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Influence of a non-native invasive tree on primary succession at Mt. Koma, Hokkaido, Japan

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Abstract

The slopes of Mt. Koma in Japan are undergoing primary succession as a result of a 1929 eruption. Understory vegetation below a non-native invasive tree species, Larix kaempferi, a native tree, Betula ermanii, and in the open were compared to determine if the non-native tree species was influencing species composition. Larix canopies are significantly larger than Betula canopies. Vegetation under Larix canopies had significantly greater richness and diversity than vegetation in the open, vegetation under Betula was intermediate but was significantly greater than the open in diversity. Vegetation cover was highest under Betula and significantly lower in the open. Larix canopy size was positively correlated with size and number of Salix reinii shrubs. Betula canopy size was positively correlated with size but not with number of Salix reinii shrubs. Species assemblages in the three sites are slightly different as shown by DCA. Due to the limited species pool on Mt. Koma the greatest possible extent of differences between the three microsites is not large. At this point Larix certainly appears to be accelerating succession for the non-tree species. If Larix persists on the slopes then succession would be permanently deflected towards a Larix forest. This would be a case of succession being deflected towards dominance by the introduced species.

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References

  • Belsky A.J. 1994. Influences of trees on savanna productivity: tests of shade, nutrients, and tree-grass competition. Ecology 75: 922–932.

    Article  Google Scholar 

  • Bertness M.D. and Callaway R.M. 1994. Positive interactions in communities: a post cold war perspective. Trends in Ecology and Evolution 9: 191–193.

    Article  Google Scholar 

  • Callaway R.M., Nadkarni N.M. and Mahall B.E. 1991. Facilitation and interference of Quercus douglasii on understory productivity in central California (USA). Ecology 72: 1484–1499.

    Article  Google Scholar 

  • Clarkson B.R. and Clarkson B.D. 1983. Mt. Tarawera 2. Rates of change in the vegetation and flora of the high domes. New Zealand Journal of Ecology 2: 107–119.

    Google Scholar 

  • Connell J.H. and Slatyer R.O. 1977. Mechanisms of succession in natural communities and their role in community stability and organization. American Naturalist 111: 1119–1144.

    Article  Google Scholar 

  • Dale V.D. 1991. Revegetation of Mount St. Helens debris avalanche 10 years post-eruptive. National Geographic Research and Exploration 7: 328–341.

    Google Scholar 

  • del Moral R. and Grishin S.Y. 1999. Volcanic disturbances and ecosystem recovery. In: Goodall D. and Walker L.R. (eds), Ecosystems of Disturbed Ground, Ecosystems of the World Series.Elsevier Scientific, Amsterdam, pp. 137–160.

    Google Scholar 

  • del Moral R. and Wood D.M. 1993. Early primary succession on the volcano Mount St. Helens. Journal of Vegetation Science 4: 223–234.

    Article  Google Scholar 

  • Hacker S.D. and Gaines S.D. 1997. Some implications of direct positive interactions for community species diversity. Ecology 89: 1990–2003.

    Article  Google Scholar 

  • Hill M.O. and Gauch H.G. 1980. Detrended Correspondence Analysis: an improved ordination technique. Vegetatio 42: 47–58.

    Article  Google Scholar 

  • Holmgren M., Scheffer M. and Huston M.A. 1997. The interplay of facilitation and competition in plant communities. Ecology 78: 1966–1975.

    Article  Google Scholar 

  • Holzapfel C. and Mahall B.E. 1999. Bi-directional facilitation and interference between shrubs and annuals in the Mojave Desert.Ecology 80: 1747–1761.

    Article  Google Scholar 

  • Jaccard S. 1912. The distribution of the flora of the alpine zone.New Phytologist 11: 37–50.

    Article  Google Scholar 

  • Kojima S. 1979. Biogeoclimatic zones of Hokkaido Island, Japan.Journal of College Liberal Arts, Toyama University, Natural Science Series 12: 97–141.

    Google Scholar 

  • Kondo T. and Tsuyuzaki S. 1999. Natural regeneration patterns of the introduced larch, Larix kaempferi (Pinaceae), on the volcano Mount Koma, northern Japan. Diversity and Distributions 5: 223–233.

    Article  Google Scholar 

  • McAuliffe J.R. 1984. Sahuaro-nurse tree associations in the Sonoran Desert: competitive effects of sahuaros. Oecologia 64: 319– 321.

    Article  Google Scholar 

  • McMurtrie R. and Wolf L. 1983. A model of competition between trees and grass for radiation, water and nutrients. Annals of Botany 52: 449–458.

    Google Scholar 

  • Morris W.F. and Wood D.M. 1989. The role of Lupinus lepidus in succession on Mount St. Helens: Facilitation or inhibition? Ecology 70: 697–703.

    Article  Google Scholar 

  • Norton D.A. 1992. Disruption of natural ecosystems by biological invasion. In: Willson J.H.M., Bondrup-Nielsen S., Drysdale C., Herman T.B., Munro N.W.P. and Pollock T.L. (eds), Science and Management of Protected Areas. Elsevier, Amsterdam, pp. 309–319.

    Google Scholar 

  • Pickett S.T.A., Collins S.L. and Armesto J.J. 1987. A hierarchical consideration of causes and mechanisms in succession. Vegetation 69: 109–114.

    Article  Google Scholar 

  • Reichard S.E. 1997. Prevention of invasive plant introduction on national and local levels. In: Luken J.O. and Thieret J.W. (eds), Assessment and Management of Plant Invasions. Springer-Verlag, New York, pp. 215–227.

    Google Scholar 

  • Rejmanek M. 1989. Invasibility of plant communities. In: Drake J.A., Mooney H.A., di Castri F., Groves R.H., Kruger F.J., Rejmanek M. et al. (eds), Biological Invasions – A Global Perspective.John Wiley, Chichester, UK, pp. 369–388.

    Google Scholar 

  • Richardson D.M. and Higgins S.I. 1998. Pine as invaders in the southern hemisphere. In: Richardson D.M. (ed.), Ecology and Biogeography of Pinus. Cambridge University Press, Cambridge, pp. 450–473.

    Google Scholar 

  • Rouget M., Richardson D.M., Milton S.J. and Polakow D. 2001.Predicting invasion dynamics of four alien Pinus species in a highly fragmented semi-arid shrubland in South Africa. Plant Ecology 152: 79–92.

    Article  Google Scholar 

  • Schlesinger W.H., Raikes J.A., Hartley A.E. and Cross A.F. 1996.On the spatial pattern of soil nutrients in desert ecosystems.Ecology 77: 364–374.

    Article  Google Scholar 

  • Shumway S.W. 2000. Facilitative effects of a sand dune shrub on species growing beneath the shrub canopy. Oecologia 124: 138–148.

    Article  Google Scholar 

  • Smathers G.A. and Mueller-Dombois D. 1974. Invasion and recovery of vegetation after a volcanic eruption in Hawaii. National Park Service Monograph Series 5. Government Printing Office, Washington, DC, USA.

    Google Scholar 

  • Tatewaki M., Ito K. and Tohyama M. 1965. Phytosociological study on forests of Japanese larch (Larix leptolepis Gordon).Research Bulletins of the College Experimental Forests. College of Agriculture, Hokkaido University, 1–176 (in Japanese with English summary).

  • ter Braak C.J.F. and Smilauer P. 1998. CANOCO reference manual and user's guide to CANOCO for Windows Software for Canonical Community Ordination (version 4). Microcomputer Power, Ithaca.

    Google Scholar 

  • Tewksbury J.J. and Lloyd J.D. 2001. Positive interactions under nurse-plants: spatial scale, stress gradients and benefactor size.Oecologia 127: 425–434.

    Article  Google Scholar 

  • Tielborger K. and Kadmon R. 2000. Temporal environmental variation tips the balance between facilitation and interference in desert plants. Ecology 81: 1544–1583.

    Article  Google Scholar 

  • Titus J.H. and del Moral R. 1998a. The role of mycorrhizal fungi and microsites in primary succession on Mount St. Helens.American Journal of Botany 85: 370–375.

    Article  Google Scholar 

  • Titus J.H. and del Moral R. 1998b. Seedling establishment in different microsites on Mount St. Helens,Washington, USA. Plant Ecology 134: 13–26.

    Article  Google Scholar 

  • Titus J.H., Moore S., Arnot M. and Titus P.J. 1998. Inventory of the vascular flora of the blast zone, Mount St. Helens, Washington.Madroño 45: 146–161.

    Google Scholar 

  • Titus J.H., Nowak R.S. and Smith S.D. 2002. Soil resource heterogeneity in the Mojave Desert, Nevada. Journal of Arid Environments (in press).

  • Tsuyuzaki S., Hase A., Niinuma H. and Hanada Y. 2000. List for seed plants on Mount Koma, Hokkaido, in 2000. Biological Materials 36: 1–6.

    Google Scholar 

  • Tsuyuzaki S., Titus J.H. and del Moral R. 1997. Seedling establishment patterns on the Pumice Plain, Mount St. Helens, Washington. Journal of Vegetation Science 8: 727–734.

    Article  Google Scholar 

  • Uemura S. 1993. Forests and plants of Hokkaido: global dynamics and ecology of mixed conifer-hardwood forest zone. In: Higashi S., Osawa A. and Kanagawa K. (eds), Biodiversity and Ecology in Northernmost Japan. Hokkaido University Press, Sapporo, pp. 21–35.

    Google Scholar 

  • Valiente-Banuet A. and Ezcurra E. 1991. Shade as a cause of the association between the cactus Neobuxbaumia tetetzo and the nurse plant Mimosa luisana in the Tehuacan Valley, Mexico.Journal of Ecology 79: 961–971.

    Article  Google Scholar 

  • Versfeld D.B. and van Wilgen B.W. 1986. Impact of woody aliens on ecosystem properties. In: Macdonald I.A.W., Kruger F.J. and Ferrar A.A. (eds), The Ecology and Management of Biological Invasions in Southern Africa. Oxford University Press, Cape Town, pp. 239–246.

    Google Scholar 

  • Vitousek P.M., D'Antonio C.M., Loope L.L. and Westbrooks R. 1996. Biological invasions as global environmental change.American Scientist 84: 468–478.

    Google Scholar 

  • Vitousek P.M. and Walker L.R. 1989. Biological invasion by Myrica faya in Hawaii: plant demography, nitrogen fixation, and ecosystem effects. Ecological Monographs 59: 247–265.

    Article  Google Scholar 

  • Walker B.H. and Noy-Meir I. 1982. Aspects of the stability and resilience of savanna ecosystem. In: Huntley B.J. and Walker B.H. (eds), Ecology of Tropical Savannas. Springer-Verlag, New York, pp. 556–590.

    Google Scholar 

  • Walker L.R., Thompson D.B. and Landau F.H. 2001. Experimental manipulations of fertile islands and nurse plant effects in the Mojave Desert, USA. Western North American Naturalist 61: 25–35.

    Google Scholar 

  • Walker L.R. and Vitousek P.M. 1991. An invader alters germination and growth of a native dominant tree in Hawai'i. Ecology 72: 1449–1455.

    Article  Google Scholar 

  • Wezel A., Rajot J.-L. and Herbrig C. 2000. Influence of shrubs on soil characteristics and their function in Sahelian agro-ecosystems in semi-arid Niger. Journal of Arid Environments 44: 383– 398.

    Article  Google Scholar 

  • Yoshii Y. 1932. Re vegetation of Volcano Komagatake after the great eruption in 1929. Botanical Magazine, Tokyo, 406.

    Google Scholar 

  • Yoshii Y. 1942. Plant communities on Mount Koma after eruption.Ecological Review, Sendai 8: 170–226.

    Google Scholar 

  • Yura H. 1988. Comparative ecophysiology of Larix kaempferi (Lamb.) Carr. and Abies veitchi Lindl. Ecological Research 3: 67–73.

    Article  Google Scholar 

  • Zar J.H. 1999. Biostatistical Analysis. 4th edn. Prentice-Hall, Englewood Cliffs, NJ, USA.

    Google Scholar 

Download references

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Titus, J.H., Tsuyuzaki, S. Influence of a non-native invasive tree on primary succession at Mt. Koma, Hokkaido, Japan. Plant Ecology 169, 307–315 (2002). https://doi.org/10.1023/A:1026081910749

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