Oxygen and environmental stress in plants: and evolutionary context

Contemporary plant species show a wide range of responses to oxidative attack. Much of this variation may reflect the different environmental selective pressures operating at different geological periods over the course of angiosperm evolution. Evidence is provided to show that the wide range of contemporary responses to oxidative stress may directly reflect the persistence of genes controlling free radical processes under environments of the past.

[1]  M. Merzlyak,et al.  Free radical metabolism, pigment degradation and lipid peroxidation in leaves during senescence , 1994 .

[2]  G. Hendrỳ,et al.  The mechanisms of desiccation tolerance in developing seeds , 1993, Seed Science Research.

[3]  G. Hendrỳ Oxygen, free radical processes and seed longevity , 1993, Seed Science Research.

[4]  F. J. Corpas,et al.  Salt-induced oxidative stress mediated by activated oxygen species in pea leaf mitochondria , 1993 .

[5]  L. Froget,et al.  Evidence for a K/T impact event in the Pacific Ocean , 1993, Nature.

[6]  C. Swisher,et al.  Implications of an exceptional fossil flora for Late Cretaceous vegetation , 1993, Nature.

[7]  G. Wingsle,et al.  Influence of SO2 and NO2 Exposure on Glutathione, Superoxide Dismutase and Glutathione Reductase Activities in Scots Pine Needles , 1993 .

[8]  A. Raschi,et al.  The Antioxidant Status of Soybean (Glycine max) Leaves Grown Under Natural CO2 Enrichment in the Field , 1993 .

[9]  G. Hendrỳ,et al.  A free radical ubiquitously associated with senescence in plants: evidence for a quinone. , 1993, Free radical research communications.

[10]  W. Seel,et al.  Free radical processes and loss of seed viability during desiccation in the recalcitrant species Quercus robur L. , 1992, The New phytologist.

[11]  M. Becana,et al.  Transition metals in legume root nodules: iron-dependent free radical production increases during nodule senescence. , 1992, Proceedings of the National Academy of Sciences of the United States of America.

[12]  A. Baker,et al.  Cadmium tolerance and toxicity, oxygen radical processes and molecular damage in cadmium‐tolerant and cadmium‐sensitive clones of Holcus lanatus L. , 1992 .

[13]  J. Lee,et al.  The Combined Effects of Desiccation and Irradiance on Mosses from Xeric and Hydric Habitats , 1992 .

[14]  R. Crawford,et al.  Influence of L-Ascorbic Acid on Post-anoxic Growth and Survival of Chickpea Seedlings (Cicer arietinum L.) , 1992 .

[15]  H. Marschner,et al.  Magnesium deficiency and high light intensity enhance activities of superoxide dismutase, ascorbate peroxidase, and glutathione reductase in bean leaves. , 1992, Plant physiology.

[16]  R. Ponquett,et al.  Lipid autoxidation and seed ageing: putative relationships between seed longevity and lipid stability , 1992, Seed Science Research.

[17]  F. Navari-Izzo,et al.  Water Stress and Free Radical Mediated Changes in Sunflower Seedlings , 1992 .

[18]  E. Benson,et al.  The detection of lipid peroxidation products in cryoprotected and frozen rice cells: consequences for post-thaw survival , 1992 .

[19]  F. Navari-Izzo,et al.  Degradation of membrane lipid components and antiovidanl levels in Hordeum vulgare exposed to long-term fumigation with SO2 , 1992 .

[20]  L. Snee,et al.  40Ar/39Ar systematics and argon diffusion in amber: implications for ancient earth atmospheres , 1991 .

[21]  J. Raven Plant responses to high O2 concentrations: relevance to previous high O2 episodes , 1991 .

[22]  W. Horst,et al.  Effect of aluminium on lipid peroxidation, superoxide dismutase, catalase, and peroxidase activities in root tips of soybean (Glycine max) , 1991 .

[23]  A. Price,et al.  The role of ascorbate in drought-treated Cochlearia atlantica Pobed. and Armeria maritima (Mill.) Willd. , 1991, New Phytologist.

[24]  L. Langeberg,et al.  Effects of ambient oxygen and of fixed nitrogen on concentrations of glutathione, ascrobate, and associated enzymes in soybean root nodules. , 1991, Plant physiology.

[25]  J. Tallis,et al.  Plant Community History. , 1991 .

[26]  S. Pukacka Changes in membrane lipid components and antioxidant levels during natural ageing of seeds of Acer platanoides , 1991 .

[27]  A. Price,et al.  Iron‐catalysed oxygen radical formation and its possible contribution to drought damage in nine native grasses and three cereals , 1991 .

[28]  Robert A. Berner,et al.  A model for atmospheric CO 2 over Phanerozoic time , 1991 .

[29]  S. Parkin Plant lipid biochemistry, structure and utilization; Edited by P J Quinn and J L Harwood. pp 483. Portland Press, London. 1991. £47.50 ISBN 1-85578-003-8 , 1991 .

[30]  M. Macaulay,et al.  Superoxide Dismutase and Susceptibility Of Potato (Solanum tuberosum L.) Tubers To Calcium Related Disorders , 1991 .

[31]  L. A. Del Río,et al.  Nutritional effect and expression of SODs: induction and gene expression; diagnostics; prospective protection against oxygen toxicity. , 1991, Free radical research communications.

[32]  P. Thorpe,et al.  THE ROLE OF FREE RADICALS AND RADICAL PROCESSING SYSTEMS IN LOSS OF DESICCATION TOLERANCE IN GERMINATING MAIZE (ZEA MAYS L.) , 1990 .

[33]  A. Wellburn,et al.  Electron spin resonance evidence for the formation of free radicals in plants exposed to ozone , 1990 .

[34]  A. Price,et al.  Role of Iron in Chlorophyll Destruction in Stressed Plants , 1990 .

[35]  J. Houghton,et al.  Botanical and microbiological aspects of porphyrins , 1990 .

[36]  A. Price A possible role for calcium in oxidative plant stress. , 1990, Free radical research communications.

[37]  R. Crawford,et al.  Studies in Plant Survival. , 1989 .

[38]  W. Ernst,et al.  Copper-induced Damage to the Permeability Barrier in Roots of Silene cucubalus , 1989 .

[39]  Jennifer M. Robinson,et al.  Phanerozoic O2 variation, fire, and terrestrial ecology , 1989 .

[40]  X. Gidrol,et al.  Biochemical changes induced by accelerated aging in sunflower seeds. I. Lipid peroxidation and membrane damage , 1989 .

[41]  A. Paulin,et al.  Changes in activities of superoxide dismutases during aging of petals of cut carnations (Dianthus caryophyllus) , 1989 .

[42]  H. Marschner,et al.  High Light Intensity Enhances Chlorosis and Necrosis in Leaves of Zinc, Potassium, and Magnesium Deficient Bean (Phaseolus vulgaris) Plants , 1989 .

[43]  P. Low,et al.  Rapid Stimulation of an Oxidative Burst during Elicitation of Cultured Plant Cells : Role in Defense and Signal Transduction. , 1989, Plant physiology.

[44]  D. Canfield,et al.  A new model for atmospheric oxygen over Phanerozoic time. , 1989, American journal of science.

[45]  Stanley B. Brown,et al.  THE DEGRADATION OF CHLOROPHYLL - A BIOLOGICAL ENIGMA. , 1987, The New phytologist.

[46]  G. Hendrỳ,et al.  IRON-INDUCED OXYGEN RADICAL METABOLISM IN WATERLOGGED PLANTS. , 1985, The New phytologist.

[47]  B. Halliwell,et al.  Free radicals in biology and medicine , 1985 .

[48]  D. Rea,et al.  Geologic Approach to the Long-Term History of Atmospheric Circulation , 1985, Science.

[49]  L. Hickey Land plant evidence compatible with gradual, not catastrophic, change at the end of the Cretaceous , 1981, Nature.

[50]  L. Frakes Climates Throughout Geologic Time , 1979 .

[51]  E. M. Kemp,et al.  Influence of Continental Positions on Early Tertiary Climates , 1972, Nature.