Long-term response of planted conifers, natural regeneration, and vegetation to harvesting, scalping, and weeding on a boreal mixedwood site

This study reports 14th-year response of a boreal mixedwood stand to different harvest intensities (uncut, 50% partial cut with and without removal of residuals after 3 years, and clearcut), spot site preparation treatments (none and scalped), and chemical weeding frequencies (none, single, and multiple) in northeastern Ontario. The response variables include the survival and growth of planted white spruce (Picea glauca [Moench] Voss) and jack pine (Pinus banksiana Lamb.), height and density of natural regeneration and shrubs, and cover of shrubs and non-woody vegetation. Harvesting and weeding generally improved survival and growth of planted trees, although white spruce survival did not significantly differ among the three weeding frequencies. Harvesting tended to increase heights of hardwood (mostly trembling aspen (Populus tremuloides Michx.)) and conifer (largely balsam fir (Abies balsamea (L.) Mill.).) natural regeneration, cover and density of shrubs, and cover of herbs, lichens, and ferns. Chemical weeding reduced height, density and cover of shrubs, height and density of hardwood regeneration, and fern cover, but increased moss and lichen cover. Spot scalping did not significantly affect planted seedling, natural regeneration, or the vegetation.Maximum survival and growth of planted white spruce and jack pine were achieved using a combination of clearcutting and multiple weeding. However, partial cutting followed by a single weeding produced acceptable survival and reasonable growth of planted trees, particularly for white spruce. Partial canopy removal alone substantially reduced the amount of hardwood regeneration, relative to clearcutting, but did not adequately suppress understory shrubs. Significant improvement in seedling growth following multiple weedings was evident primarily in the complete canopy removal treatments: 50% partial cut with removal of residuals after 3 years and clearcut. While the effects of harvesting and weeding on planted crop trees found in the 5th-year assessments generally persisted at year 14, survival decreased, likely due to light competition from developing hardwood and shrubs.     

Facilitative and competitive effects of a N-fixing shrub on white fir saplings

In Sierra Nevada forests, shrubs are considered strong soil moisture competitors with regenerating trees, reducing seedling establishment, and slowing growth. Recent studies, however, suggest that in some circumstances shrubs can facilitate tree establishment and growth by modifying harsh microclimate conditions; increasing acquisition of water, carbon, and/or nutrients via shared mycorrhizal connections; or enhancing soil fertility, particularly under nitrogen-fixing shrubs such as Ceanothus spp. We examined the establishment dates and growth rates and patterns of white fir saplings growing in greenleaf manzanita, whitethorn ceanothus, and bare patches to examine whether establishment was correlated with past wet years, whether saplings growing in ceanothus had nitrogen-enriched foliage or faster growth rates than in the other two patches, and whether saplings in shrub patches experienced competition for light.Sapling establishment was not correlated with high precipitation or heavy snowpack years, suggesting shade-tolerant saplings do not need wet years to become established. Soils under ceanothus were nitrogen enriched, but white fir sapling foliage did not have higher nitrogen concentrations and saplings did not grow faster in ceanothus than in the other two patches. Because growth rates of saplings were comparable in all patch types examined despite significantly different edaphic and abiotic conditions, we inferred that the various competitive and facilitative interactions affecting tree growth are in net balance across the patch types examined. However, competition for light is important—a significant percentage of growth release events occurred after saplings emerged above their host shrubs. Where shrubs are present, shade-tolerant species (i.e., white fir) are favored over drought-tolerant (pine) species. Our results may help interpret changes in understory conditions that are contributing to mixed conifer's compositional shift toward more shade-tolerant species after a century of fire-suppression.     

Five-year radial growth of red oaks in mixed bottomland hardwood stands

We studied the relationships among 5-year radial (diameter and basal area) growth of red oak (genus Quercus, subgenus Erythrobalanus) crop trees and predictor variables representing individual tree vigor, distance-dependant competition measures, and distance-independent competition measures. The red oaks we examined are representative of the commercially and ecologically important oak species of the bottomland hardwood forests of the southeastern US. The crown class score, a quantitative measure of crown class and tree vigor, performed best in accounting for the variability in tree diameter growth. Plot-level variables failed to account for a significant proportion of the variability in tree radial growth. The basal area of the first-order neighbors that were taller than the crop trees and located within 2.4 times the mean overstory crown radius had the highest negative correlation with crop tree 5-year radial growth. Red oaks were a major part of these competitors and likely exerted the greatest competitive pressure. However, crop tree radial growth was positively associated with the basal area of the red oaks which were indirect (second order) neighbors and which were taller than the crop trees. It is possible that indirect neighbors do not compete with the crop trees, but they likely compete with the direct competitors of the crop trees, thus having an indirect positive influence on crop tree growth. Such reasoning is consistent with previously observed spatial dependence up to four times the mean overstory crown radius. The findings may have implications for thinning hardwoods stands and crop tree management in that foresters need to take into account (1) oak intra-genus competition, (2) the negative competitive effect of direct neighbors, and (3) the potentially positive effect of the indirect neighbors, the competitors’ competitors.     

Interactions amongst trees and crops in <Emphasis Type="Italic">taungya</Emphasis> systems of western Kenya

Lack of empirical data on the effects of the taungya system on establishment and early growth of softwood plantations have partly contributed to controversial decisions regarding the continued suitability of the system for plantation establishment in Kenya. This study examined effectiveness of taungya systems of forest plantation establishment using Cupressus lusitanica and Pinus patula trees with Zea mays (maize) as a test intercrop on two contrasting site types (deep and shallow soils) in Mt. Elgon forest, western Kenya . Four treatments were evaluated in each site: trees with or without weed control, trees intercropped with maize, and sole maize. Results showed that tree survival, growth and nutrient uptake, and maize growth and yield were higher in the deep soil site than the shallow site. The t aungya system improved tree survival and growth, effects being greater in the deep than the shallow soil site. Both Cupressus lusitanica and Pinus patula trees had the same effects on maize growth and yield, reducing maize growth by 41–48% in the deep soil sites, and by 16–26% in the shallow site. Vector nutrient analysis and vector competition analysis of the treatment effects on growth and nutrient uptake of the trees and the maize crop suggested competition for N on the deep soils, but competition for K and P on the shallow soils. The study has demonstrated the applicability of graphical vector competition analysis in diagnosing tree–crop interactions in agroforestry.     

Biophysical interactions in tropical agroforestry systems

The rate and extent to which biophysical resources are captured and utilized by the components of an agroforestry system are determined by the nature and intensity of interactions between the components. The net effect of these interactions is often determined by the influence of the tree component on the other component(s) and/or on the overall system, and is expressed in terms of such quantifiable responses as soil fertility changes, microclimate modification, resource (water, nutrients, and light) availability and utilization, pest and disease incidence, and allelopathy. The paper reviews such manifestations of biophysical interactions in major simultaneous (e.g., hedgerow intercropping and trees on croplands) and sequential (e.g., planted tree fallows) agroforestry systems. In hedgerow intercropping (HI), the hedge/crop interactions are dominated by soil fertility improvement and competition for growth resources. Higher crop yields in HI than in sole cropping are noted mostly in inherently fertile soils in humid and subhumid tropics, and are caused by large fertility improvement relative to the effects of competition. But, yield increases are rare in semiarid tropics and infertile acid soils because fertility improvement does not offset the large competitive effect of hedgerows with crops for water and/or nutrients. Whereas improved soil fertility and microclimate positively influence crop yields underneath the canopies of scattered trees in semiarid climates, intense shading caused by large, evergreen trees negatively affects the yields. Trees in boundary plantings compete with crops for above- and belowground resources, with belowground competition of trees often extending beyond their crown areas. The major biophysical interactions in improved planted fallows are improvement of soil nitrogen status and reduction of weeds in the fallow phase, and increased crop yields in the subsequent cropping phase. In such systems, the negative effects of competition and micro-climate modification are avoided in the absence of direct tree–crop interactions. Future research on biophysical interactions should concentrate on (1) exploiting the diversity that exists within and between species of trees, (2) determining interactions between systems at different spatial (farm and landscape) and temporal scales, (3) improving understanding of belowground interactions, (4) assessing the environmental implications of agroforestry, particularly in the humid tropics, and (5) devising management schedules for agroforestry components in order to maximize benefits. This revised version was published online in June 2006 with corrections to the Cover Date.     

Contributions of woody and herbaceous vegetation to tropical savanna ecosystem productivity: a quasi-global estimate

To estimate the relative contributions of woody and herbaceous vegetation to savanna productivity, we measured the 13C/12C isotopic ratios of leaves from trees, shrubs, grasses and the surface soil carbon pool for 22 savannas in Australia, Brazil and Ghana covering the full savanna spectrum ranging from almost pure grassland to closed woodlands on all three continents. All trees and shrubs sampled were of the C3 pathway and all grasses of the C4 pathway with the exception of Echinolaena inflexa (Poir.) Chase, a common C3 grass of the Brazilian cerrado. By comparing the carbon isotopic compositions of the plant and carbon pools, a simple model relating soil delta 13C to the relative abundances of trees + shrubs (woody plants) and grasses was developed. The model suggests that the relative proportions of a savanna ecosystem's total foliar projected cover attributable to grasses versus woody plants is a simple and reliable index of the relative contributions of grasses and woody plants to savanna net productivity. Model calibrations against woody tree canopy cover made it possible to estimate the proportion of savanna productivity in the major regions of the world attributable to trees + shrubs and grasses from ground-based observational maps of savanna woodiness. Overall, it was estimated that 59% of the net primary productivity (Np) of tropical savannas is attributable to C4 grasses, but that this proportion varies significantly within and between regions. The C4 grasses make their greatest relative contribution to savanna Np in the Neotropics, whereas in African regions, a greater proportion of savanna Np is attributable to woody plants. The relative contribution of C4 grasses in Australian savannas is intermediate between those in the Neotropics and Africa. These differences can be broadly ascribed to large scale differences in soil fertility and rainfall.     

美国目标树经营体系及其经营效果研究进展

目标树经营是一种通过降低邻木冠层竞争、增加目标树生长空间来提高单株木质量的营林技术, 可以看作是一种特殊的抚育间伐。文中从目标树选择标准、目标树密度、树冠重叠释放作业和作业时间等方面阐述了目标树经营体系, 并综述了目标树经营对单株目标树生长(直径、蓄积、树高、树冠)的影响和成本效益分析等研究进展, 以期为我国森林经营实践提供借鉴。     

Advances in modelling and decision support systems for vegetation management in young forest plantations

The two most common forest vegetation management objectivesare to (1) minimize resource competition, and (2) to developmethods for managing specific weed species. This paper reviewsrelevant models and decision support systems for assisting inachieving these objectives. The aim of reducing resource competitionis to increase crop-tree growth and survival. Several modellingapproaches have been applied to this problem and these generallyestimate crop survival and growth benefits following some formof generalized weed control. Linkages with models of older treecrops are needed for comparing vegetation management strategiesin the context of complete silvicultural regimes. More refinedindividual tree models use competition indices to estimate thequantity of weed vegetation within the growing space aroundeach tree. The indices reflect resource use by the weeds andare sensitive to changes in weed growth over time and to theapplication of specific vegetation management treatments. Hybridand process-based models have the potential to provide moregeneralized models of inter-specific competition, but theirusefulness for forest practitioners has yet to be proven. Someforest vegetation management problems require a more detailedunderstanding of the biology and ecology of a specific species.In this case, different modelling approaches that consider overallweed population dynamics, distribution or spread may be appropriate.     

Growth and yield of sorghum or cowpea in an agrisilviculture system in semiarid India

This study was conducted near Hyderabad, India during 1991–1994 to quantify the effects of shoot pruning, fertilization, and root barriers around Leucaena leucocephala trees on intercropped sorghum(Sorghum bicolor) or cowpea (Vigna unguiculata) crop production under rainfed conditions. Crop plants grown with pruned trees attained higher dry matter and leaf area index than did those with unpruned trees. Two-year mean grain yields of sorghum with no root barriers were76% and 39% of pure crop yield (1553 kg ha–1)for pruned and unpruned trees, respectively. Corresponding values for cowpea were 49% and 26% of pure crop yield (1075 kgha–1). Sorghum or cowpea intercropped with trees responded to fertilizer application more strongly than did their respective pure crops, suggesting an increased need for fertilizer application in this agrisilviculture system over that currently used for pure crops. Impact of root barriers was small on either crop. Irrespective of root barriers, a high response to tree pruning suggested above ground competition for light dominated tree/crop interactions in this agrisilviculture system. This revised version was published online in June 2006 with corrections to the Cover Date.     

滇东南岩溶地区植被结构优化造林模式研究

在岩溶地区采用墨西哥柏、川滇桤木、清香木、紫花苜蓿等16个树(草)种进行的12种配置模式试验表明:合理的乔灌草配置,有利于长短结合科学经营,前期牧草生长迅速,能很快覆盖地表,减少水土流失,并为牲畜提供大量的饲料,林木长大郁闭度增加后,牧草生长衰退,逐渐转向以经营林木为主。通过综合分析筛选出了适应性强、造林成活率高、生长旺盛、种间共生性良好的优化造林模式8种。     

A review of belowground interactions in agroforestry, focussing on mechanisms and management options

This review summarises current knowledge on root interactions in agroforestry systems, discussing cases from temperate and tropical ecosystems and drawing on experiences from natural plant communities where data from agroforestry systems are lacking. There is an inherent conflict in agroforestry between expected favourable effects of tree root systems, e.g. on soil fertility and nutrient cycling, and competition between tree and crop roots. Root management attempts to optimise root functions and to stimulate facilitative and complementary interactions. It makes use of the plasticity of root systems to respond to environmental factors, including other root systems, with altered growth and physiology. Root management tools include species selection, spacing, nutrient distribution, and shoot pruning, among others. Root distribution determines potential zones of root interactions in the soil, but are also a result of such interactions. Plants tend to avoid excessive root competition both at the root system level and at the single-root level by spatial segregation. As a consequence, associated plant species develop vertically stratified root systems under certain conditions, leading to complementarity in the use of soil resources. Parameters of root competitiveness, such as root length density, mycorrhization and flexibility in response to water and nutrient patches in the soil, have to be considered for predicting the outcome of interspecific root interactions. The patterns of root activity around individual plants differ between species; knowing these may help to avoid excessive competition and unproductive nutrient losses in agroforestry systems through suitable spacing and fertiliser placement. The possibility of alleviating root competition by supplying limiting growth factors is critically assessed. A wide range of physical, chemical and biological interactions occurs not only in spatial agroforestry, but also in rotational systems. In a final part, the reviewed information is applied to different types of agroforestry systems: associations of trees with annual crops; associations of trees with grasses or perennial fodder and cover crops; associations of different tree and shrub species; and improved fallows. This revised version was published online in June 2006 with corrections to the Cover Date.     

Driving competitive and facilitative interactions in oak dehesas through management practices

Dehesas are extant multi-purpose agroforestry systems that consist of a mosaic of widely-spaced scattered oaks (Quercus ilex L.) combined with crops, pasture or shrubs. We aimed to clarify the role of trees in dehesas of CW Spain focussed on the analysis of tree-understorey interactions. Spatial variability of resources (light, soil moisture and fertility), microclimate, fine roots of both herbaceous plants and trees and forage yield was measured. Additionally, we compared the nutritional and physiological status, growth and acorn production of oaks in cropped (fodder crop), grazed (native grasses) and encroached (woody understorey) dehesa plots. Significant light interception by trees was limited to the close vicinity of the trees, with very low reduction away from them. Both microclimate and soil fertility improved significantly in the trees vicinity, irrespective of soil management. Soil moisture varied very few with distance from the trees, as a result of the extended root system of oaks. Root systems of trees and herbs did not overlap to a great extent. Crop production was higher beneath trees than beyond the trees in unfertilised plots and foliar nutrient content of oaks did not increase significantly with crop fertilisation, indicating that trees and crops hardly compete for nutrients. Moreover, trees benefited from the crop or pasture management: trees featured a significantly improved nutritional and physiological status, a faster growth and a higher fruit productivity than trees growing in encroached or forest plots.     

Plant-soil interactions in multistrata agroforestry in the humid tropicsa

Multistrata agroforestry systems with tree crops comprise a variety of land use systems ranging from plantations of coffee, cacao or tea with shade trees to highly diversified homegardens and multi-storey tree gardens. Research on plant-soil interactions has concentrated on the former. Tree crop-based land use systems are more efficient in maintaining soil fertility than annual cropping systems. Certain tree crop plantations have remained productive for many decades, whereas homegardens have existed in the same place for centuries. However, cases of fertility decline under tree crops, including multistrata agroforestry systems, have also been reported, and research on the causal factors (both socioeconomic and biophysical) is needed. Plantation establishment is a critical phase, during which the tree crops require inputs but do not provide economic outputs. In larger plantations, tree crops are often established together with a leguminous cover crop, whereas in smallholder agriculture, the initial association with food crops and short-lived cash crops can have both socioeconomic and biological advantages. Fertilizers applied to, and financed by, such crops can help to `recapitalize' soil fertility and improve the development conditions of the young tree crops. Favorable effects on soil fertility and crop nutrition have been observed in associations of tree crops with N<sub>2</sub>-fixing legume trees, especially under N-deficient conditions. Depending on site conditions, the substitution of legume `service' trees with fast-growing timber trees may lead to problems of competition for nutrients and water, which may be alleviated through appropriate planting designs. The reduction of nutrient leaching and the recycling of subsoil nutrients are ways to increase the availability of nutrients in multistrata systems, and at the same time, reduce negative environmental impacts. These processes are optimized through fuller occupation of the soil volume by roots, allowing a limited amount of competition between associated species. The analysis of temporal and spatial patterns of water and nutrient availability within a system helps to optimize the use of soil resources, e.g., by showing where more plants can be added or fertilizer rates reduced. Important research topics in multistrata agroforestry include plantation establishment, plant arrangement and management for maximum complementarity of resource use in space and time, and the optimization of soil biological processes, such as soil organic matter build-up and the stabilization and improvement of soil structure by roots, fauna and microflora. This revised version was published online in June 2006 with corrections to the Cover Date.     

A split-root apparatus for examining the effects of hydraulic lift by trees on the water status of neighbouring crops

We describe a split-root system for examining the effects of hydraulic lift by trees on crop growth. In this system, upper lateral tree roots were grown in a container set on the ground through which the taproot of the tree could penetrate into the moist soil below. The container, with a radius of 0.5 m and a height of 0.20 m, consisted of two compartments divided by a waterproof barrier. A markhamia tree (Markhamia lutea (Benth.) Schumann) and upland rice (Oryza sativa (L.)) plants were planted in one compartment, with only rice plants planted in the other compartment. Irrigation of the container was ceased at the start of the experiment. The stomatal conductance of the rice plants in the associated side, in which both trees and rice plants were grown, declined more rapidly during the first drying period than in the rice-only compartment, suggesting that there was competition for water between the tree and the crop plants. However, during the later drying period, the rice plants in the associated side were green and viable, while those in the rice-only side became desiccated. Rice roots were seen intermingling with tree roots, and the soil water content in the associated site tended to be higher than in the rice-only side. It is likely that hydraulic lift occurred in the associated side and that water that had been transferred to the surface roots was released into the soil, enabling the rice plants in this compartment to remain viable. This novel system is useful for examination of the effects of hydraulic lift by trees on the growth of neighbouring crops. This revised version was published online in June 2006 with corrections to the Cover Date.     

Wildlife species associated with non-coniferous vegetation in Pacific Northwest conifer forests: A review

Non-coniferous vegetation, including herbs, shrubs, and broad-leaved trees, makes a vital contribution to ecosystem function and diversity in Pacific Northwest conifer forests. However, forest management has largely been indifferent or detrimental to shrubs and trees that have low commercial value, in spite of a paradigm shift towards more holistic management in recent decades. Forest management practices that are detrimental to broad-leaved trees and shrubs are likely to decrease habitat diversity for wildlife, but the number of species that may be affected has not previously been enumerated. I reviewed life history accounts for forest-dwelling vertebrate wildlife species and derived a list of 78 species in Oregon and Washington that are associated with non-coniferous vegetation. The diversity of direct and indirect food resources provided was the primary functional basis for associations of most species with non-coniferous vegetation. Thus, a diversity of herbs and broad-leaved trees and shrubs provides the foundation for food webs that contribute to diversity at multiple trophic levels in Pacific Northwest conifer forests. Given the number of species associated with non-coniferous vegetation in conifer-dominated forests, maintaining habitats that support diverse plant communities, particularly broad-leaved trees and shrubs, will be an important component of management strategies intended to foster biodiversity. Silvicultural practices such as modified planting densities, and pre-commercial and commercial thinning, can be used to control stand density in order to favor the development of understory herbs, shrubs, and a diversity of tree species within managed stands. Allowing shrubs and hardwood trees to develop and persist in early seral stands by curtailing vegetation control also would benefit many species associated with non-coniferous vegetation.     

The role of germination microsite in the establishment of sugar pine and Jeffrey pine seedlings

Mature shrubs can provide microhabitats that are beneficial to tree seedling growth and development. Sugar pine trees (Pinus lambertiana) grow in a narrow zone on the eastern slope of the Carson Range in extreme western Nevada, whereas Jeffrey pine (Pinus jeffreyi) is the dominant tree species in the region, an area extensively disturbed by wild fire. This study compares seedling establishment of sugar pine and Jeffrey pine relative to mature shrubs. In the fall of 2002 (cohort 1) and 2003 (cohort 2), 13,600 seeds of both species were planted in wire mesh enclosures, at three sites, under a variety of microhabitat treatments: under shade and in the open, under two species of shrub cover, and with and without plant litter. Seedlings were monitored for survival through two growing seasons. Even though more sugar pine seedlings emerged, more Jeffrey pine seedlings survived, and Jeffrey pine was the more drought tolerant species, better suited for the xeric climate found in the Carson Range. Litter slightly hindered seedling emergence but had no effect on survival and there was no significant species × litter interaction. Supplemental water facilitated survival in all treatments with highest survival in shade treatments. Sugar pine seedlings showed a significant increase in survival over Jeffrey pine seedlings with the addition of water, particularly in open treatments and more of both species survived under manzanita shrubs with water. The highest seedling mortality occurred when shrub canopy was removed, and seedlings experienced the effect of full sun and competition for soil water. For either species, microhabitat is a significant factor in determining success or failure in rehabilitation efforts after disturbance.     

Effects of understorey vegetation on tree establishment and growth in a silvopastoral system in northern Greece

The interaction between understorey plants and trees in a young silvopastoral system was studied in a sub-humid Mediterranean environment with cold winters in northern Greece. The experimental design was a split-split plot with three replications and included: three understorey treatments (grass, legume and control), two tree species (Acer pseudoplatanus and Pinus sylvestris) and two spacings (2.5×2.5 m and 3.5×3.5 m). The competition between herbaceous plants and trees resulted in significant differentiation in tree growth while their spacing did not produce any significant differences. The influence of trees on herbage yield either by plant species or spacing was not significant. During the early stages of establishment, a significant positive correlation was observed between sycamore growth and soil moisture, leaf weight, leaf area and leaf number as well as nitrogen and potassium concentration in leaves. Six years after planting the height increase of the sycamore trees was largest in the control treatment (415%), lowest in the grass treatment (134%) and intermediate (192%) in the legume treatment. Much higher was the increase obtained for the diameter, 161%, 207% and 536% respectively for the grass, legume and control treatments. The Scots pine trees grew faster than sycamore over the course of the experiment. Height increased by 397%, 351% and 400% and diameter by 518%, 443% and 683% respectively for the grass, legume and control treatments. This revised version was published online in June 2006 with corrections to the Cover Date.     

Maximizing crop yield in alley crops

A simple graphical model is presented illustrating the balance between facilitation and competition necessary for maximizing crop yield in alley cropping systems. Three functions are composed into the decision function: (1) the percent increase in crop yield from facilitation resulting from prunings, (2) the amount of prunings resulting from different tree densities, and (3) the percent reduction in crop yield from competition from trees. The resulting function illustrates how the balance between facilitation and competition may provide a window of opportunity for the beneficial use of alley crops. This revised version was published online in August 2006 with corrections to the Cover Date.     

Assessing components of a competition index to predict growth in an even-aged Pinus nigra stand

The relationship between tree growth and competition may depend on some subjective choices that are commonly left to the researcher. Among these are the neighborhood radius, the number of years of growth that are integrated, and tree age. We have evaluated the importance of these factors when relating growth and competition in a forest stand with contrasted densities of the dominant tree species (Pinus nigra) and understory shrub species (Adenocarpus decorticans). Previous to this evaluation we performed a randomization test to assess the relationship between tree growth and neighbors. By using Daniels index of competition we found that the use of a fixed neighborhood radius underestimated the importance of tree competition. The coefficient of determination (r²) of the relationship between tree growth and Daniels index increased asymptotically with the number of years considered. Five years of growth gave high r² independently of the density of trees and shrubs. The intensity of competition was weakly affected by the characteristics of the plot (tree and shrub densities), and did not change with time. In contrast, the potential growth at equal competition – as represented by constant a in the allometric model – changed with time suggesting a gradual decrease in potential tree growth in the plots with higher tree density, and a gradual increase in those plots with high density of shrubs. These results may reflect tree canopy closure and the senescence of Adenocarpus decorticans. A method is suggested to select optimum neighborhood radius and growing period for the calculation of competition indices. By applying this method we were able to explain as much as 79–84% of the variability in tree growth of this stand.