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RESEARCH ARTICLE

A quantitative top-down view of interactions between stresses: theory and analysis of nitrogen–water co-limitation in Mediterranean agro-ecosystems

Victor O. Sadras
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CSIRO – APSRU, Waite Campus; Present address: South Australian Research & Development Institute, Waite Research Precinct, Urrbrae, SA 5064, Australia. Email: sadras.victor@saugov.sa.gov.au

Australian Journal of Agricultural Research 56(11) 1151-1157 https://doi.org/10.1071/AR05073
Submitted: 7 March 2005  Accepted: 13 July 2005   Published: 29 November 2005

Abstract

The multiple factors constraining the growth, reproduction, and survival of diverse organisms are often non-additive. Research of interacting factors generally involves conceptual models that are specific for target organism, type of stress, and process. As a complement to this reductionist, bottom-up view, in this review I discuss a quantitative top-down approach to interacting stresses based on co-limitation theory.

Firstly, co-limitation theory is revised. Co-limitation is operationally identified when the output response of a biological system (e.g. plant or population growth) to two or more inputs is greater than its response to each factor in isolation. The hypothesis of Bloom, Chapin, and Mooney, that plant growth is maximised when it is equally limited by all resources, is reworded in terms of co-limitation and formulated in quantitative terms, i.e. for a given intensity of aggregate stress, plant growth is proportional to degree of resource co-limitation. Emphasis is placed on the problems associated with the quantification of co-limitation. It is proposed that seasonal indices of nitrogen and water stress calculated with crop simulation models can be integrated in indices accounting for the aggregated intensity of water and nitrogen stress (SWN), the degree of water and nitrogen co-limitation (CWN), and the integrated effect of stress and co-limitation (SCWN = CWN/SWN). The expectation is that plant growth and yield should be an inverse function of stress intensity and a direct function of co-limitation, thus proportional to SCWN.

Secondly, the constraints imposed by water and nitrogen availability on yield and water use efficiency of wheat crops are highlighted in case studies of low-input farming systems of south-eastern Australia.

Thirdly, the concept of co-limitation is applied to the analysis of (i) grain yield responses to water–nitrogen interactions, and (ii) trade-offs between nitrogen- and water-use efficiency. In agreement with theoretical expectations, measured grain yield is found to be proportional to modelled SCWN. Productivity gains associated with intensification of cropping practices are interpreted in terms of a trade-off, whereby water-use efficiency is improved at the expense of nitrogen-use efficiency, thus leading to a higher degree of resource co-limitation.

Additional keywords: complexity, resources, water-use efficiency, yield, marginal product, modelling, nitrogen, wheat, trade-off.


Acknowledgments

I thank Gabriela Borgognone, Pablo Calviño, Terry Chapin, David Connor, Laura Echarte, José Facelli, Claudio Ghersa, and Garry O’Leary for valuable discussions, and the GRDC of Australia for financial support (Project CSO212).


References


Angus JF, Bowden JW, Keating BA (1993) Modelling nutrient responses in the field. Plant and Soil 155–156, 57–66.
Crossref | GoogleScholarGoogle Scholar | accessed 3 April 2003.

Sih A, Goran E, Wooster D (1998) Emergent impacts of multiple predators on prey. Trends in Ecology and Evolution 13, 350–355.
Crossref | GoogleScholarGoogle Scholar | open url image1

Sinclair TR, Park WI (1993) Inadequacy of the Liebig limiting-factor paradigm for explaining varying crop yields. Agronomy Journal 85, 742–746. open url image1

de Varennes A, Melo-Abreu JP, Ferreira ME (2002) Predicting the concentration and uptake of nitrogen, phosphorus and potasium by field-grown green beans under non-limiting conditions. European Journal of Agronomy 17, 63–72.
Crossref | GoogleScholarGoogle Scholar | open url image1

Olde Venterink H, van der Vliet RE, Wassen MJ (2001) Nutrient limitation along a productive gradient in wet meadows. Plant and Soil 234, 171–179.
Crossref | GoogleScholarGoogle Scholar | open url image1

Verhoeven JTA, Koerselman W, Meuleman AFM (1996) Nitrogen- or phosphorus-limited growth in herbaceous, wet vegetation: relations with atmospheric inputs and management regimes. Trends in Ecology and Evolution 11, 494–497.
Crossref | GoogleScholarGoogle Scholar | open url image1

Waring GL, Cobb NS (1992) The impact of plant stress on herbivore population dynamics. ‘Insect–plant interactions’. (Ed. EA Bernays) pp. 167–226. (CRC Press: Boca Raton, FL)

Witt C, Dobermann A, Abdulrachman S, Gines HC, Guanghuo W , et al. (1999) Internal nutrient efficiencies of irrigated lowland rice in tropical and subtropical Asia. Field Crops Research 63, 113–138.
Crossref | GoogleScholarGoogle Scholar | open url image1

Wootton J (2002) Indirect effects in complex ecosystems: recent progress and future challenges. Journal of Sea Research 48, 157–172.
Crossref | GoogleScholarGoogle Scholar | open url image1

York RA, Battles JJ, Heald RC (2003) Edge effects in mixed conifer group selection openings: tree height response to resource gradients. Forest Ecology and Management 179, 107–121.
Crossref | GoogleScholarGoogle Scholar | open url image1