Host specificity of insect herbivores in tropical forests
Jazyk angličtina Země Anglie, Velká Británie Médium print
Typ dokumentu časopisecké články, práce podpořená grantem, Research Support, U.S. Gov't, Non-P.H.S., přehledy
PubMed
16024368
PubMed Central
PMC1559807
DOI
10.1098/rspb.2004.3023
PII: M4JP8BARPW8K3XFF
Knihovny.cz E-zdroje
- MeSH
- demografie MeSH
- ekologie metody MeSH
- ekosystém * MeSH
- fylogeneze MeSH
- hmyz fyziologie MeSH
- potravní řetězec * MeSH
- stravovací zvyklosti fyziologie MeSH
- stromy * MeSH
- tropické klima MeSH
- zvířata MeSH
- Check Tag
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- přehledy MeSH
- Research Support, U.S. Gov't, Non-P.H.S. MeSH
Studies of host specificity in tropical insect herbivores are evolving from a focus on insect distribution data obtained by canopy fogging and other mass collecting methods, to a focus on obtaining data on insect rearing and experimentally verified feeding patterns. We review this transition and identify persisting methodological problems. Replicated quantitative surveys of plant-herbivore food webs, based on sampling efforts of an order of magnitude greater than is customary at present, may be cost-effectively achieved by small research teams supported by local assistants. Survey designs that separate historical and ecological determinants of host specificity by studying herbivores feeding on the same plant species exposed to different environmental or experimental conditions are rare. Further, we advocate the use of host-specificity measures based on plant phylogeny. Existing data suggest that a minority of species in herbivore communities feed on a single plant species when alternative congeneric hosts are available. Thus, host plant range limits tend to coincide with those of plant genera, rather than species or suprageneric taxa. Host specificity among tropical herbivore guilds decreases in the sequence: granivores > leaf-miners > fructivore > leaf-chewers = sap-suckers > xylophages > root-feeders, thus paralleling patterns observed in temperate forests. Differences in host specificity between temperate and tropical forests are difficult to assess since data on tropical herbivores originate from recent field studies, whereas their temperate counterparts derive from regional host species lists, assembled over many years. No major increase in host specificity from temperate to tropical communities is evident. This conclusion, together with the recent downward revisions of extremely high estimates of tropical species richness, suggest that tropical ecosystems may not be as biodiverse as previously thought.
Zobrazit více v PubMed
Barone J.A. Host-specificity of folivorous insects in a moist tropical forest. J. Anim. Ecol. 1998;67:400–409.
Basset Y. Host specificity of arboreal and free-living insect herbivores in rain forests. Biol. J. Linn. Soc. 1992;47:115–133.
Basset Y. Local communities of arboreal herbivores in Papua New Guinea: predictors of insect variables. Ecology. 1996;77:1909–1916.
Basset Y. Invertebrates in the canopy of tropical rain forests—how much do we really know? Plant Ecol. 2001a;153:87–107.
Basset Y. Communities of insect herbivores foraging on saplings versus mature trees of Pourouma bicolor (Cecropiaceae) in Panama. Oecologia. 2001b;129:253–260. PubMed
Basset Y, Charles E. An annotated list of insect herbivores foraging on the seedlings of five forest trees in Guyana. Anais da Sociedade Entomológica do Brasil. 2000;29:433–452.
Basset Y, Novotny V. Species richness of insect herbivore communities on Ficus in Papua New Guinea. Biol. J. Linn. Soc. 1999;67:477–499.
Basset Y, Samuelson G.A, Allison A, Miller S.E. How many species of host-specific insect feed on a species of tropical tree? Biol. J. Linn. Soc. 1996;59:201–216.
Basset Y, Charles E, Hammond D.S, Brown V.K. Short-term effects of canopy openness on insect herbivores in a rain forest in Guyana. J. Appl. Ecol. 2001;38:1045–1058.
Basset Y, Novotny V, Miller S.E, Kitching R, editors. Arthropods of tropical forests: spatio-temporal dynamics and resource use in the canopy. Cambridge University Press; Cambridge, UK: 2003.
Basset Y, Novotny V, Miller S.E, Weiblen G.D, Missa O, Stewart A.J.A. Conservation and biological monitoring of tropical forests: the role of parataxonomists. J. Appl. Ecol. 2004;41:163–174.
Beaver R.A. Host specificity of temperate and tropical animals. Nature. 1979;281:139–141.
Becerra J.X. Insects on plants: macroevolutionary chemical trends in host use. Science. 1997;276:253–256. PubMed
Berkov A. The impact of redefined species limits in Palame (Coleoptera: Cerambycidae: Lamiinae: Acanthocinini) on assessments of host, seasonal, and stratum specificity. Biol. J. Linn. Soc. 2002;76:195–209.
Berkov A, Tavakilian G. Host utilization of the Brazil nut family (Lecythidaceae) by sympatric wood-boring species of Palame (Coleoptera, Cerambycidae, Lamiinae, Acanthocinini) Biol. J. Linn. Soc. 1999;67:181–198.
Brown V.K, Southwood T.R.E. Trophic diversity, niche breadth and generation times of exopterygote insects in a secondary succession. Oecologia. 1983;56:220–225. PubMed
Brehm G, Sussenbach D, Fiedler K. Unique elevational diversity patterns of geometrid moths in an Andean montane rainforest. Ecography. 2003;26:456–466.
Coley P.D. Herbivory and defensive characteristics of tree species in a lowland tropical forest. Ecol. Monogr. 1983;53:209–233.
Coley P.D, Barone J.A. Herbivory and plant defenses in tropical forests. Annu. Rev. Ecol. Syst. 1996;27:305–335.
Condit R, Hubbell S.P, Foster R.B. Changes in tree species abundance in a neotropical forest: impact of climate change. J. Trop. Ecol. 1996;12:231–256.
Diniz I.R, Morais H.C. Lepidoptera caterpillar fauna of cerrado host plants. Biodivers. Conserv. 1997;6:817–836.
Dyer L.A. Tasty generalists and nasty specialists—antipredator mechanisms in tropical lepidopteran larvae. Ecology. 1995;76:1483–1496.
Dyer L.A, Palmer A.D.N, editors. Piper: a model genus for studies of phytochemistry, ecology, and evolution. Kluwer Academic/Plenum Publishers; New York: 2004.
Erwin T.L. Tropical forests: their richness in Coleoptera and other arthropod species. Coleopt. Bull. 1982;36:74–75.
Fiedler K. Lycaenid butterflies and plants: host–plant relationships, tropical versus temperate. Ecotopica. 1995;1:51–58.
Fiedler K. Diet breadth and host plant diversity of tropical- vs. temperate-zone herbivores: south-east Asian and west Palaearctic butterflies as a case study. Ecol. Entomol. 1998;23:285–297.
Flowers R.W, Janzen D.H. Feeding records of Costa Rican leaf beetles (Coleoptera: Chrysomelidae) Florida Entomol. 1997;80:334–366.
Frenzel M, Brandl R. Hosts as habitats: faunal similarity of phytophagous insects between host plants. Ecol. Entomol. 2001;26:594–601.
Futuyma D.J, Gould F. Associations of plants and insects in a deciduous forest. Ecol. Monogr. 1979;49:33–50.
Gentry G.L, Dyer L.A. On the conditional nature of neotropical caterpillar defenses against their natural enemies. Ecology. 2002;83:3108–3119.
Godfray H.C.J, Lewis O.T, Memmott J. Studying insect diversity in the tropics. Phil. Trans. R. Soc. B. 1999;354:1811–1824. PubMed PMC
Hebert P.D.N, Ratsingham S, Dewaard J.R. Barcoding animal life: cytochrome c oxidase subunit 1 divergences among closely related species. Proc. R. Soc. B. 2003;270(Suppl.):S96–S99. PubMed PMC
Hopkins M.J.G. Unusual diversities of seed beetles (Coleoptera: Bruchidae) on Parkia (Leguminosae: Mimosoideae) in Brazil. Biol. J. Linn. Soc. 1983;19:329–338.
Hurlbert S.H. The nonconcept of species diversity: a critique and alternative parameters. Ecology. 1971;52:577–586. PubMed
Janzen D.H. Specificity of seed-attacking beetles in a Costa Rican deciduous forest. J. Ecol. 1980;68:929–952.
Janzen D.H. Food webs: who eats what, why, how, and with what effects in a tropical forest? In: Golley F.B.I, editor. Tropical rain forest ecosystems. Elsevier; Amsterdam: 1983. pp. 167–182.
Janzen D.H. How polyphagous are Costa Rican dry forest saturniid caterpillars? In: Basset Y, Novotny V, Miller S.E, Kitching R, editors. Arthropods of tropical forests: spatio-temporal dynamics and resource use in the canopy. Cambridge University Press; Cambridge, UK: 2003. pp. 369–379.
Janzen, D. H. & Hallwachs, W. 2004 Caterpillar rearing voucher databases for the Area de Conservación in northwestern Costa Rica. Published at http://janzen.sas.upenn.edu/caterpillars/database.htm
Kelly C.K, Southwood T.R.E. Species richness and resource availability: a phylogenetic analysis on insects associated with trees. Proc. Natl Acad. Sci. USA. 1999;96:8013–8016. PubMed PMC
Kursar T.A, Coley P.D. Convergence in defense syndromes of young leaves in tropical rainforests. Biochem. Syst. Ecol. 2003;31:929–949.
LaFrankie J.V. The contribution of large-scale forest dynamic plots to theoretical community ecology. In: Turner I.M, Diong C.H, Lim S.S.L, Ng P.K.L, editors. Biodiversity and the dynamics of ecosystems, vol. 1. National University of Singapore; Singapore: 1996. pp. 63–79.
Lawton J.H, Lewinsohn T.M, Compton S.G. Patterns of diversity for insect herbivores on bracken. In: Ricklefs R.E, Schluter D, editors. Species diversity in ecological communities. Historical and geographical perspectives. University of Chicago Press; Chicago, IL: 1993. pp. 178–184.
Leps J, Novotny V, Basset Y. Effect of habitat and successional optimum of host plants on the composition of their herbivorous communities: leaf-chewing insects on shrubs and trees in New Guinea. J. Ecol. 2001;89:186–199.
Lewinsohn T.M. Insects in flower heads of Asteraceae in southeast Brazil: a case study on tropical species richness. In: Price P.W, Lewinsohn T.M, Fernandes G.W, Benson W.W, editors. Plant–animal interactions: evolutionary ecology in tropical and temperate regions. Wiley; New York: 1991. pp. 525–559.
Lewis O.T, Memmott J, Lasalle J, Lyal C.H.C, Whitefoord C, Godfray H.C.J. Structure of a diverse tropical forest insect–parasitoid community. J. Anim. Ecol. 2002;71:855–873.
Loye J.E. Ecological diversity and host plant relationships of treehoppers in a lowland tropical rainforest (Homoptera: Membracidae and Nicomiidae) In: Quintero D, Aiello A, editors. Insects of Panama and MesoAmerica. Oxford University Press; Oxford, UK: 1992. pp. 280–289.
Marquis R.J. Herbivore fauna of Piper (Piperaceae) in a Costa Rican wet forest: diversity, specificity and impact. In: Price P.W, Lewinsohn T.M, Fernandes G.W, Benson W.W, editors. Plant–animal interactions: evolutionary ecology in tropical and temperate regions. Wiley; New York: 1991. pp. 179–208.
Mattson W.J, Lawrence R.K, Haack R.A, Herms D.A, Charles P.-J. Defensive strategies of woody plants against different insect-feeding guilds in relation to plant ecological strategies and intimacy of association with insects. In: Mattson W.J, Levieux J, Bernard-Dagan C, editors. Mechanisms of woody plant defenses against insects: search for pattern. New York: Springer; 1988. pp. 1–38.
Morris R.J, Lewis O.T, Godfray H.C.J. Experimental evidence for apparent competition in a tropical forest web. Nature. 2004;428:310–313. PubMed
Müller C.B, Adriaanse I.C.T, Belshaw R, Godfray H.C.J. The structure of an aphid–parasitoid community. J. Anim. Ecol. 1999;68:346–370.
Nakagawa M, et al. Resource use of insect seed predators during general flowering and seeding events in a Bornean dipterocarp rain forest. Bull. Entomol. Res. 2003;93:455–466. PubMed
Novotny V, Basset Y. Seasonality of sap-sucking insects (Auchenorrhyncha, Hemiptera) feeding on Ficus (Moraceae) in a lowland rain forest in New Guinea. Oecologia. 1998;115:514–522. PubMed
Novotny V, Basset Y, Miller S.E, Drozd P, Cizek L. Host specialisation of leaf chewing insects in a New Guinea rainforest. J. Anim. Ecol. 2002;71:400–412.
Novotny V, Basset Y, Miller S.E, Weiblen G.D, Bremer B, Cizek L, Drozd P. Low host specificity of herbivorous insects in a tropical forest. Nature. 2002;416:841–844. PubMed
Novotny V, Miller S.E, Basset Y, Cizek L, Drozd P, Darrow K, Leps J. Predictably simple: communities of caterpillars (Lepidoptera) feeding on rainforest trees in Papua New Guinea. Proc. R. Soc. B. 2002;269:2337–2344. PubMed PMC
Novotny V, Basset Y, Miller S.E, Kitching R, Laidlaw M, Drozd P, Cizek L. How many insect species feed on woody plants from one hectare of a lowland rainforest? Conserv. Biol. 2004;18:227–237.
Novotny V, Miller S.E, Basset Y, Cizek L, Kaupa B, Kua J, Weiblen G.D. An altitudinal comparison of caterpillar (Lepidoptera) assemblages on Ficus trees in Papua New Guinea. J. Biogeogr. In press
Novotny V, Miller S.E, Leps J, Bito D, Janda M, Hulcr J, Basset Y, Damas K, Weiblen G.D. No tree an island: the plant–caterpillar food web of secondary rainforest in New Guinea. Ecol. Lett. 2004;7:1090–1100.
Novotny V, Clarke A.T, Drew R.A.I, Balagawi S, Clifford B. Host specialization and species richness of fruit flies (Diptera: Tephritidae) in a New Guinea rainforest. J. Trop. Ecol. 2005;21:67–77.
Ødegaard F. The relative importance of trees versus lianas as hosts for phytophagous beetles (Coleoptera) in tropical forests. J. Biogeogr. 2000a;27:283–296.
Ødegaard F. How many species of arthropods? Ervin's estimate revised. Biol. J. Linn. Soc. 2000b;71:583–597.
Ødegaard F. Species richness of phytophagous beetles in the tropical tree Brosimum utile (Moraceae): the effects of sampling strategy and the problem of tourists. Ecol. Entomol. 2004;29:76–88.
Ollerton J, Cranmer L. Latitudinal trends in plant–pollinator interactions: are tropical plants more specialised? Oikos. 2002;98:340–350.
Pokon R, Novotny V, Samuelson G.A. Host specialization and species richness of root feeding chrysomelid larvae (Chrysomelidae, Coleoptera) in a New Guinea rainforest. J. Trop. Ecol. In press
Price P.W. Resource-driven terrestrial interaction webs. Ecol. Res. 2002;17:241–247.
Rowell H.F. Food plant specificity in neotropical rain-forest acridids. Entomol. Exp. Appl. 1978;24:651–662.
Scoble M.J, Gaston K.J, Crook A. Using taxonomic data to estimate species richness in Geometridae. J. Lep. Soc. 1995;49:136–147.
Scriber J.M. Tale of the tiger: Beringial biogeography, binomial classification, and breakfast choices in the Papilio glaucus complex of butterflies. In: Spencer K.C, editor. Chemical mediation of coevolution. Academic Press; New York: 1988. pp. 241–301.
Shanahan M, Harrison R.D, Yamuna R, Bowen W, Thornton I.W.B. Colonization of an island volcano, Long Island, Papua New Guinea, and an emergent island, Motmot, in its caldera lake. V. Colonization by figs (Ficus spp.), their dispersers and pollinators. J. Biogeogr. 2001;28:1365–1377.
Stork N.E, Adis J, Didham R.K, editors. Canopy arthropods. Chapman & Hall; London: 1997.
Symons F.B, Beccaloni G.W. Phylogenetic indices for measuring the diet breadths of phytophagous insects. Oecologia. 1999;119:427–434. PubMed
Tavakilian G, Berkov A, Meurer-Grimes B, Mori S. Neotropical tree species and their faunas of xylophagous longicorns (Coleoptera: Cerambycidae) in French Guiana. Bot. Rev. 1997;63:303–355.
Thomas C.D. Herbivore diets, herbivore colonization, and the escape hypothesis. Ecology. 1990;71:610–615.
Ward L.K. The validity and interpretation of insect foodplant records. Br. J. Entomol. Nat. Hist. 1988;1:153–161.
Ward L.K, Hackshaw A, Clarke R.T. Food-plant families of British insects and mites: the influence of life form and plant family. Biol. J. Linn. Soc. 1995;55:109–127.
Webb C.O. Exploring the phylogenetic structure of ecological communities: an example for rain forest trees. Am. Nat. 2000;156:145–155. PubMed
Webb C.O, Ackerly D.D, McPeek M.A, Donoghue M.J. Phylogenies and community ecology. Annu. Rev. Ecol. Syst. 2002;33:475–505.
Weiblen G.D. Correlated evolution in fig pollination. Syst. Biol. 2004;53:1–12. PubMed
Weiblen G.D, Webb C.O, Novotny V, Basset Y, Miller S.E. Phylogenetic dispersion of host use in a tropical insect herbivore community. Ecology. In press PubMed
Wood T.K. Life history patterns of tropical membracids (Homoptera: Membracidae) Sociobiology. 1984;8:299–344.
Wright S.J. Plant diversity in tropical forests: a review of mechanisms of species coexistence. Oecologia. 2002;130:1–14. PubMed
Climate, host and geography shape insect and fungal communities of trees
Quantitative assessment of plant-arthropod interactions in forest canopies: A plot-based approach
Variably hungry caterpillars: predictive models and foliar chemistry suggest how to eat a rainforest