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1.
Meeting the goal of long-term agricultural productivity requires that soil degradation be halted and reversed. Soil fertility decline is a key factor in soil degradation and is probably the major cause of declining crop yields. There is evidence that the contribution of declining soil fertility to soil degradation has been underestimated. <br>Sensitivity to soil degradation is implicit in the assessment of the sustainability of land management practices, with wide recognition of the fact that soils vary in their ability to resist change and recover subsequent to stress. The concept of resilience in relation to sustainability requires further elaboration and evaluation.<br>In the context of soil degradation, a decline in soil fertility is primarily interpreted as the depletion of organic matter and plant nutrients. Despite a higher turnover rate of organic matter in the tropics there is no intrinsic difference between the organic matter content of soils from tropical and temperate regions. The level of organic matter in a soil is closely related to the above and below ground inputs. In the absence of adequate organic material inputs and where cultivation is continuous, soil organic matter declines progressively. Maintaining the quantity and quality of soil organic matter should be a guiding principle in developing management practices.<br>Soil microbial biomass serves as an important reservoir of nitrogen (N), phosphorus (P) and sulphur (S), and regulates the cycling of organic matter and nutrients. Because of its high turnover rate, microbial biomass reacts quickly to changes in management and is a sensitive indicator for monitoring and predicting changes in soil organic matter. Modelling techniques have been reasonably successful in predicting changes in soil organic matter with different organic material inputs, but there is little information from the tropics. <br>Nutrient depletion through harvested crop components and residue removal, and by leaching and soil erosion accentuates the often very low inherent fertility of many soils in the tropics. An integrated approach involving inorganic and organic inputs is required where animal and plant residues are returned, as far as practicable. Chemical fertilizers alone cannot achieve long-term productivity on many soils and organic material inputs are required to maintain soil organic matter levels and crop productivity. A major research effort is required to develop improved strategies for halting and reversing soil degradation if long-term productivity is to be secured. <br>  相似文献   

2.
Biomass production of annual crops is often directly proportional to the amounts of radiation intercepted, water transpired and nutrients taken up. In many places the amount of rainfall during the period of rapid crop growth is less than the potential rate of evaporation, so that depletion of stored soil water is commonplace. The rate of mineralization of nitrogen (N) from organic matter and the processes of nutrient loss are closely related to the availability of soil water. Results from Kenya indicate the rapid changes in nitrate availability following rain.<br>Nutrient supply has a large effect on the quantity of radiation intercepted and hence, biomass production. There is considerable scope for encouraging canopy expansion to conserve water by reducing evaporation from the soil surface in environments where it is frequently rewetted, and where the unsaturated hydraulic conductivity of the soil is sufficient to supply water at the energy limited rate (e.g. northern Syria). In regions with high evaporative demand and coarse-textured soils (e.g. Niger), transpiration may be increased by management techniques that reduce drainage.<br>Increases in atmospheric [CO2] are likely to have only a small impact on crop yields when allowance is made for the interacting effects of temperature, and water and nutrient supply. <br>  相似文献   

3.
Research in river-floodplain systems has emphasized the importance of nutrient delivery by floodwaters, but the mechanisms by which floods make nutrients available are rarely evaluated. Using a laboratory re-wetting experiment, we evaluated the alternative hypotheses that increased nutrient concentrations in riparian groundwater during flash floods are due to (H1) elevated nutrient concentrations in surface floodwaters entering the riparian zone or (H2) re-mobilization of nutrients from riparian soils. We sampled soils from the riparian zone of a 400m reach of Sycamore Creek, AZ. Two sub-samples from each soil were re-wetted with a solution that mimicked the chemistry of floodwaters, with one sub-sample simultaneously treated with a biocide. We also measured structural characteristics of soils (texture, organic matter, moisture, and extractable nutrients) to investigate relationships between these characteristics and response to re-wetting. Riparian soils exhibited considerable variation in physical and chemical structure. Soil organic matter, moisture, and texture co-varied among samples. Re-wetting increased concentrations of nitrate and ammonium, and decreased SRP, relative to initial concentrations. Live soils were significantly lower in NO3-and SRP than biocide-treated samples. Extractable DIN pools were the best predictors of mobilization, and soil organic matter was strongly correlated with nitrate losses, probably via its relationship with microbial uptake. Nutrient mobilization and processing also varied considerably with depth, lateral position, and among plots. We estimate that 70–80% of N in riparian groundwater during flash floods is re-mobilized from riparian soils, but are unable to reject the hypothesis that flood inputs may be important sources of nutrients to riparian soils over longer time scales.  相似文献   

4.
Traditionally, crop production in sub-Saharan Africa (SSA) depends primarily on mining soil nutrients. Integrated Soil Fertility Management (ISFM) is an approach for intensifying agriculture in SSA that aims at maximizing the agronomic efficiency (AE) of applied nutrient inputs. ISFM contains the following essential components: proper fertilizer management, use of improved varieties, the combined application of organic inputs and fertilizer, and adaptation of input application rates to within-farm soil fertility gradients where these are important. This paper evaluates, through meta-analysis, the impact of these components on the AE of fertilizer N (N-AE), defined as extra grain yield per kg fertilizer N applied, in maize-based systems in SSA. Since N-AE is low for excessive fertilizer N application rates or when fertilizer is applied on fertile, unresponsive soil, as was confirmed by scatter plots against control yields and fertilizer N application rates, such values were removed from the database in order to focus on and elucidate the more variable and complex responses under less than ideal conditions typical for SSA. Compared with local varieties, the use of hybrid maize varieties significantly increased N-AE values (17 and 26 kg (kg N)?1, respectively) with no differences observed between local and improved, open-pollinated varieties. Mixing fertilizer with manure or compost resulted in the highest N-AE values [36 kg (kg N)?1] while organic inputs of medium quality also showed significantly higher N-AE values compared with the sole fertilizer treatment but only at low organic input application rates (40 and 23 kg (kg N)?1, respectively). High quality organic inputs (Class I) and those with a high C-to-N ratio (Class III) or high lignin content (Class IV) did not affect N-AE values in comparison with the sole fertilizer treatment. Application of N fertilizer on infields resulted in significantly higher N-AE values [31 kg (kg N)?1] compared with the outfields [17 kg (kg N)?1]. The obtained information indicates that N-AE is amenable to improved management practices and that the various components embedded in the ISFM definition result in improvements in N-AE.  相似文献   

5.
The assessment of the soil resource of any region has two parts, namely, an inventory of the kinds of soil and their distribution, and knowledge of the way each kind can be used and its performance under a range of circumstances. Soil varies substantially and intricately over short distances in most parts of the world. Inventory by field survey and air-photo interpretation must be done at a local scale. Inventories may be combined so that an individual nation state or region of similar size can know what kinds of soil it has, how much and where they are, how much each can produce, how to manage each in perpetuity, and the risks of degradation in use. Local classifications, with classes defined simply and identifiably on aerial photographs, will serve for mapping, and in combination with classical statistics can provide sound estimates from stratified sampling and agronomic experimentation.<br>Sound assessment should also be at this local scale initially. This should combine fundamental understanding of the soil''s behaviour, strategic agronomic research on regional stations, and on-farm trials. The last are crucial for estimating productivity of the soil in practice.<br>Data from all sources can be stored, sorted and displayed by geographic information systems that now have abundant capacity. They should be indexed by soil class and other attributes, with clear distinction being made between assessments of productive potential and basic data. They should be publicly accessible, to ensure that data are readily available and never lost.<br>Estimates of the soil resource and its productivity for large regions, nation states, and the world can be compiled from local surveys by sampling through a ''bottom-up'' procedure. <br>  相似文献   

6.
Landslides are a frequent disturbance in montane tropical rainforests that result in heterogeneous environments for plant and soil development. Natural inputs of organic matter and associated nutrients contribute to soil fertility patchiness within landslides. To test the importance of organic matter and nutrient addition to landslide soil fertility and plant growth, we mixed three types of organic matter substrates that are common to landslides (Cecropia leaves, Cyathea fronds, and forest soil) and commercial fertilizer into recently eroded soil on five landslides in Puerto Rico. In addition, we sowed seeds of two common landslide colonists (Paspalum and Phytolacca) into the soil treatment plots in order to test treatment effects on seed germination and seedling growth. Soils, seed germination, and seedling growth were monitored for one year and the field experiment was replicated in a one-year screen-house experiment. Despite highly variable initial landslide conditions, responses to soil treatments were similar across all five landslides. The forest soil addition increased total soil nitrogen and soil organic matter on landslides within 60 days, whereas Cecropia leaves provided increased soil organic matter only after 210 days. Commercial fertilizer increased plant-available soil nitrogen and phosphorus within 60 days, and also increased seed germination of Paspalum seeds when compared to soils treated with Cecropia leaves. Despite these positive effects of treatments on soils and germination, there were no treatment effects on seedling growth in the field, perhaps due to leaching or other losses of soil nutrients evident in the lack of significant treatment differences in soil resources at 370 days. In the screen-house, forest soil and commercial fertilizer treatments significantly increased soil fertility and seedling growth of both Paspalum and Phytolacca compared to control treatments. These different responses to three common types of organic matter inputs create patchy soil conditions with important implications for plant colonization and landslide succession.  相似文献   

7.
Trees have a different impact on soil properties than annual crops, because of their longer residence time, larger biomass accumulation, and longer-lasting, more extensive root systems. In natural forests nutrients are efficiently cycled with very small inputs and outputs from the system. In most agricultural systems the opposite happens. Agroforestry encompasses the continuum between these extremes, and emerging hard data is showing that successful agroforestry systems increase nutrient inputs, enhance internal flows, decrease nutrient losses and provide environmental benefits: when the competition for growth resources between the tree and the crop component is well managed. The three main determinants for overcoming rural poverty in Africa are (i) reversing soil fertility depletion, (ii) intensifying and diversifying land use with high-value products, and (iii) providing an enabling policy environment for the smallholder farming sector. Agroforestry practices can improve food production in a sustainable way through their contribution to soil fertility replenishment. The use of organic inputs as a source of biologically-fixed nitrogen, together with deep nitrate that is captured by trees, plays a major role in nitrogen replenishment. The combination of commercial phosphorus fertilizers with available organic resources may be the key to increasing and sustaining phosphorus capital. High-value trees, ''Cinderella'' species, can fit in specific niches on farms, thereby making the system ecologically stable and more rewarding economically, in addition to diversifying and increasing rural incomes and improving food security. In the most heavily populated areas of East Africa, where farm size is extremely small, the number of trees on farms is increasing as farmers seek to reduce labour demands, compatible with the drift of some members of the family into the towns to earn off-farm income. Contrary to the concept that population pressure promotes deforestation, there is evidence that demonstrates that there are conditions under which increasing tree planting is occurring on farms in the tropics through successful agroforestry as human population density increases. <br>  相似文献   

8.
The dynamics of the main nutrient fluxes of the biological cycle were quantified in a clonal Eucalyptus plantation throughout the whole planted crop rotation: current annual requirements of nutrients, uptake from the soil, internal translocations within trees, return to soil (litterfall and crown leaching) and decomposition in the forest floor. As reported for other species, two growth periods were identified in these short-rotation plantations: (1) a juvenile phase up to canopy closure, during which the uptake of nutrients from the soil reserves supplied most of the current requirements; and (2) a second phase up to harvest, characterized by intense nutrient recycling processes. Internal translocation within trees supplied about 30 % of the annual requirements of N and P from 2 years of age onwards, and about 50 % of the K requirement. The mineralization of large amounts of organic matter returned to the soil with litterfall during stand development represented a key process providing nutrients to the stand at the end of the rotation. The importance of the recycling processes was clearly shown by the small amounts of nutrients permanently immobilized in the ligneous components of trees, compared with the total requirements accumulated over the stand rotation which were two to four times higher. Small pools of nutrients circulating quickly in the ecosystem made it possible to produce high amounts of biomass in poor soils. The sustainability of these plantations will require fertilizer inputs that match the changes in soil fertility over successive rotations, mainly linked to the dynamics of organic matter in this tropical soil.  相似文献   

9.
Increased fertilizer input in agricultural systems during the last few decades has resulted in large yield increases, but also in environmental problems. We used data from published papers and a soil testing and fertilization project in Shaanxi province during the years 2005 to 2009 to analyze chemical fertilizer inputs and yields of wheat (Triticum aestivum L.) and maize (Zea mays L.) on the farmers'' level, and soil fertility change from the 1970s to the 2000s in the Loess Plateau in China. The results showed that in different regions of the province, chemical fertilizer NPK inputs and yields of wheat and maize increased. With regard to soil nutrient balance, N and P gradually changed from deficit to surplus levels, while K deficiency became more severe. In addition, soil organic matter, total nitrogen, alkali-hydrolysis nitrogen, available phosphorus and available potassium increased during the same period. The PFP of N, NP and NPK on wheat and maize all decreased from the 1970s to the 2000s as a whole. With the increase in N fertilizer inputs, both soil total nitrogen and alkali-hydrolysis nitrogen increased; P fertilizer increased soil available phosphorus and K fertilizer increased soil available potassium. At the same time, soil organic matter, total nitrogen, alkali-hydrolysis nitrogen, available phosphorus and available potassium all had positive impacts on crop yields. In order to promote food safety and environmental protection, fertilizer requirements should be assessed at the farmers'' level. In many cases, farmers should be encouraged to reduce nitrogen and phosphate fertilizer inputs significantly, but increase potassium fertilizer and organic manure on cereal crops as a whole.  相似文献   

10.
The major agricultural intensifications in the developed world over the last half century have produced a range of important environmental problems. These include pollution, damage to wildlife and landscape and other issues, both on- and off-site. These are largely being controlled by scientific investigation and Government regulation. As developing countries increase agricultural production over the next 30 years, this may also cause even more serious environmental damage.<br>The paper distinguishes between production-related on-site damage, and off-site and more extensive effects. Both may involve soil and water effects, such as soil erosion, salinization, siltation, eutrophication and loss of water quality. The use of more agrochemicals can damage water quality, health, wildlife and biodiversity. Loss of habitat from the extension of farming is particularly damaging to biodiversity. A developing off-site problem is the production of greenhouse gases by farming systems, including the conversion of forests to farmland. In the future the introduction of genetically engineered species of plants, animals or microbes will need secure control.<br>Work, probably on a catchment basis, is necessary to understand and control these problems. The three main requirements are much better environmental information from the developing world; the selection of environmental indicators to be monitored; and the support of local farmers in protecting the environment. There are encouraging indications of farmer concern and action over obvious on-site damage, but this may not extend to extensive off-site issues. The main danger is that developing food scarcity would cause the environmental issues to be ignored in a race for production. <br>  相似文献   

11.
Dynamics of organic matter in soils   总被引:11,自引:0,他引:11  
E. A. Paul 《Plant and Soil》1984,76(1-3):275-285
Summary Dynamics of C, N, S, and to some extent P are expressed by a knowledge of the size and turnover rates of plant constituents such as soluble C and N components, cellulose and hemicellulose, and lignin. Soil organic matter constituents include: the microbial biomass as determined chemically or microscopically, non-biomass active components determined by isotopic dilution, stabilized N constituents for which good techniques are not yet available, and resistant or old C and associated N determined by carbon dating. The processes involved in the nutrient transformations and transfers are reasonably well understood. The control mechanisms require further elucidation to be able to extrapolate from the laboratory to the field, and between field sites. Major control mechanisms requiring further insight include the effects of C availability on transformations of C and N. The other control for which every little is known is that of spatial compartmentalization. Compartmentalization ranges from landscape or management sequences to pedogenic layers, rhizosphere-mycorrhizal effects, clay-sesquioxide surfaces, aggregation, localized enzymes, and microbial effects such as membrane boundaries. Control mechanisms for concurrent mineralization-immobilization, the stabilization of microbial products, and the relative role of the biomass as a catalyst rather than as a source-sink for nutrients, must be understood. There is potential for combining a knowledge of microbial production and turnover with that of the roles of the soil organic active fraction as a temporary storehouse for nutrients. This, in conjunction with management techniques such as zero tillage and crop rotation, should make it possible to better utilize soil and fertilizer N, especially in areas of the world where the cost of nutrients is high relative to the value of the crop grown.Introductory lecture  相似文献   

12.
The soil microbial carbon (C), nitrogen (N) and phosphorus (P) pools were quantified in the organic horizon of soils from an arctic/alpine low-altitude heath and a high-altitude fellfield by the fumigation-extraction method before and after factorial addition of sugar, NPK fertilizer and benomyl, a fungicide. In unamended soil, microbial C, N and P made up 3.3–3.6%, 6.1–7.3% and 34.7% of the total soil C, N and P content, respectively. The inorganic extractable N pool was below 0.1% and the inorganic extractable P content slightly less than 1% of the total soil pool sizes. Benomyl addition in spring and summer did not affect microbial C or nutrient content analysed in the autumn. Sugar amendments increased microbial C by 15 and 37% in the two soils, respectively, but did not affect the microbial nutrient content, whereas inorganic N and P either declined significantly or tended to decline. The increased microbial C indicates that the microbial biomass also increased but without a proportional enhancement of N and P uptake. NPK addition did not affect the amount of microbial C but almost doubled the microbial N pool and more than doubled the P pool. A separate study has shown that CO2 evolution increased by more than 50% after sugar amendment and by about 30% after NPK and NK additions to one of the soils. Hence, the microbial biomass did not increase in response to NPK addition, but the microbes immobilized large amounts of the added nutrients and, judging by the increased CO2 evolution, their activity increased. We conclude: (1) that microbial biomass production in these soils is stimulated by labile carbon and that the microbial activity is stimulated by both labile C and by nutrients (N); (2) that the microbial biomass is a strong sink for nutrients and that the microbial community probably can withdraw substantial amounts of nutrients from the inorganic, plant-available pool, at least periodically; (3) that temporary declines in microbial populations are likely to release a flush of inorganic nutrients to the soil, particularly P of which the microbial biomass contained more than one third of the total soil pool; and (4) that the mobilization-immobilization cycles of nutrients coupled to the population dynamics of soil organisms can be a significant regulating factor for the nutrient supply to the primary producers, which are usually strongly nutrient-limited in arctic ecosystems.  相似文献   

13.
Root proliferation into the Oa and Oe soil horizons in tropical forests is often substantial and allows direct cycling of nutrients from the organic matter; this was thought to be an adaptation to the low nutrient supply in infertile soils. In this study, we show that experimentally increased litter inputs promote root proliferation into the Oi and Oe horizons in a relatively fertile soil, suggesting that it is a response to a more readily available nutrient source rather than an adaptation to nutrient shortage, and the absence of root mats on fertile tropical soils is simply a consequence of the lack of persistent organic horizons due to high decomposition rates.  相似文献   

14.
Samples of the fraction of net rainfall passing through the forest floor collected at monthly intervals in four pristine forests in Colombian Amazonia, during the period between 1995–1997 were analysed for solute concentrations to estimate the element fluxes from the forest floor into the mineral soil and root nutrient uptake from these forest floors. Results were compared with inputs by throughfall, stemflow, litterfall and fine root decay. Element concentrations were tested for their relationship with litterflow amounts, rainfall intensity and length of the antecedent dry period and differences in element fluxes between ecosystems were assessed. Concentrations of elements in litterflow followed a similar pattern as those in throughfall, which indicates that element outputs from the forest floor are strongly related to those inputs in throughfall. In the forests studied, the average concentrations of elements as K, Mg, orthoP and the pH of the litterflow decreased relative to that in throughfall in most events, while the concentration of elements such as dissolved organic carbon, H, SO4 and Si increased in litterflow from these forests. Element concentrations in litterflow showed a poor correlation with variables such as litterflow amounts, rainfall intensity and antecedent dry period, except for K which showed a significant correlation (p>0.95) with analysed variables in all forests. Outputs were significantly different between forests (p>0.95); these fluxes, which particularly concerned cations, being the largest in the flood plain, while for anions outputs increased from the flood plain to the sedimentary plain. After adding the nutrient contributed by litter decomposition and fine root decay, the net outputs of main elements from the forest floors were still smaller than inputs by net precipitation (throughfall+stemflow) indicating that the litter layers clearly acted as a sink for most nutrients. Accordingly, the element balances confirm that the forest floors acted as a sink for nutrients coming in by throughfall, stemflow, litterfall and fine root decomposition. P, Mg and N appeared to be the most limiting nutrients and the forests studied efficiently recycled these nutrients.  相似文献   

15.
The hypothesis that the importance of dissolved organic matter (DOM) as a reservoir of C, N, and P declines, relative to that of the particulate pool, with increasing nutrient inputs was tested using mesocosms exposed to a gradient of nutrient inputs in the Spanish Mediterranean. The nutrient additions included a treatment equivalent to the loading in the coastal ecosystem studied (5 mmol N m–2 d–1), and mesocosms receiving half , 2-, 4-, 8-, and 16-fold this value, as well as a mesocosm to which no nutrients were added. Nutrients were added at ratios of 20 N (as ammonium) : 7 Si : 1 P. The initial concentration of dissolved inorganic nutrients was very low (dissolved inorganic nitrogen < 0.05 M, phosphate < 0.01) and comprised, together with the particulate pool < 25% of the total N and P in the system, with the bulk N and P in the system present as DOM (> 75%). Particulate and dissolved organic matter was depleted in N (C/N ratio > 15) and, particularly, P (C/P ratio > 1000), indicative of a strongly nutrient, particularly phosphorus, deficient ecosystem. Experimental nutrient additions lead to a parabolic change in C/N and C/P ratios in the dissolved organic matter with increasing nutrient inputs, which approached the Redfield stoichiometry at nutrient inputs > 8 fold above the ambient loading. The relative size of the dissolved inorganic nutrient pools (about 20% of the N and P) did not vary, but there was a tendency towards an increase in the relative size of the particulate pool at the expense of a decrease in the relative importance of DOM as a reservoir of N, P and C, with increasing nutrient inputs. The production of nutrient-depleted organic matter at low nutrient inputs likely prevents efficient recycling, leading to the dominance of nutrients in DOM in the system.  相似文献   

16.
The Malthusian prognosis has been undermined by an exponential increase in world food supply since 1960, even in the absence of any extension of the arable area. The requisite increases in yield of the cereal staples have come partly from agronomic intensification, especially of nitrogenous fertilizer use made possible by the dwarfing of wheat and rice, in turn made feasible by herbicide development. Cereal dwarfing also contributed to a marked rise in harvest index and yield potential.<br>Although there is still scope for some further improvement in harvest index and environmental adaptation, it is not apparent how a doubling of yield potential can be achieved unless crop photosynthesis can be substantially enhanced by genetic engineering. Empirical selection for yield has not enhanced photosynthetic capacity to date, but nitrogenous and other fertilizers have done so, and there is still scope for agronomic increases in yield and for new synergisms between agronomy and plant breeding. <br>  相似文献   

17.
长期不同养分投入对土壤养分和水稻生产持续性的影响   总被引:5,自引:0,他引:5  
以中国科学院桃源农业生态试验站15a长期田间定位试验为研究对象,分析了不同养分投入对稻田土壤养分和水稻产量可持续性的影响.结果表明,化肥与系统内循环的有机物料循环的肥力效力和产量效应基本一致,有机物料循环更有利于土壤有机质和氮素的积累;在不同养分投入下,土壤耕层有机质和全氮均呈上升趋势,年均增长率分别为1.5%~5.8%和2.5%~9.4%;与试验前相比,不同养分投入耕层磷素变动幅度在-18.3%到30%之间,钾素养分有所亏缺,下降幅度在8.1%~22.6%之间;通过可持续性指数的分析得出,土壤N素养分的可持续性对化肥的依赖性较大,而P、K养分的可持续性则对有机肥的依赖性更高.稻田生态系统具有良好的自维持能力,系统内有机物循环有利于提高稻谷产量的稳定性和可持续性.  相似文献   

18.
Plant species effects on soil nutrient availability are relatively well documented, but the effects of species differences in litter chemistry on soil carbon cycling are less well understood, especially in the species-rich tropics. In many wet tropical forest ecosystems, leaching of dissolved organic matter (DOM) from the litter layer accounts for a significant proportion of litter mass loss during decomposition. Here we investigated how tree species differences in soluble dissolved organic C (DOC) and nutrients affected soil CO2 fluxes in laboratory incubations. We leached DOM from freshly fallen litter of six canopy tree species collected from a tropical rain forest in Costa Rica and measured C-mineralization. We found significant differences in litter solubility and nutrient availability. Following DOM additions to soil, rates of heterotrophic respiration varied by as much as an order of magnitude between species, and overall differences in total soil CO2 efflux varied by more than four-fold. Variation in the carbon: phosphorus ratio accounted for 51% of the variation in total CO2 flux between species. These results suggest that tropical tree species composition may influence soil C storage and mineralization via inter-specific variation in plant litter chemistry.  相似文献   

19.
Summary Routine soil-testing methods are excellent tools for monitoring soil fertility. However, if used for predicting optimal fertilizer requirements they will frequently fail. This applies especially to soils having high fertility levels needed for commercial farming with many other factors affecting plant growth. Explanatory examples are given for crop-specific nutrient requirements, for nutrient transport within the rhizosphere, for nutrient supply from subsoil and for interactions of nutrients. Soil-testing methods must become more comprehensive with regard to the number of nutrients analysed and to the rates of nutrient supply and the magnitudes of nutrient reserves.  相似文献   

20.
Summary The concept of the relative nutrient requirement (L n) that was introduced in the first paper of this series is used to analyse the effects of the dominant plant population on nutrient cycling and nutrient mineralization in wet heathland ecosystems. A distinction is made between the effect that the dominant plant species has on (1) the distribution of nutrients over the plant biomass and the soil compartment of the ecosystem and (2) the recirculation rate of nutrients. The first effect of the dominant plant species can be calculated on the basis of the /k ratio (which is the ratio of the relative mortality to the decomposition constant). The second effect can be analysed using the relative nutrient requirement (L n). The mass loss and the changes in the amounts of N and P in decomposing above-ground and below-ground litter produced by Erica tetralix and Molinia caerulea were measured over three years. The rates of mass loss from both above-ground and below-ground litter of Molinia were higher than those from Erica litter. After an initial leaching phase, litter showed either a net release or a net immobilization of nitrogen or phosphorus that depended on the initial concentrations of these nutrients. At the same sites, mineralization of nitrogen and phosphorus were measured for two years both in communities dominated by Molinia and in communities dominated by Erica. There were no clear differences in the nitrogen mineralization, but in one of the two years, phosphate mineralization in the Molinia-community was significantly higher. On the basis of the theory that was developed, mineralization rates and ratios between amounts of nutrients in plant biomass and in the soil were calculated on the basis of parameters that were independently measured. There was a reasonable agreement between predicted and measured values in the Erica-communities. In the Molinia-communities there were large differences between calculated and measured values, which was explained by the observation that the soil organic matter in these ecosystems still predominantly consisted of Erica-remains.  相似文献   

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