Using a range of infection techniques, the ability of cercariae of the ectoparasitic digenean Transversotrema patialense to infect 24 species of tropical freshwater fish is examined. Of the 24 species (from 11 families) it is possible to infect 21 (from 8 families) under laboratory conditions. Reproductive success (R) for T. patialense from the cercarial infection process to the production of viable eggs by adult flukes is estimated for infections on two fish hosts, the cyprinid Brwhydanio rerio and the characinid Cheirodon sp. in controlled laboratory conditions. To calculate R, separate estimations of parasite infectivity, survival, fecundity and egg viability were made on populations of both host species. The enhanced reproductive success (R) of T. patialense on Cheirodon sp. is the composite resultant of higher infectivity, lower mean expected adult fluke life-span and higher mean fecundity/surviving worm when compared with infections on B. rerio under identical experimental conditions. Different patterns of egg viability of the two hosts do not materially influence differential reproductive success. A variety of formal techniques for handling the interacting components of reproductive success are described. The relationship between these techniques and the concept of basic reproductive rate, R0 (Macdonald, 1957; Anderson, 1982) is assessed.

Parasite burden (by volume) was measured in female mice of three strains given single or concurrent infections of Mesocestoides corti and Taenia crassiceps. Significant suppression of T. crassiceps volume was observed over a range of M. corti inocula and occurred irrespective of whether M. corti was introduced before or after infection with T. crassiceps. Suppression of T. crassiceps volume was greatest with larger inocula of M. corti and with increased duration of M. corti infection. No significant difference was found in the intraperitoneal volume of M. corti from mice given single or simultaneous concurrent infections of M. corti and T. crassiceps. When M. corti were inoculated into mice with an established infection of T. crassiceps a significantly smaller volume of M. corti was retrieved at post-mortem from the peritoneal cavities of these mice, than from mice given just M. corti.

Environmental sex determination in the mermithid nematode Romanomermis culicivorax is examined in the context of parasite reproductive success and population regulation. Experimental results show that the sex ratio of the nematode within its mosquito host (Culex quinquefasciatus) is dependent on parasite density. Sex ratios are biased to females at low parasite burdens and to males at high parasite burdens. Low temperature further enhances female-biased ratios. The net effect of density-dependent sex determination on parasite and host population growth is shown to be critically dependent on the frequency distribution of parasite numbers/host. Mermithid parasite distributions within natural host populations show low degrees of aggregation relative to other helminth species. The population regulation of the parasite is examined with respect to environmental sex determination and parasite-induced host mortalities by means of simple mathematical models of the dynamics of parasite transmission via its life-cycle. The significance of regulatory constraints on population growth are discussed in relation to the use of mermithids as biological control agents of insect pests or disease vectors.

Evidence for the presence of 11 intestinal parasites in pre-school children from 4 rural villages in Ghana was obtained from an examination of stool samples. Striking differences were detected between the prevalence of some of the 6 common infections in the 4 villages. The prevalance of Ascaris lumbricoides varied from about 76% in one village (Oshiyie, coastal savanna) to apparently 0% in another (Akuma, forest zone). No differences in prevalence for any infection were observed to be sex dependent. Investigation of the relationship between age of the children and prevalance showed that the degree of prevalence of both A. lumbricoides and Trichuris trichiura had essentially levelled off by the time the children were 4 years old. There was no evidence to suggest that the prevalence of either Entamoeba sp. or spp. or hookworm was approaching a maximum value, even in the oldest children. These trends applied across the villages regardless of the differences in prevalence values for the infections. On average, the children of Oshiyie were found to harbour twice as many infections as the children of the other villages. The investigation of the prevalence data revealed evidence of associations between pairs of infections, particularly those involving hookworm and T. trichiura.

An epidemiological survey of the distribution and abundance of Diplostomum spathaceum in farmed rainbow trout (Salmo gairdneri) from Mill of Cantray trout farm (Nairn, Morayshire) involved monthly sampling of fish over a 3-year period. Diplostomurn metacercariae were present in both the lens and aqueous humour of infected fish, and these have been treated separately throughout the study. The infection period was normally between May and September each year and transmission of the parasite from snail to fish did not occur at temperatures below 10°C. The prevalence and abundance of both lens and humour metacercariae reached a maximum in September. The cleansing and application of a molluscicide (copper sulphate) to the raceways in spring resulted in a 56% reduction in the numbers of metacercariae infecting trout during the following summer. However, no further improvement in parasite control was recorded when the treatment was repeated in the following year. Experiments using caged fish indicated that diplostomiasis was confined to certain areas of the farm only and that the infection rate of rainbow trout with D. Spathaceum cercariae was correlated (P < 0·01) with water temperature. The results of the study indicated that it is possible by regular cleaning and use of molluscicides to keep the intensity of diplostomiasis at such a level that rainbow trout do not become severely affected. However, as with other parasitic diseases, a combination of control methods will probably be required to eradicate the disease completely from trout farms.

The in vitro uptake of gamma-emitting radionuclides by microfilariae of Dirofilaria immitis was investigated. Radionuclides tested were 133Ba, 207Bi, 82Br, 109Cd, 51Cr, 60Co, 59Fe, 203Hg, 125I, 54Mn, 32P, 125Sb, 75Se, and 65Zn. Only 207Bi, 59Fe, 203Hg, 54Mn, and 46Sc showed more than 2% of the available radioactivity to bind to the microfilariae. When tested for retention in vitro only 203Hg showed retention levels approaching 90%. Moreover, when dimethyl suiphoxide was incorporated into the medium at levels of 1% (v/v) the uptake of 203Hg could be increased by 3–5 times; no other radio-isotope tested responded in this manner. The uptake of 203Hg was directly related to temperature and time of incubation. Mercury, as mercuric chloride, was toxic to the microfilariae and respresents an impediment to the incorporation of high levels of 203Hg in microfilariae.

Investigations were carried out into the properties and localization of chitin synthase (EC 2.4.1.16) in connection with the formation of Ascaris suum egg-shells. The chitin synthase of eggs exhibited properties very similar to those found in other chitin-synthesizing organisms. It was stimulated by the presence of ATP, GlcNAc and Mg2+ with maximal activity at pH 7·0. In the phase of active chitin synthesis, during formation of the primary shell layers, chitin synthase was bound to the structures of the eggs. On completion of chitin synthesis in the eggs, the amount of the enzyme increased in the soluble fraction. Two forms of chitin synthase have been found in the eggs, namely an inactive (zymogenic) and an active form. Transformation of these two enzyme forms represents a key mechanism in the regulation of chitin synthesis in A. suum eggs.

Infective 3rd-stage larvae of three species of marine ascaridoid nematodes, Pseudoterranova (= Phocanema = Porrocaecum = Terranova) decipiens, Anisakis simplex and Phocascaris/Contracaecum sp. were cultured in vitro in 0·9% saline or Medium 199 at 37°C beneath an atmosphere of either air or 95% air:5% CO2 All three species responded to culture at 37°C by producing a new cuticle. The majority of P. decipiens completed ecdysis under all the culture conditions employed. Ecdysis in A. simplex was stimulated by a high concentration of CO2; this effect was particularly noticeable in saline cultures. Both A. simplex and Phocascaris/Contracaecum sp. developed more effectively in a nutrient medium than in saline.

Microfilariae of Dirofliaria immitis were labelled with 203Hg 2+in vitro and injected into irradiated mice and Beagle dogs. With irradiated mice it was possible to demonstrate microfilariae present in the blood and to detect 203Hg by external counting as long as 28 days after dosing. The 203Hg 2+ label had a half-time of 4–5 days; the amount of stable mercury in the labelling medium strongly influenced the survival of microfilariae in vivo. In dogs, external counting showed the lungs to be a major location of the microfilariae soon after reinjection into the host. Evidence was obtained that labelled microfilariae can circulate; however, the detection of dispersed microfilariae is difficult because of the relative insensitivity of the detecting system. For radiomercury the accumulation of the inorganic form in the liver and kidneys limits the long-term usefulness of 203Hg 2+ as a label if the organism being studied also accumulates in these organs.

Evidence from many sources indicates that, in several parasite–vector systems, flight ability, fecundity or gonotrophic concordance of vectors, are affected by parasites (including bacteria, rickettsia and viruses) and in some cases parasites cause well-documented pathogenic effects (see reviews, for example, by Lavoipierre (1958a) and Hawking & Worms (1961) on filaria; Molyneux (1977, 1983) for trypanosomatids; Killick-Kendrick (1979) for Leishmania).

The frequency distribution of parasites in hosts commonly follows a negative binomial or similar distribution. Under certain conditions the magnitude of parasite-associated host mortality can be estimated by comparing the tail of the observed distribution to that of the distribution predicted from the first few points of the data. For the technique to work the following assumptions need to be met: mortality in lightly infected fish must be rare; infection and consequent mortality occur only in fish younger than those sampled; and the frequency distribution of the parasite at the time of infection should conform to a known probability distribution. The method was applied to frequency distributions of blastocysts of Callitetra rhynchus gracilis in 898 Saurida tumbil (Bloch) and 5013 S. undosquamis (Richardson). Parasite-associated mortality in S. tumbil was calculated to be at least 11 % in males and 2% in females. For S. undosquamis, estimated mortality was about 5% in males and 3% in females. The numbers of parasites estimated to produce a 0·5 probability of death, the parasitological equivalent of an LD50 were 3·4 and 5·7 for S. tumbil males and females, and 18 and 3 for S. undosquamis males and females respectively.

A deterministic model of the population biology of the non-infective free-living phase of Ostertagia ostertagi is described and tested. A comparison of field and laboratory studies indicates that the pre-infective larvae of O. ostertagi spend about twice as long in this phase in the field as in laboratory culture (13 days and 7 days respectively at 15 °C), and that the subsequent transition (i.e. second moult) to the infective phase also proceeds at a much slower rate (about 10 times less at 15 °C) in the field. Because of this discrepancy, estimates of model parameters are based entirely on measurements from field studies. A two-parameter model of pre-infective development in the field is derived. It describes egg and larval development as a direct non-linear function of air temperature. We also show that the mortality of the eggs and pre.infective larvae increases with temperature (although this relationship probably also subsumes a dependence on faecal moisture content). The model is shown to be a good mimic of the population dynamics of the non-infective free-living phase when tested against an independent data set, and is the basis of a larger model of the epidemiology of ostertagiasis.

The karyotype of Transversotrema patia1en consists of 10 pairs of chromosomes (2n = 20) of which 5 pairs are metacentrics and 5 pairs are submetacentrics. The chromosomes are large and range in size from 5 to 12 μm. The total chromosome length of the diploid complement is 16783 μm. Stages of spermatogenesis including the two gonial divisions and two reduction divisions leading to production of spermatozoa occur in cercarial embryos inside snail tissue, while the maturation divisions of the ovum occur in eggs freshly liberated by the fluke. The chiasma frequency is high, being 3888/cell and 388/bivalent. Cytological data indicate an independent phylogenetic status for the family Transversotrematidae.