Refined pipe theory for mechanistic modeling of wood development

被引:29
作者
Deckmyn, Gaby [1 ]
Evans, Sam P.
Randle, Tim J.
机构
[1] Univ Antwerp, Res Grp Plant & Vegetat Ecol, B-2020 Antwerp, Belgium
[2] Alice Holt Lodge, Mensurat, Forest Res, Farnham, Surrey, England
关键词
simulation; tree growth; vessel radius; wood anatomy; wood density;
D O I
10.1093/treephys/26.6.703
中图分类号
S7 [林业];
学科分类号
0829 ; 0907 ;
摘要
We present a mechanistic model of wood tissue development in response to changes in competition, management and climate. The model is based on a refinement of the pipe theory, where the constant ratio between sapwood and leaf area (pipe theory) is replaced by a ratio between pipe conductivity and leaf area. Simulated pipe conductivity changes with age, stand density and climate in response to changes in allocation or pipe radius, or both. The central equation of the model, which calculates the ratio of carbon (C) allocated to leaves and pipes, can be parameterized to describe the contrasting stem conductivity behavior of different tree species: front constant stem conductivity (functional homeostasis hypothesis) to height-related reduction in stem conductivity with age (hydraulic limitation hypothesis). The model simulates the daily growth of pipes (vessels or tracheids), fibers and parenchyma as well as vessel size and simulates the wood density profile and the earlywood to late-wood ratio from these data. Initial runs indicate the model yields realistic seasonal changes in pipe radius (decreasing pipe radius from spring to autumn) and wood density, as well as realistic differences associated with the competitive status of trees (denser wood in Suppressed trees).
引用
收藏
页码:703 / 717
页数:15
相关论文
共 115 条
[71]  
MITCHELL KJ, 1989, CAN PULP PAP ASS WOO
[72]   Interaction between sapwood and foliage area in alpine ash (Eucalyptus delegatensis) trees of different heights [J].
Mokany, K ;
McMurtrie, RE ;
Atwell, BJ ;
Keith, H .
TREE PHYSIOLOGY, 2003, 23 (14) :949-957
[73]   Foliage biomass sapwood (area and volume) relationships of Tectona grandis LF and Gmelina arborea Roxb.:: silvicultural implications [J].
Morataya, R ;
Galloway, G ;
Berninger, F ;
Kanninen, M .
FOREST ECOLOGY AND MANAGEMENT, 1999, 113 (2-3) :231-239
[74]   Limitation of stomatal conductance by hydraulic traits: sensing or preventing xylem cavitation? [J].
Nardini, A ;
Salleo, S .
TREES-STRUCTURE AND FUNCTION, 2000, 15 (01) :14-24
[75]   Tree responses to rising CO2 in field experiments:: implications for the future forest [J].
Norby, RJ ;
Wullschleger, SD ;
Gunderson, CA ;
Johnson, DW ;
Ceulemans, R .
PLANT CELL AND ENVIRONMENT, 1999, 22 (06) :683-714
[76]   Nitrogen resorption in senescing tree leaves in a warmer, CO2-enriched atmosephere [J].
Norby, RJ ;
Long, TM ;
Hartz-Rubin, JS ;
O'Neill, EG .
PLANT AND SOIL, 2000, 224 (01) :15-29
[77]   Canopy and hydraulic conductance in young, mature and old Douglas-fir trees [J].
Phillips, N ;
Bond, BJ ;
McDowell, NG ;
Ryan, MG .
TREE PHYSIOLOGY, 2002, 22 (2-3) :205-211
[78]  
Pilcher J.R., 1995, PROBLEMS STABLE ISOT, P157
[79]   PATTERNS OF CHANGE OF SATURATED SAPWOOD PERMEABILITY AND SAPWOOD CONDUCTANCE WITH STAND DEVELOPMENT [J].
POTHIER, D ;
MARGOLIS, HA ;
WARING, RH .
CANADIAN JOURNAL OF FOREST RESEARCH, 1989, 19 (04) :432-439
[80]   The single tree-based stand simulator SILVA: construction, application and evaluation [J].
Pretzsch, H ;
Biber, P ;
Dursky, J .
FOREST ECOLOGY AND MANAGEMENT, 2002, 162 (01) :3-21