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Chapter 3 - The trunk and branches: more than a connecting drainpipe

Published online by Cambridge University Press:  05 July 2014

Peter A. Thomas
Affiliation:
Keele University
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Summary

The woody skeleton

What makes a tree different from other plants is the trunk (or bole) and branches making up the woody skeleton. The main job of this tough, long-lasting skeleton is to display the leaves up high above other lesser plants in the battle for light. As well as support, though, the trunk and branches have two other important jobs: getting water from the roots to the leaves and moving food around the tree to keep all parts, including the roots, alive. But is the trunk just a large connecting drainpipe that keeps the two ends of the trees apart? In many senses ‘yes’ but its structure allows it to do many other things that no mere drainpipe could do.

Starting from the outside is the outer bark, a waterproof layer, over the inner bark or phloem (Figure 3.1). The phloem is made up of living tissue that transports the sugary sap from the leaves to the rest of the tree. Inside the bark is the cambium which, as will be shown, is responsible for the tree getting fatter. Inside this again is the wood proper or xylem. Although seemingly ‘solid wood’ it is the part of the tree responsible for carrying water from the roots to the rest of the tree. The water moves upwards through dead empty cells. But wood is not entirely dead. Running from the centre of the tree are rays of living tissue (made up of thin-walled ‘parenchyma’ cells) which reach out into the bark (and in some trees there are lines of these living cells running up through the wood as well). As will be seen later these living cells are involved with movement and storage of food and the creation of heartwood, the dense central core of wood that (reputedly) supports the tree as it becomes larger. At the very centre of the tree, some trees, but not all, have a core of pith (the strengthening tissue when the shoot was very young and soft).

Type
Chapter
Information
Trees
Their Natural History
, pp. 51 - 101
Publisher: Cambridge University Press
Print publication year: 2014

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References

Aloni, R., Alexander, J.D. & Tyree, M.T. (1997) Natural and experimentally altered hydraulic architecture of branch junctions in Acer saccharum Marsh. and Quercus velutina Lam. trees. Trees, 11, 255–264.Google Scholar
Ambrose, A.R., Sillett, S.C. & Dawson, T.E. (2009) Effects of tree height on branch hydraulics, leaf structure and gas exchange in California redwoods. Plant, Cell and Environment, 32, 743–757.CrossRefGoogle ScholarPubMed
Angeles, G., Bond, B., Boyer, J.S., et al. (2004) The Cohesion-Tension Theory. New Phytologist, 163, 451–452.Google Scholar
Čermák, J., Kučera, J., Bauerle, W.L., Phillips, N. & Hinckley, T.M. (2007) Tree water storage and its diurnal dynamics related to sap flow and changes in stem volume in old-growth Douglas-fir trees. Tree Physiology, 27, 181–198.CrossRefGoogle ScholarPubMed
Cirelli, D., Jagels, R. & Tyree, M.T. (2004) Toward an improved model of maple sap exudation: the location and role of osmotic barriers in sugar maple, butternut and white birch. Tree Physiology, 28, 1145–1155.CrossRefGoogle Scholar
Cochard, H. (1992) Vulnerability of several conifers to air embolism. Tree Physiology, 11, 73–83.CrossRefGoogle ScholarPubMed
Cohen, Y., Cohen, S., Cantuarias-Aviles, T. & Schiller, G. (2008) Variations in the radial gradient of sap velocity in trunks of forest and fruit trees. Plant and Soil, 305, 49–59.CrossRefGoogle Scholar
Cramer, M.D. (2012) Unravelling the limits to tree height: a major role for water and nutrient trade-offs. Oecologia, 169, 61–72.CrossRefGoogle Scholar
Delzon, S., Douthe, C., Sala, A. & Cochard, H. (2010) Mechanisms of water-stress induced cavitation in conifers: bordered pit structure and function support the hypothesis of seal capillary-seeding. Plant, Cell & Environment, 33, 2101–2111.CrossRefGoogle Scholar
Domec, J.-C., Lachenbruch, B., Meinzer, F.C., Woodruff, D.R., Warren, J.M. & McCulloh, K.A. (2008) Maximum height in a conifer is associated with conflicting requirements for xylem design. Proceedings of the National Academy of Sciences, 105, 12069–12074.CrossRefGoogle Scholar
Du, S. & Yamamoto, F. (2007) An overview of the biology of reaction wood formation. Journal of Integrative Plant Biology, 49, 131–143.CrossRefGoogle Scholar
Hacke, U. & Sauter, J.J. (1996) Xylem dysfunction during winter and recovery of hydraulic conductivity in diffuse-porous and ring-porous trees. Oecologia, 105, 435–439.CrossRefGoogle Scholar
Hacke, U.G. & Sperry, J.S. (2001) Functional and ecological xylem anatomy. Perspectives in Plant Ecology, Evolution and Systematics, 4, 97–115.CrossRefGoogle Scholar
Jensen, K.H., Liesche, J., Bohr, T. & Schulz, A. (2012) Universality of phloem transport in seed plants. Plant, Cell & Environment, 35, 1065–1076.CrossRefGoogle ScholarPubMed
Koch, G.W., Sillett, S.C., Jennngs, G.M. & Davis, S.D. (2004) The limits to tree height. Nature, 428, 851–854.CrossRefGoogle ScholarPubMed
Milburn, J.A. (1996) Sap ascent in vascular plants: challengers to the cohesion theory ignore the significance of immature xylem and the recycling of Münch water. Annals of Botany, 78, 399–407.CrossRefGoogle Scholar
Milburn, J.A. & Zimmermann, M.H. (1986) Sapflow in the sugar maple in the leafless state. Journal of Plant Physiology, 124, 331–344.CrossRefGoogle Scholar
North, G.B. (2004) A long drink of water: how xylem changes with depth. New Phytologist, 163, 447–449.CrossRefGoogle Scholar
Novaes, E., Kirst, M., Chiang, V., Winter-Sederoff, H. & Sederoff, R. (2010) Lignin and biomass: a negative correlation for wood formation and lignin content in trees. Plant Physiology, 154, 555–561.CrossRefGoogle ScholarPubMed
Offenthaler, I., Hietz, P. & Richter, H. (2001) Wood diameter indicates diurnal and long-term patterns of xylem water potential in Norway spruce. Trees, 15, 215–221.CrossRefGoogle Scholar
Ohashi, S., Okada, N., Nobuchi, T., Siripatanadilok, S. & Veenin, T. (2009) Detecting invisible growth rings of trees in seasonally dry forests in Thailand: isotopic and wood anatomical approaches. Trees, 23, 813–822.CrossRefGoogle Scholar
Oldham, A.R., Sillett, S.C., Tomescu, A.M.F. & Koch, G.W. (2010) The hydrostatic gradient, not light availability, drives height-related variation in Sequoia sempervirens (Cupressaceae) leaf anatomy. American Journal of Botany, 97, 1087–1097.CrossRefGoogle Scholar
Panshin, A.J. & de Zeeuw, C. (1980) Textbook of Wood Technology (4th edn). McGraw-Hill, New York.Google Scholar
Putz, F.E., Coley, P.D., Lu, K., Montalvo, A. & Aiello, A. (1983) Uprooting and snapping of trees – structural determinants and ecological consequences. Canadian Journal of Forest Research, 13, 1011–1020.CrossRefGoogle Scholar
Read, H.J. (1996) Pollard and Veteran Tree Management II. Richmond Publishing, London.Google Scholar
Rose, D.R. (1987) Lightning damage to trees in Britain. Arboriculture Research Note 68/87/PAT.
Russo, S.E., Jenkins, K.L., Wiser, S.K., Uriarte, M., Duncan, R.P. & Coomes, D.A. (2010) Interspecific relationships among growth, mortality and xylem traits of woody species from New Zealand. Functional Ecology, 24, 253–262.CrossRefGoogle Scholar
Sano, Y. & Fukazawa, Y. (1996) Timing of the occurrence of frost cracks in winter. Trees, 11, 47–53.CrossRefGoogle Scholar
Slater, D. & Harbinson, C. (2010) Towards a new model of branch attachment. Arboricultural Journal, 33, 95–105.CrossRefGoogle Scholar
Soliz-Gamboa, C.C., Rozendaal, D.M.A., Ceccantini, G., et al. (2011) Evaluating the annual nature of juvenile rings in Bolivian tropical rainforest trees. Trees, 25, 17–27.CrossRefGoogle Scholar
Sorz, J. & Hietz, P. (2006) Gas diffusion through wood: implications for oxygen supply. Trees, 20, 34–41.CrossRefGoogle Scholar
Sperry, J.S., Meinzer, F.C. & McCulloh, K.A. (2008) Safety and efficiency conflicts in hydraulic architecture: scaling from tissues to trees. Plant, Cell and Environment, 31, 632–645.CrossRefGoogle ScholarPubMed
Tognetti, R. & Borghetti, M. (1994) Formation and seasonal occurrence of xylem embolism in Alnus cordata. Tree Physiology, 14, 241–250.CrossRefGoogle ScholarPubMed
Tyree, M.T. & Sperry, J.S. (1988) Do woody plants operate near the point of catastrophic xylem dysfunction caused by dynamic water stress? Answers from a model. Plant Physiology, 88, 574–580.CrossRefGoogle ScholarPubMed
Wheeler, T.D. & Stroock, A.D. (2008) The transpiration of water at negative pressures in a synthetic tree. Nature, 455, 208–212.CrossRefGoogle Scholar
Zimmermann, M.H. (1983) Xylem Structure and the Ascent of Sap. Springer, Berlin.CrossRefGoogle Scholar
Zimmermann, U., Schneider, H., Wegner, L.H. & Haase, A. (2004) Water ascent in tall trees: does evolution of land plants rely on a highly metastable state?New Phytologist 162, 575–615.CrossRefGoogle Scholar

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