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26 results for “differential allocation”
Data from: Separating differential allocation by females from direct effects of male condition in a beetle
<p>Differential allocation is the adjustment of reproductive allocation, typically by a female, in response to the quality of her male partner. A recent theoretical model suggests that differential allocation may influence trade-offs between reproductive traits within a breeding attempt. Furthermore, it is often difficult to distinguish differential allocation from direct effects of male condition. We address these gaps using a novel cross-fostering design to exclude direct effects of male condition and to test whether differential allocation affects trade-offs between and within breeding attempts. This design detects differential allocation as effects of a female's mating partner and direct effects of male condition as effects of the larvae's sire. We used the burying beetle Nicrophorus vespilloides, a species which adjusts reproductive allocation by culling some larvae after hatching. We used food-deprivation to manipulate the nutritional condition of both the female's mating partner and the larvae's sire. We find clear evidence for differential allocation as females mating with food-deprived males had fewer larvae than females mating with control males. There was a trade-off between number and size of larvae when females mated with control males, but a positive relationship when females mated with food-deprived males. Thus, differential allocation influenced relationships between reproductive traits within a breeding attempt, but not necessarily through trade-offs. Instead, we suggest that there may be cryptic heterogeneity in quality among females or their mating partners that was only exposed when females mated with a male in poor condition.</p>
Data from: Can females differentially allocate resources to offspring sired by different males?
<p>The viviparity-driven conflict hypothesis postulates that the evolution of matrotrophy (postfertilization maternal provisioning) will result in a shift from a pre- to postcopulatory mate choice and thus accelerate the evolution of postcopulatory reproductive isolation. Here, we perform artificial insemination experiments on <em>Heterandria formosa</em>, a matrotrophic poeciliid fish, to probe for evidence of postcopulatory female choice. We established laboratory populations from Wacissa River (WR) and Lake Jackson (LJ). The WR females normally produce larger offspring than the LJ females. We artificially inseminated females with sperm from each population or from both populations simultaneously. When LJ females were inseminated with sperm from WR and LJ males, they allocated fewer resources to WR-sired offspring than when they were inseminated with WR sperm alone. The LJ females carrying developing offspring sired by males from different populations were thus able to discriminate against non-resident males when allocating resources to developing young. The WR females, which normally produce larger offspring than LJ females, did not discriminate among males from different localities. These findings provide insights into the ability of females from one population to exercise a form of postcopulatory mate selection.</p>
Differential sex allocation strategies between females and facultative hermaphrodites of Chamaelirium hisauchianum (Melanthiaceae)
<p><span>Species of <em>Chamaelirium</em> are known to be highly diversified in sexual characters, but there has been no detailed empirical approach to elucidate the mechanism and process of sexual diversification in the genus. This paper reports the results of population-based analyses on various sexual aspects of <em>C. hisauchianum</em> endemic to Japan. Of the 20 populations surveyed, eight (40%) were composed of facultative hermaphrodites highly labile in sexual expression, exhibiting a wide range of gradational variation from hermaphroditism through andromonoecy to male. The remaining 12 populations (60 %) consisted of females and facultative hermaphrodites. In them, 11.8–30.9% (mean 22.2%) of the individuals were female. With no reciprocal sex changes, females and facultative hermaphrodites were regarded as, plausibly genetically determined, discrete sex morphs. In contrast, sexual expression in both sex morphs appeared resource dependent. Besides the difference in floral sexual traits, the average ratio of ovuliferous flowers in females was higher than that in facultative hermaphrodites. The production of ovuliferous flowers by females was less susceptible to both field and cultivated conditions and tended to be significantly relatively higher under unfavorable growing conditions. Females were thus less plastic (or more persistent) in producing ovuliferous flowers (or female organs) than facultative hermaphrodites irrespective of internal and external conditions. In all populations, andromonoecious plants dominated (50.8–100%), which appeared to reflect the high plasticity in sex allocation of facultative hermaphrodites. The different modes of sex allocation were regarded as secondary sex characters and presumably stem from a difference in easiness or attainability of sexual reproduction between the two sex morphs. </span></p>
Differential sex allocation strategies between females and facultative hermaphrodites of Chamaelirium hisauchianum (Melanthiaceae)
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Data from: Separating differential allocation by females from direct effects of male condition in a beetle
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Data from: Can females differentially allocate resources to offspring sired by different males?
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Data from: Forecasting the future? Differential allocation of maternal hormones in function of experimentally manipulated social contexts in blue tits Cyanistes caeruleus
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Data from: Importance of whole-plant biomass allocation and reproductive timing to habitat differentiation across the North American sunflowers
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Data from: Context-dependence of maternal effects: testing assumptions of optimal egg size, differential- and sex-allocation models
If offspring develop in adverse conditions, the maternal component of their phenotypic variation might increase due to the stronger dependence of offspring traits on parental investment. This should result in increased parental investment to individual offspring, as assumed by the model of optimal egg size. The opposite pattern, i.e., stronger dependence of offspring fitness on parental investment and consequently larger parental investment under good conditions is assumed by both the theory of differential allocation if attractive males provide material benefits, and reproductive compensation if they invest less into paternal care. Another influential idea is the Trivers-Willard model, which assumes sex-specific dependence of offspring fitness on parental investment. Here we tested these ideas by examining the effects of egg size on offspring fitness across many postnatal contexts in the Collared Flycatcher Ficedula albicollis. We employed a cross-fostering design that generated variation in egg size within nests and used brood means of fledgling mass as a functional measure of the quality of rearing conditions. Effects of egg size on three offspring traits, including lifetime reproductive success of recruits, were more pronounced in low-quality broods. These results support the assumption of the model of optimal egg size. Based on female preference for males providing material benefits, this pattern could support differential allocation, if attractive males invest less in paternal care, or reproductive compensation, if they invest more. By comparison, we did not find any evidence for sex specificity of fitness returns that might explain sex monomorphism of egg size in this species. The challenge for future studies will be the integration of components of parental investment and offspring fitness into their global measures and testing how the former affects the latter across gradients of postnatal conditions.
Female differential allocation in response to extra-pair offspring and social mate attractiveness
<p>Renewed debate over what benefits females might gain from producing extra-pair offspring emphasizes the possibility that apparent differences in quality between within-pair and extra-pair offspring are confounded by greater maternal investment in extra-pair offspring. Moreover, the attractiveness of a female's social mate can also influence contributions of both partners to a reproductive attempt. Here we explore the complexities involved in parental investment decisions in response to extra-pair offspring and mate attractiveness with a focus on the female point of view. Adult zebra finches paired and reproduced in a colony setting. A male's early-life diet quality and his extra-pair reproductive success were used as metrics of his mating attractiveness. Females paired with males that achieved extra-pair success laid heavier eggs than other females and spent less time attending their nests than their mates or other females. Extra-pair nestlings were fed more protein-rich hen's egg than within-pair nestlings. Females producing extra-pair offspring had more surviving sons than females producing only within-pair offspring. Collectively, results show that females differentially allocate resources in response to offspring extra-pair status and their social mate's attractiveness. Females may also obtain fitness benefits through the production of extra-pair offspring.</p>
Plant neighbors differentially alter a focal species' biotic interactions through changes to resource allocation
<p>Plant resource allocation strategies are thought to be largely a consequence of changing abiotic conditions and evolutionary history. However, biotic interactions also influence how a plant allocates resources. As a result, plants mediate indirect interactions between organisms above- and belowground through resource allocation. Neighboring plants can influence plant fitness directly through competition for resources, and indirectly by altering associated community interactions (associational effects). Given the importance of community interactions for plant success, and the known ability for plant neighbors to change these interactions, the goal of this "pandemic project" was to separate inter- and intraspecific plant associations, above- and belowground, to understand how different plant neighbors alter plant resource allocation, and if this in turn alters biotic interactions. We specifically investigated associational effects on herbivory and soil microbial community interactions. To do so, we established a common garden experiment, manipulating plant neighbors and extent of interactions (aboveground only versus above- and belowground interactions, using customized pot types), and measured changes to a focal plant and its biotic interactions over two growing seasons. We found evidence of both neighbor effects and pot type, showing that neighbor interactions affect a focal plant through both above- and belowground processes, and how the focal plant is affected depends on neighbor identity. Though neighbors did not directly alter herbivory or most soil microbial interactions, they did alter the relationship between belowground microbial communities and plant function. Resource allocation responses were reduced with time, showing the importance of extending experiments beyond a single growing season, and is an important consideration when making predictions about plant responses to changing conditions. This study contributes to a growing body of work showing how the community context affects the above- and belowground interactions of a plant through plant resource allocation strategies.</p>
Plant neighbors differentially alter a focal species’ biotic interactions through changes to resource allocation
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Data from: Allocation to male vs. female floral function varies by currency and responds differentially to density and moisture stress
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Female differential allocation in response to extra-pair offspring and social mate attractiveness
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Data from: Context-dependence of maternal effects: testing assumptions of optimal egg size, differential- and sex-allocation models
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Data from: Differential allocation in a lekking bird: females lay larger eggs and are more likely to have male chicks when they mate with less related males
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Data from: Differential allocation revisited: when should mate quality affect parental investment?
Differential allocation (DA) is the adaptive adjustment of reproductive investment (up or down) according to partner quality. A lack of theoretical treatments has led to some confusion in the interpretation of DA in the empirical literature. We present a formal framework for DA that highlights the nature of reproductive benefits versus costs for females mated to males of different quality. Contrary to popular belief, analytical and stochastic dynamic models both show that additive benefits of male quality on offspring fitness have no effect on optimal levels of female investment and thus cannot produce DA. Instead, if offspring fitness is affected multiplicatively by male quality, or male quality affects the female cost function, DA is expected because of changes in the marginal benefits or costs of extra investment. Additive male quality effects on the female cost function can cause a novel form of weak DA, because reduced costs can slightly favor current over future reproduction. Combinations of these distinct effects in more realistic model scenarios can explain various patterns of positive and negative DA reported for different species and mating systems. Our model therefore sheds new light on the diversity of empirical results by providing a strong conceptual framework for the differential allocation hypothesis.
Figure 3 from: Ting JJ, Judge KA, Gwynne DT (2017) Listening to male song induces female field crickets to differentially allocate reproductive resources. Journal of Orthoptera Research 26: 205-210. https://doi.org/10.3897/jor.26.19891
Figure 3 - Mean (±SE) size of embryos laid during: the first week following treatment (Week 1), and the subsequent weeks following treatment (Post Week 1) of females who experienced either low- (grey symbols) or high- (black symbols) quality calling song.
Figure 2 from: Ting JJ, Judge KA, Gwynne DT (2017) Listening to male song induces female field crickets to differentially allocate reproductive resources. Journal of Orthoptera Research 26: 205-210. https://doi.org/10.3897/jor.26.19891
Figure 2 - Mean (±SE) change in mass during: the first week following treatment (Week 1), and the subsequent weeks following treatment (Post Week 1) of females who experienced either low- (grey symbols) or high- (black symbols) quality calling song.
Figure 1 from: Ting JJ, Judge KA, Gwynne DT (2017) Listening to male song induces female field crickets to differentially allocate reproductive resources. Journal of Orthoptera Research 26: 205-210. https://doi.org/10.3897/jor.26.19891
Figure 1 - Mean (±SE) latency of females to choose the speaker broadcasting either low- or high-quality calling song.
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