Expansion of the area vasculosa of the chick after removal of the ectoderm

Development ◽  
1970 ◽  
Vol 24 (1) ◽  
pp. 95-108
Author(s):  
J. M. Augustine
Keyword(s):  
Basement Membrane ◽  
Outer Surface ◽  
Chicken Embryo ◽  
Area Vasculosa ◽  
Inner Surface

The role of the ectoderm in the expansion of the mesoderm in the area vasculosa of the chicken embryo was studied. The basement membrane of the ectoderm was found to constitute a substratum for the expansion of both layers of mesoderm, since (a) the somatic mesoderm, particularly at its margin, adheres to the basement membrane, and (b) the somatic and splanchnic mesoderm adhere to each other throughout most of the area opaca. Following removal of the ectoderm from the outer surface of the basement membrane, movement of the underlying mesoderm along its inner surface stopped. Mean expansion of the mesoderm in these cases was zero. Following removal of both ectoderm and basement membrane, expansion of the underlying mesoderm was normal in amount. Experimental changes in the ectodermal substratum can thus stop movement of the associated mesoderm, but the role which the substratum normally plays in mesodermal expansion remains unclear.

A SEM and Light Microscope Study of the Epidermal Leaf Structures of the Carnivorous Plant, Sarracenia purpurea, L.

1971 ◽  
Vol 29 ◽  
pp. 358-359
Author(s):  
B. J. Panessa ◽  
J. F. Gennaro
Keyword(s):  
Methylene Blue ◽  
Toluidine Blue ◽  
Outer Surface ◽  
Microscope Study ◽  
Light Microscope ◽  
Carnivorous Plant ◽  
Sarracenia Purpurea ◽  
Inner Surface

Tissue from the hood and sarcophagus regions were fixed in 6% glutaraldehyde in 1 M.cacodylate buffer and washed in buffer. Tissue for SEM was partially dried, attached to aluminium targets with silver conducting paint, carbon-gold coated(100-500Å), and examined in a Kent Cambridge Stereoscan S4. Tissue for the light microscope was post fixed in 1% aqueous OsO4, dehydrated in acetone (4°C), embedded in Epon 812 and sectioned at ½u on a Sorvall MT 2 ultramicrotome. Cross and longitudinal sections were cut and stained with PAS, 0.5% toluidine blue and 1% azure II-methylene blue. Measurements were made from both SEM and Light micrographs.The tissue had two structurally distinct surfaces, an outer surface with small (225-500 µ) pubescent hairs (12/mm2), numerous stoma (77/mm2), and nectar glands(8/mm2); and an inner surface with large (784-1000 µ)stiff hairs(4/mm2), fewer stoma (46/mm2) and larger, more complex glands(16/mm2), presumably of a digestive nature.

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.

scholarly journals The potential role of microRNAs in regulating gonadal sex differentiation in the chicken embryo

2011 ◽  
Vol 20 (1) ◽  
pp. 201-213 ◽  
Author(s):  
Andrew D. Cutting ◽  
Stephanie C. Bannister ◽  
Tim J. Doran ◽  
Andrew H. Sinclair ◽  
Mark V. L. Tizard ◽  
...  
Keyword(s):  
Chicken Embryo ◽  
Potential Role ◽  
Sex Differentiation

Role of laminin in the attachment of PAM 212 (epithelial) cells to basement membrane collagen

Cell ◽  
1980 ◽  
Vol 22 (3) ◽  
pp. 719-726 ◽  
Author(s):  
Victor P. Terranova ◽  
David H. Rohrbach ◽  
George R. Martin
Keyword(s):  
Epithelial Cells ◽  
Basement Membrane ◽  
Basement Membrane Collagen ◽  
Membrane Collagen

scholarly journals The first data on the role of rhyncholites in the process of epibiota

2019 ◽  
pp. 5-9
Author(s):  
E. S. Gaponenko ◽  
M. A. Ulshin ◽  
V. N. Komarov
Keyword(s):  
Adult Worm ◽  
Dorsal Surface ◽  
Ventral Side ◽  
Ventral Surface ◽  
Clear Indication ◽  
Life Activity ◽  
Additional Food ◽  
Inner Surface ◽  
First Time

For the first time the role of rhyncholites in the process of epibiota has been figured out. Serpulidae inlay is detected in 39 rhyncholites of 979 specimens, representing 4% of the all studied material. This fact demonstrates that rhyncholites were used extremely rarely by encrusting species as a substrate. No other epibionts were found. Polychaetes were found in the genus Hadrocheilus (87%) and in the genus Akidocheilus. Size of the inlaid rhyncholites ranges from 7 to 23 mm. Serpulidae cover usually only the ventral side of rhyncholites, herewith, at 48,7% of the samples epibionts with different degrees of intensity are developed throughout the ventral surface, at 30,7% of the samples they are observed only on the ventral side of the hood and at 20,6% serpulidae are present only on the ventral surface of the arm. At four exemplars of the genus Hadrocheilus (10 % of the total amount) polychaetes are developed on the dorsal surface, but they are always and usually very wide developed on the ventral side of rhyncholites. No samples were found in which serpulidae were found only on the dorsal surface. Among the remains of polychaete worms, large and small tubes were identified and described. The presence of serpulidae on the handle of rhyncholites, that during the life of the cephalopod mollusk was located in a horny jaw, is a clear indication of the settlement’s epibionts on isolated skeletal structures of the already dead cephalopod. Cases when serpulidae are observed only on the ventral side of the hood in representatives of the genus Akidocheilus, suggest that planktonic trochophore – larvae of polychaetes can settle on the inner surface of the mandible of living ammonoids, where they turned into an adult worm. At the same time, polychaetes gained access not only to traditional prey, represented by various microscopic organisms, but also to additional food resources associated with the life activity of cephalopodas.

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