黑斑侧褶蛙的两性异形和雌性繁殖特征

测定了黑斑侧褶蛙成体的体长、体重、头长、头宽、眼径、鼓膜径、前肢长、后肢长等形态指标以及雌体的怀卵数量。黑斑侧褶蛙雌体的体长和体重显著大于雄体。其它局部形态特征指标与体长呈正相关,协方差分析表明,雄体的鼓膜径大于雌体,其余形态指标不存在明显的两性差异。黑斑侧褶蛙雌体怀卵数量与体长和体重皆成正相关关系,表明黑斑侧褶蛙通过增加个体大小增加繁殖输出。     

泽陆蛙(Fejervarya limnocharis)两性异形的个体发育和雌体繁殖

2010年3月下旬-7月上旬于浙江富阳市农田采集680只泽陆蛙(Fejervarya limnocharis),研究了泽陆蛙成体和幼体的个体大小和局部形态特征的两性异形;通过解剖雌体获得窝卵数、测量抱对个体获得形态数据,研究了雌体大小与生育力关系以及抱对两性个体体形大小的相关性.结果表明:捕获个体中,雌性和雄性成体的最小体长分别为33mm和30 mm;雄性成体个体数显著超过雌性成体,两性幼体个体数无显著差异;两性成体头部大小、四肢长随体长呈同速增长,眼径和体重随体长呈异速增长,两性幼体所有被检形态特征均随体长呈同速增长;雌性成体平均体长显著大干雄性成体,去除体长差异的影响后发现,除眼径无显著的两性差异外,其余被检形态特征均为雌性大于雄性;幼体除雌性体重大于雄性外,其余被检形态特征均无两性差异;窝卵数与雌体大小(体长和体重)呈显著的正相关;两性抱对个体的体长无显著相关性;泽陆蛙雄性成体体形小于雌性成体的个体大小两性异形模式可能决定于驱使雄性向较大体形发展的进化驱动力相对较弱,雌性增大体形可增加繁殖输出,故向较大体形发展的进化驱动力相对较强;除体重外,其余被检形态特征的两性异形均形成于性成熟之后.     

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。     

密点麻蜥的两性异形和雌性繁殖

蜥蜴繁殖成功率与其形态特征有密切的关系。作者在内蒙古乌拉特后旗采集密点麻蜥(Eremias multio-cellata) ,定量研究该种形态特征的两性异形和雌体繁殖特征,检验与成体形态特征相关的两性繁殖成功率差异是否能促进两性异形的进化。密点麻蜥成体个体大小无显著的两性差异,但头部大小两性差异显著;雄性个体的头长和头宽均大于体长相同的雌性成体。繁殖雌体于五、六月份排卵;在实验室条件下,雌体在六月下旬至七月下旬之间产仔。该种雌体年产单窝仔,每窝2 -4仔。窝仔重与雌体体长呈正相关,但雌体体长仅能解释很少一部分(约19 %)窝仔重的变异。窝仔数和幼仔重均与雌体体长无关。幼仔重与相对生育力(相对于雌体体长的窝仔数)呈显著的负相关,表明该种蜥蜴存在后代数量-大小之间的权衡。密点麻蜥雄体和雌体向较大体型方向进化的选择压力均相对较弱,与成体头部大小相关的两性繁殖成功率的差异是导致该种蜥蜴头部大小两性异形进化的主要原因[动物学报52 (2) : 250 -255 , 2006]。     

雌性凹耳蛙生育力与体型参数间相关性及其配对模式

为了探究雌性凹耳蛙(Odorrana tormota)生育力与体型参数之间是否存在相关性,测量了黄山浮溪地区23只排卵后雌蛙的体重、体长、头长、头宽、前臂宽、前肢及指长、前肢长、后肢全长、胫长等9个体型参数,并计数每只雌蛙的窝卵数。相关性分析显示,雌蛙的窝卵数和9个体型参数值均呈正相关性(P 0.05),体长和其他8个体型参数值均呈现正相关性(P 0.05),以体长为控制变量,偏相关分析显示,窝卵数和体重呈正相关性(P 0.05),故具有较长的体长、较重的体重特征的雌蛙,可以携带更多的卵,具有更强的生育能力。不同雌蛙个体间的窝卵数差异较大,平均窝卵数为(646.5±37.6)枚(590～706枚)。大个体雌蛙具有更强的生育力、更大的繁殖输出,可能是导致凹耳蛙两性间异形程度较大(雌大雄小)的重要驱动力。为了探究抱对雌、雄凹耳蛙之间的配对模式,测量了21对抱对雌、雄蛙的上述9个体型参数,分析显示,抱对雌、雄间9个体型参数值均不存在相关性(P 0.05),未发现凹耳蛙在性选择的过程中采用选型配对模式,雌性凹耳蛙可能倾向雄蛙非体型的品质特征,比如鸣叫声等。     

多疣狭口蛙昆明种群雌雄配对行为及形态适应选择

测量和比较采自昆明东北郊的24对抱对多疣狭口蛙(Kaloulaverrucosa)标本,同时野外观察其繁殖行为。配对雌雄蛙的体长、体重和头宽3个形态特征的Pearson相关系数大于0·5;择体长和体重作回归分析,结果表明,雌雄蛙体长选择和雌雄蛙体重配对都呈良好的线性关系。雌蛙选择雄蛙体长为自身体长的(81·8±5·7)%、体重为自身体重的(53·1±10·7)%的个体为最适配偶。雌蛙选择体长较长而体重较轻的雄蛙作为配偶,这样有利于形成较好的空间(雄性胸腹部皮肤腺长度,雌雄抱对时泄殖孔位置等)配对关系。多疣狭口蛙属于雌性选择模式,即雄蛙鸣叫,雌蛙受吸引,主动接近雄蛙,如果雄蛙条件适合则形成配对。     

斯洛维尼亚池塘中大蟾蜍的交配模式

为了解大蟾蜍( Bufo bufo)的配对成功是否与身体大小有关,在蟾蜍产卵之前,我们在斯洛文尼亚捕捉和测量了2 224只成体样本。在这些捕获的个体中, 1 772只为雄性, 452只为雌性,其中355对处于抱对状态。雌性的体长(从吻端到泄殖腔的距离)一般比雄性稍长。无论雄性还是雌性,抱对者的体长均大于未抱对者。抱对的雄性和雌性的体长具有显著的正相关。我们所发现的大小匹配的交配模式,与从其它普通蟾蜍种群得到的结果一致[动物学报51 (3) : 513 -515 , 2005]。     

多疣狭口蛙昆明种群雌雄配对行为及形态适应选择

测量和比较采自昆明东北郊的24对抱对多疣狭口蛙(Kaloula verrucosa)标本，同时野外观察其繁殖行为。配对雌雄蛙的体长、体重和头宽3个形态特征的Pearson相关系数大于0.5；择体长和体重作回归分析，结果表明，雌雄蛙体长选择和雌雄蛙体重配对都呈良好的线性关系。雌蛙选择雄蛙体长为自身体长的(81.8±5.7)%、体重为自身体重的(53.1±10.7)%的个体为最适配偶。雌蛙选择体长较长而体重较轻的雄蛙作为配偶，这样有利于形成较好的空间(雄性胸腹部皮肤腺长度，雌雄抱对时泄殖孔位置等)配对关系。多疣狭口蛙属于雌性选择模式，即雄蛙鸣叫，雌蛙受吸引，主动接近雄蛙，如果雄蛙条件适合则形成配对。     

蓝尾石龙子的生长、两性异形及雌性繁殖

报道蓝尾石龙子（Eumeces elegans)的生长、两性异形和雌性繁殖,性成熟个体体色的两性差异显著,成年雄性体长、头长和头宽显著大于成年雌性,幼体体长生长率无显著的两性差异。成年雄体体长生长率显著大于成年雌体,因此,个体大小的两性异形是性成熟后发生的,体长小于50mm的幼体,头长和头宽无性差异;当体长大于50mm。雄性头长和头宽随体长的生长率显著大于雌性。并导致头部大小的两性异形,并随个体发育变得越来越显著,蓝尾石龙子产卵雌体的最小体长为69.3mm,大于此体长的雌体均年产单窝卵。窝卵数、窝卵重和平均卵重均与雌体体长呈正相关,平均值分别为6.4、2.783和0.554g。窝卵数与雌体产后状态无关,蓝尾石龙子雌体主要通过增加窝卵数和卵大小来增加繁殖输出。     

近距离交流信号对雌性凹耳蛙 抱对成功率的影响

繁殖期雌性凹耳蛙（Odorrana tormota）的声信号已有过深入的研究,但目前国内对其交配行为研究较少,近距离时,雌性凹耳蛙如何与雄蛙交流并完成抱对尚不清楚。为探究繁殖期雌性凹耳蛙与雄蛙近距离交流、交配过程,采用焦点动物取样法和全事件取样法对雌性凹耳蛙交配前行为进行记录。2013至2016年及2018年记录并分析了49组雌雄蛙抱对过程和42组未抱对个体的视频数据。结果表明,凹耳蛙雌蛙与雄蛙近距离交流过程涉及多种信号,包括视觉信号（眨眼、低头、腹部膨胀、脚趾震动、背转向雄蛙）与声信号两类;在每组雌蛙发出信号且抱对成功的实验中,各视觉信号出现1或2次较多,声信号出现1至3次较多,眨眼、鸣声、腹部膨胀三种信号的总次数较多;5个繁殖期所记录的雌蛙交流信号中视觉信号所占的比例均高于声信号。统计分析结果显示,同一只雌蛙在抱对成功与失败时所发出的眨眼、低头和腹部膨胀三种视觉信号的次数存在显著性差异（P < 0.05）,声信号、腹部膨胀、脚趾震动和背转向雄蛙这四种信号仅在抱对成功时出现。因此,推测这些信号在抱对前出现时,有助于提高雌雄凹耳蛙抱对成功率。     

Effects of parental body condition and size on reproductive success in a tenebrionid beetle with biparental care

Abstract. 1. The beetle Parastizopus armaticeps (Coleoptera: Tenebrionidae) inhabits the Kalahari desert of southern Africa, constructs breeding burrows after rainfall, and shows extensive biparental care. Previous work has shown that it is predominantly male size, not female size, that determines breeding success; however, in the field these beetles show size assortative mating. This might obscure or override effects of female size on reproduction. Moreover, the inaccessibility of the breeding burrows makes it impossible to test effects of female and male size on offspring development and survival before adulthood. 2. To disentangle the effects of male and female length, body mass, and body condition on reproductive success, males and females were paired randomly in small breeding cages in the laboratory (n = 887 breeding pairs). The construction of the breeding cages allowed a clear view of the brood chamber contents at each stage in offspring development. Larva, pupa, and imago numbers and development were monitored daily, and imago mass at hatching from the pupa (hatchlings), offspring mass, and offspring body length at complete exoskeleton melanisation (juveniles) were determined. 3. There was a weak positive correlation between body condition and body length for females only. Breeding chronology was related to male body condition: males in better condition were fast to start and finish a breeding bout. Males in better condition produced heavier hatchlings and juveniles, and larger‐sized males produced larger‐sized juveniles. In contrast, numbers of larvae and juveniles produced were determined mainly by female length and body condition: larger females in better condition hatched more larvae and produced more offspring. 4. The results suggest that male size and condition will be the most important determinant of reproductive success under relatively dry conditions, when burrow length is critical for reproductive success. Female size might be more important for the pair's reproductive success under wet breeding conditions, when burrow length is less critical for successful reproduction.     

Male mate choice in the chameleon grasshopper (Kosciuscola tristis)

In many species, males can increase their fitness by mating with the highest quality females. Female quality can be indicated by cues, such as body size, age and mating status. In the alpine grasshopper Kosciuscola tristis, males can be found riding on subadult females early in the season, and as the season progresses, males engage in fights over ovipositing females. These observations suggest that males may be competing for females that are either unmated (early season) or sperm‐depleted (late season). We thus hypothesised that male K. tristis may be choosy in relation to female mating status, and specifically, we predicted that males prefer females that are unmated. We conducted behavioural experiments in which males were given the choice of two females, one mated and one unmated. Contrary to our prediction, males did not mate preferentially with unmated females. However, copulation duration with unmated females was, on average, 24 times the length of copulation with mated females. While female K. tristis can reject mates, we did not observe any evidence of overt female choice during our trials. Females may gain additional benefits from mating multiply and may therefore not readily reject males. While our experiment cannot definitively disentangle female from male control over copulation duration, we suggest that males choose to invest more time in copula with unmated females, perhaps for paternity assurance, and that male mate assessment occurs during copulation rather than beforehand.     

Laboratory breeding studies of freshwater crayfish, Austropotamobius pallipes (Lereboullet)

SUMMARY. 1. Mature crayfish, collected from an Irish lake before breeding had started, were held in breeding combinations and their mating and brooding activities observed.
2. All mating attempts were initiated by the male. A single mating led to spawning within 6 days but a subsequent mating cancelled the effects of the first. Males mated more often when there were more females present. Males lacking a major cheliped mated less often than did normal males.
3. Larger males mated more often than did smaller males, and although males showed no female size preference, matings were less frequent and generally unsuccessful when males were much larger than females; the female was usually killed. Large females mated successfully with smaller males.
4. Females held at high densities with a larger male mated earlier than at low densities. However, aggression also increased with density; at high densities males fought and killed females.
5. Males held in pairs without females fought; in occasional mating attempts spermatophores were not positioned correctly. Paired females rarely fought; all spawned normally although unmated. Although their eggs soon died and were removed during grooming, brooding behaviour continued for at least 2 months.
6. Brooding females held in pairs shed pleopodal eggs during aggressive encounters. Females held singly showed a lower initial rate of egg loss.     

Mate Switching in a Non-monogamous Species? The Case of the Common Quail (Coturnix coturnix)

We investigated the occutrence of mate switching in the common quail, a non-monogamous species with a temporal pair bond but without either male parental care or territoriality. The study was carried out throughout the breeding seasons of 1993–95 in Mas Esplugues (Catalonia, Spain) by monitoring 28 radio-tagged couples and 17 radio-tagged unpaired males. Agonistic interactions between males inside funnel traps containing a female were also recorded. Mate switching within the laying period occurred in 72% of the females, and new partners always had a higher body condition index than old partners. Agonistic interactions inside the funnel traps also showed that successful males had a better body condition index than losers. These results, along with the observed mate-guarding behaviour of females by their partners throughout the laying period, a highly male-biased sex ratio (five males per female), the lack of territoriality of males and the expected difficulties which unmated males experience in finding pairs, suggest that mate switching is not induced by paired males. Moreover, the constant inflow of new males observed throughout the fertile period of the female and the low costs stemming from mate change strongly support the idea that it is paired females who induce mate switching, in order to improve their fitness by mating with the best quality male available at every moment of their fertile period.     

Female pied flycatchers trade between male quality and mating status in mate choice

According to mate choice theory, females should consider both male quality and mating status when choosing a mate. In birds, strong experimental evidence indicates that females prefer males with elaborate traits. No comparable evidence exists to determine whether females take male mating status into account or how they may trade between male quality and male mating status. We studied mate choice of female pied flycatchers (Ficedula hypoleuca) in outdoor aviaries where the effect of territory quality could be eliminated and where we could control which males were mated and which were unmated. We used male plumage colour as our measure of male quality. In the aviaries, focal females could easily compare males and assess their plumage colour and mating status, and resident females were prevented from attacking prospecting females because of separation in different compartments. The study provided evidence for a trade-off in mate choice. Females may compromise by choosing an already mated male if he is more brightly coloured and, presumably, of higher quality than available unmated males. The study did not support the idea that polygyny is based on male deception of females, but the results were consistent with the female aggression hypothesis.     

Non-random mating by size in American toads, Bufo americanus

Male American toads, Bufo americanus, captured in amplexus at least once during the season were significantly longer than males captured only singly in the same breeding population in all three cases studied. Absence of any correlation between the body lengths of the members of amplexing pairs argues against selection for optimal relative size. Males successful at breeding were those that (1) were larger, (2) were at the pond more nights, and (3) spent more time calling than unsuccessful males. Residency, per se, did not enhance breeding success, however, as on any given day successful males were equally likely to come from recaptured males previously present at the pond and unmarked males presumed new to the pond. Amount of movement about the pond did not vary with breeding success; all males tended to remain in one area on any given night and to change areas between nights. A very low displacement rate (about 7%) of males in amplexus argues against primacy of this form of male-male competition in producing differential mating by size. Rather it appears that some combination of other forms of intrasexual competition and female choice caused the mating pattern seen.     

A biomechanical perspective on the use of forelimb length as a measure of sexual selection in frogs

Differences in forelimb length between male and female frogs and between amplexing and non-amplexing males have been interpreted to be the results of sexual selection on forelimb length. The causal feature of the forelimb that has been posited to cause such selection is the observation that non-amplexing males attempt to disrupt breeding by prying amplexing males from females. A biomechanical model of forelimb function suggests that total length per se may not be the most appropriate measure to use. There are more functionally significant aspects of forelimb morphology, such as lever arm lengths, that should influence amplexing ability and may make measures of overall forelimb length misleading. This example highlights the relevance of functional analysis to current questions in evolutionary biology that rely on postulated roles for morphological structures under selection.     

Female choice of large males in the treefrog Hyla ebraccata

The mating behaviour and male mating success of Hyla ebraccata were examined over three study periods. Mated males were larger than unmated males on a significant number of nights and for one of the three study periods. In field observations of pair formation, female behaviour was consistent with choice of large males: females moved freely through the chorus, remaining within 10 cm of males larger than the nightly mean, before the male initiated amplexus. In 27% (n = 3) of these observations, males chased and fought over the female. However, the females removed two of these three males from amplexus, suggesting that females can also exercise choice after amplexus. There was a significant negative correlation between male size and dominant frequency of the primary note, indicating that the male's advertisement call contained size-related information. Comparisons of the size of mated and unmated males suggest that two factors may have affected the degree to which female choice influenced male mating success. First, the distance between calling males may have limited the opportunity for females to express a mating preference. Secondly, an increase in mean and a decrease in the variance of male size in one of the three study periods also may have limited the ability of females to express a preference for large males.     

Assortative Mating by Size in the American Rubyspot Damselfly (<Emphasis Type="Italic">Hetaerina americana</Emphasis>)

Assortative mating refers to the non-random nature of mating patterns between certain males and females. Thus, males and females may associate negative- or positively, based on different traits. Amongst these associations, assortative mating by size is one of the most common patterns found in natural populations of animals. Two main hypotheses have been proposed to account for the occurrence of assortative mating by size. First, it may be the result of mechanical, temporal, or physiological constraints. Second, it may occur in response to direct or indirect selection on mating preferences. Here we investigate whether the American rubyspot damselfly exhibits true assortative mating by size. Males of this species exhibit high levels of male-male competition, as they compete over territories, to which females are attracted for copulation. There is a documented large male body size advantage: the largest males are better able to hold their territories and thus secure more copulations. Our major results show that i) mated males are more likely to be larger than unmated males, whereas mated and unmated females tend to have similar body sizes; ii) H. americana exhibits true assortative mating by size; as such, this pattern is not driven by seasonal changes in the body sizes of males and females. We suggest that this mating pattern occurs in this species given the advantages of large male size, and the advantages of large female body size (i.e. higher fecundity). We believe that males may be able to evaluate a female’s reproductive value and exert mate choice.     

Factors influencing male mating behaviour in Gambusia affinis (Baird & Girard) with a coercive mating system

The effects of male and female body size, and correlated characteristics, on male mating behaviour were investigated in the western mosquitofish Gambusia affinis . Because larger females typically have larger broods in Gambusia sp., it was predicted that males would attempt more copulations with larger females. Two-way ANOVA showed that female body size was a significant predictor of male mating behaviour but male size was not. The effects of a suite of additional traits (both male and female) on male mating attempts were also tested. In a stepwise multiple regression, female standard length ( L _S), size of the female gravid spot and male testes mass were significant predictors of male mating attempts, accounting for c. 27% of variation in male mating. Path analysis showed that differences between male and female L _S, male body condition and male testes mass were significant predictors of male mating attempts, and also accounted for 27% of the variation in male mating attempts. The two statistical models were very similar in their predictive power, but differed slightly in significant predictor variables. Results confirm that factors other than female size are important predictors of male mating behaviour in the western mosquitofish.