In field and greenhouse experiments, liquid or granular formulations of EPTC (S-ethyl dipropylthiocarbamate) applied by hand directly in the row with seed of alfalfa (Medicago sativa L. ‘Vernal’), controlled grass seedlings in bands, usually 5 to 8 cm wide, without injuring alfalfa significantly. Grass was similarly controlled selectively when a mixture of alfalfa seed and clay granules, similar in size to alfalfa seed and containing 10% EPTC, was seeded mechanically.

The effect of soil disinfestation with methyl bromide (MB) or by soil solarization (solar heating) and the fungicides TMTD (tetramethylthiuram disulfide) and fentin acetate (triphenyltin acetate) on the degradation of terbutryn [2-(tert-butylamino)-4-(ethylamino)-6-methylthio)-s-triazine] and atrazine [2-chloro-4-(ethylamino)-6-(isopropylamino)-s-triazine] were investigated. The degradation of terbutryn appeared to follow first-order kinetics with a half-life of about 2 weeks and was much slower in MB-treated or solarized soils, i.e. half-life of about 11 weeks. Suppression of terbutryn degradation in the MB-treated soil was still evident 8 months after soil fumigation, similar to that found in autoclaved soil. TMTD and fentin acetate at 20 μg/g soil strongly inhibited degradation of terbutryn in soil. Degradation of atrazine was affected to a lesser extent by soil disinfestation. Results from the present study suggest that biocidal soil treatments may slow herbicide degradation. Thus, herbicide dosages in disinfested soil should be adjusted in order to avoid phytotoxicity. Moreover, lower dosages might be sufficient to attain weed control, and combined disinfestation or fungicides with herbicide treatments might be intentionally used to extend herbicide activity.

A sorghum-sudangrass hybrid [Sorghum bicolor (L.) Moench. x Sorghum sudanense (P.) Stapf. ‘DEKALB SX17+’] (SSH) and foxtail millet [Setaria italica (L.) Beauv.] (FM) were evaluated for their effects on weed populations when grown for forage and as land conditioners prior to late-summer, no-till planting of alfalfa (Medicago sativa L. ‘Arc’). Both grasses established well in no-till situations, except for FM when excessive mulch impeded seed placement or seedling summer-annual weeds were not destroyed at planting time. SSH was the better competitor; after both were planted into a dense stand of seedling summer-annual weeds, SSH outyielded the weeds while FM did not. Both grasses suppressed weeds and enhanced subsequent alfalfa establishment. Obtaining adequate alfalfa stands was not a problem in no-till seedings: seedling populations often exceeded 300/m2 3 to 6 weeks after planting. Lack of adequate weed control was associated with stand losses in which disease was also a factor. Biennial and perennial broadleaf species were the predominant weeds. Prior cropping of SSH or FM is a valuable option for growers wishing to establish alfalfa without tillage, particularly when summer forage is useful.

Foxtail millet (Setaria italica (L.) P. Beauv.) is an ideal crop for changing climate and food habits of peoples due to its short duration, high photosynthetic efficiency, nutritional richness and fair resistance to pest and diseases. However, foxtail millet yields are low mainly due to the lack of effort for its improvement and the lack of proper utilization of existing genetic variability. To enhance the use of diverse germplasm in breeding programmes, a core collection in foxtail millet consisting of 155 accessions was established. Core collection accessions were fingerprinted using 84 markers (81 simple sequence repeats (SSRs) and three Expressed Sequence Tag (EST)-SSRs). Our results showed the presence of greater molecular diversity in the foxtail millet core collection. The 84 markers detected a total of 1356 alleles with an average of 16.14 alleles (4–35) per locus. Of these, 368 were rare alleles, 906 common alleles and 82 the most frequent alleles. Sixty-one unique alleles that were specific to a particular accession and useful for germplasm identification were also detected. In this study, the genetic diversity of foxtail millet was fairly correlated well with racial classification, and the race Indica showed a greater genetic distance from the races Maxima and Moharia. The pairwise estimate of dissimilarity was >0.50 except in 123 out of 11,935 pairs which indicated a greater genetic variability. Two hundred and fifty pairs of genetically most diverse accessions were identified. This large molecular variation observed in the core collection could be utilized effectively by breeders or researchers for the selection of diverse parents for breeding cultivars and the development of mapping populations.

Early farming in northern China featured the cultivation of two species of millet, broomcorn and foxtail. Although previously seen as focused on the Yellow River, the authors show that the earliest agriculture is actually found in the foothills of the neighbouring mountain chains, where drier and better drained locations suited millet cultivation, particularly broomcorn. In this they echo new thoughts on the locale of early agriculture in south-west Asia, on the hilly flanks of the Fertile Crescent rather than in the valleys of the Nile or the Euphrates.

Foxtail millet (Setaria italica (L.) Beauv.) is one of the ten small millets and is cultivated in 23 countries. The foxtail millet is valued as a crop of short duration, which is good as food, feed and fodder. In general, grain yield levels of foxtail millet are low in comparison with other staple cereals. The greater use of diverse germplasm in breeding is suggested as a means to improve the productivity of this crop. The International Crops Research Institute for the Semi-Arid Tropics genebank is presently holding 1474 cultivated germplasm accessions from 23 countries. To utilize this diversity in research, a core collection (10% of the entire collection) was established using the taxonomic and qualitative traits data. The germplasm accessions were stratified into three taxonomic races (Indica, Maxima and Moharia). Principal coordinate analysis was performed on 12 qualitative traits for each of the biological races, separately that resulted in the formation of 29 clusters. From each cluster, 10% of the accessions were selected to constitute a core collection of 155 accessions. The composition and diversity of the core collection was validated by the χ2-tests of the frequencies of origin, races, subraces and data on qualitative traits. The analysis of the quantitative traits for mean, range, variance, Shannon–Weaver diversity index and phenotypic associations indicated that the diversity from the entire collection was optimally represented in the core collection. The core subset will be evaluated in replicated trials to make a more precise assessment of diversity and further efforts to identify the sources of agronomic and grain nutritional traits for utilization in breeding programmes.