鲶鱼和胡子鲶的两性异形与雌性个体生育力

检测了鲶鱼(Silurus asotus)和胡子鲶(Clarias fuscus)繁殖期18个形态特征的两性异形以及雌性个体生育力。结果表明,鲶鱼和胡子鲶雌雄性别比例均符合1∶1。One-way ANOVA显示,鲶鱼雌雄个体体长差异不显著,胡子鲶雌性个体体长显著小于雄性个体(P0.05)。以体长为协变量的One-way ANCOVA显示,特定体长的鲶鱼雌性个体的眼间距和体高显著大于雄性个体(P0.05),两性间其它局部特征不存在显著的两性差异;特定体长的胡子鲶雌性个体的体高、腹鳍基前距和腹鳍臀鳍间距显著大于雄性个体,雌性个体的臀鳍基长、尾柄高和尾鳍长显著小于雄性个体(P0.05),两性间其它局部特征不存在显著的两性差异。Two-way ANOVA显示,胡子鲶体长显著大于鲶鱼(P0.05),性别及物种与性别两因素的相互作用对体长影响不显著。以体长为协变量的Two-way ANCOVA显示,胡子鲶的头长、头宽、吻长、眼间距、尾柄高、尾鳍长、背鳍基前距、背鳍基长、腹鳍基前距、腹鳍臀鳍间距、体重和去内脏体重显著大于鲶鱼,头高、体高、臀鳍基长显著小于鲶鱼(P0.05),物种间的其他形态特征变量差异不显著;雌性个体的体高、背鳍基前距、腹鳍基前距、腹鳍臀鳍间距显著大于雄性个体,臀鳍基长、尾柄高、尾鳍长、背鳍基长显著小于雄性个体(P0.05),两性间的其他形态特征变量差异不显著;物种与性别两因素的相互作用对体高、臀鳍基长、尾柄高、尾鳍长、背鳍基长和腹鳍臀鳍间距影响显著,对其余的形态特征变量影响不显著。15个形态特征变量的主成分分析(Eigenvalue≥1)发现,前2个主成分共解释68.4%的变异。头宽、眼间距、尾柄高、尾鳍长、背鳍基前距、背鳍基长、腹鳍基前距和腹鳍臀鳍间距在第一主成分有较高的正负载系数,臀鳍基长在第一主成分有较高的负负载系数(解释51.2%变异);眼后头长在第二主成分有较高的负负载系数(解释17.2%变异)。胡子鲶在第一主成分和第二主成分的分值均显著大于鲶鱼,雌雄两性的差异以及两因素的相互作用对分值的影响均不显著。实验检测的鲶鱼、胡子鲶的怀卵数量与体长和体重回归关系显著。One-way ANCOVA及矫正平均值Tukey's检验显示,特定体长的胡子鲶的产卵数量显著大于鲶鱼。性选择是胡子鲶大个体雄性形成的主要原因,同时影响与运动相关的尾部特征。生育力选择更多的影响与雌性胡子鲶较大腹腔容积相关的形态特征变异。环境因子、食物可得性和营养状况同时影响了个体大小两性异形的形成。     

鳄蜥的两性异形

通过比较鳄蜥的体型与头部大小等特征的差异,研究了鳄蜥的两性异形情况.结果表明:性成熟鳄蜥个体体色差异显著,成年雄性头胸部腹面呈鲜红色或浅蓝色,而雌性为浅黄色或淡红色;成年雄性头部显著大于成年雌性(头长(HL),P＜0.001;头宽(HW),P＜0.001),成年雌性腹部长(AL)显著大干成年雄性(P=0.018);而成...     

四眼斑水龟个体大小和体形的两性异形

研究龟鳖的两性异形对理解形态适应具有重要意义。通过测量41只(21♀,20♂)成体四眼斑水龟(Sacalia quadriocellata)的20个形态特征指标,研究四眼斑水龟个体大小和体形的两性异形。结果表明:除头长、头宽、尾长和尾长肛前段长外,四眼斑水龟其他的形态特征均与背甲长呈正相关。雌性的背甲长、腹甲长、腹甲中线长、腹甲曲线长显著大于雄性;雄性的头长、头宽、后肢长、尾长和尾长肛前段长显著大于雌性;雌雄两性的体重、体周长、前肢长、腹甲宽、肛盾切口长、肛盾切口宽以及除背甲长外的所有背甲形态特征指标均无显著差异。研究结果表明,四眼斑水龟存在个体大小和体形两性异形。     

乐山棒花鱼形态特征的两性异形和雌性个体生育力

测定了乐山棒花鱼(Abbottina kiatingensis)繁殖期形态特征包括体长、头长、头宽、头高、吻长、眼后头长、眼径、眼间距、体高、尾柄长、尾柄高、尾鳍长、背鳍基前距、背鳍基长、腹鳍基前距、腹臀间距、体重和去内脏体重的两性异形和雌性个体生育力。繁殖期雄性个体的数量显著多于雌性个体,雌雄两性个体的体长差异不显著。特定体长的雌性个体的头长、头宽、头高、吻长、眼后头长、尾柄高、背鳍基前距、背鳍基长和去内脏体重显著小于雄性个体,其余指标不存在明显的差异。回归分析表明,乐山棒花鱼的怀卵数量与体长和体重回归关系显著,雌性通过个体大小(体长和体重)的增加来提高个体生育力。     

棒花鱼形态特征的两性异形和雌性个体生育力

测定了棒花鱼(Abbottina rivularis)繁殖期形态特征包括体长、头长、头宽、头高、眼间距、鼻间距、背鳍基长、胸鳍长、胸鳍腹鳍间距、尾柄长、尾鳍长和体重的两性异形和雌性个体生育力。结果表明,雄性个体的数量显著多于雌性个体,雄性个体的体长显著大于雌性个体。特定体长的雌性个体的胸鳍腹鳍间距显著大于雄性个体,头长、头宽、头高、眼间距、鼻间距、背鳍基长、胸鳍长、尾柄长和尾鳍长显著小于雄性个体,雌雄两性体重不存在显著差异。棒花鱼的怀卵数量与体长和体重回归关系显著。偏相关分析显示,当控制第三者恒定时,怀卵数量与体长和体重呈正相关但不显著。棒花鱼存在个体大小和其他局部特征显著的两性异形,雌性个体主要通过腹腔容积的增加提高个体生育力。棒花鱼形态特征的两性异形是性选择和生育力选择共同作用的结果。     

黄颡鱼的两性异形和雌性繁殖特征

测定了黄颡鱼成体的体长、头长、头宽、头高、吻长、眼径、眼间距、眼后头长、体高、尾柄高、背鳍基前距、背鳍基长、尾柄长、腹鳍基前距、背鳍脂鳍间距、腹鳍臀鳍间距、尾鳍长、体重、去内脏体重等形态指标以及雌体的怀卵数量。雌性成体的体长显著小于雄性成体。其它局部特征皆与体长呈正相关,回归剩余值的t—检验表明,雌性成体的眼径、头高、体高、腹鳍基前距、体重显著大于雄性成体,其它局部形态特征不存在显著的两性差异。黄颡鱼雌体通过个体大小的增加和腹部形态的改变增加腹腔容量,增加繁殖输出。     

海陆蛙的两性异形和雌性繁殖特征

用采自海南东寨港红树林保护区的58只(35 ♀♀,23 ♂♂)成体海陆蛙(Fejervarya cancrivora),通过测量头体长、体重、头长、头宽、吻长等11个形态特征指标和雌体卵巢质量(窝卵重),研究该种形态特征的两性异形和雌性繁殖特征,并检验雌性成体大小(头体长和体重)与其繁殖的相关性.雌雄两性个体的最小头体长分别为44.9 mm和45.2 mm.除吻长和眼间距外,其余局部形态特征与头体长皆呈正相关性.头体长在雌雄两性之间差异显著,雌性显著大于雄性;而体重、头长、头宽等局部形态均无两性差异.海陆蛙雌体的窝卵重与头体长和体重之间皆成正相关关系,表明雌性可能是通过增大体型从而增加繁殖输出,而向较大体型发展.     

大蹼铃蟾的两性异形

2018年6—8月,测量采自云南省昆明市金殿水库后山的71只(47♂,24♀)大蹼铃蟾Bombina maxima成体的体长、头长、头宽等15项形态特征指标并检验该物种的两性异形。结果表明:雄性平均体长为53.54 mm±1.14 mm,雌性平均体长为52.74 mm±1.45 mm,雄性与雌性平均体长比为1.015,两性异性指数为0.01;大蹼铃蟾的体长、体质量与性别之间的差异无统计学意义;除了雌性的眼间距外,其余13项形态特征与体长均有极显著相关性;以体长为协变量的协方差分析结果显示,大蹼铃蟾的头长、吻长、前臂宽、腿或后肢全长、胫长、胫宽和跗足长在两性间的差异有高度统计学意义;雄性的这7项形态特征随体长的生长速率大于雌性。性选择假说能解释大蹼铃蟾的两性异形现象。     

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。     

斑腿泛树蛙两性异形和雌性繁殖能力及其影响因素

研究两栖类物种雌雄间的形态差异,不仅有助于理解物种两性异形的模式与机制,而且对其繁殖策略、繁殖投入和进化选择压力的研究都具有重要意义。2020年4月至2021年8月以浙江省丽水市丽水学院校园永久池塘内的斑腿泛树蛙（Polypedates megacephalus）为实验对象,共61只（♀12,♂49）,测量其头体长、头长、吻宽、前肢长、后肢长等12项形态特征及体重来研究该物种的两性异形,并收集窝卵数和孵化数据分析雌性繁殖能力。结果表明：斑腿泛树蛙具有显著的两性异形,且雌性个体大于雄性个体;眼径、胫长和鼻间距在两性间无显著差异,头体长、头长、吻宽、吻长、眼间距、前肢长、后肢长、前臂及手长、足长和体重均具有显著差异;斑腿泛树蛙雌性个体产卵和孵化率受季节影响显著,其中4和5月窝卵数最多,6月卵孵化率最高;雌性怀卵数量与体长呈正相关关系。依据上述结果,本研究推测生育力选择是造成斑腿泛树蛙两性异形的主要因素,雌性个体通过增大个体体型来增加怀卵量,从而提高繁殖输出;斑腿泛树蛙繁殖期受季节影响,为更好地适应雨季的提前或推迟,在进化过程中形成了延长式繁殖的模式。     

Sexual size dimorphism in parasitoid wasps

Sexual dimorphism in body length and proportion of overlap between the ranges of body length for males and females were estimated for 361 species of parasitoid wasps from 21 families. In most species, females are generally larger than males, though the range of male and female sizes overlap. Species in the family Ichneumonidae differ significantly from species in other families in three ways: (1) ichneumonids on average are larger, (2) in most species, females are generally smaller than males, and (3) on average, proportion overlap between the ranges of body length for males and females is greater. At present, there is a paucity of life history data on parasitoid wasp species for which size dimorphism is known. Thus it is not clear why ichneumonids differ from species in other families. Possible evolutionary explanations for variation in dimorphism among parasitoid wasp species are discussed.     

Sexual dimorphism in lizard body shape: the roles of sexual selection and fecundity selection

Sexual dimorphism is widespread in lizards, with the most consistently dimorphic traits being head size (males have larger heads) and trunk length (the distance between the front and hind legs is greater in females). These dimorphisms have generally been interpreted as follows: (1) large heads in males evolve through male-male rivalry (sexual selection); and (2) larger interlimb lengths in females provide space for more eggs (fecundity selection). In an Australian lizard (the snow skink, Niveoscincus microlepidotus), we found no evidence for ongoing selection on head size. Trunk length, however, was under positive fecundity selection in females and under negative sexual selection in males. Thus, fecundity selection and sexual selection work in concert to drive the evolution of sexual dimorphism in trunk length in snow skinks.     

Sexual size dimorphism and timing of spring migration in birds

Sexually selected traits are limited by selection against those traits in other fitness components, such as survival. Thus, sexual selection favouring large size in males should be balanced by higher mortality of larger males. However, evidence from red-winged blackbirds (Agelaius phoeniceus) indicates that large males survive better than small males. A survival advantage to large size could result from males migrating north in early spring, when harsh weather favours large size for energetic reasons. From this hypothesis we predicted that, among species, sex differences in body size should be correlated with sex differences in timing of spring migration. The earlier males migrate relative to females, the larger they should be relative to females. We tested this prediction using a comparative analysis of data collected from 30 species of passerine birds captured on migration. After controlling for social mating system, we found that sexual size dimorphism and difference in arrival dates of males and females were significantly positively correlated. This result is consistent with the hypothesis that selection for survival ability promotes sexual size dimorphism (SSD), rather than opposes SSD as is the conventional view. If both natural selection and sexual selection favour large adult males, then limits to male size must be imposed before males become adults.     

Sexual size dimorphism and assortative mating in Carolina Wrens

ABSTRACT.   Sexual size dimorphism (SSD) may be due to sexual and natural selection, but identifying specific mechanisms that generate such dimorphism in a species is difficult. I examined SSD in Carolina Wrens ( Thryothorus ludovicianus ) by examining (1) the degree of SSD in the population and between pairs using five morphometrics, (2) assortative mating patterns based on size and age, and (3) relationships between size and longevity. Analysis revealed that males were significantly larger than females in all body measurements. For example, mass, bill, and wing measurements yielded a canonical variable that permitted separation of the sexes and linear classification functions correctly determined the sex of 95% (238/250) of all wrens measured. No evidence was found to suggest that SSD was related to resource partitioning. However, assortative mating trends based on morphometrics (e.g., wing length), positive associations between longevity and morphometrics (e.g., wing length in females and body size in males), and intense male-male contests for territorial resources year-round provide evidence that sexual selection may contribute to SSD in Carolina Wrens.     

Sexual selection and sexual size dimorphism in animals

Sexual selection is often considered as a critical evolutionary force promoting sexual size dimorphism (SSD) in animals. However, empirical evidence for a positive relationship between sexual selection on males and male-biased SSD received mixed support depending on the studied taxonomic group and on the method used to quantify sexual selection. Here, we present a meta-analytic approach accounting for phylogenetic non-independence to test how standardized metrics of the opportunity and strength of pre-copulatory sexual selection relate to SSD across a broad range of animal taxa comprising up to 95 effect sizes from 59 species. We found that SSD based on length measurements was correlated with the sex difference in the opportunity for sexual selection but showed a weak and statistically non-significant relationship with the sex difference in the Bateman gradient. These findings suggest that pre-copulatory sexual selection plays a limited role for the evolution of SSD in a broad phylogenetic context.     

Sexual dimorphism of body size and shell shape in European tortoises

Adult body size and shape were examined in almost 1400 individuals of the tortoises Testudo graeca , T. hermanni and T. marginata from Greece. The size at maturity was greater in females than in males in all three species. Maximum and mean adult sizes were also greater in females than in males in T. graeca and T. hermanni . Males grew to a larger size than females in T. marginata , and mean adult size was similar in the sexes in this species. Sexual dimorphism of shape (adjusted for size covariate) was shown in most of the characters examined, and the degree of this dimorphism differed significantly among the three species. Differences were related to their contrasting courtship behaviours: horizontal head movements and severe biting in T. marginata , vertical head bobs and carapace butting in T. graeca , and mounting and tail thrusting in T. hermanni . There was no difference in the frequency of observations of courtship or fighting among the three species, but courtship was about 10 times more common than combat in males. All species showed greatest courtship activity in autumn; copulation was rarely observed in T. hermanni (only 0.36% of courting males) and not seen in the other species in the field. Observations made throughout the activity season indicated that feeding was equally common in males and females in all three species. Differences in shape were more likely to be the result of sexual selection than of natural selection for fecundity. Detailed predictions are made for sexual dimorphism of other characters in these species.     

蒲河流域河流生境质量综合评价及其与水质响应关系

河流生境是河流生物赖以生存的环境,是维持河流生态完整性、维护河流健康的重要因素。本文结合蒲河流域环境特点,运用层次分析法建立了蒲河流域河流生境质量评价体系,对流域内25个河段的生境质量状况进行了综合评价,并进一步分析了河流生境综合评价指数与河流水质的相关关系。结果表明:(1)蒲河流域25个河段的生境质量状况差异显著,其中1个河段的生境质量等级为好,5个河段为较好等级,16个河段为一般等级,3个河段为较差等级。(2)生境综合评价指数与TP、NH4+-N、CODCr呈负相关,生境质量评价体系中其他指标也与水质指标具有相关性,表明生境质量是影响水质的重要因素。     

Sexual selection, sexual size dimorphism and Rensch's rule in Odonata

Odonata (dragonflies and damselflies) exhibit a range of sexual size dimorphism (SSD) that includes species with male-biased (males > females) or female-biased SSD (males < females) and species exhibiting nonterritorial or territorial mating strategies. Here, we use phylogenetic comparative analyses to investigate the influence of sexual selection on SSD in both suborders: dragonflies (Anisoptera) and damselflies (Zygoptera). First, we show that damselflies have male-biased SSD, and exhibit an allometric relationship between body size and SSD, that is consistent with Rensch's rule. Second, SSD of dragonflies is not different from unit, and this suborder does not exhibit Rensch's rule. Third, we test the influence of sexual selection on SSD using proxy variables of territorial mating strategy and male agility. Using generalized least squares to account for phylogenetic relationships between species, we show that male-biased SSD increases with territoriality in damselflies, but not in dragonflies. Finally, we show that nonagile territorial odonates exhibit male-biased SSD, whereas male agility is not related to SSD in nonterritorial odonates. These results suggest that sexual selection acting on male sizes influences SSD in Odonata. Taken together, our results, along with avian studies (bustards and shorebirds), suggest that male agility influences SSD, although this influence is modulated by territorial mating strategy and thus the likely advantage of being large. Other evolutionary processes, such as fecundity selection and viability selection, however, need further investigation.