Skip to main content
Log in

Demography and mobility of three common understory butterfly species from tropical rain forest of Papua New Guinea

  • Original article
  • Published:
Population Ecology

Abstract

The mobility of butterflies determines their ability to find host plant species, and thus their potential host plant range, as well as their ability to maintain meta-populations in fragmented habitats. While butterfly movement has been extensively studied for temperate species, very little is known for tropical forest species. A mark-release-recapture study of the three most common butterfly species in the understory of a lowland primary rainforest in Papua New Guinea included 3,705, 394 and 317 marked individuals of Danis danis, Taenaris sp. and Parthenos aspila respectively, with 1,031, 78 and 40 butterfly individuals recaptured at least once. Over a period of 6 weeks there were almost 22,000 individuals belonging to these three species hatching within or entering our four study plots totaling 14.58 ha in area. The most abundant species, D. danis, with 20,000 individuals, showed highly variable population densities during the study. The residency time in the studied plots was highest for P. aspila (84 days), as individual butterflies stayed mostly in a single gap; we estimated that less than 1 % of individuals disperse 1 km or more. Similar movement probability was found in D. danis whilst in Taenaris sp., 10 % of the population disperses ≥1 km. Movement distances of D. danis were more than sufficient to locate its host plant, Derris elliptica, which occurred in 61 % of the 20 × 20 m subplots within a 50 ha plot. Compared with temperate species, our three species have much longer life spans, but their movement patterns remain within the known mobility estimates of temperate species. The mobility of D. danis is close to the average for temperate Lycaenidae, while Taenaris sp. is more mobile and P. aspila less mobile than the mean for all temperate species.

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

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Institutional subscriptions

Fig. 1
Fig. 2
Fig. 3

Similar content being viewed by others

References

  • Arnold RA (1983) Ecological studies of six endangered butterflies (Lepidoptera, Lycaenidae): Island biogeography, patch dynamics, and the design of habitat preserves. University of California publications in entomology 99. University of California Press, Berkeley

  • Baguette M, Clobert J, Schtickzelle N (2011) Metapopulation dynamics of the bog fritillary butterfly: experimental changes in habitat quality induced negative density-dependent dispersal. Ecography 34:170–176

    Article  Google Scholar 

  • Baker M, Nur N, Geupel GR (1995) Correcting biased estimates of dispersal and survival due to limited study area: theory and an application using wrentits. Condor 97:663–674

    Article  Google Scholar 

  • Barbosa P, Segarra AE, Gross P, Caldas A, Ahlstrom K, Carlson RW, Ferguson DC, Grissell EE, Hodges RW, Marsh PM, Poole RW, Schauff ME, Shaw SR, Whitfield JB, Woodley NE (2001) Differential parasitism of macrolepidopteran herbivores on two deciduous tree species. Ecology 82:698–704

    Article  Google Scholar 

  • Basset Y, Eastwood R, Sam L, Lohman DJ, Novotny V, Treuer T, Miller SE, Weiblen GD, Pierce NE, Bunyavejchewin S, Sakchoowong W, Kongnoo P, Osorio-Arenas MA (2011) Comparison of rainforest butterfly assemblages across three biogeographical regions using standardized protocols. J Res Lepid 44:17–28

    Google Scholar 

  • Basset Y, Eastwood R, Sam L, Lohman DJ, Novotny V, Treuer T, Miller SE, Weiblen GD, Pierce NE, Bunyavejchewin S, Sakchoowong W, Kongnoo P, Osorio-Arenas MA (2012) Cross-continental comparisons of butterfly assemblages in tropical rainforests: implications for biological monitoring. Insect Conserv Divers 6:223–233

    Article  Google Scholar 

  • Beck J, Fiedler K (2009) Adult life spans of butterflies (Lepidoptera: Papilionoidea + Hesperioidea): broadscale contingencies with adult and larval traits in multi-species comparisons. Biol J Linn Soc 96:166–184

    Article  Google Scholar 

  • Beirao MV, Campos-Neto FC, Pimenta IA, Freitas AVL (2012) Population biology and natural history of Parides burchellanus (Papilionidae: Papilioninae: Troidini), an endangered Brazilian butterfly. Ann Entomol Soc Am 105:36–43

    Article  Google Scholar 

  • Benedick S, Hill JK, Mustaffa N, Chey VK, Maryati M, Searle JB, Schilthuizen M, Hamer KC (2006) Impacts of rain forest fragmentation on butterflies in northern Borneo: species richness, turnover and the value of small fragments. J Appl Ecol 43:967–977

    Article  Google Scholar 

  • Bonebrake TC, Ponisio LC, Boggs CL, Ehrlich PR (2010) More than just indicators: a review of tropical butterfly ecology and conservation. Biol Conserv 143:1831–1841

    Article  Google Scholar 

  • Brakefield PM (1982) Ecological studies on the butterfly Maniola jurtina in Britain. I. Adult behaviour, microdistribution and dispersal. J Anim Ecol 51:713–726

    Article  Google Scholar 

  • Clobert J, Lebreton JD (1985) Dépendance de facteurs de milieu dans les estimations de taux de survie par capture–recapture. Biometrics 41:1031–1037 (in French with English summary)

    Article  Google Scholar 

  • Connell JH (1971) On the role of natural enemies in preventing competitive exclusion in some marine animals and in rain forest trees. In: Den Boer PJ, Gradwell G (eds) Dynamics of populations. Centre for Agricultural Publishing and Documentation, Wageningen, pp 298–312

    Google Scholar 

  • Conradt L, Roper TJ, Thomas CD (2001) Dispersal behaviour of individuals in metapopulations of two British butterflies. Oikos 95:416–424

    Article  Google Scholar 

  • Cook LM, Brower LP, Croze HJ (1967) The accuracy of a population estimation from multiple recapture data. J Anim Ecol 36:57–60

    Article  Google Scholar 

  • Cook LM, Thomason EW, Young AM (1976) Population structure, dynamics and dispersal of the tropical butterfly Heliconius charitonius. J Anim Ecol 45:851–863

    Article  Google Scholar 

  • Corbet AS (1942) Fruit-baiting for Lepidoptera in the Eastern Tropics. Entomol 75:219–221

    Google Scholar 

  • Davis GAN, Frazer JFD, Tynan AM (1958) Population numbers in a colony of Lysandra bellargus Rott. (Lepidoptera: Lycaenidae) during 1956. Proc R Entomol Soc Lond Ser A Gen Entomol 33:31–36

    Google Scholar 

  • de-Andrade RB, Freitas AVL (2005) Population biology of two species of Heliconius (Nymphalidae: Heliconiinae) in a semi-deciduous forest in Southeastern Brazil. J Lepid Soc 59:223–228

    Google Scholar 

  • DeVries PJ, Murray D, Lande R (1997) Species diversity in vertical, horizontal, and temporal dimensions of a fruit-feeding butterfly community in an Ecuadorian rainforest. Biol J Linn Soc 62:343–364

    Article  Google Scholar 

  • Dicke M, Sabelis MW, Takabayashi J, Bruin J, Posthumus MA (1990) Plant strategies of manipulating predatorprey interactions through allelochemicals: prospects for application in pest control. J Chem Ecol 16:3091–3118

    Article  CAS  PubMed  Google Scholar 

  • Dixon AFG, Kindlmann P, Leps J, Holman J (1987) Why there are so few species of aphids, especially in the tropics. Am Nat 129:580–592

    Article  Google Scholar 

  • Ehrlich PR, Gilbert LE (1973) Population structure and dynamics of the tropical butterfly Heliconius ethilla. Biotropica 5:69–82

    Article  Google Scholar 

  • Fermon H, Waltert M, Larsen TB, Dall’Asta U, Mühlenberg M (2000) Effects of forest management on diversity and abundance of fruit-feeding nymphalid butterflies in south-eastern Côte d’Ivoire. J Insect Conserv 4:173–189

    Article  Google Scholar 

  • Fermon H, Waltert M, Mühlenberg M (2003) Movement and vertical stratification of fruit-feeding butterflies in a managed West African rainforest. J Insect Conserv 7:7–19

    Article  Google Scholar 

  • Francini RB, Freitas AVL, Brown KS Jr (2005) Rediscovery of Actinote zikani (D’Almeida) (Nymphalidae, Heliconiinae, Acraeini): natural history, population biology and conservation of an endangered butterfly in SE Brazil. J Lepid Soc 59:134–142

    Google Scholar 

  • Freitas AVL (1996) Population biology of Heterosais edessa (Nymphalidae) and its associated Atlantic Forest Ithomiinae community. J Lepid Soc 50:273–289

    Google Scholar 

  • Freitas AVL, Vasconcellos-Neto J, Vanini F, Trigo JR, Brown KS Jr (2001) Population studies of Aeria olena and Tithorea harmonia (Nymphalidae, Ithomiinae) in Southeastern Brazil. J Lepid Soc 55:150–157

    Google Scholar 

  • Hill CJ (1995) Linear strips of rain forest vegetation as potential dispersal corridors for rain forest insects. Conserv Biol 9:1559–1566

    Article  Google Scholar 

  • Hill JK, Hamer KC, Tangah J, Dawood M (2001) Ecology of tropical butterflies in rainforest gaps. Oecologia 128:294–302

    Article  Google Scholar 

  • Hovestadt T, Nowicki P (2008) Investigating movement within irregularly shaped patches: analysis of mark-release-recapture data using randomization procedures. Israel Journal of Ecology & Evolution 54:137–154

    Article  Google Scholar 

  • Janzen DH (1970) Herbivores and the number of tree species in tropical forests. Am Nat 104:501–528

    Article  Google Scholar 

  • Keller EC Jr, Mattoni RHT, Seiger MSB (1966) Preferential return of artificially displaced butterflies. Anim Behav 14:197–200

    Article  PubMed  Google Scholar 

  • Kessler A, Baldwin IT (2001) Defensive function of herbivore-induced plant volatile emissions in nature. Science 291:2141–2144

    Article  CAS  PubMed  Google Scholar 

  • Korosi A, Orvossy N, Batary P, Kover S, Peregovits L (2008) Restricted within-habitat movement and time-constrained egg laying of female Maculinea rebeli butterflies. Oecologia 156:455–464

    Article  PubMed  Google Scholar 

  • Kunte K (2008) Competition and species diversity: removal of dominant species increases diversity in Costa Rican butterfly communities. Oikos 117:69–76

    Article  Google Scholar 

  • Lebreton JD, Burnham KP, Clobert J, Anderson DR (1992) Modelling survival and testing biological hypotheses using marked animals—a unified approach with case studies. Ecol Monogr 62:67–118

    Article  Google Scholar 

  • Leonard JW (1939) Notes on the use of Derris as a fish poison. Trans Am Fish Soc 68:269–280

    Article  Google Scholar 

  • Lewis OT (2001) Effect of experimental selective logging on tropical butterflies. Conserv Biol 15:389–400

    Article  Google Scholar 

  • Lill JT, Marquis RJ, Ricklefs RE (2002) Host plants influence parasitism of forest caterpillars. Nature 417:170–173

    Article  CAS  PubMed  Google Scholar 

  • Mallet J (1986) Dispersal and gene flow in a butterfly with home range behavior: Heliconius erato (Lepidoptera: Nymphalidae). Oecologia 68:210–217

    Article  Google Scholar 

  • Marin L, Leon-Cortes JL, Stefanescu C (2009) The effect of an agro-pasture landscape on diversity and migration patterns of frugivorous butterflies in Chiapas, Mexico. Biodivers Conserv 18:919–934

    Article  Google Scholar 

  • Marini-Filho OJ, Martins RP (2010) Nymphalid butterfly dispersal among forest fragments at Serra da Canastra National Park, Brazil. J Insect Conserv 14:401–411

    Article  Google Scholar 

  • Molleman F, Kop A, Brakefield PM, DeVries PJ, Zwaan BJ (2006) Vertical and temporal patterns of biodiversity of fruit feeding butterflies in a tropical forest in Uganda. Biodivers Conserv 15:107–121

    Article  Google Scholar 

  • Molleman F, Zwaan BJ, Brakefield PM, Carey JR (2007) Extraordinary long life spans in fruit-feeding butterflies can provide window on evolution of life span and aging. Exp Gerontol 42:472–482

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  • Nowicki P, Richter A, Glinka U, Holzschuh A, Toelke U, Henle K, Woyciechowski M, Settele J (2005) Less input same output: simplified approach for population size assessment in Lepidoptera. Popul Ecol 47:203–212

    Article  Google Scholar 

  • Orr A, Kitching R (2010) The butterflies of Australia. Allen & Unwin, Sydney

    Google Scholar 

  • Parsons M (1999) The butterflies of Papua New Guinea: their systematics and biology. Academic Press, London

    Google Scholar 

  • Ramos RR, Freitas AVL (1999) Population biology and wing color variation in Heliconius erato phyllis (Nymphalidae). J Lepid Soc 53:11–21

    Google Scholar 

  • Sam L (2009) Composition of butterfly communities (Lepidoptera) along a successional gradient in a lowland rainforest of Papua New Guinea. B.Sc. thesis, University of Papua New Guinea

  • Schneider C (2003) The influence of spatial scale on quantifying insect dispersal: an analysis of butterfly data. Ecol Entomol 28:252–256

    Article  Google Scholar 

  • Schtickzelle N, Baguette M, Boulenge EL (2003) Modelling insect demography from capture–recapture data: comparison between the constrained linear models and the Jolly–Seber analytical method. Can Entomol 135:313–323

    Article  Google Scholar 

  • Scott JA (1973) Lifespan of butterflies. J Res Lepid 12:225–230

    Google Scholar 

  • Sekar S (2012) A meta analysis of the traits affecting dispersal ability in butterflies: can wingspan be used as a proxy? J Anim Ecol 81:174–184

    Article  PubMed  Google Scholar 

  • Spitzer K, Novotny V, Tonner M, Leps J (1993) Habitat preferences, distribution and seasonality of the butterflies (Lepidoptera, Papilionidea) in a montane tropical rain forest, Vietnam. J Biogeogr 20:109–121

    Article  Google Scholar 

  • Tufto J, Lande R, Ringsby T-H, Engen S, Sæther B-E, Walla TR, DeVries PJ (2012) Estimating Brownian motion dispersal rate, longevity and population density from spatially explicit mark–recapture data on tropical butterflies. J Anim Ecol 81:756–769

    Article  PubMed  Google Scholar 

  • Turner JRG (1971) Experiments on the demography of tropical butterflies. II. Longevity and home-range behaviour in Heliconius erato. Biotropica 3:21–31

    Article  Google Scholar 

  • Uehara-Prado M, Brown KS Jr, Freitas AVL (2005) Biological traits of frugivorous butterflies in a fragmented and a continuous landscape in the south Brazilian Atlantic forest. J Lepid Soc 59:96–106

    Google Scholar 

  • Vlasanek P, Sam L, Novotny V (2013) Dispersal of butterflies in a New Guinea rainforest: using mark–recapture methods in a large, homogeneous habitat. Ecol Entomol 38:560–569

    Article  Google Scholar 

  • Wang RJ, Ovaskainen O, Cao YD, Chen HQ, Zhou Y, Xu CR, Hanski I (2011) Dispersal in the Glanville fritillary butterfly in fragmented versus continuous landscapes: comparison between three methods. Ecol Entomol 36:251–260

    Article  Google Scholar 

  • White GC, Burnham KP (1999) Program Mark: survival estimation from populations of marked animals. Bird Study 46(Supplement):120–139

    Article  Google Scholar 

  • Wolda H (1988) Insect seasonality: why? Annu Rev Ecol Syst 19:1–18

    Article  Google Scholar 

  • Wright JS (2002) Plant diversity in tropical forests: a review of mechanisms of species coexistence. Oecologia 130:1–14

    Article  Google Scholar 

Download references

Acknowledgments

We thank Samuel Jepi, Christopher Saldon, Absolom Paul, Fidelis Kimbeng and numerous field assistants who helped with fieldwork. Wanang community, lead by Philip Damen, permitted this work on their lands. Billy Bau determined Derris species. Jan Leps advised on statistical analyses. Zdenek Faltynek Fric and Martin Konvicka commented on the manuscript. Tom M. Fayle and Nichola Plowman improved the English in the manuscript. This work was supported by the Christensen Fund, National Science Foundation (DEB-0841885), Czech Science Foundation (14-04258S), Czech Ministry of Education (LH11008), Darwin Initiative for the Survival of Species (UK), Grant Agency of the University of South Bohemia in Ceske Budejovice (121/2010/P, 136/2010/P) and by the project Biodiversity of forest ecosystems CZ.1.07/2.3.00/20.0064 co-financed by the European Social Fund and the state budget of the Czech Republic.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Petr Vlasanek.

Electronic supplementary material

Below is the link to the electronic supplementary material.

Supplementary material 1 (PDF 53 kb)

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Vlasanek, P., Novotny, V. Demography and mobility of three common understory butterfly species from tropical rain forest of Papua New Guinea. Popul Ecol 57, 445–455 (2015). https://doi.org/10.1007/s10144-015-0480-7

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10144-015-0480-7

Keywords

Navigation