Surface runoff phosphorus (P) loss in relation to phosphatase activity and soil P fractions in Florida sandy soils under citrus production

Phosphorus losses by surface runoff from agricultural lands have been of public concern due to increasing P contamination to surface waters. Five representative commercial citrus groves (C1-C5) located in South Florida were studied to evaluate the relationships between P fractions in soils, surface runoff P, and soil phosphatase activity. A modified Hedley P sequential fractionation procedure was employed to fractionate soil P. Soil P consisted of mainly organically- and Ca/Mg-bound P fractions. The organically-bound P (biological P, sum of organic P in the water, NaHCO₃ and NaOH extracts) was dominant in the acidic sandy soils from the C2 and C3 sites (18% and 24% of total soil P), whereas the Ca/Mg-bound P (HCl-extractable P) accounted for 45-60% of soil total P in the neutral and alkaline soils (C1, C4 and C5 soils). Plant-available P (sum of water and NaHCO₃ extractable P fractions) ranged from 27 to 61 mg P kg⁻¹ and decreased in the order of C3>C4>C1>C2>C5. The mean total P concentrations (TP) in surface runoff water samples ranged from 0.51 to 2.64 mg L⁻¹. Total P, total dissolved P (TDP), and PO₄³⁻-P in surface runoff were significantly correlated with soil biological P and plant-available P forms (p<0.01), suggesting that surface runoff P was directly derived from soil available P pools, including H₂O- and NaHCO₃- extractable inorganic P, water-soluble organic P, and NaHCO₃- and NaOH-extractable organic P fractions, which are readily mineralized by soil microorganisms and/or enzyme mediated processes. Soil neutral (55-190 mg phenol kg⁻¹ 3 h⁻¹) and natural (measured at soil pH) phosphatase activities (77-295 mg phenol kg⁻¹ 3 h⁻¹) were related to TP, TDP, and PO₄³⁻-P in surface runoff, and plant-available P and biological P forms in soils. These results indicate that there is a potential relationship between soil P availability and phosphatase activities, relating to P loss by surface runoff. Therefore, the neutral and natural phosphatase activities, especially the natural phosphatase activity, may serve as an index of surface runoff P loss potential and soil P availability.     

Intensive management of a bamboo forest significantly enhanced soil nutrient concentrations but decreased soil microbial biomass and enzyme activity: a long-term chronosequence study

Purpose

Intensive long-term management practices in forest ecosystems can markedly influence soils’ physicochemical and microbial properties. However, their effects on the magnitude of nutrient pools and activities of enzymes regarding nutrient cycling in subtropical forest soils remain unclear. This study aimed to examine effects of long-term intensive management (organic mulching and chemical fertilization) on concentrations of different C, N, and P fractions and activities of enzymes involved with nutrient cycling in a subtropical Lei bamboo (Phyllostachys violascens) forest soil.

Materials and methods

Soil samples were taken from a chronosequence of Lei bamboo forests with intensive management spanning 0, 5, 10, and 15 years. Concentrations of various forms of C, N, and P, as well as activities of β-glucosidase, cellobiohydrolase, urease, protease, and acid phosphatase were measured.

Results and discussion

The results revealed that the concentrations of different classes of C (water-soluble organic C, hot-water-soluble organic C, and readily oxidizable C), N (NH₄⁺-N, NO₃^?-N, and water-soluble organic N), and P [resin-inorganic P (P_i), NaHCO₃-P_i, NaHCO₃-organic P (P_o), NaOH-P_i, NaOH-P_o, HCl-P_i, and residual-P] were enhanced markedly with prolonged duration of intensive management. Furthermore, activities of β-glucosidase, cellobiohydrolase, urease, protease, and acid phosphatase were increased following a 5-year treatment, while they were markedly reduced from 5- to the 15-year treatments. The 15 years of intensive management significantly reduced microbial biomass C and N concentrations by 8.2% and 31.9%, respectively, compared to the control.

Conclusions

We concluded that long-term intensive management led to the accumulation of C, N, and P, while it negatively impacted microbial biomass and activities of enzymes involved in nutrient cycling in subtropical Lei bamboo forest soils. Consequently, a reduction in chemical fertilizers should be considered toward the long-term sustainable development of subtropical Lei bamboo forests.

     

Transformation of added phosphorus to acid upland soils with different soil properties in Indonesia

Abstract

The transformation of added phosphorus (P) to soil and the effect of soil properties on P transformations were investigated for 15 acid upland soils with different physicochemical properties from Indonesia. Based on oxide-related factor scores (aluminum (Al) plus 1/2 iron (Fe) (by ammonium oxalate), crystalline Al and Fe oxides, cation exchange capacity, and clay content) obtained from previous principal component analyses, soils were divided into two groups, namely Group 1 for soils with positive factor scores and Group 2 for those with negative factor scores. The amounts of soil P in different fractions were determined by: (i) resin strip in bicarbonate form in 30 mL distilled water followed by extraction with 0.5 mol L^?1 HCl (resin-P inorganic (P_i) that is readily available to plant), (ii) 0.5 mol L^?1 NaHCO₃ extracting P_{i and} P organic (P_o) (P which is strongly related to P uptake by plants and microbes and bound to mineral surface or precipitated Ca-P and Mg forms), (iii) 0.1 mol L^?1 NaOH extracting P_i and P_o (P which is more strongly held by chemisorption to Fe and Al components of soil surface) and (iv) 1 mol L^?1 HCl extracting P_i (Ca-P of low solubility). The transformation of added P (300 mg P kg^?1) into other fractions was studied by the recovery of P fractions after 1, 7, 30, and 90 d incubation. After 90 d incubation, most of the added P was transformed into NaOH-P_i fraction for soils of Group 1, while for soils of Group 2, it was transformed into resin-P_i, NaHCO₃-P_i and NaOH-P_i fractions in comparable amounts. The equilibrium of added P transformation was reached in 30 d incubation for soils of Group 1, while for soils of Group 2 it needed a longer time. Oxide-related factor scores were positively correlated with the rate constant (k) of P transformation and the recovery of NaOH-P_i. Additionally, not only the amount of but also the type (kaolinitic) of clay were positively correlated with the k value and P accumulation into NaOH-P_i. Soils developed from andesite and volcanic ash exhibited significantly higher NaOH-P_i than soils developed from granite, volcanic sediments and sedimentary rocks. Soil properties summarized as oxides-related factor, parent material, and clay mineralogy were concluded very important in assessing P transformation and P accumulation in acid upland soils in Indonesia.     

Stable Isotope (δ13C and δ15N) Signatures and Their Relationship among Soil Enzyme Activities in Indian Semi-arid Agricultural Soils

ABSTRACT

A field evaluation of the stable isotopes (δ¹³C and δ¹⁵N) and their relationship among physicochemical and enzyme activities was conducted in Indian semi-arid agricultural soils. Composite soil samples were collected based on organic management (ORG), inorganic management (IM), integrated crop management (ICM) and precision farming (PF) experimental plots from the fall of September 2017 to October 2018. δ¹⁵N was significantly higher (13.85 %) in ORG soils compared with ICM (13.28 %), IM (12.84 %) and PF (12.75 %). In contrast δ¹³C was higher (?13.25%) in PF soils than IM (?13.6 %), ICM (?15.07 %) and ORG (?15.23 %). Soils from ORG had significantly higher levels of total N, total C, total S, organic carbon, available N, extractable P, Soil organic carbon stock, exchangeable K and enzyme activities compared to IM, ICM and PF. Urease, β – glucosidase, acid phosphatase, alkaline phosphatase, invertase, cellulase and dehydrogenase activities significantly increased the δ¹⁵N and reduced δ¹³C in agricultural soils. Our results suggested that organic management had improved the δ¹⁵N, plant available nutrients and soil enzyme activities. Stable δ¹³C and δ¹⁵N isotopes are good indicators of monitor the soil health, carbon, and nitrogen biogeochemical cycles in Indian semi-arid agricultural soils.     

Distribution of Inorganic and Organic Phosphorus Fractions in Two Phosphorus-Deficient Soils as Affected by Crop Species and Nitrogen Applications

It is desirable to know the distribution of phosphorus (P) fractions in soil so that plants may use P efficiently. Here we report the dynamics of inorganic and organic P in P-deficient black and rice soil cropped by soybean, white lupin, and maize supplied with nitrogen (N) inputs by N fixation and urea fertilizer. Inorganic P fractions of the three cropped soils could be ranked as O-P (organic phosphorus) > Al-P (aluminum phosphorus) > Fe-P (iron phosphorus) > Ca₁₀-P (calcium-10 phosphorus) > Ca₈-P (calcium-8 phosphorus) > Ca₂-P (calcium-2 phosphorus), irrespective of soil type. The potential of various inorganic P fractions to plant nutrition differed between soybean and white lupin. The percentage of total P present as inorganic P was affected by crop, soil type, and N source. In black soil, the change of organic P fraction induced by N fixation was larger than by urea application. The moderately labile organic P (MLOP) concentration was not affected significantly by soil type and crop species, and it was probably the main P source to the inorganic P fraction because the correlation between the two pools was high (r = 0.945; P < 0.05). Crop species differed in their uptake of inorganic and organic P from soil. Though P fraction concentrations varied between black soil and rice soil, their response to crop species and N source was similar. The amounts of P removed from soil were affected by N source. The right choice of crop species and the application a suitable N source may increase crop yield and P uptake by plant in P-deficient soils.     

Effects of phosphorus addition and energy supply on acid phosphatase production and activity in soils

To find out how acid phosphatase activity and production in some Alberta soils may be related to soil properties and past fertilizer history, soils of varying organic matter content, extractable P and P fertilization history were assayed for acid phosphatase using p-nitrophenyl phosphate as substrate. The effect of solution P concentration during the phosphatase assay was examined. The effect of P on the production of new phosphatase was examined in soils incubated with an added energy supply or orthophosphate.Phosphatase activity was influenced by P fertilization practices during the 5 yr before sampling. In a Black Chernozemic soil (Malmo SiCL) with a high organic matter content and high initial phosphatase activity, P fertilization at 27 or 54 kg P ha^?1 y^?1 for 5 yr reduced phosphatase activity by about 20%. However, in a Grey Luvisolic soil (Cooking Lake L) with low organic matter and initial phosphatase, P fertilization at 54 kg P ha^?1y^?1 for 5 yr tended to increase activity, probably by increasing plant root growth and organic matter additions.Assay solutions containing orthophosphate at 0.55 mM reduced activity by 25% and 47% in a Malmo SiCL and Maleb L (Orthic Brown Chernozem) soil respectively. Further increases of phosphate concentration to 5.5 mM reduced phosphatase activity by 50% and 76% in the Malmo and Maleb L soils respectively.Phosphatase activity was increased up to 6-fold by incubation of soil with glucose and NH₄NO₃. Addition of P to produce an added C: added P ratio of 20:1 completely prevented synthesis of phosphatase by proliferating organisms and had a slight inhibitory effect on phosphatase already present. Similarly, addition of P without C in a 6-week incubation had only a small effect on phosphatase activity and maintained P concentrations in the assay solutions slightly below 0.55 mM. It was concluded that the effect of phosphate on soil phosphatase operates more through its effect on phosphatase synthesis than on activity of existing phosphatase.     

Mycorrhizal (Rhizophagus Intraradices) Symbiosis and Fe and Zn Availability in Calcareous Soil

Greenhouse experiment was conducted to assess the iron (Fe) and zinc (Zn) fractionation patterns in soils of arbuscular mycorrhizal (AM) fungus-inoculated and uninoculated maize plants fertilized with varying levels of Fe and Zn. Soil samples were collected for Fe and Zn fractions and available Fe, Zn and phosphorus (P) contents besides organic and biomass carbon (BMC), soil enzymes and glomalin. Major portion of Fe and Zn fractionations was found to occur in the residual form. Mycorrhizal symbiosis increased the organically bound forms of Fe and Zn while reducing the crystalline oxide, residual Fe and Zn fractions, indicating the transformation of unavailable forms into available forms. Soil enzymes, viz. dehydrogenase and acid phosphatase activities in M+ soils, were significantly higher than M? soil consistently. Overall, the data suggest that mycorrhizal symbiosis enhanced the availability of Fe and Zn as a result of preferential fractionation and biochemical changes that may alleviate micronutrient deficiencies in calcareous soil.

Abbreviations: AM: arbuscular mycorrhiza; Fe: Iron; Zn: Zinc; P: Phosphorous; Amox-Zn: amorphous oxide bound zinc; Cryox-Zn: crystalline oxide bound zinc; DAS: days after sowing; DTPA: diethylene Triamine Penta Acetic Acid; MnO₂-Zn: manganese oxide bound zinc; OC-Zn: organically bound zinc; WSEX: water soluble plus exchangeable zinc; MnO₂ Fe: manganese oxide bound iron; OC-Fe: Organically bound iron; WSEX Fe: water soluble plus exchangeable iron.     

Growth,phosphorus uptake,and rhizosphere microbial‐community composition of a phosphorus‐efficient wheat cultivar in soils differing in pH

In a pot experiment, the P‐efficient wheat (Triticum aestivum L.) cultivar Goldmark was grown in ten soils from South Australia covering a wide range of pH (four acidic, two neutral, and four alkaline soils) with low to moderate P availability. Phosphorus (100 mg P kg^–1) was supplied as FePO₄ to acidic soils, CaHPO₄ to alkaline, and 1:1 mixture of FePO₄ and CaHPO₄ to neutral soils. Phosphorus uptake was correlated with P availability measured by anion‐exchange resin and microbial biomass P in the rhizosphere. Growth and P uptake were best in the neutral soils, lower in the acidic, and poorest in the alkaline soils. The good growth in the neutral soils could be explained by a combination of extensive soil exploitation by the roots and high phosphatase activity in the rhizosphere, indicating microbial facilitation of organic‐P mineralization. The plant effect (soil exploitation by roots) appeared to dominate in the acidic soils. Alkaline phosphatase and diesterase activities in acidic soils were lower than in neutral soils, but strongly increased in the rhizosphere compared with the bulk soil, suggesting that microorganisms contribute to P uptake in these acidic soils. Shoot and root growth and P uptake per unit root length were lowest in the alkaline soils. Despite high alkaline phosphatase and diesterase activities in the alkaline soils, microbial biomass P was low, suggesting that the enzymes could not mineralize sufficient organic P to meet the demands of plants and microorganisms. Microbial‐community composition, assessed by fatty acid methylester (FAME) analysis, was strongly dependent on soil pH, whereas other soil properties (organic‐C or CaCO₃ content) were less important or not important at all (soil texture).     

模拟氮沉降对湿性常绿阔叶次生林土壤碳氮组分和酶活性的影响

为了研究氮沉降对次生林土壤碳氮组分和酶活性的影响,以华西雨屏区湿性常绿阔叶次生林为对象,从2014年1月起进行野外定位模拟氮沉降试验,分别设置对照(CK,+0 g/(m^2·a))、低氮(LN,+5 g/(m^2·a))和高氮(HN,+15 g/(m^2·a))3个氮添加水平。在氮沉降进行27个月后,按照腐殖质层和淋溶层表层进行取样,测定不同土层土壤总有机碳(TOC)、可浸提溶解性有机碳(EDOC)、易氧化碳(ROC)、全氮(TN)、硝态氮(NO_3^-—N)和铵态氮(NH_4^+—N)含量以及蔗糖酶、脲酶、酸性磷酸酶和多酚氧化酶活性。结果表明:模拟氮沉降显著增加该次生林腐殖质层土壤的TOC和NH_4^+—N含量,显著增加腐殖质层和淋溶层表层土壤的NO_3^-—N含量,腐殖质层土壤C/N显著升高。淋溶层表层土壤TOC、NH_4^+—N、C/N以及2层土壤的EDOC、ROC、TN和NH_4^+—N/NO_3^-—N均无显著影响。2层土壤的多酚氧化酶活性均随着氮添加量的升高而降低,其中淋溶层表层达到显著差异。模拟氮沉降对蔗糖酶、脲酶和酸性磷酸酶活性均无显著影响。腐殖质层中,NH_4^+—N和NO_3^-—N含量与TOC含量存在极显著正相关关系。2层土壤的多酚氧化酶活性均与NO_3^-—N含量呈极显著负相关。结果说明,模拟氮沉降使该次生林中原本较高的腐殖质层土壤TOC含量进一步显著增加,并且促进土壤无机氮的积累,而模拟氮沉降对多酚氧化酶的抑制作用更加有利于土壤有机质的积累。     

Phosphatase activity in Nasutitermes ephratae termite nests

Summary The relationship between phosphatase activity and soil was studied in 14 mounds and adjacent control soils of plant debris-feeding termites from a Venezuelan savanna. The soils were assayed for acid phosphatase activity with p-nitrophenyl phosphate as substrate and for the effect of inorganic P (300 g P g^–1). The proportion of organic matter in the mounds was four times that found in topsoils, indicating strong selection by the termites for organic-rich soil fractions. A comparison of phosphatase activities found no difference between mounds and adjacent soils. It seems possible that the expected increase of enzyme activity in mounds, due to a higher C content, was counteracted by enzyme inhibition due to higher levels of available inorganic P in the mounds. Addition of inorganic P to soil and mound material reduced enzyme activities by 10%–45%, but after a 2-day incubation period differences between the treated soil and the control tended to disappear.     

Biodegradation of low molecular weight organic acids in rhizosphere soils from a tropical montane rain forest

Root exudation of organic acids could be an important strategy for plant acquisition of phosphorus (P) from P-deficient soils in tropical rain forests. However, the efficacy of organic acids on P mobilization in the rhizosphere could be reduced due to their rapid biodegradation by rhizosphere microorganisms. To assess the dynamics and function of organic acids in the rhizosphere soils in tropical rain forests, we examined the concentrations of oxalate, citrate, and malate in soil solution and the mineralization kinetics of ¹⁴C-radiolabelled oxalate and citrate in the rhizosphere and bulk soil fractions. We compared two tropical montane rain forests from Mt. Kinabalu, Borneo that share similar parent material (i.e., sedimentary rocks) and climate but differ in terms of soil age. The older soil (Tertiary age materials) was affected by podzolization and had less inorganic labile P compared to the younger soil (Quaternary colluvial deposits). In the P-deficient older soil, the rhizosphere soil solution contained markedly higher concentrations of oxalate, citrate, and malate than did the bulk soil, whereas in the P-rich younger soil, the levels of organic acids in the rhizosphere were lower. The higher levels of organic acids in the rhizosphere of P-deficient soils are caused by greater root exudation and the lower sorption capacity for organic acids. The results of mineralization kinetics showed that oxalate and citrate in soil solution were rapidly mineralized in both rhizosphere and bulk fractions of both P-rich and P-deficient soils, having short mean residence times (2.3–13.1 h for oxalate and 0.8–1.6 h for citrate). The mineralization rates of oxalate and citrate were highest in the rhizosphere fraction of the P-deficient soil, where the pool of organic acids was largest and rapidly replenished by root exudation. Our data indicate that consumption as well as production of organic acids in the rhizosphere could be enhanced in P-deficient soil. The efficacy of organic acids on P mobilization in the rhizosphere in tropical montane rain forests appears to vary depending on the level of soil P availability and the anion sorption capacity, attributable to soil aging with podzolization.     

Rice-residue biochar influences phosphorus availability in soil with contrasting P status

ABSTRACT

Thermo-chemical conversion of crop residues to produce biochar is an emerging strategy in the context of sustainable phosphorous (P) use and residue management. An incubation study for 90 d was conducted to investigate the effects of rice-residue biochar (0, 10, 20 and 40 g kg^?1) in combination with inorganic-P (KH₂PO₄) (0, 25 and 50 mg kg^?1) on phosphorous availability in medium- and high-P status soils. Increasing biochar addition rates alone or in combination with inorganic-P resulted in a significant increase in P pools, i.e. plant available P or Olsen-P (from 8 to 132 mg kg^?1 in medium-P and 15 to 160 mg kg^?1 in high-P soils), microbial biomass P and various mineral-bound inorganic-P fractions in the order (Ca-P > organic-P > Al-P > loosely held/soluble-P > Fe-P > reductant soluble-P). Further, lower phosphatase activity (19–50%) with increasing rates of biochar addition in both soils elucidates the ability of biochar to act as a long-term source of available P in the experimental soils. The results demonstrate that rice-residue biochar can directly or indirectly enhance the status of available P in soils and hence can be used as a beneficial amendment to meet the crop P demand.     

Distribution of exudates of lupin roots in the rhizosphere under phosphorus deficient conditions

Abstract

The distribution of secretory acid phosphatase and organic acids enhanced by phosphorus deficiency in lupin rhizosphere was investigated using a rhizobox system which separated the rhizosphere soil into 0.5 mm fractions. In the soil fraction closest to the root surface, the lupin exudates displayed an acid phosphatase activity of 0.73 u g^?1 dry soil and citrate concentration of 85.2 μmol g^?1 dry soil, respectively. The increase of the acid phosphatase activity-induced an appreciable depletion of organic P in the rhizosphere, indicating that lupin efficiently utilized the organic P from soil through the enzyme activitye The sterile treatments demonstrated that the acid phosphatase in the rhizosphere was mainly derived from lupin root secretions. The secretory organic acids enhanced considerably the solubility of the inorganic P in three types of soil and a sludge. However, the secretory acid phosphatase and organic acids from lupin roots were only detected in a considerable amount in 0-2.5 mm soil fractions from root surface.     

Phosphate sorption characteristics of major soils in Okinawa,Japan

Abstract

Phosphate sorption isotherms were determined for 16 representative major soils developed from different parent materials on Okinawa. Phosphate sorption characteristics were satisfactorily described by the Langmuir equation, which was used to determine phosphorus (P) sorption maxima of the soils. Phosphate sorption maxima ranged from 630 to 2208 mg P kg^‐1 soil (mean 1,362 mg P kg^‐1). The standard P requirement (i.e., the amount of P required to attain 0.2 mg P L^‐1 equilibrium solution) followed the same trend as sorption maximum (r =0.94***), with values ranging from 132 to 1,020 mg P kg^‐1 soil (mean 615 mg P kg^‐1). This mean value corresponds to fertilizer addition of 923 kg P ha^‐1 indicating that the soils have high P fertilizer requirements. Results of simple linear regression analysis indicated that sorption maximum was significantly correlated with clay content, organic matter, oxalate iron (Fe), pyrophosphate Fe, DCB aluminum (Al), oxalate Al, and pyrophosphate Al, but not with DCB Fe, pH, or available P content. The best regression model for predicting sorption maximum was the combination of clay, organic matter, pyrophosphate Fe, and DCB Al which altogether explained 79% of the variance in sorption maximum. The equation obtained could offer a rapid estimation of P sorption in Okinawan soils.     

STUDIES ON THE DECOMPOSITION OF PLANT MATERIAL IN SOIL

The organic matter in soils containing decomposing ¹⁴C-labelled ryegrass was fractionated chemically. Earlier work on these soils had shown that they contained a small fraction, heavily labelled relative to the rest of the soil organic matter, that was mineralized when the partially sterilized soils were incubated. Reagents effective in extracting heavily labelled-C included cold o.in HC1, boiling saturated CaSO₄ solution, and o.in Ba(OH)₂, but neither these nor any other reagent tested could extract material as heavily labelled as that mineralized when partially sterilized soil was incubated. Reagents that extract heavily labelled-C are poor extractants for humified material and are not strongly hydrolytic: the more vigorous the hydrolysis the smaller the proportion of labelled-C in the hydrolysate. The amounts of labelled-C dissolved by Ba(OH)₂ from soils sampled after different periods in the field were directly proportional to the amounts of labelled-C mineralized by those soils when partially sterilized (by exposure to CHC1₃ vapour), inoculated and incubated. Balance sheets are presented for the distribution of labelled and unlabelled-C in fractions separated by hydrolysis with 6N HC1, by NaOH extraction, by neutral pyrophosphate extraction, and by oxidation with H₂O₂. The fraction remaining after hydrolysis with 6N HC1 was the most lightly labelled and had the widest C/N ratio. The percentage of labelled-C in the material dissolved by alkali or by pyrophosphate was little more than in the material not dissolved, despite the presence in the soil of fractions differing at least twenty-fold in intensity of labelling.     

Phosphatase activity and phosphorus fractions in Karri (Eucalyptus diversicolor F. Muell.) forest soils

Summary Karri forest soils contain negligible concentrations of labile-P, low concentrations of total P and more P in organic forms than inorganic. The ratio of organic P to inorganic P was lowest (1:2) in recently burnt surface soils and greatest (7:1) at depth in soil that had been undisturbed for long periods of time. Phosphomonoesterase and phosphodiesterase activities (to 10 cm depth, phosphomonoesterase 700–1300; phosphodiesterase 2000–2400 g nitrophenol released h^-1 g^-1 fresh weight) were comparable to those in other, organically rich forest soils. The optimum pH for phosphatase activities were within 1–2 units of soil pH (6) and little reduction in activity was observed over the pH range 4–8. Phosphatase activity was reduced by air-drying (up to 20-fold reduction) and was almost entirely absent in soils that were heat-affected as a result of logging/burning operations. Neither phosphomonoesterase nor phosphodiesterase were directly related to soil P fractions or total P. A reduction in P demand is postulated as the cause of reduced phosphatase activity and the increased concentration of organic P with increasing soil depth.     

不同林龄杉木林下套种阔叶树对土壤磷组分的影响

套种是杉木人工林经营的重要措施,磷是南方森林生态系统中主要限制性养分元素之一,但套种模式对土壤磷素的影响尚不明确。以亚热带杉木人工林表层(0-10 cm)土壤为对象,研究套种林(杉阔套种幼林、杉阔套种成熟林)和杉木幼林土壤理化性质和土壤各形态磷含量差异,分析套种对杉木人工林土壤磷含量的影响。结果表明:(1)不同套种林显著改变土壤总磷、土壤总无机磷、土壤总有机磷、土壤微生物生物量磷(MBP)和土壤酸性磷酸酶活性(APA),大小顺序均为杉阔套种成熟林>杉阔套种幼林>杉木幼林。(2)土壤各磷组分中活性磷含量较低,其中NaHCO3-Po在活性组分中占主导;土壤NaOH-Po是中等活性磷的主要组分,杉阔套种成熟林尤为显著;闭蓄态磷(Residual-P)在总磷含量中最高。(3)与杉木幼林相比,杉阔套种成熟林显著增加了树脂提取态磷(Resin-Pi)、碳酸氢钠提取态有机和无机磷(NaHCO3-Pi、NaHCO3-Po)、氢氧化钠提取态有机和无机磷(NaOH-Pi、NaOH-Po)、氢氧化钠残留提取态有机磷(NaOHu.s-Po)、盐酸提取态磷(HCl-Pi)和闭蓄态磷(Residual-P)含量;土壤总无机磷、NaHCO3-Po、HCl-Pi、NaHCO3-Pi、NaOHu.s-Pi和Residual-P对杉阔套种幼林的响应不敏感。(4)除含水率外不同林龄下杉阔套种林土壤磷形态与土壤理化性质(土壤总碳氮、土壤可溶性有机氮、土壤微生物生物量磷、酸性磷酸酶)呈正相关性(P<0.05)。冗余分析表明,土壤磷组分的变化主要受MBP调控,且MBP与有机磷组分(NaOHu.s-Po、NaOH-Po)和HCI-Pi呈显著正相关。总之,套种林的土壤磷素有效性高于杉木幼林,土壤养分状况更佳。     

Mobile and readily available C and N fractions and their relationship to microbial biomass and selected enzyme activities in a sandy soil under different management systems

Within different land‐use systems such as agriculture, forestry, and fallow, the different morphology and physiology of the plants, together with their specific management, lead to a system‐typical set of ecological conditions in the soil. The response of total, mobile, and easily available C and N fractions, microbial biomass, and enzyme activities involved in C and N cycling to different soil management was investigated in a sandy soil at a field study at Riesa, Northeastern Germany. The management systems included agricultural management (AM), succession fallow (SF), and forest management (FM). Samples of the mineral soil (0—5, 5—10, and 10—30 cm) were taken in spring 1999 and analyzed for their contents on organic C, total N, NH₄⁺‐N and NO₃^—‐N, KCl‐extractable organic C and N fractions (Corg_(KCl) and Norg_(KCl)), microbial biomass C and N, and activities of β‐glucosidase and L‐asparaginase. With the exception of Norg_(KCl), all investigated C and N pools showed a clear relationship to the land‐use system that was most pronounced in the 0—5 cm profile increment. SF resulted in greater contents of readily available C (Corg_(KCl)), NH₄⁺‐N, microbial biomass C and N, and enzyme activities in the uppermost 5 cm of the soil compared to all other systems studied. These differences were significant at P ≤ 0.05 to P ≤ 0.001. Comparably high C_mic:C_org ratios of 2.4 to 3.9 % in the SF plot imply a faster C and N turnover than in AM and FM plots. Forest management led to 1.5‐ to 2‐fold larger organic C contents compared to SF and AM plots, respectively. High organic C contents were coupled with low microbial biomass C (78 μg g^—1) and N contents (10.7 μg g^—1), extremely low C_mic : C_org ratios (0.2—0.6 %) and low β‐glucosidase (81 μg PN g^—1 h^—1) and L‐asparaginase (7.3 μg NH₄‐N g^—1 2 h^—1) activities. These results indicate a severe inhibition of mineralization processes in soils under locust stands. Under agricultural management, chemical and biological parameters expressed medium values with exception for NO₃^—‐N contents which were significantly higher than in SF and FM plots (P ≤ 0.005) and increased with increasing soil depth. Nevertheless, the depth gradient found for all studied parameters was most pronounced in soils under SF. Microbial biomass C and N were correlated to β‐glucosidase and L‐asparaginase activity (r ≥ 0.63; P ≤ 0.001). Furthermore, microbial biomass and enzyme activities were related to the amounts of readily mineralizable organic C (i.e. Corg_(KCl)) with r ≥ 0.41 (P ≤ 0.01), suggesting that (1) KCl‐extractable organic C compounds from field‐fresh prepared soils represent an important C source for soil microbial populations, and (2) that microbial biomass is an important source for enzymes in soil. The Norg_(KCl) pool is not necessarily related to the size of microbial biomass C and N and enzyme activities in soil.<?show $6#>     

Role of Phenolics and Organic Acids in Phosphorus Mobilization in Calcareous and Acidic Soils

Abstract

Phenolic acids (caffeic, CAF; protocatechuic, PCA; p-coumaric, COU; and vanillic, VAN), catechol (CAT), poly-galacturonic acid (PGA), and citric acid (CIT) were compared for their effectiveness in phosphorus (P) mobilization in three soils differing in chemical properties. The addition of organic ligands at 100 μmol g^{? 1} soil increased the concentrations of resin P (P_r), water-extractable P (P_w), and bicarbonate-extractable inorganic P (P_bi), thus improving the phosphorus availability. The magnitude of P mobilization in the calcareous soil can be expressed in the following order: CAF > CAT > PCA = CIT > VAN > COU > PGA, which was consistent with the number of phenolic hydroxyl groups they contained and the position of carboxyl on the benzoic ring. In the two acid soils tested, the order of P mobilization was CIT > CAT > PCA > CAF after 24 h incubation, and CIT > PCA > CAF > CAT after a 14 d incubation. The mobilized P originated partly from the organic P fractions, which could be extracted by 0.5 M NaHCO₃. In addition, P_r decreased and P_w increased during incubation. The exceptions were that the CAF treatment increased P_r and the CIT treatment did not affect P_w. Calcium extraction from the soils after a 1 d or 14 d incubation could not fully account for the P mobilization. The results suggest that the inorganic P dissolution by the organic ligands was not the only mechanism of P mobilization in the calcareous soil, while in acid soils the chelation of metal cations by organic ligands is likely an important factor in P mobilization.     

Microbiological Properties in Earthworm Cast and Surrounding Soil Amended with Various Organic Wastes

Abstract

Changes produced in the microbiological properties of earthworm Lumbricus terrestris casts and surrounding soil by the addition of various organic wastes such as wheat straw (WS), tea production waste (TEW), tobacco production waste (TOW), cow manure (CM), and hazelnut husk (HH) were evaluated in an incubation experiment. Twenty‐one days after organic waste treatment, analyses of microbial biomass (Cmic), basal soil respiration (BSR), metabolic quotient (qCO₂), and enzyme activities (dehydrogenase, catalase, β‐glucosidase, urease, alkaline phosphatase, and arylsulphatase) were carried out on collected cast and soil samples. Addition of organic wastes to the soil increased values of Cmic, BSR, and enzyme activities in soil and earthworm casts, indicating activation by microorganisms. Except for catalase activity, these values of microbiological parameters in casts were higher than in surrounding soil at all waste treatments and control. The addition of organic wastes caused a rapid and significant increase in organic carbon, total nitrogen, and microbiological properties in both soils; this increase was especially noticeable in soils treated with TEW.