Stand characteristics,understorey associates and environmental correlates ofEucalyptus tetrodonta F. Muell. forests on Gunn Point,northern Australia

An ordination study of 20Eucalyptus tetrodonta forest stands growing on deep earths in monsoonal Australia revealed two major gradients in understorey vegetation type. The first axis reflected both floristic and structural understorey variation, where litter and shrub cover were inversely related to grass cover. This axis is thought to reflect a complex fire-vegetation type interaction, where vegetation is primarily determined by the saturation of the soil profile in the wet season, as measured by the colour of the iron rich soils. On the second axis of the ordination, floristic composition but not vegetation structure, and stand height were found to vary with the intercorrelated measures of soil gravel and moisture supply.E. tetrodonta is able to regenerate in the absence of fire, but firing appears to stimulate regeneration. All stands contained some advance growth, which occurs in distinct clumps, probably reflecting these plants clonal origin. Sapling presence in the stands is variable and the recruitment of advance growth into this size class appears to be related to over-wood competition. The size class distribution of trees was found to be similar amongst the stands, therefore stand structure appeared to be independent of understorey type. In comparison to general models of temperate eucalypt regeneration processes the tropical eucalypts have evolved different regeneration strategies, possibly in response to the severe annual drought.Nomenclature: Chippendale (1971), unless otherwise indicated. Structural classification: Specht (1970).I acknowledge the help of Mr. Clyde Dunlop who identified plant specimens and provided stimulating discussion, and Dr. Peter Minchin for permission to use the computer package ECOPACK to prepare and handle the floristic data, and his invaluable assistance with the ordination analysis. Mr. Lee Belbin and CSIRO Division of Water and Land Resources kindly gave their permission to use the Numerical Taxonomy Package (NTP).     

Crop production and management under saline conditions

Summary This review evaluates management practices that may minimize yield reduction under saline conditions according to three strategies: (I) control of root-zone salinity; (II) reduced damage to the crop; (III) reduced damage to individual plants. Plant response to salinity is described by an unchanged yield up to a threshold soil salinity (a), then a linear reduction in relative yield (b), to a maximum soil salinity that corresponds to zero yield (Y_o). Strategies I and II do not take into consideration any change in the parameters of the response curve, while strategy III is aimed at modifying them.Control of root zone salinity is obtained by irrigation and leaching. From the review of existing data it is concluded that the effective soil salinity parameter should be taken as the mean electrical conductivity of the saturated paste extract or of the soil solution over time and space. Several irrigation and leaching practices are discussed. It is shown that intermittent leaching is more advantageous than leaching at each irrigation. Specific cultivation and irrigation practices that result in soil salinity reduction adjacent to young seedlings and the use of water of low salinity at specifically sensitive growth stages may be highly beneficial. Recent data do not show that reduced irrigation intervals improve crop response more under saline than under nonsaline irrigation. Alternate use of water of different salt concentrations results in mixing in the soil and the crop responds to the mean water salinity.Reduced damage at the fiel level when soil or irrigation water salinity is too high to maintain full yield of single plants requires a larger crop stand. For row crops reduced inter-row spacing is more effective than reduced intra-row spacing.Reduced damage at the plant level while the salinity tolerance of the plants remains constant shows up in the response curve parameters as larger threshold and slope and constant salinity at zero yield. This is the effect of a reduced atmospheric water demand that results in reduced stress in the plant under given salinity. Management can also change the salt tolerance of the crop. This will show up as higher salinity at zero yield, as well as changes in threshold and slope. Such changes in the response curve were found at different growth stages, under different atmospheric CO₂, under different fertilization, and when sprinkler irrigation was compared with drip irrigation.Contribution from the Agricultural Research Organization, The Volcani Center, Bet Dagan, Israel. No. 1111-E 1984 series.     

林分随机生长模型与Richard模型

本文从一般的假设出发,很自然导出连续状态空间的树木直径分布生长方程,证明此方程解的存在性,并给出一个例子说明Richards方程是直径分布生长方程的一个特解的二阶矩．     

山杨林林分密度效应动态模拟

 本文用林窗模型研究了小兴安岭南坡山杨林林分密度动态过程,在给定林分初始条件后,模拟了林分密度、断面积、生物量、叶面积指数和生产力150年的变化。用林分密度效应的3/2法则和产量恒定法则检验模拟林分,结果表明模拟林分密度发展与理论预测相符合。通过本文的研究既检验了林窗动态模型又印证了林分密度效应理论。     

兴安落叶松原始林年龄结构动态的研究

对受不同程度干扰的兴安落叶松原始林年龄结构的研究表明,一代林年龄结构动态的特点是初期种群密度增大,年龄变幅加大,后期因自然稀疏而年龄变幅减小。多代林是不同世代的一代林的斑块镶嵌,上层老年世代年龄变差小,中层的中年或成年世代变差大,下层幼年世代变差亦较小。白桦与落叶松在良好立地上混生时,初期因白桦定居早,其平均年龄比落叶松大5—15年,50—70年后,落叶松的平均年龄因部分白桦死去而变得较大。     

Analysis of stand density effects on canopy structure: a conceptual approach

Summary A few assumptions were used to generate a series of specific, quantitative predictions for the relationships between stand density and various dimensional measures of canopy structure. The predictions, each indicating an increase in mean crown size as density decreased, appeared to be reasonable and intuitive. Predictions were compared to data for two conifer species with different crown forms, Pinus contorta var. latifolia and Abies lasiocarpa. Results of these comparisons were mixed — the linear, directly measured dimensions were consistent with predicted relationships, but dimensions calculated from the linear measures were not. Re-examination of the original assumptions indicated that the model should account for crown shyness (engagement/disengagement) to adequately reflect the influence of stand density on canopy structure. The results also indicated a strong association between stand height and measures of mean crown size. Mean crown size of lodgepole pine was altered much more by density than was mean crown size of subalpine fir, due primarily to the different relative shade tolerances of the two species. Some of the observed differences between species may also reflect the range of densities examined and uneven spacing in the unmanaged natural stands.     

The effect of two growth forms of Norway spruce on stand development and radiation interception: a model analysis

Summary Development of tree and canopy structure, and interception of photosynthetically active radiation (PAR) were studied in two model stands of Norway spruce consisting of trees with rapid versus slow site capture. The tree models were derived using Burger's (1953) sample tree material, from which two subpopulations of dominant trees were selected using the rate of horizontal site capture of the tree crowns as the criterion of division. The development of stand structure and interception of PAR were simulated in the two model canopies. The simulation period covered the period from tree age 15–80 years. The average development of the trees in the two subpopulations proved to be very different. The rapidly expanding trees were characterized by low mean within-crown needle area density and a long crown. The slowly expanding trees were smaller but had a higher mean within-crown needle area density. Up to approximately 40 years of age the stand of rapidly expanding trees contained more leaf area and intercepted more radiation than the stand of slowly expanding trees, when canopy cover was held constant. After 40 years of age this relationship was reversed due to the subsequent decline of leaf area in the stand of rapidly expanding trees and the increase in leaf area in the stand of slowly expanding trees. The biological relevancy and silvicultural implications of the simulated patterns of tree and stand development are discussed.     

Amelanchier alnifolia vegetation in eastern Idaho,USA and its environmental relationships

Fifteen shrub stands of Amelanchier alnifolia vegetation were studied using Braun-Blanquet procedures, tabulated, and ordered by Twinspan, Decorana, and field experience into 5 groups of stands. The stands occurred on the lower slopes of the southwestern Teton and southeastern Big Hole mountains of eastern Idaho and in-and outside a U.S. Forest Service exclosure above the Hoback River in adjacent Wyoming. The ecology of this Amelanchier vegetation as a whole and of the 5 groups of stands is discussed using Jenny's factors of soil formation (1941, 1958, 1980) as a framework. Plant indicator values (Ellenberg 1979, 1988) which rank species on their occurrences in relation to light, temperature, continentality of climate, water availability, soil reaction (pH), and soil nitrogen supply, were independently assigned to the 121 species of vascular plants encountered in the described stands.     

Natural regeneration of forest related to the spatial structure of trees: A study of two forest communities in Western Carpathians,southern Poland

The existence of a relationship between the spatial pattern of trees and the distribution of young individuals beneath the canopy has been tested in the beech (Fagus sylvatica) and spruce (Picea abies) — fir (Abies alba) forests in the mountainous region, using two different methods. The first method was the analysis of spatial pattern of individuals, the second one was based on calculating sums of influences of all trees occurring within analysed plot on a given point on the forest floor. Results of spatial pattern analyses were surprisingly consistent: almost all mature trees and seedlings didplayed a random pattern of spatial arrangement. However, there is a clear, although statistically insignificant tendency towards uniformity of spatial pattern with increasing sizes of analysed trees. Results of comparing sums of influences on regularly distributed points with sums of influences on seedlings or saplings revealed no tendency in forest regeneration to concentrate in places, where the sums were smaller than the average for a plot. This, coupled with the dominance of random spatial pattern of trees, suggests, that viewed on a small spatial scale, influence of competition among forest trees on their spatial arrangement is obscured by other factors, which are not closely related to the distribution of individuals.     

Variation of soil carbon pools in Pinus sylvestris plantations of different ages in north China

Plantations play an important role in absorbing atmospheric CO₂ and plantation soil can serve as an important carbon (C) sink. However, the stocks and dynamics of soil C in differently aged plantation forests in north China remain uncertain. In this study, we measured soil inorganic carbon (SIC), soil organic carbon (SOC) and total nitrogen content (STN), the light (LF) and heavy fractions (HF) of soil organic matter (SOM) to a depth of 1 m in 3 different ages (10-, 30-, 40-year-old) of Pinus sylvestris var. mongolica (Mongolia pine) plantations in 2011 and 2012. Soil pH, texture and moisture were also measured to explore the causes of SOC dynamics for different stand ages. Our results showed that no significant difference in SIC content was observed at different soil depths. As forest age increases, SIC content as well as the C and N content in SOM, LF and HF initially rose and then decreased, while the LF in SOC initially decreased and then increased. Although the C:N ratio of SOC and HF did not significantly change, the C:N ratio of LF increased with depth. SOC dynamics at different stand ages were significantly correlated with soil moisture and clay content. Soil pH and moisture explained 58.63% of the overall variation of SOC at different depths. Moreover, the SOC increased during the early stage of afforestation, mostly because of the increase in recalcitrant C; however, the decrease of SOC with increasing stand age was also mainly affected by C loss in the recalcitrant C pool.