Extremely low fecundity and highly female-biased sex ratio in nest-living spider mite Schizotetranychus brevisetosus (Acari: Tetranychidae)

2017 ◽  
Vol 22 (2) ◽  
pp. 170 ◽  
Author(s):  
Kaori Tamura ◽  
Katsura Ito
Keyword(s):  
Life History ◽  
Sex Ratio ◽  
Life Histories ◽  
Life History Traits ◽  
Defense Mechanism ◽  
Intrinsic Rate ◽  
Spider Mites ◽  
Natural Increase ◽  
Blue Oak ◽  
Life Type

Spider mites show various life types characterized by spinning behavior, web structure, and sociality. Individuals of the woven-nest (WN) species construct silken nests on the undersurface of host leaves, inside which they develop and reproduce. This nesting behavior may be related with the defense mechanism and life history traits of mites in the stable habitat (e.g., evergreen trees). If the WN life type affects the life-history traits, these traits may be similar within WN species. The WN species are known to be fragmentarily distributed in diverse genera, Stigmaeopsis, Schizotetranychus, Eotetranychus, and Oligonychus, and their life types are suspected to have secondarily converged. However, their life histories have not been elucidated except for several species in specific genera. To supply the information in Schizotetranychus, we investigated the demographic traits and the sex ratio of Schizotetranychus brevisetosus, which shows the WN life type and lives on the evergreen Japanese blue oak Quercus glauca. We estimated the development time of females as 22.6 ± 3.1 days (mean ± SD, n = 22) and the fecundity of fertilized females as 13.7 ± 5.9 (n = 37) at 25°C. The sex ratio of males to the total number of adults at emergence was low (0.072). The intrinsic rate of natural increase (rm) was estimated as 0.060 day-1, one of the lowest ever reported for spider mites at the same temperature. The present results were similar to other WN species in that fecundity and male ratio were low. 

Life history and feeding biology of the predatory thrips, Aleurodothrips fasciapennis (Thysanoptera: Phlaeothripidae)

1998 ◽  
Vol 88 (3) ◽  
pp. 351-357 ◽  
Author(s):  
D.M. Watson ◽  
T.Y. Du ◽  
M. Li ◽  
J.J. Xiong ◽  
D.G. Liu ◽  
...  
Keyword(s):  
Life History ◽  
Relative Humidity ◽  
Sex Ratio ◽  
Intrinsic Rate ◽  
Natural Increase ◽  
Adult Longevity ◽  
Female Fecundity ◽  
Adult Sex Ratio ◽  
Survival And Reproduction ◽  
Low Humidity

AbstractDetails of the life history, the effects of relative humidity and temperature on survival and reproduction, and the predatory ability of Aleurodothrips fasciapennis Franklin were examined under laboratory conditions. Stage-specific development and adult longevity were similar between sexes, and the adult sex ratio was 1:1. Females laid 23.3 ± 18.0 eggs of which 83% hatched. The survival rate of first instars to adulthood was 82%. The intrinsic rate of natural increase (rm) was 0.04, assuming a zero or 5.4 day pre-oviposition interval. Temperature did not affect the proportion of eggs that hatched, the proportion of first instars surviving to adulthood or adult sex ratios. However, female fecundity was dependent on temperature being highest at 24 ndash 28°C. Relative humidity did not affect adult sex ratio or female fecundity but the proportion of eggs hatched and the survival of first instars to adulthood increased as relative humidity increased. Few eggs hatched when relative humidity was <65%. Larval and adult female A. fasciapennis were voracious feeders but the number of prey killed per progeny was high, suggesting A. fasciapennis was inefficient at converting prey into progeny biomass. The potential value of A. fasciapennis as a biocontrol agent of Aonidiella aurantii (Maskell) on Australian citrus is discussed in terms of its rm, prey killing power and environmental adaptability. It is concluded that population growth of A. fasciapennis should exceed that of A. aurantii under field conditions but A. fasciapennis may be of little value against A. aurantii on citrus grown under conditions of high temperature and low humidity, or when prey densities are low.

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.

Critique of some practices in life-history studies, with special reference to harpacticoid copepods

1984 ◽  
Vol 35 (3) ◽  
pp. 375 ◽  
Author(s):  
M Bergmans
Keyword(s):  
Life History ◽  
Reproductive Strategies ◽  
Life Histories ◽  
Ad Hoc ◽  
Intrinsic Rate ◽  
Intrinsic Rate Of Increase ◽  
Conceptual Level ◽  
Cognitive Framework ◽  
Rate Of Increase ◽  
Harpacticoid Copepods

Published studies on the demography and reproductive strategies of harpacticoid copepods are examined critically. At the technical level, the popular approximation r ≈ In R0/Tc is shown to be inappropriate as an estimate of the intrinsic rate of increase of harpacticoids. It leads to a systematic underestimation, by 8-29%, for life histories typical of fast-breeding species. Various ad hoc variants of r and R0 calculations occurring in the literature are also criticized. .At the conceptual level, a more discriminating approach to life-history characteristics is necessary; this applies both to the assessment of their 'strategic' significance, and to their diagnostic power with regard to the various 'strategies'. Special attention is given to the non-equivalence of parity and voltinism. Recommendations that should promote the construction of a more rigorous cognitive framework are included.

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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