TY - JOUR
T1 - Needle cell elongation and maturation timing derived from pine needle cellulose δ18O
AU - Wright, William E.
AU - Leavitt, Steven W.
PY - 2006/1
Y1 - 2006/1
N2 - Estimates of the timing of Pinus arizonica Engelm. needle development in 1998 and 1999 were derived from the leaf-cellulose δ18O of weekly growth increments. Significant correlations were noted between time series of local humidity and leaf-cellulose δ18O for needles growing near Tucson, Arizona. Correlations with temperature were also significant, but much lower, suggesting these variations in cellulose δ18O were determined mostly by changes in humidity. The timing of all significant correlations lags the timing of the appearance of the new needle growth, and is interpreted as indicating 16-23 d were required for cell enlargement in 1998 and 13-17 d in 1999. Similarly, properties of the environmental time series, when significantly correlated, are interpreted as indicating the duration of cellulose deposition (7-27 d in 1998, 13-21 d in 1999). Variations in stable-isotope back diffusion (the Péclet effect) and the synthesis of cellulose using stored photosynthate are discussed as explanations for departures from a Craig and Gordon-type model of leaf water δ18O. The Péclet effect, use of stored photosynthate, and variations in the growing-season source-water δ18O, probably confound the development of a high-resolution paleohumidity proxy from subfossil needle cellulose δ18O in this region.
AB - Estimates of the timing of Pinus arizonica Engelm. needle development in 1998 and 1999 were derived from the leaf-cellulose δ18O of weekly growth increments. Significant correlations were noted between time series of local humidity and leaf-cellulose δ18O for needles growing near Tucson, Arizona. Correlations with temperature were also significant, but much lower, suggesting these variations in cellulose δ18O were determined mostly by changes in humidity. The timing of all significant correlations lags the timing of the appearance of the new needle growth, and is interpreted as indicating 16-23 d were required for cell enlargement in 1998 and 13-17 d in 1999. Similarly, properties of the environmental time series, when significantly correlated, are interpreted as indicating the duration of cellulose deposition (7-27 d in 1998, 13-21 d in 1999). Variations in stable-isotope back diffusion (the Péclet effect) and the synthesis of cellulose using stored photosynthate are discussed as explanations for departures from a Craig and Gordon-type model of leaf water δ18O. The Péclet effect, use of stored photosynthate, and variations in the growing-season source-water δ18O, probably confound the development of a high-resolution paleohumidity proxy from subfossil needle cellulose δ18O in this region.
KW - Cell enlargement
KW - Cell wall maturation
KW - Humidity
KW - Needle elongation
KW - Oxygen isotope ratio
KW - Péclet effect
KW - Secondary cell wall
KW - δO
UR - http://www.scopus.com/inward/record.url?scp=33645081459&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=33645081459&partnerID=8YFLogxK
U2 - 10.1111/j.1365-3040.2005.01394.x
DO - 10.1111/j.1365-3040.2005.01394.x
M3 - Article
C2 - 17086748
AN - SCOPUS:33645081459
SN - 0140-7791
VL - 29
SP - 1
EP - 14
JO - Plant, Cell and Environment
JF - Plant, Cell and Environment
IS - 1
ER -