euglenozoa
Posted: Fri Sep 27, 2019 2:25 pm
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Quite a varied lot. Surprised me, was not expecting much.What other protozoans did you see in that sample?
In this case that was not a problem as there was some large detritus that kept the cover slip from moving down, the downside of course was that the image quality suffered as several of the smaller subjects were not pressed up against the glass - the equivalent of having a thicker cover slip than recommended, which with the 63x/1.4 is very noticeable.How did you manage the oil immersion? There seems to be quite a thick liquid layer under the coverglas and this usually causes issues for such high n.a. objectives (low working distance) and oil immersion (movement or "pumping" of the coverglas due to re-focusing)? .
Yes I did. In fact I always do. In for a penny in for a pound.Did you oil the top lens of the condenser?
I would not recommend all of them but some might do at a pinch if you run out of immersion oil.Wes wrote: ↑Sat Sep 28, 2019 9:37 pmLooking through the bertrand lens on the optovar unit I see an obvious difference upon oiling the condenser lens. Without oil I see a fairly limited field of illumination and following oiling the illuminated area increases dramatically. Now I wonder what difference there would be between using water, oil and other liquids with intermediate refractive index.
Nice list! I was thinking about glycerol, its very easy to clean as its water soluble and its refractive index is pretty close to the desired value.75RR wrote: ↑Sat Sep 28, 2019 10:15 pmI would not recommend all of them but some might do at a pinch if you run out of immersion oil.Wes wrote: ↑Sat Sep 28, 2019 9:37 pmLooking through the bertrand lens on the optovar unit I see an obvious difference upon oiling the condenser lens. Without oil I see a fairly limited field of illumination and following oiling the illuminated area increases dramatically. Now I wonder what difference there would be between using water, oil and other liquids with intermediate refractive index.