause, which has two major adaptive functions: It improves chances of survival during unfavorable season(s), and/or it confines oviposition to that period of the year that is optimal for survival of the eggs and progeny. Although reproductive diapause is less well studied in male insects, there may be no sex-dependent differences in regard to the first of these functions. The second one, however, is not valid for the male; instead, selection pressure directs the male's reproductive strategy toward maximum chances of fertilization of the female's eggs with minimum waste of energy. Therefore, in species with female reproductive diapause, the males may or may not exhibit diapause, but if they do, their diapause must be adapted to that existing in conspecific females. Male reproductive diapause is defined as a reversible state of inability of the male to inseminate receptive females. In relation to reproductive diapause, there are several patterns of coadaptations between male reproductive strategy and timing of female receptivity. (a) In some insects, the females are receptive in the early part of their diapause; mating occurs during this period and there is no diapause in the male. The male dies shortly after copulation and the female stores the sperms to fertilize the eggs that develop after termination of the female's diapause. (b) In some species, as in the grasshopper Anacridium aegyptium, females are receptive during diapause; though oocyte development is arrested, copulation occurs and the stored sperms fertilize the eggs when the female's diapause ends. Males were claimed to have no diapause, but recent studies have revealed the presence of a reproductive diapause in a proportion of the males. This and other cases show that female receptivity during reproductive diapause may or may not be accompanied by male reproductive diapause. If there is a reproductive diapause in the male, it is controlled by the same endocrine mechanism, the corpora allata (CA), as in the females. (c) In many species females are refractory during their diapause. In these cases, males exhibit reproductive diapause, which may be light, as in the beetle Oulema melanopus, or well established, as in certain grasshoppers, butterflies, and beetles. In the latter cases, male diapause is controlled by similar environmental cues (photoperiod, temperature) and by the same intrinsic mechanism (neuroendocrine system, especially CA) as female diapause.(ABSTRACT TRUNCATED AT 400 WORDS)
环境线索,主要是光周期和温度,通过对神经内分泌系统的影响发挥作用,控制着雌性昆虫的生殖滞育。卵母细胞发育停滞是雌性生殖滞育的特征,它具有两个主要的适应性功能:提高在不利季节存活的几率,和/或将产卵限制在一年中对卵和后代生存最适宜的时期。虽然雄性昆虫的生殖滞育研究较少,但就这些功能中的第一个而言,可能不存在性别差异。然而,第二个功能对雄性无效;相反,选择压力使雄性的生殖策略朝着以最小的能量浪费实现使雌性交配的卵子受精几率最大化的方向发展。因此,在具有雌性生殖滞育的物种中,雄性可能表现出滞育,也可能不表现出滞育,但如果表现出滞育,其滞育必须与同种雌性的滞育相适应。雄性生殖滞育被定义为雄性无法使处于接受状态的雌性交配的一种可逆状态。关于生殖滞育,雄性生殖策略与雌性接受期的时间之间存在几种协同适应模式。(a)在一些昆虫中,雌性在滞育早期具有接受能力;在此期间交配,雄性不存在滞育。雄性在交配后不久死亡,雌性储存精子以便在其滞育结束后发育的卵子受精。(b)在一些物种中,如埃及蝗,雌性在滞育期间具有接受能力;虽然卵母细胞发育停滞,但交配仍会发生,储存的精子在雌性滞育结束时使卵子受精。过去认为雄性没有滞育,但最近的研究表明一部分雄性存在生殖滞育。这一情况和其他例子表明,生殖滞育期间雌性的接受能力可能伴有也可能不伴有雄性生殖滞育。如果雄性存在生殖滞育,它与雌性一样受相同的内分泌机制,即咽侧体(CA)的控制。(c)在许多物种中,雌性在滞育期间不具有接受能力。在这些情况下,雄性表现出生殖滞育,这在一些物种中可能较轻,如黑背负泥虫,而在某些蝗虫、蝴蝶和甲虫中则较为明显。在后者的情况下,雄性滞育受与雌性滞育相似的环境线索(光周期、温度)和相同的内在机制(神经内分泌系统,尤其是咽侧体)控制。(摘要截选至400字)