Gold was undoubtedly the first metal to be used by primitive man; for, occurring as it did in the stream beds, its bright color quickly attracted the eye, and it was so soft, that it was easily worked into various shapes, which, because they did not tarnish, became permanent ornaments. The metal is associated with the very earliest civilizations, being found in such ancient tombs as those at Kertsch in Crimea and in northern Africa and Asia Minor. It was used in the cloisonné work of Egypt 3000 yearsB.C.In America the Indians, especially to the south, were using it long before the continent was discovered.
Of all the metals gold is the most malleable, and its ductility is remarkable, for a piece of a grain’s weight (less than the size of a pin head) can be drawn out into a wire 500 feet long; andit can be beaten into a thin leaf as thin as ¹/₂₅₀₀₀₀ of an inch in thickness, and thus a bit, weighing only a grain, can thus be spread over 56 square inches.
It forms very few compounds, but has a considerable tendency to make alloys (i.e., mixtures with other metals without the resulting compound losing its metallic character). In Nature gold is never entirely pure, but is an alloy, usually with silver, there being from a fraction of 1% up to 30% of the silver with the gold, the more silver in the alloy, the paler the color of the gold. Australian gold is the purest, having but about .3% of silver in it, while Californian gold has around 10% and Hungarian gold runs as high as 30% of silver. Another alloy fairly abundant in Nature is that with tellurium, such ascalaverite(AuTe₂) which is a pale brassy yellow, similar to pyrite, but with the hardness of but 2.5. Another combination includes gold, silver and tellurium,sylvanite, (AuAgTe₄) a silvery white mineral with a hardness of but 2. Such combinations are known as tellurides and the calaverite is mined as a source of gold at Cripple Creek, Colo., while the sylvanite is one of the important ores of gold in South Africa. Occasionally gold is also found alloyed with platinum, copper, iron, etc. Jewelers make several alloys, “red gold” being 3 parts gold and 1 of copper, “green gold” being the same proportions of gold and silver, and “blue gold” being the combination of gold and iron. Our gold coins are alloys, nine parts gold and one of copper, to give them greater durability. Most ofthe gold recovered from nature is found native,i.e., the pure metal, or with some alloy.
Usually non-crystalline, but occasionally showing cube or octahedral faces of the isometric system; hardness 2.5; specific gravity 19.3; color golden yellow; luster metallic; opaque.
Gold is mostly found as the metal and is readily recognized by its color, considerable weight, hardness, malleability, and the fact that it does not tarnish. It usually occurs in quartz veins in fine to thick threads, scales or grains, and occasionally in larger masses termed “nuggets.” It is insoluble in most liquids so that when weathered from its original sites, it was often washed down into stream beds, to be found later in the sands or gravels, or even in the sea beaches. When thus found it is termed “placer gold,” and its recovery is placer mining. Most of the original discoveries of gold have been in these placer deposits; and from them it has been traced back to the ledges from which it originally weathered. In the placer deposits the size of the particles varies from fine “dust” up to large nuggets, the largest found in California weighing 161 pounds; but the largest one found in the world was the “Welcome Nugget,” found in Australia, and weighing 248 pounds. When gold was discovered in California in 1848, this became the chief source for the world, but later this distinction went to Australia, and now belongs to South Africa, which today yields over half the annual supply.
The ultimate source of gold is from the lighter colored igneous rocks, like granites, syenites, and diorites, throughout which it is diffused in quantities too small to be either visible or worth while to extract. It becomes available only when it has been dissolved out by percolating waters and segregated in fissures or veins, either in or leading from these igneous rocks. Generally this transfer of gold has taken place when the rocks were at high temperatures, and by the aid of water (and perhaps other solvents) which was also at high temperatures. The presence of gold in sandstones, limestones, etc., is secondary, as is also its presence in sea water, in which there is reported to be nearly a grain (about five cents worth) in every ton of water. Beside the direct recovery of gold from gold mining, a great deal is obtained from its association with iron, copper, silver, lead and zinc sulphides, in which it is included in particles too fine to be visible, but in quantities large enough to be separated from the other metals after they are smelted.
In the United States gold is found in the Cordilleran region from California to Alaska, in Colorado, Nevada, Arizona, Utah, the Black Hills of South Dakota, and in small quantities in the metamorphosed slates of North and South Carolina, Georgia, and in Nova Scotia.
Though much commoner than gold, silver did not attract the eye of man as early, probably because it tarnishes when exposed to air or any other agent having sulphur compounds in it,and a black film of silver sulphide covers the surface. Its first use was for ornaments, and some of these found in the ruins of ancient Troy indicate its use as early as 2500B.C.A thousand years later it was being used to make basins, vases and other vessels.
Silver is next to gold in malleability and ductility, so that a grain of silver can be drawn out into a wire 400 feet long, or beaten into leaves ¹/₁₀₀₀₀₀ of an inch in thickness. As a conductor of electricity it is unsurpassed, being rated at 100% while copper rates 93%. Silver is also like gold in the freedom with which it alloys with other metals, such as gold, copper, iron, platinum, etc. All our silver coins, tableware, etc., have some copper alloyed with the silver to give it greater hardness and durability.
Unlike gold, silver freely enters into compounds with the non-metals, which is the reason that it is not found primarily in its native state, but usually as a sulphide. Its ultimate source is in the igneous rocks, few granites or lavas, on analysis, failing to show at least traces of silver. Before it is available as an ore, or mineral, it has been dissolved from the original magma, and segregated in fissures or veins, along with such minerals, as quartz, fluorite, calcite, etc. This seems to have taken place while the igneous rocks were still hot, and by the agency of vapors and liquids which were also hot. The presence of silver in sedimentary and metamorphic rocks, or even in sea water, is secondary.
The primary deposition of silver is usually in the form of sulphides, the commoner of whichare, argentite or silver sulphide, pyrargyrite or silver and antimony sulphide, and prousite, or silver and arsenic sulphide. Its occurrence as native silver, or the chloride, cerargyrite, is secondary and due to the reactions which have taken place when sulphide deposits have been subjected to weathering agents.
The United States produces about 25% of the world’s supply, Mexico some 35%. It is especially found along the Cordilleran ranges of both North and South America.
Usually non-crystalline, but occasionally showing cube or octahedron faces of the isometric system; hardness 2.5; specific gravity 10.5; color silvery white; luster metallic; opaque.
When found in its native state silver is usually in wirey, flakey, or mossy masses; but sometimes masses of considerable size occur, the most famous being an 800 pound nugget found in Peru, and another of 500 pounds weight found at Konsberg, Norway, and now preserved in Copenhagen. When exposed to the air the surface soon tarnishes and takes on a black color which must be scraped off to see the real color.
Like gold, silver is usually found associated with other metals, like iron, copper, lead and zinc; and much of the silver recovered is obtained in connection with the mining, especially of copper and lead. Some lead ores have so much silver in them that they are better worth mining for the silver; galena, for instance, under such circumstances being termed argentiferousgalena. Native silver is a secondary mineral, having been formed by the reduction of some one of its sulphides by water, carrying various elements which had a greater affinity for the sulphur.
Silver is found along with copper in the Lake Superior region, and in Idaho, Nevada, and California.
Usually in irregular masses, but sometimes in cubes; hardness 2.5; specific gravity 7.3; color and streak lead gray; luster metallic; opaque on thin edges.
Argentite, the simple sulphide of silver, is the chief source from which silver is obtained. It looks like galena, and has the same hardness, streak and specific gravity, but can be distinguished by the galena having a very perfect cubic cleavage while the argentite has no cleavage. Argentite is easily cut with a knife (sectile). It is usually found in irregular masses, but sometimes in cubes which make very choice cabinet specimens; and is associated with such other minerals as galena, sphalerite, chalcopyrite, pyrite, fluorite, quartz, and calcite.
It occurs in fissures and veins all through the Cordilleran regions, especially in California, Colorado, Nevada (Comstock Lode), Arizona (Silver King Mine) and about the shores of Lake Superior.
Usually occurs in irregular masses; hardness 2.5; specific gravity 5.8; color dark red to black; streak purplish red; luster metallic to adamantine; translucent on thin edges.
Pyrargyrite, the sulphide of silver and antimony, is distinguished by its dark red color and the purplish streak. It may look like prousite, but is easily distinguished from the latter which has a scarlet streak. It also at times looks like hematite and cinnabar, but the hematite has a hardness of 6, and the latter has the bright red color throughout, while pyrargyrite turns black when exposed to the light, so that the characteristic red color will be seen only on fresh surfaces. The characteristic red color can only be kept on the mineral if it is constantly protected from the light.
Sometimes pyrargyrite occurs in crystals and these belong to the hexagonal system, and are prisms with low faces on the ends, as onplate 7, and the mineral is peculiar in that the faces on the opposite ends are unlike.
Pyrargyrite is found mostly in fissures and veins of quartz, fluorite, calcite, etc., and associated with pyrite, chalcopyrite, galena, etc. It is fairly common in Colorado in Gunnison and Ouray counties, in Nevada, New Mexico, Arizona, etc.
Usually occurs in irregular masses; hardness 2.5; specific gravity 5.6; color scarlet to vermilion; streak the same; luster adamantine; transparent on thin edges.
In general this mineral is very like pyrargyrite, but has the scarlet color and streak which are entirely characteristic. It is likely to have the surface tarnished black, which happens on exposureto light, so that it is essential to be sure that fresh surfaces are being examined. Occasionally it is found in crystals, of the same type as the preceding mineral. It is generally found associated with pyrargyrite.
Usually found in irregular masses or incrustations; hardness 1 to 1½; specific gravity 5.5; color pearly gray, grayish green to colorless, but turning violet brown on exposure to light; luster resinous; transparent on thin edges.
This mineral is usually found in thin seams or waxy incrustations, but it may occur in crystals in which case they are cubes. It is very soft and easily cut with a knife, which with its tendency to turn violet-brown on exposure to light, makes it easy to identify. Cerargyrite is a secondary mineral, resulting from the action of chlorine-bearing water on some one of the sulphides of silver. It is found in the upper portions of mines, especially those in arid regions.
After gold the next metal to be utilized was copper. About 4000B.C.our early forefathers found that by heating certain rocks, they obtained a metal which could be pounded, ground and carved into useful shapes. Curiously enough the rocks which had the copper also had some tin in them, so that this first-found copper was not pure, but had from five to ten per cent of tin in it, making the resulting metal harder, andwhat we call bronze. It was some thousands of years later before they distinguished the copper as a pure metal, but it worked and made good tools. The newly found metal was not as ornamental as gold; but, because it could be made into tools, it had a tremendous influence on man’s development. As the bronze tools began to take the place of the stone implements, the “Age of Bronze” was ushered in. In America the Indians in the Lake Superior region found native copper weathered out of the rocks and later mined it, and they too pounded it into knives, axes, needles, and ornaments, but probably never learned to melt it and mold their tools. At any rate they were not as far advanced in using this metal when Columbus landed as were the southern Europeans 6500 years earlier. Since the use of iron became general, copper has not held such a dominant place, but it still is “the red metal” which holds the second most important place.
It is malleable and ductile, though not equal to gold or silver in these respects. It is a good conductor of electricity and a very large amount of copper is used in electrical manufacture, roofing, wire, etc. It alloys with other metals; ten parts copper and one of tin being bronze, ten of copper and one of zinc is brass, and copper with aluminum is aluminum bronze.
Like silver and gold, copper is widely diffused through the igneous rocks, but before it is available, it must be leached out by solvents and concentrated in veins, fissures, or definite parts of the lavas or granites. The primary ores arethose which, while the igneous rock was still hot, were carried by hot vapors and liquids into the fissures and there deposited, mostly as sulphides. There is a long list of these, but in this country, the following are the commoner ones; chalcocite the sulphide of copper, chalcopyrite the sulphide of copper and iron, bornite another combination of copper, iron and sulphur, and tetrahedrite copper and antimony sulphide. When these primary ores are near enough to the surface to come in contact with waters carrying oxygen, carbon dioxide or silica in solution, they may give up their sulphur and take some one of these new elements and we have such forms as cuprite, the oxide of copper, malachite and azurite, carbonates of copper, or chrysocolla, the silicate of copper. Native copper is also a secondary deposit laid down in its present state by a combination of circumstances which deprived it of its original sulphur. In general copper mining can not be profitably carried on for ores with anything less than a half of one percent in them; and the use of such low grade ores has only been possible for a few years, as the result of inventing most delicate processes in the smelting.
The United States produces about a quarter of the world’s supply of copper, with Chile ranking second with about 17%.
Usually in irregular masses; hardness 2.5; specific gravity 8.9; color copper red; luster metallic; opaque. Native copper, easily determined by its colorand hardness, is generally found in irregular grains, sheets, or masses, on which may sometimes be detected traces of a cube or an octahedral face, showing that it belongs to the isometric system. The most famous locality is the Upper Peninsula of Michigan which may be taken as typical. Here, long before it was known historically, the Indians found and dug out copper to make knives, awls, and ornaments.
In this region, beds of lava alternate with sandstones and conglomerates. The copper was originally in the lavas, but has been dissolved out, and now fills cracks and gas cavities in the lavas, and also the spaces between the pebbles of the conglomerate. This locality has been very famous both because of the quantity mined, and also because of the strikingly large masses sometimes found. Today but little of the ore runs above 2 percent copper, and it is mined if it has as little as ½ of one percent.
While nowhere near as abundant, native copper occurs in the same way in cavities and cracks in the trap rocks of New Jersey, and along the south shore of the Bay of Fundy. It is also known from Oregon, the White River region of Alaska, and in Arctic Canada.
Occurs in crystals of irregular masses; hardness 4; specific gravity 4.2; color bronze yellow; streak greenish black; luster metallic; opaque on thin edges.
Chalcopyrite resembles pyrite, but its color is a more golden yellow, and its surfacetarnishes with iridescent colors. Then too the hardness of chalcopyrite is but 4 as compared with 6 for pyrite. When in crystals this mineral belongs to the tetrahedral system as the c axis is but .985 in length as compared with I for the two other axes. This difference is so little that, to the eye, the octahedron appears to belong to the isometric system. Chalcopyrite occurs in octahedrons and tetrahedrons (as onplate 8), the latter being the form where but half of the octahedral faces are developed. However by far the most frequent mode of occurrence is in irregular masses.
This is the most important primary ore of copper, and is widely distributed, being found either in lavas, or in veins, or in fissures connected with igneous rocks. Apparently the deposits were made, either at the time of eruptive disturbances or shortly afterward, from vapors or hot solutions carrying the copper sulphides (and other sulphides) from the molten igneous rocks. Chalcopyrite is usually associated with pyrite, galena, sphalerite and chalcocite, as well as quartz, fluorite and calcite. It is found in all the New England States, in New York, New Jersey, Pennsylvania, Maryland, Virginia, North Carolina, Tennessee, Missouri, and all the Rocky Mountain and Pacific Coast States.
Occurs in granular or compact masses; hardness 3; specific gravity, 5; color bronze-brown with a bluish tarnish; streak gray-black; luster metallic; opaque on thin edges.
Bornite is also known as erubescite, blushing ore, variegated copper, peacock copper, etc., all of which names refer to the highly iridescent tarnish which fresh faces soon take on when exposed to the air. Though usually in masses, it is sometimes found in rough cubes of the isometric system. In this country it is not abundant enough to be used as an ore, but is likely to be found with other ores like chalcopyrite or chalcocite. In the east it has been found at Bristol, Conn., and near Wilkesbarre, Penn., while in the west it may be expected to occur wherever other sulphide minerals of copper are found.
Occurs in fine grained compact masses; hardness 2.5; specific gravity 5.7; color dark leaden gray; streak black; luster metallic; opaque on thin edges.
Chalcocite is one of the important ores of copper, especially in Arizona and the Butte District of Montana. It resembles argentite in color and general appearance, but is readily distinguished by being brittle and having a tendency to tarnish to bluish or greenish colors on fresh surfaces. Occasionally it occurs in crystals which are in the orthorhombic system; but the edges of the prism are so beveled that there are six sides and the prism resembles a hexagonal prism (seepage 16).
In the Butte, Mont., district, the most important copper region in the United States, fully 50% of the ore is chalcocite, which is a derivative of the originally deposited chalcopyrite, the latterhaving lost its iron. In the veins of this district chalcopyrite, bournite, tetrahedrite, and several other copper minerals not described in this book, occur all together, and with them also gold, silver and arsenic minerals. The gold amounts to about 2¼ cents per pound of copper, and the silver is in somewhat less quantity. These veins were first opened to get the silver ores, which were the more important ones down to a depth of 200 to 400 feet. Below these depths the copper became much more important. It was the weathering which had removed a large part of the copper minerals in the upper levels of the veins, but had left a large part of the silver. Chalcocite is also important in most of the Utah and Arizona mines.
In the east it has been found at Bristol, Simsbury and Cheshire, Conn., and in the west it is found in all the Cordilleran States.
Occurs in irregular masses and in tetrahedrons of the isometric system; hardness 3.5; specific gravity 4.7; streak dark brown; luster metallic; opaque on thin edges.
In its crystalline form the tetrahedrite occurs in tetrahedrons, which generally have faces formed by beveling the edges and by cutting the corners, as in the two figures ofplate 10. Chalcopyrite may also occur in tetrahedrons, but its golden yellow color is entirely different from the gray-black of the tetrahedrite. When in masses the hardness and the streak which is dark brown, are very characteristic.
In England and Bolivia tetrahedrite is an important ore of copper, but in this country it is simply a copper mineral which is widely distributed, and associated with most of the mining enterprises, but is in no case the important ore. It has been found sparingly through the New England States, at the Kellogg Mines in Arkansas, and abundantly in Colorado, Montana, Utah, Arizona, Nevada and New Mexico.
Occurs in isometric cubes, octahedrons, and dodecahedrons, or in masses; hardness 3.5; specific gravity 6; color dark brownish-red; streak brownish-red; luster metallic; translucent on thin edges.
When in crystals cuprite is easily determined, but when in masses its fresh surfaces may suggest prousite, but the streak and hardness are quite different in the two cases. Sometimes its color suggests hematite, but the latter has the hardness of 6. When found it is often coated with a thin film of green, which is malachite.
Except when found as native copper, the ore which contains the greatest percentage of copper is cuprite with 88.8% of copper. It is likely to occur in any of the deposits of copper ore, where they are in arid climates and above the level of the underground water, and is very frequently associated with malachite and azurite. In the Bisbee, Arizona, district cuprite is one of the important ores.
Besides the normal occurrence described above, cuprite may be found in two other varieties;one where the crystals have grown side by side and so only the ends have been free for continuous additions of the mineral, which has resulted in a fibrous mass known as “plush copper ore” or chalcotrichite; the other an earthy mixture of limonite and cuprite, which is brick red in color, and termed “tile ore.”
Cuprite is found sparingly in New England, more abundantly at such places as Summerville and Flemington, N. J., Cornwall, Penn., in the Lake Superior region, and fairly abundantly in the Cordilleran States.
Usually occurs in nodular or incrusting masses; hardness 3.5; specific gravity 4; color green; streak a lighter green; luster adamantine, silky or dull; translucent on thin edges.
The vivid green of malachite is usually enough to determine it at once, but one may be sure by trying a drop of acid on it, in which case it effervesces as is characteristic of so many carbonates, but this is the only carbonate which is vivid green. Generally the malachite is in irregular masses, but crystals are occasionally found. These are extremely small and needle-like, and belong to the monoclinic system. In the Ural Mountains there is a locality where these crystals grow in fibrous masses, usually radiating from the center. Malachite in such nodules has a silky luster. These rare nodules have furnished the rulers of Russia with a unique and much prized material for making royal gifts. In European museums and palaces one findsmany objects carved from this form of malachite, and marked as gifts of the czars of Russia.
In the United States malachite is widely distributed, appearing as green streaks and stains where copper minerals have been exposed to the air. It is the green tarnish which appears on bronze and copper when exposed to the weather. It is found in large quantities in New Jersey, Pennsylvania, Wisconsin, Nevada, Arizona, Utah, New Mexico, etc. The Bisbee mine in Arizona is the place that has furnished museums with so many of the handsome specimens of malachite associated with azurite. These are the most striking specimens for the vividness of their colors that appear in any collections.
Malachite has been known since about 4000B.C., the Egyptians having mines where they obtained it between the Suez and Mt. Sinai. In those early days it was particularly a child’s charm, protecting the wearer from evil spirits. It is still used as a stone of lesser value in making some sorts of jewelry.
Occurs as short prismatic or tabular crystals of the monoclinic system; hardness 4; specific gravity 3.8; color azure blue; streak lighter blue; luster vitreous; translucent on thin edges.
Azurite is another very striking mineral fully characterized by its color and streak. Like malachite it effervesces in acid. It is very near to malachite in composition, and by increasing its water content, can and freely does change to the green mineral; so that few specimens ofazurite are without traces of malachite. It is found in the same places as malachite, but is not as abundant in the east.
Azurite with the accompanying malachite is cut and polished to make semi-precious stones for some forms of jewelry.
Never occurs in crystals, but in seams and incrustations; hardness 2-4; specific gravity 2.1; color bluish-green; streak white; luster vitreous; translucent on thin edges.
This rather rare mineral often appears in opal- or enamel-like incrustations, and its color is variable ranging from the typical bluish-green to sky-blue or even turquoise blue. This is a mineral resulting from the action of silica bearing waters, coming in contact with most any of the copper minerals, and is found accompanying cuprite, malachite, azurite, etc. It is never in large enough quantities to be used as an ore, but its striking color attracts attention and it can be found fairly frequently, especially in the west.
Pure iron is a chemical curiosity which looks very much like silver. As obtained from its ores, or as it occurs in Nature, iron always has some impurities with it, such as carbon, silicon, sulphur and phosphorus, and these are highest in the crudest iron such as “pig-iron.” Its malleability and ductility are only a little less than for gold and silver, and so it has a wide range of qualities for use by man. It is only rarely found native in minute grains in some of the dark lavas. Thereis however one remarkable exception to this statement, in that on Disco Island, Greenland, there is a basaltic rock, from which are weathered great boulders of native iron up to 20 tons in weight. This iron is very like that occurring in meteorites, and probably came from great depths in the earth’s interior. The specific gravity of iron is 7.8. It makes up around 5% of the crust of the earth, and probably occurs in much larger percentages in the interior of the earth.
Iron was discovered by man later than gold or silver or copper, about 1000B.C.; but once found it was so much more abundant than any of these that it soon dominated over copper, and from Roman times to the present has been the basis of progress in civilization, and these times are well called “the iron age.”
Iron unites freely with the non-metals, and occurs as sulphides, oxides, carbonates, etc., and is also present as a secondary metal in that great group of minerals known as the silicates (seepage 97). It alloys with a wide range of other metals, every combination altering the properties of the iron, and thus making it useful in a still greater range of manufacture. The introduction of ¼ to 2½% of carbon into iron makes steel, which is harder (in proportion to the amount of carbon) and stronger than the pure iron.
Iron compounds are among the most numerous and important of the colors in Nature’s paint box, limonite furnishing the browns which color the soil and so many of the rocks, hematite giving the red color to other abundant rocks, and magnetite often coloring igneous rocks black,while the chlorophyll which gives the green color to plants is an iron compound, as is also the hemoglobin which gives the red to our blood.
Iron is present in all igneous rocks, and secondarily in the sedimentary and metamorphic rocks. It is soluble in water, and so is being constantly transferred from place to place, and changes from one compound to another, according to the circumstances in which it is placed.
The primary forms are pyrite, magnetite and the silicates. When in weathered rocks the iron is changed to limonite, siderite or hydrated silicates. Hematite is an intermediate oxide from which the water contained in limonite has been driven off by moderate heat or bacterial action.
Never crystalline, occurs in mammillary, botryoidal and stalactitic forms, or in fibrous, compact, oolitic, nodular or earthly masses; hardness 5.5; specific gravity 3.8; color yellow-brown to black; streak yellow-brown; luster metallic to dull; opaque.
Limonite is a very common mineral, the color, streak and hardness identifying it readily. Iron rust is its most familiar form. When powdered it is the ochre yellow used in paints. Being so universally distributed, it is to be expected it will occur in a variety of ways. First, there is the fibrous type found lining cavities, in geodes, or hanging in stalactites in caves. This has a silky luster, an opalescent, glazed or black surface, and is in mammillated or botryoidal masses. Second, it may occur in compact masses in veins, where it was deposited by waters; which, circulatingthrough the adjacent rocks, gathered it from the rocks, and, on reaching the open seams, gave it up again. Third, it may occur in beds on the bottom of ponds, where it was deposited by waters which gathered it as they flowed over the surface of the country rocks. Measurements in Sweden show that it may accumulate in such places as much as six inches in the course of twenty years. In ponds and swamps, the decaying vegetation forms organic compounds, which cause the precipitation of the iron from the water, as it is brought in by the streams. This sort of iron in the bottom of ponds or swamps is also known as “bog iron.” Another form in which limonite may occur in ponds, lakes, or even the sea, is in oolitic masses. In this case the iron forms in tiny balls, with perhaps a grain of sand at the center, and one coat of iron after another formed around it, like the layers of an onion. If the resulting balls are tiny this is called oolitic (like fish eggs), but if the balls are larger it is pisolitic (like peas). Bacteria probably have a good deal to do with the precipitation of limonite in this manner. Fourth, limonite occurs in earthy masses, usually mixed with impurities like clay and sand, which are the residue left behind, where limestones have been dissolved by weathering. The fifth mode of occurrence is known as gossan, or “the iron hat,” which is a mass of limonite capping a vein of some sulphide mineral, like pyrite, chalcopyrite or pyrrhotite, which has been exposed to weathering; and in these minerals the sulphur has been removed, leaving a mass of limonite over the vein. This isparticularly common in the west. Limonite is quite easily fusible and so was probably the first ore from which early man extracted iron.
Limonite is iron oxide, with 3 molecules of water of crystallization (or constitution) associated with every 2 molecules of the oxide. If limonite is moderately heated the water is driven out and the resulting compound is hematite, the same oxide, but without the water. In this case and many other similar cases, as gypsum, opal, etc., we have two or more minerals resulting from the presence or absence of water in the mineral. The water molecules have a definite place in the arrangement of molecules which determines the structure of the mineral. Sometimes the water is driven out at a temperature around 212 F., in which case it is called, water of crystallization, but in other cases as gypsum, a considerably higher temperature is required to drive out the water, and then it is called, water of constitution. In all cases the removal of the water changes the arrangement of molecules and a new mineral results, with characteristics of its own.
In this case limonite is only one of a series of minerals which have the Fe₂O₃ molecule as a basis, and that incorporate more or less water into their molecular construction as follows:
Of these goethite is crystalline, the others non-crystalline. They may occur pure or in all sorts of mixtures, the mixtures usually being lumped under limonite. The limonite is far the commonest of the series, goethite is fairly common, but the others are rare as pure minerals.
Limonite is found in all parts of all states and in every country. Though so common, it is by no means an important source of iron today, only about one percent of the iron mined in this country coming from this source, though in Germany, Sweden and Scotland it is relatively much more important.
Occurs in lustrous brown to black orthorhombic prisms, usually terminated by low pyramids; hardness 5; specific gravity 4; color brown to black; streak brownish-yellow; luster imperfect adamantine; opaque.
Goethite, named for the poet Goethe, who was interested in mineralogy, is much less abundant than limonite or hematite, but occurs with them, when they are in veins. Its usual form is an orthorhombic prism with the edges beveled, and a low pyramid on either end. The crystals usually grow in clusters, making a fibrous mass, often radiated, in which case it is known as “needle iron stone”; or the prisms may be so short as to be almost scales; when, because of the yellowish-red color, it is called “ruby mica”. It is found in many states, including Connecticut, Michigan, Colorado, etc.
Occurs in compact, mammillary, botryoidal, or stalactitic masses of dark red to black color, or in earthy masses of bright to dark red; hardness 6; specific gravity 5.2; color ochre red to black; streak cherry red to dark red; luster metallic, vitreous, or dull; opaque on thin edges.
Hematite is readily distinguished from other red minerals by its hardness and streak. It may occur in crystals, which belong to the hexagonal system, and are usually hemihedral forms of the double pyramid, or rhombohedrons. These rhombohedrons usually have the edges beveled, as inPl. 13, A; or are tabular in form as a result of the beveling of two of the opposite edges to such an extent that a form likePl. 13B results. However the usual occurrence is in non-crystalline masses, which represent transformations from limonite by the loss of water of crystallization on the part of the limonite. In such cases we have fibrous, oolitic or compact masses, according to the form in which the limonite occurred. The transformation from limonite into hematite involves some heat to drive out the water of crystallization, but nothing like what is involved in metamorphism.
Hematite is the source of 90% of the iron mined in this country. Part of it comes from the famous Clinton iron ore, a layer a foot or more in thickness; starting in New York State, and extending all down the Appalachian Mountains to Alabama, where it is ten or more feet thick and the basis of the Birmingham iron industries. Then there are tremendous depositsof earthy to compact hematite, probably derived from limonite, around the west end of Lake Superior. This latter region yields today around 75% of the iron for this country.
Loose earthy masses of hematite are often known as “ochre red,” and were used by the Indians for war paint. Today the same sort of material is obtained by powdering hematite and using it for red paint. The red color in great stretches of rock is due to the presence of small amounts of hematite, acting as cementing material. The red of the ruby, garnet, spinel, and the pink of feldspars and calcite are due to traces of hematite.
This mineral is very common and found in every state.
Occurs in masses or in isometric octahedrons or dodecahedrons; hardness 6; specific gravity 5.8; color black; streak black; luster metallic; opaque on thin edges.
Magnetite is another important ore of iron, and is peculiar in being strongly magnetic; its name being derived, according to Pliny, from that of the shepherd Magnes, who found his iron pointed staff attracted by the mineral when he was wandering on Mount Ida. This magnetic property has been repeatedly used to locate beds of magnetite, and is very helpful in separating magnetite from the “black sands,” of which it so often forms a part. These sands however generally have magnetite with so much titanium in it that they are unfit for smelting.
Magnetite is found in association with igneous or metamorphic rocks, and often represents limonite or hematite which has been altered as the result of high temperatures. Some of it, in the igneous rocks especially, was undoubtedly in the molten magma and has crystallized out from the magma while it was still hot. It is the form of iron always indicative of former high temperatures. It is an ore mineral for about 3% of the iron in this country, but in Scandinavia and some other countries, it plays a leading role as the source of iron.
It is found in the Adirondack Mountains, in New Jersey, Pennsylvania, Arkansas, North Carolina, New Mexico, and California.
Occurs in fibrous botryoidal masses or rhombohedral crystals, sometimes with curved faces; hardness 3.5; specific gravity 3.8; color gray-brown; streak white; luster vitreous; translucent on thin edges.
Like hematite this mineral belongs to the hexagonal system, and crystallizes in hemihedral form, making the rhombohedron. Its faces are often curved, which is rare in minerals, only a few forms like this and dolomite having other than plane faces. When siderite crystals grow in clusters, the crowding often results in growth on one face only, making a mass of fibrous character, and in such cases the surface of the mass is botryoidal in contour. The mineral is likely to oxidize, losing its gray-brown color, and becoming limonite. In the UnitedStates it is scarcely ever used as an ore for iron, but in Germany and England a great deal of iron is smelted from this mineral.
It occurs in Massachusetts, Connecticut, New York, throughout the Appalachian Mountains, and also in Ohio.
Occurs as cubes, octahedrons and pyritohedrons, or in compact masses, scales or grains; hardness 6; specific gravity 5.1; color brassy yellow; streak greenish-black; luster metallic; opaque on thin edges.
This is one of the commonest of all minerals. It is found in all kinds of rocks, with all kinds of associations, in all parts of the world. Its crystals are isometric, and cubes and octahedrons are abundant. The pyritohedron is also a common form, and characteristic of this mineral. It is a hemihedral form derived from a 24-sided form,i.e.the cube with four faces on each side. On this 24-sided form each alternate face has developed and the others have disappeared, resulting in a 12-sided form, known as the pyritohedron, which differs from the dodecahedron in that each of its faces is five-sided instead of rhomboidal. When in crystals pyrite can not be easily confused with any other mineral; but when in masses it is often mistaken for gold, chalcopyrite, pyrrhotite or marcasite. From the first two, the color should be sufficient to distinguish it, for they are golden yellow. Pyrrhotite is bronze yellow, and marcasite is paler yellow. Then too in hardness pyrite ismuch harder than any of these minerals except marcasite. This last is the one which is most likely to cause real difficulty. Its lighter color, and the fact that it usually comes in fibrous masses are the best distinctions.
In spite of being so abundant pyrite is scarcely ever used as an ore for iron, because the sulphur makes the metal “short,” or brittle, and the sulphur is not easily gotten entirely out of the iron; but pyrite is used largely in the manufacture of sulphuric acid, so important to many of our industries.
Other sulphides are commonly mixed with pyrite, such as chalcopyrite, arsenopyrite, argentite, etc.; but the most important impurity is gold, which is often scattered through the pyrite in invisible particles, and sometimes in quantities enough to make it worth while to smelt it for the gold.
Pyrite is particularly the form in which the sulphur compounds of iron appear in rocks which have been highly heated, and is to be expected in metamorphic rocks and also igneous rocks, especially in fissures and veins leading from the igneous rocks. It may occur in sedimentary rocks, but in these last it is usually marcasite.
Occurs in orthorhombic crystals, usually grouped to make fibrous or radiating masses, or non-crystalline in masses; hardness 6; specific gravity 4.8; color pale brassy-yellow; streak greenish-gray; luster metallic; opaque on thin edges.
Marcasite has the same chemical composition,as pyrite, and looks like it, but is lighter colored and usually occurs in fibrous masses. It is the commoner form in limestones and shales, while pyrite is more likely to occur in igneous and metamorphic rocks. It seems probable that marcasite is due to a more hasty precipitation from cold solutions, while pyrite is deposited more slowly from hot solutions.
Isolated crystals of marcasite are rare; but, if formed, they belong to the orthorhombic system. Usually some form of twinning is present, and because of the multiple character of the twinning, marcasite crystals usually show a ragged outline, with reentrant angles. It is most abundant in radiated masses, which appear fibrous on the broken surfaces. It decomposes easily, taking oxygen from the air and forming, even in museum cases, a white efflorescence or “flower,” which is iron sulphate or melanterite. In moist air it takes water and decomposes to sulphuric acid which may change the surrounding limestone to gypsum. Marcasite is found wherever limestones and shales are the country rock.
Occurs in masses; hardness 4; specific gravity 4.6; color bronze; streak grayish-black; luster metallic; opaque on thin edges.
Tabular crystals are known, but are very rare. They belong to the hexagonal system. This form is easily distinguished from the other yellow minerals by being magnetic. It is by no means as abundant as the two preceding sulphides of iron, but does occur fairly frequently in veinsin igneous rocks, and less frequently in limestones, large quantities of sulphuric acid being made from a deposit in limestone at Ducktown, Tenn. It will be found in most states. When associated with nickel it is an important source for the latter mineral, as at Sudbury, Canada. Pyrrhotite is very like a substance found in meteorites, known as troilite.
After learning how to get iron from the rocks by rude smelting methods, the early peoples tried heating various rocks, and some time around 500B.C.stumbled upon lead, which is rather easily separated from its ores. This metal was used through Roman times to make pipes, gutters, etc.
Lead is a soft metal, fairly malleable, but with little ductility, and still less tensile strength. Though one of the commoner metals, it does not occur as pure metal in Nature. It is diffused in minute quantities through the igneous rocks, and also is found in the sedimentary rocks and in the sea water. Its minerals are few, galena, the sulphide of lead, being the commonest, and at the same time the form in which lead is primarily deposited. Galena may also represent a secondary deposition. The other minerals, cerrusite, anglesite, and pyromorphite are results of modification of the galena when it lies near enough to the surface to be acted on by weathering agents, like water and air. Lead minerals are usually associated with zinc minerals, there being but few places where the minerals of the one group occurwithout the other. Most lead when first smelted from its ore, contains a greater or less amount of silver in it, sometimes enough so that the lead ore is better worth working for the silver than for the lead.
Lead is used in making pipes, gutters, bullets, etc., and in its oxide forms in the manufacture of paints and glass. Eighty-three parts of lead with 17 parts of antimony make type metal. Lead and tin alloy to make solder. Lead and tin with small amounts of copper, zinc and antimony make pewter. The United States produce about 20% of the world’s supply of this metal.
Occurs in cubes or cleavable masses; hardness 2.5; specific gravity 7.5; color lead-gray; streak lead-gray; luster metallic; opaque.
While there is quite a group of lead-gray minerals, galena is easily identified by its cleavage, which is perfect in three directions parallel to the cube faces. Even a moderate blow of the hammer will shatter a mass of galena into small cubic pieces. The crystals often have the corners cut by octahedral faces, and occasionally the edges are beveled by dodecahedral faces. It is not uncommon to find crystals of large size, several inches across. If galena has 1 to 2% of bismuth as an impurity, curiously enough, the cleavage changes to octahedral, but this is a rare occurrence.
Galena may occur as a primary mineral in veins associated with igneous intrusions, or in irregularmasses in metamorphic rocks; but it is more often found in irregular masses in limestones, where the limestone has been dissolved, and the cavities thus formed, filled with secondary deposits of galena. It also occurs at the contact between igneous rocks and the adjacent rock, whatever this may be. Sometimes it is found in residual clays.
Among the most important lead deposits are the Cœur d’Alene district in Idaho, where galena with a high percentage of silver is mined; the Leadville, Colo., district where lead, silver and gold occur together in veins; the Joplin, Mo., district, where lead and zinc ores occur together in irregular masses in limestones; and the Wisconsin district of similar character.
When found galena is usually associated with sphalerite, argentite chalcopyrite, pyrite and calcite. It will be found in every state.
Occurs in fibrous or compact masses, or in orthorhombic crystals, usually on galena; hardness 3.5; specific gravity 6.5; colorless; streak white; luster adamantine; transparent on thin edges.
While the crystals of this mineral simulate hexagonal, they are actually orthorhombic, the simple form being an octahedron with two of its edges beveled, making double six-sided pyramids (seePl. 18A.) Usually prism faces are present. Twinning is common, both the simple contact sort, as shown onPlate 18B, and also the sort in which three crystals have grown through eachother, so as to make a six-rayed crystal. The considerable weight, and the fact that it effervesces in acid serve to identify cerrusite. When pure it is colorless, but impurities cause it to appear white, gray or grayish-black, and sometimes it has a tinge of blue or green.
It is likely to occur wherever galena is found, as a secondary mineral derived from the galena. In this country it is not used as an ore, for, as in the Leadville district, veins which have cerrusite near the surface change at moderate depths, and galena takes the place of the cerrusite. It is found all down the Appalachian Mountains, and in all the Cordilleran States. Especially fine specimens have come from the Cœur d’Alene district in Idaho.
Occurs in grains and masses, or in tabular and prismatic orthorhombic crystals; hardness 3; specific gravity 6.3; colorless; luster adamantine; transparent on thin edges.
Two modes of occurrence are characteristic, one in cavities in galena, the other in concentric layers around a nucleus of galena. In the former case fine crystals are developed, in the latter the mineral is in masses. The crystals look like those of barite, but are soluble in nitric acid while the barite is insoluble. Sometimes the crystals are prismatic with pyramidal faces instead of the tabular form.
It is found in the lead mines associated with galena, and in this country is not used as an ore for lead, but in Mexico and Australia it isabundant enough to be mined as an ore. Exposed to water which has carbon dioxide in it, and most surface waters have some, it readily changes to cerrusite. It is found in Missouri, Wisconsin, Kansas, Colorado, and Mexico.
Occurs in small barrel-shaped hexagonal crystals, and in fibrous or earthly masses; hardness 3.5; specific gravity 7; color green to brown; luster resinous; translucent on thin edges.
Pyromorphite is found in the upper levels of lead mines, and is formed by the decomposition of galena. Its green color (sometimes shading off toward brown), considerable weight and resinous luster, serve to distinguish this mineral. The crystal form is that of a simple hexagonal prism, with the ends truncated. It is found in Phœnixville, Penn., Missouri, Wisconsin, Colorado, New Mexico, etc.
Zinc and copper made the brass of early Roman times; but even then, zinc was not known as a separate metal, the brass being made by smelting rocks in which both zinc and copper occurred, the zinc never being isolated until much later. Some time in the later Roman times it seems to have been obtained separately, but then and all down through the Middle Ages zinc and bismuth were confused. Our earliest record of zinc being smelted, as we know it today, was about 1730 in England. In those earlierdays, the product, zinc, or bismuth, or both together, were known as “spelter,” and this name has clung to zinc in mining and commercial circles; so that today, if one looks for quotations in the newspaper, he often finds zinc under the head of spelter.
Zinc, like lead, is diffused in small quantities through all the igneous rocks. In places it is segregated in fissures or veins leading from the igneous rocks, along the contact between igneous rocks and either sedimentary or metamorphic rocks, in limestones where solution cavities have been formed and later filled with zinc minerals, and as a residue where limestones have been weathered away. In all these places it is closely associated with lead.
The sulphide, sphalerite, is the primary mineral, and the other minerals, like zincite, smithsonite, calamine, willemite, franklinite, etc., are secondary, resulting from modifications of the original sphalerite. In connection with zinc minerals the region of Franklin Furnace, N. J., is especially interesting, for at that place are found two large metamorphosed deposits containing a wide range of zinc minerals, several of which are not found anywhere else.
Zinc is soft and malleable, but is only slightly ductile, and has little tensile strength. It alloys with several metals, and in this form is most useful today; three parts of copper to one of zinc making brass; four or more parts of copper and one of zinc, making “gold foil”; copper and zinc (a little more zinc than copper) making “white metal”; three parts of copper to one ofzinc and one of nickel making German silver; etc. Zinc is also used in large quantities in galvanizing iron, sheets of iron being dipped into melted zinc and thus thinly coated. It is also used in batteries and a wide range of chemical industries.
Occurs in grains, in fibrous or layered masses, or in isometric crystals; hardness 3.5; specific gravity 4; color yellow-brown to almost black; streak light yellow to brownish; luster resinous to adamantine; translucent on thin edges.
When in crystals sphalerite occurs most commonly either in dodecahedrons or in tetrahedrons (hemihedral forms of the isometric octahedron). The cleavage is fairly good and parallel to the faces of the dodecahedron. The difficulty usually is to get large enough crystalline masses to see this cleavage clearly, but by examining the angles between the faces of cleavage pieces they will be found to be the same as those on a dodecahedron. When the mineral is pure, it has the color of resin, but sometimes it is reddish to red-brown, and then it is called “ruby zinc,” more often it is dark brown due to the presence of iron as an impurity. This is what the miners call “black-jack.” The presence of iron also tends to make the streak darker. The hardness, streak and cleavage will usually determine this mineral readily.
Sphalerite is the primary ore of zinc and is usually found in fissures and veins leading frommasses of igneous rocks, or along the surface of contact where igneous rocks like granite or lavas come against such metamorphic rocks as gneisses, schists, or crystalline limestones. In the region of Joplin, Mo., however, the sphalerite is of secondary character, having been gathered by waters circulating through the limestones, and deposited in them in irregular pockets. This Joplin district has produced more zinc than any other in the world. The United States annually produces about 25% of the world’s supply of this metal.
Sphalerite is always associated with galena, and such other minerals as argentite, pyrite, chalcopyrite, fluorite, quartz, calcite and barite, are very apt to be present. It will be found in almost every state, especially in fissures and veins, and less frequently in cavities in limestones.
Usually occurs massive, but may be found in crystals; hardness 4; specific gravity 5.6; color deep red; streak orange; luster subadamantine; translucent on thin edges.
When in crystals zincite forms in hexagonal prisms with hexagonal pyramids on the ends. This is rather rare, most of the zincite being found in massive form. The cleavage is parallel to the prism faces and perfect. The deep red color and orange streak are wholly characteristic.
This mineral is so common at Franklin Furnace, N. J., as to be an important ore, but it is very seldom found elsewhere. This district, asmentioned before, is a peculiar one for zinc minerals. The zinc beds are in a metamorphosed limestone, and into this are intruded numerous dikes of granite. Probably the zinc was originally present in the bed of limestone as smithsonite, calamine and other secondary minerals of zinc. When intruded by the hot granite the smithsonite (carbonate) may well have been altered to the oxide, zincite; while the calamine (hydrous silicate) became the simple silicate, willemite.
Occurs in masses or in crystals; hardness 5.5; specific gravity 4.1; color pale yellow when pure; luster resinous; translucent on thin edges.
Willemite is another of the minerals which are distinctively characteristic of Franklin Furnace, and found elsewhere very rarely. It is so common there as to be one of the principal ores, and mostly occurs in irregular masses, but is also found in crystals. These are hexagonal prisms, with a three-sided (rhombohedral) pyramid on the ends. The color when pure is whitish or greenish-yellow, but with small amounts of impurities it may be flesh-red, grayish-white or yellowish-brown. When in crystals it is easily determined; but when massive it looks like calamine, and can only be distinguished by placing a bit of the mineral in a closed tube and heating it, in which case calamine will give off water vapor, while willemite will not.
This mineral is one of those resulting from metamorphic alteration and is derived fromcalamine, when the latter loses its water of crystallization. It is common at Franklin Furnace, N. J., and also found occasionally elsewhere, as at Salida, Colo., and in Socorro Co., New Mexico.
Occurs as crystalline linings in cavities, or as botryoidal or stalactitic masses; hardness 5; specific gravity 3.4; colorless to white; luster vitreous.
Calamine resembles both smithsonite and willemite when in non-crystalline masses. From the smithsonite it is easily separated by the fact that in nitric acid the smithsonite effervesces and the calamine does not. From willemite it is harder to distinguish, but a piece may be placed in a closed tube and heated. If it is calamine water vapor will be given off, if willemite nothing happens. When calamine occurs in crystals these are orthorhombic and mostly tabular, and the crystals are peculiar in that the two ends are terminated differently.
Both this and smithsonite are secondary minerals and usually occur together when zinc is found in limestones. It is abundant at Franklin Furnace and Sterling Hill, N. J., and also found at Phœnixville, Penn., in Wythe Co., Va., and Granby, Mo.
Usually occurs as incrustations, grains, earthy or compact masses, and as crystals; hardness 5; specific gravity 4.4; color white, yellow, greenish or bluish; streak white; luster vitreous; transparent on thin edges.