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Freeze–thaw cycles (FTCs) are the major seasonal environment stress in the temperate and boreal forests, which induces hydraulic dysfunction and limits tree growth and distribution. There are two types of FTCs in the field: FTCs with increasing temperature from winter to spring (spring FTCs); and FTCs with decreasing temperature from autumn to winter (autumn FTCs). While previous studies have evaluated the hydraulic function during the growing season, its seasonal changes and how it adapts to different types of FTCs remain unverified. To fill this knowledge gap, the eight tree species from three wood types (ring- and diffuse-porous, tracheid) were selected in a temperate forest undergoing seasonal FTCs. We measured the branch hydraulic traits in spring, summer, autumn, and early, middle, and late winter. Ring-porous trees always showed low native hydraulic conductance (Kbranch), and high percentage loss of maximum Kbranch (PLCB) and water potential that loss of 50% maximum Kbranch (P50B) in non-growing seasons (except summer). Kbranch decreased, and PLCB and P50B increased in diffuse-porous trees after several spring FTCs. In tracheid trees, Kbranch decreased after spring FTCs while the P50B did not change. All sampled trees gradually recovered their hydraulic functions from spring to summer. Kbranch, PLCB, and P50B of diffuse-porous and tracheid trees were relatively constant after autumn FTCs, indicating almost no effect of autumn FTCs on hydraulic functions. These results suggested that hydraulic functions of temperate trees showed significant seasonal changes, and spring FTCs induced more hydraulic damage (except ring-porous trees) than autumn FTCs, which should be determined by the number of FTCs and trees’ vitality before FTCs. These findings advance our understanding of seasonal changes in hydraulic functions and how they cope with different types of freeze–thaw cycles in temperate forests.
Freeze–thaw cycles (FTCs) are the major seasonal environment stress in the temperate and boreal forests, which induces hydraulic dysfunction and limits tree growth and distribution. There are two types of FTCs in the field: FTCs with increasing temperature from winter to spring (spring FTCs); and FTCs with decreasing temperature from autumn to winter (autumn FTCs). While previous studies have evaluated the hydraulic function during the growing season, its seasonal changes and how it adapts to different types of FTCs remain unverified. To fill this knowledge gap, the eight tree species from three wood types (ring- and diffuse-porous, tracheid) were selected in a temperate forest undergoing seasonal FTCs. We measured the branch hydraulic traits in spring, summer, autumn, and early, middle, and late winter. Ring-porous trees always showed low native hydraulic conductance (Kbranch), and high percentage loss of maximum Kbranch (PLCB) and water potential that loss of 50% maximum Kbranch (P50B) in non-growing seasons (except summer). Kbranch decreased, and PLCB and P50B increased in diffuse-porous trees after several spring FTCs. In tracheid trees, Kbranch decreased after spring FTCs while the P50B did not change. All sampled trees gradually recovered their hydraulic functions from spring to summer. Kbranch, PLCB, and P50B of diffuse-porous and tracheid trees were relatively constant after autumn FTCs, indicating almost no effect of autumn FTCs on hydraulic functions. These results suggested that hydraulic functions of temperate trees showed significant seasonal changes, and spring FTCs induced more hydraulic damage (except ring-porous trees) than autumn FTCs, which should be determined by the number of FTCs and trees’ vitality before FTCs. These findings advance our understanding of seasonal changes in hydraulic functions and how they cope with different types of freeze–thaw cycles in temperate forests.
Spring freezing is an unforgiving stress for young leaves, often leading to death, with consequences for tree productivity and survival. While both the plant water transport system and living tissues are vulnerable to freezing, we do not know whether damage to one or both of these systems causes death in young leaves exposed to unseasonal freezing. Whole saplings of Liriodendron tulipifera were exposed to freezing and thawing trajectories designed to mimic spring freezes in nature. We visualised freezing damage to the water transport system (xylem embolism) and living tissues (mesophyll freezing, decline in chlorophyll fluorescence). We 1.) provide the first visualisation of freeze-thaw embolism in leaves, 2.) reveal a predictable progression of ice formation within the mesophyll which is strongly influenced by leaf vein architecture, notably the presence or absence of bundle sheath extensions, and 3.) show that freeze-thaw embolism occurs only in the largest vein orders where mean vessel diameter exceeds 30 microns. With evidence of both freeze-thaw embolism and damage to photosynthetic tissue, we conclude that this dual-mode lethality may be common among other wide-vesseled angiosperm-leaves, potentially playing a role in limiting distributions, and show that bundle sheath extensions may stall or even prevent freezing spread.
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