A new coccidian parasite, Caryospora dendrelaphis sp.nov., with endogenous stages in the duodenal epithelium is described from the Australian colubrid snake Dendrelaphis punctulatus (Gray).

Diclidophora merlangi was found to consume oxygen under a variety of experimental conditions. The Qo2 of homogenates was 0.415 μl oxygen consumed/mg wet wt/h. Oxygen uptake was reduced in the presence of inhibitors: cyanide 0.1 mM and 5.0 mM, 100%; rotenone 10−6 M, 56%; antimycin A10−6 M, 63 %; malonate 10 mM, 36 %; arsenite 5 mM, 46 %; fluoroacetate 5 mM, 47 %. Worms died after 1 h incubation in 1 mM cyanide. It is suggested that these data provide evidence for the existence of a functional TCA cycle and respiratory chain of the classical pattern in this fluke.

Eimeria weybridgensis sp.nov. is described from pure infections in experimental lambs. The characters by which it can be distinguished from E. ovina and E. crandallis, which it resembles, are described. Cross-infection experiments confirmed its distinction from E. ovina. Oocysts of E. weybridgensis are the same size as those of E. crandallis, measuring 24 × 17 μm. The prepatent period of E. weybridgensis, however, is much longer and the morphology of the sporocysts of the two species is different.

Acquired immunity to Schistosoma mansoni in the rat can be assayed by the recovery of a proportion of the schistosomula of a challenge infection from the lungs 5 days after the challenge has been given. The recoveries from immune rats, which are significantly less than those from control animals, demonstrate that a proportion of a challenge infection is killed in the lungs or at an earlier point in the pathway of migration.

Immunity in the Sprague–Dawley rat can first be shown by the lung recovery technique 3 weeks after an immunizing exposure of 500 cercariae. Immunity reaches a peak between weeks 6 and 7 but then declines to zero by week 12. The PVG inbred Hooded rat shows a similar but delayed development and decline of immunity. When the lung recovery technique shows immunity to be declining, hepatic perfusion demonstrates that immunity to reinfection is partially retained, indicating that at this stage the challenge is killed after the first 5 days.

Re-exposure of rats in which immunity has declined induces an anamnestic lung recovery response. There appears to be a relationship between spontaneous cure and the decline of immunity. A factor in the serum of infected rats which kills young schistosomula in culture develops in parallel with immunity, but high titres of this factor are maintained during the decline of immunity.

In order to study egg release by Aspiculuris tetraptera total faecal collections from infected mice were made every 1½ h throughout successive 24 h periods. This was done with the aid of a histokinette machine. The cage containing the mice was suspended from one of the arms of the machine and every 1½ h the cage was moved on by the machine to the next adjacent collecting dish. The faecal pellets passed were counted and then used for flotation egg counts.

It was found that eggs were not released steadily and continuously and, in the case of the worms in an isolated mouse, egg output was clearly intermittent. Egg production did not appear to vary with the faecal production of the host in a consistent way but with two groups of 8 mice it was highest when faecal production was at its peak shortly before dawn. For the groups of 8 mice the concentration of eggs per faecal pellet was also highest at this time. In two experiments with an individual mouse, however, the egg counts fell to zero at dawn before the level of faecal production became reduced.

It is suggested therefore that egg output by female A. tetraptera may be stimulated by the altered physiological state of the host associated with feeding or general activity.

The growth of male and female parasitic stages of Nematospiroides dubius from male and female ASH/CS1 mice was measured in terms of dry weight. No sex-linked resistance of mice to infection with N. dubius was apparent, as growth was the same in both sexes of host. The growth rate did not alter when moulting occurred.

All parasitic stages of N. dubius consumed oxygen in vitro and oxygen was also shown to be necessary for motility and survival.

The relationship between body size and metabolic rate was established for male and female parasitic N. dubius and the b values indicated that aerobic metabolism is of functional importance to this species.

The size/metabolism relationship for the whole life-cycle was established.

The ectoparasitic copepod Lepeophtheirus pectoralis exhibited a regular annual cycle of abundance on its hosts. Both the incidence and intensity of infection were greatest in August or September and both declined over winter to their minimum values in April. Very similar cycles were observed in both 1972 and 1973. Analysis of the age structure of the parasite population showed that the increase in abundance coincided with the onset of the breeding season. Although females always outnumbered males the sex ratio approached unity during the breeding season, which extended from May to October. Copulating pairs were most commonly observed during this period.

There was a marked bimodal peak of egg production each year, with the first mode occurring around May and the second mode around August or September. This pattern was produced by a system of alternation of generations operating within the parasite population, with a summer type generation (distinguishable by its rapid maturation rate and reduced longevity) alternating with an overwintering type of generation.

The numerical relationships between a population of Lepeophtheirus pectoralis and its host population (plaice) have been described. There was no significant difference between infection levels in male and female plaice. In most of the monthly samples (75%) there was no significant relationship between host length and either the incidence or intensity of infection. The samples in which significant positive correlations occurred were usually taken within the period November to April. It is probable that the immigration of smaller fish, with lower levels of infection, from shallower water produces this effect.

The parasite population was found to have an overdispersed distribution (variance > mean) within its habitat, the host population. The frequency distributions of numbers of parasites per fish were calculated and the negative binomial distribution was fitted to these. The fit was good in 22 of the 24 samples and the value of k, the exponent, was found to be directly related to the mean density of the parasite population. Iwao's (1970) method of dispersion analysis indicated that the observed negative binomial was generated by a model of randomly distributed clumps or colonies of individuals. A possible mechanism of producing this pattern was proposed based on evidence from studies of mortality in the parasite population (which indicated that all-or-none type mortality operates on the clumps at certain periods during the year), the infection process (which demonstrated that a single wave of infection produces an overdispersed spatial distribution) and the examination of parasites from individual fish (which displayed a clumping of parasites at certain stages rather than an even spread over the range of possible stages). The mechanism proposed is that the adaptations for host location of the infective copepodid stage tend to produce aggregations of these larvae in favourable areas of a heterogeneous habitat. Fish moving randomly into these areas will tend to be infected by more than one larva (a clump of larvae) at any one time when available for infection. The fish can be regarded as equivalent to random samples of the free larval population and the aggregated distribution of the parasite population on its hosts is therefore directly related to the aggregated distribution of the free-swimming infective larvae.

Of 63 specimens of the lizard Mabuya mabouya (Scincidae) examined in Pará State, Brazil, 31 showed one or more haemosporidians in the peripheral blood. These included Garnia (Plasmodium) morula (Telford, 1970), Lainson, Landau & Shaw, 1971; Plasmodium tropiduri and P. diploglossi Aragão & Neiva, 1909; a Plasmodium species close to P. diminutivum Telford, 1973a; and a new species of Saurocytozoon Lainson & Shaw, 1969a. Eleven different combinations of these parasites were noted, emphasizing the care needed in avoiding erroneous descriptions based on mixed infections. This is especially so when G. morula is mixed with P. tropiduri or other species with small, rounded gametocytes occupying a polar position in the red blood cells. Of 18 skinks infected with G. morula, 10 had pure infections, as judged by repeated examinations over long periods. The morphology of the Brazilian parasite is very similar to that described for G. morula from Panama (Telford, 1970): no malarial pigment could be demonstrated in any stage of the infection, including ookinetes and possible early oocysts which were studied in experimentally infected Culex pipiens fatigans. Ookinetes and rounded forms, possibly representing uninucleate oocysts, persisted in these insects up to 24 h after the blood-meal, but developed no further. C. p. fatigans is thus unlikely to be a natural vector of G. morula. Saurocytozoon mabuyi sp.nov. is described in M. mabouya: the gametocytes develop in the lymphocytes and monocytes of the circulating blood and reach maximum size in 19–28 days. The parasite can be distinguished from the other known species, S. tupinambi of the teiid lizard Tupinambus nigropunctatus, by its smaller gametocytes. Nothing is known of the sporogonic cycle. Differences between the sporogonic stages of S. tupinambi and Leucocytozoon are listed.

The larvae of Aspiculuris tetraptera were found in the mid-colon of mice within hours of infection. When the colon was divided into 10 equal sections the larvae were mainly found in sections 5, 6 and 7 during the first 6 days of the infection. The worms entered the crypts of Lieberkühn in this region on day 1 and remained there until day 4 or 5. After this time they left the crypts and returned to the lumen of the colon. On day 7 the worms emigrated anteriorly and thereafter were recovered only from the proximal region of the colon (sections 1–4), although in heavier infections a few larvae remained in the mid-colon.

The initial establishment site was the same in both Rattus norvegicus and in Apodemus sylvaticus, but an infection with A. tetraptera in the abnormal hosts, R. norvegicus and A. sylvaticus, was characterized by less than 7% of the inoculum becoming established, a slower rate of growth and a wider distribution centering around the preferred site. The small number of established larvae was lost from the rat before day 12 and from A. sylvaticus before day 8, whereas larvae persisted in laboratory mice for a longer period.

Lowland populations of the Plasmodium berghei group are compared with strains from the highlands of Katanga, Republic of Zaire, and it is concluded that the former warrant separate specific status. It is proposed that Plasmodium berghei yoelii of the Central African Republic be raised to a species, P. yoelii, and the lowland subspecies from the CAR, Brazzaville and Nigeria be moved to this species as P. y. yoelii, P. y. killicki and P. y. nigeriensis. P. berghei from Katanga would then revert to a monotypic species.

Differences between P. berghei and P. yoelii are in distribution, hosts, optimum temperatures of sporogony, sizes of mature oocysts and of sporozoites, rates of growth and minimum maturation times of tissue schizonts in the liver of the white rat, the forms of six enzymes and the DNA.

Differences between three subspecies of P. yoelii are in distribution, the sizes of mature oocysts and of sporozoites, sizes of tissue schizonts in the liver of the white rat, the effect of tissue forms on the nuclei of infected parenchymal cells and the electrophoretic forms of the enzyme GDH.

Young white mice were infected with different doses of eggs or cysticercoids of Hymenolepis nana and the subsequent faecal egg output was measured over a 3-day period. This was then correlated with worm numbers, determined after killing the hosts. The longest worm in each infection was measured and it was shown that crowding decreased the linear dimensions, number of eggs per proglottis and rate of proglottis production of these worms, but that their shape was not affected.

The relation between total egg output and worm numbers was complex. In both egg-derived and cysticercoid-derived infections the egg production rose to a peak, fell and then levelled off to a constant rate with increasing worm numbers. Cysticercoid-derived worms were larger than egg-derived worms, but produced approximately the same number of eggs per unit of biomass. The differences in the egg output curves for the two types of infection were interpreted as being due to their size difference; this in turn may be a consequence of the host immunological response.

Adult Oesophagostomum columbianum populations were larger in sheep fed low-protein diets than in adequately fed animals. Diet did not influence the numbers of larva which became established in sheep. Sheep fed high-protein diets eliminated more worms and were more immunologically competent than poorly fed animals. More encapsulated larvae, showing arrested development, were found in adequately fed sheep than in those fed low-protein diets. Adult O. columbianum produced eggs at an earlier time after infection in poorly fed sheep than worms in well fed sheep. More eggs/female worm were produced in sheep on a low-protein diet compared with the number of eggs produced in well fed hosts over the last week of the infection. The effects of immunity on the behaviour of the worm in both host diet groups is discussed.

There was a greater cellular proliferation in the intestines of infected adequately fed sheep than in infected animals on low-protein diets. These changes were most pronounced in the large intestine where the adult parasites were found. The macrophage-lymphocyte series of cells underwent hyperplasia in well fed animals but these changes were reduced, particularly among the plasma cells, in sheep fed low-protein diets. Increased mucin and mast cell counts were observed in sheep on high-protein, but not in hosts on low-protein diets: the intestinal populations of eosinophil and globule leucocytes were also reduced in poorly fed sheep.

The relationship of these various cellular reactions and their effect on the protective immunity of sheep to O. columbianum is discussed. It was concluded that the increased susceptibility of protein deprived sheep to O. columbianum infections was associated with malfunctions of the innate immunity of the gut, involving decreased peristalsis and failure of the mucin cell response, and with reduction of the adaptive immune response which was reflected by impoverished lymphocyte and plasma cell reactions, and possibly with poor cooperation between sensitized lymphocytes, antibodies and the mast cell-granulocyte effector mechanisms in protective immunity.

Using biomedical techniques experimental determinations of the hydrostatic pressure in the pseudocoel of adult female Philonema oncorhynchi indicated that the rate of increase in pressure (dP/dT) and absolute pressure values (cm/H2O) shown by bursting worms in distilled water are correlated with the diameter of the nematode. At bursting pressures, wall tension in a wide size range of worms was virtually identical, indicating that the bursting process is independent of muscular contraction. That the generation of the hydrostatic pressure was an osmotic phenomenon was confirmed by measuring dP/dT in prelarvigerous and larvigerous female worms subjected to different concentrations of sodium chloride, ranging from 89 to 800 m-osmol/kg, and also to a variety of solutions of similar osmolarity (155–175 m-osmol/kg), e.g. magnesium sulphate, urea, potassium chloride, sodium chloride and sucrose. The overall rate of uptake was faster in the larger worms but, per unit surface area, small worms had an uptake rate three times that of the large individuals.

The prediction that the body wall of female P. oncorhynchi is permeable to ions such as Na+ was confirmed using radiolabelled 22Na and by bringing about changes in the osmolarity of worms subjected, for 5 min periods, to hyperosmotic solutions of sodium chloride and sucrose. The survival of P. oncorhynchi in the body cavity of sockeye salmon, Oncorhynchus nerka, is dependent upon the permeable nature of the body wall of P. oncorhynchi allowing the worm to function as an ‘osmometer', because as the anadromous O. nerka enters fresh water, the osmolarity of its blood plasma is known to decrease by about 15%. At the time of spawning in Cultus Lake, British Columbia, the body fluids of both female P. oncorhynchi and O. nerka are isosmotic, indicating that the worms are able to equilibrate to the above changes and at the same time preventing premature bursting in the body cavity of its host. However, osmotic invasion of water must occur far quicker than ionic exchange since complete release of larvae does take place when female worms pass out into the redd along with the eggs of the fish and burst.

A comparison of the oncomiracidia of the monogenean skin parasites Entobdella hippoglossi from the halibut (Hippoglossus hippoglossus), E. diadema from the sting ray (Dasyatis pastinaca) and E. soleae from the skin of the common sole (Solea solea) has revealed the presence of ‘body gland cells’, all of which have openings on the ventral or lateral surfaces of the larvae. In all three species there are two pairs of glands lying in the posterior region of the body proper with long ducts extending into the haptor and opening on its ventral surface. In addition to these two pairs of glands there are seven other pairs of body glands in E. hippoglossi, six pairs in E. diadema and two pairs in E. soleae. In E. soleae all the ‘body gland cells’ are poorly developed in the oncomiracidium and are more conspicuous in post-oncomiracidia. The fate of the ‘body gland cells’ during post-oncomiracidial development has been studied in E. soleae, and their possible functions are discussed. The glands in the head region (anterior median, posterior median and lateral head glands) are similar in all three species. Gland cells associated with the alimentary system are less easy to observe but differences between the three species appear to be small.

In the oncomiracidia of all three species the number of flame cells and their distribution are the same, but the oncomiracidia of E. hippoglossi and E. diadema have loops in the excretory ducts anterior to the bladder and the bladders of E. diadema contain refringent bodies.

The oncomiracidial eyes of E. hippoglossi and E. soleae have lenses but the lenses are greatly reduced in the oncomiracidia of E. diadema. In the three larvae there are small but characteristic differences in the shapes of the accessory sclerites.

The oncomiracidium of E. hippoglossi has not previously been described.

By a variety of microscopical techniques, an initial survey has been made of the functional organization of ovarian balls from mature, inseminated female Moniliformis dubius and Polymorphus minutus. On the basis of evidence from observations made with the transmission electron microscope, we have concluded that the ovarian ball consists of three components; these are two separate, multinucleate syncytia and a cellular zone. The inner region is considered to be an oogonial syncytium from which the germ-line cells arise to form the cellular zone. The oogonial syncytium and the cellular elements are embedded in a supporting syncytium which also forms the boundary of the ovarian ball. Details of the ultrastructure of these components, observations on fertilization and a hypothesis to account for the main events occurring in an acanthocephalan ovarian ball are also presented.

Acanthocephalans are dioecious parasites which become sexually mature in the alimentary tract of vertebrates. After insemination, individual female worms begin to release embryonated eggs at rates which have been estimated to vary, on average, from 2000 per day in the case of Polymorphus minutus (Crompton & Whitfield, 1968) to 260000 per day in the case of Macracanthorhynchus hirudinaceus (Kates, 1944). Irrespective, however, of the species of acanthocephalan and the number of eggs produced, a most interesting mode of ovarian development and multiplication is believed to exist (see Bullock, 1969). Within the female worm, the primordial ovarian tissue gives rise to separate ovaries which are often termed ovarian balls. These in turn give rise to more ovarian balls and the process continues until large numbers have been formed. The ovarian balls of a mature female have no permanent attachment to the tissues of the worm. They are contained in the fluid of the body cavity either freely, or loosely constrained in large membranous chambers known as ligament sacs.

Few investigations have been made into the structure and cytology of the ovarian balls of the Acanthocephala. Early observations on the histology of the germ-line constituents of ovarian balls were made by Hamann (1891), Kaiser (1893) and Meyer (1928), each of whom suggested that some of the developing oogonial stages were arranged in a syncytial manner. In a study of the embryology of P. minutus. Nicholas & Hynes (1963) interpreted preparations of ovarian balls, which had been subjected to the Feulgen reaction, as indicative of syncytial tissue in the central region of the ball. They also recorded their uncertainty about whether an ovarian ball has a bounding membrane or not. More recently, Robinson (1964, 1965) described mitotic and meiotic divisions in oogonia and oocytes from ovarian balls of Mac. hirudinaceus and Moniliformis dubius and Stranack (1972) included an electron micrograph of part of an ovarian ball of Pomphorhynchus laevis in a description of the nature of the egg envelopes of that species. In this paper, we present a general survey, based largely on evidence obtained with the electron microscope, of the functional organization of the ovarian balls of mature M. dubius and P. minutus.

Milk-borne infection is demonstrated for Strongyloides ratti in rats, accounting for 32% of the combined worm burden of non-immune mothers plus their offspring at a standard dose of 4000 L3. Migrating larvae are ‘switched’ to the mammary gland about 3 days prepartum in advance of the final events of lactogenesis in the host at 30 h prepartum. Larvae take between 24–48 h to reach the milk after injection.

The ‘take’ in lactating rats was half that in virgin controls and pregnant animals before day 3 prepartum, but this discrepancy was not made up by the number of worms in the litter, the combined figure for mothers and offspring still being only 75% of the potential judged by the controls.

Prenatal infection did not occur in these experiments, which involved carefully controlled cross-fostering between infected and uninfected mothers. Injections of larvae covered the period between 12 days to 20 h prepartum in different animals. This route is possible under other circumstances, although it is considered unlikely in non-immune females since there was no evidence of larval dormancy in maternal tissue.