Cultural Entomology

B. Morris
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引用次数: 29

Abstract

he long-range female-attracting songs and long tactual cerci °r crickets are components of a unique mating system, some aspects of which evidently trace to the earliest instances of copulation in the insect line and help explain changes leading to 'he current major groups of insects. Thus, none of the primitively wingless modern insects copulate, while all winged >d secondarily wingless insects do, the majority with the male mounting the female and in some way holding or forcing her. n primitively wingless insects, however, a sac or bulb containing the sperm (a spermatophore) is transferred indirectly to the female without direct copulation. Like crickets, some ol these particular primitively wingless insects possess prominent tactual cerci (e.g., Thysanura), used to guide the female during spermatophore transfer, as also in cockroaches and mayflies, n all insect groups of ancient origin that have prominent tactual cerci, transfer of the spermatophore is a luring act in which the female either mounts (winged and secondarily ngless forms) or stands beside the male (primitively wingless s). In some crickets, such as the field cricket genus Gryllus, copulatory act appears unique among all animals in being entirely luring, with no evidence of controlling force by the e at any stage. The female' is .ittraded initially by the longange calling song and then by the male's close-range courtship ;°g and probably the fluttering touches of his antennae 'g7). As in nearly all crickets, most close relatives of crickets, and most cockroaches and mayflies (the last aerially), the ale mounts (or flies above) the male in the copulatory act. PParently in correlation with the male field cricket having nimal ability to clasp the females genital parts, the Prnatophore is transferred quickly, in 15 to 90 s. The 'ermatophore is osmotically self-emptying, so that sperm lection occurs largely after the female dismounts from the In forms related to crickets, such as Tettigoniidac and fera, m which males have evolved terminal claspers on the nen, the tactual cerci have disappeared and copulation rnucn lengthier. In Caelifera the mating act has evolved c that the male mounts the female, though still reaching neath her to attach the genitalia; here, un l ike Tettigoniidae, ntennae have also become much shorter. Apparently S copulatory acts in insects have repeatedly evolved into acts involv ing s igni f ican t force, but the reverse does not seem to have happened. Groups of features related to the history of insect mating acts have significance for interpreting changes in diagnostic features of major groups of insects, including cerci, . in tennae, gcn i t a l i a , wing structure, long-range communication, and modes of pair formation. Distinctive morphological and behavioral features of crickets, especially those related to their methods of pair formation and mating behavior, make them a pivotal group in understanding insect evolution and phylogeny.
文化昆虫学
蟋蟀长距离的吸引雌性的歌声和长触角是独特交配系统的组成部分,其中一些方面显然可以追溯到昆虫系中最早的交配实例,并有助于解释导致“当前主要昆虫群体”的变化。因此,没有一种原始的无翅现代昆虫交配,而所有有翅的>d次无翅昆虫交配,大多数是雄性骑在雌性身上,以某种方式抓住或强迫她。然而,在原始的无翅昆虫中,含有精子(精子包囊)的囊或球被间接地转移给雌性,而不直接交配。像蟋蟀一样,一些原始的无翅昆虫拥有突出的触须(例如,袋尾虫),用于引导雌性在精子包囊转移过程中,蟑螂和蜉蝣也是如此。在所有具有突出触须的古代昆虫群体中,精子包囊的转移是一种诱惑行为,雌性要么骑上(有翼的和次级无翼的形式),要么站在雄性(原始无翼的形式)旁边。如田蟋蟀属,交配行为在所有动物中似乎是独一无二的,完全是引诱,没有证据表明在任何阶段都有控制力量。雌鸟最初是用长音鸣叫来交换的,然后是雄鸟近距离的求爱(可能还有它触须的抖动)。就像在几乎所有的蟋蟀、蟋蟀的近亲、大多数蟑螂和蜉蝣(最后一种空中昆虫)中一样,雄性在交配时骑在雄性身上(或飞在上面)。显然,与雄性蟋蟀具有动物般的抓住雌性生殖器的能力有关,Prnatophore在15到90秒内转移得很快。生殖细胞具有渗透性的自掏空作用,因此,精子的选择主要发生在雌性从与蟋蟀相关的雄性(如蟋蟀和fera)中分离出来之后,雄性在雄性身上进化出了末端扣环,触须消失,交配时间延长。在Caelifera中,交配行为已经进化成雄性骑在雌性身上,尽管它仍然会伸到雌性的身下附着生殖器;这里,不像扇甲科,触角也变得更短了。很明显,昆虫的交配行为已经反复进化为涉及到力的行为,但相反的情况似乎并没有发生。与昆虫交配行为历史相关的特征群对于解释主要昆虫类群的诊断特征变化具有重要意义。在网球中,GCN主要是指天线的结构、翅膀结构、远程通信和对的形成方式。蟋蟀独特的形态和行为特征,特别是与它们的配对方式和交配行为有关的特征,使它们成为了解昆虫进化和系统发育的关键群体。
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