Seasonal soil and leaf CO 2 exchange rates in a Mediterranean holm oak forest and their responses to drought conditions

We measured the soil and leaf CO2 exchange in Quercus ilex and Phillyrea latifolia seasonally throughout the year in a representative site of the Mediterranean region, a natural holm oak forest growing in the Prades Mountains in southeastern Catalonia. In the wet seasons (spring and autumn), we experimentally decreased soil moisture by 30%, by excluding rainfall and water runoff in 12 plots, 1 10m, and left 12 further plots as controls. Our aim was to predict the response of these gas exchanges to the drought forecasted for the next decades for this region by GCM and ecophysiological models. Annual average soil CO2 exchange rate was 2.2770.27 mmolCO2m 2 s . Annual average leaf CO2 exchange rates were 871 and 571mmolm 2 s 1 in Q. ilex and P. latifolia, respectively. Soil respiration rates in control treatments followed a seasonal pattern similar to photosynthetic activity. They reached maximum values in spring and autumn (2.5–3.8 mmolm 2 s 1 soil CO2 emission rates and 7–15 mmolm 2 s 1 net photosynthetic rates) and minimum values (almost 0 for both variables) in summer, showing that soil moisture was the most important factor driving the soil microbial activity and the photosynthetic activity of plants. In autumn, drought treatment strongly decreased net photosynthesis rates and stomatal conductance of Q. ilex by 44% and 53%, respectively. Soil respiration was also reduced by 43% under drought treatment in the wet seasons. In summer there were larger soil CO2 emissions in drought plots than in control plots, probably driven by autotrophic (roots) metabolism. The results indicate that leaf and soil CO2 exchange may be strongly reduced (by ca. 44%) by the predicted decreases of soil water availability in the next decades. Long-term studies are needed to confirm these predictions or to find out possible acclimation of those processes. r 2006 Elsevier Ltd. All rights reserved.

[1]  P. Högberg,et al.  Natural abundance of 13C in CO2 respired from forest soils reveals speed of link between tree photosynthesis and root respiration , 2001, Oecologia.

[2]  A. Goldstein,et al.  Continuous measurements of soil respiration with and without roots in a ponderosa pine plantation in the Sierra Nevada Mountains , 2005 .

[3]  P. Bolstad,et al.  Annual soil respiration in broadleaf forests of northern Wisconsin: influence of moisture and site biological, chemical, and physical characteristics , 2005 .

[4]  J. Irvine,et al.  Coupling of canopy gas exchange with root and rhizosphere respiration in a semi-arid forest , 2005 .

[5]  L. Gratani,et al.  Adaptive photosynthetic strategies of the Mediterranean maquis species according to their origin , 2004, Photosynthetica.

[6]  M. G. Ryan,et al.  - 1 Interpreting , measuring , and modeling soil respiration , 2005 .

[7]  R. Conant,et al.  Controls on soil respiration in semiarid soils , 2004 .

[8]  Michael G. Ryan,et al.  Below-ground process responses to elevated CO2 and temperature: a discussion of observations, measurement methods, and models , 2004 .

[9]  N. McDowell,et al.  Response of the carbon isotopic content of ecosystem, leaf, and soil respiration to meteorological and physiological driving factors in a Pinus ponderosa ecosystem , 2004 .

[10]  J. Tenhunen,et al.  Factors influencing carbon fixation and water use by mediterranean sclerophyll shrubs during summer drought , 1990, Oecologia.

[11]  Hao-jie Xu,et al.  Deficiency of water can enhance root respiration rate of drought-sensitive but not drought-tolerant spring wheat , 2004 .

[12]  Josep Peñuelas,et al.  Comparative field study of Quercus ilex and Phillyrea latifolia: photosynthetic response to experimental drought conditions , 2003 .

[13]  S. Rambal,et al.  The key-role of topsoil moisture on CO2 efflux from a mediterranean Quercus ilex forest , 2003 .

[14]  Josep Peñuelas,et al.  Effect of drought on diameter increment of Quercus ilex, Phillyrea latifolia, and Arbutus unedo in a holm oak forest of NE Spain , 2003 .

[15]  J. Peñuelas,et al.  Comparative seasonal gas exchange and chlorophyll fluorescence of two dominant woody species in a Holm Oak Forest , 2003 .

[16]  E. Davidson,et al.  Effects of experimental drought on soil respiration and radiocarbon efflux from a temperate forest soil , 2002 .

[17]  M. Noguer,et al.  Climate change 2001: The scientific basis. Contribution of Working Group I to the Third Assessment Report of the Intergovernmental Panel on Climate Change , 2002 .

[18]  Anabel Sánchez,et al.  Likely effects of climate change on growth of Quercus ilex, Pinus halepensis, Pinus pinaster, Pinus sylvestris and Fagus sylvatica forests in the Mediterranean region , 2002 .

[19]  Josep Peñuelas,et al.  Severe Drought Effects on Mediterranean Woody Flora in Spain , 2001, Forest Science.

[20]  Charles T. Garten,et al.  Separating root and soil microbial contributions to soil respiration: A review of methods and observations , 2000 .

[21]  Jeffrey A. Andrews,et al.  Soil respiration and the global carbon cycle , 2000 .

[22]  W. Borken,et al.  A climate change scenario for carbon dioxide and dissolved organic carbon fluxes from a temperate forest soil: Drought and rewetting effects , 1999 .

[23]  J. Randerson,et al.  Primary production of the biosphere: integrating terrestrial and oceanic components , 1998, Science.

[24]  Josep Peñuelas,et al.  Comparative field study of spring and summer leaf gas exchange and photobiology of the mediterranean trees Quercus ilex and Phillyrea latifolia , 1998 .

[25]  J. Piñol,et al.  Carbon dioxide efflux and pCO2 in soils of threeQuercus ilex montane forests , 1995 .

[26]  M. Tretiach Photosynthesis and transpiration of evergreen Mediterranean and deciduous trees in an ecotone during a growing season , 1993 .

[27]  J. Brockwell,et al.  The natural abundance of , 1985 .

[28]  F. Cook,et al.  Relationship between soil respiration and soil moisture , 1983 .