'Apilife VAR' has been developed to combat Varroa jacobsoni in bee col
onies. It consists of a Vermiculite plate which is loaded with about 2
0 g of a mixture of thymol (76%), eucalyptol (16.4%), menthol (3.8%) a
nd camphor (3.8%). The purpose of these tests was to examine the effic
iency of the product in the following conditions: a) duration of the t
reatment: 4 or 8 weeks; b) dosage in Swiss hives: twice 1 plate, twice
1/2 plate or once 1 plate; c) formulation: with or without camphor; d
) disposition of the plates in Swiss hives, directly on the brood comb
s or on a fine-meshed grid positioned on the combs; e) disposition of
the plates in Dadant and Ritter hives: directly on the combs (above) o
r under the bottom grid (below). Problems related with bee toxicity, c
oncentration of the components of the product in the air of the hive a
nd residues in the bee food and honey have also been examined. In the
Swiss hive the average efficiency of 'Apilife VAR' was 97.7% after 8 w
eeks of treatment and 93.7% after 4 weeks of treatment. The difference
was not significant. Twice 1 plate was the best dosage in the Swiss h
ive. The difference of formulation (with or without camphor) did not i
nfluence the results of the treatment (table I). The fine-meshed grid
between the brood comb and the plate did not change substantially the
efficiency of the product as long as the bees did not cover the grid w
ith propolis. In the Dadant and Ritter hives the treatment from below
was not efficient enough (table II). The treatment from above had an e
fficiency of 97.1% in the Ritter hives and of 89% in the Dadant hives.
A method for the estimation of the number of varroas remaining in the
colony after application of 'Apilife VAR' is presented. It is based o
n the correlation (r = 0.867) between the number of dead varroas found
on the hive bottom during the first 2 weeks after the 'Apilife VAR' t
reatment and the number of dead varroas after the subsequent Perizin t
reatment (fig 1). If less than 1 varroa falls per day, the remaining v
arroa population will be lower than 100. If this condition is filled n
o further measures must be taken. 'Apilife VAR' did not influence the
mortality of the bees and the development of the colonies. The thymol
concentrations of the air of 4 bee colonies varied from 1.1 to 21.3 mu
/l. Whereas the values were equilibrated in the Swiss hives, they fluc
tuated considerably in the Dadant hives (fig 2). The eucalyptol, menth
ol and camphor concentrations were much lower. They varied between les
s-than-or-equal-to 0.02 and 2.4 mug/l of air. These concentrations hav
e probably no varroacidal effect. Only thymol residues were detected i
n the bee food and honey (table III). After 8 weeks of treatment the m
ean residue values were 2.6 mg/kg (SD +/- 2.0, n = 30) in the Swiss hi
ves and 2.0 mg/kg (SD +/- 0.98, n = 12) in the Dadant and Ritter hives
. The maximum value was 9.2 mg/kg. 8 months later the respective value
s in the spring honey harvest were 0.1 mg/kg (SD +/- 0.09, n = 30) and
0.03 mg/kg (SD +/- 0.01, n = 12), with a maximum value of 0.33 mg/kg.
The residues found in honey are innocuous to human health. Thymol is
generally recognized as safe ('GRAS' status), ie concentrations up to
50 mg/kg are considered unobjectionable. Before making a general asses
sment of 'Apilife VAR' it will be necessary to carry out further resid
ue measurements and to fix the perception threshold for thymol in diff
erent types of honey.