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CHAPTER ELEVEN - Impacts of climate change on trophic interactions in grasslands

from Part II - Species traits, functional groups, and evolutionary change

Published online by Cambridge University Press:  22 March 2019

David J. Gibson
Affiliation:
Southern Illinois University, Carbondale
Jonathan A. Newman
Affiliation:
University of Guelph, Ontario
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Publisher: Cambridge University Press
Print publication year: 2019

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References

11.7 References

Sala, OE, Vivanco, L, Flombaum, P. Grassland ecology. In: Encyclopedia of biodiversity [Internet]. 2nd edn.; Burlington, USA: Elsevier Science. 2013. pp. 17.Google Scholar
O’Mara, FP. The role of grasslands in food security and climate change. Annals of Botany. 2012;110(6):1263–70.Google Scholar
Suttle, KB, Thomsen, MA, Power, ME. Species interactions reverse grassland responses to changing climate. Science. 2007;315(5812):640–2.Google Scholar
Craine, JM, Elmore, AJ, Olson, K, Tolleson, D. Climate change and cattle nutritional stress. Global Change Biology. 2010;16(10):2901–11.Google Scholar
Robinson, EA, Ryan, GD, Newman, JA. A meta‐analytical review of the effects of elevated CO2 on plant–arthropod interactions highlights the importance of interacting environmental and biological variables. New Phytologist. 2012;194(2):321–36.Google Scholar
Terborgh, J, Estes, JA. Trophic cascades: predators, prey, and the changing dynamics of nature. Washington, DC: Island Press; 2013.Google Scholar
Wand, SJE, Midgley, G, Jones, MH, Curtis, PS. Responses of wild C4 and C3 grass (Poaceae) species to elevated atmospheric CO2 concentration: a meta‐analytic test of current theories and perceptions. Global Change Biology. 1999;5(6):723–41.Google Scholar
Tyliaakis, JM, Didham, RK, Bascompte, J, Wardle, DA. Global change and species interactions in terrestrial ecosystems. Ecology Letters. 2008;11(12):1351–63.Google Scholar
Zvereva, EL, Kozlov, MV. Consequences of simultaneous elevation of carbon dioxide and temperature for plant–herbivore interactions: a meta-analysis. Global Change Biology. 2006;12(1):2741.Google Scholar
Johnson, SN, Hartley, SE. Elevated carbon dioxide and warming impact silicon and phenolic‐based defences differently in native and exotic grasses. Global Change Biology. 2017.Google Scholar
Gherardi, LA, Sala, OE. Enhanced interannual precipitation variability increases plant functional diversity that in turn ameliorates negative impact on productivity. Ecology Letters. 2015;18(12):1293–300.Google Scholar
IPCC. Climate change 2013: the physical science basis. Contribution of Working Group I to the Fifth Assessment Report of the Intergovernmental Panel on Climate Change. Stocker, TF, Qin, D, Plattner, G-K, Tignor, M, Allen, SK, Boschung, J, et al., editors. Cambridge: Cambridge University Press; 2013. 1535 pp.Google Scholar
Stireman, J, Dyer, LA, Janzen, DH, Singer, M, Lill, J, Marquis, RJ, et al. Climatic unpredictability and parasitism of caterpillars: implications of global warming. Proceedings of the National Academy of Sciences of the USA. 2005;102(48):17,384–7.Google Scholar
Jones, CG, Hartley, SE. A protein competition model of phenolic allocation. Oikos. 1999;86(1):2744.Google Scholar
Bezemer, TM, Jones, TH. Plant–insect herbivore interactions in elevated atmospheric CO2: quantitative analyses and guild effects. Oikos. 1998;82:212–22.Google Scholar
Stiling, P, Cornelissen, T. How does elevated carbon dioxide (CO2) affect plant–herbivore interactions? A field experiment and meta‐analysis of CO2‐mediated changes on plant chemistry and herbivore performance. Global Change Biology. 2007;13(9):1823–42.Google Scholar
Luo, Y, Hui, D, Zhang, D. Elevated CO2 stimulates net accumulations of carbon and nitrogen in land ecosystems: a meta‐analysis. Ecology. 2006;87(1):5363.Google Scholar
Gargallo‐Garriga, A, Sardans, J, Pérez‐Trujillo, M, Oravec, M, Urban, O, Jentsch, A, et al. Warming differentially influences the effects of drought on stoichiometry and metabolomics in shoots and roots. New Phytologist. 2015;207(3):591603.Google Scholar
Johnson, SN, Lopaticki, G, Hartley, SE. Elevated atmospheric CO2 triggers compensatory feeding by root herbivores on a C3 but not a C4 grass. PloS ONE. 2014;9(3):e90251.Google Scholar
Morgan, JA, LeCain, DR, Pendall, E, Blumenthal, DM, Kimball, BA, Carrillo, Y, et al. C4 grasses prosper as carbon dioxide eliminates desiccation in warmed semi-arid grassland. Nature. 2011;476(7359):202.Google Scholar
Zavaleta, ES, Shaw, MR, Chiariello, NR, Thomas, BD, Cleland, EE, Field, CB, et al. Grassland responses to three years of elevated temperature, CO2, precipitation, and N deposition. Ecological Monographs. 2003;73(4):585604.Google Scholar
Hartley, SE, Jones, CG, Couper, GC, Jones, TH. Biosynthesis of plant phenolic compounds in elevated atmospheric CO2. Global Change Biology. 2000;6(5):497506.Google Scholar
Reich, PB, Hobbie, SE, Lee, TD. Plant growth enhancement by elevated CO2 eliminated by joint water and nitrogen limitation. Nature Geoscience. 2014;7(12):920.Google Scholar
Hartley, SE, DeGabriel, JL. The ecology of herbivore‐induced silicon defences in grasses. Functional Ecology. 2016;30(8):1311–22.CrossRefGoogle Scholar
Ryalls, JM, Hartley, SE, Johnson, SN. Impacts of silicon-based grass defences across trophic levels under both current and future atmospheric CO2 scenarios. Biology Letters. 2017;13(3):20160912.Google Scholar
McLarnon, E, McQueen-Mason, S, Lenk, I, Hartley, SE. Evidence for active uptake and deposition of Si-based defenses in tall fescue. Frontiers in Plant Science. 2017;8:1199.Google Scholar
Buitenwerf, R, Bond, W, Stevens, N, Trollope, W. Increased tree densities in South African savannas: > 50 years of data suggests CO2 as a driver. Global Change Biology. 2012;18(2):675–84.Google Scholar
Cui, T, Martz, L, Guo, X. Grassland phenology response to drought in the Canadian Prairies. Remote Sensing. 2017;9(12):1258.Google Scholar
Harris, G, Thirgood, S, Hopcraft, JGC, Cromsight, JPGM, Berger, J. Global decline in aggregated migrations of large terrestrial mammals. Endangered Species Research. 2009;7:5576.Google Scholar
DeLucia, EH, Nabity, PD, Zavala, JA, Berenbaum, MR. Climate change: resetting plant–insect interactions. Plant Physiology. 2012;160(4):1677–85.Google Scholar
AbdElgawad, H, Peshev, D, Zinta, G, Van den Ende, W, Janssens, IA, Asard, H. Climate extreme effects on the chemical composition of temperate grassland species under ambient and elevated CO2: a comparison of fructan and non-fructan accumulators. PLoS ONE. 2014;9(3):e92044.Google Scholar
Massey, FP, Massey, K, Ennos, AR, Hartley, SE. Impacts of silica-based defences in grasses on the feeding preferences of sheep. Basic and Applied Ecology. 2009;10(7):622–30.Google Scholar
Reynolds, OL, Keeping, MG, Meyer, JH. Silicon‐augmented resistance of plants to herbivorous insects: a review. Annals of Applied Biology. 2009;155(2):171–86.Google Scholar
Wade, RN, Karley, AJ, Johnson, SN, Hartley, SE. Impact of predicted precipitation scenarios on multitrophic interactions. Functional Ecology. 2017;31(8):1647–58.Google Scholar
Flannigan, MD, Krawchuk, MA, de Groot, WJ, Wotton, BM, Gowman, LM. Implications of changing climate for global wildland fire. International Journal of Wildland Fire. 2009;18(5):483507.Google Scholar
Jolly, WM, Cochrane, MA, Freeborn, PH, Holden, ZA, Brown, TJ, Williamson, GJ, et al. Climate-induced variations in global wildfire danger from 1979 to 2013. Nature Communications. 2015;6:7537.Google Scholar
Bond, WJ, Keeley, JE. Fire as a global ‘herbivore’: the ecology and evolution of flammable ecosystems. Trends in Ecology & Evolution. 2005;20(7):387–94.Google Scholar
Alstad, AO, Damschen, EI, Givnish, TJ, Harrington, JA, Leach, MK, Rogers, DA, et al. The pace of plant community change is accelerating in remnant prairies. Science Advances. 2016;2(2):e1500975.Google Scholar
Archibald, S. Managing the human component of fire regimes: lessons from Africa. Philosophical Transactions of the Royal Society B: Biological Sciences. 2016;371(1696):20150346.Google Scholar
Hempson, GP, Parr, CL, Archibald, S, Anderson, TM, Mustaphi, CJC, Dobson, AP, et al. Continent‐level drivers of African pyrodiversity. Ecography. 2018;41(6):889–99.Google Scholar
Ojima, DS, Schimel, D, Parton, W, Owensby, C. Long- and short-term effects of fire on nitrogen cycling in tallgrass prairie. Biogeochemistry. 1994;24(2):6784.Google Scholar
Van de Vijver, CADM, Poot, P, Prins, HHT. Causes of increased nutrient concentrations in post-fire regrowth in an East African savanna. Plant and Soil. 1999;214(1–2):173–85.Google Scholar
Byenkya, GS, Gumisiriza, G, Kasigwa, H. Evaluation of control strategies for Cymbopogon nardus in grazing areas of Uganda. Journal of Agricultural Science and Technology. 2013;3(9B):656.Google Scholar
Bale, JS, Masters, GJ, Hodkinson, ID, Awmack, C, Bezemer, TM, Brown, VK, et al. Herbivory in global climate change research: direct effects of rising temperature on insect herbivores. Global Change Biology. 2002;8(1):116.Google Scholar
Awmack, CS, Leather, SR. Host plant quality and fecundity in herbivorous insects. Annual Review of Entomology. 2002;47(1):817–44.Google Scholar
Nord, EA, Lynch, JP. Plant phenology: a critical controller of soil resource acquisition. Journal of Experimental Botany. 2009;60(7):1927–37.Google Scholar
Mattson, WJ, Haack, RA. The role of drought in outbreaks of plant-eating insects. Bioscience. 1987;37(2):110–8.Google Scholar
de Sassi, C, Tylianakis, JM. Climate change disproportionately increases herbivore over plant or parasitoid biomass. PLoS ONE. 2012;7(7):e40557.Google Scholar
Yu, G, Shen, H, Liu, J. Impacts of climate change on historical locust outbreaks in China. Journal of Geophysical Research: Atmospheres. 2009;114(D18).Google Scholar
Johnson, SN, Staley, JT, McLeod, FA, Hartley, SE. Plant‐mediated effects of soil invertebrates and summer drought on above‐ground multitrophic interactions. Journal of Ecology. 2011;99(1):5765.Google Scholar
Pritchard, J, Griffiths, B, Hunt, E. Can the plant‐mediated impacts on aphids of elevated CO2 and drought be predicted? Global Change Biology. 2007;13(8):1616–29.Google Scholar
Hopcraft, JGC, Anderson, TM, Pérez‐Vila, S, Mayemba, E, Olff, H. Body size and the division of niche space: food and predation differentially shape the distribution of Serengeti grazers. Journal of Animal Ecology. 2012;81(1):201–13.Google Scholar
Hopcraft, JGC, Olff, H, Sinclair, A. Herbivores, resources and risks: alternating regulation along primary environmental gradients in savannas. Trends in Ecology & Evolution. 2010;25(2):119–28.Google Scholar
McNaughton, SJ. Grazing lawns: animals in herds, plant form, and coevolution. The American Naturalist. 1984;124:863–86.Google Scholar
Archibald, S. African grazing lawns – how fire, rainfall, and grazer numbers interact to affect grass community states. Journal of Wildlife Management. 2008;72(2):492501.Google Scholar
Donaldson, JE, Archibald, S, Govender, N, Pollard, D, Luhdo, Z, Parr, CL. Ecological engineering through fire–herbivory feedbacks drives the formation of savanna grazing lawns. Journal of Applied Ecology. 2018;55(1):225–35.Google Scholar
Ogutu, JO, Piepho, H-P, Dublin, HT. Reproductive seasonality in African ungulates in relation to rainfall. Wildlife Research. 2015;41(4):323–42.Google Scholar
Langvatn, R, Mysterud, A, Stenseth, NC, Yoccoz, NG. Timing and synchrony of ovulation in red deer constrained by short northern summers. The American Naturalist. 2004;163(5):763–72.Google Scholar
Mduma, SA, Sinclair, A, Hilborn, R. Food regulates the Serengeti wildebeest: a 40‐year record. Journal of Animal Ecology. 1999;68(6):1101–22.Google Scholar
Post, E, Pedersen, C. Opposing plant community responses to warming with and without herbivores. Proceedings of the National Academy of Sciences of the USA. 2008;105(34):12,353–8.Google Scholar
Hartley, SE, Gange, AC. Impacts of plant symbiotic fungi on insect herbivores: mutualism in a multitrophic context. Annual Review of Entomology. 2009;54:323–42.Google Scholar
Brosi, GB, McCulley, RL, Bush, LP, Nelson, JA, Classen, AT, Norby, RJ. Effects of multiple climate change factors on the tall fescue–fungal endophyte symbiosis: infection frequency and tissue chemistry. New Phytologist. 2011;189(3):797805.Google Scholar
Harrington, R, Woiwod, I, Sparks, T. Climate change and trophic interactions. Trends in Ecology & Evolution. 1999;14(4):146–50.Google Scholar
Beale, CM, Baker, NE, Brewer, MJ, Lennon, JJ. Protected area networks and savannah bird biodiversity in the face of climate change and land degradation. Ecology Letters. 2013;16(8):1061–8.Google Scholar
Stenseth, NC, Mysterud, A. Climate, changing phenology, and other life history traits: nonlinearity and match–mismatch to the environment. Proceedings of the National Academy of Sciences of the USA. 2002;99(21):13,379–81.Google Scholar
Woodroffe, R, Groom, R, McNutt, JW. Hot dogs: high ambient temperatures impact reproductive success in a tropical carnivore. Journal of Animal Ecology. 2017;86(6):1329–38.Google Scholar
Loarie, SR, Tambling, CJ, Asner, GP. Lion hunting behaviour and vegetation structure in an African savanna. Animal Behaviour. 2013;85(5):899906.Google Scholar
Riginos, C. Climate and the landscape of fear in an African savanna. Journal of Animal Ecology. 2015;84(1):124–33.Google Scholar
deMenocal, PB. African climate change and faunal evolution during the Pliocene–Pleistocene. Earth and Planetary Science Letters. 2004;220(1–2):324.Google Scholar
Grime, JP, Fridley, JD, Askew, AP, Thompson, K, Hodgson, JG, Bennett, CR. Long-term resistance to simulated climate change in an infertile grassland. Proceedings of the National Academy of Sciences of the USA. 2008;105(29):10,028–32.Google Scholar

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