CHAPTER I.

Produced by Bryan Ness, Janet Blenkinship and the Online

Distributed Proofreading Team at http://www.pgdp.net (This

book was produced from scanned images of public domain

material from the Google Print project.)

OUR COMMON INSECTS.

[Illustration: AMERICAN SILK WORM (MALE).]

OUR

COMMON INSECTS.

A POPULAR ACCOUNT OF THE INSECTS

OF OUR

Fields, Forests, Gardens and Houses.

Illustrated with 4 Plates and 268 Woodcuts.

BY

A. S. PACKARD, JR.,

Author of "A GUIDE TO THE STUDY OF INSECTS."

SALEM.

NATURALISTS' AGENCY.

BOSTON: Estes & Lauriat. NEW YORK: Dodd & Mead.

1873.

Entered, according to Act of Congress, in the year 1878, by

F. W. PUTNAM & CO.,

in the Office of the Librarian of Congress at Washington.

PRINTED AT

THE SALEM PRESS,

F. W. PUTNAM & CO.,

Proprietors.

DEDICATION.

TO SAMUEL H. SCUDDER.

MY DEAR SCUDDER:--You and I were drawn together many years ago by a

common love for insects and their ways.

I dedicate this little volume of ephemeral essays to you in recognition

of your worth as a man and a scientist, and as a token of warm

friendship.

Yours sincerely,

A. S. PACKARD, JR.

PREFACE.

This little volume mainly consists of a reprint of a series of essays

which appeared in the "American Naturalist" (Vols. i-v, 1867-71). It is

hoped that their perusal may lead to a better acquaintance with the

habits and forms of our more common insects. The introduction was

written expressly for this book, as well as Chapter XIII, "Hints on the

Ancestry of Insects." The scientific reader may be drawn with greater

interest to this chapter than to any other portion of the book. In this

discussion of a perhaps abstruse and difficult theme, his indulgence is

sought for whatever imperfections or deficiencies may appear. Our

systems of classification may at least be tested by the application of

the theory of evolution. The natural system, if we mistake not, is the

genealogy of organized forms; when we can trace the latter, we establish

the former. Considering how much naturalists differ in their views as to

what is a natural classification, it is not strange that a genealogy of

animals or plants seems absurd to many. To another generation of

naturalists it must, perhaps, be left to decide whether to attempt the

one is more unphilosophical than to attempt the other.

Most of the cuts have already appeared in the "Guide to the Study of

Insects" and the "American Naturalist," where their original sources are

given, while a few have been kindly contributed by Prof. A. E. Verrill,

the Boston Society of Natural History, and Prof. C. V. Riley, and three

are original.

SALEM, June, 1873.

OUR COMMON INSECTS.

INTRODUCTORY.

_What is an Insect?_ When we remember that the insects alone comprise

four-fifths of the animal kingdom, and that there are upwards of 200,000

living species, it would seem a hopeless task to define what an insect

is. But a common plan pervades the structure of them all. The bodies of

all insects consist of a succession of rings, or segments, more or less

hardened by the deposition of a chemical substance called chitine; these

rings are arranged in three groups: the head, the thorax, or middle

body, and the abdomen or hind body. In the six-footed insects, such as

the bee, moth, beetle or dragon fly, four of these rings unite early in

embryonic life to form the head; the thorax consists of three, as may be

readily seen on slight examination, and the abdomen is composed either

of ten or eleven rings. The body, then, seems divided or _insected_ into

three regions, whence the name _insect_.

The head is furnished with a pair of antennæ, a pair of jaws

(mandibles), and two pairs of maxillæ, the second and basal pair being

united at their base to form the so-called labium, or under lip. These

four pairs of appendages represent the four rings of the head, to which

they are appended in the order stated above.

A pair of legs is appended to each of the three rings of the thorax;

while the first and second rings each usually carry a pair of wings.

The abdomen contains the ovipositor; sometimes, as in the bees and

wasps, forming a sting. In the spiders (Fig. 1), however, there are no

antennæ, and the second maxillæ, or labium, is wanting. Moreover, there

are four pairs of legs. The centipedes (Fig. 2, a Myriopod) also differ

from the rest of the insects in having an indefinite number of abdominal

rings, each bearing a pair of legs.

[Illustration: 1. Spider (Tegenaria).]

On examining the arrangement of the parts within, we find the nervous

cord, consisting of two chains of swellings, or nerve-knots, resting

upon the floor or under side of the body; and the heart, or dorsal

vessel, situated just under the skin of the back; and in looking at

living caterpillars, such as the cut-worm, and many thin-skinned aquatic

larvæ, we can see this long tubular heart pulsating about as often as

our own heart, and when the insect is held against its will, or is

agitated, the rapidity of the pulsations increases just as with us.

[Illustration: 2. Centipede.]

Insects do not breathe as in the higher animals by taking the air into

the mouth and filling the lungs, but there are a series of holes or

pores along the side of the body, as seen in the grub of the humble bee,

through which the air enters and is conveyed to every part of the body

by an immense number of air tubes. (Fig. 3, air tubes, or tracheæ, in

the caudal appendage of the larva of a dragon fly). These air tubes are

everywhere bathed by the blood, by which the latter becomes oxygenated.

[Illustration: 3. Caudal appendage of larva of Agrion.]

Indeed the structure of an insect is entirely different from that of man

or the quadrupeds, or any other vertebrate animal, and what we call

head, thorax, abdomen, gills, stomach, skin, or lungs, or jaws, are

called so simply for convenience, and not that they are made in the same

way as those parts in the higher animals.

An insect differs from a horse, for example, as much as a modern

printing press differs from the press Franklin used. Both machines are

made of iron, steel, wood, etc., and both print; but the plan of their

structure differs throughout, and some parts are wanting in the simpler

press which are present and absolutely essential in the other. So with

the two sorts of animals; they are built up originally out of

protoplasm, or the original jelly-like germinal matter, which fills the

cells composing their tissues, and nearly the same chemical elements

occur in both, but the mode in which these are combined, the arrangement

of their products: the muscular, nervous and skin tissues, differ in the

two animals. The plan of structure, namely, the form and arrangement of

the body walls, the situation of the appendages to the body, and of the

anatomical systems within, i.e., the nervous, digestive, circulatory,

and respiratory systems, differ in their position in relation to the

walls of the body. Thus while the two sorts of animals reproduce their

kind, eat, drink and sleep, see, hear and smell, they perform these acts

by different kinds of organs, situated sometimes on the most opposite

parts of the body, so that there is no comparison save in the results

which they accomplish; they only agree in being animals, and in having a

common animal nature.

[Illustration: 4. Different forms of jaws.]

[Illustration: 5. Mouth parts of the Larva of a Beetle.]

[Illustration: 6. Maxilla of a Beetle.]

_How Insects Eat._ The jaws of insects (Fig. 4) are horny processes

situated on each side of the mouth. They are variously toothed, so as to

tear the food, and move horizontally instead of up and down as in the

horse. The act of taking the food, especially if the insect be

carnivorous in its habits, is quite complex, as not only the true jaws,

but the accessory jaws (maxillæ, Fig. 5, _a_, upper, b, under side of

the head of a young beetle; _at_, antennæ, _md_, mandible, _mx_,

maxillæ, _mx_[1], labium) and the feelers (palpi) attached to the

maxillæ, and the under lip (labium) are of great service in enabling the

insect to detect its food both by the senses of touch and smell. The

maxillæ are in the fully grown beetle (Fig. 6) divided into three lobes,

the outermost forming the palpus, and the two others forming sharp

teeth, often provided with hairs and minute brushes for cleansing the

adjoining parts; these strong curved teeth are used in seizing the food

and placing it between the grinders, where it is crushed, prepared for

digestion and swallowed. Fig. 7 represents the mouth parts of the humble

bee. (_b_, upper lip; _d_, mandible; _e_, maxilla; _f_, maxillary

palpus; _g_, tongue; _ih_, labium and tabial palpi; _k_, eye.)

[Illustration: 7. Mouth parts of a Humble Bee.]

The alimentary canal passes through the middle of the body, the stomach

forming usually a simple enlargement. Just before the stomach in certain

insects, as the grasshopper, is a gizzard armed with rows of powerful

horny teeth for finely crushing grass.

Insects eat almost incredible quantities of food when young and growing

rapidly. Mr. Trouvelot tells us in the "American Naturalist" that the

food taken by a single American Silk-worm in fifty-six days is equal to

eighty-six thousand times its primitive weight! On the other hand, after

the insect has finished its transformations, it either takes no food at

all, as in the May fly, or merely sips the honey of flowers, as in the

butterfly, while the June beetle and many others like it eat the leaves

of trees, and the tiger and ground beetles feed voraciously on other

insects.

_How Insects Walk._ In man and his allies, the vertebrates, the process

of walking is a most difficult and apparently dangerous feat. To

describe the mechanics of walking, the wonderful adaptation of the

muscles and bones for the performance of this most ordinary action of

life, would require a volume. The process is scarcely less complex in

insects. Lyonnet found 3,993 muscles in a caterpillar, and while a large

proportion belong to the internal organs, over a thousand assist in

locomotion. Hence the muscular power of insects is enormous. A flea will

leap two hundred times its own height, and certain large, solid beetles

will move enormous weights as compared to the bulk of their bodies.

[Illustration: 8. Larva of a beetle (Photuris).]

In walking, as seen in the accompanying figure (Fig. 8), three legs are

thrown forward at a time, two on one side and one on the other.

Flies and many other insects can walk upside down, or on glass, as

easily as on a level surface. A fly's foot, as in most other insects,

consists of five joints (tarsal joints), to the last one of which is

appended a pair of stout claws, beneath which is a flat, soft, fleshy

cushion or pad, split into two (sometimes three) flaps, beset on the

under surface with fine hairs. A part of these hairs are swollen at the

end, which is covered with "an elastic membranous expansion, capable of

close contact with a highly polished surface, from which a minute

quantity of a clear, transparent fluid is emitted when the fly is

actively moving." (T. West.) These hairs are hence called holding, or

tenent, hairs. With the aid of these, but mainly, as Mr. West insists,

by the pressure of the atmosphere, a fly is enabled to adhere to

perfectly smooth surfaces. His studies show the following curious facts.

"That atmospheric pressure, if the area of the flaps be alone

considered, is equal to just one-half the weight of a fly. If the area

covered by the tenent hairs be added, an increase of pressure is gained,

equal to about one-fourth the weight of a fly. This leaves one-fourth to

be accounted for by slight viscidity of the fluid, by the action I have

so often alluded to, which may be called 'grasping,' by molecular

attraction, and, doubtless, by other agents still more subtle, with

which we have at present scarcely any acquaintance."

_How Insects Fly._ Who of us, as remarked by an eminent ornithologist,

can even now explain the long sustained, peculiar flight of the hawk, or

turkey buzzard, as it sails in the air without changing the position of

its wings? and, we would add, the somewhat similar flight of a

butterfly? It is the poetry of motion, and a marvellous exhibition of

grace and ease, combined with a wonderful underlying strength and

lightness of the parts concerned in flight.

Before we give a partial account of the results obtained by the delicate

experiments of Professor Marey on the flight of birds and insects, our

readers should be reminded of the great differences between an insect

and a bird, remembering that the former, is, in brief, a chitinous sac,

so to speak, or rather a series of three such spherical or elliptical

sacs (the head, thorax and abdomen); the outer walls of the body forming

a solid but light crust, to which are attached broad, membranous wings,

the wing being a sort of membranous bag stretched over a framework of

hollow tubes (the tracheæ), so disposed as to give the greatest

lightness and strength to the wing. The wings are moved by powerful

muscles of flight, filling up the cavity of the thorax, just as the

muscles are the largest about the thorax of a bird. Moreover in the

bodies of insects that fly (such as the bee, cockchafer, and dragon

fly), as distinguished from those that creep exclusively, the air tubes

(tracheæ) which ramify into every part of the body, are dilated here and

there, especially in the base of the abdomen, into large sacs, which are

filled with air when the insect is about to take flight, so that the

specific gravity of the body is greatly diminished. Indeed, these air

sacs, dilatable at will by the insect, may be compared to the swimming

bladder of fishes, which enables them to rise and fall at will to

different levels in the sea, thus effecting an immense saving of the

labor of swimming. In the birds, as every body knows who has eaten a

chicken, or attended the dissection of a Thanksgiving turkey, the soft

parts are external, attached to the bony framework comprising the

skeleton, the wing bones being directly connected with the central back

bone; so that while these two sorts of animated flying machines are so

different in structure, they yet act in much the same manner when on the

wing. The difference between them is clearly stated by Marey, some of

whose conclusions we now give almost word for word.

The flight of butterflies and moths differs from that of birds in the

almost vertical direction of the stroke of their wings, and in their

faculty of sailing in the air without making any movements; though

sometimes in the course they pursue they seem to resemble birds in their

flight.

The flight of insects and birds moreover differs in the form of the

trajectory in space; in the inclination of the plane in which the wings

beat; in the role of each of the two alternating (and in an inverse

sense) movements that the wings execute; as also in the facility with

which the air is decomposed during these different movements. As the

wings of a fly are adorned with a brilliant array of colors, we can

follow the trajectory or figure that each wing writes in the air. It is

of the form of a figure of eight (Fig. 9), first discovered by Professor

J. Bell Pettigrew of Edinburgh.

[Illustration: 9. Figure cut by an insect's wing.]

[Illustration: 10. Figure cut by a bird's wing.]

By an ingenious machine, specially devised for the purpose, Professor

Marey found that a bird's wing moves in an ellipse, with a pointed

summit (Fig. 10). The insect beats the air in a distinctly horizontal

plane, but the bird in a vertical plane. The wing of an insect is

impervious to the air; while the bird's wing resists the air only on

its under side. Hence, there are two sorts of effects; in the insect

the up and down strokes are active; in the bird, the lowering of the

wing is the only active period, though the return stroke seems to

sustain the bird, the air acting on the wing. The bird's body is

horizontal when the wing gives a downward stroke; but when the beat is

upward, the bird is placed in an inclined plane like a winged

projectile, and mounts up on the air by means of the inclined surfaces

that it passively offers to the resistance of this fluid.

[Illustration: 11. Trajectory of an insect's wing.]

[Illustration: 12. Trajectory of a bird's wing.]

In an insect, an energetic movement is equally necessary to strike the

air at both beats up and down. In the bird, on the contrary, one active

beat only is necessary, the down beat. It creates at that time all the

motive force that will be dispensed during the entire revolution of the

wing. This difference is due to the difference in form of the wing. The

difference between the two forms of flight is shown by an inspection of

the two accompanying figures (11, 12). An insect's wing is small at the

base and broad at the end. This breadth would be useless near the body,

because at this point the wing does not move swiftly enough to strike

the air effectively. The type of the insectean wing is designed, then,

simply to strike the air. But in the bird the wing plays also a passive

role, _i. e._, it receives the pressure of the air on its under side

when the bird is projected rapidly onward by its acquired swiftness. In

these conditions the whole animal is carried onward in space; all the

points of its wing have the same velocity. The neighboring regions of

the body are useful to press upon the air, which acts as on a paper

kite. The base of the wing also, in the bird, is broad, and provided

with feathers, which form a broad surface, on which the air presses with

a force and method very efficacious in supporting the bird. Fig. 12

gives an idea of this disposition of the wing at the active and passive

time in a bird.

The inner half of the wing is the passive part of the organ, while the

external half, that which strikes the air, is the active part. A fly's

wing makes 330 revolutions in a second, executing consequently 660

simple oscillations; it ought at each time to impress a lateral

deviation of the body of the insect, and destroy the velocity that the

preceding oscillation has given it in a contrary direction. So that by

this hypothesis the insect in its flight only utilizes fifty to one

hundred parts (or one-half) of the resistance that the air furnishes it.

[Illustration: 13. A bird on the wing.]

In the bird (Fig. 13), at the time of lowering the wings, the oblique

plane which strikes the air, in decomposing the resistance, produces a

vertical component which resists the weight of the body, and a

horizontal component which imparts swiftness. The horizontal component

is not lost, but is utilized during the rise of the wing, as in a paper

kite when held in the air against the wind. Thus the bird utilizes

seventy-five out of one hundred parts of the resistance that the air

furnishes. The style of flight of birds is, therefore, theoretically

superior to that of insects. As to the division of the muscular force

between the resistance of the air and the mass of the body of the bird,

we should compare the exertion made in walking on sand, for example, as

compared with walking on marble. This is easy to measure. When a fish

strikes the water with its tail to propel itself forward, it performs a

double task; one part consists in pushing backwards a certain mass of

water with a certain swiftness, and the other in pushing on the body in

spite of the resistance of the surrounding fluid. This last portion of

the task only is utilized. It would be greater if the tail of the fish

encountered a solid object. Almost all the propelling agencies employed

in navigation undergo this loss of labor, which depends on the mobility

of the _point d' appui_. The bird is placed among conditions especially

unfavorable.

_The Senses of Insects._ The eyes of insects are sometimes so large as

to envelop the head like an Elizabethan ruffle, and the creature's head,

as in the common house fly, seems all eyes. And this is almost literally

the case, as the two great staring eyes that almost meet on the top of

the head to form one, are made up of myriads of simple eyes. Each facet

or simple eye is provided with a nerve filament which branches off from

the main optic nerve, so that but one impression of the object perceived

is conveyed to the brain; though it is taught by some that objects

appear not only double but a thousand times multiplied. But we should

remember that with our two eyes we see double only when the brain is

diseased. Besides the large ordinary compound eyes, many insects possess

small, simple eyes, like those of the spider. The great German

anatomist, Johannes Müller, believed that the compound eyes were adapted

for the perception of distant objects, while those nearer are seen by

the simple eyes. But it may be objected to this view that the spiders,

which have only simple eyes, apparently see both near and remote objects

as well as insects.

The sense of touch is diffused all over the body. As in the hairs of the

head and face of man, those of insects are delicate tactile organs; and

on the antennæ and legs (insects depending on this sense rather than

that of sight) these appendages are covered with exquisitely fine

hairs. It is thought by some that the senses of hearing and smell are

lodged in the antennæ, these organs thus combining the sense of feeling

with those of hearing and smelling. And the researches of anatomists

lend much probability to the assertion, since little pits just under the

skin are found, and even sometimes provided with grains of sand in the

so-called ear of the lobster, etc., corresponding to the ear bones of

the higher animals, the pits being connected with nerves leading to the

brain. We have detected similar pits in the under side of the palpi of

the Perla. It seems not improbable that these are organs of smell, and

placed in that part of the appendage nearest the mouth, so as to enable

the insect to select its proper food by its odor. Similar organs exist

on the caudal appendages of a kind of fly (Chrysopila), while the long,

many-jointed caudal filaments of the cockroach are each provided with

nearly a hundred of these little pits, which seem to be so many noses.

Thus Lespès, a Swiss anatomist, in his remarks on the auditory sacs,

which he says are found in the antennæ of nearly all insects, declares

that as we have in insects compound eyes, so we have compound ears. We

might add that in the abdominal appendage of the cockroach we have a

compound nose, while in the feelers of the Perla, and the caudal

appendage of the Chrysopila, the "nose" is simple. We might also refer

here to Siebold's discovery of ears at the base of the abdomen of some,

and in the forelegs of other kinds, of grasshoppers. Thus we need not be

surprised at finding ears and noses scattered, as it were, sometimes

almost wantonly over the bodies of insects (in many worms the eyes are

found all over the body), while in man and his allies, from the monkey

down to the fish, the ears and nose invariably retain the same relative

place in the head.

_How Insects Grow._ When beginning our entomological studies no fact

seemed more astonishing to our boyish mind than the thought that the

little flies and midges were not the sons and daughters of the big

ones. If every farmer and gardener knew this single fact it would be

worth their while. The words _larva_ and _pupa_ will frequently occur in

subsequent pages, and they should be explained. The caterpillar (Fig.

14, _a_) represents the earliest stage or babyhood of the butterfly, and

it is called _larva_, from the Latin, meaning a mask, because it was

thought by the ancients to mask the form of the adult butterfly.

[Illustration: 14. _a_ Larva, _b_ chrysalis of a butterfly.]

When the caterpillar has ended its riotous life, for its appetite almost

transforms its being into the very incarnation of gluttony, it suddenly,

as if repenting of its former life as a _bon vivant_, seeks a solitary

cell or hole where like a hermit it sits and leads apparently about as

useless an existence. But meanwhile strange processes are going on

beneath the skin; and after a few convulsive struggles the back splits

open, and out wriggles the chrysalis, a gorgeous, mummy-like form, its

body adorned with golden and silvery spots. Hence the word chrysalis

(Fig. 14, _b_), from the Greek, meaning golden, while the Latin word

_pupa_, meaning a baby or doll, is indicative of its youth. In this

state it hangs suspended to a twig or other object; while the silk worm,

and others of its kind, previous to moulting, or casting their skins,

spin a silken cocoon, which envelops and protects the chrysalis.

[Illustration: 15. Imago or adult Butterfly.]

At the given time, and after the body of the adult has fully formed

beneath the chrysalis skin, there is another moult, and the butterfly,

with baggy, wet wings, creeps out. The body dries, the skin hardens, the

wings expand, and in a few moments, sometimes an hour, the butterfly

(Fig. 15) proudly sails aloft, the glory and pride of the insect world.

We shall see in the ensuing chapters how varied are the larvæ and pupæ

of insects, and under what different guises insects live in their early

stages.

[Illustration: Larva, pupa, and adult of a Leaf Beetle (Galeruca).]

OUR COMMON INSECTS.

CHAPTER I.

THE HOME OF THE BEES.

The history of the Honey bee, its wonderful instincts, its elaborate

cells and complex economy, have engrossed the attention of the best

observers, even from the time of Virgil, who sang of the Ligurian bee.

The literature of the art of bee-keeping is already very extensive.

Numerous bee journals and manuals of bee-keeping testify to the

importance of this art, while able mathematicians have studied the mode

of formation of the hexagonal cells,[1] and physiologists have

investigated the intricate problems of the mode of generation and

development of the bee itself.

In discussing these difficult questions, we must rise from the study of

the simple to the complex, remembering that--

"All nature widens upward. Evermore

The simpler essence lower lies:

More complex is more perfect--owning more

Discourse, more widely wise."

and not forget to study the humbler allies of the Honey bee. We shall,

in observing the habits and homes of the wild bees, gain a clearer

insight into the mysteries of the hive.

The great family of bees is divided into social and solitary species.

The social kinds live in nests composed of numerous cells in which the

young brood are reared. These cells vary in form from those which are

quite regularly hexagonal, like those of the Hive bee, to those which

are less regularly six-sided, as in the stingless bee of the tropics

(Melipona), until in the Humble bee the cells are isolated and

cylindrical in form.

Before speaking of the wild bees, let us briefly review the life of the

Honey bee. The queen bee having wintered over with many workers, lays

her eggs in the spring, first in the worker, and, at a later period, in

the drone-cells. Early in the summer the workers construct the large,

flask-shaped queen-cells, which are placed on the edge of the comb, and

in these the queen larvæ are fed with rich and choice food. The old

queen deserts the nest, forming a new colony. The new-born queen takes

her marriage flight high in the air with a drone, and on her return

undertakes the management of the hive, and the duty of laying eggs. When

the supply of queens is exhausted, the workers destroy the drones. The

first brood of workers live about six weeks in summer, and then give way

to a new brood. The queens, according to Von Berlepsch, are known to

live five years, and during their whole life lay more than a million

eggs.

In the tropics, the Honey bee is replaced by the Meliponas and Trigonas.

They are minute, stingless bees, which store up honey and live in

colonies often of immense extent. The cells of Melipona are hexagonal,

nearly approaching in regularity those of the Hive bee, while the honey

cells are irregular, being much larger cavities, which hold about

one-half as much honey as a cell of the Humble bee. "Gardner, in his

travels, states that many species of Melipona build in the hollow trunks

of trees, others in banks; some suspend their nests from the branches of

trees, whilst one species constructs its nest of clay, it being of large

size." (F. Smith.)

In a nest of the coal-black Trigona (Trigona carbonaria), from eastern

Australia, Mr. F. Smith, of the British Museum, found from four hundred

to five hundred dead workers, but no females. The combs were arranged

precisely similar to those of the common wasp. The number of honey-pots

which were placed at the foot of the nest was two hundred and fifty. Mr.

Smith inclines to the opinion that the hive of Trigona contains several

prolific females, as the great number of workers can only be thus

explained, and M. Guérin found six females in a nest of the Tawny-footed

Melipona (M. fulvipes).

At home, our nearest ally of the true Honey bee, is the Humble bee

(Bombus), of which over forty species are known to inhabit North

America.

The economy of the Humble bee is thus: the queen awakens in early spring

from her winter's sleep under leaves or moss, or in the last year's

nest, and selects a nesting place, generally in an abandoned nest of a

field-mouse, or beneath a stump or sod, and "immediately," according to

Mr. F. W. Putnam,[2] "collects" a small amount of pollen mixed with

honey, and in this deposits from seven to fourteen eggs, gradually

adding to the pollen mass until the first brood is hatched. She does not

wait, however, for one brood to be hatched before laying the eggs of

another, but, as soon as food enough has been collected, she lays the

eggs for a second. The eggs are laid, in contact with each other, in one

cavity of the mass of pollen, with a part of which they are slightly

covered. They are very soon developed; in fact, the lines are nowhere

distinctly drawn between the egg and the larva, the larva and pupa, and

again between the latter and the imago; a perfect series, showing this

gradual transformation of the young to the imago can be found in almost

every nest.

[Illustration: 15. Cell and Eggs of Bombus.]

"As soon as the larvæ are capable of motion and commence feeding, they

eat the pollen by which they are surrounded, and, gradually separating,

push their way in various directions. Eating as they move, and

increasing in size quite rapidly, they soon make large cavities in the

pollen mass. When they have attained their full size, they spin a silken

wall about them, which is strengthened by the old bees covering it with

a thin layer of wax, which soon becomes hard and tough, thus forming a

cell (Fig. 15, 1, cell containing a larva, on top of which (2) is a

pollen mass containing three eggs). The larvæ now gradually attain the

pupa stage, and remain inactive until their full development. They then

cut their way out, and are ready to assume their duties as workers,

small females, males or queens.

"It is apparent that the irregular disposition of the cells is due to

their being constructed so peculiarly by the larvæ. After the first

brood, composed of workers, has come forth, the queen bee devotes her

time principally to her duties at home, the workers supplying the colony

with honey and pollen. As the queen continues prolific, more workers are

added, and the nest is rapidly enlarged.

"About the middle of summer, eggs are deposited, which produce both

small females and males." ... "All eggs laid after the last of July

produce the large females, or queens, and, the males being still in the

nest, it is presumed that the queens are impregnated at this time, as on

the approach of cold weather all except the queens, of which there are

several in each nest, die."

While the Humble bee in some respects shows much less instinct than the

solitary bees mentioned below, it stands higher in the series, however,

from having workers, as well as males and females, who provide food for

the young. The labors of the Mason bees, and their allies, terminate

after the cell is once constructed and filled with pollen. The eggs are

then left to hatch, and the young care for themselves, though the adult

bee shows greater skill in architecture than the Humble bee. It is thus

throughout nature. Many forms, comparatively low in the scale of life,

astonish us with certain characters or traits, reminding us of beings

much superior, physically and intellectually. The lower forms constantly

reach up and in some way ally themselves with creatures far more highly

organized. Thus the fish-like seal reminds us strikingly of the dog,

both in the form of the head, in its docility and great intelligence

when tamed, and even in its bark and the movements of the head.

[Illustration: 16. Meloë.]

The parasites of the Humble bee are numerous. Such are the species of

Apathus, which so closely resembles the Humble bee itself, that it

requires long study to distinguish it readily. Its habits are not known,

other than that it is found in the nests of its host. It differs from

the Humble bee in having no pollen-basket, showing that its larvæ must

feed on the food stored up by their host, as it does not itself collect

it. The mandibles also are not, like those of Bombus, trowel-shaped for

architectural purposes, but acutely triangular, and are probably not

used in building.

The caterpillars of various moths consume the honey and waxen cells; the

two-winged flies, Volucella and Conops, and the larvæ of what is either

an Anthomyia or Tachina-like fly, and several species of another genus

of flies, Anthrax, together with several beetles, such as the Meloë

(Fig. 16), Stylops (Fig. 17, male; 18_b_, female; _a_, position in the

body of its host), and Antherophagus prey upon them.

[Illustration: 17. Male Stylops.]

The power of boring the most symmetrical tunnels in solid wood reaches

its perfection in the large Virginian Carpenter bee (Xylocopa Virginica,

Fig. 19). This bee is as large as, and some allied exotic species are

often considerably larger than, the Humble bee, but not clothed with

such dense hairs. We have received from Mr. James Angus, of West Farms,

N. Y., a piece of trellis from a grape vine, made of pine wood,

containing the cells and young in various stages of growth, together

with the larvæ and chrysalids of Anthrax sinuosa (Fig. 20), a species of

fly parasitic on the larva. The maggot buries its head in the soft body

of the young bee and feeds on its juices.

Mr. Angus thus writes us regarding its habits, under date of July 19: "I

asked an intelligent and observing carpenter yesterday, if he knew how

long it took the Xylocopa to bore her tunnel. He said he thought she

bored about one-quarter of an inch a day. I don't think myself she

bores more than one-half inch, if she does that. If I mistake not, it

takes her about two days to make her own length at the first start; but

this being across the grain of the wood, may not be so easily done as

the remainder, which runs parallel with it. She always follows the grain

of the wood, with the exception of the entrance, which is about her own

length. The tunnels run from one to one and a half feet in length. They

generally run in opposite directions from the opening, and sometimes

other galleries are run, one directly above the other, using the same

opening. I think they only make new tunnels when old ones are not to be

found, and that the same tunnels are used for many years. Some of the

old tunnels are very wide. I have found parts of them about an inch in

diameter. I think this is caused by rasping off the sides to procure the

necessary material for constructing their cells. The partitions are

composed of wood raspings, and some sticky fluid, probably saliva, to

make them adhere.

[Illustration: 18. Female Stylops.]

[Illustration: 19. Carpenter Bee.]

"The tunnels are sometimes taken possession of by other bees and wasps.

I think when this is the case, the Xylocopa prefers making a new cell,

to cleaning out the dirt and rubbish of the other species. I frequently

find these bees remaining for a long time on the wing close to the

opening, and bobbing their heads against the side, as if fanning air

into the opening. I have seen them thus employed for twenty minutes.

Whether one bee or more makes the tunnel, that is, whether they take

turns in boring, I cannot at present say. In opening the cells (Fig.

21), more than one are generally found, even at this season. About two

weeks ago; I found as many as seven, I think, in one."[3]

The hole is divided by partitions into cells about seven-tenths of an

inch long. These partitions are constructed of the coarse dust or

chippings made by the bee in eating out her cells, for our active little

carpenter is provided with strong cutting jaws, moved by powerful

muscles, and on her legs are stiff brushes of hair for cleaning out the

tunnel as she descends into the heart of the solid wood. She must throw

out the chips she bites off with her powerful mandibles from the sides

of the burrow, by means of her hind legs, passing the load of chips

backwards out of the cell with her fore limbs, which she uses as hands.

[Illustration: 20. Larva and Pupa of Anthrax.]

The partitions are built most elaborately of a single flattened band of

chips, which is rolled up into a coil four layers deep. One side,

forming the bottom of the cell, is concave, being beaten down and

smoothed off by the bee. The other side of the partition, forming the

top of the cell, is flat and rough.

[Illustration: 21. Nest of Carpenter Bee.]

At the time of opening the burrow, July 8th, the cells contained nearly

full-grown larvæ, with some half developed. They were feeding on the

masses of pollen, which were as large as a thick kidney bean, and

occupied nearly half the cell. The larvæ (Fig. 21) resemble those of the

Humble bee, but are slenderer, tapering more rapidly towards each end of

the body.

The habits and structure of the little green Ceratina ally it closely

with Xylocopa. This pretty bee, named Ceratina dupla by Mr. Say, tunnels

out the stems of the elder or blackberry, syringa, or any pithy shrub,

excavating them often to a depth of six or seven inches. She makes the

walls just wide enough to admit her body, and of a depth capable of

holding three or four, often five or six cells (Fig. 22). The finely

built cells, with their delicate silken walls, are cylindrical and

nearly square at each end, though the free end of the last cell is

rounded off. They are four and a half tenths of an inch long, and a

little over one-third as broad. The bee places them at nearly equal

distances apart, the slight interval between them being filled in with

dirt.

[Illustration: 22. Nest of Ceratina.]

Dr. T. W. Harris states that May 15, 1832, one female laid its eggs in

the hollow of an aster stalk. Three perfect insects were disclosed from

it July 28th. The observations of Mr. Angus, who saw some bees making

their cells May 18th, also confirm this account. The history of our

little upholsterer is thus cleared up. Late in the spring she builds her

cells, fills them with pollen, and lays one or more eggs upon each mass.

Thus in about two months the insect completes its transformations;

within this period passing through the egg, the larva and chrysalid

states, and then, as a bee, living a few days more, if a male; or if a

female, living through the winter. Her life thus spans one year.

The larva (Fig. 23) is longer than that of Megachile, and compared with

that of Xylocopa, the different segments are much more convex, giving a

serrate outline to the back of the worm. The pupa, or chrysalis, we have

found in the cells the last of July. It is white, and three-tenths of an

inch long. It differs from that of the Leaf-cutter bee in having four

spines on the end of the body.

[Illustration: 23. Larva of Ceratina.]

[Illustration: 24. Nest of Tailor Bee.]

In none of the wild bees are the cells constructed with more nicety than

those of our little Ceratina. She bores out with her jaws a long deep

well just the size of her body, and then stretches a thin, delicate

cloth of silk drawn tight as a drum-head across each end of her

chambers, which she then fills with a mixture of pollen and honey.

[Illustration: 25. Tailor Bee.]

Her young are not, in this supposed retreat, entirely free from danger.

The most invidious foes enter and attack the brood. Three species of

Ichneumon flies, two of which belong to the Chalcid family, lay their

eggs within the body of the larva, and emerge from the dried larva and

pupa skins of the bee, often in great numbers. The smallest parasite,

belonging to the genus Anthophorabia, so called from being first known

as a parasite on another bee (Anthophora), is a minute species found

also abundantly in the tight cells of the Leaf-cutter bee.

The interesting habits of the Leaf-cutting, or Tailor bee (Megachile),

have always attracted attention. This bee is a stout, thick-bodied

insect, with a large, square head, stout, sharp, scissors-like jaws, and

with a thick mass of stout, dense hairs on the under side of the tail

for carrying pollen, as she is not provided with the pollen-basket of

the Honey and Humble bees.

The Megachile lays its eggs in burrows in the stems of the elder (Fig.

24), which we have received from Mr. James Angus; we have also found

them in the hollows of the locust tree. Mr. F. W. Putnam thus speaks of

the economy of M. centuncularis, our most common species. "My attention

was first called, on the 26th of June, to a female busily engaged in

bringing pieces of leaf to her cells, which she was building under a

board, on the roof of the piazza, directly under my window. Nearly the

whole morning was occupied by the bee in bringing pieces of leaf from a

rose bush growing about ten yards from her cells, returning at intervals

of a half minute to a minute with the pieces, which she carried in such

a manner as not to impede her steps when she alighted near her hole."

When the Leaf-cutter bee wishes to cut out a piece of a leaf (Fig. 25)

she alights upon the leaf, and in a few seconds swiftly runs her

scissors-like jaws around through it, bearing off the piece in her hind

legs. "About noon she had probably completed the cell, upon which she

had been engaged, as, during the afternoon, she was occupied in bringing

pollen, preparatory to laying her single egg in the cell. For about

twenty days the bee continued at work, building new cells and supplying

them with pollen.... On the 28th of July, upon removing the board, it

was found that the bee had made thirty cells, arranged in nine rows of

unequal length, some being slightly curved to adapt them to the space

under the board. The longest row contained six cells, and was two and,

three-quarters inches in length; the whole leaf structure being equal to

a length of fifteen inches. Upon making an estimate of the pieces of

leaf in this structure, it was ascertained that there must have been at

least a thousand pieces used. In addition to the labor of making the

cells, this bee, unassisted in all her duties, had to collect the

requisite amount of pollen (and honey?) for each cell, and lay her eggs

therein, when completed. Upon carefully cutting out a portion of one of

the cells, a full-grown larva was seen engaged in spinning a slight

silken cocoon about the walls of its prison, which were quite hard and

smooth on the inside, probably owing to the movements of the larva, and

the consequent pressing of the sticky particles to the walls. In a short

time the opening made was closed over by a very thin silken web. The

cells, measured on the inside of the hard walls, were .35 of an inch in

length, and .15 in diameter. The natural attitude of the larva is

somewhat curved in its cell, but if straightened, it just equals the

inside length of the cell. On the 31st of July, two female bees came

out, having cut their way through the sides of their cells." In three

other cells "several hundred minute Ichneumons (Anthophorabia

megachilis) were seen, which came forth as soon as the cells were

opened."

The habits of the little blue or green Mason bees (Osmia) are quite

varied. They construct their cells in the stems of plants, and in rotten

posts and trees, or, like Andrena, they burrow in sunny banks. A

European species selects snail shells for its nest, wherein it builds

its earthen cells, while other species nidificate under stones. Curtis

found two hundred and thirty cocoons of a British species (Osmia

paretina), placed on the under side of a flat stone, of which one-third

were empty. Of the remainder, the most appeared between March and June,

males appearing first; thirty-five more bees were developed the

following spring. Thus there were three successive broods, for three

succeeding years, so that these bees lived three years before arriving

at maturity. This may partly account for _insect years_, which are like

"apple years," seasons when bees and wasps, as well as other insects,

abound in unusual numbers.

[Illustration: 26. Nest of Osmia.]

Mr. G. R. Waterhouse, in the Transactions of the Entomological Society

of London, for 1864, states that the cells of Osmia leucomelana "are

formed of mud, and each cell is built separately. The female bee,

having deposited a small pellet of mud in a sheltered spot between some

tufts of grass, immediately begins to excavate a small cavity in its

upper surface, scraping the mud away from the centre towards the margin

by means of her jaws. A small, shallow mud-cup is thus produced. It is

rough and uneven on the outer surface, but beautifully smooth on the

inner. On witnessing thus much of the work performed, I was struck with

three points: first, the rapidity with which the insect worked;

secondly, the tenacity with which she kept her original position whilst

excavating; and thirdly, her constantly going over work which had

apparently been completed.... The lid is excavated and rendered concave

on its outer or upper surface, and is convex and rough on its inner

surface; and, in fact, is a simple repetition of the first-formed

portion of the cell, a part of a hollow sphere."

The largest species of Osmia known to us is a very dark-blue species (O.

lignivora). We are indebted to a lady for specimens of the bees with

their cells, which had been excavated in the interior of a maple tree

several inches from the bark. The bee had industriously tunnelled out

this elaborate burrow (Fig. 26), and, in this respect, resembled the

habits of the Carpenter bee more closely than any other species of its

genus.

The tunnel was over three inches long, and about three-tenths of an inch

wide. It contracted a little in width between the cell, showing that the

bee worked intelligently, and wasted no more of her energies than was

absolutely necessary. The burrow contained five cells, each half an inch

long, being rather short and broad, with the hinder end rounded, while

the opposite end, next to the one adjoining, is cut off squarely. The

cell is somewhat jug-shaped, owing to a slight constriction just behind

the mouth. The material of which the cell is composed is stout, silken,

parchment-like, and very smooth within. The interstices between the

cells are filled in with rather coarse chippings made by the bee.

The bee cut its way out of the cells in March, and lived for a month

afterwards on a diet of honey and water. It eagerly lapped up the drops

of water supplied by its keeper, to whom it soon grew accustomed, and

seemed to recognize.

Our smallest and most abundant species is the little green Osmia

simillima. It builds its little oval, somewhat urn-shaped cells against

the roof of the large deserted galls of the oak-gall fly (Diplolepis

confluentus), placing them, in this instance eleven in number, in two

irregular rows, from which the mature bees issue through a hole in the

gall (Fig. 27, with two separate cells). The earthen cells, containing

the tough dense cocoons, were arranged irregularly so as to fit the

concave vault of the larger gall, which was about two inches in

diameter. On emerging from the cell the Osmia cuts out with its powerful

jaws an ovate lid, nearly as large as one side of the cell.

[Illustration: 27. Nest of Osmia in a gall.]

In the Harris collection are the cells and specimens of Osmia pacifica,

the peaceful Osmia, which, according to the manuscript notes of Dr.

Harris, is found in the perfect state in earthen cells beneath stones.

The cell is oval cylindrical, a little contracted as usual with those of

all the species of the genus, thus forming an urn-shaped cell. It is

half an inch long, and nearly three-tenths of an inch wide, while the

cocoon, which is rather thin, is three-tenths of an inch long. We are

not acquainted with the habits of the larva and pupa in this country,

but Mr. F. Smith states that the larva of the English species hatches in

eight days after the eggs are laid, feeds ten to twelve days, when it

becomes full-grown, then spins a thin silken covering, and remains in an

inactive state until the following spring, when it completes its

transformations.

In the economy of our wild bees we see the manifestation of a wonderful

instinct, as well as the exhibition of a _limited reason_. We can

scarcely deny to animals a kind of reason which apparently differs _only

in degree_ from that of man. Each species works in a sphere limited by

physical laws, but within that sphere it is a free agent. They have

enough of instinct and reason to direct their lives, and to enable them

to act their part in carrying out the plan of creation.

[Illustration: Paper Wasp.]

FOOTNOTES:

[Footnote 1: The cells are not perfectly hexagonal. See the studies on

the formation of the cells of the bee, by Professor J. Wyman, in the

Proceedings of the American Academy of Arts and Sciences, Boston, 1866;

and the author's Guide to the Study of Insects, p 123.]

[Footnote 2: Notes on the Habits of the Humble Bee (Proceedings of the

Essex Institute, vol. iv, 1864, p. 101).

Mr. Angus also writes us as follows concerning the habits of the

Wandering Humble bee (Bombus vagans): "I have found the males plentiful

near our garden fence, within a hole such as would be made by a mouse.

They seem to be quite numerous. I was attracted to it by the noise they

were making in fanning at the opening. I counted at one time as many as

seven thus employed, and the sound could be heard several yards off.

Several males were at rest, but mostly on the wing, when they would make

a dash among the fanners, and all would scatter and play about. The

workers seem to be of a uniform size, and full as large as the males. I

think the object of the fanning was to introduce air into the nest, as

is done by the Honey bees."]

[Footnote 3: "Since writing the above I have opened one of the new holes

of Xylocopa, which was commenced between three and four weeks ago, in a

pine slat used in the staging of the greenhouse. The dimensions were as

follows:--Opening fully 3-8 wide; depth 7-16; whole length of tunnel 6

5-16 inches. The tunnel branched both ways from the hole. One end, from

opening, was 2 5-8, containing three cells, two with larva and pollen,

the third empty. The other side of the opening, or the rest of the

tunnel, was empty, with the exception of the old bee (only one) at work.

I think this was the work of one bee, and, as near as I can judge, about

twenty-five days' work. Width of tunnel inside at widest 9-16 inch.

"I have just found a Xylocopa bobbing at one of the holes, and in order

to ascertain the depth of the tunnel, and to see whether there were any

others in them, I sounded with a pliable rod, and found others in one

side, at a depth of five and one half inches; the other side was four

inches deep without bees. The morning was cool, so that the object in

bobbing could not have been to introduce fresh currents of air, but must

have had some relation to those inside. Their legs on such occasions

are, as I have noticed, loaded with pollen."]

Our Common Insects A Popular Account of the Insects of Our Fields, Forests, Gardens and Houses · 第 1 / 14 章