Current issue: 57(2)
Under compilation: 57(3)
A metabolic model of height growth and site index is derived from a parametrization of the annual carbon balance of a tree. The parametrization is based on pipe-model theory. Four principal variants of the height-growth model correspond to four combinations of assumptions regarding carbon allocation: (a) the apical shoot is autonomous or (b) it is not; and (A) the specific rate of elongation of a shoot equals that of a woody root or (B) it does not. The bB model is the most general as it includes the aA, bA, and aB models as special cases. If the physiological parameters are constant, then the aA model reduces to the form of the Mitscherlich model and the bA model to the form of a Bertalanffy model. Responses of height growth to year-to-year variation in atmospheric conditions are rendered through adjustments of a subset of the model's parameters, namely, the specific rate of production of carbon substrate and three specific rates of maintenance respiration. As an example, the effect of the increasing atmospheric concentration of CO2 on the time-course of tree height of loblolly pine (Pinus taeda) is projected over 50-year span from 1986. Site index is predicted to increase and, more importantly, the shape of the site-index curve is predicted to change.
The present study is the first attempt to carry out an inventory of greenhouse gas (GHG) fluxes in the forests of Estonia. The emission and uptake of CO2 as a result of forest management, forest conversion and abandonment of cultivated lands in Estonia was estimated. The removal of GHG by Estonian forests in 1990 exceeded the release about 3.3 times. Changes in the species composition and productivity of forest sites under various simulated climate change scenarios have been predicted by using the Forest Gap Model for the central and coastal areas of Estonia. The computational examples showed that the changes in forest community would be essential.
Willows (Salix phylicifolia) were grown for four months in organic rich soil at four nutrient levels (fertilization with a micronutrient-macronutrient mixture of 0, 100, 500 and 1,000 kg ha-1 per month) and four CO2 concentrations (300, 500, 700 and 1,000 ppm). Nitrogen and phosphorus concentration of the willows were reduced at CO2 enhancement, the decrease being larger in the leave and roots than in the stems. Nitrogen content of the willows plus extractable nitrate-N in the soil coincided well with the doses of nitrogen supplied, but the corresponding sum of phosphorus in the plants and soil were smaller. The total nitrogen content of willows grown in unfertilized soil was nearly two times higher than the sum of the extractable nitrate-N in soil and N content of the cutting at the beginning of the experiment. The contents of nitrogen and phosphorus of the unfertilized willows were independent of CO2 concentration, suggesting that CO2 concentration did not affect through increased mineralization the availability of those nutrients to the willows.
A total of 1,800 3-year old seedlings of Norway spruce (Picea abies (L.) H. Karst.) from two Norwegian and one German provenance were treated with two different nitrogen levels during the 1992 growth season. The plants were kept during the following winter at two different temperature levels. In the spring of 1993, the nutrient application was resumed, and the plants were divided between three different treatments, 350 and 650 p.p.m. in open top chamber and a control plot outside the chambers. This treatment was repeated also during the following 1994 growth season.
The growth and primary production were studied by photosynthesis experiments and by non-destructive growth measurements. The result indicate that raised winter temperature may lead to increased needle loss and reduced growth the following season, particularly in northern provenances. Carbon dioxide significantly influenced growth in addition to nutrient level and winter temperature. High CO2 also seemed to cause increased photosynthesis at early season, and earlier budbreak and growth cessation than in control plants.
The Värriö environmental measurement station has been designed and constructed during 1991 and 1992. The measurement system consists of measurement units for gases (sulphur dioxide, ozone, carbon dioxide), particles, photosynthesis and irradiation. A meteorological station is also included. The preliminary measurement period was started on August, 1991. During the first year (1991–1992) some parts of the system were redeveloped and rebuilt. Full, continuous measurement started in August 1992. The system has been working quite reliably, with good accuracy. The preliminary results show that pollution episodes are observed when the wind direction is from Monchegorsk or Nikel, the main emission sources in Kola Peninsula.
In the literature review the current status of information on the genetic variation of CO2 exchange and some reviews and investigations on this subject are listed. Photorespiration is separately discussed and unpublished data of an electron microscope study of poplar leaf microbodies are presented.
Considerable genetic inter- and intraspecific variation is found in several characteristics that affect CO2 exchange in trees. Photosynthesis in young trees does not correlate well with growth through the whole rotation cycle. A special interest has been shown to marginal environmental conditions (e.g. water deficit, low temperature, and low light intensity), as opposed to optimal conditions often employed in laboratory studies of CO2 exchange in trees.
In an unpublished poplar studies by the author et.al. a preliminary experiment with poplar clones showed variation in the CO2 competition point. This variation was negatively correlated with the photosynthesis efficiency of these clones.
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Growth-promoting effects of enhanced caron dioxide levels upon forest tree seedlings grown in plastic houses was studied in 1964 and 1965 in the Forest Breeding Foundation in Haapastensyrjä near Loppi in Southern Finland. In both years more vigorous height and weight growth, and development of root system was achieved when the CO2 concentration was increased to 0.2% than in the normal conditions (CO2 0.03%). The CO2 concentration was increased by burning propane in the plastic houses. Burning continued for four hours per day either at 8–10 and 14–16 a clock or 6–10 a clock. Growth was not affected by the time of the treatment, and it was equally high in 0.1% and 0.2% concentrations.
Treatment of the seedlings with 100–200 ppm gibberellic acid (GA) increased the height growth of healthy, well-rooted seedlings. Treatment with a concentrated (600 ppm) dosage, as well as treatment with a combination of GA and 1-naphtyl acetic acid (NAA) caused serious defects in grafts of Scots pine (Pinus sylvestris L.). GA treatments did not induce flower formation in pine. Red light during the night seemed to enhance growth of grafts of silver birch (Betula pendula Roth) and Norway spruce (Picea abies (L.) H. Karst.).
The PDF includes a summary in Finnish.
Plants assimilate carbon dioxide from the air. Respiration of plants also produce carbon dioxide. Because the carbon dioxide level of the air is only 0.3%, only little carbon dioxide can diffuse in plants. Thus, the carbon dioxide assimilated by the plants is formed mostly in the earth when organic substances are degraded. The article describes a method to measure carbon dioxide level in the air.
The aim of this study was to investigate the ecophysiological and morphological characteristics of two salt-tolerant tree species, Eucalyptus camaldulensis Dehn. and Combretum quadrangulare Kurz. A greenhouse experiment with different levels of NaCl salinity (0, 0.5, 1.0, 1.5, and 2.0%) was set up and the results were compared with those of a field study on non-saline and saline soils. The determination of optimum gas exchange and the development and evaluation of photosynthetic models with and without water deficit were also included in this study.
Morphological characteristics under saline conditions showed that shoot height and diameter growth, shoot internode length, root length/biomass, leaf width and length, leaf area, number and biomass, and shoot/root and leaf/root ratios decreased with salinity, while leaf thickness increased with salinity. More growth was allocated to the roots than to the leaf canopy. Ecophysiological studies in laboratory showed that photosynthesis, stomatal conductance and water potential decreased with salinity, while the CO2 compensation point increased with salinity. Transpiration, dark respiration and photorespiration increased at low salinity but decreased at high salinity levels. In the field study, however, there were no significant differences in stomatal conductance and opening between saline and non-saline soils. Model predictions supported the results of the field measurements. Adaptation to salinity was reflected in an acclimatization of tree structure in the field study. There were both functioning and structural changes of seedlings in the greenhouse experiment
In terms of ecophysiological and morphological characteristics, E. Camaldulensis showed better salt tolerance than C. Quadragulare both in the greenhouse experiment and field study
The PDF includes a summary in Finnish.
Genetic variation in the physiological characteristics and biomass accumulation of Acacia mangium Willd. was studied in both field and laboratory conditions. Variation in the growth characteristics, foliar nutrient concentration, phyllode anatomy and stomatal frequency was analysed in 16 different origins under field conditions in Central Thailand. Family variation and heritability of growth and flowering frequency were calculated using 20 open-pollinated families at the age of 28 months. The effect of environmental factors on diameter growth in different provenances is also discussed.
Under laboratory conditions, such physiological characteristics as transpiration rate, leaf conductance and leaf water potential were measured at varying soil moisture conditions. The responses of photosynthesis, photorespiration and dark respiration as well as the CO2 compensation point to temperature and irradiance were also investigated. All physiological characteristics indicated differences among provenances. An attempt was made to relate the results obtained in the laboratory to the growth performance in the field. Recommendations on provenance selection for the planting of A. mangium in Thailand are also given.
The PDF includes a summary in Finnish.