No description available.

An experimental study of laboratory populations of the stored-products moth, Cadra cautella (Lepidoptera: Phycitidae) and its larval parasitoid, Venturia canescens (Hymenoptera: Ichneumonidae) identified and quantified density- and age-dependent demographic characteristics of the host-parasitoid system. Host imago longevity and fecundity depended on larval weight at pupation. Observed effects of C. cautella larval competition for food on larval mortality, stage duration, and weight at pupation were successfully captured in a mathematical model. Host larval age significantly influenced inter-stage cannibalism and susceptibility to mortality resulting from parasitoid oviposition wounds. Both larval parasitoid developmental rates and adult parasitoid attack rates depended on host larval age. Long-term population experiments of host and host-parasitoid populations revealed that host populations fluctuated with a period slightly in excess of host generation time and that parasitoid populations were in synchrony with host populations.

This study is concerned with two strigeid genera which utilise fish as their second intermediate host and piscivorous birds as a definitive host, i.e. Apatemon (Apatemon) Sudarikov, 1959 and Ichthyocotylurus Odening, 1969. Although the lifecycle has been ascertained for most Ichthyocotylurus spp., confusion and disagreement still exist as to the constituent species, while all of the life-stages have been described for only a single member of the subgenus Apatemon (Apatemon). In order to clarify species membership to these taxa and indeed the taxonomic position of the subgenus Apatemon (Apatemon) further information was required on the life-cycles and life-stages of these strigeids. Although, metacercariae from this family have been recorded from a variety of British fishes, confirmed records, i.e. those supported with life-cycle data, are limited to a single species. It was this lack of confidence in identifying metacercariae recovered from fishes and the lack of known good criteria for distinguishing the adults that prompted the present study. Collections of metacercariae from a variety of hosts and locations were made, from which all subsequent life-cycle stages were obtained. The project aims were to establish the identity of the forms occurring in British fishes, by applying discriminatory techniques to the experimentally reared life-stages. In addition to traditional methods, techniques with little previous application to these genera were used and included, scanning electron microscopy (SEM), chaetotaxy, principal components analysis (PCA), and karyology. Furthermore, behavioural aspects such as the release patterns of cercariae from their molluscan hosts were studied to investigate whether they would prove to be of diagnostic value. Metacercariae obtained from the sampling survey were tentatively identified, using all currently employed methods for their determination, i.e. morphology, nature of cyst, host and site specificities, as Ichthyocotylurus erraticus (Rudolphi, 1809), I. variegatus (Creplin, 1825), Apatemon gracilis (Rudolphi, 1819) and A. annuligerum (Nordmann, 1832). Material collected from Finland was considered to contain both Ichthyocotylurus spp. recovered in the U.K., as well as I. platycephalus (Creplin, 1825) and I. pileatus (Rudolphi, 1802). The Ichthyocotylurus spp. were found to be more host specific than A. gracilis, although A. annuligerum was considered oioxenic to perch Perea fluiatilis L. Records of I. erraticus from gwyniad Coregonus lavaretus (L.) and grayling Thymallus thymallus (L.), and A. gracilis from arctic charr Salvelinus alpinus (L.) constitute first listings from Britain. The large number of sensilla present on the body surface of these metacercariae, observed by SEM and chaetotaxy, precluded their diagnostic use. PCA was, however, found to be of value for distinguishing between species and determining morphological variation within a species. I. erraticus, I. variegatus and A. gracilis adults were successfully reared in experimental hosts using metacercariae from a variety of fish hosts, sites within a single fish host and geographical sites. The adults obtained enabled clarification of the identities assigned to the metacercariae. Those metacercariae believed to represent I. pileatus and A. annuligerum failed to establish in experimental hosts. Herring gulls and lesser black-backed gulls proved to be extremely good experimental hosts for both Ichthyocotylurus spp., with the vast majority of infections establishing and providing high yields of eggs and adults. These infections yielded information on the establishment, development, fecundity, site specificity, longevity and morphological variability of the adults. Aspects of the morphology and biology of I. variegatus adults recorded were found to support its validity as a species discrete from I. platycephalus which was in some doubt. The experimental hosts used for A. gracilis infections, domestic and mallard ducklings, were found to be less satisfactory. Challenges were performed with A. gracilis metacercariae from three sources, rainbow trout, salmon parr and stone loach. The latter source was the only one to result in egg producing adults, with specimens exhibiting normal morphology and demonstrating an increased longevity over adults raised from salmonid metacercariae. These findings suggest that the metacercarial host may affect the successful completion of the life-cycle. Eggs of known origin were collected for all three cultured strigeid species, enabling further life-cycle studies, these were incubated and miracidia successfully raised. Developmental periods were found to be temperature dependent and differed for the three species at 20°C: A. gracilis < I. erraticus < I. variegatus. Light microscopy revealed the morphology of all three species to be identical, as were the epidermal plate formulae and chaetotaxy, indicated by silver-staining. The nomenclature for the distribution of miracidial sensilla derived by Dimitrov et al. (1989) was amended to enable a full description of these species. Osmotic shock resulted in an improved deciliation of the miracidia compared to sonication and subsequent SEM observation confirmed the arrangement of body surface structures, while revealing sensilla forms. Behavioural aspects of I. variegatus miracidia were examined, with a maximum longevity (< 11 hours) recorded at the lowest temperature studied (l0 degrees C), and host finding demonstrated to occur by an increased turning response in the presence of substances emitted from the susceptible snail host, following an initial unresponsive dispersal phase. Ichthyocotylurus cercariae were found in naturally infected Valvata piscinalis which constitutes the first record in Britain of cercariae of this genus. Cercariae of I. erraticus and I. variegatus were successfully raised experimentally from miracidia of known identity and origin within naive, experimentally raised V. piscinalis hosts, while A. gracilis cercariae were obtained from laboratory reared Lymnaea peregra. Cercarial developmental periods within the molluscan host were found to be temperature dependent and markedly different for the strigeid genera investigated, as were their behaviour and morphology. The Ichthyocotylurus spp. exhibit a distinct diurnal emergence rhythm from their molluscan host, being shed during the hours of daylight, while A. gracilis cercariae demonstrate a reciprocal pattern, emerging during the hours of darkness. Behavioural contrasts were also observed in longevities, emergence strategies (route of exit) and swimming behaviour. The two Ichthyocotylurus spp. were extremely similar, the only cercarial features found to be of diagnostic use were: the presence or absence of eye-spots; their differing developmental periods from miracidium to cercaria; the number and distribution of sensilla when compared by PCA; and their differing longevities at 20 degrees C. Characters considered to be of value in differentiating between strigeid cercariae at the species level, including the armature, chaetotaxy pattern and resting posture, did not differ between these two species. SEM observations enabled descriptions of the variety and structure of sensilla present on different life-stages, while transmission electron microscopy revealed the internal structure of cercarial sensory structures. Experimentally raised cercariae were found to be infective and the life-cycle was completed for the three strigeid species. Host specificities were observed for I. erraticus and A. gracilis, being particularly stringent for the latter species, while site specificities recorded were as observed in natural infections. Metacercarial maturation periods (for encystment) were highly temperature dependent, being comparable for the two Ichthyocotylurus spp. and more rapid than for A. gracilis specimens.

No description available.

Some parasites may modify the behavior of their hosts. Altered behaviors may: 1) benefit the host in that they defend against the pathogen, 2) benefit the pathogen and represent manipulations of the host response, and 3) benefit neither the host or the pathogen and simply be a product of the host response to infection. In this thesis I examine four host/parasite systems. For each system, I explore host/parasite behavioral interactions, and examine them with regard to selective pressures that may be acting on both the host and the parasite. I test the Hamilton and Zuk hypothese in 26 species of lizards. I find an inverse relationship between a lizard species' brightness and parasite prevalence. My result lend credence to criticisms of the Hamilton and Zuk Hypothesis. If infection does occur, animals may alter their behavior to impair the growth and reproduction of the parasite. To test this prediction, I examine behavioral thermoregulation in two strains of the snail Biomphalaria glabrata, one resistant to, and one susceptible to, the parasite Schistosoma mansoni. The preferred temperature of infected snails drops five weeks after exposure to the parasite. I propose the hypothesis that pathogen-induced host defense responses result in altered host behaviors and enhanced predation. In particular, I examine the effects of the acute phase response (a physiological response whose symptoms include fever, reduced activity and malaise) on antipredatory behavior in bullfrog (Rana catesbeiana) tadpoles. This host response is associated with the preliminary stages of infection with many pathogens yet its behavioral effects have received little attention. I find that the stereotypical effects of the acute phase response can lead to increased predation. I suggest that altered behaviors may afford some parasites a potential pathway to their next host. I examine the behavioral effects of a yeast, Candida spp., a single-host parasite species in its natural host, the red-legged frog (Rana aurora). Infected tadpoles exhibit the same behavioral modifications that are noted in bacteria injected bullfrog tadpoles. These results suggest that some altered behaviors may occur due to a host response to infection and not due to parasitic manipulation. / Graduation date: 1993

From simple beginnings, when only one host was required, numerous parasitic organisms have evolved complex life-cycles involving two or more host species. For example, trematode parasites reproduce in vertebrates, their definitive host, but their current life cycle also typically involves two intermediate hosts that were added during the course of evolution. Vertebrates are often considered to be the ancestral hosts of trematodes although other scenarios exist. While multi-host life cycles are observed in distantly related groups of parasites, their evolution remains largely unexplored. In trematodes, while recent phylogenetic studies have shed light on the sequence along which the different hosts were incorporated in the cycle, conditions that favoured the evolution of such complex life cycles can only be hypothesized. However, one opportunity to understand the force shaping the evolution of complex life cycles is provided by the few trematode species in which the classical three-host cycle facultatively reverts to a shorter cycle (i.e. life cycle abbreviation). In this study, the effects of different environmental factors on the life history strategy of the trematode Coitocaecum parvum were investigated using laboratory and field studies. C. parvum is able to abbreviate its life cycle from three to two hosts by maturing early (i.e. progenesis) and producing eggs inside the second intermediate host; both life history strategies occur simultaneously in C. parvum populations. Environmental factors such as predator densities should strongly influence parasite life history strategies. In fact, this study shows that laboratory reared Coitocaecum parvum adopt preferentially the normal three-host cycle when chemical cues from the definitive host are added to their environment, while the shorter cycle is favoured when these cues are absent. However, in nature, multiple environmental factors are likely to be perceived by parasites. Consequently, C. parvum�s ability to adapt its developmental strategy to definitive host densities may be confounded by the complex combination of various environmental parameters. Within-host competition between parasites sharing a common host is also likely to influence individual life history strategies. Parasites could then use alternative life strategies to adaptively respond to intraspecific and interspecific competition. Indeed, this study found that C. parvum preferentially adopts the abbreviated cycle in the presence of competitors. However, in interspecific competition, C. parvum�s strategy also depends upon the competitor species, possibly influenced by the other species� transmission route. Furthermore, intensity of intraspecific competition proved to constrain C. parvum�s ability to use the abbreviated life cycle. Finally, genetic relatedness between co-infecting C. parvum individuals seems to affect parasite life strategy through kin selection: closely related individuals are more likely to adopt the same developmental strategy, when they share a host, than unrelated ones. C. parvum individuals adopting the abbreviated cycle are enclosed within a cyst in their intermediate host and must produce eggs by self-fertilization, the most severe case of inbreeding. It was hypothesized that their offspring would have reduced fitness due to inbreeding depression, therefore selecting against the shorter cycle. However, this study found no difference in the survival and infection success of offspring produced through the abbreviated and normal cycles. Furthermore, no evidence for a genetic basis of life cycle abbreviation was detected: the same proportion of offspring from both reproductive strategies adopted the shorter life cycle. The work in this thesis provides evidence that although life cycle abbreviation provides Coitocaecum parvum with a viable alternative life strategy, numerous factors promote or restrict the adoption of this strategy. While this life history strategy has no detectable effect on parasite fitness, both environmental parameters and within-host competition affect C. parvum life-history strategies, alternatively selecting for either the shorter or normal life cycle. Overall, the complexity of the parasite environment could maintain both developmental strategies in C. parvum populations and, on a broader scale, could have influenced the evolution of complex life cycles in parasites.

Thesis (Ph. D.)--University of Adelaide, 1985. / Includes bibliographical references.

Thesis (M. Sc.)--University of Adelaide, 1984. / Includes bibliographical references (leaves 111-137).

Thesis (Ph. D.)--University of Adelaide, 1983. / Includes bibliographical references (leaves 218-251).

Thesis (Ph. D.)--University of Adelaide, Dept. of Plant Pathology, 1987. / Includes bibliographical references.