The effect of different soybean varieties (Glycine max 356, M4, M7, M9, Clark, Sahar, JK, BP, Williams, L17, Zane, Gorgan3 and DPX) on the life history and fecundity of the gram pod borer Helicoverpa armigera (Hubner) (synonym Heliothis armigera (Hubner), also known as the American or African bollworm) was determined at 25 Ϯ 1°C, 65 Ϯ 5% r.h. and a light : dark cycle of 16:8 h. The larval period ranged 17.30 to 26.20 days on M7 and L17, respectively. The longest development time was on L17, BP and Sahar (42.71, 40.29 and 39.20 days, respectively) and the shortest was on M7, M9, Williams and Clark (34.21, 36.06, 36.60 and 36.82 days, respectively). The development index of overall immature stages varied from 1.39 to 2.41, with the minimum on L17 and BP and the maximum on M7. The highest daily fecundity and total fecundity (118.92 and 582.70 eggs, respectively) and the lowest (37.88 and 177.10 eggs, respectively) were observed on DPX and 356, respectively. Cluster analysis of the biological parameters of H. armigera on different soybean varieties demonstrated that BP, Sahar and L17 were partially resistant to H. armigera. Knowledge of the extent of susceptibility or resistance of crop varieties and biology of a pest on that crop are fundamental components of integrated pest management (IPM) programs for many crops. Such information can help to detect and monitor pest infestation, variety selection and crop breeding.

The Sunn pest, Eurygaster integriceps Puton (Heteroptera: Scutelleridae), is one of the most important pests of wheat and causes considerable damage to this valuable crop annually. Digestive proteinase activity of adult insects was investigated using general and specific substrates and inhibitors. Proteolytic activity was low when the common conventional substrates, azoalbumin, azocasein and hemoglobin were used to assay salivary glands and midguts. Using the fluorescent casein substrate (BODIPY FL casein), total proteolytic activity was measured at different pH. Maximum proteolytic activity was detected at pH 7 (100%) and 8(65%) which suggested the presence of serine proteinases in the salivary glands. There was no detectable proteolytic activity in midgut extracts. The inhibitors; PMSF (inhibitor of serine proteinases) and TPCK (a specific chymotrypsin inhibitor) showed greater than 50% inhibitory effect on total proteolytic activity, however, TLCK (specific trypsin inhibitor) and E-64(specific cysteine proteinase inhibitor) did not inhibit total proteolytic activity. Using fluorescent specific substrates for serine and cysteine proteinases (Z-Arg-AMC, Z-Arg-Arg-AMC, Z-Arg-Phe-AMC and Suc-Ala-Ala-Pro-Phe-AMZ) revealed the presence of tryptic and chymotryptic activity in the salivary gland extract. Zymogram analysis under non-reducing SDS-PAGE conditions and using the substrate APNE showed at least 8 tryptic and chymotryptic activity bands in salivary gland extracts. A single high molecular weight band with tryptic activity (165 kDa) was detected using the substrate BApNA in a zymogram analysis uisng native-PAGE. Kinetic studies showed a km value of 0.6 mM for this enzyme against the substrate BApNA .The inhibitor TLCK decreased activity of the trypsin-like enzyme up to 73% and almost completely eliminated the only band related to this proteinase in the zymogram. Soybean Kunitz type trypsin inhibitor showed no effect on proteolytic activity of the trypsin-like serine proteinase. In general, the results revealed the presence of chymotrypsin- and trypsin-like serine proteinases in the salivary gland of E. integriceps, and it seems that the major total proteolytic activity is due to chymotrypsin proteinases.

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The findings demonstrated that the cultivars L17 and Sahar were partially resistant to this pest, probably because of some secondary chemicals or proteinaceous protease inhibitors of these cultivars.

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