Generation of metal deposits on the sea floor

1976 ◽  
Vol 13 (1) ◽  
pp. 126-135 ◽  
Author(s):  
B. J. Fryer ◽  
R. W. Hutchinson

Recent studies of volcanogenic base metal sulfide deposits and of metalliferous sediments in the Red Sea indicate precipitation of iron and base metals under conditions varying from reducing to oxidizing, at or near sites of fumarolic brine emission onto the sea floor. Differing lithofacies of iron-rich sediments were apparently deposited penecontemporaneously, mainly in response to changing chemical, biological, and sedimentary lithofacies conditions.Iron-rich sediments associated with the cupriferous pyrite bodies of Cyprus have been studied to determine the behavior of Fe, Mn, Cu, Zn, Pb, Ni, Co, Cr, Sn, Mo, Ag, and Au, when these fumarolic brines enter the sea bottom environment. Variations in metal abundances and ratios indicate that rapidly changing Eh is a major factor controlling metal deposition on the sea floor. The Fe/Mn ratio in these sediments is a useful indicator of the amount of interaction of these fumarolic brines and normal oxygenated sea water. Results suggest that zinc, copper, and gold are concentrated in the high Fe/Mn ratio proximal sediments; nickel is concentrated in the low Fe/Mn ratio distal sediments; and lead, silver, tin, and molybdenum are relatively unaffected by oxidation of the fumarolic brine solution by normal sea water.These concepts of sea floor deposition controlling the distribution of metals may also be applicable to other types of stratabound metalliferous deposits, like certain skarn, greisen, and gold ores, heretofore considered to be of epigenetic origin.

2019 ◽  
Vol 114 (3) ◽  
pp. 473-512 ◽  
Author(s):  
Katherine S. Frank ◽  
Paul G. Spry ◽  
Hein Raat ◽  
Rodney L. Allen ◽  
Nils F. Jansson ◽  
...  

1979 ◽  
Vol 22 (86) ◽  
pp. 67-81 ◽  
Author(s):  
V. L. Tsurikov

Abstract The different factors contributing to the formation of the gas porosity of sea ice are: (Ia) gases captured during the formation of the initial ice cover, (Ib) gases released from solution during the initial freezing of sea-water, (Ic) the inclusion of gases rising from the sea bottom, (2a) the substitution of gas for brine drained from the ice during times of melting, (2b) the release of gas from the brine within the ice during the course of partial freezing, and (2c) the formation of voids filled with water vapour during the course of internal melting. An analysis is made of each of these processes and it is concluded that processes Ib, 2a, and 2C are important. Process Ic may also be a major effect but it is difficult to evaluate until the rate of gas release from the sea floor is better known. The migration of air pockets into the ice from the overlying snow is shown to be a possible but not a significant effect. Available data on the composition of gas in sea ice are reviewed and it is shown to be significantly different from air. Possible causes for these differences are discussed. The porosity of sea ice, i.e. the total relative volume of its gas plus its brine inclusions, is one of the factors strongly affecting its strength, as has been shown by Tsurikov (1947) and by Weeks and Assur (1968). In seas with high salinities the effect of the presence of brine within the ice will usually be the dominant factor. However on water bodies with low salinities the effect of the gas included within the ice may be greater than the effect of the brine. Despite its significance there have not been any attempts at a quantitative analysis of the entrapment of gas in sea ice. This paper is an attempt at such a study.


1970 ◽  
Vol 7 (3) ◽  
pp. 1012-1017
Author(s):  
C. D. Anderson ◽  
H. G. Sherwood

Ore-density measurements were made on representative samples from thirty-seven base-metal deposits. Thirty-five of these samples were mill-feed composites and two were drill-core composites. The values obtained ranged from 2.73 g/cm3 to 4.53 g/cm3. The median density was 3.20 g/cm3.


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