Please wait a minute...
Journal of Arid Land  2015, Vol. 7 Issue (4): 462-474    DOI:
Research Articles     
Optimal root system strategies for desert phreatophytic seedlings in the search for groundwater
LI Changjun1,2,3,4,5, ZENG Fanjiang1,3,4*, ZHANG Bo1,3,4,5, LIU Bo1,3,4, GUO Zichun1,3,4,5, GAO Huanhuan1,3,4,5, TIYIP Tashpolat2
1 State Key Laboratory of Desert and Oasis Ecology, Xinjiang Institute of Ecology and Geography, Chinese Academy of Sciences, Urumqi 830011, China;
2 College of Resources and Environment Science, Xinjiang University, Urumqi 830046, China;
3 Cele National Station of Observation and Research for Desert Grassland Ecosystem, Xinjiang Institute of Ecology and Geography, Chinese Academy of Sciences, Urumqi 830011, China;
4 Key Laboratory of Biogeography and Bioresource in Arid Land, Xinjiang Institute of Ecology and Geography, Chinese Academy of Sciences, Urumqi 830011, China;
5 University of Chinese Academy of Sciences, Beijing 100049, China
Download:   PDF(457KB)
Export: BibTeX | EndNote (RIS)      

Abstract  Desert phreatophytes are greatly dependent on groundwater, but how their root systems adapt to different groundwater depths is poorly understood. In the present study, shoot and root growths of Alhagi sparsifolia Shap. seedlings were studied across a gradient of groundwater depths. Leaves, stems and roots of different orders were measured after 120 days of different groundwater treatments. Results indicated that the depth of soil wetting front and the vertical distribution of soil water contents were highly controlled by groundwater depths. The shoot growth and biomass of A. sparsifolia decreased, but the root growth and rooting depth increased under deeper groundwater conditions. The higher ratios of root biomass, root/shoot and root length/leaf area under deeper groundwater conditions implied that seedlings of A. sparsifolia economized carbon cost on their shoot growths. The roots of A. sparsifolia distributed evenly around the soil wetting fronts under deeper groundwater conditions. Root diameters and root lengths of all orders were correlated with soil water availabilities both within and among treatments. Seedlings of A. sparsifolia produced finer first- and second-order roots but larger third- and fourth-order roots in dry soils. The results demonstrated that the root systems of desert phreatophytes can be optimized to acquire groundwater resources and maximize seedling growth by balancing the costs of carbon gain.

Key wordsmega-dune      water cycle      observation      wet sand layer      Badain Jaran Desert     
Received: 17 September 2014      Published: 10 August 2015
Fund:  

This study is supported by the Joint Funds of National Natural Science Foundation of China (U1203201) and the National Natural Science Foundation of China (41371516, 31100144).

Corresponding Authors:
Cite this article:

LI Changjun, ZENG Fanjiang, ZHANG Bo, LIU Bo, GUO Zichun, GAO Huanhuan, TIYIP Ta. Optimal root system strategies for desert phreatophytic seedlings in the search for groundwater. Journal of Arid Land, 2015, 7(4): 462-474.

URL:

http://jal.xjegi.com/     OR     http://jal.xjegi.com/Y2015/V7/I4/462

Arndt S K, Kahmen A, Arampatsis C, et al. 2004. Nitrogen fixation and metabolism by groundwater-dependent perennial plants in a hyperarid desert. Oecologia, 141: 385–394.

Bartsch N. 1987. Responses of root systems of young Pinus sylvestris and Picea abies plants to water deficits and soil acidity. Canadian Journal of Forest Research, 17(8): 805–812.

Blum A. 2011. Plant Breeding for Water-Limited Environments. New York: Springer, 11–52.

Bruelheide H, Vonlanthen B, Jandt U, et al. 2010. Life on the edge–to which degree does phreatic water sustain vegetation in the periphery of the Taklamakan Desert?. Applied Vegetation Science, 13: 56–71.

Chaves M M. 1991. Effects of water deficits on carbon assimilation. Journal of Experimental Botany, 42: 1–16.

Chaves M M, Maroco J P, Pereira J S. 2003. Understanding plant responses to drought—from genes to the whole plant. Functional Plant Biology, 30: 239–264.

Comas L H, Eissenstat D M. 2004. Linking fine root traits to maximum potential growth rate among 11 mature temperate tree species. Functional Ecology, 18: 388–397.

Comas L H, Becker S R, Von Mark V C, et al. 2013. Root traits contributing to plant productivity under drought. Frontiers in Plant Science, 4: 442.

Cooper D J, Sanderson J S, Stannard D I, et al. 2006. Effects of long-term water table drawdown on evapotranspiration and vegetation in an arid region phreatophyte community. Journal of Hydrology, 325: 21–34.

Cui Y L, Shao J L. 2005. The role of ground water in arid/semiarid ecosystems, Northwest China. Groundwater, 43: 471–477.

Eissenstat D M. 1997. Trade-offs in root form and function. In: Jackson L E. Ecology in Agriculture. San Diego: Academic Press Inc., 173–199.

Eissenstat D M, Wells C E, Yanai R D, et al. 2000. Building roots in a changing environment: implications for root longevity. New Phytologist, 147: 33–42.

Elmore A J, Manning S J, Mustard J F, et al. 2006. Decline in alkali meadow vegetation cover in California: the effects of groundwater extraction and drought. Journal of Applied Ecology, 43: 770–779.

Gerla P J. 1992. The relationship of water-table changes to the capillary fringe, evapotranspiration, and precipitation in intermittent wetlands. Wetlands, 12: 91–98.

Gries D, Zeng F J, Foetzki A, et al. 2003. Growth and water relations of Tamarix ramosissima and Populus euphratica on Taklamakan Desert dunes in relation to depth to a permanent water table. Plant, Cell and Environment, 26: 725–736.

Gui D W, Zeng F J, Liu Z, et al. 2013. Root characteristics of Alhagi sparsifolia seedlings in response to water supplement in an arid region, northwestern China. Journal of Arid Land, 5: 542–551.

Hodge A. 2004. The plastic plant: root responses to heterogeneous supplies of nutrients. New Phytologist, 162: 9–24.

Horton J L, Clark J L. 2001. Water table decline alters growth and survival of Salix gooddingii and Tamarix chinensis seedlings. Forest Ecology and Management, 140: 239–247.

Horton J L, Kolb T E, Hart S C. 2001. Responses of riparian trees to interannual variation in ground water depth in a semi-arid river basin. Plant, Cell and Environment, 24: 293–304.

Imada S, Yamanaka N, Tamai S. 2008. Water table depth affects Populus alba fine root growth and whole plant biomass. Functional Ecology, 22: 1018–1026.

Kobe R K, Iyer M, Walters M B. 2010. Optimal partitioning theory revisited: nonstructural carbohydrates dominate root mass responses to nitrogen. Ecology, 91: 166–179.

Körner C, Renhardt U. 1987. Dry matter partitioning and root length/leaf area ratios in herbaceous perennial plants with diverse altitudinal distribution. Oecologia, 74: 411–418.

Li H F, Zeng F J, Gui D W, et al. 2013. Effects of cutting and burning on regeneration of Alhagi sparsifolia Shap. on the southern fringe of the Taklamakan Desert, North-west China. The Rangeland Journal, 34: 389–397.

Li X Y, Lin L S, Zhao Q, et al. 2010. Influence of groundwater depth on species composition and community structure in the transition zone of Cele oasis. Journal of Arid Land, 2: 235–242.

Luke McCormack M, Adams T S, Smithwick E A H, et al. 2012. Predicting fine root lifespan from plant functional traits in temperate trees. New Phytologist, 195: 823–831.

Manes F, Vitale M, Donato E, et al. 2006. Different ability of three Mediterranean oak species to tolerate progressive water stress. Photosynthetica, 44(3): 387–393.

Markesteijn L, Poorter L. 2009. Seedling root morphology and biomass allocation of 62 tropical tree species in relation to drought- and shade-tolerance. Journal of Ecology, 97: 311–325.

Maroco J P, Pereira J S, Manuela Chaves M. 2000. Growth, photosynthesis and water-use efficiency of two C4 Sahelian grasses subjected to water deficits. Journal of Arid Environments, 45: 119–137.

Naumburg E, Mata-Gonzalez R, Hunter R G, et al. 2005. Phreatophytic vegetation and groundwater fluctuations: a review of current research and application of ecosystem response modeling with an emphasis on Great Basin vegetation. Environmental Management, 35: 726–740.

Neumann R B, Cardon Z G. 2012. The magnitude of hydraulic redistribution by plant roots: a review and synthesis of empirical and modeling studies. New Phytologist, 194: 337–352.

Ostonen I, Püttsepp Ü, Biel C, et al. 2007. Specific root length as an indicator of environmental change. Plant Biosystems, 141(3): 426–442.

Padilla F M, Pugnaire F I. 2007. Rooting depth and soil moisture control Mediterranean woody seedling survival during drought. Functional Ecology, 21: 489–495.

Poorter H, Nagel O. 2000. The role of biomass allocation in the growth response of plants to different levels of light, CO2, nutrients and water: a quantitative review. Functional Plant Biology, 27: 595–607.

Pregitzer K S. 2002. Fine roots of trees–a new perspective. New Phytologist, 154: 267–270.

Pregitzer K S, DeForest J L, Burton A J, et al. 2002. Fine root architecture of nine North American trees. Ecological Monographs, 72: 293–309.

Rains M C, Mount J F, Larsen E W. 2004. Simulated changes in shallow groundwater and vegetation distributions under different reservoir operations scenarios. Ecological Applications, 14: 192–207.

Rundel P W, Nobel P S, Atkinson D. 1991. Structure and function in desert root systems. In: Atkinson D. Plant Root Growth: An Ecological Perspective. Oxford: Blackwell Scientific Publications, 349–378.

Ryser P, Eek L. 2000. Consequences of phenotypic plasticity vs. interspecific differences in leaf and root traits for acquisition of aboveground and belowground resources. American Journal of Botany, 873: 402–411.

Stromberg J C, Tiller R, Richter B. 1996. Effects of groundwater decline on riparian vegetation of semiarid regions: the San Pedro, Arizona. Ecological Applications, 6: 113–131.

Thomas F M, Foetzki A, Arndt S K, et al. 2006. Water use by perennial plants in the transition zone between river oasis and desert in NW China. Basic and Applied Ecology, 7: 253–267.

Thomas F M, Foetzki A, Gries D, et al. 2008. Regulation of the water status in three co-occurring phreatophytes at the southern fringe of the Taklamakan Desert. Journal of Plant Ecology, 1: 227–235.

Van Wijk M T, Bouten W. 2001. Towards understanding tree root profiles: simulating hydrologically optimal strategies for root distribution. Hydrology and Earth System Sciences, 5: 629–644.

Vonlanthen B, Zhang X M, Bruelheide H. 2010. On the run for water–root growth of two phreatophytes in the Taklamakan Desert. Journal of Arid Environments, 74: 1604–1615.

Vonlanthen B, Zhang X M, Bruelheide H. 2011. Establishment and early survival of five phreatophytes of the Taklamakan Desert. Flora-Morphology, Distribution, Functional Ecology of Plants, 206: 100–106.

Wang G L, Fahey T J, Xue S. 2013. Root morphology and architecture respond to N addition in Pinus tabuliformis, west China. Oecologia, 171: 583–590.

Xia M X, Guo D L, Pregitzer K S. 2010. Ephemeral root modules in Fraxinus mandshurica. New Phytologist, 188: 1065–1074.

Yanai R D, Fahey T J, Miller S L. 1995. Efficiency of nutrient acquisition by fine roots and mycorrhizae. In: Smith W K, Hinckley T M. Resource Physiology of Conifers. New York: Academic, 75–103.

Zeng F J, Zhang X M, Foetzki A, et al. 2002. Water relation characteristics of Alhagi sparsifolia and consequences for a sustainable management. Science in China Series D: Earth Sciences, 45: 125–131.

Zeng F J, Bleby T M, Landman P A, et al. 2006. Water and nutrient dynamics in surface roots and soils are not modified by short-term flooding of phreatophytic plants in a hyper arid desert. Plant and Soil, 279: 129–139.

Zeng F J, Lu Y, Guo H F, et al. 2012. Ecological characteristics of Alhagi sparsifolia Shap. seedling roots under different irrigation treatments. Russian Journal of Ecology, 43: 196–203.

 
[1] JIN Junfang, YIN Shuyan, YIN Hanmin. Impact of land use/land cover types on surface humidity in northern China in the early 21st century[J]. Journal of Arid Land, 2022, 14(7): 705-718.
[2] ZHANG Kai, TIAN Jianjin, QU Jianjun, ZHAO Liming, LI Sheng. Sheltering effect of punched steel plate sand fences for controlling blown sand hazards along the Golmud-Korla Railway: Field observation and numerical simulation studies[J]. Journal of Arid Land, 2022, 14(6): 604-619.
[3] MENG Nan, WANG Nai'ang, ZHAO Liqiang, NIU Zhenmin, SUN Jiaqi. Wind regimes and associated sand dune types in the hinterland of the Badain Jaran Desert, China[J]. Journal of Arid Land, 2022, 14(5): 473-489.
[4] YAN Min, ZUO Hejun, WANG Haibing, DONG Zhi, LI Gangtie. Snow resisting capacity of Caragana microphylla and Achnatherum splendens in a typical steppe region of Inner Mongolia, China[J]. Journal of Arid Land, 2020, 12(2): 294-302.
[5] Yupeng LI, Yaning CHEN, Zhi LI. Effects of land use and cover change on surface wind speed in China[J]. Journal of Arid Land, 2019, 11(3): 345-356.
[6] Jinhu ZHANG, Nai'ang WANG, Zhenmin NIU, Jie SUN, Chunyu DONG, LyuLyu ZHANG. Stable isotope analysis of water sources for Tamarix laxa in the mega-dunes of the Badain Jaran Desert, China[J]. Journal of Arid Land, 2018, 10(6): 821-832.
[7] Jie SUN, Wenfeng HU, Nai'ang WANG, Liqiang ZHAO, Ran AN, Kai NING, Xunhe ZHANG. Eddy covariance measurements of water vapor and energy flux over a lake in the Badain Jaran Desert, China[J]. Journal of Arid Land, 2018, 10(4): 517-533.
[8] WANG Minzhong, WEI Wenshou, HE Qing, YANG Yuhui, FAN Lei, ZHANG Jiantao. Summer atmospheric boundary layer structure in the hinterland of Taklimakan Desert, China[J]. Journal of Arid Land, 2016, 8(6): 846-860.
[9] Jun WEN, ZhongBo SU, TangTang ZHANG, Hui TIAN, YiJian ZENG, Rong LIU, Yue KANG, Rogier van der VELDE. New evidence for the links between the local water cycle and the underground wet sand layer of a mega-dune in the Badain Jaran Desert, China[J]. Journal of Arid Land, 2014, 6(4): 371-377.