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Habitat edges are regarded as important components of heterogeneous landscapes. Diverse theories exist about the diversity and functional role of edges, and no generalisation have been possible so far, thus case studies are important for better understanding the landscape scale processes. Forest management highly modified the structure and tree species composition of the European forests. The sylvicultural intensification resulted in the rise of the proportion of non-native, intensively managed forest stands. In the present study we explore the response of spider and ant assemblages to forest stand type and the edge effect between native poplar and non-native conifer plantations in Hungary. We applied pitfall traps to sample the ground-dwelling spiders and ants. Four plots consisting of the two forest types and the transition zones between them were selected. Five transects for each replicated plot were sampled. We identified the significant indicator species of the different habitat types. We found significant differences in the species richness (i.e. number of species) of ants and spiders of the different habitat types. We detected intermediate spider species richness at the edge indicating that edges separate a higher quality habitat from one that has lower resource quality; however, the species richness of ants was the highest at the edge and did not differ between the two forest types. The positive impacts of edge was found due to presence of generalist and grassland species at the edge and presumably edges separate patches that provide complementary resources also increasing the number of ant species. Our results indicate that forest type affects the species compositions of ground-dwelling spiders and ants. Our study also shows that habitat type had a major effect on the species richness and composition of spider and ant assemblages, suggesting that local forestry management plays a crucial role in preserving the native invertebrate fauna of forests.
Czasopismo
Rocznik
Tom
Strony
815--820
Opis fizyczny
Bibliogr. 30 poz., rys., tab.
Twórcy
autor
- Department of Ecology, University of Szeged, H-6726 Szeged, Közép fasor 52.
autor
- Department of Ecology, University of Szeged, H-6726 Szeged, Közép fasor 52.
autor
- Department of Ecology, University of Szeged, H-6726 Szeged, Közép fasor 52.
autor
- Department of Ecology, University of Szeged, H-6726 Szeged, Közép fasor 52.
Bibliografia
- 1. Anderson M.J. 2001 – A new method for non-parametric multivariate analysis of variance – Austr. Ecol. 26: 32–46.
- 2. Banschbach V.S., Yeamans R., Brunelle A., Gulka A., Holmes M. 2012 – Edge Effects on Community and Social Structure of Northern Temperate Deciduous Forest Ants – Psyche, A.J. Entom. Article ID 548260.
- 3. Barbaro L., Pontcharraud L., Vetillard F., Guyon D., Jactel H. 2005 – Comparative responses of bird, carabid, and spider assemblages to stand and landscape diversity in maritime pine plantation forests – Ecoscience, 12: 110–121.
- 4. Bremer L.L., Farley K.A., 2010 – Does plantation forestry restore biodiversity or create green deserts? A synthesis of the effects of land-use transitions on plant species richness – Biodivers. Conserv. 19: 3893–3915.
- 5. Crawley M.J. 2007 – The R Book −John Wiley, New York, pp: 627–685.
- 6. Czechowski W., Radchenko A., Czechowska W., Vepsäläinen K. 2012 – The ants Hymenoptera: Formicidae of Poland with reference to the myrmecofauna of Europe – Natura Optima Dux Foundation, Warsaw.
- 7. Dąbrowska-Prot E. Wasiłowska A. 2012 – The role of ecotones in man-disturbed landscape: boundaries between mixed forest and adjacent man-made ecosystems in the Kampinos National Park, Poland – Pol. J. Ecol. 60: 677–698.
- 8. Didham R.K., Hammond P.M., Lawton J.H, Eggleton P., Stork N.E.. 1998 – Beetle species responses to tropical forest fragmentation – Ecol. Monog. 68: 295–323.
- 9. Dufrene M., Legendre P. 1997 – Species assemblages and indicator species: the need for a flexible asymetrical approach – Ecol. Monogr. 67: 345–366.
- 10. Erdős L., Bátori Z., Morschhauser T. Körmöczi L. 2013 – Ecological boundaries at different scales: vegetation pattern of the field layer in a south Hungarian mountain area – Pol. J. Ecol. 61: 319–328.
- 11. Finch O.D. 2005 – Evaluation of mature conifer plantations as secondary habitat for epigeic forest arthropods Coleoptera: Carabidae; Araneae – Forest Ecol. Manag. 204: 21–34.
- 12. Gallé R., Torma A. 2009 – Epigeic spider Araneae assemblages of natural forest edges in the Kiskunság Hungary – Community Ecol. 10: 146–151.
- 13. Gibb H., Parr C.L. 2010 – How does habitat complexity affect ant foraging success? A test using functional measures on three continents – Oecologia, 164: 1061–1073.
- 14. Gotelli N.J., Colwell R.K. 2001 – Quantifying biodiversity: procedures and pitfalls in the measurement and comparison of species richness. – Ecol. Lett. 4: 379–391.
- 15. Ivanov K., Keiper J. 2010 – Ant (Hymenoptera: Formicidae) diversity and community composition along sharp urban forest edges – Biodiv. Conserv. 19: 3917–3933.
- 16. Kotze D.J., Samways M.J. 1999 – Invertebrate conservation at the interface between the grassland matrix and natural Afromontane forest fragments – Biodiv. Conserv. 8: 1339–1363.
- 17. Kotze D.J, Samways M.J. 2001 – No general edge effect for invertebrates at Afromontane forest/grassland ecotones – Biodiv. Conserv. 10: 443–466.
- 18. Neuvonen S., Saikkonen T., Sundström L., Punttila P., Risch A.C., Domisch T., Niemela P., Kilpelainen J., Ohashi M., Finér L. 2012 – Stand type is more important than red wood ant abundance for the structure of ground‐dwelling arthropod assemblages in managed boreal forests – Agr. For. Entomol. 14: 295–305.
- 19. NiemeläJ., Haila Y., Halme E., Lahti T., Pajunen T., Punttila P. 1988 – The distribution of carabid beetles in fragments of old coniferous taiga and adjacent managed forest – Ann. Zool. Fenn. 25: 107–119.
- 20. Pryke J.S., Samways M.J. 2009 – Recovery of invertebrate diversity in a rehabilitated city landscape mosaic inthe heart of a biodiversity hotspot – Landscape Urban Plan, 93: 54–62.
- 21. Pryke J.S., Samways M.J. 2012 – Conservation of complex natural forest and plantation edge effects – Landscape Ecol. 27: 73–85.
- 22. Reznikova Z. Dorosheva H. 2004 – Impacts of red wood ants Formica polyctena on the spatial distribution and behavioural patterns of ground beetles (Carabidae) – Pedobiologia, 48: 15–21.
- 23. Ries L., Fletcher Jr.R.J., Battin J., Sisk T.D. 2004 – Ecological responses to habitat edges: mechanisms, models, and variability explained – Annu. Rev. Ecol. Evol. Syst. 35: 491–52.
- 24. Robson T.C., Baker A.C., Murray B.R. 2009 – Differences in leaf-litter invertebrate assemblages between radiata pine plantations and neighbouring native eucalypt woodland – Austr. Ecol. 34: 368–376.
- 25. Solymos R. 2000 – Afforestation Programmes in Hungary - A Story of Success (In: NEWFOR – New Forests for Europe: Afforestation at the Turn of the Century, European Forest Institute. Joensuu, Finland, Ed: N. Weber) −Frieburg, Germany, pp. 167–175.
- 26. Topping C.J., Luff M.L. 1995 – Three factors affecting the pitfall catch of linyphiid spiders Araneae: Linyphiidae – B. Brit. Arachnol. Soc. 10: 35–38.
- 27. Török K., Halassy M., Szabó R. 2003 – Restoration strategy for endemic grasslands in a low productive region of Hungary – Proceedings of the VIIth International Rangelands Congress, pp. 1132–1138.
- 28. Uetz G.W. 1991 – Habitat structure and spider foraging (In: Habitat Structure: The Physical Arrangement of Objects in Space. Eds: S.S. Bell, E.D. McCoy, H.R. Mushinsky) −Chapman and Hall, New York, pp. 325–348.
- 29. Yu X.D., Lou T.H., Zhou H.Z. 2010 – Distribution of ground-dwelling beetle assemblages Coleoptera across ecotones between natural oak forests and mature pine plantations in North China – J. Insect Conserv. 14: 617–626.
- 30. Wise D.H. 1993 – Spiders in Ecological Webs. Cambridge University Press, New York, pp: 1−328.
Typ dokumentu
Bibliografia
Identyfikator YADDA
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