ALBERT

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

Notes: SYNOPSIS. A piroplasm occurring in the erythrocytes of 38 of 42 echidnas (Tachyglossus aculeatus) has been described and named Babesia tachyglossi.

Notes: SYNOPSIS. Identical cultural forms of Trypanosoma granulosae occur in NNN agar, Diamonds SNB-9 agar and Proteosepeptone blood agar. The inclusion of penicillin G sulfate and streptomycin had no effect upon the cultures. The first cultural forms to appear (24 hours) were long, slender crithidia which divided to produce short slender crithidia. The latter were the only forms encountered until the 18th day when rosettes, composed of 3–10 short, slender crithidia were found. Following the production of metacyclic trypanosomes (24th day) the culture rapidly died. Transfer of metacyclic trypanosomes and rosettes did not extend the length of culture life. T. diemyctyli is also unaffected by antibiotics and shows similar growth in all media used. Division in this species begins 50–96 hours after inoculation with the production, from the blood stream form, of two unequal, plump crithidia. These divide twice to form slender crithidia; the latter rapidly divide, but do not separate, and yield rosettes with a maximum number of 60 individuals. As the slender crithidia leave the rosette each either remains in the same form or transforms to a plump, pear shaped individual. Secondary rosettes are then formed from the latter. Metacyclic trypanosomes appear, in small numbers, after the 14th day.

Notes: SYNOPSIS. In a survey of coccidia of rodents from Harbel, Libera, the following species of Eimeria were found and described: E. musculoidei n. sp. from Mus (Leggada) musculoides; E. separata Becker & Hall, 1931 from Rattus (Dephomys) defua (new host record); E. praomysis n. sp. from Rattus (Praomys) tullbergi rostratus; E. dasymysis n. sp. from Dasymys incomptus rufulus; E. lemniscomysis n. sp. from Lemniscomys striatus striatus; and E. lophuromysis n. sp., E. sikapusii n. sp., E. liberiensis n. sp., E. harbelensis n. sp., E. africana n. sp., and E. kruidenieri n. sp. from Lophuromys sikapusi sikapusi.

Notes: SYNOPSIS. The morphology of 4 genera of the family Trypanosomatidae has been studied with particular reference to the contractile vacuole, reservoir, flagellum, undulating membrane, kinetoplast, and nucleus. Both the contractile vacuole and reservoir have been found in all species examined. Four morphological types of culture forms are described with special reference to these structures: (1), the Crithidia fasciculata type which is short and membraneless with a rounded posterior end, truncate anterior end and a well developed reservoir; (2) the Herpetomonas muscarum type with no undulating membrane, a truncate posterior end, a rounded anterior end and a reservoir which varies in length from about 1/6 of the length of the body to the full length of the body; (3) the Leishmania type with no undulating membrane, a pointed posterior end, an asymmetrical anterior end and a short reservoir which remains constant in size; and (4), the short-membraned type exemplified by Trypanosoma cruzi, with a pointed posterior end, a short reservoir near the middle of the body and the flagellum attached to the body along a portion of its length. This last form is derived from the blood stream morphology as exemplified by Trypanosoma lewisi in the rat by a shifting of the kinetoplast, flagellum, reservoir and contractile vacuole along the surface of the body from a position posterior to a position anterior to the nucleus.

Notes: SYNOPSIS. Exposure to non-lethal doses of ultraviolet completely inactivates chloroplast development and chlorophyll synthesis in Euglena gracilis var. bacillaris and in the Z strain. Treatment with visible light immediately following UV reverses the inactivation completely. The presence of chloroplasts is not necessary for this inactivation since similar results are obtained with light-grown cells (containing chloroplasts) and dark-grown cells (lacking chloroplasts).

Notes: SYNOPSIS. Strains of Trypanosoma rhodesiense resistant to atoxyl and to antrypol respectively were allowed to multiply in the blood of mice and were also maintained for some hours in the gut of tsetse flies. They failed to acquire cross-resistance as shown by tests with the respective drugs given singly and in combination to infected mice.

Notes: SYNOPSIS. Paramecium multimicronucleatum was grown in a buffered desiccated lettuce medium maintained at pH 7.5, with Aerobacter aerogenes the main bacterial source. The maximum expansion in length and width was at pH 6.0; the minimum expansion in length and width at pH 8.5. The paramecia were usually stouter at pH levels 〈 7.0 except at pH 5.5 and generally more slender 〉 pH 7.0.The pH of the medium affected the size of food vacuoles as indicated by the fact that the maximum food vacuolar diameter was at pH 6.0, the minimum at 7.0.The fastest and greatest expansion of food vacuole diam. was at a relative viscosity of 8; the minimum food vacuolar diam. was in controls (without gum arabic) having a viscosity of 1.3.

Notes: SYNOPSIS. Trypanosoma granulosae n. sp. was found in the salamander, Taricha granulosa twittyi, from Dutch Bill Creek, Sonoma County, California. This polymorphic trypanosome has an anterior nucleus containing a definite endosome. The kinetoplast is rod-shaped and never contained within a vacuole. Myonemes are occasionally seen in slender individuals.

Notes: SYNOPSIS. Balantidium coli was cultured for 4 months in Dobell-Laidlaw's medium. About 10 specimens of monsters were found in the preparations (Chatton-Lwoff silver impregnation technique). One individual showed a tendency to polystomy. One doublet of Balantidium caviae (?) in preparations treated by the same technique was found in a population from a guinea pig.The monsters of Balantidium coli are either single distomic individuals or doublets (homopolar or heteropolar).The infraciliature of the monsters shows different degrees of deviation from the normal pattern. No reorganization field during the formation of additional cytostomes was observed, which agrees with the data on normal stomatogenesis. This process is very similar in both normal specimens and monsters and is characterized by the arrangement of radiating kineties surrounding the anlage of the cytostome and, evidently, by invagination of this area which later forms the peristome. The fate of single monsters and that of homopelar doublets is unknown. The heteropolar monsters are considered non-viable because the arrangement of the kineties in both presumptive daughters contradicts the rule of desmodexy (Chatton-Lwoff).The occurrence of the monsters in cultures may possibly be explained by the action of acriflavine which is mutagenic for Escherichia coli, or by gentian-violet which inhibits fission of sea urchin eggs.This paper apparently constitutes the first presentation of anomalies of the infraciliature in parasitic ciliates.In addition the exact arrangement of the kineties and kinetosomes at the posterior pole of Balantidium coli is described.

Notes: SYNOPSIS. A nonpathogenic strain of Histomonas was used in an attempt to immunize young turkeys against blackhead. Rectal inoculation of several thousand nonpathogenic histomonads on 2 or 3 consecutive days afforded considerable protection against modest rectal challenges with pathogenic histomonads 3 to 6 weeks later, but was much less effective against pathogenic histomonads introduced by feeding eggs of Heterakis gallinae. It is believed that an immune barrier limited to the surface of the cecal mucosa was established, and that the larvae of the cecal worms often penetrated this barrier before liberating their histomonads, thus permitting blackhead to develop. Immunization by the introduction of nonpathogenic histomonads with Heterakis eggs was not satisfactory. Apparently, the nonpathogenic organisms introduced in this way were too few to assure formation of an intact barrier.

Notes: SYNOPSIS. Podophrya collini was fed homozygous killer Paramecium aurelia (containing kappa particles DNA). The rate of giant formation in the suctorian population was then determined; controls were fed homozygous sensitive P. aurelia. No difference in the rate of giant formation was observed; the DNA contribution by the kappa particles was not enough to induce a higher rate of giant formation. Cultures of P. collini containing only animals of known uniform age were then fed controlled numbers of Tetrahymena pyriformis or sensitive P. aurelia after these ciliates had been pretreated with guanylic acid, 8-azaguanine, commercial DNA or DNA isolated from Tetrahymena. Giant formation was increased after guanylic acid pretreatment, reduced after the 8-azaguanine pretreatment, and unaffected after DNA pretreatment over a 5-day test period. The changes in rate of giant formation are clearly caused by pretreatment agents. These agents reach the suctorian's metabolism via the food ciliates' food vacuoles before they are altered in the food vacuole.

Notes: SYNOPSIS. Polytomella caeca utilizes as sole carbon sources in chemically defined media: acetate, propionate, butyrate, valerate, pyruvate, succinate, ethyl, butyl, amyl, and hexyl alcohols. Glyceraldehyde and α-ketoglutarate sustain very small populations. Caproate, caprylate, fumarate, malate, propyl, heptyl, and octyl alcohols and the iso-compounds iso-butyrate, iso-butyl and iso-hexyl alcohols are inadequate.Acetate is not assimilated 〈pH 5.0, propionate and butyrate 〈pH 6.0, and valerate 〈pH 7.0. Optimum for utilization of succinate is pH 3.0, for pyruvate pH 4.0, utilized also at pH 2.0 Fatty acids are utilized dissociated; succinate and pyruvate are utilized undissociated. Alcohols are assimilated throughout pH 4.0–7.4, except hexanol at pH 7.4. Alcohol availability is proportional to molecular length-1.pH after growth of fatty acid media is 8.4 ± 0.4; stable in pH 2.0 pyruvate and pH 3.0 succinate media; 3.5 ± 0.3 in alcohol media with initial pH 〈6.0. Longer alcohols cause less pH decrease during growth.Acetate concentrations 〈0.2% do not support maximum populations; concentrations of 0.2–1.0% do. pH after growth increases in these media to pH 8.5 with maximum populations.Malate, fumarate, α-ketoglutarate, and lactate seem not to penetrate the cell, but are metabolized by homogenates. Methylene blue reduction by homogenates indicates the presence of lactic, malic, succinic and α-ketoglutaric dehydrogenases, fumarase and glutamic transaminase. Extracts contain Embden-Meyerhof phosphate esters, ATP, and ADP.

Notes: SYNOPSIS. An immunity to reinfection with E. bovis was demonstrated in 3 experiments involving 60 calves. This immunity develops rapidly, as indicated by resistance to a challenge given 14 days after the immunizing inoculation. In 3 groups of 3 to 6 young calves each, immunity was still present to a moderate degree 2 to 3 months after inoculation; in one group of 5 animals about a year old there was apparently a high degree of immunity about 7 months after the last inoculation. In one experiment an immunizing inoculum of 10,000 oöcysts did not produce as much immunity as 50,000 oöcysts. In 2 experiments there appeared to be little difference in the immunity produced by a single inoculation of 50,000 as compared with 100,000 oöcysts, but inoculation with 100,000 oöcysts, resulted in substantially longer and more severe illness than 50,000 oöcysts. There appeared to be no appreciable difference in clinical symptoms or development of immunity between calves given a single immunizing inoculum and those given the same number of oöcysts in 5 equal inocula on successive days. Treatment with sulfamethazine and sulfamerazine (Merameth) 13 to 15 days after inoculation alleviated the clinical symptoms of coccidiosis without interfering appreciably with the development of immunity. In one experiment with 7 calves, no beneficial effect was noted from 1 or 2 transfusions of 500 ml. of plasma and leucocytes from immune calves into 4 calves 1 and 12 days or 11 days after a challenge inoculation.

Notes: SYNOPSIS. Experiments were carried out to determine if the course of infection with Plasmodium cathemerium was changed when the temperature of incubation of the duck embryo host was lowered. At 30° C. the infection developed more slowly and never reached the peak seen in infected embryos incubated at 37° C. If infected embryos at 30° were returned to 37° C. the resultant parasitemia developed similarly to that usually seen in this host at the latter temperature. Studies of the periodic behavior of the parasite at 30° C. and 38° C. revealed no differences in the time of segmentation. Merozoite counts were unchanged. The reduced parasitemia in embryos at 30° C. may result from reduced ability of the parasite to penetrate new host cells.

Notes: SYNOPSIS. Traditionally, observations on the nature of protozoa have been published in periodicals or books, or remain buried in research notebooks. The retrieval and processing of information on a particular species or strain are dependent solely upon individual investigators. Although various modern methods have been applied to the study of protozoa, no attempt has been made to develop a system with which information on protozoan strains can be stored, retrieved easily, and processed for various analyses by computer technology. Based upon an existing system for encoding data on bacterial strains, a complementary system applicable to protozoan strains was developed and is described herein.

Notes: SYNOPSIS. The development of Sarcocystis cruzi Hasselmann (syn. S. fusiformis Railliet) meronts was studied in seven 7- to 10-day-old calves killed 4, 7, 11, 15, 22, 25 and 28 days postinoculation (DPI) with 5 × 107 sporocysts from feces of coyotes. No meronts were found 4 and 7 DPI. Young and intermediate meronts with 1–16 nuclei were found in endothelial cells of arteries in mesenteric lymph nodes, but not in kidneys 11 DPI.Mature meronts were noted in endothelial cells of arteries, arterioles, or capillaries of many organs of calves killed 15 to 25 DPI. No first-generation meronts were found 28 DPI. By electron microscopy, all stages of the first-generation merogony were found free within the host cell cytoplasm and not within a parasitophorous vacuole. The appearance of intranuclear spindles preceded the formation of merozoites by endopolygeny. Mature meronts measured 41.0 × 17.5 (34–50 × 15–24) μm, contained ∼ 100–350 merozoites, and had 2 to 4 relatively small residual bodies, 2.8 μm in diameter. Merozoites measured 6.3 × 1.5 (5.5–7 × 1 μm) and contained most of the organelles characteristically found in coccidian merozoites. Micropores were observed in merozoites, but not in young and intermediate meronts. Merozoites were seen free in the lumen of blood vessels, in intracellular areas, and free within the host cell cytoplasm.

Notes: SYNOPSIS. Myxidium spores from various eel hosts (Anguilla spp.) are compared. Myxidium anguillae, M. enchelypterygii, M. illinoisense, M. serum, and M. zealandicum are synonymized with M. giardi, a ubiquitous species reported from A. anguilla, A. rostrata, A. mossambica, A. japonica, A. reinhardtii, A. bicolor pacifica, A. australis, and A. dieffenbachii. Myxidium uchiyamae, M. lentiforme, M. matsuii and M. acinum are retained, and 2 new species described. Species other than M. giardi appear to be restricted to the Indo-Pacific region.

Notes: SYNOPSIS. A new species of kinetophragminophoran ciliate, collected from dried vegetation and capable of forming an aerial sorocarp, is described and named Sorogena stoianovitchae gen. n., sp. n. This ciliate is a voracious predator that feeds on species of Colpoda, and, when the latter is depleted in numbers, aggregates to forms sorogens. Each sorogen rises into the air from the surface of the water, forming a secreted stalk with a sorus of cysts at its apex. the feeding stage of the ciliate resembles an Enchelys in that it has an apical, slit-like mouth surrounded by a lip, a somewhat dorso-ventrally flattened body, and meridional kineties. Its length ranges from 40–75 μm and width from 23–55 μm. It has a typical rhabdos type of cytopharynx, but no specialized oral ciliature. the somatic kineties are formed of rows of paired kinetosomes with associated microfibrils, the arrangement of which differs a little from that of other ciliates of this subclass. Sorogena has tentatively been placed in the order Haptorida although it lacks toxicysts, recognizable mucocysts, and clavate cilia. Its unique life cycle and some of the details of its fine structure indicate differences between Sorogena and other haptorids so profound that a new family, SOROGENIDAE, is created for it. the type species (PNG76-73) was collected on dry figs at the Wau Ecology Institute, Papua New Guinea.

Notes: Cell surface pellicular membranes (PM) were isolated from promastigote forms of Leishmania donovani by differential and discontinuous sucrose gradient centrifugation procedures. the PM had a density equivalent of ∼ 1.19 g/cm3. As ascertained by electron microscopy, longitudinal parallel arrays of subpellicular microtubules (MT) remained attached to the isolated PM inner lamina, and this feature was used to assess membrane fraction purity. Gradient fractions having ∼ 95% of all membranes combined with MT were obtained routinely. the attached MT imparted a structural asymmetry to the PM permitting uniequivocal identification of the membrane external and cytoplasmic surfaces. the supramolecular structure of attached MT was evident in negatively stained PM. In ultrathin sections, PM had a mean width of ∼ 7.2 nm and attached MT a diameter of ∼ 29 nm. the MT were apparently cross-bridged both to each other and to the PM via a flocculent filamentoid nexus. As determined by sodium dodecylsulfate-polyacrylamide gel electrophoresis, isolated PM contained ∼ 40 peptide bands ranging in apparent molecular weight from ≤ 1.2 × 104 to ≥ 2.2 × 105daltons. of these, 19 were stained with periodic acid-Schiffs’ reagent suggesting that most PM carbohydrate constituents were present as glycopeptides. A presumpative glycolipid/polysaccharide PM constituent was also identified in such gels.

Notes: Organic requirements for attachment to glass, elongation, and motility of Entamoeba histolytica, have been determined. the trophozoite, which has been grown axenically only in highly complex media with reduced oxygen tensions, remains rounded and detached when placed in a Tris-HCl buffered solution containing NaCI, KCI, MgCI2, and CaCI2. A maintenance medium in which the amebae could attach to glass, elongate, and remain motile and viable for 12 to 24 h was devised with the addition of cysteine, ascorbic acid, bovine serum albumin, and the vitamin solution of medium NCTC #107. Tris-HCI was the most effective buffer tested and the optimal pH was 6.9 to 7.0. Survival, but not attachment, of the amebae was decreased at osmolalities ranging between 110 and 180 milliosmoles/kg, whereas both functions were decreased above ∼260 milliosmoles/kg. Bovine serum albumin, the most effective of the proteins tested, and the vitamin solution helped maintain attachment of some ameba strains, but were not required by other strains. the requirements for cysteine and ascorbic acid were absolute and highly specific. During incubation in the maintenance medium, cell volumes decreased. Sensitivity of the organisms to agglutination by concanavalin A, wheat germ agglutinin, soybean agglutinin and fucose binding protein remained unchanged.