The cowpea variety Ife BPC had yields equal to those of two other varieties tested (Ife Brown and AFB 1757) but contributed a net positive of 30.3 kg N/ha to the soil (from N contained in vegetative structures) whereas other varieties showed a net deficit. Although there was evidence that uninoculated cowpea was heavily nodulated, inoculated Ife BPC had better N content in vegetative structures (Awonaike et al., 1990).
There was a non-significant increase in cowpea grain yield up to a nitrogen application rate of 30 kg/ha (Agbenin, Lombin, and Owonubi, 1990).
Maas and Poss (1989) found used cowpea (cv 'California Blackeye No. 5') conducted pot studies in sand culture with saline solutions of various strengths (2:1 molar ratio of NaCl to CaCl) used for irrigation. Based data for the osmotic potentials that induced 50% reduction in pod and seed yields, cowpea was more susceptible to salinity increases in the vegetative (-0.45 MPA) than in the flowering (-0.76 MPa) or pod-filling (-0.88 MPa) stages. Seed number, but not individual seed size, was affected.
In Costa Rica, Bazill (1987) reported that tropical legumes showing good shade tolerance in the understory of Pinus caribaea var hondurensis were Centrosema brasilianum (L.) Benth., C. macrocarpum, C. plumieri (Pers.) Benth., and C. pubescens Benth.; Desmodium gyroides DC, D. heterocarpon (L.) DC, D. heterophyllum DC, D. intortum Mill. Urb., D. ovalifolium Wall. ex Merr, and D. uncinatumj (esp. D. heterocarpon); Flemingia congesta Roxb. Galactia striata (Jacq.) Urb., Canavaglia ensiformis (L.) DC, Lablab purpureus (L.) Sweet, and Vigna unguiculata (L. Walp.). On the other hand, performing poorly were Indigofera hirsuta L., Cajanus cajan (L.) Millsp., and Stizolobium sp. No quantitative data were given in support of these conclusions.
Maas and Poss (1989) found used cowpea (cv 'California Blackeye No. 5') conducted pot studies in sand culture with saline solutions of various strengths (2:1 molar ratio of NaCl to CaCl) used for irrigation. Based data for the osmotic potentials that induced 50% reduction in pod and seed yields, cowpea was more susceptible to salinity increases in the vegetative (-0.45 MPA) than in the flowering (-0.76 MPa) or pod-filling (-0.88 MPa) stages. Seed number, but not individual seed size, was affected.
A recommended spacing for a grain crop is 3 feet between rows, with 2-3 inches between plants, at a rate of 30-40 lb/acre (McLeod, 1982).
Seed can be drilled in rows 6-8 inches apart or broadcast at a rate of 90 lb/acre (McLeod, 1982).
The cowpea variety Ife BPC had yields equal to those of two other varieties tested ((Ife Brown and AFB 1757) but contributed a net positive of 30.3 kg N/ha to the soil (from N contained in vegetative structures) whereas other varieties showed a net deficit. Although there was evidence that uninoculated cowpea was heavily nodulated, inoculated Ife BPC had greater N content in vegetative structures (Awonaike et al., 1990).
Awonaike et al. (1990) in Nigerian field trials, determined that inoculation with any of several strains of Bradyrhizobium did not increase the biomass or N fixation by three cowpea varieties. This lack of effect was ascribed to the occurrence of the resident Bradyrhizobia bacteria in the soil.
Cowpea is a heat-adapted legume that will make maximum growth during short summer periods before late-summer or fall-planted crops (Miller, 1988). It is also suitable for summer legume cover in orchards and vineyards or undersown with corn (Peaceful Valley, 1988). To prepare poor soil before sowing a crimson clover crop, turn under two successive cowpea crops (McLeod, 1982).
Cultivars with spreading habit and luxuriant growth have been widely used as green manures. Cowpea is a promising multipurpose legume in cropping systems (Yost and Evans, 1988).
Cowpea is useful for suppressing weeds; a thick stand will smother bermudagrass (Peaceful Valley, 1988).
Cowpea can follow crops such as early sweet corn and early processing tomatoes, and precede fall-planted crops such as vegetable brassicas and cereal grains (Miller et al., 1989).
De Queiroz and Galwey (1987) tested five sorghum (S1006, 2219 B, CSH 5, CSH 6, and Ethiopian landrace E 35-1) and 2 cowpea varieties (the semi-erect C 152 and the spreading, later-maturing GFC 4) planted as sole crops and in sorghum- cowpea bicultures during the dry season. There was no significant effect of cowpea variety on sorghum yield, nor of sorghum variety on cowpea. This will probably not be the case for rainy-season plantings, in which sorghum tends to shade the intercrop more completely. For dry-season plantings, the authors suggest that a single cowpea variety might be used to evaluate sorghum performance in biculture.
At plowdown, available N from cover crops can be estimated by multiplying harvested fresh weight of cover crop from a sixteen square feet (4 x 4 ft.) sample plot by 12 (to estimate lbs of N/acre) (Miller et al. 1989).
The cowpea variety Ife BPC had yields equal to those of two other varieties tested ((Ife Brown and AFB 1757) but contributed a net positive of 30.3 kg N/ha to the soil (from N contained in vegetative structures), whereas other varieties showed a net deficit. Although there was evidence that uninoculated cowpea was heavily nodulated, inoculated Ife BPC had better N content in vegetative structures (Awonaike et al., 1990).
In southern Georgia, extrafloral nectaries of cowpea attracted 26 types of wasps, including 6 types of Vespidae, 4 Pompilidae, 10 Sphecidae, 3 Tiphiidae, and one each of Chrysididae, Scoliidae, and Ichneumonidae (Bugg, unpublished data). In California, various predatory and parasitic wasps are often seen at the nectaries, as are predatory lady beetles, Collops vittatus (striped flower beetle), various bigyed bugs (Geocoris spp.), and the pest, 11-spotted cucumber beetle (Diabrotica undecimpunctata) (Bugg, pers. comm.).
In India, Natarajan and Sheshadri (1988) assessed cotton (cv MCU 5 VT) for effect of intercropping on densities of aphid (Aphis gossypii Glover), leafhopper (Amrasca devastans Distant), bollworms (Earias insulana Boisduval and E. vittella [Fabricius]), entomophagous lady beetles (Coccinellidae) (Melanochilus sexmaculatus Fabricius and Coccinella sp.), and braconid wasps (Rogas aligarhensis Qadri and Agathis fabiae Nixon) that attack bollworms. Cotton was grown in a replicated trial under four intercropping regimes: (1) cotton and cowpea (cv Co.Vu.623); (2) cotton and soybean (cv Co.1); (3) cotton and country onion; and (4) cotton alone. The second factor was insecticidal application, assigned by a split-plot approach. No effects were observed on aphid and leafhopper populations, nor on bollworms. The latter occurred at generally low densities. Parasitism of bollworms by the braconids was higher in the cotton + soybean and the cotton + cowpea treatments. The cotton + cowpea system showed elevated densities of the coccinellids.
Red imported fire ant (Solenopsis invicta) forages for honeydew produced by cowpea aphid (Aphis craccivora) on cowpea and hairy indigo (Indigofera hirsuta) but not on sesbania (Sesbania exaltata), based on a replicated study conducted in Georgia (Kaakeh and Dutcher, 1992). Ethanol and water extractions of sesbania are toxic to S. invicta.
Rhoades (1983) found that sting nematode was moderately abundant following cover cropping with cowpea ('California Blackeye No. 5'). In two out of three years, yield of cabbage was not thereafter reduced below that obtained using the nematicide fenamiphos. Rootknot nematode, Meloidogyne incognita, failed to develop high densities on any of the cover crops, but was particularly abundant on vegetables following sesbania and cowpea.
McKenry (pers. comm.) noted that 'Blackeye 5' was resistant to Meloidogyne incognita and that 'Magnolia' was resistant to M. incognita and M. javonica.
All cultivars host Protylenchus scribneri, but this is not a problem for trees and vines (UC 4045, 1985).
In a study by Bugg and Dutcher (1989), "combine" or "reseeding" cowpea sown in early July in a mature pecan orchard (which included bahia and bermuda grasses in the understory) apparently conferred more rapid vegetational cover and better reduction of weed cover than did other warm-season legumes (lespedeza, American jointvetch, sesbania, or alyceclover). No inferential statistics on legume or weed cover were presented in this replicated study, but means were plotted through time.

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