Variation in the reproductive rate of bats

2004 ◽  
Vol 82 (5) ◽  
pp. 688-693 ◽  
Author(s):  
Robert M.R Barclay ◽  
Joel Ulmer ◽  
Cameron J.A MacKenzie ◽  
Megan S Thompson ◽  
Leif Olson ◽  
...  
Keyword(s):  
Life History ◽  
Life Histories ◽  
Life History Theory ◽  
Life History Traits ◽  
Prey Availability ◽  
Weather Conditions ◽  
Reproductive Rate ◽  
Tropical Species ◽  
Allocation Of Resources ◽  
Reproductive Rates

In many respects, bats have relatively slow life histories. However, the reproductive rate of bats (i.e., the proportion of females that reproduce in any breeding season) has not been critically examined. We compiled data on the reproductive rates of bats to test predictions based on life-history theory. Among 257 samples from 103 species, reproductive rate varied considerably and was typically under 100%. Temperate-zone species had significantly lower and more variable reproductive rates than did tropical species. Reproductive rate also varied among families, with species in the Vespertilionidae having particularly high rates. As predicted based on life-history theory, reproductive rate was negatively correlated with longevity, and among vespertilionids, species with larger litters had higher reproductive rates. Thus, the data suggest that bats have relatively slow reproductive rates and, as in other life-history traits, fall at the "slow" end of the fast–slow life-history continuum found among mammals. Female bats, especially those in temperate regions, appear to adjust their allocation of resources to reproduction, and at times forego reproduction, perhaps in relation to their body condition, prey availability, and weather conditions.

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.

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.

Sexual size dimorphism and life history traits in an island-mainland system: an overview of the lizard genus Microlophus

2021 ◽  
pp. 1-7
Author(s):  
Ken S. Toyama ◽  
Christopher K. Boccia
Keyword(s):  
Life History ◽  
South America ◽  
Life History Theory ◽  
Life History Traits ◽  
Sexual Size Dimorphism ◽  
Life History Strategies ◽  
Galápagos Islands ◽  
Size Dimorphism ◽  
Rensch's Rule ◽  
Comprehensive Compilation

Abstract Opposing life history strategies are a common result of the different ecological settings experienced by insular and continental species. Here we present a comprehensive compilation of data on sexual size dimorphism (SSD) and life history traits of Microlophus, a genus of lizards distributed in western South America and the Galápagos Islands, and test for differences between insular and continental species under life history theory expectations. Contrary to our predictions, we found no differences in SSD between localities or evidence that Microlophus follows Rensch’s rule. However, as expected, head dimensions and maturity sizes were significantly larger in insular species while continental species had larger clutches. Our results show that Microlophus exhibits some of the patterns expected from an island-mainland system, but unexplained patterns will only be resolved through future ecological, morphological and behavioural studies integrating both faunas.

scholarly journals Life history and habitat do not mediate temporal changes in body size due to climate warming in rodents

PeerJ ◽  
2020 ◽  
Vol 8 ◽  
pp. e9792
Author(s):  
Aluwani Nengovhela ◽  
Christiane Denys ◽  
Peter J. Taylor
Keyword(s):  
Life History ◽  
Body Size ◽  
Climate Warming ◽  
Life History Traits ◽  
Vegetation Type ◽  
Reproductive Rate ◽  
Temporal Changes ◽  
Temporal Response ◽  
Extrinsic Factors ◽  
African Species

Temporal changes in body size have been documented in a number of vertebrate species, with different contested drivers being suggested to explain these changes. Among these are climate warming, resource availability, competition, predation risk, human population density, island effects and others. Both life history traits (intrinsic factors such as lifespan and reproductive rate) and habitat (extrinsic factors such as vegetation type, latitude and elevation) are expected to mediate the existence of a significant temporal response of body size to climate warming but neither have been widely investigated. Using examples of rodents, we predicted that both life history traits and habitat might explain the probability of temporal response using two tests of this hypothesis. Firstly, taking advantage of new data from museum collections spanning the last 106 years, we investigated geographical and temporal variation in cranial size (a proxy for body size) in six African rodent species of two murid subfamilies (Murinae and Gerbillinae) of varying life history, degree of commensality, range size, and habitat. Two species, the commensal Mastomys natalensis, and the non-commensal Otomys unisulcatus showed significant temporal changes in body size, with the former increasing and the latter decreasing, in relation with climate warming. Commensalism could explain the increase in size with time due to steadily increasing food availability through increased agricultural production. Apart from this, we found no general life history or habitat predictors of a temporal response in African rodents. Secondly, in order to further test this hypothesis, we incorporated our data into a meta-analysis based on published literature on temporal responses in rodents, resulting in a combined dataset for 50 species from seven families worldwide; among these, 29 species showed no significant change, eight showed a significant increase in size, and 13 showed a decline in size. Using a binomial logistic regression model for these metadata, we found that none of our chosen life history or habitat predictors could significantly explain the probability of a temporal response to climate warming, reinforcing our conclusion based on the more detailed data from the six African species.

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.

Dimensionless numbers and the assembly rules for life histories

1991 ◽  
Vol 332 (1262) ◽  
pp. 41-48 ◽  
Keyword(s):  
Life History ◽  
Life Histories ◽  
Life History Theory ◽  
Assembly Rules ◽  
Dimensionless Numbers ◽  
Age Of Maturity

This paper reviews recent efforts to use certain dimensionless numbers (DLNs) to classify life histories in plants and animals. These DLNs summarize the relation between growth, mortality and maturation, and several groups of animals show interesting patterns with respect to their numeric values. Finally we focus on one DLN, the product of the age of maturity and the adult instantaneous mortality, to show how evolutionary life history theory may be used to predict the value of the DLN, which differs greatly between major groups of animals.

scholarly journals Corticosterone, testosterone and life-history strategies of birds

2010 ◽  
Vol 277 (1697) ◽  
pp. 3203-3212 ◽  
Author(s):  
Michaela Hau ◽  
Robert E. Ricklefs ◽  
Martin Wikelski ◽  
Kelly A. Lee ◽  
Jeffrey D. Brawn
Keyword(s):  
Life History ◽  
Body Mass ◽  
Breeding Season ◽  
Life History Traits ◽  
Survival Rates ◽  
Life History Strategies ◽  
Adult Survival ◽  
Tropical Species ◽  
Published Data ◽  
Season Length

Steroid hormones have similar functions across vertebrates, but circulating concentrations can vary dramatically among species. We examined the hypothesis that variation in titres of corticosterone (Cort) and testosterone (T) is related to life-history traits of avian species. We predicted that Cort would reach higher levels under stress in species with higher annual adult survival rates since Cort is thought to promote physiological and behavioural responses that reduce risk to the individual. Conversely, we predicted that peak T during the breeding season would be higher in short-lived species with high mating effort as this hormone is known to promote male fecundity traits. We quantified circulating hormone concentrations and key life-history traits (annual adult survival rate, breeding season length, body mass) in males of free-living bird species during the breeding season at a temperate site (northern USA) and a tropical site (central Panama). We analysed our original data by themselves, and also combined with published data on passerine birds to enhance sample size. In both approaches, variation in baseline Cort (Cort0) among species was inversely related to breeding season length and body mass. Stress-induced corticosterone (MaxCort) also varied inversely with body mass and, as predicted, also varied positively with annual adult survival rates. Furthermore, species from drier and colder environments exhibited lower MaxCort than mesic and tropical species; T was lowest in species from tropical environments. These findings suggest that Cort0, MaxCort and T modulate key vertebrate life-history responses to the environment, with Cort0 supporting energetically demanding processes, MaxCort promoting survival and T being related to mating success.

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.

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