Male Life History, Reproductive Effort, and the Evolution of the Genus Homo

2012 ◽  
Vol 53 (S6) ◽  
pp. S424-S435 ◽  
Author(s):  
Richard G. Bribiescas ◽  
Peter T. Ellison ◽  
Peter B. Gray
2006 ◽  
Vol 84 (1) ◽  
pp. 143-150 ◽  
Author(s):  
Stephen P. Bonser ◽  
Lonnie W. Aarssen

Generalisations of life histories in plants are often framed in terms of allocation to reproduction. For example, relative allocation to reproduction is commonly found to be higher in semelparous than in iteroparous plant species. However, the association between vegetative traits and life history has been largely unexplored. In higher plants, reproductive and vegetative function can be measured in terms of meristem allocation. Under this approach, two vegetative traits (apical dominance (the suppression of axillary meristem development) and branching intensity (the commitment of axillary meristems to branches)) can be measured as well as one reproductive trait (reproductive effort). We used phylogenetically independent contrasts to compare reproductive and vegetative function in annual semelparous and perennial iteroparous species. Twenty congeneric species pairs (each species pair represented by one semelparous and one iteroparous species) across nine families were selected based on availability of herbarium specimens. Semelparous life-history evolution was associated with higher reproductive effort. Conversely, iteroparous life-history evolution was associated with higher apical dominance. Branching intensity was not associated with life history. An evolutionary association between life history and apical dominance but not branching intensity suggests a complex relationship between allocation to vegetative traits and the evolution of plant strategies across environments.


Author(s):  
Jeffrey A. Hutchings

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.


1985 ◽  
Vol 63 (5) ◽  
pp. 938-945 ◽  
Author(s):  
Patricia S. Muir ◽  
James E. Lotan

Mature serotinous and nonserotinous trees of Pinus contorta Dougl. var. latifolia Engelm. in the Bitterroot Watershed of western Montana do not differ in most life-history characteristics (reproductive or vegetative). No differences between trees of the two cone types were found in height, basal area, basal area growth rates over the lives of the trees, or crown ratio. Cone number, weights of individual cones and seeds, and estimates of reproductive effort were similar in serotinous and non-serotinous trees. Reproductive characteristics were either independent of tree age, or related similarly in trees of the two cone types. Nonserotinous trees may, however, have more seeds per cone than serotinous trees. This difference in seed numbers may be adaptive if serotinous trees invest relatively heavily in cone materials to protect seeds (which are retained in cones for many years), while nonserotinous trees (which shed seeds each year) invest relatively heavily in seeds. Trees of the two cone types differ mainly in the particular types of disturbance favoring their regeneration, but they often grow in the same stands where there are similar selective pressures on most aspects of their biology. Gene flow between them probably homogenizes all but those differences maintained by strong selective pressures.


1988 ◽  
Vol 66 (8) ◽  
pp. 1906-1912 ◽  
Author(s):  
Todd W. Arnold

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.


1995 ◽  
Vol 65 (1) ◽  
pp. 41-52 ◽  
Author(s):  
Kimberly A. Hughes

SummaryThis paper describes the results of assays of male life-history characters in a large outbred laboratory population of D. melanogaster. Lines of flies homozygous for the entire third chromosome and lines of flies carrying two different third chromosomes were assayed for agespecific male mating ability (MMA), age-specific survivorship, male fertility, and body mass. The results of these assays were used to calculate the inbreeding decline associated with each of these traits, the average dominance of deleterious alleles that affect the traits, the genotypic and environmental components of variance for the homozygous lines, and phenotypic and genotypic correlations among the characters. Significant inbreeding decline was found for all characters except the Gompertz intercept and fertility. Early and late MMA show larger effects of inbreeding than any other trait. The inbreeding load for MMA is about the same magnitude as that for egg-to-adult viability, but is substantially less than that associated with total fitness. The estimated inbreeding decline and average dominance of male life-history characters are comparable to estimates for other Drosophila fitness components.


1990 ◽  
Vol 68 (1) ◽  
pp. 44-48 ◽  
Author(s):  
Larry D. Marshall

Daily egg production of the moth Parapediasia teterrella declined over the life-span of the female but egg size remained constant. The absence of water resulted in lower fecundity and early mortality. Egg size and lifetime fecundity showed considerable inter-individual variation and large females produced more and larger eggs than their smaller counterparts. Large females expended greater reproductive effort than small females. Hatching success was negatively related to egg size. In spite of this, large females laying large eggs had higher fitness than small females. I postulate that multiple reproductive strategies within a species, resulting from differences in reproductive effort expended, may explain why expected trade-offs in reproductive parameters (e.g., egg size versus egg number) were not found in this species. Furthermore, I argue that the prevalent interpretation of life-history evolution (that body size is the important determining parameter of life-history parameters) may reflect correlation of body size with reproductive effort, and reproductive effort may be more important in determining the nature of trade-offs between reproductive parameters.


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