Dioecious plant populations have generally been considered to maintain sex ratios of 1:1 (Allen & Antos 1993, Carroll & Mulcahy 1993, Charnov 1982). The sex ratio does, however, change if the plants are growing in a stressful environment, often being male-biased under these conditions (Ortiz et al. 1998, 2002). This pattern has been explained by differences in how the sexes resolve their respective energy requirements (Obeso et al. 1998). Females generally assign more resources to reproduction in comparison to growth and maintenance than do males, and they are smaller and longer-lived (Allen & Antos 1993, Nicotra 1999, Obeso et al. 1998, Willson 1983). Thus their higher reproductive costs take a toll on females, modifying the population sex ratio in favour of males (Allen & Antos 1993, Lovett-Doust & Lovett-Doust 1988). However, in order to determine the reproductive cost it is necessary to consider the compensatory mechanisms (Obeso 2002). These reduce the reproductive cost and include plastic response in terms of plant architecture and plant physiology. For example, nutrient resorption is a process that may help decrease dependence on nutrient intake, thereby constituting an important nutrient economy mechanism that can also reduce the reproductive cost if a significant proportion of the nutrients had been reassigned to reproduction (Killingbeck 1986, Obeso 2002).