Ontogeny of the uredium of Melampsora lini

1979 ◽  
Vol 57 (6) ◽  
pp. 639-649 ◽  
Author(s):  
Z. M. Hassan ◽  
L. J. Littlefield

Light microscopy and transmission and scanning electron microscopy were used to study the development of uredia of Melampsora lini. Uredia were produced 6–10 days after inoculation with urediospores of M. lini. Uredium ontogeny began with the formation of a uredium initial from a hyphal plexus in a substomatal cavity. The hyphae oriented vertically and expanded; the enlarged ends divided to form a palisade of uredial initial cells. These cells divided into basal and terminal cells. Each terminal cell divided transversely to form a peridial and an intercalary cell; the basal cell became the sporogenous cell. The intercalary cells disintegrated early in the expansion of the uredium and released their contents into the intercellular matrix. The sporogenous cell, usually swollen at one end, gave rise by budding to successive sympodially produced spore buds which elongated and divided transversely to form pedicels and immature spore cells. As the spores matured the pedicels shriveled and became separated from the urediospores. Elongated, often capitate, paraphyses formed throughout the uredium and functioned to rupture the peridium and epidermis which covered the immature uredium. The peridium and the intercalary cells formed only once during ontogeny of the uredium, this being associated with only the first generation of urediospores. The intercalary cells were disrupted during uredium ontogeny, and most of the peridial cell layer was sloughed off, along with the overlying epidermis, upon rupture of the latter. The paraphyses were permanent and remained in the uredium throughout its functional life. Successive generations of urediospores arose within the same uredium from spore buds produced sympodially from the original sporogenous cell but without forming additional peridial or intercalary cells.

2014 ◽  
Vol 20 (6) ◽  
pp. 1625-1637 ◽  
Author(s):  
Catalina Mansilla ◽  
Václav Ocelík ◽  
Jeff T. M. De Hosson

AbstractThis paper presents a statistical method to analyze instabilities that can be introduced during imaging in scanning electron microscopy (SEM). The method is based on the correlation of digital images and it can be used at different length scales. It consists of the evaluation of three different approaches with four parameters in total. The methodology is exemplified with a specific case of internal stress measurements where ion milling and SEM imaging are combined with digital image correlation. It is concluded that before these measurements it is important to test the SEM column to ensure the minimization and randomization of the imaging instabilities. The method has been applied onto three different field emission gun SEMs (Philips XL30, Tescan Lyra, FEI Helios 650) that represent three successive generations of SEMs. Important to note that the imaging instability can be quantified and its source can be identified.


1987 ◽  
Vol 65 (1) ◽  
pp. 124-130 ◽  
Author(s):  
James A. Traquair ◽  
Denis A. Gaudet ◽  
Eric G. Kokko

The effects of temperature on the production of sclerotia by the snow mold basidiomycete, Coprinus psychromorbidus, are described for the first time. Numbers of sclerotia produced and the optimum temperature for sclerotium production were variable for isolates observed. In general, the influence of temperature on sclerotium production was independent of its influence on colony growth. Optimal temperatures for production of sclerotia were higher than those for radial growth of colonies. Scanning electron microscopy revealed a centripetal pattern of differentiation in developing sclerotia. Distinctive rind, cortex, and medulla were evident after 8 to 10 weeks. Rind and cortex were multilayered. Thick-walled cells were cemented together by an amorphous intercellular matrix. Melanin was located in the rind cell walls for the first time by scanning electron microscopy and backscattered electron imaging of silver-stained sections. With the transmission electron microscope, melanin granules were observed only in the intercellular matrix and outer layers of rind cell walls. Inflated medullary cells were predominantly thin walled and contained vacuolate cytoplasm.


Author(s):  
Kan Kobayashi

It is known that some kinds of dendritic cells are distributed in the epithelial cell layer of mucous membrane consisting of stratified squamous epithelium. In the process of exfoliation of the epithelial layer from the underlying connective tissue, dendritic cell bodies exposed on the ruptured surface of the epithelium were detected by scanning electron microscopy. These cells were also observed by light microscopy as well as by transmission electron microscopy.Dorsal mucous membrane of the ox tongue was fixed in Karnovsky's fixative or in 10% formalin. For scanning electron microscopy samples were immersed in 3N-HCl solution for 2-3 weeks at room temperature. The epithelial cell layer was removed from the underlying connective tissue layer1). They were postfixed in tannic acid and then 1% OsO4 for 1 hr. After dehydration in an ethanol series, the specimens were dried by passing through t-butylalcohol, coated with platinum-palladium and observed under an S-800 scanning electron microscope. For transmission electron microscopy, small pieces of the fixed tissue were post-fixed in 1% OsO4 for 1.5 hr and then embedded in Araldite-Epon.


Zootaxa ◽  
2010 ◽  
Vol 2495 (1) ◽  
pp. 53 ◽  
Author(s):  
VALERIA C. ONOFRIO ◽  
MARCELO B. LABRUNA ◽  
JOÃO LUIZ H. FACCINI ◽  
DARCI M. BARROS-BATTESTI

The tick Ixodes luciae occurs in many countries within the Neotropical region but only adult ticks have been morphologically described. Larvae and nymphs parasitize marsupials and rodents while adults are common on marsupials. A colony of I. luciae was obtained from females collected on marsupials from the State of Rondônia, Northern Brazil. After being fed on rabbits, the specimens were maintained under controlled conditions of temperature and humidity. Unfed larvae, nymphs, males and females of the first generation were cleaned and prepared for both optical and scanning electron microscopy. Ixodes luciae is closely related to Ixodes loricatus, Ixodes schulzei, and Ixodes amarali, although each species has its own array of distinctive characters. The larva of I. luciae differs from those of both I. schulzei and I. amarali in the length of the capitulum and from I. schulzei in the number of posthalleral setae in the Haller’s organ. Nymphs differ from I. amarali, I. loricatus and I. schulzei by the length of the external spur on coxae I, and from I. schulzei and I. amarali in having slender and shorter capitulum and hypostome. Males and females of I. luciae differ from the other three species by the length of the external spur on coxae I and by the scutal punctations, which are much longer and larger, respectively, in I. luciae. However, except for a few features, the chaetotaxy is the same for larvae of the four species, not only on the idiosoma (e.g. scutum with four pairs of setae), palpi and tarsus I, but also the number of porose setae within the capsule of Haller’s organ and the prehalleral setae.


2002 ◽  
Vol 27 ◽  
pp. 15-25 ◽  
Author(s):  
Mª Ángeles Martín Mosquero ◽  
Rocío Juan ◽  
Julio Pastor

RESUMEN. Estudio morfológico)' anatómico en miculas de Nepeta L. (Lamiaceae) del suroeste de España. Se describe la micromorfología y la anatomía de las núculas en las cinco especies de Nepeta L. presentes en el suroeste de España: N. catana L., N. amethystina var. anticaria Ladero & Rivas Goday, N. multibracteata Desf., N. tuberosa L. subsp. tuberosa y N. apuleii Ucria, tanto al microscopio óptico (M.O.) como al microscopio electrónico de barrido (M.E.B.). Los resultados han permitido diferenciar tres tipos estructurales atendiendo básicamente a la ornamentación de la núcula. Además, los caracteres anatómicos han permitido delimitar los taxones estudiados fundamentalmente a nivel del epicarpo, mesocarpo y capa en empalizada. La excreción de mucílago en las núculas de N. amethystina var. anticaria ha permitido diferenciar claramente este taxón. Así mismo, atendiendo a los caracteres carpológicos estudiados, se propone una clave para diferenciar los citados taxones.Palabras clave. Núcula, morfología, anatomía, mucílago, Nepeta, Lamioideae.ABSTRACT. Morphological and anatomical studies on nutlets of Nepeta L. (Lamiaceae) from South-West Spain. The micromorphology and anatomy of nutlets of the five Nepeta L. species from South-West Spain: N. ca/aria L., N. amethystina var. anticaria Ladero & Rivas Goday, N. multibracteata Desf., N. tuberosa L. subsp. tuberosa y N. apuleii Ucria, are described with light and scanning electron microscopy. The results have showed the possibility to differentiate three structural nutlet types basically attending of nutlet ornamentation. Anatomical characters have allowed distinguish the examined taxa using epicarp, mesocarp and sclerenchymatic cell layer characters. The mucilage secretion of N. atnethystina var. anticaria nutlet has allowed easily define this taxon. Also, a key to differentiate the five taxa using carpological characters is provided.Key words. Nutlet, morphology, anatomy, mucilage, Nepeta, Lamioideae.


1979 ◽  
Vol 57 (6) ◽  
pp. 629-638 ◽  
Author(s):  
R. E. Gold ◽  
L. J. Littlefield

Urediospore infection by Melampsore lini on stems or leaves of Linum usitatissimum produced uredia which quickly converted from urediospore to teliospore production. The telium was composed of a palisade of laterally united, sessile, prismatic teliospores (ca. 50 × 6 μm) positioned between the epidermis and the stem cortex. Teliospores were induced to germinate by subjecting telia to a series of freeze–thaw and wet–dry cycles. Germination began after 6–10 such cycles and continued until 20–24 cycles had been performed. Teliospores germinated apically to form basidia and smooth, ovate to elliptical basidiospores (ca. 6 × 5 μm). Basidiospore germlings penetrated directly through the host epidermis and formed intercellular and intracellular hyphae. The haploid intracellular structures formed were irregular and hypha like, often septate, and occasionally grew into adjacent host cells. Several morphological variants of intracellular hyphae were observed; all such structures were distinct from the more specialized dikaryotic haustoria derived from either dikaryotic aeciospore or urediospore infections. Development of pycnia occurred primarily in the substomatal cavities of leaves. Flexuous hyphae extended through stomata; concomitantly, pycniospores produced in chains from a palisade of pycniosporophores exuded through the stomata onto the leaf surface in droplets of honeydew. Pycniospores were smooth, ellipsoidal, and ca. 3 × 1.5 μm. Caeomoid aecia developed on both sides of flax leaves and on stems. Short irregular chains of aeciospores alternating with smaller wedge-shaped intercalary cells were produced from sporogenous hyphae at the base of aecia. Mature aeciospores were globose to ovate (ca. 16 × 13 μm) and were densely ornamented with smooth, cog-like verrucae.


Author(s):  
P.S. Porter ◽  
T. Aoyagi ◽  
R. Matta

Using standard techniques of scanning electron microscopy (SEM), over 1000 human hair defects have been studied. In several of the defects, the pathogenesis of the abnormality has been clarified using these techniques. It is the purpose of this paper to present several distinct morphologic abnormalities of hair and to discuss their pathogenesis as elucidated through techniques of scanning electron microscopy.


Author(s):  
Charles TurnbiLL ◽  
Delbert E. Philpott

The advent of the scanning electron microscope (SCEM) has renewed interest in preparing specimens by avoiding the forces of surface tension. The present method of freeze drying by Boyde and Barger (1969) and Small and Marszalek (1969) does prevent surface tension but ice crystal formation and time required for pumping out the specimen to dryness has discouraged us. We believe an attractive alternative to freeze drying is the critical point method originated by Anderson (1951; for electron microscopy. He avoided surface tension effects during drying by first exchanging the specimen water with alcohol, amy L acetate and then with carbon dioxide. He then selected a specific temperature (36.5°C) and pressure (72 Atm.) at which carbon dioxide would pass from the liquid to the gaseous phase without the effect of surface tension This combination of temperature and, pressure is known as the "critical point" of the Liquid.


Author(s):  
P.J. Dailey

The structure of insect salivary glands has been extensively investigated during the past decade; however, none have attempted scanning electron microscopy (SEM) in ultrastructural examinations of these secretory organs. This study correlates fine structure by means of SEM cryofractography with that of thin-sectioned epoxy embedded material observed by means of transmission electron microscopy (TEM).Salivary glands of Gromphadorhina portentosa were excised and immediately submerged in cold (4°C) paraformaldehyde-glutaraldehyde fixative1 for 2 hr, washed and post-fixed in 1 per cent 0s04 in phosphosphate buffer (4°C for 2 hr). After ethanolic dehydration half of the samples were embedded in Epon 812 for TEM and half cryofractured and subsequently critical point dried for SEM. Dried specimens were mounted on aluminum stubs and coated with approximately 150 Å of gold in a cold sputtering apparatus.Figure 1 shows a cryofractured plane through a salivary acinus revealing topographical relief of secretory vesicles.


Author(s):  
Nakazo Watari ◽  
Yasuaki Hotta ◽  
Yoshio Mabuchi

It is very useful if we can observe the identical cell elements within the same sections by light microscopy (LM), transmission electron microscopy (TEM) and/or scanning electron microscopy (SEM) sequentially, because, the cell fine structure can not be indicated by LM, while the color is; on the other hand, the cell fine structure can be very easily observed by EM, although its color properties may not. However, there is one problem in that LM requires thick sections of over 1 μm, while EM needs very thin sections of under 100 nm. Recently, we have developed a new method to observe the same cell elements within the same plastic sections using both light and transmission (conventional or high-voltage) electron microscopes.In this paper, we have developed two new observation methods for the identical cell elements within the same sections, both plastic-embedded and paraffin-embedded, using light microscopy, transmission electron microscopy and/or scanning electron microscopy (Fig. 1).


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