DIGITALNA ARHIVA ŠUMARSKOG LISTA
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ŠUMARSKI LIST 1-2/2012 str. 18 <-- 18 --> PDF |
Ž. Škvorc, K. Sever, J. Franjić, D. Krstonošić, M. Poljak: INTENZITET FOTOSINTEZE I VEGETATIVNI ... Šumarski list br. 1–2, CXXXVI (2012), 7-17 ves in the crown of a tree temporarily lose their green color and turn yellow, which is indicative of plant’s lack of nitrogen nutrition, i.e. the nitrogen deficiency in the soil. The role of nitrogen as a plant nutriment is connected with numerous physiological processes responsible for successful growth and development of plants. For example, nitrogen is an essential element responsible for an uninterrupted continuation of photosynthetic process and vegetative plant growth, primarily because of its role in the synthesis of chlorophyll and certain proteins, such as ribulose-1,5-bisphosphate carboxylase oxygenase (Rubisco), which is responsible for CO2assimilation. In the previous studies of forest trees, significant differences were determined in the intensity of photosynthesis and vegetative development regarding the diverse conditions in the habitats. These variations are usually due to the lengths of summer droughts and high temperatures, the intensity of illumination, and the differences between dry and wet years. The aim of this study was to, (1) determine the effect of various chemical characteristics of the soil on the intensity of photosynthesis and the vegetative growth of pedunculate oak, (2) establish a connection between content index of the total amount of chlorophyll in the leaf, and the intensity of photosynthesis and the vegetative growth of pedunculate oak. The study was conducted during the vegetative period in 2010, on 4-yearold plants, planted with 2 – 2,5 meters of space between plants. Based on visual differences in the leaf color, two plots have been set aside – the chlorotic and the control plots (without chlorosis). Each field contained 8 plants, i.e. 16 in total. The average height of the plants under study before the start amounted to 1.96 ± 0.44 meters, and the diameter of the trunk 2.5 centimeters, measured 30 centimeters above ground. In order to determine the differences in the soil’s chemical characteristics between the two studied plots, the samples were taken on the depth of 0–30 centimeters. The soil reaction was determined with a potentiometer in the suspension of soil and water, i.e. soil and nKCl. Humus was determined by the Thorin method, and the total nitrogen level by the Kendahl method. The content of physiologically active phosphorus and potassium was determined by the Al-method. The study determined height and diameter increment for the plants studied, and also height and diameter increment for primary branches of each plant. The number of spring and summer shoots with its attending leaves was also determined. Based on the number and surface area of leaves, as well as the projection of crown surface on the ground, index of leaf surface was calculated for each tree. The measurements of photosynthesis intensity and the index of total chlorophyll content were performed early in September. The photosynthesis intensity was measured with the help of the infrared gas analizer portable device LCpro + (ADC BioScientific). While taking photosynthesis intensity measurements, each leaf was subjected to illumination intensity of 1500 µmol m-2 s-1, CO2concentration of 380 ± 10 µmol mol-1and the air temperature of 25 ± 2 °C. The chlorophyll content index was determined by using chlorophyll content meter CCM-200. By using a portable chamber for measuring water potential, the measurement of water potential was taken in the leaves (.) of plants under study. The chemical characteristics of the soil in the test plots were shown in Table 1. There was an extremely acidic reaction in the chlorotic plot, and acidic in the control plot. The chlorotic plot was marked by an extremely low nitrogen supply, while the control plot had a medium to good nitrogen supply. The content of physiologically active phosphorus in the chlorotic plot was ex |