Surface Ultrastructure of Spores in Three Genera of Balanosporida, Particularly in Minchinia armoricana Van Banning, 1977. The Taxonomic Significance of Spore Wall Ornamentation in the Balanosporida

1981 ◽  
Vol 67 (6) ◽  
pp. 866 ◽  
Author(s):  
Frank O. Perkins ◽  
Paul van Banning

Phytotaxa ◽  
2016 ◽  
Vol 252 (3) ◽  
pp. 217
Author(s):  
TEODOR T. DENCHEV ◽  
HANG SUN ◽  
CVETOMIR M. DENCHEV ◽  
DAVID E. BOUFFORD

A new smut fungus, Sporisorium capillipedii-alpini (Ustilaginales), and a new species of grass, Capillipedium alpinum (Poaceae), on which it is growing, are described and illustrated. The collections were made in western Sichuan, China. Capillipedium alpinum differs from other species of Capillipedium by its diminutive size and short, slender inflorescence. Sporisorium capillipedii-alpini is compared with the species of Sporisorium with similar symptoms (destroying all spikelets of an inflorescence) that infect Capillipedium, Botriochloa, and Dichanthium. The new smut fungus differs from these species as follows: from Sporisorium taianum by having larger spores with minutely echinulate spore walls, from S. dichanthicola by having larger spores, from S. sahayae by having lower spore wall ornamentation and thinner spore walls, from S. andropogonis-annulati by having larger spores, and smaller sterile cells with thinner walls, and from S. mysorense by possessing minutely echinulate spore walls and differently colored spores and sterile cells. The types of S. andropogonis-annulati, S. mysorense, and S. sahayae were re-examined and detailed descriptions of these species are given. A key to the smut fungi of Sporisorium, that infect Capillipedium, Botriochloa, and Dichanthium and destroy all spikelets of the inflorescence of an infected plant, is also provided.



Author(s):  
A.S. Alqurashi ◽  
J. Kerrigan ◽  
K.G. Savchenko

A smut fungus that hinders wiregrass restoration efforts in longleaf pine-grassland ecosystems was collected from Aristida stricta and A. beyrichiana (Poaceae) in three states in the southeastern USA. Morphological and phylogenetic characteristics of this fungus were examined. These data show that the specimens from both plant species were infected by the same fungus and represent a new species of Langdonia. The new species differs morphologically from other species of Langdonia by teliospores being solitary and not compacted into spore balls. Spore wall ornamentation and teliospore size also differ from other Langdonia species. Phylogenetic analyses of DNA sequences of the ITS, LSU, and EF-1α supported separation of the species from A. stricta and A. beyrichiana from other Langdonia species. Based on these results, a new species, Langdonia walkerae, is proposed.



1969 ◽  
Vol 15 (12) ◽  
pp. 1472-1473 ◽  
Author(s):  
R. K. Fujii ◽  
W. M. Hess

Surface characteristics of conidia from monosporous cultures of Penicillium digitatum and Aspergillus nidulans var. echinulatus were studied by use of freeze-etch replicas. Surface configurations of coni8dia of both fungi were so variable that spore wall patterns do not appear to be consistent enough to have taxonomic significance at the strain or subspecies level.



1989 ◽  
Vol 67 (11) ◽  
pp. 3315-3365 ◽  
Author(s):  
J. A. Parmelee

Fifty-three taxa in 11 genera are described and illustrated from the Canadian Arctic. Included are a key to the genera and keys to the species within each genus. Prior records in many journals mostly lacked illustrations. Herein light microscope photographs are complemented by SEM photographs to show spore wall ornamentation, an essential character in species delimitation.



1995 ◽  
Vol 73 (11) ◽  
pp. 1761-1767 ◽  
Author(s):  
Li-Tzu Li ◽  
James W. Kimbrough

Pseudoplectania and Plectania currently belong to the Sarcosomataceae, tribe Sarcosomateae, a group with members lacking cyanophilic spore markings (absorbing a blue stain). The two genera are morphologically similar in having blackish discoid-shaped apothecia but differ in having globose and ellipsoid spores, respectively. Ultrastructural studies show that ascospores of Pseudoplectania nigrella (Pers. ex Fr.) Fuckel lack a secondary wall layer. On the contrary, Plectania nannfeldtii Korf has secondary spore wall ornamentation that is cyanophilic under a light microscope. The data suggest retention of Pseudoplectania nigrella in the Sarcosomateae; however, the position of certain species of Plectania needs to be reevaluated. Key words: Pezizales, Plectania, Pseudoplectania, Sarcosomataceae, spore ontogeny, ultrastructure.



Author(s):  
Mai M. Said ◽  
Ramesh K. Nayak ◽  
Randall E. McCoy

Burgos and Wislocki described changes in the mucosa of the guinea pig uterus, cervix and vagina during the estrous cycle investigated by transmission electron microscopy. More recently, Moghissi and Reame reported the effects of progestational agents on the human female reproductive tract. They found drooping and shortening of cilia in norgestrel and norethindrone- treated endometria. To the best of our knowledge, no studies concerning the effects of mestranol and norethindrone given concurrently on the three-dimensional surface features on the uterine mucosa of the guinea pig have been reported. The purpose of this study was to determine the effect of mestranol and norethindrone on surface ultrastructure of guinea pig uterus by SEM.Seventy eight animals were used in this study. They were allocated into two groups. Group 1 (20 animals) was injected intramuscularly 0.1 ml vegetable oil and served as controls.



Author(s):  
S. Mukherjee ◽  
T. Guha ◽  
B. Chakrabarti ◽  
P. Chakrabarti

The cervix is an important organ in reproduction. Its malfunction is frequently a factor for infertility. Ectocervix region does not appear to have received much attention although many studies have been reported on the endocervix. We report here our SEM observations on ectocervix in certain pathological conditions compared to normal ectocervix.Ectocervix specimens from human females with specific pathological disorders were processed for Scanning Electron Microscopy by conventional method and they were examined in a Philips SEM.The normal ectocervix is lined by flat layer of squamous epithelial cells with microridges (Fig. 1). These cells are known to be formed from columnar cells through metaplastic transformation. The cells of carcinoma-bearing ectocervix show a disorganised appearance (Fig. 2). In non-malignant tumour surface some cuboidal and few columnar cells were seen (Fig. 3). A cyst appears like an overgrowth on the surface of the squamous epithelium (Fig. 4). In ulcerated ectocervix a marked reduction of epithelial cells are observed (Fig. 5); the cells are devoid of microridges and, the large polygonal cells, as observed in normal tissues, have somehow acquired comparatively small hexagonal shape



Author(s):  
J. E. Laffoon ◽  
R. L. Anderson ◽  
J. C. Keller ◽  
C. D. Wu-Yuan

Titanium (Ti) dental implants have been used widely for many years. Long term implant failures are related, in part, to the development of peri-implantitis frequently associated with bacteria. Bacterial adherence and colonization have been considered a key factor in the pathogenesis of many biomaterial based infections. Without the initial attachment of oral bacteria to Ti-implant surfaces, subsequent polymicrobial accumulation and colonization leading to peri-implant disease cannot occur. The overall goal of this study is to examine the implant-oral bacterial interfaces and gain a greater understanding of their attachment characteristics and mechanisms. Since the detailed cell surface ultrastructure involved in attachment is only discernible at the electron microscopy level, the study is complicated by the technical problem of obtaining titanium implant and attached bacterial cells in the same ultra-thin sections. In this study, a technique was developed to facilitate the study of Ti implant-bacteria interface.Discs of polymerized Spurr’s resin (12 mm x 5 mm) were formed to a thickness of approximately 3 mm using an EM block holder (Fig. 1). Titanium was then deposited by vacuum deposition to a film thickness of 300Å (Fig. 2).







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