The large reserves of high-grade hematite in the Minas Geraes district of Brazil are also original sediments, but lack the oölitic texture.
An insignificant proportion of the world's iron is obtained from "bog ores," which are sedimentary deposits of hydrated iron oxide in swamps and lakes. These ores have been used only on a small scale and chiefly in relatively undeveloped countries. They are of particular interest from a genetic standpoint in that they show the nature of some of the processes of iron ore deposition as it is actually going on today.
None of the ores of this class, with the exception of the iron carbonates, have undergone any considerable surface enrichment since their primary deposition. Neither, with the exception of the Brazilian ores, have they undergone any deep-seated metamorphism. The shapes, sizes, and distribution of the deposits may be traced back to the conditions of original deposition. In England and western Europe the principal deposits have been only slightly tilted by folding. In the United States the Clinton ores have partaken in the Appalachian folding. In Brazil, the ores have undergone close folding and anamorphism.
2. Deposits of the second class, which owe much of their value to further enrichment since deposition, are represented by the hematite ores of the Lake Superior district. These may be thought of as the locally rusted and leached portions of extensive "iron formations," in which oxidation of the iron, and the leaching of silica and other substances by circulating waters, have left the less soluble iron minerals concentrated as ores. The Lake Superior iron formations now consist near the surface mainly of interbanded quartz (or chert) and hematite, called _jasper_ or _ferruginous chert_ or _taconite_. These are similar in composition to the leaner iron ores of Brazil, called _itabirite_, but differ in that the silica is in the form of chemically deposited chert, rather than fragmental quartz grains.
[Illustration: FIG. 11. Alteration of Lake Superior iron formation to iron ore by the leaching of silica.]
When originally deposited the iron was partly hematite (perhaps some magnetite) and largely in the form of iron carbonate (siderite) and iron silicate (greenalite), interbanded with chert. The original condition is indicated by the facts that deep below the surface, in zones protected from weathering solutions, siderite and greenalite are abundant, and that they show complete gradation to hematite in approaching the surface. The ore has been concentrated in the iron formation almost solely by the process of leaching of silica by surface or meteoric waters, leaving the hematite in a porous mass. Figure 11 illustrates this change as calculated from analyses and measurements of pore space. During this process a very minor amount of iron has been transported and redeposited. In short, the Lake Superior iron ores are residual deposits formed by exactly the same weathering processes as cause the accumulation of clays, bauxites, and the oxide zones of sulphide deposits. The development of an iron ore rather than of other materials as an end-product is due merely to the peculiar composition of the parent rock. The solution of silica on such an immense scale as is indicated by these deposits has sometimes been questioned on the general ground that silica minerals are insoluble. However, there is plenty of evidence that such minerals _are_ soluble in nature; and the assumption of insolubility, so often made in geologic discussions, is based on the fact that most other minerals are _more_ soluble than silica minerals, and that in the end-products of weathering silica minerals therefore usually remain as important constituents. Iron oxide, on the other hand, is _less_ soluble even than silica,--with the result that when the two occur together, the evidence of leaching of silica from the mixture becomes conspicuous.