ALBERT

Notes: SYNOPSIS. Experiments were performed to ascertain the effect of heat and cold on oral and micronuclear development in synchronized Tetrahymena pyriformis WH-6. The developing oral primordium becomes insensitive to cold sometime during stage 2. Cold shocks cause the reversion of many stage 2 primordia to stage 1. Cells so affected are set back in division. The delayed division is always asynchronous. When heat shocks are applied prior to late stage 4, the developing primordium will regress. High temperature shocks applied at later stages permit continued development. However, when the cell begins to cleave at the high temperature, division is frequently arrested and the new oral areas regress. Subsequent cell separation is greatly delayed and asynchronous.Heat and cold affect the micronucleus in the same way. Both agents prolong the arrest of mitosis brought about by the synchronizing treatment. A temperature shock is ineffective if applied after there is a space completely separating the chromosome groups, so that mitosis is completed in the presence of the agent. Bimicronucleate chains result in those cases in which division is arrested by heat shocks.It is suggested that the different phases of sensitivity to heat and cold may reflect different types of syntheses necessary for development of the oral primordium. Division arrest and subsequent oral replacement might possibly be related to high temperature induced changes in the physical state of the ciliate cortex.

Notes: SYNOPSIS. The free amino acids of E. invadens and 4 strains of E. histolytica cultured in the CLG medium have been identified by thin layer chromatography. The chromatogram patterns of 3 strains grown for 72 hr at 37°C (103, K-9 and 200) were nearly identical. Amino acids detected on chromatograms according to Rf values, relative positions on chromatogram plates, and identifying colors using a polychromatic ninhydrin spray were: leucine/isoleucine, tyrosine, valine, alanine, glycine, glutamic acid, lysine/ornithine, histidine, proline, plus very small amounts of arginine and possibly serine, aspartic acid and citrulline/glutamine. Cysteic acid may also be present. The same amino acids were detected on chromatograms using comparable extracts of strain Laredo and E. invadens grown for 6 days at room temperature. However, the patterns were different in that serine, glycine, threonine and especially alanine were present in greater abundance in these latter 2 cell types.These chromatogram patterns were compared with similar analyses of strains Laredo and 200 grown in the modified Shaffer-Frye medium of Reeves.Similar analyses are reported on the basic ingredients of the CLG medium, including the cells and protoplasts of the Bacteroides, the non-multiplying bacterial associate employed in the CLG medium. The chromatogram patterns of the Bacteroides, protoplasts and medium were decidedly different from those of the amebae, thus indicating that adequate separation of bacteria, amebae and medium was accomplished.Analyses of the culture filtrates of all cells analyzed revealed a possible difference between the Laredo strain and the other strains of E. histolytica (103, K-9 and 200) in amino acid utilization. Similar differences were observed between the Laredo strain and E. invadens.

Notes: SYNOPSIS. Colligocineta furax gen. nov., sp. nov., parasitizes the epithelial cells of the peristomial cirri of the sabellid polychaete Laonome kröyeri Malmgren. The material studied was dredged in West Sound of Orcas Island, San Juan Archipelago, Washington. In general, the pattern of ciliation of Colligocineta resembles that of Hypocomella and Heterocinetopsis. However, of the ten kineties which constitute the ciliary system, two from the extreme right side appear to be continuous with two from the left side. During division, the posterior part of the ciliary field is conferred upon the opisthe, and in the proter all of the ten kineties are for a time completely separate.

Notes: SYNOPSIS. Myxosoma cartilaginis n. sp. is described from the cartilage of Lepomis macrochirus (bluegill), L. cyanellus (green sunfish) and Micropterus salmoides (largemouth black bass). The development of the parasite is described from naturally infected fish which were held in spore-free water after infection. The sporoplasm invades cartilage, and becomes a multi-nucleate trophozoite which forms pansporoblasts, each of which produces 2 to 4 spores. The first spores appear in 7 weeks.The histopathology in the above fish consists at first of little cellular reaction, but after 4 to 5 months epithelioid granulomas appear around some of the spore masses. Cartilage liquefaction is present around the parasites for at least 5 weeks. Eosinophilic globules are present in cartilage cells adjacent to the lesions. Diffuse infiltration of the spores from the lesions is described.Of 24 chemicals tested for polar filament extrusion, potassium hydroxide gave the best results.An illustrated synopsis of the Myxosoma of North American fishes is given. Included is some additional information and illustrations of M. hoffmani Meglitsch, 1963. Also included is a table showing the hosts, site of infection, geographic location, spore and polar capsule sizes.

Notes: SYNOPSIS. Two species of hysterocinetids occur in the alimentary tract of Drilocrius breymanni, an aquatic oligochaete collected in Departamento del Valle, Colombia. The suckers of both species are unusual for their complexity. In Craticuloscuta escobari gen. nov., sp. nov., the sucker is a shallow oval concavity with longitudinal and transverse supporting elements. About one-fifth of the area of the sucker, in its posterior portion, is ciliated, but argyrophilic punctations, which probably represent kinetosomes, are distributed in a regular pattern over most of its surface. In Epicharocotyle kyburzi gen. nov., sp. nov., the oval major portion of the sucker is deep, and continuous with a short trough which extends posteriorly and bends toward the left. Veil-like flanges, bordered by a fringe of thick, inactive cilia, arise from the margins of the sucker on either side. In the region of the trough, the flanges may overlap in such a way that the trough is almost completely covered. The trough and a small area of the major portion of the sucker anterior to it are ciliated. However, argyrophilic punctations which probably represent kinetosomes are distributed over most of the surface of the sucker. The pattern of longitudinal and transverse supporting elements found in the sucker itself extends into the flanges. In both Craticuloscuta and Epicharocotyle, the arrangement of the adoral and buccal ciliary organelles is essentially like that in Hysterocineta, Ptychostomum, and other ciliates of the family Hysterocinetidae.

Notes: SYNOPSIS. Various protozoa and lower metazoa were exposed to filtrates of Staphylococcus aureus B (formerly called Type S-6) (2) and non-enterotoxigenic filtrates of staphylococci to study the toxicity of staphylococcal enterotoxin to these organisms. No reaction specific for enterotoxin was observed either in those culture filtrates from toxin-producing strains or in solutions of purified enterotoxin. Non-specific reactions were obtained with various growth media and a “potassium inhibited” filtrate containing 0.5% K2HPO4.

Notes: SYNOPSIS. The effect of hexamethonium chloride, an acetyl-choline competitor, on the ciliary and myonemal systems of Spirostomum intermedium and S. ambiguum was investigated. Although the drug caused immobilization of the cilia, severe cell damage often ensued indicating an unspecific action. The general reaction was usually more severe and the ciliary inhibition less in S. ambiguum than in S. intermedium. It is postulated that the general reaction is the result of either membrane depolarization or binding of hexamethonium at the surface. Fed animals were more susceptible to drug action than starved ones. Raising the external potassium level did not affect the drug action.

Notes: SYNOPSIS. A morphological study on the ectoplasm and the proboscis in the ciliate Didinium nasutum, has been performed by means of an electron microscope. The ectoplasm and the endoplasm of Didinium are separated by a fibrous layer. In addition to the ciliary apparatus and the filament system, the ectoplasm is characterized by having ectoplasmic vacuoles enclosing cross-striated bodies and by having small rods surrounding the ciliary basal body.The filament system is composed of 4 types of tubular filaments: primary filaments originating from the basal body, secondary ones coursing longitudinally along the cell periphery, tertiary ones going down in cylindrical arrays from the periphery of the proboscis into the endoplasm, and finally kinetosomal ones from the base of the basal body into the endoplasm through the newly found pore of the fibrous layer.The fine morphology of the trichites in the proboscis is elucidated three-dimensionally and illustrated schematically. Moreover, the correlation among the small rod, ectoplasmic vacuole and trichite is discussed.

Notes: SYNOPSIS. Animals arising spontaneously in a culture of Paramecium aurelia, variety 4, strain 51.8s, swam about three times as rapidly as normal 51.8s, 51.7s or 29.8 animals. When the 51-fast animals were mixed with 51.8 or 29.8 paramecia, a random sampling of swimming rates showed a bimodal distribution. The faster rate of 51-fast animals was maintained under such deleterious conditions as 48-hour starvation. “Fastness” or “slowness” could not be selected for in vegetative clones. The 51-fast paramecia would not mate with 51.7, 51.8 or 29.8 animals, although fission rate, serotype and general appearance indicated that 51-fast probably arose from strain 51.8.

Notes: SYNOPSIS. Silver stains of the free-swimming sessiline peritrich Opisthonecta henneguyi reveal the adoral infraciliature as the bases of two membranes, a haplokinety and a polykinety, which diverge at the buccal overture and spiral down the infundibulum to end at the cytostome. A second polykinety parallels the adoral polykinety in the oral half of the infundibulum, and the two form a peniculus. The haplokinety appears as a single row of kinetosomes, the adoral polykinety as a series of transverse rows of three kinetosomes. The peniculus is six kinetosomes in width.The electron microscope shows that the haplokinety is a double row of staggered kinetosomes. Only the external row bears cilia. The polykinety is a complex ciliary membrane, three kinetosomes wide. The three kinetosomes are connected with one another by fibrous bundles passing beneath them. They are linked orally and apically into longitudinal rows of thick, zig-zag, fibrous connections. The kinetosomes of the internal longitudinal row are attached by a dense fiber to a strand of fibrous material interrupted at regular intervals by dense nodes.A section of the wall of the infundibulum is thrown up into longitudinal folds with tubular fibrils running parallel to the folds. These structures, the crests, appear to continue into the cytopharynx. Beneath and around the adoral and infundibular infraciliature and the crests is a fibrous matrix with dense nodes, resembling the reticulated infundibular fiber described by Faureé-Fremiet.The trochal band in silver stains appears as short diagonal rows of kinetosomes. The electron microscope shows 5 to 7 kinetosomes per diagonal row. The kinetosomes of the diagonal rows are linked to thick dense rods which originate just above the trochal band and continue antapically past the kinetosomes for a distance of 10 to 15 μ. The kinetosomes are joined to one another by fibrous strands and each is also connected by a dense fiber to the diagonal rod to its left. Running below the kinetosomes and at right angles to the rods is a system of striated fibers.At the aboral end of the body, a ring, 2 μ in diameter, of argentophilic granules is shown by the electron microscope to be a small circle of kinetosomes. Sessile stages have not been reported for Opisthonecta. The aboral ring is probably a vestigial or non-functioning scopula.The argyrome is represented by circular striae around the body. Each stria bears argentophilic dots on either its apical or its antapical side. Electron microscopy reveals that these dots are pores in the cuticle. The striae themselves may be points of adhesion between the inner cuticle and the outer cuticle, or ridges of cytoplasm between flattened alveoli of the inner cuticle. A dense fiber runs below and parallel to each stria. Opisthonecta shows at least three different kinds of ciliary membranes. Some speculations are offered on the taxonomic affinities of peritrichs based on their infraciliature.

Notes: SYNOPSIS. Haplosporidium mytilovum Field, 1924, a sporozoan (?) parasite in the ova of the mussel Mytilus edulis L., is found to be morphologically similar to, and deemed to be congeneric with, the type species of genus Chytridiopsis Schneider, C. socius S., 1884, in beetles. It is compared also with the only other reported species of Chytridiopsis in a mollusc, C. ovicola Léger and Hollande, 1917, in ova of the European oyster, Ostrea edulis L. These two parasites in ova of bivalve molluscs are much alike but, since they seem to have some slight morphological differences, it would be premature to conclude that they belong to the same species. Chytridiopsis, a genus of uncertain affinities, has been considered by various authors to be related to the Chytridiales, the Haplosporida, the Mycetozoa or the Microsporida. New evidence favors the hypothesis that it is microsporidian in nature, although proof in the form of a clearly demonstrated polar filament has not yet been produced.

Notes: SYNOPSIS. Leptomonas costoris n. sp. is described from Gerris comatus. It differs from other species of Leptomonas in the structure of the reservoir which has ultramicroscopic thickenings in its wall, matched by corresponding thickenings in the adjacent flagellar membrane. The one or two diagonal lines seen in the reservoirs of Giemsa-stained specimens are thought to be manifestations of these ultramicroscopic fibrils. The reservoir structure suggests a close relationship between this species and Cryptobia, (family Bodonidae) in which somewhat similar structures have been described. Blastocrithidia veliae is redescribed and differentiated from B. gerridis.

Notes: SYNOPSIS. Glucose-6-phosphate dehydrogenase activity and the level of reduced glutathione were assayed in host-parasite interactions in which the malaria parasites preferentially invade: 1. mature erythrocytes (Plasmodium lophurae in the duck) and 2. reticulocytes (P. berghei in the mouse). Assay for glucose-6-phosphate dehydrogenase was by the dye decolorization test of Motulsky and Campbell. In P. berghei infected mouse erythrocytes with parasitemias ranging from 28–78% there was no deficiency in enzyme except at the 78% level. Similarly, P. lophurae-infected duck erythrocytes with parasitemias of 29–114% showed no enzyme deficiency except above the 80% level. No linear relationship existed between parasitemia and enzyme level. The reduced glutathione stability test of Beutler in duck erythrocytes infected with P. lophurae in the range 27–67% showed no glutathione instability.

Notes: SYNOPSIS. Axenic cultures of Tetrahymena pyriformis W were used to obtain fractions rich in kinetosomes by alcoholdigitonin extraction techniques followed by centrifugation. The morphology of the kinetosomes was examined in the electron microscope at various stages during the isolation procedure, and compared to the morphology of the in situ kinetosome. In the latter preparation the well known cartwheel structure was present, and in addition 9 electron dense dots were displayed at the end of each spoke of the cartwheel.The prepared kinetosomes could easily be identified during the entire process, and there was no apparent change until after the digitonin step. However, with the further fractionation, alteration was found to have taken place in the interior and in the kinetosome wall. The inside appeared “empty,” and we were not able to find 9 triplets in the wall but only doublets.In view of the morphological alterations in the kinetosomerich fractions, chemical analysis still appears to us to be premature.

Notes: SYNOPSIS. Excystment of Didinium nasutum is solely dependent upon dense bacterial populations and is independent of the type of medium in which the bacteria have been grown. Beers' hypothesis of the need for a factor from proteose-peptone is thereby not confirmed, but the need for living, intact bacteria as postulated by him is fully shown. The process of excystment is initiated by bacteria, but their presence is not required throughout the excystment. Axenically grown paramecia, shown to be adequate as food organisms for didinia, will not induce excystment. Five types of bacteria including Gram-positive, Gram-negative, aerobic and anaerobic all suffice to induce excystment, suggesting that the initiation of this process is caused by some general metabolic process or product of bacteria.

Notes: SYNOPSIS. About 50% of the amoebae found in early prophase through metaphase stages of mitosis have at least some mitochondria (ca. 25%) that contain complex internal structural patterns. These patterns are less frequently seen in mitochondria after metaphase, and they are extremely rare or absent during interphase. In the most typical pattern, larger than normal tubules are arranged in a parallel zig-zag configuration with a small amount of matrix between them. Complex patterns typically comprise about 30% of the mitochondrion; they are usually confined to one area, the remaining portion consisting of a clear matrix with few, if any, peripheral tubules.

Notes: SYNOPSIS. Examination of feces obtained from wild-trapped woodchucks, Marmota monax, near Chambersburg, Pennsylvania, revealed three previously described species: Eimeria monacis, E. perforoides, and E. os. In addition I found a new coccidium, E. tuscarorensis n. sp., described in this paper. Structurally the new species resembles E. wisconsinensis and E. bilamellata. An unidentified polysporocystic coccidium, possibly the genus Klossia, was found in small numbers in one sample.

Notes: SYNOPSIS. Laboratory cultures of the boll weevil, Anthonomus grandis Boheman, became infected with Mattesia grandis n. sp. (Neogregarinida, Ophryocystidae). The ensuing epizootic resulted in destruction of the weevil colony. Infection occurred per os in larval and adult weevils. Sporozoites penetrate the intestinal wall and infect adipose tissue cells. Micronuclear schizogony with production of merozoites is the primary method of multiplication and spread to new foci. Micronuclear schizonts may grow as large as 30 μ in size and produce up to 200 or so merozoites, which may be 20 μ long and 1–2.5 μ wide and are motile. Macronuclear schizonts are formed from these 1st schizogony merozoites, and can become 20–30 μ in size, producing up to 80 or so macronuclear merozoites. These can be 15 μ long but 2–3 μ wide with limited motility. Second schizogony merozoites form gamonts, which pair, forming gametocysts. Nuclear division occurs, resulting in 4 equal sized nuclei and 2 pairs of residual nuclei. Four gametes are formed by cytoplasmic constriction around the nuclei. The gametes rapidly pair to form 2 zygotes in the gametocyst, resulting in 2 spores. Nuclear pairing in 1 of the 2 zygotes often lags slightly behind. Abnormal development of zygotes was rare, but could result in 1 spore with 3 poles and a normal spore, or with only 1 spore developing. Near maturity gametocysts are about 12.5 μ long and 14.0 μ wide, with the gametocyst wall tightly stretched over the poles of the spores. Spores often are slightly flattened on the adjacent side in the gametocyst but frequently attained evenly curved walls on all sides after release. The spores are octozoic, with sporozoite development occurring after release from the gametocyst. Spores measured 7.1 μ X 11.8 μ. Characters are given to separate M. grandis from other species of Mattesia.

Notes: SYNOPSIS. Broad scope investigations have allowed a study of the intestinal parasitic protozoa of the Kenya baboon Papio doguera in its natural habitat as well as an opportunity to follow the intestinal protozoan populations in these primates held in captivity. Samplings indicate that the amoebae found in the baboon are essentially the same as those which commonly occur in man. Balantidium coli is frequent in wild baboons but is self-limiting in animals after a few weeks in captivity. The flagellates Chilomastix mesnili and Giardia lamblia were detected in captive but not in wild baboons; the presence of the latter constitutes a new record for Papio doguera.

Notes: SYNOPSIS. Experimental observation of the pathogenicity of some strains of Hartmannella plus the observation of human meningo-encephalitis due to small amebas which had a structure compatible with that of Hartmannella in the tissues has suggested the concept of respiratory amebiasis followed by cerebral and other complications.Until recently no cultural evidence was available to identify positively the amebas in the human cases. This report summarizes the isolation of Naegleria sp. (HB-1) from human spinal fluid by mouse inoculation followed by tissue culture of the infected mouse brain. C. Butt and his associates, who submitted this material to us, isolated the Naegleria on agar medium with Escherichia coli without antibiotics at 37 C.The new isolate failed to grow on the medium previously suggested by us for Hartmannella. HB-1 is virulent for laboratory animals and has a structure in the tissues which more resembles the amebas in the human tissue than the amebas in experimental Hartmannella infections of mice. Naegleria and Hartmannella are both potential pathogens for normal animals and man. A clinical laboratory method to detect Naegleria as well as Hartmannella is herein suggested.

Notes: SYNOPSIS. Reticulocytosis, stimulated by the destruction of red blood cells by phenylhydrazine, altered the course of infection of both Plasmodium chabaudi and P. berghei in the mouse. P. chabaudi, lacking a preference for reticulocytes, was adversely affected when young cells were present in abundance. Parasitemias diminished and most of the animals survived the otherwise fatal infection. P. berghei preferentially invaded reticulocytes to the extent that the parasitemia became contained largely in the reticulocyte population. This was accompanied by a delay in time to death.

Notes: SYNOPSIS. Uronema nigricans, a hymenostome ciliate, is redescribed by modern technics. Anatomic studies were made on 4 strains treated primarily with the Chatton-Lwoff silver impregnation technic. Particular attention was given to the buccal apparatus and its importance to generic assignment in the order Hymenostomatida.

Notes: SYNOPSIS. A hyperparasite probably related to some lower protistan was found in the cytoplasm of Entamoeba suis Hartmann. These were very minute bodies with a central Feulgen-positive dot, the nucleus, and a bordering cytoplasmic ring with an alcian blue-positive reaction. This organism appeared to interfere with the synthesis of DNA & RNA in the host amoeba as reflected in its relative stainability with Feulgen or pyronin-methyl green. The suggestion is that the parasitized amoebic cysts were most likely rendered nonviable.

Notes: SYNOPSIS. Cell-free preparations from Crithidia jasciculata carried out protein synthesis as measured by 14C-leucine uptake (optimum ∼ 10 mM Mg++) and poly U-directed 14C-phenylalanine uptake (optimum ∼ 16 mM Mg++). Characteristics of the system and sucrose density-gradient patterns of ribosomes were investigated. The charging and transfer reactions—the 2 main steps in protein synthesis—were inhibited by stilbamidine, hydroxystilbamidine, pentamidine, quinapyramine (Antrycide), and suramin.

Notes: SYNOPSIS. Cohnilembus verminus, a marine hymenostome ciliate, is described from a culture taken at Eniwetok. Anatomic studies were made on specimens treated primarily with the Chatton-Lwoff silver impregnation technic.

Notes: SYNOPSIS. Eimeria callospermophili was found in 6 species of ground squirrels and the white-tailed prairie dog. The hosts included Spermophilus armatus from Utah and Montana, S. richardsoni from Montana and Wyoming, S. beecheyi from California, S. lateralis and S. variegatus from Utah, and S. tridecemlineatus and Cynomys leucurus from Wyoming. Infections were generally transmissible from each species of ground squirrel to S. armatus and S. richardsoni. Oocysts from C. leucurus caused infections in S. armatus and S. richardsoni. No infections were found after inoculation of E. callospermophili oocysts into least chipmunks (Eutamius minimus), Mongolian gerbils (Meriones unguiculatus), or laboratory rats; however, excystation occurred in these animals. Resistance to infection did not develop in S. armatus, S. richardsoni, or S. variegatus, but did occur after 5 or more infections in S. lateralis. Eimeria callospermophili had little or no effect on the host in S. armatus, S. lateralis, or S. variegatus, but caused bloody diarrhea in severely infected individuals of S. richardsoni.The oocysts had an oocyst residuum consisting of several distinct bodies, which later coalesced to form a large homogeneous body. Each sporozoite had an unusually large refractile body. In experimentally infected specimens of S. armatus the prepatent period and patent period lasted for 5 and 9 days, respectively. Mature 1st-generation schizonts, first seen 2 days after inoculation, had 8–12 merozoites. Mature 2nd-generation schizonts, first seen 3 days after inoculation, had an average of 18 merozoites which were smaller than those of the 1st generation. Mature gametes were 1st seen 4 days after inoculation. Mature microgametocytes were only slightly larger than mature macrogametes.

Notes: SYNOPSIS. The conclusion drawn in 1921 that the large nuclei in the cytoplasmic cortex of Glugea cysts are not vegetative nuclei of the microsporidan but nuclei of the hypertrophied host cell was based on the discovery of early developmental stages in the mesenchyme of stickleback larvae experimentally fed Glugea spores. This observation had been made on serial sections from experiments done in 1912. The intracellular development of the microsporidan could be followed up in this material only thru the 1st stages of schizogony. Renewed infection experiments, done still in 1921 on a much broader basis, have fully confirmed the previous findings, as briefly stated in 1922. On this material, the intracellular development of G. anomala has been followed up in recent years from uninucleate host cells 7 μ in diameter, interpreted as wandering cells in the mesenchyme, until they became macroscopic multinucleate cysts, in which schizogony and sporogony of the microsporidan produced innumerable vegetative stages and spores of Glugea. The details of the developmental processes are described in the present paper.The multinucleate host cell and the intracellular parasites together form one of the symbiotic complexes for which the term “xenom” or “xenoma” has been used by me since 1949. By a sequence of amitotic nuclear divisions, the uninucleate host cell in the Glugea xenomas of Gasterosteus becomes plurinucleate in contrast to the usual structure of other xenomas of fish.Already in 1921, I thought that the host cell in the Glugea xenomas may have phagocytic properties. The observation of accumulation of granules from pigment cells in some of the Glugea xenomas has now verified this supposition.

Notes: SYNOPSIS. Eimeria eumopos n. sp. (Coccidiida, Eimeriidae) from a Colombian bat Eumops trumbulli (Chiroptera, Molossidae) is described. This is the first recorded coccidium in a bat from the western hemisphere, and the sixth bat coccidium species described to date. The unsporulated oocysts in the bat feces are 30.9–24.0 by 28.9–23.2 μ (near 28.8 × 26.1 μ). Their outstanding feature is the pronounced pitting of the thick brownish oocyst wall.

Notes: SYNOPSIS. An electron microscope study of Plasmodium coatneyi in the rhesus monkey supplied information on the fine structure of trophozoites, gametocytes and of the host cell. The trophozoites resemble other mammalian malaria parasites. They do not have typical protozoan mitochondria, but instead a concentric double-membraned organelle, which, it is assumed, performs mitochondrial functions. They feed on the host cell by pinocytosis, engulfing droplets of erythrocytes thru invaginations of the plasma membranes at any region of the cell or thru the cytostome. Digestion of hemoglobin takes place in small vesicles pinched off from the food vacuole proper.Gametocytes can be clearly distinguished into macro- and microgametocytes. Macrogametocytes are covered by 2 plasma membranes, the inner one appearing thicker in some places. The cytoplasm is filled with Palade's particles and has numerous vesicles of endoplasmic reticulum and toxonemes. In microgametocytes most of the inner membrane is thickened, the cytoplasm has few Palade's particles and vesicles of the endoplasmic reticulum and does not have toxonemes.Erythrocytes with trophozoites are irregularly scallop-shaped and have elevated points with knob-like protrusions covered by a double membrane. If these protrusions are sticky they might be in part responsible for clumping and arresting the schizonts and segmenters in the capillaries. The host cell contains numerous Maurer's clefts which in some instances are continuous with the membranes of the parasite suggesting that they might originate from them.

Notes: SYNOPSIS. Mice, segregated in groups according to sex and age from 5 to 21 weeks, and randomly presented, were inoculated in one continuous process with a trypanosome suspension prepared from a Trypanosoma brucei subgroup stabilate of such a dilution that about 50% of the mice might be expected to become infected. No statistically significant difference occurred between groups, either with regard to sex or to age.Significant alterations in the proportions of mice infected did, however, occur in relation to inoculation order. The inoculation process occupied 12–197 minutes after removal of the stabilate from −79 C storage. Essentially, infectivity rose initially to a peak between 30 and 80 minutes, and then fell off, but was not abolished at the end of the experiment.

Notes: SYNOPSIS. Observations were made on the fine structure of Paramecium bursaria and its intracellular Chlorella symbionts. Emphasis was placed on the structure of the algae and structural aspects of the relationship between the organisms.The algae are surrounded by a prominent cell wall and contain a cup-shaped chloroplast which lies just beneath the plasma membrane. Within the cavity formed by the chloroplast are a large nucleus, a mitochondrion, one or more dictyosomes, and numerous ribosomes. The chloroplast itself is made up of a series of lamellar stacks each containing 2–6 or more thylakoids with a granular stroma and starch grains intercalated between the stacks. The thylakoid stacks of mature algae are frequently more compact than those of recently divided algae. A large pyrenoid is located within the base of the chloroplast. It is made up of a granular or fibrillar matrix surrounded by a shell of starch. The matrix is bisected by a stack of 2 thylakoids. Prior to the division of the chloroplast the pyrenoid regresses; pyrenoids subsequently form in the daughter chloroplasts thru condensation of the matrix material and the reappearance of a starch shell. This shell appears to be formed by the hollowing-out of starch grains already present in the chloroplast stroma. Accordingly, in this case, starch moves from the stroma to the pyrenoid.The algae are located thruout the peripheral cytoplasm of the Paramecium. Each alga is located in an individual vacuole except immediately following division of the algae when the daughter cells are temporarily located in the vacuole which harbored the parental cell. Shortly thereafter the vacuole membrane invaginates, thereby isolating the daughter algae into individual vacuoles. Degenerating symbiotic algae are seen; because these are frequently found in vacuoles with bacteria, they are presumed to be undergoing digestion. Due to the conditions of culture these algae could have been either of intracellular or extracellular origin.

Notes: SYNOPSIS. Electron-microscopic observations were performed on 2 species of Volvox, one similar to V. globator, the other to V. aureus. The former has distinct protoplasmic connections in the adult coenobium and specific structures, named “medial bodies,” in the connections just at the intersection with the middle lamella. The medial body is disk shaped, about 800 mμ in diameter, and is composed of 3 parts, 2 dense outer layers and an intermediate less dense zone. In the latter species, the connection and medial body were not seen. On the other hand, it was commonly seen in both of them that in younger, dividing gonidia neighboring protoplasts were connected with each other by protoplasmic bridges. The bridges are undoubtedly formed due to incomplete cell separation in the division of a gonidium. The structural difference in the adult coen***bium between the 2 species emerges just after inversion of the coenobium. In the globator type the medial body appears just after inversion, and the connection remains unruptured all thru life. In the aureus type, it seems that the connections are withdrawn or degenerate immediately after inversion. It is discussed whether protoplasmic continuity is really maintained by the connection or not in the freeswimming coenobium of Volvox.

Notes: SYNOPSIS. Plasmodium lophurae hemozoin (malaria pigment) is a heme-containing protein which is distinctly different from hemoglobin and hematin by immunologic, spectrophotometric, fingerprint, heme-iron, gel filtration, and starch gel electrophoretic analyses. The calculated average molecular weight of P. lophurae hemozoin is ca. 40,000. Hemozoin contains at least 3 antigenic components and shows some indication of cross-reaction with hemoglobin.

Notes: SYNOPSIS. In tryptone media, optimal growth of nonphotosynthetic Euglena gracilis var. bacillaris on glucose occurred with 1% (w/v) glucose at pH 3.5, and required a previous adaptive period in glucose medium.In short term metabolic experiments, glucose uptake was greatly stimulated by small concentrations of tryptone or succinate; effects of shaking suggested that CO2 has a similar stimulatory effect. Glucose utilization was highly dependent on glucose concentration, with an apparent threshold at about 2 mM and increasing steeply with glucose concentration above this value. In tracer experiments, about 90% of the glucose carbon consumed was assimilated, and about 10% released as CO2.Glucose did not stimulate respiration even during rapid glucose utilization. Tracer studies indicated oxidation of endogenous substrates was depressed by an amount which just compensated for the respiration due to glucose.The conditions which allowed rapid glucose utilization by “resting”E. gracilis var. bacillaris were the same as those known previously to be required for growth on glucose. It was therefore concluded that these factors act directly on the main pathways of glucose metabolism.

Notes: SYNOPSIS. Microstome →macrostome transformation in Tetrahymena vorax was induced by suspending microstomes in a transforming principle, stomatin, released by a potential prey, T. pyriformis. It was found that 70–90% of the microstomes formed macrostomes within 7 hours following suspension in this transforming principle. Macrostome formation occurred by the process of oral replacement. This process involved resorption of the microstome oral apparatus and its replacement with a larger (macrostome) one, which arose from an anarchic field that formed behind the resorbing oral area. Ninety-five percent of those microstomes which were destined to form macrostomes were in some stage of oral replacement 195 minutes after their suspension in stomatin. Several commercially produced products were tested over a wide range of concentrations to determine their ability to act as an inducer of macrostomes. Only 2, Trypticase and Bactocasitone, had any activity, and it was too small to be considered really effective. An attempt was also made to destroy the activity of stomatin by using enzymes. RNAse was effective but only in very high concentrations, so it was suggested that this activity might be related to the destruction of RNA within the transforming cell and not related to hydrolysis of stomatin. None of the other enzymes tested had any effect in reducing the activity of stomatin.

Notes: SYNOPSIS. A developmental sequence is proposed for the haplosporidan Minchinia nelsoni Haskin, Stauber and Mackin, 1966, based on study of oyster infections over the past 5 years in Chesapeake Bay. Uninucleate stages develop by nuclear division into multinucleate plasmodia which proliferate in the tissues by plasmotomy. Relatively small plasmodia containing what are considered to be gametic nuclei originate by unequal plasmotomy of large plasmodia. These have been interpreted to aggregate and fuse to form large plasmodia which contain prozygotes. Pairing and fusion of nuclei occur within each plasmodium to produce zygote nuclei (synkaryons) which undergo division, possibly meiotic, to form sporonts. Sporoblasts differentiate into spores with the development of spore walls and opercula. Cystoid plasmodia develop during times of unfavorable conditions. An anomalous but common sequence involving sexuality and mitosis is described, and the occurrence of various life cycle stages within the host thruout the year is discussed.

Notes: SYNOPSIS. Many of the sub-pellicular and infraciliary structures in protozoa have proved difficult to study with standard thin-sectioning technics. When these structures are viewed in isolated and fragmented form, many of the thin-sectioning difficulties are circumvented. Langmuir-trough isolation followed by critical-point drying, as well as thin sectioning, were used in this study to determine the patterns of sub-pellicular microtubules and fibrils interconnecting kinetosomes of membranelles and cirri of Euplotes eurystomus. The fibrillar network in the bases of these ciliary organelles is presented in some detail and apparent variations in pattern are noted. Functional aspects of some of the structures are discussed. With special preparation nearly whole Euplotes may be obtained for study in the electron microscope. Fused cilia were frequently obtained and their ultrastructure was studied.

Notes: SYNOPSIS. A technic is described for the quantitative assay of paramylum content of euglenoid flagellates. The method relies on the alkaline solubility of paramylum followed by treatment with the anthrone reagent. The intensity of the color developed by paramylum is about 14% greater than that developed by an equivalent amount of glucose. The method is sensitive down to about 10 μg.

Notes: SYNOPSIS. The development of three 8-liter and four 12-liter cultures of the photosynthetic dinoflagellate Gonyaulax monilata was followed for 4 months. Weekly estimates were made of population levels of this chain-forming flagellate, along with incidence of cells in chains and toxicity to fish. Guppies (Lebistes reticulatus) were used to assay toxicity. Populations reached a peak when cultures were 3–5 weeks old, declined during weeks 6–10, and tended to stabilize thereafter thru the 17th (final week). The percentage of cells in chains was related to the slope of the population curve; rapidly increasing populations had the highest proportion of long chains, suggesting that incidence of chains is an index of the growth phase in G. monilata. Peak toxicity was not reached until culture populations had been steadily declining for a month, indicating that most toxin is released by autolysis. The reproducibility of culture population and toxicity levels recommend the methods used for future studies.

Notes: SYNOPSIS. The pigments synthesized by Astasia ocellata include α- and ε-carotene, 4-keto-β-carotene (echinenone), and 4,4′-diketo-β-carotene (canthaxanthin); 4-keto-α-carotene, accounting for about half the pigment in the cells, was tentatively identified; a strongly adsorbed keto-carotenoid, accounting for 25% of the pigments and bearing some similarities to astacin, polytomaxanthin and phoenicoxanthin, was also found.

Notes: SYNOPSIS. Blepharisma intermedium was cultured axenically. The organisms were freed of contaminating microorganisms by serial washing in a sterile salt solution. The major nutrients in the various media were: Freshly killed or lyophilized and autoclaved bacteria (Pseudomonas ovalis), yeast extract prepared from Fleischmann's baking yeast or Fleischmann's yeast autolysate, lettuce infusion or stigmasterol, 6 B-vitamins, and phosphate buffer at 2 times 10−3 M. The cultures were kept in the dark at 25 C. Altho the 1st division after transfer into fresh media was delayed, B. intermedium divided in approximately 32 hours thereafter in most of these media.

Notes: SYNOPSIS. The effects of temperatures of 12–18 C on cell division and oral primordium development were investigated in cultures of synchronized Tetrahymena pyriformis GL-C. If exposures to 12 or 15 C were initiated prior to a “transition point,” long delays of cell division were generated. After this transition point, cell division could no longer be substantially delayed by exposure to low temperature. The time of the transition point was somewhat earlier with 15 C than with 12 C treatments. At temperatures higher than 15 C long delays of cell division were not generated regardless of time of treatment.The effects of low temperature on oral morphogenesis were strongly dependent on the stage which was affected. (i) The further development of cells initially in the “anarchic field” stage (stage 1) was immediately blocked at both 12 and 15 C. (ii) Cells initially in the stages of incipient membranelle differentiation (stages 2 and 3) continued to develop at both 12 and 15 C, and formed oral primordia in which all 3 membranelles were clearly differentiated (stage 4). The subsequent progress of these stage 4 primordia depended on the temperature: at 12 C virtually all were resorbed (and cell division was blocked); at 15 C only about 1/3 were resorbed, while the remaining 2/3 completed their development (with the concomitant completion of cell division). (iii) Cells initially in intermediate stages of membranelle differentiation (early stage 4) developed to some extent at 12 C, and then underwent resorpton of oral primordia and blockage of cell division; at 15 C such cells completed their development and division normally. (iv) Cells in which the membranelles and undulating membrane were complete or nearly so (stage 5 and very late stage 4) at the time of the beginning of the cold treatment subsequently finished their development and went thru cell division, even at temperatures as low as 5 C.These results indicate that in addition to a “stabilization point” which occurs shortly before the completion of membranelle development, there is an earlier change in the primordium at the time of the onset of membranelle development, which renders development much less sensitive to direct interference by low temperature.

Notes: SYNOPSIS. Excysted sporozoites of Eimeria meleagrimitis, E. necatrix, E. acervulina, and E. gallopavonis were inoculated into monolayer cell cultures of bovine, ovine, porcine, and human kidney. E. meleagrimitis developed only in bovine embryonic kidney. Mature schizonts were found in the 11th, 16th, and 20th serial passages, but only immature schizonts were in the 4th and 6th passages. E. necatrix developed to mature schizonts in the 3rd, 4th, 6th, 11th, 16th, and 20th passages of bovine kidney and also to immature schizonts in the 175th and 189th passages of PK-15 (cell line porcine kidney). Schizonts, however, did not develop in the 140th and 145th passages of CCI-33 (cloned PK-15). Neither E. meleagrimitis nor E. necatrix developed in the primary, 1st or 2nd passages of bovine embryonic kidney, primary porcine kidney, 45th and 52nd passages of a human embryonic kidney cell line, or in the primary, 5th and 18th passages of ovine kidney. Eimeria acervulina and E. gallopavonis did not develop in any of the cultures. E. meleagrimitis and E. necatrix probably completed only one asexual generation in culture. The structure of mature schizonts of both species differed greatly from those in the natural host. Schizonts of E. meleagrimitis present at 48 hours were small (13–18 by 12–14 μ) and contained only 12–28 merozoites that were 3.2–3.8 μ long. At 48 hours, E. necatrix schizonts were 15–18 μ in diameter or less and contained only 15–20 merozoites (2.0–3.5 μ long); at 96 hours they were 50–70 by 10–35μ and contained either hundreds of small merozoites (2.0–3.5 μ long) or a lesser number of larger merozoites (9–11 μ).

Notes: SYNOPSIS. In heavily endemic collecting sites in Panamá and Colón Provinces, Republic of Panama, 14.7% of Ameiva ameiva and 8.5% of Basiliscus basiliscus were injected with Besnoitia darlingi. Single infected specimens of A. leptophrys and A. festiva were also taken, these being new host species records for this parasite. Infections were found only in the older lizards.Initially, virulence of the lizard parasites for white mice was low but increased with successive mouse passages. Concomitantly, the cyst-forming capacity of the strain diminished with successive mouse passages. No relation between initial virulence of the lizard parasites for mice and subsequent virulence after 16 or 17 mouse passages was recorded.The original description of B. panamensis (a synonym of B. darlingi) is emended on the basis of extensive material to include cyst diameters of 200–500 μ; also, the liver, mesentery, and tunica propria of the testis occasionally contain cysts. Cysts are frequently macroscopic and on the surface of organs so that they can be seen on casual inspection. B. sauriana Garnham, 1966 is a synonym of B. darlingi.

Notes: SYNOPSIS. An electron microscope study of microgametocytes and macrogametes of Eimeria nieschulzi Dieben, 1924 revealed that they lie within vacuoles bounded by a host unit membrane. The vacuole surrounding the microgametocyte contains granular material. The vacuole around the macrogamete is narrower and contains vesicles and membranes. Micropores were seen on the surface of the plasma membrane of microgametocytes and macrogametes. Microtubules were seen in macrogametes. Young microgametocytes and macrogametes have a similar cytoplasmic matrix, mitochondria and nuclei. Glycogen granules apparently develop around vacuoles in both microgametocytes and macrogametes. Glycogen granules were also seen along the margins of parallel bundles of fibers in microgametocytes. As nuclei of the microgametocyte divide, they move to the periphery of the parasite. Three basal bodies, each with 9 fibers in triplet form, develop in association with each nucleus. Microgametes have 2 free flagella and a central short, attached flagellum. Basal granules lie along the outer fibers of the central flagellum. Each microgamete has an elongate mitochondrion in close contact with the nucleus. In macrogametes wall-forming bodies develop in lacunae in the cytoplasm. Smaller dark bodies with areas of low density were also seen. Wall-forming bodies and dark bodies move to the periphery of mature macrogametes.

Notes: SYNOPSIS. In the nearly mature macrogametes of Eimeria auburnensis, the cell membrane is a unit membrane, with underlying and overlying osmiophilic layers usually present. Cup-shaped micropores were occasionally seen. Smaller, V-shaped invaginations were also found in considerable numbers at the surface. At the deepest point, these invaginations were bounded only by a unit membrane. Immediately adjacent to this point, vesicles with homogenous electron-pale contents bounded by a similar unit membrane, were frequently seen. Pinocytosis evidently occurs at the site of these invaginations. Numerous folds of the host cell membrane bordering the vacuole in which the parasite lay extended about 0.1–0.7 μ into the vacuole. These “intravacuolar folds” varied in depth and number in different specimens. In some, the majority of folds had apparently become disconnected from the host cell membrane. A highly developed smooth endoplasmic reticulum occurred in the adjacent host cell cytoplasm. The intravacuolar folds may assist in transfer of nutrients, including membrane material, from the host cell to the parasite. The evidence indicates that in this species of Eimeria nutrients are taken into the parasite primarily as fluids by pinocytosis and possibly other processes.

Notes: SYNOPSIS. Sexual reproduction of up to 50% of the cells from 9 cultures of Stentor coeruleus was observed repeatedly for several months. Photomicrographs were taken of mating pairs, and a number of new observations were made, including the ability of well fed cells (containing food vacuoles) to conjugate, the ability of a high percentage of cells (approaching 50%) in a culture to mate at one time, a more detailed description of the region of cell attachment as viewed from the frontal fields of the partner cells, and the ability of one partner to twist off and leave its oral area attached to the other member of the pair.

Notes: SYNOPSIS. Comparison of RNA molecules between certain protozoa using the technic of nucleic acid hybridisation revealed that there are complementary sequences for ribosomal RNA molecules in the genomes of such cells. Furthermore the genes for ribosomal RNA have been conserved during evolution in this group of organisms. On the other hand, RNA molecules from these protozoa which can be considered to be “messengers” show little in the way of sequence relationships. By utilising the technic of hybridisation it was found that Oxytricha can compete effectively against Paramecium ribosomal RNA for Tetrahymena DNA but the ribosomal RNA sequences of the latter could not compete completely against Paramecium ribosomal RNA for Oxytricha DNA. The result is interpreted to show that different ribosomal sequences were hybridising with each of the DNA samples from Tetrahymena and Oxytricha. A general interpretation of this result in terms of ribosome evolution is presented.

Notes: SYNOPSIS. Strains of Tetrahymena pyriformis, including amicronucleate strain GL and representatives of 9 syngens, have been examined to determine the patterns whereby cortical features vary with numbers of ciliary meridians. The characteristics scored were the positions of the contractile vacuole pores (CVP's), the extent of the area within which CVP's develop, the incidence of supernumerary CVP's, and the number of postoral meridians. Intrasyngenic comparisons were possible in 6 syngens and permitted an assessment of intrasyngenic variation for these characteristics. Only the CVP positions appear to be reasonably constant within syngens in the strains examined. On the basis of this criterion the syngens can be arrayed in an approximate order of 1, 3, 7, 6, 8, 9, 2, 5, GL and 4; the angle formed between the central axis, the stomatogenic meridian and the CVP's is most acute in syngen 1.

Notes: SYNOPSIS. The bionomics of Labyrinthula Cienkowski and the validity of the family Labyrinthulidae Haeckel are reviewed. The structure, physiology (including nutrition), locomotion, ecology, and possible pathogenicity for eel-grass (Zostera marina L.) are discussed. The uniqueness of its gliding motility along slime tracks, lack of phagotrophy, and poorly understood congregation tendencies emphasize the present taxonomic isolation of the group. Further interest attaches to some species because of their steroid requirements.

Notes: SYNOPSIS. Sporozoites of L. simondi were maintained in a viable state for 7 months in liquid nitrogen. Comparison of parasite development initiated with fresh and frozen sporozoites showed a delay in development of each stage studied. Comparisons of prepatency, first elongate gametocytes, peak density of round and elongate forms, anemia and disappearance of megaloschizonts were made. In each phase there was a delay of 2–3 days in ducks infected with frozen sporozoites.

Notes: SYNOPSIS. Ten strains of Acanthamoeba from freshwater habitats were isolated in clonal cultures. Studies were made of trophic structure, nuclear division, cyst structure, some aspects of cytochemistry, and other characteristics. One strain was identified as A. castellanii (Douglas, 1930), one as A. astronyxis (Ray and Hayes, 1954), and 8 as A. polyphaga (Puschkarew, 1913). Strains of Acanthamoeba isolated by other workers were also examined comparatively.The pattern of nuclear division in all strains resembled that in metazoan cells, with the exception that centrioles were never found. Trophic amoebae had a PAS-positive surface outline. Cyst walls were strongly PAS-positive and also gave a positive test for cellulose with zinc chloroiodide.The genus Acanthamoeba Volkonsky, 1931 is re-defined, being distinguished from Hartmannella Alexeieff, 1912, emend. Volkonsky, chiefly by the formation of tapering, hyaline pseudopods (acanthopodia) and by a cyst made up of an ectocyst and a polyhedral or stellate endocyst, with excystment by removal of opercula. Other characteristics found in all strains include a distinctive food cup, the presence of many small refractile globules in the cytoplasm of trophic amoebae, and a cyst wall containing cellulose. The degree of spindle convergence, employed by Volkonsky as a generic criterion, was unusable.Differential diagnoses based principally on cyst structure are offered for A. castellanii, A. astronyxis, and A. polyphaga. The strain previously called Mayorella palestinensis Reich, 1933 is a distinct species of Acanthamoeba.

Notes: SYNOPSIS. Parauronema virginianum n. g., n. sp., a marine hymenostome ciliate is described from the Virginia coast. Structural studies were made on specimens treated with the Chatton-Lwoff silver impregnation technic and on animals observed with the phase microscope. Particular attention was given to the buccal ciliature and its importance to generic assignment in the order Hymenostomatida.

Notes: SYNOPSIS. Large numbers of sessile ciliates were successfully collected in plastic petri dishes with tight-fitting lids, transported in the water-filled dishes without disturbance. Each species within the transparent dishes was identified with a dissecting microscope and the position on the dish surface of each sessile individual was located and recorded on graph paper for further quantitative comparisons. This method was used for numerous experiments on the ecology and behavior of sessile ciliates and their responses to toxins.

Notes: SYNOPSIS. Structure and morphogenesis, and cytochemical data on Cochlodinium heterolobatum, a new species of unarmored dinoflagellate, were derived from living and fixed material from culture. C. heterolobatum is characterized by the torsion of the girdle which descends in a left-hand spiral 1.8 turns; the sulcus having a torsion of 0.8 turn; a sulcus loop in the epicone; a tongue-shaped lobe in the right hypocone; nucleus in the epicone; and a stigma in the left epicone. Trichocysts and behavior of the nucleus during typical and atypical divisions are described in cells from cultures of different ages. A small form with the specific characters was found. Intracellular bacteria were seen and their growth followed in individuals from cultures of different ages. A possible relationship between those bacteria and the accumulation of metabolites inside old cells is discussed.

Notes: SYNOPSIS. Species of sessile Stentor, Vorticella and colonial peritrichs were collected in boxtype plastic petri dishes. Thru a hole in the wall of the dish, various concentrations of mercuric chloride, a standard bactericidal agent, were introduced. Following a 3-hour exposure to the toxicant, the death of the sessile ciliates followed a set pattern with a clearcut toxicity threshold of 0.1–0.5 parts per million with an LD 50 of about 0.25 ppm. Furthermore, the sessile ciliates were not dislodged when the natural pond water in the dish was poured out and replaced with water from other sources. Various responses were elicited by 4-hour exposure to 4 changes of environment. By this procedure, the protozoan community was subjected to new sets of conditions. Such a technic could serve as a method of detecting and assessing water pollution.

Notes: SYNOPSIS. From characteristics of binary fission, conjugation, size and number of micronuclei, body size and incidence of giantism, a Blepharisma isolate hitherto called B. undulans is classified as B. dawsoni sp. nov. Binary fission in B. wardsi differs from fission in B. dawsoni in that the strand connecting the macronuclear nodes is severed; in B. dawsoni the strand persists.

Notes: SYNOPSIS. Experiments with mixtures of latex-tagged cultures of amoebae of strains, species and genera of the Dictyosteliaceae indicate little specificity in engulfment. This is in sharp contrast to the decided specificity for compatibility in completion of morphogenesis in the same organisms. Lack of specificity in engulfment is considered additional evidence favoring engulfment as a normal feeding activity rather than a process associated with syngamy in the cellular slime molds.

Notes: SYNOPSIS. Eimeria colchici sp. n. is described from English pheasants Phasianus colchicus. It has cocysts measuring 19–33.5 (27.4) by 13–21 (16.7) μ, having both micropyle and polar granule. The large 1st and 2nd generation schizonts occur in the glands of the small intestine, 3rd generation schizonts occur deep in the glands of the ceca, and gametocytes occur in the epithelial cells of the ceca. The prepatent period is 6 days. In young pheasants the parasite causes coccidiosis characterized by formation of white cores in the ceca. Mortality is high in experimental infections. Zoalene (0.0125%) in the feed almost completely suppressed the infection; Amprolium (0.0125%) also gave good control, but sulfaquinoxaline (0.0125%) was not so effective. Sulfaquinoxaline, Saquadil and Sulfamezathine in the drinking water controlled mortality, but treatment had to be applied early to avoid weight losses.

Notes: SYNOPSIS. Monolayer primary and secondary cultures of embryonic bovine kidney, spleen, intestinal and testicle cells, and secondary cultures of embryonic bovine thymus, maintained in lactalbumin hydrolysate, Earle's balanced salt solution and ovine serum were observed for a maximum of 21 days after inoculation of E. bovis sporozoites. The sporozoites entered the cells in all of these cultures but underwent development only in primary cultures of kidney and intestinal cells and in secondary cultures of kidney, spleen, thymus, intestinal, and testicle cells. In acellular media, the sporozoites retained motility no longer than 21 hr. In the cell cultures, free motile sporozoites were seen for as long as 18 days after inoculation. Sporozoites entered cells anterior end first; the process of penetration required a few seconds to about a minute. Sporozoites were also observed leaving host cells. Intracellular sporozoites were first seen 3 min after inoculation; they were observed at various intervals up to 18 days after inoculation. In transformation of sporozoites into trophozoites a marked change in size and appearance of the nucleus took place before the change in shape of the body occurred. Trophozoites were first found 7 days after inoculation, multinucleate schizonts after 8 days, and schizonts with merozoites after 14 days. Schizonts containing merozoites were seen only in kidney, spleen, and thymus cells. The mature schizonts were smaller and represented a much lower proportion of the total number than in comparable stages of infections in calves. Schizonts with many nuclei occurred in intestinal cells; the most advanced stage seen in testicle cells was the binucleate schizont. Nuclear and cytoplasmic changes were observed in the infected cells.

Notes: SYNOPSIS. Peritoneal macrophages from hamsters were monolayered on coverslips in Leighton tubes. Twenty-four hours later these were transferred to a perfusion chamber. Leptomonads were added with fresh medium and the infection process observed with the aid of phase contrast. In the perfusion chamber free-swimming leptomonads attached to the macrophage by the tip of their flagella. Shortly after this initial attachment the macrophage extended a narrow pseudopodium around the flagellum which eventually reached and enveloped the body of the parasite. Upon complete envelopment the pseudopod containing the leptomonad was retracted into the central body of the macrophage. When first seen in the granular endoplasm of the macrophage, most of the leptomonads appeared to be surrounded by vacuoles. In most cases these vacuoles disappeared in a few minutes making it difficult to distinguish the parasite from the host cell cytoplasm.Leptomonads also were added directly to Leighton tube cultures, and the coverslips with the adherent macrophages and parasites were removed, fixed and stained periodically during the infection process. In these preparations most of the parasites were in clumps in the vicinity of macrophages. Details of the ingestion of the clumps could not be seen, but occasionally a single organism was seen with its flagellum and part of its body enclosed by an extended pseudopod. Most of the intracellular leptomonads were in large vacuoles. Forms intermediate between elongate leptomonads and LD bodies were surrounded by smaller vacuole-like spaces. The halo-like vacuoles most frequently seen around LD bodies may have been fixation artifacts. Under favorable conditions the leptomonads transformed to LD bodies in 1–4 hours, but it was 48 hours before a population increase could be found.

Notes: SYNOPSIS. Coccidia-free beagle puppies were experimentally infected with a cloned culture of Isospora rivolta oocysts. The endogenous stages were found in the posterior 1/2 of the small intestine, and rarely in the cecum and colon. Maximum numbers of all stages occurred just anterior to the ileocecal valve. Endogenous stages were found in the distal third of the villi, predominantly parasitizing subepithelial cells of the lamina propria; however, stages were occasionally present in epithelial cells. The number of asexual generations could not be determined from their structure, but evidence based on oocyst production suggested that there were at least 2 asexual generations. The schizonts were 17–24 by 12–25 μ and contained 4–24 merozoites, the most common number being 4 or 8. Schizonts with mature merozoites were found as early as 72 hr, but were present in maximum numbers at 96 hr. Merozoites had slender curved bodies and were 10.5–13.4 by 2.3–3.0 μ. Mature gamonts were found by 144 hr. Mature microgametocytes were 13.4 by 8.7 μ and contained 50–70 microgametes. Microgametes had slightly curved tapering bodies (5.8–6.4 by 0.6 μ) with 2 posteriorly directed flagella 11–14 μ long. Mature macrogametes had reticular cytoplasm and a uniformly large nucleus and nucleolus.The prepatent period was 142–146 hr. The patent period was 13–23 days with an average of 19 days.

Notes: SYNOPSIS. Rabbit antisera to strains of different mating types of Chlamydomonas moewusii and to one strain of C. eugametos were tested against strains of C. reinhardti, C. eugametos, and C. moewussi, and against strains of 2 varieties and 6 mutant types of C. moewusii. Technics of double diffusion, absorption, and immunoelectrophoresis revealed marked serological differences between the sexually incompatible, distinct genetic species C. moewusii and C. reinhardti. Less distinct serological differences were resolved between C. moewusii and the so-called “species”C. eugametos, which is sexually compatible with the former, thus reconfirming the conspecificity between the 2 strains as suggested by Gowans. Marked serological differences were noted between C. moewusii and 2 of its varieties (C. moewusii var. tenuichloris and C. moewusii var. rotunda) which constitute 2 additional genetic species because of sexual incompatibility between themselves and with C. moewusii. Wild types and certain mutants of C. moewusii were compared serologically and could be distinguished on this basis. Strains of different mating types as well as certain mutant strains (e.g., paralyzed flagella, flagella-less, twins and monsters) could be differentiated serologically altho differences were often very subtle. Some antigens were common to organisms tested.

Notes: SYNOPSIS. Optimal growth of the colorless flagellate, Astasia longa, in terms of generation time occurred at 25–30 C. Above and below this interval, generation time increased. In contrast, length of the lag phase was constant over a wide temperature range, 18–32 C. At 13 C dry weight of Astasia was 15% greater than at 28.5. Alcohol-ether soluble material accounted for 72% of the dry weight increase at 13, while RNA and protein contents of the cells were the same at both temperatures. Rates of synthesis of dry weight, RNA, protein and lipid per μl oxygen consumed were all reduced at 13 C; however, lipid synthesis was the least affected. Cell division in Astasia was synchronized repetitively by cold (13–15 C) and warm (28.5 C) temperature cycles. Under best conditions, cell division began immediately at the onset of the warm period. Cellular preparations for cytokinesis apparently were at least partially completed in the cold, and raising the temperature released a block to cell division.

Notes: SYNOPSIS. Isolated rumen protozoan species (Entodinium) were incubated in vitro with starch, antibiotics and Na214CO3. 14C-carbonate was incorporated into amino acids of the Entodinium protein. Arginine, aspartic acid, alanine, and glutamic acid had the highest specific activities. Carbonate was incorporated into the TCA-soluble fraction, into cell polysaccharides, and into ether and acetone extracts of TCA-precipitates.

Notes: SYNOPSIS. Light-dependent incorporation of acetate occurs in an obligate phototrophic strain of Euglena gracilis (strain L). Assimilation is into all major biochemical fractions. Acetate does not induce operation of the glyoxylate by-pass as it does in heterotrophic strains; neither does it stimulate oxygen consumption. Acetate will not replace CO2 in phototrophic growth. A number of carbon sources tested would not support growth in the dark, and glucose was not incorporated either in the light or the dark.

Notes: SYNOPSIS. The uptake, distribution and turnover of phosphorus have been studied for the culture form of Trypanosona cruzi. Following exchange reactions, phosphorus was accumulated at an approximate rate of 1.9 μg/108 trypanosomes/hour in Krebs-Ringerphosphate. Of 3.8 mg P/g trypanosomes (wet weight), 60% occurred in acid-soluble, 13% in phospholipid, 22% in nucleic acid, and 5% in phosphoprotein fractions. Acid-soluble and phosphoprotein fractions incorporated P32 more rapidly than phospholipid and nucleic acid fractions, the phosphoprotein fraction having the highest specific activity by 8 hours of incubation.

Notes: SYNOPSIS. Sulfaquinoxaline and ethopabate are 2 chemically distinct types of antagonist of PABA with anticoccidial action. Reversal experiments with PABA and synergism studies with pyrimethamine indicated that both compounds interfered with the PABA-folic acid metabolic sequence. Six pure strains of Eimeria brunetti responded differently to the 2 compounds. The strain most sensitive to ethopabate was one of 2 strains most resistant to sulfaquinoxaline. Conversely, the strain most sensitive to sulfaquinoxaline was unresponsive to the highest doses of ethopabate employed. Hypotheses to explain the differences in biological effects of the 2 compounds were considered.

Notes: SYNOPSIS. Stationary cultures of Ochromonas danica accumulated lipids as they aged. The bulk of the increase in fatty acids was in the unsaturates, particularly the polyunsaturates. The quantity of lipid peroxides (thiobarbituric acid-positive material) also increased with age. Aging was also associated with increase in sensitivity to inhibitory compounds. The implications of lipid accumulation for cell sensitivity are discussed.

Notes: SYNOPSIS. The size of the population of Naegleria gruberi at the time the amoebae are offered the opportunity to become flagellated is not a critical factor in the morphogenesis of this organism. Small populations (1-15 cells) readily become flagellated. Small populations (1-5 cells) washed several times also become flagellated. Clonal populations (25) have been established. All clones yield flagellates under the usual conditions. It is suggested that the physiological state of the amoebae is a factor in determining the number of cells that will undergo morphogenesis at any given time.

Notes: SYNOPSIS. Frame by frame analysis of cinephotomicrographs of the evacuation of the water excretory vesicle of Amoeba proteus shows that this organelle (commonly called the “contractile vacuole”) does not contract as the water is expelled. Instead, pressure exerted by the underlying endoplasmic “gel” pushes the vesicle against the plasmalemma, bulging the latter until a pore opens through it. The cell membrane and apposed vesicular membrane both rupture through the plasmalemmar pore; the fluid rushes out; and the vesicle collapses against and inverts into itself, but does not contract. There is therefore no systole of the vesicle due to any contraction of it. A survey of the literature shows that others who have studied the evacuation of these water excretory vesicles in amebas, suctorians, and ciliates have also described them as collapsing, not contracting. Recent electronmicrographs of a number of protozoa also indicate that the water excretory vesicle collapses, and does not contract as it evacuates its contents; and that there are no fibrils surrounding the organelle which might promote its contraction. We suggest that the term “contractile vacuole” be discarded as a descriptive and identifying term for such organelles; and that they be called “water expulsion” organelles. We further suggest that the term “vacuole,” which implies that the structure is empty, be replaced by the term veside, implying its function as a small container, and that the organelle be preferentially called the water expulsion vesicle. We also suggest that the terms “systole” and “diastole” be discarded and be replaced with enlargement and evacuation so that the erroneous implication of a contraction and relaxation cycle may be dispelled.The succeeding new water expulsion vesicle in Amoeba proteus seldom forms at the site of the old one, but usually forms at a new site in the sol anterior to the gel of the tail region, to which it is transferred prior to expulsion. A tentative suggestion of how this transfer may occur is offered.

Notes: SYNOPSIS. Adenosine triphosphate (ATP) with pyruvate, or adenosine diphosphate with phosphoenolpyruvate, favor the development of Plasmodium lophurae removed from its host erythrocytes and kept extracellularly in vitro. It seemed possible that the parasites might be deficient in enzymes of the glycolytic cycle concerned with the generation of ATP. The ATP content of duck erythrocytes infected with P. lophurae was lower than that of uninfected cells. Infected erythrocytes, however, had somewhat higher contents of both pyruvic kinase and phosphoglyceric kinase than did uninfected ones. Both of these enzymes could be found in the free parasites. Furthermore, the pyruvic kinase of the free parasites was inactivated by freezing and thawing, whereas that of the host erythrocyte was not affected. It will be necessary, therefore, to look further for the basis for the favorable effect of ATP with pyruvate on parasites developing extracellularly in vitro.

Notes: SYNOPSIS. Properties and cellular location of acid phosphatase in Trypanosoma gambiense were studied. Activity was found in both the sediment (32,000 ×g) and the supernatant of homogenates. Cenrifugation in 0.3 M sucrose showed activity principally in the lowspeed fraction (4,000 ×g). One min of sonication released most of this activity. Several phosphomonoesters were hydrolyzed at acid H's. Enzymatic activity was relatively specific for pyrophosphate and p-nitrophenylphosphate at pH 3.6. At pH 5.2, purine and pyimidine nucleotide 5′-triphosphates as well as adenosine di- and ono-5′-phosphates were hydrolyzed nonspecifically. Activity with yrophosphate at pH 3.6 had a temperature optimum of 60-70 C while that for adenosine 5′-triphosphate (pH 5.2) was 50 C. These ctivities of the sediment required no metal co-factors and were inibited by Fe++, inhibition at the lower pH being greater.Glucose 6-phosphate was hydrolyzed by the supernatant with maximum activity between pH 6.0 and 7.2 and a temperature optimum of 50 C. This pH range showed a broad plateau with 2 or 3 minor peaks. The hydrolysis of p-nitrophenylphosphate showed a similar pH curve. In glucose 6-phosphate hydrolysis, Mg++ was a required co-factor but could be replaced by Ni++ or Co++. Ammonium sulfate fractionation precipitated most of the supernatant activity between 50 and 75% saturation.A modified Gomori technic produced spherical deposits of PbS thruout the cytoplasm of the intact cell. With the electron microscope, Pb phosphate deposition was observed in membrane-bound vesicles (i.e., lysosomes) approximately 100-150 mμ in diameter. These organelles were common in the region of the reservoir at the base of the flagellum. Acid phosphatase activity specific for glucose 6-phosphate as substrate was localized within this basal pocket.

Notes: SYNOPSIS. Trypanosoma occidentalis sp. n., a hemoflagellate encountered in the blood plasma of 3 freshwater teleosts, Cottus gulosus, C. rhotheus (Family Cottidae) and Gasterosteus aculeatus (Family Gasterosteidae) from Washington State, is described and recorded. Morphologic and morphometric features are detailed, and comparisons are made with other trypanosomes reported from North American fishes and from related species of teleosts from Eurasia. The relationship of the geographic isolation of parasite, hosts, and potential vector in the determination of the new species is discussed.

Notes: SYNOPSIS. By means of the ninhydrin-Schiff method for proteins a diffuse reaction as well as one localized in granular inclusions can be shown in the cytoplasm of fibroblasts, epithelial cells, and macrophages in trypsin-dispersed chick liver cell cultures. Nuclei and nucleoli also take the specific stain. A progressive loss of cytoplasmic and nuclear staining occurs in the fibroblasts in cultures infected with a relatively pathogenic strain of T. vaginalis. A loss occurs in epithelial cells in advanced stages of degeneration, but in less damaged cells, while the diffuse reaction disappears, the number and staining intensity of the cytoplasmic inclusions remain unchanged or possibly may increase somewhat. The intensity of the diffuse reaction and the number and size of the characteristic inclusions increase in the active, parasite-free, experimental macrophages, but phagocytes with trichomonads closely applied to their external surfaces and those containing the flagellates within their cytoplasm typically retain only a few weak-staining inclusions.Similar distribution of alkaline and acid phosphatases occurs in preparations treated according to Gomori's and Burstone's methods, except that no nuclear staining is obtained with the latter. Activity of both enzymes is localized primarily in inclusions which are dispersed thruout the cytoplasm of fibroblasts and epithelial cells and tend to accumulate along the cell membranes and around the nuclei. In the course of infection with T. vaginalis there is a progressive loss of alkaline phosphatase from both cell types; however, the acid phosphatase activity increases. In the control macrophages both enzymes are localized in mostly rather large, rounded cytoplasmic inclusions. The number of such inclusions increases in the parasite-free experimental macrophages, but only a few weak-staining granules remainin phagocytes with engulfed trichomonads and in those whose external surfaces are in direct contact with the parasites. The loss of the inclusions is less apparent in macrophages containing degenerated flagellates than in the ones with healthy trichomonads, but regardless of the condition of the parasites, the highest enzymatic activity is found around them.ATPase and 5′-nucleotidase are localized in small granules dispersed thruout the cytoplasm of fibroblasts and epithelial cells. The granules tend to accumulate along the periphery of the cells and around the nuclei. A diffuse cytoplasmic reaction is present in preparations processed for 5′-nucleotidase. Nuclei and nucleoli give positive reactions for both enzymes. In the course of infection with trichomonads, activity of the 2 enzymes declines in both culture cell types. Control macrophages have diffuse cytoplasmic reaction for ATPase and 5′-nucleotidase and these enzymes are localized also in rounded cytoplasmic inclusions. Activity of both enzymes increases in the parasite-free experimental phagocytes, but little if any diffuse staining and only a few characteristic inclusions are left in macrophages with engulfed healthy trichomonads and in those whose external surfaces are invested with the flagellates.The ninhydrin-Schiff-positive inclusions found in the macrophages appear to be the same as some of those which have acid phosphatase activity and may well be identical with the glycolipoprotein bodies noted by us previously. On the grounds of their chemical constitution and behavior it seems likely that the inclusions are lysosomes.

Notes: SYNOPSIS. Chilomonas paramecium developed significant resistance to INH at concentrations up to 150 mg/100 ml. Once established, the resistant strains grew subnormally in drug-free medium and were more susceptible than the normal strain to sulfanilamide, but were much more resistant to PABA (10-20 mg/100 ml). In addition, INH-adapted strains were less responsive than the controls in PABA reversal of SA-inhibition. Strains adapted to sulfanilamide, sulfapyridine, and nicotinamide were less resistant to INH than the normal strain.

Notes: SYNOPSIS. The ultrastructure of the herbivorous amoeba Pelomyxapalustris was studied. Nuclear division is not understood in this amoeba, and evidence for the method of nuclear division was sought. This species typically has many spheroidal nuclei which are similar within a given cell. However, some amoebae from our collections differed from this common type in both the number and structure of their nuclei. This suggested stages associated with nuclear division. One current hypothesis of nuclear division in this organism is that of nuclear budding. Our evidence is more in accord with this method than with mitosis.The cytoplasm contained no mitochondria, Golgi bodies, contractile vacuoles or crystals. Most amoebae had 2 types of bacteria (bacteroids or endosymbionts) in their cytoplasm; a separate vesicle enclosed each of these. Characteristically, only 1 type of bacterium (Bn) surrounded the nucleus. Another type (B) was found elsewhere in the cytoplasm. Also in the cytoplasm were the following: food vacuoles enclosing various algae, relatively clear vacuoles and vesicles, glycogen, various electron-opaque particles, and occasional microtubules. The plasmalemma was smooth, lacking the external fringe which characterizes other large fresh-water amoebae.

Notes: SYNOPSIS. Cysts of Sarcocystis sp. are described from a dog. They are spherical to elongate, 110–250 μ in diameter, and contain numerous crescentic trophozoites measuring 4–5 × 1.5 μ. No septa were seen. This is the first report of Sarcocystis from a domestic carnivore.

Notes: SYNOPSIS. Cytoplasmic inclusions appear rapidly in Leishmania enriettii exposed to 37 C. The staining of these droplets with oil red O, their extraction in non-polar solvents, and their fine structure by electron microscopy establish their identity as lipid droplets. Fatty acid profiles of these organisms show alterations concomitant with the development of these inclusions. Oleic acid increases while linolenic acid is depressed in cells exposed to elevated temperature. A greater incorporation of exogenous radioactive stearic acid occurs, with depressed specific activities of linoleic and linolenic acids compared to values obtained with control organisms. The isolated lipids of L. enriettii have temperature-dependent changes consistent with a physical interpretation of events which occur with temperature inactivation. The temperature lability of fatty acid metabolism is discussed in terms of the synthesis and stability of cellular membranes and organelles.

Notes: SYNOPSIS. Total counts of Eimeria vilasi and E. wisconsinensis oocysts in 0.05 g fecal samples from the eastern chipmunk over a 2-year period indicated that the 2 species had respective occurrences of 100% and 11% and an actual abundance ratio of 35 to 1. In the red squirrel similar counts of E. tamiasciuri and E. toddi over a 3-year period indicated occurrences of 98% and 6% and an actual abundance ratio of 26 to 1, respectively. These results parallel a similar dichotomy in percent occurrence of 7 Eimeria in the sciurid genera Cynomys and Marmota.

Notes: SYNOPSIS. By means of precipitation with protamine sulfate, a soluble antigen (PS) was obtained from erythrocytes of horses with acute babesiosis due to Babesia caballi and B. equi. This antigen reacted in gel diffusion tests with sera from horses recovered from acute babesiosis. The PS antigen was found to be muco-protein, susceptible to destruction by trypsin and taka-diastase. Analysis of the antigen by paper electrophoresis revealed 2 components which were not present in similar preparations made from erythrocytes of Babesia-free horses.When the PS antigen was heated in boiling water for 30 minutes, a serologically inactive precipitate was formed; however, the supernate remained serologically active and was termed boiled PS (BPS) antigen. This antigen was polysaccharide in nature; its serologic activity was destroyed by taka-diastase.In gel diffusion tests with sera of recovered horses, the PS antigen formed 2 lines of precipitation which coalesced in a single line formed between these sera and the BPS antigen. Both PS and BPS antigens reacted with sera of horses recovered from acute babesiosis in the gel-diffusion test, but not with sera of dogs and rats recovered from acute infection with Babesia canis and Babesia rodhaini, respectively. The serologic specificity of these antigens suggests that they might have application in the serodiagnosis of inapparent Babesia infections of equine animals.

Notes: SYNOPSIS. Euglena gracilis (bacillaris variety, strain SM-L1, streptomycin-bleached) used the following amino adds (10−3 M) as sole nitrogen source for growth on a defined medium: glycine, alanine, valine, leucine, isoleucine, serine, threonine, and glutamic acid. Aspartic acid was used at 10−2 M. Glutamine and asparagine were used at 10−3 M and were better N sources than their parent dicarboxylic amino acids. Not used as sole N source for growth were phenylalanine, tyrosine, tryptophan, cysteine, cystine, methionine, proline, hydroxyproline, histidine, arginine, lysine, and taurine. Astasia longa (Jahn strain) was more restricted than Euglena and used only asparagine and glutamine as N sources for growth.

Notes: SYNOPSIS. Gigantomonas usually exists in the multinucleate stage. Hence, multiple fission is more common than binary fission. In its flagellate as well as its aflagellate state it is always an amoeboid cell which possesses from one to several large, clear pseudopodia. Fairly often in the multinucleate, as well as the uninucleate, stage no extranuclear organelles are present except large plain centrioles, two of which are always closely associated with each nucleus. During nuclear reproduction four centrioles, two old ones and two new ones, are always present with each nucleus. During all nuclear reproductions, regardless of the number of nuclei present, extranuclear organelles, such as flagella, axostyle, undulating membrane, and costa when present are discarded. If they are renewed, it is by the new centrioles at the same time that the old ones produce new central spindles, two always cooperating in the process. Thus, Gigantomonas, like other genera of the Devescovinidae, the family to which it belongs, never has for each nucleus present more than one set of extranuclear organelles, a characteristic which Devescovinidae and Lophomonadidae have in common. It is the only genus of Devescovinidae without a parabasal body.Owing to the liquidness of the cytoplasm, the central spindle, which becomes very long indeed, often extends beyond the cytoplasm and thus pushes the nucleus fastened to this end of it completely out of the cell. Mainly because of this situation, multinucleate forms with an odd number of nuclei occur often; otherwise the nuclear numbers would be 2, 4, 8, 16, 32, etc., because, no matter how many nuclei are present, they all reproduce simultaneously or nearly so.An unusual situation occurs in which Gigantomonas ingests and digests a small species of Holomastigotoides, while several hundred individuals of the latter become attached to and destroy Gigantomonas.

Notes: SYNOPSIS. A new species of coccidium is described: Eimeria urosauris n. sp., in the gall bladder of the lizard Urosaurus graciosus Hollowell, from the Mojave Desert in California. The oocyst of E. urosauris is smooth, bilaminar, nearly cylindrical, with long borders only slightly convex, ends rounded and very nearly hemispherical. It is usually 32 × 20 μ, and its length/width ratio is 1.6. It contains 4 ellipsoid sporocysts, each 10.5 × 9 μ, for which 1/w is 1.17. Each sporocyst contains 2 tapered bent sporozoites with rounded ends, 11 μ long, 4 μ in diameter at the larger end, and 1.5 μ in diameter at the smaller end. Each sporocyst also contains a central granular sporocyst residuum 3.5 μ in diameter. The oocyst lacks a micropyle and oocyst residuum, and there is no Stieda body on the sporocyst. Sporulation time is 6–10 hr. Endogenous development, with reinfection by liberated sporozoites, occurs in the epithelial lining of the gall bladder. E. urosauris is compared to other morphologically similar lacertilian eimerias with which it might be confused.

Notes: SYNOPSIS. In rats infected with T. lewisi, 2 morphologically distinct forms of the trypanosome occur. By means of the immunodiffusion technic several antigenic differences between the 2 forms were observed. The time course in the antigenic and morphologic changes is somewhat different. The antigenic change from young to adult forms is gradual. It starts 12 days after infection and is complete in 14 days, 3 to 5 days after the morphologic appearance of the trypanosomes is that of adult forms. In addition, there appear to be 2 separate stages of young forms when they are analyzed for antigenic composition.

Notes: SYNOPSIS. Nucleic acid hybridisation involving DNA samples was used to study relationships between various protozoa. The most hybridisation or nucleic acid homology was always in the homologous reaction between 2 DNA samples from the same source. It was concluded that all the protozoa tested have nucleotide sequences or genes in common with Paramecium aurelia. The ciliates could be placed in a sequence of decreasing homology relative to Paramecium: Tetrahymena, Colpidium, Stentor, Didinium, Dileptus, Blepharisma. Actinosphaerium had fewer sequences than any of the ciliates and the flagellate Euglena had the fewest sequences in common. The bacterium Aerobacter had none. Similar relationships were inferred from competitive hybridisation experiments; these relationships were also in general mirrored by morphologic relationships and overall G + C base compositions which ranged from 46% for Euglena to 32% for P. aurelia. These experiments, it is hoped, will contribute to studies on origins of the metazoa.

Notes: SYNOPSIS. Nicotinamide adenine dinucleotide phosphate (NADP) and nicotinamide adenine dinucleotide (NAD) linked isocitrate dehydrogenase and NADP linked alcohol dehydrogenase have been detected in Euglena gracilis var. bacillaris.The NADP isocitrate dehydrogenase showed half-maximal activity at a concentration of 3 × 10−5 M DL-isocitrate, but did not follow simple Michaelis-Menten kinetics with respect to substrate concentration. The optimal NADP concentration was about 0.06 mM, and activity fell off sharply on either side of this optimum. Fresh preparations of the enzyme migrated as single bands in disc electrophoresis, but two enzymatically active bands were present after frozen storage.The NAD isocitrate dehydrogenase followed Michaelis-Menten kinetics with respect to substrate. In crude extracts, no requirement for adenosine monophosphate, adenosine diphosphate, or sulfhydryl compounds could be found.NADP alcohol dehydrogenase activity could be found with either ethanol or propanol as substrate. Low concentrations of coenzyme A were moderately inhibitory.In tris(hydroxymethyl) aminomethane buffer (tris buffer), Euglena extracts reduced NAD slowly in the absence of exogenous substrate. In the absence of tris, no such reduction occurred. A similar phenomenon was observed with NADP.

Notes: SYNOPSIS. Hepatocystis has been found extremely common in a number of species of Formosan mammals, notably the large leafnosed bat (Hipposideros armiger terasensis), the Formosan macaque (Macaca cyclopis), and various subspecies of the red-bellied tree squirrel (Callosciurus erythraeus). Less often infected were the long-winged bat (Miniopterus schreibersii) and the Formosan giant flying squirrel (Petaurista grandis). The species occurring in H. a. terasensis is believed to be new, and is named Hepatocystis hipposideri. It causes considerable enlargement (but not other changes) of the host cell, is often amoeboid, and usually has numerous fine pigment granules.

Notes: SYNOPSIS. Tracer technic has proved to be an excellent tool in the study of predator-prey relationships among the foraminifera. More than fifty axenic species of protists including diatoms, dinoflagellates, chlorophytes, chrysophytes, cyanophytes, bacteria and yeasts were tested as potential food for Allogromia sp (NF), A. laticollaris, Am. monia beccarii, Quinqueloculina spp, Rosalina floridana, Anomalina sp, Elphidium sp, Spiroloculina hyalina, Globigerina bulloides, and Globorotalia truncatulinoides. Although many types of potential food are present in the environment, foraminifera select only certain organisms. The yeasts, cyanophytes, dinoflagellates, chrysophytes and most bacteria tested were not eaten. Selected species of diatoms, chlorophytes and bacteria were eaten in large quantity. Three additional factors affect feeding: the “age” of the food organism, the “age” of the foraminifer or its position in the life cycle, and the concentration of the food. Feeding by foraminifera on most food is erratic below a concentration of 103 organisms and is approximately directly proportional to concentration within a range of 103-106 organisms per 10 ml experimental tube. A natural bloom of Protelphidium tisburyensis was analyzed. A high concentration of 6 species of diatoms characterized the community. A “bloom”-feeder hypothesis for foraminiferal nutrition is presented.

Notes: SYNOPSIS. The reorganization in resting cysts which produce a single emerging individual was followed in 5 species of Colpodidae forming a possible evolutionary series with increasing numbers of kineties. Stomatogenesis in Colpoda maupasi and C. inflata was studied for the first time; that in C. steinii, C. cucullus and Tillina magna was reinvestigated with new observations. In all, the oral primordium is double and originates from segments of certain somatic kineties, constant for each species. The larger mouthparts in the larger ciliates are produced from a correspondingly greater number of kineties. Morphogenetic and evolutionary implications of this series of observations are discussed.

Notes: SYNOPSIS. When large batches of Paramecium (more than 100,000 cells) are centrifuged in conventional centrifuges, extensive lysis occurs, typically lowering recovery to around 30%. An easily constructed centrifuge with a cylindrical plastic head operated at low accelerations permits centrifugation of large batches of Paramecium with about 90% recovery, even after exhaustive washing. Operation requires only a few minutes, and the system is easily cleaned. The inexpensive heads can be instantly interchanged, and cultures can even be centrifuged in their original low form glass culture vessels. This system, which should be applicable to any large fragile cells, permits timed experiments that are usually impossible because of the need for exhaustive washing or concentration from large initial volumes.

Notes: SYNOPSIS. Defined media for Leptomonas collosoma, L. mirabilis, and L. sp. from Dysdercus are described. In addition to factors required by Crithidia spp., including a source of Crithidia factor, all 3 organisms require glycine. Leptomonas collosoma and L. sp. from Dysdercus require choline. All trypanosomatids thus far studied require calcium pantothenate but L. collosoma has an especially large requirement. Leptomonas mirabilis but not L. sp. from Dysdercus can synthesize methionine from homocysteine thiolactone during growth. Homocysteine thiolactone is toxic to L. sp. from Dysdercus. Methionine plus vitamin B12 partly annul homocysteine thiolactone toxicity but only if glycine is also present.

Notes: SYNOPSIS. Glauconema trihymene n. g., n. sp., a marine hymenostome ciliate, is described from the Virginia coast. Morphologic studies were made on specimens treated with the Chatton-Lwoff silver impregnation technic and on animals observed with the phase microscope. Particular attention is given to the buccal ciliature and its importance to generic assignment in the order Hymenostomatida.