scholarly journals In situ decomposition of northern hardwood tree boles: decay rates and nutrient dynamics in wood and bark

2014 ◽  
Vol 44 (12) ◽  
pp. 1515-1524 ◽  
Author(s):  
Chris E. Johnson ◽  
Thomas G. Siccama ◽  
Ellen G. Denny ◽  
Mary Margaret Koppers ◽  
Daniel J. Vogt
Keyword(s):  
Mass Loss ◽  
Sugar Maple ◽  
Nutrient Dynamics ◽  
Exponential Model ◽  
Fagus Grandifolia ◽  
Decay Rates ◽  
Nutrient Concentrations ◽  
Betula Alleghaniensis ◽  
Northern Hardwood ◽  
Clear Cutting

The decomposition of coarse woody debris contributes to forest nutrient sustainability and carbon (C) balances, yet few field studies have been undertaken to investigate these relationships in northern hardwood forests. We used a paired-sample approach to study the decomposition of sugar maple (Acer saccharum Marsh.), American beech (Fagus grandifolia Erhr.), and yellow birch (Betula alleghaniensis Britt.) boles at the Hubbard Brook Experimental Forest in New Hampshire. Mass loss over 16 years followed a first-order exponential decay pattern with half-lives ranging from 4.9 to 9.4 years in bark and from 7.3 to 10.9 years in wood. Nitrogen (N) and phosphorus (P) concentrations increased significantly during decomposition, resulting in sharp decreases in C:N and C:P ratios. We did not, however, observe significant net increases in the amount of N or P stored in decomposing boles, as reported in some other studies. Calcium (Ca) concentration decreased by up to 50% in bark but more than doubled in wood of all species. The retention of Ca in decomposing wood helps maintain Ca pools in this base-poor ecosystem. Together, the exponential model for mass loss and a combined power-exponential model for changes in nutrient concentrations were able to simulate nutrient dynamics in decomposing boles after clear-cutting in an adjacent watershed.

scholarly journals Height Development of Upper-Canopy Trees Within Even-Aged Adirondack Northern Hardwood Stands

2004 ◽  
Vol 21 (3) ◽  
pp. 117-122 ◽  
Author(s):  
Ralph D. Nyland ◽  
David G. Ray ◽  
Ruth D. Yanai
Keyword(s):  
Sugar Maple ◽  
Height Growth ◽  
Fagus Grandifolia ◽  
Growth Patterns ◽  
Betula Alleghaniensis ◽  
Yellow Birch ◽  
Northern Hardwood ◽  
White Ash ◽  
Advance Regeneration ◽  
Canopy Trees

Abstract Knowledge of the relative rates of height growth among species is necessary for predicting developmental patterns in even-aged northern hardwood stands. To quantify these relationships, we used stem analysis to reconstruct early height growth patterns of dominant and codominant sugar maple (Acer saccharum Marsh.), yellow birch (Betula alleghaniensis Britton), white ash (Fraxinus americana L.), and America beech (Fagus grandifolia Ehrh.) trees. We used three stands (aged 19, 24, and 29 years) established by shelterwood method cutting preceded by an understory herbicide treatment. We analyzed 10 trees of each species per stand. Height growth was similar across stands, allowing us to develop a single equation for each species. Our data show that yellow birch had the most rapid height growth up to approximately age 10. Both sugar maple and white ash grew more rapidly than yellow birch beyond that point. Beech consistently grew the slowest. White ash had a linear rate of height growth over the 29-year period, while the other species declined in their growth rates. By age 29, the heights of main canopy trees ranged from 38 ft for beech to 51 ft for white ash. Both yellow birch and sugar maple averaged 46 ft tall at that time. By age 29, the base of the live crown had reached 17, 20, 21, and 26 ft for beech, sugar maple, yellow birch, and white ash, respectively. Live–crown ratios of upper-canopy trees did not differ appreciably among species and remained at approximately 40% for the ages evaluated. These results suggest that eliminating advance regeneration changes the outcome of competition to favor species other than beech. North. J. Appl. For. 21(3):117–122.

Calcium and magnesium in wood of northern hardwood forest species: relations to site characteristics

1999 ◽  
Vol 29 (3) ◽  
pp. 339-346 ◽  
Author(s):  
M A Arthur ◽  
T G Siccama ◽  
R D Yanai
Keyword(s):  
Sugar Maple ◽  
Abies Balsamea ◽  
Fagus Grandifolia ◽  
Hardwood Forest ◽  
Northern Hardwood Forest ◽  
Betula Alleghaniensis ◽  
Forest Species ◽  
White Birch ◽  
Yellow Birch ◽  
Northern Hardwood

Improving estimates of the nutrient content of boles in forest ecosystems requires more information on how the chemistry of wood varies with characteristics of the tree and site. We examined Ca and Mg concentrations in wood at the Hubbard Brook Experimental Forest. Species examined were the dominant tree species of the northern hardwood forest and the spruce-fir forest. The concentrations of Ca and Mg, respectively, in lightwood of these species, mass weighted by elevation, were 661 and 145 µg/g for sugar maple (Acer saccharum Marsh.), 664 and 140 µg/g for American beech (Fagus grandifolia Ehrh.), 515 and 93 µg/g for yellow birch (Betula alleghaniensis Britt.), 525 and 70 µg/g for red spruce (Picea rubens Sarg.), 555 and 118 µg/g for balsam fir (Abies balsamea (L.) Mill.), and 393 and 101 µg/g for white birch (Betula papyrifera Marsh.). There were significant patterns in Ca and Mg concentrations with wood age. The size of the tree was not an important source of variation. Beech showed significantly greater concentrations of both Ca (30%) and Mg (33%) in trees growing in moist sites relative to drier sites; sugar maple and yellow birch were less sensitive to mesotopography. In addition to species differences in lightwood chemistry, Ca and Mg concentrations in wood decreased with increasing elevation, coinciding with a pattern of decreasing Ca and Mg in the forest floor. Differences in Ca and Mg concentration in lightwood accounted for by elevation ranged from 12 to 23% for Ca and 16 to 30% for Mg for the three northern hardwood species. At the ecosystem scale, the magnitude of the elevational effect on lightwood chemistry, weighted by species, amounts to 18% of lightwood Ca in the watershed and 24% of lightwood Mg but only 2% of aboveground biomass Ca and 7% of aboveground Mg.

scholarly journals Validation and refinement of allometric equations for roots of northern hardwoods

2007 ◽  
Vol 37 (9) ◽  
pp. 1777-1783 ◽  
Author(s):  
Matthew A. Vadeboncoeur ◽  
Steven P. Hamburg ◽  
Ruth D. Yanai
Keyword(s):  
Sugar Maple ◽  
Lateral Roots ◽  
Fagus Grandifolia ◽  
Allometric Equations ◽  
Hardwood Forest ◽  
Northern Hardwood Forest ◽  
Sampling Effort ◽  
Betula Alleghaniensis ◽  
Northern Hardwood ◽  
Mean Error

The allometric equations developed by Whittaker et al. (1974. Ecol. Monogr. 44: 233–252) at the Hubbard Brook Experimental Forest have been used to estimate biomass and productivity in northern hardwood forest systems for over three decades. Few other species-specific allometric estimates of belowground biomass are available because of the difficulty in collecting the data, and such equations are rarely validated. Using previously unpublished data from Whittaker’s sampling effort, we extended the equations to predict the root crown and lateral root components for the three dominant species of the northern hardwood forest: American beech ( Fagus grandifolia Ehrh.), yellow birch ( Betula alleghaniensis Britt), and sugar maple ( Acer saccharum Marsh.). We also refined the allometric models by eliminating the use of very small trees for which the original data were unreliable. We validated these new models of the relationship of tree diameter to the mass of root crowns and lateral roots using root mass data collected from 12 northern hardwood stands of varying age in central New Hampshire. These models provide accurate estimates of lateral roots (<10 cm diameter) in northern hardwood stands >20 years old (mean error 24%–32%). For the younger stands that we studied, allometric equations substantially underestimated observed root biomass (mean error >60%), presumably due to remnant mature root systems from harvested trees supporting young root-sprouted trees.

Allometric equations for young northern hardwoods: the importance of age-specific equations for estimating aboveground biomass

2011 ◽  
Vol 41 (4) ◽  
pp. 881-891 ◽  
Author(s):  
Farrah R. Fatemi ◽  
Ruth D. Yanai ◽  
Steven P. Hamburg ◽  
Matthew A. Vadeboncoeur ◽  
Mary A. Arthur ◽  
...  
Keyword(s):  
Aboveground Biomass ◽  
Acer Saccharum ◽  
Sugar Maple ◽  
Fagus Grandifolia ◽  
Stand Age ◽  
Betula Alleghaniensis ◽  
Yellow Birch ◽  
American Beech ◽  
Stem Wood ◽  
Northern Hardwood

Estimates of aboveground biomass and nutrient stocks are commonly derived using equations that describe tree dimensional relationships. Despite the widespread use of this approach, there is little information about whether equations specific to stand age are necessary for accurate biomass predictions. We developed equations for small trees (2–12 cm diameter) of six species in four young northern hardwood stands. We then compared our equations with equations used frequently in the literature that were developed in mature stands (Whittaker et al. 1974. Ecol. Monogr. 44: 233–252). Our equations for yellow birch ( Betula alleghaniensis Britt.) predicted 11%–120% greater stem wood for individual trees compared with the equations from Whittaker et al. and, on average, 50% greater aboveground yellow birch biomass in the four stands that we studied. Differences were less pronounced for sugar maple ( Acer saccharum Marsh.) and American beech ( Fagus grandifolia Ehrh.); our equations predicted, on average, 9% greater aboveground stand biomass for sugar maple and 3% lower biomass for American beech compared with Whittaker et al. Our results suggest that stand age may be an important factor influencing the aboveground allometry and biomass of small yellow birch trees in these developing northern hardwood stands.

American beech and sugar maple sapling relative abundance and growth are not modified by light availability following partial and total canopy disturbances

2015 ◽  
Vol 45 (6) ◽  
pp. 632-638 ◽  
Author(s):  
Kim Bannon ◽  
Sylvain Delagrange ◽  
Nicolas Bélanger ◽  
Christian Messier
Keyword(s):  
Soil Fertility ◽  
Acer Saccharum ◽  
Sugar Maple ◽  
Light Availability ◽  
Soil Nutrient ◽  
Fagus Grandifolia ◽  
American Beech ◽  
Clear Cutting ◽  
Canopy Opening ◽  
Unmanaged Forest

Studies have reported divergent results on the effect of soil fertility and canopy opening on understory density and growth of sugar maple (AS; Acer saccharum Marsh.) and American beech (FG; Fagus grandifolia Ehrh.). The main objective of this study was to evaluate the effect of a gradient of canopy opening and soil fertility on the density and growth of AS and FG saplings in southwestern Quebec, Canada. We investigated 56 stands containing both AS and FG that were subjected to different disturbance history types (DHTs) (UF, unmanaged forest; PC, partial cut; and CC, clearcut) on various soil types. AS and FG absolute and relative sapling density varied greatly among the 56 stands; however, no significant effects of DHT, soil nutrient availability, or their interaction were found. Both species responded positively in terms of radial growth to canopy openings, with FG growth being slightly better than AS growth in PC stands compared with other canopy treatments. Contrary to our hypothesis, AS did not show significantly higher growth than FG following clear-cutting. These results do not support the idea that AS abundance and growth could be promoted by increasing the intensity of the canopy opening during harvest, at least on the generally acidic and base-poor soils that were investigated.

scholarly journals Effects of Mechanical Site Preparation on the Abundance and Diversity of Ground-Layer Vegetation in Adirondack Northern Hardwood Stands

2007 ◽  
Vol 24 (1) ◽  
pp. 14-21 ◽  
Author(s):  
Jodi A. Forrester ◽  
Kimberly K. Bohn
Keyword(s):  
Acer Saccharum ◽  
Sugar Maple ◽  
Woody Species ◽  
Site Preparation ◽  
Fagus Grandifolia ◽  
Ground Layer ◽  
American Beech ◽  
Mechanical Site Preparation ◽  
Northern Hardwood ◽  
Fern Species

Abstract Forest management in northern hardwoods benefits from the use of site preparation treatments when the amount of American beech (Fagus grandifolia Ehrh.) and fern species in the understory interferes with regeneration of more desirable species, e.g., sugar maple (Acer saccharum Marshall). We assessed the cover and diversity of herbaceous and woody species in the ground layer of three Adirondack northern hardwood stands before and 3 years after a mechanical site preparation that removed all trees less than 14 cm with a brush saw. The treatment significantly increased the cover of all species cumulatively, with herbaceous, shrub, and arborescent species increasing significantly more in treated plots than in untreated plots. Sugar maple cover increased more in treated plots than in untreated plots, although American beech did as well. Species richness increased significantly more in treated plots than in untreated plots, but differences in diversity and evenness were not significantly different because of treatment after 3 years. Multivariate analysis indicated only minor changes in the plant community composition. Results show that mechanical site preparation techniques are a viable option for promoting abundance and maintaining diversity of the ground-layer vegetation in northern hardwood forests.

Long-term impact of liming on growth and vigor of northern hardwoods

2011 ◽  
Vol 41 (6) ◽  
pp. 1295-1307 ◽  
Author(s):  
Robert P. Long ◽  
Stephen B. Horsley ◽  
Thomas J. Hall
Keyword(s):  
Acer Saccharum ◽  
Sugar Maple ◽  
Keystone Species ◽  
Basal Area ◽  
Fagus Grandifolia ◽  
Northern Hardwood ◽  
Crown Health ◽  
Lime Application ◽  
Species Specific

Sugar maple (Acer saccharum Marsh.) is a keystone species in the northern hardwood forest, and decline episodes have negatively affected the growth and health of sugar maple in portions of its range over the past 50+ years. Crown health, growth, survival, and flower and seed production of sugar maple were negatively affected by a widespread decline event in the mid-1980s on the unglaciated Allegheny Plateau in northern Pennsylvania. A long-term liming study was initiated in 1985 to evaluate responses to a one-time application of 22.4 Mg·ha–1 of dolomitic limestone in four northern hardwood stands. Over the 23-year period ending in 2008, sugar maple basal area increment (BAINC) increased significantly (P ≤ 0.05) in limed plots from 1995 through 2008, whereas American beech (Fagus grandifolia Ehrh.) BAINC was unaffected. For black cherry (Prunus serotina Ehrh.), the third principal overstory species, BAINC and survival were reduced in limed plots compared with unlimed plots. Foliar Ca and Mg remained significantly higher in sugar maple foliage sampled 21 years after lime application, showing persistence of the lime effect. These results show long-term species-specific responses to lime application.

Growth and morphological responses of yellow birch, sugar maple, and beech seedlings growing under a natural light gradient

1998 ◽  
Vol 28 (7) ◽  
pp. 1007-1015 ◽  
Author(s):  
Marilou Beaudet ◽  
Christian Messier
Keyword(s):  
Leaf Area ◽  
Sugar Maple ◽  
Fagus Grandifolia ◽  
Stem Length ◽  
Betula Alleghaniensis ◽  
Yellow Birch ◽  
Morphological Response ◽  
Area Index ◽  
Light Gradient ◽  
Morphological Responses

Height and lateral growth, biomass distribution, leaf morphology, and crown architecture were studied in yellow birch (Betula alleghaniensis Britton), sugar maple (Acer saccharum Marsh.), and beech (Fagus grandifolia Ehrh.) seedlings growing under 1-50% of above-canopy light in a sugar maple stand, in Quebec. All three species showed increasing growth with increasing light, but growth of yellow birch was higher and more responsive than that of sugar maple and beech. All three species showed typical sun-shade morphological responses, such as decreasing specific leaf area and leaf area ratio, and increasing leaf area index, with increasing light availability. Sugar maple was morphologically more plastic than the other species. It showed variations in biomass allocation to leaves and branches, a decrease in branch length to seedling height ratio, and a marked increase in the ratio of leaf area to stem length. Although our results clearly demonstrate the ability of these three species to modify several of their morphological features in response to variations in light, they do not show a clear relationship between species shade tolerance and morphological response to light variations. We suggest that species-specific developmental patterns may act as important constraints to morphological acclimation to light variation.

Leaf- and plant-level carbon gain in yellow birch, sugar maple, and beech seedlings from contrasting forest light environments

2000 ◽  
Vol 30 (3) ◽  
pp. 390-404 ◽  
Author(s):  
Marilou Beaudet ◽  
Christian Messier ◽  
David W Hilbert ◽  
Ernest Lo ◽  
Zhang M Wang ◽  
...  
Keyword(s):  
Acer Saccharum ◽  
Sugar Maple ◽  
Light Availability ◽  
Fagus Grandifolia ◽  
Carbon Gain ◽  
Betula Alleghaniensis ◽  
Yellow Birch ◽  
Significant Difference ◽  
Leaf Level ◽  
Plant Level

Leaf-level photosynthetic-light response and plant-level daily carbon gain were estimated for seedlings of moderately shade-tolerant yellow birch (Betula alleghaniensis Britton) and shade-tolerant sugar maple (Acer saccharum Marsh.) and beech (Fagus grandifolia Ehrh.) growing in gaps and under a closed canopy in a sugar maple stand at Duchesnay, Que. All three species had a higher photosynthetic capacity (Amax) in the gaps than in shade, but yellow birch and beech responded more markedly than sugar maple to the increase in light availability. The high degree of plasticity observed in beech suggests that the prediction that photosynthetic plasticity should decrease with increasing shade tolerance may not hold when comparisons are made among a few late-successional species. Unit-area daily carbon gain (CA) was significantly higher in the gaps than in shade for all three species, but no significant difference was observed between light environments for plant-level carbon gain (CW). In shade, we found no difference of CA and CW among species. In gaps, beech had a significantly higher CA than sugar maple but similar to that of birch, and birch had a significantly higher CW than maple but similar to that of beech. Sugar maple consistently had lower carbon gains than yellow birch and beech but is nevertheless the dominant species at our study site. These results indicate that although plant-level carbon gain is presumably more closely related to growth and survival of a species than leaf-level photosynthesis, it is still many steps removed from the ecological success of a species.

Decomposition of aspen (Populustremuloides) leaf litter modified by leaching

1990 ◽  
Vol 20 (7) ◽  
pp. 943-951 ◽  
Author(s):  
William F. J. Parsons ◽  
Barry R. Taylor ◽  
Dennis Parkinson
Keyword(s):  
Mass Loss ◽  
Leaf Litter ◽  
Rocky Mountain ◽  
Exponential Model ◽  
Decay Rates ◽  
Double Exponential ◽  
Exponential Trend ◽  
Aspen Forest ◽  
Double Exponential Model ◽  
Soluble Material

In a Rocky Mountain aspen forest, the detailed pattern of mass loss from decomposing leaf litter of trembling aspen (Populustremuloides Michx.) during the first 6 months of decay was compared with that from aspen leaves modified to produce a more recalcitrant litter type by removal of leachable material (31.7% of original mass). Leaching litter removed substantial quantities of N (24%) and P (54%), but did not change the litter's C/N ratio (77:1); and leached leaves still contained 33% labile (benzene alcohol soluble) material. Decomposition of intact aspen litter was best described by a double exponential model (k1 = −7.91/year, k2 = −0.21/year), except during the first 2 weeks, when an extremely rapid mass loss (14.2%) apparently resulted from leaching. Microbial metabolism was probably responsible for most of the subsequent decay (35% total in 6 months). In contrast, decomposition of leached aspen showed no exponential trend and was best described by a simple linear regression with a slope of −19.7%/year. Additional data from a 2nd year (12–15 months decay) reduced the regression estimates of decay rates but did not alter the best fit models. Fits were improved slightly if temperature sum replaced time in the regressions, especially if 2nd-year data were included.

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