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Rapid root elongation by phreatophyte seedlings does not imply tolerance of water table decline

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Despite high rates of root elongation during phreatophyte establishment, once connection to groundwater has occurred and leaf area develops, seedlings demonstrate limited capacity for root elongation in response to groundwater decline.

Abstract

In a water-limited environment, rapid root elongation immediately after germination can be critical for a plant to reach deeper water sources such as a water table to avoid water deficit stress. However, once plants have accessed a water table, their continued survival may depend on their ability to adapt their root distribution to changes in the depth to a water table. In glasshouse experiments using two Banksia species with contrasting water requirements, we investigated (1) the rate of root elongation by young seedlings in the presence of a shallow water table, and (2) whole plant response to rapid water table decline using older seedlings that had established root contact with a water table. The results of the first experiment agree with the hypothesis that the facultative phreatophyte, B. attenuata, has a faster rate of root elongation than the obligate phreatophyte, B. littoralis. These differences are likely related to the contrasting habitat preferences of the two species. Older seedlings in the second experiment demonstrated a water-saving response to a declining water table, rapidly closing stomata to limit water loss. Additionally, roots did not elongate to follow the water table and plants were quickly disconnected from the saturated zone. For the two phreatophytic Banksia species, the capacity for rapid root growth by young seedlings did not translate to an ability for established seedlings to adapt their root distribution to survive rapid water table decline.

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References

  • Arrowsmith N (1992) Gnangara Mound vegetation stress study—results of investigations. Water Authority of Western Australia, Perth

    Google Scholar 

  • Booth GD, Welch BL, Jacobson TLC (1990) Seedling growth rate of three subspecies of big sagebrush. J Range Manag 43:432–436

    Article  Google Scholar 

  • Canham, CA (2011) The response of Banksia roots to change in water table levels in a Mediterranean-type environment. PhD dissertation, School of Natural Sciences, Edith Cowan University, Perth

  • Canham CA, Froend RH, Stock WD (2009) Water stress vulnerability of four Banksia species in contrasting ecohydrological habitats on the Gnangara Mound, Western Australia. Plant Cell Environ 32:64–72

    Article  PubMed  Google Scholar 

  • Canham CA, Froend RH, Stock WD, Davies MD (2012) Dynamics of phreatophyte root growth relative to a seasonally fluctuating water table in a Mediterranean-type environment. Oecologia 170:909–916

    Article  PubMed  Google Scholar 

  • Cooper DJ, D’Amico DR, Scott ML (2003) Physiological and morphological response patterns of Populus deltoides to alluvial groundwater pumping. Environ Manag 31:215–226

    Article  Google Scholar 

  • Cowling RM, Lamont BB, Pierce SM (1987) Seed bank dynamics of four co-occurring Banksia species. J Ecol 75:289–302

    Article  Google Scholar 

  • Dalling JW, Hubbell SP (2002) Seed size, growth rate and gap microsite conditions as determinants of recruitment success for pioneer species. J Ecol 90:557–568

    Article  Google Scholar 

  • Eagleson PS (2002) Ecohydrology: Darwinian expression of vegetation form and function. Cambridge University Press, Cambridge

    Book  Google Scholar 

  • Evans CE, Etherington JR (1991) The effects of soil water potential on seedling growth of some British plants. New Phytol 118:571–579

    Article  Google Scholar 

  • Fenner M (1987) Seedlings. New Phytol 106:35–47

    Article  Google Scholar 

  • Frazer JM, Davis SD (1988) Differential survival of chaparral seedlings during the first summer drought after wildfire. Oecologia 76:215–221

    Article  Google Scholar 

  • Freeze RA, Cherry JA (1979) Groundwater. Prentice-Hall Inc., New Jersey

    Google Scholar 

  • Gonzalez E, Comin FA, Muller E (2010) Seed dispersal, germination and early seedling establishment of Populus alba L. under simulated water table declines in different substrates. Trees 24:151–163

    Article  Google Scholar 

  • Groom PK, Froend RH, Mattiske EM (2000) Impact of groundwater abstraction on a Banksia woodland, Swan Coastal Plain, Western Australia. Ecol Manag Restor 1:117–124

    Article  Google Scholar 

  • Groom PK, Lamont BB, Wright IW (2001) Lottery (stochastic) and non-lottery (biological) processes explain recruitment patterns among eight congeneric shrub species in southwestern Australia. J Mediterr Ecol 2:1–14

    Google Scholar 

  • Horton JL, Clark J (2001) Water table decline alters growth and survival of Salix gooddingii and Tamarix chinensis seedlings. For Ecol Manag 140:239–247

    Article  Google Scholar 

  • Imada S, Yamanaka N, Tamai S (2010) Fine-root growth, fine-root mortality, and leaf morphological change of Populus alba in response to fluctuating water tables. Trees 24:499–506

    Article  Google Scholar 

  • Jurado E, Westoby M (1992) Seedling growth in relation to seed size among species of arid Australia. J Ecol 80:407–416

    Article  Google Scholar 

  • Kranjcec J, Mahoney JM, Rood SB (1998) The responses of three riparian cottonwood species to water table decline. For Ecol Manag 110:77–87

    Article  Google Scholar 

  • Lamont BB, Groom PK (2013) Seeds as a source of carbon, nitrogen and phosphorus for seedling establishment in temperate regions: a synthesis. Am J Plant Sci 4:30–40

    Article  CAS  Google Scholar 

  • Leishman MR, Westoby M (1994) The role of seed size in seedling establishment in dry soil conditions—experimental evidence from semi-arid species. J Ecol 82:249–258

    Article  Google Scholar 

  • Leishman MR, Wright IJ, Moles AT, Westoby M (2000) The evolutionary ecology of seed size. In: Fenner M (ed) Seeds—the ecology of regeneration in plant communities. CAB International, Wallingford, pp 31–57

    Chapter  Google Scholar 

  • LeMaitre DC, Scott DF, Colvin C (1999) Review of information on interactions between vegetation and groundwater. Water SA 25:137–152

    Google Scholar 

  • Lewis J (2012) The application of ecohydrological groundwater indicators to hydrogeological conceptual models. Groundwater 50:679–689

    Article  CAS  Google Scholar 

  • Mahoney JM, Rood SB (1991) A device for studying the influence of declining water table on Poplar growth and survival. Tree Physiol 8:305–314

    Article  PubMed  Google Scholar 

  • Marshall DL (1986) Effect of seed size in seedling success in three species of Sesbania (Fabaceae). Am J Bot 73:457–464

    Article  Google Scholar 

  • McDowell N, Pockman WT, Allen CD, Breshears DD, Cobb N, Kolb T, Plaut J, Sperry J, West A, Williams DG, Yepez EA (2008) Mechanisms of plant survival and mortality during drought: why do some plants survive while others succumb to drought? New Phytol 178:719–739

    Article  PubMed  Google Scholar 

  • Meinzer OE (1923) Outline of groundwater hydrology with definitions. Water-supply paper 494. US Geological Survey

  • Naumburg E, Mata-Gonzalez R, Hunter R, McLendon T, Martin D (2005) Phreatophytic vegetation and groundwater fluctuations: a review of current research and application of ecosystem response modelling with an emphasis on Great Basin vegetation. Environ Manag 35:726–740

    Article  Google Scholar 

  • Nicotra AB, Babicka N, Westoby M (2002) Seedling root anatomy and morphology: an examination of ecological differentiation with rainfall using phylogenetically independent contrasts. Oecologia 130:136–145

    Article  Google Scholar 

  • Osunkoya OO, Ash JE, Graham AW, Hopkins MS (1993) Growth of tree seedlings in tropical rain forests of North Queensland. Aust J Trop Ecol 9:1–18

    Article  Google Scholar 

  • Padilla FM, Pugnaire FI (2007) Rooting depth and soil moisture control Mediterranean woody seedling survival during drought. Funct Ecol 21:489–495

    Article  Google Scholar 

  • Richards MB, Stock WD, Cowling RM (1995) Water relations of seedlings and adults of two fynbos Protea species in relation to their distribution patterns. Funct Ecol 9:575–583

    Article  Google Scholar 

  • Scott M, Shafroth P, Auble G (1999) Responses of riparian cottonwoods to alluvial water table declines. Environ Manag 23:347–358

    Article  Google Scholar 

  • Sommer B, Froend R (2011) Resilience of phreatophytic vegetation to groundwater drawdown: is recovery possible under a drying climate? Ecohydrology 4:67–82

    Article  Google Scholar 

  • Sparks JP, Black RA (1999) Regulation of water loss in populations of Populus trichocarpa: the role of stomatal control in the prevention of xylem cavitation. Tree Physiol 19:453–459

    Article  PubMed  Google Scholar 

  • Sperry JS, Hacke UG (2002) Desert shrub water relations with respect to soil characteristics and plant functional type. Funct Ecol 16:367–378

    Article  Google Scholar 

  • Stave J, Oba G, Eriksen AB, Nordal I, Stenseth BC (2005) Seedling growth of Acacia tortilis and Faidherbia albida in response to simulated groundwater tables. For Ecol Manag 212:367–375

    Article  Google Scholar 

  • Walters MB, Reich PB (2000) Seed size, nitrogen supply, and growth rate affect tree seedling survival in deep shade. Ecology 81:1887–1901

    Article  Google Scholar 

  • Zencich SJ, Froend RH, Turner JV, Gailitis V (2002) Influence of groundwater depth on the seasonal sources of water accessed by Banksia tree species on a shallow, sandy coastal aquifer. Oecologia 131:8–19

    Article  Google Scholar 

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Author contribution statement

W. Stock, R. Froend and C. Canham conceived and designed the experiments; C. Canham performed the experiments and analysed the data; C. Canham, R. Froend and W. Stock wrote the paper.

Acknowledgments

The authors wish to acknowledge the support of the Water Corporation of Western Australia and the Australian Research Council.

Conflict of interest

This research was financially supported by an Australian Postgraduate Award associated with Australian Research Council Linkage Project LP0669240, and the Water Corporation of Western Australia. The authors declare they have no further conflict of interest.

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Correspondence to Raymond H. Froend.

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Communicated by H. Rennenberg.

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Canham, C.A., Froend, R.H. & Stock, W.D. Rapid root elongation by phreatophyte seedlings does not imply tolerance of water table decline. Trees 29, 815–824 (2015). https://doi.org/10.1007/s00468-015-1161-z

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  • DOI: https://doi.org/10.1007/s00468-015-1161-z

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