Histological studies were conducted on cowpea pods fed upon by the coreoid pod-sucking bugs, Anoplocnemis curvipes (Fabricius), Clavigralla tomentosicollis Stå;l, C. shadabi Dolling, Riptortus dentipes (Fabricius) and Mirperus jaculus (Thunberg). Various degrees of tissue and cellular disruption were apparent, especially in the brachysclereids. They were manifested in terms of plasmolysis, cell enlargement and cell wall disintegration depending on the coreoid species involved. The feeding site and its periphery had all the cells of the brachysclereids plasmolysed, with the parenchyma having broken cell walls in the case of A. curvipes. Riptortus dentipes and M. jaculus showed similar patterns of feeding activity but less extensive levels of damage. The Clavigralla spp., however, caused cell enlargement in the brachysclereids, and broken cell walls in both the brachysclereids and the parenchyma. Damage symptoms were observed in cells far away from the feeding sites of the bugs, suggesting the possibility of sucrase activity which has been reported to cause osmotic pump feeding in the Coreidae.

The salivary glands of the cowpea pod-sucking bugs Anoplocnemis curvipes (Fabricius), Clavigralla tomentosicollis Stål, Clavigralla shadabi Dolling, Riptortus dentipes (Fabricius) and Mirperus jaculus (Thunberg) are described and illustrated. Extracts of the glands were assayed for the presence of proteinases, α-amylase, β-amylase and amyloglucosidase. The salivary glands consist of four-lobed principal glands and a tubular accessory gland, and they differ in shape and size among the different species except for the median lobe, which is more or less spherical. The sickle-shaped nature of the posterior lobe reported before for Riptortus linearis (Linnaeus) was also observed in R. dentipes, suggestive of a probable generic characteristic. Anoplocnemis curvipes has the biggest salivary gland, and it is followed by R. dentipes, M. jaculus, C. tomentosicollis and C. shadabi in descending order. Assays of the gland extracts revealed that the four digestive enzymes tested are present in the five coreoid species. Proteinases were preponderant (1.4–94.9 μg/ml), while amylases were detected in traces [(0.5–11.0) × 10− 3 μg/ml]. Proteinases may be largely responsible for the feeding damage caused by the coreoid species and their concentration in the glands of the different species correlates well with their known capacity to inflict pod damage and yield reduction in cowpea. Fourth instar nymphs of the different species also had higher concentrations of the digestive enzymes compared with their respective adults; and this correlates with the known ability of the nymphs to cause greater pod damage and yield reduction than adults.

Feeding trials were conducted on three (young, mid-fill and mature) developmental stages of cowpea Vigna unguiculata ssp. unguiculata pods in the screenhouse using fourth instar nymphs and adults of Anoplocnemis curvipes (Fabricius), Riptortus dentipes (Fabricius), Mirperus jaculus (Thunberg), Clavigralla tomentosicollis Stål and C. shadabi Dolling. Anoplocnemis curvipes was observed to be the most damaging coreoid species causing a yield reduction of 26.4–51.7% followed by R. dentipes (24.4–29.4%), M. jaculus (21.9–26.9%), C. tomentosicollis (17.9–22.4%) and C. shadabi (15.9–20.4%). The fourth instar nymphs of each pod-sucking bug species caused a significantly higher cowpea yield reduction than their respective adults. Similarly, infestation on young pods compared to mid-fill and mature stages resulted in significantly higher yield reduction. The results suggest that infestation levels of two fourth instar nymphs of A. curvipes or three fourth instar nymphs of the other four pod-sucking bug species per young pod should be adequate for screening of cowpea varieties for resistance to the coreoid bugs.