Seasonal changes in the caloric value of the leaves and twigs of Populus tremuloides

1978 ◽  
Vol 56 (15) ◽  
pp. 1804-1805 ◽  
Author(s):  
T. D. W. James ◽  
D. W. Smith

Seasonally averaged caloric values (kilocalories per gram dry weight) of Populus tremuloides Michx. (trembling aspen) in southern Ontario were 5.17 for leaves, 5.04 for twig bark, and 4.55 for twig wood. The marked difference between leaves and twig wood reflects the differing composition of these tissues. The caloric levels of all the aspen components were highest in May. Levels decreased markedly from May to June, increased to a second peak in August, and then declined again between August and September. The caloric value of twig bark and wood also showed a decline from September to November. Seasonal fluctuations in caloric value of trembling aspen leaves and twigs were large compared with changes reported for other forest tree species and it is suggested that aspen is relatively sensitive to environmental effects.


1978 ◽  
Vol 56 (15) ◽  
pp. 1798-1803 ◽  
Author(s):  
T. D. W. James ◽  
D. W. Smith

Concentrations of N, P, K, Ca, and Mg were determined at monthly intervals over the growing season in the leaves, twig bark, and twig wood of Populus tremuloides Michx. (trembling aspen) and in the leaves and stems of Cornus stolonifera Michx. (red osier dogwood) in southern Ontario. Concentrations of N, P, and K in the leaves of both species decreased from May to August. Levels of Mg and Ca increased. Nutrient changes in aspen twigs during the May to September period, with the exception of magnesium, followed the reverse direction to those in the leaves. Seasonal changes in all of the nutrients in twigs were very small. Seasonal nutrient variability in red osier stems was also slight, but concentrations of Mg and Ca showed a July peak, and K showed a peak in June. N and P declined from early spring to midsummer but by September in dogwood the levels had returned to the April values.



2002 ◽  
Vol 80 (1) ◽  
pp. 93-100 ◽  
Author(s):  
L R Little

Plant competition is expected to produce an overdispersed spatial pattern relative to the initial pattern of individuals. The spatial patterns of two boreal forest tree species, Populus tremuloides Michx. (trembling aspen) and Pinus banksiana Lamb. (jack pine), were examined for evidence of intraspecific and interspecific competition. Data consisting of species, position, and age of tree stems were obtained from a 21-year-old, 40 m × 30 m postfire area of boreal forest in northern Alberta, Canada. Tree stems were mapped and classified according to size (greater or less than 5 cm in diameter at ground height) and species. A variation on the random mortality hypothesis was used to detect overdispersed patterns indicative of competitive interactions. This was done by comparing the size of neighbouring stems with those expected when the size or "success" of a stem occurred randomly. The results showed roughly two scales of pattern. First, large seed-regenerating jack pine neighboured each other more often than expected, but jack pine and trembling aspen neighboured each other less than expected. Second, although the large jack pine appeared to be clustered as neighbours, they tended to associate at distances farther than expected. These results show little evidence of density-dependence patterns in the species at the site, and the interspecific association between jack pine and trembling aspen could be indicative of a heterogeneous habitat.Key words: triangulation, size variability, Pinus banksiana, Populus tremuloides, jack pine, trembling aspen.



1935 ◽  
Vol 12 (6) ◽  
pp. 727-760 ◽  
Author(s):  
R. Darnley Gibbs

The chief species studied were paper birch, poplar (Populus tremuloides), jack pine, white spruce, and balsam fir.Methods for the study of water contents are described. Determinations of densities and swelling percentages are summarized. Conversion factors that may be employed to convert moisture contents based on dry weight into percentages of original volume are:—for jack pine 0.38, for balsam 0.315, for poplar 0.42 and for birch 0.49.The hardwoods examined show a maximum water content in spring and a sharp drop in the summer. This appears to vary from year to year and the possible reasons for this variation are discussed. In 1931 birch and poplar lost half their total (spring) water during the summer months. In birch this may not be made up until the following spring. The softwoods show no marked seasonal changes in water content.The distribution of water is characteristic for each species. Changes in distribution throughout the year have been followed. In birch all parts of the wood (there is no heartwood) join in the seasonal changes; in poplar only the sapwood varies in water content. The results of individual year-ring analyses and of borings at different heights point to uniform water content in corresponding parts of the tree.Diurnal changes in water content have been investigated and rapid fluctuations recorded. These point to a decrease during the morning followed by an increase later in the day. These variations are correlated with tension changes and no doubt also with transpiration. It seems certain that the actual amount of gas in the tree varies but little during the diurnal changes, though it does vary with the seasonal fluctuations in water content.Girdling of birch, balsam and spruce is described and the effects on water contents are followed. It is shown that in the case of birch, removal of wood to a depth of more than one inch leads to little change during two seasons. This is correlated with the continued activity of all parts of the wood. In balsam, almost complete drying of the sapwood within two or three months follows girdling through the sapwood. The characteristic wet patches of balsam heartwood, however, are unaffected, and it is concluded that these have no connection with the sapwood and so play no part in water conduction. The results from spruce are irregular.Experiments on seasoning and flotation in the field and in the laboratory are described. The summer seasoning of "sour-felled" birch is more rapid than that of normal or of peeled logs or the normal water loss of living standing trees, and this must be due to evaporation from the leaves.The effects of log length, of barking, and of end and/or side painting on rate of penetration of water have been investigated. While penetration of water is chiefly through the ends of logs, escape of dissolved air is largely in the radial direction, and so end penetration is less important than might be expected. There is considerable top drying from unseasoned floating logs (in laboratory tanks), which may assist in solution and removal of air and so hasten rather than slow up sinkage of the log. Seasoning followed by end painting results in very slow entry of water and so is excellent in flotation.



1998 ◽  
Vol 37 (6-7) ◽  
pp. 395-402
Author(s):  
Guus C. Stefess

A full-scale (470 m3) process for biological treatment of dredging spoil from the Petroleum Harbour in Amsterdam has been monitored during a pilot project. The dredging spoil was heavily polluted with polycyclic aromatic hydrocarbons (PAH) and mineral oil. The remediation chain involved dredging, transport of dredged spoil, hydrocyclone separation, froth flotation of the coarse particles, and biological treatment of the silt fraction (<20 μm) in stirred bioractors. The independent monitoring was aimed at recording the environmental effects, product quality and performance of the biological process. Hydrocyclone separation (cut point 20 m) resulted in two bulk streams: 65% sand and 30% silt (based on total dry weight of the input). The sand was cleaned and could be reused as building material. PAH and mineral oil were successfully concentrated in the silt fraction (<20 μm), which was treated biologically. Biological treatment during continuous feeding of fine fraction, at a residence time of 8-10 days for the entire bioreactor system, resulted in considerably reduced mineral oil and PAH contents. Furthermore, the leaching of organic contaminants was reduced, as well as the ecotoxicity. The obtained silt product however did not meet the demands, and had to be landfilled. Minor emissions of contaminants were measured in wastewater and offgas. The energy and chemicals consumption were acceptable. The biological process appears to be promising for the treatment of less-severely contaminated dredged material.



2021 ◽  
Vol 21 (1) ◽  
Author(s):  
Xiangfeng Tan ◽  
Mengmeng Liu ◽  
Ning Du ◽  
Janusz J. Zwiazek

Abstract Background Root hypoxia has detrimental effects on physiological processes and growth in most plants. The effects of hypoxia can be partly alleviated by ethylene. However, the tolerance mechanisms contributing to the ethylene-mediated hypoxia tolerance in plants remain poorly understood. Results In this study, we examined the effects of root hypoxia and exogenous ethylene treatments on leaf gas exchange, root hydraulic conductance, and the expression levels of several aquaporins of the plasma membrane intrinsic protein group (PIP) in trembling aspen (Populus tremuloides) seedlings. Ethylene enhanced net photosynthetic rates, transpiration rates, and root hydraulic conductance in hypoxic plants. Of the two subgroups of PIPs (PIP1 and PIP2), the protein abundance of PIP2s and the transcript abundance of PIP2;4 and PIP2;5 were higher in ethylene-treated trembling aspen roots compared with non-treated roots under hypoxia. The increases in the expression levels of these aquaporins could potentially facilitate root water transport. The enhanced root water transport by ethylene was likely responsible for the increase in leaf gas exchange of the hypoxic plants. Conclusions Exogenous ethylene enhanced root water transport and the expression levels of PIP2;4 and PIP2;5 in hypoxic roots of trembling aspen. The results suggest that ethylene facilitates the aquaporin-mediated water transport in plants exposed to root hypoxia.



1973 ◽  
Vol 51 (2) ◽  
pp. 498-500 ◽  
Author(s):  
Donald M. Knutson

Bacteria (Erwinia, Bacillus) were consistently isolated from all samples of aspen sapwood and heartwood. In wetwood zones (water-soaked xylem tissue) or discolored heartwood, large populations often occur. No organisms unique to wetwood were isolated. Wetwood probably is formed by nonmicrobial means and, once formed, merely supports large populations of indigenous bacteria.



2004 ◽  
Vol 82 (3) ◽  
pp. 310-315 ◽  
Author(s):  
Erin C Fraser ◽  
Victor J Lieffers ◽  
Simon M Landhäusser

In early May, 1-m sections of trembling aspen (Populus tremuloides Michx.) roots in a forest cutblock were carefully exposed and examined for damage. Undamaged roots were subjected to one of three wounding treatments (scrape, sever, or uninjured control) and were then reburied to either the full normal organic layer depth or to one third of the normal depth. Following one growing season, the roots were reexposed and assessed for aspen sucker numbers and growth rates. Results indicate that injured roots produced suckers nearly twice as often as uninjured roots. Further, injured roots produced more suckers per root, and these suckers were taller and had greater leaf area. Roots buried under shallow organic layers also generated more suckers, regardless of injury type. The side of injury (distal or proximal) did not affect any of the measured variables. The present study suggests that moderate wounding of aspen roots increases initial sucker numbers and growth rates.Key words: trembling aspen, root sucker, root injury, regeneration.



IAWA Journal ◽  
2002 ◽  
Vol 23 (2) ◽  
pp. 201-211 ◽  
Author(s):  
Simon Ellis ◽  
Paul Steiner

Five wood species, Oregon ash (Fraxinus latifolia Benth.), Balau (Shorea spp.), Douglas-fir (Pseudotsuga menziesii (Mirb.) Franco), Western red cedar (Thuja plicata Donn ex D. Don), and Trembling aspen (Populus tremuloides Michx.) were loaded in compression longitudinally, radially and tangentially. The wood cubes were conditioned to one of four moisture contents prior to loading. Small cubes were loaded until no void space remained after which samples were released and soaked in water. Stress /strain curves were recorded over the whole range of strain and cube thicknesses were recorded at the end of the compression, after release from the testing apparatus, and after soaking in water. Denser woods resulted in a greater Young’s modulus, higher levels of stress and shorter time to densification than did less dense woods. Higher initial moisture contents apparently increased the plasticity of the wood leading to a lower Young’s modulus and lower levels of stress during compression, greater springback after release of stress and greater recovery after swelling in water. Differences observed in the radial and tangential behaviours were believed to be due to the supporting action of the rays when the wood was compressed in the radial direction in balau and trembling aspen and to the relative difference between the lower density earlywood and higher density latewood regions in ash, Douglas-fir and western red cedar.



1993 ◽  
Vol 71 (1) ◽  
pp. 76-82 ◽  
Author(s):  
David L. Gibo ◽  
Jody A. McCurdy

The migration of Danaus plexippus during the late summer in southern Ontario in 1986 lasted for about 8 weeks and consisted of three phases, an early phase characterized by increasing abundance, a middle phase of peak abundance, and a late phase characterized by declining abundance. As the season progressed, systematic changes were observed in wet mass, dry mass, lean dry mass, lipid mass, and forewing length. Wet mass, lean dry mass, and forewing length were similar for early- and middle-phase individuals, but declined in late-phase migrants. Lipid mass peaked in the middle phase of the migration and then declined abruptly in the late phase. Dry mass also peaked in the middle phase, reflecting changes in lipid mass and lean dry mass. We hypothesize that the observed changes in lipid mass and lean dry mass over the 8 weeks resulted from changes in population structure as well as seasonal changes in the weather, and in availability of nectar. Opposing conclusions reached in previous studies of lipid accumulation in D. plexippus are probably the result of failure to control for phase of migration.



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