Whitefly, Bemisia tabaci, is one of the most important pests of tomato, Solanum lycopersicum L. The Mi-1 gene mediates tomato resistance to the Middle East-Asia Minor 1 (MEAM1) and Mediterranean (MED) species of B. tabaci, three species of root-knot nematodes, Meloidogyne spp., and the potato aphid, Macrosiphum euphorbiae. Tomato seedlings bearing the Mi-1 gene are resistant to nematodes soon after germination but resistance to aphids is developmentally regulated; a reliable conclusion about Mi-1 resistance to B. tabaci was not available to date. In the present work, 3-, 5- and 8-week-old plants of the tomato cultivars Motelle and Moneymaker (bearing and lacking the Mi-1 gene, respectively) were simultaneously tested under free-choice (antixenosis) and no-choice (antibiosis) conditions, to assess the real influence of plant age on the Mi-1-mediated resistance to the MED species of B. tabaci. Subsequently, plants of the same age but with different level of development were compared to check whether the plant size can also affect this tomato resistance. Obtained results demonstrated that Mi-1-mediated resistance to B. tabaci is developmentally regulated, as variations in the age of bearing-Mi-1 plants affects most infestation parameters tested. Differences between cultivars with and without the Mi-1 gene were significant for 8- but not for 3-week-old plants. For 5-week-old plants, differences between cultivars were less pronounced than in older plants, expressing an intermediate level of resistance in Motelle. Plant size also influenced whitefly infestation and reproductive activity on the resistant cultivar. However, plant age has more impact than plant size on the Mi-1-mediated resistance of tomato to B. tabaci.

Laboratory and field trials were conducted to evaluate the effect of plant species (maize, sorghum), plant age (young, middle, old) and four different nitrogen fertilization levels (N0–N3) on the bionomics of the invasive crambid Chilo partellus and the performance of its braconid larval parasitoid Cotesia flavipes. Plant N varied significantly between N0 and N1–N3, but the differences among the latter were not significant. Intrinsic rates of increase and net-reproductive rates of C. partellus followed the same trends: they were lowest with N0 and similar among the other treatments. On maize only, mortality of C. partellus and parasitism by C. flavipes tended to decrease with age of the plant while the percentage of borers reaching adulthood (i.e. pupation) increased. Borer mortality and parasitism was lower and pupation higher on sorghum than on maize. On both host plants, percent dry matter content of frass, which could affect ingress of the parasitoid into the borer tunnel, did not vary with nitrogen level but varied with age of the host plants: on maize, it was highest on young plants and on sorghum on old plants. Tunnels were shorter on young maize and sorghum plants; longer tunnels on older plants indicated compensatory feeding by the larva as a result of lower nutritive value of the food source. Consequently, larval weight was lower on older than younger plants. The level of nitrogen fertilization had no effect on food conversion efficiency of C. partellus. Nitrogen did not affect number of C. flavipes progeny while egg load of progeny increased significantly with nitrogen level, on both plant species. Differences in egg load between sorghum and maize were mostly not significant. It was concluded that on depleted soils only, an increase in nitrogen via mulching, rotation with a leguminous crop or fertilization would increase survival of C. partellus on both maize and sorghum and an increase in acreage of maize and in application of nitrogen fertilizer in an area would also increase the parasitism of C. flavipes.

Potted subterranean clover (Trifolium subterraneum) plants of different ages were exposed to 70 nl l−1 ozone for 6 h, either during the light or during the dark period in a laboratory-based climate chamber. There was limited visible leaf injury on plants which were 14–20 and 28–34 d old and no significant decrease in biomass after daytime ozone exposure. The oldest leaves of 22–26 d old plants exhibited severe visible injury, which was associated with a significant reduction in biomass in 24–26 d old plants. Thus, ozone-induced visible injury of different magnitude developed in all plants, but was associated with biomass reduction only during a limited period of the plant's life-span. Apart from modifying ozone uptake by plants, climatic conditions are important as growth modifiers. It is suggested that subterranean clover plants of defined developmental stages should be used in bioindication of ozone. Night ozone exposure injured significantly fewer leaves than day exposure. However, some leaves developed visible injury even after night ozone exposure. Night uptake of ozone may be of more importance in northern than in central and southern Europe, because summer nights are short and, for a certain period, never completely dark.

The aim of this work was to examine the correspondence between apoplastic/symplastic antioxidant status and previously reported plant age-related shifts in the ozone (O3) resistance of Plantago major L. Seed-grown plants were fumigated in duplicate controlled environment chambers with charcoal/Purafil®-filtered air (CFA) or CFA plus 70 nmol mol−1 O3 for 7 h d−1 over a 42 d period. Measurements of stomatal conductance and antioxidants were made after 14, 28 and 42 d fumigation, on leaves at an equivalent stage of development (youngest fully expanded leaf, measured c. 9 d after emergence). Ozone exposure resulted in a similar decline in stomatal conductance across plant ages, indicating that increases in O3 resistance with plant age were mediated through changes in the tolerance of leaf tissue rather than enhanced pollutant exclusion. Leaf apoplastic washing fluid was found to contain ‘unspecific’ peroxidase, ascorbate peroxidase, superoxide dismutase and ascorbate, but not glutathione and the enzymes required to facilitate the regeneration of ascorbate from its oxidized forms. A weak induction in the activity of certain symplastic antioxidants was found after 14 d O3 fumigation, despite a lack of visible symptoms of injury, but shifts in symplastic antioxidant enzyme activity were not consistent with previously observed increases in resistance to O3 with plant age. By contrast, changes in ‘unspecific’ peroxidase activity and in the small pool of ascorbate in the leaf apoplast were found to accompany age-related shifts in O3 resistance. It is concluded that constituents of the leaf apoplast may constitute a potentially important front line defence against O3.

The impact of O3 at different stages of plant development was investigated in growth-chamber-cultivated Plantago major L. Six-d-old plants of an O3-sensitive population (‘Valsain’) were exposed to one of the following six treatments; 56 d charcoal/Purafil®-filtered air (CFA): 56 d CFA plus 70 nmol mol−1 O3 for 7 h d−1; CFA with a 14-d episode of O3 administered at days 1, 14, 28 or 42. Harvests were made every 14 d, and at the final harvest (56 d) the influence of O3 on reproductive structures was assessed.

Analysis of the effects of O3 on growth and reproductive performance confirmed the sensitivity of the population to the pollutant. In the absence of the development of typical visible symptoms of foliar damage, the total d. wt of plants maintained in O3 over a 56-d period was 35% lower than that of control plants. However, the impact of the pollutant was found to decrease as plants aged. Plant relative growth rate (R) was only affected in seedlings, suggesting that effects of O3 on seedling growth were largely responsible for the decrease in accumulated biomass; the growth rate of older plants was not affected by O3. The observed shift in O3 resistance with plant age was mediated by both ‘acclimation’ and ontogenetic changes. ‘Acclimation’ was not associated with changes in O3 uptake, and there was some evidence to support the existence of compensatory growth responses. In addition to effects on vegetative growth, plants exhibited an O3-induced decline in reproductive performance; O3 reducing the number of flower spikes and seed capsules produced per plant. Ozone episodes administered at different stages of development indicated that reproductive development was particularly sensitive to O3 during the early stages of flowering.

The findings of this study are discussed in relation to evolutionary adaptation to O3 in natural plant communities.The importance of plant age, prior exposure to the pollutant and the timing of O3 episodes in relation to plant developmental stage are highlighted.

Factors contributing to host plant resistance in sorghum to Chilo partellus (Swinhoe) were studied. Oviposition on the plants in the field started 3 weeks after germination and peaked 2–6 weeks later. Egg batches (96.1%) were laid on the leaf blades compared with 3.9% on the leaf sheaths. On the leaf blades, significantly more egg batches were laid on the upper (57.2%) than on the lower leaf surfaces. In young plants, leaves attached to the upper and lower segments were preferred for oviposition, while leaves in the upper segments more or less maintained their share of egg batches over time; there was a shift from the leaves in the lower to those in the middle segments with the plant age. Differences among sorghum lines for oviposition were significant and these lines were divided into three categories based on their levels of oviposition.

Sorghum plants reacted to insect feeding in the stem by production of a red staining compound which did not significantly affect the development of the insect. Four damage symptoms were observed and these were related to different plant ages. Plants compensated damage by the production of extra tillers, some of which produced panicles that were ready by approximately the time of harvest. Plants infested 2 weeks after germination produced maximum tillers and juvenile panicles; and also had the least effective tillers, plant heights and grain yields. Grain yields were depressed in the infested plants for the cultivars tested, except in LC 119/80–3 where there were actual grain yield gains.

Leaf-feeding and ‘dead heart’ scores, which were related to reduced plant heights and yields in some of the cultivars tested, are proposed as rational indices for susceptibility ratings and monitoring of crop losses.