Soil test measures of available P (Colwell, resin and DGT) compared with plant P uptake using isotope dilution

Background and aims

Recent research has demonstrated the high accuracy of a new method for assessment of plant available P in soil called diffusive gradients in thin-films (DGT). The process of P released by additions of bicarbonate to soil samples simulating common soil P tests is yet to be assessed by the new method (DGT). The aim of this study was to identify the pools of soil P extracted by soil test methods (DGT, Colwell and resin) by comparing, in ³²P–labelled soils, the specific activity (SA) of phosphorus extracted by common soil test extracts with the SA of wheat plants grown in a range of agricultural soils from southern Australia.

Methods

Wheat (cv. Frame) was grown for 4 weeks in 14 soils that were labelled uniformly with carrier-free ³²P. The specific activity (SA) of P (MBq ³²P kg ³¹P^?1) in each soil test extract was compared to the SA of P in the wheat plants.

Results

The SA of P in plants were similar to P extracted by the Colwell extractant in only 4 of the 14 soils; while SA in plants and extractants corresponded in 10 of the soils for the resin method and in 12 of the soils for the DGT method. Phosphorus in the Colwell and resin extract solutions had significantly lower SAs compared to P in the plants for 10 and 4 of the soils, respectively, indicating greater extraction of non-labile P sources (unlabelled ³¹P). Phosphorus in the DGT extractant had significantly lower SA than the plants for 1 soil and in 1 soil the SA was higher. Overall, across all soils, 25 % of P extracted by the Colwell method was non labile compared to 9 % and 2 % for the resin and DGT methods, respectively.

Conclusion

The new DGT method for extraction of soil P has the potential to accurately predict occurrences of P deficiency because it generally extracts the same pool of labile soil P accessed by wheat plants, while methods using bicarbonate solution (e.g. Colwell, Olsen) or water (resin) at wide soil:solution ratios are more likely to measure more non-labile forms of P in soil.     

Chemical speciation of Zn in acidic soils: suitable soil extractant for assessing Zn availability to maize (Zea mays L.)

Abstract

Chemical fractions of soil Zn namely: water soluble (WS), exchangeable (EX), Pb displaceable (Pb-disp.), acid soluble (AS), Mn oxide occluded (MnOX), organically bound (OB), amorphous Fe oxide occluded (AFeOX), crystalline Fe oxide occluded (CFeOX), residual (RES) were determined in 20 surface (0–15 cm) samples of acidic soils from the provinces of Uttarakhand and Uttar Pradesh, India. The chemical fractions of soil Zn in acidic soils were found to be in the following descending order of Zn concentration: RES > CFeOX > Pb-Disp. > AFeOX > MnOX > AS > OB > EX > WS. These soil samples were also extracted by: DTPA (pH 7.3), DTPA (pH 5.3), AB-DTPA (pH 7.6), Mehlich 3 (pH 2.0), Modified Olsen, 0.01 N CaCl₂, 1 M MgCl ₂ and ion exchange resins. Chemical fractions and the soil extractable content of Zn estimated by different soil extractants were significantly correlated with some general soil properties. Maize (cv. Pragati) plants were grown in these soils for 35 days after emergence and Zn uptake by plants was compared with the amount of Zn extracted by different soil extractants and chemical fractions of Zn. Among chemical fractions of soil Zn, Pb-displaceable and acid soluble chemical fractions of soil Zn showed a significant and positive correlation with Zn uptake by maize. Path coefficient analysis also revealed that the acid soluble Zn fraction showed the highest positive and direct effect on Zn uptake (P=0.960). Among different multinutrient soil extractants evaluated for their suitability to assess Zn availability in acidic soils, DTPA (pH=5.3) was most suitable soil extractant, as the quantity of soil Zn extracted by this extractant showed a significant and positive correlation with the dry matter yield, Zn concentration and uptake by maize plants.     

Phosphorus fertilizer recovery from calcareous soils amended with humic and fulvic acids

Precipitation of Ca phosphates negatively affects recovery by plants of P fertilizer applied to calcareous soils, but organic matter slows the precipitation of poorly soluble Ca phosphates. To study the effect of high molecular weight organic compounds on the recovery of applied P, a mixture of humic and fulvic acids was applied to calcareous soils with different levels of salinity and Na saturation which were fertilized with 200 and 2000 mg P kg^–1 as NH₄H₂PO₄. Recovery was measured as the ratio of increment in Olsen P-to-applied P after 30, 60 and 150 days, and associated P forms were studied using sequential chemical fractionation and ³¹P NMR spectroscopy. Application of the humic-fulvic acid mixture (HFA) increased the amount of applied P recovered as Olsen P in all the soils except in one soil with the highest Na saturation. In soils with high Ca saturation and high Olsen P, recovery increased from < 15% in the absence of amendment to > 40% at a 5 g HFA kg^–1 amendment rate (30 days incubation and 200 mg P kg^–1 fertilizer rate). This is ascribed to inhibition of the precipitation of poorly soluble Ca phosphates, consistent with the sequential chemical extraction (reduction of the HCl extractable P) and P concentration in 0.01 M CaCl₂ (1:10 soil:solution ratio) extracts. ³¹P NMR spectra revealed that in non-amended samples, most spectral shifts were due to poorly soluble P compounds (carbonate apatite); on the other hand, at the 5 g HFA kg^–1 rate, significant amounts of amorphous Ca phosphate and dicalcium phosphate dihydrate (DCDP) were identified. The increase in the recovery of applied P due to HFA reveals a positive effect of the application of organic matter as soil amendments on the efficiency of P fertilizers and also explains that manures and other organic sources of P were more efficient increasing available P than inorganic P fertilizers in calcareous soils.     

白浆土植物系统营养物质转化机制及其有效性研究Ⅳ.环境条件对土壤磷素有效性的影响

根际试验研究表明,水分、有机质、土壤酸度是影响白浆土磷素生物有效性的重要因子．调节土壤水分含量,能增强土壤中铁、铝磷酸盐的溶解,加速磷酸根离子从根际土壤向非根际土壤扩散．增加土壤有机质含量,降低了土壤对Ｐ 素的吸附自由能（ Ｋ 值） ,提高土壤中的速效磷含量．适量施用石灰,调节白浆土酸度,由于化学溶解作用的影响,促进了土壤中铁、铝磷酸盐的溶解,增强了土壤中磷素的生物有效性     

The influence of composting and maturation processes on the heavy-metal extractability from some organic wastes

Seven mixtures from four organic residues—aerobic sewage sludge, city refuse, peat residue and grape debris—were made up to study the influence of the composting and maturation processes on the extractability of Fe, Cu, Ni, Zn, Cd, Pb, Cr and Mn by a chelating agent (diethylenetriaminepentaacetic acid, DTPA) and a neutral salt solution (0·05m CaCl₂) from the residues.Composting and maturation increased the concentration of heavy metals in the materials due to the loss of weight of the materials during these processes. The metals also became more insoluble, and extractants employed removed larger amounts of metals from the raw composts than from the mature composts. In general, CaCl₂-extractable metals did not correlate significantly with the metal content of the composts. With DTPA-extractable metals, the only ones that showed significant correlations between the quantity of metal extracted by DTPA and the metal content of the samples in nearly all the composts studied were Pb and Zn.The load of ‘zinc equivalent’ increased with the composting and maturation processes, and the Cd/Zn ratio decreased with those processes.     

Extractable sulphate and organic sulphur in soils and their availability to plants

Ten soils collected from the major arable areas in Britain were used to assess the availability of soil sulphur (S) to spring wheat in a pot experiment. Soils were extracted with various reagents and the extractable inorganic SO₄-S and total soluble S(SO₄-S plus a fraction of organic S) were determined using ion chromatography (IC) or inductively-coupled plasma atomic emission spectrometry (ICP-AES), respectively. Water, 0.016 M KH₂PO₄, 0.01 M CaCl₂ and 0.01 M Ca(H₂PO₄)₂ extracted similar amounts of SO₄-S, as measured by IC, which were consistently smaller than the total extractable S as measured by ICP-AES. The amounts of organic S extracted varied widely between different extractants, with 0.5 M NaHCO₃ (pH 8.5) giving the largest amounts and 0.01 M CaCl₂ the least. Organic S accounted for approximately 30–60% of total S extracted with 0.016 M KH₂PO₄ and the organic C:S ratios in this extract varied typically between 50 and 70. The concentrations of this S fraction decreased in all soils without added S after two months growth of spring wheat, indicating a release of organic S through mineralisation. All methods tested except 0.5 M NaHCO₃-ICP-AES produced satisfactory results in the regression with plant dry matter response and S uptake in the pot experiment. In general, 0.016 M KH₂PO₄ appeared to be the best extractant and this extraction followed by ICP-AES determination was considered to be a good method to standardise on.     

白浆土－植物系统营养物质转化机制及其有效性研究 Ⅰ．~（32）P同位素示踪法对白浆土中P肥利用率

利用３２Ｐ同位素示踪法对白浆土中Ｐ肥利用率进行了研究．结果表明,在岗地白浆土上,表层土壤表现出一定程度的供Ｐ不足现象,白浆层土壤有效Ｐ含量严重缺乏．表层土壤中当季Ｐ肥利用率的变幅范围为６．０９～１２．３５％,白浆层土壤Ｐ肥利用率为１３％左右．施用有机肥能明显提高白浆土ＯｌｓｅｎＰ的含量,加速土壤本身Ｐ的活化,各种有机物中,以猪粪对土壤潜在Ｐ的活化效果最好．将ＯｌｓｅｎＰ与Ｘ值、Ａ值比较,认为ＯｌｓｅｎＰ是评价白浆上Ｐ肥力简便易行的可靠指标．     

白浆土－植物系统营养物质转化机制及其有效性研究——Ⅰ．32P同位素示踪法对白浆土中P肥利用率

利用³²P同位素示踪法对白浆土中P肥利用率进行了研究.结果表明,在岗地白浆土上,表层土壤表现出一定程度的供P不足现象,白浆层土壤有效P含量严重缺乏.表层土壤中当季P肥利用率的变幅范围为6.09～12.35%,白浆层土壤P肥利用率为13%左右.施用有机肥能明显提高白浆土Olsen P的含量,加速土壤本身P的活化,各种有机物中,以猪粪对土壤潜在P的活化效果最好.将Olsen P与X值、A值比较,认为Olsen P是评价白浆上P肥力简便易行的可靠指标.     

白浆土 植物系统营养物质转化机制及其有效性研究Ⅳ.环境条件对土壤磷素有效性的影响

根际试验研究表明,水分、有机质、土壤酸度是影响白浆土磷素生物有效性的重要因子。调节土壤水分含量,能增强土壤中铁、铝磷酸盐的溶解,加速磷酸根离子从根际土壤向非根际土壤扩散。增加土壤有机质含量,降低了土壤对P素的吸附自由能(K值),提高土壤中的速效磷含量。适量施用石灰,调节白浆土酸度,由于化学溶解作用的影响,促进了土壤中铁、铝磷酸盐的溶解,增强了土壤中磷素的生物有效性.     

Poliovirus Adsorption by 34 Minerals and Soils

The adsorption of radiolabeled infectious poliovirus type 2 by 34 well-defined soils and mineral substrates was analyzed in a synthetic freshwater medium containing 1 mM CaCl₂ and 1.25 mM NaHCO₃ at pH 7. In a model system, adsorption of poliovirus by Ottawa sand was rapid and reached equilibrium within 1 h at 4°C. Near saturation, the adsorption could be described by the Langmuir equation; the apparent surface saturation was 2.5 × 10⁶ plaque-forming units of poliovirus per mg of Ottawa sand. At low surface coverage, adsorption was described by the Freundlich equation. The soils and minerals used ranged from acidic to basic and from high in organic content to organic free. The available negative surface charge on each substrate was measured by the adsorption of a cationic polyelectrolyte, polydiallyldimethylammonium chloride. Most of the substrates adsorbed more than 95% of the virus. In general, soils, in comparison with minerals, were weak adsorbents. Among the soils, muck and Genesee silt loam were the poorest adsorbents; among the minerals, montmorillonite, glauconite, and bituminous shale were the least effective. The most effective adsorbents were magnetite sand and hematite, which are predominantly oxides of iron. Correlation coefficients for substrate properties and virus adsorption revealed that the elemental composition of the adsorbents had little effect on poliovirus uptake. Substrate surface area and pH, by themselves, were not significantly correlated with poliovirus uptake. A strong negative correlation was found between poliovirus adsorption and both the contents of organic matter and the available negative surface charge on the substrates as determined by their capacities for adsorbing the cationic polyelectrolyte, polydiallyldimethylammonium chloride.     

川西亚高山三种森林恢复途径对土壤生物有效磷的影响

土壤生物有效磷在提高森林生产力和生物地球化学循环中起着至关重要的作用,研究不同森林恢复途径对土壤生物有效磷的影响对于退化森林的适应性恢复和可持续经营具有重要意义。选取川西亚高山不同恢复途径下形成的3种森林类型,即粗枝云杉人工林（人工种植,PF）、岷江冷杉-红桦天然次生林（自然更新,NF）和粗枝云杉阔叶混交林（人工种植后自然更新,MF）,采用基于生物有效性的土壤磷分级方法测定土壤生物有效磷（CaCl₂-P、Citrate-P、Enzyme-P和HCl-P）,探究不同森林恢复途径对土壤生物有效磷的影响。结果表明：不同森林恢复途径对土壤生物有效磷影响显著（P<0.05）,NF和MF的土壤Citrate-P和Enzyme-P显著高于PF（P<0.05）,而PF的土壤HCl-P显著高于NF（P<0.05）。自然更新是3种森林恢复途径中最能提高土壤生物有效磷的方式。3种森林恢复途径下的土壤生物有效磷组分与速效磷均呈现显著的正相关关系,且NF的土壤速效磷与生物有效磷的相关性更强（CaCl₂-P除外）。显著影响NF土壤生物有效磷的土壤理化性质有全钾、铵态氮含量和pH值,且全钾对NF的土壤生物有效磷变异的解释程度最高（r²=0.63,P=0.001）。土壤pH值、钙和可溶性有机碳含量是显著影响MF土壤生物有效磷的主要土壤理化性质（P<0.05）。对PF的土壤生物有效磷具有显著影响的土壤理化性质是土壤有机碳、铁和可溶性有机碳含量。土壤理化性质对3种恢复途径下森林土壤生物有效磷的解释率均超过了80%,森林恢复途径对土壤生物有效磷的影响与土壤理化性质有关。     

Phosphorus Limitation in Boreal Forests: Effects of Aluminum and Iron Accumulation in the Humus Layer

Plant growth in boreal forests is generally considered to be predominantly nitrogen (N) limited, but forested groundwater discharge areas may be exceptions. In this study, we conducted tests to determine whether highly productive forested groundwater discharge areas generally differ from adjacent groundwater recharge areas in terms of humus chemistry and the availability of phosphorus (P) and N to plants. We investigated six forested sites, divided into groundwater discharge and adjacent groundwater recharge areas, in northern Sweden. The humus layers of the forested groundwater discharge areas were clearly distinguished from the adjacent groundwater recharge areas by having higher acid-digestible calcium (Ca) and/or aluminium (Al) and iron (Fe) content and higher organic P and N content. Soil solution inorganic N (NH₄ ⁺ and NO₃ ⁻) and pH were higher in the groundwater discharge areas than in the groundwater recharge areas. The organic P content showed a positive linear relationship to the Al and Fe content in the humus layer, indicating that organic P is associated with Al and Fe compounds in the humus. A plant bioassay using humus substrate from one groundwater discharge area and the adjacent groundwater recharge area found that plants grown in groundwater discharge area humus (with a high P-fixation capacity) increased their biomass upon P fertilization, whereas no growth response was found for N additions. By contrast, plants grown in humus from the groundwater recharge area did not respond to added P unless N was added too. This study suggests that groundwater discharge can affect the nutrient availability of N and P both directly, via increased P fixation due to the redistribution of Al and Fe, and indirectly, via the inflow of groundwater high in Ca and alkalinity, maintaining a high pH in the humus layer that favors in situ N turnover processes. Received 2 March 2001; Accepted 9 November 2001.     

Interferences between root plaque formation and phosphorus availability for isoetids in sediments of oligotrophic lakes

Freshwater isoetids exchanges a high proportion of the photosynthetically produced oxygen over the extensive root system and, therefore, they influence the redox potential (E_h) and phosphorus (P) availability in their sediments. Because isoetids rely on the sediment for P uptake, P may be a key element in controlling the distribution of isoetids. We investigated biomass and P availability to isoetids (Littorella uniflora and Isoetes lacustris) in a transect of five stations across the littoral zone in oligotrophic Lake Kalgaard, Denmark. At the two shallowest stations (0.6 and 1.0 m depth) the redox potential in the low organic rhizosphere sediment was high (>300 mV) and low concentrations of reduced exchangeable iron (Fe) and manganese (Mn) compounds in the sediment and of precipitated Fe and Mn oxides on isoetid roots (plaques) were found. The concentration of sediment P pools was low and so was isoetid P content and isoetid biomass. At intermediate water depth (1.8 m) sediment E_h was high (300 mV) and isoetids showed low root plaque concentrations. However, higher concentration of P pools in the rhizosphere was found at 1.8 m and isoetids showed the highest P content and biomass. At deeper stations (2.8 and 4.6 m depth) E_h was low (<100 mV) in the high organic rhizosphere and high concentrations of plaques were found. The P content in the sediment was high, however, isoetids showed low biomass and low P content. We suggest that the low P content in isoetids growing on P rich organic sediments is partly due to inhibition of the P uptake because of adsorption of P to the oxidized Fe and Mn plaques. However, ratios between oxidized Fe and Fe-bound P, 150 for plaques and 40 for sediment, suggest the isoetids are able to access some of the P that is bound in the plaques. The pools of dissolved P in the porewater were 25–1100 times lower than the estimated annual P requirement for net growth of isoetids while solid fraction P pools were 20–260 times higher than the estimated annual P requirement. Clearly, the oxygen release from isoetid roots decreases the availability of P either by keeping the entire rhizosphere oxidized (low organic sediments) or by the formation of root plaques (high organic sediments).     

Test of soil extractants for their suitability in predicting Ca/Sr ratios in leaves and stems of sugar maple seedlings

Differential uptake and translocation of Ca and Sr in organisms have been reported, calling into question the use of Sr to track Ca cycling in the environment. We investigated the relationship between Ca/Sr ratios in soil extracts of various strengths (H₂O, NH₄Cl, and NH₄EDTA) and seedlings of sugar maple (Acer saccharum Marsh.) grown from natural regeneration on 37 sites. Our objectives were to determine if Ca/Sr ratios in soil extracts are correlated with those in sugar maple tissues, and what soil extractant best duplicate plant tissue Ca/Sr ratios. Leaves had higher Ca/Sr ratios than stems and the extractants did not produce equal Ca/Sr ratios: H₂O had the lowest Ca/Sr, and NH₄EDTA the highest. The relationships between soil extract Ca/Sr ratios and leaf and stem Ca/Sr ratios were significant and linear, but the slopes differed among extractants. The lowest slope (0.45) was observed for the water extract/leaves and the highest (2.15) for the NH₄EDTA extract/stem with discrimination factors ranging from 0.22 with NH₄EDTA to 1.59 for water. Leaf extracts were more strongly correlated with soil Ca/Sr than stem extracts (R ² of 0.57–0.7 vs. R ² of 0.45–0.6, respectively). These findings support the use of Ca/Sr ratios in plants to track their source of soil Ca, but they highlight the need to calibrate the relationships for the plant tissue and soil extractant used.     

Root-induced processes controlling phosphate availability in soils with contrasted P-fertilized treatments

Aims

In this study we identified the nature of the root-induced chemical processes controlling changes in phosphate (P) availability in a soil with two P loadings resulting from long-term fertilization treatments.

Methods

We used a set of mechanistic adsorption models (surface complexation and ion exchange) within the framework of the component additive approach to simulate the effect of durum wheat roots on P availability. We had to consider the influence of adsorption of other ions to ensure the goodness-of-fit of the simulations.

Results

We found that Ca²⁺ uptake, in addition to P uptake and root-induced alkalization, controlled P availability in the rhizosphere regardless of the fertilization level. The relative influence of these three processes depends primarily on the extractant used to estimate P availability. Calcium uptake was the most significant process in water extracts, whereas P uptake was the dominant root-induced chemical process in CaCl₂ extracts. Under low Ca concentrations, Ca²⁺ uptake decreased the promoting influence of Ca²⁺ adsorption on P adsorption.

Conclusions

In addition to confirming the validity of our approach to model P availability, the present investigation indicated that root-induced processes markedly affect P availability irrespective of the fertilization level.     

Soil phosphorus fractions and adsorption as affected by organic and inorganic sources

The effect of organic and inorganic sources of phosphorus (P) on soil P fractions and P adsorption was studied in a field without plant growth on a Kandiudalf in western Kenya. A high-quality organic source, Tithonia diversifolia (Hemsley) A. Gray leaves, and a low-quality source, maize (Zea mays L.) stover, were applied alone or in combination with triple superphosphate (TSP). The P rate was kept constant at 15 kg P ha^-1. Soil extractable P (resin, bicarbonate and sodium hydroxide), microbial biomass P and C and P adsorption isotherms were determined during 16 weeks after application of treatments. Application of tithonia either alone or with TSP increased resin P, bicarbonate P, microbial P, and sodium hydroxide inorganic P. Tithonia alone reduced P adsorption at 2–16 weeks. Maize stover had no effect on any of the P fractions or P adsorption. At 8 weeks, the application of tithonia reduced microbial C-to-P ratio (20) as compared to maize stover, TSP and the control (31–34). The reduction in P adsorption by tithonia was accompanied by increases in all measured P fractions, the sum of P in those fractions (resin, bicarbonate and sodium hydroxide) being larger than the P added. The reduction in P adsorption apparently resulted from competition for adsorption sites, probably by organic anions produced during decomposition of the high quality tithonia. Integration of inorganic P (TSP) with organic materials had little added benefit compared to sole application of TSP, except that combination of tithonia with TSP increased microbial biomass. The results indicate that a high quality organic input can be comparable to or more effective than inorganic P in increasing P availability in the soil.     

长期施肥下农田土壤-有机质-微生物的碳氮磷化学计量学特征

探讨外源养分的输入对土壤系统内碳、氮、磷化学计量特征的影响,对于深刻认识农田土壤有机碳(C)和养分循环及其相互作用过程具有重要意义。以26年的农田长期定位施肥试验为平台,分析长期不同施肥条件下土壤、有机态及微生物生物量碳、氮、磷含量及其化学计量学特征,并根据内稳性模型y=c x~(1/H)计算其化学计量内稳性指数H。结果表明:与长期撂荒处理(CK_0)相比,种植作物条件下26年化肥配施有机肥处理(MNPK和1.5MNPK)显著降低微生物生物量氮含量,但显著提高了微生物生物量磷的含量。相对于撂荒处理,即使长期配施化肥磷处理(NP、PK、NPK),其土壤有机磷降低显著。对于C∶N比而言,化肥配施有机物料处理(秸秆或有机肥)的土壤C∶N比、有机质C∶N及微生物生物量C∶N比均显著低于化肥处理(N、NP、PK和NPK)。对于C∶P比而言,相对于撂荒处理,26年施用磷肥(化肥磷或有机磷)显著降低了土壤C∶P比和微生物生物量C∶P比,而CK和偏施化肥处理(N、NP和PK)显著降低了土壤有机质C∶P比。对于土壤N∶P比而言,撂荒处理土壤N∶P比显著高于其他处理,而撂荒处理土壤有机质N∶P比显著高于CK和化肥处理,表明不施肥或化肥条件下作物种植加剧了土壤有机质中氮素的消耗。微生物生物量C∶N、C∶P、N∶P比的内稳性指数H分别为0.24、0.75、0.64,不具有内稳性特征。微生物生物量C∶N、C∶P、N∶P比分别与土壤C∶N、C∶P、N∶P比呈显著正相关关系,但与土壤有机质碳氮磷化学计量比之间无显著相关性。表明土壤碳、氮、磷元素的改变会直接导致微生物生物量碳、氮、磷化学计量比的改变,但微生物生物量碳氮磷化学计量比对土壤有机质碳氮磷化学计量比无显著影响,土壤有机质的碳氮磷计量比可能更多是受到作物和施肥等养分管理措施的影响。     

长期定位施肥与地膜覆盖对土壤肥力和生物学性质的影响

采集沈阳农业大学棕壤定位实验站(1987年设置)的土样,测定土壤pH、有机碳、全氮、碱解氮、速效磷、速效钾、微生物生物量碳、氮和BIOLOG碳源利用,结合地上部分生物量,系统分析了长期施肥与地膜覆盖对土壤肥力指标和微生物学性质的影响.结果表明,传统栽培条件下,土壤微生物群落平均吸光度(AWCD)与土壤有机碳含量、速效磷和有效钾显著相关(p<0 01),表明施肥通过影响有机碳和速效磷、钾含量影响微生物功能.在覆膜栽培条件下,AWCD与土壤pH和土壤碳氮比显著相关(p<0.01),表明覆膜通过影响土壤pH和土壤碳氮比影响微生物功能.覆膜引起玉米生育期的变化,影响有效碳的投入,从而直接影响土壤微生物功能.与相应的传统栽培相比,覆膜栽培后土壤pH的变化对微生物群落结构有一致影响.     

定位施肥对紫色菜园土磷素状况的影响

基于紫色菜园土壤莴笋-白菜轮作3a的12季连续定位施肥试验,研究施肥对土壤磷素状况的影响。结果表明,在紫色土上以化肥为基础增施有机肥(泥炭或菜籽粕)既提高土壤磷含量,又增加无机磷组分中有效磷源和缓效磷源的比例,且不会增加磷素淋失的风险,是所有处理中最优者;增磷、增钾处理虽然提高了土壤磷含量,但未能提高速效磷源与缓效磷源的比例;增氮、增硼及常规施肥降低土壤磷含量和提高无效磷源的比例;无肥处理磷含量最低,无效磷源比例最高。紫色菜园土无机磷约为有机磷的4—6倍,无机磷各组分以钙磷为主,占I-P总量的60.89%—67.92%,显示紫色土风化程度较低。各形态磷素呈Ca10-P>Ca8-P>Fe-P≈Al-P≈OC-P>Ca2-P序列变化,其中Ca2-P和Al-P总共仅占无机磷总量的11.47%—19.43%,表明紫色土中对植物最有效的磷源不足;而Ca10-P和OC-P共占无机磷总量的42.48%—59.55%,意味着紫色土无机磷有一半左右是以作物不可利用的形态存在的。紫色土全磷与无机磷、有机磷、Ca2-P、Ca8-P、Al-P、Fe-P、OC-P及Ca10-P呈显著正相关;无机磷与多种形态磷呈显著正相关(除有机磷、Ca2-P、有效磷外);有机磷与全磷、Ca2-P显著正相关;有效磷与全磷、Ca2-P、Al-P、Fe-P显著正相关;无机磷组分间也都存在显著正相关关系(OC-P与Ca10-P间有极显著正相关,但它们与其它无机磷组分无相关性)。表明在土壤磷的整个循环系统中,不同组分无机磷与有机磷之间处于一个动态平衡中,它们之间存在着相互影响和制约。土壤pH与各形态磷关系密切。对土壤有效磷与无机磷组分间的关系进行系统分析,简单相关分析结果土壤有效磷与Ca2-P、Fe-P呈极显著正相关,与Al-P呈显著正相关,与Ca8-P、OC-P、Ca10-P正相关但不显著;通径分析结果对土壤有效磷直接影响较大的无机磷组分是Al-P、Ca8-P与Ca2-P,其中Ca8-P的直接影响为负效应;逐步回归分析结果与通径分析一致。综合分析得出,Ca2-P、Al-P是最有效的磷源,Fe-P、Ca8-P次之,Ca10-P与OC-P是非有效磷源。莴笋和白菜产量与紫色土壤Ca2-P、Ca8-P、Al-P、Fe-P呈显著正相关,与OC-P、Ca10-P无相关性。紫色土各形态无机磷与两种蔬菜产量的相关系数r大小依次为Ca2-P>Fe-P>AL-P>Ca8-P>Ca10-P>OC-P,这与各形态无机磷与有效磷简单相关分析的结果一致。     

Relationship between availability indices and plant uptake of nitrogen and phosphorus from organic products

A better knowledge of the plant-availability of nitrogen (N) and phosphorus (P) in organic products may help to improve the efficient use of these products as fertilizers. In the present study, availability indices for N and P of nine widely differing organic products obtained by different fractionation methods were compared with the plant uptake of N and P from these products. The fractionation methods included CaCl₂ extraction, thermal fractionation (heating of organic products), and pepsin extraction, for N, and extraction with diluted sulphuric acid, P-Bray-I, P-Olsen, and extraction using an iron oxide coated filter paper, for P. The results of pot experiments with ryegrass using a double-pot technique (Janssen, 1990) over 62 (N experiment) and 93 days (P experiment) were used as reference for plant-availabe N and P. The 0.01 M CaCl₂ extractable inorganic N reasonably predicted plant-available N only in organic products with a high inorganic N fraction. Thermal fractionation and pepsin extraction provided a reasonable index for mineralizable N in organic products having a high fraction of mineralizable N. Of the P fractionation methods, the extraction using iron oxide coated filter paper was the best indicator of plant-available P in the products.