Periodic collections of the bird cherry-oat aphid, Rhopalosiphum padi, during two years revealed small populations on winter wheat in Lafayette, Indiana. The greatest numbers were found on volunteer wheat plants before planting. In the autumn, aphids were detected on one-shoot plants by mid-October and also early March. The populations remained small until mid-June. We conclude that the aphid feeding did not significantly affect the plants, but helped spread barley yellow dwarf virus

Araya, J. E

Cambron, S. E

Foster, J. E

English

Valparaiso University

The Great Lakes Entomologist Volume 20 Number 1 - Spring 1987 Number 1 - Spring 1987 Article 5 April 1987 A Study of the Biology of Rhopalosiphum Padi (Homoptera: Aphididae) in Winter Wheat in Northwestern Indiana J. E. Araya University de Chile J. E. Foster Purdue University S. E. Cambron Purdue University Follow this and additional works at: https://scholar.valpo.edu/tgle  Part of the Entomology Commons Recommended Citation Araya, J. E.; Foster, J. E.; and Cambron, S. E. 1987. "A Study of the Biology of Rhopalosiphum Padi (Homoptera: Aphididae) in Winter Wheat in Northwestern Indiana," The Great Lakes Entomologist, vol 20 (1) Available at: https://scholar.valpo.edu/tgle/vol20/iss1/5 This Peer-Review Article is brought to you for free and open access by the Department of Biology at ValpoScholar. It has been accepted for inclusion in The Great Lakes Entomologist by an authorized administrator of ValpoScholar. For more information, please contact a ValpoScholar staff member at scholar@valpo.edu. 1987 THE GREAT LAKES ENTOMOLOGIST 47 A STUDY OF THE BIOLOGY OF RHOPALOSIPHUM PADI (HOMOPTERA: APHIDIDAE) IN WINTER WHEAT IN NORTHWESTERN INDIANA1 J. E. Araya2 , J, E. Foster3 , and S. E. Cambron 3 ABSTRACT Periodic collections of the bird cherry-oat aphid, Rhopalos phum padi, during two years revealed small populations on winter wheat in Lafayette, fudiana. The greatest numbers were found on volunteer wheat plants before planting. In the autumn, aphids were detected on one-shoot plants by mid-October and also early March. The populations remained small until mid-June. We conclude that the aphid feeding did not significantly affect the plants, but helped spread barley yellow dwarf virus. The bird cherry-oat aphid, Rhopalosiphum padi (L)., is an important insect pest ofcereals, damaging the hosts both y feeding and by transmitting barley yellow dwarf virus (BYDV) (Stem 1967, Kolbe 1973). In the United States, severe epidemics of BYDV in small grains apparently occurred prior to 1951 (Anon. 1959, Bruehl 1961 , Rochow 1961). The aphid has a wide range of hosts that include various species of eereals and grasses as sununer hosts, and Prunus spp. as fall and spring hosts (Richards 1960, Robinson and Hsu 1963). Several reports documented losses in small grains due to feeding damage, BYDV, and their combined action. For example, in Indiana yield losses were estimated at about 27.5% in oats due to infection by BYDV in 1959 (Caldwell et al. 1959), while in Mississippi, reported losses in oat yields were as high as 30-40% (Rothman et al. 1959). In Canada, seed weight losses f 60-86% occurred for spring wheats naturally infected with BYDV in 1978 (Gill 1980). Fall infections of BYDV on hard red winter wheat in Kansas caused yield reductions of 25-60%, while spring infection yield reductions were 5-35% (Palmer and Sill 1966). Similar results were obtained by Carrigan et al. (1981). In Italy, spring barley, immediately after sprouting became infested by aphids that had previously developed on maize (Suss and Colombo 1982). In the autumn, aphids (especially R. padi and Sitobion avenae (Fabricius» infested the basal leaf-sheaths of maize, from which they migrated to the tender shoots of well-fertilized wheat and barley when the maize plants dried up. A relationship was established between spring cereals and R. padi and Metopolophium dirhodum (Walker), which were able to transmit BYDV from maize (on which it produced no symptoms) or wild grasses and pass it on to wheat and barley. The interaction of R. padi with cereals warrants the study of its biology and makes the study of its relationships with BYDV a neccssity. The objectives of this research were to IBased on a portion of the research of the senior author in partial fulfillment of the Ph.D. degree, Purdue University. Journal Paper No. 10,830, Purdue University Agricultural Expelimenl Station. 2Depto. Sanidad Vegetal, Facultad de Ciencias Agrarias y Foreslales, Univ. de Chile. Casilla 1004-Santiago, Chile. 3USDA-ARS, Department of Entomology, Purdue University, W. Lafayette, IN 47907. 1Araya et al.: A Study of the Biology of <i>Rhopalosiphum Padi</i> (Homoptera: APublished by ValpoScholar, 198748 THE GREAT LAKES ENTOMOLOGIST Vol. 20, No. I study the life cycle of R. padi on winter wheat in the field, in order to evaluate the feasibility of controlling alate migrant aphids (BYDV vectors) in early fall, and late spring crops. MATERIALS AND METHODS The number of R. padi on wheat was determined from weekly samples of 50 stems. These were taken randomly from four blocks with three wheat plots each, corresponding to three differ nt wheat rotations with com and soybeans from the USDA-ARS Integrated Pest Management Project at the Purdue University Agronomy Faml located near Lafayette, Indiana. Samples were taken throughout the year when the crop was present for two years, starting in September 1982 with volunteer wheat plants. Winter wheat seedlings were sampled during the fall of 1982, and in the same fields during spring 1983. The second season commenced October 1983 and continued through June 1984 except in midwinter. Since many R. padi develop within the seedling leaf whorls, the sample plants were cut at ground level and placed in vials in 70% alcohoL The aphids per seedling or per stem in taller plants, were counted later in the laboratory. This method has proven to be effective in determining the proportions of different morphs of S. avenae in field studies in England by Dewar et al. (1982). RESULTS AND DISCUSSION The numbers of R. padi collected periodically on winter wheat plots during two crop cycles (1982-83 and 1983-84) appear in Figure 1. The data are expressed as the average number of nymphs, apterae, and alatae collected on 50 stems. The wheat plots where the aphids were collected were part of a study with three different rotations including wheat, com, and soybeans, the most common crops in Indiana. The aphids collected are representing the average number occurring in winter wheat rotated with other crops. Aphid numbers were low during both crop years. The highest populations occurred in 1982 on volunteer wheat plants just prior to fall planting (Fig. I). These and other graminaceous plants were important sources of aphid infestation and BYDV inoculum for wheat seedlings in October. The small seedlings are often invaded by alate aphids that are efficient vectors of the virus (Gill 1970, 1972). Even though present in small numbers, they spread the virus in the crop when it is most susceptible (Endo and Brown 1963, Smith 1961). It has been reported that a fall infection of winter wheat by BYDV is more severe than a spring infection (Palmer and Sill 1966). During a mild winter, some aphids may survive, and although normally inactive during the cold months (Forbes 1962, Harper and Blakeley 1968), they become active and start reproducing parthenogenetically earlier in spring (Dixon 1971), causing larger infestations than average. In 1983, the nrst aphid nymphs were collected on 5 March, when the plants were in the one-leaf stage (stage 1 of the Feekes scale [Large 19541) and probably were progeny f winged immigrants that had arrived earlier. The nrst winged individuals were collected on 20 May. The populations were relatively small until mid-June, when aphids were easily detected by sight; however, by this time the crop had flowered (stage 10.5.4 of Feekes) and most of the aphids were below the heads. It is thought that plants can withstand such infestations without any adverse effect on the yield. As the crop matured and the temperatures of summer increased, the populations declined to nearly negligible levels. The heat and drought of the summer of 1983 are believed to have been the cause of the small population available to attack wheat the following fall. The aphids were detected on 14 October 1983, on plants at the one-leaf stage, and winged immigrants were collected on 26 October. The population remained small until 8 June and reached a peak on 15 June. This increase occurred after all the heads had formed and were out of the sheath 2The Great Lakes Entomologist, Vol. 20, No. 1 [1987], Art. 5https://scholar.valpo.edu/tgle/vol20/iss1/51987 THE GREAT LAKES ENTOMOLOGIST 49 (/) ::::t 4Q~ W L ~ 20j ~ 0 '"-=S:C:E:C-pT-'-O-C-T-r-N-O-Y""(/) MAR APR MA Y JUNE OCT 'NOY MAY JUNE 1982 1983 19849 ::r: Q. « LL o a: W CD ::::t 10 ::) Z o 10.5.2 10.1 11.1 , I j , SEPT ' OCT' NOY MAR ' APR MAY , JUNE ' 'OCT 'NOY' 1982 ALATAE 1983 Figure 1. Numbers of Rhopa/osiphum padi collected on wheat plots in the Integrated Pest management Area at the Purdue Agronomy Farm (stage 10.5 of Fe ekes); the maximum number occurred during the ripening (stage 11), and was of a relatively low level. We conclude that in 1984 the crop was unaffected by direct aphid feeding. From this study, aphids invaded winter wheat crops in the area of Lafayette, Indiana, early in the season, enabling winged immigrants to spread BYDV when the crop was most suseeptible to the virus. Relatively large numbers of winged aphids sueh as found on volunteer wheat in September of 1982, pose a danger to wheat crops in Indiana that may 3Araya et al.: A Study of the Biology of <i>Rhopalosiphum Padi</i> (Homoptera: APublished by ValpoScholar, 198750 THE GREAT LAKES ENTOMOLOGIST Vol. 20, No. I become infected very early with BYDV. This danger may increase as minimum tillage practices gain widespread acceptance, leading to more volunteer wheat. LITERATURE CITED Anonymous. 1959. The epidemic of barley yellow dwarf f oals in 1959. Plant Dis. Rep. Suppl. 262:316-384. Bruehl, G. W. 1961. Barley yellow dwarf, a virus disease of cereals and grasses. Monograph No. I, Amer. Phytopath. Soc. 52 pp. Caldwell, R. M., J. F. Schafer, L. E. Complon, and F. L. Patterson. 1959. Yellow dwarf infection on oals and wheat in Indiana in 1959. Plant Dis. Rep. Supp!. 262:333. Carrigan, L. L., H. W. Ohm, J. E. FOSler, and F. L. Patterson. 1981. Response of willier wheat cultivars to barley ycllow dwarf virus infection. Crop Sci. 21 :377-380. Dewar, A. M., G. J. Dean, and R. Cannon. 1982. Assessmenl of methods for estimatillg the numbers of aphids (Hemiptera: Aphididae) in cereals. Bul!. Entomo!' Res. 72:675-685. Dixon, A. F. G. 197 L The life-cycle and the host preference of the bird cherry-oat aphid, Rhopalosiphum padi L., and their bearing on the theories of host altemation in aphids. Ann. App!. Bio!. 68: 135-147. Endo, R. M., and C. M. Brown. 1963. Effects of barley yellow dwarf virus on yield f oats as influenced by variety, virus strain, and developmental stage of plants at inoculation. Phytopathology 53:965-968. Forbes, A. R. 1962. Aphid populations and their damage to oats in British Columbia. Canadian 1. Plant Sci. 42:660-666. Gill, C. C. 1970. Aphid nymphs transmit an isolate of barley yellow dwarf virus more efficiently than do adults. Phytopathology 60:1747-1752. 1972. Further studies on the transmission of certain isolates of barley yellow dwarf virus by nymphs and adults of Rhopalosiphum maidis. Canadian J. Plant Sci. 52:107-109. ___. 1980. Assessment of losses on spring wheat naturally infected with barley yellow dwarf virus. Plant Disease 64:197-203. Harper, A. M., and P. E. Blakeley. 1968. Survival of Rhopalosiphum padi in stored grain during cold weather. J. Beon. Entomo!' 61:1455. Kolbe, W. 1973. Studies on the occurrence of cereal aphids and the effect of feeding damage on yields in relation to infestation density levels and control. PfIanzenschutz Nachrichten Bayer 26:396-410. Large, E. C. 1954. Growth stages in cereals. Illustration of the Feekes scale. Plant PathoL 3:128-129. Palmer, L. T., and W, H. Sill, Jr. 1966. Effect of BYDV on wheat in Kansas. Plant Dis. Rep. 50:234-238. Richards, W. R. 1960. A synopsis of the genus Rhopalosiphum in Canada (Homoptera: Aphididae). Canadian Entomo!. 92 (Supp!. 13):5-51. Robinson, A. G., and S. Hsu. 1963. Host plant records and biology of aphids on cereal grains and grasses in Manitoba (Homoptera: Aphididae). Canadian Entomo!. 95:134-137. Rochow, W. F. 1961. The barley yellow dwarf disease ohmall grains. Adv. in Agron. 13:217-248. Rothman, P. G., D. H. Bowman, and S. S. Ivanoff. 1959. Occurrence of barley yellow dwarf on oats in Mississippi, 1959. Plant Dis. Rep. Supp!. 262:348-350. Smith, H. C. 1967. The effects of aphid numbers and stage of plant growth in delermining tolerance to barley yellow dwarf virus in cereals. New Zealand 1. Agric. Res. 10:445-466. Stem, V. M. 1967. Control of the aphids attacking barley and analysis of yield increases ill the Imperial Valley, California. J. Econ. Entomo!. 60:485-490. Suss, L., and M. Colombo. 1982. [Cereal aphids.] Gli afidi dci cereali. Informatore Fitopatologico 32:7-12. 4The Great Lakes Entomologist, Vol. 20, No. 1 [1987], Art. 5https://scholar.valpo.edu/tgle/vol20/iss1/5

A Study of the Biology of \u3ci\u3eRhopalosiphum Padi\u3c/i\u3e (Homoptera: Aphididae) in Winter Wheat in  Northwestern Indiana

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A Study of the Biology of \u3ci\u3eRhopalosiphum Padi\u3c/i\u3e (Homoptera: Aphididae) in Winter Wheat in Northwestern Indiana

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