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Spermatophore Deposition (spermatophore + deposition)
Selected AbstractsGamete production and sexual size dimorphism in an insect (Orchesella cincta) with indeterminate growthECOLOGICAL ENTOMOLOGY, Issue 2 2002G. Ernsting Abstract 1. The relationship of growth and body size with reproductive effort in animal species has been studied much less for males than for females. This imbalance applies to Orchesella cincta (L.) (Collembola), an insect with indeterminate growth, in which egg production is related positively to body size and negatively to growth. 2. To allow a comparison of the reproductive effort of male and female O. cincta, development and growth in immature stages of both sexes, and growth and spermatophore production for adult males were studied. 3. Embryonic development time and hatchling size did not differ between prospective males and females, but from hatching on the trajectories diverged, with males growing more slowly and maturing earlier and at a much smaller body size than females. 4. Neither the number of spermatophores deposited in the first adult instar (= inter-moult period) nor the total number of spermatophores deposited during seven instars was related to body size or growth. 5. Differences in growth rate between instars with and without spermatophore deposition indicated that the physiology of spermatophore production inhibits growth, which, however, was compensated for during the next instar. 6. The difference in the relationship of gamete production with body size and growth between males and females explains the divergence of their size at maturity. [source] When do the Costs of Spermatogenesis Constrain Sperm Expenditure?ETHOLOGY, Issue 1 2009Remarks on the Pattern of the Spermatogenic Cycle The costs of spermatogenesis constrain sperm expenditure when sperm production per day is limited. Thus, males are challenged to allocate available resources to sperm production and other life history functions. However, this prevailing assumption is not applicable to species in which spermatogenesis becomes quiescent during the breeding season. Males of these species prepare large quantities of sperm before the breeding season. Among these species, constraints on ejaculates have been intensively investigated in salamanders that deposit spermatophores. Although it is predicted that sperm expenditure should not be limited because of abundantly prepared sperm, spermatophore deposition is often limited during the breeding season when vas deferens are full of sperm. We tested a hypothesis regarding limited spermatophore deposition by measuring sperm quantity and volume of spermatophores sequentially deposited by male eastern newts Notophthalmus viridescens. A male newt rarely deposits more than three spermatophores per mating. If depletion of non-sperm components of spermatophores limits spermatophore deposition, we predicted that spermatophore volume decreases while sperm quantity remains constant as a male deposits more spermatophores. Alternatively, some regulative mechanisms allow a limited portion of available sperm to be expended per mating, in which sperm quantity is predicted to decrease while the spermatophore volume remains constant. Finally, depletion of non-sperm components may regulate sperm expenditure, which predicted that both spermatophore volume and sperm quantity decrease. We found that both sperm quantity and the spermatophore volume decreased as a male deposited more spermatophores during a single mating. Sperm expenditure was constrained without the costs involved in active spermatogenesis, and depletion of non-sperm components likely regulate sperm quantity loaded in spermatophores. In dissociated spermatogenesis, constrained sperm expenditure do not mean that costly spermatogenesis is directly limiting male mating capacity but rather suggest that the evolution of physiological mechanisms regulating sperm expenditure per mating maximizes male reproductive success. [source] Courtship in the Zig-Zag Salamander (Plethodon dorsalis): Insights into a Transition in Pheromone-Delivery BehaviorETHOLOGY, Issue 9 2005Amy L. Picard Courtship in plethodontid salamanders includes the delivery of male courtship pheromones by two distinct modes. Within the eastern Plethodon clade of the tribe Plethodontini, members of the Plethodon cinereus species group use an ancestral ,vaccination' mode of delivery, while members of the P. glutinosus group use an olfactory delivery mode. In order to shed light on this transition in delivery mode, I observed courtship behavior in P. dorsalis, a species that is phylogenetically intermediate to the P. cinereus and P. glutinosus groups. My observations indicate that P. dorsalis also is intermediate to the P. cinereus and P. glutinosus species groups in terms of courtship behavior. The context of delivery of male courtship pheromones in P. dorsalis is similar to that of the P. cinereus species group; however, the mode of pheromone delivery in P. dorsalis is olfactory. Thus, a transition in the context of pheromone delivery underlies the more obvious change in pheromone delivery mode. I discuss these findings in terms of the evolution of courtship pheromone delivery across the eastern Plethodon clade. I also report the first observations of ,premature' spermatophore deposition by male plethodontids. [source] | ||||||||||