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Insect herbivore effects on resource allocation to shoots and roots in Lespedeza capitata

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Abstract

Aboveground and belowground processes in plants are intimately linked because the resources that must be divided among growth, maintenance, and development of essential structures are finite. To determine how aboveground insect herbivory affects root-system size, morphology, interactions with soil biota, and temporal patterns in the development of root systems, we grew the legume Lespedeza capitata in sunken pots in a restored prairie in south-central Kansas. The plants were manipulated in a factorial experiment that involved reduction of natural herbivory with insecticide and age of plant at harvest (2, 4, or 6 months). Herbivory reduced the aboveground sizes of plants throughout the growing season but did not affect their belowground size or root-system branching ratio. Further, the failure of aboveground insect herbivory to affect density of nitrogen-fixing nodules on L. capitata roots suggests that plants did not shift allocation of carbon to compensate for naturally occurring levels of folivory. We suggest that conservation of root-system structure or low rates of change in root-system structure in response to aboveground insect herbivory may be an adaptive strategy in environments with scarce soil resources, for example near species’ xeric range limits.

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References

  • Amsberry LK, Maron JL (2006) Effects of herbivore identity on plant fecundity. Plant Ecol 187:39–48

    Article  Google Scholar 

  • Ayres E, Dromph KM, Cook R, Ostle N, Bardgett RD (2007) The influence of below-ground herbivory and defoliation of a legume on nitrogen transfer to neighbouring plants. Funct Ecol 21:256–263

    Article  Google Scholar 

  • Bardgett RD, Wardle DA (2010) Aboveground-belowground linkages: biotic interactions, ecosystem processes and global change. Oxford University Press, Oxford

    Google Scholar 

  • Bardgett RD, Wardle DA, Yeates GW (1998) Linking above-ground and below-ground interactions: how plant responses to foliar herbivory influence soil organisms. Soil Biol Biochem 30:1867–1878

    Article  CAS  Google Scholar 

  • Cain ML, Carson WP, Root RB (1991) Long-term suppression of insect herbivores increases the production and growth of Solidago altissima rhizomes. Oecologia 88:251–257

    Article  Google Scholar 

  • Callaway RM, DeLuca TH, Belliveau WM (1999) Biological-control herbivores may increase competitive ability of the noxious weed Centaurea maculosa. Ecology 80:1196–1201

    Google Scholar 

  • Chapin F III, Bloom A, Field C, Waring R (1987) Plant response to multiple environmental factors. Bioscience 37:49–57

    Article  Google Scholar 

  • Clark KE, Hartley SE, Johnson SN (2011) Does mother know best? The preference-performance hypothesis and parent-offspring conflict in aboveground-belowground herbivore life cycles. Ecol Entomol 36:117–124

    Article  Google Scholar 

  • Crawley MJ (1989) The relative importance of vertebrate and invertebrate herbivores in plant population dynamics. In: Bernays EA (ed) Insect-plant interactions. CRC Press, Boca Raton, pp 45–71

    Google Scholar 

  • Cripps MG, Edwards GR, Bourdot GW, Saville DJ, Hinz HL, Fowler SV (2010) Effects of pasture competition and specialist herbivory on the performance of Cirsium arvense. Biocontrol Sci Technol 20:641–656

    Article  Google Scholar 

  • Eyles A, Pinkard EA, Mohammad C (2009) Shifts in biomass and resource allocation patterns following defoliation in Eucalyptus globulus growing with varying water and nutrient supplies. Tree Phys 29:753–764

    Article  CAS  Google Scholar 

  • Fitter AH (1982) Morphometric analysis of root systems: application of the technique and influence of soil fertility on root system development in two herbaceous species. Plant, Cell Environ 5:313–322

    Google Scholar 

  • Gassmann AJ (2004) Effects of photosynthetic efficiency and water availability on tolerance of leaf removal in Amaranthus hybridus. J Ecol 92:882–892

    Article  CAS  Google Scholar 

  • Gehring CA, Whitham TG (2002) Mycorrhizae-herbivore interactions: population and community consequences. In: van der Heijden MGA, Sanders LR (eds) Mycorrhizal ecology. Springer, Berlin, pp 295–320

    Google Scholar 

  • Great Plains Flora Association (1986) Flora of the great plains. University Press of Kansas, Lawrence

    Google Scholar 

  • Gregory PJ (2006) Plant roots: growth, activity and interactions with soils. Blackwell Publishing, Oxford

    Google Scholar 

  • Hochwender CG, Marquis RJ, Stowe KA (2000) The potential for and constraints on the evolution of compensatory ability in Asclepias syriaca. Oecologia 122:361–370

    Article  Google Scholar 

  • Hochwender CG, Cha DH, Czesk ME, Fritz RS, Smyth RR, Kaufman AD, Warren B, Neuman, A (2011) Protein storage and root:shoot reallocation provide tolerance to damage in a hybrid willow system. Oecologia. doi:10.1007/s00442-011-2176-9

  • Hol WHG, Macel M, van Veen JA, van der Meijden E (2004) Root damage and aboveground herbivory change concentration and composition pyrrolizidine alkaloids in Senecio jacobaea. Basic Appl Ecol 5:253–260

    Article  CAS  Google Scholar 

  • Holland EA, Detling JK (1990) Plant response to herbivory and belowground nitrogen cycling. Ecology 71:1040–1049

    Article  Google Scholar 

  • Holland JN, Cheng W, Crossley DA (1996) Herbivore-induced changes in plant carbon allocation: assessment of belowground C-fluxes using carbon-14. Oecologia 107:87–94

    Article  Google Scholar 

  • Johnson SN, Bezemer TM, Jones TH (2008) Linking aboveground and belowground herbivory. In: Johnson SN, Murray PJ (eds) Root feeders: an ecosystem perspective. CAB International, Wallingford, pp 153–170

    Chapter  Google Scholar 

  • Kadiata BD, Mulongoy K, Mambani B (1998) Pruning effect on nitrogen release in the root zone of Albizia lebbeck and Leucaena leucocephala. Biol Fert Soils 26:187–193

    Article  CAS  Google Scholar 

  • Kula AAR, Hartnett DC, Wilson GWT (2005) Effects of mycorrhizal symbiosis on tallgrass prairie plant-herbivore interactions. Ecol Lett 8:61–69

    Article  Google Scholar 

  • Ludwig-Müller J, Schubert B, Pieper K, Ihmig S, Hilgenberg W (1997) Glucosinolate content in susceptible and resistant Chinese cabbage varieties during development of clubroot disease. Phytochem 44:407–414

    Article  Google Scholar 

  • Meyer GA (2000) Interactive effects of soil fertility and herbivory on Brassica nigra. Oikos 88:433–441

    Article  Google Scholar 

  • Mikola J, Setala H, Virkajarvi P, Saarijarvi K, Voigt W, Vestberg M (2009) Defoliation and patchy nutrient return drive grazing effects on plant and soil properties in a dairy cow pasture. Ecol Monogr 79:221–244

    Article  Google Scholar 

  • Moran NA, Whitham TG (1990) Interspecific competition between root-feeding and leaf-galling aphids mediated by host plant resistance. Ecology 71:1050–1058

    Article  Google Scholar 

  • Quezada IM, Gianoli E (2010) Counteractive biomass allocation responses to drought and damage in the perennial herb Convolvulus demissus. Austral Ecol 35:544–548

    Article  Google Scholar 

  • Quinn MA, Hall MH (1996) Compensatory growth response of the legume, Medicago sativa, to defoliation and denodulation. Entomol Exp Appl 78:243–252

    Article  Google Scholar 

  • R Development Core Team (2009) R: a language and environment for statistical computing. R Foundation for Statistical Computing, Vienna. ISBN 3-900051-07-0. http://www.R-project.org

  • Rausher MD, Feeny P (1980) Herbivory, plant density and plant reproductive success: the effect of Battus philenor on Aristolochia reticulata. Ecology 61:905–917

    Article  Google Scholar 

  • Rudgers JA, Hoeksema JD (2003) Inter-annual variation in above- and belowground herbivory on a native, annual legume. Plant Ecol 169:105–120

    Article  Google Scholar 

  • Russell FL, Rose KE, Louda SM (2010) Seed availability and insect herbivory limit recruitment and adult density of native tall thistle. Ecology 91:3081–3093

    Article  PubMed  Google Scholar 

  • Schwachtje J, Minchin PEH, Jahnke S, van Dongen JT, Schittko U, Baldwin IT (2006) SNF-1 related kinases allow plants to tolerate herbivory by allocating carbon to roots. Proc Natl Acad Sci USA 103:12935–12940

    Article  PubMed  CAS  Google Scholar 

  • Sessions LA, Kelly D (2001) Heterogeneity in vertebrate and invertebrate herbivory and its consequences for New Zealand mistletoes. Austral Ecol 26:571–581

    Article  Google Scholar 

  • Soler R, Bezemer TM, Cortesero AM, van der Putten WM, Vet LEM, Harvey JA (2007) Impact of foliar herbivory on the development of a root-feeding insect and its parasitoid. Oecologia 152:257–264

    Article  PubMed  Google Scholar 

  • Spehn EM, Scherer-Lorenzen M, Schmid B, Hector A, Caldeira MC, Dimitrikopoulus PG, Finn JA, Jumpponen A, O’Donovan G, Pereira JS, Schulze ED, Troumbis AY, Korner C (2002) The role of legumes as a component of biodiversity in a cross-European study of grassland biomass nitrogen. Oikos 98:205–218

    Article  Google Scholar 

  • Stowe KA, Marquis RJ, Hochwender CG, Simms EL (2000) The evolutionary ecology of tolerance to consumer damage. Annu Rev Ecol Syst 31:565–595

    Article  Google Scholar 

  • Strauss SY, Agrawal AA (1999) The ecology and evolution of plant tolerance to herbivory. Trends Ecol Evol 44:179–185

    Article  Google Scholar 

  • Strauss SY, Watson W, Allen MT (2003) Predictors of male and female tolerance to insect herbivory in Raphanus raphanistrum. Ecology 84:2074–2082

    Article  Google Scholar 

  • United States Department of Agriculture (1979) Soil survey of Sedgwick County, Kansas. United States Department of Agriculture, Washington

    Google Scholar 

  • United States Department of Agriculture (2011) The PLANTS database. National Plant Data Team, Greensboro. http://plants.usda.gov. 27 Sept 2011

  • Weaver JE, Fitzpatrick TJ (1934) The prairie. Ecol Monogr 4:190–295

    Article  Google Scholar 

Download references

Acknowledgments

We thank Wichita State University for the use of the Ninnescah Reserve and the renovated Hubbard Hall greenhouse. We thank T. E. Miller, A. L. Buchanan, D. W. McNutt, E. S. Gornish, and N. A. Kortessis, as well as two anonymous reviewers whose comments greatly improved the manuscript. D. Cork, B. Wells, B. Stuckey, M. Cork, and K. Cook provided invaluable help with field work. This is contribution #20 of the WSU Biological Field Station.

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Correspondence to Abigail I. Pastore.

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Pastore, A.I., Russell, F.L. Insect herbivore effects on resource allocation to shoots and roots in Lespedeza capitata . Plant Ecol 213, 843–851 (2012). https://doi.org/10.1007/s11258-012-0046-0

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