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: The development of an automated photographic measuring system (APM) is described. A very accurate laser beam scanning microdensitometer is used to digitise the photographic plate and a series of on line computers analyses the data during scanning. The system is available as a national facility for United Kingdom astronomers and guest investigators.〈section xml:id="abs1-2"〉〈title type="main"〉RésuméOn décrit un systéme automatisé de saisie de données sur cliché. Un microdensitométre à laser numérise la plaque photographique et les données sont analysées en temps réel par ordinateur. Le systeme est destiné aux astronomes du Royaume Uni et aux chercheurs y séjournant.〈section xml:id="abs1-3"〉〈title type="main"〉ZusammenfassungBeschreibung eines automatisierten photographischen Messsystems (APM). Ein hochgenaues Laser-Mikrodensitometer wird dabei zur Digitalisierung der Bilder benutzt, undeine Serie von On-line-Rechnern analysiert die Daten während der Abtastung. Das System steht für Astronomen im Vereinigten Königreich und anderen Forschern zur Verfügung.

Notes: Two complementary measuring instruments are described which use a very simple principle and which take three dimensional measurements or plots directly from small objects. The first instrument can achieve accuracies of ± 0·3 mm on objects whose largest dimension is 300 mm. The second can achieve ± 0·02 mm on objects smaller than a 25 mm cube.〈section xml:id="abs1-2"〉〈title type="main"〉RésuméOn présente deux instruments de mesure complémentaires el de principe très simple permettant de relever dans l'espace des coordonnées sur de petits objets, le premier avec une exactitude de ± 0.3 mm sur des objets de dimension inférieure à 300 mm, le second avec une exactitude de ± 0.02 mm sur des objets de dimension inférieure à 25 mm.〈section xml:id="abs1-3"〉〈title type="main"〉ZusammenfassungBeschreibung von zwei Zusatzmessgeräten, die auf einem sehr einfachen Prinzip beruhen und mit denen dreidimensionale Messungen oder Auswertungen von kleinen Objekten direkt durchgeführt werden konnen. Mil dem ersten Gerät kann eine Genauigkeit von ± 0,3 mm bei maximalen Objekt abmessungen von 300 mm und mit dem zweiten von ± 0,02 mm bein Objekten, die kleiner als ein 25 mm-Kubus sind, erreicht werden.

Notes: This paper outlines the technical procedures used in commercial orthophotomap production and attempts to identify some of the main differences in technical approach between orthophotomapping and conventional line mapping.〈section xml:id="abs1-2"〉〈title type="main"〉RésuméOn décrit les techniques industrielles de production d'orthophotocartes et on compare leur emploi avec celui des techniques classiques.〈section xml:id="abs1-3"〉〈title type="main"〉ZusammenfassungSkizzierung der Technologien, die bei der kommerziellen Herstellung von Orthofotokarten angewendet werden, wobei versucht wird, die hauptsächlichen Unterschiede der Techniken zur Herstellung von Orthofotokarten und konventionellen Strichkarten aufzudecken.

Notes: This paper investigates the effect of the deviation of measured points from the standard locations when carrying out a relative orientation of a stereomodel. The analytical solution of more than 100 cases was considered and, for each case, the weights for the elements of relative orientation and the correlation coefficients were evaluated. The stability of the solution was studied by calculating the characteristic roots of the matrix of normal equations.It is shown that, theoretically, the solution of the relative orientation problem can always be achieved whenever the locations of the measured points satisfy stated geometrical requirements. However, the reliability of the solution depends on their exact positions in the stereomodel. When the accuracy is too low, in practice there is no solution.〈section xml:id="abs1-2"〉〈title type="main"〉RésuméOn étudié l'effet sur l'orientation relative d'un couple de variations de position des points de base. Plus de 100 cas ont été considérés et à chaque fois ont été estimées les précisions des paramètres calculés ainsi que leur correlation. On a de plus, étudié la stabilité de la solution par l'intermédiaire des valeurs propres de la matrice normale.Il n'est pas indispensable, en principe, d'imposer de contraintes précises au choix des points de base; mais de ce choix dépend la fiabilité de la solution, faible s‘il est par trop fantaisiste.〈section xml:id="abs1-3"〉〈title type="main"〉ZusammenfassungIn der Arbeit wird der Einfluss der Abweichung der gemessenen Punkte von ihrer Standardlage bei relativer Orientierung eines Stereomodells untersucht. Dazu werden mehr als 100 analytische Lösungen analysiert und für jeden Fall die Gewichte der Elemente der relativen Orientierung und die Korrelationskoeffizienten berechnet. Die Stabilität der Lösung wurde durch Berechnung der charakteristischen Wurzeln der Matrix der Normalgleichungen abgeschätzt.Es wird gezeigt, dass theoretisch immer die Lösung des Problems der relativen Orientierung erreicht werden kann, sobald die Lage der Messpunkte die geometrischen Anforderungen erfüllt. Die Zuverlässigkeit der Lösung hängt jedoch von der exakten Lage der Punkte ab. Wenn ihre Genauigkeit zu gering ist, gibt es praktisch keine Lösung.

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: An automatic plotting instrument development is described where the coordinate corrections are introduced in the optical system and not at the photograph. It is suggested that the opto-mechanical devices used for correction and the proposed use of microprocessors for control of these devices offer the possibility of producing a low cost automatic plotter and stereocomparator.〈section xml:id="abs1-2"〉〈title type="main"〉RésuméOn decrit une solution au probléme de la correction des coordonnées cliché pour le restituteur analytique et le stéréocomparateur: ces corrections sont introduites dans la partie optique du système et commandées par l'intermédiaire de microprocesseurs. Ceci devrait permettre d'abaisser le coût de ce type d'appareil.〈section xml:id="abs1-3"〉〈title type="main"〉ZusammenfassungBeschreibung eines automatischen Auswertegerätes, bei dem die Koordinatenkorrekturen nicht den Bildträgern, sondern dem optischen System zugeführt werden. Es wird angenommen, dass die zur Korrektur verwendeten optisch-mechanischen Vorrichtungen und die vorgeschlagene Verwendung von Mikroprozessoren zu deren Steuerung die Möglichkeit zum Bau eines billigen automatischen Auswertegerätes und Stereokomparators bieten.

Notes: The paper deals with the analytical plotter and its impact on numerical photogrammetry. A short introductory section is followed by examples of the use of a Zeiss (Oberkochen) Planicomp C100 in analytical aerial triangulation, close range photogrammetry and the generation of digital height models. The examples demonstrate the suitability of the analytical plotter for numerical photogrammetry. Computer assistance and computer control allow for advanced data acquisition of high accuracy and speed. In addition, the minicomputer controlling the analytical plotter can be used for subsequent data processing. As a result, projects involving numerical photogrammetry can be carried out entirely in-house, without the need of an external computer.〈section xml:id="abs1-2"〉〈title type="main"〉RésuméLe restituteur analytique et la photogrammétrie numérique. On cite des applications du Planicomp C100: aérotriangulation analytique, photogrammétrie à courte distance, constitution de modéles numériques de terrain. Efficacité, rendement, haute exactitude, tels sont les avantages du restituteur analytique. On peut d'autre part bénéficier de l'ordinateur pour toutes sortes de traitements ultérieurs.〈section xml:id="abs1-3"〉〈title type="main"〉ZusammenfassungDer Beitrag beschäftigt sich mit dem Analytischen Plotter (AP) und seiner Auswirkung auf die Numerische Photogrammetrie. Nach einem kurzen Einführungsteil wird über den Einsatz eines Zeiss (Oberkochen) Planicomp C100 in der Analytischen Aerotriangulation, in der Nahbereichsphotogrammetrie und beim A ufbau Digitaler Höhenmodelle berichtet. Die Beispiele veranschaulichen die Eignung des AP für die numerische Photogrammetrie. Einerseits erlauben Rechnerstützung und Rechnersteuerung eine allgemeine, genaue und schnelle Datengewinnung. Darüberhinaus aber ermöglicht der, für die Steuerung des AP verfügbare Minicomputer die rechnerische Weiterverarbeitung der Messdaten. Auf diese Weise können numerisch-photogrammetrische Projekte ohne Einsatz eines externen Computers vollständig bearbeitet werden.

Notes: Book Reviewed in this article:SPHERE, SPHEROID AND PROJECTIONS FOR SURVEYORS. By J. E. Jackson.REMOTE SENSING IN ARCHAEOLOGY, CULTURAL RESOURCES TREATMENT AND ANTHROPOLOGY: THE UNITED STATES OF AMERICA IN 1979. By J. I. Ebert and T. R. Lyons.A HISTORY OF ARCHAEOLOGICAL AIR PHOTOGRAPHY IN GREAT BRITAIN. By R. R. Downey.PROCEEDINGS OF THE INDUSTRIAL AND ENGINEERING SURVEY CONFERENCE, LONDON, 1980. Edited by M. A. R. Cooper.ANALYSIS AND ADJUSTMENT OF SURVEY MEASUREMENTS. By E. M. Mikhail and G. Gracie.A HISTORY OF THE ORDNANCE SURVEY. Edited by W. A. Seymour.IN FOCUS: a rated guide to the best in photographic equipment. By J. Holtz.MAPS AND SURVEYS OF MALAWI. By C. G. C. Martin and other contributors.

Notes: When a member is thought to be domiciled or employed abroad, the name of the country has been added. Errors and omissions should be notified to the Honorary Secretary.

Notes: A brief review of work on airborne metric camera movement has been made. The tolerances for permissible image movement set by various investigators are discussed.The biggest single fault with most metric camera mountings in current use is that the centre of gravity of the camera is well above the line of action of the resilient elastic restoring forces. This results in coupling between the linear vibration of the airframe and the angular motion of the camera. There is a need for a simple device which can be attached to a survey camera in order to record angular motion during actual survey missions.〈section xml:id="abs1-2"〉〈title type="main"〉RésuméAprès une brève revue des travaux concernant les mouvements d'une chambre de prise de vue en vol, on discute les tolérances couramment admises pour ces mouvements.Le défaut de montage le plus fréquemment rencontré, est que le centre de gravité de la chambre est au-dessus de la ligne d'équilibre des forces agissantes.D'où un couplage entre la vibration longitudinale du porte-chambre et le mouvement angulaire de la chambre. Il faudrait créer un dispositif simple permettant d'enregistrer ce mouvement pendant les vols.〈section xml:id="abs1-3"〉〈title type="main"〉ZusammenfassungEs wird ein kurzer Überblick über die Arbeiten zur Bewegung von Luftbildmesskammern gegeben. Die von verschiedenen Autoren für die zulässige Bildwanderung angegebenen Toleranzen werden diskutiert. Der schwerwiegendste Fehler, der am meisten bei den gegenwärtig verwendeten Messkammern auftritt, ist der, dass der Kammerschwerpunkt über der Wirkungslinie der schwingungsdämpfenden Kräfte liegt. Daraus resultiert eine Paarung der linearen Vibration mit der Winkelbewegung der Kammer. Es besteht Bedarf für eine einfache Vorrichtung, die an einer Messkammer befestigt werden kann, um die Winkelbewegungen während des Bildflugs aufzuzeichnen.

Notes: . Micronuclear mitosis in living Spirostomum teres has been studied by sensitive polarization microscopy, and the dynamic aspects of micronuclear division are described. The small, spherical, interphase micronuclei lie in form-fitting depressions in the macronuclear surface. Nuclear division begins with the rounding and slight swelling of the macronucleus and, coincidentally, the micronuclei move out of the depressions and away from the macronucleus, increase in size, and become weakly birefringent. As mitosis proceeds, the micronuclei increase in uniaxial birefringence and elongate to form irregular ovoids that convert to angular structures displaying principal axes of positive birefringence so divergent as to appear oriented at a right angle to one another. Micronuclei maintain this appearance for as long as 60 min and then abruptly change to rectangular-shaped structures, increase in uniaxial birefringence, and begin anaphase elongation. The somewhat dumbbell-shaped micronuclei lengthen at the constant rate of 2.0 μm/min to reach lengths 〉70 μm. It appears that little half-spindle shortening occurs during spindle elongation. Accompanying the changes in micronuclear spindle length are changes in birefringence. Just before elongation begins, presumably metaphase, the micronucleus is uniformly and intensely birefringent. At the magnifications employed, a chromosome plate is not clearly visible as a region of reduced birefringence. As elongation begins, the putative half-spindles are more birefringent than is the interzone, a condition that is maintained until the spindles have achieved ∼30% elongation, at which time a region of increased birefringence develops at the center of the interzone. This pattern persists for a very short time, then gives way to a uniform birefringence of the entire separation spindle that is maintained until elongation is completed. The rate of micronuclear spindle elongation, changes in micronuclear dimensions, and corresponding changes in birefringence are discussed with respect to possible mechanisms of mitosis.

Notes: . Studies performed with the basidiomycete Laccaria trullisata collected from the sandy beach at the Hempstead Lake State Park, Long Island, New York, during the growing seasons of 1979 and 1980, have demonstrated a carposphere (equivalent to rhizosphere) effect. This region exerts a positive influence on the population density of amoebae when numbers are compared with those obtained in the bare sand 5 cm away. Moreover, amoebae have been shown to exist in, and have been recovered from, internal tissue of the cap (72%) and stalk (91%) of these mushrooms. A partial characterization of three strains of amoebae isolated from the internal tissue of L. trullisata and established in clonal culture is presented.

Notes: L'étude, par le protargol, des phénomènes infraciliaires et de leur corrélation avec les phénomènes nucléaires au cours de l'autogamie dans le genre Euplotes montre, par comparaison avec la conjugaison, que les diverses étapes de la morphogenèse sont liées à la progression de l'état nucléaire. Par ailleurs, l'étude comparative des différents types de morphogenèse (bipartition, phénomena sexuel, réorganisation induite par le jeǔne) permet de supposer qu'il existe deux territoires morphogènes soumis à des systèmes de régulation bien distincts. La comparaison des séquences de morphogenèse chez divers hypotriches conduit à dresser un plan général d'évolution de la régulation de l'activité corticale en relation avec l'étendue des remaniements associés à la stomatogenèse.〈section xml:id="abs1-2"〉〈title type="main"〉ABSTRACTThe changes in the arrangement of the infraciliature associated with autogamy in Euplotes are described and compared with similar events associated with conjugation. The successive steps of morphogenesis are strongly correlated with nuclear processes. The comparative study of different types of morphogenesis (binary fission, sexual phenomena, starvation-induced reorganization) leads to the hypothesis that two morphogenetic fields (a ventral one and a dorsal one) depend on separate regulatory systems. From the viewpoint of evolution, the morphogenetic sequences of some hypotrichs have been compared. A general scheme of the evolution of cortical regulation is proposed, taking into account the extension of the area concerned with stomatogenic activity.

Notes: Mouse omentum was studied after intraperitoneal challenge with tachyzoites of Toxoplasma gondii. Parasites inhabit omental histiocytes, fibroblasts, mesothelial cells, and free peritoneal macrophages. Recently infected cells showed enhanced metabolic and functional activity. Villous projections of the parasitophorous vacuole wall appeared, usually opposite the anterior pole of the parasite. In mesothelial cells, projections formed terminal swellings not observed in other infected cells. Activation of host cells was followed by reduction of the density of the cytoplasmic matrix, autophagosome formation, and intracellular edema, indicating the damage. The wall of the parasitophorous vacuole loses the supporting host cell endoplasmic reticulum that was attached to the vacuole just after entrance of the parasite into the cell. Then lysis of the parasitophorous vacuole and complete cell destruction occurs. The growth of parasites in undamaged cells does not coincide with the inflammatory response. Inflammation of the peritoneum develops only after the start of mass destruction of infected cells. Thus tachyzoites of Toxoplasma exert significant pathogenic effects by their ability to activate the host cell, causing lysis of the parasitophorous vacuole and subsequent destruction of the entire cell.

Notes: Discophrya collini is a free-living suctorian with retractile tentacles covered by a thick fibrous cortex. The tentacles contain a microtubular central canal surrounded at the base by a fibrous collar. Electrical stimulation induces a reproducible tentacle retraction. With extracellular electrodes, the tentacles nearest the anode respond initially, contracting by up to 75% of their original length. There is an inverse relationship between voltage level and duration of stimulus in producing a threshold response, and at a set voltage, between duration and degree of retraction. With intracellular electrodes, the membrane potential has been measured as -30 mV, and tentacle retraction occurs in response to as little as 1.25 nA when the intracellular electrode is made the cathode of the circuit. SEM studies show that retracted tentacles have a wrinkled cortex, while TEM shows that the microtubular canal bends as it enters the cytoplasm. No consistent changes occur in the microtubule configuration of the canal on retraction, suggesting that the microtubules are not directly involved in the contractile mechanism.

Notes: A rapid in vitro prescreen for Fe-binding chelators has been developed with growth of Crithidia fasciculata and the sparing of its heme requirement in a defined medium as a test system. The prescreen functions as an index of chelator-mediated Fe transport and as an index of growth inhibition, presumably by the interference with Fe and/or heme metabolism at intracellular chelatable sites. Of 161 chelators examined, 84 were active heme-sparers; 32 of these inhibited growth at low chelator concentrations. Twenty-eight other chelators inhibited growth and another 49 were inactive. Such chelating activity directed at Fe and heme targets in hemoflagellates may provide leads for chemotherapy.

Notes: Study of microorganism growth kinetics requires measurement of maximal specific growth rate. Standard methods of measurement-batch, semicontinuous and continuous steady state-have sources of imprecision that can be substantially reduced by a modification of the continuous steady-state method. Data are presented, using the ciliate Tetrahymena pyriformis, that indicate that the theoretical foundation of the new method is firm and that precision can be increased.

Notes: Viable merozoites of Plasmodium knowlesi were isolated and the proteins that were labeled on intact merozoites by lactoperoxidase-catalyzed radioiodination were identified. Sodium dodecyl sulfate polyacrylamide gel electrophoresis and autoradiography of Triton soluble extracts of labeled merozoites demonstrated eight major bands ranging in apparent molecular weight from 150,000 D to 22,000 D. Exposure of intact merozoites to trypsin (10 μg/ml) for 10 min resulted in the loss of the two highest molecular weight proteins (150,000 D and 105,000 D) and the appearance of two new bands at 70,000 D and 62,000 D. Trypsin treatment under these conditions also removed the receptor(s) for merozoite attachment to erythrocytes. Therefore, these high molecular weight proteins are candidates for the merozoite component that attaches to erythrocytes. There was no evidence that the labeled membrane components were serum or erythrocyte membrane components, two potential contaminants in the preparation. Anti-rhesus erythrocyte antibody did not precipitate labeled merozoite proteins. Furthermore, the immunoprecipitation of labeled merozoite proteins by rhesus anti-merozoite serum was not inhibited by erythrocyte ghosts.

Notes: Species of trypanosomatids without endosymbionts (Leptomonas seymouri, L. collosoma, L. samueli, Crithidia fasciculata, C. luciliae, C. acanthocephali, Herpetomonas megaseliae, H. mariadeanei, H. samuelpessoai, H. muscarum muscarum, Trypanosoma cruzi) and species of trypanosomatids with endosymbionts (Crithidia deanei, C. oncopelti, Blastocrithidia culicis) were comparatively studied by means of electron microscopy. Artificially aposymbiotic strains derived from species with symbiont were also included in the survey. Species with symbiont were found to differ in some ultrastructural aspects from the group of species without symbiont. Paraxial rods of flagella or intraflagellar structure were found exclusively in species without symbiont. Peripheral branching of mitochondria, accompanied by absence of subpellicular microtubules in sites where the mitochondrial branches are appressed to the cell membrane, were found exclusively in species with symbiont. Networks of kinetoplast DNA fibrils were found to be larger and looser in species with symbiont. Symbiont-free strains of species with symbiont retained the same morphological characteristics of their parental species.

Notes: During a freeze-fracture electron microscopical study of the plasma membrane of Tetrahymena, several different types of organized particle assemblies were observed. Three of these were found only on the protoplasmic face and were localized in the anterior-ventral region of the cell. These consisted of plate-like arrays composed of 4–25 triplet rows of small 3–4 nm particles; long, paired linear arrays localized at the tops of cortical ridges and composed of 7–8 nm particles; and elongated tetragonal arrays located in the grooves between ridges and composed of approximately 10 nm particles. The distribution of these arrays is consistent with roles in cellular morphogenesis, chemoreception, or cell-cell pairing during conjugation. In addition, a unique particle track associated with the cytoproct (anal pore) was observed in the external face of the plasma membrane. Furthermore, the protoplasmic face of the plasma membrane is characterized by a high density of particles organized into localized microarrays, consisting of small paracrystals or strings, which exhibit a loose higher-order patterning most evident toward the anterior end of the cell. Particle distributions on the protoplasmic face do not appear to be significantly altered by conditions that cause clumping of alveolar membrane particles. Taken together, these observations are consistent with the idea that the proteins of the plasma membrane are highly ordered and relatively immobile and that the structure of the plasma membrane is regionally differentiated.

Notes: . A new species of Dactylosoma (Dactylosomatidae, Piroplasmia), for which the name Dactylosoma hannesi n. sp. is proposed, was discovered in blood erythrocytes of Mugil cephalus, Liza richardsoni, and L. dumerili (Mugilidae) from Swartkops estuary, located east of Port Elizabeth, South Africa. The life cycle of this species differs in some respects from that described for all other known species of Dactylosoma and Babesiosoma. Mature schizonts contain eight nuclei but undergo division only to two to four daughter cells. During cytoplasmic cleavage, schizonts assume triad, rosette, or cruciform shapes. Merozoites are finally produced through a series of binary fissions of these daughter cells which may also be involved in additional nuclear divisions.

Notes: Electron microscopy was used to examine the flagellar apparatus of Herpetomonas ampelophilae from the gut and malpighian tubules of Drosophila melanogaster. The flagellates attach to the microvilli either by weaving their flagella between the microvilli or by engulfing several microvilli with an external flagellar membrane. The first type predominated in the gut while the second type was limited to the malpighian tubules. Desmosomes were not involved in either type of attachment. A subpellicular collar with emerging microtubules was found to be adjacent to the desmosome of the flagellar pocket of herpetomonads in the gut.

Notes: Prorocentrum micans Ehrenberg, a free-living marine dinoflagellate, was used to test the intracellular toxic action of cadmium. The cells were cultivated in Erdschreiber medium, with Cd concentrations of 10–100 ppb. Thin sections of treated cells, examined ultramicroscopically, exhibited vacuolations, increased numbers of lysosomes, and severe mitochondrial damage. The first two alterations are a general response to toxicity; the third is Cd specific. Although some chloroplasts were affected by Cd, they were not very sensitive to its action. The nuclear apparatus was not morphologically affected.

Notes: Toxoplasma-like avian parasites inhabiting mononuclear phagocytes have been called Haemogregarina, Toxoplasma. avian Toxoplasma, Atoxoplasma, and Lankesterella by various authors. My attempts to transmit the parasites by bloodsucking mites or by transfer of blood and tissues of infected sparrows and canaries were unsuccessful. However, it was noted that the infection was exacerbated under conditions that favored transmission of coccidiosis: crowding and lack of cleanliness. Oral inoculation of sporulated oocysts of Isospora resulted in death from overwhelming macrophage infection with Toxoplasma-like organisms. Experiments using sparrows and canaries showed that the Isospora species involved was not cross infectious. Further investigations using canaries demonstrated that after oral oocyst inoculation, infection of macrophages spread from the submucosa of the duodenum to the liver. spleen, and lungs. After several generations in the internal organs, asexual multiplication, occured in the intestinal epithelium of the small intestinc. Fecal oocysts first appeared at the end of 9–10 days. Oocysts continued to be passed in the feces for months after infection. This chronicity may be explained by the relatively long life of the macrophages that serve as host cells for the asexual stages as compared to the intestinal epithelium which is the cell type parasitized by conventional coccidia.

Notes: Stages of mitosis of the micronuclei of Stentor coeruleus were described as seen by transmission electron microscopy. Cells in division and those regenerating new oral membranelles were studied. Microtubules were found in early prophase in the karyoplasm and interspersed between the condensing chromatin. A monaxial intranuclear spindle is formed by early metaphase, with kinetochore microtubule attachment sites on the chromosomes. The spindle elongates, separating the daughter nuclei at anaphase. A new nuclear envelope, consisting of two unit membranes, begins to form at late anaphase. Small segments of membrane found in the space between the newly forming and the old micronuclear envelopes appear to fuse to form the new nuclear envelope. No ultrastructural differences were found in the mitotic nuclei of cells in division or regeneration.

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: . Strains of Tetrahymena thermophila were examined in an attempt to establish what role certain ions (Na+, K+, Li+, Ba++, Ca++, Mg++, Mn++, Al+++, Fe+++) play in influencing cell survival time in a culture medium. In short-term experiments (20–30 min), cell survival time in a 1% peptone medium is directly related to the valence of the ion employed. Long-term observations (lasting up to five days) in a 1% peptone medium containing lower ion concentrations revealed that the effects on cell-cycle time are not correlated with the valence state of the ion. Comparisons were made among the ionic resistances of strains of T. thermophila, of T. pyriformis sensu stricto, and of two subspecies of T. pigmentosa. Strains within a species are highly correlated in their patterns of ionic response, while marked differences between species occur. The most distinctive group of strains examined came from one of the subspecies (syngen 6) of T. pigmentosa.

Notes: . A two-stage chemostat modified to accommodate the growth of adhesive organisms was used to determine the yield constant, Y, of a representative soil amoeba, Acanthamoeba polyphaga, utilizing as its prey Pseudomonas paucimobilis. The first stage consisted of a glucose-limited bacterial culture in steady state. The second stage consisted of a simplified predator-prey system, nongrowing bacteria serving as the limiting substrate for amoebae. A refined methodology to more accurately determine Y was developed, and Y for Acanthamoeba polyphaga in batch and continuous culture was determined to be 19.1%.

Notes: . The swiftness of thermotaxis of Paramecium caudatum has been investigated for various populations of organisms by measuring the transient spatial distribution of the gathering process of organisms that are transferred to a temperature-gradient cell from the culture medium. The dispersion obtained from the spatial distribution for each population is found to decrease linearly with time and finally reach a steady state value. The gathering rate determined by the slope of the dispersion strongly depends on population; it increases with population.

Notes: . Blastocystis hominis, an anaerobic intestinal protozoan parasite of man, has a generation time (GT) in axenic culture of 8.5–19.4 h, depending on the strain tested. Average GT of the eight strains was 11.7 h. Zero growth time cell counts of 5.0 × 105/ml to 2.0 × 106/ml rose in 3–5 days to 1 × 107 or 1 × 108 cells/ml. The GT was determined for the 24-h period during which the most rapid growth occurred; about 2% of the B. hominis cells were in division during this time. Division under the culture conditions provided was by binary fission, the usual mode for B. hominis in vitro as well as in vivo. Division times were determined also by direct observation of individual dividing cells in slide cultures. These were usually ca. 40–60 min but sometimes as low as 20 min.

Notes: In contrast to the situation in 13 other species of the Tetrahymena pyriformis complex, in which the condensed degenerating old macronucleus lies in the posterior end of the cell during the late stages of conjugation, in Tetrahymena tropicalis that nucleus is found in the anterior portion. This developmental characteristic may be useful for taxonomic purposes as well as being of value in investigations on nucleocytoplasmic interaction.

Notes: Eimeria nuttalli oocysts were found in 58% (21/36) and E. procyonis oocysts in 25% (9/36) of raccoons Procyon lotor in Illinois, and sporocysts of Sarcocystis sp. in 17% (2/12) of other raccoons in Illinois. The oocysts of E. nuttalli were ellipsoidal to ovoid. 15–21 × 12–17 μm, with a one-layered, smooth, colorless wall. The oocysts of E. procyonis were 22–28 × 18–22 μm, with a rough, striated, brownish, two-layered wall. The sporulated sporocysts of Sarcocystis sp. were 11–13 × 8–10 μm. Attempts to infect baby pigs by feeding them sporocysts of Sarcocystis sp. from the raccoon failed.

Notes: Comments are made concerning the work reported at this Conference by Dr. Edith Box. The importance of stress on the animals used in experimental work is emphasized. Difficulties in identification of isosporan species in birds are mentioned.

Notes: A trypanosomatid flagellate, Leptomonas sp., develops and multiplies in the macronucleus (only) of natural and laboratory-reared populations of the ciliate Euplotes. Up to 90% of the natural populations of Euplotes in our test pond had such nuclear infections. Laboratory infections were transmitted to this ciliate by feeding it liberated parasites. Paramecium resisted infections. All laboratory-induced infections were lethal to Euplotes, while control clones of the uninfected ciliates remained viable. This leptomonad, unlike Leptomonas karyophilus (found in Paramecium), shows no leishmanial forms in its several ciliate hosts and shows a varied pattern of locomotion.

Notes: Some generalizations of a decade ago are reexamined in light of modern advances in coccidiology. Perhaps surprisingly, not many modifications need or can yet be made. Future successes of significance will be in areas of immunology and chemical genetics.

Notes: Stocks of the Tetrahymena pyriformis complex have been collected in North America and their mating reactivity has been studied. In addition to stocks mating with Tetrahymena americanis, T. borealis, T. pigmentosa, T. hyperangularis, and T. australis, stocks belonging to old syngen 5 and three new mating groups, numbers 13, 14, and 15, were discovered. Syngen 5 and groups 13 and 14 are distinct “biological” species, based on their reproductive isolation from other groups and on the ability of withingroup crosses to produce immature progeny. These species have been named T. hegewischi n. sp., T. sonneborni n. sp., and T. nipissingi n. sp., respectively. The cross between the two group 15 stocks did not produce immature progeny, and there is not sufficient evidence to conclude that this pair of stocks represents a separate species. Temperature tolerance measurements have been made on stocks representing all known micronucleate members of “pyriformis” complex. Within each species, the range of temperature tolerances is narrow; the average within-species standard deviation is 0.63°C. The species averages range from 32.7 to 40.7°C. Using syngen numbers, the order from lowest to highest temperature tolerance is 9, 8, 10, 7, 6, 4, 13, 14, 12, 11, 5, 3, 2, 1. The large differences among species make temperature tolerance a useful aid in identification, but the origins of the differences among species are unknown.

Notes: Members of the family Sarcocystidae, as defined by Frenkel, have had a complicated history, principally due to the existence of both coccidial and cystic stages. This formerly clandestine relationship resulted in dual or partial designations of nomenclature for individual species. The problem was further compounded by the obligatory heteroxeny of several of the genera, making it impossible to transmit the parasites from one individual to another of a single host. As a result, oocysts similar in appearance, though from hosts separated taxonomically up to the familial level, were sometimes considered to be identical. Discoveries within the last decade have generated much interest and some understanding. Current studies of these and other coccidia should emphasize complete cyclical transmissions with cognizance of potential heteroxeny with the production of tissue cysts in intermediate hosts.

Notes: Book reviews in this article: Ecology and Parasitology. Alexander, M., ed. 1980. Advances in Microbial Ecology Smith, H. G. 1978. The Distribution and Ecology of Terrestrial Protozoa of Sub-Antarctic and Maritime Antarctic Islands Taylor, Angela E. R. & Muller, R., eds. 1980. Vaccines Against Parasites Kreier, Julius P., ed. 1980. Malaria New Textbook of Protozoology Farmer, John N. 1980. The Protozoa: Introduction to Protozoology Phytoflagellates and Serial Endosymbiosis Theory Cox, Elenor R., ed. Phytoflagellates Tappan, Helen. 1980. The Paleobiology of Plant Protists. Margulis, Lynn. 1981. Symbiosis in Cell Evolution: Life and Its Environment on the Early Earth. Intercellular Communication and Nuclear-Cytoplasmic Interactions O'Day, Danton H. & Horgen, Paul A., eds. 1981. Sexual Interactions in Eukaryotic Microbes Whitson, Gary L., ed. 1980. Nuclear-Cytoplasmic Interactions in the Cell Cycle. Invertebrate Texts Alexander, R. McNeill. 1979. The Invertebrates Barnes, Robert D. 1980. Invertebrate Zoology Engemann, Joseph G. & (the late) Hegner, Robert W. 1981 Invertebrate Zoology ATCC Catalogue of Strains Hatt, Harold D., ed. 1980. The American Type Culture Collection: Catalogue of Strains I.

Notes: Polyamines are multiply amine-substituted straight-chain aliphatics; their content in different tissues may vary widely, and their functions are many. Their main routes of biosynthesis originate from ornithine and methionine. Polyamine content and biosynthesis in tryposomatid flagellates are reviewed concluding with emphasis on their possible role as critical drug targets in these parasitic protozoa so pathogenic for man in large areas of the world.

Notes: During spring and autumn, the total number of amoebae and the number of Acanthamoeba species able to grow at 37°C were determined in six thermally polluted factory discharges and the surrounding surface waters. The isolated Acanthamoeba strains were studied for growth in axenic medium, cytopathic effect in Vero cell cultures, and virulence in mice. Although more amoebae were isolated in autumn, the number of Acanthamoeba species was lower than in spring, when the percent of pathogenic strains among the isolates was highest. Higher concentrations of amoebae were found in warm discharges, and more virulent strains occurred in thermal discharges than in surface waters.

Notes: Eight species of loricate choanoflagellates (Acanthoecidae), Acanthoecopsis spiculifera Norris, Bicosta antennigera Moestrup, Bicosta spinifera Throndsen, Calliacantha multispina Manton & Oates, Calliacantha simplex Manton & Oates, Crinolina aperta Leadbeater, Diaphanoeca multiannulata n. sp., and Parvicorbicula socialis (Meunier) Deflandre, have been observed, by light and electron microscopy, in samples obtained from the Weddell Sea during the austral summer of 1977. Diaphanoeca multiannulata is described for the first time from these samples: the other organisms are discussed. The distribution of most species within the Weddell Sea was widespread. Habitats in which choanoflagellates were found included the water column, the edge of (or ponds on) ice floes, and the interior of ice floes. The distributional, environmental, habitat, and/or morphological range of all previously described species is expanded. Methods of variation of transverse costal diameters between genera may be potentially useful to the understanding of taxonomy and phylogeny of this family.

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: . Allantosoma intestinalis, a suctorian ciliate isolated from the intestine of the horse, was studied utilizing light and electron optical methods. These small sausage-shaped organisms have a varying number of tentacles (between one and 12) located at each extremity of the body. The microtubular axoneme of each tentacle in cross-section consists of two files of microtubules arranged in a daisy-like configuration. Haptocysts occur in the tentacle shaft, abutted to the plasma membrane of the knob of the tentacle, and in the cell body. The haptocysts are bottle-shaped, with prominent annular striations around their midportion. The cell is covered by three membranes, an outer plasma membrane, an outer alveolar, and an inner alveolar membrane. A thin epiplasmic layer is found beneath the inner alveolar membrane, and a single row of microtubules underlies the epiplasm. The subpellicular microtubules are arranged parallel to each other forming a corset around the cell along the long axis: such a system is not characteristic of suctorians. A field of diminutive kinetosomes (each 180 nm long, max. of 15 per field), lacking cilia, was found below the cortex. The function of these prokinetosomes is unknown. A ciliated swarmer has not been observed, only the nonciliated adult. The characteristics of Allantosoma are compared with those of other suctorian genera.

Notes: . Temperature shifts have been used to block critical points in the conjugation sequence of Paramecium tetraurelia. Increasing temperatures above 27°C reduced ciliary agglutination, pair formation, and nuclear exchange; a complete inhibition of these stages occurred at 37°C. Temperatures below 19°C had no effect on ciliary agglutination or nuclear exchange but completely inhibited pair formation. The bases for the cells’ inability to form pairs at 19°C and 37°C were sought. Cells placed below 19°C were unable to deciliate or fuse membranes in the holdfast region; at 37°C, membrane fusion in both the holdfast and paroral regions was prevented. Time course studies on cross-fertilization reveal that temperatures 35°C block all stages of the process up to the actual exchange of pronuclei. After the exchange has begun, the process continues despite the elevated temperature. Temperature shifts are discussed as a means of conditionally blocking critical points in the developmental program of conjugation.

Notes: . [14C]chimyl and [3H]batyl alcohols were added to Crithidia fasciculata cultures during the mid-log phase of cell growth, and the lipid extracts of the cells were analyzed for degradation products. C. fasciculata cells were able to take up exogenous glyceryl ethers, and in amounts as high as the endogenous lipid content. The glyceryl ether taken up by the cells was incorporated into lipids either prior to the ether bond cleavage or after degradation to fatty acid. The extent of degradation and the degree of incorporation of degradation products into cellular lipid were higher for chimyl than for batyl alcohol. Batyl alcohol was not metabolized efficiently, leading to the formation of large intracellular pools of free substrate. One product of glyceryl ether degradation was identified as alkyl-dihydroxy acetone, and was detected inside and outside of the cells. The data strongly suggest that this product is the first stable intermediate in the degradation process and indicate that the extracellular formation of alkyl-dihydroxy acetone is due to the action of exocnzyme; ecteted by the cells. The constant detection of alk I cnyl glycerol among the degradation products indicates the existence of a second mechantsm in C. fasciculata for converting the alkyl-to alkenyl-glycerol.

Notes: . Sick budgerigars from a local aviary were found to be infected with Giardia. The trophozoites were of the Giardia duodenalis type as defined by Filice with elongate median bodies pointed on one or both ends and more or less perpendicular to the long axis of the body. Using three fixation-staining methods, and material from three birds, the length ranged from 10 to 18 μm and the width from 4.5 to 11 μm with a mean length to width ratio of 2. Attempts to culture the trophozoites in vitro from intestinal scrapings were unsuccessful. Also attempts to transmit the infection by fecal cysts to canaries and mice failed. It is proposed that the budgerigar form be called Giardia duodenalis, race psittaci.

Notes: Three species of Pseudocohnilembus were examined with respect to infraciliature and the silverline system. The freshwater species P. putrinus and P. pusillus exhibited no differences in general organization of the argyrophilic structures when compared with the marine P. marinus. A review of the Pseudocohnilembus species that have been described on the basis of silver preparations shows that at present four species have been well characterized: P. pusillus (Quennerstedt, 1869) nov. comb., P. putrinus (Kahl, 1928) nov. comb., P. hargisi Evans & Thompson, 1964, and P. marinus Thompson, 1966, P. persalinus Evans & Thompson, 1964 and P. longiseta Evans & Thompson, 1964 are regarded as identical with the older known P. pusillus, because with respect to morphology and argyrophilic structures they are within the range of variability of that species; and their names thus fall as synonyms of P. pusillus.

Notes: The structure of micronemata arising from the surface of the bloodstream form of Trypanosoma gambiense was studied by electron microscopy. In order to produce micronemata, trypanosomes were incubated in either 1) phosphate buffered saline supplemented with glucose (PBSG), 2) immune mouse serum or 3) PBSG after passage through a DEAE-cellulose column. Electron microscopic examination of the parasite revealed the presence of thread-like micronemata arising from the anterior end and from the flagellar pocket regardless of the incubation conditions. Negative staining revealed a distinct peripheral fringe layer with nodular protrusions covering the entire surface of the micronema. The distribution and number of intramembrane particles (IMP) on the P and E faces of the micronema were similar to those of the flagellum of T. gambiense, indicating a close relationship between the membrane structure of the micronema and the flagellum. Micronemata became fragmented and adhered to each other after incubation of the parasite in the media for 12 h. Since micronemata tend to have the characteristics of adhesiveness and fragmentation, fragments of these structures might adhere to various host organs. Dispersal of potential antigenic material might be responsible, in part, for the induction of the host immune response.

Notes: The motion of Paramecium caudatum has been investigated at various temperatures by measuring the transient behavior of spatial distribution in the diffusion process of organisms that, by electric stimulus, are initially gathered at a single place in the glass culture cell. The spatial distribution through the course of diffusion has a nearly Gaussian profile. Dispersion was obtained at 1 sec intervals and increased linearly with time. The time dependence of the dispersion gave a diffusion coefficient for the random motion of the organisms. The results show that the diffusion coefficient has a maximum at the temperature at which the paramecia were cultivated.

Notes: . Conjugating cells of Euplotes vannus (syngens Naples and Barcarès) were investigated for Con A-binding sites by means of fluorescence microscopy. Cells fixed with 0.4% paraformaldehyde and incubated with 15 μg/ml FITC-Con A showed a distinct region of strong fluorescence, the size, shape and localization of which characteristically changed during the course of conjugation, first appearing at courtship stage (cells contact without forming pairs) and vanishing soon after the migration pronuclei have been exchanged, but before cells have separated. Con A binding and conjugation were blocked by cyclohexamide and α-galactosidase. Con A-binding was also inhibited by α-mannosidase, α-glucosidase and β-galactosidase without affecting conjugation except a delay of pair formation. The results suggest an involvement of newly formed or translocated glycoconjugates in cell pairing during conjugation.

Notes: . The development of Sarcocystis cruzi was studied in an 11-day-old calf killed seven days postinoculation with 5 × 108 sporocysts from feces of coyotes. Uninucleate zoites were found in arteries of mesenteric lymph nodes but not in other organs. Zoites measured 4.9 × 3.0 (3.5–7.0 × 2.1–3.5) μm. Of the 36 zoites studied, 31 were in endothelial cells, four were in macrophages in the lumen of arteries, and one was free in the lumen of an artery. Infected endothelial cells were two to three times larger than uninfected cells. Zoites appeared structurally similar to sporozoites. The occurrence of zoites in macrophages suggests that sporozoites of Sarcocystis might use such cells to reach the site of their first merogony.

Notes: . The enzyme that catalyzes the critical conversion of the proposed reductive thymidine catabolic end product, P-aminoisobutyric acid, to the initial anabolic reutilization substrate, probably methylmalonic semialdehyde, was investigated to un- ambiguously substantiate the operation of a reductive pyrimidine catabolic and reutilization pathway in Tetrahymena pyriformis strain GL. Although most of the studies on the further metabolism of P-aminoisobutyric acid in other organisms suggested transamination of p-aminoisobutyric acid to methylmalonic semialdehyde followed by its further oxidation to methylmalonic acid, such a transaminating system could not be demonstrated. By means of a sensitive fluorometric assay system, however, a low, but significant amount of P-aminoisobutyric acid oxidase activity was detected. This enzymatic activity exhibited the following characteristics in homogenates: good activity in alkaline 0.2 M Tris-HCI buffer with a rather broad pH optimum ranging from 7.8 to 9.0; optimum activity at a temperature of 37°C; stimulation on the addition of exogenous FAD; inhibition on the addition of divalent cations, EDTA, or PCMB; little stimulation on the addition of detergents; and no increase in activity on repeated freezing and thawing. In addition, crude preparations of this oxidase were found to be relatively stable when stored up to one week either refrigerated or frozen, to have a specific activity of 2.8 nmoles/min/mg of protein, and to have a K, of 3.6 × 10− M for d,l-β-aminoisobutyric acid. Whether this high Km, is physiologically significant or not, however, will have to await further investigation. Preliminary (NH4)2SO4 fractionation and affinity chromatography studies also indicated that this enzyme appears to be a unique and specific oxidase whose activity is separable from other marker enzymes, including other oxidases.

Notes: . Phosphatase activity in Trypanosoma rhodesiense has been examined histochemically by light and electron microscopy and by enzymatic assay in homogenate fractions. Using a method with lead as capture ion, acid phosphatase was found in lysosome-like vesicles and in the flagellar pocket. No alkaline adenosine triphosphatase (ATPase) was detectable by this method. Direct assay of p-nitrophenylphosphatase activity in homogenate fractions showed that acid phosphatase activity was strongly membrane-bound, but that activity at pH 9 was minimal in both soluble and particulate fractions. “Endogenous” ATPase activity was localized specifically and reproducibly in the mitochondrial membranes and under the plasma membrane of the flagellum. This nonenzymic reaction product could not be eradicated by glycerol extraction or glucose depletion. Unlike the membrane staining, which was manifest only after lead treatment, heat-resistant electron-dense material was found in the matrix of lysosomal vesicles in trypanosomes fixed in glutaraldehyde only and not subjected to further treatment with heavy metal reagents. X-ray emission analysis showed the presence of calcium and phosphorus, indicating that the matrix might have a phosphate storage function.

Notes: The longitudinal flagellum of Ceratium tripos moves in two dissimilar ways: undulation and retraction. The undulatory wave is planar and has a wavelength of 74.3 ± 9.6 μm and an amplitude of 14.2 ± 2.3 μm in sea water. The beat frequency is 30 Hz at 20°C, pH 8.0. The retractile motion is unique to Ceratium and is triggered by mechanical stimulation on the cell body, especially at the tip of the apical horn. When it retracts, the longitudinal flagellum folds every 4–5 μm along the flagellum. Cinematographic study showed that the flagellum folded from tip to base and was finally installed into the sulcus, a groove on the ventral side of the cell. This motion is completed in sea water within 28 msec. The retracted flagellum then re-extends and restores the undulation within a few seconds. The flagellum unfolds in the proximal portion first, then the distal, and finally the middle portion. Fixation always triggers the retraction. Scanning electron microscopy showed that the flagellum is folded and secondarily twisted in a helix. A new fiber in addition to the flagellar axoneme was found in the retracted flagellum by phase microscopy. This fiber (R-fiber) seems to contract during the retraction to fold the flagellum.

Notes: Phagocytosis of culture forms of Trypanosoma cruzi was assayed by a radioisotopic method. Purified polymorphonuclear leukocytes (PMN) were mixed with 3H-uridine-labeled T. cruzi epimastigotes in the presence or absence of anti-T. cruzi antibodies. The reaction was stopped by adding N-ethyl-maleimide, and noningested parasites were lysed by complement. The percentage of radioactivity incorporated into the PMN pellet was recorded. The phagocytosis reaction was rapid, yielding maximum incorporation at 30 min at which point the radioactivity associated with the PMN cells decreased through release of the isotope to the supernatant. The degree of incorporation of radio-labeled parasites was a function of the effector/target cell ratio and the antibody concentration. The method is suitable for the quantitative determination of phagocytosis of T. cruzi by normal PMN.

Notes: The following species of the gregarine genus Lankesteria were found in a study of ascidians from Monterey Bay, on the central California coast of the Pacific Ocean: L. abbotti n. sp. in Clavelina huntsmani, L. aplidii n. sp. in Aplidium solidum, L. ascidiae in Ciona intestinalis, L. diaphanis n. sp. in Archidistoma diaphanes, L. euherdmaniae n. sp. in Euherdmania claviformis, L. montereyensis n. sp. in Archidistoma molle, L. pescaderoensis n. sp. in Ritterella rubra, L. pittendrighi n. sp. in Ascidia ceratodes, L. psammii n. sp. in Archidistoma psammion, L. ritterellae n. sp. in Ritterella pulchra, L. ritterii n. sp. in Archidistoma ritteri, L. synoici n. sp. in Synoicum parfustis, and Lankesteria sp. in Botrylloides sp. No gregarines were seen in the following ascidians: Aplidium californicum, A. propinquum, Botryllus tuberatus, Diplosoma macdonaldi, Perophora annectens, and Polyclinum planum.

Notes: The effect of holothurin (a marine biotoxin) on the resistance of mice to Trypanosoma musculi was measured by studying changes in the parasite population in vivo. Swiss Webster (SW), Beige (BG), and Black (BL) mice treated with holothurin prior to and simultaneously with infection of trypanosomes had lower parasitemias than controls. Higher levels of parasitemia were observed in mice treated after infection with trypanosomes. The timing of administration of holothurin appeared to be an important factor in the observed effect. The minor variations in the parasitemia seemed to be related to the mouse strain.

Notes: The structure of the cyst wall of the heliozoon Echinosphaerium nucleofilum has been investigated using light microscopy, scanning and transmission electron microscopy, and X-ray microanalysis. The cyst wall is a composite structure of seven or eight layers. These are: an enveloping gelatinous layer; a layer of siliceous spheroidal bodies; an electron-dense supporting membrane; a broad electron-lucent zone; an electron-dense layer; a layer of helicoidally packed material; and one or two layers with a granular appearance lying next to the plasma membrane of the encysted organism. The structure of the cyst wall closely resembles that of Actinophrys sol, confirming the close relationship of these actinophryid heliozoa while emphasizing their distinctiveness from other amoeboid protista.

Notes: Morphogenesis of cell division was investigated in Diophrys scutum, D. oligothrix, and D. appendiculata utilizing both light microscopy of living and stained specimens and SEM of preserved specimens. The cortical morphogenetic pattern of Diophrys is similar to that of other members of the family Euplotidae. The opisthe oral primordium, which develops in a subsurface pouch, forms posterior to the parental buccal cavity. The proter inherits the parental adoral zone of membranelles (AZM) apparently unchanged. The endoral membrane forms to the right of the posterior end of the AZM in the proter, in association with the developing AZM in the opisthe. The paroral cirrus and membrane develop from a single streak that first appears along the right edge of the buccal cavity in the proter to the right of the developing buccal structures of the opisthe. Frontal and transverse cirri develop in both proter and opisthe from five separate cirral primordia that form to the right of the buccal cavity. Left marginal cirri do not develop in association with the corresponding parental structures. Kinetosomes formed within the opisthe oral primordium, or kinetosomes that were part of any parental ciliary structure, do not appear to become part of any developing paroral structures, frontal, transverse, or left marginal cirri. Speciation within the genus Diophrys and evolution of the family Euplotidae as they relate to the morphogenesis of cortical structure are discussed.

Notes: Autecology (cellular organelles and secretions, encystment and dispersal abilities), environmental conditions (physiological tolerances and interaction with other organisms), and evolutionary history contribute to protist biogeography, which manifests ecological and historical aspects. Ecological biogeography is seen in the influence of geochemistry on the distribution of fresh-water phytoflagellates and algae, and of moisture and vegetation type on soil-litter protists. A temporal feature is often present because many protists encyst and respond only to certain ranges of temperature and organic content. Historical biogeography has occurred by radiative host evolution on symbiotic protozoa (e.g., termite flagellates and rumen ciliates), and by the isolating effects of water currents, temperature, and density gradients on oceanic protists (coccoliths, dinoflagellates, foraminifera, radiolaria, and tintinnines). These two aspects combine in protists living on animal surfaces. Humans affect protist biogeography by increasing parasite ranges through human migrations and by water pollution. They can diminish these situations by disease control and exploiting appropriate ciliates in sewage disposal. Many free-living protozoa appear to be cosmopolitan, but mating types and isoenzyme studies suggest that speciation with its geographic connotations may be more widespread than presently appreciated.

Notes: Available evidence indicates that many of the antiprotozoal drugs currently in use significantly modify the immune response of the host. The effect depends on both the drug and the host. Some drugs enhance the immune response, some are immuno-suppressants, and others enhance some types of immune mechanisms while suppressing others. Future efforts in the development of antiprotozoal drugs should consider their effects on both the parasite and the immune response of the host. Also in the chemotherapy of protozoal infections consideration should be given to the combined usage of immunoenhancing agents and antiprotozoal drugs.

Notes: A survey of protozoa polluting bottled mineral water in Mexico was carried out using samples obtained from the three best-selling brands of bottled mineral water in the country. The organisms were concentrated through filtration procedures and subsequently cultured in sterile media. The cultures were observed over four weeks, with identification to the level of genus and species. Most commonly found were the amoebae Naegleria gruberi, Acanthamoeba astronyxis, and Vahlkampfia vahlkampfi (trophic as well as cystic stages) plus one flagellate, Bodomorpha minima. No ciliates were detected. The public health importance of the findings is obvious, since some strains of Naegleria and Acanthamoeba have the potential to cause human disease that may lead to death.

Notes: . Amphidinium carteri was unable to grow on nutrient-enriched seawater in the presence of 200 μg/ml fluoride (F) but could be adapted to grow successfully on this F concentration when repeatedly cultured with stepwise increases in sub-inhibitory F concentration. Electron microscopic investigation of the F-adapted dinoflagellate cells showed abnormal ultrastructural features in the chloroplast (especially the pyrenoid), mitochondria, and nucleus. Simultaneous comparison with the F-inhibited dinoflagellate cells showed that thylakoid formation was extremely disorganized by fluoride and that F-adaptation conferred a prolamellar-like configuration on the thylakoids in the center of the pyrenoid. This unexpected appearance of lamellae formation in the F-adapted cells suggested that the pyrenoid may be a center for thylakoid assembly. Such cells also showed large, intensely osmiophilic inclusions in the mitochondria. Microbodies are found in close juxtaposition to the mitochondria and chloroplast, suggesting an increased metabolic dependence on photorespiration. The F-adapted nucleus showed dark and light concentric rings in the nucleolus region, accompanied by other signs of mitotic activity, which were not observed in the F-inhibited cells. It was inferred that the F-adaptation may have required some form of genetic change resulting presumably in the development of a phenotype mutant.

Notes: . The large fresh-water microaerobic amoeba Pelomyxa palustris does not contain mitochondria, but three types of bacterial endosymbionts are always present. Thus, it is of interest in the discussion of the possible origin of mitochondria from primitive prokaryotes. Gas exchanges (O2, CO2) and concentration of endosymbionts were determined in individual amoebae, in which the life cycle stage was noted. Grey type (stationary phase) amoebae had a lower O2 uptake and lower endosymbiont concentration than light type (growth phase) amoebae, and highest O2 uptake was found in centrifugal pieces of light type Pelomyxa, centrifuged in vivo, which contained nearly all of the endosymbionts. In light type amoebae, the respiratory activity was independent of O2 concentration between 1 and 21%, and, when compared on the basis of dry weight and protein, of the same order as that of other free-living protozoa. The R.Q. was slightly higher than 1, indicating that glycolysis does not play a significant role in energy metabolism. It is concluded that P. palustris is fully aerobic, and suggestions are presented as to the role of the endosymbionts in its respiratory metabolism.

Notes: . A series of new in vitro systems for the cultivation of bloodstream forms of Trypanosoma (Trypanozoon) brucei brucei, T. (T.) b. rhodesiense, and T. (T.) b. gambiense was developed. The standard system consists of a feeder layer of fibroblast-like cells derived from embryos of New Zealand White rabbits (REF) or a mountain vole, Microtus montanus (MEF), with HEPES-buffered Minimum Essential Medium (MEM), with Earle's salts, supplemented with 15% inactivated rabbit serum. These two and other feeder layers were cross-checked with different sera to test for growth support of bloodstream forms of the three trypanosome subspecies studied. Cultures could be initiated with bloodstream forms from mammalian hosts or from cryopreserved stabilates. Metacyclic forms from infected Glossina m. morsitans could also be used as inoculum; they transformed within 6 h to bloodstream forms. Maintenance of cultures and growth properties are described in detail. Experiments were undertaken to confirm that the cultivated bloodstream forms still possess some of the characteristic features of pleomorphic bloodstream populations. Cultivated bloodstream forms were always infective for mice, and a surface coat could be demonstrated by electron microscopy. They could also be cyclically transmitted through tsetse flies, and the metacyclic forms from these flies could be brought back into culture. In vitro cloning with single bloodstream forms and metacyclic forms could be achieved with high cloning efficiency. The consumption of glucose and the production of pyruvate and lactate were determined.