The Growth Rate Hypothesis as a predictive framework for microevolutionary adaptation to selection for high population growth: an experimental test under phosphorus rich and phosphorus poor conditions

The growth rate hypothesis, a central concept of Ecological Stoichiometry, explains the frequently observed positive association between somatic growth rate and somatic phosphorus content (Psom) in organisms across a broad range of taxa. Here, we explore its potential in predicting intraspecific microevolutionary adaptation. For this, we subjected zooplankton populations to selection for fast population growth (PGR) in either a P-rich (HP) or P-poor (LP) food environment. With common garden transplant experiments we demonstrate evolution in HP populations towards increased PGR concomitant with an increase in Psom. In contrast we show that LP populations evolved higher PGR independently of Psom. We conclude that the GRH hypothesis has considerable value for predicting microevolutionary change, but that its application may be contingent on stoichiometric context. Our results highlight the potential of cryptic evolution in determining the performance response of field populations to elemental limitation of their food resources.

Size evolution in microorganisms masks trade-offs predicted by the growth rate hypothesis

Adaptation to local resource availability depends on responses in growth rate and nutrient acquisition. The growth rate hypothesis (GRH) suggests that growing fast should impair competitive abilities for phosphorus and nitrogen due to high demand for biosynthesis. However, in microorganisms, size influences both growth and uptake rates, which may mask trade-offs and instead generate a positive relationship between these traits (size hypothesis, SH). Here, we evolved a gradient of maximum growth rate ( μ max ) from a single bacterium ancestor to test the relationship among μ max , competitive ability for nutrients and cell size, while controlling for evolutionary history. We found a strong positive correlation between μ max and competitive ability for phosphorus, associated with a trade-off between μ max and cell size: strains selected for high μ max were smaller and better competitors for phosphorus. Our results strongly support the SH, while the trade-offs expected under GRH were not apparent. Beyond plasticity, unicellular populations can respond rapidly to selection pressure through joint evolution of their size and maximum growth rate. Our study stresses that physiological links between these traits tightly shape the evolution of competitive strategies.