JSTOR is a not-for-profit service that helps scholars, researchers, and students discover, use, and build upon a wide range of content in a trusted digital archive. We use information technology and tools to increase productivity and facilitate new forms of scholarship. For more information about JSTOR, please contact support@jstor.org.. British Ecological Society is collaborating with JSTOR to digitize, preserve and extend access to Journal of Animal Ecology. SUMMARY(1) We used an experimental protocol that allowed us to distinguish the relative influences of egg load and experience with host contact on foraging behaviour and clutch size decisions in the gregarious parasitoid Aphytis lingnanensis Compere. Egg load was manipulated without concurrent changes in experience by exploiting sizerelated variation in fecundity and by holding parasitoids at different temperatures to vary the rate of egg production.(2) Egg load influenced the intensity of searching behaviour. Parasitoids with smaller egg loads required more time within a foraging arena to discover hosts.(3) Parasitoids with smaller egg loads and parasitoids with a prior experience with host contact deposited smaller clutches.(4) Total host handling time was inversely related to parasitoid egg load. Increased egg load had a similar accelerating influence on each of the component activities that comprise host handling, including preparation for oviposition, oviposition, and postoviposition grooming and resting.(5) The probability of successful parasitoid egg to adult development was independent of clutch size. Progeny size, however, decreased with increasing number of competing sibs.(6) A. lingnanensis clutch size decisions do not conform to the static expectations of a forager maximizing the fitness gained per egg, per host, or per unit time. Rather, clutch size decisions appeared to be fundamentally dynamic, responding to changes in parasitoid physiology (egg load) and the parasitoid's perception of host availability (experience). Godfray & Ives 1988). Existing models therefore represent a hierarchical assemblage of techniques of increasing complexity, and models of different levels of complexity may be best suited for investigating theoretical issues or explaining the details of empirically observed patterns of oviposition.While the predictions of many models are in agreement, there are some noteworthy exceptions. Dynamic optimization models, which maximize lifetime reproductive success and employ dynamic state variables to describe the changing physiological condition of the foraging insect, predict that optimal decisions may vary over time in response to changing egg load, history of host encounters (henceforth 'experience'), and other variables (Iwasa, Suzuki & Matsuda 1984; Mangel 1987a, b, 1989a, b), whereas the remaining models generally predict fixed, optimal decisions for a host of given quality (e.g. Skinner 1985; Godfray & Ives 1988). Although modifications of models maximizing the rate of fitness gain to include constraints on egg production (...
Abstract. Direct behavioural assays were used to investigate the influences of host size and parasitoid egg load on the decision to host feed versus oviposit made by the parasitoid Aphytis lingnanensis Compere. Egg load was manipulated without concurrent influences on the history of host contact by exploiting size‐related variation in fecundity and by holding parasitoids at different temperatures to vary the rate of oocyte maturation. Host feeding comprised a series of feeding bouts, separated by renewed probing of the scale insect body. Successive feeding bouts were progressively shorter, suggesting that hosts represent ‘patches’ yielding resources at a decelerating rate. Parasitoids were significantly more likely to host feed on smaller hosts and oviposit on larger hosts. Neither egg load nor the treatment variables (parasitoid size and holding temperature) exerted significant influences on the decision to host feed versus oviposit on second instar (low quality) hosts. The failure to observe an effect of egg load on host‐feeding decisions was not simply a reflection of the parasitoids being entirely insensitive to egg load; significant effects of egg load on parasitoid search intensity and clutch size decisions were observed. Parasitoids developing on second instar (low quality) hosts experienced high levels of mortality late during development and yielded very small adults. The discord between these experimental results and predictions regarding the importance of egg load underscores the need for additional work on the proximate basis for host‐feeding decisions and the nutritional ecology of insect parasitoids.
Production of males in uniparental lines of two species in the parasitic wasp genus Aphytis was induced by rifampicin, and male sexual functioning was determined. Wolbachia-specific 16S rDNA primers were used in a PCR in order to: (1) assess correlation between thelytokous reproduction and the presence of Wolbachia; (2) detect the loss of Wolbachia DNA in uniparental A. lingnanensis following antibiotic treatments, with or without the presence of a host; and (3) clone and sequence part of the Wolbachia 16S rDNA from the uniparental Aphytis species for phylogenetic studies. Males produced viable sperm that was transferred to the female spermatheca following mating. However, sperm failure to effect egg fertilization resulted in all-male progeny. Wolbachia were found in the two uniparental (A. lingnanensis and A. diaspidis) but not in the two biparental (A. lingnanensis and A. melinus) Aphytis lines tested. They can be detected in wasps up to 7 days following antibiotic treatments, regardless of the presence of host. The 16S rDNA for the symbionts in the two Aphytis species is virtually identical, and is most closely related to the Wolbachia found in Muscidifurax uniraptor (Pteromalidae).
AdultMaladera matrida Argaman (Coleoptera: Scarabaeidae: Melolonthinae) males emerge from soil for an active period at dusk, a few minutes before the females. Adults are found during most of the active hours on the foliage in aggregations composed of an equal sex ratio. The mechanism of aggregation behavior ofM. matrida beetles was studied in a Y-shaped olfactometer. No evidence was found for the existence of an aggregation pheromone released either by males or by females, but behavior tests indicate that adultM. matrida beetles, males as well as females, are attracted to volatiles of an injured host plant. The following scenario is suggested: Males emerge daily from soil at dusk, a few minutes before the females, and immediately start feeding. Additional males are attracted to the injured host's volatiles and form aggregations. When females emerge from soil, the attractant volatiles are concentrated in spots, and the females join the aggregations, forming an equal sex ratio.
In parasitic Hymenoptera, severe sex ratio distortions are sometimes associated with the presence of symbiotic microorganisms. Symbiont-induced uniparental reproduction is found in several species of the genus Aphytis and is suspected in others. These intracellular bacteria (called Wolbachia) reside within the egg cytoplasm. In order to follow their vertical transmission, the distribution pattern of the symbionts in ovaries and eggs of two uniparental lines (A. lingnanensis and A. yanonensis) was studied by electron, confocal, and two-photon microscopy. The results obtained suggest that Wolbachia move from nurse cells to developing oocytes. In freshly laid eggs, the symbionts are concentrated in the posterior pole, away from the micropyle, and in later stages of embryogenesis they are found surrounding nuclei throughout the embryo.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
hi@scite.ai
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.