The clamp sclerites of Pricea multae and other higher monogeneans was fuchsin-positive in Mallory's and Masson's triple stain, and the staining was not affected by detanning agents, suggesting some form of stabilization in the protein. The sclerites were positive in Millon's, Morner's and Xanthoproteic tests for aromatic amino acids, but negative in tests for sulphydryl and disulphide groups. Quinone, phenol and phenol oxidase were absent. They stained with basic dyes such as toluidine blue and methylene blue in the pH range of 3·5–9·5, and also exhibited bluish fluorescence in u.v. light which was not affected by lipid solvents, indicating the presence of dityrosine and recalling the protein present in the ligament cuticle of insects. These features indicate that the clampprotein is stabilized by the formation of dityrosine. It is suggested that this protein may be responsible for the biological properties of the clamp sclerites. This mode of stabilization by tyrosyl residues of the protein, resulting in the formation of dityrosine, is the first record of its kind to be reported in platyhelminths.

The embryonic epithelium in Hymenolepis diminuta appears in the early preoncosphere stage. Inside the embryo there is a binucleate cell connected by a cytoplasmic strand with an epithelial layer spreading over the embryonic surface. After the embryo has become covered by tine epithelium the latter delammates into three layers. A basal layer resting on the basal lamina accumulates dense bodies. These bodies are spheroid and membrane-bound in the early embryo. In the late preoncosphere stage rodlike bodies remain in the basal epithelial layer. The basal membrane forms long invaginations into the basal layer. The intermediate epithelial layer is rich in polysomes and it is postulated that secretes extracellular material which cements the intermediate and peripheral layers and the ‘oncospheral membrane’. The continuity in embryonic, larval and adult cestode epithelium is discussed.

Hepatojarakus bandicoti sp.nov. has been described from Bandicota bengalensis (type host), Millardia meltada, Tatera indica and Mus musculus bactrianus. The genus Hepatojarakus Yeh, 1955, has been retained in the family Trichostrongylidae Leiper, 1912. This is the second record of Hepatojarakus and the first from India.

The immune reaction of larvae of D. algonquin against P. bochei was characterized either by the melanization and encapsulation of the parasites or by the production of melanized particles. In successful host reactions the eggs of the parasite were killed before they were completely melanized and encapsulated by haemocytes. When host larvae were transferred during the early stages of infection to a diet that contained phenylthiourea (PTU), the incidence of melanization and encapsulation of the parasites was significantly reduced. However, if the hosts were transferred to the diet just before the eggs of the parasite were normally melanized, PTU had virtually no inhibitory effect, and the immune reaction rate remained very high. These results suggest that the biochemical reactions associated with melanization constitute an important part of the immune reaction of D. algonquin. The data provide additional evidence to support the idea advanced by other workers that the phenoloxidase system plays an important role in insect immunity against some internal metazoan parasites. It is suggested that, during infection, the phenoloxidase system of the haemocytes is activated by hormonal imbalance.

The free pool amino acids of Taenia crassiceps metacestodes (advanced larvae) were analyzed quantitatively. In addition, the uptake of L-glutamic acid, L-proline, L-phenylalanine, L-lysine, and L-methionine was studied. Proline and glutamic acid absorption followed straight-line kinetics with respect to substrate concentration, and were not inhibited by their own molecular species. Lysine, phenylalanine and methionine were found to enter larvae by a combination of diffusion and mediated processes. Lysine absorption was inhibited only by lysine, arginine and ornithine. Phenylalanine and methionine uptake was not inhibited by lysine or arginine, but was inhibited by several other amino acids. The data suggested the presence of a basic amino acid transport locus and two distinct transport loci for methionine absorption. In addition, both immature and advanced larvae were found to be impermeable to [14C]inulin (M.W. ca. 5000). These results are discussed and compared with the results of earlier investigations of protein and amino acid absorption by T. crassiceps larvae.

The phenomenon of self-cure, as it occurred under field conditions in East Africa, was studied in Merino sheep infected with Haemonchus contortus. The onset of self-cure, as judged by a dramatic fall in faecal egg counts, was found to be simultaneous in sheep grazing on infected pasture and in sheep grazing on parasite-free pasture. Furthermore the results of autopsies carried out before and after self-cure showed that a marked and equal loss of adult worm burdens had also occurred. These results indicate that self-cure of H. contortus infections under natural conditions occurs in the absence of reinfection and is apparently non-immunological in origin. Since the phenomenon was always associated with a period of significant rainfall, it is suggested that new growth of pasture may be a significant aetiological factor.

A strain of E. tenella which had been passaged serially in 42 batches of chick embryos appeared to have lost its ability to produce the characteristically large second-generation schizonts in both the embryonic chorioallantois and in the chicken caeca. Numerous small schizonts (10–16 µm in diameter), which contained 8–30 small merozoites, replaced the large second-generation schizonts characteristic of this species. The small schizonts were numerous 3–5 days after inoculation and were restricted to epithelial cells of the embryo allantois when sporozoites were inoculated via the allantoic cavity. These schizonts also occurred in epithelial cells of the caeca of chickens given oocysts via the crop. Cell reactions in the chicken caeca in response to infection were minimal. Numerous minute lesions were present in the chorioallantois 4–6 days after inoculation; these were associated with the small schizonts and later with gamonts and oocysts. The strain reproduced well in the embryo but failed to induce gross pathogenic effects and no mortality resulted from the infection.

Only two passages of this strain in chickens were needed to restore a high degree of pathogenicity. This change was accompanied by the reappearance of the characteristically large second-generation schizonts in the tunica propria of the caecal wall.

Lobatostoma manteri sp.nov. is described. It differs from other species of this genus in the number of marginal alveoli (usually 56–62), the location of the testis near the posterior end and the large size of the cirrus pouch. Mature worms occur in the intestine of the fish Trachinotus blochi. Eggs containing fully developed larvae are laid. The eggs are eaten by snails and hatch in the stomach. Larvae have an oral sucker, pharynx, simple caecum, ventro-terminal acetabulum, two dorsal excretory bladder cells in front of the acetabulum, and a caudal appendage. They migrate into the digestive gland and differentiate to pre-adults with fully developed genital organs and the full number of alveoli on the adhesive disk; young spermatozoa and egg cells develop but do not mature. Pre-adults have a minimum number of 8500 sensory papillae on the surface. The worms are usually found in a cavity formed by enlargement of the main duct and one or more (?) side ducts of the digestive gland near the stomach in Cerithium moniliferum, or in the stomach and main ducts of the digestive gland of Peristernia australiensis. They may creep from the ducts into the stomach and back into the ducts. Fish become infected by eating snails. Worms from fish die soon after transfer into sea water but can be kept alive for up to 13 days in frog's Ringer solution or dilute sea water (1:5), in which they lay eggs containing larvae infective to snails. Worms from snails remain alive in sea water, dilute sea water, frog's Ringer or Tyrode solution. Eggs of worms from single infections have the haploid chromosome number of 7; there is normally no self-fertilization and development does not reach the blastula stage. The life-cycle of Lobatostoma manteri is the simplest two-host cycle of trematodes known. Reasons are given why it must be considered the most primitive one, of a type from which digenean life-cycles have evolved.

A comparison was made between 14-day-old populations of Nematodirus battus from single infections and from those which developed concurrently with Haemonchus contortus from the day of infection and from days 5 and 10 after infection. The numbers of Nematodirus fell with decreasing length of exposure to Haemonchus and were negatively correlated with the numbers of Haemonchus. The percentage of the populations of Nematodirus in the adult stage and the mean worm lengths fell with increasing length of development with Haemonchus, the lowest values being found in infections which developed concurrently with the abomasal worm for the full 14 days (days 0–14). Mean Nematodirus worm lengths were negatively related to abomasal pH and Na+ levels in populations which were concurrent with Haemonchus for the last 9 days (days 5–14) and for the full 14 days of development studied. Nematodirus egg capacity also fell with exposure to Haemonchus, but was lower in the worm populations exposed for the last 9 days than in those exposed for 14 days. Egg capacity was related to abomasal electrolyte levels in populations which had developed concurrently with Haemonchus for the last 9 days and for the full 14 days. Significant differences between the population parameters of Nematodirus from the proximal and middle third of the small intestine were only found in the single Nematodirus infections and in those which were concurrent with Haemonchus for the last 4 days (days 10–14). The differences in the populations of Nematodirus were related to the probable changes in alimentary conditions affected by the different periods of concurrent infections of Haemonchus. It was suggested that the alimentary changes may have caused the loss of adult Nematodirus and have influenced the growth, development and reproductive capacity of the intestinal worm by acting upon the fourthand fifth-stage larvae.

Possible relationships between the numbers and development and growth of Haemonchus contortus and Nematodirus battus during concurrent infections and the levels of abomasal pH and Na+ were investigated in 2- to 3-month-old and 8-month-old lambs. The percentage of Haemonchus in the fourth larval stage was found to be positively related to the levels of abomasal electrolytes, while the mean lengths of the worms in the total male and female populations and in the fifth-stage populations were negatively related to these parameters. The numbers of Nematodirus and the mean lengths of worms in the total and fifth-stage populations were negatively related and the percentage of worms in the fourth-stage positively related to abomasal pH and Na+ levels. It is suggested that the changes in abomasal physiology caused by massive infections of Haemonchus directly affect the growth and development of this abomasal parasite. It is also suggested that the changes in the abomasal contents entering the proximal part of the small intestine during such infections of Haemonchus alter the intestinal environment and that this alteration directly affects the course of development of concurrent infections of Nematodirus.

When the eggs of the skin parasitic monogenean Entobdella soleae are subjected in the laboratory to alternating periods of light and darkness (LD 12:12, LD 6:18 or LD 18:6) at constant temperature (selected from the range 12–16 °C), hatching is rhythmical, most of the oncomiracidia emerging during the first 4 h of the period of illumination on each successive day.

Rhythmicity in response to alternating 12 h periods of light and darkness persists in a wide range of lighting conditions including natural daylight and in dim blue light, the latter being similar in intensity (65 nW/cm2) and in spectral quality to light at the depths where the host Solea solea lives.

The hatching rhythm persists with a periodicity of about 24 h in constant darkness and in constant light, provided that the eggs have been exposed previously to LD 12:12 until hatching begins. This indicates that there is a strong endogenous component to the rhythm.

Eggs laid and maintained in total darkness develop and hatch, but the oncomiracidia may emerge at any time during each 24 h period and there is little evidence of rhythmicity.

When alternate 12 h periods of light and darkness are reversed after the commencement of hatching, the hatching pattern also reverses after 24 h, so that emergence of larvae occurs at the beginning of the new illumination period.

Mechanical disturbance plays little or no part as a hatching stimulus.

Larvae, which had emerged from their eggs at some time between 20 and 80 min previously, responded to host skin, suggesting that an initial uninfective period is of short duration or absent.

Hatching soon after dawn may have high survival value for E. soleae in view of the host's activity pattern; soles are active at night and partly bury themselves in the sediment (where the eggs of the parasite lie) at dawn, and the fish is inactive and a stationary target during the day.

The adults of Solenopotes tarandi (Mjöberg, 1915) are redescribed and illustrated, and its allied species of Solenopotes are compared. The nymphs of this species are for the first time described and illustrated. Ectoparasite infestation of the barren ground caribou (Rangifer tarandus granti Allen) is also discussed.

The adult of P. crucibulum is redescribed to form a basis for comparison with the cercaria and metacercaria. Particular emphasis is given to the structure and function of the rhynchus, digestive system and reproductive system. Some features, notably prepharyngeal glands and spematophores, have not previously been recorded in this species.

The sporocyst and cercaria which were found in Mytilus edulis are described for the first time. Out of 6907 mussels examined from Borth Rocks, Cardigan Bay, 0·26% were infected with P. crucibulum and 0·06 % with P. squamatus. The cercaria of the latter is redescribed on a comparative basis with that of P. crucibulum, to avoid confusion. The two cercariae are clearly distinguished by three features – flame-cell formula, shape of the excretory vesicle, and structure of the tail stem (this being bilobed in P. crucibulum and trilobed in P. squamatus). The significance of the two types of tail in securing attachment to the second intermediate host is discussed.

Metacercariae of P. crucibulum were obtained experimentally in ‘O’ group specimens of Scophthalmus maximus. Three other species of fish, namely Limanda limanda, Onus mustelus and Gobius minutus were also successfully infected. The metacercariae did not develop in the following fish: S. rhombus, Pleuronectes platessa, Cottus bubalis and Blennius pholis. Possible mechanisms which might account for host specificity within Pleuronectidae and Scophthalmus are suggested.

The development of the metacercaria in the connective tissues and musculature of S. maximus was followed over a period of 10 months. Within 1 month of infection the hyaline cyst of parasitic origin breaks down, enabling the parasite to feed directly on the host tissues. This feature is thought to account for the advanced development of the metacercaria, which 1 month after infection could clearly be identified with the adult on the basis of comparative morphology, and at 2 months resembles the adult in every respect except the development of the vitellaria. Egg production only occurs within the intestine of Conger conger, the definitive host.

Regions have been identified in certain oxyuroid nematodes which stain vitally with quinone-imine dyes. Thelastoma attenuatum shows colour in the arcade cells, the small pseudocoelomocytes and the giant pseudocoelomocytes; while Leidynema appendiculata and Hammerschmidtiella diesingi possess only giant pseudocoelomocytes. All these regions have been studied.

The giant pseudocoelomocytes in all three species are apparently very active, but their precise function had not yet been assessed.

The structure of the arcade cells and small pseudocoelomocytes of Thelastoma have been described. These regions may also be active but their function is again not understood.

Further work to elucidate these problems is suggested.

Mice infected with as few as ten eggs of the nematode Trichuris muris are highly resistant to a challenge infection given 5 weeks later. The rate of elimination of challenge larvae is similar in mice immunized by infection with ten or with 300 eggs. Stimulation of immunity to challenge by the low-level infections is dependent upon the persistence of the immunizing worm population and removal of the population at day 14 considerably reduces the level of immunity. Worms developing from a low-level immunizing infection are not eliminated by a ‘self-cure’ response, as is the case with larger infections, and become sexually mature. Adult worms from such an infection are, however, eliminated by the response to a superimposed challenge infection. Repeated infection of mice with small numbers of eggs stimulates an immune response and the worm population is eliminated before patency.

The efficiency of assimilation of carbon and nitrogen by Littorina saxatilis, as calculated from the carbon and nitrogen content of food and faeces, showed that the efficiency of snails infected with rediae of Cryptocotyle lingua did not differ significantly from that in non-infected snails.

Similarly, the rate of ingestion and the rate of assimilation of infected snails did not differ significantly from those of non-infected snails.

It is suggested that this harmonious relationship reflects the longterm strategy of Cryptocotyle lingua infections.

The structure of H. placei adult worms, obtained from calves at 4, 7, 10 or 11–13 weeks after primary infection, has been studied. A reorganization of rough endoplasmic reticuhim in the cytoplasm of the gut cells was seen at 10 weeks and this was followed by marked vacuolation of many of these cells, associated with an increase in lipid production. Increases of lipid were also found in the hypodermis, lateral cords and occasionally muscle cells of worms examined at 11–13 weeks after infection.

It is suggested that these changes are the result of the host immune response, because they resemble changes which occur in the rat nematode Nippostrongylus brasiliensis and which are known to be caused by host immunity.

The junction between the gregarine trophozoite Nematocystis magna Schmidt and an epithelial cell of its earthworm host Lumbricus terrestris Muller consists of an extensive folding and meshing of the single trilaminar membrane bounding the host cell and the complex folded multilaminar limiting membrane of the trophozoite. They are separated by a structureless intercellular region of some 50 nm in width. Specialized communicating regions or permeable elements were not observed. Transport of a radioactive label across non-junctional and junctional membranes was demonstrated by using tritiated glucose. The attachment organelle of the trophozoite is shown to be capable of allowing metabolites to pass into the cell directly from the host tissue.

Trypanosoma bouffardi Leger & Blanchard, 1911, is described from naturally infected Lagonosticta s. senegala, Estrilda b. bengalus, Vidua chalybeata, Estrilda t. troglodytes and Amadina f. fasciata, all of which are new host records for Nigeria; Vidua chalybeata is a new host record for trypanosomes.

There was no significant morphological difference between populations of this trypanosome in the various natural and experimental vertebrate hosts.

T. bouffardi was transmissible to nine species of Ploceidae belonging to the three subfamilies Estrilinae, Ploceinae and Viduinae; but not to Pycnonotus barbatus, chickens or pigeons.

The parasitaemia produced by infections of T. bouffardi reached 4·1 × 105 parasites/mm3 of blood.

Reproduction of the trypanosomes was synchronous and discontinuous and occurred in the blood by unequal binary fission of trypomastigotes. Occasionally longitudinal equal binary fission of trypomastigotes also took place. There was no concentration of dividing forms in the tissues.

T. bouffardi did not grow on NNN medium although it has been grown for a short time on the medium described by Yesufu (1970).