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Stomatal regulation in Douglas fir following a fungal-mediated chronic reduction in leaf area

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Abstract

Pathogens can cause chronic premature needle abscission in coniferous species. To assess the potential impacts on tree productivity, stomatal regulation was investigated in Douglas fir with chronic stomatal occlusion and defoliation from varying levels of the Swiss needle cast (SNC) fungus, Phaeocryptopus gaeumannii. Levels of SNC disease and subsequent defoliation were manipulated by choosing six sites with varying levels of disease and by foliar applications of fungicides on six trees per site. Diurnal measurements of leaf water potential (Ψleaf), stomatal conductance (g s) and vapor pressure deficit (D) were made on six fungicide treated and six control trees per site. In addition, leaf specific hydraulic conductance was calculated on a single branch (K L_B) from three trees per treatment per site. Stomatal conductance at D=1 kPa (g sref) was negatively correlated with fungal colonization (number of fruiting bodies present in needle stomata) and positively correlated with K L_B. Despite reduced needle retention in diseased trees, K L declined due to a reduction in sapwood area and permeability (i.e., increasing presence of latewood in functional sapwood). In general, stomatal sensitivity to D for all foliage was consistent with stomatal regulation based on a simple hydraulic model [g s=K Lsoil−Ψleaf)/ D], which assumes strict stomatal regulation of Ψleaf. However, when fungal presence reduced maximum g s below the potential maximum supported by hydraulic architecture, stomatal sensitivity was lower than expected based on the theoretical relationship: dg s/dlnD=0.6·g sref. The results indicate that losses in productivity associated with physical blockage of stomata and defoliation are compounded by additional losses in K L and a reduction in g s in remaining functional stomata.

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References

  • Bond BJ, Kavanagh KL (1999) Stomatal behavior of four woody species in relation to leaf-specific hydraulic conductance and threshold water potential. Tree Physiol 19:503–510

    PubMed  Google Scholar 

  • Capitano B (1999) The infection and colonization of Douglas-fir by P. gaeumannii. MS thesis, Oregon State University, Corvallis

  • Day ME, Greenwood MS, White AS (2001) Age-related changes in foliar morphology and physiology in red spruce and their influence on declining photosynthetic rates and productivity with tree age. Tree Physiol 21:1195–1204

    CAS  PubMed  Google Scholar 

  • Dewar R.C (1995) Interpretation of an empirical model for stomatal conductance in terms of guard cell function. Plant Cell Environ 18:365–372

    Google Scholar 

  • Hansen EM, Lewis KJ (1997) Compendium of conifer diseases. APS, St. Paul, Minn.

  • Hansen EM, Stone JK, Capitano BR, Rosso P, Sutton W, Winton L, Kanaskie A, McWilliams MG (2000) Incidence and impacts of Swiss needle cast in forest plantations of Douglas-fir in coastal Oregon. Plant Dis 84:773–778

    Google Scholar 

  • Harley PC, Thomas RB, Reynolds JF Strain BR (1992) Modeling photosynthesis of cotton grown in elevated CO2. Plant Cell Environ 15:271–282

    Google Scholar 

  • Hubbard RM, Ryan MG, Stiller V, Sperry JS (2001) Stomatal conductance and photosynthesis vary linearly with plant hydraulic conductance in ponderosa pine. Plant Cell Environ 24:113–121

    Article  Google Scholar 

  • Jones HG (1990) Physiological aspects of the control of water status in horticultural crops. Hortic Sci 25:19–26

    Google Scholar 

  • Jones HG (1992) Plants and microclimate, 2nd edn. Cambridge University Press, Cambridge

  • Jones HG, Sutherland RA (1991) Stomatal control of xylem embolism. Plant Cell Environ 14:607–612

    Google Scholar 

  • Kavanagh KL, Bond BJ, Aitken SN, Gartner BL, Knowe S (1999) Shoot and root vulnerability to xylem cavitation in four populations of Douglas-fir seedlings. Tree Physiol 19:31–37

    PubMed  Google Scholar 

  • Kramer PJ, Boyer JS (1995) Water relations of plants and soils. Academic Press, San Diego

  • Manter DK, Bond BJ, Kavanagh KL, Rosso PH, Filip GM (2000) Timing and mechanism of impact of the Swiss needle cast fungus, Phaeocryptopus gaeumannii, on Douglas-fir needle gas exchange and rubisco activation. New Phytol 148:481–491

    CAS  Google Scholar 

  • Manter DK, Bond BJ, Kavanagh KL, Stone JK, Filip GM (2003) Modelling the impacts of the foliar pathogen, Phaeocryptopus gaeumannii, on Douglas fir physiology: net canopy carbon assimilation, needle abscission and growth. Ecol Model (in press)

    Google Scholar 

  • McNaughton KG, Jarvis PG (1991) Effects of spatial scale on stomatal control of transpiration. Agric For Meteorol 54:279–301

    Google Scholar 

  • Megraw RA (1986) Douglas-fir wood properties. In: Oliver CD, Hanley DP, Johnson JA (eds) Douglas-fir: stand management for the future. University of Washington, Institute of Forest Resources, Contribution No. 55, Seattle, pp 81–96

  • Meinzer FC, Grantz DA (1990) Stomatal and hydraulic conductance in growing sugarcane: stomatal adjustment to water transport capacity. Plant Cell Environ 13:383–388

    Google Scholar 

  • Monteith JL (1995) A reinterpretation of stomatal response to humidity. Plant Cell Environ 18:357–364

    Google Scholar 

  • Oren R, Sperry JS, Katul GG, Pataki DE, Ewers BE, Phillips N (1999) Intra- and interspecific responses of canopy stomatal conductance to vapour pressure deficit. Plant Cell Environ 22:1515–1526

    Article  Google Scholar 

  • Oren R, Sperry J, Ewers B, Pataki D, Phillips N, Megonigal J (2001) Sensitivity of mean canopy stomatal conductance to vapor pressure deficit in a flooded Taxodium distichum L. forest: hydraulic and non-hydraulic effects. Oecologia 126:21–29

    Article  Google Scholar 

  • Pataki DE, Oren R, Phillips N (1998) Responses of sap flux and stomatal conductance of Pinus taeda L. trees to stepwise reductions in leaf area. J Exp Bot 49:871–878

    CAS  Google Scholar 

  • Reich PB, Walters MB, Krause SC, Vanderlien DW, Raffa KF Tabone T (1993) Influence of pre-dawn water potential and soil-to-leaf hydraulic conductance on maximum daily leaf diffusive conductance in two oak species. Funct Ecol 3:719–726

    Google Scholar 

  • Ryan M, Yoder B (1997) Hydraulic limits to tree height and tree growth. BioScience 47:235–242

    Google Scholar 

  • Saliendra, NZ, Sperry JS, Comstock MP (1995) Influences of leaf water status on stomatal response to humidity, hydraulic conductance, and soil drought in Betula occidentalis. Planta 196:356–366

    Google Scholar 

  • Schäfer KVR, Oren R, Tenhunen JD (2000) The effect of tree height on crown level stomatal conductance. Plant Cell Environ 23:365–375

    Google Scholar 

  • Sperry JS, Pockman WT (1993) Limitation of transpiration by hydraulic conductance and xylem cavitation in Betula occidentalis. Plant Cell Environ 16:279–287

    Google Scholar 

  • Tausend PC, Meinzer FC, Goldstein G (2000) Control of transpiration in three coffee cultivars: the role of hydraulic and crown architecture. Trees 14:181–190

    Google Scholar 

  • Tezara W, Mitchell VJ, Driscoll SD, Lawlor DW (1999) Water stress inhibits plant photosynthesis by decreasing coupling factor and ATP. Nature 401:914–917

    Google Scholar 

  • Whitehead D (1998) Regulation of stomatal conductance and transpiration in forest canopies. Tree Physiol 18:633–644

    PubMed  Google Scholar 

  • Williams M, Rasletter EB, Fernandes DN, Goulden ML, Wofsy SC, Shaver GR, Melillo JM, Munger JW, Fan S-M, Nadelhoffer KJ (1996) Modeling the soil-plant-atmosphere continuum in a QuercusAcer stand at Harvard Forest: the regulation of stomatal conductance by light, nitrogen and soil/plant hydraulic properties. Plant Cell Environ 19:911–927

    Google Scholar 

  • Zimmerman MH (1983) Xylem structure and the ascent of sap. Springer, Berlin Heidelberg New York

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Acknowledgements

We are grateful to Dr. Barbara Bond for the loan of several LiCor gas exchange analyzers. This research was funded through the Swiss Needle Cast Cooperative at Oregon State University—a consortium of industrial, tribal, federal, and state landowners in Oregon and Washington.

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Correspondence to Daniel K. Manter.

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Manter, D.K., Kavanagh, K.L. Stomatal regulation in Douglas fir following a fungal-mediated chronic reduction in leaf area. Trees 17, 485–491 (2003). https://doi.org/10.1007/s00468-003-0262-2

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