Cade-Menun Barbara J, Elkin Kyle R, Liu Corey W, Bryant Ray B, Kleinman Peter J A, Moore Philip A
Swift Current Research and Development Centre, Agriculture and Agri-Food Canada, Box 1030, Gate 4, Airport Drive, Swift Current, SK, S9H 3X2, Canada.
Pasture Systems and Watershed Management Research Unit, USDA-ARS, University Park, PA, 16802, USA.
Geochem Trans. 2018 Feb 21;19(1):7. doi: 10.1186/s12932-018-0052-9.
Phosphorus (P) can limit crop production in many soils, and soil testing is used to guide fertilizer recommendations. The Mehlich III (M3) soil test is widely used in North America, followed by colorimetric analysis for P, or by inductively coupled plasma-based spectrometry (ICP) for P and cations. However, differences have been observed in M3 P concentrations measured by these methods. Using P nuclear magnetic resonance (P-NMR) and mass spectrometry (MS), we characterized P forms in M3 extracts. In addition to the orthophosphate that would be detected during colorimetric analysis, several organic P forms were present in M3 extracts that would be unreactive colorimetrically but measured by ICP (molybdate unreactive P, MUP). Extraction of these P forms by M3 was confirmed by P-NMR and MS in NaOH-ethylenediaminetetraacetic acid extracts of whole soils and residues after M3 extraction. The most abundant P form in M3 extracts was myo-inositol hexaphosphate (myo-IHP, phytate), a compound that may not contribute to plant-available P if tightly sorbed in soil. Concentrations of myo-IHP and other organic P forms varied among soils, and even among treatment plots on the same soil. Extraction of myo-IHP in M3 appeared to be linked to cations, with substantially more myo-IHP extracted from soils fertilized with alum-treated poultry litter than untreated litter. These results suggest that ICP analysis may substantially over-estimate plant-available P in samples with high MUP concentrations, but there is no way at present to determine MUP concentrations without analysis by both colorimetry and ICP. This study also tested procedures that will improve future soil P-NMR studies, such as treatment of acid extracts, and demonstrated that techniques such as P-NMR and MS are complimentary, each yielding additional information that analysis by a single technique may not provide.
磷(P)会限制许多土壤中的作物产量,土壤测试用于指导肥料推荐。梅利希三号(M3)土壤测试在北美广泛使用,随后进行磷的比色分析,或对磷和阳离子进行基于电感耦合等离子体的光谱分析(ICP)。然而,通过这些方法测得的M3磷浓度存在差异。我们利用磷核磁共振(P-NMR)和质谱(MS)对M3提取物中的磷形态进行了表征。除了比色分析中会检测到的正磷酸盐外,M3提取物中还存在几种有机磷形态,它们在比色法中无反应,但可通过ICP测定(钼酸盐无反应磷,MUP)。通过P-NMR和MS在M3提取后的全土和残渣的氢氧化钠-乙二胺四乙酸提取物中证实了M3对这些磷形态的提取。M3提取物中最丰富的磷形态是肌醇六磷酸(肌醇六磷酸,植酸),如果该化合物在土壤中被紧密吸附,则可能对植物有效磷没有贡献。肌醇六磷酸和其他有机磷形态的浓度在不同土壤之间甚至同一土壤的不同处理地块之间都有所不同。M3中肌醇六磷酸的提取似乎与阳离子有关,从用明矾处理过的家禽粪便施肥的土壤中提取的肌醇六磷酸比未处理的粪便要多得多。这些结果表明,对于MUP浓度高的样品,ICP分析可能会大幅高估植物有效磷,但目前没有办法在不通过比色法和ICP分析的情况下确定MUP浓度。本研究还测试了可改进未来土壤P-NMR研究的程序,如酸提取物的处理,并证明了P-NMR和MS等技术是互补的,每种技术都能提供单一技术分析可能无法提供的额外信息。