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Biogeochemistry

, Volume 4, Issue 3, pp 265–276 | Cite as

Nutrient reabsorption efficiency and the response to phosphorus fertilization in the desert shrubLarrea tridentata (DC.) Cov.

  • Kate Lajtha
Article

Abstract

A field fertilization experiment demonstrated that growth ofLarrea tridentata was not limited by phosphorus, even though soils contained high levels of pedogenic carbonates that can potentially fix high amounts of phosphorus. Nutrient reabsorption efficiencies in unfertilized shrubs ranged from 72–86% for P, making nutrient reabsorption a very effective nutrient conservation mechanism. Absolute amounts of N and P reabsorption increased with N and P concentrations in leaves, with reabsorption being greater during drought stress than during rapid leaf growth. However, only N reabsorption efficiency increased with increasing plant N status. A model was developed to explain patterns of nutrient reabsorption efficiencies over large gradients in nutrient availability.

Key words

nutrient reabsorption efficiency Larrea tridentata nutrient use phosphorus cycling desert ecosystems soil carbonates 

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References

  1. Attiwill, P.M., H.B. Guthrie & R. Leuning (1978) Nutrient cycling in a Eucalyptus obliqua (L'Herit.) forest. I. Litter production and nutrient return. Australian Journal of Botany 26: 79–91Google Scholar
  2. Avnimelech, Y. (1983) Phosphorus and calcium carbonate solubilities in Lake Kenneret. Limnology and Oceanography 28: 640–645Google Scholar
  3. Bamberg, S.A., A.T. Vollmer, G.E. Kleinkopf & T.L. Ackerman (1976) A comparison of seasonal primary production of Mojave desert shrubs during wet and dry years. American Midland Naturalist 95: 398–405Google Scholar
  4. Birk, E.M. & P.M. Vitousek (1986) Nitrogen availability and nitrogen use efficiency in loblolly pine stands. Ecology 67: 69–79Google Scholar
  5. Burk, J.H. & W.A. Dick-Peddie (1973) Comparative production ofLarrea divaricata Cav. on three geomorphic surfaces in southern New Mexico. Ecology 54: 1094–1102Google Scholar
  6. Chang, C.W. (1953) Chemical properties of alkali soils in Mesilla Valley, New Mexico. Soil Science 75: 233–242Google Scholar
  7. Chapin, F.S. III (1983) Nitrogen and phosphorus nutrition and nutrient cycling by evergreen and deciduous understory shrubs in an Alaskan black spruce forest. Canadian Journal of Forest Research 13: 773–781Google Scholar
  8. Chapin, F.S. III & R.A. Kedrowski (1983) Seasonal changes in nitrogen and phosphorus fractions and autumn retranslocation in evergreen and deciduous taiga trees. Ecology 64: 376–391Google Scholar
  9. Chew, R.M. & A.E. Chew (1965) The primary productivity of a desert-shrub (Larrea tridentata) community. Ecological Monographs 35: 355–375Google Scholar
  10. Cole, C.V. & S.R. Olsen (1959) Phosphorous solubility in calcareous soils 1. Dicalcium phosphate activities in equilibrium solutions. Soil Science Society of America Proceedings 23: 116–118Google Scholar
  11. Comstock, J. & J. Ehleringer (1986) Canopy dynamics and carbon gain in response to soil water availability inEncelia frutescens Gray, a drought-deciduous shrub. Oecologia 68: 271–278Google Scholar
  12. Crawford, C.SD. & J.R. Gosz (1982) Desert ecosystems: their resources in space and time. Environmental Conservation 9: 181–195Google Scholar
  13. Dregne, H.E. (1976) Soils of arid regions. Elsevier, AmsterdamGoogle Scholar
  14. El-Ghonemy, A.A., A. Wallace & E.M. Romney (1978) Nutrient concentrations in the natural vegetation of the Mojave Desert. Soil Science 126: 219–229Google Scholar
  15. Ettershank, G., J.A. Ettershank, M. Bryant & W.G. Whitford (1978) Effects of nitrogen fertilization on primary productivity in a Chihuahuan Desert ecosystem. Journal of Arid Environments 1: 135–139Google Scholar
  16. Fife, D.N. & E.K.S. Nambiar (1984) Movement of nutrients in Radiata Pine needles in relation to the growth of shoots. Annals of Botany 54: 303–314Google Scholar
  17. Fisher, F.M., G.L. Cunningham & W.G. Whitford (in prep.) Effects of water and nitrogen amendments on creosotebush above ground production and reproductive allocationGoogle Scholar
  18. Gile, L.H., J.W. Hawley & R.B. Grossman (1981) Soils and geomorphology in the Basin and Range area of southern New Mexico—Guidebook to the Desert Project. Memoir 39, New Mexico Bureau of Mines and Mineral Resources, Socorro, New MexicoGoogle Scholar
  19. Hocking, P.J. (1982) Effect of water stress on redistribution of nutrients from leaflets of narrowleaved lupin (Lupinus angustifolius L.). Annals of Botany 49: 541–543Google Scholar
  20. Hurlbert, S.H. (1984) Pseudoreplication and the design of ecological field experiments. Ecological Monographs 54: 187–211Google Scholar
  21. Jonasson, S. & F.S. Chapin III (1985) Significance of sequential leaf development for nutrient balance of the cotton sedge,Eriophorum vaginatum L. Oecologia 67: 511–518Google Scholar
  22. Lajtha, K. (1986) The biogeochemistry of phosphorus cycling and phosphorus availability in a desert ecosystem. Dissertation. Duke University, Durham, North Carolina, USAGoogle Scholar
  23. Lennon, J.M., J.D. Aber & J.M. Melillo (1985) Primary production and nitrogen allocation of field grown sugar maples in relation to nitrogen availability. Biogeochemistry 1: 135–154Google Scholar
  24. Lowther, J.R. (1980) Use of a single sulfuric acid-hydrogen peroxide digest for the analysis ofPinus radiata needles. Communications in Soil Science and Plant Analysis 11: 175–188Google Scholar
  25. Ludwig, J.A. & W.G. Whitford (1981) Short-term water and energy flow in arid ecosystems. In: D.W. Goodall & R.A. Perry (Eds) Arid-Land Ecosystems: Structure, Functioning and Management. Volume 2 (pp. 271–299) Cambridge University Press, CambridgeGoogle Scholar
  26. Marion, G.M. & K.L. Babcock (1977) The solubilities of carbonates and phosphates in calcareous soil suspensions. Soil Science Society of America Journal 41: 724–728Google Scholar
  27. McCaslin, B.D. & R.J. Gledhill (1980) Alfalfa fertilization in New Mexico. Bulletin 675. Agricultural Experiment Station, Las Cruces, New MexicoGoogle Scholar
  28. Miller, H.G., J.M. Cooper & J.D. Miller (1976) Effect of nitrogen supply on nutrients in litterfall and crown leaching in a stand of Corsican pine. Journal of Applied Ecology 13: 233–248Google Scholar
  29. Ostman, N.L. & G.T. Weaver (1982) Autumnal nutrient transfers by retranslocation, leaching and litterfall in a chestnut-oak forest in southern Illinois. Canadian Journal of Forest Research 12: 40–51Google Scholar
  30. Ryan, D.F. & F.H. Bormann (1982) Nutrient resorption in northern hardwood forests. BioScience 32: 29–32Google Scholar
  31. SAS Institute Inc. (1982) SAS user's guide: statistics. SAS Institute Inc., Cary, North CarolinaGoogle Scholar
  32. Schlesinger, W.H. (1982) Carbon storage in the caliche of arid soils: a case study from Arizona. Soil Science 133: 247–255Google Scholar
  33. Shaver, G.R. (1983) Mineral nutrition and leaf longevity inLedum palustris: the role of individual nutrients and the timing of the leaf mortality. Oecologia 56: 160–165Google Scholar
  34. Shaver, G.R. & J.M. Melillo (1984) Nutrient budgets of marsh plants: efficiency concepts and relation to availability. Ecology 65: 1491–1510Google Scholar
  35. Shreve, F. (1942) The desert vegetation of North America. Botanical Review 8: 195–246Google Scholar
  36. Simms, E.L. & D.S. Burdick (in press) Profile analysis of variance as a tool for analyzing correlated responses in experimental ecology. Biometrical JournalGoogle Scholar
  37. Staaf, H. (1982) Plant nutrient changes in beech leaves during senescence as influenced by site characters. Oceologia Plantarum 3: 161–170Google Scholar
  38. Stachurski, A. & J.R. Zimka (1975) Methods of studying forest ecosystems: leaf area, leaf production and withdrawal of nutrients from leaves of trees. Ekologia Polska 23: 637–648Google Scholar
  39. Technicon (1977) Individual/simultaneous determination of nitrogen and/or phosphorus in BD acid digests. Industrial Method 329-74W/B. Technicon Industrial Systems, Tarrytown, New YorkGoogle Scholar
  40. Turner, J. (1977) Effects of nitrogen availability on nitrogen cycling in a Douglas-fir stand. Forest Science 23: 307–316Google Scholar
  41. Vitousek, P. (1982) Nutrient cycling and nutrient use efficiency. The American Naturalist 119: 553–572Google Scholar
  42. Walbridge, M.R. (1986) Phosphorus availability in acid organic coastal plan soils. Dissertation. University of North Carolina, Chapel Hill, North Carolina, USAGoogle Scholar
  43. Wallace, A. & E.M. Romney (1972) Radioecology and ecophysiology of desert plants at the Nevada Test Site. US Atomic Energy Commission TID-26954, Office of Information Services, Springfield, VirginiaGoogle Scholar
  44. Williams, R.B. & K.L. Bell (1981) Nitrogen allocation in Mojave Desert winter annuals. Oecologia 48: 145–150Google Scholar

Copyright information

© Martinus Nijhoff/Dr W. Junk Publishers 1987

Authors and Affiliations

  • Kate Lajtha
    • 1
  1. 1.Department of BotanyDuke UniversityDurhamUSA

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