Genetic variation in basal area increment phenology and its correlation with growth rate in loblolly and slash pine families and clones

2006 ◽  
Vol 36 (4) ◽  
pp. 961-971 ◽  
Author(s):  
Veronica I Emhart ◽  
Timothy A Martin ◽  
Timothy L White ◽  
Dudley A Huber
Keyword(s):  
Growth Rate ◽  
Growth Traits ◽  
Negative Impact ◽  
Basal Area ◽  
Pinus Elliottii ◽  
Slash Pine ◽  
Basal Area Increment ◽  
Individual Tree ◽  
Basal Area Growth ◽  
Area Growth

We quantified basal area increment phenology over a 2-year period in one loblolly pine (Pinus taeda L.) and four slash pine (Pinus elliottii Engelm. var. elliottii) full-sib families propagated as rooting cuttings. In 2002, basal area growth started in March and stopped in October for both species, while in 2003, initiation and cessation occurred 2 weeks earlier for all families. In both years, peaks in basal area increment occurred in short (2–3 week) periods in the early spring for all families, followed by linear basal area growth until cessation. While there were significant size differences among taxa (species and families) at age 6 and 7 years, genetic differences in basal area growth rate were only expressed during short, discrete time periods primarily in the spring and fall. Basal area growth rate increased during periods when water soil availability increased (up to 300 mm), but an excess in water availability in the soil had a negative impact on growth. Within-family individual-tree broad-sense heritabilities ranged from 0.01 to 0.37 for all traits. In general, heritabilities were higher for growth traits than for phenological traits for all families. Both the strength and direction of correlation estimates of phenological traits with growth rate varied across families and years.

Experiments for alternative management of forest reserves: effects of partial cutting on stem growth and mortality of large oaks

2009 ◽  
Vol 39 (7) ◽  
pp. 1322-1330 ◽  
Author(s):  
Frank Götmark
Keyword(s):  
Growth Rate ◽  
Negative Impact ◽  
Canopy Cover ◽  
Basal Area ◽  
Canopy Openness ◽  
Partial Cutting ◽  
Basal Area Growth ◽  
Reference Plot ◽  
Protected Forests ◽  
Area Growth

Although protected forests are usually kept as free of human disturbance as possible, careful cutting may favour biodiversity in such areas. However, the use of heavy machinery during cutting operations may have a negative impact on protected forests. The large oaks ( Quercus spp.) found in many temperate nature reserves have a rich associated biodiversity. In 25 conservation forests in Sweden, the basal area growth and mortality of 250 large oaks (31–110 cm DBH) were compared between plots that were partially cut to promote the growth and survival of oaks and undisturbed plots. Each forest had one treatment plot (1 ha) and one undisturbed reference plot (1 ha) with similar levels of canopy cover. In 2002–2003, about 25% of the basal area was harvested in treatment plots, thereby increasing canopy openness from 14% to 33%. Cutting increased the mean relative basal area growth of large oaks (49% by plot, 22% by tree) after four seasons (P = 0.026). However, in nine forests, the growth rate was not higher in the treated plot than in the reference plot. Mortality, apparently due to cutting, was recorded only in one forest, where 18 large oaks died. Tree condition (percentage of dead large branches in crown) was the best (negative) predictor of growth rate, and openness around oak crown was also a (positive) predictor. Partial cutting favoured the growth of oaks and may be recommended, but a “hands-off” policy is also effective for these conservation forests.

A New Index Representing Individual Tree Competitive Status

1973 ◽  
Vol 3 (4) ◽  
pp. 495-500 ◽  
Author(s):  
James A. Moore ◽  
Carl A. Budelsky ◽  
Richard C. Schlesinger
Keyword(s):  
Spatial Distribution ◽  
Strong Correlation ◽  
Basal Area ◽  
Tree Size ◽  
Competition Index ◽  
Individual Tree ◽  
Silvicultural Practices ◽  
Basal Area Growth ◽  
Hardwood Species ◽  
Area Growth

A new competition index, modified Area Potentially Available (APA), was tested in a complex unevenaged stand composed of 19 different hardwood species. APA considers tree size, spatial distribution, and distance relationships in quantifying intertree competition and exhibits a strong correlation with individual tree basal area growth. The most important characteristic of APA is its potential for evaluating silvicultural practices.

scholarly journals An Individual-Tree Growth and Yield Prediction System for Uneven-Aged Shortleaf Pine Stands

2000 ◽  
Vol 24 (2) ◽  
pp. 112-120 ◽  
Author(s):  
Michael M. Huebschmann ◽  
Lawrence R. Gering ◽  
Thomas B. Lynch ◽  
Onesphore Bitoki ◽  
Paul A. Murphy
Keyword(s):  
Basal Area ◽  
Growth Patterns ◽  
Growth And Yield ◽  
Prediction System ◽  
Pinus Echinata ◽  
Shortleaf Pine ◽  
Individual Tree ◽  
Basal Area Growth ◽  
Area Growth ◽  
Pine Stands

Abstract A system of equations modeling the growth and development of uneven-aged shortleaf pine (Pinus echinata Mill.) stands is described. The prediction system consists of two main components: (1) a distance-independent, individual-tree simulator containing equations that forecast ingrowth, basal-area growth, probability of survival, total and merchantable heights, and total and merchantable volumes and weights of shortleaf pine trees; and (2) stand-level equations that predict hardwood ingrowth, basal-area growth, and mortality. These equations were combined into a computer simulation program that forecasts future states of uneven-aged shortleaf pine stands. Based on comparisons of observed and predicted stand conditions in shortleaf pine permanent forest inventory plots and examination of the growth patterns of hypothetical stands, the simulator makes acceptable forecasts of stand attributes. South. J. Appl. For. 24(2):112-120.

Individual-tree basal area growth models for jack pine and black spruce in northern Ontario

2004 ◽  
Vol 80 (3) ◽  
pp. 366-374 ◽  
Author(s):  
Lianjun Zhang ◽  
Changhui Peng ◽  
Qinglai Dang
Keyword(s):  
Tree Growth ◽  
Black Spruce ◽  
Basal Area ◽  
Jack Pine ◽  
Mixed Stands ◽  
Northern Ontario ◽  
Individual Tree ◽  
Basal Area Growth ◽  
Wide Range ◽  
Area Growth

Individual-tree models of five-year basal area growth were developed for jack pine (Pinus banksiana Lamb.) and black spruce (Picea mariana (Mill.) BSP) in northern Ontario. Tree growth data were collected from long-term permanent plots of pure and mixed stands of the two species. The models were fitted using mixed model methods due to correlated remeasurements of tree growth over time. Since the data covered a wide range of stand ages, stand conditions and tree sizes, serious heterogeneous variances existed in the data. Therefore, the coefficients of the final models were obtained using weighted regression techniques. The models for the two species were evaluated across 4-cm diameter classes using independent data. The results indicated (1) the models of jack pine and black spruce produced similar prediction errors and biases for intermediate-sized trees (12–28 cm in tree diameter), (2) both models yielded relatively large errors and biases for larger trees (> 28 cm) than those for smaller trees, and (3) the jack pine model produced much larger errors and biases for small-sized trees (< 12 cm) than did the black spruce model. Key words: mixed models, repeated measures, model validation

Individual tree basal-area growth parameter estimates for four models

2004 ◽  
Vol 174 (1-2) ◽  
pp. 115-126 ◽  
Author(s):  
J.J Colbert ◽  
Michael Schuckers ◽  
Desta Fekedulegn ◽  
James Rentch ◽  
Máirtı́n MacSiúrtáin ◽  
...  
Keyword(s):  
Growth Parameter ◽  
Basal Area ◽  
Parameter Estimates ◽  
Individual Tree ◽  
Basal Area Growth ◽  
Area Growth

scholarly journals Species Mixing Effects on Height–Diameter and Basal Area Increment Models for Scots Pine and Maritime Pine

Forests ◽  
2019 ◽  
Vol 10 (3) ◽  
pp. 249 ◽  
Author(s):  
José Riofrío ◽  
Miren del Río ◽  
Douglas Maguire ◽  
Felipe Bravo
Keyword(s):  
Scots Pine ◽  
Tree Growth ◽  
Growth Models ◽  
Basal Area ◽  
Maritime Pine ◽  
Basal Area Increment ◽  
Mixing Effects ◽  
Basal Area Growth ◽  
Area Growth ◽  
Species Mixtures

Models that incorporate known species-mixing effects on tree growth are essential tools to properly design silvicultural guidelines for mixed-species stands. Here, we developed generalized height–diameter (h-d) and basal area growth models for mixed stands of two main forest species in Spain: Scots pine (Pinus sylvestris L.) and Maritime pine (Pinus pinaster Ait.). Mixed-effects models were fitted from plot measurement and tree rings data from 726 Scots pine and 693 Maritime pine trees from mixed and pure stands in the Northern Iberian Range in Spain, with the primary objective of representing interactions between the species where they are interspersed in mixtures of varying proportions. An independent dataset was used to test the performance of the h-d models against models previously fitted for monospecific stands of both species. Basal area increment models were evaluated using a 10-fold block cross-validation procedure. We found that species mixing had contrasting effects on the species in both models. In h-d models, the species-mixing proportion determined the effect of species interactions. Basal area growth models showed that interspecific competition was influential only for Maritime pine; however, these effects differed depending on the mode of competition. For Scots pine, tree growth was not restricted by interspecies competition. The combination of mixed-effect models and the inclusion of parameters expressing species-mixing enhanced estimates of tree height and basal area growth compared with the available models previously developed for pure stands. Although the species-mixing effects were successfully represented in the fitted models, additional model components for accurately simulating the stand dynamics of mixtures with Scots pine and Maritime pine and other species mixtures require similar model refinements. Upon the completion of analyses required for these model refinements, the degree of improvement in simulating growth in species mixtures, including the effects of different management options, can be evaluated.

An individual-tree basal area growth model for black spruce in second-growth peatland stands

1999 ◽  
Vol 29 (5) ◽  
pp. 621-629 ◽  
Author(s):  
Hannu Hökkä ◽  
Arthur Groot
Keyword(s):  
Growth Model ◽  
Black Spruce ◽  
Basal Area ◽  
Random Parameter ◽  
Considerable Change ◽  
Tree Level ◽  
Individual Tree ◽  
Basal Area Growth ◽  
Second Growth ◽  
Area Growth

A basal area growth model was developed to predict the growth of individual trees in second-growth black spruce (Picea mariana (Mill.) BSP) stands on northeastern Ontario peatlands. The data were derived from stem analysis trees collected in 1985 and 1986 from stands harvested 47-68 years earlier. For a period starting from the date of data collection and going back to 10 years from the harvesting, tree basal area growth, diameters, and stand characteristics were retrospectively calculated at 5-year intervals. To estimate previous mortality, self-thinning relationships for black spruce were applied. In the model, 5-year basal area growth of a tree was expressed as a function of tree diameter, stand-level competition, tree-level competition, and peat thickness. There was considerable change in the growth-size relationship over time. A random parameter approach was applied in model construction to account for the spatial and temporal correlations of the observations. The proposed model explicitly incorporates factors normally included in a "random error" term and, therefore, should provide more sensitive tests of the contributions of the various factors to growth prediction. The estimated model showed only slight bias against the modeling data and the predicted stand basal area development was comparable with that given in other studies.

An individual-tree basal area growth model for loblolly pine stands

1996 ◽  
Vol 26 (2) ◽  
pp. 327-331 ◽  
Author(s):  
Paul A. Murphy ◽  
Michael G. Shelton
Keyword(s):  
Loblolly Pine ◽  
Basal Area ◽  
Growth Function ◽  
Logistic Function ◽  
Growth Patterns ◽  
Potential Growth ◽  
Individual Tree ◽  
Basal Area Growth ◽  
Area Growth ◽  
Using Data

Tree basal area growth has been modeled as a combination of a potential growth function and a modifier function, in which the potential function is fitted separately from open-grown tree data or a subset of the data and the modifier function includes stand and site variables. We propose a modification of this by simultaneously fitting both a growth component and a modifier component. The growth component can be any function that approximates tree growth patterns, and the logistic function is chosen as the modifier component. This approach can be adapted to a variety of stand conditions, and its application is demonstrated using data from an uneven-aged loblolly pine (Pinustaeda L.) study located in Arkansas and Louisiana.

scholarly journals Coupe préparatoire et croissance en surface terrière d'une sapiniére de seconde venue à la forêt modèle du Bas-Saint-Laurent, Québec

2001 ◽  
Vol 77 (4) ◽  
pp. 685-695 ◽  
Author(s):  
Richard Zarnovican ◽  
Jean-Martin Lussier ◽  
Claude Laberge
Keyword(s):  
Growth Rate ◽  
Relative Size ◽  
Basal Area ◽  
Balsam Fir ◽  
Basal Area Growth ◽  
Periodic Growth ◽  
Area Growth ◽  
Crown Characteristics ◽  
Highly Correlated ◽  
The Impact

Balsam fir basal area growth was studied 5 years after the preparatory cut in the context of natural regeneration by the shelterwood system. The study was carried out in a 60-year-old second-growth balsam fir-yellow birch stand. The felling trials were realized in 16 plots and consisted of control and three felling regimes (15, 30 and 45% of removed basal area). The periodic (5 years) mean growth rate on dbh of trees in plots varies between 6 and 12% in response to felling intensity. The basal area of plots presents a mean periodic growth rate of 7.4% independently of felling intensity. There are highly significant correlations between the live crown characteristics and periodic basal area growth. This growth is highly correlated with inital diameter and intensity of felling. The trees of higher relative size are more productive than the others and the impact of felling on periodic basal area growth is significant when the intensity of felling is greater than 30%. Conversely, the ratio between periodic basal area growth after treatment and periodic basal area growth before treatment is correlated only with the intensity of felling. Finally, intensity of felling had no effect on periodic basal area growth per square meter of crown projected area. Key words: preparatory felling, basal area growth, balsam fir

Growth responses to commercial thinning in Douglas-fir stands with varying severity of Swiss needle cast in Oregon, USA

2005 ◽  
Vol 35 (10) ◽  
pp. 2394-2402 ◽  
Author(s):  
Douglas B Mainwaring ◽  
Douglas A Maguire ◽  
Alan Kanaskie ◽  
Jeff Brandt
Keyword(s):  
Basal Area ◽  
Douglas Fir ◽  
Growth Responses ◽  
Infection Level ◽  
Individual Tree ◽  
Needle Cast ◽  
Commercial Thinning ◽  
Basal Area Growth ◽  
Area Growth ◽  
Swiss Needle Cast

Concern has risen about the degree to which Douglas-fir (Pseudotsuga menziesii (Mirb.) Franco) stands with severe infections of Swiss needle cast (SNC) respond to thinning. A retrospective study was established in the fall of 2001 to assess the growth of Douglas-fir stands that were commercially thinned between 4 and 10 years ago. Current SNC infection levels in these stands ranged from severe to very light. Past volume and basal area growth declined with increasing severity of SNC, as measured by current foliage retention and crown length / sapwood ratio. As has been observed in many other studies, thinning to lower residual stock reduced stand level growth; however, individual tree growth increased with lower residual stand density. The ratio of growth in successive periods and analysis of annual basal area growth since thinning suggested that trees did respond to thinning, although less so as SNC increased. A positive response to thinning, regardless of infection level, was confirmed by an analysis of annual trends in basal area growth over the first 5 years after thinning.

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