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Effect of Lonicera maackii on Soil Carbon and Nitrogen in Southwestern Ohio Forests

Published online by Cambridge University Press:  20 January 2017

Sarah E. Kolbe ,
Amy Townsend-Small ,
Arnold I. Miller ,
Theresa M. Culley  and
Guy N. Cameron
Sarah E. Kolbe
Affiliation:
Department of Geology, University of Cincinnati, Cincinnati OH 45221
Amy Townsend-Small
Affiliation:
Department of Geology, University of Cincinnati, Cincinnati OH 45221
Arnold I. Miller
Affiliation:
Department of Geology, University of Cincinnati, Cincinnati OH 45221
Theresa M. Culley
Affiliation:
Department of Biological Sciences, University of Cincinnati, Cincinnati OH 45221
Guy N. Cameron*
Affiliation:
Department of Biological Sciences, University of Cincinnati, Cincinnati OH 45221
*
Corresponding author's E-mail: g.cameron@uc.edu
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Abstract

Introduced plants threaten biodiversity and ecosystem processes, including carbon (C) and nitrogen (N) cycles, but little is known about the threshold at which such effects occur. We examined the impact of the invasive shrub Amur honeysuckle on soil organic carbon (SOC) and N density at study sites that varied in invasion history. In plots with and without honeysuckle, we measured honeysuckle abundance and size (basal area) and extracted soil cores. SOC and N densities were highest at the site with the longest invasion history and highest invasion intensity (i.e., greatest abundance and basal area of honeysuckle). Basal area of honeysuckle positively affected SOC and N densities likely because of increased litter decomposition and altered microbial communities. Because honeysuckle increases forest net primary productivity (NPP) and SOC, it also may play a role in C sequestration. Our results demonstrate the need to consider the influence of invasion history and intensity when evaluating the potential impact of invasive species.

Keywords

Amur honeysuckleLonicera maackii (Rupr.) Herder LOMA6Amur honeysuckledeciduous forestinvasion historyinvasion intensityinvasive plantssoil nutrients
Type
Research Article
Information
Invasive Plant Science and Management , Volume 8 , Issue 4 , December 2015 , pp. 375 - 384
Copyright
Copyright © Weed Science Society of America 

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References

Literature Cited

Allison, SD, Vitousek, PM (2004) Rapid nutrient cycling in leaf litter from invasive plants in Hawai'i. Oecologia 141:612–619 CrossRefGoogle ScholarPubMed
Arthur, MA, Bray, SR, Kuchle, CR, McEwan, RW (2012) The influence of the invasive shrub, Lonicera maackii, on leaf decomposition and microbial community dynamics. Plant Ecol 213:1571–1582 Google Scholar
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 15:1263–1272 CrossRefGoogle Scholar
Asner, GP, Archer, S, Hughes, RF, Ansley, RJ, Wessman, CA (2003) Net changes in regional woody vegetation cover and carbon storage in Texas drylands, 1937–1999. Glob Change Biol 9:316–335 CrossRefGoogle Scholar
Blair, BC, Stowasser, A (2009) Impact of Lonicera maackii on decomposition rates of native leaf litter in a southwestern Ohio woodland. Ohio J Sci 109:43–47 Google Scholar
Blank, RR, Young, JA (1997) Lepidium latifolium: influences on soil properties, rate of spread, and competitive stature. Pages 69–80 in Brock, JH, Wade, M, Pyšek, P, Green, D, eds., Plant Invasions: Studies from North America and Europe. Leiden, Netherlands: Backhuys Google Scholar
Braun, EL (1961) The Woody Plants of Ohio. Columbus: Ohio State University Press. 362 pGoogle Scholar
Bunker, DE, DeClerck, F, Bradford, JC, Colwell, RR, Perfecto, I, Phillips, OL, Sankaran, M, Naeem, S (2005) Species loss and aboveground storage in a tropical forest. Science 310:1029–1031 CrossRefGoogle Scholar
Cipollini, D, Dorning, M (2008) Direct and indirect effects of conditioned soils and tissue extracts of the invasive shrub, Lonicera maackii, on target plant performance. Castanea 73:166–176 Google Scholar
Cipollini, D, Titus, K, Wagner, C (2012) Allelopathic effects of invasive species (Alliaria petiolata, Lonicera maackii, Ranunculus ficaria) in the Midwestern United States. Allelopathy J 29:63–76 Google Scholar
Collier, MH, Vankat, JL, Hughes, MR (2002) Diminished plant richness and abundance below Lonicera maackii, an invasive shrub. Am Midl Nat 147:60–71 Google Scholar
Crooks, JA 2005. Lag times and exotic species: the ecology and management of biological invasions in slow-motion. Ecoscience 12:316–329 Google Scholar
De Deyn, GB, Cornelissen, JHC, Bardgett, RD (2008) Plant functional traits and soil carbon sequestration in contrasting biomes. Ecol Lett 11:516–531 Google Scholar
Dorning, M, Cipollini, D (2006) Leaf and root extracts of the invasive shrub, Lonicera maackii, inhibit germination of three herbs with no autotoxic effects. Plant Ecol 184:287–296 Google Scholar
Ehrenfeld, JG (2003) Effects of exotic plant invasions on soil nutrient cycling processes. Ecosystems 6:503–523 Google Scholar
Ehrenfeld, JG (2010) Ecosystem consequences of biological invasions. Annu Rev Ecol Evol Syst 41:59–80 Google Scholar
Ehrenfeld, JG, Kourtev, P, Huang, W (2001) Changes in soil functions following invasions of exotic understory plants in deciduous forests. Ecol Appl 11:1287–1300 CrossRefGoogle Scholar
Evans, RD, Rimer, R, Sperry, L, Belnap, J (2001) Exotic plant invasion alters nitrogen dynamics in an arid grassland. Ecol Appl 11:1301–1310 Google Scholar
Fridley, JD (2012) Extended leaf phenology and the autumn niche in deciduous forest invasions. Nature 485:359–362 Google Scholar
Gaertner, M, Den Breeyen, A, Hui, C, Richardson, DM (2009) Impacts of alien plant invasions on species richness in Mediterranean-type ecosystems: a meta-analysis. Prog Phys Geog 33:319–338 CrossRefGoogle Scholar
Gorchov, DL, Trisel, DE (2003) Competitive effects of the invasive shrub, Lonicera maackii (Rupr.) Herder (Caprifoliaceae), on the growth and survival of native tree seedlings. Plant Ecol 166:13–24 Google Scholar
Grime, JP (1998) Benefits of plant diversity on ecosystems: intermediate, filter, and founder effects. J Ecol 86:902–910 Google Scholar
Grout, JA, Levings, CD, Richardson, JS (1997) Decomposition rates of purple loosestrife (Lythrum salicaria) and Lyngbyei's sedge (Carex lyngbyei) in the Fraser River estuary. Estuar Coast 20:96–102 Google Scholar
Hartman, KM, McCarthy, BC (2004) Restoration of a forest understory after removal of an invasive shrub, Amur honeysuckle (Lonicera maackii). Restor Ecol 12:154–165 Google Scholar
Hartman, KM, McCarthy, BC (2008) Changes in forest structure and species composition following invasion by a non-indigenous shrub, Amur honeysuckle (Lonicera maackii). J Torrey Bot Soc 135:245–259 Google Scholar
Hättenschwiler, S, Tiunov, AV, Scheu, S (2005) Biodiversity and litter decomposition in terrestrial ecosystems. Ann Rev Ecol Evol Syst 36:191–218 CrossRefGoogle Scholar
Hawkes, CV, Wren, IF, Herman, DJ, Firestone, MK (2005) Plant invasion alters nitrogen cycling by modifying the soil nitrifying community. Ecol Lett 8:976–985 Google Scholar
Hutchinson, TF, Vankat, JL (1997) Invasibility and effects of Amur honeysuckle in southwestern Ohio forests. Conserv Biol 11:1117–1124 Google Scholar
Iannone, DC III, Heneghan, L, Rijal, DW, Wise, DH 2015 Below-ground causes and consequences of woodland shrub invasions: a novel paired-point framework reveals new insights. J Appl Ecol 52:78–88 Google Scholar
Knops, JMH, Bradley, KL, Wedin, DA (2002) Mechanisms of plant species impacts on ecosystem nitrogen cycling. Ecol Lett 5:454–466 Google Scholar
Kuebbing, SE, Classen, AT, Call, JJ, Henning, JA, Simberloff, D (2015) Plant–soil interactions promote co-occurrence of three nonnative woody shrubs. Ecology 96:2289–2299 Google Scholar
Kuebbing, SE, Classen, AT, Simberloff, D (2014) Two co-occurring invasive woody shrubs alter soil properties and promote subdominant invasive species. J Appl Ecol 51:124–133 Google Scholar
Lett, MS, Knapp, AK, Briggs, JM, Blair, JM (2004) Influence of shrub encroachment on aboveground net primary productivity and carbon and nitrogen pools in a mesic grassland. Can J Bot 82:1363–1370 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 177:706–714 Google Scholar
Luken, JO (1988) Population structure and biomass allocation of the naturalized shrub Lonicera maackii (Rupr.) Maxim. in forest and open habitats. Am Midl Nat 119:258–267 Google Scholar
Luken, JO, Mattimiro, DT (1991) Habitat-specific resilience of the invasive shrub Amur honeysuckle (Lonicera maackii) during repeated clipping. Ecol Appl 1:104–109 Google Scholar
Luken, JO, Thieret, JW (1996) Amur honeysuckle, its fall from grace. BioScience 46:18–24 CrossRefGoogle Scholar
Luken, JO, Tholemeier, TC, Kunkel, BA, Kuddes, LM (1995) Branch architecture plasticity of Amur honeysuckle (Lonicera maackii (Rupr.) Herder): initial response in extreme light environments. Bull Torrey Bot Club 122:190–195 Google Scholar
Luo, Y, Hui, D, Zhang, D (2006) Elevated CO2 stimulates net accumulations of carbon and nitrogen in land ecosystems: a meta-analysis. Ecology 87:53–63 Google Scholar
McEwan, RW, Arthur, MA, Alverson, SE (2012) Throughfall chemistry and soil nutrient effects of the invasive shrub Lonicera maackii in deciduous forests. Am Midl Nat 168:43–55 Google Scholar
McEwan, RW, Birchfield, MK, Schoergendorfer, A, Arthur, MA (2009) Leaf phenology and freeze tolerance of the invasive shrub Amur honeysuckle and potential native competitors. J Torrey Bot Soc 136:212–220 Google Scholar
Miller, KE, Gorchov, DL (2004) The invasive shrub, Lonicera maackii, reduces growth and fecundity of perennial forest herbs. Oecologia 139:359–375 Google Scholar
Peltzer, DA, Allen, RB, Lovett, GM, Whitehead, D, Wardle, DA (2010) Effects of biological invasion on forest carbon sequestration. Glob Change Biol 16:732–746 CrossRefGoogle Scholar
Post, WM, Emanuel, WR, Zinke, PJ, Stangenberger, AG (1982) Soil carbon pools and world life zones. Nature 298:156–159 CrossRefGoogle Scholar
Poulette, MM, Arthur, MA (2012) The impact of the invasive shrub Lonicera maackii on the decomposition dynamics of a native plant community. Ecol Appl 22:412–424 Google Scholar
Pyšek, P, Jaroški, V., Hulme, PE, Pergl, J, Hejda, M, Schaller, U, Vilá, M (2012) A global assessment of invasive plant impacts on resident species, communities and ecosystems: the interaction of impact measures, invading species’ traits and environment. Glob Change Biol 18:1725–1737 Google Scholar
Raciti, SM, Groffman, PM, Jenkins, JC, Pouyat, RV, Fahey, TJ, Pickett, STA, Cadenasso, ML (2011) Accumulation of carbon and nitrogen in residential soils with different land-use histories. Ecosystems 14:287–297 Google Scholar
Rejmánek, M (2014) Invasive trees and shrubs: where do they come from and what we should expect in the future? Biol Invasions 16:483–498 CrossRefGoogle Scholar
Richardson, DM, Rejmánek, M (2011) Trees and shrubs as invasive alien species—a global review. Divers Distrib 17:788–809 Google Scholar
Schradin, D, Cipollini, D (2012). The sign and strength of plant–soil feedback for the invasive shrub, Lonicera maackii, varies in different soils. Forests 3:903–922 Google Scholar
Scott, NA, Saggar, S, McIntosh, PD (2001) Biochemical impact of Hieracium invasion in New Zealand's grazed tussock grasslands: sustainability implications. Ecol Appl 11:1311–1332 Google Scholar
Shannon, SM., Bauer, JT, Anderson, WE, Reynolds, HL (2014) Plant–soil feedbacks between invasive shrubs and native forest understory species lead to shifts in the abundance of mycorrhizal fungi. Plant Soil 382:317–328 Google Scholar
Simberloff, D (2011) How common are invasion-induced ecosystem impacts? Biol Invasions 13:1255–1268 CrossRefGoogle Scholar
Sitch, S, Smith, B, Prentice, IC, Arneth, A, Bondeau, A, Cramer, W, Kaplan, JO, Levis, S, Lucht, W, Sykes, MT, Thonicke, K, Venevski, S (2003) Evaluation of ecosystem dynamics, plant geography and terrestrial carbon cycling in LPJ dynamic global vegetation model. Glob Change Biol 9:161–185 Google Scholar
Soil Survey Staff, Natural Resources Conservation Service, United States Department of Agriculture, Web Survey. http://websoilsurvey.nrcs.usda.gov/. Accessed January 15, 2011Google Scholar
Stradling, D (2011) Mt. Airy Forest: one hundred years of conservation in the city. Ohio Valley Hist 11:25–43 Google Scholar
Stratton, GW, Stewart, KE (1991) Effects of the herbicide glyphosate on nitrogen cycling in an acid forest soil. Water Air Soil Poll 60:231–247 CrossRefGoogle Scholar
Strayer, DL, Eviner, VT, Jeschke, JM, Pace, ML (2006) Understanding the long-term effects of species invasions. Trends Ecol Evol 21:645–651 Google Scholar
Trammell, TLE, Carreiro, MM (2011) Vegetation composition and structure of woody plant communities along urban interstate corridors in Louisville, KY, U.S.A. Urban Ecosyst 14:501–524 Google Scholar
Trammell, TLE, Ralston, HA, Scroggins, SA, Carreiro, MM (2012) Foliar production and decomposition rates in urban forests invaded by the exotic invasive shrub, Lonicera maackii . Biol Invasions 14:529–545 CrossRefGoogle Scholar
Trammell, TLE, Schneid, BP, Carreiro, MM (2011) Forest soils adjacent to urban interstates: soil physical and chemical properties, heavy metals, disturbance legacies, and relationships with woody vegetation. Urban Ecosyst 14:525–552 Google Scholar
Townsend-Small, A, Czimczik, CI (2010) Carbon sequestration and greenhouse gas emissions in urban turf. Geophys Res Lett 37: L02707. DOI: 10.1029/2009GL041675Google Scholar
[USDA NRCS] U.S. Department of Agriculture Natural Resources Conservation Service (2014) The PLANTS Database. http://plants.usda.gov. Accessed October 31, 2014Google Scholar
van der Heijden, MGA, Bardgett, RD, van Straalen, NM (2008) The unseen majority: soil microbes as drivers of plant diversity and productivity in terrestrial ecosystems. Ecol Lett 11:296–310 CrossRefGoogle ScholarPubMed
Vilà, M, Espinar, JL, Hejda, M, Hume, PE, Jaroŝík, V, Maron, JL, Pergl, J, Schaffnew, U, Sun, Y, Pyŝek, P (2011) Ecological impacts of invasive alien plants: a meta-analysis of their effects on species, communities, and ecosystems. Ecol Lett 14:702–708 Google Scholar
Vitousek, PM, D’Antonio, CM, Loope, LL, Rejmanek, M, Westbrooks, RZ (1997) Introduced species: a significant component of human-caused global change. N Z J Ecol 21:1–16 Google Scholar
Vitousek, PM, Walker, LR (1989) Biological invasion by Myrica faya in Hawai'i: plant demography, nitrogen fixation, ecosystem effects. Ecol Monogr 59:247–265 Google Scholar
Watson, ME, Brown, JR (1998) pH and lime requirement. Pages 13–16 in North Central Regional Res Pub 221:13-1688. Wageningen, Netherlands: International Institute for Land Reclamation and Improvement Google Scholar
Weidenhamer, JD, Callaway, RM (2010) Direct and indirect effects of invasive plants on soil chemistry and ecosystem function. J Chem Ecol 36:59–69 Google Scholar
Windam, L, Ehrenfeld, JG (2003) Net impact of a plant invasion on nitrogen-cycling processes within a brackish tidal marsh. Ecol Appl 13:883–897 CrossRefGoogle Scholar