ALBERT

Notes: A method of delineating the extent of floods has been devised involving the establishment of flood surfaces and the creation of photogrammetric digital terrain models. These two data sources are combined in a computer aided map production system and comparisons are drawn between the efficacy of different forms of terrain modelling in a floodplain environment.〈section xml:id="abs1-2"〉〈title type="main"〉RésuméOn a mis au point, en vue de déterminer l'étendue d'innondations, une méthode numérique combinant les notions de surface innondable et de modèle numérique de terrain (MNT); on se pose le problème du choix du MNT dans un environnement de plaine innondable.〈section xml:id="abs1-3"〉〈title type="main"〉ZusammenfassungAngabe eines Verfahrens zur Ableitung der Ausdehnung von Überschwemmungen, wobei die Flut-Oberfläche bestimmt und photogrammetrisch digitale Geländemodelle erzeugt werden. Diese beiden Datenquellen werden in einem rechnergestützten Kartiersystem kombiniert, und es werden Vergleiche bezüglich der Wirksamkeit verschiedener Verfahren der Geländemodellierung in Flussniederungen gezogen.

Notes: SYNOPSIS. Ten new species of colorless Eugleninae are described. One of them is the type of a new genus (Calycimonas physaloides nov. gen. nov. sp.). Especially remarkable forms are: Astasia acus, a species related to the green Euglena acus but without chromatophores and stigma and considerably smaller; Astasia edax, a species with animal-like nutrition and peculiar ecological adaptations; Petalomonas striata, a form which is not spirally but transversely striated; and finally Hyalophacus caecus, which was observed already by Klebs and Pochmann but was not sufficiently described. The new genus Calycimonas (ex fam. Peranemacearum) is related to Tropidoscyphus on the one hand (nearly the same shape as e.g. Tr. octocostatus, but possessing only a single flagellum) and to Petalomonas on the other hand (mode of nutrition and of swimming, formation of the reservoir, rigidity: however in transverse section not flattened).The Astasiae with zootrophic nutrition are collected in a new subgenus Astasiae devorantes or Phytophaga which comprises besides A. edax three species already described by Skuja.

Notes: SYNOPSIS. H. canis (James) is reported from three of 36 stray dogs at Singapore and one of 34 palm civets (Paradoxurus hermaphroditus Pallas) from Jeram, Selangor. H. muris (Balfour) was found at Singapore in 10 of 61 examples of Rattus norvegicus (Erxleben) and five of 23 of R. rattus diardi (Jentinck), and is also recorded from six of 139 examples of R. r. jarak (Bonhote) from Pulau Jarak, Straits of Malacca. Neutrophils of P. hermaphroditus containing gametocytes of H. canis exhibit pronounced karyorrhexis, while most of the parasites themselves show signs of pyknosis.

Notes: SYNOPSIS. A total of 155 clones of Stylonychia putrina collected in nature were tested for mating type. Two sexually isolated varieties were found among them: Variety I with 12 mating types and Var. II with 11. Five of the clones isolated in the laboratory belonged to 3 additional mating types of Var. I making a total of 15 mating types in this variety.Crosses were made among 6 of the mating types of Var. I, and 114 clones of progeny were raised and tested for mating type. No simple genetic explanation of the results was evident.An abnormal type of conjugation with fusion of the conjugants and subsequent fission was studied. Both parental mating types sometimes segregated during the first two fissions of a fused animal. Mating type determination in the progeny of the fused animals seemed to parallel that of the progeny of the normal conjugants in that in both cases certain mating types tended to be dominant over others.

Notes: SYNOPSIS. The cytochemical procedure of Sen was used to demonstrate urease activity in Tetrahymena pyriformis S.

Notes: SYNOPSIS. The chimpanzee is shown to behave like man to infection with Babesia divergens or bovis: the intact animal is totally resistant, whereas the splenectomized animal develops a fulminating infection accompanied by blackwater. The splenectomized rhesus monkey reacts in the same way also, but splenectomized rabbits are insusceptible. In the chimpanzee the typical accolé position of the “divergens” organisms (as seen in cattle) is absent, but occurs in the rhesus. It is suggested that latent piroplasmosis in man may exist on a large scale in rural populations in infected localities.

Notes: SYNOPSIS. Studies cf 3 conjugating strains of Tetrahymena pyriformis grown in a bacterized medium indicated the presence of a system of alternative immobilizing surface antigens. Each strain was found to have the potential for the expression of 3 serologically unrelated antigens. These consisted of a “high temperature” antigen (expressed in the range of 20–35d̀C), a “low temperature” antigen (exhibited in cultures at 10d̀), and an antigen induced by growth in the presence of the above-mentioned “high temperature” antiserum. Normally, by the immobilization reaction, only one of these antigens could be detected as present on any one organism at any given time. The “high temperature” antigens of two of the strains were serclogically related while that of the 3rd strain did not cross-react with antisera to the other two. The “low temperature” antigens of the 3 strains were serologically related as were the antigens induced by growth in antiserum.Studies of inbred hybrids of two of the strains indicated a potential for still more alternative antigens as well as for the spontaneous expression of the antigen which in the parental strains could only be induced to appear by the presence of the specific antiserum.Study of the 3 strains in axenic medium indicated the existence of a more complex system and the possibility that two or more immobilizing antigens may be present simultaneously.

Notes: SYNOPSIS. The establishment of Eimeria tenella sporozoites in the cecal mucosa of the chicken is described. The invasion process was similar to that reported for E. necatrix by Van Doorninck and Becker. Sporozoites were found to pass through the surface epithelium of the cecal mucosa into the lamina propria. Within the lamina propria the sporozoites were engulfed by macrophages and transported to the cells of the glands of Lieberkühn. Development of the sporozoites ensues within the gland epithelium.

Notes: SYNOPSIS. The morphology of the vegetative phase and the sexual process in Pandorina morum have been studied in detail under controlled laboratory conditions. A number of strains from various areas of the United States, all essentially indistinguishable on morphological grounds, were analyzed for sexual compatibility. Forty-seven heterothallic clones were found to represent 15 separate pairs of mating types, or a minimum of 15 syngens (sensu Sonneborn, 1957). Two clones proved to be homothallic. Nine additional clones, which were not observed to mate with any strain, can be classified only after further collecting. The separate heterothallic pairs of mating types are sexually isolated by factors acting at the stage of gamete production; incompatible mating types produce no gametes when they are mixed together. The geographical distribution of the sets of mating types is very incompletely defined as yet, but they are not strictly endemic forms. Thirty heterothallic strains, representing each of the 15 sexually isolated sets of mating types of Pandorina morum, have been deposited with the Culture Collection of Algae maintained at Indiana University, Bloomington, Indiana, U.S.A.

Notes: SYNOPSIS. When grown in CPLM medium or in a similar medium containing glucose instead of maltose as its sugar, Tritrichomonas foetus, Strain O, was much more sensitive to injury when frozen to -21d̀ C. in the presence. of 1 m glycerol during the initial and logarithmic phases of its population growth curve than at its peak and for some time thereafter. In 7 experiments in which the population peak occurred an average of 28.1 hours after inoculation, the average culture age at which the protozoa first survived freezing was 20.3 hours, at which time the population had reached 52.6% of its peak. The optimum culture age for survival after 1 day of freezing averaged 37.7 hours at which time the population averaged 75.6% of its peak. The optimum culture age for survival after 7 to 15 days of freezing averaged 32.3 hours, at which time the population averaged 82.7% of its peak. Better survival upon freezing was obtained in those experiments in which the population peak was reached relatively rapidly.

Notes: SYNOPSIS. Specimens of Blepharisma undulans were transferred from young clone cultures to a rotocompressor with 3 mm3 of culture medium. The organisms were slightly compressed and photographed at various intervals with dark field illumination. The sequence of macronuclear and cytoplasmic changes was compared with similarly followed Feulgen preparations.The cycle falls into several phases: (1) an interphase (12–24 hr.) in which the organism increases in size while cytoplasmic and macronuclear appearances remain unchanged. During this phase, the macronucleus consists of 3 to 5 nodes of various sizes connected by strands. (2) a pre-condensation phase (1 hr.) in which a new posterior peristome and cytopyge appear without visible macronuclear change. (3) a condensation phase (10–20 min.) in which the macronuclear nodes coalesce into a round mass without dissolution of the central nodes or strands. (4) a postcondensation phase (1 hr.) characterized by: (a) elongation of the condensed macronucleus into a rod-like shape followed by typical nodal formation; or (b) elongation of the condensed macronucleus into a form resembling the letter “J”, followed by nodal formation, and resulting in a double row of nodes in one daughter and a single row in the other. Separation occurs at this time, initiating the new interphase. The development of the j-form macronucleus. the lack of obliteration of the central nodes, and the characteristic interphase condition distinguish this strain of B. undulans from others described elsewhere.

Notes: SYNOPSIS. Six species of astomatous Infusoria, 4 new, are described from the alimentary tract of Oligochaeta from Ochrida Lake. Two belong to Ochridanus, characterized by a cytoskeleton whose “V”-shaped basal piece bears on its branches two articulated hooks brought together by a skeletal blade. This genus found in Ochridanous Tubificidae represents the counterpart of Anthonyella in the Lumbriculidae of Lake Baïkal. The presence of Ochridanus in these worms concurs with the almost complete absence of representatives of Radiophrya of which we have found but one species. A species of Metaradiophrya, a genus unknown to date from the Lumbricidae, was noticed in Glossoscolecidae. The different species of Ochridanus, Anthonyella, Metaradiophrya, and Radiophrya compose a very homogeneous group of Radiophryinae. The study of the ciliary rows and the cytoskeleton of 2 species of Juxtaradiophrya, parasitic in the Lumbriculidae of Ochrida, shows that, in the morphology of these ciliates, as well as in the same forms from Lake Baïkal, many transition characteristics exist between the Radiophryinae and Hoplitophryinae or Mesnilellinae. These 3 sub-families, with their undeniable genetic kinship give coherence to the family Hoplitophryidae.

Notes: SYNOPSIS. Histochemical techniques were used to demonstrate the intracellular distribution of some hydrases, hydrolases, oxidases, and dehydrogenases in Stylonychia pustulata. The hydrase, aconitase, was confined to the mitochondria. Zymohexase activity occurred in the cytoplasm and probably in the mitochondria. The hydrolases, acid and alkaline phosphatases, lipase, and urease, were localized in the mitochondria. Lactic and glutamic dehydrogenases were confined to the mitochondria. Peroxidase and glycerophosphate dehydrogenase were absent.

Notes: SUMMARY. The mating behavior of 16 stocks of Paramecium multimicronucleatum from 12 states has been studied. Mating always follows a decline in nutritive conditions. The evidence indicates that there exists one set of four interbreeding mating types. The period of subculture strongly influences the mating reactions, many stocks mating only long after isolation from nature and culture in the laboratory under the restricted conditions employed. Selfing was observed to occur in many races, usually after long periods of subculture. It first occurred in only a small proportion of the population, later in a larger proportion. The similarities and differences between P. multimicronucleatum and other species of protozoa showing multiple mating types are discussed.

Notes: SUMMARY. A study of the temperature-pressure relationship in oxygen poisoning of Paramecium caudatum was undertaken, as the initial step in defining some of the major factors in in vivo oxygen poisoning. Paramecium was selected because it was relatively simple to culture in a pureline clone, large numbers were readily obtained, and it was large enough to be clearly visible under low magnification. The protozoa were exposed to oxygen pressures of 0 (100%), 15, 30, 45, 60, 75, 90, 105, 120 pounds/inch2 gauge pressure at each of the following temperatures: 1, 5, 10, 15, 20, and 27°C. Exposure was accomplished in a transparent, high-pressure lucite tank which permitted visual observation with aid of a dissecting microscope. It was found at temperatures above 5°C. that oxygen toxicity varied directly with pressure, but below this temperature, with oxygen tensions of 1–2 atmospheres (absolute), oxygen toxicity varied inversely as the temperature. The possibility is advanced that oxygen may be affecting two cellular processes (perhaps enzymatic), one of which is temperature-limited below 5°C. and would, therefore, decrease the death time as the temperature is decreased. Several experiments performed at 3°C. produced a death time intermediate between results obtained at 1° and 5°C.

Notes: SUMMARY. A stock of Paramecium bursaria is described in which the peniculus contains only 8 columns of cilia and associated “granules”. The gullet system is composed of organelle complexes almost exclusively, and incorporates no underlying or transecting extensions of “pellicular fibrillar systems”. A brief discussion is presented on the value of the peniculus as a taxonomic criterion in separating “aurelia” and “bursaria” groups in Paramecium.

Notes: SUMMARY. Strains E, S and W of Tetrahymena pyriformis were examined for their ability to carry out the reactions of the Krebs-Henseleit urea cycle, using growth and enzyme studies. None of the strains was able to grow on either citruliine or ornithine in place of arginine, and proline was as active as citrulline or ornithine in sparing arginine. So little citrulline or arginine was synthesized by cell-free preparations as to be of no significance in the growth or nitrogen metabolism of the ciliates. Slight arginase activity could be detected in homogenates, but no urea was found in cultures. No urease activity could be detected using urea-C14.

Notes: SUMMARY. An eimerian coccidian is described from the flying squirrel, Glaucomys volans, in Florida. It is identified as the same eimerian described by Roudabush from the flying squirrel in Iowa as Eimeria sciurorum. Evidence is presented that Roudabush incorrectly identified the organism. It is renamed as E. parasciurorum nov. sp. Mature oocysts have mean measurements of 29 × 16°, an index of 1.82, are cylindrical with rounded ends, have a dual membrane, and no extra residual body. Oocysts are without micropyle. Four egg-shaped, mature sporocysts in the oocyst have mean measurements of 11.2 × 6.2°, an index of 1.81, contain an oval, granular, intraresidual body and two pyriform sporozoites 10 × 3.2°, index 3.11.

Notes: SUMMARY. Two centrioles, an old one and a new one, are always present in the resting cell. From prophase onward two new ones and two old ones are present. Beginning with the resting stage, five types of centriole life cycles are described and compared with one another: In type 1, both centrioles are elongate; in type 2, the old one is long and the new one, which is short, elongates in prophase; in type 3, both are short, both elongate in prophase, and both, except for their anterior tips, degenerate in late telophase; in type 4, both are long but in prophase their distal ends become free of the rest of the centrioles, these ends migrate to center or posterior end of cell, where, after they produce the achromatic figure and it completes its function in nuclear division, they degenerate; in type 5, both are short and neither elongates at any stage of its life cycle.New centrioles are produced by the anterior ends of old ones. In their first generation, centrioles produce only extranuclear organelles (flagella, parabasals, axostyles, etc.); in their second and later generations, they produce only the achromatic figure (gametogenesis in Trichonympha and reorganization in Barbulanympha and Rhynchonympha are exceptions to this rule).The distal ends of centrioles in some types of cycles are surrounded by centrosomes; in others they are not. In one type of centriole life cycle a small central spindle is present in the resting cell in two genera; in the other types this is not the case.

Notes: SUMMARY. The endogenous development of the life cycle of Eimeria alabamensis Christensen, 1941, occurs in the nucleus of the intestinal cells of cattle. Calves were killed at various intervals after inoculation with infective oöcysts to study the endogenous cycle. Excysted sporozoites were found in the contents or scrapings from the walls of rumen, omasum, small intestine, cecum, and colon. They were found in the cytoplasm of intestinal epithelium at 2 days. Schizonts were found in the nuclei beginning at 2 days, but the number was low by the 8th day. Merozoite numbers usually ranged between 16 and 32. Some host nuclei contained as many as 48 or more, but these appeared to be the result of more than one schizont merging in the same host nucleus. Merozoites were slender, spindle-shaped bodies while still in the schizont walls, but were short with bluntly rounded tips when found in intracellular spaces and crypts. Gametocytes were found as early as the 4th day. Most of the stages of gametogenesis were limited to the lowest third of the small intestine, but in heavy infections some were also found in the cecum and upper colon. Microgametocytes were multinucleate and were more densely stained than the uninucleate macrogametocytes. The ratio of macrogametocytes to microgametocytes in 100 gametes was 78: 22. Oöcysis with “shells” were found in sections of the lower 20 feet of the ileum on the 6th day, which coincided with the shortest prepatent period reported previously. As many as three schizonts or microgametocytes or four or five macrogametocytes or oöcysts could be found in the same host nucleus. The variations in shape of the oöcysts appeared to be dependent on the number of oöcysts crowded into each nucleus.

Notes: SUMMARY. The role of centrioles in achromatic figure production is considered when the number present varies from 1–8. Each centriole after it becomes elongate produces astral rays from its distal end. Some of these rays remain free; some, by joining centromeres, become chromosomal fibers; and some, by joining and growing along those produced by one or more other centrioles, produce the central spindle portion of the achromatic figures. Thus, one centriole may function cooperatively with one to several others in the production of central spindles. But at least two centrioles must be present, and in the proper spacial relation to each other, to form a central spindle; one by itself can form only free astral rays, no central spindle or chromosomal fibers.The flagellated areas (to which the centrioles are anchored anteriorly) play an important role in determining the position of the distal ends of the centrioles with respect to one another, and the position of these ends, in turn, in a large measure, determines the types of achromatic figures produced, particularly the number of central spindles.

Notes: SUMMARY. Observations on binary fission of Lacrymaria olor show that it is a transverse fission. It involves probable intranuclear division of the micronucleus. Both micro- and macronucleus elongate in preliminary stages. Each is ultimately divided as cytoplasmic constriction cuts the spindle fibers of the former, and the connecting, nucleoplasmic thread of the latter.Surging movements of cytoplasm after fission elongate the daughter organisms and move new nuclei to normal, central sites. The anterior proboscis of the posterior daughter regenerates suddenly, complete with coronal cilia. Metachronal waves along ciliary meridians, strongly reversed on the posterior daughter, cause an oscillating movement which pulls the two apart, except for a slender, pellicular thread, ultimately severed. Until broken, this thread connects the rear tip of the anterior animal to the forward end of the proboscis of the posterior one. The organism is semi-quiescent, with proboscis retracted (except spasmodically) throughout fission. After fission the anterior animal quickly begins feeding movements and soon swims away. The posterior animal requires about half an hour before being able to begin feeding and swimming movements.The anterior contractile vacuole of the original animal becomes the primarily active vacuole of the anterior daughter; the posterior one that of the posterior daughter. Missing vacuoles are regenerated by the daughters in about one hour after fission. The division process requires about one hour for completion at 22.4°C.

Notes: SUMMARY. The multiplication rate of Tetrahymena pyriformis HS in proteose peptone medium was measured at 12 temperatures between 18.4°C. and 36.6°C. At the temperature optimum, 32.5°C., the generation time is 2.25 hours. The upper lethal temperature lies between 36.6°C. and 38.0°C. Similarly, a study of Tetrahymena pyriformis GL revealed a temperature optimum for multiplication of 29°C. with a generation time of 3.70 hours. The upper lethal temperature falls between 34.6°C. and 35.4°C. At all temperatures employed the HS strain of organisms multiplies more rapidly than strain GL. Under identical conditions, the two strains have distinctly different growth optima, upper lethal temperatures and growth rates.As measured by multiplication rate the readjustment to a sudden change in temperature (from 18.4°C. to 27.7°C.) is completed very rapidly, with an effective lag time of about 1 hour. Such a shift in temperature gives rise to a small degree of division synchrony during the first and second population doublings which follow. Subsequently, all traces of division synchrony are lost.

Notes: SUMMARY. Test tube cultures of Tetrahymena pyriformis GL in the early maximum stationary phase of growth were used as inocula. After the elapse of a short lag phase a rapid transition to the logarithmic phase of growth was observed in cultures grown on peptone media(4,6). During the early phase of exponential multiplication more cells (as expressed on a percentual basis of the population number) were in the visible stage of cytoplasmic fission than after the elapse of 5 to 6 generations. Analysis of comprehensive data suggests that the higher division index in the early logarithmic phase of growth is not the expression of a synchronization of cells in metabolic respects but rather indicates a prolongation of the stage of cell fission during this phase.

Notes: SUMMARY. Ochromonas malhamensis (Pringsheim strain) can be grown above 35.5°C.; below 35°, the previous chemically defined medium supports dense growth. The B12 and thiamine requirements rise steeply with temperature, and growth promotion by folic acid emerges; folic acid spares the enhanced B12 requirement. B12 is spared also, perhaps wholly bypassed, by purines + pyrimidines + amino acids (below 35°, exogenous purines, pyrimidines, and folic acid have little effect). Requirements also emerge for glycine (spared by serine), valine and isoleucine (their ratio is critical; leucine and threonine assist in maintaining a good balance), and, at very slightly higher temperatures, phenylalanine, tryptophan, cystine, and lysine. Requirements for Mg, Fe, Zn, and Mn appear to rise steeply with temperature; metal toxicities have to be circumvented carefully. The proportion of histidine + arginine to carbohydrate has to be increased, and a Krebs-cycle component such as succinic acid becomes stimulatory. At 36.3–36.7°, a further supplement of crude natural materials such as an autoclaved suspension of Ochromonas cells is needed. Relevance of these findings to fever stress in vertebrates, general mitochondrial function, and repair of radiation damage, is discussed.

Notes: SUMMARY. According to Kahl the trichostome genus Trichopelma may be considered to include five species: T. sphagnetanim, T. eurystoma, T. euglenivora, T. opaca, and T. torpens. A sixth species is added in the present account. The following constant characteristics distinguish it from the five earlier described ones: total lack of trichocysts; differences in the morphology of the body surfaces; dissimilarity of the upper and lower surfaces in shape (one plane, the other convex), in ciliation, and in number of cuticular furrows; unique location of the contractile vacuole.

Notes: SUMMARY. Isospora citelli n. sp. is described from the rock squirrel, Citellus variegatus Utah, from Grand Canyon National Park, Arizona. Its oocysts are subspherical, 22.4 by 21.5 μ, with a smooth, two-layered wall, an oocyst refractile globule and a sporocyst residuum, but without a micropyle or oocyst residuum.

Notes: SUMMARY. Leptomonads of Leishmania tarentolae were grown continuously in a defined medium containing: inorganic salts', glucose, hemin, 17 amino acids, purines and pyrimidines, and a mixture of vitamins of the B group. In this medium the population of organisms reached about 20 to 50 million per ml. alter 1 week at 27°C. Only slightly better growth occurred in a partially defined medium containing bovine plasma fraction V. In earlier experiments, however, omission of the plasma fraction resulted in decreased growth, and under these circumstances cholesterol or lecithin had growth-stimulating effects. In later experiments in the fully-defined medium no effect of these lipids could be found. The leptomonads were shown to require at least the following substances: inorganic salts; a source of purines and pyrimidines; tryptophan and the nine other amino acids essential for the growth of rats, glutamic acid, tyrosine, proline, serine, one or more of the group alanine, glycine and aspartic acid; folic acid, biotin, pantothenic acid, nicotinamide, riboflavm, thiamine, and either pyridoxine plus choline or pyridoxal or pyridoxamine. Choline at 2 × 10−5 m gave optimal growth in the presence of pyridoxine at 1 × 10−5 m. In a medium with a suboptimal concentration of choline (0.4 × 10−5 m) the leptomonads grew through nine transfers but they were mostly somewhat rounded and aflagellate.

Notes: SUMMARY. Trichopus lachmanni n. sp. possesses, in common with other members of the family Dysteriidae, a fixation organelle composed of vesicles and a secretory ampoule. But no “foot-like” appendix exists in this species, and the ampoule opens at the bottom of an antapical pit which bears a short fringe of membranelles derived from the somatic ciliature. The vibratile fringe participates in the spinning of the glutinous secretion which temporarily fastens the organism to the substrate. This specialized ciliature is characteristic of the genus Trichopus which was created by Claparède & Lachmann for a species, T. dysteria, which, though insufficiently described, is certainly different from T. lachmanni.

Notes: SUMMARY. Various species of ciliates are characterized by the formation and accumulation in the cytoplasm of mineral concretions which are refringent, isotropic or anisotropic. These cytoplasmic inclusions most often are composed of calcium carbonate; in several species, however, their nature remains partially or even totally undetermined. The isotropic calcium-containing concretions often exhibit a definite shape; the calcium carbonate in this case appears to be bound to an organic substrate. The physiological role of the calcic concretions is not known; their characteristic presence in a given species is not necessarily related to ecological conditions. In a few species the calcification is localized in definite structures: spicules, skeletal plates, or otoliths of organelles supposedly sensory in nature.

Notes: SUMMARY. The combination Tween 80 and cholesterol replaced blood serum as a requirement for the cultivation of Tritrichomonas foetus. Choline + potassium glycerophosphate enhanced growth in the presence of Tween 80 + cholesterol. A method for ensuring adequate cholesterol suspension-an essential factor for consistent growth-is described.

Notes: SUMMARY. High variability within cultures of Tritrichomonas batrachorum (from Bufo boreas halophilus, Rana catesbeiana, and Rana pipiens) casts doubt on the validity of length measurements for species designation.The morphology differs from that described previously. The axostylar capitulum is a complex structure with a preblepharoplastic portion and a perinuclear cup spreading laterally in curved membranes ending in filaments. The parabasal apparatus is Y-shaped with a very short base.Two types of amoeboid activity occur. Filopodia are used for anchorage. Their bases migrate and the filopodia may fuse and reseparate as in foraminifers. Ingestion is an amoeboid process utilizing lobopodia. Food adherent to a lobopod is invested in a food cup at the surface. Ingrowth of the lip of the food cup forms the food vacuole, or in cases of cannibalism, constricts the prey and forms a food tube pushing a vacuole before it. Repeated, this produces an alternating series of vacuoles and tubes. There is a pseudo-amoeboid degenerative process in which the flagella, withdrawn into the cytosome, continue to move and produce non-functional lobopod-like protrusions.An actual cytostome has not been observed, but there is a region of reduced staining intensity ventral to the axostylar capitulum.

Notes: SYNOPSIS. Thymidylate synthetase (E.C.2.1.1.45) has been demonstrated in unsporulated oocysts of Eimeria tenella. The properties of this enzyme have also been investigated in Tetrahymena pyriformis, as a protozoan model, and 7-day-old chick embryo, as a host model. The enzymes from E. tenella and chick embryo were inhibited by all concentrations of MnCl2 and MgCl2 tested. Tetrahymena pyriformis thymidylate synthetase was stimulated by low concentrations of both these cations but was inhibited by high concentrations. Subsequent data refer to chick embryo, E. tenella and T. pyriformis respectively: the apparent Km was 5.89 μM, 5.94 μM, and 0.53 M for the substrate dUMP: and 5.13 μM, 1.10 μM and 4.65 μM, respectively for the cofactor N5N10-methylenetetrahydrofolate. The pH optimum for the enzyme from both chick embryo and T. pyriformis was 8.0, with Tris-HCl buffer; activity of E. tenella thymidylate synthetase was still increasing at pH 8.2. The E. tenella enzyme was found to have a molecular weight of 4.6–4.9 × 105 daltons. The effects of nucleotides, inhibitors, and the omission of assay components on each enzyme are presented. Thymidylate synthetase from E. tenella is not greatly different from that of chick embryo, but does not resemble the enzyme from T. pyriformis. A case for using thymidylate synthetase as a chemotherapeutic target in the treatment of Eimeria infections remains. Indeed Eimeria may be considered as a model for infections caused by other protozoan parasites, such as Toxoplasma and Plasmodium, provided that suitable inhibitors can be found that are not toxic to the host.

Notes: SYNOPSIS. A protocol based on density differences between starved and fed cells and employing density gradient centrifugation has been devised to facilitate the isolation of auxotrophic mutants of cell lines derived from Tetrahymena thermophila strain B1868. First, a mass phenotype screening procedure was established whereby true auxotrophic mutants and slow-growing wild-type cells such as strain C* could readily be distinguished. Second, simulation experiments were performed in which wild-type cells starved first in non-nutritive buffer, then suspended in a defined medium lacking a single essential amino acid became significantly denser than the same cells when starved, then suspended in a complete defined medium. Finally, using the same protocol, a reconstruction experiment was carried out which resulted in effective separation of wild-type cells from cells of a tyrosine auxotroph. The overall procedure resulted in a 9-fold increase in the relative frequency of auxotrophic cells, while the density gradient centrifugation alone provided a 400-fold enrichment.

Notes: SYNOPSIS. Infectivity of Plasmodium gallinaceum (Brumpt) sporozoites isolated from midguts and salivary glands of experimentally infected Aedes fluviatilis (Lutz) was studied. The 2 populations were compared at 7, 8, and 9 days postisolation from mosquitoes, which were maintained at 27 C ± 1C and ∼75% relative humidity. Infectivity of the parasites was evaluated by the length of the prepatent period of the infection in 2-week-old chicks inoculated intramuscularly. Infection was caused by 7-day-old sporozoites from salivary glands, but not from midguts. Older sporozoites induced infection in all the inoculated chicks. The results suggested a somewhat higher infectivity of the 8- and 9-day salivary-gland parasites than of the oocyst sporozoites. However, unlike sporozoites from mammalian malaria, oocyst sporozoites from avian malaria were highly infective at this age.

Notes: SYNOPSIS. Sorogena stoianovitchae Bradbury & Olive, an epiphytic ciliate found in various parts of the world, has a trophic stage that feeds on members of the ciliate genus Colpoda. When grown in the presence of the food ciliate, it multiplies rapidly. When the cells become abundant they aggregate at the water surface on inserted plant fragments or floating pollen grains, the sides of culture dishes, or on floating films such as those deposited by bacteria or pollen grains. an aggregate mounds up and becomes ensheathed above the water level, after which the mass of cells called a sorogen rises aerially at the apex of a stalk deposited at its base. the tapering, noncellular stalk consists of a conspicuously furrowed sheath that encloses a mucilaginous matrix. At completion of stalk development the cells of the sorogen become encysted. the sorocysts are commonly discharged by fracturing of the drying sorus. Alternating light and dark conditions are required for sorocarp development.

Notes: SYNOPSIS. the antigenic types in populations of metacyclic trypanosomes of Trypanosoma brucei isolated from Glossina morsitans head-salivary gland trypanosome cultures and bloodstream forms in the early parasitemias produced from whole culture supernatant fluids containing metacyclic forms, were analyzed by the indirect fluorescent antibody test using clone-specific antisera. Metacyclic trypanosomes in cultures initiated with cloned bloodstream forms were heterogeneous with respect to their variable antigenic type (VAT). Trypanosomes comprising early parasitemias in immunosuppressed mice infected with metacyclics produced in cultures also had a range of VATs. Three of the VATs detected in the early parasitemias in mice have also been identified by other investigators in tsetse fly-transmitted populations of the same stock.

Notes: SYNOPSIS. A simple method is described for plating and cloning ciliates and other protozoa, based on a principle differing from that traditionally used for plating and cloning bacteria and other microorganisms. This procedure, referred to as the silicone-oil-plating-procedure (SOPP), involves vortexing small volumes of culture medium containing protozoa with larger volumes of a non-toxic silicone oil and plating the resulting unstable emulsion in small plastic petri plates. Discrete microdroplets of culture medium form containing protozoa entrapped and immobilized between the hydrophobic surfaces of the plastic petri dish and the oil. Protozoa, isolated by this method grow, divide, and multiply to form clones. the procedure may be used for plating and cloning protozoa in bacterized and axenic culture. Variations of the basic method may be applied to isolating protozoa from the wild, washing protozoa to remove microorganisms, screening for potential mutants, and for replica plating.

Notes: SYNOPSIS. Cyclic nucleotide phosphodiesterase [EC 3.1.4.17] was examined in Tetrahymena pyriformis strain NT-1. Enzymic activity was associated with the soluble and the particulate fractions, whereas most of the cyclic GMP phosphodiesterase activity was localized in the soluble fraction: the activities were optimal at pH 8.0–9.0. Although very low activities were detected in the absence of divalent cations, they were significantly increased by the addition of either Mg2+ or Mn2-. A kinetic analysis of the properties of the enzymes yielded 2 apparent KIII values ranging in concentration from 0.5 to 50 μM and from 0.1 to 62 μ M for cyclic AMP and GMP. respectively. A Ca2+-dependent activating factor for cyclic nucleotide phosphodiesterase was extracted from Tetrahymena cells, but this factor did not stimulate guanylate cyclase [EC 4.6.1.2] activity in this organism. On the other hand, Tetrahymena also contained a protein activator which stimulated guanylate cyclase in the presence of Ca2+, although this activator did not stimulate the phosphodiesterase. the results suggested that Tetrahymena might contain 2 types of Ca2+-dependent activators, one specific for phosphodiesterase and the other for guanylate cyclase.

Notes: SYNOPSIS. the cell size of Didinium nasutum was found to be dependent on the size of the Paramecium species available as prey. Didinium feeding on P. tetraurelia averaged 5.6 × 105μm3. the cell volume of Didinium increased with increasing prey size for the 5 prey species tested, to 9.1 × 105μm3 for Didinium feeding on P. caudatum. Didinium nearing a cell division ranged in size from 8.6 × 105μm3 on P. tetraurelia to 12.9 × 105μm3 on P. caudatum. the range in cell volume is such that Didinium feeding on P. caudatum are larger than the size at which Didinium divide when feeding on P. tetraurelia. This morphologic plasticity in cell volume allows Didinium to exploit a wide size range of Paramecium species as prey. It is proposed that the size of a Didinium may have profound effects on its ability to encounter and capture prey of different sizes.

Notes: RESUME. Chacun des 45–80 organelles adoraux de Bursaria truncatella O. F. Müller est constitué de 3 rangées de cinétosomes et l'aire buccale droite est couverte de nombreuses doubles rangées de cinétosomes. La stomatogenèse débute par la désorganisation et la résorption des organelles buccaux postérieurs. Puis, il y a désorganisation des rangées parorales de cinétosomes et multiplication des cinétosomes sur l'aire orale droite, en měme temps que sont rompues, selon une ligne oblique, un certain nombre de cinéties somatiques. La prolifération des cinétosomes aux extrémités des cinéties. de part et d'autre de la ligne de rupture, aboutit, d'une part, à la formation d'un champ anarchique qui est le primordium oral droit de l'opisthe, d'autre part, à la formation de nombreux doublets qui constituent chacun le primordium de chaque organelle adoral. Après la séparation des tomites, les cinétosomes de l'aire droite s'ordonnent en doubles rangées et les organelles adoraux se complètent par addition d'une 3ème rangée de cinétosomes. Les cinétosomes somatiques sont jumelés, reliés par 2 desmoses. Les fibres transverses postérieures et les fibres postciliaires forment de longs rubans de microtubules dirigés vers l'arrière et juxtaposés dans les crětes intercinétiennes. Les doubles rangées droites de cinétosomes buccaux sont assimilables à des stichodyades. Les organelles des cinétosomes adoraux portent des rideaux de fibres postciliaires convergents ou divergents. La rangée postérieure de chaque organelle est non ciliée. Par son type de stomatogenèse, par sa structure corticale, par l'ultrastructure des organelles adoraux, Bursaria appartient aux Colpodidea, ce qui suggère des remarques de plusieurs types.SYNOPSIS. In Bursaria truncatella O. F. Müller, each of the 45–80 adoral organelles is composed of 3 rows of kinetosomes, and the right buccal area is covered by many double rows of kinetosomes. Stomatogenesis begins by disorganization and disappearance of the posterior buccal organelles. Next, there is disorganization of the paroral rows of kinetosomes and multiplication of kinetosomes in the right oral area; at the same time, some somatic kineties are disrupted along an oblique line. Multiplication of kinetosomes at the extremities of the kineties, on both sides of the disruption, leads to the formation of an anarchic field which is the right oral primordium of the opisthe and the formation of doublets each of which constitutes an adoral organelle. After the separation of the tomites. the kinetosomes in the right buccal area position themselves, and the adoral organelles are completed by the addition of a 3rd row of kinetosomes. Somatic kineties are formed by successive pairs of ciliated kinetosomes united by 2 desmoses. the long posterior transverse ribbons and the postciliary ribbons extend posteriad, overlapping in the pellicular ridges. Oral rows of kinetosomes on the right can be compared with stichodyads. the adoral kinetosomes have convergent or divergent postciliary ribbons. the posterior row of kinetosomes in each organelle is not ciliated. By the type of stomatogenesis, the cortical ultrastructure, the ultrastructure adoral of its organelles, Bursaria belongs to the Colpodidea.

Notes: SYNOPSIS Free-living marine ciliates occur in the interstitial spaces of a wide vareity of filamentous and particulate substrata, on the surfaces of planar substrata, and in the plankton. In addition, they are found in association with a wide variety of plant and animal hosts. In this paper I review the progress during the past decade in understanding the distribution of marine ciliates, with particular emphasis on the relationship between ciliate biogeography and the species problem. It is concluded that as a general rule among marine ciliates, genera and species complexes are cosmopolitan. Specific locales may support a confusing array of sibling species or subspecific morphologic variants. Because the distributional processes and breeding biology of marine ciliates are only beginning to be understood, conventional ideas that marine ciliate species are cosmopolitan may require modification.

Notes: SYNOPSIS The subkingdom Protozoa now includes over 65,000 named species, of which over half are fossil and ∼ 10,000 are parasitic. Among living species, this includes ∼ 250 parasitic and 11,300 free-living sarcodines (of which ∼ 4,600 are foraminiferids); 1.800 parasitic and 5,100 free-living flagellates: ∼ 5,600 parasitic “Sporozoa” (including Apicomplexa, Microspora, Myxospora, and Aseetospora); and ∼ 2,500 parasitic and 4,700 free-living ciliates. There are undoubtedly thousands more still unmamed. Seven phyla of PROTOZOA are accepted in this classification—SARCOMASTIGOPHORA. LABYRINTHOMORPHA, APICOMPLEXA, MICROSPORA, ASCETOSPORA, MYXOSPORA, and CILIOPHORA. Diagnoses are given for these and for all higher taxa through suborders, and representative genera of each are named. the present scheme is a considerable revision of the Society's 1964 classification, which was prepared at a time when perhaps 48,000 species had been named. It has been necessitated by the acquisition of a great deal of new taxonomic information, much of it through electron microscopy. It is hoped that the present classification incorporates most of the major changes that will be made for some time. and that it will be used for many years by both protozoologists and non-protozoologists.

Notes: SYNOPSIS Leishmania donovani amastigote-to-promastigote transformation is inhibited by homogenates of infected hamster liver and spleen. This inhibitory activity is localized in the 100,000 g pellet fraction. Tests with lysates of adherent (macrophyages) and nonadherent (lymphocytes) spleen cells indicated that the inhibitory activity resided in the lymphocytes, specifically in the 100,000 g pellet fraction.

Notes: SYNOPSIS Antibodies induced in rabbits against Paramecium multimicronucleatum syngen 2 prevent sexually reactive cells from clumping, pairing, and forming cytoplasmic fusions. A biologic assay for the detection of these antibodies (designated blocking antibodies) is described. the blocking antibodies, unlike the immobilization antibodies, are produced against breis of sexually reactive cells and nonreactive cells of 2 types, nonstarved and immature. Isolated cilia from reactive cells of either mating type are weak immunogens for blocking antibodies. No correlation between the mating type specificity (III or IV) and these antibodies has been detected. Blocking antibodies can be absorbed with living cells, of which sexually reactive ones are the most effective absorbers, while immature ones are the least effective.

Notes: SYNOPSIS A method is described for the axenic mass cultivation of Paramecium tetraurelia strains 51s and 299s. the ciliate is grown in an enriched axenic medium developed by Soldo, Godoy & van Wagtendonk. Under continuous shaking on a rotary shaker, cultures were grown in one-liter Erlenmeyer flasks with 330 ml medium yield cell densities of 32,000 cell/ml and 20,000 cells/ml for strains 299s and 51s respectively. Doubling time is considerably shorter under these conditions than in the conventional static cultures. A 20-liter airlift bioreactor is described in detail which can be used successfully to otain up to 100 g wet weight of Paramecium in a single run; in this reactor the cell density reaches 38,000 cells/ml for strain 299s. and 23,000 cells/ml for 51s. This technic should facilitate the study of minor protein components of the ciliate.

Notes: SYNOPSIS The cadmium ion (Cd2+) was accumulated by Amoeba proteus in all cellular fractions, the highest level being associated with the cytosol fraction. On gel separation of the cytosol fraction, Cd-binding protein appeared in 2 peaks: one 〉45,000 MW (peak I) and the other 12,000 MW (peak II). Added cysteine increased the total Cd2+ taken up by the cells and resulted in disproportionate increase of Cd incorporated into the Cd-binding protein of peak II. the Cd-binding protein of peak II is analogous to the low-MW, Cdbinding proteins in Anacystis nidulans, Mytilus edulis, and to the metalloprotein of some vertebrates.

Notes: SYNOPSIS. The oocysts, sporulation process, and endogenous stages of Eimeria raillieti (Léger, 1899) Galli-Valerio, 1930 from the slow-worm, Anguis fragilis, in England are described. The oocysts average 18 × 15 μ. Schizonts, microgametocytes and macrogametocytes were found in the ileum, and macro-gametocytes alone in the duodenum.

Notes: SYNOPSIS. Zooxanthellae in pure culture, exposed to continuous light, release free O2 in amounts varying with time and cell number. Zooxanthellae exposed to alternate light and dark produce essentially as much O2 as in continuous light. Those in continuous dark do not yield free O2; rather, they draw from the medium's residual O2.Both the anemone Condylactis and the scyphozoan Cassiopeia are markedly phototactic. Kept in total darkness, both species show a dramatic numerical diminution in zooxanthellae. During 24 days of darkness, the mean total number of zooxanthellae in the individual Condylactis body was reduced from 26 million to ∼ 1 million. Specimens so bleached lost phototaxis.It is suggested that each species of zooxanthella host animal has its own specific light needs, which it caters to in various ways: (a) early selection of position, as with planulae or other freely motile larval forms; (b) gross body movement or posturing, as with anemones, medusae, and worms; (c) possession of light-filtering pigments, as with colored corals and molluscs; (d) possession of light-concentrating devices, as with tridacnids; (e) possession of highly contractile and differentially light-absorbing tissues, as with most coelenterates and some molluscs.Susceptibility of marine invertebrates to zooxanthellae infection may be related to the known paucity of nitrates and phosphates in tropical seas, a situation possibly inducing the free-swimming gymnodinioid forms to enter animal tissues where catabolic products are available to them. Zooxanthellae are reported from sessile marine invertebrates taken at depths of 100–116 fathoms.

Notes: SYNOPSIS. All of 99 adult English house-sparrows, examined in the St. Albans area of Hertfordshire, England, were found to be infected with the organism previously defined by Garnham (1950) as Atoxoplasma. Young birds were found to become infected while still in the nests and as early as 6 days after hatching; there was no evidence to suggest that the parasite was transmitted through the egg. Within a few weeks of leaving the nests, all of 150 fledgling sparrows examined were heavily infected and several trapped birds died from massive infections.All stages of schizogony were found in the lymphoid-macrophage cells of the spleen, bone marrow and liver of these birds; later, as the schizogonic cycle abated, gametocytes developed in similar cells of the liver, lungs and kidney. These gametocytes are of the Eimeria type: the zygote nucleus divides to produce an asporous and polyzoic oocyst containing a large number of sporozoites, and after the rupture of the oocyst these sporozoites invade the lymphocytes and monocytes of the peripheral blood.Transmission of the parasite in the sparrow is thought to take place after the ingestion of infected mites (Dermanyssus gallinae) by the young birds in the nests: unchanged sporozoites were found in smears of these mites that had been fed on infected sparrows. Transmission experiments were impossible due to the complete lack of clean sparrows.The taxonomic status of Atoxoplasma is discussed. The type of life cycle and the production of asporous, polyzoic oocysts indicate inclusion of this parasite in the Order Coccidiida, Family Eimeriidae, Sub-Family Cryptosporidiinae Hoare, 1933. After comparison of the two genera, the author concludes that Atoxoplasma must be regarded as a synonym for Lankesterella. Some previously described species of Atoxoplasma are, therefore, transferred to the genus Lankesterella.The name Lankesterella garnhami nov. sp., is proposed for the parasite in the English sparrow (Passer domesticus domesticus), and Lankesterella serini nov. sp., for that in the canary (Serinus canarius).

Notes: SYNOPSIS. Darkness and O2-lack promote formation of a pheophytin-like pigment from chlorophyll in Euglena gracilis in an acidic medium. Dinitrophenol (DNP) produces similar but more drastic pigment alterations in aerated and illuminated cells. The extent of pigment decay was dependent on DNP concentration and external pH. Since volume expansion and inhibition of the contractile vacuole were also noted, it is suggested that pheophytin formation is secondary to hydrogen ion influx from the external medium. Major structural alterations of the chloroplast accompanied the pigment changes.Pentachlorophenol, iodoacetamide, Na fluoride, and Na azide produced similar pigment changes. Malonic acid and fluoroacetate were ineffective under the conditions described. However, in the dark, cells treated with fluoroacetate formed pheophytin rapidly. These effects are discussed in relation to the maintenance of intracellular [H+].

Notes: SYNOPSIS. The heterotrophic, phototrophic, and phagotrophic nutrition of the chrysomonad flagellates Ochromonas malhamensis and O. danica were compared. Unlike O. malhamensis, O. danica, which is much richer in chloroplast pigments, grew readily photoautotrophically in a substrate-free medium in 5% CO2. Utilization of bound biotin in bacterial (Thiobacillus) bodies served to demonstrate phagotrophy in both flagellates. This nutritional versatility suggests that this group of flagellates will be exceptionally valuable for studying the evolutionary steps connecting photoautotrophy, heterotrophy, and phagotrophy.

Notes: SYNOPSIS. In a synthetic medium containing 57 compounds, including cholesterol, Trichomonas gallinae and T. gallinarum require 3 factors for growth and acid fermentation of maltose: (1) factor R, found in the protein contaminating some samples of ribonucleic acid, and in other isolated proteins such as conalbumin, γ-globulin, and bovine albumin fraction V; (2) factor T, found in Trypticase and in the same isolated proteins, but with activity at 4 times the dose required for factor-R activity, may be a large peptide containing proline; (3) factor S, found in serum, was replaceable by a saturated and an unsaturated fatty acid, each inactive alone. Only C14 through C18 saturated fatty acids were active over a range of 0.058 to 2.34 μm per tube in the presence of oleic acid, while C18 through C22 unsaturated fatty acids were active in the same range with palmitic acid as the supplement. The unsaturated fatty acids were toxic at the largest dose. All fatty acids were not equally active. Surface-active agents containing mixtures of fatty acids also replaced serum. A 4th factor, found in serum, stimulates the rate of growth as shown by cell counts at 3 days of incubation. T. gallinarum, T. foetus, and a trichomonad from a pig's nose responded to the same supplements when grown on another synthetic medium.

Notes: SYNOPSIS. Differences in temperature-tolerance, generation time, nutritional requirements, osmoresistance, pigment production, and sensitivity to high hydrogen or hydroxyl ion concentration have been observed among varieties, and among mating types within varieties of Tetrahymena pyriformis. The usefulness of these differences to taxonomists and geneticists is discussed.The nutrition of a temperature-tolerant strain, mating type II, variety 1, was given special attention and a chemicallydefined medium devised to support rapid growth at 35d̀ C. At 40d̀, growth in this medium failed, but was good in a crude medium. Temperature factors are suggested. Permeability of this ciliate, as inferred by utilization of nucleotides, was high.

Notes: SYNOPSIS. Eight strains of Tetrahymena pyriformis were examined in multiple daily isolation series over ∼ 800 generations. Dead and defective lineages appeared in all clones. In 7, the defective sub-lines appeared at a constant characteristic rate; the 8th showed an increasing rate of production of two defects. A breeding analysis of certain persistent morphological and growth rate variants suggests that the variations derive from macronuclear alterations. The relationship between these cellular changes and “senility” in metazoa and other protozoa is discussed.

Notes: SYNOPSIS. An acetone-insoluble yeast fraction required for axenic growth of P. aurelia, stock 51, variety 4, sensitive, after fractionation contained at least 3 essential components: (1) one soluble in perchloric acid and completely replaceable by a mixture of ribosides or ribotides; (2) one inactivated after digestion with trypsin, chymotrypsin or papain. Proteose-Peptone restored activity to this preparation, which suggests a peptide requirement; and (3) one not yet characterized.As for the purine and pyrimidines, these combinations, in decreasing order of activity, supported growth: guanosine + cytidine, guanosine + uridine, guanylic acid + cytidylic acid, and guanylic acid + uridylic acid. Each combination was maximally effective when the molar purine: pyrimidine ratio was ∼ 0.4. On a molar basis, the minimal riboside combinations were ∼ 1.3 × more active than the ribotides.Sparing of the purine and pyrimidine requirement was also investigated. In the presence of limiting amounts of guanylic acid, the following compounds, in decreasing order of activity, had sparing activity: deoxyguanosine, inosine, xanthosine, adenylic acid, and guanine. Adenine, adenosine, and deoxyadenosine were inhibitory under the test conditions. The requirement for cytidylic acid was spared by deoxycytidine, uridine, uridylic acid, deoxyuridine, thymidine, thymine, and uracil, in descending order.

Notes: SYNOPSIS. In reviewing 25 years of work on Tetrahymena, the author describes early difficulties experienced by himself and others in developing a chemically-defined medium and in defining the taxonomy of T. pyriformis. With identification of its essential requirements, a variety of nutritional studies revealed the close resemblance between the metabolic pathways of this ciliate and those of the chick and rat. This suggested studies on the effects of gamma radiation and the effect of antibiotics.Attention then turned to the puzzle of the absence of conjugation in all strains of T. pyriformis then maintained in laboratories. The observation that these strains were all amicronucleate led to the discovery of mating types (with D. F. Gruchy). This brought up the problem of what constitutes a species and how it might be solved in T. pyriformis where clearly defined groups are set off from other similar groups (varieties) by a breeding barrier.Another problem is whether a life cycle exists in this ciliate and if so, the role amicronucleate strains play in this cycle.The origin and obvious evolutionary success of these “genetically dead” strains are other problems that are considered.The search for nutritional markers for genetic experiments inspired large-scale collections, including some from tropical habitats. Strains were found which differed in serine and pyridoxine requirements. Genetic analysis was hindered by the high lethality following conjugation, unsatisfactory mating behavior in some clones, and the complete absence of autogamy, the latter making it difficult to obtain homozygous clones. The use of x-radiation yielded haploid individuals; when these were mated with diploid clones the resulting haploid progeny proved that the genes controlling mating type and pyridoxine synthesis resided in the micronucleus.Genetic analysis of the serine and pyridoxine mutants supports the idea that T. pyriformis is more of an outbreeder than an inbreeder. Left for the future is an extension of our knowledge of the breeding system of T. pyriformis and ultimately to examine critically the factors responsible for the success of this ubiquitous ciliate.

Notes: SYNOPSIS. During encystment of Colpoda cucullus (O. F. Müller) the respiratory rate decreases from about 11.3 × 10-5μl. O2/hr. (mean value for active form) to about 1.3 × 10-5μl./hr. (mean for unstable cyst); the process takes about 24 hrs. At the same time the activity of the contractile vacuole is stopped, but there is no correlation in time between the two processes: when respiration is inhibited by 1/2–2/3 the vacuolar activity is hardly changed. The respiration of unstable cysts remains approximately constant at least for 4 weeks. Experiments with methylene blue suggest that inhibition of respiration at encystment may be due to inhibition of terminal oxidase.

Notes: SYNOPSIS. Two isolates (“A” and “B”) of Trypanosoma lewisi from the same rat stock source were serially transferred in calorically-restricted mice supplemented daily with normal rat serum. The “A” strain was transferred consecutively through 300 mice over a period of more than 3 years and was voluntarily discontinued. The “B” strain died out spontaneously after 43 consecutive passages in mice. The developmental histories of these 2 isolates were analyzed and compared with respect to duration of the parasitemic period, interval to the next subsequent passage in mice, day of death of each host animal, proportion of host animals that died, intensity of parasitemia in mouse tail blood, interval required for development of the observed maximal parasitemia, and duration of maximal parasitemia.“A” appeared to have become progressively adapted to the mouse as judged by a decrease in parasitemic period with successive transfer associated with a progressive increase in trypanosome population, and declines in the interval required for development of the observed maximal parasitemia and in the duration of this maximal response. There did not appear to be any correlation of the percentage of animals that died with any other factor. The “B” strain did not appear to have adapted itself to mice as judged by the foregoing criteria.

Notes: SYNOPSIS. The Indian race of Blepharisma undulans described in this paper measures 150 μ in length. The macronucleus consists of 5–7 nodes, all of equal size. During binary fission, condensation of macronucleus is followed by its elongation and a thinning of the middle region which breaks with the division of the animal. It later attains the typical vegetative form.During conjugation 7 or 8 micronuclei pass through the first pregamic division, 5 to 7 through the second pregamic division and one product of the second division takes part in the third division. The rest degenerate. At the same time, the macronucleus also starts degenerating. After the synkaryon has divided twice, the conjugating pairs separate. Of the 4 products, 3 become macronuclear anlagen and one, micronuclear anlage.The micronuclei divide asynchronously both during binary fission and during conjugation. There is apparently considerable diversity in the structure and behaviour of the macronucleus and micronuclei in the different races of Blepharisma undulans.

Notes: SYNOPSIS. In cattle fed a high-starch diet, species of Entodinium and Diplodinium ingested associated ruminal bacteria. Stained preparations of diluted rumen contents showed Entodinium caudatum, E. minimum, E. dubardi, (syn. E. simplex), E. longinucleatum, E. bursa, E. nanellum, E. exiguum, and E. vorax contained gram-positive diplococci. Starch grains with adherent gram-positive diplococci were observed within Entodinium spp. Diplodinium ecaudatum forma ecaudatum, D. ecaudatum forma caudatum, D. neglectum and an unidentified species of Diplodinium also ingested ruminal diplococci. Bacteria were isolated from mixed species of Entodinium by washing and culturing the protozoa in a starch feed-extract agar medium. The strains isolated from the ciliates were gram-positive diplococci, 0.8 times 1–1.5 μm, which attached themselves to starch granules and were able to digest the starch. Conclusive evidence of bacterial ingestion by the oligotrichs was obtained by providing the bacterial cultures to Entodinium species (E. dubardi and E. minimum) which had been starved 24 hr. Gram-stained preparations showed the ciliates readily ingested the bacteria. The amylolytic cocci utilized by Entodinium spp. were identified as Streptococcus bovis.

Notes: SYNOPSIS. Lankesterella corvi n. sp. (Coccidia, Eimeriidae, Cryptosporidiinae) is described from the rook, Corvus f. frugilegus L. in England. It was found in 36 of 196 fledged rooks less than 1-year old, but not in 25 nestlings or 38 adults. It was not found in 71 jackdaws (C. monedula spermologus) or in 110 other birds of 16 species.Mature sporozoites were found in the erythrocytes and occasionally in other blood cells. They were 6.2 times 2.5 μ, with a central, band-like nucleus, and cytoplasm which failed to stain with Giemsa's stain. Gametogonic and sporogonic stages, found in the bone-marrow of one bird, resembled corresponding stages of Eimeria.A fledgling rook was infected experimentally by inoculation of a blood and tissue suspension from an infected bird. Sporozoites appeared in its blood 4 days after inoculation. They appeared to increase slightly in size and their cytoplasm lost its initial affinity for Giemsa's stain during the next few days. Engorged mites (Ornithonyssus sylviarum) from the experimentally infected rock contained unchanged sporozoites but no developmental stages of the parasite. A canary could not be infected by intraperitoneal inoculation and feeding of such mites.

Notes: SYNOPSIS. A dichotomous, analytical key is offered for use in recognition and differentiation of the 26 orders and suborders belonging to the two subclasses of the single class Ciliata of the subphylum CILIOPHORA. The basic terminology employed in these brief characterizations, usable in systematic studies of ciliates in general, is defined first, and a plea is made for a more uniform vocabulary, especially in reference to structures which are without doubt homologous throughout the several higher ciliate taxa. Particular emphasis is placed on the all-important features in the oral area; many of these are figured as well as being described in words.Both the key and the definitions are essentially the first to be offered since Kahl's monographic work on the ciliates published in 1930–1935. They are demanded by the great accumulation of new pertinent data in the protozoclogical literature of the past 25 years.

Notes: SYNOPSIS. The flagellate, Peranema trichophorum, has been studied in the electron microscope by thin-sectioning techniques. The flagella have the fibrillar pattern typical of cilia and flagella, but accessory structures including tapered, intraflagellar rods, striated, layered material on the outside of the membrane, and mastigonemes are present. In the near basal region of the flagellum, there is a swelling of the shaft which is correlated with the absence of the two central flagellar fibrils. The basal portion of the intraflagellar material is structurally and locationally similar to the basal parts of the flagellar fibril bundle; this similarity suggests that the two structures originated from similar precursors and that two kinetosomes comprise the light microscopist's blepharoplast in this organism.The ridged pellicle is composed of 3 membranes, only two of which follow the contour of the ridges. Several filaments 21 mμ in diameter are localized under the low point of each ridge, and a single, larger fibril which has a periodic structure is often located beneath the high point of each ridge.The cytostome and structures associated with it are described and discussed in relation to food taking. The pharyngeal rods are cross-connected and each is composed of numerous tubular elements surrounded by a denser, homogeneous layer. A system of membranes is attached to the rods and extends anteriorly.The nucleus contains two large nucleoli, numerous rod-shaped, membrane-limited bodies which appear similar in structure to bacteria, and a smaller granular component.Other organelles are briefly described including mitochondria, Golgi bodies, vacuoles, and endoplasmic reticulum.

Notes: SYNOPSIS. Materials within the endoplasm of both the protomerite and deutomerite may be displaced and stratified by ultracentrifugation. Animals are not killed by this treatment, and in time a redistribution of stratified materials may occur. The electron microscope reveals numerous ultramicroscopic folds in the surface envelope which is composed of 3 membranes; the outer and middle cover the surface of the folds while the inner one continues as a smooth membrane over the ectoplasm. The contact surfaces of animals in syzygy do not show the small folds to be interlocked; instead, they are in fold-to-fold contact. Numerous relatively dense bodies which appear to be filamentous are sometimes observed immediately underneath or within the middle or inner membrane. Within the ectoplasm is an ultramicroscopic net-like fibrillar structure much denser than the surrounding cytoplasm. This system of fibrils is composed of anastomosing elements varying from ∼ 50 to 200 Å in diameter. Certain of the larger fibrils are directly attached to the surface envelope at positions between the folds. A second filamentous structure within the ectoplasm appears to be tubular. Elements of this system also appear to join and penetrate the surface envelope by means of pores.A large amount of gelatinous secretion forms at the surface of the sporont; as it glides forward a trail of mucous is left behind. The actual mechanism involved in the gliding movement was unobserved, but evidence is lacking to support the view that the gliding movement is engendered by posteriorly directed “jets” of mucus.

Notes: SYNOPSIS. Vorticellas were subjected to achromycin, polymyxin, and mixtures of penicillin-streptomycin to remove bacterial contaminants. Although achromycin and polymyxin were most effective in controlling bacteria isolated from vorticella cultures, they proved too toxic for practical use. However, certain dilutions of penicillin-streptomycin were tolerated by vorticellas and, therefore, were incorporated into the axenizing procedure. Yeasts did not yield to the antibiotics and had to be removed by washing and dilution. Sterile vorticellas were finally obtained by transfer of groups of individuals through 6 washes. One of these, the 4th, lasted 8 hours and contained diluted penicillin-streptomycin.

Notes: SYNOPSIS. The interphase nucleus of Lesquereusia spiralis, a testate rhizopod, 20–25 μ in diameter, contains 40–50 endosomes and a diffuse granular reticulum. Onset of nuclear division is marked by a cessation of pseudopod activity. Prophase changes include increase in size of the nucleus, disappearance of the endosomes except the peripheral ones, formation of 175–200 chromosomes from the reticulum, and the appearance of spindle fibers. By the end of prophase a well formed equatorial plate is present. The metaphase nucleus is slightly smaller and elongated; the chromosomes remain distinct. In anaphase the nucleus continues to elongate along the polar axis; the chromosomes apparently split lengthwise and polar caps appear. The nucleus elongates further so that by telophase it has become hour-glass shaped. The spindle fibers are now twisted. Separation of the nuclei takes place in the neck region. The nuclear membrane is unbroken during the process and peripheral endosomes are present at all stages. Total time for mitosis averages 45 minutes.

Notes: SYNOPSIS. Three gregarines are described from the digestive tracts of marine crustacea from Bombay, India. These are Carcinoecetes etisi n.sp. from Etisus laevimanus, C. matutae n.sp. from Matuta lunaris, and Caridohabitans setnai n.gen., n.sp. from Peneus semisulcatus. Various life history stages are reported.

Notes: SYNOPSIS. In various ciliates the contractile vacuole is a permanent organelle, delimited by a differentiated cortex.The cortex is made up of a dense reticulum of anastomosing tubules limited by a smooth membrane, and vesicles. This “spongiome” can be considered as a localized and specialized condensation of the endoplasmic reticulum.

Notes: SYNOPSIS. Two species of flagellate parasites, Herpetomonas muscarum (Leidy 1856) Kent 1881 and Crithidia luciliae (Strickland 1911) have been isolated in pure culture from the fly, Phaenicia sericata. Laboratory-reared Musca domestica were infected with each of the species. These two species have often been confused, the latter being regarded as “cysts” of the former. H. muscarum is long and slender and occurs actively swimming in the midgut of the host. C. luciliae is short and truncate and occurs mainly in the hindgut where it is often attached to the gut wall. C. luciliae grows readily and abundantly in culture and outgrows H. muscarum in mixed cultures. Attempts to infect Aedes aegypti and Culex pipiens with C. luciliae failed while control feedings of these mosquitoes with Crithidia fasciculata produced infections.

Notes: SYNOPSIS. Trimastigamoeba philippinensis Whitmore 1911 from Florida was cultured in the laboratory at 22 to 25° C. on a modified Bunting's agar medium overlaid or not with Neff's ameba-saline. Studies of its general morphology, transition from ameboid to flagellate phase and vice versa, encystment, and excystment were made. In general, Whitmore's observations are confirmed, except for his conclusions concerning the number of flagella and whether or not there is a rhizoplast. The flagellate phase has two mastigonts, each composed of a pair of flagella attached to a basal granule (blepharoplast). Intermediate stages in the development of the mastigonts may have caused Whitmore to decide that a tri-flagellar phase was the usual condition. The two mastigonts are not at any time attached to one another, nor to the nucleus, nor is there any evidence of a rhizoplast or rhizostyle. In the flagellate phase the bases of the mastigonts are closely surrounded by an anterior, gullet-like invagination, posterior to which the blepharoplasts rest adjacent to the nucleus. The four flagella extend 20 to 25 μ beyond the anterior limit of the pocket. Detailed descriptions of the morphologies of the ameboid and flagellate phases are given to supplement the morphology described by Whitmore. Possible affinities to other amebo-flagellates are discussed. It is concluded that the organism is generically and specifically distinct; and while its name is erroneously descriptive of its flagellate phase, it is taxonomically valid.

Notes: SYNOPSIS. The organism used in the experiments fits Pierson's satisfactory description for Euplotes eurystomus. The mating behavior of 90 stocks of E. eurystomus collected from west Japan was studied. Mating occurs only after a decline in nutritive conditions. When the stocks were mixed together, two at a time, in all possible combinations, mating took place in all the mixtures. Mating occurs in the evening or the morning after mixing. An agglutinative reaction does not precede mating; but before pair formation, characteristic pre-pairing behavior is observed. Selfing is found in all the stocks, usually after the log-phase of the growth curve. Culture fluids from various cultures have no detectable capacity to induce selfing, but some of them can suppress selfing. The latter occurs only in specific combinations. Controls mixed with distilled water instead of culture fluid always contain selfers. From the results of such experiments, it is possible to classify the stocks into 9 types, so that stocks of the same type have the same character with respect to suppression of selfing. The culture fluid from type II suppresses selfing only in animals of type I, type IV acts only on type III, VI on V, VIII on VII, and VII on both V and VI. The reciprocal actions also occur, i.e., fluid from I suppresses selfing of type II, etc. The origin of the two mating members of a conjugating pair was traced by making mixtures of normal animals of one type with morphologically abnormal animals of another type. The latter have a distinct swelling at the left margin of the body. Such mixtures (I × II, V × VI and VII × VIII) yield conjugating pairs of normal mated with abnormal animals, i.e. cross-conjugating pairs, in 86–94% of the animals. Mixtures of type VI with VII yield a smaller percentage (48%) of cross-conjugating pairs. Mixtures of two cultures belonging to the same type, (II × II, VI × VI and VIII × VIII), in which selfing is not suppressed, yield 42–50% conjugating pairs of normal with normal, (selfing of the normal culture), and 32–45% conjugating pairs of abnormal with abnormal, (selfing in the abnormal culture). Mixtures of two cultures belonging to diverse types in which selfing is not suppressed (I × V, I × VIII, II × III, II × VII, II × IX, III × V, III × VI, III × VIII, IV × VI and VI × IX), yield 36–48% conjugating pairs (selfing) of normal with normal, and 26–50% conjugating pairs (selfing) of abnormal with abnormal. Interbreeding between two types thus normally occurs only when culture fluid of each type inhibits selfing by animals of the other type. These two types, which interbreed freely, may be considered as complementary mating types. The mating types of E. eurystomus thus fall into 5 varieties so that each one (except the fifth) has two complementary mating types. The mating types are numbered I and II in variety 1, III and IV in variety 2, V and VI in variety 3, VII and VIII in variety 4, and only IX in variety 5. Intervarietal mating does not occur in many combinations, but exceptionally it occurs between types V and VII, and between VI and VII. These hybrids become senile and finally die.

Notes: Books reviewed in this article:Larwood, G. & Rosen, B. R., eds. 1979. Biology and Systematics of Colonial Organisms.Hellebust, Johan A. & Craigie, J. S. eds. 1978. Handbook of Phycological Methods. Physiological and Biochemical Methods.

Notes: SYNOPSIS. Surface saccharides in 2 Trichomonas vaginalis strains, the moderately pathogenic, JH34A, and the mild, JH162A, were analyzed with the aid of plant lectins. Concanavalin A (Con A), wheat germ agglutinin (WGA), soybean agglutinin (SBA), castor bean agglutinin (CBA), and lectin from the garden pea (GPA) were employed in agglutination tests and in treatment of ultrathin sections for electron microscopy according to the horseradish peroxidase-3,3′-diaminobenzidine method. With Con A and WGA, small quantitative differences were noted between the 2 strains in the results of agglutination and in the reaction-product deposits observed by electron microscopy. Distribution of the binding sites for the 2 lectins was also somewhat different in the JH34A and JH162A trichomonads. In general, the reactions with the more pathogenic strain were slightly stronger. Although the reactions with SBA and CBA lectins were weaker than those with Con A or WGA, they provided the means for qualitative differentiation between the 2 trichomonad strains. SBA alone agglutinated the JH34A strain and formed demonstrable deposits on the cell surfaces. On the other hand, only CBA reacted with JH162A flagellates. The garden pea lectin failed to bind to the surface of either strain. On the basis of results obtained with the control preparations incubated in the presence of specific inhibitors, it was concluded that both strains had α-methyl-D-mannoside and/or α-methyl-D-mannoside-like as well as N-acetyl-D-glucosamine residues on their surfaces. In addition, JH34A strain had D-lactose-containing residues while JH162A trichomonads had residues with D-galactose. Neither strain appeared to possess residues containing N-acetyl-D-galactosamine.

Notes: SYNOPSIS. Centrifugation for 30–40 seconds at 8,000 g has been used to render monopodial specimens of the large free-living ameba. Chaos carolinensis. These monopodial amebae exhibit obvious torsional movements in the tail. In many cases the posterior ectoplasm assumes the form of a screw with helical ridges forming in place of the more common straight dorsal fins. This finding prompted a re-examination of normal polypodial C. carolinensis, and a majority of these were found also to exhibit torsional movement in the tail and in retracting pseudopodia. These movements suggest that the cytoskeleton of Chaos may have a helical component in its organization.

Notes: Books reviewed in this article:Levandowsky, M. & Hutner, S. H., eds. Biochemistry and Physiology of Protozoa.Raymont, John E. G. with J. D. Burton & K. R. Dyer. 1980. Plankton and Productivity in the Oceans. Vol. I. Phytoplankton.

Notes: Book reviewed in this article:Maramorosch, Karl & Hirumi, Hiroyuki, eds. 1979. Practical Tissue Culture Applications.

Notes: SYNOPSIS. Cysteine and ascorbic acid were previously shown to be required by Entamoeba histolytica trophozoites for attachment to glass, elongation, and ameboid movement as well as for short-term (12–24 h) survival in a balanced salt solution containing bovine serum albumin and a vitamin solution (Maintenance Medium 1). If the only function of cysteine and ascorbate was to decrease the redox potential, other reducing agents should be effective. However, the requirement for cysteine in the presence of ascorbic acid was highly specific. Equally effective were D- and L-cysteine; however, of many other compounds tested, only thioglycolic acid, ascorbic acid, or L-cystine (in decreasing order) were somewhat active. Under N2 atmosphere, cysteine and ascorbic acid were still required, although their concentrations could be halved. The ability to attach in the maintenance medium was irreversibly lost after only 5 min of cysteine-ascorbic acid deprivation; however, there was no decrease in viability when the amebae were transferred to growth medium within 30 min. Cysteine thiol groups in the medium were oxidized rapidly regardless of the concentration of ascorbic acid or the presence of amebae; however, ascorbic acid prolonged attachment of amebae.

Notes: SYNOPSIS. Low concentrations of chlorpromazine (∼0.01 mM) inhibit growth and nucleic acid synthesis in the ciliate Tetrahymena pyriformis. Brief exposure of the cells to, e.g. 0.018 mM chlorpromazine, had very little effect on 14CO2 production or on label incorporation into glycogen from [1-14C]glucetate, [6–14C]glucose, or [1-14C]leucine, but 17-h exposure of stationary phase cultures to this drug caused marked alterations in metabolism, including an almost complete loss of ability to decarboxylate L-[1-14C]leucine and L-[1-14C]tyrosine. It was shown that loss of ability to decarboxylate these amino acids results from loss of ability to transport them.

Notes: SYNOPSIS. A survey of 41 herbivorous mole-rats, Spalax ehrenbergi Nehring, in Urfa, Adiyaman, and Maras provinces of Turkey revealed 7 new species of Eimeria in addition to previously described Eimeriidae. The shape, average dimensions (in μm) of their oocysts, and the numbers of hosts from which the new species were isolated were as follows: Eimeria urfensis sp. n., ellipsoidal (33 × 21), from 8 hosts; Eimeria adiyamanensis sp. n., ovoid to ellipsoidal (33 × 18), from 6 hosts; Eimeria haranica sp. n., elongate ovoid (37 × 20), from 22 rats; Eimeria marasensis sp. n., ellipsoidal (36 × 18), from 2 rats; Eimeria oytuni sp. n., pear-shaped (24 × 17), from 2 hosts; Eimeria celebii sp. n., ellipsoidal (16 × 9), from 1 rat; and Eimeria torosicum sp. n., spherical to subspherical (11 × 10), from 2 animals.

Notes: Defined media are described that support 14-20 h generation times for Acanthamoeba castellanii and A. rhysodes in monolayer cultures. the media differ in minor ways from previously described media, but the growth rates are greatly improved over previously reported values. Maximum growth rates were observed for A, castellanii in a complex medium containing 21 amino acids, but near-maximum rates could be achieved in relatively simple media containing 9 amino acids. Growth occurred with 6 amino acids, as reported by others, but generation times exceeded 30 h. Amitosis was a common problem during early subcultures in defined media, but became infrequent after repeated transfers. Synchronous encystment resulting in 70-80% cyst formation could be induced in the defined media by glucose and acetate starvation. the rate of encystment varied with cell density at the time of starvation and was optimal at initial densities of 400-800 amebae/mm2.

Notes: Tetrahymena pyriformis strain HSM secretes 4 isozymes of hexosaminidase. Purified isozymes B1 and B2 are eluted from the void volume of a concanavalin A-Sepharose column, suggesting that they are not glycosylated. Purified isozymes A1 and A2 bind to the column and are eluted at ∼0.1 M α-methylmannoside, suggesting that these isozymes are glycoproteins. In agreement with earlier deductions based on a differential kinetic assay for the A and B isozymes, the elution pattern of hexosaminidase activity from material secreted by cells grown to early and late stationary phase was consistent with these secretions containing primarily the B and the A isozymes, respectively.

Notes: The surface proteins and glycoproteins on red cells from normal and Babesia bovis-infected calf blood have been compared. Several radiolabeling probes were used to label specifically external membrane molecules which were then separated by sodium dodecyl sulfate-polyacrylamide gel electrophoresis and identified by autoradiography or fluorography. No differences were observed among the Coomassie Blue-stained membrane proteins of erythrocytes from individual uninfected calves. Comparison of red cells from these animals also indicated no qualitative differences in the surface proteins with accessible tyrosyl residues labeled by lactoperoxidase-catalyzed radioiodnation, although some quantitative variation in the uptake of radioactivity into particular proteins was observed. the major radioiodinated bands on normal bovine erythrocytes had Mr of 165, 130, 90, and 45 kiloDaltons. However, labeling of surface glycoproteins by the periodate/[3H]NaBH4 and galactose oxidase (± neuraminidase)/[3H]NaBH4 methods showed significant differences in the surface proteins of red cells from individual uninfected calves. of 14 animals tested, 5 had major labeled glycoproteins of unique Mr. No changes were observed in radioiodinated surface proteins of total red cell samples from infected calves with 0.5-6% parasitemia. Radioiodination of concentrated infected red cells from the same samples (concentrated by selective hypotonic lysis of uninfected erythrocytes in KC1) resulted in the labeling of 3 new surface proteins, with Mr of 118, 115, and 60 kiloDaltons. the same new 125I-labeled bands were identified on infected cells from 3 avirulent strains of B. bovis used in vaccine production. Furthermore, in concentrated infected cells there was very poor radiolabeling of major bands strongly labeled on uninfected cells (Mr 165, 130, and 90 kiloDaltons), suggesting parasite-induced loss of these proteins. Although there were some differences in 3H-labeled surface glycoproteins of red cells from normal and. B. bovis -infected blood, they were restricted to minor labeled bands and were not seen consistently. the labeled surface glycoproteins of concentrated infected cells were very similar to those of the uninfected red blood cells from infected blood.

Notes: SYNOPSIS. Two methods for purifying balantidia are described. The first one may be applied to cultures which are not thriving when it is desirable to keep the purified ciliates without loss in number. Another method may be used for bulk material such as intestinal contents containing these ciliates.