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• Background Global phosphorus (P) reserves are being depleted, with half-depletion predicted to occur between 2040 and 2060. Most of the P applied in fertilizers may be sorbed by soil, and not be available for plants lacking specific adaptations. On the severely P-impoverished soils of south-western Australia and the Cape region in South Africa, non-mycorrhizal species exhibit highly effective adaptations to acquire P. A wide range of these non-mycorrhizal species, belonging to two monocotyledonous and eight dicotyledonous families, produce root clusters. Non-mycorrhizal species with root clusters appear to be particularly effective at accessing P when its availability is extremely low.• Scope There is a need to develop crops that are highly effective at acquiring inorganic P (Pi) from P-sorbing soils. Traits such as those found in non-mycorrhizal root-cluster-bearing species in Australia, South Africa and other P-impoverished environments are highly desirable for future crops. Root clusters combine a specialized structure with a specialized metabolism. Native species with such traits could be domesticated or crossed with existing crop species. An alternative approach would be to develop future crops with root clusters based on knowledge of the genes involved in development and functioning of root clusters.• Conclusions Root clusters offer enormous potential for future research of both a fundamental and a strategic nature. New discoveries of the development and functioning of root clusters in both monocotyledonous and dicotyledonous families are essential to produce new crops with superior P-acquisition traits. [ABSTRACT FROM AUTHOR]

Storage of phosphorus (P) in stem tissue is important in Mediterranean Proteaceae, because proteoid root growth and P uptake is greatest during winter, whereas shoot growth occurs mostly in summer. This has prompted the present investigation of the P distribution amongst roots, stems, and leaves of Hakea prostrata R.Br. (Proteaceae) when grown in nutrient solutions at ten P‐supply rates. Glasshouse experiments were carried out during both winter and summer months. For plants grown in the low‐P range (0, 0.3, 1.2, 3.0, or 6.0 µmol d–1) the root [P] was > stem and leaf [P]. In contrast, leaf [P] > stem and root [P] for plants grown in the high‐P range (6.0, 30, 60, 150, or 300 µmol P d–1). At the highest P‐supply rates, the capacity for P storage in stems and roots appears to have been exceeded, and leaf [P] thereafter increased dramatically to approximately 10 mg P g–1 dry mass. This high leaf [P] was coincident with foliar symptoms of P toxicity which were similar to those described for many other species, including non‐Proteaceae. The published values (tissue [P]) at which P toxicity occurs in a range of species are summarized. X‐ray microanalysis of frozen, full‐hydrated leaves revealed that the [P] in vacuoles of epidermal, palisade and bundle‐sheath cells were in the mM range when plants were grown at low P‐supply, even though very low leaf [P] was measured in bulk leaf samples. At higher P‐supply rates, P accumulated in vacuoles of palisade cells which were associated with decreased photosynthetic rates. [ABSTRACT FROM PUBLISHER]