1988
DOI: 10.2307/1941251
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Sexual Differences in Biomass and Nutrient Allocation in the Dioecious Rubus Chamaemorus

Abstract: I compared the seasonal pattern of biomass distribution and amounts of N and P in male and female ramets of the dioecious perennial herb Rubus chamaemorus L. Two populations, one in an open and one in a shaded habitat, were studied for 2 yr. The cost offruit production in terms of reduction in vegetative growth was estimated in a field experiment.Ramets were larger, but the proportions of aboveground biomass, N, and P that were allocated to reproduction were lower at the shaded site than at the open site. The … Show more

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Cited by 173 publications
(138 citation statements)
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“…23). Indeed, clonality might more strongly trade-off against investment in female sex function than male sex function (27,39). If this is generally true and trade-offs between clonal growth and pollen production are usually weak, we predict that this should have two contrasting effects on the fitness of clones via their pollen production.…”
Section: Discussionmentioning
confidence: 90%
“…23). Indeed, clonality might more strongly trade-off against investment in female sex function than male sex function (27,39). If this is generally true and trade-offs between clonal growth and pollen production are usually weak, we predict that this should have two contrasting effects on the fitness of clones via their pollen production.…”
Section: Discussionmentioning
confidence: 90%
“…The foliar N/P mass ratio is a well-documented indicator of nutrient limitation to the growth of wild species: plant growth would be N-limited at N/P ratios < 14, P-limited at N/P ratios > 16, and co-limited by N and P at intermediate values [12]. By comparison, the N/P ratio in cloudberry leaves was in the range of 12 to 14 in Sweden [15], and of 7 to 11 in Scotland [14] and Norway [16,17].…”
Section: Introductionmentioning
confidence: 99%
“…In this way, it is necessary to consider the temporary variation to improve our estimation of the edge effects on the reproduction of studied species. For example, although we could not currently detect a bias between sexes, which, by the way, may depend on several factors as differences between male and female plants in the age or size to the sexual maturity, or differences in the flowering frequency between plants of different sexes (Meagher 1980), to long term, bias in sexual rates between edge and interior of fragments may be expected, because in contrast with male plants, survival rates of female plants can be decreased in stressed environments as consequence of a less resources allocation to the survival and a high allocation to the reproduction (e.g., Agren 1988, Gehring & Linhart 1993, Yu & Lu 2011. Additionally, it is important to consider other factors that can influence juvenile densities in the edge and the interior of the fragments.…”
Section: Discussionmentioning
confidence: 99%