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.     

Allometric Models for Predicting Aboveground Biomass in Two Widespread Woody Plants in Hawaii

Allometric models are important for quantifying biomass and carbon storage in terrestrial ecosystems. Generalized allometry exists for tropical trees, but species‐ and site‐specific models are more accurate. We developed species‐specific models to predict aboveground biomass in two of the most ubiquitous natives in Hawaiian forests and shrublands, Metrosideros polymorpha and Dodonaea viscosa. The utility of the M. polymorpha allometry for predicting biomass across a range of sites was explored by comparing size structure (diameter at breast height vs. tree height) of the trees used to develop the models against trees from four M. polymorpha‐dominated forests along a precipitation gradient (1630–2380 mm). We also compared individual tree biomass estimated with the M. polymorpha model against existing generalized equations, and the D. viscosa model with an existing species‐specific model. Our models were highly significant and displayed minimal bias. Metrosideros polymorpha size structures from the three highest precipitation sites fell well within the 95% confidence intervals for the harvested trees, indicating that the models are applicable at these sites. However, size structure in the area with the lowest precipitation differed from those in the higher rainfall sites, emphasizing that care should be taken in applying the models too widely. Existing generalized allometry differed from the M. polymorpha model by up to 88 percent, particularly at the extremes of the data range examined, underestimating biomass in small trees and overestimating in large trees. The existing D. viscosa model underestimated biomass across all sizes by a mean of 43 percent compared to our model. The species‐specific models presented here should enable more accurate estimates of biomass and carbon sequestration in Hawaiian forests and shrublands.     

Analysis of development of a subalpineAbies stand based on the growth processes of individual trees

The progress of growth of a subalpine youngAbies veitchii andA. mariesii forest during 25 years was analyzed on the basis of measurements of the processes of height growth of about 230 trees in a quadrat where the old canopy had been completely destroyed by a typhoon in 1959. The original forest floor sapling population had consisted of trees shorter than 2 m. Saplings grew faster after the breakage of the canopy than before,A. veitchii growing faster thanA. mariesii. During the 25 years of growth, a few well developed trees exceeded 6 m in height, while others remained around only 1 m or less. Some small trees, mostlyA. veitchii died at sites of high density. A bimodality in the distribution of tree height had developed with a trough at about 2.5 m, differentiating the trees into canopy and suppressed populations. Canopy trees grew with wide variation of rates, while most of the suppressed trees showed little recent growth. No difference was found in recent growth rates between the two canopyAbies species. Differences in height growth rates among individual canopy trees were analyzed on the basis of their horizontal crown overlapping. Competition models evaluating the difference in height between trees with overlapping crowns were shown to be effective. The height growth rate of a canopy tree appeared to be controlled by both the closely grown taller trees and the local density of trees including those shorter than the subject tree.     

Acorn production prediction models for five common oak species of the eastern United States

Acorn production varies considerably among oak (Quercus) species, individual trees, years, and locations, which directly affects oak regeneration and populations of wildlife species that depend on acorns for food. Hard mast indices provide a relative ranking and basis for comparison of within- and between-year acorn crop size at a broad scale, but do not provide an estimate of actual acorn yield—the number of acorns that can potentially be produced on a given land area unit based on the species, number, and diameter at breast height (dbh) of oak trees present. We used 10 years of acorn production data from 475 oak trees to develop predictive models of potential average annual hard mast production by five common eastern oak species, based on tree diameter and estimated crown area. We found a weak (R² = 0.08–0.28) relationship between tree dbh and acorn production per unit crown area for most species. The relationship between tree dbh and acorn production per tree was stronger (R² = 0.33–0.57). However, this is because larger-dbh trees generally have larger crowns, not because they have a greater capacity to produce more acorns per unit crown area. Acorn production is highly variable among individual trees. We estimated that dbh of at least 60 dominant or codominant oak trees per species should be randomly sampled to obtain an adequate representation of the range of dbhs (≥12.7 cm dbh) in a given forest area, and achieve precise estimates when using these equations to predict potential acorn production. Our predictive models provide a tool for estimating potential acorn production that land managers and forest planners can apply to oak inventory data to tailor estimates of potential average annual acorn production to different forest management scenarios and multiple spatial scales. © 2011 The Wildlife Society.     

Hollow occurrence and abundance varies with tree characteristics and among species in temperate woodland Eucalyptus

Tree hollows are a critical but diminishing resource for a wide range of fauna around the world. Conservation of these fauna depends on sustainable management of tree species that produce the hollows on which they depend. This study addressed the need for empirical data about intraspecific and interspecific variation in hollow occurrence and abundance in woodland trees in Australia. We measured and performed hollow surveys on 1817 trees of seven species of woodland Eucalyptus in central‐western New South Wales, Australia. Trees were surveyed at 51 one‐hectare sites and about 30% of trees surveyed had multiple stems. Generalized linear mixed models that accounted for nestedness of stems within trees and trees within sites detected a significant amount of variation in hollow occurrence and abundance. Models for individual tree stems of live trees showed hollow probability and abundance increased with diameter at breast height (DBH) and with increasing senescence (form). Stems of Eucalyptus microcarpa Maiden had a higher probability of having hollows than similar DBH stems of Eucalyptus camaldulensis Dehnh., Eucalyptus melliodora A.Cunn. ex Schauer or Eucalyptus populnea ssp. bimbil L.A.S.Johnson & K.D.Hill. Dead stems in live trees were more likely to have hollows than live stems of similar DBH. Each stem in a multi‐stemmed tree had a lower probability of hollow occurrence and lower abundance of hollows than single‐stemmed trees of similar DBH. For stems of dead trees, hollow occurrence and abundance increased with DBH and differed depending on stage of senescence. A comparison of our data with other studies indicates regional variation of hollow abundances within tree species.     

桥山栎林群落结构特征与物种多样性相关关系分析

为了解森林群落结构特征与物种多样性之间的相关关系,以黄土高原桥山林区典型麻栎纯林、麻栎阔叶混交林和麻栎油松混交林为研究对象,调查分析了群落结构特征,计算物种重要值及物种多样性,并进行了冗余分析,结果表明:(1)麻栎油松混交林主要以乔木层胸径、树高、枝下高等最高;麻栎阔叶混交林以灌木层盖度、地径、冠幅、高度等最高;麻栎纯林以草本地径、草本盖度及草本冠幅最高。(2) 3种类型林分乔木层重要值最高的均为麻栎(Quercus acutissima),灌木层为狼牙刺(Sophora viciifolia)、南蛇藤(Celastrus orbiculatus)、胡枝子(Lespedeza bicolor),草本层为苔草(Carex tristachya)。(3)麻栎油松混交林乔、灌层物种多样性较高,麻栎阔叶混交林以草本层物种多样性最高。(4)不同类型麻栎林群落结构特征与物种多样性关系有差异。松栎混交林中,对物种多样性影响最大的为乔木胸径、新稍长及灌木高度;麻栎阔叶混交林对物种多样性影响最大的为灌木层高度及冠幅;麻栎纯林中,对物种多样性影响最大的为乔木胸径。(5)麻栎油松混交林、麻栎阔叶混交林的胸径、树高、物种多样较麻栎纯林高,具有较高木材生产能力和生态防护功能,是未来森林经营培育的方向。     

Allometric equations for integrating remote sensing imagery into forest monitoring programmes

Remote sensing is revolutionizing the way we study forests, and recent technological advances mean we are now able – for the first time – to identify and measure the crown dimensions of individual trees from airborne imagery. Yet to make full use of these data for quantifying forest carbon stocks and dynamics, a new generation of allometric tools which have tree height and crown size at their centre are needed. Here, we compile a global database of 108753 trees for which stem diameter, height and crown diameter have all been measured, including 2395 trees harvested to measure aboveground biomass. Using this database, we develop general allometric models for estimating both the diameter and aboveground biomass of trees from attributes which can be remotely sensed – specifically height and crown diameter. We show that tree height and crown diameter jointly quantify the aboveground biomass of individual trees and find that a single equation predicts stem diameter from these two variables across the world's forests. These new allometric models provide an intuitive way of integrating remote sensing imagery into large‐scale forest monitoring programmes and will be of key importance for parameterizing the next generation of dynamic vegetation models.     

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。     

红松人工林优势木竞争指数影响因子

在温带湿润气候区东段不同立地条件下的红松人工林内设置面积为600 m~2(20 m×30 m)的70块矩形固定样地。在每个样地内,选取5颗最高且长势较好的优势木作为研究的对象木,用Voronoi图确定优势木相应的竞争木,测定每一块样地内优势木与竞争木之间的距离。采用Hegyi单木竞争指数模型,分析优势木在不同样地水平上的种内竞争强度,探讨林分生长因子、地形因子、土壤养分因子对优势木竞争指数的影响,并对这3类因子与优势木竞争指数进行相应的拟合和相关性分析。结果表明：红松人工林优势木竞争强度随着优势木胸径的增大而变小,并且两者之间的关系服从幂函数;红松优势木的竞争指数与其树高、胸径、冠幅呈极显著的相关关系(P<0.01);坡向、坡位、海拔对竞争指数影响极显著(P<0.01);红松人工林优势木竞争指数的大小与土壤氮磷钾含量均呈极显著的相关关系(P<0.01);pH值对优势木竞争指数的影响不显著。当红松人工林优势木平均胸径达到45cm,优势木平均树高和冠幅大于周围竞争木时,其对周围资源的利用程度增大,林木会发生自然稀疏现象,其所受的竞争压力减小。红松喜光性强,对水分的要求高,...     

Biomass functions applicable to Scots pine

This study describes parameterization of biomass functions applicable to Scots pine (Pinus sylvestris, L.) in the conditions of Central Europe. Fifty-two sample trees from seven sites in different regions of the Czech Republic were used for destructive measurements. The observed aboveground biomass (B _AB) and its individual components were examined by different types of non-linear regression models using one to five independent variables including stem diameter (D), tree height (H), tree age (A), crown length (C) and altitude (Z). The best single-equation approximation of B _AB was a three-parameter model using D, H and Z, which was also best suited for bark. Including altitude into classical multiplicative exponential function with three independent variables (DHZ) and four parameters yielded the best model for stem over or under bark. Age was important for assessment of dead branches within DHA model, whereas living branches were best approximated using four variables including C (DHAC model). The most complex model (DHACZ) worked best for needle biomass. The comparison of B _AB assessment by single regression equation and from sum of individual components showed a negligible difference for full-grown trees, whereas the additive assessment yielded considerably higher B _AB for small or young trees. This corresponds to the assessed confidence intervals for individual trees that were larger for smaller trees. The paper also discusses the issue of commonly used linearization of biomass equations and application of linear regression, and provides comparative examples with nonlinear approach used here. The paper presents the parameter sets for the tested equations for B _AB and individual biomass components.     

Allometric Models for Tree Volume and Total Aboveground Biomass in a Tropical Humid Forest in Costa Rica1

Allometric equations for the estimation of tree volume and aboveground biomass in a tropical humid forest were developed based on direct measurements of 19 individuals of seven tree species in Northern Costa Rica. The volume and the biomass of the stems represented about two‐thirds of the total volume and total aboveground biomass, respectively. The average stem volume varied between 4 and 11 Mg/tree and the average total aboveground biomass ranged from 4 to 10 mg/tree. The mean specific gravity of the sampled trees was 0.62 ± 0.06 (g/cm³). The average biomass expansion factor was 1.6 ± 0.2. The best‐fit equations for stem and total volume were of logarithmic form, with diameter at breast height (R²= 0.66 ? 0.81) as an independent variable. The best‐fit equations for total aboveground biomass that were based on combinations of diameter at breast height, and total and commercial height as independent variables had R² values between 0.77 and 0.87. Models recommended for estimating total aboveground biomass are based on diameter at breast height, because the simplicity of these models is advantageous. This variable is easy to measure accurately in the field and is the most common variable recorded in forest inventories. Two widely used models in literature tend to underestimate aboveground biomass in large trees. In contrast, the models developed in this study accurately estimate the total aboveground biomass in these trees.     

Loss of oak dominance in dry-mesic deciduous forests predicted by gap capture methods

Gap capture methods predict future forest canopy species composition from the tallest trees growing in canopy gaps rather than from random samples of shaded understory trees. We used gap capture methods and a simulation approach to forecast canopy composition in three old oak forests (Quercus spp.) on dry-mesic sites in southern Wisconsin, USA. In the simulation, a gap sapling is considered successful if it exceeds a threshold height of 13–17 m (height of maximum crown width of canopy trees) before its crown center can be overtopped by lateral crown growth of mature trees. The composition of both the tallest gap trees and simulated gap captures suggests that 68–90% of the next generation of canopy trees in the stands will consist of non-Quercus species, particularly Ulmus rubra, Carya ovata and Prunus serotina. Quercus species will probably remain as a lesser stand component, with Quercus alba and Quercus rubra predicted to comprise about 19% of successful gap trees across the three stands. Several methods of predicting future canopy composition gave similar results, probably because no gap opportunist species were present in these stands and there was an even distribution of species among height strata in gaps. Gap trees of competing species already average 11–13 m tall, and mean expected time for these trees to reach full canopy height is only 19 years. For these reasons, we suggest that dominance will shift from oaks to other species, even though late successional species (e.g., Acer and Tilia) are not presently common in the understories of these stands.     

Interactive effects of mycorrhization and elevated carbon dioxide on growth of young pedunculate oak (Quercus robur L.) trees

Pedunculate oak (Quercus robur L.) was germinated and grown at ambient CO₂ level and 650 ppmv CO₂ in the presence and absence of the ectomycorrhizal fungus Laccaria laccata for a total of 6 month under nutrient non-limiting conditions. Mycorrhization and elevated atmospheric CO₂ each supported the growth of the trees. Stem height, stem diameter, and dry matter accumulation of pedunculate oak were increased by mycorrhization. Elevated atmospheric CO₂ enhanced stem height, stem diameter, fresh weight and dry weight, as well as lateral root formation of the trees. In combination, mycorrhization and elevated atmospheric CO₂ had a more than additive, positive effect on tree height and biomass accumulation, and further improved lateral root formation of the trees. From these findings it is suggested that the efficiency of the roots in supporting the growth of the shoot is increased in mycorrhized oak trees at elevated atmospheric CO₂.Abbreviations DW dry weight - FW fresh weight - RWC relative water content     

Improved allometric models to estimate the aboveground biomass of tropical trees

Terrestrial carbon stock mapping is important for the successful implementation of climate change mitigation policies. Its accuracy depends on the availability of reliable allometric models to infer oven‐dry aboveground biomass of trees from census data. The degree of uncertainty associated with previously published pantropical aboveground biomass allometries is large. We analyzed a global database of directly harvested trees at 58 sites, spanning a wide range of climatic conditions and vegetation types (4004 trees ≥ 5 cm trunk diameter). When trunk diameter, total tree height, and wood specific gravity were included in the aboveground biomass model as covariates, a single model was found to hold across tropical vegetation types, with no detectable effect of region or environmental factors. The mean percent bias and variance of this model was only slightly higher than that of locally fitted models. Wood specific gravity was an important predictor of aboveground biomass, especially when including a much broader range of vegetation types than previous studies. The generic tree diameter–height relationship depended linearly on a bioclimatic stress variable E, which compounds indices of temperature variability, precipitation variability, and drought intensity. For cases in which total tree height is unavailable for aboveground biomass estimation, a pantropical model incorporating wood density, trunk diameter, and the variable E outperformed previously published models without height. However, to minimize bias, the development of locally derived diameter–height relationships is advised whenever possible. Both new allometric models should contribute to improve the accuracy of biomass assessment protocols in tropical vegetation types, and to advancing our understanding of architectural and evolutionary constraints on woody plant development.     

Double sampling to assess the accuracy of ground‐based surveys of tree hollows in eucalypt woodlands

Ground‐based surveys of tree hollows often give poor estimates of hollow abundance in forests. Woodlands have shorter trees and a more open structure than forests, which may make hollows easier to detect. Therefore, one would expect ground‐based surveys of tree hollows to be more accurate in woodlands than in forests. We compared hollow counts from ground‐based and climbing surveys (double sampling) for four species of Eucalyptus trees in woodlands of central‐western New South Wales, Australia: E. camaldulensis Dehnh, E. melliodora A. Cunn. ex Schauer, E. microcarpa Maiden and E. populnea F. Muell. ssp. bimbil L.A.S. Johnson & K.D. Hill and E. melliodora A. Cunn. ex Schauer. Overall, 83% of hollow‐bearing trees and 93% of trees without hollows were correctly classified by ground‐based surveys. Mean difference in hollow counts of ground‐based surveys to climbed surveys was 1.7 hollows ± 0.2 SE (all species combined) with 91% of ground‐based hollow counts being within five of the actual number of hollows. The error in ground‐based counts of hollows in E. microcarpa was larger than for the other three species. Errors in all species resulted from both overestimation and underestimation of hollow abundance by ground‐based surveys. A larger error was associated with the detection of hollows located in branches compared with hollows located in the main trunk(s). Total number of hollows in the tree (based on climbing surveys), crown area or maximum trunk diameter were significant predictors of ground‐based survey accuracy. Overall, the accuracy associated with ground surveys was relatively high and generally error rates were lower than those published for forests.     

Tree shape plasticity in relation to crown exposure

Trees outside closed forest stands differ in the relation between stem diameter, height and crown volume from trees that grew with neighbours close by. Whether this plasticity in tree shape varies between species in relation to their light requirement is unknown. We purposefully sampled 528 trees ranging 5–100?cm diameter at breast height growing in a range of light conditions. Across ten broad-leaved species observed in Sumatra or Kalimantan, a generic relationship was found between light exposure of the crown and a light-dependent a _l parameter that modifies the height–diameter allometric equation (H?=?a _l D ^b ) from those for closed stands. In our results, vertical stretching is well predicted by light availability. In fully open conditions, trees are on average 31% shorter for the same diameter than under (partial) shade. Most of the stretching response occurs in all species as soon as some degree of lateral shading occurs. The response, however, varies by species (8–44% reduction) in a way apparently unrelated to species’ successional status. Crown volume varied less than stem height in its relationship with stem diameter across all light conditions tested. The scaling of crown volume with stem diameter, however, differed markedly between tree species.     

Primary ecological succession in vascular epiphytes: The species accumulation model

Epiphytes are integral to tropical forests yet little is understood about how succession proceeds in these communities. As trees increase in size they create microhabitats for late‐colonizing species in both small and large branches while maintaining small tree microhabitats for early colonizing species in the small and young branches. Thus, epiphyte succession may follow different models depending on the scale: at the scale of the entire tree, epiphytes may follow a species accumulation model where species are continuously added to the tree as trees increase in size but at the scale of one zone on a branch (e.g., inner crown: 0–2 m from the trunk), they may follow the replacement model of succession seen in terrestrial ecosystems. Assuming tree size as an indicator of tree age, I surveyed 61 Virola koschnyi trees of varying size (2.5–103.3 cm diameter at breast height) in lowland wet tropical forest in Costa Rica to examine how epiphyte communities change through succession. Epiphyte communities in small trees were nested subsets of those in large trees and epiphyte communities became more similar to the largest trees as trees increased in size. Furthermore, epiphyte species in small trees were replaced by mid‐ and late‐successional species in the oldest parts of the tree crown but dispersed toward the younger branches as trees increased in size. Thus, epiphyte succession followed a replacement model in particular zones within treecrowns but a species accumulation model at the scale of the entire tree crown.     

Developmental Patterns of Tree Dimensions in a Neotropical Deciduous Forest1

For 26 tree species in very dry tropical forest in Mexico, the developmental trends of relationships among trunk diameter, tree height, and crown diameter were inferred from a one‐time measurement of dispersed individuals across the size range from saplings to large, mature trees. On hillside sites in this high diversity forest, maximum dimensions were usually <10‐m height, 4‐m crown diameter, and 0.3‐m trunk diameter. The relationship of height to trunk diameter was characterized by an asymptotic, three‐parameter model. Crown diameter was a linear function of trunk diameter. The parameter values for both models varied widely among the species. In general, the dispersion among species of the height–crown diameter relationship increased linearly with trunk diameter (up to 0.2 m). Arborescent cacti were distant from other species at all sizes, although they were well modeled using the same equations. Empirical and theoretical features and limitations of the present and previous models, including mechanical buckling and water‐stress theories, are considered.     

城市林木生物量对硬化地表和种植密度的响应

以北京市典型绿化树种油松、白蜡和元宝枫为实验对象,设置不透水地表、透水地表和对照(自然地表)3种地表类型和低(株行距为2.0 m×2.0 m)、中(1.0 m×1.0 m)、高(0.5 m×0.5 m)3个种植密度,经过6年的生长,对树木的生长和生物量进行了测定。结果表明：相比于对照,不透水地表下油松、白蜡和元宝枫的树高生长受到抑制,白蜡和元宝枫的单株生物量分别降低2.1%—27.1%和33.6%—52.3%,根冠比分别增加3.4%—25.8%和15.7%—23.4%。相比于不透水地表,透水地表下白蜡和元宝枫的树高显著增加,白蜡的单株生物量增加5.3%—45.5%,根冠比下降11.4%—18.7%。随着密度的增加,3种树木的基径和单株生物量显著降低,但中低密度下的单位面积生物量无显著性差异。此外,硬化地表与种植密度对树木的基径、树高、单株生物量和根冠比均无显著的交互作用。因此,在城市绿化中,采用透水地表来替代不透水地表,有利于改善树木生境进而促进树木生长。白蜡相比元宝枫更能适应硬化地表的不利影响,是更好的城市绿化树种的选择。同时,合理的种植密度是保证城市树木生长的重要因素。     

基于树冠重叠面积的天然混交林林木竞争指数

构建基于树冠重叠面积和林木混交关系的竞争指数,探究天然混交林林分及主要树种竞争的表达方法,并以甘肃省小陇山林区锐齿槲栎天然混交林为研究对象,采用胸径、树高、冠幅、距离等信息的2期调查数据,对新构建的基于树冠重叠面积的天然混交林林木竞争(CIM)指数进行验证,并选取Spearman系数,对CIM竞争指数和传统竞争指数进行相关性分析。结果表明,采用树冠投影重叠和考虑树高关系确定竞争木的方法能有效避免竞争木多选或漏选; CIM1、CIM2、CIM3能够表达出混交林竞争压力变化,表现出竞争压力越大林木蓄积生长量越小的趋势,将树种混交因子引入竞争指数能够提高蓄积生长量与竞争指数的相关性,更加客观的描述林分中竞争状况。竞争指数与蓄积生长量相关性由大到小排序为CIM2>CIM3>CIM1>Bella竞争指数(CIO)>简单竞争指数(CI)>CIO2>CIO1,表明竞争指数 CIM2对混交林竞争表达更具参考意义。林分中主要树种锐齿槲栎由于相邻木中同树种相邻木增加,导致竞争压力增大。天然混交林中树种组成复杂多样,林木分布不均匀,在竞争指数中引入树种混交因子能够较为真实的反映林木竞争状况。