Adaptive polyphenism produces alternative phenotypes depending on environmental stimuli. The water flea Daphnia pulex shows predator-induced polyphenism, facultatively forming neckteeth in response to kairomones released by Chaoborus larvae. This study was designed to reveal the regulatory systems producing the defensive morph during embryonic and postembryonic development. As noted previously, the crest epithelium at the site of neckteeth is shown to thicken earlier the neckteeth formation, and the neckteeth number increased until the third instar, and later disappeared. Exposure to kairomone at various time points and intervals during development showed that the signal was required even at early postembryonic stages to maintain neckteeth. Moreover, two different induction methods, i.e. embryonic and maternal exposures, enabled us to discriminate maternal and zygotic effects in response to kairomone. Direct embryonic exposure is shown to be sufficient to form neckteeth without maternal effect although their growth was diminished; namely, there is a trade-off for neckteeth production. However, maternal exposures resulted in larger progenies in smaller numbers, suggesting that the mother daphnids change their reproductive strategy depending on kairomone signals. Taken together, the developmental responses to the presence of predators are regulated elaborately at various levels.
Many organisms have the ability to alter their development in the presence of predators, leading to predator-induced defenses that reduce vulnerability to predation. In the water flea Daphnia pulex, small protuberances called 'neckteeth' form in the dorsal neck region in response to kairomone(s) released by predatory phantom midges (Chaoborus larvae). Although previous studies suggested that kairomone sensitivity begins when chemoreceptors begin to function during embryogenesis, the exact critical period was unknown to date. In this study, we investigated the period of kairomone sensitivity and the process of necktooth formation in D. pulex through extensive treatments with pulses of kairomone(s). First, we described the time course of embryogenesis, which we suggest should be used as the standard in future studies. We found the kairomone-sensitive period to be relatively short, extending from embryonic stage 4 to postembryonic first instar. We observed cell proliferation and changes in cell structure in response to the kairomone treatment, and propose a model for necktooth formation. Preliminary LiCl treatment suggests the Wnt signaling pathway involved in crest formation as a candidate for the molecular mechanism underlying this process. Our study provides basic insight toward understanding the mechanisms underlying adaptive polyphenism in D. pulex.
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