Salinity

Measurement and definition difficulties arise because natural waters contain a complex mixture of many different elements from different sources (not all from dissolved salts) in different molecular forms. The chemical properties of some of these forms depend on temperature and pressure. Many of these forms are difficult to measure with high accuracy, and in any case complete chemical analysis is not practical when analyzing multiple samples. Different practical definitions of salinity result from different attempts to account for these problems, to different levels of precision, while still remaining reasonably easy to use.

For practical reasons salinity is usually related to the sum of masses of a subset of these dissolved chemical constituents (so-called solution salinity), rather than to the unknown mass of salts that gave rise to this composition (an exception is when artificial seawater is created). For many purposes this sum can be limited to a set of eight major ions in natural waters,[7][8] although for seawater at highest precision an additional seven minor ions are also included.[6] The major ions dominate the inorganic composition of most (but by no means all) natural waters. Exceptions include some pit lakes and waters from some hydrothermal springs.

The concentrations of dissolved gases like oxygen and nitrogen are not usually included in descriptions of salinity.[2] However, carbon dioxide gas, which when dissolved is partially converted into carbonates and bicarbonates, is often included. Silicon in the form of silicic acid, which usually appears as a neutral molecule in the pH range of most natural waters, may also be included for some purposes (e.g., when salinity/density relationships are being investigated).

The term 'salinity' is, for oceanographers, usually associated with one of a set of specific measurement techniques. As the dominant techniques evolve, so do different descriptions of salinity. Salinities were largely measured using titration-based techniques before the 1980s. Titration with silver nitrate could be used to determine the concentration of halide ions (mainly chlorine and bromine) to give a chlorinity. The chlorinity was then multiplied by a factor to account for all other constituents. The resulting 'Knudsen salinities' are expressed in units of parts per thousand (ppt or ‰).

The use of electrical conductivity measurements to estimate the ionic content of seawater led to the development of the scale called the practical salinity scale 1978 (PSS-78).[9][10] Salinities measured using PSS-78 do not have units. The suffix psu or PSU (denoting practical salinity unit) is sometimes added to PSS-78 measurement values.[11] The addition of PSU as a unit after the value is "formally incorrect and strongly discouraged".[2]

In 2010 a new standard for the properties of seawater called the thermodynamic equation of seawater 2010 (TEOS-10) was introduced, advocating absolute salinity as a replacement for practical salinity, and conservative temperature as a replacement for potential temperature.[6] This standard includes a new scale called the reference composition salinity scale. Absolute salinities on this scale are expressed as a mass fraction, in grams per kilogram of solution. Salinities on this scale are determined by combining electrical conductivity measurements with other information that can account for regional changes in the composition of seawater. They can also be determined by making direct density measurements.

A sample of seawater from most locations with a chlorinity of 19.37 ppt will have a Knudsen salinity of 35.00 ppt, a PSS-78 practical salinity of about 35.0, and a TEOS-10 absolute salinity of about 35.2 g/kg. The electrical conductivity of this water at a temperature of 15 °C is 42.9 mS/cm.[6][12]

On the global scale, it is extremely likely that human-caused climate change has contributed to observed surface and subsurface salinity changes since the 1950s, and projections of surface salinity changes throughout the 21st century indicate that fresh ocean regions will continue to get fresher and salty regions will continue to get saltier.[13]

Salinity is serving as a tracer of different masses. Surface water is pulled in to replace the sinking water, which in turn eventually becomes cold and salty enough to sink. Salinity distribution contributes to shape the oceanic circulation.

Limnologists and chemists often define salinity in terms of mass of salt per unit volume, expressed in units of mg/L or g/L.[7] It is implied, although often not stated, that this value applies accurately only at some reference temperature because solution volume varies with temperature. Values presented in this way are typically accurate to the order of 1%. Limnologists also use electrical conductivity, or "reference conductivity", as a proxy for salinity. This measurement may be corrected for temperature effects, and is usually expressed in units of μS/cm.

A river or lake water with a salinity of around 70 mg/L will typically have a specific conductivity at 25 °C of between 80 and 130 μS/cm. The actual ratio depends on the ions present.[14] The actual conductivity usually changes by about 2% per degree Celsius, so the measured conductivity at 5 °C might only be in the range of 50–80 μS/cm.

Direct density measurements are also used to estimate salinities, particularly in highly saline lakes.[4] Sometimes density at a specific temperature is used as a proxy for salinity. At other times an empirical salinity/density relationship developed for a particular body of water is used to estimate the salinity of samples from a measured density.