Apiculture Factsheet #222
Varroa Mite Detection Methods
Effective mite control is dependent on frequent and
reliable detection. Varroa mites spread rapidly between hives
and bee yards due to drifting, robbing and hive movement. Mite
levels rise rapidly in late summer and early fall. In
heavily infested areas, individual colony infestations can grow from being
undetectable to life-threatening levels within a few months.
It is important to monitor mite levels by sampling all or
most colonies on a regular basis. Larger beekeepers should sample at
least 10% of the colonies in each yard in the spring and the fall.
Unusually large or small colonies and those at the end of
rows should be tested.
How Often To Monitor
Early detection offers the best opportunity
for effective Varroa control. Frequency of colony testing is as
follows:
- twice per year (spring and fall) - when mites are not thought to be
around;
- every two months (excluding winter) - when mites are known to
be around.
There are different detection methods available, some more
sensitive than others. Some methods require a mathematical
conversion to estimate the actual number of mites in a colony. A
colony's mite load will indicate the treatment necessary.
The following are a number of detection methods to choose from:
Sampling Brood
Up to 85% of the mites in a colony are in capped brood cells and
not visually detectable. Varroa mites are more attracted to drone brood
than worker brood, so look there first. Sample about 100 cells.
Locate a patch of drone cells in the purple eye pupal stage. Slide the
prongs of a de-capping fork along the comb face and into the
protruding drone cappings. Pry upward and remove the pupae.
Carefully examine the bodies and the interior of the cells for
mites.

Detection Boards
Boards are available commercially or can be prepared by
beekeepers. The commercial boards are covered with a sticky film
and require a screen (8-gauge) to prevent bee entanglement.
For home-made preparations, white sheets of paper, cardboard or
corrugated plastic (eg. Tenplast) can be cut to cover most of the
hive bottom surface (40 x 30cm / 16 x 12in). One side of the board surface should be covered
with a 1:1 mixture of cooking oil and petroleum jelly, or the
surface can be sprayed with a thin coating of PAM vegetable oil. A
cover screen is not required. Boards must be cleaned thoroughly before
reusing them to prevent mite transfer.
Install sticky board for 24 hours only. When
the board is left longer, there will be too much debris, making it difficult to count mites.
Apistan Strips (10% fluvalinate)
Apistan is applied in plastic strips and is a contact miticide.
It does not have an effect on mites developing in capped (bee) brood cells.
The use of Apistan strips in combination with a sticky board for
24 hours has proven to be a very effective method of determining infestation levels. For detection purposes, use recommendations below under
"CheckMite+".
CheckMite+ (Coumaphos)
Coumaphos is applied in plastic strips under the trade name
CheckMite+. Coumaphos does not kill mites
in sealed brood cells. When there is no brood in the colony, the
mite count on a sticky board will accurately reflect the colony's
infestation level. When brood is present, as much as 85% of the mite
population is
hidden under the capped brood cells.
For detection purposes, use one CheckMite+ or Apistan strip per
nucleus or two strips for a standard two-supered hive, where the
strips are placed between frames in the central brood area. Daytime
temperatures should be 10 degrees C or higher. Strips and sticky
board should be removed after 24 hours. For treatment
purposes, follow label instructions.
Mite Level Determination: Multiply the number of mites on a
board by 6.
Note: CheckMite+ or Apistan trips only used for detection purposes
can be re-used 10 times for 24-hour tests before disposing of them. Please
make sure that the strips are not exposed to sunlight. When not in use, store in a marked container in a
cool, dry and dark place.
Note: The development of mite resistance to
Apistan and CheckMite+ in parts of the province has made it
important to determine the efficacy of these products. For efficacy
testing, refer to Factsheet #223.
Formic Acid
Formic acid is used to control both Varroa and tracheal mites.
Several application methods have been developed. It is important to
recognize the factors that influence the efficacy of formic acid, including colony size, weather, condition and
behavior of the colony, etc. Notwithstanding its variability, formic
acid has been recommended for use as a component of overall mite
control strategy.
For detection purposes, apply 40 ml (1.5 oz) of 65%
concentration formic acid liquid onto several layers of paper towels placed on the top bars of the upper brood chamber. Use enough paper towels to prevent acid from dripping. Install a
sticky board and check after 24 hours.
Note: Do not apply Coumaphos, Apistan, formic acid or other
chemicals to a hive when honey supers are in
place. Use the Alcohol Wash, Ether Roll or Icing Sugar Roll method instead.
Mite Level Determination: Multiply the number of mites on a board
by 6.
Alcohol Wash Method
This method is simple, quick
and quite accurate when applied to a larger number of colonies in
the apiary. It doesn't require a second visit after 24 hours. The test is carried out as follows:
- Use a wide-mouth glass jar and scoop about 300 bees (~1 cup)
from the brood area. Make sure that the queen is NOT included!
- Add 50 ml (~ 2 oz) of windshield wiper fluid (or diluted
methyl hydrate, or rubbing alcohol) to the jar and shake
for several minutes.
- Remove lid and pour contents into a container covered with light metal
wire-mesh screen (8 mesh/in) or a coarse sieve. Repeat.
- Pour alcohol solution into a second container covered with
cheesecloth or fine sieve. Count number of mites.
Mite Level Determination:
No Brood: Multiply by 100 to estimate the total Varroa mite
population.
Plenty of Brood: Multiply by 600.
Ether Roll
This test is simple but less accurate than the Alcohol Wash
method because it is more difficult to obtain an accurate count of
the number of mites in the sample.
- Select a brood frame with plenty of adult bees, and preferably
with drone brood. Make sure the queen is NOT on the frame!
- Gently scrape 150-300 young bees from the frame using a wide-mouth jar.
- Apply a two second burst of ether (automotive starter fluid)
into the jar, replace the top and shake vigorously for 30
seconds.
- Gradually rotate the jar horizontally and look for any
mites sticking to the sides. Normally, the ether causes the bees
to regurgitate, making the sides sticky. If not, add a bit of
syrup or water.
Mite Level Determination:
No Brood: Multiply by 100 to estimate the total Varroa mite
population.
Plenty of Brood: Multiply by 600.
Icing Sugar Method
Instead of Ether Roll where all the bees are killed, icing sugar
can be used.
Procedure is as follows:
- Collect a lightly packed cup of bees (about 300 bees) from a
frame of uncapped brood.
- Quickly place bees into a wide-mouth jar fitted with a
1/8th wire mesh screen lid.
- Place two heaping tablespoons of sugar powder through the
screen.
- Shake jar thoroughly, tip it and shake five times like a salt
shaker.
- Dump the sugar containing the mites on a white flat surface.
- Repeat the above two steps until virtually no more sugar shakes out.
- Count the mites.
Mite Level Determination: When 5 mites or more are counted,
treat the colonies.
When to Treat?
After determining an estimate of the total number of mites in a
colony, it must be decided if and when to treat. In the spring,
before honey supers are in place, or in the fall, when honey supers
have been removed, treat when 15 mites or more are counted.
When honey supers are in place, use the following guidelines:
| # Mites/Col. |
Recommendation |
| less than 100 |
- not an immediate problem
- treat in September and October, after honey removal
- continue to monitor bimonthly
|
| 100 - 999 |
- mite infestation will have an economic impact
- treat as soon as possible after removing honey; start in
August, even if some crop potential is lost (winter bee
population must be protected)
- continue to monitor bimonthly
|
| 1000 mites + |
- colony collapse imminent
- remove supers and treat immediately
- treat again in October
|
For more information on Varroa Control Methods, refer to Factsheet #221.
03/12