Mobilization of non-exchangeable K by ryegrass in five Moroccan soils with and without mica

Intensive cropping of Italian ryegrass (Lolium multiforum L.) in pots was used to assess the contribution of non-exchangeable K to plant uptake. The soils used were: two soils high in mica (illite) developed on recent alluvium plus two smectitic (beidellitic) soils and a soil of mixed mineralogy rich in mica. Four K treatments were used (0, 28.6, 143, and 286 mg kg^-1 soil) with 8 successive monthly cuttings. A response of plant K uptake to added K was observed in all soils. Both 1.0 M NH₄0Ac and 0.2 M CaCl₂ extractable K were depleted to a minimum level specific for each soil. The minima were lower in the old upland soils compared to the young alluvial soils. Uptake of K by Italian ryegrass induced K release from the non-exchangeable K to replenish the plant available pool of K ions. The release of mica interlayer K in the alluvial and in the high K smectitic soil supplied sufficient K to plants even under intensive cropping. The rate of mobilization of interlayer K was low in the smectitic soil with lower K. The lowest release rate was in the old high mica soil. Iron coatings may have inhibited mobilization of interlayer K. The rates of mobilization cannot be predicted from mineralogical and K-extraction data only. The rates of K uptake and the rates of K release by ryegrass under intensive cropping are potential values which can be used for modelling K availability to plants in the soils studied.     

A comparison of electro-ultrafiltration and quantity/intensity measurements of soil potassium with its uptake by ryegrass in Scottish soils

Summary Electro-ultrafiltration (EUF) and quantity/intensity (Q/I) parameters of soil K were compared for 14 soils from each of three soil series. The K desorbed by EUF during the first 10 min (K₁₀) was closely correlated with the equilibrium activity ratio (AR₀) for soils of the same series, but differences between series reflected the soil K-buffering capacity, indicating that K₁₀ includes loosely held exchangeable K and is not strictly an intensity measurement. EUF values were compared with conventional soil test methods for predicting K-uptake and dry-matter yield of ryegrass grown in the glasshouse. Correlation coefficients between K uptake at the first cut were 0.80 for K₁₀, 0.88 for K_a (the initially labile K derived from the Q/I curve), 0.92 for K₃₅ (desorbed by EUF in 35 min) and 0.97 for K_ex (1.0M ammonium acetate extraction).     

Phosphate adsorption and availability plant of phosphate

Summary The effects of phosphate buffer capacity on the plant-availability of labile soil phosphate, when measured as intensity (I) or quantity (Q), are described and tested using results from a greenhouse experiment on 24 Sherborne soils. In multiple regression studies, phosphate buffer capacity with I or Q measurements as independent variables accounted for up to 94% of the variance in P uptake by ryegrass, the maximum buffer capacity being generally more useful than the equilibrium buffer capacity.When the quantity of soil P is measured (Q), its availability (i.e. ease of desorption) to plant roots is inversely related to the Langmuir bonding energy parameter and the buffer capacity. When the intensity of soil P is measured (I), its availability (i.e. resistance to change) is directly related to the adsorption and buffer capacities. The levels of Q or I, therefore, which are optimal for plant uptake vary with the buffer capacity of the soil. There is little or no correlation between the adsorption capacity and the bonding energy in many soils and consequently phosphate buffer capacity is only poorly correlated with the total adsorption capacity.     

Effects of labile soil carbon on nutrient partitioning between an arctic graminoid and microbes

We measured partitioning of N and P uptake between soil microorganisms and potted Festuca vivipara in soil from a subarctic heath in response to factorial addition of three levels of labile carbon (glucose) combined with two levels of inorganic N and P. The glucose was added to either non-sterilized or sterilized (autoclaved) soils in quantities which were within the range of reported, naturally occurring amounts of C released periodically from the plant canopy. The aims were, firstly, to examine whether the glucose stimulated microbial nutrient uptake to the extent of reducing plant nutrient uptake. This is expected in nutrient-deficient soils if microbes and plants compete for the same nutrients. Secondly, we wanted to test our earlier␣interpretation that growth reduction observed in graminoids after addition of leaf extracts could be caused directly by labile carbon addition, rather than by phytotoxins in the extracts. Addition of high amounts of N did not affect the microbial N pool, whereas high amounts of added P significantly increased the microbial P pool, indicating a luxury P uptake in the microbes. Both plant N and in particular P uptake increased strongly in response to soil sterilization and to addition of extra N or P. The increased␣uptake led to enhanced plant growth when both elements were applied in high amounts, but only led to increased tissue concentrations without growth responses when the nutrients were added separately. Glucose had strong and contrasting effects on plant and microbial N and P uptake. Microbial N and P uptake increased, soil inorganic N and P concentrations were reduced and plant N and P uptake declined when glucose was added. The responses were dose-dependent within the range of 0–450 μg C g⁻¹ soil added to the non-sterilized soil. The opposite responses of plants and microbes showed that plant acquisition of limiting nutrients is dependent on release of nutrients from the soil microbes, which is under strong regulation by the availability and microbial uptake of labile C. Hence, we conclude, firstly, that the microbial populations can compete efficiently with plants for nutrients to an extent of affecting plant growth when the microbial access to labile carbon is high in nutrient deficient soils. We also conclude that reduced growth of plants after addition of leaf extracts to soil can be caused by carbon-induced shifts in nutrient partitioning between plants and microbes, and not necessarily by phytotoxins added with the extracts as suggested by some experiments. Received: 15 February 1997 / Accepted: 12 July 1997     

Phosphorus regulation of nitrogen fixation in a traditional Mexican agroecosystem

Although nitrogen is considered to be the nutrient that most commonly limits production of natural and managed terrestrial ecosystems, I propose that phosphorus may regulate productivity in many continuously cultivated agroecosystems that do not receive applications of synthetic fertilizers. One way P may limit agroecosystem productivity is by controlling nitrogen fixation of legume crops, thus affecting nitrogen availability in the overall agroecosystem. I tested this hypothesis in two studies by examining the effect of phosphorus nutrition on nitrogen fixation of alfalfa in traditional Mexican agroecosystems. All farms used in the research relied on alfalfa as the primary nitrogen source for maize cultivation and other crops, and had minimal or no reliance on synthetic fertilizers.In one study, I used the natural abundance of¹⁵N to estimate nitrogen fixation in five alfalfa plots with soils representing a wide range of P fertility. I found a correlation of r = 0.85 between foliage P concentrations and nitrogen fixation in the alfalfa plots. Mean nitrogen fixation in alfalfa plots ranged between 232–555 kg ha^–1 yr^–1 as estimated by the¹⁵N-natural abundance method.In a second study, I sampled soils from alfalfa plots on traditional farms located in 5 different physiographic regions of Mexico. Half of each soil sample was augmented with phosphorus in a greenhouse experiment. I grew alfalfa on the fertilized and unfertilized soils from each site and then determined nitrogenase activity (acetylene reduction) of the Rhizobium on the plant roots. Nitrogenase activity increased in the alfalfa grown on all soils with added phosphorus, with two of the five differences being statistically significant at P < 0.01, 0 and one at P < 0.05. Foliage P concentrations and nitrogenase activity were 0 positively correlated (r = 0.81,P < 0.01).0     

The quantity-intensity relations of potassium in soils from plots having nine fixed crop rotations for six years

Summary Soil samples collected 6 years after raising of various cereals, pulses, oil seed and tuber crops in nine fixed rotations were used to study the quantity-intensity relations of potassium. Potassium activity ratio, where the soil neither gains nor looses K, was correlated in a highly significant manner (P = 0.01) with the total amount of K fertilizer applied during 6 years. The K buffering capacity, the slope of the Q/I curve, when the soil neither gains nor looses K, was positively correlated (P = 0.05) with K saturation of the total and inorganic cation exchange capacities to a similar extent. Superimposing Q/I curves showed no appreciable difference between samples from different treatments. Desorption of potassium with increasing soil∶solution (0.01M CaCl₂) ratio followed a Langmuir type of equation and supported the conclusions drawn from quantity-intensity curves.     

Iron Reduction and Soil Phosphorus Solubilization in Humid Tropical Forests Soils: The Roles of Labile Carbon Pools and an Electron Shuttle Compound

The affinity of iron oxides and hydroxides for phosphorus is thought to contribute to phosphorus limitation to net primary productivity in humid tropical forests on acidic, highly weathered soils. Perennially warm, humid conditions and high biological activity in these soils can result in fluctuating redox potential that in turn leads to considerable iron reduction in the presence of labile carbon and humic substances. We investigated the effects of reducing conditions in combination with the addition of labile carbon substrates (glucose and acetate) and an electron shuttle compound on iron reduction and phosphorus release in a humid tropical forest soil. Glucose or acetate was added to soils as a single dose at the beginning of the experiment, and as pulsed inputs over time, which more closely mimics patterns in labile carbon availability. Iron reduction and phosphorus mobilization were weakly stimulated by a single low level addition of carbon, and the addition of the electron shuttle compound with or without added carbon. Pulsed labile carbon additions produced a significant increase in soil pH, soluble iron, and phosphorus concentrations. Pulsed labile carbon inputs also promoted the precipitation of ferrous hydroxide complexes which could increase the capacity for P sorption, although our results suggest that rates of P solubilization exceeded re-adsorption. Plant and microbial P demand are also likely to serve as an important sinks for released P, limiting the role of P re-adsorption. Our results suggest that reducing conditions coupled with periodic carbon inputs can stimulate iron reduction and a corresponding increase in soil phosphorus mobilization, which may provide a source of phosphorus to plants and microorganisms previously undocumented in these ecosystems.     

Wheat, canola and grain legume access to soil phosphorus fractions differs in soils with contrasting phosphorus dynamics

Despite the high phosphorus (P) mobilizing capacity of many legumes, recent studies have found that, at least in calcareous soils, wheat is also able to access insoluble P fractions through yet unknown mechanism(s). We hypothesized that insoluble P fractions may be more available to non-legume plants in alkaline soils due to increased dissolution of the dominant calcium(Ca)-P pool into depleted labile P pools, whereas non-legumes may have limited access to insoluble P fractions in iron(Fe)- and aluminium(Al)-P dominated acid soils. Four crop species (faba bean, chickpea, wheat and canola) were grown on two acid and one alkaline soil under glasshouse conditions to examine rhizosphere processes and soil P fractions accessed. While all species generally depleted the H₂O-soluble inorganic P (water Pi) pool in all soils, there was no net depletion of the labile NaHCO₃-extractable inorganic P fraction (NaHCO₃ Pi) by any species in any soil. The NaOH-extractable P fraction (NaOH Pi) in the alkaline soil was the only non-labile Pi fraction depleted by all crops (particularly canola), possibly due to increases in rhizosphere pH. Chickpea mobilized the insoluble HCl Pi and residual P fractions; however, rhizosphere pH and carboxylate exudation could not fully explain all of the observed Pi depletion in each soil. All organic P fractions appeared highly recalcitrant, with the exception of some depletion of the NaHCO₃ Po fraction by faba bean in the acid soils. Chickpea and faba bean did not show a higher capacity than wheat or canola to mobilize insoluble P pools across all soil types, and the availability of various P fractions to legume and non-legume crops differed in soils with contrasting P dynamics.     

Mineralization of15N-labelled legume residues in soils with different nitrogen contents and its uptake by Rhodes grass

Summary Soil was collected from pots that had grown 1,3 or 6 soybean (Glycine max) or Siratro (Macroptillium atropurpureum) crops that had received organic residue returns from each crop.¹⁵N-labelled residues were added to half the pots in the experiment and the other half left unamended. Half of each group was then sown to Rhodes grass (Chloris gayana) which was grown, under glasshouse conditions, for 12 weeks.Ten grams of organic matter residues were added to each pot (1.5 kg soil) and the pots subjected to two wetting and drying cycles. At the end of the second wet cycle, soil mineral N values ranged from 6 to 64 ppm in unamended soils and from 19 to 177 ppm in amended soils. These levels generally declined over a 12 week period both in the presence and absence of sown grass.Nitrogen uptake by the grass increased with the number of previous cycles and was higher in Siratro than soybean soils. Recovery of¹⁵N by plant growth from the incorporated soybean residues was little effected by previous crop history and averaged 15.4%. On the other hand, Siratro recoveries were 13.7, 42.4 and 55.5% from soils that had grown 1, 3 and 6 previous Siratro crops, respectively.The addition of organic residues stimulated the release of native organic N (positive priming effect) on all soils.These results show that the turnover rate of nitrogen from organic residues can be high and the net result of these additions depends on the nature of the organic residues and the soil system to which they are added. These data emphasise the need to consider the rate of nutrient turnover from organic sources rather than concentrate on the nature and size of the resident nutrient pools.     

Microbial Metabolism and Dynamic Changes in the Electrical Conductivity of Soil Solutions: a Method for Detecting Extraterrestrial Life

The addition of 0.5% glucose solutions to 12 different air-dried soils always resulted in increased electrical conductivity and water-soluble Ca and Mg in the soil solutions. The kinetics and magnitude of these changes for at least two and usually all three of these parameters over a 14-day period were clearly distinguishable from the changes in heat-sterilized controls or unsterilized controls without added glucose. In general, maximal values were achieved more rapidly under aerobic than anaerobic incubation. Some soils (less than half) also showed significant increases in water-soluble Na or K when compared with the controls. The 12 different soils studied represented four general soil groups: I, leached acid upland soils; II, saline alkaline soils; III, nonsaline neutral soils; and IV, high organic soils. Viable counts ranged from 10(4) to 10(7) per cm(3) of air-dried soil. Glucose metabolism by the indigenous soil microbiota was always accompanied by a significant decrease in the pH of soil solutions, but not necessarily by an increase in the viable count. The feasibility of using electrical conductivity and water-soluble Ca and Mg measurements to detect metabolic activity, either alone or in conjunction with other life detection techniques, is discussed.     

Phosphate potential and phosphate capacity of soils

Summary The relationship between the phosphate potential (I) and the amount of phosphate (Q), added to the soil has been examined by equilibrating soil samples with 0.001M or 0.01M CaCl₂ solutions containing various amounts of phosphate. For one neutral and two alkaline soils the Q/I relationship depends on the CaCl₂ concentration and the pH in such a way that the apparent values of I decrease when the CaCl₂ concentration increases from 0.001 M to 0.01M. The difference between the two values increases when the pH increases. When correction is made for the formation of the soluble calcium phosphate complex, CaHPO₄, the Q/I relationship becomes independent of the CaCl₂ concentration. The initial phosphate potential (I₀) determined by interpolation, is also found to be independent of the CaCl₂ concentration. The necessary amount of phosphate to be added or removed per gram of soil in order to obtain a certain alteration of the phosphate potential is designated the differential phosphate potential buffering capacity, DPBC. For ten soils DPBC-values are determined on the basis of the Q/I relationships, (ΔQ/ΔI)_Io, and found to be independent of the CaCl₂ concentration. The content of colloids and of inorganic phosphate accounts for a significant part of the variation in the DPBC for different soils. The importance of the DPBC for characterization of the phosphate status of soils in respect to phosphate supply to plants is briefly discussed. The author is indebted to professor, Dr. H. C. Aslyng, head of the department for his suggestions and helpful criticism during the progress of this work.     

On the tropical soils; The influence of organic matter (OM) on phosphate bioavailability

Application of organic manure (OM) and crop residues in agricultural soils can potentially influence positively or negatively the availability of soil phosphorus (P) through soil mineralization, sorption, or desorption of soil-bound P. Traditionally, the addition of OM can reduce the capacity of the soil colloids to adsorb P, thus increasing the release of P in soil solution, but also added OM can increase the adsorption site and increase the fixation or sorption of P to soil colloids, thus reducing the availability of P in soil solution and loss to the environment. The highly weathered tropical soils (HWTS) are susceptible to P insufficiency because HWTS have high P adsorption and fixation; this is mainly due to high concentration of P adsorbent. The main P adsorbents in HWTS include Al, Fe, Ca, and clay minerals, which are principally the same binding or adsorbent for OM compounds, but in excess, are toxic (Al and Fe) to crops. Thus, the presence of OM in HWTS can compromise the adsorption and availability of P in agricultural soils following phosphatic fertilizer applications. In this study, the influence of OM on P adsorption and availability was characterized to have a clear understanding of how OM influences P availability in agricultural soils, especially in highly weathered tropical soil. It is clearly outlined that the application of OM and crop residues can positively or negatively influence the availability of P in agricultural soils for plant uptake and dictate the P that is available for loss to the environment. Thus, the addition of organic matter as a strategy to increase P bioavailability for plant uptake must be treated with care because their contribution is not strait forward to be positive in many agricultural soils.     

Effects of phosphate buffer capacity of soil on the phosphate requirements of plants

Summary Plant-uptake and yield data for ryegrass in a greenhouse experiment are used to estimate the theoretical fertilizer phosphate requirement (Pf) of 24 Sherborne soils. Pf is shown to be a function of three parameters: (i) quantity of P required by the plant (Pr) for optimum yield; (ii) quantity of soil P (Qr) required to maintain a non-limiting soil solution concentration (Ir); (iii) quantity of labile soil P (Q). Because of its large effect on Qr and Ir, the phosphate buffer capacity has an important effect on Pf. However Pf cannot be directly related to phosphate buffer capacity if Q is ignored. On soils of similar Q, increasing buffer capacity will always have a positive effect on Pf, but on soils of the same I, it may have a positive or negative effect on Pf. Consequently, Pf can only be simply, but inversely, related to Q or I on a group of soils of similar phosphate buffer capacity. re]19750513     

Changes in soil phosphorus fractions following sole cropped and intercropped maize and faba bean grown on calcareous soil

Aims

This study aimed to investigate the effects of coexistence with faba bean, a phosphorus (P)-efficient crop, on soil-accumulated P use by a maize/faba bean intercropping system on dynamic changes in soil P pool.

Methods

Maize and faba bean were grown in P-accumulated soil as either sole cropping or intercropping. After one year (Stage I) or four years (Stage II) of no P application, soil samples were collected respectively and analyzed for soil P pools using sequential fractionation. Aboveground biomass and P content were annually measured from 2013 to 2016 to assess the annual P balance.

Results

The intercropped maize/faba bean system showed a P-uptake advantage, with a Land Equivalent Ratio (LER) ranging from 1.2 to 1.5. The average shoot P content over the four years in intercropped maize and faba bean was significantly greater than that of the corresponding sole crops by 29% and 30%, respectively. Over the three-year P depletion period, the three cropping systems primarily depleted the 1 M HCl-P_i fraction, followed by sole maize, which depleted the NaOH-P_i and concentrated HCl-P_o fractions. Sole faba bean depleted the alkali-soluble P_o fraction (extracted by NaHCO₃ and NaOH), and the intercropped maize/faba bean system depleted the conc. HCl-P_o fraction, which was similar to the effect of sole maize.

Conclusions

Both sole crops and intercrops mainly depleted 1 M HCl-P_i, but differed in P_o depletion. Sole maize and maize/faba bean intercropping depleted the sparingly labile P_o fraction, while sole faba bean depleted the labile and moderately labile P_o fractions.

     

Density‐dependent parasitism in biological control of soil‐borne insects,nematodes, fungi and bacteria

Temporal density‐dependent parasitism appears to explain the development of some pest‐ and pathogen‐suppressive soils. In many examples, an enrichment of hosts (soil‐borne pests or pathogens) precedes and supports a build up of beneficial parasites in perennial crops or in monocultures, and the population dynamics of hosts and parasites may be described in epidemiological terms. Although the examples support the concept of a balance of nature based on density‐dependent regulation, we lack detailed understanding of the processes that drive these beneficial epidemics. In addition, the epidemics develop slowly and often do not provide the control expected by farmers. Current research, therefore, emphasizes inundative release of beneficial agents. Nevertheless, we should study epidemics in soil in order to learn how they might be enhanced; to learn how better to utilize inoculum that is inundatively added to soil; and to contribute to the general discussion of population biology and regulation.     

Phosphorus management for perennial crops in central Amazonian upland soils

The present contribution discusses the soil P status of central Amazonian upland soils, the effects of tree crops on soil P availability and the factors controlling soil P cycling in land use systems with tree crops. Soil fertility management has to target the prevalent P deficiency by adequate P fertilization, especially in southern and northern municipalities of central Amazônia where the largest areas with severe P deficiency are found. P fixation to clay minerals is not a major obstacle for P management in the highly weathered upland soils of the central Amazon due to their low Al- and Fe-oxide contents. Low total soil P amounts are mainly responsible for low P availability. Tree crops are found to be especially suitable for land use under low-P-input conditions. Their large P return to soil by litterfall and pruning improves soil P availability. Additionally, litter quality affects P release and soil P availability. Both aspects, quantity and quality effects, are strongly dependent on tree species. Phosphorus sorption does not seem to be reduced by different litter types confirming earlier results that P fixation is not a major problem in central Amazonian upland soils. In conclusion, biological approaches are more important than physical approaches to improve soil P availability in central Amazonian Oxisols. With large P cycling through soil microbial biomass and between plant and soil, a higher availability of added P can be maintained and P applications only need to replenish P exports by harvest. Low P additions will improve productivity also for long-term uptake by trees. This is of high importance in regions with poor infrastructure and the lack of financial resources.     

Build up and depletion of soil phosphorus and potassium and their uptake by rice and wheat in a long-term field experiment

Summary In a field experiment initiated at the Central Soil Salinity Research Institute, Karnal in 1974 involving rice wheat cropping sequence and NPK fertilizer use on sodic soil (pH 9.2, ESP 32.0), an attempt was made to evaluate the available P and K status of the soil and their uptake by the crops during 1982–83 and 83–84.Application of P to either or both the crops significantly enhanced the yields of rice and improved available P status of the soil. Wheat yields remained unaffected. Fertilizer N reduced P content in rice but increased P uptake in crops and considerably brought down available P to a level (4.5 ppm) where rice plants showed reduced tillering and phosphorus deficiency. Application of K did not affect the yield of either crop but enhanced its available status in soil and uptake by the crops. Contribution of the non-exchangeable K towards total potassium removal was about 93% in the absence of applied K which decreased to 87% with the use of K. Application of K to both crops resulted in lesser uptake from non-exchangeable form as compared to its application to either crop. Laboratory studies carried out on soils of the experimental plots showed that cumulative K release measured after five successive extractions was higher in K-treated soils as compared to untreated ones. The major difference was only in the first extraction representing the exchangeable K after which release became independent of the available K of the soil.     

Comparison of availability of phosphorus from granulated and powdered superphosphate by calculations of yield curves related to the phosphorus added and found in soil and plant tests

Summary The efficiency of superphosphate in granular and powder form was compared in four typical Israeli agricultural soils in a greenhouse investigation. Under greenhouse conditions no advantage was found for the granular form either in the first crop (clover) or in the second following crop (corn). The efficiency of superphosphate forms was evaluated from Mitscherlich yield curves by comparing the constants which determine the slopes of the curves (c).Soil samples were taken from the pots and soluble phosphorus in three different extractions was related to the relative yields obtained. The NH₄F extract gave a fairly good correlation for both crops tested and all experimental soils included. The NaHCO₃ extract gave a good correlation for the clover crop.Phosphorus was determined in the clover plants and the amount of phosphorus extracted by plants was related to soil tests. Generally, very good correlations were obtained if they were calculated individually for each soil.Laboratory experiments showed that the added water-soluble phosphorus is relatively quickly fixed into insoluble forms (in water and NaHCO₃ solution) in three out of four soils. In the fourth, a coarse-textured soil, the fixation power is relatively low.     

易分解有机碳对不同恢复年限森林土壤激发效应的影响

土壤有机碳库作为陆地生态系统最大的碳库,其微小的改变都将引起大气CO_2浓度的急剧改变。易分解有机碳的输入可以通过正/负激发效应加快/减缓土壤有机碳(SOC)的矿化,并最终影响土壤碳平衡。以长汀县不同恢复年限森林(裸地、5年、15年、30年马尾松林以及天然林)土壤为研究对象,通过室内培养向土壤中添加~(13)C标记葡萄糖研究易分解有机碳输入对不同恢复阶段森林土壤激发效应的影响。研究结果表明,易分解有机碳输入引起的土壤激发效应的方向和强度因不同恢复阶段而异。易分解有机碳输入的初期对各恢复阶段森林土壤均产生正的激发效应,然而随着时间的推移,15年、30年马尾松林以及天然林相继出现负的激发效应。从整个培养期(59 d)来看,易分解有机碳的输入促进了裸地与5年生马尾松林土壤有机碳的矿化,有机碳的矿化量分别提高了131%±27%与25%±5%;但是减缓了15年生马尾松林土壤有机碳的矿化,使其矿化量减少了10%±1%;然而,易分解有机碳输入对30年生马尾松林及天然林土壤有机碳的矿化则无明显影响。土壤累积激发碳量与葡萄糖添加前后土壤氮素的改变百分比呈显著正相关关系(R~2=0.44,P0.05),表明易分解有机碳输入诱导的土壤激发效应受土壤氮素可利用性的调控,土壤微生物需要通过分解原有土壤有机碳释放的氮素来满足自身的需求。     

Effects of vesicular-arbuscular mycorrhiza on the size of the labile pool of soil phosphate

Summary Inoculation of lettuce, onion and clover with VA mycorrhizal fungus (Glomus mosseae) increased plant yields and phosphate uptake in three soils that had been depleted in phosphate. From two soils in which the labile pool of phosphate had been labelled with³²P, the specific activity of plant phosphate was the same whether the plants were mycorrhizal or non-mycorrhizal. In a third soil (Sonning) the specific activity was lower in lettuce and clover when the plants were mycorrhizal. When the experiment was repeated with the same soil under conditions that gave lower growth rates, the specific activity was the same in mycorrhizal and non-mycorrhizal plants. The lower specific activity in lettuce and clover in the first experiment is atributed to greater release of slowly exchanging phosphate (which is not in equilibrium with the added³²P), caused by the high uptake of phosphate by the mycorrhizal plants. When they occur, lower specific activities in mycorrhizal plants may therefore not necessarily indicate a solubilizing effect of the mycorrhiza on soil phosphate.