Thanks very much Mike and Jacek; I very much appreciate your kind comments.
Mike, in regards to your inquiry, there are many variables as I'm sure you in particular are quite aware. They would include the concentration of the solution, the rapidity of drying (as would be affected by heat or the addition of volatile agents), and the thickness of the solution. My approach on this crystal was a dilute aqueous solution spread onto a just-cleaned slide and allowed to dry overnight. Try both thick areas, as an individual droplet, and thinned areas with the solution spread over a larger area. My best result was with the thinned areas.
The scope is a regular Labophot with the addition of a small (about 25mm) polarizer at the base of the trinocular head. A second larger polarizer (found in a used camera store bin) is sitting atop the scopes light supply, just below the Nikon Phase Contrast-2 condenser (found on Ebay). The lower polarizer is rotated to extinction and is used without any partial wave modifier. The lens used is a Plan achro 20X Ph2 Nikon. I do my (underexposed) exposures in raw with a Nikon 810. After downloading, the exposure is adjusted and the background is reduced to an absolute black as needed. The stack is made from converted tiff files The final image is cleaned up in Photoshop.
Please note, I claim no expertise here, and just limited experience, but hey, you asked. I'd be delighted to hear the comments of any others who have been down this road.
Best,
Leonard
