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Change in disturbance regime facilitates invasion by Bellucia pentamera Naudin (Melastomataceae) at Gunung Palung National Park, Indonesia

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Abstract

In tropical rainforests, gaps created by fallen canopy trees are the primary colonization sites for pioneer species. Selective logging mimics these natural disturbances in that only a single tree is felled, creating a gap of comparable size. Rates of tree felling greatly exceed natural mortality rates, however, changing disturbance regime by increasing the number of gaps in logged areas compared to intact forest. Little is known about whether gaps in logged forests are qualitatively different as well. At Gunung Palung National Park in West Kalimantan, Indonesia, a period of selective logging in areas adjacent to the research station created a natural experiment permitting comparison of populations of the invasive pioneer tree Bellucia pentamera in selectively logged and undisturbed forest. We sought to first establish whether canopy gaps are necessary for invasion by B. pentamera. We then examined whether the type of gap (logging vs. natural treefall) had an effect on recruitment. Finally, we compared populations in natural treefall gaps in logged and undisturbed forest to estimate the effect of logging on population size. Bellucia pentamera was limited to gaps, regardless of canopy tree density. Furthermore, gaps created by selective logging supported significantly more B. pentamera individuals than natural gaps. Finally, natural treefall gaps in the disturbed area contained significantly more individuals than gaps in the undisturbed forest. Therefore, it appears that selective logging not only created more gaps for B. pentamera, these gaps in particular promoted greater abundance of this invader and led to a population increase throughout the disturbed habitat.

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References

  • Allcock KG, Hik DS (2003) What determines disturbance-productivity-diversity relationships? The effect of scale, species and environment on richness patterns in an Australian woodland. Oikos 102:173–185

    Google Scholar 

  • Barton K (2012) MuMIn: multi-model inference. R package version 0.12.2. http://r-forge.r-project.org/projects/mumin/

  • Belote RT et al (2012) Compositional stability and diversity of vascular plant communities following logging disturbance in Appalachian forests. Ecol Appl 22:502–516

    PubMed  Google Scholar 

  • Bicknell J, Struebig M, Davies Z (2015) Reconciling timber extraction with biodiversity conservation in tropical forests using reduced-impact logging. J Appl Ecol 52:379–388

    PubMed  PubMed Central  Google Scholar 

  • Brokaw N (1985) Gap-phase regeneration in a tropical forest. Ecology 66:682–687

    Google Scholar 

  • Brokaw N (1987) Gap-phase regeneration of three pioneer species in a tropical forest. J Ecol 75:9–19

    Google Scholar 

  • Burnham K, Anderson D (2002) Model selection and multi-model inference: a practical information-theoretic approach. Springer, New York

    Google Scholar 

  • Catford JA et al (2012) The intermediate disturbance hypothesis and plant invasions: implications for species richness and management. Perspect Plant Ecol Evolut Syst 14:231–241

    Google Scholar 

  • Cox RD, Allen EB (2008) Stability of exotic annual grasses following restoration efforts in southern California coastal sage scrub. J Appl Ecol 45:495–504

    Google Scholar 

  • Davis M, Grime J, Thompson K (2000) Fluctuating resources in plant communities: a general theiry of invasibility. J Ecol 88:528–534

    Google Scholar 

  • de Kok R, Briggs M, Pirnanda D, Girmansyah D (2015) Identifying targets for plant conservation in Harapan rainforest, Sumatra. Trop Conserv Sci 8:28–32

    Google Scholar 

  • Delnatte C, Meyer JY (2012) Plant introduction, naturalization, and invasion in French Guiana. Biol Invasions 14:915–927

    Google Scholar 

  • Denslow J (1987) Tropical rainforest gaps and tree species diversity. Ann Rev Ecol Syst 18:431–451

    Google Scholar 

  • Dorough JW et al (2007) From plant neighbourhood to landscape scales: how grazing modifies native and exotic plant species richness in grassland. Plant Ecol 191:185–198

    Google Scholar 

  • Funk JL, Vitousek PM (2007) Resource-use efficiency and plant invasion in low-resource systems. Nature 446:1079–1081

    PubMed  CAS  Google Scholar 

  • Gorchov D, Thompson E, O’Neil J, Whigham D, Noe D (2011) Treefall gaps required for establishment, but not survival, of invasive Rubus phoenicolasius in deciduous forest, Maryland, USA. Plant Species Biol 26:221–234

    Google Scholar 

  • Grime JP (1977) Evidence for existence of three primary strategies in plants and its relevance to ecological and evolutionary theory. Am Nat 111:1169–1194

    Google Scholar 

  • Hester A, Hobbs R (1992) Influence of fire and soil nutrients on native and non-native annuals at remnant vegetation edges in the Western Australian wheat-belt. J Veg Sci 3:101–108

    Google Scholar 

  • Hobbs R, Huenneke L (1992) Disturbance, diversity and invasion: implications for conservation. Conserv Biol 6:324–337

    Google Scholar 

  • Jauni M, Gripenberg S, Ramula S (2015) Non-native plant species benefit from disturbance: a meta-analysis. Oikos 124:122–129

    Google Scholar 

  • Johnson J, Omland K (2004) Model selection in ecology and evolution. Trends Ecol Evol 19:101–108

    PubMed  Google Scholar 

  • Joshi C (2006) Mapping cryptic invaders and invasibility of tropical forest ecosystems: Chromolaena odorata in Nepal. PhD Dissertation, University of Wageningen, The Netherlands

  • Lake JC, Leishman MR (2004) Invasion success of exotic plants in natural ecosystems: the role of disturbance, plant attributes and freedom from herbivores. Biol Conserv 117:215–226

    Google Scholar 

  • Lockwood JL, Hoopes MF, Marchetti MP (2007) Invasion ecology. Blackwell Publishing, Oxford

    Google Scholar 

  • Lozon J, MacIsaac H (1997) Biological invasions: are they dependent on disturbance? Environ Rev 5:131–144

    Google Scholar 

  • Marshall AJ (2004) Population ecology of gibbons and leaf monkeys across a gradient of Bornean forest types. PhD Dissertation, Harvard University, Cambridge, MA

  • Marshall AJ (2010) Effect of habitat quality on primate populations in Kalimantan: Gibbons and leaf monkeys as case studies. In: Gursky S, Supriatna J (eds) Indonesian primates. Springer, New York, pp 157–177

    Google Scholar 

  • Marshall AJ, Leighton M (2006) How does food availability limit the population density of white bearded gibbons? In: Hohmann G, Robbins MM, Boesch C (eds) Feeding ecology in apes and other primates: Ecological, physical, and behavioral aspects. Cambridge University Press, Cambridge, pp 313–335

    Google Scholar 

  • Marshall AJ, Beaudrot L, Wittmer HU (2014) Responses of primates and other frugivorous vertebrates to plant resource variability over space and time at Gunung Palung National Park. Int J Primatol 35:1178–1201

    Google Scholar 

  • Moles A et al (2012) Invasions: the trail behind, the path ahead, and a test of a disturbing idea. J Ecol 100:116–127

    Google Scholar 

  • R Development Core Team (2012) R: a language and environment for statistical computing. R Foundation for Statistical Computing, Vienna, Austria

    Google Scholar 

  • Reinhart K, Gurnee J, Tirado R et al (2006) Invasion through quantitative effects: intense shade drives native decline and invasive success. Ecol Appl 16:1821–1831

    PubMed  Google Scholar 

  • Rejmánek M (1996) Species richness and resistance to invasions. In: Orians GH, Dirzo R, Cushman JH (eds) Diversity and processes in tropical forest ecosystems. Springer, Berlin, pp 153–172

    Google Scholar 

  • Rejmánek M, Richardson D (1996) What attributes make some plant species more invasive? Ecology 77:1655–1661

    Google Scholar 

  • Renner S (1986) Reproductive biology of Bellucia (Melastomataceae). Acta Amazon 16(17):197–208

    Google Scholar 

  • Renner S (1989) Systematic studies in the Melastomataceae. Mem N Y Bot Garden 50:2–97

    Google Scholar 

  • Renner S (1990) Reproduction and Evolution in some genera of Neotropical Melastomataceae. Mem N Y Bot Garden 55:143–152

    Google Scholar 

  • Rutten G, Ensslin A, Hemp A, Fischer M (2015) Forest structure and composition of previously selectively logged and non-logged montane forests at Mt. Kilimanjaro. For Ecol Manag 337:61–66

    Google Scholar 

  • Silk J, Verburg R, Kebler P (2002) Effects of fire and selective logging on the stree species composition of lowland dipterocarp forest in East Kalimantan, Indonesia. Biodivers Conserv 11:85–98

    Google Scholar 

  • Smart N, Hatton J, Spence C (1985) The effect of long-term exclusion of large herbivores on vegetation in Murchison Falls National Park, Uganda. Biol Conserv 33:229–245

    Google Scholar 

  • Totland O, Nyeko P, Bjerknes AL, Hegland S, Nielsen A (2005) Does forest gap size affect population size, plant size, reproductive success and pollinator visitation in Lantana camara, a tropical invasive shrub? For Ecol Manag 215:329–338

    Google Scholar 

  • Villela D, Nascimento M, de Aragao L, da Gama D (2006) Effect of selective logging on forest structure and nutrient cycling in a seasonally dry Brazilian Atlantic Forest. J Biogeogr 33:506–516

    Google Scholar 

  • Xu H, Li Y, Liu S, Zang R, He F, Spence J (2015) Partial recovery of a tropical rainforest a half-century after clear-cut and selective logging. J Appl Ecol 52:1044–1052

    Google Scholar 

  • Yamada T, Hosaka T, Okuda T, Kassim AR (2013) Effects of 50 years of selective logging on demography of trees in a Malaysian lowland forest. For Ecol Manag 310:531–538

    Google Scholar 

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Acknowledgements

Permission to conduct research at Gunung Palung National Park was kindly granted by the Indonesian Institute of Sciences (LIPI), the State Ministry of Research and Technology (RISTEK), the Directorate General for Nature Conservation (PHKA) and the Gunung Palung National Park Bureau (BTNGP). CD would like to thank his research counterpart in Indonesia, Irwan Lovadi at Universitas Tanjungpura (UNTAN). This work was supported by grants from the British Ecological Society and the Davis Botanical Society. CD received support from a National Science Foundation Graduate Research Fellowship. CD would also like to thank his field assistants Sudi and Bacong for their help with this project. CD is also grateful for help and advice received from assistants at the Cabang Panti Research Station, as well as S.M. Jaffe, and lodging provided by AJM.

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Correspondence to Christopher Dillis.

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Dillis, C., Marshall, A.J. & Rejmánek, M. Change in disturbance regime facilitates invasion by Bellucia pentamera Naudin (Melastomataceae) at Gunung Palung National Park, Indonesia. Biol Invasions 19, 1329–1337 (2017). https://doi.org/10.1007/s10530-016-1345-5

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