Of the common rocks and minerals figuring as the more abundant materials of the earth's crust, only a few are prominently represented in the tables of mineral resources. Of these water and soils stand first. Others are the common igneous and sedimentary rocks used for building and road materials. Missing from the lists of the most abundant minerals and rocks, are the greater part of the commercially important mineral resources—including such as coal, oil, gas, iron ore, copper, gold, and silver,—implying that these mineral products, notwithstanding their great absolute bulk and commercial importance, occur in relatively insignificant amounts as compared with the common rock minerals of the earth.
The common rocks and minerals develop in a general sequence, starting with igneous processes, and passing through stages of weathering, erosion, sedimentary processes, and alterations beneath the surface. The commercial minerals are incidental developments under the same processes.
The earliest known rocks are largely igneous. Sedimentary rocks are formed from the breaking down of igneous rocks, and the origin of rocks therefore starts with the formation of igneous rocks. Igneous rocks are formed by the cooling of molten rock material. The ultimate source of this molten material does not here concern us. It may come from deep within the earth or from comparatively few miles down. It may include preëxisting rock of any kind which has been locally fused within the earth. Wherever and however formed, its tendency is to travel upward toward the surface. It may stop far below the surface and cool slowly, forming coarsely crystallized rocks of the granite and gabbro types. Igneous rocks so formed are called plutonic intrusive rocks. Or the molten mass may come well toward the surface and crystallize more rapidly into rocks of less coarse, and often porphyritic, textures. Such intrusive rocks are porphyries, diabases, etc. Or the molten mass may actually overflow at the surface or be thrown out from volcanoes with explosive force. It then cools quickly and forms finely crystalline rocks of the rhyolite and basalt types. These are called effusives or extrusives, or lavas or volcanics, to distinguish them from intrusives formed below the surface. The intrusive masses may take various forms, called stocks, batholiths, laccoliths, sills, sheets and dikes, definitions and illustrations of which are given in any geological textbook. The effusives or volcanics at the surface take the form of sheets, flows, tuffs, agglomerates, etc.
Some of the igneous rocks are themselves "mineral" products, as for instance building stones and road materials. Certain basic intrusive igneous rocks contain titaniferous magnetites or iron ores as original constituents. Others carry diamonds as original constituents. Certain special varieties of igneous rocks, known as pegmatites, carry coarsely crystallized mica and feldspar of commercial value, as well as a considerable variety of precious gems and other commercial minerals. Pegmatites are closely related to igneous after-effects, discussed under the next heading. As a whole, the mineral products formed directly in igneous rocks constitute a much less important class than mineral products formed in other ways, as described below.
Igneous after-effects. The later stages in the formation of igneous rocks are frequently accompanied by the expulsion of hot waters and gases which carry with them mineral substances. These become deposited in openings in adjacent rocks, or replace them, or are deposited in previously hardened portions of the parent igneous mass itself. They form "contact-metamorphic" and certain vein deposits. Pegmatites, referred to above, are in a broad sense in this class of "igneous after-effects," in that they are late developments in igneous intrusions and often grade into veins clearly formed by aqueous or gaseous solutions. Among the valuable minerals of the igneous after-effect class are ores of gold, silver, copper, iron, antimony, mercury, zinc, lead, and others. While mineral products of much value have this origin, most of them have needed enrichment by weathering to give them the value they now have.
No sooner do igneous rocks appear at or near the earth's surface, either by extrusion or as a result of removal by erosion of the overlying cover, than they are attacked vigorously by the gases and waters of the atmosphere and hydrosphere as well as by various organisms,—with maximum effect at the surface, but with notable effects extending as far down as these agents penetrate. The effectiveness of these agents is also governed by the climatic and topographic conditions. Under conditions of extreme cold or extreme aridity, weathering takes the form mainly of mechanical disintegration, and chemical change is less conspicuous. Under ordinary conditions, however, processes of chemical decomposition are very apparent. The result is definitely known. The rocks become softened, loose, and incoherent. Voids and openings appear. The volume tends to increase, if all end products are taken into account. The original minerals, largely feldspar, ferro-magnesian minerals, and quartz, become changed to clay, mixed with quartz or sand, calcite or dolomite, and iron oxide, together with residual particles of the original feldspars and ferro-magnesian minerals which have only partly decomposed. In terms of elements or chemical composition, water, oxygen, and carbon dioxide, all common constituents of the atmosphere and hydrosphere, have been added; and certain substances such as soda, potassa, lime, magnesia, and silica have in part been carried away by circulating waters, to be redeposited elsewhere as sediments, vein fillings, and cements. Figure 1 illustrates the actual mineral and volume changes in the weathering of a granite—one of the most common rocks. The minerals anorthite, albite, and orthoclase named in this figure are all feldspars; sylvite and halite are chlorides of potash and soda. The weathering processes tend to destroy the original minerals, textures, and chemical composition. They are collectively known as katamorphic alterations, meaning destructive changes. The zone in which these changes are at a maximum is called the zone of weathering. This general zone is principally above the surface or level of the ground-waters, but for some rocks it extends well below this level. In some regions the ground-water level may be nearly at the surface, and in others, especially where arid, it may be two thousand or more feet down. Disintegrated weathered rocks form a blanket of variable thickness, which is sometimes spoken of as the residual mantle, or "mantle rock."
Mineral products formed by weathering from common igneous rocks include soils, clay, bauxite, and certain iron, chromite, and nickel ores. Again the commercial importance of this group is not large, as compared with products formed in other ways described below.
The same weathering processes described above for igneous rocks cause considerable changes of economic significance in deposits formed as igneous after-effects. In some cases they result in removing the less valuable minerals, thus concentrating the more valuable ones, as well as in softening the rock and making it easier to work; and in other cases they tend to remove the valuable constituents, which may then be redeposited directly below or may be carried completely out of the vicinity. The oxide zones of many ore bodies are formed by these processes.
Sedimentary rocks are formed by the removal and deposition of the weathered products of a land surface. Air, water, and ice, moving under the influence of gravity and other forces, all aid in this transfer. The broken or altered rock materials may be merely moved down slopes a little way and redeposited on the surface, forming one type of terrestrial or subaërial deposits, or they may be transferred and sorted by streams. When deposited in streams or near their mouths, they are known as river, alluvial, or delta deposits. When carried to lakes and deposited they form lake deposits. Ultimately the greater part of them are likely to be carried to the ocean and deposited as marine sediments.
Part of the weathered substances are carried mechanically as clay and sand, which go to make up the shale and sandstone sediments. Part are carried in solution, as for example lime carbonate and magnesium carbonate, which go to make up limestone and dolomite. Some of the dissolved substances are never redeposited, but remain in solution as salts in the sea, the most abundant of which is sodium chloride. Some of the dissolved substances of weathering, such as calcite, quartz, and iron oxide, are carried down and deposited in openings of the rocks, where they act as cements.
The sediments as a whole consist of three main types,—shales (kaolin, quartz, etc.), sandstones (quartz, feldspar, etc.), and limestones or dolomites (carbonates of lime and magnesia). Of these, the shale group is by far the most abundant. There are of course many sediments with composition intermediate between these types. There are also sediments made up of large undecomposed fragments of the original rocks, cemented to form conglomerates, or made up of small fragments of the original rocks cemented to form arkoses and graywackes. These, however, may be regarded as simply stages in the alteration, which in repeated cycles of weathering must ultimately result in producing the three main groups,—shales, sandstones, and limestones.
Mineral products formed by sedimentary processes include sandstones, limestones, and shales, used as building stone and road materials; certain sedimentary deposits of iron, like the Clinton ores of the southeastern United States and the Brazilian ores; important phosphate deposits; most deposits of salt, gypsum, potash, nitrates, etc.; comparatively few and unimportant copper deposits; and important placer deposits of gold, tin, and other metals, and precious stones. With the aid of organic agencies, sedimentary processes also account for the primary deposition of coal and oil.
After sedimentary rocks are formed, and in many cases covered by later sediments, they may be brought again by earth movements and erosion to the surface, where they in turn are weathered. The weathering of sedimentary rocks proceeds along lines already indicated for the igneous rocks. Residual mantles of impure clay and sand are commonly formed. The mineral composition of sedimentary rocks being different from that of igneous rocks to start with, the resulting products are in slightly different proportions; but the changes are the same in kind and tend merely to carry the general process of alteration farther in the same direction,—that is, toward the production of a few substances like clay, quartz, iron oxide, and calcite, which are transported and redeposited to form clay, sand, and limestone. Cycles of this kind may be repeated indefinitely.
By weathering of sedimentary rocks are produced some soils, certain commercial clays, iron ores, lead and zinc ores, and other valuable mineral products.
Cementation. No sooner are residual weathered mantles formed or sedimentary rocks deposited, whether under air or water, than processes of consolidation begin. Settling, infiltration of cementing materials, and new growths, or recrystallization, of the original minerals of the rock all play a part in the process. The mud or clay becomes a shale, the sand becomes sandstone or quartzite, the marl becomes limestone or marble. All the minute openings between the grains, as well as larger openings such as fissures and joints, may thus be filled. At the same time the cementing materials may replace some of the original minerals of the rock, the new minerals either preserving or destroying the original textures. This process is sometimes called metasomatic replacement. Igneous rocks as a rule are compact, and hence are not so much subject to the processes of cementation as sedimentary rocks; but certain of the more porous phases of the surface lavas, as well as any joints in igneous rocks, may become cemented. All of these changes may be grouped under the general term cementation.
A special phase of consolidation and cementation is produced near intrusive igneous rocks through the action of the heat and pressure and the expelled substances of the igneous rock. This is called contact metamorphism or thermal metamorphism. The processes are even more effective when acting in connection with the more intense metamorphism described under the next heading.
By cementation some of the common rocks, especially the sediments, become sufficiently compact and strong to be useful as commercial products, such as building stones and road materials.
More important as mineral products are the cementing materials themselves. These are commonly quartz, calcite, or iron oxide, of no especial value, but locally they include commercially valuable minerals containing gold, copper, silver, lead, zinc, and many other mineral products.
It is a matter of simple and direct observation, about which there is no controversy, that many minerals are deposited as cements in the openings in rocks or replacing rocks. As to the source of the solutions bringing in these minerals, on the other hand, there has been much disagreement. In general, the common cementing materials such as quartz and calcite, as well as some of the commercial minerals, are clearly formed as by-products of weathering, and are transported and redeposited by the waters penetrating downward from the surface. The so-called secondary enrichment of many valuable veins is merely one of the special phases of cementation from a superficial source. In other cases it is believed that deep circulation of ordinary ground-waters may pick up dispersed mineral substances through a considerable zone, and redeposit them in concentrated form in veins and other trunk channels. For still other cementing materials, it is suspected that the ultimate source is in igneous intrusions; in fact, deposits of this general character show all gradations from those clearly formed by surface waters, independently of igneous activity, to those of a contact-metamorphic nature and others belonging under the head of "igneous after-effects."
Hypothesis and inference play a considerable part in arriving at any conclusion as to the source of cementing materials,—with the result that there is often wide latitude for difference of opinion and of emphasis on the relative importance of the different sources of ore minerals.
Dynamic and contact metamorphism. Beneath the surface rocks are not only cemented, but may be deformed or mashed by dynamic movements caused by great earth stresses; the rocks may undergo rock flowage. The result is often a remarkable transformation of the character of the rocks, making it difficult to recognize their original nature. Also, igneous intrusions may crowd and mash the adjacent rocks, at the same time changing them by heat and contributions of new materials. This process may be called contact metamorphism, but in so far as it results in mashing of the rocks it is closely allied to dynamic metamorphism. The former term is also applied to less profound changes in connection with igneous intrusions, which result merely in cementation without mashing.
Dynamic and contact metamorphism may in some cases produce rocks identical in appearance with those produced by ordinary processes of cementation and recrystallization without movement. For instance, it is difficult to tell how much movement there has been in the production of a marble, because both kinds of processes seem to produce much the same result. Commonly, however, the effect of dynamic metamorphism is to produce a parallel arrangement of mineral particles and to segregate the mineral particles of like kind into bands, giving a foliated or schistose or gneissic structure, and the rocks then become known as slates, schists, or gneisses. Commonly they possess a capacity to part along parallel surfaces, called cleavage. The development of the schistose or gneissic structure is accompanied by the recrystallization of the rock materials, producing new minerals of a platy or columnar type adapted to this parallel arrangement. Even the composition of the rock may be substantially changed, though this is perhaps not the most common case. Whereas by weathering the rock is loosened up and disintegrated, substances like carbon dioxide, oxygen, and water are abundantly added, and light minerals of simple composition tend to develop,—by dynamic metamorphism on the other hand, carbon dioxide, oxygen, and water are usually expelled, the minerals are combined to make heavier and more complex minerals, pore space is eliminated, and altogether the rock becomes much more dense and crystalline. While segregation of materials is characteristic of the surficial products of weathering, the opposite tendency, of mixing and aggregation, is the rule under dynamic metamorphism, notwithstanding the minor segregation above noted.
Dynamic metamorphism is for the most part unfavorable to the development of mineral products. Ore bodies brought into a zone where these processes are active may be profoundly modified, but not ordinarily enriched. One of the exceptions to this general rule is the development of the cleavage of a slate, which enables it to be readily split and thereby gives it value. Contact metamorphism, on the other hand, may develop valuable mineral deposits (see pp. 20, 45-46).
All of the chemical, mineralogical, and textural changes in rocks above described may be collectively referred to as metamorphism. The phase of metamorphism dealing with surficial weathering, similar changes below the surface, and the formation of sediments, is called katamorphism or destructive change. The phase of metamorphism dealing with the constructive changes in rocks, due to cementation, dynamic movements, and igneous influences, is called anamorphism. Some geologists confine the term metamorphism to the changes involved in contact and dynamic metamorphism, and call the resulting products metamorphic rocks.
The zone in which katamorphism is most active, usually near the surface, is called the zone of katamorphism. The deeper zone in which anamorphism is preponderant is called the zone of anamorphism. There are no definite limits of depth to these zones. A given rock may be undergoing katamorphism while rocks on either side at the same depth are suffering anamorphism.
By katamorphism rocks break down to produce the surficial rocks, and by anamorphism the surficial rocks are again consolidated and altered to produce highly crystalline rocks, which are not dissimilar in many of their characteristics to the igneous rocks from which all rocks trace their ultimate origin. In other words, anamorphism tends toward the reproduction of igneous rocks, though it seldom fully accomplishes this result. These two main groups of changes together constitute the metamorphic cycle. Some rocks go through all phases of the cycle, but others may pass directly from one phase to an advanced phase without going through the intermediate stages. For instance, an igneous rock may become a schist without going through the intermediate stage of sedimentation.
Rocks are not permanent in their condition, but at practically all times and places are undergoing some kind of metamorphism which tends to adapt them to their environment. The conception of rocks as representing phases or stages in a progressive series of changes called the metamorphic cycle aids greatly in correlating and holding in mind many details of rock nature and origin, and brings into some sort of perspective the conditions which have produced rocks. A schistose sediment comes to be regarded as an end product of a long series of alterations, beginning with igneous rocks and passing through the stages of weathering, sedimentation, cementation, etc., each of which stages has been responsible for certain mineralogical, chemical, and textural features now characterizing the rock. The alternation of constructive and destructive changes of the metamorphic cycle, and the repetitions of the cycle itself, periodically work over the earth materials into new forms. Usually the cycles are not complete, in the sense that they seldom bring the rock back to exactly the same condition from which it started. More sediments are formed than are changed to schists and gneisses, and more schists and gneisses are formed than are changed back to igneous rocks. Salts in the ocean continuously accumulate. The net result of the metamorphic cycle, is, therefore, the accumulation of materials of the same kinds. Incidental to these accumulations is the segregation of commercial mineral products.
The metamorphic cycle becomes a logical and convenient geologic basis for correlating, interpreting, and classifying mineral products. Because of the great variety of materials and conditions represented in mineral deposits, prodigious efforts are required to remember them as independent entities; but as incidents or stages in the well-known progress of the metamorphic cycle, their essential characteristics may be easily remembered and kept in some perspective.
Ores of certain metals, such as iron, occur in almost every phase of the metamorphic cycle,—as igneous after-effects, as weathered products, as sediments, and as schists. The ores of each of these several phases have group characteristics which serve to distinguish them in important particulars from ores belonging to other phases of the cycle. Having established the position of any particular ore in the metamorphic cycle, a number of safe inferences are possible as to mineralogical composition, shape, extent, and other conditions, knowledge of which is necessary for an estimate of commercial possibilities.
[1] Clarke, F. W., Data of geochemistry: Bull. 695, U. S. Geol. Survey, 1920, p. 35.
[2] Clarke, F. W., Data of geochemistry: Bull. 695, U. S. Geol. Survey, 1920, p. 33.
[3] Clarke, F. W., Data of geochemistry: Bull. 695, U. S. Geol. Survey, 1920, pp. 22-23.
Mineral products may be classified according to use, commercial importance, geographic distribution, form and structure, mineralogical and chemical composition, or origin. Each of these classifications is useful for some purposes. The geologist usually prefers a classification based on origin or genesis. In the following chapters on mineral resources, however, such a classification is not the primary one, because of the desire to emphasize economic features. The mineral commodities are treated as units and by group uses. Some mineral commodities have so many different kinds of origin in different regions that to distribute them among several genetic groups in description would make it impossible to preserve the unity necessary for consideration of the economic features.
While in the descriptive chapters many references are made to origin, it may be difficult for the reader to assemble them in perspective; for this reason we summarize at the outset some of the salient features of origin of mineral deposits and of their geologic classification.
To the layman the reason for emphasis on origin is often not clear. The "practical" man frequently regards this phase of the subject as merely incidental to the immediate economic questions—a playground for harmless theorists. The answer of the economic geologist is that in no other way than by a knowledge of origin is it possible to arrive at an understanding of conditions which so well enables one to answer many practical questions. In the exploration for mineral deposits, it is obvious that an understanding of the kinds of geologic conditions and processes under which a given type of deposit is known to develop results in the elimination of much unpromising territory, and the concentration of work on favorable localities. In forming any estimate of mineral deposits beyond the ground immediately opened up,—for instance, in estimating depth, form, change in values, mineralogical character, or interruptions due to faulting,—it is difficult to form any intelligent conception of the probabilities unless the history of the deposit is understood. If, for instance, the ore is known to be formed by hot waters, associated with the cooling of igneous rocks, different conditions are to be expected below the zone of observation than if the ore is formed by surface waters. If the ore body is formed as a single episode under simple geologic conditions, the interpretation of the possibilities in the situation may be quite different from the interpretation applied where the history has been more complex. If the surface conditions suggest possibilities of secondary enrichment of the ores, the interpretation of the conditions underground will be different from those applied where there is no evidence of such enrichment.
Where a mineral deposit is completely opened up in three dimensions, it is often possible to work out economic questions of tonnage, grade, shape, and values, without the aid of geology. Also, where conditions are comparatively simple and uniform throughout a district, the local knowledge of other mines may be a sufficient basis for answering these questions for any new property developed. Empirical methods may suffice. However, it is seldom that the conditions are so simple that some geological inference is not necessary. Even where problems are settled without calling in the geologist, geological inferences are required in the interpretation of, and projection from, the known facts. It is often the case that the practical man has in his mind a rather elaborate assortment of geologic hypotheses, based on his individual experience, which make the so-called theories of the geologist seem conservative in comparison. The geologist comes to the particular problem with a background of established geologic principles and observations, and his first thought is to ascertain all the local conditions which will aid in deciphering the complete history of the mineral deposit. There is no fact bearing on the history, however remote from practical questions, which may not be potentially valuable.
With this digression to explain the geologist's emphasis on origin of mineral products, we may return to a consideration of a few of the principles of rock and mineral genesis which have been found to be significant in the study of mineral products.
In the preceding chapters it has been indicated that mineral deposits are mere incidents in the mass of common rocks; that they are made by the same processes which make common rocks, that none of the processes affecting mineral deposits are unique for these minerals, and that most common rocks are on occasion themselves used as mineral resources. These facts are emphasized in order to make it clear that the study of mineral deposits cannot be dissociated from the study of rocks, and that the study of the latter is essential to bring mineral deposits into their proper perspective. Absorption in the details of a mineral deposit makes it easy for the investigator to forget or minimize these relations.
Nevertheless, in the study of mineral deposits, and especially deposits of the metallic minerals, certain geologic features stand out conspicuously against the common background indicated above. Our discussion of these features will follow the order of rock genesis indicated in the description of the metamorphic cycle.
Any classification of mineral deposits on the basis of origin is more or less arbitrary. The sharp lines implied by the use of class names do not exist in nature. Mineral deposits are so complex and so interrelated in origin, that a classification according to genesis indicates only the essential and central class features; it does not sharply define the limits of the classes.
It is practically impossible for any geologist to present a classification which will be accepted without qualification by other geologists, although there may be agreement on essential features. Difficulties in reaching agreement are increased by the inheritance from the past of names, definitions, and classifications which do not exactly fit present conceptions based on fuller information,—but which, nevertheless, have become so firmly established in the literature that it is difficult to avoid their use. In the progress of investigation many new names are coined to fit more precisely the particular situation in hand, but only in fortunate cases do these new names stand up against the traditional currency and authority of old names. The geologist is often in despair in his attempt to express his ideas clearly and precisely, and at the same time to use terms which will be understandable by his readers and will not arouse needless controversy.
As illustrative of the above remarks reference may be made to a few terms commonly used in economic geology, such as primary, secondary, syngenetic, epigenetic, supergene, hypogene, protore, etc.
The most commonly used of these terms are primary and secondary. It is almost impossible to define them in a way which will cover all the conceptions for which they have been used, and yet in their context they have been very useful in conveying essential ideas. An ore formed by direct processes of sedimentation has sometimes been called primary, whereas an ore formed by later enrichment of these sediments has been called secondary. An ore formed directly by igneous processes has been called primary, while an ore formed by enrichment of such primary ore by later processes has been called secondary. It is clear, however, that these terms are merely relative, with application to a specific sequence, and that they do not fix the absolute position of the ore in a sequence applying to all ores. For instance, ores deposited directly as sediments or placers may be derived from the erosion of preëxisting ore bodies,—in which case it may sometimes be convenient to refer to the sedimentary ores or placers as secondary and the earlier ores as primary. Or a sulphide deposit originating through igneous agencies may undergo two or three successive enrichments, each successive one secondary to the preceding, but primary to the one following. In spite of these obvious difficulties, the terms primary and secondary may be entirely intelligible as indicating relative order of development under a given set of conditions.
The term syngenetic has been used for mineral deposits formed by processes similar to those which have formed the enclosing rocks and in general simultaneously with them, and epigenetic for those introduced into preëxisting rocks. In certain cases syngenetic may be roughly synonymous with primary, and epigenetic with secondary, and yet a primary ore may be epigenetic. For instance, zinc sulphides in the Mississippi valley limestones (pp. 54-55) are epigenetic, and yet are primary with reference to a later enrichment. The two sets of terms are meant to convey somewhat different ideas and are not interchangeable.
Ransome[4] has suggested, especially for vein and contact deposits, a series of names which has the considerable advantage of definiteness:—hypogene ores, formed in general by ascending non-oxidizing solutions, perhaps hot; supergene ores, formed in general by oxidizing and surface solutions, initially cold and downward moving; and protores, or metallized rock or vein substances which are too low in tenor to be classed as ores, but which would have been converted into ores had the enriching process been carried far enough. In this connection Ransome defines primary ore as unenriched material that can be profitably mined. In view of the general use of the terms primary and secondary as expressing a sequential relation of ore development, it is doubtful whether this more precise definition will supersede the older usage. Also it may be noted that commercial conditions might require, under these definitions, the designation of an ore as a protore at one time or place and as a primary ore at another. Hypogene ores are dominantly primary, and supergene ores are dominantly secondary, but either may include both primary and secondary ores.
The terms of these several classifications overlap, and seek to express different aspects of the same situation. While almost synonymous in certain applications they are not in others.
In this text the writer has certainly not escaped the difficulties in regard to names above referred to, nor in fact has he made any exceptional effort to do so. His chief purpose is to convey, in somewhat elementary terms, an understandable idea of the central features of economic geology. In the main, the most widely accepted terms are used. Almost at every turn it would be possible, in the interests of precision, to introduce qualifying discussions of names,—but at the expense of continuity and perspective in the presentation of the principal subject-matter. The writer does not wish to minimize the necessity for careful and precise nomenclature; but he regards it important that the student focus his attention on the central objective facts of the subject, and that he do not become misled by the sometimes over-strenuous advocacy of certain names or classifications in preference to others. If the facts are understood, he will ordinarily have no difficulty in judging the significance of the variety of names proposed to express these facts. If, on the other hand, the student approaches the subject with a ready-made set of names and definitions learned by rote, he is in danger of perceiving his facts from one angle only and through a distorted perspective.
In this class are included deposits which crystallize within the body of igneous rock, almost, if not quite, simultaneously with the adjacent rock. These deposits form one of the main types of syngenetic deposits.
The titaniferous magnetites constitute a widely distributed but at present commercially unavailable class of iron ores. The magnetite crystals of these deposits interpenetrate with the other constituents of an igneous rock, commonly of a gabbro type, and the deposits themselves are essentially igneous rocks. Their shapes are for the most part irregular, their boundaries ill-defined, and their concentration varying. While their magmatic origin is clear, there is little agreement as to the precise conditions which determined their segregation in the molten rock. There is often a tendency for the ores to follow certain primary sheeted structures in the igneous mass, a fact for which the reason is not obvious.
The Sudbury nickel ores, of Ontario, Canada, the principal source of the world's nickel, lie mainly within and along the lower margin of a great intrusive igneous mass of a basic type called norite, and locally the ores project beyond the margin into adjacent rocks. Their textures and their intercrystallization with the primary minerals of the igneous rock have suggested that they are essentially a part of the norite mass, and that they crystallized during some segregative processes which were effective before the magma had solidified. Near the ores there are likely to be granitic rocks, which, like the ores, seem to be segregations from the norite magma. Locally both the ores and the associated granitic rocks replace the main norite body in such a fashion as to indicate their slightly later crystallization. However, the intimate association of the ores with the primary minerals in the magma, together with their absence from higher parts of the norite and from the extraneous rocks far from the contact, indicate to other investigators that they were not brought in from outside in vagrant solutions which followed the intrusion of the main magma, but that they were segregated within the magma essentially in place. The occurrence of these heavy ores near the base of the norite naturally suggests that they were segregated by sinking to the bottom of the molten magma, but this conclusion implies certain physical conditions of the magma which have not yet been proved. Again the precise nature of the process and the part played in it by aqueous and gaseous solutions are subject to some doubt and controversy. The settlement of this problem awaits the solution of the more general problem of the origin and crystallization of magmas.
In this general class of igneous deposits may be mentioned also diamonds, platinum, chromite, corundum, and other mineral products, although for the formation of commercial ores of many of these substances further concentration by weathering and sedimentation has been required.
Pegmatites are coarsely crystalline acid dike rocks which often accompany a large igneous intrusion and which have obviously crystallized somewhat later than the main igneous mass. They may constitute either sharply delimited dikes or more irregular bodies which grade into the surrounding igneous mass. They have a composition roughly similar to the associated igneous rock, but usually a different proportion of minerals. They are probably the result of the differentiation of the parent magma. The pegmatites are of especial interest to the economic geologist because of the frequency with which they carry commercial minerals, such as the precious stones, mica, feldspar, cassiterite (tin ore), and others. They show a complete gradation from dikes of definitely igneous characteristics to veins consisting largely of quartz in which evidence of igneous origin is not so clear. The pegmatites thus afford a connecting link between ores of direct igneous sources and ores formed as "igneous after-effects," which are discussed in the next paragraph. Aplites are fine-grained acid igneous rocks of somewhat the same composition as the pegmatites and often show the same general relations to ores.
These deposits are closely associated in place and age with igneous rocks, either intrusive or extrusive, and are usually considered to have come from approximately the same source; and yet they afford distinct evidence of having been deposited after the adjacent igneous rocks were completely crystallized and fractured. They are thus epigenetic deposits. They are not themselves igneous rocks and they do not constitute pegmatites, but they often grade into pegmatites and belong to the same general stage in the sequence of events. They include deposits formed by contact metamorphism. They are sometimes designated by the general term "igneous after-effects"—a term also applied in some cases to pegmatites. Some geologists discriminate between "deep vein" deposits (p. 43) and "contact-metamorphic" deposits, but the two are so closely related in place and origin that for our purposes they will be considered together.
The ores of this class are clearly deposited from vagrant solutions which wander through openings of all kinds in the igneous rock and outward into the adjacent country rocks. They also replace the wall rocks; limestone is especially susceptible. This is a phase of contact metamorphism. Some of the most important metalliferous deposits belong in this class, including most of the gold, silver, copper, iron, lead and zinc ores of the western United States and the copper deposits of Lake Superior.
In general, ores of this class are more abundant about intrusive igneous rocks, that is about igneous rocks which have stopped and cooled before reaching the surface,—than in association with extrusive igneous rocks which have poured over the surface as lava flows—but the latter are by no means insignificant, including as they do such deposits as the Lake Superior copper ores, the Kennecott copper ores of Alaska, some of the gold-silver deposits of Goldfield and other Nevada camps, and many others.
There is general similarity in the succession of events shown by study of ore bodies related to intrusives. First, the invasion of the magma, resulting in contact metamorphism of the adjacent rocks, sometimes with, and often without conspicuous crowding effects on the invaded rocks; second, the cooling, crystallization, and cracking of both the igneous rock and the adjacent rock; third, the introduction of ore-bearing solutions into these cracks,—sometimes as a single episode, sometimes as a long continued and complex process forming various types of minerals at successive stages. This order may in some cases be repeated in cycles, and overlapping of the successive events is a common feature.
One of the interesting facts is the way in which the igneous mass has invaded and extensively altered the country rocks in some mineral districts,—in some cases by crowding and crumpling them, and in others without greatly disturbing their structural attitudes. The latter is illustrated in the Bingham district of Utah and the Philipsburg district of Montana. In such cases there is so little evidence of crowding of the country rocks as to raise the question how such large masses of intrusives could be introduced without greater disturbing structural effect. This leads naturally to consideration of the general problem of the manner of progress of magmas through adjacent rocks,—a subject which is still largely in the realm of speculation, but which is not thereby eliminated from the field of controversy. Facts of this kind seem to favor the position of certain geologists that magmas may assimilate the rocks they invade.
No one ever saw one of these deposits in the process of formation; the conclusion, therefore, that they originated from hot solutions, either aqueous or gaseous, or both, which were essentially "after-effects" of igneous activity and came from the same primary source as the associated igneous rocks, is an inference based on circumstantial evidence of the kind below summarized:
(1) The close association both in place and age with igneous rocks. This applies not only to individual deposits, but to certain groups of deposits which have common characteristics, and which constitute a metallogenic province; also to groups of the same geologic age, which indicate a metallogenic epoch (pp. 308-309). The association with igneous rocks in one place might be a coincidence but its frequent repetition can hardly be so explained. A zonal arrangement of minerals about intrusives is often noted. Geologic evidence often shows the processes of ore deposition to have been complete before the next succeeding geologic event,—as for instance in the Tonopah district of Nevada (p. 236), where the ores have been formed in relation to certain volcanic flows and have been covered by later flows not carrying ore, without any considerable erosion interval between the two events.
(2) The general contrast in mineralogical and chemical composition, texture, and mineral associations, between these ore minerals and the minerals known to be formed by ordinary surficial agencies under ordinary temperatures. The latter carry distinctive evidences of their origin. When, therefore, a mineral group is found which shows contrasting evidences, it is clear that some other agencies have been at work; and the natural assumption is that the solutions were hot rather than cold; that they came from below rather than above.
(3) The contrast between the character and composition of these ores (and their associated gangue) and the character and composition of the wall rocks, together with the absence of leaching of the wall rocks, favor the conclusion that the ore minerals are foreign substances introduced from extraneous sources. The source not being apparent above and the processes there observed not being of a kind to produce these results, it is concluded that the depositing solutions were hot and came from below.
(4) The fact that many of the ore minerals are never known to develop under ordinary temperatures at the surface. For some of them, experimental work has also indicated high temperature as a requisite to their formation.
Quartz, which is a common associate of the ores and often constitutes the principal gangue, serves as a geologic thermometer in that it possesses an inversion point or temperature above which it crystallizes in a certain form, below which in another. In deposits of this class it has often been found to crystallize at the higher temperatures.
The quartz sometimes shows bubbles containing liquid, gas, and small heavy crystals, probably of ferric oxide, as in the Clifton-Morenci district of Arizona. It is clear that the ore-bearing solutions in these cavities, before the crystallization of the heavy mineral inclusions, held dissolved not only much larger quantities of mineral substances than can be taken up by water at ordinary temperatures, but also a substance like ferric oxide which is entirely insoluble under ordinary cool conditions.
(5) The association of the ores with minerals carrying fluorine and boron, with many silicate minerals, such as garnet, amphiboles, pyroxenes, mica (sericite) and others, and with other minerals which are known to be characteristic developments within or near igneous masses and which are not known to form under weathering agencies at the surface. Various characteristic groupings of these associated minerals are noted. In limestone much of the mass may be replaced by garnet and other silicates in a matrix of quartz. In igneous rock the ore-bearing solutions may have altered the wall rock to a dense mixture of quartz, sericite, and chlorite. Where sericite is dominant, the alteration is called sericitic alteration. Where chlorite is important, it is sometimes called chloritic or "propylitic" alteration. The chloritic phases are usually farther from the ore deposit than the sericitic phases, indicating less intense and probably cooler conditions of deposition. Locally other minerals are associated with the ores, as, for instance, in the Goldfield district of Nevada (p. 230), where alunite replaces the igneous rock. Alunite is a potassium-aluminum sulphate, which differs from sericite in that sulphur takes the place of silicon. In the quartzites of the lead-silver mines of the Coeur d'Alene district of Idaho (p. 212), siderite or iron carbonate is a characteristic gangue material replacing the wall rock.
Quartz in some cases, as noted above, gives evidence of high temperature origin and therefore of igneous association. Jasperoid quartz, as well illustrated in the Tintic district of Utah (p. 235), may show texture and crystallization suggestive of deposition from colloidal solution,—a process which can occur under both cold and hot conditions, but which is believed to be accelerated by heat.
Certain minerals, such as magnetite, ilmenite, spinel, corundum, etc., are often found as primary segregations within the mass of igneous rock. These and other minerals, including minerals of tin and tungsten, monazite, tourmaline, rutile, and various precious stones, are characteristically developed in pegmatites, which are known to be igneous rocks, crystallized in the later stages of igneous intrusion. When, therefore, such minerals are found in other ore deposits an igneous source is a plausible inference. For instance, in the copper veins of Butte, Montana (p. 201), are found cassiterite (tin oxide) and tungsten minerals. Their presence, therefore, adds another item to the evidence of a hot-water source from below.
(6) The occasional existence of hot springs in the vicinity of these ore deposits. Where hot springs are of recent age they may suggest by their heat, steady flow, and mineral content, that they are originating from emanations from the still cooling magmas. In the Tonopah camp (p. 236), cold and hot springs exist side by side, exhibiting such contrasts as to suggest that some are due to ordinary circulation from the surface and that others may have a deep source below in the cooling igneous rocks. This evidence is not conclusive. Hot springs in general fail to show evidence of ore deposition on any scale approximating that which must have been involved in the formation of this class of ore bodies. Much has been made of the slight amounts of metallic minerals found in a few hot springs, but the mineral content is small and the conclusion by no means certain that the waters are primary waters from the cooling of igneous rocks below.
In this connection the mercury deposits of California (p. 259), contribute a unique line of evidence. In areas of recent lavas, mercuric sulphide (cinnabar) is actually being deposited from hot springs of supposed magmatic origin, the waters of which carry sodium carbonate, sodium sulphide, and hydrogen sulphide,—a chemical combination known experimentally to dissolve mercury sulphide. The oxidation and neutralization of these hot-spring solutions near the surface throws out the mercury sulphide. At the same time the sulphuric acid thus formed extensively leaches and bleaches the surrounding rocks. Such bleaching is common about mercury deposits. When it is remembered that the mercury deposits contain minor amounts of gold and silver and sulphides of other metals; that they are closely associated with gold and silver deposits; and further that such gold, silver, and other sulphide deposits often contain minor amounts of mercury,—it is easy to assume the possibility that these minerals may likewise have had their origin in hot solutions from below. The presence of mercury in a deposit then becomes suggestive of hot-water conditions.
(7) Ores sometimes occur in inverted troughs indicating lodgment by solutions from below, as, for instance, in the saddle-reef gold ores of Nova Scotia and Australia, and in certain copper ores of the Jerome camp of Arizona (p. 204.) This occurrence does not indicate whether the solutions were hot or cold, magmatic or meteoric, but in connection with other evidences has sometimes been regarded as significant of a magmatic source beneath.
Perhaps no one of these lines of evidence is conclusive; but together they make a strong case for the conclusion that the solutions which deposited the ores of this class were hot, came from deep sources, and were probably primary solutions given off by cooling magmas.
The conclusion that some ores are derived from igneous sources, based on evidence of the kind above outlined, does not mean necessarily that the ore is derived from the immediately adjacent part of the cooling magma. In fact the evidence is decisive, in perhaps the majority of cases, that the source of the mineral solutions was somewhat below; that these solutions may have originated in the same melting-pot with the magma, but that they came up independently and a little later,—perhaps along the same channels, perhaps along others.
It is hardly safe, with existing knowledge, to apply the above conclusion to all ore deposits with igneous associations, or in any case to eliminate entirely another agency,—namely, ground-waters of surface or meteoric origin, which are now present and may be presumed often to have been present in the rocks into which the ores were introduced. Such waters may have been heated and started in vigorous circulation by the introduction of igneous masses, and thereby may have been enabled to effectively search out and segregate minutely disseminated ore particles from wide areas. This has been suggested as a probability for the Kennecott copper ores of Alaska (p. 200) and for the copper ores of Ely, Nevada. In the Goldfield camp (p. 230) the ores are closely associated with alunite in such a manner as to suggest a common origin. It has been found difficult to explain the presence of the alunite except through the agency of surface oxidizing waters acting on hydrogen sulphide coming from below.
In the early days of economic geology there was relatively more emphasis on the possible effectiveness of ground-waters in concentrating ores of this type. With the recognition of evidence of a deeper source related to magmas, the emphasis has swung rapidly to the other extreme. While the evidence is sound that the magmatic process has been an important one, it is difficult to see how and to just what extent this process may have been related to the action of ground-waters,—which were probably present in a heated condition near the contact. It may never be possible to discriminate closely between these two agencies. It seems likely that at some stages the two were so intimately associated that the net result of deposition cannot be specifically assigned either to one or to the other.