Abstract
Root branching order supports a powerful approach to understanding complex root systems; however, how the pattern of root morphological characteristics, tissue carbon (C) and nitrogen (N) concentrations, and root lifespan are related to anatomical features of variable root orders for mature shrubs (∼19 years old) in sandy habitats is still unclear. In this study, these relationships were investigated for three typical shrubs in Horqin Sand Land, Northeast China. Root diameter, individual root length, tissue carbon concentration, C:N ratio, root lifespan, root cross-sectional area (CSA), stele CSA, proportion of stele in root CSA, mean xylem vessel CSA and the number of xylem vessels all increased with root order for the three shrubs, while specific root length and nitrogen concentration decreased with root order. The combined root biomass of the first two orders accounted for more than 63% of the first–fourth order root biomass for all the three shrubs. Proportion of stele to root CSA and number of xylem vessels of third-order root segments were significantly higher than that of the first two orders, and third-order roots showed secondary development with a continuous cork layer. All first-order and most second-order roots exhibited primary development, had an intact cortex, a lower proportion of stele to root CSA, and a smaller number of vessels. Our research suggests that the first two order roots of shrubs in sandy habitats are responsible mainly for absorption, and that they play a major role in root turnover and C and N flux in the soil organic matter pool due to their high proportion of biomass and N concentration, as well as their short lifespan.
Similar content being viewed by others
References
Andersson PI, Majdi H (2005) Estimating root longevity at sites with long periods of low root mortality. Plant Soil 276:9–14
Brundrett MC (2002) Coevolution of roots and mycorrhizas of land plants. New Phytol 154:275–304
Comas LH, Eissenstat DM (2009) Patterns in root trait variation among 25 co-existing North American forest species. New Phytol 182:919–928
Comas LH, Bouma TJ, Eissenstat DM (2002) Linking root traits to potential growth rate in six temperate tree species. Ecophysiology 132:34–43
de Neergaard E, Lyshede OB, Gahoonia TS, Care D, Hooker JE (2000) Anatomy and histology of roots and root-soil boundary. In: Smit AL, Bengough AG, Engels C, Noordwijk M, Pellerin S, Geijn SC (eds) Root methods: a handbook. Springer, Berlin, pp 33–74
Eissenstat DM (1992) Costs and benefits of constructing roots of small diameter. J Plant Nutr 15:763–782
Eissenstat DM, Achor DS (1999) Anatomical characteristics of roots of citrus rootstocks that vary in specific root length. New Phytol 141:309–321
Eissenstat DM, Wells CE, Yanai RD, Whitbeck JL (2000) Building fine roots in a changing environment: implications for root longevity. New Phytol 147:33–42
Fahey TJ, Hughes JW (1994) Fine root dynamics in a northern hardwood forest ecosystem, Hubbard Brook experimental forest. J Ecol 82:533–548
Fitter AH (1982) Morphometric analysis of root systems: application of the technique and influence of soil fertility on root system development in two herbaceous species. Plant Cell Environ 5:313–322
Gill RA, Jackson RB (2000) Global patterns of root turnover for terrestrial ecosystems. New Phytol 147:13–31
Gill RA, Burke IC, Lauenroth WK, Milchunas DG (2002) Longevity and turnover of roots in the shortgrass steppe: influence of diameter and depth. Plant Ecol 159:241–251
Gower ST, Vogt KA, Grier CC (1992) Carbon dynamics of Rocky Mountain Douglas-fir: influence of water and nutrient availability. Ecol Monogr 62:43–65
Guo DL, Mitchell RJ, Hendricks JJ (2004) Fine root branch orders respond differentially to carbon source-sink manipulations in a longleaf pine forest. Oecologia 140:450–457
Guo DL, Li H, Mitchell RJ, Han W, Hendricks JJ, Fahey TJ, Hendrick RL (2008a) Fine root heterogeneity by branch order: exploring the discrepancy in root turnover estimates between minirhizotron and carbon isotopic methods. New Phytol 177:443–456
Guo DL, Mitchell RJ, Withington JM, Fan PP, Hendricks JJ (2008b) Endogenous and exogenous controls of root life span, mortality and nitrogen flux in a longleaf pine forest: root branch order predominates. J Ecol 96:737–745
Guo DL, Xia M, Wei X, Chang W, Liu Y, Wang Z (2008c) Anatomical traits associated with absorption and mycorrhizal colonization are linked to root branch order in twenty-three chinese temperate tree species. New Phytol 180:673–683
He JS, Wang ZQ, Fang JY (2004) Underground ecology with global changes: problems and prospects (in Chinese). Chin Sci Bull 49:1226–1233
Hendrick RL, Pregitzer KS (1993) The dynamics of fine root, length, biomass, and nitrogen content in two northern hardwood ecosystems. Can J For Res 23:2507–2520
Hishi T, Takeda H (2005) Dynamics of heterorhizic root systems: protoxylem groups within the fine-root system of Chamaecyparis obtuse. New Phytol 167:509–521
Iversen CM, Ledford J, Norby RJ (2008) CO2 enrichment increases carbon and nitrogen input from fine roots in a deciduous forest. New Phytol 179:837–847
Kenrich P (2002) The origin of roots. In: Waisel Y, Eshel E, Kafkafi U (eds) Plant root: the hidden half. Dekker, New York, pp 1–15
Knute JN, James WR (1992) Fine root production estimates and below-ground carbon allocation in forest ecosystems. Ecology 73:1139–1147
Lux A, Luxova M, Abe J, Morita S (2004) Root cortex: structural and functional variability and responses to environmental stress (in Japanese). Root Res 13:117–131
McCrady RL, Comerford NB (1998) Morphological and anatomical relationships of Loblolly pine fine roots. Trees 12:431–437
Nelson DW, Sommers LE (1982) Total carbon, organic carbon and organic matter. In: Page AL, Miller RH, Keeney DR (eds) Methods of soil analysis. ASA, Madison, pp 539–577
Pregitzer KS, Kubiske ME, Yu CK, Hendrick RL (1997) Relationships among root branch order, carbon, and nitrogen in four temperate species. Oecologia 111:302–308
Pregitzer KS, DeForest JL, Burton AJ, Allen MF, Ruess RW, Hendrick RL (2002) Fine root architecture of nine North American trees. Ecol Monogr 72:293–309
Reich PB, Walters MB, Ellsworth DS (1992) Leaf life-span in relation to leaf, plant, and stand characteristics among diverse ecosystems. Ecolo Monogr 62:365–392
Schoettle AW, Fahey TJ, Shoettle AW (1994) Foliage and fine root longevity in pines. Ecol Bull 43:136–153
Shi W, Wang ZQ, Liu JL, Gu JC, Guo DL (2008) Fine root morphology of twenty hardwood species in Mao-er Shan natural secondary forest in northeastern China (in Chinese). J Plant Ecol 32:1217–1226
Soukup A, Malá J, Hrubcová M, Kálal J, Votrubová O, Cvikrová M (2004) Differences in anatomical structure and lignin content of roots of pedunculate oak and wild cherry-tree plantlets during acclimation. Biol Planta 48:481–489
Taylor JH, Peterson CA (2000) Morphometric analysis of Pinus banksiana Lamb. root anatomy during a 3-month field study. Trees 14:239–247
Tierney GL, Fahey TJ (2001) Evaluating minirhizotron estimates of fine root longevity and production in the forest floor. Plant Soil 229:167–176
Trumbore SE, Gaudinski JB (2003) The secret lives of roots. Science 302:1344–1345
Valenzuela-Estrada LR, Vera-Caraballo V, Ruth LE, Eissenstat DM (2008) Root anatomy, morphology, and longevity among root orders in Vaccinium corymbosum (Ericaceae). Am J Bot 95:1506–1514
Vogt KA, Grier CC, Sprugel DG, Vogt DJ (1986) Overestimation of net root production: a real or imaginary problem? Ecology 67:577–579
Wang ZQ, Guo DL, Wang XR, Gu JC, Mei L (2006) Fine root architecture, morphology, and biomass of different branch orders of two Chinese temperate tree species. Plant Soil 288:155–171
Watson CA, Ross JM, Bagnaresi U, Minotta GF, Roffi F, Atkinson D, Black KE, Hooker JE (2000) Environment-induced modifications to root longevity in Lolium perenne and Trifolium repens. Ann Bot 85:397–401
Wells CE, Eissenstat DM (2003) Beyond the roots of young seedlings: the influence of age and order on fine root physiology. J Plant Growth Regul 21:324–334
Wells CE, Glenn DM, Eissenstat DM (2002) Changes in the risk of fine-root mortality with age: a case study in peach, Prunus persica (Rosaceae). Am J Bot 89:79–87
West JB, Espeleta JF, Donovan LA (2003) Root longevity and phenology differences between two co-occurring savanna bunchgrasses with different leaf habits. Funct Ecol 17:20–28
Withington JM, Reich PB, Oleksyn J, Eissenstat DM (2006) Comparisons of structure and life span in roots and leaves among temperate trees. Ecol Monogr 76:381–398
Yanai RD, Fahey TJ, Miller SL (1995) Efficiency of nutrient acquisition by fine roots and mycorrhizae. In: Smith WK, Hinkley TM (eds) Resource physiology of conifers: acquisition, allocation, and utilization. Academic, New York, pp 75–103
Zhao AF (1994) Morphology, distribution and dynamics of root systems of Artemisia halodendron and Caragana microphylla (in Chinese). Grassland of China 3:15–19
Zhao HL, Zhou RL, Su YZ, Zhang H, Zhao LY, Drake S (2007) Shrub facilitation of desert land restoration in the Horqin Sand Land of Inner Mongolia. Ecol Eng 31:1–8
Acknowledgments
We are grateful to two anonymous reviewers for valuable comments on our manuscript. We also appreciate our colleagues and several other research workers at the NMDS for constructive criticism and help. This study was supported financially by the Chinese National Natural Science Foundation (2009CB421303-4, 40871004 and 30972422), and we also appreciate this financial support.
Author information
Authors and Affiliations
Corresponding author
Additional information
Responsible Editor: Tibor Kalapos.
Rights and permissions
About this article
Cite this article
Huang, G., Zhao, Xy., Zhao, Hl. et al. Linking root morphology, longevity and function to root branch order: a case study in three shrubs. Plant Soil 336, 197–208 (2010). https://doi.org/10.1007/s11104-010-0466-3
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s11104-010-0466-3