Abstract

Supplementary lighting is frequently applied in the winter season for crop production in greenhouses. The effect of supplementary lighting on plant growth depends on the balance between assimilate production in source leaves and the overall capacity of the plants to use assimilates. This study aims at quantifying the source–sink balance and carbohydrate content of three tomato cultivars differing in fruit size, and to investigate to what extent the source/sink ratio correlates with the potential fruit size. Cultivars Komeet (large size), Capricia (medium size), and Sunstream (small size, cherry tomato) were grown from 16 August to 21 November, at similar crop management as in commercial practice. Supplementary lighting (High Pressure Sodium lamps, photosynthetic active radiation at 1 m below lamps was 162 μmol photons m-2 s-1; maximum 10 h per day depending on solar irradiance level) was applied from 19 September onward. Source strength was estimated from total plant growth rate using periodic destructive plant harvests in combination with the crop growth model TOMSIM. Sink strength was estimated from potential fruit growth rate which was determined from non-destructively measuring the fruit growth rate at non-limiting assimilate supply, growing only one fruit on each truss. Carbohydrate content in leaves and stems were periodically determined. During the early growth stage, ‘Komeet’ and ‘Capricia’ showed sink limitation and ‘Sunstream’ was close to sink limitation. During this stage reproductive organs had hardly formed or were still small and natural irradiance was high (early September) compared to winter months. Subsequently, during the fully fruiting stage all three cultivars were strongly source-limited as indicated by the low source/sink ratio (average source/sink ratio from 50 days after planting onward was 0.17, 0.22, and 0.33 for ‘Komeet,’ ‘Capricia,’ and ‘Sunstream,’ respectively). This was further confirmed by the fact that pruning half of the fruits hardly influenced net leaf photosynthesis rates. Carbohydrate content in leaves and stems increased linearly with the source/sink ratio. We conclude that during the early growth stage under high irradiance, tomato plants are sink-limited and that the level of sink limitation differs between cultivars but it is not correlated with their potential fruit size. During the fully fruiting stage tomato plants are source-limited and the extent of source limitation of a cultivar is positively correlated with its potential fruit size.

Highlights

  • Plant growth is closely correlated with source and sink strength and the balance between them (Gifford and Evans, 1981; Wardlaw, 1990; Smith and Stitt, 2007)

  • Plant Growth Maximum growth rate and growth duration of single fruit were highest in ‘Komeet’; while these parameters were lowest in ‘Sunstream’ (Figure 2). These differences together resulted in the largest potential fruit size in ‘Komeet’ and smallest in ‘Sunstream.’ Potential fresh fruit weight was 180 g for ‘Komeet,’ 137 g for ‘Capricia,’ and 20 g for ‘Sunstream’ as determined in this study

  • Carbohydrate Content and Net Photosynthesis Rate In tomato stems, starch content was negligible compared to sugar content which was apparently the main carbohydrate in stems (Figures 4A,B)

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Summary

Introduction

Plant growth is closely correlated with source and sink strength and the balance between them (Gifford and Evans, 1981; Wardlaw, 1990; Smith and Stitt, 2007). Source strength of a plant is defined as the rate at which the plant produces assimilates (photosynthesis rate). The sink strength of a plant is composed of sink strengths of all individual organs. Sink strength of an organ is the competitive ability of an organ to attract assimilates and can be quantified by its potential growth rate (Marcelis, 1996). Fruits are the major sink organs in crops like tomato, leaves, stems, and roots utilize assimilates and have a sink strength; leaves are source organ and sink organ Limited sink demand could result in feedback regulation of photosynthesis as it may down-regulate the net photosynthetic activity through carbohydrate accumulation in source leaves (Iglesias et al, 2002; Franck et al, 2006; McCormick et al, 2006; Velez-Ramirez et al, 2014)

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