iainwilliams
Contributor
Hello
I would like someone with more knowledge on this topic subject to make a comment.
I have been reading with interest a number of articles regarding reverse profiles and profiles that do not correspond to diving the deepest depth first, followed by a progressively shallower depth.
SCENARIO: If we are diving below 10 m (less than 10 m is where the greatest pressure change occurs) and alter our depths during the dive saw tailing to a shallower then deeper depth, but not going outside a 10-15 m depth envelope. Then surely a computer (ie UWATEC) should be able to accurately track the N2 within your tissue compartments at the various depths (I know this what a computer does).
The different depths cause N2 to diffuse into different theoretical compartments. The shallow portion of the dive will cause N2 to accumulate in slow to medium tissues whilst the deeper dive portion will cause N2 to diffuse into faster tissues. As the depth is below 10 m and outside the greatest pressure change, and provided ascent rates and bottom times were kept in order, micro bubbling would not occur.
Therefore, altering your depth (deep, shallow then deep again) should be OK. Likewise, if we did a shallow dive in the morning (ie 15 M) and a deeper dive in the afternoon (ie 20m), then this should also be OK provided we used a computer to track N2.
Does anyone have any thoughts on this controversial issue which is the oppsoit to what all divers have been taught? Thanks Iain
I would like someone with more knowledge on this topic subject to make a comment.
I have been reading with interest a number of articles regarding reverse profiles and profiles that do not correspond to diving the deepest depth first, followed by a progressively shallower depth.
SCENARIO: If we are diving below 10 m (less than 10 m is where the greatest pressure change occurs) and alter our depths during the dive saw tailing to a shallower then deeper depth, but not going outside a 10-15 m depth envelope. Then surely a computer (ie UWATEC) should be able to accurately track the N2 within your tissue compartments at the various depths (I know this what a computer does).
The different depths cause N2 to diffuse into different theoretical compartments. The shallow portion of the dive will cause N2 to accumulate in slow to medium tissues whilst the deeper dive portion will cause N2 to diffuse into faster tissues. As the depth is below 10 m and outside the greatest pressure change, and provided ascent rates and bottom times were kept in order, micro bubbling would not occur.
Therefore, altering your depth (deep, shallow then deep again) should be OK. Likewise, if we did a shallow dive in the morning (ie 15 M) and a deeper dive in the afternoon (ie 20m), then this should also be OK provided we used a computer to track N2.
Does anyone have any thoughts on this controversial issue which is the oppsoit to what all divers have been taught? Thanks Iain