Using cereal crops as examples, we review the breeding for tolerance to the abiotic stresses of low nitrogen, drought, salinity and aluminium toxicity. All are already important abiotic stress factors that cause large and widespread yield reductions. Drought will increase in importance with climate change, the area of irrigated land that is salinized continues to increase, and the cost of inorganic N is set to rise. There is good potential for directly breeding for adaptation to low N while retaining an ability to respond to high N conditions. Breeding for drought and salinity tolerance have proven to be difficult, and the complex mechanisms of tolerance are reviewed. Marker-assisted selection for component traits of drought in rice and pearl millet and salinity tolerance in wheat has produced some positive results and the pyramiding of stable quantitative trait locuses controlling component traits may provide a solution. New genomic technologies promise to make progress for breeding tolerance to these two stresses through a more fundamental understanding of underlying processes and identification of the genes responsible. In wheat, there is a great potential of breeding genetic resistance for salinity and aluminium tolerance through the contributions of wild relatives.

Deep rooting can be inhibited by strong layers, although there is evidence for species and cultivar (cv.) differences in their penetration ability. Here, the availability of near-isogenic lines (NILs) in rice (Oryza sativa L.) was exploited to test the hypothesis that increased root diameter is associated with greater root bending stiffness, which leads to greater root penetration of strong layers. Wax/petrolatum discs (80% strong wax) were used as the strong layer, so that strength can be manipulated independently of water status. It was found that good root penetration was consistently associated with greater root diameter and bending stiffness, whether comparisons were made between cvs or between NILs. With NILs, this effect was seen with ‘research’ lines bred from recombinant inbred lines of a cross between cvs Bala and Azucena and also in improved lines developed from cv. Kalinga III by introgression of parts of the genome from Azucena. Much of the bending behaviour of roots could be explained by treating them as a simple cylinder of material. In both wax disc and sand culture systems, roots that had encountered a strong layer had lower bending stiffness than roots that had not encountered a strong layer which is a novel result and not previously reported.

Since its initial detection in Australia in 1979, wheat yellow (stripe) rust ( Puccinia striiformis f.sp. tritici ) has evolved in Australia and New Zealand into more than 20 pathotypes with assorted virulence characteristics. This evolution is believed to have occurred in a stepwise fashion from an original single pathotype, with no subsequent new introductions. A combination of random amplified polymorphic DNA (RAPDs) and amplified fragment length polymorphisms (AFLPs) was used to examine the level of molecular variation in Australian and New Zealand isolates, and to compare this with variation amongst other isolates of P. striiformis . Using 60 RAPD primers on seven Australian isolates representing seven different pathotypes collected between 1979 and 1991, more than 300 potentially polymorphic loci were analysed and no polymorphisms were detected. Using the same primers on two UK isolates, 3% of loci showed a polymorphism. A similar level of polymorphism was found between UK isolates using AFLP primers, and between 5 and 15% of fragments were polymorphic between an isolate from the UK, an isolate from Denmark, and one from Colombia. However, no AFLP polymorphisms were found amongst 14 Australian and New Zealand isolates tested, at over 100 potentially polymorphic loci. The lack of molecular variation in the Australian and New Zealand collection is consistent with the stepwise mutation theory of pathotype evolution from a single introduction.