CHAPTER I

TRANSCRIBER’S NOTES:

—Obvious print and punctuation errors were corrected.

—Underlined text has been rendered as *underlined text*.

The Cambridge Manuals of Science and Literature

THE FLEA

CAMBRIDGE UNIVERSITY PRESS

London: FETTER LANE, E.C.

C. F. CLAY, MANAGER

[Illustration: LOGO]

Edinburgh: 100, PRINCES STREET

London: H. K. LEWIS, 136, GOWER STREET, W.C.

WILLIAM WESLEY & SON, 28, ESSEX STREET, STRAND

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Leipzig: F. A. BROCKHAUS

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Bombay and Calcutta: MACMILLAN AND CO., LTD.

_All rights reserved_

[Illustration:

_After a drawing by Dr Jordan_

Oriental rat-flea (_Xenopsylla cheopis_ Rothsch.). Male.]

[Illustration; DECORATED FRONT PAGE:

THE FLEA

BY

HAROLD RUSSELL,

B.A., F.Z.S., M.B.O.U.

With nine illustrations

Cambridge:

at the University Press

1913]

Cambridge

PRINTED BY JOHN CLAY, M.A.

AT THE UNIVERSITY PRESS

_With the exception of the coat of arms at the foot, the design on

the title page is a reproduction of one used by the earliest known

Cambridge printer, John Siberch, 1521_

PREFACE

THE aim of this book is to give in plain language some account of a

small, but noteworthy, group of insects. I have avoided, whenever I

could, using the technical terms of zoology. To avoid doing so entirely

is impossible in a book which describes insects in some detail. No

technical term has, I hope, been used without an explanation.

Over thirty years have elapsed since Taschenberg’s German book, _Die

Flöhe_, appeared. Our knowledge has made enormous strides since then.

More species of flea are now known from the British Islands alone

than were then known from the whole world. So far as I am aware, no

book, devoted to what is known about fleas, has ever been published in

English. The statements about these insects in the general text-books

of entomology are frequently antiquated and inaccurate. But there is

a fairly extensive literature on the _Siphonaptera_ scattered through

scientific periodicals mostly in English, German, Italian, Dutch and

Russian. I have given some references in the Bibliography.

The naturalists now living who have devoted any time to the special

study of fleas may almost be counted on one’s fingers. In England there

are Mr Charles Rothschild and Dr Jordan; in the Shetland Islands, the

Rev. James Waterston; in Germany, Taschenberg of Halle and Dampf of

Königsberg; in Russia, Wagner of Kieff; in Holland, Oudemans of Arnhem;

in Italy, Tiraboschi of Rome; in the United States, Carl Baker and a

few others. I have not mentioned medical men who have investigated

fleas in connection with plague.

There are small collections of fleas in the Natural History Museums at

South Kensington (London), Paris, Berlin, Königsberg, Vienna, Budapest,

S. Petersburg and Washington. Of private collections Mr Charles

Rothschild’s at Tring is by far the best in the world. It contains

something like a hundred thousand specimens and is most admirably kept.

I must express profound and sincere gratitude to Mr Rothschild for

having helped me in numberless ways and advised me in many difficulties.

It is well known that the mere mention of fleas is not only considered

a subject for merriment, but in some people produces, by subjective

suggestion, violent irritation of the skin. The scientific study

of fleas has, however, received a great impetus since it has been

ascertained that they are the active agents in spreading plague.

Rat-fleas are of various kinds, and not all fleas will bite man. A

knowledge of the different species has suddenly become useful. The

humble, but ridiculous, systematist with his glass tubes of alcohol for

collecting fleas, his microscopic distinctions, and Latin nomenclature

has become a benefactor of humanity. Some people seem to be practically

immune to the bites of fleas, but even to such persons their visits are

unwelcome. A famous Frenchwoman once declared: “_Quant à moi ce n’est

pas la morsure, c’est la promenade._”

H. R.

LONDON,

_September, 1913_.

CONTENTS

CHAP. PAGE

Preface v

I. Introductory 1

II. The external structure of a flea 21

III. The mouth-parts and sense-organs 38

IV. The internal organs of a flea 52

V. The Human flea and other species 62

VI. The Chigoes and their allies 74

VII. Fleas and Plague 83

VIII. Rat-fleas and Bat-fleas 97

Appendix A. Systematic view of the order _Siphonaptera_ 108

” B. A list of British fleas and their hosts 110

” C. On collecting and preserving fleas 113

” D. Bibliography 118

Index 122

LIST OF ILLUSTRATIONS

Male Oriental rat-flea _frontispiece_

FIGURE PAGE

1. The larva of a flea 6

2. Types of genal and thoracic combs of a flea 26

3. The hind leg of a flea 30

4. The mouth-parts of a flea 43

5. The antenna of a flea 47

6. The alimentary canal of a flea 53

7. The head of a female dog-flea and a female cat-flea 71

8. Pregnant female of _Dermatophilus cæcata_ 81

CHAPTER I

INTRODUCTORY

FLEAS form a group of insects that have, until recently, been little

studied by zoologists. We call them insects because they are jointed

animals, or Arthropods, with three pairs of legs in the adult

condition. The reader will best understand the position which fleas

occupy in the general classification of animals by remembering that

the arthropods, or jointed animals, are one of a dozen subkingdoms, or

phyla, to which the various members of the great animal kingdom have

been assigned. There is good ground for believing that all the animals

included in each phylum trace their ancestry back to a common primitive

form which lived in more or less remote ages. Besides (1) _Insects_,

the arthropods, or jointed animals, include (2) _Crustaceans_, such as

crabs, lobsters, shrimps, wood-lice, water-fleas and barnacles; (3)

_Myriapods_, such as centipedes and millipedes; and (4) _Arachnids_,

such as spiders, scorpions, mites and ticks. To all these varied forms

of animal life fleas, and other insects, are therefore more or less

nearly related.

The animals belonging to this large and important collection, which

compose the arthropod phylum, have certain common characteristic

features. We find a body made up of a series of more or less completely

similar segments placed one behind the other. In this they resemble

certain worms which are far less highly organised. The body is

elongated, symmetrical on either side, and the mouth and anus are at

opposite ends. There is, however, an important advance on the segmented

worms. Each typical segment carries a pair of appendages which are very

different from the foot-stumps that are found on certain worms. These

appendages of arthropods are divisible into distinct limb-segments,

separated from one another by moveable joints, and acted upon by

special muscles.

The common ancestor of all the various arthropods which are found

living on the earth to-day, was probably composed of a series of

segments each very similar to the last and each bearing a pair of very

similar appendages. In the course of ages, these appendages have been

astoundingly modified in form and in function. So it happens that

we find in the arthropods of the present day pairs of antennæ, of

mandibles and other mouth-parts, of pincers, of legs, of swimming-feet

and of tail pieces which on close examination can all be traced back to

a common structure. The body-segments, also, have been strangely fused

together and modified. All that has been so far said applies equally to

fleas and to other insects.

It is of great interest, when one comes to make a minute study of

the form and external structure of a flea, to try and trace the

modifications that must have taken place in the course of descent from

the ancestral arthropod; but the relationship of fleas to other insects

living at the present day is of more immediate concern. Insects are

highly specialized arthropods and fleas are highly specialized insects.

This means that they have become vastly modified from the primitive

ancestral type and fitted thereby for a life among certain defined and

peculiar surroundings.

It will be unnecessary to remind the reader who knows anything of

zoology or of botany that all classification is now based on descent.

Since naturalists have abandoned a belief in the special creation

of the various species of animals now living on the earth and have

conclusively shown that they have arisen by descent and modification

from other forms, the problem is to reconstruct a vast genealogical

tree. What then were the ancestors of the fleas and to what other

insects, in consequence, do they appear to be related?

It is probable that the ancestors of the fleas were winged insects, and

that the organs of flight were gradually lost, as they became useless,

when a partially parasitic life was adopted. At one time entomologists

regarded fleas as wingless flies and placed them in the order Diptera.

Certain supposed scaly plates on their bodies were regarded as the

atrophied relics of wings. It is, however, more than doubtful whether

this view is correct; and all modern entomologists who have given any

special study to fleas are agreed that they are sufficiently unlike

any other living insects to deserve a place in an order by themselves.

To this order the name _Siphonaptera_ has been given: which means that

the insects comprised in it are provided with sucking mouths and are

destitute of wings. Another name for the order is Aphaniptera, but this

is gradually falling into disuse. Linnæus (1758) only mentions two

species of flea: the human flea which he appropriately named _Pulex

irritans_, and the chigoe of hot countries which he called _Pulex

penetrans_, from the habit which the female has of burrowing under the

skin of her victims. At the time of writing, about 460 species of flea

have been described and named; but some of the names are doubtless

synonymous, and the actual number of separable species that have been

discovered is somewhere about four hundred. The vast majority of these

have been described within the last few years, which shows what can be

done when attention is turned to any neglected group of animals. There

can be no doubt that many undiscovered species still remain, and will

now, in due course, be collected, described and named.

The position which should be assigned to the order Siphonaptera in the

general scheme of insect classification is a question on which the most

learned modern entomologists have disputed with considerable vigour.

Some see the nearest relatives among the beetles, others among the

flies. The majority, as we shall see later on, would place them near

the Diptera: but since no convincing arguments have been produced on

either side it may be wisest to regard the question as still at present

unsolved.

Fleas belong to one of the groups of insects which go through a

complete metamorphosis. Their life-history consequently falls into

four divisions: egg, larva, pupa and imago. If the climate permits,

the female flea lays her eggs all the year round, and from one to five

are dropped at a time. Unlike those of many other parasites they are

never attached to the hairs of the hosts, but appear to be deposited

indiscriminately on the floors of houses or in the nests and sleeping

places of their hosts. The eggs generally hatch in a few days, and a

minute, white, wormlike larva emerges (Fig. 1). The larvæ, of some, and

possibly of all, fleas are provided with a wonderful adaptation in the

shape of an egg-breaker or hatching-spine. This is a thin plate, like

the edge of a knife, where the point of the head comes in contact with

the shell. The movements of the prisoner make a slight split in the

egg-shell, which then bursts asunder. This organ has vanished in later

larval life, and it is probably lost after the first moult. The larva

is legless and has thirteen segments. It grows rapidly, and, as it

grows, moults its skin several times. It is provided with mouth-parts

adapted for biting, and eats any decaying organic refuse. The larvæ may

be reared on the sweepings of an ordinary room or the dirty scurf which

collects at the bottom of old birds’ nests. It is hardly necessary to

add that the mother takes no interest whatever in the larvæ and that

the belief that she feeds them on dried blood is not based on any sound

foundations.

[Illustration: Fig. 1. The larva of a flea. The body consists of

thirteen segments and is legless. On the fore part of the head are the

antennæ and on the upper part of the head is shown the knife-like edge

of the egg-breaker. The mouth-parts are adapted for biting. On the last

segment of the body are the two caudal stylets.]

The larval stage lasts some days, and the animal spins a small cocoon

before pupating. In the course of a few more days, the time probably

depending on the weather, the perfect flea emerges. The larvæ generally

live in places where the perfect insects will have an opportunity of

finding a host as soon as they leave the pupal envelope. The nests

of their hosts where the young are being reared are always favourite

places. It seems possible that the comparative immunity from fleas

which hoofed mammals or Ungulates enjoy may be due to the fact that

the young beast follows its mother from the time of birth instead of

passing its early life helpless in a nest.

Observations made on the development of the dog-flea (_Ctenocephalus

canis_) in India show that eggs laid on October 17 hatched on October

19. The larva spun its cocoon on October 25 and the mature flea emerged

on November 2. In Northern Europe the human flea takes about four weeks

in summer and six weeks in winter to pass through its metamorphosis.

Unlike many parasitic insects, fleas do not constantly pass their

time upon the bodies of their victims. The greater part of their

life is probably spent on the ground, in the house, or nest, of the

mammal or bird which serves them with blood. In this respect there is

considerable difference in the habits of different species of flea.

Some attach themselves to an animal and actually burrow into the skin.

These are the most parasitic species. Some only come to feed and leave

to lay their eggs. Many probably do not suck blood more than once in

their lives.

An animal which harbours fleas and which nourishes the adult insect

with blood is called a _host_. No fleas are more than what is called

temporary parasites; which means that they pass but a portion of their

lives on their hosts and frequently take occasion to hop on and off.

All fleas, apparently, go from host to host. The labours of diligent

collectors have proved that the great majority of mammals and birds

have fleas. As a general rule, it is true to say that certain species

of flea are associated with certain species of host. Thus man is the

true host of _Pulex irritans_; the cat family are the true hosts of

the cat-flea (_Ctenocephalus felis_); and the dog family are the true

hosts of the dog-flea (_Ctenocephalus canis_). But the human flea is

sometimes found on cats and dogs, and cat and dog-fleas occasionally

bite human beings; and cat-fleas are found on dogs and dog-fleas are

found on cats. All fleas, so far as we know, may occasionally pass from

one species of host to another; but they do not, for the most part,

seem to flourish in unaccustomed quarters. Some fleas are more catholic

in their tastes than others. Some seem to be very strictly confined to

one host, and even when starving only suck strange blood under protest.

There is a species of flea that has only (except by accident) been

found on the long-tailed field-mouse and another that has only been

found on the hedgehog. Other fleas are commonly found on two absolutely

distinct animals; a good instance of this is the human flea which, at

all events in certain parts of England, is a regular parasite of the

badger.

As distinguished from true or natural hosts one must separate what

may be termed casual or accidental hosts. All animals which come in

contact with one another, or which live in close proximity, may

exchange fleas. So even bird-fleas may be collected from mammals and

typically mammalian fleas from birds. In this fashion puzzles may

arise which tax the ingenuity of the collector to solve. Bird-fleas

are sometimes found on bats, and this may be obviously attributed to

the bats having inhabited a hole which was tenanted by starlings or an

old loft infested with the fleas of pigeons. All beasts of prey are

sometimes found to harbour the fleas of animals they have devoured.

Rabbits’ fleas are found on wild-cats; hedgehogs’ fleas on foxes; mice

fleas on weasels; and fleas characteristic of small birds on stoats.

So also in the case of mice, rats and voles with holes and runs in the

same hedgerow, the parasites usually peculiar to one are not uncommonly

found on the others. It is sometimes difficult to determine the true

host of a flea.

Much more puzzling to explain are the reasons which confine a flea to

a certain host and which cause closely allied hosts to have different

fleas. The fleas from the house-martin and the sand-martin are quite

different; those from the domestic fowl and the domestic pigeon are

distinct species. The causes which have affected the evolution of the

various forms of flea are too obscure to enable anyone at the present

day to offer any satisfactory explanation.

Speaking generally, the fleas found on birds have points in common,

and they probably form a natural group to themselves. What may be

called true bird-fleas have been collected from almost all European

birds. An unwieldy genus (_Ceratophyllus_) comprises many species of

different flea. Some species are very abundant and infest the nests of

many different birds. Others are extremely rare. One of these rarities

(_C. vagabundus_) is found in the nests of puffins and other sea-birds.

Another has been collected on antarctic petrels. Penguins have a

special genus of flea to themselves. A specimen, unique at one time

(_Ceratophyllus borealis_), in Mr N. C. Rothschild’s collection was

obtained from the gannet. It has now been found on rock-pipits in the

Shetland Islands.

Two very rare fleas (_C. farreni_ and C. _rothschildi_) are found in

the nests of house-martins; yet the nests of these birds are infested

with common species besides. A plague flea (_Xenopsylla_) has been

found on an African swift.

Forty-six different species of flea have been found in the British

Islands, but many of these are extremely scarce.

We know too little about the geographical distribution of fleas to lay

down many accurate generalities. When a great deal more material has

been collected and studied, it may be possible to show that certain

groups are associated with certain regions of the earth or certain

orders of animals. To some extent this is already seen to be the case.

The fleas indigenous to the New World are distantly related to those

of the Old World. Broadly speaking the geographical distribution of the

parasite must follow that of the host. But sometimes the parasite is

impatient of cold and cannot follow the host out of the tropics. The

chigoes and their allies are fleas of hot countries. Different kinds

of bats are found from the tropics to the Arctic circle, but the same

bat-fleas are not found everywhere.

When a flea has a cosmopolitan range it is probable that it has

travelled over the world in company with its host.

Monkeys have no fleas. This is an assertion that is commonly received

with surprise and incredulity. Occasionally a gorilla or a chimpanzee

may get a chigoe in its toe. And monkeys in zoological gardens or

menageries are possibly exposed to the danger of catching an occasional

human flea from the people who crowd round their cages. These are

remote contingencies which may happen to anyone. Healthy wild monkeys

are much too clean and active to harbour fleas. When they search one

another’s fur in a fashion that must be familiar to most persons, they

are clearing their coats of particles of scurf or of similar scraps of

dirt and not of fleas. So, speaking generally, it may be said that no

fleas have been found truly parasitic on monkeys.

Bats have fleas, but not in great abundance. All bat-fleas are rare

on their hosts and extremely difficult to find and collect. The

same species are not found on fruit-bats and the ordinary smaller

insect-eating bats. The geographical distribution of some bat-fleas is

puzzling. For instance, one species (_Ischnopsylla unipectinata_) is

found on the greater horse-shoe bat in Europe; but it is, apparently,

not found on the same bat in the British Islands. In Somaliland and in

India it is found on other bats.

With certain exceptions, Ungulates are remarkably free from fleas. This

great order of mammals includes a variety of hoofed animals: oxen,

sheep, goats, deer, pigs, camels, giraffes and antelopes.

The only true fleas found on these are two species of the genus

_Vermipsylla_, which resemble the chigoes in so far that the pregnant

females burrow into the host and expand there. One species has been

found on camels and horses in Transcaucasia; another on roe-deer in

Northern China. The female of the last is often found ensconced on

the inside of the nostrils of the deer. Of course chigoes may attack

domestic Ungulates of all kinds; but no other members of the family

_Pulicidæ_ or typical fleas except those two above mentioned have been

found on hoofed mammals.

Insectivora such as moles, shrews and hedgehogs are the hosts of a

great variety of species. The same thing may be said of the Rodents,

which include porcupines, squirrels, rats, mice and a vast number of

other small mammals whose geographical distribution includes almost the

whole of the habitable globe. Probably more different species of fleas

have been collected from Insectivora and Rodents than from all the

other orders of mammals grouped together.

The Carnivora, excluding the Pinnepedia, or seals, sea-lions and

walruses, harbour numerous species.

Among the Edentata a very remarkable and highly specialised genus

of fleas is parasitic on armadilloes in South America. This genus

(_Malacopsylla_) consists of two species only, which are confined to

South America and are found on the armadilloes and on carnivorous

animals which probably have preyed on them. The thorax of these fleas

is much reduced and very small in size. Their piercing organs are

slender and weak, but they possess enormous spines on the legs with

which they hold on to their hosts. These two South American fleas (_M.

grossiventris_ and _M. androcli_) will be referred to again later as

striking examples of fleas with strongly developed legs and weakly

constructed mouth-parts. The contrary combination of powerful mouths

and degenerate legs is also found in other groups of fleas, as will be

seen in the chapter on the chigoes.

The Marsupials of Australia and South America have special fleas which

were probably associated with this strange order of pouched mammals

before they became divided into the American and Australian groups.

Fleas have been collected on the spiny ant-eater (_Echidna_) which

belongs to the lowest order of Monotremes or egg-laying mammals.

On almost every form of bird, including the most aquatic kinds, fleas

of various species have been obtained.

Only one instance has been recorded of a flea occurring on a reptile.

A female of one of the species of burrowing chigoes (_Echidnophaga

ambulans_) from Australia was collected by Dr Woodward from the Brown

Snake (_Diemenia superciliosa_). This reptile, which is well known

in Australia, belongs to a sub-family that contains some of the most

deadly poisonous snakes and is allied to the cobras. The Brown Snake is

a terrestrial snake, and one must regard the presence of the flea on

such a host as a rare and chance occurrence. The snake was captured at

Herdman’s Lake, near Perth in West Australia. The same species of flea

has also been obtained from the phalangers (_Trichosurus_) which live

in the tops of the Australian gum-trees; from the little terrestrial

and nocturnal rat kangaroos (_Bettongia_); and from the banded

ant-eater (_Myrmecobius_), another Australian Marsupial. It is possible

that the flea moved from some small mammal which was being devoured by

the snake and managed to fix itself between the scaly plates of the

reptile.

When fleas are hatched in a nest they have no choice but to attach

themselves to the young mammals or birds. But even in that case

they frequently leave their hosts and do not for very long remain

stationary. Moreover, when a host dies and becomes cold the fleas

invariably leave their quarters, which explains how it may happen that

Carnivora get infested with the fleas of their prey. This change of

hosts which is always occurring makes it impossible to draw conclusions

from material collected in zoological gardens where many animals are

herded together. In menageries, too, the normal conditions of breeding

are absent. A German naturalist collected 2036 fleas from theatres,

concert-halls, ball-rooms, schools and barracks in the grand-duchy

of Baden and found that more than fifty per cent. were dog-fleas

(_Ctenocephalus canis_). What the proportion may be in other parts

of Europe we have no materials from which to form a judgment. In

zoological gardens cat-fleas (_Ct. felis_) are generally numerous in

most of the cages.

It is, of course, well known to every zoologist that species are not

fixed or constant and that various forms of mammal or of bird tend to

show geographical variations. When a long series of skins are laid out

on a table and carefully examined it is seldom that those from the west

of any great region cannot be picked out and distinguished from those

obtained in the east. So we also get northern and southern forms of

the same species varying slightly. These variations are perceptible in

many forms of insects, and zoologists now describe these local races as

subspecies and designate them with trinomials. No one, however, knows

enough as yet about all the various forms which are assumed by fleas

to attempt, except in a few instances, to do so in the case of these

animals.

The study of Siphonaptera is still quite in its infancy. We know little

or nothing of the minute geographical variation of fleas. That there

is such a thing can already be seen in a few species. In the meantime

the study of variation must be postponed until collectors have amassed

a more plentiful amount of material; and it is best to treat all forms

which are to all appearance constantly different as being specifically

distinct until more is known about variation.

Any classification of fleas that may now be attempted can only be

tentative. It will be enough for present purposes if the reader will

remember that the Order Siphonaptera can be divided into three groups

or families: (1) the chigoes and their allies, which are the most

parasitic fleas (_Sarcopsyllidæ_); (2) the typical fleas to which

the majority of species belong (_Pulicidæ_); and (3) the bat-fleas

(_Ceratopsyllidæ_), which have certain peculiarities that will be

described in a later chapter.

Of the antiquity of fleas, and of the period in geological history when

the order made its appearance, little can be said. When it was thought

that fleas were confined, as parasites, to warm-blooded mammals and

birds, evolutionists were inclined to say that the parasites could

not have appeared before their hosts. The discovery of a flea on a

reptile opened the vista of possibly enormous antiquity stretching back

to Permian or Carboniferous ages. The fossil record is most meagre.

If we reject as too doubtful the supposed remains of a flea from the

lower Oligocene strata at Aix in Provence, only one undoubted fossil

has been discovered. Nor does it seem certain that fleas are entirely

restricted to preying on vertebrates. Dr Dampf introduced a number

of common bird-fleas (_Ceratophyllus gallinæ_) of both sexes to some

hairy caterpillars. He observed that several of the fleas buried their

heads in the hairy covering of the larvæ and remained some time in the

attitude of sucking blood. While this was going on the victims made

violent demonstrations of annoyance and discomfort. He also observed

that a naked caterpillar was not attacked.

Mr Boden has also recorded how he found in a seed-warehouse some

peas that were being eaten by two species of Lepidopterous larvæ. On

bringing these home and keeping them in a jar, he found among them

some small larvæ which ultimately turned into fleas, probably _Pulex

irritans_. These fleas, being confined without other food, were

observed to prey on the Lepidopterous larvæ and to feed freely on

their juices. The larvæ which were attacked by fleas pined and died.

The fluid from the stomach of the fleas when they were crushed was

transparent and not red like vertebrate blood which often exudes when a

mammalian flea is pinched and cracked open.

A French entomologist has also reported that the numerous fleas which

swarm in the dwelling-houses of Corsica, for want of other nourishment

turn their attention to flies that may be incapable of flight.

The only fossil remains of a flea that have, so far, been discovered

are a single insect in a piece of Baltic amber of Oligocene age. Many

organic remains have been preserved in this fashion, but this is the

first mammalian parasite that has been found. The flea is admirably

protected by its semi-transparent surroundings, and the most minute

details of structure, the arrangement of bristles on the body, and the

number of segments to the labial palpi can be discerned. This unique

object is in the collection of Professor Klebs. The first point to

note is that a flea of this antiquity hardly differs from the existing

insects of the present day. It has been referred to an existing genus

(_Palæopsylla_) of which there are at least four species living.

Three of these are parasites of the mole, and the fourth is found on

shrews. There is good reason to suppose that the host of the fossil

was some insectivorous mammal. The early specialisation of fleas is

strikingly illustrated. This insect is already adapted for life on

some warm-blooded animal. It has a thoracic comb, and its mouth-parts

are in all respects like those of a modern flea. It belongs to a genus

which is still commonly distributed over Europe. When we consider how

remote are the chances that a mammalian flea should first get embedded

in amber and should, subsequently, be detected and described by a

naturalist, we may well understand that the owner of the fossil asked,

though without success, £1200 for it.

The ordinary person regards fleas as a subject for humour of an obvious

and familiar kind. The utilitarian despises a man who can cheerfully

spend his time in collecting fleas. Yet it seems probable that a study

of their forms and habits may be of immediate benefit to the human

race. The discovery that fleas are connected with the spread of plague

is an instance of apparently unprofitable scientific labour proving of

direct advantage to mankind. An accurate knowledge of the structure

and habits of fleas is now seen to be of importance to all who are

engaged in fighting one of the most dreaded infectious diseases. When

plague breaks out men of science now at once turn their attention to

the fleas. This is likely to prove more directly efficacious than the

mediæval custom of marking the house with a red cross and inscribing

the legend, “God have mercy on us.”

The Flea · 第 1 / 8 章