EVALUATION OF 2 METHODS FOR RELEASE OF ENTOMOPHTHORA-MUSCAE (ENTOMOPHTHORALES, ENTOMOPHTHORACEAE) TO INFECT HOUSE-FLIES (DIPTERA, MUSCIDAE)ON DAIRY FARMS
Cj. Geden et al., EVALUATION OF 2 METHODS FOR RELEASE OF ENTOMOPHTHORA-MUSCAE (ENTOMOPHTHORALES, ENTOMOPHTHORACEAE) TO INFECT HOUSE-FLIES (DIPTERA, MUSCIDAE)ON DAIRY FARMS, Environmental entomology, 22(5), 1993, pp. 1201-1208
Two methods for initiating epizootics of Entomophthora muscae (Cohn) F
resenius in house fly, Musca domestica L., populations were evaluated
on New York dairy farms. First, 500 fresh, laboratory-infected fly cad
avers were placed weekly for 10 wk inside barns in areas of high fly a
ctivity. Second, 2,500 living, infected flies were released on each of
two occasions spaced 3 wk apart. Releases were started in mid-june. T
hree farms were used for each treatment plus three control farms. The
E. muscae used for the releases had been isolated from house flies col
lected from dairies the year before and had been maintained by continu
ous fly-to-fly passage. Prevalence rates on both types of E. muscae re
lease farms were twice as high (23-28%) as on control farms (12%) in t
he weeks after the start of the releases. Releases were more effective
OD farms with high fly populations than on farms with low fly populat
ions. Examination of conidia indicated that the released strain (8-18
nuclei per conidium) became established as a result of the releases. E
pizootics occurred on all farms, including controls, in September thro
ugh November. Infections in the spring were exclusively with a strain
of E. muscae with 2-8 nuclei per conidium; by fall, most infections (8
6-93%) were with a strain with 8-18 nuclei per conidium, even on contr
ol farms. Nuclear densities in the laboratory culture remained constan
t at 8-18 nuclei per conidium during this shift in wild infections. Ne
ither of the E. muscae treatments significantly reduced fly population
s.