Abstract

Summary 1 Life-history traits commonly associated with plant invasiveness are vegetative reproduction or r-selected traits such as short generation times and high rates of reproduction and individual growth. 2 We used matrix modelling to assess which demographic traits are important for the population growth of an invasive seaweed lacking vegetative reproduction and whether demographic and life-history strategies shift with increased dominance of the invader. The vital rates of one of the most successful invading seaweeds, Sargassum muticum, were investigated monthly for 2 years in intertidal pools dominated by the native brown seaweed Cystoseira humilis and by S. muticum, respectively. In order to speculate about the demographic mechanisms that determine invasiveness of S. muticum, and as the study sites were recently colonized, we assumed that C. humilis and S. muticum pools are proxies for early and late phases of invasion, respectively. 3 Both deterministic and stochastic matrix models showed positive rates of population growth, and rates were significantly higher in the pools dominated by S. muticum than in the ones dominated by C. humilis, indicating demographic changes with invader dominance. The variability of population growth rates and of reproductive and elasticity values of S. muticum was higher in the pools dominated by C. humilis, suggesting invader-driven stabilization of environmental conditions. Generation times of the species increased with invader dominance, supporting invader-stabilized environmental conditions. 4 Elasticity analyses revealed that the most important demographic trait for population growth rate at both levels of invader dominance was the persistence of the non-fertile adult fronds rather than reproduction or growth. No major shifts in the life-history strategy of S. muticum between levels of invader dominance were detected. 5 Synthesis. This study suggests that the invasiveness of S. muticum, a perennial invader without vegetative reproduction, relies on K- rather than r-selected traits and without drastic changes in life-history strategy between phases of invasion.

Highlights

  • The environmental and economic impacts of biological invasions are estimated to be USD 1.4 trillion per year or about 5% of the world economy (Pimentel 2002; IMF 2006)

  • We used matrix modelling to assess which demographic traits are important for the population growth of an invasive seaweed lacking vegetative reproduction and whether demographic and life-history strategies shift with increased dominance of the invader

  • The vital rates of one of the most successful invading seaweeds, Sargassum muticum, were investigated monthly for 2 years in intertidal pools dominated by the native brown seaweed Cystoseira humilis and by S. muticum, respectively

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Summary

Introduction

The environmental and economic impacts of biological invasions are estimated to be USD 1.4 trillion per year or about 5% of the world economy (Pimentel 2002; IMF 2006). Since the early works of Fisher (1937) and Baker (1965), invasion theory has attempted to identify which life-history traits best explain the successful establishment of invaders outside their native ranges. Traits examined include the ability to reproduce sexually and asexually, rate of growth from seedling to sexual maturity, phenotypic plasticity and high tolerance to environmental heterogeneity (Baker 1974). Santos variability of seed crop and have short juvenile periods (Kolar & Lodge 2001), others have essentially the same growth rates and fecundity as natives (Daehler 2003). Muth & Pigliucci (2006) did not detect phenology differences of introduced invasive species when compared to introduced non-invasives, in two closely related genera of Asteraceae. The ontogenetic development of an invasive Crepis or Centaurea was not faster than that of a non-invasive congener, neither size nor architecture was related to invasiveness

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