Our objective was to test the hypothesis that the pheromone blend and/or di
el periodicity of pheromonal communication differ in populations of the nun
moth, Lymantria monacha (Lepidoptera: Lymantriidae), from eastern Asia (no
rthern Honshu, Japan) and Central Europe (Bohemia, Czech Republic). Coupled
gas chromatographic-electroantennographic detection (GC-EAD) analyses of p
heromone gland extract of female L monacha from Japan confirmed the presenc
e of compounds previously identified in pheromone extracts of L. monacha fr
om Bohemia, as follows: (Z)-7-octadecene, 2-methyl-(Z)-7-octadecene (2me-Z7
-18Hy), cis-7,8-epoxy-octadecane (monachalure), and cis-7,8-epoxy-2-methylo
ctadecane (disparlure). Field experiments in Honshu suggested that (+)-mona
chalure is the major pheromone component of L. monacha. 2me-Z7-18Hy signifi
cantly enhanced attractiveness of (+)-monachalure. Addition of (+)-disparlu
re to (+)-monachalure plus 2me-Z7-18Hy in Honshu and Bohemia increased attr
activeness of lures by 1.2 and 20 times, respectively, indicating that (+)-
disparlure is of least and most significance in the respective L monacha po
pulations. Moreover, capture of male L. monacha in pheromone-baited traps b
etween 18:00 and 24:00 hr in Bohemia and 2:00 and 5:00 hr in Honshu reveale
d a markedly different diel periodicity of pheromonal communication. Pherom
onal communication late at night and use of (+)-monachalure, rather than ()-disparlure, as the major pheromone component by L. monacha in Honshu may
have resulted from interspecific competition with coseasonal L. fumida, whi
ch uses the early night for pheromonal communication and (+)-disparlure as
major pheromone component. Whether communication channel divergence of L. m
onacha in Honshu indeed constitutes a case of reproductive character displa
cement is difficult to prove. The evolution of such divergence in sympatric
populations of L. fumida and L. monacha would have to be demonstrated.