BAITING TRAPS FOR MICROBES
CILIATES AND FLAGELLATES
Teacher’s Resource Page
Objectives
Students will be able to
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Make baiting traps for capturing ciliates and flagellates;
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Enrich for ciliates and flagellates utilizing two kinds of food sources;
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Observe ciliates and flagellates in various aquatic habitats.
Skills
Observing, analyzing, comparing, problem solving
Materials
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Empty film canisters with lids
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Twine or rope
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Sharp razor blade
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Fingernail polish or crazy glue
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Nylon material
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Water-based tuna fish
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Cheese
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Small rocks or stones
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Microscope
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Small petri dishes
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Labeling pencil or pen
Grades
7 - 12
Subjects
Life Science, Biology, Integrated Science, Environmental
Science, Ecology, Microbiology
Time Needed
Approximately 2 class periods
Background
Protists are microbes found almost everywhere there is water.
A particularly rich environment is the still-water surface at the edges
of lakes and ponds.
Nearly all protists are aerobic in their metabolism, using mitochondria
for cellular respiration. Most protists are unicellular and have flagella
or cilia at some time in their life cycles, thus the name flagellates and
ciliates.
Protozoans refer to protists that live primarily by ingesting food.
These heterotrophs actively seek and consume bacteria, other protists,
dead organic matter, and manufactured food
Vocabulary
| aerobic |
heterotrophs |
protists |
| cellular respiration |
metabolism |
protozoans |
| cilia |
mitochondria |
unicellular |
| flagella |
|
|
Advance Preparation
Obtain canisters from film shop. Nytex, knee-highs, or pantyhose
work for nylon material. Be sure not to use the sheer brands due to adherence
problems. If you plan to perform this lab in your classroom with pond water,
you will need to get that ahead of time.
General Procedure
Tips for preparing canisters
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Using a sharp razor, cut a square window on the side of the film canister
2 cm from the bottom. Window should be cut towards the top of the canister.
Window should be no larger than 1 cum x 1 cm. Cut a piece of nylon material
so that it fits over the opening.
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Adhere nylon material by coating its sides with glue or polish. Make certain
to coat area around canister opening so that water will not fill nylon
around canister. Allow coats to dry and apply again.
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Soak canisters in water overnight.
Tips for preparing water samples
Canisters may be placed in
a
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still-water pond or lake
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tap water
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pond water brought into classroom
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artificial pond water (made from soil and water)
Tips for preparing baiting traps
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Press food in the bottom side of the canister.
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Place a small stone inside to weigh it down.
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Twine or rope should be tied to canisters placed in pond so that it does
not float away.
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Submerge open canisters in water and do not cap until filled to avoid bubbles.
Viewing samples
View in a small petri dish
under dissecting or compound microscope.
Specific Inquiry
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Discuss background on protozoans, ciliates, and flagellates.
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Have students make a food chain/web using decomposing food, bacteria, and
protozoans.
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Facilitate a discussion on how to trap ciliates and flagellates from water
based on what has been discussed and the food chain/web made.
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Explain how to make a baiting trap.
Suggested Questions for Analysis
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Did all the protozoa have flagella?
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Did each of the aquatic environments tested have the same protozoans?
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What types of behaviors did you see in flagellates?
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How do flagella help protozoa?
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Do cilia beat together or do they have their own rhythm?
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Do cilia beat in one direction, or can they change direction?
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Are all the cilia on one organism the same length or different lengths?
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Can you think of other types of cells besides flagellates that have a flagellum?
Extensions
Design an experiment to
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Find out if all species of flagellates live at all water levels or if different
species live at different levels.
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Determine if there is a correlation between depth of water and number of
protists captured.
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Observe patterns in water flow. (Hint: Stain with India ink to observe
water flow.)
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Observe and count bacteria in media. Take about 10 microliters of enriched
culture and place on nutrient agar plate. Spread with bacteria spreader
and observe colonies after a few days. You can count the number of colonies
you had in 10 microliters and determine the amount you have in 100 microliters.
This will give you an estimate.
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