Spore wall development in Sphagnum lescurii

1982 ◽  
Vol 60 (11) ◽  
pp. 2394-2409 ◽  
Author(s):  
Roy Curtiss Brown ◽  
Betty E. Lemmon ◽  
Zane B. Carothers
Keyword(s):  
Plasma Membrane ◽  
Outer Layer ◽  
Mature Spore ◽  
Outer Wall ◽  
Spore Wall ◽  
Spore Surface ◽  
Proximal Surface ◽  
Complex Development ◽  
Surface Ornamentation ◽  
Cortical System

The spore wall of Sphagnum is unique in the Bryophyta. The Sphagnum spore exine consists of two layers: an inner, lamellate layer (A layer) and a thick, homogenous, outer layer (B layer). The exine of other mosses consists of only the outermost homogenous layer and, at most, a thin ill-defined opaque layer. During development of the A-layer exine and the intine, a cortical system of evenly spaced microtubules underlies the plasma membrane. The ontogeny of the wall layers is not strictly centripetal. The A-layer exine develops evenly around the young spore immediately after cytokinesis. As the intine is deposited centripetally inside it, the homogenous B-layer exine is deposited outside the first-formed A layer. The B layer is responsible for the primary sculpturing of the spore surface. The mature spore is covered by an outermost perine, which is responsible for secondary surface ornamentation. A trilaesurate aperture develops on the proximal surface of each spore after deposition of the A layer. Ridges of the laesurae develop as a result of deposition of thick areas of intine. The ridges are eventually covered by the outer wall layers, whereas the fissure is covered only by the A layer and a very thin B-layer exine. The complex development of the trilaesurate aperture is evidence that the structure is not merely a mechanically induced "trilete mark" or "scar" resulting from compression of tetrahedrally arranged spores within a sporocyte wall.

Cell wall structures of Epicoccum nigrum (Hyphomycetes)

1973 ◽  
Vol 51 (5) ◽  
pp. 1071-1073 ◽  
Author(s):  
J. A. Brushaber ◽  
R. H. Haskins
Keyword(s):  
Cell Wall ◽  
Plasma Membrane ◽  
Outer Layer ◽  
Secondary Wall ◽  
Outer Wall ◽  
Wall Layer ◽  
Wall Material ◽  
Primary Wall ◽  
Electron Dense Material ◽  
Wall Structures

Two structurally distinct types of secondary wall layers are present in older hyphae in addition to the primary wall. A coarsely fibrous outer wall layer often becomes quite massive and frequently fuses with the outer wall layers of adjacent cells in the formation of hyphal strands. The uneven deposition of this outer layer often produces large verrucosities. The inner secondary wall layer is relatively electron transparent and contains a reticulum of electron-dense lines. The interface of the inner secondary wall with the cytoplasm is often very irregular, and sections of the plasma membrane are frequently overlain by wall material. The outer secondary wall of conidia is composed of an electron-dense material different from that of the outer wall of hyphae. Cells in the multicellular conidia tend to be polyhedral in shape with either very thick primary walls or thin primary walls having a thick inner wall deposit.

A systematic evaluation of basidiospore symmetry and tegumentation in hypogeous and gasteroid Russulales

1988 ◽  
Vol 66 (12) ◽  
pp. 2561-2573 ◽  
Author(s):  
Steven L. Miller
Keyword(s):  
Light Microscope ◽  
Spore Wall ◽  
Systematic Evaluation ◽  
Spore Morphology ◽  
Spore Surface ◽  
Layer 2 ◽  
Spore Walls ◽  
Poorly Differentiated ◽  
Surface Ornamentation ◽  
Dark Blue

Spore wall architecture and ontogeny of ornamentation in several genera and species of hypogeous and gasteroid Russulales are similar to those described previously for agaricoid Lactarius lignyotellus. Spore walls are composed of four layers, each differing in thickness and electron density. Layer 2 is electron transparent and corresponds to a dark blue, amyloid layer when mounted in Melzer's iodine reagent and viewed with the light microscope. Establishment of spore symmetry may be regulated by the hilar appendix body, which is a poorly differentiated cytoplasmic region in the hilar appendix of asymmetric spores of Macowanites luteolus, Elasmomyces russuloides, and Zelleromyces versicaulus but which is absent in symmetric spores of Z. sculptisporus, Martellia subochracea, and Gymnomyces yubaensis. A continuum in spore morphology from truly symmetric to asymmetric is evident in spores from individual sporocarps of many species of the Russulales. The variation in spore symmetry and spore surface ornamentation has clouded taxonomic concepts in the Russulales. Systematically, development of orthotropic and heterotropic spores has been regarded as two distinct end points of evolution, when they are likely terms describing degrees of the same phenomenon. The current circumscription of families and genera in the Russulales based on spore symmetry, therefore, appears to be artificial.

Ultrastructure of the envelopes of resistant and nonresistant Daphnia eggs

1979 ◽  
Vol 57 (9) ◽  
pp. 1773-1777 ◽  
Author(s):  
Lisa A. Seidman ◽  
John H. Larsen Jr.
Keyword(s):  
Plasma Membrane ◽  
Developmental Stage ◽  
Early Development ◽  
Outer Layer ◽  
Middle Layer ◽  
Outer Wall ◽  
Egg Envelope ◽  
Middle Component

During early development, the nonresistant egg of Daphnia had an outer wall of [Formula: see text], and an inner wall approximately the thickness of the plasma membrane. In the same genus at a comparable developmental stage, resistant eggs were surrounded by a three-layered envelope, [Formula: see text] thick. Although the outer layer [Formula: see text] of the latter appeared similar to the outer wall of the nonresistant egg, the middle layer [Formula: see text] resembled the crustacean procuticle. The outer layer developed before the formation of the middle component, and both structures were absent after development resumed. This suggests that the resistant egg envelope is characterized by an additional embryonic cuticle and molt.

Surface Structure of the Spores of Glugea Weissenbergi

1969 ◽  
Vol 27 ◽  
pp. 238-239
Author(s):  
Sanford H. Vernick ◽  
Anastasios Tousimis ◽  
Victor Sprague
Keyword(s):  
Electron Microscope ◽  
Surface Structure ◽  
Transmission Electron Microscope ◽  
Mature Spore ◽  
Spore Surface ◽  
Sectioned Material ◽  
Transmission Electron ◽  
Surface Detail

Recent electron microscope studies have greatly expanded our knowledge of the structure of the Microsporida, particularly of the developing and mature spore. Since these studies involved mainly sectioned material, they have revealed much internal detail of the spores but relatively little surface detail. This report concerns observations on the spore surface by means of the transmission electron microscope.

Ultrastructure and development of urediospore ornamentation in Melampsora lini

1971 ◽  
Vol 49 (12) ◽  
pp. 2067-2073 ◽  
Author(s):  
L. J. Littlefield ◽  
C. E. Bracker
Keyword(s):  
Endoplasmic Reticulum ◽  
Plasma Membrane ◽  
Outer Surface ◽  
Spore Wall ◽  
Wall Material ◽  
Wild Type ◽  
Melampsora Lini ◽  
Inner Surface ◽  
External Position ◽  
Basal Portion

The urediospores of Melampsora lini (Ehrenb.) Lev. are echinulate, with spines ca. 1 μ long over their surface. The spines are electron-transparent, conical projections, with their basal portion embedded in the electron-dense spore wall. The entire spore, including the spines, is covered by a wrinkled pellicle ca. 150–200 Å thick. The spore wall consists of three recognizable layers in addition to the pellicle. Spines form initially as small deposits at the inner surface of the spore wall adjacent to the plasma membrane. Endoplasmic reticulum occurs close to the plasma membrane in localized areas near the base of spines. During development, the spore wall thickens, and the spines increase in size. Centripetal growth of the wall encases the spines in the wall material. The spines progressively assume a more external position in the spore wall and finally reside at the outer surface of the wall. A mutant strain with finely verrucose spores was compared to the wild type. The warts on the surface of the mutant spores are rounded, electron-dense structures ca. 0.2–0.4 μ high, in contrast to spines of the wild type. Their initiation near the inner surface of the spore wall and their eventual placement on the outer surface of the spore are similar to that of spines. The wall is thinner in mutant spores than in wild-type spores.

Direct measurement of transverse residual strains in aorta

1996 ◽  
Vol 270 (2) ◽  
pp. H750-H759 ◽  
Author(s):  
H. C. Han ◽  
Y. C. Fung
Keyword(s):  
Stress State ◽  
Outer Layer ◽  
Residual Strain ◽  
Longitudinal Axis ◽  
Outer Wall ◽  
Residual Strains ◽  
Stress States ◽  
Sectional Surface ◽  
Thoracic And Abdominal ◽  
Load State

Residual strains were measured in the porcine aorta. Segments were cut from the aorta perpendicular to its longitudinal axis. Microdots of water-insoluble black ink were sprinkled onto the transverse sectional surface of the segments in the no-load state. The segments were then cut radially, and sectional zero-stress states were approached. The coordinates of selected microdots (2-20 microns) were digitized from photographs taken in the no-load state and the zero-stress state. Residual strains in the transverse section were calculated from the displacement of the microdots. The circumferential residual strains on the inner wall and outer wall were calculated from the circumferential lengths in the no-load state and the zero-stress state. Results show that the circumferential residual strain is negative (compressive) in the inner layer of the aortic wall and positive (tensile) in the outer layer, whereas the radial residual strain is tensile in the inner layer and compressive in the outer layer. This residual strain distribution reduces the stress concentration in the aorta under physiological load. The experimental results compared well with theoretical estimations of a cylindrical model. Regional difference of the residual strain exists and is significant (P < 0.01), e.g., the circumferential residual strains on the inner wall of the ascending, descending thoracic, and abdominal regions of the aorta are -0.133 +/- 0.019, -0.074 +/- 0.020, and -0.046 +/- 0.017 (mean +/- SD), respectively. More radial cuts of a segment produced no significant additional strains. This means that an aortic segment after one radial cut can be considered as the zero-stress state.

scholarly journals Growth and Differentiation of the Golgi Apparatus in the Red Alga, Callithamnion Roseum

1974 ◽  
Vol 14 (3) ◽  
pp. 633-655
Author(s):  
EVA KONRAD HAWKINS
Keyword(s):  
Plasma Membrane ◽  
Fine Structure ◽  
Golgi Apparatus ◽  
Red Algae ◽  
Developmental Stages ◽  
Spore Wall ◽  
Red Alga ◽  
Wall Formation ◽  
Golgi Vesicles

The fine structure of the Golgi apparatus during development of tetrasporangia of Calli-thamnion roseum is described. Dictyosomes and associated vesicles of 4 developmental stages of sporangia are examined. The wall of sporangia exhibits a heretofore unseen cuticle in red algae. Development of the spore wall and a new plasma membrane around spores occurs through fusion of adjacent Golgi vesicles along the periphery of cells. Observations are discussed in relation to wall formation and expansion of tetrads and in comparison with other work on growth and differentiation of the Golgi apparatus.

Influence of Heat Insulation Material on Thermal Stress of Long Nozzle

2012 ◽  
Vol 535-537 ◽  
pp. 1609-1614 ◽  
Author(s):  
Hui Min Liu
Keyword(s):  
Thermal Stress ◽  
Layer Thickness ◽  
Outer Layer ◽  
Heat Insulation ◽  
Outer Wall ◽  
Symmetric Model ◽  
Insulation Material ◽  
Axially Symmetric ◽  
Coefficient Of Thermal Conductivity ◽  
Heat Insulation Material

To prevent a long nozzle (LN) of non-preheating from rupture caused by thermal shock, heat insulation material (HIM) with a lower coefficient of thermal conductivity (CTC) was compounded in the inner hole (inner layer) or around the outer wall (outer layer), and the thermal stress was investigated. The two-dimension axially symmetric model of LN was proposed by simplifying the structure and boundary conditions. The influences of the HIM to the thermal stress of LN were analyzed by finite element method. The results show that the thermal stress suffered by LN can be drastically reduced by the inner layer, making the slow variation, but when its thickness increases from 2 mm to 3 mm, it almost has no influence on the thermal stress. The maximum thermal stress at the neck of LN reduces with the depression of the CTC at the inner layer thickness of 2 mm. The maximum thermal stress of LN can’t be reduced by outer layer, but the lasting time of higher stress can be shortened, and the thermal stress at the later period of steel-irrigating can be lowed. When the outer layer thickness is more than 2 mm, the increase of it has little influence on the thermal stress of LN, and the change of its CTC has little influence on the thermal stress either. The LN with tri-layer has lower thermal stress during all the period of steel-irrigating.

The fine structure and selected histochemistry of ungerminated basidiospores of Agrocybe acericola

1996 ◽  
Vol 74 (5) ◽  
pp. 780-787 ◽  
Author(s):  
Donald G. Ruch ◽  
Kiki Nurtjahja
Keyword(s):  
Fine Structure ◽  
Acid Phosphatase ◽  
Glyoxylate Cycle ◽  
Outer Wall ◽  
Spore Wall ◽  
Malate Synthase ◽  
Marker Enzyme ◽  
Wall Ultrastructure ◽  
Membrane Bound ◽  
The Glyoxylate Cycle

The basidiospore wall of Agrocybe acericola is composed of two distinct layers that are continuous around the spores. At the germ pore, the outer wall is very thin and the inner wall becomes thicker. The plasma membrane is appressed to the inner wall and lacks distinct invaginations. The protoplasm is densely packed with ribosomes. Spores contain very little lipid distributed at each end. Mitochondria are well defined and distributed throughout the cytoplasm. Spores are binucleate, with the two nuclei lying on a line nearly perpendicular to the long axis of the cell. Various sizes of single membrane-bound vacuoles are widely distributed in the cytoplasm. These vacuoles were shown to contain acid phosphatase, indicating lysosomal activity. Microbody-like organelles are observed, which are probably glyoxysomes, since assays of malate synthase, a marker enzyme of the glyoxylate cycle, are positive. Keywords: Agrocybe, spore wall ultrastructure, basidiospore ultrastructure, glyoxylate cycle, malate synthase, acid phosphatase.

A transmission electron microscopical study of the tegument of Maritrema feliui (Digenea: Microphallidae)

2013 ◽  
Vol 58 (4) ◽  
Author(s):  
Zdzisław Świderski ◽  
Isabel Montoliu ◽  
Carlos Feliu ◽  
David Gibson ◽  
Jordi Miquel
Keyword(s):  
Surface Layer ◽  
Plasma Membrane ◽  
Outer Layer ◽  
Microscopical Study ◽  
The Other ◽  
Cytoplasmic Region ◽  
Transmission Electron ◽  
Basal Plasma Membrane ◽  
Basal Plasma ◽  
Electron Microscopical

AbstractThe tegument of the microphallid digenean Maritrema feliui, examined by means of TEM, is described as a syncytial epithelium organised into two layers. The outer layer is an external anucleate, cytoplasmic region connected to a second region composed of nucleate perikarya (cytons) deeply embedded in the surrounding cortical parenchyma. The surface layer of the tegument is covered by a plasma membrane with many deep invaginations, which are apparently pinocytotic. This layer also bears numerous large, electron-dense spines of two types, which are intracellular and attached to the basal plasma membrane. Its cytoplasm is rich in free ribosomes, contains numerous mitochondria, disc-shaped granules frequently arranged in a rouleau, and several large, moderately electron-dense, membranous bodies. The subtegumentary perikarya and their nuclei, which are both flattened, are described in detail, as are their connections with the surface tegument. These perikarya appear to be the source of the disc-shaped granules and some of the other inclusions present in the surface layer. The main characteristics of the tegumental structure of M. feliui are commented upon in relation to the findings of previous publications and their suggested functions.

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