Skip to main content
Log in

Plant N capture from pulses: effects of pulse size, growth rate, and other soil resources

  • Community ecology
  • Published:
Oecologia Aims and scope Submit manuscript

Abstract

In arid ecosystems, the ability to rapidly capture nitrogen (N) from brief pulses is expected to influence plant growth, survival, and competitive ability. Theory and data suggest that N capture from pulses should depend on plant growth rate and availability of other limiting resources. Theory also predicts trade-offs in plant stress tolerance and ability to capture N from different size pulses. We injected K15NO3, to simulate small and large N pulses at three different times during the growing season into soil around the co-dominant Great Basin species Sarcobatus vermiculatus, Chrysothamnus nauseosus ssp. consimilis, and Distichlis spicata. Soils were amended with water and P in a partial factorial design. As predicted, all study species showed a comparable decline in N capture from large pulses through the season as growth rates slowed. Surprisingly, however, water and P availability differentially influenced the ability of these species to capture N from pulses. Distichlis N capture increased up to tenfold with water addition while Chrysothamnus N capture increased up to threefold with P addition. Sarcobatus N capture was not affected by water or P availability. Opposite to our prediction, Sarcobatus, the most stress tolerant species, captured less N from small pulses but more N from large pulses relative to the other species. These observations suggest that variation in N pulse timing and size can interact with variable soil water and P supply to determine how N is partitioned among co-existing Great Basin species.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3

Similar content being viewed by others

References

  • Aerts R, Chapin FS (2000) The mineral nutrition of wild plants revisited: a re-evaluation of processes and patterns. Adv Ecologic Res 30:1–67

    Article  CAS  Google Scholar 

  • Austin AT, Yahdjian L, Stark JM, Belnap J, Porporato A, Norton U, Ravetta D, Schaeffer SM (2004) Water pulses and biogeochemical cycles in arid and semiarid ecosystems. Oecologia 141:221–235

    Article  PubMed  Google Scholar 

  • BassiriRad H, Caldwell MM (1992) Temporal changes in root growth and 15N uptake and water relations of two tussock grass species recovering from water-stress. Physiol Plantarum 86:525–531

    Article  Google Scholar 

  • BassiriRad H, Tremmel DC, Virginia RA, Reynolds JF, de Soyza AG, Brunell MH (1999) Short-term patterns in water and nitrogen acquisition by two desert shrubs following a simulated summer rain. Plant Ecol 145:27–36

    Article  Google Scholar 

  • Bilbrough CJ, Caldwell MM (1997) Exploitation of springtime ephemeral N pulses by six Great Basin plant species. Ecology 78:231–243

    Google Scholar 

  • Bloom AJ, Chapin FS, Mooney HA (1985) Resource limitation in plants—an economic analogy. Ann Rev Ecol Syst 16:363–392

    Google Scholar 

  • Cabrera ML, Beare MH (1993) Alkaline persulfate oxidation for determining total nitrogen in microbial biomass extracts. Soil Sci Soc Am J 57:1007–1012

    Article  CAS  Google Scholar 

  • Chesson P, Pacala S, Neuhauser C (2001) Environmental niches and ecosystem functioning. In: Kingzig A, Pacala S, Tilman D (eds) The functional consequences of biodiversity. Princeton University Press, Princeton, New Jersey, pp 213–245

    Google Scholar 

  • Chesson P, Gebauer RLE, Schwinning S, Huntly N, Wiegand K, Ernest MSK, Sher A, Novoplansky A, Weltzin JF (2004) Resource pulses, species interactions, and diversity maintenance in arid and semi-arid environments. Oecologia 141:236–253

    Article  PubMed  Google Scholar 

  • Collier MD, Fotelli MN, Nahm M, Kopriva S, Rennenberg H, Hanke DE, Gessler A (2003) Regulation of nitrogen uptake by Fagus sylvatica on a whole plant level—interactions between cytokinins and soluble N compounds. Plant Cell Environ 26:1549–1560

    Article  CAS  Google Scholar 

  • Comstock JP, Ehleringer JR (1992) Plant adaptation in the Great-Basin and Colorado Plateau. Great Basin Nat 52:195–215

    Google Scholar 

  • Cui MY, Caldwell MM (1997a) A large ephemeral release of nitrogen upon wetting of dry soil and corresponding root responses in the field. Plant Soil 191:291–299

    Article  CAS  Google Scholar 

  • Cui M, Caldwell MM (1997b) Growth and nitrogen uptake by Agropyron desertorum and Pseudoroegneria spicata when exposed to nitrate pulses of different duration. Aust J Plant Physiol 24:637–642

    Article  Google Scholar 

  • Donovan LA, Richards JH (2000) Juvenile shrubs show differences in stress tolerance, but no competition or facilitation, along a stress gradient. J Ecol 88:1–16

    Article  Google Scholar 

  • Donovan LA, Richards JH, Muller MW (1996) Water relations and leaf chemistry of Chrysothamnus nauseosus ssp consimilis (Asteraceae) and Sarcobatus vermiculatus (Chenopodiaceae). Am J Bot 83:1637–1646

    Article  CAS  Google Scholar 

  • Donovan LA, Richards JH, Linton MJ (2003) Magnitude and mechanisms of disequilibrium between predawn plant and soil water potentials. Ecology 84:463–470

    Article  Google Scholar 

  • Drenovsky RE (2002) Effects of mineral nutrient deficiencies on plant performance in the desert shrubs Chrysothamnus nauseosus spp. consimilis and Sarcobatus vermiculatus. PhD Dissertation. University of California, Davis

  • Drenovsky RE, Richards JH (2004) Critical N:P values: predicting nutrient deficiencies in desert shrublands. Plant Soil 259:59–69

    Article  CAS  Google Scholar 

  • Drew MC, Saker LR (1975) Nutrient supply and the growth of seminal root systems in barely II localized compensatory increases in lateral root growth and rates of nitrate uptake when nitrate supply is restricted to only one part of the root system. J Exp Bot 26:79–90

    Article  CAS  Google Scholar 

  • Eissenstat DM, Caldwell MM (1988) Seasonal timing of root growth in favorable microsites. Ecology 69:870–873

    Article  Google Scholar 

  • Emery NC, Ewanchuk PJ, Bertness MD (2001) Competition and salt-marsh plant zonation: stress tolerators may be dominant competitors. Ecology 82:2471–2485

    Google Scholar 

  • Fisher FM, Parker LW, Anderson JP, Whitford WG (1987) Nitrogen mineralization in a desert soil - interacting effects of soil moisture and nitrogen fertilizer. Soil Sci Soc Am J 51:1033–1041

    Article  Google Scholar 

  • Fitter AH (1986) Spatial and temporal patterns of root activity in a species rich alluvial grassland. Oecologia 69:594–599

    Article  Google Scholar 

  • Forde BG (2002) Local and long-range signaling pathways regulating plant responses to nitrate. Ann Rev Plant Biol 53:203–224

    Article  CAS  Google Scholar 

  • Forster JC (1995) Soil nitrogen. In: Alef K, Nannipieri P (eds) Methods in applied soil microbiology and biochemistry. Academic, San Diego, pp 79–87

    Google Scholar 

  • Foyer CH, Valadier MH, Migge A, Becker TW (1998) Drought-induced effects on nitrate reductase activity and mRNA and on the coordination of nitrogen and carbon metabolism in maize leaves. Plant Physiol 117:283–292

    Article  PubMed  CAS  Google Scholar 

  • Gebauer RLE, Ehleringer JR (2000) Water and nitrogen uptake patterns following moisture pulses in a cold desert community. Ecology 81:1415–1424

    Google Scholar 

  • Gebauer RLE, Schwinning S, Ehleringer JR (2002) Interspecific competition and resource pulse utilization in a cold desert community. Ecology 83:2602–2616

    Google Scholar 

  • Gleeson SK, Good RE (2003) Root allocation and multiple nutrient limitation in the New Jersey Pinelands. Ecol Lett 6:220–227

    Article  Google Scholar 

  • Gleeson SK, Tilman D (1992) Plant allocation and the multiple limitation hypothesis. Am Nat 139:1322–1343

    Article  Google Scholar 

  • Goldberg D, Novoplansky A (1997) On the relative importance of competition in unproductive environments. J Ecol 85:409–418

    Article  Google Scholar 

  • Grime JP (1977) Evidence for existence of three primary strategies in plants and its relevance to ecological and evolutionary theory. Am Nat 111:1169–1194

    Article  Google Scholar 

  • Grime JP (1994) The role of plasticity in exploiting environmental heterogeneity. In: Caldwell MM, Pearcy RW (eds) Exploitation of environmental heterogeneity by plants. Academic, San Diego, pp 2–19

    Google Scholar 

  • Hodge A, Stewart J, Robinson D, Griffiths BS, Fitter AH (1999) Plant, soil fauna and microbial response to N-rich organic patches of contrasting temporal availability. Soil Biol Biochem 31:1517–1530

    Article  CAS  Google Scholar 

  • Hodge A, Robinson D, Fitter A (2000) Are microorganisms more effective than plants at competing for nitrogen? Trends Plant Sci 5:304–308

    Article  PubMed  CAS  Google Scholar 

  • Ivans CY, Leffler AJ, Spaulding U, Stark JM, Ryel RJ, Caldwell MM (2003) Root responses and nitrogen acquisition by Artemisia tridentata and Agropyron desertorum following small summer rainfall events. Oecologia 134:317–324

    PubMed  Google Scholar 

  • Jackson RB, Caldwell MM (1989) The timing and degree of root proliferation in fertile-soil microsites for three cold-desert perennials. Oecologia 81:149–153

    Google Scholar 

  • Jackson RB, Caldwell MM (1993) The scale of nutrient heterogeneity around individual plants and its quantification with geostatistics. Ecology 74:612–614

    Article  Google Scholar 

  • Jeuffroy MH, Ney B, Ourry A (2002) Integrated physiological and agronomic modeling of N capture and use within the plant. J Exp Bot 53:809–823

    Article  PubMed  CAS  Google Scholar 

  • Kaye JP, Hart SC (1997) Competition for nitrogen between plants and soil microorganisms. Trends Ecol Evol 12:139–143

    Article  Google Scholar 

  • Kim TH, Jung WJ, Lee BR, Yoneyama T, Kim HY, Kim KY (2003) P effects on N uptake and remobilization during regrowth of Italian ryegrass (Lolium multiflorum). Environ Exp Bot 50:233–242

    Article  CAS  Google Scholar 

  • Larigauderie A, Richards JH (1994) Root proliferation characteristics of seven perennial arid land grasses in nutrient-enriched microsites. Oecologia 99:102–111

    Article  Google Scholar 

  • Mamolos AP, Veresoglou DS (2000) Patterns of root activity and responses of species to nutrients in vegetation of fertile alluvial soil. Plant Ecol 148:245–253

    Article  Google Scholar 

  • Matzner SL, Richards JH (1996) Sagebrush (Artemisia tridentata Nutt) roots maintain nutrient uptake capacity under water stress. J Exp Bot 47:1045–1056

    Article  CAS  Google Scholar 

  • McKane RB, Grigal DF, Russelle MP (1990) Spatiotemporal differences in 15N uptake and the organization of an old-field plant community. Ecology 71:1126–1132

    Article  Google Scholar 

  • Miranda KM, Espey MG, Wink DA (2001) A rapid, simple spectrophotometric method for simultaneous determination of nitrate and nitrite. Nitric oxide. Biol Biochem 5:62–71

    CAS  Google Scholar 

  • Nadelhoffer KJ, Fry B (1994) Nitrogen isotope studies in forest ecosystems. In: Lajtha K, Michener R (eds) Stable isotopes in ecology. Blackwell, Oxford, pp 22–44

    Google Scholar 

  • Neff JC, Chapin FS, Vitousek PM (2003) Breaks in the cycle: dissolved organic nitrogen in terrestrial ecosystems. Front Ecol Environ 1:205–211

    Article  Google Scholar 

  • Neter J, Wasserman W, Kutner MH (1990) Applied linear statistical models: regression, analysis of variance, and experimental design. 3 edn. Irwin, Homewood

    Google Scholar 

  • Noy-Meir I (1973) Desert ecosystems: environments and producers. Ann Rev Ecol Syst 4:25–51

    Article  Google Scholar 

  • Nye P, Tinker P (1977) Solute movement in the soil-root system. University of California Press, Berkeley

    Google Scholar 

  • Peek MS, Forseth IN (2003) Microhabitat dependent responses to resource pulses in the aridland perennial, Cryptantha flava. J Ecol 91:457–466

    Article  Google Scholar 

  • Sah RN, Miller RO (1992) Spontaneous reaction for acid dissolution of biological tissues in closed vessels. Anal Chem 64:230–233

    Article  PubMed  CAS  Google Scholar 

  • SAS-Institute (2001) SAS/STAT user’s guide. Version 8. SAS Institute, Cary

  • Schjorring JK (1986) Nitrate and ammonium absorption by plants growing at a sufficient or insufficient level of phosphorus in nutrient solutions. Plant Soil 91:313–318

    Article  Google Scholar 

  • Seely B, Lajtha K (1997) Application of a 15N tracer to simulate and track the fate of atmospherically-deposited N of the costal forests of the Waquoit Bay Watershed, Cape Cod, MA. Oecologia 112:393–402

    Article  Google Scholar 

  • Smith SD, Monson RK, Anderson JE (1997) Physiological ecology of North American desert plants. Springer, Berlin, New York, Heidelberg

    Google Scholar 

  • Snyder KA, Donovan LA, James JJ, Tiller RL, Richards JH (2004) Extensive summer water pulses do not necessarily lead to canopy growth of Great Basin and northern Mojave Desert shrubs. Oecologia 141:325–334

    Article  PubMed  CAS  Google Scholar 

  • Stitt M (1999) Nitrate regulation of metabolism and growth. Curr Opin Plant Biol 2:178–186

    Article  PubMed  CAS  Google Scholar 

  • Tilman D (1988) Plant strategies and the dynamics and structure of plant communities. Princeton University Press, Princeton

    Google Scholar 

  • Vega-Jarquin C, Garcia-Mendoza M, Jablonowski N, Luna-Guido M, Dendooven L (2003) Rapid immobilization of applied nitrogen in saline-alkaline soils. Plant Soil 256:379–388

    Article  CAS  Google Scholar 

  • Yoder C, Caldwell M (2002) Effects of perennial neighbors and nitrogen pulses on growth and nitrogen uptake by Bromus tectorum. Plant Ecol 158:77–84

    Article  Google Scholar 

Download references

Acknowledgements

We thank S. Blazej, A. Breen, and R. O’Dell, for help with field and lab work, and R. Drenovsky, L. Jackson, and T. Young for manuscript review. This research was supported by the CA State Lands Commission (C99017), The Los Angeles Department of Water and Power, and NSF grants IBN-99-03004 and IBN-04-16581. Additional support was provided by the California Agricultural Experiment Station and a Jastro-Shields Research Fellowship. We are grateful to Alan Knapp and two anonymous reviewers for providing critical comments on an earlier version of the manuscript.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to J. J. James.

Additional information

Communicated by Alan Knapp

Rights and permissions

Reprints and permissions

About this article

Cite this article

James, J.J., Richards, J.H. Plant N capture from pulses: effects of pulse size, growth rate, and other soil resources. Oecologia 145, 113–122 (2005). https://doi.org/10.1007/s00442-005-0109-1

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00442-005-0109-1

Keywords

Navigation