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Short-term effects of forest disturbances on soil nematode communities in European mountain spruce forests

Published online by Cambridge University Press:  10 October 2012

A. Čerevková ,
M. Renčo  and
L. Cagáň
A. Čerevková*
Affiliation:
Institute of Parasitology SAS, Hlinková 3, 040 01, Košice, Slovak Republic
M. Renčo
Affiliation:
Institute of Parasitology SAS, Hlinková 3, 040 01, Košice, Slovak Republic
L. Cagáň
Affiliation:
Slovak Agricultural University, A. Hlinku 2, 94 976, Nitra, Slovak Republic
*
* E-mail: [email protected]
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Abstract

The nematode communities in spruce forests were compared with the short-term effects of forest damage, caused by windstorm, wildfire and management practices of forest soils. Soil samples were collected in June and October from 2006 to 2008 in four different sites: (1) forest unaffected by the wind (REF); (2) storm-felled forest with salvaged timber (EXT); (3) modified forest affected by timber salvage (wood removal) and forest fire (FIR); and (4) storm-felled forest where timber had been left unsalvaged (NEX). Nematode analysis showed that the dominant species in all four investigated sites were Acrobeloides nanus and Eudorylaimus silvaticus. An increase of A. nanus (35% of the total nematode abundance) in the first year in the FIR site led to the highest total abundance of nematodes compared with other sites, where nematode abundance reached the same level in the third year. In the FIR site bacterial feeders appeared to be the most representative trophic group, although in the second and third year, after disturbance, the abundance of this trophic group gradually decreased. In the NEX site, the number of nematode species, population densities and Maturity Index were similar to that recorded for the FIR site. In EXT and NEX sites, the other dominant species was the plant parasitic nematode Paratylenchus microdorus. Analyses of nematodes extracted from different forest soil samples showed that the highest number of species and diversity index for species (H'spp) were in the REF site. Differences between the nematode fauna in REF and other localities were clearly depicted by cluster analysis. The greatest Structure Index and Enrichment Index values were also in REF. In the EXT site, the number of nematode species, their abundance, H'spp and Maturity Index were not significantly different from those recorded in the reference site.

Type
Research Papers
Information
Journal of Helminthology , Volume 87 , Issue 3 , September 2013 , pp. 376 - 385
Copyright
Copyright © Cambridge University Press 2012 

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References

Baermann, G. (1917) Eine einfache Methode zur Auffindung von Ankylostomum (Nematoden) Larven in Erdproben. Geneeskunde Tijdschrift Voor Nederlands Indië 57, 131–137.Google Scholar
Bjørlund, L., Vesterrgård, M., Johansson, S., Nyborg, M., Steffensen, L. & Christensen, S. (2002) Nematode communities of natural and managed beech forests – a pilot survey. Pedobiologia 46, 53–62.CrossRefGoogle Scholar
Bloemers, G.F., Hodda, M., Lambshead, P.J.D., Lawton, J.H. & Wanless, F.R. (1997) The effects of forest disturbance on diversity of tropical soil nematodes. Oecologia 111, 575–582.CrossRefGoogle ScholarPubMed
Bongers, T. (1988) De Nematoden van Nederland. 408 pp. Utrecht, Koninklijke Nederlandse Natuurhistorische Vereniging.Google Scholar
Bongers, T. (1990) The maturity index: an ecological measure of environmental disturbance based on nematode species composition. Oecologia 83, 14–19.CrossRefGoogle ScholarPubMed
Bongers, T. & Korthals, G. (1995) The behaviour of MI and PPI under enriched conditions. Nematologica 41, 286.Google Scholar
Čerevková, A. (2006) Nematode communities in three types of grassland in the Slovak Republic. Helminthologia 43, 171–176.CrossRefGoogle Scholar
Čerevková, A. & Renčo, M. (2009) Soil nematode community changes associated with windfall and wildfire in forest soil at the High Tatras National Park, Slovak Republic. Helminthologia 46, 123–130.CrossRefGoogle Scholar
Certini, G. (2005) Effect of fire on properties of forest soils: a review. Oecologia 143, 1–10.CrossRefGoogle ScholarPubMed
Donegan, K.K., Watrud, L.S., Seidler, R.J., Maggard, S.P., Shiroyama, T., Porteous, L.A. & DiGiovanni, G. (2001) Soil and litter organisms in Pacific northwest forest under different management practices. Applied Soil Ecology 18, 159–175.CrossRefGoogle Scholar
Fenster, M., Ferrick, C. & Scott, M. (2004) Fall burning does not affect nematode density or carbon and nitrogen levels in Iowa oak forest soils. Tillers 5, 9–12.Google Scholar
Ferris, H., Bongers, T. & De Goede, R.G.M. (2001) A framework for soil food web diagnostics: extension of the nematode faunal analysis concept. Applied Soil Ecology 18, 13–29.CrossRefGoogle Scholar
Fleischer, P. (2008) Windstorm research and monitoring in the High Tatra Mts., objectives, principles, methods, and current status. Contributions to Geophysics and Geodesy 38, 233–248.Google Scholar
Forge, T.A. & Simard, S.W. (2001) Structure of nematode communities in forest soils of southern British Columbia: relationships to nitrogen mineralization and effects of clearcut harvesting and fertilization. Biology and Fertility of Soils 34, 170–178.Google Scholar
Freckman, D.W. & Ettema, C.H. (1993) Assessing nematode communities in agroecosystems of varying human intervention. Agriculture, Ecosystems, Environment 45, 239–261.CrossRefGoogle Scholar
Gömöryová, E., Strělcová, K., Škvarenina, J., Bebej, J. & Gömöry, D. (2008) The impact of windthrow and fire disturbances on selected soil properties in the Tatra National Park. Soil and Water Research 3, 74–80.CrossRefGoogle Scholar
Gömöryová, E., Strělcová, K., Fleischer, P. & Gömöry, D. (2011) Soil microbial characteristics at the monitoring plots on windthrow areas of the Tatra National Park (Slovakia): their assessment as environmental indicators. Environmental Monitoring and Assessment 174, 31–45.CrossRefGoogle ScholarPubMed
Háněl, L. (2004) Response of soil nematodes inhabiting spruce forests in the Sumava Mountains to disturbance by bark beetles and clear-cutting. Forest Ecology and Management 202, 209–225.CrossRefGoogle Scholar
Matlack, G.R. (2001) Factors determining the distribution of soil nematodes in a commercial forest landscape. Forest Ecology and Management 146, 129–143.CrossRefGoogle Scholar
McSorley, R. (1993) Short-term effects of fire on the nematode community in a pine forest. Pedobiologia 37, 39–48.Google Scholar
Shannon, C.E. & Weaver, W. (1949) The mathematical theory of communication. 144 pp. Urbana, University of Illinois Press.Google Scholar
Šimonovičová, A., Hanajík, P., Lancuch, P., Mičuda, R., Hloško, M., Dlapa, P., Ferianc, P. & Haydenová, J. (2007) Pedochemical characteristics, soil microbiota and plant community changes in the High Tatras after windstorm (2005–2006) (in Slovak). in Fleischer, P. & Matejka, F. (Eds) Windstorm research in the High Tatras Mts. Proceedings of the conference, Tatranská Lomnica, 25–26 October. Bratislava, Geophysical Institute of the Slovak Academy of Sciences (CD-ROM).Google Scholar
Sohlenius, B. (1996) Structure and composition of the nematode fauna in pine forest soil under the influence of clear-cutting. Effects of slash removal and field layer vegetation. European Journal of Soil Biology 32, 1–14.Google Scholar
Sohlenius, B. (1997) Fluctuation of nematode populations in pine forest soil. Influence of clear-cutting. Fundamental and Applied Nematology 20, 103–114.Google Scholar
Sohlenius, B. (2002) Influence of clear-cutting and forest age on the nematode fauna in a Swedish pine forest soil. Applied Soil Ecology 19, 261–277.CrossRefGoogle Scholar
Soloveva, G.I. (1972) Parasitic nematodes of woody and herbabaceous plants. 134 pp. Washington, Agricultural Research Service, US Department of Commerce.Google Scholar
Šoltés, R., Školek, J. & Kyselová, Z. (2008) Developmet of vegetation after disaster (in Slovak). in Fleischer, P. & Matejka, F. (Eds) Windstorm research in the TANAP, 2008, 20–21 November 2008. Bratislava, Geophysical Institute of the Slovak Academy of Sciences (CD-ROM).Google Scholar
Southey, J.F. (1986) Laboratory methods for work with plant and soil nematodes. 202 pp. London, Her Majesty's Stationery Office.Google Scholar
StatSoft Inc (2001) Statistica Cz-Software system for data analysis, Release 6. Available at:http://www.statsoft.cz (accessed accessed July 2011).Google Scholar
Wasilewska, L. (1997) Soil invertebrates as bioindicators, with special reference to soil-inhabiting nematodes. Russian Journal of Nematology. 5, 113–126.Google Scholar
Yeates, G.W. (2007) Abundance, diversity, and resilience of nematode assemblages in forest soil. Canadian Journal of Forest Research 37, 216–225.CrossRefGoogle Scholar
Yeates, G.W. & Lee, W.G. (1997) Burning in a New Zealand snow-tussock grassland: effects on vegetation and soil fauna. New Zealand Journal of Ecology 21, 73–79.Google Scholar
Yeates, G.W., Bongers, T., De Goede, R.G.M., Freckman, D.W. & Georgieva, S.S. (1993) Feeding habits in nematode families and genera – an outline for soil ecologists. Journal of Nematology 25, 315–331.Google ScholarPubMed