No abstract

gamma-Aminobutyric acid (a simple amino acid and potent neurotransmitter in human brain and other tissues of higher animals) and certain of its congeners rapidly and synchronously induce planktonic larvae of the red abalone, Haliotis rufescens, to settle and commence behavioral and developmental metamorphosis. These naturally occurring inducers of algal origin apparently are responsible, in part, for the substrate-specific recruitment, induction of settling, and the onset of metamorphosis of abalone and other planktonic larvae upon specific algae which provide naturally favorable habitats for the young of these species in coastal waters. These observations provide a convenient experimental model for further analysis of the basic molecular mechanisms by which environmental and endogenous factors control the recruitment and development of planktonic larvae. Halogenated organic pesticides significantly interfere with larval settling, as quantified in a new bioassay based upon these findings.

Addition of hydrogen peroxide to seawater causes synchronous spawning in gravid male and female abalones, and certain other mollusks as well. This effect is blocked by exposure of the animals to aspirin, an inhibitor of the enzyme catalyzing oxidative synthesis of prostaglandin endoperoxide. Hydrogen peroxide activates this enzymatic reaction in cell-free extracts prepared from abalone eggs (a very rich source of the prostaglandin endoperoxide synthetase); this effect appears to reveal a fundamental property of prostaglandin endoperoxide synthesis. Applicability of these findings to both mariculture and medical purposes is suggested.

Larvae of the scleractinian coral Agaricia humilis settle and metamorphose in response to chemosensory recognition of a morphogen on the surfaces of Hydrolithon boergesenii and certain other crustose coralline red algae. The requirement of the larva for this inducer apparently helps to determine the spatial pattern of recruitment in the natural environment. Previous research showed that the inducer is associated with the insoluble cell wall fraction of the recruiting algae or their microbial epibionts, and that a soluble but unstable fragment of the inducing molecule can be liberated by limited hydrolysis, either with alkali or with enzymes specific for cell wall polysaccharides. We now show that the parent morphogen can be solubilized by gentle decalcification of the algal cell walls with the chelators EGTA or EDTA, suggesting that the morphogen may be a component of the calcified recruiting alga itself, rather than a product of any noncalcified microbial epibionts. The solubilized inducer is subsequently purified by hydrophobic-interaction and DEAE chromatography. The purified, amphipathic morphogen retains activity when tightly bound to beads of a hydrophobic-interaction chromatography resin, and this activity (tested with laboratory-reared larvae) is identical in the ocean and the laboratory. We have attached the purified, resin-bound inducer to surfaces coated with a silicone adhesive and thus produced a potent artificial recruiting substratum--i.e., a morphogen-based chemical "flypaper" for A. humilis larvae. This material should prove useful in resolving the role of chemosensory recognition of morphogens in the control of substratum-specific settlement, metamorphosis, and recruitment and in the maintenance of species isolation mechanisms in the natural environment.

No abstract