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Spread Dynamics of Perennial Pepperweed (Lepidium latifolium) in Two Seasonal Wetland Areas

Published online by Cambridge University Press:  20 January 2017

Mark J. Renz*
Affiliation:
University of Wisconsin Madison, Department of Agronomy, Madison, WI 53706
Scott J. Steinmaus
Affiliation:
Cal Poly San Luis Obispo, Biological Sciences Department, San Luis Obispo, CA 93407
David S. Gilmer
Affiliation:
U.S. Geological Survey, Western Ecological Research Center, 6924 Tremont Road, Dixon, CA 95620
Joseph M. DiTomaso
Affiliation:
University of California, Department of Plant Sciences, Davis, CA 95616
*
Corresponding author's E-mail: [email protected]
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Abstract

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Perennial pepperweed is an invasive plant that is expanding rapidly in several plant communities in the western United States. In California, perennial pepperweed has aggressively invaded seasonal wetlands, resulting in degradation of habitat quality. We evaluated the rate and dynamics of population spread, assessed the effect of disturbance on spread, and determined the biotic and abiotic factors influencing the likelihood of invasion. The study was conducted at eight sites within two wetland regions of California. Results indicate that in undisturbed sites, spread was almost exclusively through vegetative expansion, and the average rate of spread was 0.85 m yr−1 from the leading edge. Spread in sites that were disked was more than three times greater than in undisturbed sites. While smaller infestations increased at a faster rate compared with larger populations, larger infestations accumulated more newly infested areas than smaller infestations from year to year. Stem density was consistently higher in the center of the infestations, with about 2.4 times more stems per square meter compared with the leading edge at the perimeter of the population. The invasion by perennial pepperweed was positively correlated with increased water availability but was negatively correlated with the cover of perennial and annual species. Thus, high cover of resident vegetation can have a suppressive effect on the rate of invasion, even in wetland ecosystems. On the basis of these results, we recommend that resident plant cover not be disturbed, especially in wet areas adjacent to areas currently infested with perennial pepperweed. For infested areas, management efforts should be prioritized to focus on controlling satellite populations as well as the leading edge of larger infestations first. This strategy could reduce the need for costly active restoration efforts by maximizing the probability of successful re-establishment of resident vegetation from the adjacent seedbank.

Type
Research
Creative Commons
Creative Common License - CCCreative Common License - BY
This is an Open Access article, distributed under the terms of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution, and reproduction in any medium, provided the original work is properly cited.
Copyright
Copyright © Weed Science Society of America

References

Literature Cited

Andrew, M. E. and Ustin, S. L. 2010. The effects of temporally variable dispersal and landscape structure on invasive species spread. Ecol. Appl. 20:593608.Google Scholar
Blank, R. and Young, J. A. 1997. Lepidium latifolium: influences on soil properties, rates of spread, and competitive stature. Pages 6980 in Brock, J. H., Wade, M., Pysek, P., and Green, D., eds. Plant Invasions: Studies from North America and Europe. Leiden, The Netherlands Backhuys Publishers.Google Scholar
Boyer, K. E. and Burdick, A. P. 2010. Control of Lepidium latifolium (perennial pepperweed) and recovery of native plants in tidal marshes of the San Francisco Estuary. Wetlands Ecol. Manage. 18:731743.Google Scholar
Chen, H., Qualls, R. G., and Miller, G. C. 2002. Adaptive responses of Lepidium latifolium to soil flooding: biomass allocation, adventitious rooting, aerenchyma formation and ethylene production. Environ. Exp. Bot. 48:119128.Google Scholar
Der, G. and Everitt, B. S. 2002. A Handbook of Statistical Analyses using SAS. 2nd ed. Boca Raton, FL Chapman and Hall/CRC Press. 376 p.Google Scholar
DiTomaso, J. M. and Healy, E. A. 2007. Weeds of California and Other Western States. Berkeley, CA University of California, Department of Agriculture and Natural Resources Publ. 3488. 2 Volumes. 1808 p.Google Scholar
Eiswerth, M., Johnson, W., Lewis, S., and Hughes, L. 2001. The economic costs of delaying invasive weed control: an illustration based on Nevada's tall whitetop initiative. University of Nevada, Reno Cooperative Extension Special Publication SP-01-08.Google Scholar
Gardner, C. M. 2002. Tall Whitetop, Lepidium latifolium: Response to Abiotic Conditions and Control Measures in the Intermountain West. M.S. thesis. Columbia, MO University of Missouri. Pp. 63108.Google Scholar
James, J. J., Smith, B. S., Vasquez, E., and Sheley, R. L. 2010. Principles for ecologically-based invasive plant management. Invasive Plant Sci. Manag. 3:229239.Google Scholar
Laubhan, M. K. and Shaffer, T. L. 2006. Seed germination of Cirsium arvense and Lepidium latifolium: implications for management of montane wetlands. Wetlands 26:6978.Google Scholar
Leininger, A. E. and Foin, T. C. 2009. Lepidium latifolium reproductive potential and seed dispersal along salinity and moisture gradients. Biol. Invasions 11:23512365.Google Scholar
Lepš, J. and Šmilauer, P. 2003. Multivariate Analysis of Ecological Data Using CANOCO. Cambridge, UK Cambridge University Press. 269 p.Google Scholar
Losure, D. A., Moloney, K. A., and Wilsey, B. J. 2009. Modes of crown vetch invasion and persistence. Am. Midl. Nat. 161:232242.Google Scholar
Lyeik, K. A. 1989. Lepidium latifolium L., a sea-shore species in Norway. Blyttia 47:109113.Google Scholar
Renz, M. J. 2005. Perennial pepperweed, Lepidium latifolium L. Pages 9198 in Duncan, C. L., and Clark, J. K., eds. Invasive Plants of Range and Wildlands and Their Environmental Economic and Societal Impacts. Lawrence, KS Weed Science Society of America.Google Scholar
Renz, M. J. and Blank, R. R. 2004. Influence of perennial pepperweed (Lepidium latifolium L.) biology and plant–soil relationships on management and restoration. Weed Technol. 18:13591364.Google Scholar
Renz, M. J. and DiTomaso, J. M. 2001. A comparison of control methods for perennial pepperweed within infestations of varying densities and the resulting impacts on resident plants populations. Proc. Calif. Weed Sci. Conf. 53:123.Google Scholar
Renz, M. J. and DiTomaso, J. M. 2004. Mechanism for the enhanced effect of mowing followed by glyphosate application to resprouts of perennial pepperweed (Lepidium latifolium). Weed Sci. 52:1423.Google Scholar
Renz, M. J. and DiTomaso, J. M. 2006. Early season mowing improves the effectiveness of chlorsulfuron and glyphosate for control of perennial pepperweed (Lepidium latifolium) with select herbicides. Weed Technol. 20:3236.Google Scholar
Renz, M. J., DiTomaso, J. M., and Schmierer, J. 1997. Above and belowground distribution of perennial pepperweed biomass and the utilization of mowing to maximize herbicide effectiveness. Proc. Calif. Weed Sci. Soc. 49:175.Google Scholar
Reynolds, L. K. and Boyer, K. E. 2010. Perennial pepperweed (Lepidium latifolium): properties of invaded tidal marshes. Invasive Plant Sci. Manag. 3:130138.Google Scholar
Robbins, W. W., Bellue, M. K., and Ball, W. S. 1951. Weeds of California. Sacramento California Department of Agriculture. 547 p.Google Scholar
Selleck, G. W. 1961. An ecological study of lens- and globe-podded hoary cress in Saskatchewan. Weeds. 13:15.Google Scholar
ter Braak, C. J. F. and Šmilauer, P. 2002. CANOCO reference manual and CanoDraw for Windows user's guide: software for canonical community ordination (version 4.5). Ithaca, NY Microcomputer Power.Google Scholar
Trumbo, J. 1994. Perennial pepperweed: a threat to wildland areas. Calif. Exotic Pest Plant Counc. Newsl. 2(3):45.Google Scholar
[USDA] U.S. Department of Agriculture. 1997. Management of Perennial Pepperweed (Tall Whitetop). Corvallis, OR USDA, Agricultural Research Service, Agriculture Experiment Station, Oregon State University Spec. Rept. 972. Pg. 42.Google Scholar
Weber, W. A. 1989. Additions to the flora of Colorado. Phytologia 67:429437.Google Scholar
Wilson, J. L., Ayres, D. R., Steinmaus, S., and Baad, M. 2009. Vegetation and flora of a biodiversity hotspot: Pine Hill, El Dorado County, California, USA. Madrono 56:246278.Google Scholar
Wilson, R. G., Boelk, D., Kyser, G. B., and DiTomaso, J. M. 2008. Integrated management of perennial pepperweed (Lepidium latifolium). Invasive Plant Sci. Manag. 1:1725.Google Scholar
Young, J. A., Palmquist, D. E., and Blank, R. R. 1998. The ecology and control of perennial pepperweed (Lepidium latifolium L.). Weed Technol. 12:402405.Google Scholar
Young, J. A., Palmquist, D. E., Blank, R. R., and Turner, C. E. 1995a. Ecology and control of perennial pepperweed (Lepidium latifolium L.). Pages 2931 in Lovich, J. E., Randall, R., and Kelly, M. D., eds. Berkeley, CA Proceedings of California Exotic Pest Plant Council.Google Scholar
Young, J. A., Palmquist, D. E., and Wotring, S. O. 1997. The invasive nature of Lepidium latifolium: a review. Pages 5968 in Brock, J. H., Wade, M., Pysek, P., and Green, D., eds. Plant Invasions: Studies from North America and Europe. Leiden, The Netherlands Backhuys Publishers.Google Scholar
Young, J. A., Turner, C. E., and James, L. F. 1995b. Perennial pepperweed. Rangelands 17:121123.Google Scholar