4. The prompt conversion of vegetable matter into black, neutral humus, and (as shown in the case of the soils of the arid region) the concentration of the nitrogen in the same; while accelerating the oxidation of the carbon and hydrogen, as shown by S. W. Johnson and others.
6. It counteracts the deleterious influence of an excess of magnesia in the soil, as first shown by Loew,[127] and verified by his pupils in Japan.
7. In alkali soils, according to Cameron and May, it counteracts the injurious action of the soluble salts upon the growth of plants, not only in the form of carbonate, but also in those of sulfate and chlorid.[128]
8. As a matter of experience, both in the case of grapes and orchard as well as wild fruits, an adequate but not excessive supply of lime in the soil will produce sweeter fruit than when lime is in small supply.
9. An excess of carbonate of lime in soils (from eight to twenty per cent and more), constituting “marliness,” tends to seriously disturb the nutrition and general functions of many plants (calcifuge), and to produce a suppression or diminution of the formation of chlorophyll and starch; as in the case of grape vines, citrus fruits and others, which nevertheless flourish best in lands moderately calcareous.
Among the points thus enumerated the third and fourth require some comment. Without pretending to define exactly how lime acts in rendering other ingredients more available to plant assimilation, attention may be called to the fact that lime carbonate may be considered as acting similarly to, albeit more mildly than, caustic lime, in the displacement of other bases from their compounds. It doubtless acts thus in liberating potash from its zeolitic compounds. As to phosphoric acid, the connection of the effect of lime carbonate with the remarkable availability of that substance when present in the form of tetra-basic salt, in the case of phosphate slag, is at least possible.
As to the action of lime carbonate in forming humus,[129] no one who has observed the characteristic dark black tint of our calcareous “prairie soils” can question the fact; which moreover is perfectly explicable upon the analogy already alluded to, with caustic lime, which, together with caustic alkalies (potash and soda), is known to act powerfully in the conversion of vegetable matter into humus. That instead of liberating the nitrogen in the form of ammonia, as do the caustic hydrates, the milder carbonate should only cause the formation of humic amides, is quite intelligible. That such is really the case, has been conclusively proved by the investigations of the writer made conjointly with M. E. Jaffa (Rep. Sta. Cal. Agr. Expt. 1892-4); the general result being that while in the humid region the average nitrogen-content of soil-humus is less than 5%, in the upland soils of the arid region (where all soils are calcareous) that percentage rises as high as 22.0%, with a general average of between 15 and 16%. That such highly nitrogenous material can be more readily attacked by the nitrifying bacteria than when a large excess of other oxidable matter is present, is at least a legitimate presumption, especially in view of the very active nitrification known to take place in the arid regions everywhere. So long as a large excess of carbohydrates is present, the oxidation of these will naturally take precedence over that of the relatively inert nitrogen. The accumulation of the latter in the humus-substance of the arid region, where oxidation of the organic matter of the soil is very active, points strongly to this view of the case.
Magnesia.—While the differences in respect to the proportions of lime are the most prominent and decided, yet the related substance, magnesia, shows also a very marked and constant difference as between the soils of the humid and arid regions. It will be observed that the general average for magnesia in the soils of the Atlantic Slope is about double that of lime; Florida and Rhode Island being the only states in which the average is lower for magnesia than for lime. In the arid region, on the contrary, magnesia on the general average is nearly the same as lime; in the average by states, somewhat less; thus bringing the ratio for the two regions for magnesia up to one to six or seven. This also is so decisive a showing that no accident could bring it about. We must conclude that climatic influences have dealt with magnesia similarly as with lime; which from the standpoint of the chemist is just what might be expected, since magnesia carbonate behaves very much like that of lime toward carbonated waters.
That magnesia is a very important plant-food ingredient is apparent from its invariable and rather abundant presence in the seeds of plants, where it takes precedence of lime. Its functions in plant nutrition have been specially investigated by O. Loew,[130] particularly with respect to its relations to lime. As already stated in connection with the soil-forming properties of magnesian minerals ([see chapter 2]), soils containing large proportions of magnesia generally are found to be unthrifty, the lands so constituted being frequently designated as “barrens.” Loew finds that certain proportions of lime to magnesia must be preserved if production is to be satisfactory, the proportion varying with different plants, some of which (e. g. oats) will do well when the proportion of lime to magnesia is as 1:1, while others require, that that ratio should be as 2 or 3 is to 1, to secure the best results. In general it is best that lime should exceed magnesia in amount.
Loew explains the injurious action of magnesium salts thus: The calcium nucleo-proteids of the organic structures are transformed in presence of soluble salts of magnesium into magnesium compounds, while the calcium of the former enters into combination with the acid of the magnesium salt. By this transformation the capacity for imbibition will change, which must result in a fatal disturbance of functions. The presence of soluble lime salts will prevent that interchange. Thus certain algæ perished in a solution containing 1 per 1000 of magnesium nitrate, but remained alive when .3 per 1000 of calcium nitrate was added.