Figure 10.

View on the Broad Branch of Rock Creek, Washington, D. C.

The fresh but badly decomposed granitic rock is shown passing upward into material more and more decomposed until it becomes sufficiently pulverulent and soluble to support plant life. The roots showing in the upper part of the picture formerly penetrated the decomposed rock, but have been exposed through quarrying operations. Photograph by George P. Merrill, 1891.

43. Action Of Vegetable Life.—The preliminary condition to vegetation is the formation of soil, but once started, vegetation aids greatly in the decomposition of rocks. Some forms of vegetation, as the lichens, have apparently the faculty of growing on the bare surface of rocks, but the higher order requires at least a little soil. The vegetation acts by shading the surface and thus rendering the action of water more effective, by mechanically separating the rock particles by means of its penetrating roots and by the positive solvent action of the root juices. The rootlets of plants in contact with limestone or marble dissolve large portions of these substances, and while their action on more refractory rocks is slower, it must be of considerable importance. The organic matter introduced into the soil by vegetation also promotes decay still further both directly and by the formation of acids of the humic series. This matter also furnishes a considerable portion of carbon dioxid which is carried by the water to assist in its solvent action.

44. Action of Earth-Worms.—Of animal organisms those most active in the formation of soil are earth-worms. The work of earth-worms has been exhaustively studied by Darwin.[30] The worms not only modify the soil by bringing to the surface portions of the subsoil, but also influence its physical state by making it more porous and pulverulent. According to Darwin the intestinal content of worms has an acid reaction, and this has an effect on those portions of the soil passing through their alimentary canal. The acids, which are formed in the upper part of the digestive canal are neutralized by the carbonate of lime secreted by the calciferous glands of the worms thus neutralizing the free acid and changing the reaction to alkaline in the lower part of the canal. There is a fair presumption that the acids of the worm are of a humic nature.

The worms further modify the composition of the soil by drawing leaves and other organic matter into their holes, and leaving therein a portion of such matter which is gradually converted into humus. Stockbridge[31] gives a striking illustration of this process due to an experiment by von Hensen. Darwin estimates that about eleven tons of organic matter per acre are annually added to the soil in regions where worms abound. A considerable portion of the ammonia in the soil at any given time may also be due to the action of worms, as much as 0.18 per cent of this substance having been found in their excrement. It is probable that nearly the whole of the vegetable matter in the soil passes sooner or later through the alimentary canals of these ceaseless soil builders, and is converted into the form of humus.

45. Action of Bacteria.—The intimate relations which have been found to subsist between certain minute organisms and the chemical reactions which take place in the soil is a sufficient excuse for noting the effect of other similar organisms in the formation of soils.

In addition to the usual forces active in decomposing rocks Müntz[32] has described the effects of a nitrifying bacillus contributing to the same purpose.

According to him the bare rock usually furnishes a purely mineral environment where organisms cannot be developed unless they are able to draw their nourishment directly from the air. Some nitrifying organisms belong to this class. It has been shown that these bodies can be developed by absorbing from the ambient atmosphere carbonate of ammonia and vapors of alcohol, the presence of which has been determined in the air. According to the observations of Winogradsky, they assimilate even the carbon of the carbon dioxid just as vegetables do which contain chlorophyl. Thus even in the denuded rocks of high mountains the conditions for the development of all these inferior organisms exist. In examining the particles produced by attrition, it is easily established that they are uniformly covered by a layer of organic matter evidently formed by microscopic vegetations. Thus we see, in the very first products of attrition, appearing upon the rocky particles the characteristic element of vegetable soil, viz., humus, the proportion of which increases rapidly with the products of disaggregation collected at the foot of declivities until finally they become covered with chlorophyliferous plants.

In a similar manner the presence of nitrifying organisms has been noted upon rocky particles received in sterilized tubes, and cultivated in an appropriate environment where they soon produce nitrification. The naked rocks of the Alps, the Pyrenees, the Auvergnes and the Vosges, comprise mineralogical types of the most varied nature, viz., granite, porphyry, gneiss, micaschist volcanic rocks and limestones and all these have shown themselves to be covered with the nitrifying ferment. It is known that below a certain temperature these organisms are not active; their action upon the rock is, therefore, limited to the summer period. During the cold season their life is suspended but they do not perish, inasmuch as they have been found living and ready to resume all their activity after an indefinite sleep on the ice of the glaciers where the temperature is never elevated above zero.

The nitrifying ferment is exercised on a much larger scale in the normal conditions of the lower levels where the rock is covered with earth. This activity is not limited to the mass of rock but is continued upon the fragments of the most diverse size scattered through the soil and it gradually reduces them to a state of fine particles. It is therefore a phenomenon of the widest extension.

The action of these micro-organisms according to Müntz is not confined to the surface but extends to the most interior particles of the rocky mass. Where, however, there is nothing of a nitrogenous nature, to nitrify such an organism must live in a state of suspended animation.

When the extreme minuteness of these phenomena is considered there may be a tendency to despise their importance, but their continuity and their generality in the opinion of Müntz place them among the geologic causes to which the crust of the earth owes a part of its actual physiognomy and which particularly have contributed to the formation of the deposits of the comminuted elements constituting arable soil.

The general action of nitrifying organisms in the soil, the nature of these bodies, and the method of isolating and identifying them will be fully discussed in another part of this work.

46. Action of the Air.—The air itself takes an active part in rock decay. Wherever rocks are exposed to decay, there air is found or, at least, the active principle of air, viz., oxygen. The air not only penetrates to a great depth in the earth, but is also carried to much greater depths by water which always holds a greater or less quantity of air in solution. The oxygen of the air is thus brought into intimate contact with the disintegrating materials and in a condition to assist wherever possible in the decomposing processes.

The oxygen acts vigorously on the lower oxids of iron, converting them into peroxids, and thus tends to produce decay.

There are other constituents of rocks which oxygen affects injuriously and thus helps to their final breaking up. It is true that, as a rule, the constituents of rocks are already oxidized to nearly as high a degree as possible, and on these constituents of course the air would have no effect. But on others, especially when helped by water with the other substances it carries in solution, the air may greatly help in the work of destruction.

In a general view, the action of the air in soil formation may be regarded as of secondary importance, and to depend chiefly on the oxidation of the lower to the higher basic forms. These processes, while they seem of little value, have, nevertheless, been of considerable importance in the production of that residue of rock disintegration which constitutes the soil.

47. Classification of Soils According to Deposition.—In regard to their deposition soils are divided into five classes:

1. Those which are formed from the decomposition of crystalline or sedimentary rocks or of unconsolidated sedimentary material in situ.

2. Those which have been moved by water from the place of their original formation and deposited by subsidence (bottom lands, alluvial soils, lacustrine deposits, etc.).

3. Those which have been deposited as débris from moving masses of ice (glacial drift).

4. Soils formed from volcanic ashes or from materials moved by the wind and deposited in low places or in hills or ridges.

5. Those formed chiefly from the decay of vegetable matter, (tule, peat, muck).

48. Qualities of Soils.—In respect of quality, soils have been arbitrarily divided into many kinds. Some of the more important of these divisions are as follows:

1. Sand. Soils consisting almost exclusively of sand.

2. Sandy Loams. Soils containing some humus and clay but an excess of sand.

3. Loams. Soils inclining neither to sand nor clay and containing some considerable portions of vegetable mold, being very pulverulent and easily broken up into loose and porous masses.

4. Clays. Stiff soils in which the silicate of alumina and other fine mineral particles are present in large quantity.

5. Marls. Deposits containing an unusual proportion of carbonate of lime, with often some potash or phosphoric acid resulting from the remains of sea-animals and plants.

6. Alkaline. Soils containing carbonate and sulfate of soda, or an excess of these alkaline and other soluble mineral substances.

7. Adobe. A fine grained porous earth of peculiar properties hereinafter described.

8. Vegetable. Soils containing much vegetable débris in an advanced state of decomposition. When such matter predominates or exists in large proportion in a soil the term tule, peat or muck is applied to it.

With the exception of numbers six, seven and eight these types of soil are so well-known as to require no further description for analytical purposes. The alkaline, adobe and vegetable soils on the contrary demand further study.

49. Alkaline Soils.—The importance of a more extended notice of this class of soils for analytical purposes is emphasized by their large extent in the United States.

Chiefly through the researches of Hilgard attention has been called to the true character of these soils which are found throughout a large part of the Western United States and which are known by the common name of alkali. The following description of the origin of these soils is compiled chiefly from Hilgard’s papers on this subject. Wherever the rain-fall is scanty, and especially where the rains do not come at any one time with sufficient force to thoroughly saturate the soil and carry down through the subsoil and off through the drainage waters the alkali contained therein, favorable conditions exist for the production of the alkaline soil mentioned above. The peculiar characteristic of this soil is the efflorescence which occurs upon its surface and which is due to the raising of soluble salts in the soil by the water rising through capillary attraction and evaporating from the surface, leaving the salts as an efflorescence.

Soils which contain a large amount of alkali are usually very rich in mineral plant food, and if the excess of soluble salt could be removed, these lands under favorable conditions of moisture would produce large crops.

The formation of the alkali may be briefly described as follows: By the decomposition of the native rocks, certain salts soluble in water are formed. These salts in the present matter are chiefly sodium and potassium sulfates, chlorids and carbonates. The salts of potash together with those of lime are more tenaciously held by the soil than the soluble salts of soda, and the result of this natural affinity of the soil for soluble potash, lime and magnesian salts is seen in the formation at the surface of the earth, by the process of evaporation above described, of a crust of alkaline material which is chiefly composed of the soluble salts of soda. In countries which have a sufficient amount of rain-fall, these soluble salts are carried away either by the surface drainage or by the percolation of water through the soil, and the sodium chlorid is accumulated in this way in the waters of the ocean. But where a sufficient amount of rain-fall does not occur, these soluble salts carried down by each shower only to a certain depth rise again on the evaporation of the water, reinforced by any additional soluble material which may be found in the soil itself. The three most important ingredients of the alkali of the lands referred to are sodium chlorid, sulfate, and carbonate. When the latter salt, namely, sodium carbonate, is present in predominant quantity, it gives rise to what is popularly known as black alkali. This black color is due to the dark colored solution which sodium carbonate makes with the organic matters or humus of the soil. The black alkali is far more injurious to growing vegetation than the white alkali composed chiefly of sodium sulfate and chlorid.

This black alkali has been very successfully treated by Hilgard[33] by the application of gypsum which reacting with the sodium carbonate produces calcium carbonate and sodium sulfate, thus converting the black into the white alkali and adding an ingredient in the shape of lime carbonate to stiff soils which tends to make them more pulverulent and easy of tillage.

This method of treatment, however, as can be easily seen, is only palliative, the whole amount of the alkaline substances being still left in the soil, only in a less injurious form.

The only perfect remedy for alkaline soils, as has been pointed out by Hilgard, is in the introduction of underdrainage in connection with irrigation. The partial irrigation of alkaline soils, affording enough moisture to carry the alkali down to and perhaps partially through the subsoil, can produce only a temporary alleviation of the difficulties produced by the alkali. Subsequent evaporation may thus increase the amount of surface incrustation. For this reason in many cases the practice of irrigation without underdrainage may completely ruin an otherwise fertile soil by slowly increasing the amount of alkali in the soil by the total amount of the alkaline material added in the waters of irrigation.

As Hilgard has pointed out, if a soil can be practically freed from alkali by underdrainage connected with a thorough saturation by irrigation, it may be centuries before the alkali will accumulate in that soil again when ordinary irrigation only is practiced. It may thus become possible to reclaim large extents of alkaline soil little by little by treating them with an excess of irrigation water in connection with thorough underdrainage. The composition of the alkali on the surface of the soil due to the causes above set forth is thoroughly illustrated by the analyses of Hilgard and Weber, which follow:

Table Showing Composition of Alkali Salts in San Joaquin Valley.
FRESNO COUNTY.
Sections 13 and 24 T. 14 S. R. 19 E., 4 miles S. W. from Fresno. Miss Austin’s Ranch, Central Colony. N.W. Cor. N ½ Sec. 20 T. 14 S. R. 21 E. Easton. Emigr’nt Ditch.
Alkali soil, 1888. Alkali Spot, 1889. Surface soil, No. 1. Surface soil, No. 2. Surface soil. Surface soil.
1 inch surface. 18 inches bel. surface. 26 inches bel. surface. 42 inches hardpan.
Soluble salts in 100 parts soil   0.76 0.20 0.18 0.16 3.54 1.90 1.20 2.69    
Potassium sulfate           small moderate        
[D]Potassium nitrate             small        
Potassium carbonate (Saleratus)                      
Sodium sulfate (Glauber’s salt) large small small very slight very slight large large much moderate large  
Sodium carbonate (Sal-soda) very slight large small large large small chiefly small small   chiefly
Sodium chlorid (Common salt) chiefly moderate chiefly moderate moderate chiefly large chiefly chiefly large little
[D]Sodium phosphate                      
Calcium sulfate (Gypsum) moderate small very slight very slight very slight small moderate small small much  
Magnesium sulfate (Epsom salt)             small     much  
Organic matter                      

D. Very generally present, but not always in quantities sufficient for determination.

TULARE COUNTY.
Goshen Peopl’s Ditch Near Lake Tulare Visalia Lemoore Tulare Exp’t Station
Surf’ce soil Alkali crust Surf’ce soil Surf’ce soil Alkali crust Alkali crust
Soluble salts in 100 parts soil 1.40   0.83 1.26    
Potassium sulfate           small
[E]Potassium nitrate           small
Potassium carbonate (Saleratus)       18.80    
Sodium sulfate (Glauber’s salt) 44.24 1.22 31.30[F] 13.4 chiefly 32.8
Sodium carbonate (Sal-soda) 32.98 88.09 18.2 45.3   36.16
Sodium chlorid (Common salt) 16.74 1.00   4.4 little 31.16
[E]Sodium phosphate 1.97   0.22 10.4    
Calcium sulfate (Gypsum)         little  
Magnesium sulfate (Epsom salt)       8.1 moderate  
Organic matter 1.59 9.21 7.5     5.37
KERN COUNTY.
Alkali crusts from the Smyrna artesian belt. Townships 25 and 26 R. 23 E. W. S. W. from Delano, S. P. R. R. Summer. Kern Island
No. 1 No. 2 No. 3 No. 4 No. 5 No. 6 No. 7 No. 8 Alkali crust Alkali crust
Soluble salts in 100 parts soil                    
Potassium sulfate                   4.72
[E]Potassium nitrate                    
Potassium carbonate (Saleratus)                    
Sodium sulfate (Glauber’s salt) small moderate moderate moderate large small small small 19.20 70.61
Sodium carbonate (Sal-soda)                   14.82
Sodium chlorid (Common salt) large moderate large large small large small large 37.14 4.13
[E]Sodium phosphate                    
Calcium sulfate (Gypsum) small small small small small small small small 0.96 0.08
Magnesium sulfate (Epsom salt) small small small small small small small small 18.31  
Organic matter                 20.87  

F. Common and Glauber’s salts.

50. Adobe Soils.—In many parts of the arid regions of this country which can be recovered for agricultural purposes by irrigation the soil has peculiar characteristics.

The name adobe as commonly used applies to both the sundried bricks of the arid regions of the West and Southwest, and to the materials of which they are composed. The material is described by Russell[34] as a fine grained porous earth, varying in color through many shades of gray and yellow, which crumbles between the fingers, but separates most readily in a vertical direction. The coherency of the material is so great that vertical scarps will stand for many years without forming a noticeable talus slope.

Distribution.—The area over which adobe forms a large part of the surface has not been accurately mapped, but enough is known to indicate that it is essentially co-extensive with the more arid portions of this country. In a very general way it may be considered as being limited to the region in which the mean annual rain-fall is less than twenty inches. It forms the surface over large portions of Colorado, New Mexico, Western Texas, Arizona, Southern California, Nevada, Utah, Southern Oregon, Southern Idaho, and Wyoming. Adobe occurs also in Mexico and may there reach a greater development than in the United States, but observations concerning it south of the Rio Grande are wanting.

In the United States it occurs from near the sea-level in Arizona, and even below the sea-level in Southern California, up to an elevation of at least six or eight thousand feet, along the eastern border of the Rocky Mountains, and in the elevated valleys of New Mexico, Colorado, and Wyoming. It occupies depressions of all sizes up to valleys having an area of hundreds of square miles. Although occurring throughout the arid region, it can be studied to best advantage in the drainless and lakeless basins in Nevada, Utah, and Arizona.

Composition.—When examined under the microscope, the adobe is seen to be composed of irregular, unassorted flakes and grains, principally quartz, but fragments of other minerals are also present. An exhaustive microscopic study has not been made, but the samples examined from widely-separated localities were very similar. The principal characteristics observed were the extreme angularity of the particles composing the deposit and the undecomposed condition of the various minerals entering into its composition. It is to be inferred from this that the material was not exposed even to a very moderate degree of friction, and had not undergone subaerial decay before being deposited. Adobe collected, at typical localities is so fine in texture that no grit can be felt when it is rubbed between the fingers; in other instances it contains angular rock fragments of appreciable size.

The composition of the material is illustrated by the following analyses:

Analyses of Adobe.
         
By L. G. Eakins.
         
Constituents. No. 1.
Sante Fe, New Mexico.
No. 2.
Fort Wingate, New Mexico.
No. 3.
Humboldt, Nevada.
No. 4.
Salt Lake City, Utah.
SiO₂ 66.69 26.67 44.64 19.24
Al₂O₃ 14.16 0.91 13.19 3.26
Fe₂O₃ 4.38 0.64 5.12 1.09
MnO 0.09 trace 0.13 trace
CaO 2.49 36.40 13.91 38.94
MgO 1.28 0.51 2.96 2.75
K₂O 1.21 trace 1.71 trace
Na₂O 0.67 trace 0.59 trace
CO₂ 0.77 25.84 8.55 29.57
P₂O₅ 0.29 0.75 0.94 0.23
SO₃ 0.41 0.82 0.64 0.53
Cl 0.34 0.07 0.14 0.11
H₂O 4.94 2.26 3.84 1.67
Organic matter 2.00 5.10 3.43 2.96
 



  99.72 99.97 99.84 100.35

51. Vegetable Soils.—The heavy soils whose origin has been described are essentially of a mineral nature. The quantity of organic matter in such soils may vary from a mere trace to a few per cent, but they never lose their mineral predominance. When a soil on the other hand is composed almost exclusively of vegetable mold it belongs to quite another type. Such soils are called tule, peat or muck. In this country there are thousands of acres of peat or muck soils; the largest contiguous deposits being found in Southern Florida. The origin of these soils is easily understood. Whenever rank vegetation grows in such a location as to secure for the organic matter formed a slow decay there is a tendency to the accumulation of vegetable mold in shallow water or on marshy ground and where conditions are favorable to such accumulations. In Florida the muck soils have been accumulated about the margins of lakes. During the rainy season the marshes bordering these are partly covered with water, but the vegetation is very luxuriant. The water protects the vegetable matter from being destroyed by fire. It therefore accumulates from year to year and is gradually compacted into quite a uniform mass of vegetable mold.

The composition of the muck is illustrated in the following table which shows the character of the layers at one, two and three feet in depth:[35]

Carbon. Hydrogen. Nitrogen. Volatile matter.
1 foot 57.67 per cent 4.48 per cent 2.24 per cent 90.60 per cent
2 feet 47.07 5.15 1.40 72.00
3 feet 8.52 0.53 0.31 15.00

In this sample, No. 3, the muck was only three feet deep, resting on pure sand. As the bottom of the deposit is approached the admixture of sand becomes greater and the percentage of organic matter less.

No reliable estimate of the time which has been required to form these deposits can be given, but in the Okeechobee region in Florida the deposit of vegetable mold in some places exceeds ten feet in depth.

The purest muck or peat soils contain only small quantities of potash and phosphoric acid, and especially is this true of the Florida mucks which have been formed of vegetable growth containing very little mineral matter.

It is not at all probable that the flora now growing on any particular area of virgin peat contains all the plants that have contributed to its formation. The principal vegetable growths now going to make up the muck soils of Florida are the following:

Common names. Botanical names.
Saw grass Cladium effusum
Yellow pond lily Nymphea flava
Maiden cane grass Panicum Curtisii
Alligator Wampee Pontederia cordata
Sedge Cyperus species
Fern brake Osmunda „
Mallow Malva „
Broom sedge Andropogon „
Arrow weed Sagittaria „

The above are only the plants growing in the greatest profusion and do not include all which are now contributing to increase the store of vegetable débris.

52. Humus.—The active principle of vegetable mold is called humus, a term used to designate in general the products of the decomposition of vegetable matter as they are found in soils. In peat and muck are found a mixture of humus with undecomposed or partially decomposed vegetation.

According to Kostytchoff[36] vegetable matter decays under the influence of molds and bacteria. Molds alone produce the dark colored matters which give soils rich in vegetable matter, their color. One chief characteristic of humus is its richness in nitrogen. Black Russian soil contains from 4 to 6.65 per cent of nitrogen. This soil is estimated to contain sixty million organisms per gram and much of the nitrogen which it holds must be in the form of proteids. The first development in decaying vegetable matter is of bacteria and there is a tendency of the decaying matter to become acid. This causes a decay of the bacteria and the ammonia produced by this neutralizes the acid. The various kinds of mold grow when the reaction becomes neutral. Afterwards the bacteria and the molds develop together. This statement of Kostytchoff is not a very satisfactory explanation of even our limited knowledge of the decomposition of organic matters in the soil. Ammonia and ammonia salts are formed not by the decay of some forms of bacteria but by the activities of other forms. Warington found that in nitrification there were three distinct forms of bacteria concerned in the final products of ammonia, nitrites, and nitrates. Humus always contains easily decomposable matter and consequently the rate of decay at any observed periods is nearly the same. In humus which is produced above the water-level Kostytchoff states that all trace of the vegetable structure is destroyed by the leaves being gnawed and passed through the bodies of caterpillars and wire-worms. Under the water-level the vegetable structure is preserved and peat results. The decay of humus is most rapid in drained and open soils. For this reason the presence of clay in a soil promotes the accumulation of humus. Inferior organisms are the means of diffusing organic matter through the soil. The mycelia of fungi grow on a dead root for instance, ramify laterally and thus carry organic matter outward and succeeding organisms extend this action and the soil becomes darkened in proportion. Humic acid in black soil is almost exclusively in combination with lime.

A more common view of the difference between the formation of humus above and below the water-level is that above the water-level there is a very free access of air and even the harder parts of the leaf skeleton can be oxidized through the agency of bacteria, while under the water-level there is a very limited supply of air and this oxidation cannot proceed as rapidly. The harder parts of the leaf skeleton are preserved, and from the freer access of air humus is oxidized more readily in drained and open soils, and accumulates in clay soils where there is less circulation of air.

The real composition of humus is a matter which has never been definitely determined. Composed of many different but closely related substances it has been difficult to isolate and determine them.

Stockbridge[37] gives the following composition of the bodies which form the larger part of humus:

Ulmin and Ulmic Acid.
Carbon 67.1 per cent Corresponding to C₄₀H₂₈O₁₂ + H₂O.
Hydrogen 4.2
Oxygen 8.7
       
Humin and Humic Acid.
       
Carbon 64.4 per cent Corresponding to C₂₁H₂₄_O₁₂ + 3H₂O
Hydrogen 4.3
Oxygen 31.3
       
Crenic Acid.
       
Carbon 44.0 per cent Corresponding to C₁₂H₁₂O₈?
Hydrogen 5.5
Nitrogen 3.9
Oxygen 46.6
       
Apocrenic Acid.
       
Carbon 34.4 per cent Corresponding to C₂₄H₂₄O₁₂?
Hydrogen 3.5
Nitrogen 3.0
Oxygen 39.1

He further states that there are, aside from these humus compounds, others still less known and the action of which is not yet understood; among them xylic acid, C₂₄H₃₀O₁₇, saccharic acid, C₁₄H₁₈O₁₁, glucinic acid, C₁₂H₂₂O₁₂, besides a brown humus acid containing carbon, 65.8 per cent, and hydrogen, 6.25 per cent, and a black humus acid yielding carbon, 71.5 per cent, and hydrogen, 5.8 per cent.

According to Mulder humic acid has the following composition, C₆₀H₅₄O₂₇, while Thenard[38] ascribes to it the formula, C₂₄H₁₀O₁₀.

At the present time we can only regard the various forms of humus bodies as mixtures of many substances mostly of an acid nature and resulting from a gradual decomposition of organic matter under conditions which partially exclude free access of oxygen.

For analytical purposes it is only necessary to separate these bodies by the best approved processes. A further knowledge of their composition can then be derived by determining the percentages of carbon dioxid and water which they yield on combustion.

53. Soil and Subsoil.—Many subdivisions have been made of the above varieties of soil, but they have little value for analytical purposes. For convenience in description for agricultural purposes, the soil, however, is further divided into soil and subsoil. In this sense the soil comprises that portion of the surface of the ground, usually from four to nine inches deep, containing most of the organic remains of plants and animals and in which air circulates more or less freely for the proper humification of the organic matter, which usually gives a darker color to the soil than to the subsoil. The subsoil proper lies below this, and has usually more characteristic properties, especially in respect of color and texture, as it has been less influenced by artificial conditions of cultivation and the remains of vegetation.

The subsoil extends to an indefinite depth and is limited usually by deposits of undecomposed or partly decomposed rock matter, or by layers of clay, sand or gravel.

Inasmuch, however, as the influence of the subsoil on growing crops is of little importance below the depth of eighteen inches the analysis of samples from a greater depth has more of a geologic than agricultural value.

Hilgard regards as subsoil whatever lies beneath the line of change, or below the minimum depth of six inches. But should the change of color occur at a greater depth than twelve inches, the soil specimen should nevertheless be taken to the depth of twelve inches only, which is the limit of ordinary tillage; then another specimen from that depth down to the line of change, and then the subsoil specimens beneath that line. The depth to which the last should be taken will depend upon circumstances. It is always desirable to know what constitutes the foundation of a soil to the depth of three feet at least, since the question of drainage, resistance to drought, etc., will depend essentially upon the nature of the substratum. But in ordinary cases ten or twelve inches of subsoil will be sufficient. The sample should be taken in other respects precisely like that of the surface soil, while that of the material underlying this subsoil may be taken with less exactness, perhaps at some ditch or other easily accessible point, and should not be broken up like the other specimens.

In the method of soil sampling adopted by the Royal Agricultural College of England, the soil is regarded as that portion of the surface of the ground which is reached by ordinary tillage operations, generally being from six to nine inches deep; the subsoil is that portion which is ordinarily not touched in plowing.

AUTHORITIES CITED IN PART FIRST.