CHAPTER I

HOW TO KNOW

THE FERNS

BY

S. LEONARD BASTIN

WITH THIRTY-THREE ILLUSTRATIONS

METHUEN & CO. LTD.

36 ESSEX STREET W.C.

LONDON

_First Published in 1917_

CONTENTS

CHAP. PAGE

I. The Ferns and their Allies 1

II. Life Histories 13

III. Yesterday and To-day 23

IV. Three Dainty Ferns 33

V. The Bracken Fern and Two Interesting Species 38

VI. The Male Fern and its Relatives 46

VII. The Lady Fern and the Spleenworts 66

VIII. The Polypodies 86

IX. The Royal Fern 93

X. Four Curious Ferns 96

XI. The Club Mosses 101

XII. The Horsetails 112

XIII. Fern Collecting and Preserving 122

XIV. The Culture of Ferns 129

Index 133

LIST OF ILLUSTRATIONS

PAGE

The Bristle Fern 34

The Tunbridge Filmy Fern 36

The Bracken Fern 39

The Maidenhair Fern 42

The Maidenhair Fern (Enlarged view of Back of Frond) 43

The Male Fern 47

The Mountain Buckler Fern 51

The Mountain Buckler Fern (Enlarged) 52

_Nephrodium dilatatum_ 54

The Holly Fern 58

The Oblong Woodsia 62

The Brittle Bladder Fern 64

_Athyrium filix-fæmina_ 67

The Rue-leaved Spleenwort 71

The Rue-leaved Spleenwort (Enlarged Back of Frond) 72

The Sea Spleenwort 76

The Maidenhair Spleenwort 79

The Green Spleenwort 81

The Hartstongue 82

The Sori on the Back of a Hartstongue Frond 83

The Common Polypody 87

Enlargement of the Sori on the Frond of Common Polypody 88

The Beech Fern 89

The Royal Fern 94

The Adder’s Tongue 97

The Moonwort 99

The Common Club Moss 102

The Fir Club Moss 104

The Quillwort 108

_Azolla caroliniana_ 110

Barren Stem of _Equisetum arvense_ 113

Fertile Cones of _Equisetum maximum_ 115

The Dutch Rush 120

HOW TO KNOW THE

FERNS

CHAPTER I

THE FERNS AND THEIR ALLIES

In its lowest forms vegetable life is a very simple affair. The minute

Algæ which clothe damp surfaces with a green film show few indeed of the

characteristics with which we are familiar in the higher plants.

Certainly they are green, proving that the tiny cells of which they are

composed contain the wonderful colouring matter—chlorophyll, by means of

which they are able to assimilate carbon from the carbonic acid of the

air. There is, however, in these lowly plants no sign of a stem, a leaf,

or a root. As we ascend in the scale of vegetable life we begin to get an

increasing number of distinctive characters. In the case of the Mosses we

have plants with distinct stems and leaves. But Mosses have no true

roots, neither is there any vascular (woody) tissue in their composition.

Mounting yet higher in the scale we come to a very important and

interesting group of plants usually referred to as the Vascular

Cryptogams. In this group are included the Ferns, the Horsetails, and the

Club Mosses. In passing, it may be pointed out that the term Cryptogam is

a name which was originally given to the flowerless plants by Linnæus to

indicate that the plan of fertilization was hidden. The name is still

retained, but it has lost its meaning in this sense, in that since the

introduction of high-power microscopes it is not necessarily more

difficult to study the fertilization of the non-flowering plants than it

is to watch the process in the kinds which bear blossoms.

A small acquaintance with the Vascular Cryptogams will show us that they

approach very closely to the flowering plants, or Phanerogams, as they

are called, in their general features. It is true that in the cases of

the Club Mosses and Horsetails the leaves are small or very poorly

developed, but with the Ferns the foliage is often of an advanced type.

All the Vascular Cryptogams, apart from a few insignificant exceptions,

produce real roots; and, as the name implies, in a botanical sense,

evidence woody tissue in their composition. Whilst the Club Mosses and

Horsetails are comparatively humble plants, the Ferns have reached a

remarkable development in the arboreal species. These, of course, grow

into large trees which may be fifty or more feet in height, with thick

woody trunks. Our common Male Fern not infrequently forms a short

trunk-like stem if it is allowed to remain in an undisturbed state for a

number of years. Not all the Ferns are large or even of moderate size;

many of the Filmy Ferns are so minute that they are often taken for

Mosses by those who do not know any better.

All the Vascular Cryptogams show an alternation of generation; that is,

in the life history of each plant there is a sexual and an asexual

individual. As is fully explained later, the plant which arises from the

spore of the Vascular Cryptogam is quite an insignificant body known as

the prothallus. This has a comparatively short existence in most cases.

It is on the prothallus, however, that the sexual organs are produced,

and after fertilization the plant as we know it arises. This individual

is called the sporophyte. The plant is responsible for the spores which

are produced in little cases called sporangia. These are borne straight

on the leaves, and are produced without anything in the way of

fertilization having taken place. As far as the Ferns are concerned, the

spores are all of one kind, but in certain of the Club Mosses two kinds

of spores are produced.

Apart from a few exceptions the Vascular Cryptogams are mostly perennial

in habit. In many cases other means of reproduction are available than

the agency of spores. It is believed that the Bracken Fern is rarely

reproduced by its spores. The increase of this plant seems to be very

effectively carried out by means of the strong growing underground stems

which shoot about in all directions. The Horsetails commonly propagate

themselves in the same way, and it is this which makes them so difficult

to eradicate in the garden. In the case of many Ferns a common mode of

increase is that of budding off new plants on the leaf. The well-known

New Zealand species, _Asplenium bulbiferum_, produces little buds on its

fronds; these grow into small plants, so that each leaf may be

responsible for dozens of new individuals. An even more singular case is

the so-called Walking Fern from North America (_Scolopendrium

rhizophyllum_), which bears long, tapering leaves something like our

Hartstongue. These bend over in such a way that their tips touch the

ground; on the point of the frond a bud is developed. Roots go down into

the soil from the point of the frond, leaves shoot upwards, and thus a

new plant is born. In some species of Club Moss the increase of the plant

by spore production is supplemented by a plan which involves the bearing

of bulbils on the shoots. These are vegetative processes which give rise

to new individuals when they tumble to the ground.

It is of interest to consider the general characteristics of the members

of the Fern tribe. As a rule the stem is either in the nature of a short

underground process bearing a rosette of leaves, as in the case of the

Male Fern and Hartstongue, or there is a horizontal stem more or less

below the surface of the soil, such as is to be seen in the case of the

Bracken Fern and the Polypody. Sometimes the stem assumes the proportions

of a trunk, but these Tree Ferns only occur in the tropics. Where the

stem of the Fern is upright it is properly termed a caudex, whilst in its

horizontal form it is spoken of as a rhizome. There is actually some

doubt as to the real nature of the frond of the Fern. Some botanists are

inclined to believe that it is not really a leaf at all, but is a

modified stem structure. Those who hold this view consider that the

curious scaly structures so common amongst Ferns are really the leaves of

the plant. Here the matter must be left on the present occasion, as it is

proposed to use the terms leaf and frond as meaning the same thing.

An outstanding feature in the case of most Ferns is the remarkable manner

in which the fronds are subdivided. In the case of the Male Fern it is

seen that the upper part of the stalk, or rachis, as it is called, bears

two rows of leaflets. These leaflets are properly referred to as pinnæ.

When the leaflets are subdivided the divisions are spoken of as pinnules.

These pinnules may be deeply lobed, and when this is the case each lobe

is called a segment. In very large fronds the pinnules are again divided;

the frond is then said to be tri-pinnate. Sometimes towards the top of

the pinnæ or the frond the divisions become less pronounced; this

character is designated pinnatifid. It should be noticed that the lower

portion of the stalk, on which there are no pinnæ, is called a stipes. Of

course in some cases, as with the Hartstongue, the leaf is quite

undivided, without even any very pronounced indentations on the margin.

The unrolling of the Fern frond is a very beautiful process. Where the

leaf is not divided in any way the process of expanding resembles the

uncoiling of a watch-spring. Even where there are divisions the unrolling

goes forward in the same manner with each subdivision, even down to the

lobes. This particular mode of unfolding is called circinate. The texture

of the leaves of Ferns is mostly thin and delicate, so that apart from

some exceptions the foliage is not able to withstand the action of dry

air. A notable feature with a large number of Ferns is the length of time

which the leaves take to develop. The fronds of the Male Fern, for

instance, start in the bud at least two years before they actually

unfold. An examination will show that the roots of the Male Fern spring

from the frond bases. It will be found that the position of the roots is

the same in all Ferns.

With all Ferns the production of spores is confined to the leaves. In

many instances there is no distinction between the fertile and the barren

leaves. The stem does not start at once to produce leaves bearing the

sporangia or spore cases. Thus, in the very young Fern the fronds are

always barren; as the stem becomes older, fertile fronds are produced. In

some cases the sporangia are borne on distinct leaves, as in the case of

the Hard Fern, or on special parts of the leaves, in the manner to be

seen in the Royal Fern. The difference in such cases is not really a very

important distinction. A careful examination of the fertile portion of a

Royal Fern frond will show a small amount of green tissue, or mesophyll,

as it is called, at the lower portion of the pinnæ. Actually the fertile

leaf, or part of a leaf, is similar to the barren portions, save that it

produces a much reduced amount of green tissue or, in some cases, perhaps

none at all.

In general appearance the Club Mosses bear a resemblance to the true

Mosses, and hence the popular name, which is certainly rather misleading.

With these plants the leaves are small and almost bristle-like, and are

gathered closely round the stem. In many of the Club Mosses a large part

of the stem lies closely along the ground, and from this at intervals

roots are sent down into the soil and leafy shoots rise upwards. The

sporangia are produced on special leaves, which are usually gathered

together in the form of cones.

Although they vary somewhat in size, all the Horsetails are striking

plants. Here there is a branching underground rhizome from which arise

the aerial stems. The most distinctive feature of the plant are the

whorls of smaller branches which arise from the joints of the main stem.

These carry on the work which is usually assigned to the foliage of the

average plant,—that is, the assimilating of carbon from the carbonic acid

of the atmosphere. The real leaves of the Horsetail are much reduced in

size, and take very little part in the work of nutrition. We shall find

them at the joints of the stem as rings, each collection forming a kind

of sheath. The leaves, which are usually of the same number as the

branches, show no sign of their individuality, save in the little

projecting teeth. In some species the fertile shoots, which appear in the

form of cones, are produced specially. These appear in the spring before

the ordinary vegetative growths, and are quite destitute of chlorophyll.

In other species the normal green shoots are fertile at the termination.

The sporangia are borne on curious scale-like leaves, a large number of

which go to the making of a cone.

One or two aquatic plants, which belong to the Vascular Cryptogams, call

for comment. The Pillwort is a singular plant not uncommon in damp

situations. The leaves of this plant are narrow, and the spores are

produced in curious rounded processes. The Water Fern (_Azolla_) is an

introduced plant which sometimes grows abundantly on lakes in the South

of England. Both the before-mentioned plants are allied to the Ferns. The

Water Club Mosses (_Isoëtes_) are represented in this country by a

species commonly known as the Quillwort. This plant grows in lakes, and

is easily recognized by its quill-like foliage.

Owing to the large number of species a somewhat elaborate classification

is necessary in the case of Ferns. In distinguishing the different

families, the manner in which the collections of spore cases, known as

sori, occur, as well as the features which the individual sporangia

present, are important guides. The actual position of the sorus on the

leaf, the presence or absence of a covering (indusium), are also

distinctive features, both in the families and sub-families. When the

individual sporangium is examined it is found that there is often present

an annulus, a special ring of cells which plays an important part in the

rupturing of the case. The extent of this ring or (as sometimes happens)

its absence will alike be a decisive factor in fixing the family to which

a species belongs. In some families a prominent feature is the fact that

the sporangium has little or no stalk, although this is the exception

rather than the rule. For a more complete description of the sporangium

of the Fern the reader is referred to a succeeding chapter. It is

certainly helpful to a study of these beautiful plants to try to fix in

the mind the families, and their characters, of the order _Filices_. In

all there are eight families belonging to the Fern tribe. These are given

in the order in which they occur in technical books.

1. _Hymenophyllaceæ._—The Filmy and Bristle Ferns. This family includes

some of the simplest kinds of Ferns. There are only three representatives

in the United Kingdom. These are _Hymenophyllum tunbridgense_, _H.

Wilsoni_, and _Trichomanes radicans_. The two former species are fairly

common on rocks which are splashed with water, but the latter seems only

to occur in restricted districts in the South of Ireland. All the species

must have an abundance of water, or the foliage quickly shrivels. This is

due to the fact that the leaves consist of a single layer of cells and

are, of course, very thin. A distinctive feature in this family is the

bearing of the sporangia; these are almost or entirely stalkless. The

sorus, as the group of sporangia is called, is surrounded by an enclosure

from the leaf margin. In _Trichomanes_ this is cup-shaped, whilst in

_Hymenophyllum_ it is bivalved. The popular name Filmy Fern—bestowed on

the Hymenophyllums and allied species—has reference to the

semi-transparent nature of the fronds. In the case of _Trichomanes_ the

axis on which the sporangia are inserted often projects beyond the cup in

which they are contained. This gives a curious spiky appearance to the

fertile frond, and hence the name Bristle Fern.

2. _Polypodiaceæ._—This is a very large family, containing two or three

times as many species as all the rest of the Vascular Cryptogams put

together. Nearly all our native species, with a few exceptions, belong to

the family. A distinctive feature is the incomplete annulus of the

sporangium. Another point to notice is that the spore cases are stalked.

So large is the family that it has been divided into a number of

sub-families; the members of these are chiefly characterized by the

position of the sorus, the cluster of sporangia on the back of the frond.

The different sub-families may be briefly outlined.

(_a_) _Davalliaceæ._—There are no British representatives of this family.

In this case the sorus is always near to the margin of the leaf, and the

indusium or covering is cup-shaped. A familiar species is _Davallia

bullata_ from the East; the rhizomes of this Fern are trained into

various shapes by the Japanese.

(_b_) _Pterideæ._—The Bracken Fern (_Pteris aquilina_), the Maiden Hair

(_Adiantum capillus-veneris_), and the Parsley Fern (_Cryptogramme

crispus_) belong to this sub-family. A notable feature of the Bracken is

the continuous marginal sorus. There is no proper indusium, but the leaf

margin curls over and protects the sporangia to some extent.

(_c_) _Aspidieæ._—The sorus is in the form of a little rounded heap. The

indusium, which is usually kidney-shaped, is supported by a central

stalk, somewhat after the manner of a nasturtium leaf. The Male Fern

(_Nephrodium filix-mas_) belongs to this sub-family, as well as the

Bladder Ferns (_Cystopteris_) and the _Woodsias_.

(_d_) _Asplenieæ._—Here the sorus is elongated or linear. The indusium

arises from a vein to which the sorus is attached. Some very charming

Ferns belong to this sub-family. Many botanists include the Lady Fern

(_Athyrium filix-fæmina_) in this section. Certain of the Spleenworts

(_Asplenium_) are common. The Wall Rue (_A. ruta-muraria_) and the Black

Maidenhair Spleenwort (_A. adiantum-nigrum_) are well known.

(_e_) _Polypodieæ._—The sori on the underside of the leaves are without

any indusium. They are in rounded clusters, and look like small buttons.

_Polypodium vulgare_ is one of our commonest Ferns. Some of the other

species of this genus, such as the Oak Fern (_P. dryopteris_) and the

Beech Fern (_P. phegopteris_), are abundant in some localities.

(_f_) _Grammitideæ._—The Gold and Silver Ferns. The only British species

is the Annual Maidenhair (_Gymnogramma leptophylla_). The plant occurs in

the Channel Islands. This species is one of the few Ferns which are not

perennial. The sori, which follow the veins, have no indusium.

(_g_) _Acrosticheæ._—There are no British representatives of this

sub-family. In this case the whole of the underside of the leaf is

covered with sporangia, and there is no indusium.

3. _Cyatheaceæ._—There are no British representatives of this family,

which is interesting, owing to the fact that it includes the Tree Ferns.

4. _Gleicheniaceæ._—A group of Ferns which are almost entirely tropical.

5. _Schizæaceæ._—Another tropical family.

6. _Marattiaceæ._—A family of large and handsome Ferns, the members of

which occur in the tropics. There are not many representatives of this

family nowadays, but remains in the Coal Measures show that the species

were very much more numerous in Palæozoic times.

7. _Osmundaceæ._—A small family, but rather an important one, owing to

the fact that a leading representative, the Royal Fern (_Osmunda

regalis_), is so well known. In this species only the upper portion of

the leaf is fertile. The sporangia have very short stalks, and are not

provided with an annulus at all. They burst open in a longitudinal slit,

opposite to a special group of cells just below the apex. The sorus has

no indusium.

8. _Ophioglosseæ._—This family is represented by three British species,

of which the Moonwort (_Botrychium lunaria_) and the Adder’s Tongue

(_Ophioglossum vulgatum_) are best known. There is much doubt as to

whether this family can be properly included amongst the Ferns at all. We

may here give them the benefit of the doubt. The leaves in these species

are unfolded from the sides—a totally distinct plan from that to be

observed in all the Ferns which have been described, where the frond and

its divisions are unrolled upwards. The prothallus is a small underground

body destitute of chlorophyll. The fertile leaves are distinguished from

the barren ones by the production of a special branch which bears the

fructification. The sporangia are large.

The next order of the Vascular Cryptogams is of comparatively small

importance as far as the present study is concerned. It is known as the

_Rhizocarpeæ_ (Pepperworts). The order is divided into two families as

follows:—

1. _Salviniaceæ._—The only two genera are Salvinia and Azolla; the latter

has been already mentioned.

2. _Marsiliaceæ._—The British example is the Pillwort (_Pilularia

globulifera_).

The Club Mosses have been divided into six families. Two of these—the

_Lepidodendraceæ_ and the _Sigillariaceæ_—are only represented by

fossils; and one, _Psilotaceæ_, has no British representatives. The

remaining families all include one or more species which are indigenous

to our islands.

1. _Lycopodiaceæ._—These are the Club Mosses proper. Several species of

the genus _Lycopodium_ are British. The Common Club Moss (_Lycopodium

clavatum_) is often abundant on high moors.

2. _Selaginellaceæ._—A large family containing three or four hundred

species, only one of which, however, is British; this is _Selaginella

spinosa_.

3. _Isoëtaceæ._—A family of aquatic Club Mosses. The British species is

_Isoëtes lacustris_, a plant which is sometimes common in the northern

lakes.

With this brief survey of the Vascular Cryptogams one may naturally pass

to a somewhat more detailed consideration of the life histories of these

interesting plants than it has been possible to give in an opening

chapter.

How to Know the Ferns · 第 1 / 14 章