Search results for "Cost of reproduction"

COST OF REPRODUCTION IN THE WILD: MANIPULATION OF REPRODUCTIVE EFFORT IN THE BANK VOLE

2003

For three years, we manipulated litter size by adding or subtracting pups in eight wild populations of the bank vole, Clethrionomys glareolus, to examine reproductive costs and allocation of reproductive effort between offspring number and size. In general, litter enlargements did not increase the number of weanlings per mother and significantly decreased the size of weanlings. Reproductive effort and the breeding success of individuals varied within breeding seasons, but time of breeding and litter manipulation did not interact to affect reproductive trade-offs. Our 3-yr field experiment revealed that litter enlargements also reduced survival and fecundity of mothers. Small mammals have be…

Cost of reproduction in Callosobruchus maculatus: effects of mating on male longevity and the effect of male mating status on female longevity.

2005

One of the most studied life-history trade-offs is that resulting from the cost of reproduction: a trade-off arises when reproduction diverts limited resources from other life-history traits. We examine the cost of reproduction in male, and the effect of male mating status on female Callosobruchus maculatus seed beetles. Cost of reproduction for male C. maculatus was manifested as reduced longevity. There was also a positive relationship between male body size and male longevity. Females mated to males that had already copulated twice did not live as long as females mated to males that had copulated once or not at all. The third copulation of males also lasted longer than the two previous o…

When the seasons don't fit: Speedy molt as a routine carry-over cost of reproduction

2013

The failure of animals to fit all life-cycle stages into an annual cycle could reduce the chances of successful breeding. In some cases, non-optimal strategies will be adopted in order to maintain the life-cycle within the scope of one year. We studied trade-offs made by a High Arctic migrant shorebird, the red knot Calidris canutus islandica, between reproduction and wing feather molt carried out in the non-breeding period in the Dutch Wadden Sea. We compared primary molt duration between birds undertaking the full migratory and breeding schedule with birds that forego breeding because they are young or are maintained in captivity. Molt duration was ca. 71 days in breeding adults, which wa…

Increased susceptibility to oxidative stress as a proximate cost of reproduction

2004

Maternal investment in relation to sex ratio and offspring number in a small mammal – a case for Trivers and Willard theory?

2009

1. Optimal parental sex allocation depends on the balance between the costs of investing into sons vs. daughters and the benefits calculated as fitness returns. The outcome of this equation varies with the life history of the species, as well as the state of the individual and the quality of the environment. 2. We studied maternal allocation and subsequent fecundity costs of bank voles, Myodes glareolus, by manipulating both the postnatal sex ratio (all-male/all-female litters) and the quality of rearing environment (through manipulation of litter size by -2/+2 pups) of their offspring in a laboratory setting. 3. We found that mothers clearly biased their allocation to female rather than ma…

Bilateral Monopoly: A Contribution by Francesco Ferrara

2009

In this paper, we propose an interpretation of the application of "cost of reproduction" of Francesco Ferrara to the exchange between two agents to highlight its relevance for the theory of bilateral monopoly. In the Teoria delle Mercedi (1863), Ferrara gives a numerical example to explain price determination in the exchange between one buyer and one seller. Here, this example is translated into a mathematical model that reproduces the fundamental issues of the neoclassical debate on the indeterminacy of price in the Cournot model (1938), and anticipates the solutions proposed by Edgeworth (1881) at the end of this debate.

Data from: The oxidative cost of reproduction depends on early development oxidative stress and sex in a bird species

2016

In the early 2000’s, a new component of the cost of reproduction was proposed: oxidative stress. Since then the oxidative cost of reproduction hypothesis has, however, received mixed support. Different arguments have been provided to explain this. Among them, the lack of a life history perspective on most experimental tests was suggested. We manipulated the levels of a key intracellular antioxidant (glutathione) in captive zebra finches (Taeniopygia guttata) during a short period of early life and subsequently tested the oxidative cost of reproduction. Birds were allowed to mate freely in an outdoor aviary during several months. We repeatedly enlarged or reduced their broods to increase or …