Growth decline of wind-exposed red spruce and balsam fir in the White Mountains

1986 ◽  
Vol 16 (2) ◽  
pp. 232-238 ◽  
Author(s):  
T. C. Harrington

Overstory red spruce (Picearubens Sarg.) and balsam fir (Abiesbalsamea (L.) Mill.) trees suddenly exposed to strong, turbulent winds along a ski trail cut in 1962 in New Hampshire showed growth (increment of basal area) reductions during 1974 through 1983 of 82 and 63%, respectively, compared with growth during 1954 through 1963. Growth of comparable trees on the upwind side of the ski trail did not decline during this period. Mechanical damage to crowns and roots during tree sway is proposed as the primary cause of the growth decline. Six downwind fir trees had smaller living crowns, fewer living fine roots, more abrasion wounds on woody roots, and more discoloration of root wood than did the six fir trees on the upwind side of the trail. Six downwind spruce trees had smaller living crowns and more root discoloration than did the six upwind spruce trees. Regression analyses were made using the 24 trees along the ski trail and 29 trees from two other poorly stocked and declining stands in the White Mountains. Of the site, stand, and tree parameters tested, only root and crown damage parameters significantly correlated with reductions in growth rate. For fir, percent root discoloration and percent roots abraded explained 82% of the variation in growth decline. For spruce, crown loss explained 70% of the variation. The symptomatology of these wind-stressed trees was consistent with that described for spruce–fir decline. Although acid deposition or some other anthropogenic stress has been proposed as the primary cause of spruce–fir decline, wind appears to be an overlooked but significant natural stress factor that could explain at least some of the growth decline and mortality of spruce and fir at high elevations in the northern Appalachian Mountains.

1986 ◽  
pp. 1479-1484
Author(s):  
J. W. Hornbeck ◽  
R. B. Smith ◽  
C. A. Federer

2009 ◽  
Vol 26 (2) ◽  
pp. 68-75 ◽  
Author(s):  
Philip V. Hofmeyer ◽  
Robert S. Seymour ◽  
Laura S. Kenefic

Abstract Basal area growth of outwardly sound northern white-cedar (Thuja occidentalis L.) was compared with that of balsam fir (Abies balsamea [L.] Mill.) and red spruce (Picea rubens Sarg.) across site and light exposure class gradients on 60 sites throughout northern Maine. Once adjusted for sapwood area, northern white-cedar basal area growth was not strongly affected by site or light exposure class; growth was similar to that of red spruce but generally lower than that of balsam fir. Site index did not differ appreciably among soil drainage classes for red spruce and northern white-cedar, although small sample size limited analysis on upland site classes. Incidence of central decay was higher in northern white-cedar than balsam fir, which was higher than red spruce. Incidence of decay in outwardly sound northern white-cedar and balsam fir was highest on well-drained mineral soils, and mean proportion of basal area decayed at breast height increased in outwardly sound northern white-cedar as drainage improved from poorly drained to well-drained soils. These data suggest that northern white-cedar on lowland organic and poorly drained mineral soils in Maine have less decay, similar basal area growth, and similar site index relative to upland northern white-cedar communities.


2003 ◽  
Vol 20 (4) ◽  
pp. 148-153 ◽  
Author(s):  
Dale S. Solomon ◽  
Lianjun Zhang ◽  
Thomas B. Brann ◽  
David S. Larrick

Abstract Cumulative and annual mortality of red spruce (Picea rubens Sarg.) and balsam fir [Abies balsamea (L.) Mill.] were examined over a 10 yr period to follow the mortality patterns in unprotected spruce-fir forests in northern Maine. Different mortality patterns were determined based on stand composition classes and merchantability classes. In general, balsam fir was more vulnerable to budworm attack, and reached 92–100% basal area mortality and 84–97% stem density mortality 12 yr after the start of the outbreak. Red spruce, in contrast, had approximately 32–59% basal area mortality and 30–66% stem density mortality during the same time period. Balsam fir mortality started 1 to 2 yr before spruce, while spruce mortality continued 2 to 3 yr after fir mortality was completed. Higher mortality was found in smaller trees than sawtimber-sized trees. Stands with hardwood components (30–70% in basal area) had the lowest mortality rate for both species. Furthermore, Schnute growth function (Schnute 1981) was used to characterize the cumulative mortality trajectories after the defoliation of spruce and fir by stand composition classes. The models estimated the time when annual mortality achieved maximum, the cumulative mortality at that time, and the asymptotic mortality over a long time period after the start of the attack. The information can provide guidelines for predicting protection strategies and scheduling salvage harvests.


1986 ◽  
Vol 31 (1-2) ◽  
pp. 425-430 ◽  
Author(s):  
J. W. Hornbeck ◽  
R. B. Smith ◽  
C. A. Federer

1988 ◽  
Vol 18 (8) ◽  
pp. 991-1001 ◽  
Author(s):  
D. M. Rizzo ◽  
T. C. Harrington

Crown dieback and mortality of red spruce and balsam fir in the subalpine zone of the northern Appalachian Mountains have been attributed to wind-induced crown and root damage. Vertical root movements, damage to roots and crowns, and growth rate were measured on wind-exposed spruce and fir trees near canopy gaps at Kancamagus Pass (875 m elevation) and Wildcat Mountain (1160 m) in the White Mountain National Forest, New Hampshire. Root movements were significantly correlated with windspeed, crown exposure, and depth of soil to rock. Woody roots that had made movements in excess of 10 mm had fewer small (1–3 mm diameter) roots, more abrasion wounds, and a greater amount of nonconducting (dry or discolored) xylem than roots that had made smaller movements. Hydraulic conductivity was significantly reduced in roots with greater than 40% xylem cross-sectional area that was nonconducting. Spruce and fir trees at gap margins grew slower and had more root and crown damage than trees sheltered within the canopy. Decreases in growth rate of spruce and fir trees at both sites during the past 20 years were significantly correlated with wind exposure and some of the root and crown damage variables.


1985 ◽  
Vol 15 (6) ◽  
pp. 1199-1201 ◽  
Author(s):  
James W. Hornbeck ◽  
Robert B. Smith

Data from a study of 3001 dominant or codominant red spruces (Picearubens Sarg.) across New England and the Adirondacks showed that their annual growth in basal area increased consistently from 1910–1920 to about 1960. It then fluctuated around a generally declining trend and by the early 1980's was 13 to 40% below its peak. Defoliation by the spruce budworm, climate change, maturation of the forest, and acid deposition are all possible explanations.


1988 ◽  
Vol 18 (10) ◽  
pp. 1337-1340 ◽  
Author(s):  
J. W. Hornbeck ◽  
R. B. Smith ◽  
C. A. Federer

Tree-ring measurements on increment cores collected from more than 5000 trees during a periodic survey of forest resources in New England indicate trends in regional basal-area increment by species for the period 1950–1980. Two species, red spruce and balsam fir, have had generally decreasing growth rates since the 1960s. Normal aging of the low-elevation, even-aged spruce–fir forest is a probable cause. Eight other species, including sugar maple, had constant or increasing growth throughout the period. White pine had considerably higher growth rates than the other species.


1988 ◽  
Vol 18 (6) ◽  
pp. 723-727 ◽  
Author(s):  
Hank A. Margolis ◽  
Robert R. Gagnon ◽  
David Pothier ◽  
Marius Pineau

Balsam fir trees established from advanced regeneration following a clear-cut in 1970 were pruned in June 1985 to live crown ratios of 0.6, 0.4, and 0.2 compared with control trees, which had live crown ratios of 0.8. After two growing seasons, we investigated the homeostatic adjustment of these trees to the loss of their foliage. The height growth, basal area growth, sapwood cross-sectional area, heartwood area, and sapwood saturated permeability of the trees that were pruned to a 0.6 live crown ratio were not significantly different from those of the controls. On the other hand, height growth increment following pruning was reduced 16.7 cm (23%) and 19.5 cm (27%) for the trees pruned to 0.4 and 0.2 live crown ratios, respectively. Furthermore, basal area growth following pruning was reduced 3.2 cm2 (30%) and 6.5 cm2 (61%), respectively. While trees in both the 0.4 and 0.2 live crown ratio pruning treatments did adjust their breast height sapwood area in response to the removal of foliage, the nature of this adjustment differed between the two treatments. For the trees with the 0.4 live crown ratio, sapwood area was reduced because of a reduction in basal area growth but the area of heartwood remained unchanged. For the trees with the 0.2 live crown ratio, the changes in sapwood area were due both to a reduction in basal area growth and an expansion of the heartwood. The saturated permeability of sapwood was not significantly affected by pruning. The adaptive implications of balsam fir's response to the loss of foliage are discussed in terms of the optimizing the allocation of a limited amount of available carbon.


1982 ◽  
Vol 12 (3) ◽  
pp. 617-626 ◽  
Author(s):  
Jeffrey R. Foster ◽  
Gerald E. Lang

Decomposition rates for red spruce (Picearubens Sarg.) and balsam fir (Abiesbalsamea (L.) Mill.) boles on the forest floor were determined for midelevation forests of the White Mountains from a chronosequence of previously logged stands. Density changes in wood and bark were described using a negative exponential model, yielding decay constants of 0.033 and 0.029/year for spruce and fir wood, respectively. The two species were not statistically different in terms of mass loss. Bole diameter had no influence on the decay rate of red spruce. Fir boles in midelevation forests decayed significantly faster than those in high-elevation forests measured in another study. Net accumulation of N, P, Ca, and Mg occurred in the wood of both species. N accumulated in bark, but P, Ca, and Mg behavior was variable. Na and K behavior was similar in the wood and bark of both species, with Na release concomitant with mass loss, while K was lost faster than mass. C:N ratios declined, and N:P ratios converged on a value of ca. 20, in the wood and bark of both species.


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