The Test Structure and Composition of the Foraminifer Rosalina floridana*

SYNOPSIS. The composition of the test of Rosalina floridana (Cushman) was examined histochemically, and its structure was studied with the electron microscope by means of thin sections and carbon replicas. The test is composed of a thick organic lining overlain by one or more calcite layers bounded above and below by thin membranes. The membranes are fused to organic pore processes composed of coarse fibers that penetrate the calcite layers. The ***lining, consisting of coarse fibers matted into a laminated sheet, is considered a strengthening element of the test. The membranes covering each calcite layer are composed of fine, headed fibrils which in aggregate have a striated pattern; they are thought to be the crystal-nucleating agent during calcification and to form a protective covering for the previously deposited calcite layers. The pore processes, which are devoid of an internal entrance for cytoplasm, are considered to be points of attachment for the membranes; they tie the organic test components into a unified whole. The calcite layers and the chambers lack this unity, being separated from each other and from the preceding chambers by membranes so that there are no calcite-to-calcite boundaries between them. An organic, sievelike structure of undetermined function has been found in the foramina of chambers near the prolocular region of the test. Histochemical methods show that the lining contains proteins, polysaccharides, and unidentified substances; the membranes and the pore processes stain as a protein-polysaccharide complex free of other substances.     

Observations on Iridia diaphana, a Marine Foraminifer

SYNOPSIS. Iridia diaphana , a marine foraminifer, was used as a subject for observations on grano-reticulate pseudopods. The organism readily forms a pseudopod net and its behavior is roughly predictable. Test composition varies with the environment; test shape is more constant. Pseudopod form and structure were observed by transmitted plane and polarized light microscopy, by freeze-drying and scanning electron microscopy, and by thin section studies in the transmission electron microscope. Rigidity is probably due to the numerous 250 A dia. microtubules in the pseudopods. Other organelles observed include mitochondria, vesicles and vacuoles. The plasmalemma may have numerous villous projections. Pseudopod form in I. diaphana does not closely resemble that of Allogromia laticollaris as reported by Wohlfarth-Bottermann (25). A pseudopod may be composed of several membrane-bound units of cytoplasm, or of a single unit of cytoplasm. A reassessment of the theories of the mechanism of cytoplasmic streaming in foraminiferan pseudopods is necessary.     

Observations on Some Internal Structures and Pseudopods of Lesquereusia spiralis (Rhizopoda, Testacida)

SYNOPSIS. The internal structure and activities of Lesquereusia spiralis was observed by the use of nonmotile individuals which had incorporated a cover glass as part of their shell. As many as 14 ectoplasmic strands or epipods connect the main cytoplasmic mass to the inner surface of the shell. Two to 14 contractile vacuoles 2–5 μ in diameter at 22–25 C were present. A few epipods contained contractile vacuoles. The vacuoles emptied every 1–2 min. Both the number of epipods and contractile vacuoles varied with the degree of pseudopod activity; the more active the pseudopods, the more numerous these organelles. Egestion of indigestible food residues from the cytoplasm takes place just beyond the mouth of the shell thru vacuoles about 15 μ in diameter. Frequently, long flattened pseudopods of a tensile or contracting type were formed. In some cases pseudopods of this type were seen to pull themselves in 2 when the distal end remained attached and contraction continued.     

Ultrastructural study of in vitro larval development of Echinococcus granulosus protoscoleces

Through ultrastructural study of the morphological forms developed in vitro during protoscolex culture, we describe larval E. granulosus histogenesis. The transformation of the spined microtriches in the protoscolex into truncated microtriches that develop within the hydatid cyst is discussed. The paper also describes the mitochondria location change that occurs during the evolution; the mitochondria pass from the most internal area of the distal cytoplasm along the cytoplasmic extensions into the cytoplasm of tegumental cells. The ultrastructures of both the vesiculated protoscolex and the posterior bladder demonstrate that each state corresponds to the initial step on one of the two paths of in vitro vesicular development.     

Ultrastructural Changes During Encystment of Schizopyrenus russelli*

Ultrastructural changes associated with the encystment of Schizopyrenus russelli have been studied by electron microscopy. Before encystment small “black bodies” appear in the cytoplasm and later migrate toward the periphery. The outer cyst wall is secreted at this stage as a thin discontinuous layer which thickens and subsequently becomes continuous. Concomitant with this, the endoplasmic reticulum surrounds the mitochondria. The inner cyst wall later appears as a multilayered structure which presumably is cast off from the plasma membrane. Between the inner and outer layers of the cyst wall, there is a middle, less electron-dense layer wherein extruded cytoplasmic material is found embedded at certain places.     

Encystment and Excystment of the Heterotrichous Ciliate Blepharisma stoltei Isquith*

SYNOPSIS. The structure and cytochemistry of encystment and excystment of Blepharisma stoltei Isquith are described. The encystment process may be subdivided into 4 stages: (i) in the precystic stage the buccal apparatus overlaps about the posterior, (ii) in early encystment, the buccal apparatus is resorbed and an ectocyst is secreted, (iii) an interwall space, endocyst, and plug are secreted during late encystment, and (iv) the resting cyst stage typically has disc-like structures on the ectocyst, and a vacuole in the macronucleus. In excystment, 6 distinct stages may be defined: (i) partial kineties are formed in early excystment, (ii) permanent kineties give rise to anlagen of the buccal apparatus during stomatogenesis, (iii) the organism elongates and reforms the vegetative shape in late excystment, (iv) some cysts then divide, (v) the redeveloped organism is liberated thru the plug pore, and (vi) the postcystic stage resembles the vegetative form except for its size and lack of pigmentation. Cortical structures, extracellular membranes, and the macronuclear membrane are composed of protein-lipids. Unbound protein and RNA are found in the cytoplasm thruout the cystic cycle. DNA is present only in the nuclei. Polysaccharides, 1st found in the cytoplasm, are shifted to the plug in encystment. The plug material disappears during excystment, while PAS positive granules appear in the cytoplasm.     

ALGAL CALCIFICATION IN SOME CODIACEAE (CHLOROPHYTA): ULTRASTRUCTURE AND LOCATION OF SKELETAL DEPOSITS1,2

The capitular filaments of Penicillus and Rhipocephalus consist of an inner tube containing the cytoplasm and an outer calcified sheath. The sheath originates at the cell wall and differentiates into several layers which form the outer filament wall. CaCO₃ is deposited between organic layers within the sheath and is not in direct contact with the seawater. Pores within the sheath, usually uncalcified, may facilitate exchange of gases and solutes. The cytoplasm is characterized by vacuolar inclusions of calcium oxalate needles 50–150 μm long. A closed cortical surface is lacking. Udotea cyathiformis Dec. and U. conglutinata (Ellis & Sol.) Lam. are similar to Penicillus and Rhipocephalus, in addition showing some CaCO₃ between filaments (ICS-calcification). Udotea flabellum (Ellis & Sol.) Lam. is different as the filaments are profusely branched giving rise to a fully developed cortical surface. Pores and vacuolar calcium oxalate inclusions are absent. CaCO₃ deposition occurs within cortical filaments in between layers of the filament wall and subcortically in intercellular spares (ICS). Cortex calcification shows primary and secondary deposits bearing some resemblance to sheath calcification and to coralline red algae. In Rhipocephalus phoenix (Ellis & Sol.) Kütz., Penicillus pyriformis A. &E. Gepp, U. cyathiformis and U. conglutinata CaCO₃ is precipitated intracellularly within the sheath, in contrast to Halimeda and Cymopolia where it is deposited extracellularly in between filaments. U. flabellum takes an intermediate position showing both intra- and intercellular calcification. The sheath compartment volume is between 12.5 and 7500 μm³and 5–3 orders of magnitude smaller than the ICS-compartment. Compartment size and location of CaCO₃may bear on calcification mechanisms. One condition for such a mechanism may be restricted exchange of solutes (CO₂, CO₃^2-, HCO₃^-, O₂, Co²⁺). Codiaceae; filament ultrastructure; Penicillus; Rhipocephalus; Udotea     

Ultrastructural study of the mature egg of Tethya citrina sarà and melone (porifera,demospongiae)

Tethya citrina is an oviparous demosponge in which eggs are distributed in clumps within the choanosome. The cytoplasm of the mature egg presents a peripheral cortex consisting of a slightly granular layer sandwiched between two densely granular, vesiculated ones. The cortex probably has a specialized, trophic function. Mesohyl bacteria are phagocyted at the egg surface, included in vacuoles, and transferred across the cortical sheath toward the inner cytoplasm. The region of the egg extending between the cortex and the nucleus shows a lacunary system mostly developed beneath the cortical envelope. The noncortical cytoplasm also contains lipid droplets, dense rodlike bodies, and phagosomelike granules. Most of the latter are probably autophagosomes, forming lacunae and supporting autosynthetic vitellogenesis. Rodlike inclusions are probably proteinaceous; they likely originate within the phagosomes and represent the actual yolk material.     

Salt‐inducible kinase induces cytoplasmic histone deacetylase 4 to promote vascular calcification

A pathologic osteochondrogenic differentiation of vascular smooth muscle cells (VSMCs) promotes arterial calcifications, a process associated with significant morbidity and mortality. The molecular pathways promoting this pathology are not completely understood. We studied VSMCs, mouse aortic rings, and human aortic valves and showed here that histone deacetylase 4 (HDAC4) is upregulated early in the calcification process. Gain‐ and loss‐of‐function assays demonstrate that HDAC4 is a positive regulator driving this pathology. HDAC4 can shuttle between the nucleus and cytoplasm, but in VSMCs, the cytoplasmic rather than the nuclear activity of HDAC4 promotes calcification, and a nuclear‐localized mutant of HDAC4 fails to promote calcification. The cytoplasmic location and function of HDAC4 is controlled by the activity of salt‐inducible kinase (SIK). Pharmacologic inhibition of SIK sends HDAC4 to the nucleus and inhibits the calcification process in VSMCs, aortic rings, and in vivo. In the cytoplasm, HDAC4 binds and its activity depends on the adaptor protein ENIGMA (Pdlim7) to promote vascular calcification. These results establish a cytoplasmic role for HDAC4 and identify HDAC4, SIK, and ENIGMA as mediators of vascular calcification.     

Fine Structure of the Macronuclear Anlage of the Hypotrichous Ciliate Keronopsis rubra

In exconjugants of the hypotrich Keronopsis a large, highly polyploid macronuclear anlage is formed from which condensed chromatin bodies are passed into the cytoplasm where they are thought to give rise to the numerous small macronuclei of the vegetative cell. Electron microscopy shows that the chromatin bodies within the macronuclear anlage are separated from each other by sheets of low contrast lamellar material. The anlage appears therefore as a composite nucleus containing prepacked units which are extruded into the cytoplasm following condensation.     

Rapid intracellular motility and dynamic membrane events in an Antarctic foraminifer

Some properties of cytoplasmic transport in a cold-adapted (Antarctic) organism are reported for the first time. Phase-contrast light microscopy of Astrammina rara, an arenaceous foraminiferan protozoan, reveals that the saltatory transport of cytoplasmic granules in reticulopods occurs bidirectionally and at rates up to 7.5-micron/s. Extracellularly attached latex microspheres are rapidly translocated on the reticulopodial surface, thus demonstrating membrane fluidity at low (-1.8 degrees C) ambient temperatures. Rapid extension/withdrawal and branching/fusing of pseudopodia further illustrate dynamic plasma membrane activity at subzero temperatures. Immunofluorescence microscopy with an antibody monospecific for tubulin shows that these pseudopods contain microtubules. The motility of this cold-adapted foraminifer therefore appears fully comparable to the motility of allogromiid foraminifers from temperate waters.     

The genusGeitleria (Cyanophyceae orCyanobacteria): Distribution ofG. calcarea andG. floridana n. sp.

The calcifying cave inhabitant atmophytic blue-green algaGeitleria calcarea is reported from new localities in Florida and in the Cook Islands.—G. floridana n. sp., is described from caves in Florida. The calcified sheath has the shape of a quadratic prism and is built of crystalline acicular subunits about 0.1 µm in diameter. The subunits mostly form a rhombic lattice pattern but in some cases, they are not distinguishable and then the surface of the sheath is smooth.This paper is dedicated with gratitude to my former teacher, Prof. Dr.Lothar Geitler, for his 80th birthday.     

Response to chilling stress in plant cells I. Changes in cyclosis and cytoplasmic structure

Summary Cytoplasmic structure and rates of cyclosis in trichomes from chilling-sensitive watermelon (Citrullus vulgaris L.), tomato (Lycopersicon esculentum Mill.) andEpiscia reptans plants and from chilling-resistant foxglove (Digitalis purpurea) andVeronica persica were examined with differential interference contrast optics (DIC) as the temperature of the microscope stage was lowered. Below the chilling threshold, the rate of streaming in chilling-sensitive species fell markedly. At chilling temperatures the complex network of transvacuolar strands in the cytoplasm disappeared and the cytoplasm became vesiculated. During rewarming of the chilled cells, the vesicles fused into pleiomorphic blebs, which gradually stretched out into fully functional strands. These events were not seen during the chilling and rewarming of chilling-resistant plant cells.Similar inhibition of cyclosis and changes in cytoplasmic structure were observed in cells from all species studied when they were treated with the actin inhibitor, cytochalasin B, or with uncoupling agents. Phalloidin had no detectable effect. Cyclosis in colchicine-, nocodazole-, trifluralin- and IPC-treated cells was not affected for many hours and did not cause the structural changes seen with chilling. The possible role of actin in these low-temperature effects on cytoplasmic structure and function is discussed.     

Reconstitution of the Golgi reassembly process in semi-intact MDCK cells

The Golgi apparatus, which consists of stacks of cisternae during interphase, is fragmented or dispersed throughout the cytoplasm at the onset of mitosis. A sea sponge metabolite, ilimaquinone (IQ), causes Golgi membranes to vesiculate. And after its removal, the vesiculated membranes reassemble into stacks of cisternae in the perinuclear region. To study the mechanism of Golgi membrane dynamics during mitosis, we have reconstituted the reassembly process of IQ-induced vesiculated Golgi membranes in streptolysin O-permeabilized Mardin-Darby canine kidney (MDCK) cells. Monitoring the dynamics of Golgi membranes labeled with a green fluorescence protein (GFP)-tagged protein, we dissected the process into two elementary components: the reassembly of vesiculated Golgi membranes into punctate structures; and the subsequent reformation of these structures into stacks of cisternae near the nucleus. Using morphometric analysis, we studied the kinetics and biochemical requirements for the process, and revealed that an NEM-sensitive factor, cytoplasmic dynein, and GTP binding protein were involved in the Golgi reassembly.     

Gametogenesis in the Monothalamous Agglutinated Foraminifer Cribrothalammina alba

Gametogenesis in the foraminifer Cribrothalammina alba involves changes in both the gamontic test and cytoplasm. As gametes begin to differentiate and gametic flagella emerge, pores form in a regular array over the gamontic test, constituting the only avenue for gamete release. The spherical, biflagellated gametes average 1.5μ in diameter and are released in rapidly moving swarms along with flagellated “spherical masses” that probably result from incomplete gametic differentiation. Gametogenesis occurs entirely within the test and utilizes the entire cytoplast. After gamete release is complete, the agglutinated test collapses and disaggregates within a fairly short time. Similar modifications of the gamontic test occur during gametogenesis in Ovammina opaca Dahlgren, but are otherwise unknown among monothalamous agglutinated foraminifera at present.     

Phagotrophy and development ofPaulsenella cf.chaetoceratis (Dinophyta), an ectoparasite of the diatomStreptotheca thamesis

Zoospores of the dinophytePaulsenella cf.chaetoceratis, parasitizing the marine diatomStreptotheca thamesis, attach to the girdle region of the host and drive a peduncle into the cell interior. The peduncle consists of a non-cytoplasmic crook, a cytoplasmic feeding tube, and a presumably cellulosic sheath around the proximal part of the feeding tube. The crook seems to be used for attachment and penetration of the host. The mobile feeding tube induces shrinkage of the host vacuoles and takes up the complete host cytoplasm within less than 1 h. Phagocytosis depends on an intact host plasmalemma, which is not penetrated by the feeding tube. The trophic phase ends with retraction of the feeding tube. While the food is digested within a large vacuole, the trophont transforms into a thick-walled primary cyst. After about 12 h the primary cyst divides to form 3 or 4 secondary cysts. Finally, about 24 h after attacking the host, each secondary cyst releases two zoospores which may be again ready for infection within 1 h, without passing through any intermediate stage. The developmental times (above referred to 20 °C) are highly dependent on the temperature and can vary considerably, even between sister cells.Dedicated to Dr. Dr. h. c. P. Kornmann on his 75th birthday.     

Development of endosperm in Arabidopsis thaliana

 The process of endosperm development in Arabidopsis was studied using immunohistochemistry of tubulin/microtubules coupled with light and confocal laser scanning microscopy. Arabidopsis undergoes the nuclear type of development in which the primary endosperm nucleus resulting from double fertilization divides repeatedly without cytokinesis resulting in a syncytium lining the central cell. Development occurs as waves originating in the micropylar chamber and moving through the central chamber toward the chalazal tip. Prior to cellularization, the syncytium is organized into nuclear cytoplasmic domains (NCDs) defined by nuclear-based radial systems of microtubules. The NCDs become polarized in axes perpendicular to the central cell wall, and anticlinal walls deposited among adjacent NCDs compartmentalize the syncytium into open-ended alveoli overtopped by a crown of syncytial cytoplasm. Continued centripetal growth of the anticlinal walls is guided by adventitious phragmoplasts that form at interfaces of microtubules emanating from adjacent interphase nuclei. Polarity of the elongating alveoli is reflected in a subsequent wave of periclinal divisions that cuts off a peripheral layer of cells and displaces the alveoli centripetally into the central vacuole. This pattern of development via alveolation appears to be highly conserved; it is characteristic of nuclear endosperm development in angiosperms and is similar to ancient patterns of gametophyte development in gymnosperms. Received: 21 September 1998 / Revision accepted: 17 November 1998     

A cytological study of the ovary of Rhodnius prolixus. III. Cytoarchitecture and development of the trophic chamber

The tropharium of the telotrophic ovarioles of Rhodnius is syncytial with the nurse cell nuclei located in tortuous finger-like projections arborizing from a common cytoplasmic area, the trophic core. The nurse cell nuclei exhibit prominent nucleoli. Located adjacent to the nuclear envelope are masses of granular material both within the nucleus and adjoining cytoplasm. The cytoplasm consists primarily of ribosomes and mitochondria. The trophic core and the trophic cords that connect the core to individual oocytes characteristically possess parallel arrays of microtubules with ribosomes and mitochondria interspersed between. Surrounding the nurse tissue (germarium) is a thin layer of squamous cells comprising the inner sheath. The inner sheath is encompassed by the non-cellular tunica propria superficial to which are two external cellular sheaths. The syncytial nature of the tropharium appears to arise as a result of the fusion of many entangled nurse cell-oocyte complexes during the late fifth instar. The structural similarities, and possible homologies with the polytrophic type of ovariole is discussed.     

Morphology and ultrastructure of the gravity-sensitive leaf sheath base of the grass Echinochloa colonum L

When a flowering stalk of Echinochloa colonum is held horizontally, growth is initiated in the lower side of each leaf sheath base, restoring the inflorescence to an upright position. Changes in the gravity vector are perceived by specialised statolithcontaining tissue which is associated with each of the symmetrically-arranged vascular bundles within the leaf sheath bases. The morphological and ultrastructural features of these gravity-sensitive regions have been examined by light and electron microscopy. Each statocyte cell contains a large central vacuole with a thin lining of cytoplasm. Up to 50 spherical starch statoliths lie along the lowermost side of the cells and these sediment readily following geotropic stimulation. Statoliths are found in contact with the plasmalemma, or may be prevented from touching it by bands of microtubules. Dictyosomes and mitochondria are numerous, but endoplasmic reticulum is sparse. The nuclei tend to remain at the original apex of each cell. Statocytes of the leaf sheath base are compared and contrasted with those of the root tip.Abbreviations GMA glycol methacrylate - PAS periodic acid-Schiff's reagent - ER endoplasmic reticulum     

Cytoplasmic bridges,intercellular junctions,and individualization of germ cells during spermatogenesis in Dermatobia hominis (Diptera: Cuterebridae)

During mitotic and meiotic divisions in Dermatobia hominis spermatogenesis, the germ cells stay interlinked by cytoplasmic bridges as a result of incomplete cytokinesis. By the end of each division, cytoplasmic bridges flow to the center of the cyst, forming a complex, called the fusoma. During meiotic prophase I, spermatocytes I present desmosome-like junctions and meiotic cytoplasmic bridges. At the beginning of spermiogenesis, the fusoma moves to the future caudal end of the cyst, and at this time the early spermatids are linked by desmosome-like junctions. Throughout spermiogenesis, new and sometimes broad cytoplasmic bridges are formed among spermatids at times making them share cytoplasm. In this case the individualization of cells is assured by the presence of smooth cisternae that outline their structures. The more differentiated spermatids have in addition to narrow cytoplasmic bridges, plasmic membranes junctions. By the end of spermiogenesis, the excess cytoplasmic mass is eliminated leading to spermatid individualization. Desmosome-like junctions of spermatocytes I and early spermatids appear during the fusoma readjustment and segregations; on the other hand, plasmic membrane junctions appear in differentiating spermatids and are eliminated along with the cytoplasmic excess. These circumstances suggest that belt desmosome-like and plasmic membrane junctions are involved in the maintenance of the relative positions of male germ cells in D. hominis while they are inside the cysts. © 1996 Wiley-Liss, Inc.