Hostname: page-component-84b7d79bbc-fnpn6 Total loading time: 0 Render date: 2024-07-25T07:11:59.087Z Has data issue: false hasContentIssue false

Coexistence, Stress, and Catastrophe, in Grassy Vegetation Established in a Hard-limestone Quarry

Published online by Cambridge University Press:  24 August 2009

Jean M. Dixon
Affiliation:
Senior Experimental Officer and Senior Lecturer in Environmental Biology, respectively, Postgraduate School of Studies in Environmental Science, University of Bradford, Bradford BD7 1DP, England, UK.
David J. Hambler
Affiliation:
Senior Experimental Officer and Senior Lecturer in Environmental Biology, respectively, Postgraduate School of Studies in Environmental Science, University of Bradford, Bradford BD7 1DP, England, UK.

Extract

Plant communities produced experimentally in twometres' square plots on the rubble-covered floor of a limestone quarry showed changes in the cover values that were attributable to the sown grass and to immigrant mosses over a period of three years. Cover values for the mosses were lower in summer than in the following autumn over two cycles, whilst the cover that was attributable to the sown grass, a non-rhizomatous cultivar of Festuca rubra, did not follow a clear pattern. No evidence of directional change was found; this suggests a stable coexistence of the grass with mosses. It is suggested that one property of such a community will be a differentiation of regeneration niches which are favourable to an increase of diversity through immigration.

Episodic persistent flooding and consequent deposition of colloidal limestone on well-established and diversifying vegetation, followed by a single catastrophic incident of compression by the tyres of heavy vehicles, resulted in the loss of F. rubra and mosses, and the ascendency of a perennial survivor (Agrostis stolonifera).

Type
Main Papers
Copyright
Copyright © Foundation for Environmental Conservation 1988

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Allen, S.E., Carlisle, A., White, E.J. & Evans, C.C. (1968). The plant nutrient content of rainwater. Journal of Ecology, 56, pp. 497504, illustr.CrossRefGoogle Scholar
Al-Mufti, M.M., Sydes, C.L., Furness, S.B., Grime, J.P. & Band, S.R. (1977). A quantitative analysis of shoot phenology and dominance in herbaceous vegetation. Journal of Ecology, 65, pp. 759–91, illustr.CrossRefGoogle Scholar
Clarkson, D.T., Kuiper, P.J.C. & Luttge, U. (1986). Sources of nutrients for land plants from outside the pedosphere. Progress in Botany, 48, pp. 8096.CrossRefGoogle Scholar
Cole, V.C., Innis, G.S. & Stewart, J.W.B. (1977). Simulation of phosphorus cycling in semiarid grasslands. Ecology, 58(1), pp. 215, illustr.CrossRefGoogle Scholar
Davies, M.S. & Singh, A.K. (1983). Population differentiation in Festuca rubra L. and Agrostis stolonifera L. in response to soil waterlogging. New Phytologist, 94(4), pp. 573–83, illustr.CrossRefGoogle Scholar
Davis, B.N.K., Lakhani, K.H., Brown, M.C. & Park, D.G. (1985). Early serai communities in a limestone quarry: an experimental study of treatment effects on cover and richness of vegetation. Journal of Applied Ecology, 22(2), pp. 473–90, illustr.CrossRefGoogle Scholar
Dixon, J.M. & Hambler, D.J. (1984). An experimental approach to the reclamation of a limestone quarry floor: the first three years. Environmental Conservation, 11(1), pp. 1928, illustr.CrossRefGoogle Scholar
Eveling, D.W. & Bataillé, A. (1984). The effect of deposits of small particles on the resistance of leaves and petals to water loss. Environmental Pollution, Series A, 36, pp. 229–38.CrossRefGoogle Scholar
Grime, J.P. (1979). Plant Strategies and Vegetation Processes. John Wiley & Sons, Chichester, England, UK: xi + 222 pp., illustr.Google Scholar
Grime, J.P. & Hodgson, J.G. (1987). Botanical contributions to contemporary ecological theory. New Phytologist, 106 (Suppl.), pp. 283–95, illustr.CrossRefGoogle Scholar
Hambler, D.J. & Dixon, J.M. (1986). An experimental approach to the reclamation of a limestone quarry floor: the fourth to seventh years. Environmental Conservation, 13(4), pp. 337–45, illustr.CrossRefGoogle Scholar
Keizer, P.J., Tooren, B.F. van & During, H.J. (1985). Bryophytes and seedlings in chalk grassland. Journal of Ecology, 73(2), pp. 493504, illustr.CrossRefGoogle Scholar
Lee, R.B., (1988). Phosphate influx and extracellular phosphatase activity in barley roots and rose cells. New Phytologist, 109(2), pp. 141–8, illustr.CrossRefGoogle Scholar
Manning, W.J. (1971). Effects of limestone dust on leaf condition, foliar disease incidence and leaf surface microflora of native plants. Environmental Pollution, 2, pp. 6976, map.Google Scholar
Martinez, M.T., Romero, C. & Gavilan, J.M. (1984). Solubilization of phosphorus by humic acids from lignite. Soil Science, 138(4), pp. 257–61.CrossRefGoogle Scholar
Odum, E.P. (1971). Fundamentals of Ecology, 3rd edn.W.B. Saunders, Philadelphia, Pennsylvania, USA: xvi + 574 pp., illustr.Google Scholar
Tooren, B.F. van, Hertog, J. den & Verhaar, J. (1988). Cover, biomass and nutrient content of bryophytes in Dutch chalk grasslands. Lindbergia, 14, pp. 18, illustr.Google Scholar
Tukey, H.B. Jun., (1970). The leaching of substances from plants. Annual Review of Plant Physiology, 21, pp. 305–24.CrossRefGoogle Scholar