Abstract

A laboratory experiment evaluated the rate of urea hydrolysis and ammonia volatilization from urea (U) mixed in organo‐mineral (O‐M) fertilizers. These fertilizers were incubated in soil in the presence or absence of N‐(n‐butyl)thiophosphoric triamide (NBPT) as a urease inhibitor. Two organic matrices, leather (L) and peat (P), were used to prepare the O‐M fertilizers. In the absence of NBPT, the highest ammonia losses and the fastest rate of urea hydrolysis were in the soil treated with the fertilizer containing leather (UL50). Significantly lower ammonia losses occurred with peat‐based fertilizers. Although the fertilizer containing peat (UP50) stimulated the rate of urea hydrolysis with respect to the urea alone, no increase in ammonia volatilization was detected. NBPT‐containing fertilizers were stored for different times (0,7, 30, and 60 days) and temperatures (25°C and 40°C), and the NBPT recovery was monitored by extraction and analysis by HPLC. The NBPT recovery decreased by increasing either the storage time or the storage temperature. Differences among the fertilizers occurred after storage at 40°C for 30 or 60 days. With UN, in spite of about 25% extracted amount of NBPT, the ammonia losses did not increase with respect to the non‐stored fertilizer. On the contrary, no inhibitor was recovered from either of the O‐M fertilizers (UNL and UNP). However, in the presence of leather, NBPT reduced the volatilization losses by 35 to 40%, whereas in the presence of peat, a complete loss of NBPT efficiency occurred. In general, either the inhibitor recovery or efficiency were affected by the storage conditions or the type of organic matrix.

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