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6 - Dimensions of plant disease in tropical forests

Published online by Cambridge University Press:  25 August 2009

By
Gregory S. Gilbert
Edited by
David Burslem ,
Michelle Pinard  and
Sue Hartley
Gregory S. Gilbert
Affiliation:
University of California, Santa Cruz and Smithsonian Tropical Research Institute, Balboa
David Burslem
Affiliation:
University of Aberdeen
Michelle Pinard
Affiliation:
University of Aberdeen
Sue Hartley
Affiliation:
University of Sussex
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Summary

Introduction

Pest pressure is the inevitable, ubiquitous factor in evolution which makes for an apparently pointless multiplicity of species in all areas in which it has time to operate.

(Gillett 1962)

At a symposium 44 years ago, J. B. Gillett proposed the Theory of Pest Pressure, whereby plant pathogens and pests were responsible for the genesis and maintenance of high plant diversity in tropical forests and other high-diversity systems. In his conclusion to the paper produced from that talk he hoped that this ‘new theory may be useful in stimulating discussion and research’ on the roles of pests and pathogens as a force in plant diversity. Apparently his theory has been useful, as much has happened in the last four decades to explore and expand on his idea. My aim is to review key research on the effects of plant pathogens in tropical forests since Gillett's seminal paper with emphasis on the special case of his Theory of Pest Pressure known as the Janzen–Connell Hypothesis. I will also suggest critical areas that need to be explored as we continue to discuss and research the role of pathogens in the maintenance of species diversity in tropical forests.

‘Parcere subiectis et debellare superbos’

Gillett (1962) paraphrased Virgil's famous formula for the greatness of Rome, ‘Spare the lowly and conquer the haughty’ (AeneidVI: 853), when he first introduced the idea that if plant pests have a greater impact on more common species than on rare species, the rare species should then increase in relative frequency, providing a mechanism for the maintenance of diversity in species-rich communities.

Type
Chapter
Information
Biotic Interactions in the Tropics
Their Role in the Maintenance of Species Diversity
 , pp. 141 - 164
Publisher: Cambridge University Press
Print publication year: 2005

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References

Alexander, H. M. & Antonovics, J.. 1988. Disease spread and population dynamics of anther-smut infection of Silene alba caused by the fungus Ustilago violacea. Journal of Ecology 76: 91–104CrossRefGoogle Scholar
Alexander, H. M. & Holt, R. D.. 1998. The interaction between plant competition and disease. Perspectives in Plant Ecology Evolution and Systematics 1: 206–220CrossRefGoogle Scholar
Alexander, S. A., Skelly, J. M. & Webb, R. S.. 1981. Effects of Heterobasidion annosum on radial growth in southern pine beetle-infested loblolly pine. Phytopathology 71: 479–481CrossRefGoogle Scholar
Anderson, R. C., Gardner, D. E., Daehler, C. C. & Meinzer, F. C.. 2001. Dieback of Acacia koa in Hawaii: ecological and pathological characteristics of affected stands. Forest Ecology and Management 5576: 1–14Google Scholar
Anthony, P. A., Holtum, J. A. M. & Jackes, B. R.. 2002. Shade acclimation of rainforest leaves to colonization by lichens. Functional Ecology 16: 808–816CrossRefGoogle Scholar
Arnold, A. E., Maynard, Z. & Gilbert, G. S.. 2001. Fungal endophytes in dicotyledonous neotropical trees: patterns of abundance and diversity. Mycological Research 105: 1502–1507CrossRefGoogle Scholar
Arnold, A. E., Maynard, Z., Gilbert, G. S., Coley, P. D. & Kursar, T. A.. 2000. Are tropical fungal endophytes hyperdiverse?Ecology Letters 3: 267–274CrossRefGoogle Scholar
Arthur, J. C. & Cummings, G. B.. 1933. New species of Uredinales. Annales Mycologica 31: 41Google Scholar
Augspurger, C. K. 1983a. Offspring recruitment around tropical trees – changes in cohort distance with time. Oikos 40: 189–196CrossRefGoogle Scholar
Augspurger, C. K. 1983b. Seed dispersal of the tropical tree, Platypodium elegans, and the escape of its seedlings from fungal pathogens. Journal of Ecology 71: 759–771CrossRefGoogle Scholar
Augspurger, C. K. 1984. Seedling survival of tropical tree species – interactions of dispersal distance, light-gaps, and pathogens. Ecology 65: 1705–1712CrossRefGoogle Scholar
Augspurger, C. K. 1990. Spatial patterns of damping-off disease during seedling recruitment in tropical forests. In , J. J. Burdon & , S. R. Leather, eds., Pests, Pathogens, and Plant Communities. Oxford: Blackwell Scientific Publications, pp. 131–144Google Scholar
Augspurger, C. K. & Kelly, C. K.. 1984. Pathogen mortality of tropical tree seedlings: experimental studies of the effects of dispersal distance, seedling density, and light conditions. Oecologia 61: 211–217CrossRefGoogle ScholarPubMed
Barone, J. A. 1998. Host-specificity of folivorous insects in a moist tropical forest. Journal of Animal Ecology 67: 400–409CrossRefGoogle Scholar
Bayman, P., Angulo-Sandoval, P., Báez-Ortiz, Z. & Lodge, D. J.. 1998. Distribution and dispersal of Xylaria endophytes in two tree species in Puerto Rico. Mycological Research 102: 944–948CrossRefGoogle Scholar
Bayman, P., Lebron, L. L., Tremblay, R. L. & Lodge, D. J.. 1997. Variation in endophytic fungi from roots and leaves of Lepanthes (Orchidaceae). New Phytologist 135: 143–149CrossRefGoogle Scholar
Bella, I. E. & Navratil, S.. 1988. Western gall rust dynamics and impact in young lodgepole pine stands in west-central Alberta. Canadian Journal of Forest Research 18: 1437–1442CrossRefGoogle Scholar
Benitez-Malvido, J., García-Guzman, G. & Kossmann-Ferraz, I. D.. 1999. Leaf-fungal incidence and herbivory on tree seedlings in tropical rainforest fragments: an experimental study. Biological Conservation 91: 143–150CrossRefGoogle Scholar
Bethancourt, E. 2000. Un método de muestreo para el estudio de la diversidad de hongos endófitos asociado a especies arbóreas en un bosque tropical. Unpublished Master's thesis, Universidad Tecnológica de Panamá
Bever, J. D. 1994. Feedback between plants and their soil communities in an old field community. Ecology 75: 1965–1977CrossRefGoogle Scholar
Bever, J. D., Westover, K. M. & Antonovics, J.. 1997. Incorporating the soil community into plant population dynamics: the utility of the feedback approach. Journal of Ecology 85: 561–573CrossRefGoogle Scholar
Bills, G. F. & Polishook, J. D.. 1994. Abundance and diversity of microfungi in leaf litter of a lowland rain forest in Costa Rica. Mycologia 86: 187–198CrossRefGoogle Scholar
Bloomberg, W. J. & Morrison, D. J.. 1989. Relationship of growth reduction in Douglas-fir to infection by Armillaria root disease in southeastern British Columbia [Canada]. Phytopathology 79: 482–487CrossRefGoogle Scholar
Bradley, D. J., Gilbert, G. S. & Parker, I. M.. 2003. Susceptibility of clover species to fungal infection: the interaction of leaf surface traits and environment. American Journal of Botany 90: 857–864CrossRefGoogle Scholar
Burdon, J. J. & Chilvers, G. A.. 1982. Host density as a factor in plant disease ecology. Annual Review of Phytopathology 20: 143–166CrossRefGoogle Scholar
Burdon, J. J. & Jarosz, A. M.. 1991. Host-pathogen interactions in natural populations of Linum marginale and Melampsora lini. 1. Patterns of resistance and racial variation in a large host population. Evolution 45: 205–217Google Scholar
Cannon, P. F. & Hawksworth, D. L.. 1995. The diversity of fungi associated with vascular plants: the known, the unknown and the need to bridge the knowledge gap. Advances in Plant Pathology 11: 277–302CrossRefGoogle Scholar
Carlsson-Graner, U. 1997. Anther-smut disease in Silene dioica: variation in susceptibility among genotypes and populations, and patterns of disease within populations. Evolution 51: 1416–1426Google ScholarPubMed
Chen, W.-Q., Gardner, D. E. & Webb, D. T.. 1996. Biology and life cycle of Atelocauda koae, an unusual demicyclic rust. Mycoscience 37: 91–98CrossRefGoogle Scholar
Clark, D. A. & Clark, D.. 1984. Spacing dynamics of a tropical rain forest tree: evaluation of the Janzen–Connell model. American Naturalist 124: 769–788CrossRefGoogle Scholar
Clark, D. B. & Clark, D. A.. 1985. Seedling dynamics of a tropical tree: impacts of herbivory and meristem damage. Ecology 66: 1884–1892CrossRefGoogle Scholar
Clay, K. 1995. Correlates of pathogen species richness in the grass family. Canadian Journal of Botany 73: S42–S49CrossRefGoogle Scholar
Connell, J. H. 1971. On the role of natural enemies in preventing competitive exclusion in some marine animals and in rain forest trees. In , P. J. Boer & , G. R. Graadwell, eds., Dynamics of Numbers in Populations (Proceedings of the Advanced Study Institute, Osterbeek 1970). Wageningen: Centre for Agricultural Publication and Documentation, pp. 298–312Google Scholar
Dalling, J. W., Swaine, M. D. & Garwood, N. C.. 1998. Dispersal patterns and seed bank dynamics of pioneer trees in moist tropical forest. Ecology 79: 564–578CrossRefGoogle Scholar
Davelos, A. L., Alexander, H. M. & Slade, N. A.. 1996. Ecological genetic interactions between a clonal host plant (Spartina pectinata) and associated rust fungi (Puccinia seymouriana and Puccinia sparganioides). Oecologia 105: 205–213CrossRefGoogle Scholar
Davidson, J. M. 2000. Pathogen-mediated maintenance of diversity and fitness consequences of near versus far pollination for tropical trees. Unpublished Ph.D. dissertation, University of California, Davis
Esquivel, R. E. & Carranza, J.. 1996. Pathogenicity of Phylloporia chrysita (Aphyllophorales: Hymenochaetaceae) on Erythrochiton gymnanthus (Rutaceae). Revista de Biologia Tropical 44: 137–145Google Scholar
Fail, G. L. & Langenheim, J. H.. 1990. Infection processes of Pestalotia subcuticularis on leaves of Hymenaea courbaril. Phytopathology 80: 1259–1265CrossRefGoogle Scholar
Ferrer, A. & Gilbert, G. S.. 2003. Effect of tree host species on fungal community composition in a tropical rain forest in Panama. Diversity and Distributions 9: 455–468CrossRefGoogle Scholar
Fox, L. R. & Morrow, P. A.. 1981. Specialization: species property or local phenomenon?Science 211: 887–893CrossRefGoogle ScholarPubMed
García-Guzmán, G., Burdon, J. J., Ash, J. E. & Cunningham, R. B.. 1996. Regional and local patterns in the spatial distribution of the flower-infecting smut fungus Sporisorium amphilophis in natural populations of its host Bothriochloa macra. New Phytologist 132: 459–469CrossRefGoogle ScholarPubMed
García-Guzmán, G. & Dirzo, R.. 2001. Patterns of leaf-pathogen infection in the understorey of a Mexican rain forest: incidence, spatiotemporal variation, and mechanisms of infection. American Journal of Botany 88: 634–645CrossRefGoogle Scholar
Gardner, D. E. 1994. The native rust fungi of Hawaii. Canadian Journal of Botany 72: 976–989CrossRefGoogle Scholar
Gause, G. F. W. 1934. The Struggle for Existence. Baltimore: Williams and Wilkins
Gilbert, G. S. 1995. Rain forest plant diseases: the canopy-understorey connection. Selbyana 16: 75–77Google Scholar
Gilbert, G. S. 2002. Evolutionary ecology of plant diseases in natural ecosystems. Annual Review of Phytopathology 40: 13–43CrossRefGoogle ScholarPubMed
Gilbert, G. S. & Steven, D.. 1996. A canker disease of seedlings and saplings of Tetragastris panamensis (Burseraceae) caused by Botryosphaeria dothidea in a lowland tropical forest. Plant Disease 80: 684–687CrossRefGoogle Scholar
Gilbert, G. S., Ferrer, A. & Carranza, J.. 2002. Polypore fungal diversity and host density in a moist tropical forest. Biodiversity and Conservation 11: 947–957CrossRefGoogle Scholar
Gilbert, G. S., Hubbell, S. P. & Foster, R. B.. 1994. Density and distance-to-adult effects of a canker disease of trees in a moist tropical forest. Oecologia 98: 100–108CrossRefGoogle Scholar
Gilbert, G. S., Mejía-Chang, M. & Rojas, E.. 2001. Fungal diversity and plant disease in mangrove forests: salt excretion as a possible defense mechanism. Oecologia 132: 278–285CrossRefGoogle Scholar
Gilbert, G. S. & Sousa, W. P.. 2002. Host specialization among wood-decay polypore fungi in a Caribbean mangrove forest. Biotropica 34: 396–404CrossRefGoogle Scholar
Gillett, J. B. 1962. Pest pressure, an underestimated factor in evolution. Systematics Association Publication Number 4: 37–46Google Scholar
Givnish, T. J. 1999. On the causes of gradients in tropical tree diversity. Journal of Ecology 87: 193–210CrossRefGoogle Scholar
Hansen, E. M. & Goheen, E. M.. 2000. Phellinus weirii and other native root pathogens as determinants of forest structure and process in western North America. Annual Review of Phytopathology 38: 515–539CrossRefGoogle ScholarPubMed
Harms, K. E., Wright, S. J., Calderon, O., Hernandez, A. & Herre, E. A.. 2000. Pervasive density-dependent recruitment enhances seedling diversity in a tropical forest. Nature 404: 493–495CrossRefGoogle Scholar
Hawksworth, D. L. 2001. The magnitude of fungal diversity: the 1.5 million species estimate revisited. Mycological Research 105: 1422–1432CrossRefGoogle Scholar
Hille Ris Lambers, J., Clark, J. S. & Beckage, B.. 2002. Density-dependent mortality and the latitudinal gradient in species diversity. Nature 417: 732–735CrossRefGoogle Scholar
Hubbell, S. P. 1997. A unified theory of biogeography and relative species abundance and its application to tropical rain forests and coral reefs. Coral Reefs 16: S9–S21CrossRefGoogle Scholar
Hubbell, S. P. 2001. The Unified Neutral Theory of Biodiversity and Biogeography. Princeton, NJ: Princeton University PressGoogle Scholar
Huhndorf, S. M. & Lodge, D. J.. 1997. Host specificity among wood-inhabiting pyrenomycetes (Fungi, Ascomycetes) in a wet tropical forest in Puerto Rico. Tropical Ecology 38: 307–315Google Scholar
Infante, L. A. 1999. Complex interactions: exploring the role of soilborne plant pathogens in tropical seedling communities. Unpublished M.Sc. thesis, University of California, Berkeley
Janzen, D. H. 1970. Herbivores and the number of tree species in tropical forests. The American Naturalist 104: 501–527CrossRefGoogle Scholar
Kitajima, K. & Augspurger, C. K.. 1989. Seed and seedling ecology of a monocarpic tropical tree, Tachigalia versicolor. Ecology 70: 1102–1114CrossRefGoogle Scholar
Laessøe, T. & Lodge, D. J.. 1994. Three host-specific Xylaria species. Mycologia 86: 436–446CrossRefGoogle Scholar
Langenheim, J. H. & Stubblebine, W. H.. 1983. Variation in leaf resin composition between parent tree and progeny in Hymenaea: implications for herbivory in the humid tropics. Biochemistry Systematics and Ecology 11: 97–106CrossRefGoogle Scholar
Leben, C. 1965. Epiphytic microorganisms in relation to plant disease. Annual Review of Phytopathology 3: 209–230CrossRefGoogle Scholar
Lee, S. S. 1999. Forest health in plantation forests in south-east Asia. Australasian Plant Pathology 28: 283–291Google Scholar
Lindblad, I. 2000. Host specificity of some wood-inhabiting fungi in a tropical forest. Mycologia 92: 399–405CrossRefGoogle Scholar
>Lindblad, I. 2001. Diversity of poroid and some corticoid wood-inhabiting fungi along the rainfall gradient in tropical forests, Costa Rica. Journal of Tropical Ecology 17: 353–369CrossRefGoogle Scholar
Lodge, D. J. 1997. Factors related to diversity of decomposer fungi in tropical forests. Biodiversity and Conservation 6: 681–688CrossRefGoogle Scholar
Lodge, D. J. & Cantrell, S.. 1995. Fungal communities in wet tropical forests: variation in time and space. Canadian Journal of Botany 73: S1391–S1398CrossRefGoogle Scholar
Lodge, D. J., Fisher, P. J. & Sutton, B. C.. 1996. Endophytic fungi of Manilkara bidentata leaves in Puerto Rico. Mycologia 88: 733–738CrossRefGoogle Scholar
May, R. M. 1991. A fondness for fungi. Nature 352: 475–476CrossRefGoogle Scholar
Meza, M. R. 1992. La pudrición del duramen de los Arboles en pie en Venezuela. El caso de la Mora de la Guayana. Unpublished Master's thesis, Universidad de Los Andes
Opoku, I. Y., Akrofi, A. Y. & Appiah, A. A.. 2002. Shade trees are alternative hosts of the cocoa pathogen Phytophthora megakarya. Crop Protection 21: 629–634CrossRefGoogle Scholar
Packer, A. & Clay, K.. 2000. Soil pathogens and spatial patterns of seedling mortality in a temperate tree. Nature 404: 278–281CrossRefGoogle Scholar
Polishook, J. D., Bills, G. F. & Lodge, D. J.. 1996. Microfungi from decaying leaves of two rain forest trees in Puerto Rico. Journal of Industrial Microbiology 17: 284–294CrossRefGoogle Scholar
Putz, F. E., Coley, P. D., Lu, K., Montalvo, A. & Aiello, A.. 1983. Uprooting and snapping of trees: structural determinants and ecological consequences. Canadian Journal of Forest Research 13: 1011–1020CrossRefGoogle Scholar
Richardson, K. A. & Currah, R. S.. 1995. The fungal community associated with the roots of some rainforest epiphytes of Costa Rica. Selbyana 16: 49–73Google Scholar
Rizzo, D. M. & Garbelotto, M.. 2003. Sudden oak death: endangering California and Oregon forest ecosystems. Frontiers in Ecology and the Environment 1: 197–204CrossRefGoogle Scholar
Rodrigues, K. F. 1994. The foliar fungal endophytes of the Amazonian palm Euterpe oleracea. Mycologia 86: 376–385CrossRefGoogle Scholar
Sánchez Garduño, C., S. J. Wright & C. Potvin. 1995. Seed predation. In S. J. Wright & M. Colley, eds., Accessing the Canopy. Panama: United Nations Environment Programme/ Smithsonian Tropical Research Institute, pp. 18–19
Schoeman, M. H., Manicom, B. Q. & Wingfield, M. J.. 1995. Epidemiology of powdery mildew on mango blossoms. Plant Disease 79: 524–528CrossRefGoogle Scholar
Sequiera, L. 1958. The host range of Mycena citricolor (Berk. & Curt.) Sacc. Turrialba 8: 136–147Google Scholar
Stevens, F. L. 1927. Fungi from Costa Rica and Panama. Illinois Biological Monographs 11: 1–255Google Scholar
Suryanarayanan, T. S. & Rajagopal, K.. 2000. Fungal endophytes (Phellophytes) of some tropical forest trees. Indian Forester 126: 165–170Google Scholar
Tilman, D. 1982. Resource Competition and Community Structure. Princeton, NJ: Princeton University PressGoogle ScholarPubMed
Travers, S. E., Gilbert, G. S. & Perry, E. F.. 1998. The effect of rust infection on reproduction in a tropical tree (Faramea occidentalis). Biotropica 30: 438–443CrossRefGoogle Scholar
Putten, W. H. & Peters, B. A. M.. 1997. How soil-borne pathogens may affect plant competition. Ecology 78: 1785–1795CrossRefGoogle Scholar
Vánky, K. 2002. Illustrated Genera of Smut Fungi, 2nd edn. St Paul, MN: APS PressGoogle Scholar
Webb, C. O. & Peart, D. R.. 1999. Seedling density dependence promotes coexistence of Bornean rain forest trees. Ecology 80: 2006–2017CrossRefGoogle Scholar
Wellman, F. L. 1968. More diseases on crops in the tropics than in the temperate zone. Ceiba 14: 17–28Google Scholar
Wellman, F. L. & Echandi, E.. 1981. The coffee rust situation in Latin America in 1980. Phytopathology 71: 968–971CrossRefGoogle Scholar
Weste, G. & Marks, G. C.. 1987. The biology of Phytophthora cinnamomi in Australasian forests. Annual Review of Phytopathology 25: 207–229CrossRefGoogle Scholar
Weston, W. H. 1933. The fungi of Barro Colorado. Science Monthly 36Google Scholar
Wilson, D. 1995. Endophyte – the evolution of a term, and clarification of its use and definition. Oikos 73CrossRefGoogle Scholar
Worrall, J. J. & Harrington, T. C.. 1988. Etiology of canopy gaps in spruce-fir forests at Crawford Notch, New Hampshire [USA]. Canadian Journal of Forest Research 18: 1463–1469CrossRefGoogle Scholar

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