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Biogeochemistry of Plant Invasion: A Case Study with Downy Brome (Bromus tectorum)

Published online by Cambridge University Press:  20 January 2017

Robert R. Blank*
Affiliation:
United States Department of Agriculture–Agricultural Research Service, Exotic and Invasive Weed Research Unit, 920 Valley Road, Reno, NV 89512
*
Corresponding author's email: blank@unr.nevada.edu

Abstract

Limited data exist on the affect of downy brome invasion on biogeochemical cycling. Biogeochemical cycling was quantified in a winterfat community in northeastern, CA that was separated into three invasion classes: noninvaded (NI), invaded for 3 yr (I3), and 10 yr (I10) by downy brome. On each plot, all aboveground vegetation was harvested and separated by species, dried, weighed, and tissue nutrients quantified. In addition, soil samples were collected from 0- to 30-, 30- to 60-, and 60- to 100-cm depths and various nutrient pools quantified. Aboveground biomass g/m2 was significantly greater, with downy brome averaging over 90% of the plant mass on the I10 plots (280 g) compared to the NI plots (148 g). In comparison to the NI plots, vegetation fluxes (g/m2/yr) of carbon (C) were significantly greater, and fluxes of Ca, Fe, and Cu were significantly less on I10 plots. Soils occupied for 10 yr by downy brome have significantly greater total N and organic C, and greater availability of Fe, Mn, Cu, ortho-P, Ca, and K compared to NI soil. For the I10 plots, available soil N (dominantly NO3) was greatest in the 60- to 100-cm-depth increment, whereas for the other plots, N availability was greatest in the 0- to 30-cm-depth increment. Net N soil mineralization potential was near 0 on the I10 plots at all depth increments. These data suggest that invasion by downy brome facilitates elevated nutrient availability, possibly increases system leakiness of N, and fosters differential plant nutrient cycling relative to a native noninvaded community. Elevated nutrient availability promulgated by downy brome invasion might increase its competitive stature. Long-term occupation of environments by downy brome might affect the vertical distribution of nutrients, which can alter soil evolution and plant successional patterns.

Type
Case Study
Copyright
Copyright © Weed Science Society of America 

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References

Literature Cited

Barnett, J. F. and Crawford, J. A. 1994. Pre-laying nutrition of sage grouse hens in Oregon. J. Range Manage 47:114118.Google Scholar
Belnap, J. and Phillips, S. L. 2001. Soil biota in an ungrazed grassland: response to annual grass (Bromus tectorum) invasion. Ecol. Appl 11:12611275.CrossRefGoogle Scholar
Benson, L. V. 1978. Fluctuations in the level of pluvial Lake Lahontan during the last 40,000 years. Quat. Res 9:300318.CrossRefGoogle Scholar
Blank, R. R. 2005. Plant-soil relationships of Bromus tectorum: monitoring an invasion for five years. Abstracts, Annual Meeting of the Soil Science Society of America, Salt Lake City, Utah.Google Scholar
Blank, R. R., Allen, F., and Young, J. A. 1994. Extractable anions in soils following wildfire in a sagebrush-grass community. Soil Sci. Soc. Am. J 58:564570.Google Scholar
Blank, R. R. and Young, J. A. 2002. Influence of the exotic invasive crucifer, Lepidium latifolium, on soil properties and elemental cycling. Soil Sci 167:821829.Google Scholar
Booth, M. S., Stark, J. M., and Caldwell, M. M. 2003. Inorganic N turnover and availability in annual- and perennial-dominated soil in a northern Utah shrub-stepp ecosystem. Biogeochem 66:311330.CrossRefGoogle Scholar
Bradley, B. A., Houghton, R. A., Mustard, J. F., and Hamburg, S. P. 2006. Invasive grass reduces aboveground carbon stocks in shrublands of the Western US. Global Change Biol 12:18151822.Google Scholar
Bradley, M. A. and Mustard, J. F. 2005. Identifying land cover variability distinct from land cover change: cheatgrass in the Great Basin. Remote Sensing Environ 94:204213.CrossRefGoogle Scholar
Bundy, L. G. and Meisinger, J. J. 1994. Nitrogen availability indices. Pages 951984. in Weaver, chair, R. W., et al, editor. Methods of Soil Analysis, Part 2: Microbiological and Biochemical Properties. Madison, WI Soil Science Society of America.Google Scholar
Crooks, J. A. 2002. Characterizing ecosystem-level consequences of biological invasions: the role of ecosystem engineers. Oikos 97:153166.Google Scholar
D'Antonio, C. M. and Vitousek, P. M. 1992. Biological invasion by exotic grasses, the grass/fire cycle, and global change. Ann. Rev. Ecol. Syst 23:6387.CrossRefGoogle Scholar
Ehrenfeld, J. G. 2003. Effects of exotic plant invasion on soil nutrient cycling processes. Ecosystems 6:503523.Google Scholar
Englund, S. R. 2004. Bromus tectorum impacts soil carbon storage in semiarid grasslands of Canyonlands National Park. M.S. Thesis. Salt Lake City, UT University of Utah. 156.Google Scholar
Hamilton, E. W. III, Douglas, A., and Frank, D. A. 2001. Can plants stimulate soil microbes and their own nutrient supply. Evidence from a grazing tolerant grass. Ecol 82:23972402.Google Scholar
Jobbágy, E. G. and Jackson, R. B. 2001. The distribution of soil nutrients with depth: global patterns and the imprint of plant. Biogeochem 53:5177.Google Scholar
Jobbágy, E. G. and Jackson, R. B. 2004. The uplift of soil nutrients by plants: biogeochemical consequences across scales. Ecol 85:23802389.CrossRefGoogle Scholar
Jenny, H. 1941. Factors of Soil Formation: A System of Quantitative Pedology. New York, NY McGraw-Hill. 271.Google Scholar
Kalra, Y. P., editor. 1998. Handbook of Reference Methods for Plant Analysis. Boca Raton, FL CRC Press. 300.Google Scholar
Kelly, E. F., Chadwick, O. A., and Hilinski, T. E. 1998. The effect of plants on mineral weathering. Biogeochem 42:2153.Google Scholar
Levine, J. M., Vil, M., D'Antonio, C. M., Dukes, J. S., Grigulis, K., and Lavorel, S. 2003. Mechanisms underlying the impacts of exotic plant invasions. Proc. R. Soc. Biol. Sci. Ser. B 270:775781.Google Scholar
Lindsay, W. L. and Norvell, W. A. 1978. Development of a DTPA soil test for zinc, iron, manganese, and copper. Soil Sci. Soc. Am. J 42:421428.Google Scholar
Mack, R. N., Simberloff, D., Lonsdale, W. M., Evans, H., Clout, M., and Bazzaz, F. A. 2000. Biotic invasions: causes, epidemiology, global consequences, and control. Ecol. Appl 10:689710.Google Scholar
Melgoza, G., Nowak, R. S., and Tausch, R. J. 1990. Soil water exploration after fire: competition between Bromus tectorum (cheatgrass) and two native species. Oecologia 83:713.Google Scholar
Miles, J. 1985. The pedogenic effects of different species and vegetation types and the implications of succession. J. Soil Sci 36:571584.Google Scholar
Mitchell, J. E., West, N. E., and Miller, R. W. 1966. Soil physical properties in relation to plant community patterns in the shadscale zone of northwestern Utah. Ecology 47:627630.Google Scholar
Mozingo, H. N. 1987. Shrubs of the Great Basin: A Natural History. Reno, NV University of Nevada Press. 342.Google Scholar
Mubarek, A. and Olsen, R. A. 1976. Immiscible displacement of the soil solution by centrifugation. Soil Sci. Soc. Am. J 40:329331.Google Scholar
Norton, J. B., Monaco, T. A., Norton, J. M., Johnson, D. A., and Jones, T. A. 2004. Soil morphology and organic matter dynamics under cheatgrass and sagebrush-steppe plant communities. J. Arid Environ 57:445466.Google Scholar
Obrist, D., Delucia, E. H., and Arnone, J. A. III. 2003. Consequences of wildfire on ecosystem CO2 and water vapour fluxes in the great basin. Global Change Biol 9:563574.Google Scholar
Pellant, M. and Reichert, L. 1984. Management and rehabilitation of a burned winterfat community in southwestern Idaho. Pages 281285. in. A. R. Tiedemann, E. D. McArthur, H. C. Stutz, and others, compilers. Proceedings of the Symposium on the Biology of Atriplex and Related Chenopods; May 2–6 1983; Provo, UT. General Technical Report INT-172. Ogden, UT U.S. Department of Agriculture, Forest Service, Intermountain Forest and Range Experiment Station.Google Scholar
Quideau, S. A., Graham, R. C., Chadwick, O. A., and Wood, H. B. 1999. Biogeochemical cycling of calcium and magnesium by Ceanothus and Chamise. Soil Sci. Soc. Amer. J 63:18801888.Google Scholar
Rimer, R. L. and Evans, R. D. 2006. Invasion of downy brome (Bromus tectorum L.) causes rapid changes in the nitrogen cycle. Amer. Midl. Nat 156:252258.Google Scholar
Rodin, L. E. and Bazilevich, N. I. 1967. Production and Mineral Cycling in Terrestrial Vegetation. Edinburgh, Scotland, United Kingdom Oliver and Boyd. 288.Google Scholar
Sperry, L. J., Belnap, J., and Evans, R. D. 2006. Bromus tectorum invasion alters nitrogen dynamics in an undisturbed arid grassland ecosystem. Ecol 87:603615.Google Scholar
Stone, E. L. 1975. Effects of species on nutrient cycles and soil change. Phil. Trans. R. Soc. Lond. B 271:149162.Google Scholar
Ström, L. 1997. Root exudation of organic acids: importance to nutrient availability and the calcifuge and calcicole behaviour of plants. Oikos 80:459466.Google Scholar
Ulery, A. L., Graham, R. C., Chadwick, O. A., and Wood, H. B. 1995. Decade-scale changes of soil carbon, nitrogen, and exchangeable cations under chaparral and pine. Geoderma 65:121134.Google Scholar
Van Breemen, N. and Finzi, A. C. 1998. Plant-soil interactions: Ecological aspects and evolutionary implications. Biogeochem 42:119.Google Scholar
Vandenhoeven, S., Dassonville, N., and Meerts, P. 2005. Increased topsoil mineral nutrient concentrations under exotic invasive plants in Belgium. Plant Soil 275:169179.Google Scholar
Verburg, P. S. J., Arnone, J. A. III, Obrist, D., Schorran, D. E., Evans, R. D., Leroux-Swarthout, D., Johnson, D. W., Luo, Y., and Coleman, J. S. 2004. Net ecosystem carbon exchange in two experimental grassland ecosystems. Global Change Biol 10:498508.Google Scholar
Vitousek, P. M., D'Antonio, C. M., Loope, L. L., Rejmanek, M., and Westbrook, R. 1997. Introduced species: a significant component of human-caused global change. N. Z. J. Ecol 21:116.Google Scholar