SUBJECT: Elodea diffusion lab
DATE: 4/97
 
I was interested in the comments by SDSCHNELL (no sig) about using Elodea
for a diffusion lab. I'm wondering if it could be made a bit more
investigative in which students would determine the isotonic concentration.
I'm thinking they could be given a strong salt solution to dilute into a
series of tubes. Place an elodea leaf in each tube and after a time, look
at them under the scope.
 
Any thoughts about this?
 
My colleague says he has had problems with Elodea not shrinking like it
should, and neither of us could figure why that should be so.
 
Lane
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Lane Lester / llester@athens.net / Athens, Georgia USA
 
 
Time seems to be a factor. If you are wicking the salt under the
coverslip, watch the side closest to the addition. It can take what seems
to be a few minutes. I've never tried to time it. I'm sure there is a
dilution factor involved in this method as well. The highest concentration
will be near the source initially. --cmw
 
Charlene M. Waggoner, Ph.D. "Great art is eternal;
Department of Biological Sciences great science tends to be
Bowling Green, State University replaced by greater science."
Bowling Green, OH 43403
-- John A. Moore
cwaggon@bgnet.bgsu.edu
 
 
We do this in one of our intro courses and it works best with tips of young
leaves. We usually get plasmolysis in the range of 1-1.5% NaCl. Finer
concentrations can pinpoint it better.
 
Greg Anderson
Department of Biology "Dance you buggers, dance!
44 Campus Ave Or you'll never get to Heaven!"
Bates College
Lewiston, ME 04240 God, speaking to the Methodists,
from the song "The Last Dance"
by Peter Coe
ganderso@abacus.bates.edu
(207)786-6110
 
 
 
Most lab manuals insgtruct us to use a 1% NaCl solution. I use a 25%
solution and it does work.
 
Someone wrote about obtaining sheep blood since we can no longer use human
blood in public secondary schools.
 
I will look into this.
 
Stuart D. Schnell
Science Department
John C. Fremont High School
7676 South San Pedro Street
Los Angeles, CA 90003
 
 
>I'm wondering if it could be made a bit more
>investigative in which students would determine the isotonic concentration.
 
You can do this by looking for incipient plasmolysis (ie., inferred by a series of
dilutions whose % plasmolyses are graphed to determine 50% point). Have
students generate a series of concentrations from a 1M STK (0.1M, 0.2M, 0.3M, etc.) and
determine % plasmolysis for each concentration, then graph as indicated above.
 
A nice extension to this idea is to try salts of different valences (e.g, divalent = NaCl, KNO3;
trivalent = MgCl2) and even molecular compounds with different MW values
(e.g., glucose, glycerol). Students can compare incipient plasmolysis points and look for
relationships (e.g., concentration of trivalent < concentration of divalent @ incipient
plasmolysis, also lower MW has higher concentration @ incip. plasmolysis than higher MW
compd., all other things being equal).
 
Todd
Todd Bennethum, Science Teacher
Arapahoe High School
2201 E. Dry Creek Road
Littleton, CO 80122
 
e-mail: tbenneth@model.cudenver.edu
WWW: http://bilbo.bio.purdue.edu/~tbenneth
 
 
If anyone is looking for a good source for sheep blood, try Colorado Serum
Company (1-303-295-7527). They are reliable. I purchase the Alsiever's (sp?)
prep. It costs about $30-40 for a vial but this is more than enough for your
classes. The cells work wonderfully in a simple experiment using pure water,
3%NaCl and 0.9% NaCl. Just keep the blood refridgerated the week you want to
use it.
Sandy Buckles
Lab Instructor
John Carroll University
Cleveland, Ohio
(216)397-4486
sbuckles@jcvaxa.jcu.edu
 

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