Skip to main content
Log in

Differential source–sink manipulation affects leaf carbohydrate and photosynthesis of early- and late-harvest nectarine varieties

  • Published:
Theoretical and Experimental Plant Physiology Aims and scope Submit manuscript

Abstract

Source–sink balance is a major determinant of carbon partitioning within plants. Thinning is an agronomic practice that consists of changing the ratio between leaves and fruits, the source and sink plant organs, respectively. Decreasing the fruit load on a peach tree is supposed to lead to an increase in fruit size and sometimes in soluble solid content in the remaining fruit. However, this response would change in early and late harvest peach varieties when considering the reduction in sink organs and decrease in photosynthetic process. The aim of this work was to study the effects of source–sink balance on physiological and metabolic parameters of two nectarine varieties with different fruit time development and harvest. Differential thinning was concurrently performed in trees of both varieties. Fruit development kinetics in addition to physiological parameters, such as chlorophyll fluorescence, gas-exchange, and leaf sugar composition, were determined over two harvest seasons. The decrease in photosynthetic rate in thinned trees was associated with stomata limitation and transitory sugar accumulation in leaves with sorbitol as the most abundant sugar. On the other hand, most photochemical processes remained constant in leaves of both varieties regardless of the thinning treatment. We suggest that increasing the source–sink ratio via thinning treatment leads to transient soluble sugar accumulation in the leaves and indicates an imbalance in drain capacity resulting in reduced photosynthesis and stomatal closure. In these nectarine varieties, thinning led to lower net photosynthesis but had no significant impact on final fruit size. Fruit thinning also allowed the development of other sink organs (such as vegetative suckers) and probably occurred as an acclimation process in order to maintain source–sink balance within the tree.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Institutional subscriptions

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5
Fig. 6
Fig. 7
Fig. 8

Similar content being viewed by others

References

  • Baker NR (2008) Chlorophyll fluorescence: a probe of photosynthesis in vivo. Annu Rev Plant Biol 59:89–113

    Article  CAS  PubMed  Google Scholar 

  • Berman ME, DeJong TM (1996) Water stress and crop load effects on fruit fresh and dry weights in peach (Prunus persica). Tree Physiol 16:859–864

    Article  CAS  PubMed  Google Scholar 

  • Bickford R, Hennicke L (2013) Chile stone fruits annual fresh peaches, nectarines and cherries annual. GAIN report number: CI1313

  • Björkman O, Demmig B (1987) Photon yield of O2 evolution and chlorophyll fluorescence characteristics at 77 K among vascular plants of diverse origins. Planta 170:489–504

    Article  PubMed  Google Scholar 

  • Bustan A, Dag A, Yermiyahu U, Erel R, Presnov E, Agam N, Kool D, Iwema J, Zipori I, Ben-Gal A (2016) Fruit load governs transpiration of olive trees. Tree Physiol. https://doi.org/10.1093/treephys/tpv138

    Article  PubMed  PubMed Central  Google Scholar 

  • Cheng J, Fan P, Liang Z, Wang Y, Niu N, Li W, Li S (2009) Accumulation of end products in source leaves affects photosynthetic rate in peach via alteration of stomatal conductance and photosynthetic efficiency. J Am Soc Hortic Sci 134(6):667–676

    Article  Google Scholar 

  • Coneva ED, Cline JA (2006) Blossom thinners reduce crop load and increase fruit size and quality of peaches. Hortic Sci 41(5):1253–1258

    CAS  Google Scholar 

  • DaMatta FM, Cuncha RL, Antunes WC, Martins SCV, Araujo WL, Fernie AR, Moraes GAB (2008) In field-grown coffee trees source-sink manipulation alters photosynthetic rates, independently of carbon metabolism, via alterations in stomatal function. New Phytol 178(2):348–357

    Article  CAS  PubMed  Google Scholar 

  • Dean JFD (1997) Lignin analysis. In: Dashek WV (ed) Methods in plant biochemistry and molecular biology. CRC Press, Boca Ratón, pp 199–215

    Google Scholar 

  • DeJong TM (1986) Fruit effects on photosynthesis in Prunus persica. Physiol Plant 66:149–153

    Article  Google Scholar 

  • Dejong TM, Grossman YL (1995) Quantifying sink and source limitations on dry matter partitioning to fruit growth in peach trees. Physiol Plant 95(3):437–443

    Article  CAS  Google Scholar 

  • Demmig-Adams B, Cohu CM, Muller O, Adams WW (2012) Modulation of photosynthetic energy conversion efficiency in nature: from seconds to seasons. Photosynth Res 113(1–3):75–88

    Article  CAS  PubMed  Google Scholar 

  • Duan W, Fan PG, Wang LJ, Li WD, Yan ST, Li SH (2008) Photosynthetic response to low sink demand after fruit removal in relation to photoinhibition and photoprotection in peach trees. Tree Physiol 28(1):123–132

    Article  CAS  PubMed  Google Scholar 

  • Franck N, Vaast P, Génard M, Dauzat J (2006) Soluble sugars mediate sink feedback down-regulation of leaf photosynthesis in field-grown Coffea arabica. Tree Physiol 26(4):517–525

    Article  CAS  PubMed  Google Scholar 

  • Gucci R, Grappadelli LC, Tustin S, Ravaglia G (1995) The effect of defruiting at different stages of fruit development on leaf photosynthesis of ‘Golden Delicious’ apple. Tree Physiol 15:35–40

    Article  CAS  PubMed  Google Scholar 

  • Guidi L, Lo Piccolo E, Landi M (2019) Chlorophyll fluorescence, photoinhibition and abiotic stress: does it make any difference the fact to be a C3 or C4 species? Front Plant Sci 10:174

    Article  PubMed  PubMed Central  Google Scholar 

  • Huang H, Cheng Z, Zhang Z, Wang Y (2008) History of cultivation and trends in China. In: Layne DR, Bassi D (eds) The peach: botany, production and uses. CAB International Press, Wallingford, pp 37–60

    Chapter  Google Scholar 

  • Iglesias DJ, Lliso I, Tadeo FR, Talon M (2002) Regulation of photosynthesis through source:sink imbalance in citrus is mediated by carbohydrate content in leaves. Physiol Plant 116:563–572

    Article  CAS  Google Scholar 

  • Klughammer C, Schreiber U (2008) Complementary PS II quantum yields calculated from simple fluorescence parameters measured by PAM fluorometry and the Saturation Pulse method. PAM Appl Notes 1:27–35

    Google Scholar 

  • Li WD, Li SH, Yang SH, Yang JM, Zheng XB, Li XD, Yao HM (2005) Photosynthesis in response to sink–source manipulation during different phenological stages of fruit development in peach trees: regulation by stomatal aperture and leaf temperature. J Hortic Sci Biotechnol 80:481–487

    Article  Google Scholar 

  • Li WD, Duan W, Fan PG, Yan ST, Li SH (2007) Photosynthesis in response to sink-source activity and in relation to end products and activities of metabolic enzymes in peach trees. Tree Physiol 27(9):1307–1318

    Article  CAS  PubMed  Google Scholar 

  • Matsuda R, Suzuki K, Nakano A, Higashide T, Takaichi M (2011) Responses of leaf photosynthesis and plant growth to altered source–sink balance in a Japanese and a Dutch tomato cultivar. Sci Hortic 127:520–527

    Article  Google Scholar 

  • McFadyen LM, Hutton RJ, Barlow EWR (1996) Effects of crop load in fruit water relations and fruit growth in peach. J Hortic Sci 71:469–480

    Article  Google Scholar 

  • Minchin PEH, Thorpe MR (1987) Is phloem transport due to a hydrostatic pressure gradient? Supporting evidence from pressure chamber experiments. Aust J Plant Physiol 14:397–402

    Google Scholar 

  • Minchin PEH, Thorpe MR, Hall JL, Baker DA, Oparka KL (1996) What determines carbon partitioning between competing sinks? J Exp Bot 47:1293–1296

    Article  CAS  PubMed  Google Scholar 

  • Moing A, Carbonne F, Rashad MH, Gaudillère J (1992) Carbon fluxes in mature peach leaves. Plant Physiol 100(4):1878–1884

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Moing A, Maucourt M, Renaud C, Guadillère M, Brouquisse R, Lebouteiller B, Gousset-Dupont A, Vidal J, Granot D, Denoyes-Rothan B, Lerceteau-Köhler E, Rolin D (2004) Quantitative metabolic profiling by 1-dimensional 1H-NMR analyses: application to plant genetics and functional genomics. Funct Plant Biol 31(9):889–902

    Article  CAS  Google Scholar 

  • Morandi B, Rieger M, Grappadelli LC (2007) Vascular flows and transpiration affect peach (Prunus persica Batsch.) fruit daily growth. J Exp Bot 58(14):3941–3947

    Article  CAS  PubMed  Google Scholar 

  • Nebauer SG, Renau-Morata B, Guardiola JL, Molina R (2011) Photosynthesis down-regulation precedes carbohydrate accumulation under sink limitation in Citrus. Tree Physiol 31:169–177

    Article  CAS  PubMed  Google Scholar 

  • Ognjanov V, Vujanic-Varga D, Misic PD, Veresbaranji I, Macet K, Tsovic Z, Petrovic N (1995) Anatomical and biochemical studies of fruit development in peach. Sci Hortic 64:33–48

    Article  Google Scholar 

  • Paul MJ, Foyer CH (2001) Sink regulation of photosynthesis. J Exp Bot 52:1383–1400

    Article  CAS  PubMed  Google Scholar 

  • Pavel E, DeJong T (1993) Source- and sink-limited growth periods of developing peach fruits indicated by relative growth rate analysis. J Am Soc Hortic Sci 118(6):820–824

    Article  Google Scholar 

  • Ribeiro RV, Machado EC, Habermann G, Santos MG, Oliveira RF (2012) Seasonal effects on the relationship between photosynthesis and leaf carbohydrate in orange trees. Funct Plant Biol 39:471–480

    Article  CAS  Google Scholar 

  • Rivas F, Gravina A, Augustí M (2007) Girdling effects on fruit set and quantum yield efficiency of PSII in two citrus cultivars. Tree Physiol 27:527–535

    Article  CAS  PubMed  Google Scholar 

  • Urban L, Léchaudel M, Lu P (2004) Effect of fruit load and girdling on leaf photosynthesis in Mangifera indica L. J Exp Bot 55:2075–2085

    Article  CAS  PubMed  Google Scholar 

  • Volpe G, Lo Bianco R, Rieger M (2008) Carbon autonomy of peach shoots determined by 13C-photoassimilate transport. Tree Physiol 28:1805–1812

    Article  CAS  PubMed  Google Scholar 

  • Wang H, Wang F, Wang G, Majourhat K (2007) The responses of photosynthetic capacity, chlorophyll fluorescence and chlorophyll content of nectarine (Prunus persica var. Nectarina Maxim) to greenhouse and field grown conditions. Sci Hortic 112(1):66–72

    Article  CAS  Google Scholar 

  • Wellburn AR (1994) The spectral determination of chlorophylls a and b, as well as total carotenoids, using various solvents with spectrophotometers of different resolution. Plant Physiol 144:307–313

    Article  CAS  Google Scholar 

  • Westwood MN (1993) Fruit growth and thinning. In: Westwood MN (ed) Temperate-zone pomology. Timber Press Portland, Oregon, pp 254–274

    Google Scholar 

  • Wu BH, Ben MM, Génard M, Lescourret F, Besset J, Bussi C (2005) Peach fruit growth in relation to the leaf-to-fruit ratio, early fruit size and fruit position. J Hortic Sci Biotechnol 80(3):340–345

    Article  Google Scholar 

  • Wu BH, Huang HQ, Fan PG, Li SH, Liu GJ (2008) Photosynthetic responses to sink–source manipulation in five peach cultivars varying in maturity date. J Am Soc Hortic Sci 133(2):278–283

    Article  Google Scholar 

  • Yan ST, Li XD, Li WD, Fan PG, Duan W, Li SH (2011) Photosynthesis and chlorophyll fluorescence response to low sink demand of tubers and roots in Dahlia pinnata source leaves. Biol Plant 55(1):83–89

    Article  CAS  Google Scholar 

  • Zhang SR (1999) A discussion on chlorophyll fluorescence kinetics parameters and their significance. Chin Bull Bot 16:444–448

    Google Scholar 

  • Zhou L, Quebedeaux B (2003) Changes in photosynthesis and carbohydrate metabolism in mature apple leaves in response to whole plant source-sink manipulation. J Am Soc Hortic Sci 128:113–119

    Article  CAS  Google Scholar 

Download references

Acknowledgements

We thank El Tambo nursery for giving access to their ochards to perform our experiments. This research was funded by Fondo Nacional de Desarrollo Científico y Tecnológico (FONDECYT, Chile) Grant No 1130197.

Author information

Authors and Affiliations

Authors

Contributions

AMA and EGP conceived the study. DA conducted most of the experiments in the field and the analysis of the results. MPC and GB conducted the experiments in the field. MPC performed the HPLC analysis. All authors were involved in the analysis and discussion of the results. DA and AMA wrote the paper. MPC and EGP revised the paper. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Andrea Miyasaka Almeida.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Andrade, D., Covarrubias, M.P., Benedetto, G. et al. Differential source–sink manipulation affects leaf carbohydrate and photosynthesis of early- and late-harvest nectarine varieties. Theor. Exp. Plant Physiol. 31, 341–356 (2019). https://doi.org/10.1007/s40626-019-00150-0

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s40626-019-00150-0

Keywords

Navigation