A model of host–parasite relationships is proposed and its properties examined.

1. Serial sections were examined of thoraces of a selected strain of Aedes aegypti infected with either Brugia pahangi or subperiodic B. malayi and of wild-caught Mansonia uniformis infected with the latter parasite.

2. A few badly damaged flight muscle fibres are seen in the early stages of infection but many more fibres are destroyed at the time when the mature filarial larvae leave the muscle and enter the haemocoel. In the intervening period, when the larvae are growing within the muscle fibres, only minor damage develops, affecting nuclei and/or mitochondria. The nature of such minor damage and the mechanism of complete muscle breakdown differs in the two species of mosquitoes.

3. It was concluded that the muscle damage was sufficiently severe to explain the significant mortality often observed among experimentally infected mosquitoes at the time when the mature filarial larvae enter the haemocoel.

I am very grateful to Dr W. W. Macdonald, of the Liverpool School of Tropical Medicine, who supplied the Aedes aegypti mosquitoes and who has given invaluable help and advice throughout this study. Mr Cheong Weng Hooi and his colleagues in Kuala Lumpur kindly supplied, and partly processed, the Mansonia uniformis mosquitoes. Miss M. A. Johnson assisted with the care of the A. aegypti colony and Mrs J. Oliver helped with some of the histological work.

A population of three-spined sticklebacks, Gasterosteus aculealus, from a pond in Somerset was sampled about every three weeks for 19 months, a total of 1863 fish being collected. Three species of parasites were found in the fish: Schistocephalus solidus, Diplostomum gasterostei and Echinorhynchus clavula.

Seasonal changes in the incidence and intensity of the three parasitic infections are described. In general the infections increased in summer and autumn and decreased in winter and spring, although in Schistocephalus the differences in the level of infection between the two years were greater than between seasons.

The largest increases in the Schistocephalus and Echinorhynchus infections occurred in August and September and in the Diplostomum infection in May and June. These increases could be related to the feeding activity of the sticklebacks and to the abundance and level of infection of the Cyclops, Asellus and Limnaea pereger populations.

Reduction in the sizes of the infections was by predation and death of heavily infected fish in the case of Schistocephalus and Diplostomum and mainly by death of individual worms in Echinorhynchus.

These mechanisms are shown to be adapted to the life cycles of the parasites.

I am most grateful to Dr H. D. Crofton for his help and encouragement during this investigation and to Dr R. A. Avery for useful discussions and advice. This work was supported by a Science Research Council research studentship and a NATO studentship.

All three species of parasites found in sticklebacks from Priddy had overdispersed distributions, similar in shape to host–parasite distributions described by other authors.

The distributions of both Echinorhynchus clavula and Diplostomum gasterostei were fitted closely by the negative binomial. The values of k were similar for both species, being always less than unity; the Diplostomum distributions were more overdispersed and therefore had higher values of p.

The Schistocephalus distributions were mostly described by the log normal, but the high percentage infection and relatively low overdispersion meant that the fit was often not close. There was also some truncation at the upper end.

The relationship between the parameters of the negative binomial (p and k) and the shape and parameters of the original distribution have been investigated, both theoretically and with respect to the distributions of the stickleback parasites.In general p varied as the overdispersion and k as the percentage infection.

The advantages of an overdispersed distribution to the host and parasite populations are discussed and related to the life cycles of the parasites.

I am most grateful to Dr H. D. Crofton for his help and encouragement during this study, and to the staff of the Computer Unit, University of Bristol for their assistance with programming problems. This work was supported by a Science Research Council research studentship and a NATO studentship.

A population of Gasterosteus aculeatus from Priddy pool in Somerset was infected with three species of parasites: Schistocephalus solidus, Diplostomum gasterostei and Echinorhynchus clavula. The variations in the incidence and intensity of the infections with the sex, age and size of the sticklebacks are described.

The infections with the three parasites were very similar in male and female sticklebacks. The weights of Schistocephalus were greater in the females, however;the mean weight of the plerocercoids was larger suggesting that they grew more rapidly in female fish.

The Schistocephalus infection increased in small fish, under 1 year of age, but in older larger ones the infection decreased. These changes can be related both to the feeding habits of the fish and to the weight relationships of host and parasite.It was found that the weight of Schistocephalus did not greatly exceed that of the fish, and also that the combined weight of fish plus Schistocephalus was rarely greater than 3 g. Therefore the proportional weight of Schistocephalus, or parasite index, was lower in sticklebacks heavier than about 1·5 g.

The Diplostomum and Echinorhynchus infections both increased with age and size of fish, but the largest sticklebacks were not the most heavily infected. These increases can be related to the feeding habits of the fish in the case of Echinorhynchus and to accumulation with time in the case of Diplostomum.

In all three species the largest and oldest fish were not the most heavily infected.It is suggested that the old fish are becoming senile and are therefore less able to support large parasite burdens.

I am very grateful to Dr H. D. Crofton for his constant advice and encouragement during this study, and to Dr R. A. Avery for useful discussions. This work was supported by a Science Research Council research studentship and by a NATO studentship.

Clavella uncinata (Muller) (Crustacea: copepoda) was found infesting 24% of 1352 whiting Odontogadus merlangus (L.) examined from the North Irish sea.A study of the dimensions of the adult female and a comparison of the morphology of copepodid larvae from the Clavella of whiting and pollack Pollachius pollachius (L.) suggests that the Clavella from these gadoids are all one species. Observations on the process of feeding and histochemical analysis of the gut contents indicate that the parasites feed by browsing on the superficial tissues of the whiting and that the mouthparts are used more for the gathering of food towards the mouth than for cutting. Observations show that the hatching of eggs and the behaviour of the nauplii are remarkably similar to these functions in free-living copepods. Examination of Clavella from adult and young whiting, and from living specimens kept alive on the fish, suggests that there are definite cycles of development, that the eggs take about 21 days to mature and that adult Clavella has a life span of no more than 6 months.

I would like to thank the Masters and crews of the R.V. Cuma and R.V. Silver Spray and the staff of the Marine Biological Station, Port Erin for their help in the collection of material. I am especially grateful to Mr D. J. Slinn who guided me throughout this work and to Mr R. Moore for his technical assistance.

A piroplasm was isolated from a wild-caught Psammomys obesus from the lower Jordan Valley. In wild-caught Psammomys the infection is submicroscopic or of very low intensity, but rises sharply following splenectomy. The animal from which the piroplasm was isolated died with a 44 % parasitaemia and haemoglobinuria, following splenectomy.

The piroplasm was transmissible to clean, laboratory-bred Psammomys, to hamsters and Meriones. It was not transmissible to, or gave rise only to transient infections in, adult mice, rats, Mastomys, Acomys and Arvicanthis. Suckling mice and rats showed low parasitaemias for a few days, although division forms of the parasite were observed.

No protective cross-immunity with Nuttallia danii was observed.

On the basis of its measurements, spectrum of infectivity to experimental animals and absence of cross-immunity with N. danii, the piroplasm of Psammomys is considered to be a new species.

The name Nuttallia meri, sp.nov. in memory of the late Prof. Gr. G. Mer, is proposed for this piroplasm of Psammomys obesus.

I should like to express my appreciation of the excellent technical assistance provided by Mrs Miriam Sarfatti and Mr A. Bortinger, and to thank Dr Y. Schlein for his help with some of the drawings. I am particularly indebted to Dr A. Hadani of the Kimron Veterinary Institute for providing me with Meriones and testing N. meri in his laboratory.

This study was supported by the Reubin Kunin and Samuel Lunenfeld Medical Research Foundation - to which grateful acknowledgement is made.

The ultrastructure and development of Histomonas meleagridis in the reproductive tract of male Heterakis gallinarum has been described. In the testis the protozoon is a relatively large amoeboid organism which lies between the epithelial cells of the testis and the spermatogonia, spermatocytes and spermatids. It is similar in appearance to the invasive stage which is found in the final host and like the invasive stage, it also feeds upon the host cells by phagocytosis. In the vas deferens the protozoon lies between the host cells, where it is much smaller than the stages in the testis but still amoeboid, and inside the cells of the vas deferens.Intracellular stages are much smaller than the other stages, are rounded in appearance and cause little or no damage to the host cell. They are similar to the stages found in oocytes of the female nematode. The possible role of the male nematode in the life cycle of the protozoon is discussed.

I wish to thank Mrs B. Fisher for technical assistance and Mr B. Carter for assistance with the photography.

Seven daily injections of betamethasone given early in the infection adversely affect the immune response of rats and mice to Babesia microti and B. rodhaini. Betamethasone given late in the infection, when the parasitaemias are declining, causes recrudescences. The effects of betamethasone are reversible and those animals which survive the primary parasitaemia recover even if further courses of drug treatment are given. Betamethasone causes recrudescences of parasitaemia in some voles and field mice harbouring subpatent infections. Attention is drawn to the possibility that the therapeutic use of corticosteroids may enhance piroplasm infections and that elevated corticosteroid levels, resulting from stress situations, may affect latent piroplasmosis in wild caught rodents.

Descriptions are given of the first and second-stage larvae of Strongylus edentatus, S. vulgaris, S. equinus and Trichonema nassatum and newly hatched larvae of Trichonema catinatum and Triodontophorus serratus. Information has been obtained on the growth of pre-infective larvae and on the structural changes which occur during the first ecdysis. Most of the species of newly hatched larvae studied can be differentiated on the basis of differences in appearance, dimensions and other morphological features. The advantages of differential diagnosis of horse strongylid infection using first-stage larvae rather than infective larvae are discussed.

My thanks are due to Dr H. D. Crofton for his constructive criticism and advice and to Professor H. E. Hinton, F.R.S. for the provision of laboratory facilities.This work would not have been possible without the willing co-operation of Mr L. J. Potter from whose slaughterhouse the parasites were collected. I am also indebted to the Horse Race Betting Levy Board for their financial assistance.

This paper describes experiments to determine whether intestinal tissue mast cells and/or intestinal histamine are involved in the second, expulsive step of worm elimination. In neonatal rats, intestinal tissue contains only very little histamine and mature mast cells are encountered only sporadically. From birth to the adult age, there was a gradual rise in both intestinal mast cells and histamine.

During Nippostrongylus brasiliensis infection in the adult rat, the concentration of histamine in the small intestine was clearly lower than in uninfected controls.Especially low histamine values were found to occur on days 6–12 of a primary infection in the region where the main worm burden was located. Similarly, the number of tissue mast cells present in the epithelium of the jejunum was decreased in the same region and during the same period of time. From the observation that the bulk of the parasites are expelled at a time when histamme and mast cell levels are low, it was concluded that mast cells and their constituents were not an essential factor in the second step of worm elimination

This work was supported by the Schweizerische Nationalfonds zur Förderung der wissenschaftlichen Forschung (Grant 5200.3). The skilful technical assistance of Miss I. Beeger, Miss R. Keist and Miss M. Iseli is gratefully acknowledged. I thank Mr H. Berchtold, Biostatistisches Zentrum der Universität Zürich, for the statistical evaluation of the data.

The uninfected digestive gland of Bithynia tentaculata consists of three main cell types: ‘absorptive’ cells, ‘thin’ cells and ‘secretory’ cells. With infection by sporocysts, rediae, or metacercaria, pressure effects caused a reduction in the lumen of the digestive gland tubules and this probably resulted in a starvation autolysis. Some tubules recovered from infection and in such cases there was a reduction in the height of the epithelium. A migration of the digestive gland nuclei was only evident in redial infections and this may have been due to the toxic effects of rediae. In addition, rediae directly ingested host digestive gland tissue.The digestive gland was reduced to about two-thirds of its normal size in all heavily infected snails. Secretory cells of the gland were more resistant to infection than were the absorptive or thin cells.

I am indebted to Dr F. R. Stranack for her supervision and guidance throughout this investigation, and to Dr G. Charles and Dr T. Jenkins for their continued help and advice. This study was carried out during the tenure of a Research Assistantship awarded by the Governors of Portsmouth Polytechnic.

The penetration barrier presented to the miracidium by the snail epithelium can be divided into three layers. The chemical composition and physical configuration of the outermost of these plays an important part in the initial attachment response of the miracidium. Attachment can be stimulated in the absence of the snail by pure chemicals in solution. However, the surface to which the miracidium attaches must have the correct physical configuration otherwise the miracidium is unable to form a stable attachment.

In vivo, the miracidial body begins to contract and relax following attachment to the snail. This coincides with the start of secretion by the apical gland and accessory gland cells. The snail's columnar epithelium is rapidly cytolysed so that 10 min after attachment the anterior of the miracidium has reached the underlying connective tissues.

As the miracidium penetrates the snail, its ciliated epithelial cells are shed in sequence from anterior to posterior. This shedding removes a protective barrier against osmosis which is probably the acid mucopolysaccharide present in the epithelial cells. The mechanism of shedding is not understood but involves the reversal of binding by the desmosomal mucosubstance which attaches the epithelial cells to surrounding intercellular ridges.

The miracidium metamorphoses into the sporocyst as it penetrates the snail, by forming a new body surface. The material for this is extruded from the vesiculated cells which lie beneath the musculature of the body wall. The process of surface formation coincides with cell shedding and moves backwards as cells are shed. At not more than 2·5 h after attachment the extruded cytoplasm forms a thin continuous layer over the surface of the organism. Contacts with underlying cells appear to have been broken and the cytoplasm is underlain by a thin fibrous basal lamella. In the first 24 h after penetration the surface of this syncytium becomes thrown into folds and metamorphosis into the sporocyst can be considered complete.

An apparatus for the artificial feeding of tsetse has been described. Fresh defibrinated blood at 36 °C is circulated with a peristaltic pump through feeding capsules. The efficiency of the method has been compared with that of the Cockings' method and with the live host feeding. The flies exposed to feeding on this apparatus showed significantly higher feeding frequency than those allowed to feed on the Cockings' apparatus. Compared with the live host feeding, the feeding frequency for circulating blood method was slightly lower but the difference was not significant. Once the fly is induced to feed, it would in most cases complete engorgement unless disturbed. The rate of crop emptying in flies fed by the Cockings' method was abnormally slower as compared to those fed on the circulating blood. The present study indicates that for the successful artificial feeding of tsetse, it is essential to circulate the blood and regulate the temperature of the medium and the feeding surface to approximately 36 °C.

I wish to thank Mr S. B. Kutuza for technical help, and the Director of E.A.T.R.O. for permission to publish this work.

Adult specimens of Trochopus pini attach themselves by folding the disk-shaped haptor around the edge of the host's primary gill lamella. They are able to move from one place to another with the aid of disk-shaped pads on the head region.Ducts from the posterior median gland cells, which are extensive in the head region of the adult, open on the periphery of each disk and exude an adhesive secretion.

The oncomiracidium of T. pini is described and evidence is offered in support of direct invasion of the gills by these free-swimming larvae. Special attention is paid to the development of the head region of the parasite. Newly attached larvae lose their eye lenses and possibly their anterior median gland cells; their lateral head glands are well developed and most probably serve for attachment of the head region, since the posterior median gland cells are poorly developed and appear to have no ducts. Later the posterior median gland cells and their ducts increase in numbers and, in association with the pads on the head region, take over from the lateral glands the job of attaching the head region.

The paths of the tendons associated with the accessory sclerites on the haptor of T. pini indicate that this gill parasite has evolved relatively recently from the ancestors of benedeniid skin parasites.

I am most grateful to Commander J. Pareira, the Director of the Aquario Vasco da Gama in Lisbon where most of this work was done, and to the Staff of the Aquario and especially to Mr A. Ferreira. I am indebted to the Calouste Gulbenkian Foundation for a generous grant which made this visit possible. I am grateful also to the Directors and Staff of the Laboratoire Arago, Banyuls, France, the Station Biologique of the University of Bordeaux at Arcachon in France, and the Laboratory of the Marine Biological Association of the United Kingdom at Plymouth, England. I would like to thank the Royal Society for a grant from the Browne Fund which enabled me to work at Banyuls in 1962 and for a Pergamon Travel Award which made it possible to visit Arcachon in 1967.