ALBERT

Notes: The paper describes two research projects on the application and value of satellite imagery taken, by ERTS 1 and Skylab, for small scale mapping. It describes the methods used in controlling a block of normal system corrected imagery and the accuracies achieved.The interpretation and evaluation of the imagery are discussed and the results of ERTS 1 and Skylab in this field are compared. Finally, some examples are described where ERTS 1 imagery has proved of practical value as a navigational aid when flying conventional photography and airborne geophysical surveys and for providing base maps when concerned with resource evaluation of poorly mapped areas.〈section xml:id="abs1-2"〉〈title type="main"〉Résumé On présent les résultats de deux projets de recherche sur les applications possibles el la valeur pratique des imageries satellitaires, prises avec ERTS 1 et Skylab en vue de la cartographie à petite échelle. On décrit les méthodes utilisées pour “appuyer” un bloc à imagerie corrigée (système normal) et l'exactitude obtenue. On compare de ce point de vue ERTS 1 et Skylab. Enfin on donne quelques applications pratiques qui se sont révélées utiles: aide à la navigation pour les levés photographiques et géophysiques aériens; établissement de cartes expédiées en vue d'inventaire de régions souscartographiées.〈section xml:id="abs1-3"〉〈title type="main"〉Zusammenfassung Beschreibung von zwei Forschungsprojekten über die Anwendung und den Nutzen von Satelliten-Bildern, die von ERTS 1 und Skylab aus aufgenommen wurden, für die Herstellung kleinmassstäbiger Karten. Es werden die Verfahren beschrieben, die beim Festpunktanschluss von korrigierten Bildern angewendet wurden. Die dabei erreichten Genauigkeiten werden mitgeteilt. Diskussion der Interpretation und Bewertung der Bilder und Vergleich der diesbezüglichen Ergebnisse von ERTS 1 und Skylab. Schliesslich werden einige Beispiele beschrieben, wo Bilder von ERTS 1 von praktischem Wert als Navigationshilfe zur Luftbildaufnahme und geophysikalischen Lufterkundung und bei Beschaffung von Grundkarten bei der Ressourcenerkundung in kartographisch schwach erfassten Gebieten waren.

Notes: The author reviews the present state of aerial triangulation methods and outlines the requirements for future research which were suggested at the symposium of Commission III of the International Society for Photogrammetry in 1974. He maintains that none of these research topics is very relevant to aerial triangulation as it is practised in Britain today. A combination of complacency, the natural inertia imposed by economic arguments and the higher priorities accorded to younger developments such as automated cartography is conspiring to prevent replacement of adequate but out-dated methods. He considers that there are nevertheless, strong arguments for selecting a newly designed, optimum, modern system, based on a modular approach, which can be introduced on a national basis and made fully available to all interested organisations.〈section xml:id="abs1-2"〉〈title type="main"〉RésuméRevue de l'état actuel des méthodes de triangulation aérienne et rappel des voies de recherches recommandées au symposium de la Commission III de la SIP en 1974. Aucune de ces voies n'a malheureusement de rapport avec ce qui est actuellement pratiqué en Grande Bretagne en matière de triangulation aérienne. Une certaine complaisance, mêlée à une inertie assez naturelle due à des raisons économiques et à la plus grande priorité accordée à des domaines plus neufs comme la cartographie automatique, a perpétué l'emploi des méthodes pertinentes mais désuètes. L'auteur pense qu'il y a de puissants arguments pour qu'on choisisse et mette en oeuvre une méthode moderne, avec approche modulaire dont l'emploi se ferait à l'échelle nationale et à laquelle tout organisme intéressé pourrait recourir.〈section xml:id="abs1-3"〉〈title type="main"〉ZusammenfassungDer Autor referiert über den gegenwärtigen Stand der Verfahren der Aerotriangulation und skizziert die Anforderungen für künftige Forschungs-arbeiten, die auf dem Symposium der Kommission III der Internationalen Gesellschaft für Photogrammetrie 1974 vorgeschlagen wurden. Er bekräftigt, dass keiner dieser Forschungsgegenstände bezüglich der gegenwärtig in Grossbritannien praktizierten Aerotriangulation relevant ist. Eine Kombination von Selbstzufriedenheit, natürlicher Beschränkung infolge ökonomischer Argumente und der höheren Prioritäten wegen der neueren Entwicklungen z.B. in der automatischen Kartographie verhindert den Ersatz passender, aber unmoderner Verfahren. Der Autor ist der Meinung, dass es trotzdem starke Argumente zur Auswahl eines neuen optimalen, modernen Systems gibt, das auf dem Bausteinprinzip beruht und das auf nationaler Grundlage eingeführt und allen interessierten Organisationen zugänglich gemacht werden kann.

Notes: A plot of relative parallax measurements in a student exercise is proposed for revealing errors in parallax bar readings taken from a stereo-pair of aerial photographs. The sensitivity of the computed heights to measurement error is also evaluated.〈section xml:id="abs1-2"〉〈title type="main"〉RésuméOn propose un tracé graphique des mesures de parallaxe pour mettre en évidence des erreurs de lecture à la barre de parallaxe.〈section xml:id="abs1-3"〉〈title type="main"〉ZusammenfassungEs wird eine Auswertung relativer Parallaxenmessungen bei einer studentischen Übung vorgeschlagen, um Fehler der an einem Stereomikrometer vorgenommenen Ablesungen aufzudecken, die an Hand eines Luftbildpaars erfolgten. Der Einfluss des Messfehiers auf den Höhenfehler wird ebenfalls abgeschätzt.

Notes: 1:70 000 scale photographs taken over Syria with a Russian AFA topographic camera equipped with a Russar 29b super-wide angle lens have been tested. The tests included (i) the measurement of a field of points using several different instruments and a comparison of the photogrammetrically derived co-ordinates with the values derived by field survey; (ii) the production of plots at 1: 25 000 scale for comparison with a check plot produced from large scale, wide angle photography; and (iii) production of orthophotographs, also at 1: 25 000 scale. Difficulties were experienced with the asymmetrical lens distortion pattern and the variations in illumination and resolution present in the photography. The former were overcome by manufacture of asymmetrical lens distortion correction plates. When this was done, the accuracies attained were comparable to those achieved in previous tests using photographs taken at the same scale with the Wild RC 9 camera equipped with the Super Aviogon I lens and measured on the same or similar types of measuring equipment.〈section xml:id="abs1-2"〉〈title type="main"〉Résumé On décrit ici un test relatif à une couverture aérienne au 1: 70 000 exécutée en Syrie avec une chambre russe AFA dotée d'un super-grand angulaire 29 b. Le test comprenait: la détermination d'un polygone au sol, et la comparaison des determinations géodésiques et des déterminations photogrammétriques; la restitution de parcelles au 1: 25 000 en vue de les comparer avec une parcelle-test provenant de photos à grande échelle; et la réalisation d'ortho-photos au 1: 25 000. La distorsion disymétrique de l'objectif a conduit à quelques difficultés, ainsi que des inégalités d'éclairement et de finesse sur les clichés. On a surmonté les premières en faisant fabriquer des plaques correctives. Ceci fait, l'exactitude atteinte s'est trouvée du même ordre que celle de restitutions provenant des clichés aux même échelles pris avec le Wild RC9 et effectuées dans des conditions très voisines.〈section xml:id="abs1-3"〉〈title type="main"〉Zusammenfassung Bericht über die Testung von Luftbildern (mb= 70 000), die über Syrien mit einer sowjetischen Überweitwinkelkammer mil einem Russar-Objektiv 29b aufgenommen wurden. Die Untersuchungen umfassten (a) die Aus-messung eines Punktfeldes mit verschiedenen Auswertegeräten und einen Vergleich photogrammetrisch und geodätisch bestimmter Koordinaten, (b) die Durchführung einer Auswertung 1: 25 000 und den Vergleich mit einer aus grossmassstäbigen Weitwinkelbildern abgeleiteten Kontrollkarte, (c) die Herstellung von Orthophotos im Massstab 1: 25 000. Schwierig-keiten resultierten aus der asymmetrischen Objektivverzeichnung und den Variationen in der Bildhelligkeit und -auflösung. Die Verzeichnung konnte durch Herstellung von Kompensationsplatten reduziert werden. Danach waren die erreichten Genauigkeiten mit den in früheren Tests erzielten vergleichbar, bei denen mit einer Wild RC9- Kammer (Super Aviogon I) aufgenommene Luftbilder gleichen Massstabs an denselben oder ühnlichen Auswertegeräten ausgemessen wurden.

Notes: With present day trends towards smaller scale photography for topographic mapping and photomapping, there is an increasing need for high quality photography and a corresponding need for diagnostic information on potential sources of degradation. Hence subjective judgements must be supplemented by quantitative analyses of image quality that go beyond mere determinations of resolution level. A methodology for evaluating three important parameters governing image quality (development, exposure and spatial frequency content) is presented. By sequentially comparing the values measured on production or test photographs with standard values, the faults most commonly responsible for image degradation (such as errors in development and exposure, excessive image motion, vacuum failure and poor camera focus) can be isolated and measured.〈section xml:id="abs1-2"〉〈title type="main"〉RésuméLa tendance actuelle en matière de plans topographiques et de photocartes est de diminuer l'échelle de la couverture photo; se fait done jour le besoin d'émulsions de haute qualité et simultanément la nécessité de pouvoir juger objectivement de cette qualité. II faut alors recourir á des analyses quantitatives qui aillent au-delá de la simple mesure du pouvoir de résolution. On présente ici une méthodologie relative au problème de l'évaluation de trois des principaux paramètres effectuant la qualité de l'image (développement, durée d'exposition, résolution de fréquence spatiale). Avec des tests d'homogénéïté on peut alors déceler les variations de qualité, et en particulier déterminer et mesurer les causes d'altération les plus fréquentes (erreurs lors du développement ou lors de la phase d'exposition, filé, défauts internes, qualité médiocre de la chambre).〈section xml:id="abs1-3"〉〈title type="main"〉ZusammenfassungBei dem gegenwärtigen Trend, den Bildmassstab zur Herstellung von topographischen Karten und Photokarten zu verkleinern, ergibt sich zunehmend die Notwendigkeit, Hochleistungsphotos aufzunehmen und diagnostische Informationen über mögliche Quellen der Qualitätsverschlechterung zu erlangen. Insbesondere müssen subjektive Bewertungen durch quantitative Analysen der Bildqualität ergänzt werden, die über Bestimmungen des Auflösungsvermögens hinausgehen. Es wird eine Methodologie zur Bewertung von drei wichtigen Parametern (Entwicklung, Belichtung, Inhalt der Orts-frequenz), die die Bildqualität beeinflussen, angegeben. Durch Vergleich der auf Produktionsbildern oder Testbildern gemessenen Werte mit deren Standards können die Fehler, die meistens eine Bildverschlechterung verursachen (wie zum Beispiel Fehler bei der Entwicklung und Belichtung, unzulässige Bildwanderung, ungenügende Planlage oder Kammerabstimmung) aufgedeckt und gemessen werden.

Notes: Le microscope électronique à balayage donne l'image de la surface d'un objet situé dans une boîte à spécimen où a été fait le vide. Un fin pinceau d'électrons balaie la surface synchroniquement avec un tube cathodique dont l'intensité est modulée en fonction du signal secondaire émanant du spécimen. Le système présente une grande profondeur de champ; on peut donc obtenir différentes perspectives du spécimen en le photographiant sous diverses inclinaisons (perspectives qui sont centrales, mais cependant justiciables d'être traitées comme parallèles pour de forts grandissements) et donc le restituer spatialement. On donne dans la première partie les limitations pratiques de l'appareillage, ainsi que le type et les causes de distorsion de l'image. Dans la deuxième partie, on décrit les caractéristiques d'un appareil de restitution adaptéà un cas standard: grandissement des deux clichés d'un stéréogramme: fixe-angle d'ouverture du faisceau perspectif négligeable (c'est le cas pour de forte grossissements) et convergence relative des deux positions de la plaque porte-spécimen est fixe.〈section xml:id="abs1-2"〉〈title type="main"〉Zusammenfassung Das Abtast-Elektronen-Mikroskop liefert Bilder der Oberfläche von Objekten, die sich in einer Vakuum-Kammer befinden. Ein feiner Elektronenstrahl tastet die Oberfläche in Synchronisation mit einer Kathodenstrahlröhre ab, deren Lichtpunkthelligkeit von dem sekundären Elektronensignal, das von der Probe ausgeht, moduliert wird. Das System gestattet eine grosse Schärfentiefe und erlaubt dadurch verschiedene Projektionen des zu photo-graphierenden Musters durch Neigung desselben zwischen aufeinanderfolgenden Aufnahmen. Aus der Kenntnis der Geometrie der Projektion (die eine Zentralprojektion ist, jedoch für sehr stark vergrösserte Bilder annähernd als Parallel- oder Orthogonalfall behandelt werden kann) ist es daher möglich, zu dreidimensionalen Analysen durch Messung von Parallaxen zu kommen. Teil I der Arbeit handelt von den praktischen Problemen, die sowohl aus den Grenzen für die mechanische Konstruktion von Muster-Halterungen und Auswertegeräten als auch den Verzerrungen der Bilder resultieren. Teil II beschäftigt sich mit praktischen Gesichtspunkten der bewährten Auswerteinstrumente, die speziell für die Lösung eines standard-isierten Problems der Elektronenmikroskopie konstruiert wurden. Bei diesen wird die Vergrösserung der beiden Halbbilder eines Stereobildpaars konstant gehalten, der Divergenzwinkel der peripheren “Strahlen”, die sich aus dem zentralen “Strahl” ergeben, wird als vernachlässigbar angesehen (was bei Bildern mit starker Vergrösserung der Fall ist) und die Neigungswinkeldifferenz zwischen den zwei Lagen der Probe ist konstant.

Notes: The article describes an experiment in which a production block of aerial triangulation, observed by the method of independent models, was repeatedly computed using differing amounts and configurations of control. The block was recomputed to investigate the effects of control errors, of dispensing with the tie strips and of applying different weights to control and tie points. The connexion between the quality of the join of individual models and that of the adjusted block was also investigated.〈section xml:id="abs1-2"〉〈title type="main"〉RésuméOn décrit une série d'essais effectués sur un bloc de production de triangulation aérienne analytique traité par la méthode des modèles indépendants, destinés àétudier l'influence du nombre et de la configuration des points du canevas d'appui, l'effet d'erreurs sur les points d'appui, l'effet des bandes transversales, et du choix des poids pour les points d'appui et de liaison. On a aussi examiné la corrélation entre la qualityé de l'enchaînement des modèles individuels et celle du bloc compensé.〈section xml:id="abs1-3"〉〈title type="main"〉ZusammenfassungBeschreibung eines Versuchs, bei dem ein Aerotriangulationsblock aus der Produktion, der nach der Methode der unabhängigen Bildpaare beobachtet worden war, wiederholt bei verschiedenen Anzahlen und Anordnungen von Passpunkten berechnet wurde. Die Berechnungen erfolgten zur Abschätzung der Einflüsse von Passpunktfehlern. Weiter wurde der Anschluss zu Nachbarstreifen und die Anwendung verschiedener Gewichte für Pass- und Verbindungspunkte untersucht. Desgleichen wurde der Zusammenhang zwischen der Qualität des Zusammenschlusses einzelner Modelle und der des ausgeglichenen Blockes untersucht.

Notes: SYNOPSIS. When two strains cf T. pyriformis that do not require exogenous pyridoxine are crossed, all progeny grow without the vitamin. Offspring from crosses of two pyridoxine requiring clones require pyridoxine with the exception of a few which will grow without pyridoxine. The ratio is approximately 3:1 favoring the pyridoxine requiring category. In matings involving the homozygous dominant pyridoxine requiring clones with the double recessive mutant, that is +/+ X p/p, all of the resulting progeny need pyridoxine. Test crossing these heterozygotes (+/p) with the parental pyridoxine non-requiring clones (p/p) gives offspring approximating a 1:1 ratio. Matings between two heterozygotes derived from breeding experiments also yield progeny in approximately 3 pyridoxine requiring: 1 pyridoxine non-requiring. All data indicate selection for the heterozygote in the population and a possible selection against either homozygote. The great abundance of heterozygotes and rarity of recessive homozygotes in natural habitats corroborates these findings. The genetic evidence supports a single gene hypothesis although the possibility of multiple closely linked genes cannot be ignored. There is also the possibility that a dominant suppressor gene may function in blocking the activity of the pyridoxine mutant genes. Moreover, if this gene exists it may be incompletely dominant since the heterozygote grows slightly on deficient media.

Notes: SYNOPSIS. Trichodina urinicola was found in newts, Triturus cristatus and T. taeniatus, in three localities in Czechoslovakia. The ciliate populations showed important differences on the basis of which they were separated as three new forms of this species: T. urinicola f. typica, T. urinicola f. bohemica, both from Triturus cristatus, and T. urinicola f. taeniatus from Triturus taeniatus. The great variability of trichodinids is evident from the literature as well as from our own observations, so that these new forms are to be regarded as provisional ones until it is possible to decide on the basis of a large number of observations the extent of specificity and variation of individual endozoic species of Trichodina. A detailed description of these forms is given as well as a comparison with the known species of trichodinids inhabiting the urinary tract of amphibians. A brief comment on the present taxonomy of the Urceolaridae in general is outlined.The need for a uniform description of these ciliates is emphasized; in connection with this, the taxonomic value of individual body characters is discussed. Special attention is paid to the adhesive disk of Trichodina, the structure of which is of greatest importance in the taxonomy of this group. On the basis of Dogel's and Fauré-Fremiet's descriptive methods employed in study of trichodinids, a proposal of a uniform description of Trichodina is made which involves all the important features of these protozoa.

Notes: SYNOPSIS. Several substrains of Euglena gracilis var. bacillaris made chlorotic by treatment with pyribenzamine or streptomycin, or by growth at high temperature (35–36°C.), have been examined for their carotenoid content. They differ from the normal green strain both qualitatively and quantitatively. Some strains produce no detectable carotenoids while the carotenoid concentration in the strains producing most is at best only one-fifth that of the normal strain. In all substrains producing carotenoids, the carotene fraction consists of β-carotene accompanied by some members of the phytofluene series. In only two of these substrains, HB-G and PBZ-G3, are xanthophylls produced in significant amounts. In HB-G, the main pigment is echinenone, and in PBZ-G3 it is zeaxanthin. The significance of these findings is briefly discussed.

Notes: SYNOPSIS. Association of gamonts of Pyxinia crystalligera takes place in the midgut of its beetle host, Dermestes vulpinus. At 25°C. the development of gametocysts to the point of liberation of sporocysts is completed between about 15 hours and 27 hours after the gametocysts are deposited with fecal material. Dehiscence is favored by relative humidities of 0% to 90%, but is not favored by a relative humidity of 100%. During the early development of the gametocysts outside the host, the crystals and paraglycogen granules in the cytoplasm of the associated gamonts become concentrated in large masses. The gametes are formed at the periphery of the gamonts. After fusion of the gametes takes place and the sporoblasts begin to develop, the residual cytoplasm containing the inclusions moves outward to form a continuous layer next to the gametocyst envelope, so that the sporoblasts become crowded into a central core. A few hours before dehiscence is initiated a clear area appears on the upper side of the gametocyst. The contents of the gametocyst begin to shrink away from the envelope except in the region of the clear area. Eventually the sporocysts emerge through the clear area and press against the envelope of the gametocyst, causing formation of a conical papilla in the envelope. With continued pressure from the sporocysts, the papilla ruptures at its tip, and the sporocysts emerge in a continuous thread until dehiscence is completed. The thread of sporocysts may attain a length of about 11 mm.

Notes: SYNOPSIS. The steps leading to purine ring closure were examined in Strigomonas oncopelti. The flagellate has an obligate adenine requirement (hypoxanthine and guanine are inert) when grown without p-aminobenzoic acid. The imidazole counterpart of adenine but not the imidazole counterpart of hypoxanthine was active. A pathway for purine biosynthesis compatible with these results is sketched.

Notes: SYNOPSIS. The Nuttallia of the gerbil is transmitted by Rhipicephalus secundus only if the infected meal is taken by the larva, and the subsequent nymphal stage is the only one which is able to infect. There is no transovarial transmission.Infective trophozoites remain in the larval caeca for about 12 hours after gorging. The infective nymph is able to give rise to new infections at various times after it has been allowed to feed, but never later than the third day after disengagement from the host.

Notes: SYNOPSIS. The process of autogamy in unassociated individuals of Paramecium polycaryum was reported by the author in 1954. In May, 1955, conjugation was first seen in this species in cultures collected by me at Annamalainagar, South India, thus removing it from the list of non-conjugating species. This appears to be the first instance in which the process of autogamy was detected prior to observation of conjugation in the same species. Autogamy occurs in singles of the Indian race and appears to be similar, cytologically, to that of American races. The details of the micronuclear behavior in conjugation parallel those of autogamy in singles. In fact, the conjugation process seems to be one of double autogamy (cytogamy), rather than of reciprocal gametic interchange. Paroral cones, often of fair size, are formed but breakdown of the cones to permit micronuclear passage has not been observed. In conjugation there are the usual three pregamic divisions; the first shows four characteristic crescents. The resulting nuclei may all participate in the second division. Fertilization occurs in the paroral cone area. Frequently, separation of the conjugants takes place immediately after the first division of the synkaryon. The old macronucleus undergoes very little change prior to the last postzygotic micronuclear division in the ex-conjugant, when it goes into a skein condition. Four macronuclear and four micronuclear anlagen are formed in the ex-conjugants at the completion of reorganization. On occasion giant individuals of P. polycaryum were observed to have ingested numbers of Tetrahymena pyriformis. The presence of an unidentified rod-like organism in the cytoplasm of the paramecia (non-conjugating) was detected in one collection from Bangalore, India.

Notes: SYNOPSIS. Fine structure and development of Encephalitozoon cuniculi from rabbits were studied in rabbit choroid plexus (CP) cell cultures and were compared to hamster and mouse microsporida.Sporoplasms had a single limiting membrane and contained a large nucleus. Proliferative forms (schizonts) had double outer membranes, the outermost being associated with the formation of the limiting membrane of vacuoles formed within the host cell cytoplasm. These organisms were often binucleate and divided to form sporonts. Sporonts divided once to form 2 sporoblasts which developed into electron-dense spores. Spores had a thick, 3-layered wall and contained a polar filament.The developmental cycle of E. cuniculi in rabbit CP cultures progressed rapidly. Sporoplasms were observed in host cells at 3 hr postinoculation (PI). By 24 hr PI proliferative forms were associated with host cell cytoplasmic vacuoles which contained developing organisms. Mature spores were present in vacuoles by 2 days PI, indicating that the life cycle in the CP system is ∼ 48 hr.The fine structure and the sequential developmental cycle of the mouse and hamster isolates were observed to be identical to those of the rabbit isolate and different from those of the genus Nosema. It is proposed, therefore, that the 3 organisms represent the same species, Encephalitozoon cuniculi.

Notes: RESUME. Deux espèces d'Enteromonas sont observées, provenant, l'une de l'intestin de Triton, l'autre des crottes du Lapin domestique. La cellule piriforme porte un noyau antérieur et 4 flagelles insérts près du pôle ventral du noyau. Le flagelle récurrent (R) est logé dans une dépression ventrale ou cytostome. Les cinétosomes, disposés en une paire antérieure (#1, #2) et une paire postérieure (#3, R), sont liés entre eux par des microfibrilles. Une fibre microtubulaire située au-dessus du noyau est reliée au cinétosome #1. Une autre fibre microtubulaire sous-nucléaire est homologue de la fibre microtubulaire croisée qui existe chez les cellules de Diplozoaires. Le cytostome est bordé par 2 lèvres: la gauche proéminente et armée par plusieurs rangées de microtubules, la droite contenant seulement une mince fibre microtubulaire associée à des microfibrilles. Le cytostome occupe les 2/3 de la face ventrale. Le flagelle récurrent pénètre dans le cytostome puis dépasse l'extrémite de la cellule. Les Bactéries sont phagocytées au fond du cytostome, entre les 2 lèvres distendues. Elles sont digérées dans les nombreuses vacuoles et les corps résiduels sont évacués par rupture de la membrane cellulaire. L'ergastoplasme est concentré près de la périphérie de la cellule. Il n'y a pas de mitochondrie ni d'appareil de Golgi. Dans les kystes observés la cellule plurinucléée est enfermée dans une enveloppe kystique microfibrillaire, les axonèmes sont libres dans le cytoplasme.Les formes diplomonades sont nombreuses et ressemblent aux cellules d'Hexamita, excepté par le cytostome qui est différent. Dans ces formes, les 2 monades sont souvent disposées selon une symétrie axiale binaire mais quelquefois elles sont associées de façon plus anarchique. La cinétide d'Enteromonas est organisée comme celle d'un zoïde de Diplozoaire. Il est possible que le genre Enteromonas soit à l'origine des Diplomonadida et que l'état diplomonadien transitoire chez Enteromonas se soit stabilisé ensuite chez les Diplomonadida. Enteromonas apparaît plus primitif que les autres genres de Diplomonadida aussi nous proposons de créer 2 sous-ordres: celui des Enteromonadina avec le genre Enteromonas et celui des Diplomonadina avec les genres Trepomonas, Trigonomonas, Hexamita, Spironucleus, Octomitus, Giardia. La disposition des cinétosomes et l'existence du cytostome sont les principaux caractères communs entre Enteromonas et les Retortamonadida, cependant les fibres annexes ne sont pas homologues. Une étude plus complète de la division nucléaire et cellulaire de ces 2 ordres de Zooflagellés est nécessaire pour donner un meilleur schéma évolutif.SYNOPSIS. Fine structure of 2 species of Enteromonas, one from the intestine of the salamander, Triturus vulgaris, and another from the feces of domestic rabbit, Oryctolagus cuniculi, is described. The pyriform cell has an anteriorly located nucleus. The 4 flagella originate from an area near the anterior end of the nucleus. The recurrent flagellum (R) is lodged in a ventral depression or cytostome. The kinetosomes, arranged into 2 pairs, anterior (#1, #2) and posterior (#3, R), are interconnected by microfibrils. One microtubular fiber, connected to kinetosome #1, is situated near the anterior surface of the nucleus. Another, subnuclear, microtubular fiber is homologous to the “crossed'’fiber found in Diplozoa. The cytostome is bordered by 2 lips: the preeminent left lip is equipped with several rows of microtubules, while the right lip contains only a thin microtubular fiber associated with microfibrils. The cytostome occupies 2/3 of the ventral surface. The recurrent flagellum passes over the anterior surface of the cell and then comes to lie in the cytostome. The bacteria are phagocytosed in the bottom part of the cytostome between the 2 distended lips. They are digested in numerous vacuoles. The undigested residual bodies are evacuated by a rupture of the cell membrane. The ergastoplasm is concentrated near the cell periphery. Mitochondria and the Golgi apparatus are absent. In the cyst stage, the multinucleate cell is enclosed in a microfibrillar membrane; the axonemes lie free in the cytoplasm.Diplomonad forms of Enteromonas resembling Hexamita are numerous, except that the cytostome is different in these 2 genera. In such forms, the arrangement of the 2 individuals often has binary axial symmetry, but on occasion they are associated in a more anarchic fashion. The mastigont of Enteromonas is organized like that of a single zooid of a diplozoon. It is possible that the genus Enteromonas is ancestral to Diplomonadida and that the diplomonad state, transitory in Enteromonas, became permanently established in Diplomonadida. Enteromonas appears to be more primitive than the other genera of Diplomonadida. Thus we propose 2 suborders: Enteromonadina, subord. nov. with the genus Enteromonas, and Diplomonadina Wenyon, emend., with the genera Trepomonas, Trigonomonas, Hexamita, Spironucleus, Octomitus, Giardia. The arrangement of the kinetosomes and the existence of a cytostome are the principal characters common to Enteromonas and Retortamonadida, while their “accessory'’fibers are not homologous. A more complete study of division of the 2 zooflagellate orders is necessary for the presentation of a more detailed evolutionary scheme of these groups.

Notes: SYNOPSIS. The effects of some environmental influences on the cycle of Trypanosoma diemyctyli in Triturus v. viridescens are described. Bleeding of the host produced a reduction in the number of trypanosomes but did not affect their growth rate. The temperature at which the host was maintained affected the cycle of the trypanosomes. The length of the post-inoculation latent stage increased from 24 hours at 25°C. to an indefinitely long time at 5°C. The trypanosomes were found to be dimorphic. Adult parasites of the short form had a range of 45–75 μ and those of the long form of 76–116 μ. Growth rate of the trypanosomes was inhibited or greatly retarded at temperatures of 10°C. or lower and was greatest at 25°C. The size attained by the parasites and the number of parasites were greatest at 15°C. At this temperature the infection was pathogenic and the dimorphic parasites were in their long form. At the higher temperatures (20–25°C.) the infection was non-pathogenic with the trypanosomes in their short form.The infection is primarily one of adult newts. Experiments indicated that the larvae were resistant to the trypanosomes at all temperatures while the red efts were not. The latter are usually free from the trypanosomes because they are not exposed to them. Attempts to infect other newts and to locate any cryptic stages by the injection of blood and tissues from infected newts gave negative results.Starvation, sodium salicylate, and treatments used to control fungus infection of the newts had no detectable effects on the trypanosomes.

Notes: SYNOPSIS. A comparative study of five species of Tetrahymena, including thirteen strains, was made to ascertain their ability to act as facultative parasites. A variety of experimental hosts, including both vertebrates and invertebrates, were inoculated with axenic cultures of protozoa. Infections were numerous in both larval and adult insects. Tissues of living vertebrates were invaded by one species of Tetrahymena through artificially produced wounds.

Notes: SYNOPSIS. Unabsorbed, complement-inactivated antisera produced in rabbits were used in an immobilization system to study the serology of 31 strains of Tetrahymena pyriformis grown in axenic cultures at 26°C. Fourteen serological “groups” were found: 1. “H”: H, E, S, GC, L3, W, T, GHH, G1-R and sublines W-P and T-P; 2. “PR”: PR; 3. “GL”: GL; 4. “LR”: LR; 5. “L1”: L1 and L2; 6. “GP”: GP and Ch-S; 7. “WH”: WH6, WH14 and WH52; 8. “N”: N and HS; 9. “Y”: Y and TC; 10. “AA”: AA1, AA2 and AA4; 11. “F”: F and BF; 12. “Gf-J”: Gf-J; 13. “EZ”: EZ; 14. “Lava”: Lava. Not all of these “groups” were completely distinct; weak or variable cross-reactions occurring for particular cultures and antisera during the course of several years of observation suggested a relationship in terms of serotype potentialities, for strains in groups 1 and 2, and in groups 2, 3, 4, 5, and 6. Non-reciprocal cross-reactions are tentatively explained in terms of population fluctuations of serotype within particular cultures; several other suggested explanations remain possible. On the whole, however, the strains remained remarkably stable in dominant serotype.Observations on Tetrahymena in paralyzing antisera, with respect to the extrusion of a gelatinous exudate, in general confirmed previous observations by others. “Chain” formation was noted upon recovery, under conditions suggesting that the chains do not always derive entirely from incomplete cytokinesis of dividing organisms but that at least sometimes an aggregation of separate individuals is also involved. Synchronized division was observed for recovering organisms. A gelatinous material was obtained by centrifugation of a large number of individuals; this material provided a degree of protection to the organisms against antiserum effects while other colloidal materials did not, but the protective effects proved nonspecific in the sense that they were not confined to particular strain-antiserum combinations.

Notes: SYNOPSIS. A rapid quantitative method for measuring trypanostatic activity by means of the nonpathogenic flagellate Herpetomonas culicidarum is described. Of the known trypanocidal agents tested, pentamidine was the most active; stilbamidine and propamidine somewhat less active. H. culicidarum is more resistant to these agents than are some pathogenic hemoflagellates. Two new antifungal antibiotics, nystatin and heptamycin (a candicidin-like antibiotic), had powerful trypanostatic activity in vitro. The potential trypanostatic activity of antifungal agents is noted.

Notes: SYNOPSIS. Approximately fifty % of Natrix piscator from the vicinity of Bombay showed a haemogregarine in the peripheral blood. Schizogonic stages were found in great abundance in the lung capillaries, and occasionally in other internal organs. No parasites could be demonstrated in trombiculid mites of the genus Schongastia fed on infected snakes. Various developmental stages were found in the leech, Hirudinaria granulosa allowed to feed on infected Natrix piscator. The haemogregarine was originally described from this host in Ceylon on the basis of blood stages only and was named Haemogregarina mirabilis. Although the parasite exhibits several of the characters diagnostic of the schizogonic stages of the genus Hepatozoon, it is advisable for the present to retain it in the genus Haemogregarina.

Notes: SYNOPSIS. A new species of a freshwater reticulate dinoflagellate, Woloszynskia limnetica, is described. The membrane structure and the shape of the membrane plates change during cell development. The rod-shaped mitochondria found among the membrane plates disappear in the adult cells; they constitute a center from which starch grains develop. Mitochondria also occur free in the endoplasm. Different physiological activities appear to be performed by morphologically identical chondriosomes. The stigma changes in different phases of the life cycle. The physicochemical properties of the ectoplasm govern the formation of specific structures of the membrane plates, which in turn determine the taxonomic position.

Notes: SYNOPSIS. Pseudomicrothorax dubius, a rather rare protozoon assigned by Kahl to the trichostome order of ciliates, has been found and positively identified for the first time in America, and its morphology and morphogenesis have been studied in detail with the aid of modern techniques. The Chatton-Lwoff silver impregnation method is considered indispensable in acquiring an understanding of the ciliate's infraciliature: both its anatomy in the mature vegetative animal and its activities during the morphogenetics of binary fission.Stomatogenesis is of a complex type, considered here as “semi-autonomous” in nature, although a single, true stomatogenous meridian also is involved. Details of this explicit morphogenetic phenomenon are offered.The presence of a true zone of three adoral membranelles, never before recognized with any accuracy in this ciliate, a buccal cavity and associated structures, and the mode of stomatogenesis have led the writers to propose transfer of the genus Pseudomicrothorax from the Trichostomatida to the order Hymenostomatida.

Notes: SYNOPSIS. Studies of the body ciliature of Balantidium coli and B. caviae (?) after Breslau's opal-blue and Klein's silver nitrate techniques revealed a preoral-dorsal suture area where some of the ciliary rows fail to reach the peristomial margin. The incomplete kineties ranged up to a dozen in number and were variable in arrangement. In a count of 100 specimens of B. caviae (?) the incomplete kineties were at the right of the suture in 39, at the left in 24 and on both sides of the suture line in 37. At the posterior end not many kineties reach the pole but no sutural pattern was seen in that region. Scattered irregularities in the ciliary rows were sometimes seen.Studies of the oral region tend to confirm the view of Fauré-Fremiet that the peristomial ciliature consists of short rows of cilia which are continuations of the anterior body kineties. Membranelles were not found. Thus, some species of Balantidium, at least, show affinities with the Holotricha in agreement with Nie and Fauré-Fremiet.Fission commonly produces two equal-sized daughters but many cases of unequal division were observed. In both these species conjugants are much smaller than vegetative animals and two preconjugant divisions are indicated, the first of which may be unequal.During the early stages of fission, the anterior ends of the kineties of the posterior daughter change direction, becoming oblique in the fission zone. In this region the kinetosomes multiply; possibly some of the kineties also divide but evidence for this is incomplete. No evidence of reorganization at the anterior end of the anterior daughter was seen.Attempts to infect hamsters with B. coli and B. caviae (?) failed. No parasites were found in two collared peccaries repeatedly examined.

Notes: SYNOPSIS. Purification by migration on solid agar plates was studied with a small soil amoeba, Acanthamoeba sp., and a large fresh-water amoeba, Amoeba proteus. Purification seems accomplished largely by two mechanisms: egestion and attrition of contaminating organisms. Digestion may also play a role but probably is less important. The migration method is applicable to motile forms of the two amoebae which differ greatly in volume and motility. Therefore the method may be of potential value in purifying many species. Modifications which should extend the usefulness of the method are considered.

Notes: SYNOPSIS. The gametes of Trichonympha grandis fuse quite differently from those of all the other species of Trichonympha in Cryptocercus; fusion is partial and temporary instead of complete and permanent as in other species. In this species, as in the others, fusion brings about the disintegration of all the extranuclear organelles of the male gamete, but none of those of the female; these persist to become the organelles of the zygote. Gametic union accomplishes two things: loss of extranuclear organelles of male and fusion of pronuclei. Unlike that of the other species of Trichonympha, the cytoplasm of the male gamete of T. grandis contributes slightly, if at all, to the formation of the zygote.

Notes: SYNOPSIS. A new species of Hepatocystis (H. hippopotami) is described from the blood and liver of a Rhodesian hippopotamus (Hippopotamus amphibius). Its relationship with other members of the genus is briefly discussed.

Notes: SYNOPSIS. The role of eleven different types of achromatic figures in chromosomal movement of Barbulanympha is analyzed. When only one pole is present, no chromosomes are ever connected with it, and hence they do not move. The chromosomes go through their usual life cycle including pairing, but remain in the parent nucleus, which, of course, does not divide. When two poles are present with only one pole near the nucleus, the poles, which are the distal ends of the elongate centrioles, do not cooperate in the formation of a central spindle and the chromosomal behavior is just as if there were only one pole—no movement. The same is true when more than two poles are present with only one near the nucleus.Unless a central spindle is present, movement of chromosomes never occurs. However, when many central spindles are present, sister chromosomes may separate and move to poles which are not directly connected by a central spindle. In other words, sisters may separate without moving along a central spindle.In binucleate cells with one central spindle the chromosomes of one nucleus move to the poles, but those of the other do not. Movement always occurs in the nucleus that has its nuclear membrane depressed by the central spindle. When two or more central spindles are present, the chromosomes of both nuclei may move to the poles.

Notes: SYNOPSIS. Euplotes eurystomus Wrzesniowski was cultured on bacterial media with Tetrahymena pyriformis serving as the food organism. Animals were injured with various types of operations using the Chambers' micromanipulator. These animals were followed during the course of their regeneration using various nuclear stains, silver impregnation techniques and vital staining methods. It was found that two cirral fields arose as a result of injury removing one or more of the locomotor organelles and that the posterior field was soon resorbed, while the anterior one replaced all of the old cirri of the regenerating animal. In addition, in response to this sort of injury, complete nuclear reorganization took place. Animals which were injured in a manner not affecting the locomotor organelles directly, responded by proliferating a fine network in the area of injury. This network seemed to reinforce the injured area and persisted until the next binary fission of the animal. No nuclear reorganization took place in these cases.

Notes: SYNOPSIS. The leech, Erpobdella sp., is a suitable invertebrate host for Trypanosoma ambystomae. The developmental cycle involves a mononucleate, rounded body derived from the bloodstream form; this body then transforms into a large plump crithidia. Subsequent divisions yield medium crithidia, small crithidia, and ultimately, metacyclic trypanosomes.

Notes: SYNOPSIS. In diphasic blood agar media Trypanosoma vespertilionis developed spheroid clusters as compared to rather long, sausage-shaped (sometimes branched) clusters formed by Trypanosoma dionisii. The former species attained a greater population density (∼6 × 107 organisms/ml) than the latter (∼ 2 × 107 organisms/ml). Greater numbers of epimastigotes, some in active binary divisions, were observed during the logarithmic phase of growth, and morphologic changes occurred during cultivation which correlated with increased acidity and a depletion of glucose. Maximum numbers of trypomastigote forms were found during the stationary and early death phases. Most of the forms observed after 20 days were sphaeromastigotes. Glucose concentrations decreased to 0 M in T. vespertilionis and to 4.4 × 10−5 M in T. dionisii cultures during the stationary and death phases. By the 12th day of incubation cultures of T. vespertilionis were more acid (pH 5.5) than those of T. dionisii (pH 6.5). No antigenic changes during cultivation of each of the parasites were detected by immunodiffusion. Trypanosoma vespertilionis and T. dionisii contained common and specific antigens. At least 2–3 common antigens were detected in extracts reacted against heterologous antisera. Specific antigens were observed as nonidentical lines formed by extracts reacted against homologous and heterologous antisera and with antisera absorbed with heterologous antigens. At least 2 specific antigens were evident in extracts of T. vespertilionis and 1 in extracts of T. dionisii.

Notes: SYNOPSIS. Five proteins capable of stimulating [3H]thymidine uptake by Trypanosoma cruzi in vitro were isolated from fetal calf serum by (NH4)2SO4 precipitation and ion exchange column chromatography. The proteins were partially characterized by immunodiffusion, immunoelectrophoresis, polyacrylamide gel disc electrophoresis, and SDS electrophoresis. As estimated by SDS electrophoresis, using 4 standards, the molecular weight of protein 1 was 100,000, that of protein 2 was 76,000. and that of proteins 3–5 was 68,000 daltons.

Notes: SYNOPSIS. Amylopectin granules were purified from Eimeria tenella oocysts following digestion with sodium dodecyl sulfate and pronase. The oval granules had a uniform size of 0.5 × 0.7 μm, and consisted of only glucose polymers. α-Amylase treatment yielded 235 nmoles of maltose from the granules from 106 unsporulated oocysts and 93 nmoles maltose from those from 106 sporulated oocysts.Amylopectin phosphorylase activity was detected in the cytoplasm of unsporulated oocysts of E. tenella. It had a specific activity of 13 U/mg protein in crude extracts, and a pH optimum of 6.0. The Km values determined were 9.1 mM for glucose-1-phosphate and 5.6 mM for glucose end groups in potato amylopectin. Enzyme activity declined at a linear rate during sporulation, sporulated oocysts containing less than 8% of the activity of unsporulated oocysts. No amylase-type activity was found in the parasite.

Notes: SYNOPSIS. Plasmodium (Huffia) hermani sp. n. is described from wild turkeys (Meleagris gallopavo Linnaeus) in Florida. It produces rounded schizonts with 6–14 nuclei arranged peripherally as a rosette and elongate, slender gametocytes with irregular margins. Asexual stages parasitize all cells in the erythrocyte series and, in heavy infections, predominantly occur in erythroblasts and their precursors. Presence and degree of pigmentation vary with maturity of the host cell. Gametocytes occupy erythrocytes only, with pigment dispersed in black granules throughout the cytoplasm. Cells containing schizonts are often rounded and enlarged and those parasitized by gametocytes may be somewhat distorted in shape by lateral hypertrophy. Host cell nuclei may be displaced, but are not distorted, except slightly by pressure from the parasite. Plasmodium hermani differs from P. (Giovannolaia) durae by producing low level (〉 6%), nonlethal parasitemias in turkey poults, an absence of phanerozoites in capillary endothelium of the brain and viscera, and inability to infect chicks. Plasmodium hermani is more like P. (Huffia) elongatum in gametocyte morphology, schizogony in all types of erythrocyte precursors, with gametocytes occurring in erythrocytes only, and concentration of schizonts in heavy infections in bone marrow and spleen. It differs from P. elongatum by its lack of infectivity to passeriform and anseriform hosts and by a strong immune response which develops in infected birds.

Notes: SYNOPSIS. Light and electron microscope observations on Dunaliella primolecta Butcher from logarithmic and stationary phases of batch cultures are correlated. Except for the lack of a cell wall the fine structure has typical volvocid features. The transition from logarithmic to stationary phase is marked by changes in content and size of cytoplasmic vacuoles, accumulation of cytoplasmic lipid, accumulation of starch in the plastid matrix, and by the formation of autophagosome-like bodies. The organelles in stationary-phase flagellates are closely packed together because of the cytoplasmic lipid and starch-distended chloroplast. Organisms from logarithmic phase have an abundant ribosome-packed groundplasm supporting the organelles. In the cytochemical demonstration of acid phosphatase activity, Golgi cisternae and smooth and coated Golgi vesicles contain Gomori reaction product. The possible roles of the Golgi apparatus in this flagellate are discussed.

Notes: SYNOPSIS. The succession of morphologic changes in the feeding apparatus (peristome) accompanying conjugation and postconjugant development in the hypotrich Euplotes aediculatus has been examined by scanning electron microscopy (SEM). The details of stomatogenesis inferred from earlier light-microscopic studies of silver-stained preparations have been confirmed and extended.The elaborate peristome is the dominant surface feature of vegetative Euplotes. In conjugation, the ciliates are joined in their peristomial regions; as the conjugants separate, the old feeding apparatus is seen to be disrupted and partially resorbed. In its place is the crescent-shaped primordium of a new peristome, which develops as part of a general cortical reorganization. This primordium expands anteriorly, unfurling a new crown of ciliary membranelles that soon replaces the remaining preconjugant membranellar band. The resulting “exconjugant peristome'’is characterized by a greatly reduced number of adoral membranelles and the absence of paroral membranelles, buccal cavity, and cytostome. Exconjugants thus cannot feed for 2–3 days, until the missing peristomial components are replaced. This occurs by means of a 2nd cortical reorganization, during which new membranelles, developing from another peristomial rudiment, are added directly to the abbreviated exconjugant set. A new buccal cavity is concurrently sculpted as the primordial depression enlarges, and the cells can resume feeding sometime during the 4th day after separation.The implications of this mode of stomatogenesis and the nonfeeding condition are discussed, as are the advantages of SEM for studies of ciliate morphogenesis.

Notes: SYNOPSIS. Monolayers of bovine kidney cells were overlaid with Eimeria magna sporozoites and observed with phase-contrast optics until penetration of the cells by the parasites had begun. Cells and penetrating parasites were fixed with glutaraldehyde and OsO4-containing ruthenium red, dehydrated, and embedded in situ. Cells being penetrated were selected for study in the electron microscope. The lack of intracellular staining with ruthenium red and intact plasmalemmas of cells being penetrated, was accepted as evidence that the sporozoites did not disrupt the plasma membranes. The sporozoite caused invagination of the host cell plasmalemma until the parasite was entirely within the cell, after which the invagination was sealed off by short pseudopodia enclosing the sporozoite within a membrane-lined vacuole inside the cell. Often myelin-forms, apparently of host cell origin, were seen in the space between the sporozoite and the cell.

Notes: SYNOPSIS. California ground squirrels (Citellus beecheyi) were found to be infected with trypa-nosomes whose most striking morphological features are an unusually large kinetoplast and a long, tapering posterior end. The total length is 25.2 μ, and body length is 18.0 μ. This “lewisi”-type species is compared with other trypanosomes reported from American ground squirrels, but a specific diagnosis is not made because the life cycle has not been observed and because morphological features of trypanosomes are known to vary widely under differing environmental conditions.

Notes: SYNOPSIS. The basal apparatus of the flagella and kinetoplast in Leishmania donovani have been studied with the electron microscope. The flagellar fibrils extend into the body of the protozoan to form the kinetosome. At the point of origin of the flagellum, the pellicle invaginates to form a kinetosomal vacuole around the kinetosome. The kinetoplast is formed by a transversely elongated banded structure, surrounded at some distance by a double layered kinetoplast membrane. There is no apparent connection between the kinetosome and the kinetoplast.

Notes: SYNOPSIS. Starvation of Isotricha prostoma for 72–96 hours decreased the cellular amylopectin granules and facilitated the microscopic search for bacterial feeding. I. prostoma selected and ingested only certain rods from among many types of rumen bacteria. In order to isolate the bacteria important as a food source for Isotricha, the starved protozoa were allowed to feed on mixed rumen bacteria, washed, and the crushed protozoan contents quickly cultured for bacteria. Several strains of bacteria were isolated in pure culture. Three of the rod strains isolated were rapidly ingested by I. prostoma when fed to the ciliate. In a monobacterial culture I. prostoma divided once before succumbing.

Notes: SYNOPSIS. Cultures of Trypanosoma theileri were obtained at 36° and at 37.5°C. in a blood-lysate medium inoculated with blood from three dairy cows showing subnormal milk production. The organisms were first seen after 4 days in the first subculture, reached a maximum number of about 500,000 per ml. on the 4th day of the second subculture, and attained about this same number on the 4th day of subsequent transfers. Crithidial forms predominated but trypanosomes of the blood-stream type were also numerous. Cultures were not obtained from cows with normal milk production. The infected cows, although free from helminth parasites, showed a marked eosinophilia.

Notes: SYNOPSIS. A new species of Paramecium, P. jenningsi, n. sp., from South India, is described. It is like P. aurelia except that nuclei are larger, the cell size is somewhat larger, and the macronuclear anlagen (“placentae”) have long-persisting chromatinic centers.

Notes: SYNOPSIS. The nutritional requirements of 3 isolates of Prymnesium parvum (2 Israeli, 1 Scottish) included vitamin B12 and thiamine. For comparison, 2 other brackish chrysomonads were studied: Monochrysis lutheri isolated by Droop in Scotland and Isochrysis galbana purified by McLaughlin from a culture obtained from the Plymouth laboratory.The isolates of Prymnesium parvum and Isochrysis galbana had a molecular B12 specificity like Ochromonas malhamensis: no response to Factor B, pseudovitamin B12, Factor A or Factor H. M. lutheri, in contrast, responded to pseudovitamin B12, Factor H, and Factor A.Thiamine was essential; 1.0 μg.% allowed full growth of P. parvum. The NaCl concentration for good growth was 0.3–5.0%; growth was possible from 6–12%. Dark growth was not achieved.Ammonia, as suggested from its use in suppressing outbreaks of P. parvum, was sharply inhibitory, less so at high concentrations of NaCl or at acid pH.Nitrate, ammonia, arginine, asparagine, methionine, histidine, alanine, glycine, serine, proline, leucine, isoleucine, tyrosine, aspartic and glutamic acids, acetylurea, and creatine served as nitrogen sources in both acid and alkaline media.The phosphate requirement of P. parvum and M. lutheri and Isochrysis galbana was satisfied by inorganic phosphate, commercial glycerophosphate, yeast adenylic acid, cytidylic acid, monoethyl phosphate, and riboflavin monophosphate.Laboratory cultures in defined media of the isolates of P. parvum were toxigenic to Lebistes and Gambusia. Culture fluids from alkaline media were more toxic than those from acid media, as previously noted in Israel.Culture media suitable for production of large quantities of these organisms were developed.

Notes: SYNOPSIS. Certain aspects of the metabolism of a Trichomonas batrachorum-type flagellate from the cecum of swine were studied. This trichomonad (1) oxidized glucose, mannose, maltose, sucrose, and inulin, (2) was incapable of oxidizing Krebs' cycle intermediates, (3) possessed peroxide-splitting capabilities, (4) was inhibited by only iodoacetate and arsenite, and (5) formed acid(s) aerobically. Although there was no effect on oxygen uptake, pyruvate and lactate increased the anaerobic evolution of gas(es). In addition to CO2, other gas, not absorbed by KOH, was produced anaerobically.Compared with other porcine trichomonads, the metabolism of this small trichomonad resembles most closely that of the large cecal trichomonad, T. suis. However, the smaller trichomonad had a generally lower respiratory rate, a slightly lower optimal pH, and failed to oxidize fructose, galactose, lactose, raffinose, and trehalose.

Notes: SYNOPSIS. The “dry” silver method is redescribed with special attention to the possible difficulties encountered in its use. This method first revealed the silverline or neuroformative system of the ciliates, and is considered the best method for the demonstration of this structure. The valuable results obtainable with this technique are pointed out and illustrated with appropriate photomicrographs.

Notes: SYNOPSIS. It has been assumed by others that green euglenas and derived bleached forms are physiologically equivalent except for chlorophyll and plastids. Some workers, however, have remarked upon differences which might depend on the mode of bleaching.Several hitherto undescribed chlorotic substrains of E. gracilis var. bacillaris were examined for pigment alteration, growth under a variety of conditions, and ability to withstand high temperature. These studies indicated physiological variation in the different chlorotic substrains. Although all were apparently chlorophyll-less and aplastidic, only one seemed completely achromatic. The carotenoid content of others varied. Metabolic changes manifested by altered pigmentation may reflect enzymatic variation caused by the chlorosis-inducing agents.

Notes: SYNOPSIS. Thin sections of Amoeba proteus, fixed in osmium tetroxide and embedded in methacrylate, were examined in the electron microscope. The fine structure of various protoplasmic components is described. The plasmalemma, or cell membrane, varies in thickness and structure. These variations may be due to variations in physiological state, or they may be due to differences in preparation. Along its cytoplasmic edge is always present a definite line approximately 0.01 to 0.02 μ thick. The mitochondria, or beta granules, exhibit a structure similar to that of the mitochondria of several other protozoa and comparable to that of the mitochondria of other animals. In definite association with the membrane of the food vacuole are dense, rounded particles which in size are below the limit of resolution of the light microscope. Such dense particles are much less frequently present in the hyaloplasm and in association with the plasmalemma. A possible relationship to the neutral red granules associated with food vacuoles of Paramecium is suggested. The contractile vacuole possesses a thin membrane surrounded by a much thicker circum-vacuolar zone of irregular strands which may form a three-dimensional network around the membrane. This may represent the contractile element of the vacuole. A single layer of mitochondria is closely apposed to the circum-vacuolar zone. Many small vacuoles and irregular vesicles are present throughout the cytoplasm. At times there occur groups of small, thin-walled vesicles, which may correspond to an endoplasmic reticulum. The nuclear envelope consists of a thick inner porous layer and a thinner outer layer that is continuous yet is marked by the presence of numerous small annuli, each apparently surrounding a pore. In its structure, this outer layer appears to correspond to the entire nuclear envelope of many other cell forms.

Notes: SYNOPSIS. Irradiation of Stentor coeruleus with Xray doses of 150–300 kr inhibited growth in size and fission. The irradiation also led to the development of structural abnormalities, which appeared about a day after irradiation. The inhibition of growth and fission was independent of the oxygen concentration during irradiation, but the abnormalities were produced at lower doses in nitrogen than in air. Regeneration of parts removed by cutting occurred even at the highest doses at essentially normal rate even during the period when over-all growth was completely inhibited. The conclusion is drawn that delay in fission by radiation is a secondary consequence of inhibition of growth and not a consequence of blocks in the specific morphogenetic processes required for division.

Notes: SYNOPSIS. A description is given of the formation of an unusual type of achromatic figure by two very long, narrow centrioles. The unique manner in which this structure functions in chromosomal movement is explained.

Notes: SYNOPSIS. Oocysts and endogenous stages of new species of Eimeria and Isospora from the house lizard, Gehyra mutilata, are described. The ellipsoid to subspherical 2-layered oocysts of E. cicaki averaged 24.0 × 21.0 μm. Polar granules are present. Micropyle and oocyst residuum are absent. Ellipsoid sporocysts average 12.2 × 9.0 μm. A sporocyst residuum is present, but the Stieda body is absent. Endogenous stages are in epithelial cells of the small intestine. The subspherical single-layered oocysts of I. thavari average 23.8 × 22.8 μm. The polar granule is present; micropyle and oocyst residuum are absent. Ellipsoid sporocysts average 12.8 × 9.4 μm. Stieda body and sporocyst residuum are present. There are endogenous stages in epithelial cells of the small intestine.

Notes: SYNOPSIS. Oocysts of Eimeria natricis sp. n. and Eimeria sipedon sp. n. were isolated from 2 Northern Water Snakes, Natrix sipedon sipedon (Linnaeus), in Iowa. Oocysts of E. natricis were elongate, slightly ovoid, averaging in size 32.3 × 17.5 μm; sporocysts averaged 15.7 × 8.2 μm. Oocysts of E. sipedon were broadly ovoid averaging in size 18.0 × 15.9 μm; sporocysts averaged 12.0 × 7.4 μm. In both species, sporocyst residua were present, but micropyles, polar granules and oocyst residua were lacking.

Notes: SYNOPSIS. Oocysts of Isospora serini and Isospora canaria, from the canary Serinus canarius, were broken, added to a cell suspension, fixed in Karnovsky's fluid, and studied in the electron microscope. The oocyst wall of each species had an electronlucent inner layer, a more osmiophilic middle layer and an outer layer of electron-lucent (I. serini) or electron-dense material interspersed with some electron-lucent material (I. canaria). A few, relatively large lipid-like bodies were present in the outer or middle layer of the oocyst wall of I. canaria. As many as 9 membranes were present in the oocyst wall of I. canaria and 3 in that of I. serini. When exposed to a trypsin-sodium taurocholate fluid, sporozoites of I. serini excysted from 5-month-old sporocysts in vitro, but not from sporocysts stored for more than 6 months. No excystation occurred in 15-month-old I. canaria sporocysts. Similarities and differences in excystation between I. serini and other Isospora, Eimeria, and Sarcocystis species are discussed.

Notes: SYNOPSIS. The shock reaction of Euglena gracilis strain Z to a sudden increase in light intensity (the “direct photophobic response”) was examined by high speed cinemicrography. The response is expressed as a turning reaction toward the dorsal side of the cell, after a transduction time of 0.1–0.5 sec after the onset of stimulation. Transduction times, turning rates, and flagellar beat frequencies were measured by analyzing the filmed sequences. The experimental data are consistent with a mechanism of directional homeostasis in negative phototaxis that is based upon shading of the photoreceptor by the cell's posterior end.

Notes: Book reviews in this article:Starr, M. P., Ingraham, J. L. & Raffel, S., eds. 1975. Annual Review of Microbiology.

Notes: SYNOPSIS. Data for host and geographic distribution are listed for Pirhemocyton and for apparently similar infections of poikilothermic vertebrates. The list was compiled from published accounts of Pirhemocyton, Toddia, Cytamoeba, Bertarellia, Piscine erythrocytic necrosis, Immanoplasma, Haematractidium, Sauroplasma, Sauromella, Serpentoplasma, Tunetella, Haemohormidium and unnamed infections. New records are included for Pirhemocyton and Haematractidium. The probability that some may be viruses and not protozoa is discussed; Haematractidium is shown by electron microscopy to be a eukaryote whereas Immanoplasma is not a eukaryote.

Notes: SYNOPSIS. Relationships between the cell cycle and the beginning of conjugation were analyzed for 3 hypotrichs: Diophrys scutum, Oxytricha bifaria, and Euplotes crassus. The first 2 species enter conjugation with micronuclei in G1; the latter species with a micronucleus in G2. The 1st micronuclear division of conjugating E. crassus is mitotic. Thus meiotic DNA replication occurs when the cells of each species have already entered the mating process.Cells from asynchronous populations start conjugation with their macronuclei primarily in G1 or more rarely at the beginning of the S stage in a percentage significantly different from that expected on the basis of random mating among all cells in the population. Also, macronuclear replication, when already begun, was blocked in cells undergoing conjugation. Therefore only the G1 or the very early S stages of the cell cycle are compatible with conjugation in the 3 analyzed species.

Notes: SYNOPSIS. Twenty different isolates of the cellular slime mold Acrasis rosea, obtained from diverse sources and geographic regions, were studied to determine similarities and differences in their development and structure in culture and their sensitivity or resistance to selected chemicals incorporated into the culture media. Six different classes of fruiting were defined based on the size, distribution, and type of sorocarps formed on the yeast, Rhodotorula, streaked on agar. In the course of these studies a significant mutant, NC-18V (variant), developed spontaneously from the wild type, normal parent strain NC-18N. The mutant differed considerably from all other Acrasis isolates, appeared several times in purified parental cultures, and represents the first laboratory derived variant of A. rosea to be described. Purified strains of the variant (V) and normal (N) cultures were obtained by single-spore isolation. Normal and variant amebae were mixed in ratios of 10:1 and 100:1 (N:V) and spore and stalk cells were selected from different sorocarps in various regions of the culture plate for analysis. The results of these selection experiments clearly indicate that the individual variant amebae have increased migratory ability and that they develop smaller, morphologically different, and more numerous sorocarps that form at distances further from the food source than NC-18N. Some isolates of Acrasis no longer were able to fruit and were classified as “non-fruiters” and a few other isolates formed only a few, small sorocarps on rare occasions. These isolates were mixed together in various combinations of 2 and 3 to screen for cell interaction, but no synergism contributing to fruiting was found. Although fruiting of many A. rosea isolates was inhibited by exposure to continuous light or constant darkness, some “escape”fruiting was noted in certain isolates even when small inocula were used. Single spore isolates of these escape fruiters still fruited in continuous light or dark, but fruiting was always greatly enhanced by a routine 12 hr light : 12 hr dark incubation cycle. It was shown by biochemical studies that actidione, crystal violet, malachite green, ethyl violet, and 5-fluorodeoxyuridine selectively killed some isolates and permitted a classification of isolates as either sensitive or resistant. In a further study of cell interaction between 2 different sets of Acrasis isolates with contrasting biochemical and morphologic markers the formation of neotypes or recombinants could not be demonstrated.The results of this study clearly indicate the existence of significant variation in A. rosea and the potential for application of these differences to developmental studies.

Notes: SYNOPSIS. The ultrastructure of promastigotes of 4 reptilian isolates of Leishmania grown in culture, is described. One mammalian isolate of Leishmania is also examined for comparison. No differences in the basic ultrastructure of these strains are apparent; neither is there any significant digression from the organization described for other trypanosomatids. It appears, however, that the numbers of subpellicular microtubules are of potential use in taxonomy, and that differences in the spacing of these organelles exist between reptilian and mammalian forms. In addition, an attempt is made to clarify aspects of attachment of the flagellum to the subpellicular tubule network, and to the anterior face of the kinetoplast. Finally, the formation of multivesiculate bodies from the Golgi apparatus is described, together with some features of dividing forms.

Notes: SYNOPSIS. Alveolar membranes and an epiplasm exist under the cell membrane of the noncontractile heterotrich ciliate Climacostomum virens. Postciliary microtubular ribbons join at the right of each somatic kinety to form a Km fiber. Two transverse microtubular fibers occur per kinetosomal pair. A myonemal network interconnects the kinetosomal bases intrakinetally and interkinetally. Ultrastructural comparisons are made between the contractile and noncontractile heterotrichs.The buccal cortex consists of an adoral zone of membranelles, a peristomal field, a buccal tube, the apical membranelles, and a haplokinety. The kineties of the peristomal field and buccal tube are rows of paired kinetosomes, with a postciliary ribbon of microtubules arising from the posterior kinetosome of each pair, and a transverse ribbon and an oblique ribbon from the anterior kinetosome. No Km fibers exist in this region. The haplokinety is a collar of paired kinetosomes surrounding the cytostome; a postciliary microtubular ribbon descends from each kinetosomal pair into the cytostomal region. Ultrastructural details of the buccal cortex of C. virens and other heterotrichs are compared. The nemadesmata which lie under the membranelles are implicated in the body bending of C. virens.Algae endosymbiotic in the cytoplasm of C. virens are described.

Notes: SYNOPSIS. Crosses between serine requiring and non-requiring clones from natural habitats give rise to progeny that are numerically equally distributed between the two categories. Most of the progeny from crosses between two serine requiring parental clones require serine with a few segregating out that do not need the amino acid. These data indicate that the gene or genes controlling the serine non-requirement are recessive to the wild type which requires serine. Growth of the F1 progeny was highly variable. Some clones failed to survive on serine deficient media and were therefore tentatively assigned the genotype +/+. The remaining clones were of two classes: one grew slowly on serine deficient media and was given the genotype of the heterozygote, +/s; the other grew without serine, hence was given the double recessive genotype, s/s. The F2 progeny from matings of s/s and s/s need no serine whereas the cross of +/s and s/s gave equal numbers of serine requiring and serine non-requiring progeny. The cross of two heterozygotes, +/s and +/s, yield progeny approximating the 3:1 ratio in favor of serine requiring clones. Crosses at the F3 level produced non-viable offspring in all cases except one. Progeny from this cross with the genotype s/s were mated giving rise to F4 progeny all of which grew without serine. The data support an outbreeding economy for this organism with selection in favor of the heterozygote. Although the data seem to favor a single-gene hypothysis, suppressor genes may be involved. With selection favoring the heterzygote, distorted genetic ratios make the data difficult to analyze.

Notes: SYNOPSIS. Intracardial inoculation of 1–10 million L. donovani in 0.1 ml. of ground spleen suspension from an infected animal (hamster) results in a uniform rise of parasite numbers in the untreated animal over the first 8 days after the inoculation. This rise is highly consistent from experiment to experiment.Treatment is accomplished by parenteral injection of a compound for 6 successive days in this time interval, starting 24 hours after inoculation.No known active compound in proper dosage (sodium stibogluconate, pentamidine, fuadin) has failed to show a significant suppression of the expected rise in parasite numbers. No known inactive compound has had any effect on the course of the infection.The dosage-response curve for the active compounds suggests that the method is a sensitive one. Since it takes only 8 days to complete, it is economical as well.

Notes: SYNOPSIS. It has been shown that the output of the contractile vacuole of Crithidia fasciculata increases as the concentration of solute in the external solution decreases when NaCl is the solute. The increase in output is the result of increased rate of growth as well as increased maximum size, the latter being more important in the range 0.1M–0.01M. Solutions of penta-erythritol produce the same effects as isosmolar solutions of NaCl. Body volume is not maintained constant but increases less than two-fold between 0.1M and 0.0001M. The isotonic concentration of NaCl is estimated as 0.12M. It is not possible to demonstrate any effect of concentration of the external environment on the endogenous rate of oxygen consumption. A linear relationship between output and calculated osmotic gradient across the cell membrane has been shown in the concentration range 0.1M–0.01M. Absence of this relationship, and failure of body volume to increase as predicted, in solutions more dilute than 0.01M are interpreted as indications that other processes probably become predominant in these solutions. It is concluded that the contractile vacuole of this flagellate is incapable of maintaining absolute constancy of internal osmotic pressure and body volume but prevents much of the change expected on physical grounds.

Notes: SYNOPSIS. The rather rarely found holotrichous ciliate Pseudomicrothorax dubius, generally considered in the most authoritative literature to be a member of the order Trichostomatida, more likely belongs in the Hymenostomatida. Its curious combination of trans-ordinal characteristics, however, makes difficult exact systematic allocation of it and of the congeneric species P. agilis. The provocative morphological features include: a gymnostome-like cytopharyngeal “basket”; a tetrahymenal buccal apparatus, with membranelles comparable with those of primitive hymenostomes; an advanced semi-autonomous type of stomatogenesis; and sensory bristles, flattened rigid form, and restricted ciliature reminiscent of certain spirotrichs. Brief discussion is presented concerning the influence of modern ideas of ciliate classification upon what is considered the proper taxonomic position of the genus.

Notes: SYNOPSIS. A new fresh water species of Actinosphaerium is described, the fourth member of the genus. Some of the more significant of its diagnostic traits are: 1) the Actinophrys-like nuclei with peripheral nucleolar granules and without central rosette-shaped nucleoli, 2) the occurrence of some nuclei in the ecto-endoplasmic border and the insertion of axial filaments on them, and 3) the low ratio of endoplasm to ectoplasm.

Notes: SYNOPSIS. In cultures of the marine dinoflagellate Gonyaulax polyedra grown with alternating light and dark periods of 12 hours each, at least 85% of all cell divisions which occur in a day take place during a 5-hour period spanning the end of the dark period and the beginning of the light period. A very distinct maximum in the number of recently divided cells occurs at about the time the light period begins.This diurnal periodicity in cell division is lost after 4 to 6 days in continuous bright light, but will persist for at least 14 days in continuous dim light. The period of approximately 24 hours under constant conditions is only slightly altered by varying light intensity and temperature, both of which factors are known to affect markedly the generation time. The time at which cell division occurs is therefore postulated to be controlled by some sort of rhythmic or clock mechanism.Similarities between the cell division rhythm and the endogenous rhythm of luminescence in this organism are discussed. The occurrence of a glow, or steady light emission of low intensity, at about the time of cell division, is described, and it is suggested that this glow may result from cellular changes accompanying certain stages of cell division.

Notes: SYNOPSIS. The photographs illustrate male and female gametes before fertilization, several progressive stages in the entrance of the male gamete into the cytoplasm of the female, cytoplasmic fusion of gametes, loss of extranuclear organelles of male gamete, retention of extranuclear organelles of female gamete, movement of pronucleus of male gamete to that of female, progressive stages in fusion of pronuclei, and the formation of the zygote which possesses the extranuclear organelles of the female gamete. Some abortive attempts at fertilization, resulting from failure of gametes to differentiate, are shown.

Notes: SYNOPSIS. Detailed directions are given for the preparation of a simplified assay medium and of natural materials for assay of pteridines with Crithidia fasciculata. Unconjugated pteridines in natural materials which also contain conjugated pteridines (folic and folinic acids) can be assayed by destroying the conjugated pteridines with acid hydrolysis, which does not appreciably alter Crithidia-active unconjugated pteridines. The widespread occurrence of unconjugated pteridines and their significance in such processes as photoreception are discussed.

Notes: SYNOPSIS. Photokinesis or the non-directed rate of swimming of Euglena gracilis for various light intensities was studied. The rate of swimming in white light was found to increase with light intensity until it reaches 0.16 mm./sec. at a saturation of 40 ft. candles, and then decreased with increasing light intensities. Polarized light appeared to be more effective (0.18 mm./sec. at 13 ft. candles) than non-polarized light.The action spectrum for photokinesis showed two peaks, a major one near 465 mμ, and another in the neighborhood of 630 mμ, having the values of 0.18 mm./sec. and 0.16 mm./sec. respectively at an intensity of 4 ft. candles.The action spectrum for phototaxis, or directed orientation, had a peak near 420 mμ and showed a maximum near 490 mμ. Both dark-grown and dark-adapted Euglena showed spectral peaks similar to those of the light-grown cells. For polarized light, the action spectrum had two additional peaks at 468 mμ and 508 mμ. The polarized light effect may indicate more than one light-absorbing pigment within the “eye spot” or that other pigments within Euglena were absorbing.

Notes: SYNOPSIS. Four new species of Eimeria are described from small mammals in Liberia. These are: E. levinei, sp. nov. from a free-tailed bat, E. firestonei, sp. nov., and E. milleri, sp. nov., from a shrew, and E. putevelata, sp. nov., from a striped grass mouse.

Notes: SYNOPSIS. A new species of Stentor is described, a fresh water form, medium sized, with cerulean blue pigment, and characterized by retractable feeding organelles.

Notes: SYNOPSIS. Coprozoic protozoa from elk, bison, bear, moose, coyote, marmot, cattle, horse, sheep and man were kept in feces at 4° C. for 2–6 months. During that time in most of the samples there developed the flagellates Cercomonas sp., Copromonas ruminantium and Monas communis; the amoebae Vahlkampfia sp. and Sappinia diploidea, and ciliates of the Nyctotherus type, and an unidentified smaller species. There was a correlation between numbers of protozoa and bacteria. The same species of protozoa in soil or in soil mixed with boiled feces failed to live. Coprozoic protozoa may require certain essential metabolites from bacteria as do true parasites. The wide variation in appearance of cysts made it practically impossible to identify the protozoa with certainty in that stage. Reliance had to be on motile forms which readily developed in the cold cultures.

Notes: SYNOPSIS. Ciliate protozoa from the rumen of the tsessebe, Damaliscus lunatus lunatus, all belong to the family Ophryoscolescidae and no holotrichs were found in any of the 16 animals. Eighteen species were identified of which Entodinium fyferi sp. n., Enoploplastron garstangi sp. n. and Epidinium lunatus sp. n. are new and have been described for the first time. A short redescription of Eremoplastron gigantium Kofoid & MacLennan is given.

Notes: SYNOPSIS. A microsporidan tentatively classified as Encephalitozoon sp. on the basis of structure and tinctorial qualities was identified in tissues from a group of blue-masked lovebirds, Agapornis personata (Reichenow). The organism was present in renal tubular epithelial cells, hepatocytes, bile duct epithelial cells, and intestinal epithelial cells. Focal hepatic necrosis occurred around clusters of the organisms but inflammation was minimal or absent in the other infected tissues. Attempts to infect laboratory mice with the organism were unsuccessful. Ultrastructural features were compared with those of E. cuniculi of mammals.

Notes: SYNOPSIS. The phototactic orientation of the dinoflagellate Gyrodinium dorsum was examined using photomicrographic, cinematographic, and closed-circuit television technics. Particular emphasis was placed on examining the movements and possible roles of the flagella during orientation. The data suggest that the longitudinal flagellum is primarily responsible for phototactic orientation, while the lateral flagellum is involved in forward propulsion and cell rotation. A possible receptor mechanism is proposed by which light direction sensing is accomplished.

Notes: SYNOPSIS. Secondary lysosomes of cultured mouse peritoneal macrophages were labeled with the electron-dense colloid saccharated iron oxide; the identity of the labeled structures was checked by the Gomori reaction for acid phosphatase. Amastigotes of Leishmania mexicana mexicana derived from mouse lesions were used to infect these macrophages in vitro. In electron micrographs of thin sections of infected macrophages the labeled secondary lysosomes were seen fused with the parasitophorous vacuoles without preventing subsequent multiplication of the parasites. A similar fusion probably occurs in vivo, and may provide a pathway through which not only nutrients but also drugs and host antibodies could reach the intracellular parasite.

Notes: SYNOPSIS. Tintinnida of the New York Bight (a bend in the coastline) were identified during the 1-year period August 1973–August 1974. Recurring genera included Stenosemella and Tintinnopsis; seasonal genera were mainly the hyaline Favella, Metacylis, and Helicostomella; exotic or unusual genera included Parafavella and Ptychocylis. Large size differences in loricae were found seasonally, related apparently, to water temperature.

Notes: SYNOPSIS. In Paramecium caudatum, occurrence of macronuclear regeneration is closely related to the time of feeding after conjugation. Macronuclear regeneration is induced with a high frequency when conjugating pairs are transferred into fresh culture medium. Feeding immediately after conjugation induces early cell division and 3 or more fissions occur without macronuclear division because of the inability of the macronuclear anlagen to divide. In the cells lacking normal macronuclear anlagen, old macronuclear fragments undergo regeneration and form vegetative macronuclei.

Notes: SYNOPSIS. An in vitro system, based on the rocker dilution technic, has been developed that supports intraerythrocytic growth of a rat-adapted strain of Plasmodium vinckei chabaudi from ring to schizont stages; some reinvasion was obtained, although invariably, this was associated with a decrease in parasite numbers. Pertinent features were the very high buffer content of the medium and the low oxygen tension of the gaseous phase. Lactate production, glucose utilization, and 3H-leucine and 3H-adenosine incorporations were investigated for their suitability to monitor parasite growth. Throughout an 18-hr incubation there was a continuous and increasing production of lactate and utilization of glucose, which correlated well with the development of the parasites from ring to schizont stages. During the same period, there was a low but continuous and increasing incorporation of 3H-leucine into parasite protein. However, 3H-adenosine was incorporated only for the 1st hr of incubation, after which time no net incorporation occurred. Parasites grew normally from ring to schizont stages even in the absence of adenosine from the dilution medium.

Notes: SYNOPSIS. Monomeric ribosomes, isolated from the monkey malaria Plasmodium knowlesi by the combined use of low concentrations of Triton X-100 and differential centrifugation, sedimented in the SOS range and could be dissociated into 60 and 40S subparticles. The base composition of the rRNA was typically protozoan; that is, low in guanine and cytosine residues.

Notes: SYNOPSIS. The life cycle of Eimeria ferrisi is described from experimentally infected Mus musculus. The prepatent period was 3 days and the patent period was 3–4 days. The endogenous stages were found only in the cecum and colon. Three generations of schizonts were found. Mature 1st-generation schizonts first seen 24 hr postinoculation (PI) measured 10.9 (7–14) × 10.2 (6–13) μm and had 9.6 (7–14) merozoites. Some 2nd-generation schizonts had uninucleate merozoites and others had multinucleate merozoites. The former were first seen in small numbers 36 hr PI and were most abundant 48 hr PI. They measured 9.6 (5–13) × 7.9 (6–12) μm and had 18 (6–25) merozoites. Schizonts with multinucleate merozoites were seen 72 hr PI. Mature 3rd-generation schizonts were seen 72 hr PI. They measured 14.0 (12–18) × 11-0 (9–13) μm and had 12.5 (5–16) merozoites. Macrogamonts were first seen in 72 hr sections. Each young macrogamont had a large nucleus with a prominent nucleolus. Only one type of cytoplasmic granule appeared to be involved in the formation of the oocyst wall. Mature macrogamonts were 11.0 (5–14) × 10.0 (6–13) μm. Crescent-shaped bodies were observed in the parasitophorous vacuole of trophozoites and young macrogamonts. Early microgamonts were first recognized at 96 hr by the presence of darkly stained and irregularly shaped nuclei. Usually, mature microgametes were arranged in long, narrow whorls at the periphery of the microgamont or in whorls at the surface of 2–5 compartments.

Notes: Book reviews in this article:Hedley, R. H. & Adams, C. G., eds. 1974. Foraminifera.

Notes: SYNOPSIS. Ultrastructure of cysts of Naegleria gruberi, Naegleria fowleri, and Naegleria jadini was compared by transmission electron microscopy. Pores in the cyst wall were observed in all 3 species. In N. gruberi they were surrounded by a collar and sealed with a relatively large mucoid plug; no such collar was seen around the pores in the other 2 species, in which the plug was smaller than that in N. gruberi. An electron-dense plaque serving as an additional pore closure was present in all 3 species. In N. gruberi, the cyst wall consisted of an inner thick and an outer thin layer; however, only the inner component was present in cysts of N. fowleri and N. jadini, which had a smooth appearance. At the ultrastructural level, excystment of N. fowleri involved digestion of the mucoid plug and emergence of the trophozoite through the pore. Some digestion of the cyst wall also appeared to take place during excystment.

Notes: RESUME. La Microsporidie Nosema bombycis, Protozoaire parasite agent de la pébrine du ver à soie, a étéétudiée cytochimiquement à la fois en microscopie photonique et électronique.Les examens ont porté sur la détection et la localisation des acides nucléiques (ADN et ARN), des polysaccharides, de la phosphatase acide, au cours des différents stades du développement dans les cellules de I'hôte (du schizonte à la spore).Les principaux résultats concernent les observations relatives aux polysaccharides et à la phosphatase qui ne sont détectés qu'au stade de la spore et ne sont pas observés au stade du schizonte. Les polysaccharides sont présents au niveau du sac polaire, du filament polaire et sur la membrane cytoplasmique; la phosphatase acide est localisée au niveau du sac polaire, du filament polaire et dans la vacuole postérieure.SYNOPSIS. Nosema bombycis, agent of pebrine disease of silkworm, was studied cytochemically, using both light and electron microscopy. Presence of nucleic acids (DNA and RNA), polysaccharides, and acid phosphatases was demonstrated and localization of these substances was determined in various stages of the parasite (from the schizont to the spore). DNA and RNA were detected in all these stages. Polysaccharides and acid phosphatase were found in the spore but not in the schizogonic stages. Polysaccharides were detected in the polar cap, the polar filament, and the limiting membrane of the cytoplasm of the spore. Acid phosphatase was found in the polar cap, the polar filament, and the posterior vacuole.