Abstract
Mediterranean-type climates are characterized by warm or hot summers, mild or cold winters and, especially, by the existence of a summer drought period driven by the low or even nule precipitation during this season. Mediterranean-type climates are represented in different areas of the world, both in the Northern and the Southern Hemisphere . Specifically, regarding the existence of Quercus under these climatic conditions, two main geographical areas should be considered, namely the Mediterranean Basin in the Palearctic and California (USA) and Baja California (Mexico) in the Nearctic. Despite the relatively low geographical extension of the areas occupied by oaks under this type of climate, it has deserved its own phytoclimatical entity since the first geobotanical synthesis at a global scale. Although evergreen and sclerophyllous oak species are widely assumed as a prototype of mediterranean oaks, both palaeoecological evidences and present biogeographical analysis confirm the co-existence of this oak type with winter -deciduous species of the same genus. In this chapter, the different advantages and disadvantages of both phenological patterns (evergreeness and winter -deciduousness) are presented. Moreover, the strategies for saving water through the overall leaf size reduction, the stomatal control of water losses or some xeromorphic traits for a further reduction of transpiration are also shown. Finally, the development of a high resistance to drought -induced cavitation , as a way for co** with low water potential during dry periods, is discussed.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Similar content being viewed by others
References
Abadía A, Gil E, Morales F, Montañés L, Montserrat G, Abadía J (1996) Marcescence and senescence in a submediterranean oak (Quercus subpyrenaica E.H. del Villar): photosynthetic characteristics and nutrient composition. Plant, Cell Environ 19:685–694
Acherar M, Rambal S (1992) Comparative relations of four Mediterranean oak species. Vegetatio 99–100:177–184
Ackerly DD, Knight CA, Weiss SB, Barton K, Starmer KP (2002) Leaf size, specific leaf area and microhabitat distribution of woody plants in a California chaparral: contrasting patterns in species level and community level analyses. Oecologia 130:449–457
Ackerly DD (2004) Adaptation, niche conservatism, and convergence: comparative studies of leaf evolution in the California chaparral. Am Nat 163:654–671
Ackerly DD (2009) Evolution, origin and age of lineages in the Californian and Mediterranean floras. J Biogeogr 36:1221–1233
Andivia E, Carevic F, Fernández M, Alejano R, Vázquez-Piqué J, Tapias R (2012) Seasonal evolution of water status after outplanting of two provenances of Holm oak nursery seedlings. New For 43:815–824
Aranwela N, Sanson G, Read J (1999) Methods of assessing leaf-fracture properties. New Phytol 144:369–393
Archibold OW (1995) Ecology of world vegetation. Chapman & Hall, London
Arizaga S, Martínez-Cruz J Salcedo-Cabrales M, Bello-González MA (2009) Manual de la biodiversidad de encinos michoacanos. Semarnat, INE, Mexico
Atjay GL, Ketner P, Duvigneaud P (1979) Terrestrial primary production and phytomass. In: Bolin B, Degens ET, Kempe S, Ketner P (eds) The global carbon cycle, SCOPE Report 13. Wiley, UK, pp 129–181
Axelrod DI (1973) History of the Mediterranean ecosystem in California. In: Di Castri F, Mooney HA (eds) Mediterranean type ecosystems. Origin and structure. Springer, Berlin, pp 225–277
Axelrod DI (1975) Evolution and biogeography of Madrean-Tethyan sclerophyll vegetation. Ann Mo Bot Gar 62:280–334
Axelrod DI (1977) Outline history of California vegetation. In: Barbour MG, Major J (eds) Terrestrial vegetation of California. John Wiley, New York, pp 139–193
Axelrod DI (1989) Age and origin of Chaparral. The California Chaparral: paradigms revisited (ed. SC Keeley) Natural History Museum of Los Angeles County, Los Angeles, pp 7–19
Baldocchi DD, Xu L (2007) What limits evaporation from Mediterranean oak woodlands—the supply of moisture in the soil, physiological control by plants or the demand by the atmosphere? Adv Water Resour 30:2113–2122
Baldocchi DD, Ma S, Rambal S, Misson L, Ourcival JM, Limousin JM, Papale D (2010) On the differential advantages of evergreenness and deciduousness in Mediterranean oak woodlands: a flux perspective. Ecol Appl 20:1583–1597
Barbero M, Loisel R, Quèzel P (1992) Biogeography, ecology and history of Mediterranean Quercus ilex ecosystems. Vegetatio 99–100:19–34
Barbosa M, Fernandes GW (2014) Bottom-up effects on gall distribution. In: Fernandes GW, Santos JC (eds) Neotropical insect galls. Springer, Dordrecht, pp 99–113
Barbour MG (1988) Californian upland forests and woodlands. In: Barbour MG, Billings WD (eds) North American terrestrial vegetation. Cambridge University Press, Cambridge, pp 131–164
Barbour MG, Minnich RH (1990) The myth of chaparral convergence. Israel J Bot 39:453–463
Beadle NCW (1953) The edaphic factor in plant ecology with a special note on soil phosphates. Ecology 34:426–428
Beadle NCW (1954) Soil phosphate and the delimitation of plant communities in eastern Australia. Ecology 35:370–375
Beadle NCW (1966) Soil phosphate and its role in molding segments of the Australian flora and vegetation, with special reference to xeromorphy and sclerophylly. Ecology 47:992–1007
Benz BW, Martin CE (2006) Foliar trichomes, boundary layers, and gas exchange in 12 species of epiphytic Tillandsia (Bromeliaceae). J Plant Physiol 163:648–656
Bernays EA (1981) Plant tannins and insect herbivores: an appraisal. Ecol Entomol 6:353–360
Bethoux JP, Gentili B, Morin P, Nicolas E, Pierre C, Ruiz-Pino D (1999) The Mediterranean Sea: a miniature ocean for climatic and environmental studies and a key for climatic functioning of the North Atlantic. Prog Oceanogr 44:131–146
Bhaskar R, Ackerley DD (2006) Ecological relevance of minimum seasonal water potentials. Physiol Plant 127:353–359
Bhaskar R, Valiente-Banuet A, Ackerly DD (2007) Evolution of hydraulic traits in closely related species pairs from mediterranean and non-mediterranean environments of North America. New Phytol 176:718–726
Bickford CP (2016) Ecophysiology of leaf trichomes. Funct Plant Biol 43:807–814
Blackman CJ, Brodribb TJ, Jordan GJ (2010) Leaf hydraulic vulnerability is related to conduit dimensions and drought resistance across a diverse range of woody angiosperms. New Phytol 188:1113–1123
Blondel J, Aronson J (1995) Biodiversity and ecosystem function in the Mediterranean Basin: human and nonhuman determinants. In: Davis GW, Richardson DM (eds) Mediterranean-type ecosystems: the function of biodiversity. Springer, Berlin, pp 43–119
Blumler MA (1991) Winter-deciduous versus evergreen habit in Mediterranean regions: a model. USDA Forest Service Gen Tech Rep PSW-126
Blumler MA (2005) Three conflated definitions of Mediterranean climates. Middle States Geographer 38:52–60
Bozzano M, Turok J (2003) Mediterranean Oaks network, report of the second meeting, 2–4 may 2002-Gozo. Malta, International Plant Genetics Resources Institute, Rome, Italy
Breckle SW (2002) Walter’s vegetation of the earth. The ecological systems of the geo-biosphere. 4th edn. Springer, Berlin
Brewer CA, Smith WK (1997) Patterns of leaf surface wetness for montane and subalpine plants. Plant, Cell Environ 20:1–11
Brodribb TJ, Holbrook NM, Edwards EJ, Gutierrez MV (2003) Relations between stomatal closure, leaf turgor and xylem vulnerability in eight tropical dry forest trees. Plant, Cell Environ 26:443–450
Bryson RA, Hare FK (1974) Climates of North America. World Survey of Climatology, vol 11. Elsevier Scientific Publishing Co., Amsterdam
Büntgen U, Tegel W, Nicolussi K, McCormick M, Frank D, Trouet V, Kaplan JO, Franz Herzig F, Heussner KU, Wanner H, Luterbacher J, Esper J (2011) 2500 years of European climate variability and human susceptibility. Science 33:578–582
Burghardt M, Riederer M (2003) Ecophysiological relevance of cuticular transpiration of deciduous and evergreen plants in relation to stomatal closure and leaf water potential. J Exp Bot 54:1941–1949
Bussotti F, Bettini D, Grossoni P, Mansuino S, Nibbi R, Soda C, Tani C (2002) Structural and functional traits of Quercus ilex in response to water availability. Environ Exp Bot 47:11–23
Bussotti F, Ferrini F, Pollastrini M, Alessio Fini A (2014) The challenge of Mediterranean sclerophyllous vegetation underclimate change: from acclimation to adaptation. Environ Exp Bot 103:80–98
Castro-Díez P, Pedro Villar-Salvador P, Pérez-Rontomé C, Maestro-Martínez M Montserrat-Martí G (1997) Leaf morphology and leaf chemical composition in three Quercus (Fagaceae) species along a rainfall gradient in NE Spain. Trees 11:127–134
Castro-Díez P, Montserrat-Martí G (1998) Phenological pattern of fifteen Mediterranean phanaerophytes from Quercus ilex communities of NE-Spain. Plant Ecol 139:103–112
Cavender-Bares J, Kitajima K, Bazzaz FA (2004) Multiple trait associations in relation to habitat differentiation among 17 Floridian oak species. Ecol Monogr 74:635–662
Chabot BF, Hicks DJ (1982) The ecology of leaf life spans. Annu Rev Ecol Syst 13:229–259
Christman MA, Sperry JS, Smith DD (2012) Rare pits, large vessels and extreme vulnerability to cavitation in a ring-porous tree species. New Phytol 193:713–720
Choat B, Jansen S, Brodribb TJ, Cochard H, Delzon S, Bhaskar R, Bucci SJ, Feild TS, Gleason SM, Hacke UG, Jacobsen AL, Lens F, Maherali H, Martínez-Vilalta J, Mayr S, Mencuccini M, Mitchell PJ, Nardini A, Pittermann J, Pratt RB, Sperry JS, Westoby M, Wright IJ, Zanne AE (2012) Global convergence in the vulnerability of forests to drought. Nature 491:752–755
Choong MF, Lucas PW, Ong JSY, Pereira B, Tan HTW, Turner IM (1992) Leaf fracture toughness and sclerophylly: their correlations and ecological implications. New Phytol 121:597–610
Cody ML, Mooney HA (1978) Convergence versus nonconvergence in Mediterranean-Climate ecosystems. Annu Rev Ecol Syst 9:265–321
Cochard H, Breda N, Granier A, Aussenac G (1992) Vulnerability to air-embolism of 3 European oak species (Quercus petraea (Matt) Liebl, Quercus pubescens Willd, L). Ann Sci For 49:225–233
Cochard H, Tyree MT (1990) Xylem dysfunction in Quercus: vessel sizes, tyloses, cavitation and seasonal changes in embolism. Tree Physiol 6:393–407
Corcuera L, Camarero JJ, Gil-Pelegrín E (2002) Functional groups in Quercus species derived from the analysis of pressure-volume curves. Trees 16:465–472
Corcuera L, Camarero JJ, Gil-Pelegrín E (2004a) Effects of a severe drought on Quercus ilex radial growth and xylem anatomy. Trees 18:83–92
Corcuera L, Camarero JJ, Gil-Pelegrín E (2004b) Effects of a severe drought on growth and wood anatomical properties of Quercus faginea. IAWA J 25:185–204
Corcuera L, Morales F, Abadía A, Gil-Pelegrín E (2005a) The effect of low temperatures on the photosynthetic apparatus of Quercus ilex subsp. ballota at its lower and upper altitudinal limits in the Iberian peninsula and during a single freezing-thawing cycle. Trees 19:99–108
Corcuera L, Morales F, Abadía A, Gil-Pelegrín E (2005b) Seasonal changes in photosynthesis and photoprotection in a Quercus ilex subsp. ballota woodland located in its upper altitudinal extreme in the Iberian Peninsula. Tree Physiol 25:599–608
Corcuera L, Camarero JJ, Sisó S, Gil-Pelegrín E (2006) Radial-growth and wood-anatomical changes in overaged Quercus pyrenaica coppice stands: functional responses in a new Mediterranean landscape. Trees 20:91–98
Cowling RM, Campbell BM (1983) The definition of leaf consistence categories in the fynbos biome and their distribution along an altitudinal gradient in the south eastern Cape. J S Afr Bot 49:87–101
Cowling RM, Witkowski ETF (1994) Convergence and non-convergence of plant traits in climatically and edaphically matched sites in Mediterranean Australia and South Africa. Aust J Ecol 19:220–232
Cowling RM, Rundel PW, Lamont BB, Arroyo MK, Arianoutsou M (1996) Plant diversity in mediterranean-climate regions. Trends Ecol Evol 11:362–366
Cuadrat JM, Saz MA, Vicente-Serrano S, González-Hidalgo JC (2007) Water resources and precipitation trends in Aragon (Spain). Int J Water Resour D 23:107–124
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
Damesin C, Rambal S, Joffre R (1998) Co-occurrence of trees with different leaf habit: a functional approach on Mediterranean oaks. Acta Oecol 19:195–204
David TS, Henriques MO, Kurz-Besson C, Nunes J, Valente F, Vaz M, Pereira JS, Siegwolf R, Chaves MM, Gazarini LC, David JS (2007) Water-use strategies in two co-occurring Mediterranean evergreen oaks: surviving the summer drought. Tree Physiol 27:793–803
Deitch MJ, Sapundjieff MJ, Feirer ST (2017) Characterizing precipitation variability and trends in the world’s Mediterranean-Climate areas. Water 9:259
del Río S, Penas A (2006) Potential distribution of semi-deciduous forests in Castile and Leon (Spain) in relation to climatic variations. Plant Ecol 185:269–282
Denk T, Grimm GW (2009) Significance of pollen characteristics for infrageneric classification and phyllogeny in Quercus (Fagaceae). Int J Plant Sci 170(7):926–940
Ding Y, Zhang Y, Zheng QS, Tyree MT (2014) Pressure-volume curves: revisiting the impact of negative turgor during cell collapse by literature review and simulations of cell micromechanics. New Phytol 203:378–387
Di Paola A, Paquette A, Trabucco A, Mereu S, Valentini R, Paparella F (2017) Coexistence trend contingent to Mediterranean oaks with different leaf habits. Ecol Evol 7:3006–3015
Dolph GE, Dilcher DL (1980) Variation in leaf size with respect to climate in the tropics of the Western-hemisphere. Bull Torrey Bot Club 107:154–162
Dreyer E, Le Roux X, Montpied P, Duadet FA, Masson F (2001) Temperature response of leaf photosynthetic capacity in seedlings from seven temperate tree species. Tree Physiol 21:223–232
Dufour-Dror JM, Ertas (2004) A Bioclimatic perspectives in the distribution of Quercus ithaburensis Decne. Subspecies in Turkey and in the Levant. J Biogeogr 31:461–474
Edwards C, Read J, Sanson G (2000) Characterising sclerophylly: some mechanical properties of leaves from heath and forest. Oecologia 123:158–167
Ehleringer J (1981) Leaf absorptances of Mohave and Sonoran desert plants. Oecologia 49:366–370
Ehleringer J, Björkman O, Mooney HA (1976) Leaf pubescence: effects on absorptance and photosynthesis in a desert shrub. Science 192:376–377
Ehleringer J, Björkman O (1978) Pubescence and leaf spectral characteristics in a desert shrub, Encelia farinosa. Oecologia 36:151–162
Ehleringer J, Mooney HA, Gulmon SL, Rundel PW (1981) Parallel evolution of leaf pubescence in Encelia in coastal deserts of north and south America. Oecologia 49:38–41
Ehleringer J (1984) Ecology and ecophysiology of leaf pubescence in North American desert plants. In: Rodriguez E, Healey PL, Mehta I (eds) Biology and chemistry of plant trichomes. Plenum, New York, pp 113–132
Ehleringer J, Mooney HA (1978) Leaf hairs: effects on physiological activity and adaptive value to a desert shrub. Oecologia 37:183–200
Ehleringer JR, Smedly MP (1988) Stomatal sensitivity and water-use efficiency in oaks and their hybrids. In: Wallace A, McArthur ED, Haferkamp MR (eds) Symposium on shrub ecophysiology and biotechnology. USDA Forest Service Tech Rep INT-256, Ogden, UT, pp 98–102
Ehleringer JR, Phillips SL (1996) Ecophysiological factors contributing to the distributions of several Quercus species in the Intermountain West. Ann Sci Forest 53:291–302
Epron D, Dreyer E (1992) Effects of severe dehydration on leaf photosynthesis in Quercus petraea (Matt.) Liebl.: photosystem II efficiency, photochemical and non-photochemical fluorescence quenching and electrolyte leakage. Tree Physiol 10:273–284
Epron D, Dreyer E (1993) Long-term effects of drought on photosynthesis of adult oak trees (Quercus petraea Matt.) Liebl. and Quercus robur L.) in a natural stand. New Phytol 125:381–389
Escudero A, Mediavilla S (2003) Decline in photosynthetic nitrogen use efficiency with leaf age and nitrogen resorption as determinants of leaf life span. J Ecol 91:880–889
Esteso-Martínez J, Camarero JJ, Gil-Pelegrín E (2006) Competitive effects of herbs on Quercus faginea seedlings inferred from vulnerability curves and spatial-pattern analyses in a Mediterranean stand (Iberian System, northeastern Spain). Ecoscience 13(3):378–387
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
Farrant JM (2000) A comparison of mechanisms of desiccation tolerance among three angiosperm resurrection plant species. Plant Ecol 151:29–39
Feeny P (1970) Seasonal changes in oak leaf tannins and nutrients as a cause of spring feeding by winter moth caterpillars. Ecology 51:565–581
Felger RS, Johnson MB, Wilson MF (2001) The trees of Sonora. Oxford University Press, Oxford, Mexico
Fernández V, Sancho-Knapik, Guzmán P, Peguero-Pina JJ, Gil L, Karabourniotis G, Khayet M, Fasseas C, Heredia-Guerrero JA, Heredia A, Gil-Pelegrín E (2014) Wettability, polarity, and water absorption of holm oak leaves: effect of leaf side and age. Plant Physiol 166:168–180
Fick SE, Hijmans RJ (2017). WorldClim 2: new 1-km spatial resolution climate surfaces for global land areas. Int J Climatol doi:10.1002/joc.5086
Filella I, Llusià J, Piñol J, Peñuelas J (1998) Leaf gas exchange and fluorescence of Phillyrea latifolia, Pistacia lentiscus and Quercus ilex saplings in severe drought and high temperature conditions. Environ Exp Bot 39:213–220
Flexas J, Diaz-Espejo A, Gago J, Gallé A, Galmés J, Gulías J, Medrano H (2014) Photosynthetic limitations in Mediterranean plants: A review. Environ Exp Bot 103:12–23
Follieri M, Magri D, Sadori L (1988) 250,000-year pollen record from Valle di Castigliore (Roma). Pollen Spores 30:329–356
Fonseca CR, Overton JM, Collins B, Westoby M (2000) Shifts in trait-combinations along rainfall and phosphorus gradients. J Ecol 88:964–977
Fotelli MN, Radoglou M, Constantinidou H-IA (2000) Water stress responses of seedlings of four Mediterranean oak species. Tree Physiol 20:1065–1075
Fralish JS, Franklin SB (2002) Taxonomy and ecology of woody plants in North American forests (excluding Mexico and Subtropical Florida). Wiley, New York
Franks PJ, Beerling DJ (2009) Maximun leaf conductance driven by CO2 effects on stomatal size and density over geologic time. PNAS 106:10343–10347
Frisch HL (1991) Fundamentals of membrane transport. Polym J 23:445–456
Galmés J, Medrano H, Flexas J (2007) Photosynthesis and photoinhibition in response to drought in a pubescent (var. minor) and a glabrous (var. palaui) variety of Digitalis minor. Environ Exp Bot 60:105–111
García-Ruiz JM, López-Moreno JI, Vicente-Serrano SM, Lasanta T, Beguería S (2011) Mediterranean water resources in a global change scenario. Earth Sci Rev 105:121–139
García-Ruiz JM, Nadal-Romero E, Lana-Renault N, Beguería S (2013) Erosion in Mediterranean landscapes: changes and future challenges. Geomorphology 198:20–36
García-Plazaola JI, Artetxe U, Duñabeitia MK, Becerril JM (1999) Role of photoprotective systems of Holm-Oak (Quercus ilex) in the adaptation to winter conditions. J Physiol 155:25–630
Gasith A, Resh VH (1999) Streams in Mediterranean climate regions: abiotic influences and biotic responses to predictable seasonal events. Annu Rev Ecol Syst 30:51–81
Gibson AC (1998) Photosynthetic organs of desert plants. Bioscience 48:911–920
Giertych MJ, Karolewski P, Oleksyn J (2015) Carbon allocation in seedlings of deciduous tree species depends on their shade tolerance. Acta Physiol Plant 37:216
Gil-Pelegrín E, Peguero-Pina JJ, Camarero JJ, Fernández-Cancio A, Navarro-Cerrillo R (2008) Drought and forest decline in the Iberian Peninsula: a simple explanation for a complex phenomenom? In: Sánchez JM (ed) Droughts: causes, effects and predictions. Nova Science Publishers Inc., New York, pp 27–68
Givnish T (1976) Leaf form in relation to environment: a theoretical study. PhD Thesis, Princeton University
Givnish TJ (1987) Comparative studies of leaf form: assessing the relative roles of selective pressures and phylogenetic constraints. New Phytol 106:131–160
Givnish TJ (2002) Adaptive significance of evergreen versus deciduous leaves: solving the triple paradox. Silva Fenn 36:703–743
Gonçalves-Alvim SJ, Korndorf G, Fernandes GW (2006) Sclerophylly in Qualea parviflora (Vochysiaceae): influence of herbivory, mineral nutrients, and water status. Plant Ecol 187:153–162
González-Zurdo P, Escudero A, Babiano J, García-Ciudad A, Mediavilla S (2016) Costs of leaf reinforcement in response to winter cold in evergreen species. Tree Physiol 36:273–286
Goulden ML (1996) Carbon assimilation and water-use efficiency by neighboring Mediterranean-climate oaks that differ in water access. Tree Physiol 16:417–424
González-Rebollar JL, García-Álvarez A, Ibáñez JJ (1995) A mathematical model for predicting the impact of climate changes on mediterranean plant landscapes. In: Zewer S, van Rompaey RSAR, Kok MTJ, Berk MM (eds) Climate change research: evaluation and policy implications. Elsevier, Amsterdam, pp 757–762
Grammatikopoulos G, Karabourniotis G, Kyparissis A, Petropoulou Y, Manetas Y (1994) Leaf hairs of olive (Olea europaea) prevent stomatal closure by ultraviolet-B radiation. Aust J Plant Physiol 21:293–301
Grassi G, Magnani F (2005) Stomatal, mesophyll conductance and biochemical limitations to photosynthesis as affected by drought and leaf ontogeny in ash and oak trees. Plant, Cell Environ 28:834–849
Griffin JR (1971) Oak regeneration in the upper Carmel Valley, California. Ecology 52:862–868
Griffin JR (1973) Xylem sap tension in three woodland oaks of central California. Ecology 54:152–159
Griffin JR (1977) Oak woodland. In: Barbour MG, Major J (eds) Terrestrial vegetation of California. Wiley, New York, pp 383–415
Groom P, Lamont BB (1997) Xerophytic implications of increased sclerophylly: interactions with water and light in Hakea psilorrhyncha seedlings. New Phytol 136:23–231
Groom PK, Lamont BB (1999) Which commn indices of sclerophylly best reflect differences in leaf structure? Ecoscience 6:471–474
Grove AT, Miles MR, Worthington EB, Doggett H, Dasgupta B, Farmer BH (1977) The geography of semi-arid lands [and discussion]. Philos Trans R Soc Lond B Biol Sci 278:457–475
Grubb PJ (1986) Sclerophylls, pachyphylls and pycnophylls: the nature and significance of hard leaf surfaces. In: Juniper B, Southwood R (eds) Insects and the plant surface. Edward Arnold, London, UK, pp 137–150
Hacke UG, Sperry JS, Wheeler JK, Castro L (2006) Scaling of angiosperm xylem structure with safety and efficiency. Tree Physiol 26:689–701
Hardin JW (1979) Patterns of variation in foliar trichomes of eastern North American Quercus. Am J Bot 66:576–585
He Y, Li N, Wang Z, Wang H, Yang G, **ao L, Wu J, Sun B (2014) Quercus yangyiensis sp. nov. from the late Pliocene of Baoshan, Yunnan and its paleoclimatic significance. Acta Geol Sin 88:738–747
Heide-Jorgensen HS (1990) Xeromorphic leaves of Hakea suaveolens R. Br. IV. Ontogeny, structure and function of the sclereids. Aust J Bot 38:25–43
Herrera CM (1992) Historical effects and sorting processes as explanations for contemporary ecological patterns: character syndromes in Mediterranean Woody plants. Am Nat 140:421–446
Himrane H, Camarero JJ, Gil-Pelegrín E (2004) Morphological and ecophysiological variation of the hybrid oak Quercus subpyrenaica (Q. faginea × Q. pubescens). Trees 18:566–575
Holloway PJ (1982) Structure and histochemistry of plant cuticular membranes: an overview. In: Cutler DF, Alvin KL, Price CE (eds) The plant cuticle. Academic Press, London, pp 1–32
Hurrell JW, Hoerling MP, Phillips AS, Xu T (2004) Twentieth century North Atlantic climate change. Part I: assessing determinism. Clim Dyn 23:371–389
Iovi K, Kolovou C, Kyparissis A (2009) An ecophysiological approach of hydraulic performance for nine Mediterranean species. Tree Physiol 29:889–900
Jacobsen AL, Pratt RB, Davis SD, Ewers FW (2007a) Cavitation resistance and seasonal hydraulics differ among three arid Californian plant communities. Plant Cell Envir 30:1599–1609
Jacobsen AL, Pratt RB, Ewers FW, Davis SD (2007b) Cavitation resistance among 26 chaparral species of Southern California. Ecol Monogr 77:99–115
Jacobsen AL, Esler KJ, Pratt RB, Ewers FW (2009) Water stress tolerance of shrubs in mediterranean type climate regions: convergence of fymbos and succulent karoo communities with California shrub communities. Am J Bot 96:1445–1453
Jacobsen AL, Pratt RB, Davis SD, Tobin MF (2014) Geographic and seasonal variation in chaparral vulnerability to cavitation. Madroño 61:317–327
Jeffree CE (1996) Structure and ontogeny of plant cuticles. In: Kerstiens G (ed) Plant cuticles: an integrated functional approach. Bios Scientific Publishers, Oxford, pp 33–82
Jiménez-Moreno G, Fauquette S, Suc JP (2010) Miocene to Pliocene vegetation reconstruction and climate estimates in the Iberian Peninsula from pollen data. Rev Palaeobot Palyno 162:403–415
Joffre R, Rambal S, Damesin C (2007) Functional attributes in Mediterranean-type ecosystems. In: Valladares F, Pugnaire FI (eds) Functional plant ecology, 2nd edn. CRC Press, Boca raton, Fl, USA, pp 285–312
John GP, Scoffoni C, Buckley TN, Villar R, Poorter H, Sack L (2017) The anatomical and compositional basis of leaf mass per area. Ecol Lett 20(4):412–425
Johnson HB (1975) Plant pubescence: an ecological perspective. Bot Rev 41:233–258
Johnson DM, Woodruff DR, McCullo KA, Meinzer FC (2009) Leaf hydraulic conductance, measured in situ, declines and recovers daily: leaf hydraulics, water potential and stomatal conductance in four temperate and three tropical tree species. Tree Physiol 29:879–887
Jordan GJ, Weston PH, Carpenter RJ, Dillon RA, Brodribb TJ (2008) The evolutionary relations of sunken, covered and encrypted stomata to dry habitats in Proteaceae. Am J Bot 95:521–530
Karabourniotis G, Bornman JF (1999) Penetration of UV-A, UV-B and blue light through the leaf trichome layers of two xeromorphic plants, olive and oak, measured by optical fibre microprobes. Physiol Plant 105:655–661
Kerstiens G (1996) Cuticular water permeability and its physiological significance. J Exp Bot 47:1813–1832
Kerstiens G (2006) Water transport in plant cuticles: an update. J Exp Bot 57:2493–2499
Kikuzawa K (1991) A cost-benefit analysis of leaf habit and leaf longevity of trees and their geographical pattern. Am Nat 138:1250–1263
Knox RG, Harcombe PA, Elsik IS (1995) Contrasting patterns of resource limitation in tree seedlings across a gradient in soil texture. Can J Forest Res 25:1583–1594
Kooyman RM, Laffan SW, Westoby M (2017) The incidence of low phosphorus soils in Australia. Plant Soil 412:143–150
Köppen W (1936) Das geographische system der klimate. In: Köppen W, Geiger R (eds) Handbuch der Klimatologie 3. Gebrueder Borntraeger, Berlin
Kouki M, Manetas Y (2002) Toughness is less important than chemical composition of Arbutus leaves in food selection by Poecilimon species. New Phytol 154:399–407
Kovar-Eder J (2003) Vegetation dynamics in Europe during the Neogene. In: Reumer JWF, Wessels W (eds) Distribution and migration of tertiary mamals in Eurasia. A volume in honour of Hans de Bruijn. Deinsea 10:373–392
Krichak SO, Alpert P (2005) Decadal trends in the East Atlantic/West Russiapattern and the Mediterranean precipitation. Int J Climatol 25:183–192
Kröber W, Zhang S, Ehmig M, Bruelheide H (2014) Linking xylem hydraulic conductivity and vulnerability to the leaf economics spectrum-A cross-species study of 39 evergreen and deciduous broadleaved subtropical tree species. PLoS ONE 9(11):e109211
Lamont BB, Groom PK, Cowling RM (2002) High leaf mass per area of related species assemblages may reflect low rainfall and carbon isotope discrimination rather than low phosphorus and nitrogen concentrations. Funct Ecol 16:403–412
Lasanta T, Nadal-Romero E, Errea P, Arnáez J (2016) The effect of landscape conservation measures in changing landscape patterns: a case study in mediterranean mountains. Land Degrad Dev 27(2):373–386
Leiva MJ, Fernández-Alés (1998) Variability in seedling water status during drought within a Quercus ilex subsp. ballota population, and its relation to seedling morphology. For Ecol Manag 111:147–156
Levin DA (1976) The chemical defenses of plants to pathogens and herbivores. Annu Rev Ecol Syst 7:121–159
Levitt J (1980) Responses of plants to environmental stresses. Volume 2, Water, radiation, salt and other stresses, 2nd edn. Academic Press, New York
Li Y, Sperry JS, Taneda H, Bush SE, Hacke UG (2008) Evaluation of centrifugal methods for measuring xylem cavitation in conifers, diffuse- and ring-porous angiosperms. New Phytol 177:558–568
Limousin JM, Misson L, Lavoir AV, Martin NK, Rambal S (2010a) Do photosynthetic limitations of evergreen Quercus ilex leaves change with long-term increased drought severity? Plant, Cell Environ 33:863–875
Limousin JM, Longepierre D, Huc R, Rambal S (2010b) Change in hydraulic traits of Mediterranean Quercus ilex subjected to long-term throughfall exclusion. Tree Physiol 30:1026–1036
Lionello, P, Malanotte-Rizzoli, P, Boscolo, R, et al (2006) The Mediterranean climate: an overview of the main characteristics and issues. In: Lionello P, Malanotte-Rizzoli P, R Boscolo R (eds). Mediterranean Climate Variability. Elsevier, Amsterdam, p 1–26
Lo Gullo MA, Salleo S, Rosso (1986) Drought avoidance strategy in Ceratonia Siliqua L., a mesomorphic-leaved tree in the Xeric Mediterranean area. Ann Bot 58:745–756
Lo Gullo MA, Salleo S (1988) Different strategies of drought resistance in three Mediterranean sclerophyllous trees growing in the same environmental conditions. New Phytol 108:267–276
Lo Gullo MA, Salleo S (1993) Different vulnerabilities of Quercus ilex L. to freezeand summer drought-induced xylem embolism: an ecological interpretation. Plant, Cell Environ 16:511–519
Lo Gullo M, Nardini A, Trifilò P, Salleo S (2005) Diurnal and seasonal variations in leaf hydraulic conductance in evergreen and deciduous trees. Tree Physiol 25:505–512
Loveless AR (1961) A nutrítional interpretation of sclerophylly based on differences in the chemical composition of sclerophyllous and mesophytic leaves. Ann Bot 25:168–184
Loveless AR (1962) Further evidence to support a nutritional interpretation of sclerophylly. Ann Bot 26:551–561
Lucas PW, Pereira B (1990) Estimation of the fracture toughness of leaves. Funct Ecol 4:819–822
Lumaret R, Mir C, Michaud H, Raynal V (2002) Phylogeographical variation of chloroplast DNA in holm oak (Quercus ilex L.). Mol Ecol 11:2327–2336
Maherali H, Pockman WT Jackson RB (2004) Adaptive variation in the vulnerability of woody plants to xylem cavitation. Ecology 85:2184–2199
Maherali H, Moura CF, Caldeira MC, Willson CJ, Jackson RB (2006) Functional coordination between leaf gas exchange and vulnerability to xylem cavitation in temperate forest trees. Plant, Cell Environ 29:571–583
Mai DH (1991) Palaeofloristic changes in Europe and the confirmation of the arctotertiary-palaeotropical geoflora concept. Rev Palaeobot Palyno 68:29–36
Maire V, Wright IJ, Prentice IC, Batjes NH, Bhaskar R, van Bodegom PM, Cornwell WK, Ellsworth D, Niinemets U, Ordonez A, Reich PB, Santiago LS (2015) Global effects of soil and climate on leaf photosynthetic traits and rates. Global Ecol Biogeogr 24:706–717
Manes F, Vitale M, Donato E, Giannini M, Puppi G (2006) Different ability of three Mediterranean oak species to tolerate progressive water stress. Photosynthetica 44(3):387–393
Manetas Y (2003) The importance of being hairy: the adverse effects of hair removal on stem photosynthesis of Verbascum speciosum are due to solar UV-B radiation. New Phytol 158:503–508
Mantua NJ, Hare SR, Zhang Y, Wallace JM, Francis RC (1997) A pacific interdecadal climate oscillation with impacts on salmon production. B Am Meteorol Soc 78:1069–1079
Mariotti A, Zeng N, Lau KM (2002) Euro-Mediterranean rainfall and ENSO a seasonally varying relationship. Geophys Res Lett 29:1621
Martínez-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
Martínez-Vilalta J, Cochard H, Mencuccini M, Sterck F, Herrero A, Korhonen JFJ, Llorens P, Nikinmaa E, Nolè A, Poyatos R, Ripullone F, Sass-Klaassen U, Zweifel R (2009) Hydraulic adjustment of Scots pine across Europe. New Phytol 184:353–364
McDonald PG, Fonseca CR, Overton JM, Westoby M (2003) Leaf-size divergence along rainfall and soil-nutrient gradients: is the method of size reduction common among clades? Funct Ecol 17:50–57
Mediavilla S, Escudero A (2003) Stomatal responses to drought at a Mediterranean site: a comparative study of co-occurring woody species differing in leaf longevity. Tree Physiol 23:987–996
Mediavilla S, Escudero A (2004) Stomatal responses to drought of mature trees and seedlings of two co-occurring Mediterranean oaks. For Ecol Manag 187:281–294
Mediavilla S, García-Ciudad A, García-Criado B, Escudero A (2008) Testing the correlations between leaf life span and leaf structural reinforcement in 13 species of European Mediterranean woody plants. Funct Ecol 22:787–793
Medrano H, Flexas J, Galmés (2008) Variability in water use efficiency at the leaf level among Mediterranean plants with different growth forms. Plant Soil 317:17–29
Meher-Homji (1973) A phytoclimatic approach to the problem of Mediterraneity in the Indo-Pakistan sub-continent. Feddes-Repertorium 83:757–788
Michaud H, Toumi HL, Lumaret R, Li TX, Romane F, Di Giusto F (1995) Effect of geographical discontinuity on genetic variation in Quercus ilex L. (holm oak). Evidence from enzyme polymorphism. Heredity 74:590–606
Millar CI (2012) Geologic, climatic, and vegetation history of California. In: Baldwin BG, Goldman DH, Keil DJ, Patterson R, Rosatti TJ, Wilken DH (eds) The Jepson Manual: Vascular Plants of California, 2nd edn. University of California Press, pp 49–67
Mitrakos KA (1980) A theory for Mediterranean plant life. Acta Oecol 1:245–252
Mitrakos K (1982) Winter low temperatures in mediterranean-type ecosystems. Ecol Mediterr 8:95–102
Montserrat-Martí G, Camarero JJ, Palacio S, Pérez-Rontomé C, Milla R, Albuixech J, Maestro M (2009) Summer-drought constrains the phenology and growth of two co-existing Mediterranean oaks with contrasting leaf habit: implications for their persistence and reproduction. Trees 23:787–799
Mooney HA, Dunn EL (1970) Convergent evolution of Mediterranean-climate evergreen sclerophyll shrubs. Evolution 24:292–303
Mooney HA (1982) Habitat, plant form, and plant water relations in Mediterranean-climate regions. Ecol Mediterr 8:287–296
Morales F, Abadía A, Abadía J Montserrat G, Gil-Pelegrín E (2002) Trichomes and photosynthetic pigment composition changes: responses of Quercus ilex subsp. ballota (Desf.) Samp. and Quercus coccifera L. to Mediterranean stress conditions. Trees 16:504–510
Morecroft MD, Roberts JM (1999) Photosynthesis and stomatal conductance of mature canopy Oak (Quercus robur) and Sycamore (Acer pseudoplatanus) trees throughout the growing season. Funct Ecol 13:332–342
Moreno G, Gallardo JF, Vicente MA (2011) How mediterranean deciduous trees cope with long summer drought? The case of Quercus pyrenaica forests in western Spain. In: Bredemeier M, Cohen S, Godbold DL, Lode E, Pichler V, Schleppi P (eds) Forest management and the water cycle. An ecosystem-based approach. Ecological Studies 212, Springer, Dordrecht, pp 181–207
Nardini A, Lo Gullo MA, Tracanelli S (1996) Water relations of six sclerophylls growing near Trieste (Northeastern ltaly): has sclerophylly a univocal functional significance? Giorn Bot Ital 130:811–828
Nardini A, Lo Gullo MA, Salleo S (1999) Competitive strategies for water availability in two Mediterranean Quercus species. Plant, Cell Environ 22:109–116
Nardini A, Pedà G, La Rocca N (2012a) Trade-offs between leaf hydraulic capacity and drought vulnerability: morpho-anatomical bases, carbon costs and ecological consequences. New Phytol 196:788–798
Nardini A, Pedá G, Salleo S (2012b) Alternative methods for scaling leaf hydraulic conductance offer new insights into the structure–function relationships of sun and shade leaves. Funct Plant Biol 39:394–401
Nardini A, Lo Gullo MA, Truifilo P, Salleo S (2014) The challenge of the Mediterranean climate to plant hydraulics: responses and adaptations. Environ Exp Bot 103:68–79
Negi SS, Naithani HB (1995) Oaks of India, Nepal and Bhutan. International Book Distributors, Dehra Dun, India
Nixon KC (2002) The oak (Quercus) biodiversity of California and adjacent regions. USDA Forest Service Gen Tech Rep. PSW-GTR-184
Nicotra AB, Cosgrove MJ, Cowling A, Schlichting CD, Jones CS (2008) Leaf shape linked to photosynthetic rates and temperature optima in South African Pelargonium species. Oecologia 154:625–635
Niinemets U (2001) Global-scale climatic controls of leaf dry mass per area, density, and thickness in trees and shrubs. Ecology 82:453–469
Niinemets Ü, Cescatti A, Rodeghiero M, Tosens T (2005) Leaf internal conductance limits photosynthesis more strongly in older leaves of Mediterranean evergreen broad-leaved species. Plant, Cell Environ 28:1552–1556
Niinemets Ü, Keenan T (2014) Photosynthetic responses to stress in Mediterranean evergreens: mechanisms and models. Environ Exp Bot 103:24–41
Niinemets Ü (2015) Is there a species spectrum within the world-wide leaf economics spectrum? Major variations in leaf functional traits in the Mediterranean sclerophyll Quercus ilex. New Phytol 205:79–96
Niinemets Ü (2016) Does the touch of cold make evergreen leaves tougher? Tree Physiol 36:267–272
Niklas KJ (1999) A mechanical perspective on foliage leaf form and function. New Phytol 143:19–31
Nobel (1991) Physicochemical and environmental plant physiology. Academic Press, San Diego
Noce S, Collalti A, Valentini R, Santini M (2016) Hot spot maps of forest presence in the Mediterranean Basin. iForest 9:766
Oertli JJ (1986) The effect of cell size on cell collapse under negative turgor pressure. J Plant Physiol 124:365–370
Oertli JJ, Lips SH, Agami M (1990) The strength of sclerophyllous cells to resist collapse due to negative turgor pressure. Acta Oecol 11:281–289
Ogaya R, Peñuelas J (2003) Phenological patterns of Quercus ilex, Phillyrea latifolia, and Arbutus unedo growing under a field experimental drought. Écoscience 11:263–270
Ogaya R, Peñuelas J (2007) Leaf mass per area ratio in Quercus ilex leaves under a wide range of climatic conditions. The importance of low temperatures. Acta Oecol 31:168–173
Oliveira G, Peñuelas J (2002) Comparative protective strategies of Cistus albidus and Quercus ilex facing photoinhibitory winter conditions. Environ Exp Bot 47:281–289
Onoda Y, Westoby M, Adler PB, Choong AMF, Clissold FJ, Cornelissen JHC, Díaz S, Dominy NJ, Elgart A, Enrico L, Fine PVA, Howard JJ, Jalili A, Kitajima K, Kurokawa H, McArthur C, Lucas PW, Markesteijn L, Perez- Harguindeguy N, Poorter L, Richards L, Santiago LS, Sosinski EE, van Bael SA, Warton DI, Wright IJ, Wright SJ, Yamashita N (2011) Global patterns of leaf mechanical properties. Ecol Lett 14:301–312
Paddock WA III, Davis SD, Pratt RB, Jacobsen AL, Tobin MF, López-Portillo J, Ewers FW (2013) Factors determining mortality of adult chaparral shrubs in an extreme drought year in California. Aliso 31:49–57
Panahi P, Jamzad Z, Pourmajidian MR, Fallah A, Pourhashemi M (2012a) Foliar epidermis morphology in Quercus (subgenus Quercus, section Quercus) in Iran. Acta Bot Croat 71:95–113
Panahi P, Jamzad Z, Pourmajidian MR, Fallah A, Pourhashemi M, Sohrabi H (2012b) Taxonomic revision of the Quercus brantii complex (Fagaceae) in Iran with emphasis on leaf and pollen micromorphology. Acta Bot Hung 54(3–4):355–375
Pasho E, Camarero JJ, de Luis M, Vicente-Serrano SM (2011) Impacts of drought at different time scales on forest growth across a wide climatic gradient in north-eastern Spain. Agr Forest Meteorol 151:1800–1811
Peel MC, Finlayson BL, McMahon TA (2007) Updated world map of the Köppen-Geiger climate classification. Hydrol Earth Syst Sci Discuss 4:439–473
Peeters PJ, Sanson G, Read J (2007) Leaf biomechanical properties and the densities of herbivorous insect guilds. Funct Ecol 21:246–255
Peguero-Pina JJ, Sancho-Knapik D, Cochard H, Barredo G, Villarroya D, Gil-Pelegrín E (2011) Hydraulic traits are associated with the distribution range of two closely related Mediterranean firs, Abies alba M. and Abies pinsapo Boiss. Tree Physiol 31:1067–1075
Peguero-Pina JJ, Sancho-Knapik D, Barrón E, Camarero JJ, Vilagrosa A, Gil-Pelegrín E (2014) Morphological and physiological divergences within Quercus ilex support the existence of different ecotypes depending on climatic dryness. Ann Bot 114:301–313
Peguero-Pina JJ, Sancho-Knapik D, Martín P, Saz MA, Gea-Izquierdo G, Cañellas I, Gil-Pelegrín E (2015) Evidence of vulnerability segmentation in a deciduous Mediterranean oak (Quercus subpyrenaica E. H. del Villar). Trees 29:1917–1927
Peguero-Pina JJ, Sisó S, Sancho-Knapik D, Díaz-Espejo Flexas J, Galmés J, Gil-Pelegrín E (2016a) Leaf morphological and physiological adaptations of a deciduous oak (Quercus faginea Lam.) to the Mediterranean climate: a comparison with a closely related temperate species (Quercus robur L.). Tree Physiol 36:287–299
Peguero-Pina JJ, Sisó S, Fernández-Marín B, Flexas J, Galmés J, García-Plazaola JI, Niinemets Ü, Sancho-Knapik D, Gil-Pelegrín E (2016b) Leaf functional plasticity decreases the water consumption without further consequences for carbon uptake in Quercus coccifera L. under Mediterranean conditions. Tree Physiol 36:356–367
Peguero-Pina JJ, Sisó S, Flexas J, Galmés J, García-Nogales A, Niinemets Ü, Sancho-Knapik D, Saz MA, Gil-Pelegrín E (2017a) Cell-level anatomical characteristics explain high mesophyll conductance and photosynthetic capacity in sclerophyllous Mediterranean oaks. New Phytol 214:585–596
Peguero-Pina JJ, Sancho-Knapik D, Gil-Pelegrín E (2017b) Ancient cell structural traits and photosynthesis in today’s Environment. J Exp Bot 68:1389–1392
Peñuelas J, Filella I, Llusià J, Siscart D, Piñol J (1998) Comparative field study of spring and summer leaf gas exchange and photobiology of the mediterranean trees Quercus ilex and Phillyrea latifolia. J Exp Bot 49:229–238
Pérez-Estrada LB, Cano-Santana Z, Oyama K (2000) Variation in leaf trichomes of Wigandia urens: environmental factors and physiological consequences. Tree Physiol 20:629–632
Pesoli P, Gratani L, Larcher W (2003) Responses of Quercus ilex from different provenances to experimentally imposed water stress. Biol Plantarum 46:577–581
Pinto CA, David JS, Cochard H, Caldeira MC, Henriques MO, Quilhó T, Paço TA, Pereira JS, David TS (2012) Drought-induced embolism in current-year shoots of two Mediterranean evergreen oaks. Forest Ecol Manag 285:1–10
Pratt RB, Jacobsen AL, Golgotiu KA, Sperry JS, Ewers FW Davis SD (2007) Life history type and water stress tolerance in nine California chaparral species (Rhamnaceae). Ecol Monogr 77:239–253
Poudyal K, Jha PK, Zobel DB, Thapa CB (2004) Patterns of leaf conductance and water potentila of five Himalayan tree species. Tree Physiol 24:689–699
Poyatos R, Llorens P, Piñol J, Rubio C (2008) Response of Scots pine (Pinus sylvestris L.) and pubescent oak (Quercus pubescensWilld.) to soil and atmospheric water deficits under Mediterranean mountain climate. Ann For Sci 65:306
Pozo-Vázquez D, Esteban-Parra MJ, Rodrigo FS, Castro-Diez Y (2001) A study of NAO variability and its possible non-linear influences on European Surface temperature. Clim Dyn 17:701–715
Radoglou K (1996) Environmental control of CO2 assimilation rates and stomatal conductance in five oak species growing under field conditions in Greece. Ann Sci Forest 53:269–278
Read J, Sanson GD (2003) Characterising sclerophylly: the mechanical properties of a diverse range of leaf types. New Phytol 160:81–99
Read J, Sanson GD, Lamont BB (2005) Leaf mechanical properties in sclerophyll woodland and shrubland on contrasting soils. Plant Soil 276:95–113
Read J, Sanson G, De Garine-Wichatitsky M, Tanguy J (2006) Sclerophylly in two contrasting tropical environments: low nutrients versus low rainfall. Am J Bot 93:1601–1614
Read J, Sanson GD, Caldwell E, Clissold F, Chatain A, Peeters P, Lamont BB, De Garine-Wichatitsky M, Jaffré T, Stuart Kerr S (2009) Correlations between leaf toughness and phenolics among species in contrasting environments of Australia and New Caledonia. Ann Bot 103:757–767
Read J, Sanson G, Trautmann MF (2016) Leaf traits in Chilean matorral: Sclerophylly within, among, and beyond matorral, and its environmental determinants. Ecol Evol 6:1430–1446
Reale O, Dirmeyer P (2000) Modeling the effects of vegetation on Mediterranean climate during the Roman classical period—Part I: climate history and model sensitivity. Global Planet 25:163–184
Reille M, Pons A (1992) The ecological significance of sclerophyllous oak forests in the western part of the Mediterranean Basin: a note on pollen analytical data. Vegetatio 99–100:13–17
Retallack GJ (2004) Late Miocene climate and life on land in Oregon within a context of Neogene global change. Palaeogeogr Palaeocl 214:97–123
Ribeiro SP, Basset Y (2007) Gall-forming and free-feeding herbivory along vertical gradients in a lowland tropical rainforest: the importance of leaf sclerophylly. Ecography 30:663–672
Riera-Mora S, Esteban-Amat A (1994) Vegetation history and human activity during the last 6000 years on the central Catalan coast (north-eastern Iberian Peninsula). Veg His Archaebot 3:7–23
Rico M, Gallego HA, Moreno G, Santa Regina I (1996) Stomatal response of Quercus pyrenaica Willd to environmental factors in two sites differing in their annual rainfall (Sierra de Gata, Spain). Ann Sci For 53:221–234
Riederer M, Schreiber L (2001) Protecting against water loss: analysis of the barrier properties of plant cuticles. J Exp Bot 52:2023–2032
Ripley BS, Pammenter NW, Smith VR (1999) Function of leaf hairs revisited: the hair layer on leaves of Arctotheca populifolia reduces photoinhibition, but leads to higher leaf temperatures caused by lower transpiration rates. J Plant Physiol 155:78–85
Rivas-Martínez S, Rivas-Sáenz S, Penas-Merino A (2011) Worldwide bioclimatic classification system. Global geobotany 1:1–634
Roth-Nebelsick A, Hassiotou F, Veneklaas EJ (2009) Stomatal crypts have small effects on transpiration: a numerical model analysis. Plant Physiol 151:2018–2027
Roth-Nebelsick A, Fernández V, Peguero-Pina JJ, Sancho-Knapik D, Gil-Pelegrín E (2013) Stomatal encryption by epicuticular waxes as a plastic trait modifying gas exchange in a Mediterranean evergreen species (Quercus coccifera L.). Plant, Cell Environ 36:579–589
Rubio de Casas R, Vargas P, Pérez-Corona E, Cano E, Manrique E, García-Verdugo C, Balaguer L (2009) Variation in sclerophylly among Iberian populations of Quercus coccifera L. is associated with genetic differentiation across contrasting environments. Plant Biology 11:464–472
Rundel PW, Arroyo MTK, Cowling RM, Keeley JE, Lamont BB, Vargas P (2016) Mediterranean biomes: evolution of their vegetation, floras, and climate. Ann Rev Ecol Evol S 47:383–407
Sack L, Scoffoni C, McKown AD, Frole K, Rawls M, Havran JC, Tran H, Tran T (2012) Developmentally based scaling of leaf venation architecture explains global ecological patterns. Nat Commun 3:837
Salleo S, Gullo Lo (1990) Sclerophylly and plant water relations in three Mediterranean Quercus species. Ann Bot 65:259–270
Salleo S, Nardini A, Lo Gullo MA (1997) Is sclerophylly of Mediterranean evergreens an adaptation to drought? New Phytol 135:603–612
Salleo S, Nardini A (2000) Sclerophylly: evolutionary advantage or mere epiphenomenon? Plant Biosyst 134:247–259
Salleo S, Pitt F, Nardini A, Hamzé M, Jomaa I (2002) Differential drought resistance of two Mediterranean oaks growing in the Bekaa Valley (Lebanon). Plant Biosyst 136:91–99
Sánchez de Dios R, Benito-Garzón M, Sainz-Ollero H (2009) Present and future extension of the Iberian submediterranean territories as determined from the distribution of marcescent oaks. Plant Ecol 204:189–205
Sancho-Knapik D, Alvarez-Arenas TG, Peguero-Pina JJ, Fernández V, Gil-Pelegrín E (2011) Relationship between ultrasonic properties and structural changes in the mesophyll during leaf dehydration. J Exp Bot 62:3637–3645
Sardans J, Rodá F, Peñuelas J (2004) Phosphorus limitation and competitive capacities of Pinus halepensis and Quercus ilex subsp. rotundifolia on different soils. Plant Ecol 174:305–317
Sardans J, Peñuelas J (2013) Plant-soil interactions in Mediterranean forest and shrublands: impacts of climatic change. Plant Soil 365:1–33
Savé R, Castell C, Terradas J (1999) Gas exchange and water relations. In: Roda F, Retana J, Gracia CA, Bellot J (eds) Ecology of Mediterranean Evergreen Oak forests. Ecological studies 137. Springer, Berlin, pp 135–146
Savé R, Biel C, de Herralde F (2000) Leaf pubescence, water relations and chlorophyll fluorescence in two subspecies of Lotus creticus L. Biol Plant 43:239–244
Scarascia-Mugnozza G, Oswald H, Piussi P, Radoglou K (2000) Forests of the Mediterranean region: gaps in knowledge and research needs. Forest Ecol Manag 132:97–109
Scareli-Santos C, Sánchez-Mondragón ML, González-Rodríguez A, Oyama K (2013) Foliar micromorphology of Mexican oaks (Quercus: Fagaceae). Acta Bot Mex 104:31–52
Schimper AFW (1903) Plant-geography on a physiological basis. Clarendon Press, Oxford
Schreuder MDJ, Brewer CA, Heine C (2001) Modelled influences of non-exchanging trichomes on leaf boundary layers and gas exchange. J Theor Biol 210:23–32
Scoffoni C, Rawls M, McKown A, Cochard H, Sack L (2011) Decline of leaf hydraulic conductance with dehydration: relationship to leaf size and venation architecture. Plant Physiol 156:832–843
Seddon G (1974) Xerophytes, xeromorphs and sclerophylls: the history of some concepts in ecology. Biol J Linn Soc 6:65–87
Serrano L, Peñuelas J, Ogaya R, Savé R (2005) Tissue-water relations of two co-occurring evergreen Mediterranean species in response to seasonal and experimental drought conditions. J Plant Res 118:263–269
Serrano-Muela MP, Nadal-Romero E, Lana-Renault N, González-Hidalgo JC, López-Moreno JI, Beguería S, Sanjuan Y, García-Ruiz JM (2013) An exceptional rainfall event in the central western Pyrenees: spatial patterns in discharge and impact. Land Degrad Dev 26(3):249–262
Shmida A (1981) Mediterranean vegetation in California and Israel: similarities and differences. Israel J Bot 30:105–123
Shmida A, Whittaker RH (1984) Convergence and non-convergence of Mediterranean type communities in the old and the new world. In: Margaris NS, Arianoustou-Farragitaki M, Oechel WC (eds) Being alive on land. Dr W. Junk, The Hague, pp 5–11
Siam AMJ, Radoglou KM, Noitsakis B, Smiris P (2009) Differences in ecophysiological responses to summer drought between seedlings of three deciduous oak species. Forest Ecol Manag 258:35–42
Singh SP, Zobel DB, Garkoti SC, Tewari A, Negi CMS (2006) Patterns in water relations of central Himalayan trees. Trop Ecol 47:159–182
Sisó S, Camarero JJ, Gil-Pelegrín E (2001) Relationship between hydraulic resistance and leaf morphology in broadleaf Quercus species: a new interpretation of leaf lobation. Trees 15:341–345
Sperry JS, Tyree MT (1988) Mechanism of water-stress induced embolism. Plant Physiol 88:581–587
Sperry JS, Christman MA, Torres-Ruiz JM, Taneda H, Smith DD (2012) Vulnerability curves by centrifugation: is there an open vessel artefact, and are ‘r’ shaped curves necessarily invalid? Plant, Cell Environ 35:601–610
Sobrado MA, Medina E (1980) General Morphology, anatomical structure, and nutrient content of sclerophyllous leaves of the ‘Bana’ vegetation of amazonas. Oecologia 45:341–345
Suc JP (1984) Origin and evolution of the Mediterranean vegetation and climate in Europe. Nature 307:429–432
Sultan SE, Bazzaz FA (1993) Phenotypic plasticity in Polygonum persicaria. II. Norms of reaction to soil-moisture and the maintenance of genetic diversity. Evolution 47:1032–1049
Thompson JD (2005) Plant Evolution in the Mediterranean. Oxford University Press, Oxford
Tobin MF, Pratt RB, Jacobsen AL, De Guzman ME (2013) Xylem vulnerability to cavitation can be accurately characterised in species with long vessels using a centrifuge method. Plant Biol 15:496–504
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 139:347–448
Tognetti R, Longobucco A, Raschi A (1999) Seasonal embolism and xylem vulnerability in deciduous and evergreen Mediterranean trees influenced by proximity to a carbon dioxide spring. Tree Physiol 19:271–277
Tognetti R, Cherubini P, Marchi S, Raschi A (2007) Leaf traits and tree rings suggest different water-use and carbon assimilation strategies by two co-occurring Quercus species in a Mediterranean mixed-forest stand in Tuscany, Italy. Tree Physiol 27:1741–1751
Traiser C, Klotz S, Uhl D, Mosbrugger V (2005) Environmental signals from leaves—a physiognomic analysis of European vegetation. New Phytol 166:465–484
Trigo RM, García-Herrera R, Díaz J, Trigo IF, Valente A (2005) How exceptional was the early August 2003 heatwave in France. Geophys Res Lett 32:L10701
Trouet V, Taylor AH, Carleton AM et al (2009) Interannual variations in fire weather, fire extent, and synoptic-scale circulation patterns in northern California and Oregon. Theor Appl Climatol 95:349
Turner IM (1994) Sclerophylly: primarily protective? Funct Ecol 8:669–675
Tyree MT, Cochard H (1996) Summer and winter embolism in oak. Impact on water relations. Ann Sci Forest 53:173–180
Urbieta IR, Zavala MA, Marañón T (2008) Human and non-human determinants of forest composition in Southern Spain: evidence of shifts towards cork oak dominance as a result of management over the ast century. J Biogeogr 35:1688–1700
Urli M, Porté AJ, Cochard H, Guengant Y, Burlett R, Delzon S (2013) Xylem embolism threshold for catastrophic hydraulic failure in angiosperm trees. Tree Physiol 33:672–683
Valero-Galván J, González-Fernández R, Navarro-Cerrillo R, Gil-Pelegrín E, Jorrín-Novo JV (2013) Physiological and proteomic analyses of drought stress response in holm oak rovenances. J Proteome Res 12:5110–5123
Valero-Galván J, Valledor L, Navarro-Cerrillo R, Gil-Pelegrín E, Jorrín-Novo JV (2011) Studies of variability in Holm oak (Quercus ilex subsp. ballota [Desf.] Samp.) through acorn protein profile analysis. J Proteomics 74:1244–1255
Valiente-Banuet A, Rumebe AV, Verdú M, Callaway RM (2006) Modern quaternary plant lineages promote diversity through facilitation of ancient tertiary lineages. PNAS 103:16812–16817
Vankat JL (1982) A gradient perspective on the vegetation of Sequoia National Park, California. Madrorño 29:200–214
Vaz M, Pereira JS, Gazarini LC, David TS, David JS, Rodrigues A, Maroco J, Chaves MM (2010) Drought-induced photosynthetic inhibition and autumn recovery in two Mediterranean oak species (Quercus ilex and Quercus suber). Tree Physiol 30:946–956
Vaz M, Cochard H, Gazarini L, Graça J, Chaves MM, Pereira JS (2012) Cork oak (Quercus suber L.) seedlings acclimate to elevated CO2: photosynthesis, growth, wood anatomy and hydraulic conductivity. Trees 26:1145–1157
Venturas MD, Rodriguez-Zaccaro FD, Percolla MI, Crous CJ, Jacobsen AL, Pratt RB (2016a) Single vessel air injection estimates of xylem resistance to cavitation are affected by vessel network characteristics and sample length. Tree Physiol 36:1247–1259
Venturas MD, MacKinnon ED, Dario HL, Jacobsen AL, Pratt RB, Davis SD (2016b) Chaparral shrub hydraulic traits, size, and life history types relate to species mortality during California’s historic drought of 2014. PLoS ONE 11(7):e0159145
Verdú M, Dávila P, García-Fayos P, Flores-Hernández N, Valiente-Banuet A (2003) ‘Convergent’ traits of Mediterranean woody plants belong to pre-Mediterranean lineages. Biol J Linn Soc 78:415–427
Verdú M, Pausas JG, Segarra-Moragues JG, Ojeda F (2007) Burning phylogenies: fire, molecular evolutionary rates, and diversification. Evolution 61:2195–2204
Verheye W, de la Rosa D (2005) Mediterranean soils. In: Land use and land cover from encyclopedia of life support systems (EOLSS), Developed under the Auspices of the UNESCO, Eolss Publishers, Oxford, UK
Vertovec M, Sakçali S, Ozturk M, Salleo S, Giacomich P, Feoli E, Nardini A (2001) Diagnosing plant water status as a tool for quantifying water stress, on a regional basis in Mediterranean drylands. Ann For Sci 58:113–125
Vilagrosa A, Cortina J, Gil-Pelegrín E, Bellot J (2003a) Suitability of drought-preconditioning techniques in Mediterranean climate. Restor Ecol 11:208–216
Vilagrosa A, Bellot J, Vallejo VR, Gil-Pelegrín E (2003b) Cavitation, stomatal conductance, and leaf dieback in seedlings of two co-occurring Mediterranean shrubs during an intense drought. J Exp Bot 54:2015–2024
Vilagrosa A, Morales F, Abadía A, Bellot J, Cochard H, Gil-Pelegrin E (2010) Are symplast tolerance to intense drought conditions and xylem vulnerability to cavitation coordinated? An integrated analysis of photosynthetic, hydraulic and leaf level processes in two Mediterranean drought-resistant species. Environ Exp Bot 69:233–242
Vilagrosa A, Chirino E, Peguero-Pina JJ, Barigah TS, Cochard H, Gil-Pelegrín E (2012) Xylem cavitation and embolism in plants living in water-limited ecosystems. In: Aroca R (ed) Plant responses to drought stress. Springer, Berlin, pp 63–109
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
Villar-Salvador P, Planelles R, Oliet J, Peñuelas-Rubira JL, Jacobs DF, González M (2004) Drought tolerance and transplanting performance of holm oak (Quercus ilex) seedlings after drought hardening in the nursery. Tree Physiol 4:1147–1155
Vogel S (2009) Leaves in the lowest and highest winds: temperature, force and shape. New Phytol 183:13–26
Wagner GJ, Wang E, Shepherd RW (2004) New approaches for studying and exploiting an old protuberance, the plant trichome. Ann Bot 93:3–11
Wallace JM, Gutzler DS (1981) Teleconnections in the geopotential height field during the Northern Hemisphere winter. Mon Weather Rev 109:784–812
Wallen CC (1970) Climates of Central and Southern Europe. World survey of climatology Volume 6. Elsevier Scientific Publishing Co, Amsterdam
Walter H (1985) Vegetation of the Earth and ecological systems of the geo-biosphere, 3rd edn. Springer, Berlin, p 318
Westbrook JW, Kitajima K, Burleigh JG, Kress WJ, Erickson DL, Wright SJ (2011) What makes a leaf tough? Patterns of correlated evolution between leaf toughness traits and demographic rates among 197 shade-tolerant woody species in a neotropical forest. Am Nat 177:800–811
Withington JM, Reich PB, Oleksyn j, Eissenstat DM (2006) Comparisons of structure and life Span in roots and leaves among temperate trees. Ecol Monogr 76:381–397
Witkowski ETF, Lamont BB (1991) Leaf specific mass confounds leaf density and thickness. Oecologia 88:486–493
Wright W, Vincent JFV (1996) Herbivory and the mechanics of fracture in plants. Biol Rev Camb Philos Soc 71:401–413
Xu L, Baldocchi DD (2003) Seasonal trends in photosynthetic parameters and stomatal conductance of blue oak (Quercus douglasii) under prolonged summer drought and high temperature. Tree Physiol 23:865–877
Yates MJ, Verboom GA, Rebelo AG, Cramer MD (2010) Ecophysiological significance of leaf size variation in Proteaceae from the Cape Floristic Region. Funct Ecol 24:485–492
Zhang SB, Zhou ZK, Hu H, Xu K, Yan N, Li SY (2005) Photosynthetic performances of Quercus pannosa vary with altitude in the Hengduan Mountains, Southwest China. Forest Ecol Manag 212:291–30
Zhang YJ, Rockwell FE, Graham AC, Alexander T, Holbrook NM (2016) Reversible leaf xylem collapse: a potential “circuit breaker” against cavitation. Plant Physiol 172:2261–2274
Zhu F, Yoh M, Gilliam FS, Lu X, Mo J (2013) Nutrient limitation in three lowland tropical forests in southern China receiving high nitrogen deposition: insights from fine root responses to nutrient additions. PLoS ONE 8(12):e82661
Acknowledgements
We thank Elena Martí Beltrán for her valuable help in the search of the species distribution. We thank also Francisco Garin García for his meaningful support in the recollection of oak leaves and identification of the species. We thank Jardín Botánico de Iturrarán for allowing us the recollection of the oak species used in the analysis on this chapter. Work of D S-K is supported by a DOC INIA contract co-funded by INIA and ESF.
Author information
Authors and Affiliations
Corresponding author
Editor information
Editors and Affiliations
Appendices
Appendix 5.1
List of Quercus species (scientific name, infrageneric group according to Denk and Grimm (2009) and distribution) used in the figures of the chapter. Species are classified into six groups according to: (i) their leaf habit (evergreen or winter deciduous ) and (ii) their climatic distribution conditions (Temperate , Tropical , Mediterranean or Arid ). For this purpose, geographical distribution coordinates for each species were obtained from herbarian data (Appendix 5.2) and overlapped on the climatic Köppen map. Köppen categories and zonobiomes sensu Walter (in brackets) are classified in four main groups: (i) temperate , without dry season (green); (ii) tropical , dry winter (blue); (iii) mediterranean, dry summer (red); and (iv) arid , arid (orange). For each group, represented by a particular colour, Köppen categories are listed according to their respective relevance.
Appendix 5.2
List of data sources for species distribution.
-
Archbold Biological Station (www.archbold-station.org)
-
California State Parks (https://www.parks.ca.gov)
-
CNPS Inventory Database (www.rareplants.cnps.org/simple.html)
-
Delta State University (www.deltastate.edu)- Harvard University Herbaria (https://huh.harvard.edu/pages/digital-resources,kiki.huh.harvard.edu/databases)
-
Desert Botanical Garden Herbarium Collection (https://www.dbg.org/desert-plant-research-center)
-
Eastern Michigan University Herbarium (www.emich.edu/biology/facilities/herbarium.php)
-
Fairchild Tropical Botanic Garden Virtual Herbarium (www.virtualherbarium.org)
-
Global Biodiversity Information Facility (GBIF) (http://www.gbif.org)
-
Herbarium WU Institute of Botany, University of Vienna (http://herbarium.univie.ac.at)
-
Illinois Natural History Survey (www.inhs.illinois.edu)
-
Intermountain Herbarium Utah State University (http://intermountainbiota.org)
-
Instituto Nacional de Tecnología Agraria y Alimentaria. INIA (http://wwwx.inia.es/herbario/herbarioweb/default.asp?tabla=quercus)
-
Kathryn Kalmbach Herbarium (www.gbif.org/dataset)
-
Mountains Restoration Trust (www.mountainstrust.org-New York Botanical Garden (https://www.nybg.org)
-
New York Botanical Garden Vascular Plant Database (http://sciweb.nybg.org/science2/hcol/allvasc/index.asp)
-
Royal Botanical Garden Edinburgh (www.rbge.org.uk)
-
Southwest Environmental Information Network-SEINet Arizona-New Mexico Chapter (http://swbiodiversity.org/seinet/collections)
-
The Jepson Herbarium , University of California Berkeley (http://ucjeps.berkeley.edu/interchange)
-
Plant Atlas. USF Water Institute, University of South Florida (http://www.plantatlas.usf.edu/)
-
Tall Timbers Research Station University of Southern Mississippi Herbarium (http://www.herbarium.bio.fsu.edu)—UCLA Herbarium (https://sites.lifesci.ucla.edu/eeb-herbarium /)—University of Arizona Herbarium (https://cals.arizona.edu/herbarium/content/specimens)
-
University of British Columbia Herbarium (www.biodiversity.ubc.ca/museum/herbarium)
-
University of Florida Herbarium (https://www.floridamuseum.ufl.edu/herbarium)
Rights and permissions
Copyright information
© 2017 Springer International Publishing AG
About this chapter
Cite this chapter
Gil-Pelegrín, E., Saz, M.Á., Cuadrat, J.M., Peguero-Pina, J.J., Sancho-Knapik, D. (2017). Oaks Under Mediterranean-Type Climates: Functional Response to Summer Aridity. In: Gil-Pelegrín, E., Peguero-Pina, J., Sancho-Knapik, D. (eds) Oaks Physiological Ecology. Exploring the Functional Diversity of Genus Quercus L.. Tree Physiology, vol 7. Springer, Cham. https://doi.org/10.1007/978-3-319-69099-5_5
Download citation
DOI: https://doi.org/10.1007/978-3-319-69099-5_5
Published:
Publisher Name: Springer, Cham
Print ISBN: 978-3-319-69098-8
Online ISBN: 978-3-319-69099-5
eBook Packages: Biomedical and Life SciencesBiomedical and Life Sciences (R0)