CHAPTER VI

AQUATIC INSECT LARVAE

In this chapter we shall deal with a few aquatic insect larvae. Of

these, some are aquatic also in the perfect condition, while others

emerge from the pupa stage as aërial insects. It requires no great

amount of care to keep these creatures, and some hints on this subject

and on collecting are given in the first chapter.

The larva of Dytiscus is abundant during the greater part of the year,

and is almost sure to be met with by the collector, who will find it

an extremely interesting object for examination and study. No other

creatures should be put in the same bottle with these larvae; and if

there are several of them in one bottle, it is a good plan to put in

plenty of pondweed, which will often keep them from attacking each

other.

When full grown, the Dytiscus larva may attain a length of two inches

or rather more. Its colour is dingy brown, and its aspect forbidding

enough to justify the uncomplimentary names that have been bestowed

upon it--Water-devil and Water-tiger. It certainly rivals the tiger in

fierceness, and its method of stealing up to its prey and attacking it

from behind led Swammerdam to call it the Sicarius or Assassin Worm.

One must not imagine that Swammerdam was ignorant of its nature; ‘worm’

with him was a general term for any larval form. Indeed, he says,

‘It is extremely probable that some peculiar species of the Water

Beetle proceeds from this worm, when, having remained in the water a

sufficient time, it betakes itself to the land to undergo its mutation;

but this is mere conjecture.’ What was conjecture for him is fact for

us.

Now let us put our larva into a small tube, and examine it more

closely. The head is large and joined to the first segment of the

thorax by a distinct neck. There are twelve small eyes, six on each

side, a pair of antennae, two pairs of palps, and a large pair of

sickle-shaped mandibles, which Swammerdam calls ‘teeth,’ and says that

‘it is perhaps to contain the muscles such teeth require that Nature

has made the head so large.’ Behind the head come eleven segments, of

which the first and last are the longest. They gradually increase in

width till the sixth, the rest again decreasing, till the eleventh ends

in a blunt point, from which diverge two appendages, thus [image],

thickly fringed on both sides with hair, as are the tenth and eleventh

segments.

There are six legs, one pair to each of the first three segments.

These also carry fringes of hair, thus increasing their power as

swimming organs; and, in addition, they bear numerous spines, and end

in strong double claws, which must be of service in climbing over

aquatic vegetation, and may assist in holding a struggling victim or in

striking it down, so as to bring it within reach of the mandibles.

Spiracles will be found--seven on each side. These do not, however, in

the larval condition, serve as breathing organs, though they fulfil

their proper office in the pupa. The air-tubes of the larva open at the

extremity of the last segment. When the larva wants to breathe it comes

to the surface without an effort, for it is lighter than the water it

displaces. The tail rises above the surface, and a fresh supply of air

is taken in. When the larva wishes to descend, a stroke of the tail

sends it downwards, and as it reaches the bottom of the tube it will

cling with its claws to any weed we may have put in with it, or hold on

with them to the glass itself.

The chief interest of this animal lies in its mandibles, and the method

in which they are employed. It was formerly believed that the mouth of

this larva was closed, so that it could not take solid food, and that

it lived entirely on the juices of its prey, which it sucked up through

its hollow mandibles.

Swammerdam says of this larva, ‘When about to eat he seizes with the

two teeth (mandibles) the little creatures that come in his way, and

pierces their body with the sharp crooked points. The teeth being

perforated from the points to the roots, he in a surprising manner

sucks through them into his mouth the blood of the unfortunate captive.

This may be easily seen, especially when the blood of his prey is of a

red colour, as the teeth are transparent.’

He then describes how he watched one of these larvae feed, and saw the

blood, mixed with air-bubbles, travel up the mandibles. After this he

tells us how, if we have a Dytiscus larva, we may ‘procure ourselves

a very entertaining and surprising sight, by throwing to it a small

earthworm; for let this last move, twine, and otherwise bestir itself

ever so much, the other keeps its hold, and very calmly sucks the blood

of its prisoner.’

We may, however, go to work in another fashion. We may dissect out the

mandibles from a dead larva and pass a fine hair into the slit near the

point, and it will come out at the orifice near the base. It is through

this orifice that the nutritive juices of the prey are drawn into the

true mouth. This practical proof that the mandibles are pierced is by

no means so difficult as one might suppose.

De Geer[57] seems to have been the first to suggest that there must

be some kind of true mouth, and in support of his suggestion tells us

that he saw this larva eating up the solid parts of a Water Woodlouse

(_cloporte_), after having sucked up its juices. More than this,

he places the mouth in what has proved to be the true position, though

he did not solve the mystery as to why it is kept so firmly closed.

This was done by Mr. Burgess, an American naturalist, from whose

paper[58] the following particulars are condensed:--

‘Authors have described this creature as mouthless; and if we examine

the slit where we should expect the mouth to be, we find that this slit

ends in a perfectly closed seam. The methods of microscopical research

were brought into play, and a longitudinal section of the head cut and

mounted. This showed that the upper and lower lips were locked together

by a peculiar joint--the upper coming over and locking into the under

lip (Fig. 75).’

We may get some idea of this mouth-lock by placing the fingers of the

right hand over those of the left, and then bending them.

Mr. Burgess concludes his paper thus: ‘We find that the Water-tiger,

far from being mouthless, as ordinarily assumed, has in fact a

very wide mouth, though its lips are closely locked together by a

dove-tailed grooved joint developed for this purpose. Whether this

joint can be unlocked by the animal itself is another question, which

I cannot answer, though De Geer’s observation above quoted makes this

probable. It is, at all events, easy to open the mouth by manipulation

with a pair of forceps.’

[Illustration: FIG. 75.--Mouth-lock. _m_, mouth ×

125. (After Burgess.)]

Professor Miall[59] has verified Burgess’s observations, and carried

them a step further. He found by actual experiment that ‘the mouth-lock

acted automatically, opening when the mandibles opened, and closing

when they closed.’

Both these authorities stand very high. Yet, with all respect to them,

it will be well to test these statements before accepting them.

Something of this mouth-lock may be seen in any well-prepared slide

of a Dytiscus larva. If we hold the slide up to the light and examine

with a power of 10, we shall see a dark line--in some cases two nearly

parallel thinner lines--running from the base of one mandible to the

base of the other. The dark line is the closed mouth-lock. The two

nearly parallel thinner lines are the edges of the lips drawn asunder

in preparing the specimen or by the pressure of the cover-glass. If we

get to see this much, we shall have advanced one step.

[Illustration: FIG. 76.--Dytiscus Larvae.]

Next we may verify Professor Miall’s experiment, though not quite in

his way, for such section-cutting as he speaks of is beyond our powers.

Larvae as large as possible should be chosen, and killed by dropping

them into boiling water. The mandibles of one should be allowed to

remain closed, and those of the other plugged open with pith or a small

piece of wood--a bit of a match will serve. By putting each in turn

into an excavated slip with water, carefully covering this with a plain

slip, and holding these slips together with an elastic band, we may

examine the larvae as we did the slide.

The result will be practically the same. Where the mandibles are

closed, we shall see the dark line; and where they are open, we shall

see the two thinner ones nearly parallel.

One caution may be necessary. The mandibles bear at the base a

rounded process, which fits into a chitinous cup. It is not difficult

to mistake this for the mouth-lock, with which, however, it is not

connected.

There is still one other method which we may adopt to see the mouth.

The head of one of these larvae may be cut off, dropped into a strong

solution of caustic potash, where it should remain for a day or two.

After washing it well in water, cut it in half lengthways, and turning

either half upon its side, so as to expose the part cut, examine with

the pocket lens.

These experiments are by no means difficult. But if carried out step

by step, it will be easy to understand how the larva can suck out the

juices of its prey, and how it can open its mouth to swallow some of

the solid parts.

The larva does not readily change into a pupa in confinement. If,

however, we wish to rear a beetle, the larva must be plentifully

supplied with food, and removed from a bottle to a flat dish,

where earth can be placed against the side so as to rise above the

water-level. Fig. 77, where a pupa is represented in a bank by the side

of a pond, will give us a hint how to go to work. The time occupied in

pupation will vary according to the temperature of the room--but is

never less than a fortnight. In the open it is probable that the winter

is passed in the pupal condition, the perfect insect emerging in the

spring. Like Land Beetles, it does not assume its dark hue for some

days, but its pale skin darkens by degrees.

[Illustration: FIG. 77.--Pupa of Dytiscus.]

The larva of Hydrophilus does not seem to be often taken in this

country. It would make a capital subject for investigation, and the

food-supply could be arranged easily enough. The repetition of the

experiences of Lyonnet, who reared these larvae from the egg, would

be of great interest. He says that he took about thirty larvae from

the brood, and fed them with very small water-snails. These they

devoured in the same way as the larger larvae do. Having seized the

snail with their mandibles, they bent backwards, and supporting it

on their back, which served them for a table, eat it there, without

making any use of their legs to hold their prey. When the supply of

small snails ran short, they did very well with large ones cut up into

pieces, and with tadpoles. If, however, food was not supplied to them,

they fed on each other. But, except when pressed by hunger, they lived

together peaceably enough, and seemed to take pleasure in each other’s

society[60].

The larva of _Limnobia replicata_, a Crane-fly allied to, but

smaller than, the well-known Daddy-longlegs, is another excellent

subject for investigation. It is not very often taken; perhaps because

it is not often looked for. But it is common enough, for all that.

In general appearance these larvae resemble small caterpillars covered

with spines. Some of these are simple and others forked, not much

unlike the letter [image], with a short stem, and the arms slightly

curved. There are no feet, and the last segment carries two pairs of

hooks, one large and the other small. From their position they are

called anal hooks.

The dykes of the Sussex marshes are an excellent hunting-ground.

Probably the channels of water-meadows, or any other shallow standing

water in which aquatic moss grows, would serve the collector’s purpose

quite as well. And such pieces of water abound all over the country.

For taking these larvae the ordinary net and bottle are of little use,

though a few may be captured by sweeping backwards and forwards among

patches of aquatic moss.

There is, however, a far easier and surer method. A good handful of

the moss should be gathered, and put into a shallow vessel half full

of water--a developing-dish answers capitally--and then shaken to and

fro or gently stirred with a small piece of stick. The larvae will curl

into a ring and fall to the bottom, whence they may be picked up and

dropped into a bottle or other receptacle to be taken home. A fair

quantity of moss should be gathered, for this is their favourite food,

and all larvae are greedy feeders.

Other water-plants, however, do not come amiss to them. Just before

these lines were written I was examining a bottle in which some of

these larvae were kept. It contained a few sprays of willow-moss and

some ivy-leaved duckweed, which floated on the surface. One larva on a

spray of moss was reaching upward, and it was distinctly seen to feed

on the duckweed. This must have been from choice, for there was within

reach plenty of what all observers consider to be its natural food.

This, too, might have been more easily obtained; for, to reach the

duckweed, the larva had to hold on to the moss by the anal hooks, and

extend its body in a fashion analogous to that of the caterpillar of a

geometer moth, which will hold on to a branch with its fore-legs and

claspers and maintain the body at an angle of 45°, sometimes for hours

together. I have also seen them feed on hornwort.

The larva of this small Crane-fly is not at all difficult to keep. It

is exceedingly hardy, and will survive a great deal of rough treatment.

In November, 1895, I sent three in a tube--securely packed, as I

thought--to a friend in Yorkshire. A few days afterwards I heard, with

regret, ‘that the bottle was broken in transit, and that the larvae

arrived dead.’ Three days later I was gratified by receiving a letter,

from which the following is quoted: ‘The Limnobia larvae have come to

life again. I put them into water as soon as they arrived, and after

lying motionless for many hours they have begun to creep about and

feed.’

This is excellent testimony to their powers of endurance, but it is

weak in comparison to that which De Geer supplies[61].

He was Marshal of the Court of Sweden, and one November, before leaving

his country house for his official duties at Stockholm, he put four

of these larvae into a vessel of water, and left them to take their

chance. The water froze into a solid mass. When he returned in the

following May he found about half the water thawed, and two of the

larvae dead. The others, though they had been enclosed in ice all the

winter, were lively and in good condition. He put them into another

vessel with fresh water and some aquatic moss, and at once they began

to move about and commenced to feed. Both pupated by the fifteenth of

the month, and the perfect fly emerged after six days in the pupal

stage.

[Illustration: FIG. 78.--Larva of _Limnobia

replicata_.]

The following description of this larva is principally condensed from

De Geer, whence the figures are also taken. The body is long and

cylindrical, and divided into eleven segments, of which the first and

largest is sub-triangular. The second and third segments are shorter

than the rest.

The head (_t_) is very small and completely retractile within

the first segment, the anterior margin of which completely closes

the orifice, so that, in this condition, the creature appears to be

headless. The body is covered with spines, some simple and others

branched. On the first three segments there are only simple spines;

but from the fourth to the tenth segment inclusive there are also on

each segment two forked spines--that is, fourteen in all. On the last

segment the spines are simple, and here are also four chitinous hooks,

one pair much larger than the other. These simple spines carry a white

vessel, which extends throughout their whole length; but in the forked

spines there are two such vessels placed side by side in the stem, and

diverging one to each branch.

He comes to the conclusion that these spines are probably the breathing

apparatus of the larva, for they are similar to those which he observed

in an aquatic caterpillar. Walker[62] calls these spines ‘long

filamentous processes, which appear to be internally supplied with

air-tubes,’ but he does not seem to have taken the trouble to break up

a specimen, or he would have been in no doubt as to their real nature.

This is shown by the fact that the larva never comes to the surface to

take in a supply of air, but contents itself with the oxygen dissolved

in the water.

[Illustration:

FIG. 79.--Forked spine of Limnobia, enlarged; the dark

lines show air-tubes.]

The pupa is quite as remarkable as the larva, though the breathing

apparatus does not assume the form of spines, but consists of two

‘trumpets,’ one on each side of the head, as is the case with the

pupae of gnats, using that term in a wide sense. The colour is a

greenish-brown, dotted with black. The abdomen is capable of a good

deal of motion from side to side; and by this means the pupa can raise

itself to the surface of the water to take in a supply of air.

De Geer remarked that when the pupa rose for this purpose it lay with

its body horizontal, having the lips of the trumpets a little above the

surface. It appeared not to like being placed on its back, because in

that position the trumpets cannot be raised above the surface. When he

tried the experiment of putting the pupa back downwards, it wriggled

over by bending the abdomen.

[Illustration: FIG. 80.--Pupa case of Limnobia.

(From a photograph taken at the Yorkshire College, Leeds.)]

On the abdomen there are several chitinous hooks, which serve in some

sort as substitutes for limbs. By their means the pupa can moor itself

to the stems of aquatic plants; and this is necessary, since its

specific gravity being less than that of the water it would be always

at the surface, if it had no such means of anchorage. And of course,

at the top of the water, it would be exposed to the danger of being

snapped up by birds.

De Geer’s specimen passed six days in the pupal state, and then emerged

as a perfect Crane-fly. My specimens did not emerge till after ten and

eleven days of pupahood, which seems strange, as they were plentifully

supplied with food in their larval stage.

The fly is a little more than half an inch long, and may be

distinguished from the common Daddy-longlegs by the character of the

wings, which are folded somewhat like those of a wasp, but with this

difference: that the wings of this fly are folded outward, while those

of the wasp are folded inwards. When the insect wishes to fly, it opens

the fold so that the whole wing presents a plane surface, but the fold

reappears directly the Crane-fly ceases its flight (Frontispiece).

[Illustration: FIG. 81.--Fore-wing of Bee, showing

marginal fold (× 7).]

De Geer’s allusion to the wing of the wasp might have been extended

to most of the Hymenoptera, as we may see by examining the fore and

hind wings of a bee or a sawfly. Dr. Sharp[63] says, ‘The wings [of

the Hymenoptera] are remarkable for the beautiful manner in which the

hinder one is united to the anterior one, so that the two act in flight

as a single organ. The hind wing is furnished with a series of hooks,

and the hind margin of the front wing is curled over so that the hooks

catch on to it. In some of the parasitic forms the wings ... have no

hooks. The powers of flight, in these cases, are probably but small.’

If we were taking our subjects in consecutive order, the larva of

Ptychoptera would properly come here, as being that of a Crane-fly. But

since it will be convenient to examine another larva which resemble

Limnobia in its breathing apparatus, we will take next the larva of

_Parap´onyx stratiota´ta_, one of the China Marks, for it is

extremely interesting and by no means hard to come by.

The China Marks are small moths, with white wings bearing dark

markings, which have been supposed to resemble Chinese characters.

Their larvae are aquatic in varying degree--that is, some breathe air

in the usual way, by means of spiracles; while others, by means of

gills, breathe the oxygen dissolved in the water.

Many collectors have, no doubt, taken these larvae, and cast them away

in the belief that they were caddis-worms. Such was the experience of

the Rev. Gregory Bateman, the author of _Fresh-water Aquaria_,

who says (p. 259): ‘While hunting for fresh-water animals, one not

seldom comes across an insect wrapped up in two or more green leaves,

or pieces of leaves, of some aquatic plant. The leaves and the animal

have somewhat the appearance of a caddis-worm in its case; in fact, for

a time, before I knew what it was, I mistook it (and I daresay others

have done so also) for a caddis-worm.’

The cases are usually, but not invariably, made from the food-plant

of the insect. Mr. Bateman has noted that these larvae ‘do not

always confine themselves to the same weed, either for food or for

building material.’ This has also been my experience. A larva of the

Brown China Mark, recently taken on the Norfolk Broads--an excellent

collecting ground for aquatic larvae--was put into a tube. The case

had been damaged, and the only vegetation in the tube was a spray of

bladderwort. On examining the tube, after some days, I failed to find

the larva. The reason was evident on removing the cork, a small part

of which had been gnawed away to procure material for the repair of

the larval case, which was affixed to the under side. The larva was

dead and too much decayed to be put into pickle, a circumstance I much

regret, as I should like to have preserved the larva in such a strange

dwelling. As it is, I have only been able to keep the house without its

tenant.

Pondweed is the usual home of the larva of the Brown China Mark, and

from the leaves of this plant the first larval case is generally

fashioned. This was the species upon which Réaumur made his interesting

observations, most of which have been confirmed by succeeding

observers. In well-grown larvae the contrivance by which the animal

is protected from contact with the water in which it lives should be

noted, as it may be easily, with the hand lens. The skin is thickly set

with tiny protuberances between which the water cannot penetrate, the

surface film stretching from tip to tip of these prominences, just as

it does over the hairs that cover the body of a water-spider.

De Geer[64] describes an aquatic larva of one of the China Marks

(_Paraponyx stratiotata_), which has its breathing apparatus

fashioned on a similar plan to that of Limnobia, though there is some

difference in the details. He found his specimens on the leaves of the

Water Soldier, and his interesting account recalls the fact to memory

that this remarkable plant was at one time called the Marsh Aloe--an

exceedingly appropriate name.

He describes the filaments on the body of the larva, and concluded

that they were probably breathing-organs, because of the dark-coloured

vessels within them. These he traced, as we will presently do, to their

union in the stem of the gill, and thence to the air-vessels running

down each side of the body of the larva. He fed them on leaves of the

Water Soldier, and kept them through the winter. In the following June

he found them preparing to undergo their transformation into the pupal

stage, and at the end of the month the moths came out. He was gratified

by seeing the congress of these insects. The females deposited their

eggs on the floating vegetation and on the sides of his aquarium, a

little below the surface of the water, and in about eight days the

young larvae were seen.

[Illustration: FIG. 82.--Larva of _Paraponyx

stratiotata_ (enlarged).]

These larvae must be very abundant, though they do not seem to be often

taken by collectors. In describing an allied (American) species, which

is found on Vallisneria and pondweed, Mr. Hart says[65], ‘They feed

at first exposed on the leaf, but later two or even three leaves are

loosely webbed together, face to face, by each larva, between which it

remains concealed while feeding. They are, therefore, hard to discover

unless their hiding-places are broken up by seining, or the like, when

the larvae may be seen swimming about.’ This is, no doubt, the reason

why these larvae are not more often taken. Anything like a seine net is

of course out of the question for us; but masses of vegetation may be

readily broken up by vigorously working the bottle and net backwards

and forwards amongst them. Specimens I have seen were taken among

duckweed; and Mr. Hart mentions one instance of part of the larval case

being constructed of ivy-leaved duckweed, ‘which was abundant there at

that time.’

Now let us bring our lens to bear, so that we may make out the external

structure, and recognize the similarity of the breathing-organs of this

Moth-larva to those of the Crane-fly larva already treated of (p. 168).

In order to make out the scheme of the gills, which is somewhat

complicated, one should first of all distinguish the spiracles,

remembering that they are not functional. And it is best to begin with

those on the middle segments of the body. They may be detected as

little dark spots, sometimes enclosed in a ring. The head, the first

segment of the thorax, and the last segment of the body, bear no gills;

the second segment of the thorax has but two pairs on each side; and

there is but a single gill on each side of the ninth segment of the

body. On the other (nine) body-segments there are the full number

of five gills on each side, arranged two above, and three below the

spiracle. The upper pair are called supra-stigmals, or gills which lie

_above_ the spiracles; the lower pair are called infra-stigmals,

or gills which lie _below_ the spiracles; and the single one, the

lowest, is known as the pedal or foot gill. These technicalities need

not give us any trouble here, in our examination of the larva; nor do

they present any real difficulty. But it is worth while to master the

arrangement as soon as we get hold of one of these larvae, and then we

shall be able to take up and understand technical descriptions of this

aquatic caterpillar and its allies, in so far, at least, as they refer

to the breathing apparatus.

The gills differ in their character: some few are simple, while most of

them are more or less branched. In Limnobia the branching of the gills

is into a simple fork; in Paraponyx this kind of division also occurs,

and in others most of the gill branches are also given off from the

main stem below one of the branches of the fork.

In Fig. 84 we have a representation of one of these branched gills.

It will not be difficult for us to make out the details as there

shown. But the vessels that run down into the filaments, constituting

them breathing-organs, are smaller than those of Limnobia, and will

consequently require a little more care and patience before we can

distinguish them.

[Illustration:

+---------------+

| GILL GILL |

| SPIRACLE |

| GILL GILL |

| GILL |

+---------------+

FIG. 83.--Diagram of segment of Paraponyx, showing

arrangements of tracheal gills.]

[Illustration:

FIG. 84.--Gill of Paraponyx larva. _a_, _b_,

stem; _c_, _d_, _e_, _f_, branches;

_g_, attachment of the air-vessel of the gill to the main

tracheae of the body. (After De Geer.)]

One would think that, with such an array of gills, this larva ought

to be in good case for its air-supply. It may, perhaps, be doubted

whether this is so. At any rate, the creature adopts the same plan as

the larva of Chironomus, which has no gills at all, for driving away

from its case water that has parted with its oxygen. Water charged with

oxygen pours into the case, and so the air-supply is renewed. This plan

is nothing more than keeping the fore-part of the body in undulating

motion, the tail in both the larvae serving as a point of attachment.

One or two that I have kept made their cases against the side of the

bottle, and so afforded an excellent opportunity of seeing them in this

motion. The Tanypus larva does the same thing. Against the side of one

of my small aquaria a Tanypus larva and a Chironomus larva have both

made tubes; and as I look up from writing these lines I can see them

both hard at this work.

The larva of the Alder-fly (_Si´alis luta´rius_) is also furnished

with tracheal gills, seven on each side. So little is known of the

life-histories of common insects that it may be profitable to introduce

the account of an observer who watched the deposition of the eggs and

the emergence of the young larvae:

‘On April 25 I found, on the rushes round the margin of a small pond,

a great many patches of eggs, and shortly after observed many of the

_Sialis lutarius_ depositing them.

‘They form large patches of from two to three inches in length,

generally encircling the whole rush near the top, but sometimes

deposited on one side only, and extended to about a line in breadth.

‘I counted 100 in a square line, so that each batch may be fairly

considered to contain from 2,000 to 3,000 eggs; the greater portion of

which must consequently perish either in the egg or larva state; as,

common as the insect is, and widely distributed throughout the country,

we should be perfectly overwhelmed with the swarms of the perfect

insect if such were permitted, when it is considered that round this

one small pond there could not have been less than 100 patches of them.

‘The eggs are of a very singular form, and placed in a slanting

position.

‘The females, while depositing them, appeared perfectly motionless on

the rush, and varied considerably in size, being from five lines to

nearly double that in length. Some parts of the patches of eggs are of

a much lighter colour than the rest.

‘On May 3 I found many of the eggs hatching, the little larvae tumbling

about in great numbers, with their bodies erected like [the larvae of]

the _Staphylinidae_.

‘On putting them into water they swam about with the greatest activity,

wriggling and undulating their bodies about much like a serpent or the

tadpoles, and working their legs at the same time[66].’

The author draws attention to the disproportionately large head of the

larvae, which, however, he did not describe, as he had ‘brought some of

them alive, and some eggs for exhibition.’

Sialis larvae occur in most ponds with muddy bottoms. They may be taken

by scooping up some of the mud in a long-handled spoon--a most useful

instrument for the collector--and washing it, or by throwing in the

drag, and bringing to land a mass of water-weed, roots and all. A few

may generally be detected near the roots. They may be picked up with a

small pair of forceps, or with a brush, and dropped into a bottle; or,

better still, into separate tubes; for they are fierce and voracious,

and, failing other food, by no means indisposed to prey on each other.

Their general appearance, and especially their powerful mandibles, give

them some resemblance to the larvae of a water beetle, for which a

celebrated naturalist not unnaturally took them, when he began to study

them. And this would seem to be the opinion of some mounters, for I

have a slide of the mouth parts of this larvae, labelled ‘Mouth parts

of the larvae of a water beetle.’ It was not till I had broken up a

good many Sialis larvae that I found out what the slide really was.

These larvae may be kept alive in small bottles of water, if they

are supplied with food. They will eat Chironomus larvae and those of

Tanypus. Professor Miall has found that they will eat caddis-worms and

May-fly larvae. Probably, no small aquatic creatures that they can

overcome are safe from them.

A larva that is full-fed, and ready to change to become a pupa, will

measure about an inch in length or a little more (Fig. 85). The general

colour is brownish, with dark markings. The legs are powerful, and our

lens will show us that they end in two strong curved claws. From each

of the first seven segments of the abdomen are given off a pair of

jointed tracheal gills or breathing-organs, which are directed upwards

and backwards when the larva is at rest--a rare occurrence--but which

wave to and fro in the water when the creature is swimming.

From this fact has arisen the statement found in most books that the

larva uses these gills not only for respiration, but for locomotion.

Professor Miall has come to a contrary conclusion, and, as he has

kindly informed me, is confirmed in his opinion by the weakness of the

muscles.

[Illustration:

FIG. 85.--Larva of Sialis (enlarged).]

It will be well to make repeated observations till we are satisfied

on the subject. When these larvae are kept, the conditions necessary

to provide them with food and to keep the water aërated by means of

growing vegetation are unfavourable to close observation. It will,

therefore, be necessary to remove one or more of these larvae to a

bottle in which there is nothing but pure water.

The work is now rendered much easier. There is nothing to obstruct. As

soon as the larvae reach the bottom they will walk round and round,

giving us a good opportunity of watching them. In swimming--which may

be backwards as well as forwards--the abdomen is waved from side to

side. To see the backward motion one need only put a dipping-tube or a

pencil, or the like, in front of the larva, so as to bar its progress.

The creature will retreat a step or two, and then, with a flourish of

the abdomen, dart back through the water. The larva will sometimes wave

the abdomen up and down, just as one may see a Chironomus larva do when

it has affixed its dwelling to the side of the glass, and this motion

probably assists the process of respiration.

When the larvae have been watched under the conditions above described,

I have never been able to detect independent motion of the gills. But

it is better that every one should observe for himself, and draw his

own conclusions from what he sees.

Now let us examine a specimen more closely with the lens, or under the

dissecting microscope. The mouth parts may be broken up separately, or

a little careful manipulation will enable us to see the chief features

without injuring the specimen. The head is strong and massive, and

the group of ocelli, or simple eyes, may be clearly made out. The

antennae bear a small pencil of hairs, no doubt sensory in function,

at the extremity, but careful management of the light will be required

to distinguish them. The mandibles are extremely business-like

instruments, and each bears two strong teeth on the inner side. Next

come the maxillae, with their palps, each of which has an appendage,

while each maxilla carries three strong spines. The labium, with its

palps, and the mentum, with its saw-like notchings, may be plainly seen.

The three segments of the thorax offer no difficulty. The legs are

worth more than a cursory examination from their apparatus of spines

and double fringe of hairs. Nine body-segments succeed to the thorax,

and behind these is a long tail-like organ, which some authors consider

represents a tenth segment.

[Illustration:

_h_ _t_ 1 2 3 4 5 6 7 8 9 tail

-- ----- -- -- -- -- -- -- -- -- -- ------

| | | | | | | |

FIG. 86.--Diagram of Sialis larva, showing arrangement

of gills (represented by vertical lines). _h_, head;

_t_, thorax; 1–9, segments of abdomen.]

The gills are seven on each side, and are given off from the spaces

in front of the first seven segments of the abdomen. Each gill is

five-jointed--an unusual arrangement, for the gills of the larvae of

Limnobia and Gyrinus are without joints. With the half-inch Leitz the

branching tracheal tube in the gill may be seen, as well as the double

fringe of hairs and the long hairs at the extremity. The tail-like

organ, though without joints, bears a close resemblance to the gills.

It has two tracheal tubes running through it, and it is fringed on both

sides with hair. Indeed, Professor Miall, F.R.S., compares it to ‘two

ordinary tracheal gills completely fused together.’ The first glance

will convince the observer that the comparison is just.

[Illustration: FIG. 87.--Pupa of Sialis.]

The pupa (Fig. 87) need not detain us, for the larva undergoes its

transformation in the ground, not in the water, where it could be

watched. But it is interesting to notice that the legs and wings are

enclosed in separate cases, and that the segments of the abdomen bear

spines. These spines are extremely serviceable to the pupa when making

its way out of its cell to emerge as a perfect insect, which is well

known, especially to fishermen, as the Alder-fly. It may be found near

streams, and rarely uses its wings.

_Ptychoptera paludosa_ is a small Crane-fly, with an aquatic larva

which will repay observation. It is one of the group generally called

‘rat-tailed maggots,’ from the peculiar character of the breathing

apparatus, which consists of a retractile tube at the end of the

abdomen. It is, I believe, better known to some dealers than the larva

of the Drone-fly, the rat-tailed maggot of Réaumur. A few months ago I

wanted some Drone-fly larvae, and asked a dealer to supply me. When the

larvae arrived and were turned out for examination, they proved to be

Ptychoptera larvae--which I did not want. I naturally wrote to point

out the mistake; and was told, in reply, that the larvae sent were the

only ‘rat-tails’ known to my correspondent.

This larva is a mud-dweller, and is best captured by scooping up

surface mud near the banks of pools and ditches, just where the water

shallows on to the shore. This should be washed in a small dish or

saucer, so as to carry away the mud and leave the larvae wriggling

on the bottom. They may be picked up with a brush and dropped into a

bottle for transport home.

There is not the slightest difficulty about keeping them for

observation. A bottle of the capacity of six or eight fluid ounces

will make a good aquarium for a dozen or even twenty. The bottom should

be covered to the depth of about an inch with mud fairly rich in

organic matter. My own plan has been to use the accumulation from the

bottom of a large aquarium. In this the larvae will bury the body, and

feed, the tail protruding and thrust up to the surface of the water, of

which there should be about two inches above the mud.

This is a liberal allowance of space. A couple of these larvae lived

with me for some months in a glass capsule two inches in diameter and

three-quarters of an inch in height. The mud at the bottom and the

water covering it together measured about half an inch. Both pupated,

and in due time from the pupa cases a perfect insect came out.

But that larvae may pupate, they require to be well fed. How shall

we know when the bulk of the nourishment has been extracted from the

mud? From the castings of the larvae; and these, though of a different

shape, are as easy to be distinguished as the castings of the earthworm

in the garden or those of the lobworm on the seashore. All the mud that

passes through the bodies of the larvae is discharged in the form of

tiny hard, cylindrical pellets; and when the mass consists of these

pellets it should be changed, or the larvae will go short of food. They

will, however, support long fasts.

From Fig. 88 we may get a good idea of the appearance of the larvae

when kept in confinement. The figures are rather less than natural

size, and all the attitudes were sketched from life. One is seen

extended on the bottom; two are partially buried in the mud, with the

breathing-tube protruding. The larva on the mud, and bent into curves,

is just about to rise to the surface; others are shown in the act of

rising, while one has its breathing-tube raised above the surface, and

another is attached by the breathing-tube to the side of the glass

vessel. The larva with the star-like process at the end of the tail is

that of Odontomyia, a large bee-like fly.

[Illustration: FIG. 88.--Larvae of _Ptychoptera

paludosa_ (from life).]

A larva of good size, like that of Ptychoptera, is especially easy to

examine; and by reason of its transparency the tracheal tubes may be

clearly traced. The under surface of the larva should be first looked

at, and its adaptation for existence in the mud of a pond-bottom will

be evident. The creature is legless, but possesses three pairs of

false legs armed with dark-coloured hooks, and each body-segment bears

a circle of stiff hairs, which enable the larva to travel through

the mud, in the same way that the earthworm moves through the soil.

Moreover, the segments between these circles are pretty thickly set

with hairs.

The tracheal tubes run down on each side of the body, not in a direct

line, for there is a most ingenious arrangement by which contraction

and expansion of the larva, and the protrusion and retraction of

the tail, are provided for. One can easily discern that in most of

the segments the tubes are large, and that these large portions are

connected by smaller tubes, whence others are given off into the body.

These connecting-tubes are loop-like when the larva is of the normal

length, but are straightened out, thus adding to their length, when the

larva is extended.

The opening and closing of these loops may be observed at leisure if

a larva be put in a long excavated slip, with some water, and then

covered with a plain glass slip. The two slips, fastened together with

small elastic bands, should then be laid on the stage of the dissecting

microscope for examination; or they may be held in the hands, and the

movements of the larva watched with the hand lens.

In the posterior segments of the body the tracheal tubes run side by

side, while in the tail itself they are, so to speak, intertwined. When

the tip of the tail pierces the surface-film a fresh supply of air is

taken in.

At the base of the extensile portion are two processes which diverge,

one on each side, at an angle of 45 degrees. These, according to a

German observer, are tracheal gills, and they are absorbed just before

the larva enters the pupal condition.

Réaumur found these larvae plentifully in the Bois de Boulogne, and

gives a figure[67]. He was not, however, successful in rearing the fly.

Lyonnet not only took the larvae and kept them in an aquarium, but

watched their change into the pupal condition, and saw them emerge as

perfect insects. An abstract of this description will probably be of

interest.

[Illustration:

FIG. 89.--_A._ Ptychoptera larva (enlarged).

_B._ Tail, showing air-vessels (still more enlarged).

(After Lyonnet.)]

He tells us that the larvae showed signs of changing into pupae in

June. The change was made without the larvae leaving the water, and

they underwent all their transformations in less than a fortnight.

At the approach of the change the larvae became whiter in colour,

but less transparent. Then they cast their skin, leaving therein the

air-vessels, or rather their external covering. After this last moult

was over, he was surprised to find that the tube which formed the tail

of the larva, and by which it took in a supply of air, though it serves

the same purpose in the pupa, is attached to the thorax, near the top

of the head[68]. Lyonnet appears to have overlooked the fact that there

was a second and shorter tube given off from the thorax, which most

observers consider to be functionless (Fig. 90).

[Illustration: FIG. 90.--Pupa of Ptychoptera. (After

Lyonnet.)]

Strange as is the larva, the pupa is stranger still, and seems even

better adapted for existence in the mud. The hinder part of each

segment of the abdomen is thickened and studded with chitinous

projections. This thickening is more marked, and of greater extent in

each succeeding segment, reaching its greatest development in the last

segment, which is armed with hooks. The body part of each segment bears

rows of smaller spines, so that this pupa should have little or no

difficulty in moving through pretty thick mud.

Several of these Crane-flies have passed through all their stages with

me, and in nearly every case the transformation from pupa to perfect

insect was made in water--in a tube three inches long, with a diameter

of about an inch. The larvae were taken about the middle of September.

My notes show that the first pupated on November 17, and the first fly

came out on November 25.

The long breathing-tube of the pupa was several times purposely

displaced from its position on the surface. The creature was evidently

incommoded, and twisted itself into strong curves; the head was thrown

from side to side till part of the breathing-tube was raised above the

surface and adhered to the side of the glass tube. Nor did the efforts

cease till a considerable portion of the tube was in free communication

with the air. This would seem to show that the air-supply is taken

through the bladders which appear at irregular intervals in the

breathing-tube, and not at the tip, where the keenest observers have

failed to find an opening.

INDEX

Acridiidae, 80.

Alder-fly, larva of, 177;

pupa of, 182.

American Cockroach, 74.

Amphipods, 141;

Rev. T. R. R. Stebbing on, 141.

Aquaria, description of, 20.

Arachnoidea, 96.

_Argyroneta aquatica_, 108;

De Geer on, 109;

nest of, 110.

Arthropods, 27;

divisions of, 28;

description of, 29.

Ascidians, Darwin on, 13.

_Asellus aquaticus_, description of, 153.

Assassin Worm, 158.

Aurivillius, Dr., on Crabs, 150.

Bate and Westwood on Gammarus, 147;

on Talitrus, 151.

Bateman, Rev. G. C., on Hydrophilus, 50;

on Nepa, 91;

on China Marks, 171.

Beakers, 21.

Beetle Mite, 119.

Belt on Blatta, 67.

Black Beetle, 63.

Black-bobs, 64.

Blackwall on Spiders, 101, 102.

_Blatta orientalis_, description of, 63, 66;

Gilbert White on, 64;

Dr. Sharp on, 65;

Belt on, 67;

Sir J. Lubbock on, 68;

anatomy of, 68;

breathing of, 70;

Swammerdam on, 74;

Professor Plateau on, 74.

Book Scorpions, 96.

_Brachelytra_, 59.

Broad-clawed Porcelain Crab, 139.

Brown China Mark, 172.

Brushes, 23.

Bugs, 86.

Burgess, Mr., on larva of Dytiscus, 160.

Butler, Dr., on Spiders, 100.

Butler, Mr. E. A., on Forficula, 79.

Capsules, 21.

_Carcinus maenas_, description of, 136.

Centipedes, 122;

marine, 125.

Cerci, 47.

Chelate, meaning of word, 132 _n._

China Marks, 171;

Rev. G. C. Bateman on, 171;

De Geer on, 172.

Cockroach, 63.

Cocktail Beetle, 57.

Coleoptera, 32.

Collecting, method of, 25.

Corixa, 94;

Graber on, 95;

Sir J. Lubbock on, 95.

Crab, Shore, 136;

Porcelain, 139.

Crane-fly, 165.

Crustacea, 128.

Daddy-longlegs, 103.

Dallas on Ocypus, 61.

Darwin on microscopes, 12;

on Ascidians, 13.

Devil’s Coach Horse, 57.

Dipping-tubes, 23.

Dissecting microscope, 18.

Dissection, mode of, 37.

Diving Spiders, 108.

Dugès on Water Mites, 117.

Dung Beetle, 119.

_Dytiscus marginalis_, 31;

etymology of, 33 _n._;

breaking of shells by, 33;

Sowerby on, 34;

description of, 35;

food of, 36;

anatomy of, 37;

habits of, 41;

Kirby on, 41;

Sir J. Lubbock on, 42;

Professors Lowne and Miall on, 45;

Dr. Sharp on, 47;

abdomen of, 47;

breathing of, 48;

larva of, 157;

Swammerdam on, 158, 159;

Mr. Burgess on, 160.

Earwig, 75.

Edriophthalma, 129.

Elytra, 41.

_Epeira diadema_, description of, 98;

web of, 98;

J. A. Thomson on, 100;

Dr. Butler on, 100;

Blackwall on, 101, 102;

mode of taking its prey, 102;

Hudson on, 103;

feet of, 104;

spinnerets of, 105.

Evans, W., on Sialis, 177.

_Field_, the, quoted, 33, 35.

Forceps, 22.

_Forficula auricularia_, 75;

Kirby and Spence on, 76;

De Geer on, 76;

young of, 76;

forceps of, 77;

anatomy of, 77;

Butler on, 79;

Dr. Sharp on, 79.

Formalin, 24.

Forty-legs, 122.

Fresh-water Shrimp, 142.

_Gamasus coleoptratorum_, 119.

_Gammarus marinus_, 146;

Dr. J. Salter on, 147.

_Gammarus pulex_, 142;

anatomy of, 144.

Geer, De, on Forficula, 76;

on Locusta, 80;

on Water Mites, 116;

on Beetle Mites, 120;

on Lithobius, 123;

on Julus, 126;

on larva of Limnobia, 167;

on Paraponyx, 172.

Geophilus, 124.

_Geophilus crassipes_, 125;

Mr. Pocock on, 125.

Glass block, 22.

Glass box, 22.

Glass slips, 22.

Gosse on Prawns, 133.

Graber on Corixa, 95.

Grasshopper, Great Green, 80.

Great Water Beetle, 49.

Hart, Mr., on Paraponyx, 173.

Harvestmen, 96.

Hemiptera, 86.

Hill, Dr., on Nepa, 90.

Hudson on Spiders, 103.

Hundred-legs, 122.

Hunting Spiders, 98.

Hydrachna, 113.

_Hydrachna globula_, 118 _n._

Hydrophilus, larva of, 164;

Lyonnet on, 164.

_Hydrophilus piceus_, 49;

Bateman on, 50;

legs of, 53;

Simmermacher on, 53;

breathing of, 54;

cocoons of, 54;

Lyonnet on, 54.

Hymenoptera, wings of, 170.

Idotea, 143.

_Idotea pelagica_, 155.

Illinois State Laboratory, mode of collecting in, 25.

‘Insects,’ 27;

divisions of, 32.

Invertebrates, 28.

Isopods, 152.

Julus, 121, 124.

_Julus terrestris_, 126;

De Geer on, 126;

Dr. Sharp on, 126.

Jumping Spiders, 105.

Kew, Mr., on dispersal of shells, 130.

Kirby on Dytiscus, 41;

on Ocypus, 59;

on Forficula, 76;

on Locusta, 83;

on insect noises, 84;

on Salticus, 107.

Knives, 24.

Land Bugs, 86.

Leaping Orthoptera, 79.

Leitz, lenses of, 16.

Lichtenstein on Locusta, 83.

Limnaea broken by Dytiscus, 33.

_Limnobia replicata_, larva of, 165;

De Geer on, 167;

pupa of, 168.

_Lithobius forficatus_, 122;

De Geer on, 123;

Dr. Sharp on, 123.

_Locusta viridissima_, 80;

Dr. Sharp on, 80, 85;

De Geer on, 80, 83;

Westwood on, 81;

Kirby on, 83;

Lichtenstein on, 83;

ear of, 85.

Locustidae, 80.

Lowne, Professor, on Dytiscus, 45.

Lubbock, Sir J., on Dytiscus, 42;

on Blatta, 68;

on Corixa, 95;

on Opossum Shrimp, 135.

Lyonnet on larva of Hydrophilus, 164;

on Ptychoptera, 186.

Magnification, power of, 15 _n._

Mainland, Mr. G. E., on Water Mites, 118.

Malacostraca, 128;

Rev. T. R. R. Stebbing on, 128.

Margined Water Beetle, 31.

Masking Crabs, 150.

_Melicerta janus_, 150.

Miall, Professor, on Dytiscus, 45;

on Sialis larvae, 179, 181.

Microscopes, use of, 11;

description of, 15.

Millepedes, 121, 125.

Mites, description of, 112.

Model, a calico, 30.

Myriapods, 96, 120.

Mysis, 135.

_Nature Notes_ on Millepedes, 121.

Needles, 23.

_Nepa cinerea_, 86;

mode of keeping, 88;

Swammerdam on, 89;

Dr. Hill on, 90;

Rev. G. C. Bateman on, 91;

anatomy of, 91.

Noises made by insects, 84.

_Notonecta glauca_, 93.

_Ocypus olens_, 57;

Kirby on, 59;

as a pet, 59;

Dallas on, 61;

larva of, 61.

Opossum Shrimp, 135;

Sir J. Lubbock on, 135.

_Orchestia littorea_, 151.

Orthoptera, 63.

Ovipositors, 82.

_Palaemon serratus_, 129.

_Palaemonetes varians_, 130.

_Paraponyx stratiotata_, 171;

De Geer on, 172;

Mr. Hart on, 173;

anatomy of, 174.

Peripatus, 30;

Professor Sedgwick on, 31.

_Periplaneta americana_, 74.

Pholcus, 103.

Phylum, definition of, 27.

Planorbis broken by Dytiscus, 33.

Plateau, Professor, on Blatta, 74.

Pocket lens, description of, 13.

Pocock, Mr., on Geophilus, 125.

Podophthalma, 129.

_Porcellana platycheles_, 139.

Prawns, 129;

Gosse on, 133;

Sowerby on, 133.

Ptychoptera, larva of, 182;

pupa of, 187;

Réaumur on, 185;

Lyonnet on, 186.

Quekett Microscopical Club, incident at, 20.

‘Rat-tails,’ 182.

Réaumur on Ptychoptera, 185.

Robertson, Mr., on Talitrus, 151.

Salter, Dr. J., on Gammarus, 147.

_Salticus scenicus_, 105;

Kirby and Spence on, 107;

foot of, 108.

Sand-hopper, 151.

Scorpions, 96.

Sedgwick, Professor, on Peripatus, 31.

Sharp, Dr., on Dytiscus, 47;

on Blatta, 65;

on Forficula, 79;

on Locusta, 80, 85;

on Lithobius, 123;

on Julus, 126;

on wings of Hymenoptera, 170.

Shells broken by Dytiscus, 33;

Mr. Kew on dispersal of, 130.

Shore Crab, 136.

Shore-hopper, 151.

Shrimp, 132.

_Sialis lutarius_, larva of, 177;

W. Evans on, 177;

anatomy of, 180;

pupa of, 182.

Sicarius, 158.

Simmermacher on Hydrophilus, 53.

Sirex, 82.

Sowerby, G. B., on Dytiscus, 34.

Sphaerium, 130.

Sphaeroma, 155.

Spiders, general description of, 96;

Trap-door, 97;

Hunting, 98;

Garden, 98;

Jumping, 105;

Diving, 108.

Stebbing, Rev. T. R. R., on etymology of Dytiscus, 33 _n._;

on Malacostraca, 128;

on meaning of _chelate_ and _sub-chelate_, 132 _n._;

on Amphipods, 141.

Stewart, Professor, incident of, 20.

Stilopyga, 63.

Swammerdam on Blatta, 74;

on Nepa, 89;

on Water Mites, 114;

on Woodlice, 156;

on Dytiscus larva, 158, 159.

Tailed Wasp, 82.

_Talitrus locusta_, 151;

Bate and Westwood on, 151;

Mr. Robertson on, 152.

Tanypus, larva of, 176.

Tegetmeier, Mr. W. B., on destruction of shells, 34.

Thomson, J. A., on Spiders, 100.

Trap-door Spider, 97.

Vertebrates, 28.

Wart-eater, 81.

Water Beetle, Margined, 31;

the Great, 49.

Water Boatman, 93.

Water Bugs, 86.

Water-devil, 157.

Water Mites, 113;

Swammerdam on, 114;

De Geer on, 116;

Dugès on, 117;

Mainland on, 118.

Water Scorpion, 86.

Water-tiger, 157.

Westwood on Locusta, 81.

White, Gilbert, on Blatta, 64.

Wing-cases, 41.

Wireworm, 126.

Wood, Rev. J. G., on lens stand, 15.

Woodlice, 155;

Swammerdam on, 156.

Worms, 29.

Wright, Mr. L., on microscopes, 16.

Zeiss, lenses of, 15.

THE END.

FOOTNOTES:

[1] Darwin, _Descent of Man_ (2nd ed.), p. 159, note 23.

[2] The power of magnification of a lens is the ratio of its focal

distance to 10 inches. Thus a lens of 1 inch focus (or focal distance)

magnifies 10 times (written × 10, or ten diameters); one of ½ in. focal

distance, 20 times, and so on.

[3] _A Popular Handbook to the Microscope_, p. 39.

[4] _Journal of the Quekett Microscopical Club_, v. 148.

[5] _Ponds and Rock Pools_, p. 17.

[6] _Bulletin of the Illinois State Laboratory of Natural

History_, iv. 158.

[7] ‘Dytiscus’ is written of set purpose. It is not, as some people

tell us, a miswriting for Dyticus; but a properly formed diminutive,

from the Greek _dutēs_ = a diver; like _paidiskos_ = a little boy.

Linnaeus consistently calls the genus Dytiscus from 1735 onwards.

Dyticus only dates from Geoffroy’s _Histoire Abrégée des Insectes_,

first published anonymously in 1762. On this question of nomenclature I

am glad to have the support of the Rev. T. R. R. Stebbing, F.R.S., who,

in answer to my inquiries, kindly wrote, ‘Darwin uses “Dytiscus” in the

_Origin of Species_, and I should decidedly recommend its being upheld.’

[8] April 4, 1896.

[9] _Popular History of the Aquarium_, p. 258.

[10] May 2, 1896.

[11] International Science Series, No. lxv.

[12] _Aquatic Insects_, pp. 55, 56.

[13] _Zeitschrift f. wiss. Zoologie_, Bd. xl. S. 481.

[14] _Mémoires du Muséum d’histoire naturelle_, xviii. 454 sqq.

[15] I have purposely given _Blatta_ as the generic name, rather

than _Stilopyga_, which should properly be used, as the former is

only employed in very recent literature.

[16] Miall and Denny, _The Cockroach_, p. 20.

[17] _Cambridge Natural History_, v. 231.

[18] _The Senses of Animals_, p. 44.

[19] _Cambridge Nat. Hist._ v. 223.

[20] _Book of Nature_, p. 94.

[21] This refers to the gizzard. _Echinus_ was used to denote the

third stomach of Ruminants (now called the manyplies), because it was

thought to resemble a hedgehog rolled up.

[22] Miall and Denny, _The Cockroach_, p. 118 (note).

[23] _Introduction to Entomology_, letter xi.

[24] _Proceedings of the Zoological Society_, 1892, p. 586.

[25] _Our Household Insects_, pp. 159–163.

[26] Kirby and Spence, _Introd. to Entomology_, ed. 1870, p. 484.

[27] _Cambridge Natural History_, v. 318.

[28] _The Senses of Animals_, p. 75.

[29] J. Arthur Thomson, _Outlines of Zoology_, p. 288.

[30] _Science for All_, ii. 178.

[31] _British Spiders_, p. 10.

[32] _British Spiders_, p. 359.

[33] _Naturalist in La Plata_, p. 188.

[34] _Mémoires_, vii. p. 304 sqq.

[35] _Book of Nature_, pp. 101, 102.

[36] _Mémoires_, vii. 144, 145.

[37] The specimen was kindly identified for me, by Dr. Trouessart of

Paris, as a nymph of _Hydrachna globula_ (Dugès), and has been

deposited in the British Museum (Natural History).

[38] _Mémoires_, vii. 123–128.

[39] _Cambridge Natural History_, vol. v. ch. ii.

[40] _Nature_, Dec. 12, 1895.

[41] _Mémoires_, vii. 569.

[42] _Crustacea_, p. 7.

[43] _Crustacea_, p. 225.

[44] International Science Series, No. lxxv.

[45] ‘A limb is _chelate_ when it has joints that will act

together like a pair of tongs. Generally this character is produced by

the hinging of the seventh joint a considerable way down on the side

of the sixth. When the seventh joint, or finger, can be folded back

upon the sixth, although the latter is not produced into any thumb-like

process to oppose it, the limb is then said to be _sub-chelate_,

the claw being in that case partial, though often extremely efficient.’

Stebbing, _Crustacea_ (International Science Series, lxxiv), p. 45.

[46] _Popular History of the Aquarium_, p. 223.

[47] Lubbock, _Senses of Animals_ (International Science Series,

lxv.), p. 93.

[48] _Aquarium_ (ed. 1856), pp. 41, 42.

[49] _Crustacea_ (International Science Series, lxxiv), pp. 8, 9.

[50] Bate and Westwood, _British Sessile-eyed Crustacea_, i. 8.

[51] _Trans. Connecticut Academy_ (1882), iv. 274, 275, note.

[52] _Ponds and Rock Pools_, p. 118.

[53] _British Sessile-eyed Crustacea_, i. 21.

[54] _Proceedings Nat. Hist. Soc. Glasgow_, vol. i. pt. ii. n. s.

pp. 130–132.

[55] _British Sessile-eyed Crustacea_, ii. 381.

[56] _Book of Nature_, i. 174.

[57] _Mémoires_, iv. 386.

[58] _Proceedings Boston Society of Natural History_, xxi. 223–228.

[59] _Natural History of Aquatic Insects_, p. 47.

[60] _Mémoires du Museum_, xviii. 442, 443.

[61] _Mémoires_, vi. 352–55.

[62] _Diptera_, iii. 281.

[63] _Cambridge Natural History_, v. 494.

[64] _Mémoires pour servir_, i. 577 sqq.

[65] _Bulletin of the Illinois State Laboratory of Natural

History_, iv. 167.

[66] W. Evans, _Trans. Entomol. Soc._ (London), iv. 261.

[67] _Mémoires pour servir_, t. vi. Plate 31.

[68] _Mémoires du Muséum_, t. xix. pp. 103, 104.

Transcriber’s Notes:

1. Obvious printers’, punctuation and spelling errors have been

corrected silently.

2. Some hyphenated and non-hyphenated versions of the same words have

been retained as in the original.

3. Superscripts are represented using the caret character, e.g. D^r.

or X^{xx}.

4. Italics are shown as _xxx_.

Through a pocket lens · 第 6 / 6 章