Canadian Forest Service Publications

Shoot water relations of mature black spruce families displaying a genotype x environment interaction in growth rate. III. Diurnal patterns as influenced by vapor pressure deficit and internal water status. 2001. Major, J.E.; Johnsen, K.H. Tree Physiology 21: 579-587.

Year: 2001

Issued by: Atlantic Forestry Centre

Catalog ID: 18290

Language: English

Availability: Order paper copy (free)

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Pressure-volume curves were constructed and shoot water potentials measured for +20-year-old black spruce (Picea mariana (Mill.) BSP) trees from four full-sib families growing on a moist site and a dry site at the Petawawa Research Forest, Ontario, to determine whether differences in diurnal water relations traits were related to productivity. To assess the basis for the observed diurnal patters, we analyzed effects of environmental and internal water stress variables on diurnal water relations traits. Among the water relations traits examined, turgor pressure was the most sensitive, responding to site, family and environmental variables and displaying the strongest diurnal responses to varying soil water availability and atmospheric vapor pressure deficit (VPD). Overall, there was an 84% drop in turgor pressure with increasing VPD: turgor pressure fell 46% in response to the first 0.75 kPa increase in VPD, and 9.7% in response to a second 0.75 kPa increase in VPD. The families differed in water relations responses to moderate water stress, but not in responses to minor or more extreme water stresses. Thus, at a VPD of 0.5 kPa, there was an estimated 83% greater family difference in turgor pressure on the dry site compared with the moist site. Soil and atmospheric water stress appeared to exert effects in tandem to elicit these responses (r2 = 0.728). A comparison of the mechanisms of response to water deficit indicated that osmotic adjustment was more important than change in cell wall elasticity. We used a conceptual water relations model to illustrate the differences between tolerant and intolerant families in their mechanisms of water stress response. We conclude that, because genetic responses to site factors are dynamic, the integrated response over time contributes to the observed genetic X environmental interaction in growth.