Froude's _Life_, by Herbert Paul, was published in 1905. (W. Hu.)

FRUCTOSE, LAEVULOSE, or FRUIT-SUGAR, a carbohydrate of the formula

C6H12O6. It is closely related to ordinary d-glucose, with which it

occurs in many fruits, starches and also in honey. It is a hydrolytic

product of inulin, from which it may be prepared; but it is more usual

to obtain it from "invert sugar," the mixture obtained by hydrolysing

cane sugar with sulphuric acid. Cane sugar then yields a syrupy mixture

of glucose and fructose, which, having been freed from the acid and

concentrated, is mixed with water, cooled in ice and calcium hydroxide

added. The fructose is precipitated as a saccharate, which is filtered,

suspended in water and decomposed by carbon dioxide. The liquid is

filtered, the filtrate concentrated, and the syrup so obtained washed

with cold alcohol. On cooling the fructose separates. It may be obtained

as a syrup, as fine, silky needles, a white crystalline powder, or as a

granular crystalline, somewhat hygroscopic mass. When anhydrous it melts

at about 95 deg. C. It is readily soluble in water and in dilute alcohol,

but insoluble in absolute alcohol. It is sweeter than cane sugar and is

more easily assimilated. It has been employed under the name diabetin as

a sweetening agent for diabetics, since it does not increase the

sugar-content of the urine; other medicinal applications are in phthisis

(mixed with quassia or other bitter), and for children suffering from

tuberculosis or scrofula in place of cane sugar or milk-sugar.

Chemically, fructose is an oxyketone or ketose, its structural formula

being CH2OH.(CH.OH)3.CO.CH2OH; this result followed from its conversion

by H. Kiliani into methylbutylacetic acid. The form described above is

_laevo_-rotatory, but it is termed d-fructose, since it is related to

d-glucose. Solutions exhibit mutarotation, fresh solutions having a

specific rotation of -104.0 deg., which gradually diminishes to -92 deg.

It was synthesized by Emil Fischer, who found the synthetic sugar which

he named [alpha]-acrose to be (d + l)-fructose, and by splitting this

mixture he obtained both the d and l forms. Fructose resembles d-glucose

in being fermentable by yeast (it is the one ketose which exhibits this

property), and also in its power of reducing alkaline copper and silver

solutions; this latter property is assigned to the readiness with which

hydroxyl and ketone groups in close proximity suffer oxidation. For the

structural (stereochemical) relations of fructose see SUGAR.

FRUGONI, CARLO INNOCENZIO MARIA (1692-1768), Italian poet, was born at

Genoa on the 21st of November 1692. He was originally destined for the

church and at the age of fifteen, in opposition to his strong wishes,

was shut up in a convent; but although in the following year he was

induced to pronounce monastic vows, he had no liking for this life. He

acquired considerable reputation as an elegant writer both of Latin and

Italian prose and verse; and from 1716 to 1724 he filled the chairs of

rhetoric at Brescia, Rome, Genoa, Bologna and Modena successively,

attracting by his brilliant fluency a large number of students at each

university. Through Cardinal Bentivoglio he was recommended to Antonio

Farnese, duke of Parma, who appointed him his poet laureate; and he

remained at the court of Parma until the death of Antonio, after which

he returned to Genoa. Shortly afterwards, through the intercession of

Bentivoglio, he obtained from the pope the remission of his monastic

vows, and ultimately succeeded in recovering a portion of his paternal

inheritance. After the peace of Aix-la-Chapelle he returned to the court

of Parma, and there devoted the later years of his life chiefly to

poetical composition. He died on the 20th of December 1768. As a poet

Frugoni was one of the best of the school of the Arcadian Academy, and

his lyrics and pastorals had great facility and elegance.

His collected works were published at Parma in 10 vols. in 1799, and a

more complete edition appeared at Lucca in the same year in 15 vols. A

selection from his works was published at Brescia in 1782, in 4 vols.

FRUIT (through the French from the Lat. _fructus_; _frui_, to enjoy), in

its widest sense, any product of the soil that can be enjoyed by man or

animals; the word is so used constantly in the Bible, and extended, as a

Hebraism, to offspring or progeny of man and of animals, in such

expressions as "the fruit of the body," "of the womb," "fruit of thy

cattle" (Deut. xxviii. 4), &c., and generally to the product of any

action or effort. Between this wide and frequently figurative use of the

word and its application in the strict botanical sense treated below,

there is a popular meaning, regarding the objects denoted by the word

entirely from the standpoint of edibility, and differentiating them

roughly from those other products of the soil, which, regarded

similarly, are known as vegetables. In this sense "fruit" is applied to

such seed-envelopes of plants as are edible, either raw or cooked, and

are usually sweet, juicy or of a refreshing flavour. But applications of

the word in this sense are apt to be loose and shifting according to the

fashion of the time.

Fruit, in the botanical sense, is developed from the flower as the

result of fertilization of the ovule. After fertilization various

changes take place in the parts of the flower. Those more immediately

concerned in the process, the anther and stigma, rapidly wither and

decay, while the filaments and style often remain for some time; the

floral envelopes become dry, the petals fall, and the sepals are either

deciduous, or remain persistent in an altered form; the ovary becomes

enlarged, forming the _pericarp_; and the ovules are developed as the

seeds, containing the embryo-plant. The term fruit is strictly applied

to the mature pistil or ovary, with the seeds in its interior; but it

often includes other parts of the flower, such as the bracts and floral

envelopes. Thus the fruit of the hazel and oak consists of the ovary

enveloped by the bracts; that of the apple and pear, of the ovary and

floral receptacle; and that of the pine-apple, of the whole

inflorescence. Such fruits are sometimes distinguished as _pseudocarps_.

In popular language, the fruit includes all those parts which exhibit a

striking change as the result of fertilization. In general, the fruit is

not ripened unless fertilization has been effected; but cases occur as

the result of cultivation in which the fruit swells and becomes to all

appearance perfect, while no seeds are produced. Thus, there are

seedless oranges, grapes and pineapples. When the ovules are

unfertilized, it is common to find that the ovary withers and does not

come to maturity; but in the case of bananas, plantains and bread-fruit,

the non-development of seeds seems to lead to a larger growth and a

greater succulence of fruit.

The fruit, like the ovary, may be formed of a single carpel or of

several. It may have one cell or cavity, being _unilocular_; or many,

_multilocular_, &c. The number and nature of the divisions depend on

the number of carpels and the extent to which their edges are folded

inwards. The appearances presented by the ovary do not always remain

permanent in the fruit. Great changes are observed to take place, not

merely as regards the increased size of the ovary, its softening or

hardening, but also in its internal structure, owing to the

suppression, additional formation or enlargement of parts. Thus, in

the ash (fig. 1) an ovary with two cells, each containing an ovule

attached to a central placenta, is changed into a unilocular fruit

with one seed; one ovule becomes abortive, while the other, g,

gradually enlarging until the septum is pushed to one side, unites

with the walls of the cell, and the placenta appears to be parietal.

In the oak and hazel, an ovary with three and two cells respectively,

and two ovules in each, produces a one-celled fruit with one seed. In

the coco-nut, a trilocular and triovular ovary produces a one-celled,

one-seeded fruit. This abortion may depend on the pressure caused by

the development of certain ovules, or it may proceed from

non-fertilization of all the ovules and consequent non-enlargement of

the carpels. Again, by the growth of the placenta, or the folding

inwards of parts of the carpels, divisions occur in the fruit which

did not exist in the ovary. In _Cathartocarpus Fistula_ a one-celled

ovary is changed into a fruit having each of its seeds in a separate

cell, in consequence of spurious dissepiments being produced

horizontal from the inner wall of the ovary. In flax (_Linum_) by the

folding inwards of the back of the carpels a five-celled ovary becomes

a ten-celled fruit. In _Astragalus_ the folding inwards of the dorsal

suture converts a one-celled ovary into a two-celled fruit; and in

_Oxytropis_ the folding of the ventral suture gives rise to a similar

change. The development of cellular or pulpy matter, and the

enlargement of parts not forming whorls of the flower, frequently

alter the appearance of the fruit, and render it difficult to discover

its formation. In the gooseberry (fig. 29), grape, guava, tomato and

pomegranate, the seeds nestle in pulp formed by the placentas. In the

orange the pulpy matter surrounding the seeds is formed by succulent

cells, which are produced from the inner partitioned lining of the

pericarp. In the strawberry the receptacle becomes succulent, and

bears the mature carpels on its convex surface (fig. 2); in the rose

there is a fleshy hollow receptacle which bears the carpels on its

concave surface (fig. 3). In the juniper the scaly bracts grow up

round the seeds and become succulent, and in the fig (fig. 4) the

receptacle becomes succulent and encloses an inflorescence.

[Illustration:

Fig. 1.--Samara or winged fruit of Ash (_Fraxinus_). 1, Entire, with

its wing a; 2, lower portion cut transversely, to show that it

consists of two cells; one of which, l, is abortive, and is reduced

to a very small cavity, while the other is much enlarged and filled

with a seed g.

Fig. 2.--Fruit of the Strawberry (_Fragaria vesca_), consisting of

an enlarged succulent receptacle, bearing on its surface the small

dry seed-like fruits (achenes). (After Duchartre.)

From Strasburger's _Lehrbuch der Botanik_, by permission of Gustav

Fischer.

Fig. 3.--Fruit of the Rose cut vertically. s', Fleshy hollowed

receptacle; s, persistent sepals; _fr_, ripe carpels; e, stamens,

withered.

Fig. 4.--Peduncle of Fig (_Ficus Carica_), ending in a hollow

receptacle enclosing numerous male and female flowers.

Fig. 5.--Fruit of Cherry (_Prunus Cerasus_) in longitudinal section.

ep, Epicarp; m, mesocarp; en, endocarp.

From Strasburger's _Lehrbuch der Botanik_, by permission of Gustav

Fischer.]

The pericarp consists usually of three layers, the external, or

_epicarp_ (fig. 5, ep); the middle, or _mesocarp_, m; and the

internal, or _endocarp_, _en_. These layers are well seen in such a

fruit as the peach, plum or cherry, where they are separable one from

the other; in them the epicarp forms what is commonly called the skin;

the mesocarp, much developed, forms the flesh or pulp, and hence has

sometimes been called _sarcocarp_; while the endocarp, hardened by the

production of woody cells, forms the _stone_ or _putamen_ immediately

covering the kernel or seed. The pulpy matter found in the interior of

fruits, such as the gooseberry, grape and others, is formed from the

placentas, and must not be confounded with the sarcocarp. In some

fruits, as in the nut, the three layers become blended together and

are indistinguishable. In bladder senna (_Colutea arborescens_) the

pericarp retains its leaf-like appearance, but in most cases it

becomes altered both in consistence and in colour. Thus in the date

the epicarp is the outer brownish skin, the pulpy matter is the

mesocarp or sarcocarp, and the thin papery-like lining is the endocarp

covering the hard seed. In the medlar the endocarp becomes of a stony

hardness. In the melon the epicarp and endocarp are very thin, while

the mesocarp forms the bulk of the fruit, differing in texture and

taste in its external and internal parts. The rind of the orange

consists of epicarp and mesocarp, while the endocarp forms partitions

in the interior, filled with pulpy cells. The part of the pericarp

attached to the peduncle is the base, and the point where the style or

stigma existed is the apex. This latter is not always the apparent

apex, as in the case of the ovary; it may be lateral or even basilar.

The style sometimes remains in a hardened form, rendering the fruit

_apiculate_; at other times it falls off, leaving only traces of its

existence. The presence of the style or stigma serves to distinguish

certain single-seeded pericarps from seeds.

[Illustration:

FIG. 6.--Seed-vessel or capsule of Campion, opening by ten teeth at

the apex. The calyx c is seen surrounding the seed-vessel.

FIG. 7.--Capsule of Poppy, opening by pores p, under the radiating

peltate stigma s.]

Dehiscence of fruits.

When the fruit is mature and the seeds are ripe, the carpels usually

give way either at the ventral or dorsal suture or at both, and so

allow the seeds to escape. The fruit in this case is _dehiscent_. But

some fruits are _indehiscent_, falling to the ground entire, and the

seeds eventually reaching the soil by their decay. By dehiscence the

pericarp becomes divided into different pieces, or _valves_, the fruit

being univalvular, bivalvular or multivalvular, &c., according as

there are one, two or many valves. The splitting extends the whole

length of the fruit, or is partial, the valves forming teeth at the

apex, as in the order Caryophyllaceae (fig. 6). Sometimes the valves

are detached only at certain points, and thus dehiscence takes place

by pores at the apex, as in poppy (fig. 7), or at the base, as in

_Campanula_. Indehiscent fruits are either dry, as the nut, or fleshy,

as the cherry and apple. They are formed of one or several carpels. In

the former case they usually contain only a single seed, which may

become so incorporated with the pericarp as to appear to be naked, as

in the grain of wheat and generally in grasses. In such cases the

presence of the remains of style or stigma determines their true

nature.

[Illustration:

FIG. 8.--Dry dehiscent fruit. The pod (legume) of the Pea; r, the

dorsal suture; b, the ventral; c, calyx; s, seeds.

From Vines' _Students' Text-Book of Botany_, by permission of Swan

Sonnenschein & Co.

FIG. 9.--(1) Fruit or capsule of Meadow Saffron (_Colchicum

autumnale_), dehiscing along the septa (septicidally); (2) same cut

across, showing the three chambers with the seeds attached along the

middle line (axile placentation).

FIG. 10.--Diagram to illustrate the septicidal dehiscence in a

pentalocular capsule. The loculaments l correspond to the number of

the carpels, which separate by splitting through the septa, s.

FIG. 11.--The seed vessel (capsule) of the Flower-de-Luce (_Iris_),

opening in a loculicidal manner. The three valves bear the septa in

the centre, and the opening takes place through the back of the

loculaments. Each valve is formed by the halves of contiguous

carpels.

FIG. 12.--Diagram to illustrate loculicidal dehiscence. The

loculaments l, split at the back, and the valves separate, bearing

the septa s on their centres.

FIG. 13.--Diagram to illustrate septifragal dehiscence, in which the

dehiscence takes place through the back of the loculaments l, and

the valves separate from the septa s, which are left attached to the

placentas in the centre.]

Dehiscent fruits, when composed of single carpels, may open by the

ventral suture only, as in the paeony, hellebore, _Aquilegia_ (fig.

28) and _Caltha_; by the dorsal suture only, as in magnolias and some

_Proteaceae_, or by both together, as in the pea (fig. 8) and bean; in

these cases the dehiscence is _sutural_. When composed of several

united carpels, two types of dehiscence occur--a longitudinal and a

transverse. In the longitudinal the separation may take place by the

dissepiments throughout their length, so that the fruit is resolved

into its original carpels, and each valve represents a carpel, as in

rhododendron, _Colchicum_, &c.; this dehiscence, in consequence of

taking place through the septum, is called _septicidal_ (figs. 9, 10).

The valves separate from their commissure, or central line of union,

carrying the placentas with them, or they leave the latter in the

centre, so as to form with the axis a column of a cylindrical, conical

or prismatic shape. Dehiscence is _loculicidal_ when the union between

the edges of the carpels is persistent, and they dehisce by the dorsal

suture, or through the back of the loculaments, as in the lily and

iris (figs. 11, 12). In these cases each valve consists of a half of

each of two contiguous carpels. The placentas either remain united to

the axis, or they separate from it, being attached to the septa on the

valves. When the outer walls of the carpels break off from the septa,

leaving them attached to the central column, the dehiscence is said to

be _septifragal_ (fig. 13), and where, as in _Linum catharticum_ and

_Calluna_, the splitting takes place first of all in a septicidal

manner, the fruit is described as _septicidally septifragal_; while in

other cases, as in thorn apple (_Datura Stramonium_), where the

splitting is at first loculicidal, the dehiscence is _loculicidally

septifragal_. In all those forms the separation of the valves takes

place either from above downwards or from below upwards. In

_Saxifraga_ a splitting for a short distance of the ventral sutures of

the carpels takes place, so that a large apical pore is formed. In the

fruit of Cruciferae, as wallflower (fig. 14), the valves separate from

the base of the fruit, leaving a central _replum_, or frame, which

supports the false septum formed by a prolongation from the parietal

placentas on opposite sides of the fruit, extending between the

ventral sutures of the carpels. In Orchidaceae (fig. 15) the pericarp,

when ripe, separates into three valves in a loculicidal manner, but

the midribs of the carpels, to which the placentas are attached, often

remain adherent to the axis both at the apex and base after the valves

bearing the seeds have fallen. The other type of dehiscence is

transverse, or _circumscissile_, when the upper part of the united

carpels falls off in the form of a lid or operculum, as in _Anagallis_

and in henbane (_Hyoscyamus_) (fig. 16).

[Illustration:

FIG. 14.--Siliqua or seed-vessel of Wallflower (_Cheiranthus

Cheiri_), opening by two valves, which separate from the base

upwards, leaving the seeds attached to the dissepiment which is

supported by the replum.

From Strasburger's _Lehrbuch der Botanik_, by permission of Gustav

Fischer.

FIG. 15.--Capsule of an Orchid (_Xylobium_). v, valve.

FIG. 16.--Seed-vessel of _Anagallisarvensis_, opening by

circumscissile dehiscence.

From Strasburger's _Lehrbuch der Botanik_, by permission of Gustav

Fischer.

FIG. 17.--Lomentum of _Hedysarum_ which, when ripe, separates

transversely into single-seeded portions or mericarps.

Encyclopaedia Britannica, 11th Edition, "Frost" to "Fyzabad" Volume 11, Slice 3 · 第 6 / 72 题