Pacific Ocean saturation profile

Saturation profiles for the northern Atlantic and Pacific oceans, and the central Indian Ocean (GEOSECS stations 31,221,450). 

Vertical concentration profiles of (a) temperature, (b) potential density, (c) salinity, (d) O2, (e) % saturation of O2, (f) bicarbonate and TDIC, (g) carbonate alkalinity and total alkalinity, (h) pH, (i) carbonate, ( ) carbon dioxide and carbonic acid concentrations, and (k) carbonate-to-bicarbonate ion concentration ratio. Curves labeled f,p have been corrected for the effects of in-situ temperature and pressure on equilibrium speciation. Curves labeled t, 1 atm have been corrected for the in-situ temperature effect, but not for that caused by pressure. Data from 50°27.5 N, 176°13.8 W in the North Pacific Ocean on June 1966. Source From Culberson, C., and R. M. Pytkowicz (1968). Limnology and Oceanography, 13, 403-417. 

Typical vertical saturation profiles for the North Atlantic, North Pacific, and Central Indian oceans are presented in Figure 4.10. The profiles in the Atlantic and Indian oceans are similar in shape, but Indian Ocean waters at these GEOSECS sites are definitely more undersaturated than the Atlantic Ocean. The saturation profile in the Pacific Ocean is complex. The water column between 1 and 4 km depth is close to equilibrium with calcite. This finding is primarily the result of a broad oxygen minimum-C02 maximum in mid-water and makes choosing the saturation depth (SD) where Oc = 1 difficult (the saturation depth is also often referred to as the saturation level SL). 

The Geochemical Ocean Section Program (GEOSECS) has produced data from which it is possible to profile the saturation state of seawater with respect to calcite and aragonite in the Atlantic and Pacific oceans. Representative north-south calcite saturation profiles for the Western Atlantic and Central Pacific oceans are presented in Figures 5 and 6 (based on 39). It was observed that the saturation state of seawater with respect to calcite at the CCD was close to constant ( 2 = 0.70 I" 0,05) except in the southern extremes (39). Broecker and Takahashi (31) have recently found that the carbonate ion concentration is close to constant at the FL, when appropriate corrections are made for pressure. The saturation state of seawater at the FL, calculated by the method presented in this paper, is 0.80 0.05. Berger (40) has presented profiles for Rq, FL, CCD and CSL (calcite saturation level) in the eastern and western Atlantic ocean (see... 

Figure 3 Bathymetric profiles of calcium carbonate (calcite) saturation for hydrographic stations in the Atlantic and Pacific Oceans (data from Takahashi etai 1980). Carbonate saturation here is expressed as ACOa ", defined as the difference between the in situ carbonate ion concentration and the saturation carbonate ion concentration at each depth ACOa " = [C03 ]seawater - [COa Jsaturation)-The saturation horizon corresponds to the transition from waters oversaturated to waters undersaturated with respect to calcite (A 003 = 0). This level is deeper in the Atlantic than in the Pacific because Pacific waters are COa-enriched and [C03 ]-depleted as a result of thermohaline circulation patterns and their longer isolation from the surface. The Atlantic data are from GEOSECS Station 59 (30°12 S, 39°18 W) Pacific data come from GEOSECS Station 235 (16°45 N,161°23 W).

Saturation state of seawater, Cl, with respeot to (a) calcite and (b) aragonite as a function of depth. The dashed vertical line marks the saturation horizon. North Pacific profile is from 27.5°N 179.0°E (July 1993) and North Atlantio profile is from 24.5°N 66.0°W (August 1982) from CDIAC/WOCE database http //cdiac.esd.oml.gov/oceans/CDIACmap.html) Section P14N, Stn 70 and Section A05, Stn 84. Source From Zeebe, R.E. and D. Wolf-Gladrow (2001) Elsevier Oceanography Series, 65, Elsevier, p. 26. 

Figure 11 Depth profiles of (a) N2O concentration and (b) and (c) <5 0 of N2O at station ALOHA in the subtropical North Pacific (22° 45 N, 158° W) during four separate cruises. The solid line in (a) indicates theoretical saturation with atmospheric N2O at in situ temperatures and salinities. The minima in and <5 0 around 200 m are thought to be due to significant in situ production of N2O from nitrification. The broad isotopic maxima at depth are likely due to N2O consumption, perhaps in the denitrifying waters along the eastern Pacific margin. The filled squares at the top of (b) and (c) represent measurements of <5 N and <5 0 of atmospheric N2O during the Hawaii Ocean Time-series 76 cruise, and arrows indicate the range of historical measurements as of the late 1980s. Reprinted from Dore JE, Popp BN, Karl DM, and Sansone FJ (1998) A large source of atmospheric nitrous oxide from subtropical North Pacific surface waters. Nature 396 63-66.

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