Skip to main content
Log in

Photosynthetic characteristics of leaves and fruits of Hickory (Carya cathayensis Sarg.) and Pecan (Carya illinoensis K.Koch) during fruit development stages

  • Original Article
  • Published:
Trees Aims and scope Submit manuscript

Abstract

Key message

Fruit photosynthesis in both hickory and pecan significantly contribute to the carbon requirements of late growth stage (corresponding to seed development).

Abstract

Plant parts other than leaves can perform photosynthesis and contribute to carbon acquisition for fruit development. To determine the role of fruit photosynthesis in fruit carbon acquisition in hickory (Carya cathayensis Sarg.) and pecan (Carya illinoensis K.Koch), we studied changes in dry mass, surface area and CO2 exchange rate in these fruits during fruit development. Fruit development was divided into two phases: phase one involves the rapid increase of fruit size (from 0 to 59 days after pollination (DAP) for hickory; from 0 to 88 DAP for pecan); phase two involves seed development (from 59 to 121 DAP for hickory; from 88 to 155 DAP for pecan). The net photosynthetic rate (P n) in hickory leaves decreased by 48.5 % from 76 to 88 DAP, while the P n in pecan leaves decreased by 32.3 % from 88 to 123 DAP. The gross photosynthetic rate (P g) in hickory fruit was significantly greater than that of the leaf during the late stage (88 to 121 DAP) of fruit development. Pecan fruit had a significantly higher P g than leaves during ontogeny. The contribution of fruit photosynthesis to fruit carbon requirements increased during fruit development, which was estimated by the gross fruit photosynthesis divided by respiration and increased dry mass. The contribution of fruit photosynthesis to pecan carbon requirements was significantly greater than that of hickory. Fruit photosynthesis in both hickory and pecan significantly contribute to the carbon requirements of late growth stage.

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.

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

Similar content being viewed by others

References

  • Amthor JS (1989) Respiration and crop productivity. Plant Growth Regul 10:271–273

    Google Scholar 

  • Amthor JS (2000) The McCree-de Wit-Penning de Vries-Thornley respiration paradigms: 30 years later. Ann Bot 86:1–20

    Article  CAS  Google Scholar 

  • Aschan G, Pfanz H (2003) Non-foliar photosynthesis—a stratey of additional carbon acquisition. Flora 198:81–97

    Article  Google Scholar 

  • Baryeh EA (2001) Physical properties of bambara groundnuts. J Food Eng 47:321–326

    Article  Google Scholar 

  • Bazzaz F, Carlson R (1979) Photosynthetic contribution of flowers and seeds to reproductive effort of an annual colonizer. New Phytol 82:223–232

    Article  Google Scholar 

  • Biscoe P, Scott R, Monteith J (1975) Barley and its environment. III. Carbon budget of the stand. J Appl Ecol, pp 269–293

  • Blanke MM, Lenz F (1989) Fruit photosynthesis. Plant Cell Environ 12:31–46

    Article  CAS  Google Scholar 

  • Blanke MM, Notton BA (1991) Kinetics and physiological significance of photosynthetic phosphoenolpyruvate carboxylase in avocado fruit. J Plant Physiol 137(5):553–558

    Article  CAS  Google Scholar 

  • Blanke MM, Whiley AW (1995) Bioenergetics, respiration cost and water relations of developing avocado fruit. J Plant Physiol 145(s1–2):87–92

    Article  CAS  Google Scholar 

  • Blanke MM, Notton BA, Hucklesby DP (1986) Physical and kinetic properties of photosynthetic phosphoenolpyruvate carboxylase in developing apple fruit. Phytochemistry 25(3):601–606

    Article  CAS  Google Scholar 

  • Blanke MM, Hucklesby DP, Notton BA (1987) Distribution and physiological significance of photosynthetic phosphoenolpyruvate carboxylase in developing apple fruit. J Plant Physiol 129(s3–4):319–325

    Article  CAS  Google Scholar 

  • Charles-Edwards DA (1981) The mathematics of photosynthesis and productivity. Academic Press, London

    Google Scholar 

  • Crews C, Worley R, Syvertsen J, Bausher M (1980) Carboxylase activity and seasonal changes in CO2 assimilation rates in three cultivars of pecan. J Am Soc Hortic Sci 105:798–801

    CAS  Google Scholar 

  • Diver SG, Smith MW, McNew RW (1984) Influence of fruit development on seasonal elemental concentrations and distribution in fruit and leaves of pecan. Commun Soil Sci Plant 15:619–637

    Article  CAS  Google Scholar 

  • Hieke S, Menzel C, Lüdders P (2002) Effects of leaf, shoot and fruit development on photosynthesis of lychee trees (Litchi chinensis). Tree Physiol 22:955–961

    Article  CAS  PubMed  Google Scholar 

  • Hu YY, Oguchi R, Yamori W, von Caemmerer S, Chow WS, Zhang WF (2013) Cotton bracts are adapted to a microenvironment of concentrated CO2 produced by rapid fruit respiration. Ann Bot-London 112:31–40

    Article  Google Scholar 

  • Huang J, Lv FD, He XH (2011) Preliminary study of photosynthesis in Carya illinoensis. J Cent South Univ For Technol 31:174–177

    Google Scholar 

  • Imai S, Ogawa K (2009) Quantitative analysis of carbon balance in the reproductive organs and leaves of Cinnamomum camphora (L.) Presl. J Plant Res 122:429–437

    Article  CAS  PubMed  Google Scholar 

  • Jindal VK, Mohsenin NN (1978) Dynamic hardness determination of corn kernels from impact tests. J Agr Eng Res 23(1):77–84

    Article  Google Scholar 

  • Kocurek M, Kornas A, Pilarski J, Tokarz K (2015) Photosynthetic activity of stems in two Clusia species. Trees 29:1029–1040

    Article  CAS  Google Scholar 

  • Koyama K, Kikuzawa K (2010) Geometrical similarity analysis of photosynthetic light response curves, light saturation and light use efficiency. Oecologia 164:53–63

    Article  PubMed  Google Scholar 

  • Kura-Hotta M, Satoh K, Katoh S (1987) Relationship between photosynthesis and chlorophyll content during leaf senescence of rice seedlings. Plant Cell Physiol 28:1321–1329

    CAS  Google Scholar 

  • Lawlor DW, Kontturi M, Young AT (1989) Photosynthesis by flag leaves of wheat in relation to protein, ribulose bisphosphate carboxylase activity and nitrogen supply. J Exp Bot 40:43–52

    Article  CAS  Google Scholar 

  • Li BH, Chi DB, Cheng HH, Li ZL (2007) Relationship between photosynthetic characteris and yield of the Carya cathyensis Sarg. China For Sci Technol 21:34–37

    Google Scholar 

  • Lichtenthaler HK (1987) Chlorophylls and carotenoids: Pigments of photosynthetic biomembranes. Methods Enzymol, pp 350–382

  • Linder S, Troeng E (1981) The seasonal course of respiration and photosynthesis in strobili of scots pine. For Sci 27:267–276

    Google Scholar 

  • Ling H et al (2014) Comparison of leaf photosynthetic physiological characteristics in five Carya illinoensis varieties. Scientia Silvae Sinicae 50:174–178

    CAS  Google Scholar 

  • Lloyd J et al (1995) Measuring and modelling whole-tree gas exchange. Funct Plant Biol 22:987–1000

    Google Scholar 

  • Lombardini L, Restrepo-Diaz H, Volder A (2009) Photosynthetic light response and epidermal characteristics of sun and shade pecan leaves. J Am Soc Hortic Sci 134:372–378

    Google Scholar 

  • Lytovchenko A, Eickmeier I, Pons C, Osorio S, Szecowka M, Lihmberg K, Lu YH, Fisahn J, Bock R, Stitt M, Grimm B, Granell A, Fernie AR (2011) Tomato fruit photosynthesis is seemingly unimportant in primary metabolism and ripening but plays a considerable role in seed development. Plant Physiol 157:1650–1663

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Makino A, Mae T, Ohira K (1983) Photosynthesis and ribulose-1,5-bisphosphate in rice leaves: changes in photosynthesis and enzymes involved in carbon assimilation from leaf development through senescence. Plant Physiol 73(4):1002–1007

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Marcelis LFM, Hofman-Eijer LRB (1995) The contribution of fruit photosynthesis to the carbon requirement of cucumber fruits as affected by irradiance, temperature and ontogeny. Physiol Plant 93:476–483

    Article  CAS  Google Scholar 

  • Ogawa K, Furukawa A, Hagihara A, Abdullah AM, Awang M (1995) In situ CO2 gas-exchange in fruits of a tropical tree Durio zibethinus Murray. Trees 9:241–246

    Article  Google Scholar 

  • Pavel E, DeJong TM (1993) Estimating the photosynthetic contribution of developing peach (Prunus persica) fruits to their growth and maintenance carbohydrate requirements. Physiol Plant 88:331–338

    Article  CAS  Google Scholar 

  • Racker E (1962) Ribulose diphosphate carboxylase from spinach leaves: ribulose diphosphate + CO2 + H2O → 2 3-P-Glycerate. Method Enzymol 5:266–270

    Article  CAS  Google Scholar 

  • Ranjan S, Singh R, Soni DK, Pathre UV, Shirke PA (2012) Photosynthetic performance of Jotropha curcas fruits. Plant Physiol Biochem 52:66–76

    Article  CAS  PubMed  Google Scholar 

  • Read SM, Northcote DH (1981) Minimization of variation in the response to different protein of the Coomassic Blue G dye binding assay for protein. Anal Biochem 116:53–64

    Article  CAS  PubMed  Google Scholar 

  • Sayre RT, Kennedy RA, Pringnitz DJ (1979) Photosynthetic enzyme activities and localization in Mollugo verticillata populations differing in the levels of C3 and C4 cycle operation. Plant Physiol 64:293–299

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Warren CR, Adams MA (2002) Phosphorus affects growth and partitioning of nitrogen to Rubisco in Pinus pinaster. Tree Physiol 22:11–19

    Article  CAS  PubMed  Google Scholar 

  • Warren CR, Adams MA (2004) Evergreen trees do not maximize instantaneous photosynthesis. Trends Plant Sci 9:270–274

    Article  CAS  PubMed  Google Scholar 

  • Weiss D, Schönfeld M, Halevy AH (1988) Photosynthetic activities in the Petunia corolla. Plant Physiol 87:666–670

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Xie HE, Huang YJ, Xue XM, Xu CS, Liu L (2008) Growth and development of the Carya cathayensis nut. J Zhejiang A & F Univ 4:527–531

    Google Scholar 

Download references

Acknowledgments

This work was supported by a Grant from the Zhejiang Provincial Natural Science Foundation of China (LY15C160003), the National High Technology Research and Development Program of China (863 Program) (2013AA102605), the Zhejiang Provincial Science, Technology Innovation Activity for College Students (2015R412044), and National Natural Science Foundation of China (31100229, 31470682).

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Yuanyuan Hu.

Ethics declarations

Conflict of interest

The authors declare that they have no conflict of interest.

Additional information

Communicated by D. Treutter.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Xu, Q., Wu, J., Cao, Y. et al. Photosynthetic characteristics of leaves and fruits of Hickory (Carya cathayensis Sarg.) and Pecan (Carya illinoensis K.Koch) during fruit development stages. Trees 30, 1523–1534 (2016). https://doi.org/10.1007/s00468-016-1386-5

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00468-016-1386-5

Keywords

Navigation