ALBERT

Notes: The author has been involved in the manufacture of photogrammetric instruments for nearly 30 years. In particular, he was associated with the Thompson-Watts plotter and, at the present time, is concerned with the production of the CP1 and EMPD instruments which owe a great deal to his design and innovatory skills. This paper summarises his experiences and views of the production of photogrammetric equipment in England.〈section xml:id="abs1-2"〉〈title type="main"〉RésuméPendant 30 ans l'auteur a participéà l'élaboration d'appareillages pour la photogrammétrie: en particulier les restituteurs Thompson–Watts; et maintenant les appareils CP1 et EMPD qui lui doivent beaucoup. Il condense ici l'expérience et les idées qu'il a dans ce domaine.〈section xml:id="abs1-3"〉〈title type="main"〉ZusammenfassungDer Autor ist seit fast 30 Jahren an der Herstellung photogrammetrischer Auswertegeräte beteiligt. Insbesondere verbunden war er mit dem Thompson–Watts Plotter und befasst sich gegenwärtig mit der Fertigung der Geräte CP1 und EMPD, an denen er durch seine schöpferischen Fähigkeiten grossen Anteil hat. In dem Artikel werden seine Erfahrungen und Ansichten bei der Produktion photogrammetrischer Geräte in England zusammengefasst.

Notes: An application of photogrammetry in the measurement of palatal surface area is described. The accuracy of the photogrammetric method in such applications is also discussed.〈section xml:id="abs1-2"〉〈title type="main"〉RésuméDétermination par photogrammétrie de l'aire du palais buccal; indications sur l'exactitude obtenue.〈section xml:id="abs1-3"〉〈title type="main"〉ZusammenfassungDie Anwendung der Photogrammetrie zur Vermessung der Gaumen-oberfläche wird beschrieben und die Genauigkeit photogrammetrischer Verfahren bei solchen Messungen werden diskutiert.

Notes: A camera calibration method for object distances of 1 m to 4 m is described.〈section xml:id="abs1-2"〉〈title type="main"〉RésuméOn décrit une méthode d'étalonnage de chambres de prise de vues pour des distances de prises de vues de 1 à 4 mètres.〈section xml:id="abs1-3"〉〈title type="main"〉ZusammenfassungDiskussion eines Verfahrens zur Kammerkalibrierung für Aufnahmeentfernungen von 1 m bis 4 m.

Notes: Stereophotography with a pair of 35 mm cameras and stroboscopic illumination was used to record, reconstruct and measure the trajectories of falling hailstones under extremely adverse natural conditions. Since it was not possible either to fix or to measure precisely the camera positions and orientations, a method was devised to obtain both the three dimensional hailstone co-ordinates and the camera positions and orientations by making use of the otherwise redundant information contained in the stereo-photography.〈section xml:id="abs1-2"〉〈title type="main"〉RésuméOn a utilisé deux cameras de 35 mm et un éclairage stroboscopique pour enregistrer en vue de leurs restitutions les trajectoires de grêlons; ceci n'a pu être réalisé que dans des conditions difficiles. Comme il n'était pas possible de stabiliser les cameras et de déterminer les coordonnées des points de station, on a mis au point une méthode spéciale.〈section xml:id="abs1-3"〉〈title type="main"〉ZusammenfassungDie Stereophotographie mit einem Paar von 35 mm Kameras und stroboskopischer Beleuchtung wurde angewendet, um die Kurven fallender Hagelkörner unter extrem von den natürlichen abweichenden Bedingungen zu registrieren, rekonstruieren und zu vermessen. Da es nicht möglich war, die Kammerstandpunkte und -orientierungen zu fixieren oder exakt zu vermessen, wurde ein Verfahren abgeleitet, um sowohl die dreidimensionalen Koordinaten der Hagelkörner als auch die Kammerparameter durch Verwendung der durch die Stereophotos gelieferten redundanten Informationen zu erhalten.

Notes: The Ordnance Survey's approach to the revision of the 1: 2500 scale series is discussed, with particular emphasis on the variety of photogrammetric methods which are used. The special problems of re-casting existing maps onto the National Grid projection, without losing the value of the existing detail, are outlined whilst emphasising the need to complete the revision with maximum speed to an adequate accuracy for a minimum cost.〈section xml:id="abs1-2"〉〈title type="main"〉Résumé On expose les méthodes de l′ Ordnance Survey en matière de révision des levés au 1: 2500; on examine le problème de l'adaptation des levés existants au système cartographique national, sans qu'il y ait perte de richesse.〈section xml:id="abs1-3"〉〈title type="main"〉Zusammenfassung Es wird ein Versuch des Ordnance Survey zur Laufendhaltung der Karte 1: 2500 beschrieben, wobei die verschiedenen photogrammetrischen Verfahren, die angewendet wurden, besonders betont werden. Die speziellen Probleme der Einpassung bestehender Karten in das Nationale Gitternetz ohne den Verlust der vorhandenen Details werden skizziert, wobei hervorgehoben wird, dass die Revision mit maximaler Geschwindigkeit ohne Genauigkeitsverlust bei minimalen Kosten durchgeführt werden muss.

Notes: Microrelief mapping of the sea bed can only be carried out by photo-optical methods. It is shown that suitable equipment, bought off the shelf, can produce useful results. The paper describes equipment performance trials and a practical application in a study of large scale sea bed topography.〈section xml:id="abs1-2"〉〈title type="main"〉RésuméLa cartographie du microrelief de fonds sous-marins ne peut être faite qu'à partir de photos. On montre, qu'avec un appareillage convenable on peut obtenir des résultats intéressants. On décrit les tests, ainsi qu'un travail pratique d'application à un levéà grande échelle de fonds sous-marin.〈section xml:id="abs1-3"〉〈title type="main"〉ZusammenfassungDie kartographische Darstellung des Mikroreliefs des Meeresbodens kann nur auf photo-optischem Wege durchgeführt werden. Es wird gezeigt, dass mit einer geeigneten Ausrüstung günstige Ergebnisse erzielt werden können. Im Artikel werden Versuche zur Testung der Ausrüstung und eine praktische Anwendung zum Studium einer grossmassstäbigen Meerestopographie beschrieben.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

Notes: SYNOPSIS. Endosymbiotic algae from Paramecium bursaria when added to the culture medium are ingested by Chlorella-bearing P. bursaria at a rate of 2,000 algae/organism/day. That the ingested algae are digested and assimilated by the ciliates is suggested by the more rapid growth of Paramecium when algae are added to the medium (G= 40 hr with algae compared to 190 hr without). The digestion by the ciliates of exogenous algae contrasts with the survival of these algae under normal growth conditions. It is suggested that the protection of the endogenous algae is related to their location in peripheral perialgal vacuoles.

Notes: SYNOPSIS. Toxoplasma ranae sp. n. is described from the brain of a leopard frog, Rana pipiens, probably from Mexico. Its pseudocysts were 72(55-106) × 48(29-70) μm in fixed sections. They contained an average of ∼ 4,000 slightly curved elongate zoites measuring 4–5 × 0.5 μm, with a central, spherical, vesicular nucleus.

Notes: Book reviewed in this article:Pennycuick, C. J. 1974. Handy Matrices of Unit Conversion Factors for Biology and Mechanics.

Notes: SYNOPSIS. Egestion of carmine particle-containing food vacuoles from the cytoproct of Tetrahymena pyriformis has been analyzed by high-speed cinemicrography. The vacuole may enter into position in the cytoproct ∼ 7 sec before ejection, and forms a distinct bulge beyond the outline of the cell surface for over 2 sec prior to ejection. The ejection process itself requires 20–80 msec.

Notes: SYNOPSIS. Blood films were examined from 1477 birds of Taiwan (193 species, 49 families). Haemoproteus Kruse was by far the commonest parasite, with Leucocytozoon Danilewski a not very close second. It is probable that some of the Haemoproteus infections represented new species, and 1 occurring in the Bamboo Partridge (Bambusicola thoracica sonorivox Gould) seemed characteristic enough to justify recognition as such; the name Haemoproteus bambusicolae sp. n. is proposed for this organism. Malaria was found in 77 birds, the greatest number of infections occurring in the Bamboo Partridge. Most of them were caused by Plasmodium juxtanucleare Versiani & Gomes, a pathogen of chickens, but a number were due to an undetermined species of Plasmodium. The Bamboo Partridge may be a reservoir host of the former. A few other identified species (P. rouxi Sergent & Sergent, P. hexamerium Huff, P. tenue Laveran & Mesnil) were seen, as well as some unidentified ones. Plasmodium tenue was seen in Garrulax canorus taewanus Swinhoe, a babbler: until now it was known only from the Pekin Robin (Leiothrix luteus Scopoli), also a babbler, in which we have found it extremely common. Sixty-four microfilarial infections were identified; they were especially frequent in the Button Quail (Turnix suscitator rostrata Swinhoe).

Notes: SYNOPSIS. Short pulse-labeling of log phase Crithidia fasciculata cells with [3H]thymidine allowed the autoradiographic visualization of 2 sites of replication of kinetoplast DNA situated at the periphery of the networks and separated by 180°. Longer pulse-labeling led to the previously reported total peripheral labeling pattern. Pulse-labeled networks possess an intermediate density in ethidium bromide-CsCl equilibrium gradients between the densities characteristic of closed networks and open or linear DNA. Removal of ethidium bromide by several methods and treatment of intermediate band networks with RNase and pronase had no effect on the equilibrium rebanding pattern. Closed minicircles of Leishmania tarentolae are not labeled by a short pulse of intact cells with [3H]thymidine. A chase of ∼ 3–4 hr is required for the appearance of radioactivity in closed minicircles, a time delay which implies the existence of intermediate events between replication and eventual covalent closure of the minicircles.

Notes: SYNOPSIS. DNA synthesis during growth and differentiation in Naegleria gruberi strain NEG populations has been studied. Autoradiography of cells labeled with [3H]thymidine revealed that grains are concentrated over the nuclei in logarithmically growing populations of cells, whereas in differentiating cells, grains are scattered over the cytoplasm; i.e. no significant nuclear labeling is detectable. It was established by MAK chromatographic analysis that [3H]thymidine is incorporated into double-stranded DNA in Naegleria and that the actual amount of incorporation in the logarithmically growing populations of cells is 20 times greater than that in differentiating cells. These results suggest that nuclear DNA synthesis is reduced markedly soon after the initiation of differentiation, while cytoplasmic DNA synthesis continues. It was established from cell cycle analysis that the approximate intervals of G1, S, G2, and M phases were 180, 183, 90, and 28 min, respectively. Hence, the reduction in the nuclear DNA synthesis in differentiating cells is not due to the inhibition of initiation of DNA replication, but rather to the termination of the DNA replicating process. Thus DNA synthesis is curtailed in the presence of RNA and protein synthesis which are required for differentiation.

Notes: SYNOPSIS. The activity and sedimentation of acid phosphatase (APase), acid deoxyribonuclease (DNase), and acid ribonuclease (RNase) were investigated throughout growth and encystment in Acanthamoeba castellanii. The activities/mg protein of all 3 hydrolases are high in young cultures and decrease to constant levels in postlog cells. The RNase activity/ ameba decreases 50% during growth, whereas the activity/cell of both APase and DNase remains constant. The percent sedimentation at 20,000 g of all 3 enzymes gradually increases from about 40% in midlog to a plateau of 80% in postlog cells. During encystment, the sedimentation behavior of RNase differs from that of APase and DNase. Encystment is characterized by a differential decrease in the activity/cell of the 3 hydrolases, with RNase decreasing most rapidly and APase least rapidly. APase is unique in that a transient increase of its specific activity is noted during encystment, even though its activity/cell is decreasing.

Notes: SYNOPSIS. In cultures of Platymonas subcordiformis Hazen, grown in appropriate light-dark cycles, as many as 75% of the cells adhered to the surface of the glass culture vessel toward the end of the light period of each day. Cell division occurred primarily while the cells were attached. Subsequently, motile daughter cells were released into the growth medium by the rupture of the mother cell theca. The settling behavior appears to be an integral part of the life cycle being synchronized to the same extent as cell division.

Notes: SYNOPSIS. The coccidian parasite Eimeria gadi was found in the haddock, Melanogrammus aeglefinus, taken from the Nova Scotian fishing banks. The haddock infection rates ranged from a high of 58% on Emerald Bank to a low of 4% on Georges Bank, the average being 32%. There was no relationship between sex and degree or prevalence of infection. Although the probability of an occurrence of infection increased with size, small fish with heavy infections were observed. The degree of infection had no apparent effect on the condition factor (length/weight) of the fish. The infection rate reached a maximum in the fall of the year while the heaviest infections were observed in the spring. It is evident from the data that the infection is fatal.The parasite mass, appearing as a creamy viscous to a yellow semisolid material in the swimbladder, consisted of various parasite stages, fibrous and cellular debris, and lipid material. Some aspects of the sporocyst stage are described.No other gadoids from the Nova Scotian banks were found to be infected; however, a single specimen of the fourbeard rockling, Enchelyopus cimbrius, from St. John's, Newfoundland, was found to be heavily infected with E. gadi.

Notes: SYNOPSIS. Synthesis of RNA in the macronucleus and appearance of RNA in the cytoplasm were studied in heat synchronized Tetrahymena pyriformis GL and compared to those found under conditions of logarithmic growth (28 C) and during heat shocks (34 C).In macronuclei of logarithmically growing cells precursors were processed to 2 rRNA species (25S and 17S). In addition, another RNA (15S), more homogeneous than the RNA (8-15S) in the cytoplasm, was observed in the macronucleus. Both 17S and 25S rRNA species were found in the cytoplasm, 17S rRNA appearing more rapidly than 25S rRNA. Synthesis of rRNA was suppressed at 34 C in cells subjected to heat synchronization; 8-15S RNA synthesis appeared to be inhibited to a lesser extent.During the time preceding the first synchronized division, the synthesis of rRNAs in the macronucleus slowly recovered. Early in the cycle, almost no newly synthesized rRNAs were extracted. By 30 min after the last heat shock (EH), most of the RNA synthesized was not identified as rRNA. By 60 min after EH, the pattern of RNA synthesis had not returned to that observed in logarithmically growing cells.

Notes: SYNOPSIS. Cell-free preparations of Acanthamoeba castellanii trophozoites transfer glucose from UDP-[U-14C]glucose to a chloroform-soluble form. This radioactive material has been isolated by thin-layer chromatography; it contains an alkali-labile and an alkali-stable (unsaponifiable) component. Treatment of the enzymic product with 0.1 N KOH for 15 min at 0 C or 20 C releases radioactivity into the aqueous phase as glucose. During this treatment, 30–60% of the original glycolipid remains chloroform-soluble. It is considered to be an alkali-stable glycolipid because no further loss of radioactivity occurs during an additional 45-min of treatment with 0.1 N KOH. During incubation with 0.1 N HCI at 100 C glucose is released quantitatively from both the untreated glycolipid and the alkali-stable glycolipid with a half-time of 6 min. Glycolipid formation is inhibited by UDP and is reversible; extracts catalyze the formation of UDP-glucose from the alkali-stable glucolipid and UDP.The chemical and physical properties of the alkali-stable glycolipid are consistent with a glucosyl phosphoryl polyprenol structure. Extracts prepared from cysts catalyze the formation of glycolipids aiso, but the glucosyltransferase activity/cell decreases during the course of encystment. Radioactivity is incorporated into the fraction insoluble in chloroform-methanol-water (1:1:1:) during these incubations when UDP-[U-14C]glucose or [14C]glycolipid is the substrate.

Notes: SYNOPSIS. In populations of Euglena gracilis strain Z synchronized by cultivation on a repetitive light-dark cycle, chloroplasts undergo cyclic changes in structure. During most of the light period chloroplasts are relatively compact with closely appressed lamellae; during the dark (division) period the chloroplasts become quite distended. This change persists for at least one cycle even when the cells are left in continuous light, suggesting that the periodicity may be related more to the age of the cell than to a direct effect of light. In addition, the pyrenoid in synchronized cells has a transient existence, being present only in the first half of the light period.

Notes: SYNOPSIS. Although large hemoglobin inclusions are observed in intraerythrocytic Babesia microti parasites, they are absent from parasites freed of hamster red cells by immune lysis with antihamster erythsocyte serum. Babesia microti has no cytostome. This parasite, therefore, does not appear to feed by phagocytosis of large boluses of hemoglobin, as does Plasmodium. To determine whether Babesia can pinocytose protein, free parasites were fed ferritin in an in vitro system. Ferritin was taken up from the entire cell surface into narrow channels within 15 min at 37 C. Only merozoites, with their pellicular complex, failed to take up the protein. By 60 min, the ferritin was highly concentrated in many channels and vesicles, which formed interconnecting stacks. The ferritin-containing channels became associated with membrane whorls of the multimembranous structure. Membrane whorls were also observed in the process of extrusion in samples incubated for longer times. These events may represent steps in the digestion and excretion of the pinocytosed protein. Empty channels formed when Babesia was fed albumin. The diaminobenzidine reaction for hemoprotein was positive for the channels in both free and intraerythrocytic babesias. The staining reaction was completely inhibited by cyanide, but not at all by aminotriazole. These results further suggest that Babesia pinocytoses hemoglobin in vivo. Plasmodium lophurae parasites freed of red cells by immune lysis are surrounded by 2 membranes and apparently can ingest ferritin only through the cytostome. Extracellular cytostomal feeding involves both membranes, as it does in vivo. Ferritin was found in food vacuoles, some of which contained hemoglobin ingested before parasite isolation, connected to or near the cytostome. In both Plasmodium and Babesia low temperature inhibited ferritin uptake.

Notes: SYNOPSIS. During the course of infection in the rat, Trypanosoma lewisi produces 2 antigenic variants: the 1st represents the initial, reproducing population of cells; and the 2nd the nonreproducing, ablastin-inhibited adult population. The specificities of the agglutinins elicited by the variants were studied by adsorption and agglutination methods and the newer immunoelectroadsorption technic. It was found that the reproducing variant has a surface antigen that reacts with the agglutinin specific for the adult variant, but this antigen does not become immunogenic until transformation to the adult variant occurs. It was also found, with fractions of immune sera obtained by gel filtration, that the agglutinin specific for the reproducing variant is IgG and that specific for the adult variant, IgM. The antigenic variants of pathogenic and nonpathogenic trypanosomes are compared, and the roles of trypanocidal and ablastic antibodies in the induction of antigenic variation are discussed.

Notes: SYNOPSIS. Living Trypanosoma musculi bloodstream trypomastigotes were agglutinated specifically with concanavalin A (ConA), wheat germ agglutinin (WGA), soybean agglutinin (SBA), and fucose-binding protein (FBP). The agglutination with these lectins of living cells from which the coat was removed by trypsinization was the same as with intact trypanosomes. Glutaraldehyde or formalin fixation did not affect the results with regard to agglutination with WGA, SBA, and FBP, but lower agglutination with ConA was observed upon fixation. By using a dense iron-dextran marker many fewer ConA marker particles were localized at the fine structural level in the intact than in trypsin-treated trypanosomes. On the basis of the results obtained by agglutination and electron microscopy, it is likely that fixation cross-links intact surface-coat components associated with the ConA binding sites. It is evident from the studies in which lectins were employed that ligands containing α-D-mannose, N-acetylglucosamine, N-acetylgalactosamine, and α-L-fucose are randomly distributed in the outer surface of the pellicular and flagellar membranes of T. musculi trypomastigotes. Results obtained with α-amylase- and dextranase-treated trypanosomes suggested that lectin-binding sugar ligands in the cell surface were not directly associated with α-1,4 or repetitive α-1,6 glucan-bonded polysaccharide moieties. Similar conclusions can be drawn on the basis of neuraminidase treatment with regard to N-acetylated neuraminic acids.After thorough washing, intact, but not trypsin-treated trypomastigotes were agglutinated specifically with antisera against whole mouse serum and against mouse IgG. Evidently, adsorbed constituents of mouse serum are regular components of the T. musculi surface coat. After incubation in dilute whole mouse serum or in mouse IgG solutions, also the trypsinized cells were agglutinated by the 2 antisera. No such results were obtained with trypsinized cells incubated in serum-free buffers. It was concluded that mouse serum proteins were readily readsorbed on, and firmly bound to the trypsinized cells' surfaces. Specific agglutinations were obtained with trypsinized cells after incubation in dilute rat, rabbit, bovine, and human sera and in solutions of rat and rabbit IgG in reactions with the corresponding antisera. It seems, therefore, that the host serum proteins are adsorbed nonspecifically to the cell surface of trypsinized T. musculi bloodstream forms.When examined by electron microscopy, the intact trypomastigotes were covered by an ununiform, slightly granular, fibrillar extracellular coat, applied to the entire outer lamina of the pellicular and flagellar membranes. No indication of such a coat was noted in the trypsinized organisms. Flocculent surface coat-like matrix could, however, be discerned in cells which, after trypsinization, were incubated in various sera.

Notes: SYNOPSIS. Leptomonas pessoai from the reduviid hemipteron Zelus leucogrammus, was cloned. The original strain (ATCC 30252) and clones can differentiate from promastigote to opisthomastigote. Differentiation is faster at high temperature (37 C) and in a defined medium as compared with a complex medium. It is suggested that Leptomonas pessoai be designated Herpetomonas samuelpessoai.

Notes: Book reviewed in this article: Journal of Toxicology and Environmental Health. Vol. 1, no. 1, Sept. 1975. Hemisphere Publishing Corp.Maloine, S. A., ed. 1974. Diagnostique Immunologique des Parasitoses a Protozoaires et Helminthes.

Notes: SYNOPSIS. Haemogregarina bigemina was found in all Blennius pholis which exceeded 5.0 cm in length, but in none measuring less than 3.5 cm. No exoerythrocytic development was recorded. The first B. pholis eggs hatched in May while the first patent infections of H. bigemina occurred from September onward in metamorphosed fish. Consequently, if the life cycle of H. bigemina includes a vector, that organism is active between May and September at least. Circumstantial evidence indicates that the hematophagous isopod, Gnathia maxillaris and not leeches, could be a vector of H. bigemina. Developmental stages of sporozoa were found in a small number of the isopods which had fed on infected B. pholis but the parasites could not be identified as H. bigemina with certainty. Subcellular organization, typical of sporozoa, was recorded by electron microscopy of H. bigemina.

Notes: SYNOPSIS. Leptomonas pessoai promastigotes cultivated in a synthetic medium were agglutinated with concanavalin A (Con A). Agglutination was predominantly of the flagellar-flagellar type, and was inhibited with sucrose or α-methyl-D-mannoside.Cell surface polysaccharides and/or glycoproteins were demonstrated by several cytochemical methods at the fine-structural level. A Con A-horseradish peroxidase-diaminobenzidine (DAB) technic was used to detect Con A receptors in the pellicular membrane of the flagellar pocket region and in the flagellar membrane proper. Somewhat less of the Con A-DAB reaction product was observed in the pellicular membrane enclosing the rest of the cell.

Notes: SYNOPSIS. Phylogenetic relations are ultimately determined by homologous relationships, including both structural and functional data. Following the establishment of those relationships, the direction of evolutionary change must be determined using paleontologic, developmental, and especially morphocline, data. From that perspective the direction of subsequent development becomes clearer and the problems of origins become more explicit.Using the foregoing methodology it has been possible to identify plausibly monophyletic groups of animal protists or protozoa. Allowing for attendant difficulties, there nevertheless emerges certain fairly convincing generalities: (a) the predominantly pseudopodial forms, with a few minor exceptions, have direct origins from apochlorotic algae; (b) the predominantly kinetidal forms (zooflagellates and ciliates), though also derived originally from apochlorotic algae, give evidence of extended evolutionary development with the especially noteworthy emergence of a permanent ingestatory structure; (c) both groups have increased size, a tendency towards multinuclearity and polyploidy, cytoplasmic differentiations of various sorts, and complex life cycles.In terms of further evolution, namely the emergence of multicellular animals, the pseudopodial forms are almost certainly a dead end while the kinetidal forms are arguably the ancestors of at least 2 metazoan phyla.

Notes: SYNOPSIS. A clone of Cyclidium citrullus, adapted to growth at 18, 27, 37, 43, and 46 C had an optimum at 43 C, with 6.5 divisions/day. Transfer of cells previously grown at 43 or 46 C to 18 C resulted in death of most of the cells, transfer to 27 C increased the lag period, and transfer from 18 C to 37 or 46 C was followed faster division. All cells died at 48 C; some divided before death. At the temperatures employed maximum cell sizes (length and width) were achieved in the early log phase. At 43 C, however, the early log phase cells were smaller. Quantitative and qualitative differences in the free amino acids in the cells were found in ciliates grown at 18, 43, and 46 C; the highest amount/cell was found at 18 C, and the lowest at 43 C. High concentration of proline was noted only at 18 C.

Notes: SYNOPSIS. Additional information on host interactions with trypanosomatid membranes was obtained from studies of a monomorphic strain of Trypanosoma brucei harvested at peak parasitemia from intact and lethally irradiated rats. Pellets of trypanosomes were fixed briefly in glutaraldehyde and processed for thin section electron microscopy or freeze-cleave replicas. Observations of sectioned material facilitated orientation and comparison of details seen in replicas. Fracture faces of cell body and flagellar membranes as well as 3-dimensional views of the nuclear membrane were studied. Cell body membranes of 80% of the organisms from intact rats contained random arrays of intramembranous particles (IMP). Aggregated clusters of particles appeared on the fracture faces of 20% of the trypanosomes. Some of these membranes had nonrandomly distributed particles aligned in distinct rows on the outer fracture face of both cell body and flagellum. Many inner face fractures of the cell body membranes had a particle arrangement similar to the longitudinal alignment of cytoskeletal microtubules. No aggregated particle distribution was seen in membranes of trypanosomes harvested from lethally irradiated rats. Replicas of trypanosome pellets also had plasmanemes as a series of attached, empty, coated membrane vesicles. These structures were found in close association with, as well as widely separated from the parasites. The shedding of these vesicles and the variation of particles in cell body membranes are discussed in light of antibody-induced architectural and antigenic changes in surface properties of trypanosomatids.The convex face of the inner membrane of the nucleus also is covered with randomly arrayed particles. More IMP were observed on the inner than on the outer nuclear membranes. Images of nuclear pores were also seen. The importance of these structures in drug and developmental studies of trypanosomes is discussed.On fracture faces of the flagellar membrane there were miniature maculae adherentes, unique to the inner fracture face and occurring only at regions of membrane apposition between cell body and flagellum. Each cluster of particles exposed by the freeze-cleave method corresponds to an electron-dense plaque seen in thin section images. However, because of a unique fracture pattern, these plaques were not revealed on the apposing body membranes, as illustrated in thin sectioned organisms.

Notes: SYNOPSIS. Phytomonas davidi (Trypanosomatidae) originally discovered by Lafont in 1909 on the island of Mauritius was rediscovered in Euphorbia cyathophora in Florida. Successful cultures were established in diphasic medium consisting of duck blood agar and modified Phillips’medium as overlay. Optimal growth was obtained when Mansour's medium was used as overlay and poorest growth when Cowperthwaite's medium buffered at pH 5.0 was utilized for this purpose. Marked changes tending toward choanomastigotes rather than the elongate twisted promastigotes were observed in cultures.

Notes: SYNOPSIS. Past reports of Synophrya, the only apostome ciliate known to harm its host, indicated that it was restricted in its distribution and in the hosts it can infect. In recent collections of decapods from the off-shore waters of North Carolina and Georgia, 30% of all specimens were infected with Synophrya. Forty-four percent of all the species collected had individuals infected with Synophrya, and 63% of all the families collected contained species that had infected individuals. There is no obvious structural or phylogenetic relationship between these families that explain why they are infected. The presence of Synophrya may be related to salinity since decapods captured in estuaries were never infected and decapods captured close to shore were only rarely infected. The salinities of these waters range from 15–35%, but the salinity of the off-shore waters where the great majority of infected specimens was found ranges only from 35–36%.

Notes: Book reviewed in this article:Pirt, S. J. 1975. Principles of Microbe and Cell Cultivation.

Notes: SYNOPSIS. Plasmodium lophurae serine hydroxymethyltransferase (EC 2.1.2.1) was partially purified and characterized by (NH4)2SO4 fractionation and chromatography on Sephadex G-100. The enzyme, precipitated by 3.0–3.3 m (NH4)2SO4, had a molecular weight of 68,300 as estimated by exclusion chromatography on G-100. The pH optimum of the enzyme was 6.8–7.6 in sodium phosphate-citrate buffer. Citrate stabilized the enzyme during storage in phosphate buffer at 4 C. The Km was 4.3 × 10−3m for l-serine and 2.5 × 10−4m for tetrahydrofolate.

Notes: Book reviewed in this article:Cordero del Campillo, M. et al. 1975. Indice-Catalogo de Zooparasitos Ibéricos. I. Protozoos. II. Trematodos.

Notes: SYNOPSIS. Haemogregarina balli sp. n. is described from the blood and organs of the common snapping turtle Chelydra serpentina serpentina and from the gastric and intestinal ceca of the presumed invertebrate hosts, the leeches Placobdella parasitica and Placobdella ornata. In the peripheral blood of the turtle, male and female gametocytes and immature erythrocytic schizonts are found within erythrocytes. The maturation of erythrocytic schizonts containing 6–8 merozoites is recorded from liver imprints. Schizonts with 13–25 merozoites are found in various cells of the liver, lung and spleen. In the gastric ceca of the leeches the host erythrocytes are digested, releasing the gametocytes and immature erythrocytic schizonts. Immature erythrocytic schizonts degenerate. Association of the gametocytes occurs in the intestinal ceca. The microgametocyte apparently gives rise to 4 nonmotile microgametes, one of which fertilizes the macrogamete while the other remain as condensed, residual nuclei on the periphery of the developing oocyst. The oocyst increases in size with maturity. A mature oocyst produces 8 sporozoites from a single germinal center. Sporozoites liberated from the oocyst are found in the tissues of the leech. Transovarial transmission of the parasite does not occur in the turtle. Attempts at experimental transmission failed. Previously unfed (control) leeches were negative for the parasite. Haemogregarina balli is compared with other haemogregarines described from C. serpentina. Features of species of Haemogregarina and Hepatozoon as well as the taxonomy of these genera are discussed.

Notes: SYNOPSIS. In low viscosity media, Euglena gracilis strain Z responds to a sudden change in light intensity by a cessation of forward movement, followed by a reorientation of the locomotor flagellum which results in turning of the cell around the lateral axis (photophobic response). At a viscosity interface between low [∼ 1 cP (centipoise)] and high (4000 cP) media, the cells exhibit avoidance responses or become immobilized in the higher viscosity medium. Upon changing the light intensity, free swimming cells have photophobic responses, while immobilized ones undergo body contractions. For cells immersed in media of varying viscosity, the delay between light stimulation and body contraction (transduction time) is shortest at high viscosities. From 500 to 2000 cP, where the cells are capable of both movement and light-induced body contractions, there is a logarithmic dependence of the transduction time on the viscosity. The transduction time does not vary appreciably with the intensity of the primary light stimulus within a range of 0.14-1.13 kW/m2.

Notes: SYNOPSIS. Eight species representing 8 genera of gallinaceous birds were used: Alectoris graeca; Colinus virginianus; Coturnix coturnix; Gallus gallus; Meleagris gallopavo; Numidia meleagris; Pavo cristatus; Phasianus colchicus. Three-week-old birds were dosed with sporulated oocysts of Eimeria tenella Beltsville strain. At 4, 24, 48, 72, 96, 120, 144, and 168 hr after inoculation, 1-3 infected birds and uninoculated controls of each species were killed by cardiac exsanguination. Pieces of intestines were fixed and examined for stages of E. tenella as stained paraffin sections or indirect fluorescent antibody preparations. Oocyst counts were made in droppings collected for the first 6 days of the patent period. Sporozoites were found in the lamina propria of some birds of 5 species at 4 hr postinoculation, but no stages were found thereafter except in the breeds of G. gallus and A. graeca. At 144 and 168 hr postinoculation, a few macrogametes were found in the ceca of 2 A. graeca, but no oocysts were found in the feces. No statistical difference was found between the number of oocysts produced/bird in the breeds of G. gallus examined. It is evident from these observations that E. tenella did not complete its life cycle in several close phylogenetic relatives of G. gallus, even though in other studies this parasite was found to complete its life cycle in cell cultures derived from the same birds.

Notes: Book reviewed in this article:Faust, E. C., Beaver, P. C. & Jung, R. C. 1975. Animal Agents and Vectors of Human Disease.

Notes: SYNOPSIS. A video technic is described that permits a quantification of the degree of attraction of Trypanosoma cruzi trypomastigotes to vertebrate cells in vitro. Bovine embryo skeletal muscle cells (BESM), HeLa cells and Vero cells all attract a myotropic strain of T. cruzi trypomastigotes. BESM cells, however, are 2-fold more attractive to trypomastigotes than HeLa cells and 10-fold more attractive than Vero cells. Heat-inactivation of BESM cells abolishes their ability to respire and also to attract T. cruzi trypomastigotes. As there is no difference in the endogenous oxygen consumption between BESM, HeLa, and Vero cells, it is unlikely that differences in the attraction of trypomastigotes to the 3 cell types are due to variations in the magnitude of pO2 or pCO2 gradients in the milieu around the cells.

Notes: SYNOPSIS. Euglena gracilis strain Z has a motor response which results in orientation with respect to the polarization of a light stimulus. Cells swim preferentially in a direction perpendicular to the plane of polarization of the stimulus. If 2 polarized stimuli are given from opposite directions, the preferred direction is, under certain circumstances, at right angles to the directions of both stimuli. Euglena also preferentially assumes an orientation that is at right angles to the force of gravity. The relationships between these responses and phototactic movements oriented with respect to the direction of the stimulus are discussed.

Notes: SYNOPSIS. The behavior of Paramecium caudatum in small capillary glass tubes was investigated under various ionic conditions and at the various tube diameters. Along the inner walls of the tubes ciliates undergo regular spiral motion, which is completely different from natural spirallings or random walk-like movements observed usually in large vessels. The curvature calculated from the tracks of spiral motions was independent of the inner diameters of capillary tubes, but depend specifically on ionic conditions.A plausible law governing such regular spiral motions of Paramecium caudatum is proposed. A definite part of the anterior end of a ciliate seems to contact the curved surface of the inner wall of a capillary tube during the motion so that the organism receives a constant tactile stimulus, and the direction of motive force keeps a certain angle against the surface.

Notes: SYNOPSIS. Observations of the ultrastructure of marine scuticociliatids, tentatively assigned to the genus Uronema, were made by light, transmission electron, and scanning electron microscopy. Giant, cortically oriented mitochondria filled the subpellicular, intermeridional areas, and were in close association with the epiplasm immediately under the inner alveolar sac membranes. Reconstructions of serial sections of the posterior poles of ciliates indicated that the intermeridional mitochondria could fuse at that point and the entire chondriome might at times be a single organelle. A system of tubules was observed to be intimately associated with the mitochondria in the posterior region. The tubules anastomosed and were directed posteriorly into the region of the nephridial-contractile vacuole system. The outer surfaces were coated with projections arranged in helical patterns. The system may be regarded as a fluid segregation organelle. The tripartite nature of the polar basal body complex observed by silver impregnation was confirmed by transmission electron microscopy. The 3 structures were the basal body of the caudal cilium and 2 parasomal sacs. A prominent ring around the caudal cilium was observed by scanning electron micrcscopy; it is probably responsible for the silver deposition surrounding the polar basal body complex that can be seen by light microscopy of silver-impregnated specimens. The ultrastructure of the nonmotile caudal cilium and its kinetosome was unremarkable, being like that of the motile, somatic cilia. The micronuclear and macronuclear outer membranes were continuous at several sites. Such interconnections explain the intimate physical relationship between the nuclei during interphase in many ciliates, and could be a structural basis for chemical communication between the 2 nuclear types. Within the cytoplasm surrounding the opening of the cytoproct, numerous clear vesicles were observed. Their position and appearance suggested that the cytoproct may be involved in the elimination of solutions as well as solids. Food vacuoles, cortical microtubules, lamellar vesicles, disc-shaped vesicles, mucocysts, and a contractile vacuole and its pore were also observed.

Notes: SYNOPSIS. The occurrence and levels of activity of various enzymes of carbohydrate catabolism in culture forms (promastigotes) of 4 human species of Leishmania (L. brasiliensis, L. donovani, L. mexicana, and L. tropica) were compared. These organisms possess enzymes of the Embden-Meyerhof pathway but lack lactate dehydrogenase. No evidence could be found for the production of lactic acid by growing cultures and lactic acid could not be detected either in cell-free preparations or after incubation of cell-free extracts with pyruvate and NADH under appropriate conditions. All 4 species possess α-glycerophosphate dehydrogenase and α-glycerophosphate phosphatase which together could regenerate NAD, thus compensating for the absence of lactate dehydrogenase. The oxidative and nonoxidative reactions of the hexose monophosphate pathway are present in all 4 species. Cell-free extracts have pyruvate dehydrogenase activity which allows the entry of pyruvate into and its subsequent oxidation through the tricarboxylic acid cycle. All enzymes of this cycle, including a thiamine pyrophosphate dependent α-ketoglutarate dehydrogenase are present. Both NAD and NADP-linked malate dehydrogenase activities are present. The isocitrate dehydrogenase is NADP specific. There is an active glutamate dehydrogenase which could compete with α-ketoglutarate dehydrogenase for the common substrate (α-ketoglutarate). Replenishment of C4 acids is accomplished by heterotrophic CO2 fixation catalyzed by pyruvate carboxylase. All 4 species have high levels of NADH oxidase activity. Several enzymes thus far not found in any species of Leishmania have been demonstrated. These are: phosphoglucose isomerase, triose phosphate isomerase, fructose-1, 6-diphosphatase, 3-phosphoglycerate kinase, enolase, α-glycerophosphate dehydrogenase, α-glycerophosphate phosphatase, pyruvate dehydrogenase complex, citrate synthase, aconitase, α-ketoglutarate dehydrogenase, glutamate dehydrogenase, and NADH oxidase.

Notes: SYNOPSIS. Oocysts of Isospora vulpina were found in silver foxes (Vulpes vulpes) on a fox farm in Wisconsin. They were 29.7 (25-38) × 24.3 (21-32) μm. The sporocysts were 17.7 (15–23) × 13 (11–16) μm. Five coccidia-free puppies were inoculated with 22,000–42,000 oocysts each of I. vulpina from the fox: a patent infection resulted after 6-7 days. The infection was then transferred from 1 of these dogs to another coccidia-free puppy. After a 7-day prepatent period the puppy passed oocysts for 7 days.

Notes: SYNOPSIS. In an electron microscopic study, counts of peripheral microtubules were made in spheromastigotes and trypomastigotes in tissue cultures of embryonic heart muscle cells. In interphase spheromastigotes there were, at the level of the nucleus, ∼ 114 microtubules; in dividing forms, there were ∼ 222. In trypomastigotes, the number of microtubules varied according to the level of the section—there were fewer than 40 tubules in the pointed ends of an organism, while in the central segment the number of these elements ranged from 60 to 115. The highest number of microtubules was found in the region containing the Golgi complex. The distance between the microtubules was constant, equalling 44 nm, even at the pointed ends of a trypanosome. This suggests that the microtubules course parallel to one another. Cross sections and randomly arranged, variable length, longitudinal sections of the tubules were noted around the kinetosomes in dividing organisms.

Notes: SYNOPSIS. An intracellular protozoon was discovered in the epithelium of young rainbow trout (Salmo gairdneri) exposed for as short a time as 1 hr to water known to contain infective stages of Myxosoma cerebralis. Light- and electron-microscopic examination of this tissue revealed what appeared to be a proliferative stage (presumptive schizont) of a sporozoon; other possible stages in the life cycle were also observed. The relationship of this unidentified protozoon to M. cerebralis remains unresolved.

Notes: SYNOPSIS. Coriphosphine staining of Stylonychia mytilus exconjugants at different times after separation reveals some details of the developing macronucleus. Green fluorescence is seen in both bands and heterochromatic blocks of the polytene chromosomes. No red fluorescence was observed along these chromosomes. Fragments of the old macronucleus and the pycnotic micronuclei have red or orange fluorescence. Red fluorescence is characteristic also of nucleoli in the new macronucleus.

Notes: SYNOPSIS. Trophozoites and other pre-spore stages of the myxosporidan Myxosoma cerebralis were taken from infected rainbow trout (Salmo gairdneri) and cultured in vitro. Cultures eventually yielded mature spores capable of discharging their polar capsules. This is the first report of culture of a myxosporidan.

Notes: SYNOPSIS. Conjugation in Paramecium tetraurelia can be induced within mating-reactive cultures of a single mating type by treating the cells with solutions of KC1 + acriflavine in culture medium low in Ca2+. Gene mutations with known physiologic effect were used as selective inhibitors of cell surface membrane function to see which functions are necessary for chemical induction of conjugation. The results strongly suggest that a transient increase in the internal concentration of calcium at the very beginning of chemical induction is a necessary but not sufficient step.

Notes: SYNOPSIS. In a method for isolating a relatively clean suspension of concentrated Plasmodium berghei ookinetes from infected midguts of Anopheles stephensi at appropriate times after the infective blood meal, the ookinetes are freed from the midguts by enzymatic digestion, and then concentrated by means of a BSA/renografin gradient. The mean number of ookinetes recovered/midgut was 152. More than 95% of the recovered ookinetes were viable by the criteria of motility, incorporation of adenosine and leucine, and appearance on light and electron microscopic examination. Trypan blue exclusion was not a valid criterion for viability. These ookinetes were not useful for in vitro studies of further development due to the presence of contaminating microorganisms. Our attempts to determine their potential for further development in vivo have similarly not been successful. Nevertheless, our ability to obtain large numbers of ookinetes at defined times during development now permits further studies on their structure, biochemistry, and physiology, as well as comparison with ookinetes formed in vitro.

Notes: SYNOPSIS. An extracellular surface coat was observed at the fine-structural level on the outer lamina of the pellicular and flagellar membranes of intact Trypanosoma musculi bloodstream forms. The surface coat had a mean width of 9.2 nm, and was composed of a somewhat electron dense, uneven, fibrillar-like matrix. Brief trypsin treatment of living blood forms completely removed the cell surface coat.Several cytochemical methods applicable to electron microscopy were used to detect the presence and distribution of carbohydrates in the trypanosome's surface coat and pellicular membrane. The polycationic dye compounds employed were: ruthenium red, ruthenium violet, Alcian blue chloride, and lanthanum nitrate. Electron-dense stain reaction products, indicative of polysaccharides, were evident in the surface coat of cells treated with these dyes, which also agglutinated both living and glutaraldehyde fixed cells. Like the surface coat, the pellicular membrane of trypsinized cells gave strong positive staining reactions with the several dyes, indicating the presence of membrane bounded carbohydrates, and living and glutaraldehyde-fixed trypsinized cells were agglutinated with the polycationic stains. Bloodstream forms were treated with the enzymes, α-amylase, dextranase, and neuraminidase. No obvious morphologic difference, however, was apparent between the surface coat of untreated cells and those subjected to treatment with any of the various glycoside hydrolase enzymes. Further, these enzymes had no apparent gross effect on the staining affinity of the surface coat for the several polycationic dyes. Cationized ferritin was used to visualize the negative cell surface charge of T. musculi bloodstream forms. Large quantities of cationized ferritin were bound in the surface coat matrix. Glycoside hydrolase enzyme treatments had no apparent effect on the amount of ferritin bound in the surface coat. Cationized ferritin was bound also to the outer lamina of the pellicular membrane in trypsinized cells, which had quantitatively less ferritin bound per surface unit area than bloodstream forms untreated by the enzyme. Living and glutaraldehyde-fixed cells were agglutinated with cationized ferritin. The results obtained in the various experiments indicated that polyanionic polysaccharides were constituent terminal ligands of the surface coat matrix and pellicular membrane in T. musculi bloodstream forms.

Notes: SYNOPSIS. The sporogonic stages of Leucocytozoon dubreuili in the midgut and salivary glands of the simuliid vectors was studied by electron microscopy. Young uninucleate oocysts have a pellicle that initially resembles that of the ookinetc. Numerous electron-dense bodies and microtubules in the peripheral cytoplasm may be involved in the formation of the cyst wall. The dense bodies appear to give rise to the amorphous material of the wall. The tubules which run circumferentially beneath the oocyst's boundary probably serve as a skeletal support for the cell surface during deposition of the wall material. A subcapsular “space” which provides area for expansion of the developing sporozoites is formed in early multinucleate oocysts. The subcapsular “space” appears to be formed through a condensation of the peripheral cytoplasm, resulting in an osmotic gradient across the oocyst's limiting membrane. Consequently water diffuses out, creating a fluid-filled space. Sporozoite formation begins with localized thickenings on the oocyst's limiting membrane. Subsequent extension of the thickened regions into the subcapsular “space” marks the onset of sporozoite budding. The process is highly synchronized, and culminates with the production of up to 150 sporozoites about the sporoblastoid body. The structure of sporozoites from mature oocysts and of the salivary glands of the vector is basically similar, although salivary gland sporozoites are more elongate and have numerous electron-dense micronemes. The paired rhoptries in the latter sporozoites are more elongate and uniformly electron-dense than in oocyst sporozoites.

Notes: SYNOPSIS. Temperature strongly influenced morphogenesis of intracellular trypomastigotes in cell culture infected with 2 different strains of T. cruzi. With the Gilmar strain the amastigote-to-trypomastigote differentiation readily occurred at 33 and 37 C, whereas with the CL strain differentiation took place at 33 C but was inhibited at 37 C. The possibility of this selective thermosensitivity resulting from mutational adaptation of the parasite is discussed.

Notes: La présence de diplocaryons à tous les stades de la sporulation d'Octosporea muscaedomesticae Flu, 1911 est mise en évidence ainsi qu'une membrane pansporoblastique autour des sporoblastes en développement et des spores. Le problème présenté par ces 2 faits est discuté. Une évolution étrange des ribosomes périnucléaires et démontrée. Une telle étude ultrastructurale est nécessaire et intéressante car O. muscaedomesticae est l'espèce-type du genre Octosporea.

Notes: SYNOPSIS. It is evident from studies of cellular recognition resulting in phagocytosis by Chaos carolinensis that cilia from certain protozoa serving as prey, e.g. Tetrahymena pyriformis, influence phagocytic action. Glutaraldehyde-fixed C. carolinensis to which cilia, isolated from Tetrahymena, are attached by the benzidine reaction, are engulfed by living Chaos but not digested. Fixed Chaos without attached cilia are not engulfed. Adding increased numbers of cilia from Tetrahymena progressively inhibits the rate at which Chaos phagocytizes Paramecium caudatum, suggesting blockage by the cilia of contact sites normally available to initiate phagocytosis of Paramecium.

Notes: SYNOPSIS. The microsporidan Glugea stephani is a common parasite of juvenile English sole (Parophrys vetulus) in Yaquina Bay, Oregon. Field observations indicated that fish became infected only in the upper estuary where summer temperatures were above 15 C and the incidence of infection reached 79.8% in the late fall.Laboratory infections developed and parasite growth occurred only at or above 15 C. The parasite was successfully transmitted to juvenile English sole by brine shrimp (Artemia salina) and amphipod (Corophium spinicorne) vectors as well as by direct ingestion of spores by the host. Infections that resulted from ingestion of spore-carrying vectors were much heavier than those resulting from the direct ingestion of spores. The speckled sanddab (Citharichthys stigmaeus), a nonpleuronectid flatfish, and chum salmon (Oncorhynchus keta) were refractory to G. stephani infection in the laboratory.Results of this study suggest that G. stephani is potentially lethal to young pleuronectid flatfishes when heavy infections involve the entire intestine and reduce the capacity to absorb nutrients. Under these circumstances, starvation is probably the direct or indirect cause of death. The restriction of infection to fish that reach the upper estuary very likely mitigates the impact of G. stephani caused mortality on the entire English sole population on the Yaquina Bay nursery ground.

Notes: SYNOPSIS. Optimal assay conditions are described for 8 hydrolases of Euglena gracilis var. bacillaris, SM-L1 (streptomycinbleached) strain, 7 of which have an acid pH-optimum. Acid phosphatase, β-galactosidase, β-glucosidase, β-fucosidase, cathepsin D, RNase, DNase, and an esterase are active in cell homogenates. Amylase has very low activity, and β-glucuronidase, arylsulfatase, β, N-acetyl-glucosaminidase, α-fucosidase, and α- and β-mannosidase are inactive.Hydrolase activity increases as a culture proceeds from the midexponential to the late stationary-phase of growth, being most pronounced in the case of β-glucosidase. In cultures deprived of a utilizable carbon source, the specific activities of the hydrolases (per mg total protein or dry weight) increase. When expressed on a per cell basis, however, the activities of DNase decrease while those of β-galactosidase, cathepsin D, and RNase increase. The hydrolases appear to be involved in the adaptation of Euglena to the metabolic demands imposed by different conditions of growth.

Notes: SYNOPSIS. Sensitivity to pentamidine of bloodstream forms and culture forms of Trypanosoma brucei brucei, strains of this subspecies, and strains of T. brucei rhodesiense characteristically differs in vitro. Analyses of transport parameters for pentamidine uptake in these organisms show differences that correspond with drug sensitivity. Long slender bloodstream forms of T. b. brucei have a high affinity for the drug and high rates of uptake as indicated by Km and Vmax values for [3H]pentamidine transport. Although pentamidine and stilbamidine resistance is associated with dyskinetoplasty. this condition does not itself confer resistance to pentamidine nor does it affect pentamidine transport. However, drug-resistant strains show lower rates for pentamidine transport as does T. b. rhodesiense, which is characteristically less sensitive to the drug. Of all the forms and strains studied, procyclic trypomastigotes were least sensitive to pentamidine and had a remarkable ability to exclude the drug.

Notes: SYNOPSIS. The 16S ribosomal RNA of the chloroplast of Euglena gracilis strain Z has been characterized in terms of its 2-dimensional electrophoretic “fingerprint” (T1 ribonuclease). Over 100 spots were resolved on the “fingerprint” and each spot was characterized as to which RNA oligonucleotide fragment(s) it contained. When compared to similar analyses of prokaryotic 16S rRNAs and eukaryotic cytoplasmic 18S rRNAs, the chloroplast 16S rRNA was a typically prokaryotic RNA, but bore little if any relationship to eukaryotic 18S rRNAs. Therefore, the cistrons for chloroplast 16S rRNA are related to the equivalent prokaryotic cistrons, but, apparently, are not related to the equivalent eukaryotic cistrons. Among the organisms available for comparison, the Euglena chloroplast 16S rRNA appears most closely related to the 16S rRNA of the eukaryote, Porphyridium cruentum (a red alga), and at least distantly related to the 16S rRNAs of the blue-green algae and perhaps also to the bacilli.

Notes: SYNOPSIS. A survey of 22 Western Painted Turtles (WPT), Chrysemys picta belli Gray; 2 Map Turtles (MT), Graptemys geographica Le Sueur; 8 False Map Turtles (FMT), Graptemys pseudogeographica Gray; 26 Illinois Mud Turtles (IMT), Kinosternon flavescens spooneri Smith; and 5 Spiny Softshell Turtles (SST), Trionyx spiniferus Le Sueur, revealed the presence of 10 species of coccidia. The species found, the shape and average length-width dimensions (in micrometers) of their oocysts, and the respective hosts from which they were isolated were as follows: Eimeria chrysemydis Deeds & Jahn, slightly pear-shaped (27.6 × 17.0), from 5 WPTs; Eimeria delagei marginata Deeds & Jahn, markedly pearshaped (22.1 × 17.6), from 2 WPTs, 1 MT, and 3 FMTs; Eimeria graptemydos sp. n., broadly ellipsoid to subspherical (12.6 × 11.4), from 10 WPTs, 2 MTs, and 5 FMTs; Eimeria lutotestudinis sp. n., broadly ellipsoid to subspherical (11.9 × 10.8), from 4 IMTs; Eimeria mascoutini sp. n., broadly ellipsoid to subspherical with outer surface of oocyst wall mammillated (14.0 × 11.9), from 2 SSTs; Eimeria mitraria (Laveran & Mesnil), asymmetrically ellipsoid, bearing 1 or 2 conical projections at the polar end and 2 or 3 at the antipolar end (10.0 × 7.6), from 7 WPTs, 1 MT, 3 FMTs, and 4 IMTs; Eimeria pseudogeographica sp. n., narrowly ellipsoid to slightly ovoid (19.5 × 13.5), from 5 WPTs and 3 FMTs; Eimeria tetradacrutata sp. n., spherical to subspherical with outer surface of oocyst wall mammillated (19.5 × 19.2), from 1 WPT; an Eimeria sp. narrowly ellipsoid, bearing 2 conical projections at the polar end and 2 at the antipolar end (23.8 × 13.2), from 1 MT; and Mantonella hammondi sp. n., conical to narrowly ellipsoid, bearing 1 conical projection at the polar end and 2 or 3 at the antipolar end (14.3 × 7.1), from 1 IMT. The overall infection rate for the 63 turtles examined was 54.0%.

Notes: SYNOPSIS. The schizont stage of 3 strains of the testate marine ameba, Trichosphaerium sp., was examined in the transmission electron microscope. The cytoplasm of this multinucleate organism contained the usual organelles; the test was covered by spicules. Pseudopodial types included broad ectoplasmic lobopods that assisted in locomotion, and thin dactylopods that probably had a sensory function. Nuclear division, observed in one of the strains, was characterized by an intact nuclear envelope (at least through anaphase), and the absence of centrioles. Nuclei in an ameba divided synchronously. An unusual intranuclear body of unknown function was found in another of the strains examined.

Notes: SYNOPSIS. The fine-structural aspects of development of microgamonts of Eimeria magna were studied in kidney cell cultures and in experimentally infected rabbits. Spheroidal masses of gamont-like cytoplasm containing ribosomes, polyribosomes, and amylopectin granules were found within the parasitophorous vacuole; these bodies were apparently pinched off the surface of the gamont. Nucleoli were present in the early stages of nuclear division but disappeared as development proceeded. Spindles were eccentric and the nuclear membrane always remained intact in dividing nuclei. Nuclei eventually became elongate in shape, compact, and electron dense at the end oriented toward the periphery and lucent centrally. Usually, only the dense portion was incorporated into the gamete as the gamete developed by protruding from the gamont surface. Fullyformed microgametes were biflagellate and contained a nucleus, a mitochondrion, and 8-10 microtubules. Multiple-membrane complexes, which apparently originated from the nuclear envelope or endoplasmic reticulum, were found within the gamont residual body. Occasionally, 2 or 3 micro- and/or macrogamonts were seen within the same cell. In some cells one or 2 micro- or macrogamonts as well as several merozoites were present in the same parasitophorous vacuole.

Notes: SYNOPSIS. Oxytricha fallax and Stylonychia pustulata possess 6 rows of dorsal bristle units. Each dorsal bristle unit consists of a pair of kinetosomes; the anterior kinetosome has a cilium and the posterior kinetosome a ciliary stub. The kinetosome pair, located at the bottom of a cortical pit surrounding the cilium and ciliary stub, is surrounded by an asymmetrical fibrillar mass. Future rows 1-4 are formed from 2 sets of primordia originating within mature dorsal rows 1-3. Rows 5 and 6 originate from the anterior regions of both right marginal cirral primordia. Old dorsal bristle units utilized in formation of primordia are presumably maintained in the new rows of the proter and opisthe; those outside the primordia are resorbed. The morphogenetic pattern of the Oxytrichidae is similar to those of the Urostylidae and Holostichidae, but quite different from that of the Euplotidae.

Notes: SUMMARY. In water taken March 3, 1956, from a tributary of the Amazon River, near Leticia, Colombia, an abundant ciliate fauna included large numbers of a species of Euplotes. Cursory examination showed a pronounced left wing like that of E. novemcarinatus Wang. Careful study, however, revealed a distribution of peristomal membranelles and peristomal morphology more like that of E. euryostomus Wrzesniowski. The positions of ventral cirri resemble those of E. woodruffi Gaw. The two right caudal cirri are furcated, as are those of the first two above-mentioned species; but the five anal cirri are not. The C-shaped macronucleus, like that of E. aediculatus Pierson, has the upper left part of the “C” somewhat depressed. A large organism, it averages 155 μ long by 130 μ broad, length ranging from 87 μ to 203 μ, and width from 67 μ to 194 μ. It is presented as Euplotes leticiensis n. sp.

Notes: SUMMARY. Following a brief historical review and critique of the main theories of amoeboid movement, the recent work of Goldacre and Lorch, relating plasmagel contraction to the folding and unfolding of protein molecules, is discussed; and some new observations are presented concerning the behavior of the plasmagel in amoebae vitally stained with neutral red. Similarities between contraction of vertebrate muscle and amoeba plasmagel are discussed, and a summary of recent work suggesting that adenosine triphosphate and actomyosin-like proteins may be involved in amoeboid movement is given. A re-examination of the meaning of the terms plasmagel and plasmasol indicates their relative nature denoting only comparative degrees of viscosity. Recent observations as to the nature of the plasmalemma are reviewed, and evidence is presented for the existence of an external slime layer in Amoeba proteus (not in all amoebae), which slides over the visible pellicle carrying adherent foreign particles forward from the precaudal region. The inadequacy of the contracting gel tube theory for explaining many types of protoplasmic streaming is pointed out.

Notes: SUMMARY. Tillina magna is a large holotrichous ciliate, of the family Colpodidae, which normally forms resting cysts. These cysts, when formed in their natural environment, withstand drying. Active animals have been excysted from dirt collected more than 10 years ago. However, until recently, laboratory work on these, as well as on most other ciliate cysts, has been done on wet cysts. A method is described for producing viable dry cysts under laboratory conditions. It consists essentially of inducing the tillinas to encyst on prepared sections of grass stems. In this way dry cysts have been formed which are viable up to 4 months. These cysts, when first formed, can be activated simply by the addition of water. Cysts which are no longer responsive to water alone may sometimes be induced to excyst by the addition of lettuce infusion. Cysts withstand extremes of temperature from -5°C. to 45°C. These facts have some bearing on the question of the factor or factors causing excystment.

Notes: SUMMARY. A study has been made of the number and morphology of the chromosomes of five species of malarial parasites as seen in living material with phase contrast microscopy. Plasmodium knowlesi, of monkeys, is essentially similar to other primate malarial parasites previously studied, having two chromosomes of unequal length. P. lophurae, from ducks, P. relictum from pigeons and sparrows, and P. floridense from a lizard all have two small chromosomes of equal size. These facts, with ether data, indicate that the genus may consist of two species complexes. P. berghei, studied in white mice and rats, has a karyotype similar to the avian and saurian malarial parasites. The suggestion is made that P. berghei, on a basis of chromosome pattern and other characteristics, is probably more closely related to the avian and saurian species of Plasmodium than to other mammalian species.

Notes: SUMMARY. The adaptation to fatty acids by Polytoma depends upon two mechanisms: 1. The induced synthesis of fatty acid oxidase which precedes growth. 2. A long-term physiological adaptation spanning several cell generations which results in an increase of the initial rate of growth.Analysis of the long-term adaptation shows that the adaptation does not result from the selection of fast-growing mutants. The generation time on butyrate of unadapted cells is initially ca. 24 hours and it is reduced to ca. 10 hours after the second subculture in butyrate medium. Adaptation to butyrate results in a simultaneous adaptation to caproate.