I.—Phænogamous or Flowering Plants (part 5)

Description—The leaves are dark green, ¾ to 1 inch in length by ²/₈ to ⅜ of an inch in breadth, obovate, rounded at the end, gradually narrowed into a short petiole. They are entire, with the margin a little reflexed, and in the young state slightly pubescent, otherwise the whole leaf is smooth, glabrous, and coriaceous; the upper surface shining, deeply impressed with a network of veins; the under minutely reticulated with dark veins. The leaves have a very astringent taste, and when powdered a tea-like smell.

Chemical Composition—Kawalier (1852) has shown that a decoction of bearberry treated with basic acetate of lead yields a gallate of that metal, thus proving that gallic acid exists ready-formed in the leaves. When the filtrate, freed from lead by sulphuretted hydrogen, is properly concentrated, it deposits acicular crystals of Arbutin, a bitter neutral substance, easily soluble in hot water, less so in cold, dissolving in alcohol, but sparingly in ether.

By contact for some days with emuslin, or by boiling with dilute sulphuric acid, arbutin is resolved, according to Hlasiwetz and Habermann (1875), as follows:—

C₂₅H₃₄O₁₄ + 2 OH₂ = C₆H₁₂O₆ · C₆H₄(OH)₂ · C₆H₄(OH·OCH₃)

Arbutin. Glucose. Hydrokinone. Methyl-
hydrokinone.

Yet possibly arbutin is a mixture of the glucoside compounds of both hydrokinone and methyl-hydrokinone.

By heating arbutin with peroxide of manganese and dilute sulphuric acid, on the other hand, Kinone, C₆H₄O₂, and formic acid are produced. If a concentrated decoction of the leaves is allowed to stand for some months, a decomposition of the arbutin takes place, and a certain quantity of hydrokinone can be isolated by shaking the liquid with ether.

Arbutin is apparently widely distributed among the plants belonging to the order Ericaceæ. Maisch in 1874 showed it to occur in Arctostaphylos glauca Swindley, Gaultheria procumbens L. (Wintergreen) and several other allied American plants. Kennedy (1875) isolated arbutin from Kalmia latifolia L. (Spoonwood), where it occurs in smaller quantity than in bearberry leaves.

Kinic acid (see p. 363) is probably absent in all these plants containing arbutin.

Uloth (1859) had already noticed pyrocatechin (p. 244) and hydrokinone among the products of the distillation of an aqueous extract of bearberry leaves. Arbutin itself also yields hydrokinone by means of dry distillation. Hydrokinone forms colourless crystals, melting at 169° C.

In the mother-liquor from which the arbutin has crystallized, there remains a small quantity of the very bitter substance called Ericolin, occurring in greater abundance in Calluna, Ledum, Rhododendron, and other Ericaceæ. Ericolin is an amorphous yellowish mass, softening at 100° C. and resolved, when heated with dilute sulphuric acid, into sugar and Ericinol, a colourless, quickly resinifying oil of a peculiar, not disagreeable odour; its composition agrees with the formula C₁₀H₁₆O. The same, or C₂₀H₃₂O₂, is to be assigned to Ursone, which H. Trommsdorff, in 1854, obtained from bearberry leaves by exhausting them with ether (in which however it is but slightly soluble). Ursone is a colourless and tasteless crystallizable substance. It melts at 200° C., and sublimes apparently unchanged. Tonner (1866) met with it in the leaves of an Australian Epacris, a plant of the same order as the bearberry.

Lastly, tannic acid is present in the leaves under notice; their aqueous infusion is nearly colourless, but assumes a violet hue on addition of ferrous sulphate. After a short time a reddish precipitate is produced, which quickly turns blue. By using ferric chloride, a bluish black precipitate immediately separates.

Adulteration—The leaves of Vaccinium Vitis-idæa L., called Red Whortleberry or Cowberry, have been confounded with those of bearberry, which in form they much resemble. But they are easily distinguished by being somewhat crenate towards the apex, dotted and reticulate on the under surface and more revolate at the margin.

Uses—An astringent tonic used chiefly in affections of the bladder.

Ebenaceæ.

Fructus Diospyri.

Indian Persimmon.

Botanical Origin—Diospyros Embryopteris Pers. (Embryopteris glutinifera Roxb.), a middle-sized or large evergreen tree, native of the western coast of India, Ceylon, Bengal, Burma, Siam, and also Java.

History—The tree, which is mentioned in the earliest epic poems of the Sanskrit literature under the name of tinduka, was also known about the year 1680 to Rheede, and was figured in his Hortus Malabaricus. The circumstance that the unripe fruit abounds in an astringent viscid juice which is used by the natives of India for daubing the bottoms of boats, was communicated by Sir William Jones to Roxburgh in 1791. The introduction of the fruit into medicine, which is due to O’Shaughnessy, has been followed by its admission to the Pharmacopœia of India, 1868.

Description—The fruit is usually solitary, subsessile or pedunculate, globular or ovoid, 1½ to 2 inches long, and as much as 1½ inch in diameter, surrounded at the base by a large and deeply 4-lobed calyx. It is of a yellowish colour, covered with a rusty tomentum; internally it is pulpy, 6-to 10-celled, with thin flat solitary seeds. The fruit is used only in the unripe and fresh state; the pulp is then excessively astringent. At maturity, in the month of April near Bombay, the fruit becomes eatable, but is very little appreciated.

Chemical Composition—No analysis has been made of this fruit, but there can be no doubt that in common with that of other species of Diospyros, it is, when immature, rich in tannic acid. Charropin (1873), who has examined the fruit of the American D. virginiana L., found it to contain a tannic acid which he considered identical with that of nutgalls, besides an abundance of pectin, glucose, and a yellow colouring matter insoluble in water but dissolving freely in ether.

Uses—The inspissated juice has been recommended as an astringent in diarrhœa and chronic dysentery.

Styraceæ.

Resina Benzoë.

Benzoïnum; Benzoin, Gum Benjamin; F. Benjoin; G. Benzoëharz.

Botanical Origin—Styrax Benzoin Dryander, a tree of moderate height, with stem as thick as a man’s body and beautiful crown of foliage, indigenous to Sumatra and Java, in the first of which islands benzoin is produced.

The tree yielding the superior benzoin of Siam, though commonly referred to this species, has never been examined botanically, and is actually unknown. The French expedition for the exploration of the Mekong and Cochin China (1866-68), reported the drug to be produced in the cassia-yielding forests on the eastern bank of the river in question in about N. lat. 19°. Whether any benzoin is obtained from S. Finlaysoniana Wall, as conjectured by Royle, we know not.

History—There is no evidence that the Greeks and Romans, or even the earlier Arabian physicians, had any acquaintance with benzoin; nor is the drug to be recognized among the commodities which were conveyed to China by the Arab and Persian traders between the 10th and 13th centuries, though the camphor of Sumatra is expressly named.

The first mention of benzoin known to us (disregarding the word kalanusari, which in the St. Petersburg Dictionary is given as the old Sanskrit name of benzoin) occurs in the travels of Ibn Batuta, who having visited Sumatra during his journey through the East, a.d. 1325-49, notes that the island produces Java Frankincense and camphor. The word Java was at that period a designation of Sumatra, or was even used by the Arabs to signify the islands and productions of the Archipelago generally. Hence came the Arabic name Lubán Jáwí, i.e. Java Frankincense, corrupted into Banjawi, Benjui, Benzui, Benzoë and Benzoïn, and into the still more vulgar English Benjamin.

We have no further information about the drug until the latter half of the following century, when we find a record that in 1461 the sultan of Egypt, Melech Elmaydi, sent to Pasquale Malipiero, doge of Venice, a present of 30 rotoli of Benzoi, 20 rotoli of Aloes Wood, two pairs of Carpets, a small flask of balsam (of Mecca), 15 little boxes of Theriaka, 42 loaves of Sugar, 5 boxes of Sugar Candy, a horn of Civet, and 20 pieces of Porcelain. Agostino Barbarigo, another doge of Venice, was presented in a similar manner in 1490 by the sultan of Egypt with 35 rotoli of Aloes Wood, the same quantity of Benzui and 100 loaves of Sugar.

Among the precious spices sent from Egypt in 1476 to Caterina Cornaro, queen of Cyprus, were 10 lb. of Aloes Wood and 15 lb. of Benzui. These notices indicate the high value set upon the drug when first brought to Europe.

The occurrence of benzoin in Siam is noticed in the journal of the voyage of Vasco da Gama, where, in enumerating the kingdoms of India, it is stated that Xarnauz (Siam) yields much benzoin worth 3 cruzados, and aloes worth 25 cruzados per farazola. According to the same record, the price of benzoin (beijoim) in Alexandria was 1 cruzado per arratel, half the value of aloes wood.

The Portuguese traveller Barbosa visited in 1511 Calicut on the Malabar Coast, and found Benzui to be one of the more valuable items of export, one farazola (22 lb. 6 oz.) costing 65 to 70 fanoes; camphor fetched nearly the same price, and mace only 25 to 30 fanoes. From other sources we gather that benzoin was an article of Venetian trade in the beginning of the 16th century.

Garcia de Orta, writing at Goa (1563), was the first to give a lucid and intelligent account of benzoin, detailing the method of collection, and distinguishing the drug of Siam and Martaban from that produced in Java and Sumatra.

It began then to be regularly imported into Europe, being frequently called Asa dulcis. The chemists of that time submitted it, like many other substances, to dry distillation. Benzoic acid occasionally separating from the oily products (“oleum Benzoës”) was noticed already by Nostredame, Rosello, Liebaut, Blaise de Vigenère, and others. It was a common pharmaceutical preparation, under the name of Flores Benzoës, since the 17th century.

In the early part of the 17th century, there was direct commercial intercourse between England and both Siam and Sumatra, an English factory existing at Ayuthia (Siam) until 1623; and benzoin was doubtless one of the commodities imported. The import duties levied upon it in England in 1635 amounted to 10s. per lb.

Production—Benzoin is collected in Northern and Eastern Sumatra, especially in the Batta country, lying southward of the state of Achin. The tree grows in plenty also in the highlands of Palembang in the south and its resin is collected. It is chiefly on the coast regions that considerable plantations are found. Teysmann saw the cultivation in the tracts of the river Batang Leko, the trees being planted about 15 feet apart. The benzoin from the interior is mostly from wild trees, which occur at the foot of the mountains at an elevation of 300 to 1000 feet.

The trees, which are of quick growth, are raised from seeds grown on the [edges of?] rice-fields; they require no particular attention beyond being kept clear of other plants, until about 6 or 7 years old, when they have trunks 6 to 8 inches in diameter, and are capable of yielding the resin. Incisions are then made in their stems, from which there exudes a thick, whitish, resinous juice, which soon hardens by exposure to the air, and is carefully scraped off with a knife.

The trees continue to yield at the rate of about three pounds per annum for 10 or 12 years, after which period they are cut down. The resin which exudes during the first three years is said to be fuller of white tears, and therefore of finer quality, than that which issues subsequently, and is termed by the Malays Head Benzoin. That which flows during the next 7 or 8 years, is browner in colour and less valuable, and is known as Belly Benzoin; while a third sort, called Foot, is obtained by splitting the tree and scraping the wood; this last is mixed with much bark and refuse.

Benzoin is brought for sale to the ports of Sumatra in large cakes called Tampangs, wrapped in matting. These have to be broken, and softened either by the heat of the sun or by that of boiling water, and then packed into square cases which the resin is made to fill.

The only account of the collection of Siam Benzoin is that given by Sir R. H. Schomburgk, for some years British Consul at Bangkok. He represents that the bark is gashed all over, and that the resin which exudes, collects and hardens between it and the wood, the former of which is then stripped off. This account is confirmed by the aspect of some of the Siam benzoin of commerce as well as by that of pieces of bark in our possession; but it is also evident that all the Siam drug is not thus obtained. Schomburgk adds, that the resin is much injured and broken during its conveyance in small baskets on bullocks’ backs to the navigable parts of the Menam, whence it is brought down to Bangkok.

Whether benzoin owes its original fluidity to a volatile oil holding the resin in solution, and its solidification to the volatilization of this oil, or whether the resin itself hardens by oxidation,—what occasions the remarkable diversity of aspect between the opaque and milk-like, and the completely transparent resin, are questions to be investigated by some future observer.

Description—Benzoin (always termed in English commerce Gum Benjamin) is distinguished as of two kinds, Siam and Sumatra. Each sort occurs in various degrees of purity, and under considerable differences of appearance.

1. Siam Benzoin—The most esteemed sort is that which consists entirely of flattened tears or drops, an inch or two long, of an opaque, milk-like, white resin, loosely agglutinated into a mass. More frequently the mass is quite compact, consisting of a certain proportion of white tears of the size of an almond downwards, imbedded in a deep, rich amber-brown, translucent resin. Occasionally the translucent resin preponderates, and the white tears are almost wanting. In some packages, the tears of white resin are very small, and the whole mass has the aspect of a reddish-brown granite. There is always a certain admixture of bits of wood, bark, and other accidental impurities.

The white tears when broken, display a stratified structure with layers of greater or less translucency. By keeping, the white milky resin becomes brown and transparent on the surface.

Siam benzoin is very brittle, the opaque tears showing a slightly waxy, the transparent a glassy fracture. It easily softens in the mouth and may be kneaded with the teeth like mastich. It has a delicate balsamic, vanilla-like, fragrance, but very little taste. When heated it evolves a more powerful fragrance, together with the irritating fumes of benzoic acid; its fusing point is 75° C. The presence of benzoic acid may be shown by the microscopical examination of splinters of the resin under oil of turpentine.

Siam benzoin is imported in cubic blocks, which takes their form from the wooden cases in which they are packed while the resin is still soft.

2. Sumatra Benzoin—Prior to the renewal of direct commercial intercourse with Siam in 1853, this was the sort of benzoin most commonly found in commerce.

It is imported in cubic blocks exactly like the preceding, from which it differs in its generally greyer tint. The mass however, when the drug is of good quality, contains numerous opaque tears, set in a translucent, greyish-brown resin, mixed with bits of wood and bark. When less good, the white tears are wanting, and the proportion of impurities is greater. We have even seen samples consisting almost wholly of bark. In odour, Sumatra benzoin is both weaker and less agreeable than the Siam drug, and generally falls short of it in purity and handsome appearance, and hence commands a much lower price. The greyish-brown portion melts at 95°, the tears at 85° C.

A variety of Sumatra benzoin is distinguished by the London drug-brokers as Penang Benjamin or Storax-smelling Benjamin. We have seen it of very fine quality, full of white tears (some of them two inches long), the intervening resin being greyish. The odour is very agreeable, and perceptibly different from that of Siam benzoin, or the usual Sumatra sort. Whether this drug is produced in Sumatra and by Styrax Benzoin we know not; but it is worthy of note that S. subdenticulata Miq., occurring in Western Sumatra, has the same native name (Kajoe Kĕminjan) as S. Benzoin, and that Miquel remarks of it—“An etiam benzoiferum?”

Chemical Composition—Benzoin consists mainly of amorphous resins perfectly soluble in alcohol and in potash, having slightly acid properties, and differing in their behaviour to solvents. If two parts of the drug are boiled with one part of caustic lime and 20 parts of water, benzoic acid is removed. From the residue the excess of lime is dissolved by hydrochloric acid, and the remaining resins washed and dried. About one-third of them will be found readily soluble in ether, the prevailing portion dissolves in alcohol, and a small amount remains undissolved.

By distilling the resin of benzoin with ten times its weight of zinc dust, Ciamician (1878) chiefly obtained toluol, C₆H₅(CH₃).

Subjected to dry distillation, benzoin affords as chief product Benzoic Acid, C₇H₆O₂, together with empyreumatic products, among which Berthelot has proved the presence (in Siam benzoin) of Styrol (p. 274). The latter has been obtained in 1874 by Theegarten from Sumatra benzoë by distilling it with water. When the resin is fused with potash, it is partly decomposed and then, according to Hlasiwetz and Barth (1866), yields among other products, protocatechuic acid (more than 5 per cent.), C₆H₃(OH)₂COOH, para-oxybenzoic acid, C₆H₄(OH)COOH, and pyrocatechin, C₆H₄(OH)₂.

Benzoic acid exists ready-formed in the drug to the extent of 14 to 18 per cent. Although the acid dissolves in 12 parts of boiling water, the resin in which it is imbedded precludes its complete extraction by this means. It is however easily accomplished by the aid of an alkali, most advantageously by milk of lime, which does not combine with the amorphous resins.

Benzoin is not manifestly acted on by bisulphide of carbon, but if kept in contact with it for a month or two, very large colourless crystals of benzoic acid make their appearance. Brought into a warm room, the crystals quickly dissolve, but are easily reproduced by exposure to cold.

Most pharmacopœias require not the inodorous acid obtained by a wet process, but that afforded by sublimation, which contains a small amount of fragrant empyreumatic products. The resin, when repeatedly subjected to sublimation, affords as much as 14 per cent. of benzoic acid. It has long been known that the opaque white tears of benzoin are less rich in benzoic acid than the transparent brown resin in which they lie. From the latter, S. W. Brown (1833) extracted 13 per cent. of impure acid, but from the former scarcely 8½ per cent. We are by no means sure that such difference is constant.

Bitter almond oil, which by oxidation yields benzoic acid, is wanting in benzoin. Very little volatile oil is in fact to be got; half a pound of the best Penang benzoin yielded us by distillation with water only a few drops of an extremely fragrant oil (styrol?).

Ferric chloride imparts to an alcoholic solution of benzoin a dark brownish green, which is not acquired under the same circumstances by the aqueous decoction of the powdered resin. Benzoin dissolves in cold oil of vitriol, forming a solution of splendid carmine hue, from which water separates crystals of benzoic acid.

Kolbe and Lautemann in 1860 discovered in Siam and Penang benzoin together with benzoic acid, an acid of different constitution, which in 1861 they recognized as Cinnamic Acid, C₉H₉O₂. Aschoff (1861) found in a sample of Sumatra benzoin, cinnamic acid only, of which he got 11 per cent.; and in amygdaloid Siam and Penang benzoin only benzoic acid. In some samples of the latter, one of us (F.) has likewise met with cinnamic acid. On triturating this sort with peroxide of lead and boiling the mixture with water, the odour of bitter almond oil, due to the oxidation of cinnamic acid, is evolved.

The simultaneous occurrence of benzoic and cinnamic acids, or the absence of one or other of them in benzoin, is due to circumstances at present unexplained. Rump is of the opinion that the last named acid exclusively is present in the Penang (or Sumatra) benzoin and that no variety of the drug contains both those acids.

Rump (1878) treated Siam benzoic with caustic lime (see p. 407), precipitated the benzoic acid with hydrochloric acid, and agitated the liquid with ether. The latter on evaporating afforded a mixture of benzoic acid and Vanillin (see article Vanilla).

Commerce—The statistics of Singapore, the great emporium of the commerce of the Indian Archipelago, show the imports of Gum Benjamin in 1871 as 7442 cwt., of which quantity 6185 cwt. had been shipped from Sumatra and 405 cwt. from Siam. In 1877 only 1871 peculs (2227 cwts.) were exported from Singapore. Penang, which is also a mart for this drug was stated in 1871 to have received from Sumatra for trans-shipment, 4959 cwt. of Gum Benjamin.

Padang in Sumatra exported in 1870, 4303 peculs (5122 cwt.); and in 1871, 4064 peculs (4838 cwt.) of benzoin.

The imports of Gum Benjamin into Bombay in the year 1871-72 were no less than 5975 cwt., and the exports 1043 cwt.

Uses—Benzoin appears to be nearly devoid of medicinal properties, and is but little employed. It is chiefly imported for use as incense in the service of the Greek Church.

Oleaceæ.

Manna.

Manna; F. Manne; G. Manna.

Botanical Origin—Fraxinus Ornus L. (Ornus europæa Pers.), the Manna-ash, is a small tree found in Italy, whence it extends northwards as far as the Canton of Tessin in Switzerland and the Southern Tyrol. It also occurs in Hungary (Buda) and the eastern coasts of the Adriatic, in Greece, Turkey (Constantinople), in Asia Minor about Smyrna and at Adalia on the south coast. It grows in the islands of Sicily, Sardinia and Corsica, and is found in Spain at Moxente in Valencia. As an ornamental tree it has been introduced into Central Europe, where it is often seen of greater dimensions, sometimes acquiring a height of about 30 feet. It blossoms in early summer, producing numerous feathery panicles of dull white flowers which give it a pleasing appearance. The foliage exhibits great variation in shape of leaflets, even where the tree is uncultivated; and the fruits also are very diverse in form.

In some districts of Sicily, a little manna is obtained from the Common Ash, F. excelsior L.

History—The name Manna, though originally applied to the aliment miraculously provided for the sustenance of the ancient Israelites during their journey to the Holy Land, has been used to designate other substances of distinct nature and origin. Of these, the best known and most important is the saccharine exudation of Fraxinus Ornus L., which constitutes the Manna of European medicine.

It appears evident that previous to the 15th century, the manna in Europe was imported from the East and was not that of the ash. Raffaele Maffei, called also Volaterranus, a writer who flourished in the second half of the 15th century, states that manna began to be gathered in Calabria in his time, but that it was inferior to the oriental. At this period the manna collected was that which exuded spontaneously from the leaves of the tree, and was termed Manna di foglia or Manna di fronda: that which flowed from the stem bore the name of Manna di corpo and was less esteemed. All such manna was very dear.

About the middle of the 16th century, the plan of making incisions in the trunk and branches was resorted to, and although it was strenuously opposed even by legislative enactment, the more copious supplies which it enabled the collectors to obtain led it to being generally adopted. The Ricettario Fiorentino of the year 1573 states that the manna “fatta con arte,” i.e. obtained by incisions, came from Cosenza in Calabria and differed not little from Syrian “manna mastichina.”

Manna di foglia became in fact utterly unknown, so that Cirillo of Naples, writing in 1770, expresses doubt whether it ever had any existence.

With regard to the history of manna-production in Sicily, there is this curious fact, that near Cefalù there exists an eminence in the Madonia range, called Gebelman or Gibelmanna, which in Arabic signifies manna-mountain. This name is not of modern origin, but is found in a diploma of the year 1082, concerning the foundation of the bishopric of Messina; and it has been held to indicate that manna was there collected during the Saracenic occupation of Sicily, a.d. 827 to 1070. We have not been successful in finding any evidence whether this supposition is well founded. On the other hand, it is remarkable that no writer, so far as we know, mentions manna as a production of Sicily, before Paolo Boccone of Palermo, who, after naming many localities for the drug in continental Italy, states that it is also obtained in Sicily.

Manna was also produced until recently in the Tuscan Maremma, but neither from that locality, nor from the States of the Church, where it was collected in the time of Boccone, is any supply now brought into commerce, though the name of Tolfa, a town near Civita Vecchia, is still used to designate an inferior sort of the drug.

The collection of manna in Calabria, which was imported up to the end of last century, has now almost entirely ceased.

Production—The manna of commerce is collected at the present day exclusively in Sicily. The principal localities producing the drug are the districts around Capaci, Carini, Cinisi, and Favarota, small towns 20 to 25 miles west of Palermo near the shores of the bay of Castellamare; also the townships of Geraci, Castelbuono, and other places in the district of Cefalù, 50 to 70 miles eastward of Palermo.

The manna-ash, in the districts whence the best manna is obtained, does not at the present day form natural woods, but is cultivated in regular plantations called frassinetti. The trees, which attain a height of from 10 to 20 feet, are planted in rows and stand about 7 feet apart, the soil between being at times loosened, kept free from weeds, and enriched by manure. After a tree is 8 years old and when its stem is at least 3 inches in thickness, the gathering of manna may begin; and may continue for 10 or 12 years, when the stem is usually cut down, and a young one brought up from the same root takes its place. The same stump thus has often two or three stems rising from it.

To obtain manna, transverse cuts from 1½ to 2 inches long and 1 inch apart, are made in the bark, just reaching to the wood. One cut is made daily, beginning at the bottom of the tree, the second directly above the first, and so on while dry weather lasts. In the following year, cuts are made in the untouched part of the stem, and in the same way in succeeding seasons. When after some years the tree has been cut all round and is exhausted, it is felled. Pieces of sticks or straws are inserted in the incisions, and become encrusted with the very superior manna, called Manna a cannolo, which however is unknown in commerce as a special sort. The fine manna ordinarily seen appears to have hardened on the stem of the tree. The manna which flows from the lower incisions, and is often collected on tiles or on a cup-shaped piece of the stem of the prickly pear (Opuntia), is less crystalline, and more gummy and glutinous, and is regarded of inferior quality.

The best time for notching the stems is in July and August, when the trees have ceased to push forth more leaves. Dry and warm weather is essential for a good harvest. The manna after removal from the tree, is laid upon shelves in order that it may dry and harden before it is packed. The masses left adhering to the stem after the finer pieces have been gathered, are scraped off and form part of the Small Manna of commerce.

Secretion—We have examined microscopically the bark of stems of Fraxinus Ornus that had been incised for manna at Capaci. It exhibits no peculiarity explaining the formation of manna, or any evidence that the saccharine exudation is due to an alteration of the cell-walls as in the case of tragacanth. The bark is poor in tannic matter; it contains starch, and imparts to water a splendid fluorescence due to the presence of Fraxin.

Description—Various terms have been used by pharmacological writers to designate the different qualities of manna, but in English commerce they are not now employed; and the better kinds of the drug are called simply Flake Manna, while the smaller pieces, usually loosely agglutinated and sold separately, are termed Small Manna or Tolfa Manna.

Owing to the gradual exudation of the juice and the deposition of one layer over another, manna has a stalactitic aspect. The finest pieces are mostly in the form of three-edged sticks, sometimes as much as 6 to 8 inches long and an inch or more wide, grooved on the inner side, which is generally soiled by contact with the bark; of a porous, crystalline, friable structure and of a pale brownish yellow tint, becoming nearly pure white in those parts which have been most distant from the bark of the tree. The pieces which are of deeper colour, and of an unctuous or gummy appearance, are less esteemed. Good manna is crisp and brittle, and melts in the mouth with an agreeable, honey-like sweetness, not entirely devoid of traces of bitterness and acridity. Its odour may be compared to that of honey or moist sugar.

Manna of the best quality dissolves at ordinary temperatures in about six parts of water, forming a clear, neutral liquid. It contains besides mannite, a small proportion of sugar and gum.

The manna which exudes from the older stems and from the lower parts of even young trees, contains more or less considerable quantities of gum and fermentable sugar, as well as extraneous impurities. The less favourable weather of the later summer and autumn promotes an alteration in the composition of the juice, and impairs its property of concreting into a crystalline mass.

Chemical Composition—The predominant constituent of manna, at least of the better sorts, is Manna-sugar or Mannite, C₆H₈(OH)₆ which likewise occurs, though in much smaller quantity, in many other plants besides Fraxinus. Artificially, it is produced by treating glucose, C₆H₁₂O₆, with sodium amalgam, and indirectly in the fermentation of glucose or of cane-sugar. It is isomeric with dulcite or melampyrin; crystallizes in shining prisms or tables, belonging to the rhombic system; melts at 166° C., and in very small quantity may by careful heating be sublimed and decomposed. It dissolves in 6·5 parts of water at 16° C., less freely in aqueous alcohol, very sparingly in absolute alcohol, and not in ether. The solution has an extremely weak rotatory power, and is not altered by boiling with dilute acids or alkalis, or with alkaline cupric tartrate.

Berthelot has shown that mannite is susceptible of fermentation, though not so easily as sugars belonging to the group of carbo-hydrates. The quantity of mannite in the best manna varies from 70 to 80 per cent.

When a solution of manna is mixed with alkaline cupric tartrate, rapid reduction to cuprous hydrate takes place even in the cold. This effect is due to the presence of a sugar which, according to Backhaus (1860), consists of ordinary dextro-glucose. It may amount to as much as 16 per cent., and is found in the best flake manna, but most abundantly in the unctuous varieties. Buignet has pointed out that the rotatory power of this sugar being inconsiderable, it probably consists of a mixture of Cane-sugar and Levulose. He found however that an aqueous solution of manna deviates powerfully to the right, a fact which he considers due to the presence of a large proportion of Dextrin. The best kinds of manna, according to Buignet, contain about 20 per cent. of dextrin; the inferior much more.

In our experiments we have not succeeded in isolating either dextrin or cane-sugar. There is present, even in the finest manna, a small amount of a dextrogyre mucilage, which is precipitated by neutral acetate of lead, and yields mucic acid when boiled with concentrated nitric acid.

Ether extracts from an aqueous solution of manna a very small quantity of red-brown resin, having an offensive odour and sub-acrid taste; together with traces of an acid which reduces silver salts and appears to be easily resinified. The quantity of water in the inferior kinds of manna often amounts to 10 or 15 per cent. The finest manna affords about 3·6 per cent. of ash.

The greenish colour of certain pieces of manna was formerly attributed to the presence of copper, till Gmelin, on account of the fluorescence of the solution, ascribed it to Æsculin. It is in reality produced by a body much resembling æsculin, namely Fraxin, C₁₆H₁₈O₁₀, occurring in the bark of the manna-ash and of the common ash, and together with æsculin, in that of the horse-chestnut. Fraxin crystallizes in colourless prisms, easily soluble in hot water and in alcohol, and having a faintly astringent and bitter taste. By dilute acids, it is resolved into Fraxetin, C₁₀H₈O₃, and Glucose, C₆H₁₂O₆. The presence of fraxin in manna, especially in the inferior sorts, is made apparent by the faint fluorescence of the alcoholic manna solution. The smallest fragment of the bark of the ash or the manna-ash immersed in water displays the same fluorescence.

Commerce—The exports of manna from Sicily (chiefly from Palermo) have been as follows:—

1869 1870 187

2546 cwt., 1564 cwt., 3038 cwt.,

val. £15,972. val. £10,220. val. £19,528.

About half the quantity is sent to France. Italian commercial statistics represent the export of manna in 1870 thus:—in canelli 58,691 kilo. (1155 cwt.), in sorte 186,664 kilo. (3676 cwt.). The United Kingdom imported in the year 1870, 230 cwt. of manna, valued at £4447.

In 1877 the exports of “canelli” from Messina were 4273 kilogrammes, and of the drug “in sorte” 52,874 kilogr.; total value, 127,145 lire.

Adulteration—It can hardly be said that manna is subject to adulteration, though attempts to introduce a spurious manna made of glucose have been recorded. But considerable skill and ingenuity have been expended in converting the inferior sorts of manna into what has the aspect of fine natural Flake Manna, the manufacturers admitting however the factitiousness of their product. The artificial Flake Manna has the closest superficial resemblance to very fine pieces of the natural drug, but differs in its more uniform colour, and in being uncontaminated with the slight impurities, from which natural manna is never wholly free. It differs also in that when broken, no crystals of mannite are to be seen in the interstices of the pieces, and it wants the peculiar odour and slightly bitter flavour of natural manna. If one part of it is boiled with four of alcohol (0·838), a viscid honey-like residue will be obtained, whereas natural manna leaves undissolved a hard substance. Histed found it to afford about 40 per cent. of mannite, while fine manna similarly treated yielded 70 per cent.

Uses—A gentle laxative, much less frequently employed in this country than formerly, but still largely consumed in South America. Mannite, which possesses similar properties, is often prescribed in Italy.

Other sorts of Manna.

Various plants besides Fraxinus afford, under certain conditions, saccharine exudations, some of which constituted the Oriental Manna used in Europe in early times. So far as is known, they differ from officinal manna in containing no mannite.

Alhagi Manna; Turanjabín (Arabic); is afforded by Alhagi Camelorum Fisch. (Hedysarum Alhagi Pallas, non L.), a small spiny plant of the order Leguminosæ found in Persia, Afghanistan and Beluchistan. It had already been noticed by Isztachri. Excellent specimens of the manna, kindly obtained for us in the north-west of India by Dr. E. Burton Brown and Mr. T. W. H. Tolbort, show it as a substance in little roundish, hard, dry tears, varying from the size of a mustard seed to that of a hemp seed, of a light brown colour, agreeable saccharine taste, and senna-like smell. The leaflets, spines and pods of the plant, mixed with the grains of this manna, are characteristic and easily recognizable.

Villiers (1877) showed this manna to contain cane-sugar, a dextrogyrate glucose, and melezitose (see further on: Briançon manna, page 416). Ludwig had also found some dextrin and mucilage.

Alhagi Manna is collected near Kandahar and Herat, where it is found on the plants at the time of flowering. It is imported into India from Kabul and Kandahar to the extent of about 25 maunds (2000 lb.) annually; its value is reckoned at 30 rupees per secr, = 30s. per lb.

Gaz-anjabin (Arabic); Tamarisk Manna (in part)—In the months of June and July, the shrubs of tamarisk (Tamarix gallica var. mannifera Ehrenb.) growing in the valleys of the peninsula of Sinai, especially in the Wady es Sheikh, exude from their slender branches, in consequence of the puncture of an insect (Coccus manniparus Ehrenb.) little honey-like drops, which in the coolness of early morning are found in a solid state. This substance is Tamarisk Manna: it is collected by the Arabs, and by them sold to the monks of St. Katharine, who dispose of it to the pilgrims visiting the convent. Tamarisk Manna is also produced (but is perhaps no longer collected?) in Persia, where it is called Gaz-angabín; and probably likewise in the Punjab, from which regions it may have been brought to Europe in ancient times.

A specimen of tamarisk manna brought from Sinai, examined in 1861 by Berthelot, had the appearance of a thick yellowish syrup, contaminated with vegetable remains. It was found to consist of cane-sugar, inverted sugar (lævulose and glucose), dextrin and water, the last constituting one-fifth of the whole.

Although the name Gaz-angabín signifies tamarisk-honey, it is used according to Haussknecht at the present time in Persia, to designate certain round cakes, common in all the bazaars, of which the chief constituent is a manna collected in the mountain districts of Chahar-Mahal and Faraidan, and especially about the town of Khonsar, south-west of Ispahan, from Astragalus florulentus Boiss. et Haussk. and A. adscendens Boiss. et Haussk. The best sorts of this manna, which are termed Gaz Alefi or Gaz Khonsari, are obtained in August by shaking it from the branches, the little drops finally sticking together and forming a dirty, greyish-white, tough mass. The commoner sort got by scraping the stem, is still more impure. The specimen of it brought by Haussknecht yielded to Ludwig dextrin, uncrystallizable sugar and organic acids.

Shir-khist—Ancient writers on materia medica as Garcia d’Orta (1563) mention a sort of manna known by this name. The substance is still found in the bazaars of North-western India, being imported in small quantity from Afghanistan and Turkistan. Haussknecht in his paper on Oriental Manna already quoted, states that it is the exudation of Cotoneaster nummularia Fisch. et Mey. (Rosaceæ), also of Atraphaxis spinosa L. (Polygonaceæ), and that it is brought chiefly from Herat. We have to thank Dr. E. Burton Brown of Lahore, and Mr. Tolbort for specimens of this manna, which, from fragments it contains, is without doubt derived from a Cotoneaster. It is in irregular roundish tears, from about ¼ up to ¾ of an inch in greatest length, of an opaque dull white, slightly clammy, and easily kneaded in the fingers. It has a manna-like smell, a pure sweet taste and crystalline fracture. With water, it forms a syrupy solution with an abundant residue of starch granules.

Shír-khist was found by Ludwig to consist of an exudation analogous to tragacanth, but containing at the same time two kinds of gum, an amorphous levogyre sugar, besides starch and cellulose.

Oak Manna—The occurrence of a saccharine substance on the oak is noticed by both Ovid and Virgil, and it is also mentioned by the Arabian physicians, as Ibn Baytar and Elluchasem Elimithar. The last named, who died a.d. 1052, states that the exudation appears upon the oaks in the region of Diarbekir. At the present day, it is the object of some industry among the wandering tribes of Kurdistan, who, according to Haussknecht, collect it from Quercus Vallonea Kotschy and Q. persica Jaub. et Spach. These trees are visited in the month of August by immense numbers of a small white Coccus, from the puncture of which a saccharine fluid exudes, and solidifies in little grains. The people go out before sunrise, and shake the grains of manna from the branches on to linen cloths, spread out beneath the trees. The exudation is also collected by dipping the small branches on which it is formed, into vessels of hot water, and evaporating the saccharine solution to a syrupy consistence, which in this state is used for sweetening food, or is mixed with flour to form a sort of cake.

A fine specimen of the Oak Manna of Diarbekir was sent to the London International Exhibition of 1862. It constituted a moist soft mass of agglutinated tears, much resembling an inferior sort of ash-manna, and had an agreeable saccharine taste.

A less pure form of this manna occurs as a compact, greyish, saccharine mass, sometimes hard enough to be broken with a hammer. It consists of sugary matter, mixed with abundance of small fragments of green leaves, and has a herby smell and pleasant sweet taste. A sample of it brought from Diarbekir, examined by one of us, yielded 90 per cent. of dextrogyre sugar, which could not be obtained in a crystalline state, though it exists in such condition in the crude drug. Starch and dextrine were entirely wanting.

A specimen furnished to Ludwig by Haussknecht afforded much mucilage, a small amount of starch, about 48 per cent. of dextrogyre grape sugar, with traces of tannic acid and chlorophyll.

Briançon Manna—This is a white saccharine substance which, in the height of summer and in the early part of the day, is found adhering in some abundance to the leaves of the larch (Pinus Larix L.), growing on the mountains about Briançon in Dauphiny. It was formerly collected for use in medicine, but only to a very limited extent, for it was rare in Paris in the time of Geoffroy (1709-1731), and at the present day has quite disappeared from trade, though still gathered by the peasants. A specimen collected for one of us near Briançon in 1854, consists of small, detached, opaque, white tears, many of them oblong and channelled, and encrusting the needle-like leaf of the larch; they have a sweet taste and slight odour. Under the microscope they exhibit indistinct crystals.

Briançon manna has been examined in 1858 by Berthelot, who detected in it a peculiar sugar termed Melezitose, answering to the formula C₁₂H₂₂O₁₁ + OH₂.

Several other saccharine exudations have been observed by travellers and naturalists; we shall simply enumerate the more remarkable, referring the reader for further information to the original notices.

Pirus glabra Boiss. affords in Luristan a substance which, according to Haussknecht, is collected by the inhabitants, and is extremely like Oak Manna. It is stated by the same traveller that Salix fragilis L., and Scrophularia frigida Boiss., likewise yield in Persia saccharine exudations. A kind of manna was anciently collected from the cedar, Pinus Cedrus L. Manna is yielded in Spain by Cistus ladaniferus L. Australian Manna, which is in small rounded, opaque, white, dry masses, is found on the leaves of Eucalyptus viminalis Labill. It contains a kind of sugar called Melitose, has a sweet thistle, is devoid of medicinal properties and is not collected for use.

The substance named Tigala (corrupted into Trehala), from which a peculiar sugar has been obtained, is the coccoon of a beetle, and not properly a saccharine exudation.

The Lerp Manna of Australia is also of animal origin. It consists of water 14, white thread-like portion 33, sugar 53 parts. The threads possess some of the characteristic properties of starch, from which they differ entirely by their form and unalterability even in boiling water. Yet in sealed tubes, they dissolve in 30 parts of water at 135° C. The sugar is dextrogyre; it impregnates the threads as a soft brown amorphous mass. In the purified state it does not crystallize, even after a long time. By means of dilute sulphuric acid, the threads are converted into crystalline grape sugar.

Oleum Olivæ.

Olive Oil; Salad Oil; F. Huile d’Olives; G. Olivenöl; Baumöl; Provencer Oel.

Botanical Origin—Olea europæa L., an evergreen tree, seldom exceeding 40 feet in height, yet attaining extreme old age, abundantly cultivated in the countries bordering the Mediterranean, up to an elevation of about 2000 feet above the sea-level. Olea ferruginea Royle (O. cuspidata Wallich), a tree abundant in Afghanistan, Beluchistan and Western Sind, has been supposed to be a wild form of O. europæa, but is regarded by Brandis as a distinct species. It is not known to have been ever cultivated, yet its fruit, which is of a small size and but sparingly produced, is capable of affording a good oil.

History—In ancient Egypt the olive was known by the term bāk; it can be traced as far as the 17th century before our era.

According to the elaborate investigations of Ritter and of A. De Candolle, the olive tree is a native of Palestine, and perhaps of Asia Minor and Greece. Its original area also extends over north-eastern Africa; Schweinfurth regards it as undoubtedly wild on the mountains of Elbe and Soturba in lat. 22 N. on the western shores of the Red Sea, a locality which he visited in 1868. The olive tree has also been met with as far eastward as the country of the Gallas, where it is much appreciated as affording excellent timber. It is also stated by Theophrastus, that in his time the tree was plentiful in the Cyrenaica, the modern Barca, in northern Africa.

The olive would appear to have been introduced at a very remote period into north-western Africa and Spain. Willkomm (1876) is of the opinion that it was originally a native of the whole Mediterranean region.

At the present day it is largely cultivated in Algeria, Spain, Portugal, Southern France, Italy, the Greek Peninsula and Asia Minor. In the Crimea the tree grows well, but does not afford good fruit. It was carried to Lima in Peru about 1560 and still flourishes there, and in great plenty in the coast valleys further south as far as Santiago in Chili.

Olive oil is mentioned in the Bible so frequently that it must have been an important object with the ancient Hebrews. It held an equally prominent place among the Greeks and Romans, whose writers on agriculture and natural history treat of it in the most circumstantial manner. Olive fruits preserved in brine were used by the Romans as an article of food, and were an object of commerce with Northern Europe as early as the 8th century.

Production—In common with many important cultivated plants, the olive occurs under several varieties differing more or less from the wild form, the finer of which are propagated by grafting. It is also increased by the suckers which old trees throw up from their naked roots, and which are easily made to develope into separate plants. The fruit, an oval drupe, half an inch to an inch or more in length, and of a deep purple, is remarkable for the large amount of fat oil contained in its pulpy portion (sarcocarp). The latter is most rich in oil when ripe, containing then nearly 70 per cent., besides 25 per cent. of water. The unripe fruit, as well as other parts of the plant, abounds in mannite, which disappears in proportion as the oil increases. The ripe olive contains no mannite, it having probably been transformed into fatty oil.

The process for extracting olive oil varies slightly in different countries, but consists essentially in subjecting the crushed pulp of the ripe fruit to moderate pressure. The olives, which are gathered from the trees, or collected from the ground, in November, or during the whole winter and early spring, are crushed under a millstone to a pulpy mass. This is then put into coarse bags, which, piled upon one another, are subjected to moderate pressure in a screw press. The oil thus obtained is conducted into tubs or cisterns containing water, from the surface of which it is skimmed with ladles. This is called Virgin Oil. After it has ceased to flow, the contents of the bags are shovelled out, mixed with boiling water, and submitted to stronger pressure than before, by which a second quality of oil is got. If the fruit is left for a considerable time in heaps it undergoes decomposition, yielding by pressure a very inferior quality of oil called in French Huile fermentée. The worst oil of all, obtained from the residues, has the name of Huile tournante or Huile d’enfer.

It is said that in some districts the millstones are so mounted as to crush the pulp without breaking the olive-stones, and that thus the oil of the pulp is obtained unmixed with that of the kernels. We have made many inquiries in Italy and France as to this method of oil-making, but cannot find that it is anywhere followed.

The fixed oil of the kernels of ripe olives has been extracted and examined by one of us (F.). Though the kernels have a bitterish taste, the oil they yield is quite bland; by exposure to the vapour of hyponitric acid, it concretes like that of the pulp. If the whole of it were extracted in making olive oil, it would only be about as 1 part of oil of the kernel, to 40 parts of oil of the pulp.

Description—Olive Oil is a pale yellow or greenish yellow, somewhat viscid liquid, of a faint agreeable smell and of a bland oleaginous taste, leaving in the throat a slight sense of acridity. Its specific gravity on an average is 0·916 at 17° C. In cold weather, olive oil loses its transparency by the separation of a crystalline fatty body. The deposition takes place at a few degrees above the freezing point of water, and in some oils even at 10° C. (50° F.) If the oil is allowed to congeal perfectly, and is then submitted to strong pressure, about one-third of its weight of solid fat may be separated. After repeated crystallizations, this fat melts at 20 to 28° C. The fluid part or Olein, continues fluid at -4° to -10° C. Olive oil belongs to the class of the less alterable, non-drying oils.

The foregoing description does not apply to the inferior sorts of oil, which congeal more easily, are more or less deep-coloured, have a disagreeable odour and taste, and quickly turn rancid. These inferior oils have their special applications in the arts.

Chemical Composition--The chief constituent of olive oil is Olein or more correctly Triolein, C₃H₅(O·C₁₈H₃₃O)₃, identical so far as at present ascertained with the fluid part of all oils of the non-drying class. The proportion of olein in olive oil, as well as in other oils, is liable to variation, the result partly of natural circumstances and partly of the processes of manufacture. The best oils are rich in olein.

As to the solid part of olive oil, Chevreul believed it to be constituted of Margarin, which he first examined in 1820. But Heintz (1852 and later) showed margarin to be a mixture of palmitin with other compounds of glycerin and fatty acids. Collett in 1854 isolated Palmitic Acid, C₁₆H₃₂O₂, from olive oil; and Heintz and Krug (1857) further proved that Tripalmitin is the chief of the solid constituents of olive oil. They also met with an acid melting at 71°·4 C., which they regarded as Arachic Acid (p. 187). As to stearic acid, Heintz and Krug did not fully succeed in evidencing its presence in olive oil.

Lastly, Benecke discovered in olive oil a small quantity of Cholesterin, C₂₆H₄₄O. It may be removed by means of glacial acetic acid or alcohol, which dissolve but very little of the oil.

Commerce—Various sorts of olive oil are distinguished in the English market, as Florence, Gallipoli, Gioja, Spanish (Malaga and Seville), Sicily, Myteline, Corfu and Mogador.

Olive oil was imported into the United Kingdom in the year 1872 to the value of £1,193,064. Nearly half the quantity was shipped from Italy, one-fifth from Spain, and the remainder from other Mediterranean countries.

The average annual production in Italy is estimated at about 3 millions of hectolitres (66 million gallons), but the quantity exported does not reach half that amount.

The statistics of the French Government indicate the annual production of olive oil in France to be not more than 250,000 hectolitres, equivalent in value to 30 millions of francs (£1,200,000).

Uses—The uses of olive oil in medicine and its immense consumption in the warmer parts of Europe as an article of food, are too well known to require more than a passing allusion.

Adulteration—Olive Oil is the subject of various fraudulent admixtures with less costly oils, the means of detecting which has engaged much attention. Of the various methods by which chemists have endeavoured to ascertain the purity of olive oil, the following are the more noteworthy:—

a. Drying oils (such as the oils of poppy and walnut) may be distinguished by their not being converted into solid crystallizable elaidin by hyponitric acid or concentrated solution of nitrate of protoxide of mercury. Olive oil which contains any considerable proportion of one of these oils, no longer solidifies if exposed for a moment to one of the above-mentioned reagents. This test however is not of sufficient delicacy for small amounts of drying oils.

b. Olive oil being one of the lighter oils, the specific gravity may to some degree indicate admixture with a heavier oil. To make use of this fact, Gobley and other chemists have invented an instrument called an elaiometer, for taking the specific gravity of oils.

c. Observation of the Cohesion-figure.—This test, proposed by Tomlinson in 1864, depends on the forces of cohesion, adhesion, and diffusion. Thus, if a drop of any oil hanging from the end of a glass rod is gently deposited upon the surface of chemically clean water, contained in a clean glass, a contest takes place between the forces in question the moment the drop flattens down by its gravity upon the surface of the water. The adhesion of the liquid surface tends to spread out the drop into a film, the cohesive force of the particles of the drop strives to prevent that extension, and the resultant of these forces is a figure which Mr. Tomlinson believes to be definite for every independent liquid. The figure thus produced is named the cohesion-figure.

So far as our experience goes, the processes hitherto recommended for testing olive oil (and there are several that we have not mentioned) are only available in cases where the adulteration is considerable, and are quite insufficient for discovering a small admixture of other oils. How little they are appreciated, may be inferred from the fact that the Chamber of Commerce of Nice offered a reward of 15,000 francs (£600) for a simple and easy process for making evident an admixture with olive oil of 5 per cent. at least of any seed-oil.

Apocyneæ.

Cortex Alstoniæ.

Cortex Alstoniæ scholaris; Dita Bark; Alstonia Bark.

Botanical Origin—Alstonia scholaris R. Brown (Echites scholaris L.), a handsome forest tree, 50 to 90 feet in height, common throughout the Indian Peninsula from the sub-Himalayan region to Ceylon and Burma; found also in the Philippines, Java, Timor and Eastern Australia, likewise in Tropical Africa. It has oblong obovate leaves, in whorls of 5 to 7, and slender pendulous pods a foot or more in length.

History—Saptachhada and saptaparna (literally seven-leaf), occurring in early Sanskrit epic poetry and also in Susruta, are ancient names of Alstonia (Dr. Rice). Rheede in 1678 and Rumphius in 1741 described and figured the tree, and mentioned the use made of its bark by the native practitioners. Rumphius also explained the trivial name scholaris as referring to slabs of the close-grained wood which are used as school-slates, the letters being traced upon them in sand. The tonic properties of the bark were favourably spoken of by Graham in his Catalogue of Bombay Plants (1839), and further recommended by Dr. Alexander Gibson in 1853. The drug has a place in the Pharmacopœia of India, 1868.

Description—The drug, as presented to one of us by the late Dr. Gibson and by Mr. Broughton of Ootacamund, consists of irregular fragments of bark, ⅛ to ½ an inch thick, of a spongy texture, easily breaking with a short, coarse fracture. The external surface is very uneven and rough, dark grey or brownish, sometimes with blackish spots; the interior substance and inner surface (liber) is of a bright buff. A transverse section shows the liber to be finely marked by numerous small medullary rays. The bark is almost inodorous; its taste is purely bitter and neither aromatic nor acrid.

Microscopic Structure—The cortical tissue is covered with a thin suberous coat; the middle layer of the bark is built up of a thin walled parenchyme, through which enormous, hard, thick-walled cells are scattered in great numbers and are visible to the naked eye, as they form large irregular groups of a bright yellow colour. Towards the inner part these stone-cells disappear, the tissue being traversed by undulated medullary rays, loaded with very small starch grains; many of the other parenchymatous cells of the liber contain crystals of calcium oxalate. The longitudinal section of the liber exhibits large but not very numerous laticiferous vessels, containing a brownish mass, the concrete milk juice in which all parts of the tree abound.

Chemical Composition—The first attempts to isolate the active principles of this bark were made by two apothecaries, Scharlée at Batavia (1862) and Gruppe at Manila (1872).

In 1875 Jobst and Hesse exhausted the powdered bark with petroleum ether, and then extracted, by boiling alcohol, the salt of an alkaloid, which they called Ditamine. After the evaporation of the alcohol, it is precipitated by carbonate of sodium and dissolved by ether, from which it is removed by shaking it with acetic acid. Ditamine as again isolated from the acetate forms an amorphous and somewhat crystalline, bitterish powder of decidedly alkaline character; the barks yields about 0·02 per cent. of it.

From the substances extracted by means of petroleum ether, as above stated, Jobst and Hesse further isolated (1) Echicaoutchin, C₂₅H₄₀O₂, an amorphous yellowish mass; (2) Echicerin, C₃₀H₄₈O₂, forming acicular crystals, melting at 157° C.; (3) Echitin, C₃₂H₅₂O₂, crystallized scales, melting at 170°; (4) Echiteïn, C₄₂H₇₀O₂, which forms rhombic prisms, melting at 195°; (5) Echiretin, C₃₅H₅₆O₂, an amorphous substance melting at 52° C.

Echicaoutchin may be written thus: (C₅H₈)₅O₂, echicerin (C₅H₈)₆O₂, echiretin (C₅H₈)₇O₂; these formulæ at once point out how nearly the three last named substances are allied. They are probably constituents of the milky juice of the tree.

Lastly, Jobst and Hesse pointed out the existence of another alkaloid in Dita bark.

Harnack (1877) on the other hand is of the opinion that it contains only one alkaloid, which he terms Ditaïne. He used the alcoholic extract of the bark which he treated with ether to which he added a little ammonia. By this process ditamine of Jobst and Hesse would have been removed, but Harnack suggests that only a little ditaïne is dissolved by ether. He then mixed the extract with potash and exhausted it with alcohol, which afforded crystals of ditaïne, answering to the formula C₂₂H₃₀N₂O₄; its physiological action is nearly the same as that of curare. Ditaïne is but sparingly soluble in ether or petroleum ether, but dissolves readily in water, alcohol, or chloroform; it has a decidedly alkaline reaction. It would appear that it is a glucoside.

Dita bark is stated to yield 5 per cent. of “ditaïne”; but this probably refers not to the pure alkaloid.

Uses—The bark has been recommended as a tonic and antiperiodic, being extravagantly praised as a substitute for quinine.

Asclepiadeæ.

Radix Hemidesmi.

Hemidesmus Root, Nunnari Root, Indian Sarsaparilla.

Botanical Origin—Hemidesmus indicus R. Brown (Periploca indica Willd., Asclepias Pseudo-sarsa Roxb.), a twining shrub, growing throughout the Indian Peninsula and in Ceylon. The leaves are very diverse, being narrow and lanceolate in the lower part of the plant, and broadly ovate in the upper branches.

History—In the ancient Sanskrit literature the plant occurs frequently under the name Sārivā, and its root under the name of Nannārī or Ananta-mūl (i.e. endless root) has long been employed in medicine in the southern parts of India. Ashburner in 1831 was the first to call the attention of the profession in Europe to its medicinal value. In 1864 it was admitted to a place in the British Pharmacopœia, but its efficiency is by no means generally acknowledged.

Description—The root is in pieces of 6 inches or more in length; it is cylindrical, tortuous, longitudinally furrowed, from ²/₁₀ to ⁷/₁₀ of an inch in thickness, mostly simple or provided with a few thin rootlets emitting slender, branching woody aerial stems, ³/₀ of an inch or less thick. Externally it is dark brown, sometimes with a slight violet-grey hue, which is particularly obvious in the sunshine. The transverse section of the hard root shows a white mealy or brownish or somewhat violet cortical layer, not exceeding ⅒ of an inch in thickness, and a yellowish woody column, separated by a narrow dark undulated cambial line. Neither the wood nor the cortical tissue present a radiate structure in the stout pieces; in the thinner roots, medullary rays are obvious in the woody part. The extremely thin corky layer easily separates from the bark, which latter is frequently marked transversely by large cracks. The root, whether fresh or dried, has an agreeable odour resembling tonka bean or melilot. The dried root has a sweetish taste with a very slight acidity. The stems are almost tasteless and inodorous. The root found in the English market is often of very bad quality.

Microscopic Structure—All the proper cortical tissue shows a uniform parenchyme, not distinctly separated into liber, medullary rays and mesophlœum. On making a longitudinal section however, one can observe some elongated laticiferous vessels filled with the colourless concrete milky juice. In a transverse section, they are seen to be irregularly scattered through the bark, chiefly in its inner layers, yet even here in not very considerable number. They are frequently 30 mkm. in diameter and not branched.

The wood is traversed by small medullary rays, which are obvious only in the longitudinal section. The parenchymatous tissue of the root is loaded with large, ovoid starch granules. Tannic matters do not occur to any considerable amount, except in the outermost suberous layer.

Chemical Composition—The root has not been submitted to any adequate chemical examination. Its taste and smell appear not to depend on the presence of essential oil, so far as may be inferred from microscopic examination; and it is probable the aroma is due to a body of the cumarin class. According to Scott, the root yields by simple distillation with water a stearoptene, which is probably the substance obtained by Garden in 1837, and supposed to be a volatile acid.

Uses—The drug is reputed to be alterative, tonic, diuretic and diaphoretic, but is rarely employed, at least in England.

Cortex Mudar.

Cortex Calotropidis; Mudar; F. Ecorce de racine de Mudar.

Botanical Origin—The drug under notice is furnished by two nearly allied species of Calotropis, occupying somewhat distinct geographical areas, but not distinguished from each other in the native languages of India. These plants are:—

1. Calotropis procera R. Brown (C. Hamiltonii Wight), a large shrub, 6 or more feet high, with dark green, oval leaves, downy beneath, abounding in acrid milky juice.

It is a native of the drier parts of India, as the Deccan, the Upper Provinces of Bengal, the Punjab and Sind, but is quite unknown in the southern provinces; it also extends to Persia, Palestine, the Sinaitic Peninsula, Arabia, Egypt, to the oasis Dachel, and other oases of the Sahara, to Nubia, Abyssinia, the lake Tsad and through the Sudan. Lastly it has been naturalized in the West Indies.

2. C. gigantea R. Brown (Asclepias gigantea Willd.), a large erect shrub, 6 to 10 feet high, with stem as thick as a man’s leg, much resembling preceding, indigenous to Lower Bengal and the southern parts of India, Ceylon, the Malayan Peninsula, and the Moluccas.

Both species are extremely common in waste ground over their respective areas.

History—The ancient name of the plant, which occurs already in the Vedic literature, was Arka (wedge), alluding to the form of the leaves which were used in sacrificial rites. From one of the Sanskrit names of this plant, namely Mandāra, Mudar is a corruption; the latter is frequently mentioned in the writings of Susruta.

The plant was likewise well known to the Arabian physicians.

C. procera was observed in Egypt by Prosper Alpinus (1580-84), and upon his return to Italy was figured, and some account given of its medicinal properties. It is also the “Apocynum syriacum” figured by Clusius.

C. gigantea was figured by Rheede in 1679, and in our own day by Wight.

The medicinal virtues of mudar, though so long esteemed by the natives of India, were not investigated experimentally by Europeans until the present century, when Playfair recommended the drug in elephantiasis, and its good effects were afterwards noticed by Vos (1826), Cumin (1827), and Duncan (1829). The last named physician also performed a chemical examination of the root-bark, the activity of which he referred to an extractive matter which he termed Mudarine.

Description—The root-bark of C. procera, as we have received it, consists of short, arched, bent, or nearly flat fragments, ⅛ to ⅕ of an inch thick. They have outwardly a thickish, yellowish-grey, spongy cork, more or less fissured lengthwise, frequently separating from the middle cortical layer; the latter consists of a white mealy tissue, traversed by narrow brown liber-rays. The bark is brittle and easily powdered; it has a mucilaginous, bitter, acrid taste, but no distinctive odour. The light yellow, fibrous wood is still attached to many of the pieces.

The roots of C. gigantea are clothed with a bark which seems to be undistinguishable from that of C. procera just described. The wood of the root consists of a porous, pale yellow tissue, exhibiting large vascular bundles, and very numerous small medullary rays, consisting of 1 to 3 rows of the usual cells.

Microscopic Structure—In the root-bark of C. procera, the suberous coat is made up of large, thin-walled, polyhedral, or almost cubic cells; the middle cortical layer, of a uniform parenchyme, loaded with large starch granules, or here and there containing some thick-walled cells (sclerenchyme) and tufts of oxalate of calcium. The large medullary rays are built up of the usual cells, having porous walls and containing starch and oxalate. In a longitudinal section, the tissue, chiefly of the middle cortical layer, is found to be traversed by numerous laticiferous vessels, containing the dry milk juice as a brownish granular substance not soluble in potash.

The microscopic characters of the root-bark of C. gigantea agree with those here detailed of C. procera. The stems of Calotropis are distinguished by strong liber-fibres, which are not met with in the roots.

Chemical Composition—By following the process of Duncan above alluded to, 200 grammes of the powdered bark of C. gigantea yielded us nothing like his Mudarine, but 2·4 grammes of an acrid resin, soluble in ether as well as in alcohol. The latter solution reddens litmus; the former on evaporation yields the resin as an almost colourless mass. If the aqueous liquid is separated from the crude resin, and much absolute alcohol added, an abundant precipitate of mucilage is obtained. The liquid now contains a bitter principle, which after due concentration may be separated by means of tannic acid.

We obtained similar results by exhausting the bark of C. procera with dilute alcohol. The tannic compound of the bitter principle was mixed with carbonate of lead, dried and boiled with spirit of wine. This after evaporation furnished an amorphous, very bitter mass, not soluble in water, but readily so in absolute alcohol. The solution is not precipitated by an alcoholic solution of acetate of lead. By purifying the bitter principle with chloroform or ether, it is at last obtained colourless. This bitter matter is probably the active principle of Calotropis; we ascertained by means of the usual tests that no alkaloid occurs in the drug. The large juicy stem, especially that of C. gigantea, ought to be submitted to an accurate chemical and therapeutical examination.

Uses—Mudar is an alterative, tonic and diaphoretic,—in large doses emetic. By the natives of India, who employ it in venereal and skin complaints, almost all parts of the plant are used. According to Moodeen Sheriff, the bark of the root and the dried milky juice are the most efficient; the latter is however somewhat irregular and unsafe in its action. The same writer remarks that he has found that the older the plant, the more active is the bark in its effects. He recommends that the corky outer coat, which is tasteless and inert, should be scraped off before the bark is powdered for use: of a powder so prepared, 40 to 50 grains suffice as an emetic.

The stems of C. gigantea afford a very valuable fibre which can be spun into the finest thread for sewing or weaving.

Folia Tylophoræ.

Country or Indian Ipecacuanha.

Botanical Origin—Tylophora asthmatica Wight et Arnott (Asclepias asthmatica Roxb.), a twining perennial plant, common in sandy soils throughout the Indian Peninsula and naturalized in Mauritius. It may be distinguished from some of its congeners by its reddish or dull pink flowers, with the scale of the staminal corona abruptly contracted into a long sharp tooth.

History—The employment of this plant in medicine is well known to the Hindus, who call it Antamul and use it with considerable success in dysentery, but we have not succeeded in tracing it in the ancient Indian literature. During the last century it attracted the attention of Roxburgh who made many observations on the administration of the root, while physician to the General Hospital of Madras from 1776 to 1778. It was also used very successfully in the place of ipecacuanha by Anderson, Physician-General to the Madras army. In more recent times, the plant has been prescribed by O’Shaughnessy, who pronounced the root an excellent substitute for ipecacuanha if given in rather larger doses. Kirkpatrick administered the drug in at least a thousand cases, and found it of the greatest value; he prescribed the dried leaf, not only because superior to the root in certainty of action, but also as being obtainable without destruction of the plant. The drug has been largely given by many other practitioners in India. Tylophora is also employed in Mauritius, where it is known as Ipéca sauvage or Ipéca du pays. It has a place in the Bengal Pharmacopœia of 1844, and in the Pharmacopœia of India of 1868.

Description—The leaves are opposite, entire, from 2 to 5 inches long, ¾ to 2½ inches broad, somewhat variable in outline, ovate or subrotund, usually cordate at the base, abruptly acuminate or almost mucronate, rather leathery, glabrous above, more or less downy beneath with soft simple hairs. The pedicel, which is channelled, is ½ to ¾ of an inch in length. In the dry state the leaves are rather thick and harsh, of a pale yellowish green; they have a not unpleasant herbaceous smell, with but very little taste.

Chemical Composition—A concentrated infusion of the leaves has a slightly acrid taste. It is abundantly precipitated by tannic acid, by neutral acetate of lead or caustic potash, and is turned greenish-black by perchloride of iron. Broughton of Ootacamund (India) has informed us (1872) that from a large quantity of the leaves he obtained a small amount of crystals,—insufficient for analysis. Dissolved and injected into a small dog, they occasioned purging and vomiting.

Uses—Employed in India, as already mentioned, as a substitute for ipecacuanha, chiefly in the treatment of dysentery. The dose of the powdered leaves as an emetic is 25 to 30 grains, as a diaphoretic and expectorant 3 to 5 grains.

Radix Tylophoræ—This root is met with in the Indian bazaars, and has been employed, as before stated, as much or more than the leaf. It consists of a short, knotty, descending rootstock, about ⅛ of an inch in thickness, emitting 2 to 3 aerial stems, and a considerable number of wiry roots. These roots are often 6 inches or more in length by ½ a line in diameter, and are very brittle. The whole drug is of a pale yellowish-brown; it has no considerable odour, but a sweetish and subsequently acrid taste. In general appearance it is suggestive of valerian, but is somewhat stouter and larger.

Examined microscopically, the parenchymatous envelope of the rootlets is seen to consist of two layers, the inner forming a small nucleus sheath. The outer portion is built up of large cells, loaded with starch granules and tufted crystals of oxalate of calcium. Salts of iron do not alter the tissue.

Loganiaceæ.

Nux Vomica.

Semen Nucis Vomicæ; Nux Vomica; F. Noix vomique; G. Brechnuss.

Botanical Origin—Strychnos Nux vomica L., a moderate sized tree with short, thick, often crooked stem, and small, greenish-white, tubular flowers ranged in terminal corymbs. It is indigenous to most parts of India, especially the coast districts, and is found in Burmah, Siam, Cochin China and Northern Australia.

The ovary of S. Nux vomica is bilocular, but as it advances in growth the dissepiment becomes fleshy and disappears. The fruit, which is an indehiscent berry of the size and shape of a small orange, is filled with a bitter, gelatinous white pulp, in which the seeds, 1 to 5 in number, are placed vertically in an irregular manner. The epicarp forms a thin, smooth, somewhat hard shell, which at first is greenish, but when mature, of a rich orange-yellow. The pulp of the fruit contains strychnine, yet it is said to be eaten in India by birds. The wood, which is hard and durable, is very bitter.

History—Nux Vomica, which was unknown to the ancients, is thought to have been introduced into medicine by the Arabians. But the notices in their writings which have been supposed to refer to it, are far from clear and satisfactory. We have no evidence moreover that it was used in India at an early period. Garcia de Orta, an observer thoroughly acquainted with the drugs of the west coast of India in the middle of the 16th century, is entirely silent as to nux vomica. Fleming, writing at the beginning of the present century, remarks that nux vomica is seldom, if ever, employed in medicine by the Hindus, but this statement does not hold good now.

The drug was however certainly made known in Germany in the 16th century. Valerius Cordus wrote a description of it about the year 1540, which is remarkable for its accuracy. Fuchs, Bauhin and others noticed it as Nux Metella, a name taken from the Methel of Avicenna and other Arabian authors.

It was found in the English shops in the time of Parkinson (1640), who remarks that its chief use is for poisoning dogs, cats, crows, and ravens, and that it is rarely given as a medicine.

Description—Nux Vomica is the seed, removed from the pulp and shell. It is disc-like, or rather irregularly orbicular, a little less than an inch in diameter, by about a quarter of an inch in thickness, slightly concave on the dorsal, convex on the ventral surface, or nearly flat on either side, often furnished with a broad, thickened margin so that the central portion of the seed appears depressed. The outside edge is rounded or tapers into a keel-like ridge. Each seed has on its edge a small protuberance, from which is a faintly projecting line (raphe) passing to a central scar, which is the hilum or umbilicus; a slight depression marks the opposite side of the seed. The seeds are of a light greyish hue, occasionally greenish, and have a satiny or glistening aspect, by reason of their being thickly covered with adpressed, radiating hairs. Nux vomica is extremely compact and horny, and has a very bitter taste.

After having been softened by digestion in water, the seed is easily cut along its outer edge, then displaying a mass of translucent, cartilaginous albumen, divided into two parts by a fissure in which lies the embryo. This latter is about ³/₁₀ of an inch long, having a pair of delicate 5-to 7-nerved, heart-shaped cotyledons, with a club-shaped radicle, the position of which is indicated on the exterior of the seed by the small protuberance already named.

Microscopic Structure—The hairs of nux vomica are of remarkable structure. They are formed as usual of the elongated cells of the epidermis, and have their walls thickened by secondary deposits, which are interrupted by longitudinally extended pores; they are a striking object in polarized light. The albumen is made up of large cells, loaded with albuminoid matters and oily drops, but devoid of starch. In water the thick walls of this parenchyme swell up and yield some mucilage; the cotyledons are built up of a narrow, much more delicate tissue, traversed by small fibro-vascular bundles.

The alkaloids are not directly recognizable by the microscope; but if very thin slices of nux vomica are kept for some length of time in glycerin, they develop feathery crystals, doubtless consisting of these bases.

Chemical Composition—The bitter taste and highly poisonous action of nux vomica are chiefly due to the presence of Strychnine and Brucine. Strychnine, C₂₁H₂₂N₂O₂, was first met with in 1818 by Pelletier and Caventou in St. Ignatius’ Beans, and immediately afterwards in nux vomica. It crystallizes from an alcoholic solution in large anhydrous prisms of the orthorhombic system. It requires for solution about 6700 parts of cold or 2500 of boiling water; the solution is of decidedly alkaline reaction, and an intensely bitter taste which may be distinctly perceived though it contain no more than ¹/₆₀₀₀₀₀ of the alkaloid. The best solvents for strychnine are spirit of wine or chloroform; it is but very sparingly soluble in absolute alcohol, benzol, amylic alcohol, or ether. The alcoholic solution deviates the ray of polarized light to the left.

Strychnine is not restricted to the fruit of the plant under notice, but also occurs in the wood and bark. It is moreover found in the wood of the root of Strychnos colubrina L., and in the bark of the root of Strychnos Tieute Lesch., both species indigenous to the Indian Archipelago.

The discovery of Brucine was made in 1819 by the same chemists, in nux vomica bark, then supposed to be derived from Brucea ferruginea Héritier (B. antidysenterica Miller), an Abyssinian shrub of the order Simarubeæ. The presence of brucine in nux vomica and St. Ignatius’ Bean was pointed out by them in 1824. Brucine, dried over sulphuric acid, has the formula C₂₃H₂₆N₂O₄, but it crystallizes from its alcoholic solution with 4 OH₂. In bitterness and poisonous properties, as well as in rotatory power, it closely resembles strychnine, differing however in the following particulars:—it is soluble in about 150 parts of boiling water, melts without alteration a little above 130° C. In common with its salts, it acquires a dark red colour when moistened with concentrated nitric acid.

The proportion of strychnine in nux vomica appears to vary from ¼ to ½ per cent. That of brucine is variously stated to be 0·12 (Merck), 0·5 (Wittstein), 1·01 (Mayer) per cent.

A third crystallizable base, called Igasurine, was stated in 1853 by Desnoix to occur in the liquors from which strychnine and brucine had been precipitated by lime. Schützenberger’s investigations (1858) are far from proving the existence of “igasurine.”

In nux vomica, as well as in St. Ignatius’ Beans, the alkaloids, according to their discoverers, are combined with Strychnic or Igasuric Acid; Ludwig (1873), who prepared this body from the latter drug, describes it as a yellowish-brown amorphous mass, having a strongly acid reaction and a sour astringent taste, and striking a dark green with ferric salts. We have ascertained the correctness of Ludwig’s observations.

Nux vomica dried at 100° C. yielded us when burnt with soda-lime 1·822 per cent. of nitrogen, indicating about 11·3 per cent. of protein substances. By boiling ether, we removed from the seeds 4·14 per cent. of fat; Meyer found it to yield butyric, capronic, caprylic, caprinic and other acids of the series of the common fatty acids, and also one acid richer in carbon than stearic acid. Nux vomica also contains mucilage and sugar. The latter, which according to Rebling (1855) exists to the extent of 6 per cent., reduces cupric oxide without the aid of heat. When macerated in water, the seeds easily undergo lactic fermentation, not however attended with decomposition of the alkaloids. The stability of strychnine is remarkable, even after ten years of contact with putrescent animal substances.

Commerce—Large quantities of nux vomica are brought into the London market from British India. The export from Bombay in the year 1871-72 was 3341 cwt., all shipped to the United Kingdom. Madras in 1869-70 exported 4805 cwt.; and Calcutta in 1865-66, 2801 cwt. The quantity imported into the United Kingdom in 1870 was 5534 cwt.

Nux vomica is stated by Garnier (l.c. page 429, note) to be largely exported from Cambodja to China.

Uses—Tincture and extract of nux vomica, and the alkaloid strychnine, are frequently administered as tonic remedies in a variety of disorders.

Semen Ignatii.

Faba Sancti Ignatii; St. Ignatius’ Beans; F. Fèves de Saint Ignace, Noix Igasur; G. Ignatiusbohnen.

Botanical Origin—Strychnos Ignatii Bergius (S. philippensis Blanco, Ignatiana philippinica Loureiro), a large climbing shrub, growing in Bohol, Samar, and Çebu, islands of the Bisaya group of the Philippines, and according to Loureiro in Cochin China, where it has been introduced. The inflorescence and foliage are known to botanists only from the descriptions given by Loureiro and Blanco. The fruit is spherical, or sometimes ovoid, 4½ inches in diameter by 6¾ long, as shown by Ray and Petiver’s figure. It has a smooth brittle shell enclosing seeds to the number of about 24. G. Bennett, who saw the fruits at Manila sold in the bazaar, says they contain from 1 to 12 seeds, imbedded in a glutinous blackish pulp. According to Jagor the shrub is abundant near Basey, in the south-western part of the island of Samar, on the straits of San Juanico; its seeds are met with as a medicine in many houses in the Philippines.

History—It is stated by Murray and later writers that this seed was introduced into Europe from the Philippines by the Jesuits, who, on account of its virtues, bestowed upon it the name of Ignatius, the founder of their order. However this may be, the earliest account of the drug appears to be that communicated by Camelli, Jesuit missionary at Manila, to Ray and Petiver, and by them laid before the Royal Society of London in 1699. Camelli proclaimed the seed to be the Nux Vomica legitima of the Arabian physician Serapion, who flourished in the 9th century; but in our opinion there is no warrant whatever for supposing it to have been known at so remote a period. Sancti Ignatii, is much esteemed as a remedy in various disorders, though he was well aware of its poisonous properties when too freely administered. In Germany, St. Ignatius’ Bean was made known about the same period by Bohn of Leipzig.

The drug is found in the Indian bazaars under a name which is evidently corrupted from the Spanish pepita. It is met with in the drugshops of China as Leu-sung-kwo, i.e. Luzon fruit.

Description—St. Ignatius’ Beans are about an inch in length; their form is ovoid, yet by mutual pressure it is rendered very irregular, and they are 3-, 4-, or 5-sided, bluntly angular, or flattish, with a conspicuous hilum at one end. In the fresh state, they are covered with silvery adpressed hairs: portions of a shaggy brown epidermis are here and there perceptible on those found in commerce, but in the majority the seed shows the dull grey, granular surface of the albumen itself.

Notwithstanding the different outward appearance, the structure of St. Ignatius’ Beans accords with that of nux vomica. The radicle however is longer, thicker, and frequently somewhat bent, and the cotyledons are more pointed. The horny brownish albumen is translucent, very hard, and difficult to split. The whole seed swells considerably by prolonged digestion in warm water, and has then a heavy, earthy smell. The beans are intensely bitter and highly poisonous.

Microscopic Structure—The hairs of the epidermis are of an analogous structure, but more simple than in nux vomica. The albumen and cotyledons agree in structural features with those of the same parts in nux vomica.

Chemical Composition—Strychnine exists to the extent of about 1·5 per cent.; the seeds also contain 0·5 per cent. of brucine. Dried over sulphuric acid and burnt with soda-lime, it yielded us an average of 1·78 per cent. of nitrogen, which would answer to about 10 per cent. of albuminoid matter.

Commerce—We have no information as to the collection of the drug. The seeds are met with irregularly in English trade, being sometimes very abundant, at others scarcely obtainable.

Uses—The same as those of nux vomica. When procurable at a moderate price, the seeds are valued for the manufacture of strychnine.

Radix Spigeliæ.

Radix Spigeliæ Marilandicæ; Indian Pink Root, Carolina Pink Root, Spigelia.

Botanical Origin—Spigelia marilandica L., an herbaceous plant about a foot high, indigenous in the woods of North America, from Pennsylvania to Wisconsin and southward. According to Wood and Bache, it is collected chiefly in the Western and South-western States.

History—The anthelminthic properties of the root, discovered by the Indians, were brought to notice in Europe about the year 1754 by Linning, Garden, and Chalmers, physicians of Charleston, South Carolina. The drug was admitted to the London Pharmacopœia in 1788.

Description—Pink root has a near resemblance to serpentary, consisting of a short, knotty, dark brown rhizome emitting slender wiry roots. It is quite wanting in the peculiar odour of the latter drug, or indeed in any aroma; in taste it is slightly bitter and acrid. Sometimes the entire plant with its quadrangular stems a foot high is imported. It has opposite leaves about 3 inches long, sessile, ovate-lanceolate, acuminate, smooth or pubescent.

Microscopic Structure—The transverse section of the rhizome, about ²/₁₀ of an inch in diameter, shows a small woody zone enclosing a large pith of elliptic outline, consisting of thin-walled cells. Usually the central tissue is decayed. In the roots, the middle cortical layer predominates; it swells in water, after which its large cells display fine spiral markings. The nucleus-sheath observable in serpentary is wanting in spigelia.

Chemical Composition—Not satisfactorily known: the vessels of the wood contain resin, the parenchyme starch; in the cortical part of the rhizome some tannic matters occur, but not in the roots. Feneulle (1823) asserts that the drug yields a little essential oil. The experiments of Bureau show that spigelia acts on rabbits and other animals as a narcotico-acrid poison.

Uses—Spigelia has long been reputed a most efficient medicine for the expulsion of Ascaris lumbricoides, but according to Stillé, its real value for this purpose has probably been over-estimated. This author speaks of it as possessing alterative and tonic properties. In England, it is rarely prescribed by the regular practitioner, but is used as a household medicine in some districts. It is much employed in the United States.

Gentianeæ.

Radix Gentianæ.

Gentian Root; F. Racine de Gentiane; G. Enzianwurzel.

Botanical Origin—Gentiana lutea L., a handsome perennial herb, growing 3 feet high, indigenous to open grassy places on the mountains of Middle and Southern Europe. It occurs in Portugal, Spain, the Pyrenees, in the islands of Sardinia and Corsica, in the Apennines, the mountains of Auvergne, the Jura, the Vosges, the Black Forest, and throughout the chain of the Alps as far as Bosnia and the Danubian Principalities. Among the mountains of Germany, it is found on the Suabian Alps near Würzburg, and here and there in Thuringia, but not further north, nor does it occur in the British Islands.

History—The name Gentiana is said to be derived from Gentius, a king of the Illyrians, living b.c. 180-167, by whom, according to both Pliny and Dioscorides, the plant was noticed. Whether the species thus named was Gentiana lutea is doubtful. During the middle ages, gentian was commonly employed for the cure of disease, and as an antidote to poison. Tragus in 1552 mentions it as a means of diluting wounds, an application which has been resorted to in modern medical practice.

Description—The plant has a cylindrical, fleshy, simple root, of pale colour, occasionally almost as much as 4 feet in length by 1½ inches in thickness, producing 1 to 4 aerial stems.

The dried root of commerce is in irregular, contorted pieces, several inches in length, and ½ to 1 inch in thickness; the pieces are much wrinkled longitudinally, and marked transversely, especially in their upper portion, with numerous rings. Very often they are split to facilitate drying. They are of a yellowish-brown; internally of a more orange tint, spongy, with a peculiar, disagreeable, heavy odour, and intensely bitter taste. The crown of the root, which is somewhat thickened, is clothed with the scaly bases of leaves. The root is tough and flexible,—brittle only immediately after drying. We found it to lose in weight about 18 per cent.; by complete drying in a water-bath it regained 16 per cent. by being afterwards exposed to the air.

Microscopic Structure—A transverse section shows the bark separated by a dark cambial zone from the central column; the radial arrangement of the tissues is only obvious in the latter part. In the bark, liber-fibres are wanting; and in the centre there is no distinct pith. The fibro-vascular bundles are devoid of thick-walled ligneous prosenchyme; this may explain the consistence, and the short even fracture of the root. It is moreover remarkable on account of the absence both of starch and oxalate of calcium; the cells appear to contain chiefly sugar and a little fat oil.

Chemical Composition—The bitter taste of gentian is due to a substance called Gentiopicrin or Gentian-bitter, C₂₀H₃₀O₁₂. Several chemists, as Henry, Caventou, Trommsdorff, Leconte and Dulk have described the bitter principle of gentian in an impure state, under the name of Gentianin, but Kromayer in 1862 first obtained it in a state of purity. Gentiopicrin is a neutral body crystallizing in colourless needles, which readily dissolve in water. It is soluble in spirit of wine, but in absolute alcohol only when aided by heat; it does not dissolve in ether. A solution of caustic potash or soda forms with it a yellow solution. Under the influence of a dilute mineral acid, gentiopicrin is resolved into glucose, and an amorphous, yellowish-brown, neutral substance, named Gentiogenin. Fresh gentian roots yield somewhat more than ⅒ per cent. of gentiopicrin; from the dried root it could not be obtained in a crystallized state. The medicinal Tincture of Gentian, mixed with solution of caustic potash, loses its bitterness in a few days, probably in consequence of the destruction of the gentiopicrin.

Another constituent of gentian root is Gentianin or gentisin

CH₃

C₁₄H₁₀O₅ or (OH)₂C₆H₃·CO·C₆H₂ O \ .

O /

It forms tasteless yellowish prisms, sparingly soluble in alcohol, requiring about 5000 parts of water for solution. With alkalis it yields intensely yellow crystallizable compounds, which, however, are easily decomposed already by carbonic acid. Gentianin may be sublimed if carefully heated at 250° C. By melting it with caustic potash, acetic acid, phloroglucin, C₆H₃(OH)₃, and oxysalicylic acid, C₆H₃(OH)₂COOH, are produced, as shown in 1875 by Hlasiwetz and Habermann. The name of gentianic acid or gentisinic acid had been applied to the oxysalicylic acid obtained by the above decomposition before it was identified with oxysalicylic acid from other sources.

Gentian root abounds in pectin; it also contains, to the extent of 12 to 15 per cent., an uncrystallizable sugar, of which advantage is taken in Southern Bavaria and Switzerland for the manufacture by fermentation and distillation of a potable spirit. This use of gentian and its consumption in medicine have led to the plant being almost extirpated in some parts of Switzerland where it formerly abounded.

The experiments of Maisch (1876) and Ville (1877) have shown tannic matters to be absent from the root.

Commerce—Gentian root finds its way into English commerce through the German houses; and some is shipped from Marseilles. The quantity imported into the United Kingdom in 1870 was 1100 cwt.

Uses—Gentian is much used in medicine as a bitter tonic. Ground to powder, the root is an ingredient in some of the compositions sold for feeding cattle.

Substitutes—It can hardly be said that gentian is adulterated, yet the roots of several other species possessing similar properties are occasionally collected; of these we may name the following:—

1. Gentiana purpurea L.—This species is found in Alpine meadows of the Apennines, Savoy and Switzerland, in Transylvania, and in South-western Norway; a variety also in Kamtchatka. The root is frequently collected; it attains at most 18 inches in length and a diameter of about 1 inch at the summit, from which arise 8 to 10 aerial stems, clothed below with many scaly remains of leaves. The top of the root has thus a peculiar branched appearance, never found in the root of G. lutea, with which in all other respects that of G. purpurea agrees. The latter is perhaps even more intensely bitter.

2. G. punctata L.—Nearly the same description applies to this species, which is a native of the Alps of South-Eastern France, Savoy, the southern parts of Switzerland, extending eastward to Austria, Hungary and Roumelia.

3. G. pannonica Scop.—a plant of the mountains of Austria, unknown in the Swiss Alps, has a root which does not attain the length or the thickness of the root of G. purpurea, with which it agrees in other respects. It is officinal in the Austrian Pharmacopœia.

4. G. Catesbœi Walter (G. Saponaria L.)—indigenous in the United States. Its root, usually not exceeding 3 inches in length by ⅓ inch in diameter, has a very thin woody column within a spongy whitish cortical tissue and a bright yellow epidermis. This root is less bitter than the above enumerated drugs; the same remark applies also to those European Gentianæ which like G. Catesbœi are provided with blue flowers.

Herba Chiratæ.

Herba Chirettæ vel Chiraytæ; Chiretta or Chirayta.

Botanical Origin—Ophelia Chirata Grisebach (Gentiana Chirayita Roxb.), an annual herb of the mountainous regions of Northern India from Simla through Kumaon to the Murung district in South-eastern Nepal.

History—Chiretta has long been held in high esteem by the Hindus, and is frequently mentioned in the writings of Susruta. It is called in Sanscrit Kirāta-tikta, which means the bitter plant of the Kirātus, the Kirātas being an outcast race of mountaineers in the north of India. In England, it began to attract some attention about the year 1829; and in 1839 was introduced into the Edinburgh Pharmacopœia. The plant was first described by Roxburgh in 1814.

Chiretta was regarded by Guibourt as the Calamus aromaticus of the ancients, but the improbability of this being correct was well pointed out by Fée and by Royle, and is now generally admitted.

Description—The entire plant is collected when in flower, or more commonly when the capsules are fully formed, and tied up with a slip of bamboo into flattish bundles of about 3 feet long, each weighing when dry from 1½ to 2 lb. The stem, ²/₁₀ to ³/₁₀ of an inch in thickness, is of an orange-brown, sometimes of a dark purplish colour; the tapering simple root, often much exceeding the stem in thickness, is 2 to 4 inches long and up to ½ an inch thick. It is less frequently branched, but always provided with some rootlets. In stronger specimens, the root is somewhat oblique or geniculate; perhaps the stem is in this case the product of a second year’s growth and the plant not strictly annual. Each plant usually consists of a single stem, yet occasionally two or more spring from a single root. The stem rises to a height of 2 to 3 feet, and is cylindrical in its lower and middle portion, but bluntly quadrangular in its upper, the four edges being each marked with a prominent decurrent line, as in Erythræa Centaurium and many other plants of the order. The decussate ramification resembles that of other gentians; its stems are jointed at intervals of 1½ to 3 or 4 inches, bearing opposite semi-amplexicaul leaves on their cicatrices. The stem consists in its lower portion of a large woody column, coated with a very thin rind, and enclosing a comparatively large pith. The upper parts of the stem and branches contain a broad ring of thick-walled woody parenchyme. The numerous slender axillary and opposite branches are elongated, and thus constitute a dense umbellate panicle. They are smooth and glabrous, of a greenish or brownish grey colour.

The leaves are ovate-acuminate, cordate at the base, entire, sessile, the largest 1 inch or more in length, 3-to 5-or 7-nerved, the midrib being strongest. At each division of the panicle there are two small bracts. The yellow corolla is rotate, 4-lobed, with glandular pits above the base; the calyx is one-third the length of the petals, which are about half an inch long. The one-celled, bivalved capsule contains numerous seeds.

The flowers share the intense bitterness of the whole drug. The wood of stronger stems is devoid of the bitter principles.

Chemical Composition—A chemical examination of chiretta has been made at our request under the direction of Professor Ludwig of Jena, by his assistant Mr. Höhn. The chief results of this careful and elaborate investigation may be thus described.

Among the bitter principles of the drug, Ophelic Acid, C₁₃H₂₀O₁₀, occurs in the largest proportion. It is an amorphous, viscid, yellow substance, of an acidulous, persistently bitter taste, and a faint gentian-like odour. With basic acetate of lead, it produces an abundant yellow precipitate. Ophelic acid does not form an insoluble compound with tannin; it dissolves in water, alcohol and ether. The first solution causes the separation of protoxide of copper from an alkaline tartrate of that metal.

A second bitter principle, Chiratin, C₂₆H₄₈O₁₅, may be removed by means of tannic acid, with which it forms an insoluble compound. Chiratin is a neutral, not distinctly crystalline, light yellow, hygroscopic powder, soluble in alcohol, ether and in warm water. By boiling hydrochloric acid, it is decomposed into Chiratogenin, C₁₃H₂₄O₃, and ophelic acid. Chiratogenin is a brownish, amorphous substance, soluble in alcohol but not in water, nor yielding a tannic compound. No sugar is formed in this decomposition.

These results exhibit no analogy to those obtained in the analysis of the European gentians. Finally, Höhn remarked in chiretta a crystallizable, tasteless, yellow substance, but its quantity was so minute that no investigation of it could be made.

The leaves of chiretta, dried at 100° C., afforded 7·5 per cent. of ash; the stems 3·7; salts of potassium and calcium prevailing in both.

Uses—Chiretta is a pure bitter tonic, devoid of aroma and astringency. In intense bitterness it exceeds gentian, Erythræa and other European plants of the same order. It is much valued in India, but is not very extensively used in England, and not at all on the Continent. It is said to be employed when cheap, in place of gentian, to impart flavour to the compositions now sold as Cattle Foods.

Substitutes and Adulteration—Some other species of Ophelia, namely, O. angustifolia Don, O. densifolia Griseb., O. elegans Wight, O. pulchella Don, and O. multiflora Dalz, two or three species of Exacum, besides Andrographis paniculata Wall., are more or less known in the Indian bazaars by the name of Chiretta and possess to a greater or less degree the bitter tonic properties of that drug. Another Gentianacea, Slevogtia orientalis Griseb., is called Chota Chiretta, i.e. small chiretta. It would exceed due limits were we to describe each of these plants: we have therefore given a somewhat detailed description of the true chiretta, which will suffice for its identification. We have frequently examined the chiretta found in the English market, but have never met with any other than the legitimate sort. Bentley noticed in 1874 the substitution of Ophelia angustifolia, which he found to be by far less bitter than true chiretta.

Convolvulaceæ.

Scammonium.

Scammony; F. Scammonée; G. Scammonium.

Botanical Origin—Convolvulus Scammonia L., a twining plant much resembling the common C. arvensis of Europe, but differing from it in being of larger size, and having a stout tap-root. It occurs in waste bushy places in Syria, Asia Minor, Greece, the Greek Islands, extending northward to the Crimea and Southern Russia, but appears to be wanting in Northern Africa, Italy, and in all the western parts of the Mediterranean basin.

History—The dried milky juice of the scammony plant has been known as a medicine from very ancient times. Theophrastus in the 3rd century b.c. was acquainted with it; it was likewise familiar to Dioscorides, Pliny, Celsus, and Rufus of Ephesus, each of whom has given some account of the manner in which it was collected. Scammony used then also to be called Diagrydion, from the Greek word δάκρυ, tear. The mediæval Arabian physicians also knew scammony and the plant from which it is derived. The drug was used in Britain in the 10th and 11th centuries, and would appear to be one of the medicines recommended to King Alfred the Great, by Helias, patriarch of Jerusalem. It is repeatedly named in the medical writings in use prior to the Norman conquest (a.d. 1066), in one of which directions are given for recognizing the goodness of the drug by the white emulsion it produces when wetted.

The botanists of the 16th and 17th centuries, as Brunfels, Gesner, Matthiolus, Dodonæus, and the Bauhins, described and figured the plant partly under the name of Scammonia syriaca. The collecting of the drug was well described by Russell, an English physician of Aleppo (1752), whose account is accompanied by an excellent figure representing the plant and the means of obtaining its juice.

Scammony was formerly distinguished by the names Aleppo and Smyrna, the former sort being twice or thrice as costly as the latter; at the present day Aleppo scammony has quite lost its pre-eminence.

Localities producing the drug—Scammony is collected in Asia Minor, from Brussa and Boli in the north, to Macri and Adalia in the south, and eastward as far as Angora. But the most productive localities within this area are the valley of the Mendereh, south of Smyrna: and the districts of Kirkagach and Demirjik, north of that town. The neighbourhood of Aleppo likewise affords the drug. A little is obtained further south in Syria, from the woody hills and valleys about the lake of Tiberias and Mount Carmel.

Production—The scammony plant has a long woody root, which throws off downwards a few lateral branches, and produces from its knotty summit numerous twining stems which are persistent and woody at the base. In plants of three or four years old, the root may be an inch or more in diameter; in older specimens it sometimes acquires a diameter of three or four inches. In length, it is from two to three feet, according to the depth of soil in which it grows. When the root is wounded, there exudes a milky juice which dries up to a golden-brown, transparent, gummy-looking substance:—this is pure scammony.

The method followed in collecting scammony for use appears to be nearly the same in all localities. It has been thus described to us by two eye-witnesses, both long resident in the East. Operations commence by clearing away the bushes among which the plant is commonly found; the soil around the latter is then removed, so as to leave 4 or 5 inches of the root exposed. This is then cut off in a slanting direction at 2 to 4 inches below the crown, and a mussel-shell is stuck into it just beneath the lowest edge, so as to receive the milky-sap which instantly flows out. The shells are usually left till evening, when they are collected, and the cut part of the root scraped with a knife, so as to remove any partially dried drops of juice. These latter are called by the Smyrna peasants, kaimak or cream, the softer contents of the shell being called gala or milk.

Sometimes the scammony is allowed to dry in the shell, and such must be regarded as representing the drug in its utmost perfection. But scammony in shells is not brought into commerce, though a little of it is reserved by the peasants for their own use.

The contents of the shells and the scraped off drops are next emptied into a covered copper pot or a leathern bag, carried home, made homogenous by mixing with a knife, and at once allowed to dry. In this way a form of scammony is obtained closely approaching that dried in the shell. But it is a quality of exceptional goodness. Usually the peasant does not dry off the juice promptly, but allows his daily gatherings to accumulate; and when he has collected a pound or two, he places it in the sunshine to soften, and then kneads it, sometimes with the addition of a little water, into a plastic mass, which he lastly allows to dry. By this long exposure to heat, and retention in a liquid state, the scammony juice undergoes fermentation, acquires a strong cheesy odour and dark colour, and when finally dried, exhibits a more or less porous or bubbly structure, never observable in shell scammony.

Scammony is very extensively adulterated. The adulteration is often performed by the peasants, who mix foreign substances into the drug while it is yet soft; and it is also effected by the dealers, some of whom purchase it of the peasants in a half-dried state. The substances used for sophistication are numerous, the commonest and most easily detected being, according to our experience, carbonate of lime and flour. Woodashes, earth (not always calcareous), gum arabic, and tragacanth are also employed; more rarely, wax, yolk of egg, pounded scammony roots, rosin, or black-lead.

Description—The pure juice of the root, simply dried by exposure to the sun and air, is an amorphous, transparent, brittle substance, of resinous aspect, a yellowish-brown colour, and glossy fracture. Scammony possessing these characters is occasionally met with in the form of flattish irregular masses, about ½ to ¾ of an inch in thickness, very brittle by reason of internal fissures, yet with but few air-cavities. In mass, it is of a chesnut-brown, but in small fragments it is seen to be very pale yellowish-brown and transparent, with the freshly fractured surface vitreous and shining. When powdered it is of a very light buff. Rubbed with the moistened finger it forms a white emulsion. Treated with ether it yields 88 to 90 per cent. of soluble matter, and a nearly colourless residuum. This scammony, as well as the pure juice in the shell, is very liable to become mouldy; but besides this, it throws out, if long kept, a white, mammillated, crystalline efflorescence, the nature of which we have not been able to determine. But if scammony is kept quite dry, neither mouldiness nor efflorescence makes its appearance.

The ordinary fine scammony of commerce, known as Virgin Scammony, is also in large flat pieces or irregular flattened lumps and fragments, which in mass have a dark grey or blackish hue. Viewed in thin fragments, it is seen to be translucent and of a yellowish-brown. It is very easily broken, exhibits a shining fracture, gives an ashy-grey powder, and has a peculiar cheesy odour. Some of the pieces have a porous, bubbly structure, indicative of fermentation; the more solid often show the efflorescence already mentioned. Scammony has not much taste, but leaves an acrid sensation in the throat.

Chemical Composition—Scammony owes its active properties as a medicine to a resin shown (1860) by Spirgatis to be identical with that found in the root of the Mexican Ipomœa orizabensis, known in commerce as Male Jalap: this resin called Jalapin will be described in the next article. The other constituents of pure scammony are not well known. One of them is the substance which, as already stated, makes its appearance as small masses of cauliflower crystals on the surface of pure scammony, when the latter is kept in air not perfectly dry.

Whether the odour observable in commercial scammony is due to a volatile fatty acid developed by fermentation, is a question still to be investigated.

Commerce—The export of scammony from Smyrna amounted in 1871 to 278 cases, valued at £8320; in 1872 to 185 cases, value £6100. According to a report of Consul Skene on the trade of Northern Syria, 737 cases of scammony were exported from the province of Aleppo in 1872,—six-sevenths of the quantity being for England. In 1873 Aleppo exported by way of Alexandretta to England 46,500 kilogrammes of scammony root and 900 kilogrammes of the resin, the latter being valued at 36,000 francs (£1444).

An establishment at Brussa, founded by Della Sudda, of Constantinople, is stated to export since 1870 a very good scammony resin extracted by alcohol.

Uses—Employed as an active cathartic, often in combination with colocynth and calomel.

Adulteration—Scammony is very often imported in an adulterated state, but the adulteration is so clumsily effected, and is so easily discoverable by simple tests, or even by ocular examination, that druggists have but little excuse for accepting a bad article.

We have already named the substances used in the sophistication of scammony: of these, the most frequent are carbonate of lime and farinaceous matter. The first may generally be recognized by examining the fractured surface of the drug with a good lens, when the white particles of the carbonate will be perceived. If the surface is then touched (while still sub lente) with hydrochloric acid, effervescence will prove the presence of a carbonate. Other earthly adulterants can be discovered by incineration, or by examining the residue of the drug after treatment with ether. Starchy substances, the presence of which may be surmised by the scammony being difficult to break, are detectable by the microscope or by solution of iodine, a cold decoction of scammony not being affected by that reagent. Scammony that is ponderous, dull and clayey, not easily broken in the fingers, or which when broken does not exhibit a clean, glossy surface, or which does not afford at least 80 per cent. of matter soluble in ether, should be rejected. That which is made up in the form of hard, dark, circular cakes is widely different from pure scammony.

Scammony may be distinguished from Resin of Scammony by its property of forming an emulsion when wetted. The resin is also more glossy and almost entirely soluble in ether.

Radix Scammoniæ.

The frauds commonly practised on the scammony of commerce have given rise to various schemes for obtaining the drug in a purer form, as well as at a more moderate price.

So far back as 1839, the Edinburgh College prescribed a Resina Scammonii, which was prepared by exhausting scammony with a spirit of wine, distilling off the spirit, and washing the residue with water. Such an extract was manufactured by the late Mr. Maltass of Smyrna, and occasionally shipped to London.

In consequence of a suggestion made by Mr. Clark, manufacturer of liquorice at Sochia near Scala Nuova, south of Smyrna, a patent was taken out (1856) by Prof. A. W. Williamson of London, for preparing this resin directly from the dried root by means of alcohol. The same chemist shortly afterwards devised an improved process, which consists in boiling the roots first with water and then with dilute acid, so as to deprive them of all matters soluble in those menstrua, and afterwards extracting the resin by alcohol.

Resin of Scammony, obtained either from scammony or from the dried root, is ordered in the British Pharmacopœia of 1867, and is manufactured by a few houses. It is a brown, translucent, brittle substance of resinous fracture, entirely soluble in ether, and not forming an emulsion when wetted with water.

Scammony root is occasionally brought into the London market, sometimes in rather large quantity, but it is not generally kept by druggists, nor do we find it quoted in price-currents. Its collection is even opposed in some parts of Turkey by the local authorities.

The root consists of stout, woody, cylindrical pieces, often spirally twisted, 2 to 3 inches in diameter, covered with a rough, furrowed, greyish-brown bark. They are internally pale brown, tough and resinous, with a faint odour and taste resembling jalap. A good sample yielded us 5½ per cent. of resin; Kingzett and Farries (1877) showed the root to be devoid of an alkaloid.

Radix Jalapæ.

Tuber Jalapæ; Jalap, Vera Cruz Jalap; F. Racine de Jalap; G. Jalape.

Botanical Origin—Ipomœa Purga Hayne (Convolvulus Purga Wenderoth, Exogonium Purga Bentham), a tuberous-rooted plant, throwing out herbaceous, twining stems, clothed with cordate-acuminate sharply auricled leaves, and bearing elegant salver-shaped, deep pink flowers. It grows naturally on the eastern declivities of the Mexican Andes, at an elevation above the sea of 5000 to 8000 feet, especially about Chiconquiaco and the adjacent villages, and also around San Salvador on the eastern slope of the Cofre de Perote. In these localities where rain falls almost daily, and where the diurnal temperature varies from 15° to 24° C. (60° to 75° F.), the plant occurs in shady woods, flourishing in a deep rich vegetable soil.

The jalap grows freely in the south of England, if planted in a sheltered border, but its flowers are produced so late in autumn that they rarely expand, and the tubers, which develope in some abundance, are liable to be destroyed in winter unless protected from frost.

The plant has been introduced on the Neilgherry Hills in the south of India; it succeeds there remarkably well, and might be extensively propagated if there were any adequate inducement.

History—The use as a purgative of the tuber of a convolvulaceous plant of Mexico, was made known by the early Spanish voyagers; and so highly was the new drug esteemed that large quantities of it reached Europe during the 16th century.

Monardes, writing in 1565, says the new drug was called Ruybarbo de las Indias or Ruybarbo de Mechoacan, the latter name being given in allusion to the province of Michoacan whence the supplies were derived. Some writers have advanced the opinion that mechoacan root was the modern jalap, but in this we do not concur, for the description given of mechoacan and the place of its production do not apply well to jalap. Both drugs were moreover well known about 1610; they were perfectly distinguished by Colin, an apothecary of Lyons (1619), who mentions jalap (“racine de Ialap”) as then newly brought to France. They were however often confounded, or at least only distinguished by their difference of tint. Thus jalap, which at that period used to be imported cut into transverse slices, was termed, from its darker colour, Black Mechoacan; and on the other hand, the paler mechoacan was in later times known as White Jalap.

Mechoacan root is now known to consist (at least in part) of the large thick tuber of Ipomœa Jalapa Pursh (Batatas Jalapa Choisy), a plant of the Southern United States and Mexico. As a drug it has been long obsolete in Europe, having given place to jalap, which is a more active and efficient purgative.

The botanical source of jalap was not definitely ascertained until about the year 1829, when Dr. Coxe of Philadelphia published a description and coloured figure, taken from living plants sent to him two years previously from Mexico.

Manner of Growth—Though we have cultivated the jalap plant for many years, we have had no opportunity of examining the seedling, but judging from analogy suppose that it has at first a small tap-root which gradually thickens after the manner of a radish. A root of jalap, called by some tuber and by others tubercule, throws out in addition to aerial stems, slender, prostrate, underground shoots which emit roots at intervals. These roots while but an inch or two long become thickened and carrot-shaped, gradually enlarging into napiform tuber-like bodies, which emit a few rootlets from their surface and taper off below in long, slender ramifications. The thickened roots have no trace of leaf-organs; the aerial stems grow from the shoot from which they originated.

Fresh jalap roots (tubers) are externally rough and dark brown, internally white and fleshy.

Collection—Jalap is said to be dug up in Mexico during the whole year. The smaller roots are dried entire; the larger are cut transversely, or are gashed so that they may dry more easily. As drying by sun-heat would be almost impracticable owing to the wetness of the climate, the roots are placed in a net, and suspended over the almost constantly burning hearth of the Indian’s hut, where they gradually dry, and at the same time often contract a smoky smell. Much of the jalap that has of late arrived has been more freely sliced than usual, and has obviously been dried with less difficulty.

According to Schiede, whose account was written in 1829, the Indians of Chiconquiaco were at that period commencing the cultivation of jalap in their gardens.

Description—The jalap of commerce consists of irregular, ovoid roots, varying from the size of an egg to that of a hazel-nut, but occasionally as large as a man’s fist. They are usually pointed at the lower end, deeply wrinkled, contorted and furrowed, and of a dark brown hue, dotted over with numerous little, elongated, lighter coloured scars, running transversely. The large roots are incised lengthwise, or cut into halves or quarters, but the smaller are usually entire. Some of the small roots are spindle-shaped or cylindrical; others can be found which are nearly globular, smooth and pitchy-looking, but these latter are seldom solid. Good jalap is ponderous, tough, hard and often horny, becoming brittle when long kept, and breaking with a resinous non-fibrous fracture; internally it is of a pale dingy brown or dirty white. It has a faint smoky, rather coffee-like odour, and a mawkish taste, followed by acridity.

Microscopic Structure—Seen in transverse section, jalap exhibits no radiate structure, but numerous small concentric rings, which in many pieces are very regularly arranged. They are due to the laticiferous cells, differing from the surrounding parenchyme only by their contents and rather large size. These laticiferous cells traverse the tissue in a vertical direction, constituting vertical bands, as may be observed on a longitudinal section; the single cells are simply placed one on the other, and do not form elongated ducts as in Lactuca or Taraxacum.

The fibro-vascular bundles of jalap are neither numerous nor large; they are accompanied by thin-walled cells, so that firm woody rays do not occur. Parenchymatous cells are abundant, and, on a longitudinal fracture especially, if subsequently moistened, are seen to constitute concentric layers. The laticiferous cells are always found in the outer part of each layer. The suberous coat with which the drug is covered is made up of the usual tabular cells.

The parenchyme of jalap is loaded with starch grains; in the pieces which have been submitted to heat in order to dry them, the starch appears as an amorphous mass, and the drug then exhibits a horny consistence and greyish fracture, instead of being mealy. Crystals of calcium oxalate are frequently met with. The laticiferous cells contain the resin of jalap in a semi-fluid state, even in the dry drug; drops of the resinous emulsion flow out of the cells, if thin slices are moistened by any watery liquid.

Chemical Composition—Jalap owes its medicinal efficacy to a resin, which is extractable by exhausting the drug with spirit of wine, concentrating the alcoholic solution to a small bulk, and pouring it into water. The resin precipitated in this manner is then washed and dried; it is contained in jalap to the extent of 12 to 18 per cent.

From this crude resin, which is the Resina jalapæ of the pharmacopœias, ether or chloroform extracts 5 to 7 (12, Umney) per cent. of a resin which, according to Kayser, partially solidifies when in contact with water in crystalline needles. We can by no means confirm Kayser’s statement. The residue (insoluble in ether) is one of the substances to which the name Jalapin has been applied. W. Mayer, 1852-1855, who designated it Convolvulin, found it to have the composition C₃₁H₅₀O₁₆. When purified, it is colourless; it dissolves easily in ammonia as well as in the fixed alkalis, and is not re-precipitated by acids, having been converted by assumption of water into amorphous Convolvulic Acid, which is readily soluble in water. Both convolvulin and convolvulic acid are resolved by moderate heating with dilute acids, or with emulsin, into crystallizable Convolvulinol, C₂₆H₅₀O₇, and sugar. Convolvulinol in contact with aqueous alkalis is converted into Convolvulinolic Acid, C₂₆H₄₈O₆, which is slightly soluble in water and crystallizable.

When convolvulin or its derivatives is treated with nitric acid, it yields several acids, one of which is the Sebacic Acid,

C₈H₁₆ COOH

COOH,

which is to be obtained by treating castor oil or other fatty substances in the same manner. Sebacic acid forms crystalline scales, soluble in boiling water, melting at 128°. That from jalap was first thought to be a peculiar acid, and therefore termed ipomic or ipomœic acid. Its identification is due to Neison and Bayne (1874).

Convolvulin (dry) melts at 150° C., but a small amount of water renders it fusible below 100° C. It is insoluble in oil of turpentine and in ammonia. It dissolves in dilute nitric acid without becoming coloured or evolving gas. Convolvulin possesses in a high degree the purgative property of jalap, but this is not the case with convolvulinol.

The other constituents of jalap include starch, uncrystallizable sugar, gum, and colouring matter. The sugar, according to Guibourt, exists to the extent of 19 per cent.

Commerce—We have no means of knowing to what extent jalap is produced in Mexico. The imports of the drug into the United Kingdom amounted in 1870 to 169,951 lb. Very considerable quantities have of late (1873) appeared in the London drug-sales.

Uses—Jalap is employed as a brisk cathartic.

Other kinds of Jalap.

Besides true jalap, the roots of certain other Convolvulaceæ of Mexico have been employed in Europe, either in the form of jalapin, or as adulterants of the more costly, legitimate drug. The two following have been extensively imported and have been traced to their botanical source; but there are others, of more occasional occurrence, the origin of which has not been ascertained.

1. Light, Fusiform, or Woody Jalap, Male Jalap, Orizaba Root, Jalap Tops or Stalks, Purgo macho of the Mexicans.

This drug is derived from Ipomœa orizabensis Ledanois, a plant of Orizaba, which is but imperfectly known. It is described as a pubescent climber, having a spindle-shaped root about two feet long of woody and fibrous texture. The drug occurs in irregular rectangular or block-like pieces, evidently portions of a very large root, divided transversely and longitudinally. Sometimes it is more like true jalap, being in entire roots, of smaller size, spindle-shaped, not spherical. It has a somewhat lighter colour than jalap, and much deeper longitudinal wrinkles. The larger pieces often exhibit deep cuts from an axe or knife; transverse slices are of rare occurrence. Although generally less ponderous than jalap, the Orizaba drug is nevertheless of a compact and often horny texture. From jalap it is easily distinguished by its radiated transverse section, and the numerous thick bundles of vessels which project as woody fibres from the fractured surface.

In chemical constitution Orizaba root is closely parallel to jalap. The resin was named by Mayer Jalapin; it is the Jalapin of Gmelin’s Chemistry (xvi. 405), and perhaps the jalapin of English pharmacy.

In the pure state it is a colourless amorphous translucent resin, dissolving perfectly in ether, thus differing from convolvulin the corresponding resin of jalap. We find that it is readily soluble also in acetone, amylic alcohol, benzol and phenol, not in bisulphide of carbon. It has the composition of C₃₄H₅₆O₁₆, so that it is homologous with convolvulin; the decomposition-products of jalapin obtained by similar treatment, namely jalapic acid, jalapinol, and jalapinolic acid, are likewise homologous with the corresponding substances obtained from convolvulin. All these bodies when treated with nitric acid yield ipomœic acid. Jalapin has the same fusing point as convolvulin, and behaves in the same manner with alkalis.

The root afforded us 11·8 per cent. of resin dried at 100° C. When perfectly washed, decolorized and dissolved in two parts of alcohol, this resin turned the plane of polarization of a ray of light 9·8° to the left, in a column of 50 mm. long. Convolvulin under the same conditions turned it only 5·8°. The resin of Orizaba root is held by chemists to be identical with that of scammony, of which it has the drastic action.

2. Tampico Jalap,—Purga de Sierra Gorda of the Mexicans. The plant which affords this drug has been described by one of us (1869) under the name of Ipomœa simulans. It is closely related to I. Purga Hayne, from which by its foliage it cannot be distinguished, but it has a bell-shaped corolla and pendulous flower-buds, which are very different. I. simulans Hanbury grows in Mexico along the mountain range of the Sierra Gorda in the neighbourhood of San Luis de la Paz, from which town and the adjacent villages its roots are carried down to Tampico. It has also been found on the lofty Cordillera near Oaxaca, but whether there collected we know not.

The drug, to which in trade the name Tampico Jalap is commonly applied, has been imported during the last few years in considerable quantities. In appearance it closely approaches true jalap, but the roots are generally smaller, more elongated or finger-like, more shrivelled and corky-looking, wanting in the little transverse scars that are plentifully scattered over the roots of true jalap. Many pieces occur however which it is impossible to distinguish by the eye from true jalap, with which it agrees also in odour and taste.

Tampico jalap yielded to one of us 10 per cent. of purified resin, entirely soluble in ether. Umney obtained 12 to 15 per cent. of resin almost wholly soluble in ether; Evans got 13 per cent., but found only about half of this to be soluble in ether. According to Andouard the resin of Tampico jalap is not deficient in purgative powers.

Semen Kaladanæ.

Semen Pharbitidis; Kaladana.

Botanical Origin—Ipomœa Nil Roth (Pharbitis Nil Choisy, Convolvulus Nil L.), a twining annual plant, with a large blue corolla, much resembling the Major Convolvulus (Pharbitis hispida Choisy) of English gardens, but having three-lobed leaves. It is found throughout the tropical regions of both hemispheres, and is common in India, ascending the mountains to a height of 5000 feet.

History—The seeds of this plant were employed in medicine by the Arabian physicians under the name Habbun-nil; and they have probably been long in use among the natives of Hindustan. In recent times they have been recommended by O’Shaughnessy, Kirkpatrick, Bidie, Waring and many other European practitioners in India as a safe and efficient cathartic.

Description—The shape of the seeds is that which would result if a nearly spherical body were divided perpendicularly around its axis into 6 or 8 almost equal segments, only that the back is less regularly vaulted. The seeds are ¼ of an inch high and nearly as much broad; 100 of them weigh on an average about 6 grammes. There is a smaller variety imported from Calcutta, of which 100 seeds weigh but little over 3 grammes; in every other respect the two sorts are identical. Both are of a dull black, excepting at the umbilicus, which is brown and somewhat hairy. The adjacent parts of the thin shell (testa) crack in various directions, if the seed is kept for a short time in cold water. If it is removed from the upper part of the vaulted back, the radicle becomes visible, surrounded by the undulated folds of the cotyledons, which join perpendicularly, but cannot be easily unfolded by reason of the thin seminal integument. Cut transversely, the cotyledons show the same curled structure. Throughout their tissue, small bright glands in considerable number are observable, even without a lens. The kernel, which is devoid of albumen, has at first a nutty taste, with subsequently a disagreeable persistent acridity. When bruised in a mortar, the seeds evolve a heavy earthy smell.

Microscopic Structure—The seed is covered with a dark blackish cuticle, formed of a densely packed tissue, the cells of which show zigzag outlines. The dark brown epidermis is composed of very close cylindrical cells, about 70 mkm. in length and 5 to 7 mkm. in diameter; they require to be treated with chromic acid in order that their structure may be distinctly seen.

The tissue of the kernels is made up of thick-walled cells. Between this tissue and the shell there is a colourless layer, about 70 mkm. thick, of thin-walled corky parenchyme. The cotyledons contain in their narrow tissue numerous granules of albuminous matter, mucilage, a little tannic acid, crystals of oxalate of calcium, and a few starch granules. The glands or hollows, before alluded to as occurring throughout the tissue of the cotyledons, are about 70 mkm. in diameter, and contain an oily liquid.

Chemical Composition—By exhausting the seeds dried at 100° C. with boiling ether, we obtained a thick light brownish oil having an acrid taste and concreting below 18° C. The powdered seeds yielded of this oil 14·4 per cent. Water removes from the seeds a considerable amount of mucilage, some albuminous matter and a little tannic acid. The first is soluble to some extent in dilute spirit of wine, and may be precipitated therefrom by an alcoholic solution of acetate of lead.

The active principle of kaladana is a resin, soluble in alcohol, but neither in benzol nor in ether. From the residue of the seeds after exhaustion by ether, treatment with absolute alcohol removed a pale yellowish resin in quantity equivalent to 8·2 per cent. of the seed.

Kaladana resin, which has been introduced into medical practice in India under the name of Pharbitisin, has a nauseous acrid taste and an unpleasant odour, especially when heated. It melts about 160° C. The following liquids dissolve it more or less freely, namely, spirit of wine, absolute alcohol, acetic acid, glacial acetic acid, acetone, acetic ether, methylic and amylic alcohol, and alkaline solutions. It is on the other hand insoluble in ether, benzol, chloroform, and sulphide of carbon. With concentrated sulphuric acid, it forms a brownish yellow solution, quickly assuming a violet hue. This reaction however requires a very small quantity of the powdered resin. If a solution of the resin in ammonia, after having been kept a short time, is acidulated, no precipitate is formed; but the solution is now capable of separating protoxide of copper from an alkaline solution of the tartrate, which originally it did not alter. Heated with nitric acid, the resin affords sebacic acid (see p. 446).

From these reactions of kaladana resin, we are entitled to infer that it agrees with the resin of jalap or Convolvulin. To prepare it in quantity, it would probably be best to treat the seeds with common acetic acid, and to precipitate it by neutralizing the solution. We have ascertained that the resin is not decomposed when digested with glacial acetic acid at 100° C., even for a week.

We have had the opportunity of examining a sample of kaladana resin manufactured by Messrs. Rogers and Co., chemists of Bombay and Poona, which we found to agree with that prepared by ourselves. It is a light yellowish friable mass, resembling purified jalap resin, and like it, capable of being perfectly decolorized by treatment with animal charcoal.

Uses—Kaladana seeds have cathartic powers like jalap. Besides the resin, an extract, tincture and compound powder have been introduced into the Pharmacopœia of India. In many parts of India the natives take the roasted seeds as a purgative.

Solanaceæ.

Stipes Dulcamaræ.

Caules Dulcamaræ; Bitter-sweet, Dulcamara, Woody Nightshade; F. Douce-amère, Morelle grimpante; G. Bittersüss.

Botanical Origin—Solanum Dulcamara L., a perennial shrubby plant, having small purple flowers and red berries, occurring throughout Europe, except in the extreme north. It is also found in Northern Africa, and in Asia Minor, and has become naturalized in North America. It is common in moist, shady hedges and thickets.

History—Bitter nightshade, “manyglog,” was an ingredient, together with wild sage and betony, of a drink which the Welsh “Physicians of Myddfai” in the 13th century prepared for the bite of a mad dog. The stalks of bitter-sweet were also used in the medical practice by the German physicians and botanists of the 16th century, one of whom, Tragus (1552), has figured and described it, under the name of Dulcis amara or Dulcamarum.

Description—The older stems are woody; the upper and younger are soft and green, long and straggling, attaining by the support of other plants a height of 6 feet or more, and dying back in the winter. For medicinal use, the shoots of a year or two old should be gathered, either late in the year, or early in the spring before the leaves come out. These shoots are several feet long, by about ⅕ of an inch thick, of a light greenish-brown, sometimes cylindrical, at others indistinctly 4-or 5-sided, slightly furrowed longitudinally, or somewhat warty.

The thin, shining cork-bark easily exfoliates, showing beneath it the mesophlœum which is rich in chlorophyll. The stalks are mostly hollow, and partially filled with a whitish pith. The wood when dried is about half or one-third as broad as the hollow centre, and the green bark considerably narrower than the wood; the latter has a radiate structure, and in older stems exhibits two or three sharply-defined annual rings. The stems are usually cut into short lengths before being dried for use.

The odour, which is rather fœtid and unpleasant, is to a great extent dissipated by drying. The taste, at first slightly bitter, is afterwards sweetish. The bitter appears to be more predominant in the spring than in the autumn.

Microscopic Structure—The epidermis of younger shoots consists of tabular thick-walled cells, many of them being elevated from the surface as short blunt hairs. The older stems are covered with the usual suberous envelope. The boundary between the mesophlœum and the endophlœum is marked by a ring of strong liber-fibres, some of which also occur in the pith. The woody part is rich in large vessels. In the parenchymatous tissue of bitter-sweet, small crystals of oxalate of calcium, not of a well-defined outline, and minute starch granules are deposited.

Chemical Composition—The taste of bitter-sweet appears due, according to Schoonbroodt (1867), to a bitter principle yielding by decomposition, sugar and Solanine,—the latter in very small amount. Solanine is an alkaloid; it was first prepared in 1820 by Desfosses, a pharmacien at Besançon, from the berries of Solanum nigrum L., and was subsequently detected by the same chemist in the leaves and stalks of S. Dulcamara, and by Peschier in the berries. Winckler (1841) observed that the alkaloid of dulcamara stems can be obtained only in an amorphous state, and that it behaves to platinic and mercuric chlorides differently from the solanine of potatoes. Moitessier (1856) confirmed this observation, and obtained only amorphous salts of the solanine of bitter-sweet.

Zwenger and Kind on the one hand, and O. Gmelin on the other (1859 and 1858), found that solanine, C₄₃H₆₉NO₁₆ (or C₄₂H₈₇NO₁₅, according to Hilger, 1879), is a conjugated compound of sugar and a peculiar crystallizable alkaloid, Solanidine, C₂₆H₃₉NO (or C₂₆H₄₁NO₂?). The latter, under the influence of strong hydrochloric acid, gives up water, and is converted into the amorphous and likewise basic compound, Solanicine.

Wittstein (1852) stated another alkaloid, dulcamarine, to be present in the stems of bitter-sweet. But Geissler (1875) proved that this substance, when perfectly pure, contains no nitrogen, and is not an alkaloid. Geissler obtained his Dulcamarin by warming an aqueous decoction of the drug with charcoal, which he dried and exhausted with boiling alcohol. This on evaporation afforded a yellowish amorphous matter, which was dissolved in water and mixed with a very little ammonia; a substance containing nitrogen then separated. The liquid was evaporated, the residue again dissolved in alcohol, and the alcohol distilled. Dulcamarin thus obtained is a yellowish powder of at first bitter and subsequently permanently sweet taste. It dissolves in water or alcohol, not in ether, chloroform, bisulphide of carbon. By boiling dulcamarin with dilute acids it splits up according to the following equation:—

C₂₂H₃₄O₁₀ + 2 OH₂ = C₆H₁₂O₆ · C₁₆H₂₆O₆.

Dulcamarin. Sugar. Dulcamaretin.

Dulcamaretin, a dark brown, tasteless mass, is soluble in alcohol, not in water or ether.

Uses—Dulcamara is occasionally given in the form of decoction, in rheumatic or cutaneous affections; but its real action, according to Garrod, is unknown. This physician remarks that it does not dilate the pupil or produce dryness of the throat like belladonna, henbane or stramonium. He has given to a patient 3 pints of the decoction per diem without any marked action, and has also administered as much as half a pound of the fresh berries with no ill effect.

Fructus Capsici.

Pod Pepper, Red Pepper, Guinea Pepper, Chillies, Capsicum; F. Piment ou Corail des Jardins, Poivre d’Inde ou de Guinée; G. Spanischer Pfeffer.

Botanical Origin—The plants, the fruits of which are known as Pod Pepper, have for a long period been cultivated in tropical countries, and are now found in such numerous varieties that an exact determination of the original species is a point of great difficulty. Of several species having pungent fruits, the two following are those which supply the spice found in British commerce:—

1. Capsicum fastigiatum Blume, a small ramous shrub, with 4-sided, fastigiate, diverging branches; fruit-bearing peduncles sub-geminate, slender, erect; fruit very small, subcylindrical, oblong, straight, with calyx obconical and truncate. It occurs apparently wild in Southern India, and is extensively cultivated in Tropical Africa and America.

Roxburgh, who describes this plant under the name C. minimum, terms it East Indian Bird Chilly or Cayenne Pepper Capsicum. Wight says that it is consumed by the natives of India, but that it is not the sort preferred. It is this species that the authors of the British Pharmacopœia have cited as the source of the Fructus Capsici to be used in medicine, and it certainly furnishes the greater part of the Pod Pepper now found in the London market.

2. C. annuum L., an herbaceous (sometimes shrubby?) plant, with fruit extremely variable in size, form, and colour, in some varieties erect, in others pendulous. According to Naudin, in whose opinion we concur, C. longum DC. and C. grossum Willd. are not specifically distinct from this plant. It furnishes the larger kinds of Pod Pepper and, as we believe, much of the Cayenne Pepper which is imported in the state of powder.

History—All species of Capsicum appear to be of American origin; no ancient Sanskrit or Chinese name for the genus is known, and the Latin and Greek names that have been referred to it are extremely doubtful.

The earliest reference to the fruit as a condiment that we have met with, occurs in a letter written in 1494 to the Chapter of Seville by Chanca, physician to the fleet of Columbus in his second voyage to the West Indies. The writer in noticing the productions of Hispaniola, remarks that the natives live on a root called Age, which they season with a spice they term Agi, also eaten with fish and meat. The first of these words signifies yam, the second is the designation of Red Pepper, and still the common name for it in Spanish. Capsicum and its uses are more particularly described by Fernandez, who reached Tropical America from Spain in a.d. 1514.

In the Historia Stirpium of Leonhard Fuchs, published at Basle in 1542, fol. 733, may be found the first and excellent figures of Capsicum longum DC. under the name of Siliquastrum or Calicut Pepper; the author states that the plant has been introduced into Germany from India a few years previously. From this might be inferred an Indian origin; but on the other hand, Clusius asserts that the plant was brought from Pernambuco by the Portuguese, whose commercial intercourse with India would easily explain it being carried thither at an early period. He further states, that the American capsicum had been generally introduced into the gardens at Castille, and that it was used all the year round, green or dried, as a condiment and as pepper. He also saw it cultivated in abundance at Brünn in Moravia in 1585.

Capsicum longum DC. was grown in England by Gerarde (1597 et antea), who speaks of the pods as well known, and sold “in the shops at Billingsgate by the name of Ginnie Pepper.”

Description—As already indicated, the Pod Pepper of commerce is of two kinds, namely:—

1. Fruits of Capsicum fastigiatum—These are ½ to ¾ of an inch in length, by about ²/₁₀ of an inch in diameter, of an elongated, subconical form, tapering to a blunt point, and slightly contracted towards the base. The calyx, which is not always present, is cup-shaped, 5-toothed, 5-sided, supported on a slender, straight pedicel, ¾ to 1 inch long. The fruits, which are somewhat compressed and shrivelled by drying, and also brittle when old, have a leathery, smooth, shining translucent, thin, dry pericarp, of a dull orange-red, enclosing about 18 seeds, attached in two cells to a thin central partition. The seeds have the form of roundish or ovate discs, about ⅛ of an inch in diameter, somewhat thickened at the edges; the embryo is curved, almost into a ring. The taste of the pericarp, and likewise of the seeds, is extremely pungent and fiery. The dried fruit has an odour by no means feeble, which we cannot compare to that of any other substance.

2. Fruits of Capsicum annuum of the commonest variety resemble those of C. fastigiatum, except that they are of longer size, being from 2 to 3 or more inches in length, often rather more tapering towards the extremity. The seeds scarcely surpass in size those of C. fastigiatum.

Microscopic Structure—The pericarp consists of two layers, the outer being composed of yellow thick-walled cells. The inner layer is twice as broad and exhibits a soft shrunken parenchyme, traversed by thin fibro-vascular bundles. The cells of the outer layer especially are the seat of the fine granular colouring matter. If it is removed by an alcoholic solution of potash, a cell-nucleus and drops of fat oil make their appearance. The structural details of this fruit afford interesting subjects for microscopical investigation.

Chemical Composition—Bucholz in 1816, and about the same time Braconnot, traced the acridity of capsicum to a substance called Capsicin. It is obtained by treating the alcoholic extract of ether, and is a thick yellowish-red liquid, but slightly soluble in water. When gently heated, it becomes very fluid, and at a higher temperature is dissipated in fumes which are extremely irritating to respiration. It is evidently a mixed substance, consisting of resinous and fatty matters.

Felletár in 1869 exhausted capsicum fruits with dilute sulphuric acid, and distilled the decoction with potash. The distillate, which was strongly alkaline and smelt like conine, was saturated with sulphuric acid, evaporated to dryness, and exhausted with absolute alcohol. The solution, after evaporation of the alcohol, was treated with potash, and yielded by distillation a volatile alkaloid having the odour of conine.

From experiments made by one of us (F.) we can fully confirm the observations of Felletár. We have obtained the volatile base in question, and find it to have the smell of conine. It occurs both in the pericarp and in the seeds, but in so small proportion that we were unsuccessful in isolating it in sufficient quantity to allow of accurate examination.

Dragendorff states (1871) that petroleum ether is the best solvent for the alkaloid of capsicum; he obtained crystals of its hydrochlorate, the aqueous solution of which was precipitated by most of the usual tests, but not by tannic acid.

The colouring matter of capsicum fruits is sparingly soluble in alcohol, but readily in chloroform. After evaporation, an intensely red soft mass is obtained, which is not much altered by potash; it turns first blue, then black with concentrated sulphuric acid, like many other yellow colouring substances. By alcohol chiefly palmitic acid is extracted from the fruit, as shown by Thresh in 1877.

The fruits of Capsicum fastigiatum have a somewhat strong odour; on distilling consecutively two quantities, each of 50 lb., we obtained a scanty amount of flocculent fatty matter, which possesses an odour suggestive of parsley. Both this matter, as well as the distilled water, were neutral to litmus paper, and the water tasteless. We separated the latter, and exposed the remaining greasy mass to a temperature of about 50° C., when it for the most part melted. The clear liquid on cooling solidified, and now consisted of tufted crystals, which we further purified by recrystallization from alcohol. Thus about 2 centigrammes were obtained of a neutral white stearoptene, having a decidedly aromatic, not very persistent taste, by no means acrid, but rather like that of the essential oil of parsley. The crystals melted at 38° C. On keeping them for some days at the temperature of the water-bath, covered with a watch-glass, some drops of essential oil were volatilized, which had the same taste and did not solidify; the crystals were consequently accompanied by a liquid oil. When kept for some days more in that condition, the crystals themselves began to be volatilized, and the part remaining behind acquired a brownish hue. This no doubt points out another impurity, as we ascertained by the following experiment. With boiling solution of potash, the stearoptene produces a kind of soap, which on cooling yields a transparent jelly. If this is dissolved and diluted, it becomes turbid by addition of an acid. This probably depends upon the presence of a little fatty matter, a suggestion which is confirmed by the somewhat offensive smell given off by our stearoptene if it is heated in a glass tube.

Buchheim’s “Capsicol” is in our opinion a doubtful substance.

Thresh (1876-1877) succeeded in isolating a well defined, highly active principle, the Capsaicin, from the extract which he obtained by exhausting Cayenne pepper with petroleum. From the red liquor dilute caustic lye removes capsaicin, which is to be precipitated in minute crystals by passing carbonic acid through the alkaline solution. They may be purified by recrystallizing them from either alcohol, ether, benzine, glacial acetic acid, or hot bisulphide of carbon; in petroleum capsaicin is but very sparingly soluble, yet dissolves abundantly on addition of fatty oil. The latter being present in the pericarp is the cause why capsaicin can be extracted by the above process.

The crystals of capsaicin are colourless and answer to the formula C₉H₁₄O₂; they melt at 59° C. and begin to volatilize at 115° C., but decomposition can only be avoided by great care. The vapours of capsaicin are of the most dreadful acridity, and even the ordinary manipulation of that substance requires much precaution. Capsaicin is not a glucoside; it is a powerful rubefacient, and taken internally produces very violent burning in the stomach.

Commerce—Chillies or Pod Pepper are shipped from Zanzibar, Western Africa and Natal, but no general statistics of the quantity imported into Great Britain are accessible.

The exports from Sierra Leone in 1871 reached 7258 lb. The colony of Natal, which produces Cayenne Pepper in the county of Victoria, where sugar cane and coffee are also grown, shipped in the same year 9072 lb.

Official returns show that in 1871 Singapore imported 1071 cwt. (119,952 lb.) of chillies, chiefly from Penang and Pegu. The spice is largely consumed by the Chinese.

Bombay imported of dried chillies in the year 1872-3, 5567 cwt. (623,504 lb.) principally from the Madras Presidency, and exported 3323 cwt.

Uses—Capsicum on account of its pungent properties is often administered as a local stimulant in the form of gargle, and occasionally as a liniment; and internally to promote digestion. In all warm countries it is much employed as a condiment.

Radix Belladonnæ.

Belladonna Root; F. Racine de Belladone; G. Belladonnawurzel.

Botanical Origin—Atropa Belladonna L., a tall, glabrous or slightly downy herb, with a perennial stock, native of central and Southern Europe, where it grows in the clearings of woods. The plant extends eastward to the Crimea, Caucasia and Northern Asia Minor. In Britain it is chiefly found in the southern counties, but even of these it is a doubtful native.

In a few localities in England and France, as well as in North America, the plant is cultivated for medicinal use.

History—Although a plant so striking as belladonna can hardly have been unknown to the classical authors, it cannot with certainty be identified in their writings.

Saladinus of Ascoli, who wrote an enumeration of medicinal plants about a.d. 1450, names the leaves of both Solatrum furiale and Solatrum minus, the former of which is probably Belladonna. However this may be, the first indubitable notice of it that we have met with, is in the Grand Herbier printed at Paris, probably about 1504. The plant is also mentioned about this period as Solatrum mortale or Dolwurtz, in the writings of Hieronymus Brunschwyg.

In 1542 belladonna was well figured as Solanum somniferum or Dollkraut by the German botanist Leonhard Fuchs, who fully recognized its poisonous properties. Yet it was confounded by other writers of this period as Tragus, who reproduced Fuchs’ figure as “Solanum hortense!” Strygium and Strychnon were other names not unfrequently applied to Atropa during the 16th and 17th centuries.

Matthiolus, who terms the plant Solatrum majus, states that it is commonly called by the Venetians Herba Bella donna, from the circumstance of the Italian ladies using a distilled water of the plant as a cosmetic. Gesner was also familiar with the name Belladonna. The introduction of the root of belladonna into British medicine is of recent date, and is due to Mr. Peter Squire of London, who recommended it as the basis of a useful anodyne liniment, about the year 1860.

Description—Belladonna has a large, fleshy, tapering root, 1 to 2 inches thick, and a foot or more in length, from which diverge stout branches. Externally the fresh roots are of an earthy brown, rough with cracks and transverse ridges. The bark is thick and juicy, and as well as the more fibrous central portion, is internally of a dull creamy white. A transverse section of the main root shows a distinct radiate structure. The root has an earthy smell with but very little taste at first, but a powerfully acrid after-taste is soon developed.

Dried root of Belladonna is sold in rough irregular pieces of a dirty greyish colour, whitish internally, breaking easily with a short fracture, and having an earthy smell not unlike that of liquorice root. The bark being probably the chief seat of the alkaloid, roots not exceeding the thickness of the finger should be preferred. The drug is for the most part imported from Germany, and is often of doubtful quality. English-grown root purchased in a fresh state (the large and old being rejected), then washed, cut into transverse segments and dried by a gentle heat, furnishes a more reliable and satisfactory article.

Microscopic Structure—There is a considerable structural difference between the main root and its branches, the former alone containing a distinct pith. This pith is included in a woody circle, traversed by narrow medullary rays. In the outer part of the woody circle, parenchymatous tissue is more prevalent than vascular bundles. The transverse section of the branches of the root exhibits a central vascular bundle instead of a medullary column. The outer vascular bundles show no regular arrangement; and medullary rays are not clearly obvious in the transverse section.

The woody parts, both of the main root and its branches, contain very large dotted vessels accompanied by a prosenchymatous tissue. The cells of the latter, however, are always thin-walled; the absence of proper so-called ligneous tissue explains the easy fracture of the root. Sometimes the prosenchyme in which the vessels are imbedded assumes a brownish hue and a waxy appearance, and such parts exhibit a very irregular structure.

In the cortical portion of belladonna root, many of the cells of the middle layer, and likewise some of the central parts of the root, are loaded with extremely small octahedric crystals of calcium oxalate. But most of the parenchymatous cells are filled up with small starch granules.

Chemical Composition—In 1833 Mein prepared from the root, and Geiger and Hesse from the herb, the crystallizable alkaloid Atropine. The researches of Lefort (1872) have proved that the roots contain it in very variable proportions, the young being much richer in alkaloid than the old. The maximum proportion obtained was 0·6 per cent.; this was from root of the thickness of the finger. Large old roots, 7 or 8 years of age, afford from 0·25 to 0·31 per cent. They have besides a smaller proportion of bark than young roots, and it is chiefly in the bark that the alkaloid appears to reside. Manufacturers of atropine employ exclusively the root.

Ludwig and Pfeiffer (1861), by decomposing atropine with potassium chromate and sulphuric acid, obtained benzoic acid and propylamine. Other products are formed when atropine is treated with strong hydrochloric acid, baryta water or caustic soda, thus—Atropine, C₁₇H₂₃NO₂ + H₂O = Tropic Acid, C₉H₁₀O₃ + Tropine, C₈H₁₅NO.

Tropic acid, C₆H₅C(OH) CH₃

COOH,

being further boiled with the same agents is converted into atropic acid,

C₆H₅C CH₂

COOH,

which, especially by using hydrochloric acid, is gradually transformed into isotropic acid. Both these acids are isomeric to cinnamic acid, C₉H₈O₂, but otherwise remarkably dissimilar.

Tropine is a strongly alkaline body, readily soluble both in water and alcohol, and furnishing tabular crystals by the evaporation of its solution in ether. Neither tropine nor tropic acid, it is stated by Kraut (1863), is present in the leaves and root of belladonna.

Hübschmann (1858) detected in belladonna root a second but uncrystallizable alkaloid, called Belladonnine; it has a resinous aspect, is distinctly alkaline, and when heated emits, like atropine, a peculiar odour.

The root further contains, according to Richter (1837) and Hübschmann, a fluorescent substance, as well as a red colouring matter called Atrosin. The latter occurs in greatest abundance in the fruit, and would probably repay further investigation.

Uses—Belladonna root is chiefly used for the preparation of atropine, which is employed for dilating the pupil of the eye. A liniment made with belladonna root is used for the relief of neuralgic pains.

Adulteration—We may point out that the roots of Mandragora microcarpa, M. officinarum, and M. vernalis Bertoloni are very nearly allied to the root under notice, both in external appearance and in their structure. They are not likely to be confounded with Belladonna root, their mother plants being indigenous in the South of Europe.

Folia Belladonnæ.

Belladonna Leaves; F. Feuilles de Belladone; G. Tollkraut.

Botanical Origin—Atropa Belladonna L. (p. 455).

History—Belladonna Leaves and the extract prepared from them were introduced into the London Pharmacopœia of 1809. For further particulars regarding the history of belladonna, see the preceding article.

Description—Belladonna or Deadly Nightshade produces thick, smooth herbaceous stems, which attain a height of 4 to 5 feet. They are simple in their lower parts, then usually 3-forked, and afterwards 2-forked, producing in their upper branches an abundance of bright green leaves, arranged in unequal pairs, from the bases of which spring the solitary, pendulous, purplish, bell-shaped flowers, and large shining black berries.

The leaves are 3 to 6 inches long, stalked, broadly ovate, acuminate, attenuated at the base, soft and juicy; those of barren roots are alternate and solitary. The young shoots are clothed with a soft, short pubescence, which on the calyx is somewhat more persistent, assuming the character of viscid, glandular hairs. If bruised, the leaves emit a somewhat offensive, herbaceous odour which is destroyed by drying. When dried, they are thin and friable, of a brownish-green on the upper surface and greyish beneath, with a disagreeable, faintly bitter taste. Of fresh leaves 100 lb. yield 16 lb. of dried (Squire).

Chemical Composition—The important constituent of belladonna leaves is Atropine. Lefort (1872) estimated its amount by exhausting the leaves previously dried at 100° C. by means of dilute alcohol, concentrating the tincture, and throwing down the alkaloid with a solution of iodohydrargyrate of potassium. The precipitate thus obtained was calculated to contain 33·25 per cent. of atropine. Lefort examined leaves from plants both cultivated and growing wild in the environs of Paris, and gathered either before or after flowering. He found cultivation not to affect the percentage of alkaloid,—that the leaves of the young plant were rather less rich than those taken at the period of full inflorescence,—and that the latter (dried) yielded 0·44 to 0·48 per cent. of atropine.

Larger percentages are recorded by Dragendorff; as much as 0·95 per cent. of atropine as obtained from the dried unripe fruits, 0·83 from the dried leaves, 0·21 from the root. The estimation was performed in nearly the same way as that followed by Lefort.

Belladonna herb yields Asparagin, which according to Biltz (1839) crystallizes out of the extract after long keeping. The crystals found in the extract by Attfield (1862) were however chloride and nitrate of potassium. The same chemist obtained by dialysis of the juice of belladonna, nitrate of potassium, and square prisms of a salt of magnesium containing some organic acid; the juice likewise affords ammonia. The dried leaves yielded us 14·5 per cent. of ash consisting mainly of calcareous and alkaline carbonates.

Uses—The fresh leaves are used for making Extractum Belladonnæ, and the dried for preparing a tincture. They should be gathered while the plant is well in flower.

Herba Stramonii.

Stramonium, Thornapple; F. Herbe de Stramoine; G. Stechapfelblätter.

Botanical Origin—Datura Stramonium L., a large, quick-growing, upright annual, with white flowers like a convolvulus, and ovoid spiny fruits. It is now found as a weed of cultivation in almost all the temperate and warmer regions of the globe. In the south of England it is often met with in rich waste ground, chiefly near gardens or habitations.

History—The question of the native country and early distribution of D. Stramonium has been much discussed by botanical writers. Alphonse De Candolle, who has ably reviewed the arguments advanced in favour of the plant being a native respectively of Europe and America or Asia, enounces his opinion thus:—that D. Stramonium L. appears to be indigenous to the Old World, probably the borders of the Caspian Sea or adjacent regions, but certainly not of India; that it is very doubtful if it existed in Europe in the time of the ancient Roman Empire, but that it appears to have spread itself between that period and the discovery of America.

Stramonium was cultivated in London towards the close of the 16th century by Gerarde, who received the seed from Constantinople and freely propagated the plant, of the medicinal value of which he had a high opinion. The use of the herb in more recent times is due to the experiments of Störck.

Description—Stramonium produces a stout, upright, herbaceous green stem, which at a short distance from the ground, throws out spreading forked branches, in the axil of each fork of which arises a solitary white flower, succeeded by an erect, spiny, ovoid capsule. At each furcation and directed outwards is a large leaf. This arrangement of parts is repeated, and as the plant grows vigorously, it often becomes much branched and acquires in the course of the summer a considerable size.

The leaves of stramonium have long petioles, are unequal at the base, oval, acuminate, sinuate-dentate with large irregular pointed teeth or lobes, downy when young, glabrous at maturity. When fresh they are somewhat firm and juicy, emitting when handled a disagreeable fœtid smell. The larger leaves of plants of moderate growth attain a length of 6 to 8 or more inches.

For medicinal purposes, the entire plants are pulled up, the leaves and younger shoots are stripped off, quickly dried, and then broken and cut into short lengths, so as to be conveniently smoked in a pipe, that being the method in which the drug is chiefly consumed in England. The offensive smell of the fresh plant is lost by drying, being replaced by a rather agreeable tea-like odour. The dried herb has a bitterish saline taste.

Chemical Composition—The leaves of stramonium contain, in common with the seeds, the alkaloid Daturine (see p. 461), but in extremely small proportion, not exceeding in fact ²/₁₀ to ³/₁₀ per mille. They are rich in saline and earthy constituents; selected leaves dried at 100° C. yielded us 17·4 per cent. of ash.

Uses—Scarcely employed in any other way than in smoking like tobacco for the relief of asthma.—Col. Grant (1871) found the herb to be smoked in pipes by the Nubians for chest-complaint.

Substitute—Datura Tatula L.—This plant is closely allied to D. Stramonium L., propagating itself on rich cultivated ground with nearly the same facility; but it is not so generally diffused.

De Candolle is of opinion that it is indigenous to the warmer parts of America, whence it was imported into Europe in the 16th century, and naturalized first in Italy, and then in South-Western Europe. By many botanists it has been united to D. Stramonium, but Naudin, who has studied both plants with the greatest attention, especially with reference to their hybrids, is decidedly in favour of considering them distinct. D. Tatula differs from D. Stramonium in having stem, petiole, and nerves of leaves purplish instead of green; and corolla and anthers of a violet colour instead of white,—characters which, it must be admitted, are of very small botanical value.

D. Tatula has been recommended for smoking in cases of asthma, on the ground of its being stronger than D. Stramonium; but we are not aware of any authority as to the comparative strength of the two species.

Semen Stramonii.

Stramonium Seeds; F. Semences de Stramoine; G. Stechapfelsamen.

Botanical Origin—Datura Stramonium L., see preceding article.

Description—The spiny, ovoid capsule of stramonium opens at the summit in four regular valves. It is bilocular, with each cell incompletely divided into two, and contains a large number (about 400) of flattened, kidney-shaped seeds. The seeds are blackish or dark brown, about 2 lines long and ½ a line thick, thinning off towards the hilum which is on the straighter side. The surface of the seed is finely pitted and also marked with a much coarser series of shallow reticulations or rugosities. A section parallel to the faces of the seed exhibits the long, contorted embryo, following the outline of the testa, and bedded in the oily white albumen. The cylindrical form of the embryo is seen in a transverse section of the seed.

The seeds have a bitterish taste, and when bruised a disagreeable odour. When the entire seeds are immersed in dilute alcohol, they afford a tincture displaying a beautiful green fluorescence, turning yellow on addition of ammonia.

Microscopic Structure—The testa is formed of a row of radially extended, thick-walled cells. They are not of a simply cylindrical form, but their walls are sinuously bent in and out in the direction of their length. Viewed in a direction tangential to the surface, the cells appear as if indented one into the other. Towards the surface of the seed the cell-walls are elevated as dark brown tubercles and folds, giving to the seed its reticulated and pitted surface. The albumen and embryo exhibit the usual contents, namely fatty oil and albuminoid substances.

Chemical Composition—The active constituent of stramonium seeds is the highly poisonous alkaloid Daturine, of which they afford only about ⅒ per cent., while the leaves and roots contain it in still smaller proportion. Daturine was discovered in 1833 by Geiger and Hesse, and regarded as identical with atropine by A. von Planta (1850), who found it to have the same composition as that alkaloid. The two bodies exhibit the same relations as to solubility and fusing point (88-90° C.); and they also agree in crystallizing easily. The experiments of Schroff (1852), tending to show that although daturine and atropine act in the same manner, the latter has twice the poisonous energy of the former, raised a further question as to the identity of the two alkaloids. Poehl (1876) also stated solutions of daturine to be levogyrate, those of atropine being devoid of rotatory power. From the observations of Erhard (1866), it would appear that the crystalline form of some of the salts of atropine and daturine is different. In stramonium seeds daturine appears to be combined with malic acid. The seeds yielded to Cloëz (1865) 2·9 per cent. of ash and 25 per cent. of fixed oil.

Uses—Stramonium seeds are prescribed in the form of extract or tincture as a sedative or narcotic.

Semen Et Folia Daturæ Albæ.

Seeds and Leaves of the Indian or White-flowered Datura.

Botanical Origin—Datura alba Nees, a large, spreading annual plant, 2 to 6 feet high, bearing handsome, tubular, white flowers 5 to 6 inches long. The capsules are pendulous, of depressed globular form, rather broader than high, covered with sharp tubercles or thick short spines. They do not open by regular valves as in D. Stramonium, but split in different directions and break up into irregular fragments.

D. alba appears to be scarcely distinct from D. fastuosa L. Both are common in India, and are grown in gardens in the south of Europe.

History—The mediæval Arabian physicians were familiar with Datura alba, which is well described by Ibn Baytar under precisely the same Arabic name (Jouz-masal) that it bears at the present day; they were also fully aware of its poisonous properties.

Garcia de Orta (1563) observed the plant in India, and has narrated that its flowers or seeds are put into food to intoxicate persons it was designed to rob. It was also described by Christoval Acosta, who in his book on Indian drugs mentions two other varieties, one of them with yellow flowers, the seeds of either being very poisonous, and often administered with criminal intent, as well as for the cure of disease. Graham says of the plant that it possesses very strong narcotic properties, and has on several occasions been fatally used by Bombay thieves, who have administered it in order to deprive their victims of the power of resistance.

The seeds and fresh leaves have a place in the Pharmacopœia of India, 1868.

Description—The seeds of D. alba are very different in appearance from those of D. Stramonium, being of a light yellowish-brown, rather larger size, irregular in shape and somewhat shrivelled. Their form has been likened to the human ear; they are in fact obscurely triangular or flattened-pearshaped, the rounded end being thickened into a sinuous, convoluted, triple ridge, while the centre of the seed is somewhat depressed. The hilum runs from the pointed end nearly half-way up the length of the seed. The testa is marked with minute rugosities, but is not so distinctly pitted as in the seed of the D. Stramonium; it is also more developed, exhibiting in section large intercellular spaces to which are due its spongy texture. The seeds of the two species agree in internal structure as well as in taste; but those of D. alba do not give a fluorescent tincture.

The leaves, which are only employed in a fresh state, are 6 to 10 inches in length, with long stalks, ovate, often unequal at the base, acuminate, coarsely dentate with a few spreading teeth. They evolve an offensive odour when handled.

Microscopic Structure—The testa is built up of the same tissues as in D. Stramonium, but the thick-walled cells constituting the spongy part are far larger, and distinctly show numerous secondary deposits, making a fine object for the microscope.

Chemical Composition—Neither the seeds nor the leaves of D. alba have yet been examined chemically, but there can scarcely be any doubt that their very active properties are due to Daturine, for the preparation of which the former would probably be the best source.

Uses—The seeds in the form of tincture or extract have been employed in India as a sedative and narcotic, and the fresh leaves, bruised and made into a poultice with flour, as an anodyne application.

Folia Hyoscyami.

Henbane Leaves; F. Feuilles de Jusquiame; G. Bilsenkraut.

Botanical Origin—Hyoscyamus niger L., a coarse, erect herb, with soft, viscid, hairy foliage of unpleasant odour, pale yellowish flowers elegantly marked with purple veins, and 5-toothed bottle-shaped calyx. It is found throughout Europe from Portugal and Greece to Central Norway and Finland, in Egypt, Asia Minor, the Caucasus, Persia, Siberia and Northern India. As a weed of cultivation it now grows also in North America and Brazil. In Britain it occurs wild, chiefly in waste places near buildings; and is cultivated for medicinal use.

Henbane exists under two varieties, known as annual and biennial, but scarcely presenting any other distinctive character.

Biennial Henbane (Hyoscyamus niger var. α. biennis) is most esteemed for pharmaceutical preparations. It is raised by seed, the plant producing the first year only a rosette of luxuriant stalked leaves, 12 or more inches in length. In the second, it throws up a flower stem of 2 to 3 feet in height, and the whole plant dies as the fruit matures.

Annual Henbane (H. niger var. β. annua, vel agrestis) is a smaller plant, coming to perfection in a single season. It is the usual wild form, but it is also grown by the herbalists.

History—Hyoscyamus, under which name it is probable the nearly allied South European species, H. albus L., was generally intended, was medicinal among the ancients, and particularly commended by Dioscorides.

In Europe, henbane has been employed from remote times. Benedictus Crispus, archbishop of Milan, in a work written shortly before a.d. 681, notices it under the name of Hyoscyamus and Symphoniaca. In the 10th century, its virtues were particularly recorded by Macer Floridus who called it Jusquiamus.

Frequent mention is made of it in the Anglo-Saxon works on medicine of the 11th century, in which it is called Henbell, and sometimes Belene, the latter word perhaps traceable in βιλινουντία, which Dioscorides gives as the Gallic designation of the plant. In the 13th century henbane was also used by the Welsh “Physicians of Myddvai.”

The word Hennibone, with the Latin and French synonyms Jusquiamus and Chenille, occurs in a vocabulary of the 13th century; and Hennebane in a Latin and English vocabulary of the 15th century. In the Arbolayre, a printed French herbal of the 15th century, we find the plant described as Hanibane or Hanebane with the following explanation—“Elle est aultrement appeler cassilago et aultrement simphoniaca. La semence proprement a nom jusquiame ou hanebane, et herbe a nom cassilago....” Both Hyoscyamus and Jusquiamus are from the Greek Ὑοσκύαμος, i.e. Hog-bean.

Though a remedy undeniably potent, henbane in the first half of the last century had fallen into disuse. It was omitted from the London pharmacopœias of 1746 and 1788, and restored only in 1809. Its re-introduction into medicine was chiefly due to the experiments and recommendations of Störck.

During the middle ages the seeds and roots of henbane were also much used.

Description—The stems of henbane, whether of the annual or biennial form, are clothed with soft, viscid, hairy leaves, of which the upper constitute the large, sessile, coarsely toothed bracts of the unilateral flower-spike. The middle leaves are more toothed and subamplexicaul. The lower leaves are stalked, ovate-oblong, coarsely dentate, and of large size. The stems, leaves, and calyces of henbane are thickly beset with long, soft, jointed hairs; the last joint of many of these hairs exudes a viscid substance occasioning the fresh plant to feel clammy to the touch. In the cultivated plant, the hairiness diminishes.

After drying, the broad light-coloured midrib becomes very conspicuous, while the rest of the leaf shrinks much and acquires a greyish green hue. The drug derived from the flowering plant as found in commerce is usually much broken. The fœtid, narcotic odour of the fresh leaves is greatly diminished by drying. The fresh plant has but little taste.

Dried henbane is sold under three forms, which are not however generally distinguished by druggists. These are 1. Annual plant, foliage and green tops. 2. Biennial plant, leaves of the first year. 3. Biennial plant, foliage and green tops. The third form is always regarded as the best, but no attempt has been made to determine with accuracy the relative merits of the three sorts.

Chemical Composition—Hyoscyamine, the most important among the constituents of henbane, was obtained in an impure state by Geiger and Hesse in 1833. Höhn in 1871 first isolated it from the seeds, which are far richer in it than the leaves. The seeds are deprived of the fatty oil (26 per cent.) and treated with spirit of wine containing sulphuric acid, which takes out the hyoscyamine in the form of sulphate. The alcohol is then evaporated and tannic acid added; the precipitate thus obtained is mixed with lime and exhausted with alcohol. The hyoscyamine is again converted into a sulphate, the aqueous solution of which is then precipitated with carbonate of sodium, and the alkaloid dissolved by means of ether. After the evaporation of the ether, hyoscyamine remains as an oily liquid which after some time concretes into wart-like tufted crystals, soluble in benzol, chloroform, ether, as well as in water. Höhn and Reichardt assign to hyoscyamine the formula C₁₅H₂₃O₃. The seeds yield of it only 0·05 per cent.

Hyoscyamine is easily decomposed by caustic alkalis. By boiling with baryta in aqueous solution, it is split into Hyoscine, C₆H₁₃N, and Hyoscinic Acid, C₉H₁₀O₃. The former is a volatile oily liquid of a narcotic odour and alkaline reaction. By keeping it over sulphuric acid it crystallizes and also yields crystallized salts; hyoscine may be closely allied to conine, C₈H₁₅N. Hyoscinic acid, a crystallizable substance having an odour resembling that of empyreumatic benzoic acid. It melts, according to Höhn, at 105°; tropic acid (see p. 457), melting at 118°, agrees so very nearly with hyoscinic acid that further researches will probably prove these acids to be identical.

Another process for extracting hyoscyamine is due (1875) to Thibaut. He removes by bisulphide of carbon the fatty oil from the powdered seeds, and exhausts them with alcohol slightly acidulated by tartaric acid. The alcohol being distilled off, the author precipitates the alkaloid by means of a solution containing 6 per cent. of iodide of potassium and 3 per cent. iodine. By decomposing the precipitate with sulphurous acid, hydroiodic acid and sulphate of hyoscyamine are formed. The latter is dried up at 35° with magnesia and the hyoscyamine extracted by alcohol or chloroform. The crystals melt at 90°. Thibaut found the alkaloid thus prepared from seeds differing from that yielded by the leaves, the latter having a somewhat strong odour.

Attfield has pointed out that extract of henbane is rich in nitrate of potassium and other inorganic salts. In the leaves, the amount of nitrate is, according to Thorey, largest before flowering, and the same observation applies to hyoscyamine.

Uses—Henbane in the form of tincture or extract is administered as a sedative, anodyne or hypnotic. The impropriety of giving it in conjunction with free potash or soda, which render it perfectly inert, has been demonstrated by the experiments of Garrod. Hyoscyamine, like atropine, powerfully dilates the pupil of the eye.

Substitutes—Hyoscyamus albus L., a more slender plant than H. niger L., with stalked leaves and bracts, a native of the Mediterranean region, is sometimes used in the south of Europe as medicinal henbane. H. insanus Stocks, a plant of Beluchistan, is mentioned in the Pharmacopœia of India as of considerable virulence, and sometimes used for smoking.

Folia Tabaci.

Herba Nicotianæ; Tobacco; F. Tabac; G. Tabakblätter.

Botanical Origin—Nicotiana Tabacum L.—The common Tobacco plant is a native of the New World, though not now known in a wild state. Its cultivation is carried on in most temperate and subtropical countries.

History—It is stated by C. Ph. von Martius that the practice of smoking tobacco has been widely diffused from time immemorial among the natives of South America, as well as among the inhabitants of the valley of the Mississippi as far north as the plant can be cultivated.

The Spaniards became acquainted with tobacco when they landed in Cuba in 1492, and on their return introduced it into Europe for the sake of its medicinal properties. The custom of inhaling the smoke of the herb was learnt from the Indians, and by the end of the 16th century had become generally known throughout Spain and Portugal, whence it passed into the rest of Europe, and into Turkey, Egypt, and India, notwithstanding that it was opposed by the severest enactments both of Christian and Mahommedan governments. It is commonly believed that the practice of smoking tobacco was much promoted in England, as well as in the north of Europe generally, by the example of Sir Walter Raleigh and his companions.

Tobacco was introduced into China, probably by way of Japan or Manila, during the 16th or 17th century, but its use was prohibited by the emperors both of the Ming and Tsing dynasties. It is now cultivated in most of the provinces, and is universally employed.

The first tolerably exact description of the tobacco plant is that given by Gonzalo Fernandez de Oviedo y Valdés, governor of St. Domingo, in his Historia general de las Indias, printed at Seville in 1535. In this work, the plant is said to be smoked through a branched tube of the shape of the letter Y, which the natives call Tabaco.

It was not until the middle of the 16th century that growing tobacco was seen in Europe,—first at Lisbon, whence the French ambassador, Jean Nicot, sent seeds to France in 1560 as those of a valuable medicinal plant, which was even then diffused throughout Portugal.

Monardes, writing in 1571, speaks of tobacco as brought to Spain a few years previously, and valued for its beauty and for its medicinal virtues. Of the latter he gives a long account, noticing also the methods of smoking and chewing the herb prevalent among the Indians. He also supplies a small woodcut representing the plant, which he states to have white flowers, red in the centre.

Jacques Gohory, who cultivated the plant in Paris at least as early as 1572, describes its flowers as shaded with red, and enumerates various medicinal preparations made from it.

In the Maison Rustique of Charles Estienne, edition of 1583, the author gives a “Discours sur la Nicotiane ou Petum mascle,” in which he claims for the plant the first place among medicinal herbs, on account of its singular and almost divine virtues.

The cultivation of tobacco in England, except on a very small scale in a physic garden, has been prohibited by law since 1660.

Description—Amongst the various species of Nicotiana cultivated for the manufacturing of smoking tobacco and snuff, N. Tabacum is by far the most frequent, and is almost the only one named in the pharmacopœias as medicinal. Its simple stem, bearing at the summit a panicle of tubular pink flowers, and growing to the height of a man, has oblong, lanceolate simple leaves, with the margin entire. The lower leaves, more broadly lanceolate, and about 2 feet long by 6 inches wide, are shortly stalked. The stem-leaves are semi-amplexicaul, and decurrent at the base. Cultivation sometimes produces cordate-ovate forms of leaf, or a margin more or less uneven, or nearly revolute.

All the herbaceous parts of the plant are clothed with long soft hairs, made up of broad, ribbon-like, striated cells, the points of which exude a glutinous liquid. Small sessile glands are situated here and there on the surface of the leaf. The lateral veins proceed from the thick midrib in straight lines, at angles of 40° to 75°, gently curving upwards only near the edge. In drying, the leaves become brittle and as thin as paper, and always acquire a brown colour. Even by the most careful treatment of a single leaf, it is not possible to preserve the green hue.

The smell of the fresh plant is narcotic; its taste bitter and nauseous. The characteristic odour of dried tobacco is developed during the process of curing.

Chemical Composition—The active principle of tobacco, first isolated in 1828 by Posselt and Reimann, is a volatile, highly poisonous alkaloid termed Nicotine, C₁₀H₁₄N₂. It is easily extracted from tobacco by means of alcohol or water, as a malate, from which the alkaloid can be separated by shaking it with caustic lye and ether. The ether is then expelled by warming the liquid, which finally has to be mixed with slaked lime and distilled in a stream of hydrogen, when the nicotine begins to come over at about 200° C.

Nicotine is a colourless oily liquid, of sp. gr. 1·027 at 15° C., deviating the plane of polarization to the left; it boils at 247° and does not concrete even at -10° C. It has a strongly alkaline reaction, an unpleasant odour, and a burning taste. It quickly assumes a brown colour on exposure to air and light; and appears even to undergo an alteration by repeated distillation in an atmosphere deprived of oxygen. Nicotine dissolves in water, but separates on addition of caustic potash; it occurs in the dried leaves to the extent of about 6 per cent., but is subject to great variation. The seeds of tobacco are stated by Kosutany as grown in Hungary to contain from 0·28 to 0·67 per cent. of the alkaloid.

It has not been met with in tobacco-smoke by Vohl and Eulenberg (1871), though other chemists assert its occurrence. The vapours were found by the former to contain numerous basic substances of the picolinic series, and ceded to caustic potash, hydrocyanic acid, sulphuretted hydrogen, several volatile fatty acids, phenol and creasote. There was further observed in the imperfect combustion of tobacco the formation of laminæ fusible at 94° C., and having a composition C₁₉H₁₈. Oxide of carbon is also largely met with.

Tobacco leaves, whether fresh or dried, yield when distilled with water a turbid distillate in which, as observed by Hermbstädt in 1823, there are formed, after some days, crystals of Nicotianin or Tobacco Camphor. According to J. A. Barral, nicotianin contains 7·12 per cent. of nitrogen (?). By submitting 4 kilogrammes of good tobacco of the previous year to distillation with much water, we obtained nicotianin, floating on the surface of the distillate, in the form of minute acicular crystals, which we found to be devoid of action on polarized light. The crystals have no peculiar taste, at least in the small quantity we tried; they have a tobacco-like smell, perhaps simply due to the water adhering to them. When an attempt was made to separate them by a filter, they entirely disappeared, being probably dissolved by an accompanying trace of essential oil. The clear water showed an alkaline reaction partly due to nicotine; this was proved by adding a solution of tannic acid, which caused a well-marked turbidity. Nicotianine is in our opinion a fatty acid contaminated with a little volatile oil as in the case of Capsicum (see page 454), or Iris (see article Rhizome Iridis).

Among the ordinary constituents of leaves, tobacco contains albumin, resin and gum. In smoking, these substances, as well as the cellulose of the thick midrib, would yield products not agreeable to the consumer. The manufacturer therefore discards the midrib, and endeavours by further preparation to ensure at least the partial destruction of these unwelcome constituents, as well as the formation of certain products of fermentation (ferment-oils), which may perhaps contribute to the aroma of tobacco, especially when saccharine substances, liquorice, or alcohol, are added in the maceration to which tobacco is subjected.

Tobacco leaves are remarkably rich in inorganic constituents, the proportion varying from 16 to 27 per cent. According to Boussingault, they contain when dry about 1 per cent. of phosphoric acid, and from 3 to 5 per cent. of potash, together with 2½ to 4½ per cent. of nitrogen partly in the form of nitrate, so that to enable the tobacco plant to flourish, it must have a rich soil or continual manuring.

The lime, amounting to between a quarter and a half of the entire quantity of ash, is in the leaf combined with organic acids, especially malic, perhaps also citric. The proportion of potash varies greatly, but may amount to about 30 per cent. of the ash.

Commerce—There were imported into the United Kingdom in the year 1872, 45,549,700 lb. of unmanufactured tobacco, rather more than half of which was derived from the United States of America. The total value of the commodity thus imported was £1,563,382; and the duty levied upon the quantity retained for home consumption amounted to £6,694,037. In 1876 the consumption of tobacco had increased to 47,000,000 lb., i.e. 1½ lb. per head of the population.

In the United States 559,049 acres of land being in 1875 under cultivation with tobacco yielded a crop of 367,000,000 lb.

Uses—Tobacco has some reputation in the removal of alvine obstructions, but it is a medicine of great potency and is very rarely used.

Substitutes—Of the other species of Nicotiana cultivated as Tobacco, N. rustica L. is probably the most extensively grown. It is easily distinguished by its greenish yellow flowers, and its stalked ovate leaves. In spite of their coarser texture, the leaves dry more easily than those of N. Tabacum, and with some care may even be made to retain their green colour. N. rustica furnishes East Indian Tobacco, also the kinds known as Latakia and Turkish Tobacco.

N. persica Lindl. yields the tobacco of Shiraz. N. quadrivalvis Pursh, N. multivalvis Lindl. and N. repanda Willd. are also cultivated plants, the last named, a plant of Havana, being used in the manufacture of a much valued kind of cigar.

Scrophulariaceæ.

Folia Digitalis.

Foxglove Leaves; F. Feuilles de Digitale; G. Fingerhutblätter.

Botanical Origin—Digitalis purpurea L., an elegant and stately plant, common throughout the greater part of Europe, but preferring siliceous soils and generally absent from limestone districts. It is found on the edges of woods and thickets, on bushy ground and commons, becoming a mountain plant in the warm parts of Europe. It occurs in the island of Madeira, in Portugal, Central and Southern Spain, Northern Italy, France, Germany, the British Isles and Southern Sweden, and in Norway as far as 63° N. lat.; it is however very unequally distributed, and is altogether wanting in the Swiss Alps and the Jura. As a garden plant it is well known.

History—The Welsh “Physicians of Myddvai” appear to have frequently made use of foxglove for the preparation of external medicines. Fuchs and Tragus figured the plant; the former gave it the name of Digitalis, remarking that up to the time at which he wrote, there was none for the plant in either Greek or Latin. At that period it was regarded as a violent medicine. Parkinson recommended it in 1640 in the “Theatrum botanicum,” and it had a place in the London Pharmacopœia of 1650 and in several subsequent editions. The investigation of its therapeutic powers (1776-9) and its introduction into modern practice are chiefly due to Withering, a well-known English botanist and physician.

The word foxglove is said to be derived from the Anglo-Saxon Foxes-glew, i.e. fox-music, in allusion to an ancient musical instrument consisting of bells hung on an arched support. In the Scandinavian idioms the plant bears likewise the name of foxes bell.

Description—Foxglove is a biennial or perennial, the leaves of which ought to be taken from the plant while in full flower. The lower leaves are ovate with the lamina running down into a long stalk; those of the stem become gradually narrower, passing into ovate-lanceolate with a short broadly-winged stalk, or are sessile. All have the margin crenate, crenate-dentate, or sub-serrate, are more or less softly pubescent or nearly glabrous on the upper side, much paler and densely pubescent on the under, which is marked with a prominent network of veins. The principal veins diverge at a very acute angle from the midrib, which is thick and fleshy. The lower leaves are often a foot or more long, by 5 to 6 inches broad; those of the stem are smaller.

When magnified, the tip of each crenature or serrature of the leaf is seen to be provided with a small, shining, wart-like gland. The hairs of the lower surface are simple, and composed of jointed cells which flatten in drying; those of the upper surface are shorter.

In preparing foxglove for medicinal use, it is the custom of some druggists to remove the whole of the petiole and the thicker part of the midrib, retaining only the thin lamina, which is dried with a gentle heat. The fresh leaf has when bruised an unpleasant herbaceous smell, which in drying becomes agreeable and tea-like. The dried leaf has a very bitter taste.

Chemical Composition—Since the beginning of the present century, numerous attempts have been made to prepare the active principle of foxglove, and the name Digitalin has been successively bestowed on widely different substances.

Among the investigators engaged in these researches, we may point out Walz (1846-1858), Kosmann (1845-46, 1860), Homolle partly with Quévenne (1845-61), Nativelle (1872), and especially Schmiedeberg (1874). The latter has prepared a new, well-defined, crystallizable principle, Digitoxin, from Digitalis. He exhausted with water the leaves previously dried and powdered, and then extracted them repeatedly with dilute alcohol, 50 per cent.; the tincture thus obtained was then mixed with basic acetate of lead as long as it produced a precipitate. The latter being separated, the filtered liquid was concentrated and the deposit now formed, after some days, removed from the aqueous liquid. It was then washed with a dilute solution of carbonate of sodium, by which a yellow matter (chrysophan?) was partly removed. The substance was then dried, and yielded to chloroform a brownish mass, which after the chloroform had been driven off, was purified by benzin. This liquid dissolved the remainder of the yellow or orange matter, and a little fat, leaving crude digitoxin, which is to be purified by recrystallization from warm alcohol, 80 per cent., adding a little charcoal. This purification still yields yellowish crystals, which ought to be washed again with carbonate of sodium, ether or benzin, and then recrystallized from warm absolute alcohol, containing a little chloroform. This process, however, will only afford colourless crystals provided it be so performed as to cause the separation of digitoxin on account of the cooling of the solution, not by the evaporation of the solvent. If the liquid is instead allowed to evaporate it will soon assume a darker coloration. In the way just pointed out, perfectly colourless scales or needle-shaped crystals of pure digitoxin are at length formed, the yield being not more considerable than about one part from 10,000 of dried leaves.

Digitoxin is insoluble in water, to which it does not even impart its intensely bitter taste as displayed in the alcoholic solution. It is likewise insoluble in benzin or bisulphide of carbon, very sparingly soluble in ether, more abundantly so in chloroform, the latter liquid however acting but very slowly on digitoxin. Its best solvent is alcohol, either cold or warm. The composition of digitoxin answers to the formula, C₃₁H₃₃O₇.

Digitoxin warmed with concentrated hydrochloric acid assumes a yellow or greenish hue, the same which is commonly attributed to commercial “digitalin.” Digitoxin is not a saccharogenous matter; in alcoholic solution it is decomposed by dilute acids, and then affords Toxiresin, an uncrystallizable, yellowish substance, which may easily be separated on account of its ready solubility in ether; it appears to be produced also if digitoxin is maintained for some time in the state of fusion at about 240° C. Toxiresin proved to be a very powerful poison, acting energetically on the heart and muscles of frogs. The very specific action of foxglove is due—not exclusively—to digitoxin; it is so highly poisonous that Schmiedeberg thinks it not at all fit for medicinal use, which might rather be confined to other constituents of foxglove, as, for instance, to those obtained from the seeds under the names of digitalin and digitaléin. The latter, however, are of more difficult extraction than digitoxin.

The preparation of digitoxin is similar to that of Nativelle’s crystallized “digitalin;” the former as well as paradigitogenin are largely found in Nativelle’s digitalin.

The Digitalin of Nativelle—The researches on digitalis of this chemist, for which the Orfila prize of 6000 francs was awarded in 1872, have resulted in the extraction of a crystallized preparation possessing active medicinal properties. It may be obtained by the following process:—

The leaves, previously exhausted by water, are extracted by means of alcohol, sp. gr. ·930. The tincture is concentrated until its weight is equal to that of the leaves used, and then diluted by adding thrice its weight of water. A pitch-like deposit is then formed; digitaléin and other substances remaining in solution. The deposit dried on blotting paper is boiled with double its weight of alcohol, sp. gr. ·907; on cooling, crystals are slowly deposited during some days. They should be washed with a little diluted alcohol (·958) and dried: to purify them, they should be first recrystallized from chloroform, and subsequently from boiling alcohol sp. gr. ·828, some charcoal being used at the same time. Digitalin is thus obtained in colourless needle-shaped crystals. It assumes an intense emerald green colour when moistened with hydrochloric acid, and has an extremely bitter taste. On the animal economy, it displays all the peculiar effects of digitalis, the dose of a milligramme taken by an adult person once or twice a day occasioning somewhat alarming symptoms, but smaller doses exhibiting the sedative power of the herb.

Another body occurring in foxglove is the crystallizable sugar called Inosite, which was detected by Marmé in the leaves, as well as in those of dandelion (p. 394). Pectic matters are also present in foxglove leaves.

Uses—Foxglove is a very potent drug, having the effect of reducing the frequency and force of the heart’s action, and hence is given in special cases as a sedative; it is also employed as a diuretic.

Adulteration—The dried leaves of some other plants have occasionally been supplied for those of foxglove. Such are the leaves of Verbascum, which are easily recognized by their thick coat of branched stellate hairs; of Inula Conyza DC. and I. Helenium L., which have the margin almost entire, and in the latter plant the veins diverging nearly at a right angle from the midrib; in both plants the under side of the leaf is less strongly reticulated than in foxglove. But to avoid all chance of mistake, it is desirable that druggists should purchase the fresh flowering plant, which cannot be confounded with any other, and strip and dry the leaves for themselves.

Acanthaceæ.

Herba Andrographidis.

Kariyát or Creyat.

Botanical Origin—Andrographis paniculata Nees ab E. (Justicia Burm.), an annual herb, 1 to 2 feet high, common throughout India, growing under the shade of trees. It is found likewise in Ceylon and Java, and has been introduced into the West Indies. In some districts of India it is cultivated.

History—It is probable that in ancient Hindu medicine this plant was administered indiscriminately with chiretta, which, with several other species of Ophelia, is known in India by nearly the same vernacular names. Ainslie asserts that it was a component of a famous bitter tincture called by the Portuguese of India Droga amara; but on consulting the authority he quotes we find that the bitter employed in that medicine was Calumba. Andrographis is known in Bengal as Mahā-tīta, literally king of bitters, from the Sanskrit tikta, “bitter,” a title of which it has been thought so far deserving that it has been admitted to a place in the Pharmacopœia of India.

Description—The straight, knotty branch stems are obtusely quadrangular, about ¼ of an inch thick at the base, of a dark green colour and longitudinally furrowed. The leaves are opposite, petiolate, lanceolate, entire, the largest ½ an inch or more wide and 3 inches long. Their upper surface is dark green, the under somewhat lighter, and as seen under a lens finely granular. The leaves are very thin, brittle, and, like the stems, entirely glabrous.

In the well-dried specimen before us, for which we are indebted to Dr. G. Bidie of Madras, flowers are wanting and only a few roots are present. The latter are tapering and simple, emitting numerous thin rootlets, greyish externally, woody and whitish within. The plant is inodorous and has a persistent pure bitter taste.

Chemical Composition—The aqueous infusion of the herb exhibits a slight acid reaction, and has an intensely bitter taste, which appears due to an indifferent, non-basic principle, for the usual reagents do not indicate the presence of an alkaloid. Tannic acid on the other hand produces an abundant precipitate, a compound of itself with the bitter principle. The infusion is but little altered by the salts of iron; it contains a considerable quantity of chloride of sodium.

Uses—Employed as a pure bitter tonic like quassia, gentian, or chiretta, with the last of which it is sometimes confounded.

Sesameæ.

Oleum Sesami.

Sesamé Oil, Gingeli, Gingili or Jinjili Oil, Til or Teel Oil, Benné Oil; F. Huile de Sésame; G. Sesamöl.

Botanical Origin—Sesamum indicum DC., an erect, pubescent annual herb, 2 to 4 feet high, indigenous to India, but propagated by cultivation throughout the warmer regions of the globe, and not now found anywhere in the wild state. In Europe, Sesamum is only grown in some districts of Turkey and Greece, and on a small scale in Sicily and in the islands of Malta and Gozo. It does not succeed well even in the South of France.

History—Sesamé is a plant which we find on the authority of the most ancient documents of Egyptian, Hebrew, Sanskrit, Greek, and Roman literature, has been used by mankind for the sake of its oily seeds from the earliest times. The Egyptian name Semsemt already occurring in the Papyrus Ebers, is still existing in the Coptic Semsem, the Arabic Simsim, and the modern Sesamum. The Indian languages have their own terms for it, the Hindustani Til, from the Sanskrit Tila, being one of the best known. Tila already occurs in the Vedic literature. In the days of Pliny the oil was an export from Sind to Europe by way of the Red Sea, precisely as the seeds are at the present day.

During the middle ages the plant, then known as Suseman or Sempsen, was cultivated in Cyprus, Egypt and Sicily; the oil was an article of import from Alexandria to Venice. Joachim Camerarius gave a good figure of the plant in his “Hortus medicus et philosophicus” 1588 (tab. 44). In modern times sesame oil gave way to that of olives, yet at present it is an article which, if not so renowned, is at least of far greater consumption.

Production—The plant comes to perfection within 3 or 4 months; its capsule contains numerous flat seeds, which are about ²/₁₀10 of an inch long by ¹/₂₀ thick, and weigh on an average ¹/₁₆ of a grain. To collect them, the plant when mature is cut down, and stacked in heaps for a few days, after which it is exposed to the sun during the day, but collected again into heaps at night. By this process the capsules gradually ripen and burst, and the seeds fall out.

The plant is found in several varieties affording respectively white, yellowish, reddish, brown or black seeds. The dark seeds may be deprived of a part of their colouring matter by washing, which is sometimes done with a view to obtain a paler oil.

We obtained from yellowish seeds 56 per cent. of oil; on a large scale, the yield varies with the variety of seed employed and the process of pressing, from 45 to 50 per cent.

Description—The best kinds of sesamé oil have a mild agreeable taste, a light yellowish colour, and scarcely any odour; but in these respects the oil is liable to vary with the circumstances already mentioned. The white seeds produced in Sind are reputed to yield the finest oil.

We prepared some oil by means of ether, and found it to have a sp. gr. of 0·919 at 23° C.; it solidified at 5° C., becoming rather turbid at some degrees above this temperature. Yet sesame oil is more fluid at ordinary temperatures than ground-nut oil, and is less prone to change by the influence of the air. It is in fact, when of fine quality, one of the less alterable oils.

Chemical Composition—The oil is a mixture of olein, stearin and other compounds of glycerin with acids of the fatty series. We prepared with it in the usual way a lead plaster, and treated the latter with ether in order to remove the oleate of lead. The solution was then decomposed by sulphuretted hydrogen, evaporated and exposed to hyponitric vapours. By this process we obtained 72·6 per cent. of Elaïdic Acid. The specimen of sesamé oil prepared by ourselves consequently contained 76·0 per cent. of olein, inasmuch as it must be supposed to be present in the form of triolein. In commercial oils the amount of olein is certainly not constant.

As to the solid part of the oil, we succeeded in removing fatty acids, freely melting, after repeated crystallizations, at 67° C., which may consist of stearic acid mixed with one or more of the allied homologous acids, as palmitic and myristic. By precipitating with acetate of magnesium, as proposed by Heintz, we finally isolated acids melting at 52·5 to 53°, 62 to 63°, and 69·2° C., which correspond to myristic, palmitic and stearic acids.

The small proportion of solid matter which separates from the oil on congelation cannot be removed by pressure, for even at many degrees below the freezing point it remains as a soft magma. In this respect sesamé oil differs from that of olive.

Sesamé oil contains an extremely small quantity of a substance, perhaps resinoid, which has not yet been isolated. It may be obtained in solution by repeatedly shaking 5 volumes of the oil with one of glacial acetic acid. If a cold mixture of equal weights of sulphuric and nitric acids is added in like volume, the acetic solution acquires a greenish yellow hue. The same experiment being made with spirit of wine substituted for acetic acid, the mixture assumes a blue colour, quickly changing to greenish yellow. The oil itself being gently shaken with sulphuric and nitric acids, takes a fine green hue, as shown in 1852 by Behrens, who at the same time pointed out that no other oil exhibits this reaction. It takes place even with the bleached and perfectly colourless oil. Sesamé oil added to other oils, if to a larger extent than 10 per cent., may be recognised by this test. The reaction ought to be observed with small quantities, say 1 gramme of the oil and 1 gramme of the acid mixture, previously cooled.

Commerce—The commercial importance of Sesamé may be at once illustrated by the fact that France imported in 1870, 83 millions; in 1871, 57½ millions; and 1872, 50 millions of kilogrammes (984,693 cwt.) of the seed.

The quantity shipped from British India in the year 1871-72 was 565,854 cwt., of which France took no less than 495,414 cwt. The imports of the seed into the United Kingdom in 1870 were to the value of only about £13,000.

Sesamé is extensively produced in Corea and in the Chinese island of Formosa, which in 1869 exported the exceptionally large quantity of 46,000 peculs (1 pecul = 133 lb.). Zanzibar and Mozambique also furnish considerable quantities of sesamé, whilst on the West Coast of Africa the staple oil-seed is Ground-nut (Arachis hypogæa L. p. 186). The chief place for the manufacture of sesamé oil is Marseilles.

Uses—Good sesamé oil might be employed without disadvantage for all the purposes for which olive oil is used. As its congealing point is some degrees below that of olive oil, it is even more fitted for cool climates. Sesamé seeds are largely consumed as food both in India and Tropical Africa. The foliage of the plant abounds in mucilage, and in the United States is sometimes used in the form of poultice.

Labiatæ.

Flores Lavandulæ.

Lavender Flowers; F. Fleurs de Lavande; G. Lavendelblumen.

Botanical Origin—Lavandula vera DC., a shrubby plant growing in the wild state from 1 to 2 feet high, but attaining 3 feet or more under cultivation. It is indigenous to the mountainous regions of the countries bordering the western half of the Mediterranean basin. Thus it occurs in Eastern Spain, Southern France (extending northward to Lyons and Dauphiny), in Upper Italy, Corsica, Calabria and Northern Africa,—on the outside of the olive region. In cultivation it grows very well in the open air throughout the greater part of Germany and as far north as Norway and Livonia; the northern plant would even appear to be more fragrant, according to Schübeler.

History—There has been much learned investigation in order to identify lavender in the writings of the classical authors, but the result has not been satisfactory, and no allusion has been found which unquestionably refers either to L. vera or to L. Spica, whereas L. Stœchas was perfectly familiar to the ancients.

The earliest mention of lavender that we have observed, occurs in the writings of the abbess Hildegard, who lived near Bingen on the Rhine during the 12th century, and who in a chapter De Lavendula alludes to the strong odour and many virtues of the plant. In a poem of the school of Salerno entitled Flos Medicinæ occur the following lines:—

“Salvia, castoreum, lavendula, primula veris,
Nasturtium, athanas hæc sanant paralytica membra.”

In 1387 cushions of satin were made for King Charles VI. of France, to be stuffed with “lavende.” Its use was also popular at an early period in the British isles, for we find “Llafant” or “Llafanllys” mentioned among the remedies of the “Physicians of Myddvai.” And in Walton’s “Description of an inn,” about the year 1680 to 1690, we find the walls stuck round with ballads, where the sheets smelt of lavender....

Lavender was well known to the botanist of the 16th century.

Description—The flowers of Common Lavender are produced in a lax terminal spike, supported on a long naked stalk. They are arranged in 6 to 10 whorls (verticillasters), the lowest being generally far remote from those above it. A whorl consists of two cymes, each having, when fully developed, about three flowers, below which is a rhomboidal acuminate bract, as well as several narrow smaller bracts belonging to the particular flowers. The calyx is tubular, contracted towards the mouth, marked with 13 nerves and 5-toothed, the posterior tooth much larger than the others. The corolla of a violet colour is tubular, two-lipped, the upper lip with two, the lower with three lobes. Both corolla and calyx, as well as the leaves and stalks, are clothed with a dense tomentum of stellate hairs, amongst which minute shining oil-glands can be seen by the aid of a lens.

The flowers emit when rubbed a delightful fragrance, and have a pleasant aromatic taste. The leaves of the plant are oblong linear, or lanceolate, revolute at the margin and very hoary when young.

For pharmaceutical use or as a perfume, lavender flowers are stripped from the stalks and dried by a gentle heat. They are but seldom kept in the shops, being grown almost entirely for the sake of their essential oil.

Production of Essential Oil—Lavender is cultivated in the parishes of Mitcham, Carshalton and Beddington and a few adjoining localities, all in Surrey, to the extent of about 300 acres. It is also grown at Market Deeping in Lincolnshire; also at Hitchin in Hertfordshire, where lavender was apparently cultivated as early as the year 1568.

At the latter place there were in 1871 about 50 acres so cropped.

The plants which are of a small size, and grown in rows in dry open fields, flower in July and August. The flowers are usually cut with the stalks of full length, tied up in mats, and carried to the distillery there to await distillation. This is performed in the same large stills that are used for peppermint. The flowers are commonly distilled with the stalks as gathered, and either fresh, or in a more or less dry state. A few cultivators distill only the flowering heads, thereby obtaining a superior product. Still more rarely, the flowers are stripped from the stalks, and the latter rejected in toto. According to the careful experiments of Bell, the oil made in this last method is of exceedingly fine quality. The produce he obtained in 1846 was 26½ ounces per 100 lb. of flowers, entirely freed from stalks; in 1847, 25½ ounces; and in 1848, 20 ounces: the quantities of flowers used in the respective years were 417, 633, and 923 lb. Oil distilled from the stalks alone was found to have a peculiar rank odour. In the distillation of lavender, it is said that the oil which comes over in the earlier part of the operation is of superior flavour.

We have no accurate data as to the produce of oil obtained in the ordinary way, but it is universally stated to vary extremely with the season. Warren gives it as 10 to 12 lb., and in an exceptional case as much as 24 lb. from the acre of ground under cultivation. At Hitchin, the yield would appear to approximate to the last named quantity. The experiments performed in Bell’s laboratory as detailed above, show that the flowers deprived of stalks afforded on an average exactly 1½ per cent. of essential oil.

Oil of Lavandula vera is distilled in Piedmont, and in the mountainous parts of the South of France, as in the villages about Mont Ventoux near Avignon, and in those some leagues west of Montpellier (St. Guilhen-le-désert, Montarnaud and St. Jean de Fos)—in all cases from the wild plant. This foreign oil is offered in commerce of several qualities, the highest of which commands scarcely one-sixth the price of the oil produced at Mitcham. The cheaper sorts at least are obtained by distilling the entire plant.

Chemical Composition—The only constituent of lavender flowers that has attracted the attention of chemists is the essential oil (Oleum Lavandulæ). It is a pale yellow, mobile liquid, varying in sp. gr. from 0·87 to 0·94 (Zeller), having a very agreeable odour of the flowers and a strong aromatic taste. The oil distilled at Mitcham (1871) we find to rotate the plane of polarization 4·2° to the left, in a column of 50 mm.

Oil of lavender seems to be a mixture in variable proportions of oxygenated oils and stearoptene, the latter being identical, according to Dumas, with common camphor. In some samples it is said to exist to the extent of one-half, and to be sometimes deposited from the oil in cold weather; we have not however been able to ascertain this fact. The oil according to Lallemand (1859) appears also to contain compound ethers.

Commerce—Dried lavender flowers are the object of some trade in the south of Europe. According to the official Tableau général du Commerce de la France, Lavender and Orange Flowers (which are not separated) were exported in 1870 to the extent of 110,958 kilo. (244,741 lb.),—chiefly to the Barbary States, Turkey and America. There are no data to show the amount of oil of lavender imported into England.

Uses—Lavender flowers are not prescribed in modern English medicine. The volatile oil has the stimulant properties common to bodies of the same class and is much used as a perfume.

Other Species of Lavender.

1. Lavandula Spica DC. is a plant having a very close resemblance to L. vera, of which Linnæus considered it a variety, though its distinctness is now admitted. It occurs over much of the area of L. vera, but does not extend so far north, nor is it found in such elevated situations, or beyond the limit of the olive. It is in fact a more southern plant and more susceptible to cold, so that it cannot be cultivated in the open soil in Britain except in sheltered positions. In Languedoc and Provence, it is the common species from the sea-level up to about 2000 feet, where it is met by the more hardy L. vera.

Lavandula Spica is distilled in the south of France, the flowering wild plant in its entire state being used. The essential oil, which is termed in French Essence d’Aspic, is known to English druggists as Oleum Lavandulæ spicæ, Oleum Spicæ, or Oil of Spike. It resembles true oil of lavender, but compared with that distilled in England it has a much less delicate fragrance. This however may depend upon the frequent adulteration, for we find that flowers of the two plants (L. vera and L. Spica) grown side by side in an English garden, are hardly distinguishable in fragrance. Porta already even, in speaking of the oil of lavender flowers, stated: “e spica fragrantior excipitur, ut illud quod ex Gallia provenit....”—Lallemand (1859) isolated from oil of spike a camphor which he believes to be identical with common camphor.

Oil of Spike is used in porcelain painting and in veterinary medicine.

2. Lavandula Stœchas L.—This plant was well known to the ancients; Dioscorides remarks that it gives a name to the Stœchades, the modern isles of Hières near Toulon, where the plant still abounds. It has a wider range than the two species of Lavandula already described, for it is found in the Canaries and in Portugal, and eastward throughout the Mediterranean region to Constantinople and Asia Minor. It may at once be known from the other lavenders by its flower-spike being on a short stalk, and terminating in 2 or 3 conspicuous purple bracts.

The flowers, called Flores Stœchados or Stœchas arabica, were formerly kept in the shops, and had a place in the London Pharmacopœia down to 1746. We are not aware that they are, or ever were distilled for essential oil, though they are stated to be the source of True Oil of Spike.

Herba Menthæ Viridis.

Spearmint.

Botanical Origin—Mentha viridis L. is a fragrant perennial plant, chiefly known in Europe, Asia and North America, as the Common Mint of gardens, and only found apparently wild in countries where it has long been cultivated. It occurs occasionally in Britain under such circumstances.

Mentha viridis is regarded by Bentham as not improbably a variety of M. silvestris L., perpetuated through its ready propagation by suckers. J. G. Baker remarks, that while these two plants are sufficiently distinct as found in England, yet continental forms occur which bridge over their differences.

History—Mint is mentioned in all early mediæval lists of plants, and was certainly cultivated in the convent gardens of the 9th century. Turner, who has been called “the father of English botany,” states in his Herball that the garden mint of his time was also called “Spere Mynte.” We find spearmint also described by Gerarde who terms it Mentha Romana vel Sarracenica, or Common Garden Mint, but his statement that the leaves are white, soft, and hairy does not well apply to the plant as now found in cultivation.

Description—Spearmint has a perennial rootstock which throws out long runners. Its stem 2 to 3 feet high is erect, when luxuriant branched below with short erecto-patent branches, firm, quadrangular, naked or slightly hairy beneath the nodes, often brightly tinged with purple. Leaves sessile or the lower slightly stalked, lanceolate or ovate-lanceolate, rounded or even cordate at the base, dark green and glabrous above, paler and prominently veined with green or purple beneath, rather thickly glandular, but either quite naked or hairy only on the midrib and principal veins, the point narrowed out and acute, the teeth sharp but neither very close nor deep, the lowest leaves measuring about 1 inch across by 3 or 4 inches long. Inflorescence a panicled arrangement of spikes, of which the main one is 3 or 4 inches long by ⅜ inch wide, the lowest whorls sometimes ½ an inch from each other and the lowest bracts leafy. Bracteoles linear-subulate, equalling or exceeding the expanded flowers, smooth or slightly ciliated. Pedicels about ¾ line long, purplish glandular, but never hairy. Calyx also often purplish, the tube campanulato-cylindrical, ⅜ line long, the teeth lanceolate-subulate, equalling the tube, the flower part of which is naked, but the teeth and often the upper part clothed more or less densely with erecto-patent hairs. Corolla reddish-purple, about twice as long as the calyx, naked both within and without. Not smooth.

The plant varies slightly in the shape of its leaves, elongation of spike and hairiness of calyx. The entire plant emits a most fragrant odour when rubbed, and has a pungent aromatic taste.

Production—Spearmint is grown in kitchen gardens, and more largely in market gardens. A few acres are under cultivation with it at Mitcham, chiefly for the sake of the herb, which is sold mostly in a dried state.

The cultivation of spearmint is carried on in the United States in precisely the same manner as that of peppermint, but on a much smaller scale. Mr. H. G. Hotchkiss of Lyons, Wayne County, State of New York, has informed us that his manufacture of the essential oil amounted in 1870 to 1162 lb. The plant he employs appears from the specimen with which he has favoured us, to be identical with the spearmint of English gardens, and is not the Curled Mint (Mentha crispa) of Germany.

Chemical Composition—Spearmint yields an essential oil (Oleum Menthæ viridis) in which reside the medicinal virtues of the plant. Kane, who examined it, gives its sp. gr. as 0·914, and its boiling point as 160° C. The oil yielded him a considerable amount of stearoptene. Gladstone found spearmint oil to contain a hydrocarbon almost identical with oil of turpentine in odour and other physical properties, mixed with an oxidized oil to which is due the peculiar smell of the plant. The latter oil boils at 225° C.; its sp. gr. is 0·951, and it was found to be isomeric with carvol, C₁₀H₁₄O. According to our experiments the oil, distilled from Curled Mint grown in Germany, deviates the plane of polarization 37°·4 to the left when examined in a column of 100 millimetres. We prepared from it the crystallized compound (C₁₀H₁₄0)₂SH₂, and isolated from it the liquid C₁₀H₁₄O, which differs from carvol (see Fructus Carui, page 306) by its levogyrate power.

Uses—Spearmint is used in the form of essential oil and distilled water, precisely in the same manner as peppermint In the United States the oil is also employed by confectioners and the manufacturers of perfumed soap.

Substitutes—Oil of spearmint is now rarely distilled in England, its high cost causing it to be nearly unsaleable. The cheaper foreign oil is offered in price-currents as of two kinds, namely American and German. Of the first we have already spoken: the second, termed in German Krauseminzöl, is the produce of Mentha aquatica L. var. γ crispa Bentham, a plant cultivated in Northern Germany. Its oil seems to agree with the oil of spearmint.

Herba Menthæ Piperitæ.

Peppermint; F. Menthe poivrée; G. Pfefferminze.

Botanical Origin—Mentha piperita Hudson (non Linn.), an erect usually glabrous perennial, much resembling the Common Spearmint of the gardens, but differing from it in having the leaves all stalked, the flowers larger, the upper whorls of flowers somewhat crowded together, and the lower separate. In the opinion of Bentham it is possibly a mere variety of M. hirsuta L., with which it can be connected by numerous intermediate forms.

Peppermint rapidly propagates itself by runners, and is now found in wet places in several parts of England, as well as on the Continent. It is cultivated on the large scale in England, France, Germany, and North America.

History—Mentha piperita was first observed in Hertfordshire by Dr. Eales, and communicated to Ray, who in the second edition of his Synopsis Stirpium Britannicarum, 1696, noticed it under the name of Mentha spicis brevioribus et habitioribus, foliis Menthæ fuscæ, sapore fervido piperis; and in his Historia Plantarum as “Mentha palustris ... Peper-Mint.” Dale, who found the plant in the adjoining county of Essex, states that it is esteemed a specific in renal and vesical calculus; and Ray, in the third edition of his Synopsis, declares it superior to all other mints as a remedy for weakness of the stomach and for diarrhœa. Peppermint was admitted to the London Pharmacopœia in 1721, under the designation of Mentha piperitis sapore.

The cultivation of peppermint at Mitcham in Surrey dates from about 1750, at which period only a few acres of ground were there devoted to medicinal plants. At the end of the last century, above 100 acres were cropped with peppermint. But so late as 1805 there were no stills at Mitcham, and the herb had to be carried to London for the extraction of the oil. Of late years the cultivation has diminished in extent, by reason of the increased value of land and the competition of foreign oil of peppermint.

On the Continent Mentha Piperitis was grown as early as 1771 at Utrecht; Gaubius appears to have been the first to notice “Camphora Europæa Menthæ Piperitidis,” i.e. Menthol (see page 483).

In Germany peppermint became practically known in the latter half of the last century, especially through the recommendation of Knigge.

Description—The rootstock of peppermint is perennial, throwing out runners. The stem is erect, 3 to 4 feet high, when luxuriant somewhat branched below with erecto-patent branches, firm, quadrangular, slightly hairy, often tinged with purple. Leaves all stalked, the stalks of the lower ½ to ¾ of an inch long, naked or nearly so, the leaf lanceolate, narrowed or rather rounded towards the base, the point narrowed out and acute, the lowest 2 to 3 inches long by about ¾ of an inch broad, naked and dull green above, paler and glandular all over, but only slightly hairy upon the veins beneath; the teeth sharp, fine, and erecto-patent. Inflorescence in a loose lanceolate or acutely conical spike, 2 to 3 inches long by about ¾ of an inch broad at the base, the lowest whorls separate, and usually the lowest bracts leaf-like. Bracteoles lanceolate-acuminate, about equalling the expanded flowers, slightly ciliated. Pedicels 1 to 1½ lines long, purplish, glandular but not hairy. Calyx often purplish, the tube about 1 line long and the teeth ½ a line, the tube campanulate-cylindrical, purplish, not hairy, but dotted over with prominent glands; the teeth lanceolate subulate, furnished with short erecto-patent hairs. Corolla reddish-purple about twice as long as the calyx, naked both within and without. Nut smooth (rugose, according to our observation). The odour and taste are strongly aromatic.

In var. 2. vulgaris of Sole, M. piperita β. Smith, the plant is more hairy, with the spikes broader and shorter, or even bluntly capitate. colourless, pale yellow, or greenish liquid, of sp. gr. varying from 0·84 to 0·92. We learn from information kindly supplied by Messrs. Schimmel and Co., Leipzig, that the best peppermint grown in Germany, carefully dried, affords from 1 to 1·25 per cent. of oil. It has a strong and agreeable odour, with a powerful aromatic taste, followed by a sensation of cold when air is drawn into the mouth. We find that the Mitcham oil examined by polarized light in a column 50 mm. long, deviates from 14°·2 to 10°·7 to the left, American oil 4°·3.

Chemical Composition—The constituent for the sake of which peppermint is cultivated is the essential oil, Oleum Menthæ piperitæ, a coloureless, pale yellow or greenish liquid, of sp. gr. varying from 0·84 to 0·92. We learn from information kindly supplied by Messrs. Schimmel and Co., Leipzig, that the best peppermint grown in Germany, carefully dried from 1 to 1·25 per cent of oil. It has a strong and agreeable odour, with a powerful aromatic taste, followed by a sensation of cold when air is drawn into the mouth. We find that the Mitcham oil examined by polarized light in a column 50 mm. long, deviates from 14·2° to 10·7° to the left, American oil 4·2°.

When oil of peppermint is cooled to -4° C., it sometimes deposits colourless hexagonal crystals of Peppermint Camphor, C₁₀H₁₉OH, called also Menthol. We have never observed it, nor are we aware that menthol has been noticed in America, but it is largely afforded by eastern mints, and found in commerce under the name of Chinese or Japanese Oil of Peppermint, either liquid, and easily depositing the camphor, or also forming a crystalline mass impregnated with the liquid oil.

Pure menthol has the exquisite odour and taste of peppermint; it forms hexagonal crystals, melting at 42° C., and boiling at 212° C. By distilling menthol with P₂O₅ it yields menthene, C₁₀H₁₈, a levogyrate liquid, boiling at 163°, the peculiar odour of which reminds of peppermint. The Chinese crystallized oil of peppermint has sometimes a bitterish after-taste and an odour similar to that of spearmint, but by recrystallization it assumes the pure flavour.

The liquid part of the oil of peppermint has not yet been thoroughly investigated; it appears to consist chiefly of the compound C₁₀H₁₈O. Upon the liquid portions depend the remarkable colorations which the oil of peppermint is capable of assuming. If 50 to 70 drops of the crude oil are shaken with one drop of nitric acid, sp. gr. about 1·2, the mixture changes from faintly yellowish to brownish, and, after an hour or two, exhibits a bluish, violet or greenish colour; in reflected light, it appears reddish and not transparent. The colour thus produced lasts a fortnight. We have thus examined the various samples of peppermint oil at our command, and may state that the finest among them assume the most beautiful coloration and fluorescence, which, however, shows very appreciable differences. An inferior oil of American origin was not coloured; and a very old sample of an originally excellent English oil was likewise not coloured by the test. Menthol is not altered when similarly treated. The nitric acid test is not capable of revealing adulterations of peppermint oil, for the coloration takes place with an oil to which a considerable quantity of oil of turpentine has been added.

Remarkable colorations of a different hue are also displayed by the various kinds of oil of peppermint if other chemical agents are mixed with it. Thus green or brownish tints are produced by means of anhydrous chloral; the oil becomes bluish or greenish or rose-coloured if shaken with a concentrated solution of bisulphite of sodium. It is worthy of note that oils of different origin, which cannot be distinguished by means of nitric acid, exhibit totally different colorations if mixed with either of the liquids just named, or with vapour of bromine. This behaviour may be of some use in the examination of commercial sorts of peppermint oil.

As to bisulphite of sodium, it yields a solid compound with certain kinds of peppermint oil, which we have not yet examined.

Production and Commerce—In several parts of Europe, as well as in the United States, peppermint is cultivated on the large scale as a medicinal plant.

In England the culture is carried on in the neighbourhood of Mitcham in Surrey, near Wisebeach in Cambridgeshire, Market Deeping in Lincolnshire, and Hitchin in Hertfordshire.

At Mitcham in 1850 there were about 500 acres under cultivation; in 1864 only about 219 acres. At Market Deeping there were in 1871 about 150 acres cropped with peppermint. The usual produce in oil may be reckoned at 8 to 12 lb. per acre. The fields of peppermint at Mitcham are level, with a rich, friable soil, well manured and naturally retentive of moisture. The ground is kept free from weeds, and in other respects is carefully tilled. The crop is cut in August, and the herb is usually allowed to dry on the ground before it is consigned to the stills. These are of large size, holding 1000 to 2000 gallons, and heated by coal; each still is furnished with a condensing worm of the usual character, which passes out into a small iron cage secured by a padlock, in which stands the oil separator. The distillation is conducted at the lowest possible temperature. The water that comes over with the oil is not distilled with another lot of herb, but is for the most part allowed to run away, a very little only being reserved as a perquisite of the workmen. The produce is very variable, and no facilities exist for estimating it with accuracy. It is however stated that a ton of dried peppermint yields from 2½ to 3½ pounds of oil, which equals 0·11 to 0·15 per cent. But we have been assured by a grower at Mitcham that the yield is as much as 6 pounds from a ton, or 0·26 per cent.

At Mitcham and its neighbourhood two varieties of peppermint are at present recognized, the one being known as White Mint, the other as Black Mint, but the differences between the two are very slight. The Black Mint has purple stems; the White Mint, green stems, and as we have observed, leaves rather more coarsely serrated than those of the Black. The Black Mint is more prolific in essential oil than the White, and hence more generally cultivated; but the oil of the latter is superior in delicacy of odour and commands a higher price. White Mint is said to be principally grown for drying in bundles, or as it is termed “bunching.”

Peppermint is grown on a vastly larger scale in America, the localities where the cultivation is carried on being Southern Michigan, Western New York, and Ohio. In Michigan where the plant was introduced in 1855, there were in 1858 about 2100 acres devoted to its growth, all with the exception of about 100 acres being in the county of St. Joseph, where there are about 100 distilleries. The average produce of this district was estimated in 1858 at 15,000 lb.; but the yield fluctuates enormously, and in the exceptionally fine season of 1855 it was reckoned at 30,000 lb. We must suppose that it is sometimes much larger, for we have been informed by Mr. H. G. Hotchkiss, of Lyons, Wayne County, State of New York, one of the most well-known dealers, in a letter under date Oct. 10, 1871, that the quantity sent out by him in the previous year reached the enormous amount of 57,365 lb. It is further stated by the official statistics of Hamburg for the year 1876 that this port received 25,840 lb. of peppermint oil from the United States and 14,890 lb. from Great Britain.

From the statistics quoted by Stearns it would appear that the produce of oil per acre is somewhat higher in America than in England, but from various causes information on this head cannot be very reliable.

Peppermint is cultivated at Sens in the department of the Yonne in France and in Germany in the environs of Leipzig, where the little town of Cölleda produces annually as much as 40,000 cwts. of the herb.

The annual crop of the world is supposed to yield 90,000 lb. of peppermint oil.

Peppermint oil varies greatly in commercial value, that of Mitcham commanding twice or three times as high a price as the finest American. Even the oil of Mitcham is by no means uniform in quality, certain plots of ground affording a product of superior fragrance. A damp situation or badly drained ground is well known to be unfavourable to the quantity and quality of oil.

The presence of weeds among the peppermint is an important cause of deterioration to the oil, and at Mitcham some growers give a gratuity to their labourers to induce them to be careful in throwing out other plants when cutting the herb for distillation. One grower of peppermint known to us was compelled to abandon the cultivation, owing to the enormous increase of Mentha arvensis L. which could not be separated, and which when distilled with the peppermint ruined the flavour of the latter. In America great detriment is occasioned by the growth of Erigeron canadensis L. Newly cleared ground planted with peppermint is liable to the intrusion of another plant of the order Compositæ, Erechtites hieracifolia Raf., which is also highly injurious to the quality of the oil.

Uses—A watery or spirituous solution of oil of peppermint is a grateful stimulant, and is a frequent adjunct to other medicines. Oil of peppermint is extensively consumed for flavouring and cordials.

Herba Pulegii.

Pennyroyal; F. Menthe pouliot, Pouliot vulgaire; G. Polei.

Botanical Origin—Mentha Pulegium L., a small perennial aromatic plant, common throughout the south of Europe and extending northward to Sweden, Denmark, England and Ireland, eastward to Asia Minor and Persia, and southward to Abyssinia, Algeria, Madeira and Teneriffe. It has been introduced into North and South America. For medicinal use it is cultivated on a small scale.

History—Pennyroyal was in high repute among the ancients. Both Dioscorides and Pliny describe its numerous virtues. In Northern Europe it was also much esteemed, as may be inferred from the frequent reference to it in the Anglo-Saxon and Welsh works on medicine.

Gerarde considered the plant to be “so exceedingly well known to all our English nation” that it needed no description. In his time (circa 1590), it used to be collected on the commons round London, whence it was brought in plenty to the London markets. At the present day pennyroyal has fallen into neglect, and is not named in the British Pharmacopœia of 1867.

Description—The plant has a low, decumbent, branching stem, which in flowering rises to a height of about 6 inches. Its leaves, scarcely an inch in length and often much less, are petiolate, ovate, blunt, crenate at the margin, dotted with oil-glands above and below. The flowers are arranged in a series of dense, globose whorls, extending for a considerable distance up the stem. The whole plant is more or less hairy. It has a strong fragrant odour, less agreeable to most persons than that of peppermint or spearmint. Its taste, well perceived in the distilled water, is highly aromatic.

Chemical Composition—The most important constituent of pennyroyal is the essential oil, known in pharmacy as Oleum Pulegii, to which is due the odour of the plant. It has been examined by Kane, according to whom it has a sp. gr. of 0·927. Its boiling was found to fluctuate between 183° and 188° C. The formula assigned to it by this chemist is C₁₀H₁₆O. We ascertained that it contains no carvol (see page 481.)

Production—Pennyroyal is cultivated at Mitcham and is mostly sold dried; occasionally the herb is distilled for essential oil. The oil found in commerce is however chiefly French or German, and far less costly than that produced in England.

Uses—The distilled water of pennyroyal is carminative and antispasmodic, and is used in the same manner as peppermint water.

Herba Thymi Vulgaris.

Garden Thyme; F. Thym vulgaire; G. Thymiankraut.

Botanical Origin—Thymus vulgaris L., a small, erect, woody shrub reaching 8 to 10 inches in height, gregarious on sterile uncultivated ground in Portugal, Spain, Southern France and Italy, and in the mountainous parts of Greece. On Mont Ventoux near Avignon, it reaches an elevation above the sea of 3700 ft. (Martins). It is commonly cultivated in English kitchens as a sweet herb, and succeeds as an annual even in Iceland.

History—We are not aware that thyme had any reputation in the antiquity, nor do we know at what period it was first introduced in northern countries. Garden thyme was commonly cultivated in England in the 16th century, and was well figured and described by Gerarde. It is even said to have been formerly grown on a large scale for medicinal use in the neighbourhood of Deal and Sandwich in Kent. Camphor of Thyme was noticed by Neumann, apothecary to the Court at Berlin in 1725; it was called Thymol, and carefully examined in 1853 by Lallemand, and recommended instead of phenol (carbolic acid) in 1868 by Bouilhon, apothecary, and Paquet, M. D. of Lille.

Description—The plant produces thin, woody, branching stems, bearing sessile, linear-lanceolate, or ovate-lanceolate leaves. These are about ¼ of an inch long, revolute at the margin, more or less hoary, especially on the under side, and dotted with shining oil-glands. The small purple flowers are borne on round terminal heads, with sometimes a few lower whorls. The entire wild plant has a greyish tint by reason of a short white pubescence, yet as seen in gardens the plant is more luxuriant, greener and far less tomentose. It is extremely fragrant when rubbed, and has a pungent aromatic taste.

Production of Essential Oil—Though cultivated in gardens for culinary use, common thyme is not grown in England on a large scale. Its essential oil (Oleum Thymi), for which alone it is of interest to the druggist, is distilled in the south of France. In the neighbourhood of Nîmes, where we have observed the process, the entire plant is used, and the distillation is carried on at two periods of the year, namely in May and June when the plant is in flower, and again late in the autumn. The oil has a deep, reddish-brown colour, but becomes colourless though rather less fragrant by re-distillation. The two sorts of oil, termed respectively Huile rouge de Thym and Huile blanche de Thym, are found in commerce. The yield is about 1 per cent.

Oil of thyme is frequently termed in English shops Oil of Origanum, which it in no respect resembles, and which was never, so far as we know, found in commerce.

Chemical Composition—The only constituent of the herb that has attracted any attention is the above-named essential oil. This liquid by fractional distillation is resolved into two portions: the first, more volatile and boiling below 180° C., is a mixture of two hydrocarbons, Cymene, C₁₀H₁₄ (see page 333), and Thymene, C₁₀H₁₆, the latter boiling at 165° C.

The second, named Thymol, C₁₀H₁₄O, which may also be extracted from the crude oil by means of caustic lye, has been described in our article Fructus Ajowan, at page 303. Commercial oil of thyme is said to be sometimes fraudulently deprived of thymol by that treatment.

Uses—Oil of thyme is an efficient external stimulant, and is sometimes employed as a liniment. Its chief consumption is in veterinary medicine. Thymol has been proposed as a disinfectant in the place of carbolic acid, in cases in which the odour of the latter is objectionable. The herb is not used in modern English medicine, but is often employed on the Continent.

Herba Rosmarini.

Herba Anthos; Rosemary; F. Romarin; G. Rosmarin.

Botanical Origin—Rosmarinus officinalis L., an evergreen shrub, attaining a height of 4 feet or more, abundant on dry rocky hills of the Mediterranean region, from the Spanish peninsula to Greece and Asia Minor. It generally prefers the neighbourhood of the sea, but occurs even in the Sahara, where it is collected and conveyed by caravans to Central Africa. It does not succeed well in Germany.

History—Rosemary is mentioned by Pliny, who ascribes to it numerous virtues. It was also familiar to the Arab physicians of Spain, one of whom, Ibn Baytar (13th cent.), states it to be an object of trade among the vendors of aromatics. In the middle ages rosemary was doubtless much esteemed, as may be inferred from the fact that it was one of the plants which Charlemagne ordered to be grown on the imperial farms.

It was probably in cultivation in Britain prior to the Norman Conquest, as it is recommended for use in an Anglo-Saxon herbal of the 11th century. In the “Physicians of Myddvai” a curious chapter is devoted to the virtues of Rosemary, called “Ysbwynwydd, and Rosa Marina in Latin.” The essential oil was distilled by Raymundus Lullus about a.d. 1330. John Philip de Lignamine, a writer of the 15th century, describes Rosemary as the usual condiment of salted meats.

Description—Rosemary has sessile, linear, entire, opposite leaves about an inch in length, revolute at the margin; they are of coriaceous texture, green and glabrous above, densely tomentose and white beneath. Examined under a lens, the tomentum both of the leaves and young shoots is seen to consist of white stellate hairs; in that of the shoots which is less dense, minute oil-glands are discernible. These glands are of two kinds, large and small, and probably do not yield one and the same oil. The flowers have a campanulate 2-lipped calyx, and a pale blue and white corolla, the upper lip of which is emarginate and erect, the lower 3-lobed with the central lobe concave and pendulous. The whole plant has a very agreeable smell and a strong aromatic taste. It flowers in the early spring.

Production of Essential Oil—Rosemary is cultivated on a very small scale in English herb-gardens, and though a little oil has been occasionally distilled from it, English oil of rosemary is an article practically unknown in commerce. That with which the market is supplied is produced in the south of France and on the contiguous coasts of Italy. The plant, which is plentifully found wild, is gathered in summer (not while in flower) and distilled, the operator being sometimes an itinerant herbalist who carries his copper alembic from place to place, erecting it where herbs are plentiful, and where a stream of water enables him to cool a condenser of primitive construction.

Oil of rosemary is also produced on a somewhat large scale in the island of Lesina, south of Spalato in Dalmatia, whence it is exported by way of Trieste, even to France and Italy, to the extent of 300 to 350 quintals annually.

Some of the French manufacturers of essences offer oil of rosemary at a superior price as drawn from the flowers, by which we presume is meant the flowering tops, for the separation of the actual flowers would be impracticable on a large scale. The great bulk of the oil found in commerce is however that distilled from the entire plant.

Chemical Composition—The peculiar odour of rosemary depends on the essential oil, which is the only constituent of the plant that has afforded matter for chemical research.

Lallemand (1859) by fractional distillation, resolved oil of rosemary into two liquids,—the one a mobile hydrocarbon boiling at 165° C. and turning the plane of polarization to the left; the other, boiling between 200° and 210° C., deposits when exposed to a low temperature a large quantity of camphor. Gladstone (1864) found the oil to consist almost wholly of a hydrocarbon, C₁₀H₁₆. This, according to our experiments, constitutes about ⁴/₅ of the oil; it deviates the plane of polarization to the left, whereas a fraction boiling at 200° to 210° C. deviates to the right. By warming the latter with nitric acid, we observed the odour of common camphor, and may therefore infer that a compound, C₁₀H₁₈O, is present in the oil under examination.

From Montgolfier’s investigations (1876) it would appear that the stearoptene or camphor above alluded to is a mixture of a dextrogyrate and a lævogyrate substance.

Uses—The flowering tops and dried leaves are kept by the herbalists, but are not used in regular medicine. The volatile oil is employed as an external stimulant in liniments, and also as a perfume. Rosemary is popularly supposed to promote the growth of the hair.

Plantagineæ.

Semen Ispaghulæ.

Ispaghúl Seeds, Spogel Seeds.

Botanical Origin—Plantago decumbens Forsk. (P. Ispaghula Roxb.), a plant of variable aspect, from an inch to a foot in height, erect or decumbent, with linear lanceolate leaves which may be nearly glabrous, or covered with shaggy hairs. The flower-spikes differ according to the luxuriance of the plant, being in some specimens cylindrical and 1½ inches long, in others reduced to a globular head. The plant has a wide range, occurring in the Canary Islands, Egypt, Arabia, Beluchistan, Afghanistan, and North-western India. Stewart says it is common in the Peshawar valley and Trans-Indus generally up to 2000 feet; also on the plains and lower hills of the Punjab, but that he has never seen it cultivated in the latter region. It is said to be cultivated at Multan and Lahore, also in Bengal and Mysore.

History—The seeds which are found in all the bazaars of India and are held in great esteem, are generally designated by the Persian word Ispaghúl; but they also bear the Arabic name Bazre-qatúná, under which we find them mentioned by the Persian physician Alhervi in the 10th century, and about the same period or a little later by Avicenna. Several other Oriental writers are quoted by Ibn Baytar as referring to a drug of the same name, which may possibly have included the seeds of other species, as Plantago Psyllium L. and P. Cynops, having similar properties, and known to have been used from an early period.

J. H. Linck, whom we mentioned in our article on Oleum Cajuputi (p. 278), described in 1719 the seed under notice, yet without knowing its name; it further attracted the notice of Europeans towards the close of the last century, and has been often prescribed as a demulcent in dysentery and diarrhœa. It was admitted to the Pharmacopœia of India of 1868.

Description—The seeds, like those of other species of Plantago, are of boat-shaped form, the albumen being deeply furrowed on one side and vaulted on the other. They are a little over ⅒ of an inch in length and nearly half as broad, and so light that 100 weigh scarcely three grains. Their colour is a light pinkish grey with an elongated brown spot on the vaulted back, due to the embryo, which at this point is in close contact with the translucent testa. From this brown spot the thick radicle runs to the top of the seed. The hollow side of the seed is also brown and partially covered with a thin white membrane.

The seeds are highly mucilaginous in the mouth, but have neither taste nor odour. Those of the allied P. Psyllium have nearly the same form, but are shining and of a dark brown hue.

Microscopic Structure—This can be best investigated by immersing the seed in benzol, as in this medium the mucilage is insoluble. When thus examined, the whole surface is seen to consist of polyhedral cells, separated by a very thin brown layer from the albumen, which on the back of the seed is only 70 mkm. thick. The albumen is made up of thick-walled cells, loaded with granules of matter which acquire an orange hue on addition of iodine. The two cotyledons adhere in a direction perpendicular to the bottom of the furrow; their tissue is composed of thin-walled smaller cells, containing also albuminous granules and drops of fatty oil.

If the seed is immersed in water, the cells composing the epidermis instantly swell and elongate, and soon burst, leaving only fragments of their walls. When examined under glycerin, the change is more gradual, and the outer walls of the cells yielding the mucilage display a series of thin layers, which slowly swell and disappear by the action of water. The mucilage is consequently not contained within the cells, but is formed of the secondary deposits on their walls, as in linseed and quince pips.

Chemical Composition—Mucilage is so abundantly yielded by these seeds, that one part of them with 20 parts of water forms a thick tasteless jelly. On addition of a larger quantity of water and filtering, but little mucilage passes, the greater part of it adhering to the seeds. The mucilage separated by straining with pressure does not redden litmus, is not affected by iodine, nor precipitated by borax, alcohol or ferric chloride. The fat oil and albuminous matter of the seed have not been examined.

Uses—A decoction of the seeds (1 p. to 70 p. of water) is employed in India as a cooling, demulcent drink. The seeds powdered and mixed with sugar, or made gelatinous with water, are sometimes given in chronic diarrhœa.

Polygonaceæ.

Radix Rhei.

Rhubarb; F. Rhubarbe; G. Rhabarber.

Botanical Origin—No competent observer, as far as we know, has ever ascertained as an eye-witness the species of Rheum which affords the commercial rhubarb. Rheum officinale, from which it seems, at least partly, derived is the only species yielding a rootstock which agrees with the drug.

Rheum officinale Baillon is a perennial noble plant resembling the Common Garden Rhubarb, but of larger size. It differs from the latter in several particulars: the leaves spring from a distinct crown rising some inches above the surface of the ground; they have a subcylindrical petiole, which as well as the veins of the under side of the lamina is covered with a pubescence of short erect hairs. The lamina, the outline of which is orbicular, cordate at the base, is shortly 5-to 7-lobed, with the lobes coarsely and irregularly dentate; it attains 4 to 4½ feet in length and rather more in breadth. The first leaves in spring display before expanding the peculiar metallic red hue of copper.

The plant was discovered in South-eastern Tibet, where it is said to be often cultivated for the sake of its medicinal root; but it is supposed to grow in various parts of Western and North-western China, whence the supplies of rhubarb are derived. It was obtained by the French missionaries about the year 1867 for Dabry, French Consul at Hankow, who transmitted specimens to Dr. Soubeiran of Paris. From one of these which flowered at Montmorency in 1871, a botanical description was drawn up by Baillon.

To what extent the rhubarb of commerce is derived from this plant is not known. But that the latter may be a true source of the drug is supported by the fact, that there is at least no important discrepancy between it and the accounts and figures, scanty and imperfect though they are, given by Chinese authors and the old Jesuit missionaries; and still more by the agreement in structure which exists between its root and the Asiatic rhubarb of commerce.

We have engaged in 1873 Mr. Rufus Usher at Bodicott (see below, p. 500) to cultivate Rheum officinale, which is there admirably succeeding; but it must be granted that as yet the root, notwithstanding the most careful preparation in drying it, is far from displaying the rich yellow of the commercial drug. It is most obviously marked on the other hand with the characteristic ring of stellate markings, which we have constantly observed in many roots of Rheum officinale cultivated by us at Clapham Common near London, as well as at Strassburg or, by other observers, at Paris.

Rheum palmatum L., a species known as long as 1750, has always been supposed to yield also rhubarb, and this has again been asserted by the Russian Colonel Przewalski, who observed in 1872 and 1873 that plant in the Alpine parts of Tangut round the Lake Kuku-nor, in the Chinese province of Kansu, in 36°-38° North Lat.—Rheum palmatum has been frequently cultivated in Russian Asia and in many parts of Europe since the last century, but without producing a root agreeing with Chinese rhubarb. Now, Przewalski states that from this species the drug under notice is largely collected along the river Tetung-gol (or Datung-ho), a tributary of the upper Hoang-ho, northward of the Kuku-nor. Specimens of that root were largely brought to St. Petersburg by Przewalski, but Dragendorff expressly points out in his Jahresbericht for 1877 (p. 78) that it is dissimilar to true rhubarb.

History—The Chinese appear to have been acquainted with the properties of rhubarb from a period long anterior to the Christian era, for the drug is treated of in the herbal called Pen-king, which is attributed to the Emperor Shen-nung, the father of Chinese agriculture and medicine, who reigned about 2700 b.c. The drug is named there Huang-liang, yellow, excellent, and Ta-huang, the great yellow. The latter name also occurs in the great Geography of China, where it is stated that rhubarb was a tribute of the province Si-ning-fu, eastward of Lake Kuku-nor, from about the 7th to the 10th centuries of our era.

As regards Western Asia and Europe, we find a root called ῤᾶ or ῤῆον, mentioned by Dioscorides as brought from beyond the Bosphorus. The same drug is alluded to in the fourth century by Ammianus Marcellinus, who states that it takes its name from the river Rha (the modern Volga), on whose banks it grows. Pliny describes a root termed Rhacoma, which when pounded yielded a colour like that of wine but inclining to saffron, and was brought from beyond Pontus.

The drug thus described is usually regarded as rhubarb, or at least as the root of some species of Rheum, but whether produced in the regions of the Euxine (Pontus), or merely received thence from remoter countries, is a question that cannot be solved.

It is however certain that the name Radix pontica or Rha ponticum, used by Scribonius Largus and Celsus, was applied in allusion to the region whence the drug was received. Lassen has shown that trading caravans from Shensi in Northern China arrived at Bokhara as early as the year 114 b.c. Goods thus transported might reach Europe either by way of the Black Sea, or by conveyance down the Indus to the ancient port of Barbarike. Vincent suggests that the rha imported by the first route would naturally be termed rha-ponticum, while that brought by the second might be called rha-barbarum.

We are not prepared to accept this plausible hypothesis. It receives no support from the author of the Periplus of the Erythrean Sea (circa a.d. 64), whose list of the exports of Barbarike does not include rhubarb; nor is rhubarb named among the articles on which duty was levied at the Roman custom-house of Alexandria (a.d. 176-180).

The terms Rheum barbarum vel barbaricum or Reu barbarum occur in the writings of Alexander Trallianus about the middle of the 6th century, and in those of Benedictus Crispus, archbishop of Milan, and Isidore of Seville, who both flourished in the 7th century. Among the Arabian writers on medicine, the younger Mesue, in the early part of the 11th century, mentions the rhubarb of China as superior to the Barbaric or Turkish. Constantinus Africanus about the same period speaks of Indian and Pontic Rheum, the former of which he declares to be preferable. In 1154 the celebrated Arabian geographer Edrisi mentions rhubarb as a product of China, growing in the mountains of Buthink—probably the environs of north-eastern Tibet near Lake Tengri Nor (or Bathang in Western Szechuen?).

Rhubarb in the 12th century was probably imported from India, as we may infer from the tariff of duties levied at the port of Acon in Syria, in which document it is enumerated along with many Indian drugs. A similar list of a.d. 1271, relating to Barcelona, mentions Ruibarbo. In a statute of the city of Pisa called the Breve Fundacariorum, dating 1305, rhubarb (ribarbari) is classified with commodities of the Levant and India.

The first and almost the only European who has visited the rhubarb-yielding countries of China is the famous Venetian traveller, Marco Polo, who speaking of the province of Tangut says—“ ... et par toutes les montagnes de ces provinces se treuve le reobarbe en grant habondance. Et illec l’achatent les marchans et le portent par le monde.”

A sketch of the history of rhubarb would be incomplete without some reference to the various routes by which the drug has been conveyed to Europe from the western provinces of the Chinese Empire, and which have given rise to the familiar designations of Russian, Turkey and China Rhubarb.

The first route is that over the barren steppes of Central Asia by Yarkand, Kashgar, Turkestan, and the Caspian to Russia; the second by the Indus or the Persian Gulf to the Red Sea and Alexandria, or by Persia to Syria and Asia Minor; and the third by way of Canton, the only port of the Chinese Empire which, previous to the year 1842, held direct communication with Europe.

In 1653 China first permitted Russia to trade on her actual frontiers. The traffic in Chinese goods was thereupon diverted from the line of the Caspian and Black Sea further north, taking its way from Tangut across the steppes of the high Gobi, and through Siberia by Tobolsk to Moscow. Thus it is mentioned in 1719 that Urga on the north edge of the Gobi desert was the principal depôt for rhubarb. From the earliest times, Bucharian merchants appear to have been agents on this traffic, the producers of the drug never concerning themselves about its export.

Consequent on the rectification of frontier in 1728, a line of custom-houses was established by treaty between Russia and China, whereby the commerce, previously unrestricted, was limited to the government caravans which passed the frontier only at Kiachta and at Zuruchaitu, south of Nerchinsk. The latter place always remained unimportant, while Kiachta and the opposite Chinese town of Maimatchin became the staple depôts of rhubarb.

The root was subjected to special control as early as 1687-1697 by the Russian Government, who finally monopolized the trade about 1704. Caravans fitted out by the Crown alone brought the drug to Moscow, until 1762, when the caravan-trade was for a while thrown open. It was not until this period that the export of rhubarb became considerable, although the stringent regulations, established in 1736, were still maintained. The surveillance of rhubarb was exercised at Kiachta in a special court or office called the Brake, under instructions from the Russian Minister of War, by an apothecary appointed for six years, the object being to remove from the rhubarb brought for inspection all inferior or spurious pieces, and to improve the selected drug by trimming, paring and boring. It was then carefully dried, and packed in chests, which were sown up in linen, and rendered impervious to wet by being pitched and then covered with hide. The drug was dispatched, but only in quantities of 1000 puds (40,000 lb.), once a year by way of Lake Baikal and Irkutsk to Moscow, whence it was transmitted to St. Petersburg, to be there delivered to the Crown apothecaries and in part to be sold to druggists.

We are indebted for these accounts chiefly to Calau, an apothecary appointed to supervise the examination of rhubarb, and who resided a long time at Kiachta. An exact account of the remarkable policy of the Russian Government in relation to that drug was also given by Von Schröders in 1864.

So long as China kept all her ports closed to foreign commerce except Canton in the extreme south, a large supply of fine rhubarb found its way to Europe by way of Russia. But the unpleasant accompaniments of the Russian supervision, which was exercised with unsparing severity, and the extreme tediousness of the land-transport, made the Chinese very ready to accept an easier outlet for their goods. Accordingly we find that the opening of a number of ports in the north of China exerted a very depressing influence on the trade of Kiachta, which was augmented by the rebellion that raged in the interior of China for some years from 1852.

On these accounts Russia in 1855 removed certain restrictions on the trade, though without abandoning the Rhubarb Office. She withdrew in 1860 the custom-house to Irkutsk, and declared Kiachta a free port, while by the treaty with China of November 1860, she insisted on that country abandoning all restrictions on trade.

But the overland rhubarb trade had already been destroyed: the Chinese, tempted by the increased demand occasioned by the new trading-ports, became less careful in the collection and curing of the root, while the Russians insisted with the greatest strictness on the drug being of the accustomed quality. Hence it happened that from 1860 hardly any rhubarb was delivered at Kiachta, either for the government use or to private traders; and in 1863 the Rhubarb Office was abolished.

Thus the so-called Russian or Muscovitic or Crown Rhubarb, familiarly known in England as Turkey Rhubarb, a drug which for its uniformly good quality long enjoyed the highest reputation, has become a thing of the past, which can only now be found in museum collections. It began to appear in English commerce at the commencement of the last century. Alston, who lectured on botany and materia medica at Edinburgh in 1720, speaks of rhubarb as brought from Turkey and the East Indies,—“and of late, likewise from Muscovy.”

It has been shown (p. 494) that rhubarb was shipped from Syria in the 12th century. Vasco da Gama mentions it in 1497 among the exports of Alexandria. In fact, the drug was carried from the far east to Persia, whence it was brought by caravans to Aleppo, Tripoli, Alexandria, and even to Smyrna. From these Levant ports it reached Europe, and was distributed as Turkey Rhubarb; while that which was shipped direct from China, or by way of India, became known as China, Canton, or East India Rhubarb. The latter was already the more common sort in England as early as 1640.

As the rhubarb of the Levant disappeared from trade, that of Russia took not only its place but likewise its name, until the term “Turkey Rhubarb” came to be the accepted designation of the drug imported from Russia. This strange confusion of terms was not however prevalent on the Continent, but was chiefly limited to British trade.

The risk and expense of the enormous land-transport over almost the whole breadth of Asia, caused rhubarb in ancient times to be one of the very costly drugs. Thus at Alexandria in 1497, it was valued at twelve times the price of benzoin. In France in 1542, it was worth ten times as much as cinnamon, or more than four times the price of saffron. At Ulm in 1596, it was more costly than opium. A German price-list of the magistrate of Schweinfurt, of 1614, shows Radix Rha Barbari to be six times as dear as fine myrrh, and more than twice the price of opium. An official English list giving the price of drugs in 1657, quotes opium as 6s. per lb., scammony 12s., and rhubarb 16s.

Production and Commerce—The districts of the Chinese Empire which produce rhubarb extend over a vast area. They are comprised in the four northern provinces of China Proper, known as Chihli, Shansi, Shensi, and Honan; the immense north-western province of Kansuh, formerly partly included in Shensi, but now extending across the desert of Gobi and to the frontiers of Tibet; the province of Tsing-hai inhabited by Mongols, which includes the great salt lake of Koko-nor and the districts of Tangut, Sifan, and Turfan; and lastly the mountains of the western province of Szechuen. The plant is found on the pasturages of the high plateaux, growing particularly well on spots that have been enriched by encampments.

What little we know regarding the production of rhubarb and its preparation for the market, from Catholic missionaries, is of a rather meagre and unsatisfactory character. The root is dug up at the beginning of autumn when the vegetation of the plant is on the decline, and the operation is probably continued for a few months, or in some districts for the whole winter. It is cleaned, its cortical part sliced off, and the root cut into pieces for drying. This is performed either by the aid of fire-heat, or by simple exposure to sun and air, or the pieces are first partially dried on a hot stone, and then strung on a cord and suspended until the desiccation is complete.

According to F. von Richthofen the best rhubarb is collected exclusively from plants growing wild in the high alps of western Szechuen, especially in the Bayankara range, between the sources of the Hoang-ho and the rivers Ya-lung-Kiang and Min-Kiang. This variety is chiefly known under the name Shensi rhubarb, although the inhabitants of the province of Szechuen pretend the superiority of the drug of their own country. The important places for the commodity are Sining-fu in the province of Kansu, and Kwan-hien in Szechuen. In the plain of Tshing-tu-fu, according to Richthofen, rhubarb is cultivated in fields, but its product is stated to be much inferior to that of the true plant which is said not to succeed under culture.

Rhubarb is now purchased for the European market chiefly at Hankow on the upper Yangtsze, whither it is brought from the provinces of Shensi, Kansu, and Szechuen. From Hankow it is sent down to Shanghai, and there shipped for Europe. The exports from Hankow are stated in official documents to have amounted to the following numbers of peculs (one pecul = 133⅓ lb. = 60·479 kilogrammes):

1866 1867 1868 1869 1870 1871 1872

2985 3425 2866 3398 3370 3859 3167

In 1877 there were exported by way of Hankow 2096 peculs from Shensi and 3385 peculs from Szechuen.—From all the Chinese ports, 5124 peculs of rhubarb were shipped in 1874.

Much smaller quantities (554 peculs in 1872, 1055 peculs in 1874) are shipped from Tientsin; and there are occasional exportations from Canton, Amoy, Foochow, and Ningpo. The imports of rhubarb into the United Kingdom in 1870 amounted to 343,306 lb., the estimated value of which was £62,716.

We have no information about the rhubarb which is stated by Bellew to grow on the hills near Kayn or Ghayn in eastern Persia (about 32½° N. lat.).

Description—China Rhubarb as imported into Europe consists of portions of a massive root which display considerable diversity of form, arising from the various operations of paring, slicing and trimming, to which they have been subjected. Thus some pieces are cylindrical or rather barrel-shaped, others conical, while a large proportion are plano-convex, and others again are of no regular shape. These forms are not all found in the same package, the drug being usually sorted into round and flat rhubarb. In dimensions we find 3 to 4 inches the commonest length, though an occasional piece 6 inches long or more may be met with. The width may be stated at 2 to 3 inches. The outer surface of the root is somewhat shrivelled, often exhibiting portions of a dark bark that have not been pared away. Many pieces are pierced with a hole, in which may be found the remains of a cord used to suspend the root while drying. The drug is dusted over with a bright brownish-yellow powder, on removal of which the outer side of the root is seen to have a rusty-brown hue, or viewed with a lens to be marked by the medullary rays, which appear as an infinity of short broken lines of deep brown, traversing a white ground.

The character which most readily distinguishes the rhubarb of China is that well-developed pieces, broken transversely, display these dark lines arranged as an internal ring of star-like spots. Although this character is by no means obvious in every piece of Chinese rhubarb, it is of some utility from the fact that in European rhubarb, such spots are generally wholly wanting, or at most occur only sparingly and in an isolated manner.

In judging of rhubarb, great stress is laid upon the appearance of the root when broken, and the circumstance of the fractured surface presenting no symptoms of decay, discoloration, or sponginess. In good rhubarb, the interior is found to be compact, and beautifully veined with reddish-brown and white, sometimes not unmixed with iron-grey. The root when chewed tastes gritty, by reason of the crystals it contains of oxalate of calcium; but it is besides bitter, astringent and nauseous. The odour is peculiar, and except by the druggist, is mostly regarded as very disagreeable.

Microscopic Structure—The tissue of rhubarb is made up of a white parenchyme, brown medullary rays and a few irregularly scattered very large fibro-vascular bundles, which are devoid of ligneous cells.

On a transverse fracture of specimens, which are not too much peeled, a narrow dark cambial zone may be distinguished. In that part of the root, only the medullary rays display the usual radial arrangement, and in the interior of the root no regular structure is met with. There is no well-marked pith, but the central portion of the tissue shows a mixture of white parenchyme and brown medullary rays running in every direction. In full-grown roots, the central part is separated from the cambial zone by the band of stellate patches already mentioned.

As to the contents of the white cells, they are loaded either with starch or tufted crystals of oxalate of calcium, the amount of the latter being especially liable to variation. Scheele, after having discovered the oxalic acid, pointed out in 1784 that the crystals under notice consist of that acid in combination with lime; he was the first to point out the true composition of those crystals which are of so wide a distribution throughout the vegetable kingdom. The medullary rays contain the substances peculiar to rhubarb, but none of them occur in a crystalline state.

Chemical Composition—The active constituent of the root has long been supposed to reside in the yellowish-red contents of the medullary rays. Schrader as early as 1807 prepared a Rhubarb-Bitter, to which he attributed the medicinal powers of the drug. Since then several substances of the same kind have been separated by various methods, and described under different names: such are the Rhabarberstoff of Trommsdorff, the Rheumin of Hornemann, the Rhabarberin of Buchner and Herberger, the Rhubarb-Yellow or Rheïn, and the Rhabarbaric Acid of Brandes.

Schlossberger and Döpping in 1844 first recognized among the above-named substances a definite chemical body named Chrysophan or Chrysophanic Acid,

C₁₄H₅ CH₃ O₂,

(OH)₂

which had been found in 1843 by Rochleder and Heldt in the yellow lichen, Parmelia parietina. It partly forms the yellow contents of the medullary rays of rhubarb, and when isolated crystallizes in golden yellow needles or in plates. It dissolves in ether, alcohol, or benzol; though scarcely soluble in water, it is nevertheless extracted from the root to some extent by that solvent, probably by reason of some accompanying substance. Alkalis dissolve it, forming fine dark red solutions. Chrysophan, C₁₅H₁₀O₄, is a derivative of anthracene, C₁₄H₁₀, and closely allied to alizarin, C₁₄H₈O₄.

By precipitating alcoholic solutions of extract of rhubarb with ether, Schlossberger and Döpping obtained, together with chrysophan, resinous bodies which they named Aporetin, Phæoretin and Erythroretin.

De la Rue and Müller (1857) extracted from rhubarb, in addition to chrysophan, an allied substance, Emodin, which crystallizes in orange-coloured prisms, sometimes as much as two inches long. Its constitution was subsequently found to agree with the formula

C₁₄H₄ CH₃ O₂.

(OH)₃

Kubly (1867) has obtained from rhubarb the following constituents:—

1. Rheo-tannic Acid, C₂₆H₂₆O₁₄, a yellowish powder abundantly present in rhubarb, soluble in water or alcohol, not in ether. Its solutions produce blackish-green precipitates with persalts of iron, and greyish ones slowly turning blue, with protosalts of the same.

2. Rheumic Acid (Rheumsäure), C₂₀H₁₆O₉, obtained as a reddish-brown powder, by boiling rheo-tannic acid with a dilute mineral acid, a fermentable sugar being developed at the same time. Rheumic acid exhibits nearly the same reactions as rheo-tannic acid, but is very sparingly soluble in cold water. It partly pre-exists in rhubarb.

3. Neutral colourless substance, sparingly soluble in hot water, and separating from the latter in prismatic crystals of the formula C₁₀H₁₂O₄; no name has yet been given to it. A “white crystalline resin” (and a dark brown crystalline resin) has been isolated in 1878 by Dragendorff.

4. Phæoretin, C₁₆H₁₆O₇, agreeing with the substance thus named by Schlossberger and Döpping. It is a brown powder, soluble in alcohol or in acetic acid, but not in ether, chloroform or water.

5. Chrysophan, described above.

According to Dragendorff (1878) mucilaginous matters occur in the different varieties of rhubarb to the amount of from 11 to 17 per cent. He states them to consist of mucilage (properly so called), arabic acid, metarabic acid and pararabin, and moreover enumerates also pectose among the constituents of the drug.

Small quantities of albuminoid substances, malic acid, fat and sugar have also been met with in rhubarb. As to its mineral constituents, their amount is exceedingly variable. Two samples of good China Rhubarb dried at 100° C. and incinerated, yielded us respectively 12·9 and 13·87 per cent. of ash. Another sample, which we had particularly selected on account of its pale tint, afforded no less than 43·27 per cent. of ash. The ash consists of carbonates of calcium and potassium. English rhubarb from Banbury (portions of a large specimen) left after incineration 10·90 per cent. of ash.

From a practical point of view the chemical history of rhubarb is far from satisfactory, for we are still ignorant to what principle the drug owes its therapeutic value, or what are the pharmaceutical preparations in which the active matter may be most appropriately exhibited. Chrysophan is said to act as a purgative, but less powerfully than rhubarb itself.

Uses—Rhubarb is one of the commonest and most valuable purgatives; it is also taken as a stomachic and tonic.

Substitutes—These are found in the roots of the various species of Rheum cultivated in Europe. In most countries, the cultivation of rhubarb for medicinal use has at some time been attempted. Yet in but few instances has it been persistently carried on; and though the drug produced has often been of good appearance, it has failed to gain the confidence of medical men, and to acquire much importance in the drug-market. The European rhubarb most interesting from our point of view is

English Rhubarb—So early as 1535, Andrew Boorde, an English Carthusian monk and practitioner of medicine, obtained seeds of rhubarb, which he sent as “a grett tresure” to Sir Thomas Cromwell, Secretary of State to Henry VIII.; but as he says they “come owtt of barbary” we must be allowed to hold their genuineness as doubtful.

In the following century, namely about the year 1608, Prosper Alpinus of Padua cultivated as the True Rhubarb a plant which is now known as Rheum Rhaponticum L., a native of Southern Siberia and the regions of the Volga. From this stock, Sir Matthew Lister, physician to Charles I., procured seeds when in Italy, and gave them to Parkinson, who raised plants from them.

Collinson obtained rhubarb plants from seeds procured in Tartary, and sent to him in 1742 by Professor Siegesbeck of St. Petersburg.

About 1777 Hayward, an apothecary of Banbury in Oxfordshire, commenced the cultivation of rhubarb with plants of Rh. Rhaponticum, raised from seeds sent from Russia in 1762. The drug he produced was so good that the Society of Arts awarded him in 1789 a silver medal, and in 1794 a gold medal. The Society also awarded medals about the same time (1789-1793) to growers of rhubarb in Somersetshire, Yorkshire, and Middlesex, some of whom, it appears, cultivated Rh. palmatum. On the death of Hayward in 1811, his rhubarb plants came into the possession of Mr. P. Usher, by whose descendants, Mr. R. Usher and sons, they are still cultivated at Bodicott, a village near Banbury.

The authors of this book had the pleasure of inspecting the rhubarb fields of Messrs. Usher on Sept. 4, 1872, and of seeing the whole process of preparing the root for the market. The land under cultivation is about 17 acres, the soil being a rich friable loam. The roots are taken from the ground during the autumn up to the month of November. It is considered advantageous that they should be 6 or 7 years old, but they are seldom allowed to attain more than 3 or 4 years. The clumps of root as removed from the field to the yard, where the trimming takes place, are of huge size, weighing with the earth attached to them as much as 60 or 70 lb. They are partially cleaned, the smaller roots are cut off, and the large central portion is rapidly trimmed into a short, cylindrical mass the size of a child’s head. This latter subsequently undergoes a still further paring, and is finally sliced longitudinally; the other and less valuable roots are also pared, trimmed, and assorted according to size. The fresh roots are fleshy, easily cut, and of a beautiful deep yellow. All are dried in buildings constructed for the purpose, and heated by flues. The drying occupies several weeks. The root after drying has a shrivelled, unsightly appearance, which may be remedied by paring and filing. The finished drug has to be stored in a warm dry place.

When well prepared, Banbury rhubarb is of excellent appearance. The finest pieces, which are semi-cylindrical, are quite equal in size to the drug of China. The colour is as good, and the fractured surface exhibits pink markings not less distinct and brilliant. Even the smaller roots, which are dried as sticks, have internally a good colour, and afford a fine powder. But the odour is somewhat different from that of Chinese rhubarb; the taste is less bitter but more mucilaginous and astringent, and the root is of a more spongy, soft, and brittle texture. The structure is the same as that of the Chinese rhubarb, except that, as already stated, the star-like spots, if present, are isolated, and not arranged in a regular zone.

The drug commands but a low price, and is chiefly sold, it is said, for exportation in the state of powder. It is not easily purchased in London.