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We used the needle trace method to investigate changes in the state of a Scots pine (Pinus sylvestris L.) stand in a bog (Voorepera) in the north-eastern part of Estonia, the most polluted area of the country. Additionally, we chose six sampling sites in other parts of Northeast Estonia (polluted area) and eight sites in southern Estonia (unpolluted area) to compare the state of pine stands in different bogs. During the period of 1964–1997, the radial growth had increased from 0.27 to 2.16 mm yr–1 and the annual shoot length from 0.10 to 0.28 m in Voorepera. Mean values of the period (1.13 mm yr–1 and 0.26 m, respectively) were two and four times higher in Voorepera than the average of the other bogs (0.5 mm yr–1 and 0.06 m, respectively). Maximum needle age fluctuated between three and five growing seasons in Voorepera, the mean (four growing seasons) was similar to that of other bogs (four growing seasons). Except radial growth, which was 0.6 mm yr–1 in the polluted area and 0.4 mm yr–1 in the unpolluted area, other indices of trees' health (shoot growth, needle age, nitrogen concentration in needles) and substrate conditions (water pH and N concentration) did not show clear differences between polluted and unpolluted areas. We conclude that air pollution from oil shale industry (thermal power plant and chemical factories) enhances the growth of pines in bogs, which can induce drastic changes in these ecosystems. However, the effect is currently obvious only in the vicinity of pollution sources.  相似文献   
2.
Pensa M  Jalkanen R 《Tree physiology》2005,25(10):1265-1271
Latitudinal variation in needle longevity of conifers in response to climatic variability is a well-known phenomenon, but its significance has only rarely been studied. Scots pine (Pinus sylvestris L.) stands were investigated in four locations in Lapland (northern Finland and northern Sweden, 67-68 degrees N) and in four locations in Estonia (59 degrees N) to test the hypothesis that plasticity in needle longevity results in similar needle biomass per foliated shoot length across latitudes. The needle-trace method (NTM) revealed the dynamics of needle fascicles attached to stem shoots. Long-term mean needle age was 2 years greater in Lapland than in Estonia. In both regions, mean needle age was strongly and negatively related to yearly needle-fascicle production rate relative to the number of needles on the same shoot axis. Although significantly fewer needle-fascicles were produced annually in trees in Lapland than in Estonia, the overall number of fascicles attached to the stem shoots, needle-fascicle density and individual needle dry mass did not differ between regions. Consequently, needle biomass per foliated shoot length was similar in trees in both regions. Thus, our results support the theory that plasticity in needle longevity helps Scots pine to compensate for reduced needle production so that the same foliar biomass per shoot is retained under a wide range of growth conditions.  相似文献   
3.
Atmospheric air pollution levels and long-term effects on the environment caused by simultaneous presence of SO2 and oil shale alkaline fly ash during the last five decades (since 1950) were investigated. The annual critical value of SO2 for forest (20 µg m?3) was surpassed in 1% (~35 km2) of the study area where the load was 30–40 µg m?3. No effect of long-term SO2 concentrations of up to 10–11 µg m?3 (0.5-h max up to 270 µg m?3) and simultaneous fly ash loads of up to 95 µg m?3 (1000 µg m?3) on the growth and needle longevity of Pinus sylvestris was established. The yearly deposition (average load up to 20–100 kg S ha?1) was alkaline rather than acidic due to an elevated base cation deposition in 1960–1989. Since 1990, the proportion of SO2 in the balance of components increased: about 70–85% of the total area was affected while the ratio of annual average concentrations of SO2 to fly ash was over 1. The limit values of fly ash for Sphagnum mosses and conifers in the presence of SO2 are recommended.  相似文献   
4.
Scope and Goal  Humic substances (HSs) are the product of microbial degradation, chemical polymerisation and oxidation of organic matter. HSs can be divided into different fractions: humic acid (HA), hymatomelanic acid (HMA), fulvic acid (FA) and humin. HSs play a fundamental role in accumulation and exchange processes of chemical compounds (metals and organic pollutants) in the environment. HSs can form soluble complexes that migrate long distances or precipitate, carrying bound cations with them. The migration/precipitation abilities depend on the metal ion, the ion charge, the degree of ionisation of the organic molecule, the ionic strength of the media, and the location of the metal ion. Objective  Estonia is rich in the Baltic Sea and lake sediments. Historically, mud has been used in human treatment as a curative mud. High-molecular HSs are an important part of curative mud and they have a strong effect on its properties. The curative mud which is used in human therapy may not be polluted with different organic and inorganic contaminants. The aim of this work is to characterise and compare HSs isolated from the Baltic Sea mud (Haapsalu Bay) and from the sediments of Lake Ermistu (Estonia). Results and Conclusions  We determined the yield of basic extraction of different HSs components from mud in the course of separation. We found that acid pre-treatment of mud increased the amount of extracted HSs more in the sea mud than in the lake mud. These results show that HSs are bound to the inorganic/organic structure of mud and are released during prolonged treatment with an acid. We performed elemental analysis of the different fractions of HS extracts. HMA fractions had the highest carbon content and the lowest nitrogen content. HMA contains more polysaccharides than amino acid residues. These subunits may cause a better solubility of HMA in water as compared to HA. Acid pre-treatment of the natural sea and the lake mud diminished the content of carbon in most of the HS fractions. The content of nitrogen in the sea and in lake FA diminished by about two times. We determined the metal content in the mud and its HS fractions. We found that the concentration of heavy metals Pb and Cr is lower than <0.08 mg/kg. As expected, the total metal concentration is considerably lower in the lake than in the sea mud. Acid pre-treatment of mud shows that the sea HA forms more stable Fe and Mg complexes, while the sea HMA contains more stable Zn and Cu complexes. The lake HSs result in more stable Mg complexes with HA and HMA fractions. Sea FA binds Cu and Mg better, but lake FA is more effective in binding Zn. To compare the amount of metals extracted from HA, HMA, FA (with that, remains in HS fractions), the metal concentration in the alkaline full extract of the sea mud was determined. Alkaline treatment removed 0.8% Mg, 7.9% Cu, 5.2% Zn and 3.8% Fe together with HSs from the sea mud, the rest remained in humin and in the mineral part of the mud. The following work-up was additionally carried out for most of the metals. So, we found that there was only 1.7% of Fe, 2.1 % of Mg, 23.2% of Zn and 45.2% of Cu left in HA, HMA and the FA fraction (as a sum) from the total amount of those metals in HSs. This means that Cu is the metal most strongly bound to HSs. On the bases of HS separation data we found that the order of stability of the metal-humate complexes is Cu>Zn>Mg>Fe. The ultraviolet spectra of HA, HMA and FA revealed that HMA had the biggest molar absorption and calculated aromaticity. Recommendations and Outlook. The characteristics of HSs, isolated from the Baltic Sea and Lake Ermistu mud reveal the difference of HSs from the sea and the lake mud. Also, different properties of HS fractions are observed. Metals are concentrated variously in different HS fractions. In all cases the content of Pb and Cr was low, meaning that the mud preparations are nontoxic in respect to these metals. The order of stability of metal-humate complexes is Cu>Zn>Mg>Fe. The order of affinity of metals to HS fractions obtained have to be extended to other metals of environmental interest. The ability of HSs to bind metals may make them a candidate for natural, environmentally safe substances to concentrate hazardous metals and to remove them from natural water reservoirs.  相似文献   
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