Photic niche invasions: phylogenetic history of the dim-light foraging augochlorine bees (Halictidae)

• Published in: Proceedings of the Royal Society. B, Biological sciences Biological sciences, 2012-02, Vol.279 (1729), p.794-803
• Main Authors: Tierney, Simon M, Sanjur, Oris, Grajales, Grethel G, Santos, Leandro M, Bermingham, Eldredge, Wcislo, William T
• Format: Article
• Language: English
• Subjects: Adaptation, Physiological; Adaptive Radiation; amino acids; Animals; Apoidea; Augochlorini; Bayes Theorem; Bees; Bees - genetics; Bees - physiology; Behavior, Animal; Biological Evolution; Bumblebees; chemical structure; Circadian Rhythm; codons; Dim-Light; DNA; DNA - chemistry; Evolution; Foraging; Fossils; Halictidae; Honey bees; Insect behavior; Insect genetics; Light; Magnoliophyta; Materials; Megalopta; mutation; Opsin; Opsins; Photic Stimulation; Phylogenetics; Phylogeny; Relictual Taxa; vision
• ISSN: 0962-8452; 1471-2954; 1471-2945
• DOI: 10.1098/rspb.2011.1355

Most bees rely on flowering plants and hence are diurnal foragers. From this ancestral state, dim-light foraging in bees requires significant adaptations to a new photic environment. We used DNA sequences to evaluate the phylogenetic history of the most diverse clade of Apoidea that is adapted to dim-light environments (Augochlorini: Megalopta, Megaloptidia and Megommation). The most speciose lineage, Megalopta, is distal to the remaining dim-light genera, and its closest diurnal relative (Xenochlora) is recovered as a lineage that has secondarily reverted to diurnal foraging. Tests for adaptive protein evolution indicate that long-wavelength opsin shows strong evidence of stabilizing selection, with no more than five codons (2%) under positive selection, depending on analytical procedure. In the branch leading to Megalopta, the amino acid of the single positively selected codon is conserved among ancestral Halictidae examined, and is homologous to codons known to influence molecular structure at the chromophore-binding pocket. Theoretically, such mutations can shift photopigment λmax sensitivity and enable visual transduction in alternate photic environments. Results are discussed in light of the available evidence on photopigment structure, morphological specialization and biogeographic distributions over geological time.