1 Suction Trapping of Selected Small Grain Aphids in Colorado, 1988-1998 Robert W. Hammon1, Terri L. Randolph2, J. Scott Armstro
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Suction Trapping of Selected Small Grain Aphids in Colorado, 1988-1998 Robert W. Hammon1, Terri L. Randolph2, J. Scott Armstrong3, Cynthia B. Walker4, Jeffrey B. Rudolph2, Michael D. Koch5, Wendy L. Meyer6, and Frank B. Peairs2 1 Fruita Research Center, 1910 L Rd., Fruita, CO 81521 2 Bioagricultural Sciences and Pest Management, Colorado State University, Fort Collins CO 80523 3Plant and Soil Science, Texas Tech University, Lubbock TX 79409 4Colorado State University, 1001 S. Main, Lamar CO 81052 5 USDA Central Great Plains Research Station, P.O. Box 400, Akron CO 80720 6TREC, 18905 SW 280th St., Homestead FL 33031 1 Aphids are serious pests of small grains climactic conditions. Eggs are much less worldwide because of direct feeding damage and vulnerable to climactic extremes than living the ability to transmit plant pathogens. In aphids, so Russian wheat aphid populations are Colorado, the major cereal aphid pests are the more stable from year to year in areas where Russian wheat aphid, Diuraphis noxia there is no sexual reproduction. Males have never (Mordvilko), greenbug, Schizaphis graminum been found in North America so all reproduction (Rodani), and bird-cherry oat aphid, is assumed to be asexual. Russian wheat aphids Rhopalosiphum padi (L.). The Russian wheat spend the winter as living aphids, feeding on host aphid, introduced into the United States in 1986, plants when climactic conditions permit causes chlorotic leaf streaking, leaf stunting and (Hammon and Peairs, 1992). When winters are rolling, and trapped and distorted heads. Losses very cold or there is extended snow cover, to Russian wheat aphid have exceeded $112 Russian wheat aphid populations decrease or million in damage in Colorado (F.B. Peairs, winter kill (Armstrong and Peairs 1996, Butts unpublished) and $500 million in the USA since and Schaalje 1997). Winter mortality can occur its introduction (Morrison and Peairs, 1998). The over a large region or only within isolated greenbug and bird cherry-oat aphid cause portions of an area. When winter mortality of considerable direct damage to plant growth and aphids occurs over a large area, the region can be yield in both winter wheat and barley (Kieckhefer reinfested by flights of alatae (winged aphids) & Kantack, 1988, Ortman and Painter 1960, from another area. Russian wheat aphid Mallott and Davy 1978) and spring wheat and populations increase in the spring as they barley (Kieckhefer & Kantack 1980, Voss et. al. reproduce on wheat and barley. Local movement 1997). They are also vectors of barley yellow occurs as these aphids move within and between dwarf virus (Gildow 1984, Blackman et al. fields. This is evident in areas where spring 1987), which also causes significant damage to grains are produced, as these fields may be the world’s small grain crops (Burnett 1990). infested by alatae soon after plants emerge. As The three aphid species discussed in this the grain crop matures, many alatae are produced publication have different life histories which which migrate to oversummering host plants. Fall explain, in part, the varying patterns of suction migration occurs as aphids migrate from trap captures. oversummering host plants into the newly Russian wheat aphids feed only on emerged fall planted small grain crop. grasses, with cool season grasses that are Bird cherry-oat aphids have a variety of botanically related to wheat being preferred hosts life cycle phenotypes. Some have an obligate (Hammon et. al.1997, Kindler and Springer heteroecious (host-alternating) holocyclic (with a 1989). In eastern Europe and Asia, Russian sexual stage) life history, while others are mostly wheat aphids reproduce asexually during the holocyclic with a residual anholocyclic (asexual) spring and summer, followed by a sexual population. Some clones are permanently generation in the fall. They overwinter either as anholocyclic. In the heteroecious forms, alate eggs or living aphids, depending on local aphids migrate to chokecherry plants in the fall, 2 where overwintering eggs are produced. Eggs are capture alate aphids (Allison and Pike, 1988) laid after mating of the oviparae (egg producing which are weak flying insects responsible for females) with migrant males. Eggs are more dispersal. Alatae are formed in response to resistant to cold and dessication than living various factors, such as overcrowding and aphids. The eggs hatch in the spring. These decline in host plant suitability. The number of aphids reproduce asexually, and after one or alatae present is determined by the total number more generations on chokecherry, alatae are of aphids, growth stage of host plants, season, produced that migrate to wheat or other grasses, and other factors. Some species, such as bird where many generations of both alatae and cherry-oat aphid produce many alatae to move to apterae (wingless aphids) are produced during overwintering hosts, resulting in late season the summer. In the late summer, many bird peaks in aphid captures. Other species, such as cherry-oat aphids infest corn and other grassy Russian wheat aphid, always have a few alatae hosts, where they sometimes become abundant. present with the proportion of the population in Anholocyclic populations of bird cherry-oat the alate form increasing in response to aphids on wheat may survive the winter, feeding environmental stresses and crop maturity. near the base of plants and reproducing asexually In Europe, suction traps are used to if environmental conditions are not too severe. monitor movement of many aphid species, and to Greenbug also has a holocyclic life predict outbreaks resulting from immigrating history in parts of their range, but sexual forms aphids (Turl 1980, Dewar et al 1984). In South are rare in Colorado. The life history of Dakota, Kieckhefer et al. (1974) used suction holocyclic greenbug populations differ from that trap data to show aphid immigration was of bird cherry-oat aphid in that the egg stage is associated with low-level jet winds. Loxdale et al. spent on the same grass species that the asexual (1993) reviewed the evidence concerning short summer and fall generations feed on (monoecious and long-range movement of aphids, and holocyclic). Their life history is similar to that of concluded that while long-range movement of Russian wheat aphid in that only grasses are used aphids (>100 km) certainly occurs, it is as host plants. The host range of greenbug is infrequent. Short-range dispersal (<20 km) is different than that of Russian wheat aphid, as it much more important in the population dynamics is a serious pest of warm season grasses such as of aphid outbreaks. Halbert et al. (1998) corn, sorghum and millet in addition to wheat. presented evidence that suction trap captures Greenbugs may survive the winter by feeding on reflect aphid flight activity within a 30 km radius host plants and reproducing asexually if of the trap. Halbert and Voegtlin (1994) used the environmental conditions are not too severe. capture of host specific aphids to predict the Monitoring of aphid populations is presence of purple loosestrife, a noxious weed. important to document the extent and severity of Halbert et al. (1995) used the aphid species infestations in a particular area and aid in assemblage collected in suction traps as an predicting future infestations. Suction traps have indicator of plant biodiversity in an area. been used to monitor and forecast peak In 1983 the Western regional suction migrations of various aphids. Suction traps trapping system began to monitor barley yellow 3 dwarf virus vector activity in the Pacific Northwest (Pike et al. 1987, Allison and Pike • Akron - USDA Central Great Plains 1988, Quinn et al. 1991). This system now Research Center, 4 mi E of Akron, monitors Russian wheat aphid flight patterns to Washington Co. alert growers of Russian wheat aphid • Fort Collins - 7 mi S of Briggsdale infestations. The earliest yearly collections of (1988-1993), Weld Co.; ARDEC (1994- Russian wheat aphid have generally coincided 1998), 5 mi S of Wellington, Larimer with detectable populations in spring seeded Co. cereal crops, and have occurred before economic • Fruita - Fruita Research Center, 2 mi NE thresholds have been exceeded. Fall collections of of Fruita, Mesa Co. Russian wheat aphids have indicated that they • Walsh - Plainsman Research Center, 0.5 have successfully oversummered, and there was a mi W of Walsh, Baca Co.. potential for infestation of the fall seeded cereal • Yellow Jacket - Southwestern Colorado crop (Halbert et al. 1998). A network of suction Research Center, 1 mi N of Yellow traps was set up in small grain producing regions Jacket, Montezuma Co. of Colorado in 1988 to monitor populations of Russian wheat aphid and other small grain The traps were changed weekly at a aphids. This publication presents the results of minimum. Heavy rains, power outages and this trapping at certain locations for the period of mechanical failures have caused short term 1988-1998. It gives an important historical disruptions in data collection at all sites. Single perspective on small grain aphid abundance and missing data points were estimated by averaging movement during that time period. the two data points surrounding the missing data. If more than two consecutive weeks were METHODS AND MATERIALS missing, the points were not graphed. The data are presented in Figures 4-18 as weekly captures. Suction traps constructed to the Data points greater than zero are plotted with dot specifications of Allison and Pike (1988) were symbols. If no symbol is present, the capture was placed in the field in the spring of 1988. The either zero or missing. If there is no line traps are 28 ft tall, with an opening diameter of connecting two points, there are missing data 12 in. An electric fan pulls air through the traps points. and insects are funneled into a jar containing a Temperature and precipitation data was 50:50 mixture of ethylene glycol and 95% obtained from the Colorado Climate Center ethanol, which kills and preserves the catch.