Investigating the effect of neighbour competition on individual tree growth in thinned and unthinned eucalypt forests

2021 ◽  
Vol 499 ◽  
pp. 119637
Author(s):  
Shes Kanta Bhandari ◽  
Erik J. Veneklaas ◽  
Lachlan McCaw ◽  
Richard Mazanec ◽  
Michael Renton
2019 ◽  
Vol 65 (6) ◽  
pp. 784-795
Author(s):  
Jeffrey S Ward ◽  
Jessica Wikle

AbstractSix study areas were established in 80–125-year-old upland oak stands on average sites to compare stand and individual tree growth response following two active treatments (B-level thinning, crop tree) with an unmanaged control. Initial stocking of 104 percent was reduced to 62 percent and 60 percent on the B-level and crop-tree-management plots, respectively. Approximately 7,200 board feet per acre (International ¼) were harvested on the actively managed plots with upland oaks accounting for 81 percent of pre- and 86 percent of residual stand. Eleven-year diameter and volume growth of oak sawtimber trees was greater on actively managed plots. Growth response increased with degree of release and was maintained for the length of the study. Because of the increased individual tree growth of oaks in response to release, stand volume growth of oak sawtimber did not differ between treatments. In contrast to an 11-year decline of poletimber stocking on unmanaged plots, poletimber stocking increased on managed plots as diameter growth increased in response to partial release. This may increase difficulty of regenerating oak in the future. For those mature red oak stands where traditional regeneration prescriptions will not be implemented or will be delayed, commercial harvests can be conducted without compromising stand volume growth of oak.


1995 ◽  
Vol 25 (1) ◽  
pp. 69-80 ◽  
Author(s):  
P.W. West ◽  
G.H.R. Osier

The factors determining individual tree growth response are examined during the 4 years following thinning in experiments in even-aged, 8- or 12-year-old regrowth Eucalyptusregnans F. Muell. forest at two sites in southern Australia. At one site, a vigorous understorey dominated by a sedge developed after the thinning. At that site, light-use efficiency by the trees was unaffected by thinning and the aboveground biomass production by the trees in the thinned stand was substantially less than that in the unthinned stand. At the other site, little understorey developed, light-use efficiency by trees in the thinned stand was greater than that in the unthinned stand, and aboveground biomass production was unaffected by thinning even though the leaf weight of the thinned stand was far below that of the unthinned stand. Where the understorey developed, it was concluded that it competed successfully with the trees for water, thereby reducing production in the thinned stand when compared with the unthinned stand. The individual tree growth response that occurred in the thinned stand at that site appeared to be due soley to the extra light available to individual trees following the canopy opening. Where the understorey did not develop, it was concluded that individual tree growth response was due not only to the extra light available to individual trees but also to the increased availability of belowground resources, most probably soil water. Application of a pre-existing stand growth model suggested that at that site the tendency for increased growth resulting from extra water availability in the thinned stand was just balanced by decreased growth due to lower radiation absorption by the reduced canopy, so that net production was unaffected by thinning.


2001 ◽  
Vol 154 (1-2) ◽  
pp. 261-276 ◽  
Author(s):  
Julian C. Fox ◽  
Peter K. Ades ◽  
Huiquan Bi

1992 ◽  
Vol 22 (5) ◽  
pp. 660-666 ◽  
Author(s):  
Paul C. Van Deusen

A number of recent studies have shown reduced stand-level and individual-tree growth in natural loblolly pine (Pinustaeda L.) stands in the southeastern United States. This study uses increment cores from dominant and codominant trees to determine if individual-tree growth has changed from 1915 to 1985. The cores are grouped for comparison by first sorting on the basis of median stand age and then further sorting these groups of cores by individual-tree age. These trees experienced increasing basal area increments from the mid-1940s into the mid-1970s, after which growth rates returned to preincrease levels. These data support recent findings of growth reductions, but also indicate previously unreported growth increases preceding the growth decreases. These and supplemental permanent plot data suggest that stand dynamics is a viable hypothesis for explaining these growth trends.


2007 ◽  
Vol 126 (3) ◽  
pp. 473-473
Author(s):  
J. Schröder ◽  
H. Röhle ◽  
D. Gerold ◽  
K. Münder

1992 ◽  
Vol 22 (6) ◽  
pp. 905-914 ◽  
Author(s):  
David C. LeBlanc ◽  
N.S. Nicholas ◽  
S.M. Zedaker

The prevalence of individual-tree growth decline was determined for red spruce (Picearubens Sarg.) populations at three locations in the southern Appalachians: Mount Rogers National Recreation Area, the Black Mountains, and Great Smoky Mountain National Park. An index of annual stemwood volume increment (AVI) was computed from dendrochronological data and a site-specific DBH–height regression equation. Individual-tree AVI time series were analyzed to identify changes in 20-year periodic mean AVI and AVI trend. The proportion of red spruce that exhibited decreasing mean AVI or negative AVI trend was determined for the most recent 20-year period, and this was compared with the estimated historical prevalence of these indications of growth decline. Also, the prevalence of growth decline was compared among subpopulations that differed with regard to various tree, stand, and site characteristics. Of 263 red spruce sampled, 25% exhibited a decrease in mean AVI during the period 1967–1986, 8% exhibited a negative AVI trend without a reduction in mean AVI, and 17% exhibited a reduction in the slope of the AVI curve. The proportion of trees that exhibited decreasing or slowed growth after 1967 was substantially greater among trees growing at 1980 m than in populations at lower elevations; no relationship was found between elevation and growth decline below 1980 m. No difference was found in prevalence of growth decline between subpopulations that differed with regard to age, DBH, competitive status, stand density, slope aspect, or site exposure. The prevalence of individual-tree growth decline for the most recent 20-year period did not exceed estimated levels for historical periods of decline in the Great Smoky Mountains population.


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