Biological Invasions

, Volume 12, Issue 6, pp 1685–1694 | Cite as

Physiological responses to short-term water and light stress in native and invasive plant species in southern California

  • Jennifer L. FunkEmail author
  • Virginia A. Zachary
Original Paper


As climate variability increases in low-resource environments, the ability of native and invasive species to tolerate stress and respond to large, ephemeral resource pulses will strongly influence plant fitness and, consequently, competitive outcomes. We examined how native and invasive species occurring in arid coastal sage scrub communities in southern California responded to water and high-light stress. We also examined how plants responded to irrigation following short-term water stress. While species responded differently to water and light treatments, no general pattern emerged between native and invasive species. Photosynthetic function of Ricinus communis (invasive) and Salvia mellifera (native) was most robust to water stress and most responsive to irrigation following water stress. Leaf transpiration data suggested that Ricinus and Salvia maintained photosynthetic function by high water use efficiency rather than higher water status via large root biomass. Brassica nigra (invasive) and Encelia californica (native) were more resistant to photoinhibition in response to high-light stress than Ricinus, Salvia, Artemesia californica (native) or Nicotiana glauca (invasive). Our data suggest that native and invasive species in these arid systems display a range of physiological responses to stress and that strategies for invasive species control or native ecosystem restoration based on plant responses to stress may require species-specific approaches.


Resource availability Water stress Photoinhibition Resource use efficiency Precipitation pulses Plasticity 



We thank Erick Reisinger and Lori Glenwinkel for their assistance in the lab and field. Molly Cavaleri and Christine Creese provided valuable comments that greatly improved the manuscript. This work was supported in part by a grant from the Office of Sponsored Research, Office of the Chancellor, Chapman University.


  1. Ackerly DD, Bazzaz FA (1995) Leaf dynamics, self-shading and carbon gain in seedlings of a tropical pioneer tree. Oecologia 101:289–298CrossRefGoogle Scholar
  2. Barker DH, Vanier C, Naumburg E, Charlet TN, Nielsen KM, Newingham BA, Smith SD (2006) Enhanced monsoon precipitation and nitrogen deposition affect leaf traits and photosynthesis differently in spring and summer in the desert shrub Larrea tridentata. New Phytol 169:799–808CrossRefPubMedGoogle Scholar
  3. Baruch Z, Goldstein G (1999) Leaf construction cost, nutrient concentration, and net CO2 assimilation of native and invasive species in Hawaii. Oecologia 121:183–192CrossRefGoogle Scholar
  4. BassiriRad H, Tremmel DC, Virginia RA, Reynolds JF, de Soyza AG, Brunell MH (1999) Short-term patterns in water and nitrogen acquisition by two desert shrubs following a simulated summer rain. Plant Ecol 145:27–36CrossRefGoogle Scholar
  5. Burns JH, Winn AA (2006) A comparison of plastic responses to competition by invasive and non-invasive congeners in the Commelinaceae. Biol Invasions 8:797–807CrossRefGoogle Scholar
  6. Cavender-Bares J, Bazzaz FA (2004) From leaves to ecosystems: using chlorophyll fluorescence to assess photosynthesis and plant function in ecological studies. In: Papageorgiou GC, Govindjee (eds) Chlorophyll a fluorescence: a signature of photosynthesis. Springer, The Netherlands, pp 737–755Google Scholar
  7. Chapin FS III (1991) Integrated responses of plants to stress. Bioscience 41:29–36CrossRefGoogle Scholar
  8. Chesson P, Gebauer RLE, Schwinning S, Huntly N, Wiegand K, Ernest MSK, Sher A, Novoplansky A, Weltzin JF (2004) Resource pulses, species interactions, and diversity maintenance in arid and semi-arid environments. Oecologia 141:236–253CrossRefPubMedGoogle Scholar
  9. Comar V, Tilley D, Felix E, Turdera M, Chagas Neto M (2004) Comparative energy evaluation of Castor bean (Ricinus communis) production systems in Brazil and the U.S. In: Ortega E, Ulgiati S (eds) Proceedings of IV biennial international workshop “Advances in energy studies”, pp 227–237, Unicamp, Campinas, SP, BrazilGoogle Scholar
  10. Coyle DR, Coleman MD (2005) Forest production responses to irrigation and fertilization are not explained by shifts in allocation. For Ecol Manag 208:137–152CrossRefGoogle Scholar
  11. Davis MA, Grime JP, Thompson K (2000) Fluctuating resources in plant communities: a general theory of invasibility. J Ecol 88:528–534CrossRefGoogle Scholar
  12. Demmig-Adams B, Adams WW III (1992) Photoprotection and other responses of plants to high light stress. Annual Review of Plant Physiology and Plant Molecular Biology 73:599–626CrossRefGoogle Scholar
  13. Diffenbaugh NS, Pal JS, Trapp RJ, Giorgi F (2005) Fine-scale processes regulate the response of extreme events to global climate change. Proceedings of the national academy of science 102: 15774–15778Google Scholar
  14. Durand LZ, Goldstein G (2001) Photosynthesis, photoinhibition, and nitrogen use efficiency in native and invasive tree ferns in Hawaii. Oecologia 126:345–354CrossRefGoogle Scholar
  15. Ehleringer JR, Mooney HA (1978) Effects on physiological activity and adaptive value to a desert shrub. Oecologia 37:183–200CrossRefGoogle Scholar
  16. Ennahli S, Earl HJ (2005) Physiological limitations to photosynthetic carbon assimilation in cotton under water stress. Crop Sci 45:2374–2382CrossRefGoogle Scholar
  17. Feng Y, Lei Y-B, Wang Y-P, Callaway RM, Valiente-Banuet A, Inderjit, Li Y-P, Zheng Y-L (2009) Evolutionary tradeoffs for nitrogen allocation to photosynthesis versus cell walls in an invasive plant. Proc Natl Acad Sci 106:1853–1856CrossRefPubMedGoogle Scholar
  18. Funk JL (2008) Differences in plasticity between invasive and native plants from a low resource environment. J Ecol 96:1162–1174CrossRefGoogle Scholar
  19. Funk JL, Vitousek PM (2007) Resource use efficiency and plant invasion in low-resource systems. Nature 446:1079–1081CrossRefPubMedGoogle Scholar
  20. Funk JL, Cleland EE, Suding KN, Zavaleta ES (2008) Restoration through re-assembly: plant traits and invasion resistance. Trends Ecol Evol 23:695–703CrossRefPubMedGoogle Scholar
  21. Gebauer RLE, Ehleringer JR (2000) Water and nitrogen uptake patterns following moisture pulses in a cold desert community. Ecology 81:1415–1424CrossRefGoogle Scholar
  22. Gleason SM, Ares A (2004) Photosynthesis, carbohydrate storage and survival of a native and an introduced species in relation to light and defoliation. Tree Physiol 24:1087–1097PubMedGoogle Scholar
  23. Gotelli NJ, Ellison AM (2004) A primer of ecological statistics. Sinauer Associates Inc., Sunderland, MAGoogle Scholar
  24. Grotkopp E, Rejmanek M, Rost TL (2002) Toward a causal explanation of plant invasiveness: seedling growth and life-history strategies of 29 pine (Pinus) species. Am Nat 159:396–419CrossRefPubMedGoogle Scholar
  25. Hamilton MA, Murray BR, Cadotte MW, Hose GC, Baker AC, Harris CJ, Licari D (2005) Life-history correlates of plant invasiveness at regional and continental scales. Ecol Lett 8:1066–1074CrossRefGoogle Scholar
  26. Hellmers H, Horton JS, Juhren G, O’Keefe J (1955) Root systems of some chaparral plants in southern California. Ecology 36:667–678CrossRefGoogle Scholar
  27. Huxman TE, Cable JM, Ignace DD, Eilts JA, English NB, Weltzin J, Williams DG (2004) Response of net ecosystem gas exchange to a simulated precipitation pulse in a semi-arid grassland: the role of native versus non-native grasses and soil texture. Oecologia 141:295–305PubMedGoogle Scholar
  28. Ignace DD, Huxman TE, Weltzin JF, Williams DG (2007) Leaf gas exchange and water status responses of a native and non-native grass to precipitation across contrasting soil surfaces in the Sonoran Desert. Oecologia 152:401–413CrossRefPubMedGoogle Scholar
  29. James JJ, Richards JH (2005) Plant nitrogen capture from pulses: effects of pulse size, growth rate, and other soil resources. Oecologia 145:113–122CrossRefPubMedGoogle Scholar
  30. Jenerette GD, Scott RL, Huxman TE (2008) Whole ecosystem metabolic pulses following precipitation events. Funct Ecol 22:924–930CrossRefGoogle Scholar
  31. Knapp AK, Beier C, Briske DD, Classen AT, Luo Y, Reichstein M, Smith MD, Smith SE, Bell JE, Fay PA, Heisler JL, Leavitt SW, Sherry R, Smith B, Weng E (2008) Consequences of more extreme precipitation regimes for terrestrial ecosystems. Bioscience 58:811–821CrossRefGoogle Scholar
  32. Krueger-Mangold J, Sheley R, Engel R (2006) Can R*s predict invasion in semi-arid grasslands? Biol Invasions 8:1343–1354CrossRefGoogle Scholar
  33. Lawlor DW, Tezara W (2009) Causes of decreased photosynthetic rate and metabolic capacity in water-deficient leaf cells: a critical evaluation of mechanisms and integration of processes. Ann Bot 103:561–579CrossRefPubMedGoogle Scholar
  34. Leishman MR, Thomson VP (2005) Experimental evidence for the effects of additional water, nutrients and physical disturbance on invasive plants in low fertility Hawkesbury Sandstone soils, Sydney, Australia. J Ecol 93:38–49CrossRefGoogle Scholar
  35. Loik ME (2007) Sensitivity of water relations and photosynthesis to summer precipitation pulses for Artemisia tridentata and Purshia tridentata. Plant Ecol 191:95–108CrossRefGoogle Scholar
  36. Monclus R, Dreyer E, Villar M, Delmotte FM, Delay D, Petit J, Barbaroux C, Le Thiec D, Brechet C, Brignolas F (2006) Impact of drought on productivity and water use efficiency in 29 genotypes of Populus deltoides × Populus nigra. New Phytol 169:765–777CrossRefPubMedGoogle Scholar
  37. Moran MD (2003) Arguments for rejecting the sequential Bonferroni in ecological studies. Oikos 100:403–405CrossRefGoogle Scholar
  38. Muth NZ, Pigliucci M (2007) Implementation of a novel framework for assessing species plasticity in biological invasions: responses of Centaurea and Crepis to phosphorus and water availability. J Ecol 95:1001–1013CrossRefGoogle Scholar
  39. Niinemets U, Valladares F, Ceulemans R (2003) Leaf-level phenotypic variability and plasticity of invasive Rhododendron ponticum and non-invasive Ilex aquifolium co-occurring at two contrasting European sites. Plant Cell Environ 26:941–956CrossRefPubMedGoogle Scholar
  40. Nobel PS, Sanderson J (1984) Rectifier-like activities of roots of two desert succulents. J Exp Bot 35:727–737CrossRefGoogle Scholar
  41. Noy-Meir I (1973) Desert ecosystems: environment and producers. Annu Rev Ecol Syst 4:25–51CrossRefGoogle Scholar
  42. Padgett PE, Allen EB (1999) Differential responses to nitrogen fertilization in native shrubs and exotic annuals common to mediterranean coastal sage scrub of California. Plant Ecol 144:93–101CrossRefGoogle Scholar
  43. Peek MS, Forseth IN (2009) Positive effects of soil nitrogen pulses on individuals can have negative consequences for population growth during drought in a herbaceous desert perennial. J Ecol 97:440–449CrossRefGoogle Scholar
  44. Quinn GP, Keough MJ (2002) Experimental design and data analysis for biologists. Cambridge University Press, CambridgeGoogle Scholar
  45. Reed HE, Seasteadt TR, Blair JM (2005) Ecological consequences of C4 grass invasion of a C4 grassland: a dilemma for management. Ecol Appl 15:1560–1569CrossRefGoogle Scholar
  46. Rejmanek M, Richardson DM, Pysek P (2005) Plant invasions and invasibility of plant communities. In: van der Maarel E (ed) Vegetation ecology. Blackwell Publishing, Oxford, pp 332–355Google Scholar
  47. Resco V, Ignace DD, Sun W, Huxman TE, Weltzin JF, Williams DG (2008) Chlorophyll fluorescence, predawn water potential and photosynthesis in precipitation pulse-driven ecosystems: implications for ecological studies. Funct Ecol 22:479–483CrossRefGoogle Scholar
  48. Rundel PW, Gustafson R (2005) Introduction to the Plant Life of Southern California: Coast to Foothills. University of California Press, Berkeley, CAGoogle Scholar
  49. Schwinning S, Ehleringer JR (2001) Water use trade-offs and optimal adaptations to pulse-driven arid ecosystems. J Ecol 89:464–480CrossRefGoogle Scholar
  50. Weltzin JF, McPherson GR (1997) Spatial and temporal soil moisture resource partitioning by trees and grasses in a temperate savanna, Arizona, USA. Oecologia 112:156–164CrossRefGoogle Scholar
  51. Williams DG, Black RA (1994) Drought response of a native and introduced Hawaiian grass. Oecologia 97:512–519CrossRefGoogle Scholar
  52. Yamashita N, Ishida A, Kushima H, Tanaka N (2000) Acclimation to sudden increase in light favoring an invasive over native trees in subtropical islands, Japan. Oecologia 125:412–419CrossRefGoogle Scholar
  53. Yang LH, Bastow JL, Spence KO, Wright AN (2008) What can we learn from resource pulses? Ecology 89:621–634CrossRefPubMedGoogle Scholar

Copyright information

© Springer Science+Business Media B.V. 2009

Authors and Affiliations

  1. 1.Department of Biological SciencesChapman UniversityOrangeUSA

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