Cryogenic Scanning Electron Microscopy of Early Stages of Film Formation in Drying Latex Coatings

Author(s):  
Erwin Sutanto ◽  
Yue Ma ◽  
H. T. Davis ◽  
L.E. Scriven
1996 ◽  
Vol 22 (2) ◽  
pp. 155-159 ◽  
Author(s):  
Manoj M. Haridas ◽  
Ashok Menon ◽  
Nitin Goyal ◽  
Sanjay Chandran ◽  
Jayesh R. Bellare

2019 ◽  
Vol 13 (4) ◽  
pp. 587-598 ◽  
Author(s):  
Maya Schnabel‐Lubovsky ◽  
Olga Kossover ◽  
Sonia Melino ◽  
Francesca Nanni ◽  
Yeshayahu Talmon ◽  
...  

Botany ◽  
2008 ◽  
Vol 86 (1) ◽  
pp. 45-52 ◽  
Author(s):  
Denis Barabé ◽  
Christian Lacroix

The early stages of development of the inflorescence of Anthurium jenmanii Engl. were examined using scanning electron microscopy. The inflorescence of A. jenmanii consists of more than 100 flowers arranged in recognizable spirals. Each flower has four broad tepals enclosing four stamens that are not visible prior to anthesis. The gynoecium consists of two carpels. The floral primordia are first initiated on the lower portion of the inflorescence, they then increase in size and appear as transversely extended bulges. The two lateral tepals are the first organs to be initiated, followed shortly thereafter by the two median tepals. The two lateral stamens are initiated first, directly opposite the lateral tepals, and are followed by two median stamens initiated directly opposite the median tepals. A two-lobed stigma is clearly visible during the early stages of development of the gynoecium. On some of the young inflorescences, all floral parts were covered by extracellular calcium oxalate crystals. The release of these prismatic crystals occurs before the stamens and petals have reached maturity. The mode of floral development observed in Anthurium has similarities with that reported for Gymnostachys . However, contrary to Gymnostachys, the development of the flower of A. jenmanii is not unidirectional.


2015 ◽  
Vol 1129 ◽  
pp. 331-338 ◽  
Author(s):  
Guo Rong Zhao ◽  
Pei Ming Wang ◽  
Guo Fang Zhang

Effect of latex film distributions on flexibility of redispersible polymer powders modified cement mortar were evaluated by scanning electron microscopy (SEM). Latex film distributions such as forming interpenetrated networks embedded in cement pastes, covering cement hydrates locally, bonding cement hydrates together, bridging aggregates were all beneficial for the improvement of flexibility of cement mortar. Latex film distributions such as remaining single particles in cement mortar, completing film formation unsuccessfully, film formation on surfaces of aggregates, bonding cement minerals to surfaces of aggregates may contribute little to the improvement of flexibility of cement mortar.


HortScience ◽  
2008 ◽  
Vol 43 (2) ◽  
pp. 361-365 ◽  
Author(s):  
Gilles Galopin ◽  
Sandrine Codarin ◽  
Jean-Daniel Viemont ◽  
Philippe Morel

Architectural development of inflorescence in Hydrangea macrophylla cv. Hermann Dienemann was observed using scanning electron microscopy. The study of inflorescence morphogenesis shows that the architecture is of the dichasial type. The first two orders of branching are initiated from a dichasial branching without floral differentiation. The following orders present floral differentiation. They determine the formation of small units through the development of composite dichasium into biparous and uniparous cymes. This research makes it possible to establish a schematic representation of the first phases of inflorescence development and to define early stages of inflorescence morphogenesis.


IAWA Journal ◽  
1993 ◽  
Vol 14 (3) ◽  
pp. 219-226 ◽  
Author(s):  
W. Wayne Wilcox

As part of a larger study of the microscopical characteristics useful in diagnosing early stages of decay, an opportunity was created to compare the ability of light microscopy (LM) and scanning electron microscopy (SEM) to image these features. Although most features could be imaged by both technologies, imaging was much easier in the SEM because it was being used at the low end of its resolution and magnification capability while the LM was near the high end of its limitations. One important feature which could not be imaged in SEM was the earliest attack on the cell walls, a feature which was visible under polarised light in the LM.


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