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  • 1
    ISSN: 1432-0789
    Keywords: Key words Dissolved organic nitrogen ; Soluble organic nitrogen ; Nitrogen transformations ; Nitrogen loss ; Leaching
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Geosciences , Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract  The existence of soluble organic forms of N in rain and drainage waters has been known for many years, but these have not been generally regarded as significant pools of N in agricultural soils. We review the size and function of both soluble organic N extracted from soils (SON) and dissolved organic N present in soil solution and drainage waters (DON) in arable agricultural soils. SON is of the same order of magnitude as mineral N and of equal size in many cases; 20–30 kg SON-N ha–1 is present in a wide range of arable agricultural soils from England. Its dynamics are affected by mineralisation, immobilisation, leaching and plant uptake in the same way as those of mineral N, but its pool size is more constant than that of mineral N. DON can be sampled from soil solution using suction cups and collected in drainage waters. Significant amounts of DON are leached, but this comprises only about one-tenth of the SON extracted from the same soil. Leached DON may take with it nutrients, chelated or complexed metals and pesticides. SON/DON is clearly an important pool in N transformations and plant uptake, but there are still many gaps in our understanding.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Soil use and management 2 (1986), S. 0 
    ISSN: 1475-2743
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Geosciences , Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract Soil samples have been taken periodically from unlimed plots of the 130-year-old Park Grass Experiment and from the 100-year-old Geescroft Wilderness at Rothamsted. Changes in the pH of the samples show how acidification has progressed. The soils are now at, or are approaching, equilibrium pH values which depend on the acidifying inputs and on the buffering capacities of the soils. We have calculated the contributions to soil acidification of natural sources of acidity in the soil, atmospheric deposition, crop growth and nutrient removal, and, where applicable, additions of fertilizers. The relative importance of each source of acidification has changed as the soils have become more acid. Acid rain (wet deposited acidity) is a negligible source, but total atmospheric deposition may comprise up to 30% of acidifying inputs at near neutral soil pH values and more as soil pH decreases. Excepting fertilizers, the greatest causes of soil acidification at or near neutral pH values are the natural inputs of H+ from the dissolution of CO2 and subsequent dissociation of carbonic acid, and the mineralization of organic matter.Under grassland, single superphosphate and small amounts of sodium and magnesium sulphates have had no effect on soil pH, whilst potassium sulphate increased soil acidity slightly. All of these effects are greatly outweighed under grassland, however, by those of nitrogen fertilizers. Against a background of acidification from atmospheric, crop and natural inputs, nitrogen applied as ammonium sulphate decreased soil pH up to a maximum of 1.2 units at a rate in direct proportion to the amount added, and nitrogen applied as sodium nitrate increased soil pH by between 0.5 and 1 unit.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Soil use and management 1 (1985), S. 0 
    ISSN: 1475-2743
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Geosciences , Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract. Rainfall has become less acid at Rothamsted and Saxmundham over the period 1969–83. The pH of rain at these two sites has increased from 4.4–4.6 to about 4.8–4.9; at Woburn it has remained approximately constant at 4.4–4.6. Amounts of NH4-N and NO3-N deposited at present are 10–15 and 5–10 kg ha−1 a−1 respectively. They have been increasing at Rothamsted and Woburn. Some 50–60 kg ha−1 a−1 of Cl and 25–35 kg ha−1 a−1 of SO4-S are presently deposited. Deposition of non-sea Cl and SO4-S has been increasing markedly at all three sites. Non-sea salts comprise 35% of the total salt deposition near the coast at Saxmundham, 58% inland at Rothamsted and Woburn.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Science Ltd
    Global change biology 9 (2003), S. 0 
    ISSN: 1365-2486
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology , Energy, Environment Protection, Nuclear Power Engineering , Geography
    Notes: The accumulation of carbon (C) and nitrogen (N) was measured on two sites on Rothamsted Farm that had been fenced off some 120 years ago and allowed to revert naturally to woodland. The sites had previously been arable for centuries. One had been chalked and was still calcareous; the other had never been chalked and the pH fell from 7.1 in 1883 to 4.4 in 1999. The acidic site (Geescroft wilderness) is now a deciduous wood, dominated by oak (Quercus robor); the calcareous site (Broadbalk wilderness) is now dominated by ash (Fraxinus excelsior), with sycamore (Acer pseudoplatanus) and hawthorn (Craetagus monogyna) as major contributors. The acidic site gained 2.00 t C ha−1 yr−1 over the 118-year period (0.38 t in litter and soil to a depth of 69 cm, plus an estimated 1.62 t in trees and their roots); the corresponding gains of N were 22.2 kg N ha−1 year−1 (15.2 kg in the soil, plus 6.9 kg in trees and their roots). The calcareous site gained 3.39 t C ha−1 year−1 over the 120-year period (0.54 t in the soil, plus an estimated 2.85 t in trees and roots); for N the gains were 49.6 kg ha−1 yr−1 (36.8 kg in the soil, plus 12.8 kg in trees and roots). Trees have not been allowed to grow on an adjacent part of the calcareous site. There is now a little more C and N in the soil from this part than in the corresponding soil under woodland. We argue from our results that N was the primary factor limiting plant growth and hence accumulation of C during the early stages of regeneration in these woodlands. As soil organic N accumulates and the sites move towards N saturation, other factors become limiting. Per unit area of woodland, narrow strips; that is, wide hedges with trees, are the most efficient way of sequestering C – provided that they are not short of N.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1365-2486
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology , Energy, Environment Protection, Nuclear Power Engineering , Geography
    Notes: Increases in the long-range aerial transport of reactive N species from low to high latitudes will lead to increased accumulation in the Arctic snowpack, followed by release during the early summer thaw. We followed the release of simulated snowpack N, and its subsequent fate over three growing seasons, on two contrasting high Arctic tundra types on Spitsbergen (79°N). Applications of 15N (99 atom%) at 0.1 and 0.5 g N m−2 were made immediately after snowmelt in 2001 as either Na15NO3 or 15NH4Cl. These applications are approximately 1 × and 5 × the yearly atmospheric deposition rates. The vegetation at the principal experimental site was dominated by bryophytes and Salix polaris while at the second site, vegetation included bryophytes, graminoids and lichens. Audits of the applied 15N were undertaken, over two or three growing seasons, by determining the amounts of labeled N in the soil (0–3 and 3–10 cm), soil microbial biomass and different vegetation fractions.Initial partitioning of the 15N at the first sampling time showed that ∼60% of the applied 15N was recovered in soil, litter and plants, regardless of N form or application rate, indicating that rapid immobilization into organic forms had occurred at both sites. Substantial incorporation of the 15N was found in the microbial biomass in the humus layer and in the bryophyte and lichen fractions. After initial partitioning there appeared to be little change in the total 15N recovered over the following two or three seasons in each of the sampled fractions, indicating highly conservative N retention. The most obvious transfer of 15N, following assimilation, was from the microbial biomass into stable forms of humus, with an apparent half-life of just over 1 year. At the principal site the microbial biomass and vascular plants were found to immobilize the greatest proportion of 15N compared with their total N concentration. In the more diverse tundra of the second site, lichen species and graminoids competed effectively for 15NH4-N and 15NO3-N, respectively. Results suggest that Arctic tundra habitats have a considerable capacity to immobilize additional inorganic N released from the snow pack. However, with 40% of the applied 15N apparently lost there is potential for N enrichment in the surrounding fjordal systems during the spring thaw.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Science Ltd
    European journal of soil science 51 (2000), S. 0 
    ISSN: 1365-2389
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Geosciences , Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: The usefulness of stored soils from long-term experiments is often questioned because of changes that might occur during storage. We examined changes during long-term storage (8–69 years) in the chemical properties of soils with a range of pH values (3.4–8.1 in water) from woodland and grassland experiments at Rothamsted Experimental Station in the UK. No significant changes during storage were measured for total C and N. Large but erratic changes in exchangeable Na+ content between 1959 and 1991 were probably caused by contamination of the 1959 samples by perspiration and from sodium-based glassware. Exchangeable K+ increased during storage but only by a small amount. Small changes in exchangeable Ca2+ and Mg2+ were measured in some samples but not in others. Generally the amount of exchangeable cations increased slightly during storage. This is probably linked to the decreases of 〈inlineGraphic alt="leqslant R: less-than-or-eq, slant" extraInfo="nonStandardEntity" href="urn:x-wiley:13510754:EJSS307:les" location="les.gif"/〉 0.4 units in the pH of acid soils, which we attribute to the hydrolysis of approximately 0.25% of the exchangeable Al3+. A doubling of the amount of exchangeable Mn2+ during storage for 32 years was probably caused by re-equilibration of Mn species. The most practicable way to prepare soil samples for long-term storage is to dry them in air. However, those who study changes in soil by re-analysing samples of the soil stored for a long time must (i) use the same methods of analysis, or (ii) demonstrate that different methods lead to the same results, and (iii) know what changes can arise during storage.
    Type of Medium: Electronic Resource
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