Hostname: page-component-586b7cd67f-l7hp2 Total loading time: 0 Render date: 2024-11-27T01:24:45.292Z Has data issue: false hasContentIssue false

Leaf Litter Decomposition of Nonnative Shrub Species in Nonnative and Native Shrub Environments: A Field Experiment with Three Rosaceae Shrubs

Published online by Cambridge University Press:  20 January 2017

Vojtěch Lanta*
Affiliation:
Section of Ecology, Department of Biology, University of Turku, Turku, Finland, FI-20014
Terho Hyvönen
Affiliation:
Plant Production Research, MTT Agrifood Research Finland, Jokioinen, Finland, FI-31600
Kai Norrdahl
Affiliation:
Section of Ecology, Department of Biology, University of Turku, Turku, Finland, FI-20014
*
Corresponding author's E-mail: [email protected]

Abstract

Invasion by nonnative plants may have ecosystem-wide effects, altering the decomposition rate of plant material via changes in litter quality or altered environment (abiotic conditions, associated biotic community), or both. Yet, the relative importance of these factors for decomposition rates is not clear. We studied decomposition using the leaves of related shrub species (nonnative Sorbaria sorbifolia and Rosa rugosa, native Rubus idaeus) with comparable physiognomy but different leaf characteristics and origin (alien vs. native) in patches formed by S. sorbifolia and Rubus idaeus in southwestern Finland. Decomposition of cellulose in the topsoils of the patches was also studied. Using litter bags, we found that S. sorbifolia leaf litter decomposed slowest and Rosa rugosa leaves fastest irrespective of patch type. Topsoils in S. sorbifolia patches were richer in carbon, nitrogen, and calcium than those of Rubus idaeus, but these differences did not affect decomposition rates. Very little decomposition appeared to happen during the winter but during the summer, microclimate had minor but significant effects on decomposition rates. Our results highlight the key role of litter source in the decomposition of plant material. Between-patch differences in abiotic conditions appear to play a minor role relative to litter quality.

Type
Research Article
Copyright
Copyright © Weed Science Society of America 

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

Literature Cited

Ashton, IW, Hyatt, LA, Howe, KM, Gurevitch, J, Lerdau, MT (2005) Invasive species accelerate decomposition and litter nitrogen loss in a mixed deciduous forest. Ecol Appl 15:12631272 Google Scholar
Belovsky, GE (1981) Food plant selection by a generalist herbivore: the moose. Ecology 62:10201030 Google Scholar
Boswell, CC, Espie, PR (1998) Uptake of moisture and nutrients by Hieracium pilosella and effects on soil in a dry sub-humid grassland. N Z J Agric Res 41:251261 Google Scholar
Bruun, HH (2005) Rosa rugosa Thunb. ex Murray. J Ecol 93:441470 Google Scholar
Butenschoen, O, Scheu, S, Eisenhauer, N (2011) Interactive effects of warming, soil humidity and plant diversity on litter decomposition and microbial activity. Soil Biol Biochem 43:19021907 Google Scholar
Coq, S, Souquet, JM, Meudec, E, Cheynier, V, Hattenschwiler, S (2010) Interspecific variation in leaf litter tannins drives decomposition in a tropical rain forest of French Guiana. Ecology 91:20802091 Google Scholar
Cornelissen, JHC, Pérez-Harguindeguy, N, Díaz, S, Grime, JP, Marzano, B, Cabido, M, Cerabolini, B (1999) Leaf structure and defence control litter decomposition rate across species and life forms in regional floras on two continents. New Phytol 143:191200 Google Scholar
Cornwell, WK, Cornelissen, JHC, Amatangelo, K, Dorrepaal, E, Eviner, VT, Godoy, O, Hobbie, SE, Hoorens, B, Kurokawa, H, Pérez-Harguindeguy, N, Quested, HM, Santiago, LS, Wardle, DA, Wright, IJ, Aerts, R, Allison, SD, Van Bodegom, P, Brovkin, V, Chatain, A, Callaghan, TV, Díaz, S, Garnier, E, Gurvich, DE, Kazakou, E, Klein, JA, Read, J, Reich, PB, Soudzilovskaia, NA, Vaieretti, MV, Westoby, M (2008) Plant species traits are the predominant control on litter decomposition rates within biomes worldwide. Ecol Lett 11:10651071 Google Scholar
D'Antonio, CM, Vitousek, PM (1992) Biological invasions by exotic grasses, the grass fire cycle, and global change. Ann Rev Ecol Evol Syst 23:6387 Google Scholar
Dassonville, N, Vanderhoeven, S, Vanparys, V, Hayez, M, Gruber, W, Meerts, P (2008) Impacts of alien plants on soil nutrients are correlated with initial site conditions in NW Europe. Oecologia 157:131140 Google Scholar
Davies, PJ, Gan, S (2012) Towards an integrated view of monocarpic plant senescence. Russ J Plant Physiol 59:467478 Google Scholar
Dehlin, H, Peltzer, DA, Allison, VJ, Yeates, GW, Nilsson, MC, Wardle, DA (2008) Tree seedling performance and belowground properties in stands of invasive and native tree species. N Z J Ecol 32:6769 Google Scholar
Ehrenfeld, JG (2003) Effects of exotic plant invasions on soil nutrient cycling processes. Ecosystems 6:503523 Google Scholar
Ehrenfeld, JG (2010) Ecosystem consequences of biological invasions. Ann Rev Ecol Evol Syst 41:5980 Google Scholar
Finland's National Strategy on Invasive Alien Species (2012) Ministry of Agriculture and Forestry in Finland, Helsinki. MMM – Invasive alien species http://www.mmm.fi/en/index/frontpage/natural_resources/invasive_alien_species.html. Accessed January 2014Google Scholar
Heneghan, L, Fatemi, F, Umek, L, Grady, K, Fagen, K, Workman, M (2006) The invasive shrub European buckthorn (Rhamnus cathartica L.) alters soil properties in midwestern US woodlands. Appl Soil Ecol 32:142148 Google Scholar
Hobbs, RJ, Mooney, HA (1986) Community changes following shrub invasion of grassland. Oecologia 70:508513 Google Scholar
Hunt, HW, Wall, DH (2002) Modeling the effects of loss of soil biodiversity on ecosystem function. Global Change Biol 8:3350 Google Scholar
Inderjit, van der Putten, WH (2010) Impacts of soil microbial communities on exotic plant invasions. Trends Ecol Evol 25:512519 Google Scholar
Inderjit, Wardle, DA, Karban, R, Callaway, RM (2011) The ecosystem and evolutionary contexts of allelopathy. Trends Ecol Evol 26:655662 Google Scholar
Kaspari, M, Garcia, MN, Harms, KE, Santana, M, Wright, SJ, Yavitt, JB (2008) Multiple nutrients limit litterfall and decomposition in a tropical forest. Ecol Lett 11:3543 Google Scholar
Kempel, A, Chrobock, T, Fischer, M, et al. (2013) Determinants of plant establishment success in a multispecies introduction experiment with native and alien species. Proc Natl Acad Sci U S A 110:1272712732 Google Scholar
Kim, DK, Zee, OP (2000) A new cyagenic glycoside from Sorbaria sorbifolia var. stepilla. Chem Pharm Bull 48:17661767 Google Scholar
Kotilainen, T, Haimi, J, Tegelberg, R, Julkunen-Tiitto, R, Vapaavuori, E, Aphalo, PJ (2009) Solar ultraviolet radiation alters alder and birch litter chemistry that in turn affects decomposers and soil respiration. Oecologia 161:719728 Google Scholar
Kourtev, P, Huang, W, Ehrenfeld, JG (1998) Effects of exotic plant species on soil properties in hardwood forests of New Jersey. Water Air Soil Pollut 105:493501 Google Scholar
Lanta, V, Hyvönen, T, Norrdahl, K (2013) Non-native and native shrubs have differing impacts on species diversity and composition of associated plant communities. Plant Ecol 214:15171528 Google Scholar
Liao, C, Peng, R, Luo, Y, Zhou, X, Wu, X, Fang, C, Chen, J, Li, B (2008) Altered ecosystem carbon and nitrogen cycles by plant invasion: a meta-analysis. New Phytol 177:706714 Google Scholar
Mack, RN, Simberloff, D, Lonsdale, WM, Evans, H, Clout, M, Bazzaz, FA (2000) Biotic invasions: causes, epidemiology, global consequences, and control. Ecol Appl 10:689710 Google Scholar
Martinson, HM, Schneider, K, Gilbert, J, Hines, JE, Hamback, PA, Fagan, WF (2008) Detritivory: stoichiometry of a neglected trophic level. Ecol Res 23:487491 Google Scholar
Morin, JP (1999) Community Ecology. London Wiley-Blackwell. 424 pGoogle Scholar
Nagai, T, Kawashima, T, Suzuki, N, Tanoue, Y, Kai, N, Nagashima, T (2007) Tea beverages made from Romanas rose (Rosa rugosa Thunb.) leaves possess strongly antioxidative activity by high contents of total phenols and vitamin C. J Food Agric Environ 5:137141 Google Scholar
Parsons, SA, Congdon, RA, Storlie, CJ, Shoo, LP, Williams, SE (2012) Regional patterns and controls of leaf decomposition in Australian tropical rainforests. Aust Ecol 37:845854 Google Scholar
Pérez-Harguindeguy, N, Diaz, S, Cornelissen, JHC, Vendramini, F, Cabido Castellanos, AM (2000) Chemistry and toughness predict leaf litter decomposition rates over a wide spectrum of functional types and taxa in central Argentina. Plant Soil 218:2130 Google Scholar
Pinheiro, JC, Bates, DM (2000) Mixed-Effects Models in S and S-plus. New York Springer. 528 pGoogle Scholar
Prescott, CE (2010) Litter decomposition: what controls it and how can we alter it to sequester more carbon in forest soils? Biogeochemistry 101:133149 Google Scholar
R Development Core Team (2013) R—A Language and Environment for Statistical Computing. http://www.R-project.org. Accessed November 2013Google Scholar
Raich, JW, Schlesinger, WH (1992) The global carbon dioxide flux in soil respiration and its relationship to vegetation and climate. Tellus 44B:8199 Google Scholar
Richardson, DM, Rejmánek, M (2011) Trees and shrubs as invasive species—a global review. Divers Distrib 17:788809 Google Scholar
Robinson, CH (2002) Controls on decomposition and soil nitrogen availability at high latitudes. Plant Soil 242:6581 Google Scholar
Skurski, TC, Maxwell, BD, Rew, LJ (2013) Ecological tradeoffs in non-native plant management. Biol Conserv 159:292302 Google Scholar
Staaf, H (1980) Influence of chemical composition, addition of raspberry leaves, and nitrogen supply on decomposition rate and dynamics of nitrogen and phosphorus in beech leaf litter. Oikos 35:5562 Google Scholar
Tabuchi, T, Hiramatsu, N, Hida, Y (2010) Anatomical characteristics of leaf mesophyll on Rosa rugosa and their hybrid plant. Acta Horticulturae 870:137142 Google Scholar
Thomas, H (2013) Senescense, ageing and death of the whole plant. New Phytol 197:696711 Google Scholar
Vilà, M, Espinar, JL, Hejda, M, Hulme, PE, Jarošík, V, Maron, JL, Pergl, J, Schaffner, U, Sun, Y, Pyšek, P (2011) Ecological impacts of invasive alien plants: a meta-analysis of their effects on species, communities and ecosystems. Ecol Lett 14:702708 Google Scholar
Vuorinen, J, Mäkitie, O (1955) The method of soil testing in use in Finland. Agrogeol Publ 63:144 Google Scholar
Wardle, DA, Bardgett, RD, Klironomos, JN, Setälä, H, van der Putten, WH, Wall, DH (2004) Ecological linkages between aboveground and belowground biota. Science 304:16291633 Google Scholar
Weidenhamer, JD, Callaway, RM (2010) Direct and indirect effects of invasive plants on soil chemistry and ecosystem function. J Chem Ecol 36:5969 Google Scholar
Wild, A (1993) Soils and Environment: An Introduction. Cambridge, UK: Cambridge University Press. 287 pGoogle Scholar