Skip to main content

Moths at tropical forest margins — how mega-diverse insect assemblages respond to forest disturbance and recovery

  • Chapter
Stability of Tropical Rainforest Margins

Part of the book series: Environmental Science and Engineering ((ENVSCIENCE))

Abstract

Tropical forest moth ensembles are often extraordinarily rich in species and complex in structure. There is an increasing number of quantitative studies from all major tropical realms which now allows for a more rigorous assessment of the ways how such ensembles change along habitat transects from the natural forest towards the edge of large conservation areas, or in the course of forest recovery at such margins. Such knowledge is also essential for deciding if moths can be used for monitoring the biotic effects of forest disturbance on mega-diverse insect faunas at all, and which moth groups are the most suitable targets for this purpose. Using very large data sets from low (Mt. Kinabalu National Park, Borneo) and high elevations (Podocarpus National Park, Ecuador), we investigate how species richness and species composition of moths change at small spatial scales along gradients of disturbance at the edge of natural forest reserves. Local species diversity did not always decline, and sometimes even increased, along the gradients. Ensembles of moths from the families Arctiidae or Sphingidae were as rich as in natural forest, or were even more diverse in habitats close to the forest margin. Geometridae and Pyraloidea ensembles, in contrast, tended to be impoverished. Correlations of alpha diversity measures between moth taxa were often poor and thus did not allow for using one group as a ‘biodiversity indicator’ of others. Estimates of local diversity also depended on the temporal scale of assessment. Species composition was remarkably sensitive to habitat alterations at forest edges even at very small spatial scales, despite the high dispersal potential of many moths. Patterns of beta diversity were highly concordant across unrelated moth taxa with very different life history syndromes. Geometridae ensembles responded more sensitively to changes in canopy openness than arctiid moths and yielded more robust results with regard to sampling effects. Therefore geometrids are particularly promising candidates for environmental monitoring in tropical landscapes. Much of the faunal differentiation between forest and margin habitats was due to shifts in abundance relationships, and not to the presence or absence of ‘indicator species’. Therefore, abundance-based monitoring appears more appropriate to detect effects of environmental change on mega-diverse moth ensembles. Our results suggest that patterns of beta (rather than alpha) diversity are generally more meaningful to assess the impact of processes at forest edges relevant to nature conservation and landscape planning.

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Chapter
USD 29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 169.00
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD 219.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info
Hardcover Book
USD 219.99
Price excludes VAT (USA)
  • Durable hardcover edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

References

  • Armenteras D, Gast F, Villareal H (2003) Andean forest fragmentation and the representativeness of protected natural areas in the eastern Andes, Colombia. Biol Conserv 113: 245–256

    Article  Google Scholar 

  • Axmacher JC, Fiedler K (2004) Manual versus automatic moth sampling at equal light sources — a comparison of catches from Mt. Kilimanjaro. J Lepid Soc 58: 196–202

    Google Scholar 

  • Axmacher JC, Tünte H, Schrumpf M, Müller-Hohenstein K, Lyaruu HVM, Fiedler K (2004) Diverging diversity patterns of vascular plants and geometrid moths during forest regeneration on Mt. Kilimanjaro, Tanzania. J Biogeogr 31: 895–904

    Article  Google Scholar 

  • Basset Y, Charles E, Hammond DS, Brown VK (2001) Short-term effects of canopy openness on insect herbivores in a rain forest in Guyana. J Appl Ecol 38: 1045–1058

    Article  Google Scholar 

  • Beck J, Kitching IJ, Linsenmair KE (2006) Effects of habitat disturbance can be subtle yet significant: biodiversity of hawkmoth assemblages (Lepidoptera: Sphingidae) in Southeast-Asia. Biodiv Conserv 15: 465–486

    Article  Google Scholar 

  • Beck J, Linsenmair KE (2006) Feasibility of light-trapping in community research on moths: attraction radius of light, completeness of samples, nightly flight times and seasonality of Southeast-Asian hawkmoths (Lepidoptera: Sphingidae). J Res Lepid 39 (in press)

    Google Scholar 

  • Beck J, Schulze CH, Linsenmair KE, Fiedler K (2002) From forest to farmland: diversity of geometrid moths along two habitat gradients on Borneo. J Trop Ecol 18: 33–51

    Article  Google Scholar 

  • Benjamini Y, Hochberg Y (1995) Controlling the false discovery rate: a practical and powerful approach to multiple testing. J R Statist Soc B57: 289–300

    Google Scholar 

  • Brehm G, Fiedler K (2003) Faunal composition of geometrid moths changes with altitude in an Andean montane rain forest. J Biogeogr 30: 431–440

    Article  Google Scholar 

  • Brehm G, Fiedler K (2004) Ordinating tropical moth ensembles from an elevational gradient: a comparison of common methods. J Trop Ecol 20: 165–172

    Article  Google Scholar 

  • Brehm G, Fiedler K (2005) Diversity and community structure of geometrid moths of disturbed habitat in a montane area in the Ecuadorian Andes. J Res Lepid 38: 1–14

    Google Scholar 

  • Brehm G, Homeier J, Fiedler K (2003) Beta diversity of geometrid moths (Lepidoptera: Geometridae) in an Andean montane rainforest. Diversity Distrib 9: 351–366

    Article  Google Scholar 

  • Brehm G, Pitkin LM, Hilt N, Fiedler K (2005) Montane Andean rain forests are a global diversity hotspot of geometrid moths. J Biogeogr 32: 1621–1627

    Article  Google Scholar 

  • Brooks TM, Mittermeier RA, Mittermeier CG, da Fonseca GAB, Rylands AB, Konstant WR, Flick P, Pilgrim J, Oldfield S, Magin G, Hilton-Taylor C (2002) Habitat loss and extinction in the hotspots of biodiversity. Conserv Biol 16: 909–923

    Article  Google Scholar 

  • Camargo JLC, Kapos V (1995) Complex edge effects on soil moisture and microclimate in central Amazonian forest. J Trop Ecol 11: 205–221

    Google Scholar 

  • Chey VK, Holloway JD, Speight MR (1997) Diversity of moths in forest plantations and natural forests in Sabah. Bull Entomol Res 87: 371–385

    Article  Google Scholar 

  • Clarke KR (1993) Non-parametric multivariate analyses of changes in community structure. Austral J Ecol 18: 117–143

    Article  Google Scholar 

  • Clarke KR, Gorley RN (2001) PIMER v5: user manual/tutorial. Primer-E, Plymouth

    Google Scholar 

  • Davies-Colley RJ, Payne GW, van Elswijk M (2000) Microclimate gradients across a forest edge. New Zealand J Ecol 24: 111–121

    Google Scholar 

  • Fauth JE, Bernardo J, Camara M, Resetarits WJ, van Buskirk J, McCollum SA (1996) Simplifying the jargon of community ecology: a conceptual approach. Am Nat 147: 282–286

    Article  Google Scholar 

  • Fiedler K, Schulze CH (2004) Forest modification affects diversity (but not dynamics) of speciose tropical pyraloid moth communities. Biotropica 36: 615–627

    Google Scholar 

  • Fox BJ, Taylor JE, Fox MD, Williams C (1997) Vegetation changes across edges of rainforest remnants. Biol Conserv 82: 1–13

    Article  Google Scholar 

  • Gotelli NJ, Colwell RK (2001) Quantifying biodiversity: procedures and pitfalls in the measurement and comparison of species richness. Ecol Letts 4: 379–391

    Article  Google Scholar 

  • Hamer KC, Hill JK (2000) Scale-dependent effects of habitat disturbance on species richness in tropical forests. Conserv Biol 14: 1435–1440

    Article  Google Scholar 

  • Hill JK, Hamer KC (2004) Determining impacts of habitat modification on diversity of tropical forest fauna: the importance of spatial scale. J Appl Ecol 41: 744–754

    Article  Google Scholar 

  • Hilt N (2005) Diversity and species composition of two different moth families (Lepidoptera: Arctiidae vs. Geometridae) along a successional gradient in the Ecuadorian Andes. PhD thesis, Univ Bayreuth. URL: http://opus.ub.uni-bayreuth.de/volltexte/2006/201

    Google Scholar 

  • Hilt N, Fiedler K (2005) Diversity and composition of Arctiidae moth ensembles along a successional gradient in the Ecuadorian Andes. Diversity Distrib 11: 387–398

    Article  Google Scholar 

  • Hilt N, Fiedler K (2006) Arctiid moth ensembles along a successional gradient in the Ecuadorian montane rain forest zone: how different are subfamilies and tribes? J Biogeogr 33: 108–120

    Article  Google Scholar 

  • Hilt N, Brehm G, Fiedler K (2006) Diversity and ensemble composition of geometrid moths along a successional gradient in the Ecuadorian Andes. J Trop Ecol 22: 155–166

    Article  Google Scholar 

  • Holloway JD (1985) Moths as indicator organisms for categorising rain forest and monitoring changes and regenerating processes. In: Chadwick AC, Sutton SL (eds) Tropical rain forest: the Leeds symposium. Philosophical and Literary Society, Leeds, pp 235–242

    Google Scholar 

  • Holloway JD (1998) The impact of traditional and modern cultivation practices, including forestry, on lepidopteran diversity in Malaysia and Indonesia. In: Newbery DM, Prins HHT, Brown ND (eds) Dynamics of tropical ecosystems. Blackwell, Oxford, pp 567–597

    Google Scholar 

  • Holloway JD, Kirk-Spriggs AH, Chey VK (1992) The response of some rain forest insect groups to logging and conversion to plantation. Phil Trans R Soc Lond B 335: 425–436

    Article  Google Scholar 

  • Holloway JD, Kibby G, Peggie D (2001) The families of Malesian moths and butterflies. Brill, Leiden

    Google Scholar 

  • Homeier J (2004) Baumdiversität, Waldstruktur und Wachstumsdynamik zweier tropischer Bergregenwälder in Ecuador und Costa Rica. Diss Bot 391: 1–207

    Google Scholar 

  • Intachat J, Holloway JD, Speight MR (1997) The effect of different forest management practices on geometroid moth populations and their diversity in Peninsular Malaysia. J Trop Forest Sci 9: 411–430

    Google Scholar 

  • Intachat J, Holloway JD, Speight MR (1999) The impact of logging on geometroid moth populations and their diversity in lowland forests of Peninsular Malaysia. J Trop Forest Sci 11: 61–78

    Google Scholar 

  • Jacobson NL, Weller SJ (2002) A cladistic study of the Arctiidae (Lepidoptera) by using characters of immatures and adults. Thomas Say Publications in Entomology: Monographs. Entomological Society of America, Lanham

    Google Scholar 

  • Kitching RL, Orr AG, Thalib L, Mitchell H, Hopkins MS, Graham AW (2000) Moth assemblages as indicators of environmental quality in remnants of upland Australian rain forest. J Appl Ecol 37: 284–297

    Article  Google Scholar 

  • Kitching IJ, Rawlins JE (1999) The Noctuoidea. In: Kristensen NP (ed) Handbook of zoology, vol 1, part 1, Lepidoptera, moths and butterflies. De Gruyter, Berlin, New York, pp 355–401

    Google Scholar 

  • Krell F-T (2004) Parataxonomy vs. taxonomy in biodiversity studies — pitfalls and applicability of ‘morphospecies’ sorting. Biodiv Conserv 13: 795–812

    Article  Google Scholar 

  • Kristensen NP (1999) Lepidoptera, moths and butterflies. In: Fischer M (ed) Handbook of zoology, vol 1, part 1. De Gruyter, Berlin, New York

    Google Scholar 

  • Laurance WF (1998) A crisis in the making: responses of Amazonian forests to land use and climate change. Trends Ecol Evol 13: 411–415

    Article  Google Scholar 

  • Laurance WF, Lovejoy TE, Vasconcelos HL, Bruna EM, Didham RK, Stouffer PC, Gascon C, Bierregaard RO, Laurance SG, Sampaio E (2002) Ecosystem decay of Amazonian forest fragments: a 22-year investigation. Conserv Biol 16: 605–618

    Article  Google Scholar 

  • Lawton JH, Bignell DE, Bolton B, Bloemers GF, Eggleton P, Hammond PM, Hodda M, Holt RD, Larsen TB, Mawdsley NA, Stork NE, Srivastava DS, Watt AD (1998) Biodiversity inventories, indicator taxa and effects of habitat modification in tropical forest. Nature 391: 72–75

    Article  CAS  Google Scholar 

  • Legendre P, Legendre L (1998) Numerical ecology, 2nd ed. Elsevier, Amsterdam

    Google Scholar 

  • Lepš J, Novotný V, Basset Y (2001) Habitat and successional status of plants in relation to the communities of their leaf-chewing herbivores in Papua New Guinea. J Ecol 89: 186–199

    Article  Google Scholar 

  • Madsen JE, Øllgaard B (1994) Floristic composition, structure, and dynamics of an upper montane rain forest in Southern Ecuador. Nordic J Bot 14: 403–423

    Article  Google Scholar 

  • Meijaard E, Sheil D, Nasi R, Augeri D, Rosenbaum B, Iskandar D, Setyawati T, Lammertink M, Rachmatika I, Wong A, Soehartono T, Stanley S, O’Brien T (2005) Life after logging: reconciling wildlife conservation and production forestry in Indonesian Borneo. Center for International Forestry Research, Bogor

    Google Scholar 

  • Mesquita RCG, Delamônica P, Laurance WF (1999) Effect of surrounding vegetation on edge-related tree mortality in Amazonian forest fragments. Biol Conserv 91: 129–134

    Article  Google Scholar 

  • Muirhead-Thomson RC (1991) Trap responses of flying insects. Academic Press, London

    Google Scholar 

  • Murcia C (1995) Edge effects in fragmented forests: implications for conservation. Trends Ecol Evol 10: 58–62

    Article  Google Scholar 

  • Myers N, Mittermeier RA, Mittermeier CG, da Fonseca GAB, Kent J (2000) Biodiversity hotspots for conservation priorities. Nature 403: 853–858

    Article  CAS  Google Scholar 

  • Newmark WD (2001) Tanzanian forest edge microclimatic gradients: dynamic patterns. Biotropica 33: 2–11

    Google Scholar 

  • Novotný V, Basset Y (2000) Rare species in communities of tropical insect herbivores: pondering the mystery of singletons. Oikos 89: 564–572

    Article  Google Scholar 

  • Økland RH (1996) Are ordination and constrained ordination alternative or complementary strategies in general ecological studies? J Veget Sci 7: 289–292

    Article  Google Scholar 

  • Paulsch A (2002) Development and application of a classification system for undisturbed and disturbed tropical montane forest based on vegetation structure. PhD thesis, Univ Bayreuth. URL: http://opus.ub.unibayreuth.de/volltexte/2002/1

    Google Scholar 

  • Rahbek C (2005) The role of spatial scale and the perception of large-scale species-richness patterns. Ecol Letts 8: 224–239

    Article  Google Scholar 

  • Ricketts TH, Daily GC, Ehrlich PR, Fay JP (2001) Countryside biogeography of moths in a fragmented landscape: biodiversity in native and agricultural habitats. Conserv Biol 15: 378–388

    Article  Google Scholar 

  • Rosenzweig ML (1995) Species diversity in space and time. Cambridge Univ Press, Cambridge

    Google Scholar 

  • Sattler K (1991) A review of wing reduction in Lepidoptera. Bull Br Mus Nat Hist (Ent) 60: 243–288

    Google Scholar 

  • Sayer J, Ishwaran N, Thorsell J, Sigaty T (2000) Tropical forest biodiversity and the World Heritage Convention. Ambio 29: 302–309

    Article  Google Scholar 

  • Schulze CH (2000) Auswirkungen anthropogener Störungen auf die Diversität von Herbivoren — Analysen von Nachtfalterzönosen entlang von Habitat-gradienten in Ost-Malaysia. PhD thesis, Univ Bayreuth

    Google Scholar 

  • Schulze CH, Fiedler K (2003) Hawkmoth diversity in northern Borneo does not reflect the influence of anthropogenic habitat disturbance. Ecotropica 9: 99–102

    Google Scholar 

  • Schulze CH, Linsenmair KE, Fiedler K (2001) Understorey versus canopy: patterns of vertical stratification and diversity among Lepidoptera in a Bornean rain forest. Plant Ecol 153: 133–152

    Article  Google Scholar 

  • Schulze CH, Waltert M, Kessler PJA, Pitopang R, Shahabuddin, Veddeler D, Mühlenberg M, Gradstein SR, Leuschner C, Steffan-Dewenter I, Tscharntke T (2004) Biodiversity indicator groups of tropical land-use systems: comparing plants, birds, and insects. Ecol Appl 14: 1321–1333

    Google Scholar 

  • Scoble MJ (1995) The Lepidoptera: form, function, and diversity, 2nd ed. Oxford University Press, Oxford

    Google Scholar 

  • Scoble MJ (ed) (1999) Geometrid moths of the world — a catalogue (Lepidoptera: Geometridae). CSIRO Publishing, Collingwood

    Google Scholar 

  • Summerville KS, Ritter LM, Crist TO (2004) Forest moth taxa as indicators of lepidopteran richness and habitat disturbance: a preliminary assessment. Biol Conserv 116: 9–18

    Article  Google Scholar 

  • Süßenbach D (2003) Diversität von Nachtfaltergemeinschaften entlang eines Höhengradienten in Südecuador (Lepidoptera: Pyraloidea, Arctiidae). PhD thesis, Univ Bayreuth. URL: http://opus.ub.uni-bayreuth.de/volltexte/2003/33

    Google Scholar 

  • Tammaru T, Haukioja E (1996) Capital breeders and income breeders among Lepidoptera — consequences to population dynamics. Oikos 77: 561–564

    Article  Google Scholar 

  • Trueblood DD, Gallagher ED, Gould DM (1994) Three stages of seasonal succession on the Savin Hill Cove mudflat, Boston Harbor. Limnol Oceanogr 39: 1440–1454

    Article  Google Scholar 

  • Weller SJ, Jacobson NL, Conner WE (1999) The evolution of chemical defences and mating systems in tiger moths (Lepidoptera: Arctiidae). Biol J Linn Soc 68: 557–578

    Article  Google Scholar 

  • Williams-Linera G, Domínguez-Gastelú V, García-Zurita ME (1998) Microenvironment and floristics of different edges in a fragmented tropical rainforest. Conserv Biol 12: 1091–1102

    Article  Google Scholar 

  • Willott SJ (1999) The effects of selective logging on the distribution of moths in a Bornean rainforest. Phil Trans R Soc Lond B 354: 1783–1790

    Article  CAS  Google Scholar 

  • Wirooks L (2005) Die ökologische Aussagekraft des Lichtfangs — eine Studie zur Habitatbindung und kleinräumigen Verteilung von Nachtfaltern und ihren Raupen. Wolf & Kreuels, Havixbeck-Hohenholte

    Google Scholar 

  • Wong KM, Phillipps A (eds) (1996) Kinabalu: Summit of Borneo. Sabah Society with Sabah Parks, Kota Kinabalu

    Google Scholar 

  • Wright SJ (2005) Tropical forests in a changing environment. Trends Ecol Evol 20: 553–560

    Article  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 2007 Springer-Verlag Berlin Heidelberg

About this chapter

Cite this chapter

Fiedler, K., Hilt, N., Brehm, G., Schulze, C.H. (2007). Moths at tropical forest margins — how mega-diverse insect assemblages respond to forest disturbance and recovery. In: Tscharntke, T., Leuschner, C., Zeller, M., Guhardja, E., Bidin, A. (eds) Stability of Tropical Rainforest Margins. Environmental Science and Engineering. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-540-30290-2_3

Download citation

Publish with us

Policies and ethics