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Comparing with the existing bubble pressure test method, the specimen is initially placed vertically with a given liquid and air on each side.
The influence of scattering and propagation of electrons within the specimen is initially discussed separately and then treated in terms of a two-state channeling theory.
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Each specimen was initially made out by cutting off horizontally in the medium of the adjacent vertebra.
The specimen was initially homogenised, using a rotary star homogeniser then underwent further homogenisation using a Q1A shredder (Qiagen® Ltd, West Sussex UK).
There, the organism was identified as B. melitensis 18 days after the specimen was initially obtained and 10 days after it was sent to the reference laboratory.
Three sections from each specimen were initially examined under light microscopy at low magnification (× 100), allowing the evaluation of surface area occupied by apoptotic cells.
To minimize axial damage to EOM fibers, each specimen was initially prepared in the shape of an approximately 7 mm long prism with a 4 mm × 2 mm cross-section.
G1: Each specimen was initially finished with a diamond point 2135 FF (KG Sorensen, Barueri, SP, Brazil), intermittently in one direction, with cooling and high speed (Kavo do Brasil Indústria e Comércio Ltda, Joinville, SC, Brazil), for 30 s (S1).
All the specimens were initially austenitized at 927°C (1700°F) for 2 h.
In order to evaluate the residual seismic capacity of CFRP-confined columns, three of the confined specimens were initially loaded to induce damage.
The specimens were initially fatigued at Δε=±0.2% or ±0.3% for 1×104 cycles and subsequently cyclically deformed after the change in Δε from ±0.2%to±0.3%3% or from ±0.3%to±0.2%2%.
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CEO of Professional Science Editing for Scientists @ prosciediting.com