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To reduce the carbon-to-nitrogen (C:N) ratio, pine tree substrate (PTS) and other wood-based substrates can be precharged with urea so that growers do not have to add extra nitrogen (N) during crop production to compensate for immobilization. However, the impact of urea hydrolysis from this addition on the substrate solution has not been documented for wood-based substrates. The objectives of these experiments were to determine how urea hydrolysis in PTS impacts substrate solution and how hydrolysis is affected by urea and lime rates. In Expt. 1, 16-month-old pine chips (from loblolly pine trees, Pinus taeda L.) were milled to make PTS and PTS was amended with 0 or 1.0 kg·m−3 dolomitic limestone in factorial combination with urea-N rates of 0, 0.5, 1.0, 1.5, or 2.0 mg·g−1 dry weight. Urea hydrolysis was quantified by the detection of NH4-N in the substrate solution at 0, 48, 96, and 144 hours after urea addition. Substrate pH and electrical conductivity (EC) values were also measured. In Expt. 2, non-limed PTS was treated with the same urea rates as described; NH4-N and pH were measured at 24 and 48 hours after urea addition. Substrate solutions were incubated with jackbean urease to determine the remaining urea-N amount after 144 hours in Expt. 1 and after 24 and 48 hours in Expt. 2. In Expt. 1, NH4-N increased from 0 to 48 hours for the 0 and 1.0-kg·m−3 lime treatments and for all urea-N rates (except for the 0 rate); NH4-N did not increase thereafter. As urea-N rate increased, the amount of NH4-N increased and more N was detected for the limed PTS than in the non-limed PTS. Initial substrate pH values for the 0 and 1.0-kg·m−3 lime treatments were 4.5 and 5.6, respectively, and peaked 48 hours after urea application; pH values were higher in the limed PTS than for the non-limed PTS. At the highest urea-N rate and after 48 hours (Expt. 1), the PTS pH value increased 3.1 units to 7.6 for the non-limed PTS and the value increased 2.3 units to 7.9 for limed PTS. In Expt. 2 the increase in PTS pH values was approximately half of the Expt. 1 pH increases. Samples treated with urease derived from jackbean had less than 2% of the initial urea amount after 144 hours in Expt. 1 and after 48 hours in Expt. 2. However, less than 13% of the total amount of urea-N added to PTS was detected as NH4-N in the non-limed treatment after 144 hours in Expt. 1 (for all urea rates); detected amounts for the 1.0-kg·m−3 lime treatment ranged from 15.5% to 18.3%. Five percent or less of the total amount of urea-N added to PTS was detected as NH4-N in non-limed PTS after 48 hours in Expt. 2 (for all urea rates). The large amount of unrecovered NH4-N is likely explained by microbial N consumption. Using pH increase as an indication of urea hydrolysis, we found that an initial pH of 4.5 or higher (Expt. 1) resulted in twice the urea hydrolysis as an initial pH of 4.2 (Expt. 2). Initial substrate pH had a major impact on the amount of pH increase and substrate pH status and our findings suggest that the urea precharge rate should be based on the initial pH of the substrate.
Pine tree substrate (PTS), for container plant production, is a relatively new alternative to the commonly used pine bark and peat substrates. Fertility management requires knowledge of nitrogen transformations in this new substrate. The objective of this study was to document the occurrence of nitrification in PTS and to determine if nitrification and density of nitrifying microorganisms are affected by substrate storage time and lime and peat amendments. Pine tree substrate was manufactured by hammermilling chips of ≈15-year-old loblolly pine trees (Pinus taeda L.) through two screen sizes, 4.76 mm (PTS) and 15.9 mm amended with peat (3PTS:1 peat, v:v, PTSP). Pine tree substrate and PTSP were amended with lime at five rates and a peat–perlite mix (4 peat:1 perlite, v:v, PL) served as a control treatment for a total of 11 treatments. Substrates were prepared, placed in plastic storage bags, and stored on shelves in an open shed in Blacksburg, VA. Subsamples were taken at 1, 42, 84, 168, 270, and 365 days after storage. At each subsampling day, each substrate was placed into 12 1-L containers. Six of the 12 were left fallow and six were planted with 14-day-old marigold (Tagetes erecta L. ‘Inca Gold’) seedlings; all containers were placed on a greenhouse bench. Substrates were also collected for most probable number (MPN) assays for nitrifying microorganism quantification. Substrate solution pH, electrical conductivity (EC), ammonium-N (NH4-N), and nitrate-N (NO3-N) were measured on fallow treatments. Marigold substrate solution pH, EC, NH4-N, and NO3-N were measured after 3 weeks of marigold growth. Nitrate-N was detected in fallow containers at low concentrations (0.4 to 5.4 mg·L−1) in PTS in all limed treatments at all subsampling days, but in the non-limed treatment, only at Days 270 and 365. Nitrate-N was detected in the fallow containers at low concentrations (0.7 to 13.7 mg·L−1) in PTSP in the 4- and 6-kg·m−3 lime rates at all subsampling days. Nitrite-oxidizing microorganisms were present in PTS at all subsampling days with the highest numbers measured at Day 1. Ammonium-to-nitrate ratios for the marigold substrate solution extracts for both PTS and PTSP decreased as pH increased. This study shows that nitrifying microorganisms are present and nitrification occurs in PTS and PTSP and is positively correlated to substrate pH.
Pine tree substrate (PTS) is a relatively new alternative to the commonly used pine bark and peat-based substrates for container crop production. Physical and chemical properties of freshly manufactured PTS have been studied; however, this new substrate will sometimes be manufactured and stored for later use by growers. The objective of this research was to determine how chemical and physical properties of PTS were affected by storage duration with or without amendments of limestone or peatmoss. We also studied how the growth of marigold was influenced by PTS storage time and by lime and peat amendments. Substrate properties studied were pH, cation exchange capacity (CEC), electrical conductivity (EC), carbon-to-nitrogen ratio (C:N), bulk density (BD), and particle size distribution. Pine tree substrate was manufactured by hammermilling chips of ≈15-year-old loblolly pine trees (Pinus taeda L.) through two screen sizes, 4.76 mm (PTS) and 15.9 mm [amended with peat (PTSP)]. Pine tree substrate and PTSP were amended with lime at five rates and a peat–perlite mix (PL) served as a control treatment. Substrates were prepared, placed in plastic storage bags, and stored on shelves in an open shed in Blacksburg, VA. Substrates were subsampled at 1, 42, 84, 168, 270, and 365 days after storage. At each subsampling day, twelve 1-L containers were filled with a subsample of each treatment. Six of the 12 were left fallow and six were planted with 14-day-old marigold (Tagetes erecta L. ‘Inca Gold’) seedlings. Substrate was also collected for analysis of CEC, C:N, BD, and particle size distribution. The pH of non-limed PTS decreased during storage, and at least 1 kg·m−3 lime was needed to maintain PTS pH 5.4 or greater over the 365-day storage period (Day 1 pH = 5.8) and 2 to 4 kg·m−3 was needed to maintain PTSP pH 5.4 or greater for 365 days (Day 1 pH = 5.2). EC measurements were highest at Day 1 (1.02 to 1.21 dS·m−1) in all treatments and decreased by Day 42. Cation exchange capacity decreased over time in non-limed PTS and PTSP. Carbon-to-nitrogen ratio and BD remained the same over time for all treatments. There were minor changes in particle size distribution for limed PTS. Marigold growth in all limed PTS and PTSP treatments was equal to or greater than in PL, except at Day 1; the lower growth in PTS and PTSP at Day 1 compared with PL suggests that freshly manufactured PTS may contain a phytotoxic substance that was not present in PTS by Day 42. Pine tree substrate and PTSP are relatively stable when stored as described previously, except for a pH decrease that can be prevented with additions of lime before storage.