McDowell R W, Condron L M, Mahieu N, Brookes P C, Poulton P R, Sharpley A N
USDA-ARS Pasture Systems and Watershed Management Research Laboratory, University Park, PA 16802-3702, USA.
J Environ Qual. 2002 Mar-Apr;31(2):450-6.
In many intensive agroecosystems continued inputs of phosphorus (P) over many years can significantly increase soil P concentrations and the risk of P loss to surface waters. For this study we used solid-state 31P nuclear magnetic resonance (NMR) spectroscopy, high-power decoupling with magic angle spinning (HPDec-MAS) NMR, and cross polarization with magic angle spinning (CP-MAS) NMR to determine the chemical nature of potentially mobile P associated with aluminum (Al) and calcium (Ca) in selected arable soils. Three soils with a range of bicarbonate-extractable Olsen P concentrations (40-102 mg P kg(-1)) were obtained from a long-term field experiment on continuous root crops at Rothamsted, UK, established in 1843 (sampled 1958). This soil has a threshold or change point at 59 mg Olsen P kg(-1), above which potentially mobile P (as determined by extraction with water or 0.01 M CaCl2) increases much more per unit increase in Olsen P than below this point. Results showed that CaCl2 and water preferentially extracted Al-P and Ca-P forms, respectively, from the soils. Comparison among the different soils also indicated that potentially mobile P above the threshold was largely present as a combination of soluble and loosely adsorbed (protonated-cross polarized) P forms largely associated with Ca, such as monetite (CaHPO4) and dicalcium phosphate dihydrate (CaHPO4-2H2O), and some Al-associated P as wavellite. The findings of this study demonstrate that solid-state NMR has the potential to provide accurate information on the chemical nature of soil P species and their potential mobility.
在许多集约化农业生态系统中,多年来持续投入磷(P)会显著增加土壤磷浓度以及磷流失到地表水的风险。在本研究中,我们使用固态³¹P核磁共振(NMR)光谱、魔角旋转高功率去耦(HPDec-MAS)NMR和魔角旋转交叉极化(CP-MAS)NMR来确定选定耕地土壤中与铝(Al)和钙(Ca)相关的潜在可移动磷的化学性质。从英国洛桑试验站1843年建立的长期连续种植块根作物田间试验中获取了三种土壤,其碳酸氢盐提取的 Olsen 磷浓度范围为40 - 102 mg P kg⁻¹(于1958年采样)。这种土壤在59 mg Olsen P kg⁻¹处有一个阈值或变化点,高于此点时,每单位 Olsen 磷增加量中潜在可移动磷(通过水或0.01 M CaCl₂提取测定)的增加幅度比低于此点时大得多。结果表明,CaCl₂和水分别优先从土壤中提取Al - P和Ca - P形态。不同土壤之间的比较还表明,高于阈值的潜在可移动磷主要以可溶和松散吸附(质子化交叉极化)的磷形态存在,这些形态主要与Ca相关,如磷酸一钙(CaHPO₄)和磷酸二钙二水合物(CaHPO₄·2H₂O),以及一些与Al相关的磷如磷铝石。本研究结果表明,固态NMR有潜力提供有关土壤磷形态的化学性质及其潜在移动性的准确信息。