Skip to main content

Carbon and Water Fluxes in Mediterranean-Type Ecosystems — Constraints and Adaptations

  • Chapter
Progress in Botany

Part of the book series: Progress in Botany ((BOTANY,volume 65))

Abstract

The regions with a climate of the Mediterranean-type have a rainy winter and a dry and hot summer. They are located on the western side of continents between latitudes 30 to 43° north or south (Walter 1973). The dry summer climate of Mediterranean regions arises from the seasonal change in position of the semi-permanent high-pressure zones that are centred over the tropical deserts at about 20° latitude north and south of the equator. The persistent flow of stable air out of these high-pressure centres during summer brings several months of hot, dry weather (Archibold 1995). This type of climate occurs in the Mediterranean Basin, California, on the western foot of the High Andes (Chile), the southwestern tip of Africa and southwestern Australia. In all these regions evergreen sclerophyllous woody plants are the dominant type of vegetation (Walter 1973), but high diversity of species and life forms is the rule. All the areas with Mediterranean endemics belong to the so-called hot-spots for biodiversity. Although the Mediterranean biome represents less than 2% of the world’s surface, it houses 20% of the world’s total floristic richness (Médail and Quézel 1997).

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

Access this chapter

Chapter
USD 29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 259.00
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD 329.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info
Hardcover Book
USD 329.99
Price excludes VAT (USA)
  • Durable hardcover edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

References

  • Archibold OW (1995) Ecology of world vegetation. Chapman and Hall, London

    Google Scholar 

  • Arco JM, Escudero A, Vega Garrido M (1991) Effects of site characteristics on nitrogen retranslocation from senescing leaves. Ecology 72:701–708

    Google Scholar 

  • Aschmann H (1973) Distribution and peculiarity of Mediterranean ecosystems. In: di Castri F, Mooney HA (eds) Mediterranean type ecosystems: origin and structure. Springer, Berlin Heidelberg New York, pp 11–19

    Google Scholar 

  • Atkin OK, Evans JR, Ball MC, Lambers H, Pons TL (2000) Leaf respiration of snow gum in the light and dark. Interactions between temperature and irradiance. Plant Physiol 122:915–923

    PubMed  CAS  Google Scholar 

  • Barrantes O, Fernández R, Joffre R, Ortega F (1986) Influencia del arbolado sobre el pasto en las dehesas. I Congresso Florestal Nacional, 2 a 6 de Dezembro 1986; Fundaçäo Calouste Gulbenkian, Lisboa, Portugal, pp 280–285

    Google Scholar 

  • Bellot J, Àvila A, Rodrigo A (1999) Throughfall and stemflow. In: Roda F, Retana J, Gracia CA, Bellot J (eds) Ecology of mediterranean evergreen oak forests. Springer, Berlin Heidelberg New York, pp 209–222

    Google Scholar 

  • Berry J, Björkman O (1980) Photosynthetic response and adaptation to temperature in higher plants. Annu Rev Plant Physiol 31:491–543

    Google Scholar 

  • Bertness MD, Callaway R (1994) Positive interactions in communities. TREE 9:191–193

    PubMed  CAS  Google Scholar 

  • Beyschlag W, Eckstein J (2001) Towards a causal analysis of stomatal patchiness: the role of stomatal size variability and hydrological heterogeneity. Act Oecol 22:161–173

    Google Scholar 

  • Beyschlag W, Pfanz H, Ryel RJ (1992) Stomatal patchiness in Mediterranean evergreen sclerophylls. Phenomenology and consequences for the interpretation of the midday depression in photosynthesis and transpiration. Planta 187:546–553

    Google Scholar 

  • Bilger W, Bjorkman O (1994) Relationships among violaxanthin deepoxidation, thylakoid membrane conformation, and nonphotochemical chlorophyll fluorescence quenching in leaves of cotton (Gossypium-Hirsutum L). Planta 193:238–246

    CAS  Google Scholar 

  • Blanco EM, González MAC, Tenorio MC, Bombin RE, Antón MG, Fuster MG, Manzaneque AG, Manzaneque FG, Saiz JCM, Juaristi CM, Pajares PR, Ollero HS (1997) Los bosques Ibéricos. Una interpretatión geobotánica. Planeta, Barcelona

    Google Scholar 

  • Breman H, Kessler JJ (1995) Woody plants in agro-ecosystems of semi-arid regions. Springer, Berlin Heidelberg New York

    Google Scholar 

  • Brooks JR, Meinzer FC, Coulombe R, Gregg J (2002) Hydraulic redistribution of soil water during summer drought in two contrasting Pacific Northwest coniferous forests. Tree Physiol 22:1107–1117

    PubMed  Google Scholar 

  • Buckley TN, Mott KA (2002) Stomatal water relations and the control of hydraulic supply and demand. Progress in botany 63. Springer, Berlin Heidelberg New York, pp 309–325

    Google Scholar 

  • Calabuig EL (1992) Bioclima. El Libro de las Dehesas Salamantinas. Junta de Castilla y León, Gráficas Ortega, Salamanca, Spain, pp 125–178

    Google Scholar 

  • Caldeira MC, Ryel RJ, Lawton JH, Pereira JS (2001) Mechanisms of positive biodiversity-production relationships: insights provided by 13C analysis in experimental Mediterranean grassland plots. Ecol Lett 4:439–443

    Google Scholar 

  • Caldwell MM, Richards JH (1989) Hydraulic lift-water efflux from upper roots improves effectiveness of water uptake by deep roots. Oecologia 79:1–5

    Google Scholar 

  • Canadell J, Jackson RB, Ehleringer JR, Mooney HA, Sala OE, Schulze ED (1996) Maximum rooting depth of vegetation types at the global scale. Oecologia 108:583–595

    Google Scholar 

  • Canadell J, Djema A, López B, Lloret F, Sabaté S, Siscart D, Gracia CA (1999) Structure and dynamics of the root system. In: Roda F, Retana J, Gracia CA, Bellot J (eds) Ecology of mediterranean evergreen oak forests. Springer, Berlin Heidelberg New York, pp 47–59

    Google Scholar 

  • Chaves MM (1991) Effects of water deficits on carbon assimilation. J Exp Bot 42:1–16

    CAS  Google Scholar 

  • Chaves MM, Pereira JS, Maroco JP, Rodrigues ML, Ricardo CPP, Osorio ML, Carvalho I, Faria T, Pinheiro C (2002) How plants cope with water stress in the field, photosynthesis and growth. Ann Bot 89:907–916

    PubMed  CAS  Google Scholar 

  • Chaves MM, Maroco JP, Pereira JS (2003) Carbon assimilation and growth under drought-from genes to the whole plant. Funct Plant Biol 30:1–26

    Google Scholar 

  • Cochard H, Breda N, Granier A (1996) Whole tree hydraulic conductance and water loss regulation in Quercus during drought: evidence for stomatal control of embolism? Ann Sci For 53:197–206

    Google Scholar 

  • Comín MP, Escarré A, Gracia CA, Lledó MJ, Rabella R, Savé R, Terradas J (1987) Water use by Quercus ilex L. in forests near Barcelona, Spain. In: Tenhunen JD, Catarino F, Lange OL, Oechel W (eds) Plant response to stress. Functional analysis in mediterranean ecosystems. Springer, Berlin Heidelberg New York, pp 259–266

    Google Scholar 

  • Correia MJ, Chaves MM, Pereira JS (1990) Afternoon depression in photosynthesis in grapevine leaves-evidence for a high light stress effect. J Exp Bot 41:417–426

    Google Scholar 

  • Correia MJ, Coelho D, David MM (2001) Response to seasonal drought in three cultivars of Ceratonia siliqua: leaf growth and water relations. Tree Physiol 21:645–653

    PubMed  CAS  Google Scholar 

  • Cowan IR (1982) Regulation of water use in relation to carbon gain in higher plants. In: Lange OL, Nobel PS, Osmond CB, Ziegler H (eds) Encyclopedia of plant physiology-physiological plant ecology II. Springer, Berlin Heidelberg New York, pp 589–613

    Google Scholar 

  • Cruiziat P, Cochard H, Ameglio T (2002) Hydraulic architecture of trees: main concepts and results. Ann For Sci 59:723–752

    Google Scholar 

  • Damesin C, Rambal S (1995) Field study of leaf photosynthetic performance by a Mediterranean deciduous oak tree (Quercus pubescens) during a severe summer drought. New Phytol 131:159–167

    Google Scholar 

  • David JS, Henriques MO, David TS, Tomé J, Ledger DC (1994) Clearcutting effects on streamflow in coppiced Eucalyptus globulus stands in Portugal. J Hydrol 162:143–154

    Google Scholar 

  • David TS (2000) Intercepção da precipitação e transpiração em árvores isoladas de Quercus rotundifolia Lam. (Rainfall interception and transpiration in isolated Quercus rotundifolia trees). Ph D, Universidade Técnica de Lisboa, Lisboa, Portugal

    Google Scholar 

  • David TS, Ferreira MI, David JS, Pereira JS (1997) Transpiration from a mature Eucalyptus globulus plantation in Portugal during a spring-summer period of progressively higher water deficit. Oecologia 110:153–159

    Google Scholar 

  • Davies WJ, Zhang J (1991) Root signals and the regulation of growth and development of plants in drying soil. Annu Rev Plant Physiol Plant Mol Biol 42:55–76

    CAS  Google Scholar 

  • Dawson TE (1993) Hydraulic lift and plant water use: implications for water balance, performance and plant-plant interactions. Oecologia 95:565–574

    Google Scholar 

  • Dawson TE (1996) Determining water use by trees and forests from isotopic, energy balance and transpiration analyses: the roles of tree size and hydraulic lift. Tree Physiol 16:263–272

    PubMed  Google Scholar 

  • Demmig-Adams B, Adams WW III (1992) Photoprotection and other responses of plants to high light stress. Annu Rev Plant Physiol Plant Mol Biol 43:599–626

    CAS  Google Scholar 

  • Demmig-Adams B, Adams WW III (1996) The role of xanthophyll cycle carotenoids in the protection of photosynthesis. Trends Plant Sci 1:21–26

    Google Scholar 

  • di Castri F (1981) Mediterranean-type shrublands of the world. In: di Castri F, Goodall DW, Specht RL (eds) Mediterranean-type shrublands. Elsevier, Amsterdam, pp 1–52

    Google Scholar 

  • Epron D, Dreyer E, Breda N (1992) Photosynthesis of oak trees [Quercus petraea (Matt.) Liebl.] during drought under field conditions: diurnal course of net CO2 assimilation and photochemical efficiency of photosystem II. Plant Cell Environ 15:809–820

    CAS  Google Scholar 

  • Escudero A, Arco JM, Sanz IC, Ayala J (1992) Effects of leaf longevity and retranslocation efficiency on the retention time of nutrients in the leaf biomass of different woody species. Oecologia 90:80–87

    Google Scholar 

  • Espigares T, Peco B (1995) Mediterranean annual pasture dynamics: impact of autumn drought. J Ecol 83:135–142

    Google Scholar 

  • Faria T, Garcia-Plazaola JI, Abadia A, Cerasoli S, Pereira JS, Chaves MM (1996) Diurnal changes in photoprotective mechanisms in leaves of cork oak (Quercus suber) during summer. Tree Physiol 16:115–123

    PubMed  Google Scholar 

  • Faria T, Silvério D, Breia E, Cabral R, Abadia A, Abadia J, Pereira JS, Chaves MM (1998) Differences in the response of carbon assimilation to summer stress (water deficits, high light and temperature) in four Mediterranean tree species. Physiol Plant 102:419–428

    CAS  Google Scholar 

  • Figueroa ME, Davy AJ (1991) Response of Mediterranean grassland species to changing rainfall. J Ecol 79:925–941

    Google Scholar 

  • Fuentes ER, Montenegro G, Rundel PW, Arroyo MTK, Ginocchio R, Jaksic FM (1995) Functional approaches to biodiversity in the Mediterranean-type ecosystems of central Chile. In: Davis GW, Richardson DM (eds) Mediterranean-type ecosystems-the function of biodiversity. Springer, Berlin Heidelberg New York, pp 185–232

    Google Scholar 

  • Genty B, Briantais JM, Da Silva JBV (1987) Effects of drought on primary photosynthetic processes of cotton leaves. Plant Physiol 83:360–364

    Google Scholar 

  • Gómez JA, Vanderliden K, Giráldez JV, Fereres E (2002) Rainfall concentration under olive trees. Agric Water Manage 55:53–70

    Google Scholar 

  • González-Bernaldez F, Morey M, Velasco F (1969) Influences of Quercus ilex on the herb layer at the El Prado forest (Madrid). A multivariate approach to community structure, diversity and environmental factors. Bol Real Soc Espaflola de Hist Nat (Biol) 67:265–284

    Google Scholar 

  • Gracia CA, Sabaté S, Martinez JM, Albeza E (1999) Functional responses to thinning. In: Roda F, Retana J, Gracia CA, Bellot J (eds) Ecology of mediterranean evergreen oak forests. Springer, Berlin Heidelberg New York, pp 329–338

    Google Scholar 

  • Hanson DT, Sharkey TD (2001) Effect of growth conditions on isoprene emission and other thermotolerance-enhancing compounds. Plant Cell Environ 24:929–936

    CAS  Google Scholar 

  • Harley PC, Tenhunen JD, Beyschlag W, Lange OL (1987) Seasonal changes in net photosynthesis rates and photosynthetic capacity in leaves of Cistus salvifolius, a European Mediterranean semi-deciduous shrub. Oecologia 74:380–388

    Google Scholar 

  • Hector A, Schmid B, Beierkuhnlein C, Caldeira MC, Diemer M, Dimitrakopoulos P, Finn JA, Freitas H, Giller PS, Good J, Harris R, Hochberg P, Huss-Danell K, Joshi J, Jumpponen A, Korner C, Leadley P, Loreau M, Minns A, Mulder CPH, O’Donovan G, Otway SJ, Pereira JS, Prinz A, Read DJ, Scherer-Lorenzen M, Schulze E-D, Siamantziouras A-SD, Spehn EM, Terry AC, Troumbis AY, Woodward FI, Yachi S, Lawton JH (1999) Plant diversity and productivity experiments in European grasslands. Science 286:1123–1127

    PubMed  CAS  Google Scholar 

  • Hobbs RJ, Mooney HA (1991) Effects of rainfall variability and gopher disturbance on serpentine annual grassland dynamics. Ecology 72:59–68

    Google Scholar 

  • Hobbs RJ, Richardson DM, Davis GW (1995) Mediterranean-type ecosystems: opportunities and constraints for studying the function of biodiversity. In: Davis GW, Richardson DM (eds) Mediterranean-type ecosystems-the function of biodiversity. Springer, Berlin Heidelberg New York, pp 1–42

    Google Scholar 

  • Hogg EH, Hurdle PA (1997) Sap flow in trembling aspen: implications for stomatal responses to vapor pressure deficit. Tree Physiol 17:501–509

    PubMed  Google Scholar 

  • Hulme M, Sheard N, Markham A (1999) Escenarios de cambio climático para la Península Ibérica. Climatic Research Unit, Norwich

    Google Scholar 

  • Infante JM, Rambal S, Joffre R (1997) Modelling transpiration in holm-oak savannah trees: scaling up from the leaf to the canopy. Agric For Meteorol 87:273–289

    Google Scholar 

  • Ishikawa CM, Bledsoe CS (2000) Seasonal and diurnal patterns of soil water potential in the rhizosphere of blue oaks: evidence of hydraulic lift. Oecologia 125:459–465

    Google Scholar 

  • Jackson LE (1985) Ecological origins of California’s mediterranean grasses. J Biogeogr 12:349–361

    Google Scholar 

  • Jackson PC, Meinzer FC, Bustamante M, Goldstein G, Franco A, Rundel PW, Caldas L, Igler E, Causin F (1999) Partitioning of soil water among tree species in a Brazilian Cerrado ecosystem. Tree Physiol 19:717–724

    PubMed  Google Scholar 

  • Jackson RB, Sperry JS, Dawson TE (2000) Root water uptake and transport: using physiological processes in global predictions. Trends Plant Sci 5:482–488

    PubMed  CAS  Google Scholar 

  • Jiménez MS, Cermák J, Kucera J, Morales D (1996) Laurel forests in Tenerife, Canary islands: the annual course of sap flow in Laurus trees and stand. J Hydrol 183:307–321

    Google Scholar 

  • Joffre R, los Llanos C (1986) Systèmes d’élevage et mise en valeur du milieu: étude des dehesas de la Sierra Norte de Seville. 10 Encontro sobre montados de sobro e azinho; 1986; Évora, Portugal, pp 193–214

    Google Scholar 

  • Joffre R, Rambal S (1988) Soil water improvement by trees in the rangelands of southern Spain. Act Oecol 9:405–422

    Google Scholar 

  • Joffre R, Rambal S (1993) How tree cover influences the water balance of Mediterranean rangelands. Ecology 74:570–582

    Google Scholar 

  • Jones HG, Sutherland RA (1991) Stomatal control of xylem embolism. Plant Cell Environ 14:607–612

    Google Scholar 

  • King BP, Harrison SJ (1998) Throughfall patterns under an isolated oak tree. Weather 53:111–121

    Google Scholar 

  • Ko LJ, Reich PB (1993) Oak trees effects on soil and herbaceous vegetation in savannas and pastures in Wisconsin. Am Midl Nat 130:31–42

    Google Scholar 

  • Kremer A, Roussel G (1982) Composantes de la croissance en hauteur chez le Pin maritime (Pinus pinaster Ait.). Ann Sci For 39:77–97

    Google Scholar 

  • Larcher W (2000) Temperature stress and survival ability of Mediterranean sclerophyllous plants. Plant Biosyst 134:279–295

    Google Scholar 

  • Lauenroth WK, Aguilera MO (1998) Plant-plant interactions in grasses and grasslands. In: Cheplick GP (ed) Population biology of grasses. Cambridge University Press, Cambridge, pp 209–230

    Google Scholar 

  • Leegood RC (1995) Effects of temperature on photosynthesis and photorespiration. In: Smirnoff N (ed) Environment and plant metabolism, flexibility and acclimation. Bioscientific, Oxford, pp 45–62

    Google Scholar 

  • Lemoine D, Peltier J-PGM (2001) Comparative studies of the water relations and the hydraulic characteristics in Fraxinus excelsior, Acer pseudoplatanus and A. opalus trees under soil water contrasted conditions. Ann For Sci 58:723–731

    Google Scholar 

  • Lewis DC (1968) Annual hydrologic response to watershed conversion from oak woodland to annual grassland. Water Resource Res 4:59–72

    Google Scholar 

  • Lloret F, Siscart D (1995) Los efectos demográficos de la sequía en poblaciones de encina. Cuad Soc Espanola Cienc For 2:77–81

    Google Scholar 

  • Llusia J, Penuelas J (2000) Seasonal patterns of terpene content and emission from seven Mediterranean woody species in field conditions. Am J Bot 87:133–140

    PubMed  CAS  Google Scholar 

  • Logan BA, Monson RK, Potosnak MJ (2000) Biochemistry and physiology of foliar isoprene production. Trends Plant Sci 5:477–481

    PubMed  CAS  Google Scholar 

  • Loreto F, Forster A, Durr M, Csiky O, Seufert G (1998) On the monoterpene emission under heat stress and on the increased thermotolerance of leaves of Quercus ilex L. fumigated with selected monoterpenes. Plant Cell Environ 21:101–107

    CAS  Google Scholar 

  • Loustau D, Berbigier P, Roumagnac P, Arruda-Pacheco C, David JS, Ferreira MI, Pereira JS, Tavares R (1996) Transpiration of a 64-year-old maritime pine stand in Portugal. 1. Seasonal course of water flux through maritime pine. Oecologia 107:33–42

    Google Scholar 

  • Marañon T (1985) Diversidad floristica y heterogeneidad ambiental en una dehesa de Sierra Morena. Anales de Edafologia y Agrobiologia, II. Biol Veg Agrobiol 44:1183–1197

    Google Scholar 

  • Marañon T (1986) Plant species richness and canopy effect in the savanna-like dehesa of SW Spain. Ecol Mediterranea 12:131–141

    Google Scholar 

  • Marañon T (1991) Diversidad en comunidades de pasto Mediterráneo: modelos y mecanismos de coexistencia. Ecologia 5:149–157

    Google Scholar 

  • Maroco JP, Breia E, Faria T, Pereira JS, Chaves MM (2002) Effects of long-term exposure to elevated CO2 sand N fertilization on the development of photosynthetic capacity and biomass accumulation in Quercus suber L. Plant Cell Environ 25:105–113

    Google Scholar 

  • Martinez F, Lazo YO, Fernandez-Galiano JM, Merino J (2002) Root respiration and associated costs in deciduous and evergreen species of Quercus. Plant Cell Environ 25:1271–1278

    Google Scholar 

  • Martinéz-Vilalta J, Prat E, Oliveras I, Piñol J (2002) Xylem hydraulic properties of roots and stems of nine Mediterranean woody species. Oecologia 133:19–29

    Google Scholar 

  • Médail F, Quézel P (1997) Hot-spots analysis for conservation of plant biodiversity in the Mediterranean Basin. Ann Mo Bot Gard 84:112–127

    Google Scholar 

  • Merino J (1987) The costs of growing leaves of Mediterranean plants. In: Tenhunen JD, Catarino F, Lange OL, Oechel W (eds) Plant response to stress. Functional analysis in mediterranean ecosystems. Springer, Berlin Heidelberg New York, pp 553–564

    Google Scholar 

  • Merino J, Field C, Mooney HA (1982) Construction and maintenance costs of Mediterranean-climate evergreen and deciduous leaves. I. Growth and CO2 carbon dioxide exchange analysis. Oecologia 53:208–213

    Google Scholar 

  • Merino J, Field C, Mooney HA (1984) Construction and maintenance costs of Mediterranean-climate evergreen and deciduous leaves. II. Biochemical pathway analysis. Act Oecol 5:211–229

    CAS  Google Scholar 

  • Miranda P, Coelho FES, Tome AR, Valente MA (2002) 20th century Portuguese climate and climate scenarios. In: Santos FD, Forbes K, Moita R (eds) Climate change in Portugal. Scenarios, impacts, and adaptation measures. Gradiva, Lisboa, Portugal, pp 25–83

    Google Scholar 

  • Mooney HA, Harrison AT, Morrow PA (1975) Environmental limitations of photosynthesis on a California evergreen shrub (Heteromeles arbutifolia). Oecologia 19:293–301

    Google Scholar 

  • Morgan JM (1984) Osmoregulation and water stress in higher plants. Annu Rev Plant Physiol Plant Mol Biol 35:299–319

    Google Scholar 

  • Myneni RB, Keeling CD, Tucker CJ, Asrar G, Nemani RR (1997) Increased plant growth in the northern high latitudes from 1981 to 1991. Nature 386:698–701

    CAS  Google Scholar 

  • Naeem S, Thompson LJ, Lawler SP, Lawton JH, Woodfin RM (1994) Declining biodiversity can alter the performance of ecosystems. Nature 368:734–737

    Google Scholar 

  • Nardini A, Tyree MT (1999) Root and shoot hydraulic conductance in Quercus species. Ann For Sci 56:371–377

    Google Scholar 

  • Nardini A, Lo Gullo MA, Salleo S (1999) Competitive strategies for water availability in two Mediterranean Quercus species. Plant Cell Environ 22:109–116

    Google Scholar 

  • Osborne CP, Chuine I, Viner D, Woodward FI (2000) Olive phenology as a sensitive indicator of future climatic warming in the Mediterranean. Plant Cell Environ 23:701–710

    Google Scholar 

  • Paulo M, Tavares M (1996) Policiclismo do crescimento do pinheiro bravo das dunas do litoral Portugues. Silva Lusitana 4:25–38

    Google Scholar 

  • Pereira JS, Tenhunen JD, Lange OL, Beyschlag W, Meyer A, David MM (1986) Seasonal and diurnal Patterns in leaf gas-exchange of Eucalyptus-globulus trees growing in Portugal. Can J For Res 16:177–184

    Google Scholar 

  • Pereira JS, Beyschlag G, Lange OL, Beyschlag W, Tenhunen JD (1987) Comparative phenology of four Mediterranean shrub species growing in Portugal. In: Tenhunen JD, Catarino FM, Lange OL, Oechel WC (eds) Plant response to stress. Springer, Berlin Heidelberg New York, pp 503–514

    Google Scholar 

  • Pereira JS, Correia AV, Correia AP, Branco M, Bugalho M, Caldeira MC, Souto-Cruz C, Freitas H, Oliveira AC, Pereira JMC, Reis RM, Vasconcelos MJ (2002) Forests and biodiversity. In: Santos FD, Forbes K, Moita R (eds) Climate change in Portugal. Scenarios, impacts and adaptation measures. Gradiva, Lisboa, Portugal, pp 363–414

    Google Scholar 

  • Perks MP, Irvine J, Grace J (2002) Canopy stomatal conductance and xylem sap abscisic acid (ABA) in mature Scots pine during a gradually imposed drought. Tree Physiol 22:877–884

    PubMed  CAS  Google Scholar 

  • Phillips JG, Riha SJ (1994) Root growth, water uptake and canopy development in Eucalyptus viminalis seedlings. Aust J Plant Physiol 21:69–78

    Google Scholar 

  • Pitt MD, Heady HF (1978) Responses of annual vegetation to temperature and rainfall patterns in northern California. Ecology 59:336–350

    Google Scholar 

  • Poole DK, Roberts SW, Miller PC (1981) Water utilization. In: Miller PC (ed) Resource use by chaparral and matorral. Springer, Berlin Heidelberg New York, pp 123–149

    Google Scholar 

  • Quick WP, Chaves MM, Wendler R, David M, Rodrigues ML, Passaharinho JA, Pereira JS, Adcock MD, Leegood RC, Stitt M (1992) The effect of water stress on photosynthetic carbon metabolism in four species grown under field conditions. Plant Cell Environ 15:25–35

    CAS  Google Scholar 

  • Rambal S (2001) Hierarchy and productivity of Mediterranean-type ecosystems. In: Roy J, Saugier B, Mooney HA (eds) Terrestrial global productivity. Academic Press, New York, pp 315–344

    Google Scholar 

  • Raven JA (2002) Selection pressures on stomatal evolution. New Phytol 153:371–386

    CAS  Google Scholar 

  • Reichstein M, Tenhunen JD, Roupsard O, Ourcival JM, Rambal S, Dore S, Valentini R (2002a) Ecosystem respiration in two Mediterranean evergreen Holm Oak forests: drought effects and decomposition dynamics. Funct Ecol 16:27–39

    Google Scholar 

  • Reichstein M, Tenhunen JD, Roupsard O, Ourcival JM, Rambal S, Miglietta F, Peressotti A, Pecchiari M, Tirone G, Valentini R (2002b) Severe drought effects on ecosystem CO2 and H2O fluxes at three Mediterranean evergreen sites: revision of current hypotheses? Global Change Biol 8:999–1017

    Google Scholar 

  • Roda F, Retana J, Gracia CA, Bellot J (1999) Ecology of Mediterranean oak forests. Springer, Berlin Heidelberg New York

    Google Scholar 

  • Rodrigues ML, Chaves MM, Wendler R, David MM, Quick WP, Leegood RC, Stitt M, Pereira JS (1993) Osmotic adjustment in water stressed grapevine leaves in relation to carbon assimilation. Aust J Plant Physiol 20:309–321

    CAS  Google Scholar 

  • Roy J (2001) How does biodiversity control primary productivity. In: Roy J, Saugier B, Mooney HA (eds) Terrestrial global productivity. Academic Press, San Diego, pp 169–186

    Google Scholar 

  • Sá CMMSS (2001) Influência do coberto arbóreo (Quercus suber L.) em processos ecofisiológicos da vegetação herbácea em áreas de montado. PhD, University of Évora, Évora, Portugal

    Google Scholar 

  • Sabaté S, Sala A, Gracia CA (1999) Leaf traits and canopy organization. In: Roda F, Retana J, Gracia CA, Bellot J (eds) Ecology of mediterranean oak forests. Springer, Berlin Heidelberg New York, pp 121–133

    Google Scholar 

  • Sala A (1999) Modelling canopy gas exchange during summer drought. In: Roda F, Retana J, Gracia CA, Bellot J (eds) Ecology of mediterranean oak forests. Springer, Berlin Heidelberg New York, pp 149–161

    Google Scholar 

  • Sala A, Tenhunen JD (1994) Site-specific water relations and stomatal response of Quercus ilex in a Mediterranean watershed. Tree Physiol 14:601–617

    PubMed  Google Scholar 

  • Salleo S, Nardini A, Pitt F, Lo Gullo MA (2000) Xylem cavitation and hydraulic control of stomatal conductance in Laurel (Laurus nobilis L.). Plant Cell Environ 23:71–79

    Google Scholar 

  • Schulze ED, Hall AE (1982) Stomatal responses, water loss and CO2 carbon dioxide assimilation rates of plants in contrasting environments. In: Lange OL, Nobel PS, Osmond CB, Ziegler H (eds) Encyclopedia of plant physiology-physiological plant ecology II. Springer, Berlin Heidelberg New York, pp 181–230

    Google Scholar 

  • Schulze ED, Caldwell MM, Canadell J, Mooney HA, Jackson RB, Parson D, Scholes R, Sala OE, Trimborn P (1998) Downward flux of water through roots (i.e. inverse hydraulic lift) in dry Kalahari sands. Oecologia 115:460–462

    Google Scholar 

  • Sharkey TD, Chen X, Yeh S (2001) Isoprene increases thermotolerance of fosmidomycin-fed leaves. Plant Physiol 125:2001–2006

    PubMed  CAS  Google Scholar 

  • Silva P, Nunes T, Campos C, Mariz M, Pio C (1999) Emissões de compostos orgânicos voláteis pela floresta de sobreiro em Portugal. 6th Conferência Nacional sobre a Qualidade do Ambiente; 1999 20 a 22 de Outubro; Lisboa, Portugal, pp 627–637

    Google Scholar 

  • Singsaas EL, Sharkey TD (2000) The effects of high temperature on isoprene synthesis in oak leaves. Plant Cell Environ 23:751–757

    CAS  Google Scholar 

  • Sperry JS (2000) Hydraulic constraints on plant gas exchange. Agric For Meteorol 104:13–23

    Google Scholar 

  • Staudt M, Mandl N, Joffre R, Rambal S (2001) Intraspecific variability of monoterpene composition emitted by Quercus ilex leaves. Can J For Res 31:174–180

    CAS  Google Scholar 

  • Sundby C, Melis A, Maenpaa P, Andersson B (1986) Temperature-dependent changes in the antenna size of photosystem-II-reversible conversion of photosystem-II-alpha to photosystem-II-Beta. Biochim Biophys Act 851:475–483

    CAS  Google Scholar 

  • Tardieu F, Simonneau T (1998) Variability among species of stomatal control under fluctuating soil water status and evaporative demand: modelling isohydric and anisohydric behaviours. J Exp Bot 49:419–432

    Google Scholar 

  • Tilman D (1997) Distinguishing between the effects of species diversity and species composition. Oikos 80:185

    Google Scholar 

  • Tognetti R, Longobucco A, Raschi A (1998) Vulnerability of xylem to embolism in relation to plant hydraulic resistance in Quercus pubescens and Quercus ilex co-occurring in a Mediterranean coppice stand in central Italy. New Phytol 139:437–447

    Google Scholar 

  • Tyree MT, Cochard H (1996) Summer and winter embolism in oak: impact on water relations. Ann Sci For 53:173–180

    Google Scholar 

  • Tyree MT, Sperry JS (1989) Vulnerability of xylem to cavitation and embolism. Annu Rev Plant Physiol Mol Biol 40:19–38

    Google Scholar 

  • Valente F, David JS, Gash JHC (1997) Modelling interception loss for two sparse eucalypt and pine forests in central Portugal using the reformulated Rutter and Gash analytical models. J Hydrol 190:141–162

    Google Scholar 

  • Valentini R, Matteucci G, Dolman AJ, Schulze ED, Rebmann C, Moors EJ, Granier A, Gross P, Jensen NO, Pilegaard K, Lindroth A, Grelle A, Bernhofer C, Grunwald T, Aubinet M, Ceulemans R, Kowalski AS, Vesala T, Rannik U, Berbigier P, Loustau D, Gudmundsson J, Thorgeirsson H, Ibrom A, Morgenstern K, Clement R, Moncrieff J, Montagnani L, Minerbi S, Jarvis PG (2000) Respiration as the main determinant of carbon balance in European forests. Nature 404:861–865

    PubMed  CAS  Google Scholar 

  • Verdaguer D, Casero P, Molinas M (2000) Lateral root development in a woody plant, Quercus suber L (cork oak). Can J Bot 78: 1125–1135

    Google Scholar 

  • Villar R, Merino J (2001) Comparison of leaf construction costs in woody species with differing leaf life-spans in contrasting ecosystems. New Phytol 151:213–226

    Google Scholar 

  • Walter H (1973) Vegetation of the earth. Springer, Berlin Heidelberg New York

    Google Scholar 

  • Werner C, Correia O, Beyschlag W (1999) Two different strategies of Mediterranean macchia plants to avoid photoinhibitory damage by excessive radiation levels during summer drought. Act Oecol 20:15–23

    Google Scholar 

  • Werner C, Ryel RJ, Correia O, Beyschlag W (2001) Effects of photoinhibition on whole-plant carbon gain assessed with a photosynthesis model. Plant Cell Environ 24:27–40

    CAS  Google Scholar 

  • Werner C, Correia O, Beyschlag W (2002) Characteristic patterns of chronic and dynamic photoinhibition of different functional groups in a Mediterranean ecosystem. Funct Plant Biol 29:999–1011

    Google Scholar 

  • White DA, Turner NC, Galbraith JH (2000) Leaf water relations and stomatal behavior of four allopatric Eucalyptus species planted in Mediterranean southwestern Australia. Tree Physiol 20:1157–1165

    PubMed  Google Scholar 

  • Wilkinson S, Davies WJ (2002) ABA-based chemical signalling: the co-ordination of responses to stress in plants. Plant Cell Environ 25:195–210

    PubMed  CAS  Google Scholar 

  • Wilson JR, Ludlow MM, Fisher MJ, Schulze ED (1980) Adaptation to water stress of the leaf water relations of four tropical forage species Panicum maximum var. trichoglume, Heteropogon contortus, Cenchrus ciliaris, Macroptilium atropurpureum. Aust J Plant Physiol 7:207–220

    Google Scholar 

  • Zimmermann MH (1983) Xylem structure and the ascent of sap. Springer, Berlin Heidelberg New York

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 2004 Springer-Verlag Berlin Heidelberg

About this chapter

Cite this chapter

Pereira, J.S., David, J.S., David, T.S., Caldeira, M.C., Chaves, M.M. (2004). Carbon and Water Fluxes in Mediterranean-Type Ecosystems — Constraints and Adaptations. In: Esser, K., Lüttge, U., Beyschlag, W., Murata, J. (eds) Progress in Botany. Progress in Botany, vol 65. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-18819-0_19

Download citation

  • DOI: https://doi.org/10.1007/978-3-642-18819-0_19

  • Publisher Name: Springer, Berlin, Heidelberg

  • Print ISBN: 978-3-642-62306-6

  • Online ISBN: 978-3-642-18819-0

  • eBook Packages: Springer Book Archive

Publish with us

Policies and ethics