“…A number of studies on woody plants have implied that Similarly, the symplastic water fi'action, the relative changes in cold hardiness and tissue water relations pa-water content at the turgor loss point, water potential at ratneters may be related (Tyree et al, 1978, Roberts et al, the turgor loss point, and osmotic potential decrease dtjr-1980, Ritchie and Shula 1984, Teskey et al, 1984, Doi et mg cold acclimation and later increase during deacclimaal, 1986Gross and Koch 1991Grossnickie 1992, Tis-tion (Roberts andKnoerr 1977, Tyree et al, 1978, Roberts sue water content has been observed to decrease m vari-et al, 1980, Ritchie and Shula 1984, Teskey et al, 1984, ous species during cold .acclimation (Roberts and Knoen-Doi et al, 1986, Auge and Stodola 1989, Grossnickie 1977Bray and Parsons 1981Grossnickie 1992, The 1992), In contrast, the maximum bulk modules of elasftcwater loss observed during cold acclimation may be only ity increases during cold acchmation and decreases durapparent water loss as the result of dry matter accumula-tng deacdimation in the spnng (Ritchie and Simla 1984, Auge and Stodola 1989, Grossnickie 1992, These changes parallel those obsei-ved in woody plants subjected to drought (Bongarten atid Teskey 1986, Abrams 1988, Parker and Pallardy 1988, Zwiazek 1991, Increased cold hardiness induced by water stress has been reported for many plants (Chen and Li 1977, Yelenosky 1979, Biddington and Dearman 1988, Anisko and Lindstrom 1995, Mechanisms proposed to explain the water-stress-induced increases in cold hardiness include either the removal of nonessentia! water which could participate in mechanically damaging crystallization during freezing (Li and Weiser 1971) or the depression of the freezing temperature which is associated with a decline in osmotic potential (Li and Weiser 1971…”