Determination of microbial activity and nitrogen and carbon forms in peat soils in Estonia M. Noormets1,2, T. Köster1, T. Tõnutare1, K. Kauer1, R. Kõlli1 & K. Karp2 1 Department of Soil Science and Agrochemistry, Estonian Agricultural University, Estonia 2 Department of Horticulture, Estonian Agricultural University, Estonia Abstract For plants in order to grow in different types of peat soils the microbial activity and the release of nutrients is important. Therefore, it is important to perform the monitoring of exhausted peat fields and peat lands in their natural state in order to understand better their pedoecologial conditions. In the present study we examined different nitrogen and carbon forms, and microbial activity, as well as several agrochemical parameters in the different peat soils. Five study areas are located in the county of Tartu (58° 22’ N, 26° 43’ E) in the southern part of Estonia. One of the study areas is located in the county of Harjumaa (59° 6' N, 25° 22' E) in the north-western part of Estonia. The soil of the experimental fields belongs to the soil subgroups of Fibri–Dystric Histosol according to the WRB soil classification (1, 2, 3, 4 study area), with a soil acidity pHKCl 2.7-4.6. The rest of the soils were Endorupti-Dystric Histosol (5) with pHKCl 2.5-2.7 and Eutri-Fluvic Histosol (6) with pHKCl 6.5-7.2. The preliminary results of this study suggest that the differences in the studied parameters are representative. The study will also provide information about the possibility to use some peat soils for recultivation. After comparison of the different ecosystems, the lowest microbial biomass was found in the flood-plain Eutri-Fluvic Histosol with the lowest content of organic carbon (27.4 %). The content of available plant nutrients was medium to high while for phosphorus it was very low or low for all the investigated peat soils starting from 6.8 mg kg-1 at Fibri-Dystric Histosol in Sangla without plant cover and reaching 36.7 Pavb, mg kg-1 in Sapi-Lulli covered by V. angustifolium. Keywords: respiration rate, ash content, total biomass, mineralized N, biomass C, biomass N, nutrients, peat soils. Geo-Environment, J. F. Martin-Duque, C. A. Brebbia, A. E. Godfrey & J. R. Diaz de Teran (Editors) © 2004 WIT Press, www.witpress.com, ISBN 1-85312-723-X 60 Geo-Environment 1 Introduction The total territory of Estonia is 45 227 km², of which 23% is covered by mires [22]. It is the largest area of mires in Northern Europe. The total area of mires is 1, 009, 101 ha while in the focus of processors there are 477, 000 ha because of the peat deposition [28]. The total area of exhausted peat fields will be doubled in the near future as a result of intensive peat production and there will be more abandoned areas added to the already existing 22,000 – 24,000 ha. During the recent decades, with the increasing threat of global climatic change, there has been more discussion about the importance of peat soils in the global C turnover. The issue of sinks and sources of CO2 and other gases, responsible for the climatic changes has been in the centre of attention of many research interests [4, 9]. As the peat soils are sensitive to agricultural activities, especially soil tillage, then the choice of the right species is important. After peat excavation the natural plant succession is very slow to occur, unless the seed bank is presented in topsoil [18, 21]. The agricultural use of peat soils includes draining that will destroy the natural water system and disturb the normal water balance in that area and in the neighbouring areas as well. In some cases unbalanced fertilization is leading to eutrophication. The ombotrophic bogs are known by nutrient poor environment. The capacity of these soils to ensure plants with nutrients depends on atmospheric inputs. The opencast peat fields are very poor in essential nutrients (N, P, and K) present in the accessible forms for plants where the additional inputs of balanced fertilization is important for plants growth [20]. Moreover, in the opencast peat fields where the natural bog water system and the plant cover is destroyed the mineralization and surface deflation is very fast if to compare with peat formation. Rapid mineralization of organic matter in drained and managed peatlands lowers the soil surface at an average rate of 3 cm per year, as calculated for peatlands in the temperate zone [10]. The aim of the current study is to evaluate the content and the characteristics of different soil organic matter from different soils on investigation areas and to establish how they differed from each other by plant cover, exploitation and the soil type. 2 Materials and methods The five study areas (1, 3, 4, 5, and 6) are located in the county of Tartu (58° 22’ N, 26° 43’ E), in the southern part of Estonia. The study area 2 is located in the Harju county (59° 6' N, 25° 22' E) in the north-western part of Estonia. The soil of the experimental fields belongs according to the WRB soil classification, to the soils subgroups of Fibri–Dystric Histosols (1, 2, 3, and 4 study area). The rest of soils were Endorupti-Ombric Histosols (5) and Eutri-Fluvic Histosols (6). The plant associations of the investigated areas are determined according to the classification system developed by J. Paal [23]. Investigation area Sangla is used currently for peat excavation, therefore no plant cover is presented. Investigation area in Ardu is named by region where it is situated. There the dominant plant species was Vaccinium angustifolium and accompanying species Geo-Environment, J. F. Martin-Duque, C. A. Brebbia, A. E. Godfrey & J. R. Diaz de Teran (Editors) © 2004 WIT Press, www.witpress.com, ISBN 1-85312-723-X Geo-Environment 61 were Betula sp, Eriophorum vaginatum, Salix sp., Epilobium angustifolium, Pinus sylvestris, and Calluna vulgaris. Current area is agriculturally exploited as well. Sapi-Lulli peat bog had the dominant species as Vaccinium angustifolium and in addition Pinus sp., Betula sp. and Eriophorum vaginatum. In bryophyte canopy are represented Marchantia polymorpha, Ceratodon purpureus, Polytrichum strictum, Funaria hygrometrica. Rahinge small size peat bogs, named by region were it is situated is currently agronomically exploited. The dominating plant species is Vaccinium angustifolium that is planted. Of accompanying species were presented Pinus sylvestris, Betula sp. and Eriophorum vaginatum. Tiksoja bog is classified as pine forest association Sphagno-Pinetum. The main tree species was Pinus sylvestris and some Salix sp. Accompanying species were Calluna vulgaris, Ledum palustre, Vaccinium uliginosum and Vaccinium myrtillus. From bryophytes were represented Polytrichum commune, P. strictum, Sphagnum sp. On investigation area at Emajõe dominant plant association is Salicetum cinereo-myrsinifoliae, in the bush canopy were accompanying species Salix sp., and Betula sp. In the grass canopy is presented Carex cespitosa, C. acuta, C. elata, C. nigra, C. lasiocarpa, Phragmites australis, Phalaris arundinacea, Filipendula ulmaria, Cirsium oleraceum, Potentilla palustre. On the bryophyta canopy is presented Plagiomnium ellipticum, Climacium dendroides, Calliergonella cuspidata, C. cordifolium. Table 1: Investigation areas soils and plant associations’ types. Number of investigation area 1 Investigation site 2 Ardu 3 Sapi-Lulli 4 Rahinge 5 Tiksoja 6 Emajõe Sangla Soil type Soil HSdy(fi) Plant association or dominating plant species Without plant cover V. angustifolium Fibri–Dystric Histosol Fibri–Dystric Histosol Fibri–Dystric Histosol Fibri–Dystric Histosol EndoruptiOmbric Histosol Eutri-Fluvic Histosol HSdy(fi) HSdy(fi) V. angustifolium HSdy(fi) V. angustifolium HSom Sphagno-Pinetum HSfv(eu) Salicetum cinereomyrsinifoliae For the current investigation the soil sampling was carried out in September 2003, and the plant association description during the summers of 2000 – 2003 was made. Soils were described on the basis of test pits and the samples for analysis were taken from the upper peat layer (0-20cm), the air-dried and the dry matter content was determined by drying the sample at 105 oC to the constant weight. Peat samples were analysed for organic C according to the Tjurin method [34]. For the direct estimation of the organic matter content the Geo-Environment, J. F. Martin-Duque, C. A. Brebbia, A. E. Godfrey & J. R. Diaz de Teran (Editors) © 2004 WIT Press, www.witpress.com, ISBN 1-85312-723-X 62 Geo-Environment loss-on-ignition (LOI) method [19] was used. For the determination of total N the Kjeldahl method was used [26]. Available P, K, Ca and Mg were analysed according to the Mehlich-3 method [11]. For the estimation of the microbial biomass the fumigation-extraction method was used and for the characterization of the microbial biomass activity a respiration rate was determined [29]. The mineralization of nitrogen was determined by the method of Warning and Bremner [31]. Electrical conductivity was determined in the filtered peat-water extract (1:5, v/v). The pH was measured from the soil suspension with 1M KCl (1:2,5 w/w) [26]. Water extractable organic carbon from soil-water extract (1:100, w/v) was measured [27]. The chemical oxygen demand (COD) was determined in a peat water suspension (1:100, w/v) similarly to Ranneklev & GisselrØd [27], but instead of uncreated Cr(VI) in the final solution, we determined spectrophotometrically (λ=590 nm) the amount of Cr(III), which is formed as a result of oxidation reactions and the results were reported as L O2 100g-1. For the total phosphorus determination the soil was destroyed by wet digestion and phosphorus was determined spectrophotometrically in the acid extract by vanadomolybdophosphoric acid method [19]. Based on the data of the Estonian Meteorological and Hydrological Institute. Vegetation period (181 days in 2003) was characterised by average temperatures of 13 °C and the total precipitations of 421 mm. The average temperature of many years for vegetation period was 12.2 °C. ANOVA was used for statistical analysis and standard deviation (± SD) is presented in tables. 3 Results and discussion 3.1 Soil organic matter on investigation areas The annual peat loss by mineralization in agriculturally managed peat fields can reach up to 10 – 15 t ha-2 [31]. Mineralization rate depends on cultivated species. The experimental results in Estonia showed that in the uppermost 40 cm topsoil there was peat mineralisation as much as 2.6 t ha-1 in peat soil during the cultivation of different grass species [13]. The peat CO2-C respiration is correlated positively with the increased temperature sum treatment and higher peat N amounts [12]. However, poor substrate quality limits respiration more than do low nutrient concentrations [3]. The respiration rate differed between investigation sites. It was statistically higher in the Ardu and the Tiksoja sites, 4.2 and 5.0 µg CO2 g-1 per day, respectively. In the rest of the investigation areas it ranged from 1.9 to 2.4 µg CO2 g-1 per day. The statistical analysis did not confirm the significance on the respiration rate in the Rahinge and the Emajõe flood-plain. The ash content was different between the Emajõe flood-plain (6) 31.6% and on the rest of investigation areas it ranged from 1.5 to 5.5%. The content of mineralized N was the highest in the Emajõe flood-plain 0.51 mg g-1. The next highest amount of mineralized N was found in the Tiksoja bog (0.45 mg g-1), it was confirmed with a statistical analysis. In the rest of the study sites the mineralised N differed from 0.20 to 0.25 mg g-1. Hartman et al. [12] Geo-Environment, J. F. Martin-Duque, C. A. Brebbia, A. E. Godfrey & J. R. Diaz de Teran (Editors) © 2004 WIT Press, www.witpress.com, ISBN 1-85312-723-X Geo-Environment 63 suggested that the availability of and the relationships between different N and C forms depend on the temperature sum and the peat nitrogen content. Table 2: Peculiarities of peat on the different investigation areas. Parameters of the peat quality Investigation area 1 2 3 4 5 6 Respiration, µg CO2 g-1 per day Ash content, % 2.4 ± 0.4 4.2 ± 0.4 1.9 ± 0.7 2.0 ± 1.0 5.0 ± 0.5 2.2 ± 0.2 3.6 ± 0.8 - 1.5 ± 0.1 5.5 ± 0.1 Mineralized N, mg g-1 0.24 ± 0.02 0.25 ± 0.04 0.20 ± 0.05 1.9 ± 0.03 0.21 ± 0.08 0.45 ± 0.1 31.6 ± 6.7 0.51 ± 0.03 Total biomass, mg g-1 8.6 ± 4.6 - 8.2 ± 5.7 13.5 ± 2.4 17.3 ± 5.9 6.1 ± 1.8 Biomass C, mg g-1 Biomass N, µg g-1 4.3 ± 2.3 - 4.1 ± 2.8 6.8 ± 1.2 8.6 ± 3.0 3.0 ± 0.9 642 ± 338 - 607 ± 421 1004 ± 181 1283 ± 440 451 ± 132 CWE, % 0.59 ± 0.04 0.60 ± 0.04 0.54 ± 0.31 0.25 ± 0.13 0.32 ± 0.14 0.26 ± 0.15 The C:N ratio in investigated peat soils differed significantly reaching from 10.5 in Eutri-Fluvic Histosol till 71.3 Fibri-Dystric Histosol in Ardu study site. The lower value is characteristic for a relatively stabilized soil organic matter that was characteristic to the flood plain well decomposed peat, area that is not flooded for a long time but influenced by high level of ground water [24]. Higher value of C:N relationship is characteristic for well preserved peat [35]. Water soluble peat organic carbon (CWE, %) is considered to be the most labile and mobile form of peat organic carbon. The content of water dissolved C (CWE, %) was statistically lower in the peat soils of the Rahinge and the Emajõe floodplain (0.25 and 0.26 %, respectively). In the rest of the investigation areas it was from 0.32 to 0.60 %. The chemical oxygen demand that is used for oxidation of water soluble organic material in peat soil, was in the first three study sites from 1.01 to 1.12 L O2 100g-1, in Rahinge and Tiksoja it was 0.47 and 0.6 L O2 100g-1, respectively. On the Emajõe flood-plain it was 0.48 L O2 100g-1. The agricultural use of peat soils employs drainage, leading to the aeration of the surface horizons, and fertilisation, leading to eutrophication, both of which cause a large increase in microbial decay rates [2]. If to compare the different ecosystems, then the lowest microbial biomass was found in the flood-plain Eutri-Fluvic Histosol with the lowest content of organic carbon (27.4 %). The content of total biomass reached at investigated areas up to 17.3 mg g-1 on Endorupti Ombric Histosol at undisturbed ecosystem that is covered by forest. The biomass C comprised of it 50%. There is a linear correlation between the soil microbial biomass and microbial C and N, also the respiration rates displayed similar results to the microbial biomass. The microbial biomass and the activity of microorganisms is dependent on several factors including Geo-Environment, J. F. Martin-Duque, C. A. Brebbia, A. E. Godfrey & J. R. Diaz de Teran (Editors) © 2004 WIT Press, www.witpress.com, ISBN 1-85312-723-X 64 Geo-Environment available carbon which that is the fraction of soil organic carbon that heterotrophic microorganisms can easily use as carbon and energy sources [7]. The presence of Sphagnum and its litter under decomposition, in natural peatlands, brings C available to microorganisms. Then results of the study of Croft et al [6] demonstrated that peat mining decreased bacterial population as well as the populations of hemicellulolytic and cellulolytic microorganisms of peatlands for microbial decomposition. It is known that heterotrophic microbes in soils play important roles in N dynamics, and that their metabolism is often restrained by the availability of C in the soil [7, 14]. It is mentioned in the literature that the composition and the activity of the microorganisms in natural mires depends on pH, oxygen, groundwater level, soil temperature and available nutrients. The peat soils of excavated mires may initially be regarded as biologically dead and with only slowly regaining biological activity. It has been emphasised that only by liming, fertilising and planting the dormant microflora can be reactivated [16]. The experiments made in Estonia confirm that in the case of liming the plant invasion is activated in the ombotrophic peat bog. Here the use of plant species which tolerates the high level of soil acidity and have native myhcorrhizae could be encouraged. Both, V. oxycoccus and V. angustifolium growth are dependent on native myhcorrhizae which supplies plant nutrient levels and growth rates in acid peat soils [5]. Here it is important that the organic matter returns to the soil. V. angustifolium will shed the foliage and in this way the return and the production of organic matter is guaranteed. 3.2 Nutrient pool of investigated peat soils Ombotrophic peatlands are acid wetlands (pH < 4.8) with extremely low concentrations of mineral elements [33]. The soil pH was statistically lower from our investigation area at Sangla (4.2 pHKCl) and higher in the Emajõe flood-plain (6.9 pHKCl) where the dominating soil was Eutri-Fluvic Histosol. In the rest of the investigation areas the soil acidity ranged from 2.4 to 2.9 pHKCl. The electrical conductivity was quite similar in all the investigation areas varying from 0.51 to 0.65 mS. Statistically higher electrical conductivity was found in the investigation area in the Emajõe (0.65 mS) flood-plain. The content of total N (Ntot, %) was in the first two study area soils 0.6 – 0.9 %. In the Sapi-Lulli, Rahinge and Tiksoja bogs it was from 1.0 to 1.2 %. The statistically higher content of Ntot, % was found in the soils in the Emajõe floodplain (2.6 Ntot, %). The turnover of the microbial biomass has a great importance for the availability of plant nutrients, especially for P [1]. Phosphorous is the nutrient that is transferred in negligible amounts by rain to the ecosystem in contrast to N [8]. Based on the data from Statistical Office of Estonia in the region of Ida-Virumaa the emission of nitrogen oxides from stationary sources during the last three years was in average 10, 732 t [30]. Where the emission is the highest if compared to other Estonian regions. The content of available phosphorus was very low or low for all the investigated peat soils starting from 6.8 mg kg-1 at Fibri-Dystric Histosol in Sangla without plant cover reaching to 36.7 Pavb, mg kg-1 in Sapi-Lulli covered by V. angustifolium. Jakobsen [15] found that the uptake in forms of phosphate is important for the absorption and the Geo-Environment, J. F. Martin-Duque, C. A. Brebbia, A. E. Godfrey & J. R. Diaz de Teran (Editors) © 2004 WIT Press, www.witpress.com, ISBN 1-85312-723-X Geo-Environment 65 translocation of calcium. If the normal function of a root has ceased, the active absorption of nutrients will cease too, as found in the different experiments for the adsorption and the utilization of potassium, magnesium, calcium and phosphorus. The basis of Estonian energetic and some branches of industry is the local oil shale. During the processing there is emission by the combustion devices of sulfur dioxide and the fly ash. While the calcium oxide is the dominant alkaline component constituting 30.5 % of oil shale fly ash and it is resulting in 21.8 % Ca [17]. Calcium oxide has emitted in a two different form as CaSO4 and CaCO3 [17, 25]. The content of plant available Ca and Mg had a high content. The content of plant available potassium in studied Histosols varied from medium to high. The studied level of available K showed statistically lowest content in topsoil in the Emajõe flood-plain (147.3 Kavb, mg kg-1). The research results from current study are on accordance with other results done in a past in Estonia at the well composed peat soils by Heinsalu et al [13] by them was found that the content of Kavb was 232.4 mg kg-1. Table 3: The quality of peat soils from different types of the investigation area (M±SD). Parameters of the peat soil quality Ntot, % Ptot, % Ctot, % Pavb, mg kg-1 Kavb, mg kg-1 Caavb, mg kg-1 Mgavb, mg kg-1 Investigation area 1 0.9 ± 0.1 0.03 ± 0.01 38.5 ± 4.4 6.8 ± 0.1 390 ± 2.9 11096 ± 220 1492 ± 19.3 2 0.6 ± 0.4 0.04 ± 0.01 42.8 ± 1.0 13.8 ± 0.5 726 ± 16.5 2179 ± 24 394 ± 2.4 3 1.2 ± 0.4 0.04 ± 0.01 40.5 ± 2.5 36.7 ± 6.0 444 ± 11.1 2945 ± 89 568 ± 19.1 4 1.0 ± 0.1 0.03 ± 0.01 45.1 ± 2.3 11.9 ± 0.6 387 ± 8.3 5014 ± 45 857 ± 21.9 5 6 1.0 ± 0.1 2.6 ± 0.2 0.06 ± 0 0.19 ± 0.05 41.3 27.4 ± 2.1 ± 3.5 28.4 8.5 ± 1.2 ± 0.3 547 147 ± 4.5 ± 3.3 3384 19722 ± 33 ± 623 410 793 ± 6.1 ± 12.0 *tot – total nutrients, *avb – available nutrients. 4 Conclusions The results of this study suggest that the difference of studied parameters is represented between the investigations areas. Those were caused by the diverse on investigation area soil types and exploitation. The analyses done by us showed that there was relatively high content of potassium, magnesium and calcium on the investigated Histosols. The content of Pavb was low and there was observed variability on the content of available nutrients at investigation areas. The highest level in microbial biomass was observed in the investigation area that had natural plant cover as Sphagno-Pinetum and soil type as EndoryptiOmbric Histosol. The characterisation of water and nutrient pathways in all the Geo-Environment, J. F. Martin-Duque, C. A. Brebbia, A. E. Godfrey & J. R. Diaz de Teran (Editors) © 2004 WIT Press, www.witpress.com, ISBN 1-85312-723-X 66 Geo-Environment types of wetlands is needed to improve our understanding of the process operating at all the scales in natural systems and also damaged peat lands. References [1] [2] [3] [4] [5] [6] [7] [8] [9] [10] [11] [12] [13] Amador, J.A., Jones, R.D., Nutrient limitations on microbial respiration in peat soils with different phosphorous content. Soil Biology & Biochemistry, 25, 793-801, 1993. Armentano, T.V., Menges, E.S., Patterns of change in the carbon balance of organic soil wetlands of the temperate zone. Journal of Ecology, 74, 755-774, 1986. Bridgham, S.D. & Richardson, C.J., Mechanisms controlling soil respiration (CO2 and CH4) in southern peatlands. Soil Biology and Biochemistry, 24(11), pp. 089-1099, 1992. Carlile, W.R., Horticultural developments, environmental challenges and growing media: a global perspective. Peat in Horticulture, Quality and Environmental Challenges, ed. G. Shmilewski. & L. Rochefort., Pärnu, Estonia, pp. 17 – 23, 2002. Coulart, B.L., Demchak, K. & Yang, W.Q., Effect of cultural practices on yield grown 'Bluecrop' highbush blueberries, with emphasis on mycorrhizal infection levels. Acta Horticulturae, 446, pp. 271 - 278, 1997. Croft, M., Rochefort, L. & Beauchamp, C.J., Vacuum-extraction of peatlands disturbs bacterial population and microbial biomass carbon. Applied Soil Ecology, 18, pp. 1 – 12, 2001. Davidson, E.A., Galloway, L.F., Strand, M.K., Assessing available carbon: Comparison of techniques across selected forest soils. Commun. Soil Science Plant Analysis, 18, pp. 45-64, 1987. Ellenberg, H., Mayer, R. & Schauermann, J., eds. Ökosystemforschung. Ergebnisse des Sollingprojects 1966-1986. Ulmer, Stuttgart, 1986. Gorham, E., Northern peatlands: role in the carbon cycle and probable responses to climatic warming. Ecological Applications, 1, pp. 182-95, 1991. Göttlich, K. (ed.) Moor- und Torfkunde. E. Schweizerbart’sche Verlagsbuchhandlung, Stuttgart, 1990, pp. 334-349. Handbook on Reference Methods for Soil Analysis.. Soil and Plant Analysis Council, Inc. 202 pp, 1992. Hartman, M., Karsisto, M. & Sarjala, T., Microbial activity, CO – C and organic and inorganic compounds in peat during four temperature sum treatments. Ecohydrological Processes in Northern Wetlands. ed, A. Järvet & E. Lode, Tartu University Press, Tartu-Tallinn, pp 143 – 148, 2003. Heinsalu, H., Niine, H. & Veber, K. The influence of amelioration on the properties of peat soil. Estonian soils their reclamation and fertilization. Transactions of EMTUI, LXX, pp, 32-41, 1992. Geo-Environment, J. F. Martin-Duque, C. A. Brebbia, A. E. Godfrey & J. R. Diaz de Teran (Editors) © 2004 WIT Press, www.witpress.com, ISBN 1-85312-723-X Geo-Environment [14] [15] [16] [17] [18] [19] [20] [21] [22] [23] [24] [25] [26] [27] [28] [29] 67 Johnson, D.W., Cheng, W. & Burke, I.C., Biotic and abiotic nitrogen retentionin a variety of forest soils. Soil Science Society of America Journal, 64:1503-1514, 2000. Jakobsen, S. T., Interaction between Plant Nutrients. IV. Interaction between Calcium and Phosphate. Acta Agric. Scan, 43, pp. 6-10, 1993. Künnis, K., Vask, K., Lode, E. & Lundin. L., The peat profile microbiology. Ecohydrological Processes in Northern Wetlands, ed. A. Järvet, & E. Lode, Tartu University Press, Tartu-Tallinn, pp. 160 – 165, 2003. Kaasik, M. & Sõukand, Ü., Balance of alkaline and acidic pollution loads in the area affected by oil shale combustion. Oil Shale, 17(2), pp. 113128, 2000. Lavoie, C., Rochefort, L., The natural re-vegetation of a harvested peatland in southern Québec: a spatial and dendroecological analysis. Ecoscience, 3, pp. 101–111, 1996. Methods of soil analysis. Part 3. SSSA Book Series: 5, Madison, Wisconsin, USA, pp, 1390, 1996. Noormets, M. & Karp, K., The influence of fertilization to vegetative growth of the lowbush blueberry (Vaccinium angustifolium Ait.) in a young and cropping plantation in peat bog. Transactions of the Estonian Agricultural University, 212, pp. 149 - 154, 2001. Noormets, M., Karp, K. & Paal, T., Recultivation of opencast peat pits with Vaccinium culture in Estonia. Ecosystems and Sustainable Development IV, eds. E. Tiezzi, & C.A., Brebbia, Wessex Institute of Technology, UK and J-L. USO, Universitat Jaume I, Spain, 2, pp, 584, 2003. Orru, M., Širkova, M. & Veldre, M., Estonian peat resources. Estonian Geological Survey, Tallinn, pp. 146, 1992. Paal, J., Classification of Estonian vegetation site types. University of Tartu, Institute of Botany and Ecology, Tallinn, 297 pp, 1997. Paul, E.A. & Clark, F.E., Soil microbiology and biochemistry. Academic Press, London, San Diego, pp. 145-148, 1996. Pets, L.I., Vaganov, P.A., Knoth, I., Haldna, Ü., Schwenke, H., Schnier, C. & Juga, R., Microelements in oil shale ash of the Baltic Thermoelectric Power Plant. Oil Shale, 2(4), pp. 379–390, 1985. Procedures for soil analysis, ed. L.P. van Reeuwijk Wagening: ISRIC, pp, 112, 1995. Ranneklev, S.B. & Gislerød, H.R. Horticultural peat-detection of selfheating. Peat in Horticulture, Quality and Environmental Challenges, ed. G. Shmilewski. & L. Rochefort, Pärnu, Estonia, pp. 135-141, 2002. Raudsepp, R., Räägel, V., Savitskaja, L., Orru, M. & Kattai, V., Treasures of the Estonian soils. Estonian Geological Survey, Valgus, Tallinn, pp. 64, 1995. Soil Science. Methods and application, ed. D.L. Rowell, Pearson Education, pp. 350, 1994. Geo-Environment, J. F. Martin-Duque, C. A. Brebbia, A. E. Godfrey & J. R. Diaz de Teran (Editors) © 2004 WIT Press, www.witpress.com, ISBN 1-85312-723-X 68 Geo-Environment [30] [31] [32] [33] [34] [35] Statistical Yearbook 2002, Statistical Office of Estonia, Estonia, Tallinn, pp. 123, 2003. Tomberg, U., Breakdown of peat as a result of drainage. Estonia, Saku, pp. 32, 1992. Waring, S.A. & Bremner, J.M. Ammonium production in soil under waterlogged conditions as an index of nitrogen availability. Nature, 201, pp. 951-952, 1964. Vitt, D.H. & Chee, W.L., The relationships of vegetation to surface water chemistry and peat chemistry in fens of Alberta, Canada. Vegetation, 89, pp. 87-106, 1990. Vorobjova, L.A., Chemical analysis of soils. Textbook, Moscow University Press, pp. 272, 1998. Zupančič, M. & Mahne, I., Effect of environmental factors on the capacity for carbon and nitrogen mineralisation in peat soil. Proc. of 2nd Congress of Slovenian microbiologists, Portorož, Slovenija, Slovene Microbiological Society, pp. 209-212, 1998. Geo-Environment, J. F. Martin-Duque, C. A. Brebbia, A. E. Godfrey & J. R. Diaz de Teran (Editors) © 2004 WIT Press, www.witpress.com, ISBN 1-85312-723-X
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