scholarly journals Life history evolution and phenotypic plasticity in parasitic eyebrights (Euphrasia, Orobanchaceae)

2018 ◽  
Author(s):  
Alex D. Twyford ◽  
Natacha Frachon ◽  
Edgar L. Y. Wong ◽  
Chris Metherell ◽  
Max R. Brown

ABSTRACTPremise of the studyParasite lifetime reproductive success is determined by both genetic variation and phenotypically plastic life history traits that respond to host quality and external environment. Here, we use the generalist parasitic plant genus Euphrasia to investigate life history trait variation, in particular whether there is a trade-off between growth and reproduction, and how life history traits are affected by host quality.MethodsWe perform a common garden experiment to evaluate life history trait differences between eleven Euphrasia taxa grown on a common host, document phenotypic plasticity when a single Euphrasia species is grown on eight different hosts, and relate our observations to trait differences recorded in the wild.Key resultsEuphrasia exhibit a range of life history strategies that differ between species that transition rapidly to flower at the expense of early season growth, and those that invest in vegetative growth and delay flowering. Many life history traits show extensive phenotypic plasticity in response to host quality and demonstrate the costs of attaching to a low-quality host.ConclusionsCommon garden experiments reveal trait differences between taxonomically complex Euphrasia species that are characterised by postglacial speciation and hybridisation. Our experiments suggest life history strategies in this generalist parasitic plant genus are the product of natural selection on traits related to growth and flowering. However, host quality may be a primary determinant of lifetime reproductive success.

2020 ◽  
Author(s):  
Vandana Revathi Venkateswaran ◽  
Olivia Roth ◽  
Chaitanya S. Gokhale

Males and females evolved distinct life-history strategies, reflected in diverse life-history traits, summarized as sexual dimorphism. Life-history traits are highly interlinked. The sex that allocates more resources towards offspring is expected to increase its life span, and this might require an efficient immune system. However, the other sex might allocate its resources towards ornamentation, and this might have immunosuppressive effects. Activity of immune response may not be specific to the sex that produces the eggs but could correlate with the amount of parental investment given. Informed by experimental data, we designed a theoretical framework that combines multiple life-history traits. We disentangled sex-biased life-history strategies from a particular sex to include species with reversed sex-roles, and male parental investment. We computed the lifetime reproductive success from the fitness components arising from diverse sex-biased life-history traits, and observed a strong bias in adult sex ratio depending on sex-specific resource allocation towards life-history traits. Overall, our work provides a generalized method to combine various life-history traits with sex-specific differences to calculate the lifetime reproductive success. This was used to explain certain empirical observations as a consequence of sexual dimorphism in life-history traits.


2018 ◽  
Vol 115 (17) ◽  
pp. 4441-4446 ◽  
Author(s):  
Mark R. Christie ◽  
Gordon G. McNickle ◽  
Rod A. French ◽  
Michael S. Blouin

The maintenance of diverse life history strategies within and among species remains a fundamental question in ecology and evolutionary biology. By using a near-complete 16-year pedigree of 12,579 winter-run steelhead (Oncorhynchus mykiss) from the Hood River, Oregon, we examined the continued maintenance of two life history traits: the number of lifetime spawning events (semelparous vs. iteroparous) and age at first spawning (2–5 years). We found that repeat-spawning fish had more than 2.5 times the lifetime reproductive success of single-spawning fish. However, first-time repeat-spawning fish had significantly lower reproductive success than single-spawning fish of the same age, suggesting that repeat-spawning fish forego early reproduction to devote additional energy to continued survival. For single-spawning fish, we also found evidence for a fitness trade-off for age at spawning: older, larger males had higher reproductive success than younger, smaller males. For females, in contrast, we found that 3-year-old fish had the highest mean lifetime reproductive success despite the observation that 4- and 5-year-old fish were both longer and heavier. This phenomenon was explained by negative frequency-dependent selection: as 4- and 5-year-old fish decreased in frequency on the spawning grounds, their lifetime reproductive success became greater than that of the 3-year-old fish. Using a combination of mathematical and individual-based models parameterized with our empirical estimates, we demonstrate that both fitness trade-offs and negative frequency-dependent selection observed in the empirical data can theoretically maintain the diverse life history strategies found in this population.


2020 ◽  
Vol 10 (1) ◽  
Author(s):  
Lisha L. Berzins ◽  
Russell D. Dawson ◽  
Christy A. Morrissey ◽  
Robert G. Clark

AbstractAnimal populations are influenced strongly by fluctuations in weather conditions, but long-term fitness costs are rarely explored, especially in short-lived avian species. We evaluated the relative contributions of individual characteristics and environmental conditions to lifetime reproductive success (LRS) of female tree swallows (Tachycineta bicolor) from two populations breeding in contrasting environments and geographies, Saskatchewan and British Columbia, Canada. Female swallows achieved higher LRS by breeding early in the season and producing more fledglings. Other measures of female quality had virtually no influence on LRS. Genetic factors did not predict LRS, as there was no correlation between life-history components for sister pairs nor between mothers and their daughters. Instead, climate variability—indexed by spring pond density (i.e., abundance of wetland basins holding water) during years when females bred—had strong positive effects on female LRS in more arid Saskatchewan but only weak positive effects of moisture conditions were detected in wetter British Columbia. Overall, several life history trait correlates of LRS were similar between populations, but local environmental factors experienced by individuals while breeding produced large differences in LRS. Consequently, variable and extreme environmental conditions associated with changing climate are predicted to influence individual fitness of distinct populations within a species’ range.


FACETS ◽  
2017 ◽  
Vol 2 (1) ◽  
pp. 34-52 ◽  
Author(s):  
Ashley Guncay ◽  
Thiropa Balasubramaniam ◽  
Katie Plagens ◽  
Joel Weadge ◽  
Tristan A.F. Long

In some species where males make no direct contribution to a female’s lifetime reproductive success, females choose mates based on the indirect benefits manifested in their offspring. One trait that may be subject to this sexual selection is immunocompetence (the ability to mount an immune response following exposure to pathogens); however, the results of previous work on its link to male attractiveness have been ambiguous. Herein we examine the life history consequences of mating with males with a history of failure or success in reproductive competitions in Drosophila melanogaster. By examining egg-to-adult survival, body weights, and bacterial loads of offspring reared in either the absence or presence of a bacterial pathogen, we were able to examine whether sire reproductive success was associated with their offsprings’ ability to respond to an immunological challenge and other life history traits. Our results are partially consistent with the predictions of the “immunocompetence handicap hypothesis”: competitively successful males (“studs”) sire male offspring that are better able to handle an immunological challenge than those sired by competitively unsuccessful males (“duds”). However, our assay also revealed the opposite pattern in female offspring, suggestive of the complicating presence of alleles with sexually antagonistic effects on the expression of this important life history trait.


2019 ◽  
Author(s):  
Jukka-Pekka Verta ◽  
Paul Vincent Debes ◽  
Nikolai Piavchenko ◽  
Annukka Ruokolainen ◽  
Outi Ovaskainen ◽  
...  

AbstractA major goal in biology is to understand how evolution shapes variation in individual life histories. Genome-wide association studies have been successful in uncovering genome regions linked with traits underlying life history variation in a range of species. However, lack of functional studies of the discovered genotype-phenotype associations severely restrains our understanding how alternative life history traits evolved and are mediated at the molecular level. Here, we report a cis-regulatory mechanism whereby expression of alternative isoforms of the transcription co-factor vestigial-like 3 (vgll3) associate with variation in a key life history trait, age at maturity, in Atlantic salmon (Salmo salar). Using a common-garden experiment, we first show that vgll3 genotype associates with puberty timing in one-year-old salmon males. By way of temporal sampling of vgll3 expression in ten tissues across the first year of salmon development, we identify a pubertal transition in vgll3 expression where maturation coincided with a 66% reduction in testicular vgll3 expression. The late maturation allele was not only associated with a tendency to delay puberty, but also with expression of a rare transcript isoform of vgll3 pre-puberty. By comparing absolute vgll3 mRNA copies in heterozygotes we show that the expression difference between the early and late maturity alleles is largely cis-regulatory. We propose a model whereby expression of a rare isoform from the late allele shifts the liability of its carriers towards delaying puberty. These results reveal how regulatory differences can be a central mechanism for the evolution of life history traits.Author summaryAlternative life history strategies are an important source of diversity within populations and promote the maintenance of adaptive capacity and population resilience. However, in many cases the molecular basis of different life history strategies remains elusive. Age at maturity is a key adaptive life history trait in Atlantic salmon and has a relatively simple genetic basis. Using salmon age at maturity as a model, we report a mechanism whereby different transcript isoforms of the key age at maturity gene, vestigial-like 3 (vgll3), associate with variation in the timing of male puberty. Our results show how gene regulatory differences in conjunction with variation in gene transcript structure can encode for complex alternative life histories.


2021 ◽  
Author(s):  
Anik Dutta ◽  
Fanny E. Hartmann ◽  
Carolina Sardinha Francisco ◽  
Bruce A. McDonald ◽  
Daniel Croll

AbstractThe adaptive potential of pathogens in novel or heterogeneous environments underpins the risk of disease epidemics. Antagonistic pleiotropy or differential resource allocation among life-history traits can constrain pathogen adaptation. However, we lack understanding of how the genetic architecture of individual traits can generate trade-offs. Here, we report a large-scale study based on 145 global strains of the fungal wheat pathogen Zymoseptoria tritici from four continents. We measured 50 life-history traits, including virulence and reproduction on 12 different wheat hosts and growth responses to several abiotic stressors. To elucidate the genetic basis of adaptation, we used genome-wide association mapping coupled with genetic correlation analyses. We show that most traits are governed by polygenic architectures and are highly heritable suggesting that adaptation proceeds mainly through allele frequency shifts at many loci. We identified negative genetic correlations among traits related to host colonization and survival in stressful environments. Such genetic constraints indicate that pleiotropic effects could limit the pathogen’s ability to cause host damage. In contrast, adaptation to abiotic stress factors was likely facilitated by synergistic pleiotropy. Our study illustrates how comprehensive mapping of life-history trait architectures across diverse environments allows to predict evolutionary trajectories of pathogens confronted with environmental perturbations.


Author(s):  
Gaotian Zhang ◽  
Jake D Mostad ◽  
Erik C Andersen

Abstract Life history traits underlie the fitness of organisms and are under strong natural selection. A new mutation that positively impacts a life history trait will likely increase in frequency and become fixed in a population (e.g. a selective sweep). The identification of the beneficial alleles that underlie selective sweeps provides insights into the mechanisms that occurred during the evolution of a species. In the global population of Caenorhabditis elegans, we previously identified selective sweeps that have drastically reduced chromosomal-scale genetic diversity in the species. Here, we measured the fecundity of 121 wild C. elegans strains, including many recently isolated divergent strains from the Hawaiian islands and found that strains with larger swept genomic regions have significantly higher fecundity than strains without evidence of the recent selective sweeps. We used genome-wide association (GWA) mapping to identify three quantitative trait loci (QTL) underlying the fecundity variation. Additionally, we mapped previous fecundity data from wild C. elegans strains and C. elegans recombinant inbred advanced intercross lines that were grown in various conditions and detected eight QTL using GWA and linkage mappings. These QTL show the genetic complexity of fecundity across this species. Moreover, the haplotype structure in each GWA QTL region revealed correlations with recent selective sweeps in the C. elegans population. North American and European strains had significantly higher fecundity than most strains from Hawaii, a hypothesized origin of the C. elegans species, suggesting that beneficial alleles that caused increased fecundity could underlie the selective sweeps during the worldwide expansion of C. elegans.


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