Seeds from nine kenaf genotypes (Cubano, Everglades 41, Everglades 71, GR2563, Guatemala 48, Indian, 178-18RS-10, Tainung #l, and Tainting #2) were evaluated for oil, fatty acid, phospholipid, and sterol content. Oil content ranged from 21.4 to 26.4% with a mean of 23.7%. Total phospholipids ranged from 3.9 to 10.3% of the oil, with a mean of 6.0%. Mean sterol percent was 0.9 and ranged from 0.6% of the total oil for 178-18RS-10 accession to 1.2% for Everglades 71. Palmitic (20.1% of the total fatty acids), oleic (29.2%), and linoleic (45.9%) were the major fatty acids, and palmitoleic (1.6%), linolenic (0.7%), and stearic (3.5%) were the minor components. Medium (Ci2-Ci4) and long (C22-C24) chain fatty acids were less than 1%. Sphingomyelin (4.42% of the total phospholipids), phosphatidyl ethanolamine (12.8%), phosphatidyl choline (21.9%), phosphatidyl serine (2.9%), phosphatidyl inositol (2.7%), lysophosphatidyl choline (5.3%), phosphatidyl glycerol (8.9%), phosphatidic acid (4.9%), and cardiolipin (3.6%) were identified in the nine genotypes. Phosphatidyl choline, phosphatidyl ethanolamine, and phosphatidyl glycerol were the dominant phospholipids. In addition, eight unidentified phospholipids were also found. /I-sitosterol (72.3% of the total sterols), campsterol (9.9%), and stigmasterol (6.07%) were prevalent among kenaf genotypes. Kenaf's relatively high oil content and its similarity to cottonseed oil suggest that the seed oil may be used as a source of edible oil. The variation among genotypes indicates potential for genetic improvement in oil yield and quality.

There is little information available about phytosterols in canola (Brassica napa L.) oil and the effects of genotype and growing locations from Virginia and the mid-Atlantic region of the United States, a potential area for the establishment of domestic production to provide edible oil. Our objectives were to characterize the phytosterols, phospholipids, unsaponifiable matter, and FA in oil from Virginia-grown canola. Among 11 canola genotypes grown at two locations during 1995-1996 significant variations existed for oil content and FA profiles, but not for contents of phospholipids, unsaponifiable matter, total phytosterols, campesterol, stigmasterol, and βsitosterol. Total phytosterol content in the oil of Virginia-grown canola varied from 0.7 to 0.9% with a mean of 0.8%. This concentration compared favorably with oil from Canadian canola, which typically contains 0.5 to 1.1% total phytosterols. The mean contents of brassicasterol, campesterol, stigmasterol, βsitosterol, ∆ 5 -avenasterol, and ∆ 7 -stigmastenol as percentages of total phytosterols in Virginia-grown canola were: 9.7, 32.0, 0.6, 49.3, 4.99, and 3.5%, respectively. Growing location did not affect phytosterols in Virginia-grown canola oil but had significant effects on contents of phospholipids, and saturated (myristic, stearic, and arachidic) and unsaturated (palmitoleic, linoleic, linolenic, eicosenoic, and erucic) FA.

The tropical legume sunn hemp (Crotalaria juncea L.) could be a valuable green manure/cover crop for vegetable producers in the southeastern USA because of its rapid growth and large N 2 fixing ability. Planting and termination date effects on biomass and N accumulation are relatively unknown for the region, but would help producers manage sunn hemp between summer and winter cash crops. We determined sunn hemp biomass and N content at 30, 60, 90, and 120 days after planting (DAP) for four planting dates (

Soyfoods are becoming popular among American consumers because of potential health benefits. However, specific information about the kind of soybean [Glycine max (L.) Men.] seed desirable for soyfoods preparation is limited. The objectives of this study were to compare soymilk and tofu prepared from 12 soybean genotypes grown at four locations in the southern USA during 1995 to identify genotypes suitable for soymilk and tofu manufacture and to determine effects of seed traits on yield and quality of soymilk and tofu. Location effects were significant only for soymilk solids and tofu strength. Soymilk yield with a mean value of 5.1 mL g−1 seed was not affected by soybean genotype. Significant genotypic effects were observed on tofu yield, which varied from 0.82 to 0.91 g mL−1 of soymilk. Tofu yield was significantly correlated to seed size (+0.31), seed oil (+0.74), rate of water absorption after 1 and 16 h of soaking (+0.38 and +0.56, respectively), and seed protein (−0.82). Seed protein content, seed size, and soymilk solids were significant determinants of tofu yield (R2 = 0.80). Two variables, soymilk index (SI) and tofu index (TI), were calculated to compare overall suitability of soybean genotypes for soymilk and tofu production. SI was calculated by summing yield, total solids, protein content, and whiteness index of soymilk. TI was calculated by summing yield, protein, whiteness index, and strength of tofu. Seed oil content and size were significant determinants of SI (R2 = 0.41), whereas soymilk color, seed size, and seed protein content were significant determinants of TI (R2 = 0.52). The SI and TI values indicated BARC‐9 to be a desirable genotypes for soymilk and for tofu preparation.

Summary Chickpea is an important food legume and is a major ingredient in many human diets. Chemical composition, physical parameters, functional properties and microstructural characteristics of three kabuli chickpea cultivars and the effects of three cooking methods were investigated. Carbohydrate and protein were two major components in all seeds. Cooking increased fibre, total carbohydrate and total and resistant starch contents, but decreased ash content. Protein and oil levels of the cooked samples either decreased or did not change significantly. Seed weight and density decreased with cooking. Hydration and swelling capacities as well as water absorption and holding capacities of cooked chickpeas were higher than raw samples, with the largest increases in the pressure‐cooked seeds. Seed weights were highly correlated with hydration (r = 0.89) and swelling (r = 0.76) rates. Emulsifying activity, emulsifying stability and foaming capacity of cooked chickpea flours decreased, while foaming stability increased. Chickpea flours had pronounced morphological changes after cooking.