Summary• High-temperature, low-light (HTLL) treatment of 35S:PAP1 Arabidopsis thaliana over-expressing the PAP1 (Production of Anthocyanin Pigment 1) gene results in reversible reduction of red colouration, suggesting the action of additional anthocyanin regulators. High-performance liquid chromatography (HPLC), liquid chromatography mass spectrometry (LCMS) and Affimetrix ® -based microarrays were used to measure changes in anthocyanin, flavonoids, and gene expression in response to HTLL.• HTLL treatment of control and 35S:PAP1 A. thaliana resulted in a reversible reduction in the concentrations of major anthocyanins despite ongoing over-expression of the PAP1 MYB transcription factor. Twenty-one anthocyanins including eight ciscoumaryl esters were identified by LCMS. The concentrations of nine anthocyanins were reduced and those of three were increased, consistent with a sequential process of anthocyanin degradation. Analysis of gene expression showed down-regulation of flavonol and anthocyanin biosynthesis and of transport-related genes within 24 h of HTLL treatment. No catabolic genes up-regulated by HTLL were found.• Reductions in the concentrations of anthocyanins and down-regulation of the genes of anthocyanin biosynthesis were achieved by environmental manipulation, despite ongoing over-expression of PAP1. Quantitative PCR showed reduced expression of three genes (TT8, TTG1 and EGL3) of the PAP1 transcriptional complex, and increased expression of the potential transcriptional repressors AtMYB3, AtMYB6 and AtMYBL2 coincided with HTLL-induced down-regulation of anthocyanin biosynthesis.• HTLL treatment offers a model system with which to explore anthocyanin catabolism and to discover novel genes involved in the environmental control of anthocyanins.
Effects of elevated root zone (RZ) CO2 and air temperature on photosynthesis, productivity, nitrate (NO3–), and total reduced nitrogen (N) content in aeroponically grown lettuce plants were studied. Three weeks after transplanting, four different RZ [CO2] concentrations [ambient (360 ppm) and elevated concentrations of 2000, 10 000, and 50 000 ppm] were imposed on plants grown at two air temperature regimes of 28 °C/22 °C (day/night) and 36 °C/30 °C. Photosynthetic CO2 assimilation (A) and stomatal conductance (gs) increased with increasing photosynthetically active radiation (PAR). When grown at 28 °C/22 °C, all plants accumulated more biomass than at 36 °C/30 °C. When measured under a PAR ≥600 μmol m−2 s−1, elevated RZ [CO2] resulted in significantly higher A, lower gs, and higher midday leaf relative water content in all plants. Under elevated RZ [CO2], the increase of biomass was greater in roots than in shoots, causing a lower shoot/root ratio. The percentage increase in growth under elevated RZ [CO2] was greater at 36 °C/30 °C although the total biomass was higher at 28 °C/22 °C. NO3– and total reduced N concentrations of shoot and root were significantly higher in all plants under elevated RZ [CO2] than under ambient RZ [CO2] of 360 ppm at both temperature regimes. At each RZ [CO2], NO3– and total reduced N concentration of shoots were greater at 28 °C/22 °C than at 36 °C/30 °C. At all RZ [CO2], roots of plants at 36 °C/30 °C had significantly higher NO3– and total reduced N concentrations than at 28 °C/22 °C. Since increased RZ [CO2] caused partial stomatal closure, maximal A and maximal gs were negatively correlated, with a unique relationship for each air temperature. However, across all RZ [CO2] and temperature treatments, there was a close correlation between maximal A and total shoot reduced N concentration of plants under different RZ [CO2], indicating that increased A under elevated RZ [CO2] could partially be due to the higher shoot total reduced N.
A compartmental growth model was developed to describe expansion of ' Delicious ' apple fruit diameter and the effect of early-season temperatures on potential size at harvest. The model was based on the assumption that growth may be described as a function of transfer between two conceptual compartments. Under this scheme, the first compartment represented all tissue contributing to the setting of potential fruit size (determined as the integral of its output) whereas the second compartment represented all other fruit tissue whose growth actualized that potential. Expansion of both compartments was assumed to have a temperature response with an optimum, whereas an aging process with an asymptotic temperature response controlled transfer to the second compartment. Model parameters were estimated by fitting to data from controlled environment experiments in which early-season temperature conditions were varied. Predicted fruit growth curves showed close agreement with measured diameter data. The results were consistent with a two-fold impact of early-season temperatures on apple fruit size : an immediate, direct effect on growth rate and an enduring effect, mediated through fruit cell number or resource allocation to young fruit, reflecting the establishment of a potential that subsequent growth actualizes. # 1999 Annals of Botany Company
Patterns of shoot development and the production of different types of shoots were compared with scion leaf area index (LAI) to identify how eight clonal Actinidia rootstocks influence scion development. Rootstocks selected from seven Actinidia species (A. chrysantha Merri., A. deliciosa (A. Chev.) C. F. Liang et A.R. Ferguson, A. eriantha Benth., A. hemsleyana Dunn, A. kolomikta (Maxim. et Rupr.) Maxim., A. kolomikta C.F. Liang and A. polygama (Sieb. et Zucc.) Maxim.) were grafted with the scion Actinidia chinensis Planch. var. chinensis 'Hort16A' (yellow kiwifruit). Based on an earlier architectural analysis of A. chinensis, axillary shoot types produced by the scion were classified as short, medium or long. Short and medium shoots produced a restricted number of preformed leaves before the shoot apex ceased growth and aborted, resulting in a 'terminated' shoot. The apex of long shoots continued growth and produced more nodes throughout the growing seasons. Mid-season LAI of the scion was related to the proportion of shoots that ceased growth early in the season. Scions on low-vigor rootstocks had 50% or less leaf area than scions on the most vigorous rootstocks and had a higher proportion of short and medium shoots. On low-vigor rootstocks, a higher proportion of short shoots was retained during pruning to form the parent structure of the following year. Short parent shoots produced a higher proportion of short daughter shoots than long parent shoots, thus reinforcing the effect of the low-vigor rootstocks. However, overall effects of rootstock on shoot development were consistent regardless of parent shoot type and nodal position within the parent shoot. Slower-growing shoots were more likely to terminate and scions on low-vigor rootstocks produced a higher proportion of slow-growing shoots. Shoot termination also occurred earlier on low-vigor rootstocks. The slower growth of terminating shoots was detectable from about 20 days after bud burst. Removal of a proportion of shoots at the end of bud burst increased the growth rate and decreased the frequency of termination of the remaining shoots on all rootstocks, indicating that the fate of a shoot was linked to competitive interactions among shoots during initial growth immediately after bud burst. Rootstock influenced the process of shoot termination independently of its effect on final leaf size. Scions on low-vigor rootstocks had a higher proportion of short shoots and short shoots on all rootstocks had smaller final leaf sizes at equivalent nodes than medium or long shoots. Only later in the development of long shoots was final leaf size directly related to rootstock, with smaller leaves on low-vigor rootstocks. Thus, the most important effect of these Actinidia rootstocks on scion development occurred during the initial period of shoot growth immediately after bud burst.
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