Glycogen reserves of whole worms and their body wall, intestines, ovarian and testicular tubules of the avian intestinal nematode, Ascaridia galli, were assayed and on dry-weight basis found to be 14–20 %, except in the testicular tissue which contained only 7 % glycogen.

Segments of whole male worms or testicular tubules were found to produce more lactic acid than segments of whole female worms or ovarian tubules. The body wall and intestine of the worms had also appreciable glycolytic activity. Whereas in the segments of whole worms, male and female alike, glycolysis was more active under anaerobic conditions, no differences in glycolytic rates were seen between aerobiosis and anaerobiosis when isolated tissues were used. Exogenously added glucose did not stimulate glycolysis either aerobically or anaerobically to any extent greater than observed in the absence of glucose.

Homogenates of whole worms or their different anatomical parts were assayed for enzymic activities associated with the Embden-Meyerhof pathway of glucose assimilation. The crude extracts prior to differential centrifugation, were found to contain glycogen phosphorylase, aldokinases, pyruvate kinase, phosphatases acting on glucose 6-phosphate and hexose diphosphate and 6-phospho-gluconate dehydrogenase. The 105000 g particulate-free supernate was found to have significant activities of the following enzymes: fructokinase, phosphoglucomutase, phosphoglucoseisomerase, phosphofructokinase, aldolase, glyceraldehyde 3-phosphate dehydrogenase, lactic dehydrogenase and glucose-6-phosphate dehydrogenase. This fraction was devoid of NADH or NADPH oxidase activities in the absence of added substrates.

Although there was some indication of a negative correlation between low glycogen reserves and high glycolytic activity in the testicular tubules, in general, there was no relationship between glycogen reserve and glycolytic activity on the one hand or between the rate of glycolysis and the specific activities of some of the key glycolytic enzymes in either whole worm or in tissues other than the testicular tubules.

The 105000 g supernate was fractionated with ammonium sulphate. The fraction precipitating between 25 and 80 % saturation of the salt was recovered, dialysed and chromatographed on DEAE cellulose column. By a step-wise elution schedule using increasing molarity of NaCl in tris-HCl buffer, pH 7·4, three main protein fractions were obtained representing respectively enolase, aldolase and glucose-6-phosphate dehydrogenase.

The recovery of enzyme activity after chromatography on DEAE cellulose was higher than the amount applied to the column suggesting that during the fractionation some naturally occurring inhibitors were removed. About 10- to 20-fold purification of the enzymes was achieved by anion-exchange chromatography.

Some properties of the purified enzymes were studied with respect to the affects of enzyme and substrate concentrations, temperature of preincubation and action of divalent cations, some anions, metal chelating agents and SH reagents. The Km values of enolase, aldolase and glucose-6-phosphate dehydrogenase of A. galli were 5·9 × 10−4M, 4·5 × 10−3M and 2·4 × 10−3M respectively. Glucose-6-phosphate dehydrogenase was found to be very sensitive to both heat and cold losing activity rapidly even at 43 °C or by freezing and thawing.

The SH groups of aldolase were readily blocked by pCMB and presumably by o–phenanthroline. No requirement of any divalent cations was shown by this enzyme which was, however, inhibited by borate ions.

Enolase of A. galli showed a requirement of Mg2+ for full activation. Phosphate, fluoride, EDTA, o–phenanthroline, αα-bipyridyl inhibited the enzyme. Veronal was found to inactivate the enzyme.

Glucose-6-phosphate dehydrogenase of A. galli was also found to be sensitive to SH reagents and metal chelating agents. The enzyme was activated by Co2+, Mn2+ and Mg2+.

The evidence presented indicates that segments of whole worms of A. galli or its anatomical parts are equipped with the enzymatic machinery required to mediate anaerobic breakdown of glucose and to derive energy by this mechanism.

The authors are grateful to Dr R. K. Kaushik for help in identifying the worms, to Mr P. A. George for help in the statistical analysis of the data and to Messrs A. C. Kol and S. K. Bose for skilful technical assistance.

The intimate cell relationships of Hymenolepis diminuta are described and occur between cells of the parenchyma, excretory system, muscle and tegument. The cell relationships are of three types: (a) a tight junction or zonula occludens; (b) a desmosome-like structure without tonofibrils or intercellular dense line; (c) a junctional complex with modified unit membranes and an intercellular region of dense granules and fibres.

This research was begun while one of us (L.T.T.) was a Visiting Lecturer in the Biology Department, Rice University, and completed in the Zoology Department, Queen's University, Belfast. We should like to thank Dr C. W. Philpott for allowing us the full use of the facilities of his electron-microscope unit and Mr W. Ferguson for photographic assistance.

Adult Hymenolepis diminuta were tested for their ability to transport colloids under in vitro and in vivo conditions. The tracers employed included colloidal thorium dioxide (Thorotrast), carbon (Pelikan Ink), ferritin and the 14C-labelled protein fraction from Chlorella vulgaris. Though certain of these tracers were adsorbed to the external surface of the tegument plasmalemma, no evidence for the assimilation of any of these colloids was obtained in the present study. Further, significant differences in size and structure between the granular inclusions reported earlier by Rothman (1967) as assimilated colloids and the particles present in the respective colloidal suspensions were noted. Results of this investigation are interpreted as rendering untenable previous conclusions concerning transmembranosis of colloids by tapeworms.

Of 414 Bermuda fishes, 148 belonging to 13 species harboured Digenea and 11 belonging to 6 species Aspidogastrea, Acanthocephala or nematodes. In a previous paper 69 of these fishes belonging to 20 species were found to contain cestodes. The number of infected species was greatest in the case of cestodes and the number of infected individuals in the case of Digenea. The latter is probably due to the closer proximity, for reasonably long periods, of the various hosts in the life-cycles. Of the 17 species of Digenea 3 are new host records, 3 new locality records and 4 new host and new locality records. New records were found, also, in the other groups of helminths. The digenean fauna of Bermuda fishes most closely resembles that of Dry Tortugas, Florida. Digenea and cestodes were not usually found in the same families of fishes. Cestode larvae were abundant in the deep-water Serranidae and Lutianidae which had no Digenea, the latter being common in Clupeidae, Hae-mulidae and Belonidae, which do not harbour cestodes and which occur, mostly, in the inner reefs and shallows.

The functional morphology of the apical disk, tentacles and rhynchus of Alcicornis carangis is described. The tentacles are invaginable and concerned with attachment.

I am most grateful to Dr W. H. Sutcliffe Jun., Director of the Bermuda Biological Station, for the excellent facilities provided and to The Shell Grants Committee and The National Science Foundation for grants which made the work possible. I would also like to express my gratitude to all those who kindly helped in the capture of fishes and to Mrs M. Fisher for technical assistance.

The results of ultrastructural studies and histochemical tests on the capsule of Trichinella spiralis are given. The capsule wall is shown to consist of two layers, an outer region of tightly compacted fibrils and an inner region of fibrils dispersed through matrix cytoplasm. Histochemical tests show the capsule wall to consist mainly of collagen and cystine. The appearance of the matrix, which is packed with mitochondria, rough endoplasmic reticulum, smooth reticulum and Golgi complexes, together with the histochemical reaction to the five enzymes tested, strongly suggests that the matrix is a region of high metabolic activity. Although there are several very large nuclei in the matrix there is no evidence of cell walls; consequently the matrix is a syncytium.

I wish to thank the A.R.C. for financial support while this work was carried out. I should also like to thank Dr D. L. Lee for his advice on many occasions and the late Professor Boyd of the Anatomy Department, University of Cambridge, for the use of the electron microscope in that Department.

Cortisone acetate, given to mice on two days during a primary infection with the nematode Trichuris muris, suppressed the development of acquired immunity to the parasite. The proportion of mice in which suppression occurred was greatest when the drug was given (at 2.5 mg per mouse) on days 14 and 15 of the infection. Suppression of the response prevented the elimination of larvae, which otherwise occurs during the third week, and allowed the parasite population to mature and survive for at least a further 3 weeks. Similar treatment given during a challenge infection in resistant mice prevented the elimination of the challenge larvae for 2 or 3 days only. Mice in which cortisone treatment had prevented the elimination of a primary infection were not only found to be fully susceptible to subsequent challenge, but showed no development of immunity to the challenge infection itself. This long-lasting suppression of the immune response to T. muris is discussed and the possibility of the induction of a specific immunological unresponsiveness to the parasite is considered.

An analysis of natural infections of Toxocara mackerrasae in Rattus fuscipes trapped in rain forests in south-eastern Queensland is given and Hydromys chrysogaster is listed as a new host.

T. mackerrasae larvae in egg-infected mice are incapable of somatic migration but some complete development to the young adult stage can occur entirely within the alimentary tract. T. mackerrasae is capable, in low numbers, of developing to maturity in experimentally infected Rattus spp.

The work was financed by grants from the University of Queensland and the National Health and Medical Research Council of Australia. I wish to thank Professor J. F. A. Sprent for his criticisms and suggestions during the preparation of this text.

Following a 2–5 ml meal containing 2 g (80%) glucose and 30 mg methionine administered by stomach tube at 09.00 h, H. diminuta was found to change its position in the rat's intestine. Usually while the stomach contained food ≤ 45 %, by weight, of the tapeworm lay in the posterior 40 % of the small intestine, after the stomach was empty the reverse was true.

The effect of hyperosmotic fluid entering the duodenum was determined by injecting, following laparotomy, varying amounts of 80 % glucose and 1 ml of varying concentrations. A volume ≤ 0-4 ml of 80 % led to the death and expulsion of worms within 7 h, and 1 ml of < 50 % glucose also killed the worms.

The expulsion of 15 % of the tapeworms from rats given 2–5 ml hypertonic meal by mouth was correlated with the failure of the stomach in some rats to regulate the stomach emptying. Worms in these rats were found from 4 h onwards in the caecum and large intestine, and by 9 h in the faeces.

That the movement of worms, other than those expelled, was not caused by a sub-lethal flux of hyperosmotic fluid was shown by feeding an iso-osmotic meal to rats; the worms moved to a more posterior position during the day, but none was expelled.

Single worm infections in rats kept on a normal feeding regime until 07.00 h and then starved throughout the day also showed a posterior migration. Using a method which involved the simultaneous cutting of the small intestine into 5 cm sections, it was possible to show that this movement involved the whole worm, the scolex moving from a mean position 10–15 cm to one 20–25 cm from the stomach, and the terminal proglottid moving from approximately 75 cm to 95 cm from the stomach.

Worms in Wistar rats responded similarly to those in SPF CFE (Sprague Dawleys) with the exception that there was some evidence that the stomach emptying of a hyperosmotic meal was better controlled and hence a smaller percentage of the worms were expelled.

The results are discussed in relation to diurnal changes in the level of the external site location stimulus which other workers have shown to exist by surgically transplanting H. diminuta into the ileum.

The enthusiastic assistance of Miss Helen Stallard, B.Sc., and Miss Patricia Grant is gratefully acknowledged, and financial support from the Medical Research Council, London (Grant No. G967/164/T).

A study has been made of the parenchyma of adult male Schistosoma mansoni by electron microscopy. Four different cell types have been characterized: one corresponding to cell bodies of the integument, two to muscle cells and another one to nerve cells with a possible neurosecretory function. The cytoplasm of the integument cell bodies is characterized by rod-shaped and round membrane-bound cytoplasmic bodies with a dense core, measuring 1200 to 2000 Å, similar to those found in the integument. One type of muscle cell has a large, clear nucleus, characteristic cytoplasmic vacuoles measuring up to 1 μm with a finely granular content and numerous free ribosomes. The other type of muscle cell is much smaller, with clumped nuclear chromatin and scanty perinuclear cytoplasm. Both types of cells give rise to muscle fibres which are morphologically distinct from the perinuclear cytoplasm. The nerve cells contain electron-dense, membrane-bound vesicles-ranging in size from 1000 to 3000 Å, similar to those found in nerve axons.

Appreciable extracellular matrix has only been found under the integument and surrounding the processes of the integument cell bodies. This observation and the fact that silver methenamine after periodic oxidation stains intensely both the extracellular substance and the rod-shaped and round cytoplasmic bodies of the integument cells, suggests that these integument cells may be involve the production of extracellular matrix.

This investigation was supported by grant AI 07806 from the U.S.P.H.S.

The technical assistance of Mrs Lucille Jeffries and the photographic assistance of Mr William Douglas are acknowledged. This investigation was supported by the United States–Japan Cooperative Medical Science Program administered by the National Institute of Allergy and Infectious Diseases of the National Institutes of Health, Department of Health, Education and Welfare.

Estimates were made of the intake of strongyloid infective larvae by sheep at pasture by the recovery of larvae from samples of herbage collected through oesophageal fistulae.

All herbage eaten was not recovered through the fistula but few larvae were lost in the process of mastication and swallowing. More larvae could be recovered from macerated than from undamaged herbage.

Samples were obtained from different sheep on different days and at different times during the day and the variance components associated with these factors were estimated from seven sets of observations. The contribution to variance differed widely for each factor with the major contribution coming from time changes in the differences between sheep.

The authors wish to thank Mr G. W. Major for valuable technical assistance throughout these studies.

Surgical bursectomy or thymectomy at day old had little effect on primary or subsequent infections with E. brunetti or E. maxima.

Whole body irradiation of day-old chickens with 700 or 750 R did not affect the development of immunity to these Eimeria spp., but in some experiments it affected oocyst production during initial infections.

In one of four trials, birds surgically bursectomized and irradiated produced twice as many E. brunetti oocysts during an initial infection as the irradiated only controls; in the remaining three trials, oocyst production in the operated birds was either similar to or slightly greater than that in the controls. Combined bursectomy and irradiation did not affect immunity to re-infection.

Combined thymectomy and irradiation had little effect on primary infections (increased oocyst output was found in only one of six trials) and no effect on subsequent immunity; mean body weights and circulating lymphocyte numbers were decreased but tuberculin sensitivity was reduced in only a small proportion of the birds, indicating that the cell mediated immune responses of the majority were not affected.

Small (0.75 mg) daily doses of cortisone acetate given to irradiated birds or irradiated thymectomized birds, did not affect resistance to reinfection with E. brunetti.

We wish to thank Dr B. M. Freeman for surgical bursectomy; Mr E. A. King, Department of Radiotherapeutics, University of Cambridge, for irradiation and members of the technical staff of the Parasitology Department for their willing and skilled assistance.

It has been shown that mating involving mutual exchange of spermatophores takes place in the skin-parasitic monogenean Entobdella soleae from Solea solea. The spermatophores are attached to the ventral surface of the body in the region of the vaginal opening and they are sucked into the vagina after mating by muscular contractions of the vaginal region.

Mating takes place between young individuals with no vitellaria and between fully mature egg-laying adults but there is no evidence that self-fertilization takes place.

The apparatus which manufactures the spermatophores is described and the evidence indicates that spermatozoa are injected into the jelly-like matrix of the spermatophore as the matrix is being extruded into the surrounding sea-water.

I would like to thank the Director and Staff of the Laboratory of the Marine Biological Association at Plymouth for providing excellent facilities for this work and I am particularly grateful to Mr J. E. Green, who kindly fed and maintained infected soles at the Laboratory.

Filariids of birds of Taiwan, Palawan and Sabah are discussed. Oceanifilaria verrucosa gen. et. sp.nov. from woodpeckers is proposed in Dicheilonematinae. It differs from other genera in the subfamily in having asymmetrical caudal alae, in lacking sessile papillae between the alae and in possessing a band of cuticular bosses at the anterior end followed by a bare zone, the latter followed by irregular bosses over the rest of the body. Aprocta calliderma sp.nov. from a cuckoo differs from A. papillosa Chabaud, Anderson & Brygoo, 1959, in having an oesophagus about one-sixth as long. Parornithofilaria hepatica sp.nov. from a pigeon differs from P. lienalis (Orloff, 1947) Sonin, 1965, in having unequal spicules with the right 110–120 mm and the left 140–175 μm long. Parornithofilaria sonini sp.nov. from magpies differs from P. hepatica in spicule shape, tail length and distribution of caudal papillae. Other species reported and briefly discussed are: Hamato-spiculum quadridens (Molin, 1858) Boulenger, 1928, H. cylindricum (Zeder, 1803) Hartwich, 1954; Aprocta lepidogrammi (Tubangui & Masiluñgan, 1937) Anderson & Chabaud, 1958; A. cylindrica Linstow, 1883; Pseudaprocta decorata Li, 1933; P. gubernacularia Schikhobolova, 1930; P. sichoealinensis Oshmarin & Belous, 1951; Paraprocta brevicauda (Chandler, 1924) Maplestone, 1931; Paronchocerca tonkinensis (Chow, 1939) Lopez-Neyra, 1947; Diplotriaena corrugata Wehr, 1930; D. epsilon Johnston & Mawson, 1940; D. henryi Blanc, 1919; D. leiperi Anderson, 1959; D. ozouxi (Railliet & Henry, 1909) Henry & Ozoux, 1909; D. pungens (Schneider, 1866) Henry & Ozoux, 1909; and D. unguiculata (Rudolphi, 1819) Li, 1933.

We wish to acknowledge the field support by Dr D. S. Rabor, Department of Biology, Silliman University, Dumaguete City, Negros Oriental, Republic of the Philippines, and the technicians of the Parasitology Department of Naval Medical Research Unit No. 2 for general assistance in procurement and examination of hosts. Dr B. J. Myers assisted with initial handling of the specimens.