Physiological responses of Salix rehderiana and Populus cathayana grafted seedlings to nitrogen deficiency
HAN Qing-quan1,2, SONG Hai-feng1,2, TANG Duo-teng1,2, ZHANG Sheng1*
1Key Laboratory of Mountain Surface Processes and Ecological Regulation, Institute of Mountain Hazards and Environment, Chinese Academy of Sciences and Ministry of Water Sources, Chengdu 610041, China 2University of Chinese Academy of Sciences, Beijing 100049, China
Morphological and physiological responses of Salix plants are different from Populus to nitrogen (N) deficiency. In this study, grafting technology was used in S. rehderiana and P. cathayana to investigate the graft compatibility of Salix and Populus, and whether grafting could improve the resistance to N deficiency in Salicaceae plants. The survival rate, growth, biomass accumulation and allocation, gas exchange parameters and non-structural carbohydrates (NSCs) were measured to evaluate the resistance to N deficiency among different grafting combinations. The results showed that the graft compatibility between S. rehderiana and P. cathayana was quite high. The survival rate was 74% and 96% in S/P (S. rehderiana was used as scions and P. cathayana as rootstocks) and P/S (P. cathayana was used as scions and S. rehderiana as rootstocks) combinations, respectively. N deficiency reduced the survival rate in all grafting combinations, which were 53.3% and 86.7% in S/P and P/S, respectively. The survival rate of S/P was lower than that of the other grafting combinations. Under control and N-deficient conditions, the height, basal diameter, biomass and net photosynthetic rate (Pn) of P/P and P/S combinations were higher than those of S/S and S/P combinations. N deficiency significantly reduced growth rate, biomass accumulation and Pn in all grafting combinations. The rate between root biomass and aboveground biomass of S. rehderiana rootstock combinations (S/S and P/S) was significantly higher than those of P. catha-yana rootstock combinations (P/P and S/P) under both control and N-deficient conditions. It indicated that more photosynthates might be allocated to belowground in S. rehderiana, while to aboveground in P. cathayana. The NSCs in roots of all grafting combinations were more sensitive to N deficiency than in stems and leaves. Except for the S/P combination, the starch, fructose, sucrose and total soluble sugar concentrations were significantly increased in roots in P/P, S/S and P/S combinations. Additionally, under N-deficient condition, the NSCs contents were significantly higher in P/P and P/S combinations than in S/S and S/P combinations.
韩清泉, 宋海凤, 唐铎腾, 张胜. 川滇柳与青杨属间嫁接幼苗对氮素缺乏的生理响应[J]. 应用生态学报, 2017, 28(12): 3833-3840.
HAN Qing-quan, SONG Hai-feng, TANG Duo-teng, ZHANG Sheng. Physiological responses of Salix rehderiana and Populus cathayana grafted seedlings to nitrogen deficiency. Chinese Journal of Applied Ecology, 2017, 28(12): 3833-3840.
Guo W (郭 炜), Hu N (胡 南), Li X-P (李小平), et al. Comparative analysis of the performance of different lysis buffers for measuring the ploidy level of Salicaceae species. Bulletin of Botanical Research (植物研究), 2016, 36(5): 782-789 (in Chinese)
[2]
Ding T-Y (丁托娅). Origin, divergence and geographi-cal, distribution of Salicaceae. Acta Botanica Yunnanica (云南植物研究), 1995, 17(3): 277-290 (in Chinese)
[3]
Tang G-M (唐桂梅), Jiang W-B (姜卫兵), Weng M-L (翁忙玲). Willow family and its application in landscaping. Chinese Agricultural Science Bulletin (中国农学通报), 2007, 23(3): 318-323 (in Chinese)
[4]
Zamora DS, Apostol KG, Wyatt GJ. Biomass production and potential ethanol yields of shrub willow hybrids and native willow accessions after a single 3-year harvest cycle on marginal lands in central Minnesota, USA. Agroforestry Systems, 2014, 88: 593-606
[5]
Körner C. Alpine Plant Life-Functional Plant Ecology of High Mountain Ecosystems. Berlin: Springer-Verlag, 2003
[6]
Marschner P. Marschners’s Mineral Nutrition of Higher Plants. 3nd Ed. Amsterdam: Elsevier, 2012
[7]
Boyce RL, Larson JR, Sanford RL. Phosphorus and nitrogen limitations to photosynthesis in Rocky Mountain bristlecone pine (Pinas aristata) in Colorado. Tree Physiology, 2006, 26: 1477-1486
[8]
Zhang S, Jiang H, Zhao HX, et al. Sexually different physiological responses of Populus cathayana to nitrogen and phosphorus deficiencies. Tree Physiology, 2014, 34: 343-354
[9]
Chen J, Dong TF, Duan BL, et al. Sexual competition and N supply interactively affect the dimorphism and competiveness of opposite sexes in Populus cathayana. Plant, Cell & Environment, 2015, 38: 1285-1298
[10]
Song MY, Yu L, Jiang YL, et al. Nitrogen-controlled intra- and interspecific competition between Populus purdomii and Salix rehderiana drive primary succession in the Gongga Mountain glacier retreat area. Tree Physiology, 2017, 3: 1-16
[11]
Pina A, Errea P. A review of new advances in mechanism of graft compatibility-incompatibility. Scientia Horticulturae, 2005, 106: 1-11
[12]
García-Sánchez F, Syvertsen JP, Gimeno V, et al. Responses to flooding and drought stress by two citrus rootstock seedlings with different water-use efficiency. Phy-siologia Plantarum, 2007, 130: 532-542
[13]
Han Y, Wang YH, Jiang H, et al. Reciprocal grafting separates the roles of the root and shoot in sex-related drought responses in Populus cathayana males and females. Plant, Cell & Environment, 2013, 36: 356-364
[14]
Poor RE. Investigating the effect of grafted watermelon on tolerance to drought and salinity. Journal of Novel Applied Sciences, 2015, 4: 670-673
[15]
Stegemann S, Bock R. Exchange of genetic material between cells in plant tissue grafts. Science, 2009, 324: 649-651
[16]
Gurdon G, Svab Z, Feng YP, et al. Cell-to-cell movement of mitochondria in plants. Proceedings of the National Academy of Sciences of the United States of America, 2016, 113: 3395-3400
[17]
Lewsey MG, Hardcastle TJ, Melnyk CW, et al. Mobile small RNAs regulate genome-wide DNA methylation. Proceedings of the National Academy of Sciences of the United States of America, 2016, 113: E801-E810
[18]
Fuentes I, Stegemann S, Golczyk H, et al. Horizontal genome transfer as an asexual path to the formation of new species. Nature, 2014, 511: 232-235
[19]
Li B-Y (李保印), Liu Y-S (刘用生), Zhou X-M (周秀梅), et al. Study on distant grafting of Salix and Popu-lus. Bulletin of Biology (生物学通报), 2004, 39(10): 19-20 (in Chinese)
[20]
Zhang S, Zhou R, Zhao HX, et al. iTRAQ-based quantitative proteomic analysis gives insight into sexually different metabolic processes of poplars under nitrogen and phosphorus deficiencies. Proteomics, 2016, 16: 614-628
[21]
Yemm EW, Willis AJ. The estimation of carbohydrates in plant extracts by anthrone. Biochemical Journal, 1954, 57: 508-514
[22]
Murata T, Akazawa T, Fukuchi S. Enzymic mechanism of starch of starch breakdown in germinating rice seeds. I. An analytical study. Plant Physiology, 1968, 43: 1899-1905
[23]
Dubois M, Gilles KA, Hamilton JK, et al. Colorimetric method of determination of sugars and related substances. Analytical Chemistry, 1956, 28: 350-356
[24]
Liu Y-S (刘用生). The theoretical and practical significance of plant distant grafting in ancient and modern China. Studies in the History of Natural Sciences (自然科学史研究), 2001, 20(4): 352-361 (in Chinese)
[25]
Shao G-Y (邵果园), Lu F-F (陆方方). In vitro distant grafting with an ISSR analysis. Journal of Zhejiang Forestry College (浙江农林大学学报), 2010, 27(4): 630-634 (in Chinese)
[26]
Lu Y-T (卢吟涛), Shao G-Y (邵果园), Lu F-F (陆方方). Experiment on in-vitro distant grafting of seven plant species. Journal of Zhejiang Forestry Science and Technology (浙江林业科技), 2013, 33(6): 57-60 (in Chinese)
[27]
Mudge K, Janick J, Scofield S, et al. A history of graf-ting. Horticultural Reviews, 2009, 35: 437-493
[28]
Zhao Y (赵 燕), Dong W-Y (董雯怡), Zhang Z-Y (张志毅), et al. Effects of fertilization on seedling growth and photosynthesis of hybrid clone seedlings of Populus tomentosa. Scientia Silvae Sinicae (林业科学), 2010, 46(4): 70-77 (in Chinese)
[29]
McDowell N, Pockman WT, Allen CD, et al. Mechanisms of plant survival and mortality during drought: Why do some plants survive while others succumb to drought? New Phytologist, 2008, 178: 719-739
[30]
Temperini O, Calabrese N, Temperini A, et al. Grafting artichoke onto cardoon rootstocks: Graft compatibility, yield and Verticillium wilt incidence. Scientia Horticulturae, 2013, 149: 22-27
[31]
Dong TF, Duan BL, Zhang S, et al. Growth, biomass allocation and photosynthetic responses are related to intensity of root severance and soil moisture conditions in the plantation tree Cunninghamia lanceolata. Tree Physio-logy, 2016, 36: 807-817
[32]
Kano M, Inukai Y, Kitano H, et al. Root plasticity as the key root trait for adaptation to various intensities of drought stress in rice. Plant and Soil, 2011, 342: 117-128
[33]
Lu G-C (卢广超), Xu J-X (许建新), Xue L (薛 立), et al. Comprehensive evaluation on photosynthetic and fluorescence characteristics in seedlings of 4 drought resistance species. Acta Ecologica Sinica (生态学报), 2013, 33(24): 7872-7881 (in Chinese)
[34]
Way DA, Seegobin SD, Sage RF. The effect of carbon and nutrient loading during nursery culture on the growth of black spruce seedlings: A six-year field study. New Forests, 2007, 34: 307-312
[35]
Adams HD, Germino MJ, Breshears DD, et al. Nonstructural leaf carbohydrate dynamics of Pinus edulis during drought-induced tree mortality reveal role for carbon metabolism in mortality mechanism. New Phytologist, 2013, 197: 1142-1151
[36]
Guo Q, Li J, Zhang YB, et al. Species-specific competition and N fertilization regulate non-structural carbohydrate contents in two Larix species. Forest Ecology and Management, 2016, 364: 60-69
[37]
Muller B, Pantin F, Génard M, et al. Water deficits uncouple growth from photosynthesis, increase C content, and modify the relationships between C and growth in sink organs. Journal of Experimental Botany, 2011, 62: 1715-1729
[38]
Blum A. Osmotic adjustment is a prime drought stress adaptive engine in support of plant production. Plant, Cell & Environment, 2017, 40: 4-10
[39]
Myers JA, Kitajima K. Carbohydrate storage enhances seedling shade and stress tolerance in a neotropical forest. Journal of Ecology, 2007, 95: 383-395
[40]
Wiley E, Huepenbecker S, Casper BB, et al. The effects of defoliation on carbon allocation: Can carbon limitation reduce growth in favour of storage? Tree Physio-logy, 2013, 33: 1216-1228
[41]
O’Brien MJ, Leuzinger S, Philipson CD, et al. Drought survival of tropical tree seedlings enhanced by non-structural carbohydrate levels. Nature Climate Change, 2014, 4: 710-714
[42]
Pan Q-M (潘庆民), Han X-G (韩兴国), Bai Y-F (白永飞), et al. Advances in physiology and ecology studies on stored non-structure carbohydrates in plants. Chinese Bulletin of Botany (植物学通报), 2002, 19(1): 30-38 (in Chinese)
[43]
Li N-N (李娜妮), He N-P (何念鹏), Yu G-R (于贵瑞). Evaluation of leaf non-structural carbohydrate contents in typical forest ecosystems in northeast China. Acta Ecologica Sinica (生态学报), 2016, 36(2): 430-438 (in Chinese)
[44]
Aronsson P, Perttu K. Willow vegetation filters for wastewater treatment and soil remediation combined with biomass production. The Forestry Chronicle, 2001, 77: 293-299
[45]
Kuzovkina YA, Knee M, Quigley MF. Cadmium and copper uptake and translocation in five willow (Salix L.) species. International Journal of Phytoremediation, 2004, 6: 269-287