scholarly journals Predator-Induced Plasticity on Warning Signal and Larval Life-History Traits of the Aposematic Wood Tiger Moth, Arctia plantaginis

2021 ◽  
Vol 9 ◽  
Author(s):  
Diana Abondano Almeida ◽  
Johanna Mappes ◽  
Swanne Gordon
Keyword(s):  
Life History ◽  
Predation Risk ◽  
Life Histories ◽  
Development Time ◽  
Life History Traits ◽  
Environmental Changes ◽  
Warning Signal ◽  
Black Body ◽  
Tiger Moth ◽  
Tiger Moths

Predator-induced plasticity in life-history and antipredator traits during the larval period has been extensively studied in organisms with complex life-histories. However, it is unclear whether different levels of predation could induce warning signals in aposematic organisms. Here, we investigated whether predator-simulated handling affects warning coloration and life-history traits in the aposematic wood tiger moth larva, Arctia plantaginis. As juveniles, a larger orange patch on an otherwise black body signifies a more efficient warning signal against predators but this comes at the costs of conspicuousness and thermoregulation. Given this, one would expect that an increase in predation risk would induce flexible expression of the orange patch. Prior research in this system points to plastic effects being important as a response to environmental changes for life history traits, but we had yet to assess whether this was the case for predation risk, a key driver of this species evolution. Using a full-sib rearing design, in which individuals were reared in the presence and absence of a non-lethal simulated bird attack, we evaluated flexible responses of warning signal size (number of orange segments), growth, molting events, and development time in wood tiger moths. All measured traits except development time showed a significant response to predation. Larvae from the predation treatment developed a more melanized warning signal (smaller orange patch), reached a smaller body size, and molted more often. Our results suggest plasticity is indeed important in aposematic organisms, but in this case may be complicated by the trade-off between costly pigmentation and other life-history traits.

scholarly journals The life-history basis of behavioural innovations

2016 ◽  
Vol 371 (1690) ◽  
pp. 20150187 ◽  
Author(s):  
Daniel Sol ◽  
Ferran Sayol ◽  
Simon Ducatez ◽  
Louis Lefebvre
Keyword(s):  
Life History ◽  
Life Histories ◽  
Life History Traits ◽  
Environmental Changes ◽  
Adaptive System ◽  
Brain Size ◽  
Life History Strategy ◽  
Evolutionary Origin ◽  
Generalist Species ◽  
Previous Evidence

The evolutionary origin of innovativeness remains puzzling because innovating means responding to novel or unusual problems and hence is unlikely to be selected by itself. A plausible alternative is considering innovativeness as a co-opted product of traits that have evolved for other functions yet together predispose individuals to solve problems by adopting novel behaviours. However, this raises the question of why these adaptations should evolve together in an animal. Here, we develop the argument that the adaptations enabling animals to innovate evolve together because they are jointly part of a life-history strategy for coping with environmental changes. In support of this claim, we present comparative evidence showing that in birds, (i) innovative propensity is linked to life histories that prioritize future over current reproduction, (ii) the link is in part explained by differences in brain size, and (iii) innovative propensity and life-history traits may evolve together in generalist species that frequently expose themselves to novel or unusual conditions. Combined with previous evidence, these findings suggest that innovativeness is not a specialized adaptation but more likely part of a broader general adaptive system to cope with changes in the environment.

Hormones and Behavior

2019 ◽  
pp. 11-26
Author(s):  
Maren N. Vitousek ◽  
Laura A. Schoenle
Keyword(s):  
Life History ◽  
Life Histories ◽  
Life History Traits ◽  
Developmental Plasticity ◽  
Endocrine System ◽  
Phenotypic Traits ◽  
Social Environments ◽  
Trade Offs ◽  
And Behavior

Hormones mediate the expression of life history traits—phenotypic traits that contribute to lifetime fitness (i.e., reproductive timing, growth rate, number and size of offspring). The endocrine system shapes phenotype by organizing tissues during developmental periods and by activating changes in behavior, physiology, and morphology in response to varying physical and social environments. Because hormones can simultaneously regulate many traits (hormonal pleiotropy), they are important mediators of life history trade-offs among growth, reproduction, and survival. This chapter reviews the role of hormones in shaping life histories with an emphasis on developmental plasticity and reversible flexibility in endocrine and life history traits. It also discusses the advantages of studying hormone–behavior interactions from an evolutionary perspective. Recent research in evolutionary endocrinology has provided insight into the heritability of endocrine traits, how selection on hormone systems may influence the evolution of life histories, and the role of hormonal pleiotropy in driving or constraining evolution.

A Primer of Life Histories

2021 ◽  
Author(s):  
Jeffrey A. Hutchings
Keyword(s):  
Life History ◽  
Life Histories ◽  
Life History Theory ◽  
Life History Traits ◽  
Reproductive Effort ◽  
Effective Means ◽  
Academic Experience ◽  
Sustainable Exploitation ◽  
Evolution Of Life ◽  
Opportune Time

Life histories describe how genotypes schedule their reproductive effort throughout life in response to factors that affect their survival and fecundity. Life histories are solutions that selection has produced to solve the problem of how to persist in a given environment. These solutions differ tremendously within and among species. Some organisms mature within months of attaining life, others within decades; some produce few, large offspring as opposed to numerous, small offspring; some reproduce many times throughout their lives while others die after reproducing just once. The exponential pace of life-history research provides an opportune time to engage and re-engage new generations of students and researchers on the fundamentals and applications of life-history theory. Chapters 1 through 4 describe the fundamentals of life-history theory. Chapters 5 through 8 focus on the evolution of life-history traits. Chapters 9 and 10 summarize how life-history theory and prediction has been applied within the contexts of conservation and sustainable exploitation. This primer offers an effective means of rendering the topic accessible to readers from a broad range of academic experience and research expertise.

scholarly journals Density Dependence, Evolutionary Optimization, and the Diversification of Avian Life Histories

The Condor ◽  
2000 ◽  
Vol 102 (1) ◽  
pp. 9-22 ◽  
Author(s):  
Robert E. Ricklefs
Keyword(s):  
Life History ◽  
Life Table ◽  
Life Histories ◽  
Life History Traits ◽  
Evolutionary Ecology ◽  
Reproductive Rate ◽  
Empirical Modeling ◽  
Adult Survival ◽  
Life History Variation ◽  
Evolutionary Response

Abstract Although we have learned much about avian life histories during the 50 years since the seminal publications of David Lack, Alexander Skutch, and Reginald Moreau, we still do not have adequate explanations for some of the basic patterns of variation in life-history traits among birds. In part, this reflects two consequences of the predominance of evolutionary ecology thinking during the past three decades. First, by blurring the distinction between life-history traits and life-table variables, we have tended to divorce life histories from their environmental context, which forms the link between the life history and the life table. Second, by emphasizing constrained evolutionary responses to selective factors, we have set aside alternative explanations for observed correlations among life-history traits and life-table variables. Density-dependent feedback and independent evolutionary response to correlated aspects of the environment also may link traits through different mechanisms. Additionally, in some cases we have failed to evaluate quantitatively ideas that are compelling qualitatively, ignored or explained away relevant empirical data, and neglected logical implications of certain compelling ideas. Comparative analysis of avian life histories shows that species are distributed along a dominant slow-fast axis. Furthermore, among birds, annual reproductive rate and adult mortality are directly proportional to each other, requiring that pre-reproductive survival is approximately constant. This further implies that age at maturity increases dramatically with increasing adult survival rate. The significance of these correlations is obscure, particularly because survival and reproductive rates at each age include the effects of many life-history traits. For example, reproductive rate is determined by clutch size, nesting success, season length, and nest-cycle length, each of which represents the outcome of many different interactions of an individual's life-history traits with its environment. Resolution of the most basic issues raised by patterns of life histories clearly will require innovative empirical, modeling, and experimental approaches. However, the most fundamental change required at this time is a broadening of the evolutionary ecology paradigm to include a variety of alternative mechanisms for generating patterns of life-history variation.

Life histories of North American game birds: a reanalysis

1988 ◽  
Vol 66 (8) ◽  
pp. 1906-1912 ◽  
Author(s):  
Todd W. Arnold
Keyword(s):  
Life History ◽  
North American ◽  
Life Histories ◽  
Life History Traits ◽  
Reproductive Effort ◽  
Cost Of Reproduction ◽  
Reproductive Value ◽  
Trade Offs ◽  
Game Birds ◽  
The Cost

Recently, Zammuto (R. M. Zammuto. 1986. Can. J. Zool. 64: 2739–2749) suggested that North American game birds exhibited survival–fecundity trade-offs consistent with the "cost of reproduction" hypothesis. However, there were four serious problems with the data and the analyses that Zammuto used: (i) the species chosen for analysis ("game birds") showed little taxonomic or ecological uniformity, (ii) the measures of future reproductive value (maximum longevity) were severely biased by unequal sample sizes of band recoveries, (iii) the measures of current reproductive effort (clutch sizes) were inappropriate given that most of the birds analyzed produce self-feeding precocial offspring, and (iv) the statistical units used in the majority of analyses (species) were not statistically independent with respect to higher level taxonomy. After correcting these problems, I found little evidence of survival–fecundity trade-offs among precocial game birds, and I attribute most of the explainable variation in life-history traits of these birds to allometry, phylogeny, and geography.

Life history variation in plants: an exploration of the fast-slow continuum hypothesis

1996 ◽  
Vol 351 (1345) ◽  
pp. 1341-1348 ◽  
Keyword(s):  
Life History ◽  
Life Histories ◽  
Sexual Maturity ◽  
Life History Traits ◽  
Continuum Hypothesis ◽  
Adult Mortality ◽  
Life Cycles ◽  
Differential Mortality ◽  
Life History Variation ◽  
Net Reproductive Rate

Several empirical models have attempted to account for the covariation among life history traits observed in a variety of organisms. One of these models, the fast-slow continuum hypothesis, emphasizes the role played by mortality at different stages of the life cycle in shaping the large array of life history variation. Under this scheme, species can be arranged from those suffering high adult mortality levels to those undergoing relatively low adult mortality. This differential mortality is responsible for the evolution of contrasting life histories on either end of the continuum. Species undergoing high adult mortality are expected to have shorter life cycles, faster development rates and higher fecundity than those experiencing lower adult mortality. The theory has proved accurate in describing the evolution of life histories in several animal groups but has previously not been tested in plants. Here we test this theory using demographic information for 83 species of perennial plants. In accordance with the fast-slow continuum, plants undergoing high adult mortality have shorter lifespans and reach sexual maturity at an earlier age. However, demographic traits related to reproduction (the intrinsic rate of natural increase, the net reproductive rate and the average rate of decrease in the intensity of natural selection on fecundity) do not show the covariation expected with longevity, age at first reproducion and life expectancy at sexual maturity. Contrary to the situation in animals, plants with multiple meristems continuously increase their size and, consequently, their fecundity and reproductive value. This may balance the negative effect of mortality on fitness, thus having no apparent effect in the sign of the covariation between these two goups of life history traits.

Coevolutionary interactions between host life histories and parasite life cycles

Parasitology ◽  
1998 ◽  
Vol 116 (S1) ◽  
pp. S47-S55 ◽  
Author(s):  
J. C. Koella ◽  
P. Agnew ◽  
Y. Michalakis
Keyword(s):  
Life History ◽  
Life Cycle ◽  
Life Histories ◽  
Life History Traits ◽  
Evolutionary Ecology ◽  
Life Cycles ◽  
Microsporidian Parasite ◽  
History Of ◽  
Host Life ◽  
Host Parasite

SummarySeveral recent studies have discussed the interaction of host life-history traits and parasite life cycles. It has been observed that the life-history of a host often changes after infection by a parasite. In some cases, changes of host life-history traits reduce the costs of parasitism and can be interpreted as a form of resistance against the parasite. In other cases, changes of host life-history traits increase the parasite's transmission and can be interpreted as manipulation by the parasite. Alternatively, changes of host's life-history traits can also induce responses in the parasite's life cycle traits. After a brief review of recent studies, we treat in more detail the interaction between the microsporidian parasite Edhazardia aedis and its host, the mosquito Aedes aegypti. We consider the interactions between the host's life-history and parasite's life cycle that help shape the evolutionary ecology of their relationship. In particular, these interactions determine whether the parasite is benign and transmits vertically or is virulent and transmits horizontally.Key words: host-parasite interaction, life-history, life cycle, coevolution.

scholarly journals Insulin-like growth factor-1 is associated with life-history variation across Mammalia

2014 ◽  
Vol 281 (1782) ◽  
pp. 20132458 ◽  
Author(s):  
Eli M. Swanson ◽  
Ben Dantzer
Keyword(s):  
Life History ◽  
Growth Factor ◽  
Life Histories ◽  
Life History Traits ◽  
Mammalian Species ◽  
Insulin Like Growth Factor ◽  
Life History Variation ◽  
Time Period ◽  
Path Analyses ◽  
Size Growth

Despite the diversity of mammalian life histories, persistent patterns of covariation have been identified, such as the ‘fast–slow’ axis of life-history covariation. Smaller species generally exhibit ‘faster’ life histories, developing and reproducing rapidly, but dying young. Hormonal mechanisms with pleiotropic effects may mediate such broad patterns of life-history variation. Insulin-like growth factor 1 (IGF-1) is one such mechanism because heightened IGF-1 activity is related to traits associated with faster life histories, such as increased growth and reproduction, but decreased lifespan. Using comparative methods, we show that among 41 mammalian species, increased plasma IGF-1 concentrations are associated with fast life histories and altricial reproductive patterns. Interspecific path analyses show that the effects of IGF-1 on these broad patterns of life-history variation are through its direct effects on some individual life-history traits (adult body size, growth rate, basal metabolic rate) and through its indirect effects on the remaining life-history traits. Our results suggest that the role of IGF-1 as a mechanism mediating life-history variation is conserved over the evolutionary time period defining mammalian diversification, that hormone–trait linkages can evolve as a unit, and that suites of life-history traits could be adjusted in response to selection through changes in plasma IGF-1.

Life-history traits of a small-bodied coastal shark

2013 ◽  
Vol 64 (1) ◽  
pp. 54 ◽  
Author(s):  
Adrian N. Gutteridge ◽  
Charlie Huveneers ◽  
Lindsay J. Marshall ◽  
Ian R. Tibbetts ◽  
Mike B. Bennett
Keyword(s):  
Life History ◽  
Life Histories ◽  
Life History Traits ◽  
Logistic Function ◽  
Early Maturation ◽  
Large Size ◽  
History Of ◽  
Age Model ◽  
Best Fit ◽  
Combined Data

The life histories of small-bodied coastal sharks, particularly carcharhinids, are generally less conservative than those of large-bodied species. The present study investigated the life history of the small-bodied slit-eye shark, Loxodon macrorhinus, from subtropical Hervey Bay, Queensland, and compared this species' biology to that of other coastal carcharhinids. The best-fit age model provided parameters of L∞ = 895 mm total length (TL), k = 0.18 and t0 = –6.3 for females, and L∞ = 832 mm TL, k = 0.44 and t0 = –2.6 for males. For sex-combined data, a logistic function provided the best fit, with L∞ = 842 mm TL, k = 0.41 and α = –2.2. Length and age at which 50% of the population was mature was 680 mm TL and 1.4 years for females, and 733 mm TL and 1.9 years for males. Within Hervey Bay, L. macrorhinus exhibited an annual seasonal reproductive cycle, producing an average litter of 1.9 ± 0.3 s.d. With the exception of the low fecundity and large size at birth relative to maximum maternal TL, the life-history traits of L. macrorhinus are comparable to other small-bodied coastal carcharhinids, and its apparent fast growth and early maturation contrasts that of large-bodied carcharhinids.

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