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| title | chunk | source | category | tags | date_saved | instance |
|---|---|---|---|---|---|---|
| Decompression theory | 7/17 | https://en.wikipedia.org/wiki/Decompression_theory | reference | science, encyclopedia | 2026-05-05T10:06:49.112339+00:00 | kb-cron |
=== Tissue compartments === One attempt at a solution was the development of multi-tissue models, which assumed that different parts of the body absorbed and eliminated gas at different rates. These are hypothetical tissues which are designated as fast and slow to describe the rate of saturation. Each tissue, or compartment, has a different half-life. Real tissues will also take more or less time to saturate, but the models do not need to use actual tissue values to produce a useful result. Models with from one to 16 tissue compartments have been used to generate decompression tables, and dive computers have used up to 20 compartments. For example: Tissues with a high lipid content can take up a larger amount of nitrogen, but often have a poor blood supply. These will take longer to reach equilibrium, and are described as slow, compared to tissues with a good blood supply and less capacity for dissolved gas, which are described as fast. Fast tissues absorb gas relatively quickly, but will generally release it quickly during ascent. A fast tissue may become saturated in the course of a normal recreational dive, while a slow tissue may have absorbed only a small part of its potential gas capacity. By calculating the levels in each compartment separately, researchers are able to construct more effective algorithms. In addition, each compartment may be able to tolerate more or less supersaturation than others. The final form is a complicated model, but one that allows for the construction of algorithms and tables suited to a wide variety of diving. A typical dive computer has an 8–12 tissue model, with half times varying from 5 minutes to 400 minutes. The Bühlmann tables use an algorithm with 16 tissues, with half times varying from 4 minutes to 640 minutes. Tissues may be assumed to be in series, where dissolved gas must diffuse through one tissue to reach the next, which has different solubility properties, in parallel, where diffusion into and out of each tissue is considered to be independent of the others, and as combinations of series and parallel tissues, which becomes computationally complex.
=== Ingassing model === The half time of a tissue is the time it takes for the tissue to take up or release 50% of the difference in dissolved gas capacity at a changed partial pressure. For each consecutive half time the tissue will take up or release half again of the cumulative difference in the sequence ½, ¾, 7/8, 15/16, 31/32, 63/64 etc. Tissue compartment half times range from 1 minute to at least 720 minutes. A specific tissue compartment will have different half times for gases with different solubilities and diffusion rates. Ingassing is generally modeled as following a simple inverse exponential equation where saturation is assumed after approximately four (93.75%) to six (98.44%) half-times depending on the decompression model. There is normally no phase change during ingassing after the gases are dissolved in the blood of the pulmonary circulation in the lungs. They remain in solution in whichever tissues they reach by perfusion and diffusion, so the model is fairly robust. The exception is for isobaric counterdiffusion which can induce bubble growth and possibly bubble formation when a gas of different solubility is introduced to the breathing mixture. This model may not adequately describe the dynamics of outgassing if gas phase bubbles are present.
=== Outgassing models === For optimised decompression the driving force for tissue desaturation should be kept at a maximum, provided that this does not cause symptomatic tissue injury due to bubble formation and growth (symptomatic decompression sickness), or produce a condition where diffusion is retarded for any reason. There are two fundamentally different ways this has been approached. The first is based on an assumption that there is a level of supersaturation which does not produce symptomatic bubble formation and is based on empirical observations of the maximum decompression rate which does not result in an unacceptable rate of symptoms. This approach seeks to maximise the concentration gradient providing there are no symptoms, and commonly uses a slightly modified exponential half-time model. The second assumes that bubbles will form at any level of supersaturation where the total gas tension in the tissue is greater than the ambient pressure and that gas in bubbles is eliminated more slowly than dissolved gas. These philosophies result in differing characteristics of the decompression profiles derived for the two models: The critical supersaturation approach gives relatively rapid initial ascents, which maximize the concentration gradient, and long shallow stops, while the bubble models require slower ascents, with deeper first stops, but may have shorter shallow stops. This approach uses a variety of models.