Effect of local stand structure on leaf area, growth, and growth efficiency following thinning of white spruce

2016 ◽  
Vol 368 ◽  
pp. 55-62 ◽  
Author(s):  
Kwadwo Omari ◽  
David A. MacLean ◽  
Michael B. Lavigne ◽  
John A. Kershaw ◽  
Greg W. Adams
2014 ◽  
Vol 63 (1) ◽  
pp. 5-7 ◽  
Author(s):  
Andrzej Grzegorczyk

The leaf area growth in maize was approximated basing on the Richards function in the form of: y=A[l+b exp(-kt)]<sup>1/(1-m)</sup> . The constant coefficients of the Richards function were found by means of the Marquardt's method. The initial values of parameters were given basing on results of the preliminary approximation of the growth process by means of logistic function y = A[l+b exp(-kt)]<sup>-1</sup>. The procedure of nonlinear regression was found to be useful (curvilinear determination coefficient R<sup>2</sup> = 0.995). The Richards curve precisely describes the course of changes of the leaf area in maize since sprouting to a tassel flowering phase.


1995 ◽  
Vol 129 (2) ◽  
pp. 253-263 ◽  
Author(s):  
PETER S. CURTIS ◽  
CHRISTOPH S. VOGEL ◽  
KURT S. PREGITZER ◽  
DONALD R. ZAK ◽  
JAMES A. TEERI

1987 ◽  
Vol 17 (8) ◽  
pp. 951-956 ◽  
Author(s):  
C. P. Andersen ◽  
E. I. Sucoff ◽  
R. K. Dixon

Green ash (Fraxinuspennsylvanica Marsh.) seedlings were either inoculated with Glomusetunicatum or not inoculated and grown for approximately 5 weeks under glasshouse conditions to permit root colonization with vesicular–arbuscular (V–A) mycorrhizae. Two experiments were conducted to characterize V–A mycorrhizae influence on seedling growth at low root temperature. In experiment 1, seedlings were subjected to four root zone temperatures ranging from 7.5 to 20 °C for 24 days to measure leaf area and plant height on intact seedlings. In experiment 2, seedlings were exposed to root temperatures of 12.0, 16.0, and 20.0 °C for 30 days and seedlings were destructively harvested at 6-day intervals to measure growth variables and biomass distribution. Results of experiments 1 and 2 were similar. In experiment 1, leaf area growth of mycorrhizal seedlings was significantly greater than nonmycorrhizal controls at all temperatures. Relative leaf area growth rate was greater in mycorrhizal than nonmycorrhizal seedlings at 7.5 and 11.5 °C, similar between treatments at 15.5 °C, and greater in nonmycorrhizal seedlings at 20.0 °C, differences possibly resulting from the larger size of mycorrhizal seedlings at the start of the temperature treatments. In experiment 2, temperature treatments were imposed on seedlings of the same size. Mycorrhizal seedlings had greater leaf area growth rates and relative leaf area growth rates than nonmycorrhizal seedlings at all temperatures. Phosphorus concentrations and total P content in roots and leaves did not differ significantly between mycorrhizal treatments at any temperature; however, mycorrhizal seedlings had consistently greater leaf P content than nonmycorrhizal controls. Glomusetunicatum actively stimulates green ash growth at moderately low root temperatures.


1986 ◽  
Vol 66 (3) ◽  
pp. 677-682 ◽  
Author(s):  
W. S. FARGO ◽  
E. L. BONJOUR ◽  
T. L. WAGNER

An equation was developed which may be used to estimate the area of all sizes of developing squash (Cucurbita pepo L.) leaves. The equation uses two leaf measurements (midrib length (ML) and the distance between tertiary lobes (TD)) which may be taken quickly in the laboratory or field without disturbing the host plant. The equation is:[Formula: see text]The equation is applicable in monitoring individual leaf expansion as well as total plant leaf area increase and in examining the dynamics of the plant under various environmental conditions.Key words: Cucurbita pepo L., leaf area, growth, development, leaf expansion


2015 ◽  
Vol 6 ◽  
Author(s):  
Sarathi M. Weraduwage ◽  
Jin Chen ◽  
Fransisca C. Anozie ◽  
Alejandro Morales ◽  
Sean E. Weise ◽  
...  

1994 ◽  
Vol 24 (11) ◽  
pp. 2208-2221 ◽  
Author(s):  
Marie R. Coyea ◽  
Hank A. Margolis

The growth efficiencies (E; stemwood growth per unit leaf area) of balsam fir (Abiesbalsamea (L.) Mill.) trees from 20 stands were reconstructed over the 30-year period from 1960 to 1989 in order to determine if E could be used to predict tree mortality occurring during and after an epidemic of eastern spruce budworm (Choristoneurafumiferana (Clem.)). Growth efficiencies were reconstructed based on the relationship between age and the number of annual growth rings in the cross-sectional area of heartwood at breast height (R2 = 0.97) and on the previously demonstrated relationship between sapwood area and leaf area of balsam fir across a wide geographic area. Profile and logistic regression analyses demonstrated that apparent E (i.e., the historically reconstructed E) of surviving trees was greater than that of dead trees for every year of the 30-year analysis period. For trees in the 25- to 35-year age-class in 1960, apparent E was the only variable measured prior to the epidemic that was significantly related to balsam fir mortality. For all trees (aged 11 to 46 years in 1960), both tree age and apparent E were significant factors prior to the epidemic. During and following the epidemic, several of the more standard mensurational variables (e.g., diameter and basal area growth) were also significantly associated with balsam fir mortality, but apparent E had the highest levels of significance. Using logistical regression, critical E values below which trees would be predicted to die were calculated as 5-year running averages for the period prior to the epidemic (1960–1968). These were stable at around 0.17 × 10−4 m2 basal area growth•(m2 leaf area)−1•year−1. Following the epidemic, critical E values were again stable but at a lower level of around 0.07. There was a negative exponential relationship between apparent E and leaf area. Furthermore, for the same level of leaf area, surviving trees had a higher apparent E than trees that died, up to approximately 30 m2 of leaf area. These results suggest that growth efficiency should be considered as part of standard forest inventories in the balsam fir zone because of its ease of measure and its apparent ability to provide a sensitive, physiologically based index of forest health. Furthermore, the technique of historically reconstructing E demonstrated in this study may be of interest for other types of dendrochronological research.


2001 ◽  
Vol 4 (3) ◽  
pp. 184-188 ◽  
Author(s):  
Ma.Rebecca Laza ◽  
Shaobing Peng ◽  
Sanico Arnel ◽  
Visperas Romeo ◽  
Shigemi Akita

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