克隆植物的无性与有性繁殖对策

许多植物同时具有克隆生长与有性繁殖,两种繁殖方式间的平衡在不同物种间以及同一物种内不同种群间变化很大。旺盛的克隆生长可能会从多方面影响生活史进化。首先,许多克隆植物的有性繁殖与更新程度都很低,甚至有一些植物由于克隆生长而几乎完全放弃了有性过程,从而影响到克隆植物对局域环境的适应和地理范围进化。其次,克隆生长增大花展示进而增加了对传粉者的吸引,同时也增加了同株异花授粉的风险,而同株异花授粉往往会导致植物雄性和雌性适合度的下降。因此,克隆植物的空间结构与交配方式间可能存在着协同进化关系。最后,克隆生长与有性繁殖间可能存在着权衡关系:对克隆生长的资源投入将会减少对有性繁殖的资源投入。这种权衡关系可能是由环境条件、竞争力度、植物寿命和遗传等因素决定的。如果不同的繁殖方式是植物在不同环境下采取的适应性对策,那么我们可以预期:在波动和竞争力度大的生境中,植物应将大部分的繁殖资源分配给有性繁殖;而在相对稳定的环境中,克隆繁殖应该占据优势地位。但是自然选择对两种繁殖方式的选择结果是什么,以及控制这两种方式间平衡的生态和遗传因子究竟有哪些,到底是克隆生长单向地影响了植物的有性繁殖,还是与有性过程相伴随的选择压力同时塑造了植物的克隆习性?目前尚不清楚。同时从无性与有性繁殖两个方面综合考察克隆植物的繁殖对策是今后亟待加强的工作。     

EGG FREEZING: A BREAKTHROUGH FOR REPRODUCTIVE AUTONOMY?

This article describes the relatively new technology of freezing human eggs and examines whether egg freezing, specifically when it is used by healthy women as 'insurance' against age-related infertility, is a legitimate exercise of reproductive autonomy. Although egg freezing has the potential to expand women's reproductive options and thus may represent a breakthrough for reproductive autonomy, I argue that without adequate information about likely outcomes and risks, women may be choosing to freeze their eggs in a commercially exploitative context, thus undermining rather than expanding reproductive autonomy.     

Patterns of reproductive effort with time since last fire in Florida scrub plants

Abstract. In periodically burned ecosystems, fire frequency may be an important selective pressure for the evolution of plant reproductive allocation patterns. We evaluated this hypothesis for Florida (USA) scrub plants by developing three models of reproductive effort with time since last fire given assumptions concerning seed dormancy and seedling establishment. We then examined reproductive effort of five woody, resprouting shrubs at sites representing nine times since last fire (ranging from 0–64 yr). All species showed significant patterns with time since fire in percentage of stems reproductive and fruit production. Stems of all species needed to attain a minimum size before flowering. Four species had the greatest level of reproductive effort (fruit biomass/above-ground biomass) within 5 yr post-fire and best fit the Early Peak Model of reproductive effort (i.e. between-fire seedling recruitment or seed dormancy). A fifth species best fit the Broad Peak Model (i.e. immediate post-fire seedling establishment), peaking in reproductive effort at 7 yr post-fire. Both of these models are based on somewhat variable fire-return intervals, suggesting that the frequency of scrub fires may have been too unpredictable to select for reproductive allocation patterns precisely reflecting particular fire-return intervals. Early peaks in post-fire reproductive effort may be a bet-hedging strategy to allow for greater chances of seedling establishment and survival.     

The Burden of Motherhood: The Effect of Reproductive Load on Female Lizard Locomotor,Foraging, and Social Behavior

The costs of reproduction, involving demands associated with both current and future reproductive efforts, may place a substantial burden on females. However, animals may minimize these costs by modifying their behavior across the reproductive cycle. We examined the effects of reproductive load on three types of behavior (locomotion, foraging, and social displays) in green anole lizards (Anolis carolinensis) by comparing egg, follicle, and oviduct mass and volume with field observational data. We found that female locomotor and social display behaviors decreased as reproductive load increased, suggesting behavioral modification in these traits, but we detected no relationship between foraging and reproductive load. We also examined these relationships across eight Anolis species using a phylogenetically informed analysis and found no associations between the evolution of reproductive load and any of the three behaviors. These results suggest that the evolution of increased reproductive load is not associated with the interspecific variation in behavior across the anoles and may result from varying life history traits or selective ecological pressures across species.     

Sex-specific associations between reproductive output and hematozoan parasites of American kestrels

Parasites have the potential to decrease reproductive output of hosts by competing for nutrients or forcing hosts to invest in immune function. Conversely, reproductive output may affect parasite loads if hosts allocate resources to reproduction such that allocation to immune function is compromised. Both hypotheses implicitly have a temporal component, so we sampled parasites both before and after egg laying to examine the relationship between reproductive output (indexed using a combined measure of clutch size, egg volume, and initiation date) and blood parasite loads of American kestrels (Falco sparverius). Parasite loads measured prior to egg laying had no adverse effects on subsequent reproductive output. Females that previously had large reproductive outputs subsequently had lower parasite intensities than those whose outputs were smaller, suggesting that females were capable of allocating energy to both forming clutches and reducing parasite loads. Because male kestrels provide most of their mate's energetic needs before, during, and after egg laying, mate choice by females may have consequences for their parasite loads. Females choosing high-quality mates may not only have increased reproductive output, but may also obtain sufficient resources from their mates to enable them to reduce their parasite burdens. Males whose mates had large reproductive outputs were more likely to subsequently be parasitized and have more intense infections. For individual males sampled both before and after egg laying, those whose mates had larger reproductive outputs were also more likely to become parasitized, or remain parasitized, between sampling periods. Increased parasite loads of males may be one mechanism by which the costs of reproduction are paid.     

Reproductive compensation

The reproductive compensation hypothesis says that individuals constrained by ecological or social forces to reproduce with partners they do not prefer compensate for likely offspring viability deficits. The reproductive compensation hypothesis assumes that (i) pathogens and parasites evolve more rapidly than their hosts, (ii) mate preferences predict variation in health and viability of offspring, (iii) social and ecological factors keep some individuals from mating with their preferred partners (some are constrained to mate with partners they do not prefer), (iv) all individuals may be induced to compensate, so that (v) variation in compensation is due to environmental and developmental factors affecting between-individual abilities to express compensatory mechanisms. Selection favouring compensation may act through variation in prezygotic physiological mechanisms, zygotic mechanisms, or parental care to eggs or young that enhance offspring health, increasing the likelihood that some offspring survive to reproductive age, often at a survival cost to the parents. Compensation may be through increased number of eggs laid or offspring born, a compensatory effort working during a single reproductive bout that sometimes will match the number of offspring surviving to reproductive age produced by unconstrained parents during the same bout. The reproductive compensation hypothesis therefore predicts trade-offs in components of fitness for breeders, such that parents constrained to mating with a nonpreferred partner, but who compensate sometimes match their current productivity (number of offspring at reproductive age) to unconstrained parents (those breeding with their preferred partners), and, when all else is equal, die faster than unconstrained parents. The reproductive compensation hypothesis emphasizes that reproductive competition is not just between constrained and unconstrained individuals, but also among constrained individuals who do and do not compensate. The reproductive compensation hypothesis may thus explain previously unexplained between-population and within-population, between-individual variation in reproductive success, survival, physiology and behaviour.     

Energy metabolism and the evolution of reproductive suppression in the human female

Reproduction places severe demands on the energy metabolism in human females. When physical work entails higher energy expenditure, not enough energy will be left for the support of the reproductive processes and temporal suppression of the reproductive function is expected. While energy needed for reproduction may be obtained by increases in energy intake, utilization of fat reserves, or reallocation of energy from basal metabolism, several environmental or physiological constraints render such solutions unlikely. For human ancestors increases in energy intake were limited by availability of food, by labor of food preparation and by metabolic ceilings to energy assimilation. Energy stored as fat may support only a fraction of the requirements for reproduction (especially lactation). Effects of intense physical activity on basal metabolism may also interfere with fat accumulation during pregnancy. Finally, the female physiology may experience demands on increasing the basal metabolism as a consequence of physical activity and, at the same time, on decreasing the basal metabolism, when energy to support the ongoing pregnancy or lactation is inadequate. The resulting metabolic dilemmas could constitute a plausible cause for the occurrence of reproductive suppression in response to physical activity. It is, therefore, likely that allocating enough energy to the reproductive processes during periods when energy expenditure rises may be difficult due to physiological and bioenergetic constraints. Females attempting pregnancy in such conditions may compromise their lifetime reproductive output. A reproductive suppression occurring in low energy availability situations may thus represent an adaptive rather then a pathological response.     

Changing motivations during migration: linking movement speed to reproductive status in a migratory large mammal

A challenge in animal ecology is to link animal movement to demography. In general, reproducing and non-reproducing animals may show different movement patterns. Dramatic changes in reproductive status, such as the loss of an offspring during the course of migration, might also affect movement. Studies linking movement speed to reproductive status require individual monitoring of life-history events and hence are rare. Here, we link movement data from 98 GPS-collared female moose (Alces alces) to field observations of reproductive status and calf survival. We show that reproductive females move more quickly during migration than non-reproductive females. Further, the loss of a calf over the course of migration triggered a decrease in speed of the female. This is in contrast to what might be expected for females no longer constrained by an accompanying offspring. The observed patterns demonstrate that females of different reproductive status may have distinct movement patterns, and that the underlying motivation to move may be altered by a change in reproductive status during migration.     

Effects of environmental enrichment on reproduction

Although there have been few demonstrations of a direct empirical relationship between environmental enrichment and reproductive success in captive animals, indirect and anecdotal evidence indicates the importance of physical and temporal complexity for reproduction. We discuss three major mechanisms through which environmental enrichment that specifically increases the complexity of an animal's surroundings may influence reproductive physiology and behavior: developmental processes, modulation of stress and arousal, and modification of social interactions. In complex environments developing animals learn that performing active behavior produces appropriate functional outcomes. Learning to control their environment influences their ability to adapt to novel situations, which may profoundly influence their reproductive behavior as adults in breeding situations. Chronic stress may compromise reproductive physiology and behavior; enrichment reduces stress by providing increased opportunity for behavioral coping responses. However, some degree of acute stress may be beneficial for reproduction by maintaining an animal's level of responsiveness to socio-sexual stimuli necessary for sexual arousal and reproductive activation. Finally, environmental enrichment may influence reproductive success by stabilizing social groups, reducing aggression and increasing affiliative and play behaviors. It is concluded that multi-variate multi-institutional behavioral research in zoos will play an increasingly important role in the successful captive propagation of many species by closely examining relationships between environmental variables and reproductive potential of individual animals. © 1994 Wiley-Liss, Inc.     

Epigenetic perspectives of safety in assisted reproductive technologies

To date, a wide range of assisted reproductive technologies is available for patients with impaired fertility. In general, the current methods of reproductive medicine are considered safe and do not significantly increase the frequency of birth of children with diseases or congenital malformations. However, the evidence has been accumulating in literature on higher risk of genomic imprinting diseases (Beckwith-Wiedemann and Angelman syndromes) as a result of using assisted reproductive technologies. In most cases examined, the appearance of these syndromes was explained by defective methylation status of imprinted genes. It has been suggested that manipulations with gametes and embryos during the period of total epigenetic modification of their genomes may act as potential risk factors of assisted reproductive technologies. Moreover, overcoming many natural reproductive barriers may contribute to the development of some pathological phenotypes. The review summarizes current views on epigenetic risk factors associated with assisted reproductive technologies.     

Reproductive tolerance in male primates: Old paradigms and new evidence

Within social groups of primates, males commonly compete over reproduction, but they may also rely on cooperation with other males. Theory suggests that it may be adaptive for male primates to tolerate some reproduction by other males if reproductive tolerance fosters cooperation, particularly that dominant males yield so‐called reproductive concessions to subordinates to entice their cooperation. We review four recent studies that claimed to have found evidence for reproductive concessions or similar forms of reproductive tolerance. However, upon critical reevaluation of their results, no study provides conclusive support for reproductive concessions as predicted by theoretical models. Yet two studies demonstrated a form of reproductive tolerance that cannot be explained by any of the existing models, and that seems to have evolved only in multi‐male, multi‐female societies with diverse strategic options for males. Our article provides guidance how to study this form of reproductive tolerance in the absence of a unifying model.     

Epigenetic perspectives of safety in assisted reproductive technologies

To date, a wide range of assisted reproductive technologies is available for patients with impaired fertility. In general, the current methods of reproductive medicine are considered safe and do not significantly increase the frequency of birth of children with diseases or congenital malformations. However, the evidence has been accumulating in literature on higher risk of genomic imprinting diseases (Beckwith-Wiedemann and Angelman syndromes) as a result of using assisted reproductive technologies. In most cases examined, the appearance of these syndromes was explained by defective methylation status of imprinted genes. It has been suggested that manipulations with gametes and embryos during the period of total epigenetic modification of their genomes may act as potential risk factors of assisted reproductive technologies. Moreover, overcoming many natural reproductive barriers may contribute to the development of some pathological phenotypes. The review summarizes current views on epigenetic risk factors associated with assisted reproductive technologies.     

Reproductive Isolation during Domestication

It has been hypothesized that reproductive isolation should facilitate evolution under domestication. However, a systematic comparison of reproductive barrier strength between crops and their progenitors has not been conducted to test this hypothesis. Here, we present a systematic survey of reproductive barriers between 32 economically important crop species and their progenitors to better understand the role of reproductive isolation during the domestication process. We took a conservative approach, avoiding those types of reproductive isolation that are poorly known for these taxa (e.g., differences in flowering time). We show that the majority of crops surveyed are isolated from their progenitors by one or more reproductive barriers, despite the fact that the most important reproductive barrier in natural systems, geographical isolation, was absent, at least in the initial stages of domestication for most species. Thus, barriers to reproduction between crops and wild relatives are closely associated with domestication and may facilitate it, thereby raising the question whether reproductive isolation could be viewed as a long-overlooked "domestication trait." Some of the reproductive barriers observed (e.g., polyploidy and uniparental reproduction), however, may have been favored for reasons other than, or in addition to, their effects on gene flow.     

Temporal variation in reproductive costs and payoffs shapes the flowering strategy of a neotropical milkweed, <Emphasis Type="Italic">Asclepias curassavica</Emphasis>

A central goal of evolutionary ecology is to understand the factors that select for particular life history strategies, such as delaying reproduction. For example, environmental variation and reproductive costs to survival and growth often select for reproductive delays in semelparous and iteroparous species. In this study, we examine how variation in reproductive cost, which we define as a reduction to growth, survival, or future reproduction after a reproductive event, may select for reproductive delay in an iteroparous Neotropical milkweed with no obvious reproductive season. We analyzed demographic data collected every 3 months for 3 years from four populations of Asclepias curassavica in Monteverde, Costa Rica. We detected costs of flowering to survival and growth that varied in magnitude between our 12 transition periods without a seasonal pattern. The populations also exhibited temporal variation in reproductive payoffs measured as seedling establishment. We incorporated these reproductive costs into demographic projection models, which predicted a delayed flowering strategy only when we included temporal variation in costs and payoffs. Temporal variation in reproductive costs and payoffs is an important selective force in the evolution of delayed flowering in iteroparous species. Further, a lack of predictable seasonal pattern to reproductive costs and payoffs may contribute to the lack of seasonal reproductive patterns observed in our study species and other Neotropical species.     

Plasticity in resource allocation based life history traits in the Pacific oyster, Crassostrea gigas. I. Spatial variation in food abundance

We investigated the quantitative genetics of plasticity in resource allocation between survival, growth and reproductive effort in Crassostrea gigas when food abundance varies spatially. Resource allocation shifted from survival to growth and reproductive effort as food abundance increased. An optimality model suggests that this plastic shift may be adaptive. Reproductive effort plasticity and mean survival were highly heritable, whereas for growth, both mean and plasticity had low heritability. The genetic correlations between reproductive effort and both survival and growth were negative in poor treatments, suggesting trade-offs, but positive in rich ones. These sign reversals may reflect genetic variability in resource acquisition, which would only be expressed when food is abundant. Finally, we found positive genetic correlations between reproductive effort plasticity and both growth and survival means. The latter may reflect adaptation of C. gigas to differential sensitivity of fitness to survival, such that genetic variability in survival mean might support genetic variability in reproductive effort plasticity.     

Behavioural responses of female Neogobius melanostomus to odours of conspecifics

The behavioural responses of reproductive and non‐reproductive female round gobies Neogobius melanostomus to water conditioned by reproductive and non‐reproductive males and females were tested. The behavioural responses of reproductive female round gobies exposed to odour of reproductive males included increased time spent near the source of the odour, elevated swimming velocities and directed movement to and around the odour source when compared with their responses to control water. These results suggested that pheromones released from reproductive males may induce spawning behaviour in reproductive females. Non‐reproductive females exposed to reproductive female odour spent significantly more time near the odour source of reproductive females compared with control water. Non‐reproductive females also showed directed movement towards and around the odour source when exposed to reproductive female odour. These results suggested that round gobies use inter‐sexual and intra‐sexual pheromones and that both sex and reproductive status are important in the detection and release of these pheromones.     

Reproductive Asynchrony and the Divergence of Hawaiian Crickets

Asynchrony in reproductive behavior may contribute to reproductive isolation among sympatric species. While the 38 cryptic species of the genus Laupala are primarily distinguished on the basis of variation in pulse rate of male calling songs, additional phenotypes, such as asynchrony in reproductive behavior, may contribute to reproductive isolation in this genus. Here we document similarities and differences in the diel timing of two reproductive behaviors, male singing activity and insemination events. Asynchrony in the diel timing of male singing behavior was observed between two sympatric species, Laupala cerasina and Laupala paranigra, in the field. An interpopulational comparison within L. cerasina did not reveal variation in diel behavior patterns of singing between two locations. Asynchrony in the timing of copulation and sperm transfer between L. cerasina and L. paranigra was documented in the laboratory. The observed pattern of asynchrony in both the field and laboratory could have arisen in a number of ways. One possibility is that species diverged in sympatry because of interspecific interactions, producing a pattern of reproductive character displacement. Alternatively, the observed asynchrony in reproductive behavior may have played a role in the process of community assembly within this recently diverged cricket genus. The presence of interspecific variation and the absence of intraspecific variation revealed by our study do not support a pattern of reproductive character displacement for diel reproductive behavior, suggesting that the differences seen between species were not caused by recent species interactions.     

Reproductive effort reduces specific immune response and parasite resistance

If a trade-off exists between reproductive effort and immune function, life-history decisions may have important implications for parasite resistance. Here, we report effects of experimental manipulation of reproductive effort on subsequent specific immune function and parasite resistance in the collared flycatcher, Ficedula albicollis. Our results show that increased reproductive effort of females immunized with Newcastle disease virus (NDV) vaccine negatively affected the ability to respond with NDV-specific antibodies. We further show that increased reproductive effort increased the intensity of Haemoproteus infections and that such infections are associated with higher mortality. Our results thus provide support for the hypothesis that immune suppression caused by reproductive effort may be an important mechanism mediating the life-history cost of reproduction.     

Environmental Cues, Endocrine Factors, and Reproductive Diapause in Male Insects

Environmental cues, mostly photoperiod and temperature, mediated by effects on the neuroendocrine system, control reproductive diapause in female insects. Arrest of oocyte development characterizes female reproductive diapause, which has two major adaptive functions: It improves chances of survival during unfavorable season(s), and/or it confines oviposition to that period of the year that is optimal for survival of the eggs and progeny. Although reproductive diapause is less well studied in male insects, there may be no sex-dependent differences in regard to the first of these functions. The second one, however, is not valid for the male; instead, selection pressure directs the male's reproductive strategy toward maximum chances of fertilization of the female's eggs with minimum waste of energy. Therefore, in species with female reproductive diapause, the males may or may not exhibit diapause, but if they do, their diapause must be adapted to that existing in conspecific females. Male reproductive diapause is defined as a reversible state of inability of the male to inseminate receptive females. In relation to reproductive diapause, there are several patterns of coadaptations between male reproductive strategy and timing of female receptivity, (a) In some insects, the females are receptive in the early part of their diapause; mating occurs during this period and there is no diapause in the male. The male dies shortly after copulation and the female stores the sperms to fertilize the eggs that develop after termination of the female's diapause, (b) In some species, as in the grasshopper Anacridium aegyptium, females are receptive during diapause; though oocyte development is arrested, copulation occurs and the stored sperms fertilize the eggs when the female's diapause ends. Males were claimed to have no diapause, but recent studies have revealed the presence of a reproductive diapause in a proportion of the males. This and other cases show that female receptivity during reproductive diapause may or may not be accompanied by male reproductive diapause. If there is a reproductive diapause in the male, it is controlled by the same endocrine mechanism, the corpora allata (CA), as in the females, (c) In many species females are refractory during their diapause. In these cases, males exhibit reproductive diapause, which may be light, as in the beetle Oulema melanopus, or well established, as in certain grasshoppers, butterflies, and beetles. In the latter cases, male diapause is controlled by similar environmental cues (photoperiod, temperature) and by the same intrinsic mechanism (neuroendocrine system, especially CA) as female diapause. Nevertheless, male diapause is less intense; the environmental cues leading to its termination are less complex and/or less extreme, so male diapause terminates before that of the females. Presumably, male diapause is under two antagonistic selection pressures: A male should not waste energy by courting dia-pausing refractory females, but he should be ready to copulate as soon as the females become receptive, otherwise he may lose in the competition between males for females. Some further strategies, which do not seem to fit the above patterns, are also outlined.     

Decreased reproductive investment of female threespine stickleback Gasterosteus aculeatus infected with the cestode Schistocephalus solidus: parasite adaptation,host adaptation,or side effect?

Parasitic infections may cause alterations in host life history, including changes in reproductive investment (absolute amount of energy allocated to reproduction) and reproductive effort (proportion of available energy allocated to reproduction). Such changes in host life history may reflect: 1) a parasite tactic: the parasite adaptively manipulates energy flow within the host so that the host is induced to make a reduction in reproductive effort and reproductive investment, making more energy available to the parasite; 2) no tactic: there is no change in host reproductive effort and reproductive investment simply decreases as a side effect of the parasite depleting host energy stores; 3) a host tactic: the host adaptively increases reproductive effort in the face of infection and loss of body condition, reproductive investment possibly being reduced despite the increased reproductive effort. Females in Alaskan lake populations of threespine sticklebacks ( Gasterosteus aculeatus ) are capable of clutch production when parasitized by the cestode Schistocephalus solidus despite large relative parasite masses. We analyzed the somatic energy reserves, maturation stage and ovarian mass of female sticklebacks collected from an Alaska lake during a single reproductive season. We found that parasitized females were less likely to carry fully-matured gametes, had smaller ovarian masses, and had lower somatic energy stores than unparasitized females. The relationship between reproductive investment and energy storage did not differ between parasitized and unparasitized females. Thus, reproductive effort did not change in response to parasitic infection. We conclude there was no indication of either a parasite tactic or a host tactic. Simple nutrient theft is involved in the parasite's influence on host reproduction, consistent with an earlier hypothesis that reproductive curtailment in threespine sticklebacks is a side effect.