With regard to their _apex_, the bile-vessels are sometimes _fixed_

singly or connectedly to the intestine merely by a few muscular fibres;

for they do not enter it, their ends having no orifice. This structure

is mostly to be met with in the _Coleoptera_[486]. In caterpillars,

the tops of these vessels perforate the outer skin of the rectum, and

proceeding in dense convolutions to the anus, become at last so fine

that their terminations cannot be discovered[487]. In other cases,

the extremities of a pair of these vessels _unite_ so as to form a

double one: this may be seen in those of _Philonthus politus_[488], and

probably other rove-beetles: and lastly, in others the bile-vessels are

_free_, hanging down by the intestinal canal, without being attached

to it or to each other. This structure is constantly found in the

_Orthoptera_ and _Hymenoptera_ Orders, &c.[489].

With regard to their _number_, the bile-vessels vary from two to

upwards of one hundred and fifty, yet so that their whole amount is

constantly the product of the number two,--at least as far as they

have been counted: and even when those on one side are not alike,

a similar variation takes place in the other, as may be seen in

_Galleruca Vitellinæ_, where on each side are two long ones and one

shorter[490]; the most usual numbers are, _four_--_six_--or _many_,

that is, more than _twenty_--

_Two_ bile-vessels are found in the larva of _Cetonia aurata_[491].

_Four_ most _Coleoptera_, _Diptera_,

and _Hemiptera_[492].

_Six_ _Lepidoptera_, some _Coleoptera_[493],

&c.

_Eight_ _Myrmeleon_, _Hemerobius_[494].

_Fourteen_ _Formica rufa_[495].

_Twenty_ larva of _Clavellaria Amerinæ_[496].

_Many_ _Libellulina_, _Orthoptera_, and

_Hymenoptera_[497].

The bile-vessels vary considerably in _length_: in many cases where

they are _free_ they are _short_[498]; they are often very long,

and perhaps those that are _fixed_ may be generally stated as the

longest. In the Lamellicorn beetles they are remarkable for their

great length[499].

Having given you this general account of the intestinal canal and its

parts and appendages, I shall now state some of the peculiarities

that in this respect distinguish particular tribes and families.

The _Coleoptera_ alone, exhibit as many variations in the

structure of the alimentary tube as all the other Orders of

insects together:--to particularize these would occupy too large

a portion of this letter, I shall therefore only notice a few

of the most remarkable. In general they may be stated as having

universally a stomach, a small intestine and rectum, and not more

than _three_ pairs of _fixed_ or _united_ bile-vessels. In the

Predaceous beetles, the _gullet_ mostly widens at the base into a

considerable _crop_, followed by a _gizzard_, a shaggy _stomach_,

and two pairs of _united_ bile-vessels. The whole alimentary canal

in these, is never less than _double_, and sometimes _treble_ the

length of the body[500]. In the _carnivorous_ beetles, at least the

_Staphylinidæ_ and _Silphidæ_, there is little or no _crop_, and

the _gizzard_ is hidden: in the former, the whole length of the

intestinal canal is not _twice_, while in the latter it is more than

_four_ times that of the body[501]. In these also the intermediate

portion of the large intestine is singularly annulated[502]. In the

_Petalocera_ the _stomach_ is usually longer than all the rest of

the intestines together, and often convoluted: in the cockchafer

the whole intestinal canal is nearly _five_ times the length of the

body, _four_ parts of which is occupied by the stomach[503]. In

the grub the canal scarcely exceeds the length of the animal[504].

In _Lampyris_ the stomach exhibits a remarkable appearance, having

on each side a series of spherical _folds_ or _vesicles_[505].

Have these any thing to do with the secretion of its phosphoric

matter? _Tenebrio_ has a _gizzard_ armed internally with calluses,

and a shaggy stomach, and _Blaps_ does not differ materially;

their entire canal is more than twice the length of the body[506].

In the _vesicatory_ beetles (_Cantharis_, _Meloe_, &c.) there is

no _gizzard_, and the canal is less than twice the length of the

body[507]. Little is known with regard to the alimentary canal of

the beetles distinguished by a _rostrum_ (_Rhyncophora_). In the

only two that appear to have been examined, _Rhynchites Betuleti_ and

_Cryptorhynchus Lapathi_, that canal is moderately long, the stomach

partially shaggy, and the small intestine inversely claviform; but

in other respects they differ materially[508]. In the former there

is no crop or gizzard, the stomach is fringed on each side, except

at its upper extremity, with a series of small _cœca_ or shags, and

there are _three_ pairs of bile-vessels[509]; while in the latter

the gullet is dilated into a crop which includes a gizzard in which

the skill of a DIVINE artist is singularly conspicuous:--though

so minute as scarcely to exceed a large pin's head in size, it is

stated to be armed internally with more than 400 pairs of teeth,

moved by an infinitely greater number of muscles[510]. A transverse

section of this gizzard represents two concentric stars, with nine

rays each[511]: the object of this structure is, the comminution

of the timber which this beetle has to perforate and probably

devour[512]. The stomach is very slender, but dilates in the middle

into a spherical vesicle[513], and there are only two pairs of

bile-vessels[514]. In the _Capricorn_ beetles, the part we are

considering varies much: in general we may observe that it is more

than _double_ the length of the body, that the stomach is long

and slender, and usually naked, that the gullet terminates in a

crop without a distinct gizzard, and that there are _three_ pairs

of bile-vessels[515]. In the Herbivorous beetles (_Chrysomela_,

_Cassida_, &c.) the canal is more than double the length of the

body, and in some much longer[516], the stomach is long, and commonly

naked; but in _Chrysomela violacea_ it is covered with hemispherical

prominences[517], and in _Chrysomela Populi_ it is shaggy[518]; in

the insect last named and _Galleruca Vitellinæ_ the rectum consists

of _two_ pieces[519]. In this tribe the intestines of the larva

resemble those of the perfect insect[520].

In the _Orthoptera_ the alimentary canal, which continues the same in

every state, is short, or only moderately long; the gullet has one

or two lateral pouches or crops[521], and terminates in a gizzard

of curious construction, with singular folds and teeth[522]; then

follows a short stomach, usually with a pair or more of _cœca_ at its

upper extremity[523]; the lower intestines are not distinct, and the

bile-vessels numerous, short and free[524].

In the _Neuroptera_, many of the genera are distinguished by the

remarkable length of the gullet, and by the lower intestines forming

one short piece[525]. In the _Libellulina_ the bile-vessels are

numerous, short, and free, as in the _Orthoptera_[526]. In _Hemerobius_

and _Myrmeleon_ there is a gizzard[527], and just above it a _cœcum_,

in the former very remarkable, is connected with the gullet[528].

The _Hymenoptera_ appear all to be distinguished by a long slender

gullet, terminating in a dilated crop forming the honey-bag; their

stomach is variable, their small intestine slender, and the rectum

dilated;--their bile-vessels, like those of the two preceding

Orders, are numerous, short, and free[529]. In the ants and

ichneumons there is an approach to a gizzard[530]. In the wasp and

humble-bee the stomach is very long, with muscular rings surrounding

it[531]. In this Order the larvæ at first have no lower intestines

and void no excrement[532], but as they approach to the pupa state

one begins to appear[533].

The next insects whose alimentary canal we are to consider, are those

which, taking their food by _suction_, have no occasion for masticating

organs: this may in part be predicated of the preceding Order, in

which most of the tribes in their perfect state _imbibe_ fluid food,

and use the ordinary organs of _mastication_ principally in operations

connected with their economy; and their crop, in which the honey in

many is stored up for regurgitation, may be regarded in some degree as

analogous to the food-bag of the _Diptera_ and other suctorious insects.

The two sections of the _Hemiptera_ Order differ widely in the canal

we are considering, and I shall therefore give a separate account of

each. In the _Heteropterous_ section, appended to the gullet by a

long convoluted capillary tube, besides the usual saliva-reservoirs

there is often a double vessel, which Ramdohr regards as discharging

the same function, but which in many respects seems rather analogous

to the food-reservoir of the _Diptera_[534]. As I have had no

opportunity of examining this vessel, I shall content myself with

stating this idea, and describe the vessel more fully hereafter. The

gullet, in these, usually terminates in an ample crop consisting

of many folds[535], followed by a long, slender, cylindrical tube,

dilated at its base into a spherical tumour; these two may be said to

form the first stomach: to this succeeds a second[536], which Ramdohr

denominates the _bug_-stomach (_Wanzen-magen_), which varies in its

figure, and in _Pentatoma_ consists of four demi-tubes, so as to form

a quadrangular canal[537]. In the _Homopterous_ section of this Order

Ramdohr seems to have examined but few; _Chermes_ however and _Aphis_

exhibit one remarkable feature; they have _no bile-vessels_, at least

he could discover no trace of these organs[538]. Their intestinal

canal is very simple, their stomach very long, widest above, and

somewhat convoluted, with a very slender gullet[539]. In _Cercopis

spumaria_ the structure is more complex, and extremely singular. It

has _two_ or rather _three_ stomachs; the two first of a _horny_

substance, and the last a slender somewhat convoluted _membranous_

tube, which becoming reversed, is attached by what should be deemed

its lower extremity to the first stomach, from the other side of

which emerge the lower intestines, terminating in a thick pear-shaped

rectum. At the same point of the first stomach the four bile-vessels

are attached, they grow gradually thicker for about a third of their

length, when they become twisted like a cord, and taper towards the

rectum, to which also they are attached[540]. From this structure

it should seem that the food has to pass twice through the first

stomach, before the process of digestion is complete, and it is

rejected at the anus.

The next suctorious Order is the _Lepidoptera_: in these the gullet

is long and slender, surrounded at the beginning with a loose

transparent skin, and at the base furnished with a pair of lateral

sacs, forming the honey-stomach, and probably analogous to the

food-reservoirs of the _Diptera_, which when blown up are of an oval

form; the stomach, as in the bugs, consists of _two_ portions, the

first being the longest[541]. There are three _free_ bile-vessels

on each side, proceeding from a single branch[542]. It will not be

uninteresting here to abstract from Herold the progressive changes

which take place in the intestinal canal in this Order, during the

transition of the animal from the larva to the imago state. In the

_larva_, the gullet, the small intestine, and the rectum, are short

and thick[543], there are a pair of silk reservoirs (_sericteria_),

as well as vessels for the secretion of saliva (_sialisteria_):

if you examine it two days after its first change, you will find

the gullet and the small intestine much lengthened and become very

slender; the stomach contracted both in length and size; the rectum

also changed, and the silk vessels contracted[544]. These in a

_pupa_ eight days old have wholly disappeared; the gullet is become

still longer, its base is dilated into a crop or food-reservoir;

the stomach is still more contracted, and instead of a cylinder

represents a spindle; the small intestine also is lengthened[545]:

at a still more advanced period, when it is near appearing under

its last form, the gullet and small intestine are still more drawn

out; and the honey-bag, though very minute, has become a lateral

appendage of the gullet[546]; and lastly, in the butterfly it appears

as a large vesicle[547]; the small intestine is grown very long[548];

and the rectum has changed its form and acquired a cœcum[549]. When

we consider the adaptation of all these changes of form, the loss

of old organs and the acquisition of new ones, to the new functions

and mode of life of the animal, we see evidently the all-powerful

hand of that ALMIGHTY BEING who created the universe, upholding by

his providence, and the law that he has given to every creature, the

system that he at first brought into existence.

We now come to the _Diptera_. These have a very slender gullet, to

which is attached on one side a long filiform tube, terminating in

the food-reservoir, which in some instances is simple[550], but

most generally consists of two or more vessels[551], collapsing

when empty, but varying in shape and size when inflated with food:

the mouth of the stomach in many cases is dilated into a kind of

ring[552]; sometimes there is on each side a blind appendage or

_cœcum_ opening into it, in _Bombylius_ covered with shags, which

though not connected with the mouth by a tube, Ramdohr regards as

saliva-reservoirs[553]; in _Musca vomitoria_ the beginning of this

organ below the mouth is covered with hemispherical prominences, and

in _Tipula_ it is dilated and marked with transverse folds. There are

usually _two_ pairs of bile-vessels; in the _Muscidæ_ pedunculate

and _free_[554]; in _Tipula_, _Bombylius_, and _Leptis_, sessile

and _united_[555]; and in _Tabanus_ sessile and _fixed_[556]. It is

remarkable that in some of this Order--the reverse of what usually

happens--the alimentary canal appears to be much longer in the larva

than it is in the imago; in _Musca vomitoria_, its length in the

_former_ is two inches and a quarter, while in the _latter_ it is

only one inch and one third[557]. A singular organ distinguishes the

imago of this species, the use of which appears not to be discovered.

It succeeds the _rectum_, and has on each side two short club-shaped

appendages, open at the end, which receive _tracheæ_, and terminate

in a short piece that opens into the anus[558].

In _Hippobosca_ and its affinities the canal in question differs

from that of other _Diptera_, in having no food-reservoir; in other

respects it resembles it[559].

From the above statement it appears that the principal character

which distinguishes those that take their food by _suction_,

from those that _masticate_ it, is the faculty with which they

are furnished by means of an ample crop, honey-stomach, or

food-reservoir, of _regurgitating_ the food they may have stored

up. Another distinction still more striking, which will appear more

evidently hereafter, is to be seen in the _saliva-secretors_ with

which the _suctorious_ tribes are furnished, to be found in very few

_masticators_, by which they are enabled to render the juices more

fluid and fit for suction.

The only insect amongst the _Aptera_ whose alimentary canal I

shall notice, is the common harvest-man (_Phalangium Opilio_): in

this, though the stomach and lower intestine are remarkably simple,

yet their cœcal appendages are numerous and singular: the former,

which has no distinct gullet, is pear-shaped[560]; and the latter,

tapering downwards, and truncated at the end[561]; connected with

it above are no less than twenty-three _cœca_ or blind appendages,

of various forms and dimensions; the last pair but one of which is

very remarkable, being bent like a bow, and furnished externally with

four short clavate processes[562]. It is probable that some of these

organs are analogous to the bile-vessels of other insects.

* * * * *

When the CREATOR in his wisdom fixed the limits of the various tribes

of animals, he united them all into one harmonious system by means

of certain intermediate forms, exhibiting characters taken some

from those that were to precede, and others from those that were

to follow them, and this not only in their _external_ structure,

but likewise in their _internal_ organization; so that we are

not to wonder if in the same individual we meet with organs that

belong to two distinct tribes, or if, remaining nearly the _same_

in their _prima facie_ appearance, they begin to exercise _new_

functions. An instance of this we have seen in the dorsal vessel of

insects, which in the _Arachnida_, though not materially different

in situation or general form, by the addition of a small apparatus

of arteries and veins becomes the centre and fountain of a regular

system of circulation[563]. From the circumstances here alluded to,

physiologists have been led to entertain very different sentiments

with regard to the structure of the alimentary organs of the Class we

are now to enter upon, the _Arachnida_: what some regard as a real

_liver_, others look upon as an _epiploon_ or caul; and what the

last denominate _bile_-vessels are by some of the former considered

as appropriated to the secretion of _chyle_[564]. Yet both these

opinions have some foundation in nature. When, in the _Arachnida_,

we discover a lobular substance consisting of granules filling the

whole cavity of the body and wrapped round the intestines, every one

will see in it no small analogy to the _epiploon_ which in insects

performs the same function: but when, upon a further examination,

we detect certain vessels communicating with this substance and the

intestinal canal[565], the idea that these may be _hepatic ducts_,

and this substance analogous to the _liver_, immediately strikes us

as not improbable. Again: when we discover pairs of other capillary

and tortuous vessels connecting with the intestinal canal either at

the _pylorus_[566] or below it[567], which in appearance strikingly

resemble the bile-vessels which we so constantly find in insects,

we seem warranted in concluding that they are of the same nature

and use: but when a nearer inspection enables us to detect the

hepatic ducts just mentioned in the scorpion, and we find that these

capillary vessels in the spider are in a very different situation

from those in insects which we suppose them to represent, it occurs

to us as not unlikely, that their _function_ may be different.

Let us now consider how the intestinal canal is circumstanced in

the two sections into which the Class _Arachnida_ is divided; the

_Scorpionidea_, and _Araneidea_. In the Scorpions, this organ proceeds

from the mouth to the anus without any flexure or convolution, so that

its length is scarcely equal to that of the body[568]; it is slender,

and its diameter, with the exception of an irregular dilatation here

and there, is nearly the same in its whole extent; the gullet is short;

the stomach long, and nearly cylindrical; the _duodenum_ shorter and

thicker than the stomach, from which, as well as from the _rectum_, it

is separated by a valve; the latter is cylindrical, and opens at the

anus above the insertion of the vesicle that secretes the poison[569].

With regard to the _biliary_ system and its organs: The _liver_ is of

a pulpy granular consistence and of a brownish colour, fills the whole

cavity of the trunk and abdomen, and serves as a bed for the other

intestines. It is divided longitudinally into two portions, by the

channel in which the heart reposes--its anterior part is formed into

many irregular lobes, by the sinuosities of the trunk; at the other

extremity, it terminates in two acute ends, which enter the first joint

of the tail; its surface presents a reticular appearance, the result of

the approximation of polygonous _lobuli_; its interior is a tissue of

infinitely minute glands: in _Scorpio occitanus_ there are about forty

pyramidal _lobuli_ detached from each other, the summits of which, by

their union, form bunches that have their excretory canals, varying in

number in different species, which convey the bile to the alimentary

tube; in the above insect there are six pairs, three in the trunk and

three in the abdomen, and in _S. Europæus_ a smaller number[570]; these

vessels run transversely from the liver, or aggregation of conglomerate

glands, to the intestinal canal[571]; the bunches consist of an

infinite number of spherical glands, generally filled with a brown

thick fluid[572]: besides the transverse vessels, from the base of the

stomach there issue two pairs of very slender tortuous ones, seemingly

analogous to the common bile-vessels; one pair of which runs upwards,

one on each side that organ towards the mouth, forming here and there

some ramifications which enter the liver; and the other runs nearly

transversely to it[573]. As the fluid contained in these vessels is

different from that contained in the glands of the liver, M. Marcel de

Serres supposes they may be chyliferous[574].

In the _Araneidea_ also the alimentary canal is nearly straight,

and scarcely exceeds the length of the body: the _gullet_ is rather

thick and cylindrical[575]; the _stomach_ is distinguished anteriorly

by two pairs of sacs, the upper pair being much the largest and

nearly triangular, the lower linear[576]; from these sacs a narrow

tube runs towards the _rectum_, but which is so entangled with the

liver, muscles, &c., as not to be easily made out[577]; the _rectum_

is rather tumid, and has a lateral _cœcum_[578]. The disposition of

the liver or conglomerate glands is stated to be similar to that of

the scorpion[579]; it is usually white, but in some species it is

yellowish, or reddish, and its lower surface has sometimes regular

excavations[580]; no transverse hepatic ducts connecting it with the

alimentary canal, as in the scorpion, appear to have been at present

discovered: two pairs of capillary _free_ vessels are attached to the

base of the _rectum_ on one side, which, except in their situation,

seem analogous to the bile-vessels of insects[581].

From the above detailed account of the alimentary canal of the

animals whose internal anatomy we are considering, it appears that

M. Cuvier's observation--that the length and complication of the

intestines indicate a less substantial kind of nutriment--does not

hold universally: thus, in _Necrophorus_ and _Silpha_, _carnivorous_

insects, the intestinal canal in its length and convolutions exceeds

those of most _herbivorous_ ones, and in _Cassida viridis_ and

some others of the _latter_ tribe are not longer than those of the

_predaceous_ beetles. In _herbivorous larvæ_ also, in general, the

length of the alimentary canal does not exceed that of the body, but

in those of some _flesh_-flies (_Musca vomitoria_) it very greatly

exceeds it[582]. So true is the observation--that there is no general

rule without exceptions.

An Introduction to Entomology: Vol. 4 or Elements of the Natural History of the Insects · 第 8 / 50 段