The fall armyworm (FAW), Spodoptera frugiperda (J.E. Smith) (Lepidoptera: Noctuidae) is a highly destructive polyphagous pest that primarily damages maize. Maize is considered a most versatile crop for growing intercrops due to the wide row it needs. Maize–pea intercropping is preferred by small and marginal farmers worldwide due to various advantages including higher yield and improved economic benefits. However, the success of this intercropping system may be hampered if pea could sustain the FAW population. Thus, to clarify the fitness and potential effect of S. frugiperda on pea, we analysed the survival and development of S. frugiperda fed on pea leaves in the laboratory and constructed age-stage and two-sex life tables. Results showed that FAW successfully completed its life cycle when fed on pea and produced fertile offspring. The pre-adult duration was significantly higher on pea than maize. The net reproductive rate, intrinsic and finite rate of population increase on pea (135.06 offspring per individual, 0.12 offspring per individual per day and 1.13 times per day) were all significantly different from those on maize (417.64 offspring per individual, 0.19 offspring per individual per day and 1.21 times per day). The probability of survival of S. frugiperda at each stage was lower when fed on pea leaves than that of maize-fed larvae. Due to the overlapping growth periods of the maize and pea, S. frugiperda can easily proliferate throughout the year by shifting between adjacent crops. Thus, this study revealed the adaptability of S. frugiperda for pea and provides the foundation for further assessment of FAW risk to other inter-crops.

In order to gain an understanding of the genetic basis of traits of interest to breeders, the pea varieties Brutus, Enigma and Kahuna were selected, based on measures of their phenotypic and genotypic differences, for the construction of recombinant inbred populations. Reciprocal crosses were carried out for each of the three pairs, and over 200 F2 seeds from each cross advanced to F13. Bulked F7 seeds were used to generate F8–F11 bulks, which were grown in triplicated plots within randomized field trials and used to collect phenotypic data, including seed weight and yield traits, over a number of growing seasons. Genetic maps were constructed from the F6 generation to support the analysis of qualitative and quantitative traits and have led to the identification of four major genetic loci involved in seed weight determination and at least one major locus responsible for variation in yield. Three of the seed weight loci, at least one of which has not been described previously, were associated with the marrowfat seed phenotype. For some of the loci identified, candidate genes have been identified. The F13 single seed descent lines are available as a germplasm resource for the legume and pulse crop communities.

We studied the effectiveness of glyphosate [N-(phosphono-methyl)glycine] for the control of Orobanche spp. in the field when applied to the crop foliage prior to the emergence of the parasite. The best Orobanche control in October-sown carrots (Daucus carota L.) parasitized by Orobanche crenata Forsk. and O. aegyptiaca Pers. and in December-sown broad bean (Vicia faba L.) and peas (Pisum sativum L.) parasitized by O. crenata was obtained by spraying twice, 2 weeks apart, in late January and in February, respectively. Carrot root yield remained unaffected by glyphosate at rates up to 200 g/ha. In heavily infested fields, carrots were irreversibly damaged by early Orobanche parasitism. The highest yields of pods of broad beans occurred after two or three applications of 150 g/ha glyphosate. Peas were seriously damaged by 150 g/ha. Two or three sprays of 50 g/ha glyphosate resulted in the highest green-kernel yield of pea where the soil was not heavily infested. Glyphosate effectively reduced O. cernua Loeffl. emergence in non-irrigated tomatoes (Lycopersicum esculentum Mill.), but was very phytotoxic to the crop. Glyphosate was highly effective in controlling Orobanche spp.; however, marginal selectivity may be sufficient in some crops and not in glyphosate-susceptible ones.

There is little information on the tolerance of leguminous crops to saflufenacil. A field study was conducted three times over a 2-yr period (2006, 2007) in Ontario, Canada, to determine the tolerance of adzuki bean, cranberry bean, lima bean, processing pea, snap bean, soybean, and white (navy) bean to saflufenacil applied PRE at 100 and 200 g ai/ha. Saflufenacil caused 51 to 99% injury, reduced height 25 to 93%, reduced shoot dry weight 92 to 99%, and reduced seed yield 56 to 99% in adzuki bean, cranberry bean, lima bean, snap bean, and white bean. Injury was lower in soybean and processing pea. Saflufenacil caused 1 to 25% injury, reduced height 3 to 13%, reduced shoot dry weight 5 to 30%, and reduced seed yield 0 to 4% in soybean and processing pea. Cranberry bean, snap bean, white bean, and lima bean were the most sensitive crops to saflufenacil followed by adzuki bean. Soybean and processing pea were the most tolerant to saflufenacil. Based on these results, saflufenacil applied PRE can be safely used in specific cultivars of pea and soybean at the proposed rate of 100 g/ha. However, there is not an acceptable margin of crop safety for saflufenacil PRE at 100 or 200 g/ha in adzuki, cranberry, lima, snap, and white bean.

Imazamox is an imidazolinone herbicide being developed for weed control in imidazolinone-resistant wheat (IMI-wheat) cultivars and various legume crops. In a series of studies conducted under a range of dryland cropping environments in the Pacific Northwest United States, imazamox applied to IMI-wheat or pea injured barley and canola grown 1 yr after imazamox treatment in low-rainfall, low–soil pH locations of Oregon. Injury was not observed in higher rainfall locations near Pullman, WA. Non–herbicide-resistant wheat planted 1 yr after IMI-wheat treated with imazamox was not injured. Of particular concern for imazamox carryover are low-rainfall areas with low-pH soils. Reduced soil moisture appears to limit imazamox degradation. Imazamox sorption is reduced in low-pH soils, which increases its bioavailability, thereby increasing the potential for injury to rotational crops such as barley, canola, and spring wheat.

Whole-plant bioassays using sugar beet, lettuce, cucumber, green bean, pea, and soybean as test crops were used to detect mesotrione residues in the soil. The test crops were planted in soil treated with mesotrione in the field the previous year at rates of 0 to 560 g ai ha−1 and in nontreated soil from the same field, with mesotrione added at concentrations of 0 to 320 μg kg−1. Experiments were conducted in the greenhouse for a 21-d period. Values for the dose giving a 50% response (I50) were predicted using a log-logistic nonlinear regression model. I50 values (mean ± SE) of 8.6 ± 1.8, 14.9 ± 2.0, 29.8 ± 11.0, 41.6 ± 7.3, 52.9 ± 6.4, and 67.9 ± 30.3 g ai ha−1 for sugar beet, lettuce, green bean, cucumber, pea, and soybean, respectively, indicate that these crops were effective bioassay test species for quantifying mesotrione residues. A greenhouse bioassay was a simple and sensitive tool to detect mesotrione at concentrations of less than 1.0 μg kg−1 with sugar beet and lettuce being the most sensitive test species. The I50 values for soil treated with known concentrations of mesotrione were lower than for field soil treated with mesotrione the previous year. Knowing the level of mesotrione residues in the soil, growers have flexibility in crop rotations following mesotrione use on corn. Growers can use this information to minimize risk of crop injury by choosing appropriate rotation crops that suffer little or no yield reduction.

Bowman–Birk inhibitors (BBI) from legumes, such as soyabean, pea, lentil and chickpea, are naturally occurring plant protease inhibitors which have potential health-promoting properties within the mammalian gastrointestinal tract. BBI can survive both acidic conditions and the action of proteolytic enzymes within the stomach and small intestine, permitting significant amounts to reach the large intestine in active form to exert their reported anti-carcinogenic and anti-inflammatory properties. In a previous study, we reported the ability of a recombinant form of TI1B (rTI1B), representing a major BBI isoinhibitor from pea, to influence negatively the growth of human colorectal adenocarcinoma HT29 cells in vitro. In the present study, we investigate if this effect is related directly to the intrinsic ability of BBI to inhibit serine proteases. rTI1B and a novel engineered mutant, having amino acid substitutions at the P1 positions in the two inhibitory domains, were expressed in the yeast Pichia pastoris. The rTI1B proved to be active against trypsin and chymotrypsin, showing Ki values at nanomolar concentrations, whereas the related mutant protein was inactive against both serine proteases. The proliferation of HT29 colon cancer cells was significantly affected by rTI1B in a dose-dependent manner (IC50 = 31 (sd 7) μm), whereas the inactive mutant did not show any significant effect on colon cancer cell growth. In addition, neither recombinant protein affected the growth of non-malignant colonic fibroblast CCD-18Co cells. These findings suggest that serine proteases should be considered as important targets in investigating the potential chemopreventive role of BBI during the early stages of colorectal carcinogenesis.

The tribe Fabeae (formerly Vicieae) contains some of humanity's most important grain legume crops, namely Lathyrus (grass pea/sweet pea/chickling vetches; about 160 species); Lens (lentils; 4 species); Pisum (peas; 3 species); Vicia (vetches; about 140 species); and the monotypic genus Vavilovia. Reconstructing the phylogenetic relationships within this group is essential for understanding the origin and diversification of these crops. Our study, based on molecular data, has positioned Pisum genetically between Vicia and Lathyrus and shows it to be closely allied to Vavilovia. A study of phylogeography, using a combination of plastid and nuclear markers, suggested that wild pea spread from its centre of origin, the Middle East, eastwards to the Caucasus, Iran and Afghanistan, and westwards to the Mediterranean. To allow for direct data comparison, we utilized model-based Bayesian Analysis of Population structure (BAPS) software on 4429 Pisum accessions from three large world germplasm collections that include both wild and domesticated pea analyzed by retrotransposon-based markers. An analysis of genetic diversity identified separate clusters containing wild material, distinguishing Pisum fulvum, P. elatius and P. abyssinicum, supporting the view of separate species or subspecies. Moreover, accessions of domesticated peas of Afghan, Ethiopian and Chinese origin were distinguished. In addition to revealing the genetic relationships, these results also provided insight into geographical and phylogenetic partitioning of genetic diversity. This study provides the framework for defining global Pisum germplasm diversity as well as suggesting a model for the domestication of the cultivated species. These findings, together with gene-based sequence analysis, show that although introgression from wild species has been common throughout pea domestication, much of the diversity still resides in wild material and could be used further in breeding. Moreover, although existing collections contain over 10,000 pea accessions, effort should be directed towards collecting more wild material in order to preserve the genetic diversity of the species.

Feeding stem–leaf–pod explants with d-chiro-inositol and d-pinitol was used as a method to modify α-d-galactosides in developing pea (Pisum sativum) seeds. Four genotypes differing in the composition of raffinose, stachyose and verbascose (raffinose family oligosaccharides or RFOs) in seeds – high RFOs (cv. Tiny), low RFOs (SZD175) and low verbascose (cv. Hubal and cv. Wt 506) – were studied. Although seeds of all examined pea lines were able to take up both d-chiro-inositol and d-pinitol, only d-chiro-inositol was effectively converted into its galactosides: mainly fagopyritol B1 (O-α-d-galactopyranosyl-(1 → 2)-d-chiro-inositol) and fagopyritol B2 (O-α-d-galactopyranosyl-(1 → 6)-O-α-d-galactopyranosyl-(1 → 2)-d-chiro-inositol). In seeds of pea lines naturally containing low levels of verbascose (cv. Hubal) and low RFOs (SZD175), the enhanced accumulation of fagopyritols depressed the RFO level by c. 64 and 20%, respectively. Moreover, in both genotypes, about 25 and 30% of total galactose bound in α-d-galactosides occurred in fagopyritols. d-Pinitol present in the pea seeds was converted into monogalactosides, but their accumulation was several-fold lower than that of fagopyritols and did not significantly influence the accumulation of RFOs. Pea seeds with the composition of soluble carbohydrates modified by feeding with either of the cyclitols were able to complete germination.

The variation for protein content has been assessed in a series of pea (Pisum sativum L.) lines differing in mean seed size. The range of seed size within each genotype was manipulated by growing the plants in different environments and by altering the structure of the plant. The response of the lines in terms of seed weight to the environments and treatments was inconsistent, but 90% of the total variation was accounted for by differences between genotypes. In contrast, for percentage protein, the genetic component was much weaker with nearly half the variation being accounted for by within (residual) variation. The correlations between seed weight and percentage protein were highly genotype specific. For the largerseeded genotype, percentage protein increased with increasing seed size (r= +0.9, P < 0.01), while for the small-seeded genotype there was mid-range negative value (r = −0.5, P <0.01). It is suggested that any assessment of percentage protein in pea genotypes must take account of seed size.

Total protein content and amounts of albumin, legumin and vicilin have been determined for pea seeds from lines near-isogenic except for genes at the rugosus loci, r and rb (RR/RbRb; rr/RbRb; RR/rbrb; rr/rbrb). Seeds with the wildtype, round-seeded phenotype (RR/RbRb) had less protein on a total seed dry-weight basis than any of the wrinkled-seeded lines and this protein had a lower proportion of albumin. The lines which had recessive alleles at both r and rb loci had the highest proportion of protein and the highest proportion of albumin. The roundseeded peas possessed nearly two-fold more legumin than the double recessive line, with proportions for the two single recessive lines falling in between these extremes. Vicilin levels were similarfor all four near-isogenic lines. SDS-PAGE analysis of the isolated albumin, legumin and vicilin fractions revealed no significant differences between the four lines. Differential scanning calorimetry of protein extracts showed that all the wrinkled-seeded near-isolines possessed legumin fractions with diminished thermal stability relative to that from the roundseeded, wild-type line.

Chemically-induced mutants were also analysed for protein content and composition. These mutants have previously been shown to display great variation in starch and lipid levels. Total protein varied from 20.3% to 37.9%; however, relative proportions of albumin, legumin and vicilin were similar in all mutant lines. SDS-PAGE analysis identified two mutant pea lines which possessed a legumin A-chain of 65 000 Mr as well as the typical 45 000 Mr form. Differential scanning calorimetry of protein extracts indicated that the legumin in all mutants had lower enthalpies of denaturation than the legumin in the round-seeded parent.

The mutant pea lines possess exceptional variation with respect to starch, lipid and protein which raises opportunities for their use in the food and animal feedstuff industries.

On the premise that seed ageing may be largely a result of free-radical lipid autoxidation, a study was made of the relationship between lipid stability and longevity in seeds of soybean (Glycine max), lentil (Lens culinaris), mungbean (Vigna radiata), chickpea (Cicer arietinum), broadbean (Vicia faba), pea (Pisum sativum), lettuce (Lactuca sativa), and tomato (Lycopersicon esculentum). Seed lipids were examined for α-, γ- and δ-tocopherols, and levels of unsaturated and saturated fatty acids. Using this information, analysis was attempted using linear, multiplicative or exponential models to correlate aspects of lipid stability with seed longevity values from the published literature. No statistically significant correlations could be found between longevity and total lipid unsaturation, tocopherol levels or two protection formulae obtained from the oil chemistry literature. When values for tomato were excluded, a good correlation (r = 0.89, P = 0.007) was obtained using a multiplicative regression model for levels of linolenic acid per unit of total tocopherols in relation to longevity. Possible factors contributing to a lessening of the relationship between lipid stability and seed longevity are discussed.

The value of the garden pea (Pisum sativum) both as an experimental tool and food crop has led to an accumulated wealth of genetic variation. This paper describes how some of the variation may be harnessed for studying seed development. One can identify genotypic differences for maternal, embryonic and cellular components and the interaction between them. The impact of these components on processes such as cell division, partitioning and the deposition of storage products can then be assessed by utilizing new techniques such as immunocytochemistry and in situ hybridization.

The rugosus loci, which induce wrinkling of the seed, are examples of how major genes can be exploited to dissect seed development. Alleles at one of these loci, r, have been defined at both the molecular and biochemical levels. A much clearer picture can now be drawn of the pleiotropic nature of the genes, from their effects on starch composition to those on cellular development, which has implications for seed development in many species. The rugosus loci are the only ones known to affect seed development in peas. By analogy with cereal seeds, however, one would anticipate other mutants in the starch pathway which also affect the shape of the seed. Here, we report the induction of new rugosus-like mutants, compare them to starch mutants in other species and examine the ways in which they may help our understanding of starch biosynthesis and the regulation of seed development.

The raffinose family of oligosaccharides (RFO) is present in relatively high levels in grain legume seeds. They are considered to be antinutritional compounds because they are, at least in part, believed to be responsible for causing flatulence in humans, which is the single most important factor in deterring people from including more legume seeds in their diet. The RFO also have important functions within the plant. They serve as transport metabolites in many legumes and have been proposed to play a positive role in cold acclimatisation and in conferring desiccation tolerance during seed maturation. These responses to environmental stresses are believed to result from the RFO acting as protecting agents for membrane bound-proteins. We have screened 70 pea lines from the test array of the John Innes Pisum germplasm collection, and lines were selected which had unusual RFO composition. The soluble sugars within these lines were quantified using High Performance Anion Exchange Chromatography with Pulsed Amperometric Detection (HPAEC-PAD), and variants were identified which were deficient in verbascose and one with a reduced level of raffinose. These selected lines are being used in a crossing programme designed to study the genetics of the RFO pathway and to produce new material to test the effect of specific RFO on the plant’s responses to the environment and on the diets of humans and animals.

Disease resistance, increased crop residues and altered plant and canopy design are the primary strategies being used to solve the major problems of cool season food legumes that are an integral component of cropping systems in the rainfed areas of the U.S. Pacific Northwest. Dry pea, seed pea and lentil predominate among these legumes, but there is increasing interest in chickpea. Several diseases are major hazards to production, including root rots, wilts, powdery mildew, Ascochyta blight, and viruses. Pea and lentil cultivan resistant to root rots, wilts, and powdery mildew are being developed and released. Progress is being made on resistance to v iruses transmitted by aphids, including pea enation mosaic and bean leaf roll. Development of res istant cultivars has been the principal control strategy for several diseases: Ascochyta blight of chickpea and lentil; root rots and wilts of pea, lentil, and chickpea; powdery mildew of pea; and viruses of pea and lentil. Chickpea cultivars resistant to Ascochyta blight were recently made avallable to producers. Another problem is that crop residues are insufficient to control erosion. Research is underway on genetically increasing biomass and residue production in lentil and dry pea and on producing more lignified stems and other plant parts that are more resistant to breakdown during harvesting and subsequent tillage. Increased biomass also might increase grain yields and red uce harvesting losses. The semi-leafless and woody stem traits in pea, the bushy plant types of lentil and chickpea, and diverse pod traits in all the legumes have shown promise for increased yield potential, ease of harvest, and reduced shattering losses.