Cost of Reproduction and Female Life-History Tactics in a Population of Grass Snakes, Natrix natrix, in Southern Sweden

Oikos ◽  
1987 ◽  
Vol 49 (2) ◽  
pp. 129 ◽  
Author(s):  
Thomas Madsen
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.


2012 ◽  
Vol 179 (5) ◽  
pp. E147-E162 ◽  
Author(s):  
Emilie Macke ◽  
Sara Magalhães ◽  
Hong Do-Thi Khanh ◽  
Adrien Frantz ◽  
Benoît Facon ◽  
...  

2007 ◽  
Vol 18 (3) ◽  
pp. 551-555 ◽  
Author(s):  
Alexei A. Maklakov ◽  
Natacha Kremer ◽  
Göran Arnqvist

2007 ◽  
Vol 3 (6) ◽  
pp. 674-677 ◽  
Author(s):  
G Proaktor ◽  
E.J Milner-Gulland ◽  
T Coulson

The shape of the association between age and the cost of reproduction varies across species. However, it is unclear whether there are any general patterns in the way the cost of reproduction varies with life history, taxon or ecological function. Using a simple theoretical method, we identified three characteristic patterns to describe the age-related survival cost of reproduction. The most frequent pattern is an approximately exponential decay (ED) with increasing age. Two additional u-shaped patterns were identified, where the cost of reproduction was higher for young and old individuals compared with intermediate-aged individuals. The majority of these u-shaped curves suggested higher costs of reproduction at older ages (RQ), with the rest suggesting a higher cost at young ages (LQ). While predators were most likely to exhibit ED-shaped cost curves, herbivores were equally likely to exhibit ED and RQ curves; birds were likely to exhibit ED-shaped curves and mammals were split equally between ED and RQ curves. These findings suggest that there may be predictable differences in the age-related shape of the cost of reproduction between species, but further research is required to identify the mechanisms generating such differences.


2009 ◽  
Vol 5 (3) ◽  
pp. 339-342 ◽  
Author(s):  
Gregory E. Blomquist

Trade-offs are central to life-history theory but difficult to document. Patterns of phenotypic and genetic correlations in rhesus macaques, Macaca mulatta —a long-lived, slow-reproducing primate—are used to test for a trade-off between female age of first reproduction and adult survival. A strong positive genetic correlation indicates that female macaques suffer reduced adult survival when they mature relatively early and implies primate senescence can be explained, in part, by antagonistic pleiotropy. Contrasts with a similar human study implicate the extension of parental effects to later ages as a potential mechanism for circumventing female life-history trade-offs in human evolution.


Evolution ◽  
2020 ◽  
Vol 74 (2) ◽  
pp. 365-376 ◽  
Author(s):  
David C. S. Filice ◽  
Rajat Bhargava ◽  
Reuven Dukas

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