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2. Rwiew of literature
2. 1. Systematics of Musca domestica:
The qenus Musca Linnaeu~, 17581 comes under the family Muacidae, suborder Cyclorrapha of the order Diptera. The family Muscidae
consists of 26 mcies, of which majoritv of them are "wild" and have
little public health immrtance. H m v e r , Msca domestica and
M. sorbena are considered to he of mblic health Imrtance beca~lae - - of their association with man and his environment and their possible
role in the transmission of infectious aqents. 2. domesticar a
tmical synanthroaic f l v ( s ~ n = to-qether: anthmmic = man) is
comnonlv called as house flv and which is vidtrly distributed in
t m r a t e zones all over the world, even extendinq t o sub-arctic and
sub-tropical areas. The taxonm of this amciea still remains
unclarified. The earlier worker8 have reparted the existence of four
sub species, &. , dmestica (Linnaeus, 1758) , % (Macuuart I
1851), & (1851) and curviforcepa (Sacca and Rivosecchi, 1955) in
different mrts of the world. Hauever, the recent investiqations
suqgest that outside the Ethiooian reqion all M. danestica should be
reqarded as domestica inclr~dinq danestica, vicina and nebula (Patersen, 1974).
Bfological differences are a u m c t d to be present amnq
M. danestica population in different Dart8 of the world but it i s - - uncertain whether such differences are connected with mrpholqical
characters. However two identifiable sub species namely, M. d m s t i c a
cur~i forceps~ an endonhi lir: form and 5. domestics calleva Walker,
1849 (Y. cuthbertsoni: Patton, 19361, an exonhilic form have been
r m r t e d to occur in Africa (Keidinq, 1986).
me qecqraphical oriqin of M. daneatica wa8 alluded to be old
world and more s ~ c i f ical l v in the eastern Ethiwian rq ion fSacca,
1964). Thawson (1938) t r a r d i t 8 disnersal from Africa to hJt9De and
i t s invasion in the western hemisdrere was rewrted to be mainly
through the activities of man (Leqner and McCoyr 1966).
2. 2. Flier as we t s and their role in transmission.of diseases:
House fly i s of considerable immrtance to mankindr as a peat
causinq nuisance adding to the burden of ~eoo le livinq in m r
sanitatv conditims, hwnaers the qeneral improvement of hyqiene and
a l m discourages the m o l e from keeping a gooel standard of permnal
hygiene. Besides its role as a disease soreading agent, the c m d a of
f l i e s disturb w l e at the hours of s l e w or rest. I t s a m a n c e
a l m affects the rows and rduces milk yield in daiv-barna (Keiding~
1986 ) .
lhough the involvement of house f l i e s in the tranamissim of
h m d i r e w e had lonq been euswbed, only in recent times i t s role
in the transmission of diseases was well understad. l h q are seldom
ttue intermediate hosts of mthoqens but qenerally act as mechanical
carriers ( R o y and Brown, 1970).
Keiding (1986) r ~ m r t d that the house f l ies frequently
contminate eubstrates as well as f d , pick up pathoqens and
transmit by contact or throl~qh fly vomit or defecation. Experimental
evidences alsa suoaort that these wthcqens under suitable
cirmatances can infect animals and mn and effective flv control
had achieved a clear red~~ction in the incidence of diseases
transmitted by them.
2. 2. 1. Public health imnortanca:
Over 100 species n f vi~uses , bacteria, nrotozoan paraajtes and
helminth worms causinq various diseases in man have hen i.aolated
Fran house fl ies. However, there i s no evidence of cvclic develomnt
of any pathcqen in them (Hawnod and James, 1979).
The virus reswnsible for mlianyeli t is was isolated fram wild
caught M. danestica (Mnq and Glaser, 1943). In Texas U.S.A. I the
f l i e r were kncun t o be a mechanical carrier of poliamtelitis and
~ k m c k i c virusas (Melnick and D3Wt 1953: h-ancis &. I 1953).
08
The bacteria belonqinq to the genera Shigella, Salmonella,
Vibrio, Cmmylobscter and Myc~bscterium~ the causative agents of many - imDottant disealrcs in man are transmitted by M. h s t i c a (Iteidinq,
1986). Hawley $ &. (1951) rewrted the multi~lication of
Eacherisrhia * I Sa lme l l a achottamlleri and Shigella dynentriae
in fl ies. and Calliohora were capable of tranamittinq leorosy
causing pathogen from nasal rmlcus of an untreatd leprotmus mtient
t o perabna with ulcerative skin (Geatet, 1975). Chatterjee %&.
(1978) isolated ~ r a h a m l y t i u s from M. damnatica daneatica in
Calcuttar India. I n a villaqe of Thailand, M. dcmeetica was r e ~ o r t d
t o be r e m s i b l e for t.ranorni8aion of 5. s r Shigella so.,
Vibrio cholera Non 01 and V. fluvialis (Echeverria &. , 1983). -- Canuylchcter fetus juejlini ral~ainq enteritis in man was isolated
f m M. d m s t i c a collrctctrl from livestock holdings in %way throuqh
i t s link role in tranamiseion of the mthqen from animls to h m n
ford (Ro~ef and Kappenld, 1983). In Malav~iar n n t u r a l pooulaticn of
M. domestics was forind t o harbour E. &, Kleboiella pnemniae and - - S a l m e l l a ap. (Sulaimn 5 *. , 1988 a) .
Streptococcus ~hvoqenns, cnisinq i m t i q o ( inf l m t i o n of nkin)
in children was isolated frnm holise flv in Cairo, Eqmt (El-Tayab
c t s,, 1978). Forsev and Darorlqar (1981) ~howwl the shil i tv of - danantica to carry viable, ChlRmydin trachnmatia carlainq m. -
chlamydia1 ocular infections and trachma under f~vri~rahln
conditions. Based on a r a w ~ t u d v in Malaysia, Kan and Kav (1978)
remrtd the involverent nf t. domestics in the transmission of
P~eudomcsnas weudanallei , causing Meliodoais oresentinq as orostracia in tho eve of a wtient. l'he rickettsial. cathoqen~ Coxiella bllrnettii
causinq Q fever is remrtd to r m i n infective for the entire life
of flv and viable for 80 dava in its faeces and 90 days in dead flies
(Hucko, 1984).
M. dunestica is known to suread h w n intestinal motozoan - - oaraaitea such as Entamoeba histolvtica and E. coli (Roubaud, 1918:
Root, 1921: Connal, 1922). It is a l w rewrted to carry the cvsts of
Giardia intestinalis, Chilmatix mesnili, Wichomonas haninie and - T. foetus ( W o n and OtConnor, 1917: Root, 1921: Mocqon~ 1942). - -
M. danestica contributes conaiderablv for s~readinq the - - helminths to man bv mrrvins the wsta of ~invorm (Enterobiun
vermicularis) , roundorms (Ascario lwbricoides and A. scum) t whiworm (Wichiuris tricl~urcl), hookwons (Anrflostoma duodmalidae
and Necator mricanus) , tanatoms (w so. and Diwlidium m. 1
and stronqvloides (Narhu, 1969: Nadzhafov, 1972: G~~ota 5 1.) 1972:
~i~c?olu, 1977: Sulaiman g . , 19ABbl
The house fly I n ~ v ; l ~ h ~ v e heon reqardql RP causative aqnnt of
rhinitisl asthma, ollerqic: coni~tnctivitis 3110 oc'au~tional a l l e m
(Eluieaeret, 1978: Tee g., 1985). Its invnlvmlmt in the mviasis
of a ~ t i s n t with 1~ 11lrers and a lmronv ~ t i n n t with necrotic
tissue have a l m been reported (Leclerq, 1985: Shwe, 1987).
The fly control mtrilsnrcrs have shown to result in marked
reduction in the prevalenccr of diseases caused by Shigella and
Salmella (Lindbav g g. t 1953) I diarrhoea amnq children in rural areas of Uttar Pradesh (India) (Seqhal and Kumar , 1970) , typhoid, paratyphoid, opthalmic and bacillarv dysentery in Alexandaria (Eqypt)
(Mu1 Gawaad and Gayart 1972) , dysentery in Shemeen (Bulgaria)
(Takhirov, 1973) gastro-intestinal infections in Mexico state ( m a 1
Crozco and Garcia Martinez, 1982).
2. 2. 2. Role. in E~anamission -of -anirwl pathogens:
The involvement of 2. dmstica in the trammission of virus
causing hoq cholera (Mohler, 1919)t Colesioka mjundivae from
conjunctival secretions (Mitscherlich, 1943) and the virus causing
n w castle disease in noultry (Mileshev g &.I 1977) have been
reported.
Salmonella m l l o m , causing white diarrhoea in chickens
(Gesberich, 19521, Coqmebacteritnn psedotubereulesis, causing
ulcerative lymcharqit is nf horses and donkeys (Addot 1983) I
Streptecoccus aqalactiae , the agent of bvine mastitisf
Salmclla qallnaml the agent of white diarrhoea of chickensl
Brueclla abertus causinq bm~cellasis and Bacillus anthracis causing --
11
anthrax in c n t t l e a re known t o he t ranmi t t cd by N. danestica
(Ehriqht & g. 1 1987).
h e m e m a Dertenue, the callsative oqaninm of yaws is s u m c t e d -- t o b? t r a n a n i t t d by f l i t ? ~ mechanically (Castellani, 1907). The
oossihle tranamisaion of s w h i l i s amnq animals by the f l i e s has also
been r e w r t d by Kerr (1906). M. domestics is remrted t o be involved
in tho transmission of Habronema meqastcma and fi. muscae in horaes,
Ancylostoma caninurn in d w s , Rai l l ie t ina ces t i c i l los and Choanotaenia
infundihulum in m u l t r v (Werinde, 1976: Jaqanathan , 1980:
K a r u n m r t h y , 1988).
2. 3. Bionmics and behavior~r:
The developrental n e r i d of i m t u r e n of !. domstica is 0
remrted t o be 12 dav9 a t 14 C with a l m r and unwr temnsrature 0 0
l i m i t of 12.28 C and 42 C I r e s w c t i v ~ l v (Ghizdaw, 19751.
Cherrasterilant resis tant ntraina have been r e w r t d t o have low
fecunditv, low hatchahi l i tv , nrolonqd deve lomnta l duration and
shorter adult l i f e awn [Anaari, 1975). Dorinq winter, when the
a tms ther ic temperature in relat ively low, the manure with hiqher
tmperature favours the deve lomnt of i m t l l r e s in m u l t n t hcYdS~8
(Ani taqe , 1985a, 1985b). Lvwk and Axtell (1988) have tested a
simulation model of house f l y developnent in m u l t q manure. mouqh
hiqher moiature levels favoured ovimsit ion, it was unsuitable for
larval d w e l o m n t (Fatchurochim &. , 1989).
Cowell and Shorev (1975) s t t~died the courts hi^ behaviour of
M. danestica. Johnson (1976) r e n r d M. danestica on C o m r c i a l S o a ~ - - Manufacturer's Association (CSMA) larval rearinq mdim and found
tha t the f l i e s did not mate with the i r natural mwla t ion a f te r the
5th qeneration i n the laboratow. m e aqqreqation behaviour of third
instar larvae of M. d m s t i c a was found t o be influence3 bv m n i a
in the mediwn (Zvereva, 1989).
Schwf (1959) remrterl that the dispersal range of M. domestics
adults was 1 t o 2 milee and t.hev tend t o conqreqnte in areas s ~ ~ i t a h l e
for its feedinq and breedinq. In hiqh lands of Malava, the effective
dispersal range was estimated t o be 0.25 mile usinq radioactive 32
labellinq with P (Wharton s., 1962). The movemnt and
dintrih!~tion of f l i e s dacend on the weevalence of mul t rv fanns and
da i r ies which are the nroferred s i t e s for feedinq and suhsguent
braedinq (Lvnvk and Axtell, 1986).
The hanqinq objects are the oreferred s i t e s for restinq durinq
niqht time and the influence of various factors in the selection of
restinq olaces durinq tho hours of niqht have been discussed bv
Keidinq (1965). M. dcmestica adults exhibited a s w c i a l behaviour
tcuards new resting objects. The attractancy of a black plate in a
caqe decreased subsequently with time than the f i r s t introduction
(Mourier, 1965). Khan (1978) has studied the colour preference of
M. danestica and r e a o r t d the attractancy in the order of preference - -
black, blue, vellow and red. M. domestica females were remrtpd t o be
abundant and active in the i r f ~ e d i n q s i t e s durinq tho day t i m with a
m a x i m ac t iv i ty a t mid d w (Zotov and Fwlosov, 1983). However, R M v
(1981) has r e ~ o r t e d that the diurnal variation in the i r abundance was
m i n i m .
2. 4. Breeding habitats:
The house f l i e s have been remrted t o breed in a variety of
deeavinq, f e m n t i n q or rot t inq o q a n i c matter of animal and
vqe tab le origin. I t s breedinq has been observed from a variety of
animal manures includinq human excreta. The texture and mieture
content of dung determine its su i tab i l i ty (Keidinq, 1986).
The breedinq s i t e of M. domestica may vary fmm place t o d a c e
dep~ndinq on the availr\hj.litv of animal mnures. Breedinq has been
recorded in human excreta in orivy p i t s in Arizona (Schmf and
Silverly, 1954), in qarbaqe (Schoof g g., 1954) in f i e ld rottinq
melons and water melons d~lrinq sarinq in southern California (Lnqner
and Olton, 1975), in food s tu f f s of animal oriqin (Munzel, 1981)r in
the caged layer m u l t r v manure in South Africa ( H u l l ~ r 1 9 8 3 ) ~ in
wastes fran food orrxessinq industries ( I d r l984i)ae well a s in
aewaqe sludqe, under sui table conditions also from solid organic
wastes in open swaqe drains and seeoaqe it^ (Keidinq, 1986).
Preference of breedinq s i t e s has h e n found t o vary with seamnu
depending on the ava i l ah i l i tv of hreedinq medim. In Anand, ( India)
c a t t l e dunq was a favourable d i m throuqhout the year followed by
c i t y qarbage (Rabari and Patel, 1977, 1978), in Calcutta ( Ind ia ) , the
caw dunq was most a t t r ac t ive followed by human excreta (Joaeoh and
Pauri, 1980) and in Aanqalore (India) the oiq manure was most
a t t r ac t ive while c a t t l e mnure the least (Bai and Sankaran, 1982).
Ut i l i ty of w u l t r v man~lre fo r rearinq larvae of M. d m s t i c a
which i n turn used fo r feedinq chicken ae a source of p rote in han
been e x ~ l o r e d (Beard and Sands, 1973). The r ~ t i l i t y of M. d m s t i c a
puwe a s a feed s u h s t i t i ~ t e fo r b ro i l e r chickens has also been
r e o o r t d (Teotia end Miller, 1973). Fly larval infestation is the
chief factor for nitroqpn loss in c a t t l e dunq and its d ~ q r e e of
infestat ion determines the r a t e of n i t r q e n loss (MacrSue~n and
Beirne, 1975). Use of r. domestics larvae on oqan ic wastes in
bioloqical l i f e supmrt s v s t m s of smce c ra f t has k e n at temted.
Attemts were a l so made t o rear larvae of M. d m s t i c a t o diminish
h~nnan excrement and dronoinqs of J a ~ n e s e quail and were in t ~ ~ r n used
t o f e d the l a t t e r (Golrlheva and Erofeva, 1981: Coluheva, 1982).
Rams-Elordw 2. (1980, 1987) r e o o r t d tho nu t r i t ive vilhie of
M. d€B7WStir~ i m t u r e s and adul ts a s protein supulement with feedinq - - stllff f o r birds and reqardad them a s the aollrce of obtaininq anitMl
protein by recyclinq veqetahle, domestic wastes and an iml mnllre.
2. 5. Fly s m l i n q methods:
Various f l v n m l i n s methods a r e beinq used i.n assessinq the
malllation density a t different sitrlatinns. The choice of s m l i n q
technique mainly decenda on the b i o l w and hehaviorrr nf local
wnulationa. The c m n f1.v samoltnq methcds widelv used t o exaraso
the wpr~ la t ion denaitv a re f l v q r i l l count, baited t r a ~ q , spot cards,
s t ickv t rans and l iqh t t rans nf s m l i n q (Keidinq, 1986).
Amnq the three methds u8edl a rel iable index was ~ h t ~ i n e d bv
the s t ickv tape method in rnul t rv ranches (Anderson and Poorhauqh,
1964n) 1965). In sanitarv land f i l l s of southern California, the
Scudderls q r i l l , insect not and "D" vac were u a d and the q r i l l was
found t o be dependable (Dhillon and Challet 1985). Amnq the various
methcds used in mnitor inq f l i e s , the subjective index of cowlation
chanqe was obtained hv ScuMerls q r i l l , soot card and s t ickv t a m
count methcds (Beck and I m o r , 1985).
Turner 6 2. (1984) used a movinq s t icky t a w in c m r c i a l
caqecl layer hor~ses and cornred it with saot card method. The atickv
tape method qave additinnfll information on two other f l y swcies
(Lysvk and Axtell, 1986) and was useful in mnitor inq the seasonal
trends in s m t i a l d i s t r ib r~ t ton of house f l i e a and s table f l i e s a t
dairy f a m and n wstr lre in central IWA (U.S.A.) (Black and
Krafsrrr, 1985). Of the seven adheoi~res evaluated in stickv t r a m ,
"Hwia 200" wfls r e o o r t d t o he an ef fect ivr atlh~ni v r fnr t r a ~ i n q
f l i p s (Sirlaiman g. 19R 7 ) .
Sento and Suenaqa (1970) used baited t r a m with a ha i t of
rot t inq f i sh and "takja" in a Korean farm house. Lvsyk and Axtell
(1985) used a juq t rap with "Golden Maldrin" h a i t and pnintwl with
yellow colout found moRt sui tahla for f l v at t ract ion in caqed ].aver
wultrv houaea. Pickem and Thimi jan ( 1986) eval~lated the eff iciencv
of UV as l iqh t eource in the tcanq. The f l v pooulation estimati.ons by
m r k release recaotr!rs methd with fluoresrent a t i l i n a l substance or
phenal.ohthalein were nlnrn sllitable than conventional pooulation
estimation methods (Postnchil and Brqach, 1982: Krietiansen ~ n d
Skomnd, 1985).
2. 6 . Population dynamics:
The pornlation dynmics wa8 studied from the seasanal chanqea in
the natural popr~latirm of E. daneetica. Linhares (1981a1 1981bl
determined the anthmwahil i c index, seasonal abundance and
hrl iophi ly of synanthrnoir f l i e s from urbnn, rural and natural
environments in Camoinas r i t v (Brazi l ) . Niyazova & &. (1983)
studied the index of abundance and percentage orevalence fo r
M. domestics and other aqaoriated f l i e s and remr ted the chanqes in - - svnanthrooic behaviout nf f l i e ~ in an Eurowan c i ty of USSR.
In the livestock farma of Hawaii, M. m s t i c a was more sbvndmt
and i t s distribution was qoverned by various limitinq factors of the
animal manure (Toyma and Ikeda, 1976). In Narlkkaa (Niqeria), the
distribution wtterns and 8ea.mnal chaqes have been studied (Iwuala
and Onyeka, 1977). In a villaqe OF Orisaa (India), i t was six timer
more abundant in an earthern kitchen with m r sanitary conditions
than a concrete kitchen (Red+, 1981). In Jalnaiquri (India) , its
distribution wae mainlv qovernd by a variety of bredinq media
available (Paul &. 1983).
The influence of matrnrolcqical factorcr on the aeamn~l
abundance of house f l i e ~ ha8 heen r e t n r t d f r m the follovinq
ntudies. The density of holl~e. f l i e s has been correlated with relative
huniditv in Egypt (Hawlev G., 1951). The c l imt ic condit iona ~uch
as rain f a l l , relative hi~miditv, maximum temmr~ture were correlated
with abundance in livestock farm4 of Izat naqar (Khan and Patnaik,
1978). The results of the ~rarious studies conclude that the wak fly
nbundmce varies in different nlaces durinq monebon seaebn at Gauhati
(India) (Miranouri and Lahkar, 1980), the sorinq and autunm determined
by the t-rature and relative humidity in Samsrkand (USSR)
(Svchwskaya, 1962) md a hiqhest wak of abundance durinq m ~ b o n
nnd m l l e r one in aost mnshon period in Dacca (~anqladeah) (Ameen
and HUQI 1973).
While studyinq the cowlation dynamics of house flies Weidhana
and L a B r w e (1970) recorded a rnaximm three fold increase of house
fly index. Howaver, a similar study carried out in north central
Florida revealed a rate of increase of w l a t i o n , which wan leas
than one to six fold in R qeneration (LaBrecque %&., 1972).
Lineva (1953) and Anderaon (1964) developed methods for
distinquiehinq n u l l i m r o ~ ~ ~ from Darous flies for estimatinq aqes of
cyclorrhnaous di~tera. The criteria for classification were the
mesence of follicular relics in the ovarioles, oedicels and lateral
oviducts. The other criteria em~loyed were the Dresence or abaence of
meal fat bodies, the nvmher of tracheolar skeina in the ovarioles,
the n h r of functional ovarioles and its cammctness. Krafsur
(1985) demonstrated a n w method for age qrou~ing of field collected
diptera haad on the staqen of developnent of ovarioles and
calculated the survival rate nf M. dcmestica in different months.
2. 7. Laboratory rearinq:
M. daneatica was remrted to be easily reared in the laboratory - - became of its manurabilitv and ability to ~ro~agate in a widely
vnwinq conditions. The various rearinq method8 which sliqhtly differ
from each other were selected through choice of factors such as
W c e , money and the nrnhr of insects required. M. &nestica larvae
was reared using horee manure, horoe manure and additiveat cow
mrmre, cotton wool mds soaked in diluted milk and on f emnt i rq doq
biacuita ( S c h ~ f t 1964).
Schoof (1964) ha8 also reviewed the varibus kly breeclinq media
develooed by various workers with available local inqrdients &. , CSMA medium, mA medim and coconut o i l c ~ medium. The other media
widely u s d for f ly rearinq include wheat bran, glucose, yeast and
water (Gera and Guuta, 1975), conditinned CSMA medim (Bryant and
Hall, 1975), hqasse with water (Bridqer ,t g., 1984) a d a larval
diet ccmposed of wheat bran, yeast and mter (Charles g &.t 1987).
The choice of brnedinq media depends on faater &velopnant, qrnater
dngree of eynchronization of o u ~ t i o n and increased pvml wiqhts.
Adults were maintain4 in laboratow on a variety of feed auch
as milk oovderr water and sliqar (Harrison, 1950), fresh ripe bananat
cane suqar, milk wuder, aqar and water (Deoras, 1954), milk and
suqar (Sinha, 1974) and qlumsn, condensed milk and water (Gera and
Guota, 1975). Keidinq and Arevard (1964) described a rearinq methdl
for house f ly without thp Lnas of qenetic viqour. The larvae reared
in four different avnthetic media have shown significant differancea
in the body veiqht, protein, carbohydrate and linid contents but not
in a& and water content (D~ahmlkh, 1980).
2. 8. Ply control:
A l o g term f lv control can be achievd by e n v i r o m t a l
eanitstion. Ihe chemical control mnthcds, thouqh yield quicker
effects can only be a s u m l m n t to the environmental measures. The
environmental sanitation includes the elimination of fly brecdinq
sources, exclusion of f l i e s from wtential bredinq sources and bv
killinq larvae in infested materials (Busvine, 1980).
In rural areas of Tr~diana, M. domstica breeding has been
auccessfullv controlled i n tomato cannerv waste water laqoons bv
usinq a wlythene cover whi.ch wa~ also cast effective (McCoy, 1958).
In poultry ranches of northern California, f ly control hv manure
management measures were shown to be cant effective (Rrlrton ,t &. , 1965). In Danish farms, the aanitary meaRures of fly control hold
good but difficult to nractice due to lack of farm labourers
(Aeidinq, 1975). In sanitarv land f i l l s of Haw8iir the soil cover of
leas than 25 m thickness did not prevent the emergence of f lv
i m t u r e a buried underneath (Toyma, 1988).
The experimental fly control with insecticides waa more
effective than mechanical measures such aa mud ~laeter inq , coverinq
with sand or tarred cloth etc. (Pradhan 5 &,, 1961). Keiding (1975)
has studied the feasibility of f ly contrbl in Danish f a m by usinq
chlorinated hydrocarbons, various orqan&oephorous c-unds and
uyrethmids. The residual spray on resting surfaces was the most
effective and the other measures such aa restriction of residual
emray t o 30 or 10% of the spravnble surfaces, innxegnated ribban81
toxic m a r baits minted on strateqic placesl non reaidual suray and
ccmbininq M e r a t e use of a toxic bait and unrelated larvicide were
also u d (Keidinq and Je swrmn~ 1986). The insecticidal control of
M. danestica and other associated dunq breeding f l i e s in animal - - manure increases the ~rod~rct iv i tv of &fry and beef catt le (Earnestt
1986).
Rcqoff & &. (1980) have studied the r amnse of male
M. rhmestica t o "nlocnlnre", a cheromane and to conlsinations of - - various branch chain saturated hydmarbons with and withrn~t
m~rcalure. The attractancy to dimethaate~ allethrin and fenvalerate
but r-llancy t o methoxvchlar and cyphenothrin by M. dunestice has
been reparted (Rani and Rsmnit 1984). Treatrent with cymmyzine wan
the mot awt effective in caqed layer pooltry houses. Larvicidinq or
adulticidinq with dimethoatel fenthian and dimthoate, oennethrin,
dimethoate and stiroohos achieved f ly control i n a mxlerately cont
effective manner. Earlv removal of manure befdre teak mamh of the
f l y conlsined with more selective insecticide use m l d provide an
effective f ly control (Keidinq, 1986).
Cattle dunq treated with 0.35% triflubenzuron a t the rate of 2
1 l / m has prevented the de~ralomnt of M. danestica egga and its
wttncy r e k i n d for 3 days. mird instar larvae treated with 0.0035
t o 35% of triflubenzrlron produced defonned w w r i a (SZabova and
Z a j n ~ , 1987). The wridvl ether, an insect qrowth r e q u l a t o ~
ccmmnd haa becn studied aqainat M. dmatica larvae resistant to
cyrethroid and oqanmhosohorous ccmaunda in laboratory (Kwnda
et &., 1987). Innecticida resistonce of M. dcmestica to crotoxyohoa, - tetrachlorovinphca, dimethoate, dichlotavoa and oennethrin has been
rewrtd in New York dairies (Scott 5 g., 1989).
The svneqistic effwt of neem and custard awle extracts has
been shcm to be as toxic as DDT to M. dcmastica (Qadri etg., 1977). Extracts from leaves nnd air dried root8 of Cathoranthua
~lkal0idS induced siqnificant levels of sterility in males and
females of r. danestica and the leaf extracts were found to be m r e effective than mot extracts (Sukumer, 1987).
The effectiveness of electrocuting liqht trap with black liqht
( W ) wan incrwsd bv addinq "musealure" in the control of flies and
the n W r of flies tram& was mainly de~endinq on the w l a t i o n
size of flies in caqed laver w l t r v houses ( S k m n d and Mourierr
1986).
2. 9. Natural enemies of Musca dcmestica:
A rich variety of natural enemies y&. predatorsr parasites,
mthoqens and parasitoids attacking almst all stages of H. dmstica
life cycle has given amle scope for identifyinq and selectinq
neptoeniate biolcqicnl control aqenta. Majority of them are
the coexisting invertebrate fauna which olay an imctant role in
rcqulating its cnpulation, demite its e n o m s reorcductive
potential. It has been emhasized for the continued efforts in
maintaining these agent^ so an to utilize them for develooinq an
inteqrated control strategy. The multi agent awroach with a
judicious cdination of aqrints during an amrowiate develomntal
stage of host mav yield a successful control (Axtell, 1986b). an
integrated fly control otrateqy by emloyinq Macrochsles
rmscadanest icae and FJscuroaoda vegetans aqainst eqqs Bacillus
thuringieneis and Neoolcctana camaoaae against larvae and miaoned
baits of naled or fenohloronhrm aqainst adults in multry houses has
been demonstrated and ~ r o v d to be effective (Wicht and Rodriquez,
1970).
2. 9. 1. Predators:
l'no Dredace3u.s habits of dunq infeatinq macrochelid mites on
house fly eqqs have been remrted by Axtell (1962) and Rcdrjquez and
Wade (1962). Prevalence of 2. muacadanesticae, Fuscuropcda so. and
Glwtholapis confusa in mjltrv drowinqs of northern California has
been reported (Peck and Anderson, 1969). Cicolani (1979) studied the
intrinsic rate of natural increase of 7 swcies of macrochelid mites
ordating M. danestica eqqs. Predatory and disoersal behaviour of
M. nuscsdomeaticae, G. confusa and Poecilochirus deutronwrohs and - influence of moiature content and aqe of the manure have a l m been
studid (Gedcn and Stofflolano, 1988: Geden g. t 1988).
me inported f i r e ant Solenods geminata has been shown t o hava
a high degree of ~redatorv rntential by feeding house f ly egqs cYrd
immtures i n garbage bins (Pirnentel, 1955). The social soider,
S t e q o w u s miroearm Paveri had bwn introduced in domestic and
per idmet ic habitats of South Africa winq i t s predatory behaviour
on adult house f l ies . T h i ~ aaider ia harmless to man and capable of
withstandinq starvation fnr a long wricd. A awctacular control of
house f l i e s has been ach1eve-I by th is awcies (Stem, 1959). The
predatory potential of Labia ininor an eawiq on l io~~se fly eaqs and
larvae along with i t s l i f e cycle has been assessed in tentperirte zones
of Demrk (Mourier, 1984).
Prtchinsky (1913) reviewed the predatory activity of other dunq
breeding diDteran larvae on house fly larvae. The black qar+aqe flv
leucoatma has heen rewrted to be a nromising biolnqical
control agent of n. d m s t i c a and other nuisance f l ies in multry
Mnure (Andernon and Poorbauqh, 1964b). The fleasonal abundance of
predator wpulatims of Muscina atabulans And 2. leucos tm have also
been studied (Peck and Andernon, 1969). Oleckers and Hullw (1984)
have demonstrated the u t i l i ty of g. camesis lamae in the control of
house f l i e s i n multry manure in situations where the n m b r of other
manure breading dipteca are low. Under manure managmint practices in
caqed layer f a m , a aiqnificant reduction in house f ly woulatim
h~ been achieved with increase in natural enemies ( S h e d , 1983).
B r d i n q of M. danestica in pits of enclosed poultry houses has been
disolaccd by E. aenescena durinq a wriod of 18 weeks when the latter
were all& to breed without any restriction (Noalan and ~ i a b m ,
1987). The= studies revealed that oredatory dipteran larvae, the
adults of which do not cause any nuisance to men, may be used in
controlling house fly m~ulation under auecific habitats like wultrv
farms.
In Jawat Sumatra and South Africa dung k t l e s belonqinq to the
familiest Cooridae and Histeridae are known to control hoi~se fly
imtures through their predatory behaviour (Sinmundst 1940). Leqner
and Olton (1971) cornDar.4 the ~redatory ~tential of adult beetles of
Lahidurinae, Histeridae and Staohylinidae in domestic anirnal mnure
f m various zoqeoqraohical reqions of the World. Carcinopa ~umilo
could succeasfully be mintained with a diet af frozen M. dancstica
eggs at various density levela. The predatory capacity of males,
femlea and larvae of this swcies at various density levels alonq
with its daily rate of increase of it8 -lation has been studied
(Mocqan & &. , 1983). 'his wedator is knm to concentrate on the
surface region of the manure (Geden and Stofflolam, 1988). In South
Africa, E. trcqldytes f om la ti on is nbundant which effectivelv
checked the fly br&inq in multry manure (Hulley and Pfleidrrer,
1988) .
2. 9. 2. Parasites:
Imnaturea of multi-insecticide resistant strains of M. damentica
have been tested for their susceptibility to parasitic nematdes such
as HeterorhaMitus helithidis and Steinernem feltidae and the lat ter
nwcies was found to br, more vinllent resulting a higher parasitism.
6aaed on these studies, it has been suggested that S. feltidae can be
used as a supple men tar^ measure in the contml of house f l i e s (Renn
e t al . , 1985). --
2. 9. 3. Pathogens:
M. domeatica latvae have been rewrted to be sus~eptible to - - wettable d e r fomlat ions of 8. thurinqiensis. Hawrver no adverse
effect ha8 been noticed on adult f l i e s ( Al-Azawi and Jabbar, 1989).
hung fungi, h p e q i l l u s 9, Beauveria globlifera,
0rqxsa mricana , . qryll i , E. mscae, E. aphaeroeuem and Fusarium -- m e have been reported to h mthcqenic to M. danestica (Charles, - 1941). Release of frenh mycelia of E. in f ly infested olacea
has been s h m t o cauae mortality of adults and this aathoqenic 0
funqus developed well at 20 to 25 C (Vcqel, 1968). Field studies
have shown that nycasis caused hy th is funqus i s mainly influenced by
the relative hwniditv and drv ml seamn is the most favourable for
its infratation (Kramer, 1981). Mullens and Rodriguez (1985) have
studied the dynmics of E. E, conidial discharqe frun
M. danestica cadavers a t various relative humidity levels. The - - incidence of infection of this funqus increased when infected house
f l i e s were released into the wild wpulatian (Kramer and Steinkarus,
1987).
The term parasitoid was f i r s t coined by Reuter (1913) to
describe insects that develop as larvae on the tissues of other
arthropods (usually insects), which they eventually k i l l . Adult:
female parasitoids foraqe actively on haste and deposit their eqqs
into, over or near tho host individuals. U w n hatching, the larvae
w i l l feed on host tiasues and complete their developnent either aa an
ec tbo r endoparasite. Solitary parasitoids develop einglv i n or on
their hosts while grnqarious s ~ e c i e s develop in groum from eqqs laid
during one or more otrimsitions. Parasitoids thus differ from tnre
predators which have free-livinq larval staqes and normally require
m r e than one prey item to conplete their develounent (Hassel and
Wave, 1984). Amnq the various natural rqulatory agents of diuteran
f l i e s r the parasitoid warns attacking the puwria received
mnaiderable attention in recent times (Axtell 198& Sunreya have
been carried out world wide to find out the regulatory mle of
parasitoids in various countries (Leqner and Olton, 1976).
2. 9. 4. 1. axo on any of m~wl wrasitoids:
The p a r ~ i t o i d wasos belong t o different families such as
was m a x i m during t h e s u m n r and t h e tic-soon month and
d i s t r i bu t ion o f P. vindemniae has been recorded in a l l hab i t a t s
(Srinivasan and Balak r i shn~n , 1989).
2. 9. 4. 3. Biology and behaviour:
Studies on var ious a s m s of biolaqy have been ca r r i ed art i n
w r a a i t o i d s . Roy 1. (1940) s tudied t h e bionanice of
D. cdchycenllr. Its d e v e l o m n t s l d u r a t i m v a r i e s from 20 days in - s m r t o 45 days i n winter i n t h e host M. dunestica m w r i a . Bull
(1982) has ahom e iqh t recoqniznble s t aqes i n cia vi t r ibenn i r
mtmcqeneais . A t hiqh t-ratures, t h e product im of males i n
thelytokous M. m i r a p t o r was t r iqgered due t o t h e blockage of
endomitosis and fonna t im of d ioloid female producing eggs ( L e p e r ,
1985). Umlqis m f i a s hae shown a f a s t e r r a t e of d e v e l o m t and
hiqher i n t r i n s i c r a t e of q r w t h am! fecundity but t h e .sex r a t i o did
not vary s iqn i f i can t ly with mother's aqe o r t e n a r a t u r e (Smith d
Rutz, 1986, 1987). Arellano and Reuda (1988) have rsoor ted t h a t t h e
develapnental d u r a t i m of 2. eqg and its f i r s t , second and
t h i r d l a rva l i n s t n r s ranqc f m n 20-50 hours, 2 4 days, 2-3 davs and
2-3 days re-ctively. The DTFDUOFJ period l a s t s fo r 1 day and cum1
period ranqes f r m 6-R days. A t higher t m r a t u r e s , 2. & haa
o h m a reducticm in t h e averaqe i m t u r e d e v e l m n t a l duraticm
all and Pischer, 1988). Fran a laboratory study, t he l ~ e v i t v
(32.5 davs) , fecundity (127.3 eqqs/fcmale) aml host feeding behavibur
of g. himalayanus have been rmrted (Srinivasan and Panicker, 1988).
Rsmmal idem , Braconidnet Ichnemmidae , Encvtidae, Eumlidae,
Dimriidae and Chnlcididae ttnder the Suocr Fmilv Chalcidoidea (Order
Hylr*moaCera). The fanilv P t s m l i d a e camrims the l aqea t nudxr of
oarasitoid w a m attadcinq f ly w r i a and includea the i m c t a n t
oara~i to id g m m viz. Swlmqia, MuscMifurax, Pachycrmidwa,
NaMnir and Urolcois (Leqner 1. I 1975: Reda and Axtell! 19854 .A
siblinq sceciea of $. has aleo been rewrted fm Auntralia
and has a ccnplete reproductive iaolatim with the form distribvted
in NH zealand (Leqner, 1983). The cytolqical studies of
D. himalayanus have s h m that i t s diploid c h ~ n h r of 10 - (Analin t g., 1987).
Leqm?r and B w n ( 1966) recorded 14 soecies of parasitoids
attackinq hmae fly oumria fm various collection s i tes of Canada,
Chile, Cmta Rica, J m i r n , Trinidad, U ~ J U R J ' and [J.S.A. b i n q
1962-1965. In the western hemimhere the nuher of parasitoids were
~ r a t i v e l y less than oos t rn hemisphere. The Swlangia m. were
accounted for a hiqh d-rw of natural mraaitism i n northwestern
U.S.A. (Leqner and Mew, 1966). In Southern California multry
rmhes, M. and 2. a were r e w s i b l e for a maxim
oaranit ic activity ( m e t g. , 1968). In eastern hemihere and
Pacific islands the m l v distributed mraritoids vere k n m for n
hiqher activity. But the fnma restricted to eastern harnimhere alone
play coawratively a Ie-r role (Lclqner and Olton, 19681. m q a n and P a t t e r m (1975) studied the natural mr~itism of wild pcmlatim i n
a mine farm a t Florida. In Hsvaii animal f a m , 14 e i e s belonqinq
t o the fmnilies P t e m l i d a e , Encytridae, D i a ~ r i d a e t Cbalcididee,
Cyni~idae and Stachvlinidae were k n m t o attack the dung b r d i n q
f ly m r i a and of these, S. endfun and S. csmemni vere the met
abundwt (Toyam and Ikda , 1976).
In India, onlv a few stldien are available on biological control
aqenta of munmid fl ieo &.mite the acute woblem due to f l i e s and
fly-barne diseases. Rov and SirMons (1939) l i ~ t e d the parasitic wema
viz., Spalangia sw., Bradlvreria fulvitarsis, 8. argentifrona and
Dirhinus wchycerus nttackinq the pumria of musmid f l i e s in
Calcutta. S h a m (1971.) stlKlied the bioloq~ of Muscidifurax
mraaitizinq tmse 1:lv twmria. In Bangal-ore, tho fnllbwinq
mrasitoids vi2.1 5. wr 2. niqroaenea, 5. e, 5. M, P. vindmniae, Ditrirhinot halmis sargusmetallintrs, g. pechvcerus and - D. sp. nr. infiena have twen recorded from dipteran puwria breedinq - in bavine mnure. Munq these m c i e s , 2. c~rmeroni was the minr me.
However, the denaitv of these native parasitoids was not sufficient
t o check the fly hr&inq rffectively (hi and Sankaran, 1977:
Sankarw 1980). D. mchycenm has heen recorded flnm a
multrv farm in Tiruchv (Kamnrmsarthy and Naqarajan, 1986). In
livestock fama of M i c h e m y , P. v i n d d a e l 2. ~ w I ) ~ W I ~ I
g. n i g r m and g. himalavnntm have been (yc6rd.d and their d e ~ i t y
I n a study on the woference of parasitoida on the house fly and
rtable f ly host wonria, Morqan & &. (1979) shcued the preference
of E. with M. dunestica than Stamxys calcitrans. Its
paranitic activity war also influenced by the host mrasitoid ratio
and hmt q e . The develomntal duration of !. and
S. drowDhilae was shorter ir! Hamtobia irr i tans than 2. calcitrans - 0
or M. danestica w w e at 27 C (Camhart & &. , 1981). 8
Musciditurax am. and S w l q i a sw. did not exhibit any preference
wer the puparia of stable f l i e s and house f l i e s i n nature (Meyer and
Petersen, 1983). P e t e r m 2. (1985) have recovered U. m f i ~ e s
fma the house f ly and stable fly w m r i a i n eastern Nebraskan animal
farm i n U.S.A. In an east central Texas wsture, the D I I W ~
mrasitoids attackinq f ly oumria in bovine manure have a broad
mectnnn of hosts (Rlume, 1986). From a laboratory studv, it was
evidenced that 2. niqrA did not show any preference when both house
f ly and stable f ly wmr ia were offered a t the seme time (Hall and
Pischer, 1988). However, the fecundity and hnst destruction potential
of S. endius differ with 1. h s t i c a and Chrysomyia meqaceohala - w m r i a in the laboratory as the f o m r was found to be more suitable
for otoqeny ~ t d l u c t ion ( Arenello and Reuda, 1988 ) .
The occurrence of suwrwrasitism i s due to the suwlv of hosts
i n -1 or less nmkers than the maximnn attack rate of mrasitoid.
Sucer m r a d t i m of 1. vitrioennis on N. danestica w ~ a r i a resulted
i n the reduction i n aurvival and adult size. We proportion of f w l e
p m q q war aim reduced but it had no effect on the rate of
omplrticn of devdoanent of the wrmitoid (Wylie, 1965). T g r m and
Ikda (1980) showed that at animal farm of Hawaii, sucewrasitiam
due to I?. taptor, g. luzorenaia and Encoila impatients were
r e m r i b l e for the high incidence of non-viable fly puparia. Prow
and Morgan (1983 a 1985) r-ed that the eucewrasitism due to
S. endius resulted in the reducticn of its reproductive potential in - - mcla release DrograrrPnea.
Multiparasitiem of 2. and M. ramor on N. dwoestica oume
reveals that the f o m r swcies tends to avoid oviwsitinq in Dume
mraaitized by the latter whereas the latter did not avoid wcae
wrasitizd by the former (Prom and Norqan, 198261.
Studies on caroetitive wrasitism between E. zaraptor and
U. rufiw8 by e m i n q the host puparia sinultaneously to both - - parmitoids have shcun that the former was more efficient in
mrasitizirq house fly w m e than the latter (Pawson & g., 1987).
The intra-aoecific larval oxroetition of N. vitrimis,
jl. and S. camoroni has been studied and the n h r of larvae
found develwiq wao 2.5, 1.0 a d 1.0, rewctively. Larval crodinq
in jl. raptor and S. cmrnni unlike N. vitripennis does not affect
the aex ratio of the survivors (Wvlie, 1971).
-el and Pimentel (1963) studied the habits of dispersal and
6.nsity relationships with 1. vitriwnnis and E. d m s t i c a and the
fad f o m signif icantlv disoersed faster than un fd ones. Leqner
(1983) atudied the matinq and foraqinq behaviour amnq various
crtraina of M. raptor. The house f ly larval breeding medium with a
duwity of 25 larvae w r 100 'gran d i m elicited siqnificant
reawnse by the mrasitoidn as evidenced from olfactaneter (Soafford
e t al., 1984). --
2. 9. 4. 4. Reproductive wtential:
m e reproductive wtent ia l of the wrasitoids i n me of the
i m r t n n t parmeters in determininq their success as a bic-control
aqent and has been studied by various authors. Hybridization of
mrasitoids fran climatoloqically similar and geoqraDhically isolated
areaa could incream their rwrcductive mtential. The inundation of
exotic strains could omduce suwrior strains through intercrass
(Leqner, 1972). Morqan 5 g. (1976ri have reoorted from a laboratow
study, E.1 uniraotor m d s t i o n multiolied 55 timea in a generation.
Reduction in the developnental duration of 2. niqra has been observed
a t higher t-ratures and a t various host d e h i t i e s but the
~ r a a i t i s m has declined (Hall and Fischer, 1988).
Ablea 5 1. (1976) studied the develomnt of S. endius and
M. raptor' i n relation t o m s t a n t and variable temaratures and also
&velo#d an algorithm t o p r d i c t the develoanent of parasitoids bv
providinq 8 i ~ l a t i C n of reswnaes to constant and variable
tameraturea besides a hiqh correlation coefficient obtained between
orndicted and &awed develomntal rates. Morqan 6 &. (1976)
estimated the daily mortality ra te of S. endius as 0.3315, daily
w i m i t i o n rate as 9.46 eqqs w r female and the average n m r of
prcqeny emeqed wr female wr day as 2.6.
Legner (1983) st~ldied the fecundity and cold hardiness m n q
M. rapfor straina a t hiqher host-oarasitoid ratio and ohserved that - the females produced lesner female oroqenv. The difference between
the oroqeny prcductim and host oarasitization i s known as the
m r m i t e induced mottalitv and it increased with t m r a t u r e . The
nnctality due to th is ohenmenon was significantly hiqher than
m r m i t i m in g. m f i w s (Mathevs and Petersen, 1989).
The pupal size had a orofound effect on the wrcentaqe
mrasitimn and ~rogenv ~ m d u c t i m in N. vitriwnnis, a greqarious
oarmitoid of E. h s t i c a (Nagel and Pimentel, 1963). When the
infected ouwe wnre e m e d t o low temceratures, there was an
incrmm i n the raomductive wtential of M. raptor and M. zacaptot
and the l i f e scan a s well as prcqeny pmduction in S. endius. The
w r m i t i c species may be imroved for use i n biological mntml
woqrmmnea through cold storaqe techniques (Legner, 1976). The mass
culturinq methad8 of 5. + suitable for inundatinq f ie ld
relemea 'were develomd ensurinq the production of one million
oaradten w r week (Morqnn et1.1 1978). The frwze killed M. raotor
m m r i a have been u s d for the m s s ~roduction (Peteraen and Mathws,
1984). The utility of irradiated and cold stored house fly pumria
for expMure to parnsitoids ~ l d colony maintenance have a1.w been
rearrted (Morgan & g. 1986).
2. 9. 4. 5. Host wrnsitoid interaction:
Host parasitoid interaction has been studied from the
reproductive and develounental r e m s e of mrasitoids. New York and
Florida strains of M. rkxwstica pume with different nutritive
qualities genetically ahwed variations in mrasitization and Drqenv
om8uctim by N. vitrimnnis. The wrasitoids have also exhibited
difference in their life table mrameters and cooulation qr0H.h
characterist ics (Chabsrnl 1970a) 1970b).
Olmn and Pimentel (1974) recorted that M. domestics under
interme selective oressure by N. vitripennis declined in its oroqenv
moduction and looqevity in 40th qeneration. Tho develomnt af
resistance by M. dcmestica to 2. vitripmnis in a laboraton,
hont-paraaitoid syntm reduced the succeen of the wrasitoid.
M. danentica a l m exhibited a decreased tendency of oscillationsr a - - reducod mean m a t h size and a reduced variance krt an increased
logarithmic varinnea (Pimentel &. , 1978).
36
Zsreh &. (1980) studied the evolution of host-wrasitoid
systan rarder laboratory conditions and thereby the population
kinetics of m. danestira and 2. vitriwnnis. In the f i r s t 20
generations no difference could be detected in mean M. danestica
density. However the adult cawlation was reduced thereafter and this
trend continued for 50 qeneratims.
Weidhaas &. (1977) constructed a computer simulation d e l
f m the l i f e history mriimeters of M. domestics and S. endius which
can be successfullv awlied to study the i m c t of parasitoid
releases on the reduction of house f ly density.
2. 9. 4. 6. Sampling methods:
Rutz (1986) has reviewed the various methods for monitorinq
m r ~ i t o i d s and their relative merits and demerits. The puml
collection method indicates the relative abundance but it i s beset
with the ~rrzb1e1-11 of hrzsts of variable aqes. The other methods y&. , emerqence trap, mpal t rap and sentinel a lwe monitoring qave the
b i n d result. cuinq t o variable wpal densitv and loss of srmoles.
The rtudies have been carried out in the dairies and enclosed multry
h a m s of esntern Nebraska and north Carolina dairy, beef , multry
mine and sheer, huminqs using more thw one method of estimation of
natural parasitism and the merits and demerits of each methnl -re
d i e c u e d (Myer and Peteraen, 1982; Reda and Axtell, 1985bMerchant
et al . 1985). --
2. 9. 4. 7. Population dynamics:
In Danish f a m , the ~ a r a s i t o i d s were lees during the early f ly
aeamn which i n c r e d steadily with a peak in October (Murier ,
1971). The influence of t m r a t u r e , hmiditv and depth of mnure on
hocrt destruction and fecundity have been studied and shown that the
Smlangia scp. c m i s t e n t l v wnetrated t o a greater depth (Legner,
1977). In Nebraska (U.S.A.), during winter its emergence was
increaad and abortive carasitism was also decreased sharply due t o
the non occurrence of diamuse (Peter.sen and Meyer, 1983). The
m r ~ i t i s m of U rufioes was hiqh during October in outdoor habitats
(Smith and Rut21 1985). Petersen and Pawson (1988) have studied the
l a t e seasonal act ivi ty of M. raotor which showed a high incidence and
emergence levels and 2. declined during cooler mnths but
Spheqiqaster 3 was abundant throuqhout the release ~ e r i c d in
liveatock confinements of eastern Nebraska, U.S.A.
In caqed layer w u l t r y manure of southern California,
M. =raptor, M. raptor and S. ciuneroni were the mast abundant and - - - - M. zarapter and 2. cameroni were primarily diurnal in the i r - -
I &arching act ivi ty (Mullens & g., 1986). In Z i n h h e ,
Smlanqia sw., h i c h o ~ r i s and Nasonia scp. , the indiqencus
nntcnqhsgous insects were k n m t o attack the dung breeding dioteran
wpae (Harris, 1987). In enclosed shallow oit egq layer m u l t w
houws of north central Indiana (U.S.A.), S. cameroni wvas the m a t
abdmt species followed by 2. niqroaenea, S. endius, 2. niqra,
N, v i t r i m i r , M. MIA Maeneta d l i w a (Merchant &. , - 1987).
2. 9. 4. 9. Fly control with mrasitoid releases:
The earl ier efforts to control M. danestica and other dung
breedinq f l i e s by using bioloqical control agents were attem~ted i n
ceztain Pacific Islands. In Hawaii Islands amnq the 16 soecies of
hymenoDteran and coleo~teran natural enemies introduced since 1909,
tmlve got established and ~mduced encouraging results (Leqner,
1973). In Fi j i curd Gaun Islands, the introduction of S. camerrmi from
Hawaii in 1930s had achieved a siqnificant f ly reductim (Vandenburq,
1930; Simnds , 1958).
In California, the introducticn of mrasitoids to conbat dunq
k. .d inq f l i e s cannenced in l%Ost by releasing several exotic
mncier/ strain6 of TachnMhsqus zelandiua and five species of
Huacidifurax and 5. cameeonit 5. endiust S. niqroaenea and 2. niqra
i n dairies and poultrv ranges. The released oarasitoids differ in
their tolerance t o temeraturr, humidity extremes and i n their
frcurdityr longevity and ~r0binq abil i ty (Moore and Legnor, 1911 ).
Sphrqigaater sp., imoartd fmm South Africa was mss released but it
failed to establish i n the California mrasitoid aatolex (Gerinq and
1968). Aleochara t a n i a t a , a S t awl in id from J m i c a ha8
k.n liberated i n c-tnl southern California but the results were
not available. Inoculative releases of T. zelarxlicus, S. endius and
M. raptor carried out i n an enclosed wultw house in southern - - California revealed that T. zelandicus was m s t effective (Lqner,
1972, 1973: Olton and Leqner, 1971).
Comnonwealth Institute of Biological Control exwnded the
mrasitoid release activit ies to West Indies, Mauritius and m r t s of
Asia. Various studies were a lm carried out in this field in Chile,
E l Salvader, Mexico, New Zeland and Pacific Islands (Lqner and Bay,
1970). In Danish ca t t le farms, 2. cameroni and M. -were
mbjected t o inundating releases durinq early fly sellson to achieve
f lv control successfullv (Mourier , 1972). Inundatiq releases of
S. endius against house fly cowlations i n coulttv fann, comcvrrcial - - dairy, feeding station of a Dasture land and a beef farm in Florida
have yielded an effective control of M . danestica (Mrqan g c., 1975). m e ima of carasitoid releases was reflected in the
i n r r c s l ~ in parmitian of field arwria and a decline in the adult
Doarlntion (Morgan, 1980). M e host-mrasitoid r e l a t i m h i ~ as wall
M #ypulatim dynmnics had been studied by augmentative releases of
S. endiuo t o summan house flv pawla t i au under field conditions - - (Noqan and Patterwn, 1976: Morgan 5 &., 1976). h-oqranned
rele8.~0s of 2. and 2. ra~tor were carried out aqainst field
oaoulations af ter estimstinq the breeding wtential of M. domestirs
ilaaatures (Norqan & g., 1981 ) .
Field inundatinq releases of P. vindmiae have achieved the
control of houae f l i e s , stable f l i e s and PRnnia am. in a multrv
houw and a box s t a l l . A m l a t i m model han also been derived to
determine the paxrlation dmmics of ~a ra s i to id in the field (Pickens
et g., 1975). Weekly inundatinq releases of g. vindmiae in a dairr - farm in Pondicherry, India t o check the f ly nuisance achieved an
increase in the natural oarasitism and a reductim in f ly q r i l l
counts (Panicker and Srinivrraan, 1986).
Pawson and Patterson (1988) have studied tho imct of E.
raleanes and its disrr?r-1 Mttern in eastern Nebraska (U.S.A.) and I
found that s ~ e c i e s was not a m r e n t and the averaqe p~ras i to id
emerqence i n each side of the release mint was not significantly
different. The influence of habitat and t m r a t u r e was studied on
d i m e r ~ a l behaviour of 13. and U. nlfices durinq inundatinq
releaees in a dairy barn a t Nev York (U.S.A. ) and an increase in
met release ~ r a s i t i s m wan &served. E. raDtor w a s found to hn
efficient both in diswr.sa1 and field oaraaitization (Smith & g.,