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Notes: When grown at a low P supply, Hakea prostrata R.Br. (Proteaceae) develops dense clusters of determinate branch roots, termed ‘proteoid’ or ‘cluster’ roots and accumulates Mn in its leaves. The aim of this study was to vary the production of cluster roots and assess the relationship between Mn uptake and cluster-root mass. We collected native soil from a location inhabited by H. prostrata and amended this with ‘high’ and ‘low’ amounts of insoluble or soluble P. After 14 months, we measured the impact of the treatments on cluster-root development and the [P], [Mn], [Fe], [Zn] and [Cu] in young (expanding) and mature leaves. Dry mass and leaf area increased with increasing P availability in the soil, but growth decreased at the highest soluble [P], which caused symptoms of P toxicity. The [P] in young leaves (1.3–2.7 mg g−1 DM) exceeded that in older leaves (0.28–0.85 mg g−1 DM), except when plants were grown with soluble P (3.2–21 mg g−1 DM). Cluster-root formation was inhibited when leaf [P] increased; [P] in young leaves, rather than that in old leaves, appeared to be the factor that determined the proportion of the root mass invested in cluster roots. Old leaves of all treatments had [Mn] from 90 to 120 µg g−1 DM, except for plants grown at high levels of soluble P, when [Mn] decreased below 30 µg g−1 DM. The [Mn] and [Zn] in old leaves and the [Cu] in young leaves were positively correlated with the fraction of roots invested in cluster roots. These findings support our hypothesis that cluster roots play a significant role in micronutrient acquisition, and also provide an explanation for Mn accumulation in leaves of H. prostrata, and presumably Proteaceae in general.

Notes: We investigated how the differences in growth and morphology, between fast-growing wildtype (Wt) tomato (Solanum lycopersicum L.) plants and slow-growing gibberellin (GA) deficient W335 mutants, were reflected in cell numbers and cell sizes. We also studied whether the differences between the Wt and the low-GA mutant would persist at a growth-limiting supply of nitrate. Both a low endogenous GA concentration and a low supply of nitrate reduced the number and size of leaf cells, whereas they increased the size and number of root cortex cells. The effects of low N-supply on the size and number of leaf and root cells did not depend on endogenous GA concentrations. The mutant's higher allocation to roots seemed to be the result of the strongly reduced growth of the shoot.

Notes: The growth-promoting effects of gibberellins (GAs) on plants are well documented, but a complete growth analysis at the whole plant level on plants with an altered GA biosynthesis has never been reported. In the present work, the relative growth rate (RGR), biomass partitioning and morphological parameters of wildtype (Wt) tomato (Solanum lycopersicum L. cv. Moneymaker) plants were compared with those of isogenic (gib) mutants with a reduced biosynthesis of gibberellins. GA deficiency reduced RGR and specific leaf area (SLA, leaf area per unit leaf mass) and increased the net assimilation rate (NAR, the rate of biomass increment per unit leaf area). Despite the free access to nitrogen in the rooting medium, the low-GA mutants had a much higher root mass ratio (RMR, the root mass per unit plant biomass) than the Wt, suggesting that the mutants were disturbed in their growth response to nitrate supply. The experiment was repeated at a low exponential nitrate supply, which forced all plants to grow at the same low RGR. The persistence of the differences in RMR at low N-supply indicated that the high RMR of the mutants was a direct effect of low GA, which was independent of nitrate supply. Because the low N-supply increased the RMRs of all genotypes to the same extent, the response of RMR to N-supply does not seem to depend on GA. Although many of the traits of the slow growing GA mutants were very similar to those of inherently slow growing plant species from unproductive habitats, gibberellins are unlikely to be a main determinant of a plant's potential RGR.

Notes: The present authors have shown previously that both respiration rates and in vivo activities of the alternative oxidase (AOX) of leaves of Alocasia odora, a shade species, are lower than those in sun species, thereby optimizing energy production under limited light conditions (Noguchi et al., Australian Journal of Plant Physiology 28, 27–35, 2001). In the present study, mitochondria isolated from A. odora leaves were examined in order to investigate the biochemical basis for the differences in respiratory parameters. Alocasia odora and spinach plants were cultivated under both high and low light intensities, mitochondria were isolated from their leaves, and their respiratory properties compared. Mitochondrial content of leaf extracts from the two species was estimated using fumarase activities and antibody detection of porin (the voltage-dependent anion channel of the outer mitochondrial membrane). On a mitochondrial protein basis, spinach leaves showed higher capacities of the cytochrome pathway and cytochrome c oxidase (COX) than A. odora leaves. However, on a mitochondrial protein basis, A. odora showed higher capacities of AOX, which had a high affinity for ubiquinone when activated by pyruvate. Alocasia odora also had larger amounts of mitochondrial protein per leaf dry weight, even under severely shaded conditions, than spinach. Lower growth light intensity led to lower activities of most pathways and proteins tested in both species, especially glycine-dependent oxygen uptake. In the low light environment, most of the AOX protein in A. odora leaves was in its inactive, oxidized dimer form, but was converted to its reduced active form when plants were grown under high light. This shift may prevent over-reduction of the respiratory chain under photo-oxidative conditions.

Notes: Abstract A brief survey of the biochemistry of the alternative oxidative pathway (‘cyanide-resistant respiration’) and its occurrence in vivo is given. Several hypotheses about the physiological significance of the alternative chain are discussed. These include a role in (1) heat production, (2) fruit ripening, (3) respiration of plants that contain high levels of cyanogenic glycosides, producing HCN upon wounding, (4) oxidation of NADH that is produced by various causes in excess of that required for ATP production, (5) ion uptake, and (6) osmoregulation.In intact roots of higher plants, the activity of the alternative pathway is more active when less carbohydrate is required for assimilation of N (NH+4 NO-3 or N2) and is less active in those when carbohydrates are being stored in a storage organ or when the availability of photosynthate is reduced. An increase in carbohydrate requirement for osmoregulation is also correlated with decreased alternative chain activity.It is concluded that the alternative pathway in roots plays an important role in oxidation of sugars which are not required for carbon skeletons, energy production for growth and maintenance processes, osmoregulation or storage. However, the significance of this role may vary in different tissues and physiological states.

Notes: The use of fossil fuel is predicted to cause an increase of the atmospheric CO2 concentration, which will affect the global pattern of temperature and precipitation. It is therefore essential to incorporate effects of temperature and water supply on carbon partitioning of plants to predict effects of elevated [CO2] on growth and yield of Triticum aestivum.Although earlier papers have emphasized that elevated [CO2] favours investment of biomass in roots relative to that in leaves, it has now become clear that these are indirect effects, due to the more rapid depletion of nutrients in the root environment as a consequence of enhanced growth. Broadly generalized, the effect of temperature on biomass allocation in the vegetative stage is that the relative investment of biomass in roots is lowest at a certain optimum temperature and increases at both higher and lower temperatures. This is found not only when the temperature of the entire plant is varied, but also when only root temperature is changed whilst shoot temperature is kept constant. Effects of temperature on the allocation pattern can be explained largely by the effect of root temperature on the roots' capacity to transport water. Effects of a shortage in water supply on carbon partitioning are unambiguous: roots receive relatively more carbon.The pattern of biomass allocation in the vegetative stage and variation in water-use efficiency are prime factors determining a plant's potential for early growth and yield in different environments. In a comparison of a range of T. aestivum cultivars, a high water-use efficiency at the plant level correlates positively with a large investment in both leaf and root biomass, a low stomatal conductance and a large investment in photosynthetic capacity. We also present evidence that a lower investment of biomass in roots is not only associated with lower respiratory costs for root growth, but also with lower specific costs for ion uptake. We suggest the combination of a number of traits in future wheat cultivars, i.e. a high investment of biomass in leaves, which have a low stomatal conductance and a high photosynthetic capacity, and a low investment of biomass in roots, which have low respiratory costs. Such cultivars are considered highly appropriate in a future world, especially in the dryer regions. Although variation for the desired traits already exists among wheat cultivars, it is much larger among wild Aegilops species, which can readily be crossed with T. aestivum. Such wild relatives may be exploited to develop new wheat cultivars well-adapted to changed climatic conditions.

Notes: We have investigated the water use efficiency of whole plants and selected leaves and allocation patterns of three wheat cultivars (Mexipak, Nesser and Katya) to explore how variation in these traits can contribute to the ability to grow in dry environments. The cultivars exhibited considerable differences in biomass allocation and water use efficiency. Cultivars with higher growth rates of roots and higher proportions of biomass in roots (Nesser and Katya) also had higher leaf growth rates, higher proportions of their biomass as leaves and higher leaf area ratios. These same cultivars had lower rates of transpiration per unit leaf area or unit root weight and higher biomass production per unit water use. They also had higher ratios of photosynthesis to transpiration, and lower ratios of intercellular to external CO2 partial pressure. The latter resulted from large differences in stomatal conductance associated with relatively small differences in rates of photosynthesis. There was little variation between cultivars in response to drought, and differences in allocation pattern and plant water use efficiency between cultivars as found under well-watered conditions persisted under dry conditions. At the end of the non-watered treatment, relative growth rates and transpiration rates decreased to similar values for all cultivars. High ratios of photosynthesis to transpiration, and accordingly high biomass production per unit of transpiration, is regarded as a favourable trait for dry environments, since more efficient use of water postpones the decrease in plant water status.

Notes: Two populations of Lolium perenne L. S23 (perennial ryegrass), selected for differences in mature leaf dark respiration, were used in a non-destructive indexing system for individual plants, to determine growth parameters. Population GL66, selected for high respiratory rates and low yield, responded strongly to the indexing treatment, when grown at low plant density. Dry weights of all plant parts decreased strongly, as did dry matter percentages of the leaf blades. At high density this population demonstrated the same trend, but additionally allocation to the shoot increased. In contrast, GL72, selected for low respiratory rates and a high yield, responded only at a high plant density. It is argued that there might be a relation between the dissimilar response of the two populations to mechanical influences and the presence of the genotypes of the low-yielding population in the parent variety. The results also emphasize that non-destructive growth analyses can only be used when their effects on the plants are known.

Notes: van der Werf, A., Kooijman, A., Welschen, R. and Lambers, H. 1988. Respiratory energy costs for the maintenance of biomass, for growth and for ion uptake in roots of Carex diandra and Carex acutiformis. - Physiol. Plant. 72: 483–491.The respiratory characteristics of the roots of Carex diandra Schrank and Carex acutiformis Ehrh. were investigated. The aims were, firstly to determine the respiratory energy costs for the maintenance of root biomass, for root growth and for ion uptake, and secondly to explain the higher rate of root respiration and ATP production in C. diandra.The three respiratory energy components were derived from a multiple regression analysis, using the relative growth rate and the net rate of nitrate uptake as independent variables and the rate of ATP production as a dependent variable. Although the rate of root respiration and ATP production was significantly higher in C. diandra than in C. acutiformis, the two species showed no significant difference in their rate of ATP production for the maintenance of biomass, in the respiratory energy coefficient for growth (the amount of ATP production per unit of biomass produced) and the respiratory energy coefficient for ion uptake (amount of ATP production per unit of ions absorbed). It is concluded that the higher rate of root respiration of C. diandra is caused by a higher rate of nitrate uptake. At relatively high rates of growth and nitrate uptake, the contribution of the rate of ATP production for ion uptake to the total rate of ATP production amounted to 38 and 25% for C. diandra and C. acutiformis, respectively. At this growth rate, the respiratory energy production for growth contributed 37 and 50%, respectively, to the total rate of ATP production. The relative contribution of the rate of ATP production for the maintenance of biomass increased from 25 to 70% with increasing plant age for both species. The results suggest that ion uptake is one of the major sinks for respiratory energy in roots.These experimentally derived values for the rate of ATP production for the maintenance of biomass, the respiratory energy coefficient for growth and the respiratory energy coefficient for ion uptake are discussed in relation to other experimentally and theoretically derived values.

Notes: Møller, I. M., Bérczi, A., van der Plas, L. H. W. and Lambers, H. 1988. Measurement of the activity and capacity of the alternative pathway in intact plant tissues: Identification of problems and possible solutions. - Physiol. Plant. 72: 642–649.The cyanide-insensitive, benzhydroxamic acid-sensitive (e.g. salicylhydroxamic acid, SHAM) alternative pathway is located in the inner membrane of plant mitochondria and electron flow through it is not coupled to H+ pumping and ATP synthesis. When estimating the activity and capacity of the alternative pathway in intact plant tissues three main problems arise: 1) There is almost always a substantial (10–50%) KCN-insensitive, SHAM-insensitive residual respiration, which may be due to peroxisomal a-oxidation of fatty acids, and which must be subtracted from all data in the further analyses. 2) There is a (KCN-sensitive) peroxidase in many tissues that is stimulated by low SHAM concentrations (1–10 mAf), but inhibited at higher concentrations (15–50 mM). 3) High concentrations of SHAM may inhibit the cytochrome pathway. Means of identifying and alleviating these problems are presented. Provided experimental conditions are chosen such as to minimize the three problems for each new plant organ or species or each new growth condition, SHAM can be used to estimate the size of the alternatively pathway in vivo.