西藏黑斑原繁殖群体两性异形研究

两性异形是指在同一种群内, 雌雄间的形态特征产生分化, 如在个体大小、局部形态构造、体色等方面呈现出差异的现象。为了解西藏黑斑原 (Glyptosternum maculatum) 雌雄间是否也存在两性异形, 在其繁殖期对性成熟个体进行了形态学测量及相关分析。结果表明: 西藏黑斑原繁殖群体间存在显著的雌雄异形, 一是雄性个体的体长、体重及特定体长下的尾长显著大于雌性个体; 二是在特定体长下, 雌性个体眼径、体高、躯干长以及背鳍、胸鳍、腹鳍、臀鳍、尾鳍长度均显著大于雄性。16个形态参数的主成分分析表明, 雌雄间的差异主要是由体型特征(包括身体各部分长度、各鳍长度等)及头部形态特征引起的, 贡献率达76.7%。对全长-体重方程中异速生长指数b的t检验表明, 繁殖期黑斑原雌性个体呈等速生长而雄性个体呈异速生长。     

西藏黑斑原繁殖群体两性异形研究（英文）

两性异形是指在同一种群内,雌雄间的形态特征产生分化,如在个体大小、局部形态构造、体色等方面呈现出差异的现象。为了解西藏黑斑原(Glyptosternum maculatum)雌雄间是否也存在两性异形,在其繁殖期对性成熟个体进行了形态学测量及相关分析。结果表明:西藏黑斑原繁殖群体间存在显著的雌雄异形,一是雄性个体的体长、体重及特定体长下的尾长显著大于雌性个体;二是在特定体长下,雌性个体眼径、体高、躯干长以及背鳍、胸鳍、腹鳍、臀鳍、尾鳍长度均显著大于雄性。16个形态参数的主成分分析表明,雌雄间的差异主要是由体型特征(包括身体各部分长度、各鳍长度等)及头部形态特征引起的,贡献率达76.7%。对全长-体重方程中异速生长指数b的t检验表明,繁殖期黑斑原雌性个体呈等速生长而雄性个体呈异速生长。     

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.     

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。     

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。     

实验室条件下唐鱼两性异形及其与游泳能力关系

为了解唐鱼两性异形及其与游泳能力关系,检测了性成熟阶段唐鱼躯干部和鱼鳍形态特征以及爆发游泳速度(U_burst)和临界游泳速度(U_crit)在雌雄之间的差异,旨在从形态适应角度探究长期进化中雌雄唐鱼各自面对选择压力所产生的游泳能力差异及其机制,从而为野生唐鱼保护提供基础数据.结果表明: 雌性唐鱼的体长、头高、头宽、尾鳍面积以及吻端至枕骨后末端、腹鳍起点至背鳍末端等长度均与雄性无显著差异.而体高、体宽、腹鳍起点至背鳍起点等反映腹腔大小的形态参数以及吻端至背鳍起点、吻端至臀鳍起点、枕骨后末端至背鳍起点等反映躯干部大小的形态参数均显示为雌性显著大于雄性,但头长以及胸鳍面积、腹鳍面积、背鳍面积和臀鳍面积均显示为雄性显著大于雌性.对所有数据进行主成分分析,结果显示第1主成分贡献率为74.2%,负载量较大的是体长、头长、头高、体高、头宽、体宽以及各鳍之间距离等主要反映唐鱼躯干整体特征的参数;第2主成分贡献率为15.7%,负载量较大的是胸鳍面积、腹鳍面积、背鳍面积和臀鳍面积等主要反映鱼鳍特征的参数.唐鱼性别在第1主成分上无法区分,但在第2主成分却可以明显区分.根据体宽、胸鳍面积、腹鳍面积、背鳍面积和臀鳍面积等建立的性别判别方程对雌雄判断准确率达到91.8%～92.5%.唐鱼游泳能力测定结果显示,雌性U_burst与雄性无显著差异,但U_crit显著小于雄性.以上结果表明,雌雄唐鱼两性异形主要集中在与游泳能力相关的鱼鳍特征上.相比雄性,雌性唐鱼虽然胸鳍等鱼鳍面积较小导致其U_crit小于雄性,却具有更长的躯干部以保证其同样具有较高的爆发游泳能力,从而有利于在流速波动很大的溪流中躲避捕食和进行其他应急活动;相比雌性,雄性唐鱼则具有较大的鱼鳍面积保证其U_crit高于雌性,以利于日常活动及在繁殖过程中追逐雌性等相对持久性游泳运动.     

中国林蛙种群形态特征及雌体生殖力的地理差异

为了比较中国林蛙(Rana chensinensis)不同种群的形态特征、两性异形和雌体生殖力等方面的地理变异,在中国林蛙分布范围的南部(河南郑州)和北部(内蒙古扎兰屯)采集标本共130只,测量了两性的体长、体重等26项形态特征和雌体的生殖力。结果表明:(1)中国林蛙的形态特征及两性异形方面存在显著的地理变异,雌性显著大于雄性,扎兰屯种群显著大于郑州种群;(2)中国林蛙形态特征的地理变异符合贝格曼定律,但四肢的形态变化规律不符合阿伦规律,体形较大的扎兰屯种群存在两性异形的形态特征数量少,但差异程度大,与伦施法则不符;(3)雌性是中国林蛙两性中形态特征地理变异最明显的一方,在对寒冷气候的适应过程中,雌性比雄性的体长和体重增加的程度更明显。由此可知,两性间身体大小变化趋势的不一致暗示不同性别的个体适应环境变化的策略可能存在较大差异,这是造成中国林蛙不同种群两性异形和雌体生殖力地理变异的主要原因。     

新疆沙虎的两性异形

通过测量和比较采自新疆且末县的新疆沙虎Teratoscincus przewalskii成体的体型和口宽等6个形态特征,研究了新疆沙虎的两性异形。研究共采集64只新疆沙虎(雌性26只,雄性38只),雌雄成体最小体长(SVL)分别为63.6 mm和59.7 mm。口宽、头宽、头高、眼间距和尾长5个局部形态特征均与体长呈显著正相关。新疆沙虎体长雌雄间无差异,其它身体形态特征仅口宽具有显著的两性差异,且口宽相对于体长呈异速生长,雌性增长速率大于雄性。新疆沙虎口宽的两性异形可能与两性间食性的差异有关,而体长和其它身体形态特征无显著两性差异则可能与性选择和自然选择的综合作用有关。     

卵胎生入侵种食蚊鱼的两性异形和雌性繁殖输出

检测了卵胎生入侵种食蚊鱼(Gambusia affinis)繁殖期个体大小和形态特征的两性异形以及雌性繁殖输出。结果表明,繁殖期,雌性个体的数量显著大于雄性个体,雌性个体的体长显著大于雄性个体,食蚊鱼属于偏向雌性的两性异形。以体长为协变量的One-way ANCOVA及后续的Tukey's检验显示,特定体长食蚊鱼的雌性个体的头宽、眼间距、体宽和体重均显著大于雄性个体;头长和尾鳍长的两性间差异不显著。6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65.1%的变异。头宽、眼间距、体宽和体重在第一主成分有较高的正负载系数(解释45.4%变异),头长在第二主成分有较高的负负载系数(解释19.7%变异)。食蚊鱼的繁殖输出与母体个体大小的线性回归显示,窝仔数和窝仔重均与母体体长、体重呈显著的正相关;食蚊鱼的繁殖输出与母体局部特征的线性回归显示,窝仔数和窝仔重均与母体头宽、眼间距和体宽呈显著的正相关。窝仔数与后代个体的平均体长呈显著的正相关、与后代个体的平均体重相关不显著,后代个体大小与数量不发生权衡。食蚊鱼繁殖期的性别比例、个体大小和局部形态特征的两性异形受生育力选择、性选择、生态位分化、食物竞争等多种选择压力的作用,也有利于该物种种群扩张和快速入侵。     

肇庆南草蜥形态、食性及运动表现的两性差异

通过测量头、尾、体和胃检,研究肇庆南草蜥Takydromus sexlineatus个体发育过程中两性异形和食性差异。南草蜥成体个体两性大小无显著差异,雄性头部显著大于雌性,两性头部大小异形可能是受到性选择压力的结果。雌雄个体食物生态位重叠度较高,两性生态位差异微弱,食性差异与两性头部异形无明显相关性。通过设计13种不同的环境温度,研究体温变化对南草蜥两性个体运动能力表现的影响。结果显示环境温度通过影响体温而影响南草蜥的运动表现,两性个体疾跑速均具有在低体温范围内随体温升高而加快、在高体温范围内随体温升高而降低的模式。在多数测试温度下,雄体的疾跑速均略大于雌体,但两者平均值在统计上无显著差异。体温对南草蜥的最大持续运动距离和停顿次数的影响显著,两性个体的疾跑速和最大持续运动距离呈显著正相关。雄性和雌性分别在26℃和30℃具有最佳的运动表现。     

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。     

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。     

A test of the Darwin–Fisher theory for the evolution of male secondary sexual traits in monogamous birds

The Darwin–Fisher theory proposes that the presence of male secondary sexual traits in monogamous birds is selected for by early season breeding of females that are in good condition. These early breeding females have high fecundity because of their good condition, and they select mates based on secondary sex traits. We tested whether this hypothesis may be responsible for the presence of male sexual ornaments in the great frigatebird, a socially and genetically monogamous seabird. Consistent with the Darwin–Fisher theory, we found that reproductive success declined over the season. However, males with more exaggerated ornaments were not chosen as mates earlier in the season than males with less exaggerated ornaments, and selection gradients on these ornaments were not significantly different from zero.     

Sexual selection is stabilizing selection in pupfish [Cyprinodon pecosensis)

One of the predictions of the 'good genes' model of sexual selection is that reproductively successful males with well-developed indicator traits should show smaller variances for non-indicator traits, that are not directly associated with mating success, when compared to non-breeding males and females. Thus sexual selection should reinforce stabilizing natural selection in reducing the variance in quantitative traits. This prediction is tested by analysing variation in eight morphological traits of breeding males, non-breeding males, and females of pupfish (Cyprinodon pecosensis). Breeding males tended to be less variable than non-breeding males for all principal component factors, and for all morphological traits except for depth, although these differences were statistically significant only for PC2, and PC5 and for pelvic fin length, number of pelvic fin rays and number of preopercular and preorbital pores. Similarly, breeding males tended to be less variable than females for all principal component factors and for all morphological traits except for number of preopercular pores. These differences were statistically significant for PC2, and for depth, pelvic fin length, number of preorbital pores and pectoral fin rays. The overall pattern of reduced variability in independent traits of breeding males revealed by principal component analysis is very consistent and highly significant (P<10⁵). These results support the prediction of the 'good genes' model and show that reproductively active males are subject to more severe stabilizing selection for several quantitative traits than non-breeding males and females. Thus sexual selection, through male-male competition, female choice, or an interaction of both selective processes, results in stabilizing selection on quantitative morphological traits.     

Patterns of sexual dimorphism in Mexican alligator lizards,Barisia imbricata

We compare morphological characteristics of male and female Barisia imbricata, Mexican alligator lizards, and find that mass, head length, coloration, incidence of scars from conspecifics, tail loss, and frequency of bearing the color/pattern of the opposite sex are all sexually dimorphic traits. Overall size (measured as snout–vent length), on the other hand, is not different between the two sexes. We use data on bite scar frequency and fecundity to evaluate competing hypotheses regarding the selective forces driving these patterns. We contend that sexual selection, acting through male‐male competition, may favor larger mass and head size in males, whereas large females are likely favored by natural selection for greater fecundity. In addition, the frequency of opposite‐sex patterning in males versus females may indicate that the costs of agonistic interactions among males are severe enough to allow for an alternative mating strategy. Finally, we discuss how sexual and natural selective forces may interact to drive or mask the evolution of sexually dimorphic traits.     

Factors driving extreme sexual size dimorphism of a sit-and-wait predator under low density

Sexual size dimorphism is often a likely outcome of the interplay between natural selection and sexual selection, with female size dictated primarily by natural selection that maximizes fecundity and male size by sexual selection that maximizes reproductive opportunities. Attention to male fitness has focused heavily on direct male-male conflict selecting for superior male size and/or fighting ability, although male reproductive traits vary immensely among animals. An alternative, advanced by Michael Ghiselin, posits highly mobile dwarf males as a strategy for finding relatively immobile females in low-density populations. Adult male crab spiders Misumena vatia , sit-and-wait predators, are strikingly smaller, much more active, and relatively longer-legged than their females. This size difference results largely from males having two fewer instars than females, which simultaneously results in marked protandry. Populations of M. vatia often were small and of low density, with a female-biased sex ratio and an operational sex ratio that changed strikingly over the season. Sexual selection through scramble competition (locating the female first) should favour this suite of characters in males of low-density populations. Although direct male-male contests favoured large males, the low densities of adult males and the dispersed, relatively immobile females led to low levels of direct intrasexual contest. Females exaggerated the problem of males in finding them by providing few cues to their presence, a pattern consistent with indirect mate choice. In addition to favouring high mobility, scramble competition favoured males that selected flowers attracting many prey, the sites most often occupied by females.     

Operational sex ratio and density do not affect directional selection on male sexual ornaments and behavior

Demographic parameters including operational sex ratio (OSR) and population density may influence the opportunity for, and strength of sexual selection. Traditionally, male-biased OSRs and high population densities have been thought to increase the opportunity for sexual selection on male sexual traits due to increased male competition for mates. Recent experimental evidence, however, suggests that male-biased OSRs might reduce the opportunity for sexual selection due to increased sexual coercion experienced by females. How OSR, density, and any resultant changes in the opportunity for sexual selection actually affect selection on male sexual traits is unclear. In this study, we independently manipulated OSR and density in the guppy (Poecilia reticulata) without altering the number of males present. We recorded male and female behavior and used DNA microsatellite data to assign paternity to offspring and estimate male reproductive success. We then used linear selection analyses to examine the effects of OSR and density on directional sexual selection on male behavioral and morphological traits. We found that females were pursued more by males in male-biased treatments, despite no change in individual male behavior. There were no differences in sexual behavior experienced by females or performed by males in relation to density. Neither OSR nor density significantly altered the opportunity for sexual selection. Also, Although there was significant multivariate linear selection operating on males, neither OSR nor density altered the pattern of sexual selection on male traits. Our results suggest that differences in either OSR or density (independent of the number of males present) are unlikely to alter directional evolutionary change in male sexual traits.     

No fecundity cost of female secondary sexual trait expression in the horned beetle Onthophagus sagittarius

Typically males bear the products of sexual selection in the form of ornaments and/or weapons used to compete for and attract females. Secondary sexual traits in females have been thought of as the product of correlated responses to sexual selection on males. However, there is increasing phylogenetic evidence that female secondary sexual traits can arise independently of selection on males, and may be subject to sexual selection. Theoretical models of the evolution of female ornamentation via male mate choice have assumed that females suffer a cost of ornament expression via reduced fecundity, and hence female ornaments are less likely to evolve than male ornaments. In the dung beetle Onthophagus sagittarius, there has been an independent evolutionary origin of horns in females that are qualitatively different from the horns produced by males. We use this system as a model to examine the costs of horn expression for females within a life-history context. We identified a longevity cost of reproduction for females that was independent of horn expression. Large females lived longer, and after controlling for lifespan, had a higher lifetime fecundity, and invested more heavily in maternal provisioning than did small females. We found no evidence of a cost to females of investment in horns. Rather, the rate of increase in fecundity and horn expression with body size were equal, so that absolute horn size provides an accurate indicator of body size and maternal quality. The effects we observe were independent of female contest competition and/or male mate choice, which were excluded in our experimental protocol. However, we speculate on the potential functional contributions female horns might make to female fitness.