• Refine Query
  • Source
  • Publication year
  • to
  • Language
  • 3
  • Tagged with
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • About
  • The Global ETD Search service is a free service for researchers to find electronic theses and dissertations. This service is provided by the Networked Digital Library of Theses and Dissertations.
    Our metadata is collected from universities around the world. If you manage a university/consortium/country archive and want to be added, details can be found on the NDLTD website.
1

Investigation into the productivity of single- and mixed-species, second-growth stands of western hemlock and western redcedar

Klinka, Karel, Collins, D. Bradley, Chourmouzis, Christine January 2001 (has links)
In BC, it is required that harvested areas be regenerated with a mixture of tree species whenever appropriate to the site. This policy is based upon the assumption that increases in stand productivity, reliability, and/or biodiversity can be achieved in mixed-species stands. However, the knowledge justifying this policy is at best incomplete. Differences in forest productivity of mixed-species stands have been attributed mostly to competition. However, an increasing number of studies are providing evidence to support alternate theories, in which positive plant interactions play a major role. Positive plant interactions are divided into two components: (i) competitive reduction through structural and physiological differences in above and below ground structures, and (ii) facilitation through any positive effect on the growing environment of one plant species by another. These theories have yet to be tested in forest ecosystems. The objectives of this study, with respect to naturally established, unmanaged, second-growth stands of western hemlock (Hw) (Tsuga heterophylla (Raf.) Sarg.), western redcedar (Cw) (Thuja plicata Donn ex D. Don in Lamb.), and their mixtures, were: (1) to review the mechanisms of positive plant interactions and their potential to occur in these mixtures, and (2) to compare the productivity of these three stand types, using relative and absolute yield.
2

The structure of single- and mixed-species, second-growth stands of Western hemlock and Western redcedar

Klinka, Karel, Varga, Pal, Montigny, Louise E. M. de, Chourmouzis, Christine January 2001 (has links)
The structure of a forest stand is characterized by: (a) species composition, (b) age, (c) size (diameter and height), and (d) spatial (horizontal and vertical) arrangement of the trees. Depending on the species, site, and disturbance history, the stand structure varies with time, thus providing a snapshot of a particular development stage. Research on growth and stand structure has shown that the spatial distribution of trees is one of the key determinants of stand productivity. Forest inventories and ecological surveys carried out in British Columbia (BC) have shown that the structure of naturally established, unmanaged stands varies from simple (single-species, single-storied, and even-aged) to complex (multi-species, multi-storied, and uneven-aged). Only a few studies have quantitatively characterized this range of structural complexity, with nearly all studies focusing on old-growth stands. BC forest policy requires that harvested areas be regenerated with a mixture of tree species whenever a mixture is suited to the site. This policy is based upon the assumption that under appropriate conditions, increases in stand productivity, reliability, and/or biodiversity can be attained in mixed-species stands. This assumption has not yet been tested for forest ecosystems. One mechanism by which different tree species can reduce crown competition for light is through vertical separation (the development of multiple canopy strata). Canopy stratification is not easily recognized in mixed-species stands, particularly when species have similar shade tolerance and height growth patterns, and no quantitative methods have been developed to detect stratification. The diameter frequency distribution of two-storied stands have been characterized by inverted J-shaped as well as modal curves. Although it would be more appropriate to characterize stand structure by height frequency distributions, these distributions have not been developed. We suggest that (i) a stand is stratified if there are distinct, quantitatifiable modes in the size distribution; either diameter, height, or crown height, and (ii) height or crown height distributions will be the most sensitive measures. To characterize the structure of western hemlock (Tsuga heterophylla (Raf.) Sarg.) (Hw) and western redcedar (Thuja plicata Donn ex D. Don in Lamb.) (Cw) second-growth stands, and to investigate its influence on tree growth, we (1) described and compared size (diameter, height, and crown height) frequency distributions in single- and mixed-species stands, (2) determined whether mixed-species stands develop a stratified canopy, and (3) examined whether interactions between hemlock and redcedar affect tree growth.
3

Forest floor nutrient properties in single- and mixed-species stands of Western hemlock and Western redcedar

Klinka, Karel, Collins, D. Bradley, Montigny, Louise E. M. de, Feller, M. C. (Michael Charles), Chourmouzis, Christine January 2001 (has links)
The influence of tree species on forest soils has been the subject of study for at least a century. Of particular interest have been western hemlock (Tsuga heterophylla (Raf.) Sarg.) and western redcedar (Thuja plicata Donn ex D. Don) – two of the most common tree species in coastal and southern British Columbia, but each with a different nutrient amplitude. It has generally been found that acid, mycogeneous Mor humus forms develop in hemlock stands, while less acid and more zoogenous Mormoder, Moder, or even Mull humus forms develop in redcedar stands. The objective of this study was to determine the influence of hemlock and redcedar, growing separately and together, on forest floor nutrient properties. The questions addressed were: (1) does each stand type have unique forest floor nutrient properties? and (2) can any forest floor nutrient property discriminate between stand types?

Page generated in 0.0789 seconds