Leaf biomass changes with stand development in hinoki cypress (<Emphasis Type="Italic">Chamaecyparis obtusa</Emphasis> [Sieb. et Zucc.] Endl.)

We monitored a permanent plot of 3-year-old Chamaecyparis obtusa seedlings for 11 years after planting. As the stem cross-sectional area at the crown base can be regarded as a good predictor of leaf mass according to the pipe model theory, we measured this parameter to determine temporal trends in leaf biomass. The mean values showed asymptotic growth, maintaining a near-constant level after a stand age of 9 years. Peak values were found at 9 years, followed by a slight decrease because of a continuous reduction in stand density. This temporal trend suggests that the leaf biomass per unit land area attains a peak at an age of 9 years. As the stand density changes with stand age, the relationship between stand stem cross-sectional area at the crown base and stand density showed an optimum curve in which the optimum density was around 9200 ha⁻¹. We propose hypothetical trends in primary productivity and biomass density with stand age, based on the results of measurements of stem cross-sectional area at the crown base and stand density under the assumption of the 3/2 power law of self-thinning.     

Species-specific allometric scaling under self-thinning: evidence from long-term plots in forest stands

Experimental plots covering a 120 years' observation period in unthinned, even-aged pure stands of common beech (Fagus sylvatica), Norway spruce (Picea abies), Scots pine (Pinus sylvestris), and common oak (Quercus Petraea) are used to scrutinize Reineke's (1933) empirically derived stand density rule [see text], N=tree number per unit area, [see text]=mean stem diameter), Yoda's (1963) self-thinning law based on Euclidian geometry ([see text] [see text]=mean biomass per tree), and basic assumptions of West, Brown and Enquist's (1997, 1999) fractal scaling rules ([see text] [see text] w=biomass per tree, d=stem diameter). RMA and OLS regression provides observed allometric exponents, which are tested against the exponents, expected by the considered rules. Hope for a consistent scaling law fades away, as observed exponents significantly correspond with the considered rules only in a minority of cases: (1) exponent r of [see text] varies around Reineke's constant -1.605, but is significantly different from r=-2, supposed by Euclidian or fractal scaling, (2) Exponent c of the self-thinning line [see text] roams roughly about the Euclidian scaling constant -3/2, (3) Exponent a of [see text] tends to follow fractal scaling 8/3. The unique dataset's evaluation displays that (4) scaling exponents and their oscillation are species-specific, (5) Euclidian scaling of one relation and fractal scaling of another are coupled, depending on species. Ecological implications of the results in respect to self-tolerance (common oak>Norway spruce>Scots pine>common beech) and efficiency of space occupation (common beech>Scots pine>Norway spruce>common oak) are stressed and severe consequences for assessing, regulating and scheduling stand density are discussed.     

Linking stand-level self-thinning allometry to the tree-level leaf biomass allometry

Long-term experimental plots of Norway spruce and European beech are investigated for a link between stand-level self-thinning and tree-level leaf biomass allometry. Self-thinning refers to the finding of Reineke (1933), who postulated for unthinned forest stands that with β = −1.605; i.e. an increase of mean (quadratic) diameter d _q by 1% results in a decrease of tree number N by 1.605%. On the individual tree level, leaf biomass (w _L) can be related allometrically to the tree diameter d: w _L = ad ^α. If we assume that (a) the stands have reached the ceiling leaf area, (b) the specific leaf area (leaf area/leaf weight) is constant, and (c) differences resulting from the use of mean quadratic diameter or individual tree diameter are negligible, then the decrease in the stands’ leaf biomass due to the trees lost in self-thinning must be compensated by an equivalent increase in the remaining trees’ leaf biomass. This means, the absolute slope of the individual trees’ leaf biomass allometry α and the self-thinning allometry β would be equal and just have the opposite sign: α = −β. The analysis of the two long-term plots reveals that α is stronger than β, both for spruce (β = −1.744, α = 1.840) and especially for beech (β = −1.791, α = 2.181). The cause is traced back to a changing average specific leaf area during stand development [assumption (b) is wrong]. The results do not only bridge a gap between tree and stand allometry, but also emphasize an important effect for the understanding and modelling of the resource allocations in trees and forests.     

How to measure stand density

Foresters have produced many measures of stand density. Yet, none of these is entirely satisfactory. A majority of the measures (stand density index, basal area, and leaf area) present number of trees per unit area as a function of one factor: average tree size. This paper identifies the second factor driving self-thinning: the accumulation of gaps between tree crowns inevitable even in dense stands with a sizeable overlap of crowns. A model accounting for both factors allows us to quantify stand density and find a single number characterizing the density of undisturbed stands. The number changes with species, being higher for more shade tolerant ones. It is found that the second factor affects survival of trees but not their growth. This means that there are two kinds of stand density.     

Allometric relationships for Eucalyptus nitens (Deane and Maiden) Maiden plantations

Allometric relationships between stem, leaf area and crown dimensions were determined for Eucalyptus nitens (Deane and Maiden) Maiden using 81 trees sampled from 13 post-canopy closure sites and 34 trees sampled from 6 pre-canopy closure sites. These sites differed in site quality, stand age, fertiliser treatment, stand density and levels of weed infestation. Overall, tree age ranged from 2 to 13 years, tree height from 1.4 to 26.1 m and diameter at breast height from 0.6 to 38.7 cm. Pre-canopy closure trees exhibited site-specific relationships which were to some extent confounded with tree age. However, post-canopy closure trees had relationships which were independent of site, age and silvicultural treatments. Strong relationships between structural components were found for both stem and crown. Stem diameter at breast height was non-linearly related to tree height and crown length. Stem sapwood area (breast height or crown base) could be predicted from stem cross-sectional area. For post-canopy closure trees, a functional relationship between sapwood area (breast height and crown base) and leaf area was site-independent. The lack of specificity in terms of both site and management techniques enables these relationships to be applied generally to E. nitens plantations in Tasmania.     

Density effect, self-thinning and size distribution in Pinus densiflora Sieb. et Zucc. stands

The competition-density (C-D) effect for given times and self-thinning over time in even-aged, natural, pure stands of Pinus densiflora Sieb. et Zucc. were analyzed with the reciprocal equation of the C-D effect in self-thinning stands, and the equation describing the time-trajectory of mean stem volume and stand density. The C-D effect and self-thinning were consistently well explained by the two equations. Differences in mean stem volume and in stand density among the stands tended to merge with increasing stand age. The self-thinning line with a slope of approximately –3/2 was reached by the higher density stand prior to the medium and lower density stands. The skewness of tree height distribution showed positive values, which means that the distribution is more or less L-shaped, and in addition the skewness decreased with increasing mean tree height, which indicates that smaller trees died as the stands grew. This trend is consistent with the asymmetric (one-sided) competition hypothesis that self-thinning is driven by competition for light. The tree height distribution was analyzed using the Weibull distribution. The location parameter h _min of the Weibull distribution increased with increasing stand age, and the scale parameter a tended to increase slightly with increasing stand age. The range of the shape parameter b of the Weibull distribution corresponded to that of the skewness.     

Theoretical Relationships Between Mean Plant Size, Size Distribution and Self Thinning under One-sided Competition

As yet there is no comprehensive theory in plant populationecology to explain relationships between mean plant size, sizedistribution and self-thinning. In this paper, a new synthesisof plant monocultures is proposed. If the reciprocal relationshipbetween plant biomass and plant population density among variousstands of even-aged plant populations holds, the same reciprocalrelationship must exist between cumulative mass and cumulativenumber of plants from the largest individual within a population,assuming strict one-sided competition (which is an extreme conditionfor competition for light among plants). The two parametersof the relationship between cumulative mass and cumulative numberwithin a stand both correlate with maximum plant height in thestand. One parameter equals the reciprocal of the potentialmaximum plant mass per area, which is expressed by the productof maximum plant height and dry-matter density. The other parametercorrelates with the potential maximum individual plant mass,which is allometrically related to maximum plant height. Asa stand develops, the growth rate of the smallest individualswill become zero due to suppression from larger individuals,and they will die; i.e. self-thinning will occur. The slopeof the self-thinning line is expressed through the coefficientsof allometry between height and mass and between dry matterdensity and height. When the former coefficient is 3 and thelatter is 0, the gradient exactly corresponds to the value expectedfrom the 3/2 power rule, but it can take various values dependingon the values of the two coefficients. Competition among individualsdetermines size-density relationships among stands, which inturn determine the size structure of the stand. The size structureconstrains the growth of individuals and results in self-thinningwithin the stand.Copyright 1999 Annals of Botany Company. Monoculture, plant population, self-thinning, competition, hierarchy, size-structure.     

Branch surface area and its vertical distribution in coastal Douglas-fir

Wood area index (WAI; total surface area of branches and bole per unit of land area) is an important yet often neglected forest structural attribute. Branchwood surface area, in particular, has significant implications for many ecophysiological processes including total respiration and interception of radiation and rainfall. Branch surface area was estimated at the branch-, tree-, and stand-level for 33 Douglas-fir (Pseduotsuga menziesii [Mirb.] Franco) plantations in the Oregon Coast Range. Patterns in WAI, leaf area index (LAI; total surface area of needles per unit of land area), tree area index (TAI=WAI+LAI) and various ratios of these dimensions were then investigated. The main axes of primary branches (those attached to the main stem) comprised 82±13% of total branchwood surface area. Tree surface area (needles + woody tissue) increased with increasing tree size and crown length, and decreased with greater intensity of Swiss needle cast (SNC). At the stand-level, woody surface area increased with greater stand density and decreased with more severe SNC, but on average it constituted 29±12% of total tree surface area. Branchwood surface area and bole surface area contributed equally to WAI. The variation in WAI for a given LAI has important implications for radiation and rainfall attenuation in these stands and for accurate partitioning of intercepted radiation between photosynthetic and non-photosynthetic tissues.     

Effects of age and site quality on the distribution of biomass in Scots pine (Pinus sylvestris L.)

The distribution of the above-ground and below-ground biomass of Scots pine in southern Finland were investigated in trees of different ages (18–212 years) from two types of growth site. Secondly, some structural regularities were tested for their independence of age and growth site. Trees were sampled from dominant trees which could be expected to have a comparable position in stands of all ages. All stands were on sorted sediments. The biomass of the sample trees (18 trees) was divided into needles, branch sapwood and heartwood, stem sapwood and heartwood, stem bark, stump, large roots (diameter >20 cm), coarse roots (five classes) and fine roots. The amount of sapwood and heartwood was also estimated from the below-ground compartments. Trees on both types of growth site followed the same pattern of development of the relative shares of biomass compartments, although the growth rates were faster on the more fertile site. The relative amount of sapwood peaked after canopy closure, coinciding with the start of considerable heartwood accumulation. The relative amount of needles and fine roots decreased with age. The same was true of branches but to a lesser degree. The relative share of the below-ground section was independent of tree age. Foliage biomass and sapwood cross-sectional area were linearly correlated, but there were differences between the growth sites. Needle biomass was linearly correlated with crown surface area. The fine root to foliage biomass ratio showed an increasing trend with tree age.     

Stand and self-thinning dynamics in natural <Emphasis Type="Italic">Abies</Emphasis> stands in northern Hokkaido,Japan

Stand dynamics and self-thinning were analyzed in relation to the dynamics of above-ground biomass in natural Abies sachalinensis stands growing on sand dunes in northern Hokkaido, Japan. This was done in order to examine wave-type regeneration in the stands. Fifty-two plots were established in almost pure Abies stands that ranged from saplings to the mature and collapsing growth stages. Above-ground biomass and tree height reached asymptotic levels prior to the collapsing phase, unlike wave-regeneration Abies stands in central Japan and North America. Stand density was high in the young growth stages, but the self-thinning rate, that is, the density decrease per biomass growth in the study stands was greater than in wave-regeneration stands in central Japan, as indicated by a large self-thinning exponent (–1.26 by reduced major axis regression). The range of tree height distribution was very narrow, and the stands vertical structure was typically single-layered. The slenderness ratio of trees was large, except in young stands. In mature and collapsing stands, advanced seedling density increased markedly. These stand and tree characteristics were considered to be correlated with the wave-type regeneration in the study stands, and it is assumed that prevailing winds affect tree mortality.     

异速生长法计算秋茄红树林生物量

采用异速生长方法,建立树干基部多分枝型秋茄生物量与分枝直径的函数模型,根据该模型计算了浙江鳌江河口人工秋茄林生物量,并比较了我国不同地区秋茄林生物量差异。结果表明,秋茄生物量(W)与分枝直径(D)之间存在极显著的回归关系,叶片(WL)、树干(WS)、根系和分枝基部(WB)及植株总生物量(WT)与分枝直径(D)的异速生长方程分别为:WL=0.187D1.855(R2=0.612,P<0.0001);WS=0.267D1.906(R2=0.821,P<0.0001);WB=4.6D1.136(R2=0.644,P<0.0001);WT=3.614D1.446(R2=0.801,P<0.0001)。我国不同地区秋茄林地上生物量与林龄和纬度之间存在显著的回归关系:lg(地上生物量)=3.123+0.84×lg(林龄)-2.019×lg(纬度),(R2=0.431,F2,11=4.161,P=0.045)。秋茄种群生物量随着林龄的增加而增加,随着纬度的升高呈现降低趋势。浙江鳌江河口3年、5年和10年龄人工秋茄林生物量分别为7.13、11.32和24.35 t/hm2,其中5年龄秋茄林生物量仅为广东湛江同龄秋茄林(自然湿地生境)生物量的18%。然而,广东深圳的3年龄秋茄林(人工湿地生境)生物量仅为该研究中同龄秋茄林生物量的9.3%。此外,以≤11年龄的人工秋茄纯林为对象,建立了种群密度与种群植株平均生物量的关系:lg(平均单株地上生物量)=8.468-2.1×lg(种群密度),(R2=0.961,F=99.764,P=0.001),秋茄种群密度越小,平均植株生物量越大,平均单株生物量较符合Yoda提出的-3/2自疏定律为快,自疏指数为-2.1。因此,纬度和林龄是秋茄种群生物量的主要影响因子,生境类型、种群密度等因素对红树林种群或群落生物量的积累也至关重要。     

Estimating tree and stand sapwood area in spatially heterogeneous southeastern Australian forests

Aims Natural and anthropogenic changes in forests can have important influences on transpiration and water production. Understanding the effects of increasing disturbances, due for example to climate change and forest harvesting, requires detailed information on how forest density and structural attributes relate to transpiration. Mean annual transpiration of eucalypt forest communities is often strongly correlated with total cross-sectional sapwood area. Our aim was to test an efficient method for estimating sapwood area at 1.3 m height (SA 1.3) in a large number of trees to understand the spatial heterogeneity of tree and stand sapwood area within and between forest communities, and develop allometric relationships that predict SA 1.3 with forest inventory data. We also apply tree competition models to determine the degree to which the relationship between SA 1.3 and tree basal area at 1.3 m height (BA 1.3) is influenced by competition.Methods We visited 25 recently harvested southeastern Australian forest sites consisting of 1379 trees and 5 Eucalyptus species to evaluate a new efficient data collection method for estimating SA 1.3 with tree taper and stump dimensions data using mixed effects models. The locations of 784 stumps within one 5-ha site were accurately mapped using an unmanned aerial vehicle (UAV), and four distance-dependent tree competition models were applied across the site to explain within-stand variation in the ratio of SA 1.3 to BA 1.3. Data from 24 additional sites, consisting of ten 15 m radial plots per site, were used to analyse within-site variation in R Ha (the ratio of stand sapwood area SA Ha to stand basal area BA Ha). The radial plots were merged within each site to evaluate between-site variations in R Ha across the landscape. For predicting SA Ha with forest inventory data, we computed the relationship between SA Ha and a new index of total stem perimeter per hectare, defined as ? B A H a N T, where N T is tree stocking density.Important findings Our 1379 measured stems represent the most comprehensive measure of sapwood area, surpassing the 757 measured stems in native eucalypt forests published in literature. The species-specific R Ha varied considerably across sites and therefore extrapolating SA Ha with spatially distributed BA Ha maps and a generalized R Ha would introduce local uncertainty. We found that the species-specific stem perimeter index was more effective at capturing variability in SA Ha across the landscape using forest composition, structure and density data (R 2 : 0.72–0.77). The strong correlation between tree SA 1.3 and BA 1.3 improved slightly using tree competition models (R 2 increased from 0.86 to 0.88). Relating SA Ha to routinely measured forest inventory attributes within permanent plots and Light Detection and Ranging (LiDAR) data may provide opportunities to map forest water use in time and space across large areas disturbed by wildfire and logging.     

林木分化对兴安落叶松异速生长方程和生物量分配的影响

林木因对资源竞争而产生分化,从而影响林木的异速生长方程和生物量分配,但其影响程度还不清楚。采用林木相对直径法将38株兴安落叶松(Larix gmelinii)样木在林分中的分化等级分为优势木、中等木和被压木,量化林木分化对林木异速生长方程和生物量分配的影响。结果显示:生物量组分异速生长方程多以胸径(DBH)为自变量为好,但以枝下高处的树干直径为自变量估测其枝、叶生物量时更精确。在一定的胸径范围内,同一胸径下不同林木分化等级的地下部分各组分生物量没有显著差异(P0.05),但优势木分配更多的生物量给枝和叶,中等木比优势木分配更多的生物量给树干,中等木比被压木分配更多的生物量给地上部分,而且被压木和中等木的树高显著高于优势木。除根茎生物量之外,不同林木分化等级的生物量组分(包括枝、叶、树干和根系)的相对分配比例无显著差异(P0.05),根冠比保持相对稳定。这些结果表明,主要由竞争而引起的林木分化改变了兴安落叶松地上生物量组分的异速生长和分配,但其相对分配格局较为保守。     

Allometry and biomass of Korean pine (Pinus koraiensis) in central Korea

Aboveground tree biomass of Korean pine (Pinus koraiensis Sieb. et Zucc.) was determined for a natural forest of Korean pine and mixed deciduous trees and seven age classes of plantation forests in central Korea. Regression analyses of the dry weights of stem wood, stem bark, branches, and needles versus diameter at breast height were used to calculate regression equations of the form of log Y = a + b log X. Biomass of Korean pine in the mixed forest was 118 Mg ha(-1), and biomass in the plantations was linearly related to stand age, ranging from 52.3 Mg ha(-1) in 11 to 20-year-old stands to 317.9 Mg ha(-1) in 71 to 80-year-old stands. The proportions of stem wood and stem bark in the total aboveground biomass decreased with stand age while those of branch and needle increased. Specific leaf area of Korean pine ranging from 35.2 to 52.1 cm2 g(-1) was significantly different among crown positions and needle ages; in general, lower crown position and current needles had the greatest surface area per unit dry weight.     

Above- and below-ground characteristics associated with wind toppling in a young Populus plantation

 Damage from a dormant-season windstorm in a 3-year-old Populus research trial differed among four clones and three spacings and between monoclonal and polyclonal plots. Clonal differences in susceptibility to toppling (or leaning) were associated with both above- and below-ground characteristics. Susceptible clones had less taper in the lower stem and more weight in branches on the upper stem. The most susceptible clone also had the most above-ground biomass per unit of cross-sectional root area. The other susceptible clone had the least root system development in the windward quadrants. Wind toppling was least at the closest spacing. Apparently, mutual support was more important than individual tree characteristics from which the most damage would be expected at the closest spacing. Differences between paired trees of the same clone and spacing which did or did not topple were primarily associated with distribution of root systems by compass quadrant or depth. At the closest spacing where crown sway would have been minimized, trees which did not topple had greater cross-sectional root area in the windward direction than trees which did topple. At the widest spacing where crown sway would have been greatest, windfirm trees had greater cross-sectional root area than non-windfirm trees in both the windward and leeward directions. Toppling was reduced in polyclonal plots; this reduction may have been the result of more rapid stand differentiation in the polyclonal plots or reduction in the “domino effect” by inclusion of more windfirm clones in the mixture. Received: 23 October 1995 / Accepted: 22 February 1996     

An Individual Stand Growth Model for Mean Plant Size Based on the Rule of Self-thinning

A growth model for pure, even-aged stands of plants is asymptoticallybounded above by the self-thinning rule that relates maximumplant size to stand density. The model characterizes accretionin mean size as a deviation from the limiting size. It consistsof a function relating mean size to time and density and a companionsurvival model. The growth model is obtained by substitutingthe survival model for density in the mean size relationship.Model flexibility is demonstrated by fitting it to annual remeasurementsof mean size and number of plants per unit area in a stand ofPinus taeda L. 3/2-power rule, mortality, survival, stand dynamics, plant growth model, loblolly pine     

Revisiting a universal airborne light detection and ranging approach for tropical forest carbon mapping: scaling-up from tree to stand to landscape

Airborne laser scanning provides continuous coverage mapping of forest canopy height and thereby is a powerful tool to scale-up above-ground biomass (AGB) estimates from stand to landscape. A critical first step is the selection of the plot variables which can be related to light detection and ranging (LiDAR) statistics. A universal approach was previously proposed which combines local and regional estimates of basal area (BA) and wood density with LiDAR-derived canopy height to map carbon at a regional scale (Asner et al. in Oecologia 168:1147–1160, 2012). Here we explore the contribution of stem diameter distribution, specific wood density and height-diameter (H–D) allometry to forest stand AGB and propose an alternative model. By applying the new model to a large tropical forest data set we show that an appropriate choice of input variables is essential to minimize prediction error of stand AGB which will propagate at larger scale. Stem number (N) and average stem cross-sectional area should be used instead of BA when scaling from tree to plot. Stand quadratic mean diameter above the census threshold diameter size should be preferred over stand mean diameter as it reduces the prediction error of stand AGB by a factor of ten. Wood density should be weighted by stem volume per species instead of BA. LiDAR-derived statistics should prove useful for estimating local H-D allometries as well as mapping N and the mean quadratic diameter above 10 cm at the landscape level. Prior stratification into forest types is likely to improve both estimation procedures significantly and is considered the foremost current challenge.     

A model of physiological and allometric factors in the self-thinning curve

A generalized self-thinning curve for plants is derived from the modified Von Bertallanfy equation. When an asymptotic relation between photosynthesis per unit of leaf area and stocking density is assumed, the self-thinning curve thus derived is also asymptotic on a log-log scale but is fitted quite well by a log-linear approximation. The model predicts that the slope of the log-linear approximation is a function of (a) photosynthetic response to density and (b) the relation between leaf area and total aboveground biomass. Intercept of the log-linear approximation is a function of these plus maximum attainable biomass, site productivity, density at which maximum photosynthesis is attained, and the nature of carbon loss within the plant community. Linkages between various parameters within the model act to reduce differences in slope and intercept for species with different life history's and physiological requirements.     

The temporal response to drought in a Mediterranean evergreen tree: comparing a regional precipitation gradient and a throughfall exclusion experiment

Like many midlatitude ecosystems, Mediterranean forests will suffer longer and more intense droughts with the ongoing climate change. The responses to drought in long‐lived trees differ depending on the time scale considered, and short‐term responses are currently better understood than longer term acclimation. We assessed the temporal changes in trees facing a chronic reduction in water availability by comparing leaf‐scale physiological traits, branch‐scale hydraulic traits, and stand‐scale biomass partitioning in the evergreen Quercus ilex across a regional precipitation gradient (long‐term changes) and in a partial throughfall exclusion experiment (TEE, medium term changes). At the leaf scale, gas exchange, mass per unit area and nitrogen concentration showed homeostatic responses to drought as they did not change among the sites of the precipitation gradient or in the experimental treatments of the TEE. A similar homeostatic response was observed for the xylem vulnerability to cavitation at the branch scale. In contrast, the ratio of leaf area over sapwood area (LA/SA) in young branches exhibited a transient response to drought because it decreased in response to the TEE the first 4 years of treatment, but did not change among the sites of the gradient. At the stand scale, leaf area index (LAI) decreased, and the ratios of stem SA to LAI and of fine root area to LAI both increased in trees subjected to throughfall exclusion and from the wettest to the driest site of the gradient. Taken together, these results suggest that acclimation to chronic drought in long‐lived Q. ilex is mediated by changes in hydraulic allometry that shift progressively from low (branch) to high (stand) organizational levels, and act to maintain the leaf water potential within the range of xylem hydraulic function and leaf photosynthetic assimilation.     

Arbuscular mycorrhizal fungi alter plant allometry and biomass-density relationships

Background and Aims

Plant biomass–density relationships during self-thinning are determined mainly by allometry. Both allometry and biomass–density relationship have been shown to vary with abiotic conditions, but the effects of biotic interactions have not been investigated. Arbuscular mycorrhizal fungi (AMF) can promote plant growth and affect plant form. Here experiments were carried out to test whether AMF affect plant allometry and the self-thinning trajectory.

Methods

Two experiments were conducted on Medicago sativa L., a leguminous species known to be highly dependent on mycorrhiza. Two mycorrhizal levels were obtained by applying benomyl (low AMF) or not (high AMF). Experiment 1 investigated the effects of AMF on plant growth in the absence of competition. Experiment 2 was a factorial design with two mycorrhizal levels and two plant densities (6000 and 17 500 seeds m⁻²). Shoot biomass, root biomass and canopy radius were measured 30, 60, 90 and 120 d after sowing. The allometric relationships among these aspects of size were estimated by standardized major axis regression on log-transformed data.

Key Results

Shoot biomass in the absence of competition was lower under low AMF treatment. In self-thinning populations, the slope of the log (mean shoot biomass) vs. log density relationship was significantly steeper for the high AMF treatment (slope = –1·480) than for the low AMF treatment (–1·133). The canopy radius–biomass allometric exponents were not significantly affected by AMF level, but the root–shoot allometric exponent was higher in the low AMF treatment. With a high level of AMF, the biomass–density exponent can be predicted from the above-ground allometric model of self-thinning, while this was not the case when AMF were reduced by fungicide.

Conclusions

AMF affected the importance of below-ground relative to above-ground interactions and changed root vs. shoot allocation. This changed allometric allocation of biomass and altered the self-thinning trajectory.