Skip to main content
Log in

Changes in the seasonal rhythm of two forest communities during secondary succession

  • Published:
Biologia Aims and scope Submit manuscript

Abstract

Changes in the seasonal rhythm of two plant phytocoenoses in a submountain beech forest during secondary succession were studied. Investigations were done on four monitoring plots with different stand density over the period of four successive years. The rhythm of the associations Dentario bulbiferae-Fagetum and Carici pilosae-Fagetum reflects the course of succession processes running six years after the human impact (cutting) in the ecosystem. Results of the phenological observations of the understorey species with the focus on the changes in flowering and colour spectrum allowed to make the comparisons between both associations in connection with different phyto-climatic conditions and in dependence on time. The most conspicuous changes in the seasonal rhythm and structure of the examined associations were found in conditions of the former clear-cut, currently in succession phase. A clear decrease (56%) in number of taxons with the dominance > 1% in one association towards the end of the 4-year study period was detected here. Simultaneously, a decrease in the number of flowering species was observed, while the relative rate of species being in the vegetative stage increased considerably (from 6 to 67%) over the growing season. The course of flowering of both of the associations missed discernible trends and peaks as well as colour spectra were partially changed during four monitored successive years on the formerly unstocked area.

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.

Similar content being viewed by others

References

  • Abe T. & Kamo K. 2003. Seasonal changes of floral frequency and composition of flower in two cool temperate secondary forest in Japan. For. Ecol. Manag. 175: 153–162.

    Article  Google Scholar 

  • Barna M. 2004. Adaptation of European beech (Fagus sylvatica L.) to different ecological conditions: leaf size variation. Pol. J. Ecol. 52: 35–45.

    Google Scholar 

  • Battey N.H. 2000. Aspects of seasonality. J. Exp. Bot. 51: 1769–1780.

    Article  PubMed  CAS  Google Scholar 

  • Bottlíková A. 1975. Fenologická charakteristika vybraných fytocenóz Liptovskej kotliny. Biologické práce, 81 pp.

  • Bossuyt B. & Hermy M. 2000. Restoration of the understorey layer of recent forest bordering ancient forest. Appl. Veg. Sci. 3: 43–50.

    Article  Google Scholar 

  • Brunet J. & Oheimb G.V. 1998. Migration of vascular plants to secondary woodlands in southern Sweden. J. Ecol. 86: 429–438.

    Article  Google Scholar 

  • Davis M.A., Wrage K.J. & Reich P.B. 1998. Competition between tree seedlings and herbaceous vegetation: support for theory of resource supply and demand. J. Ecol. 86: 652–661

    Article  Google Scholar 

  • Diekmann M. 1996. Relationship between flowering phenology of perennial herbs and meteorological data in deciduous forests of Sweden. Can.J. Bot. 74: 528–537.

    Article  Google Scholar 

  • Eliáš P. 1987. Size inequality in coenopopulations of a woodland annual Impatients noli-tangere L. Biológia, Bratislava, 42: 881–891.

    Google Scholar 

  • Falińska K. 1975. Badania fenologiczne jako metoda ekologicznej analizy ekosystemóv. Wiadomości Ekologiczne 21: 213–232.

    Google Scholar 

  • Hull J.C. 2002. Photosynthetic induction dynamics to sunflecks of four deciduous forest understory herbs with different phenologies. Int. J. Plant Sci. 163: 913–924.

    Article  Google Scholar 

  • Kawarasaki S. & Hori Y. 2001. Flowering phenology of understory herbaceous species in a cool temperate deciduous forest in Ogawa Forest Reserve, central Japan. J. Plant Res. 114: 19–23.

    Article  Google Scholar 

  • Kikuzawa K. 2003. Phenological and morphological adaptations to the light environment in two woody and two herbaceous plant species. Fun. Ecol. 17: 29–38.

    Article  Google Scholar 

  • Kodrík M. 1997. Height diversity and species biomass on a clear felling site in conditions of a submontane beech forest. Folia dendrologica 24: 39–45.

    Google Scholar 

  • Kontriš J., Kontrišová O. & Gregor J. 1993. Dynamics of the phytocenoses development of the submountain beech forest stands. I. Phytococenoses. Ekológia, Bratislava, 12: 417–428.

    Google Scholar 

  • Kubíček F. & Šimonovič V. 1975. Dynamics and phenology of the total biomass of the herbaceous layer in two forest communities. Biológia, Bratislava, 30: 505–522.

    Google Scholar 

  • Kukla J., Kontriš J., Kontrišová O., Gregor J. & Mihálik A. 1998. Causes of floristical differentiation of Dentario bulbiferae-Fagetum (Zlatník 1935) Hartmann 1953 and Carici pilosae-Fagetum Oberd.1957 associations. Ekológia, Bratislava, 17: 177–186.

    Google Scholar 

  • Lapin M., Faško P., Melo M., Št’astný P. & Tomlain J. 2002. Klimatické oblasti. In: Miklos, L. (ed), Atlas krajiny Slovenskej republiky. MŽP, Bratislava, CD.

    Google Scholar 

  • Lieberman D. 1982. Seasonality and phenology in a dry tropical forest in Ghana. J. Ecol. 70: 791–806.

    Article  Google Scholar 

  • Lieth H. 1974. Phenology and seasonality modeling. Ecological studies 8. Springer-Verlag, New York, 444 pp.

    Google Scholar 

  • Marhold K. & Hindák F. 1998. Checklist of non-vascular and vascular plants of Slovakia. VEDA, Bratislava, 687 pp.

    Google Scholar 

  • Pykälä J. 2004. Immediate increase in plant species richness after clear-cutting of boreal herb-rich forests. App. Veg. Scien. 7: 29–34.

    Article  Google Scholar 

  • Ritter E., Dalsgaard L. & Einhorn K.S. 2005. Light, temperature and soil moisture regimes following gap formation in a semi-natural beech-dominated forest in Denmark. For. Ecol. Manag. 206: 15–33

    Article  Google Scholar 

  • Routier M.C. & Lapointe L. 2002. Impact of tree leaf phenology on growth rates and reproduction in the spring flowering species Trilium erectum (Liliaceae). Amer. J. Bot. 89: 500–505.

    Google Scholar 

  • Sakai S. 2001. Phenological diversity in tropical forests. Pop. Ecol. 43: 77–86.

    Article  Google Scholar 

  • Schieber B. 1996. Vplyv zakmenenia na fenológiu Dentaria bulbifera L. v assoc. Dentario bulbiferae-Fagetum (Zlatník 1935) Hartmann 1970, pp.77–80. In: Eliáš (ed.), Populačná biológia rastlín IV, SEKOS, Bratislava.

    Google Scholar 

  • Schwartz M.D. 1992. Phenology and springtime surface-layer change. Amer. Met. Soc. 120: 2570–2578.

    Google Scholar 

  • Sierra G.G., Merino A.P. & Herrero E.A. 1996. Phenology of Hyacinthoides non-scripta (L.) Chouard, Melittis melissophyllum and Symphytum tuberosum L. in 2 deciduous forests in the Cantabrian Mts, northwest Spain. Vegetatio 122: 69–82.

    Article  Google Scholar 

  • Střelec J. 1992. Vplyv ťažbového zásahu v bukovom poraste na zmeny osvetlenia. Lesnícky časopis 38: 551–558.

    Google Scholar 

  • Tyler G. 2001. Relationships between climate and flowering of eight herbs in a Swedish deciduous forest. Ann. Bot. 87: 623–630.

    Article  Google Scholar 

  • Wielgolaski F.E. 1999. Starting dates and basic temperatures in phenological observations of plants. Int. J. Biom. 42: 158–168.

    Article  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Schieber, B. Changes in the seasonal rhythm of two forest communities during secondary succession. Biologia 62, 416–423 (2007). https://doi.org/10.2478/s11756-007-0081-9

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.2478/s11756-007-0081-9

Key words

Navigation