Global change and root function

Global change includes land-use change, elevated CO2 concentrations, increased temperature and increased rainfall variability. All four aspects by themselves and in combination will influence the role of roots in linking below- and above-ground ecosystem function via organic and inorganic resource flows. Root-mediated ecosystem functions which may be modified by global change include below-ground resource (water, nutrients) capture, creation and exploitation of spatial heterogeneity, buffering of temporal variations in above-ground factors, supply and storage of C and nutrients to the below-ground ecosystem, mobilization of nutrients and C from stored soil reserves, and gas exchange between soil and atmosphere including the emission from soil of greenhouse gases. The theory of a functional equilibrium between root and shoot allocation is used to explore predicted responses to elevated CO2 in relation to water or nutrient supply as limiting root function. The theory predicts no change in root:shoot allocation where water uptake is the limiting root function, but substantial shifts where nutrient uptake is (or becomes) the limiting function. Root turnover will not likely be influenced by elevated CO2, but by changes in regularity of water supply. A number of possible mechanisms for root-mediated N mineralization is discussed in the light of climate change factors. Rhizovory (root consumption) may increase under global change as the balance between plant chemical defense and adapted root consuming organisms may be modified during biome shifts in response to climate change. Root-mediated gas exchange allows oxygen to penetrate into soils and methane (CH4) to escape from wetland soils of tundra ecosystems as well as tropical rice production systems. The effect on net greenhouse gas emissions of biome shifts (fens replacing bogs) as well as of agricultural land management will depend partly on aerenchyma in roots.

[1]  Pete Smith,et al.  Global change, soil biodiversity, and nitrogen cycling in terrestrial ecosystems: three case studies , 1998 .

[2]  J. Ingram,et al.  The interaction of soil biota and soil structure under global change , 1998 .

[3]  B. Griffiths,et al.  Effect of elevated CO2 on rhizosphere carbon flow and soil microbial processes , 1997 .

[4]  K. Stephen,et al.  Oxidation of methane in peat: Kinetics of CH4 and O2 removal and the role of plant roots , 1997 .

[5]  M. Schortemeyer,et al.  Soil microbial responses to increased concentrations of atmospheric CO2 , 1997 .

[6]  S. C. Geijn,et al.  Carbon balance and water use efficiency of frequently cut Lolium perenne L. swards at elevated carbon dioxide , 1997 .

[7]  B. D. Campbell,et al.  Elevated CO 2and water supply interactions in grasslands: a pastures and rangelands management perspective , 1997 .

[8]  Hannu Nykänen,et al.  Fluxes of nitrous oxide from boreal peatlands as affected by peatland type, water table level and nitrification capacity , 1996 .

[9]  I. Stulen,et al.  Modulation of carbon and nitrogen allocation in Urtica dioica and Plantago major by elevated CO2: Impact of accumulation of nonstructural carbohydrates and ontogenetic drift. , 1996 .

[10]  P. Coley,et al.  Anti-Herbivore Defenses of Young Tropical Leaves: Physiological Constraints and Ecological Trade-offs , 1996 .

[11]  C. Rouland,et al.  Foraging, nesting and damage caused by Microtermes subhyalinus (Isoptera: Termitidae) in a sugarcane plantation in the Central African Republic , 1996 .

[12]  I. Stulen,et al.  The response of Plantago major ssp pleiosperma to elevated CO2 is modulated by the formation of secondary shoots , 1996 .

[13]  J. Bubier The Relationship of Vegetation to Methane Emission and Hydrochemical Gradients in Northern Peatlands , 1995 .

[14]  P. Martikainen,et al.  Emissions of CH4, N20 and CO2 from a virgin fen and a fen drained for grassland in Finland , 1995 .

[15]  J. Schimel Plant transport and methane production as controls on methane flux from arctic wet meadow tundra , 1995 .

[16]  P. Martikainen,et al.  Effect of a lowered water table on nitrous oxide fluxes from northern peatlands , 1993, Nature.

[17]  J. P. Grime,et al.  Evidence of a feedback mechanism limiting plant response to elevated carbon dioxide , 1993, Nature.

[18]  M. Noordwijk,et al.  Concepts and methods for studying interactions of roots and soil structure , 1993 .

[19]  W. H. van der Putten,et al.  Plant-specific soil-borne diseases contribute to succession in foredune vegetation , 1993, Nature.

[20]  H. Rogers,et al.  Cotton root and rhizosphere responses to free‐air CO2 enrichment , 1992 .

[21]  C. Körner,et al.  Responses to elevated carbon dioxide in artificial tropical ecosystems. , 1992, Science.

[22]  H. Rogers,et al.  Response of plant roots to elevated atmospheric carbon dioxide , 1992 .

[23]  L. Lekkerkerk,et al.  Carbon Fluxes in Plant-Soil Systems at Elevated Atmospheric CO2 Levels. , 1991, Ecological applications : a publication of the Ecological Society of America.

[24]  R. Cowie,et al.  Termite (Isoptera) control in agriculture and forestry by non-chemical methods: a review. , 1990 .

[25]  R. Norby Nodulation and nitrogenase activity in nitrogen-fixing woody plants stimulated by CO2 enrichment of the atmosphere , 1987 .

[26]  R. Norby,et al.  Increases in mycorrhizal colonization and seedling growth in Pinusechinata and Quercusalba in an enriched CO2 atmosphere , 1987 .

[27]  Eric S. Menges,et al.  Patterns of Change in the Carbon Balance of Organic Soil-Wetlands of the Temperate Zone , 1986 .

[28]  J. Whipps Effect of CO2 Concentration on Growth, Carbon Distribution and Loss of Carbon from the Roots of Maize , 1985 .

[29]  H. Lambers THE FUNCTIONAL EQUILIBRIUM, NIBBLING ON THE EDGES OF A PARADIGM , 1983 .

[30]  James F. Reynolds,et al.  A Shoot:Root Partitioning Model , 1982 .

[31]  F. S. Chapin,et al.  The Mineral Nutrition of Wild Plants , 1980 .

[32]  F. Jones,et al.  The soil as an environment for plant parasitic nematodes , 1975 .

[33]  D. Janzen Herbivores and the Number of Tree Species in Tropical Forests , 1970, The American Naturalist.

[34]  H. Mooney,et al.  20 – Stimulation of Global Photosynthetic Carbon Influx by an Increase in Atmospheric Carbon Dioxide Concentration , 1996 .

[35]  H. Mooney,et al.  1 – Tree Responses to Elevated CO2 and Implications for Forests , 1996 .

[36]  Basil Acock,et al.  19 – Progress, Limitations, and Challenges in Modeling the Effects of Elevated CO2 on Plants and Ecosystems , 1996 .

[37]  H. Mooney,et al.  3 – Linking Above- and Belowground Responses to Rising CO2 in Northern Deciduous Forest Species , 1996 .

[38]  H. Mooney,et al.  5 – Growth Strategy and Tree Response to Elevated CO2: A Comparison of Beech (Fagus sylvatica) and Sweet Chestnut (Castanea sativa Mill.) , 1996 .

[39]  G. Koch,et al.  21 – Biota Growth Factor β: Stimulation of Terrestrial Ecosystem Net Primary Production by Elevated Atmospheric CO2 , 1996 .

[40]  Robert L. Sanford,et al.  Root Growth and Rhizosphere Interactions in Tropical Forests , 1996 .

[41]  S V Krupa,et al.  Plant responses to atmospheric CO2 enrichment with emphasis on roots and the rhizosphere. , 1994, Environmental pollution.

[42]  C. Andersen,et al.  Mycorrhizae alter quality and quantity of carbon allocated below ground , 1994, Nature.

[43]  F. Stuart Chapin,et al.  Environmental and biotic controls over methane flux from Arctic tundra , 1993 .

[44]  J. G. Buwalda,et al.  The carbon costs of root systems of perennial fruit crops , 1993 .

[45]  F. A. Bazzaz,et al.  The Response of Natural Ecosystems to the Rising Global CO2 Levels , 1990 .

[46]  P. Lavelle,et al.  Soil ingestion and growth in Millsonia anomala, a tropical earthworm, as influenced by the quality of the organic matter ingested , 1989, Pedobiologia.

[47]  M. van Noordwijk,et al.  Agricultural concepts of roots: from morphogenetic to functional equilibrium between root and shoot growth , 1987 .

[48]  D. Pimentel Biological Invasions of Plants and Animals in Agriculture and Forestry , 1986 .

[49]  B. Veen Energy cost of ion transport. , 1979, Basic life sciences.