啮齿运动胎仔数与生活史变量的关系

胎仔数是影响哺乳动物繁殖率的基本参数,与动物的生活史变量密切相关,胎仔数及其相关的生活史变量,包括后代的质量、幼体的生存、母体的体重及母体的生存等,共同影响繁殖适合度。简述了胎仔数与生活史变量关系的研究方法及研究对象的选择,着重介绍了胎仔数与幼体和母体生活史变量的关系：胎仔数与后代的质量呈负相关,后代的质量又决定了幼体的生存;胎仔数与母体体重相关不显著,而且可能对母体的生存产生负面影响。有关胎仔数与其生活史变量的关系还有待于正派 探索,更多先进技术手段与方法的交叉运用将补充和完善胎仔数与其生活史变量的关系有待于进一步的探索,更多先进技术手段与方法的交叉运用将补充和完善胎仔数与其生活史变量的关系还有待于进一步的探索,更多先进技术手段与方法的交叉运用将补充和完善胎仔数研究的内容。     

高体重布氏田鼠产仔数较多但繁殖输出及氧化损伤不受影响

体重可影响动物几乎所有的生物学变量。高体重双亲通常产生较大胎仔数。繁殖过程代价很高,可能伴随着氧化损伤。为比较双亲体重对繁殖期能量学特征、繁殖输出和氧化损伤的影响,检测了高体重组(雌性:51. 5 g ± 1. 6 g;雄性:60. 4 g ±2. 5 g)和低体重组(雌性:35. 5 g ± 1. 2 g;雄性:49. 6 g ± 2. 8 g)布氏田鼠繁殖过程中母体的体重和摄食量,分娩时的胎仔数和胎仔总重,及后代断乳时母体的身体成分、激素含量(血清瘦素和催乳素)和氧化损伤(血清丙二醛、蛋白质羰基和肝脏丙二醛含量)。结果显示:(1)高体重组妊娠末期的母体体重增量显著高于低体重组;(2)高体重组母体的出生胎仔数显著高于低体重组,但出生及断乳时的平均胎仔重、胎仔总重和母体繁殖期间的能量摄入无显著差异; (3)血清激素含量、身体成分、身体脂肪重量及氧化损伤指标均无组间差异。结果表明,高体重布氏田鼠可产生较多的出生胎仔数,但母体并不通过摄入更多的能量来保证其繁殖输出,对氧化损伤也没有影响。这些结果对于理解不同体重的动物在繁殖期间的能量策略以及繁殖与生存之间的权衡等生活史理论具有重要意义。     

剃毛和增加胎仔数对KM 小鼠哺乳期能量收支的影响

为探讨最大持续能量收支限制的因素和生理机理,本文测定了增加胎仔数和背部剃毛的KM 小鼠的哺乳
期摄食量和繁殖输出。基础代谢率(BMR)以封闭式流体压力呼吸计测定。结果发现,增加胎仔数对哺乳期体
重、摄食量、热传导率、BMR 和胎仔重的影响不显著;与非剃毛对照组相比,剃毛使哺乳高峰期日平均摄食量
增加了13.8% (P<0.001)、BMR 增加了18.1% (P< 0.01)、热传导增加了30.8% (P< 0.01),但剃毛对体
重、胎仔数和胎仔重的影响不显著;胎仔数与断乳时胎仔重显著正相关,与幼体平均体重显著负相关。BMR 与
母体体重和胎仔重显著正相关。这些结果表明,KM 小鼠哺乳期能量收支受到了限制,剃毛显著增强了KM 小鼠
的散热能力,但未影响繁殖输出;支持“外周限制假说”,不符合“热耗散限制假说”。     

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。     

温度和增加胎仔数对大绒鼠哺乳期能量代谢的影响

为了阐明温度和增加胎仔数对大绒鼠Eothenomys miletus哺乳期能量代谢的影响,本研究测定了在不同温度条件下增加胎仔数(比正常胎仔数多),大绒鼠的摄食量、胎仔数、胎仔质量、静止代谢率、非颤抖性产热和乳腺质量。结果表明:不同胎仔数对大绒鼠的摄食量、胎仔质量和产热能力没有影响。低温增加了母体的摄食量和产热能力,断奶时低温组的胎仔质量显著低于常温组。低温组和常温组大绒鼠的乳腺质量差异无统计学意义。研究结果说明低温可以增加大绒鼠摄食量,但是对乳腺质量没有影响,表明大绒鼠哺乳期的持续能量摄入上限可能受到乳腺分泌乳汁的限制,支持外周限制假说。     

yan蜓头、体大小的两性异形和雌体繁殖

报道了yan蜓(Sphenomorphus indicus)头、体大小的两性异形和雌性繁殖。性成熟雌体大于雄体。雄性成体头长大于雌性成体，但头宽与雌性成体无显著差异。初生幼仔的头长和头宽无两性差异。雄性幼体头长和头宽大于雌性幼体。设置SVL恒定时，雄性幼体和雄性成 体的头长和头宽无显著差异，雌性幼体的头长和头宽大于雌性成体。初生幼仔具有相对较大的头部。产仔雌体的最小SVL为67.7 mm，大于此SVL的雌体均年产单窝仔。平均窝仔数、窝仔重和幼仔重分别为7.2(3-11)、3.34(1.30-5.19)和0.48(0.36-0.58)g。用卵黄沉积卵巢卵和输卵管计数的窝仔数比用幼仔计数的窝仔数多约1.0个后代。幼仔体重与雌体SVL无关。相对窝仔重与雌体SVL边缘性地呈正相关。窝仔数、窝仔重与雌体SVL呈正相关，幼仔体重与窝仔数呈负相关。窝仔数与雌体状态无关。     

蝘蜓头、体大小的两性异形和雌体繁殖

报道了蜓 (Sphenomorphusindicus)头、体大小的两性异形和雌性繁殖。性成熟雌体大于雄体。雄性成体头长大于雌性成体 ,但头宽与雌性成体无显著差异。初生幼仔的头长和头宽无两性差异。雄性幼体头长和头宽大于雌性幼体。设置SVL恒定时 ,雄性幼体和雄性成体的头长和头宽无显著差异 ,雌性幼体的头长和头宽大于雌性成体。初生幼仔具有相对较大的头部。产仔雌体的最小SVL为 6 7 7mm ,大于此SVL的雌体均年产单窝仔。平均窝仔数、窝仔重和幼仔重分别为 7 2 ( 3～ 11)、 3 34( 1 30～ 5 19)和 0 48( 0 36～ 0 5 8)g。用卵黄沉积卵巢卵和输卵管计数的窝仔数比用幼仔计数的窝仔数多约 1 0个后代。幼仔体重与雌体SVL无关。相对窝仔重与雌体SVL边缘性地呈正相关。窝仔数、窝仔重与雌体SVL呈正相关 ,幼仔体重与窝仔数呈负相关。窝仔数与雌体状态无关。     

胎仔数与父本缺失对棕色田鼠幼仔体重发育的影响

室内饲养条件下,测量了出生后不同发育阶段棕色田鼠Microtus mandarinus的体重,并探讨了胎仔数(分别为1只、2只、3只和4只)及父本缺失(母鼠单独抚育)对幼仔体重发育的影响.结果表明,棕色田鼠出生后第一周体重的瞬时生长率最高,此后逐步下降;出生后28～35 d,体重增益最大(P<0.05).出生后7 d,不同胎仔数的体重没有明显差异,但至断乳时(出生后21 d),胎仔数为2只的幼仔平均体重明显高于其它胎仔数的平均体重(P<0.05).与双亲抚育相比,母鼠单独抚育的幼仔在断乳时的体重明显下降(P<0.05).这些结果说明,哺乳期内棕色田鼠幼仔的体重发育与胎仔数有关.由于棕色田鼠是单配制,双亲育幼,父本雄鼠的缺失减少了亲本投资,影响了幼仔的身体发育.     

升温对北草蜥雌体繁殖、卵孵化及幼体特征的影响

在围栏条件下,比较升温和对照处理北草蜥(Takydromus septentrionalis)繁殖、卵孵化及幼体特征的差异,以揭示升温对其繁殖生活史特征的作用。升温处理对北草蜥母体体温有显著影响,但并不影响其繁殖输出。升温显著影响卵孵化期和幼体的运动能力,但不影响幼体大小等形态特征。升温条件下孵出的幼体运动能力较弱。结果表明,北草蜥母体能耐受短期的环境增温,维持相对恒定的繁殖输出;升温能影响幼体的功能表现,进而可能改变后代适合度。     

肝毛细线虫对雌性布氏田鼠繁殖参数的影响

2005年5月,在内蒙古锡林郭勒盟阿巴嘎旗北部,研究了肝毛细线虫(Capillaria hepatica)对典型草原区雌性布氏田鼠(Lasiopodomys brandtii)繁殖参数的影响。采用标准夹线法捕获鼠类,对捕获的鼠类进行常规生物学解剖,根据虫卵有无确定肝毛细线虫病感染情况,记录鼠类名称、体长、体重、胴体重、繁殖特征以及肝毛细线虫病感染情况。由于体重是划分鼠类年龄的常用指标之一,结合布氏田鼠的繁殖特征研究数据,采用25.1~55.0 g之间的雌性个体作为本研究分析样本,并将其分为25.1~35.0 g、35.1~45.0 g和45.1~55.0 g体重(年龄)组。采用卡方检验比较分析同一体重(年龄)组内,肝毛细线虫病感染情况与雌性布氏田鼠妊娠率的关系,T检验分析感染情况与胎仔数的关系。结果显示,在各个体重(年龄)组中,感染肝毛细线虫组布氏田鼠雌鼠妊娠率均略低于未感染组,但感染情况与妊娠情况无显著相关关系(P0.05);感染肝毛细线虫布氏田鼠胎仔数低于未感染布氏田鼠,感染情况与胎仔数有显著相关关系(P0.05)。结果表明,肝毛细线虫病对布氏田鼠妊娠率无明显影响,但对布氏田鼠胎仔数有明显的负面影响。     

Optimal allocation of reproductive effort: manipulation of offspring number and size in the bank vole

The number of offspring attaining reproductive age is an important measure of an individual's fitness. However, reproductive success is generally constrained by a trade-off between offspring number and quality. We conducted a factorial experiment in order to study the effects of an artificial enlargement of offspring number and size on the reproductive success of female bank voles (Clethrionomys glareolus). We also studied the effects of the manipulations on growth, survival and reproductive success of the offspring. Potentially confounding effects of varying maternal quality were avoided by cross-fostering. Our results showed that the number of offspring alive in the next breeding season was higher in offspring number manipulation groups, despite their smaller body size at weaning. Offspring size manipulation had no effect on offspring growth or survival. Further, the first litter size of female offspring did not differ between treatments. In conclusion, females may be able to increase the number of offspring reaching reproductive age by producing larger litters, whereas increasing offspring size benefits neither the mother nor the offspring.     

SELECTION ON MOTHERS AND OFFSPRING: WHOSE PHENOTYPE IS IT AND DOES IT MATTER?

Reproductive and early life-history traits can be considered aspects of either offspring or maternal phenotype, and their evolution will therefore depend on selection operating through offspring and maternal components of fitness. Furthermore, selection at these levels may be antagonistic, with optimal offspring and maternal fitness occurring at different phenotypic values. We examined selection regimes on the correlated traits of birth weight, birth date, and litter size in Soay sheep (Ovis aries) using data from a long-term study of a free-living population on the archipelago of St. Kilda, Scotland. We tested the hypothesis that selective constraints on the evolution of the multivariate phenotype arise through antagonistic selection, either acting at offspring and maternal levels, or on correlated aspects of phenotype. All three traits were found to be under selection through variance in short-term and lifetime measures of fitness. Analysis of lifetime fitness revealed strong positive directional selection on birth weight and weaker selection for increased birth date at both levels. However, there was also evidence for stabilizing selection on these traits at the maternal level, with reduced fitness at high phenotypic values indicating lower phenotypic optima for mothers than for offspring. Additionally, antagonistic selection was found on litter size. From the offspring's point of view it is better to be born a singleton, whereas maternal fitness increases with average litter size. The decreased fitness of twins is caused by their reduced birth weight; therefore, this antagonistic selection likely results from trade-offs between litter size and birth weight that have different optimal resolutions with respect to offspring and maternal fitness. Our results highlight how selection regimes may vary depending on the assignment of reproductive and early life-history traits to either offspring or maternal phenotype.     

Maternal investment during pregnancy in wild meerkats

Maternal investment in offspring development is a major determinant of the survival and future reproductive success of both the mother and her young. Mothers might therefore be expected to adjust their investment according to ecological conditions in order to maximise their lifetime fitness. In cooperatively breeding species, where helpers assist breeders with offspring care, the size of the group may also influence maternal investment strategies because the costs of reproduction are shared between breeders and helpers. Here, we use longitudinal records of body mass and life history traits from a wild population of meerkats (Suricata suricatta) to explore the pattern of growth in pregnant females and investigate how the rate of growth varies with characteristics of the litter, environmental conditions, maternal traits and group size. Gestational growth was slight during the first half of pregnancy but was marked and linear from the midpoint of gestation until birth. The rate of gestational growth in the second half of pregnancy increased with litter size, maternal age and body mass, and was higher for litters conceived during the peak of the breeding season when it is hot and wet. Gestational growth rate was lower in larger groups, especially when litter size was small. These results suggest that there are ecological and physiological constraints on gestational growth in meerkats, and that females may also be able to strategically adjust their prenatal investment in offspring according to the likely fitness costs and benefits of a particular breeding attempt. Mothers in larger groups may benefit from reducing their investment because having more helpers might allow them to lower reproductive costs without decreasing breeding success.     

Offspring growth, survival and reproductive success in the bank vole: a litter size manipulation experiment

To estimate the optimality of brood size, it is essential to study the effects of brood size manipulation on offspring survival and reproductive success. Moreover, testing the generality of the hypothesis of reproductive costs requires experimental data from a diversity of organisms. Here I present data on the growth, survival and reproductive success of bank vole Clethrionomys glareolus individuals from manipulated litters. Furthermore, the survival of mothers whose litter size was manipulated was studied. At weaning, the mean weight of pups from enlarged litters was lower and from reduced litters higher compared to control litters. After winter, at the start of the breeding season, individuals from enlarged litters, especially males, were still lighter than individuals from the other two treatments. Litter enlargements did not increase the number of reproducing female offspring per mother, nor did the litter sizes of female offspring differ between treatments. There were no differences between treatments in winter survival of offspring after weaning, but among female offspring, weaning weight explained the survival probabilities over winter. A higher weight of females at winter determined the probability of starting to reproduce in spring. The survival of mothers did not seem to be influenced by litter manipulation performed the previous year. According to the results, mothers nursing enlarged or reduced litters do not gain any fitness benefits in terms of number of offspring surviving to breeding. The results are consistent with the majority of experiments conducted in birds, which have found costs of enlarged brood appearing as offspring trade-offs rather than parent trade-offs. Received: 14 December 1997 / Accepted: 1 March 1998     

PROXIMATE AND ULTIMATE CONTROLS ON LIFE-HISTORY VARIATION: THE EVOLUTION OF LITTER SIZE IN WHITE-FOOTED MICE (PEROMYSCUS LEUCOPUS)

Recruitment of litter-mates of nest-box-inhabiting white-footed mice was monitored to study the evolution of litter size. The frequency distribution of litter sizes was nonsymmetrical, and the most frequent litter size was less than the optimum. This was not the result of differential parental survival, which was independent of litter size produced. Recruitment remained constant or increased slightly to a peak in litters of five young, and then dropped precipitously for larger litters. The single optimum litter size of five did not appear to have any physiological correlates. Instead, the equally low probability of successful recruitment of any young from any given litter may have given rise to a bet-hedging strategy of frequent iterated reproductions. A theoretical analysis of optimal parental investment in offspring was initiated under the assumption that optimal brood size represents a maximization of differences between age-specific costs and benefits of reproduction, both of which should be measured in constant currency of inclusive fitness. In the past, benefit has been measured by current fecundity, and cost by residual reproductive value. However, reproductive value is an appropriate estimate of inclusive fitness only for organisms in which parental investment has little effect on the subsequent survival of offspring to reproductive age. Reproductive value weighted by offspring survival and devalued by the degree of genetic relatedness defines a new currency, replacement value, which is more appropriate for evaluating the costs and benefits of parent-offspring conflict over parental investment in current as opposed to future young. Total parent-offspring conflict intensifies with increases in current brood size. For species with severe reproductive constraints, such as post-partum estrus in white-footed mice, such conflict may force parents to curtail investment in current offspring at or near parturition of subsequent litters, even if that means reducing the survival of current young.     

Costs of reproduction and terminal investment by females in a semelparous marsupial

Evolutionary explanations for life history diversity are based on the idea of costs of reproduction, particularly on the concept of a trade-off between age-specific reproduction and parental survival, and between expenditure on current and future offspring. Such trade-offs are often difficult to detect in population studies of wild mammals. Terminal investment theory predicts that reproductive effort by older parents should increase, because individual offspring become more valuable to parents as the conflict between current versus potential future offspring declines with age. In order to demonstrate this phenomenon in females, there must be an increase in maternal expenditure on offspring with age, imposing a fitness cost on the mother. Clear evidence of both the expenditure and fitness cost components has rarely been found. In this study, we quantify costs of reproduction throughout the lifespan of female antechinuses. Antechinuses are nocturnal, insectivorous, forest-dwelling small (20-40 g) marsupials, which nest in tree hollows. They have a single synchronized mating season of around three weeks, which occurs on predictable dates each year in a population. Females produce only one litter per year. Unlike almost all other mammals, all males, and in the smaller species, most females are semelparous. We show that increased allocation to current reproduction reduces maternal survival, and that offspring growth and survival in the first breeding season is traded-off with performance of the second litter in iteroparous females. In iteroparous females, increased allocation to second litters is associated with severe weight loss in late lactation and post-lactation death of mothers, but increased offspring growth in late lactation and survival to weaning. These findings are consistent with terminal investment. Iteroparity did not increase lifetime reproductive success, indicating that terminal investment in the first breeding season at the expense of maternal survival (i.e. semelparity) is likely to be advantageous for females.     

Females allocate differentially to offspring size and number in response to male effects on female and offspring fitness

Female investment in offspring size and number has been observed to vary with the phenotype of their mate across diverse taxa. Recent theory motivated by these intriguing empirical patterns predicted both positive (differential allocation) and negative (reproductive compensation) effects of mating with a preferred male on female investment. These predictions, however, focused on total reproductive effort and did not distinguish between a response in offspring size and clutch size. Here, we model how specific paternal effects on fitness affect maternal allocation to offspring size and number. The specific mechanism by which males affect the fitness of females or their offspring determines whether and how females allocated differentially. Offspring size is predicted to increase when males benefit offspring survival, but decrease when males increase offspring growth rate. Clutch size is predicted to increase when males contribute to female resources (e.g. with a nuptial gift) and when males increase offspring growth rate. The predicted direction and magnitude of female responses vary with female age, but only when per-offspring paternal benefits decline with clutch size. We conclude that considering specific paternal effects on fitness in the context of maternal life-history trade-offs can help explain mixed empirical patterns of differential allocation and reproductive compensation.     

Senescence and costs of reproduction in the life history of a small precocial species

Species following a fast life history are expected to express fitness costs mainly as increased mortality, while slow‐lived species should suffer fertility costs. Because observational studies have limited power to disentangle intrinsic and extrinsic factors influencing senescence, we manipulated reproductive effort experimentally in the cavy (Cavia aperea) which produces extremely precocial young. We created two experimental groups: One was allowed continuous reproduction (CR) and the other intermittent reproduction (IR) by removing males at regular intervals. We predicted that the CR females should senesce (and die) earlier and produce either fewer and/or smaller, slower growing offspring per litter than those of the IR group. CR females had 16% more litters during three years than IR females. CR females increased mass and body condition more steeply and both remained higher until the experiment ended. Female survival showed no group difference. Reproductive senescence in litter size, litter mass, and reproductive effort (litter mass/maternal mass) began after about 600 days and was slightly stronger in CR than IR females. Litter size, litter mass, and offspring survival declined with maternal age and were influenced by seasonality. IR females decreased reproductive effort less during cold seasons and only at higher age than CR females. Nevertheless, offspring winter mortality was higher in IR females. Our results show small costs of reproduction despite high reproductive effort, suggesting that under ad libitum food conditions costs depend largely on internal regulation of allocation decisions.     

Optimal size and number of propagules: allowance for discrete stages and effects of maternal size on reproductive output and offspring fitness

Existing optimality models of propagule size and number are not appropriate for many organisms. First, existing models assume a monotonically increasing offspring fitness/propagule size relationship. However, offspring survival during certain stages may decrease with increasing propagule size, generating a peaked offspring fitness/propagule size function (e.g., egg size in oxygen-limited aquatic environments). Second, existing models typically do not consider maternal effects on total reproductive output and the expression of offspring survival/propagule size relationships. However, larger females often have greater total egg production and may provide better habitats for their offspring. We develop a specific optimality model that incorporates these effects and test its predictions using data from salmonid fishes. We then outline a general model without assuming specific functional forms and test its predictions using data from freshwater fishes. Our theoretical and empirical results illustrate that, when offspring survival is negatively correlated with propagule size, optimal propagule size is larger in better habitats. When larger females provide better habitats, their optimal propagule size is larger. Nevertheless, propagule number should increase more rapidly than propagule size for a given increase in maternal size. In the absence of density dependence, females with greater relative reproductive output (i.e., for a given body size) should produce more but not larger propagules.     

Determinants of reproductive success in female adders,Vipera berus

Summary Female lifetime reproductive success in a small population of individually-marked adders in southern Sweden was studied over a period of seven years. Reproductive characteristics varied little from year to year and were consistent through time in individual females. Most females mature at four years of age and reproduce every two years. The total number of offspring produced by a female depends on her adult body size (and thus, litter size) and longevity (and thus, number of litters per lifetime). Adult body size in females is influenced mainly by subadult growth rates. Offspring size depends on maternal body size and a tradeoff between offspring size and offspring number. Maternal age does not affect litter sizes and offspring sizes except through ontogenetic changes in maternal body size.Survival of females after parturition is low because of the high energy costs of reproduction, compounded by low feeding rates of gravid females because of their sedentary behaviour at this time. About one-half of females produce only a single litter during their lifetimes, although some females live to produce four or five litters. On a proximate basis, rates of energy accumulation for growth (in subadults) and reproduction (in adults) may be the most important determinants of fitness in female adders.