Internalization of macromolecules from the medium in Suctoria

Takophrya infusionum like all other Suctoria lacks an oral cavity. Its feeding apparatus consists of tentacles, long narrow tubes through which the contents of the living prey are ingested. For normal growth, reproduction, and longevity of clones, Tokophrya needs supplements deriving from the medium in addition to living prey. Since Tokophrya lacks a mouth, these supplements can reach the cytoplasm only through the complex structure of the cortex, which is composed of a three- membraned pellicle and a dense epiplasm. In addition, external to the cortex, an extraneous coat covers the whole organism. Only the outer pellicular plasma membrane is continuous; the other two and the epiplasm are interrupted by the outer plasma membrane which invaginates at intervals forming the so-called pits. The invaginated plasma membrane dips down into the cytoplasm where it extends to form a saccule. Experiments with cationized ferritin and Thorotrast provide evidence that internalization of these macromolecules takes place through the pits by pinocytosis. The membrane of the saccules of the pits forms invaginations which pinch off giving rise to small, flattened vesicles containing the tracers. The tracers were never found free in the cytoplasm but exclusively in the flat vesicles. These vesicles are thus the vehicles transporting macromolecules from the medium to the cytoplasm. The saccules of the pits are the natural loci of pinocytosis and together with the flattened vesicles perform an important function in Suctoria, supplying the organisms with macromolecules from the medium.     

Configurational changes in helical microtubule frameworks in feeding tentacles of the suctorian ciliateTokophyra

Microtubules at the tip of a resting (non-feeding) tentacle are arranged helically in two concentric tube-shaped arrays. The pitches of the helical paths followed by tubules in the two arrays differ. At the start of feeding these microtubules bend along their longitudinal axes and splay outwards and downwards away from the tentacle tip as it ‘everts’. Tubules in the two arrays slideacross each other as this occurs. Comparison of the fine structure of the tips of feeding and resting tentacles with a dynamic model of the microtubular framework indicates that movement of the tubules is not brought about by active sliding of the tubules against each other or by the action of contractile elements attached along the lengths of tubules. The tips of microtubules forming the inner tube may be pulled downwards by contractile elements in the tentacular pellicle; these tubules apparently push those in. the outer tube to their new positions. The pattern of configurational changes in a tentacle tip at the start of feeding appears to be largely defined by the elastic resistance of the microtubules to bending, and the ways in which tubules are packed and linked together and attached to the pellicle.     

The Mechanism of Food Intake in Tokophrya infusionum and Ultrastructural Changes in Food Vacuoles during Digestion*

SYNOPSIS Food intake in Tokophrya infusionum is preceded by penetration of the knob of the tentacle into the cytoplasm of the prey, Tetrahymena. Immediately thereafter, the membrane of the knob starts to invaginate into the lumen of the inner tube of the tentacle carrying with it the cytoplasm of the prey. At the proximal end of the tentacle, the invaginating membrane inflates, pinches off and forms a food vacuole. The mechanism is similar to that in amoebae during pinocytosis. The first few food vacuoles contain broken-up membranes, an indication that predigestion of prey cytoplasm takes place. This process is limited, however, to the part of cytoplasm around the knob since all food vacuoles formed later are composed of intact cytoplasmic organelles of Tetrahymena. Among them the most abundant and at the same time the most resistant to digestion are mitochondria and mucocysts. The ultrastructure of mitochondria is preserved very well during processing for electron microscopy and changes in their fine structure therefore serve conveniently as markers of the stage of digestion and of the age of food vacuoles. Digestion of mitochondria progresses over a period of several hours. They finally seem to degrade into glycogen-like particles. All components of the food vacuole reach this stage much earlier. Digestion proceeds further until the food vacuole is filled with a watery content of very low density. Digestion in such food vacuoles is completed. The complete digestion of the content of food vacuoles is of primary importance for Tokophrya, since this organism does not have a cytopyge thru which waste products could be eliminated.     

MICROTUBULE ARMS AND CYTOPLASMIC STREAMING AND MICROTUBULE BENDING AND STRETCHING OF INTERTUBULE LINKS IN THE FEEDING TENTACLE OF THE SUCTORIAN CILIATE TOKOPHRYA

Microtubules attached to the pellicle at the tips of tentacles pivot through about 140° on these attachments, splay apart, and bend along their longitudinal axes when feeding occurs. The tubules could be bending in response to pellicular contractions; active bending, sliding, or contraction of the tubules may not be involved. Intertubule links apparently prevent tubules from splaying apart at certain levels. These links are probably under tension during feeding. They stretch; they sometimes become half as thick and eight times as long as they are before feeding. Often, tubules joined together by these links also change in shape; they become slightly flattened and elliptical in cross section. Cytoplasm from the ciliate Tetrahymena is drawn down a feeding tentacle inside an invagination of the Tokophrya cell membrane from the tentacle tip. The positions of arm-bearing microtubules around such invaginations indicate that arms are involved in moving invaginations along. The edges of the perforated Tetrahymena cell membrane are "sealed" to the cell membrane of Tokophrya around each feeding tentacle tip.     

The actin microfilament network within elongating pollen tubes of the gymnospermPicea abies (Norway spruce)

Summary Actin microfilaments form a dense network within pollen tubes of the gymnosperm Norway spruce (Picea abies). Microfilaments emanate from within the pollen grain and form long, branching arrays passing through the aperture and down the length of the pollen tube to the tip. Pollen tubes are densely packed with large amyloplasts, which are surrounded by branching microfilament bundles. The vegetative nucleus is suspended within the elongating pollen tube within a complex array of microfilaments oriented both parallel to and perpendicular with the growing axis. Microfilament bundles branch out along the nuclear surface, and some filaments terminate on or emanate from the surface. Microfilaments in the pollen tube tip form a 6 m thick, dense, uniform layer beneath the plasma membrane. This layer ensheathes an actin depleted core which contains cytoplasm and organelles, including small amyloplasts, and extends back 36 m from the tip. Behind the core region, the distinct actin layer is absent as microfilaments are present throughout the pollen tube. Organelle zonation is not always maintained in these conifer pollen tubes. Large amyloplasts will fill the pollen tube up to the growing tip, while the distinct layer of microfilaments and cytoplasm beneath the plasma membrane is maintained. The distinctive microfilament arrangement in the pollen tube tips of this conifer is similar to that seen in tip growth in fungi, ferns and mosses, but has not been reported previously in seed plants.     

Microtubules and microfilaments are both responsible for pollen tube elongation in the coniferPicea abies (Norway spruce)

Summary InPicea abies (Norway spruce), microtubules and actin microfllaments both form a dense matrix throughout the tube mainly parallel to the direction of elongation. In these conifer pollen tubes the organization of this matrix is different from that in angiosperms. This study tests our hypothesis that differences in cytoskeletal organization are responsible for differences in tube growth and physiology. Pollen grains were germinated in media containing cytoskeletal disrupters and analyzed for germination, tube length, tube branching, and tip swelling. Disruption of microtubules significantly inhibits tube elongation and induces tube branching and tip swelling. Tip swelling is probably caused by disruption of the microtubules in the tip that are perpendicular to the direction of elongation. Confocal microscopy indicates that colchicine and propyzamide cause fragmentation of microtubules throughout the tube. Oryzalin and amiprophosmethyl cause a complete loss of microtubules from the tip back toward the tube midpoint but leave microtubules intact from the midpoint back to the grain. Disruption of microfilaments by cytochalasins B and D and inhibition of myosin by N-ethylmaleimide or 2,3-butanedione monoxime stops tube growth and inhibits germination. Microfilament disruption induces short branches in tubes, probably originating from defective microfilament organization behind the tip. In addition, confocal microscopy coupled with microinjection of fluorescein-labeled phalloidin into actively growing pollen tubes indicates that microfllament bundles extend into the plastid-free zone at the tip but are specifically excluded from the growing tip. We conclude that microtubules and microfilaments coordinate to drive tip extension in conifer pollen tubes in a model that differs from angiosperms.     

Fast pollen tube growth in Conospermum species

BACKGROUND AND AIMS: An unusual form of pollen tube growth was observed for several Conospermum species (family Proteaceae). The rate of pollen tube growth, the number of tubes to emerge and the ultrastructure of these tubes are given here. METHODS: Pollen was germinated in vitro in different sucrose concentrations and in the presence of calcium channel blockers, and tube emergence and growth were recorded on a VCR. Measurements were taken of the number of tubes to emerge and rate of tube emergence. Pollen behaviour in vivo was also observed. The ultrastructure of germinated and ungerminated pollen was observed using TEM. RESULTS: After 10 s to 3 min in germination medium, up to three pollen tubes emerged and grew at rates of up to 55 micro m s(-1); the rate then slowed to around 2 micro m s(-1), 30 s after the initial growth spurt. Tubes were observed to grow in pulses, and the pulsed growth continued in the presence of calcium channel blockers. Optimal sugar concentration for pollen germination was 300 g L(-1), in which up to 81 % of pollen grains showed fast germination. Germination and emergence of multiple tubes were observed in sucrose concentrations of 100-800 g L(-1). The vegetative and generative nuclei moved into one of the tubes. Multiple tubes from a single grain were observed on the stigma. Under light microscopy, the cytoplasm in the tube showed a clear region at the tip. The ultrastructure of C. amoenum pollen showed a bilayered exine, with the intine being very thick at the pores, and elsewhere having large intrusions into the plasma membrane. The cytoplasm was dense with vesicles packed with inner tube cell wall material. Golgi apparatus producing secretory vesicles, and mitochondria were found throughout the tube. The tube wall was bilayered; both layers being fibrous and loosely packed. CONCLUSIONS: It is proposed that, for Conospermum, initial pollen tube wall constituents are manufactured and stored prior to pollen germination, and that tube extension occurs as described in the literature for other species, but at an exceptionally fast rate.     

Ultrastructural and Other Observations Which Suggest Suctorian Affinities for the Taxonomically Enigmatic Ciliate Cyathodinium*

SYNOPSIS. Two species of the taxonomically enigmatic genus Cyathodinium, C. piriforme and C. cunhai, were studied in some detail at both light and electron microscopic levels. Data obtained strongly suggest suctorian affinities for the genus, since a number of structures or features are strikingly reminiscent of similar (if not homologous) structures recently discovered in ciliates belonging to the order Suctorida. Endosprits (suctorial tentacles?) of Cyathodinium show an arrangement of microtubules not unlike that known for several suctorians, especially Acineta and Tokophrya. Haptocysts or missile-like bodies, ca. 600 mμ long, have been observed within endosprits and free in the cytoplasm; again this is reminiscent of the complex organelles recently described from several suctorian groups. Mouthlessness, coupled with the presence of a ventral depression (functioning in gathering prey at distal ends of endosprits?) and the presence of food vacuoles in the cytoplasm, further support a suctorian mode of feeding. Finally, stages in the curious life cycle of Cyathodinium suggest neoteny and a basic similarity to endogenous budding processes in certain suctorians.     

Differentiation of the tegument and associated structures in Diphyllobothrium dendriticum Nitsch (1824) (Cestoda: Pseudophyllidea). An electron microscopical study

Grammeltvedt Anne-François 1973. Differentiation of the tegument and associated structures in Diphyllobothrium dendriticum Nitsch 1824 (Cestoda : Pseudophyllidea). An electron microscopical study. International Journal for Parasitology3: 321–327. The differentiation of the tegument and associated structures of the coracidium, procercoid, plerocercoid and adult is described. The embryophore is composed of four zones and is covered by a fibrous layer resembling a glycocalyx. The oncospheral plasma membrane is extensively folded. A typical cestode tegument, with a distal and perinuclear cytoplasm, is probably already existing in the coracidium. The formation of the microvilli starts after about three days in the copepod host. In young procercoids ribosomes and Golgi complexes were observed in the distal cytoplasm. These organelles disappear at later stages. The infective procercoid has a typical tegument. The microvilli are shaped like a thorn compressed from the sides. They have an electron dense tip and a less dense base in which microfilaments are seen. Bodies, called disc-shaped and lamellated bodies, are described. The microvilli of the plerocercoid are characterized by a great variation in shape. The villi are bounded by two unit membranes. The lamellated bodies are especially well developed. The adult microvilli are uniform in shape. The lamellated bodies are few in young adults and disappear in mature worms.     

Impact of ivermectin on the ultrastructure of the testis of <Emphasis Type="Italic">Argas (Persicargas) persicus</Emphasis> (Ixodoidea: Argasidae)

Mated male Argas persicus were dissected 1 and 2 weeks after feeding on untreated and ivermectin (IVM)-treated pigeons. One week after feeding, testes of untreated ticks were filled with rounded spermatids with subplasmalemmal vesicles and cytoplasmic organelles, but lacking in treated ticks. Two weeks after feeding, testes were crowded with elongated spermatozoa supported by double-walled cisternal tubes. The tubes consisted of two opposite walls, each with outer-fringed processes and inner elongated cisternae. Both were supported with electron dense striated plates in the middle of the spermatozoon. Internally, the cisternal tubes contained mitochondria and vacuoles. The nuclei were elongated dense masses between the tubes and the cell membranes. Subcutaneous inoculation of IVM at the dose 400 μg/kg pigeon resulted in extensive alterations in the testis of A. persicus. IVM prevented the development of new spermatids. There was a break down of cell membranes and cytoplasmic organelles of spermatozoa. Multivesicular bodies and numerous vacuoles were noticed in their cytoplasm. Double membranes of elongated cisternae and striation of electron dense plates became indistinct. IVM caused granulation and vacuolization of the nucleus as well as injury of mitochondrial cristae. The results suggest that IVM may bind to the neurotransmitter or the hormone involved in the process of sperm development or may be toxic to the germinal cells of A. persicus testis.     

Fine structure of germinatingPenicillium megasporum conidia

Summary Penicillium megasporum conidia have spore walls consisting of several layers. There is no visible change in the outer wall layers during spore germination, but the inner layers increases in thickness on only one side of the spore, resulting in a rupture of the outer wall layers and subsequently in germ tube formation. Invaginations in the plasma membrane disappear as the germ tube forms and emerges, and the nucleus migrates into the developing germ tube. Mitochondria gather at the base of the germ tube during its formation. During germination, the amount of lipid in the spore decreases and portions migrate into the germ tube. Membrane-bound, electron dense bodies are present in resting spores. These bodies decrease in size as germination proceeds, and the cytoplasm in the developing germ tube appears much more electron dense than the cytoplasm within the spore.     

Metamorphosis in Tokophrya infusionum; an Electron-Microscope Study

SYNOPSIS. In Tokophrya infusionum metamorphosis from a ciliated swimming embryo to a sessile organism with a stalk, disc, and tentacles lasts only 3 minutes. The remarkable speed of meta-morphosis was clarified by an electron-microscope study of embryos before and during metamorphosis. Ultrathin sections have revealed that the embryo has at the anterior end of the body a number of specialized structures, such as dense bodies containing the precursor material for the disc and stalk, and microtubules which align the dense bodies into rows leading to pit-kite invaginations of the pellicle at the tip of the anterior end. At meta-morphosis the embryo settles down on this end and the precursor material is released thru the pits to the outside. At the same time the body of the embryo invaginates at this end, forming a cavity which becomes deeper and narrower until it acquires the shape of a channel. The 1st drops released from the dense bodies spread out on the substrate, forming the disc. The rest of the material, secreted into the channel, solidifies there to form the stalk. It seems obvious that the channel serves as a mold for the stalk, since after completion of the stalk the channel disappears. The stalk is structureless with no limiting membrane; it is outside the boundaries of the cell. Both the stalk and disc are extra-cellular organelles.
Of the new organelles appearing at metamorphosis, only the stalk and disc are formed de novo. The electron-microscope study disclosed that the embryo has internal parts of tentacles composed of a tube formed of microtubules. At the distal end of the microtubules is a ring of dense material. During metamorphosis the microtubules, together with the dense ring, grow out of the body, and along with them the pellicle and plasma membrane to form the external part of the tentacle.     

Development and cellular organization ofPinus sylvesfris pollen tubes

The organization ofPinus sylvestris pollen tubes during growth was studied by video microscopy of living cells and by electron microscopy after freeze-fixation and freeze-substitution (FF-FS). Pollen germinated and the tubes grew slowly for a total period of about 7 days. Some of the grains formed two tubes, while 10–50% of the tubes ramified. These features are in accordance with development in vivo. The cytoplasmic hyaline cap at the tip disappeared during the 2nd or 3rd day of culture. Aggregates of starch grains progressively migrated from the grain into the tube and later into the branches. Vacuoles first appeared at day 2 and eventually filled large parts of the tube. The tube nucleus was located at variable distances from the tip. Some of the organelles showed linear movements in a mostly circulatory pattern, but the majority of the organelles showed brownian-like movements. Rhodamine-phalloidin-stained actin filaments had a gross axial orientation and were found throughout the tube including at the tip. The ultrastructure of pollen tubes was well preserved after FF-FS, but signs of shrinkage were visible. The secretory vesicles in growing tips were not organized in a vesicle cone, and coated pits had a low density with only local accumulations, which is in accordance with slow growth. The mitochondria contained small cristae and a darkly stained matrix and were located more towards the periphery of the tube, indicating low respiratory activity and low oxygen levels. The dictyosomes carried typical trans-Golgi networks, but some contained less than the normal number of cisternae. Other elements of the cytoplasm were irregularly spaced rough endoplasmic reticulum, many multivesicular bodies, lipid droplets and two types of vacuoles. The typical organization associated with tip growth in angiosperm pollen tubes, e.g.Nicotiana tabacum, was not present inP. sylvestris pollen tubes. The different morphology may relate to the growth rate and not to the type of growth.     

Ultrastructural studies of the commensal suctorian,Choanophyra infundibulifera hartog

Summary Tentacle structure, movement and feeding of the commensal suctorian Choanophrya infundibulifera have been examined by light, scanning and transmission electron microscopy. The tentacles possess a flattened tip and rounded shaft externally, with a neck and root region internally. There is a microtubule canal consisting of 150 ring microtubules within which are 20–35 curved lamellae each containing about 20 microtubules. Novel structural features include pairs of short oblique arranged microtubules at the tip, and a collar of epiplasm in the neck region. No haptocysts are found in Choanophrya but the tentacle cytoplasm contains two types of inclusions named solenocysts and spherical vesicles. These features are discussed in relation to the processes of tentacle movement and feeding. The rapid longitudinal movements of the tentacles are described and compared to those of other suctorians and possible mechanisms are suggested. Ingestion in Choanophrya is described and several theories involving tentacle microtubules in the feeding process are examined.This investigation was supported by the J.S. Dunkerley Fellowship in Protozoology, awarded by the University of Manchester.     

First in situ observations of the deep-sea squid Grimalditeuthis bonplandi reveal unique use of tentacles

The deep-sea squid Grimalditeuthis bonplandi has tentacles unique among known squids. The elastic stalk is extremely thin and fragile, whereas the clubs bear no suckers, hooks or photophores. It is unknown whether and how these tentacles are used in prey capture and handling. We present, to our knowledge, the first in situ observations of this species obtained by remotely operated vehicles (ROVs) in the Atlantic and North Pacific. Unexpectedly, G. bonplandi is unable to rapidly extend and retract the tentacle stalk as do other squids, but instead manoeuvres the tentacles by undulation and flapping of the clubs’ trabecular protective membranes. These tentacle club movements superficially resemble the movements of small marine organisms and suggest the possibility that G. bonplandi uses aggressive mimicry by the tentacle clubs to lure prey, which we find to consist of crustaceans and cephalopods. In the darkness of the meso- and bathypelagic zones the flapping and undulatory movements of the tentacle may: (i) stimulate bioluminescence in the surrounding water, (ii) create low-frequency vibrations and/or (iii) produce a hydrodynamic wake. Potential prey of G. bonplandi may be attracted to one or more of these as signals. This singular use of the tentacle adds to the diverse foraging and feeding strategies known in deep-sea cephalopods.     

FINE STRUCTURE AND CYTOCHEMISTRY OF LILIUM POLLEN TUBES

Growth of the Lilium longiflorum pollen tube in vitro is restricted to a zone extending back 3–5 μ from the tip. Electron micrographs of cross and longitudinal thin sections of L. longiflorum and L. regale pollen tubes reveal that the cytoplasm of the nongrowing region of the tube contains an abundance of mitochondria, amyloplasts, Golgi bodies, endoplasmic reticulum, lipid bodies, and vesicles. In contrast, the growing tip is characterized by an abundance of vesicles and an absence of other cytoplasmic elements. The vesicles appear to be of 2 types. One is spherical, about 0.1 μ in diameter, stains strongly with phosphotungstic acid, apparently arises from the Golgi apparatus and appears to contribute to tube wall and plasmalemma formation. The other type is irregular in shape, 0.01-0.05 μ in diameter, stains strongly with lead hydroxide, and is of unknown origin and function. Cytochemical analysis indicates that the tips of L. longiflorum pollen tubes are singularly rich in ribonucleic acid, protein, and carbohydrate. These findings are discussed in relation to tube growth.     

An Electron Microscope Study of the Contractile Vacuole in Tokophrya infusionum

Contractile vacuoles are organelles that collect fluid from the cytoplasm and expel it to the outside. After each discharge (systole), they appear again and expand (diastole). They are widely distributed among Protozoa, and have been found also in some fresh water algae, sponges, and recently in some blood cells of the frog, guinea pig, and man. In spite of the extensive work on the contractile vacuole, very little is known concerning its mode of operation. An electron microscope study of a suctorian Tokophrya infusionum provided an opportunity to study thin sections of contractile vacuoles, and in these some structures were found which could be part of a mechanism for the systolic and diastolic motions the organelle displays. In Tokophrya, as in Suctoria and Ciliata in general, the contractile vacuole has a permanent canal connecting it with the outside. The canal appears to have a very elaborate structure and is composed of three parts: (1) a pore; (2) a channel; and (3) a narrow tubule located in a papilla protruding into the cavity of the contractile vacuole. Whereas the pore and channel have fixed dimensions and are permanently widely open, the tubule has a changeable diameter. At diastole it is so narrow (about 25 to 30 mµ in diameter) that it could be regarded as closed, while at systole it is widely open. It is assumed that the change in diameter is due to the contraction of numerous fine fibrils (about 180 A thick) which are radially disposed around the canal in form of a truncated cone, with its tip at the channel, and its base at the vacuolar membrane. It seems most probable that the broadening of the tubule results in discharge of the content of the contractile vacuole. In the vicinity of the very thin limiting vacuolar membrane, small vesicles and canaliculi of the endoplasmic reticulum, very small dense particles, and mitochondria may be found. In addition, rows of closely packed vesicles are present in this region, and in other parts of the cytoplasm. It is suggested that they might represent dictyosome-like bodies, responsible for withdrawing fluids from the cytoplasm and then conveying them to the contractile vacuole, contributing to its expansion at diastole.     

Ecology and behaviour of a free-swimming tube-dwelling rotifer Cephalodellaforficula

SUMMARY. 1. Cephalodella for ficula (Ploima, Rotifera) lives in tubes it constructs itself. These tubes are built of mueus in detritus-rich environments. The tubes are often closed at both ends, arc not used as sieves, and are not eaten directly.
2. The rotifer swims back and forth in its tube and apparently lives on bacteria which are shed from the inner walls of the tubes. Because of surface-to-volume considerations, this feeding strategy is probably only possible for animals smaller than roughly 1 mm. Under low food conditions, rotifers inside a tube have a distinctly higher fitness than rotifers removed from their tube.
3. Given high food conditions, rotifers removed from a tube immediately build another. Grazing on particles outside the tube appears to take place when a tube is being lengthened. Rotifers do not leave the tube for routine feeding, but under conditions of starvation or very low oxygen concentration they will leave the tube and swim about.     

Comparative ultrastructure of catch tentacles and feeding tentacles in the sea anemone Haliplanella

TEM observations of catch tentacles revealed that the tentacle tip epidermis is filled with two size classes of mature holotrich nematocysts and a gland cell filled with electron-dense vesicles. Vesicle production is restricted to upper-middle and tentacle tip regions, whereas holotrich development occurs in the lower-middle and tentacle base regions. Thus, catch tentacles have a maturity gradient along their length, with mature tissues concentrated at the tentacle tip. Occasional feeding tentacle cnidae (microbasic p-mastigophores and basitrichs) and mucus gland cells occur in proximal portions of catch tentacles, but are phagocytized by amoeboid granulocytes and transported to the gastrodermis for further degradation. No feeding tentacle cnidae or mucus cells occur distally in catch tentacles. Unlike catch tentacles, feeding tentacles are homogeneous in structure along their length with enidocytes containing mature spirocysts, microbasic p-mastigophore or basitrich nematocysts distributed along the epithelial surface. Cnidoblasts are recessed beneath cnidocytes, occurring along the nerve plexus. Mucus gland cells and gland cells filled with electron-dense vesicles are present in feeding tentacles, distributed at the epithelial surface. Granular phagocytes are rare in the feeding tentacle tip, but common in the tentacle base.     

Ultrastructural Localization of Acid Phosphatase in Starved Tokophrya infusionum*

SYNOPSIS. Young organisms of Tokophrya infusionum starved for several hr, are best suited for a study of the fine structure of this organism including the distribution of its organelles. Acid phosphatase was localized by a combined electron microscopy and cytochemical approach using modified Gomori methods. The enzyme was found in small dense bodies, spheroid vesicles, missile-like bodies, rough-surfaced endoplasmic reticulum, residue and autophagic vacuoles. The small dense bodies are thought to be primary lysosomes since electron micrographs show a) a continuity between the membrane of the rough-surfaced endoplasmic reticulum and that of the dense bodies and b) a connection between the contents of both structures when the dense bodies form from the endoplasmic reticulum.