Leaf traits and herbivore selection in the field and in cafeteria experiments

Despite the vast diversity and complexity of herbivores, plants and their interactions, most authors agree that a small number of components of leaf quality affect preference by generalist herbivores in a predictable way. However, herbivore preference is determined not only by intrinsic plant attrib...

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Published inAustral ecology Vol. 28; no. 6; pp. 642 - 650
Main Authors Pérez-Harguindeguy, Natalia, Díaz, Sandra, Vendramini, Fernanda, Cornelissen, Johannes H. C., Gurvich, Diego E., Cabido, Marcelo
Format Journal Article
LanguageEnglish
Published Oxford, UK Blackwell Science Pty 01.12.2003
Blackwell
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Abstract Despite the vast diversity and complexity of herbivores, plants and their interactions, most authors agree that a small number of components of leaf quality affect preference by generalist herbivores in a predictable way. However, herbivore preference is determined not only by intrinsic plant attributes and herbivore biology but also by the environmental context. Within this framework, we aimed to analyse general interspecific trends in the association between herbivory and leaf traits over a wide range of angiosperms from central Argentina. We (i) tested for consistent associations between leaf traits, consumption in the field, and preference of generalist invertebrate herbivores in cafeteria experiments; (ii) assessed how well herbivore preferences in cafeterias matched leaf consumption in the field; and (iii) developed a simple conceptual model linking leaf traits, herbivore preference in cafeterias and consumption in the field. In general, we found that tender leaves with higher nutritional quality were preferred by herbivores, both in the field and in cafeteria experiments. According to our model, this relationship between field and cafeteria consumption and leaf quality is observed when generalist herbivores and plants of high accessibility are considered. However, differences between leaf consumption in the field and in cafeteria experiments can also be found. At least two reasons can account for this: (i) specialized plant–herbivore relationships often occur in the field, whereas cafeteria experiments tend to consider only one or a few generalist herbivores; (ii) different plant species growing in the field often differ in their degree of accessibility to herbivores, whereas in cafeteria experiments all species are equally accessible. Our results add new evidence to a growing consensus that, although herbivory in the field is determined by many factors, consistent patterns of differential susceptibility to foliar feeders can be found in leaves differing in nutritional quality and thus in resource‐use strategy.
AbstractList Despite the vast diversity and complexity of herbivores, plants and their interactions, most authors agree that a small number of components of leaf quality affect preference by generalist herbivores in a predictable way. However, herbivore preference is determined not only by intrinsic plant attributes and herbivore biology but also by the environmental context. Within this framework, we aimed to analyse general interspecific trends in the association between herbivory and leaf traits over a wide range of angiosperms from central Argentina. We (i) tested for consistent associations between leaf traits, consumption in the field, and preference of generalist invertebrate herbivores in cafeteria experiments; (ii) assessed how well herbivore preferences in cafeterias matched leaf consumption in the field; and (iii) developed a simple conceptual model linking leaf traits, herbivore preference in cafeterias and consumption in the field. In general, we found that tender leaves with higher nutritional quality were preferred by herbivores, both in the field and in cafeteria experiments. According to our model, this relationship between field and cafeteria consumption and leaf quality is observed when generalist herbivores and plants of high accessibility are considered. However, differences between leaf consumption in the field and in cafeteria experiments can also be found. At least two reasons can account for this: (i) specialized plant–herbivore relationships often occur in the field, whereas cafeteria experiments tend to consider only one or a few generalist herbivores; (ii) different plant species growing in the field often differ in their degree of accessibility to herbivores, whereas in cafeteria experiments all species are equally accessible. Our results add new evidence to a growing consensus that, although herbivory in the field is determined by many factors, consistent patterns of differential susceptibility to foliar feeders can be found in leaves differing in nutritional quality and thus in resource‐use strategy.
Abstract  Despite the vast diversity and complexity of herbivores, plants and their interactions, most authors agree that a small number of components of leaf quality affect preference by generalist herbivores in a predictable way. However, herbivore preference is determined not only by intrinsic plant attributes and herbivore biology but also by the environmental context. Within this framework, we aimed to analyse general interspecific trends in the association between herbivory and leaf traits over a wide range of angiosperms from central Argentina. We (i) tested for consistent associations between leaf traits, consumption in the field, and preference of generalist invertebrate herbivores in cafeteria experiments; (ii) assessed how well herbivore preferences in cafeterias matched leaf consumption in the field; and (iii) developed a simple conceptual model linking leaf traits, herbivore preference in cafeterias and consumption in the field. In general, we found that tender leaves with higher nutritional quality were preferred by herbivores, both in the field and in cafeteria experiments. According to our model, this relationship between field and cafeteria consumption and leaf quality is observed when generalist herbivores and plants of high accessibility are considered. However, differences between leaf consumption in the field and in cafeteria experiments can also be found. At least two reasons can account for this: (i) specialized plant–herbivore relationships often occur in the field, whereas cafeteria experiments tend to consider only one or a few generalist herbivores; (ii) different plant species growing in the field often differ in their degree of accessibility to herbivores, whereas in cafeteria experiments all species are equally accessible. Our results add new evidence to a growing consensus that, although herbivory in the field is determined by many factors, consistent patterns of differential susceptibility to foliar feeders can be found in leaves differing in nutritional quality and thus in resource‐use strategy.
Author Díaz, Sandra
Cornelissen, Johannes H. C.
Gurvich, Diego E.
Cabido, Marcelo
Vendramini, Fernanda
Pérez-Harguindeguy, Natalia
Author_xml – sequence: 1
  givenname: Natalia
  surname: Pérez-Harguindeguy
  fullname: Pérez-Harguindeguy, Natalia
  organization: 1 Instituto Multidisciplinario de Biología Vegetal (UNC-CONICET) and FCEFyN, Universidad Nacional de Córdoba, CC 495 Córdoba, Argentina (Email: nperez@com.uncor.edu), and 2Department of Systems Ecology, Institute of Ecological Sciences, Faculty of Earth and Life Science, Vrije Universiteit, Amsterdam, The Netherlands
– sequence: 2
  givenname: Sandra
  surname: Díaz
  fullname: Díaz, Sandra
  organization: 1 Instituto Multidisciplinario de Biología Vegetal (UNC-CONICET) and FCEFyN, Universidad Nacional de Córdoba, CC 495 Córdoba, Argentina (Email: nperez@com.uncor.edu), and 2Department of Systems Ecology, Institute of Ecological Sciences, Faculty of Earth and Life Science, Vrije Universiteit, Amsterdam, The Netherlands
– sequence: 3
  givenname: Fernanda
  surname: Vendramini
  fullname: Vendramini, Fernanda
  organization: 1 Instituto Multidisciplinario de Biología Vegetal (UNC-CONICET) and FCEFyN, Universidad Nacional de Córdoba, CC 495 Córdoba, Argentina (Email: nperez@com.uncor.edu), and 2Department of Systems Ecology, Institute of Ecological Sciences, Faculty of Earth and Life Science, Vrije Universiteit, Amsterdam, The Netherlands
– sequence: 4
  givenname: Johannes H. C.
  surname: Cornelissen
  fullname: Cornelissen, Johannes H. C.
  organization: 1 Instituto Multidisciplinario de Biología Vegetal (UNC-CONICET) and FCEFyN, Universidad Nacional de Córdoba, CC 495 Córdoba, Argentina (Email: nperez@com.uncor.edu), and 2Department of Systems Ecology, Institute of Ecological Sciences, Faculty of Earth and Life Science, Vrije Universiteit, Amsterdam, The Netherlands
– sequence: 5
  givenname: Diego E.
  surname: Gurvich
  fullname: Gurvich, Diego E.
  organization: 1 Instituto Multidisciplinario de Biología Vegetal (UNC-CONICET) and FCEFyN, Universidad Nacional de Córdoba, CC 495 Córdoba, Argentina (Email: nperez@com.uncor.edu), and 2Department of Systems Ecology, Institute of Ecological Sciences, Faculty of Earth and Life Science, Vrije Universiteit, Amsterdam, The Netherlands
– sequence: 6
  givenname: Marcelo
  surname: Cabido
  fullname: Cabido, Marcelo
  organization: 1 Instituto Multidisciplinario de Biología Vegetal (UNC-CONICET) and FCEFyN, Universidad Nacional de Córdoba, CC 495 Córdoba, Argentina (Email: nperez@com.uncor.edu), and 2Department of Systems Ecology, Institute of Ecological Sciences, Faculty of Earth and Life Science, Vrije Universiteit, Amsterdam, The Netherlands
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Issue 6
Keywords Trophic group
Carbon nitrogen ratio
Phytophagous
Animal plant relation
Nutritive value
Angiospermae
Spermatophyta
Plant leaf
Invertebrata
Feeding preference
Interspecific relation
Language English
License CC BY 4.0
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References Gallardo A. & Merino J. (1993) Leaf decomposition in two Mediterranean ecosystems of Southwest Spain: Influence of substrate quality. Ecology 74, 152-61.
Grubb P. J. (1992) A positive distrust in simplicity: Lessons from plant defences and from competition among plants and among animals. J. Ecol. 80, 585-610.
Tsingalia M. H. (1989) Variation in seedling predation and herbivory in Prunus africana in the Kakamega forest, Kenya. Afr. J. Ecol. 27, 207-17.
Crawley M. J. (1983) Herbivory: the Dynamics of Animal-Plant Interactions. Blackwell Scientific Publications, Oxford.
Fraser L. H. & Grime J. P. (1999) Aphid fitness on 13 grass species: A test of plant defence theory. Can. J. Bot. 77, 1783-9.
Aerts R. & Chapin F. S. III (2000) The mineral nutrition of wild plants revisited: A re-evaluation of processes and patterns. Adv. Ecol. Res. 30, 2-69.
Norusis M. J. (1992) SPSS for Windows Base System: User's Guide. Release 5.0. SPSS, Chicago.
Garnier E. & Laurent G. (1994) Leaf anatomy, specific mass and water content in congeneric annual and perennial grass species. New Phytol. 128, 725-36.
Grime J. P., Cornelissen J. H. C., Thompson K. & Hodgson J. G. (1996) Evidence of a causal connection between anti-herbivore defence and the decomposition rate of leaves. Oikos 77, 489-94.
Coley P. D. (1988) Effects of plant growth rate and leaf lifetime on the amount and type of antiherbivore defence. Oecologia 74, 531-6.
Pérez-Harguindeguy N., Díaz S., Cornelissen J. H. C., Vendramini F., Cabido M. & Castellanos A. (2000) Chemistry and toughness predict leaf litter decomposition rates over a wide spectrum of functional types and taxa in central Argentina. Plant Soil 218, 21-30.
Olff H., Vera F. W. M., Bokdam J. et al. (1999) Associational resistance of plants to herbivory may lead to shifting mosaics in grazed woodlands. Plant Biol. 1, 127-37.
Cornelissen J. H. C., Werger M. J. A., Castro-Díez P., Van Rheenen J. W. A. & Rowland A. P. (1997) Foliar nutrients in relation to growth, allocation and leaf traits in seedlings of a wide range of woody plant species and types. Oecologia 111, 460-9.
Díaz S. & Cabido M. (1997) Plant functional types and ecosystem function in response to global change: A multiscale approach. J. Veg. Sci. 8, 463-74.
Scriber J. M. & Feeny P. (1979) Growth of herbivorous caterpillars in relation to feeding specialization and to the growth form of their food plants. Ecology 60, 829-50.
Lawler I. R., Foley W. J. & Eschler B. M. (2000) Foliar concentration of a single toxin creates habitat patchiness for a marsupial folivore. Ecology 81, 1327-38.
Scheidel U. & Bruelheide H. (1999) Selective slug grazing on montane meadow plants. J. Ecol. 87, 828-38.
Westoby M., Falster D., Moles A., Vesk P. & Wright I. (2002) Plant ecological strategies: Some leading dimensions of variation between species. Ann. Rev. Ecol. Syst. 33, 125-59.
Feeny P. (1990) Theories of plant-chemical defence: A brief historical summary. Symp. Biol. Hung. 89, 163-75.
Hanley M. E. & Lamont B. B. (2002) Relationships between physical and chemical attributes of congeneric seedlings: How important is seedling defence? Funct. Ecol. 16, 216-22.
Soltis P. S., Soltis D. E., Zanis M. J. & Kim S. (2000) Basal lineages of Angiosperms: Relationships and implications for floral evolution. Int. J. Plant. Sci. 1616 (Suppl.), S97-S107.
Herms D. A. & Mattson W. J. (1992) The dilemma of plants: To growth or defend? Quart. Rev. Biol. 67, 283-335.
Chapin F. S. III, Autumn K. & Pugnaire F. (1993) Evolution of suites of traits in response to environmental stress. Am. Nat. 142, 78-92.
Singer M. C. (2000) Reducing ambiguity in describing plant-insect interactions: 'preference', 'acceptability' and 'electivity'. Ecol. Lett. 3, 159-62.
Scriber J. M. (1977) Limiting effects of low leaf-water content on the nitrogen utilization, energy budget and larval growth of Hyalophora cecropia (Lepidotera: Saturniidae). Oecologia 28, 269-87.
Vendramini F., Díaz S., Pérez-Harguindeguy N., Cabido M., Llano-Sotelo J. M. & Castellanos A. (2000) Composición química y caracteres foliares en plantas de distintos tipos funcionales del centro-oeste de Argentina. Kurtziana 28, 181-93.
Feeny P. (1970) Seasonal changes in oak leaf tannins and nutrients as a cause of spring feeding by winter moth caterpillars. Ecology 51, 565-81.
Tribe D. E. (1959) The behaviour of the grazing animal: A critical review of present knowledge. J. Br. Grassl. Soc. 5, 200-14.
Lambers H. & Poorter H. (1992) Inherent variation in growth rate between higher plants: A search for physiological causes and ecological consequences. Adv. Ecol. Res. 23, 188-242.
McClaugherty C. A., Pastor J., Aber J. D. & Melillo J. M. (1985) Forest litter decomposition in relation to soil nitrogen dynamics and litter quality. Ecology 66, 266-75.
Wardle D. A., Barker G. M., Bonner K. I. & Nicholson K. S. (1998) Can comparative approaches based on plant ecophysiological traits predict the nature of biotic interactions and individual plant species effects in ecosystems? J. Ecol. 86, 405-20.
Westerbergh A. & Nyberg A. B. (1995) Selective grazing of hairless Silene dioica plants by land gastropods. Oikos 73, 216-22.
Huntly N. (1991) Herbivores and the dynamics of communities and ecosystems. Annu. Rev. Ecol. Syst. 22, 477-503.
Shipley B. (1995) Structured interspecific determinants of specific leaf area in 34 species of herbaceous angiosperms. Funct. Ecol. 9, 312-19.
Cornelissen J. H. C., Castro-Díez P. & Hunt R. (1996) Seedling growth, allocation and leaf attributes in a wide range of woody plant species and types. J. Ecol. 84, 755-65.
Grime J. P. (2001) Plant Strategies, Vegetation Processes, and Ecosystem Properties. John Wiley & Sons, Chichester.
Choat J. H. & Clements K. D. (1998) Vertebrate herbivores in marine and terrestrial environments: A nutritional perspective. Annu. Rev. Ecol. Syst. 29, 375-403.
Godan D. (1983) Pest Slugs and Snails: Ecology and Control. Springer, Berlin.
Mattson W. J. Jr (1980) Herbivory in relation to plant nitrogen content. Ann. Rev. Ecol. Syst. 11, 119-61.
Schlesinger W. H. (1977) Carbon balance in terrestrial detritus. Annu. Rev. Ecol. Syst. 8, 51-81.
Dirzo R. (1980) Experimental studies on slug-plant interactions. 1. The acceptability of thirty plant species to the slug Agriolimax carunae. J. Ecol. 68, 981-98.
Gastón J. (1969) Síntesis histórica de las invasiones de langosta en la Argentina. Secretaría Estado Agricultura y Ganadería. Pub. Misc. 433, 1-30.
Tabashnik B. E. (1982) Responses of pest and non-pest Colias butterfly larvae to intraspecific variation in leaf nitrogen and water content. Oecologia 55, 389-94.
Cornelissen J. H. C., Pérez-Harguindeguy N., Díaz S. et al. (1999) Leaf structure and defence control litter decomposition rate across species and life forms in regional floras of two continents. New Phytol. 143, 191-200.
Hendry G. A. F. & Grime J. P. (1993) Methods in Comparative Plant Ecology. Chapman & Hall, London.
Diaz S., Noy-Meir I. & Cabido M. (2001) Can grazing response to herbaceous plants be predicted from simple vegetative traits? J. Appl. Ecol. 38, 497-508.
Hollander M. & Wolfe D. A. (1972) Non Parametric Statistical Methods. John Wiley and Sons, New York.
Karban R., Agrawal A. A., Thaler J. S. & Adler L. S. (1999) Induced plant responses and information content about risk of herbivory. Trends Ecol. Evol. 14, 443-7.
Cunningham S. A., Summerhayes B. & Westoby M. (1999) Evolutionary divergences in leaf structure and chemistry, comparing rainfall and soil nutrient gradients. Ecology 69, 569-88.
Fraser L. H. (1996) Top-down vs. bottom-up control influenced by productivity in a North Derbyshire, UK, dale. Oikos 81, 99-108.
Garnier E., Cordonnier P., Guillerm J.-L. & Sonnié L. (1997) Specific leaf area and leaf nitrogen concentration in annual and perennial grass species growing in Mediterranean old-fields. Oecologia 111, 490-8.
Krebs C. J. (1989) Ecological Methodology. Harper & Row Publishers, New York.
Coley P. D., Bryant J. P. & Chapin F. S. III (1985) Resource availability and plant antiherbivore defense. Science 230, 895-9.
Díaz S., Cabido M. & Casanoves F. (1998) Functional traits and environmental filters at a regional scale. J. Veg. Sci. 9, 113-22.
Wilson P. J., Thompson K. & Hodgson J. G. (1999) Specific leaf area and leaf dry matter content as alternative predictors of plant strategies. New Phytol. 143, 55-162.
2002; 16
1995; 73
1977; 28
2000; 3
1997; 111
2000; 218
1982; 55
1999; 87
1972
2000; 1616
1988; 74
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1985; 66
1998; 86
1979
1997; 8
1996; 77
1959; 5
1990; 89
2001
1993; 74
1999; 14
1983
1979; 60
1989
1995; 9
1998; 29
1992; 80
2000; 28
1980; 68
1999; 69
2002; 33
1999; 143
1997
1970; 51
1993
1992
1999; 1
1989; 27
1993; 142
1999
1994; 128
1991; 22
2000; 30
1980; 11
1999; 77
2000; 81
1996; 84
2001; 38
1996; 81
1969; 433
1992; 67
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References_xml – reference: Krebs C. J. (1989) Ecological Methodology. Harper & Row Publishers, New York.
– reference: Garnier E. & Laurent G. (1994) Leaf anatomy, specific mass and water content in congeneric annual and perennial grass species. New Phytol. 128, 725-36.
– reference: Fraser L. H. (1996) Top-down vs. bottom-up control influenced by productivity in a North Derbyshire, UK, dale. Oikos 81, 99-108.
– reference: Cornelissen J. H. C., Castro-Díez P. & Hunt R. (1996) Seedling growth, allocation and leaf attributes in a wide range of woody plant species and types. J. Ecol. 84, 755-65.
– reference: Tabashnik B. E. (1982) Responses of pest and non-pest Colias butterfly larvae to intraspecific variation in leaf nitrogen and water content. Oecologia 55, 389-94.
– reference: McClaugherty C. A., Pastor J., Aber J. D. & Melillo J. M. (1985) Forest litter decomposition in relation to soil nitrogen dynamics and litter quality. Ecology 66, 266-75.
– reference: Schlesinger W. H. (1977) Carbon balance in terrestrial detritus. Annu. Rev. Ecol. Syst. 8, 51-81.
– reference: Cornelissen J. H. C., Werger M. J. A., Castro-Díez P., Van Rheenen J. W. A. & Rowland A. P. (1997) Foliar nutrients in relation to growth, allocation and leaf traits in seedlings of a wide range of woody plant species and types. Oecologia 111, 460-9.
– reference: Feeny P. (1990) Theories of plant-chemical defence: A brief historical summary. Symp. Biol. Hung. 89, 163-75.
– reference: Scriber J. M. & Feeny P. (1979) Growth of herbivorous caterpillars in relation to feeding specialization and to the growth form of their food plants. Ecology 60, 829-50.
– reference: Soltis P. S., Soltis D. E., Zanis M. J. & Kim S. (2000) Basal lineages of Angiosperms: Relationships and implications for floral evolution. Int. J. Plant. Sci. 1616 (Suppl.), S97-S107.
– reference: Cornelissen J. H. C., Pérez-Harguindeguy N., Díaz S. et al. (1999) Leaf structure and defence control litter decomposition rate across species and life forms in regional floras of two continents. New Phytol. 143, 191-200.
– reference: Godan D. (1983) Pest Slugs and Snails: Ecology and Control. Springer, Berlin.
– reference: Westoby M., Falster D., Moles A., Vesk P. & Wright I. (2002) Plant ecological strategies: Some leading dimensions of variation between species. Ann. Rev. Ecol. Syst. 33, 125-59.
– reference: Chapin F. S. III, Autumn K. & Pugnaire F. (1993) Evolution of suites of traits in response to environmental stress. Am. Nat. 142, 78-92.
– reference: Scheidel U. & Bruelheide H. (1999) Selective slug grazing on montane meadow plants. J. Ecol. 87, 828-38.
– reference: Singer M. C. (2000) Reducing ambiguity in describing plant-insect interactions: 'preference', 'acceptability' and 'electivity'. Ecol. Lett. 3, 159-62.
– reference: Scriber J. M. (1977) Limiting effects of low leaf-water content on the nitrogen utilization, energy budget and larval growth of Hyalophora cecropia (Lepidotera: Saturniidae). Oecologia 28, 269-87.
– reference: Shipley B. (1995) Structured interspecific determinants of specific leaf area in 34 species of herbaceous angiosperms. Funct. Ecol. 9, 312-19.
– reference: Feeny P. (1970) Seasonal changes in oak leaf tannins and nutrients as a cause of spring feeding by winter moth caterpillars. Ecology 51, 565-81.
– reference: Coley P. D. (1988) Effects of plant growth rate and leaf lifetime on the amount and type of antiherbivore defence. Oecologia 74, 531-6.
– reference: Coley P. D., Bryant J. P. & Chapin F. S. III (1985) Resource availability and plant antiherbivore defense. Science 230, 895-9.
– reference: Gallardo A. & Merino J. (1993) Leaf decomposition in two Mediterranean ecosystems of Southwest Spain: Influence of substrate quality. Ecology 74, 152-61.
– reference: Grime J. P. (2001) Plant Strategies, Vegetation Processes, and Ecosystem Properties. John Wiley & Sons, Chichester.
– reference: Tsingalia M. H. (1989) Variation in seedling predation and herbivory in Prunus africana in the Kakamega forest, Kenya. Afr. J. Ecol. 27, 207-17.
– reference: Lambers H. & Poorter H. (1992) Inherent variation in growth rate between higher plants: A search for physiological causes and ecological consequences. Adv. Ecol. Res. 23, 188-242.
– reference: Hendry G. A. F. & Grime J. P. (1993) Methods in Comparative Plant Ecology. Chapman & Hall, London.
– reference: Huntly N. (1991) Herbivores and the dynamics of communities and ecosystems. Annu. Rev. Ecol. Syst. 22, 477-503.
– reference: Herms D. A. & Mattson W. J. (1992) The dilemma of plants: To growth or defend? Quart. Rev. Biol. 67, 283-335.
– reference: Hollander M. & Wolfe D. A. (1972) Non Parametric Statistical Methods. John Wiley and Sons, New York.
– reference: Karban R., Agrawal A. A., Thaler J. S. & Adler L. S. (1999) Induced plant responses and information content about risk of herbivory. Trends Ecol. Evol. 14, 443-7.
– reference: Gastón J. (1969) Síntesis histórica de las invasiones de langosta en la Argentina. Secretaría Estado Agricultura y Ganadería. Pub. Misc. 433, 1-30.
– reference: Grime J. P., Cornelissen J. H. C., Thompson K. & Hodgson J. G. (1996) Evidence of a causal connection between anti-herbivore defence and the decomposition rate of leaves. Oikos 77, 489-94.
– reference: Westerbergh A. & Nyberg A. B. (1995) Selective grazing of hairless Silene dioica plants by land gastropods. Oikos 73, 216-22.
– reference: Olff H., Vera F. W. M., Bokdam J. et al. (1999) Associational resistance of plants to herbivory may lead to shifting mosaics in grazed woodlands. Plant Biol. 1, 127-37.
– reference: Díaz S. & Cabido M. (1997) Plant functional types and ecosystem function in response to global change: A multiscale approach. J. Veg. Sci. 8, 463-74.
– reference: Dirzo R. (1980) Experimental studies on slug-plant interactions. 1. The acceptability of thirty plant species to the slug Agriolimax carunae. J. Ecol. 68, 981-98.
– reference: Pérez-Harguindeguy N., Díaz S., Cornelissen J. H. C., Vendramini F., Cabido M. & Castellanos A. (2000) Chemistry and toughness predict leaf litter decomposition rates over a wide spectrum of functional types and taxa in central Argentina. Plant Soil 218, 21-30.
– reference: Díaz S., Cabido M. & Casanoves F. (1998) Functional traits and environmental filters at a regional scale. J. Veg. Sci. 9, 113-22.
– reference: Cunningham S. A., Summerhayes B. & Westoby M. (1999) Evolutionary divergences in leaf structure and chemistry, comparing rainfall and soil nutrient gradients. Ecology 69, 569-88.
– reference: Norusis M. J. (1992) SPSS for Windows Base System: User's Guide. Release 5.0. SPSS, Chicago.
– reference: Wilson P. J., Thompson K. & Hodgson J. G. (1999) Specific leaf area and leaf dry matter content as alternative predictors of plant strategies. New Phytol. 143, 55-162.
– reference: Aerts R. & Chapin F. S. III (2000) The mineral nutrition of wild plants revisited: A re-evaluation of processes and patterns. Adv. Ecol. Res. 30, 2-69.
– reference: Garnier E., Cordonnier P., Guillerm J.-L. & Sonnié L. (1997) Specific leaf area and leaf nitrogen concentration in annual and perennial grass species growing in Mediterranean old-fields. Oecologia 111, 490-8.
– reference: Hanley M. E. & Lamont B. B. (2002) Relationships between physical and chemical attributes of congeneric seedlings: How important is seedling defence? Funct. Ecol. 16, 216-22.
– reference: Fraser L. H. & Grime J. P. (1999) Aphid fitness on 13 grass species: A test of plant defence theory. Can. J. Bot. 77, 1783-9.
– reference: Diaz S., Noy-Meir I. & Cabido M. (2001) Can grazing response to herbaceous plants be predicted from simple vegetative traits? J. Appl. Ecol. 38, 497-508.
– reference: Lawler I. R., Foley W. J. & Eschler B. M. (2000) Foliar concentration of a single toxin creates habitat patchiness for a marsupial folivore. Ecology 81, 1327-38.
– reference: Vendramini F., Díaz S., Pérez-Harguindeguy N., Cabido M., Llano-Sotelo J. M. & Castellanos A. (2000) Composición química y caracteres foliares en plantas de distintos tipos funcionales del centro-oeste de Argentina. Kurtziana 28, 181-93.
– reference: Mattson W. J. Jr (1980) Herbivory in relation to plant nitrogen content. Ann. Rev. Ecol. Syst. 11, 119-61.
– reference: Tribe D. E. (1959) The behaviour of the grazing animal: A critical review of present knowledge. J. Br. Grassl. Soc. 5, 200-14.
– reference: Grubb P. J. (1992) A positive distrust in simplicity: Lessons from plant defences and from competition among plants and among animals. J. Ecol. 80, 585-610.
– reference: Crawley M. J. (1983) Herbivory: the Dynamics of Animal-Plant Interactions. Blackwell Scientific Publications, Oxford.
– reference: Choat J. H. & Clements K. D. (1998) Vertebrate herbivores in marine and terrestrial environments: A nutritional perspective. Annu. Rev. Ecol. Syst. 29, 375-403.
– reference: Wardle D. A., Barker G. M., Bonner K. I. & Nicholson K. S. (1998) Can comparative approaches based on plant ecophysiological traits predict the nature of biotic interactions and individual plant species effects in ecosystems? J. Ecol. 86, 405-20.
– start-page: 223
  year: 1979
  end-page: 45
– volume: 86
  start-page: 405
  year: 1998
  end-page: 20
  article-title: Can comparative approaches based on plant ecophysiological traits predict the nature of biotic interactions and individual plant species effects in ecosystems?
  publication-title: J. Ecol.
– volume: 30
  start-page: 2
  year: 2000
  end-page: 69
  article-title: The mineral nutrition of wild plants revisited: A re‐evaluation of processes and patterns
  publication-title: Adv. Ecol. Res.
– volume: 23
  start-page: 188
  year: 1992
  end-page: 242
  article-title: Inherent variation in growth rate between higher plants: A search for physiological causes and ecological consequences
  publication-title: Adv. Ecol. Res.
– volume: 8
  start-page: 51
  year: 1977
  end-page: 81
  article-title: Carbon balance in terrestrial detritus
  publication-title: Annu. Rev. Ecol. Syst.
– volume: 9
  start-page: 113
  year: 1998
  end-page: 22
  article-title: Functional traits and environmental filters at a regional scale
  publication-title: J. Veg. Sci.
– volume: 89
  start-page: 163
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Snippet Despite the vast diversity and complexity of herbivores, plants and their interactions, most authors agree that a small number of components of leaf quality...
Abstract  Despite the vast diversity and complexity of herbivores, plants and their interactions, most authors agree that a small number of components of leaf...
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SubjectTerms Angiospermae
Animal and plant ecology
Animal, plant and microbial ecology
Argentina
Autoecology
Biological and medical sciences
carbon
comparative ecology
Fundamental and applied biological sciences. Psychology
herbivores
invertebrates
leaf toughness
leaves
nitrogen
nutritive value
plant functional traits
Plants and fungi
Synecology
Terrestrial ecosystems
Title Leaf traits and herbivore selection in the field and in cafeteria experiments
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Volume 28
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