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Information on the reproduction in scleractinian solitary corals and in those living in temperate zones is notably scant. Leptopsammia pruvoti is a solitary coral living in the Mediterranean Sea and along Atlantic coasts from Portugal to southern England. This coral lives in shaded habitats, from the surface to 70 m in depth, reaching population densities of>17,000 individuals m−2. In this paper, we discuss the morphological aspects of sexual reproduction in this species. In a separate paper, we report the quantitative data on the annual reproductive cycle and make an interspecific comparison of reproductive traits among Dendrophylliidae aimed at defining different reproductive strategies. The present study on L. pruvoti is the first in-depth investigation of the reproductive biology of a species of this genus. As expected for a member of the family Dendrophylliidae, L. pruvoti is a gonochoric and brooding coral. The gastrodermal tissue of the gametogenetic mesenteries we examined was swollen and granular, which led us to hypothesize that interstitial cells could have a trophic function favoring gametogenesis. Undifferentiated germ cells arose in the gastrodermis and subsequently migrated to the mesoglea, where they completed gametogenesis. During spermary development, spermary diameter increased from a minimum of 14 μm during the immature stages to a maximum of 410 μm during the mature stages. As oogenesis progressed, we observed a gradual reduction in the nucleus to cytoplasm ratio due to the steady synthesis of yolk. During the final stages of oogenesis, after having migrated to the extreme periphery of the oocyte and having firmly adhered to the oolemma, the nucleus became indented, assuming a sickle or dome shape. We can hypothesize that the nucleus’ migration and change of shape may have to do with facilitating fertilization and determining the future embryonic axis. During oogenesis, oocyte diameter increased from a minimum of 20 μm during the immature stage to a maximum of 680 μm when mature. Embryogenesis took place in the coelenteron. We did not see any evidence that even hinted at the formation of a blastocoel; embryonic development proceeded via stereoblastulae with superficial cleavage. Gastrulation took place by delamination. Early and late embryos had diameters of 204–724 μm and 290–736 μm, respectively. When released, the larvae had completed ontogenesis and swam by a ciliary movement with the aboral pole at the anterior, their shape varied from spherical to cylindrical (in the latter the oral–aboral axis measured 695–1,595 μm and the transversal one measured 267–633 μm). [ABSTRACT FROM AUTHOR]