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.
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References
Amthor JS (1989) Respiration and crop productivity. Plant Growth Regul 10:271–273
Amthor JS (2000) The McCree-de Wit-Penning de Vries-Thornley respiration paradigms: 30 years later. Ann Bot 86:1–20
Aschan G, Pfanz H (2003) Non-foliar photosynthesis—a stratey of additional carbon acquisition. Flora 198:81–97
Baryeh EA (2001) Physical properties of bambara groundnuts. J Food Eng 47:321–326
Bazzaz F, Carlson R (1979) Photosynthetic contribution of flowers and seeds to reproductive effort of an annual colonizer. New Phytol 82:223–232
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
Blanke MM, Notton BA (1991) Kinetics and physiological significance of photosynthetic phosphoenolpyruvate carboxylase in avocado fruit. J Plant Physiol 137(5):553–558
Blanke MM, Whiley AW (1995) Bioenergetics, respiration cost and water relations of developing avocado fruit. J Plant Physiol 145(s1–2):87–92
Blanke MM, Notton BA, Hucklesby DP (1986) Physical and kinetic properties of photosynthetic phosphoenolpyruvate carboxylase in developing apple fruit. Phytochemistry 25(3):601–606
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
Charles-Edwards DA (1981) The mathematics of photosynthesis and productivity. Academic Press, London
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
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
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
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
Huang J, Lv FD, He XH (2011) Preliminary study of photosynthesis in Carya illinoensis. J Cent South Univ For Technol 31:174–177
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
Jindal VK, Mohsenin NN (1978) Dynamic hardness determination of corn kernels from impact tests. J Agr Eng Res 23(1):77–84
Kocurek M, Kornas A, Pilarski J, Tokarz K (2015) Photosynthetic activity of stems in two Clusia species. Trees 29:1029–1040
Koyama K, Kikuzawa K (2010) Geometrical similarity analysis of photosynthetic light response curves, light saturation and light use efficiency. Oecologia 164:53–63
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
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
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
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
Ling H et al (2014) Comparison of leaf photosynthetic physiological characteristics in five Carya illinoensis varieties. Scientia Silvae Sinicae 50:174–178
Lloyd J et al (1995) Measuring and modelling whole-tree gas exchange. Funct Plant Biol 22:987–1000
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
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
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
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
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
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
Racker E (1962) Ribulose diphosphate carboxylase from spinach leaves: ribulose diphosphate + CO2 + H2O → 2 3-P-Glycerate. Method Enzymol 5:266–270
Ranjan S, Singh R, Soni DK, Pathre UV, Shirke PA (2012) Photosynthetic performance of Jotropha curcas fruits. Plant Physiol Biochem 52:66–76
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
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
Warren CR, Adams MA (2002) Phosphorus affects growth and partitioning of nitrogen to Rubisco in Pinus pinaster. Tree Physiol 22:11–19
Warren CR, Adams MA (2004) Evergreen trees do not maximize instantaneous photosynthesis. Trends Plant Sci 9:270–274
Weiss D, Schönfeld M, Halevy AH (1988) Photosynthetic activities in the Petunia corolla. Plant Physiol 87:666–670
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
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).
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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
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DOI: https://doi.org/10.1007/s00468-016-1386-5