This afternoon, strolling through the under-cliff, I have come across

two quaint and rather uncommon flowers among the straggling brushwood.

One of them is growing like a creeper around the branches of this

overblown gorse-bush. It is the lesser dodder, a pretty clustering mass

of tiny pale pink convolvulus blossoms. The stem consists of a long red

thread, twining round and round the gorse, and bursting out here and

there into thick bundles of beautiful bell-shaped flowers. But where

are the leaves? You may trace the red threads through their

labyrinthine windings up and down the supporting gorse-branches all in

vain: there is not a leaf to be seen. As a matter of fact, the dodder

has none. It is one of the most thorough-going parasites in all nature.

Ordinary green-leaved plants live by making starches for themselves out

of the carbonic acid in the air, under the influence of sunlight; but

the dodder simply fastens itself on to another plant, sends down

rootlets or suckers into its veins, and drinks up sap stored with

ready-made starches or other foodstuffs, originally destined by its

host for the supply of its own growing leaves, branches, and blossoms.

It lives upon the gorse just as parasitically as the little green

aphides live upon our rose-bushes. The material which it uses up in

pushing forth its long thread-like stem and clustered bells is so much

dead loss to the unfortunate plant on which it has fixed itself.

Old-fashioned books tell us that the mistletoe is a perfect parasite,

while the dodder is an imperfect one; and I believe almost all

botanists will still repeat the foolish saying to the present day. But

it really shows considerable haziness as to what a true parasite is.

The mistletoe is a plant which has taken, it is true, to growing upon

other trees. Its very viscid berries are useful for attaching the seeds

to the trunk of the oak or the apple; and there it roots itself into

the body of its host. But it soon produces real green leaves of its

own, which contain the ordinary chlorophyll found in other leaves, and

help it to manufacture starch, under the influence of sunlight, on its

own account. It is not, therefore, a complete drag upon the tree which

it infests; for though it takes sap and mineral food from the host, it

supplies itself with carbon, which is after all the important thing for

plant-life. Dodder, however, is a parasite pure and simple. Its seeds

fall originally upon the ground, and there root themselves at first

like those of any other plant. But, as it grows, its long twining stem

begins to curl for support round some other and stouter stalk. If it

stopped there, and then produced leaves of its own, like the

honeysuckle and the clematis, there would be no great harm done: and

the dodder would be but another climbing plant the more in our flora.

However, it soon insidiously repays the support given it by sending

down little bud-like suckers, through which it draws up nourishment

from the gorse or clover on which it lives. Thus it has no need to

develop leaves of its own; and it accordingly employs all its stolen

material in sending forth matted thread-like stems and bunch after

bunch of bright flowers. As these increase and multiply, they at last

succeed in drawing away all the nutriment from the supporting plant,

which finally dies under the constant drain, just as a horse might die

under the attacks of a host of leeches. But this matters little to the

dodder, which has had time to be visited and fertilised by insects, and

to set and ripen its numerous seeds. One species, the greater dodder,

is thus parasitic upon hops and nettles; a second kind twines round

flax; and the third, which I have here under my eyes, mainly confines

its dangerous attentions to gorse, clover, and thyme. All of them are,

of course, deadly enemies to the plants they infest.

How the dodder acquired this curious mode of life it is not difficult

to see. By descent it is a bind-weed, or wild convolvulus, and its

blossoms are in the main miniature convolvulus blossoms still. Now, all

bind-weeds, as everybody knows, are climbing plants, which twine

themselves round stouter stems for mere physical support This is in

itself a half-parasitic habit, because it enables the plant to dispense

with the trouble of making a thick and solid stem for its own use. But

just suppose that any bind-weed, instead of merely twining, were to put

forth here and there little tendrils, something like those of the ivy,

which managed somehow to grow into the bark of the host, and so

naturally graft themselves to its tissues. In that case the plant would

derive nutriment from the stouter stem with no expense to itself, and

it might naturally be expected to grow strong and healthy, and hand

down its peculiarities to its descendants. As the leaves would thus be

rendered needless, they would first become very much reduced in size,

and would finally disappear altogether, according to the universal

custom of unnecessary organs. So we should get at length a leafless

plant, with numerous flowers and seeds, just like the dodder.

Parasites, in fact, whether animal or vegetable, always end by becoming

mere reproductive sacs, mechanisms for the simple elaboration of eggs

or seeds. This is just what has happened to the dodder before me.

The other queer plant here is a broomrape. It consists of a tall,

somewhat faded-looking stem, upright instead of climbing, and covered

with brown or purplish scales in the place of leaves. Its flowers

resemble the scales in colour, and the dead-nettle in shape. It is, in

fact, a parasitic dead-nettle, a trifle less degenerate as yet than the

dodder. This broomrape has acquired somewhat the same habits as the

other plant, only that it fixes itself on the roots of clover or broom,

from which it sucks nutriment by its own root, as the dodder does by

its stem-suckers. Of course it still retains in most particulars its

original characteristics as a dead-nettle; it grows with their upright

stem and their curiously shaped flowers, so specially adapted for

fertilisation by insect visitors. But it has naturally lost its leaves,

for which it has no further use, and it possesses no chlorophyll, as

the mistletoe does. Yet it has not probably been parasitic for as long

a time as the dodder, since it still retains a dwindling trace of its

leaves in the shape of dry purply scales, something like those of young

asparagus shoots. These leaves are now, in all likelihood, actually

undergoing a gradual atrophy, and we may fairly expect that in the

course of a few thousand years they will disappear altogether. At

present, however, they remain very conspicuous by their colour, which

is not green, owing to the absence of chlorophyll, but is due to the

same pigment as that of the blossoms. This generally happens with

parasites, or with that other curious sort of plants known as

saprophytes, which live upon decaying living matter in the mould of

forests. As they need no green leaves, but have often inherited leafy

structures of some sort, in a more or less degenerate condition, from

their self-supporting ancestors, they usually display most beautiful

colours in their stems and scales, and several of them rank amongst our

handsomest hot-house plants. Even the dodder has red stalks. Their only

work in life being to elaborate the materials stolen from their host

into the brilliant pigments used in the petals for attracting insect

fertilisers, they pour this same dye into the stems and scales, which

thus render them still more conspicuous to the insects' eyes. Moreover,

as they use their whole material in producing flowers, many of these

are very large and handsome; one huge Sumatran species has a blossom

which measures three feet across. On the other hand, their seeds are

usually small and very numerous. Thousands of seeds must fall on

unsuitable places, spring up, and waste all their tiny store of

nourishment, find no host at hand on which to fasten themselves, and so

die down for want of food. It is only by producing a few thousand young

plants for every one destined ultimately to survive that dodders and

broomrapes manage to preserve their types at all.

XIV.

_DOG'S MERCURY AND PLANTAIN._

The hedge and bank in Haye Lane are now a perfect tangled mass of

creeping plants, among which I have just picked out a queer little

three-cornered flower, hardly known even to village children, but

christened by our old herbalists 'dog's mercury.' It is an ancient

trick of language to call coarser or larger plants by the specific

title of some smaller or cultivated kind, with the addition of an

animal's name. Thus we have radish and horse-radish, chestnut and

horse-chestnut, rose and dog-rose, parsnip and cow-parsnip, thistle and

sow-thistle. On the same principle, a somewhat similar plant being

known as mercury, this perennial weed becomes dog's mercury. Both, of

course, go back to some imaginary medicinal virtue in the herb which

made it resemble the metal in the eyes of old-fashioned practitioners.

Dog's mercury is one of the oddest English flowers I know. Each blossom

has three small green petals, and either several stamens, or else a

pistil, in the centre. There is nothing particularly remarkable in the

flower being green, for thousands of other flowers are green and we

never notice them as in any way unusual. In fact, we never as a rule

notice green blossoms at all. Yet anybody who picked a piece of dog's

mercury could not fail to be struck by its curious appearance. It does

not in the least resemble the inconspicuous green flowers of the

stinging-nettle, or of most forest trees: it has a very distinct set of

petals which at once impress one with the idea that they ought to be

coloured. And so indeed they ought: for dog's mercury is a degenerate

plant which once possessed a brilliant corolla and was fertilised by

insects, but which has now fallen from its high estate and reverted to

the less advanced mode of fertilisation by the intermediation of the

wind. For some unknown reason or other this species and all its

relations have discovered that they get on better by the latter and

usually more wasteful plan than by the former and usually more

economical one. Hence they have given up producing large bright petals,

because they no longer need to attract the eyes of insects; and they

have also given up the manufacture of honey, which under their new

circumstances would be a mere waste of substance to them. But the dog's

mercury still retains a distinct mark of its earlier insect-attracting

habits in these three diminutive petals. Others of its relations have

lost even these, so that the original floral form is almost completely

obscured in their case. The spurges are familiar English roadside

examples, and their flowers are so completely degraded that even

botanists for a long time mistook their nature and analogies.

The male and female flowers of dog's mercury have taken to living upon

separate plants. Why is this? Well, there was no doubt a time when

every blossom had both stamens and pistil, as dog-roses and buttercups

always have. But when the plant took to wind fertilisation it underwent

a change of structure. The stamens on some blossoms became aborted,

while the pistil became aborted on others. This was necessary in order

to prevent self-fertilisation; for otherwise the pollen of each

blossom, hanging out as it does to the wind, would have been very

liable to fall upon its own pistil. But the present arrangement

obviates any such contingency, by making one plant bear all the male

flowers and another plant all the female ones. Why, again, are the

petals green? I think because dog's mercury would be positively injured

by the visits of insects. It has no honey to offer them, and if they

came to it at all, they would only eat up the pollen itself. Hence I

suspect that those flowers among the mercuries which showed any

tendency to retain the original coloured petals would soon get weeded

out, because insects would eat up all their pollen, thus preventing

them from fertilising others; while those which had green petals would

never be noticed and so would be permitted to fertilise one another

after their new fashion. In fact, when a blossom which has once

depended upon insects for its fertilisation is driven by circumstances

to depend upon the wind, it seems to derive a positive advantage from

losing all those attractive features by which its ancestors formerly

allured the eyes of bees or beetles.

Here, again, on the roadside is a bit of plantain. Everybody knows its

flat rosette of green leaves and its tall spike of grass-like blossom,

with long stamens hanging out to catch the breeze. Now plantain is a

case exactly analogous to dog's mercury. It is an example of a degraded

blossom. Once upon a time it was a sort of distant cousin to the

veronica, that pretty sky-blue speedwell which abounds among the

meadows in June and July. But these particular speedwells gave up

devoting themselves to insects and became adapted for fertilisation by

the wind instead. So you must look close at them to see at all that the

flowering spike is made up of a hundred separate little four-rayed

blossoms, whose pale and faded petals are tucked away out of sight flat

against the stem. Yet their shape and arrangement distinctly recall the

beautiful veronica, and leave one in little doubt as to the origin of

the plant. At the same time a curious device has sprung up which

answers just the same purpose as the separation of the male and female

flowers on the dog's mercury. Each plantain blossom has both stamens

and pistils, but the pistils come to maturity first, and are fertilised

by pollen blown to them from some neighbouring spike. Their feathery

plumes are admirably adapted for catching and utilising any stray

golden grain which happens to pass that way. After the pistils have

faded, the stamens ripen, and hang out at the end of long waving

filaments, so as to discharge all their pollen with effect. On each

spike of blossoms the lower flowerets open first; and so, if you pick a

half-blown spike, you will see that all the stamens are ripe below, and

all the pistils above. Were the opposite arrangement to occur, the

pollen would fall from the stamens to the lower flowers of the same

stalk; but as the pistils below have always been fertilised and

withered before the stamens ripen, there is no chance of any such

accident and its consequent evil results. Thus one can see clearly that

the plantain has become wholly adapted to wind-fertilisation, and as a

natural effect has all but lost its bright-coloured corolla.

Common groundsel is also a case of the same kind; but here the

degradation has not gone nearly so far. I venture to conjecture,

therefore, that groundsel has been embarked for a shorter time upon its

downward course. For evolution is not, as most people seem to fancy, a

thing which used once to take place; it is a process taking place

around us every day, and it must necessarily continue to take place to

the end of all time. By family the groundsel is a daisy; but it has

acquired the strange and somewhat abnormal habit of self-fertilisation,

which in all probability will ultimately lead to its total extinction.

Hence it does not need the assistance of insects; and it has

accordingly never developed or else got rid of the bright outer

ray-florets which may once have attracted them. Its tiny bell-shaped

blossoms still retain their dwarf yellow corollas; but they are almost

hidden by the green cup-like investment of the flower-head, and they

are not conspicuous enough to arrest the attention of the passing

flies. Here, then, we have an example of a plant just beginning to

start on the retrograde path already traversed by the plantain and the

spurges. If we could meet prophetically with a groundsel of some remote

future century, I have little doubt we should find its bell-shaped

petals as completely degraded as those of the plantain in our own day.

The general principle which these cases illustrate is that when flowers

have always been fertilised by the wind, they never have brilliant

corollas; when they acquire the habit of impregnating their kind by the

intervention of insects, they almost always acquire at the same time

alluring colours, perfumes, and honey; and when they have once been so

impregnated, and then revert once more to wind-fertilisation, or become

self-fertilisers, they generally retain some symptoms of their earlier

habits, in the presence of dwarfed and useless petals, sometimes green,

or if not green at least devoid of their former attractive colouring.

Thus every plant bears upon its very face the history of its whole

previous development.

XV.

_BUTTERFLY PSYCHOLOGY._

A small red-and-black butterfly poises statuesque above the purple

blossom of this tall field-thistle. With its long sucker it probes

industriously floret after floret of the crowded head, and extracts

from each its wee drop of buried nectar. As it stands just at present,

the dull outer sides of its four wings are alone displayed, so that it

does not form a conspicuous mark for passing birds; but when it has

drunk up the last drop of honey from the thistle flower, and flits

joyously away to seek another purple mass of the same sort, it will

open its red-spotted vans in the sunlight, and will then show itself

off as one among the prettiest of our native insects. Each thistle-head

consists of some two hundred separate little bell-shaped blossoms,

crowded together for the sake of conspicuousness into a single group,

just as the blossoms of the lilac or the syringa are crowded into

larger though less dense clusters; and, as each separate floret has a

nectary of its own, the bee or butterfly who lights upon the compound

flower-group can busy himself for a minute or two in getting at the

various drops of honey without the necessity for any further change of

position than that of revolving upon his own axis. Hence these

composite flowers are great favourites with all insects whose suckers

are long enough to reach the bottom of their slender tubes.

The butterfly's view of life is doubtless on the whole a cheerful one.

Yet his existence must be something so nearly mechanical that we

probably overrate the amount of enjoyment which he derives from

flitting about so airily among the flowers, and passing his days in the

unbroken amusement of sucking liquid honey. Subjectively viewed, the

butterfly is not a high order of insect; his nervous system does not

show that provision for comparatively spontaneous thought and action

which we find in the more intelligent orders, like the flies, bees,

ants, and wasps. His nerves are all frittered away in little separate

ganglia distributed among the various segments of his body, instead of

being governed by a single great central organ, or brain, whose

business it always is to correlate and co-ordinate complex external

impressions. This shows that the butterfly's movements are almost all

automatic, or simply dependent upon immediate external stimulants: he

has not even that small capacity for deliberation and spontaneous

initiative which belongs to his relation the bee. The freedom of the

will is nothing to him, or extends at best to the amount claimed on

behalf of Buridan's ass: he can just choose which of two equidistant

flowers shall first have the benefit of his attention, and nothing

else. Whatever view we take on the abstract metaphysical question, it

is at least certain that the higher animals can do much more than this.

Their brain is able to correlate a vast number of external impressions,

and to bring them under the influence of endless ideas or experiences,

so as finally to evolve conduct which differs very widely with

different circumstances and different characters. Even though it be

true, as determinists believe (and I reckon myself among them), that

such conduct is the necessary result of a given character and given

circumstances--or, if you will, of a particular set of nervous

structures and a particular set of external stimuli--yet we all know

that it is capable of varying so indefinitely, owing to the complexity

of the structures, as to be practically incalculable. But it is not so

with the butterfly. His whole life is cut out for him beforehand; his

nervous connections are so simple, and correspond so directly with

external stimuli, that we can almost predict with certainty what line

of action he will pursue under any given circumstances. He is, as it

were, but a piece of half-conscious mechanism, answering immediately to

impulses from without, just as the thermometer answers to variations of

temperature, and as the telegraphic indicator answers to each making

and breaking of the electric current.

In early life the future butterfly emerges from the egg as a

caterpillar. At once his many legs begin to move, and the caterpillar

moves forward by their motion. But the mechanism which set them moving

was the nervous system, with its ganglia working the separate legs of

each segment. This movement is probably quite as automatic as the act

of sucking in the new-born infant. The caterpillar walks, it knows not

why, but simply because it has to walk. When it reaches a fit place for

feeding, which differs according to the nature of the particular larva,

it feeds automatically. Certain special external stimulants of sight,

smell, or touch set up the appropriate actions in the mandibles, just

as contact of the lips with an external body sets up sucking in the

infant. All these movements depend upon what we call instinct--that is

to say, organic habits registered in the nervous system of the race.

They have arisen by natural selection alone, because those insects

which duly performed them survived, and those which did not duly

perform them died out. After a considerable span of life spent in

feeding and walking about in search of more food, the caterpillar one

day found itself compelled by an inner monitor to alter its habits.

Why, it knew not; but, just as a tired child sinks to sleep, the gorged

and full-fed caterpillar sank peacefully into a dormant state. Then its

tissues melted one by one into a kind of organic pap, and its outer

skin hardened into a chrysalis. Within that solid case new limbs and

organs began to grow by hereditary impulses. At the same time the form

of the nervous system altered, to suit the higher and freer life for

which the insect was unconsciously preparing itself. Fewer and smaller

ganglia now appeared in the tail segments (since no legs would any

longer be needed there), while more important ones sprang up to govern

the motions of the four wings. But it was in the head that the greatest

changes took place. There, a rudimentary brain made its appearance,

with large optic centres, answering to the far more perfect and

important eyes of the future butterfly. For the flying insect will have

to steer its way through open space, instead of creeping over leaves

and stones; and it will have to suck the honey of flowers, as well as

to choose its fitting mate, all of which demands from it higher and

keener senses than those of the purblind caterpillar. At length one day

the chrysalis bursts asunder, and the insect emerges to view on a

summer morning as a full-fledged and beautiful butterfly.

The Evolutionist at Large · 第 5 / 11 段