Abstract
Plant-dry-matter accumulation ultimately depends on the yield of carbon building blocks (i.e., nonstructural carbohydrates) from the difference between carbon assimilation (Chapter 3, this volume) and autotrophic respiration (Chapter 4, this volume). Accumulated sugar and starch reserves in roots and shoots (Chapter 5, this volume) represent the primary compounds, along with stored elements, that must be present to support mass accumulation in the stems of saplings and trees. Waring and Pitman (1985) proposed a hierarchy of photosynthate allocation priorities for trees that considers stem growth to be a relatively low allocation priority, suggesting that changes in stem-growth rates would be a sensitive indicator of water stress response. Sustained low stem-growth rates have also been linked to mortality (Kohyama and Hara 1989; Pedersen 1998; Swaine et al. 1987; Tainter et al. 1984). Because growth and mortality are the integrated result of of physiological responses to environmental stress, they represent key end points for investigations of forest response to changing precipitation regimes. This chapter describes the annual growth and mortality of saplings and large trees during 7 full years of throughfall manipulation (1994–2000) and provides a quantitative description of the response of tree growth to soil-water deficits. The Throughfall Displacement Experiment (TDE) observations are also contrasted with published data for other deciduous hardwood forests, and their application for predicting growth responses to soil-water deficits throughout the eastern deciduous hardwood forest is discussed.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Preview
Unable to display preview. Download preview PDF.
References
Abrams MD (1990) Adaptations and responses to drought in Quercus species of North America. Tree Physiol 7: 227–238.
Abrams MD, Ruffner CM, Morgan TA (1998) Tree-ring responses to drought across species and contrasting sites in the ridge and valley of central Pennsylvania. For Sci 44:550–558.
Bahari ZA, Pallardy SG, Parker WC (1985) Photosynthesis, water relations, and drought adaptation in six woody species of oak-hickory forests in central Missouri. For Sci 31:557–569.
Brady NC (1974) The Nature and Property of Soils (8th Edition). MacMillan Publishing Company, New York, pp. 190–192.
Borchert R (1998) Responses of tropical trees to rainfall seasonality and its long term changes. Clim Change 39: 381–393.
Bréda N, Cochard H, Dreyer E, Granier A (1993) Water transfer in a mature oak stand (Quercus petraea): Seasonal evolution and effects of a severe drought. Can J For Res 23:1136–1143.
Bréda N, Granier A (1996) Intra-and interannual variations of transpiration, leaf area index and radial growth of a sessile oak stand (Quercus petraea). Ann Sci For 53:521–536.
Buell MF, Buell HF, Small JA, Monk CD (1961) Drought effect on radial growth of trees in the William L. Hutcheson Memorial Forest. Bull Torrey Bot Club 88:176–180.
Burns DP, Gibson LP (1968) The leaf-mining weevil of yellow-poplar. Can Entomol 100:421–429.
Edwards NT, Hanson PJ (1996) Stem respiration in a closed-canopy upland oak forest. Tree Physiol 16:433–439.
Elliott J, Anderson P, Davis GR, Wong FSL, Dover SD (1994) Computed tomography Part II: The practical use of a single-source and detector. JOMJ Min Met Mat Soc 46:11–19.
Ellsworth DS, Reich PB (1992) Water relations and gas exchange of Acer saccharum seedlings in contrasting natural light and water regimes. Tree Physiol 10:1–20.
Epron D, Dreyer E (1993) Long-term effects of drought on photosynthesis of adult oak trees [Quercus petraea (Matt.) Liebl. and Quercus robur L.] in a natural stand. New Phytol 125:381–389.
Fritts HC (1960) Multiple regression analysis of radial growth in individual trees. For Sci 6:334–349.
Fritts HC (1962) The relation of growth ring widths in American beech and white oak to variations in climate. Tree-Ring Bull 25:2–10.
Gebre GM, Tschaplinski TJ, Shirshac TL (1998) Response in water relations of several hardwood species to through-fall manipulation in an upland oak forest during a wet year. Tree Physiol 18:299–305.
Haasis RW (1934) Diametrical changes in tree trunks. Publication No. 450. Carnegie Institution of Washington, Washington, District of Columbia.
Hanson PJ, Weltzin JF (2000) Drought disturbance from climate change: Response of United States forests. Science Total Environ 262:205–220.
Hanson PJ, Todd DE, Amthor JS (2001a) A six year study of sapling and large-tree growth and mortality responses to natural and induced variability in precipitation and throughfall. Tree Physiol 21:345–358.
Hanson PJ, Todd DE, Riggs JS, Wolfe ME, O’Neill EG (2001b) Walker Branch Throughfall Displacement Experiment data report: Site characterization, system performance, weather, species composition, and growth. ORNL/CDIAC-134, NDP-078A. Carbon Dioxide Information Analysis Center, US Department of Energy, Oak Ridge National Laboratory, Oak Ridge, Tennessee.
Harris WF, Goldstein RA, Henderson GS (1973) Analysis of forest biomass pools, annual primary production and turnover of biomass for a mixed deciduous forest watershed. In Young HE (Ed) Proceedings IUFRO Symposium Working Party on Forest Biomass. University of Maine Press, Orono, Maine, pp 43–64.
Hiers JK, Evans JP (1997) Effects of anthracnose on dogwood mortality and forest composition of the Cumberland Plateau (USA). Conser Biol 6:1430–1435.
Hinckley TM, Dougherty PM, Lassoie JP, Roberts JE, Teskey RO (1979) A severe drought: Impact on tree growth, phenology, net photosynthetic rate and water relations. Am Midi Nat 102:307–316.
Hinckley TM, Teskey RO, Duhme F, Richter H (1981) Temperate Hardwood Forests. In Kozlowski TT (Ed) Water deficits and plant growth, Vol VI. Academic Press, New York, pp 153–208.
Hoerl AE Jr. (1954) Fitting curves to data. In Perry JH (Ed) Chemical business handbook, McGraw-Hill, New York, pp 20–55 through 20–77.
Hursh CR, Haasis FW (1931) Effects of 1925 summer drought on southern appalachian hardwoods. Ecology 12: 380–386.
Jenkins MA, Pallardy SG (1995) The influence of drought on red oak group species growth and mortality in the Missouri Ozarks. Can J For Res 25:1119–1127.
Joslin JD, Wolfe MH (1998) Impacts of water input manipulations on fine root production and mortality in a mature hardwood forest. Plant Soil 204:165–174.
Keeland BD, Sharitz RR (1993) Accuracy of tree growth measurements using dendrometer bands. Can J For Res 23:2454–2457.
Kohyama T, Hara T (1989) Frequency distribution of tree growth rate in natural forest stands. Ann Bot 64:47–57.
Kramer PJ, Kozlowski TT (1979) Physiology of woody plants. Academic Press, New York.
Kozlowski TT (1982) Water supply and tree growth: Part 1 Water deficits. For Abst 43:57–95.
Kozlowski TT (1971) Measurement of cambial growth. In Kozlowski TT (Ed) Growth and development of trees. Academic Press, New York, pp 168–195.
Kuhns MR, Garrett HE, Teskey RO, Hinckley TM (1985) Root growth of black walnut trees related to soil temperature, soil water potential, and leaf water potential. For Sci 31:617–629.
McLaughlin SB, Downing DJ (1996) Interactive effects of ambient ozone and climate measured on growth of mature loblolly pine trees. Can J For Res 26:670–681.
McNulty SG, Swank WT (1995) Wood δ13C as a measure of annual basal area growth and soil water stress in a Pinus strobus forest. Ecology 76:1581–1586.
Orwig DA, Abrams MD (1997) Variation in radial growth responses to drought among species, site, and canopy strata. Trees 11:474–484.
Pedersen BS (1998) The role of stress in the mortality of midwestern oaks as indicated by growth prior to death. Ecology 79:79–93.
Pedersen BS (1999) The mortality of midwestern overstory oaks as a bioindicator of environmental stress. Ecol Appl 9:1017–1027.
Penninckx V, Meerts P, Herbauts J, Gruber W (1999) Ring width and element concentrations in beech (Fagus sylvatica L.) from a periurban forest in central Belgium. For Ecol Manage 113:23–33.
Phipps RL (1961) Analysis of five years dendrometer data obtained within three deciduous forest communities of Neotoma. Research Circular No. 105. Ohio Agricultural Experiment Station, Wooster, Ohio.
Robbins WJ (1921) Precipitation and the growth of oaks at Columbia, Missouri. Agriculture Experiment Station Research Bulletin 44. University of Missouri, College of Agriculture, Columbia, Missouri.
Small JA (1961) Drought response in William L. Hutcheson Memorial Forest, 1957. Bull Torrey Bot Club 88:180–183.
Sprugel DG, Benecke U (1991) Measuring woody-tissue respiration and photosynthesis. In Lassoie JP, Hinckley TM (Eds) Techniques and approaches in forest tree ecophysiology. CRC Press, Boca Raton, Florida, pp 329–355.
Swaine MD, Lieberman D, Putz FE (1987) The dynamics of tree populations in tropical forest—A review. J Trop Ecol 3:359–366.
Tainter FH, Fraedrich SW, Benson DM (1984) The effect of climate on growth, decline, and death of northern red oaks in the western North Carolina Nantahala Mountains. Castanea 49:127–137.
Teskey RO, Hinckley TM (1981) Influence of temperature and water potential on root growth of white oak. Physiol Plant 52:363–369.
Tschaplinski TJ, Gebre GM, Shirshac TL (1998) Osmotic potential of several hardwood species as affected by manipulation of throughfall precipitation in an upland oak forest during a dry year. Tree physiol 18:291–298.
Tuskan G, West D, Bradshaw HD, Neale D, Sewell M, Wheeler N, Megraw B, Jech K, Wiselogel A, Evans R, Elam C, Davis M, Dinus R (1999) Two high-throughput techniques for determining wood properties as part of a molecular genetics analysis of hybrid poplar and loblolly pine. Appl Biochem Biotech 77–79:55–65.
Vose JM, Swank WT (1994) Effects of long-term drought on the hydrology and growth of a white pine plantation in the southern Appalachians. For Ecol Manage 64:25–39.
Waring RH, Pitman GB (1985) Modifying lodgepole pine stands to change susceptibility to mountain pine beetle attack. Ecology 66:889–897.
Wilson KB, Baldocchi DD, Hanson PJ (2000a) Quantifying stomatal and non-stomatal limitations to carbon assimilation resulting from leaf aging and drought in mature deciduous tree species. Tree Physiol 20:787–797.
Wilson KB, Baldocchi DD, Hanson PJ (2000b) Spatial and seasonal variability of photosynthetic parameters and their relationship to leaf nitrogen in a deciduous forest. Tree Physiol 20:565–578.
Wilson KB, Baldocchi DD, Hanson PJ (2001) Leaf age affects the seasonal pattern of photosynthetic capacity and net ecosystem exchange of carbon in a deciduous forest. Plant Cell Environ 24:571–583.
Winget CH, Kozlowski TT (1964) Winter shrinkage of forest trees. J For 62:335–337.
Winget CH, Kozlowski TT (1965) Seasonal basal growth area as an expression of competition in northern hardwoods. Ecology 46:786–793.
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 2003 Springer Science+Business Media New York
About this chapter
Cite this chapter
Hanson, P.J., Todd, D.E., West, D.C., Edwards, N.T., Tharp, M.L., Simpson, W.A. (2003). Tree and Sapling Growth and Mortality. In: Hanson, P.J., Wullschleger, S.D. (eds) North American Temperate Deciduous Forest Responses to Changing Precipitation Regimes. Ecological Studies, vol 166. Springer, New York, NY. https://doi.org/10.1007/978-1-4613-0021-2_15
Download citation
DOI: https://doi.org/10.1007/978-1-4613-0021-2_15
Publisher Name: Springer, New York, NY
Print ISBN: 978-1-4612-6506-1
Online ISBN: 978-1-4613-0021-2
eBook Packages: Springer Book Archive