A greenhouse study was conducted to determine the influence of soybean cyst nematode (SCN) –susceptible and –resistant plant combinations on SCN population densities and plant growth. Purple deadnettle, annual ryegrass, SCN-resistant and -susceptible soybean were planted in pots alone or in combination at one plant pot−1. Annual ryegrass and purple deadnettle reduced soybean growth. Pots with SCN-resistant plants had lower numbers of SCN cysts and eggs than pots with SCN-susceptible plants. However, an SCN-susceptible species grown with any of the SCN-resistant plants resulted in higher cyst counts than pots with only SCN-resistant plants. From an SCN management standpoint, this research suggests that there may be no incentive to using annual ryegrass as a cover crop over planting other SCN-resistant crops to reduce SCN population density.

Weeds are alternative hosts for plant-parasitic nematodes and have long been recognized for their ability to maintain nematode populations targeted for suppression by various management strategies. The impact of weeds as alternative hosts depends largely on nematode feeding behavior, which is determined by the level of host specialization required for the parasite to feed successfully. In general, the more specialized feeding adaptations are associated with greater crop damage, more diverse nematode management options, and greater negative impact from weeds. Besides serving as alternative hosts, certain weeds can protect nematodes from pesticides and the environment, provide nematode suppression through antagonism, contribute to changes in future nematode biotic potential, or exert indirect effects through competition with crops or by the effects of weed control strategies on nematode populations. Shrinking nematicide options and increasing environmental concerns are making integrated pest management (IPM) a necessity for nematode management in many crops. A prominent similarity between most major weeds and plant-parasitic nematodes is that both are place-bound organisms that are passively dispersed. Weed–nematode interactions in agricultural production systems may be more intricate and complex than the simple function of weeds as alternative hosts. Their relationship may represent a normal adaptation resulting from the limited mobility of both groups of organisms and the obligate parasitism of phytophagous nematodes. The challenge that faces weed scientists and nematologists is to identify effective, compatible IPM strategies that address weed and nematode management collectively.

Hairy nightshade is a common weed in potato rotations in the western United States. As a close relative of potato, hairy nightshade can host numerous potato nematodes, diseases, and insect pests. Hairy nightshade hosts three common parasitic nematodes of potato, Columbia and northern root-knot nematodes, and stubby root nematode. Tubers of a potato breeding line with roots that are resistant to Columbia root-knot nematode—race 1, were damaged when grown in the presence of hairy nightshade. The weed provided an alternate host for the nematode, which then allowed the nematode to infect susceptible tubers. Stubby root nematodes transmit tobacco rattle virus (TRV), the causal agent for corky ringspot disease (CRS) of potato. CRS disease was maintained in soil when hairy nightshade was present in rotation crops of alfalfa or Scotch spearmint that otherwise eliminated the disease. Hairy nightshade also is a host of potato leaf roll virus (PLRV), which is transmitted by green peach aphids (GPA). GPA preferentially land and readily reproduce on hairy nightshade. Aphid transmission of PLRV from hairy nightshade to potato was four times greater than the virus transmission rate from potato to potato. Integrated management of these potato nematodes, diseases, and insect pests also should include strategies to control hairy nightshade in potato and rotation crops.

Soybean cyst nematode (SCN) is one of the most yield limiting pathogens in U.S. soybean production. Henbit and purple deadnettle are winter annual weeds shown to facilitate SCN reproduction after crop harvest in the eastern Corn Belt. These weeds, along with volunteer soybean that germinates in autumn after harvest, are common to postharvest soybean production fields and provide an opportunity for SCN reproduction and population increase outside of the typical soybean production season. The objective of this experiment was to determine if autumn removal of these weeds and volunteer soybean can influence the winter weed seedbank, plant biomass, and SCN population densities. Microplots were established with or without Lamium spp. and volunteer soybean, and four winter weed removal timings (none, October, December, and May). Dry weights of autumn Lamium spp. were reduced 50% in October when grown in competition with volunteer soybean. SCN juveniles were found in henbit roots at higher densities in October (42 per gram of root) than December (5 per gram of root) and were also found in the roots of volunteer soybean (14 per gram of root) in October. SCN egg population densities were 50% lower in August after the summer fallow period. The results of this experiment suggest that autumn removal of winter annual weeds and volunteer soybean did not reduce SCN populations.

The abundance and distribution of Ceratitis capitata (Wiedemann) in Late Valencia citrus orchards and other alternative host crops was investigated using trimedlure-baited traps at the University of Ghana's Agricultural Research Centre in the Eastern region of Ghana. The effect of some climatic factors on the population dynamics of the pest was also studied. The population of C. capitata increased from September to October 2006 and from February to March 2007, when Late Valencia citrus fruits were ripening or ripened. The fruit fly population was the lowest from November 2006 to January 2007 when citrus fruits were in the immature green stage. Ceratitis capitata was not trapped in mango, pawpaw and pepper fields and did not emerge from fruits of these crops. Multiple regression analyses also revealed that rainfall and temperature significantly influenced the pest population. The results of this study have important implications on the decision-making process for the safe, effective monitoring and management of C. capitata in Late Valencia citrus orchards in the study area in Ghana and probably in other areas as well.

A survey was conducted in Tororo, Bugiri and Kapchorwa districts in eastern and northeastern Uganda on farmers' perceptions of constraints in maize production. Farmers in Tororo and Bugiri consistently ranked stemborers and striga as the major production constraints in maize growing, while those in Kapchorwa ranked stemborers and lack of capital as the most important. Approximately 35 and 40% of the farmers in Tororo and Bugiri, respectively, identified stemborers as the ‘caterpillar’ that destroys their maize. In Kapchorwa, 50% of the farmers identified stemborers. Pesticide application was the most common control measure while the use of indigenous and cultural control measures was limited. Less than 50% of the farmers were aware of the existence of alternative plants/grasses on which stemborers feed. This study identified the need for creating farmers' awareness on the biology and ecology of stemborers. Empowering farmers by letting them learn and experiment will facilitate the development of innovative control measures.

The distribution and importance of stem-borer species of sorghum in Kenya, viz. Chilo partellus Swinhoe, C. orichalcociliellus Strand, Busseola fusca Fuller, Eldana saccharina Walker and Sesamia calamistis Hampson were studied and discussed. The incidence and period of activity of the stem-borer complex on sorghum indicated that C. partellus, which is a major pest, infested the crop early, while E. saccharina and S. calamistis infested late and persisted in the crop till it was harvested. Preliminary studies on the carryover of stem-borer showed that the larvae of C. partellus and S. calamistis were able to enter diapause in dry sorghum stalks for several months at the end of long and short rain seasons. Some new alternative host plants and parasites and predators affecting different life stages of stem-borers were identified. Preliminary screening of several sorghum lines was carried out for identification and confirmation of resistance to C. partellus and B. fusca, and some sources of resistance were reported.