Literature DB >> 15355865

The management of extracellular ice by petioles of frost-resistant herbaceous plants.

M E McCully1, M J Canny, C X Huang.   

Abstract

BACKGROUND AND AIMS: Some frost-tolerant herbaceous plants droop and wilt during frost events and recover turgor and posture on thawing. It has long been known that when plant tissues freeze, extracellular ice forms. Distributions of ice and water in frost-frozen and recovered petioles of Trifolium repens and Escholschzia californica were visualized.
METHODS: Petioles of intact plants were cryo-fixed, planed to smooth transverse faces, and examined in a cryo-SEM. KEY
RESULTS: With frost-freezing, parenchyma tissues shrank to approx. one-third of their natural volume with marked cytorrhysis of the cells, and massive blocks of extracellular icicles grew under the epidermis (poppy) or epidermis and subepidermis (clover), leaving these layers intact but widely separated from the parenchyma except at specially structured anchorages overlying vascular bundles. On thawing, the extracellular ice was reabsorbed by the expanding parenchyma, and surface tissues again contacted the internal tissues at weak junctions (termed faults). These movements of water into and from the fault zones occurred repeatedly at each frost/thaw event, and are interpreted to explain the turgor changes that led to wilting and recovery. Ice accumulations at tri-cellular junctions with intercellular spaces distended these spaces into large cylinders, especially large in clover. Xylem vessels of frozen petioles were nearly all free of gas; in thawed petioles up to 20 % of vessels were gas-filled.
CONCLUSIONS: The occurrence of faults and anchorages may be expected to be widespread in frost-tolerant herbaceous plants, as a strategy accommodating extracellular ice deposits which prevent intracellular freezing and consequent membrane disruption, as well as preventing gross structural damage to the organs. The developmental processes that lead to this differentiation of separation of sheets of cells firmly cemented at determined regions at their edges, and their physiological consequences, will repay detailed investigation.

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Year:  2004        PMID: 15355865      PMCID: PMC4242212          DOI: 10.1093/aob/mch191

Source DB:  PubMed          Journal:  Ann Bot        ISSN: 0305-7364            Impact factor:   4.357


  6 in total

1.  The reliability of cryoSEM for the observation and quantification of xylem embolisms and quantitative analysis of xylem sap in situ.

Authors:  M E McCully; M W Shane; A N Baker; C X Huang; L E Ling; M J Canny
Journal:  J Microsc       Date:  2000-04       Impact factor: 1.758

2.  Equilibrium freezing of leaf water and extracellular ice formation in Afroalpine 'giant rosette' plants.

Authors:  E Beck; E D Schulze; M Senser; R Scheibe
Journal:  Planta       Date:  1984-09       Impact factor: 4.116

3.  Extracellular ice and cell shape in frost-stressed cereal leaves: A low-temperature scanning-electron-microscopy study.

Authors:  R S Pearce
Journal:  Planta       Date:  1988-09       Impact factor: 4.116

4.  Cell shape and localisation of ice in leaves of overwintering wheat during frost stress in the field.

Authors:  R S Pearce; E N Ashworth
Journal:  Planta       Date:  1992-10       Impact factor: 4.116

5.  The Formation and Distribution of Ice within Forsythia Flower Buds.

Authors:  E N Ashworth
Journal:  Plant Physiol       Date:  1990-03       Impact factor: 8.340

6.  Water Relations of Pachysandra Leaves during Freezing and Thawing : Evidence for a Negative Pressure Potential Alleviating Freeze-Dehydration Stress.

Authors:  J J Zhu; E Beck
Journal:  Plant Physiol       Date:  1991-11       Impact factor: 8.340

  6 in total
  10 in total

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Journal:  PhytoKeys       Date:  2016-06-13       Impact factor: 1.635

2.  Photosynthesis at an extreme end of the leaf trait spectrum: how does it relate to high leaf dry mass per area and associated structural parameters?

Authors:  Foteini Hassiotou; Michael Renton; Martha Ludwig; John R Evans; Erik J Veneklaas
Journal:  J Exp Bot       Date:  2010-05-19       Impact factor: 6.992

3.  Ice accommodation in plant tissues pinpointed by cryo-microscopy in reflected-polarised-light.

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4.  Deep supercooling enabled by surface impregnation with lipophilic substances explains the survival of overwintering buds at extreme freezing.

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5.  The cold-stress responsive gene DREB1A involved in low-temperature tolerance in Xinjiang wild walnut.

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Journal:  PeerJ       Date:  2022-09-08       Impact factor: 3.061

6.  Physiological and molecular mechanisms of the response of roots of Pinus massoniana Lamb. to low-temperature stress.

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Review 7.  Cold Hardiness in Trees: A Mini-Review.

Authors:  Michael Wisniewski; Annette Nassuth; Rajeev Arora
Journal:  Front Plant Sci       Date:  2018-09-20       Impact factor: 5.753

8.  MUR1-mediated cell-wall fucosylation is required for freezing tolerance in Arabidopsis thaliana.

Authors:  Paige E Panter; Olivia Kent; Maeve Dale; Sarah J Smith; Mark Skipsey; Glenn Thorlby; Ian Cummins; Nathan Ramsay; Rifat A Begum; Dayan Sanhueza; Stephen C Fry; Marc R Knight; Heather Knight
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Review 9.  Responses of the Plant Cell Wall to Sub-Zero Temperatures: A Brief Update.

Authors:  Daisuke Takahashi; Ian R Willick; Jun Kasuga; David P Livingston Iii
Journal:  Plant Cell Physiol       Date:  2021-12-27       Impact factor: 4.927

10.  Winter Nights during Summer Time: Stress Physiological Response to Ice and the Facilitation of Freezing Cytorrhysis by Elastic Cell Wall Components in the Leaves of a Nival Species.

Authors:  Matthias Stegner; Barbara Lackner; Tanja Schäfernolte; Othmar Buchner; Nannan Xiao; Notburga Gierlinger; Andreas Holzinger; Gilbert Neuner
Journal:  Int J Mol Sci       Date:  2020-09-24       Impact factor: 6.208

  10 in total

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