菜园土壤有效钾提取方法比较研究——以重庆地区为例

研究菜园土壤有效钾的测定方法,为蔬菜合理施用钾肥提供理论依据。以36个莴笋钾肥田间试验的产量及吸钾量为参比标准,采用7种方法 (醋酸铵法、ASI法、Mehlich3法、冷硝酸法、四苯硼钠法1、四苯硼钠法2和沸硝酸法)测定土壤有效钾含量。结果表明,土壤有效钾含量以沸硝酸法四苯硼钠法2四苯硼钠法1冷硝酸法Mehlich3法醋酸铵法ASI法。7种测定方法测得的土壤有效钾含量间呈不同程度正相关,均具有评价土壤钾素有效性的潜力。四苯硼钠法1和四苯硼钠法2测得的土壤有效钾含量与无肥区占施钾区莴笋相对产量(RY_(CK))、缺钾区占施钾区莴笋相对产量(RY_(NP))、无肥区占施钾区莴笋相对吸钾量(RUK_(CK))的相关性均达显著水平,即其测得的土壤钾素的生物有效性均较好。综合而言,在所试验土壤地区,四苯硼钠法1和四苯硼钠法2均是评价菜园土壤当季钾素有效性的较好方法,其中以四苯硼钠法1更好。     

安徽省油菜钾肥施用效果及土壤速效钾丰缺指标研究

2005—2009连续4个年度在安徽省冬油菜生产区布置油菜钾肥肥效试验73个,研究施用钾肥对油菜产量和经济效益的影响;并通过建立油菜籽粒相对产量和土壤速效钾含量的关系,确定土壤速效钾丰缺指标。结果表明,油菜施用钾肥具有明显的增产效果,施钾后油菜平均产量达2 558 kg/hm~2,比不施钾增产509 kg/hm~2,增产率为28.1%。施钾每公顷平均增收1 349元,67.1%的试验点产投比2.0,施钾收益显著。13.7%的试验点施钾后增产不增收。以相对产量60%、60%~75%、75%~90%、90%~95%和95%为标准,将土壤速效钾分为"严重缺乏"、"缺乏"、"轻度缺乏"、"适宜"和"丰富"5个等级,处于各等级的土壤面积的比例分别为2.7%、17.8%、65.8%、6.8%和6.8%,对应的丰缺指标分别为30、30~60、60~110、110~140和140 mg/kg。此研究建立的土壤速效钾丰缺指标可为安徽省冬油菜的钾肥管理提供依据。     

常规浸提剂与联合浸提剂测定我国北方石灰性土壤有效磷钾的比较

使用常规浸提剂与两种联合浸提剂Mehlich 3(M3)、ASI分别测定了中国8个地区10种土壤样品的有效磷、速效钾含量,分析比较了常规浸提剂与两种联合浸提剂测定土壤有效磷速效钾的差异性及相关性。统计分析表明,对于有效磷,M3、ASI两种联合浸提剂的浸提结果均大于常规浸提剂的浸提结果,且M3浸提剂浸提结果的变幅较常规浸提剂浸提结果相对较小,而精确度较高。相关分析表明,常规浸提结果与M3浸提结果呈极显著正相关(P<0.01),相关系数为0.680。对于速效钾,M3浸提剂的浸提量较常规浸提剂相近,常规浸提量与M3浸提量呈极显著正相关(P<0.01),相关系数为0.996。综合而言,M3这种联合浸提剂是测定土壤有效磷、速效钾的理想浸提方法。     

土壤养分有效性测定及其方法

在提出土壤养分有效性测定概念的基础上 ,本文对各种土壤养分有效性的测定方法进行了总结 ,讨论了这些方法的测定机理、测定效果及近几年的进展。这些方法包括用于磷钾等元素测定的树脂法、用于氮测定的生物培养法和化学提取法、磷测定的氧化铁试纸法和氢氧化铁透析管法和钾的四苯硼钠法     

不同有效钾提取方法的原理与效率比较

以6种典型含钾矿物为研究对象,探讨了盐溶液提取法、阳离子交换树脂法及四苯硼钠法等不同有效钾提取方法的原理、效率及影响因素的影响效应和机制。结果表明：盐溶液提取法对含钾矿物中钾的提取能力受离子种类、浓度及pH的影响,不同种类盐提取剂对矿物中钾释放的促进作用也因含钾矿物类型而异。NH4+ 使矿物层间塌陷,显著抑制各种矿物中非交换态钾的释放。阳离子交换树脂法对溶液中钾的提取能力与饱和离子种类及振荡强度有关。H+、Na+ 饱和树脂吸附溶液钾的能力大于Ca2+ 饱和树脂。振荡强度选为120 r/min可消除树脂法提取钾素时液膜扩散阻力的干扰。四苯硼钾的溶度积常数Ksp为2.40 × 10-8（25℃）。不加NaCl条件下,四苯硼钠浓度是影响四苯硼钠法对含钾矿物中钾的提取能力的主要因素。由不同方法的提取原理可以看出,铵盐类提取剂适用于速效钾为当季作物主要钾源（速效钾含量较高）的土壤钾素有效性的评价。而其他盐提取剂通过延长提取时间,可提取部分非交换态钾,可能较醋酸铵法更适合于提取非交换态钾为当季作物主要钾源的土壤有效钾。阳离子交换树脂法也可提取土壤非交换态钾,但操作较为繁琐,该方法更适用于原位研究土壤钾素的迁移、扩散等特性。四苯硼钠法提取效率较高,通过调节其提取力,可提取不同程度的非交换态钾,是具有较好应用前景的适于各类土壤和作物的土壤有效钾测定方法。     

美国中南部土壤磷钾丰缺指标体系及其施肥推荐

对美国中南部有代表性的7个州(俄克拉荷马、阿肯色、德克萨斯、路易斯安那、堪萨斯、爱荷华、北卡罗来纳)的最新的土壤磷钾丰缺指标体系和主要作物的磷钾施肥推荐量进行了研究与整理,旨在对我国的测土配方施肥工作有所启迪。     

土壤有效钾提取方法评价

本文综述了土壤有效钾的提取方法,并根据不同浸提方法的测定结果与作物反应与标准方法之间的相关性进行了评价。结果表明有多种方法与参比项有显著的相关性。并推荐单独提取土壤有效钾时用1moL·l-1中性NH4OAC法,也可用CEM法或2moL·l-1冷HNO3法,同时需要提取其他有效养分时可用ASI法或M-3法。个别土壤还可用其他方法。但在石灰性土壤上不能用Bray-1法和M-1法。     

山西石灰性土壤速效磷、钾测定方法的比较

用M ehlich3通用浸提剂法对山西石灰性土壤速效磷、钾的含量进行了测定,并与常规方法进行比较。结果表明:M ehlich3法与常规土壤速效磷、钾测定方法的测定结果呈显著正相关性。磷的替代性较差,钾的替代性较好,且两元素之间可以相互换算。     

Influence of soil ingestion by earthworms on the availability of potassium in soil: An incubation experiment

Summary An incubation experiment was conducted to study the changes that occur in the K status of soil due to earthworm activity. Samples of Tokomaru silt loam soil were inoculated with the common pasture earthworm species Aporrectodea caliginosa and incubated for 21 days. Aliquots of moist soil were analyzed for exchangeable K by leaching with neutral molar ammonium acetate at 1:50 soil solution ratio. Extraction with boiling 1 M nitric acid at 1:100 soil solution ratio for 20 min was used to determine available non-exchangeable K. The results indicated that the exchangeable K content increased significantly due to earthworm activity but nitric acid-extractable K did not change significantly. It is inferred that earthworms increase the availability of K by shifting the equilibrium among the forms of K from relatively un-available forms to more available forms in the soil chosen for the study.     

土壤非交换态钾与结构态钾能够区分吗？

Nonexchangeable K (NEK) is the major portion of the reserve of available K in soil and a primary factor in determining soil K fertility. The questions of how much NEK is in soils and how to quantify total NEK in soils are so far still unclear due to the complicated effects of various minerals on K fixation. In this study, the NEK in 9 soils was extracted with sodium tetraphenylboron (NaBPh₄) for various time periods longer than 1 d. The results showed that the NEK extracted by NaBPh₄ gradually increased with time, but showed no more increase after the duration of extraction exceeded 10--20 d. As the temperature increased from 25 to 45 ^oC, the duration to obtain the maximum extraction of NEK was reduced from 20 to 10 d, and the maximum values of NEK released at both temperatures was almost the same for each soil. The maximum NEK (MNEK) of the 9 soils extracted by NaBPh4 varied from 3 074 to 10 081 mg kg^-1, accounting for 21%--56% of the total soil K. There was no significant correlation between MNEK released by NaBPh₄ and other forms of K, such as NH₄OAc-extracted K, HNO₃-extracted K and total K in soils, which indicates that NEK is a special form of K that has no inevitable relationship to the other forms of K in soils. The MNEK extraction by NaBPh₄ in this study indicated that the total NEK in the soils could be differentiated from soil structural K and quantified with the modified NaBPh₄ method. The high MNEK in soils made NEK much more important in the role of the plant-available K pool. How to fractionate NEK into different fractions and establish the methods to quantify each NEK fraction according to their bioavailability is of great importance for future research.     

Comparison of chemical methods of assessing potentially available organic nitrogen in soil

Abstract

We recently developed two rapid and precise chemical methods of assessing potentially available organic N in soils. One method involves determination of the ammonia‐N produced by steam distillation of the soil sample with pH 11.2 phosphate‐borate buffer solution for 8 min. The other involves determination of the ammonium‐N produced by treatment of the soil sample with 2M KCl solution at 100°C for 4 hours. Studies using 33 Brazilian soils showed that the results obtained by these methods were highly correlated with those obtained by anaerobic and aerobic incubation methods of assessing potentially available organic N in soil.

The two methods were further evaluated by applying them to 30 Iowa soils and by comparing their results and those obtained by other chemical methods with the results of the incubation methods considered to be the best laboratory methods currently available for assessment of potentially available organic N in soil. The chemical methods used included the acid KMnO₄ method, the alkaline KMnO₄ method, the CaCl₂‐autoclave method, and the NaHCO₃ UV method. The incubation methods used involved determination of the ammonium‐N produced by incubation of the soil sample under anaerobic conditions for 1 week or determination of the (ammonium + nitrate + nitrite)‐N produced by incubation of the sample under aerobic conditions for 2 and 12 weeks. The data obtained showed that the results of the two chemical methods evaluated were highly correlated with those obtained by the incubation techniques used for comparison and that the correlations observed with these two methods were higher than those observed with the previously proposed chemical methods. It is concluded that these two rapid and simple methods are the best chemical methods thus far developed for laboratory assessment of potentially available organic N in soil.     

Mehlich 3法与常规分析方法在测定土壤有效P、K的比较研究

采用Mehlich 3法和常规分析方法测定赤红土和红土的有效磷、有效钾,结果表明,Mehlich 3法测得的有效磷、有效钾与常规方法测定的呈显著的相关。赤红土上的玉米生物试验结果表明:Mehilch 3法测定的土壤有效磷、有效钾含量与玉米吸收的磷、钾量以及玉米的株高、干重呈显著相关。     

Applied Mn extracted by four methods correlated with Mn concentrations in soybean leaf tissue on a southeastern soil

Abstract

Four extractants for soil Mn were compared for their sensitivity to changes in Mn availability caused by rates and sources of added soil Mn and soil pH variations. Their ability to extract amounts of Mn correlated with plant Mn concentrations was also determined. Two field experiments were conducted on a sandy, high water table soil (Ultic Haplaquod‐Arenic Plinthaquic Paleudult) which included 5 Mn rates, 4 Mn sources and 3 soil pH levels. Soybeans [Glycine max (L.) Merr. cultivar Ransom] were grown and leaf tissue and soils sampled at the late pod‐fill stage. All four extractants separated the high‐ Mn rates, but the small exchange method did not separate the low Mn rates. Few differences were observed among extractants due to Ma sources. The DTPA method was the only procedure to correctly distinguish soil pH levels by showing decreasing extractable Ma with increasing soil pH. Including pH in multiple regressions significantly increased the plant Mn‐soil Mn correlation coefficients. The DTPA method and the 0.1N H₃PO₄ method had the highest correlation coefficients and the double acid method the lowest. The small exchange method was intermediate. Considering all the results, the DTPA was the most promising method for extracting Mn from this sandy, southern Coastal Plain soil.     

Ability of different soil extraction methods to predict potassium release from soil in ley over three consecutive years

To avoid over‐fertilization of potassium (K) and thereby a mineral composition in the grass crop not optimal for animal health, estimation of K release from soil is important. The analytical methods should therefore predict the total K release. Furthermore, to minimize costs for the farmers they should provide information which remains valid over a period of several years. The relationship between different soil extraction procedures for K and K uptake in ley for three subsequent years after soil sampling was studied in 19 field experiments on a range of mineral soil types in Norway. Potassium determined with solutions that extracted exchangeable K or parts of exchangeable K (0.01 M CaCl₂, 0.5 M NaHCO₃, 1 M NH₄oAc, or ammonium acetate lactate) was significantly (p < 0.05) related to the K yield only in the 1st yr after soil sampling. Potassium extracted with boiling in 1 M or 2 M HNO₃ was significantly related to the K yield only in the 2nd and 3rd yr. Potassium extracted with cold 2 M HCl, boiling 0.1 M HNO₃ or 0.5 M HNO₃ was significantly related to the K yield in all 3 yr after soil sampling. Among these extractants, 0.1 M and 0.5 M HNO₃‐extractable K were better predictors of K uptake than 2 M HCl‐extractable K. These three extractants release some non‐exchangeable K in addition to exchangeable K. The fraction of 1 M HNO₃‐K extractable with 0.1 M HNO₃ varied from 4% to 45%, whereas from 15% to 78% of 1 M HNO₃‐K was extractable with 0.5 M HNO₃. Consequently, the more easily releasable fraction of K extracted by boiling with 1 M HNO₃ varied considerably between different sites.     

中国小麦土壤速效钾丰缺指标与适宜施钾量研究

系统总结我国开展的小麦土壤速效钾丰缺指标与适宜施钾量研究,结果表明:30a来我国小麦土壤速效钾丰缺指标明显提高;不同区域之间小麦土壤速效钾丰缺指标差异颇大,以缺钾处理相对产量90%指标为例,土壤NH4OAc-K含量变动于80～246 mg/kg;除黄淮海平原、四川盆地、关中灌区和河套灌区外,我国小麦土壤速效钾丰缺指标研究存在很多空白区域;小麦土壤缺钾较为普遍,第2～4级为土壤速效钾集中分布的丰缺级别,缺钾处理相对产量大多处在70%～100%;土壤养分丰缺指标研究的试验点数不宜过少,丰缺指标高端和低端采用外推数据需谨慎,并应予以注明;适宜施钾量与土壤速效钾丰缺级别线性负相关,与小麦目标产量线性正相关,与钾肥当季利用率线性负相关;当钾肥当季利用率50%、目标产量3.0～12 t/hm2时,土壤速效钾丰缺级别第1～7级的小麦适宜施钾量范围依次为0、17～67、34～134、50～202、67～269、84～336和101～403 kg/hm2。     

Quantification and potential availability of non-symbiotically fixed 15N in soil

Summary Non-symbiotic N₂ fixation was studied under laboratory conditions in two soils from Pakistan (Hafizabad silt loam and Khurrarianwala silt loam) and one from Illinois, USA (Drummer silty clay loam) incubated in a ¹⁵N-enriched atmosphere. N₂ fixation was greatest with the Drummer soil (18–122 g g^–1 soil, depending upon the soil treatment) and lowest with the Khurrarianwala soil (4–81 g g^–1 soil). Fixation was increased by the addition of glucose, a close correlation being observed between the amount of glucose added and the amount of N₂ fixed in the three soils (r = 0.96). Efficiency of N₂ fixation varied with soil type and treatment and was greatest in the presence of added inorganic P. Application of Mo apparently had a negative effect on the amount and efficiency of N₂ fixation in all the soils. The percentage of non-symbiotically fixed ¹⁵N in potentially mineralizable form (NH ₄ ⁺ -N released in soil after a 15-day incubation period under anaerobic conditions) was low (2%–18%, depending upon the soil treatment), although most of the fixed N (up to 90%) was recovered as forms hydrolysable with 6N HCl. Recovery in hydrolysable forms was much greater for the fixed N than for the native soil N, indicating that the former was more available for uptake by plants.     

Changes in potassium availability and other soil properties due to soil ingestion by earthworms

An incubation experiment was conducted to study the changes that occur in potassium availability and other soil properties with ingestion of soil by earthworms. Two soils were used. Raumai soil with high non-exchangeable K and Milson soil with low non-exchangeable K were incubated with two species of earthworm, Aporrectodea caliginosa and Lumbricus rubellus, for 8 weeks. The casts and soil samples were analysed for exchangeable K, Ca, Mg, Na, and H, pH, organic C, and texture. The results indicated that in Raumai soil, the exchangeable K levels of the casts of both earthworm species were significantly higher than for the control soil, the effect being more marked for L. rubellus than for A. caliginosa. In Milson soil, the exchangeable K levels were significantly lower in the casts of both types of earthworm than in the control soil. The nitric acid-extractable K of the soil and casts was not markedly different for either soil type, but available non-exchangeable K values were significantly higher for the casts of L. rubellus from Milson soil than for the noningested Milson soil. In Raumai soil, the exchangeable Ca was higher in the casts of L. rubellus, exchangeable Mg and H were reduced, and exchangeable Na did not change markedly in the cast compared to the control soil. For Milson soil, the casts contained lower exchangeable Ca and H but higher Na and Mg than the control. The casts of both species of earthworm had significantly higher pH values for both soil types. There was no marked difference in the organic C content of the control soil and cast samples for Milson but a reduction in the casts of A. caliginosa for the Raumai soil. Finer fractions increased in the casts of both earthworm species in both soil types.     

Conductimetric determination of soil urease activity

Abstract

A fast and sensitive method to determine urease activity in soils is described. It involves extraction of NH₄‐N with 1 N. KC1 : 0.01 N HC1 and measurement of NH₄ concentration by electroconductivity using a steady state flow system across a membrane. Sampling was done directly from the extracts with an automatic sampler at 40 samples per hour. The detection limit for NH₄‐N was below 0.05 ppm in the extract. Extracts could be stored at room temperature for 17 hours before measuring NH₄. No post‐treatment hydrolysis of urea occured.