Nitrification and organic nitrogen formation in soils

Summary The formation of mineral nitrogen species and of organic nitrogen was studied in three different types of soils in relation to the application of the nitrification inhibitor nitrapyrin. The results indicate that nitrification brings about a deficit in total mineral nitrogen and a concomitant surplus in non biomass organic nitrogen. This phenomenon increases with increasing levels of applied ammonium nitrogen and soil organic matter. The phenomenon is considered to be due to the reaction of the transient nitrite formed with soil phenolic compounds and appears to be of significance in all soils in which nitrification occurs, even neutral to alkaline and low carbon soils.     

Influence of different organic waste materials on the transformation of nitrogen in soils

Organic waste materials like crop residues, well-decomposed cow dung, composts, and other rural and urban wastes are considered highly useful resources in enhancing soil fertility and also in build-up of soil organic matter. Organic matter decomposition provides plant nutrients in soil, which in turn increases crop productivity. Availability of nutrients and nitrogen (N) and phosphorus from organic waste materials is dependent upon the nature of organic residues, climatic conditions, and soil moisture activity. Keeping these factors in view, the present investigation was undertaken to study the transformation of N from different organic waste materials in two contrasting soils from an eastern India, subtropical region. The results showed that the amounts of ammoniacal-N (NH4-N), nitrate-N (NO3-N), hydrolysable N (HL-N), and nonhydrolysable (NHL-N) were increased for up to 60 days of soil submergence and increased further with the increase (1% by weight of soil) of organic residue application. Considering the effect of various organic waste materials, it was found that the amounts of NH4-N, NO3-N, HL-N, and NHL-N were higher with the application of groundnut hull as compared to wheat straw and potato skin, which may be due to relatively narrow carbon:N ratio of groundnut (22:43) than that of wheat straw (62:84) and potato skin (71:32); however, the results showed that the release of NH4-N, NO3-N, HL-N, and NHL-N was in the order of groundnut hull > wheat straw > potato skin.     

Turnover of organic nitrogen in soils and its availability to crops

The root development of barley seedlings grown for one week in an aerated nutrient solution was studied in the presence of dissolved organic matter from an aqueous chestnut leaf litter extract. In particular, the different effects of low and high molecular weight fractions (small molecules: molecular weight <1000; large molecules: >10,000) of the leaf litter extract were examined. In the presence of large molecules root growth was inhibited, an irregular root tip morphology was observed, and Ca and Mg concentrations in the shoots were lower than in control plants. These phytotoxic effects were not caused by the formation of an impermeable layer of large molecules on the root surfaces that lower accessibility for nutrient cations as inferred from voltammetric experiments. A germination assay using spruce seeds, however, indicated allelochemical effects of large molecules, which exhibit a higher aromaticity than the small molecules as indicated by spectroscopic characterisation. In the growth experiments with small molecules, no influence on the root development of barley was evident, but an increase of Ca and Mg in the shoots was detected. During these growth experiments, a large amount of the small molecules, mainly simple phenols and amino acids, disappeared from the nutrient solution. The loss of small molecules was most likely the effect of mineralisation.Abbreviations DOC dissolved organic carbon - DOM dissolved organic matter - LLE leaf litter extract - MW molecular weight - HMDE hanging mercury drop electrode     

Contribution of amino compounds to dissolved organic nitrogen in forest soils

Dissolved organic nitrogen (DON) may play an important role in plantnutrition and nitrogen fluxes in forest ecosystems. In spite of the apparentimportance of DON, there is a paucity of information concerning its chemicalcomposition. However, it is exactly this chemical characterization that isrequired to understand the importance of DON in ecosystem processes. Theprimaryobjective of this study was to characterize the distribution of free aminoacidsand hydrolyzable peptides/proteins in the DON fraction of Oa horizon leachatesalong an extreme edaphic gradient in northern California. Insitu soil solutions were extracted by centrifugation from Oahorizonscollected beneath Pinus muricata (Bishop pine) andCupressus pygmaea (pygmy cypress) on slightlyacidic/fertile and highly acidic/infertile sites. DON accounted for 77 to99% of the total dissolved nitrogen in Oa horizon leachates. Nitrogen infree amino acids and alkyl amines ranged from 0.04–0.07 mgN/L on the low fertility site to 0.45–0.49 mg N/L onthe high fertility site, and accounted for 1.5 to 10.6% of the DON fraction.Serine, glutamic acid, leucine, ornithine, alanine, aspartic acid andmethylamine were generally the most abundant free amino compounds. Combinedamino acids released by acid hydrolysis accounted for 48 to 74% of theDON, suggesting that proteins and peptides were the main contributor to DON inOa horizon leachates. Together, nitrogen from free andcombined amino compounds accounted for 59 to 78% of the DON. Most of theDON was found in the hydrophobic fraction, which suggests the presence ofprotein/peptide-polyphenol complexes or amino compounds associated withhumic substances. Because free and combined amino acids can be an importantnitrogen source for some plants, soil DON may play an important role in plantnutrition and ecosystem function.     

不同类型农田土壤对可溶性有机氮、碳的吸附特性

研究了陕西关中地区红油土和淋溶褐土耕层土壤对分离的有机肥提取液中可溶性有机氮、碳(SON和SOC)的吸附特性.结果表明:原始物质吸附等温线方程可以反映土壤对可溶性有机氮、碳的吸附特性,土壤吸附SON、SOC的数量与它们各自加入的量呈极显著线性关系.从原始物质吸附等温线方程的分配系数m看,淋溶褐土对SON、SOC的吸附能力强于红油土.红油土对SON、SOC的平均吸附率分别为24.3%和18.8%,淋溶褐土则分别为38.3%和18.6%;两种类型土壤对SON和SOC的吸附能力较低,说明它们在土壤中具有较强的移动性;土壤对SOC的吸附能力弱于SON,说明SOC更易于从土壤中流失.     

Carbon,nitrogen and phosphorus concentrations in aggregates of organic waste-amended soils

This study was undertaken to evaluate the long-term effects of organic wastes on dry aggregate size distribution and on the C, N and available-P concentrations within the different aggregate fractions of some agricultural soils in North-Central Italy. Topsoils (0–20 cm) which had been amended for several years with either pig slurry (PS), cattle slurry (CS) or sewage sludge (SS) were separated into four macro-aggregate classes (4-2, 2-1, 1-0·5, 0·5-0·25 mm) and three micro-aggregate classes (0·25-0·125, 0·125-0·05 and < 0·05 mm) by dry sieving. Compared with the unamended soils, there was generally a slight increase in the proportion of the 4-2 mm macro-aggregate class following waste application. Irrespective of treatment, macro-aggregates (>0·25 mm) constituted > 70% of the total aggregate fractions.Average increases of 17, 13 and 67% (organic C), 18, 13 and 57% (total N) and 430, 372 and 642% (available P) were obtained from additions of PS, CS and SS, respectively, and increases were found in all aggregate fractions following waste application. There was a close positive correlation between the concentrations of C, N and to a lesser extent P, in the aggregates and their silt-plus-clay contents. In terms of total contents, these elements were preferentially concentrated in the macro-aggregates. Only slight differences in the C/N ratios of the aggregates were observed but their C/P and N/P ratios decreased significantly (P ≤ 0·05) following waste application.     

黄土区不同类型土壤可溶性有机氮的含量及特性

测定了黄土高原地区不同生态系统土壤中可溶性有机氮（SON）和游离氨基酸的含量,并分析了其与土壤其他性质之间的关系。结果表明,黑垆土、红油土和淋溶褐土中SON的平均含量分别为24．75、39．10mg／kg和41．80mg／kg,占可溶性总氮（TSN）的51．25％、68．28％和68．57％,分别为土壤全氮的2．54％、3．75％和4．00％;土壤游离氨基酸的含量分别为7．18、7．42mg／kg和7．41mg／kg,分别占SON的30．53％、19．23％和17．50％,占全氮的0．74％、0．71％和0．71％．方差分析结果表明,土壤类型对土壤SON含量及其在TSN和全氮中所占的比例、游离氨基酸在SON中所占的比例有显著影响,而对游离氨基酸的含量及其占土壤全氮比例的影响未达显著水平。枯枝落叶层中SON含量（248．26mg／kg）为农田土壤（24．75mg／kg）的10倍左右,且林地土壤0～20cm土层SON含量（31．03mg／kg）显著的高于当地农田,两种生态系统0～20cm土层土壤中游离氨基酸含量（7．18～7．32mg／kg）相当,但均极显著低于枯枝落叶层中游离氨基酸平均含量（18．57mg／kg）。相关分析结果表明,TSN、SON以及游离氨基酸与全氮、硝态氮、铵态氮、有机质等各养分之间均有极显著的相关性。     

The cycling of organic nitrogen through the atmosphere

Atmospheric organic nitrogen (ON) appears to be a ubiquitous but poorly understood component of the atmospheric nitrogen deposition flux. Here, we focus on the ON components that dominate deposition and do not consider reactive atmospheric gases containing ON such as peroxyacyl nitrates that are important in atmospheric nitrogen transport, but are probably not particularly important in deposition. We first review the approaches to the analysis and characterization of atmospheric ON. We then briefly summarize the available data on the concentrations of ON in both aerosols and rainwater from around the world, and the limited information available on its chemical characterization. This evidence clearly shows that atmospheric aerosol and rainwater ON is a complex mixture of material from multiple sources. This synthesis of available information is then used to try and identify some of the important sources of this material, in particular, if it is of predominantly natural or anthropogenic origin. Finally, we suggest that the flux of ON is about 25 per cent of the total nitrogen deposition flux.     

The retention of organic matter in soils

The turnover of C in soils is controlled mainly by water regimes and temperature, but is modified by factors such as size and physicochemical properties of C additions in litter or root systems, distribution of C throughout the soil as root systems, or addition as litter, distribution of C within the soil matrix and its interaction with clay surfaces.Soil factors which retard mineralization of C in soils are identified from correlations of C contents of soils with other properties such as clay content and base status. The rate and extent of C mineralization depends on the chemistry of the added organic matter and interaction with clays of the microbial biomass and metabolites.The organomineral interactions are shown to depend on cation bridges involving mainly Ca in neutral to alkaline soils, Al in acid soils and adsorption of organic materials on iron oxide surfaces. The various organomineral interactions lead to aggregations of clay particles and organic materials, which stabilizes both soil structure and the carbon compounds within the aggregates.     

Enzymology under global change: organic nitrogen turnover in alpine and sub-Arctic soils

Understanding global change impacts on the globally important carbon storage in alpine, Arctic and sub-Arctic soils requires knowledge of the mechanisms underlying the balance between plant primary productivity and decomposition. Given that nitrogen availability limits both processes, understanding the response of the soil nitrogen cycle to shifts in temperature and other global change factors is crucial for predicting the fate of cold biome carbon stores. Measurements of soil enzyme activities at different positions of the nitrogen cycling network are an important tool for this purpose. We review a selection of studies that provide data on potential enzyme activities across natural, seasonal and experimental gradients in cold biomes. Responses of enzyme activities to increased nitrogen availability and temperature are diverse and seasonal dynamics are often larger than differences due to experimental treatments, suggesting that enzyme expression is regulated by a combination of interacting factors reflecting both nutrient supply and demand. The extrapolation from potential enzyme activities to prediction of elemental nitrogen fluxes under field conditions remains challenging. Progress in molecular '-omics' approaches may eventually facilitate deeper understanding of the links between soil microbial community structure and biogeochemical fluxes. In the meantime, accounting for effects of the soil spatial structure and in situ variations in pH and temperature, better mapping of the network of enzymatic processes and the identification of rate-limiting steps under different conditions should advance our ability to predict nitrogen fluxes.     

Distribution of organic carbon and nitrogen in surface soils in the McMurdo Dry Valleys, Antarctica

The organic carbon and nitrogen contents of sediments in the upper 2 cm of the soils surrounding several lakes in the McMurdo Dry Valleys were measured in a relatively high-density sampling grid, in order to better understand the present-day distribution of organic matter in the ecosystem that is most readily transportable via aeolean processes. Carbon and nitrogen contents of the bulk sediments and size-differentiated sediments decreased in a series according to lake basins oriented along the Taylor Valley's main axis (Lake Fryxell > Hoare ≥ west lobe Bonney ≥ east lobe Bonney). Samples were also obtained around Lake Vida and showed this basin to contain less organic matter than those in the Taylor Valley. This regional spatial analysis supports the emerging view that each basin provides distinct environments for in situ microbial activity, lithogenic weathering, aeolian deposition and sorting that can be detected through synoptic sampling. Accepted: 2 August 1999     

How does fire affect the nature and stability of soil organic nitrogen and carbon? A review

After vegetation fires considerable amounts of severely or partly charred necromass (referred to here as char) are incorporated into the soil, with long-term consequences for soil C and N dynamics and thus N availability for primary production and C and N transport within the soil column. Considering results reported in the pyrolysis literature in combination with those obtained from controlled charring of plant material and soil organic matter (SOM), it has become clear that common models claiming char as a graphite-like material composed mainly of highly condensed polyaromatic clusters may be oversimplified. Instead, I suggest a concept in which char is a heterogeneous mixture of heat-altered biopolymers with domains of relatively small polyaromatic clusters, but considerable substitution with N, O and S functional groups. Such a concept allows fast oxidation facilitating both microbial attack and dissolution. Although, char is commonly believed to degrade more slowly than litter, over the long term and under oxic conditions, char may degrade to an extent that it becomes indistinguishable from naturally formed SOM. Oxygen depletion or environments with low microbial activity may be necessary for char to survive without major chemical alteration and in considerable amounts for millennia or longer.     

The fate of15N-labelled organic nitrogen in sheep manure applied to soils of different texture under field conditions

The fate of nitrogen from¹⁵N-labelled sheep manure and ammonium sulfate in small lysimeters and plots in the field was studied during two growth seasons. In April 1991,¹⁵N-labelled sheep faeces (87 kg N ha^–1) plus unlabelled (NH₄)₂SO₄ (90 kg N ha^–1), and (¹⁵NH₄)₂SO₄ (90 kg N ha^–1) were each applied to three soils; soil 1 (100% soil + 0% quartz sand), soil 2 (50% soil + 50% quartz sand) and soil 3 (25% soil + 75% quartz sand). The lysimeters were cropped with spring barley (Hordeum vulgare L.) and undersown ryegrass (Lolium perenne L.). The barley crop recovered 16–17% of the labelled manure N and 56% of the labelled (NH₄)₂SO₄-N. After 18 months 30% of the labelled manure N and 65% of the labelled (NH₄)₂SO₄-N were accumulated in barley, the succeeding ryegrass crop and in leachate collected below 45 cm of soil, irrespective of the soil-sand mixture. Calculating the barley uptake of manure N by difference of N uptake between manured and unmanured soils, indicated that 4%, 10% and 14% of the applied manure N was recovered in barley grown on soil-sand mixtures with 16%, 8% and 4% clay, respectively. The results indicated that the mineralization of labelled manure N was similar in the three soil-sand mixtures, but that the manure caused a higher immobilization of unlabelled ammonium-N in the soil with the highest clay content. Some of the immobilized N apparently was remineralized during the autumn and the subsequent growth season. After 18 months, 11–19% of the labelled manure N was found in the subsoil (10–45 cm) of the lysimeters, most of this labelled N probably transported to depth as organic forms by leaching or through the activities of soil fauna. In unplanted soils 67–74% of the labelled manure N was recovered in organic form in the 0–10 cm soil layer after 4 months, declining to 55–64% after 18 months. The lowest recovery of labelled N in top-soil was found in the soil-sand mixture with the lowest clay content. The mass balance of¹⁵N showed that the total recovery of labelled N was close to 100%. Thus, no significant gaseous losses of labelled N occurred during the experiment.     

The nature of three ancient woodland soils in southern England

Abstract. Despite a wealth of published research on the nature of woodland soils, little is known about the nature of soils on sites that have supported woodland for many hundreds of years, namely ancient woodland. The properties and variability of soils in three ancient woods; one in the New Forest, Hampshire and two in Berkshire, were compared with those under recent woods. The acidity of ancient and recent woodland soils was high and remarkably similar. Only where cultivation of soils had preceded woodland establishment was soil acidity lower. The quantity of carbon in the soils studied was inversely related to soil acidity and the ancient woods had accumulated larger quantities of carbon than their recent counterparts. The quantities of Ca²⁺, Mg²⁺ and K⁺ were larger in the ancient woods except where prior cultivation had taken place. Total and organic phosphate contents of the ancient woodland soils were also consistently larger. The nature and pattern of soil variability in ancient woodland soils was quite distinct from that found in recent woods. Overall, the variability of soil acidity, carbon content and organic phosphate was larger in the ancient woodland soils but the pattern of variability differed between the soil properties. No clear association existed between the pattern of soil acidity and individual trees. At the surface of some of the woodland soils, however, carbon distribution appeared to be associated with individual trees. At depth in the ancient woodland soils, the association with the existing vegetation cover was not so clear. It is probable that the ancient woodland soils retained relict features of previous vegetation cover. Organic phosphate distribution was very strongly associated with the present vegetation cover. The pattern of distribution of organic phosphate appeared to be stronger than that of soil acidity and carbon content.     

Abiotic factors regulating nitrogen transformations in the organic layer of acid forest soils: Moisture and pH

The relationships between nitrogen transformations and moisture and pH in coniferous forest litter were determined using laboratory incubation experiments. A linear relation between gravimetric moisture content and nitrification was found within the whole studied range of moisture conditions (10–290% ODW). Net nitrogen mineralization increased linearly with moisture content up to 140% ODW. At higher moisture contents, net mineralization was found to be independent of moisture. Relative nitrification was found to be a linear function of moisture content. The dependence of the CO₂ production rates on moisture in the coniferous litter decreased from low to high moisture availability. Due to a nearly linear relationship between gravimetric moisture content and log-(water potential) within the investigated moisture range, the same type of relationships were found with this latter parameter as well. The relationship between nitrogen transformations and pH was studied by means of the addition of different amounts of HCl and NaOH during short incubation experiments (1 week). Nitrification was found to be a negative linear function of the H-ion concentration within the range of 0.04 (pH 4.40) and 0.36 (pH 3.45) mmol H-ion L^?1. At a higher H-ion concentration and thus at a lower pH than 3.45, no nitrate was produced any more. No relationship between net mineralization and pH was found.     

The nature and distribution of various forms of nitrogen in the potato

The distribution of nitrogen fractions in the organs of King Edward potato plants harvested at intervals during the growing season has been determined. A general picture of the nitrogen distribution is presented and certain problems suggested by the data are discussed.
Each organ of the plant shows a uniformity in its nitrogenous composition during the whole season of active growth. The seed tubers are characterized by their high content of non-protein nitrogen. This fraction yields the greater part of the nitrogen withdrawn from the seed tubers; the amide, amino and 'other nitrogen' fractions all being markedly depleted. The severely depleted tubers retain some 20% of their initial nitrogen content.
The roots are rich in non-protein nitrogen, in which nitrate nitrogen is an important fraction. The roots from ammonium sulphate-treated plots had a higher total nitrogen content than those from untreated plots, due to accumulation of ammonia nitrogen.
The 'tops' have a higher nitrogen content and a higher proportion of protein than the roots. There is an increase in protein content and a decrease in non-protein nitrogen in passing from stems, to petioles, to leaf laminae. The depleted tubers and roots and stems have a uniform low-protein content of the order 0.4-0.6 mg. protein nitrogen per g. fresh weight.
Asparagine and glutamine occur in approximately equal amounts in the seed tubers and roots. Glutamine is more completely withdrawn than asparagine from the tubers, and in the 'tops' it constantly exceeds asparagine in amount.
A study of the concentration gradients, from leaves to petioles, to stems, to stem bases and new tubers, of the fractions of the non-protein nitrogen focuses attention upon the 'other nitrogen' as containing the organic nitrogen most actively involved in translocation.
The concentration and total content of the glycoside solanine in the different organs has been determined at each sampling.     

The carbon bonus of organic nitrogen enhances nitrogen use efficiency of plants

The importance of organic nitrogen (N) for plant nutrition and productivity is increasingly being recognized. Here we show that it is not only the availability in the soil that matters, but also the effects on plant growth. The chemical form of N taken up, whether inorganic (such as nitrate) or organic (such as amino acids), may significantly influence plant shoot and root growth, and nitrogen use efficiency (NUE). We analysed these effects by synthesizing results from multiple laboratory experiments on small seedlings (Arabidopsis, poplar, pine and spruce) based on a tractable plant growth model. A key point is that the carbon cost of assimilating organic N into proteins is lower than that of inorganic N, mainly because of its carbon content. This carbon bonus makes it more beneficial for plants to take up organic than inorganic N, even when its availability to the roots is much lower – up to 70% lower for Arabidopsis seedlings. At equal growth rate, root:shoot ratio was up to three times higher and nitrogen productivity up to 20% higher for organic than inorganic N, which both are factors that may contribute to higher NUE in crop production.