FDTD simulation of optical phase contrast microscope imaging

Author(s):  
Stoyan Tanev ◽  
James Pond ◽  
Paul Paddon ◽  
Valery V. Tuchin
2008 ◽  
Author(s):  
Stoyan Tanev ◽  
James Pond ◽  
Paul Paddon ◽  
Valery V. Tuchin

1958 ◽  
Vol s3-99 (48) ◽  
pp. 475-484
Author(s):  
VISHWA NATH ◽  
BRIJ L. GUPTA ◽  
S. L. MANOCHA

A study of the oocytes of the earthworm, Pheretima posthuma, examined fresh under the phase-contrast and interference microscopes as well as by histochemical techniques, has revealed that there are two types of lipid bodies in the cytoplasm. The lipid bodies of the first type (L1) are smaller, appear as homogeneous, dark granules under the phase-contrast microscope, and have a protein-phospholipid core surrounded by a thick sheath of phospholipids only. The lipid bodies of the second category (L2), which arise as a result of growth and chemical change in L1 bodies, have a pure phospholipid core surrounded by a thick triglyceride sheath. They give a ringed appearance under the phase-contrast microscope. The study under the interference microscope shows that this ringed appearance is an optical artifact. The lipid spheres present in the follicular epithelium contain phospholipids only. The mitochondria are in the form of minute granules. They remain unchanged throughout oogenesis. Some vacuoles devoid of any lipids, proteins, or carbohydrates have been observed. They also remain unchanged. Pure triglyceride spheres, yolk globules, nucleolar extrusions, as well as cholesterols and cholesteryl esters are absent.


Zootaxa ◽  
2018 ◽  
Vol 4527 (3) ◽  
pp. 414
Author(s):  
ELIDA P. MARÍN ◽  
JOSÉ G. PALACIOS-VARGAS

Neelus fimbriatus is redescribed using specimens from Colombia. Drawings and phase contrast microscope photos of the species are used. New characters are used as tibiotarsal tuberculate setae and abdominal ventral acetabula. 


Development ◽  
1970 ◽  
Vol 24 (2) ◽  
pp. 249-255
Author(s):  
J. B. Gurdon ◽  
R. A. Laskey

Two methods of transplanting single nuclei from monolayers of cultured cells to unfertilized eggs of Xenopus laevis are described, illustrated, and tested. The detached-cell method is simpler and quicker to operate and is suitable for homogeneous populations of cells which are easily removed from the substrate on which they are growing. The other, attached-cell, method is technically more elaborate, but is applicable to cells whose properties can be individually determined under the phase-contrast microscope and to cells which are not readily dissociated from other cells or from their substrate.


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