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Yield tables are used to identify trends in growing space efficiency (GSE) and to relate GSE to self-tolerance and intraspecific competition. The method is useful when data specifically collected for this purpose are not available. Plonski's normal yield tables for jack pine (Pinus banksiana Lamb.), paper birch (Betula papyrifera Marshall), trembling aspen (Populus tremuloides Michx.), and black spruce (Picea mariana (Mill.) B.S.P.) are used. An exponential volume-age function was partitioned into volume-area and area-age functions. The exponents of these two components form the B/D ratio, which is used to determine the mode of the stand at a given time, e.g., if B/D is <3/2, then the stand is in area occupation mode, and if B/D is >3/2, then the stand is in area exploitation mode. The dominant mode is the one most responsive to availability of growth resources, showing greater acceleration when resources are plentiful and more rapid deceleration when resources are scarce. Jack pine and paper birch are identified as area occupiers, whereas trembling aspen and black spruce are area exploiters and are therfore self-tolerant. Asymmetric competition was deemed to be present for paper birch throughout the life of the stand on site class I and for trembling aspen on all sites prior to senescence. Les tables de production sont utilisées pour identifier les tendances de l'efficacité à utiliser l'espace de croissance (EEC) et pour relier l'EEC à l'auto-tolérance et à la compétition intraspécifique. La méthode est utile lorsque des données spécifiquement récoltées à cette fin ne sont pas disponibles. Les tables normales de production de Plonski pour le pin gris (Pinus banksiana Lamb.), le bouleau à papier (Betula papyrifera Marshall), le peuplier faux-tremble (Populus tremuloides Michx.) et l'épinette noire (Picea mariana (Mill.) B.S.P.) ont été utilisées. Une fonction exponentielle reliant le volume à l'âge a été séparée en fonctions reliant le volume à la surface et la surface à l'âge. Les exposants de ces deux composantes forment le rapport entre B et D qui est utilisé pour déterminer le mode du peuplement à un temps donné; p. ex. si B/D est plus petit que 3/2, le peuplement est dans un mode d'occupation de la surface et, si B/D est plus grand que 3/2, le peuplement est dans un mode d'exploitation de la surface. Le mode dominant est celui qui réagit le plus à la disponibilité des ressources qui supportent la croissance; il est associé à une plus forte accélération quand les ressources sont abondantes et à une plus forte décélération lorsque les ressources sont rares. Le pin gris et le bouleau à papier sont identifiés comme des occupants de la surface alors que le peuplier faux-tremble et l'épinette noire sont des exploitants et sont, par conséquent, auto-tolérants. Nous avons jugé qu'une compétition asymétrique était présente dans le cas du bouleau à papier tout au long de la vie d'un peuplement établi sur une station de qualité I et, dans le cas du peuplier, sur toutes les stations avant la période de sénescence. [ABSTRACT FROM AUTHOR]

Variation in canopy composition can influence ecosystem processes, such as nutrient cycling and light transmittance, even when environmental soil conditions are similar. To determine whether forest cover type influences species composition of the understory vegetation (herbs and shrubs), the composition of this layer was studied on two different surface deposits, clay and till, and under four different forest cover types dominated, respectively, by Populus tremuloïdes Michx. (aspen), Betula papyrifera Marsh. (white birch), Pinus banksiana Lamb. (jack pine), and Picea glauca (Moench) Voss – Abies balsamea (L.) Mill. (spruce–fir) over similar environmental conditions. Detrended correspondence analysis and analysis of variance performed on the ordination scores revealed that understory plant composition was highly affected by surface deposit and forest cover. The gradient observed in the correspondence analysis proceeds from aspen, white birch, spruce–fir, to jack pine. Indicator species were identified for each surface deposit and cover type, and most of them were associated with either jack pine or aspen. The richness, evenness, and diversity of the understory vegetation did not vary between cover types, but were affected by surface deposit. By controlling ecosystem processes such as light transmittance and nutrient cycling, forest cover influences understory composition.Key words: cover, understory, composition, boreal forest, environmental condition.La composition du peuplement peut affecter les processus écosystémiques, tels que le cycle des éléments nutritifs et la transmission lumineuse, malgré la présence de conditions environnementales similaires. Afin de vérifier si le couvert arborescent influence la composition de la strate de sous-bois, des relevés de la végétation herbacée et arbustive ont été effectués dans des conditions environnementales détendancées similaires, incluant deux dépôts de surface différents, till et argile, et quatre couverts forestiers dominés respectivement par les Populus tremuloïdes Michx. (peuplier faux-tremble), Betula papyrifera Marsh. (bouleau blanc), Pinus banksiana Lamb. (pin gris) et Picea glauca (Moench) Voss et Abies balsamea (L.) Mill. (épinette–sapin). L'analyse des correspondances détendancées et l'analyse de variance effectuées sur les coordonnées des axes de l'ordination révèlent un effet du dépôt de surface et du couvert arborescent. Le gradient observé en analyse des correspondances va du peuplier faux-tremble, bouleau blanc, mélange de conifères, au pin gris. Des espèces indicatrices ont été identifiées pour chacun des dépôts de surface et couverts forestiers, et la majorité d'entre-elles étaient associées soit au pin gris soit au peuplier faux-tremble. La richesse, l'équitabilité et la diversité de la strate de sous-bois ne varient pas en fonction du couvert forestier, mais sont significativement affectées par le dépôt de surface. Les différents processus écosystémiques, tels que la transmission de la lumière et le cycle des éléments nutritifs, semblent expliquer l'influence du couvert forestier sur la composition de la strate de sous-bois.Mots clés : couvert, sous-bois, composition, forêt boréale, condition environnementale. [ABSTRACT FROM AUTHOR]

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Copyright of Canadian Journal of Forest Research is the property of Canadian Science Publishing and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Forest plantations play an increasingly important role in meeting global demand for wood. They usually have higher yield than naturally regenerated forests. Thus, plantations can support economically viable wood production, enable forest conservation elsewere, help mitigate climate change by contributing to carbon sequestration and increase forest resilience and resistance to biotic and abiotic stressors. If yield of plantations is not as high as anticipated, then their use could generate important sustainability issues. There are still major gaps in our understanding of the factors that influence yield, even with respect to black spruce, white spruce, and jack pine, three of the most commonly planted tree species in northeastern North America. Our objective was to evaluate the yield of forest plantations of these species over a 416 000 km2 region that was representative of northeastern North American forests. Contrary to our prediction, realized yield of operational plantations was consistently lower than anticipated. Site index and competition both played a significant role in determining the yield of plantations. In the context of uncertain realized yield of operational plantations, we emphasize the necessity of relying on adaptive management to determine harvest levels that are compatible with sustainable management objectives. [ABSTRACT FROM AUTHOR]

Individual tree diameter at breast height (DBH) distribution is an important information for forest management planning. Forest managers obtain the DBH data either by field measurements or estimations using predictive models. However, probability distribution models are still lacking or need improvement. Therefore, we aimed to construct and fit diameter distribution models that reflect forest structure and composition change. We evaluated gamma, log-normal, and Weibull probability distribution functions (PDFs) for two commercially important tree species, black spruce (Picea mariana (Mill) B.S.P.) and jack pine (Pinus banksiana Lamb), grown in natural stands across Ontario, Canada. We modelled the parameters of the distributions as a function of stand-level variables for these species. We used DBH data from 735 permanent sample plots. Our results showed that all three evaluated PDFs reflected observed DBH distribution. We demonstrated that the moment-based recovered parameters could represent the maximum likelihood-estimated parameters precisely, and parameters of the PDFs can be modelled as a function of stand-level dynamic covariates. The models unbiasedly predicted the PDF parameters DBH means and DBH classes. The R2 of the model fit ranged between 0.35 and 0.98 for the predicted parameters and 0.90 and 0.97 for the predicted DBH. [ABSTRACT FROM AUTHOR]

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Fungi are primary agents of coarse woody debris (CWD) decay in boreal forests, playing an essential role in nutrient cycling and carbon storage. We compared fungal community assemblages using alpha and beta diversity metrics, and physical and chemical properties of CWD across three tree species (trembling aspen [Populus tremuloides], black spruce [Picea mariana], and jack pine [Pinus banksiana]), five decay classes, and two stand development stages, differing in time since stand replacing disturbance in Ontario's boreal forest region. We sampled 180 individual CWD logs from 6 independent stands, with 3 replicates per each species × decay class combination at each site. Using high-throughput sequencing of marker DNA, we found that fungal community structure significantly differed across tree species, decay stage, and stand age. Fungal diversity was highest in decay class 4 CWD. We found that Mn and K concentrations, total carbon, C/N ratio, N/P ratio, and moisture content were important predictors of fungal composition across CWD species and/or decay stage. This study suggests that forest management guidelines that consider both deadwood quantity and quality will support a broader range of fungal species and communities through post-disturbance stand development. [ABSTRACT FROM AUTHOR]

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This paper examined the impact of commercial thinning on selected wood properties of jack pine (Pinus banksiana Lamb.). Wood properties evaluated include wood density (ring density, earlywood ring density, and latewood ring density), percentage of latewood in the ring, and wood bending properties. Nonlinear, mixed-effect models have been developed using data from three commercially thinned sites in eastern Canada. Ring density followed the same pattern as percentage of latewood, in which cambial age, relative height, and ring width were found to have important effects. Earlywood and latewood ring densities changed within the juvenile wood zone until a plateau was reached. Ring width affected earlywood and latewood ring densities mainly in narrow rings. Wood bending stiffness (measured by modulus of elasticity) and strength (measured by modulus of rupture) increased with cambial age and wood density; whereas, wood strength was also affected by ring width. Commercial thinning did not influence the developed models, but it had an indirect effect through increased ring width. Cette étude a examiné l’impact de l’éclaircie commerciale sur certaines propriétés du bois de pin gris (Pinus banksiana Lamb.). Ces propriétés incluaient la densité du bois (densité des cernes, densité du bois initial et densité du bois final), la proportion de bois final dans chaque cerne et les propriétés mécaniques en flexion. Des modèles non linéaires mixtes ont été développés à partir de données provenant de trois stations qui avaient subi une éclaircie commerciale dans l’est du Canada. La densité des cernes s’est révélée être fortement influencée par l’âge cambial, la hauteur relative et la largeur des cernes, suivant ainsi un patron de variation similaire à celui de la proportion de bois final. La densité du bois initial et celle du bois final ont changé à l’intérieur de la zone de bois juvénile pour atteindre un plateau par la suite. La largeur des cernes a aussi affecté ces densités, en particulier dans le cas des cernes étroits. Les modules d’élasticité (MOE) et de rupture (MOR) en flexion ont augmenté avec l’âge cambial et la densité du bois. De plus, le module de rupture a été affecté par la largeur des cernes. L’éclaircie commerciale n’a pas changé les paramètres des modèles, mais elle a eu une influence indirecte à cause de son effet sur la largeur des cernes. [ABSTRACT FROM AUTHOR]

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Copyright of Canadian Journal of Plant Science is the property of Canadian Science Publishing and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Purpling of the needles of jack pine seedlings in forest tree nurseries in the autumn is a result of the production of at least five anthocyanin pigments: cyanidin 3-O-glucoside (~80%), delphinidin 3-O-glucoside (~8%), peonidin 3-O-glucoside (~8%), petunidin 3-O-glucoside (~3%) and malvidin 3-O-glucoside (trace). The twigs subtending the needles also produce a similar range of pigments. The entire spectrum of pigments is produced from the time of the first exposure to freezing temperatures. Proanthocyanidins are a prominent feature of the needle phenolics and the question of their possible involvement in the purpling phenomenon following exposure to sub-zero temperatures is raised. The red colour of the hypocotyl of the newly germinated seedling is also a result of a similar mixture of pigments.Key words: Pinus banksiana, Pinaceae, jack pine seedlings, anthocyanin pigmentation, hypocotyl, proanthocyanidins.La couleur pourpre que prennent les aiguilles des plants de pin gris des pépinières forestières, à l'automne, est occasionnée par la production d'au moins cinq pigments anthocyaniques : cyanidine 3-O-glucoside (~80 %), delphidine 3-O-glucoside (~8 %), péonidine 3-O-glucoside (~8 %), pétunidine 3-O-glucoside (~3 %), et malvidine 3-O-glucoside (trace). Les ramilles supportant les aiguilles produisent également un tel ensemble de pigments. La totalité du spectre des pigments est produite dès la première exposition au gel. Les proanthocyanidines constituent une caractéristique des phénols aciculaires et les auteurs soulèvent la possibilité de leur implication dans le phénomène de la coloration pourpre suite au gel. La couleur rouge de l'hypocotyle des graines récemment germées résulte d'un mélange des mêmes pigments. Mots clés : Pinus banksiana, Pinaceae, plantules de pin gris, pigmentation anthocyanique, hypocotyle, proanthocyanidines. [Traduit par la Rédaction] [ABSTRACT FROM AUTHOR]

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Copyright of Botany is the property of Canadian Science Publishing and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Canadian Journal of Forest Research is the property of Canadian Science Publishing and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Canadian Journal of Forest Research is the property of Canadian Science Publishing and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Canadian Journal of Forest Research is the property of Canadian Science Publishing and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Canadian Journal of Forest Research is the property of Canadian Science Publishing and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Canadian Journal of Forest Research is the property of Canadian Science Publishing and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Canadian Journal of Forest Research is the property of Canadian Science Publishing and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Botany is the property of Canadian Science Publishing and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Canadian Journal of Forest Research is the property of Canadian Science Publishing and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Dominant tree species and anthropogenic disturbances influence understory taxonomic diversity (TD) and species traits (functional diversity, FD) in managed forests. We compared understory TD and FD in managed jack pine (Pinus banksiana Lamb.) stands and red pine (Pinus resinosa Ait.) plantations. Understory herbs, grasses, shrubs, and nonvascular species were assessed in 1 m2 quadrats on two perpendicular line transects. Data were analyzed using generalised least squares regression, and multivariate fourth corner and RLQ analyses. Although there were few differences in understory species communities, red pine plantations appeared to impose weak environmental filters on TD in ways that were absent from the jack pine stands. Taxonomic diversity declined with age in red pine but not in jack pine, and may have been affected by the accumulation of litter cover in red pine stands. Although vegetation cover was lower in red pine than in jack pine, species richness on a percent cover basis was greater, and saturated at high cover levels in jack pine. Functional richness and evenness were unaffected by overstory species, but high litter cover favoured higher values of functional divergence. These results imply that there was a high level of functional redundancy among species for the suite of traits that we analyzed. [ABSTRACT FROM AUTHOR]

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Copyright of Canadian Journal of Forest Research is the property of Canadian Science Publishing and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Canadian Journal of Forest Research is the property of Canadian Science Publishing and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Canadian Journal of Forest Research is the property of Canadian Science Publishing and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Canadian Journal of Forest Research is the property of Canadian Science Publishing and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Canadian Journal of Forest Research is the property of Canadian Science Publishing and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Canadian Journal of Forest Research is the property of Canadian Science Publishing and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Canadian Journal of Forest Research is the property of Canadian Science Publishing and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Canadian Journal of Forest Research is the property of Canadian Science Publishing and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Canadian Journal of Forest Research is the property of Canadian Science Publishing and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Canadian Journal of Forest Research is the property of Canadian Science Publishing and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Canadian Journal of Forest Research is the property of Canadian Science Publishing and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Canadian Journal of Forest Research is the property of Canadian Science Publishing and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Canadian Journal of Forest Research is the property of Canadian Science Publishing and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

A correction to the article "Crown Fire Behaviour in a Northern Jack Pine--Black Spruce Forest" is presented.

We investigated the frequency of root grafting in naturally and artificially regenerated stands of jack pine (Pinus banksiana Lamb.) in the western boreal forest of Quebec, Canada. Twelve 30–60 m2 plots were hydraulically excavated to determine effects of site characteristics on frequency and timing of root grafting. Naturally regenerated stands had grafted tree percentages similar to artificially regenerated stands (21%–71% across plots) but greater numbers of root grafts per tree (naturally regenerated, 0.73 graft·tree–1; artificially regenerated, 0.52 graft·tree–1). Mean percentages of grafted trees, number of grafts per tree, and the speed of graft formation were greater in sandy soils (61%, 0.71 graft·tree–1 and 2.43 years, respectively) compared with clay soils (44%, 0.54 graft·tree–1 and 2.97 years, respectively). Proximity of trees was a better predictor of root grafting than stand density, despite many root grafts being found with distant trees (>2 m) in artificially regenerated stands. Our results suggested that root grafts form early in stand development. Even if trees are initially separate entities, this relatively high level of root grafting produces stands where trees are extensively interconnected. Nous avons étudié la fréquence des greffes racinaires dans des peuplements de pin gris (Pinus banksiana Lamb.) d’origines naturelle et artificielle dans la forêt boréale de l’ouest du Québec, au Canada. Douze parcelles de 30 à 60 m2 ont été excavées à l’aide d’un jet d’eau pour déterminer les effets des caractéristiques de la station sur la fréquence et la période de formation des greffes racinaires. Les peuplements régénérés naturellement avaient des pourcentages d’arbres greffés semblables à ceux des peuplements régénérés artificiellement (de 21 % à 71 % dans l’ensemble des placettes), mais avaient un plus grand nombre de greffes par arbre (régénérés naturellement : 0,73 greffe·arbre–1; régénérés artificiellement : 0,52 greffe·arbre–1). Le pourcentage moyen d’arbres greffés, le nombre de greffes par arbre et la vitesse de formation des greffes étaient plus élevés dans les sols sableux (respectivement 61 %, 0,71 greffe·arbre–1 et 2,43 années) que dans les sols argileux (respectivement 44 %, 0,54 greffe·arbre–1 et 2,97 années). La proximité des arbres était une meilleure variable prédictive des greffes racinaires que la densité des peuplements, même si plusieurs greffes racinaires ont été observées entre des arbres distants de plus de 2 m dans les peuplements régénérés artificiellement. Nos résultats indiquent que les greffes racinaires se forment tôt au cours du développement d’un peuplement. Même si les arbres sont des entités initialement séparées, le nombre relativement élevé de greffes racinaires produit des peuplements dans lesquels les arbres sont abondamment interconnectés. [ABSTRACT FROM AUTHOR]

Mineral soils exposed by fire are often covered by a layer of ash due to complete consumption of the forest floor (litter and duff). To assess the possible effects of ash on seed germination and viability of jack pine (Pinus banksiana Lamb.), black spruce (Picea mariana (Mill.) Britton, Sterns, Poggenb.), white spruce (Picea glauca (Moench) Voss), and balsam fir (Abies balsamea (L.) Mill.), a laboratory experiment was conducted using ash derived from three types of forest floor samples. The samples represented areas of high conifer concentration, high aspen concentration, and mixed aspen and conifer and were collected from five mature aspen (Populus tremuloides Michx.) – conifer mixedwood stands in southeastern Manitoba. Ash derived from each forest floor type neither prohibited nor delayed conifer germination, except that of balsam fir. Balsam fir had significantly less germination on ash derived from forest floor samples with high aspen concentration. When corrected for seed viability, balsam fir had significantly less germination on all three ash types compared with jack pine, black spruce, and white spruce. However, the impact of ash on balsam fir is unlikely to have meaningful ecological implications, as balsam fir is a climax species and will establish in undisturbed mature forests. Le sol minéral exposé par le feu est souvent recouvert d’une couche de cendre due à la combustion de la couverture morte (litière et humus). Les effets de la cendre sur la viabilité et la germination des graines de pin gris (Pinus banksiana Lamb.), d’épinette noire (Picea mariana (Mill.) Britton, Sterns, Poggenb.), d’épinette blanche (Picea glauca (Moench) Voss) et de sapin baumier (Abies balsamea (L.) Mill.) ont été évalués. Une expérience en laboratoire a été réalisée en utilisant de la cendre provenant de trois types d’échantillons de couverture morte, représentatifs de zones avec une concentration élevée de conifères (HC), de peupliers (LC) et d’un mélange de peupliers et de conifères (MC) prélevés dans cinq peuplements mixtes matures de peuplier faux-tremble (Populus tremuloides Michx.) dans le sud-est du Manitoba. La cendre provenant de chacun des types de couverture morte n’a ni inhibé ni retardé la germination des conifères à l’exception du sapin baumier. Les graines de sapin baumier germaient significativement moins bien sur la cendre provenant du type de couverture morte LC. Lorsqu’elle était corrigée pour la viabilité des graines, la germination du sapin baumier était significativement plus faible sur les trois types de cendre comparativement au pin gris, à l’épinette noire et à l’épinette blanche. L’impact de la cendre sur le sapin baumier a peu de chances d’avoir des implications écologiques significatives étant donné que le sapin baumier est une espèce climacique qui s’établira dans les forêts matures non perturbées. [ABSTRACT FROM AUTHOR]

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