scholarly journals Histological studies on the development of Phoma root rot of alfalfa

1969 ◽  
Vol 89 (3-4) ◽  
pp. 251-262
Author(s):  
Rocío del P. Rodríguez

Several stages of the disease cycle of root rot of alfalfa caused by Phoma medicaginis var. medicaginis were studied by using scanning electron and light microscopy. First activity of the pathogen was the external colonization of the root. The pathogen penetrated directly causing discoloration and tissue disintegration. Inter- and intracellular penetration facilitated by enzymatic degradation was likely the mechanism involved in breaching the barrier of the epidermal cells. Colonization of the cortex was intercellular. Radial access to the xylem elements was achieved through the cortex. Host responses to invasion by the pathogen were suberization of cortical cell walls and occlusion of vessels with pectic substances and wound gum. Cavities in the cortex resulting from tissue degradation were associated with later stages of infection. Intracellular hyphae were observed in dead cells of the cortex and in the xylem. 

1984 ◽  
Vol 16 (1) ◽  
pp. 11-19 ◽  
Author(s):  
Rosmarie Honegger

AbstractThe contact sites of pycnidia and the terminal cells of trichogynes in Cladonia furcata were investigated using either freshly fixed material, or ascomatal primordia and pycnidia from which the gelatinous material either on the primordial surface, or in the pycnidial cavity, had been removed. The sickle-shaped conidia fused, tip first, with the cell wall of trichogynes. Circular holes of about the diameter of the conidia found in the cell walls of trichogynes arise from enzymatic degradation of the wall material by fusing conidia. As the conidia appear to stick on any gelatinous surface material of the thallus the adhesion process is presumed to be unspecific.


1988 ◽  
Vol 66 (5) ◽  
pp. 915-925 ◽  
Author(s):  
R. A. Brammall ◽  
V. J. Higgins

Root colonization of tomato cultivars susceptible or resistant to Fusarium crown and root rot disease, caused by the pathogen Fusarium oxysporum f.sp. radicis-lycopersici Jarvis & Shoemaker, was studied histologically. In seedlings of susceptible cultivars ('Ohio MR13', 'Bonny Best', and 'Vendor') held at 22 °C, direct penetration of epidermal cells occurred by 24 h after inoculation and colonization of suberized hypodermal cells and adjacent intercellular spaces by 72 h. The cortex was colonized between 72 and 96 h after inoculation and the stele was commonly colonized by 120 to 144 h. Colonization of the cortex and stele was associated with the breakdown of parenchymatous cell walls and middle lamellae near fungal hyphae. In cultivars resistant by a single dominant gene ('CR6', 'Larma', and 'B82-865') colonization was similar to that in susceptible cultivars until 72 h after inoculation. By this time, papillae were abundant within hypodermal cells. Successful colonization of hypodermal sites was associated with the incorporation of phenolic or lignin-like materials and suberin within cell walls of the underlying cortex. These cortical wall modifications were paralleled by the deposition of electron-opaque material into cortical cell walls and middle lamellae and the production of finely granular bands around the peripheries of colonized intercellular spaces. Phenolic-containing structural defensive barriers (i.e., papillae and modified cortical cell walls) appear to be important in limiting fungal colonization in cultivars possessing single dominant gene resistance to this disease.


1981 ◽  
Vol 59 (1) ◽  
pp. 1-7 ◽  
Author(s):  
Robert A. Blanchette ◽  
John B. Sutherland ◽  
Don L. Crawford

The greenish-brown margin of discolored wood in three living silver maple trees, Acer saccharinum L., was examined by scanning electron microscopy and microbiological culture techniques. Micrographs of xylem vessels revealed filamentous structures; some of them appeared to be actinomycetous hyphae. Actinomycetes identified as Streptomyces parvullus Waksman & Gregory, S. sparsogenes Owen, Dietz & Camiener, and a third Streptomyces strain were isolated repeatedly from discolored wood of each tree. These isolates grew in liquid media in the presence of 0.1% (w/v) concentrations of several phenols. Although other phenols included in the test were not substantially degraded, p-hydroxybenzoic acid was utilized as a carbon source by S. parvullus. All three actinomycetes inhibited growth of selected wood-inhabiting fungi when paired on malt agar. When inoculated on sterilized sapwood and discolored wood from silver maple, the actinomycetes colonized vessel walls and occlusions, but were not observed to decay cell walls.


1991 ◽  
Vol 69 (7) ◽  
pp. 1552-1556 ◽  
Author(s):  
M. Muntanola-Cvetković ◽  
Jelena Vukojević ◽  
M. Mihaljčević

The systemic nature of the disease of sunflower plants caused by Diaporthe helianthi, the leaf–petiole–stem route of the host invasion by the fungus, and the plant tissues that were successively affected were demonstrated through histological studies. After penetration into the host, the infection hyphae invade the intercellular spaces and terminal veinlets of the lamina and spread toward larger branches of the conducting system, the midrib, and the petiole. Xylem elements are invaded but are affected less by the fungus attack than the phloem and the parenchyma tissues, which disintegrate completely. Hyphae spread through the leaf axil to the tissues of the stem cortex, where pycnidia of the Phomopsis anamorph are initiated from internal masses of mycelium. Key words: systemic plant diseases, sunflower diseases, Diaporthe helianthi, Phomopsis helianthi.


IAWA Journal ◽  
2005 ◽  
Vol 26 (2) ◽  
pp. 161-174 ◽  
Author(s):  
Hisashi Abe ◽  
Ryo Funada

We examined the orientation of cellulose microfibrils (Mfs) in the cell walls of tracheids in some conifer species by field emission-scanning electron microscopy (FE-SEM) and developed a model on the basis of our observations. Mfs depositing on the primary walls in differentiating tracheids were not well-ordered. The predominant orientation of the Mfs changed from longitudinal to transverse, as the differentiation of tracheids proceeded. The first Mfs to be deposited in the outer layer of the secondary wall (S1 layer) were arranged as an S-helix. Then the orientation of Mfs changed gradually, with rotation in the clockwise direction as viewed from the lumen side of tracheids, from the outermost to the innermost S1 layer. Mfs in the middle layer of the secondary wall (S2 layer) were oriented in a steep Z-helix with a deviation of less than 15° within the layer. The orientation of Mfs in the inner layer of the secondary wall (S3 layer) changed, with rotation in a counterclockwise direction as viewed from the lumen side, from the outermost to the innermost S3 layer. The angle of orientation of Mfs that were deposited on the innermost S3 layer varied among tracheids from 40° in a Z-helix to 20° in an S-helix.


1988 ◽  
Vol 66 (6) ◽  
pp. 1117-1128 ◽  
Author(s):  
Katharine E. Duff ◽  
John P. Smol

Twenty-six chrysophycean stomatocyst morphotypes were described from the postglacial sediments of a small, rock basin lake near Baird Inlet, Ellesmere Island. Scanning electron and light microscopy were used to classify the stomatocysts, following the guidelines of the International Statospore Working Group. None of the stomatocysts could be related with certainty to the chrysophyte species that produced them, but sufficient morphological detail is present in most of the stomatocysts to allow for taxonomic differentiation. A stratigraphic analysis of the dominant stomatocyst morphotypes revealed that chrysophyte species composition changed most markedly during the lake's early development but then remained relatively constant. This study demonstrated that chrysophycean stomatocysts provide useful paleoecological information in High Arctic lakes, but further taxonomic and ecological research is required to fully exploit these microfossils.


2017 ◽  
pp. 66
Author(s):  
Aída Carrillo-Ocampo ◽  
E.M. Engleman

With methods of light microscopy, histochemical staining and scanning electron microscopy, it was found that the ovule in the seed of Tigridia pavonia (Iridaceae) is anatropous, bitegmic, and crassinucellate. During development, the exotegmen is crushed and the endotegmen persists with tannins in the lumens and in the walls, which also react positively for lignin. The exotesta contains tannins and its outer walls are convex, thickened, and cuticularized. The mesotesta has multiple layers, accumulates abundant lipids, and forms a bulge in the chalaza. The cell walls of the endotesta collapse and accumulate tannins. In the chalaza, a hypostasal cushion contains tannins in the lumens and in the walls, which also react positively for lignin. At the micropylar end of the seed there is an operculum which consists of: a) a slightly crushed exotegmen, b) an endotegmen with cuticular thickenings that are concentric with respect to the micropyle, c) hemispherical deposists of cutin on the anticlinal walls of the endotegmen, and c) a thin layer of endosperm that covers the radicle. During its cellular stage of development, the endosperm has conspicuous transfer walls at the chalazal end next to the nucella. The embryo is small and has a conical cotyledon.


2008 ◽  
Vol 9 (9) ◽  
pp. 2510-2516 ◽  
Author(s):  
John H. Grabber ◽  
Ronald D. Hatfield ◽  
Fachuang Lu ◽  
John Ralph

Sign in / Sign up

Export Citation Format

Share Document