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This is pollen from a tree in the flowerboxes outside Low Housing on campus here.

Using the Zeiss dissection microscope, we could take macro images (two color images at left and more here.).

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Using the Leica AOBS microscope, we could scan at high resolution.

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The pollen may be imaged by its own fluorescent emission.
When this pollen is excited with 405 nm light, this is the resulting spectrum:
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However, when exciting at 365 nm +/- 20 nm, we could see by eye that each grain had a distinct red line running through it.
This was not detected by the confocal with excitation by a single line at 40 nm longer.

Here is a series of thin optical sections taken through another grain.
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Click here for a 2.46MB movie of the montage above.
Although the corners of the grain cracked (probably due to rough handling), it shows the basic 3D structure.

 

 

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All material on this page © 2004 all right reserved by Michael Cammer and the Albert Einstein College of Medicine of Yeshiva University