Literature DB >> 16639568

Hydraulic compensation in northern Rocky Mountain conifers: does successional position and life history matter?

Anna Sala1.   

Abstract

As trees grow tall and the resistance of the hydraulic pathway increases, water supply to foliage may decrease forcing stomata to close and CO2 uptake to decline. Several structural (e.g. biomass allocation) and physiological adjustments, however, may partially or fully compensate for such hydraulic constraints and prevent limitations on CO2 uptake and growth. The degree to which trees compensate for hydraulic constraints as they grow tall may depend on the costs and benefits associated with hydraulic compensation according to their ecology and life history. Because later successional Rocky Mountain conifers are more shade tolerant, optimization of CO2 uptake as trees grow tall and shade increases may confer greater benefits than in earlier successional species. If so, higher compensation for hydraulic constraints is expected in later successional species relative to co-occurring earlier successional species. I have examined height-related changes of crown stomatal conductance on a leaf area basis (G(LA)) and leaf to sapwood ratios (A(L):A(S)) for five conifer species in the northern Rocky Mountains. Species were arranged in pairs, each pair consisting of an early and late successional species. For high elevations I used, respectively, whitebark pine (Pinus albicaulis) and subalpine fir (Abies lasiocarpa); for mid-elevations, western larch (Larix occidentalis) and Douglas-fir (Pseudotsuga menziesii); for lower elevations, ponderosa pine (Pinus ponderosa) and Douglas-fir. A(L):A(S) either decreased (subalpine fir, ponderosa pine), remained constant (Douglas-fir, western larch) or increased (whitebark pine) with tree height. As hypothesized, earlier successional species (ponderosa pine, whitebark pine and western larch) exhibited significantly stronger decreases of G(LA) with tree height relative to their later successional pairs (Douglas-fir and subalpine fir), which fully compensated for height-related hydraulic constraints on G(LA). A life history approach that takes into account the optimization of size- and species-specific ecological functions may also help researchers better understand biomass allocation and hydraulic function in trees.

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Year:  2006        PMID: 16639568     DOI: 10.1007/s00442-006-0420-5

Source DB:  PubMed          Journal:  Oecologia        ISSN: 0029-8549            Impact factor:   3.225


  21 in total

1.  Limitations of a compensation heat pulse velocity system at low sap flow: implications for measurements at night and in shaded trees.

Authors:  Peter Becker
Journal:  Tree Physiol       Date:  1998-03       Impact factor: 4.196

2.  Assessing variation in the radial profile of sap flux density in Pinus species and its effect on daily water use.

Authors:  Chelcy R Ford; Mary Anne McGuire; Robert J Mitchell; Robert O Teskey
Journal:  Tree Physiol       Date:  2004-03       Impact factor: 4.196

3.  THEORY OF MAST REPRODUCTION IN PLANTS: STORAGE-SIZE DEPENDENT STRATEGY.

Authors:  Atsushi Yamauchi
Journal:  Evolution       Date:  1996-10       Impact factor: 3.694

4.  Water use by whitebark pine and subalpine fir: potential consequences of fire exclusion in the northern Rocky Mountains.

Authors:  A Sala; E V Carey; R E Keane; R M Callaway
Journal:  Tree Physiol       Date:  2001-07       Impact factor: 4.196

5.  Dwarf mistletoe affects whole-tree water relations of Douglas fir and western larch primarily through changes in leaf to sapwood ratios.

Authors:  Anna Sala; Eileen V Carey; Ragan M Callaway
Journal:  Oecologia       Date:  2001-01-01       Impact factor: 3.225

6.  Age-related effects on leaf area/sapwood area relationships, canopy transpiration and carbon gain of Norway spruce stands (Picea abies) in the Fichtelgebirge, Germany.

Authors:  B Köstner; E Falge; J D Tenhunen
Journal:  Tree Physiol       Date:  2002-06       Impact factor: 4.196

7.  Adjustments in hydraulic architecture of Pinus palustris maintain similar stomatal conductance in xeric and mesic habitats.

Authors:  R N Addington; L A Donovan; R J Mitchell; J M Vose; S D Pecot; S B Jack; U G Hacke; J S Sperry; R Oren
Journal:  Plant Cell Environ       Date:  2006-04       Impact factor: 7.228

8.  The limits to tree height.

Authors:  George W Koch; Stephen C Sillett; Gregory M Jennings; Stephen D Davis
Journal:  Nature       Date:  2004-04-22       Impact factor: 49.962

9.  An investigation of hydraulic limitation and compensation in large, old Douglas-fir trees.

Authors:  Nate G McDowell; Nathan Phillips; Claire Lunch; Barbara J Bond; Michael G Ryan
Journal:  Tree Physiol       Date:  2002-08       Impact factor: 4.196

10.  Estimating water use by sugar maple trees: considerations when using heat-pulse methods in trees with deep functional sapwood.

Authors:  Roman C. Pausch; Edmund E. Grote; Todd E. Dawson
Journal:  Tree Physiol       Date:  2000-03       Impact factor: 4.196

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