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Biology subjects

Burd, M.

Publications and source records attributed to Burd, M..

2 recordsLinked to original sources

The concept of the gain curve

Gain curves were introduced to explain how hermaphrodites could displace a dioecious population, and to account for sexual allocation in hermaphrodites. Terms for gamete production employed for the first purpose were transformed for the second into male and female gain curves that ostensibly defined fitness outcomes. These gain curves pose a conceptual challenge if they are specified separately because fitness at the population level cannot occur through one sex function independently of success through the other. If gain curves truly represent fitness outcomes, anomalies can arise, such as inequality of total male and female fitness in a population. Gain curves were originally used in a mathematical framework that treated the ostensible gain functions as inputs of male and female actors to a mating arena rather than as mating outcomes from that arena. I present a model of sex allocation that incorporates power functions to describe both gamete production and fitness gain in a manner that explicitly separates these two roles. In this formulation, the gamete production functions have the identical effect on optimal sex allocation originally attributed to gain curves while the true fitness gain curves lose nearly all effect on the optimum. Thus, despite the label, gain curves were implicitly describing inputs rather than outcomes. Because gain curves have been a staple of evolutionary ecology for decades, the implication is that much of our understanding of sexual allocation in hermaphrodites needs to be revisited. I outline some directions such an effort might take.

evolutionary biology↗

Australian native flower colours: does nectar reward drive bee pollinator flower preferences?

Colour is an important signal that flowering plants use to attract insect pollinators like bees. Previous research in Germany has shown that nectar volume is higher for flower colours that are innately preferred by European bees, suggesting an important link between colour signals, bee preferences and floral rewards. In Australia, flower colour signals have evolved in parallel to the Northern hemisphere to enable easy discrimination and detection by the phylogenetically ancient trichromatic visual system of bees, and native Australian bees also possess similar innate colour preferences to European bees. We measured 59 spectral signatures from flowers present at two preserved native habitats in South Eastern Australia and tested whether there were any significant differences in the frequency of flowers presenting higher nectar rewards depending upon the colour category of the flower signals, as perceived by bees. We also tested if there was a significant correlation between chromatic contrast and the frequency of flowers presenting higher nectar rewards. For the entire sample, and for subsets excluding species in the Asteraceae and Orchidaceae, we found no significant difference among colour categories in the frequency of high nectar reward. This suggests that whilst such relationships between flower colour signals and nectar volume rewards have been observed at a field site in Germany, the effect is likely to be specific at a community level rather than a broad general principle that has resulted in the common signalling of bee flower colours around the world.

ecology↗