Open all the planes and do Image > Stack > Images to Stack to collect them
into one window (called a "z-stack").
Then do Image > Stack > Z Project. Choose either Min or Max projection
depending on the type of images you took.
There are also plugins for "extended depth field" you can search for and
run on your z-stack.
-Esteban
On Jun 13, 2017 11:57 AM, "Denise Dagnino" <
[hidden email]> wrote:
Hi
I am new to ImageJ. I am trying to count phytoplankton in an
hematocytometer. The cells, no matter how much I wait, do not sediment.
Further I can clearly notice that as time passes the volume rather quickly
decreases under the slide and this wolud result in wrong counting.
What I did was to take pictures in several planes. I would like manipulate
each of them so as to only observethe cells in focus and then stack all the
different focus plains and then count.
Any suggestions on strings of commands I should execute?
Thanks for any help.
Denise
**********************************************************************
Dr. Denise Dagnino
Universidade Estadual do Norte Fluminense
Centro de Biociências e Biotecnologia
Laboratório de Biotecnologia
Av. Alberto Lamego 2000
BR - 28013-602 Campos dos Goytacazes - Brasil
+ 55 22 2739 7089 <+55%2022%202739-7089>
+ 55 22 2739 7031 <+55%2022%202739-7031>
*********************************************************
--
ImageJ mailing list:
http://imagej.nih.gov/ij/list.html--
ImageJ mailing list:
http://imagej.nih.gov/ij/list.html
Locked
