CARIBBEAN Vol. XX FOOD CROPS SOCIETY Sociedad Caribefia de Cultivos Alimenticios Association Caraibe des Plantes Alimentaires

PROCEEDINGS OF THE 20th ANNUAL MEETING - ST. CROIX, U.S. VIRGIN ISLANDS - OCTOBER 21-26, 1984

^MAI t FARM

IN THE CARIBBEAN!

Published by THE EASTERN CARIBBEAN CENTER, COLLEGE OF THE VIRGIN ISLANDS and THE CARIBBEAN FOOD CROPS SOCIETY Recent Advances in Research on Control and Biology of Pickleworm and Melonworm Kent Elsey, Jorge Pena, Joop Peterson, Todd Wehner

USDA, ARS, in cooperation with other institutions, has tion stimulancs, foreign exploration and importation of been conducting research on pickleworm and melonworm parasites from South America and the Caribbean, and popula- ( spp.: Pyralidae) for several years. Recent advances tion dynamics of Diaphania spp. in tropical Florida. in this research are given. Topics discussed include: research Keywords: Diaphania nitidalis, Diaphania hyalinata, Cucur- on plant resistance in and squash, role of oviposi- bita, Cucumis.

A mainstay of small farm opetations is vegetable production, Another series of antibiosis tests run on a number of cultivated with cucurbit vegetables, such as cucumber and squash, being an species of cucurbits found that only Lagenaria siceraria, an inedi- important parr of vegetable farming. For example: in Notth ble species of goutd, demonstrated a significant degree of Carolina almost 40,000 acres of are grown, mostly on tesistance (Elsey, 1981). This and the cucumber work indicates small farms. In the southeastern U.S. the key insecr pest of cucur- that antibiosis among cucurbit vegetables may not be a useful bits is the pickleworm, Diaphania nitidalis Stoll. The picklewotm factor in breeding for pickleworm tesistance. causes primary injury by burrowing into fruit and rendeting them Studies of oviposition nonpteference have focused on dif- unfit for matket. Since shippers and packers, particularly pickle ferences between glabrous and pubescent cucumbers, com- processors, cannot tolerate infested ot damaged fruit reaching the parisons of pickleworm resistant and susceptible squash species, consumer, the economic threshold fot the picklewotm is vety low. and a study of the chemical factors involved. Thus, when picklewotm are present frequent applications of in- Foliage of cucumber and muskmelon is normally pubescent secticide are necessary ro conttol the pest. The picklewotm but glabtous mutants have been described (Foster, 1963; Robin- undergoes an annual expansion and contraction of its range in son and Mischanec, 1964). Pulliam (1979) reported that glabrous the eastern U.S. Populations move slowly north in spring and cucumbet plants seemed to be nonpreferred for pickleworm summer and then retreat south during autumn and winter as oviposition. Follow-up work by Elsey and Wann (1982), using ar- freezing temperatures kill pickleworms and available host plants. tificial infestations of moths and following natutal populations in Eventually midwinter populations are restricted to southern the field, found that both picklewotm and melonworm pteferred Florida (Dupree et al., 1955). A closely relared species, the to oviposit on the pubescent plant type (Tables 2 & 3). Unfortu- melonworm, Diaphania hyalinata L., has similar biology, except nately, the glabrous cucumber is less vigorous than the pubescent that it is strictly a defoliator. Ir can build up to economic levels in type, which may limit its use by plant breeders. mote southern areas in the U.S., such as Florida and South Carolina. Both species are present in northern South America and Several studies on pickleworm tesistance in squash have found Caribbean islands. that some moschata Poir cultivars have lowet infesta- tions of pickleworm than more susceptible species (Brett et al, The United States Vegerable Laboratory in Charleston, S.C., 1961; Dilbeck and Canetday, 1968; Dilbeck et al., 1974), but the has taken the lead in coordinating research on biology and alter- mechanism for this tesistance was not known. In rhe summer of native control measures fot these pests. In this paper we will sum- 1984 we have compared egg and larval infestations on two C. marize our ptogtess in selecred aspects of this wotk. moschata cltivats, Butternut and Calabaza wirh a susceprible L. cultivar, Tablequeen. During the peak Plant Resistance Studies oviposition period ca. 10 times as many Diaphania spp. eggs were Most of out work on plant resistance of cucurbits to picklewotm found on Tablequeen and subsequently higher numbers of both and melonworm ar Charleston and cooperating institutions has picklewotm and melonworm larvae (Table 4). Laboratory tests, to involved the roles and relative importance of antibiosis and date, have failed to detect any larval antibiosis or preference fac- oviposition nonpreference as resistance mechanisms. tors among the three cultivars, so we we feel thar oviposition non- In order to facilitate resting fot antibiosis to pickleworm among pteference is the most important resistant mechanism in the C. over 1,000cucumber cultivars and breeding lines, we developed a moschata cultivars. simple laboratory method using detached leaves. In essence, the tests involved placing newly-hatched larvae on leaves and enclos- It is probable that chemical differences among these three ing them in plastic petri plates fot several days. The plates were cultivars are responsible for the observed oviposition non- then opened to count the larvae and score rhe leaves fot damage pteference. Thus, we have been looking closely at the chemical using a scale of 1 (little damage) ro 9 (very heavy damage). Tbe influences on picklewotm oviposition using a yellow squash varie- exact methods differed slightly depending on whethet the test ty in the species C. pepo. We have found that ethanol extracts of was a preliminary screening of all lines ot later rests of the most foliage from which the volatile components have been removed resistant and most susceprible. Of the 1,160 lines tested in the in- contain chemicals that stimulate oviposition when sprayed on a itial screening test, 8 were selecred for further studies (5 resistant suitable medium (pads of fiberglass insulation). We have further and 2 susceptible). These lines and their performance are shown found that pumping air containing squash volaciles into pads in Table 1. The range of scores from most resistant to most sprayed with exttact incteases oviposition over pads with extract susceprible was narrow, ranging from 3.0 ro 6.5, or 3.1 to 4.5 only. From these and other experiments we can outline the depending on the tesr. In a further study, a patent-progeny following hypothesized mode of action (Fig. 1). regression analysis run on a population developed from the resis- We are now in the process of testing the model and rrying ro tant lines revealed a heritability of neatly 0 (Wehnet et al., 1983). identify the volatile and nonvolatile chemicals involved.

100 PROCEEDINGS ol the CARIBBEAN FOOD CROPS SOCIETY-VOL. XX FIGURE 1. TABLE 2. Ovipniuon by Dvpbtma moths on glabrous and pubescent cucumber in Kieenhoiue.

PLANT VOLAT1LES X_egge/glant Planttjge SEARCHING + Pickleworm Melonwora GRAVID PHYSICAL ATTRACTION FEMALE FACTORS Glabrous 18.5a 15.9a (color, outline, etc.) Pubescent 114.2b 47.1b NONVOLATILE CHEMICAL FACTORS

PHYSICAL FACTORS (pubescence, etc.) Preliminary surveys found the Melothria pendula L., creeping I Momordicachorantia cucumber, and L., wild balsam apple, were abundant throughout Florida, therefore our field and laboratory ARREST, work to assess the importance of wild hosts was concenttared on oviposmoN STIMULATION, these rwo species. From November 1983 through April 1984 at INDUCTION three locations in southern Florida, 79 pickleworms were found on Melotbria and 0 on Momordica while 8 melonworms were found on both species. Survival of newly hatched melonworm and pickleworm on Melotbria foliage was equal ro that of the cucumber check, but development was somewhat delayed. Sur- vival on Momordica was 0 for both species. No feeding was Biology in Southern Florida observed and the larvae wandered rhe leaves until they eventually Momordica Laboracory tests at Charleston have demonstrated, at least starved to death. The lack of pickleworm on in the theoretically, the potential of controlling pickle worm by release field can be explained by their failure ro feed on excised foliage, of irradiated substerile male moths (Elsey and Brower, 1983). The bur since melonworms also did not survive, rheir presence in field constriction of the overwinrering range of melonworm and sample is puzzling. We arc investigating the possibility of a Momordica. pickleworm to southern Florida presenrs the limited geographical melonworm race adapted to feeding on The presence Melotbria range that is a prerequisite of the sterile male technique. of both species in field samples of , their ability to feed However, before this or any other region-wide control technique and develop on the weed, and its abundance throughout Melotbria is implemented, a thorough study of the species biology in its southern Florida indicate that is a very important alter- overwintering refuge is necessary. Therefore, in early 1983 the nate host. USDA and University of Florida initiared a cooperative study of pickleworm and melonworm biology in southern Florida. The Biological Control objectives of the study were to determine the seasonal fluctuations The impact of natural enemies on pickleworm and melonworm in density of the two species on trap crops of cucumber and squash, in the U.S. decreases in a northernly direcrion. In a two year commercial cucurbit fields, and stands of potenrial weed hosts at study in North Carolina (Van Balen, 1976) no parasires were several locations. Additional information was to be gathered on in- found on pickleworm. In the Charleston, S.C. area an uniden- cidence of parasitism. Much of this work is still in progress and i t is tified species of Apanteles attacks both species consistently late in too early for a comprehensive report; however, interesring informa- the season and egg parasirism by Tricbogramma can be high tion on the importance of wild hosts is already available. (Elsey, 1980). Nothing was known concerning parasitism in southern Florida prior to the start of our biology study there, but we suspected there would be more parasite species involved. Dr. Jorge Pena has found rhe following species of hymenopterous parasites in southern Florida during the last 18 months. Apanteles sp. Braconidae TABLE 1. Performance of eight selected cucumber lines in two antibiosis tests. Hypomtcrogaster sp. Braconidae Gambus ultimas Ichneumonidae Cultlva r Detached-lea f *Pristomerus spinator Ichneumonidae 2 OI Test Score Temelucba sp. Ichneumonidae Hank Lin e Teat 1 Tes t 2 Ictoplectis inquisitor Ichneumonidae *Casinaria infesta Ichneumonidae 1 C541 CZ 3. 0 3. 1 Spilochalcts sp. Chalcididae 2 Pemscore 3. 0 3. 2 Cerapbron sp. Ceraphronidae

3 PI 20599 6 3. 0 3. 2

4 RS 7903 1 3. 0 3. 3 TABLE 3. Mean number Dupbtnia spp. eggs (pickleworm and melonworm) on 5 Earllpl k 1 4 3. 5 1. 5 gbbcous and pubescent cucumber plant.

1158 HSU 58 1 H 5. 5 5. 0 Diaphani a spp . eggs/plan t 1159 PI 26307 9 6. 5 4. 3 Glabrous Pubescen t 1160 VD? No. 32 8 6. 5 4. 5 8/1 9 . 5 6. 0

8/2 6 1. 2 z 31. 2 lea f damage aeore d 1 t o 9 <1 - n o damage, 9 » lea f tlaeu e betvee n vein s completel y eaten) . 9/ 3 . 2 2. 3

100 PROCEEDINGS ol the CARIBBEAN FOOD CROPSSOCIETY-VOL .XX Dr. Pena has also collected in his native country. Colombia, and On St. Croix, Knausenberger and Bland have found two new found: species of Ichneumonid parasitizing melonworm, the most Poly cry tus sp. Ichneumonidae important being Agrypon caribbaeum (Bland, 1984). I have *Cardiocbiles new sp. Bracon id ae found in laboratory tests that rhis species also successfully Hypomicrogaster sp. Braconidae parasitizes the pickleworm. 1 found in Puerto Rico a uniparental Brachmeria sp. Chalcidae species of Ttichogramma that is currently under culture at *Spilochalcis sp. Chalcidae Be ltsville, MD. Ftom rhis limited amount of work, it would seem •Under culture at Homestead. FL. there is great potential for finding effecrive parasites in northern South America and the Caribbean basin for release in Florida for mote effective natural conrrol of pickleworm and melonworm in TABLE 4. Field infestation of pickleworm and melonworm on squash culcivars the U.S. Tablequeen, Butternut, and Calabaza.

X ]>irvae/i>)antb

X ew.s/plortr1 Melonvorm p i c k1eworm '1 .lb 1 tM|uecn 4 a AO.1 a 4.9a (C. pc[v>) TABLE 5. Suninl and ficsi stage duration of (lest instar piddewoim -and melon- Kultcrmil i.l 1> 3,2 I) .1 l> worm larvae. (C. mr>He!i."il*0 4.0 i> b .? h (C. mosi'li-it-'l) % survival Days to first molt fln&t Pickleworm Kelonworm Plckleworra Melonworm Cucumber 84.0a 'iU. 0a 2.1a 2.2a 3.7b 2.8b vi x <>r roiincs nn 8/1 and 8/8 Melothrin 78.0a 90.0a i) x or conn I s on H/fl .-ind Homordica flb 0b T

References 8. Elsey, K.D., and E.V. Wann 1982. Differences in iufestation of pubescent and glabrous forms of cucumber by pickleworms and melonworms Hon. Science I Bland, R.G. 1984. Agrypon caribbaeum, a new species of Ichneumon Wasp 17:253-254. (Hymenoptera:Ichneumonidae) From ihe U.S. Virgin Islands. Ann. Emomol. Soc. 9. Elsey, K.D., and J.H, Brower. 1985. Sterilization of pickleworm by ionizing Am. 77-29-31. radiation or heat. j. Econ. Entomol. In press. 2. Bmi, C.H.. C-l. Combs, and D M. Daugherty.1961. Resistance of squash 10. Foster, R.E. 1963. Glabrous, a new seedling marker in muskmeJon. J. varieties u» the pickleworm and the value of lesisiaiKe 10 insetikridal control. J. Hered. 54:113-115. Eton. Emomol. 54:1191-1197. 11. Pulliam, T.L. 1979. The effect of plant types and morphology of the 3- Dilbeck, J.D., and T.D. Canerday. 1968. Resistance of Cucurbita to the cucumber, Cucumts sativus L., on infestation hy the pickleworm, Diaphania pkklcworm. J. Econ. Emomol. 61:1410-1413. miidaiis (Stoll). M.S. Thesis, Department of Horticulture, NC State University. 4. Dilbetk J.D.J. W.Todd, and T.D. Canerday. 1974. Pickleworm lesistance 12. Robinson, R.W. and W. Mischanec. 1964. A radiation induced seedling in Cucurbita. Fla. Emomol. 17:27-37. marker gene for cucumbers. Veg. Improv. News!. 6:2. '). Duprct, M.. T L. Bissell. and C.H. Beckham. 1935. The pickleworm and its 13. Van Balen, L. 1976. The biology of the pickleworm {Diaphania nittdahs control. Ga. Agric. Exp, Sia. Bull. N.S. 5:34 pp. [Scull], :Pyralidac) in North Carolina, M.S. Thesis. Department of En- 6. Elsey, K.D. 1980. Pickleworm: MoriaJiiy on tucumbers in the field. En- tomology, NC State University. viron. limumol, 9:806-809. 14. Wehner, Todd C.. George G. Kennedy, and Kenl D. Elsey. 1983. 7. Elsey, K.D. 1981. Picklcworm: Survival, development, and oviposiiion on Resistance of Cucumber to the Pickleworm. 1983 Cucurbit Genetics Coopeiative selecitd hosis. Ann. Emomol. Soc. Am. 74:96-99. Report.

102 PROCEEDINGS Ol tha CARIBBEAN FOOD CROPS SOCIETY—VOL. XX