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N analyser

Manufactured by Leco
Sourced in United States

The N-analyser is a laboratory instrument designed to determine the nitrogen content in a wide range of sample types. It employs a combustion method to measure the total nitrogen concentration accurately and precisely.

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4 protocols using n analyser

1

Leaf Nutrient Extraction and Analysis

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Leaf samples were analyzed for macro and micro at Bemlab (Pty) Ltd. (Somerset West, Cape Town, South Africa), a commercial laboratory. Leaves were washed with Teepol solution, rinsed with de-ionised water, and dried at 70 °C overnight in an oven. The dried leaves were then milled and ashed at 480 °C, and shaken up in a 50:50 HCl (50%) solution for extraction through filter paper [52 ,53 ]. The potassium (K), phosphorus (P), Ca, Mg, sodium (Na), manganese (Mn), iron (Fe), copper (Cu), zinc (Z), and boron (B) contents of the extracts were analyzed using the Ash method. The total nitrogen (N) content of the leaves was determined through total combustion in a Leco N-analyser. The amounts of N, P, K, Ca, and Mg were converted from percentage (%) to mg/kg. 10,000 was used as the conversion factor.
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2

Analyzing Leaf Nutrient Composition

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Leaf samples were analyzed for macronutrients and micronutrients by a commercial laboratory, Bemlab Pty Ltd, Somerset West, South Africa. Leaves were washed with a teepol solution, rinsed with de-ionized water and dried at 70 °C overnight in the thermo-oven. The dried leaves were then milled and ashed at 480 °C and shaken up in a 50:50 Hydrochloric (HCl) (50%) solution for extraction through filter paper (Campell and Plank, 1998 ; Miller, 1998 ). Potassium (K), Phosphorus (P), Calcium (Ca), Magnesium (Mg), Sodium (Na), Manganese (Mn), Iron (Fe), Copper (Cu), Zinc (Z) and Boron (B) contents of the extracts were analysed using the Ash method. Total Nitrogen (N) content of the leaves was determined through total combustion in a Leco N-analyser. The amount of N, P, K, Ca and Mg were converted from percentage (%) to mg gDW−1, while Mn, Fe, Cu, Z and B were converted from percentage (%) to μg gDW−1
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3

Elemental Profiling of Plant Bulbs

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Bulbs of randomly selected plants from each treatment were analysed for macro-element and micro-element contents using an inductively coupled mass spectrometry (ICP-MS) and a LECO-nitrogen analyser with appropriate standards (Bemlab (PTY) Ltd., Somerset West, South Africa). Each treatment had three replicates. Briefly, the bulbs were cleaned in a Teepol solution, rinsed with deionised water, and dried in an oven at 70 °C overnight. Thereafter, the dried bulbs were pulverised, ashed at 480 °C, and agitated in a 50:50 HCl (50%) solution for extraction through filter paper [29 ], and then used to determine the potassium (K), phosphorus (P), calcium (Ca), magnesium (Mg), sodium (Na), manganese (Mn), iron (Fe), copper (Cu), zinc (Z), and boron (B) content of the extracts. Total combustion in a Leco N-analyser was used to assess the bulbs’ total nitrogen (N) contents. N, P, K, Ca, and Mg values were converted from percentages to mg/kg using a conversion factor of 10,000 [30 ].
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4

Feed Composition Analysis Protocol

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Experimental diets were ground to pass through a 1 mm screen before chemical analysis. Feed samples were analyzed for dry matter, crude protein, gross energy, Ca and P. Dry matter content was determined according to the AOAC (1990) by oven drying 5 g of sample at 102 °C overnight. Gross energy was measured using an adiabatic bomb calorimeter (model 6400, Parr Instrument, Moline, IL, USA) which had been calibrated using benzoic acid as a standard. Nitrogen content was determined by the combustion method (AOAC, 2005 ) using the LECO N analyser (model CNS-2000; LECO Corp., St. Joseph, MI, USA) and crude protein was calculated as nitrogen × 6.25. Samples for analysis of Ca and P were ashed for 12 h and digested according to AOAC (2005) and read on a Varian inductively coupled plasma mass spectrometer (Varian Inc., Palo Alto, CA, USA).
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