The Duration of Lactation in Antechinus-Stuartii (Marsupialia, Dasyuridae)

1992 ◽  
Vol 40 (2) ◽  
pp. 195 ◽  
Author(s):  
A Cockburn

Free-living Antechinus stuartii at the Monga State Forest showed almost no variation in date of birth, yet weaning took place over a period of three weeks. Males were weaned slightly earlier and at greater weights than females. When daughters were considered, weaning was delayed in years when breeding density was high, and females with ten teats weaned their young later and at slightly lower weights than females with eight teats. The difference between the two teat phenotypes was not simply associated with increased reproductive investment, as successful eight-teated mothers weaned their young earlier than less successful mothers, and there was no relation between weaning success and date of weaning for ten-teated mothers. Age of mother did not influence weaning weight or date, and mothers tended to wean at the same time in each year of their life. These patterns are discussed in relation to recent debate on the detection of life-history trade-offs in free-living populations.

2018 ◽  
Vol 285 (1892) ◽  
pp. 20182141 ◽  
Author(s):  
Stefania Casagrande ◽  
Michaela Hau

The trade-off between reproductive investment and survival is central to life-history theory, but the relative importance and the complex interactions among the physiological mechanisms mediating it are still debated. Here we experimentally tested whether baseline glucocorticoid hormones, the redox system or their interaction mediate reproductive investment–survival trade-offs in wild great tits ( Parus major ). We increased the workload of parental males by clipping three feathers on each wing, and 5 days later determined effects on baseline corticosterone concentrations (Cort), redox state (reactive oxygen metabolites, protein carbonyls, glutathione peroxidase [GPx], total non-enzymatic antioxidants), body mass, body condition, reproductive success and survival. Feather-clipping did not affect fledgling numbers, chick body condition, nest provisioning rates or survival compared with controls. However, feather-clipped males lost mass and increased both Cort and GPx concentrations. Within feather-clipped individuals, GPx increases were positively associated with reproductive investment (i.e. male nest provisioning). Furthermore, within all individuals, males that increased GPx suffered reduced survival rates. Baseline Cort increases were related to mass loss but not to redox state, nest provisioning or male survival. Our findings provide experimental evidence that changes in the redox system are associated with the trade-off between reproductive investment and survival, while baseline Cort may support this trade-off indirectly through a link with body condition. These results also emphasize that plastic changes in individuals, rather than static levels of physiological signals, may mediate life-history trade-offs.


2021 ◽  
pp. 1-11
Author(s):  
Gerlinde Höbel ◽  
Robb Kolodziej ◽  
Dustin Nelson ◽  
Christopher White

Abstract Information on how organisms allocate resources to reproduction is critical for understanding population dynamics. We collected clutch size (fecundity) and egg size data of female Eastern Gray Treefrogs, Hyla versicolor, and examined whether observed patterns of resource allocation are best explained by expectations arising from life history theory or by expected survival and growth benefits of breeding earlier. Female Hyla versicolor showed high between-individual variation in clutch and egg size. We did not observe maternal allocation trade-offs (size vs number; growth vs reproduction) predicted from life history theory, which we attribute to the large between-female variation in resource availability, and the low survival and post-maturity growth rate observed in the study population. Rather, clutches are larger at the beginning of the breeding season, and this variation in reproductive investment aligns with seasonal variation in ecological factors affecting offspring growth and survival.


2006 ◽  
Vol 63 (6) ◽  
pp. 995-1004 ◽  
Author(s):  
Gretta T. Pecl ◽  
Natalie A. Moltschaniwskyj

Abstract Many cephalopods continue growing while laying multiple egg batches over the adult life, with repro-somatic allocation continuing beyond attainment of reproductive maturity. Many species show extreme individual variation in reproductive investment. Factors driving this variation in adult Sepioteuthis australis were evaluated by examining allocation of energy to somatic and reproductive growth as a function of body shape, growth rate, maturation, and hatching season. Hatching season influence was sex-specific; males hatched in warmer months had greater reproductive investment, faster growth, and better somatic and reproductive condition, whereas females hatched in spring and summer had less reproductive investment. Seasonal impacts on life history resulted in an “alternation of generations”, with slow-growing squid in poor condition and with high levels of reproductive investment producing a generation with completely different life-history characteristics. This suggests that abiotic and biotic conditions that change seasonally could play a large role in determining energy allocated to reproduction. However, this was not driving trade-offs between size and number of offspring. Life-history trade-offs should be detectable as negative correlations between relevant traits. However, in Sepioteuthis australis there was little evidence of trade-offs between reproduction and growth or condition of individuals, suggesting a “live for today” lifestyle.


2010 ◽  
Vol 88 (9) ◽  
pp. 900-904
Author(s):  
F. Stephen Dobson ◽  
Pierre Jouventin

Williams (1966; Am. Nat. 100(916): 687–690) furthered R.A. Fisher’s concept of reproductive value by breaking it into two components: (1) current reproduction and (2) residual reproductive value (RRV, the summed product of survival and reproduction over the rest of the lifespan). He predicted a negative correlation of measures of these two components among species, and this prediction led in part to the idea of trade-offs in life-history theory. We tested Williams’ prediction with 24 species of albatrosses and petrels (order Procellariiformes), species with a great range of body sizes and all laying only one egg at a time (like humans, highly iteroparous). Two measures of reproductive investment were not negatively correlated with RRV. Adjusting data for body mass and phylogeny resulted in significant positive associations. In addition, any measure of annual parental allocation to reproduction (once adjusted for body size) should give a positive association with RRV as shown by a simple simulation model that assumes a highly iteroparous life cycle. Under such life cycles, Williams’ prediction confounds the positive influence of reproduction on both current investment and RRV. Principles of life-history theory, however, do not require re-evaluation, as this particular prediction can in at least some cases be internally inconsistent.


2021 ◽  
Author(s):  
Jean‐Louis Hemptinne ◽  
Emilie Lecompte ◽  
Arnaud Sentis ◽  
Anthony F. G. Dixon ◽  
Alexandra Magro

2019 ◽  
Author(s):  
Gretchen F. Wagner ◽  
Emeline Mourocq ◽  
Michael Griesser

Biparental care systems are a valuable model to examine conflict, cooperation, and coordination between unrelated individuals, as the product of the interactions between the parents influences the fitness of both individuals. A common experimental technique for testing coordinated responses to changes in the costs of parental care is to temporarily handicap one parent, inducing a higher cost of providing care. However, dissimilarity in experimental designs of these studies has hindered interspecific comparisons of the patterns of cost distribution between parents and offspring. Here we apply a comparative experimental approach by handicapping a parent at nests of five bird species using the same experimental treatment. In some species, a decrease in care by a handicapped parent was compensated by its partner, while in others the increased costs of care were shunted to the offspring. Parental responses to an increased cost of care primarily depended on the total duration of care that offspring require. However, life history pace (i.e., adult survival and fecundity) did not influence parental decisions when faced with a higher cost of caring. Our study highlights that a greater attention to intergenerational trade-offs is warranted, particularly in species with a large burden of parental care. Moreover, we demonstrate that parental care decisions may be weighed more against physiological workload constraints than against future prospects of reproduction, supporting evidence that avian species may devote comparable amounts of energy into survival, regardless of life history strategy.


2017 ◽  
Vol 49 (6) ◽  
pp. 783 ◽  
Author(s):  
Yan WANG ◽  
Zhenchao LIN ◽  
Bowen HOU ◽  
Shijin SUN

Author(s):  
Maren N. Vitousek ◽  
Laura A. Schoenle

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.


Sign in / Sign up

Export Citation Format

Share Document