Feeding Sites of Aphids of the Genus Cinara Curtis (Homoptera: Aphididae) in Northwestern Ontario

1959 ◽  
Vol 91 (10) ◽  
pp. 670-671 ◽  
Author(s):  
G. A. Bradley
Keyword(s):  
Black Spruce ◽  
Jack Pine ◽  
Red Pine ◽  
Balsam Fir ◽  
White Pine ◽  
White Cedar ◽  
Feeding Sites ◽  
Red Lake ◽  
Northwestern Ontario ◽  
Common Juniper

While working at Cedar Lake in Northwestern Ontario in the summers of 1957 and 1958 the author was able to observe the feeding sites of various species of Cinara. Most of the observations were made within an area of a few square miles on either side of Highway 105, between Red Lake Road and Ear Falls, Ontario. This area is fairly typical of the Laurentian Shield, with numerous lakes, rocky ridges, sandy patches, and small bogs. The principal coniferous trees in this locality are black spruce, jack pine, and balsam fir. White spruce, white cedar, white pine, red pine, and common juniper are also present.

Critical period of interspecific competition for four northern conifers: 10-year growth response and associated vegetation dynamics

2006 ◽  
Vol 36 (10) ◽  
pp. 2474-2485 ◽  
Author(s):  
Robert G Wagner ◽  
Andrew P Robinson
Keyword(s):  
Interspecific Competition ◽  
Critical Period ◽  
Black Spruce ◽  
Jack Pine ◽  
Red Pine ◽  
Growth Responses ◽  
White Pine ◽  
Conifer Species ◽  
Stand Volume ◽  
Vegetation Control

The influence of the timing and duration of interspecific competition on planted jack pine (Pinus banksiana Lamb.), red pine (Pinus resinosa Ait.), eastern white pine (Pinus strobus L.), and black spruce (Picea mariana (Mill.) BSP) was assessed using 10-year growth responses in a northern Ontario experiment. Stand volume was 117%, 208%, 224%, and 343% higher for jack pine, red pine, white pine, and black spruce, respectively, with 5 years of vegetation control than with no vegetation control. Stand volume increased linearly with number of years of vegetation control, and the slope of the relationship varied among conifer species. Change-point regression analysis was used to derive segmented weed-free and weed-infested curves, and to simultaneously estimate key critical-period parameters. Weed-free and weed-infested curves in the 10th year were similar to those derived in year 5, indicating that the patterns established during the first few years after planting were relatively robust for the first decade. The critical-period was 2 and 3 years after planting for jack pine and red pine, respectively, and occupied most of the 5-year period for white pine and black spruce. Principal components analysis of the vegetation community indicated that repeated herbicide applications caused differential shifts in the relative abundance of shrub, fern, and moss species through the 10th year. Species richness, however, was not substantially different between the untreated control and the most intensive treatments. Difference modeling was used to quantify how annual volume increment during the first decade varied with time, conifer species, cover of woody and herbaceous vegetation, and stage of development.

Critical period of interspecific competition for northern conifers associated with herbaceous vegetation

1999 ◽  
Vol 29 (7) ◽  
pp. 890-897 ◽  
Author(s):  
Robert G Wagner ◽  
Gina H Mohammed ◽  
Thomas L Noland
Keyword(s):  
Interspecific Competition ◽  
Critical Period ◽  
Black Spruce ◽  
Volume Growth ◽  
Jack Pine ◽  
Red Pine ◽  
Volume Index ◽  
Stem Volume ◽  
White Pine ◽  
Herbaceous Vegetation

Using critical-period analysis, we examined the temporal effects of interspecific competition from herbaceous vegetation on seedlings of jack pine (Pinus banksiana Lamb.), red pine (Pinus resinosa Ait.), eastern white pine (Pinus strobus L.), and black spruce (Picea mariana (Mill.) BSP) during the first 5 years after planting. The critical period is the time period during stand development when interspecific competition reduces tree growth. We found both similarities and differences in responses among tree species. Gains in stem volume index associated with increasing duration of vegetation control (expressed by weed-free curves) differed among species. In contrast, declines in stem volume index with increasing duration of competition after planting (expressed by weed-infested curves) were equal among species. Critical periods for stem volume index were shorter for shade-intolerant jack and red pine (1 and 2 years after planting) than for more shade-tolerant white pine and black spruce (1-3 years for spruce and 1-4 years for white pine). Intolerant species had greater absolute stem volume growth, but smaller relative declines from continuous association with herbaceous vegetation (85, 81, 78, and 67% for white pine, black spruce, red pine, and jack pine, respectively). Herbaceous vegetation did not affect survival and had a variable influence on height growth of all species.

An investigation of product form

1984 ◽  
Vol 14 (6) ◽  
pp. 768-774 ◽  
Author(s):  
P. Roebbelen ◽  
V. G. Smith
Keyword(s):  
Black Spruce ◽  
Jack Pine ◽  
Small Sample ◽  
Red Pine ◽  
Product Form ◽  
Regression Equations ◽  
White Pine ◽  
Total Height ◽  
Breast Height ◽  
Diameter Outside Bark

Product form (P) of a tree has been defined as the product of diameter-outside-bark at midheight above breast height (d) and total height (H) (P = d × H). It is used along with diameter breast height (D) in product form volume equations (VPF = f(P,D)) for estimating individual tree volumes. It is hypothesized that for each coniferous species, there exists some optimal height at which a diameter measurement can be taken and used in a product form term to estimate the inside-bark volume with minimum error. Regression equations and simpler expressions of the form V = D2 × H × F were developed for red pine (Pinusresinosa Ait.), white pine (Pinusstrobus L.), jack pine (Pinusbanksiana Lamb.), and black spruce (Piceamariana (Mill.) B.S.P.) using six upper diameter locations. The optimal location of the upper diameter was found to be 50% of the total height for red pine and white pine and 47% of total height for jack pine and black spruce. Product form is redefined as P = d* × H where d* = diameter-outside-bark at that average relative height on the tree where d* = (2 × V)/(D × H) as determined from a small sample of scaled trees, for each species and H = total height of tree.

Root-rotting fungi associated with mortality of conifer saplings in northern Ontario

1978 ◽  
Vol 8 (1) ◽  
pp. 17-22 ◽  
Author(s):  
Roy D. Whitney ◽  
Donald T. Myren
Keyword(s):  
Boreal Forest ◽  
Cause Of Death ◽  
Root Rot ◽  
Black Spruce ◽  
Red Pine ◽  
Balsam Fir ◽  
White Pine ◽  
Conifer Species ◽  
Northern Ontario

The roots of 435 dead or dying saplings, averaging 10 years of age, of seven conifer species from the Boreal Forest of northern Ontario were examined for root rot. Only trees with no obvious cause of death or decline, other than root rot, were selected. Eighty-three percent of the trees had root rot. Cultures revealed that Armillariamellea (Vahl ex Fr.) Kummer was associated with root rot in 68% of all trees examined, including more than 45% of the trees in each species. Ten other root-rotting fungi were isolated from 1% or fewer of the trees, 7 of them from balsam fir (Abiesbalsamea [L.] Mill.) and 3 from black spruce (Piceamariana [Mill.] B.S.P.). Scytinostromagalactinum (Fr.) Donk was isolated from sapwood of roots and lower stems of red pine (Pinusresinosa Ait.), balsam fir, white pine (P. strobes L.), and black spruce and appeared to be parasitic on these species. Coniophoraputeana (Schum. ex Fr.) Karst. was apparently associated with the death of one balsam fir.

USE OF THE RELATIVE TURGIDITY TECHNIQUE FOR MEASUREMENT OF WATER STRESSES IN GYMNOSPERM LEAVES

1965 ◽  
Vol 43 (2) ◽  
pp. 305-316 ◽  
Author(s):  
J. J. Clausen ◽  
T. T. Kozlowski
Keyword(s):  
Abies Balsamea ◽  
Pinus Resinosa ◽  
Tsuga Canadensis ◽  
Red Pine ◽  
Eastern Hemlock ◽  
Balsam Fir ◽  
White Pine ◽  
Sampling Variation

Adaptations of Weatherley's relative turgidity technique (Weatherley 1950), fitting it for use with red pine (Pinus resinosa Ait.), white pine (P. strobus L.), balsam fir (Abies balsamea (L.) Mill.), and eastern hemlock (Tsuga canadensis (L.) Carr.) are described. Results of preliminary investigations of sampling variation between trees, whorls, and needle ages in red pine are presented.

Microsite Soil Compaction Enhances Establishment of Direct-Seeded Jack Pine in Northwestern Ontario

1992 ◽  
Vol 9 (3) ◽  
pp. 107-112 ◽  
Author(s):  
Laird W. Van Damme ◽  
Lisa Buse ◽  
Steve Warrington
Keyword(s):  
Soil Compaction ◽  
Black Spruce ◽  
Mineral Soil ◽  
Sowing Date ◽  
Jack Pine ◽  
Early Spring ◽  
Northwestern Ontario ◽  
Direct Seeded ◽  
Treatment Responses ◽  
Sowing Season

Abstract The effects of microsite soil compaction on direct seeding of jack pine and black spruce were tested in conjunction with Bracke scarification. The compaction effect was achieved by manually tamping the seed spot. It was anticipated that compaction might decrease the number of seeds required to establish seedlings and extend the sowing season in Northwestern Ontario Experimental results showed that compaction increased the number of scalps stocked with jack pine by 30% after the first growing season. Compaction with a pyramidal surface doubled the percent stocked scalps over conventional sowing for the latest sowing date. Compaction may allow an extension of the jack pine sowing season from late June into early July. Still, early spring sowing provided the best overall results for both species. Compaction effects were not detected for black spruce. The experimental sowing rate of five seeds per scalp may have been insufficient to detect black spruce treatment responses on the dry mineral soil seed spots. North. J. Appl. For. 9(3):107-112.

Hand and Machine Tree Planting in Northern Ontario

1970 ◽  
Vol 46 (6) ◽  
pp. 477-478
Author(s):  
W. C. Stevens
Keyword(s):  
Black Spruce ◽  
Jack Pine ◽  
Tree Planting ◽  
White Pine ◽  
Northern Ontario ◽  
Rock Outcrops ◽  
Important Species ◽  
Precambrian Shield ◽  
Limited Scale ◽  
Commercial Forest

Northern Ontario lies entirely in the Precambrian Shield with its many rock outcrops, sand plains, valleys and extensive lowlands.Tree planting started on a limited scale in Northern Ontario in the 1920's but it was not until the mid-fifties that the program really expanded into millions of trees.White spruce, black spruce, jack pine, red pine and white pine are the most important species planted for commercial forest products.The advent of new site preparation techniques has made possible the planting of areas that were previously by-passed.Due to the rugged conditions in Northern Ontario, tree planting by machine is still not too prevalent.For the purpose of this paper, Northern Ontario is that portion of the province lying north of the historic fur-trading route of the French and Mattawa Rivers and the Great Lakes. The area is made up entirely of Precambrian shield with many outcrops of rock, sand plains of jack pine, valleys and extensive lowlands of spruce.

Estimating branch production in trembling aspen, Douglas-fir, jack pine, black spruce, and balsam fir

2007 ◽  
Vol 37 (6) ◽  
pp. 1024-1033 ◽  
Author(s):  
P.Y. Bernier ◽  
M.B. Lavigne ◽  
E.H. Hogg ◽  
J.A. Trofymow
Keyword(s):  
Primary Productivity ◽  
Net Primary Productivity ◽  
Black Spruce ◽  
Jack Pine ◽  
Douglas Fir ◽  
Balsam Fir ◽  
Trembling Aspen ◽  
Wood Production ◽  
Conifer Species ◽  
Branch Wood

Measuring net primary productivity of trees requires the measurement of total wood production of branches. Recent work on balsam fir ( Abies balsamea ) has shown that branch-wood production can be estimated as a function of foliage production. We extend the analysis to four other species found in the Canadian forest: black spruce ( Picea mariana ), jack pine ( Pinus banksiana ), Douglas-fir ( Pseudotsuga menziesii ), and trembling aspen ( Populus tremuloides ). Results show that the ratio of annual branch-wood production to annual foliage production is about 1.0 for conifer species (between 0.86 and 1.12) and 0.56 for aspen during a nondrought year. An analysis using field measurements of litterfall and stem-diameter increment from selected forested sites shows that branch-wood production accounts for a smaller proportion of aboveground net primary productivity in trembling aspen (15%–20%) than in conifer species (25%). Also, litterfall capture of small branches (<1 cm diameter) accounts for only 33% of branch detritus production in conifers and 50% in trembling aspen. This study supports the use of an alternative method for estimating branch-wood production that reduces the potential bias in field estimates of net primary productivity.

Black spruce decline triggered by spruce budworm at the southern limit of lichen woodland in eastern Canada

2001 ◽  
Vol 31 (12) ◽  
pp. 2160-2172 ◽  
Author(s):  
Martin Simard ◽  
Serge Payette
Keyword(s):  
Black Spruce ◽  
Abies Balsamea ◽  
Spruce Budworm ◽  
Jack Pine ◽  
Growth Patterns ◽  
Balsam Fir ◽  
Eastern Canada ◽  
Southern Limit ◽  
Epiphytic Lichen ◽  
Spruce Decline

Black spruce (Picea mariana (Mill.) BSP) is the dominant tree species of the southernmost (48°N) lichen woodlands in eastern Canada. Most spruce trees in mature lichen woodlands appear to be declining, as shown by the massive invasion of the epiphytic lichen Bryoria on dead branches of dying trees. A dendroecological study was undertaken to identify the main causal factors of the decline. A decline index based on the abundance of Bryoria on spruce trees was used to distinguish healthy from damaged lichen–spruce woodlands and to select sampling sites for tree-ring measurements. Three conifer species (black spruce, balsam fir (Abies balsamea (L.) Mill.), and jack pine (Pinus banksiana Lamb.)) were sampled to compare their growth patterns in time and space. In the late 1970s and mid-1980s, black spruce and balsam fir experienced sharp and synchronous radial-growth reductions, a high frequency of incomplete and missing rings, and mass mortality likely caused by spruce budworm (Choristoneura fumiferana (Clem.)) defoliation. Jack pine, a non-host species, showed no such trend. Because black spruce layers were spared, lichen woodlands will eventually regenerate unless fire occurs in the following years. Black spruce decline can thus be considered as a normal stage in the natural dynamics of the southern lichen woodlands.

Growth intercept models for black spruce, jack pine and balsam fir in Quebec

2005 ◽  
Vol 81 (1) ◽  
pp. 104-113 ◽  
Author(s):  
Daniel Mailly ◽  
Mélanie Gaudreault
Keyword(s):  
Pinus Banksiana ◽  
Black Spruce ◽  
Abies Balsamea ◽  
Site Index ◽  
Jack Pine ◽  
Balsam Fir ◽  
Practical Significance ◽  
Interim Testing ◽  
Growth Intercept ◽  
Mean Square Errors

The objective of this study was to develop variable growth intercept models for coniferous species of major importance in Quebec using Nigh's (1997a) modelling technique. Eighty-three, 68, and 70 stem analysis plots of black spruce (Picea mariana [Mill.] BSP), jack pine (Pinus banksiana Lamb.) and balsam fir (Abies balsamea (L.) Mill) were used, respectively. The growth intercept models for black spruce were the most precise, followed by those for jack pine and finally by those for balsam fir, based on the root mean square errors. Results indicated that the accuracy of the models was good, relative to those previously published for other species in Canada. Interim testing of the models revealed a low mean error for all three species that may not be of practical significance for site index determination, although more data should be obtained to further test the models. Key words: balsam fir, black spruce, growth intercept, jack pine, model, nonlinear regression, site index

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