*********** +++++++++++++++++++++ 030696B.CHM + Source: ONR Asia + *********** +++++++++++++++++++++ Contributory Categories: BIO, PHY Country: Japan From: International Workshop on The Okhotsk Sea and Arctic The Physics and BioGeochemistry implied to the Global Cycles (Influence of Sea Ice on Climate and Marine Ecosystems) 29 Feb. - 1 March 1996, Tokyo, Japan KEYWORDS: Japan, Sea of Okhotsk; Isotopes, Tracers, Water Masses +++++ Items 1-3 this message, Items 4-5 next message Item 1 CHEMICAL OCEANOGRAPHY OF OKHOTSK SEA by C.S. Wong Ocean Biogeochemistry Institute of Ocean Sciences P.O.Box 6000, Sidney, B.C. Canada V8L 4B2 Chemical oceanography of Okhotsk Sea was studied by the Institute of Ocean Sciences in Sidney, B.C. Jointly with the Pacific Oceanological Institute in Vladivostok, Russ a, using the MV Nesmeyanov along WOCE Line PIW starting in the Pacific Ocean near Bussol' Strait in the Kuril Island, crossing the basin and shelf regions of the Okhotsk Sea and terminating near the city of Okhotsk on the Siberian shore, during the period August 30-September 21, 1993. Okhotsk Sea has two major basins: the shallower Deryugin Basin to a depth of about 1,500 m and the deeper Kuril Basin to 3,500 m. The blogeochemical and oceanographic processes are different in these basins. The Okhotsk Sea is a marginal sea bounded by land on three sides and the Kuril Island chain, separating it from the subarctic North Pacific, with connection to the salty Japan Sea through two shallow straits, the Soya Strait (40 m sill depth) and the Tartar Strait (100 m sill depth) and to the fresher North Pacific through two deep straits, the Bussol' Strait ( 2300 m sill depth) and the Kruzenshtema Strait (1900 m sill depth). The chemical properties of the Okhotsk Sea are affected by the water exchanges with the salty Japan Sea waters, the large gross exchange of 15 Sv with the North Pacific through the deep Straits, formation of the Okhotsk Sea shelf waters during winter ice formation and the mixing of inflowing North Pacific waters to produce the North Pacific Intermediate Waters (Wong et al., 1995). The physical oceanography of the WOCE Line PI W was described in Howard et al. (1995). For the 1993 WOCE sections in Okhotsk Sea, water samples and CTD casts were obtained using a General Oceanics Rosette with 10 L. Niskin PVC samplers. The measurements included temperature, salinity, dissolved oxygen, dissolved nutrients (phosphate, nitrate and silicate) and chlrofluorocarbons F- I I and F- 12 following procedures outlined in the WOCE protocol (WOCE, 1994). JGOFS Global C02 Survey was conducted also on the same WOCE expedition with shipboard measurements of dissolved inorganic carbon (DIC) done by colilometry and total alkalinity (TA) by potentiometric titration with techniques described in Dickson and Goyet (1994). Some selected sections are shown:temperature, hydrocast salinity, dissolved nitrate, phosphate. ilicate, oxygen, dissolved inorganic carbon,total alkalinity, freon F-11 and freon F-12. Freons distribution showed high concentrations of over 6 pM/kg for F-11 and over 3 pM/kg for F12 in the subsurface shelf waters above 200 in in the shallower portion of Okhotsk Sea at latitudes 56 - 58 degs. N, and also in the open waters over the Derugin and the Kuril Basins. The high freons were acquire d by the shelf waters due to the much higher solubility of freons in seawater at low temperature in pre-winter condition although not dense enough to sink below 200 m. The winter waters dense enough to sink as a plume would be mixed with surrounding waters forming a shelf-derived water (SDW). This SDW would mix isopycnally for sigma-theta) 26.8 to 27.2 with the North Pacific water entering Okhotsk Sea through Kruzenshterna Strait to produce the Sea of Okhotsk Intermediate Water (SOfW). Using CFCs concentrations of SDW, OSIW and NPW at 6,5, 3 and 2.75 pM/Kg respectivelly, the export of Okhotsk Sea Intermediate Water was estimated to be about 5 Sv out of Bussol' Strait as a significant contribution to the North Pacific Intermediate Water, which is about 15 Sv. Distributions of physical and chemical properties with depth show a marked difference between Okhotsk Sea and the North Pacific. In the upper 1,000 m, Okhotsk Sea has lower potential temperature, salinity and nutrients, but higher freons and oxygen than the North Pacific. Below 1,000 m to about 2,000 m, Okhotsk Sea is dominated by a warmer and fresher Deep Water, Below 2,000 m, both Okhotsk Sea waters in the deep Kuril Basin and the North Pacific deep waters have the same physical and chemical characteristics The biogeochemical processes In the Okhotsk Sea basins result in different distribution patterns in the biogenic properties in the water columns. High accumulation of dissolved silicate. nitrate and phosphate, dissolved inorganic carbon (also partial pressure of C02), but lower oxy-en (,i.e. higher A.O.U., apparent oxygen utilization) suggest that active biology in the upper ocean during the summer period led to such distribution mainly in the Deryugin Basin, in contrast to the Kuril Basin. Seasonal studies would be necessary to understand the blogeochemistry of the Okhotsk Sea, an important area of blogenic accumulation influenced by the complex circulation and seasonal ice formation in the upper ocean. REFERENCE: Wong, C.S., R.J. Matear, H.J. Freeland, F.A. Whitney and A.S. Bychkov, Chloroflurocarbons in the Sea of Okhotsk: The role of the Sea of Okhotsk Intermediate Water in the formation of North Pacific Intermediate Water. Submitted to Journal of Geopkysical Research. 1995. Freeland, H.J.,m A.S. Bychkov, F.A. Whitney, c. Taylor, C.S. Wong and G.I. Yurasov, An oceanographic survey through the Sea of Okhotsk: WOCE Survey Line PIW. submitted to Journal of Geophysical Research. 1995. World Ocean Circulation Experiment. WOCE Operations Manual. Vol 3, Section 3. 1, Part 3.1.3. WHP Operations and Methods. WOCE Report No. 68/9 1. November 1994. Dickson, A.G. and C. Goyet. Handbook of methods for the analysis of the various parameters of the carbon dioxide system in sea water. Version 2. U.S. Department of Energy , 1994. +++++ End Item 1 +++++ Item 2 NORTH PACIFIC INTERMEDIATE WATER STUDIED WITH CHEMICAL TRACERS: IS IT ORIGINATED IN THE OKHOTSK SEA? Shizuo Tsunogai and Takayuki Tokieda Marine and Atmospheric Geochemstry Laboratory Graduate School of Environmental Earth Science Hokkaido University Recently the North Pacific Intermediate Water (NPIW) has been paid much attention. This is due to its significant role as a sink of anthropogenic carbon dioxide. Some studies have claimed that the source region of the NPIW is the Okhotsk Sea. To examine this claim, we have studied the NPIW with chemical tracers, although we could not get samples within the Okhotsk Sea. The chemical tracer used are chiefly CFCs which can be used as tracers of waters formed after 1960's and we have also utilized some other chemical tracers such as tritium, C-14 and dissolved silicate. The horizontal and vertical distributions of CFCs were consistent with those of excess total inorganic carbonate of anthropogenic origin. Their concentrations in the surface water are certainly almost saturated and decreased with depth. They were higher in the western part of the North Pacific around 40'N than in the central (and, of course, the eastern) part of the North Pacific in the subsurface water. The maximum penetration depth exceeded 1000 in depth or the surface of (sigma theta of 27.2 in the western North Pacific. It, however, is interesting to note that the old water mixed with the newly formed NPIW is extremely old. In other words, the NPIW is formed by the mixing of cold surface water the deep water. Similar results were obtained from other chemical tracers. For example, the maximum concentration of artificial C-14 in the upper NPIW was found in the latitudinal belt of 40 - 45'N in the western North Pacific. We do not support the idea that the main source region of the NPIW is the Okhotsk Sea. This is due to the following two facts. One is that the maximum concentration of CFCs -at the isopycnal surfaces of the amount of the NPIW estimated from the distribution of CFCs, which is too much to be expected from the cooling within the Okhotsk Sea. +++++ End Item 2 +++++ Item 3 AN ISOTOPIC STUDY ON SEA ICE IN THE SEA OF OKHOTSK Jinro Ukita Dept. of Earth and Planetary Physics Faculty of Science University of Tokyo Noriyuki Tanaka Graduate School of Earth and Environment Science Graduate School Hokkaido University Toshlyuki Kawamura Institute of Low Temperature Science Hokkaido University ABSTRACT The Sea of Okhotsk is a marginal sea adjacent to Pacific Ocean through straits in Kuril Islands, and surrounded by land on three sides; the Kamchatka Peninsula, the Asian continent, and Sakhalin Island. Despite its relatively southern location, its climate is characterized by sea ice in winter when the east-west air pressure gradient associated with Siberian high and Aleutian low results in southward migration of ice that starts in the northwest region of the Sea of Okhotsk. Although this is conjectured earlier by Watanabe (1963), it is only recent that this southward transport of sea ice off Sakhalin Island was confirmed by using the drifting tracks of ARGOS buoys deployed on ice floes (Mochizuki et al, 1995). Besides this general motion, we have very limited information about sea ice formed in the Sea of Okhotsk. Hardly have we -any knowledge about freezing, transport, and melting of sea ice in the region. In an attempt to answer these questions, we conducted isotopic, salinity, and density analyses on sea ice swnples taken from the Sea of Okhotsk On January 27 and 28, 1995, ice sampling was conducted by the Japanese Maritime Safety Agency's ship So-va. The first floe sample (Sample A) was taken very close to the ice edge where ice concentration was 10 - 20 %, and the second floe sample (Sample B) was collected on the following day from an interior area of the ice pack with ice concentration of 80 - 100 %. Then we analyzed the samples using a method similar to the one described by Tucker et al. (1987). Considering the fact that one was taken just a day earlier from the location only 30 - 40 km way, these two Ice Iloes have distinctive features; Sample A with the granular structure and Sample B with the broken columnar structure. The granular feature found in Sample A may be attributed to low ice concentration, which favors for the production of frazil ice by the rough ocean surface condition. On the other hand, Sample B came from an interior area with high ice concentration, which favors for the production of columnar ice and a high level of ridging and rafting activities. They taken togethei account for the broken columnar structure with random orientation of columns found in Sample B. The salinity and density minima along with the abundance of bubbles and opaqueness observed in the top part of Sample A (Figure 1) first led us to believe that this has the snow origin. If this were the case, we can approximately identify the location of its origin from the empirical relationship that exists between isotopic values of precipitation and air temperature (Dansgaard, 1964; Yurtsever, 1975). On the contrary, observed isotope values are substantially higher than the values expected for the snowfall in the Sea of Okhotsk. Typically, an analysis based on the salinity and isotope budget is used to identify the source for-an ice-sea water system (Ostlund and Hut, 1984; Lange et aL, 1990, Macdonald et al., 1995). However, such an analysis fails in this case with unproportionally low density and salinity and high dl8O. The conventional analysis assumes the isotopic fractionation factor for frazil ice is the same as that of sea ice that is formed under relatively quite environment. Thus to clarify the interpretation of the present sample, it seems necessary to conduct basic laboratory and field experiments to estimate the isotopic fractionation factors during the frazil ice production and its dependence on physical environment. In summary, the results from the present analysis suggest the systematic dependence of crystallographic structures on ice concentration and the necessity and importance-of a new experiment for the fractionation factor for frazil ice. REFERENCES Dansgaard, W., 1964: Stable isotopes in precipitation. Tellus, 16, 436-468. Lange, M. A., P. Shlosser, S. F. Ackley, P. Wadhams, and G. S. Dieckmann, 1990: 18O concentrations in sea ice of the Weddell Sea, Antarctica. J. of Glac., 36, 315-323. Macdonald, R.W., D. W. Paton, and E. C. Carmack, 1995: The freshwater budget and under-ice spreading of Mackenzie river water in the Canadian Beaufort Sea based on salinity and 180/160 measurements in water and ice, J. Geoph-vs. Res., 100, 995-919. Mochizuki, S., T. Takatsuka, T. Aota, and P. Tuskov, 1995: Tracing of ice floe in Sea of Okhotsk by satellite-tracked drifters. Abs. on the Tenth Intemational Symposiuni on Okhotsk Sea, Sea Ice and People, The Okhotsk Sea and Cold Ocean Research Association. Monbetsu, Hokkaido. Ostlund, H. G., G. Hut, 1984: Arctic ocean water mass balance from isotope data. J. Geophys. Res., 89, 6373-638 1. Tucker, W. B., A. J. Gow, and W. F. Weeks, 1987: Physical properties of summersea ice in the Fram Strait. J. Geophys. Res., 92, 6787-6803. Yurtsever, Y., 1975: Worldwide survey of stable isotopes in precipitation, Rep. Sect. Isotope Hvdrol., IAEA, 40 pp. Watanabe, K., 1962: Drifted velocities of ice measured from air and separately computed values of their wind-induced and current-induced components - study on sea ice in Okhotsk Sea (11). 7he Oceanographycal Magazine 14, 29-4 1. +++++ End Item 3 +++++ CMR Disclaimer================================================== This document could contain information all or part of which is or may be copyrighted in a number of countries. Therefore, commercial copying and/or further dissemination of this text is expressly prohibited without obtaining the permission of the copyright owner(s) except in the United States and other countries for certain personal and educational uses as prescribed by the "fair copy" provisions of that countries Copyright Statues. ================================================================ ************** END Msg. B.CHM **************