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All samples were air-dried and sieved to pass through 2 mm mesh.
Equal amounts of soil from each of the 3 replicate mini-plots were then combined, mixed thoroughly and sieved (mesh-width 3 mm) to remove large particles.
Samples were sieved prior to testing to remove organic debris.
Soil was sieved to 2 mm to ensure homogeneity.
The sand was sieved and washed, and the fraction retained between sieves of 160 m and 425 m pore size was used.
Samples were sieved and sorted to separate plant debris from aphids.
The aphid suspension was sieved and sorted to remove plant debris.
Thereafter, they were washed and sieved through a 0.5 cm-wide mesh to retain the coarse fraction.
The air-dried samples were sieved through a 150-mesh.
Soils were dried, sieved and mixed within each category to create inocula.
Ferrallitic forest soil (top soil: 10-15 cm deep) was collected on the same site and sieved through a 1-cm screen.
The 1 kg samples of dung and manure were sieved coarsely (75 mm and 25 mm mesh) with water, to reduce sample bulk.
Soil was first sieved and large particulate organic matter was eliminated by hand.
The residue was rinsed and sieved again through a 10 m mesh.
Ants were baited with milled rice that was sieved into five particle sizes: < 0.2, 0.2-0.5, 0.5-0.8, 0.8-1.5 and 1.5-2.5 mm.