"Infusoria" was the old-fashioned aquarist's quaint expression
for a dense culture of protozoans, especially
rotifers and ciliates such as Paramecium but including flagellates and amoebas. An
infusion is a watery solution produced by
steeping or macerating vegetable matter;
the summertime "sun tea" you brew
out on the deck is an infusion. "Infusoria"
populations bloom in infusions of manure
or decaying vegetation. The most nutritionally
desirable of the planktonic protists are
probably rotifers, but the ciliates also
provide good nutrition. The most familiar
among the ciliates is Paramecium, the "slipper animalcule" you might
remember from High School Biology. Paramecia
multiply mostly by fission, with a little
sex on the side from time to time. This flexible
strategy helps them multiply very fast, so
your culture will be mature in a matter of
days. Paramecia and other non-photosynthesizing
single-celled planktonic creatures feed on
bacteria that are breaking down organic substances.
So to culture them, you need to supply some
decaying organic material, and to be patient
for about four days' time at temperatures
in the low 80s.
The "infusoria" culture you're
after is no more than a productive concentration
of the same "cloudy water" problem you avoid in the show aquarium.
When similar plankton appears unbidden as a white bloom, especially
in a new tank, we treat the phenomenon as
a problem instead of a food culture. Ciliates
and other microscopic plankton are always
present in a mature aquarium, but in comparatively
sparse numbers. They form an important link
in the food web.
Culturing. Requirements for a ciliate culture, or "infusoria,"
are simple: a starter culture plus organic
nutrients, exposed to strong daylight (but
not sunlight) and warmth (83oF is the ideal), at a stable and somewhat
alkaline pH above pH 7.0. The culture should
be cloudy but not milky-opaque, with a ripe
"pond" odor but not a foul bacterial
stink. Nevertheless, your family will really want you to keep a paramecia culture covered
with a sheet of glass. Culture water that
is too rich in organics, combined with not
enough aeration, will simply encourage bacterial
fermentation, which isn't what you want.
The starter can be filter-sponge squeezings
in water from a well-established planted
aquarium that hasn't been medicated recently.
Or water from a fishfree plant nursery. Even
water from a flower vase, as long as there
were no additives in the water, would be
more productive than raw, de-chlorinated
tapwater. As I've mentioned, my own soft
water needs a shallow layer of crushed coral
to keep the pH above 7.0.
Organic nutrients spark the bacterial decomposition
that forms the base of this rough-and-ready
ecosystem. So you'll need to add some vegetal
matter. Hay softened by boiling was traditional.
Rotting leaf mold, oil-free lawn clippings,
rabbit droppings, powdered cereal or instant
mashed potatoes, baby food or hardboiled
egg yolk crumbs, or stale fish food--— they
all work. Wilted lettuce leaves left in the
dry air till they're brittle, then crumbled,
would be my first choice. Banana skins and
sliced potatoes tend to encourage a lot of
fungus, in my experience. If I were already
running a DIY CO2 setup, I might add just enough filtered
yeast culture to faintly cloud the water.
Snails in the culture are good. (Aren't some
Ampullaria even called "Infusoria Snails?")
Their droppings encourage the protists, and
the snails act like canaries in a mine shaft:
when my Melania snails crawl above water
level, it's high time to re-culture!
You may think you can skip this first stage
by feeding the fry with a commercially-bottled
liquid fry nutriment. These liquid fry feeds
get very mixed reviews from experienced fishkeepers;
one group states that whatever good such
products are doing is possibly in providing
a source of decay bacteria, which in turn
feed the culture of protozoans that you're
really after. In fact, a few drops of skim
milk or liquid fry food are often recommended
in culturing paramecia.
There are rigorous laboratory directions
for culturing paramecia under sterile lab
conditions in "The Zebrafish Book: a
guide for the laboratory use of zebrafish
Danio" part of information for biologists
deciphering the zebrafish genome at the Zebrafish Information Network. Don't be too proud to look through "Zebrafish
for K-12" also. In the lab culturing
directions, you use distilled water, a brewer's
yeast tablet, boiled wheatseeds (the "wheatberries"
of your local healthfood store) and a seeding
from a good clean young paramecium culture,
all stored in strong light (not sunlight)
and ready in 4 days at 28.5oC. That would be 83oF. You may not go about culturing so meticulously,
but isn't it good to know the ideal temperature
of a paramecium culture?
Charlie Grimes' simplest possible recipe
for culturing a mix of Euglena and paramecium
(the commonest kind of free-swimming ciliate)
in Aquarium Fish, April 1997, required no more than a gallon
jar of clean aquarium water and a dried pea!
It has never been quite that simple for me.
Mike Edwardes suggests putting a slice of boiled potato
in some rich old tank water, incubated in
a brightly-lit window till it's cloudy with
bacteria. He suggests continuous light aeration,
as low oxygen levels inhibit aerobic bacteria.
As the water clears, the protozoans are at
their most numerous--— in 3 or 4 days.
Francisco Borrero had this "boiled greens"
technique from his mother, a commercial breeder
of danios and other egglayers:
"This is the best way I've found of
producing good infusoria cultures for feeding
small fry: I take several spinach leaves,
any variety, and rinse them very well. Spinach,
collard greens and probably others work just
as well. Best but not strictly necessary
is to use organic, or certified as with no
pesticide. If it is not fresh it does not
matter and may be even better. Put in a pot
(I prefer a glass pot) and bring to just
past boil. Turn off inmediately after boiling
temp, or even just before. - Let this green
water cool to room temp. I do this by placing
it outside on the porch, uncovered. This
may help innoculation. —Use as a food for
infusoria cultures. If you let it sit in
a wide mouth jar for a couple of days, it
will "develop" infusoria. (quotations
intended to avoid suggesting spontaneous
generation, which of course does not happen).
What I really do is to innoculate a fresh
batch of cooled green water with a small
amount of infusoria innoculum taken by pipet
from a rich infusoria culture produced in
the standard manner. Wait 1-3 days depending
on temperature. - The result is much cleaner,
denser and longer-living infusoria cultures
than with standard methods. This method results
in the virtual absence of the nasty bacterial
decay film which is bad for fish fry, and
bad for the infusoria culture. After producing
the first culture by the lettuce green water
method, I use this as an innoculum for suceeding
batches. I start a new jar every 3rd day
or so, allowing having constant supply of
clean cultures. Start with clean jars. Soap
residues in jars will result in slow or no
culture happening."
Adrian Tappin"s "Feeding Rainbowfishes"
section at "Home of the Rainbowfish" has some further culturing techniques.
Aquaculture Supply
(with a link to their "aquasales.com")
will sell you greenwater and plankton culture
kits, with their famous and universally-recommended
Plankton Culture Manual.
Feeding. The trick with feeding from a culture or
innoculating a new one is getting a rich
dropperful of paramecia without too many
bacteria. Often there's a scummy lipid layer
at the surface you'd also like to avoid.
Ideally, you'd like to keep a steady supply
of ciliates and rotifers available to your
larval fishes, without actually culturing
"infusoria" right in the fry tank.
Try this: as the culture matures, the bacteria
will use up most of the oxygen as they work
on decomposing the organic substances. First,
turn off any aeration you may be using. The
resulting lowered oxygen levels through most
of the culture will encourage the protists
to gather after some hours in a shimmering
milky layer in the only place where the stagnating
culture medium contains some oxygen diffusing
in from the atmosphere--— just under the
surface. From there, you can draw them up
in a syringe or a large eye dropper.
Alternatively, you can extract some paramecium
culture in your "aquarium only"
turkey baster and fill a tall narrow bud
vase. After ten hours or so, you'll have
a clean concentrated layer of ciliates at
the top of the vase. With an eye dropper,
you can remove them, either for feeding fry...
...or for seeding a more selective second
culture of infusoria. The first culture you
develop, using rich old unmedicated aquarium
water, may prove to be less than select.
But draw out some culture from the paramecium
layer and re-culture that. Since paramecia
multiply so quickly, they will outpace other
plankton in the re-cultured medium. You'd
better keep a couple of infusoria cultures
going while you need them, because nothing
crashes more unexpectedly than populations
of protists.
This page last updated: 09/09/05 01:44:04 AM
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