Integrative leaf-level phytotoxic ozone dose assessment for forest risk modelling

Developments in Environmental Science

Volumn 13, Issue , 2013, Pages 267-288

  Dizengremel, Pierre ^a,b   Jolivet, Yves ^a,b   Tuzet, Andrée ^c   Ranieri, Annamaria ^d   Le Thiec, Didier ^a,b  

^a UNIVERSITÉ DE LORRAINE   (France)

^b LERFoB   (France)

^c CEMAGREF   (France)

^d UNIVERSITY OF PISA   (Italy)

Author keywords

Detoxification capacity; Modelling; Ozone phytotoxicity; Primary carbon metabolism; Redox power; Risk assessment; Stomatal conductance

Indexed keywords

EID: 84888326686     PISSN: 14748177     EISSN: None     Source Type: Book Series    
DOI: 10.1016/B978-0-08-098349-3.00013-X     Document Type: Chapter

References (91)

1. Ashmore M.R. Assessing the future global impacts of ozone on vegetation. Plant Cell Environ. 2005, 28:949-964.
2. Bagard M., Le Thiec D., DelacÔte E., Hasenfratz-Sauder M.P., Banvoy J., Gérard J., Dizengremel P., Jolivet Y. Ozone-induced changes in photosynthesis and photorespiration of hybrid poplar in relation to the developmental stage of the leaves. Physiol. Plant. 2008, 134:559-574.
3. Baier M., Kandlbinder A., Golldack D., Dietz K.J. Oxidative stress and ozone: perception, signalling and response. Plant Cell Environ. 2005, 28:1012-1020.
4. Barnosky A.D., Hadly E.A., Bascompte J., Berlow E.L., Brown J.H., Fortelius M., Getz W.M., Harte J., Hastings A., Marquet P.A., Martinez N.D., Mooers A., Roopnarine P., Vermeij G., Williams J.W., Gillespie R., Kitzes J., Marshall C., Matzke N., Mindell D.P., Revilla E., Smith A.B. Approaching a state shift in Earth's biosphere. Nature 2012, 486:52-58.
5. Booker F.L., Burkey K.O., Jones A.M. Re-evaluating the role of ascorbic acid and phenolic glycosides in ozone scavenging in the leaf apoplast of Arabidopsis thaliana L. Plant Cell Environ. 2012, 35:1456-1466.
6. Brosché M., Merilo E., Mayer F., Pechter P., Puzorjova I., Brader G., Kangasjarvi J., Kollist H. Natural variation in ozone sensitivity among Arabidopsis thaliana accessions and its relation to stomatal conductance. Plant Cell Environ. 2010, 33:914-925.
7. Cabané M., Pireaux J.-C., Léger E., Weber E., Dizengremel P., Pollet B., Lapierre C. Condensed lignins are synthesized in poplar leaves exposed to ozone. Plant Physiol. 2004, 134:586-594.
8. 3 uptake to gene expression adjustment. Environ. Pollut. 2009, 157:1461-1469.
9. Castagna A., Nali C., Ciompi S., Lorenzini G., Soldatini G.F., Ranieri A. Ozone exposure affects photosynthesis of pumpkin (Cucurbita pepo) plants. New Phytol. 2001, 152:223-229.
10. Chameides W.L. The chemistry of ozone deposition to plant leaves: role of ascorbic acid. Environ. Sci. Technol. 1989, 23:595-600.
11. Dalstein L., Torti X., Le Thiec D., Dizengremel P. Physiological study of declining Pinus cembra (L.) trees in southern France. Trees 2002, 16:299-305.
12. 3 fumigation on the activity of some Calvin cycle enzymes in two poplar clones. Photosynthetica 2002, 40:121-126.
13. 3. Plant Physiol. Biochem. 2003, 41:485-493.
14. Dghim A.A., Dumont J., Hasenfratz-Sauder M.P., Dizengremel P., Le Thiec D., Jolivet Y. Capacity for NADPH regeneration in the leaves of two poplar genotypes differing in ozone sensitivity. Physiol. Plant 2013, 148:36-50.
15. D'Haese D., Vandermeiren K., Asard H., Horemans N. Other factors than apoplastic ascorbate contribute to the differential ozone tolerance of two clones of Trifolium repens L. Plant Cell Environ. 2005, 28:623-632.
16. 2, ethylene and salicylic acid. New Phytol. 2005, 168:351-364.
17. 3 influx?. Tree Physiol. 2008, 28:1761-1772.
18. Dizengremel P. Effects of ozone on the carbon metabolism of forest trees. Plant Physiol. Biochem. 2001, 39:729-742.
19. Dizengremel P., Sasek T., Brown K.J., Richardson C.J. Ozone-induced changes in primary carbon metabolism enzymes of loblolly pine needles. J. Plant Physiol. 1994, 144:300-306.
20. Dizengremel P., Le Thiec D., Bagard M., Jolivet Y. Ozone risk assessment for plants: central role of metabolism-dependent changes in reducing power. Environ. Pollut. 2008, 156:11-15.
21. Dizengremel P., Le Thiec D., Hasenfratz-Sauder M.P., Vaultier M.N., Bagard M., Jolivet Y. Metabolic-dependent changes in plant cell redox power after ozone exposure. Plant Biol. 2009, 11:35-42.
22. Dizengremel P., Vaultier M.N., Le Thiec D., Cabané M., Bagard M., Gérant D., Gérard J., Dghim A.A., Richet N., Afif D., Pireaux J.C., Hasenfratz-Sauder M.P., Jolivet Y. Phosphoenolpyruvate is at the crossroads of leaf metabolic responses to ozone stress. New Phytol. 2012, 195:512-517.
23. Dumont, J., Spicher, F., Montpied, P., Dizengremel, P., Jolivet, Y., Le Thiec, D., (unpublished). Effects of ozone on stomatal responses to environmental parameters (blue light, red light, CO2 and vapour pressure deficit) in three Populus deltoides x nigra genotypes. Environ. Pollut. 173, 85-96.
24. Eckey-Kaltenbach H., Ernst D., Heller W., Sandermann H. Biochemical plant responses to ozone: IV. Cross-induction of defensive pathways in parsley (Petroselinum crispum L.) plants. Plant Physiol. 1994, 104:67-74.
25. Einig W., Lauxmann U., Hauch B., Hampp R., Landolt W., Maurer S., Matyssek R. Ozone-induced accumulation of carbohydrates changes enzyme activities of carbohydrate metabolism in birch leaves. New Phytol. 1997, 137:673-680.
26. Ernst D. Integrated studies on abiotic stress defence in trees: the case of ozone. Dev. Environ. Sci. 2013, 13:289-307.
27. Fares S., Oksanen E., Lännenpää M., Julkunen-Tiito R., Loreto F. Volatile emissions and phenolic compound concentrations along a vertical profile of Populus nigra leaves exposed to realistic ozone concentrations. Photosynth. Res. 2010, 104:61-74.
28. Fontaine V., Pelloux J., Podor M., Afif D., Gérant D., Grieu P., Dizengremel P. Carbon fixation in Pinus halepensis submitted to ozone. Opposite response of ribulose-1,5-bisphosphate carboxylase:oxygenase and phosphoenolpyruvate carboxylase. Physiol. Plant. 1999, 105:187-192.
29. Foyer C.H., Noctor G. Redox homeostasis and antioxidant signaling: a metabolic interface between stress perception and physiological responses. Plant Cell 2005, 17:1866-1875.
30. Gaucher C., Costanzo N., Afif D., Mauffette Y., Chevrier N., Dizengremel P. The impact of elevated ozone and carbon dioxide on young Acer saccharum seedlings. Physiol. Plant. 2003, 117:392-402.
31. Grace S.C. Phenolics as antioxidants. Antioxidants and Reactive Oxygen Species in Plants 2005, 141-168. Blackwell Publishing Ltd, Oxford, UK. N. Smirnoff (Ed.).
32. 3 levels in the photosynthetic light and dark reactions of European beech (Fagus sylvatica). New Phytol. 1999, 144:95-107.
33. Häikiö E., Freiwald V., Julkunen-Tiito R., Beuker E., Holopainen T., Oksanen E. Differences in leaf characteristics between ozone-sensitive and ozone-tolerant hybrid aspen (Populus tremula x Populus tremuloides) clones. Tree Physiol. 2009, 29:53-66.
34. 2, temperature, precipitation and ozone on carbon and water cycles of an upland-oak forest: incorporating experimental results into model simulations. Glob. Chang. Biol. 2005, 11:1402-1423.
35. Heath R. Modification of the biochemical pathways of plants induced by ozone: what are the various routes of change?. Environ. Pollut. 2008, 155:453-463.
36. Jaspers P., Kangasjärvi J. Reactive oxygen species in abiotic stress signaling. Physiol. Plant. 2010, 138:405-413.
37. Kangasjärvi J., Jaspers P., Kollist H. Signalling and cell death in ozone-exposed plants. Plant Cell Environ. 2005, 28:1021-1036.
38. Kasurinen A., Biasi C., Holopainen T., Ronsi M., Mäenpää M., Oksanen E. Interactive effects of elevated ozone and temperature on carbon allocation of silver birch (Betula pendula) genotypes in an open-air field exposure. Tree Physiol. 2012, 32:737-751.
39. Koch J.R., Scherzer A.J., Eshita S.M., Davis K.R. Ozone sensitivity in hybrid poplar is correlated with a lack of defense-gene activation. Plant Physiol. 1998, 118:1243-1252.
40. Kontunen-Soppela S., Ossipov V., Ossipova S., Oksanen E. Shift in birch leaf metabolome and carbon allocation during long-term open-field ozone exposure. Glob. Chang. Biol. 2007, 13:1053-1067.
41. 3 concentrations throughout two subsequent growing seasons. Glob. Chang. Biol. 2005, 11:1387-1401.
42. Laisk A., Kull O., Moldau H. Ozone concentration in leaf intercellular air spaces is close to zero. Plant Physiol. 1989, 90:1163-1167.
43. Langebartels C., Schraudner M., Heller W., Ernst D., Sandermann H. Oxidative stress and defense reactions in plants exposed to air pollutants and UV-B radiation. Oxidative Stress in Plants 2002, 105-135. Taylor & Francis, London, UK. D. Inzé, M. Van Montagu (Eds.).
44. 3 on forests: phytochemistry, trophic interactions, and ecosystem dynamics. J. Chem. Ecol. 2010, 36:2-21.
45. Liu X., Kozovits A.R., Grams T.E.E., Blaschke H., Rennenberg H., Matyssek R. Competition modifies effects of enhanced ozone/carbon dioxide concentrations on carbohydrate and biomass accumulation in juvenile Norway spruce and European beech. Tree Physiol. 2004, 24:1045-1055.
46. Löw M., Herbinger K., Nunn A.J., Häberle K.-H., Leuchner M., Heerdt C., Werner H., Wipfler P., Pretzsch H., Tausz M., Matyssek R. Extraordinary drought of 2003 overrules ozone impact on adult beech trees (Fagus sylvatica). Trees 2006, 20:539-548.
47. Matyssek R., Innes J.L. Ozone-a risk factor for trees and forests in Europe?. Water Air Soil Pollut. 1999, 116:199-226.
48. Matyssek R., Sandermann H. Impact of ozone on trees: an ecophysiological perspective. Prog. Bot. 2003, 64:349-404.
49. 3 stress in forest trees. Plant Biol. 2006, 8:11-17.
50. 3 flux concept for European forest trees. Environ. Pollut. 2007, 146:587-607.
51. Matyssek R., Sandermann H., Wieser G., Booker F., Cieslik S., Musselman R., Ernst D. The challenge of making ozone risk assessment for forest trees more mechanistic. Environ. Pollut. 2008, 156:567-582.
52. Matyssek R., Wieser G., Ceulemans R., Rennenberg H., Pretzsch K., Löw M., Nunn A.J., Werner H., Wipfler P., Osswald W., Nikolova P., Hanke D.E., Kraigher H., Tausz M., Bahnweg G., Kitao M., Dieler J., Sandermann H., Herbinger K., Grebenc T., Blumenröther M., Deckmyn G., Grams T.E.E., Heerdt C., Leuchner M., Fabian P., Häberle K.H. Enhanced ozone strongly reduces carbon sink strength of adult beech (Fagus sylvatica)-resume from the free air fumigation study at Kranzberg Forest. Environ. Pollut. 2010, 158:2527-2532.
53. Matyssek R., Wieser G., Calfapietra C., de Vries W., Dizengremel P., Ernst D., Jolivet Y., Mikkelsen T.T., Mohren G.M.J., Le Thiec D., Tuovinen J.P., Weatherall A., Paoletti E. Forests under climate change and air pollution: gaps in understanding and future directions for research. Environ. Pollut. 2012, 160:57-65.
54. Matyssek R., Koricheva J., Schnyder H., Ernst D., Munch J.C., Osswald W., Pretzsch H. The balance between resource sequestration and retention: a challenge in plant science. Ecological Studies 2012, vol. 220:3-24. Springer, Berlin. R. Matyssek, H. Schnyder, W. Osswald, D. Ernst, J.C. Munch, H. Pretzsch (Eds.).
55. Matyssek R., Schnyder H., Osswald W., Ernst D., Munch J.C., Pretzsch H. Growth and defence in plants-resource allocation at multiple scales. Ecological Studies 2012, vol. 220:467. Springer, Berlin.
56. Matyssek R., Wieser G., Fleischmann F., Grünhage L. Ozone research, quo vadis? Lessons from the Kranzberg forest experiment. Dev. Environ. Sci. 2013, 13:103-129.
57. McLaughlin S.B., Nosal M., Wullschleger S.D., Sun G. Interactive effects of ozone and climate on tree growth and water use in a southern Appalachian forest in the USA. New Phytol. 2007, 174:109-124.
58. Musselman R.C., Lefohn A.S., Massman W.J., Heath R.L. A critical review and analysis of the use of exposure- and flux-based ozone indices for predicting vegetation effects. Atmos. Environ. 2006, 40:1869-1888.
59. Noctor G. Metabolic signalling in defence and stress: the central roles of soluble redox couples. Plant Cell Environ. 2006, 29:409-425.
60. Noctor G., Mhamdi A., Chaouch S., Han Y., Neukermans J., Queval G., Foyer C.H. Glutathione in plants: an integrated overview. Plant Cell Environ. 2012, 35:454-484.
61. 2 and climate warming. Dev. Environ. Sci. 2013, 13:309-329.
62. 2 ameliorate tree response to ozone? A review on stomatal responses. Environ. Pollut. 2005, 137:483-493.
63. Paoletti E., Manning W.J. Toward a biologically significant and usable standard for ozone that will also protect plants. Environ. Pollut. 2007, 150:85-95.
64. Pasqualini S., Della Torre G., Ferranti F., Ederli L., Piccioni C., Reale L., Antonielli M. Salicylic acid modulates ozone-induced hypersensitive cell death in tobacco plants. Physiol. Plant. 2002, 115:204-212.
65. Pell E.J., Eckardt N., Enyedi A.J. Timing of ozone stress and resulting status of ribulose bisphosphate carboxylase/oxygenase and associated net photosynthesis. New Phytol. 1992, 120:397-405.
66. Plöchl M., Lyons T., Ollerenshaw J., Barnes J. Simulating ozone detoxification in the leaf apoplast through the direct reaction with ascorbate. Planta 2000, 210:454-457.
67. Polle A. Dissecting the superoxide dismutase-ascorbate-glutathione pathway in chloroplasts by metabolic modeling. Computer simulations as a step towards flux analysis. Plant Physiol. 2001, 126:445-462.
68. Polle A., Wieser G., Havranek W.M. Quantification of ozone influx and apoplastic ascorbate content in needles of Norway spruce trees (Picea abies L. Karst.) at high altitude. Plant Physiol. 1995, 94:312-319.
69. 3-sensitivity in two polar clones. J. Plant Physiol. 1999, 150:250-255.
70. Rao M.V., Lee H.I., Davis K.R. Ozone-induced ethylene production is dependent on salicylic acid, and both salicylic acid and ethylene act in concert to regulate ozone-induced cell death. Plant J. 2002, 32:447-456.
71. 3 on net photosynthesis, dark respiration and chlorophyll contents in aging hybrid poplar leaves. Plant Physiol. 1983, 73:291-296.
72. Renaut J., Bohler S., Hausman J.F., Hoffmann L., Sergeant K., Ashan N., Jolivet Y., Dizengremel P. The impact of atmospheric composition on plants: a case study of ozone on poplar. Mass Spectrom. Rev. 2009, 28:495-516.
73. 3 on antioxidant capacity and gas exchange in Betula pendula saplings. Planta 2009, 230:419-427.
74. Saleem A., Loponen J., Pihlaja K., Oksanen E. Effects of long-term open-field ozone exposure on leaf phenolics of European silver birch (Betula pendula Roth.). J. Chem. Ecol. 2001, 27:1049-1062.
75. 13C in Betula pendula. Oecologia 1995, 103:397-406.
76. Sehmer L., Fontaine V., Antoni F., Dizengremel P. Effects of ozone and elevated atmospheric carbon dioxide on carbohydrate metabolism of spruce needles. Catabolic and detoxification pathways. Physiol. Plant. 1998, 102:605-611.
77. Sitch S., Cox P.M., Collins W.J., Huntingford C. Indirect oxidative forcing of climate change through ozone effects on the land-carbon sink. Nature 2007, 448:791-795.
78. Sun G., McLaughlin S.B., Porter J.H., Uddling J., Mulholland P.J., Adams M.B., Pederson N. Interactive influences of ozone and climate on streamflow of forested watersheds. Glob. Chang. Biol. 2012, 18:3395-3409.
79. Sweetlove L.J., Beard K.F.M., Nunes-Nesi A., Fernie A.R., Ratcliffe R.G. Not just a circle: flux modes in the plant TCA cycle. Trends Plant Sci. 2010, 15:462-470.
80. Tausz M., Grulke N.E., Wieser G. Defense and avoidance of ozone under global change. Environ. Pollut. 2007, 147:525-531.
81. Templer P.H., Reinmann A.B. Multi-factor global change experiments: what have we learned about terrestrial carbon storage and exchange?. New Phytol. 2011, 192:797-800.
82. Tuzet A., Perrier A., Loubet B., Cellier P. Modelling ozone deposition fluxes: the relative roles of deposition and detoxification processes. Agric. Forest Meteorol. 2011, 151:480-492.
83. 3 enrichment. Environ. Pollut. 2010, 158:2023-2031.
84. 2, on tree leaf chemistry and insect herbivore performance: a meta-analysis. Glob. Chang. Biol. 2007, 13:184-201.
85. Wieser G., Tegischer K., Tausz M., Häberle K.H., Grams T.E.E., Matyssek R. Age effects on Norway spruce (Picea abies) susceptibility to ozone uptake: a novel approach relating stress avoidance to defense. Tree Physiol. 2002, 22:583-590.
86. Wild A., Schmitt V. Diagnosis of damage to Norway spruce (Picea abies) through biochemical criteria. Physiol. Plant. 1995, 93:375-382.
87. Wittig V.E., Ainsworth E.A., Long S.P. To what extent do current and projected increases in surface ozone affect photosynthesis and stomatal conductance of trees? A meta-analytic review of the last 3 decades of experiments. Plant Cell Environ. 2007, 30:1150-1162.
88. Wittig V.E., Ainsworth E.A., Naidu S.L., Karnosky D.F., Long S.P. Quantifying the impact of current and future tropospheric ozone on tree biomass, growth, physiology and biochemistry: a quantitative meta-analysis. Glob. Chang. Biol. 2009, 15:396-424.
89. 3?. Environ. Pollut. 2001, 115:473-481.
90. Zechmann B. Subcellular distribution of ascorbate in plants. Plant Signal. Behav. 2011, 6:360-363.
91. Zinser C., Ernst D., Sandermann H. Induction of stilbene synthase and cinnamyl alcohol dehydrogenase mRNA in Scots pine (Pinus sylvestris L.) seedlings. Planta 1998, 204:169-176.