Combined stresses in forests

Combined Stresses in Plants: Physiological, Molecular, and Biochemical Aspects

Volumn , Issue , 2015, Pages 223-244

  Mitchell, Patrick ^a   Wardlaw, Tim ^b   Pinkard, Libby ^a  

^a CSIRO   (Australia)

^b FORESTRY TASMANIA   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 84944586586     PISSN: None     EISSN: None     Source Type: Book    
DOI: 10.1007/978-3-319-07899-1_11     Document Type: Chapter

References (88)

1. Adams HD, Guardiola-claramonte M, Barron-gafford GA, Camilo J. Temperature sensitivity of drought-induced tree mortality portends increased regional die-off under global-change-type drought. Proc Natl Acad Sci U S A. 2009;106(17):7063-6.
2. Ainsworth EA, Rogers A. The response of photosynthesis and stomatal conductance to rising [CO2]: mechanisms and environmental interactions. Plant Cell Environ. 2007;30(3):258-70.
3. Akashi Y, Mueller-Dombois D. A landscape perspective of the Hawaiian rain forest dieback. J Veg Sci. 1995;6(4):449-64.
4. Allen CD, Macalady AK, Chenchouni H, Bachelet D, McDowell N, Vennetier M, et al. A global overview of drought and heat-induced tree mortality reveals emerging climate change risks for forests. For Ecol Manage. 2010;259(4):660-84. doi:10.1016/j.foreco.2009.09.001.
5. Ayres MP, Lombardero MaJ. Assessing the consequences of global change for forest disturbance from herbivores and pathogens. Sci Total Environ. 2000; 262(3):263-86. doi:10.1016/S0048-9697(00)00528-3.
6. Bansal S, Hallsby G, Lofvenius MO, Nilsson M-C. Synergistic, additive and antagonistic impacts of drought and herbivory on Pinus sylvestris: leaf, tissue and whole-plant responses and recovery. Tree Physiol. 2013;33(5):451-63.
7. Barrett-Lennard EG, Shabala SN. The waterlogging/salinity interaction in higher plants re-visited-focusing on the hypoxia-induced disturbance to K + homeostasis. Funct Plant Biol. 2013;40(9):872-82.
8. Boisvenue C, Running SW. Impacts of climate change on natural forest productivity-evidence since the middle of the 20th century. Glob Change Biol. 2006;12:862-82.
9. Bonan GB. Connecting mathematical ecosystems, real-world ecosystems, and climate science. New Phytol. 2014;202(3):731-3.
10. Breda N, Huc R, Granier A, Dreyer E. Temperate forest trees and stands under severe drought: a review of ecophysiological responses, adaptation processes and long-term consequences. Ann For Sci. 2006;63:625-44.
11. Brodribb TJ, Cochard H. Hydraulic failure defines the recovery and point of death. Plant Physiol. 2009;149:575-84.
12. Brodribb TJ, Bowman DJMS, Nichols S, Delzon S, Burlett R. Xylem function and growth rate interact to determine recovery rates after exposure to extreme water deficit. New Phytol. 2010;188(2):533-42.
13. Cable JM, Ogle K, Tyler AP, Pavao-Zuckerman Ma, Huxman TE. Woody plant encroachment impacts on soil carbon and microbial processes: results from a hierarchical Bayesian analysis of soil incubation data. Plant Soil. 2009;320:153-67.
14. Clements RJ, Ludlow MM. Frost Avoidance and Frost resistance in Centrosema virginianum. J Appl Ecol. 1977;14(2):551-66.
15. Davidson NJ, Battaglia M, Close DC. Photosynthetic responses to overnight frost in Eucalyptus nitens and E. globulus. Trees. 2004;18(3):245-52.
16. Dreesen FE, De Boeck HJ, Janssens IA, Nijs I. Do successive climate extremes weaken the resistance of plant communities? An experimental study using plant assemblages. Biogeosciences. 2014;11(1):109-21.
17. Duan H, Amthor JS, Duursma RA, O’Grady AP, Choat B, Tissue DT. Carbon dynamics of eucalypt seedlings exposed to progressive drought in elevated [CO2] and elevated temperature. Tree Physiol. 2013;33(8):779-92.
18. Duan H, Duursma RA, Huang G, Smith RA, Choat B, O’Grady AP, et al. Elevated [CO2] does not ameliorate the negative effects of elevated temperature on drought-induced mortality in Eucalyptus radiata seedlings. Plant Cell Environ. 2014;37:1598-613.
19. Engelbrecht B, Kursar T. Comparative drought-resistance of seedlings of 28 species of co-occurring tropical woody plants. Oecologia. 2003;136(3):383-93.
20. Fensham RJ, Fairfax RJ. Drought-related tree death of savanna eucalypts: species susceptibility, soil conditions and root architecture. J Veg Sci. 2007;18(1):71-80.
21. Frank JM, Massman WJ, Ewers BE, Huckaby LS, Negron JF. Ecosystem CO2/H2O fluxes are explained by hydraulically limited gas exchange during tree mortality from spruce bark beetles. J Geophys Res Biogeosci. 2014;119:1195-1215. doi:10.1002/2013JG002597.
22. Galiano L, Martinez-Vilalta J, Lloret F. Carbon reserves and canopy defoliation determine the recovery of Scots pine 4 year after a drought episode. New Phytol. 2011;190(3):750-9.
23. Galle A, Feller U. Changes of photosynthetic traits in beech saplings (Fagus sylvatica) under severe drought stress and during recovery. Physiol Plant. 2007;131(3):412-21.
24. Garrett KA, Dendy SP, Frank EE, Rouse MN, Travers SE. Climate change effects on plant disease: genomes to ecosystems. Annu Rev Phytopathol. 2006;44(1):489-509.
25. Gieger T, Thomas FM. Effects of defoliation and drought stress on biomass partitioning and water relations of Quercus robur and Quercuspetraea. Basic Appl Ecol. 2002;3(2):171-81.
26. Grime JP. Evidence for the existence of three primary strategies in plants and its relevance to ecological and evolutionary theory. Am Nat. 1977;111(982):1169-94.
27. Hartmann H, Ziegler W, Kolle O, Trumbore S. Thirst beats hunger-declining hydration during drought prevents carbon starvation in Norway spruce saplings. New Phytol. 2013;200:340-9.
28. Holtta T, Mencuccini M, Nikinmaa E. Linking phloem function to structure: Analysis with a coupled xylem-phloem transport model. J Theor Biol. 2009;259(2):325-37.
29. Hsiao TC, Acevedo E, Fereres E, Henderson DW. Water stress, growth, and osmotic adjustment. Philos Trans R Soc Lond B Biol Sci. 1976;273(927):479-500.
30. Jacquet J-S, Bosc A, O’Grady AP, Jactel. H. Pine growth response to processionary moth defoliation across a 40 year age chronosequence. For Ecol Manage. 2013;293:29-38.
31. Jacquet JS, Bosc A, O’Grady A, Jactel H. Combined effects of defoliation and water stress on pine growth and non-structural carbohydrates. Tree Physiol. 2014;34(4): 1-10.
32. Jactel H, Petit J, Desprez-Loustau M-L, Delzon S, Piou D, Battisti A, et al. Drought effects on damage by forest insects and pathogens: a meta-analysis. Glob Change Biol. 2012;18(1):267-76.
33. Jonsson AM, Schroeder LM, Lagergren F, Anderbrant O, Smith B. Guess the impact of Ips ty-pographus—an ecosystem modelling approach for simulating spruce bark beetle outbreaks. Agric For Meteorol. 2012;166-167(0):188-200.
34. Jurskis V. Eucalypt decline in Australia, and a general concept of tree decline and dieback. For Ecol Manage. 2005;215(1-3):1-20. doi:10.1016/j.foreco.2005.04.026.
35. Koepke D, Kolb T, Adams H. Variation in woody plant mortality and dieback from severe drought among soils, plant groups, and species within a northern Arizona ecotone. Oecologia. 2010;163(4):1079-90.
36. Lambers H, Chapin FS, Pons TL. Assumptions and approaches. Plant physiological ecology. New York: Springer; 2008. p. 154-204.
37. Landsberg J. Water stress, leaf nutrients and defoliation: a model of dieback in rural eucalypts. Aust J Ecol. 1983;8:27-41.
38. Larsen JB. Testing winter desiccation resistance for species and provenance selection at timber-lines. In: Alden J, editor. Forest development in cold climates. New York: Plenum Press; 1993. p. 59-64.
39. Li Z, Apps MJ, Kurz WA, Banfield E. Temporal changes of forest net primary production and net ecosystem production in west central Canada associated with natural and anthropogenic disturbances. Can J For Res. 2003;33(12):2340-51. doi:10.1139/x03-168.
40. Liu C-C, Liu Y-G, Guo K, Zheng Y-R, Li G-Q, Yu L-F, et al. Influence of drought intensity on the response of six woody karst species subjected to successive cycles of drought and rewatering. Physiol Plant. 2010;139(1):39-54.
41. Lloret F, Siscart D, Dalmases C. Canopy recovery after drought dieback in holm-oak Mediterranean forests of Catalonia (NE Spain). Glob Change Biol. 2004;10(12):2092-9.
42. Lloret F, Escudero A, Iriondo JM, Martinez-Vilalta J, Valladares F. Extreme climatic events and vegetation: the role of stabilizing processes. Glob Change Biol. 2012;18(3):797-805.
43. Loehle C, LeBlanc D. Model-based assessments of climate change effects on forests: a critical review. Ecol Modell. 1996;90(1):1-31. doi:10.1016/0304-3800(96)83709-4.
44. Long SP, East TM, Baker NR. Chilling damage to photosynthesis in Young Zea mays: I. Effects of light and temperature variation on photosynthetic CO2 assimilation. J Exp Bot. 1983;34(2):177-88.
45. Lyon B. Southern Africa summer drought and heat waves: observations and coupled model behavior. J Climate. 2011;22(22):6033-46. doi:10.1175/2009JCLI3101.1.
46. Manion PD. Decline diseases of complex biotic and abiotic origin. Tree disease concepts. Engle-wood Cliffs: Prentice-Hall; 1981. p. 324-39.
47. Matusick G, Ruthrof K, Brouwers N, Dell B, Hardy GJ. Sudden forest canopy collapse corresponding with extreme drought and heat in a Mediterranean-type eucalypt forest in southwestern Australia. Eur J Forest Res. 2013;132(3):497-510.
48. McDowell N, Pockman WT, Allen CD, Breshears DD, Cobb N, Kolb T, et al. Mechanisms of plant survival and mortality during drought: why do some plants survive while others succumb to drought? New Phytol. 2008;178(4):719-39.
49. McDowell NG, Beerling DJ, Breshears DD, Fisher RA, Raffa KF, Stitt M. The interdependence of mechanisms underlying climate-driven vegetation mortality. Trends Ecol Evol. 2011;26(10):523-32.
50. McDowell NG, Fisher RA, Xu C, Domec JC, Holtta T, Mackay DS, et al. Evaluating theories of drought-induced vegetation mortality using a multimodel-experiment framework. New Phytol. 2013;200(2):304-21.
51. Metcalf CJE, McMahon SM, Clark JS. Overcoming data sparseness and parametric constraints in modeling of tree mortality: a new nonparametric Bayesian model. Can J For Res. 2009;39(9):1677-87. doi:10.1139/X09-083.
52. Mitchell PJ, Veneklaas EJ, Lambers H, Burgess SSO. Using multiple trait associations to define hydraulic functional types in plant communities of south-western Australia. Oecologia. 2008;158:385-97.
53. Mitchell PJ, Battaglia M, Pinkard EA. Counting the costs of multiple stressors: is the whole greater than the sum of the parts? Tree Physiol. 2013;33(5):447-50.
54. Mitchell PJ, O’Grady AP, Tissue DT, White DA, Ottenschlaeger ML, Pinkard EA. Drought response strategies define the relative contributions of hydraulic dysfunction and carbohydrate depletion during tree mortality. New Phytol. 2013;197(3):862-72.
55. Mitchell PJ, O’Grady AP, Hayes KR, Pinkard EA. Exposure of trees to drought-induced die-off is defined by a common climatic threshold across different vegetation types. Ecol Evol. 2014;4(7):1088-101.
56. Mitchell PJ, O’Grady AP, Tissue DT, Worledge D, Pinkard EA. Co-ordination of growth, gas exchange and hydraulics define the carbon safety margin in tree species with contrasting drought strategies. Tree Physiol. 2014;34:443-58.
57. Mueller-Dombois D. Perspectives for an etiology of stand-level dieback. Annu Rev Ecol Syst. 1986;17:221-43. (ArticleType: research-article/Full publication date: 1986/Copyright © 1986 Annual Reviews).
58. Mueller-Dombois D. Natural dieback in forests. Bioscience. 1987;37(8):575-83.
59. Mueller-Dombois D. Towards a unifying theory for stand-level dieback. Geojournal. 1988;17(2):249-51.
60. Munns R, Termaat A. Whole-plant responses to salinity. Funct Plant Biol. 1986;13(1):143-60.
61. Niinemets U. Responses of forest trees to single and multiple environmental stresses from seedlings to mature plants: Past stress history, stress interactions, tolerance and acclimation. For Ecol Manage. 2010;260(10):1623-39.
62. Ogle K, Barber J. Bayesian data-model integration in plant physiological and ecosystem ecology. In: Luttge U, Beyschlag W, Murata J, editors. Progress in Botany. Springer Berlin Heidelberg; 2008. p. 281-311.
63. Penuelas J, Sardans J, Estiarte M, Ogaya R, Carnicer J, Coll M, et al. Evidence of current impact of climate change on life: a walk from genes to the biosphere. Glob Change Biol. 2013;19(8):2303-38.
64. Pinkard EA, Eyles A, O’Grady AP. Are gas exchange responses to resource limitation and defoliation linked to source: sink relationships? Plant Cell Environ. 2011;34(10):1652-65.
65. Pinkard EA, Battaglia M, Roxburgh S, O’Grady AP. Estimating forest net primary production under changing climate: adding pests into the equation. Tree Physiol. 2011;31(7):686-99.
66. Pook EW, Forrester R. Factors influencing dieback and drought-affected dry sclerophyll forest tree species. Aust For Res. 1984;14:201-17.
67. Poyatos R, Aguade D, Galiano L, Mencuccini M, Martinez-Vilalta J. Drought-induced defoliation and long periods of near-zero gas exchange play a key role in accentuating metabolic decline of Scots pine. New Phytol. 2013;200:388-401.
68. Rammig A, Jupp T, Thonicke K, Tietjen B, Heinke J, Ostberg S, et al. Estimating the risk of Amazonian forest dieback. New Phytol. 2010;187(3):694-706.
69. Repo T, Kalliokoski T, Domisch T, Lehto T, Mannerkoski H, Sutinen S, et al. Effects of timing of soil frost thawing on Scots pine. Tree Physiol. 2005;25(8):1053-62.
70. Repo T, Lehto T, Finer L. Delayed soil thawing affects root and shoot functioning and growth in Scots pine. Tree Physiol. 2008;28(10):1583-91.
71. Rivas-Ubach A, Gargallo-Garriga A, Sardans J, Oravec M, Mateu-Castell L, Perez-Trujillo M, et al. Drought enhances folivory by shifting foliar metabolomes in Quercus ilex trees. New Phytol. 2014;202(3):874-85.
72. Rouault G, Candau J-N, Lieutier F, Nageleisen L-M, Martin J-C, Warzee N. Effects of drought and heat on forest insect populations in relation to the 2003 drought in Western Europe. Ann For Sci. 2006;63(6):613-24.
73. Sala A, Woodruff DR, Meinzer FC. Carbon dynamics in trees: feast or famine? Tree Physiol. 2012;32(6):764-75.
74. Selye H. A syndrome produced by diverse nocuous agents. Nature. 1936;138:32.
75. Shan Y. Phenological disorder induced by atmospheric nitrogen deposition: original causes of pine forest decline over Japan. Part II. Relationship among earlier phenological development, extreme of minimum air temperature, and forest decline of pines over the Japan. Water Air Soil Pollut. 2000;117(1-4):205-15.
76. Steinbauer MJ. Specific leaf weight as an indicator of juvenile leaf toughness in Tasmanian bluegum (Eucalyptus globulus ssp. globulus): implications for insect defoliation. Aust For. 2001;64(1):32-7. doi:10.1080/00049158.2001.10676158.
77. Steinberg CEW, Sturzenbaum SR, Menzel R. Genes and environment-striking the fine balance between sophisticated biomonitoring and true functional environmental genomics. Sci Total Environ. 2008;400(1-3):142-61.
78. Stone C. Bell-miner-associated dieback at the tree crown scale: a multi-trophic process. Aust For. 2005;68(4):237-41. doi:10.1080/00049158.2005.10674971.
79. Trought M, Drew M. The development of waterlogging damage in young wheat plants in anaerobic solution cultures. J Exp Bot. 1980;31:1575-85.
80. Tyree MT, Sperry JS. Do woody plants operate near the point of catastrophic xylem dysfunction caused by dynamic water stress? Answers from a model. Plant Physiol. 1988;88:574-80.
81. Tyree MT, Sperry JS. Vulnerability of xylem to cavitation and embolism. Ann Rev Plant Physiol Plant Mol Biol. 1989;40(1):19-36.
82. van der Moezel PG, Watson LE, Bell DT. Gas exchange responses of two Eucalyptus species to salinity and waterlogging. Tree Physiol. 1989;5(2):251-7.
83. van Mantgem PJ, Stephenson NL, Fule PZ, et al. Widespread increase of tree mortality rates in the western United States. Science. 2009;323(5913):521-4.
84. Vautard R, Yiou P, D’Andrea F, de Noblet N, Viovy N, Cassou C, et al. Summertime European heat and drought waves induced by wintertime Mediterranean rainfall deficit. Geophys Res Lett. 2007;34(7):1-5.
85. Wardell-Johnson G, Stone C, Recher H, Lynch AJJ. A review of eucalypt dieback associated with bell miner habitat in south-eastern Australia. Aust For. 2005;68(4):231-6. doi:10.1080/00049 158.2005.10674970.
86. Wargo P. Consequences of environmental stress on oak: predisposition to pathogens. Ann For Sci. 1996;53(2-3):359-68.
87. Warren JM, Norby RJ, Wullschleger SD. Elevated CO2 enhances leaf senescence during extreme drought in a temperate forest. Tree Physiol. 2011;31(2):117-30.
88. White TCR. The abundance of invertebrate herbivores in relation to the availability of nitrogen in stressed food plants. Oecologia. 1984;63(1):90-105.