The development of the azooxanthellate octocoral Dendronephthya hemprichi from spawned gametes to planula larvae has been described, using scanning electron microscopy (SEM). Development of fertilized eggs is holoblastic, occurring until the 32-cell stage either by superficial divisions or by total cleavage. The pseudospiral development from the eight-cell stage leads to round stereoblastulae, followed by the appearance of embryos with bizarre forms. All developmental stages until the mature planulae are negatively buoyant. The planulae have a densely flagellated surface, and swim actively. The duration of development to mature planulae followed a seasonal pattern, ranging between 27-45 h from summer (at 26?C) to winter (at 20?-21?C), and probably reflected temperature effects. Similarly, in summer the first cleavage furrow was observed 2 h after mixing the gametes, whereas in winter this did not occur for at least 4 h. A significant variation was noted in egg diameter and planulae size from different colonies collected at the same time (December 1990). Longevity and maximal competency periods of 100 and 65 days, respectively, were found for the planulae during JulySeptember 1990, suggesting a potential for long distance dispersal in the reef environment. Additional key words: Cnidaria, Octocorallia, development, Red Sea Three modes of larval development have been reported for octocorals to date: a) externally in broadcast spawners, b) by retention of larvae in parent colonies among brooders, or c) in mucous material adhering to the surface of the mother colony (Coma et al. 1995; Benayahu 1997). More than a hundred years ago the mode of cleavage of octocoral eggs had already been illustrated for several species (Kowalevsky & Marion 1883). A century later, embryogenesis and subsequent development into planulae have been documented for a variety of other octocoral species: the gamete spawners Sarcophyton glaucum (Benayahu & Loya 1986), Lobophytum crassum (Uehara et al. 1987), and Plexaura kuna (Lasker & Kim 1996); the brooders Xenia umbellata (Benayahu et al. 1988) and Heteroxeniafuscescens (Benayahu et al. 1989); and the surface brooders Parerythropodium fulvum fulvum (Benayahu & Loya 1983) and Clavularia hamra (Benayahu 1989). Species that spawn gametes provide a ready source for studies on early ontogenetic stages, as opposed to internal brooders for which detection of the developing larvae is complicated by the retention of the embryo a Author for correspondence. E-mail: denlit@ccsg.tau.ac.il in the parent colony (e.g., Babcock & Heyward 1986; Benayahu et al. 1992). Octocorals generally have fairly yolky eggs that undergo holoblastic cleavage (e.g., Benayahu & Loya 1983; Benayahu 1989; Uehara et al. 1987; Lasker & Kim 1996). Their development includes a tendency to superficial cleavage, production of a solid embryo (stereoblastula), and a later transfer of nutritive substances into the archenteron concurrent with germ layer formation (see also Mergner 1971). There are still gaps in the descriptions of various embryonic stages in octocorals, and timing of the developmental events has not been completely mapped. If questions of larval structural or behavioral features, or their longevity and competence, are to be investigated quantitatively, planulae must be raised through to settlement (Babcock & Heyward 1986). In order to accomplish these goals such a study should be preceded by detailed examination of the embryonic cascade, including both structural and temporal aspects. The importance of Octocorallia on many Indo-Pacific reefs, and the lack of information on reproduction of species of the family Nephtheidae (order Alcyonacea), have led us in recent years to examine various aspects of their life history (Benayahu et al. 1992; Benayahu 1997). The azooxanthellate reef-inhabitants of This content downloaded from 157.55.39.180 on Mon, 25 Apr 2016 07:05:15 UTC All use subject to http://about.jstor.org/terms