Oxygen deprivation stress in a changing environment

Past research into flooding tolerance and oxygen shortages in plants has been motivated largely by cultivation problems of arable crops. Unfortunately, such species are unsuitable for investigating the physiological and biochemical basis of anoxia-tolerance as selection has reduced any tolerance of anaerobiosis and anaerobic soil conditions that their wild ancestors might have possessed, Restoration of anoxia-tolerance to species that have lost this property is served better by physiological and molecular studies of the mechanisms that are employed in wild species that still possess long-term anoxia-tolerance. Case studies developing these arguments are presented in relation to a selection of crop and wild species, The flooding sensitivity and metabolism of maize is compared in relation to rice in its capacity for anaerobic germination, The sensitivity of potato to flooding is related to its disturbed energy metabolism and inability to maintain functioning membranes under anoxia and post-inoxia, By contrast, long-term anoxia-tolerance in the American cranberry (Vaccinium macrocarpon) and the arctic grass species Deschampsia beringensis can be related to the provision and utilization of carbohydrate reserves. Among temperate species, the sweet flag (Acorus calamus) shows a remarkable tolerance of anoxia in both shoots and roots and is also able to mobilize carbohydrate and maintain ATP levels during anoxia as well as preserving membrane lipids against anoxic and post-anoxic injury. Phragmites australis and Spartina alterniflora, although anoxia-tolerant, are both sulphide-sensitive species which can pre-dispose them to the phenomenon of die-back in stagnant, nutrient-rich water. Glyceria maxima adapts to flooding through phenological adaptations with a seasonal metabolic tolerance of anoxia confined to winter and spring which, combined with a facility for root aeration and early spring growth, allows rapid colonization of sites with only shallow flooding. The diversity of responses to flooding in wild plants suggests that, depending on the life strategy and habitat of the species, many different mechanisms may be involved in adapting plants to survive periods of inundation and no one mechanism on its own is adequate for ensuring survival.

[1]  M. Sachs,et al.  Anaerobic tolerant null: a mutant that allows Adh1 nulls to survive anaerobic treatment. , 1989, The Journal of heredity.

[2]  J. Bongaarts,et al.  Climate Change: The IPCC Scientific Assessment. , 1992 .

[3]  B. Gudleifsson Metabolic and Cellular Impact of Ice Encasement on Herbage Plants , 1993 .

[4]  R. Brändle,et al.  Amino Acid Composition in Rhizomes of Wetland Species in Their Natural Habitat and under Anoxia , 1988 .

[5]  R. Brändle,et al.  Aspects of plant behaviour under anoxia and post-anoxia , 1994 .

[6]  R. Brändle,et al.  Ethanol, acetaldehyde, ethylene release and ACC concentration of rhizomes from marsh plants under normoxia, hypoxia and anoxia , 1987 .

[7]  V. Walbot,et al.  Cytoplasmic acidosis as a determinant of flooding intolerance in plants. , 1984, Proceedings of the National Academy of Sciences of the United States of America.

[8]  J. Pretorius,et al.  The effect of soaking injury in bean seeds on protein synthesis in embryonic axes , 1991, Seed Science Research.

[9]  C. Kuhlemeier,et al.  Long-Term Anoxia Tolerance (Multi-Level Regulation of Gene Expression in the Amphibious Plant Acorus calamus L.) , 1993, Plant physiology.

[10]  F. Fox Ascorbic-acid metabolism. , 1947, Lancet.

[11]  T. Vantoai,et al.  Postanoxic Injury in Soybean (Glycine max) Seedlings. , 1991, Plant physiology.

[12]  H. Tsuji,et al.  Development of the O2--Detoxification System during Adaptation to Air of Submerged Rice Seedlings , 1992 .

[13]  M. Jackson,et al.  An examination of the importance of ethanol in causing injury to flooded plants , 1982 .

[14]  H. Končalová Anatomical adaptations to waterlogging in roots of wetland graminoids: limitations and drawbacks , 1990 .

[15]  M. Jackson,et al.  Mechanisms of flood tolerance in plants , 1994 .

[16]  R. Delaune,et al.  Sulfide-induced toxicity: inhibition of carbon assimilation in Spartina alterniflora , 1988 .

[17]  R. Brändle Flooding Resistance of Rhizomatous Amphibious Plants , 1991 .

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

[19]  Wolfgang Ostendorp,et al.  Schilf als Lebensraum , 1993 .

[20]  R. Crawford Plant life in aquatic and amphibious habitats , 1987 .

[21]  I. Mendelssohn,et al.  Sulphide as a soil phytotoxin: differential responses in two marsh species , 1989 .

[22]  R. Crawford,et al.  Superoxide Dismutase as an Anaerobic Polypeptide : A Key Factor in Recovery from Oxygen Deprivation in Iris pseudacorus? , 1987, Plant physiology.

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

[24]  P. Eck American Cranberry , 1990, Summer Wildflowers of the Northeast.

[25]  A. Lane,et al.  Relationships between the rate of synthesis of ATP and the concentrations of reactants and products of ATP hydrolysis in maize root tips, determined by 31P nuclear magnetic resonance. , 1985, Archives of biochemistry and biophysics.

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

[27]  R. Crawford,et al.  Enzymatic defence against post-anoxic injury in higher plants , 1994 .

[28]  R. Alscher Biosynthesis and antioxidant function of glutathione in plants , 1989 .

[29]  P. Perata,et al.  Plant responses to anaerobiosis , 1993 .

[30]  R. Crawford,et al.  Similarities between post-ischaemic injury to animal tissues and post-anoxic injury in plants , 1994 .

[31]  W. Armstrong,et al.  Phragmites australis: Venturi- and humidity-induced pressure flows enhance rhizome aeration and rhizosphere oxidation , 1992 .

[32]  G. Albrecht,et al.  Protection against activated oxygen following re-aeration of hypoxically pretreated wheat roots. The response of the glutathione system , 1994 .

[33]  B. Gudleifsson Metabolite accumulation during ice encasement of timothy grass ( Phleum pratense L.) , 1994 .

[34]  T. Kozlowski Flooding and Plant Growth , 1985 .

[35]  R. Brändle,et al.  Energy Metabolism in Rhizomes of Acorus calamus (L.) and in Tubers of Solanum tuberosum (L.) With Regard to their Anoxia Tolerance , 1991 .

[36]  T. Henzi,et al.  Long Term Survival of Rhizomatous Species Under Oxygen Deprivation , 1993 .

[37]  R. Larson The antioxidants of higher plants , 1988 .

[38]  L. Christersson,et al.  Advances in Plant Cold Hardiness , 1993 .

[39]  E. Elstner,et al.  Mechanisms of oxygen activation during plant stress , 1994 .

[40]  S. Matthews,et al.  The Damaging Effect of Water on Dry Pea Embryos During Imbibition , 1978 .

[41]  W. Grosse,et al.  Pressurized ventilation in wetland plants , 1991 .

[42]  I. Anderson,et al.  Further Evidence that Cytoplasmic Acidosis Is a Determinant of Flooding Intolerance in Plants. , 1985, Plant physiology.

[43]  R. Crawford,et al.  Anoxia Tolerance in High Arctic Vegetation , 1994 .

[44]  R. Crawford Oxygen availability as an ecological limit to plant distribution , 1992 .

[45]  H. Brix GAS EXCHANGE THROUGH DEAD CULMS OF REED, PHRAGMITES AUSTRALIS (CAV.) TRIN. EX STEUDEL , 1989 .

[46]  R. Crawford,et al.  The Effect of Anaerobiosis on Carbohydrate Levels in Storage Tissues of Wetland Plants , 1983 .

[47]  R. Crawford,et al.  Rhizome anoxia tolerance and habitat specialization in wetland plants , 1987 .

[48]  I. Mendelssohn,et al.  Mechanism for the hydrogen sulfide‐induced growth limitation in wetland macrophytes , 1990 .