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Évaluation visuelle des arbres feuillus sur pied et
valeur des produits transformés
Thèse
Filip Havreljuk
Doctorat en sciences forestières
Philosophiae doctor (Ph.D.)
Québec, Canada
© Filip Havreljuk, 2015
iii
Résumé
Les forêts feuillues tempérées du sud du Québec ont une grande importance économique, car
elles sont la principale source d’approvisionnement des industries des produits d'apparence
en bois. Toutefois, la difficulté de relier l’apparence externe d’un arbre à la qualité interne de
son bois engendre des incertitudes liées à l’approvisionnement, puisque la qualité des bois
sélectionnés pour la récolte peut ne pas correspondre aux besoins réels des usines de
transformation. L’objectif principal de ce projet était d’améliorer les prévisions des
caractéristiques des approvisionnements de bois feuillu en reliant l’évaluation de la qualité
des arbres sur pied à la composition du panier de produits transformés et à sa valeur
monétaire. Un des facteurs internes qui affecte la valeur des sciages d’érable à sucre (Acer
saccharum Marsh.) et de bouleau jaune (Betula alleghaniensis Britt.) est la présence d’une
zone de couleur brun-rougeâtre au centre de la tige, appelée coloration de cœur. Un
échantillonnage dans 12 localisations de la zone tempérée du sud du Québec a montré que
les différences régionales de la proportion radiale de la zone colorée chez ces deux espèces
étaient principalement attribuables à des facteurs liés au développement des arbres, tels que
l’âge et les accroissements autour de la zone colorée. Une partie de la variabilité chez l’érable
à sucre était aussi associée à la température minimale annuelle d'une localisation. Par ailleurs,
l’étude de 64 érables à sucre et 32 bouleaux jaunes abattus, tronçonnés et sciés en planches
a mis en évidence le fait que parmi tous les types de défaut qui doivent être pris en
considération lors du marquage des arbres, les signes visibles d’infection fongique et les
fentes avaient la plus grande influence négative sur la valeur des deux espèces. L’analyse des
sciages a montré que la proportion des meilleurs grades augmentait avec la longueur et le
diamètre des billes, ce qui fait qu’elle était plus élevée dans le bas de l’arbre. Les billes
présentant une grande zone colorée ont produit davantage de bois de moindre valeur. Dans
leur ensemble, ces résultats permettent d’établir des liens entre le classement visuel des arbres
sur pied et la qualité de produits transformés permettant une meilleure prise de décisions liée
à l’approvisionnement en bois feuillu.
v
Abstract
Temperate deciduous forests of southern Quebec are of great economic importance because
they are the main supply source of the appearance wood products industries. However, the
difficulty of linking the external characteristics of a tree to the internal quality of its wood
creates supply-related uncertainties, since the quality of selected trees for harvest may not
correspond to the real needs of these processing industries. The main objective of this study
was to improve the supply forecasts of hardwood processing industries by linking the quality
assessment of standing trees to their products assortment and their monetary value. One of
the most important internal factors affecting the value of sugar maple (Acer saccharum
Marsh.) and yellow birch (Betula alleghaniensis Britt.) lumber is the presence of a reddish-
brown colored area in the center of the stem called red heartwood. Samples from 12 locations
throughout the temperate zone in southern Quebec showed that regional differences in the
radial proportion of the colored area in both species were mainly due to factors related to tree
development, such as age and radial growth around the colored area. Part of the variability
in sugar maple was also associated with the annual minimum temperature of a sampling
location. In addition, the study of 64 sugar maple and 32 yellow birch trees that were
harvested, bucked into logs and processed into lumber showed that among all defect types
that need to be considered for tree marking, visible evidence of fungal infections and cracks
had the largest negative influence on value in both species. The analysis of the lumber
products assortment showed that the proportion of the best grades increased with the length
and the diameter of the logs, so that it was higher at the bottom of the stem. Logs with a large
red heartwood area produced more wood of lesser value. Overall, these results link the visual
assessment of standing trees to the quality and value of processed products to allow better
decision making in the hardwoods supply chain.
vii
Table des matières
Résumé .................................................................................................................................. iii
Abstract ................................................................................................................................... v
Table des matières ............................................................................................................... vii
Liste des tableaux ................................................................................................................... ix
Liste des figures ..................................................................................................................... xi
Remerciements .................................................................................................................... xiii
Avant-propos ..................................................................................................................... xvii
Introduction générale .............................................................................................................. 1
Démarche méthodologique .............................................................................................. 6
Chapitre 1 Regional variation in the proportion of red heartwood in sugar maple and
yellow birch ......................................................................................................................... 9
Abstract .......................................................................................................................... 10
Résumé .......................................................................................................................... 11
Introduction ................................................................................................................... 12
Materials and methods ................................................................................................... 14
Results ........................................................................................................................... 21
Discussion ...................................................................................................................... 26
Conclusion ..................................................................................................................... 30
Acknowledgments ......................................................................................................... 31
Chapitre 2 Integrating standing value estimations into tree marking guidelines to meet
wood supply objectives ..................................................................................................... 33
Abstract .......................................................................................................................... 34
Résumé .......................................................................................................................... 35
Introduction ................................................................................................................... 36
Material and methods .................................................................................................... 38
Results ........................................................................................................................... 47
Discussion ...................................................................................................................... 54
Conclusion ..................................................................................................................... 57
Acknowledgements ....................................................................................................... 58
viii
Chapitre 3 Predicting lumber grade occurrence and volume recovery in sugar maple and
yellow birch logs .............................................................................................................. 59
Abstract ......................................................................................................................... 60
Résumé .......................................................................................................................... 61
Introduction ................................................................................................................... 62
Material and methods .................................................................................................... 64
Results ........................................................................................................................... 73
Discussion ..................................................................................................................... 83
Conclusion .................................................................................................................... 87
Acknowledgements ....................................................................................................... 87
Conclusion générale ............................................................................................................. 89
Bibliographie ........................................................................................................................ 95
Annexe 1 : Données utilisées pour le chapitre 1 ................................................................ 109
Annexe 2 : Données utilisées pour les chapitres 2 et 3 ...................................................... 113
ix
Liste des tableaux
Table 1.1 Summary of sampling locations used in the study. .............................................. 15
Table 1.2 Mean sample tree characteristics. SD is the standard deviation. .......................... 16
Table 1.3 List of explanatory variables screened in the modeling process. ......................... 20
Table 1.4 Comparison of the multiple linear regression models for sugar maple red
heartwood proportion (RHP). ............................................................................................... 24
Table 1.5 Parameter estimates and their standard errors (±SE) for the final models. .......... 25
Table 1.6 Comparison of the multiple linear regression models for yellow birch red
heartwood proportion (RHP). ............................................................................................... 26
Table 2.1 Mean sample tree characteristics for the sugar maple and yellow birch data. ..... 41
Table 2.2 Lumber grade distribution among the sawn boards. ............................................. 44
Table 2.3 Distribution of NHLA grades among tree quality classes. ................................... 44
Table 2.4 Mean sugar maple and yellow birch lumber values from 2008 to 2012. ............. 45
Table 2.5 Proportion of study trees (%) affected by a given defect category. ...................... 50
Table 2.6 Parameter estimates (± SE) and p-values for the model including DBH, fungal
infections, and cracks given by eq. (3). ................................................................................ 50
Table 2.7 Comparison of the linearized models for predicting the value per unit volume
(VAL) of each stem. ............................................................................................................. 52
Table 3.1 Mean log characteristics for the sugar maple and yellow birch data. ................... 65
Table 3.2 Lumber grade distribution among the sawn boards. ............................................. 67
Table 3.3 Mean sugar maple and yellow birch lumber values from 2008 to 2012. ............. 72
Table 3.4 Proportion of NHLA lumber grades and colors among log grades. ..................... 73
Table 3.5 List of models predicting the VRG of sugar maple and yellow birch. .................. 74
Table 3.6 Parameter estimates (and standard errors) for the best model to predicting VRG
(model 8). .............................................................................................................................. 76
Table 3.7 List of models predicting the VRC of sugar maple. .............................................. 78
Table 3.8 List of models predicting the VRC of yellow birch. ............................................. 79
Table 3.9 Parameter estimates (and standar errors) for the best model to predicting VRC of
sugar maple (model 4) and yellow birch (9). ........................................................................ 81
xi
Liste des figures
Figure 1.1 Location of the sampling regions across Québec. ............................................... 14
Figure 1.2 Illustration of the red heartwood separation procedure performed using ImageJ.
(A) Initial image. (B) The resulting image after applying the threshold function. (C) The
final image after the noise from the threshold function was removed. ................................. 17
Figure 1.3 Mean red heartwood proportion (RHP) for sugar maple and yellow birch in the
12 sampling regions. Two study sites are included in each region and eight trees were
sampled from each site. Error bars represent standard errors. .............................................. 21
Figure 1.4 Mean red heartwood proportion (RHP) for sugar maple and yellow birch across
bioclimatic subdomains. Eastern Balsam fir – Yellow birch subdomain (n = 92), Western
Balsam fir – Yellow birch subdomain (n = 64), Eastern Sugar maple – Yellow birch
subdomain (n = 92), and Western Sugar maple – Yellow birch subdomain (n = 128). Error
bars represent standard errors. .............................................................................................. 22
Figure 1.5 Number of discoloured wood rings as a function of the total number of rings at
1.3 m. .................................................................................................................................... 23
Figure 1.6 Model-averaged predictions and unconditional 95% confidence intervals for the
best-fit model parameters for sugar maple. ........................................................................... 24
Figure 1.7 Model-averaged predictions and unconditional 95% confidence intervals for the
best-fit model parameters for yellow birch. .......................................................................... 26
Figure 2.1 Location of the study areas. ................................................................................. 38
Figure 2.2 Predicted VAL (US$·m−3) in relation to vigor classification. Trees are classified
by harvest priorities: moribund trees (M), surviving trees (S), growing trees to be conserved
(C), and reserve stock trees (R) (Boulet 2007). .................................................................... 48
Figure 2.3 Predicted VAL (US$·m−3) in relation to quality classification. The four grades
(A, B, C, and D) are used to describe the potential for sawlog production, with grade A
being the highest and grade D the lowest (i.e., trees with no sawlog potential) (Monger
1991). .................................................................................................................................... 49
Figure 2.4 Predicted VAL (US$·m−3) of sugar maple and yellow birch in relation to the
presence of the main tree defects. ......................................................................................... 51
Figure 2.5 Predicted VAL (US$·m−3) in relation with sound wood depth for quality
classification (Monger 1991). ............................................................................................... 53
Figure 2.6 Predicted VAL (US$·m−3) in relation with sound wood depth for main defects.
.............................................................................................................................................. 53
Figure 3.1 Observed (bars) versus predicted (points) frequencies of the lumber volume
recovery of lumber grades (VRG). ........................................................................................ 68
xii
Figure 3.2 Observed (bars) versus predicted (points) frequencies of the lumber volume
recovery of the lumber colors (VRC). ................................................................................... 69
Figure 3.3 Predicted lumber volume recovery for each lumber grade (VRG) plotted against
the small-end diameter of the log (cm) of the best model (model 8). Lines represent loess
smoothing functions with standard error through the predictions. ....................................... 75
Figure 3.4 Predicted lumber volume recovery for each color category (VRC) plotted against
the covariates of the best model for sugar maple (model 4). Lines represent loess smoothing
functions with standard error through the predictions. ........................................................ 80
Figure 3.5 Predicted lumber volume recovery for each color category (VRC) plotted against
the covariates of the best model for yellow birch (model 9). Lines represent loess
smoothing functions with standard error through the predictions. ....................................... 80
Figure 3.6 Predicted value recovery against log net volume established from the predicted
VRG (model 8). Lines represent linear smoothing functions with standard error plotted
against the observed value recovery. .................................................................................... 83
xiii
Remerciements
Ce doctorat n’aurait pas été possible sans la contribution financière du Fonds de recherche
du Québec – Nature et technologies (FRQNT) qui m’a accordé une bourse et qui a financé
ce projet de recherche. Je tiens à remercier cet organisme pour sa confiance et son appui.
Ce fut un privilège de pouvoir travailler avec mon directeur de recherche et véritable mentor,
Alexis Achim, qui a toujours eu confiance en moi et qui a été le premier à me donner la
chance de poursuivre mes études graduées sur un sujet qui me passionne. Il a toujours été
disponible pour m’aider à avancer dans mon projet et faire de moi un meilleur chercheur.
J’aimerais aussi remercier mon codirecteur de recherche, David Pothier, pour sa
disponibilité, ses commentaires constructifs et sa rigueur qui ont permis de mener à terme ce
projet. Merci Alexis et David pour l’opportunité que vous m’avez donnée, par votre
encadrement et votre support dans mes travaux, autant du point de vue logistique, financier
et scientifique, que moral avec votre sens d’humour!
J’aimerais aussi remercier du fond du cœur tous mes assistantes et assistants de terrain et de
laboratoire : Amélie Denoncourt, Élisabeth Dubé, Frauke Lenz, Marine Bouvier, Julia
Maman, Stéphanie Cloutier, Marie-Pier Arsenault et Louis Gauthier. La motivation, l’énergie
et la bonne volonté que vous avez mise dans votre travail m’ont aidé à mener à terme ce
projet. J’ai eu beaucoup de plaisir à travailler avec vous. Merci également à mes collègues et
amis qui m’ont aidé au cours du projet : Julie Barrette, Simon Delisle-Boulianne, Emmanuel
Duchateau, Louis-Vincent Gagné, Normand Paradis et Charles Ward.
Un grand merci aussi aux personnes suivantes pour leur soutien scientifique à travers mon
doctorat: David Auty (analyses statistiques et révisions linguistiques des textes), Marc J.
Mazerolle (conseils en statistiques et programmation), Ann Delwaide (aide en
dendrochronologie), Rémi St-Amant et Jacques Régnière (aide avec BioSIM et l’analyse des
données météorologiques), Jean McDonald (conseils en transformation des feuillus), Martine
Lapointe et Jean-Philippe Gagnon (aide sur le terrain) et S.Y. Zhang (pour ses idées
originales qui ont permis d’orienter le projet de recherche).
xiv
Un projet de cette envergure n’aurait pas été possible sans la participation de nombreux
partenaires industriels qui ont collaboré aux différents volets du projet de recherche
permettant ainsi d’augmenter la portée de cette étude. J’aimerais remercier Steve Bédard,
François Guillemette ainsi que leur équipe de la Direction de la recherche forestière du
Ministère des Forêts, de la Faune et des Parcs du Québec pour leur appui et leur collaboration
au projet de recherche. De plus, mes sincères remerciements vont au Centre de recherche sur
les matériaux renouvelables (CRMR), à la Coopérative Forestière des Hautes-Laurentides
(CFHL), à l’École de foresterie et de technologie du bois de Duchesnay, au Groupement
forestier de Portneuf, au Ministère des Forêts, de la Faune et des Parcs (MFFP), à la Station
touristique de Duchesnay (SÉPAQ) et à FPInnovations. Merci infiniment à toutes les
personnes de ces organismes qui ont collaboré de près ou de loin à cette étude.
Merci au Centre d’étude de la forêt (CEF) pour le financement des formations de
perfectionnement et des conférences auxquelles j’ai participé tout au long de mon projet de
recherche. Merci à Malcolm Cecil-Cockwell et John Caspersen pour leur accueil à
l’Université de Toronto et à la forêt de Haliburton lors de l’été 2011. Ce séjour fut très
agréable et formateur.
J’aimerais aussi remercier les membres de mon comité de thèse qui ont accepté d’examiner
ce document : Julie Cool, Ph.D. (The University of British Columbia), Myriam Drouin, Ph.D.
(FPInnovations) et Robert Beauregard, Ph.D. (Université Laval).
Je tiens à remercier particulièrement mes trois collègues de bureau et biologistes préférés,
Kaysandra Waldron, Emmanuel Duchateau et Sébastien Lavoie. Que ce soit pour parler du
travail, boire une bière ou socialiser, j’ai adoré vous côtoyer et vous avez rendu mes études
plus agréables.
Merci à tous mes autres amis avec qui j’ai pu passer de bons moments tout au long de mes
études : Anne Allard-Duchêne, Juliette Boiffin, Geneviève Bourgeois, Robin Colette, Joanie
Couture, Roxane Hamel St-Laurent, Étienne Hubert-Legault, Antoine Marcoux, Édith
Lachance, Claude Lefrançois, Pierre-Étienne Messier, Sacha Nandlall, Caroline Plante,
Mylène Savard, Annie-Claude Taillon, Valérie Packwood-Vignet et Célia Ventura-Giroux.
xv
Enfin, je veux remercier mes parents et ma famille qui m’ont toujours appuyé dans mon
cheminement. Leur support inconditionnel est à la source de ma réussite.
Je garde un excellent souvenir de ces dernières années et je remercie du fond du cœur tous
ceux et celles qui y ont contribué. Merci!
xvii
Avant-propos
Insertion d’articles
La présente thèse est composée de trois chapitres rédigés en anglais et présentés sous forme
d’articles scientifiques dont je suis le premier auteur. En tant que candidat au doctorat, j'ai
effectué une revue de littérature sur le sujet de recherche, établi les objectifs et les hypothèses
de recherche, planifié et réalisé l'échantillonnage sur le terrain, réalisé les analyses
statistiques et l’interprétation des résultats et rédigé l’ensemble de la thèse et des articles
scientifiques qui y sont rattachés.
Chapitre 1
Havreljuk, F., Achim, A. and Pothier, D. 2013. Regional variation in the proportion of red
heartwood in sugar maple and yellow birch. Can. J. For. Res. 43(3), 278–287.
doi:10.1139/cjfr-2012-0479
Chapitre 2
Havreljuk, F., Achim, A., Auty, D., Bédard, S. and Pothier, D. 2014. Integrating standing
value estimations into tree marking guidelines to meet wood supply objectives. Can. J.
For. Res. 44(7), 750–759. doi: 10.1139/cjfr-2013-0407
Chapitre 3
Havreljuk, F., Achim, A. and Pothier, D. Predicting lumber grade occurrence and volume
recovery in sugar maple and yellow birch logs. L’article sera soumis sous peu.
Les données brutes ayant servi à la réalisation de cette thèse ont été ajoutées sous forme de
sommaires en annexe du document.
Coauteurs des chapitres
La rédaction de cette thèse de doctorat a été encadrée par Alexis Achim et David Pothier,
mon directeur et mon codirecteur de thèse, respectivement. Ils sont les coauteurs de tous les
chapitres puisqu’ils ont supervisé les travaux de recherche, m’ont conseillé et ont bonifié les
xviii
articles scientifiques. David Auty est le coauteur du second chapitre puisqu’il a participé aux
analyses statistiques et à la révision grammaticale du texte. Steve Bédard est également
coauteur du second chapitre car une partie de l’étude a pu être réalisée dans un dispositif de
recherche du Ministère des Forêts, de la Faune et des Parcs du Québec sous sa responsabilité.
Il a également apporté ses révisions au manuscrit.
Alexis Achim : Département des sciences du bois et de la forêt, Université Laval, 2405
rue de la Terrasse, Québec, Québec, Canada. G1V 0A6.
Courriel : [email protected]
David Pothier : Département des sciences du bois et de la forêt, Université Laval, 2405
rue de la Terrasse, Québec, Québec, Canada. G1V 0A6.
Courriel : [email protected]
David Auty : School of Forestry, Northern Arizona University, 200 East Pine Knoll
Drive, PO Box: 15018, Flagstaff, Arizona, USA. AZ 86011.
Courriel : [email protected]
Steve Bédard : Direction de la recherche forestière, Ministère des Forêts, de la Faune et
des Parcs du Québec, 2700 rue Einstein, Québec, Québec, Canada. G1P 3W8.
Courriel : [email protected]
Diffusion des résultats
Il est à noter que les résultats présentés dans cette thèse ont été diffusés lors des conférences
suivantes :
Havreljuk, F., Achim, A., Auty, D., Bédard, S. and Pothier, D. 2014. Integrating standing
value estimations into tree marking guidelines to meet wood supply objectives. 7è
Congrès Est du Canada et États-Unis d’Amérique en sciences forestières (eCANUSA).
Rimouski, Québec. 16-18 octobre 2014.
xix
Havreljuk, F., Achim, A. and Pothier, D. 2013. Variation régionale de la coloration de
cœur chez l’érable à sucre et le bouleau jaune. Colloque du CEF (Centre d’étude de la
forêt). Montebello, Québec, Canada. 24 avril 2013.
Havreljuk, F., Achim, A. and Pothier, D. 2012. Variation régionale de la coloration de
cœur chez l’érable à sucre et le bouleau jaune. Colloque III (FOR-8001). Université
Laval, Québec. 27 novembre 2012.
Havreljuk, F., Achim, A. and Pothier, D. 2012. Distribution régionale de la coloration
de cœur chez l’érable à sucre et le bouleau jaune. Colloque facultaire FFGG, Université
Laval, Québec. 15 novembre 2012.
Havreljuk, F., Achim, A. and Pothier, D. 2011. Peut-on ramener des considérations pour
la qualité du bois dans nos stratégies sylvicoles en forêt feuillue ? Journée du CRB
(Centre de recherche sur le bois), Université Laval, Québec, Canada. 25 novembre 2011.
Havreljuk, F., Achim, A. and Pothier, D. 2011. Integrating Standing Value Estimations
into Québec's Tree Marking System for Hardwoods. International Scientific Conference
on Hardwood Processing (ISCHP 3), Virginia Tech, Blacksburg, VA, USA.
http://woodproducts.sbio.vt.edu/ischp2011/index.php. October 17, 2011.
Havreljuk, F., Achim, A. and Pothier, D. 2010. Distribution régionale de la coloration
de cœur de l’érable à sucre. Journée du CRB (Centre de recherche sur le bois), Université
Laval, Québec, Canada. 26 novembre 2010.
Havreljuk, F., Achim, A. and Pothier, D. 2010. Distribution régionale de la coloration
de cœur de l’érable à sucre. Colloque du CEF (Centre d’étude de la forêt), Orford,
Québec, Canada. 14 mars 2010.
1
Introduction générale
Les forêts feuillues du sud du Québec ont une grande importance économique en raison de
leurs utilisations multiples, de la valeur de leurs bois et de la proximité des usines de
transformation et des marchés. Les principales espèces utilisées par l’industrie des feuillus
durs sont l’érable à sucre (Acer saccharum Marsh.) et le bouleau jaune (Betula alleghaniensis
Britt.) (MRNFPQ et CRIQ 2003; MRNFQ et CRIQ 2007). Entre 2008 et 2012, la
consommation totale de feuillus durs par les secteurs de transformation primaire du
déroulage, du sciage, des panneaux, des pâtes et papiers et du bois de chauffage était en
moyenne de 6 461 000 m³ (MRNQ 2013). Toutefois, cette industrie a dû composer avec un
contexte économique défavorable, ce qui a contribué à ralentir les activités de ce secteur ces
dernières années. D’ailleurs, durant cette période, la récolte des feuillus dans les forêts
publiques et privées du Québec ne s’est élevée qu’au tiers de la possibilité forestière totale
(CIFQ 2008, 2012).
Outre les problèmes associés au contexte économique, ceux liés à l’approvisionnement des
entreprises œuvrant dans le domaine des feuillus durs pourraient aussi être responsables de
la diminution de la récolte du bois. Depuis plusieurs années déjà, l’industrie des feuillus durs
fait face à la rareté des sciages de qualité supérieure des bois traditionnellement utilisés,
comme l’érable à sucre et le bouleau jaune (CRIQ 2002; MRNFPQ et CRIQ 2003; MRNFQ
et CRIQ 2007, 2008). À la fin des années 1980, les coupes à diamètre limite, qui ont eu pour
effet de dégrader le massif forestier et de réduire la qualité des bois sur pied (Metzger et
Tubbs 1971; Robitaille et Roberge 1981; Nyland 1992; Bédard et Majcen 2001; Bureau du
Forestier en chef 2012), ont été remplacées par les coupes de jardinage. En permettant de
régénérer et d'éduquer le peuplement tout en récoltant un certain volume de bois, la coupe de
jardinage vise à maintenir, voire améliorer, la productivité des forêts feuillues en prélevant
les arbres en perdition qui mourront avant la prochaine intervention (Arbogast 1957; Majcen
et al. 1990; Nyland 1998). Par conséquent, les taux d’accroissement et de survie, ainsi que la
qualité des arbres du peuplement résiduel dépendent de la stratégie de sélection des tiges
destinées à la récolte. Pour cette raison, il importe de pouvoir relier l’évaluation visuelle des
arbres effectuée lors des inventaires forestiers à la répartition du volume de bois par type
2
d’usine et à la qualité des produits transformés. Cette tâche est toutefois complexifiée par la
difficulté de relier l’apparence externe d’un arbre à la qualité interne de son bois.
Chez l’érable à sucre et le bouleau jaune, l’apparence visuelle du bois est une variable
déterminante de sa qualité puisqu’il sert surtout à la fabrication de meubles ou de parquets
(CRIQ 2002). La coloration de cœur est une des caractéristiques du bois de ces espèces qui
peut affecter leur qualité pour de tels usages. Elle fait référence à la modification uniforme
ou irrégulière de la couleur originale du bois d’une espèce donnée vers des teintes rougeâtres
ou brunâtres (Campbell et Davidson 1941; Shigo 1967). Techniquement, la coloration de
cœur est uniquement un critère visuel et esthétique n’affectant pas les propriétés mécaniques
de l’arbre (Shmulsky and Jones 2011). Par contre, dépendamment des tendances du marché,
des modes et des traditions, elle peut avoir un impact important sur la valeur du bois d’érable
à sucre et de bouleau jaune. Cette caractéristique est généralement considérée comme
indésirable puisqu’elle diminue la valeur des produits (Erickson et al. 1992; Hardwood
Market Report 2011).
Chez l’érable à sucre et le bouleau jaune, la coloration de cœur est d’origine traumatique
(Shigo 1966; Shigo 1967; Davidson et Lortie 1969; Shigo et Hillis 1973; Boulet 2007;
Belleville et al. 2011; Drouin et al. 2009), contrairement à certaines autres espèces pour
lesquelles un processus de coloration relié à la formation de duramen est en place. Chez les
deux espèces ciblées par ce projet, elle serait le résultat d’une série de processus liés aux
blessures, à l’oxydation des tissus et à l’action des microorganismes dans le bois (Shigo 1966;
Shigo 1967; Shigo et Larson 1969; Shigo et Hillis 1973; Solomon et Shigo 1976; Basham
1991). Les blessures, qu’elles soient causées par les branches mortes, les animaux ou
l’exploitation forestière, constitueraient une porte d’entrée potentielle pour la coloration en
exposant le bois du tronc aux conditions atmosphériques externes. Cette hypothèse est
appuyée par des études récentes qui ont établi des liens étroits entre les défauts externes
(nombre de branches mortes, nœuds, blessures et fourches) et la présence de coloration du
cœur (Knoke 2003; Wernsdorfer et al. 2005; Belleville et al. 2011). La réaction initiale d’un
arbre à la suite d’une blessure serait seulement liée à des processus chimiques impliquant,
d’une part, la production des composés phénoliques et, d’autre part, l’oxydation du bois
causée par l’entrée d’air dans l’arbre. Par la suite, les bactéries et les champignons non-
3
hyménomycètes peuvent infecter la blessure et amplifier le processus de coloration
(Campbell et Davidson 1941; Shigo 1966; Shigo et Hillis 1973; Sorz et Hietz 2008). Dans
certains cas, la coloration de cœur peut être suivie par un envahissement des champignons
hyménomycètes qui causent une dégradation du bois (Shigo 1966; Shigo 1967; Shigo et
Hillis 1973; Basham 1991).
Les études menées depuis une quarantaine d’années sur les feuillus durs de l’est de
l’Amérique du Nord et en Europe ont permis de mieux comprendre le développement de la
coloration de cœur à l’échelle de l’arbre. La coloration est influencée par l’âge, la sévérité et
la taille de la blessure (Shigo 1966), ainsi que par le diamètre, la hauteur et l’âge des arbres
(Campbell et Davidson 1941; Knoke 2003; Wernsdorfer et al. 2006; Giroud et al. 2008;
Drouin et al. 2009). La vigueur des arbres semble aussi jouer un rôle déterminant (Shigo et
Hillis 1973; Drouin et al. 2009; Baral et al. 2013). La coloration du bois est un processus lent
dont le développement prend des semaines (Sorz et Hietz 2008). Le bois qui est formé à la
suite d’une blessure ne sera généralement pas coloré, la coloration se limitant plutôt aux tissus
formés avant la blessure et se propageant vers l’intérieur de l’arbre (Solomon et Shigo 1976;
Basham 1991). Le développement de la coloration est plus rapide selon l’axe longitudinal
que l’axe radial de la tige, ce qui crée typiquement une colonne de coloration dans le tronc
(Campbell et Davidson 1941; Shigo et Larson 1969). Elle suit rarement une disposition
uniforme dans la tige, étant donné qu’elle est produite par la fusion de plusieurs colonnes de
coloration créées à des moments différents et selon diverses proportions (Campbell et
Davidson 1941; Shigo 1966). Toutefois, des études récentes ont permis de montrer que le
diamètre de la zone colorée diminue en montant dans l’arbre et prend un aspect généralement
fusiforme (Hallaksela et Niemisto 1998; Wernsdorfer et al. 2006; Giroud et al. 2008;
Belleville et al. 2011).
Malgré les nombreuses avancées dans la compréhension des facteurs affectant le
développement de la coloration à l’échelle de l’arbre, nous sommes toujours confrontés aux
incertitudes face aux facteurs qui influencent sa présence à une échelle plus vaste. Bien
qu’elle ait un impact majeur sur la qualité des approvisionnements, la distribution de la
coloration chez l’érable à sucre et le bouleau jaune entre les différentes régions du Québec
demeure peu documentée. Nous ne sommes donc pas en mesure de déterminer si le processus
4
de coloration de cœur peut être lié à des facteurs caractérisant les échelles du peuplement ou
de la région. Pourtant, des éléments nous font penser que l’influence du milieu et des
conditions de croissance pourraient effectivement avoir un effet important sur son
développement. En effet, plusieurs intervenants du milieu forestier prétendent que la
coloration de cœur chez l’érable à sucre et le bouleau jaune varie selon la provenance des
bois. Certains documents en font vaguement mention (Davidson et Lortie 1969; Boulet 2007;
Wiedenbeck et al. 2004), même si l’effet régional de la coloration n’a pas été observé chez
l’érable à sucre (Yanai et al. 2009). Quelques rares études (Climent et al. 2002) ont aussi
montré que le climat et le milieu de croissance pouvaient influencer le développement de la
coloration chez les espèces où un vrai processus de formation du duramen était en place.
Cependant, à notre connaissance, aucune étude précise n’a permis de démystifier le rôle joué
par le milieu de croissance dans la coloration de cœur de l’érable à sucre et du bouleau jaune.
En plus du manque de connaissances sur la distribution de la coloration de cœur des
principales espèces feuillues au Québec, l’industrie forestière fait aussi face aux incertitudes
liées à l’approvisionnement en bois feuillu qui découlent directement du système actuel de
marquage de tiges pour la récolte. Même si plusieurs variantes de la coupe de jardinage ont
vu le jour depuis son instauration en 1987, le mode de récolte est principalement axé vers le
jardinage par pied d’arbre ou par petit groupe d’arbres (Majcen et Richard 1992; Bédard et
Majcen 2001). Cette façon de faire vise à imiter le régime de perturbations naturelles des
forêts feuillues du Nord-Est de l’Amérique du Nord, produisant surtout une mortalité à
l’échelle de l’arbre ou du groupe d’arbres (Lorimer et Frelich 1994; Seymour et al. 2002).
Ainsi, depuis l’utilisation de normes de marquage associées au jardinage et aux autres types
de coupe partielle, les industries s’approvisionnant sur terres publiques n’ont pas accès à
l’ensemble des arbres d’un peuplement. Ces règles, jumelées à l’état des peuplements,
déterminent donc la qualité des approvisionnements pour les différents produits de
transformation envisagés (déroulage, sciage, pâte). Ainsi, même si un volume de bois est
alloué à une usine, son approvisionnement n’est pas assuré puisque la qualité des bois
marqués peut ne pas correspondre aux besoins réels de cette usine. Pour assurer
l’approvisionnement des usines de transformation de bois feuillu, le défi ne consiste donc
pas seulement à garantir un volume de bois récoltable, mais bien à déterminer un volume
correspondant à la qualité nécessaire à leur production rentable. Pour ce faire, on doit être en
5
mesure de relier le classement visuel des arbres sur pied effectué lors des inventaires
forestiers et la répartition du volume de bois par type d’usine et, idéalement, par classe de
qualité de produits transformés.
Depuis l’instauration des coupes de jardinage, le système de classement visuel utilisé pour
sélectionner les arbres destinés à la récolte a subi de nombreux changements. Jusqu’au milieu
des années 2000, c’est un système de marquage hybride (I-II-III-IV), tenant compte de la
vigueur et de la qualité des arbres, qui fût appliqué (Majcen et al. 1990). Le jardinage basé
sur le marquage de tiges selon ce système a fait ses preuves à l’échelle expérimentale (Majcen
et Richard 1992; Majcen 1996; Bédard et Majcen 2001; Coulombe et al. 2004; Majcen et al.
2006). Par contre, son application à l’échelle industrielle n’a pas permis d’atteindre les
objectifs visés. Coulombe et al. (2004) ont souligné que les pratiques de marquage de
l’industrie de transformation étaient non conformes aux principes de la coupe de jardinage
visant à améliorer la productivité des forêts et à augmenter la production en bois d’œuvre de
feuillus durs. Dans leur suivi des effets réels des coupes de jardinage dans les forêts publiques
du Québec de 1995 à 1998, Bédard et Brassard (2002) ont mis en évidence le fait que
l’accroissement net des peuplements jardinés dans les dispositifs de recherche du Ministère
des Forêts, de la Faune et des Parcs du Québec (MFFPQ) était plus de deux fois supérieur à
celui enregistré dans les peuplements jardinés dans le cours normal des opérations des
entreprises forestières. Ces difficultés d’application à l’échelle industrielle ont été associées
au choix inadéquat des arbres à prélever. Selon plusieurs intervenants, le système de sélection
de Majcen et al. (1990) laissait trop de latitude et d’interprétation aux marteleurs. Face à cette
problématique et aux recommandations de la Commission d'étude sur la gestion de la forêt
publique québécoise (Coulombe et al. 2004), le MFFPQ a raffiné le système de classification
des arbres feuillus du Québec.
La nouvelle classification est issue d’un système basé sur des connaissances pathologiques
appliquées surtout pour déterminer la vigueur des arbres (Boulet 2007). Quatre priorités de
récolte (M-S-C-R) guident l’ordre de sélection des tiges en fonction de défauts
pathologiques, morphologiques ou mécaniques précis. Ces défauts sont reliés à une
évaluation de la probabilité de mortalité d’un arbre avant la prochaine rotation (Boulet 2007).
La classification priorise la récolte des arbres mourants et dont la survie semble être
6
compromise (classes M et S). Ainsi, ce système vise la restauration des forêts feuillues, mais
il ne considère pas directement les variables déterminant la qualité des arbres. Fortin et al.
(2009b) ont déterminé que la capacité du système de classification MSCR à établir la
répartition du volume des arbres par classe de qualité est globalement faible.
Conséquemment, l’instauration de ce système est venue exacerber le problème
d’approvisionnement décrit plus haut. La situation pourrait être améliorée en jumelant des
classes de qualité au système MSCR (Fortin et al. 2009b). Des efforts ont été consentis en ce
sens avec l’intégration de classes de qualité additionnelles (classes O et P) (MRNFQ 2006),
mais le gain en précision apportée par ces nouvelles classes n’a jamais été quantifié. Dans
une perspective d’amélioration des prévisions d’approvisionnements, l’apport de nouvelles
variables prédictives, à l’échelle de l’arbre et du peuplement, devrait aussi être évalué.
Afin d’atteindre le plein potentiel de mise en valeur des forêts feuillues, le système de
marquage doit permettre l’atteinte de l’objectif sylvicole, par le prélèvement des arbres
dépérissants, mais aussi celui d’approvisionnement qui affecte la viabilité des usines de
transformation. Une part des éléments déterminant la qualité du bois des feuillus durs est
reliée à des facteurs morphologiques facilement évaluables par des systèmes de classification
visuelle. D’autres facteurs, comme la coloration de cœur, sont reliés à des facteurs internes.
Il importe, dans un premier temps, de mieux comprendre les facteurs faisant varier la qualité
des approvisionnements et, dans un second temps, d’inclure ces derniers dans nos systèmes
guidant la sélection des tiges.
Démarche méthodologique
L’objectif général de ce projet de recherche était d’améliorer les prévisions
d’approvisionnement des usines de transformation de bois feuillu à partir d’une meilleure
évaluation de la qualité des arbres feuillus sur pied. L’approche proposée par cette étude vise
à préciser la répartition géographique de la coloration de cœur tout en établissant des liens
étroits entre l’évaluation visuelle des arbres sur pied, leur vigueur et la valeur des produits
transformés en usine. L’ensemble du projet de recherche porte sur l’étude de deux principales
espèces feuillues du Québec, l’érable à sucre et le bouleau jaune.
7
Le premier chapitre de la thèse porte sur la distribution régionale de la coloration de cœur de
l’érable à sucre et du bouleau jaune. Douze localisations couvrant l'ensemble de la forêt
tempérée du sud du Québec ont été échantillonnées afin de quantifier la variation de la
proportion de la coloration de cœur à l’échelle de la province.
L’objectif du second chapitre était d’améliorer les directives de martelage, présentement
axées uniquement sur la vigueur, en déterminant les principales variables qui affectent la
valeur monétaire de l’érable à sucre et du bouleau jaune sur pied. Afin d’identifier les arbres
moribonds pouvant produire au moins une bille de sciage, un mesurage détaillé, incluant une
caractérisation de tous les défauts externes, a été effectué sur 96 arbres répartis dans deux
stations. Ce même échantillonnage a également servi à réaliser le troisième volet de cette
thèse.
Le troisième chapitre de la thèse vise à décrire le lien entre les caractéristiques des billes
destinées au sciage et les planches produites. Plus précisément, le but de ce volet était de bâtir
un modèle de prévision de l’occurrence et du volume des grades et des catégories de couleur
des planches sciées en fonction des caractéristiques des billes d’érable à sucre et de bouleau
jaune. Les résultats de ce volet permettent de caractériser le panier de produits découlant du
sciage et peuvent servir à établir la valeur monétaire des bois.
Afin de prendre en considération les principales variables liées à la valeur des arbres feuillus
sur pied, les aspects de qualité de l’érable à sucre et du bouleau jaune, traités dans cette thèse,
sont abordés à deux échelles. Le premier volet aborde la distribution de la coloration de cœur
à l’échelle régionale. Les chapitres deux et trois, pour leur part, sont axés sur une évaluation
visuelle aux échelles des arbres et des billes, en établissant des liens étroits avec la valeur et
la qualité des produits transformés en usine. Le dernier chapitre permet également de faire le
lien avec les deux premiers volets de la thèse, en caractérisant l’effet de la coloration de cœur
sur le panier de produits et, ultimement, sur la valeur monétaire des arbres. Ainsi, les
ajustements proposés fourniront un outil d’aide à la décision au MFFPQ lui permettant
d’attribuer, avec plus de précision, des volumes de bois aux différents types d’usines de
transformation (déroulage, sciage, pâte). De plus, ces résultats permettront de mieux
caractériser les peuplements forestiers lors de l’éventuelle vente aux enchères de leur bois.
9
Chapitre 1
Regional variation in the proportion of red heartwood in
sugar maple and yellow birch1
1 Version intégrale d’un article publié / Intergral version of a published paper:
Havreljuk, F., Achim, A. and Pothier, D. 2013. Regional variation in the proportion of red heartwood in sugar
maple and yellow birch. Can. J. For. Res. 43(3), 278–287. doi:10.1139/cjfr-2012-0479
10
Abstract
Stems of sugar maple (Acer saccharum Marsh.) and yellow birch (Betula alleghaniensis
Britt.) trees often contain a column of discoloured wood known as red heartwood, which
reduces lumber value. To quantify the regional-scale variation in red heartwood, 192 trees of
each species were sampled in 12 locations across the temperate forest zone of southern
Québec, Canada. Large regional variation in the radial proportion of red heartwood (RHP) at
breast height (1.3 m) was observed in both species. Statistical modeling showed that such
variation was mainly attributable to factors related to tree development. Cambial age had a
strong positive effect on RHP in both species, suggesting that the occurrence of red
heartwood ultimately might be unavoidable. There was also a positive effect of ring area
increment at the limit of the discoloured zone. In the case of sugar maple, there was an added
effect of the trend in ring area increments observed in the same zone, with a negative trend
being generally indicative of a larger RHP. Further variability in this species was also
associated with the annual minimum temperature of the sampling locations. The models
developed for each species explained around 60% of the variance in RHP and could be used
to improve forest management and wood procurement decisions.
Keywords: sugar maple, yellow birch, red heartwood, wood discoloration, appearance wood
products, regional climate.
11
Résumé
Les tiges d'érable à sucre (Acer saccharum Marsh.) et de bouleau jaune (Betula
alleghaniensis Britt.) contiennent fréquemment une colonne de bois brun-rougeâtre, appelée
coloration de cœur, qui réduit la valeur des produits du bois. Afin d'en quantifier la variation
à l'échelle régionale, 192 arbres de chaque espèce ont été échantillonnés dans 12 localisations
couvrant l'ensemble de la forêt tempérée du sud du Québec, Canada. Une variation régionale
élevée de la proportion radiale de la zone colorée (PRC) à hauteur de poitrine (1,3 m) a été
observée chez les deux espèces. La modélisation statistique a révélé que cette variation était
principalement attribuable à des facteurs liés au développement des arbres. L'âge cambial
avait un effet positif sur la PRC des deux espèces, ce qui indique que l'occurrence de la
coloration de cœur serait ultimement inévitable. Un effet positif de la superficie des anneaux
de croissance à la limite de la zone colorée a aussi été observé. Dans le cas de l'érable à sucre,
il y avait un effet additionnel de la tendance de l’accroissement en superficie des anneaux
dans la même zone, les tendances négatives étant généralement indicatrices d'une PRC plus
élevée. Une partie de la variabilité chez cette espèce était aussi associée à la température
minimale annuelle d'une localisation. Les modèles mis au point pour chaque espèce
expliquent près de 60 % de la variance et pourront être utilisés pour améliorer les décisions
liées à l'aménagement forestier et aux approvisionnements en bois.
Mots-clés : érable à sucre, bouleau jaune, cœur rouge, coloration du bois, produits
d’apparence, climat régional.
12
Introduction
Sugar maple (Acer saccharum Marsh.) and yellow birch (Betula alleghaniensis Britt.) are
dominant components of the North American temperate deciduous forests. Both tree species
are commercially important, especially as raw material for appearance wood products such
as furniture, flooring, cabinets, and interior finishing (CRIQ 2002). Accordingly, the wood
quality and market value of sugar maple and yellow birch depend on the visual characteristics
of sawn boards.
Red heartwood is one of the most important appearance criteria for such products. Also
referred to as red heart, heartwood discolouration, staining heart, traumatic heartwood, false
heartwood, pathological heartwood, and, mistakenly, as mineral stain, it consists of a uniform
or irregular change of the original wood colour to a darker reddish-brown colour (Campbell
and Davidson 1941; Shigo 1966, 1967; Hillis 1987; Basham 1991; Erickson et al. 1992;
Hallaksela and Niemisto 1998; Drouin et al. 2009). Although the presence of uniform red
heartwood is desirable for some end-uses, the simultaneous presence of light-coloured
sapwood and red heartwood is generally considered unappealing by consumers. As a result,
heartwood discolouration significantly reduces lumber value (Erickson et al. 1992;
Hardwood Market Report 2011).
Whereas coloured heartwood in some other species, like oak and cherry, is part of a normal
aging process (Hillis 1987), heartwood discolouration in sugar maple and yellow birch is
believed to originate from trauma (Shigo 1966; Davidson and Lortie 1969; Shigo and Hillis
1973). Injuries to the stem may induce wood oxidation and microbial activity, which can
result in discolouration (Shigo 1967; Solomon and Shigo 1976). Red heartwood does not
affect wood mechanical properties (Shmulsky and Jones 2011), but could be followed by an
invasion of hymenomycete fungi that cause wood decay (Basham 1991).
To date, research has focused on the development and within-tree distribution of red
heartwood. Some studies have found a relationship between the proportion of red heartwood
and tree diameter, height, and age (Campbell and Davidson 1941; Knoke 2003; Wernsdorfer
et al. 2006; Giroud et al. 2008; Drouin et al. 2009). It can also be related to the severity and
13
size of bole injuries induced by logging (Shigo 1966), further supporting the trauma
hypothesis. Recent studies on European beech (Fagus sylvatica L.) and paper birch (Betula
papyrifera Marsh.) provided more evidence by demonstrating direct relationships between
external defects (e.g., number of dead branches, knots, injuries, and forks) and the occurrence
and extent of red heartwood (Knoke 2003; Wernsdorfer et al. 2005; Belleville et al. 2011).
Little scientific attention has been paid to the factors that may explain regional-scale
variation, despite the potential benefits that might accrue to members of the wood products
supply chain, where these variations are understood. Some stand-level variation in red
heartwood occurrence has been reported for several hardwood species (Davidson and Lortie
1969; Wiedenbeck et al. 2004). Soil fertility might be responsible for site-to-site differences,
although this was not found to be the case in a study conducted in the northern United States
(Yanai et al. 2009). Regional differences might also be attributable to variation in radial
growth rate, which is related to the size of defects and the time to wound closure (Solomon
and Blum 1977; Vasiliauskas 2001). Alternatively, regional differences in red heartwood
development might originate from climatic factors, which are known to regulate tree growth
and physiological processes (Pither 2003; Klos et al. 2009). Some observations suggest that
the proportion of red heartwood generally increases in colder climates (Wiedenbeck et al.
2004). This could be related to the increased occurrence of external stem defects towards the
northern limit of the sugar maple distribution range (Burton et al. 2008). For example, defects
such as frost cracks are frequently accompanied by discoloured and decayed wood (Shigo
1966, 1967; Davidson and Lortie 1969).
The reasons for initiating this study were first to describe the variation in red heartwood
proportion at a regional scale and second to attempt to explain the observed differences. Our
underlying hypothesis was that, if regional variation in red heartwood proportion actually
exists, it can be explained by differences in tree age and radial growth rate alone. Rejection
of this hypothesis would imply an additional influence of other factors, such as stand-level
variables (e.g., basal area, number of stems per hectare, etc.). Red heartwood was found to
propagate longitudinally along the annual rings forming a column of discoloured wood
(Hallaksela and Niemisto 1998; Wernsdorfer et al. 2005; Giroud et al. 2008). The diameter
of the heartwood zone has also been positively related to the number and size of dead branch
14
scars (Solomon and Shigo 1976; Belleville et al. 2011), which are factors closely related to
tree age and radial growth rate.
Materials and methods
Study sites and field measurements
Twelve sampling regions were selected across the temperate forest zone of southern Québec,
Canada (Figure 1.1). The sites were all located on public land, within the sugar maple –
yellow birch or the balsam fir (Abies balsamea [L.] Mill.) – yellow birch bioclimatic domains
(Saucier et al. 1998) (Table 1.1).
Figure 1.1 Location of the sampling regions across Québec.
15
Table 1.1 Summary of sampling locations used in the study.
Region
ID Name Bioclimatic domain
Bioclimatic
subdomain
Ecological
region
Elevation
range (m)
1 Témiscamingue Sugar maple – yellow birch West 3a 325-385
2 Rapides-des-Joachims Sugar maple – yellow birch West 3a 245-315
3 Réservoir Cabonga Balsam fir– yellow birch West 4b 395-405
4 Outaouais Sugar maple – yellow birch West 3b 325-410
5 Ste-Véronique Sugar maple – yellow birch West 3b 345-370
6 Mauricie Sugar maple – yellow birch East 3c 275-345
7 Portneuf Balsam fir– yellow birch West 4c 375-495
8 Duchesnay Balsam fir– yellow birch East 4d 225-295
9 Lac Mégantic Sugar maple – yellow birch East 3d 545-590
10 Montmagny Sugar maple – yellow birch East 3d 360-380
11 Charlevoix Balsam fir– yellow birch East 4d 295-345
12 Squatec Balsam fir– yellow birch East 4f 365-415
We restricted the choice to uneven-aged stands with a main canopy dominated by mature
sugar maple and (or) yellow birch trees established on glacial tills deeper than 50 cm, and
characterized by mesic conditions (average fertility and drainage). Recently harvested sites
(<10 years) and those with severe past biotic and abiotic disturbances were rejected from the
sampling. Once these criteria were defined, we collaborated with local authorities to create a
bank of potential sampling sites in each region using forest cover maps. A random list of
potential sites was then generated and these were either rejected or retained based on field
validations of the criteria, until two study sites were selected for each species in each region.
Sampling of both species was possible at eight sites that met the selection criteria. Stand
structure and composition were measured using variable-radius plots. Two plots were
established for sampling sites covering less than one hectare and one additional plot was
established for each additional hectare.
To minimize variability between trees and focus on regional variation, the sampling was
limited to trees with a diameter between 23.1 and 33.0 cm at breast height (DBH, 1.3 m above
the ground). This range corresponds to the small sawlog timber category of the hardwood
tree grading system (Hanks 1976; Monger 1991). To limit the variability associated with
factors other than regional climate, site properties, and tree growth, only vigorous trees were
selected using the tree-marking criteria of Boulet (2007). To facilitate the sampling of
undamaged cores, trees with pathogens and severe wounds were avoided, since these are
16
often associated with stem decay. Trees were also rejected if they had an abnormal number
of dead branches or other obvious external initiation points for red heartwood (Belleville et
al. 2011) on the lower 5 m of the stem. The sampling was also limited to trees with a dominant
and codominant position in the main canopy. Following these criteria, eight sample trees per
species per site were randomly selected for sampling.
On each sample tree, DBH and total tree height were recorded (Table 1.2) and then an
increment core sample was taken at breast height. To control for any potential effects of trees
growing on an incline, cores were consistently sampled from the uphill side of each tree. The
core samples provided an assessment of red heartwood and radial growth rate in the butt log,
which is the most valuable part of the tree (Fortin et al. 2009b). In addition, maximum
heartwood area is located around breast height (Hillis 1987; Giroud et al. 2008).
Table 1.2 Mean sample tree characteristics. SD is the standard deviation.
Sugar maple Yellow birch
Variable Mean ± SD Range Mean ± SD Range
Dbh (cm) 28.3 ± 2.8 23.1 – 33.0 28.0 ± 2.7 23.1 – 33.0
Height (m) 20.6 ± 2.2 15.1 – 26.1 19.7 ± 2.1 14.6 – 26.4
Age (years) 93 ± 22 57 – 155 83 ± 23 31 – 153
Sample core processing
All cores were air-dried and progressively sanded down to allow a clear identification of
growth rings. A total of 192 sugar maple and 192 yellow birch cores were processed and
scanned at high resolution using an optical scanner (Epson GT-15000, Japan).
The distinction between discoloured heartwood and light-coloured wood was in most cases
abrupt but was harder to detect in some samples owing to a gradual transition. To avoid
subjectivity, the limit between discoloured and noncoloured wood was determined in a two-
step method using the image-processing software ImageJ (Abramoff et al. 2004). First, a
threshold function was executed to divide the scanned image into either features of interest
(i.e., red heartwood and sapwood) or background. An iterative threshold selection procedure
was applied (Ridler and Calvard 1978). In the second step, the noise generated by the
17
threshold method was removed to obtain a clear boundary between red heartwood and
sapwood area (Figure 1.2).
Figure 1.2 Illustration of the red heartwood separation procedure performed using ImageJ.
(A) Initial image. (B) The resulting image after applying the threshold function. (C) The final
image after the noise from the threshold function was removed.
All samples were processed individually using the same procedure. They were calibrated and
corrected for any artifacts and (or) breakages, to ensure that accurate lengths were used in
subsequent analyses. Some samples were soaked in water to improve the contrast between
the discoloured and noncoloured wood. The total radial core length (from pith to bark) and
the length of discoloured wood were measured on each sample.
Tree-ring increments were measured using the semiautomatic image analysis system
WinDendro (Guay et al. 1992). To ensure accuracy, samples were first analyzed under a
magnifying glass and the less discernible rings were marked with a pencil. Annual ring width
increments were converted into ring area increments using the method described by LeBlanc
(1996). Following previous studies (Shigo 1966, Hallaksela and Niemisto 1998; Wernsdorfer
et al. 2005), red heartwood was assumed to be symmetrically distributed around the pith, and,
therefore, the radial measurements on each core were converted into area values that assumed
circularity of the stems.
Climatic characterization
The climatic data used in our analyses were generated by BioSIM (Régnière et al. 2012).
This software computes annual climatic variables for a given site using the North American
Normals database (Canada–USA 1981–2010), which contains monthly statistics over the
most recent 30-year period before the trees were sampled. Geographic coordinates of latitude,
longitude, and elevation from all study sites were set as BioSIM inputs. The software was
parameterized to generate climate information using an interpolation between the eight
18
closest available weather stations. BioSIM is a simulator that generates a series of daily
values with a random component. Averages are reported along with their mathematical
expectation of average, variance, autocorrelation, and cross-correlation of minima and
maxima. All simulations were conducted in a single operation with 500 iterations to ensure
regular results. More than 20 climatic variables were generated using this method.
Statistical analysis
The dependent variable used in this study was the red heartwood proportion (RHP) at 1.3 m
in height, representing the ratio of the discoloured wood radius to the total radius of the core.
This choice was made to reflect the typical grade sawing of hardwoods (Steele 1984), which
consists of extracting noncoloured wood boards from the bark towards the pith until the
discoloured core is reached. The radial proportion of discoloured wood was preferred to the
cross-sectional area proportion as it was found to be normally distributed.
All statistical tests were performed using the R statistical programing software (R
Development Core Team 2012). Mixed linear models were developed for each species
separately using the nlme package. Region and site nested in region were considered as
random effects, in accordance with the sampling strategy (Gelman and Hill 2007). The initial
steps of the analysis aimed to describe the local and regional patterns of variation in red
heartwood. To assess the importance of different variables associated with RHP, models were
compared using the corrected Akaike information criterion (AICc) (Burnham and Anderson
2002). This statistic was used to guide model development by balancing the fit (i.e., log-
likelihood) and parsimony (i.e., number of parameters) of each model. To avoid over-fitting
and reporting spurious effects, a limited set of candidate models were used to test biologically
plausible hypotheses (Burnham and Anderson 2002; Anderson 2008).
Model development
Twenty a priori multilevel linear models were developed and compared to identify the main
factors related to RHP in sugar maple and yellow birch. The first group of candidate models
included individual tree descriptors such as tree height and age (i.e., cambial age at 1.3 m),
19
which are known to be associated with red heartwood size in other hardwood species
(Wernsdorfer et al. 2006; Giroud et al. 2008).
A second group of candidate models was created to describe tree development. The
explanatory variables “growth rate”, or periodic annual increment, and “growth trend”,
representing the rate of change in mean annual growth within a given time period (Bigler and
Bugmann 2003), were derived from annual ring increments. Such variables have been used
successfully in mortality models because of their link with tree vigor (Bigler and Bugmann
2003; Hartmann et al. 2008). Both variables were represented using ring area increments
(RAI, cm2/year), which are recognized as a more meaningful indicator of tree growth and
vigor than ring width (LeBlanc 1996). Five year growth rate was measured on each sample
in a period that ended at the discoloured wood boundary (RAIBC5). This variable was deemed
to be representative of the size of the live crown (Valentine and Mäkelä 2005) and hence the
number and size of live branches at the time when the ring at the edge of the discoloured
zone was formed. Likewise, the slope of a local linear regression applied to ring area over a
period of 10 years spanning the current boundary between discoloured and noncoloured
wood (i.e., five rings on each side) (SLR10) was used as a potential explanatory variable. This
was deemed to represent the growth trend at the time when the ring at the limit of the
discoloured zone was formed. If RAIBC5 can be considered as an indicator of the number and
size of the live branches present at that time, SLR10 could be indicative of further growth
prior to branch death. A 10 year time interval was chosen in this case to increase the number
of points in the regression and limit the influence of unusually large or narrow rings on the
obtained value. Average annual tree increment (AAI) over the whole pith-to-bark profile was
used as a long-term measure of tree vigor. Because this variable was not normally distributed,
a logarithmic transformation was applied prior to model fitting.
The third set of candidate models included the basal area of the stand (StandBA, m2/ha). It
was hypothesized that RHP would be positively correlated with basal area because increased
competition for light may lead to faster crown recession and, therefore, to increased branch
mortality (Shmulsky and Jones 2011).
20
Climatic variables were then added to the fourth group of candidate models. Only a limited
number of climatic variables generated by BioSIM and those relevant to our hypotheses were
chosen based on preliminary analyses and data exploration. Explanatory variables related to
temperature (annual means and extremes) and precipitation (annual sums) were included in
the final set of candidate models.
Finally, an intercept-only model was added to ensure it did not perform better than more
complex models. A summary of all candidate variables is presented in Table 1.3.
Table 1.3 List of explanatory variables screened in the modeling process.
Variable Description
Age (years) Cambial age at 1.3 m
Height (m) Height of the tree
AAI (cm2/year) Log-transformed mean ring area increment
RAIBC5 (cm2/year) 5-year mean ring area increment at the limit of the red heartwood zone
SLR10 Linear regression slope of ring area values over 10 years spanning the limit of the red
heartwood zone (i.e., 5 rings on each side)
StandBA (m2/ha) Stand basal area
LTMin (°C) Annual lowest daily minimum temperature
MTMean (°C) Annual mean daily average temperature
Precip (mm) Annual total precipitation
Autocorrelation between variables was checked during the model construction process using
a variance inflation factor (VIF) (Zuur et al. 2010). The usual assumptions for regression
analysis were checked and no problems were detected. All selected models presented
normally distributed errors, homogeneous variances and no extreme values. For the
simplification of interpretation and to limit the number of candidate models, only additive
effects were considered (i.e., no interactions). Before model comparison, four sugar maple
and five yellow birch trees were rejected from the analyses because of missing discoloured
heartwood and thus RAIBC5 and SLR10 data. Model selection was performed using the
AICcmodavg package in R (Mazerolle 2012). This allowed uncertainties regarding the
selection of the best model to be assessed using a model averaging technique (also referred
to as “multimodel inference”). The package computes the weighted estimates of the
predictions for a given predictor variable across all models. The weighting of parameter
estimates is given by the model probabilities, which are derived from Akaike's weights. For
21
a detailed description of this approach see Burnham and Anderson (2002) or Mazerolle
(2006).
Results
Of the 192 samples per species, only four sugar maple and five yellow birch cores did not
contain discoloured heartwood. The mean radial proportions (±SD) of red heartwood were
36.4 ± 14.9% and 36.8 ± 15.5% for sugar maple and yellow birch, respectively. Important
variations of RHP were observed between the sampling regions (Figure 1.3).
Figure 1.3 Mean red heartwood proportion (RHP) for sugar maple and yellow birch in the 12
sampling regions. Two study sites are included in each region and eight trees were sampled
from each site. Error bars represent standard errors.
There were no differences in RHP between bioclimatic domains, but significant differences
(p < 0.05) were detected between subdomains. In sugar maple, mean RHP was approximately
44% in the western bioclimatic subdomains, compared with 29% in the eastern subdomains.
However, no such trend was observed for yellow birch (Figure 1.4).
22
Figure 1.4 Mean red heartwood proportion (RHP) for sugar maple and yellow birch across
bioclimatic subdomains. Eastern Balsam fir – Yellow birch subdomain (n = 92), Western
Balsam fir – Yellow birch subdomain (n = 64), Eastern Sugar maple – Yellow birch
subdomain (n = 92), and Western Sugar maple – Yellow birch subdomain (n = 128). Error
bars represent standard errors.
The mean age of trees sampled in the western subdomains was greater (97 and 86 years for
sugar maple and yellow birch, respectively) than in their eastern counterparts (88 and 78
years for sugar maple and yellow birch, respectively). Annual ring measurements on the
sample cores revealed that (i) age varied substantially between the samples despite the limited
range of DBH and (ii) RHP was strongly related to age for both species (Figure 1.5).
23
Figure 1.5 Number of discoloured wood rings as a function of the total number of rings at
1.3 m.
The best model for predicting RHP in sugar maple was model 13 (AICc = 1335.06, wi =
0.75), which included tree, growth, and climate variables, followed by model 17 with a
difference in AICc of 3.72 units (Table 1.4). The uncertainty regarding the best model (model
13) was assessed using model averaging. According to the 95% confidence intervals (CI) for
the model-averaged regression estimates, RAIBC5 (CI = 2.25–3.08), SLR10 (CI = −7.89 to
−0.66), Age (CI = 0.11–0.23), and LTMin (CI = −2.12 to −0.57) all showed strong evidence
of having a significant influence (effect ≠ 0 with p < 0.05) on RHP (Figure 1.6). However,
there was insufficient evidence for Height (CI = −0.87 to 0.34) and StandBA (CI = −0.38 to
0.35) to be included in model 17. The adjusted R2 of model 13 was 0.67, but this decreased
to 0.60 when calculated from the fixed effects only. Parameter estimates are presented in
Table 1.5.
24
Table 1.4 Comparison of the multiple linear regression models for sugar maple red heartwood
proportion (RHP).
Model group Explanatory variables ID Log-
likelihood K AICc ∆i wi
Intercept only Null 1 -725.98 4 1460.17 125.11 0.00
Tree Age 2 -720.12 5 1450.56 115.50 0.00
Age + Height 3 -719.99 6 1452.44 117.38 0.00
Tree + Growth AAI 4 -724.82 5 1459.98 124.92 0.00
RAIBC5 5 -684.32 5 1378.96 43.90 0.00
RAIBC5 + SLR10 6 -680.47 6 1373.41 38.35 0.00
Age + Height + RAIBC5 7 -665.12 7 1344.87 9.81 0.01
Age + Height + RAIBC5 + SLR10 8 -662.43 8 1341.66 6.60 0.03
Age + RAIBC5 + SLR10 9 -662.80 7 1340.21 5.15 0.06
AAI + Height 10 -723.85 6 1460.17 125.11 0.00
Tree + Growth +
Stand Age + Height + RAIBC5 + SLR10 + StandBA 11 -662.42 9 1343.86 8.80 0.01
AAI + Height + StandBA 12 -723.58 7 1461.78 126.72 0.00
Tree + Growth +
Climate Age + RAIBC5 + SLR10 + LTMin 13 -659.13 8 1335.06 0.00 0.75
AAI + LTMin 14 -720.17 6 1452.79 117.73 0.00
Age + RAIBC5 + SLR10 + Precip 15 -662.39 8 1341.58 6.52 0.03
AAI + Precip 16 -723.91 6 1460.28 125.22 0.00
Full model Age + Height + RAIBC5 + SLR10 + StandBA + LTMin 17 -658.77 10 1338.78 3.72 0.12
AAI + Height + StandBA + LTMin 18 -719.26 8 1455.33 120.27 0.00
Age + Height + RAIBC5 + SLR10 + StandBA + Precip 19 -662.01 10 1345.26 10.20 0.00
AAI + Height + StandBA + Precip 20 -722.71 8 1462.22 127.16 0.00
Note: K is the total number of parameters (including an intercept and random terms), ∆i is the difference in
AICc with the best model, wi is the ratio of the ∆i for a given model to that of the whole set of candidate models.
A description of the abbreviations used is given in Table 1.3.
Figure 1.6 Model-averaged predictions and unconditional 95% confidence intervals for the
best-fit model parameters for sugar maple.
25
Table 1.5 Parameter estimates and their standard errors (±SE) for the final models.
Parameter Sugar maple Yellow birch
Intercept -40.14 ± 16.22 -18.43 ± 7.14
RAIBC5 2.66 ± 0.21 2.19 ± 0.17
SLR10 -4.29 ± 1.85 –
Age 0.17 ± 0.03 0.23 ± 0.03
Height – 1.30 ± 0.36
LTMin -1.32 ± 0.43 –
Note: A description of the abbreviations used is given in Table 1.3.
For yellow birch, the best model for predicting RHP was model 7 (AICc=1361.03; wi =0.52),
which included tree and growth variables, but several more complex models had very similar
AICc values (Table 1.6). There was sufficient empirical support for models 8 (∆i = 1.72; wi
= 0.22), 19 (∆i = 3.34; wi = 0.10), 17 (∆i = 3.66; wi = 0.08) and 11 (∆i = 3.92; wi = 0.07) as
the choice of the best model. Through model averaging, RAIBC5 (CI = 1.86−2.54), Age (CI
= 0.18−0.30) and Height (CI = 0.58−1.98) were confirmed to have a significant effect on
RHP (Figure 1.7). However, there was insufficient evidence for SLR10 (CI= −2.04 to 4.29),
StandBA (CI = −0.49 to 0.69), MTMean (CI = −0.47 to 4.92) and Precipitation (CI = 0−0.02)
to be included. The competing models all had the same basic structure as model 7, but
contained additional explanatory variables. Model averaging showed that the inclusion of
these additional covariates did not substantially improve the model fit. The adjusted R2 of
model 7 was 0.65, decreasing to 0.60 when calculated from the fixed effects only. Parameter
estimates are presented in Table 1.5.
26
Table 1.6 Comparison of the multiple linear regression models for yellow birch red
heartwood proportion (RHP).
Model group Explanatory variables ID Log-
likelihood K AICc ∆i wi
Intercept only Null 1 -752.04 4 1512.30 151.27 0.00 Tree Age 2 -743.01 5 1496.35 135.32 0.00
Age + Height 3 -731.76 6 1475.98 114.96 0.00 Tree + Growth AAI 4 -751.90 5 1514.13 153.10 0.00
RAIBC5 5 -702.67 5 1415.67 54.64 0.00
RAIBC5 + SLR10 6 -702.53 6 1417.52 56.49 0.00
Age + Height + RAIBC5 7 -673.20 7 1361.03 0.00 0.52
Age + Height + RAIBC5 + SLR10 8 -672.97 8 1362.74 1.72 0.22
Age + RAIBC5 + SLR10 9 -678.71 7 1372.05 11.03 0.00
AAI + Height 10 -740.87 6 1494.20 133.18 0.00 Tree + Growth +
Stand Age + Height + RAIBC5 + SLR10 + StandBA 11 -672.96 9 1364.94 3.92 0.07
AAI + Height + StandBA 12 -739.47 7 1493.57 132.54 0.00
Tree + Growth + Climate
Age + RAIBC5 + SLR10 + MTMean 13 -676.35 8 1369.51 8.49 0.01
AAI + MTMean 14 -751.25 6 1514.97 153.94 0.00
Age + RAIBC5 + SLR10 + Precip 15 -677.73 8 1372.26 11.24 0.00
AAI + Precip 16 -751.68 6 1515.83 154.80 0.00
Full model Age + Height + RAIBC5 + SLR10 + StandBA + MTMean 17 -671.72 10 1364.69 3.66 0.08
AAI + Height + StandBA + MTMean 18 -739.41 8 1495.63 134.60 0.00
Age + Height + RAIBC5 + SLR10 + StandBA + Precip 19 -671.56 10 1364.37 3.34 0.10
AAI + Height + StandBA + Precip 20 -738.81 8 1494.43 133.40 0.00
Note: K is the total number of parameters (including an intercept and random terms), ∆i is the difference in
AICc with the best model, wi is the ratio of the ∆i for a given model to that of the whole set of candidate models.
A description of the abbreviations used is given in Table 1.3.
Figure 1.7 Model-averaged predictions and unconditional 95% confidence intervals for the
best-fit model parameters for yellow birch.
Discussion
The results of this study confirm that there is regional variation in the proportion of
discoloured wood in both sugar maple and yellow birch. Our initial hypothesis was generally
supported for both species, since tree age and growth variables explained a large percentage
27
of the regional variation in RHP. Tree age was strongly related to the observed variation from
west to east, as older trees of both species were generally found in the western part of the
study area. The fact that discolouration is an age-dependent process (Figure 1.5) is consistent
with several observations made in other hardwoods (Campbell and Davidson 1941;
Hallaksela and Niemisto 1998; Knoke 2003; Giroud et al. 2008; Drouin et al. 2009; Belleville
et al. 2011). As proposed by Giroud et al. (2008), the effect of tree age on the discoloured
wood proportion may be explained by the accumulation of injuries over time and the normal
decrease in tree vigor. Indeed, branch mortality and the subsequent processes of branch
degradation, self-pruning, and wound healing continue over the lifespan of the tree. This
suggests that red heartwood formation is a traumatic but unavoidable process that occurs in
some hardwood species.
Several studies have identified dead branches as the main entry point for discolouration in
many hardwood species (Hallaksela and Niemisto 1998; Wernsdorfer et al. 2005; Belleville
et al. 2011). One possible explanation is that dead branch stubs create pathways for oxygen
and microorganisms (Shigo 1967; Sorz and Hietz 2008). Therefore, for a given tree age,
heartwood size could vary as a function of either the cumulative area of dead branches or of
the elapsed time until a wound heals. Our results for both species showed that larger red
hearts were associated with larger ring area at the limit of the discoloured wood column
(RAIBC5). This variable could be considered as an indicator of the number and (or) size of
the external defects, mainly in the form of knots, linked to the discolouration column. Indeed,
large ring widths at the edge of the discoloured wood boundary are indicative of previous
vigorous growth, which in turn is driven by a large live crown containing large and (or)
numerous branches. Based on the findings from tree dissection studies (Wernsdorfer et al.
2005; Giroud et al. 2008; Belleville et al. 2011), we can assume that most of the live branches
present when those rings were formed had died by the time our sampling was conducted.
Therefore, an early period of vigorous radial growth, followed by a period of crown
recession, would likely lead to a high proportion of red heartwood for a given tree age.
This would also explain the negative effect of the trend in ring area increments at each side
of the red heartwood boundary (SLR10) observed in the final model for sugar maple. In this
case, a negative slope of the local regression might be indicative of a slower healing process
28
(i.e., a longer time before branch occlusion), leading to an increase in RHP. As demonstrated
by Hein (2008) in European beech, a long period between branch death and occlusion can
lead to a greater proportion of heartwood. Moreover, the extent of the red heartwood column
was shown to be closely related to wound size (Shigo 1966; Hein 2008), so that the effect of
smaller branches might be limited (Eisner et al. 2002). The effect of SLR10 was not included
in the final model for yellow birch, even though this variable was associated with some of
the best candidate models.
Unlike in sugar maple, tree height had a significant positive effect on RHP in yellow birch.
This may reflect the fact that taller stems tend to have more branch scars. This result contrasts
with the findings of Giroud et al. (2008) and Wernsdorfer et al. (2006), but these studies
described the indirect effect of tree height through stem taper, rather than of tree height as a
stand-alone variable. In addition, they were both conducted on a restricted number of sites.
The significance of tree height in our study might also reflect the influence of other factors
such as soil properties or site fertility on the development of red heartwood, which we did
not directly consider.
At the stand scale, it is well-established that branch mortality is driven mainly by stand
density (Makinen 2002; Shmulsky and Jones 2011). Because high levels of tree-to-tree
competition normally lead to faster crown recession, it was expected that increased stand
basal area would stimulate red heartwood formation. However we found no evidence linking
stand basal area with RHP. This could reflect a trade-off between branch mortality and branch
size (i.e., the higher branch mortality in dense stands may be compensated for by their smaller
size).
The observed regional variation in RHP is in contrast with the study of Yanai et al. (2009)
who found no significant differences among six northern US states in sugar maple RHP. This
might be explained by the larger variations in growth conditions in the current study or to the
fact that variation in RHP is larger at the northern edge of the species distribution range. In
our study, the lowest daily minimum temperature over the year (LTMin) had a significant
effect on RHP in sugar maple, over and above the additive effects of age and radial growth.
LTMin was more closely associated with longitude than latitude, probably because of the
29
lower sampled range in the latter. Pither (2003) tested a climate-based hypothesis related to
the distribution range of a large sample of North American species and showed that low
extremes in temperatures (the lowest value of average daily minima during January) had a
significant limiting effect. Sakai and Weiser (1973) and Burke et al. (1976) obtained similar
results for other species. It is likely that sugar maple is more sensitive to extreme cold
temperatures than yellow birch because it has a more southerly distribution range (Godman
et al. 1990).
Low temperatures have often been associated with an irregular traumatic heartwood
formation called “blackheart” or “frost heart” (Burke et al. 1976; Taylor et al. 2002). Frost
heart formation episodes were reported in F. sylvatica, Acer species, and Fraxinus excelsior
L. after the severe European winters of 1928–1929 and 1941–1942, when temperatures fell
below –30 °C (Liese (1930) in Hillis (1987)). In sugar maple, the freezing resistance of the
xylem is –40 °C (Sakai and Weiser 1973). As some of the sites we sampled fall below this
threshold, it is possible that the negative relationship described between RHP and LTMin
could be related to increased proportions of frost cracks at these temperature extremes.
However, an attempt was made to limit the impact of these potentially confounding
observations by sampling only vigorous trees with no sign of such injuries.
Although further work is required to reach more conclusive explanations for regional
variations in RHP, the findings of this study provide useful insights for managers of northern
sugar maple and yellow birch hardwood forests. The best models for each species both had
a high predictive potential. There was limited improvement in the proportion of the variance
explained for each model between the fixed and random effects (i.e., from 60% to 67% in
sugar maple and from 60% to 65% in yellow birch). This suggests that there is limited
residual variance associated with random region and site effects. According to our results,
regional variation in discoloured wood proportion is most closely related to tree age and
growth-related variables. The strong positive effect of tree age on RHP implies that shorter
rotation lengths would be beneficial for appearance products. However, this may come at the
expense of the production of a defect-free bole (Shmulsky and Jones 2011). Our results
suggest that a promising strategy for forest managers would be to promote the regeneration
of dense cohorts in gaps created by partial cutting. A period without intervention would
30
promote crown recession and limit branch diameter. Once the desired length of clear bole is
reached, the best stems could be selected as crop trees and released (Perkey and Wilkins
1993). This would speed up the occlusion of dead branch stubs while maintaining the vigor
of live branches. In some situations, manual pruning could be considered at a young age, but
further studies are needed to assess the long-term effect and cost efficiency of this treatment
on heartwood proportion. In other instances, predictive models could be used to guide site
selection for timber or veneer production. Attention should be focused on extreme climatic
conditions and species range limits (Pither 2003; Burton et al. 2008). The unexplained
variation in the best model for each species might be associated with other factors, such as
soil type and genotypic variability, which should be considered in further studies. In addition,
supplementary investigations about healing rate and time to wound closure in hardwoods that
form traumatic heartwood are necessary for better understanding of the occurrence and
magnitude of red heartwood.
Conclusion
In this study, we tested the hypothesis that regional variations in RHP within stems of sugar
maple and yellow birch can be mainly explained by differences in tree age and growth-related
variables. A strong positive relationship between tree age and the proportion of discoloured
wood was observed for both species. A 5 year average of ring area increment at the limit of
the discoloured wood column was positively related to the RHP. Conversely, the growth
trend, expressed as the slope of the regression of ring area increments over a 5 year period
on either side of the discoloured wood boundary, was negatively related to the RHP in sugar
maple. These factors were interpreted as being related to the size and time before occlusion
of dead branches, which are known to act as initiation points for discolouration. In the case
of sugar maple, the lowest daily minimum temperature over the year also had a strong
negative effect on the RHP, over and above that of tree age and growth-related variables.
Overall, the fixed effects of the developed models were able to explain around 60% of the
variance in RHP for both species, and could be used to predict its regional variation and
inform forest management and wood procurement decisions. Further work should aim to
investigate the effects of soil characteristics and genetic factors on the proportion of red
heartwood within tree stems.
31
Acknowledgments
The authors are grateful to the Fonds de recherche du Québec – Nature et technologies
(FRQNT) for the financial support for this project. We wish to express our thanks to staff
from the Ministère des Ressources naturelles du Québec, Station touristique de Duchesnay
(SÉPAQ), and Groupement forestier de Portneuf for their help with locating sampling sites.
We are also grateful to Marine Bouvier, Stéphanie Cloutier, Simon Delisle-Boulianne,
Amélie Denoncourt, Élisabeth Dubé, Louis-Vincent Gagné, Louis Gauthier, Julia Maman,
and Marie-Pier Arsenault for their assistance in collecting the samples. Thanks are extended
to Rémi St-Amant and Jacques Régnière (Canadian Forest Service) for BioSIM
parameterization advice, to Marc J. Mazerolle for statistical advice, to David Auty for
grammatical revision of the manuscript, and to the anonymous reviewers for their valuable
comments on an earlier version of the manuscript. Special thanks to S.Y. Zhang who had the
original idea for this project.
33
Chapitre 2
Integrating standing value estimations into tree marking
guidelines to meet wood supply objectives2
2 Version intégrale d’un article publié / Intergral version of a published paper:
Havreljuk, F., Achim, A., Auty, D., Bédard, S. and Pothier, D. 2014. Integrating standing value estimations
into tree marking guidelines to meet wood supply objectives. Can. J. For. Res. 44(7), 750–759. doi:
10.1139/cjfr-2013-0407
34
Abstract
The identification of low-vigor trees with potential for sawlog production is a key objective
of tree marking guidelines used for partial cuts in northern hardwoods. The aim of this study
was to measure the impact of various vigor-related defects on the monetary value of
hardwoods. To achieve this, we sampled 64 sugar maple (Acer saccharum Marshall) and 32
yellow birch (Betula alleghaniensis Britton) trees from two locations in southern Quebec,
Canada. We identified over 420 defects, which were grouped into 8 categories. The trees
were then harvested and processed into lumber, and the value per unit volume of each stem
was calculated from the value of the product assortment (lumber, chips, and sawdust). We
found that visible evidence of fungal infections (sporocarps and (or) stroma) and cracks had
the largest negative influence on value in both species. A model that included these defects
was almost as good at predicting value as one that included a specifically designed quality
classification. A more accurate assessment of value could be achieved using wood decay
assessment tools and by considering site-specific variables. Results from this study showed
that visual identification of fungal infections and cracks could be used to enhance tree
marking guidelines for hardwoods. This would meet both the silvicultural objective of
selection cuts, by removing low-vigor trees, and the wood supply objective, by improving
stem quality assessment prior to harvest.
Key words: hardwoods, tree marking, defects, tree vigor, tree quality.
35
Résumé
L’identification des arbres moribonds qui ont un potentiel pour la production de billes de
sciage est un objectif clé des directives de martelage lors de coupes partielles dans les
peuplements de feuillus nordiques. Cette étude avait pour but de mesurer l’impact de divers
défauts reliés à la vigueur sur la valeur monétaire des feuillus. À cette fin, nous avons
échantillonné 64 érables à sucre (Acer saccharum Marshall) et 32 bouleaux jaunes (Betula
alleghaniensis Britton) à deux endroits dans le sud du Québec, au Canada. Nous avons
identifié plus de 420 défauts que nous avons regroupés en huit catégories. Ces arbres ont
ensuite été récoltés et transformés en sciage et la valeur par unité de volume de chaque tige
a été calculée à partir de la valeur de l’assortiment de produits (sciages, copeaux et sciures).
Nous avons constaté que les signes visibles d’infection fongique (sporocarpes ou stroma) et
les fentes avaient la plus grande influence négative sur la valeur des deux espèces. Un modèle
qui incluait ces défauts était presque aussi bon pour prédire la valeur qu’un modèle basé sur
un système de classes de qualité spécifiquement conçu. On pouvait obtenir une évaluation
plus précise de la qualité en utilisant des outils pour évaluer la carie du bois ou en tenant
compte de variables propres à la station. Les résultats de cette étude montrent que
l’identification visuelle des infections fongiques et des fentes peut être utilisée pour améliorer
les directives de martelage chez les feuillus. Cela devrait satisfaire tant les objectifs sylvicoles
des coupes de jardinage, en éliminant les arbres moribonds, que les objectifs
d’approvisionnement en bois, en améliorant l’évaluation de la qualité des tiges avant la
récolte.
Mots-clés : feuillus, martelage, défauts, vigueur des arbres, qualité des arbres.
36
Introduction
The natural disturbance regime of North American temperate deciduous forests is
characterized by mortality of individual trees, or group of trees, with very rare occurrence of
severe, large-scale disturbances (Seymour et al. 2002). To maintain the resulting uneven-
aged structure of the stands, selection cutting is often the preferred silvicultural system. Such
an approach aims to maintain or improve forest productivity by removing low-vigor trees,
which are expected to die before the next harvesting cycle (Arbogast 1957; Majcen et al.
1990; Nyland 1998). This strategy replaces several decades of management that focused on
selecting the best quality stems, which resulted in depleted stands (Nyland 1992). Under such
a system, the search for short-term profit is likely to conflict with the goals of sustainable
forest management.
The long-term success of selection cutting depends on making the appropriate choice of
stems that should be harvested. Under most tree marking systems, tree assessment is based
on the identification of defects that may affect both vigor and stem quality (Leak et al. 1987;
Majcen et al. 1990; OMNR 2004; Meadows and Skojac 2008; SWDNR 2013). In this study,
vigor is defined as the risk of tree mortality occurring before the next scheduled harvesting
cycle, and quality is defined with reference to the log and stem attributes that determine actual
and potential monetary value. When the criteria for assessing tree vigor are unclear or
misinterpreted, the objective of stand quality improvement associated with selection cutting
may be compromised (Bédard and Brassard 2002; Meadows and Skojac 2008).
Tree vigor assessment is a complex task that requires detailed knowledge of defects that
affect tree survival (OMNR 2004). Although tree vigor and quality are related concepts,
Fortin et al. (2009) showed that tree vigor, as assessed by the system of Boulet (2007), was
a poor predictor of log quality. This suggests that defects influencing the likelihood of tree
survival may not have an equivalent effect on stem value. To achieve the full production
potential of hardwood forests, an effective tree marking system should consider both
silvicultural and wood supply objectives for sustainable management. Thus, the harvesting
of non-vigorous trees that contain high quality sawlogs should be prioritized (Pothier et al.
2013).
37
One approach towards improving stem quality estimation when applying a tree vigor
evaluation system consists of using an additional standing tree classification (Hanks 1976;
Monger 1991). Like tree vigor assessment systems, existing hardwood stem quality
classification systems visually assess the presence, size, and distribution of defects along the
stem but focusing mainly on those that might affect conversion into wood products. In
addition to stem diameter, the quality class of each individual tree therefore depends mainly
on clear bole length (i.e., free of defects), curvatures, and cull deductions. Such rules are
consistent with log grade assessments (Rast et al. 1973; Petro and Calvert 1976), a fact that
was confirmed empirically by Fortin et al. (2009b). However, there is still little information
available about the specific factors that influence the product basket composition and
monetary value of hardwoods.
Drouin et al. (2010) showed that wood quality and value of white birch (Betula papyrifera
Marsh.) decreased when internal characteristics of the stem, such as discoloration and decay,
were considered. Detection and characterization of internal defects can therefore be improved
when non-destructive tools are used in combination with external visual inspection (Wang
and Allison 2008). Some tools, such as wood-drilling instruments (Costello and Quarles
1999; Barrette et al. 2013), are designed to detect the changes in wood density (i.e., internal
decay). Others use acoustic velocity (i.e., stress-wave propagation) to estimate wood
physico-mechanical properties (Wang et al. 2007; Paradis et al. 2013). However, data
acquisition using such tools may be expensive (Greifenhagen and Marilyn 2005; Leong et al.
2012), and their utilisation in classification systems for hardwoods remains to be evaluated.
For integration in tree marking, estimations of vigor and quality must be rigorous, yet
practicably applicable. For example, the integration of Monger’s (1991) tree grade
classification with Boulet’s (2007) vigor assessment would result in a 16-class system (4 × 4
matrix of vigor and quality grades), which would be difficult to apply operationally. The
objective of this study was thus to facilitate the integration of standing tree value estimations
into tree marking guidelines by identifying the main vigor-related variables affecting the
value of the product assortment from hardwood stems. This was applied to sugar maple (Acer
saccharum Marshall) and yellow birch (Betula alleghaniensis Britton) trees, which are the
dominant species in the hardwood forests of southern Québec, Canada.
38
Material and methods
Study sites
The study was conducted in two northern hardwoods forests located on public land in
southern Québec, Canada (Figure 2.1). The first site was located in Duchesnay (DU) near
Québec City, within the balsam fir (Abies balsamea [L.] Mill.) – yellow birch bioclimatic
domain. The second was located near Mont-Laurier (ML), in the Laurentian region, within
the sugar maple – yellow birch bioclimatic domain (Robitaille and Saucier 1998). According
to the climate estimations generated by BioSIM for the 1981–2010 period (Régnière et al.
2012), the mean and minimum annual temperatures are 3.2 °C and −36.5°C and 2.3 °C and
−41.2 °C, for the DU and ML sites, respectively.
Figure 2.1 Location of the study areas.
At DU, total annual precipitation is 1368 mm with about 33% falling as snow, while at ML
it is 1013 mm with 34% as snow. Both stands had an approximate area of 50 ha. The total
basal area (BA) of merchantable standing trees was 23.5 m² ha −1 for the DU site and 25.0
m² ha−1 for the ML site. At the DU site, sugar maple and yellow birch represented 38% and
39
36% of total BA, respectively, while the remaining BA was composed of American beech
(Fagus grandifolia Ehrh.). The ML site was dominated by sugar maple (87% of total BA),
followed by yellow birch (6%), American beech (5%), and red maple (Acer rubrum L.) (2%).
Soils at both sites were moderately to well-drained glacial tills.
Sampling
A sample of 64 sugar maple and 32 yellow birch trees, equally distributed between the two
sites, was selected. To ensure that a wide range of tree vigor and quality combinations were
included, the sampling was stratified according to a matrix of vigor and quality classes
provided by Boulet (2007) and Monger (1991), respectively.
The tree vigor classification system aims to identify stems with the highest risk of dying
before the next cutting cycle. Harvest priority is based on the signs and symptoms of more
than 250 observable defects, which are grouped into eight categories: (1) fungal infection
(through observations of visible sporocarps and stroma on the stem), (2) cambial necrosis,
(3) bole deformations and injuries, (4) butt and root defects, (5) stem and bark cracks, (6)
woodworms and sap wells, (7) crown defects, and (8) branching and pruning defects.
Depending on the presence and severity of the observed defects, trees are ranked into four
harvest priorities: (1) moribund trees (M), (2) surviving trees (S), (3) growing trees to be
conserved (C), and (4) reserve stock trees (R). Moribund trees are expected to die before the
next cutting cycle, while S trees are defective and declining but are assumed to survive until
the next harvest. Class C corresponds to growing trees with minor defects, while reserve trees
are those without defects and with the highest survival probability that should be retained in
the stand.
Standing tree quality assessment was achieved using Monger’s (1991) classification. Four
grades (A, B, C, and D) are used to describe stem potential for producing sawlogs, where the
highest tree quality corresponds to grade A and the lowest to grade D (i.e., trees with no
sawlog potential). This classification is based mainly on stem size and on the observable
defects on the lower 5 m of the tree. Trees must meet minimum diameter at breast height
(DBH, 1.3 m above ground level) thresholds for each grade (A > 39 cm, B > 32 cm, C and
D > 23 cm). The quality assessment consists of first identifying the “best” 3.7 m stem section
40
within the lower 5 m of the stem (i.e., the section with the fewest defects). Then, the chosen
section is separated into four equal faces circumferentially, to estimate the clear wood yield
of each face. For each tree, a quality grade is assigned according to the clear wood length of
the third-best face and the estimated percentage reduction in volume due to observable cull,
rot, cracks, and sweep measured in the whole stem section. These rules were derived from
the tree grading system developed by Hanks (1976).
Tree selection
To complete the sampling matrix, trees were initially classified according to the two systems
described above. The assessments were limited to stems with a DBH greater than 23 cm,
which is considered the lower merchantable limit. To incorporate stem size heterogeneity,
trees were randomly selected from two DBH categories for each quality–vigor combination
(i.e., under and over 46, 40, and 34 cm for grades A, B, and C-D, respectively). At each site,
one yellow birch and two sugar maple sample trees were randomly selected from each
quality-vigor combination, giving a total of 32 and 64 sample trees, respectively, for each
species across the two sites. At the DU site, some specific combinations were not found inside
the study area. In these cases, two missing grade A trees for each of the M and S vigor classes
were replaced by two B quality trees. To ensure the accuracy of sample tree assessment, all
vigor and quality evaluations were verified and approved by certified and trained tree
markers. A summary of the mean sample tree characteristics is presented in Table 2.1.
Sample tree measurements
On each sample tree, the position and size of all observable defects were determined using a
measuring tape on the lower 5 m section of the stem and a hypsometer (Vertex IV Ultrasonic
Hypsometer, Haglöf AB, Sweden) in the upper part. Total tree height (m), the height of the
first living branch (m), and the height of the main fork or primary branches (m) were also
measured using a hypsometer.
41
Table 2.1 Mean sample tree characteristics for the sugar maple and yellow birch data.
No. of stems Mean DBH ±SD [range]
(cm)
Mean height ±SD
(m)
Mean gross merchantable
volume ±SD (dm³)
Sugar maple 64 38.4 ±7.6 [23.5-58.5] 21.7 ±2.5 1093 ±530
M 16 38.7 ±6.9 [29.3-50.1] 21.4 ±2.2 1073 ±433
S 16 38.6 ±9.1 [23.5-58.5] 21.7 ±2.6 1136 ±692
C 16 38.3 ±7.2 [26.2-55.0] 21.8 ±2.6 1098 ±533
R 16 37.8 ±7.7 [24.6-50.5] 21.9 ±2.7 1063 ±477
Yellow birch 32 39.1 ±7.9 [26.6-62.4] 22.4 ±2.2 1216 ±572
M 8 43.4 ±10.4 [29.9-62.4] 21.5 ±1.8 1471 ±823
S 8 39.3 ±6.5 [28.6-48.3] 23.7 ±1.7 1272 ±439
C 8 35.8 ±7.3 [26.6-46.9] 21.0 ±2.5 958 ±480
R 8 38.0 ±6.0 [31.0-47.5] 23.3 ±2.0 1163 ±434
Total 96 38.6 ±7.7 [23.5-62.4] 21.9 ±2.4 1134 ±544
Note: Trees are classified by harvest priorities: moribund trees (M), surviving trees (S), growing trees to be
conserved (C), and reserve stock trees (R) (Boulet 2007).
An evaluation of the internal decay of all study trees was performed using the wood-drilling
instrument Resistograph F-500SE (Instrumenta Mechanik Labor System GmbH (IML),
Germany). This device measures the resistance to drilling in a tree. In the presence of decay
and cavities into the stem, drilling resistance decreases (Mattheck et al. 1997), and the extent
of these defects can be estimated. In this study, two perpendicular drillings were made at 1.3
m above ground level (Greifenhagen and Marilyn 2005). Resistograph readings were
analyzed following the general principles described by Mattheck et al. (1997). To simplify
their visual interpretation, readings were categorized into two classes: sound wood and
decayed wood, the latter characterized by a decrease in wood density caused by cavities and
cracks. Two perpendicular drilling profiles were fully obtained on each tree. The depth of
sound wood (Costello and Quarles 1999) was used as a potential predictor variable in the
subsequent analyses, as it is closely related to the number and size of high grade lumber
pieces. This was calculated as the amount of non-decayed wood from the inner bark to the
first decayed point, averaged from four radii around the tree (i.e., two complete linear
drillings). Fourteen trees (13 sugar maple and one yellow birch) had incomplete radial profile
readings due to either large stem size or the presence of major defects. For those trees, the
analyses were made using only the complete radii (i.e., cambium to pith).
42
Standing tree quality of sugar maple and yellow birch was also evaluated using acoustic
measurements. Acoustic velocity in wood can be used to estimate its physico-mechanical
properties (Kumar 2004; Wang and Allison 2008). Generally, sound waves propagate more
slowly in a damaged or decayed wood than in sound wood (Leong et al. 2012). We used the
IML Hammer (Instrumenta Mechanik Labor (IML) GmbH, Germany) to obtain radial
velocity measurements. The general approach consisted of generating a sound wave by
hammer impact on a probe located on one side of the stem at 1.3 m above ground level. The
resulting dilatational wave traveled to the other side of the stem where a receiving probe was
located. Acoustic velocity was taken as the ratio of the distance between the probes to the
transit time. The average of two perpendicular measurements was used for each tree. In both
sites, trees were measured by the same person to minimize any potential operator bias.
Tree felling and bucking
Felling operations were conducted in the fall of 2009 and 2010 at the DU and ML sites,
respectively. Full-length trees were harvested and efforts were made to minimize logging
damage on the sample trees and to preserve any large branches with sawing potential. Felled
trees from each site were transported to the Duchesnay sawmill (Sainte-Catherine-de-la-
Jacques-Cartier, Québec), where they were inspected and cut into logs according to the Petro
and Calvert (1976) grading rules. At this stage, we included an additional sawlog category to
accommodate small diameter logs (bolts) (Bumgardner et al. 2001), thus ensuring the full
potential value of each tree was obtained (Giguère 1998). Efforts were made to identify
veneer logs, but these were combined with sawlogs in subsequent analyses because they
occurred very rarely.
Sawmill conversion
A total of 128 logs were sawn at the Duchesnay sawmill, while 61 bolts were transformed
using a portable sawmill (Wood-Mizer Products Inc., USA) at Laval University’s wood
research center. All logs were sawn using a grade sawing approach (Richards et al. 1979),
which consists of maximizing the production of high-grade lumber (i.e., knot-free sapwood)
by rotating the log around its pith (Steele 1984). For consistency, logs from both study sites
were sawn by the same qualified workers. A total of 2236 boards were produced, and their
43
provenance (i.e., tree and log) was traced during the conversion process. Lumber pieces were
all standard 2.54 cm thick (1 inch), with variable widths and lengths ranging from 7.6 to 35.6
cm (3 to 14 inches) and 1.22 to 3.62 m (4 to 12 feet), respectively. Each board was graded
according to the standards of the National Hardwood Lumber Association (2011). The initial
step in the lumber grading was to determine the number of board feet in each piece. One
board foot (2360 cm³ ) is the equivalent of a board measuring 30.48 cm long × 30.48 cm wide
× 2.54 cm thick (1 foot × 1 foot × 1 inch). For both species, standard grades were divided
into several quality classes (FAS, F1F, Selects, No. 1 Common, No. 2A Common, No. 3A
Common, and No. 3B Common), which are mainly related to the size of clear face cuttings.
The best grade is FAS, and the lowest is No. 3B Common, which in practice corresponds to
pallet lumber. Boards of a lower quality than this grade were rejected. In addition, board
color was also assessed, as it can affect lumber prices. According to NHLA (2011) rules,
sugar maple boards were classified as No. 1 White Maple, No. 2 White Maple, or Sap,
depending on the extent of sapwood on the faces and edges of cuttings. For yellow birch, the
color premium could either be associated with non-colored wood (Sap birch) or discolored
heartwood (Red birch), as long as it was uniform. For consistency, boards from both sites
were graded by the same qualified inspector. The distribution of boards is presented in Table
2.2 and 2.3.
44
Table 2.2 Lumber grade distribution among the sawn boards.
NHLA grades Total no. of
boards
No. of board
feet % of board feet
Sugar maple 1460 5469 100.0
FAS 61 372 6.8
F1F 61 370 6.8
SEL 98 348 6.4
1C 265 1029 18.8
2A 324 1160 21.2
3A 252 850 15.5
3B 399 1340 24.5
Yellow birch 776 2989 100.0
FAS 51 307 10.3
F1F 39 214 7.2
SEL 61 239 8.0
1C 182 731 24.5
2A 178 609 20.4
3A 120 397 13.3
3B 145 492 16.5
Note: FAS represents the best grade and No. 3B Common (i.e., pallet lumber) the lowest.
Table 2.3 Distribution of NHLA grades among tree quality classes.
Tree quality
classes
NHLA Grades (% of board feet)
FAS F1F SEL 1C 2A 3A 3B
Sugar maple
A 7.5 8.5 6.8 23.1 20.8 13.5 19.7
B 9.1 7.9 6.3 17.9 21.7 14.7 22.3
C 1.8 3.8 7.4 14.5 19.6 19.5 33.3
D 2.0 0.0 2.9 16.6 23.3 19.5 35.8
Yellow birch
A 16.3 11.3 4.4 28.3 17.8 10.0 11.9
B 7.2 3.8 11.5 24.5 21.7 12.4 18.9
C 2.3 1.4 11.8 14.2 23.3 22.1 24.9
D 0.0 8.5 7.8 27.0 26.2 16.3 14.2
Note: Grade A is the highest quality, while grade D is the lowest (i.e., trees with no sawlog potential).
Value estimations
Lumber value estimations
Lumber value for sugar maple and yellow birch was determined using Hardwood Market
Report (2008–2012) price lists for northern hardwoods. A five-year average price (2008 to
2012) was used for rough green wood (US dollars per 1000 board feet – MBF) (Table 2.4).
45
The value of each piece was obtained according to its NHLA grade and board size. For
consistency with the lumber value of each grade, the F1F and FAS grades were combined,
as were the No. 1 and No. 2 White Maple color grades.
Table 2.4 Mean sugar maple and yellow birch lumber values from 2008 to 2012.
NHLA grades Hard maple Birch
Unselected Sap No. 1&2 White Unselected Red Sap
FAS 1195 1295 1420 1105 1410 1380
Selects 1175 1275 1400 1085 1390 1360
No. 1C 760 860 860 685 990 960
No. 2A 540 640 640 430 735 705
No. 3A 355 455 – 280 585 555
No. 3B (pallet) 225 – – 225 – –
Note: Values are presented in US$ per MBF for 2.54 cm thick (1 inch) boards of random widths and lengths
that are rough and green. 1000 board feet (MBF) = 2.36 m³.
Pulpwood value estimations
Pulpwood prices vary widely among buyers, tree species, and location. For simplicity, it was
estimated at 40 USD per cubic meter (solid), delivered to the mill (i.e., includes harvesting
and hauling). This represents the estimated 2008 to 2012 average pulpwood value reported
for the northeastern area of North America (NC State University 2013; SPFRQ 2013). The
same value was used for both sugar maple and yellow birch trees, as they are generally sold
together as mixed hardwoods. The estimated pulpwood value was applied to all the pulpwood
logs (i.e., pieces over 2.5 m long and with a top diameter over 9 cm inside bark) in our study
that did not produce any sawn lumber, while waste logs were omitted from the study since
they constituted a negligible proportion of the total. To incorporate wood chips and sawdust
into estimations of tree value per cubic meter, a pulpwood price of 40 USD per cubic meter
was assigned to the difference between the net round wood volume of each log and the total
volume of lumber produced.
Tree value estimations
The estimated value per unit volume (VAL) of each stem, which was the dependent variable
in this study, was expressed in US dollars per cubic meter of round wood ($·m−3 ). This was
estimated by dividing the sum of values from each product by the gross volume of the stem.
46
The latter was derived from a volume equation using DBH and total tree height as predictors
(Perron 2003). VAL was preferred to total stem value, because it is less influenced by tree
size and it corresponds to the units used in the industry for log procurement.
Statistical analysis
In line with the general objective, statistical analysis was used to study the links between the
visual criteria included in the classifications of standing trees and their value per cubic meter
(VAL). The influence of tree classification systems on value was tested using analysis of
variance (ANOVA). When significant differences were found, multiple comparisons were
carried out to discriminate between each class. This was performed using Tukey’s honestly
significant difference test (Tukey HSD), with a robust procedure used to account for the
unbalanced nature of the data (Herberich et al. 2010). Differences between means were
considered significant at a value of p < 0.05. To build a predictive model of VAL, the first
step consisted of determining the relationship between VAL and DBH. Several equations
were tested and an exponential function (eq. (1)), previously described by Barrette et al.
(2012), was chosen as it provided the best fit to the data:
(1) 𝑉𝐴𝐿 = 𝑏1𝐷𝐵𝐻𝑏2𝑏3𝐷𝐵𝐻
where b1, b2 and b3 are the model parameters to be estimated. To facilitate the integration of
other covariates in this model, this equation was linearized through a log-transformation
process, as follows:
(2) ln(𝑉𝐴𝐿) = 𝑏1′ + 𝑏2 ln(𝐷𝐵𝐻) + 𝑏3
′ 𝐷𝐵𝐻
where ln(VAL) represents the natural logarithm of VAL and the indices refer to linearized
parameters from Eq. (1).
Analyses of variance were conducted to assess the effect of each of the eight defect categories
described by the vigor classification on VAL. Both discrete (presence/absence) and
continuous (number and size) variables for each defect category were tested. In this step, we
also considered potential interactions between defect classes and DBH. Defects that had a
significant effect on VAL were included in the model as follows:
47
(3) ln(𝑉𝐴𝐿) = 𝑏1′ + 𝑏2 ln(𝐷𝐵𝐻) + 𝑏3
′ 𝐷𝐵𝐻 + 𝑏′𝑍
where Z represents the additional covariates in the final model described below.
Model selection
To test the effectiveness of stand- and tree-level characteristics for predicting tree value per
unit volume, models of increasing complexity were successively fitted to the data. Several
combinations of variables were screened in the models. First, a null (i.e., intercept-only)
model was fitted, to be used as the reference level for the more complex models. Next,
variables relating to site- and tree-level characteristics were added, followed by variables
relating to tree classification (i.e., vigor, quality, and defects). Finally, variables obtained
using non-destructive methods (i.e., Resistograph and IML-Hammer) were assessed. In total,
fifteen candidate models were developed and compared using the corrected Akaike
information criterion (AICc) and Akaike weights (wi), which assess the relative likelihood of
each model across all candidate models (Burnham and Anderson 2002; Anderson 2008). In
addition, fit indices (R²) were calculated for each model, but these were not used as a criterion
for model selection.
All candidate models were checked for error normality, homogeneity of variance, and the
influence of extreme values. Multicollinearity between variables was checked using the
variance inflation factor (VIF) (Zuur et al. 2010), with an upper limit value of 5 if variables
were to be included in candidate models. Predicted values of log-transformed equations were
corrected for bias using Sprugel’s (1983) correction factor. All statistical analyses were
performed using libraries contained in the R statistical programing environment (R Core
Team 2013).
Results
Effect of vigor and quality on tree value
Multiple comparisons between vigor classes (M-S-C-R) revealed that differences in VAL
were only significant between the M and R vigor classes (p = 0.004). A similar result was
48
observed when the model (eq. (3)) included both the vigor classification and DBH. M trees
were less valuable than R trees (Figure 2.2). In contrast, significant differences in VAL were
observed among all quality classes (A–C: p = 0.012; A–D: p = <0.001; B–C: p = 0.018; B–
D: p = < 0.001; C–D: p = 0.012), except between the A and B classes (p = 0.977). When the
quality classes were combined with DBH in eq. (3), predicted tree value per unit volume
decreased, as expected, from class A to class D (Figure 2.3). Overall, VAL was inversely
correlated with tree diameter in the A and B quality classes. There was a lower correlation
between VAL and DBH for the C and D classes, although the highest values tended to occur
at a DBH of about 35 cm. Since no significant differences were found between the study
species, data for sugar maple and yellow birch were combined in the remaining analyses.
Figure 2.2 Predicted VAL (US$·m−3) in relation to vigor classification. Trees are classified
by harvest priorities: moribund trees (M), surviving trees (S), growing trees to be conserved
(C), and reserve stock trees (R) (Boulet 2007).
49
Figure 2.3 Predicted VAL (US$·m−3) in relation to quality classification. The four grades (A,
B, C, and D) are used to describe the potential for sawlog production, with grade A being the
highest and grade D the lowest (i.e., trees with no sawlog potential) (Monger 1991).
Influence of defects on tree value
More than 400 defects associated with the tree vigor classification were identified on our
sample trees (Table 2.5). Of the eight categories of defects that are considered in tree marking
classification systems, two had a significant effect on VAL. The presence of both fungal
infection and cracks were negatively correlated with tree value per unit volume. In the former
case, the effect was greater in larger stems (result not shown). When both these variables
were included in the same model along with DBH, and with the inclusion of an interaction
term between DBH and fungal infection, the AICc was reduced compared to models that did
not include defects (Table 2.6 and Figure 2.4). In addition to the presence or absence of
defects, the inclusion of the raw counts of defects in the models was also tested, but in each
case there was no significant reduction in AICc. In addition, cracks longer than 1.5 m that
were associated with decay appeared to have a greater effect on tree value than shorter cracks
with no decay, but differences were not significant (results not shown).
50
Table 2.5 Proportion of study trees (%) affected by a given defect category.
Site Defect group
1 2 3 4 5 6 7 8
Duchesnay 5.2 6.3 10.4 10.4 37.5 6.3 25.0 33.3
Sugar maple 3.1 2.1 8.3 7.3 26.0 5.2 17.7 22.9
Yellow birch 2.1 4.2 2.1 3.1 11.5 1.0 7.3 10.4
Mont-Laurier 10.4 8.3 18.8 7.3 39.6 11.5 12.5 14.6
Sugar maple 7.3 5.2 12.5 3.1 29.2 11.5 10.4 7.3
Yellow birch 3.1 3.1 6.3 4.2 10.4 0.0 2.1 7.3
Note: Proportions do not sum to 100% because individual trees can exhibit several defects simultaneously.
Categories of defects were as follows: fungal infection (1), cambial necrosis (2), bole deformations and injuries
(3), butt and root defects (4), stem and bark cracks (5), woodworms and sap wells (6), crown defects (7), and
branching and pruning defects (8).
Table 2.6 Parameter estimates (± SE) and p-values for the model including DBH, fungal
infections, and cracks given by eq. (3).
Parameter Variable Estimate SE P-value
b’1 Intercept -12.532 5.116 0.016
b2 ln(DBH) 6.237 1.933 0.002
b’3 DBH -0.147 0.050 0.004
b’4 Fungi 1.086 0.806 0.181
b’5 Crack -0.335 0.118 0.006
b’6 DBH*Fungi -0.044 0.020 0.032
Fit statistics
n 96
R² 0.303
RSE 0.483
Bias 1.124
Note: n is the number of observations, R² is the coefficient of determination, RSE is the residual standard error,
and Bias is equal to e(RSE^2/2).
51
Figure 2.4 Predicted VAL (US$·m−3) of sugar maple and yellow birch in relation to the
presence of the main tree defects.
Final model for predicting tree value
The ranking of the fitted models, based on AICc, is presented in Table 2.7. These results
revealed that the utilization of wood decay assessment tools could improve tree value
predictions. The best model for predicting VAL in sugar maple and yellow birch included
the variables site, DBH, quality classification, and Resistograph readings (model 14; AICc =
77.9, wi = 0.97). The next best was model 15 (AICc = 85.0, wi = 0.03), which included site,
DBH, fungal infections, cracks, and Resistograph readings. Under the model ranking criteria
(AICc and Akaike weights), these models were considerably better than all the other
candidate models (Table 2.7). The adjusted R² of model 14 and model 15 were 0.65 and 0.63,
respectively. The effect of sound wood depth, as measured by the Resistograph, on stem
value per unit volume is presented in Figure 2.5 for quality classification and Figure 2.6 for
fungal infections and cracks.
Among the simpler alternatives, the model that included fungal infection, cracks and DBH
(model 7; AICc = 142.0) was also very similar, in terms of AICc, to the model that included
both quality classification models and DBH (model 6; AICc = 141.8). In comparison, the
52
model that included vigor classification and DBH performed poorly (model 5; AICc = 158.0).
The analysis also highlighted important differences in tree value between the two
experimental sites, since its inclusion as a predictor variable improved the fit of all models.
Table 2.7 Comparison of the linearized models for predicting the value per unit volume
(VAL) of each stem.
Model
group ID Explanatory variables Rank K AICc ∆i wi LL Adj. R²
Intercept 1 Null 15 2 170.7 92.8 0.0 -83.3 0
Site 2 Site 12 3 153.7 75.9 0.0 -73.7 0.17
Tree 3 DBH 14 4 166.9 89.0 0.0 -79.2 0.06
4 DBH + Site 11 5 145.6 67.7 0.0 -67.5 0.26
Tree +
Classifications
5 DBH + Vigor 13 7 158.0 80.2 0.0 -71.4 0.18
6 DBH + Quality 9 7 141.8 63.9 0.0 -63.3 0.30
7 DBH * Fungi + Cracks 10 7 142.0 64.1 0.0 -63.3 0.30
8 DBH + Vigor + Site 8 8 131.8 53.9 0.0 -57.1 0.38
9 DBH + Quality + Site 3 8 110.1 32.3 0.0 -46.2 0.51
10 DBH * Fungi + Cracks + Site 6 8 122.2 44.3 0.0 -52.3 0.44
Tree +
Classifications
+ Non-
destructive
evaluation
11 DBH + Quality + Resistograph 5 8 118.8 41.0 0.0 -50.6 0.46
12 DBH + Quality + Acoustic 7 8 126.7 48.8 0.0 -54.5 0.41
13 DBH * Fungi + Cracks + Resistograph 4 8 116.4 38.5 0.0 -49.4 0.47
14 DBH + Quality + Resistograph + Site 1 9 77.9 0.0 0.97 -28.9 0.65
15 DBH * Fungi + Cracks + Resistograph + Site 2 9 85.0 7.1 0.03 -32.4 0.63
Note: Rank is the model ranking according to the AICc, K is the total number of parameters (including the
model intercept), ∆i is the difference between the AICc and that of the best model, wi is the ratio of the ∆i for a
given model to that of the whole set of candidate models, LL is the log-likelihood. NB: DBH corresponds to
DBH + ln(DBH), except for the interaction with fungi, where it represents DBH * Fungi + ln(DBH).
53
Figure 2.5 Predicted VAL (US$·m−3) in relation with sound wood depth for quality
classification (Monger 1991).
Figure 2.6 Predicted VAL (US$·m−3) in relation with sound wood depth for main defects.
54
Discussion
Tree marking systems for hardwoods must meet both silvicultural and wood supply
objectives while remaining practically applicable. This study confirmed that a tree marking
system based on tree vigor, such as the one currently used in Quebec, is poorly related to the
standing value of sugar maple and yellow birch trees. These results are in agreement with
those of Fortin et al. (2009b), who have demonstrated the low ability of the same
classification system to determine log grades in standing trees. We argue that it would be
possible to improve tree selection by discriminating based on vigor-related variables that also
affect tree value. Of these, our results show that visible signs of fungal infections (i.e.,
sporocarps and (or) stroma) and cracks are the main variables that affect the current market
value of sugar maple and yellow birch stems. Therefore, trees that are affected by other types
of defects, such as cambial necrosis, stem deformations, mechanical injuries, woodworms,
sap wells, or crown and branching defects, might have a low probability of survival with no
appreciable loss of value. Therefore, our results suggest that these stems should be prioritized
for harvest to achieve both the main silvicultural objective, by removing low-vigor trees, and
the wood supply objective of selection cuts (Leak et al. 1987; Majcen et al. 1990; Nyland
1998; Pothier et al. 2013). Statistically, the use of Monger’s (1991) quality classification
brought only a marginal improvement over the alternative model that simply considered the
presence of fungal infections and cracks. In forest surveys intended to establish a more
precise estimate of standing tree value, quality classification, with the potential addition of
data from wood decay assessment tools, should be preferred (Model 11, Table 2.7). However,
because of the need for simplicity and cost-effectiveness, we recommend the use of the model
based on the presence of fungal infections and cracks in hardwood tree marking operations
(Model 7, Table 2.7).
In this study, visible evidence of fungal infections was one of the main vigor-related variables
affecting standing tree value per unit volume. These are known to be related to a higher
probability of stem mortality (Guillemette et al. 2008) and are usually associated with
decayed wood (Lavallée and Lortie 1968; Boulet 2007). The effect of fungal infections on
tree value increased with stem diameter, probably because larger trees are generally older
and contain a greater proportion of decayed wood (Basham 1991). The reduction in tree value
55
was greatest when both fungal infections and cracks occurred simultaneously on the tree
(Figure 2.4). While the incidence of frost cracks has been associated with larger trees (Burton
et al. 2008), we did not observe an interaction between cracks and stem diameter in our study.
Cracks are often associated with undesirable internal characteristics, such as discoloration or
decay (Shigo 1966; Lavallée and Lortie 1968), which in turn may decrease the value of raw
material designated for appearance wood products (Wiedenbeck et al. 2004).
In our study, tree value per unit volume decreased with dbh even in stems in the A and B
quality classes, i.e., those that are virtually free of external defects. Since the value was
expressed in terms of volume, this suggests that lumber yield was lower in larger stems. In
southern Appalachian species, Prestemon (1998) also observed that the probability of
obtaining higher quality grades tended to decrease in large trees. In our study, the maximum
value for both species was reached at DBH values between 40 and 45 cm. This is less than
the optimal DBH observed by Pothier et al. (2013), where the joint probability of obtaining
both low-vigor and high quality trees was highest at around 58 and 64 cm for sugar maple
and yellow birch, respectively. However, the latter study grouped all trees of Monger’s
(1991) A, B, and C classes into a “high quality” category (i.e., trees likely to contain at least
one sawlog). In the current study, the decreasing value of large standing trees of the highest
quality grades indicates that a decline in quality can occur even in the absence of external
signs of degradation (Shigo 1984). The larger trees in a stand are likely to have progressively
accumulated internal defects over time, such as heartwood discoloration, resulting in loss of
quality (Erickson et al. 1992; Baral et al. 2013). This suggests that diameter thresholds could
be included in tree marking criteria to avoid financial losses due to this potential degradation.
While the exact diameter limits still need to be determined, results reported by Hansen and
Nyland (1987) indicate that sawn timber volume and value from sugar maple decline in stems
over 50 cm in diameter. For sugar maple, Majcen et al. (1990) suggested a maximum
diameter of between 45 and 60 cm, depending on site quality, while Leak et al. (1987)
suggested a maximum of 40 to 50 cm.
Unsurprisingly, the inclusion of variables associated with the extent of the decay in the stem
tended to improve value estimations in our models. Of these, Resistograph readings gave
more accurate estimations of tree value than acoustic velocity measurements. In fact, the
56
coefficient of determination (R²) increased by around 15% when the depth of sound wood
was included in the models, compared with models with no Resistograph measurements.
Wood-drilling instruments have already proven their utility in tree-risk assessment (Costello
and Quarles 1999; van Wassenaer and Richardson 2009). However, the high cost of data
acquisition for these methods (Greifenhagen and Marilyn 2005; Leong et al. 2012) might
only be justified either in circumstances where knowledge of the internal wood properties of
specific trees is required or where regional-scale assessments of the variation in wood quality
are desirable (Moore et al. 2009; Barrette et al. 2013).
The analysis revealed that there were important differences in standing tree value between
the sites used in this study. The significance of the site effect remained even when it was
combined with the wood decay assessment variables in the models, suggesting that some
among-site variability might be attributable to internal defects that were not characterized by
the tested devices. For instance, the proportion of discolored wood, which is known to vary
with tree growth rate and tree age at the regional scale (Havreljuk et al. 2013), may also vary
significantly between sites. However, more study sites are required to quantify the true site-
to-site variability in standing tree value.
It must be pointed out that our study assessed standing tree value in terms of traditional end-
products. While stems without fungal infection and cracks may represent the best financial
opportunity for lumber industries, those affected by such defects might have some potential
for other end-uses, such as wood extractives (St-Pierre et al. 2013) or bioenergy (Lestander
et al. 2012). In addition, the retention of low-vigor, low quality trees in the residual stand
must be envisaged, as these can bring further benefits to forest ecosystems, including the
provision of habitat for important plant and animal species (Leak et al. 1987; Kenefic and
Nyland 2007). However, clear guidelines would have to be developed to avoid the ever-
present risk of high-grading hardwood stands. Additionally, the contamination risk to the
residual stand from low-vigor trees with various defects is still to be addressed (Horsley et
al. 2002; Fortin et al. 2013).
After a selection cut, the residual stand should be composed of vigorous trees that are likely
to improve in grade over time (Leak et al. 1987; Bastien and Wilhelm 2000). Although the
57
results of our study could be used to integrate stem quality considerations into Boulet’s
(2007) classification, our data does not allow for an evaluation of the vigor classes used in
this system. Yet, Hartmann et al. (2008) have suggested that it could be simplified further.
The authors found that trees from the lowest vigor class (M class) have a greater probability
of dying than high-vigor trees (R class), but there were no differences between the
intermediate vigor classes, suggesting that a vigor assessment needs just two categories (i.e.,
mortality and survival). Thus, a potential simplification of both the quality and vigor
classifications might result in a four-class hybrid system representing vigorous and non-
vigorous trees, with or without sawing potential. Comparable systems containing two to six
classes are already in use in parts of North America (Arbogast 1957; Leak et al. 1987; OMNR
2004; Meadows and Skojac 2008; SWDNR 2013). This approach would be similar to that of
Majcen et al. (1990), which has been previously applied in Quebec, although it would be
based on a more detailed description of stem defects. However, as Boulet’s (2007) tree
classification system was implemented in 2005, further studies will be required to evaluate
its applicability for predicting tree death, or to include potential simplifications to the
assessment of vigor.
Conclusion
The objective of this study was to improve a tree marking system focusing only on tree vigor
by identifying the main variables that affect the monetary value of hardwood stems. The
effectiveness of the current marking system for predicting standing tree value was found to
be low. The identification and quantification of various types of defects on sugar maple and
yellow birch stems showed that fungal infections (i.e., visible sporocarps and (or) stroma)
and cracks are the main factors that affect stem value. Predictive models of standing tree
value using these variables performed almost as well as more complex models that included
a full standing tree quality classification in the predictors. We conclude that enhanced tree
marking guidelines, based on the visual identification of fungal infections and cracks, would
be both practical to apply and less costly than the inclusion of a comprehensive stem quality
assessment. The proposed amendments may help achieve both the silvicultural objective of
selection cuts, by removing low-vigor trees, and the wood supply objective, by improving
quality assessment in standing trees.
58
Acknowledgements
This study was financially supported by the Fonds de recherche du Québec – Nature et
technologies (FRQNT). The authors are grateful to the staff from the Ministère des
Ressources naturelles du Québec, Station touristique de Duchesnay (SÉPAQ) and
Coopérative Forestière des Hautes-Laurentides (CFHL) for providing and harvesting the
sampling sites. We wish to express our thanks to staff from École de foresterie et de
technologie du bois de Duchesnay for their valued collaboration in this project. We also thank
Frauke Lenz, Élisabeth Dubé, and Jean-Philippe Gagnon for their assistance in field work,
Jocelyn Hamel, Étienne Boulay, and Roch Boulerice for tree grading validation and to Julie
Barrette, Emmanuel Duchateau, and Normand Paradis for their help during the sawmill trial.
Thanks are extended to the staff of Centre de recherche sur le bois (CRB – Laval University)
and FPInnovations for their assistance in this project.
59
Chapitre 3
Predicting lumber grade occurrence and volume
recovery in sugar maple and yellow birch logs
60
Abstract
Forest production from the North American temperate deciduous forests is mainly associated
with the processing of hardwoods by the appearance wood products industries. To improve
the supply decisions for these industries, it is important to understand the factors that affect
the manufactured products assortment from trees and logs. The objective of this study was
to investigate and model the relationship between log characteristics and sawn board
attributes in sugar maple (Acer saccharum Marshall) and yellow birch (Betula alleghaniensis
Britton). We harvested 64 sugar maple and 32 yellow birch trees from two locations in
southern Quebec, Canada, which were processed into sawlogs, prior to being converted into
lumber. A total of 2236 boards were assessed for grades and colors specifications according
to the rules of the National Hardwood Lumber Association (NHLA). We developed statistical
models taking into account the high proportion of zeros in the data, for predicting the volume
recovery of the various lumber grades and color specification. In both species, board grades
were strongly related to the log length, the position of the log in the stem, the small-end
diameter of the log and the diameter of decay at the small-end of the log. Lumber color was
related to the net volume of the log and red heartwood volume for sugar maple, and to the
log length, the small-end diameter of the log and the red heartwood diameter at the large-end
of the log for yellow birch. These models outperformed a specifically designed log
classification system in predicting the lumber volume recovery. From a management point
of view, the production of valuable lumber should focus on the butt log and could be achieved
by promoting a fast radial growth of the stem, thereby limiting the development of red
heartwood.
61
Résumé
La production forestière dans les forêts feuillues tempérées d’Amérique du Nord est
principalement associée aux industries des produits d'apparence en bois. Afin d’améliorer les
décisions d'approvisionnement de ces industries, il est important de comprendre les facteurs
qui influencent le panier de produits provenant d'arbres et de billes. L'objectif de cette étude
était de modéliser la relation entre les caractéristiques des billes et les attributs des sciages de
l'érable à sucre (Acer saccharum Marshall) et du bouleau jaune (Betula alleghaniensis
Britton). Nous avons récolté 64 érables à sucre et 32 bouleaux jaunes provenant de deux
endroits au sud du Québec, Canada, qui ont été transformés en billes de sciage, puis en
planches. Au total, 2236 planches ont été classifiées selon les grades et les catégories de
couleurs de la National Hardwood Lumber Association (NHLA). En tenant compte de la
forte proportion de zéros dans les données, nous avons mis au point des modèles statistiques
pour prédire le rendement en volume des différents grades et catégories de couleurs des
sciages. Pour les deux espèces, les grades des planches étaient fortement liés à la longueur
de la bille, à la position de la bille dans l’arbre, au diamètre au fin bout de la bille et au
diamètre de la carie au fin bout de la bille. Pour l'érable à sucre, la couleur des sciages était
liée au volume net de la bille et au volume de la coloration de cœur, tandis que pour le bouleau
jaune, elle était liée à la longueur de la bille, au diamètre au fin bout de la bille et au diamètre
de la coloration de cœur au gros bout de la bille. La capacité prédictive du rendement en
volume de sciage de ces modèles a été supérieure à celle du système de classification des
billes spécifiquement conçu à cette fin. Du point de vue de l’aménagement, la production de
bois de grande valeur devrait se concentrer sur la bille de pied et pourrait être atteinte en
favorisant une croissance radiale rapide de l’arbre afin de limiter le développement de la
coloration de cœur.
62
Introduction
The production of added-value wood products from the North American temperate deciduous
forests is mainly associated with the processing of hardwoods by the appearance wood
products industries. Accordingly, the demand and market value of sugar maple (Acer
saccharum Marshall) and yellow birch (Betula alleghaniensis Britton) trees depend on the
visual characteristics of their manufactured products assortment. Variations in quality
between and within stems imply that logs must be separated into different potential uses
before being supplied to the relevant mill. This can be achieved using tree grading rules
(Hanks 1976; Monger 1991) that were developed to assess stem quality prior to harvest. Like
log grading rules also in use (Rast et al. 1973; Petro and Calvert 1976), these classification
systems aim to predict the potential for lumber production, except that standing tree quality
is based only on an assessment of the butt log.
Fortin et al. (2009b) developed a two-part conditional model to address the issue of predicting
the log grading assortment from an assessment of standing tree quality. In this model, log
grades are based on estimates of the merchantable value of the lumber pieces that can be
extracted from a given sawlog (Petro and Calvert 1976). Lumber value predictions can be
obtained by adjusting the prices of the of the National Hardwood Lumber Association
(NHLA 2011) lumber grades to their current market value. However, such lumber value
estimates are based on a single study, conducted almost four decades ago, that provided little
information about the factors that induce variations in the lumber products assortment, and
thus monetary value among or within log grades.
In practice, the lumber value of sugar maple and yellow birch trees is determined by the
grades and the color of sawn pieces (Hardwood Market Report 2011). Drouin et al. (2010)
found that tree diameter is the most important variable affecting the distribution of NHLA
grades in white birch, while wood color variability was mostly affected by the diameter, age
and vigor of standing trees. Other studies showed the link between the occurrence and size
of red heartwood and the presence of external defects and injuries in standing trees (Shigo
1967; Knoke 2003; Wernsdorfer et al. 2005; Belleville et al. 2011; Baral et al. 2013),
suggesting that lumber color distribution can vary according to the occurrence of defects.
63
Because of this emphasis on quality, a major challenge in northern hardwood forests has been
to supply the appearance wood products industries while avoiding the gradual depletion of
the resources (Erickson et al. 1990; Nyland 1992). In a context where managed forests have
to provide multiple, and sometimes conflicting, services (Leak et al. 2014), it is important to
strive to extract maximum value from each harvested tree. Understanding the factors that
affect lumber assortment in trees and logs can help attain this objective by optimizing the
forest value chain, from designing adequate silvicultural systems to improving wood
procurement and allocation choices (Muñoz et al. 2013; Bennett 2014).
Whereas some studies have investigated in details the composition of the products basket in
white birch (Betula papyrifera Marshall) (Drouin et al. 2010) and in softwoods (Barrette et
al. 2012; Auty et al. 2014), no such work is available, to our knowledge, for sugar maple and
yellow birch. Yet, these two species have considerable economic importance in the North
American wood market, and their monetary value is known to vary considerably with
changes in stem or wood properties (Wiedenbeck et al. 2004; Havreljuk et al. 2014). Even if
tree value was related to log or stem characteristics in these studies, it is not possible to
determine to which extent a change in tree value was caused either by the variation in lumber
volume or lumber grades, or both.
The objective of this study was to investigate the relationship between log characteristics and
sawn board attributes in sugar maple and yellow birch. More specifically, we aimed to
develop models for predicting the occurrence and volume of each NHLA lumber grade in a
given log. From a statistical point of view, the modeling of product assortment from trees or
logs is challenging because of the multiple lumber grades and the excess of “zeros” in the
responses for certain classes of logs or board types. We therefore used generalized additive
models with a beta inflated distribution (Rigby and Stasinopoulos 2009) as a framework to
predict the occurrence and the volume of the various lumber grades that can be produced
from logs of both species.
64
Material and methods
Study area
Two study sites were selected for this study, both located in the temperate forest zone of the
southern Québec, Canada. The first site (S1) was located near Québec City (46°56’ N; 71°40’
W) within the balsam fir (Abies balsamea [L.] Mill.) – yellow birch bioclimatic domain
(Robitaille and Saucier 1998). The sampled stand has a total basal area (BA) of merchantable
standing trees of 23.5 m² ha-1, composed of sugar maple (38%), yellow birch (36%) and
American beech (Fagus grandifolia Ehrh.) (26%). The second site (S2) was located near
Mont-Laurier (46°39’ N; 75°38’ W), within the sugar maple – yellow birch bioclimatic
domain (Robitaille and Saucier 1998). The measured total BA of merchantable standing trees
was 25.0 m² ha-1, and was mainly composed of sugar maple (87%) with minor components
of yellow birch (6%), American beech (5%) and red maple (Acer rubrum L.) (2%). Both sites
were located on moderately to well-drained glacial tills and extend on an area of about 50 ha.
The mean annual temperature and precipitation was estimated at 3.2 °C / 1368 mm and 2.3
°C / 1013 mm for S1 and S2, respectively (Régnière et al. 2012).
Tree selection
At each study site, 32 sugar maple and 16 yellow birch trees were selected for a total of 96
stems. In order to incorporate stem heterogeneity into the sampling, sample trees were
selected according to the wide range of tree vigor and quality classes provided by Boulet
(2007) and Monger (1991), respectively. The tree vigor classification is a four-class system
that aims to identify stems with the highest risk of dying before the next cutting cycle
according to the presence and severity of observable defects on the tree (Boulet 2007). The
tree quality classification characterizes stem potential for producing sawlogs, according to
the stem size and the observable defects on the lower 5 m of the tree (Monger 1991). To be
consistent with the merchantable limit of the hardwoods intended for sawing, the assessments
were limited to stems with a diameter at breast height (DBH, 1.3 m above ground level)
greater than 23 cm.
65
Log classification
Felling operations were conducted in 2009 and 2010 at the Duchesnay and Mont-Laurier
sites, respectively. Full-length trees, including large branches with sawing potential, were
transported to the Duchesnay sawmill (Sainte-Catherine-de-la-Jacques-Cartier, Québec) for
log grading. Log grading was made according to the Petro and Calvert (1976) log grading
rules, which are similar to those used by the US Forest Service (Rast et al. 1973). The factors
considered in log grading include log size (length and small-end diameter), log position along
the bole, number of clear face cuttings (defect-free sections), straightness and soundness of
the log (Hanks et al. 1980). Three grades (F1, F2 and F3) were used to describe sawlog
potential for factory lumber grade products, where the highest quality corresponds to grade
F1 (i.e., Factory-1) and the lowest to grade F3 (i.e., Factory-3). An additional sawlog category
(F4) was included to represent small diameter bolts (Bumgardner et al. 2001). Other low-
grade logs were classified as pulpwood or waste logs. Veneer logs were distinguished
throughout the bucking stage, but these were combined with sawlogs in the analyses because
of their scarce occurrence. Log volume measurements were calculated using Smalian’s
equation (Avery and Burkhart 2001). A summary of the mean log characteristics is presented
in Table 3.1.
Table 3.1 Mean log characteristics for the sugar maple and yellow birch data.
No.
Mean length ±SD
[range] (cm)
Small-end
diameter
±SD (cm)
Large-end
diameter
±SD (cm)
Mean gross
volume ±SD
[range] (dm3)
Mean net volume
±SD [range] (dm3)
Red heartwood
volume ±SD
(dm3)
Sugar maple 123 247 ±72 [128-382] 30 ±5 33 ±7 202 ±109 [46-535] 196 ±106 [46-535] 47 ±36
F1 5 338 ±28 [316-379] 34 ±1 43 ±4 375 ±27 [335-401] 373 ±25 [335-401] 52 ±31
F2 27 319 ±45 [252-382] 34 ±5 39 ±5 332 ±81 [208-535] 325 ±79 [208-534] 70 ±40
F3 49 267 ±28 [245-381] 28 ±5 31 ±5 187 ±62 [82-363] 181 ±56 [82-326] 49 ±36
F4 42 165 ±37 [128-254] 28 ±5 30 ±6 115 ±61 [46-424] 111 ±55 [46-382] 29 ±22
Yellow birch 66 247 ±74 [126-381] 29 ±6 33 ±7 200 ±113 [38-497] 196 ±111 [38-485] 60 ±54
F1 5 326 ±33 [293-381] 38 ±3 43 ±4 412 ±78 [332-497] 403 ±68 [332-485] 143 ±39
F2 17 296 ±44 [253-379] 33 ±3 38 ±5 292 ±66 [191-460] 286 ±64 [188-438] 99 ±62
F3 25 272 ±41 [250-381] 27 ±5 30 ±5 176 ±65 [89-373] 173 ±64 [89-373] 42 ±30
F4 19 148 ±25 [126-194] 27 ±6 28 ±6 94 ±48 [38-198] 90 ±45 [38-196] 28 ±27
Total 189 247 ±73 [126-382] 30 ±6 33 ±7 201 ±110 [38-535] 196 ±197 [38-535] 51 ±44
66
Sawmill conversion
A total of 189 sawlogs were produced throughout the bucking stage. Twelve sugar maple and
four yellow birch trees generated only pulp logs and were discarded from the study. The
majority of sawlogs (128) were processed at the Duchesnay sawmill. Because of their smaller
size, the 61 bolts were sawn using a portable sawmill (Wood-Mizer Products Inc., USA) at
Laval University’s Renewable Materials Research Centre (Quebec City, Canada). The
production of high grade lumber (i.e., knot-free sapwood) was maximized using the grade
sawing approach (Richards et al. 1979), which consists of progressively rotating the log by
90 degrees once the heartwood is reached on one sawn face (Steele 1984). For consistency,
logs from both study sites were sawn by the same qualified workers and the provenance (i.e.,
tree and log) of each board was traced during the conversion process.
Lumber classification
The sawing trial resulted in a total of 2236 lumber pieces with standard 2.54 cm thickness (1
inch) and variable widths and lengths ranging from 7.6 to 35.6 cm (3 to 14 inches ) and 1.22
to 3.62 m (4 to 12 feet), respectively. Sugar maple and yellow birch boards were graded
according to the standards of the National Hardwood Lumber Association (2011). The initial
step in the lumber grading consisted in measuring the number of board feet in each piece.
One board foot (2360 cm³) is the equivalent of a 30.48 cm long x 30.48 cm wide x 2.54 cm
thick (1 foot x 1 foot x 1 inch) board. Standard lumber grades applied to both species were
mainly related to the size of clear face cuttings (i.e., free of defects) and were divided classes
of similar quality (FAS, FAS one face (F1F), Selects, No. 1 Common, No. 2A Common, No.
3A Common and No. 3B Common, with the best grade being FAS and the lowest No. 3B
Common). Boards of a lower grade than No. 3B Common (i.e., pallet lumber) were discarded
from the study. All sawn boards were also assessed for color specifications according to the
NHLA (2011) rules. Color selection for sugar maple and yellow birch is optional, but its
assessment can help specify the end uses and, therefore, the market value of boards.
Depending on the extent of non-discolored wood (wrongly referred to as “sapwood” in the
wood processing industry (Baral et al. 2013)) on the faces and edges of each piece, sugar
maple boards were classified as No. 1 White Maple, No. 2 White Maple or Sap Hard Maple
67
in descending order of quality. In the No. 1 White Maple category, both faces and both edges
of the required cuttings need to be non-discolored, while in the No. 2 White Maple category
the same rules apply except that only one face, both edges and over 50% of the reverse side
of the cuttings should not contain discolored heartwood. The requirements for Sap Hard
Maple were the same as those for the Sap Birch, where a cutting needs to have at least one
non-discolored face. Yellow birch lumber color assessment was also considered for “Red”
birch, where each required cuttings need to have one clear heartwood (i.e., discolored) face.
For both species, lumber pieces not satisfying the NHLA color specifications were classified
as regular wood. For consistency, boards from both sites were graded by the same qualified
inspector. The distribution of sawn lumber is presented in Table 3.2.
Table 3.2 Lumber grade distribution among the sawn boards.
NHLA grades Total no. of boards No. of board feet % of board feet
Sugar maple 1460 5469 100.0
FAS 61 372 6.8
F1F 61 370 6.8
Selects 98 348 6.4
No. 1C 265 1029 18.8
No. 2A 324 1160 21.2
No. 3A 252 850 15.5
No. 3B 399 1340 24.5
Yellow birch 776 2989 100.0
FAS 51 307 10.3
F1F 39 214 7.2
Selects 61 239 8.0
No. 1C 182 731 24.5
No. 2A 178 609 20.4
No. 3A 120 397 13.3
No. 3B 145 492 16.5
Statistical approach
The response variable of the statistical model was the lumber volume recovery calculated as
the ratio of the volume of each lumber grade over the total net volume of the log. For the
sake of clarity, we will use “VRG” and “VRC” when referring to the lumber volume recovery
of the various board grades and board colors, respectively. Prior to the calculation of lumber
volume recovery, the lumber grade volume represented in board feet was replaced by its
metric equivalent (1 board feet = 0.0023597 cubic meter [m³]) to obtain a ratio of cubic
68
meters of sawn wood divided by a number of cubic meters of roundwood. Therefore, both
VRG and VRC are continuous variables with values theoretically bound between 0 and 1. In
practice, there were no occurrences of 1, but there were many zero values for certain classes
of boards (Figure 3.1 and Figure 3.2).
Figure 3.1 Observed (bars) versus predicted (points) frequencies of the lumber volume
recovery of lumber grades (VRG).
69
Figure 3.2 Observed (bars) versus predicted (points) frequencies of the lumber volume
recovery of the lumber colors (VRC).
This abundance of zeros is caused by the more restrictive criteria for better grades. In our
study, we used generalized additive models (Hastie and Tibshirani 1986) to predict the
product assortment from a given log. The modeling of the mean part and the excess of zeros
of the dependent variable was assessed simultaneously using the beta inflated distribution
with abundance of zeros (BEINF0) implemented in the GAMLSS package (Rigby and
Stasinopoulos 2009) of the R statistical programing environment (R Development Core
Team 2014). The beta distribution is very flexible for modeling data that are measured in a
continuous scale on the open interval (0, 1) since its density can take different shapes
depending on the values of the two parameters that index the distribution (Ospina and Ferrari
2010). The probability function of the zero-inflated beta distribution, denoted by BEINF0
(𝜇, 𝜎, 𝑣) is defined by Eq. 1:
70
(1) 𝑓𝑌(𝑦|𝜇, 𝜎, 𝑣) = {𝑝0 if 𝑦 = 0
(1 − 𝑝0)1
𝐵(𝛼,𝛽)𝑦𝛼−1(1 − 𝑦)𝛽−1 if 0 < y < 1
for 0 ≤ 𝑦 < 1, where
(1.1) 𝛼 = 𝜇(1 − 𝜎2)/𝜎²
(1.2) 𝛽 = (1 − 𝜇)(1 − 𝜎2)/𝜎²
(1.3) 𝑝0 = 𝑣(1 + 𝑣)−1
So, 𝛼 > 0, 𝛽 > 0, 0 < 𝑝0 < 1
Hence BEINF0 (𝜇, 𝜎, 𝑣) has parameters
(1.4) 𝜇 = 𝛼/(𝛼 + 𝛽)
(1.5) 𝜎 = (𝛼 + 𝛽 + 1)−1/2
(1.6) 𝑣 = 𝑝0/1 − 𝑝0
So, 0 < 𝜇 < 1, 0 < 𝜎 < 1, 𝑣 > 0
(1.7) 𝐸(𝑦) =𝜇
(1+𝑣)
The three parameters 𝜇 (mean), 𝜎 (dispersion) and 𝑣 (probability of zero) were each modelled
using the independent explanatory variables. To respect the parameter hierarchy when fitting
the model (Rigby and Stasinopoulos 2009), the 𝜇 parameter was fitted before the 𝜎
parameter. The explanatory variables were allowed to differ for each part of the model (i.e.,
beta and probability of zero).
Model selection
Prior to fitting, we made several hypotheses about the variables that could have an effect on
the fit of each part of the model. Log grade and log length were expected to have a strong
effect on the abundance of zeros in the model because the valuable lumber grades are
characterized by longer and larger pieces, which are not present in bolts and lower log grades.
For example, the minimum board size for lumber grades FAS and F1F is 15 cm (6 inch) wide
71
by 2.5 m (8 feet) long so that the probability for low log grades to produce such a lumber
piece is low. Lumber grades and colors were considered separately in order to limit the
number of potential combinations of product assortments. For the lumber grade models, we
tested the interaction between NHLA lumber grades and the two species studied, while
separate models were calibrated for color specifications to reflect the fact that, in this case,
the grading specifications varied between species.
Prior to model selection, all variables were tested individually according to their relationship
with lumber grades and colors. This step allowed to discriminate the most important variables
to be included in the model selection process. Then, the main independent variables included
in the modeling of the different parameters of the BEINF0 distribution were subsequently
eliminated through a backward elimination procedure. The corrected Akaike information
criterion (AICc) (Burnham and Anderson 2002) was used to determine if the contribution of
a variable to the model fit was significant or not. The AICc was preferred to the AIC statistic
(Akaike 1974) because it is more appropriate for small samples and includes a greater penalty
for extra parameters (Anderson 2008). Models with the lowest AICc were preferred. Models
were compared to the intercept-only model, specified for each part. In total, 1323
observations were used for the model fitting of the VRG (i.e., 189 logs x 7 lumber grades),
while 492 (i.e., 123 logs x 4 lumber colors) and 198 observations (i.e., 66 logs x 3 lumber
colors) were used for the sugar maple and yellow birch VRC, respectively. The goodness-of-
fit of each model was assessed by checking the independence of residuals on the response
variable and the residual normality, as described by Stasinopoulos and Rigby (2007). Fit
indices (pseudo-R²) were also calculated for each model, but these were not used as a criterion
for model selection. In addition, to present the general performance of the best model in a
straightforward manner, the predictions for each board grade were converted to their
monetary value (Hardwood Market Report 2008–2012) (Table 3.3), before being summed
per log grade.
72
Table 3.3 Mean sugar maple and yellow birch lumber values from 2008 to 2012.
NHLA grades Hard maple Birch
Regular Sap No. 1&2 White Regular Red Sap
FAS 1195 1295 1420 1105 1410 1380
Selects 1175 1275 1400 1085 1390 1360
No. 1C 760 860 860 685 990 960
No. 2A 540 640 640 430 735 705
No. 3A 355 455 – 280 585 555
No. 3B (pallet) 225 – – 225 – –
Note: Values are presented in US$ per MBF for 2.54 cm thick (1 inch) boards of random widths and lengths
that are rough and green. 1000 board feet (MBF) = 2.36 m³.
73
Results
Lumber grade models
The volume proportion of the best lumber grades (No. 1C and Better) was 59.5%, 49.8% and
30.6% for sugar maple log grades F1, F2 and F3, respectively. For yellow birch, the
corresponding values were 67.9%, 60.6% and 34.9% (Table 3.4).
Table 3.4 Proportion of NHLA lumber grades and colors among log grades.
Lumber grades proportion (%) Color specifications proportion (%)
FAS F1F Selects No.
1C
No.
2A
No.
3A
No.
3B
No. 1
White
No. 2
White Sap Red Regular
Sugar maple 6.8 6.8 6.4 18.8 21.2 15.5 24.5 18.5 10.1 14.8 – 51.9
F1 17.3 15.6 7.8 18.8 17.6 5.8 17.1 26.1 16.1 11.3 – 46.5
F2 12.8 11.1 6.5 19.4 21 10.9 18.4 22.4 14.1 12.1 – 51.4
F3 1.9 3.8 6.7 18.2 21.1 20.2 28.1 13.5 7.2 16.5 – 62.8
F4 0 0 4.8 18.8 23.6 19.8 33.1 17.7 4.8 18.5 – 59.1
Yellow birch 10.3 7.2 8.0 24.5 20.4 13.3 16.5 – – 37.9 10.3 51.9
F1 22 13 7.2 25.7 13.2 7 11.9 – – 31.7 16.3 52.1
F2 14.1 9.4 7.6 29.5 17.9 10.1 11.6 – – 37.6 13.5 48.9
F3 3.5 4.1 9.6 17.7 26.5 19 19.6 – – 41.7 4.7 53.6
F4 0 0 5.6 25.3 21.2 16.6 31.2 – – 35.9 7.2 56.9
Even if the overall proportion of the best lumber grades was higher for each log grade in
yellow birch logs than in sugar maple, both species were considered together in the VRG
model because the goodness of fit was not significantly improved by the inclusion of
interactions between species and other covariates. The list of models tested is presented in
Table 3.5.
The best model predicting VRG was model 8 (AICc = -1523.1), followed by model 9 (AICc
= -1503.1, ∆i =20.0), which contained more variables, suggesting that the inclusion of
additional covariates, such as the number of clear wood faces, did not substantially improve
the model fit (Table 3.5). The probability of zero occurrence (𝑣) and the mean (𝜇) were
explained by a slightly different list of covariates. The occurrence of zeros was mostly
explained by the small-end diameter of the log, log length and log position, while the main
74
variables related to the mean were the small-end diameter of the log, log position and the
decay diameter at the small-end of the log.
Table 3.5 List of models predicting the VRG of sugar maple and yellow birch.
Model group ID Part Explanatory variables
Individual
components Complete model
AICc R² d.f. LL AICc ∆i R²
Intercept 0 . Null . . 3 277.9 -549.9 973.2 0.00
Mean 1
µ Grade -614.3 0.06
21 593.9 -1145.0 378.1 0.38 σ Grade -539.6 0.00
ν Grade -1073.2 0.33
Log grading
classification 2
µ Grade x Petro -650.6 0.11
82 790.1 -1405.3 117.8 0.54 σ Grade x Petro -536.9 0.03
ν Grade x Petro -1296.5 0.45
Volumetric
covariates
3
µ Grade x Net volume -698.6 0.12
42 779.5 -1472.1 51.0 0.53 σ Grade x Net volume -565.3 0.03
ν Grade x Net volume -1305.6 0.45
4
µ Grade x Net volume + Grade x Decay volume -704.7 0.14
77 830.0 -1496.4 26.7 0.57 σ Grade x Net volume -565.3 0.03
ν Grade x Net volume + Grade x Clear faces -1326.4 0.48
Other log
measurements
5
µ Grade x Small-end diameter -701.7 0.13
42 738.7 -1390.6 132.5 0.50 σ Grade x Small-end diameter -564.5 0.03
ν Garde x Small-end diameter -1226.7 0.41
6
µ Grade x Length -628.0 0.08
42 678.6 -1270.4 252.7 0.45 σ Grade x Length -546.1 0.02
ν Grade x Length -1185.6 0.39
7
µ Grade x Small-end diameter + Grade x Length -700.1 0.13
56 791.5 -1466.0 57.1 0.54 σ Grade x Small-end diameter -564.5 0.03
ν Grade x Small-end diameter + Grade x Length -1299.6 0.45
8
µ Grade x Small-end diameter + Grade x Position
+ Grade x Small-end decay -722.8 0.16
70 835.5 -1523.1 0.0 0.57 σ Grade x Small-end diameter -564.5 0.03
ν Grade x Small-end diameter + Grade x Position + Grade x Length
-1331.7 0.47
9
µ Grade x Small-end diameter + Grade x Position + Grade x Small-end decay + Clear faces
-708.4 0.19
125 889.7 -1503.1 20.0 0.60 σ Grade x Small-end diameter -564.5 0.03
ν Grade x Small-end diameter + Grade x Position
+ Grade x Length + Clear faces -1333.9 0.49
Full model 10
µ
Grade x (Region + Species + Small-end
diameter + Length + Position + Small-end
decay + Clear faces)
-702.6 0.21
167 940.4 -1498.2 24.9 0.63 σ Grade x Species -531.3 0.00
ν
Grade x (Region + Species + Small-end
diameter + Length + Position + Small-end
decay + Clear faces)
-1334.0 0.51
Note: d.f. is the degrees of freedom, LL is the Log-Likelihood, ∆i is the difference in the AICc and that of the
best model and R² is pseudo-R². The fit indices for individual components of the model are presented for
illustrative purposes only and were not used for the model fitting.
75
The most important variations in VRG for all covariates were observed with the lowest lumber
grade (No. 3B) and the best lumber grades (FAS and F1F). An important decrease in the VRG
of No. 3B with increasing log length was compensated by an increase in the VRG of the best
lumber grades, around 2.50 and 3.50 m (Figure 3.3). Similarly, the VRG of the lowest lumber
grades decreased with an increase of the small-end diameter of the log and was exceeded by
the VRG of the best lumber grades at a diameter of about 38 cm (Figure 3.3). Higher
proportions of VRG for the FAS, F1F and Selects were observed with logs that originated
from the bottom part of the tree. Conversely, the VRG of No. 3A and No. 3B grades increased
in the upper logs. No clear trend was observed between VRG and the decay diameter at the
small-end of the log even if the overall lumber volume recovery was higher for the lowest
lumber grades (Figure 3.3). Throughout the model calibration process, the zero-part (𝑣) was
more sensitive to the addition of variables as these brought larger increases to the overall
model fit (Table 3.5). Parameter estimates for the best model predicting VRG are presented
in Table 3.6.
Figure 3.3 Predicted lumber volume recovery for each lumber grade (VRG) plotted against
the small-end diameter of the log (cm) of the best model (model 8). Lines represent loess
smoothing functions with standard error through the predictions.
76
Table 3.6 Parameter estimates (and standard errors) for the best model to predicting VRG (model 8).
Model part : Mean (µ)
Board grade Intercept Grade Position Small-end diameter Decay diameter Grade x Position Grade x Small-end
diameter
Grade x Decay
diameter
FAS -3.3999 (0.8134) 0 -0.0009 (0.0006) 0.0439 (0.0248) -0.0332 (0.0251) 0 0 0
F1F -3.3999 (0.8134) -0.0670 (0.9911) -0.0009 (0.0006) 0.0439 (0.0248) -0.0332 (0.0251) 0.0014 (0.0007) -0.0164 (0.0301) 0.0658 (0.0321)
Selects -3.3999 (0.8134) 1.5013 (0.9168) -0.0009 (0.0006) 0.0439 (0.0248) -0.0332 (0.0251) 0.0004 (0.0007) -0.0607 (0.0283) 0.0369 (0.0301)
No. 1C -3.3999 (0.8134) 0.8111 (0.8889) -0.0009 (0.0006) 0.0439 (0.0248) -0.0332 (0.0251) 0.0008 (0.0007) -0.0249 (0.0273) 0.0467 (0.0285)
No. 2A -3.3999 (0.8134) 1.5286 (0.8685) -0.0009 (0.0006) 0.0439 (0.0248) -0.0332 (0.0251) 0.0010 (0.0007) -0.0488 (0.0266) 0.0308 (0.0281)
No. 3A -3.3999 (0.8134) 2.2931 (0.8702) -0.0009 (0.0006) 0.0439 (0.0248) -0.0332 (0.0251) 0.0015 (0.0007) -0.0855 (0.0267) 0.0262 (0.0279)
No. 3B -3.3999 (0.8134) 3.4951 (0.8435) -0.0009 (0.0006) 0.0439 (0.0248) -0.0332 (0.0251) 0.0013 (0.0006) -0.1164 (0.0258) 0.0851 (0.0265)
Model part : Dispersion (σ)
Board grade Intercept Grade Small-end diameter Grade x Small-end diameter
FAS -3.9118 (1.3326) 0 0.0750 (0.0393) 0
F1F -3.9118 (1.3326) 0.8891 (1.7790) 0.0750 (0.0393) -0.0376 (0.0526)
Selects -3.9118 (1.3326) 1.59122 (1.5232) 0.0750 (0.0393) -0.0542 (0.0457)
No. 1C -3.9118 (1.3326) 2.1067 (1.4139) 0.0750 (0.0393) -0.0576 (0.0422)
No. 2A -3.9118 (1.3326) 2.3989 (1.3813) 0.0750 (0.0393) -0.0670 (0.0411)
No. 3A -3.9118 (1.3326) 3.0668 (1.4112) 0.0750 (0.0393) -0.0969 (0.0422)
No. 3B -3.9118 (1.3326) 3.1503 (1.3660) 0.0750 (0.0393) -0.0104 (0.0405)
Model part : Probability of zero (ν)
Board grade Intercept Grade Length Position Small-end diameter Grade x Length Grade x Position Grade x Small-end diameter
FAS 10.1162 (1.9744) 0 -0.0115 (0.0037) 0.0045 (0.0013) -0.2145 (0.0512) 0 0 0
F1F 10.1162 (1.9744) 2.0545 (2.8324) -0.0115 (0.0037) 0.0045 (0.0013) -0.2145 (0.0512) -0.0071 (0.0054) -0.0026 (0.0016) -0.0037 (0.0707)
Selects 10.1162 (1.9744) -6.1606 (2.3210) -0.0115 (0.0037) 0.0045 (0.0013) -0.2145 (0.0512) 0.0041 (0.0045) -0.0016 (0.0015) 0.1299 (0.0613)
No. 1C 10.1162 (1.9744) -5.8310 (2.5571) -0.0115 (0.0037) 0.0045 (0.0013) -0.2145 (0.0512) 0.0134 (0.0051) -0.0028 (0.0015) -0.0427 (0.0745)
No. 2A 10.1162 (1.9744) -6.7677 (2.9493) -0.0115 (0.0037) 0.0045 (0.0013) -0.2145 (0.0512) 0.0056 (0.0062) -0.0028 (0.0016) 0.0134 (0.0865)
No. 3A 10.1162 (1.9744) -7.9821 (2.4636) -0.0115 (0.0037) 0.0045 (0.0013) -0.2145 (0.0512) 0.0044 (0.0049) -0.0061 (0.0015) 0.1493 (0.0671)
No. 3B 10.1162 (1.9744) -12.9144 (2.8608) -0.0115 (0.0037) 0.0045 (0.0013) -0.2145 (0.0512) 0.0188 (0.0059) -0.0049 (0.0017) 0.1593 (0.0765)
77
Lumber color models
For sugar maple, the proportion of non-discolored wood (No. 1 White Maple, No. 2 White
Maple and Sap Hard Maple) was greater for logs of highest quality (Table 3.4). For yellow
birch, the proportion of Sap Birch was constant through the log grades, while a decreasing
trend was observed from F1 to F4 for the Red Birch category (Table 3.4). Details of the
model fitting process for sugar maple and yellow birch are presented in Table 3.7 and Table
3.8, respectively.
The main variables related to VRC in the best sugar maple model (model 4, AICc = -736.7)
were the net volume of the log and the volume of red heartwood. The inclusion of clear wood
faces and decay volume did not improve the fit of the second best model (model 5, ∆i = 7.4).
Other models including other log measurements gave lower fit than log volume. The VRC of
No. 1 and No. 2 White Maple color specifications increased with the log net volume, while
it decreased for Sap Hard Maple. A non-significant change was observed in the VRC for the
regular color category. Conversely, the VRC of the regular lumber category increased with
the red heartwood volume of the log, while a decreasing trend was observed for the No.1
White Maple and Sap Hard Maple (Figure 3.4).
Contrary to the VRC model for sugar maple, which was related to volumetric covariates, the
most important variables for yellow birch were related to other log measurements. The best
model for predicting the VRC in this species was model 9 (AICc = -311.7), followed by model
10 (AICc = -306.6, ∆i = 5.1) that contained some additional variables. The main covariates
associated with the mean volume recovery (𝜇) of a given color grade were the small-end
diameter of the log, log length and the large-end diameter of heartwood, while the occurrence
of zeros (𝑣) was related to the large-end diameter of heartwood. No clear trends in VRC of
Sap Birch and regular lumber were found against log length and the small-end diameter of
the log, but the VRC of the Red Birch category tended to increase with an increase of the log
dimensions (Figure 3.5). In addition, for logs with a large-end diameter of red heartwood
over 16 cm, the proportion of the Regular wood and Red Birch categories increased, while
Sap Birch decreased (Figure 3.5). Parameter estimates for the best model to predicting VRC
of sugar maple and yellow birch are presented in Table 3.9.
78
Table 3.7 List of models predicting the VRC of sugar maple.
Model group ID Part Explanatory variables
Individual
components Complete model
AICc R² d.f. LL AICc ∆i R²
Intercept 0 . Null . . 3 109.2 -212.3 524.4 0.00
Mean 1
µ Color -502.3 0.45
12 317.1 -609.5 127.2 0.45 σ Color -225.6 0.04
ν Color -303.6 0.18
Log grading
classification 2
µ Color -502.3 0.45
24 339.5 -628.5 108.2 0.61 σ Color -225.6 0.04
ν Color x Petro -323.2 0.25
Volumetric covariates
3
µ Color x Net volume -502.7 0.46
20 341.5 -641.1 95.6 0.61 σ Color -225.6 0.04
ν Color x Net volume -331.2 0.24
4
µ Color x Net volume + Color x Red heartwood volume -592.3 0.56
28 398.1 -736.7 0.0 0.69 σ Color -225.6 0.04
ν Color x Net volume + Color x Red heartwood volume -355.4 0.30
5
µ Color x Net volume + Color x Red heartwood volume
+ Color x Decay volume + Color x Clear faces -585.7 0.57
36 403.6 -729.3 7.4 0.70 σ Color -225.6 0.04
ν Color x Net volume + Color x Red heartwood volume -355.4 0.30
Other log measurements
6
µ Color x Large-end red heartwood diameter -550.2 0.51
20 349.0 -656.2 80.5 0.62 σ Color -225.6 0.04
ν Color x Small-end red heartwood diameter -313.4 0.21
7
µ Color x Length -500.8 0.46
20 328.9 -616.1 120.6 0.59 σ Color -225.6 0.04
ν Color x Length -311.5 0.21
8
µ Color -502.3 0.45
16 335.0 -636.9 99.8 0.60 σ Color -225.6 0.04
ν Color x Small-end diameter -331.2 0.24
9
µ Color x Large-end red heartwood diameter -550.2 0.51
28 384.7 -709.3 27.4 0.67 σ Color -225.6 0.04
ν Color x Small-end red heartwood diameter + Color x Small-end diameter + Color x Length
-367.8 0.32
10
µ Color x Large-end red heartwood diameter + Color x
Clear faces + Color x Position -556.2 0.53
36 396.4 -715.0 21.7 0.69 σ Color -225.6 0.04
ν Color x Small-end red heartwood diameter + Color x
Small-end diameter + Color x Length -367.8 0.32
Full model 11
µ
Color x (Small-end diameter + Large-end red
heartwood diameter + Large-end decay + Length +
Position + Clear faces)
-578.0 0.58
60 421.5 -706.0 30.7 0.72 σ Color -225.6 0.04
ν
Color x (Small-end diameter + Small-end red
heartwood diameter + Large-end decay + Length + Position + Clear faces)
-346.0 0.32
Note: d.f. is the degrees of freedom, LL is the Log-Likelihood, ∆i is the difference in the AICc and that of the
best model and R² is pseudo-R². The fit indices for individual components of the model are presented for
illustrative purposes only and were not used for the model fitting.
79
Table 3.8 List of models predicting the VRC of yellow birch.
Model group ID Part Explanatory variables
Individual
components Complete model
AICc R² d.f. LL AICc ∆i R²
Intercept 0 . Null . . 3 18.2 -30.2 281.5 0.00
Mean 1
µ Color -75.9 0.22
9 108.4 -197.8 113.9 0.60 σ Color -43.5 0.08
ν Color -144.1 0.45
Log grading classification
2
µ Color -75.9 0.22
18 118.1 -196.3 115.4 0.64 σ Color -43.5 0.08
ν Color x Petro -143.5 0.50
Volumetric
covariates
3
µ Color -75.9 0.22
12 124.4 -223.0 88.7 0.66 σ Color -43.5 0.08
ν Color x Net volume -169.6 0.53
4
µ Color x Net volume + Color x Red heartwood volume -138.8 0.47
18 166.8 -293.8 17.9 0.78 σ Color -43.5 0.08
ν Color x Red heartwood volume -186.7 0.57
5
µ Color x Net volume + Color x Red heartwood volume
+ Color x Clear faces -135.5 0.48
24 169.0 -283.0 28.7 0.78 σ Color -43.5 0.08
ν Color x Red heartwood volume + Color x Clear faces -180.1 0.57
Other log
measurements
6
µ Color x Large-end red heartwood diameter -101.4 0.34
15 149.7 -266.8 44.9 0.74 σ Color -43.5 0.08
ν Color x Large-end red heartwood diameter -189.4 0.58
7
µ Color x Length -74.3 0.24
15 114.7 -196.7 115.0 0.62 σ Color -43.5 0.08
ν Color x Length -143.9 0.47
8
µ Color x Small-end diameter -75.9 0.22
15 130.3 -227.9 83.8 0.68 σ Color -43.5 0.08
ν Color x Small-end diameter -179.5 0.55
9
µ Color x Length + Color x Small-end diameter + Color
x Large-end red heartwood diameter -155.8 0.53
21 179.5 -311.7 0.0 0.80 σ Color -43.5 0.08
ν Color x Large-end red heartwood diameter -189.4 0.58
10
µ
Color x Length + Color x Small-end diameter + Color
x Large-end red heartwood diameter + Color x Small-
end red heartwood diameter
-158.9 0.55
27 184.7 -306.6 5.1 0.81 σ Color -43.5 0.08
ν Color x Large-end red heartwood diameter + Color x
Small-end red heartwood diameter -183.6 0.58
Full model 11
µ
Color x (Small-end diameter + Large-end red
heartwood diameter + Large-end decay + Length +
Position + Clear faces)
-149.2 0.57
45 189.3 -261.3 50.4 0.82 σ Color -43.5 0.08
ν
Color x (Small-end diameter + Large-end red
heartwood diameter + Large-end decay + Length +
Position + Clear faces)
-157.5 0.58
Note: d.f. is the degrees of freedom, LL is the Log-Likelihood, ∆i is the difference in the AICc and that of the
best model and R² is pseudo-R². The fit indices for individual components of the model are presented for
illustrative purposes only and were not used for the model fitting.
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Figure 3.4 Predicted lumber volume recovery for each color category (VRC) plotted against the covariates of the best model for sugar
maple (model 4). Lines represent loess smoothing functions with standard error through the predictions.
Figure 3.5 Predicted lumber volume recovery for each color category (VRC) plotted against the covariates of the best model for yellow
birch (model 9). Lines represent loess smoothing functions with standard error through the predictions.
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Table 3.9 Parameter estimates (and standard errors) for the best model to predicting VRC of sugar maple (model 4) and yellow birch
(model 9).
Model part : Mean (µ) for sugar maple
Board color Intercept Color Log net volume Red heartwood volume
Color x Log net volume Color x Red heartwood volume
No. 1 White Maple -2.0745 (0.1421) 0 0.0028 (0.0008) -0.0137 (0.0029) 0 0
No. 2 White Maple -2.0745 (0.1421) -0.6179 (0.2255) 0.0028 (0.0008) -0.0137 (0.0029) -0.0013 (0.0011) 0.0106 (0.0038)
Sap Hard Maple -2.0745 (0.1421) 0.2168 (0.1836) 0.0028 (0.0008) -0.0137 (0.0029) -0.0044 (0.0010) 0.0130 (0.0038)
Regular -2.0745 (0.1421) 1.1010 (0.1641) 0.0028 (0.0008) -0.0137 (0.0029) -0.0052 (0.0009) 0.0259 (0.0032)
Model part : Dispersion (σ) for sugar maple
Board color Intercept Color
No. 1 White Maple -1.2749 (0.0814) 0
No. 2 White Maple -1.2749 (0.0814) -0.3968 (0.1245)
Sap Hard Maple -1.2749 (0.0814) -0.2549 (0.1117)
Regular -1.2749 (0.0814) -0.1386 (0.1102)
Model part : Probability of zero (ν) for sugar maple
Board color Intercept Color Log net volume Red heartwood
volume Color x Log net volume
Color x Red heartwood
volume
No. 1 White Maple 0.56874 (0.6147) 0 -0.0271 (0.0070) 0.0561 (0.0155) 0 0
No. 2 White Maple 0.56874 (0.6147) 1.1488 (0.7240) -0.0271 (0.0070) 0.0561 (0.0155) 0.0158 (0.0070) -0.0523 (0.0174)
Sap Hard Maple 0.56874 (0.6147) -3.2628 (0.8821) -0.0271 (0.0070) 0.0561 (0.0155) 0.0234 (0.0080) -0.0278 (0.0188)
Regular 0.56874 (0.6147) -20.1978 (2124) -0.0271 (0.0070) 0.0561 (0.0155) 0.0271 (12.400) -0.0561 (36.50)
Model part : Mean (µ) for yellow birch
Board color Intercept Color Length Small-end diameter Red heartwood
diameter Color x Length
Color x Small-
end diameter
Color x Red
heartwood diameter
Sap Birch -0.5259 (0.3047) -2.4303 (0.4911) 0.0013 (0.0007) 0.0685 (0.0149) 0.0738 (0.0140) 0.0019 (0.0011) 0.1836 (0.0243) -0.2321 (0.0240)
Red Birch -0.5259 (0.3047) -2.5941 (0.9847) 0.0013 (0.0007) 0.0685 (0.0149) 0.0738 (0.0140) 0.0030 (0.0021) 0.0636 (0.0328) -0.0049 (0.0279)
Regular -0.5259 (0.3047) 0 0.0013 (0.0007) 0.0685 (0.0149) 0.0738 (0.0140) 0 0 0
Model part : Dispersion (σ) for yellow birch
Board color Intercept Color
Sap Birch -1.5412 (0.1002) 0.1589 (0.1418)
Red Birch -1.5412 (0.1002) -0.1763 (0.1887)
Regular -1.5412 (0.1002) 0
Model part : Probability of zero (ν) for yellow birch
Board color Intercept Color Red heartwood diameter Color x Red heartwood diameter
Sap Birch -18.63 (2289) -0.0000 (3237) 29.330 (2289) 0.0000 (129.4)
Red Birch -18.63 (2289) -0.0000 (3237) 29.330 (2289) 0.0000 (183.1) Regular -18.63 (2289) 0 0 0
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Log grading classification
Model comparison confirmed that log grades could be used to predict the lumber grades
assortment (Model 2, AICc = -1405.3), but better results were achieved when log net volume
or other log measurements were used as covariates (Table 3.5). The model considering only
the small-end diameter of the log and log length (Model 7, AICc = -1466.0) was comparable
to the model using only the net volume of the log (Model 3, AICc = -1472.1).
Better predictions of VRC for sugar maple could be achieved by including log grades (Model
2, AICc = -628.5) in the mean model (Model 1, AICc = -609.5), even if the overall fit
remained low (Table 3.7). Conversely, no improvement in AICc was observed when the log
grades (model 2, AICc = -196.3) were added to the yellow birch model (model 1, AICc = -
197.8), suggesting that log grading was not related to the VRC of this species (Table 3.8).
Model evaluation
Observed and predicted frequencies of the volume recovery for each lumber category are
presented in Figure 3.1 and Figure 3.2 for grades and colors, respectively. The overabundance
of zeros justified the use of the zero-inflated beta distribution (BEINF0). Even if the
distribution of the predicted values was satisfactory when compared to the observations for
the grades or color classes that have an overabundance of zeros (FAS, F1F, Red Birch), the
predicted distribution was poor for the grades (No. 1C, No. 2C, No. 3A) and colors (No. 1
White Maple, Sap Hard Maple). However, the overall sum of predictions for each grade or
color class was close to the observed values. Value predictions fitted well the observed data,
although log value was slightly overestimated for the F4 log grade (Figure 3.6). This bias
was probably due to the limited range of net volumes for these small logs and the distribution
problems described earlier.
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Figure 3.6 Predicted value recovery against log net volume established from the predicted
VRG (model 8). Lines represent linear smoothing functions with standard error plotted
against the observed value recovery.
Discussion
Modeling the log (Buongiorno et al. 1993; Fortin et al. 2009b; Rankovic et al. 2013) or
lumber (Lyhykäinen et al. 2009; Drouin et al. 2010; Auty et al. 2014) products assortments
is important to estimate the monetary value of a given tree or forest stand, which are known
to change over time as lumber prices fluctuate (Erickson et al. 1990). In the current study,
we developed a set of models for predicting the lumber yields for grades and colors of sugar
maple and yellow birch from external log characteristics. The volume proportion of the
various lumber grades was similar to those obtained in other similar studies on northern
hardwoods (Petro and Calvert 1976; Hanks et al. 1980; Wengert and Meyer 1994). In the
study of Hanks et al. (1980), nearly 20 000 logs were sawn throughout the Eastern United
States and F1 logs were predicted to yield 60% or more of No. 1C and Better lumber, whereas
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it was 40 to 60% for F2 logs, and less than 40 % for F3 logs. In our study, all volume
proportions were in the same ranges, except the F2 log grade for yellow birch, which was
slightly higher.
The main covariates related to the best lumber grade model (Model 8, Table 3.5) were the
log length, the position of the log in the stem, the small-end diameter of the log and the
diameter of decay at the small-end of the log. As expected, the small-end diameter of the log
and the log length were closely related to the board size minima for a given lumber grade
(NHLA 2011). Similarly, Muñoz et al. (2013) found that the diameter over bark at the small
end of the log was the best predictor of structural sawn lumber in oak (Quercus robur L.).
Log position along the bole could be an indirect indicator of internal wood characteristics
(Petro 1971; Hanks 1976). The butt log is generally considered as the most valuable part of
the tree (Fortin et al. 2009b), as it is larger and more likely to contain a section free of defects
such as knots. This was the case in our study, as more high-grade lumber was found in the
butt logs. Conversely, decay is often associated with volume loss and quality depletion in
standing trees (Basham 1991). Havreljuk et al. (2014) found that visible evidence of fungal
infections and cracks had a negative influence on the value of sugar maple and yellow birch
trees. In the current study, the decay diameter at the small-end of the log had only a limited
effect on the lumber grades assortment. However, the range of decay values was limited, as
many logs with large extent of decay were considered as pulp logs and were discarded from
sawing. Among the other variables that were estimated in the log grading process, the number
of clear face cuttings did not improve the predictions of the VRG. This result is surprising
because this variable is deemed to be an indicator of defects inside the log and, consequently,
of clear face cuttings in the sawn boards. High quality logs are hence characterized by longer
defect-free areas (i.e., clear face cuttings). It is probable that the grouping of all external
defects (i.e., knots, deformations, etc.) in a four-class variable to represent the number of
clear face cuttings on the log resulted in a loss of precision that would explain the lack of
relationship with lumber grades.
The investigation of the relationship between VRG and the log characteristics showed that
the most valuable lumber grades were found at the bottom of the tree, in logs longer than 2.5
m and with a minimum diameter at the small-end above 30 cm. This result is consistent with
85
the specifications of the best log grades in the log classification systems (Hanks 1976; Petro
and Calvert 1976). With the exception of the log position in the stem, the variables included
in the best VRG model can be easily measured and are derived from a log grading system,
such as Petro and Calvert’s (1976). Simplicity is an important advantage of a model based
on a limited number of classes. Although Petro and Calvert’s (1976) log grading system
proved useful to discriminate the VRG between log categories (Figure 3.6) and provided good
predictions with a pseudo-R² of 0.54, the log grading model (Model 2, Table 3.5) was not as
good as model 8, which was based on precise log measurements. The model presented in this
study permitted to quantify to which extent each log characteristic is related to the VRG. As
a result, the curves corresponding to the effect of single log measurements on the VRG for a
given lumber grade may be used to establish some thresholds related to log production
objectives.
In this study, we also presented several models for predicting the assortment of lumber colors.
To our knowledge, this is the first study that describes the relationship between log
characteristics and volume recovery of the various color specifications contained in the
NHLA lumber grading system. In log grading systems (Hanks 1976; Petro and Calvert 1976;
MRNFQ 2011), the red heartwood is only considered when the discolored wood begins to
show some signs of decay, or when it is associated with decayed wood. As a result, some
logs could be downgraded or rejected. Considerations of the diameter of the red heartwood
column at the log cross sections could improve the lumber product assortment, because its
size was found to be positively related to the proportion of the regular lumber for sugar maple
and to the proportion of the regular and “Red Birch” lumber for yellow birch.
Although this study was conducted on the logs and product assortment, the findings may
provide useful guidance for the management of sugar maple and yellow birch in northern
hardwood stands. For a given volume of round wood, our results suggest that forest managers
should aim to produce larger sawlogs, because a higher proportion of the valuable lumber,
both in grades and in colors, was positively related to the log dimensions. However, sawn
timber volume or value in these species is known to decrease beyond DBH thresholds varying
between 40 and 70 cm (Hansen and Nyland 1987; Majcen et al. 1990; Prestemon 1998;
Pothier et al. 2013; Saucier et al. 2014). The accurate assessment of large trees with tree
86
grading systems (Rast et al. 1973; Monger 1991) could be difficult, because of the presence
of some internal defects (Havreljuk et al. 2014). Even if no direct relationship was established
in this study between defect-free sections and lumber volume recovery, the production of
defect-free boles remains desirable as it could limit the proportion of red heartwood in a tree
(Giroud et al. 2008; Belleville et al. 2011; Baral et al. 2013; Havreljuk et al. 2013).
From a modeling point of view, the models for predicting the lumber yields presented in this
study could replace the old yield tables of Petro and Calvert (1976). The estimates of volume
recovery for the F4 logs are also a new contribution that could be implemented in growth
simulators (Fortin et al. 2009a). Theoretically, it would be possible to predict the lumber
assortment from yellow birch or sugar maple stems by using a model that predicts the log
grading assortment from a standing tree quality (Fortin et al. 2009b). The predictions (i.e.,
log net volume) from the Fortin et al. (2009b) model could be integrated in our model that
uses log net volume as input. However, prior to such use, a model evaluation should be
performed on the final predictions resulting from both models, to assess potential issues
related to bias and error propagation.
Although the number and size of lumber pieces is mostly related to log dimensions, the final
product assortment is also modulated by complex trade-offs between optimizing for lumber
volume or lumber value (Auty et al. 2014). Thus, smaller pieces with better characteristics
(i.e., grades and colors) may be preferred to larger lumber pieces of lower quality, because
of their relatively higher market value. However, the processing cost of such smaller pieces
could also be higher. The sawing operator has to consider potential lumber grades, colors and
volumes throughout the sawing process in order to produce lumber with the overall highest
value. As a result, there could be a bias related to the sawmill operator. In our study, this bias
was minimized because the same skilled workers processed all conventional and bolt logs
from both study sites.
The use of the beta inflated distribution with abundance of zeros proved useful for predicting
lumber volume recovery. As it could be observed in figures 3.1 and 3.2, the assessment of
the dispersion parameter needs to be improved to better represent each lumber grade and
color category. We tested other distributions, where the values of the dependent variable were
87
not bound between 0 and 1, but these were associated with higher bias. Even with some
potential sources of bias and distribution problems, the predicted VRG and VRC per log were
close to the observed values. Therefore, we recommend using our models to obtain estimates
the volume recovery for a group or a population of logs. If they are used to generate
predictions for an individual log, the estimations could be inaccurate.
Conclusion
The objective of this study was to develop a set of models for predicting the lumber volume
recovery for grades and colors from external log characteristics in sugar maple and yellow
birch. No differences were found between these two species and they were considered
together in the assessment of the volume recovery related to lumber grades. The volume
recovery of the most valuable grades increased with log length and with the small-end
diameter of the log. In addition, the best lumber grades were found in the butt log. Log
dimensions were also positively related to the proportion of the most desired color
specifications, which did not contain red heartwood. Conversely, the red heartwood size was
related to the higher proportion of the regular (i.e., discolored) wood, that is less desirable
for both species, but also to a higher proportion of “Red Birch”, that generally has higher
value in yellow birch than the regular color. These variables were better predictors of volume
recovery than the specifically designed log grading rules. However, for a better accuracy,
they should be used to generate estimations of the volume recovery for a group of logs, rather
than at an individual level.
Acknowledgements
We are grateful to the Fonds de recherche du Québec – Nature et technologies (FRQNT) for
the financial support of this study. We wish to express our thanks to the staff from the
Ministère des Forêts, de la Faune et des Parcs du Québec (MFFP – Direction de la recherche
forestière), Station touristique de Duchesnay and Coopérative Forestière des Hautes-
Laurentides for providing and harvesting the sampling sites and to the staff of Centre de
recherche sur les matériaux renouvelables (CRMR) and FPInnovations for their assistance in
this project. The authors wish to acknowledge the valued collaboration of the staff from École
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de foresterie et de technologie du bois de Duchesnay for lumber processing and grading. We
are also grateful to Frauke Lenz, Élisabeth Dubé, Jean-Philippe Gagnon, Julie Barrette,
Emmanuel Duchateau and Normand Paradis for their assistance in the field work.
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Conclusion générale
Le succès d’un aménagement forestier étant lié de près à la qualité des arbres et des billes
produites (Erickson et al. 1992), il importe de favoriser la croissance des arbres sains et de
qualité, mais aussi de pouvoir évaluer cette qualité avant la récolte. L’objectif principal de
cette thèse était d’améliorer les prévisions d’approvisionnement des usines de transformation
de bois feuillu en reliant l’évaluation de la qualité des arbres sur pied à leur valeur monétaire
et au panier de produits transformés. L’érable à sucre et le bouleau jaune ont été choisis à
cause de leur abondance dans les forêts feuillues du Québec et leur importance commerciale.
En effet, les deux espèces sont principalement utilisées par l’industrie du sciage pour la
fabrication de divers produits dits « d’apparence », tels que les meubles et les parquets.
Le premier apport de cette thèse a permis de quantifier la proportion radiale de la coloration
de cœur des deux espèces dans 12 localisations couvrant l'ensemble de la zone tempérée du
sud du Québec. Un mesurage non destructif de la coloration de cœur en utilisant des carottes
de sondage a permis d’inventorier plusieurs arbres dans une vaste étendue, et ce, dans un
temps et aux coûts raisonnables. À notre connaissance, c’est la première étude scientifique
qui a mis en évidence le lien entre l’âge des arbres, leur vitesse de croissance et la proportion
de la zone colorée chez l’érable à sucre et le bouleau jaune. Des différences de la proportion
radiale de la coloration de cœur ont été observées entre les régions d’étude pour les deux
espèces et elles semblent être majoritairement attribuables à des facteurs liés au
développement des arbres. D’une part, nos résultats ont montré que l'âge cambial avait un
effet positif sur la proportion radiale de la coloration des deux espèces. La coloration de cœur
étant d’origine traumatique chez l’érable à sucre et le bouleau jaune, son développement et
sa propagation nécessitent des portes d’entrée dans l’arbre. L’effet d’âge observé serait ainsi
attribuable à une accumulation de blessures à travers le temps, principalement causées par la
mortalité des branches, et par une perte de vigueur de l’arbre (Giroud et al. 2008). Ces
résultats indiquent que l’occurrence de la coloration de cœur serait ultimement inévitable
chez les deux espèces. D’autre part, l’analyse de l’accroissement radial autour de la zone
colorée a révélé un effet positif de la superficie des anneaux de croissance à la limite de la
zone colorée et, dans le cas de l'érable à sucre, un effet négatif de la pente d’une régression
appliquée aux valeurs de superficie des anneaux couvrant une période de cinq ans de part et
90
d’autre de cette même limite. Conséquemment, pour un âge donné, une période de croissance
rapide suivie d’un ralentissement associé une récession de la cime favorisera le
développement d’une plus grande colonne de coloration. Au-delà des effets de l’âge et de
l’accroissement, une partie de la variabilité était aussi associée à la température minimale
annuelle d’une localisation dans le cas de l’érable à sucre. Cette variable climatique peut
favoriser l’apparition de gélivures et d’autres blessures dans l’arbre et semble liée de près à
la limite nordique de l’aire de distribution de l’érable à sucre. Par ailleurs, aucune autre
variable climatique n’a permis d’expliquer les variations régionales de la coloration de cœur,
et ce, même si un effet régional entre les sous-domaines bioclimatiques, caractérisés par
différents régimes de précipitations, a été observé pour l’érable à sucre.
Les résultats du deuxième chapitre ont permis de déterminer les principales variables qui
affectent la valeur monétaire de l’érable à sucre et du bouleau jaune sur pied. Un mesurage
détaillé de 64 érables à sucre et 32 bouleaux jaunes qui ont été dûment inspectés et classés,
avant d’être abattus, tronçonnés et transformés en planches, nous a permis d’établir que le
seuil maximal de valeur par mètre cube de bois rond pour l’érable à sucre et le bouleau jaune
se situait entre 40 et 45 cm de dhp. Ces résultats sont très proches de ceux du récent rapport
du Comité sur l'impact des modalités opérationnelles des traitements en forêt feuillue
(CIMOTFF) (Saucier et al. 2014), où il a été établi que pour les forêts du Québec, les
diamètres de maturité financière (i.e., diamètres au-delà duquel les arbres laissés sur pied
perdent de la valeur) pour la production de bois d’œuvre variaient de 46 à 50 cm pour l’érable
à sucre et le bouleau jaune. Dans notre étude, nous avons également observé une diminution
de la valeur par volume unitaire de bois rond avec une augmentation du diamètre des arbres
qui n’avaient aucun défaut apparent (ex. qualités A et B). Cela a permis de mettre en évidence
les limites des systèmes de classement de la qualité des arbres sur pied, qui ne sont pas en
mesure d’évaluer les défauts internes des arbres. Ils permettent aussi de questionner la
recommandation du CIMOTFF sur l’application d’un seuil de dhp au-delà duquel tous les
arbres devraient être récoltés. En effet, selon nos résultats, il serait pertinent d’ajouter un seuil
de dhp au-delà duquel un arbre devrait être laissé sur pied puisque sa qualité interne est
susceptible d’être faible, et ce, même s’il rencontre les critères externes l’associant aux
meilleures classes de qualité. Cette diminution de la valeur des tiges de bonne qualité a été
causée par une perte de volume liée à la carie. L’utilisation d’une sonde perceuse s’est avéré
91
un outil utile et complémentaire au classement visuel pour identifier les arbres cariés.
Toutefois, aucun lien n’a pu être établi entre le profil de la sonde perceuse et la présence de
coloration de cœur, qui diminue aussi la valeur des arbres, si cette coloration n’est pas
accompagnée de pourriture.
Les résultats du deuxième chapitre ont aussi mis en évidence le fait que parmi tous les types
de défauts qui doivent être pris en considération lors du marquage des arbres, les signes
visibles d’infection fongique et les fentes avaient la plus grande influence négative sur la
valeur des deux espèces. En n’utilisant que ces deux types de défaut dans nos systèmes
guidant la sélection des arbres, les critères de marquage des tiges peuvent être simplifiés, tout
en permettant d’assurer une évaluation de la qualité de l’arbre comparable aux systèmes plus
complexes. L’approche proposée est plus simple et moins coûteuse que celle des systèmes
complexes actuellement en place (p. ex., le système à quatre classes ABCD de Monger
(1991)). De plus, elle s’avère une solution de rechange aux approches dont l’efficacité n’a
pas été démontrée scientifiquement (p. ex., le système à deux classes O-P (MRNFQ 2006)).
Le troisième chapitre a mis en évidence le lien existant entre les caractéristiques des billes
destinées au sciage et les variables déterminantes qui font varier le rendement en produits
transformés. L’analyse des sciages a montré que la proportion des meilleurs grades augmente
avec la longueur et le diamètre des billes. De plus, le rendement en volume de sciages de
haute qualité était plus élevé dans le bas de l’arbre, parce que les grosses billes ont
généralement moins de défauts internes comme les nœuds. Chez l’érable à sucre, les
dimensions des billes de sciages étaient également positivement liées à un rendement plus
élevé en bois sans coloration, tandis que chez le bouleau jaune, elles étaient associées à une
plus forte proportion de la coloration de cœur. Dans tous les cas, les billes présentant une
grande zone colorée ont produit une forte proportion de bois « régulier » de valeur moindre.
Les modèles mis au point au troisième chapitre ont mieux prédit les rendements
volumétriques liés aux grades que les systèmes de classement de billes, ce qui indique qu’ils
pourraient remplacer les anciennes tables de rendement (Petro et Calvert 1976). D’autre part,
les modèles liés aux prévisions des rendements selon les couleurs des sciages constituent une
nouveauté permettant de mieux décrire le panier des produits transformés. Du point de vue
de la modélisation, le modèle de prévision du panier de produits de sciage pourrait être
92
intégré à un simulateur de croissance comme SaMARE (Fortin et al. 2009a). À partir des
prévisions du volume par catégorie de billes provenant des modèles de Fortin et al. (2009b),
il serait possible de prédire le rendement en grades et en couleurs des planches. Par contre,
avant une telle application, il faudra évaluer et minimiser les biais tout en analysant la
propagation des erreurs d’un modèle à l’autre.
En reprenant les principaux résultats de ce projet de recherche, l’étude de sciages nous a
montré que la valeur au m³ de bois rond des arbres sur pied diminuait après un certain seuil,
alors que la qualité moyenne des planches avait tendance à être plus élevée dans les grosses
billes. Ces résultats peuvent paraitre contradictoires au premier abord. En effet, le fait que les
grosses billes soient généralement de plus grande valeur suggère qu’il faudrait tendre vers
une sylviculture axée sur la production de gros arbres. Techniquement, cela pourrait être vrai
tant et aussi longtemps que ces gros arbres produisent des billes de sciage de qualité. Par
contre, la valeur au m³ de bois rond des arbres sur pied décroit après un certain seuil, puisque
ces arbres produisent moins de billes qui ont les caractéristiques nécessaires au sciage. Cela
met en évidence l’importance de voir la section transversale d’une bille, qui peut ou non être
rejetée du sciage, contrairement aux arbres sur pied pour lesquels les systèmes de classement
de la qualité ne sont pas en mesure d’évaluer les défauts internes. Il n’est pas simple de
déterminer le moment idéal pour couper un arbre en maximisant le volume et la qualité du
sciage, et donc sa valeur. Comme nous l’avons décrit précédemment, l’utilisation des seuils
diamétraux peut être une solution. De plus, l’âge de l’arbre devrait aussi idéalement être
considéré dans l’établissement des seuils, puisque à croissance égale, un arbre plus vieux
devrait avoir plus de défauts internes qu’un arbre plus jeune, entre autres à cause d’une plus
grande zone colorée. Toutefois, en pratique, l’âge des arbres n’est pas une variable connue
des sylviculteurs œuvrant dans les forêts feuillues de structure typiquement inéquienne. La
vaste gamme d’âge obtenue parmi les échantillons du premier article de cette thèse démontre
bien qu’il serait difficile d’estimer cette variable de manière juste.
Pour minimiser le développement de la coloration de cœur des arbres sur pied, tout en
maximisant la valeur des sciages, il est préférable d’avoir une croissance radiale lente en bas
âge, puis plus rapide par la suite. Ainsi, nous proposons de faire croitre les arbres sous forte
compétition lorsqu’ils sont jeunes afin de favoriser l’élagage naturel et limiter le nombre de
93
grosses branches. Par la suite, lorsque les arbres ont atteint une bonne hauteur de fût élagué,
un dégagement pourrait être fait pour augmenter la croissance radiale et ainsi favoriser la
production de billes de sciage (Baral et al. 2013). Les arbres ayant le meilleur potentiel pour
produire des sciages de qualité devraient être choisis comme des arbres d’avenir sur lesquels
appliquer ce scénario (Perkey and Wilkins 1993). En effet, un aménagement orienté vers la
production de petits arbres libres de croître, tout en maintenant une faible proportion de
grosses tiges résiduelles, peut être bénéfique pour la production de tiges destinées au sciage
(Buongiorno et al. 1993). D’autre part, les gros arbres ayant un faible accroissement ont une
probabilité de mortalité plus élevée (Woodall et al. 2005). Ainsi, l’aménagement des arbres
feuillus doit être orienté vers les individus qui ont un bon accroissement et qui possèdent un
potentiel d’amélioration du point de vue de qualité (Leak et al. 1987; Bastien and Wilhelm
2000). La très grande variabilité entre les âges des arbres échantillonnés au premier chapitre,
qui étaient pourtant de diamètres semblables et provenaient des mêmes stations, tend à
démontrer que l’environnement compétitif peut avoir un impact important sur la vitesse de
croissance radiale deux espèces.
Pour conclure, il a été démontré que la coupe de jardinage était très rarement appliquée selon
les règles de l’art, autant au Québec (Bédard and Brassard 2002) qu’au nord des États-Unis
(Pond et al. 2014). La volonté de restaurer le massif forestier, tout en assurant la rentabilité
des opérations forestières, s’est traduite par l’apparition de plusieurs traitements alternatifs
au jardinage ces dernières années (Saucier et al. 2014). Ces nouveaux traitements sylvicoles
et le retour vers un contexte plus favorable dans le secteur de la transformation du bois
(Fédération des producteurs forestiers du Québec 2015) font ressortir l’importance d’évaluer
avec justesse la qualité des arbres récoltés afin d’assurer un approvisionnement adéquat des
usines de transformation et des autres preneurs de bois feuillu. Les résultats de cette thèse
apportent plusieurs réponses face à cette problématique et peuvent avoir des retombées à
plusieurs niveaux. Tout d’abord, les modèles prévisionnels de la coloration de cœur et ceux
liés aux principaux défauts affectant la valeur des arbres sur pied peuvent servir d’outil au
sylviculteur lors de l’élaboration des prescriptions sylvicoles pour un peuplement. D’autre
part, l’identification visuelle des infections fongiques et des fentes en forêt peut être utilisée
pour améliorer les directives de martelage chez les feuillus. De plus, les modèles permettant
de prédire le rendement en grades ou en couleurs des sciages peuvent fournir aux producteurs
94
du bois une meilleure estimation du panier de produits, tout en offrant la possibilité d’être
intégrés dans les simulateurs de croissance. Finalement, dans cette étude, nous avons
uniquement considéré la valeur du bois découlant des produits transformés (sciages et pâte).
Afin de dresser un portrait économique et financier plus complet de la valeur des feuillus sur
pied, les recherches futures devraient, d’une part, inclure les coûts (p. ex., matière ligneuse,
transformation, etc.) et, d’autre part, considérer les autres utilisations possibles des bois
feuillus (p. ex., composés extractibles, granules, etc.), qui peuvent être complémentaires ou
non au sciage. De plus, les recherches futures pourraient porter sur les paniers de produits
alternatifs et de seconde transformation dans lesquelles certaines usines sont spécialisées,
plutôt que de se rattacher au bois de grade d’apparence, ce qui aurait l’avantage de se
rapprocher des marchés et d’une diversité de produits secondaires (p. ex., planchers,
ameublements, cabinets, etc).
95
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109
Annexe 1 : Données utilisées pour le chapitre 1
1A : Variables observées par site d’étude pour l’érable à sucre
ID Region name Stand
ID Latitude Longitude Elevation
Ecol.
type
Total stand
basal area
(m2/ha)
LT
Min
(°C)
MT
Mean
(°C)
Precip
(mm)
1 Témiscamingue 1 47°14'4" -78°47'47" 384 FE32 32.0 -43.8 2.1 1010.3
1 Témiscamingue 2 47°11'37" -79°8'30" 359 FE32 26.0 -41.8 2.6 973.4
2
Rapides-des-
Joachims 1 46°20'16" -77°44'39" 314 FE32 27.0 -37.7 3.6 946.4
2
Rapides-des-
Joachims 2 46°19'34" -77°41'20" 248 FE32 26.7 -36.8 4.1 925.8
3 Réservoir Cabonga 1 47°26'42" -77°2'22" 402 FE32 28.0 -45.1 1.4 961.5
3 Réservoir Cabonga 2 47°19'48" -76°56'20" 398 FE32 25.3 -44.5 1.6 965.3
4 Outaouais 1 46°30'40" -76°19'53" 411 FE32 26.0 -40.5 2.7 971.3
4 Outaouais 2 46°29'1" -76°18'54" 328 FE32 25.3 -39.8 3.1 967.5
5 Ste-Véronique 1 46°35'33" -74°58'38" 371 FE32 24.0 -40.0 3.1 1071.4
5 Ste-Véronique 2 46°33'45" -74°56'44" 347 FE32 31.3 -39.8 3.3 1069.2
6 Mauricie 1 46°51'43" -72°43'6" 319 FE32 29.0 -41.3 2.7 1103.4
6 Mauricie 2 46°48'17" -72°40'44" 276 FE32 27.2 -40.3 3.0 1118.1
7 Portneuf 1 47°8'30" -72°5'26" 416 FE32 30.0 -39.4 2.1 1247.0
7 Portneuf 2 47°3'59" -72°6'47" 376 FE32 28.0 -38.9 2.4 1256.8
8 Duchesnay 1 46°52'20" -71°40'20" 293 FE32 30.0 -36.5 3.1 1345.1
8 Duchesnay 2 46°55'22" -71°37'32" 225 FE32 21.0 -36.4 3.4 1349.0
9 Lac Mégantic 1 45°22'13" -70°56'55" 591 FE32 36.0 -33.4 3.6 1349.9
9 Lac Mégantic 2 45°26'23" -70°40'37" 544 FE32 38.0 -34.0 3.6 1170.9
10 Montmagny 1 46°51'39" -70°31'7" 367 FE32 19.3 -33.9 3.2 1208.4
10 Montmagny 2 46°50'55" -70°32'10" 361 FE32 29.0 -33.9 3.2 1210.5
11 Charlevoix 1 47°58'7" -69°57'10" 342 MS12 28.5 -34.6 2.0 1026.5
11 Charlevoix 2 47°57'16" -70°0'2" 296 FE32 28.0 -34.9 2.1 1010.1
12 Squatec 1 47°55'52" -68°30'39" 367 FE32 33.0 -36.0 2.2 1135.4
12 Squatec 2 47°54'39" -68°29'8" 408 FE32 23.0 -36.5 2.0 1142.2
110
1B : Variable observées par site d’étude pour le bouleau jaune
ID Region name Stand
ID Latitude Longitude Elevation
Ecol.
type
Total stand
basal area
(m2/ha)
LT
Min
(°C)
MT
Mean
(°C)
Precip
(mm)
1 Témiscamingue 1 47°15'16" -78°43'33" 364 FE32 27.3 -44.3 2.2 1007.0
1 Témiscamingue 2 47°13'18" -79°8'45" 327 MJ12 28.0 -41.8 2.7 955.1
2 Rapides-des-Joachims 1 46°19'34" -77°41'20" 248 FE32 26.7 -36.8 4.1 925.8
2 Rapides-des-Joachims 2 46°20'35" -77°43'6" 288 MJ12 29.0 -37.4 3.8 937.3
3 Réservoir Cabonga 1 47°26'42" -77°2'22" 402 FE32 28.0 -45.1 1.4 961.5
3 Réservoir Cabonga 2 47°19'48" -76°56'20" 398 FE32 25.3 -44.5 1.6 965.3
4 Outaouais 1 46°28'59" -76°18'45" 357 FE32 24.7 -40.0 3.0 968.3
4 Outaouais 2 46°29'59" -76°20'33" 352 FE32 28.0 -40.0 3.0 969.3
5 Ste-Véronique 1 46°36'39" -74°54'55" 344 MJ12 35.0 -40.0 3.3 1067.4
5 Ste-Véronique 2 46°33'45" -74°56'44" 347 FE32 31.3 -39.8 3.3 1069.2
6 Mauricie 1 46°49'16" -72°41'35" 343 FE32 20.0 -40.7 2.6 1116.7
6 Mauricie 2 46°48'17" -72°40'44" 276 FE32 27.2 -40.3 3.0 1118.1
7 Portneuf 1 47°11'43" -72°3'20" 493 MJ22 21.3 -40.3 1.6 1240.7
7 Portneuf 2 47°5'47" -72°6'27" 393 MJ12 29.0 -39.0 2.2 1260.7
8 Duchesnay 1 46°56'26" -71°44'9" 237 FE32 24.7 -36.0 3.4 1386.9
8 Duchesnay 2 46°55'22" -71°37'32" 225 FE32 23.0 -36.4 3.4 1349.0
9 Lac Mégantic 1 45°24'33" -70°40'13" 566 MJ12 27.0 -34.1 3.5 1181.6
9 Lac Mégantic 2 45°29'42" -71°9'39" 569 MJ12 24.0 -33.8 3.6 1424.1
10 Montmagny 1 46°51'36" -70°31'21" 362 MJ12 23.0 -33.9 3.2 1207.3
10 Montmagny 2 46°50'43" -70°31'34" 380 MJ12 25.0 -34.3 3.1 1216.1
11 Charlevoix 1 47°58'7" -69°57'10" 342 MS12 28.5 -34.6 2.0 1026.5
11 Charlevoix 2 47°57'16" -70°0'2" 296 FE32 28.0 -34.9 2.1 1010.1
12 Squatec 1 47°55'51" -68°30'40" 370 FE32 30.7 -36.1 2.2 1136.8
12 Squatec 2 47°55'28" -68°30'40" 413 FE32 32.0 -36.5 2.0 1149.7
111
1C : Variables dendrométriques pour l’érable à sucre
ID Region name Stand
ID N
Mean tree
DBH ± SD
(cm)
Mean tree
height ± SD
(m)
Mean tree
age ± SD
(years)
Mean
discoloration age
± SD (years)
Mean radius proportion
of discoloration ± SD
(%)
Mean basal area
proportion of
discoloration ± SD (%)
1 Témiscamingue 1 8 29.1 ± 3.1 20.1 ± 1.2 119 ± 19 65.5 ± 16.9 52.5 ± 11.8 28.7 ± 11.2
1 Témiscamingue 2 8 27.9 ± 3.0 19.7 ± 1.0 101 ± 24 54.6 ± 16.9 57.0 ± 6.9 32.9 ± 8.0
2 Rapides-des-Joachims 1 8 27.2 ± 2.9 20.7 ± 2.6 82 ± 7 37.6 ± 3.7 38.3 ± 6.1 15.0 ± 5.0
2 Rapides-des-Joachims 2 8 28.5 ± 3.1 21.8 ± 2.6 91 ± 27 42.5 ± 18.1 35.8 ± 7.7 13.3 ± 5.7
3 Réservoir Cabonga 1 8 30.0 ± 3.3 20.3 ± 1.7 114 ± 23 54.9 ± 13.8 41.9 ± 7.0 17.9 ± 5.3
3 Réservoir Cabonga 2 8 28.1 ± 3.1 19.1 ± 0.9 99 ± 25 49.6 ± 18.3 41.7 ± 12.4 18.8 ± 10.3
4 Outaouais 1 8 28.3 ± 2.8 22.2 ± 1.5 130 ± 9 77.9 ± 10.9 44.3 ± 6.9 20.1 ± 5.8
4 Outaouais 2 8 28.5 ± 3.4 20.8 ± 1.1 98 ± 22 50.8 ± 18.2 43.6 ± 9.7 19.8 ± 8.6
5 Ste-Véronique 1 8 27.5 ± 2.9 22.3 ± 1.5 108 ± 25 53.4 ± 23.7 40.5 ± 12.0 17.6 ± 9.9
5 Ste-Véronique 2 8 27.2 ± 2.8 19.4 ± 1.8 74 ± 10 31.9 ± 5.8 40.0 ± 10.6 17.0 ± 8.5
6 Mauricie 1 8 29.7 ± 2.8 22.6 ± 1.6 112 ± 23 51.8 ± 21.9 42.3 ± 8.1 18.4 ± 6.6
6 Mauricie 2 8 28.4 ± 3.0 19.2 ± 1.7 94 ± 8 41.6 ± 7.4 35.1 ± 12.4 13.7 ± 9.5
7 Portneuf 1 8 26.6 ± 2.2 20.2 ± 1.9 75 ± 15 33.6 ± 13.7 48.5 ± 9.2 24.2 ± 8.7
7 Portneuf 2 8 27.6 ± 2.4 20.1 ± 1.9 83 ± 12 38.5 ± 13.5 44.1 ± 10.4 20.4 ± 8.6
8 Duchesnay 1 8 28.8 ± 3.1 19.1 ± 1.0 94 ± 8 33.8 ± 7.3 42.7 ± 11.2 19.3 ± 9.7
8 Duchesnay 2 8 28.1 ± 2.4 22.8 ± 1.5 93 ± 23 44.1 ± 13.4 39.4 ± 9.0 16.2 ± 7.7
9 Lac Mégantic 1 8 30.8 ± 2.0 21.5 ± 1.9 78 ± 11 19.1 ± 9.7 21.6 ± 7.2 5.1 ± 3.1
9 Lac Mégantic 2 8 26.8 ± 2.0 22.7 ± 2.0 77 ± 5 28.8 ± 10.2 26.2 ± 14.0 8.6 ± 7.1
10 Montmagny 1 8 27.4 ± 3.0 21.4 ± 0.8 92 ± 17 28.4 ± 18.1 22.1 ± 16.6 7.3 ± 7.0
10 Montmagny 2 8 29.1 ± 2.8 21.1 ± 1.6 68 ± 9 19.0 ± 5.1 28.2 ± 12.2 9.2 ± 8.3
11 Charlevoix 1 8 28.9 ± 3.3 17.2 ± 1.5 94 ± 13 30.5 ± 7.4 24.5 ± 8.8 6.7 ± 4.8
11 Charlevoix 2 8 29.0 ± 2.9 17.3 ± 1.4 100 ± 28 33.4 ± 26.4 25.3 ± 18.8 9.5 ± 10.5
12 Squatec 1 8 27.8 ± 2.8 23.2 ± 1.2 82 ± 8 26.3 ± 15.2 23.3 ± 18.1 8.3 ± 9.7
12 Squatec 2 8 27.8 ± 2.1 20.5 ± 2.2 80 ± 9 21.5 ± 11.9 15.5 ± 11.0 3.5 ± 4.0
112
1D : Variables dendrométriques pour le bouleau jaune
ID Region name Site N
Mean tree
DBH ± SD
(cm)
Mean tree
height ± SD
(m)
Mean tree age
± SD (years)
Mean
discoloration age
± SD (years)
Mean radius
proportion of
discoloration ± SD
(%)
Mean basal area
proportion of
discoloration ± SD (%)
1 Témiscamingue 1 8 28.0 ± 2.9 19.3 ± 2.5 93 ± 8 41.3 ± 15.3 39.9 ± 19.2 19.1 ± 18.8
1 Témiscamingue 2 8 28.5 ± 2.1 18.7 ± 1.7 88 ± 16 33.8 ± 10.4 38.2 ± 7.4 15.0 ± 5.8
2 Rapides-des-Joachims 1 8 28.5 ± 1.9 21.4 ± 1.5 81 ± 27 36.5 ± 18.9 37.5 ± 10.0 15.0 ± 6.4
2 Rapides-des-Joachims 2 8 27.0 ± 2.1 19.6 ± 1.8 118 ± 18 55.4 ± 12.5 45.8 ± 10.6 22.0 ± 9.8
3 Réservoir Cabonga 1 8 28.6 ± 3.0 19.8 ± 2.0 105 ± 25 49.9 ± 14.7 43.0 ± 11.3 19.6 ± 9.0
3 Réservoir Cabonga 2 8 29.3 ± 3.6 19.4 ± 1.8 90 ± 13 42.3 ± 11.6 41.4 ± 11.2 18.3 ± 9.3
4 Outaouais 1 8 27.1 ± 3.0 19.7 ± 1.9 80 ± 19 30.9 ± 12.5 30.4 ± 12.5 10.6 ± 7.0
4 Outaouais 2 8 27.3 ± 2.7 19.8 ± 2.0 87 ± 27 39.5 ± 18.1 34.2 ± 12.2 13.0 ± 8.2
5 Ste-Véronique 1 8 27.9 ± 3.3 21.2 ± 1.9 98 ± 5 37.1 ± 8.8 49.2 ± 6.1 24.5 ± 5.9
5 Ste-Véronique 2 8 28.8 ± 3.0 21.4 ± 1.6 87 ± 7 29.0 ± 6.8 42.0 ± 9.0 18.3 ± 7.5
6 Mauricie 1 8 28.1 ± 3.4 19.3 ± 1.3 73 ± 33 31.0 ± 25.7 25.6 ± 15.3 8.6 ± 9.2
6 Mauricie 2 8 28.5 ± 2.5 20.5 ± 1.7 86 ± 12 41.1 ± 14.1 37.2 ± 12.9 15.3 ± 11.8
7 Portneuf 1 8 28.8 ± 3.0 16.2 ± 1.4 57 ± 23 13.4 ± 19.1 14.3 ± 13.9 3.7 ± 4.1
7 Portneuf 2 8 28.7 ± 3.5 19.4 ± 2.1 66 ± 18 26.6 ± 16.4 30.0 ± 13.5 10.6 ± 7.7
8 Duchesnay 1 8 28.1 ± 2.9 19.7 ± 1.3 68 ± 13 28.3 ± 10.1 39.5 ± 14.6 17.5 ± 10.6
8 Duchesnay 2 8 27.4 ± 2.6 23.5 ± 1.5 87 ± 12 44.3 ± 11.1 51.0 ± 11.5 27.2 ± 11.3
9 Lac Mégantic 1 8 27.7 ± 2.2 19.6 ± 1.2 74 ± 17 27.9 ± 7.9 29.5 ± 6.0 9.0 ± 3.3
9 Lac Mégantic 2 8 28.4 ± 2.4 19.0 ± 1.2 97 ± 9 44.6 ± 20.8 48.9 ± 14.4 25.7 ± 15.6
10 Montmagny 1 8 27.2 ± 3.5 19.9 ± 1.3 92 ± 9 44.0 ± 14.1 43.0 ± 11.4 19.6 ± 9.7
10 Montmagny 2 8 27.7 ± 2.3 19.3 ± 1.8 51 ± 5 11.8 ± 5.8 20.4 ± 8.7 4.8 ± 3.6
11 Charlevoix 1 8 27.3 ± 2.8 17.6 ± 0.9 70 ± 21 25.6 ± 14.0 26.2 ± 11.0 7.9 ± 5.5
11 Charlevoix 2 8 27.8 ± 3.1 17.2 ± 1.3 76 ± 18 24.3 ± 12.5 24.7 ± 9.6 6.9 ± 4.4
12 Squatec 1 8 27.9 ± 2.3 20.3 ± 2.3 79 ± 27 40.4 ± 27.2 45.9 ± 23.6 25.9 ± 17.0
12 Squatec 2 8 27.4 ± 2.8 20.5 ± 1.1 82 ± 38 44.3 ± 29.8 45.0 ± 20.4 23.9 ± 17.4
113
Annexe 2 : Données utilisées pour les chapitres 2 et 3
ID Site ID
Species DBH (cm)
Height (m)
Quality (Monger
1991)
Harvest priority (Boulet 2007)
Main defect (Boulet 2007)
Sound wood depth
(cm) (Resisto-graph)
Mean acoustic velocity
(m/s) (IML Hammer)
VAL ($/m³)
1 DU Sugar maple 39.7 22.5 B M FE06A 18.3 656.7 96.6
2 DU Sugar maple 23.5 20.6 C S EN03X 10.8 1238.8 47.0
3 DU Yellow birch 33.4 18.4 B C FE02A 11.8 1149.0 103.8
4 DU Yellow birch 26.6 17.0 D C FE02A 12.4 957.0 37.2
5 DU Yellow birch 34.7 19.9 C C NC07X 12.3 971.8 51.0
6 DU Sugar maple 47.5 21.2 C C FE06X 10.9 424.0 39.0
7 DU Sugar maple 30.1 18.8 C C VP01X 13.0 1157.5 44.7
8 DU Sugar maple 44.3 21.7 D S NC01X 3.3 481.0 42.0
9 DU Sugar maple 49.3 21.5 D M SP14A 12.3 411.2 25.6
10 DU Yellow birch 40.9 20.8 B M PR03A 5.3 596.0 41.4
11 DU Sugar maple 30.8 21.6 C M SP14A 7.8 826.7 39.4
12 DU Sugar maple 29.3 23.3 D M FE06A 7.3 488.2 35.4
13 DU Sugar maple 28.7 20.0 C R DB05X 10.8 1225.8 53.2
14 DU Yellow birch 38.1 17.9 D M SP15X 3.9 257.0 36.7
15 DU Yellow birch 62.4 23.2 A M PR03A 14.2 430.0 62.8
16 DU Sugar maple 35.2 19.0 B M FE06A 10.5 373.7 82.5
17 DU Sugar maple 28.0 21.6 D S DB05A 11.7 1291.0 54.7
18 DU Yellow birch 29.9 21.2 C M HP04X 14.1 918.0 63.0
19 DU Sugar maple 36.4 19.9 C M HP04X 15.0 1064.0 50.7
20 DU Yellow birch 39.3 25.6 A S EN03X 18.3 1128.2 103.8
21 DU Sugar maple 33.9 20.2 B R FE02X 15.7 1340.5 125.4
22 DU Sugar maple 42.7 25.8 C R FE02X 19.0 1163.0 110.5
23 DU Sugar maple 42.4 26.0 B C FE08X 19.5 690.0 81.6
24 DU Yellow birch 39.4 24.5 B R FE16X 16.1 1014.7 108.5
25 DU Sugar maple 46.1 24.7 A R HP01X 15.5 982.3 124.5
26 DU Sugar maple 40.5 24.7 A C FE06X 15.8 883.7 96.8
27 DU Sugar maple 39.3 17.5 B S DB05A 19.3 1333.3 83.4
28 DU Yellow birch 47.5 25.9 A R PR01X 21.6 1063.5 124.6
29 DU Yellow birch 31.0 23.7 C R EN01X 14.5 1054.0 92.3
30 DU Sugar maple 38.3 22.7 C S DB20A 14.9 1135.3 62.4
31 DU Yellow birch 42.5 22.5 A C NC07X 19.8 1120.7 128.5
32 DU Sugar maple 31.5 18.8 D C VP01X 13.3 1275.3 37.7
33 DU Sugar maple 37.7 22.0 B C EN04X 14.5 1215.8 94.6
34 DU Sugar maple 33.2 20.5 B S FE04A 14.3 1150.5 83.4
35 DU Yellow birch 38.8 26.2 B S EN03X 18.2 1159.5 121.8
36 DU Yellow birch 37.5 21.0 D R FE02X 17.6 1007.7 56.7
37 DU Sugar maple 24.6 22.9 D R FE02X 9.9 1207.0 46.2
38 DU Yellow birch 28.6 23.0 D S SP10X 4.3 477.8 35.1
39 DU Sugar maple 42.3 19.9 D C PR07X 12.0 753.0 46.2
40 DU Yellow birch 46.9 23.9 C S EN03X 18.2 823.8 64.2
41 DU Sugar maple 42.2 27.2 B R PR01X 16.4 1124.3 118.1
42 DU Sugar maple 37.2 22.0 B M SP14A 16.0 1269.7 113.7
43 DU Sugar maple 39.4 25.8 A R FE15X 18.7 1290.3 110.8
44 DU Sugar maple 46.7 25.0 B M PR03A 17.6 1024.8 81.5
45 DU Sugar maple 38.7 21.6 B S EN03X 17.8 1399.2 151.4
46 DU Sugar maple 58.5 26.4 B S EN03X 20.9 754.2 100.6
47 DU Sugar maple 40.7 20.0 A C EN04X 18.6 1304.0 137.2
48 DU Sugar maple 35.8 21.5 D R FE15X 14.5 1298.8 82.0
114
49 ML Yellow birch 46.9 23.5 B C FE06X 20.0 1089.8 62.7
50 ML Yellow birch 45.1 21.0 A R AR01X 20.8 998.3 99.9
51 ML Yellow birch 48.3 23.3 C S SP10X 16.6 1023.5 23.7
52 ML Yellow birch 48.8 20.8 B M FE06A 8.6 399.8 12.8
53 ML Yellow birch 42.4 21.8 A C FE06X 13.3 716.5 110.8
54 ML Yellow birch 28.1 20.7 C C DB10X 13.6 813.5 34.0
55 ML Yellow birch 31.4 22.9 C R DB05X 15.1 913.0 80.4
56 ML Yellow birch 31.9 24.1 D C DB10X 13.4 586.3 19.6
57 ML Yellow birch 49.5 23.2 A M HP07X 15.3 955.8 68.0
58 ML Yellow birch 38.2 25.7 B R PR01X 18.1 1008.8 66.9
59 ML Yellow birch 32.6 22.2 C M NC02X 9.3 705.5 51.1
60 ML Yellow birch 44.7 22.7 D M NC07A 15.1 934.2 17.4
61 ML Yellow birch 40.7 22.0 A S SP10X 18.4 1047.0 60.2
62 ML Yellow birch 38.9 24.6 B S EN03X 15.5 852.3 38.6
63 ML Yellow birch 32.9 21.1 D S EN03X 15.1 815.0 35.5
64 ML Yellow birch 34.2 21.3 D R FE02X 15.7 1031.5 50.1
65 ML Sugar maple 43.0 21.7 A S EN03X 19.5 1191.3 65.7
66 ML Sugar maple 37.3 18.6 C R DB05X 15.4 629.0 64.1
67 ML Sugar maple 37.1 20.0 D R FE01X 16.3 854.8 40.7
68 ML Sugar maple 37.2 22.2 C M SP14A 13.5 1111.5 55.3
69 ML Sugar maple 25.4 18.8 D R DB05X 7.7 806.3 14.2
70 ML Sugar maple 44.1 20.4 A R AR01X 20.5 1194.7 88.1
71 ML Sugar maple 36.5 25.0 C S SP09X 13.3 1096.8 45.4
72 ML Sugar maple 37.5 22.2 C C FE08X 13.0 895.5 37.1
73 ML Sugar maple 46.8 22.3 A M VP02X 19.1 1029.5 31.8
74 ML Sugar maple 30.0 18.9 C M SP14A 6.1 655.2 19.4
75 ML Sugar maple 27.2 18.8 C S VP01A 12.3 806.8 59.5
76 ML Sugar maple 29.7 20.9 C C VP01X 13.3 1204.8 57.3
77 ML Sugar maple 44.7 25.1 A M FE06A 16.2 895.8 74.6
78 ML Sugar maple 39.7 22.5 B C FE06X 11.6 947.5 58.1
79 ML Sugar maple 44.0 20.1 B S HP11A 17.8 1007.0 49.2
80 ML Sugar maple 32.1 21.8 D M NC07A 10.1 664.7 24.3
81 ML Sugar maple 32.9 18.6 D S EN03X 14.6 1193.0 61.0
82 ML Sugar maple 36.9 19.4 B S VP01A 13.7 1164.7 64.6
83 ML Sugar maple 50.5 21.0 A R FE02X 13.1 426.3 33.1
84 ML Sugar maple 38.8 21.0 D M SP08X 5.1 627.8 30.3
85 ML Sugar maple 36.4 19.0 B R DB14X 15.4 564.3 55.9
86 ML Sugar maple 55.0 26.2 A C VP01X 11.5 480.8 31.4
87 ML Sugar maple 36.2 22.8 B C DB20X 16.7 1342.2 80.2
88 ML Sugar maple 32.5 22.6 C R AR01X 14.8 1284.5 53.2
89 ML Sugar maple 26.2 17.2 D C DB10X 7.5 566.0 32.5
90 ML Sugar maple 48.7 21.3 B R DB05X 19.6 728.3 79.7
91 ML Sugar maple 35.1 17.6 B M SP16X 7.6 980.0 26.8
92 ML Sugar maple 41.1 24.1 A C FE06X 17.9 748.7 63.4
93 ML Sugar maple 50.1 18.2 B M SP12X 11.1 956.8 13.2
94 ML Sugar maple 40.2 24.8 D S SP09X 10.8 1071.5 51.1
95 ML Sugar maple 34.8 21.9 D C FE06X 12.6 652.8 16.6
96 ML Sugar maple 53.3 25.5 A S NC01X 20.8 944.3 54.1