蜜蜂的交配行为

蜜蜂是一妻多夫制，处女蜂王可与７－１７只雄蜂交配。说细介绍了雄蜂内阳茎的构造，交配时内阳茎翻出体外的过程，蜂王和雄蜂交配的情况，一次交配后留在蜂王蜇针腔的交配标志，以后与蜂王交配的雄蜂如何将堵塞在蜇针腔的交配标志除去的过程。     

饲养条件下东北虎交配行为的观察

1999年和 2 0 0 0年的 1 1～ 1 2月期间共记录了黑龙江东北虎林园 1 6对东北虎的 1 693次交配事件 ,对其中 1 1 92次成功的交配事件进行了分析 ,建立了东北虎的交配行为谱 ,记录了 1 6种个体行为和 7种社会行为。东北虎的交配持续期为 (6 5 0± 2 5 0 )d ,不同繁殖对的交配次数差异很大 ,最少为 49次 ,最多可达 1 1 3次 ,交配成功率为 70 41 %。东北虎的交配高峰出现在 8∶0 0～ 1 0∶0 0时和 1 6∶0 0～ 1 8∶0 0时。交配成功的次数在第 3～ 5d达到高峰 ,失败的次数在开始交配时最高 ,以后则逐渐降低。在将雌、雄虎赶入小围栏内的首次爬跨前东北虎需花费 (2 0 2 4± 1 2 85 )min的时间做准备 ,其后的各次爬跨与首次相似 ,只是花费时间大大缩短 ,且持续的时间相差很大 ,最短仅为 4 70s,最长则达 6 3 1min。交配后的休息过程同时也是下一次交配前的准备阶段。每次将雌、雄虎赶入小围栏内东北虎要连续进行 (9 40± 4 60 )次爬跨 ,整个交配过程持续 (1 2 67± 3 0 5 )min ,每次爬跨历时 (1 0 0 9± 5 45 )s。     

黑龙江省圈养狼交配行为的初步观察

2005 年10 月至2006 年4 月,采用焦点动物取样法和全事件扫描取样法,对黑龙江省哈尔滨北方森林动园4 对圈养狼交配活动进行了观察,以期了解无人干扰下圈养狼的交配过程及其交配模式。观察时间共计25 d, 225 h,实际录像时间为126 h,记录到爬跨741 次,成功交配46 次,成功爬跨交配占总爬跨次数的6. 2% 。狼在交配过程中有锁结现象,雄狼通常在一次爬跨、多次抽动后出现射精。交配行为一般发生在8∶ 00 ～10∶ 00和14∶00 ～ 16∶ 00。雌性具有明显的邀配模式,一旦邀配成功,雌狼站立不动,尾巴偏向一侧,腰部微下躬,配合雄狼爬跨。对交配参数进行单因素方差分析,4 只雄狼的抽插时间没有差异(P = 0. 827),而其锁结行为的时间差异极其显著(F = 71.43,P <0.001),交配期持续5 ～ 14 d,交配平均持续时间为534 ± 402 s,最长达1 588 s,
最短只有28 s。     

甜菜夜蛾交配行为和能力

在(27±1)℃,光周期L14∶D10的条件下对甜菜夜蛾I>Spodoptera exigua的交配行为及能力进行了研究。结果表明：成虫在羽化当晚即可进行交配,交配率以羽化后头三个晚上的较高(>82%),但从第4天起则显著下降。成虫一天中的交配时间出现于23:30～05:30之间,交配高峰出现在01:30～02:30和03:00～04:00 之间, 其中以第1高峰的发生频率较高。成虫交配持续时间从22～191 min不等,但以30～60 min的为多(40.8%, n=97), 60～90 min的次之(19.4%),超过180 min的较少(10.2 %)。另外,交配持续时间与蛾龄紧密相关。蛾龄越大,交配持续的时间越长,且差异显著。雄蛾一生的交配能力由1～11次不等,但受性比的影响显著：在性比为1∶1的条件下,雄蛾平均交配次数仅为3.0 次,而在2♀∶1♂至5♀∶1♂时,则增加到5.1～6.0 次。雌蛾交配比例及次数受性比的影响也很大：没有交配的雌蛾比例从1∶1时的8.3%增加到5♀∶1♂时的32%,仅交配一次的比例从16.7%增加到38.7%,而交配≥5 次的比例则从 25%下降到0。最后,对这些结果在甜菜夜蛾防治中应用的可能性进行了讨论。     

大猿叶虫交配行为的观察

大猿叶虫Colaphellus bowringi Baly是十字花科上的重要害虫,一生能多次交配。本试验在25℃,光周期L∶D=12∶12条件下观察了大猿叶虫成虫连续7d的交配行为。结果表明:(1)每日平均交配(5.67±0.26)次,最高可达11次,不同日龄间的交配次数存在显著差异。(2)平均每日用于交配的时间为(238±10)min,占总时间的33.5%,最长可达493min,占总时间的68.5%,不同日龄间的交配时间有极显著差异。(3)交配持续时间最短8min,最长达289min,平均为(48±2)min;同一日内,随着交配次数增加,交配持续时间逐渐缩短;不同日龄间的交配持续时间存在显著差异。(4)相邻两次交配之间的间隔时间最短5min,最长300min,平均交配间隔(75±3)min;交配间隔时间随日龄的增加而明显延长。     

圈养条件下金钱豹交配行为的初步观察

2005年3月至2006年3月,采取所有事件取样法,对成都动物园5只(2雄,3雌)圈养金钱豹(Panthera pardu)进行观察,旨在了解圈养金钱豹的交配情况。记录交配行为1 174次。结果显示,圈养金钱豹全年皆可发情。具有明显的交配模式,交配姿势仅有一种,为背腹式。平均交配持续天数为(4.75±1.26)d。昼夜都有交配行为,但白天交配次数较夜间多。日交配的高峰发生在08:00～10:00时,不同的雄性个体出现的交配高峰日不同。平均交配持续时间为(7.48±1.22)s。在交配持续时间(P=0.000)、总交配次数(P=0.04)上,不同的雄性个体间存在显著性差异;而同一雄性在与不同雌性交配时,其持续时间无显著差异。金钱豹交配的特点为,交配的频次多,但每次交配持续时间短。     

半散养状态下东北虎交配行为的观察

在2006～2007年,采用行为取样法对泰山东北虎园7只(3雌,4雄)半散养状态下(园区占地面积20 000 m2)的东北虎的交配活动进行了为期22 d的观察,旨在了解无人干扰下东北虎的交配过程及其交配模式.结果显示:东北虎在交配过程中无锁结现象,雄虎通常在一次爬跨多次抽动后即出现射精.在1 h内出现2次射精次数的比例占总射精次数的74.0%.东北虎的交配模式属于Dewsbury分类系统中的第11种,即无锁结、有抽动、单次插入、多次射精.交配期内,每只雌虎平均日邀配28±3次,平均邀配持续时间为20.0±1.2 s;每只雄虎平均日爬跨14±1次.平均抽动持续时间为20.9±0.5 s,平均交配持续时间为45.2±1.3 s.     

北草蜥的交配行为

在围栏条件下,观测北草蜥(Takydromus septentrionalis)的交配过程,分析其行为模式,旨在建立北草蜥交配行为谱,探讨雄性交配成功率与个体特征的关系。北草蜥交配行为的一般模式为:雌雄接近→咬尾→咬腹→交媾。该行为过程的持续时间分别为0.53m、1.77m、0.47m和141.3m。所观察到的51对成功交配中,70%的配对为雄体>雌体,且雄体平均体长和体重显著大于配对雌体。雄体的交配成功率与其体长成正相关,但与头长、头宽、尾长、体重及体色均无显著相关性。     

水稻二化螟的交配行为

在室内条件下,对水稻二化螟Chilo suppressalis的交配行为及能力进行了研究.结果表明：大多数二化螟雌蛾一生只交配一次,平均0.92次;而雄蛾具有多次交配能力,最多达4次,平均2.72次.二化螟雌蛾的日龄影响其交配率、交配起始时间和持续时间,随二化螟雌蛾日龄的增加,其交配率逐渐下降,交配起始时间逐渐提前,而交配持续时间逐渐上升.相反,二化螟雄蛾日龄对其交配率、交配起始时间和持续时间没有明显影响.交配日龄对二化螟雌蛾的生殖力也存在显著影响,随着二化螟雌蛾交配日龄的增加,雌蛾产卵量下降,卵孵化率降低,产卵期缩短,它们都与雌蛾交配日龄存在显著的负相关;而雌蛾产卵前期和雌蛾寿命随雌蛾交配日龄的增加而延长,与雌蛾交配日龄存在显著的正相关.但二化螟雄蛾交配日龄对雌蛾的生殖力没有明显影响,二化螟雄蛾一生都具有较强的交配繁殖能力.同时,不同交配史的雄蛾与雌蛾交配,对雌蛾的生殖力也没有显著影响.表明二化螟的交配活动是由雌蛾主导控制的.最后,对这些结果在二化螟性信息素防治中应用的可行性进行了探讨.在应用性信息素控制二化螟的实践中,可以在两方面取得实效,一是性信息素可以阻碍雌雄之间正常交配,降低交配率;二是可以推迟二化螟雌虫的交配,使其产卵量和卵孵化率降低.     

亚洲象的求偶交配行为观察

本文试用多样性指数公式对亚洲象的求偶交配进行分析,结果雄象的Ｈ值较高,表明雄象的求偶交配行为多样且容易发生。     

Mate discrimination in Littorina littorea (L.) and L. saxatilis (Olivi) (Mollusca:Prosobranchia)

The ability of males of Littorina littorea and L. saxatilis to discriminate between mates of different sex, species and size was examined. In partner choice experiments males of L. littorea had the possibility to initiate a copulation with either a female or a male. The males did not show a preference for either sex. There was therefore no evidence that they could determine the sex of a conspecific prior to copulation. The duration of intrasexual copulation was considerably shorter than for intersexual copulation, both in the field and in laboratory experiments. For the two species, intersexual copulations were far more frequent than intrasexual ones. This can partly be explained by the difference in copulation time.Few interspecific copulating pairs were found on the shore. This may reflect a low interspecific encounter rate rather than a mechanism of species recognition. On all of these occasions, however, the active male was of L. saxatilis. It is argued that selection against precopulatory species and sex recognition is a more likely explanation than an hypothesis that states that the required mutations for precopulatory mate identification has not yet occurred. L. littorea males copulated longer with large than with small females. Copulation time was short with parasitized females, which are sterile or of low fecundity. The allocation of mating effort by males is discussed.     

Effects of reproductive state and host resource experience on mating decisions in a walnut fly

Prior experience with conspecifics or essential resources, aswell as physiological condition, can have important influenceson an animal's reproductive behavior. While effects of experienceand physiological state (such as reproductive condition) aregenerally treated separately in theoretical discussions, theyoften interact. No previous study has attempted to distinguisheffects of experience on physiological state from other effectsof experience in the context of mating behavior. In a studyof a walnut-infesting tephritid fly (Rhagoletis juglandis),we examined the effects of host fruit experience on mating behavior.We manipulated physiological state in terms of egg load (definedas the number of mature oocytes in a female's ovaries) independentlyof fruit experience to distinguish the effects of these variables.We found that females with high egg loads were significantlymore likely to copulate than low–egg load females; thelevel of fruit experience had no effect on propensity to copulate,except via effects on egg load. In contrast, females with priorexposure to fruit copulated for a significantly shorter durationthan control females, while egg load had no effect on copulationduration. These results suggest that female reproductive conditionand exposure to essential resources can have important, albeitdiverse effects on mating behavior. We discuss how distinguishingdifferent types of variables may provide insight into sexualconflict over mating decisions, as well as which sex controlsspecific aspects of behavior.     

The effect of female mating history on sperm precedence in the two-spot ladybird, Adalia bipunctata (Coleoptera, Coccinellidae)

Effects of two different mating regimes on sperm precedencein the two-spot ladybird, Adalia bipunctata, were studied usingthe polymorphic gene for melanism as a marker for paternity.Virgin nonmelanic females (homozygous recessive) were matedto nonmelanic male(s) and then, after laying fertilized eggs,were mated to a melanic male of known genotype. The resultsafter the two successive single matings showed a highly variabledegree of paternity of the second male. Initial multiple matingwith nonmelanic males did not alter the pattern of paternityafter the subsequent single mating with a melanic male, butit had two other effects: (1) the female showed an increasein rejection behavior, and (2) a longer copulation was requiredfor high success of the melanic male. Additional observationsin which families were reared from beetles collected in copulain the field demonstrated that sperm competition also occursunder natural conditions. The outcome of the competition wasvariable with frequent sperm mixing.