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Plants display an array of classical strategies to maximize phosphate (Pi) acquisition from sparingly soluble P sources. Acclimation to Pi-stress via elegant Pi-starvation induced (PSI) adjustments would reduce our current overreliance on expensive, polluting and non-renewable Pi-fertilizers. Nevertheless, differences in the ability of various species to solubilize sparingly soluble P-sources have been often evidenced; inter-cultivar variations are scarcely documented. Brassica is known as an effective, non-mycorrhizal user of sparingly soluble P-sources. Various growth parameters and biomass accumulation by genetically diverse Brassica cultivars were determined in four experiments using hydroponics and quartz sand culture media. Role of PSI root mediated pH changes, organic anions (OAs) exudation and altered root architecture in mobilization and acquisition of sparingly soluble P-forms [Jordan rock-P (RP) at 2 g l )1 and Ca 3 (PO 4 ) 2 (TCP) at 0.2 g l )1 respectively] was investigated. Cultivars showed considerable genetic variations in biomass accumulation, various growth parameters and root-shoot ratio. Concentration and total uptake of P, specific absorption rate of P, P-transport rate and P-utilization efficiency (PUE) were also significantly (P < 0.001) different for various cultivars and their dry matter was significantly correlated with P-uptake [r = 0.94** (significant at 1% level)]. P-tolerant cultivars showed substantial decrease in solution media pH because of H + efflux and exuded more carboxylates than low P-sensitive cultivars under P-starvation. P-uptake by cultivars increased linearly with decreasing pH. The amount and types of OAs exuded from the roots of P-starved plants differed from those of plants grown under P-sufficient environment. In split pot study, with TCP and RP supplied spatially separated from other nutrients, efficient cultivars were still able to mobilize RP and TCP more efficiently than inefficient cultivars. In rhizobox study, the elongation rates of primary roots decreased but the elongation rates of the branched zones of primary roots and the length of lateral roots increased under P-starvation. Tested cultivars showed genetic diversity in accessing, mobilization, acquisition and utilization of Pi from sparingly soluble P forms. An arrange marriage of plant traits can explain cultivar's access to different forms of sparingly soluble P, and in addition to altered lateral root topology and enhanced P-uptake and PUE, enhanced H + efflux and OAs exudation are key factors in Pi scavenging from extra cellular sparingly soluble P-forms.

The larvae of Plutella xylostella were fed on five wild crucifers, Capsella bursa‐pastoris, Lepidium virginicum, Cardamine flexuosa, Rorippa indica, R. islandica and a crop, cabbage. The developmental period of the immature stages, adult longevity, preoviposition period, fecundity and morphometrical characters of the adults were measured. The flight activity of the adults was also measured by the tethered flight method. All the wild plants except for R. islandica were less suitable host plants than cabbage, and larvae which were fed on these less suitable plants emerged as smaller adults with shorter wings. The smaller female adults had lower fecundity but a higher flight activity. Smaller adults measured in terms of their pupal weight among individuals fed on the same host plant had longer wings. These smaller adults with longer wing flew more actively.

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Translocation of absorbed phosphorus (P) from metabolically inactive sites to active sites in plants growing under P deprivation may increase its P utilization efficiency (PUE). Acclimation to phosphate (Pi) starvation may be caused by a differential storage pool of vacuolar P, its release, and the intensity of re-translocation of absorbed P as P starvation inducible environmental cues (PSIEC) from ambient environment. Biomass assay and three P forms, namely inorganic (Pi), organic (Po), and acid-soluble total (Ptas) were estimated in Brassica cultivars exposed to 10 d P deprivation in the culture media. Considering that -delta Pi/delta t denotes the rate of Pi release, Pi release velocity (RSPi) was determined as the tangent to the equations obtained for Pi f(t) at the mean point in the period of greatest Pi decrease, whereas the inverse of the RSPi was an estimate of the internal Pi buffering capacity (IBCPi). Inter cultivar variations in size of the non-metabolic Pi pool, RSPi, re-translocation of Pi from less to more active metabolic sites, and preferential Pi source and sink compartments were evaluated under P starvation. The cultivar 'Brown Raya' showed the highest Pi storage ability under adequate external P supply, and a more intensive release than 'Rain Bow' and 'Dunkled' under P stress. Cultivar 'B.S.A' was inferior to 'Con-1' in its ability to store and use Pi. Roots and upper leaves were the main sink of Pi stored in the lower and middle leaves of all cultivars and showed lower IBCPi and larger RSPi values than lower and middle leaves. In another trial, six cultivars were exposed to P-free nutrition for 29 d after initial feeding on optimum nutrition for 15 d. With variable magnitude, all of the cultivars re-translocated P from the above ground parts to their roots under P starvation, and [P] at 44 d after transplanting was higher in developing leaves compared with developed leaves. Under P deprivation, translocation of absorbed P from metabolically inactive to active sites may have helped the tolerant cultivars to establish a better rooting system, which provided a basis for tolerance against P starvation and increased PUE. A better understanding of the extent to which changes in the flux of P absorption and re-translocation under PSIEC will help to scavenge Pi from bound P reserves and will bring more sparingly soluble P into cropping systems and obtain capitalization of P reserves.