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The narrow-leaf syndrome: a functional and evolutionary approach to the form of fog-harvesting rosette plants

Abstract

Plants that use fog as an important water-source frequently have a rosette growth habit. The performance of this morphology in relation to fog interception has not been studied. Some first-principles from physics predict that narrow leaves, together with other ancillary traits (large number and high flexibility of leaves, caudices, and/or epiphytism) which constitute the “narrow-leaf syndrome” should increase fog-interception efficiency. This was tested using aluminum models of rosettes that differed in leaf length, width and number and were exposed to artificial fog. The results were validated using seven species of Tillandsia and four species of xerophytic rosettes. The total amount of fog intercepted in rosette plants increased with total leaf area, while narrow leaves maximized interception efficiency (measured as interception per unit area). The number of leaves in the rosettes is physically constrained because wide-leafed plants can only have a few blades. At the limits of this constraint, net fog interception was independent of leaf form, but interception efficiency was maximized by large numbers of narrow leaves. Atmospheric Tillandsia species show the narrow-leaf syndrome. Their fog interception efficiencies were correlated to the ones predicted from aluminum-model data. In the larger xerophytic rosette species, the interception efficiency was greatest in plants showing the narrow-leaf syndrome. The adaptation to fog-harvesting in several narrow-leaved rosettes was tested for evolutionary convergence in 30 xerophytic rosette species using a comparative method. There was a significant evolutionary tendency towards the development of the narrow-leaf syndrome the closer the species grew to areas where fog is frequently available. This study establishes convergence in a very wide group of plants encompassing genera as contrasting as Tillandsia and Agave as a result of their dependence on fog.

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References

  • Aigner DJ, Lovell CAK, Schmidt P (1977) Formulation and estimation of stochastic frontier production function models. J Econom 6:21–37

    Article  Google Scholar 

  • Benzing DH (1990) Vascular epiphytes. General biology and related biota. Cambridge University Press, Cambridge

    Google Scholar 

  • Boucher JF, Munson AD, Bernier PY (1995) Foliar absorption of dew influences shoot water potential and root growth in Pinus strobus seedlings. Tree Physiol 15:819–823

    Google Scholar 

  • Cavelier J, Goldstein G (1989) Mist and fog interception in elfin cloud forests in Colombia and Venezuela. J Trop Ecol 5:309–322

    Article  Google Scholar 

  • Cochran WG, Cox GM (1957) Experimental designs, 2nd edn. Wiley, New York

    Google Scholar 

  • Coddington JA (1994) The roles of homology and convergence in studies of adaptation. In: Eggleton P, Vane-Wright RI (eds) Phylogenetics and ecology. Academic, London, pp 53–78

    Google Scholar 

  • Coelli TJ (1996) A Guide to FRONTIER version 4.1: a computer program for stochastic frontier production and cost function estimation. CEPA Working Paper 96/7, Department of Econometrics, University of New England, Armidale, NSW, Australia

  • Crawley MJ (1993) GLIM for ecologists. Blackwell, Oxford

    Google Scholar 

  • Crayn DM, Winter K, Smith AC (2004) Multiple origins of crassulacean acid metabolism and the epiphytic habit in the neotropical family Bromeliaceae. Proc Natl Acad Sci USA 101:3703–3708

    Google Scholar 

  • Dawson TE (1998) Fog in the California redwood forest: ecosystem inputs and use by plants. Oecologia 117:476–485

    Google Scholar 

  • Gentry HS (1982) Agaves of Continental North America. University of Arizona Press, Tucson

    Google Scholar 

  • Gilmartin AJ (1983) Evolution of mesic and xeric habits in Tillandsia and Vriesea (Bromeliaceae). Syst Bot 8:233–242

    Article  Google Scholar 

  • Harvey PH, Pagel MD (1991) The comparative method in evolutionary ecology. Oxford University Press, Oxford

    Google Scholar 

  • Huey RB, Bennett AF (1986) A comparative approach to field and laboratory studies in evolutionary biology In: Feder ME, Lauder GV (eds) Predator-prey relationships: perspectives and approaches for the study of lower vertebrates. University of Chicago Press, Chicago, pp 82–96

    Google Scholar 

  • Jackson DA (1993) Principal component analysis: how many components are nontrivial and interpretable? Ecology 74:2204–2214

    Article  Google Scholar 

  • Jones HG (1992) Plants and microclimate. A quantitative approach to environmental plant physiology, 2nd edn. Cambridge University Press, Cambridge

    Google Scholar 

  • Kürschner H, Frey W (1999) Patterns and adaptive trends of life forms, life strategies, and ecomorphological structures in tropical epiphytic bryophytes – a pantropical synopsis. Nova Hedwigia 69:73–99

    Google Scholar 

  • Kürschner H, Parolly G (1998) Lebensformen und adaptationen zur wasserleitung und wasserspeicherung in epiphytischen moosgesellschaften Nord-Perus (Amazonas-Tiefland, Cordillera Oriental, Cordillera Central). Nova Hedwigia 67:349–379

    Google Scholar 

  • Larson DW (1981) Differential wetting in some lichens and mosses: the role of morphology. Bryologist 84:1–15

    Article  Google Scholar 

  • Leyton L, Armitage LP (1968) Cuticle structure and water relations of the needles of Pinus radiata (D. Don). New Phytol 67:31–38

    Article  Google Scholar 

  • Mabberley DJ (1986) Adaptive syndromes of the Afroalpine species of Dendrosenecio. In: Vuilleumier F, Monasterio M (eds) High altitude tropical biogeography. Oxford University Press, New York, pp 81–102

    Google Scholar 

  • Mandujano M (2001) El collar marcescente de Yucca periculosa: Una característica adaptativa a la aridez. B.Sc thesis, Universidad Nacional Autónoma de México, Mexico DF

  • Martin CE (1994) Physiological ecology of the Bromeliaceae. Bot Rev 60:1–82

    Google Scholar 

  • Martorell C (2002) Morfología funcional de la rosetofilia: ¿Plantas que cosechan la neblina? PhD thesis, Universidad Nacional Autónoma de México, Mexico DF

  • Martorell C, Ezcurra E (2002) Rosette scrub occurrence and fog availability in arid mountains of Mexico. J Veg Sci 13:651–662

    Article  Google Scholar 

  • Mez C (1904) Physiologische Bromeliaceen-Studien. I. Die wasser-ökonomie der extrem atmosphärischen Tillandsien. Jahrb Wiss Bot 40:157–229

    Google Scholar 

  • Mooney HA, Weisser PJ, Gulmon SL (1977) Environmental adaptations of the Atacaman Desert cactus Copiapoa haseltoniana. Flora 166:117–124

    Google Scholar 

  • Nobel PS (1988) Physicochemical and environmental plant physiology. Academic, San Diego

    Google Scholar 

  • Pagel MD (1994) The adaptationist wager. In: Eggleton P, Vane-Wright RI (eds) Phylogenetics and ecology. Academic, London, pp 29–52

    Google Scholar 

  • Ramírez de Arellano F (1996) Escurrimiento caulinar y eficiencia arquitectónica para la captación de agua en cinco especies de plantas del Valle de Zapotitlán Salinas, Puebla. B.Sc thesis, Universidad Nacional Autónoma de México, Mexico DF

    Google Scholar 

  • Rundel PW, Dillon MO (1998) Ecological patterns in the Bromeliaceae of the lomas formations of coastal Chile and Peru. Plant Syst Evol 212:261–278

    Google Scholar 

  • Rundel PW, Dillon MO, Palma B, Mooney HA, Gulmon SL, Ehleringer JR (1991) The phytogeography and ecology of the coastal Atacama and Peruvian deserts. Aliso 13:1–49

    Google Scholar 

  • Rundel PW, Mahu M (1976) Community structure and diversity in a coastal fog desert in northern Chile. Flora 165:493–505

    Google Scholar 

  • Smith LB, Downs RJ (1974) Pitcairnioideae (Bromeliaceae). Hafner Press, New York

    Google Scholar 

  • Trevelyan R, Harvey PH, Pagel MD (1990) Metabolic rates and life histories in birds. Funct Ecol 4:135–141

    Article  Google Scholar 

  • Wainwright PC (1994) Functional morphology as a tool in ecological research. In: Wainwright PC, Reilly SM (eds) Ecological morphology. Integrative organismal biology. University of Chicago Press, Chicago, pp 42–59

    Google Scholar 

  • Welty JR, Wicks CE, Wilson RE (1984) Fundamentals of momentum, heat, and mass transfer, 3rd edn. Wiley, New York

    Google Scholar 

  • Wenzel JW, Carpenter JM (1994) Comparing methods: adaptive traits and tests of adaptation. In: Eggleton P, Vane-Wright RI (eds) Phylogenetics and ecology. Academic, London, pp 79–102

    Google Scholar 

  • Woodhouse RM, Williams JG, Nobel PS (1980) Leaf orientation, radiation interception, and nocturnal acidity increases by the CAM plant Agave deserti (Agavaceae). Am J Bot 67:1179–1185

    Article  Google Scholar 

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Acknowledgments

We are grateful to Drs. M. Franco, A. Flores, L.E. Eguiarte, F. Molina, C. Montaña, P. Ramsey, A. Zavala and three anonymous reviewers for their valuable comments on the early versions of the manuscript. Edward Peters and Andrea Martínez helped in the design of the aluminum models and in the fog simulations. Pavka Patiño assisted us with the analysis of plant morphology through photographs. The Consejo Nacional de Ciencia y Tecnología (CONACyT) supported the first author with a PhD scholarship.

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Correspondence to Carlos Martorell.

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Communicated by Todd Dawson.

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Martorell, C., Ezcurra, E. The narrow-leaf syndrome: a functional and evolutionary approach to the form of fog-harvesting rosette plants. Oecologia 151, 561–573 (2007). https://doi.org/10.1007/s00442-006-0614-x

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